吉林通化集安蛇纹石质玉的矿物成分与成因分析

吉林通化集安地区发现了储量较大的蛇纹石质玉石矿床.X射线荧光光谱分析(XRF)显示蛇纹石质玉石中Si O2含量为35.21%~37.18%,Mg O 46.94%~49.72%,Fe O/Fe2O3之比在0.174~0.685之间.XRD分析显示在0.733 nm、0.366 nm和0.250 nm处存在有利蛇纹石的特征衍射峰.集安蛇纹石质玉主要矿物为利蛇纹石,并常含有镁橄榄石.红外光谱显示在3 650~3 700 cm-1、950~1 100 cm-1、400~700 cm-1存在有特征的利蛇纹石吸收峰.本玉石矿床属区域变质型蛇纹石矿床,利蛇纹石应为橄榄石在低温条件下水热蚀变的产物.     

波伏棱（Povlen）型羟基纤蛇纹石的谱学研究

波伏棱型羟基纤蛇纹石是波伏棱型纤蛇纹石矿物的新变种,本文报导它的吸收光谱、红外光谱、穆斯堡尔谱、电子顺磁共振谱和核磁共振谱。 研究表明,吸收光谱是Fe~(3 )和Fe~(2 )的晶场跃迁以及Fe~(2 )→Fe~(3 )的荷移跃迁引起的;红外光谱是OH和Si-O的伸缩振动、OH转动以及Mg-O和Si-O的弯曲振动引起的;穆斯堡尔谱是Fe~(2 )_(八面体)、Fe~(3 )_(八面体)和Fe~(3 )_(四面体)引起的;电子顺磁共振谱是Mn~(2 )_(八面体)、Fe~(3 )_(八面体)和Fe~(3 )_(四面体)引起的;核磁共振谱是管道水,镁八面体和硅氧四面体上的OH引起的;矿物加热到825℃时,结构开始破坏并出现镁橄榄石相。 此外,本文还解释了该蛇纹石颜色的本质,阐明了上述过渡金属离子和OH在该矿物中的结构环境。     

阿克塞红柳沟纤蛇纹石矿物学特征研究

在对阿克塞红柳沟温石棉矿床的地质特征分析的基础上,采用XRF、XRD、FT-IR、SEM、TG-DTA等分析测试方法对4个纤蛇纹石样品进行了化学成分、晶体结构、谱学特征、显微形貌与理化性质研究。结果表明:纤蛇纹石样品的主要化学组成为SiO2、MgO,其次含有Al2O3、Fe2O3及少量的NiO等类质同象组分,为典型的斜纤蛇纹石结构,内外羟基伸缩振动和Si-O伸缩振动吸收峰尖锐、分裂明显,纤维形态表现为柔韧的丝状,结构破坏温度在650~700℃,酸蚀量在43.67%~59.89%之间,碱蚀量在2.72%~7.01%之间。矿床地质特征和纤蛇纹石的矿物学特征表明该矿床形成后遭受后期的地球化学作用破坏程度低,与纤蛇纹石共生的矿物较简单,纤蛇纹石纤维表面结构较完善。     

碱度对水热合成纤蛇纹石纳米管的影响研究

为克服天然纤蛇纹石纳米管在量子组装应用上存在的不易提纯、易被伴生矿物堵塞、管径不均等缺点,以活性MgO和纳米SiO2为原料,采用水热法在不同碱度下合成了系列纤蛇纹石样品.时合成样品的X射线衍射(XRD)、傅立叶红外光谱(FTIR)以及扫描电镜(SEM)分析表明,在200℃.pH值大于13的条件下反应60 h以上能够合成结晶度比较完善的纤蛇纹石;碱度的提高有利于纤蛇纹石氢氧镁石层和硅氧四面体层的生长,并促使两者结合更为紧密,晶胞参数b0值增大,结构层更易卷曲,纤蛇纹石的纤维管状结构更加完善,结晶度提高,纤维的晶体轮廓更加清晰,直径更为均一,长度增加;最后确认在200℃.pH 13.8,反应60 h条件下合成纤蛇纹石纳米管的直径约50 nm.长度多在600nm以上,长度上优于前人的合成.     

