氢氧化钠吸收液-离子色谱法测固定污染源废气中的氯气

建立了氢氧化钠吸收液-离子色谱测定固定污染源废气中氯气的方法。研究采样和分析条件,采用50 mL冲击式吸收瓶,以氢氧化钠为吸收液,利用硫代硫酸钠将样品中的次氯酸完全转化为氯离子,过滤后用离子色谱进行分析。可在采样时选择0.3 μm石英滤膜消除颗粒物干扰,在氢氧化钠吸收液前串联硫酸吸收液消除氯化氢干扰。测试结果显示:氯离子曲线线性关系良好,相关系数为0.999 0;方法检出限为0.02 mg/m³,测定下限为0.08 mg/m³;空白加标的相对标准偏差为0.82%~1.4%,加标回收率为98.0%~107%;实际样品基体加标的相对标准偏差为1.8%~2.7%,加标回收率为98.0%~104%。测试结果表明该方法具有较高的精密度和正确度。     

气相色谱法测定废水中的茚及芳烃混合物

本文采用气相色谱法,选择中等极性的Ｔｒｉｃｒｅｓｙｌｐｈｏｓｐｈａｔｅ与高沸点的非极性ＡｐｉｅｚｏｎＬ配成混合固定液,测定工业废水中的茚及芳烃混合物。该方法灵敏度高,再现性好,简便快速,适合测定化工、制漆、制茚树脂生产所排放的废水,同时也能检出受苯系物及高沸点的不饱合物萘等多组分污染的水体     

气相色谱法测定水和废水中丙烯腈

本文通过采用气相色谱法,以ＧＤＸ－５０２为固定相,ＦＩＤ为检测器测定水和废水中的丙烯腈,精密度和回收率高．方法简便易行,能满足行业废水和地面水的监队是水和废水中丙烯腈分析的较理想方法。     

气相色谱法测定水和气体样品中的二硫化碳

本文研究了用气相色谱电子捕获检测器测定水和气体样品中二硫化碳的方法。本方法采取顶空进样法测水质样品,直接进样测气体样品。色谱柱为ＧＤＸ—１０１填充柱。方法简单,灵敏度高,水质样品最低检出浓度可达００００５ｍｇ／Ｌ,气体样品最低检出浓度达０００５ｍｇ／ｍ３。方法的精密度为５７％,回收率为９０３％。     

GC-PID联用直接测定大气中痕量烃类化合物

作者把气相色谱仪(GC)与自行研制的光离子化检测器(PID)联用,实现了大气中痕量烃类化合物的直接测定,给出了仪器的构成和性能指标及测量结果.     

顶空气相色谱法测定土壤中BTEX

本文采用顶空气相色谱法从土壤样品中分离挥发性有机物。应用该技术,苯、甲苯、乙基苯及二甲苯异构体（ＢＴＥＸ）均得到有效分离。该方法有较好的精密度（变异系数６５％,回收率８９～１０３％）和低的检出限（对于苯为０５ｎｇ／ｇ）。土壤样品中加入水或加热,可提高方法的灵敏度。     

大气中酮类化合物污染事故应急监测

研究了大气中低分子量酮类化合物的气相色谱测定方法 ,进行了线性范围、精密度和准确度实验。结果表明 ,该方法具有简便快捷、准确灵敏的特点 ,适合于大气污染事故应急监测     

Variation in some chemical parameters and organic matter in soils regenerated by the addition of municipal solid waste

The organic fraction of a municipal solid waste was added in different doses to an eroded soil formed of loam and with no vegetal cover. After three years, the changes in macronutrient content and the chemical-structural composition of its organic matter were studied. The addition of the organic fraction from a municipal solid waste had a positive effect on soil regeneration, the treated soils being covered with spontaneous vegetation from 1 yr onwards. An increase in electrical conductivity and a fall in pH were noted in the treated soils as were increases in macronutrients, particularly N and available P and the different carbon fractions. Optical density measurements of the organic matter extracted with sodium pyrophosphate showed that the treated soils contained an organic matter with less condensed compounds and with a greater tendency to evolve than the control. A pyrolysis-gas chromatography study of the organic matter extracted with pyrophosphate showed large quantities of benzene both in the treated soils and control; pyrrole was also relatively abundant, although this fragment decreased as the dose rose. Xylenes and pyridine were present in greater quantities in the control and furfural in the treated soils. Three years after addition to the soil, the organic matter had a higher proportion of fragments derived from aromatic compounds and a smaller proportion derived from hydrocarbons. Similarity indices showed that, although the added and newly formed organic matter 3 yr after addition continued to differ from that of the original soil and to be more mineralizable, the transformations it has undergone made it more similar to the original organic matter of the soil than it was at the moment of being added.     

环境样品中PCBs的测定

详细地介绍了应用ＧＣ／ＭＳ或ＧＣ／ＥＣＤ测定样品的ＰＣＢｓ的分析方法及榈前处理的方法，并给出了３０个行政检查样品的测定结果。     

Analysis of organic compounds in coal gasification wastewater

A procedure for analysis of organic pollutants in coal gasification wastewater was developed, including a series extraction steps at different pH, followed by LC separation or resin adsorption, then analyzed by GC or GC/MS. More than 200 organic pollutants in 22 categories were determined. CH2CL2 extraction at NaHCO3 presence was used to separate carboxylic acids with phenolic compounds in aqueous. Derivatization with acetic anhydride was used for analyses of mono-, di-, poly-hydroxyl phenolic compounds. 21 mono-hydroxyl phenols and 13 di-hydroxyl phenols were determined from the coai gasification wastewater samples. Derivatization with BF3-CH3OH was used for analysis of carboxylic acid. 17 mono-carboxyl, 4 di-carboxyl acids and 6 aromatic acids were determined from coal gasification wastewater samples.