环境监测用正己烷气体标准样品的研制

采用称量法通过两步稀释制备了含量水平为1μmol/mol的氮气中正己烷气体标准样品,考察了气瓶内壁吸附作用、制备重现性、瓶内均匀性、时间稳定性等相关因素的影响,并将该正己烷气体标准样品与同类气体标准样品进行了比较。结果表明:该正己烷气体标准样品的最低使用压力为1 MPa,有效期为12个月(0~38℃),相对扩展不确定度(k=2)为2%;该正己烷气体标准样品的量值与同类标准样品具有可比性,可为相关环境监测工作提供技术支持。     

水污染分析校准用汞溶液的研制

研制了水污染分析校准用汞溶液。采用原子荧光光谱法对样品进行了均匀性和稳定性检验,对样品的量值进行了验证并进行了不确定度评定。检验结果表明:汞溶液均匀性良好,室温条件下可稳定36个月以上;样品的标准值为100 mg/L,扩展不确定度为2 mg/L。样品量值与美国AccuStandard公司同种标准物质具有一致性。可用于水中汞检测的测定标准、质量控制、分析方法研究以及实验室能力验证等方面。     

全自动消解-电感耦合等离子体质谱法测定土壤中16种元素

采用HNO_3-HF-HClO_4消解体系,建立了全自动消解-电感耦合等离子体质谱仪测定土壤中~(75)As、~9Be、~(51)V、~(55)Mn、~(59)Co、~(60)Ni、~(63)Cu、~(66)Zn、~(98)Mo、~(111)Cd、~(138)Ba、~(205)Tl、~(208)Pb、~(107)Ag、~(52)Cr、~(121)Sb等16种元素的新方法。通过碰撞池技术和编辑干扰元素校正方程有效校正了质谱干扰,并用内标校正了土壤基体干扰。用土壤标准物质GSS-13验证该方法,其校准曲线相关系数大于0.999 9,方法检出限在0.005~0.5μg/g之间,RSD为0.22%~2.35%,加标回收率为92%~114%。采用该方法测定实际土壤样品,加标回收率为93%~123%。     

加压流体萃取—气相色谱-质谱法检测土壤中邻/间/对硝基甲苯

建立加压流体萃取—气相色谱-质谱法检测土壤中邻/间/对硝基甲苯的含量.选用二氯甲烷-正己烷混合溶液(体积比1:1)作为萃取溶剂,采用加压流体萃取仪对冷冻干燥土壤样品进行萃取,经硅酸镁小柱净化后,内标法定量.实验结果表明,邻/间/对硝基甲苯在质量浓度1.0～20.0μg/mL范围内线性关系良好,相关系数不小于0.999,...     

基质固相分散萃取—气相色谱法测定土壤中有机氯农药含量

建立了一种基质固相分散萃取—气相色谱法测定土壤中8种有机氯农药含量的方法,优选了固相分散剂及其用量、洗脱溶剂以及土壤样品与分散剂的质量比。实验结果表明,在弗罗里硅土作为分散剂、正己烷和丙酮（体积比为1∶1）为洗脱溶剂、土壤样品与分散剂的质量比为1∶3的优化条件下,8种有机氯农药在50~250 μg/kg范围内表现出良好的线性关系,相关系数大于0.99,加标回收率为60.3%~94.3%,相对标准偏差为6.83%~8.95%。实际土壤质控样测试结果显示,本方法的测试结果在标准值的不确定度范围内,可满足土壤中有机氯农药残留的检测分析。     

液液萃取—GC-MS法同时测定石化废水中双酚A和邻苯二甲酸二乙酯

建立了液液萃取(LLE)—气相色谱-质谱(GC-MS)法同时测定石化废水中双酚A(BPA)和邻苯二甲酸二乙酯(DEP)的新方法,对液液萃取条件进行了优化。最佳的液液萃取条件为:萃取剂为乙酸乙酯,水样调成酸性(pH2),每次加入萃取剂0.1 mL/mL、盐析剂NaCl 0.1 g/mL,萃取次数为6次,每次萃取时间为2 min。实验结果表明:在质量浓度1～100 mg/L的范围内,BPA和DEP测定标准曲线的线性关系良好;BPA和DEP的检出限(LOD)分别为5.18μg/L和0.89μg/L,定量限(LOQ)分别为17.11μg/L和2.96μg/L,回收率为81.4%～124.9%,相对标准偏差(RSD)(n=7)小于5.5%。     

