高岭石-伊利石-透辉石体系假相图

采用较纯透辉石岩、高岭石粘土和伊利石粘土作为端元组分,并根据用 DTA、热台显微镜、XRD 方法测定的数据组成了三元体系的假相图。根据假相图说明了有关陶瓷工艺学和变质岩岩石学的一些问题。     

骨灰－伊利石－高岭石体系假相图的研究

采用骨灰、伊利石粘土和高岭石粘土作为端元组分,并根据DTA、热台显微镜、互RD方法测定的数据,组成了这个三元体系的假相图。依据假相图讨论了该体系的热相变特征以及有关骨灰瓷工艺学问题。     

骨灰－伊利石－高岭石体系假相图的研究

采用骨灰、伊利石粘土和高岭石粘土作为端元组分，并根据ＤＴＡ、热台显微镜、互ＲＤ方法测定的数据，组成了这个三元体系的假相图。依据假相图讨论了该体系的热相变特征以及有关骨灰瓷工艺学问题。     

硅灰石的单独测定

硅灰石作为工业矿物应用于陶瓷、涂料,塑料及橡胶工业等方面。硅灰石矿物夹杂有方解石、白云石和透辉石;地质工作者欲求得硅灰石矿物组分含量,一般由大量岩石全分析数据来计算;此法不     

硅灰石的单独测定

硅灰石作为工业矿物应用于陶瓷、涂料、塑料及橡胶工业等方面。硅灰石矿物夹杂有方解石、白云石和透辉石;地质工作者欲求得硅灰石矿物组分含量,一般由大量岩石全分析数据来计算;此法不     

大义山硅灰石矿石矿物含量计算方法

大义山硅灰石矿床矿石矿物组合复杂,由硅灰石、透辉石、符山石、钾长石、钠长石、方解石、石英等组成。矿床评价需要测定矿石中的硅灰石的含量。岩矿鉴定用薄片测定的结果缺乏代表性。本文介绍了用矿石化学成分分析数据换算成硅灰石含量的具体步骤。     

硅灰石浮选新工艺问世

富含石榴石透辉石的矽卡岩型硅灰石．国内外公认属难选矿石，一般是采用强磁选-浮选-强磁选的联合流程。近期，经武汉工业大学方和平副教授等数年研制，推出单一浮选新工艺及新的药剂制度连续浮选，有效地实现了硅灰石与方解石、透辉石、石榴石、石英的分离，     

关于硅灰石化学分析项目的研究

硅灰石矿物是一种自然产出的偏硅酸钙,其分子式为[CaO·SiO_2]_3,理论组成是CaO48.3％、SiO_251.7％。它作为工业矿物仅有卅年的历史,由于它具有低温快速烧成的窑业性能,近几年来已引起国内外有关行业的重视。其化学分析项目仍沿用了最初规定的SiO_2、CaO、MgO、Fe_2O_3、Al_2O_3和灼减等6项。从吉林省所发现的几处硅灰石产地来看,其主要矿物成份是硅灰石、方解石、尚有少量白云石、透辉石、石榴石和葡萄石伴生。测定SiO_2、CaO是想知道矿物的主要成份;测定MgO想知道矿物中透辉石、白云石的含量;测定Al_2O_3想知道矿物中石榴石的含量;测定Fe_2O_3想了解矿物中的有害成份;测定灼减想知道矿物中CO_2的大概数。一般说来测定这6个项目基本上能判定硅灰石的质量。对硅灰石矿床进行工业评价时,主要以矿石中有益矿物硅灰石和     

广西平乐硅灰石矿工艺矿物学研究

对广西平乐硅灰石矿的化学成分和矿物组成进行了分析确定，对硅灰石及其伴生矿物的结构构造特征进行了查定，主要对硅灰石中碳质物的赋存特征进行了研究，发现硅灰石矿石中的碳质物分别与硅灰石、方解石、石英等多种矿物以多种形式紧密伴生，认为要提高平乐硅灰石粉的白度，除了要尽可能除去透辉石、石榴石等矿物杂质及含铁、锰等的氧化物杂质外，关键还要使碳质物单体解离，并除去碳质物杂质。     

