共查询到20条相似文献,搜索用时 31 毫秒
1.
Itzhak Knigsberg Joseph Jagur-Grodzinski 《Journal of polymer science. Part A, Polymer chemistry》1983,21(8):2535-2546
The decomposition of polybromostyryl carbanions (PBS?), obtained by anionic polymerization of 4-bromostyrene in tetrahydrofuran (THF), was investigated in the dark in a temperature range of ?6–?21°C. It was accompanied by the evolution of bromine anions and by the formation of polymeric allylic carbanions (λmax = 575 nm; εmax = 6800 eq?1·L·cm?1). The reaction mechanism was elucidated. The rate constant of the unimolecular rate-determining step of the process was 1.3 × 10?5 s?1 and 9.7 × 10?5 s?1 at ?21 and ?6°C, respectively. Its apparent energy of activation Eapp = 18.38 Kcal/mol. The polybromostyrenes with allylic carbanions at their ends may decompose further. Their “dark” decomposition yielded 1,3-butadiene-1,3-diphenyl-macromers. The mechanisms of decomposition of the PBS? carbanions and the dark decomposition of the polybromostyryl allylic carbanions are analogous. The rate constant of the latter process was 2.5 × 10?6 s?1 at ?6°C. The anionic polymerization of prepared macromers can be initiated in THF at ?78°C by α-methylstyryl carbanions, which do not react, however, with PBS? carbanions. “Comblike” polymacromers were prepared in which each branch had a molecular weight of about 50,000. The overall molecular weight of the polymacromer was estimated to be about 1 × 106. It has been assumed that the 2–1 mode of addition to the diene group of the macromer is predominant during its polymerization. The 3–4 mode of addition followed by proton shift represents the termination step. The 4–3 mode of addition was ruled out on the basis of spectroscopic evidence. 相似文献
2.
E. A. S. Cavell I. T. Gilson 《Journal of polymer science. Part A, Polymer chemistry》1966,4(3):541-550
The initiation of the polymerization of acrylamide by 4-4′-dicyano-4-4′-azopentanoic acid in aqueous solution has been studied kinetically at 25°C. Ferric chloride and ferric sulfate were used to terminate polymerization so that rates of initiation could be calculated from the rates of production of ferrous iron. Velocity coefficients at 25°C. for the initiation reaction were found to be (25.7 ± 2.8) × 10?7 sec.?1 for the ferric chloride terminated reaction and (73.6 ± 0.6) × 10?7 sec.?1 for the ferric sulfate-terminated polymerization. The value reported for the initiation reaction when acrylamide is polymerized in the absence of metal salts is 1.29 × 10?7 sec.?1. Velocity coefficients for the termination reaction have been calculated from the overall rates of polymerization obtained with ferric salts present. In the case of the ferric chloride-terminated reaction, it has been shown that the rate of polymerization is reduced by increasing the total concentration of chloride ions. Termination velocity coefficients at 25°C. for the inner sphere complexes FeCl2+·5H2O and FeSO4+·4H2O have been calculated to be 18.9 × 104 and 7.98 × 104 l./mole-sec., respectively. The dependence on the concentration of ferric chloride of the molecular weights of the polymers produced has also been considered. 相似文献
3.
