我国电子废弃物管理与资源化对策

电子废弃物对人类环境的影响,已成为全球化的问题。通过对发达国家关于电子废弃物管理以及资源化技术的进展回顾,针对我国目前的情况提出相应的对策:制定延伸生产者责任以及有害物质的停用限期的相应法规;建立电子废弃物回收网络体系;通过国家政策和经济的扶持,尽快建立专门处理电子废弃物的机构;加快我国电子废弃物处理技术的步伐,尽快提高现有工艺及设备。     

电子废弃物资源化全生命周期碳减排效益评估——以废弃电冰箱为例

随着电器电子产品的快速消费和流转,我国正面临电子废弃物国内产生量和国外非法进口量迅速增长的现实问题。废弃电器电子产品处理基金政策(简称"基金"政策)推动了我国电子废弃物资源化产业的发展,带来显著的环境效益。通过解析电子废弃物生命周期过程及其关键的碳减排和碳排放环节,提出了电子废弃物资源化全生命周期碳减排效益评估方法,并以废弃电冰箱为例开展了案例研究。结果表明,制冷剂回收所致碳减排量占废弃电冰箱资源化过程全部碳减排量的92.5%;相对于制冷剂的回收,再生材料产出带来的碳减排效益并不显著;拆解处理所消耗电力的生产是资源化过程碳排放的主要来源,所占比例达89.7%;综合来看,单台废弃电冰箱资源化全生命周期的碳减排效益为1 573.17 kg CO2-eq,2013年我国废弃电冰箱在正规处理体系内资源化带来的碳减排总效益为94.86×104t CO2-eq,"基金"政策驱动效应已初步显现。     

电子废物现状分析及管理对策研究

从电子废物对环境的危害出发,分析了国内外电子废物的处理利用现状,提出了中国电子废物管理的对策与建议,即建立和完善电子废物回收治理的政策体系;建立电子产业的研究机构和技术队伍;建立生产单位的责任激励制度;形成宣传监督管理氛围等。     

苏南危险废物集中处理处置的可行性研究

从法律、技术、环境、经济以及社会层面,结合国际流行管理理念,对苏南危险废物处理处置现状进行了全面评估;提出了苏南危险废物综合管理方案以及废物减量化、资源化、收集、运输、处理处置的技术模式;未来危险废物处理厂的选址方法及标准;新建现代化废弃物物化处理厂、焚烧厂以及填埋场的实施方案。     

电子废弃物的环境污染及防治对策

论述了电子废弃物产生污染的主要原因，分析了其来源及危害，并结合回收，处理和清洁生产，提出了预防和控制电子废弃物污染的具体办法。     

中国城市废弃物的处置和利用

本文分别依次评述适合于中国情况,并在一些地方采用的废弃物处理措施。包括废弃物材科的分类;应用有机废弃物制造混合肥料;有机材科的综合利用,例如利用蚯蚓处理废弃物;用树叶繁殖蘑菇;沼气发发酵;危险废弃物焚化等.     

2004年(第二届)上海国际废弃物处理技术与设备展览会

时间 :2 0 0 4年 4月 2 1日— 2 3日　地点 :上海展览中心展览内容●固体废弃物处理技术与设备输送与储存技术与设备 ;分检技术与设备 ;破碎压迫技术与设备 ;焚烧技术与设备 ;切剪打包技术与设备 ;无害化处理技术与设备●液态废弃物处理技术与设备物理法处理技术与设备 ;化学法处理技术与设备 ;生物法处理技术与设备 ;综合处理技术与设备●资源综合利用技术与设备废旧轮胎再利用技术与设备 ;废弃家用电器再利用技术与设备 ;废弃电池再利用技术与设备 ;其他工业、生活废弃物再利用技术与设备●环境保护服务项目废弃物、废水处理的操作 ;分析…     

南朝鲜的废弃物回收

1961年,南朝鲜发布《污物清扫法》,1986年制定废弃物管理法. 1983年,南朝鲜成立了《韩国废弃物学会》,会长是延世大学教授李承务. 南朝鲜环境部对废弃物处理制定的目标:①减少废物数量;②使其再度为资源加以利用;③进行无公害处理.南朝鲜现有垃圾焚烧炉两座,到2001年,预定建成35座焚烧炉,日处理垃圾量达到9230吨.还计划修建3处有害废弃物处理设施,目前其中的1处已经完工,设在南朝鲜京几道(金浦).     

