西藏多龙矿集区波龙、多不杂斑岩铜金矿床岩体锆石Ce4+/Ce3+比值及氧逸度特征

波龙、多不杂斑岩铜金矿床是青藏高原中部发现的两个大型斑岩铜金矿床。对波龙、多不杂斑岩铜金矿床含矿花岗闪长斑岩和不含矿花岗闪长斑岩的锆石Ce~(4+)/Ce~(3+)比值以及氧逸度等特征进行研究,并且通过计算得到了3个含矿花岗闪长斑岩的锆石Ce~(4+)/Ce~(3+)比值分别为536.03,492.18,454.02;1个不含矿的花岗闪长斑岩的锆石Ce~(4+)/Ce~(3+)比值为0.67。说明波龙、多不杂斑岩矿床中与成矿相关的岩体具有相对更高的氧化状态。对比西藏冈底斯成矿带中的斑岩矿床、云南中甸岛弧成矿带中的烂泥塘斑岩铜矿床、金沙江-红河成矿带中的马厂箐、铜厂铜钼矿以及玉龙成矿带铜钼矿床岩体的锆石Ce~(4+)/Ce~(3+)比值,发现含矿岩体锆石Ce~(4+)/Ce~(3+)比值一般250。结合波龙、多不杂矿床的锆石Ce~(4+)/Ce~(3+)的计算结果发现Ce~(4+)/Ce~(3+)基本300,因此将锆石Ce~(4+)/Ce~(3+)300作为波龙、多不杂矿床斑岩成矿的一个地球化学标志。此外,通过(Ce/Ce~*)_D锆石氧逸度计和(X_(Ce~(4+))~(melt)/X_(Ce~(3+))~(melt))锆石氧逸度计计算得到的波龙、多不杂矿床含矿花岗闪长斑岩体的氧逸度(log(f_(O_2)))分别位于MH(磁铁矿-赤铁矿)缓冲带和FMQ(铁橄榄石-磁铁矿-石英)缓冲带之上,平均值为ΔMH+3.24和ΔFMQ+1.78,前人研究发现多不杂含矿石英斑岩的氧化状态较高,平均ΔNNO+2.4,含矿斑岩体的形成具有较高的氧逸度条件,说明高氧逸度更有利于多龙矿集区斑岩型铜矿成矿。     

江西省村前铜多金属矿床斜长花岗斑岩LA-ICP-MS锆石U-Pb年龄及地质意义

村前铜多金属矿床是产于钦杭成矿带东段的重要的斑岩-矽卡岩矿床,含矿岩体为黑云母斜长花岗斑岩和斜长花岗斑岩,具有多次侵入特点及钙碱性岩石的地球化学特征.本研究采用了LA-ICP-MS技术,首次对含矿的斜长花岗斑岩岩体中的锆石进行了U-Th-Pb同位素分析,获得其成岩年龄为(169.3±1.1 )Ma.这一年龄与钦杭成矿带中德兴花岗闪长斑岩、银山石英斑岩、冷水坑花岗斑岩、桐村花岗斑岩等岩体的年龄十分接近,揭示在钦杭成矿带175～156Ma经历了一次大规模的岩浆侵位与成矿事件,形成了众多与埃达克质或钙碱质花岗岩有关的斑岩-矽卡岩型铜多金属矿床,进一步说明钦杭成矿带在此时期在同一岩浆-动力背景下形成了斑岩-矽卡岩型铜多金属矿成矿系列.     

