Adsorption characteristics of copper ion on nanoporous silica     

Yanhui Niu  Wenbin Yu  Zonghua Qin  Xin Nie  Shuguang Yang  Quan Wan 《Acta Geochimica》2019,(4):517-529

Adsorption by nanoporous media is critically involved in many fundamental geological and geochemical processes including chemical weathering,element migration and enrichment,environmental pollution,etc.Yet,the adsorption behavior of metal ions on nanoporous materials has not been systematically investigated.In this study,MCM-41 material with a monodisperse pore size(4.4 nm)and a large BET specific surface area(839 m^2/g)was hydrothermally prepared and used as a model silica adsorbent to study the adsorption characteristics of Cu^2+as a representative metal ion.The Cu^2+adsorption capacity was found to increase with increasing suspension pH in the range from 3 to 5 and to decrease in the presence of NaNO3.At 25℃,pH=5,and a solid-to-liquid ratio of 5 g/L,the adsorption capacity was determined to be 0.29 mg/g,which can be converted to a dimensionless partition coefficient of 45,indicating a strong enriching effect of nanoporous silica.The adsorption isotherm and kinetic data were fitted to several commonly used thermodynamic,kinetic,and diffusion models.The adsorption mechanism was also studied by Fourier transform infrared spectroscopy,X-ray photoelectron spectroscopy and synchrotron-based X-ray absorption spectroscopy.The results suggest that Cu2+ion adsorption is an entropy-driven endothermal process,possibly involving both outer-sphere and inner-sphere complexes.  相似文献   

南大洋普里兹湾沉积物中生物硅的溶解度研究          下载免费PDF全文

扈传昱  孙维萍沈忱 张海生 《极地研究》2012,24(4):339-345

本文利用中国南极科学考察航次获得的沉积物样品,采用分批（batch）实验方法,获取实验室生物硅溶解度,并结合间隙水中可溶性硅剖面,对普里兹湾沉积物中生物硅的溶出过程进行了初步研究。研究结果如下：在25℃,pH 8条件下,普里兹湾IV-10、 IS-4站表层沉积物中生物硅的实验室溶解度分别为1936、1539μmol/dm3,不同层次沉积物溶出结果显示随深度增加溶解度值降低。根据实验室溶解度数据与间隙水硅酸盐Cd的分析比较,表明研究站位沉积物生物硅的早期成岩过程中生物硅的溶出还伴随有其他化学过程。  相似文献   

硅灰加固宁波软土的试验研究     

王泽平  王常明  江南  张在恒 《岩土工程技术》2020,(2):111-116,121

为探索硅灰对软土的力学性质的影响,以宁波鄞州地区一种淤泥质黏土为试样,掺入不同量的硅灰,对硅灰加固土的力学性质和结构特征进行了测试。采用三轴不固结不排水剪切试验,测试分析了不同掺入量的硅灰加固土的应力应变关系,通过扫描电镜SEM照片分析了不同硅灰掺入量的硅灰加固土的结构特征。结果表明:(1)硅灰可以提高软土的黏聚力,黏聚力随着硅灰掺入量的增加而增大;(2)随着硅灰掺入量的增加,硅灰加固土的抗变形能力呈先增加后减小的趋势;(3)同一围压条件下,随着硅灰掺入量的增加,硅灰加固土的破坏偏应力逐渐增加;(4)随着硅灰掺入量的增加,硅灰加固土中大孔隙逐渐减少,小孔隙逐渐数量增加,孔径<1μm的小孔隙组分逐渐占优。  相似文献   

福建北部近岸东台山岛火山岩形成时代、地球化学与古太平洋板块俯冲的响应          下载免费PDF全文

王飞飞  张勇  韩宗珠  宋维宇  吴浩  宁泽 《中国地质》2020,47(5):1426-1437

福建北部沿岸岛屿岩石组合以晚中生代火成岩为主,研究认为是古太平洋俯冲消减的产物,对反演洋盆构造演化具有重要的指示意义。本次对其中的福建北部海域东台山岛上广泛发育的酸性火山岩进行了锆石U-Pb定年以及全岩主微量地球化学分析工作。2件年代学样品分别获得了92 Ma和86 Ma的锆石U-Pb年龄,确定东台山岛火山岩形成于晚白垩世。全岩地球化学特征指示火山岩样品以酸性钙碱性岩石为主,整体富集Rb、Ba等元素,亏损Nb、Ta、Sr、Eu等元素,显示弧型岩浆岩的地球化学组成。研究认为东台山岛火山岩起源于古老下地壳变沉积岩熔融,并在浅层岩浆房内经历了不同程度的结晶分异过程。结合区域上晚中生代岩浆作用由陆向海的时空迁移特征,福建北部沿岸岛屿火山岩形成的深部动力学机制应该与古太平洋俯冲过程中的板片回转过程相关。  相似文献   

