火炸药生产废水污染土壤修复的研究进展

总结了国内外化学修复法和生物修复法修复火炸药生产废水污染土壤的研究进展。比较了各种方法的优缺点,提出了未来火炸药生产废水污染土壤修复技术的研究方向。指出:应将物理修复法、化学修复法及生物修复法相结合,将修复定位于综合化、彻底化及可利用化,以期达到火炸药生产废水污染土壤的无害化治理。     

多环芳烃典型电子性质与其大型蚤光致毒性的构效关系研究

多环芳烃(PAHs)是环境中广泛分布的持久性有毒有机污染物,备受研究者关注。基于密度泛函理论(DFT)先期计算PAHs前线分子轨道能隙可能与其光致毒性诱发所需吸收光照辐射能有一致性,本研究选取非取代PAHs对大型蚤(Daphnia magna)光致毒性实验数据,通过DFT计算典型电子性质,由偏最小二乘(PLS)分析方法优化发展了定量构效关系模型,经与前人结果比较和验证其拟合优度、稳定性和内外部预测性能均有显著提升,可在应用域(AD)范围内准确预测PAHs光致毒性而满足风险评估需求。构效关系分析结果表明,PAHs光致毒性与分子前线轨道能隙紧密相关,除苯并[k]荧蒽和屈可能具有不同的光致毒性作用机制之外,多数PAHs若具有较低的前线轨道能隙、较小分子稳定性和较大分子变形性,均将有利于促进其光致毒性作用的发生;结合PAHs光致毒性与分子前线轨道能隙间的相关关系,可推测DFT计算前线轨道能隙宽度在2.740~4.208 e V之间和对应光照辐射波段约为295 nm~450 nm时,PAHs污染暴露将可能诱发较高的光致毒性效应。这为太阳光照射下PAHs光致毒性作用机制阐释和风险评价提供了数据支持与理论依据。     

菲和铬(Ⅵ)单一及复合暴露对土壤微生物多样性的影响

有机物和重金属已成为我国土壤环境中常见的2类污染物质,二者间复合污染引起的土壤生态环境风险不容忽视。本研究以多环芳烃模式物菲和典型重金属铬(VI)作为受试物质,采用PCR-DGGE分子指纹图谱技术,探讨这2种污染物单一及复合暴露对土壤微生物群落多样性的影响,并选用主成分分析、聚类分析和戴斯系数3种算法对微生物群落相似性进行了比较。结果表明,在暴露实验第1天,菲单一暴露低浓度组中微生物群落相似性产生了极为明显的变化,而到第7天时,菲和铬(VI)单一暴露高浓度组均对微生物群落结构相似性产生最大程度的影响;采用香农指数法评价微生物群落的多样性,发现在暴露实验第7天,菲和铬(VI)单一暴露高浓度组对微生物群落多样性的影响比复合暴露高浓度组更强,二者复合暴露的相互作用方式表现为拮抗效应。本研究证明低浓度菲短期暴露的效应高于高浓度暴露结果,因而多环芳烃菲自身及其在复合暴露中所扮演的角色尤其值得关注。     

膜法处理含油废水研究进展

介绍了含油废水的来源、危害及其一般的处理方法,概述了国内外处理含油废水的膜分离技术——微滤、超滤、反渗透及膜法联合处理工艺的研究现状。对膜污染与预防问题进行了探讨,指出了膜法联合处理工艺是今后处理含油废水的研究方向,而研制抗污染、净化效果好、成本低廉的新型功能有机高分子过滤吸附材料也是含油废水处理领域的一项重要工作。     

超声波处理剩余活性污泥促进厌氧消化

用超声波处理剩余活性污泥(简称污泥),考察了污泥絮体结构、污泥中溶解性化学需氧量(SCOD)的变化规律及超声波处理对污泥厌氧消化的影响。实验结果表明,声强大于1 040W/m2时,用超声波处理污泥30m in以上,污泥絮体被打碎,污泥絮体结构遭到严重破坏,污泥中SCOD迅速增加,加速了污泥中有机质的水解反应;声强为2 000W/m2时,用超声波处理污泥60m in,中温((37±1)℃)厌氧消化10d,COD去除率为41%;厌氧消化25d的总产气量比未经超声波处理的污泥总产气量提高了53%;将发酵罐容积放大10倍,经超声波处理的污泥25d累积的总产气量比未经超声波处理的污泥总产气量提高了约25%。     

废水生物处理出水中溶解性微生物产物的形成机制与特征

废水生物处理出水中的溶解性微生物产物(SMP)主要产生于基质降解和微生物的内源呼吸过程,它的存在是影响生物处理出水水质和有机物去除率的一个重要因素,已引起人们的普遍关注.简单阐述了SMP的定义,详细探讨了废水生物处理出水中溶解性微生物产物的形成机制与特征.     