蛇纹石族矿物及其热转变产物的红外光谱研究

本文报道了蛇纹石族矿物及其热转变产物的红外光谱。在室温下斜纤蛇纹石,正纤蛇纹石,叶蛇纹石和利蛇纹石都具有各自的特征光谱。在结构资料基础上,我们解释了它们之间的光谱差异。无疑,红外光谱是区分各种蛇纹石矿物的有效手段。 样品加热到600—700℃时,3680cm~(-1)羟基带消失,这表明在该温度下蛇纹石矿物完全脱羟。与此同时,光谱中出现橄榄石870cm~(-1)的最强带和一个宽带1000cm~(-1),这说明蛇纹石已部分地转变为晶质橄榄石和形成一个无定形的中间相。800℃时,1060cm~(-1)新带的出现标志着顽火辉石的生成。在所有加热样品的光谱中都没有发现SiO_2吸收带,故可认为,在蛇纹石的热转变过程中没有出现SiO_2相。     

不同亚类硅酸盐矿物的中红外光谱学特征

利用热红外发射光谱研究了不同亚类硅酸盐矿物镁橄榄石、透闪石、蛇纹石和钠长石的红外发射光谱特征。在120oC时,通过对400～1650 cm-1的红外波段进行积分计算,发现硅酸盐矿物中镁橄榄石的发射率最高,可达到0.988,钠长石最低为0.947。硅酸盐矿物在850～1300cm-1区间均产生宽的低发射带,该发射带与硅氧四面体层中(Si,Al)-O的伸缩振动相关;在470 cm-1左右则形成相对尖锐的低发射带,与硅氧四面体层中(Si, Al)-O的弯曲振动相关。从岛状、链状、层状到架状硅酸盐矿物由于Si O2聚合程度依次增加,最强发射谷的位置依次向高频方向偏移,说明硅氧四面体中Si-O伸缩振动带的位置受到了n(Si)/n(O)比值的制约。此外,在辐射能量谱里,镁橄榄石、透闪石、蛇纹石和钠长石的最强辐射谷范围趋于变宽,依次为115、162、225和247 cm-1,反映了吸收的辐射能增加。综上可推测,硅酸盐矿物强的发射率可能与硅氧四面体中Si-O的振动模式、Si O2的聚合度、辐射能量谱中最强辐射谷的波长范围有关。     

山西省河曲县铺沟铝土矿中勃姆石的矿物学特征及其成因探讨

本文对山西省河曲县铺沟铝土矿中的勃姆石进行了偏光显微镜、X射线粉末衍射、红外光谱、扫描电镜鉴定,研究了其矿物学特征。勃姆石晶体形态呈菱形、柳叶状及鳞片状。X射线衍射特征峰有:d020=6.109,d120=3.160,d=051=1.863,d200=1.848,d220=1.769,d080=1.529;晶胞参数为a0=3.690,b0=12.162,c0=2.866;红外光谱反映的特征谱带是3300cm-1和3078cm-1。文章还对其成因进行了探讨,认为主要是由胶体晶化及高岭石脱硅转变而来。     

吉林省集安安绿玉矿物学特征

安绿玉产于吉林省集安地区,为胶状隐晶质蛇纹石矿物集合体,属岫玉一个新品种。安绿玉的化学成分与蛇纹石的理论化学组成接近。x射线、红外吸收光谱、电子显微镜、穆斯堡尔谱和吸收谱研究表明:安绿玉主要由利蛇纹石组成,含有一定量正纤蛇纹石。利蛇纹石为片状、正纤蛇纹石为管状、纤维状集合体。安绿玉具多种颜色,它取决于铁的含量、价态和位置,含Fe~3+呈黄色系列,而Fe~(2+)→Fe~(3+)电荷转移吸收呈蓝色系列。利蛇纹石的Fe~(2+)、Fe~(3+)在八面体M_1和M_2位置上分布是无序的。文中还论述了玉石特征及其与成分和结构的关系。     

红外光谱在铁镁硅酸盐矿物类质同象研究中的应用

本文通过对柘榴石、辉石、角闪石和云母等铁镁质矿物的化学成分、光学性质和其它物性及红外吸收光谱的研究,试图找出它们的内在联系,以便用于研究矿物的类质同象变化规律。所测的矿物红外吸收光谱为中红外4000～400cm~(-1)波段的谱带特征,一般认为该波段主要是表现为硅酸盐中阴离子团的振动区。 从1、2图中可以看出所测矿物的谱带特征,铁镁硅酸盐谱带基本可分为三个波段,第一波段1100—800cm~(-1)据G.R.Hunt,J.W.Salisbury(1974),提出的硅酸盐光谱振动模式,该波段均为O—Si—O,Si—O—Si的非对称伸缩振动区。所以它们共同特点     

