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561.
聚硅酸对不同形态铝沉积行为的影响   总被引:2,自引:2,他引:0  
针对给水管网中残余铝沉积和再溶解现象可能引起的水质问题,研究了聚硅酸对不同水解聚合形态铝沉积、再溶解的影响,并以石英微晶天平为表征手段,初步探讨了聚硅酸对不同形态铝沉积、再溶解过程影响的机理.结果表明,聚硅酸能显著改变不同水解聚合形态铝的沉积、再溶解行为.聚硅酸可与3种水解聚合形态的铝迅速结合而生成可沉积产物,但产物性质不同.以单体形态为主的Al_0与聚硅酸的反应产物性质较稳定,部分以溶解态存在,部分以非溶解态(可沉积态)存在;尽管铝的两种聚合形态Al_(13)和Al_(30)与聚硅酸反应也生成了部分可沉积产物,但随着时间的推移,这些产物又逐渐向溶解态转化.铝硅比对Al_0体系中铝的沉积溶解行为影响较小,而对Al_(13)和Al_(30)影响较大,且在0.2∶20(以Al和SiO_2计的质量比)时,沉积态铝的溶解速率最快.  相似文献   
562.
采用超滤膜法将2-丁烯醛生产废水中的有机物分为相对分子质量不同的7个级分,并应用溶解性有机碳(dissolved organic carbon,DOC)、紫外吸收光谱(ultraviolet spectrum,UV)、傅里叶变换红外光谱(fourier transform infrared spectrometer,FT-IR)和气相色谱/质谱联用仪(gas chromatography with mass spectrometry,GC-MS)技术对不同相对分子质量区间的有机物所占比例及物质结构进行了研究.结果表明,废水中相对分子质量1×103的有机物所占比例最高,达到88.57%;采用GCMS对废水中相对分子质量1×103的级分进行分析,定性出27种化合物,包含醛、酮、酯、醇、酚、酸、烷烃类及其他苯系物等,其峰面积占有机物峰面积总和的比例分别为6.9%、5.3%、35.4%、13.2%、4.6%、0.4%、1.7%、16.8%,总和为84%.UV和FT-IR分析结果均显示不同相对分子质量区间的光谱吸收特征没有明显差别,级分中存在含有不饱和双键、羟基、羰基化合物及芳香族化合物,与GC-MS检测结果相吻合.研究结果为废水处理工艺的开发与优化提供了重要的指导作用.  相似文献   
563.
An organo-montmorillonite-supported nanoscale zero-valent iron material(M-NZVI) was synthesized to degrade decabromodiphenyl ether(BDE-209). The results showed that nanoscale zero-valent iron had good dispersion on organo-montmorillonite and was present as a core-shell structure with a particle size range of nanoscale iron between 30–90 nm, characterized by XRD, SEM, TEM, XRF, ICP-AES, and XPS. The results of the degradation of BDE-209 by M-NZVI showed that the efficiency of M-NZVI in removing BDE-209 was much higher than that of NZVI. The efficiency of M-NZVI in removing BDE-209 decreased as the pH and the initial dissolved oxygen content of the reaction solution increased, but increased as the proportion of water in the reaction solution increased.  相似文献   
564.
Catalytic oxidation is widely used in pollution control technology to remove volatile organic compounds. In this study, Pd/ZSM-5 catalysts with different Pd contents and acidic sites were prepared via the impregnation method. All the catalysts were characterized by means of N2 adsorption- desorption, X-ray fluorescence (XRF), HE temperature programmed reduction (H2-TPR), and NH3 temperature programmed desorption (NH3-TPD). Their catalytic performance was investigated in the oxidation of butyl acetate experiments. The by-products of the reaction were collected in thermal desorption tubes and identified by gas chromatography/mass spectrometry. It was found that the increase of Pd content slightly changed the catalytic activity of butyl acetate oxidation according to the yield of CO2 achieved at 90%, but decreased the cracking by-products, whereas the enhancement of strong acidity over Pd-based catalysts enriched the by-product species. The butyl acetate oxidation process involves a series of reaction steps including protolysis, dehydrogenation, dehydration, cracking, and isomerization. Generally, butyl acetate was cracked to acetic acid and 2- methylpropene and the latter was an intermediate of the other by-products, and the oxidation routes of typical by-products were proposed. Trace amounts of 3-methylpentane, hexane, 2-methylpentane, pentane, and 2-methylbutane originated from iso4merization and protolysis reactions.  相似文献   
565.
