红旗岭3号含矿岩体地质年龄及其岩石学特征

以1号和7号岩体为代表的红旗岭铜镍硫化物矿床,是兴蒙造山带中典型的岩浆熔离型矿床。矿区内共有30多个镁铁-超镁铁质岩体,3号岩体是其中的含矿岩体,多年来因其地质产状与主要含矿岩体不同被认为形成于燕山期。本次工作对采自不同深度岩心样品中的单矿物角闪石进行⁴⁰Ar/³⁹Ar同位素年代学研究,得到（228.2±3.0 ）Ma的坪年龄和（230.1±7.1）Ma的等时线年龄。该年龄和近年发表的红旗岭1号岩体地质年龄基本一致,说明它们均为早印支期岩浆作用的产物。通过对比分析1号和7号主含矿岩体与3号岩体的岩石地球化学特征发现,无论是稀土元素还是微量元素图解均显示了它们具有相同的配分模式,暗示了这些岩体的同源性特点。     

王水溶样-电感耦合等离子体发射光谱法同时测定铁铜铅锌硫化物矿石中8个元素

建立了王水溶样-电感耦合等离子体发射光谱法同时测定铁、铜、铅、锌硫化物矿中Cu、Pb、Zn、As、Ag、Cd、Hg和Mo等8个元素的分析方法。确定了方法的溶矿及测定条件,用国家一级标准物质GBW07162(多金属贫矿石)和GBW07164(多金属矿石)进行精密度实验,除个别元素外,大多数的元素精密度(RSD,n=11)小于5%,准确度(RE)小于10%。通过一系列硫化物矿石标准物质进行方法验证,检测结果基本都在标准值的误差范围内,符合地质矿产开发的要求。方法简单,同时测定元素较多,线性范围宽,检出限低,尤其有利于硫化物矿石中的亲硫元素As、Ag、Hg的分析,实用性强。     

红旗岭镁铁-超镁铁岩侵入体及铜镍硫化物矿床的成岩成矿机制

红旗岭铜镍矿床地处华北地台与吉黑地槽系接触带--辉发河断裂北侧.区内出露30多个镁铁-超镁铁质岩体,其中1、7号超镁铁岩体中赋存铜镍硫化物矿(床)体.含矿岩体分相明显,各类岩石均具堆积结构.铜镍矿体呈似板状、脉状、透镜状及囊状赋存于超镁铁岩体底部橄榄辉岩相中.岩石学和地球化学研究表明,7号岩体形成以流动分异为主,1号岩体为重力分异;原始岩浆属拉斑玄武质,块状矿石系压滤作用产物,后续岩浆的补给和混合补充了成矿物质,硫化物不混溶程度受挥发分制约,矿床属岩浆深部熔离分异成因,成矿时代为印支期.     

金川铜镍矿床中新生代抬升冷却过程：来自裂变径迹的证据

本文基于热年代学理论,利用锆石和磷灰石裂变径迹测年数据及对磷灰石热史的模拟,分析探讨金川铜镍矿床在中新生代的抬升冷却过程,认为金川超基性岩体自中生代以来一直处于持续的冷却抬升阶段,且在中侏罗世和晚白垩世早期经历了两期快速的抬升冷却事件,推断此事件与青藏高原后期活动时间相对应,证明金川岩体受到该事件的远程效应波及,致使该矿床遭受了一定的改造。     

论金川硫化铜镍矿床中贵金属元素的分带机制

在金川硫化铜镍矿床最大的寓矿体内,贵金属元素存在明显分带:Pt、Pd、Au、Ag含量在边部较低,向中心部位逐渐增高;Os、Ir、Ru、Rh含量在中心部位较低,向边部逐渐增高。通过对实际资料的分析,认为这种分带特征是硫化物液相结晶分异作用造成的。     

东天山二叠纪镁铁-超镁铁质成矿岩体造岩矿物特征及其成因意义

东天山造山带与镁铁-超镁铁质岩体有关的铜镍硫化物矿床数量多,分布集中,是我国重要的铜镍成矿带之一。成矿岩体多以小岩体群形式产出,由西向东分布有白鑫滩、黄山和图拉尔根3个岩体群,大型矿床主要赋存在黄山岩体群内。本文对3个岩体群内成矿岩体的主要造岩矿物进行了系统的对比研究。成矿岩体的主要造岩矿物为贵橄榄石、古铜辉石、单斜辉石、斜长石和角闪石以及少量的铬尖晶石和金云母。橄榄石Al温度计计算结果表明,黄山岩体群内成矿岩体的母岩浆结晶温度介于1 143~1 257℃之间,略低于白鑫滩和图拉尔根岩体群(1 283~1 301℃)。单斜辉石压力计算表明成矿岩体的结晶压力相似,介于0.31~0.33 GPa之间。成矿岩体中均富含含水矿物,且单斜辉石结晶早于斜长石,指示成矿岩体的原始岩浆形成于富水环境。成矿岩体的单斜辉石具有较高的Al/Ti值,铬尖晶石和橄榄石具有与岛弧火山岩相似的矿物学特征,结合区域构造演化,认为东天山镁铁-超镁铁质成矿岩体的原始岩浆是被消减板片交代过的地幔部分熔融的产物。矿物学特征对比显示了黄山岩体群内成矿岩体更富斜方辉石和中性斜长石,且具有较低的铬尖晶石Cr~#值和橄榄石Ca含量。结合前人研究成果和相关地球化学数据,认为相对高的混染程度导致了黄山岩体群的母岩浆富SiO_2和Al_2O_3,同时降低了岩浆的结晶温度。     

