兼氧接触工艺处理造纸中段废水中间试验的研究

采用中试规律的兼氧接触工艺处理造纸中段废水，当处理水量为４．８ｍ＾３／ｄ，水力停留时间３～４ｈ，气水比３：１，进水ＰＨ８～９．５，平均ＣＯＤ浓度为１６４１．６ｍｇ／ｌ，ＢＯＤ５５１６．１ｍｇ／ｌ，ＳＳ６８８．４ｍｇ／ｌ的条件下，处理后出水ｐＨ７．５左右，平均ＣＯＤ浓度为１０５９．８ｍｇ／ｌ，去除率３４．９％，ＢＯＤ５２４６．５ｍｇ／ｌ，去除率５２．１％，ＳＳ１６１．９ｍｇ／ｌ，去除率为７７．１％。     

小型CAF气浮设备处理滇池含藻水的试验研究

采用自制的小型涡凹型气浮(CAF)设备处理滇池含藻水，结果表明，在气浮时间为1min，分离时间为6min的条件下，聚硅硫酸铁铝(PFASSI)用量为40mg／L时，对藻类和浊度的净化效率最大分别为80．1％和78．6％；在聚丙烯酰胺(PAM)的用量为2mg／L时，对藻类和浊度的净化效率分别为95．9％和93．2％。使用PFASSI(20mg／L)和PAM(1mg／L)的组合絮凝剂时，滇池含藻水的含藻量由557mg／L降到5．57mg／L，浊度由375度降到27度，二者的去除率分别为99％和92．8％。     

2种新分离微藻的生长、氮磷去除和营养特性的比较研究

为了解2种新分离微藻的净化和资源化潜力，研究比较了其生长、氮磷去除和营养特性。结果表明，栅藻和月牙藻的最大生物量（干重）分别为0．78g／L和0．53g／L；最大生物量（干重）增长速率分别为0．05g／（L·d）和0．03g／（L·d）。培养至第23天，栅藻和月牙藻对TN的去除率分别为85．1％和72．5％；对TP的去除率为82．6％和79．7％，但栅藻较月牙藻更易释放较多的No2--N进入藻液。稳定期时，栅藻、月牙藻的粗蛋白质含量和粗蛋白产量（干重）分别为31．8％、19．2％和0．24g／L、0．09g／L；粗脂含量和粗脂产量（干重）分别为7．81％、9．26％和0．06g／L、0．05g／L。综上，与月牙藻相比，栅藻具有明显的生长、氮磷去除和营养优势，在进行水产养殖废水的净化和资源化利用上可作为优选藻种。     

A／O-MBR工艺处理校园生活污水中水回用工程的设计与运行

针对Et处理量为1500m3的高校中水处理设施，论述了缺氧／好氧-MBR（A／O—MBR）处理工艺运行特性，完成了长效监测及经济性评价。系统MBR池污泥浓度（MLSS）控制在8～12g／L，缺氧池和好氧池水力停留时间（HRT）分别为3h和7h，污泥回流比为200％～300％。当进水COD、总氮、氨氮平均浓度分别为481．3、75．1和65．8mg／L时，出水COD、总氮、氨氮平均浓度分别为16．5、13．4和0．7mg／L，平均去除率分别为96．4％、81．9％和99．0％。在进行化学除磷的情况下，出水总磷的平均浓度为0．8mg／L，平均去除率86．5％。出水水质优于《城市污水再生利用城市杂用水水质》（GB／T18920—2002）中的相应水质指标要求。经济性分析结果显示，该中水站的电耗为0．58kWh／m3。     

太湖梅粱湾水体中阿特拉津的毛细管气相色谱法测定

固相萃取（SPE）技术结合毛细管气相色谱（GC-μECD），测定了饮用水源地太湖梅粱湾水体中内分泌干扰物阿特拉津的含量，并用GC-MS进一步验证了分析结果。检测下限为10ng／L，方法回收率为75．58％～97．79％，RSD为0．38％～4．50％，在10ng／L-3640μg／L保持线性，其线性相关系数为0．9994。太湖梅梁湾水体中阿特拉津质量浓度在21．3～613．9ng／L，污染来源可能为太湖周围的农作区。     

水葫芦对萘的降解作用研究

分别在静态和动态两种条件下，以水葫芦为对象，对水生植物净化塘处理萘污水进行研究。结果表明，在静态试验中，水葫芦净化塘对浓度为2．5、6．5和16．1mg／L萘污水的7d净化率分别为97．1％、93．7％和90．4％。动态试验中，相同浓度萘污水7d后的出水净化效率分别为99．2％—99．9％、97．3％—98．6％和94．6％—96．7％。进水浓度分别为1．2mg／L和6．5mg／L萘污水在水葫芦净化塘中的最佳停留时间分别为5d和7d，水葫芦净化塘动态过程的净化效率高于静态过程。     

