75.080 石油产品综合 标准查询与下载

ISO 3838:2004/DAmd 1 原油和液体或固体石油产品密度或相对密度的测定毛细管塞比重瓶和刻度双毛细管比重瓶方法修正案1

Crude petroleum and liquid or solid petroleum products — Determination of density or relative density — Capillary-stoppered pyknometer and graduated bicapillary pyknometer methods — Amendment 1

ISO/FDIS 3104:2023 石油产品 透明和不透明液体 运动粘度的测定和动力粘度的计算

Petroleum products — Transparent and opaque liquids — Determination of kinematic viscosity and calculation of dynamic viscosity

T/DYZL 032-2023 东营市成品油质量检验检测异常数据处置规范

本文件主要规定了东营市成品油可追溯平台企业检验检测数据研究法辛烷值阈值、两实验室间硫含量检验检测数据阈值、两实验室间密度(20℃)检验检测数据阈值、两实验室间十六烷值检验检测数据阈值范围

Dongying City Product Oil Quality Traceability Management Platform Inspection and Detection Abnormal Data Analysis and Disposal Specification

23/30463813 DC BS EN ISO 18335 石油产品及相关产品 通过计算测得的动态粘度和密度来确定运动粘度 恒压粘度计法

BS EN ISO 18335. Petroleum products and related products. Determination of kinematic viscosity by calculation from the measured dynamic viscosity and density. Method by constant pressure viscometer

ISO/TS 23877-1:2023 天然或合成来源的石油及相关产品倾点的测定第1部分：自动逐步冷却方法

Petroleum and related products from natural or synthetic sources — Determination of pour point — Part 1: Automated step-wise cooling method

ASTM D1552-23 通过高温燃烧和红外（IR）检测或热导检测（TCD）检测石油产品中硫的标准测试方法

1.1  This test method covers procedures for the determination of total sulfur in petroleum products including lubricating oils containing additives, and in additive concentrates. This test method is applicable to samples boiling above 177 °C (350 °F). Other sulfur concentrations outside of those listed in 1.1.1 and 1.1.2 may be analyzed, but the precision stated may or may not apply. These procedures use IR detection or TCD following combustion in a furnace. 1.1.1  Procedure A, IR Detection:  1.1.1.1  This procedure is applicable to samples containing a mass fraction of sulfur between 0.22 % and 24.2 %. 1.1.1.2  Petroleum coke containing a mass fraction of sulfur between 2.53 % to 3.79 % sulfur may be analyzed. 1.1.2  Procedure B, TCD Detection:  1.1.2.1  This procedure is applicable to samples containing a mass fraction of sulfur between 0.071 % and 25.8 %. 1.1.2.2  Petroleum coke containing a mass fraction of sulfur between 0.19 % to 6.38 % sulfur may be analyzed. 1.2  Petroleum coke containing a mass fraction of sulfur between 2.53 % to 3.79 % sulfur may be analyzed. Other sulfur concentrations may be analyzed, but the precision stated may or may not apply. Note 1:  The D1552  – 08 (2014) version of this standard contained two other procedures using iodate titrations. Since these procedures are no longer being used in the industry laboratories based on a survey of D02.SC 3 laboratories conducted in September 2014, they are being deleted. For earlier information on the deleted procedures, D1552  – 08 (2014) may be perused. 1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only. 1.4  This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.5  This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Standard Test Method for Sulfur in Petroleum Products by High Temperature Combustion and Infrared (IR) Detection or Thermal Conductivity Detection (TCD)

KS M 2459-1-2023 石油产品和相关产品.水性石油中油源识别的测定.第1部分:气相色谱火焰离子化检测器（GC-FID）

Petroleum products and related products — Determination of oil source identification in waterborne petroleum oil — Part 1: Gas chromatograph-flame ionization detector (GC-FID)

