Rapid degradation of carbon tetrachloride by commercial micro-scale zinc powder assisted by citric acid

We developed an effective method for degradation of carbon tetrachloride (CT) in contaminated water. Zinc metal as a reducing agent for CT in aqueous solutions has been previously studied in some detail, but the rapid corrosion of zinc surface usually reduces its efficiency in removing CT. We assumed that citric acid could enhance the degradation of CT by zinc powder due to the elimination of a passivation layer of Zn(II) (hydr)oxides on the surface of zinc powder through chelating of organic ligands with Zn(II) produced from the reaction and keeping the exposure of active sites to targets. Here the influence of citric acid on the decomposing of CT by commercial micro-scale zinc powder was investigated in a pH range of 3.5–7.5 at 25°C in batch experiments. Reaction mixtures were analysed by gas chromatography/headspace analysis, and Cl⁻ concentration was determined by turbidimetry. The results demonstrate that the degradation of CT by zinc metal alone is very weak, but the addition of citric acid can assist zinc powder to decompose CT more completely and rapidly at all pHs. Degradation of CT took place mainly in the first 10 min of reaction, coupled with 75–95% of CT removal. Maximum dechlorination percentage (82.4%) of CT was obtained at pH 5.5. In that case, chloroform and dichloromethane, as main intermediates, were found at low levels during the whole reaction, suggesting that CT may be sequentially and multiply degraded so quickly that methane is yielded before the intermediates can be desorbed and released to aqueous solution. When compared with the current methods of nano-scale zinc and bimetallic systems, the application of commercial micro-scale zinc particles assisted by organic ligands is of environmental significance since it allows decontamination of aqueous chlorinated organic compounds at low cost and with high efficiency.     

Arsenic accumulation by the aquatic fern Azolla: comparison of arsenate uptake, speciation and efflux by A. caroliniana and A. filiculoides

This study investigates As accumulation and tolerance of the aquatic fern Azolla. Fifty strains of Azolla showed a large variation in As accumulation. The highest- and lowest-accumulating ferns among the 50 strains were chosen for further investigations. Azolla caroliniana accumulated two times more As than Azolla filiculoides owing to a higher influx velocity for arsenate. A. filiculoides was more resistant to external arsenate due to a lower uptake. Both strains showed a similar degree of tolerance to internal As. Arsenate and arsenite were the dominant As species in both Azolla strains, with methlyated As species accounting for <5% of the total As. A. filiculoides had a higher proportion of arsenite than A. caroliniana. Both strains effluxed more arsenate than arsenite, and the amount of As efflux was proportional to the amount of As accumulation. The potential of growing Azolla in paddy fields to reduce As transfer from soil and water to rice should be further evaluated.     

Stormwater runoff quality from different surfaces in an urban catchment in Beijing, China

Urban stormwater runoff quality, widely investigated around the world, has been monitored less in Beijing, China, which impedes the municipal government to use best management practices to protect surface water. In this study, rainwater and stormwater runoff samples from roofs, roads, and a lawn on the campus of the Research Center for Eco-Environmental Sciences (RCEES) (Beijing, China) and from a ring road, with heavy traffic, have been sampled and analyzed for 31 storm events from June 2004 to August 2005. Total suspended solids (TSS), chemical oxygen demand (COD), 5-day biochemical oxygen demand (BOD5), total nitrogen, and total phosphorus concentrations in rainwater and runoff ranged over 2 or more orders of magnitude, meaning that the highest concentration of a certain pollutant did not always occur in a certain kind of runoff. Runoff contained significantly higher concentrations of pollutants than rainwater. On the campus of RCEES, TSS and total phosphorus in runoff samples from the lawn and roads were significantly higher than those from roofs, while the COD, BOD5, and total nitrogen concentrations were not significantly different in runoff among surfaces. Compared with runoff from the roads on campus, runoff from the ring road contained more COD and total nitrogen, but less TSS, BOD5, and total phosphorus. All pollutants measured in runoff from roofs on campus and from the ring road showed a peak concentration in starting runoff, which then decreased sharply. The peak concentrations of COD, BOD5, total nitrogen, and total phosphorus in the roof runoff increased with the increase in time of the antecedent dry period. Thus, urban stormwater pollution control, especially for first-flush control, is of great importance for the full use of rainwater and prevention of water pollution.     

