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1
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1842817337
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Theory of the interface between immiscible polymers
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Helfand E, Tagami Y. Theory of the interface between immiscible polymers. J Chem Phys. 56:1971;3592-3601.
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(1971)
J Chem Phys
, vol.56
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Helfand, E.1
Tagami, Y.2
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2
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0344935133
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Interfaces between incompatible polymers
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Stamm M, Schubert DW. Interfaces between incompatible polymers. Annu Rev Mater Sci. 25:1995;325-356.
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(1995)
Annu Rev Mater Sci
, vol.25
, pp. 325-356
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Stamm, M.1
Schubert, D.W.2
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3
-
-
0031079027
-
Investigation of the melt interface between polyethylene and polystyrene using neutron reflectivity
-
of outstanding interest. The interfacial width between two of the most important commodity polymers was measured by neutron reflectivity. The resulting small value explains the extreme incompatibility of these two materials.
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Hermes HE, Higgins JS, Bucknall DG. Investigation of the melt interface between polyethylene and polystyrene using neutron reflectivity. of outstanding interest Polymer. 38:1997;985-989 The interfacial width between two of the most important commodity polymers was measured by neutron reflectivity. The resulting small value explains the extreme incompatibility of these two materials.
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(1997)
Polymer
, vol.38
, pp. 985-989
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-
Hermes, H.E.1
Higgins, J.S.2
Bucknall, D.G.3
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4
-
-
0012212358
-
Evidence for capillary waves at immiscible polymer/polymer interfaces
-
of outstanding interest. The interfacial width between two immiscible polymers, one present as a thin film, was measured by neutron reflectivity, and showed a logarithmic dependence on film thickness. This provides strong evidence that the origin of the discrepancy between experimental and theoretical values for the interfacial width is in thermally excited capillary waves.
-
Sferrazza M, Xiao C, Jones RAL, Penfold J, Webster J. Evidence for capillary waves at immiscible polymer/polymer interfaces. of outstanding interest Phys Rev Lett. 78:1997;3693-3696 The interfacial width between two immiscible polymers, one present as a thin film, was measured by neutron reflectivity, and showed a logarithmic dependence on film thickness. This provides strong evidence that the origin of the discrepancy between experimental and theoretical values for the interfacial width is in thermally excited capillary waves.
-
(1997)
Phys Rev Lett
, vol.78
, pp. 3693-3696
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-
Sferrazza, M.1
Xiao, C.2
Jones, R.A.L.3
Penfold, J.4
Webster, J.5
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5
-
-
0000297024
-
Evidence for size effects on interfacial widths in confined thin films
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of outstanding interest. The interfacial width between weakly immiscible polymers is measured, and shown to vary with the square root of the film thickness, indicating an effective short range force acting on the interface.
-
Kerle T, Klein J, Binder K. Evidence for size effects on interfacial widths in confined thin films. of outstanding interest Phys Rev Lett. 77:1996;1318-1321 The interfacial width between weakly immiscible polymers is measured, and shown to vary with the square root of the film thickness, indicating an effective short range force acting on the interface.
-
(1996)
Phys Rev Lett
, vol.77
, pp. 1318-1321
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-
Kerle, T.1
Klein, J.2
Binder, K.3
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6
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0031486532
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Interfaces between coexisting phases of polymer mixtures: Comparison between Monte Carlo simulations and theoretical predictions
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Binder K, Müller M. Interfaces between coexisting phases of polymer mixtures: comparison between Monte Carlo simulations and theoretical predictions. Macromolecular Symposia. 113:1997;207-220.
-
(1997)
Macromolecular Symposia
, vol.113
, pp. 207-220
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-
Binder, K.1
Müller, M.2
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7
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0030082297
-
Interfacial behaviour of compressible polymer blends. Monte Carlo simulation and the lattice fluid theory
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Ypma GJA, Cifra P, Nies E, Bergen ARDV. Interfacial behaviour of compressible polymer blends. Monte Carlo simulation and the lattice fluid theory. Macromolecules. 29:1996;1252-1259.
