E21 原油 标准查询与下载



共找到 182 条与 原油 相关的标准,共 13

本标准规定了海上油田外输原油的品质检验和重量鉴定的程序、方法和要求,包括安全注意事项、输油前检验、输油检验、输油后检验、证书及报告的拟制、分发。 本标准适用于海上油田外输原油的品质检验和重量鉴定。

Rules for inspection and identification of crude oil exported from offshore oilfields

ICS
CCS
E21
发布
2011-05-31
实施
2011-12-01

This test method is one of a number of tests conducted on a crude oil to determine its value. It provides an estimate of the yields of fractions of various boiling ranges and is therefore valuable in technical discussions of a commercial nature. This test method corresponds to the standard laboratory distillation efficiency referred to as 15/5. The fractions produced can be analyzed as produced or combined to produce samples for analytical studies, engineering, and product quality evaluations. The preparation and evaluation of such blends is not part of this test method. This test method can be used as an analytical tool for examination of other petroleum mixtures with the exception of LPG, very light naphthas, and mixtures with initial boiling points above 400°C. 1.1 This test method covers the procedure for the distillation of stabilized crude petroleum (see Note 1) to a final cut temperature of 400°C Atmospheric Equivalent Temperature (AET). This test method employs a fractionating column having an efficiency of 14 to 18 theoretical plates operated at a reflux ratio of 5:1. Performance criteria for the necessary equipment is specified. Some typical examples of acceptable apparatus are presented in schematic form. This test method offers a compromise between efficiency and time in order to facilitate the comparison of distillation data between laboratories. Note 18212;Defined as having a Reid vapor pressure less than 82.7 kPa (12 psi). 1.2 This test method details procedures for the production of a liquefied gas, distillate fractions, and residuum of standardized quality on which analytical data can be obtained, and the determination of yields of the above fractions by both mass and volume. From the preceding information, a graph of temperature versus mass % distilled can be produced. This distillation curve corresponds to a laboratory technique, which is defined at 15/5 (15 theoretical plate column, 5:1 reflux ratio) or TBP (true boiling point). 1.3 This test method can also be applied to any petroleum mixture except liquefied petroleum gases, very light naphthas, and fractions having initial boiling points above 400°C. 1.4 This test method contains the following annexes and appendixes: 1.4.1 Annex A18212;Test Method for the Determination of the Efficiency of a Distillation Column, 1.4.2 Annex A28212;Test Method for the Determination of the Dynamic Holdup of a Distillation Column, 1.4.3 Annex A38212;Test Method for the Determination of the Heat Loss in a Distillation Column (Static Conditions), 1.4.4 Annex A48212;Test Method for the Verification of Temperature Sensor Location, 1.4.5 Annex A58212;Test Method for Determination of the Temperature Response Time, 1.4.6 Annex A68212;Practice for the Calibration of Sensors, 1.4.7 Annex A78212;Test Method for the Verification of Reflux Dividing Valves, 1.4.8 Annex A88212;Practice for Conversion of Observed Vapor Temperature to Atmospheric Equivalent Temperature (AET), 1.4.9 Appendix X18212;Test Method for Dehydration of a Sample of Wet Crude Oil, and 1.4.10 Appendix X28212;Practice for Performance Check. 1.5 The values stated in SI units are to be regarded as the standard. The values given in parentheses......

Standard Test Method for Distillation of Crude Petroleum (15-Theoretical Plate Column)

ICS
75.040 (Crude petroleum)
CCS
E21
发布
2011-01-01
实施

A knowledge of the water content of crude oil is important in the refining, purchase, sale, or transfer of crude oils.1.1 This test method covers the determination of water in the range from 0.02 to 5 mass or volume % in crude oils. Mercaptan (RSH) and sulfide (S− or H2S) as sulfur are known to interfere with this test method, but at levels of less than 500 μg/g (ppm), the interference from these compounds is insignificant (see Section 5). 1.2 This test method can be used to determine water in the 0.005 to 0.02 mass % range, but the effects of the mercaptan and sulfide interference at these levels has not been determined. 1.3 This test method is intended for use with standard commercially available coulometric Karl Fischer reagent. 1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Section 7.

