Studies on bismaleimides and related materials: 1. D.m.t.a. investigation of the reaction of bismaleimides with m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide: an approach to the design of novel reactive diluents

G. Davidson; I. Soutar; P. N. Preston; V. K. Shah; S. W. Simpson; N. J. Stewart

Studies on bismaleimides and related materials: 1. D.m.t.a. investigation of the reaction of bismaleimides with m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide: an approach to the design of novel reactive diluents

G. Davidson, I. Soutar, P. N. Preston, V. K. Shah, S. W. Simpson, N. J. Stewart

School of Engineering & Physical Sciences

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

Abstract

Dynamic mechanical thermal analysis (d.m.t.a.) profiles have been recorded for interaction of m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide with the bismaleimide (BMI) derived from 3,3-diaminobenzophenone. Additional chemical events for each system are recognized at temperatures below the conventional BMI curing region. Resins prepared from the BMI/azine and BMI N-oxide systems have lower thermal stability than the neat resin but differences are moderate at low additive concentrations. © 1994.

Original language	English
Pages (from-to)	653-657
Number of pages	5
Journal	Polymer
Volume	35
Issue number	3
Publication status	Published - Feb 1994

Keywords

azine
bismaleimide
heteroaromatic N-oxide

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@article{1adb686b4855400d85e73a13a3ce9c88,

title = "Studies on bismaleimides and related materials: 1. D.m.t.a. investigation of the reaction of bismaleimides with m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide: an approach to the design of novel reactive diluents",

abstract = "Dynamic mechanical thermal analysis (d.m.t.a.) profiles have been recorded for interaction of m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide with the bismaleimide (BMI) derived from 3,3-diaminobenzophenone. Additional chemical events for each system are recognized at temperatures below the conventional BMI curing region. Resins prepared from the BMI/azine and BMI N-oxide systems have lower thermal stability than the neat resin but differences are moderate at low additive concentrations. {\textcopyright} 1994.",

keywords = "azine, bismaleimide, heteroaromatic N-oxide",

author = "G. Davidson and I. Soutar and Preston, \{P. N.\} and Shah, \{V. K.\} and Simpson, \{S. W.\} and Stewart, \{N. J.\}",

year = "1994",

month = feb,

language = "English",

volume = "35",

pages = "653--657",

journal = "Polymer",

issn = "0032-3861",

publisher = "Elsevier B.V.",

number = "3",

}

Studies on bismaleimides and related materials: 1. D.m.t.a. investigation of the reaction of bismaleimides with m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide: an approach to the design of novel reactive diluents. / Davidson, G.; Soutar, I.; Preston, P. N. et al.
In: Polymer, Vol. 35, No. 3, 02.1994, p. 653-657.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Studies on bismaleimides and related materials

T2 - 1. D.m.t.a. investigation of the reaction of bismaleimides with m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide: an approach to the design of novel reactive diluents

AU - Davidson, G.

AU - Soutar, I.

AU - Preston, P. N.

AU - Shah, V. K.

AU - Simpson, S. W.

AU - Stewart, N. J.

PY - 1994/2

Y1 - 1994/2

N2 - Dynamic mechanical thermal analysis (d.m.t.a.) profiles have been recorded for interaction of m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide with the bismaleimide (BMI) derived from 3,3-diaminobenzophenone. Additional chemical events for each system are recognized at temperatures below the conventional BMI curing region. Resins prepared from the BMI/azine and BMI N-oxide systems have lower thermal stability than the neat resin but differences are moderate at low additive concentrations. © 1994.

AB - Dynamic mechanical thermal analysis (d.m.t.a.) profiles have been recorded for interaction of m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide with the bismaleimide (BMI) derived from 3,3-diaminobenzophenone. Additional chemical events for each system are recognized at temperatures below the conventional BMI curing region. Resins prepared from the BMI/azine and BMI N-oxide systems have lower thermal stability than the neat resin but differences are moderate at low additive concentrations. © 1994.

KW - azine

KW - bismaleimide

KW - heteroaromatic N-oxide

UR - https://www.scopus.com/pages/publications/0345529373

M3 - Article

SN - 0032-3861

VL - 35

SP - 653

EP - 657

JO - Polymer

JF - Polymer

IS - 3

ER -

Studies on bismaleimides and related materials: 1. D.m.t.a. investigation of the reaction of bismaleimides with m-tolualdehyde azine and 3,5-dimethylpyridine N-oxide: an approach to the design of novel reactive diluents

Abstract

Keywords

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