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由于重金属在人体内的累积效应会产生潜在的健康危害,使得食品中的重金属脱除与检测技术越来越受到国内外学者的重视。文章对食品中重金属检测方法的原理及特点进行综述,并介绍几种主要的重金属脱除技术(浸泡法、化学法、吸附法、离子交换法等),同时对食品中重金属脱除技术的未来发展进行展望。 相似文献
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食品重金属污染问题屡见不鲜,重金属在人体内积累后,会严重损害人体的神经系统和肝肾功能。如何去除食品重金属污染,已成为当今世界范围内一个重要的食品安全问题。因此,开发食品中重金属脱除技术对于保障食品安全具有重要意义。常见食品中重金属脱除技术根据原理可分为物理处理法、化学浸提法、微生物法和吸附法等。近年来,食品中重金属脱除技术发展较快,尤其是在吸附法中出现了很多高效、绿色和选择性高的吸附材料。本文总结了食品中各类重金属脱除技术,重点介绍各种技术的研究新进展以及其优缺点,为食品中重金属污染物的脱除提供基础参考,同时有助于促进脱除技术的新发展,并为保障食品安全提供新思路。 相似文献
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大米中重金属污染及其脱除技术研究进展 总被引:1,自引:0,他引:1
现代工业的快速发展,致使我国大米重金属污染问题日益严重。针对我国大米的生产和消费情况以及重金属的污染现状,综述了几种行之有效的重金属检测方法,并对目前大米中重金属污染的脱除技术进行了总结和分析,为今后治理大米中的重金属污染指明了研究方向。 相似文献
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Combined removal of chlorinated ethenes and heavy metals by zerovalent iron in batch and continuous flow column systems 总被引:1,自引:0,他引:1
Dries J Bastiaens L Springael D Agathos SN Diels L 《Environmental science & technology》2005,39(21):8460-8465
The combined removal of chlorinated ethenes and heavy metals from a simulated groundwater matrix by zerovalent iron (ZVI) was investigated. In batch, Ni (5-100 mg L(-1)) enhanced trichloroethene (TCE, 10 mg L(-1)) reduction by ZVI (100 g L(-1)) due to catalytic hydrodechlorination by bimetallic Fe0/Ni0. Cr(VI) or Zn (5-100 mg L(-1)) lowered TCE degradation rates by a factor of 2 to 13. Cr(VI) (100 mg L(-1)) in combination with Zn or Ni (50-100 mg L(-1)) inhibited TCE degradation. Addition of 20% H2(g) in the headspace, or of Zn (50-100 mg L(-1)), enhanced TCE removal in the presence of Ni and Cr(VI). Sorption of Zn to ZVI alleviated the Cr(VI) induced inhibition of bimetallic Fe0/Ni0 apparently due to release of protons necessary for TCE hydrodechlorination. In continuous ZVI columns treating tetrachloroethene (PCE, 1-2 mg L(-1)) and TCE (10 mg L(-1)), and a mixture of the metals Cr(VI), Zn(II), and Ni(II) (5 mg (L-1)), the PCE removal efficiency decreased from 100% to 90% in columns operated without heavy metals. The PCE degradation efficiency remained above 99% in columns receiving heavy metals as long as Ni was present. The findings of this study indicate the feasibility and limitations of the combined treatment of mixtures of organic and inorganic pollutants by ZVI. 相似文献
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近些年食品中重金属超标引发很多问题, 严重危害人民群众的生命健康和社会稳定。传统重金属检测方法有原子吸收光谱法, 原子荧光光谱法和X射线荧光光谱法等, 其具有检测灵敏度高, 选择性好, 检测方法成熟等优点, 但是也存在着检测仪器昂贵, 前处理复杂, 检测所需时间长, 不易携带, 不能满足快速、简单、现场测定的实际需要等不足。科研工作者一直在不断探索能够快速, 灵敏, 高效的检测重金属的技术。适配体具有特异性强, 灵敏度高, 稳定性好等优点, 已经成为一种新型识别分子, 被广泛应用于食品中重金属的检测。本文综述了近年来适配体在镉、汞、铅、砷等重金属检测领域的研究, 并对核酸技术在重金属检测方面进行展望。 相似文献
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《食品与发酵工业》2017,(12):262-267
重金属超标会对人体健康产生极大危害,世界各国日渐重视食品中重金属的限量标准,同时对重金属分析检测方法的研究也越来越多。传统的重金属检测方法比较成熟,灵敏度高,但操作繁琐、费用高昂、依赖大型仪器设备以及需要专业技术人员操作等。酶联免疫(enzyme-linked immune sorbent assay,ELISA)法是一种特异性强、灵敏度高的检测方法,并能用于现场快速检测,故得以迅速发展。ELISA法检测重金属主要包括四大关键步骤:样品前处理、人工抗原的合成、特异性抗体的制备、ELISA方法的选择。该文主要综述了ELISA法在检测重金属方面的最新研究成果,并对该检测技术的研究方向进行了展望。 相似文献
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Anna Witek-Krowiak 《Holz als Roh- und Werkstoff》2013,71(2):227-236
In this work the efficiency of applying non-modified beech sawdust for the removal of Cu2+ and Cr3+ heavy metal ions from water solutions was examined. Parameters taken into consideration in the analysis of environment conditions were influence of sorbent concentration, initial concentration of metal ions, temperature effect, presence of additional substances in solution (NaCl and MgCl2 inorganic salts and anionic and cationic surface-active compounds). Results of kinetic experiments were described by two models: pseudo-first-order and pseudo-second-order; equilibrium results were approximated with five non-linear isotherm models. Maximum sorption capacity at a temperature of 20 °C and pH 5.0 was 30.22 mg g?1 for Cu2+ ions and 41.86 mg g?1 for Cr3+ ions. The positive value of the thermodynamic parameter ΔH° indicates the endothermic nature of the process. Application of 0.1 M HCl as the eluent enables effective desorption of precious metals and reuse of sorbent for purifying water solutions of Cu2+ and Cr3+ ions. 相似文献
