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go atlas
mesh space.mult=1.0
#
x.mesh loc=0.00 spac=0.01
x.mesh loc=0.20 spac=0.0001
x.mesh loc=0.25 spac=0.01
x.mesh loc=0.30 spac=0.0001
x.mesh loc=0.40 spac=0.01
x.mesh loc=0.5 spac=0.01
#
y.mesh loc=0.00 spac=0.001
y.mesh loc=0.002 spac=0.001
y.mesh loc=0.005 spac=0.001
y.mesh loc=0.035 spac=0.01
y.mesh loc=0.065 spac=0.15
#
region num=1 material= Air x.min=0 y.min=0
region num=2 material= SiO2 x.min=0.2 x.max=0.3 y.min = 0.002 y.max=0.005
region num=3 material= silicon x.min=0 x.max=0.2 y.min =0.005 y.max=0.035
region num=4 material= silicon x.min=0.2 x.max=0.3 y.min =0.005 y.max=0.035
region num=5 material= silicon x.min=0.3 x.max=0.5 y.min =0.005 y.max=0.035
region num=6 material= silicon x.min=0 x.max=0.5 y.min =0.035 y.max=0.065
#
electrode name= gate x.min=0.2 x.max=0.3 y.min =0.0 y.max=0.002
electrode name= source x.min=0 x.max=0.1 y.min =0.002 y.max=0.005
electrode name= drain x.min=0.4 x.max=0.5 y.min =0.002 y.max=0.005
#
doping uniform concentration= 1E13 p.type region=6
doping uniform concentration= 1E20 n.type region=3
doping uniform concentration=1E13 p.type region=4
doping uniform concentration=1E20 n.type region=5
#
contact name= gate n.poly
inter qf=3e10 y.max=0.005
contact name= source
contact name= drain
#
models cvt srh print
#
#output val.band con.band qfn qfp e.field j.electron j.hole j.conduction j.total ex.field ey.field flowline e.mobility h.mobility qss e.temp h.temp j.disp band.param charge
#
Method gummel newton
Solve init
#Solve prev
#Solve vdrain=0
#Solve vdrain=0.1
#Solve vdrain=0.5
Solve vdrain=1.5
#Solve vdrain=2
#Ramp the gate
#
Log outf=100nm_Vt_output.log master
Solve vgate=0 vstep=0.25 vfinal=3 name=gate
save outf=100nm_Vt_output.str
#plot result
tonyplot 100nm_Vt_output.log
#tonyplot 100nm_Vt_output.str
#extract device parameter
extract name="vt"(xintercept(maxslope(curve(abs(v."gate"),abs(i."drain")))) \
- abs(ave(v."drain"))/2.0)
#
quit
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In this code, there is no direct definition of the threshold voltage (Vt). Therefore, it is not possible to determine why the threshold voltage is negative or positive based on this code alone.
In general, the threshold voltage of a MOSFET can be positive or negative, depending on the type of MOSFET (n-channel or p-channel) and the doping concentrations in the device. For an n-channel MOSFET, the threshold voltage is typically negative, while for a p-channel MOSFET, it is typically positive. The polarity of the threshold voltage can also depend on the doping concentrations in the device.
To determine the polarity of the threshold voltage in a specific MOSFET device, you would need to analyze the doping concentrations and the type of MOSFET being used.
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Hi brothers. I simulated the drop flow using phase field method in COMSOl. After simulations, the flow field inside and outside the droplet is uniform and does not change due the interface. Please see the attached file. I am unable to accept these results because the flow field must be different. Could someone explain this problem either my simulations has some problem or the method?.
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Hi Bacha,
I'm not sure what physics you are using. Comsol needs careful implementation if you have moving/deforming domains. It is possible that you are not simulating/post-processing your results correctly.
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why the surface morphology changes to be uniform after doped of some atoms
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Nowadays, smart electronic devices have become ubiquitous. These devices require power for their functioning. The conventional energy resources are limited in nature, and their consumption produces unwanted byproducts, which cause the greenhouse effect. (1,2) Therefore, there is a need for alternative energy sources that are clean, green, and renewable in nature. The existing renewable energy resources can generate a huge amount of energy, but they are intermittent in nature. Efficient storage of energy to meet the energy demand as and when needed is still a challenge. (3,4)
There are basically two mechanisms of energy storage: one is through batteries, while the other is using electrochemical capacitors/supercapacitors (SCs). (5,6) Both batteries and supercapacitors have fundamental differences due to their materials, structures, and charge-storage mechanisms. Batteries yield a high energy density because of their storing charges in a bulk of electrodes, while SCs may provide high power density via surface charge-storage mechanisms. (1,5−7) SCs have many applications in the field of uninterrupted power supplies (UPS), automobiles, and power backup to protect, enhance, and/or replace batteries. (1,2,7−9) SCs can broadly be classified into two categories on the basis of the charge-storage mechanism: (i) electrical double-layer capacitors (EDLCs) and (ii) pseudocapacitors. (2) In EDLCs, the electrical charge is stored at the electrode–electrolyte interface, while in pseudocapacitors, the charge is stored through redox reactions occurring at the surface of an appropriate electrode. (1) Charge storage via the pseudocapacitance mechanism exhibits some interesting properties as compared to the EDLC mechanism. (1,2,10) For this reason, a lot of work has been done for the storage of charge via the pseudomechanism for the fabrication of high-performance supercapacitive electrodes. (2) Many researchers have suggested that the transition metal oxides can be a potential candidate for supercapacitive electrodes due to the high surface area of the material. (2,9−12) Graphene has also been exploited for supercapacitor applications. (5,13,14) Currently, materials such as NiO, TiO2, Co3O4, RuO2, Ni(OH)2, Sr(OH)2, MnO2, Co3O4, Bi2O, In2O3, and Fe3O4 are being investigated as supercapacitors keeping in view their cost-effectiveness, high capacity, and environment-friendly nature. (1,7,8,15)