西藏甲玛3000 m科学深钻矽卡岩矿物分带及地质意义

甲玛铜多金属矿床是冈底斯成矿带东段具有重大经济价值及科学研究意义的超大型斑岩- 矽卡岩矿床,完整地保存了矽卡岩矿床形成和演化的重要信息。前人研究多集中于矽卡岩的水平分带,而对于矽卡岩矿物垂直分带以及其与金属矿化的耦合关系等方面研究薄弱。本文重点对甲玛3000 m科学深钻中矽卡岩矿体进行了精细的矿物学研究,系统揭示了矽卡岩矿体的矿物学空间分带特征以及与金属矿化的耦合关系。结果表明,矽卡岩从浅部至深部具有清晰的分带现象,即矽卡岩化角岩→透辉石石榴子石矽卡岩→硅灰石石榴子石矽卡岩→石榴子石硅灰石矽卡岩→透辉石石榴子石矽卡岩→石榴子石硅灰石矽卡岩→矽卡岩化大理岩→硅灰石石榴子石矽卡岩→透辉石石榴子石矽卡岩→硅灰石石榴子石矽卡岩→矽卡岩化大理岩→硅灰石石榴子石矽卡岩→透辉石石榴子石矽卡岩→内矽卡岩（含石榴子石花岗闪长斑岩）。金属矿物组合从浅部向深部,变化为辉钼矿±黄铜矿→斑铜矿+黄铜矿±辉铜矿±硫铋铜矿±辉钼矿→辉钼矿±黄铜矿,对应成矿元素变化为Mo±Cu±Au±Ag→Cu（Mo）±Au±Ag→Mo±Cu±Au±Ag。研究表明,侵入岩及围岩的空间位置、构造环境、多期次热液流体叠加是控制矽卡岩矿物分带的重要因素。同时,矿物学特征表明,矽卡岩中高品位金的富集与斑铜矿等铜硫化物密切相关,也可能与多期次流体叠加和富金岩浆源区有关。     

相图在透闪石和透辉石锦砖配方设计中的应用

文章指出了陶瓷生产中应用相图的要点和设计配方时应注意的问题,并着重从CaO-MgO-Al2O3-SiO2四元系统相图和K2O-Al2O3-SiO2三元系统相图讨论了透闪石和透辉石用于陶瓷锦砖生产中之新体系配方设计的思路。认为纯粹用这两种原料为助熔剂生产锦砖节能效益不十分明显。在传统的锦砖配方中加入适当的透闪石或透辉石可明显地降低产品的烧成温度,但会使坯体的烧成范围变窄。文章强调具有实际意义的配方是具有相当宽烧成范围的低温配方。     

Humite- and scapolite-bearing assemblages in marbles and calcsilicates of Dronning Maud Land, Antarctica: new data for Gondwana reconstructions

This study investigates marbles and calcsilicates in Central Dronning Maud Land (CDML), East Antarctica. The paleogeographic positioning of CDML as part of Gondwana is still unclear; however, rock types, mineral assemblages, textures and P–T conditions observed in this study are remarkably similar to the Kerala Khondalite Belt in India. The CDML marbles and calcsilicates experienced a Pan-African granulite facies metamorphism at c. 570 Ma and an amphibolite facies retrogression at c. 520 Ma. The highest grade assemblage in marbles is forsterite+spinel+calcite+dolomite, in calcsilicates the assemblages are diopside+spinel, diopside+garnet, scapolite+wollastonite+clinopyroxene±quartz, scapolite±anorthite±calcite+clinopyroxene+wollastonite. These assemblages constrain the peak metamorphic conditions to 830±20 °C, 6.8±0.5 kbar and X _CO2>0.46. During retrogression, highly fluoric humite-group minerals (humite, clinohumite, chondrodite) replaced forsterite, and garnet rims formed at the expense of scapolite during reactions with wollastonite, calcite or clinopyroxene but without involvement of anorthite. Metamorphic conditions were about 650 °C, 4.5±0.7 kbar, 0.2< X _CO2^fluid<0.36, and the co-existence of garnet, clinopyroxene, wollastonite and quartz constrains f_O2 to FMQ-1.5 log units. Mineral textures indicate a very limited influx of H₂O-rich fluid during amphibolite facies retrogression and point to significant variations of fluid composition in mm-sized areas of the rock. Gypsum was observed in two samples; it probably replaced metamorphic anhydrite which appears to have formed under amphibolite facies conditions. The observed extensive anorogenic magmatism (anorthosites, A-type granitoids) and the character of metamorphism between 610 and 510 Ma suggest that the crustal thermal structure was characterized by a long-lived (50–100 Ma) rise of the crustal geotherm probably caused by magmatic underplating.     

