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1.
Jos Luis De La Fuente Enrique Lpez Madruga 《Journal of polymer science. Part A, Polymer chemistry》2000,38(1):170-178
Chain‐transfer constants were evaluated for n‐dodecanethiol in the homopolymerization of styrene (S) and methyl methacrylate (MMA). The polymerizations were carried out in benzene at 50 °C with different amounts of 2,2′‐azobisisobutyronitrile as the initiator. The new chain length distribution (CLD) analytical method was used and compared to the traditional Mayo method. The chain‐transfer‐constant values were independent of the initiator concentration and slightly higher (by a factor of 1.1 for MMA and 1.2 for S) when obtained according to the CLD method compared to the Mayo method. The chain‐transfer constant for S was 20 times higher than for MMA. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 170–178, 2000 相似文献
2.
C. Sayer E. L. Lima J. C. Pinto G. Arzamendi J. M. Asua 《Journal of polymer science. Part A, Polymer chemistry》2000,38(2):367-375
The effect of a chain‐transfer agent (CTA) on the kinetics and molecular weight distribution of the methyl methacrylate/butyl acrylate semicontinuous emulsion polymerization was investigated. The dodecanethiol had a slight effect on the reaction rate but significantly affected the secondary nucleation. The effect of the CTA concentration on the gel formation and the effect of the reaction conditions on the mass‐transfer limitations of the CTA are discussed. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 367–375, 2000 相似文献
3.
Emulsion terpolymerization of butyl acrylate/methyl methacrylate/vinyl acetate: Experimental results
Marc A. Dub Alexander Penlidis 《Journal of polymer science. Part A, Polymer chemistry》1997,35(9):1659-1672
A systematic study of the terpolymerization of butyl acrylate/methyl methacrylate/vinyl acetate (BA/MMA/VAc) was conducted. In this stage of the study, batch emulsion terpolymerizations were performed in a 5 L stainless steel pilot plant reactor. The experiments were designed using a Bayesian (optimal) technique. The polymers produced were characterized for conversion, composition, molecular weight, and particle size. Conversion, terpolymer composition, number- and weight-average molecular weight, and average particle size results are discussed in light of the influence of seven factors and the interaction of these factors. The factors studied include monomer feed composition, initiator concentration, chain transfer agent concentration, impurity concentration, initiator type, emulsifier concentration, and temperature. A “two-stage rate” phenomenon, similar to that occurring in bulk co- and terpolymerization and emulsion copolymerization of acrylic/vinyl acetate systems was observed in the conversion, composition and molecular weight data. Furthermore, an interesting yet often ignored effect of impurities on emulsion polymerization kinetics was explained. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35 : 1659–1672, 1997 相似文献
4.
Michael J. Devon Alfred Rudin 《Journal of polymer science. Part A, Polymer chemistry》1986,24(9):2191-2198
Free radical chain transfer constants have been measured by copolymerizing styrene and butyl acrylate in emulsion at 60°C. Some improvements to this experimental technique are reported and estimates are given of the sensitivity of the calculated values to experimental uncertainties. Monomer chain transfer constants were found to be 1.2 × 10?4 (styrene) and 2.5 × 10?4 (butyl acrylate). The sum of the cross-transfer constants is 2.7 × 10?4. The activation energy for chain transfer to styrene monomer is found to be 24 Kcal/mol in the 44°–60°C range. 相似文献
5.
Rodrigo París Jos Luis de la Fuente 《Journal of polymer science. Part A, Polymer chemistry》2006,44(18):5304-5315
Functional spontaneous gradient copolymers of allyl methacrylate (A) and butyl acrylate (B) were synthesized via atom transfer radical polymerization. The copolymerization reactions were carried out in toluene solutions at 100 °C with methyl 2‐bromopropionate as the initiator and copper bromide with N,N,N′,N″,N″‐pentamethyldiethylenetriamine as the catalyst system. Different aspects of the statistical reaction copolymerizations, such as the kinetic behavior, crosslinking density, and gel fraction, were studied. The gel data were compared with Flory's gelation theory, and the sol fractions of the synthesized copolymers were characterized by size exclusion chromatography and nuclear magnetic resonance spectroscopy. The copolymer composition, demonstrating the gradient character of the copolymers, and the microstructure were analyzed. The experimental data agreed well with data calculated with the Mayo–Lewis terminal model and Bernoullian statistics, with monomer reactivity ratios of 2.58 ± 0.37 and 0.51 ± 0.05 for A and B, respectively, an isotacticity parameter for A of 0.24, and a coisotacticity parameter of 0.33. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5304–5315, 2006 相似文献
6.
