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Hi, I am collecting RP-HPLC data using Shimadzu Labsolutions Version 5.71 SP1.
Every time I do the postrun PDA analysis, I have to manually remove unwanted peaks, e g. below retention time=4.5 min, etc. Basically, I am only interested in 3 peaks, at time=4.5, 6.5 and 11min. Besides, I need to copy the peak table one by one to my excel file for data processing and then graph plotting. It seems that I can only export each LCD data file into ASCII format one by one.
1) Is there anyway I can remove the unwanted all at once for all, say, 40 LCD data files, instead of editing it one by one in the software?
2) Is there any way to bulk export my data? The main purpose is just to ease data processing and cleaning, if it would.
3) Is there anyway to bulk export all forty chromatograms at once?
Thanks
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In Shimadzu LabSolutions Version 5.71 SP1, the terms "Processing Method" and "Batch Processing" may not appear explicitly in the menu, but the equivalent functions exist under Postrun Analysis and Data Analysis. Here’s where to find them:
1. Removing Unwanted Peaks in Bulk
Since LabSolutions doesn’t have a direct "Batch Processing" function, you can apply "Data Analysis Method" to multiple files:
1. Open LabSolutions Postrun
Go to [Postrun] in the software.
2. Set Up a Data Processing Method to Remove Unwanted Peaks
Open one chromatogram.
Click "PDA Data Processing" or "Quantitative Processing" (depending on your setup).
Go to "Peak Integration" and adjust parameters:
Set a retention time filter to only integrate peaks at 4.5, 6.5, and 11 min.
Save this as a New Processing Method.
3. Apply the Method to All Files at Once
In Postrun, go to File → Batch Processing Settings (or "Batch Recalculation" in some versions).
Select all 40 files and apply your saved processing method.
This will automatically remove unwanted peaks across all files.
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2. Bulk Export of Peak Table Data
LabSolutions does not allow exporting peak tables in bulk directly, but you can automate it:
1. Export Peak Table in ASCII Format (For Each File):
Open [Postrun] → [Peak Table].
Click "Export" → Choose ASCII (.txt) or CSV (.csv) format.
This needs to be done per file, but you can automate it with a script in Excel.
2. Automate Bulk Data Import into Excel:
Save all ASCII/CSV files in one folder.
In Excel, use Power Query (Data → Get Data → From Folder) to import all CSV files into one sheet for further processing.
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3. Bulk Export of Chromatograms
1. Export Multiple Chromatograms as Images/PDF at Once:
In Postrun Analysis, go to File → Export Chromatograms.
Select multiple files.
Choose output format (PDF, PNG, JPEG).
If this menu is not available, another workaround is to use "Batch Printing":
Go to Postrun → Print → Batch Print and save as PDFs instead of printing.
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What is the most friendly software for the analysis LC/MS on macos (e.g extension; LCD, mzml)...
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For LC-MS analysis on macOS, user-friendly software options include 1- MZmine: an open-source tool for mass spectrometry data processing, 2- OpenChrom: which supports various chromatography and mass spectrometry data analyses. Both offer robust functionalities suitable for analyzing LC-MS data.
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Hi everyone,
Later this year I will be conducting a repeated measures longitudinal experiment designed to quantify the long-term impact of Mixed Reality displays as user interfaces for viewing flight procedures/checlists on drone piloting performance.
Prior to testing, participants will receive training from instructors, and over the course of this training period, will execute 2 different drone flights (as shown in the image attached as 'Position Flight' and Traverse Flight').
Participants will be randomly assigned into 1 of 2 groups - the 'Hololens First' group, or the 'Screen First' group (an LCD screen is the control display condition). I will also be ensuring that an equal number of participants are assigned to each group.
Following the completion of the training flights, participants will perform three subsequent test flights:
  • Test Session 1 will involve participants executing 2 different flights not seen in training (shown in the image attached as 'Orbit Flight' and 'Recon Flight'), and will take place roughly 5 minutes after the completion of training.
  • Test Session 2 involves participants returning 10 days after Test Session 1 to conduct the same flights they executed in Test Session 1 (Orbit Flight and Recon Flight).
  • Test Session 3 involves participants returning 180 days after Test Session 1 to conduct the same flights they executed in Test Session 1 (Orbit Flight and Recon Flight).
