Document Detail


A comparison study of rhodamine B photodegradation over nitrogen-doped lamellar niobic acid and titanic acid under visible-light irradiation.
MedLine Citation:
PMID:  19206115     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
A solid-state reaction method with urea as a nitrogen precursor was used to prepare nitrogen-doped lamellar niobic and titanic solid acids (i.e., HNb(3)O(8) and H(2)Ti(4)O(9)) with different acidities for visible-light photocatalysis. The photocatalytic activities of the nitrogen-doped solid acids were evaluated for rhodamine B (RhB) degradation and the results were compared with those obtained over the corresponding nitrogen-doped potassium salts. Techniques such as XRD, BET, SEM, X-ray photoelectron spectroscopy, and UV-visible diffuse reflectance spectroscopy were adopted to explore the nature of the materials as well as the characteristics of the doped nitrogen species. It was found that the intercalation of the urea precursor helped to stabilize the layered structures of both lamellar solid acids and enabled easier nitrogen doping. The effects of urea intercalation were more significant for the more acidic HNb(3)O(8) sample than for the less acidic H(2)Ti(4)O(9). Compared with the nitrogen-doped KNb(3)O(8) and K(2)Ti(4)O(9) samples, the nitrogen-doped HNb(3)O(8) and H(2)Ti(4)O(9) solid acids absorb more visible light and exhibit a superior activity for RhB photodegradation under visible-light irradiation. The nitrogen-doped HNb(3)O(8) sample performed the best among all the samples. The results of the current study suggest that the protonic acidity of the lamellar solid-acid sample is a key factor that influences nitrogen doping and the resultant visible-light photocatalysis.
Authors:
Xiukai Li; Naoki Kikugawa; Jinhua Ye
Related Documents :
998545 - Plasma amino acids and nitrogen retention of human subjects who consumed isonitrogenous...
22655455 - Dietary trans fatty acids intake and its relation to dyslipidemia in a sample of adults...
14623605 - Hydroxamic acids: proton donor and acceptor strength for use in drug design.
8730615 - A 15n-leucine-dilution method to measure endogenous contribution to luminal nitrogen in...
7060885 - Response of total and individual serum bile acids to endogenous and exogenous bile acid...
14523555 - Notable diversity in hemoglobin expression patterns among species of the deep-sea clam,...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Chemistry (Weinheim an der Bergstrasse, Germany)     Volume:  15     ISSN:  1521-3765     ISO Abbreviation:  Chemistry     Publication Date:  2009  
Date Detail:
Created Date:  2009-03-30     Completed Date:  2009-05-19     Revised Date:  2009-08-04    
Medline Journal Info:
Nlm Unique ID:  9513783     Medline TA:  Chemistry     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  3538-45     Citation Subset:  -    
Affiliation:
International Center for Materials Nanoarchitectonics, Photocatalytic Materials Center (PCMC), National Institute for Materials Science (NIMS), 1-2-1 Sengen, Tsukuba, Ibaraki, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Bioinspired supramolecular confinement of luminol and heme proteins to enhance the chemiluminescent ...
Next Document:  Towards controlling the threading direction of a calix[6]arene wheel by using nonsymmetric axles.