Valérie Sciannamea Jean‐Marie Catala Robert Jérôme Christophe Detrembleur 《Journal of polymer science. Part A, Polymer chemistry》2007,45(7):1219-1235
Kinetics of the free radical polymerization of styrene at 110 °C has been investigated in the presence of C‐phenyl‐N‐tert‐butylnitrone (PBN) and 2,2′‐azobis(isobutyronitrile) (AIBN) after prereaction in toluene at 85 °C. The effect of the prereaction time and the PBN/AIBN molar ratio on the in situ formation of nitroxides and alkoxyamines (at 85 °C), and ultimately on the control of the styrene polymerization at 110 °C, has been investigated. As a rule, the styrene radical polymerization is controlled, and the mechanism is one of the classical nitroxide‐mediated polymerization. Only one type of nitroxide (low‐molecular‐mass nitroxide) is formed whatever the prereaction conditions at 85 °C, and the equilibrium constant (K) between active and dormant species is 8.7 × 10?10 mol L?1 at 110 °C. At this temperature, the dissociation rate constant (kd) is 3.7 × 10?3 s?1, the recombination rate constant (kc) is 4.3 × 106 L mol?1 s?1, whereas the activation energy (Ea,diss.), for the dissociation of the alkoxyamine at the chain‐end is ~125 kJ mol?1. Importantly, the propagation rate at 110 °C, which does not change significantly with the prereaction time and the PBN/AIBN molar ratio at 85 °C, is higher than that for the thermal polymerization at 110 °C. This propagation rate directly depends on the equilibrium constant K and on the alkoxyamine and nitroxide concentrations, as well. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1219–1235, 2007 相似文献
4.
J. T. Guthrie L. J. Squires 《Journal of polymer science. Part A, Polymer chemistry》1984,22(1):135-144
The effect of a range of 10 organic nitriles on the radiation-induced polymerization of styrene was studied. A dose rate of 4.4 rad s?1 was used. A rate of polymerization of styrene (1.744 mol L?1 of toluene solution) of 5.0 × 10?7 mol L?1 s?1 was found. With organic nitriles present (styrene:nitrile ratio of 1:0.28) the rate of polymerization increased. Rates in the range of 5.5 × 10?7 ?5.2 × 10?6 mol L?1 s?1, depending on the nitrile present, were obtained. The polymers were partially characterized and evidence of involvement of each of the nitriles in the polymer chains was revealed. The increase in rate of polymerization has been attributed to the part played by nitrile radicals in the initiation of styrene polymerization. Radical yield values [as G(nitrile radical)] were derived from the relevant rate expressions. Values ranged from 2.7 to 49.5, depending on the particular nitrile. Corresponding values of G(nitrile radical) in the range of 5.1–129.4 were obtained by the manipulation of number-average molar mass data. Values of kpkt of approximately 2 × 10?5 L mol?1 s?1 were found. Trommsdorff types of effect are absent from these systems. 相似文献
5.
R. Velichkova I. M. Panayotov J. Doicheva N. Manolova 《Journal of polymer science. Part A, Polymer chemistry》1983,21(1):17-24
The initiation reaction of the polymerization of α-methylstyrene by trityl tetrachloroferate and tritylhexachloroantimonate in 1,2-dichloroethane at 20°C was studied. The rate constants were 14 × 10?3 and 27 × 10?3 L mol?1s?1, respectively. The dissociation constants of tritylterachloroferate (Kd = 0.88 × 10?4M?1) and tritylhexachloroantimonate (Kd = 2.64 × 10?4M?1) was determined. The effect of electron acceptors and donors on the dissociation equilibrium and initiation rate was investigated. It was shown that in strongly dissociated ion pairs such as stable carbenium salts the electron donors and acceptors have no appreciable effect on the magnitude of the dissociation. The temperature dependence of the rate constants in the ?20–+20°C range yielded the following thermodynamic parameters for trityltetrachloroferate: Ei = 8.54 kcal/mol; A = 3.2 × 104 mol?1s?1; ΔH* = 8 kcal/mol; and S* = ?39.8 eu. 相似文献
6.
