OLIGOMERIC CHROMIUM(III) POLICATION SPECIES-PILLARED LAYERED TETRATITANATES ANION
Author(s) -
Hari Sutrisno,
Endang Dwi Siswani
Publication year - 2010
Publication title -
indonesian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.273
H-Index - 14
eISSN - 2460-1578
pISSN - 1411-9420
DOI - 10.22146/ijc.21706
Subject(s) - chemistry , chromium , intercalation (chemistry) , aqueous solution , monoclinic crystal system , crystallography , inorganic chemistry , crystal structure , organic chemistry
Intercalation of oligomeric chromium(III) polycation species in layered tetratitanates was prepared by three steps: 1) ion-exchange of H + for K + in potasium tetratitanates, 2) intercalation of n-alchylamine (n-propylamine, nbutylamine, n-amylamine, and n-hexylamine) compounds in layered hydrogen tetratitanates by adding an aqueous solution of 5M n-alchylamine to hydogen titanates with stiring at room temperature, and 3) intercalation of oligomeric chromium(III) polycation species by mixing butylamine-intercalated tetratitanates with an aqueous solution of CrCl3.6H2O at pH various. The procedure was carried out by Chimie Douce method. The results showed that all of n-alchylamine-intercalated tetratitanates crystallize on monoclinic crystal system with the Bravais lattice C. The hight intensity of the first peaks (200) indicated that butylamine and amylamine-intercalated tetratitanates have a remarkably high crystallinity without impurities phase. The interlayered distance (d) and the lattice parameter projected along a increase with increasing the amount of C-atoms in n-alchylamine. At pH=1.3, [CrCl(H2O)5] 2+ or [CrCl2(H2O)4] + species was pillared more efective in layered tetratitanates than [Cr(H2O)6] 3+ spesies and just one spesies, Cr(H2O)6] 3+ at pH=1.7. On the contrary, [Cr(OH)(H2O)5] 2+ or [Cr(OH)2(H2O)4] + was intercalated more effevtive than [Cr(H2O)6] 3+ species at pH=5.3.
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