Kinetics of Rubber-Modified Nylon 6

2014 ◽  
Vol 887-888 ◽  
pp. 951-954
Author(s):  
Hong Kai Zhao ◽  
Hong Li Wang
Keyword(s):  
Activation Energy ◽  
Reaction Order ◽  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Exponential Factor ◽  
First Order ◽  
Adiabatic Approach ◽  
Research Findings ◽  
Styrene Butadiene ◽  
Kinetics Of

Kinetic parameters are calculated based on the reactive temperature rise curve measured by adiabatic approach at the temperature of 145 to 160 °C with the catalytic system of NaOH and acyl caprolactam End-capped butadiene-acrylonitrile rubber (CHTBN) or styrene-butadiene rubber (CHTBS). The reaction order is first order, the activation energy is between 72.91−73.16 kJ∙mol−1 and the pre-exponential factor is between 3.22×1011− 3.38×1011 mol1−n∙s−1 in the system of CHTBN/NaOH. While in CHTBS/NaOH, the reaction order is between 1.23-1.34, the activation energy is between 85.55－86.88 kJ∙mol−1 and the pre-exponential factor is between 4.52×1011−5.0 9×1011 mol1−n∙s−1. The adiabatic reaction kinetic model of caprolactam anion was constructed based on the existing research findings, by which the polymerizing reaction is simulated. The coincidence between the simulation results and the experimental data revealed that the model is reasonable and correct.

Research on the Kinetics of Nylon Polymerized by Caprolactam Anionic Polymerization Using Adiabatic Method

2014 ◽  
Vol 887-888 ◽  
pp. 955-959 ◽  
Author(s):  
Hong Kai Zhao ◽  
Hong Li Wang
Keyword(s):  
Anionic Polymerization ◽  
Reaction Kinetic ◽  
Reaction Order ◽  
Reaction Heat ◽  
Exponential Factor ◽  
Reaction Systems ◽  
First Order ◽  
Research Findings ◽  
Simulation Results ◽  
Kinetics Of

Kinetic parameters were calculated based on the catalytic reaction systems of sodium caprolactam salt、N-75 biuret and at the temperature of 145 to 160 °C. The reaction order was approximately first order. The activation energy was between 73.2−77.1 kJ∙mol−1 and the pre-exponential factor was between 2.9×1011−3.6×1011 mol1−n∙s−1. The calculated reaction heat of 134.5−137.3 J∙g−1 was in consonance with the literature value of 138.6 J∙g−1. The adiabatic reaction kinetic model of caprolactam anion was constructed based on the existing research findings. The coincidence between the simulation results and the experimental data revealed that the model was reasonable and correct.

Kinetics and Activation Parameters for the Alkaline Aqueous Rearrangement of Trichorfon [O,O-Dimethyl-(2,2,2-Trichloro-1-Hydroxyethyl) Phosphonate] to Dichlorvos [O,O-Dimethyl-O-(2,2-Dichloroethenyl)Phosphate]

2001 ◽  
Vol 36 (3) ◽  
pp. 589-604 ◽  
Author(s):  
Julian M. Dust ◽  
Christopher S. Warren
Keyword(s):  
Activation Energy ◽  
High Pressure ◽  
Activation Parameters ◽  
Base Catalysis ◽  
Rearrangement Product ◽  
Exponential Factor ◽  
First Order ◽  
Pseudo First Order ◽  
Order Plot ◽  
Kinetics Of

Abstract The kinetics of the alkaline rearrangement of O,O-dimethyl-(2,2,2-trichloro-1- hydroxyethyl)phosphonate, (trichlorfon, 1), the active insecticidal component in such formulations as Dylox, was followed at 25±0.5°C by high pressure liquid chromatography (UV-vis detector, 210 nm). The rearrangement product, O,Odimethyl- O-(2,2-dichloroethenyl)phosphate (dichlorovos, 2), which is a more potent biocide than trichlorfon, undergoes further reaction, and the kinetics, consequently, cannot be treated by a standard pseudo-first-order plot. A two-point van't Hoff (initial rates) method was used to obtain pseudo-first-order rate constants (kѱ) at 25, 35 and 45°C: 2.6 × 10-6, 7.4 × 10-6 and 2.5 × 10-5 s-1, respectively. Arrhenius treatment of this data gave an activation energy (Ea) of 88 kJ·mol-1 with a pre-exponential factor (A) of 5.5 × 109 s-1. Kinetic trials at pH 8.0 using phosphate and tris buffer systems show no buffer catalysis in this reaction and indicate that the rearrangement is subject to specific base catalysis. Estimates are reported for pseudo-first-order half-lives for trichlorfon at pH 8.0 for environmental conditions in aqueous systems in the Corner Brook region of western Newfoundland, part of the site of a recent trichlorfon aerial spray program.

