INFLUENCES OF INTERFACIAL CONVECTION AND PHYSICAL PROPERTIES OF DESICCANT SOLUTIONS ON THE MASS TRANSFER PERFORMANCE OF ABSORPTION SYSTEMS

In order to investigate the mass transfer phenomenon of the absorption of water vapor in desiccant solutions, a system of absorption cell was designed. The gradient in surface tension can result from the contact process between the desiccant solution and water vapor. This induced interfacial disturbance will affect the mass transfer performance. The experimental results demonstrate that the theoretical mass transfer coefficients predicted by boundary layer theory are less than those of the experimental values. In addition, the mass transfer performance of the absorption system can be enhanced by adding ethanol to the absorbent solutions. In order to describe the level of mass transfer performance affected by the interfacial convection resulting from the addition of ethanol, the enhancement factor was defined in this study. The enhancement factor is from 1.26 to 1.56 for adding ethanol to DEG (diethylene glycol) solution, and from 1.36 to 1.61 for adding ethanol to TEG (triethylene glycol) solution.     

A Review of: “THERMAL CHARACTERISTICS OF TUMORS”, edited by R.K. Jain and P.M. Gullino (Volume 335 of the Annals of the New York Academy of Sciences,New York,New York 10021, 1980, 542 pp. $95.00, ISBN 0-89766-046-3).

A relationship has been derived for diffusion of an associating solute forming a dimer complex. Experimental data reported in this investigation for diffusion of acetic acid in carbon tetra chloride, benzene and toluene indicate dimer formation of acetic acid molecules while diffusing into the non-associating solvents.     

Ordered mesoporous silica prepared by quiescent interfacial growth method - effects of reaction chemistry

Acidic interfacial growth can provide a number of industrially important mesoporous silica morphologies including fibers, spheres, and other rich shapes. Studying the reaction chemistry under quiescent (no mixing) conditions is important for understanding and for the production of the desired shapes. The focus of this work is to understand the effect of a number of previously untested conditions: acid type (HCl, HNO₃, and H₂SO₄), acid content, silica precursor type (TBOS and TEOS), and surfactant type (CTAB, Tween 20, and Tween 80) on the shape and structure of products formed under quiescent two-phase interfacial configuration. Results show that the quiescent growth is typically slow due to the absence of mixing. The whole process of product formation and pore structuring becomes limited by the slow interfacial diffusion of silica source. TBOS-CTAB-HCl was the typical combination to produce fibers with high order in the interfacial region. The use of other acids (HNO₃ and H₂SO₄), a less hydrophobic silica source (TEOS), and/or a neutral surfactant (Tweens) facilitate diffusion and homogenous supply of silica source into the bulk phase and give spheres and gyroids with low mesoporous order. The results suggest two distinct regions for silica growth (interfacial region and bulk region) in which the rate of solvent evaporation and local concentration affect the speed and dimension of growth. A combined mechanism for the interfacial bulk growth of mesoporous silica under quiescent conditions is proposed.     

Effect of substrate curvature on residual stresses and failure modes of an air plasma sprayed thermal barrier coating system

A set of aerofoil shaped air plasma sprayed thermal barrier coated (APS-TBC) specimens were adopted in this paper to investigate the stress distributions in the ceramic top coat (TC) and the thermally grown oxide (TGO), the mechanism of local crack generation and propagation at the TC/BC (bond coat) interface. The failure mode of the TBC system, the distribution of asperities at TC/BC interface, thickness of the TC and BC, and the TC microstructure were found to be influenced by substrate curvature. Residual stress was therefore measured across the thickness of the TC, along the undulating TGO and mapped at locations of asperities where failure tended to occur to interpret the initiation of local failure. The role of the TGO was investigated via its chemical bonding with the TC and the decohesion occurring at the TGO/BC interface. The crack propagation at the interface has been discussed with respect to the macro-failure of the TBC system.     

NOVEL LOW-COST JUTE–POLYESTER COMPOSITE. II. SEM OBSERVATION OF THE FRACTURED SURFACES

The scanning electron micrographs (SEM) were taken at different magnifications with respect of the fractured surfaces of the polymer composites prepared from unsaturated polyester resin and jute sliver with 60% fiber loading by weight. The composite specimens were prepared using both untreated (control) and chemically modified (bleached) jute fibers by solution impregnation and hot curing methods and are designated as JPH-60(C) and JPH-60(B), respectively. The method of preparation of the composite specimens have been discussed. The specimens were subjected to tensile and flexural tests and the fractured surfaces were observed under SEM as stated. The fiber surface morphology was also studied from the SEM photographs in the case of the control and bleached jute filaments. The SEM photographs of the fractured surfaces of the composites showed varied extents of fiber pull-outs under both tensile and flexural failure modes. The nature of interfacial adhesion has been discussed on the basis of the SEM study. A good correlation between the SEM study and the mechanical strength properties of the composites could be established. Exceptionally high flexural strength of the composites JPH-60(B) compared to JPH-60(C) could be explained from the SEM study.     