浊点萃取分光光度法测定水中Cr(Ⅵ)

利用二苯碳酰二肼显色,Triton X-100-正辛醇浊点萃取,建立了一种分光光度法测定水中Cr(Ⅵ)的新方法,并探讨了不同测定条件对测定效果的影响。优化后的测定条件为(总体积50 mL)1 mol/L稀硫酸加入量1.0mL、2 g/L二苯碳酰二肼溶液加入量1.5 mL、10 g/L Triton X-100溶液加入量1.5 mL、3 g/L苯甲酸溶液加入量4.0mL、正辛醇加入量5.0 mL。Cr(Ⅵ)质量浓度在0~20μg/L范围内符合朗伯-比尔定律,线性回归方程的相关系数为0.995 5。该方法应用于水样中痕量Cr(Ⅵ)的测定,相对标准偏差小于2.5%,加标回收率为95.7%。     

西瓜、瓜叶及瓜田土壤中乙撑硫脲残留量的液相色谱分析方法研究

建立了一种采用高效液相色谱仪测定乙撑硫脲（ETU）在西瓜、瓜叶和瓜田土壤中残留量的分析方法。空白样品标准添加浓度为0.05-10.0mg/kg时,平均回收率为83.2%-90.7%,变异系数＜12.5%,样品中ETU的最低检出浓度为0.02mg/kg。该方法的准确度和灵敏度较高。应用本方法测定西瓜、瓜叶和瓜田土壤的 ETU残留量,取得了满意的结果。     

生物过滤法去除空气中的甲醛

采用生物过滤法处理甲醛废气,研究了填料类型、填料厚度及植物(吊兰)根系对甲醛去除效果的影响。实验结果表明:采用有机土壤、陶粒和蛭石末的混合材料为生物过滤塔的填料时,甲醛去除率高于以普通土壤为填料;当甲醛进口质量浓度为0~0.300g/m3、混合材料厚度为100mm时,处理后出口甲醛质量浓度为0~0.003g/m3,低于GB/T16297—1996《大气污染物综合排放标准》排放标准(0.03g/m3);当混合材料厚度为100mm时,距离吊兰根系(水平距离)100mm处的甲醛质量浓度最小,表明吊兰根系对生物过滤塔的甲醛去除效果有影响。     

第一部分 粉煤灰标样制备

本文分三部分介绍粉煤灰标准样品的研制过程。第一部分为标样的制备,第二部分为标样的理化性质和均匀性检查,第三部分为标样的定值,数据处理及稳定性试验。     

中国有机氯农药的监测现状

归纳了有机氯农药在我国的生产和使用概况，总结了我国大气、水体和沉积物、土壤以及生物体等环境介质中的有机氯农药监测现状。在此基础上，对我国有机氯农药的深入研究提出了建议。     

黑麦草-不动杆菌组合体系对石油污染土壤的生物强化修复

以盆栽实验为基础，研究了植物（黑麦草，Lolium perenne L）-微生物（不动杆菌，Acinetobacter sp.）组合体系对石油污染土壤的修复效果。实验结果表明：在总石油烃含量为4 420.18 mg/kg、脱氢酶活性为230.52 μg/（g·d）、苯酚毒性当量浓度（TEQphenol）为1 633.21 mg/L的初始条件下，强化组总石油烃降解率最高为53.08%，是对照组的1.60倍；土壤的脱氢酶活性达到637.73 μg/（g·d），是对照组的10.64倍；石油污染土壤的生物毒性大幅降低， TEQphenol最终降低至171.08 mg/L。说明该组合体系对石油污染土壤具有很好的修复作用，且微生物对土壤中有毒物质的降解起主要作用。     

