地质雷达在监测地下水石油烃污染中的应用

随着我国工业迅速发展,石油烃污染威胁地下水安全问题逐渐暴露出来。地质雷达作为一种非破坏性的原位探测技术在国外已广泛应用于地下水监测,由于石油烃在地质雷达图谱上通常显示出高阻异常特征,这为探测地下水中的石油烃污染提供了可能。简述了地质雷达探测石油烃的原理,探测效果的影响因素,并列举了部分国外实例,证实了地质雷达探测地下水石油烃污染的可行性。     

明胶厂剩余高钙污泥作为燃煤固硫剂的应用研究

明胶生产产业在废水处理工艺中产生大量剩余高钙污泥,采用该剩余污泥作为燃煤固硫剂,在高温管式电阻炉内进行燃烧实验,通过测定燃烧前和燃烧后样品中的硫含量确定该剩余污泥的固硫效果。通过单因素研究煤粉粒径、剩余污泥粒径和剩余污泥/煤样%等影响因素对固硫率的影响。在单因素试验的基础上通过正交设计法优选达到较高固硫率的实验条件。实验结果表明:影响固硫率的因素从大到小依次为燃烧温度>剩余污泥/煤样%>煤粉粒径>剩余污泥粒径。以剩余污泥作为固硫剂,固硫率最高的实验条件为:燃烧温度800℃,剩余污泥/煤样为3%,煤粉粒径60⁹0目,剩余污泥粒径9090目,剩余污泥粒径90¹20目。并且,当温度达到1150℃,煤粉粒径90120目。并且,当温度达到1150℃,煤粉粒径90¹20目,剩余污泥粒径为60120目,剩余污泥粒径为60⁹0目,污泥/煤样(质量比)为3%时,固硫率可达62.78%,说明在高温下该剩余污泥保持较高的固硫率。将明胶厂剩余污泥作为固硫剂是较为合适的再利用方法,可有效缓解当前该污泥大量堆积污染环境的状况。     

Pb(II) removal from water using Fe-coated bamboo charcoal with the assistance of microwaves

Bamboo charcoal(BC) was used as starting material to prepare iron-modified bamboo charcoal(Fe-MBC) by its impregnation in FeCl 3 and HNO 3 solutions simultaneously,followed by microwave heating.The material can be used as an adsorbent for Pb(Ⅱ) contaminants removal in water.The composites were prepared with Fe molar concentration of 0.5,1.0 and 2.0 mol/L and characterized by means of N 2 adsorption-desorption isotherms,X-ray diffraction spectroscopy(XRD),scanning electron microscopy coupled with energy dispersive X-ray spectrometry(SEM-EDS),Fourier transform infrared(FT-IR) and point of zero charge(pH pzc) measurements.Nitrogen adsorption analyses showed that the BET specific surface area and total pore volume increased with iron impregnation.The adsorbent with Fe molar concentration of 2 mol/L(2Fe-MBC) exhibited the highest surface area and produced the best pore structure.The Pb(Ⅱ) adsorption process of 2Fe-MBC and BC were evaluated in batch experiments and 2Fe-MBC showed an excellent adsorption capability for removal Pb(Ⅱ).The adsorption of Pb(Ⅱ) strongly depended on solution pH,with maximum values at pH 5.0.The ionic strength had a significant effect on the adsorption at pH < 6.0.The adsorption isotherms followed the Langmuir isotherm model well,and the maximum adsorption capacity for Pb(Ⅱ) was 200.38 mg/g for 2Fe-MBC.The adsorption processes were well fitted by a pseudo second-order kinetic model.Thermodynamic parameters showed that the adsorption of Pb(Ⅱ) onto Fe-MBC was feasible,spontaneous,and exothermic under the studied conditions,and the ion exchange mechanism played an significant role.These results have important implications for the design of low-cost and effective adsorbents in the removal of Pb(Ⅱ) from wastewater.     

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.     

