机物料中溶解性有机质对土壤吸附除草剂的抑制作用

溶解性有机质(DOM)是陆地及水生生态系统中十分活跃的组分,对有机污染物质的环境行为 (如毒性、迁移转化及生物可降解性等)有着重要的影响,而施用有机物料会释放大量的DOM.采用批量平衡法研究了水稻秸秆腐解产生的溶解性有机质对苄嘧磺隆(BSM)在土壤中吸附行为的抑制作用.结果表明,线性方程能很好地描述BSM在土壤中的吸附行为;添加DOM降低了BSM在土壤中的分配系数即logKd值,其logKd值与对照(不加DOM)间存在极显著差异(P<0.01),秸秆腐解时间越长,logKd值越小;亲水组分和疏水组分在DOM抑制土壤吸附BSM中起着不同的作用;BSM在土壤上的吸附自由能小于40 kJ·mol-1,推测BSM在土壤上主要以物理吸附为主,吸附机理可能有范德华力、疏水键、氢键和偶极键力,不存在化学键吸附作用.     

Abiotic control on the dissipation of chlorpyrifos spiked in an Udic Ferrisol at a lower dosage

The dissipation routes of chlorpyrifos spiked in an Udic Ferrisol at the dosage of 400 ng g^?1, which represents a residual level after an agricultural application, were studied in a laboratory, using the natural soil under three moisture regimes, sterilised, and organic matter-free soils in the dark at 20°C. The obtained results showed that higher soil moisture caused faster dissipation, and the abiotic and biotic contributions to the total dissipated amount of the applied chlorpyrifos in the soil accounted for 77.3–85.2% and 14.7–22.7%, respectively. In the sterilised soil, the contribution of organic matter to chlorpyrifos dissipation was noticed to account for 95% in the earlier two weeks, and was nearly equal to that of soil minerals two weeks after the incubation.     

利用纤维二糖的酵母工程菌构建

以扣囊复膜孢酵母染色体DNA为模板,通过PCR方法扩增到其β-葡萄糖苷酶基因bgl1,经EcoRⅠ、BamHⅠ双酶切并和经相同酶切的穿梭表达载体pYX212连接,构建了重组质粒pYX-sbgl,转化酿酒酵母W 303-1A,bgl1基因获得了活性表达,β-葡萄糖苷酶活力为0.504 IU/mL.转化子能以纤维二糖为唯一碳源生长,并能应用于同时糖化和发酵纤维素底物生产乙醇,使乙醇产量较宿主酵母有了一定的提高.图6表1参14     

表面活性剂加强动电技术去除污泥中铜和镉

以实际城市污泥为研究对象,通过采用表面活性剂作为阴极液,并考虑阴极液pH值、表面活性剂类型和电压3种因素对动电技术去除污泥中重金属(铜和镉)的影响,选用正交试验确定最佳试验条件.结果表明,采用表明活性剂作为阴极液加强动电技术去除污泥中重金属足可行的,铜和镉的去除率分别达到11.1%～52.6%和9.1%～46.7%.通过对正交试验结果进行极差和方差分析,试验的最佳条件为:电压为20 V,阴极液加入十六烷基三甲基氯化铵并控制pH值为4～6.表面活性剂的类型对动电技术去除镉具有显著影响.其中,表面活性剂类型对动电过程的影响最大,阴极液pH值次之,电压影响最小.     

In situ iron activated persulfate oxidative fluid sparging treatment of TCE contamination--a proof of concept study

In situ chemical oxidation (ISCO) is considered a reliable technology to treat groundwater contaminated with high concentrations of organic contaminants. An ISCO oxidant, persulfate anion (S(2)O(8)(2-)) can be activated by ferrous ion (Fe(2+)) to generate sulfate radicals (E(o)=2.6 V), which are capable of destroying trichloroethylene (TCE). The property of polarity inhibits S(2)O(8)(2-) or sulfate radical (SO(4)(-)) from effectively oxidizing separate phase TCE, a dense non-aqueous phase liquid (DNAPL). Thus the oxidation primarily takes place in the aqueous phase where TCE is dissolved. A bench column study was conducted to demonstrate a conceptual remediation method by flushing either S(2)O(8)(2-) or Fe(2+) through a soil column, where the TCE DNAPL was present, and passing the dissolved mixture through either a Fe(2+) or S(2)O(8)(2-) fluid sparging curtain. Also, the effect of a solubility enhancing chemical, hydroxypropyl-beta-cyclodextrin (HPCD), was tested to evaluate its ability to increase the aqueous TCE concentration. Both flushing arrangements may result in similar TCE degradation efficiencies of 35% to 42% estimated by the ratio of TCE degraded/(TCE degraded+TCE remained in effluent) and degradation byproduct chloride generation rates of 4.9 to 7.6 mg Cl(-) per soil column pore volume. The addition of HPCD did greatly increase the aqueous TCE concentration. However, the TCE degradation efficiency decreased because the TCE degradation was a lower percentage of the relatively greater amount of dissolved TCE by HPCD. This conceptual treatment may serve as a reference for potential on-site application.     