Studies on Dicumyl Peroxide Vulcanization of Styrene—Butadiene Rubber in Presence of Sulfur and 2-Mercaptobenzothiazole

1974 ◽  
Vol 47 (2) ◽  
pp. 266-281 ◽  
Author(s):  
C. K. Das ◽  
S. Banerjee
Keyword(s):  
Zinc Oxide ◽  
Stearic Acid ◽  
Crosslink Density ◽  
Addition Reaction ◽  
Styrene Butadiene Rubber ◽  
Methyl Groups ◽  
Butadiene Rubber ◽  
First Order ◽  
First Order Kinetics ◽  
Styrene Butadiene

Abstract The effect of sulfur, MBT, zinc oxide, and stearic acid on the DCP vulcanization of SBR has been studied. DCP decomposition obeys first order kinetics in all cases, but its rate constant is higher in presence of MBT. Sulfur and MBT reduce the crosslink density due to DCP. In the mixes containing sulfur, MBT, zinc oxide, and stearic acid in presence of DCP the crosslink density is initially additive. Here oxidation of some pendent vinyl groups are effected by DCP, and these groups also take part in thiol addition reaction with MBT. The thiazole accelerated sulfuration of SBR proceeds fundamentally by the same mechanism as reported for NR, but the details show slight difference chiefly due to the presence of pendent vinyl groups and styrene units in the chain and due to the absence of pendent methyl groups in SBR.

Vulcanization kinetics of nano-silica filled styrene butadiene rubber

Polymer ◽  
2014 ◽  
Vol 55 (24) ◽  
pp. 6426-6434 ◽  
Author(s):  
Seyed Mostaffa Hosseini ◽  
Mehdi Razzaghi-Kashani
Keyword(s):  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Nano Silica ◽  
Vulcanization Kinetics ◽  
Styrene Butadiene ◽  
Kinetics Of

scholarly journals Kinetics of the Carbon Monoxide Oxidation Reaction Under Microwave Heating

1996 ◽  
Vol 430 ◽  
Author(s):  
W. Lee Perry ◽  
Joel D. Katz ◽  
Daniel Rees ◽  
Mark T. Paffett ◽  
Abhaya Datye
Keyword(s):  
Activation Energy ◽  
Carbon Monoxide ◽  
Co Oxidation ◽  
Microwave Heating ◽  
Oxidation Reaction ◽  
Reaction Order ◽  
Thermal Gradients ◽  
Exponential Factor ◽  
Co Oxidation Reaction ◽  
Kinetics Of

Abstract915 MHz microwave heating has been used to drive the CO oxidation reaction over Pd/Al2O3 without significantly affecting the reaction kinetics. As compared to an identical conventionally heated system, the activation energy, pre-exponential factor, and reaction order with respect to CO were unchanged. Temperature was measured using a thermocouple extrapolation technique. Microwave-induced thermal gradients were found to play a significant role in kinetic observations.

THE THERMAL DECOMPOSITION OF STYRENE–BUTADIENE POPCORN POLYMER

1950 ◽  
Vol 28b (1) ◽  
pp. 5-16
Author(s):  
C. A. Winkler ◽  
J. Halpern
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Linear Relation ◽  
Frequency Factor ◽  
Thermal Reaction ◽  
Cross Linking ◽  
First Order ◽  
Bond Scission ◽  
Styrene Butadiene ◽  
Kinetics Of

At temperatures of the order of 250 °C., popcorn polymer undergoes decomposition to soluble polymer. The reaction is catalyzed by peroxides present in the popcorn when the latter is formed. These peroxides may be removed by extracting the polymer with benzene. The kinetics of both the catalyzed and purely thermal solubilization reactions were investigated. The rates of both reactions are first order, the catalyzed degradation having a higher activation energy and a higher frequency factor. The rate of the thermal reaction decreases and its activation energy increases with increasing butadiene content of the polymer. A linear relation between the activation energy and the log of the frequency factor, for the decomposition of popcorn polymers of different butadiene contents, was observed. The results indicate that the rate of solubilization is determined by the activation energy of the bond scission process, and is independent of the degree of cross-linking of the polymer.

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