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SCR - Science topic
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Questions related to SCR
Chemical reaction of exhaust gas in SCR is
4NH3+4NO+O2---> 4N2+6H2O.
What is rate of reaction for this ?
Chronic Kidney Disease (CKD) is a global public health concern characterized by gradual kidney function loss. CKD management requires medical intervention and patient involvement in Self-Care Regimens (SCR) and Health-Promoting Behaviors (HPB). SCR involves actions like medication adherence, dietary restrictions, and lifestyle changes that control disease progression and enhance patient well-being.
However, adherence to SCR can be challenging due to psychological factors and individual traits. Emotional Intelligence (EQ), the ability to recognize, understand, manage, and express emotions effectively, is increasingly recognized for influencing health behaviors. EQ might mediate the CKD-SCR-HPB relationship.
Though EQ's impact on health is explored, its mediating role in CKD patients' SCR and HPB engagement remains underexplored. This study addresses this gap, informing interventions tailored to CKD patients' emotional needs. If EQ mediates SCR-HPB engagement, interventions targeting EQ could enhance coping, improving adherence and health outcomes.
This research delves into EQ-SCR-HPB interplay in CKD patients, contributing to healthcare strategies for better CKD management.
I need articles for poisoning effect of heavy metals on Ce- based SCR catalysts
Hi all,
Our research group is currently working on the development of a wireless wristband for monitoring EDA. We chose the dorsal side of the left distal forearm as our recording site (where right-handed people usually wear their watches), and we chose to use oval-shaped stainless steel electrodes for our recordings. ADI Company's sensor chip was applied. Several problems were raised when evaluating the performance of our device regarding its sensitivity and accuracy.
We used sad movie clips to induce emotional arousal in participants while monitoring GSR changes. Those clips were found to successfully arouse desired emotional responses during the experimental processes. We then compared the performance of our wristband with the Empatica E4 wristband in terms of their consistency in measuring SCL and SCR components. We also compared our device with the Shimmer GSR sensor (which collected GSR at distal sites of the fingers) to compare their measures during emotional arousal and to further evaluate our device's sensitivity and accuracy.
Our results showed that, overall, our wristband performed worse than the E4 wristband, mainly indicated by differences in amplitudes of SCLs as well as the frequency and amplitude of SCRs. For example, when compared with neutral movie clips, although sad movie clips induced some emotional response, GSR trends recorded using our device were not as significant as those recorded by the E4 and the Shimmer devices. A very low proportion of SCRs recorded using our device exceeded the 0.05μS threshold, while the E4 wristband captured much more significant SCRs. Moreover, it takes a relatively long time for our wristband to get stabilized signals compared to E4 after our participants put on them.
Since the E4 wristband and the Shimmer sensor use the inner wrist and fingertips respectively as their recording sites, and both of them use Ag/AgCl electrodes, we speculate the recording site and the type of electrodes to be the most important reasons for inconsistencies found between our device and these two standardised devices. We have also considered the influences of environmental temperature and humidity, but given that our experiments were conducted within a constant environment, these influences should have been counterbalanced. Therefore, we've got four questions here:
1. Is the dorsal side of the distal forearm a viable site for recording GSR?
2. Are stainless steel electrodes capable of capturing endogenous, relatively weak physiological changes?
3. A minimum of 0.05μS is typically set as a threshold to define significant SCR. However, in our case where the GSR signal fluctuated in a relatively stable manner, can we set our threshold at a lower level, 0.01 μS for example?
4. Any advice on shortening the time the wristband takes to get stabilized signals?
Thanks for your time. Any advice on these queries would be greatly appreciated!
Through years operation, some of the devices' pins connection gradually become worse and finally burn out due to the high temperature at the connection point. We can check out these risk points via IR scan method. I am trying to have a total solution.
Hi,
I am looking for a suitable method to take into account the non specific SCRs when computing the average SCL.
Since non specific SCRs artificially distort the SCL, I want to "remove" them from my SCL.
I compute average SCL on 1 min periods. Should I compute the mean of all the SCRs amplitude within this 1 minute and substract it from the average SCL ?
Thank you in advance.
The world is trying hard to switch into Electric Vehicles right now and not many research units are focusing on IC Engines anymore. At the present scenario, is there any known Post-doc position vacancy likely to be applied for, in Engines field.??
Kindly do Share your expertise in this.
Thank You.
Though AVE value must be greater than 0.5, yet the question is can i go ahead with further calculations if AVE is close to 0.5. (Little less than 0.5)...All other values, like factor loading, SCR, data adequacy etc is coming under the acceptance zone?