Jos M. Senz Jos M. Asua 《Journal of polymer science. Part A, Polymer chemistry》1996,34(10):1977-1992
Monodisperse copolymer particles from 1.1 to 2.6 μm in diameter were obtained by unseeded batch dispersion copolymerization of styrene and butyl acrylate in an ethanol–water medium. A two-level factorial design using bottle polymerizations was initially carried out including the following variables: stabilizer concentration, initiator concentration, polarity of the dispersion medium, initial monomer concentration, and temperature. Once the region of experimental conditions in which monodisperse latexes can be prepared was identified, further effort was devoted to analyze the effect of other variables. It was found that the temperature at which nucleation occurs and the evolution of the temperature after the onset of nucleation were critical to obtain monodisperse particles. The particle size increased with increasing initial monomer concentration and ethanol–water weight ratio, and decreasing stabilizer concentration. A minimum quantity of emulsifier was necessary to avoid coalescence of particles and to obtain monodisperse particles. © 1996 John Wiley & Sons, Inc. 相似文献
7.
8.
Mircea Teodorescu 《European Polymer Journal》2002,38(5):841-846
The free-radical copolymerization of methyl methacrylate (MMA) with styrene (St) in the presence of 2-mercaptoethanol (ME) was investigated in order to obtain ω-hydroxy oligomers with random copolymer-type chains of various compositions and molecular weights. Polymerizations at three different MMA/St molar ratios were carried out, while keeping constant the ME/monomer ratio. Monomer mixtures richer in MMA than in St were employed in order to attempt preparing lower polydispersity oligomers with monomodal molecular weight distribution (MWD). The molecular weights of the resulting oligomers increased with both conversion and MMA fraction in the feed, while polydispersities increased with conversion and decreased with MMA concentration in the initial monomer mixture. For the lower MMA fractions in the monomer feed, bimodal MWDs resulted beyond a certain conversion due to the faster relative consumption of ME than of monomer. Based on the pseudo-kinetic rate constant method, apparent chain transfer constants corresponding to the three different compositions of the monomer feed were estimated. The values obtained were in good agreement with the evolution of molecular weights and polydispersities with conversion and MMA fraction in the monomer feed. The co-oligomers prepared displayed functionalities around unity, making them suitable for the synthesis of macromonomers. 相似文献
9.
Copolymers of styrene and methyl methacrylate were synthesized by atom transfer radical polymerization using methyl 2‐bromopropionate as initiator and CuBr/N,N,N′,N′,N″‐pentamethyldiethylenetriamine as catalyst. Molecular weight distributions were determined by gel permeation chromatography. The composition of the copolymer was determined by 1H NMR. The comonomer reactivity ratios, determined by both Kelen–Tudos and nonlinear error‐in‐variables methods, were rS = 0.64 ± 0.08, rM = 0.63 ± 0.08 and rS = 0.66, rM = 0.65, respectively. The α‐methyl and carbonyl carbon resonances were found to be compositionally and configurationally sensitive. Complete spectral assignments of the 1H and 13C NMR spectra of the copolymers were done by distortionless enhancement by polarization transfer and two‐dimensional NMR techniques such as heteronuclear single quantum coherence and heteronuclear multiple quantum coherence. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2076–2085, 2006 相似文献
10.
