Thermal and mechanical properties of chitosan nanocomposites with cellulose modified in ionic liquids

In this paper, ionic liquid treatment was applied to produce nanometric cellulose particles of two polymorphic forms. A complex characterization of nanofillers including wide-angle X-ray scattering, Fourier transform infrared spectroscopy, and particle size determination was performed. The evaluated ionic liquid treatment was effective in terms of nanocrystalline cellulose production, leaving chemical and supermolecular structure of the materials intact. However, nanocrystalline cellulose II was found to be more prone to ionic liquid hydrolysis leading to formation larger amount of small particles. Each nanocrystalline cellulose was subsequently mixed with a solution of chitosan, so that composite films containing 1, 3, and 5% mass/mass of nanometric filler were obtained. Reference samples of chitosan and chitosan with micrometric celluloses were also solvent casted. Thermal, mechanical, and morphological properties of films were tested and correlated with properties of filler used. The results of both, tensile tests and thermogravimetric analysis showed a significant discrepancy between composites filled with nanocrystalline cellulose I and nanocrystalline cellulose II.     

Discoloration of celluloses treated with amino compounds

Degradation and discoloration of celluloses treated with different amino compounds, including primary amines and hexamethylenetetramine (HMTA), were studied using spectroscopic techniques. The colour generation was measured using standard colorimetry and the degradation and discoloration were characterized using diffuse reflectance FTIR spectroscopy and diffuse reflectance UV-visible spectroscopy. The colour of all the treated celluloses was due to the same chromophores, thus revealing that the discoloration mechanism was essentially the same. The most important reaction was the condensation between carbonyl and amino groups to form coloured imines, and secondary processes were detected at high temperatures and long heating times. The discoloration of celluloses modified with primary amines followed first-order kinetics. However, the discoloration of HMTA-treated cellulose showed an induction period which was related to the thermal decomposition of HMTA.     

Photooxidation of cellulose treated with amino compounds

The effect of short wavelength UV radiation on celluloses treated with different amino compounds was studied. Samples of cotton cellulose were treated in aqueous solutions of different pH with polyethylenimine (PEI), hexamethylenetetramine (HMTA) and ethylenediamine (EDA), and irradiated in air with a low pressure mercury vapour lamp for different times. The photoyellowing was measured using standard colorimetry and the degradation processes and products were characterized using diffuse reflectance (FTIR and UV-visible) spectroscopy. The degradation processes were compared with those observed in the same materials during thermal treatments. Celluloses treated with EDA and PEI show an intense photoyellowing which depends on the pH of the treating solution. Colour changes in these materials correlate well with the appearance of imine groups and the disappearance of amino groups, determined by FTIR measurements. However, HMTA-treated cellulose, which suffers an intense thermal yellowing, shows only insignificant photoyellowing. These results were explained considering that the photoyellowing is due to the coloured Schiff bases produced in the condensation between amino and carbonyl groups.     

Degrees of polymerization (DP) and DP distribution of dilute acid-hydrolyzed products of alkali-treated native and regenerated celluloses

Three groups of cellulose II samples, 20% NaOH-treated native celluloses (M-native celluloses), commercial regenerated celluloses and those treated with 20% NaOH (M-regenerated celluloses), were subjected to dilute acid hydrolysis at 105 °C to obtain so-called leveling-off degrees of polymerization (LODP). Molecular mass parameters of the acid-hydrolyzed products were analyzed by SEC-MALLS using 1% LiCl/DMAc as an eluent. The LODP values were in the order of M-native celluloses ≅ M-regenerated celluloses > regenerated celluloses. The LODP values of M-regenerated celluloses are 1.5–1.7 times as much as those of the regenerated celluloses; the cellulose II crystallites in regenerated celluloses increase in size to the longitudinal direction by the alkali treatment and the successive acid hydrolysis at 105 °C. This increase in the longitudinal crystal sizes might primarily occur during acid hydrolysis. All the acid-hydrolyzed products had bimodal SEC elution patterns, i.e. the predominant high-molecular-mass and minor low-molecular-mass components, the latter of which corresponded to DP 20.     