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(1996)
Macromolecules
, vol.29
, pp. 1252-1259
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-
Ypma, G.J.A.1
Cifra, P.2
Nies, E.3
Bergen, A.R.D.V.4
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8
-
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0030576813
-
Interfacial tension in binary polymer mixtures
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Ermoshkin AV, Semenov AN. Interfacial tension in binary polymer mixtures. Macromolecules. 29:1996;6294-6300.
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(1996)
Macromolecules
, vol.29
, pp. 6294-6300
-
-
Ermoshkin, A.V.1
Semenov, A.N.2
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9
-
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0030594945
-
Influence of chain length of the interface width of an incompatible blend
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Schubert DW, Stamm M. Influence of chain length of the interface width of an incompatible blend. Eur Lett. 35:1996;419-424.
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(1996)
Eur Lett
, vol.35
, pp. 419-424
-
-
Schubert, D.W.1
Stamm, M.2
-
10
-
-
0030171496
-
Interphase and compatibilisation of polymer blends
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Ajji A, Utracki LA. Interphase and compatibilisation of polymer blends. Polym Eng Sci. 36:1996;1574-1585.
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(1996)
Polym Eng Sci
, vol.36
, pp. 1574-1585
-
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Ajji, A.1
Utracki, L.A.2
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11
-
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0030244087
-
Effects of the molecular structure of styrene-isoprene block copolymers on the interfacial characteristics of polystyrene/polyisoprene blends
-
Jo WH, Nam KH, Cho JC. Effects of the molecular structure of styrene-isoprene block copolymers on the interfacial characteristics of polystyrene/polyisoprene blends. J Polym Sci B. 34:1996;2169-2175.
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(1996)
J Polym Sci B
, vol.34
, pp. 2169-2175
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-
Jo, W.H.1
Nam, K.H.2
Cho, J.C.3
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12
-
-
11644285731
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Designing compatibilisers to reduce interfacial tension in polymer blends
-
of outstanding interest. Self-consistent field theory is used to evaluate the relative efficiencies of different copolymer architectures in reducing interfacial tension, illustrating how a first-principles approach to designing optimal compatibilisers might work.
-
Lyatskaya Y, Gersappe D, Gross NA, Balazs AC. Designing compatibilisers to reduce interfacial tension in polymer blends. of outstanding interest J Phys Chem. 100:1996;1449-1458 Self-consistent field theory is used to evaluate the relative efficiencies of different copolymer architectures in reducing interfacial tension, illustrating how a first-principles approach to designing optimal compatibilisers might work.
-
(1996)
J Phys Chem
, vol.100
, pp. 1449-1458
-
-
Lyatskaya, Y.1
Gersappe, D.2
Gross, N.A.3
Balazs, A.C.4
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13
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0030146904
-
Effect of copolymer architecture on the interfacial structure and miscibility of a ternary polymer blend containing a copolymer and two homopolymers
-
Dadmun M. Effect of copolymer architecture on the interfacial structure and miscibility of a ternary polymer blend containing a copolymer and two homopolymers. Macromolecules. 29:1996;3868-3874.
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(1996)
Macromolecules
, vol.29
, pp. 3868-3874
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-
Dadmun, M.1
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14
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0030148453
-
A Monte Carlo simulation of asymmetric random copolymers at an immiscible interface
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Smith GD, Russell TP, Kulasekere R, Ankner JF, Kaiser H. A Monte Carlo simulation of asymmetric random copolymers at an immiscible interface. Macromolecules. 29:1996;4120-4124.
-
(1996)
Macromolecules
, vol.29
, pp. 4120-4124
-
-
Smith, G.D.1
Russell, T.P.2
Kulasekere, R.3
Ankner, J.F.4
Kaiser, H.5
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15
-
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0030575962
-
Mean-field theory of the interface between a homopolymer and a binary polymer mixture
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Genzer J, Faldi A, Composto RJ. Mean-field theory of the interface between a homopolymer and a binary polymer mixture. J Chem Phys. 105:1996;10134-10144.
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(1996)
J Chem Phys
, vol.105
, pp. 10134-10144
-
-
Genzer, J.1
Faldi, A.2
Composto, R.J.3
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16
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0030519618
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On phase equilibria, interfacial tension and phase growth in ternary polymer blends
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He DQ, Kwak S, Nauman EB. On phase equilibria, interfacial tension and phase growth in ternary polymer blends. Macromol Theory Simul. 5:1996;801-827.
