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Filament conductivity

Thermal Conductivity Detector One of the earliest gas chromatography detectors, which is still widely used, is based on the mobile phase s thermal conductivity (Figure 12.21). As the mobile phase exits the column, it passes over a tungsten-rhenium wire filament. The filament s electrical resistance depends on its temperature, which, in turn, depends on the thermal conductivity of the mobile phase. Because of its high thermal conductivity, helium is the mobile phase of choice when using a thermal conductivity detector (TCD). [Pg.569]

When a solute elutes from the column, the thermal conductivity of the mobile phase decreases and the temperature of the wire filament, and thus its resistance, increases. A reference cell, through which only the mobile phase passes, corrects for any time-dependent variations in flow rate, pressure, or electrical power, ah of which may lead to a change in the filament s resistance. [Pg.569]

Process. Any standard precursor material can be used, but the preferred material is wet spun Courtaulds special acrylic fiber (SAF), oxidized by RK Carbon Fibers Co. to form 6K Panox B oxidized polyacrylonitrile (PAN) fiber (OPF). This OPF is treated ia a nitrogen atmosphere at 450—750°C, preferably 525—595°C, to give fibers having between 69—70% C, 19% N density less than 2.5 g/mL and a specific resistivity under 10 ° ohm-cm. If crimp is desired, the fibers are first knit iato a sock before heat treating and then de-knit. Controlled carbonization of precursor filaments results ia a linear Dow fiber (LDF), whereas controlled carbonization of knit precursor fibers results ia a curly carbonaceous fiber (EDF). At higher carbonizing temperatures of 1000—1400°C the fibers become electrically conductive (22). [Pg.69]

Bicomponent technology has been used to introduce functional and novelty effects other than stretch to nylon fibers. For instance, antistatic yams are made by spinning a conductive carbon-black polymer dispersion as a core with a sheath of nylon (188) and as a side-by-side configuration (189). At 0.1—1.0% implants, these conductive filaments give durable static resistance to nylon carpets without interfering with dye coloration. Conductive materials such as carbon black or metals as a sheath around a core of nylon interfere with color, especially light shades. [Pg.258]

Quantitative Relationship of Conductivity and Antistatic Action. Assuming that an antistatic finish forms a continuous layer, the conductance it contributes to the fiber is proportional to the volume or weight and specific conductance of the finish. As long as the assumption of continuity is fulfilled it does not matter whether the finish surrounds fine or coarse fibers. Assuming a cylindrical filament of length 1 cm and radius r, denoting the thickness of the finish layer as Ar and the specific conductance of the finish k, the conductance R of the finish layer is given by the equation (84) ... [Pg.292]

The specific conductance of the finish on the filament k is not necessarily the specific conductance it exhibits in its bulk condition. For instance, absorption of ions from the finish by the fiber can reduce the conductivity. The specific conductance greatiy depends on the amount of moisture present. Figure 4a shows the experimentally observed resistance of yam as a function of the amount of antistatic agent appHed in comparison to the calculated resistance. Below 0.05% of antistatic agent the experimental values show a lower conductivity than calculated this may be due to a lack of continuity of the antistatic agent. [Pg.292]

Electrical Hazards. Because carbon fibers are conductive, the airborne filaments can create serious problems shorting out electrical equipment. The best option is to locate sensitive equipment in clean rooms outside of areas where carbon fiber is being processed. If this is not possible, electrical cabinets must be effectively sealed to prevent contact with carbon fibers. A filtered air-positive purge provides additional protection for sensitive equipment. [Pg.7]

With the rotary and diffusion pumps in tandem, aided by a liquid-nitrogen trap, a vacuum of 10 Torr became readily attainable between the wars by degrees, as oils and vacuum greases improved, this was inched up towards 10 Torr (a hundred-billionth of atmospheric pressure), but there it stuck. These low pressures were beyond the range of the McLeod gauge and even beyond the Pirani gauge based on heat conduction from a hot filament (limit Torr), and it was necessary to... [Pg.405]

Thermal conductivity detector. The most important of the bulk physical property detectors is the thermal conductivity detector (TCD) which is a universal, non-destructive, concentration-sensitive detector. The TCD was one of the earliest routine detectors and thermal conductivity cells or katharometers are still widely used in gas chromatography. These detectors employ a heated metal filament or a thermistor (a semiconductor of fused metal oxides) to sense changes in the thermal conductivity of the carrier gas stream. Helium and hydrogen are the best carrier gases to use in conjunction with this type of detector since their thermal conductivities are much higher than any other gases on safety grounds helium is preferred because of its inertness. [Pg.241]

Thermal Conductivity Detector In the thermal conductivity detector (TCD), the temperature of a hot filament changes when the analyte dilutes the carrier gas. With a constant flow of helium carrier gas, the filament temperature will remain constant, but as compounds with different thermal conductivities elute, the different gas compositions cause heat to be conducted away from the filament at different rates, which in turn causes a change in the filament temperature and electrical resistance. The TCD is truly a universal detector and can detect water, air, hydrogen, carbon monoxide, nitrogen, sulfur dioxide, and many other compounds. For most organic molecules, the sensitivity of the TCD detector is low compared to that of the FID, but for the compounds for which the FID produces little or no signal, the TCD detector is a good alternative. [Pg.201]