My question, therefore, is do I need to randomise my participants into the Hololens First group or the Screen First group prior to each test (i.e. randomise participants before Test Session 1, randomise them again before Test Session 2, and finally, randomise before Test Session 3), or if it is okay to randomly assign participants to one of these groups prior to their training flights commence - with participants remaining in either the Hololens First Group or the Screen First Group for the entire duration of the experiment?
Thanks a lot in advance for your help - it is much appreciated!
Cian
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It looks like you want to quantify the long term effects of 'Hololens' and 'Screen' relative to each other, and not so much relative to no 'mixed reality display'.
In that case, I think that you need to cross over from 'Hololens' to 'Screen' or v.v. only once: after the third test run. Because if you cross-over after each test run, you'd measure the long term effects of both type of devices at the same time and cannot well contrast the results. And that implies that you can randomize only once.
Does that answer your question?
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Hi,
I was working on a thesis project on a portable ECG device, I checked these
So it was basically biopotential->Amplifier->logging->displaying using Teensy(Programmable chip), Adafruit(Bluetooth Module), SPI LCD Screen, and resistors and capacitors.
I developed and assembled all except Teensy, adafruit, SPI LCD screen, as I don't have circuit on how to connect output to these 3 devices.
Can anyone share some other resources it would be very much valuable.
Thank You
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Dear sir, I guess the Teensy is used to acquire the signal (use one of the analog inputs; for instance, pins for 14 to 23 Analog). The signal is of course converted (Analog to Digital) inside the Teensy. Then, you can display what you read using SPI (pins 10 to 13 of Teens) on SPI LCD Screen. For the Bluetooth device, I don't know what is it used for; maybe to save the data on an SD card and send the data (acquired ECG) to a remote station (computer I guess). You can use it. It is not difficult to assemble that and programs exist for each task: 1. Acquire analog signal using Teensy; 2. Display a value, figure using SPI of Teensy on an SPI LDC display; 3. Send data using a Bluetooth device.
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How do I convert the millivolts' data from the two electrodes (i.e., their difference) which are in the range of 10-200 mV? I want to amplify this data to display it on LCD to a range of 0-5 Volts.
Hi,
I am working on electrochemical sensors, where I need to do the following tasks using Arduino UNO board
  1. To convert the milliVolts signal received from the two electrodes (i.e., their difference) which are in the range of 10-200 mV. I want to amplify this data to display it on LCD to a range of 0-5 Volts. Suggest a circuit and module.
  2. Based on the Voltage displayed, it should tell the concentration of the solution in which our electrode sensors are dipped say 10/100/1000 ppm.
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First, you won't be able to do it on an Arduino Uno because its inputs are not true analog; they are pulse width modulated. I solved this problem by using an Arduino Due, which has true analog outputs and inputs.
Second, you'll just need an OpAmp to add a gain to the voltage signal, and you can also filter out noise at the same time. Calculate the gain you want (from 200mV to 5V gives a gain of 25), then pick the correct OpAmp circuit for the job - I think a comparator would be appropriate here. Simply refer to elec eng tutorials online (like this one: https://www.electronics-tutorials.ws/opamp/op-amp-comparator.html).
Third, the code for showing a readout to your LCD screen (these are standard with the Arduino kits) is also standard, you can find this online in any Arduino forum. Use C+ in the IDE to write a "if...then" for different levels of input voltage to cause a display of either "10 ppm", "100 ppm", etc. That should be easy to do in 3 lines.
The hardest part is getting your sensor to detect the analyte repeatably!
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I understand that the units of
UTh = π ∙ √( Kii / ε0 ∙ ∆ε )
is sufficient, but I can't find a intuitive understanding for this equation.
This is what bothers me, so please tell me what in my reasoning that is wrong:
Let's say that I conduct two experiments testing the Freedericksz transition voltage, using the same liquid crystal, having the same homogeneous (planar) strong anchoring condition,
the same direction of the applied electric field, the same crossed polarisers to monitor the difference in intensity, BUT with two different cell thicknesses. To make my point even more distinguished, let's say that the first cell have a thickness of 5 μm, and the second having a much larger thickness of 5 mm.
For these two experiments I will surely detect two different threshold voltages, a much larger voltage for the 5 mm cell than for the 5 μm cell, because the voltage for each cell corresponds to the necessary voltage needed to produce a sufficient electric field to polarise the LC molecules so they will start to align with the electric field.
However, if I from this threshold voltage calculates the Kii value according to above equation, I will get two different values for the elastic constant for the same liquid crystal and surface interactions.
So, is the Kii value system specific?
Because I know that ∆ε is specific to the liquid crystal material.