Imagine a SCR survey where the target species was not detected by a single camera-trap. The sampling effort was similar to the one of successful SCR surveys in other regions. Given the sampling effort, how sure can you be that the species was not in the study area? or how confident are we that indeed not a single individual was present in the study area during the survey? Do you know a paper on this subject and/or an approach that enables to estimate if the sampling effort was enough? Many thanks
I need to convert the normal household microwave into a research one with controllable output power. I thought if i varied the voltage supplied to the magnetron, i can control its power. But i need a definitive answer before i start working based on this theory.
It is very interesting to know the formation of N2O in the combustion chamber. The formation of NOx takes place through 3 ways and one being the most common, that is the thermal method, other two being the formation of NOx through Nitrogen oxidation through HC's and last one through the intermediate step called the N2O method.
Now the question is what happens if the N2O is not fully converted to NOx ?
When will the NOx be formed through N2O method ?
How to avoid this route for NOx formation ?
#Nitrous Oxide, #Diesel Combustion, # SCR,, # Catalyst , # NOx
How much can we further reduce the amount of NOx in the exhaust by uing a SCR (with urea) ?
The NOx concentration level is higher in DPP as they didn’t install any NOx control methods. We suggested using Selective Catalytic Reduction (SCR) method for controlling NOx emission. Ammonia (NH3) is making use of reagent in SCR technique and it is inject to the exhaust stream
I want to calculate the SMD for UREA SCR spray at 5 bar injection pressure .
Dear People,
I have data, recorded by a set of 12 cameras in a 5x5km grid, with 1 camera position in each cell for every month (July-December, 4 positions in total/per grid cell). These positions are spatially dependent because of the small grid size and greater homerange size of the target species: Ursus arctos.
My question is, if I can conduct a single season occupancy model for that kind of data, although a requirement seems to be spatially independent sample sites,
or if I should use spatial capture-recapture models (SCR) to analyse habitat selection and spatial behaviour instead?
Another question is: how many trap days should be considered as one repeated visit (occasion- K) for the occupancy model? (3-7?)
Last but not least: does anybody know, where to get daily temperature and precipitation data for Greece :)?
Thank you so much
I have deigned phase angle control block using TCA 785 . I want to design feedback control for controlling current through SIngle phase SCR based rectifer. Also I need guidance to realise circuit for PID controller. Any help in this relation would be highly appreciated.
In SCR technique, to control NOx emission generally ammonia is sprayed. Any other chemical available instead of ammonia.
I have to discharge some kiloamps from a capacitor through an inductor by using two SCRs or thyristors in triac configuration, but I should need to be sure maximum dv/dt and di/dt current is not reached, so what of following configurations are better?

What is selective catalytic reduction (SCR) method for NO* control in gas turbines ?
Normally in adapter application power supply diode rectifier are used, by using SCR's instead of diodes we can eliminate PWM controller
What will happen if its value is large or small?
Recently I'm using CASSCF to calculate spin orbit cooupling on ethylene as a test sample. Input is showed below:
#p casscf(4,4,spinorbit)/LANL2DZ scfcon=5 scfcyc=900 scf=direct
test nosym guess=read geom=check SP
However, Error I510.exe happened.
Len28= 115739 LenMCI= 42354.
Leave Link 405 at Fri Oct 21 16:23:09 2016, MaxMem= 3276800000 cpu: 29.1
(Enter /pkg/chem/gaussian/g09/l510.exe)
Enter MCSCF program.
NO. OF ORBITALS = 26 NO. OF CORE-ORBITALS = 6
NO. OF VALENCE-ORBITALS = 6 NO. OF VIRTUAL-ORBITALS = 14
USED ACCURACY IN CHECKING CONVERGENCE = 1.00D-04
Blank line reading weights.
Error termination via Lnk1e in /pkg/chem/gaussian/g09/l510.exe at Fri Oct 21 16:23:31 2016.
Job cpu time: 0 days 0 hours 0 minutes 52.1 seconds.
File lengths (MBytes): RWF= 5 Int= 0 D2E= 0 Chk= 1 Scr= 1
Error: segmentation violation
rax 0000000000000000, rbx ffffffffffffffff, rcx ffffffffffffffff
rdx 000000000000802c, rsp 00007fffdaf69418, rbp 00007fffdaf69990
rsi 000000000000000b, rdi 000000000000802c, r8 00002adb9bbee2c0
r9 0000000000000000, r10 00007fffdaf691a0, r11 0000000000000206
r12 0000000000000000, r13 0000000000000000, r14 00007fffdaf699d8
r15 00000000000003e6
/lib64/libpthread.so.0(+0xf130) [0x2adb9bdef130]
/lib64/libc.so.6(kill+0x7) [0x2adb9c3338a7]
/pkg/chem/gaussian/g09/l510.exe() [0x7a3549]
/pkg/chem/gaussian/g09/l510.exe() [0x7ae651]
/pkg/chem/gaussian/g09/l510.exe() [0x7eac2d]
/pkg/chem/gaussian/g09/l510.exe() [0x7db955]
/pkg/chem/gaussian/g09/l510.exe() [0x433e52]
/pkg/chem/gaussian/g09/l510.exe() [0x4178ba]
/pkg/chem/gaussian/g09/l510.exe() [0x403f4c]
/pkg/chem/gaussian/g09/l510.exe() [0x403370]
/pkg/chem/gaussian/g09/l510.exe() [0x4032ad]
/lib64/libc.so.6(__libc_start_main+0xf5) [0x2adb9c31faf5]
/pkg/chem/gaussian/g09/l510.exe() [0x4031a9]
I have read Gaussian manual and the closest question I can find on Researchgate.
