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Reference channel

Fig. 1 shows the block diagram of the vibrometer, in which the most sensible to small phase variations interferometric scheme is employed. It consists of the microwave and the display units. The display unit consists of the power supply 1, controller 2 of the phase modulator 3, microprocessor unit 9 and low-frequency amplifier 10. The microwave unit contains the electromechanical phase modulator 3, a solid-state microwave oscillator 4, an attenuator 5, a bidirectional coupler 6, a horn antenna 7 and a microwave detector 11. The horn antenna is used for transmitting the microwave and receiving the reflected signal, which is mixed with the reference signal in the bidirectional coupler. In the reference channel the electromechanical phase modulator is used to provide automatic calibration of the instrument. To adjust the antenna beam to the object under test, the microwave unit is placed on the platform which can be shifted in vertical and horizontal planes. [Pg.655]

Fig. 3.15 Left External view of the MIMOS II sensor head (SH) with pyramid structure and contact ring assembly In front of the Instrument detector system. The diameter of the one Euro coin is 23 mm the outer diameter of the contact-ring is 30 mm, the inner diameter is 16 mm defining the field of view of the Instrument. Right. Mimos II SH (without contact plate assembly) with dust cover taken off to show the SH Interior. At the front, the end of the cylindrical collimator (with 4.5 mm diameter bore hole) Is surrounded by the four SI-PIN detectors that detect the radiation re-emltted by the sample. The metal case of the upper detector is opened to show its associated electronics. The electronics for all four detectors Is the same. The Mossbauer drive is inside (in the center) of this arrangement (see also Fig. 3.16), and the reference channel is located on the back side In the metal box shown In the photograph... Fig. 3.15 Left External view of the MIMOS II sensor head (SH) with pyramid structure and contact ring assembly In front of the Instrument detector system. The diameter of the one Euro coin is 23 mm the outer diameter of the contact-ring is 30 mm, the inner diameter is 16 mm defining the field of view of the Instrument. Right. Mimos II SH (without contact plate assembly) with dust cover taken off to show the SH Interior. At the front, the end of the cylindrical collimator (with 4.5 mm diameter bore hole) Is surrounded by the four SI-PIN detectors that detect the radiation re-emltted by the sample. The metal case of the upper detector is opened to show its associated electronics. The electronics for all four detectors Is the same. The Mossbauer drive is inside (in the center) of this arrangement (see also Fig. 3.16), and the reference channel is located on the back side In the metal box shown In the photograph...
Fig. 3.19 Schematic illustration of the measurement geometry for Mossbauer spectrometers. In transmission geometry, the absorber (sample) is between the nuclear source of 14.4 keV y-rays (normally Co/Rh) and the detector. The peaks are negative features and the absorber should be thin with respect to absorption of the y-rays to minimize nonlinear effects. In emission (backscatter) Mossbauer spectroscopy, the radiation source and detector are on the same side of the sample. The peaks are positive features, corresponding to recoilless emission of 14.4 keV y-rays and conversion X-rays and electrons. For both measurement geometries Mossbauer spectra are counts per channel as a function of the Doppler velocity (normally in units of mm s relative to the mid-point of the spectrum of a-Fe in the case of Fe Mossbauer spectroscopy). MIMOS II operates in backscattering geometry circle), but the internal reference channel works in transmission mode... Fig. 3.19 Schematic illustration of the measurement geometry for Mossbauer spectrometers. In transmission geometry, the absorber (sample) is between the nuclear source of 14.4 keV y-rays (normally Co/Rh) and the detector. The peaks are negative features and the absorber should be thin with respect to absorption of the y-rays to minimize nonlinear effects. In emission (backscatter) Mossbauer spectroscopy, the radiation source and detector are on the same side of the sample. The peaks are positive features, corresponding to recoilless emission of 14.4 keV y-rays and conversion X-rays and electrons. For both measurement geometries Mossbauer spectra are counts per channel as a function of the Doppler velocity (normally in units of mm s relative to the mid-point of the spectrum of a-Fe in the case of Fe Mossbauer spectroscopy). MIMOS II operates in backscattering geometry circle), but the internal reference channel works in transmission mode...
The primary method for velocity cahbration is the internal reference channel with reference target and detector configured in transmission geometry (Fig. 3.16). [Pg.66]