Thermal compatibility studies of nitroimidazoles and excipients

Nitroimidazoles are heterocycle imidazoles with a nitrogen group incorporated in its structure. The objective of this study was to develop a model to characterize possible interactions between active substances and excipients using: Thermogravimetry, Differential Thermal Analysis, Differential Scanning Calorimetry, and DSC coupled to photovisual system. It was used three nitroimidazoles (metronidazole, secnidazole, and tinidazole) and two types of microcrystalline cellulose with different particle size (Microcel and Avicel). The binary mixtures were prepared in proportion (w/w) 1:1 (nitroimidazole:excipient). Thermogravimetric data demonstrated that the tinidazole was the nitroimidazole with better uniformity. The nitroimidazoles obeyed the zero order kinetic reaction, evidencing its vaporization processes. Differential thermal analysis data showed nitroimidazoles compatibility with the different microcrystalline celluloses studied, showing that microcrystalline celluloses stabilized the active substances. Calorimetric data of secnidazole showed two melting points, characteristic of the polymorphs presented in raw material. The vaporization constants values of nitroimidazoles studied were secnidazole > metronidazole > tinidazole and for the binary mixtures these values followed the order tinidazole > metronidazole ≥ secnidazole.     

Binding cellulose and chitosan via click chemistry: Synthesis,characterization, and formation of some hollow tubes

A novel cellulose‐click‐chitosan polymer was prepared successfully in three steps: (1) propargyl cellulose with degrees of substitution (DS) from 0.25 to 1.24 was synthesized by etherification of bamboo Phyllostachys bambusoide cellulose with propargyl chloride in DMA/LiCl in the presence of NaH. The regioselectivity of propargylation on anhydrous glucose unit determined by GC‐MS was in the order of 2 >> 6 > 3; (2) the functional azide groups were introduced onto the chitosan chains by reacting chitosan with 4‐azidobenzoic acid in [Amim]Cl/DMF and the DS ranged from 0.02 to 0.46; (3) thus, the cellulose‐click‐chitosan polymer was obtained via click reaction, that is, the Cu(I)‐catalyzed Huisgen 1,3‐dipolar cycloaddition reaction, between the terminal alkyne groups of cellulose and the azide groups on the chitosan backbone at room temperature. The successful binding of cellulose and chitosan was confirmed and characterized by FTIR and CP/MAS ¹³C NMR spectroscopy. TGA analyses indicated that the cellulose‐click‐chitosan polymer had a higher thermal stability than that of cellulose and chitosan as well as cellulose–chitosan complex. More interestingly, some hollow tubes with near millimeter length were also observed by SEM. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Silylated Cellulose Materials in Design of Supramolecular Structures of Ultrathin Cellulose Films

Abstract

To use the structure-forming potential and the biodegradability of cellulose and nonionic cellulose ethers, we developed synthesis pathways for soluble and regenerable silyl celluloses suitable for the design of advanced materials. A 6-0-silylation of cellulose takes place in a heterogeneous phase reaction in the presence of ammonia-saturated polar aprotic solvents at ?15°C with thexyldimethylchlorosilane. After 2,3-di-O-methylation, this type of regioselectively-substituted cellulose derivatives yields sensor matrices for the detection of halohydrocarbons in air. On the other hand, thexyldimethylsilyl celluloses and trimethylsilyl celluloses with degrees of substitution in the 2.6 to 3.0 range form mono-and multilayered supramolecular structures by applying the Langmuir–Blodgett technique and, after desilylation, oriented ultrathin cellulose films.     

Simple functionalization of cellulose beads with pre-propargylated chitosan for clickable scaffold substrates

Concerning the increased market for bio-based materials and environmentally safe practices, cellulose-based beads are one of the more attractive alternatives. Thus, this work focuses on the generation of functional cellulose-based beads with a relatively simple and direct method of blending a pre-modified chitosan bearing the targeted functional groups and cellulose, prior to the formation of the beads, as a mean to have functional groups in the formed structure. To this end, chitosan was chemically modified with propargyl bromide in homogenous reaction conditions and then combined with cellulose in sodium hydroxide/urea solution and coagulated in nitric acid to produce spherical shaped beads. The successful chemical modification of chitosan was assessed by elemental analysis, as well as by Fourier-transform infrared spectroscopy, Raman spectroscopy and X-ray photoelectron spectroscopy. The alkynyl moieties from the chitosan derivative, served as reactive functional groups for click-chemistry as demonstrated by the tagging of the commercial fluorophore Azide-Fluor 488 via CuI-catalysed alkyne-azide cycloaddition reaction, in aqueous media. This work demonstrates the one-step processing of multiple polysaccharides for functional spherical beads as a template for bio-based scaffolds such as enzyme immobilization for stimuli-response applications and bioconjugations.