GSO ISO 22854:2023 液态石油产品 车用汽油和乙醇（E85）车用燃料中烃类和含氧化合物的测定 多维气相色谱法

This document specifies the gas chromatographic (GC) method for the determination of saturated, olefinic and aromatic hydrocarbons in automotive motor gasoline and ethanol (E85) automotive fuel. Additionally, the benzene and toluene content, oxygenated compounds and the total oxygen content can be determined. NOTE 1   For the purposes of this document, the terms % (m/m) and % (V/V) are used to represent respectively the mass fraction, w, and the volume fraction, φ. This document defines two procedures, A and B. Procedure A is applicable to automotive motor gasoline with total aromatics of 19,32 % (V/V) up to 46,29 % (V/V); total olefins from 0,40 % (V/V) up to 26,85 % (V/V); oxygenates from 0,61 % (V/V) up to 9,85 % (V/V); oxygen content from 1,50 % (m/m) to 12,32 % (m/m); benzene content from 0,38 % (V/V) up to 1,98 % (V/V) and toluene content from 5,85 % (V/V) up to 31,65 % (V/V). The method has also been tested for individual oxygenates. A precision has been determined for a total volume of methanol from 1,05 % (V/V) up to 16,96 % (V/V); a total volume of ethanol from 0,50 % (V/V) up to 17,86 % (V/V); a total volume of MTBE from 0,99 % (V/V) up to 15,70 % (V/V), a total volume of ETBE from 0,99 % (V/V) up to 15,49 % (V/V), a total volume of TAME from 0,99 % (V/V) up to 5,92 % (V/V), and a total volume of TAEE from 0,98 % (V/V) up to 15,59 % (V/V). Although this test method can be used to determine higher-olefin contents of up to 50 % (V/V), the precision for olefins was tested only in the range from 0,40 % (V/V) to 26,85 % (V/V). Although specifically developed for the analysis of automotive motor gasoline that contains oxygenates, this test method can also be applied to other hydrocarbon streams having similar boiling ranges, such as naphthas and reformates. NOTE 2   For Procedure A, applicability of this document has also been verified for the determination of n-propanol, acetone, and di-isopropyl ether (DIPE). However, no precision data have been determined for these compounds. Procedure B describes the analysis of oxygenated groups (ethanol, methanol, ethers, C3 – C5 alcohols) in ethanol (E85) automotive fuel containing ethanol between 50 % (V/V) and 85 % (V/V). The gasoline is diluted with an oxygenate-free component to lower the ethanol content to a value below 20 % (V/V) before the analysis by GC. The sample can be fully analysed including hydrocarbons. Precision data for the diluted sample are only available for the oxygenated groups. NOTE 3   For Procedure B, the precision can be used for an ethanol fraction from about 50 % up to 85 % (V/V). For the ether fraction, the precision as specified in Table 6 can be used for samples containing at least 11 % (V/V) of ethers. For the higher alcohol fraction, too few data were obtained to derive a full precision statement and the data presented in Table 6 are therefore only indicative. NOTE 4   An overlap between C9 and C10 aromatics can occur. However, the total is accurate. Isopropyl benzene is resolved from the C8 aromatics and is included with the other C9 aromatics.

Liquid petroleum products — Determination of hydrocarbon types and oxygenates in automotive-motor gasoline and in ethanol (E85) automotive fuel — Multidimensional gas chromatography method

GSO ASTM D5772:2023 石油产品和液体燃料浊点的标准测试方法（线性冷却速率法）

  Scope is not provided for this standard

Standard Test Method for Cloud Point of Petroleum Products and Liquid Fuels (Linear Cooling Rate Method)

GSO ISO 3104:2023 石油产品 透明和不透明液体 运动粘度的测定和动力粘度的计算

This document specifies Procedure A, using manual glass viscometers, and Procedure B, using glass capillary viscometers in an automated assembly, for the determination of the kinematic viscosity, ν, of liquid petroleum products, both transparent and opaque, by measuring the time for a volume of liquid to flow under gravity through a calibrated glass capillary viscometer. The dynamic viscosity, η, is obtained by multiplying the measured kinematic viscosity by the density, ρ, of the liquid. The range of kinematic viscosities covered in this test method is from 0,2 mm2/s to 300 000 mm2/s over the temperature range ?20 °C to +150 °C. NOTE The result obtained from this document is dependent upon the behaviour of the sample and is intended for application to liquids for which primarily the shear stress and shear rates are proportional (Newtonian flow behaviour). If, however, the viscosity varies significantly with the rate of shear, different results can be obtained from viscometers of different capillary diameters. The procedure and precision values for residual fuel oils, which under some conditions exhibit non-Newtonian behaviour, have been included.

