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1.
四川沐川地区峨眉山玄武岩出露广泛,开采技术条件好。采集11件玄武岩岩芯样品进行地球化学、薄片鉴定和拉丝试验等测试分析,从化学成分、岩石组构和拉丝工艺等3个方面对其进行了纤维用玄武岩原矿的初步评价。结果显示,玄武岩样品w(SiO2)为47.15%~51.35%,w(Al2O3)为10.52%~14.30%,w(Fe2O3)为2.42%~7.56%,w(FeO)为6.02%~9.26%,w(CaO)为4.20%~8.88%,w(MgO)为3.26%~5.25%,全碱w(K2O+Na2O)为3.29%~5.66%,w(TiO2)为2.78%~4.94%。玄武岩类型包括致密块状玄武岩、含杏仁状玄武岩和杏仁状玄武岩,均属碱性—亚碱性过渡系列岩石,岩石结构主要为拉斑玄武结构和粗玄结构。6件致密块状玄武岩均能连续拉丝成功,其化学成分稳定和析晶上限温度为1 270℃,应优考虑其作为连续纤维用玄武岩原矿;2件含杏仁玄武岩均能连续拉...  相似文献   

2.
玄武岩纤维是以天然玄武岩为生产原料,高温熔融后经漏板拉丝制备而成的纤维。玄武岩纤维中TiO2、MgO组分含量较低,但对纤维形成的影响不可忽略。根据峨眉山玄武岩中TiO2、MgO含量不同的斜斑玄武岩和致密玄武岩进行拉丝试验,从玄武岩纤维成丝率、纤维断裂强度、熔制性能等分析,结合已有研究成果对玄武岩中TiO2、MgO含量进行讨论。结果表明,连续玄武岩纤维矿石中的TiO2、MgO可增强玄武岩纤维的热性能和化学性能,在一定范围内TiO2含量增加、MgO含量减少,可提高玄武岩纤维的稳定性和成丝率,增强纤维断裂强度。在现有的工艺条件下,根据不同类别的玄武岩,可将连续玄武岩纤维矿石中TiO2含量扩大到4%,增加矿石原料的选取范围。  相似文献   

3.
对采自贵州省赫章县不同地区的16件致密状和3件杏仁状玄武岩进行了拉丝试验,从化学成分、矿物成分、拉丝温度、试验转速、析晶上限温度等方面分析了拉丝成功的影响因素,讨论了本区玄武岩作为生产连续玄武岩纤维原矿石的可能性,同时探讨了生产连续玄武岩纤维的拉丝作业温度.结果 表明,赫章县不同地区19件玄武岩,16件拉丝成功、3件拉丝失败;16件致密状玄武岩有15件拉丝成功、3件杏仁状玄武岩有2件拉丝失败.该区致密状玄武岩化学成分和矿物成分绝大部分符合连续纤维用玄武岩标准,具有重要的开发利用价值;利用本区致密状玄武岩生产连续纤维过程中,拉丝作业温度应高于1350 ℃.  相似文献   

4.
超大陆裂解是当今地学研究最前沿课题.通过研究塔里木南缘铁克里克构造带前寒武纪变质火山岩的岩石化学特征、微量元素特征、稀土元素特征及Sm-Nd同位素特征, 探讨古塔里木板块的中元古代大陆裂解构造事件.该套变质火山岩组合下部以变质酸性火山岩(流纹岩夹部分晶屑凝灰岩)为主, 夹少量玄武岩, 上部为玄武岩夹少量条带状大理岩.基性火山岩w(SiO2)为42.34%~49.55%, w(Na2O+K2O)为2.63%~8.81%.下部玄武岩w(Na2O)/w(K2O)值为0.54~1.5, 为钾玄岩系列, 稀土总量高, 且轻稀土富集, 平均w(La)n/w(Yb)n值为3.45, δ(Eu)为0.69~0.91, 具弱至中等的Eu负异常, 微量元素具有碱性板内玄武岩特征; 上部玄武岩w(Na2O)/w(K2O)为5.11~17.89, 为拉斑系列, 轻重稀土没有明显分异, δ(Eu)在0.81~1.13之间, 基本没有Eu异常, w(La)n/w(Yb)n平均为1.69, 配分曲线与大洋拉斑玄武岩一致, 微量元素显示LILE(如Rb、Ba、Th)富集, HFSE与大洋拉斑玄武岩一致.岩石地球化学反映从早到晚由碱性-钙碱系列逐渐向拉斑系列演化.在上部玄武岩中获得(1 200± 82.3)Ma的Sm-Nd等时线年龄.认为该套变质火山岩记录了古塔里木板块在中元古代大陆裂解的构造过程.   相似文献   