生态足迹计算模型应用中热点问题及探讨

简要介绍了生态足迹计算模型,论述了近年国际上争论的几个主要热点问题,数据的准确完整性,初级产品与二级产品,均衡因子与产量因子,全球产量与本地产量,以及能源足迹计算等,并对其进行了探讨和指出今后研究发展的方向。     

Laser-induced breakdown spectroscopy application in environmental monitoring of water quality: a review

Water quality monitoring is a critical part of environmental management and protection, and to be able to qualitatively and quantitatively determine contamination and impurity levels in water is especially important. Compared to the currently available water quality monitoring methods and techniques, laser-induced breakdown spectroscopy (LIBS) has several advantages, including no need for sample pre-preparation, fast and easy operation, and chemical free during the process. Therefore, it is of great importance to understand the fundamentals of aqueous LIBS analysis and effectively apply this technique to environmental monitoring. This article reviews the research conducted on LIBS analysis for liquid samples, and the article content includes LIBS theory, history and applications, quantitative analysis of metallic species in liquids, LIBS signal enhancement methods and data processing, characteristics of plasma generated by laser in water, and the factors affecting accuracy of analysis results. Although there have been many research works focusing on aqueous LIBS analysis, detection limit and stability of this technique still need to be improved to satisfy the requirements of environmental monitoring standard. In addition, determination of nonmetallic species in liquid by LIBS is equally important and needs immediate attention from the community. This comprehensive review will assist the readers to better understand the aqueous LIBS technique and help to identify current research needs for environmental monitoring of water quality.     

Application of portable gas chromatography-photo ionization detector combined with headspace sampling for field analysis of benzene, toluene, ethylbenzene, and xylene in soils

A method based on headspace (HS) sampling coupling with portable gas chromatography (GC) with photo ionization detector (PID) was developed for rapid determination of benzene, toluene, ethylbenzene, and xylenes (BTEX) in soils. Optimal conditions for HS gas sampling procedure were determined, and the influence of soil organic matter on the recovery of BTEX from soil was investigated using five representative Chinese soils. The results showed that the HS-portable-GC-PID method could be effectively operated at ambient temperature, and the addition of 15 ml of saturated NaCl solution in a 40-ml sampling vial and 60 s of shaking time for sample solution were optimum for the HS gas sampling procedure. The recoveries of each BTEX in soils ranged from 87.2 to 105.1 %, with relative standard deviations varying from 5.3 to 7.8 %. Good linearity was obtained for all BTEX compounds, and the detection limits were in the 0.1 to 0.8 μg kg^?1 range. Soil organic matter was identified as one of the principal elements that affect the HS gas sampling of BTEX in soils. The HS-portable-GC-PID method was successfully applied for field determination of benzene and toluene in soils of a former chemical plant in Jilin City, northeast China. Considering its satisfactory repeatability and reproducibility and particular suitability to be operated in ambient environment, HS sampling coupling with portable GC-PID is, therefore, recommended to be a suitable screening tool for rapid on-site determination of BTEX in soils.     

Spatial, temporal, and speciation variations of heavy metals in sediments of Nan'ao Island, a representative mariculture base in Guangdong coast, China

Heavy metals in sediments from Baisha Bay, Nan'ao Island, one of Guangdong Province's largest mariculture bases in Southern China, were investigated. The results display that the concentrations of 6 heavy metals from surface sediments were 0.040-0.220 (Cd), 24.22-39.61 (Pb), 25.30-42.66 (Cr), 10.83-19.54 (Ni), 15.06-39.24 (Cu) and 55.12-141.73 mg kg(-1) (Zn), respectively. The highest concentrations and the greatest increasing rates of heavy metals were found in a sediment core in a fish cage culture area due to receiving sewage discharge, uneaten fish bait, and boat gasoline combustion. Cd was preferentially associated with the acid-soluble fraction and Pb mainly with the reducible fraction in surface sediments. Meanwhile, Cd and Pb displayed greatest labile fractions, indicating anthropogenic origin. A principal component analysis (PCA) revealed three groupings (Cd; Cr, Ni and Cu; Pb and Zn) that mainly result from different distributions of the metals in the various fractions. The ecological risk of the polluted sediments stemmed mainly from Cd, and from Pb and Cu to a lesser degree. It is suggested that the density of fish-stocking be controlled, periodic movement of rafts (cages) be introduced, and the total numbers of net-cages and human activities in the mariculture zones be restricted. in order to facilitate the recovery of the polluted sediment.