基于气流轨迹聚类分析方法浅析桂林市酸雨来源

通过对桂林市2009—2013年的酸雨状况及变化趋势分析,结果表明:桂林市酸雨强度及频率从2010年出现峰值后,呈现逐渐下降的趋势;酸雨的季节分布差异明显,冬、春季酸雨频率较高,夏季相对较低;酸雨中的阴离子主要为SO2-4和NO-3,阳离子主要为Ca2+和NH+4。利用后向轨迹和聚类分析方法对桂林市酸雨来源进行气流轨迹模拟分析,结果显示,主要作用气流来自南方地区,其中东南和偏东南方向气流形成的降雨酸性较强,酸雨频率较高。     

直接进样-热脱附-GC-MS快速测定大气细颗粒物中有机示踪物

建立了直接进样-热脱附-GC-MS快速测定细颗粒物中甾烷类和藿烷类有机示踪物的方法。经实验条件优化,13种目标化合物的线性回归方程的相关系数均在0.990以上,空白加标回收率为81.4%~102.3%,实际样品加标回收率为79.1%~112.9%,相对标准偏差小于13.2%。当采样体积为24 m~3时,各目标化合物的检出限为0.008~0.084 ng/m~3,方法灵敏度高。利用该方法测定了北京城区采暖季和非采暖季PM2.5实际样品,结果表明:各目标物均有检出,且采暖季的甾烷类和藿烷类化合物的总量均明显高于非采暖季。该方法无需复杂的前处理和有机溶剂,操作简便快捷,在颗粒物中非极性化合物的快速检测方面具有很大的应用价值。     

耕地保护外部性及其经济补偿研究进展

耕地保护外部性及其经济补偿问题日益成为经济发展现实中的生态治理研究的重要领域,但既有的研究尚缺乏系统性和理论基础。本文综合运用文献资料法、对比分析法,较为系统的梳理了国内外关于耕地价值核算、耕地保护外部性及其经济补偿研究的代表性观点,在此基础上分析了当前的研究不足与未来的研究取向。研究发现:①国内对耕地价值核算的研究多沿袭国外的理论框架,且对于耕地非市场价值的划分缺少一个明晰的分类体系;②耕地资源外部效益的估算方法应区别对待,且缺少不同方法与途径的比较研究;③耕地外部性的经济补偿标准在时空分配方面的研究有待强化;④缺乏对耕地保护的补偿模式与执行效率的研究。进而提出:应充分借鉴国外经验并结合中国国情,实现耕地价值核算理论框架的整合,并基于利益相关者的分析框架进一步加强耕地保护外部性经济补偿体系、补偿标准及其运行机制方面的研究,推进CVM等价值评价方法等在资源开采矿区生态补偿及资源综合成本核算方面的应用研究。     

高温后钢管再生混凝土短柱的理论分析与试验研究

首先进行了高温后钢管再生混凝土轴压短柱的试验研究,在分析试验结果的基础上提出了高温后核心再生混凝土的应力一应变关系模型,模型考虑了再生粗骨料取代率和曾经历的最高温度的影响;然后采用数值方法对高温后钢管再生混凝土轴压短柱的荷栽一变形全过程关系曲线进行了计算分析,数值计算结果得到试验结果的验证;最后利用数值方法系统分析了再生粗骨料取代率、曾经历的最高温度和约束效应系数等参数对高温后钢管再生混凝土短柱轴压强度系数的影响,并提出了相应的简化计算公式,轴压承载力的简化计算结果与试验结果基本吻合。     

二氧化钛/碳纳米管/壳聚糖薄膜的制备及对苯的降解性能

研究了光催化降解挥发性有机化合物过程中催化剂二氧化钛/碳纳米管/壳聚糖薄膜的制备以及该催化剂对苯的光催化性能。首先采用溶胶-凝胶法制备纳米复合材料二氧化钛/碳纳米管,然后利用壳聚糖作为交联剂,制得二氧化钛/碳纳米管/壳聚糖复合材料催化薄膜。通过傅立叶红外光谱(FT-IR)、X射线衍射(XRD)透射电镜扫描(TEM)和紫外-可见光漫反射(UV-Vis)等技术分析了复合材料薄膜的组成、结构、形貌和对光的吸收性能,然后使用该催化剂对室内常见的污染物苯进行降解,并在同样的实验条件下,使用催化剂二氧化钛(P25)/壳聚糖对苯进行降解,对两者催化性能进行对比,结果表明,二氧化钛/碳纳米管/壳聚糖对苯有更强的吸附能力和更高的催化活性。     

