Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous silicates hybrid materials

Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water. A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment.     

Remediation of copper polluted red soils with clay materials

Attapulgite and montmorillonite were utilized to remediate heavy metal polluted red soils in Guixi City, Jiangxi Province, China. The e ects of clay minerals on availability, chemical distribution, and biotoxicity of Cu and Zn were evaluated. The results provided a reference for the rational application of clay materials to remediate heavy metal contaminated soils. From the sorption experiment, the maximum adsorbed Cu2+ by attapulgite and montmorillonite was 1501 and 3741 mg/kg, respectively. After polluted red soil was amended with attapulgite or montmorillonite and cultured at 30 and 60 days, soil pH increased significantly compared to the control. An 8% increase in the amount of montmorillonite in soil and 30 days incubation decreased acid exchangeable Cu by 24.7% compared to the control red soil. Acid exchangeable Cu decreased with increasing amounts of attapulgite and montmorillonite, with best remediation e ect reached at a dose of 8%. Results also showed that the Cu poisoning e ect on earthworms was reduced with the addition of attapulgite and montmorillonite. Montmorillonite showed the best e ect, with the addition of a 2% dose the mortality of earthworms decreased from 60% to zero compared to the control. Our results indicated that the bioavailability of Cu in soils was reduced more e ectively with the application of montmorillonite than attapulgite.     

膜接触器在环境治理中的应用研究进展

膜接触器是将膜分离和传统化工单元操作有机结合而成的一种新型高效分离器,可不通过两相的直接接触而实现相间传质.继21世纪初首个工业化实例成功以来,在废水中芳香族化合物脱除、重金属选择吸收、废气中氨、CO2、H2S去除等多个领域的环境治理中,膜接触器技术的研究与应用日益重要.在此基础上,文章对膜蒸馏、膜吸收、膜萃取和膜填料...     

实验室含铅、镉废水的处理方法探究

文章报道了利用一种新型的环境矿物材料-羟基磷灰石处理实验室高浓度铅、镉污水的方法,该方法与《环境水质监测质量保证手册》中的消石灰处理法相比具有去除速度快、经济有效、无二次污染、安全环保等显著优点。本文还采用消石灰处理法对一次处理后的废水的上清液进行二次处理,这样能使实验室含高浓度的铅、镉废水,在处理后达到地表水三级质量标准。     

绿色环保装修

从设计、施工、材料选择方面简单地探讨绿色环保装修。     

适用于废水处理的DSA电极的研究进展

电化学氧化技术因其具有氧化能力强、可控性高、运行费用低及对环境友好的特点,引起了人们极大的关注.处于核心地位的DSA（Dimensionally Stable Anodes）电极是电化学工作者研究的重点.Ti基氧化铅、氧化铱、锡锑氧化物等电极是目前最有研究价值的DSA电极,文章介绍了这些电极的一些最新的研究成果.     

适用于废水处理的DSA电极的研究进展

电化学氧化技术因其具有氧化能力强、可控性高、运行费用低及对环境友好的特点,引起了人们极大的关注。处于核心地位的DSA（Dimensionally Stable Anodes）电极是电化学工作者研究的重点。Ti基氧化铅、氧化铱、锡锑氧化物等电极是目前最有研究价值的DSA电极,文章介绍了这些电极的一些最新的研究成果。     

硅烷偶联剂对油页岩灰渣制备疏水性SiO_2气凝胶介孔材料的影响

以油页岩灰渣制备的水玻璃为原料,采用不同种类的硅烷偶联剂,在常压下制备了多孔疏水SiO2气凝胶。实验结果表明:在常压干燥之前,对湿凝胶进行溶剂交换-表面改性,是获得多孔气凝胶的关键。未加入硅烷偶联剂制备的气凝胶具有微孔结构;不同硅烷偶联剂制备的SiO2气凝胶均为纳米颗粒组成的中孔结构,比表面积800~980 m2/g,密度0.084~0.11 g/m3,最可几孔径9.38~10.10 nm;FT-IR分析结果表明凝胶表面Si-OH已被改性为Si-CH3,表面呈现较强的疏水性,且疏水性HMDZ>TMCS>DMDC。TG-DTA实验结果表明,改性气凝胶的热稳定性都能达到350℃,HMDZ和TMCS的气凝胶具有更高的热稳定性。     

Removal of polycyclic aromatic hydrocarbons from aqueous solution by raw and modified plant residue materials as biosorbents

Removal of polycyclic aromatic hydrocarbons （PAHs）, e.g., naphthalene, acenaphthene, phenanthrene and pyrene, from aqueous solution by raw and modified plant residues was investigated to develop low cost biosorbents for organic pollutant abatement. Bamboo wood, pine wood, pine needles and pine bark were selected as plant residues, and acid hydrolysis was used as an easily modification method. The raw and modified biosorbents were characterized by elemental analysis, Fourier transform infrared spectroscopy and scanning electron microscopy. The sorption isotherms of PAHs to raw biosorbents were apparently linear, and were dominated by a partitioning process. In comparison, the isotherms of the hydrolyzed biosorbents displayed nonlinearity, which was controlled by partitioning and the specific interaction mechanism. The sorpfion kinetic curves of PAHs to the raw and modified plant residues fit well with the pseudo second-order kinetics model. The sorption rates were faster for the raw biosorbents than the corresponding hydrolyzed biosorbents, which was attributed to the latter having more condensed domains （i.e., exposed aromatic core）. By the consumption of the amorphous cellulose component under acid hydrolysis, the sorption capability of the hydrolyzed biosorbents was notably enhanced, i.e., 6-18 fold for phenanthrene, 6-8 fold for naphthalene and pyrene and 5-8 fold for acenaphthene. The sorpfion coefficients （Kd） were negatively correlated with the polarity index [（O＋N）/C], and positively correlated with the aromaticity of the biosorbents. For a given biosorbent, a positive linear correlation between logKoc and logKow for different PAHs was observed. Interestingly, the linear plots of logKoc-logKow were parallel for different biosorbents. These observations suggest that the raw and modified plant residues have great potential as biosorbents to remove PAHs from wastewater.     

Review of the progress in preparing nano Ti02： An important environmental engineering material

TiO2 nanomaterial is promising with its high potential and outstanding performance in photocatalytic environmental applications, such as CO2 conversion, water treatment, and air quality control. For many of these applications, the particle size, crystal structure and phase, porosity, and surface area influence the activity of TiO2 dramatically. TiO2 nanomaterials with special structures and morphologies, such as nanospheres, nanowires, nanotubes, nanorods, and nanoflowers are thus synthesized due to their desired characteristics. With an emphasis on the different morphologies of TiO2 and the influence factors in the synthesis, this review summarizes fourteen TiO2 preparation methods, such as the sol-gel method, solvothermal method, and reverse micelle method. The TiO2 formation mechanisms, the advantages and disadvantages of the preparation methods, and the photocatalytic environmental application examples are proposed as well.