An Experimental Investigation of Lime Juice Drying in a Pilot Plant Spray Dryer

One of the major problems in spray drying of fruit juices such as lime juice is stickiness and thermoplasticity of their compositions. Lime juice consists of invert sugars and citric acid, which have low glass transition temperatures. Due to this characteristic, the particles stick on the dryer wall upon their collision with it. As a result, drying of these materials is very difficult. In order to solve this problem, various percent of silicon dioxide and maltodextrin (DE5), based on total soluble solid content of lime juice, have been used to reach a suitable drying condition. A cool chamber wall spray dryer was used in this investigation in order to decrease the probability of particles stickiness on the wall. Our investigation revealed that an addition of 10% silicon dioxide and 20% maltodextrin (DE5) to lime juice is the optimum amount for a complete and successful drying of lime juice. Sampling of particles from different longitudinal distances in the dryer tower is carried out to find the particle moisture contents as they fly downward in the dryer. The results show a very fast decrease in entrance moisture contents. Based on our experimental data, the variation of moisture contents are presented as a function of radial distance from central line and longitudinal distance from the entrance region.     

Electrodeposition of catalytically active nickel powders from sulphate baths. I. Effect of bath constituents

A detailed study was made of the influence of the sulphate bath constituents: 0.3 - 0.0125 NiSO₄·7H₂O (I), 0.05 – 0.23 (NH₄)₂SO₄ (II), 0.1 – 0.4 H₃BO₃ (III) and 0.07 – 0.35 mol l^?1 Na₂SO₄·10H₂O (IV) on the electrodeposition of nickel powder. The cathodic polarization, current efficiency, growth morphology, crystallite size and catalytic activity of the electrodeposited nickel powders were affected to different extents by the bath constituents. A highly pure nickel powder characterized by a small crystallite size (776 Å) and moderate catalytic activity was obtained from a bath containing: 0.0125 (I), 0.23 (II), 0.1 (III) and 0.07 mol l^?1 (IV) at a current density of 10 A dm^?2 and electrolysis time 60 min. at 25 °C. Structural studies with a scanning electron microscope are given and a reaction mechanism for the electrolytic powder deposition is discussed.     

Polymerization of ethyl methacrylate,methyl methacrylate,and vinyl acetate using sulfonated polystyrene as the initiator

Polymerization of ethyl methacrylate (EMA) and methyl methacrylate (MMA) was achieved in glass dilatometers, at 86°C, using polystyrene sulfonate (Na⁺ and H⁺ forms) as initiators. The conversion of EMA to PEMA and MMA to PMMA increased with the time of polymerization, quantity of initiator, and size of dilatometer but decreased with volume of water. The polymer yield was higher for the Na⁺ than for the H⁺ form of the resin initiator. The average degree of polymerization increased with increase in the volume of water, but decreased with the quantity of initiator. Vinyl acetate could not be polymerized using either the Na⁺ or H⁺ forms of the polystyrene sulfonate as the initiator under the conditions of EMA or MMA polymerization.     

Toughening of vinylester–urethane hybrid resins through functionalized polymers

Liquid nitrile rubber, hyperbranched polyester, and core/shell rubber particles of various functionality, namely, vinyl, carboxyl, and epoxy, were added up to 20 wt % to a bisphenol‐A‐based vinylester–urethane hybrid (VEUH) resin to improve its toughness. The toughness was characterized by the fracture toughness (K_c) and energy (G_c) determined on compact tensile (CT) specimens at ambient temperature. Toughness improvement in VEUH was mostly achieved when the modifiers reacted with the secondary hydroxyl groups of the bismethacryloxy vinyl ester resin and with the isocyanate of the polyisocyanate compound, instead of participating in the free‐radical crosslinking via styrene copolymerization. Thus, incorporation of carboxyl‐terminated liquid nitrile rubber (CTBN) yielded the highest toughness upgrade with at least a 20 wt % modifier content. It was, however, accompanied by a reduction in both the stiffness and glass transition temperature (T_g) of the VEUH resin. Albeit functionalized (epoxy and vinyl, respectively) hyperbranched polymers were less efficient toughness modifiers than was CTBN, they showed no adverse effect on the stiffness and T_g. Use of core/shell modifiers did not result in toughness improvement. The above changes in the toughness response were traced to the morphology assessed by dynamic mechanical thermal analysis (DMTA) and fractographic inspection of the fracture surface of broken CT specimens. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 672–680, 2002; DOI 10.1002/app.10392     

Behavior of cellulose graft copolymer towards persulphate oxidation. III. Poly(acrylonitrile) graft copolymers

Cotton cellulose was graft copolymerized with poly(acrylonitrile) to different levels. The copolymers so obtained together with the nongrafted cellulose were oxidized at different pH's (4–10) and temperatures (50–70°C) with potassium persulphate. The oxidation reaction was studied with respect to oxygen consumption, mass loss, and changes in copper number and carboxyl content of the cellulosic materials. It was found that the rates of oxidation at pH 4 for the copolymers are substantially higher than that of the nongrafted cellulose and the rate of oxidation is higher the higher the level of grafting. The reverse is the case at pH 10. The mass loss increases as the oxygen consumption increases irrespective of the substrate used and the pH employed. The magnitude of the mass loss is substantially lower in the case of grafted cellulose than in the case of nongrafted cellulose. The cellulosic copolymers with higher graft levels show lower mass loss than those having lower graft levels. However, the copper number and carboxyl content of the oxidized grafted cellulose are higher than those of the nongrafted cellulose at the same oxygen consumption. It is believed that the presence of poly(acrylonitrile) graft in the molecular structure of cellulose impedes cellulosic chain scission without necessarily preventing oxidation of cellulose hydroxyls.     

