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Publication numberUS3598531 A
Publication typeGrant
Publication dateAug 10, 1971
Filing dateSep 19, 1968
Priority dateSep 19, 1968
Publication numberUS 3598531 A, US 3598531A, US-A-3598531, US3598531 A, US3598531A
InventorsBremanis Elmars
Original AssigneeUniversal Oil Prod Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method for determining sulfur as sulfur dioxide
US 3598531 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 015cc U.S. Cl. 23-230 2 Claims ABSTRACT OF THE DISCLOSURE Chloride compound and nitrogen interferences to the iodometric and/or microcoulometric methods of sulfur determination are overcome by adding sodium azide to the titration cell electrolyte. The improved method is applicable to oils, crudes, solids, and petrochemicals.

BACKGROUND OF THE INVENTION The presence of chlorine in concentrations in excess of 1.0% and nitrogen in excess of 0.1% may interfere in the iodometric determination of sulfur in petroleum and chemical products using the classical iodometric ASTM Method of Test for Sulfur in Petroleum Products (High Temperature Method) (D 1552-64) or its equivalent. In the case of nitrogen, the extent of such interference is dependent on the type of nitrogen compound as well as the amount present. The interference results from oxidation of nitrogen to oxides of nitrogen and chloride to chlorine, each of which reacts with potassium iodide in the iodometric titration to liberate iodine. Sulfur is oxidized in the method to sulfur dioxide which is measured by the consumption of iodine in the titration. Therefore, the effect of the presence of nitrogen and chlorine is to cause low, or even negative results. Since chloride and especially nitrogen are commonly associated with sulfur in petroleum products, petrochemicals, and chemicals, this interference constitutes a very severe limitation of the method.

Therefore, it is one object of this invention to provide an improved method for determining sulfur as sulfur dioxide in petroleum and chemical products. It is another object of this invention to provide a method of overcoming nitrogen and chloride compound interferences in the classical methods of sulfur determination so that the inherent limitations of the old methods are eliminated.

In one embodiment, our invention provides an improvement in the method for determining sulfur as sulfur dioxide in petroleum, petrochemical, and chemical products utilizing the iodometric or microcoulometric methods of sulfur determination wherein a titration cell containing an iodine-containing titration solvent is utilized, said improvement comprising overcoming chloride compound and nitrogen interferences in said method by adding sodium azide to the titration solvent thereby preferentially reacting the chloride compounds and nitrogen compounds without reacting the iodine.

SUMMARY OF THE INVENTION AND EXAMPLE In order to overcome the interference from nitrogen, several scrubbers and pretreatments were evaluated. From this experimentation, it was found that an alkali metal 3,598,531 Patented Aug. 10, 1971 azide, and preferably sodium azide, added directly to a titration vessel, appeared to react rapidly and preferentially with chlorine and the oxides of nitrogen. The presence of sodium azide did not appear to otherwise participate in or interfere with the iodometric determination of sulfur as sulfur dioxide. To check these preliminary observations, several standards were analyzed with and without the presence of sodium azide in the titration vessel of the volumetric-type sulfur determinator, and in the coulometric-type sulfur analyzer as described in Adams et al., Improved Sulfur-Reacting Microcoulometric Cell for Gas Chromatography, Analytical Chemistry, vol. 38, 1966, p. 1094.

An induction furnace and automatic volumetric sulfur apparatus was used where the test method called for a volumetric-type sulfur determinator. A microcoulometer with a 300 P cell Was used for iodine generation where the method called for a coulometric-type sulfur analyzer. The combustion train used with the microcoulometer employed a 13 mm. outside diameter, 10 mm. inside diameter, ll5-cm. quartz tube filled with quartz chips, coarsely ground to pass a inch screen. The quartz tube was maintained at 1150 C. using two heavy duty combustion furnaces in series. Oxygen carrier fiow rates from 20 to 300 mL/min. were preferred, although a flow of 50 ml./ min. was normally used with this apparatus. Sodium azide (practical) was used as the reagent.

