基于热重分析的菱镁矿分解动力学解析

本文利用热重(TG)分析方法,探讨了菱镁矿的热分解过程。根据热微商(DTG)曲线峰顶温度,结合Kissinger及Ozawa-Doyle方法拟合计算得到菱镁矿热分解的活化能和指前因子(lgA)分别为211.55 kJ/mol和11.07s-1。依次采用单曲线拟合、多元非线性拟合及Malek方法判定得出菱镁矿热分解过程属于三维相界反应模型(R3),其动力学方程为:dα/d T=(1011.07/β)·e-211.55×103/(8.314×T)·3(1-α)2/3。     

Thermonuclear reaction rates from (p,n) reactions on targets withA = 92–122

From the experimentally measured (p,n) cross-sections for^92,94Zr,⁹³Nb,^95,96,98Mo,¹⁰³Rh,^107,109Ag,¹¹⁰Pd,¹¹⁵In,^117,122Sn nuclides, for proton energies below 7 MeV, thermonuclear reaction rates in the temperature range 1≤T ₉≤5(T₉=10⁹ K) have been extracted. These reaction rates have been fitted to a three parameter empirical expression proposed by Fowler.     

Meso‐scale particle modeling of concrete deterioration caused by alkali‐aggregate reaction

A meso‐scale particle model is presented to simulate the expansion of concrete subjected to alkali‐aggregate reaction (AAR) and to analyze the AAR‐induced degradation of the mechanical properties. It is the first attempt to evaluate the deterioration mechanism due to AAR using the discrete‐element method. A three‐phase meso‐scale model for concrete composed of aggregates, mortar and the interface is established with the combination of a pre‐processing approach and the particle flow code, PFC2D. A homogeneous aggregate expansion approach is applied to model the AAR expansion. Uniaxial compression tests are conducted for the AAR‐affected concrete to examine the effects on the mechanical properties. Two specimens with different aggregate sizes are analyzed to consider the effects of aggregate size on AAR. The results show that the meso‐scale particle model is valid to predict the expansion and the internal micro‐cracking patterns caused by AAR. The two different specimens exhibit similar behavior. The Young's modulus and compressive strength are significantly reduced with the increase of AAR expansion. The shape of the stress–strain curves obtained from the compression tests clearly reflects the influence of internal micro‐cracks: an increased nonlinearity before the peak loading and a more gradual softening for more severely affected specimens. Similar macroscopic failure patterns of the specimens under compression are observed in terms of diagonal macroscopic cracks splitting the specimen into several triangular pieces, whereas localized micro‐cracks forming in slightly affected specimens are different from branching and diffusing cracks in severely affected ones, demonstrating different failure mechanisms. Copyright © 2012 John Wiley & Sons, Ltd.     

强磁场对中子星壳层热核反应的影响

本文通过考虑强磁场中电子的量子效应，分析了强磁场下电子气体的Fermi能，讨论了磁场对核的屏蔽势和核反应率的影响，进而计算了强磁场对天体物理中几个较重要的热核反应的影响，结果表明，相对于无磁场而言，在较低密度下，足够强的磁场使原子核的屏蔽势显著增加，但在ρ／μe＞10~5molcm~(-3)的密度下，中子星表面存在的强度为10~5～10~9T范围内的磁场对核反应率几乎没有影响。     

Isograds and P–T evolution in the eastern Lepontine Alps (Graubünden, Switzerland)

