2004
DOI: 10.1016/j.tca.2004.01.012
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Analysis of the area of material really tested by TMA

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Cited by 7 publications
(9 citation statements)
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“…However, little is known about the usability of these characteristics to optimize the composite formulation and processing parameters. It is due to several factors: TMA tests concern surface layers up to 0.5 mm thick,14 whereas in mechanical measurements, a specimen is usually much thicker depending on the test. This fact influences the gradient of crosslink density of the specimen and both the gradient of crystallinity degree and crystals' sizes distribution if the material is crystallizable.…”
Section: Methodsmentioning
confidence: 99%
“…However, little is known about the usability of these characteristics to optimize the composite formulation and processing parameters. It is due to several factors: TMA tests concern surface layers up to 0.5 mm thick,14 whereas in mechanical measurements, a specimen is usually much thicker depending on the test. This fact influences the gradient of crosslink density of the specimen and both the gradient of crystallinity degree and crystals' sizes distribution if the material is crystallizable.…”
Section: Methodsmentioning
confidence: 99%
“…14 and Table III). The α 2 /α 1 ratio of thermal expansion coefficients in rubbery and glassy state is between 2.5 and 5.12 and it is characteristic for amorphous materials 38, 42…”
Section: Resultsmentioning
confidence: 99%
“…Simultaneously, evaluation of the compaction factor $ V_c^{{\rm{TMA}}} \approx 3\left({\alpha _{\rm{1}}-\alpha _{\rm{2}}}\right) $ T g could be done,39–41 where α 1 is the coefficient of linear thermal expansion in a glassy state = (Δ H / H o )/Δ T , where Δ H / H o is a relative change in the initial height H o (specimen thickness) within the temperature interval, Δ T , α 2 —as α 1 but in a rubbery state. However, usability of these characteristics for optimizing the composite formulation and processing parameters is limited due to several factors: First, TMA tests a surface layer up to 0.5 mm thick42 when in mechanical measurements a specimen is usually much thicker depending on which test is considered. This fact influences the gradient of all crosslink density of specimen, crystallinity degree and crystals' sizes distribution while the material is crystallizable.…”
Section: Methodsmentioning
confidence: 99%
“…The technique is based on the measurement of sample deformation under very low load as the temperature is increased and two main modes of deformation, defined by the probe/sample contact area and the applied load, can be performed: (i) expansion, when low forces are applied to large contact areas, and (ii) penetration, with small contact areas and high forces. [1][2][3][4][5] In general, a combination of expansion/penetration is observed. TMA has been used successfully for the measurement of several properties of polymers, such as the glass transition temperature, 1,3,4 softening temperature, 1,2,4 thermal expansion coefficient, 1,2,6 degree of crosslinking 1,2,7 and the average number of degrees of freedom of polymer segments between crosslinks.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5] In general, a combination of expansion/penetration is observed. TMA has been used successfully for the measurement of several properties of polymers, such as the glass transition temperature, 1,3,4 softening temperature, 1,2,4 thermal expansion coefficient, 1,2,6 degree of crosslinking 1,2,7 and the average number of degrees of freedom of polymer segments between crosslinks. 8 A transition temperature is generally taken as a temperature at which the rate or direction of probe deflection changes abruptly.…”
Section: Introductionmentioning
confidence: 99%