重庆三峡库区非点源污染评价与影响因子分析

选取重庆三峡库区4个行政建制镇进行非点源污染监测与调查,以COD、TN、TP、Cu、Zn等指标为主要研究内容对库区农村环境进行污染特性分析并且利用等标污染负荷法对其生活污水、生活垃圾、畜禽养殖、水产养殖、化肥流失、农药流失、水土流失等污染源进行非点源污染评价。结果表明:COD、TN、TP、Cu、Zn的平均排放浓度分别为22.15 mg/L、6.37 mg/L、1.49 mg/L、47.73 g/kg、85.24 g/kg,库区主要污染物依次为TN、TP、COD、Cu、Zn等,主要污染源依次是畜禽养殖、化肥流失、生活污水、生活垃圾、农药流失、水土流失、水产养殖等。采用SPSS软件对影响库区环境污染的季节、收入水平、地域、畜禽养殖规模、环境基础设施完善程度等因子进行了分析,结果显示:COD主要影响因子是地域和畜禽养殖规模,TN主要影响因子是季节、地域和畜禽养殖规模,TP主要影响因子是环境基础设施完善程度、畜禽养殖规模和地域,Cu、Zn主要影响因子均是畜禽养殖规模。该研究可为重庆三峡库区生态修复、城乡统筹下的城乡规划及产业布局提供理论基础。     

絮凝剂聚硅酸锌铁(PZFSiC)的研制和性能

在高模数水玻璃溶液中加入酸制备出聚硅酸,再引入适量的金属离子M(Zn、Fe),研制出一种新型的无毒无机复合高分子絮凝剂聚硅酸锌铁(PZFSiC).探讨了M与SiO2不同浓度比和不同pH值对PZFSiC的絮凝效果的影响,通过正交实验找出了最佳的制备工艺条件.在此基础上,进一步对两种不同的水样进行了絮凝实验,确定出水处理中最佳絮凝工艺条件.结果表明,PZFSiC具有较好的贮存稳定性,在使用PZFSiC时,适应的pH范围广.在实验过程中形成大而致密的絮体,沉降迅速,浑浊度去除率超过98%,COD去除率达93%.处理后的废水,出水水质好,水样澄清透明.在与同类絮凝剂对比实验中,效果优于PZSiC和PFSiC.     

Complexes of fulvic acid on the surface of hematite, goethite, and akaganeite: FTIR observation

The present work extended our knowledge on the binding and complexation of a fulvic acid (FA) derived from leonardite and the iron oxides (hematite, goethite and akaganeite) by Fourier transform infrared spectroscopy (FTIR). As a prerequisite, the iron oxides were firstly prepared and characterized by transmission electron micrograph (TEM). All iron phases were single and well-described crystalloid. The FTIR data obtained by two different sampling preparation methods gave the consisting evidences that under our experimental conditions the interaction mechanism was to the ligand-exchange involving carboxylic functional groups of the FA and the surfaces sites of both hematite and goethite, while no complexation can be evidenced in the case of akaganeite, only surface adsorption. In general, the binding affinities of the iron oxides with the FA was in the order of hematite>goethite>akaganeite. The present method, although associated with some uncertainties, provided an opportunity to increase the knowledge in the field of the humic chemistry.     

海洋沉积物中的天然气水合物与海底滑坡

天然气水合物是一种由天然气和水形成的类似冰状的固体物质 ,主要存在于在低温高压背景下的海底沉积物和陆地永久冻土地带中。赋存于海底沉积物中的天然气水合物虽然本身能作为准稳定的胶结物对海底有建造作用 ,但由于其稳定性对特定温度和压力的严格依赖 ,海平面的下降、海底的连续沉积、地震等自然因素以及海洋钻探等人为因素造成的海底温压条件的改变会引起其分解 ,从而使海底沉积物失稳甚至导致海底滑坡。本文详细介绍了海底天然气水合物分解导致滑坡的机制、实例以及该种海底滑坡体的特征 ,并对以后的研究进行了展望     

Comparison of CNT-PVA membrane and commercial polymeric membranes in treatment of emulsified oily wastewater

