首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
The cathodoluminescence analyses of the trigonal carbonates calcite and dolomite have been applied intensively in sedimentary petrology for a long time and the properties of these minerals are well-known, but much less attention has been paid to aragonite. In this study, the cathodoluminescence behaviour and the trace element composition of natural and synthetic aragonite have been studied employing trace element analyses (proton induced X-ray emission) and luminescence spectroscopy. Aragonite doped with Mn2+ has been synthesized in a NH4+–Mg2+–Ca2+–Cl− solution in contact with a CO2–H2O–NH3 atmosphere. The low effective distribution coefficients indicate a rapid growth of the crystals of millimetre size which occurred within hours or days. The natural aragonite samples contain Mn, Fe and Sr in different concentrations. The Mn-bearing aragonites exhibit a bright green luminescence which is caused by a strong emission band at 575 nm with a half-width of about 84 nm. The luminescence intensity shows a strong positive correlation with Mn in aragonite when Fe and Mn do not exceed 2000 p.p.m. The intensity is depressed if the concentration of these elements exceeds the critical values. In the shell of a recent Unio sp., the luminescence intensity deviates from the linear correlation, although the trace element contents are not too high; this is probably an effect of quenching by organic material between the crystallites of the biogenic aragonite.  相似文献   

2.
以钛酸正丁酯\[Ti(OBu)4\]为前驱体,通过水热法制备了稀土Tb3+掺杂的TiO2粉体样品,并利用激发光谱（PLE）、光致发光（PL）光谱对制得的样品进行了光谱研究。结果表明：水热法制备的掺杂有Tb3+的TiO2粉体在室温下可以得到Tb3+的特征发射,并且Tb3+离子的发光强度与制备条件有关,当反应温度为125℃、反应时间为72 h、Tb3+的掺杂体积分数为12%时发射峰的强度达到最大。  相似文献   

3.
A combination of high resolution cathodoluminescence-spectroscopy (HRS-CL=high resolution spectroscopy of cathodoluminescence emission) with spatial resolving trace element analyses (PIXE=proton induced X-ray emission) is used to establish a method for the quantitative determination of the Mn-content of diagenetic and hydrothermal dolomites using the measurements of peak areas of Mn-activated CL emission bands. This method takes into account the overlap of the CL broad bands of Mn2+ in the Mg- and the Ca-lattice-position of dolomite. There is a linear correlation between the peak areas and Mn concentration up to approx. 1000–1500 ppm. Thus, CL spectroscopy allows a determination of Mn concentrations below the abilities of PIXE (10–15 ppm) to less than 1 ppm by extrapolation of this linear relation.

Up to an Fe-content of approx. 2000 ppm, no quenching effect of Fe on this linear relationship occurs. However, Fe-contents above 2000 ppm result in a decrease of Mn-induced luminescence. Even at Fe-concentration >25,000 ppm spectroscopy reveals that Mn-activated CL of dolomite is not entirely extinguished.  相似文献   


4.
Atmospheric precipitation samples were collected in the Bohemian Karst (30 km SW from Prague, Czech Republic) at six localities in the vicinity of the limestone-quarry Čertovy schody during years 1996–2003. Samples were analyzed for major components (Na+, K+, Mg2+, Ca2+, F−, Cl−, NO3−, HCO3−, SO42−) and trace metals (Cu, Mn, Fe, Zn, Pb, Be, As, Sr, Cd, Al, Cr). Deposition fluxes were calculated from more than 10 000 elemental analyses of samples collected monthly. The fluxes of monitored substances show temporal and spatial variability. The most marked attribute is the strong affection by local emission sources confirmed by the investigation of seasonal variability, temporal trend and correlation analysis.  相似文献   

