Exploring aspects of cell intelligence with artificial reaction networks

The Artificial Reaction Network (ARN) is a Cell Signalling Network inspired connectionist representation belonging to the branch of A-Life known as Artificial Chemistry. Its purpose is to represent chemical circuitry and to explore computational properties responsible for generating emergent high-level behaviour associated with cells. In this paper, the computational mechanisms involved in pattern recognition and spatio-temporal pattern generation are examined in robotic control tasks. The results show that the ARN has application in limbed robotic control and computational functionality in common with Artificial Neural Networks. Like spiking neural models, the ARN can combine pattern recognition and complex temporal control functionality in a single network, however it offers increased flexibility. Furthermore, the results illustrate parallels between emergent neural and cell intelligence.     

Decolourisation of aqueous dyes by sequential oxidation treatment with ozone and Fenton's reagent

Combined oxidation with ozone and Fenton's reagent (‘Fentozone’ process) for decolourisation of aqueous dyes was studied and compared with traditional Fenton's reagent. Although the ‘Fentozone’ process was found to be effective at a wide range of pH values, the maximum colour removal was achieved at pH 4. The effect of pre‐ozonation on colour removal efficiency of aqueous dyestuffs in the subsequent treatment with Fenton's reagent was investigated. The reaction kinetics using water‐soluble acid and reactive dyes were also studied. Our experimental results show that pre‐ozonation can considerably accelerate decomposition of dyestuffs in the subsequent treatment with Fenton's reagent. Different concentrations of ferrous sulfate were used to investigate their influences on the removal of colour. The rate of reaction increased with increasing doses of ferrous sulfate. © 2002 Society of Chemical Industry     

Albumin stimulates lysophosphatidic acid acyltransferase activity in T-lymphocyte membranes

Phosphatidic acid (PtdOH) and lysophosphatidic acid (lysoPtdOH) have been shown to enhance T-lymphocyte function. However, the FA preference and influence of acyl-CoA binding proteins on lysoPtdOH and PtdOH biosynthesis are not known. Therefore, we determined glycerol-3-phosphate acyltransferase (GPAT) and lysophosphatidic acid acyltransferase (LAT) activity in rat T-lymphocyte and liver membrane preparations in the presence of palmitoyl-CoA and oleoyl-CoA with or without BSA. We found two different properties of GPAT and LAT in whole T-lymphocyte membrane preparations relative to liver. First, T-lymphocyte basal GPAT and LAT activities were similar, whereas in liver membranes LAT activity was 10-fold higher than GPAT. Second, T-lymphocyte LAT, but not GPAT, activity was inducible (fivefold) by the addition of albumin in the presence of palmitoyl-CoA but not oleoyl-CoA. In contrast, albumin stimulated GPAT, but not LAT, activity in liver membranes in the presence of palmitoyl-CoA. These results show, for the first time, that T-lymphocyte LAT activity can be increased by the presence of an acyl-CoA binding protein, which may indicate a new important control mechanism for regulating intracellular lysoPtdOH and PtdOH levels in T-lymphocytes.     

Development of a comprehensive free radical photopolymerization model incorporating heat and mass transfer effects in thick films

A comprehensive kinetic model describing photopolymerization is developed which allows variation of temperature, species concentrations, and light intensity through the thickness of a photopolymerized film. Heat and mass transfer effects are included, as is the generation of heat by both reaction and light absorption. In addition to initiation, propagation, and termination mechanisms, both primary radical termination and inhibition are incorporated into the model. The possible presence and diffusion of an inert solvent are also accounted for. Thus, the model is useful for examining complex polymerization kinetics and behavior in industrially and commercially important thick film photopolymerizations, such as the curing of contact lenses, dental restorative materials, photolithographic resists, and optoelectronic coatings. The comprehensive model is used to predict polymerization rate, temperature, and conversion profiles in a variety of systems. The effects of heat generation and the thermal boundary conditions are explored, with the result that heat generation in thick samples leads to greatly increased conversions approaching 100 percent. Increased temperature in these samples also may lead to the appearance of two rate maxima, with the first due to the temperature increase and the second caused by the autoacceleration process. The magnitude of the temperature increase, along with the resultant effects, is more pronounced in insulated systems.     

Consolidation Behavior of Flocculated Alumina Suspensions

The consolidation behavior of flocculated alumina suspensions has been analyzed as a function of the interparticle energy. Consolidation was performed by a centrifugal force field or by gravity, and both the time-dependent and equilibrium density profiles were measured by a gamma-ray absorption technique. The interparicle energy at contact was controlled by adsorbing fatty acids of varying molecular weight at the alumina/decalin interface. We found that strongly attractive interactions result in a particle network which resists consolidation and shows compressible behavior over a large stress range. The most weakly flocculated suspension showed an essentially incompressible, homogeneous density profile after consolidation at different centrifugal speeds. We also found a significant variation in the maximum volume fraction, φ_m, obtained, with φ_m∼ 0.54 for the most strongly flocculated suspension to φ_m∼ 0.63 for the most weakly flocculated suspension. The compresive yield stresses show a behavior which can be fitted to a modified power law. In this paper, we discuss possible correlations between the fitting parameters and physical properties of the flocculated suspensions.     

