Chapter 26- Metamorphic Reactions.ppt

1、Chapter 26: Metamorphic Reactions,If we treat isograds as reactions, we can: Understand what physical variables might affect the location of a particular isograd We may also be able to estimate the P-T-X conditions that an isograd represents,From Understanding Earth, Press and Siever. Freeman.,1. Ph

2、ase Transformations,Isochemical Polymorphs of SiO2 or Al2SiO5 or graphite-diamond or calcite-aragonite Simplest: depend on temperature and pressure only,1. Phase Transformations,Figure 26.1. A portion of the equilibrium boundary for the calcite-aragonite phase transformation in the CaCO3 system. Aft

3、er Johannes and Puhan (1971), Contrib. Mineral. Petrol., 31, 28-38. Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,1. Phase Transformations,Figure 26.15. The P-T phase diagram for the system Al2SiO5 showing the stability fields for the three polymorphs andalusite,

4、 kyanite, and sillimanite. Calculated using the program TWQ (Berman, 1988, 1990, 1991). Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,1. Phase Transformations,Small DS for most polymorphic transformations small DG between two alternative polymorphs, even several

5、tens of degrees from the equilibrium boundary little driving force for the reaction to proceed common metastable relics in the stability field of other Coexisting polymorphs may therefore represent non-equilibrium states (overstepped equilibrium curves or polymetamorphic overprints),2. Exsolution,Fi

6、gure 6.16. T-X phase diagram of the system albite-orthoclase at 0.2 GPa H2O pressure. After Bowen and Tuttle (1950). J. Geology, 58, 489-511. Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,3. Solid-Solid Net-Transfer Reactions,Involve solids only Differ from polym

7、orphic transformations: involve solids of differing composition, and thus material must diffuse from one site to another for the reaction to proceed,3. Solid-Solid Net-Transfer Reactions,Examples:NaAlSi2O6 + SiO2 = NaAlSi3O8 Jd Qtz AbMgSiO3 + CaAl2Si2O8 = CaMgSi2O6 + Al2SiO5 En An Di And4 (Mg,Fe)SiO

8、3 + CaAl2Si2O8 = Opx Plag (Mg,Fe)3Al2Si3O12 + Ca(Mg,Fe)Si2O6 + SiO2 Gnt Cpx Qtz,Figure 27-1. Temperature-pressure phase diagram for the reaction: Albite = Jadeite + Quartz calculated using the program TWQ of Berman (1988, 1990, 1991). Winter (2010) An Introduction to Igneous and Metamorphic Petrolog

9、y. Prentice Hall.,3. Solid-Solid Net-Transfer Reactions,If minerals contain volatiles, the volatiles must be conserved in the reaction so that no fluid phase is generated or consumed For example, the reaction: Mg3Si4O10(OH)2 + 4 MgSiO3 = Mg7Si8O22(OH)2 Tlc En Ath involves hydrous phases, but conserv

10、es H2O It may therefore be treated as a solid-solid net-transfer reaction,3. Solid-Solid Net-Transfer Reactions,When solid-solution is limited, solid-solid net-transfer reactions are discontinuous reactions Discontinuous reactions tend to run to completion at a single temperature (at a particular pr

11、essure) There is thus an abrupt (discontinuous) change from the reactant assemblage to the product assemblage at the reaction isograd,4. Devolatilization Reactions,Among the most common metamorphic reactions H2O-CO2 systems are most common, but the principles same for any reaction involving volatile

12、s Reactions dependent not only upon temperature and pressure, but also upon the partial pressure of the volatile species,4. Devolatilization Reactions,For example the location on a P-T phase diagram of the dehydration reaction:KAl2Si3AlO10(OH)2 + SiO2 = KAlSi3O8 + Al2SiO5 + H2O Ms Qtz Kfs Sill Wdepe

