Synthesis and characterization of butyl acrylate graft sodium salt of partially carboxymethylated starch

Graft copolymers were synthesized by graft copolymerization of butyl acrylate (BA) onto sodium salt of partially carboxymethylated starch (Na‐PCMS). Ceric ammonium nitrate (CAN), a redox initiator, was used for initiation of graft copolymerization reaction. All the experiments were run with Na‐PCMS having degree of substitution, DS = 0.35. The grafting reaction was characterized by parameters such as % total conversion (%Ct), % grafting (%G), % grafting efficiency (%GE), and % add‐on. Graft copolymers were characterized by infrared spectral analysis and scanning electron microscopy. Variables affecting graft copolymerization reaction such as nitric acid concentration, reaction time, reaction temperature, and ceric ion concentration were investigated. The results revealed that 0.3M CAN as initiator, 0.3M HNO₃, with reaction time 4–4.5 h at 25–30°C were found as suitable parameters for maximum yield of graft copolymerization reaction. © 2006 Wiley Periodicals, Inc. JAppl Polym Sci 102: 3334–3340, 2006     

Frequency distributions of breaking load,tenacity, and ratio of cell wall thickness to ribbon width for single cotton fibers

Analysis of the frequency distributions of breaking load, tenacity, and ratio of cell wall thickness to ribbon width (C/R) for single cotton fibers in this study has indicated that they can all be represented by β-distributions. This suggests that a parallel model of element configurations exists in which there is a uniform distribution of elemental strengths in single cotton fibers before as well as after slack mercerization. In the case of breaking load and tenacity, the distributions are positively skewed and the skewness decreases on slack mercerization, suggesting that quite a few potentially weak places have been either completely removed or at least strengthened. The changes in C/R ratio on slack mercerization for cottons having a range of maturity have been examined and discussed. The dependence of properties such as breaking load, tenacity, and linear density on cell wall to ribbon width ratio (C/R) have also been studied.     

Adsorption of lipopolysaccharide on carbon sieves

Adsorption of lipopolysaccharide, LPS, on carbon sieves Carboxen 1003 and Carboxen 1010 has been studied. LPS adsorption kinetics is initially faster on smaller size (1-10 μm) particles of predominantly microporous Carboxen 1010 compared to Carboxen 1003 (150-200 μm) particles. However, the adsorption capacity of micro/meso/macroporous Carboxen 1003 by LPS is higher than that of Carboxen 1010 since the former carbon has wider pores that can accommodate large lipopolysaccharide molecules or their agglomerates. Carboxen 1010 probably adsorbs LPS mainly on the external (macropore) surface.     

HYDRODYNAMIC STUDIES IN FISCHER-TROPSCH DERIVED WAXES IN A BUBBLE COLUMN

Gas hold-up and Sauter mean bubble diameter measurements were made in a 0.051 m diameter by 3 m long glass bubble column in the system, nitrogen-molten wax, with three different waxes (paraffin wax FT-300, Sasol's Arge wax and Mobil's reactor wax). Paraffin wax has a tendency to foam and gas hold-up is a strong function of gas distributor type, temperature and start-up procedure, whereas the reactor waxes do not foam and are much less affected by these variables, In experiments at 265°C with a 1.85 mm single hole orifice plate distributor the gas hold-ups were nearly the same for all three waxes. However, significant differences in Sauter mean bubble diameters were obtained in experiments with different waxes; FT-300 wax produced the smallest Sauter mean bubble diameters whereas Mobil's reactor wax produced the largest bubbles. Addition of 1-octadecanol and octadecanoic acid (up to 10wt%) to the FT-300 paraffin wax caused an increase in gas hold-up and a delay in the foam break-up in runs at 265°C with the 1.85 mm orifice plate distributor.     

Novel isocyanate-free self-curable cathodically depositable epoxy coatings: Influence of epoxy groups on coating properties

Novel self-curable cathodically depositable coatings were developed from glycidyl functional epoxy ester-acrylic graft co-polymer (EEAG) without using any external crosslinking agents. The EEAG-amine adducts (EEAGAs) were prepared by reacting EEAG with varying amount of diethanolamine (DEoA) which are neutralized with acid and dispersed in deionised water to give stable dispersion for cathodic electrodeposition (CED) coatings. The dispersions were cathodically electrodeposited on phosphated steel panels and thermally cured to give uniform coating. The coatings were evaluated for different mechanical, chemical and corrosion resistance properties. The coatings were evaluated for their thermal properties using thermo gravimetric analysis (TGA). The final properties of the coatings were found to be affected by the amount of amine reacted with epoxy. The coating films showed good overall performance properties for their use in coating industry.     