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(1996)
Macromol Theory Simul
, vol.5
, pp. 801-827
-
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He, D.Q.1
Kwak, S.2
Nauman, E.B.3
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17
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0030566419
-
Diblock copolymers at a homopolymer-homopolymer interface - A Monte-Carlo simulation
-
Werner A, Schmid F, Binder K, Muller M. Diblock copolymers at a homopolymer-homopolymer interface - a Monte-Carlo simulation. Macromolecules. 29:1996;8241-8248.
-
(1996)
Macromolecules
, vol.29
, pp. 8241-8248
-
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Werner, A.1
Schmid, F.2
Binder, K.3
Muller, M.4
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18
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11644312542
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Bulk and interfacial thermodynamics of a symmetric, ternary homopolymer-copolymer mixture: A Monte Carlo study
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Müller M, Schick M. Bulk and interfacial thermodynamics of a symmetric, ternary homopolymer-copolymer mixture: a Monte Carlo study. J Chem Phys. 105:1996;8885-8901.
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(1996)
J Chem Phys
, vol.105
, pp. 8885-8901
-
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Müller, M.1
Schick, M.2
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19
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0031548676
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The self-organisation of diblock copolymers at polymer blend interfaces
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Schnell R, Stamm M. The self-organisation of diblock copolymers at polymer blend interfaces. Physica B. 234:1997;247-249.
-
(1997)
Physica B
, vol.234
, pp. 247-249
-
-
Schnell, R.1
Stamm, M.2
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20
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0030195472
-
Homopolymer interfaces reinforced with random copolymers
-
of outstanding interest. Mechanical adhesion tests were combined with neutron reflectivity studies to provide a microscopic insight into the origin of the strengthening properties of random copolymers, and to rationalise the observed maximum in interfacial strength with copolymer composition.
-
Kulasekere R, Kaiser H, Ankner JF, Russell TP, Brown HR, Hawker CJ, Mayes AM. Homopolymer interfaces reinforced with random copolymers. of outstanding interest Macromolecules. 29:1996;5493-5496 Mechanical adhesion tests were combined with neutron reflectivity studies to provide a microscopic insight into the origin of the strengthening properties of random copolymers, and to rationalise the observed maximum in interfacial strength with copolymer composition.
-
(1996)
Macromolecules
, vol.29
, pp. 5493-5496
-
-
Kulasekere, R.1
Kaiser, H.2
Ankner, J.F.3
Russell, T.P.4
Brown, H.R.5
Hawker, C.J.6
Mayes, A.M.7
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21
-
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0030218412
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Microstructure of block copolymer reinforced interfaces observed with frictional force microscopy
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Jandt KD, Dai C-A, Kramer EJ. Microstructure of block copolymer reinforced interfaces observed with frictional force microscopy. Adv Mater. 8:1996;660-662.
-
(1996)
Adv Mater
, vol.8
, pp. 660-662
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Jandt, K.D.1
Dai C-A2
Kramer, E.J.3
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22
-
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0030190918
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Diblock copolymers as emulsifying agents in polymer blends: Influence of molecular weight, architecture, and chemical composition
-
of special interest. A systematic study of the effect of added diblock copolymers of different molecular weights and asymmetries and at different concentrations on the morphology of an immiscible polymer blend.
-
Cigana P, Favis BD, Jerome R. Diblock copolymers as emulsifying agents in polymer blends: influence of molecular weight, architecture, and chemical composition. of special interest J Polym Sci B. 34:1996;1691-1700 A systematic study of the effect of added diblock copolymers of different molecular weights and asymmetries and at different concentrations on the morphology of an immiscible polymer blend.
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(1996)
J Polym Sci B
, vol.34
, pp. 1691-1700
-
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Cigana, P.1
Favis, B.D.2
Jerome, R.3
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23
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0030378808
-
Interfacial modification of polymer blends - The emulsification curve: 2. Predicting the critical concentration of interfacial modifier from geometrical considerations
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Lomellini P, Matos M, Favis BD. Interfacial modification of polymer blends - the emulsification curve: 2. Predicting the critical concentration of interfacial modifier from geometrical considerations. Polymer. 37:1996;5689-5694.