Reactions producing Al‐rich index minerals in the south‐eastern part of the Lepontine Dome (Central Alps, Switzerland) are investigated using mineral distribution maps, microstructural observations and equilibrium phase diagrams. The apparent staurolite mineral zone boundary corresponds to the paragonite breakdown reaction Pg + Grt + Qtz = Pl + Al₂O₃ + W. Equilibrium phase diagrams show that most natural metapelites do not contain staurolite or alumosilicates as long as univalent cations are predominantly accommodated in white mica. For a wide range of metapelitic compositions the paragonite breakdown releases sufficient Al for the formation of these minerals. Rare occurrences of staurolite and kyanite, north of the formerly mapped mineral zone boundaries, coexist with paragonite and are restricted to extremely Al‐rich bulk compositions. The stable branch of the kyanite‐forming paragonite breakdown reaction above 660 °C yields an additional mapable isograd. The second set of Al‐releasing reactions is biotite‐producing phengite breakdown. However, these reactions are less suitable to produce well defined reaction isograds in the field as they are more continuous and their progress is strongly dependent on bulk composition. Well developed fibrolite in metapelites does not appear until staurolite starts to breakdown. We conclude that amphibolite facies conditions in the study area were attained by decompression, without substantial heating at low pressures.     

江陵凹陷新生代玄武岩水-岩反应模拟及其对富钾卤水成因的指示

关于江陵凹陷富钾卤水的物质来源和成因机理仍未查明. 对凹陷新生代玄武岩开展矿物学、岩石学、地球化学研究以及水-岩反应模拟实验,重点研究时间、温度、流体成分等对水-岩反应的影响. 结果表明,卤水具有高锂低镁的特征,说明其在成因上受到火山活动的影响;研究区岩浆发生不同程度的分异,玄武岩蚀变作用强烈,表明地下热液的交代作用强烈,玄武岩通过水-岩反应为富钾卤水矿提供了物质来源;温度是流体对元素的淋滤能力的主要控制因素,高盐度流体是各成矿元素主要的迁移载体,水-岩反应是卤水形成的重要过程.      

High pressure metamorphism in the nappes of the Valle dell'Orco traverse (Western Alps collisional belt) *

Abstract A detailed field and petrological study of rocks from nappes cut by the Valle dell'Orco (Italian Western Alps), in particular the Sesia–Lanzo composite unit, has revealed geological and metamorphic histories which started in pre-alpine times and lasted up to the alpine subduction-collisional processes. During these processes the nappes sustained an early high P–low T stage and a later low P greenschist facies stage, but followed partly distinctive P–T–time trajectories. This paper discusses the kinematic evolution and the thermal history of the alpine belt from the early subduction/underthrust to the later exhumation stage. The metamorphic crystallization is often governed by incomplete and/or local equilibrium, and the pervasive syn-metamorphic deformation and the composition of the syn-metamorphic fluid phase (if present) have exerted an effective local control on reaction kinetics.     

Progressive metamorphism in a crustal-scale shear zone: an example from the Léon region, north-west Brittany, France

This paper describes the progressive metamorphism and deformation of a series of metasediments, Le Conquet Schists and their higher grade equivalents, which occur as tectonically emplaced screens within a sequence of foliated gneisses, the Gneiss de Brest and Gneiss de Lesneven. The sequence exhibits a steep south to north increase in metamorphic grade from garnet-staurolite schist to sillimanite gneiss and sillimanite-K-feldspar migmatite. The relationship of mineral growth to foliation development has been established for individual screens. At least five phases of deformation (D1-D5) are preserved. Analysis of porphyroblast inclusion trails is used to demonstrate sequential mineral growth during the successive development of orthogonal foliations S1-S4. Porphyroblasts continued to grow during the subsequent development of C-S mylonite fabrics and extensional crenulation cleavages which are genetically related to a series of high-strain zones (D5). Mineral assemblages, phase relations and mineral chemistry are consistent with porphyroblast growth being the result of continuous reactions. Microstructure-porphyroblast relations are used to show that although mineral growth proceeded during continuous reactions, these only operated episodically. Phase relations, mineral chemistry and P-T estimates are used to constrain P-T trajectories and these are linked to the deformation histories within individual screens. A comparison between the resulting pressure-temperature-deformation paths is used to demonstrate that the metamorphic peak occurred progressively later and at successively lower pressures with increasing metamorphic grade. It is suggested that the early evolution of the belt is the result of crustal thickening by overthrusting. The subsequent history is one of progressive heating and unroofing of the higher grade rocks in a dextral strike-slip transtensional shear zone.     