Thin-film-based devices have attracted lots of attention, as thin films exhibit physical and chemical properties different from those of the same material in bulk. (16−22) In the case of thin-film and nanostructure devices, the surface to volume ratio is large compared to bulk material. (22,23) The surface morphology of thin films (nanostructure) influences the functional properties of SCs, which play a major role in energy storages. Therefore, a detailed knowledge of the surface morphology is important for the fabrication of devices having the desired properties. (24) Generally, surfaces can be studied using classical parameters (average roughness and interface width), which are highly dependent on the scale resolution of the measuring instruments. However, these traditional parameters are not able to give deeper, nanolevel insights such as the correlation, roughness exponent, height fluctuations, and complex structure of a surface. (24−30) Therefore, we require a technique that is scale invariant. This scale invariance can be achieved by employing fractal geometry. (9,24−30) Fractal objects show a self-affine nature, which can be seen by rescaling the surfaces along horizontal as well as vertical directions with different ratios. (24,25) Recently, Yadav et al. reported a close correlation between the fractal dimension and wettability of a surface. (30) Ţălu et al. have suggested a relationship between the electrical resistivity and fractal dimension. (31) Guisbiers et al. explored the relationship between residual stress and fractal dimension. (32) Wang et al. reported a relationship between the fatigue threshold value and fractal dimension. (33) Foadi et al. studied the roughness-dependent wettability of vapor-deposited metallic thin films. (34,35)
Surface morphology plays an essential role in governing the supercapacitive behavior of the material. An enhanced surface area increases the reactivity. Recently, a fractal study of a Cu-doped Sr(OH)2 thin film as a supercapacitive electrode reported that the supercapacitive value enhances with increase in fractal dimension. (9) This suggests that surface engineering can be an efficient tool to adjust the surface area of electrodes with fractal porosity/granularity for further improvements in the performance of devices. (1,36) It is interesting to note that the electrode–electrolyte interface with fractal geometry offers an improved electrode–electrolyte interface. (1,9,36,37) Fractal objects have a higher surface area as compared to the substrates. (9,38,39)
Many researchers have reported that the performance of a supercapacitor is enhanced with metal doping as well as the formation of nanocomposites. (9−11,36,40,41) Recently, our group reported a high specific capacity (∼413 C g–1), energy density (∼45.95 Wh kg–1), and power density (∼2.6 kW kg–1) in an Sr(OH)2-based supercapacitive electrode. The natural abundance, low cost, electrochemical performance, and environment-friendly nature of this material has made it an efficient candidate that has attracted the researchers to use it as a new electrode for supercapacitors. The supercapacitive properties can be further enhanced by suitable doping of metals such as Cu and Fe. (9,11)
In this work, fractal concepts have been applied to explore the irregularity and fragmentation of the samples. As a test case, we have taken Fe-doped Sr(OH)2 samples fabricated using the SILAR technique. A detailed experimental characterization of the surface morphology, structural analysis, and electrochemical characterization can be found elsewhere. (11) Here, we have focused on their theoretical investigations using fractal characterization. Our study suggests that the Fe doping affects the roughness exponent and fractal dimension. The fractal model will maximize the electrochemically active surface area and minimize the energy loss during the transport of ions inside the fractal networks.
Please check this DOI for more DATA :
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I am facing the problem in dispensing test and control lines. Dispensing is not uniform and appears as spots in some places. This is may be because of hydrophobic nature of the NC membrane (non blocked). currently I am using 10mM phosphate buffer pH7.4 buffer for dispensing the Ab on to the NC membrane. Can some body help me with the composition of Ab dispensing buffer ?
Thanks
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Change NCM supplier
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Do plants grow in uniformity or exponentially or randomly?
What about growth in human body and animals?
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What does Uniformity of drug (tablet or Capsule) means? And what can cause make the uniformity of tablet to be Out of approved specification?
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Uniformity of drug refers to the consistency in the dose and physical characteristics of a drug product, such as tablets or capsules, within a batch and between batches. This is important because variations in dose and physical characteristics can affect the safety and efficacy of the drug, as well as its stability and shelf-life.
There are several factors that can cause the uniformity of a tablet or capsule to be out of the approved specification:
  1. Poor mixing or granulation: If the ingredients of the tablet are not properly mixed or granulated, there can be inconsistencies in the distribution of the active ingredient and excipients, leading to variations in the weight and dose of the tablet.
  2. Inadequate compression: If the compression force applied during tablet manufacturing is not consistent, the tablets may have different weights and thicknesses, leading to variations in the dose.
  3. Improper tooling or die design: If the tooling or die used to manufacture the tablets is not designed properly, there can be variations in the weight and shape of the tablets, leading to variations in the dose and physical appearance.
  4. Poor storage conditions: Exposure to extreme temperatures, moisture, or light can cause changes in the physical appearance and stability of the tablets or capsules, leading to variations in the dose and physical characteristics.
  5. Aging of the ingredients: Over time, the active ingredient and excipients in a tablet or capsule can degrade or change, leading to variations in the dose and physical characteristics.
It is important to ensure the uniformity of drug products in order to maintain their safety and efficacy, and to ensure that the intended dose is consistently delivered. Any deviations from the approved specification should be thoroughly investigated and corrective actions taken to prevent future occurrences.
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Dear Folks/Experts,
I would like to know what are the factors may cause uneven or more water contents in lyophilized vials (most of the vials meeting acceptance limit few vials shown too higher water contents).
20mL vial size and 1/3rd is fill volume (Shelf temp vs set are meeting and vaccum found set limit)
Thanks in advance!
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On the assumption that the content of all the vials is, truly, identical, i.e. no pipetting error, all fills assured by weight, then the are a few things to check:
1. distribution of the vials - are they edge or centre of the pack? Centre dry last so if all the problem vials are in the centre, then more time in primary drying is needed.
2. uniformity of the vials - moulded vials can have very variable bases, which can affect drying (heat transfer through the base from the shelf). If using a tubing type vial, should not be an issue. If moulded vials are the problem, again extending primary drying is needed.