Analysis of deformation processes in glassy polycarbonate using internal friction measurements during a tensile test

Internal friction has been measured by torsion at 1 Hz during tensile tests performed on glassy polycarbonate at room-temperature. Steady-state flow and transient effects have been studied during continuous tensile tests and strain-rate changes. During steady-state, internal friction and flow-stress vary in a similar way with strain-rate. But during transients, internal friction varies continuously while flow-stress passes through a maximum (or a minimum). These results are interpreted assuming that non-elastic deformation of glassy polymers requires some microscopic discontinuous processes such as motion of defects. Two parameters are considered: the velocity v and the density ρ of mobile defects. Assuming that the former is directly related to the flow stress, it has been shown that internal friction is related to the density of mobile defects ρ. This feature is used to interpret the different stages of a tensile test curve. Activation volumes for both velocity and density of mobile defects are calculated from experimental data.     

Effect of EFA deficiency on lipid transport from liver

Studies are reported of the effect of an essential fatty acid (EFA) deficiency on synthesis of triglycerides (TG) and phospholipids (PL) and secretion of these compounds by livers of male Sprague-Dawley rats. Animals were fed a semipurified diet containing corn oil or hydrogenated coconut oil (HCO) as the sole source of fat or no fat from weaning to 20 weeks of age. Liver function of the animals in each group was compared by an isolated liver perfusion technique with perfusates containing erythrocytes and linoleate, and in vivo experiments via tail vein injection of palmitate-³H. Perfusion experiments showed that an EFA deficiency reduced the ability of the liver to secrete TG and PL. Accumulation of TG in the liver and its diminished secretion into the blood of EFA deficient animals were demonstrated by in vivo experiments with palmitate-³H. The rate of conversion of linoleate to arachidonate and synthesis of PL was greater in livers of EFA deficient rats than in the control, corn oil fed animals. The results suggest a relationship of EFA metabolism to lipid transport. One of five papers to be published from the Symposium “Lipid Transport” presented at the AOCS Meeting, New Orleans, April 1970.     

Constrained regression in chemical engineering practice

Absolute equality constraints in multiple regression are shown to introduce only minor modifications in the normal equations by a subset of the regression parameters. It is essential that these are ordered such that the subset is observable through the constraints. The constraints are shown to give greater residuals about the regression, but the precision in the parameter estimation is improved.In general power function curve fitting, a quadratically convergent iterative computation of the optimal exponents uses the normal equations as equality constraints. The correlations between the coefficients and the exponents in a sum of power functions become very high, when the number of terms increases such that their individual observability is being greatly reduced. The effect is shown to be a very poor precision in the parameter estimation and a heavy oscillation in the coefficients.The algorithms suggested are illustrated by curve fitting of some binary equilibrium data, where the relative volatility model gives a superior fit to the data.     

Manufacture of Granulated Chitosan

Conditions for dry-wet spinning of spherical chitosan granules 0.5–2.0 mm in diameter into a two-layer spinning bath consisting of immiscible liquids are proposed, where an organic liquid, decane in particular, is the upper layer of the bath while a solution of ammonium hydroxide is the lower layer. The possibility of obtaining chitosan microgranules from 2 to 30 µm in diameter by emulsification of a solution of chitosan in decane or a solution of an anion-active surfactant — sodium dodecyl sulfate — is demonstrated. The effect of the molecular weight and concentration of the solutions on the granule-forming power of chitosan is established. A 6% solution of chitosan with a molecular weight of 200 kD is recommended for further studies.__________Translated from Khimicheskie Volokna, No. 5, pp. 26–29, January–February, 2005.     

Homogeneous Catalyzed Ozone Decomposition in the Presence of Co(II).

The homogeneous decomposition of ozone in the presence of a Co(II) catalyst has been investigated in aqueous solution. Under the conditions investigated (Co(II) concentration: 0.0 – 2.0?ppm, pH: 1.6- 8.4, O₃ concentration: 5 10^?5 – 2.0 10⁴?M) the process can be assumed to follow pseudo first order kinetics with respect to ozone. Cobalt concentration dependency also obeys first order kinetics although it may be considered to reach a steady state concentration. pH exerts a positive influence on the decomposition rate from 1.6 to 7.1, the process leveling off at pH 8.4. An Arrhenius analysis of the temperature effect gave a moderate activation energy of the global reaction (E=10917?cal mol^?1). A more detailed radical mechanism than a simple pseudo first order reaction can be postulated for simulation purposes. By numerical optimization of some unknown kinetic constants the influence of several operating variables can be adequately predicted.