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Neuhoff, P. S., Bird, D. K. (2001) Partial dehydration of laumontite: thermodynamic constraints and petrogenetic implications. Mineralogical Magazine, 65 (1) 59-70 doi:10.1180/002646101550127

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Reference TypeJournal (article/letter/editorial)
TitlePartial dehydration of laumontite: thermodynamic constraints and petrogenetic implications
JournalMineralogical Magazine
AuthorsNeuhoff, P. S.Author
Bird, D. K.Author
Year2001 (February)Volume65
Page(s)59-70Issue1
PublisherMineralogical Society
DOIdoi:10.1180/002646101550127Search in ResearchGate
Mindat Ref. ID243250Long-form Identifiermindat:1:5:243250:6
GUID08137be0-3a91-424a-b85e-29d80176fb64
Full ReferenceNeuhoff, P. S., Bird, D. K. (2001) Partial dehydration of laumontite: thermodynamic constraints and petrogenetic implications. Mineralogical Magazine, 65 (1) 59-70 doi:10.1180/002646101550127
Plain TextNeuhoff, P. S., Bird, D. K. (2001) Partial dehydration of laumontite: thermodynamic constraints and petrogenetic implications. Mineralogical Magazine, 65 (1) 59-70 doi:10.1180/002646101550127
Abstract/NotesAbstractLaumontite is a common zeolite mineral indicative of low-grade metamorphism of lavas and volcaniclastic sediments. Stoichiometric laumontite (CaAl2Si4O12·4.5H2O) dehydrates in air at 298.15 K, 1 bar to leonhardite (CaAl2Si4O12·3.5H2O) via loss of water from the W1 crystallographic site. Consideration of reported X-ray diffraction and calorimetric data indicates that the standard molal volume and entropy for dehydration of laumontite to leonhardite + liquid water are ∼13 cc/mol and ∼8 cal/molK, respectively, at 298.15 K, 1 bar. Equilibrium between laumontite and leonhardite occurs at 70 to 80% relative humidity at 298.15 K, 1 bar, corresponding to a standard molal Gibbs energy and enthalpy of reaction of ∼170±40 and ∼2630±100 cal/mol, respectively. Calculated univariant equilibrium for this reaction is nearly linear from 46±3°C at 1 bar to 235±3°C at 5000 bar. Comparison of geological observations with these results suggests that laumontite forms as ‘leonhardite’ during metamorphism and diagenesis. Consideration of ‘leonhardite’, instead of laumontite, in low-grade metamorphic phase relations facilitates prediction of the relative stabilities of zeolites in natural and geologic systems, where calculated entropies of reaction incorrectly predict that assemblages bearing fully hydrated laumontite are stable at lower temperatures than the zeolites heulandite and stilbite.


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