Removal of metal ions from aqueous solution by chelating polymeric hydrogel

Polysaccharide natural seed coat from the tree Magonia pubescens, in the form of hydrogel was used to remove metals in aqueous solution. Swelling tests indicate that seed coat presents hydrogel behavior, with maximum water absorption of 292 g water/g. Adsorption experiments performed using Na⁺, Mg²⁺, K⁺, Ca²⁺, Cr³⁺, Fe³⁺ and Zn²⁺ demonstrated that the polysaccharide structure has a high capacity to extract these ions from the aqueous solution. Scanning electron microscopy revealed significant morphological changes of the material before and after water contact. Differential scanning calorimetry measurements indicate a signal shift of the water evaporation temperature in the material with adsorbed zinc. X-ray photoelectron spectroscopy analysis combined with theoretical studies by the density functional theory and on Hartree–Fock (HF) level evidence that the metallic ions were adsorbed through coordination with hydroxyl groups of polysaccharide. In the case of Zn²⁺ the lowest HF energy was observed for the tetracoordination mode, where Zn²⁺ is coordinated by two hydroxyl groups and two water molecules.     

Removal of heavy metals by biosorption

Industrialization and urbanization have resulted in increased releases of toxic heavy metals into the natural environment comprising soils, lakes, rivers, groundwaters and oceans. Research on biosorption of heavy metals has led to the identification of a number of microbial biomass types that are extremely effective in bioconcentrating metals. Biosorption is the binding and concentration of adsorbate from aqueous solutions by certain types of inactive and dead microbial biomass. The novel types of biosorbents presently reviewed are grouped under fungal biomass, biomass of non-living, dried brown marine algae, agricultural wastes and residues, composite chitosan biosorbent prepared by coating chitosan, cellulose-based sorbents and bacterial strains. The reports discussed in this review collectively suggest the promise of biosorption as a novel and green bioremediation technique for heavy metal pollutants from contaminated natural waters and wastewaters.     

二氧化锰基纳米材料对重金属离子的去除及机理研究进展

重金属离子对人类健康和环境安全产生了严重威胁,因此重金属废水高效处理成为了环境领域最具挑战性的热点问题之一.二氧化锰(MnO_2)是一种环境友好型金属氧化物,具有来源广泛、成本低廉、形貌多样、晶型丰富、结构稳定、粒径可控等优异的性质,在重金属离子的去除应用上展现出巨大的潜力.近年来,人们利用MnO_2基纳米材料在重金属离子的有效治理方面开展了大量的研究.本文综述了MnO_2基纳米材料在重金属离子环境修复方面取得的研究进展,包括MnO_2的制备和改性方法,MnO_2基纳米材料在水溶液重金属离子去除中的应用及吸附作用机制,并对研究方向进行了总结和展望,旨在为进一步设计合成对重金属离子的吸附去除具有实际应用价值的MnO_2基纳米材料提供参考.     

Removal of hazardous heavy metals from aqueous environment by low-cost adsorption materials

The rapid growth of the human population and industrialization in the world has indirectly increased environmental problems such as water, air and land pollution. Amongst all, heavy metals can be considered as the most problematic pollutants. Numerous efforts have been attempted to minimize the impact of heavy metals. This chapter discusses the recent developments and technical applicability of different treatment methods for heavy metal removal. The adsorption process using various low-cost materials as the potential alternative for heavy metal removal is being highlighted and summarized.     

水溶液重金属离子在蛭石上的动态吸附行为与化学势变

测试了蛭石-水溶液体系中Pb2+、Cd2+、Zn2+离子的等温动态吸附曲线.实验结果表明蛭石具有较强的去除水溶液中Pb2+、Cd2+、Zn2+离子的能力.基于等温条件下物理化学反应组分的标准化学势为常数的原理,建立了反应体系的动态化学势变方程,为分析离子吸附机理和发展离子吸附技术提供了理论依据与实用方法.测试离子化学势的动态变化证明离子吸附反应遵循电化学势作用定律.     

