重庆市突发环境事件时空格局及影响研究

基于2009年-2015年重庆市突发环境事件统计数据,研究了重庆市近7年突发环境事件的动态变化趋势、空间分布格局及污染影响特征,讨论了引发突发环境事件内外部因素之间的关系.结果表明:重庆市7年内共发生突发环境事件134起,且呈波动下降趋势,春季和夏季为交通事故和自然灾害高发期;突发环境事件空间上主要集中在主城九区及相邻的区县,渝西、渝东南及渝东北各区县发生次数较少.道路交通事故、设备故障和操作不当是导致突发环境事件的主要因素,主要发生形式为泄漏.污染类型主要为水污染和水气复合污染,污染物出现频率大小为:油类>酸碱类>液氨>苯及其化合物>减水剂>其他各种污染物.     

中国低中放近地表处置场环境评价方法研究

放射性废物的处置是对其管理的最终步骤.放射性废物处置的基本安全目标是保护人类和环境免受电离辐射的有害影响.开展处置场环境影响评价可以量化它对人体健康和环境潜在影响.通过与IAEA近十几年的最新研究成果相比较,分析了中国低中放近地表处置场现行评价方法的不足,提出了改进方式,并对中国近地表处置场环境影响评价技术研究下一步应开展的工作进行了探讨.     

低中放处置场环境评价参数灵敏度分析

选取90Sr、239Pu和14C为代表核素,采用单参数变分法对某低中水平放射性固体废物处置场环境影响评价中与核素迁移相关的主要评价参数开展了参数灵敏度分析.分析结果表明:对于低中放处置场而言,环境影响评价模式中主要评价参数的选择对最终评价结果的影响很大,因此在环境影响评价中开展不确定度及敏感度分析是必要的.     

甘肃合水地区全新世以来土壤剖面黑碳记录及其气候变化

针对甘肃合水马家村(MJC)全新世黄土剖面进行野外采样,分析磁化率和黑碳(焦炭和烟炱)等古气候指标,试图探讨黄土高原北部全新世以来生物质燃烧特征以及自然生态环境演变过程,结果表明:末次冰期和全新世早期(11500—8500 a BP)气候寒冷而干旱,区域野火事件时而发生,植被生物量是此阶段野火发生与蔓延的限制因素;距今8000年以来,黑碳和炭屑浓度整体呈现下降趋势。由于季节性降水增多从而抑制大范围火灾发生几率。然而,8000—7000 a BP和3500—2500 a BP野火频率明显上升,这可能与仰韶时期老官台文化和寺洼文化时期的古人类放火烧荒和开垦农田等活动有关;全新世晚期(3100 a BP至今)气候进一步干旱,生物质燃烧增强与人口增加和人类土地利用水平密切相关,其中1500—1000 a BP出现一次较为明显的峰值,这可能与隋唐以来该区农耕活动加强有关。可见,近2000年以来黄土高原北部地区生物质燃烧特征受到气候和人类活动复合驱动所控制。     

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。     

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.