滇池蓝藻快速热解液化制取生物油的初步研究

文章采用实验室规模的固定床反应器作为实验平台,对蓝藻快速热解液化制取生物油的可行性进行了探讨,并对影响液化性能的诸多因素,如热解温度(300～700℃)、载气流量(0～400 mL/min)、原料粒径(d＜0.08 nn,0.15＜d＜0.25 mm,0.25＜d＜0.38 mm,0.38＜d＜3.35 mm,d＞3....     

稀土磁盘水处理方案技术经济比较

文章针对日照钢铁集团公司2150热轧水处理工程浊环水处理方案选择,对传统沉淀过滤法和先进的稀土磁盘法进行了对比和分析,稀土磁盘法在效果、占地、投资和运行维护费用上有较多优势,最终选用该工艺。     

兰州城区大气PM2.5污染特征及来源解析

为探究兰州城区PM_(2.5)的污染特征及其来源,分别在兰州市城关区和西固区设置PM_(2.5)采样点,于2013年10月(非采暖期)和12月(采暖期)采集样品并进行分析,得到了PM_(2.5)及其16种化学组成的质量浓度.结果表明,兰州城区PM_(2.5)污染水平较高,平均质量浓度为129μg·m~(-3).样品无机元素平均质量浓度为:SCaFeAlMgPbZnMnTiCu,其中S、Ca、Fe、Al的质量浓度在1μg·m~(-3)以上,是主要元素组分;样品各无机元素质量浓度表现为采暖期高于非采暖期,城关区高于西固区.样品水溶性离子平均质量浓度为:SO~(2-)_4NO~-_3NH~+_4Cl~-K~+Na~+,其中SO~(2-)_4、NO~-_3、NH~+_4的质量浓度在10μg·m~(-3)以上,是主要离子组分;样品各水溶性离子质量浓度表现为采暖期高于非采暖期,西固区高于城关区.富集因子(EF)分析结果表明,元素Al、Ca、Mg、Ti的EF值均小于1以自然来源为主;元素Cu、Pb、S、Zn的EF值显著大于10,表明这4种元素在PM_(2.5)中高度富集,且主要源于人为活动造成的污染.主成分分析结果表明,交通排放源、生物质燃烧源、土壤源和二次粒子对兰州城区大气PM_(2.5)贡献显著.     

模拟水体硝态氮对黄菖蒲生长及其氮吸收的影响

为了对挺水植物在水环境与水生态修复中的应用提供参考依据,选取黄菖蒲(Iris pseudacorus L.)为对象,通过模拟水培实验,对比研究了6种水体硝态氮质量浓度(10.68、23.88、42.22、63.33、82.92、97.13 mg·L~(-1))下,黄菖蒲地上和地下生物量、根冠比、叶绿素含量、氮累计吸收量以及对硝态氮去除效果的差异,以期明确模拟水体硝态氮质量浓度对黄菖蒲生长及其氮吸收能力的影响.结果显示,首先,不同硝态氮质量浓度对黄菖蒲地上部分(茎叶)生长的影响大于地下部分(根);当硝态氮质量浓度为10.68 mg·L~(-1)时,黄菖蒲的根冠比增加;当硝态氮质量浓度为42.22~97.13 mg·L~(-1)时,黄菖蒲的根冠比减少.其次,黄菖蒲适宜生长的硝态氮质量浓度为23.88~63.33 mg·L~(-1);硝态氮质量浓度低于10.68 mg·L-1或高于82.92mg·L-1时,均会对黄菖蒲的叶绿素合成产生抑制作用.再次,黄菖蒲对氮的累积量随硝态氮质量浓度增加而增加,且地下部分对氮的累积能力优于地上部分;6种浓度下,单株黄菖蒲的氮累计吸收量为10.56~75.43 mg,其地下部分依次为地上部分的7.2、2.3、2.5、2.1、1.6以及1.5倍.此外,黄菖蒲对氮的利用效率与硝态氮质量浓度之间成显著的幂函数关系,且地上部分的氮利用效率高于地下部分.最后,黄菖蒲对硝态氮的去除率随硝态氮质量浓度增加而增加,6种浓度下黄菖蒲对硝态氮的去除率介于94.9%和99.3%之间,且水体中硝态氮质量浓度随时间延续呈指数函数降低.结果表明,黄菖蒲对硝态氮有很好的去除效果,但黄菖蒲的生长及其对氮的吸收与去除效率受水体硝态氮质量浓度影响显著,且地上部分较地下部分更为敏感.     

三峡库区(重庆-宜昌段)沉积物中钒的污染特征及生态风险评价

为全面了解三峡库区(重庆—宜昌段)干支流沉积物中钒的含量水平、空间分布、赋存形态、污染程度,在三峡库区采集水体沉积物样品67个,测定了沉积物中钒的含量及其化学赋存形态,并采用地积累指数法和潜在生态危害指数法进行分析和评价.结果表明:1三峡库区研究区范围内沉积物中钒的含量范围为89.4~175.2 mg·kg-1,平均值为123.7 mg·kg-1,略高于长江沉积物背景值;2库区沉积物中钒的空间分布特征主要呈现库区干流含量大于支流,干流下游沉积物中钒含量高于上游;3沉积物中钒含量的极值点出现在较发达县(区)附近,考虑其来源可能是人为源汇入;4库区沉积物中钒的赋存形态主要以残渣态为主,所占质量分数为80%~89%,并与总量呈现显著正相关关系;5沉积物中钒污染程度较小,潜在环境危害影响较弱.     

