纳米材料在砷水处理中的应用

本文综述了纳米吸附材料在砷的水处理研究中的应用.纳米吸附剂包括氧化铝、氧化铈、氧化锆、二氧化钛、铁及其氧化物等以及它们的复合纳米材料.     

Applying chemical sedimentation process in drinking water treatment plant to address the emergent arsenic spills in water sources

Arsenic (As) spills occurred more frequently and sometimes polluted water sources in recent years in China. It is as urgent need to develop emergency treatment technologies to address the arsenic threat for large-scale water treatment plants. In response, we developed a chemical sedimentation technology to remove arsenic contaminants for water treatment plants. Bench-scale experiments were conducted to investigate the efficiency of arsenic removal and the influencing factors of the chemical sedimentation treatment process. The influencing factors included the choice and dosage of coagulants, the valence of arsenic and pH value of solution. The As(V) contaminants can be almost completely removed by ferric or alum coagulants. The As(III) contaminants are more recalcitrant to chemical sedimentation, 75% for ferric coagulant and 40% for alum coagulant. The quantitative results of arsenic removal load by different ferric or alum coagulants were presented to help determine the parameters for arsenic treatment technology. The dominant mechanism for arsenic removal is static combination, or adsorption of negative arsenic species onto positive ferric hydroxide or alum hydroxide flocs. The efficiency of this treatment technology has also been demonstrated by a real production test in one water treatment plant with arsenic-rich source water and one emergency response. This technology was verified to be quick to set-up, easy to operate and highly efficient even for high concentration of arsenic.     

Heavy metals,occurrence and toxicity for plants: a review

Metal contamination issues are becoming increasingly common in India and elsewhere, with many documented cases of metal toxicity in mining industries, foundries, smelters, coal-burning power plants and agriculture. Heavy metals, such as cadmium, copper, lead, chromium and mercury are major environmental pollutants, particularly in areas with high anthropogenic pressure. Heavy metal accumulation in soils is of concern in agricultural production due to the adverse effects on food safety and marketability, crop growth due to phytotoxicity, and environmental health of soil organisms. The influence of plants and their metabolic activities affects the geological and biological redistribution of heavy metals through pollution of the air, water and soil. This article details the range of heavy metals, their occurrence and toxicity for plants. Metal toxicity has high impact and relevance to plants and consequently it affects the ecosystem, where the plants form an integral component. Plants growing in metal-polluted sites exhibit altered metabolism, growth reduction, lower biomass production and metal accumulation. Various physiological and biochemical processes in plants are affected by metals. The contemporary investigations into toxicity and tolerance in metal-stressed plants are prompted by the growing metal pollution in the environment. A few metals, including copper, manganese, cobalt, zinc and chromium are, however, essential to plant metabolism in trace amounts. It is only when metals are present in bioavailable forms and at excessive levels, they have the potential to become toxic to plants. This review focuses mainly on zinc, cadmium, copper, mercury, chromium, lead, arsenic, cobalt, nickel, manganese and iron.     

Construction of MOFs-based nanocomposite membranes for emerging organic contaminants abatement in water

● Application of the MOF-composite membranes in adsorption was discussed. ● Recent application of MOFs-membranes for separation was summarized. ● Separation and degradation for emerging organic contaminants were described. Presence of emerging organic contaminants (EOCs) in water is one of the major threats to water safety. In recent decades, an increasing number of studies have investigated new approaches for their effective removal. Among them, metal-organic frameworks (MOFs) have attracted increasing attention since their first development thanks to their tunable metal nodes and versatile, functional linkers. However, whether or not MOFs have a promising future for practical application in emerging contaminants-containing wastewater is debatable. This review summarizes recent studies about the removal of EOCs using MOFs-related material. The synthesis strategies of both MOF particles and composites, including thin-film nanocomposite and mixed matrix membranes, are critically reviewed, as well as various characterization technologies. The application of the MOF-based composite membranes in adsorption, separation (nanofiltration and ultrafiltration), and catalytic degradation are discussed. Overall, literature survey shows that MOFs-based composite could play a crucial role in eliminating EOCs in the future. In particular, modified membranes that realize separation and degradation might be the most promising materials for such application.     