3. if none of the above, then more time, and perhaps a higher temperature in secondary drying should solve the problem. That is, unless there has been some defect in primary drying like a vacuum excursion that caused meltback of the ice ...
A good overview on freeze dyring can be found here:
Kind regards
Rob
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  • Which criteria should be considered in order to distribute the copper thickness homogeneously (uniformly) while copper plating is done by electrolysis?
  • We want to coat the copper film as uniformly thick as possible on a flat metal bar. What should we pay attention to?
  • What is your suggestion for a book/article about this?
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Thank You Mohammad. I will read the paper.
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Polystyrene is a standard polymer ordered from sigma; the pellets size is around 3 mm, and I want them in powder form of uniform size. Please suggest any appropriate method for it.
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1. Use a cryogenic grinding system. This system uses liquid nitrogen to freeze the polystyrene pellets, which makes them brittle and easier to grind into a fine powder.
2. Use a hammer mill. This type of mill uses high-speed rotating hammers to crush the pellets into a fine powder.
3. Use a jet mill. This type of mill uses high-pressure air to grind the pellets into a fine powder.
4. Use a ball mill. This type of mill uses grinding balls to crush the pellets into a fine powder.
5. Use a vibratory disc mill. This type of mill uses a vibrating disc to grind the pellets into a fine powder.
6. Use a pin mill. This type of mill uses a series of pins to grind the pellets into a fine powder.
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I'm going to make a graphene aerogel-coated electrode that substrate is copper foam, but I can't coat a uniform layer of it in the case of loading less than 5 mg slurry. I would appreciate it if you share your experiences about this matter.
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You can use drop casting, spin coating
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I am working on circular array design and am looking for a code that can implement constant beamwidth along frequencies for Uniform circular array. In the code, I tried to use this paper https://israelcohen.com/wp-content/uploads/2018/05/SP_Jan2017.pdf to implement constant beamwidth along frequencies for Uniform linear array, but I found difficulty to continue since I am a new in array beamforming design. Any person can help me with the code implementation for constant beamwidth of wideband frequencies for Uniform circular array? The frequency range is between 0 and 8000 Hz. It will help me a lot
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Okay, but please do you know any code for constant beamwidth of circular array? Thank you for your answer again
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I understand that LPCVD process is surface-reaction limited due to the high diffusivity of the gas, but why does this help with depositing more uniform film?
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This cannot be simply answered without detailing the process, but maybe a very general answer is low pressure = fewer nucleation sites and, thus, more homogenous growth.
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Dear Research Gate members
I have recently read a meta-analysis study in which the authors claimed they have extracted data from original articles in prespecified uniform tables with Epidata software. Does anyone know this software and its usage in meta-analysis studies?
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Epidata is an open-source field epidemiology software suite developed by Doctors Without Borders.
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What is your opinion on the following two sentences contained in the note Uniform Space fom Knowino and Cityzendium?
"While uniform spaces are significant for mathematical analysis, the notion seems less
fundamental than that of a topological space.
The notion of uniformity is auxiliary rather than an object to be studied for its own sake (specialists on uniform spaces may disagree though.)"
They do not know about the works of Pervin (1962), Hunsaker and Lindgren (1970),
Fletcher and Lindgren (1982) on Quasi-Uniform Spaces, and the several former and recent papers on Relator Spaces by me and my coauthors?
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M. Muger, on page 12 of his book, Topology for the Working Mathematician (2022), writes:
"The biggest omission probably is the theory of uniform spaces. Since they
have very few uses outside topology proper, the author is not entirely
convinced that they belong to the core that 'everyone' should know.
Also, there are many good expositions of the subject to which we would have nothing to add Cf. [298, 89. 157, 153], etc."
According to this definite opinion, for intance, the enormous theory of
quasi-uniform spaces is nothing.
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I've been working on the single-chamber microbial fuel cell for more than six months. The major problem is that after fitting the whole setup, the cell showing a potential value 0.0 V even after changing different types of electrodes. The cell setup contains a carbon cloth anode and platinum-coated carbon cloth cathode separated by a nafion 117 membrane. I'm attaching the video of cell .
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Please carefully investigate other factors as well such as nature of electrolytes, inoculation source. Also double check the potnetistate whether is it working properly. Hopefully you will able to get something. Reevised it carefully and carefully see each step.
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Hello, I supervise research on bedridden garments. I need someone who is specialized in this regard, maybe a doctor, to tell me, can we use the word 'patient' for a bedridden? Or, rather it depends on the reason why s/he has become bedridden? Any thoughts?
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I have never heard anyone referred to as "a bedridden". I would think that people who are no longer able to be independently mobile as "people with mobility issues." There is a movement here in the US to use "person first" language when describing challenges or disabilities.
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I supervise a research project on garments for patients with special needs (specifically bedriddens or long-term-care patients). My student insists that they are essentially adaptive garments, and I am not quite sure that they are. I would think of adaptive garments as ones for people with disabilities for example. But, garments for bedriddens would be something in between medical and adaptive somehow. Any thoughts on that? Would anyone who has experience in this regard be interested in helping us on this project?
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Clothes that adapt to changing climatic conditions, such as temperature, are called smart clothes, Or covering the surface of the product with a gel material with specifications that change with the change of temperature
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During the extrusion of the Aluminum 5052 alloy billet, I need to know the following relationships for a smooth uniform and defects-free inner surface of the extruded tube.
1. Bore diameter of the hollow billet Vs the mandrel diameter (bore should be smaller, equal or greater than mandrel)
2. Bore diameter of hollow billet to the length of the billet.
3. Outer diameter to Length ratio of the billet
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without proper dimensional inputs (billet dia, required dia, number of passes, required surface finish in microns, etc) ... it is not easy for anyone to answer your question ...
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Please, I can't understand this sentence: High thermal conductivity to obtain rock with a uniform temperature, and thereby avoid fracture caused by heterogeneous dilation.
any Ideas
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The answer is very simple. If the material has a high trhermal conductivity, its temperature will uniformize very rapidly, i.e. all regions of the material are at te same temperature and have the same coefficient of dilation. If the thermal conductivity is low and there is a heat source at one end, the temperature there will be higher than at the other end of the material. The coefficient of dilation differs from region to region. If two adjacent regions dilate in a different way, the material may break (fracture) at the interface.
