Behavior of xylans from the Eucalyptus species. Part 2. Characterization of 4-O-methylglucuronoxylans isolated from black liquors of kraft pulping of Eucalyptus grandis and E. urophylla

Holzforschung ◽  
2013 ◽  
Vol 67 (2) ◽  
pp. 123-128
Author(s):  
Andréia S. Magaton ◽  
Teresa Cristina F. Silva ◽  
Jorge Luiz Colodette ◽  
Dorila Piló-Veloso ◽  
Flaviana Reis Milagres ◽  
...  

Abstract 4-O-methylglucuronoxylans isolated from Eucalyptus grandis and Eucalyptus urophylla kraft black liquors (KBLs) were chemically characterized by Fourier transform infrared spectroscopy (FT-IR), size exclusion chromatography (SEC), and nuclear magnetic resonance (NMR) spectroscopy. Doses of alkali charge, expressed as active alkali (AA), were 16, 17, and 18% while the sulfidity was kept at 25%. Kappa numbers of 19.1, 17.5, and 16.1 for E. grandis and 20.4, 16.8, and 15.4 for E. urophylla were obtained. At higher alkali charges, the recovery of xylans from the KBLs was lower and the degree of substitution of xylans with uronic acids decreased. The average molecular weight (Mw) of the recovered xylans was greater under conditions of mild pulping, i.e., in the case of pulps with higher kappa numbers. Mw of xylans ranged from 16.1 to 19.1 kDa for E. grandis and from 15.4 to 20.4 kDa for E. urophylla. The xylans from KBL may be useful as pulp modifying agents or as a raw material for advanced applications.

Holzforschung ◽  
2013 ◽  
Vol 67 (2) ◽  
pp. 115-122 ◽  
Author(s):  
Andréia S. Magaton ◽  
Teresa Cristina F. Silva ◽  
Jorge Luiz Colodette ◽  
Dorila Piló-Veloso ◽  
Flaviana Reis Milagres

Abstract 4-O-methylglucuronoxylans were isolated from the wood and pulp of different Eucalyptus species (E. dunni, E. grandis, E. nitens, E. urograndis and E. urophylla) and characterized by 1H NMR spectroscopy and size-exclusion chromatography (SEC). The content of 4-O-methylglucuronic acid (MeGlcA) varied between the eucalyptus species from 1.90 to 2.80 expressed as MeGlcA/10 xyloses, whereas in the pulp, the total uronic acid content was approximately 1.02, from which the half was hexenuronic acid (HexA). From the MeGlcA linked to the xylan chain 9–26% are substituted in position O-2 by hexose units. The Mw of the xylans extracted from wood ranged between 26.1 and 28.4 kDa. The retention of 4-O-methylglucuronoxylans (51.3–58.7%) during kraft pulping was high, and the retention is related to the content of MeGlcA group, the content of MeGlcA group substituted at O-2, and the average molecular weight of the xylans. The parameters observed affect the overall pulp yield and pulp properties.


Holzforschung ◽  
2008 ◽  
Vol 62 (1) ◽  
pp. 24-30 ◽  
Author(s):  
Anderson Guerra ◽  
Lucian A. Lucia ◽  
Dimitris S. Argyropoulos

Abstract Despite the growing importance of Eucalyptus wood as raw material for pulp and paper, there is a lack of knowledge on the chemistry of their macromolecular components. The present paper addresses this issue by applying the recently developed protocol for isolating enzymatic mild acidolysis lignins (EMAL) from Eucalyptus grandis, Eucalyptus globulus and the softwood species Douglas fir and white fir, which were used for comparative purposes. The structures of EMALs were investigated by quantitative 31P NMR, DFRC/31P NMR (derivatization followed by reductive cleavage followed by quantitative 31P NMR) and size exclusion chromatography (SEC). Overall, the yields of EMALs isolated from Eucalyptus were higher than those from the softwoods examined. Lignin from E. globulus was found to contain higher contents of arylglycerol-β-aryl ether structures, free phenolic hydroxyl groups and syringyl-type units than lignin from E. grandis. New insights provided by the DFRC/31P NMR revealed that up to 62.2% of arylglycerol-β-aryl ether structures in E. globulus are uncondensed, while in E. grandis the amount of such uncondensed structures was found to be lower than 48%. SEC analyses showed that lignins from E. grandis and softwoods associate in greater extension than lignin from E. globulus.


e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Jerzy Chruściel ◽  
Marzena Fejdyś ◽  
Zofia Michalska ◽  
Witold Fortuniak

AbstractTwelve new liquid branched poly(methylhydrosiloxanes) of random structures (b-r-PMHS), containing triple branching units MeSiO1.5 (T), both Me2SiO (D) and MeHSiO (DH) chain building units (or only mers MeHSiO), and terminal groups Me3SiO0.5, have been prepared by hydrolytic polycondensation method of appropriate organic chlorosilanes in diethyl ether medium at temperatures < 0 °C. Two b-r-PMHS containing structural units: M, D, DH, T and TH have been obtained as well. Volatile low molecular weight oligosiloxanes were removed by vacuum distillation at 125-150 °C. Yields of b-r-PMHS ranged from 57 to 84 wt. %. All polymeric products were characterized by FT-IR, 1H- and 29Si-NMR, and elemental analysis. Their dynamic viscosities were determined in the Brookfield HBDV+IIcP cone-plate viscometer. The molecular weights of b-r-PMHS and polydispersities of MW were analyzed by size exclusion chromatography (SEC).


Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1993
Author(s):  
Sebastián Bonardd ◽  
Alejandro Ángel ◽  
Ángel Norambuena ◽  
Deysma Coll ◽  
Alain Tundidor-Camba ◽  
...  

