清洁生产审核中物料平衡的难点及应用实例

建立物料平衡是清洁生产审核第3阶段（即“审核”阶段）最核心的工作内容,其目的是为了准确分析物料流失和废物产生的原因,建立物料平衡也是产生清洁生产方案（尤其是中高费方案）最主要的方法之一。本文在介绍清洁生产审核中物料平衡的完整工作步骤的基础上,归纳了几点在实际工作中应用物料平衡遇到的难点及要点,实例介绍了物料平衡、能源平衡和水平衡三种常用平衡,为审核工作者提供些许思路参考。     

通海台磁通门地磁记录仪基线值日变化现象

通过对通海地磁台2009年到2012年地磁记录日变化准确度标定及基线值数据的精度、稳定性和变化形态的分析,结合观测日所产出地磁总强度数据的F-P检验结果,研究基线值随地磁日变化的变化情况。结果表明,通海台M15(FGE磁通门)磁力仪的ZB、GM4磁通门磁力仪的HB与地磁场的日变化具有一定的相关性,存在日变化现象。     

模糊综合评判在崩塌预测中的应用

本文用模糊数学理论建立了崩塌易发性预测模型,模型中通过对崩塌影响因素的分析,选取8种因素作为预测因子,4个等级作为评价集,并引入k次抛物型模糊分布作为隶属函数。之后采用层次分析法求出权重,使用matlab软件检验权重的一致性并计算结果向量,从而实现对崩塌发育影响因素严重性等级综合评判。实例表明:模糊综合评价方法可操作性强、效果较好,可在一般崩塌发育影响因素分析评价中广泛应用。     

Fenton/微波深度处理增塑剂废水

探讨微波功率、活性炭投加量、pH及反应时间等因素对微波处理效果的影响;考察废水pH、Fe2+和H2O2比例、Fe2+离子浓度及处理时间等因素对Fenton处理效果的影响。分别选择最优条件进行Fenton/微波联合处理邻苯二甲酸酯废水实验,COD去除率达98.7%,出水满足国家综合排放标准中一级标准。     

球形棕囊藻与红树林细菌Flavobacterium sp.相互关系的研究

从深圳福田红树林中分离出一株细菌,对球形棕囊藻有溶藻活性,通过形态鉴定为假单胞菌属细菌。将球形棕囊藻、藻过滤液和提取的溶血毒素与细菌共培养,通过荧光显微计数及平板计数研究活细菌数和可培养细菌数,结果表明:当细菌直接与棕囊藻共培养时,细菌很快进入VBNC状态,细菌能够促进棕囊藻溶血毒素的积累。而将细菌置于透析袋中与棕囊藻一起共培养时,棕囊藻对细菌的VBNC状态影响不大,细菌对棕囊藻溶血毒素的积累无影响。对数期、稳定期棕囊藻培养过滤液和溶血毒素均可使细菌很快进入VBNC状态,溶血毒素可能在球形棕囊藻在被牧食及抑制其他竞争者中(化感作用)扮演着重要的角色。     

基于生命周期的产品碳足迹评价与核算分析

近年来,越来越多的企业对其产品进行碳足迹评价,评价方法主要采用产品碳足迹评价标准提供的碳计量方程,如GHG Protocol、ISO14064、PAS 2050、TS Q 0010等。在介绍相关评价标准的基础上,分析了产品碳足迹的评价步骤,最后利用河北盛华化工有限公司生产的PVC产品为例,给出了基于生命周期的B2B模式的产品碳足迹评价的案例。为企业及相关机构开展碳足迹评价提供借鉴作用。     

废弃产品回收处理企业环境绩效评价初探

近年来,废弃产品回收处理行业日益受到政府和社会各界的关注,而回收处理企业是实施回收处理活动的主体,相关法律、法规的出台对回收处理企业提出了更高的要求。本文在概括梳理相关法律、法规的基础上,初步建立了废弃产品回收处理企业环境绩效评价指标体系,为回收处理企业采用先进的技术工艺、降低环境负荷、加强职业健康监护和企业环境管理提供参考,以适应国家政策要求和行业发展的需要。     

