scholarly journals Isolation and physico-chemical characterization of lignins from ultrasound irradiated fast-growing poplar wood

BioResources ◽  
2010 ◽  
Vol 6 (1) ◽  
pp. 414-433
Author(s):  
Tong-Qi Yuan ◽  
Shaoni Sun ◽  
Feng Xu ◽  
Run-Cang Sun

Ultrasonic irradiation with organic solvents and alkaline extractions were carried out on a fast-growing poplar wood, triploid of Populus tomentosa Carr., in an attempt to develop efficient lignin isolation procedures. Four organosolv and three alkaline lignin fractions were successively isolated and comparatively characterized by sugar analysis, alkaline nitrobenzene oxidation, gel permeation chromatography (GPC), Fourier transform infra-red spectroscopy (FT-IR), quantitative 13C, and 2D HSQC nuclear magnetic resonance (NMR) spectroscopy, as well as thermogravimetric analysis (TGA). The results showed that the ultrasonic treatments and sequential extractions with three different concentrations of NaOH led to a release of 90.9% of the original lignin. The four organosolv lignin preparations obtained under the ultrasound-assisted extractions were degraded significantly and contained more carbohydrate and non-condensed syringyl units when compared to the three alkaline lignin preparations. Furthermore, the analyses confirmed that L5, the lignin preparation with the highest yield (44.6% of the original lignin), was partially acylated at the γ-carbon of the side-chain preferentially over syringyl units. The percentage of lignin acylation of β-O-4’ linkages was about 14%. The amount of β-O-4’, β-β’, and –OCH3 were estimated to be about 0.31/Ar, 0.06/Ar, and 1.73/Ar, respectively. The ratio of S/G was calculated to be 2.0.

2011 ◽  
Vol 299-300 ◽  
pp. 747-750
Author(s):  
Li Hong Zhao ◽  
Hong Jun Sun

The physico-chemical characterization of two types of alkali lignin from different origin, namely L1 and L2, were studied by Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance spectrometry (1H NMR) and gel permeation chromatography (GPC) analysis. FT-IR spectra show that they have the characteristics of absorption peaks of syringyl and guaiacyl. 1H NMR spectra indicate that acetylated L1 exhibits higher content of aromatic protons than L2, as the former is mainly composed by G units. L2 presents high quantities of methoxyl groups. GPC results show that L1 has much higher weight average than L2. They had similar functional groups, however, there were differences in the relative contents of functional groups.


Alergologia ◽  
2020 ◽  
Vol 1 (4) ◽  
pp. 7
Author(s):  
Mariana Vieru ◽  
Florin-Dan Popescu ◽  
Laura Haidar ◽  
Carmen Bunu-Panaitescu

2010 ◽  
Vol 35 (5) ◽  
pp. 261-267 ◽  
Author(s):  
Wissemn Gallala ◽  
Mohamed Essghaier Gaied ◽  
Borhen Kchaou

2001 ◽  
Vol 71 (3) ◽  
pp. 342-349
Author(s):  
Lucian Eva ◽  
Letitia Doina Duceac ◽  
Liviu Stafie ◽  
Constantin Marcu ◽  
Geta Mitrea ◽  
...  

The fourth generation cephalosporin antibacterial agent, cefepime, was loaded into layered double hydroxides for enhancing antibiotic efficiency, reducing side effects, as well as achieving the sustained release property. The intercalation of antibiotic into the inter-gallery of ZnAl-layered double hydroxide (LDH) was carried out using ion exchange method, by this constituting a nano-sized organic-inorganic hybrid material for a controlled release novel formulation. Although cefepime is a broad spectrum antibiotic, it has various adverse effects and a significant degradation rate. Thus, the preparation and physico-chemical characterization of nanomaterials able to intercalate this drug is an important study for medical and pharmaceutical field. The antibiotic inclusion into LDHs nanostructure was confirmed by advanced characterization techniques and the release profile of cefepime was analysed with the respect to pH of the simulated media.


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