加油站的烃类VOCs污染及其治理技术

加油站因储运轻质油品而产生的烃类VOCs对健康、环境、安全以及油品质量等带来了一系列负面影响.发达国家的常规治理措施主要是进行密闭卸油和密闭发油,对加油站的设备安装、管线布置、运营管理等都有一些具体要求;进入21世纪后美国又提出了强化加油站油气回收处理的观点,相应的技术、设备及法规也都日益健全.国内目前对加油站烃类VOCs污染的治理工作与发达国家相比差距很大,应该尽快从烃类VOCs回收处理的专用膜分离装置入手进行相关研究和产品开发.     

电子垃圾再循环处理

伟城环保工业（无锡）有限公司建成了电子垃圾再循环的处理设施。处理电子垃圾主要是填埋、焚烧或暂时堆积存放的方法，有的在小作坊里提取金属，严重污染环境。新加坡伟城工业公司是全球技术领先的一站式电子废弃物处理服务商，拥有布满全球的客户网络，以电子垃圾为原料，从中提取金、铜等金属，余下的制成建筑材料、玻璃、塑料地板等副产品，最终实现“零埋制”。     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Synthesis and characterization of m- and p-methylbenzyl-mercapturic acids derived from m- and p-xylenes

Chemical synthesis and physical properties of two mercapturic acids suggested as urinary metabolites of m- and p-xylenes ace described. These compounds may be used for the identification and quantivative determination by high-performance liquid chromatography of the corresponding mercapturic acids in urine.     

Levels of PCDDs and PCDFs in products and effluent from the Swedish pulp and paper industry and chloralkali process

Within the Swedish Dioxin Survey various samples from the pulp and paper industry and the chloralkali process have been analyzed by congener specific analytical methods. In addition to the generally discussed “bleaching pattern” of the tetrachlorinated congeners, these samples also contained higher chlorinated congeners like hexa-CDDs, hepta-CDFs, octa-CDD and octa-CDF. Consequently it is recommended that samples from the pulp industry should be analyzed for all PCDDs and PCDFs (tetra- through octa-). Counted as Nordic Toxic Equivalents (NTEQ), the recycled pulp samples had the highest contamination level followed by TMP, unbleached sulfite and bleached softwood and hardwood. In addition to the bleaching process, various chemicals used in the pulping, bleaching and wastewater treatment can contribute to the contamination.     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

Uptake and translocation of metformin, ciprofloxacin and narasin in forage- and crop plants

Transfer of bioactive organic compounds from soil to plants might represent animal and human health risks. Sewage sludge and manure are potential sources for bioactive compounds such as human- and veterinary drugs. In the present study, uptake of the anti-diabetic compound, metformin, the antibiotic agent ciprofloxacin and the anti-coccidial narasin in carrot (Daucuscarota ssp. sativus cvs. Napoli) and barley (Hordeumvulgare) were investigated. The pharmaceuticals were selected in order to cover various chemical properties, in addition to their presence in relevant environmental matrixes. The root concentration factors (RCF) found in the present study were higher than the corresponding leaf concentration factors (LCF) for the three test pharmaceuticals. The uptake of metformin was higher compared with ciprofloxacin and narasin for all plant compartments analyzed. Metformin was studied more explicitly with regard to uptake and translocation in meadow fescue (Festucapratense), three other carrot cultivars (D.carota ssp. sativus cvs. Amager, Rothild and Nutri Red), wheat cereal (Triticumaestivum) and turnip rape seed (Brassicacampestris). Uptake of metformin in meadow fescue was comparable with uptake in the four carrot cultivars (RCF 2-10, LCF approximately 1.5), uptake in wheat cereals were comparable with barley cereals (seed concentration factors, SCF, 0.02-0.04) while the accumulation in turnip rape seeds was as high as 1.5. All three pharmaceuticals produced negative effects on growth and development of carrots when grown in soil concentration of 6-10 mg kg⁻¹ dry weight.     

Sources and distribution of polychlorinated-dibenzo-p-dioxins and -dibenzofurans in soil and sediment from the Yellow Sea region of China and Korea

Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines.     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.