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Kinetics Parameters (kinetics + parameter)
Selected AbstractsBDNF, NT-3 and NGF induce distinct new Ca2+ channel synthesis in developing hippocampal neuronsEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 11 2000Pietro Baldelli Abstract Neurotrophins exert short- and long-term effects on synaptic transmission. The mechanism underlying these forms of synaptic plasticity is unknown although it is likely that intracellular Ca2+ and presynaptic Ca2+ channels play a critical role. Here we show that BDNF, NGF and NT-3 (10,100 ng/mL) exhibit a selective long-term up-regulation of voltage-gated Ca2+ current densities in developing hippocampal neurons of 6,20 days in culture. NGF and NT-3 appear more effective in up-regulating L-currents, while BDNF predominantly acts on non-L-currents (N, P/Q and R). The effects of the three neurotrophins were time- and dose-dependent. The EC50 was comparable for BDNF, NGF and NT-3 (10,16 ng/mL) while the time of half-maximal activation was significantly longer for NGF compared to BDNF (58 vs. 25 h). Despite the increased Ca2+ current density, the neurotrophins did not alter the voltage-dependence of channel activation, the kinetics parameters or the elementary properties of Ca2+ channels (single-channel conductance, probability of opening and mean open time). Neurotrophin effects were completely abolished by coincubation with the nonspecific Trk-receptor inhibitor K252a, the protein synthesis blocker anisomycin and the MAP-kinase inhibitor PD98059, while cotreatment with the PLC-, blocker, U73122, was without effect. Immunocytochemistry and Western blotting revealed that neurotrophins induced an increased MAP-kinase phosphorylation and its translocation to the nucleus. The present findings suggest that on a long time scale different neurotrophins can selectively up-regulate different Ca2+ channels. The action is mediated by Trk-receptors/MAP-kinase pathways and induces an increased density of newly available Ca2+ channels with unaltered gating activity. [source] Curing behavior of a novel polytriazole resinJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007Liqiang Wan Abstract The curing behavior of a novel low temperature curing polytriazole resin, prepared from p -xylylene diazide and N,N,N,,N, -tetrapropargyl- p,p, -diaminodiphenylmethane, was investigated by DSC and rheological analyses. The kinetics of the curing of the resin was studied by nonisothermal and isothermal DSC measurements and the kinetics parameters were obtained. The values of apparent activation energy Ea of the curing reaction obtained by nonisothermal and isothermal DSC are 80.7 and 75.3 kJ/mol, respectively. The curing of the resin was traced by the isothermal rheological analysis. The gelation times of the resin at 70, 75, 80, and 85°C are about 200, 150, 110, and 75 min, respectively. The viscosity equation for the resin was found as follows: © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Effect of phosphate fertilization on crop yield and soil phosphorus status,JOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, Issue 5 2003Anne Gallet Abstract To evaluate the effect of three phosphorus (P) fertilization regimes (no P, P input equivalent to P off-take by crops, P input higher than P off-take) on crop yield, P uptake, and soil P availability, seven field experiments (six in crop rotations, one under permanent grassland) were conducted in Switzerland during nine years (six trials) or 27 years (one trial). Soil total P (Pt), inorganic P (Pi), organic P (Po), and the amount of isotopically exchangeable soil P were measured in the 0,20,cm and 30,50,cm layers of the arable soils and in the 0,10,cm layer of the permanent grassland soil. Omitting P fertilization resulted in significant yield decreases only in one field crop trial as the amount of P isotopically exchangeable within one minute (E1min) reached values lower than 5 mg P (kg soil),1. In the absence of P fertilization Pi decreased on average from 470 to 410 mg P (kg soil),1 in the upper horizon of 6 sites while Po decreased only at two sites (from 510 to 466 mg P (kg soil),1 on average). In all the treatments of the trials started in 1989 the E1min values of the upper horizon decreased on average from 15.6 to 7.4 mg P (kg soil),1 between 1989 and 1998. These decreases were also observed when P inputs were higher than crops needs, showing that in these soils the highest P inputs were not sufficient to maintain the high initial available P levels. Finally for the six arable trials the values of the isotopic exchange kinetics parameters (R/r1, n, CP) and P exchangeable within 1 minute (E1min) at the end of the experiment