基于PMF模型的农田土壤重金属源暴露风险综合评价:以浙江省某电子垃圾拆解区为例

为探究农田土壤重金属污染特征、来源及其人体健康风险,为农田污染治理提供重要科学依据,采集了浙江省典型电子垃圾拆解区周边农田133个表层（0~20 cm）土壤样本,测定了土壤Cd、Pb、Cr、Cu、Zn、Ni、As和Hg含量,运用多种方法评价重金属污染程度及生态风险,采用正定矩阵因子分解法（PMF）融合地统计学,解译污染来源及定量各个污染源的贡献度,将源解析结果和人体健康风险评价模型相结合,从来源暴露角度评价了各个污染源对人体健康的风险.结果表明,ω（Cd）、ω（Pb）、ω（Cr）、ω（Cu）、ω（Zn）、ω（Ni）、ω（As）和ω（Hg）平均值：0.76、65.22、92.02、103.92、198.49、36.65、5.97和0.20 mg ·kg^-1,Cd和Cu含量平均值均高于农用地土壤污染风险筛选值,点位污染占比分别为85.71%和96.24%.Pb、Cr、Zn和Ni含量平均值超过浙江省温黄平原土壤背景值,As和Hg在限值内.污染评价结果表明,土壤综合潜在生态风险以轻-中度为主,占比达90.98%,较高和高度风险占比都为4.51%,Cd为主要潜在生态风险元素.研究区重金属污染来源主要为电子垃圾拆解工序污染源（26.82%）、燃煤及交通排放混合源（34.50%）、自然母质及农业投入混合源（25.59%）和电子垃圾酸洗径流及固废淋溶来源（13.09%）.儿童重金属暴露健康风险显著大于成年人,自然母质和农业投入混合源对人体健康风险贡献最多,Cr是对人体健康风险影响最大的元素.     

海南岛半干旱区农用地土壤重金属富集因素、健康风险及来源识别

为了解海南岛半干旱区农业土壤中重金属富集因素和污染状况,在感城镇采集1818件表层土壤样品,测定其重金属含量和化学组成.采用相关分析、地累积指数（I_geo）、综合生态风险指数（RI）、危害指数（HI）、致癌风险指数（CR）和正定矩阵因子分析（PMF）开展重金属风险评价和来源识别.结果显示,重金属ω（As）、ω（Cd）、ω（Cr）、ω（Cu）、ω（Hg）、ω（Ni）、ω（Pb）和ω（Zn）的平均值分别为22.7、0.128、33.4、14.5、0.032、9.32、32.5和43.3 mg ·kg^-1,除Zn外,均高于海南岛土壤背景值.相关分析表明,重金属富集与土壤中Fe、Mn、Al和有机质含量密切相关.I_geo结果表明,研究区农业土壤主要受到As的污染,其次为Cd和Cu;RI结果显示,高风险以上的样品占比为29.4%,其中As是潜在生态风险的主要贡献者;健康风险评估结果显示,As、Cr和Ni对儿童存在致癌风险,需要引起注意.基于PMF模型,确定了研究区重金属的4种主要来源,其中Hg主要来自工业排放;As主要来自农业活动;Ni、Cu、Cr和Zn主要来自与成土母质密切相关的自然来源;Pb和Cd主要来自农业活动和机动车尾气的混合源.研究表明PMF模型与相关分析相结合,能够有效识别土壤重金属来源.     

基于PMF模型的县域尺度土壤重金属来源分析及风险评价

为探究小尺度空间区域土壤重金属的污染特征、风险和来源,以广东省揭阳市榕城区为例,运用富集系数、污染负荷指数、生态风险评价模型、健康风险评价模型进行风险评价,结合相关性分析、空间分析和正定矩阵因子分解（PMF）模型进行来源解析.结果表明,土壤中ω（Cr）、ω（Hg）、ω（As）、ω（Pb）、ω（Ni）、ω（Cd）、ω（Cu）和ω（Zn）的均值分别为54.87、0.25、8.35、56.00、15.38、0.35、30.56和124.23 mg ·kg^-1,均超过广东省土壤背景值;Cr、As、Pb和Ni无富集,Zn和Cu轻微富集,Hg和Cd中等富集;污染负荷指数的均值为2.37,总体上属于重度污染水平,8种元素处于不同的污染水平.研究区土壤重金属整体处于重度生态风险,其中Hg和Cd属于强烈生态风险,其他元素属于轻微生态风险.不同元素在3种暴露途径下产生的非致癌风险处于可接受范围;成人和儿童的致癌风险分别为9.81E-05和5.59E-04,Cr和As是致癌风险的主要贡献者,需重点关注.研究区土壤重金属共有4种主要来源：交通来源（37.02%）、成土母质来源（18.53%）、大气沉降来源（26.49%）和工业来源（17.96%）.     