     

13C CPMAS NMR investigations of cellulose polymorphs in different pulps

In order to obtain information about the crystallinity and polymorphs of cellulose, and the occurrence of hemicelluloses in pulp fibers, wood cellulose, bacterial cellulose, cotton linters, viscose, and celluloses in different pulps were investigated by solid state ¹³C CPMAS NMR spectroscopy. A mixed softwood kraft pulp and a dissolving-grade pulp were treated under strongly alkaline and acidic conditions and the effect on cellulose crystallinity was studied. The presence of different crystalline polymorphs of cellulose and the amounts of hemicelluloses are considered.     

Trichoderma reesei cellulases and their core domains in the hydrolysis and modification of chemical pulp

The action of monocomponent Trichoderma reesei endoglucanases (EG I, EG II; EC 3.2.1.4) and cellobiohydrolases (CBH I, CBH II; EC 3.2.1.91) and their core proteins was compared using isolated celluloses and bleached chemical pulp. The presence of cellulose binding domain (CBD) in the intact enzymes did not affect their action against soluble substrates. In the case of insoluble isolated celluloses and the chemical pulp the presence of CBD enhanced the enzymatic hydrolysis of cellulose. The effect of CBD was more pronounced in the cellobiohydrolases, hydrolysing mainly crystalline cellulose, than in the endoglucanases which were more efficient in hydrolysing amorphous cellulose. The pulp properties measured, that is, viscosity and strength after PFI refining, were equally affected by the treatment with intact enzymes and corresponding core proteins, suggesting that the presence of CBD in intact cellulases affects mainly the cellulose hydrolysis level and less the mode of action of T. reesei cellulases in pulp. The better beatability of the bleached chemical pulp treated with intact endoglucanases than that treated with the corresponding core proteins suggests that the presence of CBD in endoglucanases could, however, result in beneficial effects on pulp properties.     

Preparation of photoinitiator-bound celluloses and their reactivity

Photoinitiator-bound celluloses (Cell-AQ and Cell-BP) were prepared by reaction of epoxy-activated cellulose with, respectively, 1-aminoanthraquinone (AQNH₂) and 4-aminobenzophenone (BPNH₂) in N,N-dimethylformamide at 70°C. About 60% of the initial epoxy groups (1·90–2·10 mmol/(g cellulose)) was found to participate in the reaction under alkaline conditions. The photoinitiator-bound celluloses exhibited an activity towards photoinduced formation of hydrogen peroxide in aqueous solutions of -glucose, and isopropyl alcohol. The amount of hydrogen peroxide formed was higher for the Cell-BP than the Cell-AQ. Moreover, the photoinitiator-bound celluloses showed an ability to initiate photografting of methyl methacrylate at 60°C in a water medium, indicating a higher percentage of grafting and a lower percentage of homopolymer compared to photoinitiator-sensitized celluloses, which were prepared by immersing a cellulose sample in acetone solutions of AQNH₂ and BPNH₂ and drying under vacuum to remove the solvent. It was found that the photoinitiator residues introduced into the cellulose substrate are capable of abstracting hydrogen atoms from the substrate.     

秸秆纤维素的一步快速提取和水解

研究了秸秆纤维素的一步快速提取方法, 在醋酸和硝酸溶液体系中, 选择10种不同的反应条件, 进行了提取条件优选, 然后对提取的纤维素样品分别进行了水解. 结果发现, 纤维素提取的最佳条件为120 ℃, 固液比为1∶25, 在体积分数为80%的醋酸和10%的硝酸混合溶液中反应20 min, 纤维素的产率为38%. 纤维素样品的水解实验发现, 在最佳条件下提取样品的葡萄糖含量都大于90%, 水解率达到94%. 13C NMR和FTIR分析结果表明, 纤维素的分子结构未被破坏, 但纤维素Ⅰβ含量较高, 木质素和半纤维素的去除率都很高, 表明此方法是比较理想的制备高纯度纤维素的方法.     

