生物炭和碳纳米管固定化漆酶去除水体雌二醇

漆酶是一类具有高效的催化氧化能力的含铜多酚的氧化酶,而固定化漆酶技术在有机废水处理领域受到了越来越多的关注。通过比较吸附法和包埋法利用木炭(WB)、竹炭(BB)和碳纳米管(CNT)固定游离漆酶去除水体雌二醇(E2)。在25 °C 、pH=5条件下,固定化漆酶经120 h 贮存仍保留80%的活性。经过5次循环研究,固载的漆酶仍保留了27%~58%的剩余活性。结合扫描电子显微镜和傅里叶变换红外光谱,证实了漆酶成功地负载在碳基材料上。仅在 8 h内,50 mg·L⁻¹ E2通过吸附法制备的WB、BB、CNT固定化漆酶去除了42.92%、47.66%、43.92%,而包埋法制备的WB、BB、CNT固定化漆酶分别去除84.08%、87.20%、87.86%。结果表明,包埋法固定化漆酶对E2的去除效率更优,这是由于包埋固载在生物炭和CNT的漆酶更为稳定。此外,K⁺和Mn²⁺离子可能通过干扰漆酶的电子传递过程影响漆酶的活性,从而抑制E2的去除。本研究旨在为固定化漆酶在有机废水处理的实际应用提供指导。     

填料塔应用于烟道气治理时设计中应注意的问题探讨

论述了填料塔烟道气治理装置的填料层及塔内件的设计,并和传统的塔型尺寸及各种参数进行了比较。     

Fractionation of fulvic acids: characteristics and complexation with copper

Two fulvic acid samples isolated from Suwannee river (International Humic Substance Society) and Feeitsuey reservoir were subjected to gel filtration chromatography (GFC) for molecular size fractionation. The GFC-eluted samples were separated into three groups corresponding to the molecular weight ranges: < 220, 220-1000, and 1000-4000. Fluorescence quenching techniques were employed for determining the conditional stability coefficient and kinetic parameters of copper complexation with the three fractions of fulvic acids. Experimental conditions were pH 6, 5 x 10(-5)m total copper and 5 mg C litre(-1) of fulvic acids. The conditional stability coefficients of the fulvic acid fractions were in the order of 0.9-3.3 x 10(5)m(-1), and the forward and reverse rate constants were in the order of 6.9-12.4 x 10(3)m(-1) s(-1) and 3.5-8.0 x 10(-2) s(-1). Information could be useful in modelling copper transport in the hydrosphere.     

Atmospheric polycyclic aromatic hydrocarbons (PAHs) in Asia: a review from 1999 to 2004

Polycyclic aromatic hydrocarbons (PAHs) are present in both gaseous and particulate phases. These compounds are considered to be atmospheric contaminants and are human carcinogens. Many studies have monitored atmospheric particulate and gaseous phases of PAH in Asia over the past 5 years. This work compares and discusses different sample collection, pretreatment and analytical methods. The main PAH sources are traffic exhausts (AcPy, FL, Flu, PA, Pyr, CHR, BeP) and industrial emissions (BaP, BaA, PER, BeP, COR, CYC). PAH concentrations are highest in areas of traffic, followed by the urban sites, and lowest in rural sites. Meteorological conditions, such as temperature, wind speed and humidity, strongly affect PAH concentrations at all sampling sites. This work elucidates the characteristics, sources and distribution, and the healthy impacts of atmospheric PAH species in Asia.     

Organochlorine pesticides in soil profiles from Tianjin, China

Soil cores were collected from soils at five sites in Tianjin area for the determination of hexachlorocyclohexane isomers (HCHs, including alpha-HCH, beta-HCH, gamma-HCH and delta-HCH), dichlorodiphenyltrichloroethane and metabolites (DDXs, including p,p'-DDT, p,p'-DDE and p,p'-DDD) and total organic carbon (TOC). The levels and vertical distributions of HCHs and DDXs are studied. Results show that the application of pesticides in the past years was the major contributor of HCHs and DDXs accumulation in the sampling areas. Significant positive correlations were seen between the residual and application amounts of HCHs and DDXs. Wastewater irrigation did not bring a significant contribution of HCHs or DDXs into the soils. HCHs and DDXs concentrations peak at the surface and decline in soil profile with depth, while fluctuations were observed in the plow layers of some cultivated soils caused by frequent cultivation activities and batch irrigation. Positive correlations were observed between the contents of TOC and HCHs and DDTs. Although the amounts of HCHs application in all sampling sites are larger than DDXs, at surface and near surface layers of most sampling sites, the concentrations of summation operatorHCHs are lower than summation operatorDDXs. The composition of DDXs in the applied pesticides and sampled soils indicates that there is no recent DDT input at the sample areas.     

