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VISCOSITY‐TIME‐TEMPERATURE RELATIONS IN GLASS AT ANNEALING TEMPERATURES *
Author(s) -
Lillie Howard R.
Publication year - 1933
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1151-2916.1933.tb19269.x
Subject(s) - thermodynamics , viscosity , annealing (glass) , glass transition , chemistry , temperature dependence of liquid viscosity , relative viscosity , materials science , mineralogy , polymer , physics , organic chemistry
Viscosity data published by the author in 1931 are discussed with reference to their limitations. New experiments on fiber elongation in a redesigned apparatus are described in which one of the glasses previously used is tested. The results show that the viscosity of a newly drawn fiber increases with time of heat treatment according to a definite law which may be explained on the basis of a change in the state of aggregation in the glass. A finite equilibrium viscosity is indicated a t each temperature, this limit being approachable from either side depending on previous heat treatment of the sample. This is taken to indicate an equilibrium average size of aggregate for any temperature, the groups starting to break up again if the temperature is increased after a long treatment. The expression of Sheppard and Houck is used for estimating effective molecular or aggregate weights in equilibrium at various temperatures, an example being 112,000 at about 500°C. The variation of viscosity with time is at least one reason why glasses fail to conform to Adams' and Williamson's annealing equation at low temperatures.

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