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HH-THC-30脱活毛细管空柱 HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定

HH-THC-30脱活毛细管空柱 HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定

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产品名称:HH-THC-30脱活毛细管空柱 HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定

产品型号:HH-THC-30脱活毛细管空柱

产品厂商:浩瀚色谱(山东)应用技术开发有限公司

简单介绍

HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定,液化石油气,二甲醚,甲缩醛,乙缩醛,室内空气,焦炉煤气,变压器油,多氯联苯,植物油,6号溶剂残留,顶空进样器

HH-THC-30脱活毛细管空柱 HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定的详细介绍

HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定
HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定 详细信息:

名称:总烃毛细管色谱柱

固定相:脱活的毛细管空柱

规格:30m*0.53mm

型号:HH-THC-30

材质:熔融石英

应用:HJ 38-2017 固定污染源废气 总烃、甲烷和非甲烷总烃的测定 气相色谱法


1 适用范围

      本标准规定了测定固定污染源废气中总烃、甲烷和非甲烷总烃的气相色谱法。

      本标准适用于固定污染源有组织排放废气中的总烃、甲烷和非甲烷总烃的测定。

当进样体积为1.0 ml时,本方法测定总烃、甲烷的检出限均为0.06 mg/m3(以甲烷计),测定下限均为0.24 mg/m3(以甲烷计);非甲烷总烃的检出限为0.07mg/m3(以碳计),测定下限为0.28mg/m3(以碳计)。

2 规范性引用文件

本标准引用了下列文件或其中的条款。凡是不注日期的引用文件,其有效版本适用于本标准。

      GB/T 16157 固定污染源排气中颗粒物测定与气态污染物采样方法

      HJ 732 固定污染源废气挥发性有机物的采样气袋法

      HJ/T 397 固定源废气监测技术规范

3 术语和定义

      下列术语和定义适用于本标准。

3.1

      总烃 total hydrocarbons (THC)

指在本标准规定的测定条件下,在气相色谱仪的氢火焰离子化检测器上有响应的气态有机化合物的总和。

3.2

      非甲烷总烃 nonmethane hydrocarbons (NMHC)

指在本标准规定的测定条件下,从总烃中扣除甲烷以后其他气态有机化合物的总和(除非另有说明,结果以碳计)。

4 方法原理

将气体样品直接注入具氢火焰离子化检测器的气相色谱仪,分别在总烃柱和甲烷柱上测定总烃和甲烷的含量,两者之差即为非甲烷总烃的含量。同时以除烃空气代替样品,测定氧在总烃柱上的响应值,以扣除样品中的氧对总烃测定的干扰。



HJ 38-2017 Waste gas from stationary pollution sources - Determination of total hydrocarbons, methane and non-methane total hydrocarbons
HJ 38-2017 Waste gas from stationary pollution sources - Determination of total hydrocarbons, methane and non-methane total hydrocarbons Details:

Name: Total Hydrocarbon Capillary Column

Stationary phase: deactivated capillary empty column

Specifications: 30m*0.53mm

Model: HH-THC-30

Material: Fused Silica

Application: HJ 38-2017 Waste gas from stationary pollution sources-Determination of total hydrocarbons, methane and non-methane total hydrocarbons-Gas chromatography


1 Scope of application

      This standard specifies the gas chromatography method for the determination of total hydrocarbons, methane and non-methane total hydrocarbons in waste gas from stationary pollution sources.

      This standard is applicable to the determination of total hydrocarbons, methane and non-methane total hydrocarbons in the waste gas of fixed pollution sources.

When the injection volume is 1.0 ml, the detection limit of this method for the determination of total hydrocarbons and methane is 0.06 mg/m3 (calculated as methane), and the lower detection limit is 0.24 mg/m3 (calculated as methane); non-methane total hydrocarbons The detection limit is 0.07mg/m3 (calculated by carbon), and the lower limit of determination is 0.28mg/m3 (calculated by carbon).

2 Normative references

This standard refers to the following documents or clauses thereof. For undated references, the valid edition applies to this standard.

      GB/T 16157 Determination of particulate matter in exhaust gas from stationary pollution sources and sampling methods for gaseous pollutants

      HJ 732 Sampling air bag method for volatile organic compounds in waste gas from stationary pollution sources

      HJ/T 397 Technical Specification for Stationary Source Waste Gas Monitoring

3 Terms and Definitions

      The following terms and definitions apply to this standard.

3.1

      total hydrocarbons (THC)

Refers to the sum of gaseous organic compounds that respond on the hydrogen flame ionization detector of a gas chromatograph under the measurement conditions specified in this standard.

3.2

      nonmethane hydrocarbons (NMHC)

Refers to the sum of other gaseous organic compounds after deducting methane from the total hydrocarbons under the measurement conditions specified in this standard (unless otherwise stated, the results are in carbon terms).

4 Principles of the method

The gas sample was directly injected into a gas chromatograph with a hydrogen flame ionization detector, and the contents of total hydrocarbons and methane were measured on the total hydrocarbon column and the methane column, respectively, and the difference between the two was the content of non-methane total hydrocarbons. At the same time, the sample was replaced by hydrocarbon-removing air, and the response value of oxygen on the total hydrocarbon column was measured to deduct the interference of oxygen in the sample on the determination of total hydrocarbons.

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