粤北大宝山矿区花岗闪长斑岩LA-ICP-MS锆石U-Pb年龄及其地质意义

对粤北大宝山钼钨多金属矿区的花岗闪长斑岩进行了锆石阴极发光显微结构观察和LA-ICP-MS锆石微区U-Pb定年.在锆石阴极发光图像中, 两个花岗闪长斑岩样品中的锆石颗粒具有明显的振荡环带, 为典型的岩浆锆石.LA-ICP-MS U-Pb定年结果显示: 大宝山花岗闪长斑岩样品中具岩浆环带锆石区域12个分析点的206Pb/238U加权平均年龄为175.8±1.5 Ma(MSWD=0.037), 船肚花岗闪长斑岩样品中具岩浆环带锆石区域16个分析点的206Pb/238U加权平均年龄为175.0±1.7 Ma(MSWD=0.41).它们的形成时代约175 Ma, 为燕山早期第Ⅰ阶段(180~170 Ma)产物.本次对大宝山矿区花岗闪长斑岩形成时代的准确厘定, 为大宝山和船肚花岗闪长斑岩原本连为一体被后期构造错断的认识提供了新证据, 岩体错断部位是矿区Mo-W矿进一步勘探的重要方向.结合相关研究表明, 其成岩成矿动力学背景与邻区岩体相似, 为南岭地区同一期岩石圈伸展-减薄事件的产物.同时启示我们, 在南岭地区还存在燕山早期第一阶段(180~170 Ma)利于形成Mo-W矿的花岗岩类小岩体未被揭露.      

海南岛高通岭钼矿床赋矿岩体LA-ICP-MS锆石U-Pb年龄、Hf同位素和Ce4+/Ce3+特征

高通岭钼矿床位于海南岛中部的早白垩世—晚白垩世高通岭岩体中,是一个小型热液脉型钼矿床。作者对赋矿围岩黑云母钾长花岗岩进行了岩相学观察、LA-ICP-MS锆石U-Pb定年、锆石Lu-Hf同位素测试和锆石微量元素分析。结果显示:赋矿围岩矿物组合为钾长石(45%~60%)、石英(20%~30%)、斜长石(10%~20%)及黑云母(10%~15%);矿石矿物以辉钼矿为主,矿石类型主要为石英脉型,次为蚀变黑云母钾长花岗岩型和碎裂岩型;高通岭岩体中的锆石,具有清晰的振荡环带,显示其岩浆成因;锆石U-Pb年代学研究获得206U/238Pb加权平均年龄为(102.5±1.8)Ma,锆石的~(176)Hf/~(177)Hf比值为0.282 349~0.282 663,εHf(t)为-12.8~-1.7,二阶段地壳模式年龄(TCDM)为1976~1271 Ma,峰值为1450~1400 Ma,锆石稀土元素配分模式显示高通岭岩体的陆壳源区属性。地表取样的黑云母钾长花岗岩(GTL-03和GTL-04)具有较低Ce~(4+)/Ce~(3+)比值(160左右),反映了较低氧逸度,钻孔取样的黑云母钾长花岗岩具有较高Ce~(4+)/Ce~(3+)比值(平均值377)。高通岭岩体总体上氧逸度较低,暗示其大规模成矿潜力较低。     

粤北大宝山矿区船肚岩体和大宝山花岗斑岩锆石LA-ICP-MS U-Pb年龄及多阶段成矿分析

粤北大宝山矿床矿区出露船肚和大宝山矿化岩体。本文分析了两个岩体矿物组成特征和锆石LA-ICP-MS U-Pb年龄。船肚岩体为似斑状结构,块状构造,主要由似斑状花岗岩、似斑状二长花岗岩及似斑状花岗闪长岩等组成,和云英岩型及矽卡岩型Mo-W矿化紧密共生。大宝山岩体为斑状结构,块状构造,主要由碱长花岗斑岩、普通花岗斑岩、二长花岗斑岩及花岗闪长斑岩组成,矿物组成和船肚岩体的基本相同,和细脉浸染状Mo-W矿化紧密共生。船肚似斑状二长花岗岩和大宝山二长花岗斑岩锆石LA-ICP-MS U-Pb年龄分别为162.1±1.6 Ma,MSWD=2.72和165.8±2.0 Ma,MSWD=1.38。据船肚和大宝山岩体矿物组成基本相同、岩石结构不同及两者锆石Th/U比值不同和U-Pb年龄存在约4 Ma左右时差,提出大宝山矿区在燕山期发生了两阶段岩浆成矿事件,第一阶段岩浆成矿事件发生在166 Ma左右,形成大宝山斑岩型矿床,第二阶段岩浆成矿的形成时间约为162 Ma左右,形成船肚似斑状二长花岗岩及与岩体紧密共生的矽卡岩型和云英岩型矿化;大宝山斑岩体和船肚似斑状岩体是同一岩浆房两次脉动侵入形成的。     