Manuel Gaboyard Thomas Jeanmaire Christian Pichot Yves Hervaud Bernard Boutevin 《Journal of polymer science. Part A, Polymer chemistry》2003,41(16):2469-2480
A series of methyl methacrylate, butyl acrylate, and phosphonated methacrylate (MAPHOS) copolymers were prepared by seeded semicontinuous emulsion polymerization under monomer‐starved conditions by varying the amount and nature of phosphonated methacrylates (diester, monoacid, and diacid). The effects on the kinetics, molecular weight distribution, and particle size distribution were investigated. The molecular weights and particle growth were affected by the amount of acidic MAPHOS in the recipe. Secondary nucleation occurred above a critical concentration of acidic MAPHOS (5 wt %). Characterization of the latices by elemental analysis provided information on the phosphonic acid location and showed that phosphonic oligomers were formed in the aqueous phase. Particle size data and electrophoretic behavior of the latex afforded a discussion on the particle surface morphology. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2469–2480, 2003 相似文献
11.
Synthesis of Poly(n‐butyl acrylate/methyl methacrylate)/CNC Latex Nanocomposites via In Situ Emulsion Polymerization
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Cellulose nanocrystals (CNCs) are renewable, nontoxic and naturally available organic nanoparticles derived from cellulosic resources such as cotton and wood pulp. Poly(n‐butyl acrylate‐co‐methyl methacrylate)/CNC latexes are successfully synthesized via in situ emulsion polymerization. The effect of CNC loading on overall conversion, polymer particle size, glass transition temperature (Tg), gel content, latex viscosity, and storage and loss moduli of dried latex are studied. While the effect of CNC content on overall conversion, polymer particle size, and Tg of the resulting latexes is negligible, significant increase in gel content, latex viscosity, and storage and loss moduli are observed.
12.
Qinggao Ma Karen L. Wooley 《Journal of polymer science. Part A, Polymer chemistry》2000,38(Z1):4805-4820
Atom transfer radical polymerization conditions with copper(I) bromide/pentamethyldiethylenetriamine (CuBr/PMDETA) as the catalyst system were employed for the polymerization of tert‐butyl acrylate, methyl acrylate, and styrene to generate well‐defined homopolymers, diblock copolymers, and triblock copolymers. Temperature studies indicated that the polymerizations occurred smoothly in bulk at 50 °C. The kinetics of tert‐butyl acrylate polymerization under these conditions are reported. Well‐defined poly(tert‐butyl acrylate) (PtBA; polydispersity index = 1.14) and poly(methyl acrylate) (PMA; polydispersity index = 1.03) homopolymers were synthesized and then used as macroinitiators for the preparation of PtBA‐b‐PMA and PMA‐b‐PtBA diblock copolymers in bulk at 50 °C or in toluene at 60 or 90 °C. In toluene, the amount of CuBr/PMDETA relative to the macroinitiator was important; at least 1 equiv of CuBr/PMDETA was required for complete initiation. Typical block lengths were composed of 100–150 repeat units per segment. A triblock copolymer, composed of PtBA‐b‐PMA‐b‐PS (PS = polystyrene), was also synthesized with a well‐defined composition and a narrow molecular weight dispersity. The tert‐butyl esters of PtBA‐b‐PMA and PtBA‐b‐PMA‐b‐PS were selectively cleaved to form the amphiphilic block copolymers PAA‐b‐PMA [PAA = poly(acrylic acid)] and PAA‐b‐PMA‐b‐PS, respectively, via reaction with anhydrous trifluoroacetic acid in dichloromethane at room temperature for 3 h. Characterization data are reported from analyses by gel permeation chromatography; infrared, 1H NMR, and 13C NMR spectroscopies; differential scanning calorimetry; and matrix‐assisted, laser desorption/ionization time‐of‐flight mass spectrometry. The assembly of the amphiphilic triblock copolymer PAA90‐b‐PMA80‐b‐PS98 within an aqueous solution, followed by conversion into stable complex nanostructures via crosslinking reactions between the hydrophilic PAA chains comprising the peripheral layers, produced mixtures of spherical and cylindrical topologies. The visualization and size determination of the resulting nanostructures were performed by atomic force microscopy, which revealed very interesting segregation phenomena. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 4805–4820, 2000 相似文献
13.
