离子液体吸收废印刷线路板热拆解过程中挥发性有机物——基于COSMO-RS模型

模拟废印刷线路板（WPCB）的热拆解过程,分析热拆解过程中的挥发性有机物（VOCs）组分;利用真实溶剂似导体屏蔽（COSMO-RS）模型对浓度较高的污染物进行量子力学模拟,研究离子液体（ILs）组成单元对目标污染物溶解度的影响差异,分析溶解过程中主导分子间作用力类型,确定优选吸收剂;测定不同溶剂进行溶解性,验证模型适用性.结果表明：①乙酸乙酯和环戊酮是浓度较高的VOCs组分,在240和250℃时浓度分别为43.1,153mg/m³和105,252mg/m³,质量百分比总和分别为76.3%和67.3%.②高表面屏蔽电荷密度分布峰、长烷基链阴阳离子和亲电基团的存在可提高乙酸乙酯和环戊酮在ILs中的溶解度.双三氟甲磺酰基亚胺盐（NTf₂^-）类ILs是一类优良吸收剂.静电力和范德华力对溶解过程起主导作用.③COSMO-RS模型可定性和半定量用于预测乙酸乙酯和环戊酮的溶解度.     

Quantitative structure-property relationship of aromatic sulfur-containing carboxylates

IntroductionItiswidelyrecognizedthatthephysicochemicalprofileoforganicchemicalslargelydeterminestheirdistributionbetweenenvironmentalmedia .Fortheenvironmentalbehaviorsoforganiccontaminants,watersolubility(SW)andoctanol waterpartitioncoefficient(KOW)aretremendouslyimportant.Octanol waterpartitioncoefficienthasbeenwidelyrelatedtobiochemicaland orbiologicalactivityinquantitativestructure activityrelationships(QSARs) (Leo ,1 971 ) .Watersolubilitycorrespondstothedispersiontendencyandtothereca…     

Effect of long-term fertilization on soil nitrate distribution

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Reservoir‐host amplification of disease impact in an endangered amphibian

Emerging wildlife pathogens are an increasing threat to biodiversity. One of the most serious wildlife diseases is chytridiomycosis, caused by the fungal pathogen, Batrachochytrium dendrobatidis (Bd), which has been documented in over 500 amphibian species. Amphibians vary greatly in their susceptibility to Bd; some species tolerate infection, whereas others experience rapid mortality. Reservoir hosts—species that carry infection while maintaining high abundance but are rarely killed by disease—can increase extinction risk in highly susceptible, sympatric species. However, whether reservoir hosts amplify Bd in declining amphibian species has not been examined. We investigated the role of reservoir hosts in the decline of the threatened northern corroboree frog (Pseudophryne pengilleyi) in an amphibian community in southeastern Australia. In the laboratory, we characterized the response of a potential reservoir host, the (nondeclining) common eastern froglet (Crinia signifera), to Bd infection. In the field, we conducted frog abundance surveys and Bd sampling for both P. pengilleyi and C. signifera. We built multinomial logistic regression models to test whether Crinia signifera and environmental factors were associated with P. pengilleyi decline. C. signifera was a reservoir host for Bd. In the laboratory, many individuals maintained intense infections (>1000 zoospore equivalents) over 12 weeks without mortality, and 79% of individuals sampled in the wild also carried infections. The presence of C. signifera at a site was strongly associated with increased Bd prevalence in sympatric P. pengilleyi. Consistent with disease amplification by a reservoir host, P. pengilleyi declined at sites with high C. signifera abundance. Our results suggest that when reservoir hosts are present, population declines of susceptible species may continue long after the initial emergence of Bd, highlighting an urgent need to assess extinction risk in remnant populations of other declined amphibian species.     

干热河谷林地燥红土固碳特征及"新固定"碳表观稳定性

全球气候变化背景下,森林土壤固碳能力及所固定碳的稳定性受到极大关注.基于土壤密度分组和酸水解技术,对比研究了1991年营造的大叶相思(Acacia auriculiformis)林不同阶段(1991、1997、2003和2010年)土壤及其物理和生化组分中有机碳密度.结果表明,造林19 a后林地表层(0～15 cm)和亚表层(15～30 cm)土壤有机碳密度分别为1.40 kg.m-2和0.99kg.m-2.研究期内(1991～2010年)表层和亚表层土壤平均固碳速率分别为37.89 g.(m2.a)-1和16.84 g.(m2.a)-1,且土壤呈现加速固碳特征.2003年林地表层重组有机碳分配比例为71.44%,显著高于2010年(67.99%).2003年林地表层或亚表层轻组顽固性碳指数显著高于重组,但均随林龄的增加而降低,尤其是轻组顽固性碳指数.2003～2010年间燥红土"新固定"碳中57%～70%受物理保护,33%～49%为生化稳定性碳.研究揭示出干热河谷人工林燥红土具备较大的固碳能力.受物理保护碳的生化稳定性低于非保护碳,其稳定性均随林龄的增加而降低.     