Water uptake and tensile properties of carboxylated styrene butadiene rubber based water born paints: Models for water uptake prediction

Despite significant advances in water based surface coating technology, the presence of surfactants in emulsion polymer binders leads to loss of performance after prolonged immersion in water, relative to solvent based coatings that are free of surfactant impurities. This study begins with water uptake evaluation of a range of emulsion polymer binders. A carboxylated styrene butadiene rubber latex (c-SBR) performed best in the latter evaluations and was selected for the formulation of an exterior grade paint and construction of a mathematical model to predict water uptake of the dry film. The c-SBR was then compounded with a range of inorganic fillers and water uptake and tensile properties were evaluated. Talc was found to be the best performing filler, and was used in a three factorial central composite design study where the simultaneous effects of talc, titanium dioxide and phenolic stabiliser on water up take were evaluated and fitted to response equations. A quadratic model was found to provide the most accurate prediction of effects associated with interactions between talc and TiO₂. Certain combinations of talc and titanium dioxide were found to be synergistic in reducing the water uptake. This was considered to be associated with a packing effect stemming from the vast difference in particle size between talc and titanium dioxide particles. An optimised formulation was finally prepared to meet one of the final formulation objectives; i.e., minimised water uptake. Preparation of such a formulation showed that the predicted and measured water uptake responses were in excellent agreement. This study illustrates the effectiveness of statistical experimental design methods in predicting the water uptake characteristics of water-based coatings.     

Drag reduction characteristics of graft copolymers prepared by the gamma irradiation of poly(oxyethylene) in the presence of acrylic acid

Graft copolymers were prepared by irradiation of poly(oxyethylene), PEO, aqueous solutions in presence of acrylic acid. Chain transfer to PEO controls the graft length, the measured chain transfer constant of the acrylic acid radicals to PEO being 4.11 × 10^?4 at 25°C. The drag reduction characteristics of the graft copolymers were measured in the Reynolds number range 10⁴–10⁵ in a smooth-walled tube, 0.635 cm inside diameter. The drag reduction falls to near zero as the solution pH is lowered to 3, evidence of the formation of a PEO-poly(acrylic acid) coacervate.     

Glass Furnace Boost Technology-Series/Parallel Switch

In the paper, the characters and fields were introduced for utilizing the Series/Parallel Switch (SPS). The circuit principle of the SPS technology was analyzed in detailed, explained and illuminated. We understood clearly the difference between SPS and single-phase transformator by the figure and table. Finally, it summarized that the main characters of SPS.     

Adaptive relationships of epoxide hydrolase in herbivorous arthropods

Epoxide hydrolase catalyzes a simple hydrolysis of reactive cyclic ethers that may otherwise alkylate and impair critical proteins and nucleic acids required for life. Although much less studied than the cytochrome P-450 monooxygenases that produce epoxides, differences in subcellular, tissue, pH, substrate, and inhibitor specificities argue for at least three forms of insect epoxide hydrolase. Increasing numbers of epoxides are being identified as plant allelochemicals, antifeedants, and essential hormones or precursors for herbivorous arthropods, and in many cases an associated alkene to diol pathway of metabolism is found. A role for epoxide hydrolase in arthropod-plant interactions is strongly supported by species comparisons and by age-activity and induction studies. Two major limitations for study in biochemical ecology of epoxide hydrolase are the lack of an effective in vivo inhibitor and a range of commercially available radiolabeled substrates for the enzymes.     

Hydrogenation of 3,4-epoxy-1-butene over Cu–Pd/SiO2 catalysts prepared by electroless deposition

Electroless deposition has been used to prepare Cu–Pd/SiO₂ bimetallic catalysts wherein initial Cu coverages are limited only to the pre-existing Pd surface. Cu loading on the Pd surface can be systematically varied by modification of deposition kinetic parameters. In this case deposition time was used as the kinetic variable for the preparation of a series of Cu–Pd catalysts. These materials have been characterized using atomic absorption, CO chemisorption, and FT-IR (adsorption of CO), and then evaluated for the hydrogenation of 3,4-epoxy-1-butene, a functionalized olefin having many potential reaction pathways. Catalyst performance and characterization results suggest that Cu is not distributed in a monodisperse manner on the Pd surface, indicating the existence of autocatalytic deposition of Cu on Cu sites. The FT-IR results suggest that although CO adsorption on all sites is suppressed by Cu addition, initial Cu deposition occurs more readily on certain sites. The bimetallic Cu–Pd sites that are formed exhibit unusually high activity for EpB conversion and formation of unsaturated alcohols and aldehydes. This bimetallic effect on catalyst activity and selectivity is best explained, not by the existence of either ligand or ensemble effects, but rather by the bifunctional nature of the Cu–Pd sites present on the surface of these catalysts.