溶液中多种金属离子共存对毛木耳生物吸附能力的影响

用毛木耳(Auricularia polytricha)菌丝体的死细胞作为生物吸附剂吸附溶液中的Cd 2+、Cu 2+和Pb 2+.用原子吸收分光光度计测定吸附前后溶液金属离子的变化,研究了溶液中两种离子共存对毛木耳吸附能力的影响.结果表明:溶液中Pb2+的存在抑制了毛木耳对Cd2+的吸附,是负向干扰;Cd2+的存在促进了毛木耳对pb2+的吸附,是正向干扰;Cu2+的存在促进了毛木耳对pb2+的吸附,是正向干扰;Pb2+的存在抑制了毛木耳对Cu2+的吸附,是负向干扰;Cd2+对Cu2+的影响作用不如Cu2+对Cd2+的影响明显.实验结果为毛木耳作为重金属污染废水的处理材料提供理论依据.     

Comparative diversity and heavy metal biosorption of myxomycetes from forest patches on ultramafic and volcanic soils

Ultramafic and volcanic soils are exploited for industrial activities such as mining due to their high metal content, thus it is important that species in these areas are documented before irreversible environmental damage sets in. In this study, aerial and ground leaf litter, dead vines and twigs from six forest patches on volcanic and ultramafic soils in the provinces of Bataan, Pangasinan and Zambales in the Philippines were cultured in moist chambers (MC) and assessed for myxomycete diversity. From the 77% positive MC for myxomycetes, a total of 40 species from 14 genera were identified. Despite the higher heavy metal content, forest patches on ultramafic soils had greater species diversity as compared to volcanic soils. In this study, 10 species were abundant in both forest patches, namely Arcyria cinerea, Diachea leucopodia, Diderma effusum, D. hemisphaericum, Didymium ochroideum, Perichaena chrysosperma, P. corticalis, P. depressa, P. dictyonema and Physarum melleum. Selected myxomycetes tested for Cr and Mn content had equal or higher heavy metal levels than that of their leaf substrate. The study hypothesised that the presence of Mn⁷⁺ in fruiting bodies of myxomycetes was due to the phagocytosis of food bacteria inhabiting the substrates on the forest soil laden with heavy metal.     

Removal of heavy metals from aqueous solutions using activated carbon prepared from Cicer arietinum

Removal of Cu²⁺, Cd²⁺, Pb²⁺, and Zn²⁺ from aqueous solutions by activated carbon prepared from stems and seed hulls of Cicer arietinum, an agricultural solid waste, has been studied. The influence of various parameters, such as pH, contact time, adsorbent dose, and initial concentration of metal ions on removal was evaluated. The activated carbon was characterized by FT-IR spectroscopy, X-ray diffraction, and elemental analysis. Sorption isotherms were studied using Langmuir and Freundlich isotherm models. All experimental sorption data were fitted to the sorption models using nonlinear least-squares regression. The maximum adsorption capacity values for activated carbon prepared from Cicer arietinum waste for metal ions were 18 mg g^?1 (Cu²⁺), 18 mg g^?1 (Cd²⁺), 20 mg g^?1 (Pb²⁺), and 20 mg g^?1 (Zn²⁺), respectively. The Freundlich isotherm model fit was best, followed by the pseudo-second-order kinetic model. Desorption studies were carried out with dilute hydrochloric acid for quantitative recovery of the metal ions and for regeneration of the adsorbent.     

Removal of textile dyes from aqueous solution using PEG based aqueous biphasic system

Aqueous biphasic systems (ABSs) composed of polyethylene glycol (PEG) and salt have been examined for the removal of textile dyes from textile effluent. The partitioning of four dyes namely Cibacron Scarlet LS 2G, Rhodamine B, Brown ERN and Astacryl Red 3B was investigated. All the dyes studied were found to partition into the upper PEG rich layer. Sodium carbonate was found to be the most efficient salt for extraction of dyes. Sodium sulphate was found to be marginally less efficient. Sodium chloride did not cause partitioning at all. Partitioning occurred at all pH and was almost pH independent. The partitioning of these dyes in larger volume (100?mL) ABS was also demonstrated. Studies using dye bath effluent were also conducted. In all cases very high efficiencies consistently above 98% were obtained.     

Removal of Cu（ll） ions from aqueous solution by activated carbon impregnated with humic acid

Humic acid （HA） was impregnated onto powdered activated carbon to improve its Cu（II） adsorption capability. The optimum pH value for Cu（II） removal was 6. The maximum adsorption capacity of HAimpregnated activated carbon was up to 5.98mg.g-1, which is five times the capacity of virgin activated carbon. The adsorption processes were rapid and accompanied by changes in pH. In using a linear method, it was determined that the equilibrium experimental data were better represented by the Langmuir isotherm than by the Freundlich isotherm. Surface charges and surface functional groups were studied through zeta potential and FTIR measurements to explain the mechanism behind the humicacid modification that enhanced the Cu（II） adsorption capacity of activated carbon.     

