scholarly journals Molecular Characteristics and Antioxidant Activity of Spruce (Picea abies) Hemicelluloses Isolated by Catalytic Oxidative Delignification

Molecules ◽  
2022 ◽  
Vol 27 (1) ◽  
pp. 266
Author(s):  
Valentina S. Borovkova ◽  
Yuriy N. Malyar ◽  
Irina G. Sudakova ◽  
Anna I. Chudina ◽  
Andrey M. Skripnikov ◽  
...  

Spruce (Piceaabies) wood hemicelluloses have been obtained by the noncatalytic and catalytic oxidative delignification in the acetic acid-water-hydrogen peroxide medium in a processing time of 3–4 h and temperatures of 90–100 °C. In the catalytic process, the H2SO4, MnSO4, TiO2, and (NH4)6Mo7O24 catalysts have been used. A polysaccharide yield of up to 11.7 wt% has been found. The hemicellulose composition and structure have been studied by a complex of physicochemical methods, including gas and gel permeation chromatography, Fourier-transform infrared spectroscopy, and thermogravimetric analysis. The galactose:mannose:glucose:arabinose:xylose monomeric units in a ratio of 5:3:2:1:1 have been identified in the hemicelluloses by gas chromatography. Using gel permeation chromatography, the weight average molar mass Mw of hemicelluloses has been found to attain 47,654 g/mol in noncatalytic delignification and up to 42,793 g/mol in catalytic delignification. Based on the same technique, a method for determining the α and k parameters of the Mark–Kuhn–Houwink equation for hemicelluloses has been developed; it has been established that these parameters change between 0.33–1.01 and 1.57–472.17, respectively, depending on the catalyst concentration and process temperature and time. Moreover, the FTIR spectra of the hemicellulose samples contain all the bands characteristic of heteropolysaccharides, specifically, 1069 cm−1 (C–O–C and C–O–H), 1738 cm−1 (ester C=O), 1375 cm−1 (–C–CH3), 1243 cm−1 (–C–O–), etc. It has been determined by the thermogravimetric analysis that the hemicelluloses isolated from spruce wood are resistant to heating to temperatures of up to ~100 °C and, upon further heating, start destructing at an increasing rate. The antioxidant activity of the hemicelluloses has been examined using the compounds simulating the 2,2-diphenyl-2-picrylhydrazyl free radicals.

1984 ◽  
Vol 49 (10) ◽  
pp. 2197-2204 ◽  
Author(s):  
Miroslav Kubín

The validity of the effective linear calibration (ELC) method in gel permeation chromatography of polymers has been checked by means of computer generated chromatograms. The ratio Mw/Mn calculated using ELC form an uncorrected chromatogram is always smaller than that determined by means of the true calibration dependence, but the extent of this correction for longitudinal spreading depends on the polydispersity of both the original calibration standard and the analyzed polymer, and also on the separation efficiency of the given column. If the respective molecular weight averages of the analyzed sample and of the calibration standard differ considerably, the effective linear calibration method leads to serious systematic errors in the calculated average molar mass values.


Processes ◽  
2020 ◽  
Vol 8 (7) ◽  
pp. 860 ◽  
Author(s):  
Anna Trubetskaya ◽  
Heiko Lange ◽  
Bernd Wittgens ◽  
Anders Brunsvik ◽  
Claudia Crestini ◽  
...  

This study demonstrates the effects of structural variations of lignins isolated via an organosolv process from different woody and herbaceous feedstocks on their thermal stability profiles. The organosolv lignins were first analysed for impurities, and structural features were determined using the default set of gel permeation chromatography, FT-IR spectroscopy, quantitative 31 P NMR spectroscopy and semi-quantitative 1 H- 13 C HSQC analysis. Pyrolysis-, O 2 - and CO 2 -reactivity of the organosolv lignins were investigated by thermogravimetric analysis (TGA), and volatile formation in various heating cycles was mapped by head-space GC-MS analysis. Revealed reactivities were correlated to the presence of identified impurities and structural features typical for the organosolv lignins. Data suggest that thermogravimetric analysis can eventually be used to delineate a lignin character when basic information regarding its isolation method is available.


2019 ◽  
Vol 85 (6) ◽  
pp. 87-96
Author(s):  
Nadiia Ivakha ◽  
Oleksandr Rohovtsov ◽  
Oleksandra Berezhnytska ◽  
Elena Trunova

