非贵金属催化电解无害化去除硝酸盐氮的反应机制

以Ti/Co-Fe-Cu为阴极,Ti/IrO2-RuO2为阳极组成无隔膜电解体系,对非贵金属催化电解无害化去除NO3--N的反应机制进行了实验研究和理论分析.结果表明,NO3--N阴极催化还原过程中,反应物、产物需要通过对流、扩散作用,克服电场力,迁移至目标位置;在非贵金属的催化作用下,NO3--N受还原剂攻击,逐步还原为NH4+-N;还原中间产物NO-N和NH-N直接生成N2-N的过程受抑制,产物NH4+-N难以被再度直接氧化.添加Cl-作为支持电解质,实验电解体系发生阳极析氯、Cl2水解、NH4+-N氯氧化等过程,可将NH4+-N氧化为N2-N,且出水中NO3--N、NO2--N、氯胺类浓度很低.NO3--N无害化去除的反应机制是NO3--N在催化作用下,经传质、吸脱附、电子交换过程,还原为NH4+-N,NH4+-N经由Cl-→Cl2→HOCl→Cl-电解氯氧化循环,最终生成N2-N.     

洞庭湖湿地Cd富集植物蒌蒿(Artemisia selengensis)的耐性生理机制研究

采用盆栽植株和外源Cd胁迫的方法,分别对不同生长期蒌蒿植株根、叶组织中的抗氧化酶活性、可溶性蛋白及MDA含量进行测定,以揭示蒌蒿在Cd胁迫下的抗氧化机理和耐受机制。研究结果表明,Cd胁迫对上述生理指标均有显著影响:≤20mg·kg-1的Cd处理可使幼苗期植株器官中的可溶性蛋白含量增加16.5%～19.1%,100mg·kg-1的Cd含量水平则导致其含量减少近30%,可溶性蛋白含量的变化与植株的生物量积累关系密切;3种酶活性在0～10mg·kg-1的Cd处理下未显示出明显变化,幼苗期植株CAT、POD活性在10～80mg·kg-1的Cd胁迫下增加明显,高于此浓度范围则使酶蛋白受到破坏而失活,中等含量水平(≤40mg·kg-1)的Cd处理经过长时间作用可使植株逐渐适应胁迫环境,胁迫强度较大的Cd处理可显著提高SOD酶的活性;Cd胁迫过程中植株MDA积累量不断增加。3种抗氧化酶活性的增强在蒌蒿植株耐受Cd胁迫方面能起到较好的防御作用。     

Facilitating sustainable development in Chile: a survey of suitable energy technologies

Sustainable development in developing countries is the main aim of the Kyoto Protocol's Clean Development Mechanism (CDM). However, in the present context, uncertainty prevails as to whether the CDM is actually achieving its aims in terms of achieving sustainable development and to what extent. Chile has several renewable energy and energy efficiency options with significant greenhouse gas (GHG) emissions abatement potential that are not yet financially and economically competitive. In order to be able to identify potential CDM projects and to formulate a series of possible investment strategies with a sustainable development component, it is crucial to establish a clear understanding of the host country's needs and priorities and the suitable sustainable energy technologies to meet these needs. The main scope of this paper is to present results obtained from an elaborated stakeholder assessment on Chile's high priority energy needs and sustainable energy technologies fulfilling these needs in order to assist Chile in finding ways of encouraging technology transfer that would contribute to low-carbon sustainable energy development.     

