Alvaro Tejado

Films Prepared from Electrosterically Stabilized Nanocrystalline Cellulose

Electrosterically stabilized nanocrystalline cellulose (ENCC) was modified in three ways: (1) the hydroxyl groups on C2 and C3 of glucose repeat units of ENCC were converted to aldehyde groups by periodate oxidation to various extents; (2) the carboxyl groups in the sodium form on ENCC were converted to the acid form by treating them with an acid-type ion-exchange resin; and (3) ENCC was cross-linked in two different ways by employing adipic dihydrazide as a cross-linker and water-soluble 1-ethyl-3-[3-(dimethylaminopropyl)] carbodiimide as a carboxyl-activating agent. Films were prepared from these modified ENCC suspensions by vacuum filtration. The effects of these three modifications on the properties of films were investigated by a variety of techniques, including UV-visible spectroscopy, a tensile test, thermogravimetric analysis (TGA), the water vapor transmission rate (WVTR), and contact angle (CA) studies. On the basis of the results from UV spectra, the transmittance of these films was as high as 87%, which shows them to be highly transparent. The tensile strength of these films was increased with increasing aldehyde content. From TGA and WVTR experiments, cross-linked films showed much higher thermal stability and lower water permeability. Furthermore, although the original cellulose is hydrophilic, these films also exhibited a certain hydrophobic behavior. Films treated by trichloromethylsilane become superhydrophobic. The unique characteristics of these transparent films are very promising for potential applications in flexible packaging and other high-technology products.

Energy requirements for the disintegration of cellulose fibers into cellulose nanofibers

Cellulose nanofibers have a bright future ahead as components of nano-engineered materials, as they are an abundant, renewable and sustainable resource with outstanding mechanical properties. However, before considering real-world applications, an efficient and energetically friendly production process needs to be developed that overcomes the extensive energy consumption of shear-based existing processes. This paper analyses how the charge content influences the mechanical energy that is needed to disintegrate a cellulose fiber. The introduction of charge groups (carboxylate) is achieved through periodate oxidation followed by chlorite oxidation reactions, carried out to different extents. Modified samples are then subjected to different levels of controlled mechanical energy and the yields of three different fractions, separated by size, are obtained. The process produces highly functionalized cellulose nanofibers based almost exclusively on chemical reactions, thus avoiding the use of intensive mechanical energy in the process and consequently reducing drastically the energy consumption.

Why does paper get stronger as it dries

Surprisingly the strength of wet paper is still poorly understood. Here we show that the traditional explanation of the strength of wet paper is incorrect. Observations that the capillary force in fiber crossings in wet paper approaches zero as the water is evaporated show that they are not responsible for the strength of wet paper. Instead we present evidence that fiber entanglements and friction are the cause. Like paper, films made of nanotubes, nanorods, nanofibers or nanoribbons also consist of randomly oriented fibers, and this field may well benefit from an increased knowledge of paper properties.

Simulation of tagasaste pulping using soda-anthraquinone.

In this work, published experimental result data of the pulping of tagasaste (Chamaecytisus proliferus L.F.) with soda and anthraquinone (AQ) have been used to develop a model using a neural network. The paper presents the development of a model with a neural network to predict the effects that the operational variables of the pulping reactor (temperature, soda concentration, AQ concentration, time and liquid/solid ratio) have on the properties of the paper sheets of the obtained pulp (brightness, traction index, burst index and tear index). Using a factorial experimental design, the results obtained with the neural network model are compared with those obtained from a polynomial model. The neural network model shows a higher prediction precision that the polynomial model.

Salt-induced acceleration of chemical reactions in cellulose nanopores

Chemical reactions in charged nanopores, such as present in cellulose fibers, can be accelerated by adding an inert salt, that does not participate in the reaction. Due to a Donnan-like equilibrium between ions inside and outside the pores, the concentration of co-ions in the nanopores (having a charge of the same sign as that of the pore wall), is lower than the concentration in the bulk. The co-ion concentration in pores can be increased by adding an inert salt, which shifts the Donnan equilibrium. The increased concentration of reactants in pores results in faster reaction kinetics. Reactions of cellulose with periodate confirm these predictions.