This standard specifies the technical requirements, test methods, inspection rules, packaging and marking of chemical reagent petroleum ether. This standard applies to the inspection of chemical reagent petroleum ether. GB/T 15894-1995 Chemical reagent petroleum ether GB/T15894-1995 Standard download decompression password: www.bzxz.net
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National Standard of the People's Republic of China Chemical reagent Petroleum ether GB/T 15894—1995 This standard is equivalent to R73\Petroleum solvent oil 40/60" in the international standard ISO6353-3—1987 "Chemical analysis reagents—Part 3: Specifications—Second batch". This reagent is a colorless, transparent, volatile liquid with a special odor. It is extremely flammable and insoluble in water. It is miscible with ethanol, benzene, chloroform, carbon disulfide, ether and oils. 1 Subject content and scope of application This standard specifies the technical requirements, test methods, inspection rules, packaging and marking of the chemical reagent petroleum aldehyde. This standard applies to the inspection of the chemical reagent petroleum ether. 2 Reference standards GB/T601 GB/T602 GB/T 603 GB/T605 GB/T606 GB/T 615 GB/T619 GB/T 6682 GB/T 9723 GB/T9728 GB/T 9736 GB/T 9737 GB/T9740 HG 3—119 3 technical requirements 3.1 Boiling range (℃): Chemical reagents Chemical reagents Chemical reagents Chemical reagents Chemical reagents Chemical reagents Chemical reagents Chemical reagents Preparation of standard solutions for titrimetric analysis (volumetric analysis)Preparation of standard solutions for determination of impurities Preparation of preparations and products used in test methodsGeneral method for colorimetric determination General method for determination of water content (Karl Fischer method)General method for determination of boiling range Sampling and testing Collection rules Specifications and test methods for water used in analytical laboratoriesChemical reagents Chemical reagents Chemical reagents Chemical reagents Chemical reagents Chemical reagents General rules for flame atomic absorption spectrometry General method for determination of sulfate General method for determination of acidity and alkalinity General rules for determination of easily carbonizable substances General method for determination of evaporation residue Packaging and marking Class I||tt ||Class 1 Class I·Www.bzxZ.net 3.2 Chroma: ≤10 black unit Approved by the State Administration of Technical Supervision on December 20, 1995 30~60 ?60~90, ?90~120. Implemented on August 1, 1996 3.3 Maximum impurity content: Evaporation residue Water content (H, O) Acidity (in terms of H+), mmol/100g 4 Test Method GB/T15894—1995 Analytically pure Sulfur compounds (measured as SO,) Iron (Fe) Lead (Pb) Easily carbonizable substances Analytically pure The standard titration solution, impurity standard solution, preparation and products in this test method shall be prepared in accordance with the provisions of GB/T601, GB/T602 and GB/T603 unless otherwise specified. The experimental water shall meet the specifications of Grade 3 water in GB/T6682. 4.1 Boiling range determination Determine in accordance with the provisions of Chapter 5 of GB/T615. The volume of the retained material within the specified temperature shall not be less than 90.0mL. 4.2 Chroma determination Measure 50mL of the sample, inject it into a 100mL colorimetric tube, and determine it in accordance with the provisions of GB/T605. 4.3 Determination of impurities The sample should be measured accurately to 0.1 mL. 4.3.1 Evaporation residue Measure 155 mL (100 g) of the sample, place it in the evaporation blood that has been constant weight at 105±2℃, evaporate it to dryness on a water bath, and dry it in an electric oven at 105±2℃ to constant weight. The result is calculated according to the provisions of Chapter 5 of GB/T9740. 4.3.2 Moisture Measure 15.5 mL (10 g) of the sample, use 10 mL of methanol and 10 mL of chloroform as solvent, and determine it according to the provisions of GB/T606. 4.3.3 Acidity Measure 100 mL of carbon dioxide-free water, add 2 drops of methyl red indicator (1 g/L), and titrate with sodium hydroxide standard titration solution [c(NaOH)=0.01 mol/L] until the solution turns yellow, and maintain 305. Add 77.5mL (50g) of sample, shake in a separatory funnel for 3min, and let stand to separate the layers. Separate 50mL of aqueous phase and titrate with sodium hydroxide standard titration solution (Cc (NaOH) = 0.01mol/L) until the solution turns yellow and keep for 30s. The results are calculated according to the provisions of Chapter 7 "Water-insoluble samples" in GB/T 9736. 4.3.4 Benzene Use a 1cm quartz absorption cell and water as a reference to determine the absorbance A of the sample at a wavelength of 255nm. The benzene content is calculated according to the following formula: Where: X—mass percentage of benzene, %, A——absorbance of the sample; 17.6——conversion factor. 4.3.5 Sulfur compounds Measure 3.1mL (2g) of the sample, add 50mL of potassium hydroxide-ethanol solution, and reflux for 30min. Add 50mL of water from the top of the condenser, transfer the sample solution to the evaporator, and evaporate all the organic matter in a water bath. Add 5mL of 30% hydrogen peroxide, keep warm in a water bath for 15min, neutralize with hydrochloric acid solution (20%) and add 1mL in excess, and dilute to 50 mL, and do a blank test at the same time. Take 10mL, evaporate to dryness on a water bath, add 5mL of water to dissolve the residue (filter if necessary), neutralize with sodium hydroxide solution (10g/L), dilute to 20mL, add 0.5mL of hydrochloric acid solution (20%) to acidify, and then determine according to the provisions of GB/T9728. 1156 GB/T 15894—1995 The standard is to take 10mL of blank test solution and impurity standard solution containing 0.06mg sulfate (SO.), dilute to 20mL, and treat the same volume of sample solution at the same time. Determine according to the provisions of GB/T9723, including: 4.3.6.1 Instrument conditions Light source: iron hollow cathode lamp; Wavelength: 248.3nmz Flame: acetylene-air . 4.3.6.2 Determination method Measure 15.5mL (10g) of sample, place in evaporating blood, add 1mL sodium carbonate solution (5g/L), evaporate to dryness on a water bath, dissolve the residue in 5mL nitric acid solution (1+9), dilute to 10mL, and determine according to the provisions of Article 6.2.1 of GB/T9723. 4.3.7 Lead Determine according to the provisions of GB/T9723, including: 4.3.7.1 Instrument conditions| |tt||Light source: lead hollow cathode lamp, wavelength: 283.3nm; flame: acetylene-air. 4.3.7.2 Determination method Same as 4.3.6.2. 4.3.8 Carbonizable substances Measure 10mL of the sample, place it in a dry colorimetric tube, add 10mL of sulfuric acid (super pure, 95.0% ± 0.5%), shake thoroughly (60~70 times/min) )20s, and place for 5min. The color of the acid layer shall not be darker than the standard color Q/8 specified in GB/T9737. 5 Inspection rules Sampling and acceptance shall be carried out in accordance with the provisions of GB/T619. 6 Packaging and marking 6.1 Packaging In accordance with the provisions of HG3-119, among which: Inner packaging form: Xz-4; Outer packaging form: W-1; Packing unit: Class 3 and 4. 6.2 Marking In accordance with the provisions of HG3-119, and indicate "flammable items". 1157 Additional instructions: GB/T15894--1995 This standard is proposed by the Ministry of Chemical Industry of the People's Republic of China. This standard is under the jurisdiction of Beijing Chemical Reagent General Factory. This standard is drafted by Tianjin Chemical Reagent Factory No. 2. The main drafter of this standard is Yan Xiaoyan. From the date of implementation of this standard, the former Ministry of Chemical Industry Standard HG3-1003-76 "Chemical Reagent Petroleum Ether" will be invalid. 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