黄河下游悬河段饮用水源地土壤重金属污染、来源及健康风险

选择黄河下游典型悬河段饮用水源地（黑池和柳池）土壤为研究对象,运用地累积指数与污染负荷指数分析7种（Cr、Ni、Cu、Zn、Cd、Pb和As）重金属污染特征,运用相关性分析和主成分分析等定性和绝对因子得分-多元线性回归（APCS-MLR）定量相结合的方法开展源解析,利用美国环保署（USEPA）推荐的健康风险评价模型分析土壤重金属对人体健康影响,并结合APCS-MLR模型分析污染源对健康风险的贡献率.结果表明,水源地周边土壤重金属ω（Cr）、ω（Ni）、ω（Cu）、ω（Zn）、ω（Cd）、ω（Pb）和ω（As）的均值依次为60.27、30.00、35.14、77.75、0.38、21.74和9.70 mg·kg^-1,除As外,元素Cr、Ni、Cu、Zn、Cd和Pb含量均高于黄河下游潮土区土壤元素背景值,而柳池周围土壤Cu和Zn含量明显高于黑池,其他重金属含量差别较小;地累积指数与单因子指数均显示黑池和柳池存在重金属轻度污染,Cd是主要的污染因子,污染负荷指数模型显示研究区无污染和轻度污染样点数分别占总样点数的5%和95%,表明研究区整体处于轻度污染水平;源解析表明Cr、Ni、Cu和As主要受成土母质影响;APCS-MLR模型解析结果表明,研究区土壤污染物主要来自自然源、交通源、农业源和未知源,其来源贡献率依次为42.95%、23.39%、16.95%和16.71%;健康风险评价模型结果显示,重金属对成人和儿童无非致癌风险,存在人体可耐受的致癌风险,儿童的非致癌风险和致癌风险均高于成人.As为主要非致癌因子,Ni为主要致癌因子.无论是成人或儿童,4种污染源的非致癌和致癌风险贡献率均为：自然源>未知源>交通源>农业源,其中自然源对非致癌和致癌风险贡献率最大.因此研究黄河下游悬河段水源地周边土壤污染特征、来源及对人体健康影响,对于水源地保护具有重要意义,同时为黄河沿线生态环境高质量发展提供理论支撑.     

基于源导向和蒙特卡洛模型的广东省某城市土壤重金属健康风险评估

以广东省某市为研究区域,通过研究其表层土壤重金属含量及空间分布特征,明确土壤重金属污染情况和优先控制因子,为该市土壤重金属污染防治提供基础数据.对该市221个土壤样品中的重金属含量特征进行分析,并通过潜在健康风险评估（HRA）模型、PMF受体模型和蒙特卡洛模型进行潜在健康风险评估、来源解析和主控因子分析.结果发现,该市土壤重金属ω（As）、ω（Hg）、ω（Cd）、ω（Pb）、ω（Cr）、ω（Cu）、ω（Ni）和ω（Zn）的平均值分别为18.16、0.43、1.46、68.57、98.34、64.19、26.53和257.32 mg·kg^-1,变异程度为中高度变异.除Ni元素以外,土壤其余重金属元素含量均已一定程度超过广东省土壤背景值,且Cd和Zn的含量已超过国家二级标准,重金属污染已较为严重;重金属来源主要为工业源,自然母质、铅蓄电池制造、交通、人为耕作和农药化肥投入也对土壤重金属累积有不可忽视的影响;土壤重金属对儿童和成人均存在一定程度的可耐受致癌健康风险,非致癌风险可以忽略不计;儿童的潜在健康风险大于成人,主要暴露途径均为经口摄入;农药化肥投入源和As应该作为该市土壤重金属影响健康风险的主控因子,其次为混合源和Cr;重金属空间分布特征及相对污染程度存在差异,应深化分区监测管控,加强土壤的污染防治,减少土壤重金属的人为输入.     

