Ozone facilitated degradation of caffeine using Ce-TiO2 catalyst

The ozone initiated oxidation of 1,3,7-trimethylxanthine (caffeine), commonly found in wastewaters as model compound is reported using cerium (Ce)/titanium dioxide (TiO₂) as catalyst. The effect of pH and loading of ceria on titania were investigated. Effect of reaction conditions on degradation of caffeine based on their pseudo first-order rate constants were compared. The combination of catalyst Ce-TiO₂ and ozone aeration significantly enhanced the degradation of caffeine compared to uncatalysed ozonation. The oxidation of caffeine ensued via the free radical mechanism, through enhanced ozone decomposition into OH radicals. Ce/TiO₂(0.5?wt%) showed good activity in degradation of caffeine at pH 6, in both natural stream and river water samples showing about 60% total organic carbon removal in 2?h ozonation period. Using liquid chromatography-mass spectroscopy, degradation products were analysed. A reaction intermediate and one final product were positively identified. Nano-catalysts with different loadings of Ce on TiO₂ synthesized by sol-gel route were characterized by scanning electron microscope, transmission electron microscopy, BET and powder X-ray diffraction spectrum techniques. The results showed that the material retained a highly ordered mesoporous structure and possessed large surface area.     

磁性Fe_3O_4/石墨烯纳米复合材料催化降解水中17β-雌二醇

利用化学沉淀法制备磁性四氧化三铁/石墨烯(Fe3O4/GE)纳米复合材料,并将其与H2O2构成非均相Fenton体系用于催化降解水中微量的17β-雌二醇(E2),研究了初始p H值,初始H2O2浓度,催化剂用量对E2降解的影响。结果表明,Fe3O4/GE纳米复合材料在无需外加光源的条件下能够有效催化降解E2。在p H 7.0,E2初始浓度为1 mg/L,初始H2O2浓度为15 mmol/L,Fe3O4/GE投加量为15 mg/L的条件下,反应8 h后可去除92.9%的E2。Fe3O4/GE具有便捷的磁分离特性和稳定的催化活性,经过7次循环使用后对E2的降解效率仍保持在91.5%左右。     

PVC/PES-g-PEGMA共混膜的制备及其耐污染性能

首先将聚乙二醇单甲基甲醚酯(PEGMA)接枝到聚醚砜(PES)上得到PES-g-PEGMA,然后利用溶液共混的方法,将聚氯乙烯(PVC)与PES-g-PEGMA共混,通过溶剂-非溶剂扩散诱导相分离法(NIPS)制备PVC/PES-g-PEGMA共混膜。在此基础上对PVC/PES-g-PEGMA共混膜的断面和表面微观结构、水通量、截留率、机械性能及耐污染等性能进行测试,并采用接触角,含水率(EWC),X射线光电子能谱仪(XPS)来表征PES-g-PEGMA的质量百分含量对PVC/PES-g-PEGMA共混膜亲水性的影响。结果表明,PVC/PES-g-PEGMA共混膜水通量,亲水性较纯PVC有很大程度的提高。耐污染性实验表明,随着PES-g-PEGMA的增加,耐污染性逐渐增强。实验结果同时也表明,该共混体系最佳共混比为7∶3。     

济南市空气污染现状及控制对策

利用2013年1—12月济南市大气监测数据,分析该市空气质量现状及时空分布特征,结果表明:2013年济南市空气主要污染物质量浓度均超过《环境空气质量标准》(GB 3095—2012)二级标准限值,空气污染严重时段为冬季采暖期,颗粒物污染严重区域为该市西部和西北部地区,SO2、NO2污染严重区为中心城区,并从点源、面源和移动源3个方面提出相应的污染防治对策。在SO2、NOx和工业烟粉尘分别减排22.5%、18.2%和31.4%的条件下,运用Models-3/CMAQ模型模拟计算得出:2015年1月和7月,济南市空气中SO2、NO2、PM10和PM2.5的质量浓度与2010年同期相比将分别降低23.9%和29.7%、11.4%和15.9%、21.9%和32.6%、13.5%和26.9%,空气质量得到明显改善。     

固相萃取-气质联用法测定固体废物浸出液中的二硝基苯

建立了一种利用固相萃取法对固体废物浸出液(TCLP)中二硝基苯进行萃取,DB-5石英毛细管柱(30 m×0.25 mm×0.25μm)进行分离,质谱检测器检测二硝基苯的方法。方法在0.002 0~0.020 0 mg/L之间线性关系良好,二硝基苯三种同分异构体的检出限均为0.5μg/L,模拟样品加标回收率为93%~96%,RSD≤2%;实际固体废物样品测定的加标回收率为95%~98%。     

