Amorphous viscosity

The highly crystalline cotton cellulose (COC) sorbs some more vapor of the alcohol than highly amorphous viscose fibers (VF). Thus, the sorption of the propanol vapor is not depended on degrees of amorphicity or crystallinity. The probably sorption mechanism in the propanol-cellulose system is an adsorption on the surface of cellulose pores. 

Sihcate solutions of equivalent composition may exhibit different physical properties and chemical reactivities because of differences in the distributions of polymer sihcate species. This effect is keenly observed in commercial alkah sihcate solutions with compositions that he in the metastable region near the solubihty limit of amorphous sihca. Experimental studies have shown that the precipitation boundaries of sodium sihcate solutions expand as a function of time, depending on the concentration of metal salts (29,58). Apparently, the high viscosity of concentrated alkah sihcate solutions contributes to the slow approach to equihbrium. 

Solution Deposition of Thin Films. Chemical methods of preparation may also be used for the fabrication of ceramic thin films (qv). MetaHo-organic precursors, notably metal alkoxides (see Alkoxides, metal) and metal carboxylates, are most frequently used for film preparation by sol-gel or metallo-organic decomposition (MOD) solution deposition processes (see Sol-GEL technology). These methods involve dissolution of the precursors in a mutual solvent control of solution characteristics such as viscosity and concentration, film deposition by spin-casting or dip-coating, and heat treatment to remove volatile organic species and induce crystaHhation of the as-deposited amorphous film into the desired stmcture. 

Resin Low MW (<5000) Tg usually > RT Amorphous Lower viscosity Improve wet out Adjust Tg of system... 

In most adhesives, tackifier is the ingredient present in the highest proportion. Tackifying resins are primarily used to reduce adhesive viscosity and adjust the 7g of the adhesive s amorphous matrix phase. Through their effects on the other ingredients and the overall system they can also dramatically affect wet out, hot tack, open time, set speed, and heat resistance. 

All of the eommereial alkyl eyanoaerylate monomers are low-viseosity liquids, and for some applications this can be an advantage. However, there are instances where a viseous liquid or a gel adhesive would be preferred, sueh as for application to a vertical surface or on porous substrates. A variety of viscosity control agents, depending upon the desired properties, have been added to increase the viscosity of instant adhesives [21]. The materials, which have been utilized, include polymethyl methacrylate, hydrophobic silica, hydrophobic alumina, treated quartz, polyethyl cyanoacrylate, cellulose esters, polycarbonates, and carbon black. For example, the addition of 5-10% of amorphous, non-crystalline, fumed silica to ethyl cyanoacrylate changes the monomer viscosity from a 2-cps liquid to a gelled material [22]. Because of the sensitivity of cyanoacrylate esters to basic materials, some additives require treatment with an acid to prevent premature gelation of the product. 

Miscibility or compatibility provided by the compatibilizer or TLCP itself can affect the dimensional stability of in situ composites. The feature of ultra-high modulus and low viscosity melt of a nematic liquid crystalline polymer is suitable to induce greater dimensional stability in the composites. For drawn amorphous polymers, if the formed articles are exposed to sufficiently high temperatures, the extended chains are retracted by the entropic driving force of the stretched backbone, similar to the contraction of the stretched rubber network [61,62]. The presence of filler in the extruded articles significantly reduces the total extent of recoil. This can be attributed to the orientation of the fibers in the direction of drawing, which may act as a constraint for a certain amount of polymeric material surrounding them. 

There is greater similarity in the behavior of stretched melts and solid samples prepared by, e.g. pressure molding, probably, for the reason of parallelism in structure formation and destruction caused by deformation in melts and the amorphous regions of solid matrices. It is also possible to use identical equations for longitudinal viscosity and strength which present them as functions of the filler concentration [34]. 

The load or stress has another effect on the creep behavior of most plastics. The volume of isotropic or amorphous plastic increases as it is stretched unless it has a Poisson ratio of 0.50. At least part of this increase in volume manifests itself as an increase in free volume and a simultaneous decrease in viscosity. This decrease in turn shifts the retardation times to being shorter. 

Tammaun has advanced the view that amorphous solids are really liquids which have been cooled far below their freezing-points, and have thereby acquired great viscosity, but have not crystallised. They are supercooled liquids. This hypothesis is supported by the following evidence ... 

Continuous transition of state is possible only between isotropic states it may thus occur between amorphous glass (i.e., supercooled liquid of great viscosity) and liquid ( sealing-wax type of fusion ), or between liquid and vapour, but probably never between anisotropic forms, or between these and isotropic states. This conclusion, derived from purely thermodynamic considerations, is also supported by molecular theory. 

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