Plastics such as polyvinyl chlorides (PVC) are widely used in many indoor constructed environments; however, their unbound chemicals, such as di-(2-ethylhexyl) phthalates (DEHP), can leach into the surrounding environment. This study focused on DEHP's effect on the central nervous system by determining the precise DEHP content in mice brain tissue after exposure to the chemical, to evaluate the specific exposure range. Primary neuronal-astrocyte co-culture systems were used as in vitro models for chemical hazard identification of DEHP. Oxidative stress was hypothesized as a probable mechanism involved, and therefore the total reactive oxygen species (ROS) concentration was determined as a biomarker of oxidative stress. In addition, NeuriteTracer, a neurite tracing plugin with ImageJ, was used to develop an assay for neurotoxicity to provide quantitative measurements of neurological parameters, such as neuronal number, neuron count and neurite length, all of which could indicate neurotoxic effects. The results showed that with 1 nmol/L DEHP exposure, there was a significant increase in ROS concentrations, indicating that the neuronal-astrocyte cultures were injured due to exposure to DEHP. In response, astrocyte proliferation (gliosis) was initiated, serving as a mechanism to maintain a homeostatic environment for neurons and protect neurons from toxic chemicals. There is a need to assess the cumulative effects of DEHP in animals to evaluate the possible uotake and effects on the human neuronal system from exoosure to DEHP in the indoor environment.  相似文献   
566.
Bioaerosols from wastewater treatment processes are a significant subgroup of atmospheric aerosols. In the present study,airborne microorganisms generated from a wastewater treatment station(WWTS) that uses an oxidation ditch process were diminished by ventilation.Conventional sampling and detection methods combined with cloning/sequencing techniques were applied to determine the groups,concentrations,size distributions,and species diversity of airborne microorganisms before and after ventilation. There were 3021 ± 537 CFU/m3 of airborne bacteria and 926 ± 132 CFU/m3 of airborne fungi present in the WWTS bioaerosol.Results showed that the ventilation reduced airborne microorganisms significantly compared to the air in the WWTS. Over 60% of airborne bacteria and airborne fungi could be reduced after4 hr of air exchange. The highest removal(92.1% for airborne bacteria and 89.1% for fungi) was achieved for 0.65–1.1 μm sized particles. The bioaerosol particles over 4.7 μm were also reduced effectively. Large particles tended to be lost by gravitational settling and small particles were generally carried away,which led to the relatively easy reduction of bioaerosol particles0.65–1.1 μm and over 4.7 μm in size. An obvious variation occurred in the structure of the bacterial communities when ventilation was applied to control the airborne microorganisms in enclosed spaces.  相似文献   
567.
This study investigated the filtration and continuous regeneration of a particulate filter system on an engine test bench, consisting of a diesel oxidation catalyst(DOC) and a catalyzed diesel particulate filter(CDPF). Both the DOC and the CDPF led to a high conversion of NO to NO2 for continuous regeneration. The filtration efficiency on solid particle number(SPN) was close to100%. The post-CDPF particles were mainly in accumulation mode. The downstream SPN was sensitively influenced by the variation of the soot loading. This phenomenon provides a method for determining the balance point temperature by measuring the trend of SPN concentration.  相似文献   
568.
