青藏高原东北部地区表层土壤中全氟化合物的分布特征及来源解析

为探讨全氟化合物（PFASs）在偏远地区的赋存水平及其来源,采用超高效液相色谱-串联质谱法分析了青藏高原东北部地区18个点位表层土壤中12种PFASs含量水平和分布特征,并对其进行来源解析.结果表明,土壤中有11种PFASs检出,■范围为0.043～1.573 ng·g^-1,平均值为0.398 ng·g^-1,其中单体PFBA的含量最高(平均值为0.164 ng·g^-1),PFHxA含量最低(平均值为0.005 ng·g^-1),其他单体PFASs含量处于同一水平(平均值为0.011～0.057 ng·g^-1),短链PFASs是该区域PFASs的主要贡献者. PFASs空间分布整体表现为西和北部较高,东南较低,PFBA存在高山冷凝效应.主成分分析表明,青藏高原东北部区域土壤中PFASs主要来源于PFASs及其前体物大气传输至此发生的沉降和降解,少数地区受点源污染直接排放影响,金属和矿产等工业生产和人类活动是其主要来源.     

地膜覆盖对农田土壤养分和生态酶计量学特征的影响

生态酶计量比可以用来衡量土壤微生物能量和养分资源限制状况.为明确地膜覆盖后农田土壤生态酶计量学特征,选取地膜覆盖下不同残膜积累量的农田土壤,利用荧光分析法测定其碳氮磷循环关键过程中的β-1,4-葡萄糖苷酶（BG）、β-1,4-N-乙酰氨基葡萄糖苷酶（NAG）和磷酸酶（ACP）的活性.探讨地膜覆盖对农田土壤养分循环和供应的影响.结果表明,施用化肥的土壤,覆膜使Olsen-P和NO^-₃-N分别降低至不覆膜土壤的48%～62%和16%～24%;而有机-无机配施的土壤,两者在覆膜条件下分别提高了144%～203%和1.9～5.1倍.覆膜下SOC∶TN在有机-无机配施土壤中降低了6.6%～25.8%,而SOC∶TP和TN∶TP却显著增加.覆膜土壤中MBC含量均显著低于不覆膜的土壤,然而由于MBN和MBP也随之降低,MBC∶MBN和MBC∶MBP无显著差异;覆膜使MBN∶MBP在S1和S2分别降低了36.6%和23.8%,而在S3和S4中分别提高了5.4和1.3倍.土壤中NAG∶ACP计量比与微生物生物量中相对应的元素的计量比趋势相似;而覆膜下BG∶NA...     

咪唑银配位聚合物吸附偶氮染料研究

以咪唑银配位聚合物{Ag（im）}n作吸附剂,对偶氮染料刚果红和甲基橙的吸附进行了研究,结果表明：刚果红的最佳吸附条件是吸附剂加入量为31．5mg,温度为30℃,pH值为3,吸附时间为70min,最高染料脱除率为90。7％;甲基橙的最佳吸附条件是吸附剂加入量为36．7mg,温度为30℃,pH值为2,吸附时间为50min,最高染料脱除率为58．3％。     

Sustainable monitoring of concrete structures: strength and durability performance of polymer-modified self-sensing concrete

Concrete structures all over the world are reaching the end of their service life sooner than expected. This is due to the fact that ordinary Portland cement-based concrete deteriorates under environmental actions and also that structural inspections and conservation actions are expensive. Besides, as they consume energy and non-renewable resources, they have negative environmental impacts. Self-sensing concrete provides an alternative way of monitoring concrete-reinforced structures at a much lesser cost and with lesser environmental impact. Although the short-term mechanical properties of these materials are usually well documented, the long-term durability issues about carbon fibre concrete still deserve further investigations. This paper reports some investigation of the strength and durability characteristics of several concrete mixtures modified with different percentages of polymer and carbon fibre addition. The results show that the addition of carbon fibre decreases the strength and increases water penetration under pressure and also increases chloride diffusion, whereas polymer addition is responsible for a denser microstructure and higher concrete durability.     

电化学脱稳技术处理油田含聚污水

采用"电化学除油器—斜板除油器—核桃壳过滤器"模拟装置处理模拟含聚采油污水,考察了有/无清水剂加入条件下含聚污水的处理效果,并对电化学除油机理进行了分析。实验结果表明:各级处理单元的除油率与电化学处理时间成正比,不加入清水剂、电化学处理40 min时,各级处理单元的除油率均超过92%;在电化学除油器前加入清水剂100 mg/L、电化学处理20 min时,各级处理单元的除油率分别为98.8%~99.4%,处理后污水含油量小于30 mg/L,处理效果优于在斜板除油器前加入清水剂;电化学处理与清水剂处理有良好的协同除油效果,可大幅降低清水剂用量。机理分析结果表明,电化学作用主要使吸附于油-水界面的产出聚合物降解、脱稳,实现了对油-水界面膜强度和界面电荷的有效破坏,除油效果优异且处理后的絮体松散、无黏附性。     