Remediation of Persistent Organic Pollutants Using a Novel Two-Phase Soil Washing Biosorption Process

A two-phase soil washing biosorption process was developed for the remediation of p,p-DDT-contaminated soil. The process involved desorption of contaminants from soil using dilute primary alcohols (40% 1-propanol) followed by contaminant removal from cosolvent solutions using fungal biosorption. Bench scale remediation studies were preformed to simulate ex situ (recycling experiment) or in situ (soil column study) treatment strategies. Both systems were effective at cleaning the soil to below Australian regulatory p,p-DDT levels. After 50–80 hours of soil washing, over 93% of p,p-DDT was removed from the soil(990 mg kg^-1 to <65 mg kg^-1) using either of these methods.p,p-DDT was removed from the cosolvent phase by sorption onto the fungal biomass. This resulted in only low levels of p,p-DDT remaining in the cosolvent solution(<1.5 mg l^-1). The application of both treatment strategies resulted in the rapid clean up of p,p-DDT-contaminated soil and the potential to recycle cosolvent solutions. The ability to recycle cosolvent solutions provides a mechanism for cost reductions of the remediation strategy.     

Phytoremediation: The uptake of metals and metalloids by rhodes grass grown on metal‐contaminated soil

An experiment was performed to examine the phytoremediation potential of Rhodes grass (Chloris gayana Kunth cv. ‘Pioneer’). The study sought to determine substrate tolerance, biomass production, and plant uptake of antimony (Sb), arsenic (As), cadmium (Cd), lead (Pb), silver (Ag), and zinc (Zn). The plants were grown on weight percent mixtures (5 percent, 15 percent, 25 percent, 35 percent, 50 percent) of a vertisol soil and base‐metal mine tailings (7–2,040 μg/g As, ≥ 30 μg/g Cd, 30–12,000 μg/g Pb, and 72–4,120 μg/g Zn). The 5 percent and 15 percent amendment of mine tailings increased the biomass production of Rhodes grass (from 0.1 g/plant to ≈ 3.5 g/plant) without appreciably elevating plant concentrations of the elements. Plant growth decreased by greater than 50 percent for the substrate containing greater than 25 percent tailings (3,023 μg/g Pb and 1,084 μg/g Zn). Reduced biomass production coincided with maximal Zn uptake by Rhodes grass (249.8 μg/g), indicating tailings induced phytotoxicity. The total concentrations of metals and metalloids tolerated by Rhodes grass in the plant‐growth medium indicated hypertolerance to elevated As, Pb, and Zn concentrations. Partial extraction of the plant‐growth medium determined that plant‐available Pb was ten times higher than Ag, As, Cd, and Zn availability. However, Rhodes grass accumulated low levels of Pb, in addition to As and Cd, over the experimental range, indicating low fodder toxicity risk to browsing livestock. This study concludes that if there are no invasive species issues associated with conservation land uses, Rhodes grass is well suited to metalliferous mined land revegetation and would therefore be highly effective for such programs in subtropical and tropical Australia. © 2005 Wiley Periodicals, Inc.     

陕北某采油厂石油污染土壤的修复示范工程

调查了陕北某采油厂油井周边石油污染土壤的基本污染情况,采用铜绿假单胞菌-黑麦草联合修复技术对其进行了现场修复示范工程,取得了较好的现场修复效果。调查显示,该油井周边土壤的含油量最高为9 020 mg/kg。90 d的修复周期结束后,土壤的含油量降至402 mg/kg,去油率高达95.5%,并且不同采样位置的土壤含油量检测结果均低于500 mg/kg,满足《农用污泥污染物控制标准》（GB 4284—2018）中的A级土壤标准。单独使用黑麦草或铜绿假单胞菌进行修复,土壤的去油率分别为29.5%或88.8%,而空白区土壤的去油率仅为21.8%。     

Emissions of organo-metal compounds via the leachate and gas pathway from two differently pre-treated municipal waste materials -- A landfill reactor study

