Extractable atrazine and its metabolites in agricultural soils from the temperate humid zone

Extractable atrazine and its metabolites (hydroxyatrazine, deethylatrazine and deisopropylatrazine) were evaluated in agricultural soils from the temperate humid zone (Galicia, NW Spain) under laboratory conditions. The experiment was performed with five soils with different properties (organic C, soil texture and atrazine application history), both unamended and treated with atrazine at field application rate. Measurements of the atrazine compounds were made at different time intervals (1, 3, 6, 9 and 12 weeks) during a 3-month incubation period. Results showed that only hydroxyatrazine was detected in the extractable fraction of the unamended soils, with values remaining relatively constant throughout the incubation period. Atrazine addition notably increased the concentration of the parent compound and its degradation products; deisopropylatrazine and hydroxyatrazine were the main metabolites detected in the extractable fraction of the treated soils, whereas deethylatrazine was not detected. After 7 days incubation, values of total extractable residues, expressed as percentage of initially added atrazine, ranged from 75 to 86% (25–68% of atrazine, 7–11% of hydroxyatrazine and 9–57% of deisopropylatrazine). The values decreased rapidly during the first 3 weeks of incubation, showing values of 2–8% in soils with higher atrazine application and from 28 to 30% in soils with lower application history. At the end of the incubation, 2–8% of total extractable residues were still detected (0–4% of atrazine, 2–3% of hydroxyatrazine and 0–2% of deisopropylatrazine), indicating a residual effect of atrazine addition. These variations in the extractable fraction indicated that most added atrazine was rapidly degraded, especially in soils with higher application history.     

不同粒径垃圾焚烧飞灰重金属分布和浸出性质

对烟气净化系统飞灰(以下简称飞灰)按粒径进行分级,研究了飞灰重金属含量、形态分布和浸出毒性随粒径的变化,讨论了不同粒径的飞灰对重金属总量和浸出总量的贡献率.结果表明:飞灰中粒径>154 μm和<30 μm的颗粒较少,粒径为38.5～74 μm的颗粒约占总量的50%.除Ni和Cr外,重金属含量随飞灰粒径的减小呈增加趋势,且主要表现在酸溶态Cd,Zn,Pb,Cu和有机结合态Pb以及晶形氧化铁态Pb,Zn含量的增加.随着飞灰粒径的减小,Cr,Ni,Zn,Hg和Pb的浸出量也呈逐渐增加趋势,其中Zn,Hg和Pb的表现尤为突出.尽管细颗粒上的重金属对飞灰的重金属总量贡献不大,但高浸出率使细颗粒飞灰对重金属浸出总量仍具有较大贡献,尤其是Pb,Zn和Hg,在占飞灰质量8%的粒径<30 μm的飞灰中,富集了约40%的水溶性Pb,Zn和Hg.      

湿式提砷法在处理工业废水及废渣中的应用

采用硫化法去除冶金工业酸性废水中的砷．除砷形成的含砷（ 主要成分 As₂S₃） 废渣用浓硫酸处理,废渣中的砷元素以 As₂O₃ 形式回收,纯度达99.4 ％ ,同时回收副产物硫磺等．试验结果表明,该方法的化学反应速度快,工艺过程稳定,砷的总回收率达95 ％ 以上,除砷效率可达99.99 ％ ．     

宁波市鄞州区农作物农药残留现状与控制对策

对鄞州区种植的稻谷、叶菜类、水果类、豆类、茄果类和块茎类农产品按月进行了411个批次抽样,按照国家相关规定对22个农药项目进行了检测。检测结果发现样本农药项目检出率为0.3%,农产品农药残留合格率97.82%,农药残留检出项目中88.89%是杀虫剂。超出农药残留标准的样本主要是5-10月的青菜,叶菜类超标样本率达到3.72%。农药残留超标样本在平原、滨海地区种植散户中有发现,而在山区各规模农户中均有发现。小学文化程度农户样本农药残留超标率高达4.50%,是大学文化程度农户样本农药残留超标率的6.16倍。为了降低鄞州区农作物农药残留率,提出5方面的控制对策。     

Role of dissolved humic acids in the biodegradation of a single isomer of nonylphenol by Sphingomonas sp

