气相色谱法测定环境空气中1,2-环氧丙烷

以活性炭吸附环境空气中 1,2 -环氧丙烷 ,用二硫化碳洗脱 ,OV - 10 1:30m× 0 32mm× 0 2 5 μm毛细管柱低温分流进样分离 ,氢火焰离子化检测器测定 ,保留时间定性 ,峰高定量 ,采样吸附率达 99%。方法有较宽的线性范围 ,较高的灵敏度和精密度。当采样体积为 30L时 ,1,2 -环氧丙烷的检测限为 0 0 0 5mg/m3     

全二维气相色谱/飞行时间质谱联用监测环境空气中VOCs

采用全采样系统-全二维气相色谱/飞行时间质谱联用技术监测环境空气中的VOCs,优化了调制周期、升温程序、进样体积等分析条件.39种目标化合物在0 μg/m3～10.0 μg/m3范围内线性良好,检出限范围为0.03 μg/m3～0.09 μg/m3,标准气体平行测定的RSD为1.1％ ～5.3％.应用于化工园区环境空气样品测定,与热脱附-气相色谱/质谱法相比,目标物的分离效果更佳.     

GDX 502管吸附-二氯甲烷解吸-气相色谱法测定气中的吡啶

建立了GDX 502管吸附-二氯甲烷解吸-气相色谱测定气中吡啶的方法,考察吸附管类型、解吸溶剂、解吸溶剂体积、采样时间和采样流量对测定结果的影响。结果表明,气中吡啶用GDX 502吸附管以0. 5 L/min的流量采样20 min,二氯甲烷解吸至1 m L,DB-1 (30 m×250μm×0. 25μm)柱分离,空白样品低、中、高3种加标量回收率为90. 8%～108%(n=6),相对标准偏差为2. 9%～4. 4%,方法在0～19. 6 mg/L线性范围内响应良好,相关系数(r)=0. 999 9。当采样体积为10 L时,检出限为0. 01 mg/m~3。该方法重复性好、回收率高、干扰较小,能够满足空气和废气中吡啶分析的要求。     

DNPH衍生化采样-溶剂解析-高效液相色谱法同时测定木制品中25种醛酮化合物

建立了DNPH衍生化采样-溶剂解析-高效液相色谱测定木制品中醛酮化合物的方法。采样时需在2,4-二硝基苯肼吸附管前串联一只SEP-PAK脱臭氧小柱;采样体积应≤10 L,流量≤400 m L/min。该法对25种醛(酮)化合物对应的衍生物分离效果良好,在0.005~3 mg/L范围内线性良好,相关系数R2≥0.999 6,回收率为85.3%~113.5%,精密度为2.67%~4.56%。采样量为10 L时,25种醛(酮)化合物的检出限和定量限分别≤0.16和0.50μg/m3。     

毛细管柱气相色谱法测定环境空气中1,2-二氯乙烷

采用毛细管柱气相色谱法测定环境空气中的1,2-二氯乙烷,用活性碳吸附,二硫化碳解析,FID检测器分析.方法在0 mg/L～311mg/L范围内线性良好,当采样体积为20 L时,最低检出质量浓度为0.006 mg/m3,标准溶液平行测定的RSD≤2.2%,加标回收率为98.4%～101%.     

环境空气中丙烯酸乙酯的气相色谱法测定

建立了环境空气中丙烯酸乙酯的TenaxGC吸附 -热解吸气相色谱测定方法。方法回收率为 87 3%～1 0 7 1 % ,变异系数为 5 3%～ 7 2 %。当采样体积为 2L时 ,检测限为 0 0 2mg/m3,具有采样时间短 ,不用任何溶剂等特点。     

离子色谱法同时测定大气中二氧化硫和氮氧化物

建立以2.2mmol/L的Na2CO3和2.7mmol/L的NaHCO3的混合溶液为吸收液,同时串联两个大气采样瓶采样,第一个采样瓶的吸收液内含质量体积比为0.05%的乙二胺四乙酸二钠盐(EDTA)吸收大气中SO2和NO2,第二个采样瓶的吸收液中内舍质量体积比为0.9%的过氧化氢采集大气中的NO,采样后用离子色谱法测定,若用10ml吸收液,采样体积为30L时,SO2的检出限为0.004mg/m3,可测浓度范围为0.03～26.7mg/m3;NO2的检出限为6.7×10-4mg/m3,可测浓度范围为0.03～20mg/m3.方法简便快速、准确、选择性好,完全满足环境监测对大气中二氧化硫和氮氧化物的同时测定.     