Continuous reactions with amphibole, garnet and plagioclase

Abstract End-member, continuous and degenerate reactions are derived for the multisystem with the six components Na₂O, CaO, (Mg/Fe)O, Al₂O₃, SiO₂, H₂O among the phases plagioclase_ss, garnet_ss, amphibole_ss, cpx, opx, olivine, spinel, quartz and an aqueous fluid. The chemography of this system is degenerate due to the co-linearity 2Opx = Ol + Qtz. This co-linearity has its implications both on reaction space and phase equilibria. From a total of 28 reaction systems, reaction space is derived for nine subsystems (phases in parentheses are absent): Case A₁: (Cpx,Ol) (Cpx,Opx) and (Cpx,Qtz), Case A₂: (Spl,Ol) (Spl,Opx) and (Spl,Qtz), Case B: (Ol,Opx) (Ol,Qtz) and (Opx,Qtz). In the absence of either cpx or spl (case A), three reactions form an invariant point, either [Cpx] or [Spl], where the co-linear phases olivine, opx and quartz coexist on the transformation line 2Opx = Ol + Qtz. Changing mineral compositions force invariant points to move along the line with the different reaction curves changing their relative position according to Schreinemakers’rules. Zero contours, i.e. the location where (a) phase(s) disappear(s) in reaction space correspond to singular points in phase diagrams. Two types are distinguished; singular points of indispensable and of substitutable phases. In the first case the phase disappears from the entire bundle while in the second it disappears from a single reaction. In the specific case where the substitutable phases are also the co-linear ones, two of the three co-linear phases disappear simultaneously. Two of the three reaction curves coincide. In the system including Cpx and Spl (Case B) three reactions, (Ol,Opx) (Ol,Qtz) and (Opx,Qtz), oppose three invariant points, [Ol], [Opx] and [Qtz]. Invariant points no longer move along the line 2Opx = Ol + Qtz. The coincidence of the zero contours of all three co-linear phases in reaction space-the result of the chemographic degeneracy-causes the respective singular points to coincide in the phase diagrams. This is the location where curves must be rearranged in a bundle to conform Schreinemakers’rules. The reaction Grs₁Prp₂= 2 Ol + An is fourth order degenerate and part of all nine subsystems (cases A and B). It can be used to relate the different phase diagrams to one another.     

A New Interpretation of Centimetre-scale Variations in the Progress of Infiltration-driven Metamorphic Reactions: Case Study of Carbonated Metaperidotite, Val d'Efra, Central Alps, Switzerland

Progress () of the infiltration-driven reaction, 4olivine +5CO₂ + H₂O = talc + 5magnesite, that occurred during Barrovianregional metamorphism, varies at the cm-scale by a factor of3·5 within an 3 m³ volume of rock. Mineral and stableisotope compositions record that X_CO2, ¹⁸O_fluid, and ¹³C_fluidwere uniform within error of measurement in the same rock volume.The conventional interpretation of small-scale variations in in terms of channelized fluid flow cannot explain the uniformityin fluid composition. Small-scale variations in resulted insteadbecause (a) reactant olivine was a solid solution, (b) initiallythere were small-scale variations in the amount and compositionof olivine, and (c) fluid composition was completely homogenizedover the same scale by diffusion–dispersion during infiltrationand subsequent reaction. Assuming isochemical reaction, spatialvariations in image variations in the (Mg + Fe)/Si of the parentrock rather than the geometry of metamorphic fluid flow. Ifinfiltration-driven reactions involve minerals fixed in composition,on the other hand, spatial variations in do directly imagefluid flow paths. The geometry of fluid flow can never be determinedfrom geochemical tracers over a distance smaller than the oneover which fluid composition is completely homogenized by diffusion–dispersion. KEY WORDS: Alpine Barrovian metamorphism; diffusion; metamorphic fluid composition; metamorphic fluid flow; reaction progress