This study shows the important role of humic acids in the degradation of ¹⁴C and ¹³C labeled isomer of NP by Sphingomonas sp. strain TTNP3 and the detoxification of the resulting metabolites. Due to the association of NP with humic acids, its solubility in the medium was enhanced and the extent of mineralization of nonylphenol increased from 20% to above 35%. This was accompanied by the formation of significant amounts of NP residues bound to the humic acids, which also occurred via abiotic reactions of the major NP metabolite hydroquinone with the humic acids. Gel permeation chromatography showed a non-homogenous distribution of NP residues with humic acids molecules, with preference towards molecules with high-molecular-weight. Solid state ¹³C nuclear magnetic resonance spectroscopy indicated that the nonextractable residues resulted exclusively from the metabolites. The chemical shifts of the labeled carbon indicated the possible covalent binding of hydroquinone to the humic acids via ester and possibly ether bonds, and the incorporation of degradation products of hydroquinone into the humic acids. This study provided evidences for the mediatory role of humic acids in the fate of NP as a sink for bacterial degradation intermediates of this compound.     

有机磷酸HEDP稳定垃圾焚烧飞灰重金属的研究

研究了有机磷酸羟基亚乙基二膦酸（HEDP）对生活垃圾焚烧飞灰中重金属的稳定方法.通过对不同HEDP投加量处理后的飞灰试样作危险废物浸出毒性鉴别试验,分析HEDP最佳使用剂量,并评价了稳定化飞灰的长期稳定性.结果表明,HEDP最适使用剂量为0.03 Ml/g（以商品级HEDP与飞灰的体积质量比计）,处理后飞灰与原状飞灰相比,Pb、Zn和Hg的浸出浓度分别降低了98.3%、99.5%和85.0%.HEDP对飞灰中重金属稳定效果排序为：Pb＞Zn＞Hg＞Ni＞Cu＞Cd＞CrHAs.重金属pH相关浸出测试（pH-dependent leaching tests）表明：经0.03mL/g HEDP稳定处理的飞灰,在0.3 mol/L HNO3和0.3 mol/L NaOH的浸取条件下,其重金属浸出浓度均低于国家危险废物鉴别标准,显示具有良好的长期稳定性.     

城市有机生活垃圾厌氧发酵处理研究

在适当的PH值和搅拌条件下，研究了反应温度、总固体含量、pH值、碳氮比、碳磷比以及接种物量对有机牛活垃圾厌氧发酵产沼气的影响。实验结果表明：有机生活垃圾厌氧消化产沼气的适宜条件是：反应温度50～55℃，总固体含量23％～28％，pH=6．8～7．4，w(C)／w（N)=(20～30)，w(C)／w(P)=50，60％～75％的生物气，可实现能量回收；发酵剩余物可制有机肥，时间为15～20d。接种物量为25％～30％。在厌氧的条件下，可以制取含甲烷实现物质再利用。有机生活垃圾在厌氧消化反应器的停留时间为15～20d。     

多环芳烃在全土及其碱提残余物上的吸附行为

以菲和芘为代表性化合物,采用8种有机质含量不同的天然全土样品及其碱提残余物进行吸附实验,并利用不同吸附模型进行数据拟合,藉以探讨有机质含量对土壤吸附行为的影响.结果表明,Freundlich吸附模型的非线性指数n都小于1,显示全土和碱提残余物在多环芳烃的吸附过程中表现出非线性特征.菲和芘的吸附行为随土壤有机质含量不同而变化,碱提残余物的吸附能力强于全土,两者吸附行为的差异主要归因于土壤有机质含量和性状的区别.     

Incorporation of pesticides by soil micro-organisms as a way of bound residues formation

We studied the ¹⁴C-tagged biochemical compartments such as proteins, lipids and polysaccharides from bacterial and fungal cultures supplied with ¹⁴C-pesticides and ¹⁴C-glucose. We showed that ¹⁴C incorporation depends both on the substrate structure and on the nature of the micro-organism. Both bacterial and fungal cells incorporated glucose ¹⁴C mainly into cell wall proteins. By contrast, glyphosate ¹⁴C was mainly incorporated into cytoplasm carbohydrates by fungi. On the other hand, 2,4-dichlorophenoxyacetic acid ¹⁴C was mainly found in the carbohydrate fractions of the bacteria walls.