Fluorescence spectra were recorded using an SLM 4800 spectrofluorimeter (Bioritech, Chamarande, France) fitted with a thermostat-controlled (30°C) front-surface accessory. The incidence angle of the excitation radiation was 60°. Coagulation kinetics were performed in a quartz cuvette 1 cm x 1cm. All spectra were corrected for instrumental distortions in excitation using a rhodamine cell in the reference channel. [Pg.283]

The solution to 5 decimal places is 0.10886..., or 10.886 %T. The solution given by Ingle and Crouch for this case, which again, does not take into account the variation of the reference channel is 13.5%T ([10], p. 153). [Pg.297]

We therefore see that in this case also, neglecting the reference channel error also causes a noticeable change in the answer from the correct one. [Pg.298]

In Figure 52-30 we plot the function -1 /ln(T) to complete this part of the analysis. We note that there is no minimum to the curve, and the noise from source continually improves as the transmittance decreases in this case the previous, conventional derivations agree with our results, although they do not indicate the V2 factor. Noting the transitions from equation 52-140 to 52-142 (and the corresponding portions of the derivation for absorbance noise and relative absorbance noise), we see that this factor arises from the equal noise contributions of the sample and reference channels therefore we conclude that in this case also, the missing factor is due to the neglect of the reference channel noise contribution. [Pg.326]

If one chooses channel i,i= 1,2N — 1, to be the measuring channels, and channel N as a reference channel, where N is the total number of the channels, the refractive index changes A/Verf llV may be determined using (10.6) by measuring the spatial shifts AyiN. Section 10.2.3 demonstrates that this approach allows determining either the amount of adsorbed analytes on the sensor surface, or alternatively the change in concentration of analytes in the bulk solution. [Pg.272]

If channels 1, 2, and 3 are chosen as measuring channels and channel 4 as a reference channel, it will be possible in principle to monitor independently and simultaneously three different binding events, each of them taking place in one of the measuring channels. [Pg.273]

To give an example both sensitivity coefficients are evaluated for the current sensor (see Sect. 10.3 for details). For the bulk detection of glucose this results in A bulk (rad) = 5.6 x 102 AC (g/ml), whereas for the adsorption of proteins on the sensor surface the overall sensitivity of the sensor is evaluated as A< >layer (rad) = 2.0 x 10 5 Am/A (fg/mm2). Measuring the phase change A< >,-, between any of the two channels i and j can thus give an estimation on the change in analyte concentrations between those two channels. If one channel (e.g., channel N) is used as a reference channel, then ACV = 0 and AmN = 0 and absolute analyte concentrations can be determined. [Pg.275]

The performance of the realized YI sensor was first tested by applying solutions of different concentrations of glucose in water, thus inducing well-defined refractive index changes between measuring and reference channels of the device. In... [Pg.279]

The possibility to use the YI sensor for virus detection was explored by monitoring the interaction between a-HSV-1 gG antibody and HSV-1 virus particles. To this end, channel 1 was coated with protein pA as described in Sect. 10.4.2 followed by the immobilization of a a-HSV-1 gG layer on the sensing surface of channel 1. Channel 4 was used as a reference channel. Finally a solution with HSV-1 virus particles at a concentration of 105 particles/ml was added to channel 1. Figure 10.2 shows the phase change measured between channel 1 and reference channel 4, clearly demonstrating the detection of virus particles by the YI sensor (Fig. 10.15). [Pg.287]