The silica supersaturated waters of northern Evia and eastern central Greece     

G. Stamatis  E. Gartzos 《水文研究》1999,13(17):2833-2845

The area of north Evia and eastern central Greece is characterized by strong geomorphological contrast and is built up mainly of consolidated rocks. Unconsolidated young sediments of Pleistocene to Holocene age cover the valley and basin flats, forming the most productive aquifers in this area. However, two more types of aquifers can be distinguished within the consolidated rock area. The first one is associated with karstified limestones and the second with strongly tectonized ultramafic rocks. The schist–chert formation, with intercalations of shales and cherts, seals the ultramafic masses underneath. Surface and spring waters associated with ultramafic rocks in north Evia and eastern central Greece were studied. Two types of water can be distinguished: (1) high Mg²⁺ and SiO₂ , bicarbonate as the dominant anion, pH 7·4–9·2, temperature 9·5–16·3 °C, low TDS (total dissolved solutes) (459–1037 mg/l), found both in peridotite and serpentinite areas, classified as Mg–HCO₃ type; (2) high Ca²⁺, low Mg²⁺ and SiO₂ , hydroxyl ion as the major anion, pH 11·2, temperature 28 °C, very low TDS (122 mg/l), found in peridotite areas, classified as Ca–OH type. The studied waters are highly supersaturated with respect to quartz, amorphous silica, brucite and most low temperature magnesium silicates (antigorite, sepiolite, talc, etc.). These waters show relatively narrow SiO₂ concentration ranges and a trend parallel to the amorphous silica saturation surface. The silica supersaturated waters have the potential to precipitate silica and consequently could affect the people of the local communities that use it as drinking water, causing health problems (kidney stones). Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

海洋沉积物32 Si测年方法研究     

詹晓青  李超  贾磊  张金鹏  刘广山 《海洋学报》2019,41(2):63-74

天然32Si是宇宙射线成因的，随着降水进入湖泊或海洋，被硅质生物摄取后最终存在于生物硅中。32Si来源单一，生产速率相对恒定，半衰期为150 a，可测年的时间尺度为100~1 000 a，是该时间尺度最合适的测年核素，填补了百年到千年时间尺度测年方法的空白。本文建立了海洋沉积物32Si的测量方法，主要步骤为:（1）样品前处理；（2）生物硅的分离与纯化；（3）生物硅样品中磷的分离与纯化；（4）32P的制样与β计数测量。全程通过硅钼蓝和磷钼蓝分光光度法监测实验过程硅和磷的损失情况，对南沙海域采集的沉积物岩心进行研究，得到南沙海域沉积物岩心32Si的平均活度为16.60 mBq/kg，范围值为8.39~33.34 mBq/kg；32Si在SiO₂中的平均比活度为0.356 Bq/kg，32Si的核素丰度平均值为1.29×10-16（32Si/SiO₂）；根据岩心32Si活度估算得深水区（水深1 335~1 537 m）和浅水区（121~141 m）岩心的沉积速率分别为0.106 cm/a、0.191 cm/a；根据32Si活度计算32Si的平均沉降通量为2.14×10-6 Bq/（cm2·a），与参考文献的结果较为吻合。  相似文献   

二氧化碳注入煤层多用途研究   总被引：1，自引：0，他引：1  

陈润  秦勇  申建  王国玲  刘国伟 《煤田地质与勘探》2008,36(6)

为了减轻环境污染,提高煤层气产率,增加能源储备,根据煤层气地质学和生物气的基本理论,提出二氧化碳(CO2)注入煤层多种用途这一新观点。研究结果显示:煤对CO2具有很强的吸附能力,可将煤层作为CO2的储集层;煤具有优先吸附CO2而滞后吸附甲烷(CH4)的特性,向煤层注入CO2可大大提高煤层气的采收率;产甲烷菌具有利用CO2生成CH4的能力,新生成的CH4成为能源储备的有益补充。可见,CO2注入煤层不仅可有效减少温室气体的排放,强化煤层甲烷产出,而且为新能源生物CH4的生成提供了基质。  相似文献   

Exchange of Short-Chain Oxygenated Volatile Organic Compounds (VOCs) between Plants and the Atmosphere: A Compilation of Field and Laboratory Studies     

J. Kesselmeier 《Journal of Atmospheric Chemistry》2001,39(3):219-233

Field and laboratory investigations of the exchange of the short-chain organic acids – formic acid and acetic acid – as well as their homologous aldehydes are discussed. Both acids are substantially released from several plant species. Emission measurements under field conditions are compiled to give an overview of three years of measurements. Emission rates from several tree species were found in the range between zero and 60 nmoles m^–2 min^–1 for acetic acid and between zero and 90 nmoles m^–2 min^–1 for formic acid though also a deposition has been observed to orange trees. Investigations under laboratory conditions showed an order of magnitude lower emission rates with significant differences under light and dark conditions, and a deposition was observed under certain conditions. Hence, low emission rates or even a bi-directional exchange, emission as well as deposition have to be taken into account. Further differences between field and laboratory studies are discussed considering age of trees, stress effects and a potential production of acids by photochemical conversion of precursors inside enclosures during sampling. Field data on the exchange of form- and acetaldehyde show a complex behavior. We found emission as well as uptake. The bi-directional exchange is significantly triggered by the ambient mixing ratios of both aldehyde species and exhibits a compensation point. Further studies are needed for generalization of the exchange of these and potentially also for other compounds.  相似文献   