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Removal of heavy metals from mine waters by natural zeolites 总被引:1,自引:0,他引:1
Wingenfelder U Hansen C Furrer G Schulin R 《Environmental science & technology》2005,39(12):4606-4613
In this study, we investigated the removal of Fe, Pb, Cd, and Zn from synthetic mine waters by a natural zeolite. The emphasis was given to the zeolite's behavior toward a few cations in competition with each other. Pb was removed efficiently from neutral as well as from acidic solutions, whereas the uptake of Zn and Cd decreased with low pH and high iron concentrations. With increasing Ca concentrations in solution, elimination of Zn and Cd became poorer while removal of Pb remained virtually unchanged. The zeolite was stable in acidic solutions. Disintegration was only observed below pH 2.0. Forward- and back-titration of synthetic acidic mine water were carried out in the presence and absence of zeolite to simulate the effects of a pH increase by addition of neutralizing agents and a re-acidification which can be caused by subsequent mixing with acidic water. The pH increase during neutralization causes precipitation of hydrous ferric oxides and decreased dissolved metal concentrations. Zeolite addition further diminished Pb concentrations but did not have an effect on Zn and Cd concentrations in solution. During re-acidification of the solution, remobilization of Pb was weaker in the presence than in the absence of zeolite. No substantial differences were observed for Fe, Cd, and Zn immobilization. The immobilization of the metals during pH increase and the subsequent remobilization caused by re-acidification can be well described by a geochemical equilibrium speciation model that accounts for metal complexation at hydrous ferric oxides, for ion exchange on the zeolite surfaces, as well as for dissolution and precipitation processes. 相似文献
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从汞的分离富集出发,按测定方法分类,对近来国内外有关汞的形态分析方法特别是荧光分析法的研究进展进行了综述。 相似文献
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Humic acid (HA) coated Fe3O4 nanoparticles (Fe3O4/HA) were developed for the removal of toxic Hg(II), Pb(II), Cd(II), and Cu(II) from water. Fe3O4/HA were prepared by a coprecipitation procedure with cheap and environmentally friendly iron salts and HA. TOC and XPS analysis showed the as-prepared Fe3O4/HA contains approximately 11% (w/w) of HA which are fractions abundant in O and N-based functional groups. TEM images and laser particle size analysis revealed the Fe3O4/HA (with approximately 10 nm Fe3O4 cores) aggregated in aqueous suspensions to form aggregates with an average hydrodynamic size of approximately 140 nm. With a saturation magnetization of 79.6 emu/g, the Fe3O4/HA can be simply recovered from water with magnetic separations at low magnetic field gradients within a few minutes. Sorption of the heavy metals to Fe3O4/HA reached equilibrium in less than 15 min, and agreed well to the Langmuir adsorption model with maximum adsorption capacities from 46.3 to 97.7 mg/g. The Fe3O4/HA was stable in tap water, natural waters, and acidic/ basic solutions ranging from 0.1 M HCl to 2 M NaOH with low leaching of Fe (< or = 3.7%) and HA (< or = 5.3%). The Fe3O4/HA was able to remove over 99% of Hg(ll) and Pb(ll) and over 95% of Cu(II) and Cd(II) in natural and tap water at optimized pH. Leaching back of the Fe3O4/HA sorbed heavy metals in water was found to be negligible. 相似文献
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