高锰酸盐复合药剂预氧化缓解超滤膜藻类污染的中试研究

通过中试试验考察了高锰酸盐复合药剂(PPC)预氧化强化混凝/沉淀/超滤的组合工艺的除藻效能以及PPC预氧化对藻类引起的膜污染的缓解作用,并对其机理进行了探讨.试验结果表明,投加0.6mg·L-1PPC能使预处理阶段对藻类的平均去除率提高约28%.组合工艺处理高藻水时,PPC预氧化通过强化预处理,降低膜表面的污染负荷,对藻源污染物引起可逆和不可逆污染均具有一定的缓解作用.化学清洗试验结果表明,碱洗对超滤膜TMP恢复效果远远强于酸洗,因而有机物是超滤膜处理高藻水时的主要污染物质.     

气相色谱法测定地下水的乙醇和单环芳香烃

探讨了同时测定地下水中乙醇和单环芳香烃的顶空气相色谱方法。水中的乙醇和微量芳香烃经过顶空提取后,应用HP-5毛细管色谱柱,利用分流与不分流进样口进样,同时采用程序升温方式进行GC分析,以保留时间定性,外标法定量。研究结果表明,乙醇、苯、甲苯、乙苯、对二甲苯和间二甲苯、邻二甲苯的线性范围分别为0.38~189.36mg/L、6.0~1500.0μg/L、6.0~1500.0μg/L、6.0~1500.0μg/L、12.0~3000.0μg/L和6.0~1500.0μg/L,最低检出浓度为137.14μg/L、0.62μg/L、0.55μg/L、0.51μg/L、0.51μg/L和0.59μg/L,水样加标回收率为91.91%L~106.35%L,RSD为2.79%L~3.76%L。表明该方法一次性完成地下水中乙醇和单环芳香烃的分离和测定,分析时间仅为15min,操作简便、灵敏。     

含氚硅胶密封包装实验研究

文章针对含氚硅胶,设计了双层桶密封包装容器,即以镀膜铝桶为初始包装,内衬高密度聚乙烯(HDPE)不锈钢桶为外包装容器。含氚硅胶在镀膜铝桶内用环氧树脂浇注固定,密封;铝桶放入衬HDPE不锈钢外桶,间隙蛭石填充,垫圈密封。含氚硅胶包装桶氚释气率测量结果表明,20天内日均释氚率为4.62×10-5%;浸出实验结果表明,108天内氚日均浸出率远小于10-3%,满足氚废物包装的相关要求。     

悬浮物对半滑舌鳎稚鱼的急性毒性效应

研究了不同浓度悬浮物对半滑舌鳎(Cynoglossus semilaevisG櫣nther)浮游阶段和伏底阶段稚鱼的急性毒性效应。实验结果表明,悬浮物对浮游阶段稚鱼的48 hLC50和96 hLC50(95%可信限)分别为588.2 mg/L(518.7~666.9 mg/L)和488.7 mg/L(428.6~557.2 mg/L),安全浓度(SC)为48.87 mg/L;水温(tw)为23℃时,对伏底阶段稚鱼的48 hLC50和96 hLC50(95%可信限)分别为3 034.6 mg/L(2769.8~3324.8 mg/L)和2117.2 mg/L(1932.1~2320.1 mg/L),SC为211.72mg/L;tw为26℃时,对伏底阶段稚鱼的48 hLC50和96 hLC50(95%可信限)分别为1684.0 mg/L(1543.4~1837.3 mg/L)和1657.1 mg/L(1522.7~1803.4 mg/L),SC为165.71 mg/L。     

石化行业水环境污染事件分级初探

为规范应急管理工作,提高突发事件的应急救援反应速度和协调水平,增强综合处置重特大事件的能力,预防和控制次生灾害的发生,保障企业员工和公众的生命安全,最大限度地减少财产损失、环境破坏和社会影响,中国石化制定了《中国石化重特大事件应急预案》。     

大气环境质量现状评价模型存在的问题及改进——以沈阳大气指数模型为例

文章分析了几类大气环境质量现状评价模型各自存在的问题,针对这些问题,选择了较典型的沈阳大气指数模型,首先对原模型中参数进行修正,使其成为与当前执行的环境空气质量标准相对应的综合指数模型,其次,基于概率统计思想对模型进行改进,得到不同保证率下的大气环境质量现状评价模型,最后,运用SPSS软件进行实证分析,改进后模型得到的评价结果更能准确反映区域实际大气环境质量现状。     

Isolation and characteristics of a novel biphenyl-degrading bacterial strain, Dyella ginsengisoli LA-4

