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Influences of Dilute Organic Adsorbates on the Hydration of Low-Surface-Area Silicates
- Source :
- Journal of the American Chemical Society, Journal of the American Chemical Society, American Chemical Society, 2015, 137 (25), pp.8096-8112. ⟨10.1021/jacs.5b00622⟩, Journal of the American Chemical Society, 2015, 137 (25), pp.8096-8112. ⟨10.1021/jacs.5b00622⟩
- Publisher :
- American Chemical Society
-
Abstract
- International audience; Competitive adsorption of dilute quantities of certain organic molecules and water at silicate surfaces strongly influence the rates of silicate dissolution, hydration, and crystallization. Here, we determine the molecular-level structures, compositions, and site-specific interactions of adsorbed organic molecules at low absolute bulk concentrations on heterogeneous silicate particle surfaces at early stages of hydration. Specifically, dilute quantities (similar to 0.1% by weight of solids) of the disaccharide sucrose or industrially important phosphonic acid species slow dramatically the hydration of low-surface-area (similar to 1 m(2)/g) silicate particles. Here, the physicochemically distinct adsorption interactions of these organic species are established by using dynamic nuclear polarization (DNP) surface-enhanced solid-state NMR techniques. These measurements provide significantly improved signal sensitivity for near-surface species that is crucial for the detection and analysis of dilute adsorbed organic molecules and silicate species on low-surface-area particles, which until now have been infeasible to characterize. DNP-enhanced 2D Si-29{H-1}, C-13{H-1}, and P-31{H-1} heteronuclear correlation and 1D Si-29{C-13} rotational-echo double-resonance NMR measurements establish hydrogen-bond-mediated adsorption of sucrose at distinct nonhydrated and hydrated silicate surface sites and electrostatic interactions with surface Ca2+ cations. By comparison, phosphonic acid molecules are found to adsorb electrostatically at or near cationic calcium surface sites to form Ca(2+)phosphonate complexes. Although dilute quantities of both types of organic molecules effectively inhibit hydration, they do so by adsorbing in distinct ways that depend on their specific architectures and physicochemical interactions. The results demonstrate the feasibility of using DNP-enhanced NMR techniques to measure and assess dilute adsorbed molecules and their molecular interactions on low-surface-area materials, notably for compositions that are industrially relevant.
- Subjects :
- IONS
Sucrose
C-13
Cations, Divalent
Surface Properties
Inorganic chemistry
TRICALCIUM SILICATE
02 engineering and technology
010402 general chemistry
01 natural sciences
Biochemistry
Catalysis
law.invention
chemistry.chemical_compound
Colloid and Surface Chemistry
Adsorption
DYNAMIC-NUCLEAR-POLARIZATION
[CHIM.ANAL]Chemical Sciences/Analytical chemistry
law
Molecule
Crystallization
Dissolution
Silicates
Water
Hydrogen Bonding
CORRELATION SPECTROSCOPY
General Chemistry
021001 nanoscience & nanotechnology
Silicate
SOLID-STATE NMR
0104 chemical sciences
chemistry
Heteronuclear molecule
Solid-state nuclear magnetic resonance
13. Climate action
CROSS-POLARIZATION
Particle
Calcium
SI-29 MAS NMR
0210 nano-technology
CRYSTAL-GROWTH
PORTLAND-CEMENT
Subjects
Details
- ISSN :
- 00027863 and 15205126
- Database :
- OpenAIRE
- Journal :
- Journal of the American Chemical Society, Journal of the American Chemical Society, American Chemical Society, 2015, 137 (25), pp.8096-8112. ⟨10.1021/jacs.5b00622⟩, Journal of the American Chemical Society, 2015, 137 (25), pp.8096-8112. ⟨10.1021/jacs.5b00622⟩
- Accession number :
- edsair.doi.dedup.....b3f56a2c5bf07d0cabee75d85ab86381
- Full Text :
- https://doi.org/10.1021/jacs.5b00622⟩