-
4
-
-
0036722050
-
-
M. Rätzsch, M. Arnold, E. Borsig, H. Bucka, and N. Reichelt Prog Polym Sci 27 2002 1195 1282
-
(2002)
Prog Polym Sci
, vol.27
, pp. 1195-1282
-
-
Rätzsch, M.1
Arnold, M.2
Borsig, E.3
Bucka, H.4
Reichelt, N.5
-
7
-
-
34547253243
-
-
T.J. McCallum, M. Kontopoulou, C.B. Park, E.B. Muliawan, and S.G. Hatzikiriakos Polym Eng Sci 42 2007 1133 1140
-
(2007)
Polym Eng Sci
, vol.42
, pp. 1133-1140
-
-
McCallum, T.J.1
Kontopoulou, M.2
Park, C.B.3
Muliawan, E.B.4
Hatzikiriakos, S.G.5
-
8
-
-
0001763308
-
-
S. Kurzbeck, F. Oster, H. Munstedt, T.Q. Nguyen, and R. Gensler J Rheol 43 1999 359 374
-
(1999)
J Rheol
, vol.43
, pp. 359-374
-
-
Kurzbeck, S.1
Oster, F.2
Munstedt, H.3
Nguyen, T.Q.4
Gensler, R.5
-
14
-
-
34247579578
-
-
J.A. Langston, R.H. Colby, T.C.M. Chung, U.V. Park, V. Pennsyl, and F. Shimizu Macromolecules 40 2007 2712 2720
-
(2007)
Macromolecules
, vol.40
, pp. 2712-2720
-
-
Langston, J.A.1
Colby, R.H.2
Chung, T.C.M.3
Park, U.V.4
Pennsyl, V.5
Shimizu, F.6
-
15
-
-
0037754343
-
-
U. S Patent 5554668
-
Scheve, J. B.; Mayfield, J. W.; DeNicola, A. J. J. High melt strength, propylene polymer, process for making it, and use thereof. U. S Patent 5554668. 1996.
-
(1996)
High Melt Strength, Propylene Polymer, Process for Making It, and Use Thereof
-
-
Scheve, J.B.1
Mayfield, J.W.2
Denicola, A.J.J.3
-
16
-
-
74449083872
-
-
H. Otaguro, L.F.C.P. de Lima, D.F. Parra, A.B. Lugão, M.A. Chinelatto, and S.V. Canevarolo Radiat Phys Chem 79 2010 318 324
-
(2010)
Radiat Phys Chem
, vol.79
, pp. 318-324
-
-
Otaguro, H.1
De Lima, L.F.C.P.2
Parra, D.F.3
Lugão, A.B.4
Chinelatto, M.A.5
Canevarolo, S.V.6
-
17
-
-
10844234985
-
-
D. Auhl, J. Stange, H. Münstedt, B. Krause, D. Voigt, and A. Lederer Macromolecules 37 2004 9465 9472
-
(2004)
Macromolecules
, vol.37
, pp. 9465-9472
-
-
Auhl, D.1
Stange, J.2
Münstedt, H.3
Krause, B.4
Voigt, D.5
Lederer, A.6
-
18
-
-
0001606754
-
-
M. Sugimoto, T. Tanaka, Y. Masubuchi, J. Takimoto, and K. Koyama J Appl Polym Sci 73 1999 1493 1500
-
(1999)
J Appl Polym Sci
, vol.73
, pp. 1493-1500
-
-
Sugimoto, M.1
Tanaka, T.2
Masubuchi, Y.3
Takimoto, J.4
Koyama, K.5
-
19
-
-
0030126023
-
-
F. Yoshii, K. Makuuchi, S. Kikukawa, T. Tanaka, J. Saitoh, and K. Koyama J Appl Polym Sci 60 1996 617 623
-
(1996)
J Appl Polym Sci
, vol.60
, pp. 617-623
-
-
Yoshii, F.1
Makuuchi, K.2
Kikukawa, S.3
Tanaka, T.4
Saitoh, J.5
Koyama, K.6
-
20
-
-
36148991815
-
-
H. Otaguro, S.O. Rogero, A. Yoshiga, L.F.C.P. Lima, D.F. Parra, and B.W.H. Artel Nucl Instrum Methods B 265 2007 232 237
