酿酒酵母吸附Pb(Ⅱ)的表面特性研究

为深入探讨酿酒酵母吸附Pb（Ⅱ）的微观作用机制,本文利用表面显微分析技术（SEM-EDS、TEM-EDS、AFM）研究了酿酒酵母细胞吸附重金属离子Pb（Ⅱ）前后的细胞表面变化.研究结果表明,酿酒酵母细胞与Pb（Ⅱ）作用后,细胞表面除吸附Pb（Ⅱ）外,同时产生大量更高浓度的含Pb（Ⅱ）沉淀,导致Pb（Ⅱ）从溶液中被去除.酵母与Pb（Ⅱ）反应前,酵母细胞表面可检测到的主要元素包括C、O、N、P、S、K、Mg;酵母与Pb（Ⅱ）作用后,细胞表面始终保持C、O、P吸收峰,而N、K、Mg、S吸收峰随反应条件不同而减弱、消失或增强.P作为细胞表面组分可能与Pb（Ⅱ）结合.酵母与Pb（Ⅱ）作用过程中,重金属离子促进酵母细胞释放细胞内含物.原子力显微镜（AFM）证实,云母片表面对酵母吸附Pb（Ⅱ）后细胞的铺展变形作用明显增大.     

脱水污泥等温干燥特性实验研究及回归分析

利用热重差热分析仪（DTG）对脱水污泥进行干燥实验,测定干燥参数和干燥条件对脱水污泥等温干燥特性的影响,研究了3个温度水平（85℃,100℃,120℃）,5个空气流速（10mL/min,20mL/min,40mL/min,50mL/min,70mL/min）和3个升温速率（15℃/min,20℃/min,40℃/min）。结果表明,样品的干燥速率随着终温的升高、升温速率和空气流速的增大而加快。脱水污泥的干燥过程主要分为加速、恒速和降速3个阶段,且降速干燥段在整个干燥过程中所占的比例较大。其干燥数学模型符合Page方程,经拟合得到 。验证表明,拟合方程算得的MR值与实验结果比较接近。该模型方程可用于描述城市污水污泥的干燥。     

南方重金属矿区重金属的污染特征及评价

 采用全面踏查和典型调查相结合的方法,对福建主要重金属矿区的尤溪铅锌矿、连城铅锌矿和连城锰矿不同片区重金属污染状况进行调查。结果表明：福建重金属矿区重金属污染极其严重,矿区中Mn、Zn、Pb、Cd最高含量分别达92 546、27 454、23 792和248 mg/kg,是对照区的几倍至上百倍。根据国家土壤环境质量三级标准,按照重金属单项污染指数标准进行的污染评价表明：南方重金属矿区Zn、Pb、Cd均达到重度污染标准,污染程度表现为尤溪铅锌矿区>连城铅锌矿区>连城锰矿区。按照综合污染指数评价标准,福建连城铅锌矿、连城锰矿和尤溪铅锌矿的综合污染指数也达到重度污染标准,分别是重度污染临界标准的16.5、10.6和53.6倍,不同矿区的重金属污染程度大小排序为尤溪铅锌矿区>连城铅锌矿区>连城锰矿矿区。     

1株脱氮除磷菌的筛选及其特性研究

采用YG培养基,结合蓝白斑筛选、异染粒染色及好氧除磷能力检测等实验,从城市生活污水处理厂好氧生化池的活性污泥中分离出7株好氧除磷菌;再经硝酸盐还原产气和缺氧培养实验,筛选出1株高效脱氮除磷菌;通过16S rRNA基因同源性比较和生理生化鉴定,初步将其鉴定为Pseudomonas grimontii,命名为C18.菌株C18在好氧培养24h后,培养基中上清液磷浓度从38.7mg/L降低到2.28mg/L,除磷率达94.1%.C18在缺氧培养24h后,培养基中上清液磷浓度从44.5mg/L降低到5.21mg/L,除磷率达88.3%;上清液硝酸盐氮浓度从184.2mg/L降低到30.6mg/L,脱氮率达83.4%.菌株C18最适脱氮除磷温度为30℃;最适脱氮除磷pH为7.5.     