I understand that this method of experimentation is sufficient to use as a comparison for different liquid crystals, mixtures and dopants when used within the same system.
But is not the electric field threshold instead needed to be able to use the material within a device?
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The reorientation begins at the center of the LC cell (assuming a symmetrical cell for simplicity). The thicker the cell, the less impact the substrate has on the director in the center of the cell. In the meantime, the local electric field decreases with the increase of thickness at a fixed applied voltage. These two factors (coincidentally) cancel each other out and therefore the threshold voltage does not depend on the thickness of the cell.
However in different geometries (e.g. homeothropic->planar reorientation when the electric field is parallel to the substrate) the threshold voltage may depend on the thickness of the cell.
The elastic constants (Kij) are material specific and are commonly treated as constants if the temperature is fixed.
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I am interested in commercially available liquid crystal displays for use as a spatial light modulator in a custom-designed video projector. Where can I buy such LCDs?
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Dear All,
I could not find any satisfactory answer on Internet about working principle of ultrasonic milkanalyser. What it does is , you have to put a small sample cup of about 30ml then a peristaltic pump sucks the milk in and hold it in a sensor , ultasonic, which then heats it to 40*C and ultrasonic waveform are transmitted from one end of sensor and collected at other end then waves are analyzed by a central mincrocontroller then temperature is raised by 20*C and same analysis are done at 60*C temperature. And then these parameters of milk are displayed on a LCD , Fat in % (0-10), SNF,Solid non Fat(0-15) %, Density in g/ml and others these are calculated with mathematical calculation Lactose, Salt.
I am attaching a hand made diagram of this also.
What I wanna know how these reflected waves are analyzed , what's the algorithm?
Thanks & Regards
Rajeev J. Mehndiratta
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Hi, My paper
  • Principles of Ultrasonic Technology for Treatment of Milk and Milk Products
  • Effect of Ultrasonic Treatment on Buffalo Milk Homogenization
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I have been having trouble finding hourly Solar Radiation data for any land-based weather stations in northwest Florida. I have tried looking at the NOAA LCD data but they do not appear to have hourly solar radiation included. Does anybody know of potential sources of hourly solar radiation data for land-based stations? Does anybody know of any public organizations in Florida that may manage weather stations throughout the state?
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I fully agree with Reuben. The National Solar Radiation Database (NSRDB) is an excellent tool. Within the NSRDB, are several data sets. I am unsure of the existence of recent measuring stations in your area. Nevertheless, you may use the so-called Physical Solar Model (PSM) data set which results from a processing of satellite observations and models. Hope it helps. Best regards. Lucien
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not arduino
I need a basic micro controller IC which can give me a 3-5 volts at its input/output pins.
and I want to know what is the easy way to learn how to interface LCD display and other peripherals to a micro controller?
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Dear Anusha, welcome, In this case, we have various type of micro-controllers, such as Arduino ( AVR base), LPC17xx ( ARM series).Arduino series are cheap. due to they have boot-loader they are easier than others.For Arduino series you can see link below:
Arduino Uno R3 is a good and cheap board. it's available it link below :
another board but smaller with Arduino Uno detail is Arduino nano or pro-mini, and they are available it blow links:
ARM series are reliable and they have been used in industrial projects. Best wishes.
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Can anyone Explain me how to connect two external button on 8 channel Open Brain computer interface system ( ADS1299) ? What is circuit diagram for Pin connection ? what is the code for interface ?
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Thank you Very much Joerg Fricke sir.
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Hi, when we use smartphone to capture a scene and display it on smatphone's screen, we got always color appearance difference between displayed and real objects. So I'm wondering how can we do on image processing pipeline and display pipeline to reduce it?
To lower the difficulty, we can suppose that the illumination condition is well known and device is iphone series like iphone6s or iphone 7plus (good color management). So I Know some techniques like Using raw data for large range imaging, Using color checker to calibrate camera, and anything else? 
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@Branko Livada thanks, I will check this out. 
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Should I hook them up in parallel? Do I need 3 volt controls and a combiner? This will be for off-grid use. 
Thank you.
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Thank you both very much for your excellent replies to my question! I am working on the schematic.
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I have heard we can use the phase and amplitude modulation of SLM to implement a lens on SLM. How should I do it, please provide some references. Thanks
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Dear Sahil,
in addition to the previous mentioned paper and lecture, you can add the following material:
-Akondi Vyas et al., "Spatial Light Modulator for wavefront correction", 2009.