Standard Test Method for Water in Crude Oils by Coulometric Karl Fischer Titration

ICS
75.040 (Crude petroleum)
CCS
E21
发布
2011
实施

This test method is one of a number of tests conducted on a crude oil to determine its value. It provides an estimate of the yields of fractions of various boiling ranges and is therefore valuable in technical discussions of a commercial nature. This test method corresponds to the standard laboratory distillation efficiency referred to as 15/5. The fractions produced can be analyzed as produced or combined to produce samples for analytical studies, engineering, and product quality evaluations. The preparation and evaluation of such blends is not part of this test method. This test method can be used as an analytical tool for examination of other petroleum mixtures with the exception of LPG, very light naphthas, and mixtures with initial boiling points above 400°C. 1.1 This test method covers the procedure for the distillation of stabilized crude petroleum (see Note 1) to a final cut temperature of 400°C Atmospheric Equivalent Temperature (AET). This test method employs a fractionating column having an efficiency of 14 to 18 theoretical plates operated at a reflux ratio of 5:1. Performance criteria for the necessary equipment is specified. Some typical examples of acceptable apparatus are presented in schematic form. This test method offers a compromise between efficiency and time in order to facilitate the comparison of distillation data between laboratories. Note 18212;Defined as having a Reid vapor pressure less than 82.7 kPa (12 psi). 1.2 This test method details procedures for the production of a liquefied gas, distillate fractions, and residuum of standardized quality on which analytical data can be obtained, and the determination of yields of the above fractions by both mass and volume. From the preceding information, a graph of temperature versus mass % distilled can be produced. This distillation curve corresponds to a laboratory technique, which is defined at 15/5 (15 theoretical plate column, 5:1 reflux ratio) or TBP (true boiling point). 1.3 This test method can also be applied to any petroleum mixture except liquefied petroleum gases, very light naphthas, and fractions having initial boiling points above 400°C. 1.4 This test method contains the following annexes and appendixes: 1.4.1 Annex A18212;Test Method for the Determination of the Efficiency of a Distillation Column, 1.4.2 Annex A28212;Test Method for the Determination of the Dynamic Holdup of a Distillation Column, 1.4.3 Annex A38212;Test Method for the Determination of the Heat Loss in a Distillation Column (Static Conditions), 1.4.4 Annex A48212;Test Method for the Verification of Temperature Sensor Location, 1.4.5 Annex A58212;Test Method for Determination of the Temperature Response Time, 1.4.6 Annex A68212;Practice for the Calibration of Sensors, 1.4.7 Annex A78212;Test Method for the Verification of Reflux Dividing Valves, 1.4.8 Annex A88212;Practice for Conversion of Observed Vapor Temperature to Atmospheric Equivalent Temperature (AET), 1.4.9 Appendix X18212;Test Method for Dehydration of a Sample of Wet Crude Oil, and 1.4.10 Appendix X28212;Practice for Performance Check. 1.5 The values stated in SI units are to be regarded as the standard. The values gi......

Standard Test Method for Distillation of Crude Petroleum (15-Theoretical Plate Column)

