钢渣处理技术的环境性能比较

随着钢铁工业的快速发展,大量钢渣弃置堆积,不仅成为环境污染源,而且占用大量的土地。目前钢渣处理技术较多,其中主要的处理方法有冷弃法、热闷法、热泼法、浅盘法、水淬法、风淬法等。本研究采用生命周期评价方法,对主要钢渣处理技术进行评估,定义了生命周期评估边界和清单指标,建立了清单计算模型,得到了不同钢渣处理技术的生命周期清单。为了提高结果的可信性,对模型进行了不确定性分析。结果表明滚筒法和风淬法的环境性能较好,是值得推广的钢渣处理技术。     

Debromination of decabromodiphenyl ether by organo-montmorillonite-supported nanoscale zero-valent iron：Preparation, characterization and influence factors

An organo-montmorillonite-supported nanoscale zero-valent iron material(M-NZVI) was synthesized to degrade decabromodiphenyl ether(BDE-209). The results showed that nanoscale zero-valent iron had good dispersion on organo-montmorillonite and was present as a core-shell structure with a particle size range of nanoscale iron between 30–90 nm, characterized by XRD, SEM, TEM, XRF, ICP-AES, and XPS. The results of the degradation of BDE-209 by M-NZVI showed that the efficiency of M-NZVI in removing BDE-209 was much higher than that of NZVI. The efficiency of M-NZVI in removing BDE-209 decreased as the pH and the initial dissolved oxygen content of the reaction solution increased, but increased as the proportion of water in the reaction solution increased.     

车用燃料环保管理——《2013年中国机动车污染防治年报》（第V部分）

环境保护部日前发布《2013年中国机动车污染防治年报》,公布了2012年全国机动车污染排放状况。本期“研究成果展示”专栏以六篇形式连载。本文刊载关于车用燃料环保管理的内容,以飨读者。该年报指出。2012年,全国实施车用汽油国Ⅲ阶段标准,硫含量不超过150ppm。按照国家强制性标准《车用汽油》（GB17930—2011）要求,自2014年1月1日起,全国实施车用汽油国IV阶段标准,硫含量不超过50ppm。2012年,我国车用柴油生产和销售执行《车用柴油》（GB19147—2009）标准和《普通柴油》（GB252—2011）标准。按照规定,车用柴油硫含量不得超过350ppm,2013年7月1日后普通柴油硫含量将不得超过350ppm。在已发布第四阶段车用汽油标准（硫含量不大于50ppm）的基础上,由国家质检总局、国家标准委尽快发布第四阶段车用柴油标准（硫含量不大于50ppm）,过渡期至2014年底;2013年6月底前发布第五阶段车用柴油标准（硫含量不大于10ppm）,2013年底前发布第五阶段车用汽油标准（硫含量不大于10ppm）,过渡期均至2017年底。加快国内炼油企业升级改造,确保按照汽、柴油标准升级实施时间如期供应合格油品。2012年环境保护部发布的《关于加强储油库、加油站和油罐车油气污染治理工作的通知》指出,按照国务院批复的《重点区域大气污染防治“十二五”规划》要求,列入大气污染防治“重点控制区”的地区,应限时完成加油站、储油库、油罐车的油气回收治理;大气污染严重的地区可根据本地实际,提前完成油气污染治理工作。     

福建沿海地区大气悬浮颗粒物及颗粒态汞的时空分布研究

2010年4月-2011年3月,对福建省厦门至泉州沿海地区大气中悬浮颗粒物（PM10）和颗粒态汞（TPM）进行为期一年的观测,结果表明其大气中PM10和TPM的浓度范围分别为6.4～426.5μg／m3和18.2～3879.4 pg／m3,PM10和TPM平均浓度分别为122.5μg／m3和947.9pg／m3。不同采样点PM10和TPM浓度的季节变化趋势稍有不同,但大致都呈冬高夏低的趋势。PM10和TPM浓度的季节变化趋势主要与气温、逆温层、降雨量等气象条件有关。同时研究分析了TPM的昼夜变化趋势,结果表明TPM浓度在春冬季主要表现为夜间浓度高于日间浓度,夏秋季则为日间浓度高于夜间浓度。     