Effects of surface modification on properties of nanocapsules for self-healing materials

Abstract

Urea formaldehyde (UF) nanocapsules used as self-healing materials were prepared by interfacial polymerisation method using modified aliphatic amine (HB-1618) and UF resin as core and shell materials respectively. Silane coupling agent KH560 was used to modify the surface of UF nanocapsules. Fourier transform infrared spectra (FTIR) results indicated the core materials had been successfully encapsulated in UF shell; moreover, physical or chemical combinations were observed between the surface of nanocapsules and KH560. The analyses of thermal stability and mechanical properties revealed that addition of KH560 significantly improved the thermal stability, tensile strength and elastic property. Scanning electron microscope (SEM) results indicated that the addition of KH560 led to an excellent interfacial adhesion between the surface of nanocapsules and resin matrix, thus improving the ability of self-healing, beneficial for high levels of healing efficiency in the matrix materials.     

Nanostructured CeO2 microspheres synthesized by a novel surfactant-free emulsion

Nanostructured CeO₂ microspheres with an average diameter of 11 μm were prepared by a novel surfactant-free emulsion for the first time. Scanning electron microscopy (SEM), X-ray diffraction (XRD) and Brunauer-Emmet-Teller (BET) measurements were used to characterize the products. The images of SEM showed that the CeO₂ microspheres consisted of petal-like nanostructures with petal thickness in a range of 60 nm to 100 nm. The BET measurements showed the specific surface area of the CeO₂ microspheres exceeded 43 m²/g. The XRD analysis indicated the nanostructured CeO₂ microspheres were of cubic lattice. A possible mechanism of an interfacial precipitation reaction with the droplets of solid-stabilized emulsion as templates was proposed.     

Evaluation of imbedded fiber retraction phenomenological models for determining interfacial tension between molten polymers

In this work, the interfacial tension for several polymer pairs, namely polypropylene/polystyrene (PP/PS), PP/polycarbonate (PC), PP/polyamide 6 (PA-6) and low density polyethylene (LDPE) and ethylene vinyl alcohol copolymer (EVOH) was evaluated as a function of temperature using the imbedded fiber retraction method (IFR). Two phenomenological models were used and compared to infer the interfacial tension from the evolution of the imbedded fiber back into a sphere: [Carriere CJ, Cohen A, Arends CB. J Rheol 1989;33:681-9. [1] and Tjahjadi M, Ottino JM, Stone HA. AIChE J 1994;40:385-94. [2]]. It was shown that Carriere et al.'s model overestimates the value of interfacial tension whereas Tjahjadi et al.'s model leads to results that corroborate the ones obtained using other experimental methods. A method to further increase the accuracy of Tjahjadi et al.'s model was proposed. Using this method the interfacial tension for the different polymer pairs studied was evaluated and shown to decrease linearly with increasing temperature.     

Shear-induced interactions in blends of HMMPE containing a small amount of thermotropic copolyester HBA/HQ/SA

Shear-induced interactions between high molecular mass polyethylene (HMMPE) melt and a thermotropic liquid crystalline copolyester, HBA/HQ/SA (TLCP) were investigated using large amplitude oscillatory shear and capillary shear. Polarized optical microscopy (POM) observations show that the mono-domain nematic TLCP droplets embedded inside a HMMPE melt may be readily elongated using large amplitude oscillatory shear. The HMMPE melt adjacent to the elongated TLCP filament was observed to crystallize faster than that in the matrix away from the interface. TEM analysis on the 1 wt% TLCP/HMMPE blend quenched after capillary shear shows that there are strong interfacial interactions between the elongated TLCP filament and the HMMPE matrix. Long range PE lamellae orientational order up to 2 μm away from the TLCP filament surface were observed, with all the lamellae surface normal parallel to the TLCP fiber. Additionally, a strong interfacial compatibility between the TLCP filament and the HMMPE matrix with an interfacial thickness of ∼30 nm has also been observed. The enhanced interfacial compatibility is attributed to the -CH₂- group interactions due to chain alignment in both components at their interface. These results provide a fundamental insight to other TLCP containing thermoplastics where compatibilities may be present due to segmental interactions.     

Approximate migration coefficient of percolated interfacial transition zone by using the accelerated chloride migration test

In this study, the electrochemical technique is applied to accelerate chloride ion migration in cement-based material to estimate its migration coefficient. In order to investigate the chloride migration coefficient of percolated interfacial transition zone (ITZ) on the chloride migration coefficient of specimen, specimens with cylindrical aggregates of the same height as the specimen were cast and tested. In this study, the volume fraction of aggregate is constant and the varied lateral surface area of the aggregate cylinder was obtained by using different diameters and number of aggregate. The chloride migration coefficient of cement-based material was determined experimentally as a function of the lateral surface area of aggregate. A model obtained for the migration coefficient of cement-based material and the regression analysis are used to determine the approximate chloride migration coefficient of the percolated ITZ. Based on the experimental and regression analytical results, the approximate percolated ITZ migration coefficient is 40.6, 35.5, and 37.8 times of the altered migration coefficient of matrix mortar for the water/cement (w/c) ratio of 0.35, 0.45, and 0.55, respectively.