Method of analysis for determining very low sulfur levels in volatilizable samples

Claim 1

An iodometric method of analysis for determining very low levels of sulfur in volatilizable samples which contain sulfur and hydrocarbons which are convertible at least in part to unsaturated hydrocarbons by pyrolysis, which method comprises: (a) contacting a sample of known quantity with a flowing stream of a carrier gas and oxygen at a temperature in the range of 800° C. to 1000° C. and sufficiently high to pyrolyze and volatilize the sample and to effect the oxidation of oxidizable sulfur containing components therein to sulfur dioxide and sulfur trioxide; (b) conveying the pyrolyzed and volatilized components of said sample in the flowing stream of carrier gas through a fixed bed of cupric oxide maintained at a temperature in the range of about 650° C. to 800° C., whereby, sulfur dioxide and sulfur trioxide are quantitatively captured by the cupric oxide as copper sulfate and unsaturated hydrocarbons are oxidized so as to be noninterfering in an iodometric analysis; (c) after all of the sulfur oxides are quantitatively captured, removing the stream of carrier gas together with the oxidized unsaturated hydrocarbons from contact with said fixed bed, and then raising the temperature of the cupric oxide above 840° C. to decompose said copper sulfate and liberate sulfur dioxide, the rate of temperature increase being sufficiently high to complete the decomposition and liberation within a perod of time substantially less than the time of pyrolysis and volatilization in step (a); and (d) determining by iodometric titration the amount of sulfur dioxide which is liberated to determine the sulfur content of said sample by passing the carrier gas containing the liberated sulfur dioxide through an iodometric titration cell.

Claim 3

A method of analysis for determining very low levels of sulfur in volatilizable samples which contain sulfur and hydrocarbons which are convertible at least in part to unsatureated hydrocarbons by pyrolysis, which method comprises: (a) contacting a sample of known quantity with a flowing stream of a carrier gas and oxygen at a temperature in the range of 800° C. to 1000° C. and sufficiently high to pyrolyze and volatilize the sample and to effect the oxidation of oxidizable sulfur containing components therein to sulfur dioxide and sulfur trioxide; (b) conveying the pyrolyzed and volatilized components of said sample in the flowing stream of carrier gas through a fixed bed of cupric oxide maintained at a temperature in the range of about 650° C. to 800° C., whereby, sulfur dioxide and sulfur trioxide are quantitatively captured by the cupric oxide as copper sulfate and unsaturated hydrocarbons are oxidized so as to be noninterfering in an iodometric analysis; (c) after all of the sulfur oxides are quantitatively captured, removing the stream of carrier gas together with the oxidized unsaturated hydrocarbons from contact with said fixed bed, and then raising the temperature of the cupric oxide above 840° C. to decompose said copper sulfate and liberate sulfur dioxide; and (d) determining by iodometric titration the amount of sulfur dioxide which is liberated to determine the sulfur content of said sample.

Claim 4

A method of analysis for determining very low levels of sulfur in volatilizable samples which contain sulfur and hydrocarbons which are convertible at least in part to unsatureated hydrocarbons by pyrolysis, which method comprises: (a) contacting a sample of known quantity with a flowing stream of a carrier gas and oxygen at a temperature in the range of 800° C. to 1000° C. and sufficiently high to pyrolyze and volatilize the sample and to effect the oxidation of oxidizable sulfur containing components therein to sulfur dioxide and sulfur trioxide; (b) conveying the pyrolyzed and volatilized components of said sample in the flowing stream of carrier gas through a fixed bed of cupric oxide maintained at a temperature in the range of about 650° C. to 800° C., whereby, sulfur dioxide and sulfur trioxide are quantitatively captured by the cupric oxide as copper sulfate and unsaturated hydrocarbons are oxidized so as to be noninterfering in an iodometric analysis; (c) after all of the sulfur oxides are quantitatively captured, removing the stream of carrier gas together with the oxidized unsaturated hydrocarbons from contact with said fixed bed, and then raising the temperature of the cupric oxide above 840° C. to decompose said copper sulfate and liberate sulfur dioxide; and (d) determining by iodometric titration the amount of sulfur dioxide which is liberated to determine the sulfur content of said sample.