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I am trying to build a setup to cure magnetic powders in a polymer matrix in a uniform magnetic field to align the particles in certain orientations. What would be the a setup to do this? In literature I do see some researchers use electromagnets and some use electromagnets. What would be the proffered method in terms of having control over the field being applied?
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James E Hanson Hi Professor, I have tried using permanent magnets the issue is with PM is that the field intensity is non uniform and it tends to pull the powders out of the matrix. I find that most people in literature for magnetorheological elastomers tend to use electromagnets but I am unsure how they are able to cure their polymer matrix as the uniform fields even in electromagnets is within a very small region and it doesn't seem like it could accommodate anything to apply heat for curing to occur. Furthermore they test these smart composites using DMA or rheometers again for which they would need to apply magnetic field over a considerable area to measure change in the young's modulus of the smart composite. I have read about a PEM-1022LS magnetic system in some of the literature but could not find any info on what this system is online any chance you have heard of this?
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In my experimental work i needed to source give me non uniform heat about avery small area
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A laser heating device should allow you to focus the heating area and vary the power. A CO2 laser would be the typical apparatus, but most any laser with variable power output should work.
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Hi All,
I'm looking for the possible methods in measuring the response of chytrid fungus cells to environmental stressors in separate generations. As Lee Berger (2005) claimed, chytrid needs 4-5 days at 22 C to complete its life cycle. But it seems that we have cells in various stages and it is difficult to have a uniform population of fungi cells in a particular generations. So, my questions is that how possible it is to conduct a multigenerational study (for instance 4 generations) in the culture (in vitro) to see the potential impacts of stressors through generations? measurements in separate generations are important in my tests.
Hope that does make sense, otherwise, ask me.
Thanks.
Milad
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Could try calcofluor. Acts as a vital stain.if you wash it out after exposing one generation, maybe subsequent generations would not carry the stain.
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I've already finished a synthesis of a zeolitic material and did the N2 physisorption analysis. Have the product with more hysteresis, more uniform pore distribution?
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In general, it is difficult to have a strong interaction between hysteresis and pore distribution. A sample can have one or many predominant pore sizes and, as a result, a few maxima in pore distribution.
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Are you with or against mass production, and Why? Taking just clothes as an example; why do brands manufacture in eastern Asian countries?
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Fast fashion is not meant in the question; as fast fashion does jeaprodise quality in order to cycle its business through garment recycling under the name of new fashion!!!
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I am trying to apply PBC to a 3D shell model that experiences a uniform deformation in pure quasi-static compression in abaqus and having a hard time finding references that explains retained and dummy nodes. Does anyone know any resources that would help explain how retained nodes are decided for 3d uniform quasi-static compression?
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Thank you Mohammadreza moeini
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I obtained a soil Cu to be 97.56 with a Cc of 0.48. I am confused because using Cu, the soil can be classified as well-graded, but it will be classified as poorly graded with the Cc. Anyone with a better idea of how to classify such soil should please explain.
Thank you.
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Interesting question.... KINDLY CHECK THE FORMULAR FOR EITHER CU OR CC....
IF YOUR ANSWERS ARE TRULY CORRECT I WILL URGE YOU TO STICK TO ONE... CU.... AND YOU WILL BE OKAY.
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Why do cockpit windows often appear to have a rainbow ‘tint’?
It’s similar to what you would see when looking at a shallow puddle of water with oil on top. Here is an example of a Airbus cockpit window with the same rainbow effect:
Thin-film interference is a natural phenomenon in which light waves reflected by the upper and lower boundaries of a thin film interfere with one another, either enhancing or reducing the reflected light.
It's the same mechanism behind your oil example. The thin film in this case is the heating coating applied to the windshield, which is intentionally non-uniform (explained below), making the effect even stronger.
Fringes observed on a windshield due to thin film interference caused by a conductive lm deposited on the window for electrical defrosting/defogging.
The fringes are strongly visible because the thin film thickness is highly non-uniform on purpose: as the voltage is applied on two opposite points of the window, a uniform conductive film (uniform sheet resistance) would lead to non-uniform current density, and non-uniform defrosting. Some window parts, especially on the sides and far from the electrical contacts, would dissipate less heat, and defrosting would be significantly less effic
**But the main question is which of these coating methods can create such a non-uniform design (in terms of thickness) on glass substrates with irregular geometry?
According to Figure (windshield), a non-uniform thickness of the deposition layer is applied to the windshields of the windshield aircraft.
We really need your help and guidance.
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These colours are also visible on the large windows of buses. May be it's a property of the multilayer (different polymers) window and not related to the ITO.
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As the question is, in many natural gem stones, the color distribution is not uniform, so is there a suitable method to separate and quantify the color clusters?
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Ziyuan Lau!
输出表单的截图:)
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The two notions of Compact and Sequentially compact are identical in metric space. I want an example of a compact uniform space that is not sequentially compact.
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Uncountable product of [0,1] is a compact topological space which is not sequentially compact. This space is uniformizable being a completely regular space.
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Flow through a Petroleum Reservoir
1. Do we have a ‘dynamical equilibrium’ existing between inertial and viscous forces and those due to external body forces and the internal distribution of fluid pressures – towards defining the velocity distribution – across the (vertical) thickness – associated with ‘Flow through a Petroleum Reservoir’?
If yes, then, why do we have uniform velocity distribution in Petroleum Reservoirs – as against the Parabolic Velocity Distribution (along the vertical section - normal to the flow direction)?
If not, then, how do we characterize the coupled effect of positive pressure (average reservoir pressure) and negative pressure (capillary pressure) responses – simultaneously - associated with a petroleum reservoir?
2. In the absence of an explicit ‘gravity’ (and density) term – in original Darcy’s equation, whether the replacement of ‘hydraulic head’ by ‘pressure head’ remains justified?
