菱镁矿浮选尾矿浆液的烟气脱硫性能

以菱镁矿浮选尾矿浆液为烟气脱硫剂,采用湿法烟气脱硫技术,对模拟烟气进行脱硫研究。实验结果表明：在脱硫剂浆液质量分数10%、脱硫剂浆液温度60 ℃、脱硫时间10 min时,脱硫剂浆液的脱硫率为85%;向脱硫剂浆液中添加柠檬酸和乙二酸时均有助于提高脱硫率,当有机酸的浓度3.5 mmol/L时,添加柠檬酸的脱硫剂浆液的脱硫率为96%,添加乙二酸的脱硫剂浆液的脱硫率为90%。     

响应曲面法优化电化学氧化技术处理染料废水

采用IR和XRD等手段对自制磷钼酸铁(FePMo12)杂多酸进行表征,表明杂多阴离子具有Keggin结构。将FePMo12负载于修饰后的分子筛上制备FePMo12/APTES-4A催化剂填充于电化学反应器中,考察电化学氧化体系对酸性大红3R染料废水的脱色效果,其脱色率高于二维电化学反应器。利用Box-Behnken中心组合实验设计及响应面(RSM)分析,以pH值,板间距,槽电压,曝气量为实验因素,建立了以酸性大红3R的脱色率为响应值的二次多项式回归模型。研究表明,当电解时间为60 min时,曝气量0.05 m3/h、pH为2、板间距3.0 cm、槽电压11.0 V,在此条件下色度去除率可达69.4%,模型预测值与实验值能很好地吻合。方差分析结果表明,槽电压和pH、pH和曝气量的交互作用对响应值具有显著性影响。     

Enhanced uptake of heavy metals in municipal solid waste compost by turfgrass following the application of EDTA

Enhancement of multiple heavy metal uptake from municipal solid waste (MSW) compost by Lolium perenne L. in a field experiment was investigated with application of EDTA. EDTA was added in solution at six rates (0–30 mmol kg^???1) after 50 days of plant growth. Two weeks later, plants were harvested for the first crop and then all the turfgrasses were mowed. After another 30 days of growth, EDTA was added again at above six rates to the corresponding sites and the second crop was harvested 2 weeks later. The results showed that EDTA significantly increased heavy metal accumulation in both crops of L. perenne. For the first crop, the concentrations of Mn, Ni, Cd, and Pb in the shoots increased remarkably with increasing EDTA supply, peaked at 25 mmol kg^???1 EDTA, and shoots of 0–5 cm height (shoots from medium surface to 5 cm height) had higher metal concentrations than 5–10 cm and >10 cm shoots. The highest concentration of Mn, Ni, Cd, and Pb was 2.3-, 2.3-, 2.6-, and 3.2-fold, respectively, in 0–5 cm shoots higher than control. For the second crop, the concentrations of Mn, Cu, and Pb in shoots were, in general, less than those in the first crop. However, the second crop was significantly higher (P?< 0.05) than the first crop in dry biomass, so the total amount of metals removed by the second crop was more than the first crop. In addition, EDTA significantly increased the translocation ratios of most heavy metals from roots to shoots. For the first crop, 38% of the total Zn, 51% of Cd, 49% of Pb, 60% Mn, 55% Ni, and 45% Cu taken up by the plant was translocated in the shoots of 0–5 cm height. Turfgrass would have potential for use in remediation of heavy metals in MSW compost or contaminated soils.     

Distribution of heavy metals in agricultural soils near a petrochemical complex in Guangzhou, China

The aim of the study was to investigate influence of an industrialized environment on the accumulation of heavy metals in agricultural soils. Seventy soil samples collected from surface layers (0-20 cm) and horizons of five selected pedons in the vicinity area of petrochemical complex in Guangzhou, China were analyzed for Zn, Cu, Pb, Cd, Hg and As concentrations, the horizontal and vertical variation of these metals were studied and geographic information system (GIS)-based mapping techniques were applied to generate spatial distribution maps. The mean concentrations of these heavy metals in the topsoils did not exceed the maximum allowable concentrations in agricultural soil of China with the exception of Hg. Significant differences between land-use types showed that Cu, Pb, Cd, Hg and As concentrations in topsoils were strongly influenced by agricultural practices and soil management. Within a radius of 1,300 m there were no marked decreasing trends for these element concentrations (except for Zn) with the increase of distance from the complex boundary, which reflected little influence of petroleum air emission on soil heavy metal accumulation. Concentrations of Zn, Cu, Pb, Cd, Hg and As in the five pedons, particularly in cultivated vegetable field and orchard, decreased with soil depth, indicating these elements mainly originated from anthropogenic sources. GIS mapping was a useful tool for evaluating spatial variability of heavy metals in the affected soil. The spatial distribution maps allowed the identification of hot-spot areas with high metal concentration. Effective measures should be taken to avoid or minimize heavy metal further contamination of soils and to remediate the contaminated areas in order to prevent pollutants affecting human health through agricultural products.     

