环境中N，N──二甲基甲酰胺的气相色谱分析

本法采用直接注入水溶液样品,方法适应性强,水、气均可分析,浓度在１～１００ｍｇ／Ｌ范围内的线性良好,相关系数０．９９９以上。灵敏度高,相对标准偏差小于４％,最低检测浓度为ｌ．ｏｍｇ／Ｌ,回收率均在９５％～１０５％之间。     

催化分光光度法测定痕量Fe(Ⅲ)

基于在HCl介质中，Fe（Ⅲ）强烈地催化H2O2氧化次甲基绿的反应，建立了测定超痕量Fe（Ⅲ）的新方法。方法检出限为0．005μg/L，测定范围为0－0．25mg/L。本法对地下饮用水、人发、环境标准样品进行了测定。     

氢化物发生—原子荧光法测定水中痕量铅

以过硫酸铵为氧化剂将铅氧化成亚稳四价态,与ＫＢＨ４作用生成ＰｂＨ４,应用氢化物发生—原子荧光测定水中痕量铅。本法灵敏度较高,检测限为０．６８μｇ／Ｌ;其回收率在９０—１０５％之间;变异系数为２．１—３．４％。     

微波消解-石墨炉原子吸收法测定小麦中钴

利用微波消解-石墨炉原子吸收法检测小麦样品中的低含量钴,方法简单、操作便捷,测定结果精确度和准确度好。钴的线性回归方程为A=0．003303c＋0．004218,测定结果的相对标准偏差为4．1％（标准样品ESP-1）和1．1％（6#小麦样品）,检出限为0．005mdkg。     

改进后的差示光度法分析低浓度挥发酚

应用差示光度法的有关原理及朗伯比耳定律的最佳适用范围,在光度计测量误差较小的最佳测量范围内测量样品的吸光值。结果表明对地表水挥发酚的检测,本法与４－氨基安替比林（４ＡＡＰ）萃取光度法相比准确度达到９５％,精密度良好。     

无汞开管法快速测定工业废水中的COD

采用无汞开管法测定 COD。方法使用硫酸 -磷酸介质、重铬酸钾氧化体系 ,以硫酸银作催化剂 ,其他试剂包括硝酸银和硫酸铬钾以排除氯离子的干扰。样品在玻璃试管中进行消化 ,用一台恒温器加热样品 ,反应温度 1 65℃ ,加热时间只需 1 0 min,消解后剩余的重铬酸盐用分光光度法或滴定法测定。试验结果表明 ,本法的检出限为 1 0 .9mg/ L,测定范围为 3 0～ 1 5 0 0 mg/ L。由于方法不使用剧毒的汞盐 ,也就避免了汞对环境的污染。应用本法测定了大批量工业废水样品 ,结果令人满意     

皮革铬鞣废水回收利用中铬渣的铬量测定

本文研究了皮革铬鞣废水中铬的定性特征曲线。利用吸光度加合定律对大量实测数据进行统计处理。建立测定铬的实验室校准直线方程,相关系数γ＝０．９９６０．以此作为测定铬鞣废水及回收铬渣中铬量的实验室回归直线方程。并对本法的可靠性进行研究,结果令人满意。本法不仅大大简化了铬量测定的步骤．而且在提高分析效率的同时获得同等的检测结果。     

丙酮、苯、甲苯、二甲苯、乙苯、苯乙烯的分析(气相色谱法)

本法分析高含量车间气体样品时(大于100mg/m~3),分析结果的变异系数范围为2％左右。分析低含量大气样品时(小于1mg/m~3),其分析结果的变异系数范围为4～11％,方法对高含量环境样品的加标回收率范围为90～97％。对低含量大气样品的加标回收率范围78～112％。     

离子色谱法测定水中F~－，Cl~－，NO_3~－和SO_4~(2－)的实践

报导了用离子色谱法同时测定水中Ｆ~－，Ｃｌ~－、ＮＯ_3~－和ＳＯ_4~（2－）的最佳分析条件；研究了各组分测定的精密度，准确度，检测限和线性范围。用本法分析样品，获得了满意的结果。     

荧光分光光度法测定大气飘尘中的硒

本法对美国《空气采样与分析方法》中介绍的用荧光分光光度法测定大气颗粒物中硒的方法进行了较大的改进。将采集来的滤膜样品用硝酸氧化,在pH_2的酸性溶液中与2,3—二氨基萘反应,采用沸水浴加热,缩短了反应时间,用环已烷作萃取剂,提高了灵敏度。对于金属干扰离子则用国产732~#阳离子交换树脂进行分离。本法的线性范围为0.01～0.4μg,最低检测限为0.0012μg,当采样体积为20m~3时,最低检出浓度为0.0005μg/m~3。精密度为2.7％,回收率在92％～100％之间,适用于一般大气飘尘中硒的测定。     