潜流人工湿地-生物接触氧化处理低温低浓度生活污水

在低温低浓度生活污水的实验研究中，回流比和气水比是影响潜流人工湿地一生物接触氧化组合工艺污染物去除效果的重要因素，推荐回流比R=1．0，气水比为4：1，在该工况下，进水COD浓度在170．8～221．3mg／L时，平均去除率可达90％；进水NH3-N浓度在17．3～25．9mg／L，平均去除率45％～65％；进水TN浓度在25．1～38．49mg／L时，平均去除率45％～65％；进水TP浓度在2．2～3．1mg／L时，平均去除率65％～80％。污染物沿程浓度分析结果表明，该组合工艺可以在低温季节通过曝气促进氨氮硝化，大幅提高NH3-N和TN去除率，同时可以充分发挥复合潜流湿地功能。     

车间空气中三甲胺的气相色谱测定

提出了一种快速，灵敏的车间空气中三甲胺的测定方法，在２．５￣１０ｍｇ／ｍ＾３范围内回收率为９３．６％￣１１０．６８％，变异系数５．６％，最低检出限为１μｇ／ｍＬ，二甲胺和氨对其均无干扰。     

高效液相色谱法测定废水中的辛硫磷、毒死蜱

建立了HPLC法测定废水中辛硫磷及毒死蜱的方法，优化了检测波长、溶剂、流动相等试验条件。辛硫磷、毒死蜱在0．050—1．000mg／L范围内线性良好，检出限为0．0033～0．0045mg／L，RSD为2．2％-4．1％，加标回收率为97．4％～105％。     

间隔流动分析仪测定水中的挥发酚

介绍了间隔流动分析仪测定水中挥发酚的分析方法，实验结果表明，有证标样的测定值均在其保证值范围内，相对标准偏差为0．9％～1．4％，检出限为0．001mg／L，加标回收率在92．5％-110％之间，精密度和准确度良好，且分析速度达20个／h。     

Analytical methods for the determination of alachlor, metolachlor, simazine and atrazine mobility in soils

A method for the determination of the mobility of the herbicides, alachlor, metolachlor, simazine and atrazine in soil is described. The method is based on the use of soil thin-layer chromatography (TLC) and does not require the use of radiolabelled compounds. Soil on the TLC plate after development was separated into various bands, the material in each band was extracted with solvents and analyzed by gas chromatography.     

Analytical methods for the determination of alachlor,metolachlor, simazine and atrazine mobility in soils

Abstract

A method for the determination of the mobility of the herbicides, alachlor, metolachlor, simazine and atrazine in soil is described . The method is based on the use of soil thin‐layer chromatography (TLC) and does not require the use of radiolabelled compounds. Soil on the TLC plate after development was separated into various bands, the material in each band was extracted with solvents and analyzed by gas chromatography.     

Combined effect of microwave and activated carbon on the remediation of polychlorinated biphenyl-contaminated soil

The application of microwave and activated carbon for the treatment of polychlorinated biphenyl (PCB) contaminated soil was explored in this study with a model compound of 2,4,5-trichlorobiphenyl (PCB29). PCB-contaminated soil was treated in a quartz reactor by microwave irradiation at 2450MHz with the addition of granular activated carbon (GAC). In this procedure, GAC acted as microwave absorbent for reaching high temperature and reductant for dechlorination. A sheltered type-K thermocouple was applied to record the temperature rising courses. It was shown that the addition of GAC could effectively promote the temperature rising courses. The determination of PCB residues in soil by gas chromatography (GC) revealed that rates of PCB removal were highly dependent on microwave power, soil moisture content, and the amount of GAC added. GC with mass spectrum (MS) detector and ion chromatography were employed for the analysis of degradation intermediates and chlorine ions, respectively. It was suggested that microwave irradiation with the assistance of activated carbon might be a potential technology for the remediation of PCB-contaminated soil.     

加油站场地油品渗漏探测及土壤污染评估

用洛阳铲采集某地区10座地下贮罐罐龄接近或超过10年的典型加油站场地不同深度土样,并分别用吹脱/捕集/热脱附/气相色谱法和快速溶剂萃取/硅酸镁净化/气相色谱法分析样品中的挥发性和萃取性石油烃,发现2座加油站疑似油品渗漏,其中1座为柴油渗漏,地下贮罐附近1.2 ～3.0 m深度土壤总石油烃含量16.1 ～24.6 g/kg,均超过荷兰土壤清除标准,另1座为汽油和柴油混合渗漏,其地下贮罐附近2.4m深度土壤总石油烃含量较高,但未超标.个别加油站场地较高的土壤天然有机物背景值可能计入EPH的分析结果,但其色谱指纹明显不同于石油烃.     

Behavior of triadimefon in two Lebanese soils.

