双层内衬改造技术在埋地油罐中的应用研究

介绍了共结构双层内衬改造技术,其结构共由5层组成,分别为基础层(防腐层和加强密封层组成)、中空监测层、内衬加强层、防油防腐层和导静电层;采用该技术可对加油站埋地单层钢制油罐进行双层改造,经过罐内清洗、喷砂除锈、基础层施工、中空监测层施工、内衬加强层施工、防油防腐层施工、导静电层施工和整个系统气密性的保压检测,完成双层内衬油罐的现场改造;采用GB30040规定的Ⅰ级真空泄漏监测方法,可以在油品泄漏前报警,实现埋地油罐整体安全水平的提升,具有重要的现实意义。     

遂宁市主城区环境空气质量现状及原因分析研究

利用遂宁市2017年1月份4个国控环境空气自动监测数据,分析了遂宁市主城区环境空气质量现状,与整个成渝地区和周边城市的空气质量进行了横向比较,并阐述了遂宁市空气质量变化的原因.结果发现遂宁市主城区2017年1月份空气质量指数的范围为32～203,优良率为54.8％,首要污染物为PM2.5,空气质量同比下降了22.8％,环比下降了26.1％,但均显著优于成渝地区和周边城市的平均水平,并从4个方面阐述了空气质量下降的原因.最后,根据遂宁市大气污染现状,提出了4条针对性的防治措施.     

郑州市城市生态环境变化研究

随着城市化的发展,城市生态环境变化较大.基于遥感技术,利用遥感生态指数对郑州市城市生态环境变化进行评价与检测,以对城市规划建设提供科学依据,从而促进城市健康可持续发展.结果表明:2006年-2017年,郑州市生态环境质量呈下降趋势,其中绿度指标与干度指标对城市生态环境的影响最大;郑州市生态环境变好的区域占18.43%,生态环境变差的区域占42.54%,变差的区域主要为新建成区,这些区域应是今后生态环境改善的重点区域.     

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。     

因子分析在黄河上游干流地区滑坡灾害中的应用

黄河上游地区干流滑坡灾害频繁发生,造成了严重的经济损失和人员伤亡。对该区滑坡灾害进行研究,对于指导该区的抗灾、减灾和预防工作意义重大。采用遥感技术和野外采样实测,获取了研究区的129处滑坡灾害数据,进而对滑坡灾害影响因素进行了因子分析。通过因子分析,得到公因子,并对公因子命名。在此基础上,计算了因子得分及综合得分,并对其进行了排序。研究结果表明:灾害数据变量之间有较强的相关性,滑坡发生主要受到滑体标高因子、滑体外形因子、地表因子、环境因子和滑体性质5个公共因子的影响。滑体标高、环境特征和滑体性质对滑坡的影响较大,滑体外形因素和地表因素对滑坡发生的影响相对较小。     

用氯和氢氧同位素揭示洋戴河平原地下水的形成演化规律

通过分析地表水和地下水中氯离子浓度和δD、δ¹⁸O值的空间分布特征,揭示了秦皇岛洋戴河平原地下水的形成演化规律.结果发现,洋戴河平原地表河水来源于中上游水库水和大气降水的混合,且河水沿程受到δD、δ¹⁸O值、氯离子浓度更低的支流或灌渠水补给,从而使δD、δ¹⁸O值、氯离子浓度呈现沿程逐渐降低的现象.山前丘陵区地下水主要接受大气降水的直接补给,洪积扇及山麓地带地下水受到了一定的蒸发作用影响,除了接受丘陵区地下水的侧向补给外,洋河附近地下水还受到洋河水库水的混合.研究区西部咸水带的地下水由上游地下水和大泥河地热咸水混合而成,地热咸水的混合比率约为13%,而东部咸水带的地下水由上游地下水、本地污水和地热咸水混合而成,地热咸水的混合比率不超过9%.在海水入侵区,地下水主要由本区地下淡水和海水(海水混合比率不超过10%)混合而成,并且受到了不同程度的地表水或农田灌溉水的补给,其中,浦河一带是地表水或灌溉水补给较为明显的地段.     

流化床O2/CO2气氛下添加SiO2对燃煤PM2.5的控制

采用小型流化床研究了在O2/CO2气氛下添加SiO2对PM2.5(空气动力学直径小于2.5 μm的颗粒物)的控制,试验在1123 K、O2/CO2气氛下进行,并采用荷电低压撞击器(ELPI)采集和分析燃烧后的PM2.5.结果表明,添加SiO2是燃烧过程中影响PM2.5生成的重要因素.添加SiO2后,生成PM1的质量浓度均降低,而PM1-2.5的质量浓度均略有增加;PM2.5质量粒径分布均呈双峰分布,峰值分别出现在0.2 μm和2.0μm左右.随着SiO2添加量的增加,PM2.5中的S、K、Na、Cu和Pb元素的含量呈减少的趋势;随着颗粒粒径减小,S、K、Na、Cu和Pb元素的含量有增高的趋势.     

土壤镉污染的现状及修复研究进展

镉是一种对人类和动物健康危害严重的重金属。土壤镉污染问题已经成为全球研究热点。重点分析了镉污染土壤中镉的来源,镉对动植物、人体的危害,并提出了对镉污染土壤的修复的方法。     

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.     

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.