3. In the absence of a suction head or a negative head in original Darcy’s equation, can we afford to modify the fundamental physics itself – by bringing in the ‘Capillary Pressure’ – and still get Darcy’s law extended?
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Hi Suresh and all.
Only under static conditions, capillary phenomena are fully understood. As soon as the meniscus (interface between immiscible fluids in a capillary) start moving, its curvature changes, viscous dissipation occours and the surface energy associated with the interfacial tension between fluids also changes. Depending on the flow direction and the prevailing pressure gradient in the porous medium, meniscus curvature can reverse. For a given capillary, two expressions for Darcy´s law would hold simultaneously in different sections. Presently the phenomena are poorly understood. Check “dynamic capillary effect”.
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Normally F1 plants suppose to be uniform both genetically and phenotypically and start segregating at F2, but I notice some differences in seed germination and seedling vigor (all things being equal) WHY?
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Dear Aminu Moriki Ladan it depends of the number of parents involved in mating and their genotype. If either female and male parents are clones, F1 should be genetically uniform, at least external factors occur (mutations, contamination,...). However, if parents aren't clones, variations must be expected.
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!!!: In below link, you can read it more convenient way.
I have a question of continuity equation for LES with uniform filter. I've heard that in uniform filter, 📷 And I want to know why. In the uploaded figure, there is my guess. What I guess is if 📷, then it means that 📷. And this means that 📷. And this can be reasonable because the spatial trend of 📷 and 📷 is very very similar for uniform filter. (Because LES generates very fine mesh in comparison to RANS, it can imitate the similar graph to 📷 which means the real velocity in real world.) (📷) Cause of filter, velocity value can be little different between 📷 and 📷. (ex: 📷) And also value of 📷 can depends on which weighting function user choose. But the spatial trend of them(slope of graph, differentiation with respect to x) can be very similar. In conclusion, I've guessed that in uniform filter, 📷 can be satisfied at first and we can see it from slope of graph. So 📷 is zero. Here was my guess. Is this guess reasonable? or is there any other reason why 📷 is zero?
Thanks :)
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Now I've got it.
Here is my note and I think it can help this question.
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I am working on loads such as snow load, and I was wondering how it is achievable to assign a uniform horizontal projected load to a spherical shell (i.e. not applied to the reference surface)?
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Can you share your Abaqus model (.inp)?
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Proper cleaning process of Carbon cloth before using as an electrode in electrochemical experiments.
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Pijush Kanti Gan The primary reason for acid treatment of Carbon Cloth before using them for electrochemical purposes is to avoid any contamination (inert surface), and to develop proper adhesion between the inert surface and active material.
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Together with some dear colleagues we are working on a new project. what do you think about the relationship between green chemistry and circular economy models applied to the clothing industry?
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When using buffers to maintain pH for sorption isotherms using natural waters, we are seeing a pH shift of 0.25 over a 24 h reaction. Are there ways to keep the pH more uniform than this?
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One thing that we're also concerned with in using Good buffers is the formation of hydroxl radicals and their impact on redox chemistry. For our alkaline system, what appears to be a good option is the CHES buffer (pKa 9.5).
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I want to assess performance of a 4 and 5 antennas (arranged in the form of circular array), by calculating different parameters such as CRB and RMSE. However, as I have seen in theory, a number of different formulas and methods are implemented. Moreover, what I learnt till now is that you have to deduce a different CRB formula for different scenario. Is there some basic guide or some instructions which can point me in the right direction for calculating CRB as per given antenna design?
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It mean if math. formula is complicated, try some thing else, outcomes of tryout is a data, the standard deviation of data has the same meaning of RMS. GOOD LUCK
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If $X$ is a Hausdorff completely regular space and $E$ a Banach space, what are the extreme points of the unit ball of the Banach space $C_b(X, E)$ of all bounded continuous functions from $X$ into $E$, with the uniform norm ?
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To the best of my knoeledge, the problem remains open in the more concrete setting of linear operators between Banach spaces, endowed with the usual operator norm. It may sound strange, but even the finite-dimensional case remains open! I have personally studied the problem, along with some co-authors, exclusively in the Banach space context, and mostly in the finite-dimensional case. I think that it is a particularly hard problem, even in this far more restricted scenario.
Without a shadow of doubt, the problem deserves far more attention from the functional analysis community, and therefore, I must thank you for focussing on such a simple yet deep question.
Having said all these, I do know of some interesting results by Lindenstrauss and Perles, Lima, Sharir, T. S. S. R. K. Rao among others on this topic. It might be fruitful to look into their ideas and results (again, mostly in the Banach space context). We have also tried to contribute something to this intriguing topic. We (Paul, Mal, Sain) we have obtained a complete geometric characterization of extreme contractions between two-dimensional strictly convex and smooth Banach spaces. We (Paul, Ray, Roy, Bagchi, Sain) have also been able to obtain some interesting conclusions on extreme contractions between polyhedral Banach spaces. Recently, with Paul and Sohel, we have also obtained a complete characterization of extreme contractions between finite-dimensional polyhedral Banach spaces. Most of these papers are available on RG and please feel free to look at them, should you choose to!
Of course, much remains to be done on this fascinating question, and from multiple points of view, including analytic, grometric and combinatorial. In short, a potential exciting journey into the unknown!
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I am preparing ZnO thin film by the chemical bath deposition method. Although I have worked with several parameters and tried many times to have a uniform film I am not able to form a uniform film yet. Please give me some suggestions about how do I make the film more uniform in the CBD method?
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I recommend trying to follow methods from existing literature as closely possible. Works that have been highly cited likely have repeatable methods. Without knowing exactly what parameters you are experimenting with, it's hard to say exactly what the issue is. Certainly the concentrations, pH, temperature, and substrates all play a role. Please see these two papers, and I recommend some additional literature review to find more.
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How to avoid precipitation (or) How to get Uniformity of final liquid laundry detergent solution? we always get small amount precipitation after few hours. How to solve this problem?
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Hello sir,
Could you please tell me what method did you use for the formulation?
