Effect of marangoni stresses on the deformation and coalescence in compatibilized immiscible polymer blends

The effect of physical compatibilization on the deformation and coalescence of droplets in immiscible polymer blends is discussed. Evidence is provided for the existence of concentration gradients in block copolymers along the interface during deformation. This causes complex changes in droplet shapes during deformation and relaxation. These concentration gradients also result in Marangoni stresses, which stabilize the droplets against deformation and breakup. Coalescence experiments have been performed, varying both the compatibilizer concentration and the shear rate. Existing coalescence models have been evaluated. An empirical extension of Chesters' partially mobile interface model is presented, that treats the effects of Marangoni stresses on the coalescence process as a higher effective viscosity ratio.     

Kinetics of the peracetic acid decomposition: Part II: pH effect and alkaline hydrolysis

The effect of pH on the decomposition of peracetic acid in an aqueous solution was studied. It was found that three potential reactions, namely i) the spontaneous decomposition, ii) the hydrolysis and iii) the transition metal catalysed decomposition, are responsible for the consumption of peracetic acid. The spontaneous decomposition reaches its maximum at pH 8.2, while both the hydrolysis and metal ion catalysed decomposition increase as the pH increases. At pH 10.5 and higher, the hydrolysis becomes dominant when the metal ion catalysed decomposition is minimized by the addition of DTMPA. The kinetics of the peracetic acid hydrolysis was developed, which can very well predict the development of peracetic acid and hydrogen peroxide during the decomposition reaction.     

On the effect of treating poly(acrylic acid) with argon and tetrafluoromethane plasmas: Kinetics and degradation mechanism

Poly(acrylic acid) (PAAc) films were treated with either an argon or a tetrafluoromethane (CF₄) plasma and subsequently analyzed with X-ray photoelectron spectroscopy (XPS). PAAc films were decarboxylated during both types of plasma treatments. In addition, during the CF₄ plasma treatment, the PAAc films became fluorinated. The plasma phase during the argon plasma treatment of PAAc films was investigated with optical emission spectroscopy. It was shown that during this plasma treatment carbon dioxide, water, and possibly hydrogen were liberated from the PAAc surface. By covering the surface of PAAc films with different materials (lithium fluoride, UV fused silica, and glass) during the plasma treatment, it was possible to differentiate between photochemically induced and particle-induced changes of the surface. This method was used to show that decarboxylation during the argon plasma treatment was caused by vacuum UV radiation (wavelength < 150 nm) and the decarboxylation/fluorination during the CF₄ plasma treatment was induced by reactive fluorine-containing species from the plasma phase. Furthermore, during both processes, etching of the PAAc surface occurred. Based on these mechanisms, kinetic models were derived that could be used to describe the measured kinetic data adequately. © 1994 John Wiley & Sons, Inc.     

Polymerization of liquid propylene with a fourth‐generation Ziegler–Natta catalyst: Influence of temperature,hydrogen, monomer concentration,and prepolymerization method on powder morphology

Liquid propylene was polymerized in a 5‐L autoclave batch reactor using a commercially available TiCl₄/MgCl₂/Al(ethyl)₃/DCPDMS Ziegler–Natta catalyst, with a phthalate ester as internal electron donor. The powders from these polymerizations were characterized using laser diffraction particle size distribution (PSD) analysis, scanning electron microscopy (SEM), and bulk density measurements. These characteristics were analyzed as a function of the process conditions, including hydrogen and monomer concentration, polymerization temperature, and the prepolymerization method. It was shown that polymerization temperature influences the powder morphology to a large extent. At low temperatures, high‐density particles were obtained, showing regular shaped particle surfaces and low porosities. With increasing temperature, the morphology gradually was transferred into a more open structure, with irregular surfaces and poor replication of the shape of the catalyst particle. When using a prepolymerization step at a relatively low temperature, the morphology obtained was determined by this prepolymerization step and was independent from conditions in main polymerization. The morphology obtained was the same as that observed after a full polymerization at temperature. Even when using a short polymerization at an increasing temperature, the morphology was strongly influenced by the initial conditions. The effect of variation in hydrogen concentration supported the conclusion that the initial polymerization rate determines the powder morphology. In the absence of hydrogen, high bulk densities, and regularly shaped particles were obtained, even at high temperatures. With increasing hydrogen concentration, the reaction rates increased rapidly, and with that changed the morphology. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1421–1435, 2003     