In addition to developing solid RP structures, work has been conducted on sandwich structures such as filament-wound plastic skins with low-density foamed core or a plastic honeycomb core to develop more efficient strength-to-weight structures. Sandwich structures using a syntactic core have been successfully tested so that failures occurred at prescribed high-hydrostatic pressures of 28 MPa (4,000 psi). [Pg.112]

Therefore, before a final wall structure can be selected, it is necessary to conduct a combined strain analysis in both the longitudinal and hoop directions. This analysis will consider thermal contraction strains, the internal pressure, and the pipe s ability to bridge soft spots in the trench s bedding. In order to do this we must know more about the inherent properties of the material we are dealing with that is a structure made up of successive layers of continuous filament-wound fiberglass strands embedded within a plastic matrix. We must know the modulus of the material in the longitudinal direction and the... [Pg.213]

Fig. 3.3. Reaction vessel to investigate adsorption of H atoms on ZnO and conductivity. 1 - Filament 2 - Pt/PtRh = Thermocouple 3 Plate to measure conductivity of ZnO films 4 - ZnO film (adsorbent) 5 - Contacts 6,7 -Filament and thermocouple terminals... Fig. 3.3. Reaction vessel to investigate adsorption of H atoms on ZnO and conductivity. 1 - Filament 2 - Pt/PtRh = Thermocouple 3 Plate to measure conductivity of ZnO films 4 - ZnO film (adsorbent) 5 - Contacts 6,7 -Filament and thermocouple terminals...
Fig. 3.4. ZnO film conductivity as a function of amount of adsorbed hydrogen atoms. 1 - Film temperature -196 C filament temperature 1,000 C 2 — Film temperature -1% C filament temperature 1,100 C... Fig. 3.4. ZnO film conductivity as a function of amount of adsorbed hydrogen atoms. 1 - Film temperature -196 C filament temperature 1,000 C 2 — Film temperature -1% C filament temperature 1,100 C...
The experiment was carried out in a reaction cell shown in Fig. 3.3 with inner walls covered by a zinc oxide film having thickness 10 pm [20]. The surface area of the measuring film on the quartz plate was about 1/445 of the total film area on the wall of the vessel. The results of direct experimental measurements obtained when the adsorbent temperature was -196 C and temperature of pyrolysis filament (emitter of H-atoms) 1000°C and 1100°C, are shown on Fig. 3.4. One can see a satisfactory linear dependence between parameters A r (the change in film conductivity) and APh2 (reduction of hydrogen pressure due to adsorption of H-atoms), i.e. relations... [Pg.180]

Fig. 3.3. Relationship between the number of adsorbed H-atoms on the film and the number of electrons caused an increase in its conductivity. The calculation has been performed on the basis of experiments with the following film temperatures 1 - -33 C 2 - -78 C 3 -196 C. Filament temperature was fix at 1,100 C. Fig. 3.3. Relationship between the number of adsorbed H-atoms on the film and the number of electrons caused an increase in its conductivity. The calculation has been performed on the basis of experiments with the following film temperatures 1 - -33 C 2 - -78 C 3 -196 C. Filament temperature was fix at 1,100 C.
Fig. 3.7. Relationship between the stationary values of conductivity aha and the values of initial conductivity variation rates (.da/dOt-o = v for various temperatures of hot filament (i. e., various concentrations of H-atoms in the vessel volume). 1 - 300 C 2 - 380°C. Fig. 3.7. Relationship between the stationary values of conductivity aha and the values of initial conductivity variation rates (.da/dOt-o = v for various temperatures of hot filament (i. e., various concentrations of H-atoms in the vessel volume). 1 - 300 C 2 - 380°C.
Fig.4.4. Relative variation rate of the electric conductivity of the sensor D = (jda/dt)e as a function of the temperature of the pyrolysis filament, plotted in V - T axes (a) and Ig t - r axes (6). The temperatures in the vessel are 370 C (/) and 380 C (2), the pressure of hydrogen = 10 2 Torr. Fig.4.4. Relative variation rate of the electric conductivity of the sensor D = (jda/dt)e as a function of the temperature of the pyrolysis filament, plotted in V - T axes (a) and Ig t - r axes (6). The temperatures in the vessel are 370 C (/) and 380 C (2), the pressure of hydrogen = 10 2 Torr.

See other pages where Filament conductivity is mentioned: [Pg.305]    [Pg.667]    [Pg.305]    [Pg.667]    [Pg.340]    [Pg.336]    [Pg.15]    [Pg.165]    [Pg.218]    [Pg.218]    [Pg.290]    [Pg.291]    [Pg.295]    [Pg.295]    [Pg.1]    [Pg.333]    [Pg.764]    [Pg.1060]    [Pg.367]    [Pg.366]    [Pg.367]    [Pg.1018]    [Pg.237]    [Pg.241]    [Pg.765]    [Pg.89]    [Pg.358]    [Pg.237]    [Pg.95]    [Pg.309]    [Pg.319]    [Pg.182]    [Pg.182]    [Pg.184]   
See also in sourсe #XX -- [ Pg.305 ]




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