5.
黄从俊  李明辉 《地质与资源》2023,(3):301-310+300
通过野外和镜下岩相学观察,结合主、微量元素地球化学方法,研究了四川省广安市邻水县西天超大型纤维用玄武岩矿床的地质特征,分析了矿石工业指标和矿床成因.结果表明:矿床位于川东褶皱带华蓥山背斜东翼,矿体呈似层状赋存于上二叠统峨眉山玄武岩组(P3β)地层中,矿石储量约1 594×104t,达超大型规模;主量元素地球化学特征表明,西天玄武岩岩浆属高钛、高钾钙碱性-钙碱性系列;稀土元素、微量元素地球化学特征与区域内高钛峨眉山玄武岩及OIB型玄武岩特征相似;西天玄武岩为峨眉山大火成岩省的外带组成部分,形成于板内构造环境,岩浆演化来源于OIB型源区且基本未受地壳物质混染,为地幔热柱成因的产物;矿床中的柱状节理玄武岩、块状玄武和气孔状玄武岩可用于纤维拉丝生产.  相似文献   

6.
云南上沧二叠纪枕状玄武岩位于峨眉山大火成岩省内带底部。该玄武岩全岩SiO2含量为49.36%~51.36%,TiO2含量为1.28%~1.91%,MgO含量为6.08%~10.79%,Mg#值为53~69,Al2O3含量为13.91%~16.31%,Na2O含量为1.59%~3.72%,K2O含量较低,为0.18%~0.76%,并且Na2O/K2O比值较高,为4.27~10.48,属拉斑系列玄武岩。具有右倾斜型稀土元素配分模式,重稀土和部分高场强元素与N-MORB接近,轻稀土和部分大离子亲石元素介于N-MORB和上地壳之间。(La/Sm)N比值大多数低于2.0(1.4~2.2),(Ce/Yb)N比值介于2.2~3.4之间,明显低于OIB,不具有OIB的地球化学特征,在Th/Hf-Ta/Hf构造环境判别图解中位于陆缘裂谷玄武岩区域,推测上沧枕状熔岩是古特提斯洋俯冲到扬子板块边缘形成的初始裂谷扩张的产物。  相似文献   

7.
东昆仑成矿带是我国西部重大成(找)矿潜力的贵金属-有色金属成矿带。野外调查期间,对东昆仑东段都兰县诺木洪南下石炭统哈拉郭勒组(C1h)杏树沟金矿(化)点进行了年代学及围岩地球化学研究。通过高精度LA-ICP-MS锆石微区原位U-Pb同位素测年,获得金矿(化)点的石英钠长斑岩 206Pb/238U 年龄加权平均值为243.4±1.9 Ma,确定金矿(化)发生在早三叠世。地球化学分析表明,杏树沟金矿(化)点围岩(安山玄武岩)具有高Al2O3、Na2O,低TiO2、K2O的特征。在Zr/TiO2-Nb/Y图解中全部样品均落入安山玄武岩区,TFeO/Mg-SiO2图解中全部样品均落入拉斑系列区域中,属于拉斑系列玄武岩。稀土和微量元素显示其富集LREE、LILE和部分HFSE,Nb、Ta、Nd、Zr、Hf相对亏损,REE表现为LREE/HREE明显分离的分配模式,从多种判别图解综合分析,认为该套火山岩形成于大陆裂谷环境中。  相似文献   

8.
根据岩棉用玄武岩矿床地质勘查工业指标要求,开展了六盘水市淤泥河地区岩棉用玄武岩矿床整装勘查,采样分析了岩棉用玄武岩矿石SiO_2、Al_2O_3、Fe_2O_3等化学成分,评价(332)+(333)内蕴经济资源量93亿吨。本文总结了研究区岩棉用玄武岩矿床地质特征及矿石加工技术性能指标要求,分析了玄武岩纤维产品性能和市场竞争优势,研究区岩棉用玄武岩资源市场潜力极大,指出了研究区玄武岩资源开发意义。  相似文献   