毛细管柱气相色谱法测定环境空气中的樟脑

采用毛细管柱气相色谱氢火焰离子化检测器测定环境空气中的樟脑,选择硅胶为吸附剂,甲醇/丙酮混合溶剂(体积比90∶10)为解析剂.方法在0.544 mg/L～109 mg/L范围内线性良好,检出限为0.06 mg/L,当采样体积为20 L时,最低检出质量浓度为0.003 mg/m3,标准溶液平行测定的RSD≤3.8％,空白...     

加速溶剂萃取-高效液相色谱法测定环境空气中的苯并(a)芘

采用加速溶剂萃取一高效液相色谱法荧光检测器测定环境空气中的苯并（a）芘，以乙腈／水为流动相，检测器激发波长为290nm，发射波长为430nm。方法线性良好，检出限为0．08μg／L，当采样体积为1080m。时，最低检测质量浓度为3×10^-7μg／m^3（标准状态下），实际样品加标回收率为87．2％～109％。与超声波萃取法相比，两种方法回收率相近，而加速溶剂萃取法乙腈用量更少。     

微波消解ICP-AES法测定废气中铅镉砷

采用微波消解电感耦合等离子体发射光谱法同时测定废气中的铅、镉、砷,在优化的试验条件下,方法在0 mg/L～5.00 mg/L范围内线性良好,铅、镉、砷的检出限分别为0.250 μg/m3、0.125 μg/m3、0.375 μg/m3(按采样体积400 L、定容体积50 mL计),空白滤筒平行测定6次的RSD为2.3％～10.5％,加标回收率为83％ ～ 112％,与标准方法的测定结果无显著差异.     

A New Mathematical Approach in Environmental and Life Sciences: Gene–Environment Networks and Their Dynamics

An important research area in life sciences is devoted to modeling, prediction, and dynamics of gene-expression patterns. As clearly understood in these days, this enterprise cannot become satisfactory without acknowledging the role of the environment. To a representation of past, present, and most likely future states, we also encounter measurement errors and uncertainties. This paper surveys and improves recent advances in understanding the foundations and interdisciplinary implications of the newly introduced gene–environment networks, and it integrates the important theme of carbon dioxide emission reduction into the networks and dynamics. We also introduce some operational and managerial issues of practical working and decision making, expressed in terms of sliding windows, quadrants (modules) of parametric effects, and navigating (controlling) between such effects and directing them. Given data from DNA microarray experiments and environmental records, we extract nonlinear ordinary differential equations that contain parameters that have to be determined. For this, we employ modern (Chebychevian) approximation and (generalized semi-infinite) optimization. After this is provided, time- discretized dynamical systems are studied. A combinatorial algorithm with polyhedra sequences allows to detect the region of parametric stability. Finally, we analyze the topological landscape of gene–environment networks with its structural (in)stability. By embedding as a module and investigating CO₂ emission control and figuring out game theoretical aspects, we conclude. This pioneering work is theoretically elaborated, practically devoted to health care, medicine, education, living conditions, and environmental protection, and it invites the readers to future research.      

Assessing health consequences in an environmental impact assessment: The case of Amsterdam Airport Schiphol

In this article a comprehensive approach for the evaluation of possible health effects in an environmental impact assessment (EIA) is described, illustrated with the example of Amsterdam Airport Schiphol. Unlike many EIAs, we estimated quantitatively the impact of aircraft-related pollution in terms of the number of affected people for aircraft noise annoyance, odour annoyance and hypertension. In addition, an analysis of health registry data on cardiovascular and respiratory diseases and a short survey on annoyance and risk perception were carried out. The scope of a health impact assessment depends on the situation, available knowledge and data, concern in the population about the impact and the number of people concerned. It is important to pay attention to the perception of risks and concerns from all parties involved. Moreover, the results demonstrate that far more people outside the area for which standards apply were affected than inside.     