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(1996)
Polymer
, vol.37
, pp. 5689-5694
-
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Lomellini, P.1
Matos, M.2
Favis, B.D.3
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24
-
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0030216741
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Compatibilisers for melt blending; Pre-made block copolymers
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of outstanding interest. An experimental study of the role of diblock copolymers in modifying the way morphology evolves during the melt blending of poly(methyl methacrylate) and polystyrene, focusing on the role of diblocks in modifying the coalescence process by imparting steric stabilisation to the dispersed phase droplets. Reference [25] reports work with similar conclusions.
-
Macosko CW, Guégan P, Khandpur AK. Compatibilisers for melt blending; pre-made block copolymers. of outstanding interest Macromolecules. 29:1996;5590-5598 An experimental study of the role of diblock copolymers in modifying the way morphology evolves during the melt blending of poly(methyl methacrylate) and polystyrene, focusing on the role of diblocks in modifying the coalescence process by imparting steric stabilisation to the dispersed phase droplets. Reference [25] reports work with similar conclusions.
-
(1996)
Macromolecules
, vol.29
, pp. 5590-5598
-
-
MacOsko, C.W.1
Guégan, P.2
Khandpur, A.K.3
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25
-
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0029673831
-
Coalescence in an interface-modified polymer blend as studied by light scattering measurements
-
of outstanding interest. The coalescence of particles in dispersions of poly(methyl methacrylate) in polystyrene under shear flow was studied in the presence of diblock copolymers. As in [24], the authors conclude that the major role of the diblocks is to inhibit coalescence by sterically stabilising the dispersed phase droplets, rather than in lowering the interfacial tension.
-
Snødergaard K, Lyngaae-Jørgenson J. Coalescence in an interface-modified polymer blend as studied by light scattering measurements. of outstanding interest Polymer. 37:1996;509-517 The coalescence of particles in dispersions of poly(methyl methacrylate) in polystyrene under shear flow was studied in the presence of diblock copolymers. As in [24], the authors conclude that the major role of the diblocks is to inhibit coalescence by sterically stabilising the dispersed phase droplets, rather than in lowering the interfacial tension.
-
(1996)
Polymer
, vol.37
, pp. 509-517
-
-
Snødergaard, K.1
Lyngaae-Jørgenson, J.2
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26
-
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0030192515
-
How copolymers promote mixing of immiscible materials
-
of outstanding interest. A theoretical rationale is developed for the view, expressed on the basis of experiments in references [24] and [25], that the major role of diblocks in modifying the morphology of immiscible blends is in inhibiting domain coalescence by steric stabilisation rather than lowering interfacial energy.
-
Milner ST, Xi H. How copolymers promote mixing of immiscible materials. of outstanding interest J Rheol. 40:1996;663-687 A theoretical rationale is developed for the view, expressed on the basis of experiments in references [24] and [25], that the major role of diblocks in modifying the morphology of immiscible blends is in inhibiting domain coalescence by steric stabilisation rather than lowering interfacial energy.
-
(1996)
J Rheol
, vol.40
, pp. 663-687
-
-
Milner, S.T.1
Xi, H.2
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27
-
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0025795469
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The adhesion between polymers
-
Brown HR. The adhesion between polymers. Annu Rev Mater Sci. 21:1991;463-489.
-
(1991)
Annu Rev Mater Sci
, vol.21
, pp. 463-489
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Brown, H.R.1
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28
-
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37049075680
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Strengthening polymer interfaces
-
Kramer EJ, Norton LJ, Dai C.-A., Sha Y, Hui C.-Y. Strengthening polymer interfaces. Faraday Discuss. 98:1994;31-46.
-
(1994)
Faraday Discuss
, vol.98
, pp. 31-46
-
-
Kramer, E.J.1
Norton, L.J.2
Dai, C.-A.3
Sha, Y.4
Hui, C.-Y.5
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29
-
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0031075892
-
Strengthening polymer interfaces with triblock copolymers
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Dai C-A, Jandt KD, Iyengar DR, Slack NL, Dai KH, Davidson WB, Kramer EJ. Strengthening polymer interfaces with triblock copolymers. Macromolecules. 30:1996;549-560.
