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GB/T 14571.5-2016 PDF English


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GB/T 14571.5-2016: PDF in English (GBT 14571.5-2016)

GB/T 14571.5-2016 NATIONAL STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA ICS 71.080.60 G 16 Test method of monoethylene glycol for industrial use - Part 5: Determination of chloride ion – Ion chromatography ISSUED ON: OCTOBER 13, 2016 IMPLEMENTED ON: MAY 01, 2017 Issued by: General Administration of Quality Supervision, Inspection and Quarantine; Standardization Administration of the People's Republic of China. Table of Contents Foreword ... 3  1 Scope ... 4  2 Normative references ... 4  3 Method summary ... 4  4 Reagents and materials ... 5  5 Instruments and devices ... 6  6 Sampling ... 9  7 Analysis steps ... 9  8 Calculation of analysis results ... 10  9 Expression of analysis results ... 10  10 Precision ... 10  11 Quality control ... 11  12 Report ... 11  Test method of monoethylene glycol for industrial use - Part 5: Determination of chloride ion - Ion chromatography WARNING: This Part is not intended to describe all security issues related to its use. It is the responsibility of the user to take appropriate safety and health measures to ensure the compliance with relevant national regulations. 1 Scope This Part of GB/T 14571 specifies ion chromatography for determination of chloride ion in ethylene glycol for industrial use. This Part is applicable to determine the chloride ion of which the concentration range is 0.01mg/kg~1.0mg/kg in ethylene glycol for industrial use. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. GB/T 3723, Sampling of chemical products for industrial use - Safety in sampling GB/T 6680, General rules for sampling liquid chemical products GB/T 6682, Water for analytical laboratory use - Specification and test methods GB/T 8170, Rules of rounding off for numerical values & expression and judgement of limiting values 3 Method summary Use syringe extraction method to introduce sample into sample loop. Load into the anion exchange column from the eluent via a six-way valve. Separate chloride ion and other anions. Use conductivity detector to detect. Chloride ion a) Sodium carbonate / sodium bicarbonate stock solution (4.5mol/L sodium carbonate and 0.8mol/L sodium bicarbonate solution): before use, at 270°C~300°C, burn sodium carbonate (4.4) to constant weight. Weigh 47.70g of sodium carbonate and 6.72g of sodium bicarbonate (4.5). Place into a 100mL volumetric flask. Use water to dissolve. Set volume. Prepare and obtain 4.5mol/L sodium carbonate and 0.8mol/L sodium bicarbonate mixed solution as sodium carbonate / sodium bicarbonate stock solution. Seal and store in a refrigerator freezer. The validity does not exceed 3 months; b) Sodium carbonate / sodium bicarbonate eluent (4.5mmol/L sodium carbonate and 0.8mmol/L sodium bicarbonate solution): use water to dilute the above sodium carbonate / sodium bicarbonate stock solution. Mix well. Prepare 4.5mmol/L sodium carbonate and 0.8mmol/L sodium bicarbonate solution, as eluent. Prepare when required. 4.11 Potassium hydroxide eluent: 5mmol/L potassium hydroxide solution. It is recommended to use eluent generator to generate. It may also prepare according to the following methods: a) Potassium hydroxide stock solution (5mol/L): weigh 28.05g of potassium hydroxide (4.3) in a 100mL volumetric flask. Use water to dissolve. Set volume. Prepare and obtain 5mol/L potassium hydroxide solution as eluent stock solution. Seal and store in a refrigerator freezer. The validity does not exceed 3 months; b) Potassium hydroxide eluent (5mmol/L): use water to dilute the above potassium hydroxide stock solution. Mix well. Prepare 5mmol/L potassium hydroxide solution as eluent. Prepare when required. 5 Instruments and devices 5.1 Ion chromatograph 5.1.1 Eluent pump: the parts of the pump that contact the eluent shall be non- metallic and resistant to strong acids and bases. It may use nitrogen to replace pump delivery eluent. 5.1.2 Eluent generator (optional): automatically generate the desired concentration of eluent. 5.1.3 Anion trap column (optional): when using an eluent generator (5.1.2), use anion trap column to remove anions from the eluent generator. 5.1.4 Sample injection device: including six-way valve, sample loop and syringe. the chromatogram to determine the retention time of chloride ions. Take the chloride ion concentration as the abscissa and the peak area as the ordinate to draw the standard curve or calculate the linear regression equation. The linear correlation coefficient shall be no less than 0.99. 7.3 Sample determination Under the same test conditions as the analytical standard solution, analyze and determine the sample. NOTE 1: If the chloride ion content in the sample exceeds the highest concentration range of the standard curve, it may use ethylene glycol (4.6) to dilute the sample and analyze it. NOTE 2: The determination results may be interfered with by chloride ions in volumetric flasks, glassware, eluents and reagents. Ensure that test volumetric flasks, glassware, and instruments are not contaminated with chloride ions. When contacting with samples and reagents, it needs to wear rubber gloves to avoid chloride ion contamination. NOTE 3: Under the recommended test conditions, if the method is running out of time, anions eluted after chloride ions may enter the next sample analysis process and interfere chloride ion determination. 8 Calculation of analysis results According to the peak area of chloride ion, its concentration is determined by the corresponding standard curve (mg/kg). 9 Expression of analysis results For any sample, use the arithmetic mean of the results of two repeated measurements to report the analysis results. Round off to 0.01mg/kg according to GB/T 8170. 10 Precision 10.1 Repeatability In the same laboratory, the same operator uses the same device. According to the same test method, test the same test object independently of each other in a short time. The absolute difference between the two independent test results obtained is not greater than the repeatability limit (r) listed in Table 3. The premise is that the case greater than the repeatability limit (r) does not exceed 5%. ......
 
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.