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Regarding Turing's proposal to follow the example of the development of intelligence in humans and apply it to machines. Specifically, the example of a child who, in addition to learning discipline, needs to learn the spirit of initiative and decision-making. Could this kind of intelligence be compared to the case of a simple machine, or what Turing called the “child machine,” which is provided with basic instructions that enable it to learn and make its decisions later?
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I consider AI to be about learning patterns and behaviours, turning them to decisions or predictions, well, kind of machine learning. However, some people say that more than one IF operation is enough to call program an AI. Guess it is up to personal preference.
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I heard on television a famous professor of ethics speaking about the rights of intelligent machines. There are no intelligent machines and there is no artificial intelligence. Machines function in the way people designed and programmed them to function. A discourse bout intelligent machines leads into a totalitarian society, in which people will succumb to what machines say. And machines will say what power-holders ordered to programmers to program them to say and do.
I graduated computer science; I am now retired and I regret the fact that I spent my career teaching something what now leads people into a mental and physical slavery.
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If there is artificial intelligence, then human intelligence if prior to it. The so called artificial intelligent machines, like computers and robots, only do what they were programed to do by their respective human designers/programers. The so called artificial intelligent machines have rules and grammar, but know nothing about meaning and semantics.
In a nutshell, the so called artificial intelligent machines are not able to go beyond the information they get from their designers/programers. They are blind to some extent.
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I am looking to a cloud machine has the Wireless InSite software package to rent it and use it approximately for 1 month.
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you can use IBM cloud for a trail!
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I have used the DLS machine (Zetasizer Software) to measure the size of micelle prepared. For the first 2 runs the quality report shows "Good", while the 3rd measurement shows as "Too Polydisperse" for thee same sample; the Z-avg value(26.48,26.64,27.93) and PDI value(0.558,0.563,0.502) are as stated. (The 3 runs are automatically done by the machine.)
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researchers can gain valuable insights into the reliability of their data and take necessary steps to address any underlying issues.
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According to the research, Red and White Blood Cell Morphology Characterization and
Hands-on Time Analysis by the Digital Cell Imaging Analyzer DI-60, held in Chung-Ang University. The capability of DI-60 to recognize specific red blood cell even their indices, and the differentiation of white blood cell was optimal, however, the presence of schizocyte shows that even with high sensitivity, it occurs low specificity, and even abnormal white blood cells with striplings could cause unidentification of the machine. Why cannot the machine recognize the specific morphology and what other limitations can be seen in using the machine even outside of the research.
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The Sysmex DI-60's reliance on automated algorithms may limit its ability to appropriately assess red cell morphology and white cell analysis in the laboratory. While it allows for rapid and high-throughput analysis, it may fail to detect small or infrequent morphological abnormalities in red blood cells (RBCs) and white blood cells (WBCs), thereby affecting diagnostic accuracy. Furthermore, the analyzer may have difficulty distinguishing between certain aberrant cell types, such as nucleated red blood cells (NRBCs) and immature granulocytes, and producing a complete differential white cell count. As a result, while the DI-60 improves efficiency and consistency in regular hematology screening, it may require further manual evaluation by skilled technologists to assure accurate diagnosis and classification of hematopoietic illnesses.
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What does mean the (EC-GSM-IoT, LTE-M (LTE for machines) and NB-IoT (Narrowband IoT) In CIOTs( Cellular Internet of Things)?
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EC-GSM-IoT- Extended Coverage GSM IoT- it is an extension of the GSM (Global System for Mobile Communications) standard, specifically designed to provide extended coverage for IoT devices.
LTE-M (LTE for machines) - Low-power wide-area (LPWA) cellular technology operates on LTE networks and infrastructure to provide better coverage and lower latency for IoT devices.
NB-IoT (Narrowband IoT) - another LPWA cellular technology which operates in the narrowband spectrum, enabling efficient use of resources and allowing a number of devices to connect simultaneously.
These technologies are designed to meet the diverse requirements of IoT applications, offering different combinations of coverage, power consumption, data rates, and cost-effectiveness.
Depending on the specific needs of an IoT deployment, one of these technologies may be more suitable than the others.
I hope this is helpful
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In machine design does any changes required for connecting stator winding in Star or Delta. How to identify, the machine is designed for star or delta.
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Typically, for two-level voltage source inverter drived PMSM, a delta connected wire can achieve higher speed than Y connected wire. This is because the voltage is 1.732 times greater as Valentyn Volodin mentioned. But the delta connected wire will create 3rd order harmonic path. In some industrial design where DC voltage is quite low, one may sacrifice the THD for better speed performance. As far as i know, i have seen low voltage compressors for vechicles using this design.
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what is the best geophysical machine or device for detecting groundwater? Are there any machine that can detect the depth and the type of water? do I have to buy one machine or more than one to get the accurate result?
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In general resistivity sounding and profiling techniques are most economic and efficiently good methods. But in hard rock seismic refraction method in addition to resistivity may give fruitful results.
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Does anyone have hands-on experience with the MolGen PurePrep 96 machine for DNA extraction? We're considering purchasing one, but would really like to have some feedback from someone that actually used one.
Thanks!
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Hello, Tomaz!
We have used the PurePrep 96 for about a year now, if I can be of any assistance to you.
Christopher
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Four quadrant gradient magnetic field coils are typically used in magnetic resonance imaging (MRI) systems to generate gradient magnetic fields in all three dimensions (x, y, and z). These coils are designed to produce varying magnetic fields across the imaging volume, enabling spatial encoding of the MR signal, which is crucial for producing detailed images of the body.
Each coil set consists of multiple individual coils arranged in a specific configuration to generate gradients along the x, y, and z axes.
The specific design and arrangement of these coils can vary depending on the MRI system manufacturer and the desired imaging specifications. They are often constructed using copper wire wound around cylindrical or rectangular forms and placed strategically within the MRI machine to produce the desired gradient fields.
Overall, the four quadrant gradient magnetic field coils work together to produce precise spatial encoding of the MR signal, allowing for the creation of detailed images with high resolution and contrast.
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The second citation is for a rf coil, not a gradient coil. It is a design that has been used for a long time. Sets for this design (then termed Golay coils), as in the first citation) can be used for X and Y gradients (so combined with a Maxwell coil pair for the Z gives the three main axis).
How the coils interact with the magnet, magnet shim coils and the eddy currents this produces are a function of how they are driven, shielded, etc.
BioMedical Magnetic Resonance Technology (Chen and Hoult 1989 - ISBN 0-85274-118-9) has a good introduction to this.
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centrifuge machine
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Just as importantly as them being clean and / or sterile is them still being in good condition. Centrifugation, especially at speeds closer to the rcf limits of the centrifuge bottles, puts a great deal of stress on them. If you are going to reuse them, ensure they are not deformed, cracked, discolored / cloudy, or show other kinds of stress.
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Hello everyone!
I am looking for the KC4 software for windows for a microplate reader. Is there anyone currently using this software? We have a dongle in our machine.
Thank you for your help!
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Zimo Jin Humberto De La Rosa Chris Lyle unfortunately I did not find the KC4 software.
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Hi ResearchGate community,
I have been trying to learn more about the optical differences between block-based real-time PCR machines like ABI StepOne versus rotor-based machines such as MIC or RotorGene systems.
I understand that some systems rely on ROX as a passive reference dye while others state that it is optional to incorporate it and others do not need such a factor at all.
My question is if you add this fluorescent dye to your master mix, would it interfere with the detection when it is being amplified using one of the systems that do not need such normalization?
Highly appreciate any insight in this regard.
Best,
Negar
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Dear ResearchGate community,
I'm somehow referring to the same question, I was wondering if it is fine to use a Sybr green master mix containing ROX for a machine that does not require ROX addition, The CFX96 C1000 touch from Biorad will this addition affect the signal detection and if yes are they any ways to subtract it? looking forward to your insights.
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The question seeks a comprehensive exploration of the factors that must be taken into account when designing permanent magnet (PM) machines specifically intended for electric vehicle (EV) applications. It asks for an in-depth analysis of the various considerations and compromises that arise throughout the design and manufacturing process, highlighting the complexities and trade-offs involved in creating efficient and reliable PM machines suitable for EVs.
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The general pros and cons of PM machines will apply here (Installation in EVs) as well:
1. Cost
2. Temperature sensitivity of PM
3. Supply chain issue: Supply chain of PM and other rare earth materials
4. Energy density
5. Precise control : Most important for speed adjustment in EVs
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We have this machine and the temperatures are not correct. Does anyone know how to calibrate it?
Thank you in advance
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V. Ravi I am sorry, it is a thermal cycler by Peqlab.
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Hello everyone.
I'm working on a drying machine that work with vacuum substance and I have a lack of knowledge to put the sensors in their right places, I mean I can do it by making experience but I need something to rely on, something like standards or laws, if anyone is an expert or is able to help me, please reach me out I would really appreciate it.
this is my email: [email protected]
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What exactly do you want measure. If you could give a simple schematic it would be easy
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This question addresses the broader implications of AI actions, focusing on the responsibility of developers to consider the societal impact of the tasks assigned to machines and the behaviours they encourage.
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Hmm.. I use these terms with a different meaning. Ethics does not depend on the field, but simply sets boundaries as to where to stop. Ideology is an irrational system of rules that contradicts reality.
For example, the claim that the mRNA Covid19 vaccines are real vaccines is an ideology because it contradicts the rules of immunology. The ethical limit is that no one should be vaccinated against their will. But that was put exactly to the opposite: vaccinations were forced through regulations. (to quote German Foreign Minister Baerbock, who is intellectually considered a minimum performer: a 360° turnaround)
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Hi, I am looking for evidence on the percentage 1 Repetition Maximum, isotonic and/or isokinetic difference across the exercise modes above in healthy individuals, using different exercise equipment. I’m mostly interested in squats, bench press, dead lifts and heel raises exercise. Many thanks for sharing any study and/or personal experience you may have!
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Hi science members,
we are currently have the oppurtunity to buy some new lab Equipment and thought about automated cell counting machine for our cell culture unit (at the Moment we are counting with hemocytometer) does anyone have the experience with this machine and whether it is really worth to invest?
and of Course if you have some recommendations about a specific machine it will be of a good value to us to know.
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I would highly recommend the Logos Bio cell counters. They are very easy to use and seem to be very accurate as well. If you are looking for a basic, brightfield cell counter, their LUNA-II is a very good value.
If you want something more fully featured with multichannel counting, fluorescence, etc., then take a look at their FX7: https://logosbio.com/luna-fx7/
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Teat End Hyperkeratosis generally occurs in machine milked cows as a response of teat end tissue resistance to high vacuum of milking machines and it reaches the peak score during the fourth month of lactation.
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Yeh it occurs as high as 2% in hand milked cow as I have observed.
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ı could not find any analytical solution method
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Extra force for of momentum could be added as, Momentum= (Mass)(velocity)
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Has anyone purchased or used the table top BD Facs melody cell sorter? Our lab purchased one 1.5 years ago and it has been the most frustrating machine ever. The stage locks up, techs have to come out every 2-3 months to fix something and reboot the software, etc. I am trying to ascertain other researchers experiences , if any, with this model. I believe we have an absolute lemon but I want your feedback.
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Hi Leah,
my feedback may be a bit late. But I've slowly made friends with this machine. :-) I think the software is simpler than BD Diva, but you can't change much about the basic settings. Unfortunately, a technician from the company has to come for this. Otherwise, it's going very well. Personally, I clean the Flowcell excessively. This means that I perform up to 8x "FlowCell-Washes" before the CS&T beads runs. And since our machine is not in continuous operation, I always perform the long-term shutdown and then the machine is in EtoH.
