Vacuum thermocouple

Figure 4.4.5. DifFerential vapor-pressure apparatus. 100 ml Pyrex flasks connected (a) to a differential pressure transducer (c) with digital readout (d) and (b) to vacuum pump (e) and absolute pressure vacuum thermocouple gauge (f). The constant temperature in the water bath is maintained by a temperature controller (g). The transducer and cormecting glassware are housed in an insulated box (i) and kept at constant temperature shghtly above the measuring temperature by controller (j). Polymer solution and pure solvent (here water) are stirred by underwater magnetic stirrers (h). [Reprinted with permission from Ref. 66, Copyright 1989, American Chemical Society].

Type J thermocouples (Table 11.58) are one of the most common types of industrial thermocouples because of the relatively high Seebeck coefficient and low cost. They are recommended for use in the temperature range from 0 to 760°C (but never above 760°C due to an abrupt magnetic transformation that can cause decalibration even when returned to lower temperatures). Use is permitted in vacuum and in oxidizing, reducing, or inert atmospheres, with the exception of sulfurous atmospheres above 500°C. For extended use above 500°C, heavy-gauge wires are recommended. They are not recommended for subzero temperatures. These thermocouples are subject to poor conformance characteristics because of impurities in the iron. 

The Type K thermocouple (Table 11.59) is more resistant to oxidation at elevated temperatures than the Type E, J, or T thermocouple, and consequently finds wide application at temperatures above 500°C. It is recommended for continuous use at temperatures within the range — 250 to 1260°C in inert or oxidizing atmospheres. It should not be used in sulfurous or reducing atmospheres, or in vacuum at high temperatures for extended times. 

The Type T thermocouple (Table 11.63) is popular for the temperature region below 0°C (but see under Type E). It can be used in vacuum, or in oxidizing, reducing, or inert atmospheres. 

Gauges. Because there is no way to measure and/or distinguish molecular vacuum environment except in terms of its use, readings related to gas-phase concentration ate provided by diaphragm, McCleod, thermocouple, Pitani gauges, and hot and cold cathode ionization gauges (manometers). 

Arc chutes, radiation generation equipment, vacuum tube components, thermocouples... 

A detonation flame arrester with an integral thermocouple at the inlet to the process heater firebox to prevent backflash into the vacuum system. 

An amine-terminated poly ether (ATPE) is prepared as follows. Charge poly(tetramethylene oxide) diol (PolyTHF 1000, BASF, 75.96 g, 0.0759 m) to a 500-mL three-neck round-bottom flask fitted with a thermocouple, a mechanical stirrer, and a vacuum port. Add tert-butylacetoacetate (24.04 g, 0.1582 m) and apply vacuum. Heat at 175° C for 4 h, Fourier transform infrared (FTIR) analysis should indicate complete loss of the polyol OH absorption at 3300 cm. The room temperature viscosity of the product should be about 520 mPa-s. React this acetoacetylated product (85.5 g, 0.0649 m) with cyclohexylamine (14.5 g, 0.1465 m) at 110° C under vacuum for several hours. Cool the resultant cyclohexylaminocrotonate poly ether product to room temperature (1790 mPa-s at room temperature). 

Figure 7.6. Experimental set up for temperature-programmed desorption in ultrahigh vacuum. The heat dissipated in the tantalum wires resistively heats the crystal the temperature is measured by a thermocouple spot-welded to the back of the crystal. A temperature programmer heats the crystal at a rate of typically 1-5 K s b Desorption of gases...

Figure 1. Schematic Diagram of the off-axis radiant heated reactor. A. cell body B. linear/rotary motion feedthrough C. transport rod D. projector bulb E. reflector F. insulated stainless steel enclosure G. air cooling port H. gas inlet I. gas outlet/pumping port J. chromel/alumel thermocouple K. high vacuum gate valve L, sample mount.

The catalyst for the in situ FTIR-transmission measurements was pressed into a self-supporting wafer (diameter 3 cm, weight 10 mg). The wafer was placed at the center of the quartz-made IR cell which was equipped with two NaCl windows. The NaCI window s were cooled with water flow, thus the catalyst could be heated to 1000 K in the cell. A thermocouple was set close to the sample wafer to detect the temperature of the catalyst. The cell was connected to a closed-gas-circulation system which was linked to a vacuum line. The gases used for adsorption and reaction experiments were O, (99.95%), 0, (isotope purity, 97.5%), H2 (99.999%), CH4 (99.99%) and CD4 (isotope purity, 99.9%). For the reaction, the gases were circulated by a circulation pump and the products w ere removed by using an appropriate cold trap (e.g. dry-ice ethanol trap). The IR measurements were carried out with a JASCO FT/IR-7000 sprectrometer. Most of the spectra were recorded w ith 4 cm resolution and 50 scans. 

Next to the inlet channels on the right and the left catalyst-loading channels are placed to insert suspensions with catalyst particles (by applying a vacuum at the exit). Thermocouple wells serve for temperature monitoring. 

Fig. 4.22. Reaction cell 1 - ZnO sensor 2 - evaporator of silver atoms 3 shutter used to terminate the beam of Ag atoms 4 - collimating apertures 5 an aperture used for pumping the cell out 6 - magnet 7 - magnetic drive for a shutter 8 - getter 9 — vacuum-measuring tube iO, 11 - electrodes 12 - thermocouple.

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