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  4. Interactions of the products of oxidative polymerization of hydroquinone as catalyzed by birnessite with Fe (hydr)oxides-an implication of the reactive pathway for humic substance formation
 
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Interactions of the products of oxidative polymerization of hydroquinone as catalyzed by birnessite with Fe (hydr)oxides-an implication of the reactive pathway for humic substance formation

Journal
RSC Advances
Journal Volume
6
Journal Volume
6
Journal Issue
25
Journal Issue
25
Pages
20750-20760
Start Page
20750
End Page
20760
ISSN
20462069
Date Issued
2016
Author(s)
Chang R.R.
SHAN-LI WANG  
Liu Y.T.
Chan Y.T.
Hung J.T.
Tzou Y.M.
Tseng K.J.
DOI
10.1039/c5ra19734a
URI
https://www.scopus.com/pages/publications/84975767780?origin=resultslist
URL
https://www2.scopus.com/inward/record.uri?eid=2-s2.0-84975767780&doi=10.1039%2fc5ra19734a&partnerID=40&md5=c805723736b80b2cef77168d4b380feb
Abstract
Polyphenol polymerization (PP) catalyzed by MnO2 is an important pathway in humification processes in soils. Due to a lack of aliphatic carbons, the products of PP are considered to be humic substance-like materials (HQs), which are subject to adsorption by Fe (hydr)oxide upon their formation. However, the effects of the interactions of HQs with Fe (hydr)oxide in humification processes have received less attention. In this study, hydroquinone was reacted with birnessite for 1 d (HQ-1). After the removal of residual birnessite, the filtrates were incubated for another 7 and 20 days and were denoted as HQ-7, and HQ-20, respectively. The spectroscopic analyses of the HQ samples indicated that oxidative polymerization of hydroquinone occurred within 1 d. With an increase in incubation time, the molecular structure of the resultant HQ continued to change and became increasingly similar to that of natural humic acid (HA), even in the absence of birnessite. Upon adsorption of the HQs by Fe (hydr)oxide, changes in the IR absorption band indicated the complexation of HQ carboxyl groups with metal centers on the mineral surfaces. HQ-20 was preferentially adsorbed on the Fe (hydr)oxides because it contained a higher number of carboxyl groups than their counterparts with a smaller molecular weight. In addition, the steric arrangements and the distributions of the adsorption sites on Fe (hydr)oxide, closely matching the structures of larger molecules, may also contribute to the preferential adsorption. This study implies that HQs with a larger molecular size can be accumulated in soils while reacting with Fe (hydr)oxides during their formation, and the association of HQs with aliphatic carbons derived from the Maillard reaction may contribute to humic substance (HS) formation.
Publisher
Royal Society of Chemistry
Type
journal article

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