CNT-PVA membrane was fabricated and compared with polymeric membranes. The separation performance was evaluated by homemade and cutting fluid emulsions. The three membranes show similar oil retention rates. CNT-PVA membranes have higher permeation fluxes compared with polymeric membranes. CNT-PVA membrane shows higher fouling resistance. Membrane separation is an attractive technique for removal of emulsified oily wastewater. However, polymeric membranes which dominate the current market usually suffer from severe membrane fouling. Therefore, membranes with high fouling resistance are imperative to treat emulsified oily wastewater. In this study, carbon nanotube-polyvinyl alcohol (CNT-PVA) membrane was fabricated. And its separation performance for emulsified oily wastewater was compared with two commercial polymeric membranes (PVDF membrane and PES membrane) by filtration of two homemade emulsions and one cutting fluid emulsion. The results show that these membranes have similar oil retention efficiencies for the three emulsions. Whereas, the permeation flux of CNT-PVA membrane is 1.60 to 3.09 times of PVDF membrane and 1.41 to 11.4 times of PES membrane, respectively. Moreover, after five consecutive operation circles of filtration process and back flush, CNT-PVA membrane can recover 62.3% to 72.9% of its initial pure water flux. However, the pure water flux recovery rates are only 24.1% to 35.3% for PVDF membrane and 6.0% to 26.3% for PES membrane, respectively. Therefore, CNT-PVA membrane are more resistant to oil fouling compared with the two polymeric membranes, showing superior potential in treatment of emulsified oily wastewater.     

Carbon nanotubes-incorporated MIL-88B-Fe as highly efficient Fenton-like catalyst for degradation of organic pollutants

CNTs were incorporated into MIL-88B-Fe to get a new Fenton-like catalyst (C@M). Fe(II) was introduced in C@M to get a fast initiation of Fenton-like reaction. Fe(II) content in C@M was related with oxygen-containing functional groups on CNTs. C@M shows efficient catalytic degradation of pollutants over a wide pH range. Iron-based metal organic frameworks have been verified to be efficient heterogeneous Fenton catalysts due to their open pore channels and highly uniform distribution of metallic centers. In these catalysts, however, the iron element is mainly in the form of Fe(III), which results in a process required to reduce Fe(III) to Fe(II) to initiate Fenton reaction. To address this problem, carbon nanotubes (CNTs) with electron-rich oxygen-functional groups on the surface were incorporated into the metal organic frameworks (MIL-88B-Fe) to improve Fe(II) content for an enhanced Fenton-like performance. The prepared CNT@MIL-88B-Fe (C@M) showed much stronger catalytic ability toward H₂O₂ than MIL-88B-Fe. The pseudo-first-order kinetic constant for phenol degradation by C@M (0.32 min^–1) was about 7 times that of MIL-88B-Fe, and even higher than or comparable to the values of reported heterogeneous Fenton-like catalysts. Moreover, the Fenton-like system could effectively degrade various kinds of refractory organic pollutants and exhibited excellent catalytic activity over a wide pH range (4–9). XPS analysis confirmed that Fe(II) content of the catalyst gradually increased with CNT loadings. Electron spin resonance analysis showed that the signal intensity (•OH) of C@M was much higher than MIL-88B-Fe, which was consistent with the degradation efficiency of pollutants. Furthermore, the Fe(II) content of the catalyst gradually increased along with the oxygen-functional group content of CNTs. The result demonstrated that oxygen-containing functional groups of CNTs have a significant impact on the enhanced catalytic performance of C@M. This study provides a new insight to enhance Fenton reaction by using nanocarbon materials.     

Changes in the heavy metals and petroleum hydrocarbon contents in seawater and surface sediment in the year following artificial reef construction in the Pearl River Estuary,China

Environmental Science and Pollution Research - Marine pollution is an important driver of ocean biodiversity loss, which can be mitigated by the construction of artificial reefs (ARs). Many studies...     

