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Oxidation tubing

Fig. 12.75Section through zirconium oxide cell 1, zirconium oxide tube 2, NTC resistor 3, dosing electrodes 4, ceramic spacer 5, measuring electrodes 6, thermal insulation 7, heating coil 8, thermocouple Source Own files... [Pg.371]

Kobayashi S, Hamasaki N, Suzuki M, Kimura N, Shirai H, Hanabusa K (2002) Preparation of helical transition-metal Oxide tubes using organogelators as structure-directing agents. J Am Chem Soc 124 6550-6551... [Pg.358]

The liberated acid is titrated to obtain a measure of the phosphide phosphorus. The gas emerging from the solution is swept into a hot copper oxide tube to convert the hydrogen to water the latter is collected in a weighed drying tube. [Pg.25]

The combustion chamber was a round channel 9.53 mm in diameter and 0.864 m long. The first 0.623 m was confined by a high purity, aluminum oxide tube. The final 0.241 m consisted of the central hole of an aluminum oxide block formed from WulflE furnace elements. The tube was insulated with 6.4 mm of powdered alumina surrounded by a larger aluminum oxide tube which was in turn insulated with glass fibers. Propane-air flames in six equidistant surroimding channels acted as guard heaters in the block. The block was insulated with powdered alumina. [Pg.85]

Weight of copper oxide tube before the experiment Weight of copper oxide tube after the experiment. Weight of drying tube after the experiment. . . Weight of drying tube before the experiment. . ... [Pg.103]

Loss of copper oxide tube in grams, respectively, 8.051, 10.832, and 8.246. [Pg.103]

The rotational speed and angle at which it is positioned control the residence time of the solid in the kiln. Normally solid waste is converted into CO, particulate matter, or ash. For complete oxidation of flue gases and particulate matter, the kiln is also provided with a secondary combustion chamber. The volatilized combustibles exit the kiln and enter the secondary chamber where a complete oxidation tube is placed. [Pg.79]

The most simple form is a single, uniformly structured wall of a certain material, the so-called symmetric, stand-alone membranes. Examples are dense metal or oxide tubes and porous hollow fibres. To obtain sufficient mechanical strength, single-walled symmetric systems usually have a considerable thickness. [Pg.22]

Fig. 7.3 Diagram of analyser for continuous monitoring of total mercury in water 1 and 1 , peristaltic pumps 2, 2 , 2" and 3, merging points 4, reaction-oxidation tube 4 , reduction-extraction tube 5, gas-liquid separator 6, condenser 7, UV flow-cell 8, UV spectrophotometer 9, recorder 10, mercury vapour absorber 11, water-bath (O C) A-E, sample, reductant, reagent, acid and oxidant stream, respectively. (Reproduced from [1] with permission of the Royal Society of Chemistry). Fig. 7.3 Diagram of analyser for continuous monitoring of total mercury in water 1 and 1 , peristaltic pumps 2, 2 , 2" and 3, merging points 4, reaction-oxidation tube 4 , reduction-extraction tube 5, gas-liquid separator 6, condenser 7, UV flow-cell 8, UV spectrophotometer 9, recorder 10, mercury vapour absorber 11, water-bath (O C) A-E, sample, reductant, reagent, acid and oxidant stream, respectively. (Reproduced from [1] with permission of the Royal Society of Chemistry).
Amine 220 was used as a coating substrate for the detection of vinyl chloride in the linear range of 0.6 - 75 PPm (63). Vinyl chloride was passed through chromate oxidation tubes (DrSger), where the reaction products were detected with the coated crystal. It was suspected that the amine 220 responds to the HCl reaction product but other decomposition materials caused an irreversibility problem. The chromate oxidation tube had a lifetime of 75 injections of 2.5 cc of 33 ppm vinyl chloride, however, after 17-20 Injections the response decreased drastically and the coating was overloaded with coating-reaction products complex adsorbed on the crystal. [Pg.294]

A critical point in the work presented in this communication was the generation of a steady stream of silicon atoms which have to be condensed together with the substrate molecule and an excess of matrix material onto the cooled window. In our early experiments, silicon was vaporized from a tantalum Knudsen cell (Figure 1.2, Type A) or a boron nitride crucible which was surrounded by an aluminum oxide tube. The oven was resistively heated to temperatures of 1490-1550 °C by means of a tungsten wire wound around the alumina tube (Figure 1.2, Type B). In later runs, a rod of dimensions 0.7-2-22... [Pg.8]

Knudsen cell Boron nitride crucible Rod (0.7x2 x22mm) tantalum aluminum oxide tube of doped silicon virafer ... [Pg.9]