Ambient biogenic hydrocarbons and isoprene emissions from a mixed deciduous forest     

J. D. Fuentes  D. Wang  H. H. Neumann  T. J. Gillespie  G. Den Hartog  T. F. Dann 《Journal of Atmospheric Chemistry》1996,25(1):67-95

Experiments were conducted during the growing season of 1993 at a mixed deciduous forest in southern Ontario, Canada to investigate the atmospheric abundance of hydrocarbons from phytogenic origins, and to measure emission rates from foliage of deciduous trees. The most abundant phytogenic chemical species found in the ambient air were isoprene and the monoterpenes -pinene and -pinene. Prior to leaf-bud break during spring, ambient hydrocarbon mixing ratios above the forest remained barely above instrument detection limit (20 parts per trillion), but they became abundant during the latter part of the growing season. Peak isoprene mixing ratios reached nearly 10 parts per billion (ppbv) during mid-growing season while maximum monoterpene mixing ratios were close to 2 ppbv. Both isoprene and monoterpene mixing ratios exhibited marked diurnal variations. Typical isoprene mixing ratios were highest during mid-afternoon and were lowest during nighttime. Peak isoprene mixing ratios coincided with maximum canopy temperature. The diurnal pattern of ambient isoprene mixing ratio was closely linked to the local emissions from foliage. Isoprene emission rates from foliage were measured by enclosing branches of trees inside environment-controlled cuvette systems and measuring the gas mixing ratio difference between cuvette inlet and outlet airstream. Isoprene emissions depended on tree species, foliage ontogeny, and environmental factors such as foliage temperature and intercepted photosynthetically active radiation (PAR). For instance, young (<1 month old) aspen leaves released approximately 80 times less isoprene than mature (>3 months old) leaves. During the latter part of the growing season the amount of carbon released back to the atmosphere as isoprene by big-tooth and trembling aspen leaves accounted for approximately 2% of the photosynthetically fixed carbon. Significant isoprene mixing ratio gradients existed between the forest crown and at twice canopy height above the ground. The gradient diffusion approach coupled with similarity theory was used to estimate canopy isoprene flux densities. These canopy fluxes compared favorably with values obtained from a multilayered canopy model that utilized locally measured plant microclimate, biomass distribution and leaf isoprene emission rate data. Modeled isoprene fluxes were approximately 30% higher compared to measured fluxes. Further comparisons between measured and modeled canopy biogenic hydrocarbon flux densities are required to assess uncertainties in modeling systems that provide inventories of biogenic hydrocarbons.  相似文献   

Precise and Accurate Doping of Nanoporous Silica Gel for the Synthesis of Trace Element Microanalytical Reference Materials          下载免费PDF全文

William O. Nachlas 《Geostandards and Geoanalytical Research》2016,40(4):505-516

This study presents an experimental procedure to fabricate high‐purity silica glass containing a selected element at a specified mass fraction. The procedure was used to prepare glasses doped with trace‐level mass fractions of Ti with the goal of improving analytical confidence when measuring trace elements in quartz. Systematic tests were performed to determine the ideal conditions and procedures for doping nanoporous silica gel with the highest efficiency of dopant recovery. Silica gel was cleaned in concentrated HCl, immersed in a non‐polar doping medium at a controlled pH and doped with precise quantities of ICP‐MS standard solution. Using liquids composed of longer chain molecules as the doping medium diminishes recovery, suggesting that large molecules could obstruct nanopores to inhibit capillary uptake of the dopant. A control experiment using crystalline quartz reinforced the effectiveness of nanoporous silica gel for doping with trace‐level precision. Layered aggregates of silica gel doped with different Ti mass fractions were hot‐pressed to create multi‐layered reference materials that were analysed with multiple techniques at a variety of spatial scales. Analyses at the intra‐grain scale (cathodoluminescence scanning electron microscopy, electron probe microanalysis), at the single grain scale (SIMS), at the sample layer scale (EPMA, laser ablation‐ICP‐MS) and at the bulk scale (ICP‐OES) demonstrated acceptable homogeneity at sample volumes characteristic of most microanalysis techniques and show that nanoporous silica gel holds promise as a highly retentive doping substrate for preparing reference materials for laser‐, electron‐ and ion‐beam microanalysis.  相似文献