9.
四川盆地华蓥山玄武岩出露于茅口组顶部,夹于龙潭组底部的杂色泥岩、页岩之间,岩性为灰黑色粗玄岩,底部致密块状,顶部见气孔—杏仁状构造。TAS图解显示玄武岩属于碱性与偏碱性过渡带上的拉斑玄武岩系列,TiO2含量介于2.92%~3.63%之间,Ti/Y值为465~567,属于高钛玄武岩(HT)。岩石LREE/HREE=3.25~3.96,轻稀土略富集,具有右倾平滑型稀土分配模式。华蓥山玄武岩与云南宾川,贵州赫章等地峨眉山玄武岩的地球化学特征相似,反映了相同的幔源性质。结合野外地质特征,认为华蓥山玄武岩应属峨眉地幔柱的一部分,是沿着华蓥山基底断裂发生裂隙式喷发的产物。研究区的高钛玄武岩Ce/Yb介于22.65~27.93,与前人报道的高钛玄武岩Ce/Yb比值范围基本一致,处于石榴石稳定区与尖晶石稳定区的过渡带,Th/Ta、Nb/U、La/Ta等比值反映出岩石受壳源物质的混染程度很低,可能是地幔柱轴部的产物。  相似文献   

10.
东昆仑造山带诺木洪郭勒早古生代火山活动   总被引:3,自引:1,他引:2  
诺木洪郭勒一带发育早古生代火山岩, 可明显分为2种类型: 一类为基性火山岩组合, 岩石主要为具枕状构造的玄武岩, SiO2碱度均较低, 为拉斑系列玄武岩, 稀土、微量元素特征及构造环境判别显示其形成于洋中脊的构造环境; 另一类为中基性火山岩组合, 火山岩岩石类型复杂, 熔岩和火山碎屑岩均较发育, 熔岩成分从基性到中酸性均有, 火山岩SiO2成分变化较大, 既有亚碱性, 又有碱性, 亚碱性系列岩石多属钙碱性系列.稀土、微量元素特征及构造环境判别其形成于火山弧的环境.   相似文献   

11.
福建天马山—牛头山新生代玄武岩及其火山作用   总被引:4,自引:1,他引:4  
林友坤 《岩石学报》1992,8(4):376-385
  相似文献   

12.
南天山造山带南缘发育大量的下二叠统火山岩。地球化学指标显示南天山南缘西段拜城县宿相厄肯沟出露的下二叠统小提坎立克组玄武岩为拉斑玄武岩(里特曼指数δ=2.93)。 该套岩石低FeOT、MgO和全碱(Na2O+K2O),高CaO和Al2O3,相对高钠,低钾; Rb、K、U和Ba 等大离子亲石元素富集; 稀土配分曲线整体协调一致,为向右缓倾的曲线,轻稀土元素(LREE)相对富集; 微量元素配分型式呈"驼峰状"; 玄武岩的母岩浆经历了以单斜辉石为主的分离结晶作用和强烈的陆壳混染作用。同位素组成 143 Nd/144 Nd =0.512 849±0.000 005, 87 Sr/86 Sr =0.706 845±0.000 014; -10<εNd(t)<0,且εSr(t)>0,模式年龄TDM 为1.463 279 765 Ga。 结合区域地质资料表明,小提坎立克组玄武岩形成于板内伸展环境,具有主动裂谷作用性质,说明南天山造山带南缘当时处于碰撞后伸展背景。  相似文献   

13.
“三江”义敦岛弧带玄武岩喷发序列与裂谷—岛弧转化   总被引:2,自引:1,他引:2  
岩石-构造组合是恢复古板块构造历史的最有效手段之一,同时是表征古板块边界与板内环境的最重要的地质证据。本文拟从岩石-构造组合角度,通过对义敦岛弧带玄武岩,特别是前岛弧期玄武岩喷发序列、岩石组合、地球化学特征和其形成背景的研究,试图从较深层次上揭示岩浆-构造内在联系,探索义敦古岛弧的形成与发展。  相似文献   