Efficient removal of heavy metals from electroplating wastewater using polymer ligands

Poly(hydroxamic acid)-poly(amidoxime) chelating ligands were synthesized from poly(methyl acrylate-co-acrylonitrile) grafted acacia cellulose for removing toxic metal ions from industrial wastewaters. These ligands showed higher adsorption capacity to copper (2.80 mmol?g⁻¹) at pH 6. In addition, sorption capacities to other metal ions such as iron, zinc, chromium, and nickel were also found high at pH 6. The metal ions sorption rate (t_1/2) was very fast. The rate of adsorption of copper, iron, zinc, chromium, nickel, cobalt, cadmium and lead were 4, 5, 7, 5, 5, 8, 9 and 11 min, respectively. Therefore, these ligands have an advantage to the metal ions removal using the column technique. We have successfully investigated the known concentration of metal ions using various parameters, which is essential for designing a fixed bed column with ligands. The wastewater from electroplating plants used in this study, having chromium, zinc, nickel, copper and iron, etc. For chromium wastewater, ICP analysis showed that the Cr removal was 99.8% and other metal ions such as Cu, Ni, Fe, Zn, Cd, Pb, Co and Mn removal were 94.7%, 99.2%, 99.9%, 99.9%, 99.5%, 99.9%, 95.6% and 97.6%, respectively. In case of cyanide wastewater, the metal removal, especially Ni and Zn removal were 96.5 and 95.2% at higher initial concentration. For acid/alkali wastewater, metal ions removing for Cd, Cr and Fe were 99.2%, 99.5% and 99.9%, respectively. Overall, these ligands are useful for metal removal by column method from industrial wastewater especially plating wastewater.     

Strategies to design modified activated carbon fibers for the decontamination of water and air

The rapid industrialization has induced the entry of organic and inorganic contaminants into the environment at a rate greater than environmental cleaning. As a consequence, pollutants have accumulated in environmental media, thus posing health risk for living organisms. Here, we present surface treatment strategies that modify physicochemical properties of activated carbon fibers for environmental remediation. In particular, we review metals, metal oxides and various advanced materials used for modifying activated carbon fibers. We discuss the utilization of modified activated carbon fibers for adsorption of organic pollutants and inorganic pollutants, and for the degradation of organic pollutants by photocatalysis, electrocatalysis, Fenton process and dielectric barrier discharge. We also discuss air pollutant removal, capacitive deionization, removal of inorganic ions and microbial decontamination by modified activated carbon fibers.     

Health Risks Associated with Contamination of Groundwater by Abandoned Mines Near Twisp in Okanogan County, Washington, USA

Abandoned mines are known to contaminate private drinking water wells with toxic metals and arsenic (As). Little attention is given, however, to sites in rural areas with low population densities where natural, geogenic sources of contaminants might also occur. This study measured arsenic and trace element exposure among residents consuming water from wells adjacent to abandoned mines near Twisp, in Okanogan County, Washington, USA, estimated the risk of adverse health effects, and considered the degree of uncertainty associated with the assessed risk. Water samples were collected between October 1999 and June 2001. Average As concentrations ranged from <1 to 298 microg L(-1), lead (Pb) ranged from 0 to 94 microg L(-1), cadmium (Cd) 0-5 microg L(-1), and selenium (Se) 0-390 microg L(-1). Concentrations varied seasonally with maximum concentrations occurring in conjunction with snow-melt. The calculated risk of mortality from cancer following exposure to As at average concentrations as low as 8 microg L(-1) was greater than one in 10,000. Additional noncarcinogenic risks are associated with exposure to As, Cd, Pb and Se. A potentially affected population, estimated to be between 1000 and 1287 residents, live within a 6.5-km (4-mile) radius of the study site. This study emphasises the need to test drinking water wells in the vicinity of abandoned mines during times of maximum snow-melt to determine the extent of risk to human health. Residents drinking water from wells tested in this study who want to reduce the estimated carcinogenic risk and the noncarcinogenic hazard quotient should consider treating their water or find alternative sources.     

Arsenic uptake by plants and possible phytoremediation applications: a brief overview

This review focuses the behaviour of arsenic in plant?Csoil and plant?Cwater systems, arsenic?Cplant cell interactions, phytoremediation, and biosorption. Arsenate and arsenite uptake by plants varies in different environment conditions. An eco-friendly and low-cost method for arsenic removal from soil?Cwater system is phytoremediation, in which living plants are used to remove arsenic from the environment or to render it less toxic. Several factors such as soil redox conditions, arsenic speciation in soils, and the presence of phosphates play a major role. Translocation factor is the important feature for categorising plants for their remediation ability. Phytoremediation techniques often do not take into account the biosorption processes of living plants and plant litter. In biosorption techniques, contaminants can be removed by a biological substrate, as a sorbent, bacteria, fungi, algae, or vascular plants surfaces based on passive binding of arsenic or other contaminants on cell wall surfaces containing special active functional groups. Evaluation of the current literature suggests that understanding molecular level processes, and kinetic aspects in phytoremediation using advanced analytical techniques are essential for designing phytoremediation technologies with improved, predictable remedial success. Hence, more efforts are needed on addressing the molecular level behaviour of arsenic in plants, kinetics of uptake, and transfer of arsenic in plants with flowing waters, remobilisation through decay, possible methylation, and volatilisation.     

