HDNPTT与镉显色反应的研究

应用合成的新试剂 1- (2 -羟基 - 3 ,5 -二硝基苯 ) - 3 - (4 -苯基 - 2 -噻唑 ) -三氮烯 (HDNPTT) ,研究了在表面活性剂TritonX - 10 0存在下 ,它与Cd2 的显色反应。结果表明 ,在 pH 8 0～ 10 0范围内 ,Cd2 与该试剂形成的配合物 ,其最大吸收峰位于 5 35nm处 ,摩尔吸光系数为 1 89× 10 5L·mol-1·cm-1。Cd2 在 0mg/L～ 0 32mg/L范围内符合比尔定律。此法用于环境水样和人发样品中微量镉的测定 ,结果满意。     

2-(2-喹啉偶氮)-4-二乙氨基苯甲酸光度法测定镍的研究

合成了新试剂 2 -( 2 -喹啉偶氮 ) -4 -二乙氨基苯甲酸 ( QADEABA) ,并研究了其与镍的显色反应 ,在 p H=8.0的硼酸 -磷酸二氢钾缓冲介质中 ,吐温 -80存在下 ,QADEABA与镍反应生成 2∶ 1稳定络合物 ,λmax=5 90 nm ,ε=1 .1 8× 1 0 5L· mol-1· cm-1。镍含量在 0～ 0 .4 mg/ L内符合比耳定律 ,方法用于水样中镍含量的测定 ,结果令人满意     

均相催化强化US/FCME协同体系降解硝基苯

考察了NaCl、AlCl3、Na2SiO3、CuSO44种均相催化剂对超声波(US)/铁炭微电解(FCME)协同体系降解硝基苯的催化效果,结果表明,CuSO4的催化效果最好,在体系反应液初始pH为3.0,混合填料投加量为5.0 g/L(铁炭质量比为1∶1),CuSO4投加量为800 mg/L时,体系对硝基苯的降解率达到99.2%,但溶液COD值仅下降了24.6%,矿化效果一般,红外光谱分析表明降解体系的主要中间产物为苯胺。     

草酸钾活化法制备榴莲壳活性炭及其表征

以榴莲壳为原料,选择K2C2O4为活化剂,在自制氛围气中进行化学活化制备活性炭。考察了活化剂/原料浸渍比、活化温度与活化时间对活性炭的碘和亚甲基蓝吸附值及得率的影响。结果表明,制备榴莲壳活性炭的理想条件为:活化剂/原料浸渍比1.5∶1、活化温度800℃和活化时间120 min;此时活性炭的SBET(BET比表面积)、总孔容和微孔孔容分别为1 195 m2/g、0.60 cm3/g和0.41 cm3/g。利用比表面和孔隙度分析仪、场发射扫描电镜(FE-SEM)和傅立叶红外光谱法(FT-IR)对活性炭的孔结构特征、微观形貌和表面官能团进行了表征。FE-SEM观测结果显示榴莲壳活性炭孔隙结构发达,且含有丰富的中孔。     

临安区域本底站大气甲烷浓度变化特征

通过分析2006年8月～2009年7月临安区域大气本底站Flask瓶采样获得的CH4浓度特征,结合地面风向、后向轨迹、排放清单,研究了CH4浓度变化特征和长三角地区排放源对CH4浓度的影响作用。结果表明,临安区域大气本底站的CH4浓度分布在1 7584×10-9~1 9700×10-9,具有较明显的季节波动变化特征,浓度季节变化幅度为737×10-9;CH4浓度平均年增幅达176×10-9,增速较快。东北风和东南风时,CH4浓度较高;西南风时CH4浓度较低。导致CH4高浓度分布的气团主要来自临安站的东北、偏东方向;导致CH4低浓度分布的气团集中在西南 偏南     

Fe3O4／Ag磁性纳米颗粒去除水中的铅离子

采用水相共沉淀法制备小尺寸磁性Fe3O4纳米颗粒,以没食子酸作为还原剂和表面修饰剂,还原Ag[（NH3）2]’制备出Fe3O4／Ag磁性纳米颗粒。研究该磁性纳米颗粒对水溶液中铅离子的吸附行为,研究结果表明,pH为7．0,吸附温度30℃时可得到最好的处理效果,铅的去除率可达99．7％以上,Fe3O4／Ag颗粒吸附行为符合二级动力学模型（R2〉0．99）。该磁性纳米颗粒经过多次再生处理后,仍具有很好的吸附效果,表明Fe3O4／Ag在水处理方面拥有良好的应用前景。     

4-Ethylphenol and 4-ethylguaiacol in wines: Estimating non-microbial sourced contributions and toxicological considerations

