液体吸收-活性炭吸附净化苯乙烯废气

介绍了液体吸收-活性炭吸附净化苯乙烯废气的原理.当吸收液中石油类物质占总体积的40％时吸收率最佳,小试液体吸收段对苯乙烯废气的吸收率在74％-97.6％之间,在工业净化装置中使用该吸收液,对苯乙烯废气的吸收率在60％-97.4％之间.活性炭对苯乙烯的吸附率为自重的30％.工业净化装置中,两种方法并用苯乙烯废气的净化效率在94.8％以上.该方法关键是寻找高效的吸收液和设计实用的净化装置.     

天津地区大气污染状况和气溶胶硫酸盐的研究

我们于1980—1981年对天津市大气污染物浓度做了同步监测,对天津市大气污染状况,二氧化硫转化为硫酸盐的过程及其对大气能见度的影响做了研究。以超C_i几率和的方法处理数据,研究结果表明,大气污染以早晨最严重,傍晚次之,中午较轻:冬季比夏季污染严重。各种污染物中以硫酸盐对大气能见度的影响最大,总颗粒物次之。当大气相对湿度大于70%时,对大气能见度的影响比较突出。颗粒物中的苯溶物对大气能见度有一定的影响。城市中相对湿度高时硫酸盐浓度大,可能是产生冬季烟雾事件的原因。下风方向的硫酸根浓度与二氧化硫浓度的比值和硫酸根含硫浓度与大气总硫浓度的比值均比上风方向相应的数值高,说明城市燃煤烟气是硫酸盐的来源。城市中硫酸根浓度与二氧化硫浓度的相关系数为0.77,硫酸根与颗粒物浓度的相关系数为0.95。在形成硫酸根的过程中二氧化硫浓度和颗粒物可能有贡献。以一维有源简化模式估算二氧化硫转化为硫酸根的速率常数,约为2.3±1.1%/hr,冬季约1.5%/hr。二氧化硫的迁移距离约为17—340km。     

pH过程控制对铁炭微电解-Fenton影响中试研究

采用铁炭微电解-Fenton联合工艺处理制药废水生化出水,探讨了初始pH对微电解过程COD降解速率、出水中Fe2+和Fe3+变化规律以及后续Fenton氧化效果的影响,为优化联合工艺提出了微电解反应pH过程控制的理论。采用pH过程控制时,微电解对COD降解速率大大提高,降解过程基本符合零级反应动力学,同时可大大提高Fe2+和Fe3+浓度及总铁析出量。试验结果表明:当初始pH=2.5,以3.0L/h连续性投加稀硫酸100 min,曝气微电解反应2 h,出水再投加1.0mL/L的H2O2进行Fenton氧化2 h,出水COD总去除率可达85.6%;采用pH过程控制可将微电解出水ρ(Fe2+)浓度从48.6 mg/L提高至149 mg/L,COD降解速率从10.9 mg/(L·h)提高至23.8 mg/(L·h)。     

3株反硝化聚磷菌的分离与鉴定

通过烛缸法培养富集、分离,结合除磷试验、硝酸盐还原产气试验及异染颗粒和PHB颗粒染色辅助检验相结合的方法筛选,得到3株具有较高脱氮除磷效率的反硝化聚磷菌DNPA8, DNPA9和DNPA10。在富氮富磷培养基中培养48 h,各菌株的脱氮率均大于75%,除磷率均大于78%。采用多相分类的方法确定了3株反硝化聚磷菌的分类地位,DNPA8为嗜麦芽寡养单胞菌,DNPA9为水生丛毛单胞菌属首次发现的反硝化聚磷菌;DNPA10为约翰逊氏不动杆菌。该研究结果为富营养化水体的治理提供了有效的菌种资源。     

Emission of intermediate volatility organic compounds from a ship main engine burning heavy fuel oil

Intermediate volatility organic compounds (IVOCs) are crucial precursors of secondary organic aerosol (SOA). In this study, gaseous IVOCs emitted from a ship main engine burning heavy fuel oil (HFO) were investigated on a test bench, which could simulate the real-world operations and emissions of ocean-going ships. The chemical compositions, emission factors (EFs) and volatility distributions of IVOC emissions were investigated. The results showed that the main engine burning HFO emitted a large amount of IVOCs, with average IVOC EFs of 20.2–201?mg/kg-fuel. The IVOCs were mainly comprised of unspeciated compounds. The chemical compositions of exhaust IVOCs were different from that of HFO fuel, especially for polycyclic aromatic compounds and alkylcyclohexanes. The volatility distributions of IVOCs were also different between HFO exhausts and HFO fuel. The distinctions in IVOC emission characteristics between HFO exhausts and HFO fuel should be considered when assessing the IVOC emission and related SOA formation potentials from ocean-going ships burning HFO, especially when using fuel-surrogate models.     