ICS
75.040 (Crude petroleum)
CCS
E21
发布
2011
实施

Most often determined trace elements in crude oils are nickel and vanadium, which are usually the most abundant; however, as many as 45 elements in crude oils have been reported. Knowledge of trace elements in crude oil is important because they can have an adverse effect on petroleum refining and product quality. These effects can include catalyst poisoning in the refinery and excessive atmospheric emission in combustion of fuels. Trace element concentrations are also useful in correlating production from different wells and horizons in a field. Elements such as iron, arsenic, and lead are catalyst poisons. Vanadium compounds can cause refractory damage in furnaces, and sodium compounds have been found to cause superficial fusion on fire brick. Some organometallic compounds are volatile which can lead to the contamination of distillate fractions, and a reduction in their stability or malfunctions of equipment when they are combusted. The value of crude oil can be determined, in part, by the concentrations of nickel, vanadium, and iron. Inductively coupled plasma-atomic emission spectrometry (ICP-AES) is a widely used technique in the oil industry. Its advantages over traditional atomic absorption spectrometry (AAS) include greater sensitivity, freedom from molecular interferences, wide dynamic range, and multi-element capability. See Practice D7260.1.1 This test method covers the determination of several elements (including iron, nickel, sulfur, and vanadium) occurring in crude oils. 1.2 For analysis of any element using wavelengths below 190 nm, a vacuum or inert gas optical path is required. 1.3 Analysis for elements such as arsenic, selenium, or sulfur in whole crude oil may be difficult by this test method due to the presence of their volatile compounds of these elements in crude oil; but this test method should work for resid samples. 1.4 Because of the particulates present in crude oil samples, if they do not dissolve in the organic solvents used or if they do not get aspirated in the nebulizer, low elemental values may result, particularly for iron and sodium. This can also occur if the elements are associated with water which can drop out of the solution when diluted with solvent. 1.4.1 An alternative in such cases is using Test Method D5708, Procedure B, which involves wet decomposition of the oil sample and measurement by ICP-AES for nickel, vanadium, and iron, or Test Method D5863, Procedure A, which also uses wet acid decomposition and determines vanadium, nickel, iron, and sodium using atomic absorption spectrometry. 1.4.2 From ASTM Interlaboratory Crosscheck Programs (ILCP) on crude oils data available so far, it is not clear that organic solvent dilution techniques would necessarily give lower results than those obtained using acid decomposition techniques. 1.4.3 It is also possible that, particularly in the case of silicon, low results may be obtained irrespective of whether organic dilution or acid decomposition is utilized. Silicones are present as oil field additives and can be lost in ashing. Silicates should be retained but unless hydrofluoric acid or alkali fusion is used for sample dissolution, they may not be accounted for. 1.5 This test method uses oil-soluble metals for calibration and does not purport to quantitatively determine insoluble particulates. Analytical results are particle size dependent and low results may be obtained for particles larger than a few micrometers. 1.6 The precision in Section 18 defines the concentration ranges cover......

Standard Test Method for Multielement Analysis of Crude Oils Using Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES)

ICS
75.040
CCS
E21
发布
2011
实施

The pour point of a crude oil is an index of the lowest temperature of handleability for certain applications. This is the only pour point method specifically designed for crude oils. The maximum and minimum pour point temperatures provide a temperature window where a crude oil, depending on its thermal history, might appear in the liquid as well as the solid state. The test method can be used to supplement other measurements of cold flow behavior. It is especially useful for the screening of the effect of wax interaction modifiers on the flow behavior of crude oils.1.1 This test method covers two procedures for the determination of the pour point temperatures of crude oils down to −36°C. Procedure A provides a measure of the maximum (upper) pour point temperature and is described in 9.1. Procedure B provides a measure of the minimum (lower) pour point temperature and is described in 9.2. 1.2 The use of this test method is limited to use for crude oils. Pour point temperatures of other petroleum products can be determined by Test Method D97. 1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.4 WARNINGMercury has been designated by many regulatory agencies as a hazardous material that can cause central nervous system, kidney and liver damage. Mercury, or its vapor, may be hazardous to health and corrosive to materials. Caution should be taken when handling mercury and mercury containing products. See the applicable product Material Safety Data Sheet (MSDS) for details and EPA’s websitehttp://www.epa.gov/mercury/faq.htmfor additional information. Users should be aware that selling mercury and/or mercury containing products into your state or country may be prohibited by law. 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Section 7.

Standard Test Method for Pour Point of Crude Oils

ICS
75.040 (Crude petroleum)
CCS
E21
发布
2011
实施

Pollution Control Standards for Comprehensive Utilization of Oilfield Oily Sludge