Analyses of commercially available wines suggested non-Brettanomyces sources of 4-ethylphenol and 4-ethylguaiacol. Grapes, enological additions, exposure to plastics, and oak-barrel aging were potential inputs considered. Investigations of whole grape bunch samples from two major red wine Vitis vinifera cultivars (L. cv. Cabernet Franc and Pinot Noir), a commercial mannoprotein additive, and three commercial enological tannin additions indicated they are not likely significant sources of these compounds. Studies on 15 commercial oak barrelled red wines from six Vitis vinifera cultivars (L. cv. Cabernet Franc, Cabernet Sauvignon, Dunkelfelder, Merlot, Pinot Meunier, and Pinot Noir), and a review of volatile phenol extraction from toasted oak wood, suggested that oak-aging may produce concentrations of up to 50 μg L^?1 4-ethylphenol and 4-ethylguaiacol. Thus, following potential Brettanomyces-sourced aroma impacts in wine using 4-ethylphenol and/or 4-ethylguaiacol concentrations as proxies should only be considered reliable at analyte levels > 100 μg L^?1. A review of worldwide 4-ethylphenol and 4-ethylguaiacol concentrations in wine, consumption patterns, and available toxicological data also suggested that levels of 4-ethylphenol being observed in wines worldwide do not warrant concerns about acute or long-term effects. While little is known about the toxicology of 4-ethylguaiacol, it is unlikely that elevated concentrations will pose any health-related concerns.     

Comparison of surface emissions and subsurface distribution of cis- and trans-1,3-dichloropropne and chloropicrin in sandy field beds covered with four different plastic films

The purpose of this study was to conduct a field study at a Florida field site on surface emissions and subsurface distribution of cis-and trans-1,3-dichloropropene (1,3-D) and chloropicrin (CP) in raised beds injected with Telone C35 with four replications. A total of 16 beds were applied with Telone C35 by chisel injection and covered with four different plastic films, 4 beds for each film. Each bed was installed with five 20-cm long soil pore air probes and a surface air collection pan at arbitrarily locations along the length of each bed for sampling soil pore air and surface air, respectively, for analysis of the three biologically active compounds, cis- and trans-1,3-D and CP. We found that average concentrations of the three compounds at 20-cm depth among the beds covered with four different plastic films generally were not statistically different. Among the four beds covered with the same plastic film, average concentrations of the three compounds were statistically different only in the four metallic PE covered beds at 5 and 24 hours after injection. Volatilization rates of the three compounds among the beds covered with four different plastic films, with the exception of CP at 48 hours after injection, were not statistically different. It appeared that initial upward diffusion and volatilization flux were influenced by solar radiation. Initial subsurface concentrations of the three compounds and volatilization flux, especially cis-1,3-D, were greater in the beds on the east side of the field than that in the beds on the west side of the field. Whether or not difference in initial subsurface concentrations of the compounds between east side beds and west side beds may influence fumigant efficacy remains to be determined.     

两相厌氧消化工艺处理鸡粪

以鸡粪为发酵原料,采用序批式两相厌氧消化工艺在中温条件(37℃)下对其进行消化处理。分别将水解酸化相和产甲烷相pH值控制在5.5±0.3和7.0±0.3,通过改变进样含固率(TS)研究有机负荷(OLR)对两相消化系统处理鸡粪过程中污染物转化和去除效果的影响。结果表明,水解酸化相出水总有机碳(TOC)、挥发酸(VFAs)和氨氮(NH4+-N)浓度都随OLR升高而升高。VFAs组成相对稳定,其中乙酸占总VFAs浓度的57%～64%,其次为正丁酸和丙酸。产甲烷相出水TOC和VFAs稳定在较低水平,TOC去除率最大达到90%以上。产甲烷相进水氨氮主要以NH4+形式在反应器内不断积累。实验后期产甲烷相生物气中甲烷体积分数维持在64%上,证明两相消化系统在实验条件下良好运行。     

产酸克雷伯氏菌Klebsiella oxytoca对硝基苯及4-氯硝基苯的降解

硝基苯类化合物生物降解菌的筛选及性能研究,是制药、染料等行业废水达标的重要基础。以浓度梯度升高法筛选到一株硝基苯厌氧降解菌Klebsiella oxytoca NBA-1。考察了该菌对氧气的需求,以及在厌氧条件下,温度、pH值、外加葡萄糖及硝基苯初始浓度等环境因子对菌株降解硝基苯能力的影响,并进一步讨论菌株对氯取代硝基苯类化合物的降解情况。结果表明,该菌在厌氧条件下生长比好氧条件下慢,但降解速度更快;厌氧降解硝基苯的最佳pH值和温度和分别为8.3和30~35℃;加入0.3%~0.5%的葡萄糖可促进降解,且对300 mg/L以下的硝基苯均有降解能力;该菌能将4-氯硝基苯转化为4-氯苯胺,并进一步脱氯为苯胺。研究结果可为硝基苯及含氯硝基苯的处理工艺选择提供相关的参考依据。