Takeshi Wada Terutaka Watanabe Masaaki Takehisa 《Journal of polymer science. Part A, Polymer chemistry》1972,10(10):3039-3052
The radiation-induced heterogeneous polymerization of ethylene in ethyl alcohol was carried out in a reactor with a capacity of 100 ml under the following reaction conditions: temperature, 24 ± 3°C; pressure, 200–400 kg/cm2; amount of ethyl alcohol, 30–70 ml; dose rate, 3.7 × 104?1.05 × 105 rad hr. The effects of amount of ethyl alcohol, pressure, and dose rate on the rate of polymerization at the steady state, the amount of polymerized monomer, the molecular weight of polymer, and the number of polymer chains were studied compared with the results obtained in the polymerization in tert-butyl alcohol. It was found that there is an acceleration period in the early stage of reaction followed by a steady state. The rate of polymerization was maximum when about 50 ml of ethyl alcohol was used. The molecular weight of polymer increased with a decrease in the amount of ethyl alcohol. The dependences of pressure (p) and dose rate (I) on the rate of polymerization at steady state (Rs) and the molecular weight of polymer (M?n) were expressed as follows; Rs ∝ p0.74, M?n ∝ p0.3?0.4, Rs ∝ I0.9 and M?n ∝ I?0.1 ?0.0. The results were analyzed by a kinetic treatment based on a reaction mechanism containing both first-and second-order terminations. The rate constant of first-order termination by radical occlusion was considerably larger than that in the polymerization in tert-butyl alcohol, because the affinity of ethyl alcohol for polyethylene is smaller than that of tert-butyl alcohol. It was found that chain transfer to ethyl alcohol takes place easily and the G value of ethyl alcohol for initiation is larger than 1.5. 相似文献
7.
Dinabandhu Pramanick Jyotish Sarkar Ramanath Bhattacharyya 《Journal of polymer science. Part A, Polymer chemistry》1988,26(5):1457-1463
The reactions of OH radical with Cl?, Br?, I?, and F? ions have been studied by entrapping the product radicals as polymer endgroup which have been detected and estimated by the sensitive dye partition technique. The rate constants of the reactions with Br?, Cl?, and F? ions have been determined to be 1.51 × 109, 1.32 × 109, and 0.92 × 109 L mol?1 s?1, respectively at 25°C and pH 1.00. Oxidation of I? ions liberates I, which inhibits the polymerization and the reaction could not be followed by polymer endgroup analysis. The observed order of reactivity Br? > Cl? > F? is in accordance with the electron affinities of the halide ions. The acidity of the reaction medium has a strong influence on the rate of reaction. With Br? ions, the rate constant of the reaction falls from 1.51 × 109 to 0.75 × 109 L mol?1 s?1 at 25°C as the pH is raised from 1.0 to 2.8. The method is simple and accurate and can be applied to study very reactive radicals. 相似文献
8.
Valrie Sciannamea Maxime Bernard Jean‐Marie Catala Robert Jrme Christophe Detrembleur 《Journal of polymer science. Part A, Polymer chemistry》2006,44(21):6299-6311
The C‐phenyl‐N‐tert‐butylnitrone/azobisisobutyronitrile pair is able to impart control to the radical polymerization of n‐butyl acrylate as long as a two‐step process is implemented, that is, the prereaction of the nitrone and the initiator in toluene at 85 °C for 4 h followed by the addition and polymerization of n‐butyl acrylate at 110 °C. The structure of the in situ formed nitroxide has been established from kinetic and electron spin resonance data. The key parameters (the dissociation rate constant, combination rate constant, and equilibrium constant) that govern the process have been evaluated. The equilibrium constant between the dormant and active species is close to 1.6 × 10?12 mol L?1 at 110 °C. The dissociation rate constant and the activation energy for the C? ON bond homolysis are 1.9 × 10?3 s?1 and 122 ± 15 kJ mol?1, respectively. The rate constant of recombination between the propagating radical and the nitroxide is as high as 1.2 × 109 L mol?1 s?1. Finally, well‐defined poly(n‐butyl acrylate)‐b‐polystyrene block copolymers have been successfully prepared. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6299–6311, 2006 相似文献
9.