Petroleum products — Transparent and opaque liquids — Determination of kinematic viscosity and calculation of dynamic viscosity

GSO ASTM D129:2023 石油产品中硫的标准测试方法（通用高压分解装置方法）

This standard details the general bomb test method for determination of the amount of sulfur in lubricating oils with additives, additive concentrates, lubricating greases, and other petroleum products with low volatilities. This test method entails oxidizing samples by combustion in a bomb containing oxygen under pressure. The amount of sulfur is determined by gravimetry. Materials needed for the test include a combustion bomb, sample cup, firing wire, ignition circuit, and a cotton wicking or nylon sewing thread. All reagents, samples, and other chemicals used for the test should conform to the required concentration and purity.

Standard Test Method for Sulfur in Petroleum Products (General High Pressure Decomposition Device Method)

GSO ISO 14935:2023 石油及相关产品 耐火液体灯芯火焰持久性的测定

This document specifies a method for the assessment of the persistence of a flame applied to the edge of a wick of non-flammable material immersed in fire-resistant fluid. This test does not determine the behaviour of a spray of fire-resistant fluid. NOTE Such test methods are specified in ISO 15029-1 and ISO 15029-2. This document specifies one of four basic tests for determining flammability. This document does not apply to certain liquids such as HFAE and HFAS liquids.

Petroleum and related products — Determination of wick flame persistence of fire-resistant fluids

GSO ASTM D4177:2023 石油和石油产品自动取样的标准实施规程

This practice describes general procedures and equipment for automatically obtaining samples of liquid petroleum and petroleum products, crude oils, and intermediate products from the sample point into the primary container. This practice also provides additional specific information about sample container selection, preparation, and sample handling. If sampling is for the precise determination of volatility, use Practice D5842 (API MPMS Chapter 8.4) in conjunction with this practice. For sample mixing and handling, refer to Practice D5854 (API MPMS Chapter 8.3). This practice does not cover sampling of electrical insulating oils and hydraulic fluids.

Standard Practice for Automatic Sampling of Petroleum and Petroleum Products

GSO ISO 13736:2023 闪点的测定 阿贝尔闭杯法

This document specifies a method for the determination of the manual and automated closed cup flash point of combustible liquids having flash points between –30,0 °C to 75,0 °C. However, the precision given for this method is only valid for flash points in the range −8,5 °C to 75,0 °C. This document is not applicable to water-borne paints. NOTE 1   Water borne paints can be tested using ISO 3679[1]. NOTE 2   See 9.1 for the importance of this test in avoiding loss of volatile materials. NOTE 3   Liquids containing halogenated compounds can give anomalous results. NOTE 4   The thermometer specified for the manual apparatus limits the upper test temperature to 70,0 °C. NOTE 5   See 13.1 for more specific information related to precision.

Determination of flash point — Abel closed-cup method

GSO ISO 2592:2023 石油及相关产品 闪点和燃点的测定 克利夫兰开杯法

ISO 2592:2017 specifies a procedure for the determination of flash and fire points of petroleum products using the Cleveland open cup apparatus. It is applicable to petroleum products having open cup flash points between 79 °C and 400 °C, except fuel oils which are most commonly tested by the closed cup procedure described in ISO 2719.

Petroleum and related products — Determination of flash and fire points — Cleveland open cup method

GSO ISO/TR 29662:2023 石油产品和其他液体闪点和可燃性测试指南

This document establishes an overview of test methods in the field to determine flash point and combustibility of petroleum and related products. It presents advice on application and specification development. This document is not intended to be a comprehensive manual on flash point and combustibility tests, and the interpretation of test results, however it covers the key aspects on these subjects.