钛改性锰矿的除砷效果及机理研究

天然锰矿是一种廉价、易得的除砷矿物材料,为了进一步提高天然锰矿的除砷效果和吸附容量,采用TiCl4对广西桂林天然锰矿进行改性,并对其改性的条件进行优化。实验结果表明最佳的改性条件为:TiCl4浓度为10 mg/L,浸泡时间为18 h,pH=3.05,振荡吸附时间为1 h。与天然锰矿的去除效率(82.95%和77.93%)相比,改性锰矿对As(Ⅲ)和As(Ⅴ)去除率分别可达94.87%和99.31%,相应的饱和吸附量分别为3.48 mg/g和3.27 mg/g,较天然锰矿各自提高了1.25 mg/g和1.21 mg/g。改性锰矿对As(Ⅲ)的吸附符合Freundlich等温吸附模型,对As(Ⅴ)的吸附更符合Langmuir等温吸附模型。     

云南高原常见湖滨湿地植物群落对生活污水氮的净化研究

湿地植物具有净化水质的特殊功能,研究不同湿地植物群落对生活污水净化效果及机理,对退化湿地的恢复与人工湿地的构建具有重要的理论和现实意义。选取小黑三棱＋杉叶藻＋荇菜（Com.Sparganium simplex＋Hippuris vulgaris＋Nymphoidespeltatum）、水葱＋睡菜＋荇菜（Com.Scirpus validus＋Menyanthes trifoliate＋Nymphoides peltatum）、菰＋荸荠＋荇菜（Com.Zizaniacaduciflora＋Heleocharis yunnanensis＋Nymphoides peltatum）和香蒲＋睡菜＋眼子菜（Com.Typha przewalskii＋Menyanthestrifoliate＋Potamogeton distinctus）等4种云南高原常见湖滨湿地植物群落作为实验材料进行水质净化模拟研究。结果表明：供试植物都能较好的适应生活污水环境,各植物全株氮质量分数在12.37～19.55 mg.g-1之间,各群落植物氮累积量为229～269 mg.m-2,对生活污水脱氮贡献率为10.11%～11.21%;各群落对生活污水TN的去除率都在75%以上,均显著高于无植物对照组（P〈0.05）,其中水葱＋睡菜＋荇菜（Scirpus validus＋Menyanthes trifoliate＋Nymphoides peltatum）群落对生活污水TN去除效果显著优于其他3种群落（P〈0.05）,去除率高达（93.79±1.27）%;试验期间,各群落污水N03--N与TN浓度之间显著负相关（r=–0.597,P〈0.05）,能很好的揭示氮的去除过程;各群落植物净增生物量与群落TN累积量显著正相关（r=0.953,P〈0.05）,表明收割植物可充分发挥湿地植物的脱氮潜力;植物群落能有效增强和促进湿地系统对污水中氮的净化能力,各植物群落对污水TN去除贡献率在29.24%～43.57%之间,群落内植物生长特性及其种间关系是各植物群落水质净化效果存在显著差异的主要原因。     

金属污染物对神经系统损害及毒性机制研究进展

神经系统与生物体其他系统联系密切,共同维持机体正常的结构和功能。环境中的金属污染物可通过多种途径进入生物体,干扰幼年或成年动物神经系统的发育和功能,其损害机制是目前研究的热点。本文系统地总结了汞、铅和铝等金属污染物对神经系统的损害作用,着重在细胞、分子和基因水平上阐述了金属对神经系统的毒性机制,在此基础上分析了当前研究的不足之处和发展趋势,并对今后的研究方向进行了展望。     

三峡水库香溪河库湾冬季甲藻水华生消机理初探

2010年1—2月在香溪河库湾上、中、下游各选取1个监测点对水体环境因子及藻类进行监测,对水温、营养盐含量等进行分析,探讨香溪河库湾冬季甲藻水华的生消机理. 结果表明:2010年冬季,香溪河库湾末端暴发了甲藻水华,持续44 d,优势藻种为拟多甲藻(Peridiniopsis sp.),最高细胞密度达到11.8×106 L-1;适宜的水温、充足的营养盐以及良好的光照、弱分层水体是香溪河库湾冬季甲藻水华暴发的主要原因;Zmix/Zeu〔Zmix(混合层深度)与Zeu(真光层深度)之比〕在2~3之间时有利于甲藻生长;库湾中下游因水体掺混强烈而在冬季未暴发水华;后期水体分层状态的加强及Zmix/Zeu的减小是甲藻水华消失的主要原因.      