N. Ya. Kaloforov E. Borsig 《Journal of polymer science. Part A, Polymer chemistry》1973,11(10):2665-2680
The study of chain-transfer reactions in thermal and AIBN-initiated polymerization of styrene is aimed at the determination of transfer constants to the solvents at 60°C. For thermal polymerization the transfer constants Cs to acetone, chloroform, and chloroform mixed with acetone are 3.2 × 10?5, 4.1 × 10?5, and 4.4 × 10?5, respectively. In the case of AIBN-initiated polymerization, the transfer constant of chloroform in the mixture acetone–chloroform is Cs = 3.3 × 10?4. All these transfer constants are average values. It has been found that neither acetone nor chloroform satisfies the Mayo equation in the presence of transfer agent very well. These anomalies can be explained by assuming a complexation phenomenon. The changes in the polarity and resonance are taken into account. It is considered that in the chain-transfer reactions under investigation, the association or complex-forming ability of solvent and monomer or polymer play a role. In studying the chain-transfer reaction in the acetone–chloroform solvent mixture another phenomenon affecting the determination of the chain transfer constant is assumed. This phenomenon consists in formation of associates in which both solvents participate. 相似文献
10.
Abstract The polymerization of styrene (St) initiated by 1,4-dimethyl-1,4-bis(p-anisyl)-2-tetrazene (1a) was studied kinetically in benzene. The polymerization proceeds through a radical mechanism. The rate of polymerization is proportional to [1a]0.5 and [St]1.0. The overall activation energy for the polymerization is found to be 81.2 kJ/mol within the temperature range of 65 to 80°C. The activation parameters for the decomposition of 1a at 70°C are kd = 1.88 × 10?5s?1, δH? = 133.1 kJ/mol, and δS? = 29.9 J/mol·deg. 相似文献
11.
The charge-transfer complex formed between an amine and carbon tetrachloride can initiate the polymerization of vinyl monomers in a nonaqueous solvent such as dimethylsulfoxide. Here we use cyclopentylamine (CPA) and heptylamine (HA) as the donor compounds for charge-transfer initiation of the polymerization of methl methacrylate (MMA). The rate of polymerization Rp = k[MMA]1 [amine]0.5 [CCl4]0.5 when [CCl4] [amine] ≤ 1; when [CCl4] [amine] < 1, Rp becomes independent of [CCl4] and Rp = k[MMA]1.5 [amine]0.5. The average constant at 60°C for the polymerization of MMA in terms of monomer were (1.66 ± 0.03) × 10?5 and (1.46 ± 0.04) × 10?5 s?1 with CPA and HA, respectively, when [CCl4] [amine] ≤ 1, and (1.16 ± 0.04) × 10?5 and (1.39 ± 0.08) × 10?1 L/mol·s when [CCl4]/[amine] < 1. 相似文献
12.
Karla Delgado‐Rodríguez Francisco J. Enríquez‐Medrano Adriana Berenice Espinoza‐Martínez Gastn P. Barreto Gabriel Merino Graciela Morales 《Journal of polymer science. Part A, Polymer chemistry》2019,57(9):997-1007
The decomposition rate constant (kd) of pinacolone diperoxide (PDP, 3,6‐diterbutyl‐3,6‐dimethyl‐1,2,4,5‐tetraoxacyclohexane) in methyl methacrylate (MMA) is determined by the kinetic study of its thermal decomposition at temperatures from 110 °C to 140 °C. The calculated kd values for PDP are higher than the corresponding values previously determined and reported for diethyl ketone triperoxide (DEKTP, 3,3,6,6,9,9‐hexaethyl‐1,2,4,5,7,8‐hexaoxacyclononane), for example, at 140 °C the kd for PDP is 75.4 × 10?5 s?1, while for DEKTP, it is 50.6 × 10?5 s?1. The difference in the kd between 130 °C and 140 °C indicates that the decomposition mechanism, sequential and/or concerted, is a function of temperature. The conformations of both initiators justify the higher kd for PDP in MMA than DEKTP, where one single conformer is found for PDP, whereas 212 conformers are found for DEKTP. Bulk polymerization of MMA using PDP as the initiator reveals also the presence of an induction period, such as in DEKTP case. This work provides mechanistic insights into the interactions among the bifunctional cyclic peroxide PDP and the MMA monomer and their influence on the polymerization kinetics. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 997–1007 相似文献
13.