In the reversible addition–fragmentation transfer (RAFT) copolymerization of two monomers, even with the simple terminal model, there are two kinds of macroradical and two kinds of polymeric RAFT agent with different R groups. Because the structure of the R group could exert a significant influence on the RAFT process, RAFT copolymerization may behave differently from RAFT homopolymerization. The RAFT copolymerization of methyl methacrylate (MMA) and styrene (St) in miniemulsion was investigated. The performance of the RAFT copolymerization of MMA/St in miniemulsion was found to be dependent on the feed monomer compositions. When St is dominant in the feed monomer composition, RAFT copolymerization is well controlled in the whole range of monomer conversion. However, when MMA is dominant, RAFT copolymerization may be, in some cases, out of control in the late stage of copolymerization, and characterized by a fast increase in the polydispersity index (PDI). The RAFT process was found to have little influence on composition evolution during copolymerization. The synthesis of the well‐defined gradient copolymers and poly[St‐b‐(St‐co‐MMA)] block copolymer by RAFT miniemulsion copolymerization was also demonstrated. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 6248–6258, 2004 相似文献
14.
Jing Gao Yingwu Luo Rui Wang Bogeng Li Shiping Zhu 《Journal of polymer science. Part A, Polymer chemistry》2007,45(14):3098-3111
The RAFT (co)polymerization kinetics of methyl methacrylate (MMA) and n‐butyl acrylate (BA) mediated by 2‐cyanoprop‐2‐yl dithiobenzoate was studied with various RAFT concentrations and monomer compositions. The homopolymerization of MMA gave the highest rate. Increasing the BA fraction fBA dramatically decreased the copolymerization rate. The rate reached the lowest point at fMMA ~ 0.2. This observation is in sharp contrast to the conventional RAFT‐free copolymerization, where BA homopolymerization gave the highest rate and the copolymerization rate decreased monotonously with increasing fMMA. This peculiar phenomenon can be explained by the RAFT retardation effect. The RAFT copolymerization rate can be described by 〈Rp〉/〈Rp〉0 = (1 + 2(〈kc〉/〈kt〉)〈K〉)[RAFT]0)?0.5, where 〈Rp〉0 is the RAFT‐free copolymerization rate and 〈K〉 is the apparent addition–fragmentation equilibrium coefficient. A theoretical expression of 〈K〉 based on a terminal model of addition and fragmentation reactions was derived and successfully applied to predict the RAFT copolymerization kinetics with the rate parameters obtained from the homopolymerization systems. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3098–3111, 2007 相似文献
15.
K. Ouzineb M. Fortuny Heredia C. Graillat T. F. Mckenna 《Journal of polymer science. Part A, Polymer chemistry》2001,39(16):2832-2846
We carried out emulsion homopolymerizations and copolymerizations of butyl acrylate (BuA) and methyl methacrylate (MMA) with different types and concentrations of surfactants to determine the influence of these parameters on the particle size and particle size distribution and to elucidate the mechanism of particle formation. As expected, the mechanisms of nucleation above and below the critical micelle concentration were very different; however, it was also found that the presence of partially soluble monomers such as MMA in the water phase had a significant influence on the critical micelle concentration of Triton X‐405 (>50%). In addition, the nucleation mechanism during copolymerization seemed to be dominated by BuA, with the number of particles per liter being very similar to the number nucleated during its homopolymerization. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2832–2846, 2001 相似文献
16.
Carmen Fernndez‐Monreal Gerardo Martínez Manuel Snchez‐Chaves Enrique Lpez Madruga 《Journal of polymer science. Part A, Polymer chemistry》2001,39(12):2043-2048
The free‐radical copolymerization of 2‐hydroxyethyl methacrylate with t‐butyl acrylate was carried out at 50 °C in bulk and in 3 mol · L?1 1,4‐dioxane and N,N′‐dimethylformamide solutions. Differences between the apparent reactivity ratios determined in this work indicated a noticeable solvent effect. This is explained with a qualitative bootstrap effect. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2043–2048, 2001 相似文献
17.