ICS
75.040
CCS
E21
发布
2010-12-28
实施
2011-01-28

SN/T 2418的本部分规定了进口原油的取样、样品处理、品质检验、检验结果的判定。 本部分适用于进口原油管线取样的检验。

Rules for inspection of imported crude oil- Part 2: Pipeline inspection

ICS
CCS
E21
发布
2010-03-02
实施
2010-09-16

SN/T 2418的本部分规定了进口原油的岸罐取样、品质检验、质量检验、检验结果判定、检验报告及安全注意事项。 本部分适用于进口原油岸罐检验。

Rules for inspection of imported crude oil- Part 1: Shore tank inspection

ICS
CCS
E21
发布
2010-03-02
实施
2010-09-16

The emission of mercury during crude oil refining is an environmental concern. The emission of mercury may also contaminate refined products and form amalgams with metals, such as aluminum. When representative test portions are analyzed according to this procedure, the total mercury is representative of concentrations in the sample.1.1 This test method covers the procedure to determine the total mercury content in a sample of crude oil. This test method can be used for total mercury determination in natural and processed liquid and oil products (gasoline, naphtha, etc.). 1.2 This test method may be applied to samples containing between 5.0 to 350 ng/mL of mercury. The results may be converted to mass basis. 1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.4 WARNINGMercury has been designated by many regulatory agencies as a hazardous material that can cause central nervous system, kidney and liver damage. Mercury, or its vapor, may be hazardous to health and corrosive to materials. Caution should be taken when handling mercury and mercury containing products. See the applicable product Material Safety Data Sheet (MSDS) for details and EPA’s websitehttp://www.epa.gov/mercury/faq.htmfor additional information. Users should be aware that selling mercury and/or mercury containing products into your state or country may be prohibited by law. 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 and health practices and determine the applicability of regulatory limitations prior to use.

Standard Test Method for Total Mercury in Crude Oil Using Combustion and Direct Cold Vapor Atomic Absorption Method with Zeeman Background Correction

ICS
75.040
CCS
E21
发布
2010
实施

Vapor pressure of crude oil at various V/Ls is an important physical property for shipping and storage. Note 28212;A vapor-liquid ratio of 0.02:1 (X = 0.02) mimics closely the situation of an oil tanker. Vapor pressure of crude oil is important to crude oil producers and refiners for general handling and initial refinery treatment. The vapor pressure determined by this test method at a vapor-liquid ratio of 4:1 (VPCR4) of crude oil at 37.8°C can be related to the vapor pressure value determined on the same material when tested by Test Method D323 (see Appendix X1). Chilling and air saturation of the sample prior to the vapor pressure measurement is not required. This test method can be applied in online applications in which an air saturation procedure prior to the measurement cannot be performed.1.1 This test method covers the use of automated vapor pressure instruments to determine the vapor pressure exerted in vacuum of crude oils. This test method is suitable for testing samples that exert a vapor pressure between 25 and 180 kPa at 37.8°C at vapor-liquid ratios from 4:1 to 0.02:1 (X = 4 to 0.02). Note 18212;This test method is suitable for the determination of the vapor pressure of crude oils at temperatures from 0 to 100°C and pressures up to 500 kPa, but the precision and bias statements (see Section 14) may not be applicable. 1.2 This test method allows the determination of vapor pressure for crude oil samples having pour points above 0°C. 1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see 7.2.1-7.3.2.

Standard Test Method for Determination of Vapor Pressure of Crude Oil: VPCRx (Expansion Method)

ICS
75.040
CCS
E21
发布
2010
实施

This test method is used to determine the approximate chloride content of crude oils, a knowledge of which is important in deciding whether or not the crude oil needs desalting. The efficiency of the process desalter can also be evaluated. Excessive chloride left in the crude oil frequently results in higher corrosion rates in refining units and also has detrimental effects on catalysts used in these units. This test method provides a rapid and convenient means of determining the approximate content of chlorides in crude oil and is useful to crude oil processors.1.1 This test method covers the determination of the approximate chloride (salts) concentration in crude oil. The range of concentration covered is 0 to 500 mg/kg or 0 to 150 lb/1000 bbl as chloride concentration/volume of crude oil. 1.2 This test method measures conductivity in the crude oil due to the presence of common chlorides, such as sodium, calcium, and magnesium. Other conductive materials may also be present in the crude oil. 1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.3.1 Exception8212;Acceptable concentration units are g/m3 or PTB (lb/1000 bbl). 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific warning statements, see 7.3, 7.4, and 7.11.