耐盐性毒死蜱降解混合菌的构建及其降解特性

为明确蜡状芽孢杆菌(Bacillus cereus)混合菌株对毒死蜱的降解效果,采用正交实验的方法构建混合菌。以混合菌对毒死蜱的降解率和菌株的生长量为依据,利用单一因素实验考察了不同因素对混合菌降解毒死蜱的影响。结果表明:构建的混合菌中三菌株的体积比为1∶1∶3。在含80 mg/L毒死蜱的反应体系中,最适接菌量为8%(V/V),最适pH为7。在实验浓度下,混合菌对毒死蜱的降解符合一级动力学方程。混合菌对盐分有较高的耐受度,当反应液中氯化钠浓度在20～100 g/L之间时,混合菌对80 mg/L毒死蜱的降解率最高达61%。     

Applicability of MIEX®DOC process for organics removal from NOM laden water

The aim of this study was to evaluate applicability of ion exchange process for organics removal from Douro River surface water at the intake of Lever water treatment plant using magnetized ion exchange resin MIEX®. Qualitative analysis of the natural organic matter present in the surface water and prediction of its amenability to removal in conventional coagulation process were assessed. Results obtained in MIEX®DOC process kinetic batch experiments allowed determination of ion exchange efficiency in dissolved organic carbon (DOC), UV absorbing organics, and true color removal. The data were compared with the efficiencies of the conventional unit processes for organics removal at Lever WTP. MIEX®DOC process revealed to be more efficient in DOC removal than conventional treatment achieving the efficiencies in the range of 61–91 %, lowering disinfection by-products formation potential of the water. DOC removal efficiency at Lever WTP depends largely on the raw water quality and ranges from 28 % for water of moderated quality to 89 % of significantly deteriorated quality. In this work, MIEX®DOC process was also used as a reference method for the determination of contribution of anionic fraction to dissolved organic matter and selectivity of the unit processes at Lever WTP for its removal.     

Life cycle and economic assessment of source-separated MSW collection with regard to greenhouse gas emissions: a case study in China

In China, the continuously increasing amount of municipal solid waste (MSW) has resulted in an urgent need for changing the current municipal solid waste management (MSWM) system based on mixed collection. A pilot program focusing on source-separated MSW collection was thus launched (2010) in Hangzhou, China, to lessen the related environmental loads. And greenhouse gas (GHG) emissions (Kyoto Protocol) are singled out in particular. This paper uses life cycle assessment modeling to evaluate the potential environmental improvement with regard to GHG emissions. The pre-existing MSWM system is assessed as baseline, while the source separation scenario is compared internally. Results show that 23 % GHG emissions can be decreased by source-separated collection compared with the base scenario. In addition, the use of composting and anaerobic digestion (AD) is suggested for further optimizing the management of food waste. 260.79, 82.21, and ?86.21 thousand tonnes of GHG emissions are emitted from food waste landfill, composting, and AD, respectively, proving the emission reduction potential brought by advanced food waste treatment technologies. Realizing the fact, a modified MSWM system is proposed by taking AD as food waste substitution option, with additional 44 % GHG emissions saved than current source separation scenario. Moreover, a preliminary economic assessment is implemented. It is demonstrated that both source separation scenarios have a good cost reduction potential than mixed collection, with the proposed new system the most cost-effective one.     

Characterizing the interactions between polycyclic aromatic hydrocarbons and fulvic acids in water

Polycyclic aromatic hydrocarbons (PAHs) are persistent, bioaccumulative, and toxic chemicals and are listed as priority pollutants by the US EPA. Although they are sparsely soluble in water, their solubility can be increased by binding to dissolved organic matter in natural waters, which will further increase their environmental risk as toxic pollutants. In this study, the interaction between PAHs, exemplified by fluorene and anthracene, and fulvic acid (FA) was studied using fluorescence quenching titration method with fluorescence emission spectra, respectively. The association of FA with the mixture of fluorene and anthracene was also evaluated by excitation–emission matrix (EEM) fluorescence spectrometry combined with parallel factor (PARAFAC) analysis. Results demonstrate that EEM fluorescence spectrometry with PARAFAC analysis was sensitive and reliable to determine the binding properties of PAHs with FA in a mixed aqueous solution. The conditional stability constants and binding capacities show that both PAHs bind to FA tightly.