泥龄对A~2O工艺去除多环麝香的影响

研究了A2O工艺不同污泥龄(Sludge retention time,SRT)条件下中佳乐麝香(Galaxolide,HHCB)与吐纳麝香(Tonalide,AHTN)的去除和迁移的变化情况。采用固相萃取与气相质谱联用的方法对各池中水相与泥相中HHCB和AHTN的浓度进行分析。结果发现:A2O工艺对HHCB的去除效果好于AHTN。高SRT条件(15,20 d)下HHCB、AHTN的总去除率明显小于低SRT条件(5,10 d)下的总去除率。     

Adsorption of 2-mercaptobenzothiazole from aqueous solution by organo-bentonite

The adsorption behavior of 2-mercaptobenzothiazole onto organo-bentonite was investigated.Natural bentonite from Gaozhou in Guangdong Province,China was collected.Organo-bentonite was prepared by intercalation of cetyltrimethyl ammonium bromide into the natural bentonite.The physicochemical properties of the prepared organo-bentonite were characterized by X-ray diffraction,N2 adsorption-desorption isotherm and Fourier transform infrared spectroscopy.The results showed that montmorillonite is the main component of the natural bentonite.The basal spacing of the natural bentonite is 1.47 nm,which increased to 1.98 nm on intercalation with cetyltrimethyl ammonium bromide.Moreover,both the surface area and pore volume increased with intercalation.Clear CH2 stretching(3000-2800 cm-1) and scissoring(1480-1450 cm-1) modes of the intercalated surfactants were observed for organobentonite.Compared with the pseudo first-order kinetic model,the pseudo second-order kinetic model is more suitable to describe the adsorption kinetics of 2-mercaptobenzothiazole onto organo-bentonite.The adsorption capacity of 2-mercaptobenzothiazole onto organo-bentonite increased with increasing initial concentration of 2-mercaptobenzothiazole,but decreased with increasing adsorbent dosage.The adsorption isotherm of 2-mercaptobenzothiazole onto organo-bentonite fits well with the Langmuir model.The maximum adsorption capacity of organo-bentonite for 2-mercaptobenzothiazole was 33.61 mg/g,indicating that organo-bentonite is a promising adsorbent for 2-mercaptobenzothiazole.     

Photocatalytic activity of TiO2 containing anatase nanoparticles and rutile nanoflower structure consisting of nanorods

A series of TiO2 with different crystal phases and morphologies was synthesized via a facile hydrothermal process using titanium nbutoxide and concentrated hydrochloric acid as raw materials. The photocatalytic activity of the samples was evaluated by degradation of Methyl Orange in aqueous solution under UV-Visible light irradiation. On the basis of detailed analysis of the characterizing results of high-resolution transmission electron microscopy, X-ray powder diffraction measurements, X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller measurement, it was concluded that the photo-activity of the catalyst is related directly to the 3D morphology and the crystal phase composition. An excellent catalyst should have both a futile 3D flower-like structure and anatase granulous particles. The 3D flower-like structure could enhance light harvesting, as well as the transfer of reactant molecules from bulk solution to the reactive sites on TiO2. In addition, the optimum anatase/rutile phase ratio was found to be 80：20, which is beneficial to the effective separation of the photogenerated electron-hole pairs.     

Effects of physical and chemical characteristics of surface sediments in the formation of shallow lake algae-induced black bloom

Surface sediments are closely related to lake black blooms. The dissolved oxygen （DO） distribution and its penetration depth in surface sediments as well as the migration and transformation of redox sensitive elements such as Fe and S at the sediment-water interface are important factors that could influence the formation of the black bloom. In this study, dredged and undredged sediment cores with different surface properties were used to simulate black blooms in the laboratory. The Micro Profiling System was employed to explore features of the DO and ∑H2S distribution at the sediment-water interface. Physical and chemical characteristics in sediments and pore waters were also analyzed. The results showed that sediment dredging effectively suppressed the black blooms. In the undredged treatment, DO penetration depth was only 50 μm. Fe^2＋ concentrations, ∑H2S concentrations, and ∑H2S production rates were remarkably higher in surface sediments and pore waters compared to control and dredged treatments. Furthermore, depletion of DO and accumulation of Fe^2＋ and ∑H2S in surface sediments and pore waters provided favorable redox environments and necessary material sources for the blooms. The study results proved that physical and chemical characteristics in surface sediments are important factors in the formation of the black bloom, and could provide scientific guidance for emergency treatment and long-term pre-control of black blooms.     

Iron and lead ion adsorption by microbial flocculants in synthetic wastewater and their related carbonate formation

Although microbial treatments of heavy metal ions in wastewater have been studied, the removal of these metals through incorporation into carbonate minerals has rarely been reported. To investigate the removal of Fe^3＋ and Pb^2＋, two representative metals in wastewater, through the precipitation of carbonate minerals by a microbial flocculant （MBF） produced by Bacillus mucilaginosus. MBF was added to synthetic wastewater containing different Fe^3＋ and Pb^2＋ concentrations, and the extent of flocculation was analyzed. CO2 was bubbled into the mixture of MBF and Fe^3＋/Pb^2＋ to initiate the reaction. The solid substrates were analyzed via X-ray diffraction, transmission electron microscopy and energy dispersive spectroscopy. The results showed that the removal efficiency decreased and the MBF adsorption capacity for metals increased with increasing heavy metal concentration. In the system containing MBF, metals （Fe^3＋ and Pb^2＋）, and CO2, the concentrated metals adsorbed onto the MBF combined with the dissolved CO2, resulting in oversaturation of metal carbonate minerals to form iron carbonate and lead carbonates. These results may be used in designing a method in which microbes can be utilized to combine CO2 with wastewater heavy metals to form carbonates, with the aim of mitigating environmental problems.     