Contaminant Profiles of Two Species of Shorebirds Foraging Together at Two Neighboring Sites in South San Francisco Bay, California

The San Francisco Bay estuary isused by over one million shorebirds during springmigration and is home to several hundred thousandduring the winter. Most shorebird use occurs in thesouthern reach of the estuary (South Bay). Thereduced water circulation and discharge fromindustrial sources in the South Bay are responsiblefor the highest levels of some trace elements in theestuary. Wintering shorebirds have been found to havestrong site fidelity to areas as small as a fewkilometers in the South Bay, which may increase theirexposure to contaminants near local point sources. Inaddition, different shorebird species foraging at thesame site have been shown to have differentcontaminant burdens. Thus, our objectives were totest whether contaminant burdens differed by species,or whether contaminant burdens differed in shorebirdscollected at adjacent sites. We examined thecontaminant profiles of two species of shorebirds,long-billed dowitchers (Limnodromus scolopaceus)and western sandpipers (Calidris mauri) thatforage together at two sites, Hayward and Newark,separated by 8 km in the South Bay. We usedmultivariate analysis of variance tests to compare thecomposition of 14 elemental analytes in their livertissues and estimated their molar ratios of Hg and Se. Composite samples were used for contaminant analysesbecause of the small body size of the shorebirds. Seven elemental analytes (Ag, Ba, Be, Cr, Ni, Pb, V)were below detection limits in a majority of thesamples so statistical analyses were precluded. Inthe measurable analytes (As, Cd, Cu, Hg, Mn, Se, Zn),we found no significant intra-site differences ofcontaminant profiles for the two species. We pooledthe samples to examine inter-site differences andfound significant differences in contaminant profilesbetween shorebirds at the neighboring sites (P = 0.03). Shorebirds at Newark had higher (P < 0.05) concentrations of As, Cd, and Se than those at Hayward. Dowitchers at Newark had concentrations of Hg and Se which were highly correlated (P < 0.003) in a mean molar ratio of 1:19, similar tothat reported in other birds. In the larger dowitcherspecies, we also examined exposure to 20organochlorine compounds. Organic analyses showedthat the dowitchers had been exposed to DDE, PCBs,dieldrin and trans-nonachlor, but with no significantdifferences in concentrations between Hayward andNewark (P > 0.05).     

土壤和底泥中砷、铬、锰测定的前处理技术

试验了土壤和底泥中砷的前处理技术，其目的是能对土壤、底泥中砷、铬、锰在一次前处理中制备成试液，比色法分析。试验表明，用Ｈ２ＳＯ４－Ｈ３ＰＯ４－Ｈ２Ｏ２进行前处理是可行的。方法简单、挥发酸雾少，用标准参考物质检验证明，分解完全，数据准确，有粒较好一致性。     

Geochemical assessment of metal transport in glacial till during electrokinetic remediation

This paper presents the chemical speciation and retention behavior of chromium (Cr), nickel (Ni), and cadmium (Cd) prior to and after the electrokinetic remediation in glacial till soil. The speciation of the metals was predicted using the chemical speciation program MINEQL⁺. The simulations were performed for single-contaminant with only Cr(VI) or Ni, and multi-contaminants consisting of: (1) Cr(VI), Ni, and Cd; (2) Cr(III), Ni and Cd; (3) Cr(VI), Cr(III), Ni and Cd; (4) Cr(VI), Ni, and Cd with reducing agents; and (5) Cr(III), Ni, and Cd with oxidizing agent (Mn). The results showed that the speciation and distribution of cationic metals [Ni, Cd, and Cr(III)] in glacial till soil remain unaffected or slightly affected during electrokinetics. This is attributed to the high pH buffering capacity of the glacial till, leading the metals to precipitate in the soil prior to and after electrokinetics. This study showed that during electrokinetics, Cr(VI) existed as anionic complex and migrated towards the anode and the migration is maximum in case of a single-contaminant system. The study also showed that near the anode in the absence of any reducing and oxidizing agent, Cr(VI) mostly adsorbed, and some of Cr(VI) reduced to Cr(III) and migrated towards the cathode and finally precipitated due to high pH conditions. Ni and Cd remain adsorbed or precipitated due to the high pH conditions throughout the soil. Among the reducing agents, the sulfide had significant effect on the migration of metals compared to ferrous ions. While in the presence of oxidizing agent (Mn), no noticeable Cr(VI) was found in the soil sample indicating the reduction of Cr(VI) to Cr(III) and the predominance of reducing conditions due to the presence of naturally occurring iron in the glacial till soil. Overall, this study provides a reasonable explanation of the speciation and distribution of chromium, nickel and cadmium during the electrokinetic remediation of glacial till soil.     