青岛市环境空气中VOCs的污染特征及化学反应活性

利用2012年青岛市挥发性有机物(VOCs)监测数据,系统分析了VOCs的污染特征、来源和化学反应活性。结果表明,青岛市VOCs浓度处于较低水平,且烷烃是VOCs的主要组分,占60%以上。夏、秋季的VOCs浓度高于春、冬季,且9月的浓度高于其他月份,日变化呈现"两峰一谷"趋势,与交通早晚高峰对应。VOCs各组分均表现出周末效应,说明机动车源和工业源的重要影响,优势物种的相关性分析进一步证明了这一点。对比各组分的OH消耗速率,得出烯烃的臭氧生成贡献高于烷烃和芳香烃,控制机动车尾气、溶剂挥发、化石工业等VOCs排放源将有利于降低大气中的臭氧浓度。     

恶臭气体环境污染损害评估方法初探

依据环境保护部《关于开展环境污染损害鉴定评估工作的若干意见》(环发[2011]60号)及附件《环境污染损害数额计算推荐方法(第I版)》和《突发环境事件污染损害评估工作暂行办法》(征求意见稿),以日照市某公司恶臭气体污染事故为例,按照污染事故损害评估技术路线,通过现场调查和实验室监测分析主要污染物,从人身损害、应急处置、调查评估以及污染修复等方面的损害评估进行了初步探索。     

气象要素及前体物对青岛市臭氧浓度变化的影响

在深入探讨2013—2015年青岛市区O_3污染随时间变化特征的基础上,系统分析了不同气象要素对O_3浓度的影响,并研究了前体物对O_3生成的影响及贡献。结果表明:青岛市区O_3第90百分位日最大8 h滑动平均值和超标率均在2014年达到最高值;O_3浓度在5—10月较高,12月至次年1月浓度最低;O_3日变化呈单峰型变化规律,白天浓度高,夜间浓度低。强太阳辐射、高温、相对湿度60%左右、风速4 m/s左右、偏南风等气象条件下易出现高浓度O_3。O_3的生成主要受前体物VOCs控制,且烯烃对O_3生成的贡献远高于烷烃和芳香烃,控制VOCs尤其是烯烃组分的排放可有效降低青岛市区O_3浓度。     

利用废CRT屏玻璃为原料制备泡沫玻璃

以废阴极射线管(CRT)屏玻璃为主要原料,碳黑为起泡剂,采用粉末烧结法制备了低密度保温泡沫玻璃。通过扫描电镜(SEM)、导热系数测定仪等分析手段,研究了起泡剂的用量、发泡温度和发泡时间对泡沫玻璃泡径、密度、热学性能以及机械力学性能的影响。结果表明,在相同烧制工艺条件下,随起泡剂掺加量增加,烧制所得的泡沫玻璃密度成"V"型变化;当其掺加量为0.20%时,泡沫玻璃在密度、孔径分布以及力学性能上均达到最佳。随着发泡温度的提高和发泡时间的延长,密度会逐渐减小,泡沫玻璃的气泡会逐渐增大,以致产生连通现象。当发泡温度为820℃、发泡时间为30min时烧制的泡沫玻璃密度为0.180 g/cm3,导热系数为0.0695 W/(m.K)。     

Catalytic Activity of Biomorphic α-MoO(3) in the Degradation of Methyl Violet Dye

A network of fibers comprising orthorhombic molybdenum trioxide (α-MoO(3)) crystals were synthesized using paper as template via a biomorphic approach. The template was completely removed by annealing the sample at 600°C for 5?min. Monoclinic MoO(3) was formed and consequently converted into orthorhombic α-MoO(3) after prolonged annealing. Three milligrams of the biomorphic α-MoO(3) could degrade up to 90% of a methyl violet aqueous solution with a concentration of 20?mg/L under normal visible light. The size of the α-MoO(3) grains and the porosity of the biomorphic sample affected catalytic performance.     

Comparative study of adsorption of Pb(II) on native garlic peel and mercerized garlic peel

A comparative study using native garlic peel and mercerized garlic peel as adsorbents for the removal of Pb²⁺ has been proposed. Under the optimized pH, contact time, and adsorbent dosage, the adsorption capacity of garlic peel after mercerization was increased 2.1 times and up to 109.05 mg g^?1. The equilibrium sorption data for both garlic peels fitted well with Langmuir adsorption isotherm, and the adsorbent–adsorbate kinetics followed pseudo-second-order model. These both garlic peels were characterized by elemental analysis, Fourier transform infrared spectrometry (FT-IR), and scanning electron microscopy, and the results indicated that mercerized garlic peel offers more little pores acted as adsorption sites than native garlic peel and has lower polymerization and crystalline and more accessible functional hydroxyl groups, which resulted in higher adsorption capacity than native garlic peel. The FT-IR and X-ray photoelectron spectroscopy analyses of both garlic peels before and after loaded with Pb²⁺ further illustrated that lead was adsorbed on the through chelation between Pb²⁺ and O atom existed on the surface of garlic peels. These results described above showed that garlic peel after mercerization can be a more attractive adsorbent due to its faster sorption uptake and higher capacity.