CO3O4/介孔分子筛催化剂对苯催化完全氧化的研究

分别以介孔分子筛MCM-41、MCM-48、SBA-15为载体,采用等体积浸渍法制备了氧化钴/介孔分子筛催化剂,利用N2吸附、X射线衍射、程序升温还原等技术对催化剂进行了表征,考察了Co3O4的负载量及载体的孔结构对催化剂完全催化氧化苯的性能的影响.结果表明,Co3O4的负载量为20%时,催化剂的催化活性最好;载体的孔径和催化剂的可还原性能是影响催化活性的主要因素,催化剂活性顺序为Co3O4/SBA-15>Co3O4/MCM-41>Co3O4/MCM-48.     

Low-cost and efficient adsorbent derived from pyrolysis of Jatropha curcas seeds for the removal of Cu2+ from aqueous solutions

Biochar, is a low-cost material that can be used as an alternative adsorbent for the removal of heavy metals. In this study, a low-cost and efficient adsorbent synthesised from Jatropha curcas seeds was used for the uptake of Cu²⁺ from aqueous solutions. The as-prepared adsorbent was characterised by scanning electron microscopy and Brunauer–Emmett–Teller analysis post calcination at 500 °C, its BET surface area and total pore volume were 39.62?m²?g^?1 and 0.049?m³?g^?1, respectively. Subsequently, the effects of initial pH of the solution, contact time, and adsorbent material dosage on the adsorption of Cu²⁺ by the prepared adsorbent were investigated. The as-prepared adsorbent exhibited a high performance, with a maximum adsorption amount of 32.895?mg?g^?1 for Cu²⁺ at pH 5.0 and 25 °C, owing to the presence of ?OH, C=O, C–O, Si-O-Si, and O-Si-O on its surface. The predominant Cu²⁺ adsorption mechanism was assumed to be ion exchange. Notably, the Cu²⁺ adsorption could attain equilibrium within 90?min. In addition, the fact that the Langmuir model was a better fit than the Freundlich model for the isotherm data of Cu²⁺ adsorption by the as-prepared adsorbent suggested that the adsorption of Cu²⁺ was a monolayer adsorption process.     

Synthesis of a three-dimensional network sodium alginate–poly(acrylic acid)/attapulgite hydrogel with good mechanic property and reusability for efficient adsorption of Cu2+ and Pb2+

Environmental Chemistry Letters - Water pollution caused by heavy metals has dramatically impacted ecosystems in recent years. For instance, 45.4% of lakes in China are in the category of moderate...     

壬基酚对多刺裸腹溞连续世代的毒性效应

为探讨典型环境激素壬基酚(nonylphenol,NP)对枝角类浮游动物多刺裸腹溞连续世代的毒性效应,在实验室条件下,暴露连续3个世代(F0、F1、F2)多刺裸腹溞于0.02~0.10 mg·L-1的NP。15 d后测定成体死亡率、首胎繁殖时间、后代数目、成体蜕皮次数以及终点体长。研究结果表明,NP对F0代多刺裸腹溞具有很高的致死率;随着世代的增加,在相同NP质量浓度暴露下,与母代成体的死亡率相比,子代多刺裸腹溞成体的死亡率增高,致死毒性放大;NP对多刺裸腹溞连续3个世代的繁殖力都有显著抑制作用(P0.05),并随着世代递增,NP对子代繁殖力的抑制增强;在NP暴露下,多刺裸腹溞F0首胎繁殖时间明显推迟,NP暴露浓度与延迟程度呈正相关,呈现出剂量-效应关系,首胎繁殖时间延迟的趋势也存在于F1、F2世代中且存在放大效应;但是连续3个世代多刺裸腹溞成体的蜕皮次数都不受NP暴露影响;F0和F1世代多刺裸腹溞终点体长降低,并呈现明显的剂量-效应关系,但与F1相比,F2低浓度处理组受试个体终点体长呈增加趋势。对结果进行分析,认为多刺裸腹溞在NP暴露后的母代DNA或DNA完整性遭到破坏导致子代在相同NP质量浓度暴露下更容易受到NP致死性的影响;NP化合物具有的苯酚结构抑制枝角类体内葡萄糖、硫酸盐与类固醇的结合,从而引起体内荷尔蒙水平异常,最终对诸如生殖等生理行为造成不利影响;多刺裸腹溞成体的蜕皮次数都不受NP暴露影响表明蜕皮激素系统未受到干扰,且NP对生长的影响显然存在蜕皮外的其他作用机制。     