Biomonitoring of Lead, Zinc, and Cadmium in Streams Draining Lead-Mining and Non-Mining Areas, Southeast Missouri, USA

We evaluated exposure of aquatic biota to lead (Pb), zinc (Zn), and cadmium (Cd) in streams draining a Pb-mining district in southeast Missouri. Samples of plant biomass (detritus, periphyton, and filamentous algae), invertebrates (snails, crayfish, and riffle benthos), and two taxa of fish were collected from seven sites closest to mining areas (mining sites), four sites further downstream from mining (downstream sites), and eight reference sites in fall 2001. Samples of plant biomass from mining sites had highest metal concentrations, with means 10- to 60-times greater than those for reference sites. Mean metal concentrations in over 90% of samples of plant biomass from mining sites were significantly greater than those from reference sites. Mean concentrations of Pb, Zn, and Cd in most invertebrate samples from mining sites, and mean Pb concentrations in most fish samples from mining sites, were also significantly greater than those from reference sites. Concentrations of all three metals were lower in samples from downstream sites, but several samples of plant biomass from downstream sites had metal concentrations significantly greater than those from reference sites. Analysis of supplemental samples collected in the fall of 2002, a year of above-average stream discharge, had lower Pb concentrations and higher Cd concentrations than samples collected in 2001, near the end of a multi-year drought. Concentrations of Pb measured in fish and invertebrates collected from mining sites during 2001 and 2002 were similar to those measured at nearby sites in the 1970s, during the early years of mining in the Viburnum Trend. Results of this study demonstrate that long-term Pb mining activity in southeast Missouri has resulted in significantly elevated concentrations of Pb, Cd, and Zn in biota of receiving streams, compared to biota of similar streams without direct influence of mining. Our results also demonstrate that metal exposure in the study area differed significantly among sample types, habitats, and years, and that these factors should be carefully considered in the design of biomonitoring studies.     

Comparative studies on accumulation of Cr from metal solution and tannery effluent under repeated metal exposure by aquatic plants: its toxic effects

The present study demonstrates comparison of Cr accumulatingpotential by the plants of Najas indica Cham. (submerged),Vallisneria spiralis L. (rooted submerged) and Alternanthera sessilis R. Br. (rooted emergent) under repeatedmetal exposure and its effect on chlorophyll and protein concentrations. These plants were treated with different concentrations of Cr under repeated exposure in controlled laboratory conditions to assess the maximum metal accumulationpotential. The plants of V. spiralis accumulated significantly high amount of Cr under laboratory conditions incomparison to N. indica and A. sessilis. The maximumaccumulation of 1378, 458 and 201 g g^-1 dw Cr was found in the leaves of V. spiralis, N. indica and A. sessilis, respectively at 8 mg L^-1 after 9 day of Cr exposure. These plants have shown a decrease in chlorophyll andprotein concentrations with increase in Cr concentrations. In view of high accumulation of Cr in V. spiralis, the plantswere treated with different concentrations of tannery effluent collected from Common Effluent Treatment Plant, Unnao (UP). Theplants of V. spiralis treated with 100% tannery wastewatershowed the maximum accumulation (57.5 g g^-1 dw) of Cr in the roots after 10 days of exposure. The plants were foundeffective in removing Cr from solution and tannery effluent.     

一起河流砷污染事故的处置与监测分析

介绍了大沙河砷污染事故的处置和监测分析。多介质排查监测摸清了污染的范围和程度,为治理工作提供了科学依据,污染治理措施有效控制了污染的扩散;监测数据表明,治理措施将水中砷污染物沉降至河床使污染水质达标排放。吸附了大量砷化合物的底泥被清理并进一步处置,多介质跟踪监测应持续进行直至不存在潜在危害。     

核应急辐射环境监测的准备和响应

日本核泄漏事故引发的核危机为人类安全和平地利用核能又一次敲响了警钟.核事故应急工作作为减小核电站危害环境和公众安全的最后屏障,将起到重要的作用,必须做好相关的准备和响应工作.核应急辐射环境监测工作是核应急工作的重要组成部分,在对核应急辐射环境监测进行准备和响应时主要遵循实用性、适用性和适度性并兼顾常规和应急监测的“平战...