Rhodococcus sp. Ns对硝基苯酚的好氧生物降解

通过驯化富集培养,从红树林底泥中分离出6株硝基苯酚降解菌,其中Rhodococcus sp. Ns为对硝基苯酚（PNP）与邻硝基苯酚（ONP）的高效降解菌.在好氧条件下该菌可以耐受小于1.8 mmol/L的PNP,能够利用PNP和ONP为唯一碳源、能源和氮源生长并将其完全矿化.研究了Rhodococcus sp. Ns在不同pH、盐度与浓度范围下,PNP的降解特性并探讨了该菌降解PNP的途径.实验得出该菌在盐度<5‰、 pH>5的条件下能较快生长,1.5 mmol/L的PNP在96h内被完全降解,并检测到至少2种中间产物4-硝基儿茶酚(4-nitrocatechol)和1,2,4-苯三酚 (1,2,4-benzenetriol).红树林底泥中固有的细菌对PNP和ONP具有高效降解作用.     

Compositions and sources of organic acids in fine particles (PM2.5) over the Pearl River Delta region, south China

Organic acids as important constituents of organic aerosols not only influence the aerosols' hygroscopic property, but also enhance the formation of new particles and secondary organic aerosols. This study reported organic acids including C14–C32fatty acids, C4–C9dicarboxylic acids and aromatic acids in PM2.5collected during winter 2009 at six typical urban, suburban and rural sites in the Pearl River Delta region. Averaged concentrations of C14–C32fatty acids, aromatic acids and C4– C9 dicarboxylic acids were 157, 72.5 and 50.7 ng/m3, respectively. They totally accounted for 1.7% of measured organic carbon. C20–C32fatty acids mainly deriving from higher plant wax showed the highest concentration at the upwind rural site with more vegetation around, while C14–C18fatty acids were more abundant at urban and suburban sites, and dicarboxylic acids and aromatic acids except 1,4-phthalic acid peaked at the downwind rural site. Succinic and azelaic acid were the most abundant among C4–C9dicarboxylic acids, and 1,2-phthalic and 1,4-phthalic acid were dominant aromatic acids. Dicarboxylic acids and aromatic acids exhibited significant mutual correlations except for 1,4-phthalic acid, which was probably primarily emitted from combustion of solid wastes containing polyethylene terephthalate plastics. Spatial patterns and correlations with typical source tracers suggested that C14–C32fatty acids were mainly primary while dicarboxylic and aromatic acids were largely secondary. Principal component analysis resolved six sources including biomass burning, natural higher plant wax, two mixed anthropogenic and two secondary sources; further multiple linear regression revealed their contributions to individual organic acids. It turned out that more than 70% of C14–C18fatty acids were attributed to anthropogenic sources, about 50%–85% of the C20–C32fatty acids were attributed to natural sources, 80%–95% of dicarboxylic acids and 1,2-phthalic acid were secondary in contrast with that 81% of 1,4-phthalic acid was primary.     

Ionic composition of submicron particles (PM1.0) during the long-lasting haze period in January 2013 in Wuhan, central China

In January 2013, a long-lasting severe haze episode occurred in Northern and Central China; at its maximum, it covered a land area of approximately 1.4 million km². In Wuhan, the largest city in Central China, this event was the most severe haze episode in the 21st century. Aerosol samples of submicron particles (PM_1.0) were collected during the long-lasting haze episode at an urban site and a suburban site in Wuhan to investigate the ion characteristics of PM_1.0 in this area. The mass concentrations of PM_1.0 and its water-soluble inorganic ions (WSIIs) were almost at the same levels at two sites, which indicates that PM_1.0 pollution occurs on a regional scale in Wuhan. WSIIs (Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺, Cl^-, NO₃^- and SO₄^2-) were the dominant chemical species and constituted up to 48.4% and 47.4% of PM_1.0 at WD and TH, respectively. The concentrations of PM_1.0 and WSIIs on haze days were approximately two times higher than on normal days. The ion balance calculations indicate that the particles were more acidic on haze days than on normal days. The results of the back trajectory analysis imply that the high concentrations of PM_1.0 and its water-soluble inorganic ions may be caused by stagnant weather conditions in Wuhan.