阿尔泰小土尔根铜矿区岩体LA-ICP-MS锆石U-Pb定年及地质意义

小土尔根是近年来阿尔泰诺尔特盆地发现的首例斑岩铜矿床,其成岩成矿年代学的研究可以对矿床模型构建、区域成矿规律的总结提供制约。矿区侵入岩发育,矿化受花岗闪长斑岩控制,少部分赋存在地层中。文章利用LA-ICP-MS锆石U-Pb测年法对矿区岩体进行了成岩年代学研究。含矿花岗闪长斑岩、黑云二长花岗岩和花岗斑岩中锆石的206Pb/238U年龄的加权平均值分别为(401.0±2.9)Ma、(398.1±2.2)Ma和(400.5±2.0)Ma,为早泥盆世同一岩浆侵入活动形成的不同侵入岩。侵入岩年龄结合凝灰岩年龄,将矿区地层划归早泥盆世诺尔特组。含矿花岗闪长斑岩锆石U-Pb年龄限定小土尔根斑岩铜矿床成矿时代略晚于401 Ma,即矿床形成于早泥盆世。     

广东省大宝山钼多金属矿区岩浆岩成岩时代研究

大宝山钼多金属矿区位于南岭成矿带中段。区内主要分布有次英安斑岩、花岗闪长斑岩;钼多金属矿床受NW、E-W、NE等方向断裂组成的构造格架控制,矿体分布与岩浆岩有密切关系。通过对大宝山钼多金属矿区丘坝次英安斑岩和船肚花岗闪长(斑)岩单颗锆石LA-ICP-MS测试,得出丘坝次英安斑岩单颗锆石U-Pb法206Pb/238U表面年龄(419~496 Ma)、花岗闪长(斑)岩单颗锆石U-Pb法206Pb/238U表面年龄(410~489 Ma),反映二者形成时代一致,可能为同一来源岩浆的产物;大宝山强蚀变次英安斑岩锆石SHRIMP U-Pb法206Pb/238U表面年龄有两组,一组为145~168 Ma,另一组为412~420 Ma;认为大宝山钼多金属矿区大面积分布的次英安斑岩和花岗闪长(斑)岩为加里东末期形成的岩浆岩,而紧贴钼多金属矿体分布的岩浆岩为燕山早期岩浆活动形成产物。     

Study on Yanshanian metallogenic granitoids magmatism in Baoshan deposit,southern Hunan ProvinceSCIEI北大核心CSCD

本文对湘南宝山花岗闪长斑岩进行了系统的锆石和磷灰石U-Pb定年、岩石地球化学以及锆石Hf同位素研究,并探讨了宝山花岗闪长斑岩的岩石成因和构造意义。锆石和磷灰石的LA-ICP-MS U-Pb定年显示,宝山花岗闪长斑岩的成岩年龄为160Ma。综合元素和同位素地球化学证据,宝山花岗闪长斑岩的成因可能为新生地壳与古老地壳的混合熔融,同时宝山花岗闪长斑岩中发现的890±20Ma的继承锆石,验证了新元古代新生地壳的参与。磷灰石的主微量元素研究显示花岗闪长斑岩具有较高的氧逸度和Cl含量,Sr/Th比值具有较大变化,而La/Sm比值变化不大等特征,表明形成花岗闪长斑岩岩浆的母岩受到俯冲板片脱水形成的流体交代作用影响。在上述过程中,富含Cl和H2O的流体从板片中释放出来,引发地幔楔熔融,并对矿床中成矿金属元素进行提取。由于古太平洋板块俯冲引发的伸展-减薄运动,在地幔上涌过程中,新元古代新生地壳发生部分熔融,这些高温岩浆底侵老地壳源区,诱发老地壳部分熔融,进而发生了强烈的壳-壳混合作用,产生花岗闪长质岩浆。     