副玫瑰苯胺无汞比色法测定空气中的甲醛

在甲醛法测定空气中二氧化硫的基础上,建立了一种测定空气中甲醛的新方法。该方法所用设备和材料与甲醛法测定空气中的二氧化硫相同,不使用含汞试剂,用亚硫酸钠固定标准溶液和吸收液中的甲醛,用氢氧化钠分解羟甲磺酸释放已被固定的甲醛,以副玫瑰苯胺和亚硫酸钠为显色剂绘制标准曲线进行定量。当采集空气30L时,检出限为0.01mgm3,最低检测浓度为0.03mgm3,适用于环境空气及室内空气中甲醛的测定。     

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％。     

Effect Of Reagent (Dye) Addition In Wet Chemical Method Of Sulfur Dioxide Determination In Ambient Air

For measurement of sulfur dioxide (SO₂) in ambient air, the United States Environment Protection Agency (US EPA) had recommended the PRA dye-based colorimetric method as a reference technique. The method has been developed and applied in many countries for a longtime; however information regarding the sensitivity of the method with respect to sampling and analysis conditions is not available. Collaborative studies conducted in some of the South East Asian countries indicated substantial variations (of the order of 50%) in the measured concentrations against the true values. It was observed that dye used for color development plays an important role and even a slight variation in the way the dye solution is prepared can cause substantial variation in the measured SO₂ concentration. Because a major objective of air quality measurements is to relate air pollution concentration to the effects of air pollution, it is important that the method used should yield accurate levels of the pollutant, so that appropriate management plans can be devised and implemented effectively. In the present investigation, therefore, the role of dye used in SO₂ monitoring method has been highlighted. Different makes of dyes prepared in different modes were used to study the variation in the measured SO₂ concentration levels. Specifications of all the dyes were also tested. Need for use of certified reference material (CRM) for SO₂ has also been emphasized.     

机场大气污染物高时间分辨率排放清单计算方法研究

通过研究机场大气污染物排放特征,结合我国相关排放政策及规范,以排放因子法为主要方法,设计了可建立机场高时间分辨率大气污染物排放清单的计算方法,以期为机场大气污染物排放实时监管提供研究基础。该方法针对飞机发动机和地面保障设备(GSE),实现了颗粒物、二氧化硫、氮氧化物等大气污染物和温室气体的半小时级别排放量计算。通过收集整理北京首都国际机场日航班计划与GSE运作情况实际数据,计算并建立了高时间分辨率的排放清单,验证了计算方法的可行性。随后,从活动水平误差和排放因子适用性两方面,对清单进行了不确定性分析,并通过计算结果对机场排放特征进行了分析,提出了减排建议。     

Evaluation of applicability of the Sartorius Airport MD8 sampler for detection of Bacillus endospores in indoor air

This study was designed to evaluate the measuring range and lowest limit of detection of Bacillus endospores in the ambient room air when the Sartorius MD8 sampler, and two different culture methods for bacterial enumeration were used. Different concentrations of bioaerosol were generated inside the test chamber filled with either the high-efficiency particulate air (HEPA)-filtered air or with the ambient room air. The detection of endospores in the HEPA-filtered air was achievable: (1) when they were aerosolized at a concentration above 7.56?×?10³ CFU/m³ and analyzed with spread plate method, and (2) when they were aerosolized at a concentration above 4.00?×?10² CFU/m³ and analyzed with pour plate method. The detection of endospores in the ambient room air was possible: (1) when they were aerosolized at a concentration above 9.1?×?10³ CFU/m³ and analyzed with spread plate method, and (2) when they were aerosolized at a concentration above 5.6?×?10² CFU/m³ and analyzed with pour plate method. The microorganisms present in the ambient room air interfere with precise quantification of Bacillus endospores when their concentration is relatively low. The results of this study may be helpful in critical assessment of the results obtained from monitoring the air for bacterial endospores.     