could be estimated from the values measured at the beginning of trial and the cumulated P balance. Der Einfluss der Phosphordüngung auf den Pflanzenertrag und den Phosphorstatus des Bodens Die Begrenzung der Düngung mit Phosphat (P) bei Böden, die bereits hohe Gehalte an verfügbarem P aufweisen, kann zur Verringerung der P-Verluste in Oberflächen- und Grundwasser beitragen. Sieben Feldversuche (6 Versuche mit Ackerkulturen, 1 Versuch mit Dauerwiese) wurden während 9 Jahren (6 Versuche) resp. 27 Jahren (1 Versuch) durchgeführt mit dem Ziel, den Einfluss von drei Düngungsraten (keine P-Gabe, P-Gabe entsprechend dem P-Entzug durch die Pflanzen und P-Gabe höher als der P-Entzug durch die Pflanzen) auf Pflanzenertrag, P-Aufnahme und P-Verfügbarkeit zu studieren. Die Gehalte an anorganischem P (Pi) und organischem P (Po), sowie deren Summe (Pt) und die Gehalte an isotopisch austauschbarem P wurden in den Bodentiefen von 0,20,cm und 30,50,cm der ackerbaulichen Versuche und in einer Bodentiefe von 0,10,cm in der Dauerwiese gemessen. Der Verzicht auf P-Düngung führte nur in einem der ackerbaulichen Versuche zu einer signifikanten Abnahme des Pflanzenertrags, wobei der Gehalt an isotopisch austauschbarem P (E1min) unter 5 mg P (kg Boden),1 fiel. Pi sank bei Verzicht auf P-Düngung im oberen Horizont von 6 Böden durchschnittlich von 470 auf 410 mg P (kg Boden),1, während Po nur in 2 Böden absank (durchschnittlich von 510 auf 466 mg P (kg Boden),1). Ueber alle Düngungsverfahren jener Versuche, die 1989 begonnen hatten, sank E1min im oberen Horizont von 1989 bis 1998 durchschnittlich von 15.6 auf 7.4 mg P (kg Boden),1. Die Abnahme wurde auch beobachtet, wenn die P-Gabe höher war als der P-Entzug durch die Pflanzen, was zeigt, dass in diesen Böden selbst die höchste P-Gabe nicht genügte, um den ursprünglich hohen Gehalt an verfügbarem P aufrecht zu erhalten. Schließlich wurden in den 6 ackerbaulichen Versuchen die Parameter der Isotopenaustauschkinetik (R/r1, n, CP) und E1min am Ende des Versuches mit den ursprünglichen Werten zu Beginn des Versuchs verglichen. Es ergaben sich signifikante Beziehungen zwischen den Werten am Ende des Versuchs einerseits und den ursprünglichen Werten und der P-Bilanz andererseits. [source] Afterglow and thermally stimulated luminescence induced by UV radiation in CVD diamondPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 9 2007M. Barboza-Flores Abstract Afterglow (AG) and thermoluminescence (TL) of CVD diamond UV-irradiated with wavelength of 200,260 nm at room temperature are reported. The AG curves monotonously decrease with time and are fitted well by the hyperbolic law. The decay times depends on UV wavelength and decreases with the AG intensity increasing. The TL glow curves exhibit two pronounced TL peaks with maxima at about 350 K and 513 K with unstructured signal between them and are fitted well by four TL peaks. The first, 350 K peak with the activation energy of 0.59 eV was supposed to be second kinetics order. The higher temperature peaks at 402 K, 445 K and 513 K with the activation energies of 0.46 eV, 0.49 eV and 0.68 eV, respectively were assumed to be first kinetics order. The comparison of the AG decay times with the kinetics parameters of the 350 K TL peak proved that AG is caused by thermal emptying of the traps responsible for the 350 K peak. The behaviour of AG and 350 K TL peak was described by the model, in which shallow traps, recombination centers and deep thermally disconnected traps are taken into account. The AG and TL creation spectra are practically the same and consists of a broad band, which exponentially increases from 260 nm, reaches a maximum at 240 nm and then begins decreasing. The creation spectra of the AG and TL peaks are the same and closely related with the fundamental absorption of UV light near indirect band gap of diamond. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Kinetics and thermodynamics of isothermal curing reaction of epoxy-4, 4,-diaminoazobenzene reinforced with nanosilica and nanoclay particlesPOLYMER COMPOSITES, Issue 8 2010M. Barghamadi The kinetics of the cure reaction for a system of bisphenol-A epoxy resin (DGEBA), with 4, 4,-diaminoazobenzene (DAAB), reinforced with nanosilica (NS), and nanoclay (NC) by means of isothermal technique of differential scanning calorimetry were studied. The Kamal autocatalytic-like kinetic model was used to estimate the reaction orders (m, n), rate constants (k1, k2), and also active energies (Ea) and pre-exponential factors (A) of the curing reaction. However, the existence of NS and NC with hydroxyl groups in the structure improves the cure reaction and influence the rate of reaction and therefore kinetics parameters. The