声电氧化处理亚甲基蓝废水的研究

采用电沉积法制备了稀土和氟树脂等共掺杂的新型二氧化铅电极,并用于声电氧化体系中作为阳极处理典型模拟染料废水.考察了声电耦合氧化条件下的协同因子变化,发现PbO2/Ti电极和La-PbO2/Ti电极作阳极时,协同因子分别为1.29、1.36.考察并优化了该氧化镧掺杂电极用于声电氧化体系的作用因素,结果表明,在功率为49.58W/cm2、频率为50Hz、阳极电极为La-PbO2/Ti电极、电流密度为71.43mA/cm2、硫酸钠为14.2g/L的条件下,200mg/L的亚甲基蓝模拟废水经过2h后去除率达到89.51%.通过GC-MS、IC等分析手段检测了中间产物,提出了亚甲基蓝可能的降解途径.     

The interaction of heat shock proteins and some components of plant viruses北大核心CSCD

Considerable research has indicated that heat shock proteins (Hsp), as molecular chaperones, carry out many biological activities of plant viruses by folding, transporting, translocating, assembling, or degrading client proteins. It is fundamental to develop resistant plant varieties and novel anti-viral agents by determining the interaction mechanisms between plant viruses and hosts. In this study, we first reviewed the classification, gene and protein structure, and biological significances. We then analyzed the assembling mechanism of Hsp70 or Hsp90, plant host cofactors, and RNA-dependent RNA polymerases in a viral replicase complex, and the mechanism of interaction and subcellular localization between Hsp70 and some plant virus components. We highlighted the mechanism of interaction and movement between Hsp70 and some plant virus components and the effect of Hsp expression of plant hosts or viruses. The results indicated where the mechanism occurred, the participating factors, energy supply, and material conversion between Hsps and the plant virus components for the course of the intracellular movement, local movement between cells, and long-distance movement, and showed the Hsp type specificity and the law of dynamic Hsp expression in plant hosts infected by viruses. The studies mainly focused on the two Hsp factors and the plant viral components, indicating limited coordination mechanisms among many nucleic acids, proteins, and polysaccharides in macromolecular protein complexes (MRC). Future research should analyze the translocation mechanism between client proteins and Hsps, the coordination mechanism between Hsps and MRC components, and the relation between MRC and the plant tissue structure. © 2018 Science Press. All rights reserved.     

Application and mechanism of polysaccharide extracted from Enteromorpha to remove nano-ZnO and humic acid in coagulation process

Green source Ep was extracted from marine alga waste. The molecule model structure of Ep was studied and constructed. PAC-Ep coagulation system improves the efficiency of removal efficiency. Synergistic effects between NPs and HA make a big difference to enhance efficiency. Mechanism is charge neutralization, hydrogen bonding and adsorbing-complexing Enteromorpha polysaccharide (Ep) extracted from alga a novel green coagulant aid for nanoparticles (NPs) and heavy metal ions removal and the structure of EP was intensively studied in this study. The integration of Ep with polyaluminum chloride (PAC-Ep) coagulants exhibited higher coagulation performance than that of the polyaluminum chloride (PAC) because of the negatively charged NPs suspension and humic aid (HA) solution. Significant high removal efficiencies of dissolved organic matter (94.1%), turbidity (99.3%) and Zn ions (69.3%) were achieved by the PAC-Ep coagulants. The dual-coagulation properties of PAC-Ep for different pollutants was based on multiple mechanisms, including (i) Al³⁺ charge neutralization; (ii) hydroxy aluminum hydroxyl bridging formed polynuclearhydroxy complexes bridge and sweep colloidal particles; (iii) adsorption and bridging of Ep chain for the NPs and heavy metal ions. Results indicated that the destabilization of colloid was induced by the coexisting HA and higher removal was achieved as ions adsorption was enhance in the presence of HA complexation. On the basis of that, the extraction of polysaccharide is a promising candidate for its high coagulation performance in water treatment.