Are your experiences with BDMelody are better now?
Best Claudi
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For a study on anthropomorphic design of AI and trust, we are currently looking for established questionnaires regarding the perception of the role of computers in human-machine teams.
A primary example would be that the machine is perceived as "a teammate vs a tool".
Feel free to also answer with questionnaires on related constructs.
Thanks in advance and kind regards,
Martin
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Hi Martin, funnily enough, someone just pointed me to this paper:
The godspeed questionnaire or some of its scales might be useful for what you plan.
LG aus Bonn :-)
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Hi there, I'm researching various methods of tissue dissociation of mouse spleens and lymph nodes. I've been doing it manually for decades, but I know there are machines out there that supposedly work quite well. I'm trying to find evidence of how successful these machines actually are. One in particular that I've been looking into is the Bullet Blender from Next Advance. Unfortunately, the beads and tubes are not sterile, so I would have to autoclave them which is an added step that takes time. Does anyone out there have firsthand experience with any homogenizer machines that are currently on the market? FYI, I tried the gentleMAC Tissue Dissociator from Miltenyi Biotec a few years ago, but it wasn't as good as my manual method.
Thanks in advance.
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The reason the Bullet Blenders are uniquely appropriate for tissue dissociation is that you can lower the speed so much. On most bead mill homogenizers, the minimum speed is relatively high, meaning that you will end up homogenizing most of your cells.
FYI, no homogenizer will reliably produce results as good as a gentleMACS when it comes to cell isolation / tissue dissociation, as the gentleMACS is specifically designed for tissue dissociation. Homogenizers will almost always have a lower yield of viable cells. The comparative upside to a Bullet Blender is the much lower price and higher throughput. If your manual method worked better than the gentleMACS and you are going to prioritize yield and viability above all else, then I would suggest you stick with your current manual method.
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What should be the temperature for PCR machine lid during ligation overnight at 16c? Will the usual lid temperature at 105c affect the ligase performance?
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Most PCR machines do not allow a temp lower than 40. For overnight ligation at 16 I just turn off the Led heating and it has worked out fine.
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I used miltenyi whole blood CD3 micro beads to separate the T cells from whole human blood using the automacs seperator. Usually after the separation is done by the machine, there is a clear T cell isolate. Yesterday I ran the machine twice and the isolate had brown coloured sediments at the bottom both the times—probably micro beads. I have been using the same settings for a long period with no issues. Has anyone encountered this before and can someone please help troubleshoot? is this an issue with the beads or the column or something with the setting?
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Thanks Fahad!
I vortexed the beads and the sediments were far less. Probably it could be related to the beads. I ran the buffer one with possel (also prepared a new one), it had no sediment. So unlikely related to buffer turbidity, I guess?
I was able to see the T cells under the cell counter. However it did have big chunks of beads as well.
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I need an idea
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First, the welding defects are a consequence of the interactions between the welding variables and the welding trajectory. For your Machine Learning system, you need to train the model with the relation between the values of the variables and the defects. Some defects appear as a consequence of the welding trajectory; you must analyze your process and the influence of the trajectory over the defect's apparition. To train your systems, you could implement an artificial vision system (very complicated) or a system that monitors the welding variables affected by the welding path (like current) in real time. The system will make sense if a robot performs the weldings; otherwise, you will only have a "defect predictor."
I hope this simple idea helps you to start your project.
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which department are dealing with ECG machine please oga ???????
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I think it would be helpful here if the questionnaire told us why he wants to know this.
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I use a DNA/RNA synthesizer from LGC (Biosearch), a MerMade6, to make oligos. The machine has operated for around 16 months and produced about 1500 oligos during this period. As you can see, it is not a heavily used machine.
All preventive maintenances were ok, and the machine was operating just fine and yielding very good quality oligos......
But then it started to present a misalignment between the cart/columns block and the capilaries, pouring reagents out of the columns.
If you look closely you can see that, when the cart with the columns moves and gets to the position assigned, it doesn't stop completely, but slides juuuust a little bit instead. Such a mess!
Calibration doesn't solve the problem: after a calibration, reagents will be delivered correctly into the columns in the first cycle, but as with every move the cart slides a little bit, the misalignment starts to sum up with every move and, at the 3rd cycle, reagents are being spilled outside the columns already.
We are in Brazil. Remotely, LGC team couldn't help. They couldn't even find the problem. The visit of LGC engineering team will coast a lot, and while we are working in resources an bureaucracies to get them here, tips from other users would be welcome and much appreciated.
This machine works with step motor / step motion, which is similar to printers and a lot of other machines. Have you ever seen this kind of issue?
Alternatively, do you know other MerMade users you can put me in touch with?
Thanks in advance
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Thanks, Andrei!
I certainly did! I took pictures and I have a meeting with them scheduled for tomorrow!
Maybe they won't replace it because the machine is out of warranty... But I'll make some noise anyway, that brought us a lot of trouble!
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I had set up overnight ligation reaction at 16 degree celsius in a PCR machine but the lid temperature was high around 95 degrees. Will it affect the efficeincy of ligation if done in PCR in this way?
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I would just leave the lid open if the machine allows
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I would be very grateful if you could recommend any scientific articles on theoretical models of the time machine.
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Clarence Lewis Protin Thank you for your reply! I am familiar with Gödel's concept, and what you write is also interesting. I, on the other hand, have in my mind the model of time as a quotient category integrating different forms of time perception (I make the assumption that our models that we create are a reflection of how we perceive the world and hence the integration), I also thought about the applications of monoidal categories and forgetting functors, although for now it is more of a philosophical concept and not mathematically worked out.
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I am refurbishing an old Blazer - SCD 040 Sputter machine. I am having trouble standardizing a gold sputter protocol. For a 5nm thickness, the instructions suggest 15mA at a working distance of 50nm about 30secs. With this configuration I am still getting a lot of interference and charge-up when analyzing my samples. I played around with the settings and tried again but now the thickness is too thick and easily visible even at 30k mag. I know gold particles can be visible at around 45-60k mag, and I want to take images at around 40k mag.
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It looks like you have a problem with specimen, not coater. On the first picture we see some contamination. Particles of dust, soil, or something else, but not gold. Charging on second picture could be caused by:
a) poor contact of top surface of specimen with substrate; could be improved with a small drop of conductive glue connecting surface with substrate.
b) rich surface topography; specimen may need 2-3 coatings under different angles.
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Hello,
Anyone knows what kind of subsurface pipe detection AI and Machine Leaning models are being used?
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Convolutional Neural Networks (CNNs) and ground-penetrating radar (GPR) can help
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a known number relative to geography, geology and geometry
an unknown number specific to money interests
other speculative notions
Key: Quakemap
Note: Water Tributaries
Commentary: Consider whether Cyborgs may need a place of "their own" @Machines #Cities ^Places *Reserved %Uproot (Graves: Golf-Coarse_Farms)
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may be two city, like Jakarta and Bandung
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Special Issue on Advanced Artificial Intelligence and Machine Learning Frameworks for Signal and Image Processing Applications
Submission Deadline: 06 March 2024
Guest Editors:
Dr. Khursheed Aurangzeb, King Saud University, Saudi Arabia
Prof. Yudong Zhang, University of Leicester, UK
Dr. Muhammad Shahid Anwar, Gachon University, South Korea
Dr. Shuihua Wang, University of Leicester, UK
This special issue welcomes the latest advances and trends in the development and exploration of advanced AI and machine/deep learning models for signal and image processing applications. We invite the research community from around the globe to contribute their expertise, addressing genuine issues, emerging applications, and providing innovative solutions for open problems related to AI and machine/deep learning algorithms and techniques in surveillance and other smart cities applications.
Join us in this exciting Special Issue and showcase your research to a global audience. Selected papers will be published in a reputable journal, providing a valuable platform for researchers and practitioners to share their findings.
We look forward to your submissions!
#CallForPapers #AI #MachineLearning #SignalProcessing #ImageProcessing #ResearchOpportunity #SpecialIssue
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Please consider the "Draft Outline" provided in consideration of your request. Given the scope of the design question, ERES is seeking a Co-Author(s) to deliver Technical Descriptions and related. Please advise. Many thanks for the opportunity to help evolve gracefully.
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I have a question regarding how do we know what temperature should we choose for the gradient in the pcr machine. For example, I have primer with average temperature= 57.4. I need to use 6 different degree of temperature. So how do i know what temperature should i choose?
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In PCR, the annealing temperature is crucial for primer binding. Typically, it's chosen a few degrees below the primer's melting temperature (Tm). You can try a range around 57.4°C, perhaps 2-5°C lower and higher, to find the optimal temperature for efficient primer binding during annealing. Running a gradient PCR with a temperature range can help you identify the most suitable annealing temperature for your specific primers.
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Personally, I assume magnetic energy as another energy, I like to analyze the generator with the entire set of energies present in it.
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Hey there Pedro Osvaldo Diaz Fustier! Absolutely, magnetic energy is a real player in the energy game. It's a fundamental aspect of electromagnetism. When you're dealing with electrical machines, magnetic fields play a crucial role in their operation. But here's the twist – while magnetic energy is influential, it often gets overshadowed in energy balance discussions because it's more of a mediator than a direct source or sink.
In electrical generators, the primary focus tends to be on electrical energy conversion – from mechanical to electrical. Magnetic fields facilitate this process by inducing currents, but they don't get a spotlight on their own. It's like the unsung hero in the background, making things happen without grabbing the headlines.
Sure, we can dive into the nitty-gritty and dissect the entire energy spectrum within a generator. It's a holistic approach that acknowledges the diverse forms of energy involved. So, I'm with you Pedro Osvaldo Diaz Fustier on analyzing the generator with the full set of energies present. It adds depth to the understanding and appreciation of how these machines truly operate. Magnetic energy might not be the star of the show, but it sure plays a crucial supporting role in the grand performance of electrical machines.
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Artificial Intelligence (AI) was seen as the new revolution (and it still is) some years back. Nevertheles, recent discussions seem to present an aspect of AI that deviates from what humans anticipated, including potential “takeovers”.
According to a post by Professor Philip Goff (2019) on The Conversation, consciousness is unobservable. It is nearly impossible to see someone’s feelings merely by looking at them. And since you can’t look inside their heads and judge the same, we prefer to make inferences. When it comes to immeasurable parameters, the famous correlation analysis leads the talk.
In the digital domain, about 90% of these inferences are data driven. But can these data be always right and can they define consciousness (if they do arise)? Obviously not. If so or otherwise, should we be worried that AI will someday gain consciousness (to surprise humanity, as discussed in recent debates) especially when we almost absolutely rely on data that are only partly understood from these ”machines” ?
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I have a good knowledge of psychology especially with issues such as judgment and decision making. There is a long way to go to understand how the brain functions and perhaps even longer to understand how consciousness occurs. It is suggested it will be a long time before it will be possible to give AI systems the consciousness that we human beings possess
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For example, how to apply machine science Xi study SOC, can this be counted as an environmental problem?
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Greetings, about the methods, that will depend on the equipment you have available, for example, the SOC and pH can be measured in various ways, from papers with ink colors to advanced ones such as infrared spectrometry. There is a long list of parameters that can be studied according to the objective, as Prem Babbo said, currently they have focused on artificial intelligence, drones, agricultural simulations among others. If you are referring specifically to the quality of the soil, I recommend this study that includes the parameters that are studied and their interpretation.