5.
We report here for the first time, the occurrence of sapphirine+quartz assemblage in textural equilibrium from quartzo-feldspathic and pelitic granulites from southern India. The sapphirine-bearing rocks occur as layered gneisses associated with pink granite within massive charnockite in Rajapalaiyam area in the southern part of Madurai Block. Sapphirine occurs in three associations: (i) fine-grained subhedral mineral associated with quartz enclosed in garnet, (ii) intergrowth with Al-rich orthopyroxene (up to 9.7 wt.% Al2O3), and (iii) in symplectitic intergrowth with orthopyroxene (Al2O3= 5.9–6.7 wt.%) and cordierite surrounding garnet. The sapphirine in association with quartz is slightly magnesian (XMg = 0.79–0.80) and low in Si content (1.55–1.56 pfu) as compared with those associated with orthopyroxene and cordierite (XMg= 0.77–0.79, Si = 1.59–1.63 pfu). The sapphirine+quartz assemblage suggests that the granulites underwent T>1050 °C peak metamorphism. Cores of porphyroblastic orthopyroxene in the sapphirine-bearing rocks shows high-Al2O3 content of up to 9.7 wt.%, suggesting T = 1040–1060°C and P = 8 kbar. FMAS reaction of sapphirine+quartz→garnet+sillimanite+cordierite indicates a cooling from sapphirine+quartz stability field after the peak ultrahigh-temperature metamorphism. Slightly lower temperature estimates from ternary feldspar and sapphirine-spinel geothermometers (T = 950–1000°C) also support a post-peak isobaric cooling. Corona textures of orthopyroxene+cordierite (±sapphirine), orthopyroxene+sapphirine, and cordierite+spinel around garnet suggest subsequent decompression. The sapphirine-quartz association and related textures reported in this study have important bearing on the ultrahigh-temperature metamorphism and exhumation history of the Madurai Block as well as on the tectonic evolution of the continental deep crust in southern India.  相似文献   

6.
Summary ?Sheet silicates of the serpentine–kaolin-group (serpentine, kaolinite, dickite, nacrite, halloysite), the talc–pyrophyllite-group (talc, pyrophyllite), the smectite-group (montmorillonite), and illite (as a mineral of the mica-group) were investigated to obtain information concerning their cathodoluminescence behaviour. The study included analyses by cathodoluminescence (CL microscopy and spectroscopy), electron paramagnetic resonance (EPR), X-Ray diffraction (XRD), scanning electron microscopy (SEM) and trace element analysis. In general, all dioctahedral clay minerals exhibit a visible CL. Kaolinite, dickite, nacrite and pyrophyllite have a characteristic deep blue CL, whereas halloysite emission is in the greenish-blue region. On the contrary, the trioctahedral minerals (serpentine, talc) and illite do not show visible CL. The characteristic blue CL is caused by an intense emission band around 400 nm (double peak with two maxima at 375 and 410 nm). EPR measurements indicate that this blue emission can be related to radiation induced defect centres (RID), which occur as electron holes trapped on apical oxygens (Si–O centre) or located at the Al–O–Al group (Al substituting Si in the tetrahedron). Additional CL emission bands were detected at 580 nm in halloysite and kaolinite, and between 700 and 800 nm in kaolinite, dickite, nacrite and pyrophyllite. Time-resolved spectral CL measurements show typical luminescence kinetics for the different clay minerals, which enable differentiation between the various dioctahedral minerals (e.g. kaolinite and dickite), even in thin section. Received December 3, 2001; revised version accepted February 27, 2002  相似文献   

7.
采用弹性填料微孔曝气生物修复方法净化受污染的某饮用水源,探讨了天然水体环境温度变化对生物除NH4+-N作用效果的影响.结果表明,水体环境温度对生物修复工艺除NH4+-N作用影响很大.水温越高,生物修复工艺除NH4+-N效果越好.在较低水环境温度下,水温变化对生物修复工艺除NH4+-N作用效果影响最大;在日常水体温度下,水温变化对生物修复工艺除NH4+-N作用效果影响最小;在水体温度较高的条件下,水温变化对生物修复工艺除NH4+-N作用效果影响较小.  相似文献   

8.
《Sedimentary Geology》2006,183(3-4):261-268
Xenotime and zircon in heavy mineral separates of siliciclastic sediments can easily be distinguished by means of cathodoluminescence (CL). All shades of bright blue, yellow and grey to white colours have been reported for zircon while only bottle green to greenish yellow colours have been found in xenotime in heavy mineral separates of Lower Buntsandstein samples as well as in two samples from crystalline rocks from Bahia (Brazil) and the Karpaty Mts. (Slovakia). The CL-spectra of both minerals are commonly dominated by narrow emission bands of rare earth elements, especially Dy3+. The two different crystal lattices induce differences in the intensity ratios of the emission lines that are thought to be the reason for the different CL-colours. Additionally, intrinsic broad bands that may occur in the CL-spectra of zircon are missing in the xenotime spectra. The possibility to distinguish minerals with similar optical properties underlines the large potential of cathodoluminescence in sedimentary petrology.  相似文献   

