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Compound moisture absorption

Decafluorobiphenyl [434-90-2] C F C F (mol wt, 334.1 mp, 68°C bp, 206°C), can be prepared by I Jllmann coupling of bromo- [344-04-7] chloro- [344-07-0] or iodopentafluorobenzene [827-15-6] with copper. This product shows good thermal stabiHty decafluorobiphenyl was recovered unchanged after 1 h below 575°C (270). Decafluorobiphenyl-based derivatives exhibit greater oxidative stabiHty than similar hydrocarbon compounds (271). Therm ally stable poly(fluorinated aryl ether) oligomers prepared from decafluorobiphenyl and bisphenols show low dielectric constant and moisture absorption which are attractive for electronic appHcations (272). [Pg.328]

The particle size distribution depends on the type of plant (see Table 5). The size of the potato starch granules is considerably higher than the size of com and tapioca starch granules. Also, the moisture absorption of potato starch is much higher than for com and tapioca starch. Thus, processing of tapioca starch in technical processes like compounding is similar to that of com starch [10]. [Pg.107]

Nylon 6/6 is the most widely used, followed by nylon 6, with similar properties except that it absorbs moisture more rapidly and its melting point is 21C (70F) lower. Also, its lower processing temperature and less crystalline structure result in lower mold shrinkage. Nylon 6/6 has the lowest permeability by gasoline and mineral oil of all the nylons. The 6/10 and 6/12 types are used where lower moisture absorption and better dimensional stability are needed. Nylons 11 and 12 have better dimensional stability and electrical properties than the others because they absorb less moisture. These more expensive types also are compounded with plasticizers to increase their flexibility and ductility. With nylon toughening and technology advancements supertough nylons became available. Their notched lzod impact values are over 10 J/m (20 ft-lb/in), and they fail in a ductile manner. [Pg.78]

The last group of non-durable antistats is composed of non-ionic compounds such as ethoxylated fatty esters, alcohols and alkylamines (Fig. 10.3). Mixtures of cationic and non-ionic surfactants demonstrate synergistic antistatic properties. The non-ionic materials provide increased moisture absorption and the cationic products provide the mobile counterions. [Pg.124]

Table III shows the reactivity properties of the molding powder and the physical properties of the cured compound. This table indicates there are virtually no differences in gel times, flow properties, flexural properties, moisture absorption, flame retardancy, and glass transition temperatures between the compound based on stable bromine CEN and the compound based on the standard system of CEN and the epoxy of TBBA. Table III shows the reactivity properties of the molding powder and the physical properties of the cured compound. This table indicates there are virtually no differences in gel times, flow properties, flexural properties, moisture absorption, flame retardancy, and glass transition temperatures between the compound based on stable bromine CEN and the compound based on the standard system of CEN and the epoxy of TBBA.
U0j)(C,04) 3H,0 is prepared by the reported procedure. It is heated at 423 K under vaduum to give anhydrous (UO,)(C,04). To avoid any subsequent moisture absorption, this compound is handled in a nitrogen-filled drybox. [Pg.189]

Noryl phenylene ether-based resins are relatively resistant to burning, and their burn resistance can be increased by judicious compounding. They may be modified with glass and other mineral fillers. Because of low moisture absorption, dimensional stability, and ability to be used over a wide temperature range, Noryl phenylene ether-based resins are especially adaptable to metallizing. However, like most amorphous polymers, they show poor solvent resistance. [Pg.506]

On cooling and storage over P2Os again, the same 378CC peak appears on heating. Moisture absorption by the compound was round to increase the transition temperature. This transition and others can be explained by the reaction scheme... [Pg.399]

Carbon black absorbs all wavelengths of UV light and converts it into heat, while physically blocking UV penetration. For UV-stabilizing effectiveness, various grades of carbon black can be compared in terms of impurity level (affecting taste or odor), particle size, dispersability, and moisture absorption in the compound (which can cause defects in the final part) [4-4]. [Pg.56]

Moisture absorption that needs to be minimized since it may affect the quality of the compound or the stability of hydrolytically sensitive matrices such as nylons or polyesters. [Pg.40]


See other pages where Compound moisture absorption is mentioned: [Pg.442]    [Pg.14]    [Pg.295]    [Pg.28]    [Pg.264]    [Pg.582]    [Pg.354]    [Pg.99]    [Pg.448]    [Pg.405]    [Pg.14]    [Pg.442]    [Pg.264]    [Pg.173]    [Pg.442]    [Pg.30]    [Pg.58]    [Pg.295]    [Pg.62]    [Pg.1031]    [Pg.587]    [Pg.264]    [Pg.6]    [Pg.448]    [Pg.100]    [Pg.204]    [Pg.423]    [Pg.575]    [Pg.120]    [Pg.487]    [Pg.101]    [Pg.31]    [Pg.251]    [Pg.548]    [Pg.406]    [Pg.430]    [Pg.367]    [Pg.601]   


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