Bernard Riedl

Mechanical and barrier properties of nanocrystalline cellulose reinforced chitosan based nanocomposite films

Nanocrystalline cellulose (NCC) reinforced chitosan-based biodegradable films were prepared by solution casting. The NCC content in the films was varied from 1 to 10% (dry wt. basis). It was found that the tensile strength (TS) of the nanocomposite films with 5% (w/w) NCC content was optimum with an improvement of 26% compared to the control chitosan films. Incorporation of NCC also significantly improved barrier properties. Water vapor permeability (WVP) of the chitosan/NCC films was decreased by 27% for the optimum 5% (w/w) NCC content. Swelling studies revealed a decrease in water uptake of the NCC-reinforced chitosan films. Analyses of thermal properties showed no significant effect of NCC whereas X-ray diffraction studies confirmed the appearance of crystalline peaks in the nanocomposite films. Surface morphology of the films was investigated by scanning electron microscopy and it was found that NCC was dispersed homogenously into chitosan matrix.

Nanocrystalline cellulose (NCC) reinforced alginate based biodegradable nanocomposite film.

Nanocrystalline cellulose (NCC) reinforced alginate-based nanocomposite film was prepared by solution casting. The NCC content in the matrix was varied from 1 to 8% ((w/w) % dry matrix). It was found that the nanocomposite reinforced with 5 wt% NCC content exhibits the highest tensile strength which was increased by 37% compared to the control. Incorporation of NCC also significantly improved water vapor permeability (WVP) of the nanocomposite showing a 31% decrease due to 5 wt% NCC loading. Molecular interactions between alginate and NCC were supported by Fourier Transform Infrared Spectroscopy. The X-ray diffraction studies also confirmed the appearance of crystalline peaks due to the presence of NCC inside the films. Thermal stability of alginate-based nanocomposite films was improved after incorporation of NCC.

Thermal degradation behavior of cellulose fibers partially esterified with some long chain organic acids

The thermal degradation behavior of cellulose fibers and some fibrous cellulose esters with partial degree of substitution has been studied by thermogravimetry analysis (TG) and differential scanning calorimetry (DSC). Cellulose esters were prepared by heterogeneous esterification in Py/TsCl with unsaturated or saturated long chain organic acids [undecylenic (C11), undecanoic (C11), oleic (C18) and stearic (C18)]. The thermal degradation of cellulose fibers follows a one-step process. The thermal stability of cellulose esters is inferior to that of unmodified cellulose fibers and the thermograms show a two-step degradation process, probably controlled by crosslinking reactions, which occur during thermal decomposition. Exothermic peaks in the DSC thermograms are also an indication of such reactions. Kinetic parameters such as the activation energy E, order of decomposition n, and frequency factor Z were obtained following the Friedman method. The cellulose sample followed first order of decomposition, however for cellulose esters higher orders were observed.

Comparative study of lignins isolated from Alfa grass (Stipa tenacissima L.)

Soda lignin, dioxane lignin and milled lignin were isolated from Alfa grass (Stipatenacissima L.). The physico-chemical characterization of three different lignins: one industrial lignin precipitated from soda spent liquor and two lignin preparations isolated under laboratory conditions from Alfa grass (also know as Esparto grass) was performed. The structures of lignins were studied by three non-destructive (FT-IR, solid state (13)C NMR and UV/visible spectroscopy) and two destructive (nitrobenzene oxidation and thermogravimetric analysis) methods. Elemental analysis and the methoxyl content determination were performed in order to determine the C(9) formulae for the studied lignins. The total antioxidant capacity of the studied lignins has been determined and compared to commercial antioxidants commonly used in thermoplastic industry.

Nanocellulose-based composites and bioactive agents for food packaging

Global environmental concern, regarding the use of petroleum-based packaging materials, is encouraging researchers and industries in the search for packaging materials from natural biopolymers. Bioactive packaging is gaining more and more interest not only due to its environment friendly nature but also due to its potential to improve food quality and safety during packaging. Some of the shortcomings of biopolymers, such as weak mechanical and barrier properties can be significantly enhanced by the use of nanomaterials such as nanocellulose (NC). The use of NC can extend the food shelf life and can also improve the food quality as they can serve as carriers of some active substances, such as antioxidants and antimicrobials. The NC fiber-based composites have great potential in the preparation of cheap, lightweight, and very strong nanocomposites for food packaging. This review highlights the potential use and application of NC fiber-based nanocomposites and also the incorporation of bioactive agents in food packaging.