9.
本文通过沉积环境分析,X射线衍射、扫描电镜、同位素及阴极发光分析,讨论了甘溪泥盆系观雾山组白云石的晶体形态及大小、有序度、碳酸钙克分子含量,同位素特征及阴极发光特征与形成条件的关系。中晶白云岩及细晶白云岩分别产于生物层及潮坪环境,为成岩早期地下淡水与海水混合白云岩化作用的产物。低的碳酸钙克分子含量,中-弱的阴极发光强度及低的δ18O、δ13C值。微晶白云岩形成于泻湖环境。白云石具他形粒状晶,差的有序度,高的碳酸钙克分子含量,强的阴极发光强度及高的δ18O、δ13C值,为准同生期高Mg2+/Ca2+值卤水交代碳酸钙软泥形成。  相似文献   

10.
Micro-X-ray absorption near-edge structure (XANES) analysis was employed to determine the content of ferric iron in minerals formed in ultrahigh-pressure (UHP) eclogites. It is observed that omphacite and phengite contain significant amounts of Fe3+/Fetot (0.2–0.6), whereas only very low contents are present in garnet (Fe3+/Fetot=0.0–0.03), the latter being consistent with results from stoichiometric charge-balance calculations. Furthermore, considerable variations in the Fe3+/Fetot ratios of omphacite and phengite are observed depending on the textural sites and local bulk chemistry (eclogite and calc-silicate matrix) within one thin section. The oxidation state of isofacial minerals is thus likely to depend on the local fluid composition, which, in the studied case, is controlled by calcareous and meta-basic mineral compositions. These first in-situ measurements of ferric iron in an eclogite sample from the Dabie Shan, E China, are used to recalculate geothermobarometric data. Calculations demonstrate that the temperature during UHP metamorphism was as high as 780 °C, about 80–100 °C higher than previously estimated. Temperatures based on charge balance calculations often give erroneous results. Pressure estimates are in good agreement with former results and confirm metamorphism in the stability field of diamond (43.7 kbar at 750 °C). These P–T data result in a geothermal gradient of ca. 6 °C/km during UHP metamorphism in the Dabie Shan. However, accounting for ferric iron contents in geothermobarometry creates new difficulties inasmuch as calibrations of geothermometers may not be correctable for Fe3+ and the actual effect on Mg–Fe2+ partitioning is unknown. The present study further shows that micro-XANES is a promising technique for the in situ determination of ferric iron contents without destroying the textural context of the sample: a clear advantage compared to bulk methods.  相似文献   

11.
白云石化是碳酸盐典型的成岩作用类型之一,中-下奥陶统鹰山组浅海碳酸盐岩是塔河地区重要的含油气储层,普遍发育多种类型的白云石化作用。本文针对塔河地区鹰山组灰岩中沿缝合线分布这一特定类型的白云石化进行了研究。岩石学基础上的阴极发光分析、86Sr/87Sr比值以及δ13C-δ18O 的研究表明,这种类型的白云石化发育于相对还原的浅埋藏成岩环境,孔隙中的残留海水是主要的白云石化流体来源,碳酸盐矿物(主要是高镁方解石)稳定化过程中释放的Mg2+ 可能是白云石化主要的物质来源,而埋藏过程中逐渐升高的温度一定程度上也促进了白云石化的发生。成岩流体及Mg2+ 有限的供给量限制了白云石化作用的整体规模。显微结构与岩石物性分析表明,该类白云石化对储层物性参数的绝对贡献相对有限,但可能成为小规模油气运移以及深部热流体活动的潜在通道。  相似文献   

12.
A series of granitoids from Proterozoic to Cenozoic age occurred in the western Kunlun orogenic belt, Xinjiang, northwestern China. Several intrusions such as the West Datong (Middle Caledonian age), North Kuda (Late Caledonian age) and Kuzigan, Karibasheng, Zankan (Himalayan age) plutons have shoshonitic affinity. Their rock assemblages include (quartz) monzodiorite–(quartz) monzonite–quartz syenite (Middle Caledonian) or monzonitic granite–granite (Late Caledonian) or biotite (monzonitic) granite–diopside granite–diopside syenite (Himalayan). Generally, biotite is iron–phlogopite, with some eastonite and high Mg/(Mg+FeT) and Fe3+/Fe2+ ratio. Amphibole is mainly edenitic hornblende and magnesian hastingsitic hornblende, with some edenite and higher Mg/(Mg+FeT) and Fe3+/Fe2+ ratio. The rocks show SiO2 contents of 52.77–71.85% and high K2O+Na2O (mostly >8%, average 9.14%), K2O/Na2O (mostly >1, average 1.50) and Fe2O3/FeO (0.85–1.51, average 1.01) and low TiO2 contents (0.15–1.12%, average 0.57%). Al2O3 contents (13.01–19.20%) are high but variable. The granitoids are prominently enriched in LILE, LREE and volatiles such as F. However, the studied shoshonitic granitoids among the three intrusive periods also show differences in isotopic compositions and trace element concentrations, suggesting their different geneses: the origin of the West Datong pluton is probably related to the involvement of subducted oceanic crust sediments into the mantle source; the North Kuda and Himalayan plutons could have been generated by partial melting of subducted oceanic crust sediments or metasediments of thickened continental lower crust in the process of late-orogenic slab break-off or lithospheric thinning.  相似文献   