海水异养硝化-好氧反硝化芽孢杆菌SLWX2的筛选及脱氮特性

从分离自刺参养殖环境的7株候选菌株中筛选出1株具有较强异养硝化和好氧反硝化能力的菌株SLWX_2,通过形态学特征、生理生化特性和16S rRNA基因测序分析鉴定其为花津滩芽孢杆菌(Bacillus hwajinpoensis).该菌株脱氮特性研究结果表明,SLWX_224 h对氨氮、亚硝酸氮和硝酸氮的去除率分别达到100%、99.5%和85.6%;当3种无机氮源同时存在时,菌株优先利用氨氮,再利用NO_2~--N和NO_3~--N,72 h 3种无机氮的质量浓度均降至0.013 mg·L~(-1)以下,表明该菌株能同时进行异养硝化和好氧反硝化完成脱氮;在氨氮负荷500 mg·L~(-1)、亚硝酸氮负荷100 mg·L·~(-1)和硝酸氮负荷200 mg·L~(-1)范围内,该菌的脱氮能力不受明显抑制,对3种形态的氮均有良好去除效果,96 h最多可去除180 mg NH_4~+-N、30 mg NO_2~--N和120 mg NO_3~--N,并且在硝化过程中没有亚硝酸氮积累.该菌株在海水养殖和高盐高氮工业废水的脱氮处理方面具有更大潜力.     

同源地人工湖水体和底泥中有机物组成及有机结构的分析研究

采用XAD-8大孔吸附树脂对水体和底泥中的有机物进行组分分离,并通过傅里叶变换红外光谱(FTIR)、紫外-可见光谱(UV-Vis)和三维荧光光谱(3DEEMs)对自然水体和底泥中的疏水酸(腐殖酸、富里酸)、疏水碱、疏水中性物质和亲水物质进行表征和对比.结果表明,水体中有机物含量:亲水物质富里酸腐殖酸疏水碱疏水中性物质,底泥中有机物的含量为:腐殖酸富里酸亲水物质疏水碱疏水中性物质.根据红外、紫外、三维荧光光谱可知底泥中有机物的芳香程度、不饱和程度及分子量大小略高于水体有机物.根据荧光指数(FI)和自生源指标(BIX)可知,底泥和水体的腐殖酸和富里酸主要来源于陆生动植物和土壤有机质,而其余物质主要源于细菌和藻类活动.     

锚喷粉尘受力及产尘机理分析

通过对锚喷粉尘的受力分析,基于粉尘颗粒的基本性质,运用牛顿运动规律、流体力学的紊流射流、两相流等相关理论,对锚喷产尘原因及运动规律研究,认为锚喷尘源产生的4种方式: 粉尘颗粒自身的特性及二次风流的影响,高速喷射气流带动周围的空气运动所产生的剪切作用,锚喷高速射流内部中团粒间的相互作用以及物料与受喷面的碰撞是影响锚喷产生粉尘的主要原因.     

Generalized models for prediction of pentachlorophenol dissipation dynamics in soils

Dissipation of pentachlorophenol (PCP) in soil was investigated and the chemical relationships with soil properties were addressed. The results indicate that the dissipation of extractable PCP residues can be described using first-order kinetics equations, with a half-dissipation time (T(1/2)) ranging from 6.5 to 173.3d. The sharply different patterns of PCP dissipation in different soils were closely related to soil properties. Correlations of stepwise regression equations obtained were significant at 0.01 probability level between soil parameters and extractable PCP residues (R(2)=0.974**) as well as T(1/2) values (R(2)=0.882**). Using pH together with organic carbon content (OC) and soil particle size distribution, the dissipation dynamics of PCP in soil could be accurately predicted.     

Polychlorinated biphenyls (PCBs) and halogenated flame retardants (HFRs) in multi-matrices from an electronic waste (e-waste) recycling site in Northern China

The present study investigated the occurrence of polychlorinated biphenyls (PCBs) and halogenated flame retardants (HFRs) in soil, water, reed, air and dust samples collected from the e-waste recycling region in Ziya Town, Northern China. The results showed that the concentrations of PCBs reached relative high level in environmental matrices in the study area. HFRs including polybrominated diphenyl ethers (PBDEs), dechlorane plus (DP), allyl 2,4,6-tribromophenyl ether (ATE), tetrabromoethylcyclohexane (TBECH), pentabromotoluene (PBT), pentabromoethylbenzene (PBEB), 2,3-dibromopropyl 2,4,6-tribromophenyl ether (DPTE), 1,2-bis-(2,4,6-tribromophenoxy) ethane (BTBPE) and so on were also widely detected in multi-matrices. Long-range atmospheric transport (LRAT) potentials of non-BDE HFRs were assessed to address the LRAR abilities of these compounds. Analysis of soil–air exchange of PCBs and HFRs showed that soil acted as a secondary source to the atmosphere only for a few low molecular weight compounds, while the direction of the flux of most detected chemicals was from air to soil.