Standard Test Method for Salts in Crude Oil (Electrometric Method)

ICS
75.040
CCS
E21
发布
2010
实施

In the absence of water, the crude oil is noncorrosive. The presence of sediment and water makes crude oil corrosive. Test Methods , , , and provide methods for the determination of the water and sediment content of crude oil. The corrosivity of crude oil containing water can be determined by a combination of three properties (Fig. 1) (1) : the type of emulsion formed between oil and water, the wettability of the steel surface, and the corrosivity of water phase in the presence of oil. Water and oil are immiscible but, under certain conditions, they can form emulsion. There are two kinds of emulsion: O/W and W/O. W/O emulsion (in which oil is the continuous phase) has low conductivity and is thus less corrosive; whereas O/W (in which water is the continuous phase) has high conductivity and, hence, is corrosive (see ISO 6614) (2). The conductivities of various liquids are provided in Table 1(3). The percentage of water at which W/O converts to O/W is known as the emulsion inversion point (EIP). EIP can be determined by measuring the conductivity of the emulsion. At and above the EIP, a continuous phase of water or free water is present. Therefore, there is a potential for corrosion. Whether water phase can cause corrosion in the presence of oil depends on whether the surface is oil wet (hydrophobic) or water wet (hydrophilic) (4-8). Because of higher resistance, an oil-wet surface is not susceptible to corrosion, but a water-wet surface is. Wettability can be characterized by measuring the contact angle or the conductivity (spreading method). In the contact angle method, the tendency of water to displace hydrocarbon from steel is measured directly by observing the behavior of the three phase system. The contact angle is determined by the surface tensions (surface free energies) of the three phases. A hydrocarbon-steel interface will be replaced by a water-steel interface if this action will result in an energy decrease of the system. To determine whether the surface is oil wet, mixed wet, or water wet, the angle at the oil-water-solid intersection is observed and measured. In the spreading method of determining wettability, the resistance between steel pins is measured. If a conducting phase (for example, water) covers (wets) the distance between the pins, conductivity between them will be high. On the other hand, if a nonconducting phase (for example, oil) covers (wets) the distance between the pins, the conductivity between them will be low. Dissolution of ingredients from crude oils may alter the corrosiveness of the aqueous phase. Based on how the corrosivity of the aqueous phase changes in its presence, a crude oil can be classified as corrosive, neutral, inhibitory, or preventive crude. Corrosiveness of the aqueous phase in the presence of oil can be determined by methods described in Test Method , Guide , Practice , Test Method , and NACE TM0172.1.1 This guide presents some generally accepted laboratory methodologies that are used for determining the corrosivity of crude oil. 1.2 This guide does not cover detailed calculations and methods, but rather a range of approaches that have found application in evaluating the corrosivity of crude oil. 1.3 Only those methodologies that have found wide acceptance in crude oil corrosivity evaluation are considered in this guide. 1.4 This guide does not address the change in oil/water ratio caused by accumulation of water at low points in a pipeline system. 1.5 This guide is intended to assist in the selection of methodologies that can be used for determining the corrosivity of crude oil under conditions in which water is present in the liquid state (typically up to 100°C). These conditions nor......

Standard Guide for Determining Corrosivity of Crude Oils

ICS
75.040
CCS
E21
发布
2010
实施

This test method is one of a number of tests conducted on a crude oil to determine its value. It provides an estimate of the yields of fractions of various boiling ranges and is therefore valuable in technical discussions of a commercial nature. This test method corresponds to the standard laboratory distillation efficiency referred to as 15/5. The fractions produced can be analyzed as produced or combined to produce samples for analytical studies, engineering, and product quality evaluations. The preparation and evaluation of such blends is not part of this test method. This test method can be used as an analytical tool for examination of other petroleum mixtures with the exception of LPG, very light naphthas, and mixtures with initial boiling points above 400°C. 1.1 This test method covers the procedure for the distillation of stabilized crude petroleum (see Note 1) to a final cut temperature of 400°C Atmospheric Equivalent Temperature (AET). This test method employs a fractionating column having an efficiency of 14 to 18 theoretical plates operated at a reflux ratio of 5:1. Performance criteria for the necessary equipment is specified. Some typical examples of acceptable apparatus are presented in schematic form. This test method offers a compromise between efficiency and time in order to facilitate the comparison of distillation data between laboratories. Note 18212;Defined as having a Reid vapor pressure less than 82.7 kPa (12 psi). 1.2 This test method details procedures for the production of a liquefied gas, distillate fractions, and residuum of standardized quality on which analytical data can be obtained, and the determination of yields of the above fractions by both mass and volume. From the preceding information, a graph of temperature versus mass % distilled can be produced. This distillation curve corresponds to a laboratory technique, which is defined at 15/5 (15 theoretical plate column, 5:1 reflux ratio) or TBP (true boiling point). 1.3 This test method can also be applied to any petroleum mixture except liquefied petroleum gases, very light naphthas, and fractions having initial boiling points above 400°C.