四川石棉蛇纹石猫眼热相变的Raman光谱和XRD研究

采用Raman光谱和X射线粉晶衍射(XRD)方法对四川蛇纹石猫眼的热相变过程和产物进行的研究表明,蛇纹石猫眼热相变的最终产物为镁橄榄石和顽火辉石。加热到500℃,蛇纹石猫眼的结构稳定;700℃,时,镁橄榄石的拉曼特征峰824cm^-1和854cm^-1出现,同时出现非晶质顽火辉石686cm^-1和341cm^-1附近的包络峰;800～900℃时,镁橄榄石的含量和结晶程度增强。晶质顽火辉石相出现,但强度较弱。1000℃时,镁橄榄石的含量明显降低。1100℃时,顽火辉石的含量和结晶程度显著增加。     

广西陆川蛇纹石玉的岩相结构及成矿机理

应用外束质子激发X射线荧光光谱法、X射线衍射、激光拉曼光谱、扫描电子显微镜等无损分析技术,对广西陆川蛇纹石玉的成分、物相和结构进行分析。X射线衍射结果显示样品的衍射峰主要位于0.724、0.456、0.362、0.248、0.153和0.150 nm处,表明陆川蛇纹石玉主要矿物成分是蛇纹石,同时伴生方解石矿物与蛇纹石形成穿插交织结构。成矿机理分析表明,陆川蛇纹石玉是由白云质大理岩热液交代作用形成的,和广东的信宜玉均属于富镁碳酸盐型蛇纹石。拉曼光谱显示叶蛇纹石的特征峰位于229、376、457、686和1046 cm-1处,纤蛇纹石的特征峰位于228、345、386、624、690和1102 cm-1处,通过激光拉曼光谱可以快速区分陆川蛇纹石玉中纤蛇纹石和叶蛇纹石两种不同结构的蛇纹石亚种。     

Origin and nature of sungulite

Sungulite is variety of serpentine finely to coarsely flaky, white with a silky luster. The term should be applied to coarse tabular serpentine (antigorite) in pseudomorphs on vermiculite. It is formed out of vermiculite and is surficial in origini occurring as a gradual replacement of vermiculite in lower parts of ancient weathering crusts of magnesian rocks with ferro-magnesian micas. It appears that the genetic relationships between kaolinite and halloysite are quite similar to those between sungulite and chrysotile. — J. J. Finney.     

三斜水钠锰矿层间阳离子交换作用的拉曼谱学

水钠锰矿为自然界中常见的锰氧化物矿物,其离子交换作用及结构转变理解尚不深刻,矿物表征手段较为局限.为探究水钠锰矿的离子交换特性以及结构转变在拉曼光谱上的反映,利用MnSO₄和NaOH合成了三斜晶系的Na型水钠锰矿,进行了NH₄+、K+、Mg2+、Ca2+、Ba2+、Co2+、Zn2+的离子交换实验,使用ICP-OES、XRD、拉曼光谱等手段对离子交换水钠锰矿进行表征.拉曼光谱分析表明,570~585 cm-1与640~655 cm-1两个锰氧八面体伸缩振动模式的相对强度及570~585 cm-1附近拉曼峰峰位指示水钠锰矿的结构对称型;570~585 cm-1拉曼峰强度大、振动频率高指示三斜对称型.280 cm-1与500 cm-1附近的拉曼峰是层间离子种类的识别标志.水钠锰矿层间若为Na+、K+、Mg2+、Ca2+、Ba2+等碱金属、碱土金属离子,则在280 cm-1附近存在1个峰值,500 cm-1存在2个分立的峰值;其他种类的层间离子仅500 cm-1处有1个孤峰,指示层间离子排列无序.      

Foliation development in serpentinites, Glenrock, New South Wales

At Glenrock, near the southern end of the Peel Fault System, two fault zones are delineated by mélanges in which serpentinite is the main rock type.Protogranular and mylonitic textures are present in relicts of the parent peridotite and in blocks of massive pseudomorphic serpentinite that are surrounded by schistose serpentinite. In schistose serpentinite, the earliest foliation (S₁) is defined, microscopically, by the parallel alignment of platy and fibrous serpentine minerals (lizardite and chrysotile) and by trains of magnetite and flattened serpentine pseudomorphs after olivine and pyroxene. It is considered that the schistosity formed perpendicular to the direction of maximum shortening, under conditions in which lizardite and chrysotile were ductile, but antigorite was not, by breakdown of pre-existing serpentine minerals and new growth of lizardite and chrysotile.Post-s₁ foliations (S₂andS₃) superficially resemble crenulation cleavages in the field but, microscopically, show evidence of shear displacement and are referred to as microshear sets. They probably originated in the ductile-brittle transitional field of serpentine behaviour (Raleigh and Paterson, 1965).     