邦铺钼(铜)矿床二长花岗斑岩、黑云二长花岗岩锆石Hf同位素和Ce4+/Ce3+比值

文章对邦铺钼(铜)矿区产出的中新世二长花岗斑岩[(16.23±0.19)Ma]及古新世黑云二长花岗岩[(62.1±1.9)Ma]的锆石进行了微量元素和Hf同位素组成的研究.锆石Hf原位分析表明,邦铺钼(铜)矿区含矿二长花岗斑岩、成矿前黑云二长花岗岩的176Hf/177Hf比值分别为0.282 818～0.282 904...     

黑龙江多宝山斑岩Cu-Mo矿床成岩成矿时代研究

多宝山斑岩型铜(钼)矿床是中国东北地区重要的斑岩型铜(钼)矿床,文章对矿区主要成矿岩体及辉钼矿样品进行了系统的成岩成矿年代学研究。对成矿岩体采用高精度LA-ICP-MS锆石U-Pb测年,获得成矿母岩花岗闪长斑岩的锆石U-Pb年龄为(474.8±4.7) Ma,矿体寄主岩石花岗闪长岩的锆石U-Pb年龄为(478.1±4.1) Ma,以及矿体外围黑云母花岗闪长岩的锆石U-Pb年龄为(483.9±4.5) Ma;矿体辉钼矿的Re-Os同位素模式年龄加权平均值为(475.1±5.1) Ma。测年结果显示,多宝山斑岩铜(钼)矿床形成于早奥陶世。结合含矿地层、矿区岩石组合特征,以及前人研究的岩石地球化学特征,推测多宝山矿床形成于早奥陶世与板块俯冲有关的岛弧环境,说明在区域上寻找类似多宝山的斑岩铜矿应沿早奥陶世多宝山-伊尔斯岩浆岛弧带开展。     

Energy transfer among Pb, Ce and Mn in fluorescent calcite from Kuerle, Xinjiang, China

Natural calcite from Kuerle, Xinjiang, China, shows orange-red fluorescence when exposed to short-wave ultraviolet (UV) light (Hg 253.7 nm). Photoluminescence (PL) emission and excitation spectra of the calcite are observed at room temperature in detail. The PL emission spectrum under 208 nm excitation consists of three bands: two UV bands at 325 and 355 nm and an orange-red band at 620 nm. The three bands are ascribed to Pb²⁺, Ce³⁺ and Mn²⁺, respectively, as activators. The Pb²⁺ excitation band is observed at 243 nm, and the Ce³⁺ excitation band at 295 nm. The Pb²⁺ excitation band is also observed by monitoring the Ce³⁺ fluorescence, and the Pb²⁺ and Ce³⁺ excitation bands, in addition to six Mn²⁺ excitation bands, are also observed by monitoring the Mn²⁺ fluorescence. These indicate that four types of the energy transfer can occur in calcite through the following processes: (1) Pb²⁺ → Ce³⁺, (2) Pb²⁺ → Mn²⁺, (3) Ce³⁺ → Mn²⁺ and (4) Pb²⁺ → Ce³⁺ → Mn²⁺.     