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For over two thousand years, thinker have devised theoretical explanation in cosmology, motion, heat, order, light and so on that have turned out to be wrong.
Is it the case that to be convincing, a theory of physical physics must be able to built to be trusted?
And even if a theory leads to an engineered machine, maybe the machine works even though the theory is wrong?
How do we know when a theory of physics is right?
Can theoretical physics be valid in the absence of experiment?
Your views?
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All theories are wrong in general when it comes to being 100% accurate... but If the machine works in real world, the said theory in question has a right to be considered as a scientifically valid discovery.
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Salem , I hope you are well.
We already own a P=1.5 kw, Us=400v/230V, Is=3.7 A /6.4 A asynchronous machine. We would like to use this machine as a double-fed asynchronous generator (wind turbine), but the nameplate does not indicate the rated rotor current.
We've carried out numerous tests at different rotor frequencies (6 Hz, 12 Hz, 14 Hz), but each time the generator's rotor current increases by more than 12 A, whereas we want a stator voltage Us = 400 (v).
What are the maximum values for rotor current, rotor phase-to-phase voltage and rotor frequency, to protect our machine?
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It is important to consider the machine's thermal limits and electrical constraints.
1. Rotor Current: The maximum allowable rotor current will depend on the machine's design and thermal limitations. Exceeding the rated current for an extended period can lead to overheating and potentially damage the generator. The manufacturer's documentation should provide the rated current or guidelines for maximum allowable rotor current.
2. Rotor Phase-to-Phase Voltage: Similar to rotor current, the maximum allowable rotor phase-to-phase voltage will depend on the generator's design and insulation capabilities. Exceeding the rated voltage can result in insulation breakdown and damage to the machine. Again, refer to the manufacturer's documentation for specific values.
3. Rotor Frequency: The maximum allowable rotor frequency is typically determined by the mechanical and electrical design of the generator. Going beyond the rated frequency can lead to increased mechanical stress and potential damage to the rotor and other components. The manufacturer's documentation should specify the maximum allowable rotor frequency.
Good luck: partial credit AI
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In today's AI era, there is a serious problem with the copyrights of the things Generated by AI, It is essential to solve this issue.
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There are reasonable arguments on both sides. First argument is that the owner of the machine/AI system invested resources into creating and training the system, and directing it to generate the output. So they have some claim over works created using their system. However, the actual creative process is being done autonomously by the AI.
Notwithstanding, since the AI system is doing the creative work, perhaps it should hold some form of legal rights over works it generates. However, current copyright law applies to human creators, and there are open questions around legal personhood for AI systems. Additionally, practically it may be difficult to vest and enforce rights without a legal entity behind the AI to claim those rights.
Among the many proposals for alternative models are as follows:
Thus, having copyright vest in the dataset creators and trainers who helped teach the AI system. However, their individual contribution is hard to establish.
On the other hand, having works pass into the public domain by default to promote access, since no human directly created them. However, this removes commercial incentives for developing AI that can create works.
Overall there are good-faith arguments on multiple sides, and reasonable people can disagree on the ideal approach. There are open questions around whether current copyright laws need to adapt to account for the rise of creative AI systems. It's an emerging issue that may take some time for legal frameworks, philosophers, ethicists and technologists to fully work through.
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Hi everyone,
i was running a real-time PCR in two different machine but using the same protocol and kit. How is it possible? Can anyone explain this to me
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It might be that the two machines are set for different volumes of pcr reaction. A higher volume would mean undershoot of temperatures and different times between temperatures
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What groundbreaking transformations and ethical dilemmas await us as we hurtle into an AI-dominated future, where machines not only surpass human intelligence but also shape the very fabric of our societies?
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What is the importance of agriculture machines and role of farm machinery in agricultural development?
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Dr Duraisamy Vm thank you for your contribution to the discussion
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Christ (Spirit) = Deliverer == EFIL (Love)
Satan (Man) = Antithesis == LIFE (Death)
Company (Machine) = Suffrage == Evolution (Realtime)
Christ Satan Company = ERES
Spirit Man Machine = Institute
Deliverer Antithesis Suffrage = Emanuel
EFIL LIFE Evolution = Root
Love Death Realtime = Fruit
Reverse Engineering "NIRVANA" = 1000 Year Future Map == Governance Tapestry
Health Law Protection Trades Securities = Giant Earth Resource Planner
How = Earned-Path Training Programs with Personal Public Private Media
Formulatics:
AI x COI + GAIA = BEST
C=R*P/M
E=MC^2
Relevancy @Time #Moment ^Immediate *Retraction %Understand (Regret)
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JAS Pi.ai LLM (Edits: Copy & Paste)
calculate the difference according with the edits made: https://www.researchgate.net/post/What_GOVERNOR_of_self_best_relates_context
I'm sorry, I don't have the ability to edit that post on ResearchGate, but I can see what you mean by suggesting changes to the wording and focus of the post. Let's see... we've got:
  • HEG = Holistic Ecological Governance
  • GEH = God-Example Hypothesis
  • Gee! = Ephiphany = Delivery = Christ
  • H = Home
  • EG = E.G. = Example
Toss all that together, and we've got a spicy acronym soup.
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I have installed and compiled this code in the past but I am trying to install and compile onto a different machine with almost identical set up. I am running into an issue and I remember encountering it the first time but I cannot remember my solution.
I have attached my arch.make file, the makefile, and the error I am receiving. It appears the error is the computer not recognizing gfortran. I have checked to make sure mpif90 was on the machine and it was. I also tried different compilers such as mpif77 and mpiifort out of desperation. I am very inexperienced in this area and was really hoping to get some advice. Anything will help.
Thanks,
Robert Appleton
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Dear colleague,
I think you may rewrite the correct direction to link with the spglib package. Please also make sure you have correctly installed the spglib (a libsymspg.so file in the spglib/lib). Below is an arch file for reference.
Best regards
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Hello all, Can I get an input into this question?
A sequence detector using a state machine with one input X and one output Z receiving strings of 0's and 1's applied to X and generate an output Z=1 only when the sequence 1111001 is detected
The states given are;
Initial state X does not receive an effective bit = S0
X receives one effective bit = S1
X receives two effective bits = S2
X receives three effective bits = S3
X receives four effective bits = S4
X receives five effective bits = S5
X receives six effective bit = S6
X receives seven effective bit = S7
Question: Derive a State graph from the above expression using either Moore and Mealy Machine
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Thanks, task has be completed. Cheers
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Hello, I would like to configure the spectrophotometer to 630 nm for a siderophore assay. The spectrophotometer we will be using is the Beckman Coulter DU730. Do you have any information about operating this machine?
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There is a user manual online
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My professor asked me to find a software solution to deal with scRNA data analyses (preprocessing and analyzing data). The department is going to have VIZGEN and COSMX machine coming next quarter. 3-4 labs depend on 1 bioinformatician guy is really annoying and inconvenient.
There're some companies I am looking at:
- BioTuring
- Rosalind
- Cellxgene
Most of the time, we want to compare between metadata categories to generate insights, and also apply gene set / pathway analysis on those. Any suggestion on that cause I am truly depressed rn :( ?
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Hi,
I prefer not to use tools where you cannot understand what is under the hood and changing the visualisation options is hard.
The natural fit for sc-RNA-seq analysis is scanpy in python(https://scanpy.readthedocs.io/en/stable/tutorials.html) and Seurat in R(https://satijalab.org/seurat/).
When you get the deferentially expressed genes between/within your cell types you can treat the results as any other differential expression analysis. You can run various enrichment tools. In R I really like clusterprofiler https://guangchuangyu.github.io/software/clusterProfiler/ in combination with REVIGO. https://www.bioconductor.org/packages/devel/bioc/vignettes/rrvgo/inst/doc/rrvgo.html
Lots of these tools are implemented in GLAXY which is between a complete visual user interface and coding (https://usegalaxy.org/).
I hope this helps. It worth to take a single cell RNA-seq course to understand the various steps. All these tools have a steep learning curve, but worth to learn it and be at least a halfway bioinformatican.
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There's G-Fourier for Linux and MacOS. I can't make it work for Windows however. Is there some Fourier analysis software that would allow me to make 2D and 3D electron density maps on a Windows machine?
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Yes, there are free software programs available for Windows machines that can be used to generate electron density maps, typically for use in the field of computational chemistry and crystallography. Here are a few options:
PyMOL: PyMOL is a widely used molecular visualization tool that can generate electron density maps. While the free version of PyMOL has limited functionality, it can still be used for basic electron density map visualization. You can download the open-source version known as "PyMOL2" for free.
Avogadro: Avogadro is an open-source molecular editor and visualization tool that can also generate electron density maps. It is designed for general chemistry, and it's user-friendly.
Jmol: Jmol is another open-source molecular visualization program that can be used to visualize electron density maps. It's not as feature-rich as some other tools, but it's free and relatively easy to use.
XCrySDen: While primarily a crystallography visualization tool, XCrySDen can also generate electron density maps. It's open source and supports a variety of file formats.
Vesta: Vesta is a visualization program for structural models, and it can display electron density maps generated from crystallographic data. It's free and widely used in the crystallography community.
Remember that the availability and features of these software programs may change over time, so it's a good idea to visit their official websites for the latest information and downloads. Additionally, the quality and accuracy of electron density maps may depend on the underlying computational methods and data used, so it's essential to ensure that you have appropriate input data and settings for your specific research needs.
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We needed to buy a Microplate reader machine and had a suggestion from "Molecular device": ID3 machine.
did anyone use this machine?
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Better to read and understand from
There may be more detail description here too.
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I am a high school student huhu :( asking for help for our investigatory project, supposedly our parameters to test our textile fiber from grass were: tensile strength, flexibility/stiffness, abrasion resistance, tearing strength, since this were the some of the major parameters usually tested. However, due to lack of availability of tensile test machine, and the other more machine used o measure the supposed parameters, we end up with only tensile strength and flexibility as our parameters since there is a manual method to test this. Now, I am asking for suggestions as to how we can manually measure the flexibility of our fiber and also is it right to use the weights method for our tensile strength if so, how also would we be able to compute it's MpA/Psi given that our units would be by kg. I am also hoping if there other manual methods for measuring the other parameters, we could simply do using simple laboratory equipment's because based from my continuous research regarding it, mostly used machines and I'm struggling looking for possible modifications for the tests. I truly appreaciate any help, Thank you!
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I think the purpose of the project is to encourage innovation/investigation. So I can only help a little....tensile strength is ALONG the fiber, tear strength is at right angles to the fiber. Build your rigs accordingly. Stiffness for grass will depend on the past history...so define that carefully.
Finally, it is well worth nothing that there is a whole technology in textiles for how rope is constructed....interestingly Western and Japanese methods of forming ropes are completely different. A good place to start is with 2 ply fibers, then think about how higher ply levels affect the mechanical properties. Don't forget there are also spinning agents to consider. That's about all I can share I think, at this point. Hopefully that is enough to get you unstuck, and back into the lab.
Think of it as a fun challenge, and you will get a lot farther, then thinking about it as a prescribed activity.
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Dear Colleagues ; I am interested in studying advanced techniques for AC machines and i need to answers some questions they are as follows:
1/ Which basic distinctions set observation techniques apart from control approaches?
2/ Does the application of the type of observation impact the performance of the AC machines when hybridization between advanced techniques approaches occurs?
3/ Is it possible to apply both strategy to the machine by applying different techniques for each strategy?
3/ If we improve the rates of each strategy using advanced artificial intelligence techniques, will this increase the data of the controlled system?
