Analytical method for the determination of less than five ppm of sulfur in nickel

An analytical technique for the separation and determination of less than 5 ppm of S has been developed. Ten grams of Ni are dissolved at room temperature in a solution of 0.9M in both cupric potassium chloride and hydrochloric acid. The resulting residue contains all of the S. The residue is separa...

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Veröffentlicht in:Analytical chemistry (Washington) 1974-06, Vol.46 (7), p.882-885
1. Verfasser: Burke, Keith E
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description An analytical technique for the separation and determination of less than 5 ppm of S has been developed. Ten grams of Ni are dissolved at room temperature in a solution of 0.9M in both cupric potassium chloride and hydrochloric acid. The resulting residue contains all of the S. The residue is separated on a S-free filter, washed, dried and burned in a stream of 0 to convert all of the S to sulfur dioxide. The resulting sulfur dioxide is titrated with a standard solution of potassium iodate. The proposed analytical technique gives accurate results for the determination of S in the range from 0.2-20 ppm. The precision is +0.7 ppm for the 2 ppm level. The method is also applicable to Al, Fe, Co and Cu, as well as their alloys. 13 ref.--AA.
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Ten grams of Ni are dissolved at room temperature in a solution of 0.9M in both cupric potassium chloride and hydrochloric acid. The resulting residue contains all of the S. The residue is separated on a S-free filter, washed, dried and burned in a stream of 0 to convert all of the S to sulfur dioxide. The resulting sulfur dioxide is titrated with a standard solution of potassium iodate. The proposed analytical technique gives accurate results for the determination of S in the range from 0.2-20 ppm. The precision is +0.7 ppm for the 2 ppm level. 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Chem</addtitle><description>An analytical technique for the separation and determination of less than 5 ppm of S has been developed. Ten grams of Ni are dissolved at room temperature in a solution of 0.9M in both cupric potassium chloride and hydrochloric acid. The resulting residue contains all of the S. The residue is separated on a S-free filter, washed, dried and burned in a stream of 0 to convert all of the S to sulfur dioxide. The resulting sulfur dioxide is titrated with a standard solution of potassium iodate. The proposed analytical technique gives accurate results for the determination of S in the range from 0.2-20 ppm. The precision is +0.7 ppm for the 2 ppm level. 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Chem</addtitle><date>1974-06-01</date><risdate>1974</risdate><volume>46</volume><issue>7</issue><spage>882</spage><epage>885</epage><pages>882-885</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><abstract>An analytical technique for the separation and determination of less than 5 ppm of S has been developed. Ten grams of Ni are dissolved at room temperature in a solution of 0.9M in both cupric potassium chloride and hydrochloric acid. The resulting residue contains all of the S. The residue is separated on a S-free filter, washed, dried and burned in a stream of 0 to convert all of the S to sulfur dioxide. The resulting sulfur dioxide is titrated with a standard solution of potassium iodate. The proposed analytical technique gives accurate results for the determination of S in the range from 0.2-20 ppm. The precision is +0.7 ppm for the 2 ppm level. The method is also applicable to Al, Fe, Co and Cu, as well as their alloys. 13 ref.--AA.</abstract><pub>American Chemical Society</pub><doi>10.1021/ac60343a013</doi><tpages>4</tpages></addata></record>
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title Analytical method for the determination of less than five ppm of sulfur in nickel
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