13、nds upon the partial pressure of H2O (pH2O) This dependence is easily demonstrated by applying Le Chteliers principle to the reaction at equilibrium,4. Devolatilization Reactions,The equilibrium curve represents equilibrium between the reactants and products under water-saturated conditions (pH2O =

14、PLithostatic),Figure 26.2(a). P-T phase diagram for the reaction Ms + Qtz = Kfs + Al2SiO5 + H2O showing the shift in equilibrium conditions as pH2O varies (assuming ideal H2O-CO2 mixing). Calculated using the program TWQ by Berman (1988, 1990, 1991). After Winter (2010) An Introduction to Igneous an

15、d Metamorphic Petrology. Prentice Hall.,KAl2Si3AlO10(OH)2 + SiO2 = KAlSi3O8 + Al2SiO5 + H2O Ms Qtz Kfs Sill W,Suppose H2O is withdrawn from the system at some point on the water-saturated equilibrium curve: pH2O Plithostatic According to Le Chteliers Principle, removing water at equilibrium will be

16、compensated by the reaction running to the right, thereby producing more water This has the effect of stabilizing the right side of the reaction at the expense of the left side So as water is withdrawn the Kfs + Sill + H2O field expands slightly at the expense of the Mu + Qtz field, and the reaction

17、 curve shifts toward lower temperature,Figure 26.2. P-T phase diagram for the reaction Ms + Qtz = Kfs + Al2SiO5 + H2O showing the shift in equilibrium conditions as pH2O varies (assuming ideal H2O-CO2 mixing). Calculated using the program TWQ by Berman (1988, 1990, 1991). Winter (2010) An Introducti

18、on to Igneous and Metamorphic Petrology. Prentice Hall.,4. Devolatilization Reactions,pH2O can become less than PLith by either of two ways Pfluid PLith by drying out the rock and reducing the fluid content Pfluid = PLith, but the water in the fluid can become diluted by adding another fluid compone

19、nt, such as CO2 or some other volatile phase In Fig. 26.2 I calculated the curves for the latter case on the basis of ideal H2O-CO2 mixing,4. Devolatilization Reactions,An important point arising from Fig. 26.2 is:The temperature of an isograd based on a devolatilization reaction is sensitive to the

20、 partial pressure of the volatile species involved An alternative: T-Xfluid phase diagram Because H2O and CO2 are by far the most common metamorphic volatiles, the X in T-X diagrams is usually the mole fraction of CO2 (or H2O) in H2O-CO2 mixtures Because pressure is also a common variable, a TXfluid

21、 diagram must be created for a specified pressure,4. Devolatilization Reactions,Figure 26.4. T-XH2O phase diagram for the reaction Ms + Qtz = Kfs + Sil + H2O at 0.5 GPa assuming ideal H2O-CO2 mixing, calculated using the program TWQ by Berman (1988, 1990, 1991). Winter (2010) An Introduction to Igne

22、ous and Metamorphic Petrology. Prentice Hall.,4. Devolatilization Reactions,Figure 26.4. Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,Figure 26.2. Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,4. Devolatilization Reactions,Sh

23、ape of all dehydration curves on T-Xfluid diagrams is similar to the curve in Fig. 26.2 Maximum temperature at the pure H2O end, and slope gently at high XH2O, but steeper toward low XH2O, becoming near vertical at very low XH2O Reaction temperature can thus be practically any temperature below the

24、maximum at pH2O = Plith Must constrain the fluid composition (if possible) before using a dehydration reaction to indicate metamorphic grade,Figure 26.3. Calculated P-T equilibrium reaction curve for a dehydration reaction illustrating the full loop that is theoretically possible. From Winter (2010)

25、. An Introduction to Igneous and Metamorphic Petrology, Prentice Hall.,A rare exception,4. Devolatilization Reactions,Decarbonation reactions may be treated in an identical fashion For example, the reaction: CaCO3 + SiO2 = CaSiO3 + CO2 (26.6)Cal Qtz Wo Can also be shown on a T-XCO2 diagram Has the s

