Kinetics of the reactions of soot surface-bound polycyclic aromatic hydrocarbons with the OH radicals

The kinetics of the heterogeneous reaction of OH radicals with 15 polycyclic aromatic hydrocarbons (PAHs) present in laboratory generated simulated kerosene combustion soot was studied at T = 290 K in a low pressure discharge-flow reactor combined with an electron-impact mass spectrometer. The kinetics of soot-bound PAH consumption in reaction with OH were monitored using off-line HPLC measurements of their concentrations in soot samples as a function of time of exposure to OH. Concentration of OH radicals in the gas phase was measured by mass spectrometry. The first-order rate constants measured for the individual PAH at T = 290 K ranged from 0.02 to 0.04 s^?1 and were found to be independent of the OH concentration ([OH] = (0.34–2.5) × 10¹² molecule cm^?3) and of the molecular structure of the PAH. In addition, the uptake coefficient of OH on soot surface and the diffusion coefficient of OH in He were measured to be 0.19 ± 0.03 (calculated with geometric surface area) and (615 ± 80) Torr cm² s^?1, respectively. Comparison of the results on the PAH + OH reaction to those from previous studies carried out on different carbonaceous substrates, indicates probable dependence of the heterogeneous reactivity of PAH toward OH on the substrate nature. Rapid reaction with OH can be an important potential pathway of the atmospheric degradation of non-volatile PAH present mainly in the particulate phase in the atmosphere.     

Fast determination of sulfonamides and their acetylated metabolites from environmental water based on magnetic molecularly imprinted polymers

Group-selective magnetic molecularly imprinted polymers (MMIPs) that can extract four widely used sulfonamide antibiotics and their acetylated metabolites from environmental water were synthesized in this study. The MMIPs with saturation magnetization value of 16.7 emu g^-1 could be separated from the environmental water samples easily by the application of an adscititious magnetic field, reducing the time consumption of pretreatment. The extraction conditions were evaluated, and optimal extraction conditions were as follows: extraction time, 25 min; amount of polymers, 90 mg; washing solvent, 30 % methanol aqueous solution; and elution solvent, methanol–acetic acid (95:5, v/v). The target analytes were detected by liquid chromatography–tandem mass spectrometry, and the detection limits of the method are in the range of 0.38–1.32 ng L^-1. The relative standard deviations of intra- and inter-day are in the range of 1.3–6.8 % and 1.7–9.1 %, respectively. The proposed method is suitable for the analysis of environmental water samples.     

麻黄素工业废水的生物处理实验

定向培养驯化出生物多样性丰富的活性污泥,并从特异环境中分离筛选出嗜纤维微生物菌株,通过生物食物链的共同作用降解麻黄素类高浓度有机工业废水。     

Synthesis of Polyurethane and Characterization of its Composites Based on Alfa Cellulose Fibers

Polyurethane (PU) based on polycaprolactone (PCL) and 4,4′ diphenyl methylene diisocyanate (MDI) was synthesized using a two-step method. The PU obtained was then blended with various amounts of cellulose extracted from alfa stems to prepare composite materials. The influence of cellulose on the thermal and mechanical properties of different composites was demonstrated by means of several characterization techniques such as Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), scanning electron microscopy (SEM)…     

博乐市空气质量时空变化特征分析

以2001—2008年博乐市空气污染物的监测数据和统计年鉴资料为依据,对其平均浓度的时空变化特征进行分析。结果表明:博乐市空气总体良好,博乐市空气污染物的时空变化特征比较明显,SO2、NO2月变化曲线呈"U"字型,且冬春季节重于夏秋季节,这主要是由冬季取暖和不利气象条件造成的。2006年以来,博乐市TSP浓度呈现明显的空间转化特征,文教区的浓度略高于混合区,应引起环保部门的重视。     

NiO/AC催化臭氧氧化去除水中的苯酚

采用低温湿式浸渍法制备了负载氧化镍/活性炭(简称NiO/AC)催化剂。在不同pH、叔丁醇浓度等条件下,对NiO/AC与臭氧联合催化臭氧氧化苯酚的降解效果等进行了研究。用XRD、SEM及BET技术分析了活性炭与催化剂的组成、形貌及结构变化。结果表明,镍以棒状氧化镍的形式负载在活性炭表面,与AC相比,NiO/AC比表面积减少了47.9%。在O3/NiO/AC与苯酚的反应体系中,反应遵循羟基自由基(HO.)机理,苯酚的去除率比单独臭氧氧化提高了29%,且与溶液pH呈正相关。NiO/AC催化性能较稳定,镍离子最大析出浓度仅为7 mg/L,可重复使用。     

沸腾炉大气污染物的生成与排放特征分析

以20台沸腾炉(功率小于等于60 MW)的燃料特性分析数据和大气污染物的排放实测数据为基础,利用统计分析方法,研究了燃烧过程中排放的颗粒物(PM)、SO_2和NO_x初始排放浓度的影响因素,分析了沸腾炉PM、SO_2和NO_x排放现状,探讨了我国中小型沸腾炉PM、SO_2和NO_x排放管理控制的潜力和可行性.实验结果表明:在锅炉运行负荷大于等于80%的条件下,中小型沸腾炉PM的初始排放浓度基本上不受锅炉出力、过量空气系数和燃煤灰分含量的影响;燃煤的硫含量越高,SO_2初始排放浓度越高;过量空气系数越大,燃煤挥发分越低,NO_x初始排放浓度越高.     

Use of ammoniacal nitrogen tolerant microalgae in landfill leachate treatment

Two microalgae, Chlorella pyrenoidosa and Chlamydomonas snowiae, were isolated from a high ammonia leachate pond in Li Keng Landfill, Guangzhou, China. Their growth and nutrient removal rates were determined in a serial dilution of landfill leachate under laboratory conditions, and their growth rates were compared with that of a C. pyrenoidosa strain isolated from a clean river. The results indicated the growth of all three algae was inhibited by high leachate concentrations, and the inhibition appears linked to high ammonia (ammoniacal-N670mgL(-1)). Significant amounts of ammoniacal-N, ortho-P and COD in the leachate were removed by the algae, with a positive correlation between algal growth and nutrient consumption. Not enough data are available to conclude that one strain was less inhibited by ammoniacal nitrogen or more effective at treating it. Phytotoxicity of leachate was reduced after algal growth, as demonstrated by a seed germination experiment with Brassica chinensis. The germination rates in 10%, 30% and 50% concentrations of algal-treated leachate were significantly higher than those in the same concentration but algal-free leachate.     

Characterization of TSP-bound n-alkanes and polycyclic aromatic hydrocarbons at rural and urban sites of Tianjin, China

Total suspended particle (TSP) was collected and analyzed at rural and urban sites in Tianjin, China during the domestic heating season (from 15 November to 15 March) of 2003/4 for n-alkanes and 16 polycyclic aromatic hydrocarbons (PAHs). The normalized distribution of n-alkanes with the peak at C22, C23, C24 or C25 suggested that fossil fuel utilization was the major source of particulate n-alkanes at both sites. PAHs normalized distribution for each sample was similar and the higher molecular weight PAH dominated the profile (around 90%) indicating a stronger combustion source at both sites. Precipitation and wind were the most important meteorological factors influencing TSP and PAHs atmospheric concentrations. In the urban area the emission height had significant influence on PAHs levels at different heights under the relative stable atmospheric conditions. Coal combustion was the major source for TSP-bound PAHs at both sites based on some diagnostic ratios.