Complexation of arsenate to humic acid with different molecular weight fractions in aqueous solution

Author(s):  
Shifeng Li ◽  
Feng Lu ◽  
Hongtao Lv ◽  
Yang Zhou ◽  
Mario A. Gomez ◽  
...  
1977 ◽  
Vol 23 (4) ◽  
pp. 434-440 ◽  
Author(s):  
Don L. Crawford ◽  
Suellen Floyd ◽  
Anthony L. Pometto III ◽  
Ronald L. Crawford

The comparative rates of microbial degradation 14C-lignin-labeled lignocelluloses and 14C-Kraft lignins were investigated using selected soil and water samples as sources of microorganisms. Natural lignocelluloses containing 14C primarily in their lignin components were prepared by feeding plants uniformly labeled L-[14C]phenylalanine through their cut stems. 14C-Kraft lignins were prepared by pulping lignin-labeled lignocelluloses. Rates of lignin biodegradation were determined by monitoring 14CO2 evolution from incubation mixtures over incubation periods of up to 1000 h. Observed rates of lignin degradation were slow in all cases. Kraft lignins appeared more resistant to microbial attack than natural lignins, even though they were decomposed more rapidly during the first 100–200 h of incubation. Similar degradation patterns were observed in both soil and water. Individual samples, however, varied greatly in their overall rates of degradation of either lignin type. A Kraft-lignin preparation was separated into a variety of molecular weight fractions by column chromatography on LH-20 Sephadex and the biodegradability of the different molecular weight fractions determined. The lower molecular weight fractions of the Kraft lignin were decomposed at a significantly faster rate by the microflora of soil than were the fractions of higher molecular weight.


2017 ◽  
Vol 70 (3) ◽  
pp. 322 ◽  
Author(s):  
Sachiko Yamanaka ◽  
Koichi Yoshioka ◽  
Hisashi Miyafuji ◽  
Hiroyuki Ohno

We successfully dissolved cedar powder with tetrabutylphosphonium hydroxide ([P4 4 4 4]OH) aqueous solution at 60°C. The dissolution was accelerated by the addition of H2O2. At the initial stage, cellulose was more soluble than hemicellulose and lignin. Both hemicellulose and lignin were gradually dissolved in this solution containing H2O2. Cellulose chains were revealed to be cut into shorter chains in this solution. The lignin network was also found to be partly broken at 60°C. These steps induced components with higher-molecular-weight fractions that cannot be extracted with polar ionic liquids to dissolve. Also, low-molecular-weight fractions such as vanillin and 5-(hydroxymethyl)furfural were found in the resulting solution. Breakage of ether bonds of polysaccharides and lignin and further oxidation were attributed to the active oxygens generated from H2O2. The aqueous mixture reported here is a protocol that can be used to dissolve woody biomass under mild conditions.


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