CARBOXY-TERMINATED BUTADIENE-VINYL FERROCENE COPOLYMERS
First Claim
1. THE CARBOXY-TERMINATED COPOLYMERS OF BUTADIENE AND VNIYL FERROCENE PREPARED BY THE METHOD COMPRISING REACTING VINYL FERROCENE AND THE INITATOR AZOBIS(2-METHYL-4 CARBOXY BUTYRONITRILE) IN AN INERT ORGANIC SOLVENT WITH BUTADIENE AT A REACTION TEMPERATURE AND FOR A REACTION TIME PERIOD SUFFICIENT FOR SAID REACTION TO TAKE PLACE AFTER WHICH SOLVENT REMOVAL IS EFFECTED AND SAID COPOLYMERS ARE DRIED AT A SUITABLE DRYING TEMPERATURE WHILE UNDER REDUCED PRESSURE;
- SAID INERT ORGANIC SOLVENT BEING SELECTED FROM DIOXANE AND TOLUENE;
SAID REACTION TEMPERATURE BEING IN THE RANGE OF ABOUT 60* TO ABOUT 80*C;
SAID REACTION TIME BEING FROM ABOUT 24 HOURS TO ABOUT 120 HOURS;
SAID DRYING IS ACCOMPLISHED AT A SUITABLE TEMPERATURE IN THE RANGE OF ABOUT 70* TO ABOUT 75*C;
SAID REDUCED PRESSURE IS IN THE RANGE OF ABOUT 1 MILLIMETER;
SAID REACTING BUTADIENE AND VINYL FERROCENE IN MOLE RATIOS FROM APPROXIMATELY 100;
1 TO 1;
1 TO FORM SAID COPOLYMERS CHARACTERRIZED BY A MOLECULAR WEIGHT IN THE RANGE FROM ABOUT 1,000 TO ABOUT 10,000, CARBOXY-END GROUP CONTENT OF ABOUT 0.5 WEIGHT PERCENT TO ABOUT 9 WEIGHT PERCENT, AND AN IRON CONTENT OF ABOUT 0.5 WEIGHT PERCENT TO ABOUT 15 WEIGHT PERCENT.
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Accused Products
Abstract
Copolymers of butadiene and vinyl ferrocene (VF) are disclosed along with preparative procedures therefor. The copolymers are produced in an organic solvent when polymerization is initiated by a carboxy-containing azo compound, such as, azobis(2-methyl-4carboxy butyronitrile), thereby forming a copolymer of butadiene and vinyl ferrocene. The copolymers are useful in propellant formulations as a binder where high buring rates are desired.
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Citations
1 Claim
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1. THE CARBOXY-TERMINATED COPOLYMERS OF BUTADIENE AND VNIYL FERROCENE PREPARED BY THE METHOD COMPRISING REACTING VINYL FERROCENE AND THE INITATOR AZOBIS(2-METHYL-4 CARBOXY BUTYRONITRILE) IN AN INERT ORGANIC SOLVENT WITH BUTADIENE AT A REACTION TEMPERATURE AND FOR A REACTION TIME PERIOD SUFFICIENT FOR SAID REACTION TO TAKE PLACE AFTER WHICH SOLVENT REMOVAL IS EFFECTED AND SAID COPOLYMERS ARE DRIED AT A SUITABLE DRYING TEMPERATURE WHILE UNDER REDUCED PRESSURE;
- SAID INERT ORGANIC SOLVENT BEING SELECTED FROM DIOXANE AND TOLUENE;
SAID REACTION TEMPERATURE BEING IN THE RANGE OF ABOUT 60* TO ABOUT 80*C;
SAID REACTION TIME BEING FROM ABOUT 24 HOURS TO ABOUT 120 HOURS;
SAID DRYING IS ACCOMPLISHED AT A SUITABLE TEMPERATURE IN THE RANGE OF ABOUT 70* TO ABOUT 75*C;
SAID REDUCED PRESSURE IS IN THE RANGE OF ABOUT 1 MILLIMETER;
SAID REACTING BUTADIENE AND VINYL FERROCENE IN MOLE RATIOS FROM APPROXIMATELY 100;
1 TO 1;
1 TO FORM SAID COPOLYMERS CHARACTERRIZED BY A MOLECULAR WEIGHT IN THE RANGE FROM ABOUT 1,000 TO ABOUT 10,000, CARBOXY-END GROUP CONTENT OF ABOUT 0.5 WEIGHT PERCENT TO ABOUT 9 WEIGHT PERCENT, AND AN IRON CONTENT OF ABOUT 0.5 WEIGHT PERCENT TO ABOUT 15 WEIGHT PERCENT.
- SAID INERT ORGANIC SOLVENT BEING SELECTED FROM DIOXANE AND TOLUENE;
Specification