Synthesis and adsorption performance of lead ion-imprinted micro-beads with combination of two functional monomers

Synthesis and high adsorption and selectivity performance of lead ion-imprinted micro-beads with combination of two functional monomers.     

Simultaneous removal of arsenic and antimony from mining wastewater using granular TiO2: Batch and field column studies

Coexisting arsenic (As) and antimony (Sb) in mining wastewater is a common and great concern. On-site simultaneous removal of As and Sb from mining wastewater was achieved by using a reusable granular TiO₂ column in this study. To evaluate the accuracy of the scale-up procedure, As and Sb adsorption from wastewater was studied in both large (600 g TiO₂) and small columns (12 g TiO₂) based on the proportional diffusivity rapid small-scale column tests (PD-RSSCTs) design. The comparable As and Sb breakthrough curves obtained from small and large columns confirmed the accuracy of the PD-RSSCT theory in the design of large-scale columns. Meanwhile, the consistent As and Sb adsorption results from batch and column experiments suggested that TiO₂ adsorption for As and Sb can be predicted from bench-scale tests. Charge distribution multi-site complexation (CD-MUSIC) and one-dimensional transport modeling integrated in the PHREEQC program were performed to study the adsorption behaviors of As and Sb on the TiO₂ surface. Coexisting ions, such as Ca^2 +, Mg^2 +, and Si^4 +, play an important role in As and Sb adsorption, and the breakthrough curves were well simulated after considering the compound ion effects. The results from this study highlight the surface reactions of As and Sb on TiO₂ and provide a practical way for on-site remediation of industrial wastewater.     

Distribution characteristics and indicator significance of Dechloranes in multi-matrices at Ny-Ålesund in the Arctic

In recent years, Dechloranes have beenwidely detected in the environment around the world. However, understanding and knowledge of Dechloranes in remote regions, such as the Arctic, remain lacking. Therefore, the concentrations of 5 Dechloranes in surface seawater, sediment, soil, moss, and dung collected from Ny-Ålesund in the Arctic were measured with the concentrations 93 pg/L, 342, 325, 1.4, and 258 pg/g, respectively, which were much lower than those in Asian and European regions. The mean ratios of anti-Dechlorane Plus (DP) to total DP (f_anti) in seawater, sediment, soil, moss, dung, and atmospheric samples were 0.36, 0.21, 0.18, 0.27, 0.66, and 0.43, respectively. Results suggested that the main source of DP in seawater, sediment, soil, andmosswas long-range atmospheric transport. However, the ratio identified in dung was different, for which the migration behavior of the organism is probably themain source of DP.     

Distribution characteristics and indicator significance of Dechloranes in multi-matrices at Ny-Ålesund in the Arctic

In recent years, Dechloranes have been widely detected in the environment around the world. However, understanding and knowledge of Dechloranes in remote regions, such as the Arctic, remain lacking. Therefore, the concentrations of 5 Dechloranes in surface seawater, sediment, soil, moss, and dung collected from Ny-Ålesund in the Arctic were measured with the concentrations 93 pg/L, 342, 325, 1.4, and 258 pg/g, respectively, which were much lower than those in Asian and European regions. The mean ratios of anti-Dechlorane Plus (DP) to total DP (?_anti) in seawater, sediment, soil, moss, dung, and atmospheric samples were 0.36, 0.21, 0.18, 0.27, 0.66, and 0.43, respectively. Results suggested that the main source of DP in seawater, sediment, soil, and moss was long-range atmospheric transport. However, the ratio identified in dung was different, for which the migration behavior of the organism is probably the main source of DP.     

Changes in distribution patterns of weed species richness in agricultural lands on Qinghai-Tibet Plateau under climate change北大核心CSCD

农田杂草是阻碍农业生产的主要因素之一.明确农田杂草丰富度分布格局对农业生产管理具有重要意义.以青藏高原农田杂草为研究对象,利用物种分布模型探讨基于县域尺度的农田杂草物种丰富度分布格局及其未来(2050s)的变化,利用逐步回归筛选影响物种丰富度的环境因子,基于传统最小二乘法(OLS)和地理加权回归模型(GWR)分析环境因子对农田杂草物种丰富度的影响,并对两种分析方法进行比较.结果显示:(1)分布在青藏高原的农田主要杂草有51科284种,其中59种单子叶杂草、222种双子叶杂草、135种一年生杂草和149种多年生杂草.青藏高原农田杂草物种丰富度呈由西向东递增的变化规律,物种丰富度中心(丰富度值为167-194)主要集中在一江两河、河湟谷地和川西北等地区;(2)全球气候变化背景下,未来(2050s)青藏高原农田杂草物种丰富度整体呈由东南向西北方向增加的趋势,其中SSP1-2.6情境下最多增加43种,SSP5-8.5情境下最多增加49种;(3)GWR模型优于OLS,其结果表明青藏高原农田杂草物种丰富度的主要驱动因子是最冷季平均温、太阳辐射和最干月降水量,上述变量对杂草丰富度的影响存在明显的空间差异性,其中最冷季平均温由南向北逐渐从负向影响转变为正向影响.太阳辐射整体在青藏高原东部边缘等地区对农田杂草丰富度起正向的影响,在藏东南、青藏高原北部边缘等地区起负向的影响.最干月降水量对整个研究区域起负向影响,并表现出影响力由南向北逐步递增的趋势.上述结果表明青藏高原农田杂草物种丰富度调查不足,实际观测到的丰富度值明显低于当前气候下潜在的丰富度值,存在低估现象.当前气候背景下的农田杂草物种丰富度中心分布地区在未来仍是重点监管对象,且未来青藏高原部分地区作物可能面临新的杂草入侵风险.建议未来研究应注重于青藏高原粮食主产区农田杂草群落结构和功能调查、杂草和作物种间关系、耕地尺度上丰富度驱动因子分析等方面,为区域杂草管理和防治提供充分科学依据.(图6表2参53)     