-A Reflectance Display: Supplemental Appendix - Harvard University at vision.seas.harvard.edu/reflectance_display/SLM_appendix.pdf
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I haven't been following up the progress in this. 
First of all, I don't know transparent displays are based which of the existing technologies. Is it LCD? OLED, E-ink? or something else?
Let's assume transparent displays are based on LCDs, then we have to get rid of polarizers, color filters, back-lights. Although I know there is still another type of polarizers that might be critical for this type of application. To get rid of color filters, multiplexing in the time domain seems to me the only choice.
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Thank you, particularly Daniela, for pointing out the connection between transparent displays and Zeiss smart glasses. I'm still digesting all this. Semi-transparent films can be many types, not just amplitude- (or intensity-) divided. Polarization, spectrum, or even phase and diffraction orders might be exploited. Sophisticated wave-guide type of lights can be placed at the edges instead of blocking the view. So many possibilities. Janus particles, is that also a possibility? So my understanding is that Zeiss smart glasses are actually transparent near eye displays, and still a lot of work to be done to solving the problems of sever eye strains and people's having  a hard time focusing on the images on the glasses.
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we are trying to dissolve a crystal for liquid crystal display and would like to know which solvent to choose.
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As a rule of thumb, like matters dissolve each other. For example, polar liquids may dissolve polar materials.
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The TS-7800 implements a sleep mode that allows the board to go down to 200 micro amps. This power off the TS-7800 while the AVR waits for the specified time to wake up the board. It can make sleep for 5 seconds by running this:
root@ts7800:root# ts7800ctl -s 5 This only allows the board to sleep for seconds, not smaller units of time. It is however wake up immediately from an
external interface by driving DIO_04 or ISA_B32 high. This sleep functionality will only work if power is fed in through the +5V connector on the TS-7800 itself. If you are using a PC104 device like the TS-POE100 or the TS-BAT10 then you would have to cut the +5V pins on PC104 and bring it down to the TS-7800 power connector in order to use the sleep functionality. Otherwise the board can be powered through PC104 with no modification. 
The Display data has two sub-function “Line” and “Scroll”.
i) The Line sub-function reads a long characters string from a file as an input and convert into lines (for each 24
characters).
ii) The “Scroll” sub-function displays the input string and data onto the LCD display panel line by line, where the keypad plays to scroll lines up- down.
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Qasim,
LCD typically has a what's called "LCD module", which servers as the interface between a programmer and the LCD. In your case, if your LCD is directed controlled by this TS-7800 embedded /controller/microcomputer, you should be able to find a manual such as "TS-7800 databook" or something, in which you can find the function you are looking for. Otherwise, say if the LCD is controlled by a module mainly consisting of HD44780 (a very popular LCD controller), you should be able to find a manual for HD44780, and look for the code for the sleeping mode.
If the problem is that you don't understand the "code", I recommend you find a book on either embedded system or microcontroller/microcomputer (the easier to read the better), or ask someone who has a background in these things.
Good luck.
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Experiments using IP Core, LCD display, PWM generation, System generator, etc.,
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thank you for all your response
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I have LCD (from top way display model LM6059BCW) and i want to use it with microcontroller PIC16F877a. How can I redefined on MicroC software library?
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LM6059BCW based on ST7565P LCD-controller. On MicroC include ported-version of open-cource GLCD-library with low-level driver only one for Samsung KS108/KS107 LCD-controller. ST7565P and KS108/KS10 are not compatible. See https://www.mikroe.com/forum/viewtopic.php?f=72&t=56735  
You can use vanilla GLCD-library and self-port driver code for ST7565P by example for KS108/107 from MicroE --> http://www.mikroe.com/download/eng/documents/compilers/mikroc/pro/pic/help/graphic_lcd_library.htm
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I'm looking for firmware that can update sim900 A for working with DTMFs and also programming sim900 A to connect a LCD and keypad to it.(without using micro controller)
any ideas???
Best regrets
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Hello Vahid,
Although you have the firmware as open source, is it having the details of the hardware? If the hardware was also open source like the Arduino platform, it would have been much easier for you. That is why I stated as to do some HACKING into the hardware - do some R & D (read as Repairs and Damages) on the board!
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I've put the LCD initialization code in CodeVision in different parts of the initialization segment of the program and it only works in certain places , one of which is where the Wizard uses as default.
Is there any explanation why such sequence occurs, or how to put the initializer code for any part in the right place without checking the Wizard?
