废水中α-氯代环己基苯基甲酮的电化学降解

采用石墨电极对含α-氯代环己基苯基甲酮的氯化清洗水进行电化学降解。结果表明,电化学降解对COD的去除效果非常明显,并且随着电流密度增加,COD的去除效率逐渐升高,电流密度由15 mA/cm2增加至100 mA/cm2, COD的去除率从39.7%升高到72.3%;电化学降解作用下,水样可生化性显著提高,降解2 h后,(BOD5)/(COD)由原水的0.22提高到0.46;电化学降解过程中,COD的降解遵循零级反应动力学方程;此外,还对电化学降解过程中α-氯代环己基苯基甲酮的降解途径进行了推测。     

生态文明建设实现合作治理的条件、主体和路径分析研究

生态文明建设是政府、市场、非政府组织和公民等多元主体合作治理的整体性系统性实践活动,多元主体合作治理的实现依赖于制度环境、组织因素、共同目标和信息沟通等多个关键条件,同时,合作治理需要各主体按照生态文明建设的要求明确和重塑角色定位,进而通过健全多元主体参与生态文明建设法律保障体系,健全生态补偿和生态支出竞争使用机制,建立信息交互制度,寻求多元合作模式,最终实现统筹协调、联动增效的生态文明建设合作治理.     

药品和个人护理用品在固体基底中的检测方法和分布现状

药品和个人护理用品(Pharmaceuticals and personal care products,PPCPs)在环境中广泛存在,威胁生态环境和人类健康,受到越来越多的关注.本文综述了固体基底中PPCPs的检测方法,总结了国内外污泥、土壤、沉积物等基底中PPCPs的污染现状,并对PPCPs的进一步研究进行了展望.结果表明,PPCPs的检测方法朝多样化和趋优化的方向发展.污泥样品中PPCPs种类多、浓度高(μg·kg-1—mg·kg-1),土壤和沉积物中虽然浓度不高,但是总量不可小觑.目前,固体基底中的PPCPs还需要更全面和更广泛的研究.     

活化过一硫酸盐技术降解环境有机污染物的研究进展

高级氧化技术是一种以产生羟基自由基(·OH)和硫酸根自由基(SO₄?·)来降解环境有机污染物的技术. 近年来,通过活化过一硫酸盐(peroxymonosulfate, PMS)而产生SO₄?·的高级氧化技术受到了广泛关注. 与基于·OH的传统高级氧化技术相比,基于SO₄?·的高级氧化技术具有氧化还原电位高、半衰期长、适用pH范围广和对污染物反应快速等优点. 本文从活化PMS方法的特点和性质出发,对目前活化PMS技术降解环境有机污染物的主要方法和活化机理进行了论述,活化方法包括过渡金属活化(均相和非均相)、碳质材料活化、碱性活化、热活化、辐射活化、电解活化等,活化PMS的机制是通过活化方法使其分子结构中的O—O键发生断裂,从而使PMS分解形成SO₄?·或其他的活性物质. 此外,分析了活化PMS降解环境有机污染物的主要影响因素,其中影响均相系统PMS活化的因素包括过渡金属剂量、pH和水中阴离子等,过量的PMS和过渡金属可能成为SO₄?·的抑制剂,pH不仅对氧化剂分解产生自由基起着关键作用,还影响过渡金属种类的形成及其与氧化剂反应的有效性,而水中阴离子会与有机化合物竞争和SO₄?·发生反应. 最后,提出未来研究重点应在开发稳定高效活化PMS的金属氧化物、碳质材料,以及使用多种处理技术协同作用上,同时应加强对活化PMS技术降解有机污染物体系的降解产物和毒性分析的研究.      

Long‐Term Trends of Nutrients and Sediment from the Nontidal Chesapeake Watershed: An Assessment of Progress by River and Season

To assess historical loads of nitrogen (N), phosphorus (P), and suspended sediment (SS) from the nontidal Chesapeake Bay watershed (NTCBW), we analyzed decadal seasonal trends of flow‐normalized loads at the fall‐line of nine major rivers that account for >90% of NTCBW flow. Evaluations of loads by season revealed N, P, and SS load magnitudes have been highest in January‐March and lowest in July‐September, but the temporal trends have followed similar decadal‐scale patterns in all seasons, with notable exceptions. Generally, total N (TN) load has dropped since the late 1980s, but particulate nutrients and SS have risen since the mid‐1990s. The majority of these rises were from Susquehanna River and relate to diminished net trapping at the Conowingo Reservoir. Substantial rises in SS were also observed, however, in other rivers. Moreover, the summed rise in particulate P load from other rivers is of similar magnitude as from Susquehanna. Dissolved nutrient loads have dropped in the upland (Piedmont and above) rivers, but risen in two small rivers in the Coastal Plain affected by lagged groundwater input. In addition, analysis of fractional contributions revealed consistent N trends across the upland watersheds. Finally, total N:total P ratios have declined in most rivers, suggesting the potential for changes in nutrient limitation. Overall, this integrated study of historical data highlights the value of maintaining long‐term monitoring at multiple watershed locations.     

