快速溶剂萃取-分子筛脱水净化-气质联用法测土壤有机氯农药

用丙酮和正己烷(体积比为1∶1)作溶剂,在100℃和1 500 psi的压力下,用快速溶剂萃取仪从土壤中萃取出有机氯农药,用分子筛进行脱水和净化,GC-MS进行分析,对土壤中有机氯农药进行测定。方法的检出限为0.000 4~0.000 7 mg/kg,曲线的相关系数在0.998以上。对进口标准土进行测定,回收率为77.1%~105.2%,相对误差为-22.9%~5.2%,测定结果在证书允许误差范围内。用硅藻土制成高、中、低3个浓度级别的加标回收和精密度实验,加标回收率为84.3%~101.5%,相对标准偏差为0.6%~11.4%,表明方法准确可靠,方法用于实际土壤测定时发现土壤有不同程度的有机氯农药污染。     

EM菌处理垃圾渗滤液的微生物生态学及机理分析研究

通过DNA提取,PCR扩增和DGGE分离,用BLAST程序进行相似性比较分析体系中微生物群落多样性。所有序列与数据库中16S rDNA序列的相似性在94%~100%之间。从整个挂膜过程考虑,挂膜时间应在8天左右。渗滤液中污染物的去除与投加EM有很大的关系,但是渗滤液中原始菌种的贡献同样不可忽视。投加EM菌剂促进了渗滤液中群落结构演替和功能优化,并最终通过EM菌剂和渗滤液中原始菌群的共同作用实现渗滤液处理系统效能提高和完善。     

臭氧+曝气生物滤池深度处理工艺试验研究

针对某污水厂出水不达标的情况,本研究采用臭氧(O3)和曝气生物滤池(BAF)组合工艺对其进行深度处理.结果表明,当采用两级臭氧+曝气生物滤池工艺时,出水COD在31～46 mg/L,色度在13～29倍,均达到一级A排放标准.在最佳运行条件下,臭氧氧化使相对分子质量大于50 000的有机物含量减少10％,小于1 000的有机物含量增加14％.曝气生物滤池工艺使相对分子质量小于1 000的有机物含量降低了24％.     

气相分子吸收光谱法测定氨氮校准曲线斜率、截距参考值研究

主要阐述了气相分子吸收光谱法测定氨氮的校准曲线斜率、截距参考值的分析.文章收集了临安市环境监测站实验室自2012年以来气相分子吸收光谱法氨氮校准曲线制作的一系列原始数据,并通过数理统计方法对校准曲线、残余标准偏差、斜率扩展不确定度、截距扩展不确定度开展了详细讨论,得出气相分子吸收光谱法氨氮校准曲线截距a值、斜率b值实验室参考值.此结果对实验室分析人员判定氨氮项目校准曲线制作是否合格具有一定的参考价值.     

PBDEs的来源特征、环境分布及污染控制

多溴联苯醚(Polybrominated diphenyl ethers,PBDEs)生产应用、环境分布与生态风险之间的关系将如何影响我国的未来,具体涉及到工业、环境、健康、人类繁衍等的社会问题.由于PBDEs阻燃效率高,热稳定性好,价格便宜,作为添加剂被广泛应用在电子、电器、化工、交通、建材、纺织、石油等领域的阻燃产品中.PBDEs进入环境后迁移扩散并富集于沉积物和生物体内,进入人体后引起肝脏毒性、内分泌干扰、神经毒性和生育能力下降等而危害人类的健康.基于此,从生产应用、品种生产量、分子的物理化学特性以及毒性等的文献数据分析了PBDEs的来源特征与环境危害,分析这些性质对环境分布与污染控制的基础支持关系;从沉积物、水体、大气、水生生物、人体5个方面考察了PBDEs的环境本底浓度变化、分配关系、迁移规律、时间效应,分析了生产、应用与扩散的多因素影响关系,发现全球性PBDEs污染物蔓延的现象,沉积物是主要的归趋场所,室内空气中的浓度远高于室外,水中浓度较低,水生生物和人体均能富集PBDEs,通过饮食、母乳和呼吸摄入,可实现代际传播,污染的分布呈现介质与区域的不同特征;污染控制需要考虑点源技术与面源修复的联合,结合PBDEs的物理性质、分子结构及其化学特性,统计分析了微生物法、光化学降解法和零价铁还原法的原理及其有效性,根据PBDEs在产品中存在与分布的特点,提出收集-分离-富集-超临界催化还原和氧化毁毒的工艺,针对实际环境(以电子垃圾塑料和流域水体及沉积物为对象)中的PBDEs进行回收或处理,结合材料如催化剂的应用,从动力学和热力学方面提高PBDEs无害化的效率.最后,从生产管理、环境监测、风险评价、技术集成等方面提出了未来的努力方向.     

植物修复及强化调控系统根际土壤微生物研究综述

根际土壤微生物是植物修复及其强化修复技术的重要组成部分,了解根际土壤微生物生态效应有助于深入探索修复机制,从而进一步提高修复效率.微生物生态效应反映土壤生态变化,对于有效评估强化调控生态风险具有重要意义.在总结污染土壤植物修复根际微生物生态效应研究的基础上,综述强化调控措施与根际土壤微生物可能存在的相互影响,并分析利用微生物分子生态学技术评估强化调控措施施用风险的可行性.     