通过序批实验的方法,直接接种厌氧氨氧污泥,研究了Zn2+对厌氧氨氧化(Anammox)脱氮效能的影响。研究结果表明,当进水Zn2+质量浓度小于2 mg/L时,对厌氧氨氧化生物活性有促进作用,可增强微生物的脱氮效能;当进水Zn2+质量浓度在2 mg/L和4 mg/L之间时,脱氮效能无明显变化,说明对厌氧氨氧化微生物活性无明显影响;当进水Zn2+质量浓度大于4 mg/L,对厌氧氨氧化反应有抑制作用,Zn2+浓度越高,抑制作用越明显。 Zn2+对厌氧氨氧化的半抑制质量浓度(CI,50)为32.3 mg/L,NO2--N与NH4+-N转化比的平均值为1.28。  相似文献   
569.
江苏如东互花米草盐沼湿地重金属分布及其污染评价   总被引:3,自引:1,他引:2  
为了解互花米草(Spartina alterniflora)对盐沼湿地环境的影响,于2010年7月在江苏如东潮间带,依据互花米草的有无及其长势设置站点,对表层沉积物的8种重金属含量、粒度组成、总有机碳进行分析,采用地累积指数法(Igeo)和Hkanson潜在生态风险指数法进行污染评价.结果表明,如东滩涂表层沉积物中Pb、Cd、As、Hg、Cr、Cu、Ni、Zn的平均含量低于海洋沉积物标准I类,其中Cd、Hg、Ni、Zn的含量高于中国大陆沉积物-浅海粉砂背景值.整体上,8种元素在米草覆盖区平均含量均高于邻近光滩.地累积指数显示该盐沼带重金属为无污染状态,而Hkanson潜在生态风险评价显示为低污染和中度污染的临界状态,风险指数为低;两方法均显示该区域污染以Cd和Hg最重.由海向陆随米草长势渐好(垂直岸线断面),As、Cu及Hg元素的含量、地累积指数、潜在生态风险系数呈渐增趋势;拓殖1年左右的米草斑块区内(平行岸线断面),8种元素在植被覆盖区的含量、污染程度及潜在生态风险均高于邻近无植被覆盖区.此外,斑块分布区中,Cd、Cu含量显著低于垂直断面的茂盛分布区.互花米草是大部分重金属污染物在沉积物中富集的重要驱动力之一,且互花米草群落可阻滞污染物直接扩散入海,因而降低生态危害.互花米草对重金属分布的影响与米草的拓植年限、金属元素存在形态和来源有关.  相似文献   
570.
活性炭催化过氧化氢去除荧光增白剂   总被引:1,自引:1,他引:0  
刘海龙  张忠民  赵霞  焦茹媛 《环境科学》2014,35(6):2201-2208
研究了活性炭(activated carbon,AC)吸附、改性活性炭(activated carbon modified,ACM)吸附、过氧化氢(H2O2)氧化、AC催化H2O2等方法对水体中荧光增白剂VBL的处理效果,并通过自由基俘获剂叔丁醇、催化过程气体分析等探讨了AC催化H2O2分解VBL的机制.结果表明,经硝酸铁[Fe(NO3)3]改性过的ACM对VBL的吸附去除率高于未改性的AC.活性炭催化H2O2对VBL的去除效果明显,但未改性AC催化去除率高于ACM.60 min时,AC催化氧化去除率即可达到95%以上,而ACM仅为58%.叔丁醇的加入降低了AC和ACM催化氧化对VBL的去除率,表明AC催化H2O2氧化能促进H2O2形成羟基自由基(·OH)和原子氧参与反应.AC催化H2O2分解及释放气体分析表明,AC能催化H2O2形成氧气并放热,且ACM明显快于AC.结合催化H2O2去除VBL效率的结果分析,ACM催化反应时活性中间物(自由基和原子氧等)产生速率快于AC,活性中间物自身消耗形成氧气,而不是用于分解VBL.催化反应中活性中间产物的形成速率与反应物供给速率的不匹配可能是导致ACM催化效果弱于AC的重要原因.  相似文献   
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