MoS_2/Bi_2S_3异质结光催化剂的制备及其光催化性能

以五水硝酸铋为铋源、钼酸钠为钼源、硫脲为硫源,采用简单的一步水热法合成了MoS_2/Bi_2S_3异质结光催化剂,采用XRD,SEM,TEM,BET,UV-Vis DRS技术对其进行了表征。表征结果显示,MoS_2纳米片在Bi_2S_3微棒表面生长,增加了比表面积和活性位点,并形成异质结构,促进了光生载流子的迁移,抑制了电子-空穴对的再复合。实验结果表明:钼酸钠与五水硝酸铋的质量比为1∶2时制备的复合光催化剂性能最好,反应180min时对亚甲基蓝的去除率可达96.4%,明显高于MoS_2和Bi_2S_3,且具有较高的稳定性;该催化剂对罗丹明B、甲基橙和4-硝基苯酚的去除率分别为97.1%、93.1%和90.5%,表明其对污染物具有普适性。     

一株耐盐柴油降解菌的分离鉴定及其降解性能

从某油田附近受石油污染土壤中分离出一株以柴油为惟一碳源的耐盐菌株LS1。通过对菌株的生理生化特性、菌体的形态观察及16S r DNA基因序列分析鉴定菌株LS1为假单胞菌属(pseudomonas)。该菌株可耐受的最高盐度(Na Cl)和柴油浓度分别为6%~8%和12 000 mg/L。菌株生长的适宜p H和温度条件分别为6.0~8.0和28~36℃。在盐度为6%、p H为7.0、温度为32℃、菌种投加量为10%的条件下,初始浓度为3 000 mg/L的柴油经6 d降解后,去除率可达78.3%,加入适量外加碳源葡萄糖和蔗糖,可使降解率分别提高至92%和90%左右。菌株LS1的耐盐机理可能是通过在细胞内积累甜菜碱以调节菌株细胞内外渗透压平衡。投加甜菜碱可提高耐盐菌LS1在高盐环境下对柴油的降解效率。     

Hybrid H2/Al dust explosions in Siwek sphere

Explosion indices and explosion behaviour of Al dust/H₂/air mixtures were studied using standard 20 l sphere. The study was motivated by an explosion hazard occurring at some accidental scenarios considered now in ITER design (International Thermonuclear Experimental Reactor). During Loss-of-Vacuum or Loss-of-Coolant Accidents (LOCA/LOVA) it is possible to form inside the ITER vacuum vessel an explosible atmosphere containing fine Be or W dusts and hydrogen. To approach the Be/H₂ explosion problem, Be dust is substituted in this study by aluminium, because of high toxicity of Be dusts. The tested dust concentrations were 100, 200, 400, 800, and 1200 g/m3; hydrogen concentrations varied from 8 to 20 vol. % with 2% step. The mixtures were ignited by a weak electric spark. Pressure evolutions were recorded during the mixture explosions. In addition, the gaseous compositions of the combustion products were measured by a quadruple mass-spectrometer. The dust was involved in the explosion process at all hydrogen and dust concentrations even at the combination ‘8%/100 g/m3’. In all the other tests the explosion overpressures and the pressure rise rates were noticeably higher than those relevant to pure H₂/air mixtures and pure Al dust/air mixtures. At lower hybrid fuel concentrations the mixture exploded in two steps: first hydrogen explosion followed by a clearly separated Al dust explosion. With rising concentrations, the two-phase explosion regime transits to a single-phase regime where the two fuel components exploded together as a single fuel. In this regime both the hybrid explosion pressures and pressure rise rates are higher than either H₂ or Al ones. The two fuels compete for the oxygen; the higher the dust concentration, the more part of O2 it consumes (and the more H₂ remains in the combustion products). The test results are used to support DUST3D CFD code developed at KIT to model LOCA or LOVA scenarios in ITER.     

生活垃圾与危险废物焚烧二噁英类排放特征研究

对某省52家焚烧企业(21家生活垃圾和31家危险废物)排放烟气数据进行了分析,结果表明,两类焚烧企业二噁英类17种单体分布有所不同,生活垃圾焚烧烟气中浓度较高的是O8CDD和O8CDF;危险废物焚烧烟气中较大的是2,3,4,7,8-P5CDF、2,3,7,8-T4CDD和1,2,3,7,8-P5CDD;两类焚烧企业二噁英类单体对I-TEQ贡献最高的都是2,3,4,7,8-P5CDF,贡献率分别为0. 7%～45%和10%～67%;两者的17种二噁英类与I-TEQ的相关性分析表明,1,2,3,7,8-P5CDF在2类焚烧炉中与I-TEQ均存在较高的相关性,其相关系数分别0. 932和0. 927,可以作为潜在的测定指示物。