Structure Refinement of Cs-rich Na-Li Beryl and Analysis of Its Typomorphic Characteristics of Configurations

1 Introduction Natural beryl is an accessory mineral mainly in pegmatite, partly in some highly diffractionated granite or metamorphic rocks, with the crystal shapes beingprismatic, or occasionally tabular. For tabular beryl found in pegmatite it is believed that the tabular configuration is connected with alkali metals (Bieus, 1960; Wang et al., 1981) and geneses of the tabular configuration have been reported before. In recent years, tabular beryl has been found in the Xuebaoding W-Sn-Be d…     

新疆阿尔泰伟晶岩中绿柱石拉曼光谱特征研究——以可可托海3号脉与阿祖拜328、528号脉为例

本文对新疆可可托海3号伟晶岩脉中的绿柱石与阿祖拜328、528号伟晶岩脉中的宝石级绿柱石开展拉曼光谱对比研究,获得以下主要结论: ① 阿祖拜328、528号伟晶岩脉中宝石级绿柱石以富含Ⅰ型H₂O为特征,可可托海3号脉早期形成的结构带(Ⅰ-Ⅱ带)中绿柱石以及相对富H₂O岩浆体系中形成的绿柱石(Ⅳ带)以存在Ⅰ型H₂O为主,演化程度相对较高,岩浆体系中结晶的结构带(Ⅲ带)以及岩浆-热液过渡阶段体系形成的结构带(Ⅴ带)中绿柱石以含有Ⅱ型H₂O为特征; ② 在可可托海3号脉以及阿祖拜328号、528号脉绿柱石矿物中均发现冰晶石矿物包体,指示伟晶岩岩浆含有较高的F含量;③ 绿柱石通道水类型(Ⅰ型H₂O、Ⅱ型H₂O)及相对比例,是伟晶岩岩浆-热液演化过程及其形成条件的响应,在相对氧化的岩浆体系中主要形成绿柱石矿物,而相对还原的富H₂O岩浆体系更有利于海蓝宝石形成.     

The positions of H+, Li+ and Na+ impurities in beryl

Electron Paramagnetic Resonance (EPR) measurements show that Li⁺ impurities are located at two different positions in beryl, one in the crystal lattice and the other in the crystal channel. The position of the Li⁺ impurity in the lattice is generally assumed to be at the site of a missing Be²⁺ ion. It is shown that this is not the case, but that the Li⁺ ion is located in a tetrahedron formed by the oxygens of one side of the Be tetrahedron and the nearest oxygen in the channel ring. This Li site has the coordinates (0.423, 0.344, 0.167) and can only be occupied when the neighbouring Be site is empty. There are four such sites around every Be tetrahedron at the distance of 1.46 Å from the Be site. The distance from the Li site to the oxygens of the Li tetrahedron is 1.84 Å. This compares favourably with the much smaller distance of 1.65 Å in the Be tetrahedron. Protons in beryl are trapped at or near these Li sites. Na⁺ is known to be located at the 2b position at the center of the silicate rings, where it is stabilized by one water molecule located at each of the two surrounding 2a sites. This is also the position of Li⁺ in the beryl channel. It is found that the presence of Na⁺ in the ring of six oxygens reduces the radius of this ring. The Na⁺ impurity has also been supposed to be located at position 2a alone and at 2b stabilized by only one water molecule. It is now proposed that Na⁺ and H₂O are located together in the Al–Be plane when only one water molecule is associated with Na⁺. The water oxygen is located at or near 2a and Na is closer to the Be site in tetrahedral beryl and closer to the Al site in octahedral beryl. It is proposed that the water protons are also located in the Al–Be plane, which would mean that there exists a third type of water in beryl. The origin of protons and OH^? ions in beryl is discussed and it is suggested that the plugs in the beryl channels are CO ₃ ^2? ions. Diffusion of OH^? ions and natural radiation may have led to the creation of NO₃ and the blue colour of Maxixe beryl.     

含铁绿柱石的改色机制研究

含铁绿柱石经γ射线辐照或特定温度热处理,可因铁价态的改变引起颜色发生相应变化。处理前后的吸收光谱和顺磁共振谱研究表明,辐作用使隧道位的Ｆｅ＾２＋氧化Ｆｅ％３＋,八一位上的Ｆｅ＾３＋还原为Ｆｅ＾２＋,热处理使隧道位及八面体位Ｆｅ＾３＋均还原为Ｆｅ＾２＋。     

伟晶岩绿柱石矿物学及其通道水氢同位素研究进展

自然界绿柱石存在三个类质同象系列,即“八面体”绿柱石（ｃ／ａ＝０．９９１￣０．９９６）,“正常”绿柱石和“四面体”绿柱石。绿柱石矿物精细结构研究表明,二价离子置换八面体中Ａｌ,Ｌｉ置换四面体中Ｂｅ,而碱离子被绿柱石通道所容纳,用于补偿低价阳离子置换Ａｌ八面体和Ｂｅ四面体引起的电价不足。伟晶岩绿柱石通常含有〉１．６ｗｔ％的通道水,而包裹体中流体仅为０．１５ｗｔ％左右。室温下绿柱石通道中存在１型和Ⅱ     