Petroleum products and other liquids — Guidance for flash point and combustibility testing

GSO ASTM D7260:2023 用于石油产品和润滑油元素分析的电感耦合等离子体原子发射光谱法 (ICP-AES) 的优化、校准和验证的标准实施规程

  Scope is not provided for this standard

Standard Practice for Optimization, Calibration, and Validation of Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) for Elemental Analysis of Petroleum Products and Lubricants

ASTM D2008-23 石油产品紫外线吸收率和吸收率的标准试验方法

1.1 This test method covers the measurement of the ultraviolet absorption of a variety of petroleum products. It covers the absorbance of liquids or the absorptivity of liquids and solids, or both, at wavelengths in the region from 220 nm to 400 nm of the spectrum. 1.2 The use of this test method implies that the conditions of measurement—wavelength, solvent (if any), sample path length, and sample concentration—are specified by reference to one of the examples of the application of this test method in the annexes or by a statement of other conditions of measurement. 1.3 Examples of the application of this test method are the absorptivity of refined petroleum wax, and the absorptivity of USP petrolatum. 1.4 The values stated in SI units are to be regarded as the standard. The values stated in Fahrenheit, feet, and inches, indicated in parentheses, are for information only. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see 7.3.1, 7.3.3, and 13.4. 1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Standard Test Method for Ultraviolet Absorbance and Absorptivity of Petroleum Products

BS EN 15522-2:2023 溢油识别 石油及石油相关产品 基于 GC-FID 和 GC-低分辨率-MS 分析的分析方法和结果解释

1   Scope This document specifies a method to identify and compare the compositional characteristics of oil samples. Specifically, it describes the detailed analytical and data processing methods for identifying the characteristics of spill samples and establishing their correlation to suspected source oils. Even when samples or data from suspected sources are not available for comparison, establishing the specific nature (e.g. refined petroleum, crude oil, waste oil, etc.) of the spilled oil still helps to constrain the possible source(s). This methodology is restricted to petroleum related products containing a significant proportion of hydrocarbon-components with a boiling point above 150 °C. Examples are: crude oils, higher boiling condensates, diesel oils, residual bunker or heavy fuel oils, lubricants, and mixtures of bilge and sludge samples, as well as distillate fuels and blends. While the specific analytical methods are perhaps not appropriate for lower boiling oils (e.g. kerosene, jet fuel, or gasoline), the general concepts described in this methodology, i.e. statistical comparison of weathering -resistant diagnostic ratios , are applicable in spills involving these kinds of oils. Paraffin products (e.g. waxes, etc.) are outside the scope of this method because too many compounds are removed during the production process [37] to correctly distinguish them from each other. However, the method can be used to identify the type of product involved. Although not directly intended for identifying oil recovered from groundwater, vegetation, wildlife/tissues,...

Oil spill identification. Petroleum and petroleum related products. Analytical method and interpretation of results based on GC-FID and GC-low resolution-MS analyses

ASTM D6792-23a 石油产品、液体燃料和润滑剂试验实验室质量管理体系的标准实施规程

1.1 This practice covers the establishment and maintenance of the essentials of a quality management system in laboratories engaged in the analysis of petroleum products, liquid fuels, and lubricants. It is designed to be used in conjunction with Practice D6299. NOTE 1—This practice is based on the quality management concepts and principles advocated in ANSI/ISO/ASQ Q9000 standards, ISO/IEC 17025, ASQ Manual,2 and ASTM standards such as D3244, D4182, D4621, D6299, D6300, D7372, E29, E177, E456, E548, E882, E994, E1301, E1323, STP 15D,3 and STP 1209.4 1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory requirements prior to use. 1.3 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Standard Practice for Quality Management Systems in Petroleum Products, Liquid Fuels, and Lubricants Testing Laboratories