Calc-silicate reactions and bedding-controlled isotopic exchange in the Notch Peak aureole, Utah: implications for differential fluid fluxes with metamorphic grade

Fluid compositions and bedding‐scale patterns of fluid flow during contact metamorphism of the Weeks Formation in the Notch Peak aureole, Utah, were determined from mineralogy and stable isotope compositions. The Weeks Formation contains calc‐silicate and nearly pure carbonate layers that are interbedded on centimetre to decimetre scales. The prograde metamorphic sequence is characterized by the appearance of phlogopite, diopside, and wollastonite. By accounting for the solution properties of Fe, it is shown that the tremolite stability field was very narrow and perhaps absent in the prograde sequence. Unshifted oxygen and carbon isotopic ratios in calcite and silicate minerals at all grades, except above the wollastonite isograd, show that there was little to no infiltration of disequilibrium fluids. The fluid composition is poorly constrained, but X(CO₂)_fluid must have been >0.1, as indicated by the absence of talc, and has probably increased with progress of decarbonation reactions. The occurrence of scapolite and oxidation of graphite in calc‐silicate beds of the upper diopside zone provide the first evidence for limited infiltration of external aqueous fluids. Significantly larger amounts of aqueous fluid infiltrated the wollastonite zone. The aqueous fluids are recorded by the presence of vesuvianite, large decreases in δ¹⁸O values of silicate minerals from c. 16‰ in the diopside zone to c. 10‰ in the wollastonite zone, and extensive oxidation of graphite. The carbonate beds interacted with the fluids only along margins where graphite was destroyed, calcite coarsened, and isotopic ratios shifted. The wollastonite isograd represents a boundary between a high aqueous fluid‐flux region on its higher‐grade side and a low fluid‐flux region on its lower‐grade side. Preferential flow of aqueous fluids within the wollastonite zone was promoted by permeability created by the wollastonite‐forming reaction and the natural tendency of fluids to flow upward and down‐temperature near the intrusion‐wall rock contact.     

硅灰石矿化学物相分析方法

硅灰石是一种钙的偏硅酸盐矿物,它作为工业矿物仅有二十多年的历史。从六十年代起,硅灰石用作陶瓷原料有了迅速地发展,由于能低温快速烧成,可大幅度降低燃料消耗,缩短生产周期,提高生产率。因此,大量用于釉面砖的生产。此外,硅灰石还在涂料工业、塑料与橡胶工业、磨料工业、电焊和绝缘产品等方面也得到应用,特别是把硅灰石处理成超细粒材料后,更有广阔的发展前景。     

The surface chemistry of multi-oxide silicates

The surface chemistry of natural wollastonite, diopside, enstatite, forsterite, and albite in aqueous solutions was characterized using both electrokinetic techniques and surface titrations performed for 20 min in batch reactors. Titrations performed in such reactors allow determination of both proton consumption and metal release from the mineral surface as a function of pH. The compositions, based on aqueous solution analysis, of all investigated surfaces vary dramatically with solution pH. Ca and Mg are preferentially released from the surfaces of all investigated divalent metal silicates at pH less than ∼8.5-10 but preferentially retained relative to silica at higher pH. As such, the surfaces of these minerals are Si-rich and divalent metal poor except in strongly alkaline solutions. The preferential removal of divalent cations from these surfaces is coupled to proton consumption. The number of protons consumed by the preferential removal of each divalent cation is pH independent but depends on the identity of the mineral; ∼1.5 protons are consumed by the preferential removal of each Ca atom from wollastonite, ∼3 protons are consumed by the preferential removal of each Mg or Ca atom from diopside or enstatite, and ∼4 protons are consumed by the preferential removal of each Mg from forsterite. These observations are interpreted to stem from the creation of additional ‘internal’ adsorption sites by the preferential removal of divalent metal cations which can be coupled to the condensation of partially detached Si. Similarly, Na and Al are preferentially removed from the albite surface at 2 > pH > 11; mass balance calculations suggest that three protons are consumed by the preferential removal of each Al atom from this surface over this entire pH range. Electrokinetic measurements on fresh mineral powders yield an isoelectric point (pH_IEP) 2.6, 4.4, 3.0, 4.5, and <1, for wollastonite, diopside, enstatite, forsterite, and albite, respectively, consistent with the predominance of SiO₂ in the surface layer of all of these multi-oxide silicates at acidic pH. Taken together, these observations suggest fundamental differences between the surface chemistry of simple versus multi-oxide minerals including (1) a dependency of the number and identity of multi-oxide silicate surface sites on the aqueous solution composition, and (2) the dominant role of metal-proton exchange reactions on the reactivity of multi-oxide mineral surfaces including their dissolution rate variation with aqueous solution composition.     