四川平武板状绿柱石矿物学特征及板状成因

在综合该区绿柱石产出背景的基础上,从围岩蚀变、矿物共生组合、矿物标型形态和绿柱石测温测压等方面确定平武绿柱石矿床是气成高温浅成石英脉型矿床。文中对绿柱石矿物进行了湿法化学分析、X射线粉晶衍射分析、微形貌分析,研究了该区绿柱石的形态、物性、化学成分及类质同象特征,确定该区绿柱石为板状晶形的含铯钠锂绿柱石,碱金属平均质量分数为2.412%(Li2O+Na2O+K2O+ Rb2O+Cs2O)。板状含碱绿柱石一般发育在伟晶岩中,气成高温热液矿床中产出板状含碱绿柱石极为罕见。在以上工作基础上,从绿柱石形成的内因和外因两方面探讨了绿柱石的板状成因。     

平武板状绿柱石{0001}晶面的溶蚀像特征与晶体生长

板状绿柱石产于花岗岩云英岩化边部或晶洞壁的白云母-钠长石-绿柱石-水晶的矿物组合中,钠长石呈自形晶,绿柱石的洁净度与透明度相对较差。晶体测量表明,晶体的单形晶面发育依次为c{0001}→s{11 2-1}→p{10 1-1}→m{10 1-0}→v{21 3-1}、n{45 9-4}、a{11 2-0}。微分干涉显微镜(DIC)及扫描电镜(SEM)研究表明:各单形晶面上生长纹(微形貌)反映面网结构的对称性,c{0001}单形晶面上的六边形溶蚀坑(50～170μm)是由平行晶体C轴的各单形晶面生长层从晶体中心向外叠堆组成,层生长机理制约晶体生长全过程,平行双面(c)的生长层较薄(5～8μm)且较稳定,六方双锥(s)生长层较厚且圆滑,六方柱(m)生长层由晶体中心往外其厚度由厚逐渐变薄(12～20μm),台间隔由窄变宽。晶体溶蚀是从面网密度最大的c{0001}开始,溶蚀面积依平行双面(c)、六方双锥(s)单形晶面由大变小,六方柱(a)、复六方双锥(v、n)单形晶面因面网密度小而未受到溶蚀。据矿物共生组合、流体包裹体均一法测量与拉曼光谱(LRS)分析表明板状绿柱石是在中–高温(303℃)、过饱和度较大、成矿介质的钠长石化发育且热动力环境相对稳定的条件下形成,气液包裹体主要由H2O、CO2及微量CH4、N2组成,CO2及微量CH4、N2可能与碳酸盐围岩有关。     

中沙群岛近海表层沉积物中的火山灰及其对构造环境的响应

南海中沙近海表层沉积物的轻组分(粒径为63~125μm)中主要包括有褐色火山玻璃、无色火山玻璃以及火山渣等3种火山灰类型。在硅碱图(TAS)及Al2O3、FeO*、MgO、CaO、Na2O、K2O对SiO2的变化趋势图中可以判断,本区可能存在双峰式火山活动,褐色火山玻璃代表中-基性端元,而无色火山玻璃代表酸性端元。无色火山玻璃与褐色火山玻璃具有共同的岩浆源区,结晶分异可能是源区岩浆演化的主要方式。这种双峰式火山活动暗示火山活动源区处于大陆拉张减薄环境,支持西沙海槽是一个正在活化的伸展大地构造现象这一观点,同时肯定基于地球物理学和岩石学研究资料所提出的海南地幔柱的存在。     

绿柱石中铁离子的晶格占位及致色作用

绿柱石族宝石颜色丰富,一直是市场上重要的宝石品种。几十年来,国内外学者对不同颜色绿柱石的致色机理及改色工艺开展了广泛的研究。铁离子作为重要的致色过渡金属离子之一,其价态调控是绿柱石改色工艺的关键,所以铁离子的价态、晶格占位和对应的致色作用也一直是绿柱石研究的焦点。铁离子被认为可能存在于绿柱石中的铝氧八面体Al³⁺格位、硅氧四面体Si⁴⁺格位、铍氧四面体Be²⁺格位、结构通道2a或2b位和晶格间隙6g位等位置,是蓝、绿或黄等颜色绿柱石的主要致色元素。本文通过对绿柱石的晶体结构、铁离子的核外电子排布和晶格占位等方面文献资料的梳理及综合分析,认为Fe²⁺和Fe³⁺分别对蓝色和黄色绿柱石的呈色起着主导作用。当Fe²⁺和Fe³⁺处于晶格中不同位置时致色作用的具体差异,仍有待于进一步研究。     

辐照条件下绿柱石通道中顺磁配合物的ESR行为

四川平武贫铁富碱型无色绿柱石通道中主要存在碱氢化物（NaH)、[Fe2(OH)4]^2 多聚合离子及OH自由基，在电子辐照作用下，通道中顺磁配合物的结构、带电性质及化学键易发生转型、裂解和变价，并形成自旋浓度不等的[H^0]i心（裂距为500G,g值分别为2．175，1．8774的二重超精细结构线）、[Fe^3 ]OH(g=2.0031)和[Fe4^3 ]s(g=4.3172)等辐照损伤心。[Fe^3 ]OH心属一种有效的电子陷阱，其热稳定性大于[Fe4^3 ]s心。绿柱石杂质铁离子的占位方式，与成矿物理、化学条件及成矿流体的pH值密切相关。由电子辐照作用而导致杂质离子价态的转变，属一种可逆的动态平衡过程。