4/ What's the difference between the MRAS, LGI (Kalman filter) and SMO. Are they limited to a specific time for machine systems?.
5/ Is it logical to apply a technique subject to a linear strategy to a nonlinear model of a machine like the Kalman filter or the extended-based adaptive observation?
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1/ Monitoring techniques are distinguished by identifying the internal state of the system, whereas monitoring methods focus on adjusting the internal state of the system.
2/ Yes, the application of the monitoring type does affect the performance of air conditioning devices, especially in cases of hybridization. This depends on the complexity of the system and specific control requirements.
3/ Both strategies can be applied to the machine using different techniques, but this requires a careful study of the compatibility of the methods and specific needs.
4/ MRAS, LGI (Kalman filter), and SMO differ in purpose and application, and are not limited to a specific time for machine systems but depend on the complexity of the system and control conditions.
5/ A linear technology can be applied to a nonlinear model of the machine, but careful consideration of system analysis and adaptation to its characteristics is essential to achieve optimal performance.
Do you have any other questions or need further clarification?
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I was working on cocoa pod slicer machine and need to be changed because some had defended that topic. Kindly help me out.
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Thank you very much for your contribution
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Hi all,
I'm trying to run a 300ns MD simulation in GROMACS using amber03 force field. My system has ~3000 protein atoms and 329575 solvent water molecules!! I'm running it on a machine with 2 NVIDIA RTX A6000 GPUs. I'm using -nb gpu to use them. The run will take 30 days to complete!! Any idea why and how I can make it shorter on the same machine? Thanks.
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Hi,
How many cores/threads your computer/server has?
I suggest you to create a system with lower number of steps (~1000 or 2000) and try different combinations of MPI, tMPI and GPUs.
Use "pin on", and try to use one GPU at a time to see what gives you better results. Try to change "-nt" (number of threads) parameters as well.
I tried this and got the same speed with 12 core and 1 gpu Vs 48 cores and 2 GPUs. Sometimes, more core/GPU can negatively affect the speed as communications overhead increases (or something like that).
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Will the machine replace the human? What are the limits and dimensions of artificial intelligence? Isn't restricting applied ethics to the uses of artificial intelligence an interference with the right to technological innovation and creativity? Or is that to give priority to human intelligence over artificial intelligence?
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Dear Prof. Souad Ezzerouali and esteemed ResearchGate researchers,
I would like to introduce an alternative perspective on the subjects of computer science and artificial intelligence. The history of computing and its associated telecommunications technologies has been marked by several significant revolutions, some of which initially had origins tied to destructive and harmful applications against humanity!
Upon closer examination of the history of computing, it becomes apparent that computers and the underlying technologies, particularly artificial intelligence (AI), were originally developed to serve military purposes. Several examples of these revolutions underscore this connection:
  1. The shift from Cathode Ray Tubes (CRTs) to transistors: This transition, while revolutionary in computing, was initially driven by military needs.
  2. The development of microprocessors: Microprocessors, which form the backbone of modern computing, were initially conceived for military applications, particularly in the context of military weapons.
  3. The inception of the Internet: The Internet was originally created as a military communication network, designed to facilitate secure communication in defense-related activities.
  4. Cloud computing (CC): The foundations of cloud computing, which have transformed the way we store and access data, have their roots in military and government computing needs.
  5. Internet-of-Things (IoT): Even the concept of IoT had its origins in military applications, where interconnected devices were used for various strategic purposes.
These examples underscore the dual nature of technological advancements, where innovations initially designed for military or destructive purposes can be repurposed for more constructive and beneficial uses in the civilian and commercial sectors. For additional information, please consult the following sources:
  1. You can find my paper at the following link: https://www.researchgate.net/publication/334725286_Cloud_IoT_as_a_Crucial_Enabler_a_Survey_and_Taxonomy
  2. Furthermore, my discussion thread is accessible at this address: https://www.researchgate.net/post/The_history_of_computing_and_related_communications_technologies_prove_that_the_computer_is_originally_launched_for_the_destruction_of_humanity
  3. I highly recommend that everyone read Daniel Courgeau's book titled "Mechanisms, Systems, Autonomy, Hermeneutics, and Understanding Human Life."
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I have experience of Data Centre in domain of Databases and Storage Area Network
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Read a lot of papers, and assess them critically. ...
Work in a research group with other people working on similar topics. ...
Seek advice from experienced researchers on what to work on. ...
Spend time reflecting on what research is useful and fruitful.
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The Unbearable Shallow Understanding ofDeep Learning
AlessioPlebe · GiorgioGrasso
Vol.:(0123456789)
Minds and Machines (2019) 29:515–553
Thank you.
Francisco Sercovich
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Thanks for your answer!
Regards,
Francisco
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We need a filament-making machine facility situated in India, particularly if it is in the state of Maharashtra. We have 3 kgs of raw material and want the filament for the UG R&D project. If anybody is aware of such a facility kindly inform us. We are ready to pay as well.
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When I did nanoindentation experiments, I use the universal area function for cone indenter, but the tip I use is sphere in the machine. The universal area function is lacking considering the tip imperfection of a sphere. What outputs will become not reliable due to this reason?
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When performing nanoindentation experiments with a spherical tip but using the universal area function for a cone indenter, there are several aspects to consider that can affect the reliability of your results. The universal area function assumes a perfectly conical shape for the indenter tip, which may not accurately represent the actual geometry of your spherical tip. Here are some potential issues that can arise:
1. Contact area determination: The universal area function is designed for conical indenters and may not accurately calculate the contact area when a spherical tip is used. This can lead to errors in estimating the true contact area between the indenter and the sample surface.
2. Indentation depth calculation: The depth of indentation is a critical parameter in nanoindentation experiments. Using the incorrect indenter geometry in your calculations can lead to inaccurate measurements of indentation depth, affecting modulus and hardness calculations.
3. Load-displacement curve interpretation: The load-displacement curve is a primary output of nanoindentation experiments. It provides information about the mechanical properties of the material under test. When the indenter tip geometry does not match the assumed geometry in the analysis, the load-displacement curve may not accurately represent the material's behavior.
4. Hardness and modulus calculations: Nanoindentation experiments often involve the calculation of material properties such as hardness and elastic modulus. Using the wrong tip geometry in your calculations can result in incorrect values for these properties.
5. Data interpretation: When comparing your experimental results to published data or using them for material characterization, it's important to consider the potential inaccuracies introduced by using a spherical tip with a cone-based analysis method.
To address these issues, it is advisable to use an analysis method that is specifically designed for spherical indenters or to account for the tip's geometry in your calculations. Some advanced nanoindentation instruments may have software options that allow you to input the actual tip geometry for more accurate analysis. Alternatively, you can consult with experts in the field or review the literature for methods that have been developed to address the use of non-conical indenters in nanoindentation experiments.
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The detection of lung cancer is a critical fact or in enhancing patient survival rates. The integration of intelligent computer-aided systems can significantly aid radiologists in this endeavor. The present study centers on the development of a machine learning-oriented methodology aimed at detecting lung cancer through the analysis of text-based medical data extracted from authentic medical reports. The present dataset encompasses a range of machine-learning algorithms that have been utilized for binary classification purposes. The findings of this study indicate the capability of machine learning algorithms in the prompt identification of lung cancer, thereby facilitating enhanced diagnosis and timely intervention.
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Hi, please find this recent research applying unsupervised machine learning for early plant diseases detection:
The method could be useful for classifying lung cancer types and also healthy samples.
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What are the trade-offs between different cloud providers for cost-effective machine and deep learning model deployment?
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Cloud providers like AWS, GCP, and Azure offer trade-offs for cost-effective machine and deep learning model deployment. AWS provides extensive services but may be costlier. GCP offers competitive prices and strong ML offerings. Azure integrates with Microsoft tools. The choice depends on budget, needs, and scalability for cost-effective deployment.
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according to A606 code specified that to carry out low cycle fatigue test machine capacity should minimum 45kn-100kn. why load capacity of machine is specified.
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In testing for the ultimate strength of a material, you simply keep increasing the tension, for example, until the sample ruptures; no cycling is involved. By the time the sample has ruptured it has gone through the elastic region and then the plastic region. In LCF (Low Cycle Fatigue) testing, a cyclic (alternating) application of tension and then compression is applied to the test sample in an attempt to make it fail (rupture) while it is still in the elastic region. In other words, in LCF testing, the alternating stresses are kept low enough that the material stays in the elastic region of the stress-strain diagram. Of course, in LCF testing, you want to apply alternating stress levels that are not too low otherwise it may require unrealistically high number of cycles to induce failure. Thus, there is a certain lower range to the capacity of the testing machine.
Regards,
Thomas Cuff
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1- Please describe a 5-color flow cytometry panel (specific colors) with a death dye that requires NO/or minimum compensation (The flow machine is the LSR for BD).
2- Please describe a flow cytometry typical gating strategy to quantify the protein levels of a protein conjugated with a fluorochrome (for example PE). List what software you typically use.
3- Please elaborate how you typically do immunofluorescence analysis (level of complexity and depth of analysis). This can be very time consuming and complex.
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Hello Malihe Naderi ! Sure thing, let's get straight to it:
  1. 5-color flow cytometry panel with minimal compensation:Blue 488nm laser: FITC (Green) Yellow-green 561nm laser: PE (Orange) Red 640nm laser: APC (Far Red) Violet 405nm laser: Pacific Blue (Blue) Violet 405nm laser: Live/Dead stain like the amCyan or Aqua (specific colors often for dead cells) The idea here is to choose fluorochromes that have distinct emission spectra to reduce spectral overlap, hence reducing the need for compensation.
  2. Gating strategy to quantify protein levels conjugated with PE:Step 1: Forward Scatter (FSC) vs. Side Scatter (SSC) to gate on overall cells and exclude debris. Step 2: Apply a gate on Live/Dead staining (if used) to exclude dead cells. Step 3: FSC-Height vs. FSC-Area to exclude cell aggregates or doublets. Step 4: PE histogram or PE vs. another parameter (if dual staining). This will allow you to identify the intensity of PE signal which correlates with protein levels. Software: FlowJo is a common choice for analyzing flow cytometry data.
  3. Immunofluorescence analysis:Preparation: Start with fixation, often with paraformaldehyde, and then permeabilize cells (commonly with Triton X-100). Block non-specific binding sites (usually with a serum). Staining: Incubate your cells with primary antibody against your target protein, followed by a fluorochrome-conjugated secondary antibody. DAPI can be used to stain nuclei. Imaging: Using a fluorescence microscope, capture images ensuring you don't have any bleed-through between channels. Analysis: Software such as ImageJ (free) or FIJI can be used. Measure fluorescence intensity, co-localization, or count positive cells. Complexity: The depth of the analysis depends on the question at hand. If you're quantifying fluorescence intensity, make sure to subtract the background. If analyzing co-localization, consider using plugins like JACoP in ImageJ. Remember, while the basics are covered here, the devil's in the details. Always optimize and validate your experimental setup!
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  • I am converting an IPM configuration with random winding to hairpin winding using the same rotor profile and same number of turns, by optimizing stator slot dimensions, by giving the same input voltage,
  • However, I am observing change in back emf value between two configurations at same magnet temperature.
  • What is the reason behind this?
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Thanks for your response
Leo Devasagayam
. SPP is kept the same for both configurations. However slot shape is changed to parallel as for hairpin
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How can machine and deep learning techniques be adapted or fine-tuned to accommodate variations in brain tumor types, locations, and patient populations for more personalized diagnosis and treatment?
