Front roughening in three-dimensional imbibition

We investigate the structure and dynamics of the interface between two immiscible liquids in a three-dimensional disordered porous medium. We apply a phase-field model that includes explicitly disorder and discuss both spontaneous and forced imbibition. The structure of the interface is dominated by a length scale ξ_× which arises from liquid conservation. We further show that disorder in the capillary and permeability act on different length scales and give rise to different scalings and structures of the interface properties. We conclude with a range of applications.     

Specific influence of univalent cations on the ionization of alumina-coated TiO2 particles and on the adsorption of poly(acrylic)acid

A surface counterion titration method was used to monitor the interaction of monovalents cations (Li(+), Na(+), TMA(+)) with the surface of alumina-coated TiO(2) particles in concentrated media at different pH and electrolyte concentrations. This method allows measuring separately the negative and positive contribution to the surface charge. It showed that Cl(-) and TMA(+) are indifferent ions, but Li(+) and Na(+) specifically adsorb on the non-ionized alumina surface sites. The binding sequence of cations is Li(+)>Na(+)>TMA(+) at all ionic strengths investigated and is consistent with the structure-making and structure-breaking model developed a few decades ago. Polyacrylic acid (PAA) previously neutralized with the corresponding hydroxide (LiOH, NaOH, TMAOH) has been adsorbed on the alumina surface at different pH. The polymer counterion has a significant influence on the polymer adsorption. The sequence of the surface coverage as a function of the polymer counterion follows the order Li-PAA > Na-PAA > TMA-PAA. The much higher surface coverage with Li-PAA and Na-PAA compared to TMA-PAA is explained by the specific adsorption of Li-PAA and Na-PAA on the nonionized alumina surface sites, the same way LiCl and NaCl do.     

A study on the ink-fiber interfacial interaction in waste printed paper I. The effect of a custom-designed polymeric additive on flotation de-inking of solvent-treated wastepapers

The effect of interaction between solvent and three different kinds of printed wastepaper has been studied. The solubility parameter of the solvent was found to be among the most important in order to obtain an optimum ink-fiber interfacial swelling, necessary for de-inking wastepaper. The degree of ink-fiber interfacial swelling was qualitatively estimated by examining the dispersity of ink particles using an optical microscope. FT-IR analyses were carried out to correlate the degree of dispersion and the ink composition in the printed wastepapers studied. The effect of a selective swelling solvent on the de-inking characteristics of a mixture of old wastepapers was investigated. The solvent treatment of these wastepapers prior to flotation de-inking failed to add any positive effect on the brightness of the de-inked pulp. On the other hand, the incorporation of a custom-designed polymer additive improved the pulp brightness without any solvent treatment. The same additive played a negative role in the presence of a swelling solvent. The function of the polymer additive in the flotation de-inking process is also described.     

Spectroscopic characterization of oxidized nanocellulose grafted with fluorescent amino acids

A hardwood bleached kraft pulp was oxidized by sodium hypochlorite using 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO) and sodium bromide in water as catalysts to produce oxidized fibers. These oxidized fibers were mechanically disintegrated into oxidized nano-elements which were separated from the coarse components by centrifugation to obtain oxidized nanocellulose (ONC). The ONC was then coupled with fluorescent amino acids using a two step coupling procedure. First, the ONC was activated by N-ethyl-N′-(3-dimethylaminopropyl) carbodiimide hydrochloride, forming a stable active ester in the presence of N-hydroxysuccinimide. Second, the active ester was reacted with the amino groups on the amino acids, forming an amide bond between the ONC and amino acids. The products (ONC-amino acids) were characterized by transmission electron microscopy and by different spectroscopic techniques such as absorption, emission, FTIR and XPS.     

Cellulose nanofibres by sonocatalysed-TEMPO-oxidation

The purpose of this work was to study the influence of acoustic cavitation on the oxidation of a mill bleached machine dried hardwood Kraft pulp. The oxidation of the pulp was carried out using 4-acetamido-TEMPO coupled with NaOCl/NaBr as co-oxidizer. The carboxylate content was increased by about 30% without any adverse impact on the degree of polymerization in the case of oxidations under acoustic cavitation compared to the reference without acoustic cavitation. A close correlation between the yield of nanocellulose and the carboxylate content of the oxidized pulps was observed. The individualized cellulose nanofibres were 3–4 nm in width and a few microns in length.     