Oxidation and structural changes in NMMO-regenerated cellulose films

Carbonyl and carboxyl groups introduced by oxidative processes during production and purification of celluloses determine intra- and intermolecular interactions and thus application-related bulk and surface properties of cellulosic materials. We report a comprehensive approach to the quantification of carboxyl and carbonyl groups in cellulose films upon reconstitution from NMMO solutions. Measurements of the excess conductivity were combined with the determination of the molecular weight distribution, quantification of the carboxyl and carbonyl group content, crystallinity and film swelling in aqueous solutions. TEMPO-oxidized, NMMO-regenerated cellulose films were additionally analysed as a reference system for extensive cellulose oxidation. Our reported data demonstrate that dissolution of cellulose in NMMO results in the formation of onic acids, chain degradation, increased ionization and film swelling, whereas TEMPO-oxidation introduced carbonyl groups as well as onic and uronic acids causing a significantly increased charging, ion accumulation and swelling even at higher crystallinity.     

Effect of cellulase adsorption on the surface and interfacial properties of cellulose

The surface properties of several purified cellulose (Sigmacell 101, Sigmacell 20, Avicel pH 101, and Whatman CF 11) were characterised, before and after cellulase adsorption. The following techniques were used: thin-layer wicking (except for the cellulose Whatman), thermogravimetry, and differential scanning calorimetry (for all of the above celluloses). The results obtained from the calorimetric assays were consistent with those obtained from thin-layer wicking – Sigmacell 101, a more amorphous cellulose, was the least hydrophobic of the analysed celluloses, and had the highest specific heat of dehydration. The other celluloses showed less affinity for water molecules, as assessed by the two independent techniques. The adsorption of protein did not affect the amount of water adsorbed by Sigmacell 101. However, this water was more strongly adsorbed, since it had a higher specific heat of dehydration. The more crystalline celluloses adsorbed a greater amount of water, which was also more strongly bound after the treatment with cellulases. This effect was more significant for Whatman CF-11. Also, the more crystalline celluloses became slightly hydrophilic, following protein adsorption, as assessed by thin-layer wicking. However, this technique is not reliable when used with cellulase treated celluloses.     

Degrees of polymerization (DP) and DP distribution of cellouronic acids prepared from alkali-treated celluloses and ball-milled native celluloses by TEMPO-mediated oxidation

Various cellulose II samples, ball-milled native celluloses and ball-milled wood saw dust were subjected to 2,2,6,6-tetramethypyperidine-1-oxyl radical (TEMPO)-mediated oxidation to prepare cellouronic acid Na salts (CUAs). The TEMPO-oxidized products obtained were analyzed by ¹³C-NMR and size-exclusion chromatography (SEC). When the cellulose II samples with degrees of polymerization (DP) of 220–680 were used as the starting materials, the CUAs obtained had weight-average DP (DPw) values of only 38–79. Thus, significant depolymerization occurs on cellulose chains during the TEMPO-mediated oxidation. These DP values of CUAs correspond to the cellulose II crystal sizes along the chain direction in the original cellulose II samples, but not necessarily to their leveling-off DP values. CUAs can be obtained also from ball-milled native celluloses in good yields by TEMPO-mediated oxidation, although their DPw values are lower than about 80. On the other hand, CUA with DPw of about 170 was obtained from ball-milled wood saw dust.     

Cellulose II nanoelements prepared from fully mercerized, partially mercerized and regenerated celluloses by 4-acetamido-TEMPO/NaClO/NaClO2 oxidation

A softwood bleached kraft pulp (SBKP) and cotton lint cellulose were fully or partially mercerized, and these along with celluloses and commercially available regenerated cellulose fiber and beads were oxidized by 4-acetamido-TEMPO/NaClO/NaClO₂ at 60 °C and pH 4.8. Weight recovery ratios and carboxylate contents of the oxidized celluloses were 65–80% and 1.8–2.2 mmol g⁻¹, respectively. Transparent and viscous dispersions were obtained by mechanical disintegration of the TEMPO-oxidized celluloses in water. These aqueous dispersions showed birefringence between cross-polarizers, indicating that mostly individualized cellulose nanoelements dispersed in water were obtained by these procedures. Transmission electron microscopy observation showed that the cellulose nanoelements prepared from mercerized SBKP, repeatedly mercerized SBKP, mercerized cotton lint cellulose, regenerated cellulose beads and 18% NaOH-treated SBKP, i.e. partially mercerized SBKP, had similar morphologies and sizes, 4–12 nm in width and 100–200 nm in length. The 18% NaOH-treated SBKP was converted to cellulose nanoelements consisting of both celluloses I and II.     