Adsorption characteristics of benzene on biosolid adsorbent and commercial activated carbons

This study selected biosolids from a petrochemical waste-water treatment plant as the raw material. The sludge was immersed in 0.5-5 M of zinc chloride (ZnCl2) solutions and pyrolyzed at different temperatures and times. Results indicated that the 1-M ZnCl2-immersed biosolids pyrolyzed at 500 degrees C for 30 min could be reused and were optimal biosolid adsorbents for benzene adsorption. Pore volume distribution analysis indicated that the mesopore contributed more than the macropore and micropore in the biosolid adsorbent. The benzene adsorption capacity of the biosolid adsorbent was 65 and 55% of the G206 (granular-activated carbon) and BPL (coal-based activated carbon; Calgon, Carbon Corp.) activated carbons, respectively. Data from the adsorption and desorption cycles indicated that the benzene adsorption capacity of the biosolid adsorbent was insignificantly reduced compared with the first-run capacity of the adsorbent; therefore, the biosolid adsorbent could be reused as a commercial adsorbent, although its production cost is high.     

二步法腈纶生产废水的处理试验

本试验采用混凝 -A/O系统组合工艺处理二步法腈纶废水 ,该系统处理效果良好 ,出水水质符合排放标准 ,可直接排入水体。A/O系统试验装置总容积 80L ,水力停留时间 5 8— 70h ,缺氧池与好氧池的容积比为 1∶3 ,回流比 ( 2—3 )∶1,COD和BOD总去除率分别约为 84%和 98%。     

Single particle mass spectrometry of oxalic acid in ambient aerosols in Shanghai: Mixing state and formation mechanism

Oxalic acid in individual aerosol particles was measured using single particle aerosol time-of-flight mass spectrometry (ATOFMS) in the summer of 2007 in Shanghai, China. Oxalate was found in 3.4% of total particles with diameters in the range of 0.2 – 2.0 μm. Size, chemical composition and hourly temporal counts of single particles that contained oxalic acid were measured. The predominant types of oxalate-containing particles were characterized to distinguish the primary and secondary sources of oxalic acid. Biomass burning was revealed as a major primary source of oxalic acid which contributed more than 20% of the oxalate-containing particles. Evidences for two different formation pathways of oxalic acid were observed in our experiment. The number fraction of oxalate-containing particles correlated with that of sulfate particles and the changes of air parcel backward trajectories, suggesting that in-cloud processing played important roles in oxalic acid formation. The diurnal patterns of dust and sea salt particle counts fitted well with the ambient relative humidity variation, suggesting that heterogeneous reactions occurring in hydrated/deliquesced aerosols also contributed to the production of oxalic acid.     

四种净水工艺对水源水微量有机物去除的研究

以UV254和CODMn代表饮用水源水中有机物替代指标.对常规处理、生物陶粒预处理、生物滤池、生物活性炭(BAC)、颗粒活性炭(GAC)、纳滤和光催化氧化进行组合,形成不同的处理流程,研究各流程对UV254和CODMn的去除效果.结果表明,各工艺流程都有一定的处理效率,其中以生物滤池和纳滤为主的组合流程处理效果最佳.此流程对UV254的去除率接近100%,CODMn的去除率达到78.6%,大大提高了饮用水的安全性.     

生物接触氧化结合气浮法处理卷烟综合废水

某卷烟厂采用生物接触氧化结合气浮法处理卷烟综合废水,经过3年的运行实践表明,工艺运行稳定可靠,在进水COD为300～1 500 mg/L、SS为100～600 mg/L、BOD5为100～900 mg/L、NH3-N为10～20 mg/L、水温为20～30 ℃时,出水COD《70 mg/L、BOD5《20 mg/L、SS《30 mg/L、NH3-N《3 mg/L,完全实现达标排放.