14.
广西大新地区辉绿岩地质地球化学、年代学特征及其意义   总被引:4,自引:0,他引:4  
广西大新地区位于华南板块南华活动带右江褶皱系西大明山凸起,大新凹断束,那岭—俸屯褶断地垒的北端,辉绿岩脉沿断裂呈北西向零星分布。该区产有铀矿、铅锌矿等矿产资源。前人在进行矿床成因等研究时没有将辉绿岩脉与矿床的形成联系起来。通过研究辉绿岩的地质、地球化学和年代学特征,对二者的关系进行了探讨,取得如下认识:①该区辉绿岩分布受北西向断裂控制,并且遭受了后期变质作用和蚀变作用,使其主要由高岭石、蛇纹石、绿泥石等蚀变矿物组成,局部地段有铀矿化。②辉绿岩的SiO2含量变化较大,主要由后期硅化导致。Fe2O3,MgO,CaO及FeO与SiO2呈明显的负相关,碱质程度(Na2O+K2O)较贫,K2O/Na2O比值较大,为钙碱性系列。微量元素富集高场强元素Ta,Nb,Zr,Hf,及大离子亲石元素Rb,U,Th,Ba,而亏损Sr,构造环境判别为板内玄武岩(WPB)。稀土元素球粒陨石标准化分布型式图呈右倾,稀土元素总量较高,轻稀土较重稀土富集,无明显Eu异常。③辉绿岩的锆石U-Pb年龄总体为90 Ma左右,形成于晚白垩世。④辉绿岩脉与该区矿产资源的形成有一定关系。  相似文献   

15.
甘孜-理塘结合带作为三江特提斯造山带与松潘-甘孜造山带的重要组成部分,发育大量的洋岛-海山岩石组合,洋岛玄武岩的存在标志着洋盆已发育成熟的洋壳.木里地区的洋岛-海山岩石组合由"基性火山岩+碳酸盐岩"构成,对基性火山岩的地球化学特征分析表明:基性火山岩SiO2含量为40.17%~49.19%,TiO2含量1.77%~4.86%,Al2O3含量9.67%~15.39%,MgO含量3.85%~17.75%,全碱含量(K2O+Na2O)0.87%~6.33%,属碱性玄武岩系列.稀土总量∑REE值较高,为106.21×10-6~378.83×10-6,(La/Yb)N比值为9.23~39.41,为轻稀土富集型,Eu、Ce无异常,配分模式为右倾型.微量元素表现出大离子亲石元素Rb、Ba、Th、K富集,而亏损高场强元素Nb、Zr.稀土元素及微量元素特征与标准洋岛型玄武岩相近,源区为软流圈地幔石榴石橄榄岩,且部分经历了岩浆结晶分异,形成于洋岛台地环境.玄武岩的锆石U-Pb定年结果为218.96~221.71 Ma,表明洋岛型玄武岩形成于晚三叠世中期.  相似文献   

16.
The North Qilian orogenic belt is a typical plate suture zone, which is studded with numerous different sizes of fragments of micro-continental crust consisting of pre-Sinian metamorphic rocks and the North Qilian orogenic belt provides important study carrier for studying the pre-orogenic tectonic process of the North Qilian. The relatively complete volcanic-clastic-carbonate rocks formation of Zhulongguan Group, Changchengian System, Mesoproterozoic are distributed in the Kawa-Qiqing area, Western North Qilian orogenic belt. Geochemical characteristics of the Aoyougou Group basalts in the North Qilian indicated that the contents of major element were relatively stable, high K2O contents(4.27%~6.07%), TFe2O3(10.49%~13.01%),TiO2(1.96%~2.90%)and middle MgO(5.37%~6.71%,Mg# 48~51), CaO(2.57%~5.51%)content. Thus, the Aoyougou Group basalts belong to potassium alkaline basalt. The contents of Cr and Ni of the basalts decreased with the decreasing of Mg#, and there was a positive correlation between CaO and CaO/Al2O3, Furthermore, the Eu anomaly of samples was slightly negative, high contents of high field strength elements (HFSE, Nb, Ta, Ti), and the ratios of Gd/Yb(2.5~3.0), Zr/Y(8.6~10.2), Ta/Yb(0.96~1.23), Ti/Yb(5 074~6 021), Zr/Yb(81~97), Ce/Nb(1.87), Zr/Nb(6.41)indicated that the Aoyougou Group basalts had obvious OIB-type magmatic affinity. In combination with the regional geological background, the study results showed that Aoyougou Group alkaline basalt generated from deep enrichment mantle similar to the source of OIB, with fractional crystallization of olivine and monoclinic pyroxene and a certain degree of contamination of continental crust in the process of magmatism, formed in the background of continental rift, might response to the Proterozoic Columbia supercontinent rifting, which further provides important petrological evidences for the relationship between North China Craton rifting events and Columbia supercontinent rifting during Proterozoic.  相似文献   

