Exploratory polymer synthesis Summary yearly report, 1 Feb. 1969 - 31 Jan. 1970
Charge transfer processes in synthesis of polymers
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Charge transfer processes in synthesis of polymers
Syntheses and reactions of pyridine type monomers
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Heterocyclic Schiff base type monomer prepared by reaction carbon compounds with amino compounds
Polymerization of prototype monomer xylylidene-2- aminopyridine
Synthesis of Pyrrone polymers from dianhydrides and tetramines in polar solvents
High residue polymer synthesis research at high temperatures
Synthesis of heat resistant azine polymers
Synthesis and evaluation of monomers for synthesis of heat resistant polymers - polymer chemistry
Polymerization of heat resistant aromatic amines - organic chemistry
Heat-resistant azine polymer synthesis by melt and solution method
Synthesis of polymers with high residues at high temperatures
Synthesis of polyimidazopyrrolones, using previous macromolecular synthesis of ladder segments of aromatic-heterocyclic polymers
Model polymer synthesis for use in char forming heat shields
Heterogeneous chemical systems have been studied for the synthesis of isotactic polypropylene in order to establish baseline parameters for the reaction process and to develop sensitive and accurate methods of analysis. These parameters and analytical methods may be used to make a comparison between the polypropylene obtained at one g with that of zero g (gravity). Baseline reaction parameters have been established for the slurry (liquid monomer in heptane/solid catalyst) polymerization of propylene to yield high purity, 98% isotactic polypropylene. Kinetic data for the slurry reaction showed that a sufficient quantity of polymer for complete characterization can be produced in a reaction time of 5 min; this time is compatible with that available on a sounding rocket for a zero-g simulation experiment. The preformed (activated) catalyst was found to be more reproducible in its activity than the in situ formed catalyst.
Ablative polymers synthesis from formaldehyde, phenols and ethers reaction products, discussing char yield, thermally stable fillers incorporation and thermogravimetric analysis
Proposal Objectives: 1. Utilize depolymerization/fractionation techniques to recover highly processable and reactive feedstocks for polymer synthesis from lignin. 2. Synthesize lignin‐derived non‐isocyanate polyurethane, epoxy, and polyamide using non‐ toxic, biobased route designed for chemical recycling. Characterize resulting materials. 3. Design a high‐yielding chemical recycling process for as‐synthesized materials yielding usable building blocks for many generations of polymer synthesis. 4. Optimize chemical recycling of PET waste for the synthesis of lignin‐based polymers. Compare properties to commercial materials. 5. Optimize reaction conditions and recycling steps to facilitate enhanced sustainability of the synthetic steps and final properties of materials. 6. Complete a lifecycle assessment of lignin utilization and chemical recycling to compare their environmental performance to that of materials produced from virgin material. Identify hot spots and benefits using the chemical recycling process.
The synthesis of polymers is discussed. It includes: (1) the synthesis of fluorine-containing crosslinked poly(ether ketones); (2) the synthesis and characterization of poly(imide amides) and their N-methylated analogues; (3) the synthesis of fluorine-containing aromatic polyethers; (4) the synthesis of novel fluorine-containing aromatic polysiloxanes; and (5) the conversion of 6F-containing polythioethers to polysulfones. It is hoped that these polymers will find use as low dielectric materials in electronic applications, function as thermal control coatings, or be suitable elastomeric sealants for extreme service conditions.