Due to their broad industrial production and use as PVC-stabilisers, agro-chemicals and anti-fouling agents, organo-metal compounds are widely distributed throughout the terrestrial and marine biogeosphere. Here, we focused on the emission dynamics of various organo-metal compounds (e.g., di,- tri-, tetra-methyl tin, di-methyl mercury, tetra-methyl lead) from two different kinds of pre-treated mass waste, namely mechanically-biologically pre-treated municipal solid waste (MBP MSW) and municipal waste incineration ash (MWIA). In landfill simulation reactors, the emission of the organo-metal compounds via the leachate and gas pathway was observed over a period of 5 months simulating different environmental conditions (anaerobic with underlying soil layer/aerated/anaerobic). Both waste materials differ significantly in their initial amounts of organo-metal compounds and their environmental behaviour with regard to the accumulation and depletion rates within the solid material during incubation. For tri-methyl tin, the highest release rates in leachates were found in the incineration ash treatments, where anaerobic conditions in combination with underlying soil material significantly promoted its formation. Concerning the gas pathway, anaerobic conditions considerably favour the emission of organo-metal compounds (tetra-methyl tin, di-methyl mercury, tetra-methyl lead) in both the MBP material and especially in the incineration ash.     

Challenges of soil mixing using catalyzed hydrogen peroxide with rotating dual axis blending technology

Although known to be one of the most effective oxidants for treatment of organic contaminants, catalyzed hydrogen peroxide (CHP) is typically not used for soil mixing applications because of health and safety concerns related to vapor generation and very rapid rates of reaction in open excavations. In likely the first large‐scale in situ CHP soil mixing application, an enhanced CHP, modified Fenton's reagent (MFR), was applied during soil mixing at the Kearsarge Metallurgical Superfund Site in New Hampshire. An innovative rotating dual‐axis blender (DAB) technology was used to safely mix the MFR into low‐plasticity silt and clay soils to remediate residual 1,1,1‐trichloroethane (111TCA); 1,1‐dichloroethene (11DCE); and 1,4‐dioxane (14D). It was expected that the aggressive treatment approach using relatively “greener” hydrogen peroxide (HP) chemistry would effectively treat Site contaminants without significant byproduct impacts to groundwater or the adjacent pond. The remediation program was designed to treat approximately 3,000 cubic yards of residual source area soil in situ by aggressively mixing MFR into the soils. The subsurface interval treated was from 7 to 15 feet below ground surface. To accurately track the soil mixing process and MFR addition, the Site was divided into 109 10‐foot square treatment cells that were precisely located, dosed, and mixed using the DAB equipped with an on‐board GPS system. The use of stabilizing agents along with careful calculation of the peroxide dose helped to ensure vapor‐free conditions in the vicinity of the soil mixing operation. Real‐time sampling and monitoring were critical in identifying any posttreatment exceedences of the cleanup goals. This allowed retreatment and supplemental testing to occur without impacting the soil mixing/in situ chemical oxidation (ISCO) schedule. Posttreatment 24‐hr soil samples were collected from 56 random locations after ensuring that the HP had been completely consumed. The posttreatment test results showed that 111TCA and 11DCE concentrations were reduced to nondetect (ND) or below the cleanup goals of 150 μg/kg for 111TCA and 60 μg/kg for 11DCE. Supplemental posttreatment soil samples, collected six months after treatment, showed 100 percent compliance with the soil treatment goals. Groundwater samples collected one year after the MFR soil mixing treatment program showed either ND or low concentrations for 111TCA, 11DCE, and 14D. Successful stabilization and site restoration was performed after overcoming considerable challenges associated with loss of soil structure, high liquid content, and reduced bearing capacity of the blended soils.     

Evaluation of bangkok sewage sludge for possible agricultural use.

