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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 441-453 
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; molecular weight distribution ; mathematical model ; Monte Carlo method ; computer simulation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Monte Carlo simulation model for the kinetics of emulsion polymerization is proposed. In the present model, the formation of each polymer molecule is simulated by the use of only a couple of probability functions; therefore, the calculation can be handled well even on personal computers. It is straightforward to account for virtually any kinetic event, such as the desorption of oligomeric radicals and chain length dependence of kinetic parameters, and as a consequence very detailed information such as the full distributions of the dead polymer molecular weights and the macroradicals among various polymer particles can be obtained. When bimolecular terminations are the dominant chain stoppage mechanism, the instantaneous molecular weight distribution (produced in a very small time interval) becomes broader than that for homogeneous polymerizations due to a higher possibility that short and long polymer radicals react with each other if bimolecular reactions are fast enough. The increase in the polydispersity of the MWD is fairly large, especially when bimolecular termination by disproportionation is significant; however, the gel permeation chromatography (GPC) may not be a suitable analytical technique to detect such broadening since oligomeric peaks may not be observed in the elution curve. The present simulation method provides greater insight into the complicated phenomena of emulsion polymerizations. © 1995 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 901-910 
    ISSN: 0887-6266
    Keywords: nonlinear free radical polymerization ; chain transfer to polymer ; terminal double-bond polymerization ; molecular weight distribution ; branching density distribution ; mathematical model ; Monte Carlo method ; method of moments ; poly (vinyl acetate) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new simulation model for the kinetics of long-chain branching formed via chain transfer to polymer and terminal double-bond polymerization is proposed. This model is based on the branching density distribution of the primary polymer molecules. The theory of branching density distribution is that each primary polymer molecule experiences a different history of branching and provides information on how each primary polymer molecule is connected with other chains that are formed at different conversions, therefore making possible a detailed analysis on the kinetics of the branched structure formation. This model is solved by applying the Monte Carlo method and a computer-generated simulated algorithm is proposed. The present model is applied to a batch polymerization of vinyl acetate, and various interesting structural changes occurring during polymerization (i.e., molecular weight distribution, distribution of branch points, and branching density of the largest polymer molecule) are calculated. The present method gives a direct solution for the Bethe lattice formed under nonequilibrium conditions; therefore, it can be used to examine earlier theories of the branched structure formation. It was found that the method of moments that has been applied successfully to predict various average properties would be considered a good approximation at least for the calculation of not greater than the second-order moment in a batch polymerization. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1191-1202 
    ISSN: 0887-6266
    Keywords: molecular weight distribution ; network formation ; crosslinking density ; gel ; radius of gyration ; crosslinked structure ; Monte Carlo method ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular weight distribution (MWD) of crosslinked polymer molecules formed during polymeric network formation is the sum of the fractional MWDs containing 0, 1, 2, 3, … crosslinkages. The MWD for polymer molecules containing k crosslinkages is investigated for the random crosslinking of polymer chains whose initial MWD is given by the Schulz-Zimm distribution. For a very narrow initial MWD, each fractional MWD with k = 0, 1, 2, … is independent and a multimodal distribution is obtained for the whole distribution. When the initial MWD is uniform, the average crosslinking density within the polymer fraction whose degree of polymerization is r, ρr is simply given by ρr = ρgel,c - 2/r irrespective of the extent of crosslinking reaction where ρgel,c is the crosslinking density within gel fraction at the gel point. On the other hand, the MWDs with k crosslinkages overlap each other with different k values significantly for the broader initial distributions, and ρr increases with the progress of crosslinking reactions. The value of ρr increases with increasing r but levels off asymptotically at large r. The average crosslinking density of polymer molecules containing k crosslinkages ρk is an increasing function of k but soon reaches a plateau; sooner for the broader initial MWDs. For k ≥ 1, ρk is always larger than the average crosslinking density of the whole reaction system ρ in the pregelation period, i.e., in terms of the crosslinking density, the difference between polymer molecules with and without crosslinkage is most significant. In general, the average crosslinking density ρ, which is convenient to use in describing the nature of the whole reaction system, cannot be considered as a characteristic degree of crosslinking for polymer molecules containing at least one crosslinkage. Consideration of the bivariate distribution of r and k reveals important aspects of the polymeric network formation that have been obscured in the conventional theories in which the averages including linear polymers are solely considered. © 1995 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1403-1413 
    ISSN: 0887-6266
    Keywords: microgels ; emulsion polymers ; molecular weight distribution ; crosslinking ; Monte Carlo method ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Microgel formation during emulsion copolymerization of methyl methacrylate and ethylene glycol dimethacrylate is investigated both experimentally and theoretically. It was found that the average crosslinking density is fairly high even from a very early stage of polymerization. The molecular weight distribution (MWD) development in emulsion crosslinking copolymerization is completely different from that in homogeneous polymerization. Because the maximum molecular weights allowed to exist is limited by the particle size, a comprehensive model for the MWD development in nonlinear emulsion polymerization must account for the size of polymerization locus properly. During the formation of microgels, a drastic change in the weight-average molecular weights, which is characteristic of gelation in homogeneous media, is not always required. In a typical microgel formation process where a large mole fraction of divinyl monomer is used, the average molecular weights may increase just linearly with conversion in which a sharp MWD shifts to higher molecular weights with the progress of polymerization. It is shown that the microgels formed in emulsion polymerization are characterized as intramolecularly crosslinked macromolecules that occupy a very large weight fraction in each polymer particle. © 1996 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2099-2104 