湘西地区土壤重金属污染溯源分析及环境质量评价

为探究湘西地区土壤重金属污染状况及环境质量综合情况,选择凤凰县相关区域作为研究区,于2022年6~8月在研究区采集440件表层土壤样品,分析土壤中的As、Cd、Cr、Cu、Hg、Ni、Pb和Zn这8种重金属元素以及测定土壤pH值.采用PMF模型进行溯源分析,并结合GIS技术开展土壤环境质量地球化学评价.结果表明,研究区土壤以弱酸性为主,重金属ω（Zn）、ω（Cr）、ω（Pb）、ω（Ni）、ω（Cu）、ω（As）、ω（Cd）和ω（Hg）平均值依次为：81.02、64.67、31.63、29.27、25.52、9.93、0.28和0.13 mg·kg^-1,Cd和Hg元素相对全国土壤背景值较高,且呈高度变异,林地中的Hg和Cd元素含量高于其他土地利用.PMF模型结果表明,研究区土壤重金属污染来源贡献率依次为矿区开采源（37.4%）、大气沉降源（7.7%）、自然源（41.1%）和农业活动源（13.8%）,并根据4类污染源空间分布提供了污染管控措施建议,通过土壤环境地球化学综合评价将研究区分为3类地块,分别为无风险地区（94.27 km²）,占比为76.38%;风险可控区（27.45 km²）,占比为22.24%;风险较高区（1.7 km²）,占比为1.38%.为该研究区土地污染的防治措施和防治范围划区等提供数据支撑.     

中国农田土壤重金属污染分析与评价

为掌握中国农田土壤八大重金属元素（As、Cd、Cr、Cu、Hg、Ni、Pb和Zn）的污染现状,探究其时空变化和在不同耕地类型之间的差异,通过中国知网和Web of Science收集并整理了2005~2021年449篇相关文献数据,采用基于“样点数”、“研究区面积”和“标准差”的加权方式进行Meta分析.结果显示,中国农田土壤八大重金属的含量平均值为：ω（As）11.00 mg·kg^-1、ω（Cd）0.350 2 mg·kg^-1、ω（Cr）62.91 mg·kg^-1、ω（Cu）28.87 mg·kg^-1、ω（Hg）0.135 1 mg·kg^-1、ω（Ni）28.91 mg·kg^-1、ω（Pb）34.67 mg·kg^-1和ω（Zn）90.24 mg·kg^-1.与土壤背景值相比,中国农田土壤中各重金属元素（除As外）均存在一定累积,其中Cd和Hg的累积量最大,分别超过对应土壤背景值177.9%和340.3%.污染评价结果表明,我国农田土壤重金属污染以Cd和Hg为主,人类活动是造成其在土壤中累积的主要影响因子;从时空变化上看,云贵高原和东部沿海是污染案例最集中的区域,污染重心随时间变化由长江中游向西南地区偏移;不同耕地类型之间土壤重金属含量存在差异,蔬菜地和水田中重金属的累积量明显大于其他耕地类型.     

湘东北典型河源区土壤重金属分布特征、来源解析及潜在生态风险评价

水源地土壤环境质量状况关乎其流域内居民生命健康安全,是生态环境保护研究中的热点科学问题.选择湘东北典型河源区,采集表层土壤样品共87件,通过GIS技术和潜在生态风险指数法研究了土壤重金属（Cd、Pb、Cr、Hg和As）的空间分布特征和潜在生态风险,并采用多元统计分析和正定矩阵因子分解（PMF）模型解释了其可能来源和贡献率.结果表明：①湘东北典型河源区土壤呈酸性,土壤重金属ω（Cd）、ω（Pb）、ω（Cr）、ω（Hg）和ω（As）平均值分别为0.20、41.07、130.51、0.29和11.63mg ·kg^-1,对标背景值,除As外均有富集;②土壤重金属综合潜在生态风险为中等风险等级,其中Cr、Pb和As为轻微风险等级,Cd和Hg均为强风险等级;③土壤Cd和Pb具有同源性,主要来源于农业活动,Cr和As受生活垃圾排放和自然母质的双重影响,Hg主要来源于化石燃烧及交通运输;④生活垃圾排放源、自然母质源、化石燃烧及交通运输源和农业活动源对湘东北典型河源区土壤重金属的贡献率分别为21.36%、35.92%、19.30%和23.42%,人为源贡献率大于自然源.研究结果对湘东北典型河源区的污染防治、生态修复和美丽乡村建设具有参考价值.     