-
(1996)
Macromolecules
, vol.30
, pp. 549-560
-
-
Dai C-A1
Jandt, K.D.2
Iyengar, D.R.3
Slack, N.L.4
Dai, K.H.5
Davidson, W.B.6
Kramer, E.J.7
-
30
-
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0030244272
-
Effect of ABC triblock copolymers with an elastomeric midblock on the adhesion between immiscible polymers
-
Brown HR, Krappe U, Stadler R. Effect of ABC triblock copolymers with an elastomeric midblock on the adhesion between immiscible polymers. Macromolecules. 29:1996;6582-6588.
-
(1996)
Macromolecules
, vol.29
, pp. 6582-6588
-
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Brown, H.R.1
Krappe, U.2
Stadler, R.3
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31
-
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0031075710
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Modifying a polystyrene/poly(methyl methacrylate) interface with poly (styrene-co-methyl methacrylate) random copolymers
-
of special interest. Mechanical measurements of the reinforcing action of random copolymers are combined with transmission electron microscopy, which shows that the random copolymer forms a separate phase at the interface.
-
Sikka M, Pellegrini NN, Schmitt EA, Winey KI. Modifying a polystyrene/poly(methyl methacrylate) interface with poly (styrene-co-methyl methacrylate) random copolymers. of special interest Macromolecules. 30:1997;445-455 Mechanical measurements of the reinforcing action of random copolymers are combined with transmission electron microscopy, which shows that the random copolymer forms a separate phase at the interface.
-
(1997)
Macromolecules
, vol.30
, pp. 445-455
-
-
Sikka, M.1
Pellegrini, N.N.2
Schmitt, E.A.3
Winey, K.I.4
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32
-
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0030569110
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Fracture toughness of polymer interface reinforced with diblock copolymer: Effect of homopolymer molecular weight
-
of special interest. Insight into the mechanisms of energy dissipation in copolymer reinforced interfaces is afforded by studying the dependence of interfacial on the entanglement properties of one of the homopolymers involved in the interface.
-
Dai C-A, Kramer EJ, Washiyama J, Hui C. Fracture toughness of polymer interface reinforced with diblock copolymer: effect of homopolymer molecular weight. of special interest Macromolecules. 29:1996;7536-7543 Insight into the mechanisms of energy dissipation in copolymer reinforced interfaces is afforded by studying the dependence of interfacial on the entanglement properties of one of the homopolymers involved in the interface.
-
(1996)
Macromolecules
, vol.29
, pp. 7536-7543
-
-
Dai C-A1
Kramer, E.J.2
Washiyama, J.3
Hui, C.4
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33
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3342964337
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Theory of chain pull-out and stability of weak interfaces. 2
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Kogan L, Hui C-Y, Ruina A. Theory of chain pull-out and stability of weak interfaces. 2. Macromolecules. 29:1996;4101-4106.
-
(1996)
Macromolecules
, vol.29
, pp. 4101-4106
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-
Kogan, L.1
Hui C-Y2
Ruina, A.3
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34
-
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0030146316
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Theory of chain pull-out and stability of weak interfaces. 1
-
Kogan L, Hui C-Y, Ruina A. Theory of chain pull-out and stability of weak interfaces. 1. Macromolecules. 29:1996;4090-4100.
-
(1996)
Macromolecules
, vol.29
, pp. 4090-4100
-
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Kogan, L.1
Hui C-Y2
Ruina, A.3
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35
-
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4243188122
-
Simulation of fracturing reinforced polymer blends
-
of outstanding interest. Brownian dynamics simulations were used to investigate molecular mechanisms of energy dissipation in copolymer reinforced interfaces; the results are that a chain that crosses the interface many times is much more efficient at strengthening an interface than one that crosses just once, such as a diblock copolymer.
-
Pickett GT, Jasnow D, Balazs AC. Simulation of fracturing reinforced polymer blends. of outstanding interest Phys Rev Lett. 77:1996;671-674 Brownian dynamics simulations were used to investigate molecular mechanisms of energy dissipation in copolymer reinforced interfaces; the results are that a chain that crosses the interface many times is much more efficient at strengthening an interface than one that crosses just once, such as a diblock copolymer.
