Separation and Preconcentration of Boron with a Glucamine Modified Novel Magnetic Sorbent     

Bilsen Tural 《洁净——土壤、空气、水》2010,38(4):321-327

A novel, simple method based on magnetic separation was developed for analytical purposes. In this method, N‐methyl‐D‐glucamine (NMDG) modified magnetic microparticles that were synthesized by using the sol‐gel method were used for the selective extraction and preconcentration of boron from aqueous solutions. This method combines the simplicity and selectivity of solvent extraction with the easy separation of magnetic microparticles from a solution with a magnet without any preliminary filtration step. The structure of the prepared γ‐Fe₂O₃‐SiO₂‐NMDG (magnetic sorbent) composites were characterized by using X‐ray diffraction (XRD), Transmission Electron Microscopy (TEM), and Fourier Transform Infrared Spectroscopy (FTIR). The influence of different parameters on the sorbent capacity, such as the sorption/desorption of boron, magnetic sorbent dosage, pH, equilibrium time, type, and amount of stripping solution, were evaluated by using the magnetic sorbent. Any equilibrium pH greater than 6 can be used for sorption. Desorption from the sorbent was carried out by using 1.0 M HCl. The sorption and desorption efficiency of the γ‐Fe₂O₃‐SiO₂‐NMDG was found as 92.5 ± 0.5% and 99.8 ± 6%, respectively.  相似文献   

造礁珊瑚碳、氮、硼同位素的海洋酸化指示意义     

韩韬  余克服  陶士臣 《热带地理》2016,36(1):48-54

大气CO2体积分数升高导致的海洋酸化不仅会降低海水pH,还会改变其碳酸盐平衡体系,使得海水中文石饱和度（Ω）降低,相应地会降低珊瑚钙化的速率。已有研究表明：珊瑚骨骼δ13C、δ11B和δ15N具有记录Suess Effect、生物生产力、海水pH值以及营养源的能力;主要表现为：δ11B记录的pH值、δ13C记录的海水无机碳库（DIC）δ13C和生物生产力,以及δ15N记录的陆源物质输送量相结合,可用来指示受季风影响的南海“大陆架碳泵”和近海污染与海洋酸化的联系。目前关于珊瑚对海洋酸化的记录研究仍相对较少,珊瑚碳-氮-硼同位素组合的应用将会加深对于海洋酸化与气候变率和全球碳、氮循环的关系的认识,可能成为揭示海水pH值变化规律性的重要手段。  相似文献   

济阳县土壤元素有效量及其影响因素研究     

代杰瑞  庞绪贵  曾宪东  王红晋 《山东地质》2009,(10):32-36

通过对济阳县生态地球化学调查研究,该区受成土母质来源、土壤类型、地形地貌及其理化性质等因素影响,土壤元素全量、有效量及有效度表现为：低平洼地土壤中K,P,N,Se,Mn,Fe,Zn,Cu和Mo全量较高,P,N,Se和Cu有效量较高,显示为低平洼地为黏质成分的沉积成因特点;而决口扇形地区土壤Cu,Mo,N,Zn,B有效量和全量均偏低。富含有机质,且pH相对较低的潮土中Se,Cu,Mo和B等元素有效度较高,贫有机质、pH相对较高的草甸风沙土中N,Fe,Cu,Mo,B和S等元素有效量较低,但K有效量和有效度均较高。统计分析表明,土壤中K,P,N,S和Cu等元素全量与有效量间具显著正相关性,表明全量是有效量的重要影响控制因素;有机质含量与K,P,Zn,Cu和B有效度间为显著正相关,说明有机质较高有利于土壤元素活化;Fe,P,S,Zn,B和Cu有效度与pH值为显著负相关,表明土壤酸性增强会增加这类元素的生物有效性。  相似文献   

河南渑池铝土矿成矿区地球化学背景   总被引：3，自引：0，他引：3  

王燕茹 《地质与勘探》2012,48(3):526-532

[摘 要]地球化学元素的分布特征反映了元素矿化富集规律。本文在了解矿床地质背景及地球化学性质的基础上,通过对河南渑池地区水系沉积物地球化学测量数据的统计分析,着重研究铝土矿成矿区的地球化学背景,寻找地球化学找矿指标,希望对以后的勘察工作有所借鉴。研究区的铝土矿带位于石炭系本溪组地层中,且本溪组不整合覆盖于奥陶纪地层之上。与上层地层相比,矿层富含Al₂O₃、高场强元素(HSFS),尤其是硼元素。对水系沉积物地球化学数据进行分析,得出反映元素分布形态的地球化学图,结果表明,只有B 元素可以明确反应铝土矿的空间分布位置。矿床点一般沿硼元素高值区边界分布,表明B 元素可以作为河南渑池铝土矿成矿区的地球化学找矿指标。  相似文献   

