Method and Apparatus for Gas Filter Testing
A method is described to determine the remaining sorption capacity of activated-carbon-sorbent gas filters by measuring the breakthrough time for a test gas challenge to a test filter with known and controlled test conditions that include flow rate and temperature and the use of a calibration curve that has been established by prior testing of the test filter sorbent medium in calibration tests where the filter is exposed to a known quantity of gas surrogate for the challenge gases that the filter may sorb in service and then testing the test filter medium by challenge with a sparged gas that can be selectively detected to determine the breakthrough as a function of test gas. The apparatus using such a method comprises a portable system that includes a sparging test gas generator, a carrier gas system, a test filter canister holder, and a selective detector that can quantitatively monitor the test gas exiting the test filter canister. The method and apparatus can be used to determine the remaining sorption capacity of activated carbons filters, e.g., ASZM-TEDA carbon filters such as those used for building defense against chemical toxant attack, industrial accidents, and for tactical collective protection and for industrial ventilation and compliance with environmental regulations.
1 . A method to determine the remaining sorption capacity of an activated carbon filter comprising:
selecting a test gas;
performing a calibration procedure to generator a calibration graph (curve);
inserting a test filter into the gas flow circuit of the test apparatus with temperature control of the sparging gas generator, gas flow circuit, and test filter;
determining the breakthrough time; and
using the calibration curve to determine the remaining sorption capacity of the test filter.
2 . The method of claim 1 wherein the test gas is selected to have a sufficiently low boiling point so that condensation of the test gas is avoided at the test operation temperature.
3 . The method of claim 2 wherein the test gas is a halogenated compound.
4 . The method of claim 2 wherein the test gas is halogenated but not fluorinated and the determination of breakthrough time is performed using a dry electrolytic conductivity detector.
5 . The method of claim 2 wherein the test gas is selected to be dichloromethane.
6 . The method of claim 2 wherein the mock contaminant compound is either one or a mixture of both of the group consisting of dimethyl methylphosphonate and 2-chloroethyl methyl ether.
7 . The method of claim 2 wherein the calibration curve is generated by performing the step of adding a Mock Contaminant gas to the activated carbon by using a low toxicity organic compound to saturate a portion of the activated carbon and then performing the additional steps of:
mixing the said Mock Contaminant saturated carbon with the fresh activated carbon;
packing the mixture into an empty canister with a selected ratio of fresh and saturated carbon;
measuring the breakthrough time, so that the breakthrough time vs fraction of fresh carbon is determined; and subsequently
repeating the said mixing, packing, and measuring for a set of various ratios of fresh and saturated carbon; and optionally
repeating the above steps with additional selected test operation conditions selected from the group consisting of temperature, carrier gas flow rate, sparging gas flow rate, and breakthrough time range, to generate a set of calibration curves.
8 . The method of claim 1 , further comprising the step of:
correlating the results for the test canister to a main filter.
9 . An apparatus for the determination of the remaining sorption capacity of an activated carbon filter by the method of claim 1 , said apparatus comprising:
a carrier gas supply and a gas sparging gas generator that provides a selected test gas, said supply and generator having gas regulation and thermal and flow stabilization;
a test canister connection system that is a canister holder that permits easy emplacement of a test canister or connection means so that an isolated test canister can be inserted into the test gas/carrier gas flow system of the test apparatus;
a temperature control means for the test canister, gas supply, and test gas generator circuit;
a selective detector of the test gas; and
a data acquisition and instrument control system, which includes operating software and a computer with a display.
10 . The apparatus of claim 9 wherein the selective detector is an electron capture device.
11 . The apparatus of claim 9 wherein the selective detector is a dry electrolytic conductivity detector.
12 . The apparatus of claim 9 wherein the test gas is dichloromethane.
13 . The apparatus of claim 9 wherein the mock contaminant compound is either one or a mixture of both of the group consisting of dimethyl methylphosphonate and 2-chloroethyl methyl ether.
14 . The apparatus of claim 9 , further comprising:
a stable gas-split system.