Glass thermal stability

Plasma processing technologies ate used for surface treatments and coatings for plastics, elastomers, glasses, metals, ceramics, etc. Such treatments provide better wear characteristics, thermal stability, color, controlled electrical properties, lubricity, abrasion resistance, barrier properties, adhesion promotion, wettability, blood compatibility, and controlled light transmissivity. 

This includes inorganic materials such as glass fibre and mica impregnated or glued together with epoxy, polyesterimide, polyurethane or other resins having superior thermal stability. 

The well-known thermal stability of most minerals and glasses, many of which are themselves polymeric, has led to intensive research into synthetic inorganic and semi-inorganic polymers. These materials can be classified into the following groups ... 

C—S—C) in the main chain. The new polyethers prepared either by new heteroarylene activated or by aromatic activated systems have good melt processability. The thermal stability and glass transition temperature of bisphenol-A based new polymers are shown in Table 10. 

Naqvi [134] has proposed an alternative model to the Frye and Horst mechanism for the degradation and stabilization of PVC. At room temperature, PVC is well below its glass transition temperature (about 81°C). The low thermal stability of the polymer may be due to the presence of undesirable concentrations of like-poles in the more or less frozen matrix with strong dipoles. Such concentrations, randomly distributed in the polymer matrix, may be considered to constitute weak or high energy spots in the polymer, the possible sites of initiation of thermal dehydrochlorination. 

Bowmer and Tonelli [161] have also observed that the magnitude of the glass transition (ACp) increases with the ethylene content of the copolymer, goes through a maximum at about 30 mol%, and then continually decreases until no glass transition is observed at more than 80 mol% of ethylene. This may constitute further evidence in favor of the explanations put forward by Naqvi for the thermal stability behavior of similar copolymers reported by Braun et al. [159]. Initially, with increasing content of nonpolar ethylene units in the co-... 

These techniques help in providing the following information specific heat, enthalpy changes, heat of transformation, crystallinity, melting behavior, evaporation, sublimation, glass transition, thermal decomposition, depolymerization, thermal stability, content analysis, chemical reactions/polymerization linear expansion, coefficient, and Young s modulus, etc. 

Metal Metal, ceramic, carbon, glass fibers Elevated temperature strength Electrical resistance Thermal stability... 

Fluorinated poly(arylene edier)s are of special interest because of their low surface energy, remarkably low water absorption, and low dielectric constants. The bulk—CF3 group also serves to increase the free volume of the polymer, thereby improving various properties of polymers, including gas permeabilities and electrical insulating properties. The 6F group in the polymer backbone enhances polymer solubility (commonly referred to as the fluorine effect ) without forfeiture of die thermal stability. It also increases die glass transition temperature with concomitant decrease of crystallinity. 

In most of the studies discussed above, except for the meta-linked diamines, when the aromatic content (dianhydride and diamine chain extender), of the copolymers were increased above a certain level, the materials became insoluble and infusible 153, i79, lsi) solution to this problem with minimum sacrifice in the thermal properties of the products has been the synthesis of siloxane-amide-imides183). In this approach pyromellitic acid chloride has been utilized instead of PMDA or BTDA and the copolymers were synthesized in two steps. The first step, which involved the formation of (siloxane-amide-amic acid) intermediate was conducted at low temperatures (0-25 °C) in THF/DMAC solution. After purification of this intermediate thin films were cast on stainless steel or glass plates and imidization was obtained in high temperature ovens between 100 and 300 °C following a similar procedure that was discussed for siloxane-imide copolymers. Copolymers obtained showed good solubility in various polar solvents. DSC studies indicated the formation of two-phase morphologies. Thermogravimetric analysis showed that the thermal stability of these siloxane-amide-imide systems were comparable to those of siloxane-imide copolymers 183>. 

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