三峡库区悬移质泥沙对磷污染物的吸附解吸特性

就三峡库区悬移质泥沙对磷污染物的吸附解吸特性从野外同步监测和室内试验研究两个方面展开研究。选取长江干流、嘉陵江和乌江共7个监测断面于2002年和2003进行野外同步监测,测试结果表明：水中的悬移质泥沙对水中各种覆存形态的磷污染物浓度具有显著影响,单位重量泥沙对磷的吸附量与水体总泥沙含量、泥沙粒径有密切关系。采集寸滩断面泥沙对磷酸盐吸附解吸特性进行室内试验研究,并根据Langmuir吸附动力学方程对吸附解吸过程进行了拟合,发现吸附速率常数k随着泥沙粒径的增加而呈递增变化,而磷酸盐初始浓度对k值的影响并不明显,同时,磷酸盐解吸量随着泥沙浓度的增加和粒径的增加呈递减变化,k值随着泥沙粒径的增加而呈递增变化,泥沙浓度对k值的影响不明显。     

生物活性炭去除水中挥发性苯系物的基础研究

采用连续流生物活性炭(BAC)工艺处理水中挥发性苯系物(BTEX,包括苯、甲苯、乙苯、二甲苯),评价进水负荷、活性炭炭型等因素对于BAC处理性能的影响.研究表明,在40d的处理时间内,除苯之外,其余BTEX的BAC出水中均未检出苯系物(进水为6mg/L).为了检验BAC在高BTEX负荷情况时的处理效果,将进水浓度设定为19~32mg/L左右,在EBCT为1.2min条件下同样只有苯的出水浓度上升至10mg/L(C/Cin为0.45),然后略有下降,最终保持在5~10mg/L(C/Cin为0.3以下),其余苯系物出水浓度均一直保持小于5mg/L.这表明BAC可以有效地处理高负荷BTEX(8.68~12.9kgTOC/(m3·d))的进水.生物活性炭对于活性炭吸附容量的恢复有比较明显的作用,煤质炭和椰壳炭的生物再生效率分别为53.6%和26.6%,煤质炭再生效率高的原因可能是其具备更多的大型中孔和大孔.     

220kV变压器噪声及其传播特性浅析

变压器噪声呈中低频特性,距离衰减率低,传播影响范围大。通过对上海某220kV露天变电站变压器噪声的实测数据进行简要分析,论述了220kV变压器噪声的强度及其频率特性,并探讨了变压器噪声在不同距离范围内的传播衰减特性。     

Removal of copper ions from aqueous solution by calcium alginate immobilized kaolin

Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized kaolin (kaolin/CA), was prepared using a sol-gel method. The e ects of contact time, pH, adsorbent dose, and temperature on Cu2+ adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum Cu2+ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction was a spontaneous and endothermic process.     

Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous silicates hybrid materials

Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water. A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment.     

Removal of heavy metal ions from aqueous solution using red loess as an adsorbent

The adsorption behaviors of heavy metals onto novel low-cost adsorbent, red loess, were investigated. Red loess was characterized by X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectra. The results indicated that red loess mainly consisted of silicate, ferric and aluminum oxides. Solution pH, adsorbent dosage, initial metal concentration, contact time and temperature significantly influenced the efficiency of heavy metals removal. The adsorption reached equilibrium at 4 hr, and the experimental equilibrium data were fitted to Langmuir monolayer adsorption model. The adsorption of Cu(II) and Zn(II) onto red loess was endothermic, while the adsorption of Pb(II) was exothermic. The maximum adsorption capacities of red loess for Pb(II), Cu(II) and Zn(II) were estimated to be 113.6, 34.2 and 17.5 mg/g, respectively at 25°C and pH 6. The maximum removal efficiencies were 100% for Pb(II) at pH 7, 100% for Cu(II) at pH 8, and 80% for Zn(II) at pH 8. The used adsorbents were readily regenerated using dilute HC1 solution, indicating that red loess has a high reusability. All the above results demonstrated that red loess could be used as a possible alternative low-cost adsorbent for the removal of heavy metals from aqueous solution.