Hydrocarbon thermal stability

Price L. C. (1997) Minimum thermal stability levels and controlling parameters of methane, as determined by C15+ hydrocarbon thermal stabilities. In Geologic Controls of Deep Natural Gas Resources in the United States (eds. T. S. Dyman, D. D. Rice, and P. A. Westcott). USGS, vol. 2146-K, pp. 139-176. 

Addition of small amount of nanofillers may improve the properties of mbber and thermoplastics. In the polymer industry, polymer-filler nanocomposites are a promising class of material that offers the possibility of developing new hybrid materials with desired set of properties. Properties of mbbers and thermoplastics which have shown substantial improvements due to the incorporation of nanoparticles, are mechanical properties, decreased permeability to gases, water and hydrocarbons, thermal stability and heat distortion temperature, flame retardancy and reduced smoke emissions, chemical resistance, surface appearance, electrical and thermal conductivity, optical clarity in comparison to conventionally filled polymers [107]. 

New copolymers based on a copolymerization of isobutylene and p-methyl-styrene with improved heat resistance have been reported [64]. Once copolymerization was accomplished, the polymer was selectively brominated in the p-methyl position to yield a terpolymer called EXXPO. In contrast to butyl and halobutyl, the new terpolymer has no unsaturation in the backbone and therefore shows enhanced thermal stability and resistance to oxidation. Useful solvent-based adhesives can be formulated using the new terpolymer in combination with block copolymers [65]. The hydrocarbon nature of the new terpolymer results in excellent compatibility with hydrocarbon resins and oils. 

Thermal stabilization of polyolefins has been first demonstrated for low-molecular models-normal structure alkanes [29]. It has been shown that metallic sodium and potassium hydroxide with absorbent birch carbon (ABC) as a carrier are efficient retardants of thermal destruction of n-heptane during a contact time of 12-15 s up to the temperature of 800°C [130]. Olefins and nitrous protoxide, previously reported as inhibitors of the hydrocarbon thermal destruction, are ineffective in this conditions. 

The cationic polymerization of cardanol under acidic conditions has been referred to earlier [170,171], NMR studies [16] indicated a carbonium ion initiated mechanism for oligomerization. PCP was found to be highly reactive with aldehydes, amines, and isocyates. Highly insoluble and infusible thermoset products could be obtained. Hexamine-cured PCP showed much superior thermal stability (Fig. 12) at temperatures above 500°C to that of the unmodified cardanol-formaldehyde resins. However, it was definitely inferior to phenolic resins at all temperatures. The difference in thermal stability between phenolic and PCP resins could be understood from the presence of the libile hydrocarbon segment in PCP. 

Moorite Propellant. A series of rocket proplnts submitted to PicArsn for evaluation in 1949. They consisted of an oxidizer (such as K perchlorate) 70, and a cured rubber hydrocarbon plus accelerators, 30%. Although the examined samples proved to possess desirable props for rocket proplnt use, their thermal stability was poor and their press exponent undesirably high. It was concluded that further work was required on the method of prepn to eliminate these defects... 

Uses. n-Pentane has found use as an anesthetic an expl suppressant when mixed with a halogen-ated hydrocarbon and included in aircraft fuel (Ref 13) a jet engine fuel (Ref 16a) as a base for synthetic rubbers and plastics a parent compd for the formation of nitropentanes and azido nitro pentanes used as expls and propints (Refs 15a, 15b 21a) also, as a parent compd for fluorine-contg resin binders which impart both thermal stability and, in conjunction with metal hydrides, high impulse to solid propints (Ref 15b)... 

A fluid loss additive for hard brine environments has been developed [1685], which consists of hydrocarbon, an anionic surfactant, an alcohol, a sulfonated asphalt, a biopolymer, and optionally an organophilic clay, a copolymer of N-vinyl-2-pyrrolidone and sodium-2-acrylamido-2-methylpropane sulfonate. Methylene-bis-acrylamide can be used as a crosslinker [1398]. Crosslinking imparts thermal stability and resistance to alkaline hydrolysis. 

Fig. 1. Correlation between Thermal Stability and Ground State Strain Eg for hydrocarbons 26 (results from Table 5)...

Engl. 17, 692 (1978). The unusually short central C-C-bond length is in conflict with the low thermal stability of this compound and with the known long C-C-bonds in other crowded hydrocarbons e.g., Destro, R., Pilati, T., Simonetta, M. J. Am. Chem. Soc. 100, 6509(1978)... 

The higher thermal stability of dialkylaluminium hydrides over the corresponding trialkylaluminiums is particularly marked in this case with 2 branched alkyl groups [ ] Used industrially as a powerful reducant, it is supplied as a solution in hydrocarbon solvents. The undiluted material ignites in air unless diluted to below 25%... 

From this point of view attaching of functional groups to common inexpensive fluoropolymers seemed to be a very attractive way to improve the chemical and thermal stability of the final functional polymer materials in comparison with common hydrocarbon functional polymers, while keeping the costs quite reason-... 

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