The effects of oxygen on the liquid-phase polymerization of vinyl chloride at 55°C in the presence of an added initiator, bis(4-tert-butylcyclohexy1) peroxydicarbonate, (Perkadox 16), have been studied by tumbled dilatometry. A conventional kinetic scheme involving a predominant cross-termination reaction is proposed to explaine the dependence of the induction period on initial oxygen concentration and initiator concentration. The degree of conversion of the initial oxygen to peroxidic compounds did not exceed 30% by weight under any experimental conditions employed, and the existence of other oxidation products such as formaldehyde, carbon monoxide, and methanol has been demonstrated. Radical decomposition reactions may produce some of the oxidation products. At 55°C, the average velocity constant for decomposition of vinyl chloride polyperoxides in dichloromethane solution was 8 × 10?5 sec?1 compared with 6.6 × 10?5 sec?1 for Perkadox 16. Perkadox 16 has been used as an initiator in a dilatometric study of the homogeneous polymerization of styrene at 60°c. Molecular weights of the polymers were determined viscometrically or by the use of gel-permeation chromatography. The results indicate that no transfer to initiator occurs in this systems. 相似文献
14.
The aqueous polymerization of methyl methacrylate initiated by the bromate-thiourea redox system in dilute HC1 has been investigated under nitrogen atmosphere. The rate of polymerization increases with increasing concentration of thiourea in the range 5 × 10?3?10 × 10?3 M. The percentage of conversion increases with increasing concentration of the catalyst, but beyond 1.5 × 10?2 M, there is a decreasing trend in the rate of polymerization. The rate of polymerization increases with increasing monomer concentration, but beyond 0.184 M the polymerization rate decreases due to gel effect. The rate of polymerization increases with temperature up to 35°C and beyond 40°C a decreasing trend is noticed. The effect of water miscible organic solvents, certain neutral salts on the rate of polymerization has also been investigated. 相似文献
15.
Baowei Mao Leong‐Huat Gan Yik‐Yuen Gan Xiaoshi Li Palaniswamy Ravi Kam‐Chiu Tam 《Journal of polymer science. Part A, Polymer chemistry》2004,42(20):5161-5169
Very well‐controlled polymerizations of 2‐(dimethylamino)ethyl methacrylate (DMAEMA) and 2‐(diethylamino)ethyl methacrylate (DEAEMA) in aqueous and methanolic solutions via atom transfer radical polymerization (ATRP) at ambient temperature were demonstrated. Poly(DMAEMA) and poly(DEAEMA) of low polydispersity index (PDI) of ~1.07 were obtained using the p‐toluenesulfonyl chloride/CuCl/1,1,4,7,10,10‐hexamethyl‐triethylenetetramine (p‐TsCl/CuCl/HMTETA) system. Excellent control of polymerization was achieved even in pure methanol. This is in contrast with the very poor control of DMAEMA ATRP in methanol reported previously using a different intiator/catalyst/ligand system. The initiator p‐TsCl underwent hydrolysis reaction in aqueous methanolic solutions with a second‐order rate constant of 6.1 × 10?4 dm3 mol?1 s?1 at 25 °C. Both poly(DMAEMA) and poly(DEAEMA) retained almost full chlorine‐functionization at the chain ends. Well‐defined block copolymers of DEAEMA and DMAEMA were successfully obtained by starting with either macroinitiators of DEAEMA or DMAEMA. Other well‐defined diblock copolymers could be prepared using these macroinitiators. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5161–5169, 2004 相似文献
16.