双亲型清水剂处理油田含聚污水

考察了双亲型清水剂QS-03对油田含聚污水处理效果的影响因素,并对其作用机理进行了分析。实验结果表明:当清水剂QS-03的亲水性与亲油性功能基团的摩尔比为2∶1、清水剂加入量大于等于200 mg/L时,处理后污水澄清透明,污水含油量由4 540 mg/L大幅降至26~45 mg/L;在处理温度为50~80℃和污水含油量为3 200~5 800 mg/L的范围内,清水剂QS-03均表现出良好的清水效果,生成的絮体呈松散状,具有良好的流动性。机理分析结果表明,双亲型清水剂QS-03可有效破坏油-水界面双电层、降低界面膜强度,并且与污水中阴离子聚合物的相互作用大幅减弱,因而在高效清水除油的同时可有效避免含聚污水处理中的黏性"含聚油泥"问题。     

Biosorption of Cu(Ⅱ) on extracellular polymers from Bacillus sp.F19

Biosorption can be an effective process for the removal of heavy metals from aqueous solutions.The adsorption of Cu(Ⅱ) from aqueous solution on the extracellular polymers (EPS) from Bacillus sp.(named MBFF19) with respect to pH,incubation time,concentration of initial Cu(Ⅱ),and biosorbent dose was studied.Biosorption of Cu(Ⅱ) is highly pH dependent.The maximum uptake of Cu(Ⅱ) (89.62 mg/g) was obtained at pH 4.8.Biosorption equilibrium was established in approximately 10 min.The correlation coeffcient of mor...     

膜分离腐殖质前后晚期渗滤液可生化性的变化

晚期渗滤液由于含有大量难降解有机物腐殖质,可生化性差,较难处理。采用特定分子量的超滤膜对晚期渗滤液中的腐殖质进行有效的分离,研究了膜分离腐殖质前后渗滤液的可生化性的变化：渗滤液中腐殖质类物质去除率为90．7％,BOD5/COD值提高了6倍,可生物降解的有机物在总有机物中所占比率提高了约4倍。结果表明,分离腐殖质可提高渗滤液的可生化性。     

Interaction and combined toxicity of microplastics and per- and polyfluoroalkyl substances in aquatic environment

● Adsorption of PFASs on MPs and its mechanisms are critically reviewed. ● MPs could alter the transport and transformation of PFASs in aquatic environments. ● Combined toxicity of MPs and PFASs at organismal and molecular levels is discussed. Microplastics (MPs) are recognized as vectors for the transport of organic contaminants in aquatic environments in addition to their own adverse effects on aquatic organisms. Per- and polyfluoroalkyl substances (PFASs) are widely present in aquatic environments due to their widespread applications, and thus coexist with MPs. Therefore, we focus on the interaction of MPs and PFASs and related combined toxicity in aquatic environments in this work. The adsorption of PFASs on MPs is critically reviewed, and new mechanisms such as halogen bonding, π-π interaction, cation-π interactions, and micelle formation are proposed. Moreover, the effect of MPs on the transport and transformation of PFASs in aquatic environments is discussed. Based on four typical aquatic organisms (shellfish, Daphnia, algae, and fish), the toxicity of MPs and/or PFASs at the organismal or molecular levels is also evaluated and summarized. Finally, challenges and research perspectives are proposed, and the roles of the shapes and aging process of MPs on PFAS biogeochemical processes and toxicity, especially on PFAS substitutes, are recommended for further investigation. This review provides a better understanding of the interactions and toxic effects of coexisting MPs and PFASs in aquatic environments.     

沱江流域典型及新兴全氟/多氟化合物的污染特征及来源解析

为研究沱江流域表层水中全氟/多氟化合物（PFASs）的污染特征和来源,采用超高效液相色谱-串联质谱（UPLC-MS/MS）分析了沱江48个表层水样中的PFASs.结果表明,沱江流域水体中ρ（ΣPFASs）为12.5~3789 ng·L^-1,其中全氟辛烷羧酸（PFOA）为最主要污染组分,ρ（PFOA）为9.97~3764 ng·L^-1,占比高达73.6%~99.8%,说明传统PFASs仍是沱江流域主要的PFASs.所涉新兴PFASs检出率最高的为F-53B,检出率达100%,F-53B已在沱江流域被广泛使用.沱江流域浓度最高的新兴PFASs为6：2氟调聚磺酸（6：2 FTS）［nd~27.3 ng·L^-1,平均值为（9.12±7.70） ng·L^-1］,与国内外其它河流相比,处于较高污染水平.工业园区附近采样点的PFASs污染水平较高,其次为沱江下游的泸州河段,说明氟工业园区排放和人类日常生产活动是造成沱江流域PFASs污染的主要影响因素.最后,通过估算得出,沱江流域水相向长江排放的PFASs通量为353 kg·a^-1,其中排放通量最高组分为PFOA （348 kg·a^-1）,可为沱江流域PFASs管控提供基础数据.