Physico-Chemical Characterization of a Fractionated Kraft Lignin

Holzforschung ◽  
2000 ◽  
Vol 54 (5) ◽  
pp. 528-534 ◽  
Author(s):  
Magnus Norgren ◽  
Birger Lindström
Keyword(s):  
Molecular Weight ◽  
Chemical Characterization ◽  
Kraft Lignin ◽  
Size Exclusion ◽  
Median Surface ◽  
Self Diffusion ◽  
Exclusion Chromatography ◽  
Weighted Median ◽  
Phenolic Group ◽  
Pfg Nmr

Summary A kraft lignin was leached from a softwood pulp and fractionated by ultrafiltration. The fractions were characterized in respect to phenolic group content, molecular weight distributions and self-diffusion coefficients. The 1H-Pulsed Field Gradient (PFG) NMR self-diffusion measurements and the High-Pressure Size Exclusion Chromatography (HPSEC) analysis of the fractions, were seen to correlate fairly well. From the self-diffusion measurements, the mass-weighted median hydrodynamic radii of the diffusants in the fractions, were calculated assuming spherical fragments. Furthermore, the content of phenolic groups in the fractions, was found to decrease by increasing hydrodynamic radius and molecular weight, but the calculated median surface charge densities of the macromolecules, were determined to be constant in the range of oligomers up to at least 65 structural units.

Enzymatic polymerization of sodium lignosulfonates: effect of catalysts, initial molecular weight, and mediators

2013 ◽  
Vol 91 (3) ◽  
pp. 220-225 ◽  
Author(s):  
Nidal Madad ◽  
Latifa Chebil ◽  
Celine Charbonnel ◽  
Irina Ioannou ◽  
Mohamed Ghoul
Keyword(s):  
Molecular Weight ◽  
Trametes Versicolor ◽  
Size Exclusion ◽  
Enzymatic Polymerization ◽  
Molecular Weights ◽  
Exclusion Chromatography ◽  
Phenolic Group ◽  
Ft Ir ◽  
Rhus Vernicifera ◽  
Substrate Concentrations

The aim of this study was to investigate the effect of different parameters on the enzymatic polymerization of sodium lignosulfonates (SLS) by laccase, compared with the chemical treatment by manganese III. Different initial molecular weights of SLS (commercial SLS (17 800 Da), F1 (4300 Da), F2 (2500 Da), and F3 (2300 Da)) were tested. Size exclusion chromatography (SEC-UV), Fourier transform infrared (FT-IR) and phenolic group determination showed that SLS molecular weight increases depending on the laccase origin, the enzyme, and the substrate concentrations and the initial molecular weight of the SLS fractions. The highest molecular weight (Mw) was obtained by fungal laccases, specifically when using laccase from Trametes versicolor, while no reactivity was observed by plant laccase (laccase from Rhus vernicifera). The largest increase of Mw (108 600 Da) is reached when using SLS (17 800 Da) at 50 g/L and 30 U/mL of laccase from Trametes versicolor. The laccase polymerization of SLS can be improved by the use of a mediator. In this study, 5 mediators were studied for F1 polymerization by laccase from Trametes versicolor: acetosyringone (ASG), violuric acid (VLA), 1-hydroxy-benzotriazole (HBT), acetovanillone (ACV) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). Results of F1 polymerization with mediators showed that only ASG and VLA lead to a higher molecular weight (7500 Da) compared with reactions carried without a mediator (6600 Da).

Characterisation of Persistent Anti-Xa Activity Following Administration of the Low Molecular Weight Heparin Enoxaparin Sodium (Clexane)

1994 ◽  
Vol 72 (02) ◽  
pp. 275-280 ◽  
Author(s):  
David Brieger ◽  
Joan Dawes
Keyword(s):  
Molecular Weight ◽  
Enoxaparin Sodium ◽  
Antithrombin Iii ◽  
Anticoagulant Activity ◽  
Active Material ◽  
Biologically Active ◽  
Size Exclusion ◽  
Low Molecular Weight ◽  
Exclusion Chromatography ◽  
Liver And Kidney

SummaryIt is widely reported that persistent anti-Xa activity follows administration of low molecular weight heparins. To identify the effectors of this activity we have injected 125I-labelled Enoxaparin sodium into rabbits and subsequently analysed the circulating radiolabelled material and anti-Xa activity by affinity and size exclusion chromatography. Antithrombin III-binding material derived from the injected drug was responsible for all the anti-Xa amidolytic activity. At early times after injection additional anticoagulant activity which was largely attributable to tissue factor pathway inhibitor was measured by the Heptest clotting assay after removal of glycosaminoglycans from plasma samples. Small radiolabelled fragments, including penta/hexasaccharide with affinity for antithrombin III, were detectable in the circulation 1 week later, and sulphated oligosaccharides persisted for 3-4 weeks. Significant quantities of radiolabel remained in the liver and kidney several weeks post-injection; these organs may sequester some of the injected drug and give rise to circulating biologically active material by degradation and secretion of catabolic products into the plasma.

A study on the kinetics and thermal properties of polystyrene/diatomite nanocomposites prepared via in situ ATRP

2018 ◽  
Vol 33 (2) ◽  
pp. 180-197 ◽  
Author(s):  
Khezrollah Khezri ◽  
Yousef Fazli
Keyword(s):  
Molecular Weight ◽  
In Situ Polymerization ◽  
Structural Characteristics ◽  
Nitrogen Adsorption ◽  
Linear Increase ◽  
Size Exclusion ◽  
Scanning Calorimetry ◽  
Morphological Studies ◽  
Exclusion Chromatography

Pristine mesoporous diatomite was employed to prepare polystyrene/diatomite composites. Diatomite platelets were used for in situ polymerization of styrene by atom transfer radical polymerization to synthesize tailor-made polystyrene nanocomposites. X-Ray fluorescence spectrometer analysis and thermogravimetric analysis (TGA) were employed for evaluating some inherent properties of pristine diatomite platelets. Nitrogen adsorption/desorption isotherm is applied to examine surface area and structural characteristics of the diatomite platelets. Evaluation of pore size distribution and morphological studies were also performed by scanning and transmission electron microscopy. Conversion and molecular weight determinations were carried out using gas and size exclusion chromatography, respectively. Linear increase of ln ( M0/M) with time for all the samples shows that polymerization proceeds in a living manner. Addition of 3 wt% pristine mesoporous diatomite leads to an increase of conversion from 72% to 89%. Molecular weight of polystyrene chains increases from 11,326 g mol−1 to 14134 g mol−1 with the addition of 3 wt% pristine mesoporous diatomite; however, polydispersity index values increases from 1.13 to 1.38. Increasing thermal stability of the nanocomposites is demonstrated by TGA. Differential scanning calorimetry shows an increase in glass transition temperature from 81.9°C to 87.1°C by adding 3 wt% of mesoporous diatomite platelets.

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