The following work shows, for the first time, the synthesis and characterization of a new family of polyelectrolytes, along with their preliminary assessments in terms of desalin water treatment. These materials fall into the category of aromatic co-polyamides, which are obtained by the direct condensation of monomers 4,4′-oxydianiline (ODA), isophthaloyl chloride, and 3,5-diamino-N-(pyridin-4-ylmethyl)benzamide (PyMDA). Thereby, the charged nature exhibited by these materials was achieved through the quaternization of PyMDA moieties using linear iodoalkanes of different lengths (CnI with n = 1, 2, 4, and 6). After completing the quaternization process, polyelectrolytes were subjected to a one-step anion substitution process, where iodide counterions were replaced by bis(trifluoromethane)sulfonamide entities. For all the obtained materials, solubility tests were carried out, showing that those alkylated with methyl and ethyl chains exhibit high solubility in rutinary aprotic polar solvents, while those containing n-butyl and n-hexyl units resulted in the formation of insoluble gels. Due to the above, the latest were discarded from this study early on. The structural characterization of the initial neutral co-polyamide was carried out by means of infrared spectroscopy (FT-IR), nuclear magnetic resonance (1H, 13C-NMR), and size-exclusion chromatography (SEC), while the structure of methylated and ethylated polyelectrolytes was successfully confirmed through FT-IR, 1H, 13C, and 19F-NMR. Additionally, the thermal behavior of these materials was analyzed in terms of thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), showing thermal degradation temperatures above 300 °C and glass transition temperatures (Tg) above 200 °C, resulting in polymers with outstanding thermal properties for water treatment applications. On the other hand, through the solvent-casting method, both neutral and charged polymers were found to be easily prepared into films, exhibiting a remarkably flexibility. The mechanical properties of the films were analyzed using the traction test, from which tensile strength values ranging between 83.5 and 87.9 Mpa, along with Young’s modulus values between 2.4 and 2.5 Gpa were obtained. Moreover, through contact angle measurements and absorption analysis by immersion, polyelectrolytes showed important changes in terms of affinity against polar and polar substances (water, n-heptane, and benzene), exhibiting a higher rejection regarding the neutral polymer. Finally, as a preliminary test against the seepage of saline waters, thin polymer films (from 11.4 to 17.1 µm) were deposited on top of commercial filter discs and tested as filters of saline solutions ([NaCl] = 1000 and 2000 ppm). These tests revealed a decrease of the salt concentration in the obtained filtrates, with retention values ranging between 6.2 and 20.3%, depending on the concentration of the former solution and the polymer used.


2021 ◽  
Author(s):  
Santiago Pablo Fernandez Bordin ◽  
Juan Manuel Padró ◽  
Víctor Galván Josa ◽  
Marcelo Ricardo Romero

In past decades, the combination of polymers to obtain blends in film shapes has been a very effective strategy to meet the needs of the increasingly demanding market. In this sense, pH- and thermo-sensitive (PHT) polymers have recently drawn the attention of researchers for their countless applications. However, binary mixtures of typical PHTs like polyacrylic acid (p-AAc) and poly-N-isopropylacrylamide (p-NIPAm) were unable to form films. In this sense, it was hypothesized that NIPAm copolymerized with AAc monomers can yield blends with virtually the same functional group composition of binary mixtures of p-NIPAm and p-AAc homopolymers but with different properties of film formation. For this, a copolymeric radical synthesis and the subsequent analytical studies were complemented to get a broad description of these materials. P-NIPAm and p-AAc homopolymers and different proportions of copolymers p-NIPAm-co-AAc were obtained and thoroughly characterized by Fourier Transform Infrared Spectroscopy (FT-IR), Size Exclusion Chromatography (SEC), acid-basic titration, and rotational rheology. Among the samples, the solutions of p-AAc with p-NIPAm and p-NIPAm-co-AAc copolymers with a higher proportion of NIPAm units (0.8 and 0.6 NIPAm/AAc) precipitated as interpolymer complexes. Since it was expected, the combination with p-NIPAm-co-AAc 40/60 copolymer, which has a higher proportion of AAc groups and pH sensitivity, allowed obtaining blends suitable for the preparation of films. Furthermore, despite the fact that the combinations of p-NIPAm-co-AAc 40/60 with p-NIPAm-co-AAc 80/20 or p-NIPAm were successful, the mechanical properties of the films are worse compared to the other blends, leaving this issue open for subsequent studies.


2020 ◽  
Author(s):  
M Wee ◽  
M Mastrangelo ◽  
Susan Carnachan ◽  
Ian Sims ◽  
K Goh

A shear-thickening water-soluble polysaccharide was purified from mucilage extracted from the fronds of the New Zealand black tree fern (Cyathea medullaris or 'mamaku' in Māori) and its structure characterised. Constituent sugar analysis by three complementary methods, combined with linkage analysis (of carboxyl reduced samples) and 1H and 13C nuclear magnetic resonance spectroscopy (NMR) revealed a glucuronomannan comprising a backbone of 4-linked methylesterified glucopyranosyl uronic acid and 2-linked mannopyranosyl residues, branched at O-3 of 45% and at both O-3 and O-4 of 53% of the mannopyranosyl residues with side chains likely comprising terminal xylopyranosyl, terminal galactopyranosyl, non-methylesterified terminal glucopyranosyl uronic acid and 3-linked glucopyranosyl uronic acid residues. The weight-average molecular weight of the purified polysaccharide was ~1.9×106Da as determined by size-exclusion chromatography coupled with multi-angle laser light scattering (SEC-MALLS). The distinctive rheological properties of this polysaccharide are discussed in relation to its structure. © 2014 Elsevier B.V.


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