粗粒土三轴试验数值模拟与试样颗粒初始架构初探   总被引：4，自引：1，他引：3  

王光进  杨春和  张超  马洪岭  冒海军  侯克鹏 《岩土力学》2011,32(2):585-592

试样颗粒初始架构是粗粒土室内三轴试验中一个难以人为控制的因素。基于元胞自动机方法,结合粗粒土的室内三轴试验开发了能制备不同颗粒初始架构粗粒土试样的HHC-CA模型,该模型制备的粗粒土试样表征了粗粒土各粒组分布的不均匀性和随机性,再借助FLAC3D进行粗粒土三轴数值模拟试验,并探讨了试样剪切带内的砾石含量和试样砾石含量对内摩擦角的影响。数值模拟结果表明,同一粒径级配下,粗粒土的内摩擦角值与剪切带内的砾石含量呈增函数关系;试样砾石含量的增加可能会出现内摩擦角减小的现象,但同一粒径级配下的内摩擦角均值随试样砾石含量的增加而明显增大。  相似文献   

Geology,mineral chemistry and tourmaline B isotopes of the Córrego Bom Sucesso area,southern Serra do Espinhaço,Minas Gerais,Brazil: Implications for Au–Pd–Pt exploration in quartzitic terrain     

Alexandre Raphael Cabral  Bernd Lehmann  Miguel Tupinambá  Michael Wiedenbeck  Michael Brauns 《Journal of Geochemical Exploration》2011

The Palaeo-Mesoproterozoic metasiliciclastic rocks of the southern Serra do Espinhaço, Minas Gerais, Brazil, are host to historically important alluvial deposits of diamonds and gold. Detrital gold grains often comprise Au–Pd–Pt intermetallic compounds, with low Ag contents, which contain inclusions of tourmaline and titaniferous hematite (up to ~ 6 wt.% TiO₂). The latter minerals connect the alluvial mineralisation to the rutile–hematite–quartz veins and tourmalinisation observed in the quartzitic country rocks of the alluvial gravel. The quartzite (Sopa-Brumadinho Formation of lacustrine to fan-deltaic origin) is affected by pervasive B metasomatism with F-bearing tourmaline replacing the recrystallised quartz fabric. The tourmaline belongs to the alkali group, with Mg/(Mg + Fe) and X/(X + Na) ratios in the ranges from 0.5 to 0.7 and 0.18 to 0.29, respectively, where X represents vacancies in the X site. Boron-isotopic values of tourmaline vary from ~ 1 to − 10.4‰ δ¹¹B. The B-isotope range, in conjunction with the Na–Mg-rich tourmaline composition, and the widespread occurrence of tourmalinite in the Sopa-Brumadinho Formation suggest a derivation from non-marine evaporitic brines. Brines are capable of transporting otherwise immobile Ti and explain, under oxidising conditions, the fractionation of Ag from Pd to precipitate palladiferous gold with extremely high Pd/Ag ratios. Zirconium-in-rutile and Ti-in-quartz temperatures for a variety of hematite-rich veins suggest episodic vein emplacement over a temperature range from around 500 °C to ~ 350 °C. Cross-cutting relationships and episodic vein emplacement indicate a late-Brasiliano age.  相似文献   

对正热电离质谱法硼同位素测定的实验设计和条件优化          下载免费PDF全文

魏海珍  肖应凯  孙爱德 《盐湖研究》2003,11(1):26-30

为了确定正热电离质谱法测定硼同位素时的最佳实验条件 ,采用均匀设计法进行实验表头设计 ,并用MATLAB进行数据处理和回归模型优化。将最佳优化条件应用于硼同位素测定中 ,得到了与理论计算相吻合的高精度测定结果。  相似文献   

Boron substitution in diopside evaluated through 11B nuclear reaction analysis     

U. Hålenius  P. Kristiansson  H. Skogby 《Physics and Chemistry of Minerals》2000,27(10):681-688

 Nuclear reaction analyses on boron in flux-grown Me³⁺- and Na⁺-doped diopside crystals utilising the ¹¹B(p,2α)⁴He reaction in conjunction with EMP analyses for major elements and optical absorption spectroscopy for determination of Me-valence state distributions show that appreciable amounts of B may enter the diopside lattice in crystals produced in Na₂B₄O₇ fluxes. The results indicate that the substitution ^[6]Me^3+[4]B^3+[6]Mg²⁺ ₋₁ ^[4]Si⁴⁺ ₋₁ operates in the present diopside samples in addition to the coupled substitution ^[6]Me^3+[8]Na^+[6]Mg²⁺ ₋₁ ^[8]Ca²⁺ ₋₁. The specific NRA technique applied allows for quantitative, high resolution (ca. 5 μm) B analyses at ppm level as well as high-resolution and high-contrast imaging of B-concentration patterns in minerals. The estimated detection limit and relative error of the B analyses are 10 ppm and 5–10%, respectively. Received: 20 September 1999 / Accepted: 6 June 2000  相似文献   