燃料燃烧排放系数的确定和估算方法

大气污染物的排放量主要与燃料种类及燃烧方式有关。鉴于目前仍未有一套针对不同燃料及不同燃烧方式而设计的燃料燃烧排放系数 ,现以广州市为研究对象 ,采用 5种不同的方法 ,得出一套适用于各种燃料及不同燃烧方式的排放系数 ,使得通过燃料消耗量推算大气污染物排放量更方便、更准确。     

对比分析法在环境空气质量预报业务中的应用

通过分析京津冀及周边区域环境空气质量预报的实际案例,从实时监测、污染源、大气条件以及数值预报模拟4个方面阐述了对比分析法在空气质量预报业务中的应用,帮助预报员比较类似污染源排放条件下的大气条件变化或者类似大气条件下的污染源变化,以便进一步开展量化分析。研究结果显示:利用时间同比、空间比较和大气条件对比的分析方法,能够判断在类似污染源排放和相似大气条件下,主要污染物的浓度水平、重污染发生、影响范围、持续时间、严重程度等污染特征以及污染物的水平传输影响等;采用污染源变化对比分析法,能够获得在类似大气条件下,污染源排放的减少或剧增对主要污染物浓度水平的影响程度;通过数值预报模式结果对比分析,能够获得在类似的污染源排放条件下,大气环流形势的稳定程度和变化情况,从而判断其对污染物浓度水平的影响。对比分析法是开展京津冀及周边区域环境空气质量预报业务中的重要环节,有利于持续提高空气质量预报的准确率,供全国空气质量预报员开展辖区空气质量预报时参考。     

Determination of technical grade isocyanates used in the production of polyurethane plastics

A method for determination of technical grade isocyanates used in the production of polyurethane (PUR) is presented. The isocyanates in technical grade products were characterised as di-n-butylamine (DBA) derivatives using LC-MS and LC-chemiluminescent nitrogen detection (CLND) and the total isocyanate content was compared to a titration assay. For collection of isocyanates in air, an impinger-filter sampling technique with DBA as derivatisation reagent was used. Characterised DBA and nonadeuterium labelled DBA derivatives of isocyanates in technical products were used as calibration standards and internal standards, respectively, in the analysis of air samples. Three workplaces were studied where PUR products were produced either by spraying or by moulding. In both technical products and in air samples, a number of monomeric, oligomeric and prepolymeric isocyanates of e.g. methylenebisphenyl diisocyanate (MDI) and hexamethylene diisocyanate (HDI) were characterised. Several of these have not previously been described in workplace atmospheres. In the technical isocyanate products, between 69 and 102% of the NCO content determined by titration was accounted for by LC-CLND. Quantifications of a wide range of isocyanates in air samples were performed with correlation coefficients in the range 0.988-0.999 (n= 8) and the instrumental detection limits were 0.7-25 pg. At the two workplaces where MDI- and HDI isocyanurate-based products were sprayed, the isocyanate composition in the air reflected the composition in the technical product. At the workplace where a MDI-based product was used in a moulding process, only the monomeric isocyanates were found in the air. The advantage of using characterised technical grade isocyanates as analytical standards was clearly demonstrated and the possibility of using index compounds when monitoring isocyanate exposure is discussed.     

大气乙醛碳同位素分析方法的研究

利用气相色谱/燃烧/同位素比值质谱(GC/C/IRMS)分析技术,采用NaHSO3与半胱胺衍生化方法,测定了气态乙醛在衍生化反应过程中的碳同位素效应,探讨了采用该方法测定大气乙醛碳同位素组成的可行性。试验测定了乙醛、衍生剂半胱胺及相应衍生物的碳同位素比值,结果表明,乙醛衍生物的δ13C测量值与理论值的偏差范围为0.11‰～0.35‰,在仪器精密度范围内(<0.50‰),即在衍生化过程中基本不会发生碳同位素分馏。采用该方法初步测定了大气中乙醛的碳同位素组成,实测数据显示,广州地化所和肇庆鼎湖山大气乙醛δ13C平均值分别为(-34.21±0.27)‰和(-31.23±0.16)‰,相同采样点的大气乙醛碳同位素组成基本不变,可见该方法可作为研究大气乙醛不同排放源的一种有效方法。     

隧道路面沥青摊铺过程空气中TSP和多环芳烃污染研究

分析了隧道沥青摊铺过程环境空气中的TSP及多环芳烃质量浓度。TSP用膜法,中流量采样器采样15 min,重量法分析;超声波萃取,高效液相色法分析多环芳烃。结果表明,摊铺机周围空气中TSP超过8 mg/m3,道路空气中TSP超过3 mg/m3;环境空气中苊烯等12种多环芳烃均有检出,苊烯和艹屈质量浓度较高,苯并[a]芘和二苯并[a,h]蒽质量浓度较低。苯并[a]蒽、苯并[a]芘和二苯并[a,h]蒽超标,对人体健康危害较大。建议加强相关行业PAHs的排放水平及其健康风险研究,制定相关限值标准和沥青摊铺过程环境空气的沥青烟监测方法标准。