Limited information exists regarding the processing parameters and extent of reinforcing potential natural fibers have in polymer matrices. The five natural fiber mats studied were low shive flax, mid shive flax, high shive flax, hemp and kenaf. The parameters characterized were fiber size, wax content, surface contact angle, and shive content. The compressive force and unsaturated permeability was measured for each mat, and composites were constructed and tested using selected mats in a soy-based polyurethane (PU) matrix. All mats exhibited a viscoelastic behavior under compression, and an increase in shive content correlated with an increase in relaxation. The presence of shive and larger fiber size increased the permeability. Higher wax content and contact angle lowered the permeability. The mechanical properties for all composites performed better than the neat PU, showing there was matrix to fiber adhesion and load transfer. Hemp outperformed the other fibers studied in all mechanical tests.

No description available.

No description available.

No description available.

A wood surface, which is exposed to a high temperature condition, can experience inactivation. Surface inactivation results in reduced ability of an adhesive to properly wet, flow, penetrate, and cure. Thus, an inactivated wood surface does not bond well with adhesives. The changes in surface chemistry, wettability, and adhesion of inactivated wood surfaces, including heartwood of yellow-poplar (Liriodendron tulipifera) and southern pine (Pinus taeda), were studied. Wood samples were dried from the green moisture content condition in a convection oven at five different temperature levels ranging from 50 to 200 °C. The comparative characterization of the surface was done by X-ray photoelectron spectroscopy (XPS), sessile drop wettability, and fracture testing of adhesive bonds. The oxygen to carbon ratio (O/C) decreased and the C1/C2 ratio increased with drying temperature. The C1 component is related to carbon-carbon or carbon-hydrogen bonds, and the C2 component represents single carbon-oxygen bond. A low O/C ratio and a high C1/C2 ratio reflected a high concentration of non-polar wood components (extractives/VOCs) on the wood surface, which modified the wood surface from hydrophilic to more hydrophobic. Wettability was directly related to the O/C ratio and inversely related to the C1/C2 ratio. Contact angle decreased with time and increased with the temperature of exposure. Southern pine had a lower wettability than yellow-poplar, which was due to a greater concentration of non-polar hydrocarbon-type extractives and heat-generated volatiles on the surface. Solvent extraction prior to drying did not improved wettability, whereas, extraction after drying improved wettability. A contribution of extractives migration and VOCs generation played a significant role in the heat-induced inactivation process of southern pine. The maximum strain energy release rate (Gmax) showed that surface inactivation was insignificant for yellow-poplar when exposed to drying temperatures < 187°C. The southern pine was most susceptible to inactivation at drying temperatures > 156°C, particularly when bonded with phenol-formaldehyde (PF) adhesive. Chemical treatments improved the wettability of inactivated wood surfaces, but an improvement in adhesion was not evident for specimens bonded with polyvinyl-acetate (PVA) adhesive. NaOH surface treatment was most effective for improving adhesion of the PF adhesive bond. / Ph. D.

No / OBJECTIVES: Cocrystallization of sulfadimidine (SDM) with suitable coformers, such as 4-aminosalicylic acid (4-ASA), combined with changes in the crystal habit can favourably alter its physicochemical properties. The aim of this work was to engineer SDM : 4-ASA cocrystals with different habits to investigate the effect on dissolution, and the derived powder properties of flow and compaction. METHODS: Cocrystals were prepared in a 1 : 1 molar ratio by solvent evaporation using ethanol (habit I) or acetone (habit II), solvent evaporation followed by grinding (habit III) and spray drying (habit IV). KEY FINDINGS: Powder X-ray diffraction showed Bragg peak position was the same in all the solid products. The peak intensity varied, indicating different preferred crystal orientation confirmed by SEM micrographs: large prismatic crystals (habit I), large plate-like crystals (habit II), small cube-like crystals (habit III) and microspheres (habit IV). The habit III exhibited the fasted dissolution rate; however, it underwent a polymorphic transition during dissolution. Habits I and IV exhibited the highest Carr's compressibility index, indicating poor flowability. However, habits II and III demonstrated improved flow. Spray drying resulted in cocrystals with improved compaction properties. CONCLUSIONS: Even for cocrystals with poor pharmaceutical characteristics, a habit can be engineered to alter the dissolution, flowability and compaction behaviour.

Yes / Objectives: Cocrystallization of sulfadimidine (SDM) with suitable coformers, such as 4-aminosalicylic acid (4-ASA), combined with changes in the crystal habit can favourably alter its physicochemical properties. The aim of this work was to engineer SDM:4-ASA cocrystals with different habits in order to investigate the effect on dissolution, and the derived powder properties of flow and compaction. Methods: Cocrystals were prepared in a 1:1 molar ratio by solvent evaporation using ethanol (habit I) or acetone (habit II), solvent evaporation followed by grinding (habit III) and spray-drying (habit IV). Key findings: Powder X-ray diffraction showed Bragg peak position was the same in all the solid products. The peak intensity varied, indicating different preferred crystal orientation confirmed by SEM micrographs: large prismatic crystals (habit I), large plate-like crystals (habit II), small cube-like crystals (habit III) and microspheres (habit IV). The habit III exhibited the fasted dissolution rate; however, it underwent a polymorphic transition during dissolution. Habits I and IV exhibited the highest Carr’s compressibility index, indicating poor flowability. However, habits II and III demonstrated improved flow. Spray drying resulted in cocrystals with improved compaction properties. Conclusions: Even for cocrystals with poor pharmaceutical characteristics, a habit can be engineered to alter the dissolution, flowability and compaction behavior. / Science Foundation Ireland. Grant Number: SFI/12/RC/2275