In this work, the new coordination compounds of Nd(III) and Er (III) with b-diketonate ligands containing an unsaturated substituent at the a-position of the chelate ring (dimethylheptendione and dimethyloctendione) were synthesized. The composition and structure of the synthesized compounds were studied using physicochemical methods of analysis such as the elemental, NMR, IR and electron spectroscopy and thermogravimetric analysis. Using IR spectroscopy, it was established that ligands are bidentate-cyclically coordinated to metals. The results of thermogravimetric analysis indicate that the complexes are nonvolatile and decompose to oxides of the corresponding metals, and their coordination sphere is supplemented with water molecules. From the shape and position of the bands in the electronic absorption spectra and diffuse reflection spectra, it was determined that for the complexes Ln (b-dik)3.nH2O (Ln =Nd, Er,  b-dik = dmhpd, dmod, n = 2-3) the tetragonal symmetry of the nearest coordination environment; coordination polyhedron is a square antiprism. When comparing the diffuse reflectance spectra of dimethylheptendionate and dimethyloktendionate complexes among themselves and with the previously studied complexes with methacrylacetophenone, it was noted that the shape of the spectra and the spectral splitting of the bands for the corresponding metals are not significantly different. This allows to conclude, that the coordination environment of the studied b-diketonate compounds is close.Based on the band shifts in the electronic spectra, the covalence parameters of the Ln–O bond and the oscillator strength were calculated, from which it was also shown that the nature of the substituent affects the covalence parameters, but does not affect the symmetry and structure of the coordination polyhedron. Based on the studies conducted, the monomeric structure of the synthesized complexes was definitely confirmed. Accordingly, they can be used in further work as monomers in polymerization reactions and the preparation of precursors of luminescent materials.


1989 ◽  
Vol 31 (3) ◽  
pp. 654-660
Author(s):  
N.A. Domnicheva ◽  
S.I. Kogan ◽  
V.A. Kuznetsova ◽  
A.Ya. Sorokin ◽  
V.P. Budtov

2018 ◽  
Vol 45 (1) ◽  
pp. 27-30
Author(s):  
N.A. Shabunina ◽  
V.D. Voronchikhin ◽  
E.I. Lesik ◽  
A.V. Berestyuk ◽  
O.V. Karmanova ◽  
...  

Using methods of IR spectroscopy (Fourier infrared spectrometer; PerkinElmer) and gel permeation chromatography (Agilent 1200; Agilent Technologies), we studied the microstructure and molecular characteristics of four types of diene oligomer (DO) of different functionality. The dynamic viscosity, η, of DOs was measured on a rotary viscometer (LVDV-II + Pro; Brookfield). A comparative analysis of the obtained results makes it possible to predict the dispersion and the plasticising effect of DOs in polymer–oligomer composites. The temperature dependences of η for different DOs differ in the temperature range 20–60°C; at temperatures of 80°C and above, the values of h are practically identical, i.e. their processing properties are the same, and the replacement of one DO with another will not lead to any need to alter the processing regime of the composites.


2008 ◽  
Vol 63 (3-4) ◽  
pp. 181-188 ◽  
Author(s):  
Feng He ◽  
Ying Yang ◽  
Guang Yang ◽  
Longjiang Yu

A polysaccharide was isolated from the broth of cultured Streptomyces virginia H03 which was treated by ethanol deposition and savage method to remove the protein, and was purified using Sephadex G-150 column chromatography. The components of the polysaccharide were determined by gas chromatography. The purified polysaccharide was made up of mannose, glucose and galactose, in a 2:1:1 proportion. Its average apparent molecular weight was 3.76 · 104 Da which was determined by gel permeation chromatography. In addition, several antioxidant assays were adopted to investigate the antioxidant activity of the polysaccharide in vitro. The results indicated that the purified polysaccharide showed significant antioxidant activity against superoxide anion, hydrogen peroxide and 1,1-diphenyl-2-picrylhydrazyl radical, and lipid peroxidation as with standard antioxidants such as vitamin C. Furthermore, the polysaccharide had a better heat stability than vitamin C, which suggested that the polysaccharide might be a potent useful antioxidant


2021 ◽  
Vol 50 (6) ◽  
pp. 1767-1773
Author(s):  
Manjusha Elizabeth Mathew ◽  
Ishak Ahmad ◽  
Sabu Thomas ◽  
Muhammad Kassim ◽  
Rusli Daik

Polyvinyl benzyl chloride (PVBC) was synthesized by free radical polymerization of 4-vinylbenzyl chloride using benzoyl peroxide initiator at 60 °C. PVBC was synthesised in different solvents such as toluene, xylene, 1,4-dioxane, and tetrahydrofuran. The polymers were structurally characterized by 1H NMR and FTIR spectroscopic techniques. The thermal property of the polymer was investigated by thermogravimetric analysis (TGA) and differential thermogravimetric analysis (DTA).The number average molecular weight, weight average molecular weight and polydispersity index of PVBC synthesised in different solvents were determined and compared by gel permeation chromatography technique.


Polymers ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 285
Author(s):  
Yulia S. Dyuzhikova ◽  
Anton A. Anisimov ◽  
Alexander S. Peregudov ◽  
Mikhail I. Buzin ◽  
Galina G. Nikiforova ◽  
...  

New non-crystallizable low-dispersity star-shaped polydimethylsiloxanes (PDMS) containing stereoregular cis-tetra(organo)(dimethylsiloxy)cyclotetrasiloxanes containing methyl-, tolyl- and phenyl-substituents at silicon atoms and the mixture of four stereoisomers of tetra[phenyl(dimethylsiloxy)]cyclotetrasiloxane as the cores were synthesized. Their thermal and viscous properties were studied. All synthesized compounds were characterized by a complex of physicochemical analysis methods: nuclear magnetic resonance (NMR), FT-IR spectroscopy, gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), viscometry in solution, rheometry, and Langmuir trough study.


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