Steady-diffusion modelling of a reaction zone between a metamorphosed basic dyke and a marble from Hirao-dai, Fukuoka, Japan

A reaction zone between a metamorphosed basic dyke and marble at Hirao-dai, north Kyushu, Japan, consists of well-organized sequential zones of diopside, garnet and wollastonite; textures are characteristic of diffusion-controlled structures. The reaction zone formed during contact metamorphism associated with intrusion of a Cretaceous granodiorite at ∼300 MPa and 700 °C. The metamorphosed basic dyke consists of diopside, biotite and plagioclase ( X _Ab = 0.4–0.8), whereas the marble is almost pure calcite. The initial boundary between the dyke and the marble is probably located within the current diopside zone, as calcite occurs as remnants among diopside grains in areas close to the boundary with the garnet zone. This observation provides a criterion to judge the stability of the zonal sequence in our modelling. The formation of the reaction zone is attributed to a single-stage steady-state process with five overstepping reactions. CaO, MgO, FeO, SiO₂ and AlO_3/2 are the reaction-controlling components that are necessary to describe the growth of the reaction zone. An isochemical steady-diffusion model cannot reproduce the measured phase ratios of product minerals; this indicates open-system behaviour of the reaction zone. The choice of closure components is an essential task in the treatment of open-system modelling, together with determination of phase ratios (Ashworth & Birdi model) or estimation of boundary fluxes (Johnson & Carlson model). Of all the possible combinations of closure components, closure conditions for CaO and MgO provide the best results for both models. The stability of the zonal sequence is limited at relatively large values of L _SiSi/ L _CaCa. Similar results from the two models confirm their consistency under the same closure conditions.     

Thermochemistry of carbonate-pyroxene equilibria

The enthalpies of drop solution of calcite, magnesite, dolomite, wollastonite and diopside have been measured in a lead borate solvent at 977 K in a Calvettype microcalorimeter. The carbonate calorimetry was done under flowing gas atmosphere. Both natural and synthetic samples were used. From these calorimetric data, the enthalpies of several reactions of carbonate with quartz were calculated. The enthalpies of these reactions (kJ/mol) at 298 K are: calcite+quartzwollastonite+CO₂, 92.3±1.0; magnesite+quartzenstatite+CO₂, 82.9±2.8; dolomite+quartzdiopside+CO₂, 163.0±1.9. These values generally are in agreement with those calculated from Robie et al., Helgeson et al., Berman and Holland and Powell. The enthalpy of dolomite-quartz reaction overlaps marginally with those from Berman and Holland and Powell. The enthalpy of formation of dolomite from magnesite and calcite (-11.1±2.5 kJ/mol) was also derived from the measured enthalpies, and this value is consistent with that from acid solution calorimetric measurements as shown by Navrotsky and Capobianco, but different from values in the earlier literature. These results support the premise that drop-solution of carbonates into molten lead borate results in a well-defined final state consisting of dissolved oxide and evolved CO₂. This was also confirmed by weight change experiments. Thus, oxide melt calorimetry is applicable to carbonates.     

Stable Isotope Evidence for the Role of Diffusion, Infiltration, and Local Structure on Contact Metamorphism of Calc-Silicate Rocks at Noth Peak, Utah

The effects of infiltration, diffusion, and local structureon the contact metamorphism of the Cambrian Weeks Formation,a calcareous argillite located in western Utah, were examinedusing stable isotope systematics and mineral mass-balance considerations.The emplacement of the Jurassic Notch Peak granitic stock resultedin metamorphism characterized with increasing proximity to theintrusion by phlogopite, diopside, and wollastonite isograds.The isograds are generally concentric around the stock, withdiopside and wollastonite isograds {small tilde}600 and 400m from the contact, respectively, but are deflected near a pre-intrusionfault where the wollastonite isograd is 1. 5 km from the contact.Where the isograds are concentric, the wollastonite isogradmarks an isotopic front with whole-rock ¹⁸O values approachingthe 9.5% value of the stock. In contrast, the ¹⁸O values inthe unmetamorphosed to diopside-grade rocks range from 16.3to 20.2%. Near the fault the isotopic front extends throughthe diopside zone, suggesting that the fault was a major conduitfor magmatic water. Water—rock ratios for the diopside- and wollastonite-gradesamples determined from mineralogic mass balance are nearlyone order of magnitude larger than ‘one-box’ closed-systemratios determined from shifts in stable isotope ratios. Chromatographicmodels for isotopic exchange and propagation of isograds showthat one-dimensional infiltration of magmatic water throughpore spaces would lead to an isotopic front at 50 m from thestock and the wollastonite isograd would be only 8 km from thestock. These distances are significantly smaller than observed.It is suggested that most of the magmatic water flowed throughfractures or thin permeable layers, with the extent of isotopicexchange between the magmatic water in these conduits and theadjacent rocks being controlled by the extent of reaction progressin the rocks. Considerations of CO₂—H₂O interdiffusivitiesin fluids indicate that removal of CO₂ from the reaction frontstoward the intrusion or the fault was sufficiently rapid tocontrol the geometry of the isograds.