| 摘要 |
1,153,821. Combustion analysis. PERKIN-ELMER CORP. 4 Aug., 1966 [20 Aug., 1965], No. 35022/66. Heading B1X. [Also in Division G1] A method of quantitatively analysing an organic substance for carbon, hydrogen and nitrogen comprises burning a sample of the substance in the presence of oxygen in a combustion tube 14 to produce a gaseous mixture of combustion products which is trapped in a reservoir 52 at a known temperature and preselected superatmospheric pressure, a portion of the mixture from the reservoir being passed to atmosphere successively through cells 74, 80, 86 for measuring water, carbon dioxide and nitrogen respectively, each of the cells including a sample chamber 74a, 80a, 86a, and a reference chamber 74b, 80b, 86b, the component being measured by each all being effectively removed from the mixture as it passes between the sample and reference chambers thereof, and the thermal conductivity of the mixture being compared between the sample and reference chambers of each cell to indicate the amount of water, carbon dioxide and nitrogen respectively in the sample. In carrying out an analysis, the sample is burnt in a boat 18 introduced into the combustion tube 14 by way of an openable end 16 after the whole apparatus has been purged by a carrier gas such as helium from a tank 30. The sample is heated by coil 22 and oxygen is admitted from a tank 36. The sample burns and the gases pass through an oxidising agent 20 (copper oxide or cobaltous oxide) and then to a reduction tube 42 containing copper. The gaseous mixture then passes into the reservoir 52 which is provided with a pressure switch to close a valve 46 when a predetermined superatmospheric pressure has been reached. The reservoir 52 and cells 74, 80, 86 are contained in a constant temperature enclosure 12. The sample from the reservoir 52 is then allowed to pass under the action of the pressure in the reservoir, through a delay volume 64 and successively through the cells 74, 80, 86 to a vent 90. During this step some of the mixture escapes through a vent 70. Subsequently the gas in the delay volume 64 is caused to pass through the measuring cells using helium carrier gas from a line 94, so as to reach a steady state in the sample and reference chambers of the cells. The cell 74 has a trap 76 containing e.g. magnesium chlorate to absorb water vapour in the mixture as it passes from the sample chamber 74a to the reference chamber 74b. The thermal conductivities of the gases in the chamber 74a, 74b is compared using thermistors or hot filaments connected in a bridge circuit and coupled to a recorder 104. The cell 80 has a carbon dioxide trap 82 containing e.g. soda asbestos or lithium hydroxide. In the cell 86 the thermal conductivity of the gases remaining after removal of water and carbon dioxide is compared with that of the carrier gas from a line 92, and this gives the nitrogen content. The valves shown in the apparatus may be operated manually or automatically and in the correct sequence by use of cams. |
