Silicate‐oxide mineral chemistry of mafic–ultramafic rocks as an indicator of the roots of an island arc: The Chilas Complex,Kohistan (Pakistan)

The Chilas Complex is a major lower crustal component of the Cretaceous Kohistan island arc and one of the largest exposed slices of arc magma chamber in the world. Covering more than 8000 km², it reaches a current tectonic width of around 40 km. It was emplaced at 85 Ma during rifting of the arc soon after the collision of the arc with the Karakoram plate. Over 85% of the Complex comprises homogeneous, olivine‐free gabbronorite and subordinate orthopyroxene–quartz diorite association (MGNA), which contains bodies of up to 30 km² of ultramafic–mafic–anorthositic association (UMAA) rocks. Primary cumulate textures, igneous layering, and sedimentary structures are well preserved in layered parts of the UMAA in spite of pervasive granulite facies metamorphism. Mineral analyses show that the UMAA is characterized by more magnesian and more aluminous pyroxene and more calcic plagioclase than those in the MGNA. High modal abundances of orthopyroxene, magnetite and ilmenite (in MGNA), general Mg–Fe–Al spatial variations, and an MFA plot of whole‐rock analyses suggest a calc‐alkaline origin for the Complex. Projection of the pyroxene compositions on the Wo–En–Fs face is akin to those of pyroxenes from island arcs gabbros. The presence of highly calcic plagioclase and hornblende in UMAA is indicative of hydrous parental arc magma. The complex may be a product of two‐stage partial melting of a rising mantle diaper. The MGNA rocks represent the earlier phase melting, whereas the UMAA magma resulted from the melting of the same source depleted by the extraction of the earlier melt phase. Some of the massive peridotites in the UMAA may either be cumulates or represent metasomatized and remobilized upper mantle. The Chilas Complex shows similarities with many other (supra)subduction‐related mafic–ultramafic complexes worldwide.     

水玻璃固化硫酸盐渍土强度特性及固化机制研究

盐渍土化学固化法是解决盐渍土盐胀、溶陷和腐蚀等不良工程问题的有效方法之一。通过无侧限抗压强度试验、X射线衍射试验、化学成分分析和扫描电镜试验研究了石灰粉、煤灰、水玻璃联合固化硫酸盐渍土的强度特征,分析探讨了其固化机制。试验结果表明：石灰含量小于8%时,石灰、粉煤灰、水玻璃联合固化硫酸盐渍土的抗压和抗剪强度较石灰粉煤灰固化土有大幅度提升,固化土强度随水玻璃浓度几乎呈线性增长。水玻璃固化硫酸盐渍土强度增加的机制在于：水玻璃的碱激发粉煤灰作用和水玻璃与盐渍土中化学成分的吸附作用所生成各类凝胶的填充和包裹,使得骨架颗粒的接触面积增大,颗粒之间的孔隙逐步减小,骨架颗粒由点接触变为面接触,固化盐渍土通过凝胶而黏结成为一个紧密的空间网状整体结构,土体强度得以提高。同时,复杂的物理化学作用大幅度降低了固化盐渍土中 含量,有效地抑制了硫酸盐渍土的盐胀特性。     

Determination of Ge, As, Se and Te in Silicate Samples Using Isotope Dilution-Internal Standardisation Octopole Reaction Cell ICP-QMS by Normal Sample Nebulisation

A method for the determination of Ge, As, Se and Te in silicate samples using isotope dilution-internal standardisation (ID-IS) octopole reaction cell (ORC) ICP-QMS by normal sample nebulisation was developed. The method does not involve either hydride generation or ion exchange. Germanium, Se and Te were determined by isotope dilution (ID), and As was determined by ID-IS. A silicate sample with an added Ge-Se-Te spike was digested with an HF-HNO₃-HBr mixture, dried, re-dissolved with HF and the supernatant liquid was directly aspirated into an ORC-ICP-QMS instrument with He or H₂ gas. No matrix effects were observed down to a dilution factor (DF) of ∼ 70 for Ge, Se and Te and DF of ∼ 1000 for As, which resulted in 3s detection limits in silicates of 2, 1, 0.1 and 4 ng g⁻¹, respectively. Advantages of the method are the simple sample introduction as well as a capability of determining S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by ID-IS-ICP-QMS/SFMS from the same solution. Furthermore, the total sample solution consumption was only 0.253 ml with DF = 2000. Therefore, only a 0.13 mg test portion was required. To demonstrate the applicability of this technique, Ge, As, Se and Te in eight silicate reference materials were determined, as well as S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta in four carbonaceous chondrites.     

硅酸盐聚乙稀醇冲洗液在新疆砂岩性铀矿钻探中的应用

分析并研究了硅酸盐聚合物冲洗液体系的作用机理,配制了一套专门针对砂岩性铀矿岩心钻探中复杂地层孔段长、极易引发多种孔内事故的冲洗液体系。生产实践证明,该冲洗液体系完全能够满足绳索取心钻进工艺各项性能要求,并在对付砂岩性复杂地层方面具有良好的效果。     

金在花岗质熔体中溶解度的初步实验研究

以合成花岗岩、水、不同浓度的盐酸溶液、氢氟酸溶液作为反应初始物,在850℃,100 MPa,接近于NNO的条件下开展了金在不同花岗质熔体中溶解度的实验研究,实验固液相产物中的金含量使用石墨炉原子吸收法测定。实验结果显示,金在花岗质熔体中的溶解度变化范围为1.87～156.62μg/g,流体相中金的溶解度为0.31～6.92μg/g;金在熔体相中的溶解度较其在共存液相中的高。花岗质熔体相中金的溶解度明显受熔体化学组成的影响,过碱性富钠花岗质熔体中金的溶解度明显高些;金在花岗质熔体中的溶解度随着熔体中Na2O/K2O摩尔比增大而增大;在氟氯共存岩浆体系中,氟含量变化对金在熔体相中的溶解度影响不明显,而液相中氯含量增大有利于提高金在流体相中的含量。     