Comparison of quartz sand, anthracite, shale and biological ceramsite for adsorptive removal of phosphorus from aqueous solution

The choice of substrates with high phosphorus adsorption capacity is vital for sustainable phosphorus removal from waste water in constructed wetlands. In this study, four substrates were used： quartz sand, anthracite, shale and biological ceramsite. These substrate samples were characterized by X- ray diffractometry and scanning electron microscopy studies for their mineral components （chemical components） and surface characteristics. The dynamic experimental results revealed the following ranking order for total phosphorus （TP） removal efficiency： anthracite 〉 biological ceramsite 〉 shale 〉 quartz sand. The adsorptive removal capacities for TP using anthracite, biological ceramsite, shale and quartz sand were 85.87, 81.44, 59.65, and 55.98 mg/kg, respectively. Phosphorus desorption was also studied to analyze the substrates＇ adsorption efficiency in wastewater treatment as well as the substrates＇ ability to be reused for treatment. It was noted that the removal performance for the different forms of phosphorus was dependent on the nature of the substrate and the adsorption mechanism. A comparative analysis showed that the removal of particulate phosphorus was much easier using shale. Whereas anthracite had the highest soluble reactive phosphorus （SRP） adsorptive capacity, biological ceramsite had the highest dissolved organic phosphorus （DOP） removal capacity. Phosphorus removal by shale and biological ceramsite was mainly through chemical adsorption, precipitation or biological adsorption. On the other hand, phosphorus removal through physical adsorption （electrostatic attraction or ion exchange） was dominant in anthracite and quartz sand.     

Mo-modified Pd/Al2O3 catalysts for benzene catalytic combustion

Mo-modified Pd/Al2O3catalysts were prepared by an impregnation method and tested for the catalytic combustion of benzene. The catalysts were characterized by N2 isothermal adsorption, X-ray diffraction（XRD）, X-ray photoelectron spectroscopy（XPS）, temperatureprogrammed desorption of NH3（NH3-TPD）, H2temperature-programmed reduction（H2-TPR）, and high-angle annular dark-field scanning transmission electron microscopy（HAADF-STEM）. The results showed that the addition of Mo effectively improved the activity and stability of the Pd/Al2O3catalyst by increasing the dispersion of Pd active components, changing the partial oxidation state of palladium and increasing the oxygen species concentration on the surface of catalyst. In the case of the Pd-Mo/Al2O3catalyst,benzene conversion of 90% was obtained at temperatures as low as 190°C, which was 45°C lower than that for similar performance with the Pd/Al2O3catalyst. Moreover, the 1.0% Pd-5% Mo/Al2O3catalyst was more active than the 2.0% Pd/Al2O3catalyst. It was concluded that Pd and Mo have a synergistic effect in benzene catalytic combustion.     

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.     

Efficient dechlorination of chlorinated solvent pollutants under UV irradiation by using the synthesized TiO2 nano-sheets in aqueous phase

Titanium dioxide(TiO2), which is the widely used photo-catalyst, has been synthesized by simple hydrothermal solution containing tetrabutyl titanate and hydrofluoric acid. The synthesized product has been applied to photo-degradation in aqueous phase of chlorinated solvents, namely tetrachloroethene(PCE), trichloroethene(TCE) and 1,1,1-trichloroethane(TCA). The photo-degradation results revealed that the degradation of these harmful chemicals was better in UV/synthesized TiO2 system compared to UV/commercial P25 system and UV only system. The photo-catalytic efficiency of the synthesized TiO2 was 1.4, 1.8 and 3.0 folds higher compared to the commercial P25 for TCA, TCE and PCE degradation, respectively. Moreover, using nitrobenzene(NB) as a probe of hydroxyl radical(.OH), the degradation rate was better over UV/synthesized TiO2, suggesting the high concentration of.OH generated in UV/synthesized TiO2system. In addition,.OH concentration was confirmed by the strong peak displayed in EPR analysis over UV/synthesized TiO2system. The characterization result using XRD and TEM showed that the synthesized TiO2 was in anatase form and consisted of well-defined sheet-shaped structures having a rectangular outline with a thickness of 4 nm, side length of 50 nm and width of 33 nm and a surface 90.3 m2/g. XPS analysis revealed that ≡Ti-F bond was formed on the surface of the synthesized TiO2. The above results on both photocatalytic activity and the surface analysis demonstrated the good applicability of the synthesized TiO2 nano-sheets for the remediation of chlorinated solvent contaminated groundwater.     

浙江省污水污泥处理处置状况的调查

通过对丽水、宁波、衢州、诸暨等浙江省境内十几个地区的污水处理厂的调查发现:目前浙江省内的污水处理工艺中,A2/O、A/O、氧化沟三种工艺占了近50%的份额。而SBR因其方法特点正在受到越来越多的重视。在污泥处理工艺中,填埋占了最大的一部分,有近70%的污水处理厂将产生的污泥进行填埋处理。目前,污泥处理技术单一,需要继续探寻污泥的减量和资源化技术,为日益增多的污泥探寻出路。