Bangkok (Thailand) covers more than 1500 km2 and has 10 million inhabitants. The disposal of wastewater is creating huge problems of pollution. The estimated amount of sewage sludge was estimated to be around 108 tonnes dry matter (DM) per day in 2005. In order to find a lasting way of disposal for this sewage sludge, the suitability of the sludge produced from three waste-water treatment plants for use as fertilizing material was investigated. Monthly samplings and analysis of sewage sludge from each plant showed that the composition of sludge varied according to the area of collection and period of sampling, and there was no link to rainfall cycle. Plant nutrient content was high (i.e. total N from 19 to 38 g kg(-1) DM) whereas organic matter content was low. The concentrations of heavy metals varied between sludge samples, and were sometimes higher than the E.U. or U.S. regulations for sewage sludge use in agriculture. Faecal coliforms were present in the sludge from one of the plants, indicating a possible contamination by night soil. In order to decrease this potentially pathogenic population the sewage sludge should be heated by composting. As the C/N ratio of sewage sludge was low (around 6) some organic by-products with high carbon content could be added as structural material to enhance the composting.     

Optimum moisture levels for biodegradation of mortality composting envelope materials

Moisture affects the physical and biological properties of compost and other solid-state fermentation matrices. Aerobic microbial systems experience different respiration rates (oxygen uptake and CO2 evolution) as a function of moisture content and material type. In this study the microbial respiration rates of 12 mortality composting envelope materials were measured by a pressure sensor method at six different moisture levels. A wide range of respiration (1.6-94.2mg O2/g VS-day) rates were observed for different materials, with alfalfa hay, silage, oat straw, and turkey litter having the highest values. These four envelope materials may be particularly suitable for improving internal temperature and pathogen destruction rates for disease-related mortality composting. Optimum moisture content was determined based on measurements across a range that spans the maximum respiration rate. The optimum moisture content of each material was observed near water holding capacity, which ranged from near 60% to over 80% on a wet basis for all materials except a highly stabilized soil compost blend (optimum around 25% w.b.). The implications of the results for moisture management and process control strategies during mortality composting are discussed.     

Microbial Activity in Relation to Small Scale Patterns of Heavy Metals and Substrate Quality in Spruce Mor Layers (Of) in Southern Sweden

The within-site correlations between soil respiration rates,lead (Pb), mercury (Hg) and cadmium (Cd) concentrations andorganic matter quality variables were investigated at four sites in southern Sweden. The aim was to study whether the within-site variation in heavy metal concentrations could beused to monitor biological effects of regional deposition of heavy metals. Two sites in the south-west, one in the mid-southof the country, and one in south-east were investigated. At the south-eastern, least contaminated, site there were no correlations between soil respiration rate, and either organicmatter quality variables or heavy metal concentrations. At the remaining sites, negative correlations were found between Pb andsoil respiration rate. However, at two of these three sites there was a covariation with cellulose that could account for these correlations. The within-site variation of pH and total nitrogen (N) was low, and did not show any correlative general trends with either respiration rate or heavy metals. Meta analysis showed that negative correlations between Pb or Hg, on the one hand, and cellulose or hemicellulose on the other weregenerally found in within-site investigations. However, this does not necessarily explain the correlation between Pb and soil respiration, as was shown for the southernmost site. A PLS model of soil respiration rates at this site, using allmeasured variables, including heavy metals, explained more variation than a model developed using only mor layer thickness,pH, carbohydrate, ash and nitrogen concentrations, as independent variables. Thus there is a risk of toxic effects from Pb even at the levels found in south-western Sweden today(>120 g Pb * g dw^-1). However, since the correlationsbetween heavy metals and cellulose were not significantly different at the different sites, random sampling variation could not be ruled out as an explanation of the different results for the different sites. The causes of the correlationbetween organic matter quality and heavy metals have not yet been clarified. Analysis of mor samples incubated in thelaboratory for 2 yr with 1200 g Pb * g dw^-1 or 5 gHg * g dw^-1 did not show any differences in carbohydrate composition, compared to control samples. This shows that within-site studies of correlations between respiration rate and heavy metals have to be combined with studies of metal additions to soils and analysis of organic matter quality beforeany valid conclusions can be made.