Cd(Ⅱ)与As(Ⅴ)在土壤铁氧化物和细菌表面上的共吸附研究

中国南方土壤常常受到镉砷复合污染,镉砷的化学特性截然不同,因此在土壤不同组分表面的化学行为存在显著区别.在南方偏酸性土壤中铁氧化物占固相比例很大,基于此,选取两种典型土壤组分,即铁氧化物(针铁矿)和微生物(蜡状芽孢杆菌Bacillus cereus),通过批吸附实验结合X-射线光电子能谱探究Cd(II)与As(V)的共...     

吸附法处理含砷废水的研究进展

水体砷污染严重威胁着人类健康和生态系统,砷污染防治成为全球性环境问题,含砷水处理受到人们的普遍关注.与其它除砷方法相比较,吸附法具有去除效率高,稳定性好,不产生或很少产生二次污染,吸附剂可重复使用等优点,因而备受青睐.本文简要介绍了吸附法除砷的原理与特点,重点综述了矿物质、活性炭、金属(氢)氧化物、生物吸附剂、离子交换...     

广州市蔬菜地土壤重金属污染状况调查及评价

探讨了广州市蔬菜地土壤重金属污染状况,测定了95份土壤样品中铅、镉、铬、砷、汞的含量水平。土壤中铅、镉、铬、砷、汞的含量分别在6.44～153.10mg/kg、0-0.682mg/kg、5.82～101.60mg/kg、0.04～45.36mg/kg、0.01～O.32mg/kg之间。就污染的普遍性而言,铅污染最为普遍,其次是砷污染;就污染的程度而言,镉污染最严重.其次为砷、汞。对比今昔污染变化.广州市土壤污染治理已取得显著成效,但仍需努力。土壤中镉、砷、汞三种元素的变异系数,特别是镉的变异系数较大,这可能预示着点源性污染的存在。     

High Cu removal from water using water hyacinth fixed on alginate

The occurrence of toxic metals in waters is a major health issue. Polluted waters can be cleaned by biosorption, which uses organisms such as algae, bacteria, fungi and plants that adsorb metals. In particular, water hyacinth—Eichhornia crassipes—is a promising biosorbent. Here we tested novel alginate-immobilised water hyacinth beads for the removal of Cu from aqueous solutions. Results show that successful service and regeneration continuous cycles were performed using a packed-bed, flow-through column of fixed internal diameter 1.2 cm, at room temperature and pH 5.1, with variation in initial metal concentration, bed depth and flow rate. The eluant used was 1 % w/v CaCl₂ acidified at pH 3. A concentration factor of 12 and elution efficiency up to 98 % were observed in five service and regeneration cycles performed. The equilibrium adsorption capacity of Cu remained almost constant at about 29 mg/g. To conclude, we show for the first time that alginate-immobilised water hyacinth beads can uptake and adsorb Cu very efficiently in a continuous-flow mode, hence highlighting their great potential for removal of toxic metals from aquatic environments.     

利用稀土基无机合成材料去除饮用水中砷的研究

本文研制了一种新型除砷吸附剂,即基于稀土金属铈的无机铈铁吸附剂,并对该吸附剂的除砷效果进行了评价．活性氧化铝和新型研制的铈铁吸附剂对Ａｓ(Ⅴ)吸附平衡比较实验结果表明:活性氧化铝除砷的最佳 ｐＨ为 ３．５－５．５,最大吸附量为８６ｍｇ Ａｓ(Ⅴ)·ｇ－１;而铈铁吸附剂的ｐＨ适用范围广,在ｐＨ３－７的范围内具有较高的除砷性能,最大吸附量可达１６．０ｍｇＡｓ(Ⅴ)·ｇ－１,该吸附材料对Ａｓ(Ⅴ)的吸附基本符合Ｆｒｅｕｎｄｌｉｃｈ型等温方程式,硬度、盐度和氟离子不干扰吸附过程,但磷酸根离子干扰材料对Ａｓ(Ⅴ)的吸附、铈铁无机吸附材料在饮水除砷中具有比较大的应用前景．     