-
(2007)
Nucl Instrum Methods B
, vol.265
, pp. 232-237
-
-
Otaguro, H.1
Rogero, S.O.2
Yoshiga, A.3
Lima, L.F.C.P.4
Parra, D.F.5
Artel, B.W.H.6
-
21
-
-
68449084435
-
-
A. Yoshiga, H. Otaguro, D.F. Parra, L.F.C.P. Lima, and A.B. Lugao Polym Bull 63 2009 397 409
-
(2009)
Polym Bull
, vol.63
, pp. 397-409
-
-
Yoshiga, A.1
Otaguro, H.2
Parra, D.F.3
Lima, L.F.C.P.4
Lugao, A.B.5
-
25
-
-
82755161907
-
-
D. Wan, L. Ma, Z. Zhang, H. Xing, L. Wang, and Z. Jiang Polym Degrad Stab 97 2012 40 48
-
(2012)
Polym Degrad Stab
, vol.97
, pp. 40-48
-
-
Wan, D.1
Ma, L.2
Zhang, Z.3
Xing, H.4
Wang, L.5
Jiang, Z.6
-
32
-
-
79957909615
-
-
K. Cao, Y. Li, Z. Lu, S.-L. Wu, Z. Chen, and Z. Yao J Appl Polym Sci 121 2011 3384 3392
-
(2011)
J Appl Polym Sci
, vol.121
, pp. 3384-3392
-
-
Cao, K.1
Li, Y.2
Lu, Z.3
Wu, S.-L.4
Chen, Z.5
Yao, Z.6
-
33
-
-
84879025825
-
-
Y. Li, Z. Yao, Z. Chen, S. Qiu, C. Zeng, and K. Cao Ind Eng Chem Res 52 2013 7758 7767
-
(2013)
Ind Eng Chem Res
, vol.52
, pp. 7758-7767
-
-
Li, Y.1
Yao, Z.2
Chen, Z.3
Qiu, S.4
Zeng, C.5
Cao, K.6
-
40
-
-
0033136523
-
-
Q. Yu, and S. Zhu Polymer 40 1999 2961 2968
-
(1999)
Polymer
, vol.40
, pp. 2961-2968
-
-
Yu, Q.1
Zhu, S.2
-
42
-
-
0003451399
-
-
Induced decomposition of BPO can occur when a benzoate radical (resulting from either spontaneous decomposition or induced decomposition of BPO) reacts with BPO to yield carbon dioxide, phenyl benzoate, and a benzoate radical. Consequently, induced decomposition increases with increasing BPO concentration and results in loss of reactivity of radicals that would otherwise be produced from the spontaneous decomposition of BPO. See
-
Induced decomposition of BPO can occur when a benzoate radical (resulting from either spontaneous decomposition or induced decomposition of BPO) reacts with BPO to yield carbon dioxide, phenyl benzoate, and a benzoate radical. Consequently, induced decomposition increases with increasing BPO concentration and results in loss of reactivity of radicals that would otherwise be produced from the spontaneous decomposition of BPO. See K. Nozaki, and P.D. Bartlett J Am Chem Soc 68 1946 1686 1692
-
(1946)
J Am Chem Soc
, vol.68
, pp. 1686-1692
-
-
Nozaki, K.1
Bartlett, P.D.2
-
45
-
-
84961344284
-
-
Akzo Nobel N.V. [accessed 17.08.14]
-
Akzo Nobel N.V. High melt strength polypropylene https://www.akzonobel.com/polymer/your-industry/polymer-modification/high-meltstrength-polypropylene-hmspp/ [accessed 17.08.14].