In Situ Oxygen Isotope Determination in Serpentine Minerals by SIMS: Addressing Matrix Effects and Providing New Insights on Serpentinisation at Hole BA1B (Samail ophiolite,Oman)

The ability to constrain the petrogenesis of multiple serpentine generations recorded at the microscale is crucial for estimating the extent and conditions of modern versus fossil serpentinisation in ophiolites. To address matrix bias effects during oxygen isotope analysis by SIMS, we present the first investigation analysing antigorite in the compositional range Mg# = 77.5–99.5 mole %, using a CAMECA IMS‐1280 secondary ion mass spectrometer. Spot‐to‐spot homogeneity is ≤ 0.5‰ (2s) for the new antigorite reference materials. The relative bias between antigorite reference materials with different Mg/Fe ratios is described by a second‐order polynomial, and a maximum difference in bias of ~ 1.8‰ was measured for Mg# ~ 78 to 100. We observed a bias up to ~ 1.0‰ between lizardite and antigorite attributed to their different crystal structures. Orientation effects up to ~ 1‰ were observed in chrysotile. The new analytical protocol allowed the identification of oxygen isotope zoning up to ~ 7‰ in serpentine minerals from two serpentinites recovered from an area of active serpentinisation in the Samail ophiolite. Thus, in situ analysis is capable of resolving isotopic heterogeneity that may directly reflect changes in the physical and chemical conditions of multiple serpentinisation events in the Samail ophiolite.     

Serpentinization: a review

The common alteration assemblage produced by serpentinization of ultramafic rocks is: lizardite, chrysotile, magnetite±brucite±antigorite. Lizardite-chrysotile serpentinites are more common than antigorite; the presence of antigorite indicates that the serpentinite has undergone prograde metamorphism or that the periootite was serpentinized in a higher P,T regime than lizardite and chrysotile. The iron subsitution into serpentine minerals and brucite is a function of temperature at low f_O2, with increased temperature enhancing magnetite formation. The presence of awaruite and native Fe are strong evidence for a locally very reducing environment. Isotopic studies have shown a wide variety of origins for the fluids involved in serpentinization. The increased boron content of serpentinized rocks when compared to boron contents of the parent ultramafic body indicates a possible sea water origin for the fluids. Serpentinization takes place under both constant volume and constant chemical composition conditions. The factors in evaluating the importance of the two processes for an individual serpentinite are: (1) determination of the mineral assemblage and its paragenesis, (2) the structural and tectonic relationship of the ultramafic body to its country rock, (3) fluid access to the rock in duration and amount, and (4) timing of serpentinization - before, during or after emplacement into the crust.     

Hydrothermal altered serpentinized zone and a study of Ni-magnesioferrite–magnetite–awaruite occurrences in Wadi Hibi,Northern Oman Mountain: Discrimination through ASTER mapping

Economic important minerals and ore deposits are common in hydrothermal altered serpentinized zone. Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) satellite sensor is capable of discrimination of such hydrothermal mineralized zone and detection of hydrothermal altered minerals. In the present study, the hydrothermal altered serpentinized harzburgites of Wadi Hibi area of Northern Oman Mountains have been discriminated by using ASTER VNIR–SWIR spectral bands by image processing methods and the occurrences of Ni-magnesioferrite–magnetite–awaruite in the rocks are studied. The color composite RGB image developed using ASTER spectral bands 8, 4 and 1, mapped well the occurrence of weathered peridotites by pale green to dark blue in colors and discriminated the hydrothermally altered serpentinized rocks by pale brown to dark blue colors due to the strong absorption of OH and Mg–OH molecules that occurred in the serpentine minerals of the rocks in the study area. The ASTER band ratios 4/7, 4/1, and 2/3 × 4/3 RGB images studied are capable of discrimination of hydrothermal mineralized areas more clear by pale blue to purple colors due to the strong absorption of such hydroxyl bearing serpentine minerals. The studied image processing methods are evaluated by applying to the region of Wadi Sarami situated in the Semail ophiolite (Oman). In addition to that, the occurrence of serpentine minerals namely, lizardite and antigorite in the hydrothermally altered serpentinized region are detected qualitatively and quantitatively using Spectral Angle Mapper (SAM) supervised classification image processing method and studied.The interpreted images are verified in the field and checked for the occurrences of minerals including Ni-magnesioferrite, magnetite, pentlandite and awaruite and are confirmed through laboratory studies. Petrographic study of serpentinized harzburgites shows that the rocks consist predominantly of antigorite and lizardite serpentines, olivine and have the opaque minerals assemblage of Ni-magnesioferrite + magnetite + awaruite + pentlandite developed during serpentinization of the rock. The occurrences of such minerals are confirmed by XRD, electron microprobe analyses and spectral measurements in the laboratory.ASTER sensor proved its capability in discriminating the hydrothermal altered serpentinized zone and detecting the mineral occurrences and thus the study recommends the technique to the exploration geologists, scientists and mining geologists for mapping of such rocks and minerals in the similar arid region.     