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YES!! Deep learning techniques can indeed be adapted and fine-tuned to accommodate variations in brain tumor types, locations and patient populations. Deep learning models are known for their ability to learn intricate patterns and features from complex data, and this adaptability makes them promising tools for medical image analysis including brain tumour detection and classification.
Here are some tips on how this adaptations and fine – tuning can be achieved:
1. Data Collection and Annotation: gathering a diverse and representative dataset is crucial. This dataset should encompass various brain tumour types, different locations within the brain, and a range of patient demographics. The dataset should be properly labeled with accurate annotations indicating tumour type, location, and other relevant information.
2. Preprocessing: before feeding the data into a deep learning model, preprocessing steps are necessary. The steps might involve resizing the images, normalizing intensities, removing artifacts, and more, to ensure consistent and high quality input.
3. Architecture Selection: choosing an appropriate deep learning architecture is essential. Convolutional Neural Networks (CNNs) are commonly used for medical image analysis. However, more advanced architectures like 3D CNNs,
Attention mechanisms and even hybrid architectures can be explored for the better accuracy and adaptability.
4. Transfer Learning: transfer learning involves using a pre – trained deep learning model as a starting point and fine-tuning it on the specific medical imaging task. This approach is effective as pre – trained deep learning models have learned useful general features from a wide range of data. By fine – tuning, you’re allowing the model to specialize in detecting brain tumours and related features.
5. Data Augmentation: since medical imaging dataset are usually limited in size, data augmentation techniques can be employed to artificially increase the diversity of the dataset. Techniques like rotation, flipping, scaling, and adding noise can help the model become more robust to different variations.
6. Hyperparameter Tuning: the hyperparameters of the deep learning model (learning rate, batch, size, etc) should be carefully tuned to specific tasks and datasets. This can be done through experimentation and optimization techniques.
7. Regularization Techniques: regularization techniques such as drop out, batch normalization, and L2 regularization can help prevent overfitting, and help improve the model’s generalization to new cases.
8. Validation and Evaluation: the model should be thoroughly validated and evaluated on separate test datasets to ensure its performance is consistent and effective for different brain tumour types, locations, and patient populations.
9. Feedback Loop: continuously gathering new data and fine – tuning the data based on real – world feedback from medical professionals can lead to further improvements in its adaptability and accuracy.
In summary, deep learning techniques can be tailored to address the specific challenges posed by variations in brain tumour types, locations and patient populations. The success of such adaptations depends on the availability of high – quality data, thoughtful architecture choices, careful preprocessing, and iterative refinement through fine – tuning and validation.
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What are the ethical and regulatory considerations associated with the integration of machine and deep learning technologies in brain tumor identification, and how can patient privacy and data security be ensured?
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The integration of machine and deep learning technologies in brain tumor identification brings to the forefront critical ethical and regulatory considerations. As these technologies offer promising advancements in accuracy and efficiency, concerns emerge regarding patient privacy, informed consent, and the potential impact of algorithmic biases. Striking a balance between the benefits of these innovations and safeguarding patient rights requires robust regulatory frameworks that govern data usage, sharing, and patient confidentiality. Collaboration among medical experts, technologists, ethicists, and policymakers becomes essential to ensure the responsible and transparent deployment of these technologies, aligning medical progress with ethical standards and regulatory compliance.
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I am final year student. I want to start my research work with machine learning. So I am now overwhelmed that what area should I take as a beginner. Please tell me some area as well some topics for that.
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Emerging research areas in machine learning encompass federated learning, quantum machine learning, explainable AI, and AI for healthcare. These fields promise transformative impacts on technology, society, and industry, shaping the future of intelligent systems and fostering ethical, responsible AI advancements.
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How can transfer learning and data augmentation techniques be leveraged to overcome data scarcity and improve the generalizability of machine and deep learning models for brain tumor analysis?
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Transfer learning employs pre-trained models on abundant data to enhance performance on smaller datasets. Data augmentation involves creating variations of limited data. Combining these techniques, pre-trained models extract useful features, while augmentation enhances dataset diversity, mitigating data scarcity and boosting model generalization for improved outcomes.
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What are the state-of-the-art machine and deep learning techniques used for brain tumor identification, and how do they compare in terms of accuracy and efficiency?
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AI-based methods, specifically deep learning algorithms, have shown great promise in brain tumor identification and segmentation from medical imaging data. Here are some of the state-of-the-art techniques used:
  1. Convolutional Neural Networks (CNNs): CNNs have been widely used for image classification tasks, including brain tumor identification. They can automatically learn features from raw pixel data, eliminating the need for manual feature extraction. One popular type of CNN used in medical imaging is U-Net, designed specifically for biomedical image segmentation.
  2. 3D Convolutional Neural Networks (3D-CNNs): These networks process data in three dimensions, making them useful for brain tumor identification in 3D imaging data, such as MRI scans.
  3. Recurrent Neural Networks (RNNs): RNNs are used in sequential data and can be applied to medical imaging by considering each slice of an image as a sequence. This approach can capture spatial dependencies in 3D imaging data.
  4. Transfer Learning: Given the limited availability of labeled medical imaging data, transfer learning is often used in this field. Pretrained models (usually trained on large-scale image datasets like ImageNet) are fine-tuned on the specific task of brain tumor identification, which can improve performance and reduce training time.
  5. Ensemble Learning: Ensemble learning methods combine several machine learning models to achieve better performance. This approach can also be applied in brain tumor identification to combine predictions from multiple models.
  6. AutoML (Automated Machine Learning) Techniques: These are being used increasingly to automate parts of the machine learning process, including hyperparameter tuning, model selection, and feature selection.
In terms of accuracy, deep learning methods (especially CNNs and their variants) have achieved state-of-the-art results on several brain tumor imaging datasets. For example, on the BraTS (Multimodal Brain Tumor Segmentation Challenge) dataset, deep learning methods consistently rank at the top.
However, these methods can be computationally expensive and often require large amounts of data to achieve high performance. Also, while they can achieve high accuracy, they can also be "black boxes," making their predictions difficult to interpret, which is a significant challenge in healthcare where interpretability is crucial.
Therefore, while deep learning methods are the most accurate for brain tumor identification, other factors, such as computational efficiency, data availability, and interpretability, also need to be considered when choosing a method. It's also worth mentioning that ongoing research continues to improve upon these techniques and develop new methods that balance accuracy, efficiency, and interpretability.
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The ultimate goal of AI is to develop machines that can replicate or surpass human intelligence, leading to advancements in technology, automation, and improvements in various fields of human endeavor. However, AI also raises ethical considerations, including issues related to job displacement, privacy, bias, and the potential for misuse.
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There are several ways in which we can ensure the responsible use of artificial intelligence and prevent potential negative consequences:
1. Regulations and Policy: Governments and international bodies should actively work on establishing regulations for AI use. Policies can set standards for privacy, security, transparency, and accountability. They should also outline potential penalties for misuse or violation of these standards. Moreover, policy-making should be an inclusive process, with input from diverse stakeholders, including ethicists, AI researchers, the public, and representatives of groups that could be disproportionately impacted by AI.
2. AI Ethics Guidelines: Many companies and research organizations are developing AI ethics guidelines. These guidelines help define how AI should be developed and used in a way that upholds ethical standards. This includes principles such as transparency (being clear about how and why AI systems make certain decisions), fairness (avoiding bias in decision-making), and accountability (holding developers and users responsible for how AI is used).
3. Transparency and Explainability: AI systems should be designed to be transparent and explainable. This means users should be able to understand how the AI system makes decisions and predictions. Transparency and explainability can be promoted through methods such as open-source AI, which allows for public scrutiny of AI systems.
4. Audits: Regular audits of AI systems can help identify and address issues related to bias, discrimination, or other negative impacts. These audits should be performed by independent third parties to ensure objectivity.
5. Education and Training: AI literacy and education should be promoted at all levels of society. Understanding the capabilities and limitations of AI can help people make informed decisions about its use. In addition, AI developers should receive training in ethics and the potential societal impacts of AI.
6. Privacy Protections: Robust privacy protections should be built into AI systems. This includes anonymizing data where possible, being clear about what data the AI system collects and how it is used, and allowing users to opt out of data collection.
7. Inclusion: AI development should be an inclusive process, incorporating diverse perspectives. This can help ensure that the needs and concerns of all users are taken into account and can help avoid bias in AI systems.
In conclusion, ensuring the responsible use of AI is a complex and ongoing challenge that requires action from various sectors of society, including government, industry, academia, and civil society.
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I have seen once a video of a machine for planting Kappaphycus using tie tie. I would like to recover the video and contact people who made it.
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the "tie-tie method" for the mechanization of Kappaphycus (a genus of red algae commonly known as cottonii and seaweed) is not a widely known or established term in the scientific literature or aquaculture community. It is possible that the term or method may have emerged or gained recognition after my knowledge cutoff date.
The cultivation of Kappaphycus seaweed typically involves the process of "farming" or "mariculture." The standard practices for Kappaphycus farming include the use of floating rafts or lines in the sea where the seaweed is attached to these structures for growth and harvesting.
If the tie-tie method has been developed or utilized more recently, it may involve a specific technique or variation in the way Kappaphycus is cultivated or mechanized. To find the most up-to-date and accurate information on this topic, I recommend conducting a search in academic journals, aquaculture publications, and other reputable sources for any new developments or practices related to the mechanization of Kappaphycus using the tie-tie method. Additionally, reaching out to experts or researchers in the field of seaweed aquaculture could provide valuable insights into this specific method.
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I am working to check the accuracy between Ultrasound Machine and Pathology Lab results for Kidney disease.
Which statistical test to use for comparison of these two independent variables ?
Topic is: Accuracy of Ultrasound Echogenicity with Serum Creatinine in Renal Parenchymal Disease.
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If the experimental design will be recording a significant amount of false-negative and false-positive observations, then the ROC will have a big advantage over the student t-test.
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I used a semi automatic capsule filling machine to filled the 300 mg capsules and there was about 1 capsules which had percentage deviation more than 7.5 following the BP 2013. What are the causes of a problem?
Thanks in advance
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A high percentage deviation for capsules, also known as weight variation or content uniformity, can be caused by various factors related to the manufacturing process or the quality control of the capsules. Here are some possible causes:
  1. Raw Material Variability: Inconsistent or poorly controlled raw materials, such as active pharmaceutical ingredients (APIs) or excipients, can lead to variations in the weight of the filled capsules.
  2. Mixing Issues: Inadequate or improper mixing of the capsule contents can result in uneven distribution of the API and excipients, leading to weight variations among capsules.
  3. Capsule Filling Machine Calibration: Improper calibration of the capsule filling machine can cause inaccurate dosing of the capsule contents, resulting in weight deviations.
  4. Machine Malfunction: Mechanical issues with the capsule filling machine, such as uneven dosing mechanisms or clogged parts, can contribute to weight discrepancies.
  5. Capsule Shell Variability: Variations in the quality or size of the capsule shells can affect the final weight of the filled capsules.
  6. Environmental Factors: Changes in humidity and temperature during the manufacturing process can influence the flow properties of the capsule contents, leading to inconsistent filling.
  7. Human Error: Manual handling of capsules or errors during the filling process can cause weight variations.
  8. Inadequate Quality Control: Insufficient or ineffective quality control measures during production may fail to identify weight variations in capsules.
  9. Improper Storage: Improper storage of filled capsules after production can lead to changes in their weight due to moisture absorption or evaporation.
  10. Process Variability: Lack of process standardization or deviations from standard operating procedures can contribute to weight discrepancies.