17.
The Emeishan continental flood basalt (ECFB) sequence in Dongchuan, SW China comprises a basal tephrite unit overlain by an upper tholeiitic basalt unit. The upper basalts have high TiO2 contents (3.2–5.2 wt.%), relatively high rare-earth element (REE) concentrations (40 to 60 ppm La, 12.5 to 16.5 ppm Sm, and 3 to 4 ppm Yb), moderate Zr/Nb and Nb/La ratios (9.3–10.2 and 0.6–0.9, respectively) and relatively high Nd (t) values, ranging from − 0.94 to 2.3, and are comparable to the high-Ti ECFB elsewhere. The tephrites have relatively high P2O5 (1.3–2.0 wt.%), low REE concentrations (e.g., 17 to 23 ppm La, 4 to 5.3 ppm Sm, and 2 to 3 ppm Yb), high Nb/La (2.0–3.9) ratios, low Zr/Nb ratios (2.3–4.2), and extremely low Nd (t) values (mostly ranging from − 10.6 to − 11.1). The distinct compositional differences between the tephrites and the overlying tholeiitic basalts cannot be explained by either fractional crystallization or crustal contamination of a common parental magma. The tholeiitic basalts formed by partial melting of the Emeishan plume head at a depth where garnet was stable, perhaps > 80 km. We propose that the tephrites were derived from magmas formed when the base of the previously metasomatized, volatile-mineral bearing subcontinental lithospheric mantle was heated by the upwelling mantle plume.  相似文献   

18.
Trevor H. Green  John Adam 《Lithos》2002,61(3-4):271-282
The solubility of Ti- and P-rich accessory minerals has been examined as a function of pressure and K2O/Na2O ratio in two series of highly evolved silicate systems. These systems correspond to (a) alkaline, varying from alkaline to peralkaline with increasing K2O/Na2O ratio; and (b) strongly metaluminous (essentially trondhjemitic at the lowest K2O/Na2O ratio) and remaining metaluminous with increasing K2O/Na2O ratio (to 3). The experiments were conducted at a fixed temperature of 1000 °C, with water contents varying from 5 wt.% at low pressure (0.5 GPa), increasing through 5–10 wt.% at 1.5–2.5 GPa to 10 wt.% at 3.5 GPa. Pressure was extended outside the normal crustal range, so that the results may also be applied to derivation of hydrous silicic melts from subducted oceanic crust.

For the alkaline composition series, the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure but is unchanged with increasing K content (at fixed pressure). The P2O5 content of the alkaline melts at apatite saturation increases with increased pressure at 3.5 GPa only, but decreases with increasing K content (and peralkalinity). For the metaluminous composition series (termed as “trondhjemite-based series” (T series)), the TiO2 content of the melt at Ti-rich mineral saturation decreases with increasing pressure and with increasing K content (at fixed pressure). The P2O5 content of the T series melts at apatite saturation is unchanged with increasing pressure, but decreases with increasing K content. The contrasting results for P and Ti saturation levels, as a function of pressure in both compositions, point to contrasting behaviour of Ti and P in the structure of evolved silicate melts. Ti content at Ti-rich mineral saturation is lower in the alkaline compared with the T series at 0.5 GPa, but is similar at higher pressures, whereas P content at apatite saturation is lower in the T series at all pressures studied. The results have application to A-type granite suites that are alkaline to peralkaline, and to I-type metaluminous suites that frequently exhibit differing K2O/Na2O ratios from one suite to another.  相似文献   


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