-
High Melt Strength Polypropylene
-
-
-
53
-
-
41749113310
-
-
K. Wakabayashi, C. Pierre, D.A. Dikin, R.S. Ruoff, T. Ramanathan, and L.C. Brinson Macromolecules 41 2008 1905 1908
-
(2008)
Macromolecules
, vol.41
, pp. 1905-1908
-
-
Wakabayashi, K.1
Pierre, C.2
Dikin, D.A.3
Ruoff, R.S.4
Ramanathan, T.5
Brinson, L.C.6
-
54
-
-
77958173712
-
-
K. Wakabayashi, P.J. Brunner, J. Masuda, S.A. Hewlett, and J.M. Torkelson Polymer 51 2010 5525 5531
-
(2010)
Polymer
, vol.51
, pp. 5525-5531
-
-
Wakabayashi, K.1
Brunner, P.J.2
Masuda, J.3
Hewlett, S.A.4
Torkelson, J.M.5
-
67
-
-
0342561645
-
-
K. Jordens, G.L. Wilkes, J. Janzen, D.C. Rohlfing, and M.B. Welch Polymer 41 2000 7175 7192
-
(2000)
Polymer
, vol.41
, pp. 7175-7192
-
-
Jordens, K.1
Wilkes, G.L.2
Janzen, J.3
Rohlfing, D.C.4
Welch, M.B.5
-
77
-
-
0037046352
-
-
D.J. Lohse, S.T. Milner, L.J. Fetters, M. Xenidou, N. Hadjichristidis, and R.A. Mendelson Macromolecules 35 2002 3066 3075
-
(2002)
Macromolecules
, vol.35
, pp. 3066-3075
-
-
Lohse, D.J.1
Milner, S.T.2
Fetters, L.J.3
Xenidou, M.4
Hadjichristidis, N.5
Mendelson, R.A.6
-
78
-
-
79958800805
-
-
L. Wang, D. Wan, Z. Zhang, F. Liu, H. Xing, and Y. Wang Macromolecules 44 2011 4167 4179
-
(2011)
Macromolecules
, vol.44
, pp. 4167-4179
-
-
Wang, L.1
Wan, D.2
Zhang, Z.3
Liu, F.4
Xing, H.5
Wang, Y.6
-
79
-
-
70449499085
-
-
S. Li, M. Xiao, D. Wei, H. Xiao, F. Hu, and A. Zheng Polymer 50 2009 6121 6128
-
(2009)
Polymer
, vol.50
, pp. 6121-6128
-
-
Li, S.1
Xiao, M.2
Wei, D.3
Xiao, H.4
Hu, F.5
Zheng, A.6
-
81
-
-
84878993117
-
-
M. Zhang, R.H. Colby, S.T. Milner, T.C.M. Chung, T. Huang, and A.W. DeGroot Macromolecules 46 2013 4313 4323
-
(2013)
Macromolecules
, vol.46
, pp. 4313-4323
-
-
Zhang, M.1
Colby, R.H.2
Milner, S.T.3
Chung, T.C.M.4
Huang, T.5
Degroot, A.W.6
-
85
-
-
34547111261
-
-
We discount the possibility of branching by bimolecular ester-ester reactions resulting in formation of an ether with water as side product during SSSP or melt extrusion because such reactions have not been described in the literature. Instead, preparation of ethers from esters generally is done by direct reduction of the carbonyl group of esters. See, for example, [and references therein]
-
We discount the possibility of branching by bimolecular ester-ester reactions resulting in formation of an ether with water as side product during SSSP or melt extrusion because such reactions have not been described in the literature. Instead, preparation of ethers from esters generally is done by direct reduction of the carbonyl group of esters. See, for example N. Sakai, T. Moriya, and T. Konakahara J Org Chem 72 2007 5920 5922 [and references therein]
-
(2007)
J Org Chem
, vol.72
, pp. 5920-5922
-
-
Sakai, N.1
Moriya, T.2
Konakahara, T.3
-
88
-
-
0141975263
-
-
S. Camera, B.C. Gilbert, R.J. Meier, M. van Duin, and A.C. Whitwood Org Biomol Chem 1 2003 1181 1190
-
(2003)
Org Biomol Chem
, vol.1
, pp. 1181-1190
-
-
Camera, S.1
Gilbert, B.C.2
Meier, R.J.3
Van Duin, M.4
Whitwood, A.C.5
-
92
-
-
0034300776
-
-
M. Lazár, L. Hrckova, E. Borsig, A. Marcincin, N. Reichelt, and M. Rätzsch J Appl Polym Sci 78 2000 886 893
-
(2000)
J Appl Polym Sci
, vol.78
, pp. 886-893
-
-
Lazár, M.1
Hrckova, L.2
Borsig, E.3
Marcincin, A.4
Reichelt, N.5
Rätzsch, M.6
-
94
-
-
84885223883
-
-
The residual BPO content was determined using information about the grafting yeild obtained for each sample and reported in Ref. [57] The calculations were based on the assumptions that all PP macroradicals were formed solely by chain transfer with BPO radicals and that no induced decomposition of BPO occurs
-
The residual BPO content was determined using information about the grafting yeild obtained for each sample and reported in Ref. [57] M.F. Diop, and J.M. Torkelson Macromolecules 46 2013 7834 7844 The calculations were based on the assumptions that all PP macroradicals were formed solely by chain transfer with BPO radicals and that no induced decomposition of BPO occurs
-
(2013)
Macromolecules
, vol.46
, pp. 7834-7844
-
-
Diop, M.F.1
Torkelson, J.M.2
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