Tetrahydrofuran Hydrate Crystal Growth Inhibitor Performance and Mechanism of Quaternary Ammonium and Phosphonium Salts
Source abstract
Abstract
To gain insight into the hydrate crystal growth inhibitor (HCGIs) mechanism, we have studied various quaternary ammonium ionic liquid salts (QAILs) and phosphonium salts for their ability to prevent structure II (sII) hydrate crystal growth. We tested polyvinylpyrrolidone (PVP), polyvinylcaprolactam (PVCap), tetrapropylammonium bromide (TPrAB), tetrabutylammonium bromide (TBAB), tetrapentylammonium bromide (TPeAB), tetrahexylammonium bromide (THexAB), and tetrabutylphosphonium bromide (TBPB) in a tetrahydrofuran (THF) sII hydrate system using a unidirectional growth apparatus to determine the concentration and growth rate dependence. The growth rates of TPrAB, TBAB, and THexAB were found to be critical in the region of low growth rate, with the degree of supercooling ΔT becoming 0 for these additives in the low-growth-rate region. In contrast, PVP, PVCap, TPeAB, and TBPB remained effective at the lowest growth rate of V = 0.04 μm s–1. These trends can be explained by the residence time on the crystal surface of the HCGI, τ, and duration time of crystal growth.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Methane Hydrates and Related Phenomena · Inorganic Fluorides and Related Compounds · Freezing and Crystallization Processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Research Institute of Energy Frontier, National Institute of Advanced Industrial Science and Technology (AIST), Onogawa, Tsukuba, Ibaraki 305-8569, Japan
Department of Chemistry, Bioscience and Environmental Engineering, Faculty of Science and Technology, University of Stavanger, N-4036 Stavanger, Norway
Funding
Japan Society for the Promotion of Science
References (21)
Show source-provided references
1. 10.1021/ef050427x10.1021/ef050427x ↗
2. Kelland M. A. · 2009
3. Klomp, U. C.; Kruka, V. C.; Reijnhart, R. International Patent Application WO/95/17579, 1995.
4. Klomp, U. C.; Reijnhart, R. International Patent Application WO96/34177, 1996.
5. Klomp, U. C.; Kruka, V. C.; Reijnhart, R. Low dosage hydrate inhibitors and how they work. In Proceedings of the symposium Controlling Hydrates, Waxes and Asphaltenes; IBC Conference; Aberdeen; October 1997.
6. Klomp, U. C. International Patent Application, WO99/13197, 1999.
7. Jeffrey, J. Inclusion Compounds; Academic Press; Vol. 1, pp159–190, 1984.10.1007/BF00656757 ↗
8. 10.1007/BF0066324010.1007/BF00663240 ↗
9. 10.1016/j.ces.2011.11.00310.1016/j.ces.2011.11.003 ↗
10. Duncum, S.; Edwards, A. R.; Osborne, C. G. WO Patent Application WO96/04462, 1996.
11. 10.1021/acs.energyfuels.7b0138210.1021/acs.energyfuels.7b01382 ↗
12. 10.1021/acs.jpcc.8b0983410.1021/acs.jpcc.8b09834 ↗
13. Anderson, R.; Mozaffar, H.; Tohidi, B. Development of a Crystal Growth Inhibition Based Method for the Evaluation of Kinetic Hydrate Inhibitors; Proceedings of the 7th International Conference on Gas Hydrates; Edinburgh, Scotland, UK, 2011.
14. 10.1021/acs.energyfuels.6b0273910.1021/acs.energyfuels.6b02739 ↗
15. 10.1016/0009-2509(95)00370-310.1016/0009-2509(95)00370-3 ↗
16. 10.1021/ef201849t10.1021/ef201849t ↗
17. 10.1039/C6RA06122B10.1039/C6RA06122B ↗
18. 10.1039/C9RA00627C10.1039/C9RA00627C ↗
19. 10.1016/j.ces.2016.01.05710.1016/j.ces.2016.01.057 ↗
20. 10.1073/pnas.74.6.258910.1073/pnas.74.6.2589 ↗
21. 10.1016/j.jcrysgro.2004.10.08510.1016/j.jcrysgro.2004.10.085 ↗