I still can't figure out how to solve this kind of problem. Could some kindly help me out.
I would like to use skin conductance responses to indicate when a participant has seen something that is very salient to them and grabs their attention during unconstrained viewing of real, natural stimuli. This would involve using eye-tracking in combination with measuring SCR, and seeing what the participant was looking at when a SCR was evoked. However I am new to the SCR method and am not sure if this approach is feasible or is valid from a theoretical standpoint. Any advice or links to relevant papers would be greatly appreciated.
Thanks,
Jim Uttley
In case of connecting a Wind farm to a weak grid with short circuit ratio (SCR) less than 3. What are the procedures that must be done?
What are the main analytical results from Dilatometric Thermal Analysis?
spent SCR catalyst
Does anyone can guide about Euro V & SCR system capability?
Are there any cheap NOx reduction methods to reduce NOx emissions from IC engines. As SCR methods are costly and consume more fuel to have after burning in the exhaust port.
Can I use 555 timer to trigger SCR / MOSFET for Boost Converter Applications?
I'm thinking about SCR, EEG, fMRI, eye scanning, etc... indices that would indicate inattention during reading, driving etc ... References to relevant literature would be appreciated. Tx
Hi all,
I find the use of the word 'restart' with respect to the Gaussian documentation to be a little vague. I have performed an IRC calculation (reverse) for 20 steps without reaching a minimum (the product). I suspect I am only a few steps away. How do I 'continue' for an additional 20 steps?
Using GView I tried:
%chk=IRC_1_1_rev.chk
# irc=(restart,reverse,maxpoints=40,recalc=5,calcfc) rwb97xd/6-31+g(d) scrf=check guess=tcheck geom=(allcheck) genchk
But this results in the following error:
IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC-IRC
Restoring state from the checkpoint file "IRC_1_1_rev.chk".
Title: Title Card Required
Route: # irc=(reverse,maxpoints=20,recalc=5,calcfc) rwb97xd/6-31+g(d) scrf=chec
k guess=tcheck geom=(allcheck) genchk
------------------------------------------------------------------------
INPUT DATA FOR L123
------------------------------------------------------------------------
GENERAL PARAMETERS:
Rxn path following direction = Reverse
Maximum points per path = 40
Step size = 0.116 sqrt(amu)*bohr
Integration scheme = HPC
Redo corrector integration= Yes
DWI Weight Power = 2
DWI will use Hessian update vectors when possible.
Max correction cycles = 20
Initial Hessian = CalcFC
Hessian evaluation = Every 5 predictor steps
Hessian updating method = Bofill
------------------------------------------------------------------------
RESTARTING THE IRC JOB
Error in corrector energy = -0.0000357145
Magnitude of corrector gradient = 0.0279347254
Magnitude of analytic gradient = 0.0259326303
Magnitude of difference = 0.0038401131
Angle between gradients (degrees)= 6.9801
NTrRo=3 is not 5 or 6.
Error termination via Lnk1e in /shared/ucl/apps/Gaussian/G09_C01_L/g09/l123.exe at Sun Jul 26 18:15:35 2015.
Job cpu time: 0 days 0 hours 0 minutes 0.2 seconds.
File lengths
Notice how the route section in the input file (top of this message) is different to the log file, as though they input file route section has been completely ignore.
(MBytes): RWF= 30 Int= 0 D2E= 0 Chk= 38 Scr= 1
Any ideas?
Thanks
Hey I'm trying to run GLM and DCM models to analyze skin conductance data using SCRalyze from data output from BioTrace+, however I am a beginner with MATLAB and my computer science knowledge is limited.<br /><br />
Does anyone know or can anyone provide an easy explanation on how to run and view these results? Any help would be appreciated! Thank you!
This system should be compatible with SCR monitoring of the pain responses, only low level of pain induction is required.
Can someone also provide the terminal considerations in the anti-parallel configuration, if such a design is practically possible.
Can SCR can be turned on at zero degree firing angle?
I collected EDA data during sessions of the Iowa Gambling Task (IGT). I decided to compute skin conductance responses (SCRs) by simply measuring the absolute difference between onset and the maximum point within a 4-second window for each IGT event. I decided against computing for local baseline since trials were close to each other in time and prior SCRs would confound with a baseline computation. Am I right to do it this way?