皖南晚中生代花岗闪长岩地球化学:成岩成矿制约

皖南地区是铜、钼、金多金属成矿区,成矿与晚中生代花岗闪长岩类关系密切。近十年来,皖南花岗闪长岩的成因仍然存在分歧。本次报道了皖南花岗闪长岩全岩主、微量元素和锆石原位元素数据。皖南花岗闪长岩(Si O2=64.3%~70.8%)为高钾钙碱性、过铝质岩石,具有相似的埃达克岩特征:高Si O2、Sr/Y(17.1)和(La/Yb)N(14.9)比值,低Yb(1.72×10-6)和Y(18.4×10-6)含量。它们也具有较低Al2O3和Cr(3.40×10-6~10.0×10-6)含量、低Mg#(0.34~0.42)和Nb/Ta(9.6~13.3)值,高K2O和Ba(404×10-6)含量,高K2O/Na2O(0.89~1.55)、Th/La(0.27~0.51)和Th/U(2.79~7.49)比值。锆石原位地球化学特征显示其岩浆源区为低温(锆石Ti-in-zircon温度均值674℃)和高氧逸度(lgfO2集中在-21.4~-9.18,均值-16.4;锆石Ce4+/Ce3+平均值276)的陆壳。这些特征说明皖南花岗闪长岩可能起源于较年轻的加厚下地壳的部分熔融,并经历了斜长石、钾长石和铁镁矿物等结晶分异作用。它们可能形成于与古太平洋板块俯冲密切相关的大陆活动边缘弧至弧后拉张构造转换背景。本区大规模Cu、Mo、Au成矿作用与岩浆的高氧逸度密切相关,而锆石Ce4+/Ce3+可作为矿床勘探一个有效的指标。     

矿物-腐植酸-微生物体系对重金属吸附研究

设施农业中土壤重金属污染问题日趋严重。由于土壤中矿物、腐植酸、微生物等多相组分之间存在交互作用,重金属与土壤单组分体系中所获得的结合机制并不能真实有效地评价其在自然条件下的转化与归趋。本研究以蒙脱石(Mont)和高岭石(Kao)为辽宁蔬菜大棚及农田土壤层状硅酸盐代表矿物,选取胡敏酸(HA)为有机质代表,土著微生物革兰氏阳性枯草芽孢杆菌(Bacillus subtilis,B.s)、革兰氏阴性恶臭假单胞菌(Pseudomonas putida,P.p)为细菌微生物代表,以此三元体系为主要供试蔬菜大棚土壤组分,以Cd~(2+)、Cu~(2+)为目标元素,借助宏观吸附实验,结合X射线衍射(XRD)、衰减全反射-傅立叶变换红外光谱(ATR-FTIR)、扫描电镜(SEM)测试分析了Cd~(2+)、Cu~(2+)在矿物-腐植酸-细菌三元混合物上的吸附机理以及Cd~(2+)、Cu~(2+)在复合体上的结合机制。研究结果表明,蒙脱石/高岭石-腐殖酸、蒙脱石/高岭石-B.s及蒙脱石/高岭石-P.p二元复合体对Cd~(2+)及Cu~(2+)的吸附具有加和性,矿物-腐植酸-微生物三元复合体之间表现为拮抗作用。吸附动力学研究表明矿物、有机质、微生物复合体对重金属的吸附动力学符合准二级动力学模型。体系对Cu~(2+)的吸附能力由强到弱为:B. s P. p Mont/Kao-B. s Mont/Kao-P. p Mont/KaoHA-P.p Mont/Kao-HA Mont/Kao。     

内蒙古阿拉善地区绿色戈壁玛瑙的宝石学特征与致色成因研究

内蒙古阿拉善地区经历数亿年的地质活动,产出颜色丰富且结构致密的戈壁玛瑙。通过常规宝石学测试、偏光显微镜及扫描电镜观察、X射线粉晶衍射、电子探针、红外光谱及紫外-可见光-近红外分光光度计等测试分析方法对绿色戈壁玛瑙的宝石矿物学特征及致色成因进行了深入研究。肉眼观察,阿拉善绿色玛瑙呈深绿色至褐绿色,微透明至不透明,相对密度、折射率、摩氏硬度等均符合石英质玉石的特点。偏光显微镜观察,绿鳞石富集于表层,并向内部呈放射状生长;方解石与石英均为隐晶质结构。扫描电镜观察,绿鳞石呈颗粒状分布于石英及方解石之间。X射线衍射分析结果表明,绿色戈壁玛瑙的物相组成主要为石英、方解石和绿鳞石。电子探针分析结果表明绿鳞石的主要化学组成为SiO₂、FeO、Al₂O₃、K₂O和MgO。红外光谱分析也显示存在绿鳞石对应基团的特征峰。表层绿鳞石在紫外-可见光-近红外分光光度计下显示出Fe²⁺与Fe³⁺的特征光谱,Fe²⁺与Fe³⁺之间的电荷转移是其...     