    ISSN: 0887-6266
    Keywords: molecular weight distribution ; polyradical ; gel ; polymer modification ; nonlinear polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: No abstract.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2423-2433 
    ISSN: 0887-6266
    Keywords: gelation theory ; nonlinear polymerization ; nonrandom crosslinking ; molecular weight distribution ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: On the basis of the first-order Markovian statistics, we propose a general matrix formula for the weight-average molecular weight of crosslinked polymer systems, explicitly given by M̄w = M̄w,0 + WX0 (I - X)-1 Sf. This equation is valid for both step and chain-growth polymerizations, including those in a nonequilibrium state irrespective of the reactor types used. In the context of the present theory, the onset of gelation is simply stated as a point at which the largest eigenvalue of the matrix X reaches unity (i.e., det(I - X) = 0). The present theory provides a unified point of view for various types of gelling systems. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2423-2433, 1998
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 357-371 
    ISSN: 0887-6266
    Keywords: gelation theory ; nonlinear polymerization ; molecular weight distribution ; branched polymers ; polymer modification ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A Markovian model is proposed for nonrandom branching reactions, by using free-radical polymerization that involves chain transfer to polymer as an example. Free-radical polymerizations are kinetically controlled; therefore, each primary polymer molecule experiences different history of branched structure formation. By assuming that the primary chains with the identical birth time conform to the same chain connection probabilities, the nonlinear structural development can be viewed as a system in which the primary chains formed at different birth times are combined into nonlinear polymers in accordance with the first-order Markov chain statistics. An explicit formula for the weight-average chain length is derived in a matrix form. The onset of gelation is simply stated as a point at which the largest eigenvalue of the transition matrix X reaches unity, i.e., det(X - I) = 0. This criterion for the onset of gelation can be considered as an extension of the Flory/Stockmayer theory to a nonequilibrium reaction system. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 357-371, 1998
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1363-1371 
    ISSN: 0887-6266
    Keywords: molecular weight distribution ; nonlinear free-radical polymerization ; branching density distribution ; chain transfer to polymer ; long-chain branches ; gelation ; Monte Carlo method ; method of moments ; mathematical model ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new theory to predict the molecular weight distribution in free radical polymerization that includes chain transfer to polymer is proposed. This theory is based on the branching density distribution of the primary polymer molecules. The branching density distribution provides the information on how each chain is connected to other chains, and therefore, a full molecular weight distribution can be calculated by application of the Monte Carlo simulation. The present theory accounts for the history of the generated branched structure and can be applied to various reaction systems that involve branching and crosslinking regardless of the reactor types used. The present simulation confirmed the validity of the method of moments in a batch polymerization proposed earlier. It was shown clearly why gelation never occurs by chain transfer to polymer without the assistance of other interlinking reaction such as bimolecular termination by combination. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 841-853 
    ISSN: 0887-6266
    Keywords: molecular weight distribution ; branching density distribution ; radius of gyration ; Monte Carlo method ; branched polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Monte Carlo sampling technique is used to investigate the branched structure formation during free-radical polymerization that involves chain transfer to polymer. This method accounts for the history of the generated branched structure and can provide virtually any structural information, because one can observe each polymer molecule directly. In this paper, we investigate the whole molecular weight distribution (MWD) for both pre- and postgelation periods, the MWDs for polymer molecules containing 0, 1, 2, 3, … branch points, the branching density of polymer molecules as functions of both size and the number of branch points, the spatial distribution of the branched chains at the theta state, etc. Contrary to the term ‘long-chain’ branching, many branch chains are relatively small, and the branched structures formed are significantly different from those usually depicted to introduce ‘branched polymers’ in many introductory textbooks. The radii of gyration at the theta state can be approximated by the Zimm-Stockmayer equation for random branching, in spite of various violations against the assumptions used in deriving the equation © 1995 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1415-1422 
    ISSN: 0887-6266
    Keywords: microgels ; gelation ; emulsion polymers ; seeded polymerization ; molecular weight distribution ; crosslinking ; Monte Carlo method ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Microgel formation in seeded emulsion copolymerization of methyl methacrylate and ethylene glycol dimethacrylate is investigated both experimentally and theoretically. By introducing seed latex, the network structure development can be changed significantly. Even when the crosslinking density development takes a similar pattern as the crosslinking copolymerization in homogeneous media, the molecular weight development shows both types of behavior that is characteristic of emulsion polymerization without seed latex and of homogeneous polymerization, depending on the primary polymer chain length and the mole fraction of the divinyl monomer used. Once the microgels are formed, the weight-average molecular weight increases just linearly with conversion due to a very small locus of polymerization. The present investigation reveals important characteristics of gelation phenomena in a limited space. © 1996 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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