Polysomatism,polytypism, defect microstructures,and reaction mechanisms in regularly and randomly interstratified serpentine and chlorite

High-resolution (HRTEM) and analytical electron (AEM) microscopic evidence for a polysomatic series based on regular interstratifications of serpentine (amesite) and chlorite (clinochlore) are reported from an altered skarn in Irian Jaya. The assemblage includes regular interstratifications of one clinochlore and two (2:1; three structural variants), three (3:1), and four (4:1) amesite composition 1:1 layers as well as randomly interstratified serpentine and chlorite. The order of abundance of regularly interstratified minerals is 1:1>2:1>4:1>3:1. Atomic-resolution images, image simulations, and comparison between calculated and observed diffracted intensities verify the proposed 1:1 and 2:1 structures and reveal details of their defect microstructures. AEM data show that compositions are linear combinations of the associated amesite and clinochlore. The 1:1, 2:1, 3:1, and 4:1 minerals occur both as discrete sub-micron crystals and as domains within serpentine or chlorite. Some crystals of the 2:1 phase were sufficiently large for study by X-ray precession and powder methods. Crystals of the regularly interstratified 2:1, 3:1, and 4:1 phases are usually bent. High-resolution images reveal that, within polygonal segments, the layers commonly exhibit a few degrees of curvature with segments separated by antigorite-type offsets. Deformed chlorite crystals are probably replaced by interstratified minerals during an aluminum metasomatic event. Al may have been deposited from sulfuric acid-rich solutions when they interacted with calcite and dolomite to form the anhydrite-rich corona around the phyllosilicate-rich region of the core. The interstratified chlorite (clinochlore composition) suggests aluminum addition by selective conversion of a sub-set of the chlorite layers to amesite. Defect microstructures suggest that crystals of regularly interstratified material grew by direct structural modification of preexisting chlorite. Regular interstratifications may form in response to thermally controlled limits on Al solubility in chlorite and heterogeneities in the distribution of Al-rich solutions during metasomatism. Regularly interstratified minerals coexist with randomly interstratified serpentine/chlorite, chrysotile, antigorite, lizardite, and several amesite and chlorite polytypes. Tentative chlorite and amesite identifications include one-layer (b=97°, probably IIbb), one-layer (b=90, possibly Ibb), two-, and three-layer chlorites, and 2H₁ (but possibly 1M or 1T), rhombohedral (3R or 6R), and twelve-layer (Tc; non standard) serpentine polytypes. The complex phyllosilicates attest to rampant chemical and structural disequilibrium.     

蛇纹石族矿物的红外光谱特征及其研究

蛇纹石族矿物的红外吸收光谱,早在50年代末期已有报道,70年代以来,特别是偏振光的红外光谱技术应用后,对蛇纹石族矿物的红外光谱与晶体结构之间的关系,有了进一步的研究,对谱带的归属也作了阐述^[2,3]。     

盔犀鸟头胄工艺品的宝石学及谱学特征

对市场上出现的盔犀鸟头胄工艺品及其拼合制品、仿制品,在宝石显微镜下放大观察,采用扫描电子显微镜、傅里叶变换红外光谱仪、紫外一可见光谱仪、激光拉曼光谱仪等大型分析仪器进行测试,探究其物质组成、生长结构、颜色成因以及鉴定方法。结果表明,盔犀鸟头胄整体表现为层状鳞片生长结构,头胄工艺品的黄色基体中普遍发育近平行条带生长结构,红色圆斑与黄色基体呈渐变过渡关系;红外光谱表现为酰胺特征吸收谱带,表明角蛋白为头胄主要成分;特征的紫外一可见吸收光谱与拉曼光谱均标志着类胡萝卜素的存在,且类胡萝卜素是头胄的主要呈色原因。拼合工艺品的红色圆斑具有清晰边界并可见拼合缝隙,红外光谱显示红色圆斑为人造树脂材料。仿制品的黄色基体内部可见气泡,红外光谱揭示其整体均为人造树脂。