Spectroscopic and chemical characterizations of molecular size fractionated humic acid

Talanta ◽  
1999 ◽  
Vol 50 (3) ◽  
pp. 641-647 ◽  
Author(s):  
H Shin
Keyword(s):  
2003 ◽  
Vol 47 (1) ◽  
pp. 89-95 ◽  
Author(s):  
J. Yu ◽  
D.D. Sun ◽  
J.H. Tay

Ferric chloride and aluminium sulphate as coagulants and positive charged flocculants PDDMAC ((PDDMAC = poly (diallyldimethylammonium chloride) were used for pre-treatment of water and wastewater for removing humic substance prior to RO membrane filtration. It was found that a combination of flocculant and coagulant enhanced the coagulation-flocculation process and humic acid removal. The optimum conditions of coagulation-flocculation were established in reference to the ratio of humic acid and coagulant. Zeta potential and the ratio of E4/E6 were investigated to explore the possible micro-mechanisms of coagulation-flocculation. The ratios of E4/E6 show the molecular size variations using different coagulants and flocculants, which are expected to benefit membrane-fouling control.


2019 ◽  
Vol 38 (6) ◽  
pp. 863-871 ◽  
Author(s):  
Mohamed E. A. El-Sayed ◽  
Moustafa M. R. Khalaf ◽  
James A. Rice

2015 ◽  
Vol 57 (6) ◽  
pp. 2455-2465 ◽  
Author(s):  
P. Akan ◽  
N.C. Birben ◽  
M. Bekbolet

2011 ◽  
Vol 11 (6) ◽  
pp. 692-698 ◽  
Author(s):  
S. Valencia ◽  
J. Marín ◽  
G. Restrepo ◽  
F. H. Frimmel

Much research has been undertaken on the photocatalytic degradation of humic substances with titanium dioxide using commercial humic acids (HA), which are extracts from either peat or coal. Most of the research has been focused on the changes in dissolved organic carbon (DOC) and UV254 absorption. These parameters only give a general assessment. This work studies the changes in the physical and structural properties of a commercial humic acid by size exclusion chromatography with DOC and UV254 absorption detection (SEC-DOC, SEC-UV254), and the evolution of halogenated organic compounds (AOX) and trihalomethanes (THMs) during the photocatalytic degradation with simulated solar UV irradiation and Degussa P-25 TiO2. These changes are compared with those reported for natural organic matter (NOM). The photodegradation of commercial HA and NOM proceeds in a similar and sequential manner, initially with the preferential adsorption of larger molecules, then the degradation of these larger molecular size fractions and proceeding towards smaller molecular size fractions, while decreasing THMs and AOX formation potential.


1994 ◽  
Vol 353 ◽  
Author(s):  
Tadao Tanaka ◽  
Muneaki Senoo

AbstractSorption experiments have been performed by a batch method, to study the effects of humic acid of different molecular size on the complexing stability with 60Co, 85Sr, 137Cs, 237Np and 241Am, and on the sorption behavior of these radionuclides on a sandy soil.Equilibrium constants K in the sorption of 137Cs and 237Np onto the soil were not changed at different concentrations of humic acid since 137Cs and 237Np do not interact with humic acid, while those of 60Co and 241Am decreased with increasing humic acid concentration due to forming humic complexes. However, the K of 85Sr was not changed at different humic acid concentrations, despite 85Sr interacts with humic acid. This contradiction was probably caused from that a main binding of 85Sr with humic acid is not based on coordination bond but electrostatic force, due to relatively high concentration of non–radioactive strontium. The theoretical sorption model taking account of the interaction of 60Co and 241Am with humic acid could well reproduce the values of K for each radionuclide at different concentrations of humic acid.Concentration profiles of the radionuclides in each size fraction of the solution before and after the sorption experiments were examined by ultrafiltration technique. The reduction of concentration of 60Co in the fraction less than 300,000 of cutoff molecular weight (MW) and that of concentration of 241Am in the fraction larger than 100,000MW, respectively, by the sorption onto the soil decreased with increasing humic acid concentration. This decrease resulted in the decrease in the K of 60Co and 241Am with increasing humic acid concentration.


2010 ◽  
Vol 61 (10) ◽  
pp. 2581-2590 ◽  
Author(s):  
C. S. Uyguner ◽  
M. Bekbolet

The present study investigated the removal efficiency of aqueous humic acid solutions by TiO2 photocatalytic degradation in the presence of Cu(II) species. The pseudo-first-order kinetics revealed rate constants as 9.87 × 10−3, 7.19 × 10−3, 3.81 × 10−3 min−1 for Color436, UV254 and TOC, respectively. Comparatively, lower rate constants were attained with respect to photocatalytic degradation of humic acid. Considering the source-dependent diverse chemical and spectral characteristics of NOM, a particular interaction would be expected for humic acid with Cu(II) species (0.1 mg L−1). The presence of copper ions significantly altered the photocatalytic degradation kinetics of humic acids in relation to the concentration effects of humic acid as expressed by spectroscopic parameters and TOC. Batch equilibrium adsorption experiments revealed a distinct Langmuirian-type adsorptive behavior of humic acid onto TiO2 both in terms of UV254 and Color436 and a C-type adsorption isotherm was attained for TOC. KF values displayed an inconsistent effect of Cu(II) species, while adsorption intensity factor 1/n<1 denoted a prevailing favorable type of adsorption for Color436 and UV254. Because of the role of intra- and intermolecular interactions between copper ions and humic molecular size fractions, spectroscopic techniques were also employed for the assessment of the adsorption as well as photocatalytic degradation efficiencies.


2015 ◽  
Vol 14 (3) ◽  
pp. 576-582 ◽  
Author(s):  
M. Bekbolet ◽  
S. Sen-Kavurmaci

Photocatalytic oxidation leads to a drastic change in excitation emission matrix (EEM) fluorescence features of humic acid molecular size fractions.


Geoderma ◽  
2011 ◽  
Vol 163 (1-2) ◽  
pp. 24-29 ◽  
Author(s):  
Claire Richard ◽  
Christian Coelho ◽  
Ghislain Guyot ◽  
Lubov Shaloiko ◽  
Oleg Trubetskoj ◽  
...  

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