26、ame form as reaction (26.5), only the maximum thermal stability of the carbonate mineral assemblage occurs at pure XCO2,4. Devolatilization Reactions,P-T phase diagram for the reaction Cal + Qtz = Wo + CO2,Figure 26.5. T-XCO2 phase diagram for the reaction Cal + Qtz = Wo + CO2 at 0.5 GPa assuming id

27、eal H2O-CO2 mixing, calculated using the program TWQ by Berman (1988, 1990, 1991). Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,5 types of devolatilization reactions, each with a unique general shape on a T-X diagram Type 3: Tmax at XCO2 determined by the stoich

28、iometric ratio of CO2/H2O produced,Ca2Mg5Si8O22(OH)2 + 3 CaCO3 + 2 SiO2 Tr Cal Qtz = 5 CaMgSi2O6 + 3 CO2 + H2O Di,Figure 26.6. Schematic T-XCO2 phase diagram illustrating the general shapes of the five types of reactions involving CO2 and H2O fluids. After Greenwood (1967). In P. H. Abelson (ed.), R

29、esearches in Geochemistry. John Wiley. New York. V. 2, 542-567. Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,5. Continuous Reactions,Figure 26.8. Geologic map of a hypothetical field area in which metamorphosed pelitic sediments strike directly up metamorphic gr

30、ade. From Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,5. Continuous Reactions,Two possible reasons: 1. Such contrasting composition that the garnet reaction is differentExample: garnet in some pelites may be created by the (unbalanced) reaction:Chl + Ms + Qtz G

31、rt + Bt + H2O (26.11)Whereas in more Fe-rich and K-poor pelites, garnet might be generated by an (unbalanced) reaction involving chloritoid:Chl + Cld + Qtz Grt + H2O (26.12),5. Continuous Reactions,2. The reaction on which the isograd is based is the same in each unit, but it is a continuous reactio

32、n, and its location is sensitive to the composition of the solutions (either solid of fluid) involvedThe offsets this creates in an isograd are usually more subtle than for reason #1, but in some cases they can be substantialWe will concentrate on this second reason here,5. Continuous Reactions,Fig.

33、 6.10. Isobaric T-X phase diagram at atmospheric pressure After Bowen and Shairer (1932), Amer. J. Sci. 5th Ser., 24, 177-213. Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,“Melt-in” isograd?,5. Continuous Reactions,Discontinuous reactions occur at a constant gra

34、deChl + Ms + Qtz Grt + Bt + H2O (26.11) in KFASH F = C f + 2 = 5 4 + 2 = 1,5. Continuous Reactions,If Chl + Ms + Qtz Grt + Bt + H2O (26.11) in KFMASHwere a continuous reaction, then we would find chlorite, muscovite, quartz, biotite, and garnet all together in the same rock over an interval of metam

35、orphic grade above the garnet-in isograd The composition of solid solution phases vary across the interval, and the proportions of the minerals changes until one of the reactants disappears with increasing grade,Continuous reactions occur when F 1, and the reactants and products coexist over a tempe

36、rature (or grade) interval,Fig. 26.9a. Schematic isobaric T-XMg diagram representing the simplified metamorphic reaction Chl + Qtz Grt + H2O. From Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,Pseudosections address (only) the reactions (continuous or discontinuo

37、us) affecting a rock of specific Xbulk,Fig. 26.9b. Schematic P-T “pseudosection” for a specific bulk composition (in this case for Mg/(Mg + Fe) = 0.5 and quartz-excess) showing the stability fields of Chl + Qtz, Chl + Grt + Qtz, and Grt + Qtz. Note the continuous nature of the reaction when all soli

38、d phases are present (shaded area). Note also that one can contour the shaded divariant field in (b) for specific compositions of either garnet (as has been done) or chlorite. The boundaries and contours would change for a different Xbulk (i.e. different XMg), and even the field assemblages might ch

