焦化废水处理技术的发展

焦化废水主要来自焦化厂和煤气厂，污染物组成复杂，含有挥发酚、许多难以生物降解的芳香族有机物、多环化合物和氧硫氮等杂环化合物，属较难生化降解的高浓度有机工业废水。因此焦化废水的处理难度大，已引起国内外人士的关注，一直是国内外废水处理领域的一大难题。文章阐述了焦化废水的处理技术发展及其近年来发展的新技术。     

Integrated energy view of wastewater treatment: A potential of electrochemical biodegradation

• Energy is needed to accelerate the biological wastewater treatment. • Electrical energy input in traditional technology is indirect and inefficient. • Direct injection of electricity can be a game changer to maximize energy efficiency. • Microbial electrochemical unit for decentralized wastewater treatment is proposed. It has been more than one century since the activated sludge process was invented. Despite its proven stability and reliability, the energy (especially the electrical energy) use in wastewater treatment should evolve to meet the increasingly urgent demand of energy efficiency. This paper discusses how the energy utilized in conventional biological wastewater treatment can be altered by switching the indirect energy input to a direct electricity injection, which is achieved by the electrode integration providing extra thermodynamic driving force to biodegradation. By using electrodes instead of oxygen as terminal electron acceptors, the electrical energy can be utilized more efficiently, and the key of direct use of electrical energy in biodegradation is the development of highly active electroactive biofilm and the increase of electron transfer between microbes and the electrode. Furthermore, the synergy of different microbial electrochemical units has additional benefit in energy and resource recovery, making wastewater treatment more sustainable.     

驾驶人危险感知能力影响因素及干预方式综述

为探究外部干预对驾驶人危险感知能力的作用效果,梳理不同理论描述驾驶人危险感知过程,并总结驾驶人危险感知行为机制;然后,从危险感知行为要素出发,分析驾驶风格、驾驶经验、交通环境、驾驶状态对危险感知能力的影响;其次,介绍5种危险感知能力干预方式的研究成果,归纳各方式特点;最后,从干预效果持续性、评价指标、迁移效应等方面总结...     

A Highly Efficient Adsorbent Based on Starch-Graphene Oxide Architecture for Scavenging Aqueous Pb(II): Isotherms,Kinetics, Thermodynamics and Interaction Mechanism

Journal of Polymers and the Environment - Heavy metal pollution stems from the modern industry is a severe environmental problem. In this work, a highly efficient adsorbent based on starch-graphene...     

我国文化和旅游产业融合效率的时空动态演化及其驱动机理

采用仁慈型交叉DEA效率模型、冷热点分析、Tobit模型等方法对2010—2019年我国文化产业和旅游产业融合效率的时空动态演化及驱动机理进行了全面探析,结果发现:①2010—2019年我国文化产业和旅游产业融合效率呈波动上升趋势。②研究期内,文化和旅游产业融合效率呈“东部—中部—西部”依次递减,而融合效率增长率呈“东部—西部—中部”依次递减,但融合增长率都不高。③研究期内,文化产业和旅游产业融合效率呈区域差异性和集聚性。④从文化和旅游产业融合效率驱动机制剖析来看,经济发展、居民消费水平、地区城市化水平、信息发达程度、创新能力、政府政策支持力度是我国文化和旅游产业融合效率的驱动因素,促使效率时空动态演化。     

郑州与福州降水同位素特征及水汽来源对比分析

研究基于郑州与福州两地区GNIP(1985—1992年)大气降水同位素资料,对其大气降水同位素的季节变化以及环境因子进行比较分析。结果表明,郑州地区较福州地区季节变化明显,且两地区与温度和降水量均呈现负相关关系;根据两地区大气降水线方程得出,福州地区大气降水线方程斜率和截距大于郑州地区;两地区的d-excess值夏季高,冬季低;福州地区受台风影响,两地区降水量差别较大导致降水量在决定两地区月加权平均d-excess值时,福州地区整体比郑州地区偏大;采用MeteoInfo软件,并利用由美国国家大气研究中心所提供的气象资料,对两地区气团轨迹进行后向模拟,比较分析得出:郑州地区在夏季大部分水汽来自南海,春季、秋季和冬季的水汽均来自北方大陆;福州地区在夏季的水汽全部水汽来自低纬度的海洋,而春季、秋季和冬季的水汽仅有少部份来自北方大陆。     

Influence of extracellular polymeric substances from activated sludge on the aggregation kinetics of silver and silver sulfide nanoparticles

• The NPs aggregation in the electrolyte solution is consistent with the DLVO theory. • In NaNO₃ and low Ca(NO₃)₂, EPS alleviates the NPs aggregation by steric repulsion. • In high Ca(NO₃)₂, EPS accelerates the NPs aggregation by exopolysaccharide bridging. • Ag₂S NPs have stronger stability compared with Cit-Ag NPs in aqueous systems. Extracellular polymeric substances (EPS) in activated sludge from wastewater treatment plants (WWTPs) could affect interactions between nanoparticles and alter their migration behavior. The influence mechanisms of silver nanoparticles (Ag NPs) and silver sulfide nanoparticles (Ag₂S NPs) aggregated by active EPS sludge were studied in monovalent or divalent cation solutions. The aggregation behaviors of the NPs without EPS followed the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. The counterions aggravated the aggregation of both NPs, and the divalent cation had a strong neutralizing effect due to the decrease in electrostatic repulsive force. Through extended DLVO (EDLVO) model analysis, in NaNO₃ and low-concentration Ca(NO₃)₂ (<10 mmol/L) solutions, EPS could alleviate the aggregation behaviors of Cit-Ag NPs and Ag₂S NPs due to the enhancement of steric repulsive forces. At high concentrations of Ca(NO₃)₂ (10‒100 mmol/L), exopolysaccharide macromolecules could promote the aggregation of Cit-Ag NPs and Ag₂S NPs by interparticle bridging. As the final transformation form of Ag NPs in water environments, Ag₂S NPs had better stability, possibly due to their small van der Waals forces and their strong steric repulsive forces. It is essential to elucidate the surface mechanisms between EPS and NPs to understand the different fates of metal-based and metal-sulfide NPs in WWTP systems.     

