裂解温度和离子强度对不同来源生物炭胶体释放行为的影响

近年来环境中生物炭胶体形成受到广泛关注,它是生物炭在环境中物理分解作用的重要过程,对污染物迁移有着重要影响.然而,目前对生物炭胶体释放过程和影响因素的研究甚少,人们对生物炭胶体释放机理的认识还很有限.本研究以小麦秸秆和花生壳为生物质来源,系统地探讨了生物炭的裂解温度（300~700 ℃）和溶液离子强度（0.1~10 mmol·L^-1）对生物炭胶体产率的影响.结果表明,随着裂解温度的升高,生物炭的耐磨性增强,且在较高的裂解温度下（≥500 ℃）花生壳生物炭的耐磨性显著强于小麦秸秆生物炭.生物炭的胶体产率受到生物质来源和裂解温度的显著影响,花生壳生物炭的胶体产率低于小麦秸秆生物炭,高温裂解（≥600 ℃）生物炭的胶体产率显著低于中低温裂解生物炭.在相同溶液离子强度下,生物炭胶体产率与其亚微米级碎片率呈显著正相关（p<0.05）,即生物炭中亚微米级碎片率越高,生物炭胶体产率越高.当溶液离子强度从1 mmol·L^-1增加到10 mmol·L^-1时,两种来源生物炭的胶体产率均显著降低,其降低的程度因生物炭裂解温度而异,其中低温裂解（300 ℃）生物炭的胶体产率降低了11.1%~11.2%,中高温裂解（≥ 500 ℃）生物炭的胶体产率降低了60.0%~97.2%.     

Effect of humic acids on physicochemical property and Cd(II) sorption of multiwalled carbon nanotubes

Zinc pyrithione is used as an antifouling agent. However, the environmental impacts of zinc pyrithione have recently been of concern. Zinc induces diverse actions during oxidative stress; therefore, we examined the effect of zinc pyrithione on rat thymocytes suffering from oxidative stress using appropriate fluorescent probes. The cytotoxicity of zinc pyrithione was not observed when the cells were incubated with 3 μM zinc pyrithione for 3 h. However, zinc pyrithione at nanomolar concentrations (10 nM or more) significantly increased the lethality of cells suffering from oxidative stress induced by 3 mM H₂O₂. The application of zinc pyrithione alone at nanomolar concentrations increased intracellular Zn²⁺ level and the cellular content of superoxide anions, and decreased the cellular content of nonprotein thiols. The simultaneous application of nanomolar zinc pyrithione and micromolar H₂O₂ synergistically increased the intracellular Zn²⁺ level. Therefore, zinc pyrithione at nanomolar concentrations may exert severe cytotoxic action on cells simultaneously exposed to chemicals that induce oxidative stress. If so, zinc pyrithione leaked from antifouling materials into surrounding environments would be a risk factor for aquatic ecosystems. Alternatively, zinc pyrithione under conditions of oxidative stress may become more potent antifouling ingredient.     

南太湖沉积物磷的释放研究

南太湖沉积物磷的释放与沉积物有机质含量、上覆水的化学性质、沉积物－水系统的细菌总数及湖泊水动力对沉积物释磷影响最强烈、沉积物因有机物含量不同，导致总有机磷、总氮、有机硫、水溶性无机硫含量差异，明显影响着磷的释放。沉积物－水系统的细菌总数与沉积物的释磷量存在显著性相关，而某细菌数量与释磷量相关笥不显著。对有机质含量低的沉积物，上覆水的ＢＯＤ，ＮＨ２－Ｎ浓度越高，磷的释放量越大。     

水库网箱养鱼环境经济学分析

以密云水库为研究对象，分析了水库网箱养鱼对水库局部水域水质和水库出水水质的影响程度，并从环境经济学角度对水库网箱养鱼进行了费用－效益分析，指出应禁止在密云水库进行网箱养鱼作业。     

Fate and transport of engineered nanomaterials in the environment

With the fast development of nanotechnology, engineered nanomaterials (ENMs) will inevitably be introduced into the various environment. Increasing studies showed the toxiccity of various ENMs, which raises concerns over their fate and transport in the environment. This review focuses on advances in the research on environmental transport and fate of ENMs. Aggregation and suspension behaviors of ENMs determining their fate and transport in aqueous environment are discussed, with emphasis on the influencing factors, including natural colloids, natural organic matter, pH, and ionic strength. Studies on the transport of ENMs in porous media and its influencing factors are reviewed, and transformation and organismcleansing, as two fate routes of ENMs in the environment, are addressed. Future research directions and outlook in the environmental transport and fate of ENMs are also presented.     

Sorption mechanism of naphthalene by diesel soot: Insight from displacement with phenanthrene/p-nitrophenol

The nonlinear sorption of hydrophobic organic contaminants (HOCs) could be changed to linear sorption by the suppression of coexisting solutes in natural system, resulting in the enhancement of mobility, bioavailability and risks of HOCs in the environment. In previous study, inspired from the competitive adsorption on activated carbon (AC), the displaceable fraction of HOCs sorption to soot by competitor was attributed to the adsorption on elemental carbon fraction of soot (EC-Soot), while the linear and nondisplaceable fraction was attributed to the partition in authigenic organic matter of soot (OM-Soot). In this study, however, we observed that the linear and nondisplaceable fraction of HOC (naphthalene) to a diesel soot (D-Soot) by competitor (phenanthrene or p-nitrophenol) should be attributed to not only the linear partition in OM-Soot, but also the residual linear adsorption on EC-Soot. We also observed that the competition on the surface of soot dominated by external surface was different from that of AC dominated by micropore surface, i.e., complete displacement of HOCs by p-nitrophenol could occur for the micropore surface of AC, but not for the external surface of soot. These observations were obtained through the separation of EC-Soot and OM-Soot from D-Soot with organic-solvent extraction and the sorption comparisons of D-Soot with an AC (ACF300) and a multiwalled carbon nanotube (MWCNT30). The obtained results would give new insights to the sorption mechanisms of HOCs by soot and help to assess their environmental risks.     

