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Ni usb 6353

Manufactured by National Instruments
Sourced in United States

The NI USB-6353 is a high-performance multifunction data acquisition (DAQ) device that provides analog input, analog output, digital I/O, and counter/timer functionality. It offers 16-bit resolution, sampling rates up to 1 MS/s, and multiple connectivity options for a wide range of laboratory and test applications.

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3 protocols using ni usb 6353

1

Electrical Impedance Tomography DAQ Protocol

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A 16 bits DAQ board is connected to the circuit (National Instruments NI-USB 6353); the DAQ has been set to acquire, at rate 1 MSa/s, a number of 3000 samples (corresponding to 300 periods of the driving voltage) of each differential voltage ui=ViV0 , where Vi is the potential of each electrode surface Si and V0 is the potential of the lower electrode, chosen as reference, Figure 2a. The current signal I flowing through the outer electrodes is acquired as a single ended trace referred to ground. A dedicated control panel, shown in Figure 3, developed in LabView, acquires the data of the driving current and of ui . During a measurement cycle, the DAQ reads the nine differential voltages ( ui ) and the current signal (I). The measurement time for each channel is 3 ms, thus the acquisition time is 30 ms. After acquisition, the control panel calculates the AC-coupled RMS value of each quantity and saves the results into a text file. The volume of the defects is then computed with a Matlab script which calculates the quantity ΔR(D) as described in the next subsection.
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2

Voltage Transient Measurements for Electrodes

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The voltage transient measurements using a charge-balanced biphasic current-controlled waveform were performed with an analog stimulus isolator (AM 2200, AM Systems, Sequim, WA, USA). A bespoke MATLAB program (R2016a, Mathworks, Natick, MA, USA) was used to generate stimulating waveform with specific pulse width, amplitude, and frequency. The pulses were injected into the electrode-electrolyte test cell, and a data acquisition board (NI USB-6353, National Instruments, Austin, TX, USA) was used to record the voltage transient responses. The charge-balanced biphasic pulse used in the experiments were cathodic-first current pulse with 100 μs duration followed by 100 μs inter-phase delay. The stimulating frequency was set at 50 Hz. The maximum negative potential excursion (Emc) was esteimated to be the potential immediately after the end of the cathodic pulse (Fig. 5A). The time delay at which the current becomes zero was measured to be approxmiately 12 μs, and Emc was recorded at 12 μs following the end of the cathodic current pulse. Vdr is the negative driving voltage which is maximum voltage to deliver the cathodic current pulse.
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3

Subsurface Optical Imaging of Tissues

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A glass container with 1 cm lateral dimension was filled with PbS QD chloroform solution and was submerged in the liquid phantom solution or biological tissues at a depth z below the air/ solution or air/tissue interface. Bovine liver tissues and porcine skin tissues were obtained from the local butchers, and the thicknesses were measured by Vernier calipers. The light source emitting 915 nm laser (Changchun New Industries, FC-W-915) has an incidence angle of 30 deg with respect to the detector that is perpendicular to the air/tissue interface. Light intensity was measured with a digital optical power meter (Thorlabs, PM100). An InGaAs CCD camera (FLIR, SC2500-NIR) was used for the SOW imaging. A 1000 nm long-pass filter (Thorlabs, FEL1000) and a zoom lens (Navitar, 1-60135-IR) were attached in front of the CCD camera. The working distance between the samples and the zoom lens was ∼40 cm and the field of view was 5 × 5 cm 2 . The light source and InGaAs CCD camera were synchronized with a trigger signal using a data acquisition board (National Instruments, NI USB-6353).
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