TiO_2/NiPECO体系降解DMP的动力学和光电协同作用研究

以采用微波辅助法制备的TiO2/Ni光电极为阳极,纤维状石墨毡材料(graphite felt,GF)为阴极,饱和甘汞电极(saturated calomel electrode,SCE)为参比电极建立TiO2/Ni光电催化氧化(PECO)体系.以邻苯二甲酸二甲酯(dimethyphthalate,DMP)为目标物,研究其光电催化降解反应动力学和光电协同作用.结果显示:DMP的降解符合拟一级动力学规律;当DMP初始浓度一定时,影响DMP光电催化降解速率的因素由强到弱依次为:催化剂有效面积,紫外光强度,曝氧速率,外加偏转电压等.实验证明本体系中光电之间具有协同作用.     

Institutional, policy and farmer responses to drought: El Niño events and rice in the Philippines

Droughts are common recurring natural hazards in Asia, and El Niño events are particularly severe in the Philippines. This paper explores responses by farm households, irrigation system managers, and macro policymakers in the Philippines to El Niño. In response to the large 1997–98 El Niño, farmers in one major irrigation system significantly diversified their economic activities, hut the drought was so acute that many of these activities were not successful. Communication between meteorologists and irrigation system managers is strong, and irrigation system managers are aware of El Niño events in advance. Communication between irrigation system managers and farmer irrigation associations is also strong, and together they have developed response options that attempt to augment supplies of and more efficiently allocate scarce water. Water pricing is not used, however, and lack of cooperation among farmers results in sub-optimal outcomes. Macro-level policy responses in terms of rice imports and buffer stock management to protect poor consumers have improved substantially over time.     

Dechlorination of chlorinated hydrocarbons by bimetallic Ni/Fe immobilized on polyethylene glycol-grafted microfiltration membranes under anoxic conditions

In this study, the dechlorination of chlorinated hydrocarbons including trichloroethylene (TCE), tetrachloroethylene (PCE) and carbon tetrachloride (CT) by bimetallic Ni/Fe nanoparticles immobilized on four different membranes was investigated under anoxic conditions. Effects of several parameters including the nature of membrane, initial concentration, pH value, and reaction temperature on the dechlorination efficiency were examined. The scanning electron microscopic images showed that the Ni/Fe nanoparticles were successfully immobilized inside the four membranes using polyethylene glycol as the cross-linker. The agglomeration of Ni/Fe were observed in poly(vinylidene fluoride), Millex GS and mixed cellulose ester membranes, while a relatively uniform distribution of Ni/Fe was found in nylon-66 membrane because of its hydrophilic nature. The immobilized Ni/Fe nanoparticles exhibited good reactivity towards the dechlorination of chlorinated hydrocarbons, and the pseudo-first-order rate constant for TCE dechlorination by Ni/Fe in nylon-66 were 3.7-11.7 times higher than those in other membranes. In addition, the dechlorination efficiency of chlorinated hydrocarbons followed the order TCE > PCE > CT. Ethane was the only end product for TCE and PCE dechlorination, while dichloromethane and methane were found to be the major products for CT dechlorination, clearly indicating the involvement of reactive hydrogen species in dechlorination. In addition, the initial rate constant for TCE dechlorination increased upon increasing initial TCE concentrations and the activation energy for TCE dechlorination by immobilized Ni/Fe was 34.9 kJ mol⁻¹, showing that the dechlorination of TCE by membrane-supported Ni/Fe nanoparticles is a surface-mediated reaction.     

Removal of Ni(II) and Cu(II) ions using native and acid treated Ni-hyperaccumulator plant Alyssum discolor from Turkish serpentine soil