钙镁试剂-示波计时电位法快速测定天然水中不同形态铝

采用钙镁试剂 (CLG) 示波计时电位法 ,分别在中性和碱性条件下直接检测天然水中的无机单核铝 [Ali]和总单核铝 [Ala]浓度 .并用该法测定了酸消化水样中的总铝 [AlT],由 [Ala]-[Ali]间接得到有机单核铝 [Alo],[AlT]-[Ala]得到酸溶态铝 [Alr],从而实现了水中五种Al形态的电化学测定 .实验结果表明 :在pH9 0的 0 5mol·1 - 1KCl+ 0 1mol·1 - 1Na2 B4 O7缓冲溶液中 ,CLG切口为Ep1=-0 75V ,加入铝后出现新切口 ,Ep2 =-0 90V ,检测线性范围为 8× 1 0 - 6— 4× 1 0 - 5mol·1 - 1,检测下限为 6× 1 0 - 7mol·1 - 1,在 3× 1 0 - 5mol·1 - 1Al时 ,相对标准偏差为 4 8% (n =1 0 ) .在中性条件下测定的是无机单核铝 ,而在碱性条件下则是总单核铝 (包括无机单核铝和有机单核铝两部分 ) .     

遮阴和盐分对银叶树幼苗光合特性与叶绿素荧光参数的影响

通过比较不同光和盐水平下银叶树(Heritiera littoralis)幼苗的叶绿素含量、光合光响应参数及叶绿素荧光参数的差异,探讨了遮阴和施盐处理下银叶树幼苗的光合生理及适应能力。以银叶树盆栽幼苗为研究对象,以全光无盐为对照,设置遮阴(遮光率为80%)与2.5%盐水处理,经60 d的处理,测定其光合光响应参数、叶绿素荧光参数及叶绿素含量。结果表明,在正常环境下,银叶树光饱和点(LSP)、光补偿点(LCP)及Chla/b分别为1023、28.8μmol·m^?2·s^?1及3.65,属阳性树种。在无盐条件下,遮阴处理导致了叶片叶绿素含量、表观量子效率(AQY)、PSⅡ潜在活性(Fv/Fo)、PSII最大光化学效率(Fv/Fm)及PSⅡ有效光化学量子产量(Fv'/Fm')的升高,却降低了Chl a/b、最大净光合速率(P′max)、LSP、LCP、暗呼吸速率(Rd)、初始荧光(Fo)、PSⅡ实际光合效率(ΦPSⅡ)、表观光合量子传递效率(ETR)、光化学猝灭系数(qP)及非光化学淬灭系数(NPQ)。在全光照或80%的遮阴环境下,盐胁迫均使得叶片叶绿素含量、光合光响应参数(AQY、P′max、LSP)及叶绿素荧光参数(Fm、Fv/Fo)显著下降(P<0.05);而在全光环境下,盐胁迫同样显著降低了Fv/Fm、ΦPSⅡ、ETR(P<0.05),但在遮阴环境下,盐胁迫并没有显著降低叶片Fv/Fm、Fv′/Fm′、ΦPSⅡ及ETR(P>0.05)。盐分对叶片叶绿素含量、光合光响应参数(AQY、P′max及LSP)及叶绿素荧光参数(Fo、Fm、Fv、Fv/Fo、ΦPSⅡ、ETR及NPQ)的影响高于光照,光和盐对叶绿素含量、光合光响应参数(AQY、P′max及LSP)及叶绿素荧光参数的影响没有交互作用。研究表明,银叶树幼苗表现出较高的耐阴性及对弱光的利用能力;盐胁迫使银叶树幼苗发生了明显的光抑制,PSII的光化学活性降低,过剩光能对光系统的破坏的风险增加,光能转换效率与电子传递能力下降,光合作用效率大幅降低。     

哌嗪氨基二硫代甲酸型螯合树脂的合成及其吸附性能

用哌嗪和二硫化碳反应合成氨基二硫代甲酸中间体，再与二卤代烃反应得到1，4-双(二硫代酯基)哌嗪聚合物，考察了中间体和螯合树脂对Ag^ ，Cu^2 ，Zn^2 ，Ni^2 ，CO^2 ，Pb^2 ，Pd^2 ，Cr^3 的静态吸附性能，结果表明，两者均可以吸附金属离子，缩聚后的螯合树脂具有更强的吸附能力。