Fig. 10.15 Virus detection test. Sensor signal (phase change) measured between channel 1 and the reference channel for the immobilization of anti HSV 1 glycoprotein G monoclonal antibody layer on the sensing surface of channel 1 (A HSV i gG) and the binding of HSV 1 particles to this layer (A IISV i). Reprinted from Ref. 28 with permission. 2008 American Chemical Society... Fig. 10.15 Virus detection test. Sensor signal (phase change) measured between channel 1 and the reference channel for the immobilization of anti HSV 1 glycoprotein G monoclonal antibody layer on the sensing surface of channel 1 (A HSV i gG) and the binding of HSV 1 particles to this layer (A IISV i). Reprinted from Ref. 28 with permission. 2008 American Chemical Society...
Fig. 10.17 Specific detection of HSV 1. Phase changes A Fig. 10.17 Specific detection of HSV 1. Phase changes A<P14 and A 24 in the four channel YI sensor as a function of time during several processes. HSA solution was first flowed through channels 1 and 2 simultaneously (Al and A2). Next, after washing with PBS, HSV 1 solution was flowed in channels 1 and 2 simultaneously (B1 and B2) PBS was continuously flowed in reference channel 4. Thus, the four graphs show the following interactions (Al) a HSA HSA, (A2) a HSV 1 gG HSA, (Bl) a HSA HSV 1, (B2) a HSV 1 gG HSV 1. Note that initial phases in Al and A2 were shifted to 0 for clarity. Reprinted from Ref. 28 with permission. 2008 American Chemical Society...
This detector responds to infrared emissions in at least two wavelengths. Typically a CO2 reference at 4.45 microns is established and a second reference channel that is away from the CO2 and H2O wavelengths is made. It requires that the two signals received are confirmed as are synchronous and that the ratio between both signals is correct. [Pg.181]

A reference channel (quantum counter or photodiode) has two advantages (i) it compensates for the time fluctuations of the lamp via a ratiometric measurement (ratio of the output signals of the photomultiplier detecting the fluorescence of the sample to the output signal of the reference detector) (ii) it permits correction of excitation spectra (see below). [Pg.157]

K. T. V. Grattan, R. K. Selli, and A. W. Palmer, Fiber-optic absorption temperature sensor using fluorescence reference channel, Rev. Sci. Instrum. 57, 1175-1178 (1986). [Pg.294]

The detector will observe negative peaks. Most instruments can cope with negative peaks by reversing the signal (Eigure 4) or subtracting a reference channel so that the peaks appear as positive or at least are integrated as positive peaks. [Pg.322]

The detection limit is generally limited by electronic and mechanical noise, thermal drift, light source instabilities and chemical noise. But the intrinsic reference channel of the interferometric devices offers the possibility of reducing common mode effects like temperature drifts and non-specific adsorptions. Detection limit of 10 in refractive index (or better) can be achieved with these devices which opens the possibility of development of highly sensitive devices, for example, for in-situ chemical and biologically harmful agent detection. [Pg.132]

Figure 2. Heat conduction (Seebeck effect) batch mixing calorimeter for three samples and one reference channel. After loading and establishing baselines, the assembly is inverted to mix reactants and start heat production. (Reproduced with permission from Ref. 2. 1983, Alan R. Liss, Inc.)... Figure 2. Heat conduction (Seebeck effect) batch mixing calorimeter for three samples and one reference channel. After loading and establishing baselines, the assembly is inverted to mix reactants and start heat production. (Reproduced with permission from Ref. 2. 1983, Alan R. Liss, Inc.)...
Smaller values of are obtained for interferometers operated in a double-beam mode, since the moveable mirror must be left stationary for a fraction of the cycle time to allow the detector to stabilize each time the beam is switched from the sample to the reference position. With an optical null grating spectrometer the chopper is used not only to modulate the beam but also to alternate the beam between sample and reference channels. Thus, it takes approximately the same time to measure a transmittance spectrum using a double beam optical null spectrometer as it takes to measure a single-beam spectrum with the same S/R. Hence, for this type of spectrometer may be assigned a value of 2. [Pg.23]

At the end of the 3 sec averaging period the signal on the reference detector D2 is checked. If the reference channel indicates that the line is not exactly at the center of the 128 step ramp the computer adjusts the laser temperature to bring the line back to the center. [Pg.274]


See other pages where Reference channel is mentioned: [Pg.655]    [Pg.241]    [Pg.270]    [Pg.273]    [Pg.50]    [Pg.149]    [Pg.235]    [Pg.240]    [Pg.158]    [Pg.13]    [Pg.110]    [Pg.86]    [Pg.167]    [Pg.44]    [Pg.46]    [Pg.151]    [Pg.151]    [Pg.241]    [Pg.156]    [Pg.173]    [Pg.224]    [Pg.44]    [Pg.46]    [Pg.102]    [Pg.346]    [Pg.147]    [Pg.506]    [Pg.124]   
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