Mechanical properties of films made from dialcohol cellulose prepared by homogeneous periodate oxidation

2,3-Dialdehyde celluloses were prepared by homogeneous periodate oxidation in an aqueous solution of methylol cellulose. Since methylol cellulose stays dissolved in water for a certain time before decomposing gradually into regenerated cellulose, the oxidation reaction progressed homogeneously throughout the period. The resulting dialdehyde cellulose achieved an oxidation level of over 90 % in as little as 12 h. Reducing the dialdehyde celluloses with NaBH₄ resulted in water-soluble dialcohol celluloses, which have an open-ring structure at the C2–C3 position. The dialcohol celluloses were characterized using nuclear magnetic resonance spectrometry, Fourier transform infrared spectroscopy, and differential scanning calorimetry. The T_g of the products decreased with increasing oxidation levels. The products might be processable, and unique tensile properties were obtained by cutting the C2–C3 bonds in the glucopyranose rings. The dialcohol celluloses prepared using a cast method yielded clear and transparent films which showed unique mechanical properties by tensile tests depending on the values of oxidation level.     

Preparation,characterization, and properties of fast‐responding bulk hydrogel and treated bleached banana pulp

The reaction between bleached banana pulp and pure maleic anhydride (MA) was investigated. The reaction was conducted in a reactor in the presence of xylene used as a solvent and sodium hypophosphite as catalyst. The appearance of infrared absorption bands at 1891 and 1708 cm^?1 indicated that MA chemically reacted by esterification with bleached banana pulp. However, evidence of an esterification reaction was obtained between cellulose and MA. The production of fast‐responding bulk hydrogel with a high swelling ratio was also investigated. This hydrogel was synthesized first by the formation of maleated acrylamide particles and then by the graft copolymerization of the particles with cellulose. The maleated acrylamide particles were characterized with mass spectroscopy, and the formed hydrogl was characterized by FT‐IR. The esterification reaction between bleached banana pulp and maleated acrylamide was also studied. Steam absorption for bulk hydrogel, maleated acrylamide‐treated bleached banana pulp, MA‐treated cellulose and bleached banana pulp is higher than the steam absorption for untreated cellulose and bleached banana pulp. Compared with treated bleached banana pulp and cellulose, the hydrogel had very high swelling ratios and much faster swelling rates attributed to the collaboration of the ionized particles and bulk hydrogel. The number of ionic maleated acrylamide groups in the hydrogel affected the swelling behavior. Copyright © 2004 John Wiley & Sons, Ltd.     

Preparation of Polyuronic Acid from Cellulose by TEMPO-mediated Oxidation

Various cellulose samples were oxidized by 2,2,6,6,-tetramethylpipelidine-1-oxyl radical (TEMPO)-NaBr-NaClO systems, and the effects of oxidation conditions on chemical structures and degrees of polymerization of the products obtained were studied. In the case of regenerated and mercerized celluloses, almost all C6 primary alcohol groups were selectively oxidized to carboxyl groups, and water-soluble polyglucuronic acid (cellouronic acid) sodium salts were obtained almost quantitatively; the degrees of polymerization were influenced greatly by the amount of TEMPO added, and the oxidation time and temperatures. Cellouronic acids prepared from mercerized linter and kraft pulps had size exclusion chromatograms with two separate peaks due to higher and lower molecular weight fractions. On the other hand, only small amounts of carboxyl groups were introduced into native cellulose samples. Since polyglucuronic acids prepared from cellulose by the TEMPO–NaBr– NaClO systems regularly consist of the glucuronic acid repeating unit, differing from the conventional water-soluble cellulose derivatives, they may open new fields of cellulose utilization.     

Heterogeneous modification of various celluloses with fatty acids

Heterogeneous modification of various types of cellulose (microcrystalline cellulose, cellulose whiskers and regenerated cellulose) was performed with long-chain fatty acids by an esterification reaction. The differences in reactivity between the celluloses were studied as well as the influences of the chain length and double bond content of the fatty acids. The success of the modification reaction and the structure of modified samples were studied with diverse characterization methods. Surface modification changed the thermal stability of cellulose by decreasing the degradation temperature but also made the pyrolysis curve two-stepped due to the double bonds in the fatty acid chain. It was observed that the nature of the fatty acid affected the degree of substitution (DS). The longer the fatty acid chain was, the lower was the DS. Fatty acids with increased double bond content gave decreased DS. Regenerated cellulose seemed to have the highest surface reactivity due to the distinct morphological structure, which also led to a much lower quantity of fatty acids attached to the structure than for other modified cellulose particles. The mixture of tall oil fatty acids behaved in the same manner as the commercial fatty acids, proving to be an excellent “green” choice for this kind of application.