Alyssum discolor biomass was collected from serpentine soil and was used for removal of metal ions. The plant species grown on serpentine soils are known to be rich with metals ions and thus have more capability for accumulating heavy metals. Native and acid-treated biomass of A. discolor (A. discolor) were utilized for the removal of Ni(II) and Cu(II) ions from aqueous solutions. The effects of contact time, initial concentration, and pH on the biosorption of Ni(II) and Cu(II) ions were investigated. Biosorption equilibrium was established in about 60 min. The surface properties of the biomass preparations were varied with pH, and the maximum amounts of Ni(II) and Cu(II) ions on both A. discolor biomass preparations were adsorbed at pH 5.0. The maximum biosorption capacities of the native, and acid-treated biomass preparations for Ni(II) were 13.1 and 34.7 mg g⁻¹ and for Cu(II) 6.15 and 17.8 mg g⁻¹ dry biomass, respectively. The biosorption of Ni(II) and Cu(II) ions from single and binary component systems can be successfully described by Langmuir and Freundlich isotherms. When the heavy metal ions were in competition, the amounts of biosorbed metal ions on the acid treated plant biomass were found to be 0.542 mmol g⁻¹ for Ni(II) and 0.162 mmol g⁻¹ for Cu(II), the A. discolor biomass was significantly selective for Ni(II) ions. The information gained from these studies was expected to indicate whether the native, and acid-treated forms can have the potential to be used for the removal and recovery of Ni(II) ions from wastewaters.     

Catalytic reductive dechlorination of p–chlorophenol in water using Ni/Fe nanoscale particles

Nanoscale bimetallic Ni/Fe particles were synthesized from the reaction of sodium borohydride （NaBH4） with reduction of Ni^2＋ and Fe^2＋ in aqueous solution. The obtained Ni/Fe particles were characterized by TEM （transmission electron microscope）, XRD （X-ray diffractometer）, and N2-BET. The dechlorination activity of the Ni/Fe was investigated using p-chlorophenol （p-CP） as a probe agent. Results demonstrated that the nanoscale Ni/Fe could effectively dechlorinate p-CP at relatively low metal to solution ratio of 0.4 g/L （Ni 5 wt%）. The target with initial concentration ofp-CP 0.625 mmol/L was dechlorinted completely in 60 rain under ambient temperature and pressure. Factors affecting dechlorination efficiency, including reaction temperature, pH, Ni loading percentage over Fe, and metal to solution ratio, were investigated. The possible mechanism of dechlorination ofp-CP was proposed and discussed. The pseudo-first- order reaction took place on the surface of the Ni/Fe bimetallic particles, and the activation energy of the dechlorination reaction was determined to be 21.2 kJ/mol at the temperature rang of 287-313 K.     

洪泽湖流域洪涝灾害演变趋势及其与El Ni(n)o事件关系

为分析洪泽湖流域洪涝灾害在千年尺度序列上的演变趋势,采用统计历史洪涝记录的方法,分析了气候变化背景下洪涝灾害的响应过程,探讨了洪泽湖流域洪涝灾害同El Ni(n)o事件的关系.结果表明:近1 000 a来洪泽湖流域洪涝灾害的频度总体是趋于上升的,这种变化趋势同气候变化的趋势是一致的.研究结果显示:公元1000～1400年洪涝记录偏少,同我国东部地区尤其是中世纪暖期出现的一次200 a以上的干旱化过程有较好的对应性.1400～1800年是洪泽湖流域洪涝的多发期,这一事实同我国东部1550～1850年小冰期期间总体偏湿的环境特征相一致.分析洪涝灾害变化同El Ni(n)o事件对应性关系表明:在El Ni(n)o事件年及其次年是洪泽湖流域洪涝的多发年份.这可能是由于El Ni(n)o事件通过改变西太平洋副高的强度与位置,以及大气环流形势而引起的降水异常所致.了解洪泽湖流域洪涝的演变趋势及其同El Ni(n)o的关系对于长期防灾减灾策略具有重要的参考意义.     

Natural radionuclides distribution and environmental impacts of ferruginous sand-siltstone (raw material) and their manufactured Ahmer oxide used as wall paints

Commercially known Ahmer oxide paints are prepared from raw material mainly composed of red iron oxides (hematite) and iron oxyhydroxides. The raw material used in manufacturing of Ahmer oxide comes from some localities in southwest Sinai such as Abu Thor, Allouga, and El lehian. The adsorption of uranium and other radioelements on iron oxides could make the raw material (red iron oxides) and their products environmentally hazardous. The studied samples were subjected to radiometric analysis using NaI (Tl) gamma-ray spectrometer. The average activity concentration of U, Th, Ra, and K are 108.7, 458.8, 88.8, and 627.5?Bq?kg^?1, respectively in raw material and 136.4, 14.6, 58.3, and 95.9?Bq?kg^?1 in Ahmer oxide. High values of activity concentrations of ²³⁸U, ²²⁶Ra, and ⁴⁰K were recorded in Allouga and El lehian raw material. High radioactivities of Allouga and El lehian raw material are mainly attributed to the presence of torbernite, zircon, and monazite, in addition to adsorbed elemental uranium in Ahmer oxide. absorbed dose rate (D), annual effective dose equivalent, radium equivalent activity (Ra_eq), external hazard index (H_ex), and internal hazard index (H_in), as well as representative gamma index (Iγ) were determined from the activity concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K. Some of the studied samples do not satisfy the universal standards.     