Chemical and boron isotopic compositions of tourmaline from the Paleoproterozoic Houxianyu borate deposit,NE China: Implications for the origin of borate deposit     

《Journal of Asian Earth Sciences》2014

The Houxianyu borate deposit in northeastern China is one of the largest boron sources of China, hosted mainly in the Paleoproterozoic meta-volcanic and sedimentary rocks (known as the Liaohe Group) that are characterized by high boron concentrations. The borate ore-body has intimate spatial relationship with the Mg-rich carbonates/silicates of the Group, with fine-grained gneisses (meta-felsic volcanic rocks) as main country rocks. The presence of abundant tourmalinites and tourmaline-rich quartz veins in the borate orebody provides an opportunity to study the origin of boron, the nature of ore-forming fluids, and possible mineralization mechanism. We report the chemical and boron isotopic compositions of tourmalines from the tourmaline-rich rocks in the borate deposit and from the tourmaline-bearing fine-grained gneisses.Tourmalines from the fine-grained gneisses are chemically homogeneous, showing relatively high Fe and Na and low Mg, with δ¹¹B values in a narrow range from +1.22‰ to +2.63‰. Tourmalines from the tourmaline-rich rocks, however, commonly show compositional zoning, with an irregular detrital core and a euhedral overgrowth, and have significantly higher Mg, REE (and more pronounced positive Eu anomalies), V (229–1852 ppm) and Sr (208–1191 ppm) than those from the fine-grained gneisses. They show varied B isotope values ranging from +4.51‰ to +12.43‰, which plot intermediate between those of the terrigenous sediments and arc rocks with low boron isotope values (as represented by the δ¹¹B = +1.22‰ to +2.63‰ of the fine-grained gneisses of this study) and those of marine carbonates and evaporates with high boron isotope values. In addition, the rim of the zoned tourmaline shows notably higher Mg, Ti, V, Sn, and Pb, and REE (particularly LREEs), but lower Fe, Co, Cr, Ni, Zn, Mn, and lower δ¹¹B values than the core. These data suggest that (1) the sources of boron of the borate ore-body are mainly the Paleoproterozoic meta-volcanic and sedimentary rocks, and (2) the ore-forming fluids should be the high temperature metamorphic fluids related to the amphibolite-facies metamorphism of the Paleoproterozoic foldbelt, which leach boron from the boron-rich meta-volcanic and sedimentary rocks of the Liaohe Group, and the boron-rich metamorphic fluids subsequently interacted with the marine Mg-rich carbonates and evaporates, forming borate deposit, the tourmaline overgrowth in the rim and the tourmaline-rich rocks.  相似文献   

Identification of the origin of salinization in groundwater using multivariate statistical analysis and geochemical modeling: a case study of Kaohsiung,Southwest Taiwan     

Hsueh-Yu Lu  Tsung-Ren Peng  Tai-Sheng Liou 《Environmental Geology》2008,55(2):339-352

The study of brine aquifers in southern Taiwan is highly complicated by hybrid geochemical reactions, which obscure important geochemical information. Using multivariate analysis on major and minor ion compositions normalized by Cl⁻ content, chemical constituents were combined into two principal components representing brine mixing and mineral precipitation. Comparing to multivariate analysis on the original data, this procedure reveals more geochemical information. It demonstrates that the brine groundwater of the region is primarily composed of highly evaporated seawater. The evaporation ratio is >70%; a point at which calcite, dolomite and gypsum precipitate. Oxygen and hydrogen isotopic compositions confirm this inference; and further, geochemical modeling quantitatively determined the evaporation ratio to be about 85%. Natural boron contamination is a consequence of brine groundwater. Two evolutionary trends in the plotting of the Cl/B ratio versus Cl⁻ can be identified: (1) Cl/B ratio decreases with boron being released from clay minerals when brine aquifers are flushed with freshwater; and (2) Cl/B ratio increases when seawater of a high Cl/B ratio infiltrates coastal aquifers.  相似文献