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11. |
Use of DTA with infrared analysis of evolved gas to investigate the effect of flame retardants on gas evolution from pyrolysed cellulose (cotton) |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 61-67
Dennis Price,
A. R. (Dick) Horrocks,
Mehmet Akalin,
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摘要:
AbstractDTA combined with infrared analysis of the evolved gas (EGA) has been used to study the temperature behaviour, both in air and nitrogen, of commercial phosphorus‐ and nitrogen‐ and/or bromine‐containing flame retardants applied to cotton. By reference to the DTA traces and also the maxima occurring in the CO, CO2and H2O evolution rates, seven significant peak temperatures were assigned. Two new relatively low temperature peaks have been observed: the higher of these is DTA‐sensitive and occurs in all unretarded and retarded samples and is ascribed to the formation of an ‘activated cellulose’ state previously proposed by Bradbury, Sakai and Shafizadeh;17the lower peak is an exotherm (188‐220°C) associated with H2O and CO2evolution from flame‐retarded samples only. These observations are interpreted in terms of the mechanism of the cellulose pyrolysis/combustion and the influence of the
ISSN:0007-1641
DOI:10.1002/pi.4980200112
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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12. |
Synthesis and characterisation of poly(arylene sulphides): Part 10. A comparative evaluation of the thermoanalytical behaviour and curing of poly(1,4‐phenylene sulphide) and copolymers containing 1,4‐phenylene sulphide and 2‐methyl‐1,4‐phenylene sulphide repeat units |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 69-75
Peter A. Lovell,
Richard H. Still,
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摘要:
AbstractThermogravimetry, differential scanning calorimetry and curing studies were used to assess the viability of random and block copolymers comprising 1,4‐phenylene sulphide and 2‐methyl‐1,4‐phenylene sulphide repeat units as alternatives to poly(1,4‐phenylene sulphide) (PPS). The properties of the copolymers are discussed critically and compared with those of the parent homopolymers PPS and poly(2‐methyl‐1,4‐phenylene sulphide) (PMPS). The results suggest that (a) random copolymers with low PMPS contents would offer the best compromise between PPS and PMPS properties, and (b) more desirable physical properties might be achieved from systems containing a less reactive 2‐substituted‐1,4‐phenylene sulphide
ISSN:0007-1641
DOI:10.1002/pi.4980200113
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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13. |
Application of thermal methods in the characterisation of poly(urethane‐urea)s formed by reaction injection moulding |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 77-83
Anthony J. Ryan,
John L. Stanford,
Richard H. Still,
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摘要:
AbstractDifferential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) have been used in conjunction with tensile testing and transmission electron microscopy (TEM) to characterise novel segmented poly(urethane‐urea) (PUU) network materials formed by reaction injection moulding (RIM).Materials were based on a modified liquid 4,4′‐diphenylmethane diisocyanate and a polyether triol in admixture with one of three hindered aromatic diamines: 3,5‐diethyltoluene diamine (DETDA); methylene‐bis‐2,6‐diisopropylaniline (MMIPA); methylene‐bis‐(2‐methyl‐6‐isopropylaniline) (MMIPA).The materials ranged from tough translucent elastomers to opaque brittle plastics depending on the chemical nature and weight fraction of the hard segments (HS). DSC and DMTA studies showed the PUU materials to be phase‐separated; this was confirmed by TEM and tensile testing. The soft‐segment glass transition temperatures (DSC and DMTA) were independent of composition but varied with diamine structure. Hard‐segment glass transition temperatures could only be evaluated by DMTA and no evidence of crystallinity was found by thermal methods or by wide angle x‐ray diffraction. Heat capacity measurements and DMTA suggested that some degree of phase mixing had occurred, to a greater extent in the DETDA and MDIPA systems.Phase inversion was observed by DMTA and confirmed at ∼55% hard‐segment content f
ISSN:0007-1641
DOI:10.1002/pi.4980200114
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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14. |
Computer applications in the polymer laboratory edited by T. Provdcr, ACS Symposium Series No. 313, American Chemical Society, Washington DC, 1986. pp. x + 323, price $69.95 (USA&Canada), $83.95 (rest of world). ISBN 0‐8412‐0977‐4 |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 85-86
R. G. Linford,
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ISSN:0007-1641
DOI:10.1002/pi.4980200117
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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15. |
Catalytical and radical polymerization (advances in polymer science, volume 8 I), Springer‐Verlag, Berlin, Heidelberg, New York, London, Paris, Tokyo, 1986. pp. x + 240, price DM 148.00. ISBN 0‐540‐16754‐4 |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 86-87
A. D. Jenkins,
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ISSN:0007-1641
DOI:10.1002/pi.4980200119
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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16. |
High performance polymers: Their origin and development edited by R. B. Seymour and G. S. Kirshenbaum, Elscvicr Science Publishing Co. Inc., New York, 1986. pp. xiii +461, price £55.00. ISBN 0‐4440‐ 1 139‐0 |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 87-88
C. A. Finch,
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ISSN:0007-1641
DOI:10.1002/pi.4980200121
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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17. |
Future trends in polymer science and technology‐polymers: Commodities or specialities? edited by E. Martuscelli, C. Marchetta and L. Nicolais, Technomic Publishing AG, Basel, 1987. pp. vii + 247, pricc SwFr 98.00. ISBN 0‐87762‐512‐3 |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 88-88
C. A. Finch,
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ISSN:0007-1641
DOI:10.1002/pi.4980200124
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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18. |
Calendar of meetings |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page 89-90
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ISSN:0007-1641
DOI:10.1002/pi.4980200125
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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19. |
Masthead |
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British Polymer Journal,
Volume 20,
Issue 1,
1988,
Page -
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ISSN:0007-1641
DOI:10.1002/pi.4980200101
出版商:John Wiley&Sons, Ltd
年代:1988
数据来源: WILEY
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