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YS/T 271.1-1994 PDF English

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YS/T 271.1-1994: Methods for chemical analysis of xanthates. The lead-acetate titration method for determination of xanthate content
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YS/T 271.1-1994: Methods for chemical analysis of xanthates. The lead-acetate titration method for determination of xanthate content


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GB NATIONAL STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA UDC 622.765.06.543.06 YS/T 271.1-1994 Renamed from GB 8150.1-87 Methods for chemical analysis of xanthates – The lead-acetate titration method for determination of xanthate content APPROVED ON. JANUARY 27, 1987 Implemented on. JUNE 01, 1988 Issued by. China Non-ferrous Metal Corporation

Table of Contents

1 Method summary... 3 2 Reagents... 3 3 Analytical procedures... 5 4 Calculation of analytical results... 6 5 Allowable difference... 6 Additional information... 7 Methods for chemical analysis of xanthates – The lead-acetate titration method for determination of xanthate content This standard complies with GB 1467-78 “Method for chemical analysis of metallurgy product - General rules and regulations”. This method is applicable to the determination of the amount of xanthogen in ethyl, isopropyl, n-butyl, isobutyl, n-pentyl, isopentyl and other sodium xanthate or potassium xanthate of lower carbon alkyl group.

1 Method summary

The sodium nitro-ferrocyanide is used as an indicator, the potassium ferricyanide is used to oxidize impurities such as alkali metal sulfides in xanthate into monomer sulfur to eliminate interferences. The chemical reaction is. Then the sodium rhodizonic acid is used as an indicator, and the lead acetate standard solution is used to titrate the sodium xanthate. The chemical reaction formula is.

2 Reagents

2.1 Hydrochloric acid (specific gravity 1.19). 2.2 Hydrochloric acid (6N). 2.3 Glacial acetic acid. 2.4 Aqueous ammonia solution (10%). 2.5 Ammonium-ammonium chloride buffer solution. Prepared in accordance with clause 38 (1) of GB 603-77 “Chemical reagent - Preparations of reagent solutions for use in test methods”. 2.6 Hexamethylenetetramine-hydrochloric acid buffer solution. DISSOLVE 300 g of hexamethylenetetramine in 500 ml of water, ADD 30 ml of hydrochloric acid (2.1), ADD water to dilute it to 1000 ml. 2.7 Potassium ferricyanide solution (1%). STORE it in a brown bottle, PREPARE it before use. 2.8 Chrome black T indicator solution (0.5%). WEIGH 0.5 g of chrome black T and 2 g of hydroxylamine hydrochloride, DISSOLVE it in 100 ml of ethanol. PREPARE it before use. 2.9 Xylenol orange indicator solution (0.2%). 2.10 Sodium nitro-ferrocyanide indicator solution (2%). PREPARE it before use. 2.11 Sodium rhodizonic acid indicator solution (0.1%). PREPARE it before use. 2.16.3 The equivalent concentration N of lead acetate standard solution is calculated as follows.

3 Analytical procedures

3.1 Distilled or deionized water for analysis. USE sodium hydroxide solution to adjust it to pH 6~7. 3.2 The xanthate specimen storage conditions are moisture and heat resistant, and the bottle caps are tightly closed. MINIMIZE uncovering time when analyzing. 3.3 USE the weighing bottle with lid to weigh 10.000 g of specimen, USE water to transfer it into a 500 ml volumetric flask, DILUTE it to the mark, SHAKE it uniformly, accurately TAKE 5.00 ml into a 250ml beaker. ADD 2 drops of sodium nitro-ferrocyanide indicator solution (2.10).

4 Calculation of analytical results

CALCULATE the percentage of xanthogenate by the following formula. Xanthogenate content (%) = (N • V • M/1000) / (5W/500) x 100

5 Allowable difference

The allowable difference of the parallel determination in this method is not more than 0.5%. ......
Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.


      

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