A reactive melt modification of polyethylene terephthalate

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8 enough for controlled biaxial stretching to take place which limits its melt processing applications. It should be noted that, in the case of PET filaments, despite the low melt strength, sagging does not arise because the filament is formed by accelerating the melt in the direction of gravity (Gupta and Bashir, 2002).
9 In the case of sheet applications, the amorphous PET sheet is made by extruding an appropriate molecular weight PET melt through a slit die and quenching over a chill roller (Dealy and Wissbrun, 1990). In thermoforming, the PET sheet is reheated or softened above Tg, but below the cold crystallization temperature A ce , and cold molds are used to make clear cups, trays and blister packages for pharmaceutical tablets (Gupta and Bashir, 2002). Biaxially oriented thin films (5-180pm) are made from PET in a sequential drawing process (Gupta and Bashir, 2002). In this process, PET is melt extruded through a slit die and quenched to form an amorphous precursor film. The quenched film is later drawn in the extrusion direction and the tangential direction. The films prepared under clean room conditions are used in applications such as video and magnetic tapes, floppy disks, photographic products, and capacitors. Biaxially oriented thick films (75-180lim) are used in photographic applications. The PET resins produced by conventional synthetic routes are suitable for a variety of applications and end uses. However, their particular macromolecular structures may raise unique rheological concerns regarding their broader range of applications. For example, linear PET synthesized as described before in Section 1.1, if processed for applications involving extrusion foaming to low densities, extrusion blow molding, and thermoforming operations may present limitations mainly through its inadequate rheological properties for such operations.
Page 1 and 2: Copyright Warning & Restrictions Th
Page 3 and 4: ABSTRACT REACTIVE MELT MODIFICATION
Page 5 and 6: REACTIVE MELT MODIFICATION OF POLYE
Page 7 and 8: BIOGRAPHICAL SKETCH Author: Rahul R
Page 9 and 10: Copyright © 2003 by Rahul Ramesh D
Page 11 and 12: ACKNOWLEDGEMENTS I always considere
Page 13 and 14: TABLE OF CONTENTS Chapter Page 1 IN
Page 15 and 16: TABLE OF CONTENTS (Continued) Chapt
Page 17 and 18: LIST OF FIGURES Figure Page 1.1 Mac
Page 19 and 20: LIST OF FIGURES (Continued) Figure
Page 21 and 22: LIST OF FIGURES (Continued) Figure
Page 23 and 24: Striation Thickness Time Diffusion
Page 25 and 26: tertiary amine terephthalic acid th
Page 27 and 28: CHAPTER 1 INTRODUCTION After its in
Page 29 and 30: 3 of 0.5-1.00 mm Hg (Sorenson 2001)
Page 31 and 32: where rib is the solution viscosity
Page 33: 7 are not suitable for most of the
Page 37 and 38: 11 operation (Dealy and Wissbrun, 1
Page 39 and 40: 13 During the cell growth phase of
Page 41 and 42: 15 suitability of extruders as cont
Page 43 and 44: 17 conditions and additive concentr
Page 45 and 46: 19 understand the effect of evolvin
Page 47 and 48: CHAPTER 3 LITERATURE REVIEW This ch
Page 49 and 50: 23 absence of modifiers is accompan
Page 51 and 52: 25 The primary objective while modi
Page 53 and 54: 27 Polypropylene resins with high m
Page 55 and 56: 29 initially the reaction with hydr
Page 57 and 58: 31 A diglycidyl ether, often in the
Page 59 and 60: 33 Characterizing the products of t
Page 61 and 62: 35 5. Ease of mixing in the polymer
Page 63 and 64: 37 Figure 3.4 Epoxy or 0xirane ring
Page 65 and 66: 39 carbocation stability overrides
Page 67 and 68: 41 Figure 3.9 Anhydride — epoxy r
Page 69 and 70: 43 Figure 3.12 Base catalyzed hydro
Page 71 and 72: 45 activity to enhance the PET-epox
Page 73 and 74: 47 4.1.2 Chain EDtenders The struct
Page 75 and 76: TGDDM was used in the batch mixer s
Page 77 and 78: 51 4.2 Processing and Characterizat
Page 79 and 80: 53 specimens as a function of freVu
Page 81 and 82: 55 to the parallel plates). An addi
Page 83 and 84: 57 background spectrum. It took app
Page 85 and 86:
CHAPTER 5 RESULTS AND DISCUSSION Th
Page 87 and 88:
61 molecular weight of MPET as also
Page 89 and 90:
63 rate expressions analogous to th
Page 91 and 92:
Figure 5.5 Possible reactions betwe
Page 93 and 94:
67 taking place by the convective;
Page 95 and 96:
69 5.1.4 Comparison of Epoxides Fig
Page 97 and 98:
71 5.1.5 Reactions of TGIC with HPE
Page 99 and 100:
73 Figure 5.11 shows the vanation o
Page 101 and 102:
75 Figure 5.13 shows the effect of
Page 103 and 104:
77 to time. In a general sense, the
Page 105 and 106:
79 5.1.7 Study on Role of Catalysts
Page 107 and 108:
81 groups adjacent to the tertiary
Page 109 and 110:
83 overall less activity towards TG
Page 111 and 112:
85 5.2.1 Typical Batch MiDing Runs
Page 113 and 114:
87 It appears that the higher proce
Page 115 and 116:
89 injection (Dealy and Wissbrun, 1
Page 117 and 118:
91 rheological power scaling law fo
Page 119 and 120:
93 In the calculations, the freVuen
Page 121 and 122:
95 whereas H(?.) of the unmodified
Page 123 and 124:
97 However, the disintegration of t
Page 125 and 126:
99 the Section 4.1.3. As evident fr
Page 127 and 128:
101 changes in dynamic moduli and m
Page 129 and 130:
103 In the case of 270 °C, the mod
Page 131 and 132:
105 accessibility of unreacted grou
Page 133 and 134:
107 believed to be charactenzed by
Page 135 and 136:
109 increase in the melt elasticity
Page 137 and 138:
111 In general, for crosslinked sys
Page 139 and 140:
113 crosslinked gels in swelling eV
Page 141 and 142:
115 formation of epoxy/PET reaction
Page 143 and 144:
117 A seVuential reactive extrusion
Page 145 and 146:
CHAPTER 6 CONCLUSIONS AND RECOMMEND
Page 147 and 148:
121 of PET by the selected tnepoxid
Page 149 and 150:
REFERENCES S. Abe and M. Yamaguchi,
Page 151 and 152:
125 L. M. Dossin and W. W. Graessle
Page 153 and 154:
127 P. Huang, Z. Zhong, S. Zheng, W
Page 155 and 156:
129 J. Meissner and J. Hostettler,
Page 157 and 158:
131 T. Shiwaku, K. Hijikata, K. Fur
Page 159 and 160:
133 M. Xanthos and S. K. Dey, "Foam
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A reactive melt modification of polyethylene terephthalate

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