Local relaxation around [6]Cr 3+ in synthetic pyrope–knorringite garnets, [8]Mg 3 [6](Al 1-X Cr X 3+) 2 [4]Si 3O 12, from electronic absorption spectra

Pyrope-knorringite garnets, Mg₃(Al_1-X Cr³⁺_X)₂Si₃O₁₂ with X=0.25, 0.50, and 1.00, were synthesized between 9 and 16 GPa and 1300 and 1600 °C, using multianvil high-pressure techniques. The garnets with X=0.25 and 0.50 are fine-grained, pink and violet in color. The end-member knorringites with X=1.00 are black when compact and gray when coarse-grained. The fine powder is greenish gray in natural light and pale pink under a tungsten lamp. Powder remission spectra in the wavenumber range 30 000–10 000 cm^–1 on finely powdered crystals were measured by two different methods: (I.) by the use of a small integrating sphere for small samples or (II.) microscope-spectrometric measurement using diffusely reflected radiation from a 45° illuminated microsample. Both methods yielded similar diffuse reflectance spectra. The following crystal-field parameters of ^[6]Cr³⁺ were determined for garnets with X=0.25, 0.50, 1.00: 10 Dq=17 856, 17 596, 17 286 cm^–1; and B=654, 677, 706 cm^–1; nephelauxetic ratio =(B_field/B_free)= 0.71, 0.74, 0.77. The -values indicate decreasing covalency of the Cr–O bond with increasing Cr content. The 10 Dq value for together with the mean Cr–O distance in end-member knorringite, 1.96 Å (Novak and Gibbs 1971), were used to calculate from the spectral data, local mean Cr–O distances (Langer 2001a) as a function of composition. The results indicate relatively strong local site relaxation with a value of =0.77.     

Chromium and vanadium impurities in natural green euclase and their relation to the color

Natural specimens of green gemological euclase (chemical formula BeAlSiO₄(OH)) from Brazil were investigated by electron paramagnetic resonance (EPR) and optical absorption. In addition to iron-related EPR spectra, analyzed recently in blue and colorless euclase, chromium and vanadium-related EPR spectra were also detected in green euclase. Their role as color causing centers is discussed. The results indicate that Cr³⁺ ions substitute for Al³⁺ ions in the euclase structure. The EPR rotation patterns of Cr³⁺ with electron spin S = 3/2 were analyzed with monoclinic spin Hamiltonian leading to the parameters of g _xx , g _yy and g _zz equal to 2.018, 2.001 and 1.956 and electronic fine structure parameters of D = −8.27 GHz and E = 1.11 GHz, respectively, with high asymmetry ratio E/D = 0.13. For the vanadium-related EPR spectra the situation is different. It is concluded that vanadium is incorporated as the vanadyl radical VO²⁺ with electron spin S = 1/2 with nearly axial spin Hamiltonian parameters g_zz = 1.9447, g _xx  = 1.9740 g _yy  = 1.9669 and axial hyperfine interactions due to the nuclear spin I = 7/2 of the ⁵¹V isotope leading to A _zz  = 502 MHz, A _xx  = 150 MHz and A _yy  = 163 MHz. The green color of euclase is caused by two strong broad absorption bands centered at 17,185 and 24,345 cm⁻¹ which are attributed to the ⁴A_2g → ⁴T_2g, ⁴T_1g transitions of Cr³⁺, respectively. Vanadyl radicals may introduce some absorption bands centered in the near infrared with tail extending into the visible spectral range.     