13.
The strongly peraluminous and P-rich, protolithionite and zinnwaldite leucogranites from Podlesí, western Krušné Hory Mts., Czech Republic, contain accessory zircon with extraordinary enrichment of several elements, which constitute trace elements in common zircon. Elements showing a not yet reported anomalous enrichment include P (up to 20.2 wt.% P2O5; equivalent to 0.60 apfu, formula calculated on the basis of 4 oxygen atoms), Bi (up to 9.0 wt.% Bi2O3; 0.086 apfu), Nb (up to 6.7 wt.% Nb2O5, 0.12 apfu), Sc (up to 3.45 wt.% Sc2O3; 0.10 apfu), U (up to 14.8 wt.% UO2; 0.12 apfu) and F (up to 3.81 wt.% F; 0.42 apfu). Strong enrichment of P preferentially involved the berlinite-type substitution (2 Si4+  P5+ + Al3+) implying that significant Al may enter the Si position in zircon. Incorporation of other exotic elements is primarily governed by the xenotime (Si4+ + Zr4+  P5+ + Y3+), pretulite (Sc3+ + P5+  Zr4+ + Si4+), brabantite-type (Ca2+ + (U, Th)4+ + 2P5+  2Zr4+ + 2Si4+), and ximengite-type (Bi3+ + P5+  Zr4+ + Si4+) substitution reactions. One part of the anomalous zircons formed late-magmatically, from a strongly peraluminous, P–F–U-rich hydrous residual melt that gave rise to the zinnwaldite granite. Interaction with aggressive residual fluids and metamictization have further aided in element enrichment or depletion, particularly in altered parts of zircon contained in the protolithionite granite. Most of the zircon from F-rich greisens have a composition close to endmember ZrSiO4 and are chemically distinct from zircon in its granite parent. This discrepancy implies that at Podlesí, granitic zircon became unstable and completely dissolved during greisenization. Part of the mobilized elements was reprecipitated in newly grown, hydrothermal zircon.  相似文献   

14.
2004年7月至2005年6月对三江平原典型湿地系统大气湿沉降中的氮素动态进行了研究,并探讨了其生态效应。结果表明,各形态氮月均浓度之间差别较大,具有明显的季节性,原因主要与人类活动、降水强度及频次、风向、地理位置以及氮氧化物自然排放有关;湿沉降的TN组成以TIN为主(51.38%~98.96%),TIN又以NH4+-N和NO3--N特别是NH4+-N为主,降水天气系统的路径在很大程度上影响着降水中各形态氮的组成;降水量与各形态氮浓度均呈较弱的负相关(p>0.05),而NH4+-N与NO3--N、TON均呈显著正相关(p<0.05),它们可能具有同源性。NH4+-N与NO3--N的良好相关性与其在液相中的反应有关;生长季是全年氮沉降的重要时期,其TN沉降量为非生长季的1.84倍,二者所占比例分别为64.78%和35.22%。除NO2--N外,其它各形态氮的沉降量均以生长季为主体;全年TN沉降量为7.57 kg/hm2,TIN/TON之比为5.47,TIN为沉降主体,占84.56%。NH4+-N和NO3--N是TIN沉降的主体,其所占全年的比例分别为52.55%和30.03%;氮是该区植物生长的限制因素,生长季的氮沉降对于促进植物生长直接生态意义重大,而非生长季的氮沉降对于大量补充次年植物生长初期所需养分的间接生态意义明显,其生态作用不容忽视;近年来湿地系统氮沉降量的降低可能是导致其退化的重要原因,其生态影响也不容忽视。  相似文献   