Do Check out if the method needs improvement.
Other than that, You can check out the possible reason causing Precipitation.
It can be either due to the
1) formation of insoluble complexes
or
2) two oppositely charged particles leading to electrostatic attraction clubs together
or
3) complexes interact with one another and form a neutral aggregation
or
and consequently results in precipitate
Please take a look at these articles, It may be useful!
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How to have a uniform CuO thin film using dip coating method after synthesizing CuO powder?
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You can synthesize CuO and Cu2O thin films using chemical vapor deposition techniques. https://doi.org/10.1002/pssa.201127493
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I need to prepare 0.3mm PE compression molded sheet, but I have issue with thickness uniformity. I will be thankful for any technical advice?
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Dear Mehrnoosh Ezzati Givi, why not via blown-film extrusion. In case you insist on compression molding, it will may be possible if the granules/pellets are metled first between two PTFE sheets, then apply pressure. My Regards
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Dear colleagues,
I would need the following document to validate the cleaning and sterilization process of re-usable gwoning. If someone could send it to me it would be great!
EST-RP-CC003.3 Garment System Considerations for Cleanrooms and Other Controlled Environments
Thank you in advance!
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I could provide you with CC003.4.
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Colors are weak features from computer vision. But, the colors are widely used in video-surveillance and search of objects. However, currently there are pieces of clothing and vehicles that change color automatically or manually, for example, cars. What will be the future of colors as features in machine learning?
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Changing colors is restricted due to its high cost. However, features can be extracted using different parameters based on grey-scale or binary images.
The license plate can be used for vehicles, and the face or gesture can be used for people.
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I want synthesize TiO2 nanoparticle with uniform size range of less than 10nm. Can anyone share the recipe with sol-gel method?
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Dear all, please have a look at the following free access documents. My Regards
DOI: 10.5772/intechopen.75425
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I am reading the book entitled “The Victory of Reason”, by Rodney Stark, and he points out that “The First Industrial Revolution was not a revolution at all but an evolution of invention and innovation that began in England perhaps as early as the eleventh century.” Is that true?
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One of the cities at the forefront of Cloth-making industrial revolution was Leeds which is said th have beem built on Wool.
Ref: https:// www. historic_UK.com
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Hi. anyone can help me on how to coat a carbon felt and carbon cloth with a platinum plate. i have as a plate, not powder. can anyone help me with the protocols?
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Dmitriev, D. S., N. A. Khristyuk, and V. I. Popkov. "Electrodeposition of α-Ni/β-Co composite coatings on the carbon felt: Structural features and electrochemical performance." Journal of Alloys and Compounds 849 (2020): 156625.
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Seed germination
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Speed of germination= å x/N
i.e. X1/n1 + x2/n2 + x3/n3............. xn/Nn
Where, X = no. of normal seedling; N = no. of days
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There are institutions in many countries where students wear unisex uniforms. Some educational psychologists and human rights activists believe that such decisions will decrease gender discrimination to a certain extent and will help give women enjoy equal status in society. However, people, especially with an orthodox mindset, oppose this type of liberal movement, saying that this will denigrate the status of women. What do you think?
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In fact It is very frequent to think that equality means identity. But equality us about rights, not about being different in our identities. Being a man or being a woman means different identities with equal rights. So It is not a problem at all to wear different uniforms, if the curricula and the treatment are equal for both, girls and boys.
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I am doing a graduation project about a recommendation system that recommend your outfit from the clothes you have in your wardrobe but I am struggling on what is the best way to create a system like that And i Would like your help.
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I would first sit down and describe at a high level the features that are desired for each of the modules. Be sure to account for feature dependency between modules. After doing so, the stage for particular algorithm that targets the different features can be derived. You can contact me here or privately to continue the discussion.
Regards
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We're accustomed to thinking that tool use is what distinguishes us from our non-human cousins, but is that really true? We see other species using "tools" and crude technologies so I don't think it is the defining factor. Perhaps it's actually the use of clothing that is the greatest difference. I'd like to know if anyone has done research in what I will call sartoriology.
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Clothing or creation of body covering probably correlates with the loss of body hair and the necessity of keeping warm. At the same time, perhaps, the use of fire began as a source of warmth. So the use of clothing and fire together perhaps sets humans apart.
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I am testing the anti fungl activity of two actinobacterial strains how can I uniform the inoculum of the 2 strains
how I can make the same concentration
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To uniform the inoculation, you have to apply the same number of spores. You can culture the actinobacteria in solid media and after spore formation drags the spores with a spreader with some water. After making a spore-water suspension, you can count the numbers by using neubauer chamber under a microscope. The spore count method is easily available on the internet.
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I am testing the anti fungal activity of 2 actinobacterial strains how I can uniform the inoculum
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To uniform the inoculation, you have to apply the same number of spores. You can culture the actinobacteria in solid media and after spore formation drags the spores with a spreader with some water. After making a spore-water suspension, you can count the numbers by using neubauer chamber under a microscope. The spore count method is easily available on the internet.
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I am preparing liposomes using the thin film hydration method. The lipid I am using is DPhPC (no phase transition temperature between -120/ 120 C). Briefly here is my protocol
I first dissolve the lipid (only DPhPC) in Chloroform (1 mg/ml) using a round flask. Then I dry the chloroform with nitrogen. The dried lipid film is then placed in a vacuum chamber for 8+ hrs. Afterwards, 1x PBS solution (1 ml) is added to the flask and the solution is allowed to hydrate at a temperature of 65 ⸰ C under vigorous stirring with a magnetic spin bar for 2+ hrs.
My problem, is that after chloroform evaporation, a non uniform white residue appears on the wall instead of a thin uniform lipid layer. Also, during hydration the dried lipid is not breaking into smaller pieces and remain as large aggregates (see image attached) which is not possible to extrude and sonication does not help. Any idea on why hydration is not properly occurring?
note: The attached image is taken after 2 hrs of hydration, it shows the large precipitate of lipids in 1xpbs.
Thank you in advance,
Rami
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First of all, how fresh is your DPhPc?