Drying Characteristics-Property Correlationships in Gas-Fired Infrared Drying of Paper Obtained by Diffuse Reflectance FT-IR Spectroscopy

Introduction

Infrared (IR) drying of paper in a pilot scale has been investigated by several researchers in the past [1–3]. Both high-intensity electric heating and medium-intensity gas heating are now being used industrially either to preheat wet paper before conventional steam drying [1] or as a moisture-profile corrector just before paper sizing press [2]. Our own investigation [3] on the use of radiant energy from a gas-fired IR radiator have revealed that the drying efficiency of IR radiation is influenced by the nature of association of water molecules with cellulose in wet paper. Depending on the total moisture content of a paper, the free and bound moisture contents of paper will vary in wet paper sheet. Our previous study [3] has also confirmed that it is possible to remove free moisture more efficiently using gas-fired IR emitter operated at 1373 K rather than as 1223 K. It is reported that besides emitter temperature, the efficiency of drying also depends on the location of the emitter. In general, the efficiency is high if the emitter is installed near the preheating zone and the efficiency changes in the following order: falling rate < constant rate < preheating. Pikulik [4] compared the efficiency of hot gas impinging drying with conventional steam drying emphasizing the paper properties. The properties of a high-intensity hot gas-dried paper has been reported to be better than those of conventionally steam dried paper. An immediate quality improvement in terms of reduced moisture steaks and superior resistance to paper embrittleness was also observed when installing a high-intensity infrared drying system [5,6].     

Monitoring and characterization of ink vehicle autoxidation by inverse gas chromatography

It is now well-established that increased usage of vegetable oils in offset ink formulas aggravates the deinking problems in recycling plants during summer months. The seasonal loss of brightness of recycled paper has been ascribed to increased bonding of oxidatively aged prints to the paper surface. The progress of the oxidative aging of soya bean and linseed oils was followed by inverse gas chromatography. We first report here the rate and extent of vegetable oil oxidation, by measuring the changes in Kovats retention index as a function of the oxidation time. We then characterized the physicochemical changes accompanying the oxidation of vegetable oils from measurements of the partial heat of mixing in the infinite dilution regime.     

Donnan equilibrium and the effective charge of sodium polyacrylate

Osmometry using an external stressor is a very useful method to measure the equilibrium osmotic pressure for dilute solutions of polyelectrolyte. By taking into account the contribution of the ideal gas law, the excluded volume, the solvency effect, and the Donnan equilibrium effect on the measured pressure it is possible to estimate the effective charge of sodium polyacrylate 35 kgmol⁻¹ as a function of the polymer concentration, the pH, the ionic strength, and the presence of Ca²⁺ ion. The numerical resolution of state equations has shown that the effective charge increases with the ionic strength or with the decreasing polymer concentration, in agreement with recent theoretical models. On the other hand, the effective charge is pH-independent. This statement remains valid as long as the degree of neutralization of the polyacrylate is over 0.5. Above this degree of neutralization, any further neutralization promoted by NaOH addition leads to the condensation of the Na⁺ counterion, in agreement with the general concept of ionic condensation. The effective charge represents only 10–20% of the total number of monomer units for pH within 6 and 9 and ionic strength below 0.1 M. The polymer can tolerate the presence of Ca²⁺ at least up to a molar ratio Ca²⁺/–COOH = 0.222 without any influence on the effective charge. Received: 11 July 2000/Accepted: 23 October 2000     

Effect of fiber treatment on mechanical properties of polypropylene-wood fiber composites

Polypropylene (PP) was reinforced with chemi-thermomechanical (CTMP) pulp and wood flour. Different chemical treatment of the fiber a) polyethylene-poly-(phenyl isocyanate), b) silane A-172 and c) epolene was carried out to improve the bonding between the polymer and fiber. PP reinforced with CTMP pulp and wood flour showed a decrease in stress values as the concentration of fiber increased in the composite. Tensile modulus generally increased with filler loading and was not much affected by fiber treatment. Experimental results of the composites were compared with theoretically predicted values.     

The Use of Weissler Method for Scale-Up a Kraft Pulp Oxidation by TEMPO-Mediated System from a Batch Mode to a Continuous Flow-Through Sonoreactor

The efficiency of cellulose oxidation mediated by the 4-acetamido-TEMPO radical under ultrasonic cavitation was investigated using two ultrasonic systems: a batch lab scale ultrasonic bath with a glass reactor and a semi-continuous flow-through sonoreactor. The main objective was to explore the possibility of scaling up the production of oxidized cellulose under ultrasound, from a lab scale process to a pilot plant process, which served as a precursor for producing nanofibrils cellulose. It was found that under acoustic cavitation, the efficiency of TEMPO-mediation oxidation of native cellulose was significantly improved, particularly in the flow-through sonoreactor. In comparison with the glass reactor, the flow-through sonoreactor reduce the applied energy by 88% while increasing 7.8 times the production rate of radicals. These results enable a possibility of producing oxidized fibers for industrial applications.