Magmatic Sulfide Ni-Cu Deposits in China

Deep-seated magmatic liquation-injection deposits form a major type of magmatic sulfide deposit in China. The reserves of nickel and copper in this type of deposit may attain several hundred thousand tons (e.g.Hongqi 7 and Karatunggu) to nearly ten million tons (e.g.Jinchuan). Those deposits can be classified as large or superlarge deposits. The ore grade is relatively high, commonly with w(Ni)＞1 %.The mineralized intrusions are small in size, generally only 0.0n km2 to 0.n km2, with the largest one not exceeding a few km2. Before intruding, the primary magmas have undergone liquation and partial crystallization at depth; as a result, the magmas have partitioned into barren magma, ore-bearing magma, ore-rich magma and ore magma, which then ascended and injected into the present locations once or multiple times, to form ore deposits. The above-mentioned mineralizing process is known as deep-seated magmatic liquation-injection mineralization. The volume of the barren magma is generally much larger than those of the ore-bearing magma, ore-rich magma and ore magma. In the ascending process, most of the barren magma intruded into different locations or outpoured onto the ground surface, forming intrusions or lava flows. The rest barren magma, ore-bearing magma, ore-rich magmaand ore magma may either multiple times inject into the same place in which rocks and ores are formed or separately inject into different spaces to form rocks and ores. Such deep-seated magmatic liquation-injection deposits have a much smaller volume, greater ore potential and higher ore grade than those of in-situ magmatic liquation deposits. Consequently, this mineralizing process leads to the formation of large deposits in small intrusions.     

吉林红旗岭铜镍硫化物矿床的成矿时代讨论

通过对红旗岭铜镍硫化物矿床1号含矿超镁铁质岩体和8号不含矿镁铁-超镁铁质岩体进行单矿物40Ar-39Ar法测年,得到与铜镍硫化物矿床相关的角闪石与黑云母结晶年龄分别为250 Ma和225 Ma,这一结果与前人所报道的K-Ar法年龄有明显的差异.结合与热液矿化相关的斜长伟晶岩锆石SHRIMP法年龄216 Ma,认为镁铁-超镁铁质岩形成于250 Ma左右的印支早期,铜镍硫化物矿床的形成时间晚于含矿岩体,大约为225 Ma前后的印支中期.216 Ma前后的岩浆期后热液叠加对成矿具有积极作用.     

Hydrogen sulfide measurements in air by passive/diffusive samplers and high-frequency analyzer: A critical comparison

In this study, hydrogen sulfide (H₂S) measurements in air carried out using (a) passive/diffusive samplers (Radiello^® traps) and (b) a high-frequency (60 s) real-time analyzer (Thermo^® 450i) were compared in order to evaluate advantages and limitations of the two techniques. Four different sites in urban environments (Florence, Italy) and two volcanic areas characterized by intense degassing of H₂S-rich fluids (Campi Flegrei and Vulcano Island, Italy) were selected for such measurements. The concentrations of H₂S generally varied over 5 orders of magnitude (from 10⁻¹–10³ μg/m³), the H₂S values measured with the Radiello^® traps (H₂S_R) being significantly higher than the average values measured by the Thermo^® 450i during the trap exposure (H₂S_Ta), especially when H₂S was <30 μg/m³. To test the reproducibility of the Radiello^® traps, 8 passive/diffusive samplers were contemporaneously deployed within an 0.2 m² area in an H₂S-contaminated site at Mt. Amiata (Tuscany, Italy), revealing that the precision of the H₂S_R values was ±49%. This large uncertainty, whose cause was not recognizable, is to be added to that related to the environmental conditions (wind speed and direction, humidity, temperature), which are known to strongly affect passive measurements. The Thermo^® 450i analyzer measurements highlighted the occurrence of short-term temporal variations of the H₂S concentrations, with peak values (up to 5732 μg/m³) potentially harmful to the human health. The Radiello^® traps were not able to detect such temporal variability due to their large exposure time. The disagreement between the H₂S_R and H₂S_Ta values poses severe concerns for the selection of an appropriate methodological approach aimed to provide an accurate measurement of this highly toxic air pollutant in compliance with the WHO air quality guidelines. Although passive samplers may offer the opportunity to carry out low-cost preliminary surveys, the use of the high-frequency H₂S analyzer is preferred when an accurate assessment of air quality is required. In fact, the latter provides precise real-time measurements for a reliable estimation of the effective exposure to hazardous H₂S concentrations, giving insights into the mechanisms regulating the dispersion of this air pollutant in relation to the meteorological parameters.