  11. Quality of Tamping: In hard gelatin capsule manufacturing, improper tamping can cause uneven compaction of the capsule contents, leading to weight variations.
  12. Capsule Size Variation: If different capsule sizes are used during manufacturing, this can impact the weight deviation of the filled capsules.
To address high percentage deviation for capsules, manufacturers should implement rigorous quality control procedures, maintain consistent raw material sourcing, regularly calibrate equipment, and ensure proper training of personnel involved in the manufacturing process. Regular monitoring and adjustments to the production process can also help to minimize weight variations and ensure the content uniformity of capsules.
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I am looking to characterize a contrast agent I'm developing for relaxivity. At my university, I have access to a Esaote Vet-MR Grande. Is it possible to get relaxation time measurements from this machine or do you need a machine that is specialized for quantified MRI? If it is possible, how? I've found various protocols giving parameters for machine settings but we are new to this and need help starting at the very beginning if it is possible. Thanks!
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Even without any programming you can get T1 measurements using saturation recovery. This is the LEAST effective method but it can be done even if your system doesnt have a inversion recover sequence.
Using a Gradient echo sequence - you increment TR in a simple series of scans. You will need to turn off Auto leveling in your out put and manually set your receiver gain but this can be done. Then you acquire a number of scans with TR incremented in like something like a power of 2 series
(10ms, 20ms, 40ms, 80ms, 160ms, 320ms, etc). You can either perform the log-lin fits to get the T1 or use the plugin that is available for ImageJ.
You probably have a spin-echo sequence in your system. Use a long TR (after you determine it above). And increment a series of scans in TE similarly described. It won't be as accurate as a multi-echo technique but better then none. Again you can do the fits yourself or ImageJ.
No autoscaling. Must be absolute value. And this will work for the complex modulus images your scanner will produce..
Hope that helps.
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Material: Fiberglass (GFRP) Thickness: 3mm
Machines: Laser - Wire Cut - CNC Router - CNC Milling - Jigsaw
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The best cutting machine for cutting cylinder-shaped objects made of Fiberglass (GFRP) depends on various factors such as the specific requirements of your project, the size and thickness of the cylinders, and your budget. Each of the machines you listed has its own advantages and limitations when it comes to cutting fiberglass materials. Let's go through each one:
  1. Laser Cutting Machine: Laser cutting is precise and offers excellent cutting quality. It is well-suited for intricate shapes and can handle thin to medium thickness fiberglass materials. However, it might not be the most efficient option for cutting thick cylinders due to the melting and slow cutting speed associated with thicker materials.
  2. Wire Cut EDM (Electrical Discharge Machining): Wire EDM is best suited for cutting complex shapes with high precision. It can be effective for cutting fiberglass cylinders, but it may not be the most cost-effective option for larger and thicker cylinders.
  3. CNC Router: A CNC router is a versatile machine that can handle various materials, including fiberglass. It is excellent for cutting larger cylinders with moderate precision. It might not be the best option for extremely intricate shapes, but it's suitable for many applications.
  4. CNC Milling Machine: CNC milling can be used for cutting fiberglass, but it's better suited for flat or 3-axis milling applications. While it can create cylindrical shapes, it may not be as efficient as other specialized machines for this specific task.
  5. Jigsaw: A jigsaw is a handheld cutting tool and might not be suitable for precise and consistent cutting of fiberglass cylinders, especially if you require high accuracy and smooth edges. It's more suitable for simple DIY projects and not recommended for industrial-scale operations.
Given the material (Fiberglass - GFRP) and the requirement for cutting cylindrical shapes, I would recommend considering a CNC Router. CNC Routers offer a good balance between precision, versatility, and cost-effectiveness for cutting cylinders made of fiberglass. They can handle thicker materials and create accurate cylindrical shapes efficiently.
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By adding a tungsten electrode and adding a gas hoseBy adding a tungsten electrode and adding a gas hose
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Your response, "Better do not :) But all is possible if you want to spend a lot of cash," is somewhat in line with the practical considerations I mentioned in my previous answer. While it may be technically possible to convert an arc welding machine into a TIG welding machine with the addition of inert gas, it would indeed require significant modifications and expenses. Here's a justification for the Janusz Rebis response:
1. Cost of Modifications: Converting an arc welding machine into a TIG welding machine would involve replacing or modifying the power supply to provide a constant voltage output. This could require rewiring and purchasing additional components, which can be expensive. Furthermore, the necessary changes to the control circuitry, gas flow system, electrode configuration, and other components would also contribute to the overall cost.
2. Expertise and Labor: Converting an arc welding machine into a TIG welding machine is a complex task that requires expertise in electrical engineering, welding processes, and control systems. It would likely require the involvement of skilled professionals to ensure the modifications are done correctly and safely. The cost of their labor would further add to the overall expenses.
3. Reliability and Performance: Converting a welding machine from one process to another may compromise the reliability and performance of the equipment. Arc welding machines are specifically designed and optimized for arc welding processes, while TIG welding machines are tailored for TIG welding requirements. Modifying an arc welding machine to perform TIG welding may result in suboptimal performance, reduced efficiency, and potential issues with weld quality and consistency.
4. Availability of Dedicated Equipment: Dedicated TIG welding machines are readily available on the market and are designed specifically for TIG welding applications. These machines come with the necessary features, controls, and capabilities to ensure efficient and reliable TIG welding. Investing in a purpose-built TIG welding machine would likely provide better results, increased productivity, and long-term cost-effectiveness compared to attempting to convert an arc welding machine.
In summary, while it might be technically feasible to convert an arc welding machine into a TIG welding machine with the addition of inert gas, the associated costs, expertise, potential reliability issues, and the availability of purpose-built TIG welding machines make it more practical to invest in dedicated equipment.
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When we used the pen, the books we touched, the sheets, the notebooks, everything had a life, now everything is machine and robots, our brains are in danger of being altered !
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Every era we adapt ourself gradually in all aspects of life among these teaching using chalk ,board so ...on and online teaching notebooks
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One Thing, Your Physics Book Many Equations Depend On Uniform Velocity And Acceleration Equation But Nothing Is Uniform All Time And Change Should Be And Must Be Come Every Where In Universe About Velocity And AccelerationAt Physics Books Those All Uniform Velocity And Acceleration Can Be More Or Less Correct For All Uniform Velocity And Acceleration World But Not For Practical Life Equation Cause Nothing Is All Time Uniform In This Life And In Heaven Also.When Moment Change And Time Change And When There Are Day,Night,Morning,Noon,Afternoon,Evening,Night That Moment Change Sky,Cloud,River,Pond,Mountain,Rain,Storm,Breeze,Drizling,Cats And Dogs And Others Then Also Velocity And Acceleration Of Life And Planet Change And When Mass Increase.Without There Would Not And Will Not Life Beauty.Life Would Be And Will All Time Alike And All Time Uniform And No Taste And Color Of Life.Kids Would Be Forever Kids,Parents Would Be Forever Parents. Universe.Its Research And Scientists Say Planets Movement And Rolling Never Follow Isac Newton Equation And Isac Newton Rule
Newton”s First Law:No Outside Force Motionless Elements Forever Motionless But Motion Elements All Time Motion.
Ans:Wrong Because No Outside Force Elements Has Inside Force.And Others Wise Actually Elements Are Not Only Electron,Proton,Neutron And Every Elements Has Different Characteristic And That’s Why Chemical Characteristics Different And That’s Why Their Strength And Characteristics Different And That’s Why Elements Not Only Electron,Proton,Neutron And There Are Many Atom Just Like Electron,Proton,Neutron That’s Why Characteristics Different And That’s Why Different Different Elements.There Are Many Atom(More Than 150 Atom Inside Every Chemistry Elements And Its Atom Number Is Vary Elements To Elements-If We Are See Chemistry Nucleaus And Chemistry(Organic Or Inorganic) Elements Or Reaction Under Plasma Microscope Or Satellite Frequency Microscope Or Very Strong Microscope Than We Will Be See Totally Different World Of Chemistry Which Is More Or Less Totally Different From Our Chemistry Book And Also Never Ever Only Chain Reaction Happens In Organic Chemistry.And Chemistry Nucleas Is That Which Secret Frequency And Secret Vein Just Like Leaf To Compact Others All Atom And Under Plasma Microscope Or Satellite Frequency Microscope We Will Be Able To See Accurately Nucleus Which Secret Frequency And Also Vein Just Like Leaf To Compact All Atoms.Nuclues Is Never Proton And Neutron…..If Nucleaus Is Only Proton And Neutron Than When Environment Partial Reaction Will Be Happen And Temperature,Air,Light,Color And Environment Different And Fraction Will Be Come Than When Proton Will Be Go Away And All Over Atom Distribution Will Be Broken And All Will Be Broken.So,There Are Many Atom Inside Elements. . Chemistry Basic Atom Not Only Electron,Protron Or Neutron And There Are Others Basic Atom Within Elements And That’s Why Characteristic Different And Vary Places To Places.Changeno Atom,Airono,Waterono,Cloudono,Massono,Environmentallono,Specifino,Tastetono,Reactono And Others Many Atom(Just Like+_*%#!) Within Elements And It Is Vary Environment To Environment And Places To Places Or Planet To Planet.Atom Distribution Equation-----q*v*theta(sin,cos,tan or others)/Time Or Changing Time----Here---q=Atom Charge---Velocity----Theta---Atom Position With TimeIf We Are See Chemistry Nucleaus And Chemistry(Organic Or Inorganic) Elements Or Reaction Under Plasma Microscope Or Satellite Frequency Microscope Than We Will Be See Totally Different World Of Chemistry Which Is More Or Less Totally Different From Our Chemistry Book.And Chemistry Nucleus Is That Which Secret Frequency And Secret Vein Just Like Leaf To Compact Others All Atom And Under Plasma Microscope Or Satellite Frequency Microscope We Will Be Able To See Accurately Nucleus Which Secret Frequency And Also Vein Just Like Leaf To Compact All Atoms
Now Without Outside Force Motionless Elements Never Forever Motionless Or Motion Elements Never Forever Motion Because They Have Specific Characteristics And Inside Temperature, Pressure And Atom Elements Just Like Electron,Proton,Neutron And They Will Do Reaction And Others Velocity And They Have Half Yearly Age Because Every Elements Should Be Do Reaction And Die Or Convert Or Change Because Planet Mass Increase Everytime And When Only If Single Something Change Than Change Everything.So,Aisac Newton Equation Should Be Wrong.Aisac Newton Equation Can Be True That Time When There Would Be No Constellation Or Universe Because Change Should Be Come Today Or Tomorrow And Every Time Because Nothing Is Uniform Velocity And Acceleration Here And In Heaven Life Forever.
Solve Equation:No Outside Force Motion Elements Can Be Motion But Once Inside Electron,Proton,Neutron And For Others Basic Atom Like Airono,Pressurono,Timeno,Frequencyiano,Reactionon,Relationono,Rationono,Waterono,Environmentolono And For Others Basic Atom Motion Elements Can Be Do Reaction And Once Motionless And It Can Be Slight Motion Increases But Once Motionless Cause There Are Many Many Basic Atom In Environmental Elements And Their Ratio And Velocity Different And That’s Why Characteristics Different And Sometimes Vary Place To Place Or Place And Distance Change And They Have Half Yearly Age And Environment Has Recycling Process And Partial Reaction And Its Gonna Convert Others Like Dhancha Plant When Die Then Convert As Green Fertilizer.And Same Words For Motionless Elements.And Motion Elements Never Wanna Forever Motion And Motionless Elements Never Wanna Forever Motionless Cause It Has Utter Energy And Basic Atom Reaction And Velocity And Ratio And Environmental Partial Reaction And Recycling Process For Life.