15.
The cathodoluminescence (CL) of a variety of alkali feldspars from South Greenland has been examined in an attempt to understand the causes of the CL and its petrological significance. Analytical methods have included CL spectroscopy, secondary ion mass spectrometry (SIMS) and electron paramagnetic resonance (EPR) to correlate the presence of certain CL emissions to the presence of certain trace element and point defects. Where possible, blue and red luminescent fractions of the same rock samples have been separated and analysed separately. Blue CL appears to relate to the presence of electron holes on bridging oxygens, particularly on the Al-O-Al bridge, as determined from EPR studies. No correlation with other proposed activators for blue CL such as Eu2+, Ga3+ or Ti4+ was observed. Some blue luminescent feldspars also have an emission in the infra-red (IR), invisible during normal visible CL petrography. The red and IR CL emissions correspond to features in EPR spectra attributed to Fe3+ and support previous suggestions that Fe3+ is related to this emission. However, our studies indicate that the visible red CL relates specifically to Fe3+ on the T1 site, whereas the equivalent CL from disordered feldspars lies in the IR. The difference between red and IR CL emissions therefore relates to the state of Fe3+ order across the tetrahedral sites. These data allow more meaningful interpretations of CL as a petrographic tool in alkali feldspar-bearing rocks. Received: 5 March 1998 / Accepted: 23 November 1998  相似文献   

16.
胶北地块斜长角闪岩的岩石学与年代学研究   总被引：1，自引：0，他引：1       下载免费PDF全文
胶北地块位于华北克拉通东部陆块,胶-辽-吉活动带的南端.胶北地区荆山杂岩中存在一组与高压基性麻粒岩密切共生的斜长角闪岩,是构成前寒武纪变质基底的重要组成部分.岩石学矿物学研究表明,斜长角闪岩记录了3个阶段的变质作用:峰期变质矿物组合（M1）为角闪石1+斜长石+榍石,根据NCKFMASHTO体系的成分视剖面图和角闪石压力计估算出温度条件T=660~715 ℃,压力条件P=0.65~0.71 GPa;其后经历了退变质作用（M2）,矿物组合为角闪石2+绿帘石+斜长石+绿泥石+钠长石,估算温压条件为537~630 ℃/0.41~0.58 GPa;晚期发生前绿片岩相退变质作用（M3）,其矿物组合为钠长石+葡萄石+绿泥石+方解石,其温压条件 < 400 ℃/0.35 GPa.斜长角闪石的CL图像显示其具有较弱的阴极发光效应和弱震荡环带,Th/U比值相对较小（0.06~0.43）,锆石形态和内部结构指示锆石形成于深熔作用过程,21个锆石的LA-ICP-MS定年研究的结果表明,斜长角闪岩记录的最老206Pb/238U年龄为2 075±25 Ma,上交点年龄为1 845±23 Ma（MSWD=0.35）,该组年龄记录了斜长角闪岩峰期变质作用时代的上限.斜长角闪岩在原岩形成以后,可能曾经历麻粒岩相变质作用,并记录了在胶-辽-吉带~1.85 Ga碰撞闭合过程中的深熔事件,此后经历了角闪岩相变质作用,及其二次退变质作用,终结于前绿片岩相的变质温压条件.   相似文献   

17.
Cordierite samples from pegmatites and metamorphic rocks have been analysed for major [electron microprobe analysis (EMPA)] and trace elements [inductively coupled plasma mass spectrometry (ICP-MS), secondary ion mass spectrometry analyses (SIMS)] as well as for H2O and CO2 (coulometric titration), and the results evaluated in conjunction with published data in order to determine which exchange mechanisms are significant. Apart from the homovalent substitutions FeMg−1 and MnMg−1 on the octahedral site, some minor KNa−1 on the Ch0 channel site, and Fe3+Al−1 on the T11 tetrahedral site, the three most important substitution mechanisms are those for the incorporation of Li on the octahedral sites (NaLi□−1Mg−1), and of Be and other divalent cations on the tetrahedral T11 site (NaBe□−1Al−1 and Na(Mg,Fe2+)□−1Al−1). The dominant role of the last vector is clearly demonstrated. We propose a new generalized formula for cordierite: Ch(Na,K)0–1 VI(Mg,Fe2+,Mn,Li)2 IVSi5 IVAl3 IV(Al, Be, Mg, Fe2+, Fe3+)O18 *xCh(H2O, CO2…). Our results show that the population of (Mg, Fe2+) on the T11-site is limited to about 0.08 a.p.f.u. Other exchange mechanisms that were encountered in experiments operate only under P–T conditions or in bulk compositions that are rarely realized in nature. Routine analyses by electron microprobe in which Li and Be are not determined can be plotted as (Mg+Fe+Mn) versus (Si+Al) to assess whether significant amounts of Li and Be could be present. These amounts can be calculated as Li (a.p.f.u.)=Al+Na–4 and Be (a.p.f.u.)=10–2Al–M2+–Na.  相似文献   