-
(1996)
Phys Rev Lett
, vol.77
, pp. 671-674
-
-
Pickett, G.T.1
Jasnow, D.2
Balazs, A.C.3
-
36
-
-
0030193304
-
Polymer blends of PBT and PP compatibilised by ethylene-co-glycidyl methacrylate copolymers
-
Tsai CH, Chang FC. Polymer blends of PBT and PP compatibilised by ethylene-co-glycidyl methacrylate copolymers. J Appl Polym Sci. 61:1996;321-332.
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(1996)
J Appl Polym Sci
, vol.61
, pp. 321-332
-
-
Tsai, C.H.1
Chang, F.C.2
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37
-
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0031118718
-
Compatibilization mechanism of polymer blends with an in-situ compatibilizer
-
Kim JK, Kim S, Park CE. Compatibilization mechanism of polymer blends with an in-situ compatibilizer. Polymer. 38:1997;2155-2164.
-
(1997)
Polymer
, vol.38
, pp. 2155-2164
-
-
Kim, J.K.1
Kim, S.2
Park, C.E.3
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38
-
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0029714364
-
Compatibilising effect of a maleic anhydridge functionalised SEBS triblock elastomer through a reaction induced phase formation in the blends of polyamide-6 and polycarbonate. 1. Morphology and interfacial situation
-
Horiuchi S, Matchariyaku N, Yase K, Kitano T, Cho HK, Lee YM. Compatibilising effect of a maleic anhydridge functionalised SEBS triblock elastomer through a reaction induced phase formation in the blends of polyamide-6 and polycarbonate. 1. Morphology and interfacial situation. Polymer. 37:1996;3065-3078.
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(1996)
Polymer
, vol.37
, pp. 3065-3078
-
-
Horiuchi, S.1
Matchariyaku, N.2
Yase, K.3
Kitano, T.4
Cho, H.K.5
Lee, Y.M.6
-
39
-
-
0001337964
-
Polymer reaction kinetics at interfaces
-
of outstanding interest. The authors calculate the expected reaction rate for the grafting of long polymers at polymer/polymer interfaces. They find that high degrees of grafting are practically unattainable, because the grafting reaction becomes exponentially slow when the grafted chains start to strongly overlap. A corollary of this is that in practise large decreases in interfacial tension are unlikely to be attainable in practise, and steric stabilisation is likely to be responsible for most of the modifications of morphology obtainable by reactive compatibilisation.
-
O'Shaughnessy B, Sawhney U. Polymer reaction kinetics at interfaces. of outstanding interest Phys Rev Lett. 76:1996;3444-3447 The authors calculate the expected reaction rate for the grafting of long polymers at polymer/polymer interfaces. They find that high degrees of grafting are practically unattainable, because the grafting reaction becomes exponentially slow when the grafted chains start to strongly overlap. A corollary of this is that in practise large decreases in interfacial tension are unlikely to be attainable in practise, and steric stabilisation is likely to be responsible for most of the modifications of morphology obtainable by reactive compatibilisation.
-
(1996)
Phys Rev Lett
, vol.76
, pp. 3444-3447
-
-
O'Shaughnessy, B.1
Sawhney, U.2
-
40
-
-
0001414514
-
Diffusion controlled reactions at polymer-polymer interfaces
-
of outstanding interest. The authors calculate rate constants for the coupling of two long polymers at an interface to form a diblock copolymer, concentrating on the regime when the reaction is controlled by diffusion of the entangled species.
-
Fredrickson GH. Diffusion controlled reactions at polymer-polymer interfaces. of outstanding interest Phys Rev Lett. 76:1996;3440-3443 The authors calculate rate constants for the coupling of two long polymers at an interface to form a diblock copolymer, concentrating on the regime when the reaction is controlled by diffusion of the entangled species.
-
(1996)
Phys Rev Lett
, vol.76
, pp. 3440-3443
-
-
Fredrickson, G.H.1
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41
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0030569114
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Time-dependent reactive coupling at polymer-polymer interfaces
-
Fredrickson GH, Milner ST. Time-dependent reactive coupling at polymer-polymer interfaces. Macromolecules. 29:1996;7386-7390.