For the coulometric analyses, 3 to 5 mg. of solid sodium azide was added to the titration cell solvent. In order to equilibrate the system prior to the first determination, a sample of S0 gas was injected or a sample of the product was burned. A fresh portion of sodium azide was added whenever the cell solvent was changed.

For the volumetric-type determinations, 500 to 700 mg. of solid sodium azide was added to the titration cell solvent prior to each determination. No other changes in the normal operating procedures for the method are required for either approach to the iodometric sulfur analysis. To determine the efficacy of sodium azide addition in overcoming nitrogen and chlorine interference, several standards and samples were analyzed with and without added sodium azide. The data in Table 1 comparing both the coulometric and volumetric methods were obtained:

Therefore, it can be concluded that sodium azide added to an iodine-containing titration solvent is effective in overcoming the interference from chloride compounds and nitrogen where it is encountered in the iodometric determination of sulfur as sulfur dioxide. For ASTM Method D 1552 modified by the improvement of my invention, the relative error in the presence of about 20% chlorine and about 8% nitrogen was 2.2%; the relative standard deviation was 2% for the 1 to 20% sulfur level. For the coulometric sulfur method, the relative error in the presence of about 8% nitrogen was about -1.0% and the relative standard deviation was 1.1%. As shown below, samples analyzed included oils, crudes, and solids and included sulfur levels ranging from about 0.1 to about 20%. The coulometric method is more sensitive and has better precision than the volumetric method although the two methods are comparable in accuracy, even in the presence of large amounts of nitrogen and chlorine compounds provided the improvement of my invention, namely, the addition of sodium azide to the titration solvent is utilized.

TABLE 1.ANALYSIS OF STANDARDS AND SAMPLES WITH AND WITHOUT ADDED SODIUM AZIDE Percent sulfur found NaNa added Volumetric Percent present No NaNs added 01 S Volumetric Coulometric Coulometrie 1 Black Negative Sample 0 3028278382 do-10100431 m 22 2 L5 5 A-0 1 1 7 3 1 1011 2 2 2 L Black do 78 n u n m m m n u n n w u U n d e "m M m m am mmm mm ue. 1 Ma m0 0 3 n. H d S v. u nn wn B mn H 86H a tz h S S 1 Ye M C CBC Atv l Generates iodine; gives black solution in the volumetric method and a negative response in the case of the coulometric method it much nitrogen is present.

2 Oxygen bomb analysis, ASTM Method of Test for Sulfur in Petroleum Products by the Bomb Method (D 129-64).

References Cited UNITED STATES PATENTS I claim:

1. In a method for determining sulfur as sulfur dioxide in petroleum, petrochemical, or chemical products 25 which contain sulfur, nitrogen and chlorine utilizing the 2669504 2/1954 Halvorson 6t 23230PC iodometric or microcoulometric methods of sulfur deter- OTHER REFERENCES Pardue et al., Chem. Abstr. 58, 7125d (1963).

mination wherein a titration cell containing an iodine-containing titration solvent is utilized to measure sulfur di- MORRIS O. WOLK, Primary Examiner R. M. REESE, Assistant Examiner which comprises adding an alkali metal azide to said titration solvent thereby preferentially reacting said chlorine and nitrogen without reaction of said iodine.

US. Cl. X.R.

2. The method of claim 1 wherein said alkali metal 35 azide is sodium azide. 204-1

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3853474 *Oct 10, 1972Dec 10, 1974IttMethod of burning combustible fluids for further analysis
US4172705 *Apr 12, 1978Oct 30, 1979Envirotech CorporationProcess and apparatus for sulfur analysis
US4211748 *Jan 23, 1978Jul 8, 1980International Telephone And Telegraph CorporationStack gas analyzer and thermal oxidation device therefor
US4325911 *May 20, 1980Apr 20, 1982International Telephone And Telegraph CorporationStack gas analyzer and thermal oxidation device therefor
Classifications
U.S. Classification436/123, 205/785.5, 205/786.5, 436/51, 205/782
International ClassificationG01N33/28, G01N33/26, G01N31/16
Cooperative ClassificationG01N33/287, G01N31/16
European ClassificationG01N33/28G6, G01N31/16