Properties of diphytanoyl phospholipids at the air-water interface by Yasmann and Sukharev (DOI: 10.1021/la503800g) use a similar method to prepare DPhPc liposomes with some slight, but significant differences. Consider them when comparing with your methods.
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Hi
I want to produce a graphite and aluminum silicate based water solution as a refractory coating. Which binders and additive are proposed? The rheology and uniform coat with no drips are required.
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The concentrated phosphoric acid as a binder can be combined well with fine alfa Al2O3.
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Hi, I have been working on immunoblotting using animal tissue samples. Although all experimental conditions are uniform, however, sometimes the protein expression between replicates varies. Need kind suggestions to fix such issues.
Thanks
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Thanks all
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Hello everyone, I am trying to redistribute moment over a 2 span beam when a uniform distributed load is applied. I have placed a hinge at the interior support to monitor the maximum negative moment developed in the beam. When I run the analysis and look up hinge results, it shows that the rotation value exceeds the one I calculated from hand calculations. I am unsure about how to fix this.
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Just a quick check; are you modeling in plane or 3D?
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Hello!I have a strong desire to get some recommendations on papers about something like interactive digital textiles. I’m a sophomore student in china, and my major is Artificial Intelligence. I am going to enter the laboratory for internship,and some garments such as project jacquard has fascinated me so much. I gonna do a presentation or just write a summarize about this field ,which is really cool!
In a nutshell, I sincerely seek your help.Thank youuu so much!
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I would like to know if it is possible to have a uniform doping over 2 µm for n-type crystalline silicon, using the ion implantation technique, in order to create a BSF layer in a solar cell.
I thank you in advance for any information that can help me.
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Thank you so much Hadi Jabbar Alagealy for your valuable answer.
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Hello, I hope you are all well. I am finishing my MSc and am struggling quite a bit with organising/ analysing my data.
I have conducted a study looking at the effect of different model sizes on the recall of clothing advertisements. First, participants were exposed to 45 images of clothes on 3 different types of models (Thin, average, plus = 15 in each). They were then shown images of the clothes the thin/average/plus size models wore + some extras (15 in each) and required to indicate whether they have seen them before. Lastly, we asked them to input their BMI (split into thin, average, plus).
The aims are as follows: 1) to determine whether the diversity of the model impacted recall 2) whether a higher percentage of recall occurs when participants view models of the same BMI. 3) whether people recall more for thin vs other
Unfortunately, the participant BMI split is very uneven, with most being average - this makes it hard to test the second aim.
i hoe this make sense :) any help is very appreciated!
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First, identify your dependent (DV) and independent variables (IDV).
After that, check the type of your variables- categorical( nominal and ordinal) or Continuous ( ratio or interval).
Now, check whether DV and IDV are parametric (metric) or not. [Otherwise, they are non-metric (non-parametric)]
if variables are non-metric (both DV/IDV) then apply crosstabs (chi-square).
if DV= metric and IDV= non-metric, use hypothesis testing.
if DV= metric, IDV=metric; use Correlation and regression.
if DV= non-metric, IDV= metric, use discriminant analysis or binary regression.
N.B.: Above mentioned techniques are for Bi-variate analysis.
Apart from that, you can use mean, median, mode counts, and percentages. (For univariate analysis).
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I want to model uniform donor type defects in the material throughout the bandgap in Silvaco. There are some examples for Gaussian and exponential defects in the Atlas manual, but I couldn't find anything related to model uniform defects.
Please help me for the same.
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I do not know if there is a delta function distribution delta(E-Eti),
where Eti can take the values you intend. You can also assign them the concentration you need.
If there is no such function you can choose the Gaussian distribution function
Nti exp (E-Eti)^2/sigma^2
with sigma very small to mimic approximately the single level traps.
Best wishes
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While I understand the validation parameters and the procedures for assay AMV, I do not get the concept for determination of Specificity and Method Precision (Repeatability) for content uniformity.
Appreciate it if someone who has done AMV for content uniformity of tablets/capsules to answer my question. Thanks.
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The content uniformity is in fact an assay method with additional dose testing, thus content uniformity. There is an accuracy number for n>=6 and the associated relative standard deviation that need to meet the acceptance criteria.
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Hi, for my graduate research, I need to analyze a simple bolted connection on ABAQUS. The bolted connection consists of 3 bolts that connects 3 plates (see the picture attached for reference). The top and the bottom plates, is fixed at the end of the plate. The middle plate is loaded with uniform loading on the other end. I've tried to run it, however I get these kind of error
***WARNING: THE SYSTEM MATRIX HAS 3 NEGATIVE EIGENVALUES.
***WARNING: DISPLACEMENT INCREMENT FOR CONTACT IS TOO BIG.
I have tried to make the surface contacts each other in the beginning of the analysis, however it still doesn't works.
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Hi, this is the .inp file, Thankyou
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I have synthesized a pressure-sensitive adhesive containing 37 % butyl acrylate and 3% acrylic acid and sodium lauryl sulfate as surfactants in nitrogen atmosfer. After synthesizing, I noticed that the adhesive forms an island shape on the surface of the pre-treated propylene film, and the adhesive film is not uniform.
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Dear all, in addition to the valuable answer of Prof. Frank T. Edelmann, I think it is difficult to screen the reasons regarding the multiple variables involved, but I strongly suspect the uneven surface modified polypropylene. This means a surface characterization should be done first. My Regards
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I'm doing work with camphor oil. Prepare its microcapsule and trying to bind it with the cotton material. After the formation of capsules, I need an adhesive to bind it with the cloth material.
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PU binder is higly effective in the application for cotton fabric. The effectiveness also depends on the shell material you used for microcapsules.
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I am synthesizing gold nanoparticles from some green source but every time I am getting nanoparticles having different shapes like triangular, hexagonal, pentagonal, rod-shaped all in a single image and also with different sizes...can anyone suggest to me which factor I can change to get uniform shape and size? I have found in some literature that changing the concentration of reducing agent, reaction temperature and time can help in getting uniform shape and size...is there any other factor that can also need to change? I will be very grateful for your kind suggestions.
