EWP高效污水净化器用于重金属污水治理的试验

电池生产过程排放的污水含汞、锌、锰等重金属污染物和COD等有机污染物。该试验通过调节污水的pH值(7.5～8.5),利用进入EWP高效污水净化器的污水自身生成的Zn(OH)₂絮凝沉淀物形成的吸附过滤流化床对污水进行净化。试验结果表明可达到:出水的汞为0.000 92 mg/L,去除率为96.2%;锌去除率为99.1%;锰去除率为55.1%;COD去除率为19.6%;BOD去除率为28.3%。      

壳聚糖双冠醚的合成及其对金属离子的吸附性能研究

将二苯并16－冠－5氯代乙酸酯冠醚分别接枝到西佛碱型壳聚糖冠醚CT－15C和CT－18C上,制备了1,4－壳聚糖双冠醚CT－15CAC和CT－18CAC,经元素分析、FT－IR红外光谱分析和X－射线粉末衍射分析表征了结构。研究了CT－15CAC和CT－18CAC对Pd^2 、Ag^ 、Pt^4 、Au^3 、Cu^2 、Hg^2 的静态吸附性能,并与CT－15C和CT－18C进行了比较。结果表明,这4种吸附剂对贵金属离子如Au^3 、Ag^ 、Pt^4 、Pd^2 都具有较好的吸附性能,并能在Cu^2 和Hg^2 共存的条件下选择吸附Pd^2 ,而且壳聚糖双冠醚CT－15CAC和CT－18CAC比壳聚糖单冠醚CT－15C和CT－18C具有更好的选择性。     

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.     

Lead removal from water using organic acrylic amine fiber (AAF) and inorganic-organic P-AAF, fixed bed filtration and surface-induced precipitation

Granular porous sorbents were normally used for heavy metals removal from water. To search for the new commercial sorbent and treatment strategy, an organic acrylic amine fiber (AAF) and phosphorus loading inorganic-organic AAF (P-AAF) were prepared and used for lead (Pb) removal from water. A new strategy of inorganic-organic coupling technology was proposed for Pb removal, based on the hypothesis of surface-induced precipitation mechanism. The AAF showed a Pb adsorption capacity of 417 mg/g from the Langmuir fitting, while the column filtration technology was further applied to measure the adsorption edge and applications. Effects of different initial Pb concentrations, hydraulic retention time, and co-existing P were considered in the filtration experiments. The presence of 0.8 mg/L P in water significantly improved the Pb breakthrough point from 15,000 to 41,000 bed volumes of water spiked with 85 µg/L Pb, while the P-AAF fixed bed showed better removal of Pb than AAF SEM/EDX and XRD spectra were employed for determining the surface functional groups and the formation of surface-induced precipitation of pyromorphite (Pb₅(PO₄)₃OH) on AAF. This study verified the application of AAF sorbent for Pb removal and the enhanced effect of coating P on AAF, thus improved our fundamental understanding and application of the surface chemistry process of Pb with P.     

土壤中铁氧化物对铅吸附-解吸的影响

选择上海地区广泛分布的水稻土,通过静态吸附平衡试验,比较土壤去除非晶质氧化铁和去除游离氧化铁后对Pb2+的吸附-解吸行为,采用数学模型拟合,探讨3种土壤的最佳拟合方程、最大吸附的理论值和亲和能力,进而研究非晶质氧化铁和游离氧化铁对Pb2+吸附-解吸的影响。结果表明,去除氧化铁后吸附能力和亲和能力均减弱,原土的最大吸附量为29.21 g/kg,非晶质氧化铁的贡献值为3.52 g/kg,游离氧化铁的贡献值为8.32 g/kg。     

Adsorption and desorption of steroid hormones on saline soil

● Organic matter content significantly affected adsorption of E2/EE2 on saline soil. ● EE2 possessed higher competition intensity for adsorption sites than E2. ● The adsorption of E2/EE2 on saline soil was a spontaneous exothermic process. ● Desorption capacity of EE2/E2 accounted for 40%/78% of the total adsorption capacity. Soil organic matter content was the main driving factor affecting adsorption and desorption process of 17β-estradiol (E2) and 17α-ethynylestradiol (EE2) on saline soil. The adsorption and desorption of E2 and EE2 on three saline soils showed the similar behavior that soil with the highest organic content possessed the highest adsorption capacity and the lowest desorption capacity for E2 and EE2. The adsorption capacity of untreated soil samples (with organic matter) was larger than that of soil samples without organic matter. For soil with the largest adsorption capacity, adsorption capacity of E2/EE2 on the untreated soil and soil colloid (with organic matter) respectively reached 0.15/0.30 μg/g and 0.16/0.33 μg/g while the soil and soil colloid without organic matter hardly adsorbed pollutants. The adsorption capacity of E2/EE2 at the initial concentration of 100 μg/L was 25/15 times higher than that at the initial concentration of 5 μg/L. E2 and EE2 had the same adsorption sites on saline soil while EE2 possessed higher competition intensity for adsorption sites than E2. Pseudo-first-order model (R² = 0.995–0.986) and Langmuir model (R² = 0.989–0.999) could better fit the adsorption process of E2 or EE2. The thermodynamic study further showed that the adsorption of E2/EE2 on saline soil was a spontaneous exothermic process. The desorption capacity of EE2/E2 accounted for 40%/78% of the total adsorption capacity to possibly exert potential risk to the groundwater. The variation of the salinity led to the variation of soil organic carbon which subsequently changed the adsorption and desorption behaviors of endocrine disrupting chemicals in coastal saline soil. This study provides a new insight on the interfacial behavior of endocrine disrupting chemicals on saline soil.