Determination of Nitrobenzene in Wastewater Using a Hanging Mercury Drop Electrode

The determination of trace amount nitrobenzene in wastewater on a hanging mercury drop electrode was studied. The determination conditions of pH, supporting electrolyte, accumulation potential, accumulation time, and voltammetric response were optimized. The sharp peak of the nitrobenzene was appeared at 0.05 V. The peak electric current was proportional to the concentration of nitrobenzene in the range of 1.47 × 10⁻⁵ ∼ 1.0 × 10⁻³ mol/l with relative standard deviations of 3.99 ∼ 8.94%. The detection limit of the nitrobenzene in water was 5 × 10⁻⁶ mol/l. The proposed method offered low limit of determination, easy operation, the use of simple instrumentation, high sensitivity and good reproducibility. It was applied to the determination of nitrobenzene in wastewater with an average recovery of 94.0% ∼ 105%. The proposed method provided fast, sensitive and sometimes real time detection of nitrobenzene.     

土壤柴油污染修复的抽气提取去除实验研究

为得到土壤气相抽提(SVE)去除柴油的优化条件,进行了一维土柱抽气提取去除柴油污染物的实验研究,研究不同初始含水率、不同抽气量对污染土壤中柴油去除率的影响及不同深度残留柴油的变化规律。结果表明：在本实验模拟的范围内,抽气量越大,SVE处理效果越好;初始含水率越低,处理效果越好;此外,不同深度去除率变化的规律基本上是随深度的增大而减小。实验结果可为土壤轻油污染实际治理提供实验数据基础。     

江苏省一次典型沙尘污染过程分析

2021年4月16日至4月18日江苏省经历了一次受沙尘影响的重污染过程.本次过程沙源地为蒙古国中南部及中国内蒙古中西部地区,在蒙古气旋后部西北大风影响下,沙尘气团自西北向东南影响了中国多个省市和地区.江苏省自16日起逐渐受到沙尘过程影响,苏北城市ρ(PM10)从凌晨开始迅速升高,浓度最高达569μg/m3,空气质量达严...     

不同温湿度条件下微米硼的氧化过程研究

目的 探究不同温湿度条件下微米硼的氧化层结构特征。方法 利用高温水浴浸泡处理去除原料微米硼的表面氧化层,然后在恒温恒湿条件下对微米硼进行加速氧化,利用扫描电子显微镜、透射电子显微镜和X射线光电子能谱对加速氧化后硼颗粒的氧化层厚度及组成进行分析,总结表面氧化层结构及成分组成变化规律,揭示温湿度条件下微米硼的氧化机制。结果 微米硼经高温水浴浸泡处理后,表面氧化层去除率达到50%。随着加速氧化时间的延长,硼颗粒氧化层的厚度逐渐增大,由内向外硼颗粒表面可以用B-BxOy-B2O3三层结构来表示,BxOy总是伴随着B2O3同时出现的,且随着氧化反应的进行,颗粒表面BxOy的含量将超过B的含量。结论 不同温湿度条件下微米硼的氧化机制为O2向B颗粒内部单向扩散的反应机制,B先与O2反应,形成低氧化物BxOy,BxOy进而与O2反应生成B2O3。随着氧化层厚度的增加,O2向B颗粒内部扩散的阻力增大,氧化反应速率随之降低。相比湿度的影响,温度的升高可显著加快硼表面氧化层的形成;温度一定时,湿度的增加可促进硼氧化层的形成。     

UASB反应器处理染料及印染废水的研究进展

综述了国内外UASB反应器处理染料及印染废水的研究概况.分析了UASB反应器处理废水存在的问题,并给出了相应的建议.展望了UASB反应器处理染料及印染废水的发展趋势,指出厌氧UASB-好氧法组合工艺是目前处理染料及印染废水的一种经济而有效的方法.