载铁ACF/Ni阴极电化学体系除藻效能与机制

采用化学浸渍法将Fe@Fe₂O₃纳米线负载在活性炭纤维/泡沫镍上组成Fe@Fe₂O₃/ACF/Ni复合阴极,以钛基铂（Pt/Ti）为阳极,考察载铁量、初始pH值和不同电化学体系对除藻效果的影响,探究无供氧条件下Pt/Ti-Fe@Fe₂O₃/ACF/Ni电化学体系除藻的效能;基于·OH间接检测、铁离子浓度、H₂O₂浓度及pH值的分析和·O₂^-的检测研究Pt/Ti-Fe@Fe₂O₃/ACF/Ni中性电化学体系反应机制.结果表明,当制备阴极阶段投加0.03g FeCl₃×6H₂O,初始藻浓度为0.7×10⁹~0.8×10⁹个/L,电流密度为75mA/cm²,初始pH6.2时,电解60min,该体系除藻率可达到92.3%.在Pt/Ti-Fe@Fe₂O₃/ACF/Ni电化学体系中,Fe@Fe₂O₃/ACF/Ni阴极可通过电化学反应产生大量·OH和·O₂^-,使藻细胞破裂死亡;该体系除藻的主要机理是非均相电Fenton反应.     

臭氧预破络-重金属捕集耦合体系高效去除废水中络合态镍的机理研究

电镀废水处理厂化学镀镍废水经常规物化处理后,仍存在低浓度、高稳态的重金属污染物,导致后续出现难处理、难生化、难达标排放的普遍技术问题.本文提出一种新型高效的臭氧预氧化破络-重金属捕集螯合深度处理技术体系,即臭氧-重金属捕集剂(O_3-SN-9)耦合体系.通过单因素静态实验,重点考察了臭氧(O_3)氧化初始pH值、氧化时间、臭氧载气流量、重金属捕集剂(SN-9)投加量等对出水总镍(Ni)去除率的影响,并探讨了臭氧氧化破络络合态Ni的途径及SN-9捕集重金属Ni的机理.结果表明,在化学镀镍废水初始总Ni浓度为2.76 mg·L~(-1),臭氧预氧化初始pH值范围为7.0～11.0,反应时间为40 min,载气流量为3 L·min~(-1),SN-9投加量为40 mg·L~(-1)的条件下,处理后出水总Ni浓度稳定低于0.1 mg·L~(-1),可达到《电镀水污染物排放标准》(DB44/1597—2015)水污染物特别排放限值中总Ni的排放限值要求.液相色谱-质谱(LC-MS)、叔丁醇(Tert-Butyl Alcohol,TBA)捕获羟基自由基(·OH)实验和傅里叶变换红外光谱(FTIR)分析表明,在臭氧预氧化破络与螯合捕集Ni前后协同耦合的高效体系中,前端臭氧氧化以间接氧化为主,直接氧化为辅;氧化进程可控制为部分氧化破络,将高稳态镍络合物氧化成易失稳的小分子Ni络合物及部分离子态Ni;后续SN-9高效螯合捕集Ni的主要官能团为巯基官能团(—SH),可从低分子易失稳的Ni络合物上竞争夺取Ni离子,或直接与游离态Ni(II)反应,形成稳定的四边形配位螯合沉淀物,从而达到去除Ni的目的.     

江蓠对水体重金属铅镍的蓄积及生物修复研究

以活体细基江篱繁枝变型(Gracilariatunuistipitata var)作为研究材料,以Pb、Ni重金属离子为污染因子,通过室内静态模拟实验,综合利用等离子发射光谱仪,超速离心机.差速离心机等实验手段研究在单一离子污染胁迫下,江蓠对Pb、Ni重金属离子的短期去除效果,各重金属离子在其体内蓄积效应,江蓠质外体、...