39、ange: for example the higher temperature garnet + quartz field would be garnet + chlorite if the SiO2 content were so low that quartz were consumed before chlorite by the reaction. From Winter (2010) An Introduction to Igneous and Metamorphic Petrology.,6. Ion Exchange Reactions,Reciprocal exchange

40、of components between 2 or more minerals MgSiO3 + CaFeSi2O6 = FeSiO3 + CaMgSi2O6 Annite + Pyrope = Phlogopite + Almandine Expressed as pure end-members, but really involves Mg-Fe (or other) exchange between intermediate solutions Basis for many geothermobarometers Causes rotation of tie-lines on com

41、patibility diagrams,Figure 27.6. AFM projections showing the relative distribution of Fe and Mg in garnet vs. biotite at approximately 500oC (a) and 800oC (b). From Spear (1993) Metamorphic Phase Equilibria and Pressure-Temperature-Time Paths. Mineral. Soc. Amer. Monograph 1. MSA. Winter (2010) An I

42、ntroduction to Igneous and Metamorphic Petrology. Prentice Hall.,6. Redox Reactions,Involves a change in oxidation state of an element 6 Fe2O3 = 4 Fe3O4 + O2 2 Fe3O4 + 3 SiO2 = 3 Fe2SiO4 + O2,At any particular pressure these become oxygen buffers,Fig. 26.10. Isobaric T-fO2 diagram showing the locati

43、on of reactions (26.13) - (26.15) used to buffer oxygen in experimental systems. After Frost (1991), Rev. in Mineralogy, 25, MSA, pp. 469-488. Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,7. Reactions Involving Dissolved Species,Minerals plus ions neutral molecu

44、les dissolved in a fluid One example is hydrolysis: 2 KAlSi3O8 + 2 H+ + H2O = Al2Si2O5 (OH)4 + SiO2 + 2 K+Kfs aq. species kaolinite aq. species,Can treat such reactions in terms of the phase rule and the intensive variables: P, T, and concentrations of the reactant species T-P diagrams for fixed or

45、contoured Ci Isobaric T-Ci diagrams Isobaric and isothermal Ci - Cj diagrams Reaction above might be handled by a T vs. CK+/CH+ diagram,Reactions and Chemographics,We can use chemographics to infer reactions,Any two phases in a binary system can react to from a phase between them,Fo + Qtz = En Mg2Si

46、O4 + SiO2 = Mg2Si2O6 En + Per = Fo Mg2Si2O6 + 2 MgO = 2 Mg2SiO4 Per + Qtz = Fo or En If we know the chemographics we can determine that a reaction is possible (and can dispense with balancing it),Reactions and Chemographics,What reaction does this ternary system allow?,Fig. 26.12. From Winter (2010)

47、 An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,Reactions and Chemographics,A + B + C = X,below x-in isograd,above x-in isograd,Reactions and Chemographics,What reaction does this system allow?,Fig. 26.13. From Winter (2010) An Introduction to Igneous and Metamorphic Petrology.

48、 Prentice Hall.,Reactions and Chemographics,What reaction is possible between A-B-C-D?,Fig. 26.14a. From Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,A compatibility diagram for some metamorphic zone,A + B = C + D,This is called a tie-line flip, and results in n

49、ew groupings in the next metamorphic zone,At the isograd,Above the isograd,Below the isograd,Fig. 26.14. From Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,Petrogenetic Grids,P-T diagrams for multicomponent systems that show a set of reactions, generally for a sp

50、ecific rock type,Petrogenetic grid for mafic rocks,Fig. 26.19. Simplified petrogenetic grid for metamorphosed mafic rocks showing the location of several determined univariant reactions in the CaO-MgO-Al2O3-SiO2-H2O-(Na2O) system (“C(N)MASH”). Winter (2010) An Introduction to Igneous and Metamorphic Petrology. Prentice Hall.,