Probing the Mechanisms Underlying Electrolyte-Assisted Nucleation Enhancement of dl-Alanine
Source abstract
Abstract
The effects of common electrolytes (including inorganic acids, bases, and salts) on dl -alanine nucleation in aqueous solutions have been systematically investigated via measurement of nucleation induction times. It is observed that all the electrolytes examined in this study considerably shorten the induction times, suggesting that they greatly enhance dl -alanine nucleation. It is hypothesized that, in solution, an electrolyte assists the formation of the head-to-tail chains of dl -alanine molecules. Such head-to-tail chains, structurally matching dl -alanine crystal packing, act as favorable precursors for dl -alanine nucleation and play a great role in enhancing the nucleation, highlighting the importance of prenucleation phenomena.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Crystallization and Solubility Studies · nanoparticles nucleation surface interactions · Spectroscopy and Quantum Chemical Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Chemical and Engineering Sciences, A-STAR (Agency for Science, Technology and Research), 1, Pesek Road, Jurong Island, Singapore 627833
Department of Chemical and Biomolecular Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260
References (25)
Show source-provided references
1. Huang J. · J. Am. Chem. Soc. · 2008 · 130 · 1397310.1021/ja804836d ↗
2. Weissbuch I. · Adv. Mater. · 1994 · 6 · 95210.1002/adma.19940061211 ↗
3. Towler C. S. · J. Am. Chem. Soc. · 2004 · 126 · 1334710.1021/ja047507k ↗
4. Dowling R. · Chem. Commun. · 2010 · 46 · 592410.1039/c0cc00336k ↗
5. Han G. · CrystEngComm · 2013 · 15 · 121810.1039/c2ce26594j ↗
6. Lee E. H. · Cryst. Growth Des. · 2008 · 8 · 9110.1021/cg7008607 ↗
7. Weissbuch I. · Angew.Chem. Int. Ed. · 2005 · 44 · 322610.1002/anie.200500164 ↗
8. Stoica C. · Cryst. Growth Des. · 2004 · 4 · 76510.1021/cg0342314 ↗
9. Hod I. · CrystEngComm · 2011 · 13 · 50210.1039/C0CE00133C ↗
10. Han G. · Cryst. Growth Des. · 2012 · 12 · 555510.1021/cg301108t ↗
11. Han G. · Cryst. Growth Des. · 2010 · 10 · 488310.1021/cg100934f ↗
12. Li L. · J. Cryst. Growth · 1992 · 121 · 3310.1016/0022-0248(92)90172-F ↗
13. Kubota N. · Cryst. Res. Technol. · 2001 · 36 · 74910.1002/1521-4079(200110)36:8/10<749::AID-CRAT749>3.0.CO;2-# ↗
14. Han G. · Cryst. Growth Des. · 2011 · 11 · 394110.1021/cg2005437 ↗
15. Shimon L. J. W. · J. Am. Chem. Soc. · 1990 · 112 · 621510.1021/ja00173a008 ↗
16. Han G. · Chem. Eng. Sci. · 2009 · 64 · 398310.1016/j.ces.2009.05.040 ↗
17. Friant-Michel P. · ChemPhysChem · 2010 · 11 · 349910.1002/cphc.201000354 ↗
18. Hamad S. · J. Phys. Chem. B · 2008 · 112 · 728010.1021/jp711271z ↗
19. Davey R. J. · Mol. Cryst. Liq. Cryst. Inc. Nonlinear Opt. · 1988 · 161 · 28310.1080/00268948808070253 ↗
20. Ma Y. R. · Chem.—Eur. J. · 2006 · 12 · 788210.1002/chem.200501324 ↗
21. Erdemir D. · Acc. Chem. Res. · 2009 · 42 · 62110.1021/ar800217x ↗
22. Vekilov P. G. · Cryst. Growth Des. · 2010 · 10 · 500710.1021/cg1011633 ↗
23. Han G. · Cryst. Growth Des. · 2012 · 12 · 221310.1021/cg201321f ↗
24. Popovitz-Biro R. · Adv. Mater. · 1994 · 6 · 95610.1002/adma.19940061212 ↗
25. Bourne J. R. · J. Cryst. Growth · 1976 · 36 · 27810.1016/0022-0248(76)90290-6 ↗