红柳沟北镁铁-超镁铁质岩体矿物学特征及矿石成因分析

红柳沟北镁铁-超镁铁质岩体位于柴达木陆块北部的欧龙布鲁克微陆块东北缘,呈岩墙状,出露面积约0.1km~2,由方辉橄榄岩、橄榄二辉岩、含长单辉橄榄岩、橄榄辉长苏长岩、暗色橄榄辉长岩、苏长岩、辉长岩等组成,各岩相带在空间上呈渐变过渡关系。电子探针分析结果显示,岩体的主要造岩矿物为贵橄榄石、古铜辉石、普通辉石和斜长石,并且各矿物的结晶温度为1 307~1 122℃。岩体钛铁矿化明显,主要金属矿物为钛铁矿、钛磁铁矿和磁铁矿。利用橄榄石Fo最高值反演出原生岩浆MgO含量为8.49%,FeO含量为10.03%,TiO_2含量为1.63%,为普通玄武质岩浆。通过综合研究各矿物形成的温度和氧逸度条件,认为岩浆从橄榄石结晶到普通辉石结晶,其氧逸度是缓慢升高的,并且氧逸度是控制红柳沟北岩体Ti-Fe氧化物结晶的主要因素。     

陕西白河县月儿潭绿松石与次生磷钙铝矾研究

对陕西省白河县月儿潭风化严重的绿松石样品进行了岩石薄片观察、化学成分测试、X射线粉晶衍射和红外吸收光谱分析等研究.结果表明,绿松石风化分解由天蓝色退色成黄绿色,最后变成白色,结构也由致密细腻变得松散多孔,主要原因是发生了硫酸根对磷酸根的交代作用,最终的交代产物主要是磷钙铝矾.     

南黄海沉积物中活性铁氧化物对有机碳的保存作用

土壤和沉积物中活性铁对有机质的吸附对有机质具有长期稳定和保存作用,从而在地质时间尺度上缓冲大气CO₂浓度。本文利用连二亚硫酸钠还原性溶解提取活性铁氧化物（FeR）及与之结合的有机碳（Fe-OC）,定量研究了南黄海沉积物中FeR与OC之间的结合方式以及FeR对OC的保存作用,讨论了深度增加对二者相互作用的影响。结果表明,南黄海沉积物中Fe-OC占沉积物总有机碳的份数（f_Fe-OC）为（13.2±7.47）%,即活性铁对OC的年吸附量为0.72 Mt,占全球边缘海沉积物TOC年埋藏通量的0.44%。Fe-OC的平均OC:Fe为4.50±2.61,表明共沉淀作用对有机质的保存起重要作用,且其比值随海源有机质含量增加而增加。Fe-OC稳定碳同位素（δ13C_Fe-OC）结果表明,FeR优先保存活性有机质,但这种选择性随OC:Fe增大而减弱。随深度增加,f_Fe-OC和δ13C_Fe-OC均未表现出显著变化,这与该海域沉积物中有机质活性较低、铁还原作用较弱有关。     

滇池水中铝的形态分布初探

采用铬天青S光度法对滇池水中的总铝和各主要形态铝进行分析，并利用简单易行的紫外吸收表征水中有机物污染程度和颗粒物含量，初步探讨了各因素的变化对铝形态分布的影响。     

柱撑蛭石吸附去除废水中重金属离子的实验研究

分别利用有机柱化剂十二烷基磺酸钠(SDS)和无机柱化剂聚羟基铝(HA)对蛭石进行柱撑制得十二烷基磺酸钠柱撑蛭石(SDS-V erm icu lite)和聚羟基铝柱撑蛭石(HA-V erm icu lite),并通过XRD、红外光谱、ZETA电位等表征手段对柱撑蛭石进行表征,同时针对柱撑蛭石对Cu2 ,Cd2 ,C r3 3种重金属离子的吸附进行研究,结果表明:吸附去除率受反应时间、重金属离子的初始浓度、pH值等因素的影响,经柱撑后的蛭石对重金属离子吸附的吸附性能比蛭石原矿要强。柱撑蛭石吸附3种重金属离子的动力学吸附过程可用E lov icb方程和双常数方程进行较好的拟合。     

不同沉积变质型铁矿石中磁铁矿-赤铁矿的微区拉曼光谱研究

不同成因类型铁矿石中氧化铁矿物的化学成分和晶体结构存在一定程度的差异。光学显微镜和电子探针分析可以有效地识别铁矿石中氧化铁矿物的形貌与成分,激光拉曼光谱可深入探讨其晶体结构以及微观区域(1~100μm)的相变特征。     

矿物组成对离子吸附型稀土矿中稀土元素浸出效率的影响

稀土开采本质上是利用离子交换作用将稀土元素从矿物(黏土矿物、铁(氢)氧化物)表面解吸下来的过程,厘清不同类型矿物对稀土元素浸出的影响,对于提高开采效率至关重要。(NH₄)₂SO₄溶液是稀土元素浸矿时的常用提取剂,SO₄^2-可以通过与稀土元素络合、改变矿物表面电荷性质以及键桥作用等影响稀土元素在矿物表面的吸附/解吸行为,进而影响浸出效率。本研究以高岭石和水铁矿分别作为黏土矿物和铁(氢)氧化物的代表,通过向离子吸附型稀土原矿中添加不同含量(0、5%和10%)的高岭石或水铁矿,结合批量实验、X射线衍射分析(XRD)、电感耦合等离子体发射光谱仪(ICP-OES)及原位红外光谱(in situ ATR-FTIR)等分析表征手段,模拟不同浸取剂体系(NH₄Cl和(NH₄)₂SO₄)下,矿物类型对稀土元素浸取的影响。结果表明,在空白对照组中(未添加高岭石和水铁矿),NH₄Cl浸出稀土...     