The goal of this work is to change the wettability of a carbonate rock from oil wet-mixed-wet towards water-wet at high temperature and high salinity. Only simple surfactant systems (single surfactant, dual surfactants) in dilute concentration were tried for this purpose. It was thought that the change in wettability would help to recover more oil during secondary surfactant flood as compared to regular waterflood. Three types of surfactants, anionic, non-ionic and cationic surfactants in dilute concentrations (<0.2 wt%) were used. Initial surfactant screening was done on the basis of aqueous stability at these harsh conditions. Contact angle experiments on aged calcite plates were done to narrow down the list of surfactants and spontaneous imbibition experiments were conducted on field cores for promising surfactants. Secondary waterflooding was conducted in cores with and without the wettability altering surfactants. It was observed that barring a few surfactants, most were aqueous unstable by themselves at these harsh conditions. Dual surfactant systems, a mixture of a non-ionic and a cationic surfactant increased the aqueous stability of the non-ionic surfactants. One of the dual surfactant system, a mixture of Tergitol NP-10 and Dodecyl trimethyl ammonium bromide, proved very effective for wettability alteration and could recover 70-80% of OOIP during spontaneous imbibition. Secondary waterflooding with the wettability altering surfactant (without alkali or polymer) increased the oil recovery over the waterflooding without the surfactants (from 29% to 40% OOIP). Surfactant adsorption calculated during the coreflood showed an adsorption of 0.24 mg NP-10/gm of rock and 0.20 mg DTAB/gm of rock. A waterflood done after the surfactant flood revealed change in the relative permeability before and after the surfactant flood suggesting change in wettability towards water-wet. / text

Indiana University-Purdue University Indianapolis (IUPUI) / Background: Numerous studies have reported the effect of long-term use of calcium hydroxide Ca(OH)2 to dentin. Nevertheless, there is little information available about the effect of Ca(OH)2 on wettability to the dentin. Objective: To investigate the effect of Ca(OH)2 application on dentin for two and four weeks on the wettability of two root canal sealers. Methods: Polished caries-free human dentin discs (n = 156) were allocated into 12 groups; G1 and G3 had two weeks’ treatment, G4 and G6, four weeks treatment. G1 and 101 G4 were treated with sterile water. G2, G3, G5 and G6 were treated with Ca(OH)2. G1, G3, G4, and G6 were irrigated with 6.0-percent NaOCl and 17-percent EDTA while G2, and G5 were irrigated with sterile water. Then, contact angles between Tubli-Seal and the treated dentin surfaces were measured. G7 and G12 were treated in the same fashion but were treated with BC sealer. Surface morphology evaluation of G1 and G6 was carried out by scanning electron microscopy (SEM) and energy-dispersive x-ray spectroscopy (EDX). Statistics were performed using three-way ANOVA and pair-wise comparisons between groups (α = 0.05). Results: Tubli-Seal (G1 through G6) had significantly smaller values for contact angles than BC sealer (G7 through G12) (p < 0.05). For the Tubli-Seal groups (G1 through G6), G4 had the highest mean of contact angles at 104.9 ± 1.9°, whereas G5 presented the lowest mean of contact angles at 85.4 ± 15.1. For the BC sealer groups (G7 through G12), G10 had the highest mean of contact angles at 145.4 ± 1.3°, while G11 demonstrated the lowest mean of contact angles at 130.2 ± 2.6°. Groups with Ca(OH)2 treatment with water irrigation (G2, 5, 11) had significantly lower contact angle than groups with Ca(OH)2 with chemical irrigation (G3, 6, 12) (p < 0.05), except G8, 9. According to SEM and EDX, water irrigation solution showed higher remaining Ca(OH)2 than irrigation with the chemical solution while Ca(OH)2 with chemical irrigation 102 demonstrated no Ca(OH)2 remaining after irrigation, similar to the surface of the control group. Conclusion: Within the limitations of this study, Tubli-seal has better wettability on dentin than BC sealer. Remaining calcium hydroxide demonstrated a trend toward decreased contact angle between dentin and root canal sealers. Moreover, two-minute irrigation with 6-percent NaOCl and 17-percent EDTA can remove calcium hydroxide from polished dentin surfaces.

This Thesis explores physical phenomena characteristic for thin liquid films and small droplets of simple and complex liquids on solid substrates for which wettability and capillarity control their statical and dynamical properties. We start by discussing the general concepts of wettability and capillarity and introduce the common mathematical framework of the lubrication approximation for studies of thin liquid films and small contact angle drops. We demonstrate the derivation of the generic equation describing the evolution of a film of simple liquid from the Navier-Stokes equations. We show how this model can be further extended to incorporate various effects relevant to the case of complex liquids. The results described in the Thesis comprise three projects with the common main theme of the influence of wettability and capillarity on the statics and dynamics of the studied systems, namely (i) Evaporating sessile droplets fed through the solid substrate - a geometry that allows us to discuss steady states of the system and their role in the time evolution of freely evaporating droplets without influx in an isothermal case; (ii) The influence of a solute--dependent wettability on the stability, static and dynamical properties of thin films and drops of non-volatile mixtures, suspensions and solutions; (iii) A parameter-passing scheme between particle-based Molecular Dynamics simulations and the continuum lubrication model which allows us to discuss equilibrium properties of small polymeric droplets. We present the physical questions arising in the three systems and discuss approaches and results as well as possible extensions.