Remarkable promotion effect of trace sulfation on OMS-2 nanorod catalysts for the catalytic combustion of ethanol

OMS-2 nanorod catalysts were synthesized by a hydrothermal redox reaction method using MnSO₄ (OMS-2-SO₄) and Mn(CH₃COO)₂ (OMS-2-AC) as precursors. SO₄^2 −-doped OMS-2-AC catalysts with different SO₄^2 − concentrations were prepared next by adding (NH₄)₂SO₄ solution into OMS-2-AC samples to investigate the effect of the anion SO₄^2 − on the OMS-2-AC catalyst. All catalysts were then tested for the catalytic oxidation of ethanol. The OMS-2-SO₄ catalyst synthesized demonstrated much better activity than OMS-2-AC. The SO₄^2 − doping greatly influenced the activity of the OMS-2-AC catalyst, with a dramatic promotion of activity for suitable concentration of SO₄^2 − (SO₄/catalyst = 0.5% W/W). The samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectroscopy (ICP-OES), NH₃-TPD and H₂-TPR techniques. The results showed that the presence of a suitable amount of SO₄^2 − species in the OMS-2-AC catalyst could decrease the Mn–O bond strength and also enhance the lattice oxygen and acid site concentrations, which then effectively promoted the catalytic activity of OMS-2-AC toward ethanol oxidation. Thus it was confirmed that the better catalytic performance of OMS-2-SO₄ compared to OMS-2-AC is due to the presence of some residual SO₄^2 − species in OMS-2-SO₄ samples.     

Investigation on the interaction between triclosan and bovine serum albumin by spectroscopic methods

Abstract

Multi-spectroscopic and molecular docking methods were used to study the interaction between triclosan (TCS) and bovine serum albumin (BSA). The results indicated that the fluorescence quenching of BSA by TCS was due to the formation of TCS–BSA complex through static quenching. This result was also demonstrated by time-resolved fluorescence experiment. The binding constants and number of binding sites between TCS and BSA were 1.30?×?10⁵ M^?1 and 1.17 at 298?K, respectively. The thermodynamic parameters were studied in detail which suggested that hydrophobic forces and hydrogen bond played major roles in the TCS–BSA interaction. Moreover, the site marker competitive experiments and docking studies revealed that TCS could bind BSA into site I in subdomain IIA. All the results of UV–vis spectrophotometry, circular dichroism spectroscopy and synchronous fluorescence spectroscopy showed that interaction between TCS and BSA induced conformation changes of BSA.     

Meta-analysis of the differential effects of habitat fragmentation and degradation on plant genetic diversity

Genetic diversity is a key factor for population survival and evolution. However, anthropogenic habitat disturbance can erode it, making populations more prone to extinction. Aiming to assess the global effects of habitat disturbance on plant genetic variation, we conducted a meta-analysis based on 92 case studies obtained from published literature. We compared the effects of habitat fragmentation and degradation on plant allelic richness and gene diversity (equivalent to expected heterozygosity) and tested whether such changes are sensitive to different life-forms, life spans, mating systems, and commonness. Anthropogenic disturbance had a negative effect on allelic richness, but not on gene diversity. Habitat fragmentation had a negative effect on genetic variation, whereas habitat degradation had no effect. When we examined the individual effects in fragmented habitats, allelic richness and gene diversity decreased, but this decrease was strongly dependent on certain plant traits. Specifically, common long-lived trees and self-incompatible species were more susceptible to allelic richness loss. Conversely, gene diversity decreased in common short-lived species (herbs) with self-compatible reproduction. In a wider geographical context, tropical plant communities were more sensitive to allelic richness loss, whereas temperate plant communities were more sensitive to gene diversity loss. Our synthesis showed complex responses to habitat disturbance among plant species. In many cases, the absence of effects could be the result of the time elapsed since the disturbance event or reproductive systems favoring self-pollination, but attention must be paid to those plant species that are more susceptible to losing genetic diversity, and appropriate conservation should be actions taken.     

分子识别作用下光催化降解偶氮染料酸性红GR

合成了β-环糊精(β-CD)与偶氮染料酸性红GR(ARGR)的包结物,并采用红外光谱仪对ARGR、β-CD及β-CD与ARGR的包结物进行了表征,表征结果显示,β-CD与ARGR的包结物的特征峰的峰形和强度与β-CD相似,但峰位有明显的偏移,说明ARGR进入了β-CD空腔与β-CD发生了分子识别作用。采用TiO2作为催化剂,研究了β-CD分子识别后ARGR的光催化降解行为,实验结果表明,在ARGR质量浓度为20.0 mg/L、β-CD浓度为1.8×10-5 mol/L、体系pH为4.0、TiO2加入量为1.0 g/L、光催化反应时间为60 min的条件下,经β-CD分子识别后ARGR的光催化降解率可达100%。