Removal of Cd2+ from water by Friedel’s salt (FS: 3CaO.Al2O3·CaCl2·10H2O): Sorption characteristics and mechanisms

The development of low-cost and efficient new mineral adsorbents has been a hot topic in recent years. In this study, Friedel’s salt (FS:3CaO·A12O3 ·CaCl2 ·10H2O), a hexagonal layered inorganic absorbent, was synthesized to remove Cd2+ from water. The adsorption process was simulated by Langmuir and Freundlich models. The adsorption mechanism was further analyzed with TEM, XRD, FT-IR analysis and monitoring of metal cations released and solution pH variation. The results indicated the adsorbent FS had an outstanding ability for Cd(Ⅱ) adsorption. The maximum adsorption capacity of the FS for Cd(Ⅱ) removal can reach up to 671.14 mg/g. The nearly equal numbers of Cd2+ adsorbed and Ca2+ released demonstrated that ion-exchange (both surface and inner) of the FS for Cd(Ⅱ) played an important role during the adsorption process. Furthermore, the surface of the FS after adsorption was microscopically disintegrated while the inner lamellar structure was almost unchanged. The behavior of Cd(Ⅱ) adsorption by FS was significantly affected by surface reactions. The mechanisms of Cd2+ adsorption by the FS mainly included surface complexation and surface precipitation. In the present study, the adsorption process was fitted better by the Langmuir isotherm model (R2 = 0.9999) than the Freundlich isotherm model (R2 = 0.8122). Finally, due to the high capacity for ion-exchange on the FS surface, FS is a promising layered inorganic adsorbent for the removal of Cd(Ⅱ) from water.     

Enhanced photocatalytic activity of quantum-dot-sensitized one-dimensionally-ordered ZnO nanorod photocatalyst

An efficient photocatalyst was fabricated by assembling quantum dots （QDs） onto one-dimensionally-ordered ZnO nanorods, and the photocatalytic properties for Methyl Orange degradation were investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, UV-Vis-NIR absorption spectroscopy and photoluminescence. The results indicate that the catalyst with assembled QDs is more favorable for the degradation than the pristine ZnO nanorods. The QDs with core-shell structure lower the photocatalytic ability due to the higher carder transport barrier of the ZnS shell layer. Besides its degradation efficiency, the photocatalyst has several advantages given that the one-dimensionally-ordered ZnO nanorods have been grown directly on indium tin oxide substrates. The article provides a new method to design an effective and easily recyclable photocatalyst.     

Research on the evolvement of morphology of coking coal during the coking process

The evolvement of morphology and structure of the coal with different metamorphic degrees during coking process in the vertical furnace was investigated by infrared Image detector. Moreover, the temperature distribution in the radial direction and the crack formation were also studied in heating process. The results show that the amount of crack and the shrinkage level of char decrease with the coal rank rising. In addition, the initial temperature of crack formation for char increases with the coal rank rising.     

铬(Ⅵ)土著还原菌筛选及初步鉴定实验研究

以重铬酸钾为供试物,用固体平板法和还原实验对铬(Ⅵ)土著还原菌进行筛选,用载片培养法、革兰氏染色法、鞭毛染色法、芽孢染色法对还原菌做初步的鉴定,共筛选出16株铬(Ⅵ)土著还原菌,并挑选出还原率相对较高的Z2(35.2%)、Z3(45.2%)、Z4(38.6%)、X8(30.4%)、X10(29.4%)作为铬(Ⅵ)的优势还原菌株。经初步鉴定,土著真菌Z2为黑曲霉(Aspergillusniger),Z3、Z4为镰刀菌属(Fusariumsp.),土著细菌X8、X10为芽孢杆菌(Bacillussp.)。实验的方法和成果将为铬(Ⅵ)污染土壤微生物治理技术的推广应用提供技术支持。     

生活垃圾中废塑料分选回收技术概述

近年来,废塑料在城市生活垃圾中占有相当大的比例,其含量正呈逐年上涨的趋势,因此对塑料进行分选和资源化利用势在必行。塑料分选技术是摆在我们中间的一项难题,目前生活垃圾废塑料的分选技术五花八门．由于在全国各地废塑料在垃圾中的还水量等因素的影响,现实中能实现废塑料的分选还不成熟。因此,研究一套适合废塑料的分选技术迫在眉睫。     

采掘业井工开采项目地下水环境影响评价相关问题探讨-以凯达煤矿项目为例

本文针对采掘业并工开采项目地下水环境影响评价的特点,根据在环境影响评价工作中的实践经验,以位于内蒙古自治区鄂尔多斯市准格尔旗境内的凯达煤矿为例,就地下水导水裂隙带、地下水影响范围、含水层、居民水井等问题具体分析、并结合产生的影响提出具体的防治措施.