Ea of cure reaction of DGEBA/DAAB system showed a decrease when nanoparticles were present and therefore the rate of the reaction was increased. Using the rate constants from the kinetic analysis and transition state theory, thermodynamic parameters such as enthalpy (,H#), entropy (,S#), and Gibbs free energy (,G#) changes were also calculated. The thermodynamic functions were shown to be very sensitive parameters for evaluation of the cure reaction. POLYM. COMPOS., 31:1442,1448, 2010. © 2009 Society of Plastics Engineers [source] Optimization of cure kinetics parameter estimation for structural reaction injection molding/resin transfer moldingPOLYMER COMPOSITES, Issue 6 2001Robert J. Duh A numerical method is proposed for polymer kinetic parameter estimation of either Structural Reaction Injection Molding (SRIM) or Resin Transfer Molding (RTM). The method simulates either radial flow or axial flow of reactive resins through a fiber preform inside a mold cavity. This method considers a non-isothermal environment with different inlet boundary conditions. Based on the molding conditions, this method can find the best values of chemical kinetic parameters by comparing the simulated temperature history and the experimental temperature history. Since the kinetic parameters are estimated with the real molding conditions, the simulations using these parameter values can have better agreement with molding data than those parameters which are obtained from idealized conditions such as Differential Scanning Calorimeter (DSC). The optimization approach was verified by estimating kinetics parameters for RTM data available in the literature. Temperatures predicted by the optimized kinetics parameters are compared with experimental data for two different molding conditions: injection of a thermally activated resin into a radial mold under constant pressure flow, and injection of a mix activated resin into a radial mold under constant volume. In both cases, the optimized kinetics parameters fit the temperature data well. [source] Epoxy nanocomposites: Analysis and kinetics of curePOLYMER ENGINEERING & SCIENCE, Issue 6 2004M.-T. Ton-That The effect of organo-nanoclay (Nanomer I30E) on the cure mechanism and kinetics of epoxy nanocomposites based on Epon 828 and Epicure 3046 was studied by means of dynamic differential scanning calorimetry (DSC) at four heating rates (2.5, 5, 10, and 20°C·min,1) and by Fourier transform infrared (FT-IR) spectroscopy. The DSC cure data for epoxy-amine mixtures with and without nanoclay was modeled by means of different approaches; the Kissinger and isoconversional models were used to calculate the kinetics parameters while the Avrami model was utilized to compare the cure behavior of the two systems. The Nanomer I30E was shown to initiate rapid homopolymerization of the Epon 828 resin at temperatures above 180°C. For the epoxy-amine mixtures, the presence of nanoclay had little effect on the cure kinetics in the early stages (i.e., at lower temperatures), and the apparent activation energy was around 60 kJ·mol,1. However, in the later stages, the apparent activation energy increased significantly in the absence of nanoclay, but did not do so when it was present. The presence of nanoclay also lowered the final glass transition temperature by about 4°C. Polym. Eng. Sci. 44:1132,1141, 2004. © 2004 Society of Plastics Engineers. [source] An alternative model for predicting the cure kinetics of a high temperature cure epoxy adhesive,POLYMER ENGINEERING & SCIENCE, Issue 1 2003Angela D. Rogers The purpose of this work was to develop a cure kinetics model for a commercially available high temperature cure epoxy adhesive commonly used in the aerospace industry. While there are several phenomenological cure kinetic models commonly used in the literature for describing the rate of conversion of thermosetting epoxy adhesives as a function of degree of conversion, none of these models adequately depicts the adhesive used in this work over the entire range of conversion. Hence, by curve fitting empirical data collected using differential scanning calorimetry and refinement of existing models, an alternative model is proposed. The form of the present model suggests that chemical curing is the result of the combination of two autocatalytic reactions. The model is able to account for both the chemically controlled and diffusion controlled regimes of the cure. This paper also describes a novel iterative approach for predicting kinetics parameters as a function of isothermal cure temperature. Excellent agreement between experimental measurements and model predictions has been demonstrated over the entire range of conversion. [source] | ||||||||||