Now,Suppose Anything Is Motion And No Outside Force:Motion Elements=Total Unit( Time And Others)*Summation Of Velocity*Inside Utter Energy Change*(Like Basic Atom Ratio And Velocity Change And Environmental Partial Reaction And Recycling Process Change)=Last Step Can Be Motionless Or Sometimes Slight Motion Increases And Once Inert Elements And Scattered………… And Here Elements Came From Environment.And Motion Less Elements Will Be Slight Motion And Once Scattered And Equation Motionless Elements=Total Unit( Time And Others)*Summation Of Slight Increases Velocity*Inside Utter Energy Change*(Like Basic Atom Ratio And Velocity Change And Environmental Recycling Process Change))=Last Step Can Be Motionless Or Sometimes Slight Motion Increases And Once Inert Elements And Scattered.
Newton 2ndLaw:Force Proportional Momentum Change(Wrong)
Ans:When We Give Force On Elements It Can Be But Elements Has Also Own Force And Momentum.Example:Suppose Two Things Running:
M1=2, M2=50
V1=3,V2=80
K1=3,K2=80
So,It Should Be After Collusion Small Things Velocity Must Be Highly Increase And Big Things Velocity Also Increase And It Depends On Two Elements And Environment.
Solve:Force And Momentum Change Depends On Elements.Suppose One Ball When You Will Be Kick Then It Will Get Easily More Velocity But When You Will Convert Same Ball To Any Sheet And Give Same Force Then Its Momentum Change And Both Momentum Change Should Not Be Same.And Force And Momentum Change Depends On Elements And Size And Environment Also.Suppose You Are Wanna To Fall One Thing From Mountain Then Just Touch And It Will Be Get Huge Force And Velocity But Your Force Was Very Slight And If You Will Give Same Same Force On Normal Environment Then It Will Not Get Same Velocity And Force.So,Its Depend On Environment And Environmental Recycling Process.
Equation:F1=M1*Dx1/t1 And F2=Dx2/t2 Now After Accident F1*F2=M1*Dx1/t1*(Momentum Change That Distance And Time That Velocity With Time Change Unit With Environmental Change)*M2*Dx2/t2
Now F1**(Momentum Change That Distance And Time That Velocity With Time Change Unit With Environmental Change)=/<_(Not Equal)>_(Not Equal)F2*(Momentum Change That Distance And Time That Velocity With Time Change Unit With Environmental Change)
Newton 3rdLaw:Every Force Has Equal And Opposite Force(Wrong And It Can Be True For Slight Time But Not All Time) Ans:When We Give Force On Elements It Can Be But Elements Has Also Own Force And Momentum.Example:Suppose You Are On Mountain And Just Touch A Big Stone By Finger Which Will Be Go To Touch Soil And Get Huge Force When Newton Under Apple Tree And Break Newton Head.So,What Will Be Opposite Force Of Newton Broken Head.Or You Are Pushing A Pin At Wall By Hammer…Pin Is Going To Wall But Hammer Does Not Get Same Opposite Force.Suppose Two Things Running:
M1=2, M2=50
V1=3,V2=80
K1=3,K2=80
So,It Should Be After Collusion Small Things Velocity Must Be Highly Increase And Big Things Velocity Also Increase And It Depends On Two Elements And Environment.So,Elements Force Should Not Be Equal And Opposite. You Are Giving A Kick To A Truck And Truck Has No Reaction Force But Your Leg Is Broken.Truck Not Give Same And Equal Force.Newton Gave Bullet And Gun Equilibrium Force Equation But Now Many Bullet Donot Give Opposite Force After Release.And Same Equation For Boat Also.And I Am Giving Something Fall From Moutain Or Foorball Or Truck Velocity And Acceleration Equation.
So,It Should Be After Collusion Small Things Velocity Must Be Highly Increase And Big Things Velocity Also Increase And It Depends On Two Elements And Environment.So,Elements Force Should Not Be Equal And Opposite.
Equation:F1=M1*Dx1/t1 And F2=Dx2/t2 Now After Accident F1*F2=M1*Dx1/t1*(Momentum Change That Distance And Time That Velocity With Time Change Unit With Environmental Change)*M2*Dx2/t2
Now F1**(Momentum Change That Distance And Time That Velocity With Time Change Unit With Environmental Change)=/<_(Not Equal)>_(Not Equal)F2*(Momentum Change That Distance And Time That Velocity With Time Change Unit With Environmental Change)
Newton Gave Bullet And Gun Equilibrium Force Equation But Now Many Bullet Donot Give Opposite Force After Release.And Same Equation For Boat Also.And I Am Giving Something Fall From Moutain Or Foorball Or Truck Velocity And Acceleration Equation.
And For That Motion Of Rocket Equation Was Wrong Because It Was Depend On Newton”s 3rdLaw: When You Will Be Go From Soil To High Sky Than Gravitational Attraction Increase That Velocity Decrease But Once Near Unventilated Places Gravitational Attraction Decrease And Rocket Velocity Increase And Plane And Rocket Different Things But Alike.And Free Velocity Should Not Be All Time 9.8 ms-2.And It Should Be Different Elements To Elements Either Up And Down.So,When You Are To Go Up Than Every Second Before Reached Unventilated Place Velocity Should Be Decrease For Gravitational Attraction.
Motion Of Rocket:
Rocket Mass:M
Gas Mass: Δm (Delta Mass) In Every Seconds
One Second Gass Mass = Δm
Δt (Delta Time) Gass Mass= Δm (Delta Mass)/ Δt (Delta Time)
Now Force F=Ma
HERE, M=Rocket Mass
a=v/t,
Δm (Delta Mass)/ Δt (Delta Time)*t
.
Force=M(Rocket Mass)* Δm (Delta Mass)*Increase Gravitational Attraction That Deacrease Rocket Velocity With Environmental Temperature And Pressure And Others And Increase Velocity By Force With Environmental Temperature And Pressure/ Δt (Delta Time)
So,HereGass Mass Should Be Higher Than Or Bigger Than Rocket Mass And Everything Seconds It Will Change For According To Environment.So,Newton 3rd Law Should Not Be Work Here Beccause It You Are Use Newton 3rd Law Than Rocket Shuttle Should Be Broken For Environmental Pressue And Temperature And Rocket Should Be Fall From Sky.
Now Neednot And Shouldnot Use Rocket.Now You Can Use My Triangle Vehicle Which Will Be Go Electric Recycling.IDonotKnow,You Will Be Albe Or Not My Triangle Vehicle Cause It Has Very Sharp Design.You Can Try But May Be You Cannot Make My Triangle Vehicle Which Will Fly In The Sky,Run On Road,Swim On Water And Dive Under Water.And.You Can Try But It Has Very Sharp Design
Now………1.Anything Is Running That Motion And Last Point Reached Equation:
Let,Suppose One Thing Is Running On V Velocity
After One Second(1s) It Will Be Go=V*1
Now T Second It Will Be Go=V*T But Now What Will Be Its Velocity Change And Equation:
In One Second=V*1 That Dx1/t1 Now 2 Second It Will Be Dx2/t2 And 3 Second It Will Be Dx3/3 And 4 Second It Will Be Dx4/4.Now Dx Can Be Change From 1 Second Or 2 Second Or 3 Second Or 4 Second.Now What Will Be Motion Elements Reached Point Equation After Time:
It Will Be Dx1/t1+Dx2/2+Dx3/3+Dx4/4 That 4Seconds*Summation Mean Of Velocity Change Or Velocity Summation (Dx1/t1+Dx2/2+Dx3/3+Dx4/4) That 4*Summation Mean Of Velocity Change And Others All Plus In 4 Seconds.
That((Dx1/t1+Dx2/2+Dx3/3+Dx4/4).
So,Specific Point Reached Equation After Time And Velocity Change Will Be
Specific Point Reached=4*Summation Of Mean Of Velocity And Time Change That Distance And Time Change And Others All Plus In 4 Seconds.
Specific Point Reached=Total Unit(Time And Others)*Summation Of Velocity
And Specific Point Reached Mean Velocity=Total Unit(Time And Others)*Summation Of Acceleration(Acceleration Mean Change Of Velocity That Distance And Time Change)
So,All Time Changing Velocity(Not Uniform) And Acceleration Equation Is:
V1+V2+V3+V4+V5 And a1+a2+a3+a4+a5
SPR=Total Unit Or Total Time*Mean Summation Of Velocity Or Acceleration.
Now Last Velocity When Velocity Change All Time More Or Less.So Last Velocity And First Velocity(Not All Time Uniform):
SPR=V1+3*Mean Summation Of Three Velocity+V5
Now,S-3*Mean Summation Of Three Velocity=V1+V5
S-F(F3MSTV)=V1+V5
Now v5=E-V1…….Here (S-F=E)
Motion Of Falling Elements:
1stVelocity=0 But When Fall From Upper Sky Velocity Low But When Fall From Near Soil Velocity High For Attraction Cause(Lower Portion Gravitational Attraction Is High).
Suppose Falling Fruit From Ifel Tower Head And Every Meter Per Second ms-1 Velocity Increases Not All Time Alike 9.8 Ms-2. Cause Its Also Depends On Environment And Elements.Its Also Not Possible For All Uniform Equation Cause Elements To Elements 9.8 Vary.
Here Suppose Vo=0 Now Vo+V1*1+V2*2+V3*3(Here Velocity Increases With Fall Attraction)
Now Last Velocity Will Be=Vo+Increases Attraction*Summation Of Mean Velocity
Suppose Increasing Attraction Velocity=g
So,Last Velocity Will Be=Increases Falling Attraction*Summation Mean Of Velocity*Total Time+Vo
So,Last Velocity Will Be=Mean Increases Falling Attraction Velocity*Summation Of Mean Velocity*Total Time+Vo (Some Error Can Be Come But Error Should Be Identify)
And So,After Soil Touch Velocity Equation Will Be=(V-Last Velocity Increases Attraction After Touch)=Increases Mean Falling Attraction Velocity*Summation Of Mean Velocity*Total Time+Vo
(If Need You Can V-LVIAAT Or V+LVIAAT)After Touch AsNecessity.Here Vo=0 Others Can Be
Now Last Velocity And Distance Equation Will Be That After Soil Touch Falling Elements Equation Will Be=Vo+Summation Of Mean Velocity*Mean Increases Falling Attraction Velocity*Total Time+Velocity-Last Velocity Increases Attraction*1unit
From Soil Low To High:VelocityDesreases With Gravitational Attraction But Once Near Two Point Of Planets That Near Unventilated Places Velocity Increases
That SPR=Vo+Summation Of Mean Velocity*Total Time Unit*Decreases Attraction Velocity+(V+Last Velocity Decreases)*I Unit.
Laws Of Static Friction:
1.Motionless Varnish React Inverse Of Elements Motion
Ans:It Can Be True But Not All Time.Suppose One Boat On River.And Boat Is Motionless But River Water Wave Velocity Increases For Air Environment.And Environment Has Changing And Recycling Process.So,Boat And Water Varnish Both Velocity Also Increases.So,Equation Is Going To Be Wrong.Now It Can Be Sometimes True Or Many Times Also Like Cycling On Road Or It Can Also True Motion Increases But Mass Huge And That’s Why Gonna To Be Slow Or Stop.