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Yes, in one of my application if i initialise timer2 after timer0 it interrupt does not work. My code is right. Company people will not tell you this thing. I have even found fault in microchip devices datasheet
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When power supply conducts like Transistor, inductor, capacitor and other side diode like OLED, LED, LCD
here in resisitor purpose of resists the current  and inductor , capacitor same as we know the purpose
In other side  while LED omits the lights, so here the used Photovoltaic principle
In reisitance under the ohms law.
My doubts or questions if any other principle is there? and what is the basic think in material science?
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It is band theory that tells whether the material is conductor, insulator or semiconductor
If band gap very high such material behave as insulator. If band gap (energy difference between lower edge of conduction band and upper edge of valance band) is small ( may be 0.5 eV to several eV need to confirm from book) then it behave as semiconductor. If band is half filled such material behave as metallic behavior. You can find detail information in general Solid State Physics book
If the band gap of material in the range of energy of visible light, such material show photovoltaic effect and can be used to fabricate solar cell.
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Hi,
I am trying to mechanically rub BCB polymer films (the polymer derived from B-staged bisbenzocyclobutene) to introduce some fine grooves (~50 nm wide) on its surface. I found that people in LCD manufacturing use a piece of cloth (described as velvet, microfiber or velour cloth) for rubbing (attached paper).
I do not know where to buy this type of cloth. I tried to use the one similar to this the one on the amazon link but the grooves are not homogeneously distributed on the surface.
I would really appreciate it if anyone could provide me with some useful information to find the right cloth.
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That type of material should be effective and is typically available at a fabric store. Back in the 1980s we used polyester - I don't know what people are using thes days.  A smooth polyester paint roller was very effective.  In my research, I found that the rubbing causes the polymer molcues at the surface to realign in one direction and it is the intermolecular (van der Walls) forces that cause the LC molecules to align in the direction of the orientation of the polymer moleules.  We never saw any grooves.  See my paper entitled "Surface Anchoring of Liquid Crystal Molecule on Various Substrates" on the Research Gate website.  
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I would like to calculate the delay between image captured by camera and same image displayed on LCD display. So time required to display the frame captured by camera on LCD display. Normally this delay value lies in between 100 to 200ms. But I want to calculate more appropriate value.
For now, I am flashing LED light in front of the camera and this is getting displayed on LCD. I have placed one Photodiode in front of LCD display to detect the flashing light.
My idea is to see the square waveform at LED and the delayed waveform at Photodiode after detection of flashing light.
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A processor (within the camera) can be made to start counting while camera is flashing and the timer can be made into off when the signal reaches the LCD.
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What else i can interface arduino with MATLAB.?
I have interfaced LCD, LED and Motor.
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Use the ArduinoIO from http://www.mathworks.com/matlabcentral/fileexchange/47057-arduinoio-zip, it is essentially a gateway host inside the arduino with MATLAB support object that traffics common arduino commands via MATLAB
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  1. Can you program it using micro controller or FPGA?
  2. Can you light up all pixels in an LCD in the same time?
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If you know the input voltage standard of the image sensor, then you can adjust the FPGA output voltage standard through the programming software to match the sensor voltage.
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I need your help to set up the electrophysiology system. I am getting heavy background when I focus the acute slice on screen. I mean, it is difficult to view the neuron brightly. There is LCD monitor with the rig. Can anyone suggest me where may have problem or what should I do to improve the brightness of neurons? Please help me if you can. Thanks, Shahid
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For any optics you have: check the lens of your immersion objective. Carbonate accumulates periodically in a film on top of the lens and reduces the visibility. You might need to rub it off. Check the allignment of your condensor (look online "Kohler illumination to learn how to do it).
If you do NOT have DIC-infrared optics, check the visibility of neurons from young animals: in mice before P12 the myelination is not yet complete and brain slices look transparent. You should see the somas (anywhere in the brain) well outlined. With aging and myelination you will greatly loose visibility. In adult, without DIC optics the cell somas are not visible (you should ask your boss to buy you DIC optics if you work on adult animals... it will save you years of work).
If you do have DIC-infrared optics: Rotate the polarized-lens filter to optimize the contrast of cell somas.
Also
Check that the recording chamber is clean (glas surface free from carbonate concretions). If not, scrub it (lightly acid solution helps) or replace the glass bottom.
Check the contrast settings of you imaging program... but I guess you did that already. Same of course for the light source intensity...
Good luck!