Differential scanning calorimetry of phenol-formaldehyde resins cure-accelerated by carbonates

Abstract One of the drawbacks of phenol–formaldehyde (PF) resol resin is its slow cure which requires longer hot-pressing time for the manufacture of wood composite products, especially for thick fibreboard products. In this study, PF resol resin was modified with three carbonates (i.e. propylene carbonate, sodium carbonate and potassium carbonate) to accelerate the cure of the resin for the manufacture of medium density fibreboard. The thermal behaviour of carbonate-modified PF resol resins was characterized with differential scanning calorimetry (d.s.c.) using three different thermal scanning methods (single-heating rate, multi-heating rate and isothermal method). The results of the single-heating rate method were not consistent when compared to the other two methods. The rate constants were calculated with the activation energy and pre-exponential factor obtained by the multi-heating method. The calculated rate constant increased with increasing carbonate level and the temperature selected. The isothermal method revealed that the curing of propylene carbonate-modified resins follows autocatalytic kinetics while the other two additives showed n th-order kinetics with a partial autocatalytic effect.

Fibrous long-chain organic acid cellulose esters and their characterization by diffuse reflectance FTIR spectroscopy, solid-state CP/MAS 13C-NMR, and X-ray diffraction

Unsaturated and saturated organic acids with 11 and 18 carbon atoms, respectively, were used in a heterogeneous esterification reaction in the pyridine/toluene sulfonyl chloride system to prepare fibrous cellulose esters with different degrees of substitution. Highly bleached sulfite cellulose fibers were esterified during a 1- or 2-h reaction time with the following organic acids: undecylenic acid, undecanoic acid, oleic acid, and stearic acid. In all cases, the heterogeneous esterification yielded partially substituted cellulose esters retaining their fibrous structure. The substitution reaction was confirmed by diffuse reflectance infrared spectroscopy and the chemical structures of cellulose esters were identified by solid-state CP/MAS 13C-NMR (75.3 MHz). X-ray diffraction analyses showed broadening of the diffraction peaks with a higher degree of substitution of cellulose esters, which suggests structural changes within the cellulose fibers. Because the broadening peaks of X-ray spectra or the unassigned C-4 region of substituted cellulose chains in NMR spectra do not allow the calculation of dimensional changes of cellulose crystallites in cellulose esters, the lateral dimensions of crystallites in only cellulose fibers were calculated. The value derived from NMR (4.6 nm) differs by about 11% when compared with the value calculated from X-ray diffraction data (4.1 nm).

Reinforcement of Recycled Polyolefins with Wood Fibers

In this work recycled polyolefins from municipal solid wastes, composed of 95% polyethylene (PE) and 5% polypropylene (PP), are reinforced with chemico thermomechanical pulp fiber, and the resulting material is formed by compression and in jection molding. Tensile properties are presented as function of fiber concentration, fiber surface treatment with acetic anhydride and phenol-formaldehyde, and sample storage time in water. Strength and toughness of the recycled polyolefins were increased with addi tion of non-treated fiber. Addition of 30% fiber, by weight, in the polymer matrix, in creased its Young modulus up to 150%. Composites with 10 % of treated fiber showed gen erally higher tensile properties than those containing 10 % of non-treated fiber. For composites made with treated fiber, water sorption during storage time was lower and mechanical properties remained higher, compared with composites made from non- treated fiber.

Encapsulation of probiotic bacteria in biopolymeric system.

Encapsulation of probiotic bacteria is generally used to enhance the viability during processing, and also for the target delivery in gastrointestinal tract. Probiotics are used with the fermented dairy products, pharmaceutical products, and health supplements. They play a great role in maintaining human health. The survival of these bacteria in the human gastrointestinal system is questionable. In order to protect the viability of the probiotic bacteria, several types of biopolymers such as alginate, chitosan, gelatin, whey protein isolate, cellulose derivatives are used for encapsulation and several methods of encapsulation such as spray drying, extrusion, emulsion have been reported. This review focuses on the method of encapsulation and the use of different biopolymeric system for encapsulation of probiotics.

Curing kinetics of phenol formaldehyde resin and wood-resin interactions in the presence of wood substrates

The curing kinetics of resol PF resin and resin–wood interactions in the presence of wood substrates have been studied by differential scanning calorimetry (DSC) and Fourier transform infrared (FTIR) spectroscopy. The activation energy of cure of PF resin generally increases when PF resin is mixed with wood, mainly due to the decrease of the pH values resulting from the presence of wood. However, wood decreases the curing enthalpy of PF resin through diffusion and the change in the phase of the curing system, which suggests that the curing reactions reached a lower final degree of conversion for the mixtures of PF resin with wood than for the PF resin alone. Moreover, DSC curves and the variation of activation energy with conversion indicate that wood accelerates the addition reactions and retards condensation ones during the curing process of PF resin with wood. The study also revealed that almost no chemical reactions occur between PF resin and wood, but the secondary force interactions of hydroxyl groups between PF resin and wood have been detected. These most significant secondary forces can catalyze the self-condensation reactions of PF resin, although their effect is not vital on the curing kinetics of PF resin.