Effects of Raw Material Source on the Properties of CMC Composite Films

Sodium carboxymethyl cellulose (CMC) can be derived from a variety of cellulosic materials and is widely used in petroleum mining, construction, paper making, and packaging. CMCs can be derived from many sources with the final properties reflecting the characteristics of the original lignocellulosic matrix as well as the subsequent separation steps that affect the degree of carboxy methyl substitution on the cellulose hydroxyls. While a large percentage of CMCs is derived from wood pulp, many other plant sources may produce more attractive properties for specific applications. The effects of five plant sources on the resulting properties of CMC and CMC/sodium alginate/glycerol composite films were studied. The degree of substitution and resulting tensile strength in leaf-derived CMC was from 0.87 to 0.89 and from 15.81 to 16.35 MPa, respectively, while the degree of substitution and resulting tensile strength in wooden materials-derived CMC were from 1.08 to 1.17 and from 26.08 to 28.97 MPa, respectively. Thus, the degree of substitution and resulting tensile strength tended to be 20% lower in leaf-derived CMCs compared to those prepared from wood or bamboo. Microstructures of bamboo cellulose, bamboo CMC powder, and bamboo leaf CMC composites’ films all differed from pine-derived material, but plant source had no noticeable effect on the X-ray diffraction characteristics, Fourier transform infrared spectroscopy spectra, or pyrolysis properties of CMC or composites films. The results highlighted the potential for using plant source as a tool for varying CMC properties for specific applications.

Self-Assembly of Soluble Chitosan Derivatives Nanoparticles for Vaccine: Synthesis, Characterization and Evaluation

Herein, a novel chitosan derivative nanoparticle was proposed to function as a delivery carrier. First of all, an improvement was made to the way N-2-hydroxypropyl trimcthyl ammonium chloride chitosan (N-2-HACC) was synthesized. Moreover, the solution to one-step synthesis of N-2-HACC from chitosan (CS) was developed. Different from the previous report, the synthesis process was simplified, and there was a reduction in the amount of 2,3-epoxypropyl trimethyl ammonium chloride (EPTAC) used. With its excellent water solubility maintained, the relatively low degree of substitution was controlled to facilitate the cross-linking reaction. The results obtained from 1H-NMR, FTIR spectroscopy, and XRD indicated a smooth EPTAC onto CS for the formation of N-2-HACC with 59.33% the degree of substitution (DS). According to our results, N-2-HACC could be dissolved in various organic solvents, deionized water, 1% acetic acid aqueous solution, and others at room temperature. Finally, a novel chitosan nanoparticle material was prepared using the self-assembly method with β-glycerophosphate sodium (β-GC), with excellent immune properties achieved, thus providing a new strategy for chitosan self-assembled nanoparticles.

Cellulose acetate obtained from Schizolobium parahyba (vell.) blake wood

Currently, non-biodegradable polymers are produced on a large scale and cause several environmental problems, especially due to their low degradation. Cellulose acetate is a non-toxic, low-flammable and low-cost polymer, playing an important environmental role. The objective of this study was to synthesize cellulose acetate membranes from Schizolobium parahyba wood (“guapuruvu”) with particles sizes of 20 and 60 mesh. The materials were submitted to acetosolv pulping, bleaching and acetylation to produce the acetates. The yields and the degree of substitution were found. The fibers were chemically characterized and the samples obtained at each processing step were analyzed by FTIR. It was possible to prepare acetates from both granulometries wood. The FTIR analysis showed changes on the samples’ bands, indicating that the chemical processes were efficient. Cellulose acetate obtained from the 60 mesh material presented a higher degree of substitution (2.74 ± 0.12) when compared to the 20 mesh acetate (2.59 ± 0.13), showing that the particle size of the material influenced on the efficiency of the acetylation reaction. DMA tests have demonstrated that the 60 mesh membrane has higher flexibility and transparency when compared to the 20 mesh membrane.

Esterification of cellulose with betaine using p-toluenesulfonyl chloride for the in-situ activation of betaine

A novel synthesis method was developed for betaine-modified cellulose ester using a mixed N,N-dimethylacetamide/lithium chloride solvent system; p-toluenesulfonyl chloride was used for the in-situ activation of the betaine. The influence of the reaction temperature and time, as well as the anhydroglucose unit to p-toluenesulfonyl chloride to betaine mass ratio on the degree of substitution of the product was evaluated. Increasing the proportion of betaine and p-toluenesulfonyl chloride was beneficial to the esterification reaction. The degree of substitution was 1.68 at 90 °C for 32 h with an anhydroglucose unit to p-toluenesulfonyl chloride to betaine molar ratio of 1 to 2 to 3. The physicochemical properties of the betaine-modified cellulose were closely related to the degree of substitution. Major changes in the morphologies, crystallinity, thermal properties, porosity, and the average degree of polymerization resulted from the modification. The introduction of betaine made cellulose esters thermally less stable than neat cellulose but more difficult to completely degrade. The crystalline structure of the cellulose esters was destroyed, and the products exhibited a porous nature. Dye sorption studies demonstrated that the betaine-modified cellulose holds the potential of adsorbing anionic substances, which is the premise of its application.

Effect of Molecular Weight and Degree of Substitution on the Physical-Chemical Properties of Methylcellulose-Starch Nanocrystal Nanocomposite Films

This research studied the effect of molecular weight (Mw) and degree of substitution (DS) on the microstructure and physicochemical characteristics of methylcellulose (MC) films with or without SNC. The Mw and DS of three types of commercial MC (trade name of M20, A4C, and A4M, respectively) were in the range of 0.826 to 3.404 × 105 Da and 1.70 to 1.83, respectively. Mw significantly affected the viscosity of methylcellulose solutions as well as the microstructure and tensile strength of methylcellulose films, while DS had a pronounced effect on their oxygen permeability properties. The incorporation of 15% (w/w) SNC resulted in the efficient improvement of tensile strength, water, and oxygen barrier properties of films, particularly for the A4C nanocomposite films. The results from SEM and FTIR illustrated that relatively homogenous dispersion of SNC was distinguished in A4C-15% (w/w) SNC films. Furthermore, microstructures of MC-SNC nanocomposite films were strongly dependent on both Mw and DS of MC. This work offers a convenient and green method to fabricate MC-based nanocomposite films with desirable mechanical, light, oxygen, and water vapor barrier properties.