Figure 5.16 Synthesis of PCL-grafted CNTs by the ROP approach and degradation of PCL chains by PS lipase (top), and representative SEM images of the control experiment sample which was collected from the phosphate buffer solution of MWCNT-g-PCL (52.7 wt% of PCL) without PS lipase after 96 h (a), and the samples of MWCNT-g-PCL degraded with PS lipase for 24 h (b), 48 h (c) and 96 h (d). The scale bars in (a), (b), (c) and (d) represent 1000, 500, 500 and 500 nm, respectively. The marked tubes 1 and 2 have diameters of ca. 90.3 and 85.5 nm, respectively. After 24 h of degradation with PS lipase (b), the diameters of tubes 3 and 4 are ca. 83.3 and 75.7 nm, respectively. After 48 h of degradation (c), the diameters of tubes 5 and 6 are only ca. 54.1 and 50.5 nm, respectively. After 96 h of degradation (d), little residual polymer on the surfaces of MWCNTs can be detected, and many tubes with diameters of ca. 20-30 nm are found (tubes 7 and 8 have diameters of 22.7 and 28.2 nm, respectively). In this case, the average diameter of the degraded tubes is almost equal to that of the oxidized tubes. Reprinted with permission from Zeng et al. ... Figure 5.16 Synthesis of PCL-grafted CNTs by the ROP approach and degradation of PCL chains by PS lipase (top), and representative SEM images of the control experiment sample which was collected from the phosphate buffer solution of MWCNT-g-PCL (52.7 wt% of PCL) without PS lipase after 96 h (a), and the samples of MWCNT-g-PCL degraded with PS lipase for 24 h (b), 48 h (c) and 96 h (d). The scale bars in (a), (b), (c) and (d) represent 1000, 500, 500 and 500 nm, respectively. The marked tubes 1 and 2 have diameters of ca. 90.3 and 85.5 nm, respectively. After 24 h of degradation with PS lipase (b), the diameters of tubes 3 and 4 are ca. 83.3 and 75.7 nm, respectively. After 48 h of degradation (c), the diameters of tubes 5 and 6 are only ca. 54.1 and 50.5 nm, respectively. After 96 h of degradation (d), little residual polymer on the surfaces of MWCNTs can be detected, and many tubes with diameters of ca. 20-30 nm are found (tubes 7 and 8 have diameters of 22.7 and 28.2 nm, respectively). In this case, the average diameter of the degraded tubes is almost equal to that of the oxidized tubes. Reprinted with permission from Zeng et al. ...
The same stock of alloys as used for making the coupons of rack 1 was used for the coupons of racks 2 and 3. However, the aluminium oxide tubes and rings that were used in rack 1 were no longer available from the same vendor. Consequently these parts were made from a different lot of materials, and this resulted in some delay and additional costs. The aluminium and stainless steel coupons were marked using a laser scriber. These marks indicated the material and identified the coupon. The following changes were also introduced during the manufacture of coupons for racks 2 and 3. [Pg.147]

Currently, this relatively robust and optimized type of cell testing housing is used for all single-ceU measurements (Figure 9.18b). In the bottom plate of the measuring housing, aluminum oxide tubes have been cemented in place to provide connections to the gas dehvery system. [Pg.270]

The reduced pressure side of the aspirator was connected to the side limb of the oxidation tube by means of a silicon rubber sleeve. It is seen from Figure 17 that the two-tube system in the normal wire director has been replaced by a single tube. The oxygen or air is fed in at the center of this tube, providing both the evaporator flow and the oxidation flow. The oxidation and cleaning tubes were constructed from quartz. [Pg.113]

There are two basic designs of SOFC units. In the planar design, components are assembled in flat stacks where the air and hydrogen traditionally flow though the unit via channels built into the anode and cathode. In the tubular design, air is supplied to the inside of an extended solid oxide tube (which is sealed at one end), whilst fuel flows round the outside of the tube. The tube itself forms the cathode, and the cell components are constructed in layers around the tube. [Pg.38]

A US company has been developing a fuel cell based on a ceramic oxide electrolyte to operate at about 1000° C. It is able to consume either hydrogen or hydrogen-carbon monoxide mixtures (reformed natural gas, etc.) as the anode fuel. Unlike all the other systems which are based on stacks of parallel porous electrodes, the design here is centred on a ceramic oxide tube and cylindrical electrodes. A number of 3 kW units with 144 cells are under test to check performance and to ascertain lifetime under practical conditions. A high electrical efficiency of > 50% has been achieved in early tests and very useful waste heat is available from this high-temperature cell. [Pg.594]

Kang N, Park JH, Choi J, Jin J, Chun J, Jung IG, Jeong J, Park JG, Lee SM, Kim HJ, Son SU (2012) Nanoparticulate iron oxide tubes from microporous organic nanotubes as stable anode materials for lithium ion batteries. Angew Chem Int Ed 51 6626-6630... [Pg.426]


See other pages where Oxidation tubing is mentioned: [Pg.302]    [Pg.355]    [Pg.11]    [Pg.40]    [Pg.64]    [Pg.291]    [Pg.328]    [Pg.310]    [Pg.695]    [Pg.288]    [Pg.514]    [Pg.83]    [Pg.109]    [Pg.93]    [Pg.187]    [Pg.332]    [Pg.210]    [Pg.363]    [Pg.363]   
See also in sourсe #XX -- [ Pg.97 ]




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