A novel biphenyl-degrading bacterial strain LA-4 was isolated from activated sludge. It was identified as Dyella ginsengisoli according to phylogenetic similarity of 16S rRNA gene sequence. This isolate could utilize biphenyl as sole source of carbon and energy, which degraded over 95 mg/L biphenyl within 36 h. The major metabolites formed from biphenyl, such as 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid (HOPDA) and benzoic acid, were identified by LC-MS. The crude cell extract of strain LA-4 exhibited the activity of 2,3-dihydroxybiphenyl 1,2-dioxygenase (2,3-DHBD) and the kinetic parameters were Km= 26.48 μmol/L and Vmax= 8.12 μmol/mg protein. A conserved region of the biphenyl dioxygenase gene bphA1 of strain LA-4 was amplified by PCR and confirmed by DNA sequencing.     

Identification and characterization of the chromium（Ⅵ） responding protein from a newly isolated Ochrobactrum anthropi CTS-325

A Gram-negative, chromium(VI) tolerant and reductive strain CTS-325, isolated from a Chinese chromate plant, was identified as Ochrobactrum anthropi based on its biochemical properties and 16S rDNA sequence analysis. It was able to tolerate up to 10 mmol/L Cr(VI) and completely reduce 1 mmol/L Cr(VI) to Cr(III) within 48 h. When the strain CTS-325 was induced with Cr(VI), a protein increased significantly in the whole cell proteins. Liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis revealed that this protein was a superoxide dismutase (SOD) homology. The measured superoxide dismutase activity was 2694 U/mg after three steps of purification. The SOD catalyzes the dismutation of the superoxide anion (O₂^·−) into hydrogen peroxide and molecular oxygen. This protein is considered to be one of the most important anti-oxidative enzymes for O. anthropi as it allows the bacterium to survive high oxygen stress environments, such as the environment produced during the reduction process of Cr(VI).     

低分子量有机酸对岩源磷释放的实验研究

低分子量有机酸是微生物和植物根系分泌物中重要的组成部分.采用浸泡实验比较了4种常见低分子量有机酸(草酸、酒石酸、柠檬酸、苹果酸)对巢湖北岸东部富磷地层中岩源磷的释放量,并对浸提后的部分残渣进行磷的赋存形态分析.结果表明,当有机酸浓度小于5mmol·L-1时,柠檬酸的释磷量最大;大于5mmol·L-1时,草酸和酒石酸的释磷量最大,此时释磷量与有机酸的浓度具有一定的线性关系,其增加趋势远大于浓度小于5mmol·L-1时的增加趋势,而其中草酸和酒石酸又远大于柠檬酸和苹果酸.在有机酸溶液终止pH≥4时,有机酸溶液终止pH与释磷量有较好的线性关系.在50mmol·L-1相同浓度时,草酸对各赋存形态磷转化作用均最大,酒石酸次之.而4种酸对有机磷释放率最大,均高达97%以上,对闭蓄态磷的释放率最小.     

Iron-doped Mn-Ce/TiO2 catalyst for low temperature selective catalytic reduction of NO with NH3

The catalysts of iron-doped Mn-Ce/TiO 2(Fe-Mn-Ce/TiO 2) prepared by sol-gel method were investigated for low temperature selective catalytic reduction(SCR) of NO with NH 3.It was found that the NO conversion over Fe-Mn-Ce/TiO 2 was obviously improved after iron doping compared with that over Mn-Ce/TiO 2.Fe-Mn-Ce/TiO 2 with the molar ratio of Fe/Ti = 0.1 exhibited the highest activity.The results showed that 96.8% NO conversion was obtained over Fe(0.1)-Mn-Ce/TiO 2 at 180°C at a space velocity of 50,000 hr 1.Fe-Mn-Ce/TiO 2 exhibited much higher resistance to H 2 O and SO 2 than that of Mn-Ce/TiO 2.The properties of the catalysts were characterized using X-ray diffraction(XRD),N 2 adsorption,temperature programmed desorption(NH 3-TPD and NOx-TPD),and Xray photoelectron spectroscopy(XPS) techniques.BET,NH3-TPD and NOx-TPD results showed that the specific surface area and NH3 and NOx adsorption capacity of the catalysts increased with iron doping.It was known from XPS analysis that iron valence state on the surface of the catalysts were in Fe3+ state.The doping of iron enhanced the dispersion and oxidation state of Mn and Ce on the surface of the catalysts.The oxygen concentrations on the surface of the catalysts were found to increase after iron doping.Fe-Mn-Ce/TiO2 represented a promising catalyst for low temperature SCR of NO with NH3 in the presence of H2 O and SO2.