Viscosity of binary mixtures. I. mono-, di-, and tri-n-butyl and -n-octylamine with cyclohexane

Viscosities for six binary mixtures of n-butylamine, di-n-butylamine, tri-n-butylamine, n-octylamine, di-n-octylamine, and tri-n-octylamine with cyclohexane have been measured at 303.15 K with an Ubbelohde suspendedlevel viscometer. Deviations of viscosities from a rectilinear dependence on mole fraction are attributed to H-bonding and to the size of alkylamine compounds. The application of the Eyring's theory of activation energy is examined. The free volume theory of Prigogine-Flory-Patterson (PFP) and the experimental excess enthalpy have been used to estimate excess viscosity ln = (ln / ₁ ⁰ – x ₂ ln ₂ ⁰ / ₁ ⁰ ) and corresponding free volume, enthalpy, and entropy contributions for five binary mixtures of tri-n-alkylamine: triethyl, tripropyl, tributyl, trihexyl, and trioctylamine with cyclohexane. A comparison of experimental and theoretical excess viscosities indicates a failure of the PFP theory when two components of the mixture differ considerably in size. The size difference contribution to excess viscosity is related to (V ₂ ^*1/2 – V ₁ ^*1/2 ), where V ₁ ^* and V ₂ ^* are hard-core volumes of two components of the mixture.     

INTRODUCTION TO INCONEL ALLOY 740: AN ALLOY DESIGNED FOR SUPERHEATER TUBING IN COAL-FIRED ULTRA SUPERCRITICAL BOILERS

1. IntroductionW hile w orldw ide environm entalrestrictionsare requiring pow ercom paniesto reduce SO x,N O x andCO 2 em issions, econom ic pressuresare sim ultaneously necessitating im provem entsin the therm aleffi-ciency ofallcoal-fired plants. A ddin…     

A century of discoveries, inventors, and new nickel alloys

The 20th century was an explosive period for the growth of the nickel industry beginning in 1906 with the development of Monel^® metal. What followed over the next 100 years was the invention of hundreds of new alloys uniquely designed for scores of applications in a multitude of industries. This paper acknowledges a number of the prolific inventors who pioneered new fields of alloy development. It also high-lights a long list of major metallurgical discoveries made by the metallurgists of the International Nickel Company.     

Studying single nanocrystals under high pressure using an x-ray nanoprobe

In this report, we demonstrate the feasibility of applying a 250-nm focused x-ray beam to study a single crystalline NbSe(3) nanobelt under high-pressure conditions in a diamond anvil cell. With such a small probe, we not only resolved the distribution and morphology of each individual nanobelt in the x-ray fluorescence maps but also obtained the diffraction patterns from individual crystalline nanobelts with thicknesses of less than 50 nm. Single crystalline diffraction measurements on NbSe(3) nanobelts were performed at pressures up to 20 GPa.     

Ontogenetic changes in pharyngeal morphology correlate with a diet shift from arthropods to dreissenid mussels in round gobies (Neogobius melanostomus)

The potential of predators to regulate populations of dreissenid mussels (Dreissena polymorpha and Dreissena rostriformis bugensis) has been addressed since early in the dreissenid invasion of North America. Round gobies (Neogobius melanostomus) larger than approximately 60 mm have been shown to prey extensively on dreissenids, whereas smaller round gobies feed mainly on aquatic insects and crustaceans. We propose that ontogenetic changes in pharyngeal morphology may contribute to this diet shift in round gobies. Pharyngeals of 69 round gobies ranging from 31 to 164 mm total length were investigated using light microscopy and scanning electron microscopy. Areas of lower pharyngeals and pharyngobranchial 2 increased allometrically with fish length. Pharyngeals of round gobies smaller than 50 mm contained narrow (< 0.1 mm diameter) papilliform teeth that are consistent with eating soft-bodied prey. By the time round gobies reached approximately 80 mm in length, pharyngeals contained larger diameter (0.3-0.5 mm) molariform teeth typical of those found in molluscivorous fish. Pharyngeal teeth of the largest round gobies also showed considerable wear. Although changes in pharyngeal morphology may contribute to the previously described diet shift in round gobies as they age, genetic and environmental factors both likely influence pharyngeal remodeling and therefore merit further investigation.