持续放牧和围封对科尔沁退化沙地草地碳截存的影响

研究了科尔沁退化沙地草地持续放牧和围封恢复下土壤-植物系统的碳(C)贮存,以揭示草地管理对C动态的影响.结果表明,0～15cm土壤OC和植物系统贮存的C(包括初级生产固定的C,立枯和地表凋落物C和根系C)贮量大小为:围封10年草地(584g·m^-2和309 g·m^-2)＞围封5年草地(524g·m^-2和146g·m^-2)＞持续放牧草地(493g·m^-2和95 g·m^-2).在围封10年,围封5年和持续放牧草地中,0～15cm土壤贮存C分别占各自土壤-植物系统C的65.3%,78.2%和83.9%.在风蚀严重的科尔沁沙地,持续放牧对植被,土壤及其周围环境有极严重的恶化作用.采取围封恢复措施后,植被恢复和凋落物积累使土壤免遭风蚀,也显著增加了土壤有机质的输入,因而显著作用于大气C的截存.但排除家畜放牧的长期围封使植物C向土壤C的再循环受到限制,截存的大部分C以凋落物的形式积存在土壤表面,需进一步深入研究围封的时间尺度.研究结果表明,退化沙地草地在采取有效的保护措施后,可以由C源变为C汇.     

大麻茎腐病菌的分离及其对土壤环境影响的研究

从病变部位分离出两株病原真菌DN1和DN2,通过茵丝及孢子形态的观察,初步确定其分别为半知菌亚门链格孢属（Altemaria altemata）及轮枝孢属（M．Verticillium）。在pH值4～14之间,两株菌都能正常生长,对环境的适应能力较强。通过盆栽试验确定大麻对土壤pH的影响,结果表明大麻能修复弱碱性土壤。     

Ultrasonic preparation of nano-nickel/activated carbon composite using spent electroless nickel plating bath and application in degradation of 2,6-dichlorophenol

Ni was effectively recovered from spent electroless nickel （EN） plating baths by forming a nano-nickel coated activated carbon composite. With the aid of ultrasonication, melamine- formaldehyde-tetraoxalyl-ethylenediamine chelating resins were grafted on activated carbon （MFT/AG）. PdC12 sol was adsorbed on MFT/AC, which was then immersed in spent electroless nickel plating bath; then nano-nickel could be reduced by ascorbic acid to form a nano-nickel coating on the activated carbon composite （Ni/AC） in situ. The materials present were carefully examined by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, X-ray photoelectron spectroscopy and electro- chemistry techniques. The resins were well distributed on the inside and outside surfaces of activated carbon with a size of 120 ± 30 nm in MFT/AC, and a great deal of nano-nickel particles were evenly deposited with a size of 3.8 ± 1.1 nm in Ni/MFT. Moreover, Ni/AC was successfully used as a catalyst for ultrasonic degradation of 2.6-dichloronhenol.     

Mercury flows in large-scale gold production and implications for Hg pollution control

Large-scale gold production(LSGP) is one of the five convention-related atmospheric mercury(Hg) emission sources in the Minamata Convention on Mercury. However, field experiments on Hg flows of the whole process of LSGP are limited. To identify the atmospheric Hg emission points and understand Hg emission characteristics of LSGP, Hg flows in two gold smelters were studied. Overall atmospheric Hg emissions accounted for 10%–17% of total Hg outputs and the Hg emission factors for all processes were 7.6–9.6 kg/ton. There were three dominant atmospheric Hg emission points in the studied gold smelters, including the exhaust gas of the roasting process, exhaust gas from the environmental fog collection stack and exhaust gas from the converter of the refining process. Atmospheric Hg emissions from the roasting process only accounted for 16%–29% of total emissions and the rest were emitted from the refining process. The overall Hg speciation profile(gaseous elemental Hg/gaseous oxidized Hg/particulate-bound Hg) for LSGP was 34.1/57.1/8.8. The dominant Hg output byproducts included waste acid, sulfuric acid and cyanide leaching residue. Total Hg outputs from these three byproducts were 80% in smelter A and 84% in smelter B. Our study indicated that previous atmospheric Hg emissions from large-scale gold production might have been overestimated.Hg emission control in LSGP is not especially urgent in China compared to other significant emission sources(e.g., cement plants). Instead, LSGP is a potential Hg release source due to the high Hg output proportions to acid and sludge.     

铅锌冶炼弃渣有害特征及其浸出行为研究

铅锌弃渣是有色金属工业排出的大宗固体废物之一。其中有铅冶炼系统排铅烟花炉渣,锌系统排锌回转窑渣。铅锌弃渣一般含有多种超过排放标准而目前又尚无成熟工艺提取的有价值和稀贵金属元素。这些废渣的堆存直接影响自然景观,并有可能对环境如土壤、水体和作物等造成危害。因此,考察铅锌渣的有害特征,研究其水浸出行为与规律,对解决铅锌弃渣对环境污染,寻求同行业固体废物的治理途径具有重要的现实意义。