The retention and fate of triadimefon fungicide were studied under two environmental conditions. Field studies were conducted on two soils, a sandy loam soil (Fanar) and a clay soil (Raouda). Fanar is a wet coastal area while Raouda is a dry agricultural area of the Bekaa plain located at an elevation of 870 m above sea level. Triadimefon was applied with a jet sprayer at 267 g a.i.ha(-1) and 200 g a.i.ha(-1) at Fanar and Raouda, respectively. Reconstituted soil columns (600 x 30 mm) glasses, were used to study the fungicide movement and metabolism in the two soils. Analyses of triadimefon and its metabolites were carried out using gas chromatography (GC) and high performance liquid chromatography (HPLC). The results indicated a weak reversibility of the adsorbed fraction in the clay soil. Clay is considered an important factor in triadimefon adsorption. Triadimefon mobility in the sandy-loam soil was relatively high in comparison with behavior in the clay soil where about half of the applied fungicide was detected in the upper 25 cm of soil, six days after treatment. Rapid degradation of triadimefon to triadimenol was observed in the two soils. The observed half-life was 8 days in sandy-loam and 13 days in clay soils.     

Fate of chlorophenoxyacetic acids in acid soil

The relative persistence of MCPA, 2,4-D and 2,4,5-T in an acid soil was assessed under laboratory conditions with field capacity and flooded level of soil moisture. The experimental soil was incubated for 96 weeks and samples were collected at a specific interval for the determination of the residues by the gas chromatography. The decomposition was faster with MCPA than those of 2,4-D and 2,4,5-T. Soil moisture affected the degradation rate sharply.     

Analysis of herbicide Krovar I by liquid chromatography with atmospheric pressure chemical ionization mass spectrometry

A simple, very efficient method is presented for routine analysis of herbicide Krovar I (active components bromacil and diuron) in water and soil samples. Water samples were extracted by liquid-liquid extraction with dichloromethane (DCM) as extraction solvent. For soil samples two different extraction techniques were compared: microwave-assisted solvent extraction and a shaking technique using a platform shaker. Extracts were analyzed by high performance liquid chromatography using a water:methanol gradient. Liquid chromatography was coupled with atmospheric pressure chemical ionization mass spectrometry (LC-APCI-MS) for quantification of bromacil and diuron. Optimization of the APCI-MS was done by using standards in the flow injection analysis mode (FIA). Method detection limit for liquid samples for bromacil is 0.04 microg L(-1) and for diuron 0.03 microg L(-1). Method detection limit for soil samples is 0.01 microg g(-1) dry weight for both compounds. Results of analysis of field samples of water and soil are also presented.     

Influence of soil type and extraction conditions on perchlorate analysis by ion chromatography

Perchlorate is a stable anion that has been introduced into the environment through activities related to its production and use as a solid rocket propellant. Perchlorate is thought to transport through soils without being adsorbed; thus, for determination of perchlorate in soil, samples are typically extracted with water prior to analysis. The completeness of extraction depends on perchlorate existing as a free ion within the soil matrix. In this study, perchlorate extraction efficiency was evaluated with five soil types under two different oxygen states. For each soil, 30% (w/w) slurries were prepared and equilibrated under either oxic or anoxic conditions prior to spiking with a stock solution of sodium perchlorate, and the slurries were then maintained for 1-week or 1-month. At the end of the exposure, slurries were centrifuged and separated into aqueous and soil phases. After phase separation, the soil was washed first with deionized water and then with 50mM NaOH, producing second and third aqueous phases, respectively. Perchlorate concentrations in the three aqueous phases were determined using ion chromatography. The results obtained from this study suggest that matrix interference and signal suppression due to high conductivity have greater effects upon observed perchlorate concentrations by ion chromatography than does perchlorate interaction with soil. Thus, a single water extraction is sufficient for quantitative determination of perchlorate in soil.     

丙溴磷在稻田环境中的残留动态研究

确立了气相色谱法测定丙溴磷残留量的检测方法.采用该方法,丙溴磷在土壤、植株、糙米、稻壳和田水中的平均添加回收率为87.2％～103.6％,变异系数为3.20％～11.50％,最低检测质量浓度:田水为0.005 mg/kg;土壤、植株、糙米和稻壳为0.050 mg/kg.残留动态研究表明,丙溴磷在田水、植株和土壤中的半衰...     

Analysis of Herbicide Krovar I™ by Liquid Chromatography with Atmospheric Pressure Chemical Ionization Mass Spectrometry

Abstract

A simple, very efficient method is presented for routine analysis of herbicide Krovar I? (active components bromacil and diuron) in water and soil samples. Water samples were extracted by liquid–liquid extraction with dichloromethane (DCM) as extraction solvent. For soil samples two different extraction techniques were compared: microwave-assisted solvent extraction and a shaking technique using a platform shaker. Extracts were analyzed by high performance liquid chromatography using a water:methanol gradient. Liquid chromatography was coupled with atmospheric pressure chemical ionization mass spectrometry (LC-APCI-MS) for quantification of bromacil and diuron. Optimization of the APCI-MS was done by using standards in the flow injection analysis mode (FIA). Method detection limit for liquid samples for bromacil is 0.04 µg L^?1 and for diuron 0.03 µg L^?1. Method detection limit for soil samples is 0.01 µg g^?1 dry weight for both compounds. Results of analysis of field samples of water and soil are also presented.