Elemental composition of Jamaican foods 1: A survey of five food crop categories

The concentrations of 27 elements in Jamaican food categories consisting of fruit, legumes, leafy and root vegetables and other root crops are reported. The main analytical techniques used were neutron activation analysis and flame and graphite furnace atomic absorption spectrophotometry. The results are compared, where possible, with values from Denmark, the United Kingdom, the United States and Nigeria, and with some regulatory limits. Over 75% of the results for antimony, arsenic, barium, cerium, thorium and uranium were below the respective sample detection limits but even among these, some of the maximum values observed indicate that further examination may be useful for those foods grown in the regions of highest uptake and consumed in large amounts. The other elements reported are bromine, cadmium, calcium, caesium, cerium, chromium, copper, europium, hafnium, iron, lanthanum, lead, magnesium, manganese, phosphorus, potassium, rubidium, scandium, samarium, sodium, strontium, thorium, uranium, and zinc. Many of these elements occur at concentration levels above those reported from the other countries but it seems unlikely that most of these will contribute significantly to public health risk. However, at this stage cadmium clearly appears to be the element of greatest concern in the Jamaican food chain. The observed range of cadmium concentrations suggests that factors such as land selection, coupled perhaps where necessary, with suitably modified agricultural practices, is a feasible way to reduce the cadmium content of certain local foods.     

Chromosome damage in individuals exposed to heavy metals†

Testing the mutagenic activity of environmental pollutants has become an important area of modern environmental science and prophylactic medicine. The most suitable method for short‐term mutagenicity testing on man, at present, are chromosome studies on somatic cells of exposed individuals. Mutation types analyzed by such studies are of high practical relevance as indicator system of genetic damage induced in man under in vivo conditions. A rather large series of such studies has been dedicated to the action of heavy metals on individuals contacted with these metals under therapeutic, ecological or occupational conditions or by intoxication. Lead, cadmium, chromium, nickel, mercury, zinc and other metals as well as their compounds have been under study. Analyses of that kind, of course, are hampered by difficulties with the distinct estimation of the actual load as well as unclear conditions of exposition, e.g. simultaneous exposition to different metals.

Results obtained till now arouse some suspicion of a direct or indirect mutagenic activity in man by certain chromium and platinum compounds, arsenic, mercury, and combinations of lead with other heavy metals (cadmium, zinc, arsenic, antimony, etc.). Life style, above all smoking habits, well may act comutagenic. In most cases, however, mutagenic activity of metals and metal compounds apparently is clearly superposed by their toxic activity. In specific cases, chromosome studies also may contribute to discover sources of ecological exposition and to monitor occupational load by heavy metals.     

Uncommon heavy metals,metalloids and their plant toxicity: a review

Heavy metals still represent a group of dangerous pollutants, to which close attention is paid. Many heavy metals are essential as important constituents of pigments and enzymes, mainly zinc, nickel and copper. However, all metals, especially cadmium, lead, mercury and copper, are toxic at high concentration because of disrupting enzyme functions, replacing essential metals in pigments or producing reactive oxygen species. The toxicity of less common heavy metals and metalloids, such as thallium, arsenic, chromium, antimony, selenium and bismuth, has been investigated. Here, we review the phytotoxicity of thallium, chromium, antimony, selenium, bismuth, and other rare heavy metals and metalloids such as tellurium, germanium, gallium, scandium, gold, platinum group metals (palladium, platinum and rhodium), technetium, tungsten, uranium, thorium, and rare earth elements yttrium and lanthanum, and the 14 lanthanides cerium, dysprosium, erbium, europium, gadolinium, holmium, lutetium, neodymium, promethium, praseodymium, samarium, terbium, thulium and ytterbium.     