胶质芽孢杆菌－蒙脱石相互作用实验研究

利用硅酸盐细菌研究了微生物对硅酸盐矿物的分解作用。选取层状硅酸盐矿物蒙脱石在30℃与一株编号为3025的硅酸盐细菌B.mucilaginosus进行交互作用,并利用电感耦合等离子体发射光谱仪(ICP-AES)分析溶液中Si、Al、Mg离子的出溶量,利用X射线衍射(XRD)和显微红外光谱(Micro-FTIR)分析微生物作用后矿物物相和微结构变化。发现经硅酸盐细菌作用后,蒙脱石化学成分及晶体结构发生了细微变化,为微生物活动促进粘土矿物分解作用研究提供了实验和理论依据。     

珠江三角洲滨海小流域离子化学特征及来源分析

在分析中山大学滨海小流域水循环综合试验基地内雨水、河水和地下水离子组分的基础上,讨论了该小流域内水体离子化学组分的特征及来源。结果显示:①河水中TDS变化范围为28.97～44.64 mg/l,平均值为33.90 mg/l;在离子化学组成中,阳离子以Na++K+为主,阴离子以Cl-和HCO3-为主;雨水中TDS的变化范围为0.88～26.07 mg/l,平均值为8.42 mg/l,离子含量变化幅度较大;地下水TDS变化范围为39.49～113.16 mg/l,均值为58.11 mg/l,约为流域河水的2倍,雨水的7倍;②海盐沉降中Ca2+、Mg2+、Na+、K+、SO42-的贡献率:雨季分别为6%、60%、47%、2%和15%,旱季分别为3%、41%、54%、2%、9%;③硅酸盐风化中,雨季:(Ca/Na)sil=0.31,(Mg/K)sil=0.21;旱季:(Ca/Na)sil=0.36,(Mg/K)sil=0.27;CO2消耗率为12.4 t/(km2.a);④河水中的NO3-和(SO42-)res主要来源于大气酸沉降,且具有旱季含量低、雨季含量高的特点;⑤R1潜水井受到一定程度的NO3-污染,NO3-的...     

X射线荧光光谱法测定高锶高钡的硅酸盐样品中主量元素

用百分总和检查硅酸盐岩石全分析数据的质量是分析工作者的传统做法,但对于微量元素含量较高的样品,采用X射线荧光光谱法(XRF)进行测定,如果不考虑微量元素的含量及其对主量元素基体效应的影响,往往会使主量元素含量更加偏离真实值。本文针对Sr、Ba含量较高的硅酸盐样品,通过人工配制标准样品,扩大了Sr、Ba校准曲线的定量范围,主量元素校准中加入Sr、Ba的基体校正系数,达到了主量元素定量更加准确可靠的实际效果。采用此方法分析国家标准物质,各主量元素的精密度(RSD)均小于2%;分析不参加回归的标准物质和人工配制的标准样品,主量元素的测量值与标准值(或参考值)基本一致。该方法可以满足硅酸盐的测定要求,主量元素各项结果的加和能够达到《地质矿产实验室测试质量管理规范》的一级标准(99.3%～100.7%)。     

An Optimised 1,10‐Phenanthroline Method for the Determination of Ferrous and Ferric Oxides in Silicate Rocks,Soils and Minerals

A precise, accurate and rapid method for the sequential determination of FeO and Fe₂O₃ in rocks, soils and some non‐refractory minerals by 1,10‐phenanthroline spectrophotometry is described. Fe(II) and Fe(III) were leached from the sample (?200 mesh) using a mixture of NH₄HF₂ and H₂SO₄ at 40–80 °C for 10 min on a hot plate. Both Fe(II) and Fe(III) could be conveniently estimated sequentially from the same reaction mixture at the μg g^?1 to percentage level. The method is better than the existing wet chemical methods, including the commonly used Pratt's titrimetric redox method, for Fe(II) and Fe(III) determinations in rock and soil samples in terms of precision, accuracy and rapidity. The throughput of the method was very high; at least forty to fifty samples could be estimated easily in a day. The results obtained compare favourably with those obtained by Pratt's method, as well as for certified/recommended values of a set of eleven certified reference materials having FeO and Fe₂O₃ contents in the range 0.21–14.63% and 0.58–8.48%, respectively. The optimised 1,10 phenanthroline method was found to be accurate to within 0.21% m/m FeO and 0.30% m/m Fe₂O₃ compared with the literature values of the certified reference materials studied.     

Effect of Mineral Dusts on the Growth of Silicate Bacteria S35

In order to compare the chemical compositions and physical properities of dusts on silicate bacteria S35, the chemical compositions of six kinds of mineral dusts have been analyzed and the changes of pH value, glucose （GLU）, electrolyte and Mn, Si, Fe before and after the dusts reacted with silicate bacteria S35 have been measured. The SEM analysis has been used to study the bacterial form and interface action status in the course of reaction between dusts and bacteria. The results show that these mineral dusts have different effects on experiment bacteria. Therefore, it is concluded that the effect of mineral dusts on silicate bacteria has correlation with the chemical compositions and physical properities of dusts.