Detection and removal of heavy metal ions: a review

Environmental Chemistry Letters - In aqueous systems, heavy metal ions, when present in excess than permissible limits, are dangerous for human beings and aquatic life. Heavy metals cannot be...     

Interaction between peat, humic acid and aqueous metal ions

Analysis of peat samples from four regions of the British Isles indicates that the concentrations of Al, Pb and common transition metals tend, as expected, to be higher in regions subject to industrial pollution, but that the concentrations of the nontransition metals Na, K, Mg, Ca and Zn tend to be higher in regions remote from industrial pollution. Humic acids were extracted from the most polluted and least polluted of the peat samples and some characteristics of these acids were compared with those of two commercial acids. Values for stability constants of complexes formed between humic acids extracted from peat and Cu²⁺, Zn²⁺ or Pb²⁺ have been obtained by an ionexchange equilibrium method. Of the three metal ions examined, Pb²⁺ was found to form the most stable humic acid complexes, followed by Cu²⁺: this order agrees with the findings of Irving and Williams and of Bunzl. Implications to the binding of actinide and other heavy metal ions in aqueous humic acid are discussed.     

磷酸盐改性方解石去除水中磷酸盐研究

使用磷酸盐溶液和方解石之间的反应得到方解石去除水中磷酸盐后的产物,即磷酸盐改性方解石,通过实验对比分析了方解石和磷酸盐改性方解石对水中磷酸盐的去除动力学,并考察了磷酸盐改性方解石去除水中磷酸盐的各种影响因素。磷酸盐改性方解石对水中磷酸盐的去除能力明显优于方解石。当反应时间为2h时,实验条件下磷酸盐改性方解石对水中磷的去除率达到72%,而方解石对磷的去除率仅为35%。当pH为5~7时,磷酸盐改性方解石对水中磷酸盐的去除能力较高;当pH由7增加到10 h,对磷酸盐的去除能力略微下降;当pH由10增加到12 h,对磷酸盐的去除能力急剧下降。磷酸盐改性方解石对水中磷酸盐的单位去除量随初始磷质量浓度的增加而增加。过高的初始磷质量浓度会导致磷酸盐改性方解石对水中磷酸盐的去除率过低。磷酸盐改性方解石对水中磷酸盐的去除能力随反应温度的升高而增加。磷酸盐改性方解石对水中磷酸盐的去除动力学可以较好地采用准二级动力学模型加以描述。水中共存的钙离子有利于磷酸盐改性方解石对磷酸盐的去除,而水中共存的碳酸氢根离子抑制了磷酸盐改性方解石对磷酸盐的去除。磷酸盐改性方解石去除水中磷酸盐的主要机制是磷酸钙沉淀作用。磷酸盐改性方解石不仅会为磷酸钙沉淀反应的异质成核提供核心,促进磷酸钙沉淀的形成,而且当水处于对方解石不饱和状态时会溶解释放出可溶性钙,为磷酸钙沉淀的形成提供钙源。上述结果表明,方解石去除水中磷酸盐后的产物可以被再次用于水中磷酸盐的去除,并且对磷酸盐的去除效果优于原始的方解石。     

基于局域等离子体纳米材料的水环境中重金属离子可视化监测

重金属污染是重要的水污染问题之一.建立快速、灵敏准确的重金属离子监测新方法,对于水环境保护与水质评估具有重要意义.具有局域表面等离子体共振(LSPR)效应的等离子体纳米材料,在可见光波段具有较强的吸收峰.纳米粒子的聚集或分散,能引起肉眼可辨的颜色变化,由此发展出了纳米材料比色检测技术.本文主要综述了基于等离子体纳米粒子的比色技术在水体中重金属离子检测方面的最新进展,指出了重金属可视化监测技术在实际应用中可能面临的问题,并对未来的发展前景进行了展望.     

