Effect of cationic polyelectrolytes addition in cement cohesion
Here is studied the variation in cohesion of cement main phase (C-S-H) as a result of cationic polyelectrolytes addition (quaternary amines spermine and norspermidine). Cohesion study was carried out by molecular simulation techniques (Monte Carlo) using a primitive model in a canonical ensemble (NV...
- Autores:
-
Zuluaga-Hernández, Edison Albert
Hoyos, Bibian A.
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2014
- Institución:
- Universidad Nacional de Colombia
- Repositorio:
- Universidad Nacional de Colombia
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unal.edu.co:unal/52526
- Acceso en línea:
- https://repositorio.unal.edu.co/handle/unal/52526
http://bdigital.unal.edu.co/46872/
- Palabra clave:
- cement cohesion
molecular simulation
cationic polyelectrolytes
osmotic pressure
primitive model.
- Rights
- openAccess
- License
- Atribución-NoComercial 4.0 Internacional
Summary: | Here is studied the variation in cohesion of cement main phase (C-S-H) as a result of cationic polyelectrolytes addition (quaternary amines spermine and norspermidine). Cohesion study was carried out by molecular simulation techniques (Monte Carlo) using a primitive model in a canonical ensemble (NVT). The proposed model takes into account the influence of ionic size of each particle and the addition of polyelectrolytes with different charge number and separation. The results obtained show that electrostatic interactions are responsible for the cohesion of the hardened cement. It was found that in absence of cationic polyelectrolytes, cohesion is lost when the C-S-H lamellae are at separations larger than 1 nm. Adding cationic polyelectrolytes generates a distribution of hydroxide ions around the polyelectrolyte charges, facilitates the distribution of calcium and sodium ions in the entire space between C-S-H surfaces; this allows the cohesive forces exist at greater distances of separation between the surfaces. |
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