Experimental Study on the Solubility of Cr^2 in Olivine,Orthopyroxene and Spinel Solid Solutions

Experiments have been performed on the system MgO-SiO2-Cr-O at 0-2.88 GPa and 1100-1450℃,focusing on the stability of Cr^2 in olivine(O1),orthopyroxene(Opx) and spinel(Sp) and its partitioning between these phases.Analytical reagent grade chemicals,MgO,SiO2,Cr2O3.and Cr were used to make starting mixtures.Excess Cr(50%) was then added in these mixtures to ensure that the resultant phases were in equilibrium with the metal Cr.Flux of BaO B2O3(%) was added for facilitating experimental equilibrium and crystal growth.Cr was used as capsule material.All phases in the product were identified by X-ray and analyzed by electron microprobe,The contents of CrO in the different phases(O1,Opx and Sp)were calculated according to stoichiometry.The obtained results of calculation indicate that Cr^3 in Ol and Opx is negligible.The experimental results show;(a) with increasing temperature and decreasing pressure,Cr^2 solubility in Ol,Opx and Sp increases;(b) with in creasing temperature,the partitioning coefficient of Mg and Cr^2 between Ol and Opx decreases,that between Opx and Sp increases,and that between Ol and Sp remains almost unchanged;(c) the effect of pressure on all partitioning coefficients is negligible.     

溶出珊瑚砂中Ca~(2+)、Mg~(2+)的动力学实验研究及其影响因素

通过改变固液比、摇床转速、珊瑚砂粒径、温度、溶液pH值及溶液含盐量等参数,对珊瑚砂在水溶液中溶出Ca~(2+)、Mg~(2+)进行了实验,以探讨溶出过程中的动力学规律和影响因素。实验结果表明,珊瑚砂中Ca~(2+)、Mg~(2+)溶出量随反应时间逐渐增大;摇床转速越快、固液比越大、温度越高、溶液pH值越低,Ca~(2+)、Mg~(2+)溶出量越大;当珊瑚砂粒径为2.36~4.75 mm、溶液含盐量为100 mg/L时,Ca~(2+)、Mg~(2+)溶出量最大。统计分析表明,摇床转速、温度及溶液p H值均对珊瑚砂溶出有显著影响,但溶液p H值影响最大。珊瑚砂在水中的溶出过程符合收缩核内扩散模型,表明控制整个溶出过程反应速率的决定因素是内扩散速率;在15~40℃时,珊瑚砂在纯水中溶出Ca~(2+)、Mg~(2+)的活化能分别为78.07和74.91 k J/mol。     

40Ar/39Ar evidence for the timing of Paleoproterozoic gold mineralisation at the Sandpiper Deposit,Tanami region,northern Australia

At the Sandpiper gold deposit in the Tanami region of northern Australia sericite is intimately intergrown with arsenopyrite in gold-bearing quartz veins and breccias, suggesting sericite crystallisation synchronous with gold-bearing fluid flow. This ore-stage sericite yields a ⁴⁰Ar/³⁹Ar plateau age of 1785 ± 32 Ma (2σ including both analytical and systematic uncertainties). Recalculation using revised and more precise values for the ⁴⁰K decay constants and the age of the Fish Canyon Sanidine standard shifts the age to 1794 ±12 Ma (2σ including all known uncertainties). Given the possibility of post-mineralisation isotopic resetting this age can be conservatively interpreted as a minimum constraint on the timing of gold deposition although, given local geological relationships and estimates for the argon retentivity of white mica, we consider complete isotopic resetting to be unlikely. The preferred interpretation is, therefore, that the sericite ⁴⁰Ar/³⁹Ar age indicates the timing of gold mineralisation. Thesericite age accords with a limited dataset of ²⁰⁷Pb/²⁰⁶Pb xenotime ages of ca 1800 Ma from other gold deposits in the Tanami region, interpreted as mineralisation ages. The agreement between independently derived ages from several gold deposits lends support for a widespread gold-mineralising event at ca 1800 Ma in the Tanami region.