新疆萨尔托海高铝铬铁矿中异常矿物群的发现及意义

在萨尔托海高铝型铬铁矿中发现20余种矿物,包括金刚石、单质铬、自然铁和单质硅等自然元素类;碳化物碳硅石;铁镍、铁镍铬合金等金属合金;方铁矿、金红石、赤铁矿、磁铁矿、钛铁矿、石英和铬尖晶石等氧化物类;方铅矿、闪锌矿、针镍矿、赫硫镍矿和毒砂等硫化物类;镁橄榄石、顽火辉石、透辉石、蛇纹石、锆石和长石等硅酸岩类。这些超高压、强还原性和壳源矿物与俄罗斯极地乌拉尔以及西藏罗布莎铬铁矿可以对比,暗示萨尔托海高铝铬铁矿和高铬铬铁矿一样,可能存在深部地幔成矿阶段。深部地幔矿物以及浅部壳源矿物的发现,暗示萨尔托海铬铁矿的形成可能经历了深部地幔预富集和浅部再造富集成矿两个阶段。     

Adsorption of Pentachlorophenol onto Oxide and Clay Minerals： Surface Reaction Model and Environmental Implications

The adsorption of pentachlorophenol （PCP） onto quartz, kaolinite, illite, montmorillonite and iron oxides has been investigated by batch equilibrium techniques. The pH-dependent isotherms are curves with peak values, the position of which is at about pH = 5-6 depending on the mineral species. Based on distribution of both speciation of surface hydroxyls on minerals and PCP in solution a surface reaction model involving surface complexation and surface electrostatic attraction is presented to fit the pH-dependent isotherms, and both reaction constants are calculated. The results show that on quartz and phyllosilicate minerals the predominant adsorption reaction is surface complexation, meanwhile both of surface electrostatic attraction and surface complexation are involved on the iron oxide minerals. The reaction constants of surface electrostatic adsorption are usually one to three orders in magnitude, larger than that of surface complexation. The concentration-dependent isotherms can be well fitted by Langmnir equation with the correlation coefficient R〉0.93 for kaolinite and iron oxides. The maximum adsorption is found in the order： hematite 〉 lepidocrocite 〉 goethite 〉 kaolinite 〉 quartz 〉 montmorillonite ≈ illite, which can be interpreted by consideration of both reaction mechanism and surface hydroxyl density. The significant adsorption of PCP onto mineral surfaces suggests that clay and iron oxide minerals will play an important role as HIOCs are adsorbed in laterite or latertoid soil, which is widespread in South China.     

Geochemical characteristics,cooling history and mineralization significance of Zhangtiantang pluton in South Jiangxi Province,P.R. China

The zircon SHRIMP dating of the Zhangtiantang granite gave an age of 159±7 Ma., which shows that the granite was produced at the early Late Jurassic. The Ar-Ar plateau ages of biotite and K-feldspar from the Zhangtiantang pluton are 153.2±1.1 Ma and 135.8±1.2 Ma, respectively. The Ar-Ar anti-isochrone ages of biotite and K-feldspar are 152.5±1.7Ma and 135.4±2.7Ma, respectively. The ages represent the isotopic closure ages of minerals in the pluton. The Zhangtiantang granites are regarded as peraluminous crust-derived type granites to possess the typical geochemical characteristics of calc-alkaline rocks on continental margin, with enriched Si, K, Al (average value of A/CNK as 1.18), HREE, Rb, U, and Th, heavily depleted V, Cr, Co, Ni, Ti, Nb-Ta, Zr, Sr, P, and Ba, strongly negative Eu and common corundum normative (average value of C as 1.84). The εNd_(t) values of the Zhangtiantang granite are −5.84 to −7.79, and t _2DM values are 1.69 to 1.83 Ga, which indicates partial melting of continental-crust metamorphic sedimentary rocks during the Middle Proterozoic. The cooling history of the Zhangtiantang granitic pluton indicates that the cooling velocity of pluton was faster (about 67°C/Ma) from zircon (158 Ma) to biotite (152 Ma), and was slower (about12°C/Ma) from biotite (152.5 Ma) to K-feldspar (135.8 Ma). It can be deduced that the temporal gap (about 10 Ma) between the granite formmation and W-Sn mineralization in South China may be related to ordinary magma-hydrothermal processes by the variational cooling curve of the pluton. The Zhangtiantang pluton was formed in a compressive setting, with differentiation evolution and mineralization occurring in a relative relaxation setting.