18.
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+.  相似文献   

19.
J.-R. Disnar  J. Trichet   《Chemical Geology》1983,40(3-4):203-223
The thermal decomposition of complexes formed by reactions of various divalent cations (UO22+, Cu2+, Pb2+, Ni2+, Mn2+, Zn2+ and Co2+) with a Recent sedimentary organic matter of algal origin has been studied by thermogravimetric analyses carried out under an inert atmosphere. Results of these experiments show that metals fixed by the organic matter delay the beginning of the decomposition of that latter one. The importance of this retardating effect depends on: (1) the nature of the metal (Mn > Pb > Ni > Co > Zn > U > Cu > pure organic matter); and, to a lesser degree, (2) its content in the tested complex.

Chromatographic analyses of gases (H2O, CO2, light hydrocarbons) produced during the experiments show that carbon dioxide is the main decomposition product of the complexes. As a matter of fact, carbon dioxide is formed all along the thermal decomposition of the organic matter. For the uranium-containing complex, a sudden emission of CO2 may be related to the reduction of this metal which passes from oxidation state VI to IV during the pyrolysis.

These observations support the hypothesis that metals associated with sedimentary organic complexes may affect their diagenetic evolution.

Résumé

La décomposition thermique de composés formés par réaction de différents cations divalents (UO2+2, Cu2+, Pb2+, Ni2+, Mn2+, Zn2+, Co2+) avec une matière sédimentaire actuelle d'origine algaire a été suivie par analyse thermogravimétrique, en opérant à atmosphère inerte. les résultats de ces expériences montrent que les métaux associés à la matière organique retardent le début de la décomposition de celle-ci. Cet effect retardateur dépend: (1) de la nature du métal étudié (Mn > Pb > Ni > Co > Zn > U > Cu); et dans une moindre mesure, (2) de la teneur de celui-ci dans le produit considéré.

L'analyse chromatographique des principaux composés gazeux (CO2, H2O, hydrocarbures légers) émis durant les expériences, montre que l'anhydride carbonique est un produit majeur de la décomposition des échantillons étudiés. En effet, contrairement aux autres composés analysés, le CO2 est émis durant toute la durée de la pyrolyse de la matière organique. Les courbes d'émission du CO2 obtenues à partir des complexes contenant de l'U montrent un dégagement soudain de CO2 qui est peut-être à relier à la réduction du métal qui passe de l'état d'oxydation VI à IV au cours de la pyrolyse.

Ces observations appuient l'hypothèse selon laquelle des métaux associés à des matériaux organiques sédimentaires pourraient influer sur les transformations subies par ceux-ci au cours de leur évolution diagénétique.  相似文献   


20.
定量评价硫酸对岩溶碳汇效应的影响有助于提高岩石风化碳汇通量估算精度, 对当前全球气候变化研究意义重大.选取受酸雨影响的桂林岩溶区为研究对象, 在枯水期对研究区14个岩溶大泉和15条地下河水化学成分和碳同位素进行了测试分析, 结果表明: 岩溶大泉和地下河中阳离子以Mg2+和Ca2+为主, 阴离子以HCO3-为主, 分别占阳离子和阴离子组成的90%以上, SO42-含量较低, 其含量范围为0.004~0.213mmol/L; 所占阴离子组成比例为0.12%~6.11%;δ13CDIC、[Ca2++Mg2+]/[HCO3-]更偏向于碳酸溶解端元, 离硫酸溶解端元距离远, 证实硫酸参与碳酸盐岩的溶解对地下水无机碳(dissolved inorganic carbon, 简称DIC)及δ13CDIC的影响有限; 与Sr2+/Ca2+值一样, δ13CDIC主要受径流条件控制, 其大小可以反映地下水径流条件的强弱.利用化学计量关系计算出由硫酸溶蚀碳酸盐岩的平均比例为22.64%, 产生的DIC(HCO3-H2SO4)占总DIC的平均比例为13.04%, 碳酸产生的DIC(HCO3-H2CO3)占地下水总DIC的比例为86.96%, 其中来源于土壤大气中的HCO3-比例为43.48%.因此, 扣除硫酸对地下水中DIC的贡献后, 岩溶碳汇效应将减少13.04%.   相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号