Standard Test Method for Distillation of Crude Petroleum (15-Theoretical Plate Column)

ICS
75.040
CCS
E21
发布
2010
实施

本标准规定了稳定轻烃取样时使用的仪器、取样步骤、取样记录和安全注意事项。 本标准适用于油气田稳定轻烃的取样。 警告:使用本标准的人员应有正规实验室工作的实践经验。本标准并未指出所有可能的安全问题。使用者有责任采取适当的安全和健康措施,并保证符合国家有关规定条件。

Sampling method of natureal gasoline

ICS
75.040
CCS
E21
发布
2009-12-01
实施
2010-05-01

本标准规定了原油凝点的测定法。 本标准适用于含水质量分数不超过0.5%的原油。 警告:使用本标准的人员应有正规实验室工作的实践经验。本标准并未指出所有可能的安全问题。使用者有责任采取适当的安全和健康措施,并保证符合国家有关规定条件。

Test method for gel point of crude oils

ICS
75.040
CCS
E21
发布
2009-12-01
实施
2010-05-01

The pour point of a crude oil is an index of the lowest temperature of handleability for certain applications. This is the only pour point method specifically designed for crude oils. The maximum and minimum pour point temperatures provide a temperature window where a crude oil, depending on its thermal history, might appear in the liquid as well as the solid state. The test method can be used to supplement other measurements of cold flow behavior. It is especially useful for the screening of the effect of wax interaction modifiers on the flow behavior of crude oils.1.1 This test method covers two procedures for the determination of the pour point temperatures of crude oils down to −36°C. Procedure A provides a measure of the maximum (upper) pour point temperature and is described in 9.1. Procedure B provides a measure of the minimum (lower) pour point temperature and is described in 9.2. 1.2 The use of this test method is limited to use for crude oils. Pour point temperatures of other petroleum products can be determined by Test Method D 97. 1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 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 and health practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see Section 7.

Standard Test Method for Pour Point of Crude Oils

ICS
75.040 (Crude petroleum)
CCS
E21
发布
2009
实施

Methanol is used in production of crude oil to prevent formation of gas hydrates. The presence of residual methanol in crude oils can lead to costly problems in refinery operations.1.1 This test method covers the determination of methanol in crude oils by direct injection multidimensional gas chromatography in the concentration range of 15 to 900 ppm (m/m). The pooled limit of quantification (PLOQ) is 15 ppm (m/m). 1.2 This test method is applicable only to crude oils containing less than or equal to 0.1 % (v/v) water. 1.3 This test method has not been tested with crude oil samples that are solid or waxy, or both, at ambient temperatures. 1.4 The values stated in SI units are to be regarded as standard. Alternate units, in common usage, are also provided to increase clarity and aid the users of this test method. 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 and health practices and determine the applicability of regulatory limitations prior to use.

Standard Test Method for Determination of Methanol in Crude Oils by Multidimensional Gas Chromatography

ICS
75.040 (Crude petroleum)
CCS
E21
发布
2009
实施

本标准规定了用气相色谱法分析原油中正辛烷及以前烃组分的方法、试剂材料、仪器设备、取样方法、操作步骤、定性定量方法、精密度。 本标准适用于测定原油中正辛烷及以前烃组分的含量,对含水原油指均相乳状液原油。

Determination of octane and hydrocarbon components before octane in crude petroleum.Gas chromatography

ICS
75.040
CCS
E21
发布
2008-06-16
实施
2008-12-01

本标准规定了测定原油含水量的电脱法所用的仪器、试剂、操作步骤方法以及分析结果的计算与重复性。 本标准适用于油田采油生产过程中5%以上含水原油的含水量的测定。

Crude petoleum determination of water.Electric dehydration method

ICS
75.040
CCS
E21
发布
2008-06-16
实施
2008-12-01



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