Intervention factors associated with environmental stressors resulting from cross-provincial transfers by coal resource-based enterprises

Environmental Geochemistry and Health - The environmental stressors associated with the cross-provincial transfer of coal resource-based enterprises (CREs) have become a critical concern for the...     

Association of hearing loss with total and cause-specific mortality in US adults

Environmental Science and Pollution Research - We expected to explore the associations of hearing loss and hearing thresholds at different frequencies with total and cause-specific mortality. In...     

Enhanced reductive degradation of carbon tetrachloride by carbon dioxide radical anion-based sodium percarbonate/Fe(II)/formic acid system in aqueous solution

Complete CT degradation was achieved by SPC/Fe(II)/FA system.Formic acid established the reductive circumstance by producing CO₂·^–.CO₂·^– was the dominant active species responsible for CT degradation.CT degradation was favorable in the pH range from 3.0 to 9.0.SPC/Fe(II)/FA system may be suitable for CT remediation in contaminated groundwater.The performance of sodium percarbonate (SPC) activated with ferrous ion (Fe(II)) with the addition of formic acid (FA) to stimulate the degradation of carbon tetrachloride (CT) was investigated. Results showed that CT could be entirely reduced within 15 min in the system at a variety of SPC/Fe(II)/FA/CT molar ratios in experimental level. Scavenging tests indicated that carbon dioxide radical anion (CO2·^–) was the dominant reactive oxygen species responsible for CT degradation. CT degradation rate, to a large extent, increased with increasing dosages of chemical agents and the optimal molar ratio of SPC/Fe(II)/FA/CT was set as 60/60/60/1. The initial concentration of CT can hardly affect the CT removal, while CT degradation was favorable in the pH range of 3.0–9.0, but apparently inhibited at pH 12. Cl^– and HCO₃^– of high concentration showed negative impact on CT removal. Cl^– released from CT was detected and the results confirmed nearly complete mineralization of CT. CT degradation was proposed by reductive C-Cl bond splitting. This study demonstrated that SPC activated with Fe(II) with the addition of FA may be promising technique for CT remediation in contaminated groundwater.     

Chemical composition of the mycelium of Daldinia eschscholtzii北大核心CSCD

To investigate the chemical composition of the fungus Daldinia eschscholtzii, the compounds were separated by silica gel, Sephadex LH-20, and preparative chromatography. Their structures were identified by spectral methods. The MTT method was applied to measure the cytotoxicity of representative components. Eleven compounds were isolated and identified as 3β-hydroxyl-6,22-dien-5α,8α-peroxynitrite (1); ergosterol-9(11)-dehydroperoxide (2); mangiferonic acid (3); ergosta-4,6,8 (14),22-tetraen-3-one (4); (+)-syringaresinol (5); 3,5,3',5'-tetramethoxy-4,4,-diphenol (6); 5-methoxycoumarin (7); 5-hydroxy-2-methyl-4H-chromen-4-one (8); (2R,4R)-3,4-dihydro-5-methoxy-2-methyl-2H-1-benzopyran-4-ol (9); 2,3-dihydro-5-methoxy-2-methylchromen-4-one (10); and 7β-caruilignan C (11), respectively. Compound 4 showed inhibitory activity against H1299, H460, HGC-27, A5491, and MNK-45, with the IC50 value of 25.2 ± 2.9, 32.3 ± 4.2, 29.2 ± 1.2, 33.9 ± 3.7, and 18.0 ± 7.0 μmol/L, respectively. © 2018 Science Press. All rights reserved.     

土壤中三卤甲烷(THMs)前驱物质流出的规律

通过室内模拟淋溶实验,初步探讨了以三卤甲烷生成潜能(THMFP)为指标的土壤三卤甲烷前驱物质的流出规律.结果显示:土壤淋出液中THMFP的浓度与土壤性质特别是土壤中腐殖质含量、组成与卤代活性,模拟雨水的酸度及累积淋溶量等有关.土壤中所含腐殖质的量越大、腐殖质的卤代活性越高且溶解迁移能力越强,则淋出液中THMFP的浓度越大;酸度最低(pH3.0)的模拟雨水淋洗下,淋出液中THMFP的浓度最低;模拟雨水的pH值愈低,土壤THMFP愈易流出;本实验条件下,淋出液中THMFP的浓度随累积淋溶量的增大呈下降趋势.