Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-8029
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMaslyk, Marcel-
dc.contributor.authorGäb, Tobias-
dc.contributor.authorMatveeva, Galina-
dc.contributor.authorOpitz, Phil-
dc.contributor.authorMondeshki, Mihail-
dc.contributor.authorKrysiak, Yasar-
dc.contributor.authorKolb, Ute-
dc.contributor.authorTremel, Wolfgang-
dc.date.accessioned2022-10-25T09:10:47Z-
dc.date.available2022-10-25T09:10:47Z-
dc.date.issued2022-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8044-
dc.description.abstractConcrete is the most prevalent manufactured material that has shaped the built environment, but the high-temperature production of cement, the main component of concrete, has a massive carbon footprint. It is shown that CO2 emissions during clinker production of cement can be circumvented by a metathesis reaction at room temperature in ball-mills, where the cement clinker is replaced by non-calcined limestone and alkali-activated binders/geopolymers. An amorphous intermediate (aNaSiCC) containing a random mixture of the ionic constituents in “molecular” dispersion is formed by mechanochemical activation of CaCO3 and Na2SiO3. This allows molecular transport during crystallization and low activated reactions, as precipitation of solids from liquids (nucleation limited and kinetically controlled) and solid-state transformations (diffusion-limited and thermodynamically controlled) have equal weight. Several steps of the hydration reaction could be resolved. Activating the amorphous aNaSiCC precursor with NaOH leads to a CSH-like phase with a C/S ratio of ≈1 containing some sodium. The carbonate components pass through a multistep crystallization from aNaSiCC via pirssonite and gaylussite to monohydrocalcite. The findings help unravel the interplay between thermodynamics and kinetics in complex reactions of alkali-activated binders and for CaCO3 crystallization in industrial and geochemical settings, where dissolved silicate is always involved.en_GB
dc.language.isoengde
dc.rightsCC BY-NC-ND*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleMultistep crystallization pathways in the ambient-temperature synthesis of a new alkali-activated binderen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-8029-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleAdvanced functional materialsde
jgu.journal.volume32de
jgu.journal.issue7de
jgu.pages.alternative2108126de
jgu.publisher.year2022-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.issn1616-3028de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/adfm.202108126de
jgu.organisation.rorhttps://ror.org/023b0x485-
Appears in collections:JGU-Publikationen

Files in This Item:
  File Description SizeFormat
Thumbnail
multistep_crystallization_pat-20221025111127196.pdf1.78 MBAdobe PDFView/Open