RETRACTED ARTICLE: Removal of lead and cadmium ions from aqueous solutions using the macroalga Caulerpa racemosa

Sediment bulk parameters and fatty acid biomarkers were used to investigate the relative contribution of major sources of particulate organic matter during upwelling and non-upwelling conditions, at organic enriched sites on the south-eastern Brazilian coast. The degradation state of the organic material and its implications for benthic food webs were also evaluated. Temperature and salinity values indicate the intrusion of the South Atlantic Central Water in spring with a strong influence at station 4S. C:N ratios and fatty acid biomarkers suggest that sedimentary particulate organic matter is mainly autochthonous and originated from phytoplankton, zooplankton and bacteria, with a minor terrestrial contribution. Short-chain saturated fatty acids predominated, indicating the prevalence of partially degraded detritus. An exception was station 4S, where polyunsaturated fatty acids dominated, indicating the input of labile organic matter linked to upwelling of the South Atlantic Central Water. Fatty acid concentrations and the organic carbon content of the sediments suggest that food quantity is not a limiting factor for benthic fauna. Despite the high organic background of the sediments, the sporadic inputs of labile organic matter associated with South Atlantic Central Water intrusions may produce an important impact on benthic fauna and on the biogeochemistry of the sediments.     

Application of Zr(IV) tungstate for removal of metal ions from aqueous solutions

A heteropolyacid Zr(IV) tungstate-based cation exchanger has been synthesized. An amorphous sample, prepared at pH 1.2 and having a Na⁺ ion exchange capacity of 0.92?meq?g^?1, was selected for further studies. Its physicochemical properties were determined using Fourier transform infrared spectrometer, X-ray diffraction, thermogravimetric, and scanning electron studies. To understand the cation exchange behavior of the material, distribution coefficients (K _d) for metal ions in various solvent systems were determined. Some important binary separations of metal ions, namely Mg²⁺–Bi³⁺, Cd²⁺–Bi³⁺, Fe³⁺–Bi³⁺, Th⁴⁺–Bi³⁺, and Fe³⁺–Zn²⁺, were achieved on such columns. The practical utility of these separations was demonstrated by separating Fe³⁺ and Zn²⁺ ions quantitatively in commercial pharmaceutical formulation. The cation exchanger has been successfully applied also for the treatment of industrial wastewater and a synthetic mixture. All the results suggests that Zr(IV) tungstate has excellent potential for the removal of metals from aqueous systems using packed columns of this material.     

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.     

Removal of clofibric acid from aqueous solution by polyethylenimine-modified chitosan beads

Polyethylenimine （PEI）-modified chitosan was prepared and used to remove clofibric acid （CA） from aqueous solution. PEI was chemically grafted on the porous chitosan through a crosslinking reaction, and the effects of PEI concentration and reaction time in the preparation on the adsorption of clofibric acid were optimized. Scanning electron microscopy （SEM） showed that PEI macromolecules were uniformly grafted on the porous chitosan, and the analysis of pore size distribution indicated that more mesopores were formed due to the crosslinking of PEI molecules in the macropores of chitosan. The PEI-modified chitosan had fast adsorption for CA within the initial 5 h, while this adsorbent exhibited an adsorption capacity of 349 mg· g^-1 for CA at pH 5.0 according to the Langmuir fitting, higher than 213 mg· g^-1 on the porous chitosan. The CA adsorption on the PEI- modified chitosan was pH-dependent, and the maximum adsorption was achieved at pH 4.0. Based on the surface charge analysis and comparison of different pharmaceu- ticals adsorption, electrostatic interaction dominated the sorption of CA on the PEI-modified chitosan. The PEI- modified chitosan has a potential application for the removal of some anionic rnicropollutants from water or wastewater.     

Removal of Diazo dye from aqueous phase by algae Spirogyra species

This communication presents a preliminary study conducted to investigate dye (Direct Brown 2‐Diazo) colour removal using viable algae Spirogyra species. The results indicate the ability of algae Spirogyra species to remove dye colour and found to be dependent on the contact time and biomass. Colour removal mechanism by algae Spirogyra species may be attributed to biosorption and/or bioconversion and/or biocoagulation.     

改性海藻酸钠絮凝剂的合成及其对重金属离子的吸附性能

将海藻酸钠用氨基硫脲进行改性,合成了新型絮凝剂.用红外光谱、核磁共振、元素分析等对该絮凝剂进行了表征.并研究了絮凝剂对5种重金属离子(Fe3+、Cu2+、Pb2+、Cd2+、Hg2+)的絮凝性能.结果表明,改性海藻酸钠絮凝剂对污水中不同浓度的重金属离子均有明显的絮凝效果.吸附动力学表明,絮凝过程在很短时间内即可完成,该产物具有处理重金属离子污水的应用前景.