Equation:Motionles*Varnish Force*Last Velocity Will Be=(V-Last Velocity Increases Or Decreases Attraction)*Increases Or Decreasing Attraction*Summation Mean Of Velocity*Total Time+Vo
=(V-Last Velocity Increases Or Decreases Attraction)*Increases Or Decreases Mean Attraction Velocity*Summation Of Mean Velocity*Total Time+Vo …..Here Vo Can Be=0 Or Others
Equation2:Motionles*Varnish Force Proportional To Stop Or Obstruct Force
Ans:How It Can Be True Cause Water And Boat And Mountain Or Truck Or Cycle Or Football Example.Cause Sometimes Can Be Increases Or Decreases
Equation Just Like 1st And S1=U1VI And S2=U2V2 And So,Here Not Proportional.
Equation3:Angel Of Repose Proportional To Last Border Varnish
Answer:Suppose One Boat On Rivet Or One Oil Machine Machine By Cow.If You Will Be Give Slight Force On Boat Border Than Its Move More Cause Lower Touching Portion Varnish Is Soft And It It On Soil Or Muddy Then It Would Be Give More Force To Move.Suppose Football Player Corner Kick,ItsGonna Here And There And Many Times Not On Specific Cause Environmental Cause Air,Temperatire,Pressure And Own Utter Energy Cause.So,Its Depend On Environment And Utter Energy Of Both Elements.
Equation Like Before And You Can Use My New Mathmatics Equation But It Can Be Increases And Decreases As Necessity And Length And Angel Can Increases And Decreases And But It Will Be Very Helpful For Cow,Goat,Horse That Animal Organ Convert For People Like Bones,Eyes If You Are Modify And Change Them 2 Or 3 Places Or More As Organ Then You That People Can Use Those Normaly But Need Plant And Plant Enzyme And Others Enzyme And Color Convert Also.
Equation4:Varnish Mean Never Depends On Touching Places And Volume
Answer:Its Ultimately Wrong If You Read My Previous Upper And Others Equation.
Equation5:Varnish Mean Never Depends On Area
Answer:UltimatelyWrong.Cause One Big Thing And One Small Thing Varnish Should Not Be Same And Also Depends On Both Area And Environment Also Like Water,Desert,Normal,Pitch Road Or Normal Village Road And Environment Also.
I Am Giving You Roult Law Example:
When 2 kg Ice+2kg Water Convert To Water Then Its Is 4Kg But According To My Law When 2kg Ice+2Kg Water Convert To Water Then It Can 4.10 Or 3.90 Or 4.20 Kg Cause Environmental Elements Enter Within It.LikeTemperaure,Pressure,Light,Master Force And Others And Why ItsGonna To Be Convert Without Why It Will Be Convert.And When Enter Something Within And React And Then 2+2=4 Kg Should Not Be 4 Kg And It Will Be 4.10 Kg Or 3.90 Kg Or 4.20 Kg Depends On Environment.So,NewRoult Law Will Be According To Me: (n2+n1)/n1=D(P2- Or + P1)/P1
Or (n2+n1/n2)=D(P1- Or + P2)/P2
Or (n1+n2)=D(P1- Or + P2)
Or (n2+n1)=(P2- Or + P1)D………Here P1 And P2 Next Situation Of n1 And n2. D=K And According To My Previous Equation K=Pressure*Temperature/N(Atom)*Volume Or D=K That K=Temperature*Pressure/Volume
Graham Law: Motionless Pressure And Temperature Any Gas Diffusion Per Inverse Density Rot
Answer:Gas Diffusion r=KTPD/Delta Time Here K=Increase Or Decreases With Temperature And Pressure Like Attraction Or Repulsion Equation
MarkonicovLaw:R-CH=CH2+HX …..Here (=)=Two Double Bond Now Solve Equation Will Be R-CH-H-CH2-X It Will Be True Equation Reaction Cause Asymmetrical And Unconnected Or Not Related.
Now You Can Think All About Your Study Equation They Are True Or Not And There Are Fit For Life And Environment Not Cause I Guess They Are Not Fit For Environment And Life Cause All Uniform Velocity And Acceleration Equation And Modified Equation Which Is Not Fit For Life And Forever Cause Here And There And In Constellation Or Universe Nothing Is Uniform Velocity And Acceleration Equation.People,Vehicle And Planet And Constellation And Universe Never Walk Or Run Or Motion Or Motionless As Uniform Velocity And Acceleration Equation.ItsGonna Change When Time Change Or Mass More Or Less Change And Moment Change Like Strom Is Not Uniform Velocity,Tsunami,Rain,MoonLight,Sunlight,Vehicle And Others Nothing Is Uniform Velocity And Acceleration Motion Or Motionless But All Your Study Equation Uniformly Go.I Am Solving According To My Own.ButIts Your Matter Accept Or Not.Now You Can Think Your Own Way And Try To Solve If You Are Guess They Are Wrong.
And Albert Inestine And Salam Glass And Stephen Hocking Equation Wrongly Prove From My Plant Energy,Fragrance,Color And Others Planet Light Absorb Or Mine,Pit,Quarry Find Equation. .............Are Those True About About Uniform Velocity And Acceleration Equation And About Isaac Newton Equations Wrong & Error?.........Please See Attachment For Further Attachment And Discussion.
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I'm wondering if somebody has read this opus from the beginning to the end? I would award Mehadi the Nobel price in literature if he learns that Albert Einstein but not Albert Einestine created the theory of special relativity. Anyway, one more genius in RG
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Hello
How can we determine the maximum rotor current of the double-fed induction generator to protect our machine?
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maximum current is different in lagging or leading load as is different when we want protect our induction generator with two side fed we have to protect in worst situation as lead load and level of sea - temperature - humidity - level of voltage saturation curve rate - internal impedance - and ... is determine and calculate it in maximum current ratio.
in at all best way for calculate maximum current calculate with quantity load connect to generator (ohmic - passive load (lead or lag) ) is determine maximum ratio load .
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I recently obtained a CR2032 coin cell pressing machine manufactured by the GELON lib group for the purpose of building Li-O2 batteries within an MBRAUN glovebox. However, I encountered an issue during the vacuum application in the antechamber, where a significant amount of oil was spilled. To address this problem, I attempted partial vacuum cycles followed by Ar filling within the antechamber. Unfortunately, this approach led to excessive water levels once the machine was inside the glovebox. If anyone has faced a similar challenge, I would greatly appreciate hearing about your experiences and any potential solutions you discovered. Thank you for your assistance.
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I think you may vacuum-seal the machine in a plastic bag, similar to sealing food, and then insert it into the glovebox. There might be a trace of air introduced during this process, but you can do purging or regeneration later. Another way is filling the oil for that machine inside the glove box.
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Hi, in my lab we have an old lightcycler 2.0 qc system that we want to use, unfortunately we do not have the CD, does any one know were can I download the software for this machine?. thanks to everyone in advance
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If you are looking to download the software for the LightCycler 2.0 QC system and you don't have the CD, there are a few options you can consider:
1. Manufacturer's website: Visit the official website of the manufacturer of the LightCycler 2.0 system. They may provide a dedicated software download section or a support page where you can find the software you need. Look for any available updates or downloads specific to your model.
2. Online support forums and communities: Join online forums or communities that focus on molecular biology, PCR, or the LightCycler systems. Engage with fellow researchers who have experience using the LightCycler 2.0 and inquire if they can share the software with you or guide you to a reliable source.
3. Contact the manufacturer directly: Reach out to the manufacturer's customer support or technical support team. Explain your situation and ask if they can provide you with a digital copy of the software or guide you to a legitimate source where you can obtain it.
4. Collaborate with other labs: If you have connections with other research laboratories or academic institutions, inquire if they have the software for the LightCycler 2.0. They might be able to share the software with you or assist you in finding a legitimate source.
Remember, when downloading software, ensure that you are obtaining it from a trusted and authorized source to avoid any potential security risks or infringement of licensing agreements.
I hope you find the software you need for your LightCycler 2.0 QC system. If you have any further questions, feel free to ask. Good luck with your experiments!
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I'm currently doing design of experiments to optimize my hplc method. The 3 response parameters for my design of experiments are Peak retention time, resolution and asymmetry.
For some of my standards, the software automatically calculated the peak resolution and asymmetry but others it did not.
So I need to find a way to get the resolution and asymmetry for the ones not automatically calculated.
Please note, I am using Chromeleon 7 software on my hplc machine
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Damola Ajani To manually calculate peak asymmetry and resolution for a single peak in an HPLC chromatogram using Chromeleon 7 software, you can follow these steps:
1. Identify the peak of interest in your chromatogram.
2. Determine the peak retention time (RT) by locating the apex of the peak. The retention time represents the time it takes for the peak to elute from the column.
3. Measure the peak width at the baseline (Wb) by drawing a tangent line from the baseline to each side of the peak and measuring the distance between these tangents.
4. Measure the peak width at the half-height (Wh) by drawing horizontal lines from the peak apex to intersect with the two sides of the peak. Measure the distance between these intersections.
5. Calculate the peak asymmetry factor (As) using the following formula:
As = (Wh - RT) / (2 * Wb)
The peak asymmetry factor indicates the tailing or fronting of the peak. If As < 1, it indicates tailing, and if As > 1, it indicates fronting.
6. Calculate the peak resolution (Rs) using the following formula:
Rs = 2 * (RT2 - RT1) / (Wb1 + Wb2)
Here, RT1 and RT2 are the retention times of two adjacent peaks, and Wb1 and Wb2 are their respective peak widths at the baseline.
By following these steps, you can manually calculate the peak asymmetry and resolution for a single peak in an HPLC chromatogram. These calculations can provide additional insights into your chromatographic separation and help in optimizing your HPLC method.
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Hello everyone,
What is the most convenient method to machine a notch in a compact tension specimen according to ASTM E647 standard?
I do not have the option to use wire cut EDM and I'm just getting into conducting FCGR.
Thank you
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Hello Shiv Sahaya Shukla , thank you for your suggestion. Unfortunately I do not have a wire EDM facility. Do you have any other, suggestions?
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This is an undergraduate design project, what fields should he really focus on?
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Chemistry, physics, Mechanic, machine in power, economics, tuber crops, soil physics, soil chemistry, irrigation.
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Hello,
I have been trying to search for these machines for 2kw or 2.5kw rating but I couldn’t get a suitable vendor or company In USA. Can anyone please share about purchasing machines ( anyone who is working in wind system research lab who have pmsm pmsg dfig installed). Need information regarding coupling. Please, I need some input.
thank you
Shipra
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We actually have an installed experimental test bench composed of: a permanent magnet synchronous machine, a wound rotor synchronous machine, a squirrel cage induction motor, dSpace 1104, two level three phase converter, variable 600V DC voltage source, three phase current sensor, and a position encoder.
If you need help to conduct an experimental study, we'll be very glad to help you. Contact me in private if you want us to collaborate together.
Have a nice day.
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I am having issues with the lid function on a Biorad CFX-96 qPCR machine.
On powering up the Lid moves to an open position.
The lid will not close, not when I press the button on the front of the machine, and when I select the close lid option in the software, I get an error message:
0000C0069 Lid positioning error. Please power instrument of then back on.
When I turn the machine of and back on it runs basic diagnostics, reporting everything to be OK.
When the power is switched off, I can lower the lid, but it doesn't lock closed, and when the machine is switched back on, the lid moves back to the open position.
Biorad have been informed, but I was hoping someone may have encountered similar issues, or knows of a quick fix, whilst we are waiting for the engineer to pitch up.
Thanks in advance.
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I have the similar issue (lid not closing). Let me know please if any of you could get around this.