Kinetics of selective catalytic reduction of NO by NH3 on Fe-Mo/ZSM-5 catalyst

The catalyst of Fe-Mo/ZSM-5 has been found to be more active than Fe-ZSM-5 and Mo/ZSM-5 separately for selective catalytic reduction (SCR) of nitric oxide (NO) with NH3. The kinetics of the SCR reaction in the presence of O2 was studied in this work. The results show that the observed reaction orders were 0.74-0.99, 0.01-0.13, and 0 for NO, O2 and NH3, respectively, at 350-450℃. And the apparent activation energy of the SCR was 65 kJ/mol on the Fe-Mo/ZSM-5 catalyst. The SCR mechanism was also deduced. Adsorbed NO species can react directly with adsorbed ammonia species on the active sites to form N2 and H2O. Gaseous O2 might serve as a reoxidizing agent for the active sites that have undergone reduction in the SCR process. It is also important to note that a certain amount of NO was decomposed directly over the Fe-Mo/ZSM-5 catalyst in the absence of NH3.     

Reversibly enhanced aqueous solubilization of volatile organic compounds using a redox-reversible surfactant

Surfactant-enhanced remediation (SER) is an effective method for the removal of volatile organic compounds (VOCs) from contaminated soils and groundwater. To reuse the surfactant the VOCs must be separated from the surfactant solutions. The water solubility of VOCs can be enhanced using reversible surfactants with a redox-acive group, (ferrocenylmethyl)dodecyldimethylammonium bromide (Fcl2) and (ferrocenylmethyl)tetradecanedimethylammonium bromide (Fcl4), above and below their critical micelle concentrations (CMC) under reducing (I⁺) and oxidative (I²⁺) conditions. The CMC values of Fcl2 and Fcl4 in I⁺ are 0.94 and 0.56 mmol/L and the solubilization of toluene by Fcl2 and Fcl4 in I⁺ for toluene is higher than the solubilization achieved with sodium dodecyl sulfate, cetyltrimethylammonium bromide and Trition X-114. The solubilization capacity of the ferrocenyl surfactants for each tested VOCs ranked as follows: ethylbenzene > toluene > benzene. The solubilities of VOCs by reversible surfactant in I⁺ were 30% higher than those in I²⁺ at comparable surfactant concentrations. The effects of Fcl4 concentrations on VOCs removal efficiency were as follows: benzene > toluene > ethylbenzene. However, an improved removal efficiency was achieved at low ferrocenyl surfactant concentrations. Furthermore, the reversible surfactant could be recycled through chemical approaches to remove organic pollutants, which could significantly reduce the operating costs of SER technology.     

表面活性剂Burkholderia xenoborans LB400体系对低氯代PCBs的好氧强化降解

增强多氯联苯(PCBs)的水溶性是强化PCBs微生物降解的主要控制因素之一,本研究选取了PCB5(2,3-CB)和PCB31(2,4',5-CB)作为低氯代PCBs的典型代表,以曲拉通100(TX-100)、吐温80(Tween 80)、鼠李糖脂粗提物(RL crude)3种表面活性剂和β-环糊精( HPCD)联合Burkholderia xenoνorans LB400构建PCBs好氧降解体系,测试了它们对PCB5和PCB31的溶出率及微生物生长的影响.结果表明,TX-100(CMC＝194 mg·L-1)、 Tween 80(CMC＝13.1 mg·L-1)、 RL crude(CMC＝50 mg·L-1)浓度在1~7 CMC 时和 HPCD 浓度在500~1500 mg·L-1时对 PCB5和 PCB31溶出率分别达到54.7％~100％、59.8％~100％;10.5％~40.8％、6.8％~31.6％;10.3％~19.9％、3.3％~11.6％和19.5％~34.2％、4.2％~10.7％. TX-100浓度在1~7 CMC时对B. xenoνorans LB400生长的抑制率达到30.3％~45.8％,而Tween 80浓度在0.1~1 CMC时对其生长的抑制率为10.0％~15.4％; RL crude 本身能作为底物促进 LB400的生长,而 HPCD 对其生长无明显影响. B. xenoνorans LB400对PCB31(5 mg·L-1)的降解效率在添加表面活性剂后有不同程度的提高：TX-100,23.7％~65.5％; Tween 80,14.6％~44.3％;RL crude,9.6％~27.2％;HPCD,15.3％~20.7％;而表面活性剂对PCB5(10 mg·L-1)的降解效率则无明显影响.表面活性剂主要通过增大溶液中PCBs-表面活性剂的胶束浓度来提高LB400对PCBs的降解效率,在水溶液培养体系中当设置TX-100和Tween 80浓度分别在1和7 CMC时,PCB31的降解效率达到100％和81.7％,而此时B. xenoνorans LB400生长的抑制率为30.3％和5.4％.     

北京大气颗粒物和重金属铅干沉降通量及季节变化

为了解大气颗粒物和重金属铅(Pb)干沉降通量的变化规律,采用聚氨酯泡沫膜片为代用面联合干湿沉降自动观测设备,于2013年12月~2014年11月在北京城区采集了颗粒物干沉降,利用微波消解和电感耦合等离子体质谱仪对样品中全量Pb和水溶性Pb进行了测试分析.结果表明,北京大气颗粒物和Pb干沉降通量分别为0.84 t·(hm~2·a)~(-1)和7.56mg·(m~2·a)~(-1),呈现出春季冬季秋季~夏季的特征.大气颗粒物中水溶性Pb干沉降通量为3.14 mg·(m~2·a)~(-1),占Pb干沉降总量的43%,这一比例呈现出冬春季高于夏秋季的特征.人为源排放不仅增加了大气颗粒物和Pb的干沉降通量,也改变了水溶性Pb干沉降通量的季节分布.研究结果对科学评估重金属沉降的生态影响和健康效应提供了科学基础,同时凸显了消减人为源重金属排放的重要性.