-
(1996)
Macromolecules
, vol.29
, pp. 7386-7390
-
-
Fredrickson, G.H.1
Milner, S.T.2
-
42
-
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0030192421
-
Reactive reinforcement of polystyrene/poly(2-vinyl pyridine) interfaces
-
of special interest. The effect of reactive compatibilisation at an interface on the adhesive properties of an interface was investigated by direct mechanical tests
-
Tan NCB, Pfeiffer DG, Briber RM. Reactive reinforcement of polystyrene/poly(2-vinyl pyridine) interfaces. of special interest Macromolecules. 29:1996;4969-4975 The effect of reactive compatibilisation at an interface on the adhesive properties of an interface was investigated by direct mechanical tests.
-
(1996)
Macromolecules
, vol.29
, pp. 4969-4975
-
-
Tan, N.C.B.1
Pfeiffer, D.G.2
Briber, R.M.3
-
43
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0030216185
-
Morphology control and interfacial reinforcement in reactive polystyrene/amorphous polyamide blends
-
Tan NCB, Tai S-K, Bribe RM. Morphology control and interfacial reinforcement in reactive polystyrene/amorphous polyamide blends. Polymer. 37:1996;3509-3519.
-
(1996)
Polymer
, vol.37
, pp. 3509-3519
-
-
Tan, N.C.B.1
Tai S-K2
Bribe, R.M.3
-
44
-
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0030171778
-
Fracture toughness and failure mechanisms of epoxy/rubber-modified polystyrene (HIPS) interfaces reinforced by grafted chains
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of special interest. The adhesion at an interface between high-impact polystyrene and epoxy was measured as a function of the amount of grafting of carboxylic-terminated polystyrene to the epoxy network, allowing a detailed picture of the relation between grafted chain length, grafting density and the fracture toughness to be built up.
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Sha Y, Hui CY, Kramer EJ, Hahn SF, Berglund CA. Fracture toughness and failure mechanisms of epoxy/rubber-modified polystyrene (HIPS) interfaces reinforced by grafted chains. of special interest Macromolecules. 29:1996;4728-4736 The adhesion at an interface between high-impact polystyrene and epoxy was measured as a function of the amount of grafting of carboxylic-terminated polystyrene to the epoxy network, allowing a detailed picture of the relation between grafted chain length, grafting density and the fracture toughness to be built up.
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(1996)
Macromolecules
, vol.29
, pp. 4728-4736
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Sha, Y.1
Hui, C.Y.2
Kramer, E.J.3
Hahn, S.F.4
Berglund, C.A.5
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45
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0001722331
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Effects of the formation of copolymer on the interfacial adhesion between semicrystalline polymers
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of outstanding interest. A direct relationship was found between the amount of diblock copolymer formed in situ, by grafting at an interface between polypropylene and polyamide-6, and the fracture toughness of the interface. This relationship, quadratic in the areal density of copolymer, is the same as found previously for the toughness of interface between glassy polymers modified by added diblocks.
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Boucher E, Folkers JP, Hervet H, Léger L, Creton C. Effects of the formation of copolymer on the interfacial adhesion between semicrystalline polymers. of outstanding interest Macromolecules. 29:1996;774-782 A direct relationship was found between the amount of diblock copolymer formed in situ, by grafting at an interface between polypropylene and polyamide-6, and the fracture toughness of the interface. This relationship, quadratic in the areal density of copolymer, is the same as found previously for the toughness of interface between glassy polymers modified by added diblocks.
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(1996)
Macromolecules
, vol.29
, pp. 774-782
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Boucher, E.1
Folkers, J.P.2
Hervet, H.3
Léger, L.4
Creton, C.5
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46
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0031557621
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Enhanced adhesion between polypropylene and polyamide-6: Role of interfacial nucleation of the beta-crystalline form of polypropylene
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Boucher E, Folkers JP, Creton C, Hervet H, Léger L. Enhanced adhesion between polypropylene and polyamide-6: role of interfacial nucleation of the beta-crystalline form of polypropylene. Macromolecules. 30:1997;2102-2109.
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(1997)
Macromolecules
, vol.30
, pp. 2102-2109
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Boucher, E.1
Folkers, J.P.2
Creton, C.3
Hervet, H.4
Léger, L.5
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