Mechanistic insight into the biofilm formation and process performance of a passive aeration ditch (PAD) for decentralized wastewater treatment

• A Passive Aeration Ditch was developed to treat decentralized wastewater. • A model was developed to describe the process performance. • A high C/N ratio facilitates microbial growth but nitrification deteriorates. • A high salinity decreases both organic and nitrogen contaminants removal. Decentralized wastewater containing elevated salinity is an emerging threat to the local environment and sanitation in remote coastal communities. Regarding the cost and treatment efficiencies, we propose a passive aeration ditch (PAD) using non-woven polyester fabric as a feasible bubbleless aerator and biofilm carrier for wastewater treatment. Consideration has been first given to PAD’s efficacy in treating saline decentralized wastewater, and then to the impact of chemical oxygen demand-to-nitrogen (C/N) ratio and salinity on biofilm formation. A multispecies model incorporating the salinity effect has been developed to depict the system performance and predict the microbial community. Results showed that the PAD system had great capacity for pollutants removal. The biofilm thickness increased at a higher C/N ratio because of the boost of aerobic heterotrophs and denitrifying bacteria, which consequently improved the COD and total nitrogen removal. However, this led to the deterioration of ammonia removal. Moreover, while a higher salinity benefited the biofilm growth, the contaminant removal efficiencies decreased because the salinity inhibited the activity of aerobic heterotrophs and reduced the abundance of nitrifying bacteria inside the biofilm. Based on the model simulation, feed water with salinity below 2% and C/N ratio in a range of 1 to 3 forms a biofilm that can reach relatively high organic matter and ammonia removal. These findings not only show the feasibility of PAD in treatment of saline decentralized wastewater, but also offer a systematic strategy to predict and optimize the process performance.     

Product identification and toxicity change during oxidation of methotrexate by ferrate and permanganate in water

• Oxidation of methotrexate by high-valent metal-oxo species was first explored. • Fe(VI) presented a higher reactivity to MTX than Mn(VII) at pH 8.0. • Ketonization and cleavage of peptide bond were two initial reaction pathways. • Products of MTX were not genotoxic, neurotoxic, or endocrine-disrupting chemicals. • The less biodegradable products exhibited developmental and acute/chronic toxicity. Accompanying an annual increase in cancer incidence, the global use of anticancer drugs has remarkably increased with their worldwide environmental prevalence and ecological risks. In this study, the oxidation of methotrexate (MTX), a typical anticancer drug with ubiquitous occurrence and multi-endpoint toxicity, by ferrate(VI) (Fe(VI)) and permanganate (Mn(VII))) was investigated in water. Fe(VI) exhibited a higher reactivity with MTX (93.34 M⁻¹ s⁻¹) than Mn(VII) (3.01 M⁻¹ s⁻¹) at pH 8.0. The introduction of Cu(II) and Fe(III) at 1.0 mM improved the removal efficiency of 5.0 μM MTX by 100.0 μM Fe(VI) from 80% to 95% and 100% after 4 min, respectively. Seven oxidized products (OPs) were identified during oxidative treatments, while OP-191 and OP-205 were characterized as specific products for Fe(VI) oxidation. Initial ketonization of the L-glutamic acid moiety and cleavage of the peptide bond of MTX were proposed. Additionally, a multi-endpoint toxicity evaluation indicated no genotoxicity, neurotoxicity, or endocrine-disrupting effects of MTX and its OPs. Particularly, serious developmental toxicity in zebrafish larvae was observed in the treated MTX solutions. Based on the acute and chronic aquatic toxicity prediction, OP-190, OP-192, OP-206, and OP-208 were deemed toxic or very toxic compared to harmful MTX. Furthermore, the reduced biodegradability index from 0.15 (MTX) to −0.5 to −0.2 (OP-192, OP-206, and OP-468) indicated the formation of lower biodegradable OPs. Overall, this study suggests that Fe(VI) and Mn(VII) oxidation are promising treatments for remediating anticancer drug-contaminated water. However, the environmental risks associated with these treatments should be considered in the evaluation of water safety.     

High performance of multi-layered alternating Ni–Fe–P and Co–P films for hydrogen evolution

Judiciously engineering the electrocatalysts is attractive and challenging to exploit materials with high electrocatalytic performance for hydrogen evolution reaction. Herein, we successfully perform the interface engineering by alternately depositing Co–P and Ni–Fe–P films on nickel foam, via facile electroless plating and de-alloying process. This work shows that there is a significant effect of de-alloying process on alloy growth. The electronic structure of layered alloys is improved by interface engineering. The multilayer strategy significantly promotes the charge transfer. Importantly, the Co–P/Ni–Fe–P/NF electrode fabricated by interface engineering exhibits excellent electrocatalytic hydrogen evolution activity with an overpotential of 43.4 mV at 10 mA cm-2 and long-term durability for 72 h in alkaline medium (1 mol L-1 KOH). The innovative strategy of this work may aid further development of commercial electrocatalysts.