Christopher Kowollik Thomas P. Davis 《Journal of polymer science. Part A, Polymer chemistry》2000,38(18):3303-3312
The evolution of molecular weight distributions (MWDs) with monomer conversion in the catalytic chain transfer (CCT) polymerization of methyl methacrylate at 60 °C is investigated by simulation (via the program package PREDICI®) and experiment. A Co(III)‐based complex is used as the precursor for the CCT agent, which is formed in situ by initiator‐derived (2,2′‐azobisisobutyronitrile) radicals to yield the catalytically active Co(II) species. The small shifts seen in the MWD toward lower molecular weights with increasing monomer conversion are shown to be of the same order of magnitude as the associated changes in the MWD in non‐CCT controlled free‐radical polymerization, indicating that no significant change in the MWD with monomer conversion is associated with the CCT process. These results are compared to the evolution of MWDs in conventional chain transfer polymerizations with thiols as transfer agents. A clear shift toward higher molecular weights is seen with increasing monomer conversion, indicating disparate rates of thiol and monomer consumption. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 3303–3312, 2000 相似文献
18.
Krzysztof Matyjaszewski Jian Qiu Nicolay V. Tsarevsky Bernadette Charleux 《Journal of polymer science. Part A, Polymer chemistry》2000,38(Z1):4724-4734
Ultrasonication was applied in combination with a hydrophobe for the copper‐mediated atom transfer radical polymerization of n‐butyl methacrylate in an aqueous dispersed system. A controlled polymerization was successfully achieved, as demonstrated by a linear correlation between the molecular weights and the monomer conversion. The polydispersities of the polymers were small (weight‐average molecular weight/number‐average molecular weight < 1.5). The influence of several factors, including ultrasonication, the amount of the surfactant, and the nature of the initiator, on the polymerization kinetics, molecular weight, and particle size was studied. The polymerization rate and molecular weights were independent of the number of particles and only depended on the atom transfer equilibrium. The final particle size, however, was a function of all the parameters. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 4724–4734, 2000 相似文献
19.
Rodrigo París José Luis De la Fuente 《Journal of Polymer Science.Polymer Physics》2007,45(14):1845-1855
Glass transition temperatures (Tgs) of P(AMA‐co‐BA) copolymers and the corresponding homopolymers, where AMA is allyl methacrylate and BA is n‐butyl acrylate, obtained by means of atom transfer radical polymerization were measured using differential scanning calorimetry. Because of the (pseudoliving) nature of this polymerization technique an increase in molecular weight (MW) is produced as the reaction progresses, which gives rise to an increase in Tgs. This increment can be adequately described by the Fox–Flory's equation in both homopolymers. However, in the spontaneous gradient copolymers of P(AMA‐co‐BA), the expected increase in Tg with the augment of the monomer conversion is compensated by the enrichment of BA as the polymerization reaction progresses. These opposite effects with respect to the Tg values almost balance each other, and therefore no significant influence on the MW or on conversion is found. This fact establishes that Tgs can be used to describe the profile of these gradient copolymers, and can be theoretically determined because of its dependence on the molar fraction in the copolymer. From this dependence on chemical composition along with the experimental behavior, a prediction of the Tg variation with the MW was performed. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 1845–1855, 2007 相似文献
20.
Hormoz Eslami Shiping Zhu 《Journal of polymer science. Part A, Polymer chemistry》2006,44(6):1914-1925
The emulsion atom transfer radical block copolymerization of 2‐ethylhexyl methacrylate (EHMA) and methyl methacrylate (MMA) was carried out with the bifunctional initiator 1,4‐butylene glycol di(2‐bromoisobutyrate). The system was mediated by copper bromide/4,4′‐dinonyl‐2,2′‐bipyridyl and stabilized by polyoxyethylene sorbitan monooleate. The effects of the initiator concentration and temperature profile on the polymerization kinetics and latex stability were systematically examined. Both EHMA homopolymerization and successive copolymerization with MMA proceeded in a living manner and gave good control over the polymer molecular weights. The polymer molecular weights increased linearly with the monomer conversion with polydispersities lower than 1.2. A low‐temperature prepolymerization step was found to be helpful in stabilizing the latex systems, whereas further polymerization at an elevated temperature ensured high conversion rates. The EHMA polymers were effective as macroinitiators for initiating the block polymerization of MMA. Triblock poly(methyl methacrylate–2‐ethylhexyl methacrylate–methyl methacrylate) samples with various block lengths were synthesized. The MMA and EHMA reactivity ratios determined by a nonlinear least‐square method were ~0.903 and ~0.930, respectively, at 70 °C. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1914–1925, 2006 相似文献