A. N. Ponomarev Yu. L. Moskvin S. D. Babenko 《Russian Journal of Electrochemistry》2007,43(3):273-278
The transport properties of separating membranes MF-4SK are studied during electrolysis of H2O in solutions of KOH. The effective diffusion coefficients of molecules of KOH and H2O and the transfer coefficients of ions K+ and OH? and molecules of H2O are measured at KOH concentrations reaching 11 M, currents reaching 0.31 A cm?2, at ambient temperature and at 80°C. In contact with a KOH solution in the concentration interval 0.1 to 11 M, the membranes that initially swelled in H2O lose a considerable fraction of water that was present in them and the overall volume of clusters and solution-filled channels in them noticeably decreases. The coefficients of transfer by current of ions K+ out of anodic compartment into cathodic and the OH? ions in the reverse direction, respectively, happen to be equal to about 0.6 and 0.4 at ambient temperature and 0.8 and 0.2 at 80°C. The coefficients of transfer of water molecules out of the anodic volume into the cathodic volume in the process of electrolysis happen to be in the limits 1.6–1.9 at ambient temperature and in the limits 2.2–2.8 at 80°C. The effective diffusion coefficients of molecules of KOH and H2O at moderate concentrations of KOH (5.6 M) amount to ~2.6 × 10?7 and 30 × 10?7 cm2s?1 at ambient temperature and ~4 × 10?7 and 61 × 10?7 cm2s?1 at 80°C, respectively. At a high concentration of KOH (~10 M) these quantities substantially diminish. 相似文献
17.
Abstract Gamma ray induced polymerization of N,N'-methylenebisacrylamide (MBA) in aqueous solution has been studied. Rates of polymerization have been determined as a function of dose, dose rate, and monomer concentration. Polymerization mechanism was found to be free radical with chain propagation step involving ring formation. About 90% conversion was achieved in 25 minutes of irradiation (dose rate 1.54 × 1018 eV dm?3 s?1) of MBA solution (36 mmol). The polymerization rates were found to vary from 1.9 × 10 4 to 5.6 × 10?4 mol dm?3 s?1 when the monomer concentrations were varied between 80–164 mmols. The value of the constant kp/kt 1/2 was calculated to be 9.85 for the dose rate of 1.54 × 1018 eV dm?3 s?1. The precipitated polymer showed mono disperse particles of diameter of about 170 nm. The polymer was found to be highly crosslinked and insoluble in any solvent. 相似文献
18.
Nrusingha C. Pati Subasini Lenka Padma L. Nayak Trijama R. Mohanty 《Journal of polymer science. Part A, Polymer chemistry》1978,16(2):343-351
The aqueous polymerization of acrylonitrile initiated by an acidified bromate–thiourea redox system has been studied under nitrogen atmosphere. The rate of polymerization is independent of thiourea concentration over the range 2–9 × 10?3M and reaches maximum at 9 × 10?3M. The rate varies linearly with [monomer]. The initial rate of polymerization as well as the maximum conversion increases within the range of 4–22.5 × 10?3M KBrO3, but beyond 22.5 × 10?3M the rate of polymerization decreases. The initial rate and the limiting conversion increases with increasing polymerization temperature in the range 30–45°C; and beyond 45°C they decrease. The effect of certain neutral salts, water-soluble solvents, and micelles of cationic, anionic, and nonionic surfactants on the rate of polymerization has been investigated. 相似文献
19.
The theta temperature for the system poly(o-chlorostyrene)-methyl ethyl ketone has been determined as 24·5°. The samples used in the determination were prepared by radical polymerization. The dependence of intrinsic viscosity on molecular weight has been measured in methyl ethyl ketone at 24·5° and found to be . The ratio 〈s=2〉/M was found, by light scattering, to be 5·60 × 10?18 cm2. Analysis of the solution properties indicates that the Kurata-Yamakawa theory is valid in the vicinity of the Flory temperature (UCST). 相似文献
20.
It has been shown by ESR spectroscopy that the title reaction involves abstraction of hydrogen from the phosphite, since at ?10°C the reaction has a kinetic deuterium isotope effect, kH/kD, or ~3. The rate constant for hydrogen abstraction is c. 2 × 104 M?1 s?1. There is no significant addition of alkoxyl radicals to the phosphite. 相似文献