Removal of dispersant-stabilized carbon nanotubes by regular coagulants

Coagulation followed by sedimentation, as a conventional technique in the water treatment plant, can be the first line of defense against exposures of carbon nanotubes (CNTs) to aquatic organisms and human beings, which has been rarely documented. This study investigated the removal of dispersant-stabilized CNT suspensions by poly aluminum chloride (PACl) and KAl(SO₄)₂. 12H₂O (alum), with a focus on the effects of dispersant type, coagulant type and dosage. PACl performed better than alum in the removal of tannic acid-, humic acid-, and sodium dodecyl benzenesulfonate-stabilized CNTs, but worse for polyethylene glycol octylphenyl ether (TX100)-stabilized CNTs. Neither coagulant could effectively precipitate cetyltrimethyl ammonium bromide-stabilized CNTs. The removal by PACl first increased up to a plateau and then decreased with the continued increase of coagulant dosage. However, the removal rates leveled off but did not decrease after achieving their highest level with the continued addition of alum. The coagulation and flocculation of the CNT suspensions by PACl could be regulated mainly by the mechanism of adsorption charge neutralization, whereas the coagulation by alum mainly involved electrical double-layer compression.     

Release and sedimentation behaviors of biochar colloids in soil solutions

The release of biochar colloids considerably affects the stability of biochar in environment. Currently, information on the release behavior and suspension stability of biochar colloids in real soil solutions is scarce. In this study, 20 soils were collected from different districts in China and the release behavior of biochar colloids and their suspension stability in soil solutions were systematically examined. The results showed that both pyrolysis temperature and biomass source had important effects on the formation of biochar colloids in soil solutions. The formation amount of biochar colloids from low pyrolysis temperatures (400 °C) (average amount of 9.33–16.41 mg/g) were significantly higher than those from high pyrolysis temperatures (700 °C) (average amount of less than 2 mg/g). The formation amount of wheat straw-derived biochar colloids were higher than those of rice straw-derived biochar colloids probably due to the higher O/C ratio in wheat-straw biochar. Further, biochar colloidal formation amount was negatively correlated with comprehensive effect of dissolved organic carbon, Fe and Al in soil solutions. The sedimentation curve of biochar colloids in soil solutions is well described by an exponential model and demonstrated high suspension stability. Around 40% of the biochar colloids were maintained in the suspension at the final sedimentation equilibrium. The settling efficiency of biochar colloids was positively correlated with comprehensive effect of the ionic strength and K, Ca, Na, and Mg contents in soil solutions. Our findings help promote a deeper understanding of biochar loss and stability in the soil-water environment.     

Interactions of extracellular DNA with aromatized biochar and protection against degradation by DNase I

With increasing environmental application, biochar (BC) will inevitably interact with and impact environmental behaviors of widely distributed extracellular DNA (eDNA), which however still remains to be studied. Herein, the adsorption/desorption and the degradation by nucleases of eDNA on three aromatized BCs pyrolyzed at 700 °C were firstly investigated. The results show that the eDNA was irreversibly adsorbed by aromatized BCs and the pseudo-second-order and Freundlich models accurately described the adsorption process. Increasing solution ionic strength or decreasing pH below 5.0 significantly increased the eDNA adsorption on BCs. However, increasing pH from 5.0 to 10.0 faintly decreased eDNA adsorption. Electrostatic interaction, Ca ion bridge interaction, and π-π interaction between eDNA and BC could dominate the eDNA adsorption, while ligand exchange and hydrophobic interactions were minor contributors. The presence of BCs provided a certain protection to eDNA against degradation by DNase I. BC-bound eDNA could be partly degraded by nuclease, while BC-bound nuclease completely lost its degradability. These findings are of fundamental significance for the potential application of biochar in eDNA dissemination management and evaluating the environmental fate of eDNA.     

人工纳米材料对贝类生态毒理效应的研究进展

纳米技术已成为21世纪发展最迅猛的技术领域之一。纳米材料因其具备新异的物理、化学特性而广泛应用于各种领域,包括农业,电子工业,生物医学,制造业,医药品和化妆品等,因此纳米颗粒不可避免会释放到水环境中。贝类由于其具有分布广,处于食物链中的关键位置,滤食食性,对重金属及污染物有较强的生物累积能力,且很多贝类具有养殖和商业价值,因而纳米颗粒对贝类的生态毒性效应备受关注。本文通过对已有相关研究成果进行归纳分析,重点阐述了3方面的内容:1)人工纳米材料在水环境中的行为;2)贝类作为水生污染监测指示生物的重要意义;3)人工纳米材料对贝类的毒性效应,主要包括贝类对纳米颗粒摄取、积累和转移,并从组织细胞水平,分子和基因水平,胚胎发育和个体生长水平等阐述了纳米材料对贝类的毒性效应。