Formic acid as an alternative reducing agent for the catalytic nitrate reduction in aqueous media

Formic acid was used for the nitrate reduction as a reductant in the presence of Pd:Cu/γ-alumina catalysts. The surface characteristics of the bimetallic catalyst synthesized by wet impregnation were investigated by SEM, TEM-EDS. The metals were not distributed homogeneously on the surface of catalyst, although the total contents of both metals in particles agreed well with the theoretical values. Formic acid decomposition on the catalyst surface, its influence on solution pH and nitrate removal efficacy was investigated. The best removal of nitrate (50 ppm) was obtained under the condition of 0.75 g/L catalyst with Pd:Cu ratio (4:1) and two fold excess of formic acid. Formic acid decay patterns resembled those of nitrate removal, showing a linear relationship between kf (formic acid decay) and k (nitrate removal). Negligible amount of ammonia was detected, and no nitrite was detected, possibly due to buffering effect of bicarbonate that is in situ produced by the decomposition of formic acid, and due to the sustained release of H2 gas.     

SPE-UFLC-MS/MS法测定制药废水中四环素类抗生素

文章建立了利用固相萃取-超快速液相色谱-串联质谱(SPE-UFLC-MS/MS)测定制药废水中四环素类抗生素(土霉素、四环素和金霉素)残留的方法。水样经(30%硫酸锌+20%亚铁氰化钾)溶液作为沉淀剂沉淀蛋白质后,上清液采用Oasis HLB固相萃取柱富集和净化,以(0.1%甲酸溶液+乙腈)为流动相进行梯度洗脱,经Agilent ZORBAX SB C18柱分离后,在串联质谱ES(I+)模式下进行MRM检测。该方法四环素类抗生素检出限(S/N=3时)0.02μg/L,3种目标物在0.010¹.0 mg/L范围内线性关系良好,线性相关系数在0.998 21.0 mg/L范围内线性关系良好,线性相关系数在0.998 2⁰.999 8之间。在0.20、0.40和0.60μg/L添加水平,各组分的回收率在80.8%0.999 8之间。在0.20、0.40和0.60μg/L添加水平,各组分的回收率在80.8%⁹7.2%之间,相对标准偏差在5.31%97.2%之间,相对标准偏差在5.31%⁹.92%之间。该方法可满足制药废水中四环素类抗生素残留检测的要求。     

贯彻落实“大气十条”的环境监测技术需求

2013年9月,国务院发布《大气污染防治行动计划》（以下简称《大气十条》）,捆响了向PM2.5污染宣战的“发令枪”,掀起了以防治大气污染为目标的全社会行动。《大气十条》提出,经过五年努力,使全国空气质量总体改善,重污染天气较大幅度减少;京津冀、长三角、珠三角等区域空气质量明显好转。《大气十条》把解决人民群众最关心、最直接、最现实的PM2.5污染问题作为根本出发点和落脚点,切实维护人民群众身体健康和环境权益。     

磁性多孔陶粒生物膜反应器处理焦化废水的试验研究

以磁性材料为原料,经过特定的工艺处理,对多孔陶瓷进行磁化改性获得磁性多孔载体,并将该载体应用于生物膜反应器中进行焦化废水处理试验。对不同类型的多孔陶粒载体进行对比试验,结果表明:磁性载体生物膜反应器对COD、NH3-N的去除率比普通活性污泥法高出25%³0%,比非载体生物膜反应器高出15%30%,比非载体生物膜反应器高出15%²0%左右。反应器的曝气量为1.5 L/h,曝气时间为10 h/d,温度为2520%左右。反应器的曝气量为1.5 L/h,曝气时间为10 h/d,温度为25³0℃。焦化废水经磁性载体生物膜反应器处理后,上清液中COD,NH3-N的去除率均在90%左右。出水浓度达到国家工业废水排放二级标准(GB18918-2002)。     

我国水泥工业碳排放特征及动态变化分析

水泥工业是温室气体二氧化碳(CO2)的主要排放源,利用碳排放数学模型计算2001-2010年我国水泥工业碳的排放量,分析碳排放量的变化特点和发展趋势。结果表明:水泥工业碳排放总量逐年增长,与水泥产量和排放强度呈线性关系。"十一五"期间单位产品碳排放强度由0.69 t/t下降到0.65 t/t。万元GDP碳排放量2008年达到最低值为0.295 1 t,平均每年万元GDP碳排放量下降2.85%。水泥工业十年间实施节能降耗、资源循环利用、提高经济效益等措施,对于减少碳排放具有明显效果。