Determination of 4-tert-octylphenol in surface water samples of Jinan in China by solid phase extraction coupled with GC-MS

Octylphenols, considered as xenoestrogens, mainly exist as 4-tert-octylphenol (OP) in aquatic environments. The high stability and accumulation of OP in aquatic systems have caused endocrine disruption. The OP in surface water in Jinan, China was analyzed by gas chromatography-mass spectrometry (GC-MS) coupled with solid phase extraction (SPE). Water samples were extracted by SPE on a cartridge system containing C-18 as sorbent. To increase sensitivity and selectivity, OP was derivatized to 4-tert-octyl-phenoxy silane. With the use of phenanthrene-d10 as internal standard, the detection limit based on signal-to-noise ratio (S/N = 3) was 0.06 ng/mL. The average recovery was from 84.67% to 109.7%. The precision of the method given as the relative standard deviations (RSD) was within the range 6.24%-12.96%. In the target water samples, the concentrations of OP were as follows: 15.88-71.24 ng/L for Jinxiuchuan Reservoir, 3.850-26.68 ng/L for the city moat, 6.930-41.56 ng/L for Daming Lake, 66.03-474.2 ng/L for Xiaoqing River, 14.66-17.72 ng/L for the Yellow River, and 10.60-26.43 ng/L for Queshan Reservoir. The Xiaoqing River was seriously polluted due to the discharge of wastewater from Jinan. Jinxiuchuan Reservoir had a higher concentration of OP compared with the Yellow River and Queshan Reservoir, which is ascribed to the surrounding human activities. These data are reported for the first time, providing strong support for the control of OP pollution in Jinan.     

Propagation characteristics of subaerial landslide-generated impulse waves

Environmental Fluid Mechanics - Subaerial landslide-generated impulse waves were investigated in a rectangular prismatic channel based on the Froude similarity criterion. Landslides were modeled...     

净化烹饪油污微生物菌种的选育

利用正交试验方法优化了净化烹饪油污菌种选育的环境和营养条件 ,即 :油 :2 0mL、NaNO3( 2g L) :4mL、KH2 PO4( 0 .5g L) :3mL、微量元素溶液 (CuSO4·5H2 O 0 .0 3g L ,ZnSO4·7H2 O 0 .1g L ,MnCl2 ·4H2 O 0 .0 5g L) :1mL和温度 3 7℃ ;而且得出氮源是影响菌体增长的最重要因素 ,温度是影响微生物降解的重要因素 ,而微量元素和磷源对菌种培育结果影响较小。在此优化条件下选育出了合适降解烹饪油污的c种子菌液 ,其每天可降解油 2 2mg L以上 ,并鉴定出主要的微生物是嗜水性气单孢菌 (Aeromonashydrophila 4AK4)、黄丝藻属 (Tribonema)和多甲藻属 (Peridinium)等菌体 ;分析了选育过程活性微生物、目标污染物和微生物的代谢产物三者之间的关系 ,发现所选微生物能利用油类物质作为碳源进行生长代谢     

铁炭微电解工艺处理采油废水的研究

随着采油废水产生量的逐渐增大以及排放标准的日益严格,寻找一种经济、高效的处理方法显得十分必要。采用铁炭微电解技术对冀东油田采油废水进行了处理。考察了铁屑粒径、pH值、Fe/C质量比和反应时间对COD去除率的影响并设计了正交实验,结果表明,影响微电解工艺的因素主次关系为:pH>Fe/C质量比>反应时间,在最佳条件pH=5,Fe/C质量比为7∶1,反应时间50 min下,原水COD由170 mg/L降至95.6 mg/L,去除率达43.85%,出水满足国家二级排放标准。     

Sorption of tylosin on clay minerals

The equilibrium sorption of tylosin (TYL) on kaolinite and montmorillonite was measured at different solution pH using batch reactor systems. The results showed that all the sorption isotherms were nonlinear and that the nonlinearity decreased as the solution pH increased for a given clay. At a specific aqueous concentration, the single-point sorption distribution coefficient (K_D) of TYL decreased rapidly as the solution pH increased. A speciation-dependent sorption model that accounted for the contributions of the cationic and neutral forms of TYL fit the data well, suggesting that the sorption may be dominated by both ion exchange and hydrophobic interactions. The isotherm data also fit well to a dual mode model that quantifies the contributions of a site-limiting Langmuir component (ion exchange) and a non-specific linear partitioning component (hydrophobic interactions). X-ray diffraction analyses revealed that the interlayers of montmorillonite were expanded due to the uptake of TYL. TYL molecules likely form a monolayer surface coverage.