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I am currently using a 20uL tip to create scratch but apparently, with every new biological replicate exp, I do not get uniform or similar scratch as the previous exp. Any hacks/tips on how to achieve a uniform scratch every time? Also, Pls recommend the best tool/software to accurately measure the widths? Thank you.
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Hello Ankit Naik
I used to do the scratch with a 20μl tip and it is always going well. Here are some tips that may help:
if you do the assay using 6 or 24 well plates, you may use the plate cover as a ruler during scratching.
don't twist the tip and try to fix the angle between the tip and the plate during scratching. it is better to run the tip over the cells once. regarding the second part of your question, ZEN Blue Software is doing well and you can set it up with your inverted microscope camera https://www.zeiss.com/microscopy/int/products/microscope-software/zen-lite.html
you can also use any photoshop program, in this case, the width will be in pixels.
these may help you to optimise your assay
In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro
Good Luck
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I have a commercially available cloth whose fiber composition is wrong. Therefore, I need to find a testing lab with an expertise in identifying fibers. The cloth is likely a fiber blend, so the tests should also be able to tell me % of each fiber type identified.
This work is for a product in development, so a fast turnaround is also a must.
Thanks for you help!
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Thank you for the replies.
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Hi Everyone,
I'm currently practising an object detection model which should detect a car, person, truck, etc. in both day and night time. Now, I have started gathering data for both day and night time. I'm not sure whether to train a separate model for daylight and another model for the night-light or to combine together and train it?
can anyone suggest to me the data distribution for each class at day and night light? I presume it should be a uniform distribution. Please correct me if I'm wrong.
Eg: for person: 700 images at daylight and another 700 images for nightlight
Any suggestion would be helpful.
Thanks in Advance.
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Ben Harper, thanks very much for your recommendation.
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I am doing research on Iron Age clothing in the Netherlands for a living experiment that is being organized by the Dutch History Youth Association (Nederlandse Jeugdbond voor Geschiedenis). In Dutch and German books on Iron Age clothing it is stated that women wore a peplos. Sadly these claims are never backed up by any archaeological evidence. On the internet I can't seem to find any evidence either. Is there any one that knows on what evidence these claims are based?
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Hi! You have the Iron Age peplos from Huldremose, Denmark. https://commons.wikimedia.org/wiki/Category:Huldremose_peplos
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Hello, I am doing PCR on fungal DNA samples and use EF1 and EF2 primers and the New England Bio Labs Phusion Taq Polymerase. I have had successful PCR reactions but over the past month I have been getting a uniform smear in each well including my negative control. I still have nice crisp bands, but the smear is a problem because I am sequencing these products. I use filter tips and my prep areas for pre-PCR and post-PCR are separate. If anyone has experience with this or any advice, it would be much appreciated. I have attached an image of a recent gel, the first well beside the ladder (farthest to the left) is my negative control (PCR mixture with no DNA, ultra pure water replaces the DNA). I have changed out my reagents/water and the smearing has not stopped.
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Some prevalent errors might cause the PCR product to get bogged down below:
  • Misread gel: If the gel is not poured correctly, it will not polymerize or harden uniformly so that the molecules smear.
  • Well overloading: If the wells are too much packed, or the sample isn't diluted appropriately, the surplus sample might be smeared through the gel. Moreover, when the gel is shifted after placing the selection well, the model might break down. This might be spread as well.
  • Improperly Prepared Sampling. Divides into an enzyme that cuts the molecule in particular areas to prepare the protein or nucleic acid sample (restriction digestion/). If not correctly performed, the enzyme might uncontrollably break down the molecule too much and cause a smear. Moreover, the wrong buffer or temperature choice might lead to an inappropriate enzyme function, producing flushing, and not most minor.
  • Pollution: if a sample of DNA is polluted by a protein, which can also produce smear.
This is a relatively common problem for agarose gel electrophoresis, and there can be plenty of information elsewhere.
Good luck!
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I need a uniform thin film of Teflon on glass. How we can thermal evaporate Teflon using a vacuum thermal evaporator?. Which type of Teflon I may have to purchase for this?.
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Dear Pratheek Mekkat this is a very interesting technical question. In addition to the useful link provided by Bikash Kumar Das please also have a look at the following relevant article:
Protective applications of vacuum-deposited perfluoropolymer films
(see attached pdf file)
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I want to know how I can prepare a composite membrane with uniform pores to separate sea water(water desalination).
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You can check the paper below for the answer:
Good luck!
K
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HEA fabrication
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In most cases high entropy alloys are prepared by melting the constituents together at high temperature. Since the entropy goes into the Gibbs free energy always as -TS, the role of entropy is higher at high temperatures. Many systems (but not all) therefore can be single phase liquid. The fast diffusion at high temperature and in liquid state distributes the atoms homogeneously in a short time. If the high entropy alloy is single phase at room temperature, too, the cooling can be made at medium rate. Attention is needed to prevent segregation of elements during solidification. Some tempering at temperatures just below the solidus temperature may be necessary to homogenise the alloy by solid state diffusion. If the solid state is not single phase a rapid solidification can produce single phase homogeneous alloy.
Another approach is to use powder metallurgy and homogenise the alloy by diffusion of elements during sintering. Homogenbeous distribution can be reached also by atomising the liquid alloy and sintering the powder particles.
A powder approach is also the mechanical alloying of mixed powders. Here the solid state diffusion enhanced by high defect densities can produce homogeneous alloy. However mechanical alloying in most case is connected with impurity pick-up from the milling system or from the atmosphere (oxygen).
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I am modelling an RCC Column in ABAQUS, When I apply Displacement load as point load, it gives good load deflection curves, but all the deformations are in upper portion of the column.
When I change point load to Uniformly distributed load, the deformation of column shifts to center but it totally changes and makes an unrealistic load deflection curve. How to resolve this issue??? how I can get accurate load deflection curve by applying uniform load on column. It seems that column bends in upper portion only?
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