石家庄市栾城区农田土壤重金属分布特征及作物风险评价

为探讨栾城区内农田土壤重金属的分布特征,对表层土壤As、Cd、Cr、Cu、Hg、Ni、Pb和Zn这8种重金属污染特征、空间分布和污染风险进行分析,并使用PMF模型进行污染源解析,探讨栾城区土壤管控方案.进一步检测作物中重金属含量,利用概率风险评价方法评价研究区农产品的非致癌健康风险,为栾城区内农田土壤重金属污染治理与防控提供理论基础.结果表明,表层土壤ω（Cd）、ω（Cr）、ω（Cu）、ω（Pb）和ω（Zn）分别为0.06~1.08、22.14~473.47、12.83~150.74、10.75~577.72和62.23~652.78 mg·kg^-1,点位超标率分别为1.83%、1.22%、0.61%、0.61%和1.22%.此外,部分区域土壤中的重金属有向作物中转移并积累的现象,小麦籽粒Cd和Pb含量超标率分别为2.13%和5.32%,玉米籽粒Cd含量超标率为1.20%.健康风险评价结果表明,栾城区玉米的复合非致癌健康风险（TTHQ）小于1,对人体没有明显的负面影响,食用研究区小麦的复合非致癌风险（TTHQ>1）,对人体产生负面影响的可能性较大.土壤中重金属的空间分布受工业区涉污企业分布的影响,8种重金属含量较高的区域均主要分布在工业企业较集中的中部、西部和南部.总体而言,研究区大部分表层耕地土壤未受到明显的重金属污染,存在中等强度（2级）的生态危害.Cd为无-中度污染（1级）,Cd和Hg存在中等强度潜在生态风险（2级）,其余重金属均为无污染,低潜在生态风险（1级）.根据PMF污染源解析结果和实地调查推测,土壤重金属主要来自土壤母质（52.05%）,历史污灌和工业生产的人为污染源（32.98%）和大气沉降（14.97%）.综上所述,研究区北部和东部土壤重金属含量较低,应划分为优先保护类,研究区西部、中部和南部部分点位重金属含量超标,其来源主要为化工、涂料、机械装备等企业,应划分为安全利用类,严控污染物的输入,采用农艺调控等措施,减少重金属向农作物的转移,降低食品安全健康风险.本研究将有助于栾城区土壤的分级治理和污染管控.     

乌鲁木齐市安宁渠蔬菜基地土壤重金属污染现状及潜在生态风险评价

为了认识蔬菜产地土壤重金属富集现状，探索其解决途径，为污染防治措施提供科学依据，促进无公害蔬菜生产，确保蔬菜质量安全。在乌鲁木齐北郊蔬菜地采集26个土壤样品和7个水体样品，分别测定样品中Hg、As、Cr、Cd、Pb和Zn 6种重金属的含量。采用地积累指数（I_geo）、污染负荷指数（PLI）、潜在生态风险评价（RI）对蔬菜地土壤重金属污染及潜在生态风险进行分析。通过土壤与水样的结合，采用主成分分析法进行污染来源分析，结果表明：（1）乌鲁木齐安宁渠蔬菜基地土壤中Hg、Cr和Zn重金属含量的均值分别为新疆土壤背景值的5.74、1.74、1.52倍，其中Cd含量的均值是国家二级标准的2.69倍。地下水中Cr含量均值超过国家灌溉水限制标准，是其8.89倍。（2）6种重金属I_geo的平均值依次为Cd > Hg > Cr > Zn > As > Pb，其中Cd属于中-强度污染，Hg为中度污染，Cr为轻度污染，Zn、As和Pb均为清洁水平。研究区土壤区域污染负荷指数PLI_zone为1.91，属于中度污染，其中Cd的贡献率最大，为56%，其次是Hg，贡献率为22%。土壤RI均值为673.1，属于严重潜在生态风险态势。（3）研究区土壤Pb、Cr和Zn，主要来自交通和农业活动等人为污染，As、Cd主要受自然母质和大气沉降的影响。该蔬菜基地潜在生态风险主要来自Cd和Hg，建议在农业生产中防范Cd、Hg的污染。     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.