The impact of government incentives and penalties on willingness to recycle plastic waste: An evolutionary game theory perspective

• Punishments increase the participation probability of collectors and recyclers. • Policy-sponsored incentives make collectors and recyclers to participate earlier. • Recyclers are more sensitive to government punishments than collectors. Because governments have introduced policies involving incentives and penalties to promote the recycling of plastic waste, it is important to understand the impact of such incentives and penalties on the willingness of stakeholders to participate. In this study, government is included as a player, alongside waste collectors and recyclers, in a tripartite evolutionary game model of plastic waste recycling. The study explores the evolutionary equilibrium and performs a simulation analysis to elucidate the effect of government incentives and penalties on the willingness of other players to participate in recycling. Three conclusions are drawn from this research. First, an increase in incentives or in penalties increases the probability that collectors and recyclers will participate in the recycling process. Second, policy support incentives encourage collectors and recyclers to participate in plastic waste recycling earlier than subsidy incentives do. Finally, recyclers are more sensitive than collectors to government-imposed penalties.     

Remediation of soil and groundwater contaminated with organic chemicals using stabilized nanoparticles: Lessons from the past two decades

▪ Overviewed evolution and environmental applications of stabilized nanoparticles. ▪ Reviewed theories on particle stabilization for enhanced reactivity/deliverability. ▪ Examined various in situ remediation technologies based on stabilized nanoparticles. ▪ Summarized knowledge on transport of stabilized nanoparticles in porous media. ▪ Identified key knowledge gaps and future research needs on stabilized nanoparticles. Due to improved soil deliverability and high reactivity, stabilized nanoparticles have been studied for nearly two decades for in situ remediation of soil and groundwater contaminated with organic pollutants. While large amounts of bench- and field-scale experimental data have demonstrated the potential of the innovative technology, extensive research results have also unveiled various merits and constraints associated different soil characteristics, types of nanoparticles and particle stabilization techniques. Overall, this work aims to critically overview the fundamental principles on particle stabilization, and the evolution and some recent developments of stabilized nanoparticles for degradation of organic contaminants in soil and groundwater. The specific objectives are to: 1) overview fundamental mechanisms in nanoparticle stabilization; 2) summarize key applications of stabilized nanoparticles for in situ remediation of soil and groundwater contaminated by legacy and emerging organic chemicals; 3) update the latest knowledge on the transport and fate of stabilized nanoparticles; 4) examine the merits and constraints of stabilized nanoparticles in environmental remediation applications; and 5) identify the knowledge gaps and future research needs pertaining to stabilized nanoparticles for remediation of contaminated soil and groundwater. Per instructions of this invited special issue, this review is focused on contributions from our group (one of the pioneers in the subject field), which, however, is supplemented by important relevant works by others. The knowledge gained is expected to further advance the science and technology in the environmental applications of stabilized nanoparticles.     

Spatial-temporal distribution and potential ecological risk assessment of nonylphenol and octylphenol in riverine outlets of Pearl River Delta, China

The aquatic environments of the Pearl River Delta in Southern China are subjected to contamination with various industrial chemicals from local industries. In this paper, the occurrence, seasonal variation and spatial distribution of alkylphenol octylphenol （OP） and nonylphenol （NP） in fiver surface water and sediments in the runoff outlets of the Pearl River Delta were investigated. NP and OP were detected in all water and sediment samples and their mean concentrations in surface water during the dry season ranged from 810 to 3366 ng/L and 85.5 to 581 ng/L, respectively, and those in sediments ranged from 14.2 to 95.2 ng/g dw and 0.4 to 3.0 ng/g dw, respectively. In surface water, much higher concentrations were detected in the dry season than those in the wet season. In sediments, the concentrations in the dry season were also mostly higher. High concentrations of NP and OP were found in Humen outlet, likely due to high levels of domestic and industrial wastewater discharges. An ecological risk assessment with the use of hazard quotient （HQ） was also carried out and the HQvalues ranged from 3.6 × 10^-5 to 35 and 64% of samples gave a HQ 〉 1, indicating that the current levels of NP and OP pose a significant risk to the relevant aquatic organisms in the region.