Relationship of peroxide value and thiobarbituric acid value to development of undesirable flavor characteristics in fats

The peroxide value and thiobarbituric acid value were compared with the flavor score for a series of different types of fats, with and without added monoglyceride and with and without different stabilizers. The data indicated that the flavor score cannot be estimated for any given fat from either the peroxide value or the thiobarbituric acid value. Either can be used to follow the development of off flavors in a given product or formulation but the relative level may vary from product to product. Presented at the AOCS Meeting in Minneapolis, 1963.     

High-Temperature Stiffness and Damping Measurements to Monitor the Glassy Intergranular Phase in Liquid-Phase-Sintered Silicon Carbides

Detailed stiffness and internal friction ( Q ⁻¹) versus temperature curves were obtained for liquid-phase-sintered silicon carbides using advanced resonant beam analysis up to 1400°C. As-sintered materials display a stable Q ⁻¹-peak near 1100°C, superimposed on an increasing background. The change of stiffness associated with the damping peak is quantitatively related to the amount of matter in pockets of the amorphous intergranular phase in which the refractory SiC matrix grains are embedded. The successful removal of the amorphous pockets by annealing at 1900°C is deduced from the disappearance of the damping peak and confirmed with transmission electron microscopy.     

Experimental research and prediction of the effect of chemical and biogenic sulfuric acid on different types of commercially produced concrete sewer pipes

New equipment and procedures for chemical and microbiological tests, simulating biogenic sulfuric acid corrosion in sewerage systems, are presented. Subsequent steps of immersion and drying, combined with mechanical abrasion, were applied to simulate events occurring in sewer systems. Both chemical and microbiological tests showed that the aggregate type had the largest effect on degradation. Concrete with limestone aggregates showed a smaller degradation depth than did the concrete with inert aggregates. The limestone aggregates locally created a buffering environment, protecting the cement paste. This was confirmed by microscopic analysis of the eroded surfaces. The production method of concrete pipes influenced durability through its effect on W/C ratio and water absorption values. In the microbiological tests, HSR Portland cement concrete performed slightly better than did the slag cement concrete. A possible explanation can be a more rapid colonisation by microorganisms of the surface of slag cement samples. A new method for degradation prediction was suggested based on the parameters alkalinity and water absorption (as a measure for concrete porosity).     

Segregation in beds of large particles at high velocities

In some industrial fluidized bed processes, notably coal combustion, the bed contains a very wide size range (50 – 5000 μm) of equal density particles. In others the particles change their density as the reaction proceeds, giving a bed of particles having similar sizes but densities varying by a factor of up to 2.

Experiments have been done in a bed 0.29 m diam. at velocities up to 5 m/s, using coarse particles up to 6 mm. They show that segregation by density difference can be reduced to negligible proportions by using high velocities, but that segregation by size appears to be an intrinsic feature of coarse particle systems at all velocities when a very wide size range is present. A tentative form of equation is proposed for segregation by size; the equations of Rowe are useful predictors for segregation by density difference.     

Liquid spouting of pulp fibers in a conical vessel

Pulp fibers can be spouted in water in a conical vessel. The entities which are spouted are fiber flocs rather than individual fibers. Synthetic fibers, which do not flocculate, cannot be spouted. For comparison, rigid spherical particles were spouted with water in the same conical vessel. Liquid spouting of rigid particles was similar to gaseous spouting. For pulp spouting, the minimum spouting velocity is proportional to the mass of fibers in the bed and inversely proportional to the diameter of the inlet. For rigid particles, the minimum spouting velocity is proportional to the height of the bed and inversely proportional to the square of the diameter of the inlet. A model for the minimum spouting velocity was developed for pulp spouting.     

Large-scale SRAM-based IP lookup architectures using compact trie search structures

SRAM-based pipelined architectures for high-speed IP lookup using Field Programmable Gate Arrays (FPGAs) has recently attracted a great deal of attention from researchers. Due to the limited amount of on-chip memory and the number of I/O pins of FPGAs, compact data structures providing high memory efficiency are in great demand.