Genesis of the Kamioka Skarn Deposits: An Important Role of Clinopyroxene Skarn and Graphite-bearing Limestone in Precipitating Sulfide Ore

Abstract: A genetical relationship between skarn formation and mineralization is investigated for the Kamioka skarn deposits which are the largest Zn-Pb producer in Japan. In the Mozumi deposit, one of main deposits in the Kamioka mining area as well as Tochibora and Maruyama, clinopyroxene skarn was generally subjected to later replacement by garnet or magnetite–calcite–quartz during the Zn-Pb mineralization. The replacement of hedenbergitic clinopyroxene by andraditic garnet resulted in the formation of diopsidic clinopyroxene relicts. With the progress of replacement, the S/So value (So: an estimated area occupied by an original clinopyroxene grain in a thin section, S: a total area of relict clinopyroxene fragments) which is an index of the degree of replacement decreases from 0. 7 to 0. 1, and the hedenbergite mole percent of relict clinopyroxene decreases drastically from about 65 to less than 40. A close association of andraditic garnet and sphalerite suggests that heden-bergitic clinopyroxene skarn played an important role to reduce the relatively oxic ore-forming fluid enriched in Zn²⁺ and SO4^2– and to precipitate sphalerite from the fluid. Ferrous iron in the hedenbergitic clinopyroxene skarn was oxidized to form andraditic garnet. Besides this garnet formation, the mineral assemblage of magnetite–calcite–quartz replaced the clinopyroxene skarn at the time of mineralization. In both cases, the reduction of relatively oxic ore-forming fluid by hedenbergitic clinopy-roxene skarn at the later stage brought about the precipitation of sulfide minerals. In contrast, these types of later replacement are not found in the Tochibora deposit. Instead, graphite-bearing crystalline limestone and relatively fresh clinopyroxene skarn are common. Mineralized clinopyroxene skarn has high graphite carbon contents relative to barren one, suggesting that the amount of graphite in the skarn was an important controlling factor for mineralization. It is very likely that the graphite played a role of reducing agent during the mineralization in the Tochibora deposit.     

Experimental research on a new encapsulated heat-generating hydraulic fracturing fluid system

1 IntroductionFracturing plays an important role in increasingthe production and injection and enhancing the final re-covery of oil and gas. At present, the use of ahydroxypropyl guar gum, borate-crosslinked, hydraulicfracturing fluid systemhas become ext…     

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。     

Effect of structure-directing agent on AlPO4-n synthesis from aluminum dross

The hydrothermal synthesis of AlPO₄-n which is a functional material of aluminophosphate, was conducted from two kinds of aluminum dross discharged in an aluminum regeneration factory. The effect of structure-directing agent (SDA) on the formation behavior of AlPO₄-n from aluminum dross, the suitable condition to obtain AlPO₄-n efficiently, and the pore structure and gas adsorption property were investigated in this study.AlPO₄-5 and AlPO₄-34 are mainly formed from aluminum dross as a raw material, and it is possible to make AlPO₄-5 successfully as a main product by adjusting the amount of triethylamine (TEA) as SDA. The gas adsorption amount with AlPO₄-5 is the following order; ammonia > dipropylamine > benzene, and it is found that this order mainly corresponds with the polarity of molecule among them.     

添加剂对KAlSi_3O_8-CaSO_4-CaCO_3体系反应表观活化能的影响

首先测定了KAlSi3O8-CaSO4-CaCO3体系在不同焙烧条件下钾长石转化成可溶性氧化钾的转化率,进而通过模拟计算表明:KAlSi3O8-CaSO4-CaCO3体系的固相扩散动力学过程符合金斯特林格动力学方程,反应表观活化能Ea为128.92kJ/mol。并着重考察了4种添加剂Na2SO4、Na2SO3、NaCl和NaF对KAlSi3O8-CaSO4-CaCO3体系的影响,结果表明:向体系中分别加入占反应物总质量3%的Na2SO4、Na2SO3、NaCl和1%的NaF后,体系的反应表观活化能Ea从原来的128.92kJ/mol依次下降至87.15、98.71、117.38和126.14kJ/mol,这表明4种添加剂中Na2SO4的效果最好,它能较大程度上降低反应表观活化能,从而降低反应温度和提高固相反应速率。     

泥浆凝集剂凝集机理分析与选择

对泥浆凝聚与絮凝机理作了探讨，指出了常用的凝集剂，并通过比较指出了其选择方法。     

Sensitive Ion‐Flotation Separation of Ag(I) Traces Using 2‐(2‐Methoxyphenyl)benzimidazole before Flame Atomic Absorption Spectrometric Determination in Water

A sensitive, reliable, and environmentally friendly method for simple separation and preconcentration of Ag(I) traces in aqueous samples is presented prior to their flame atomic absorption spectrometric determinations. At pH 7.0, Ag(I) was separated with 2‐(2‐methoxyphenyl)benzimidazole (MPBI) as a new complexing agent and floated after adding sodium dodecyl sulfate (SDS) as a foaming reagent. The floated layer was then dissolved in proper amount of concentrated nitric acid in methanol and introduced to the flame atomic absorption spectrometer (FAAS). The effects of pH, concentration of MPBI, type and amount of surfactant as the floating agent, type and amount of eluting agent, and influence of foreign ions on the recovery of the analyte ion were investigated. Also, using a nonlinear curve fitting method, the formation constant of 1.62 × 10⁶ was obtained for Ag(I)–MPBI complex. The analytical curve was linear in the range of 1.8 × 10^?7–1.7 × 10^?6 mol/L for determination of Ag(I). The relative standard deviation (RSD; N = 10) corresponding to 0.7 × 10^?6 mol/L of Ag(I), the limit of detection (10 blanks), and the enrichment factor were obtained as 1.7%, 2.9 × 10^?8 mol/L, and 43.0, respectively. The proposed procedure was then applied successfully for determination of silver ions in different water samples.     

地下爆炸成腔注浆支护的小型实验研究

针对爆扩成腔稳定性差、渗水率高及遇水坍塌等问题，采用注浆抽浆法对爆炸空腔进行了支护，并进行防渗小型实验研究。确定了注浆临界水灰比为0.8:1，分别对重力注浆、压力注浆以及压力注浆加防水剂和无支护的4个空腔进行了支护对比实验。实验表明：重力注浆不足以达到要求，压力注浆是一种解决支护和防渗较为可行的方法，加入防水剂后效果更好。     

铝土矿矿泥固化技术的试验研究

铝土矿选洗过程中排尾形成的高含水量矿泥,传统上采用建库堆存,泌干固结时间长,污染环境。试验研究结果表明,选用由72%水泥、20%石膏、5%石灰、3%硫酸钠组成的复合固化剂,或由72%石灰、20%石膏、5%粉煤灰、3%硫酸钠组成的复合固化剂,按固化剂与矿泥质量比1:10掺加,对矿泥进行固化处理,其固化体强度高、耐久性好,且成本低廉,具有广泛的工程应用价值。     

剥片高岭土的有机改性

用醋酸钾进行插层形成高岭土—醋酸钾复合体。通过X射线检测，高岭土层间距明显增大。将此复合体通过水洗，除去醋酸钾，高岭土即被剥片。剥片后高岭土粒径变小，但保持了高岭土的基本层状结构。用偶联剂对剥片后高岭土进行有机改性，形成高岭土有机复合物。“有效活化指数”的测定实验表明，利用此种方法制备的剥片高岭土有机改性效果很好。