Application of magnesite–bentonite clay composite as an alternative technology for removal of arsenic from industrial effluents

This study evaluated the feasibility of integrating amorphous magnesite and bentonite clay (composite) as an alternative technology for removing arsenic from industrial effluents. The removal of arsenic from industrial effluents by using magnesite–bentonite clay composite was carried out in batch mode. The effects of equilibration time, adsorbent dosage, adsorbate concentration, and pH on removal of arsenic were investigated. The experiments demonstrated that ≈100% arsenic removal is optimum at 30 minutes of agitation, 2 g of adsorbent dosage (2 g: 100 mL, S/L ratio), and 20 mg L^?1 of arsenic concentration. The adsorption data fitted well to both Langmuir and Freundlich adsorption models, hence proving monolayer and multilayer adsorption. The kinetic studies revealed that the data fitted better to a pseudo-second-order reaction than to a pseudo-first-order reaction, hence proving chemisorption. At optimized conditions, the composite was able to remove arsenic to below World Health Organization water quality guidelines, hence depicting that the composite is effective and efficient in removing arsenic from contaminated water. Based on that, this comparative study proves that the composite is a promising adsorbent with high adsorption capacity for arsenic and can be a suitable substitute for the conventional treatment methods.     

Retention characteristics of Cu2+, Pb2+, and Zn2+ from aqueous solutions by two types of low lime fly ashes

The technical feasibility of utilization of fly ash as a low-cost adsorbent for the removal of metals from water has been studied. For two types of fly ashes, the retention capacities of copper, lead, and zinc metal ions have been studied. Contact time, initial concentration, and pH have been varied and their effect on retention mechanism has been studied. The dominant mechanisms responsible for retention are found to be precipitation due to the presence of calcium hydroxide, and adsorption due to the presence of silica and alumina oxide surfaces in the fly ash. First-order kinetic plots have revealed that the rate constant increases with increase in the initial concentration and pH. Langmuir adsorption isotherms have been plotted to study the maximum adsorption capacities for metal ions considered under different conditions. X-ray diffraction studies revealed the formation of new peaks corresponding to respective metal ions precipitates under alkaline conditions.     

The influence of sorption material preparation on the removal of metal ions from the aqueous solution

ABSTRACT

Very important in adsorption processes is the preparation of material sorbents and from this reason, the impact of washing agent of raw sorbent was analysed. The adsorption capacity was studied in relation to the function of the equilibrium time, the amount of biosorbent and the initial metal(II) ions concentration. In this research for the sake of comparison, the sorptive properties of out-of-date coffee were compared to coffee washed with different agents (mineral acids and water). The scanning electron microscopy and Fourier transform infrared spectroscopy were used to characterise the biosorbents and to identify the functional groups that participated in metal(II) ions bonding. The obtained results clearly indicate that the out-of-date coffee are effective biosorbent for cadmium(II) and nickel(II) ions from aqueous solution. However, for metal(II) ions removal efficiency could influence sorbent preparation and nickel(II) ions were best adsorbed on coffee washed with water, but cadmium(II) ions on raw biosorbent (out-of-date coffee). The best results of sorption were achieved after the contact time of 30 and 60?min, respectively for cadmium(II) and nickel(II) ions.     

Variability in the chemistry of private drinking water supplies and the impact of domestic treatment systems on water quality

Tap water from 497 properties using private water supplies, in an area of metalliferous and arsenic mineralisation (Cornwall, UK), was measured to assess the extent of compliance with chemical drinking water quality standards, and how this is influenced by householder water treatment decisions. The proportion of analyses exceeding water quality standards were high, with 65 % of tap water samples exceeding one or more chemical standards. The highest exceedances for health-based standards were nitrate (11 %) and arsenic (5 %). Arsenic had a maximum observed concentration of 440 µg/L. Exceedances were also high for pH (47 %), manganese (12 %) and aluminium (7 %), for which standards are set primarily on aesthetic grounds. However, the highest observed concentrations of manganese and aluminium also exceeded relevant health-based guidelines. Significant reductions in concentrations of aluminium, cadmium, copper, lead and/or nickel were found in tap waters where households were successfully treating low-pH groundwaters, and similar adventitious results were found for arsenic and nickel where treatment was installed for iron and/or manganese removal, and successful treatment specifically to decrease tap water arsenic concentrations was observed at two properties where it was installed. However, 31 % of samples where pH treatment was reported had pH < 6.5 (the minimum value in the drinking water regulations), suggesting widespread problems with system maintenance. Other examples of ineffectual treatment are seen in failed responses post-treatment, including for nitrate. This demonstrates that even where the tap waters are considered to be treated, they may still fail one or more drinking water quality standards. We find that the degree of drinking water standard exceedances warrant further work to understand environmental controls and the location of high concentrations. We also found that residents were more willing to accept drinking water with high metal (iron and manganese) concentrations than international guidelines assume. These findings point to the need for regulators to reinforce the guidance on drinking water quality standards to private water supply users, and the benefits to long-term health of complying with these, even in areas where treated mains water is widely available.