High-temperature alkaline stability of cement set retarders and their performance at 70–90°C
Source abstract
Abstract
Hydroxycarboxylic acid salt (sodium gluconate), sodium lignosulfonate and a combination of carboxylic acid and sulfonate-type retarder (poly(4-styrenesulfonic acid-co-maleic acid) sodium salt) are typical set retarders for oil-well cement. The potential high-temperature alkali degradation of these retarders is assessed, and its role in altering the kinetics of cement hydration at temperatures between 70 and 90°C. The high-temperature alkaline stability of cement set retarders is poorly studied. However, it may represent one way to understand the delay in hydration induced by such additives, and the discontinuity of cement hydration, with the longer setting times at higher temperatures in that range. Degradation products are identified and their thermal stability is evaluated. Retarders containing carboxylic acid become partially fragmented at high pH and 90°C. The effect on cement setting kinetics is similar for hydrolysed retarders containing carboxylic acid groups: the setting times are longer at 80°C than at 70 and 90°C. The sulfonate groups of lignosulfonate-type retarder, treated at pH 13·4, 90°C, are partially converted to sulfate and the ether groups to alkoxides. The setting time changes linearly with temperature for the high-pH-treated lignosulfonate retarder in the studied temperature range.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Concrete and Cement Materials Research · Materials Engineering and Processing · Magnesium Oxide Properties and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Scientist, Sustainable Energy Technologies Department, Brookhaven National Laboratory, Upton, New York, USA
Chemist, Sustainable Energy Technologies Department, Brookhaven National Laboratory, Upton, New York, USA
References (33)
Show source-provided references
1. 10.1016/j.indcrop.2004.04.02210.1016/j.indcrop.2004.04.022 ↗
2. Cai LJ · Nanotechnology · 2011 · 22 · 1
3. Collepardi MM · 1995 · 286
4. 10.1016/S0371-1951(56)80102-110.1016/S0371-1951(56)80102-1 ↗
5. Escandar GM · Polyhedron · 1995 · 15 · 225110.1016/0277-5387(95)00478-5 ↗
6. Hrehorova E · 2005 · 197
7. 10.1016/j.elspec.2005.05.00610.1016/j.elspec.2005.05.006 ↗
8. 10.1590/S0100-4670200600030000210.1590/S0100-46702006000300002 ↗
9. 10.1016/S0016-7037(99)00194-510.1016/S0016-7037(99)00194-5 ↗
10. 10.1016/j.biombioe.2012.06.00510.1016/j.biombioe.2012.06.005 ↗
11. 10.1016/j.tca.2008.09.00310.1016/j.tca.2008.09.003 ↗
12. 10.1155/2009/85921810.1155/2009/859218 ↗
13. 10.1016/0040-6031(81)80175-X10.1016/0040-6031(81)80175-X ↗
14. Nakanishi K · 1977
15. Nelson E · 2006
16. 10.1016/0008-8846(78)90027-310.1016/0008-8846(78)90027-3 ↗
17. 10.1016/0008-8846(78)90034-010.1016/0008-8846(78)90034-0 ↗
18. 10.1346/CCMN.1997.045020710.1346/CCMN.1997.0450207 ↗
19. 10.1016/j.saa.2005.06.04810.1016/j.saa.2005.06.048 ↗
20. 10.1139/v68-04010.1139/v68-040 ↗
21. 10.1016/j.cemconres.2006.03.02810.1016/j.cemconres.2006.03.028 ↗
22. 10.1016/S0927-7757(03)00063-310.1016/S0927-7757(03)00063-3 ↗
23. 10.1016/j.memsci.2008.04.00410.1016/j.memsci.2008.04.004 ↗
24. 10.1002/jrs.70110.1002/jrs.701 ↗
25. 10.1016/S0014-3057(01)00020-910.1016/S0014-3057(01)00020-9 ↗
26. 10.1039/b105712j10.1039/b105712j ↗
27. 10.1016/0162-0134(88)80017-510.1016/0162-0134(88)80017-5 ↗
28. 10.1680/cc.2592910.1680/cc.25929 ↗
29. 10.1016/j.eurpolymj.2009.10.00310.1016/j.eurpolymj.2009.10.003 ↗
30. 10.1016/S0969-806X(99)00519-810.1016/S0969-806X(99)00519-8 ↗
31. 10.1016/0368-2048(90)80271-B10.1016/0368-2048(90)80271-B ↗
32. 10.1002/ep.1043310.1002/ep.10433 ↗
33. 10.1016/j.tca.2011.11.00310.1016/j.tca.2011.11.003 ↗