Modification of Oligomers and Reinforced Polymeric Composites by Carbon Nanotubes and Ultrasonic

An abridged version of the book chapter is presented in the archive. Full version on the publisher's site: https://link.springer.com/chapter/10.1007/978-3-030-26672-1_3Розглядається широке коло питань щодо розроблених напрямів модифікації епоксидних олігомерів і армованих полімерних композитів на їх основі вуглецевими нанотрубками і ультразвуком. Аналізується перспективність створення гібридних полімерних композитів функціонального призначення.This chapter analyzes the physical (in the form of ultrasound) and chemical modification of liquid polymer media and reinforced polymeric composites. The main emphasis is made on the analysis of ultrasonic cavitation processing as the most effective one for solving one of the main technological problems in the production of nanomodified polymer composites

Insights on self-assembly of carbon in the processes of thermal transformations under high pressures

Peculiarities of the processes of self-assembly of carbon under pressure up to 8 GPa and temperatures up to 1600°C in pure carbon, hydrocarbon, fluorocarbon, organometallic systems and binary mixtures of all-carbon, hydrocarbon, and fluorocarbon compounds have been revealed in the course of studies of pressure and temperature-induced transformations of different carbon-containing systems. It was shown that the character of the processes of self-assembly of carbon in different systems is controlled in the first place by the mobility of carbon atoms. The low diffusion mobility of carbon atoms in a condensed state at temperatures below 2000° C leads to the fact that in pure carbon systems studied on the examples of fullerite C60 and closed polyhedral carbon nanoparticles, carbon self-organization can occur only due to processes associated with small movements of carbon atoms that ensure the formation of intermolecular bonds in cases of polymerization of C60 or the restructuring of the internal structure of a polyhedral particle, strictly limited to the confines of a single nanoparticle. In the hydrocarbon and fluorocarbon systems, the character of transformation changes drastically due to formation of volatile low-molecular hydrocarbon and fluorocarbon fractions, which ensure a high gas-phase or fluid mobility to carbon atoms. Studies of pressure and temperature-induced transformations of different hydrocarbon, fluorocarbon compounds and their homogeneous binary mixtures revealed a clear synergistic effect of fluorine and hydrogen on processes of carbonization, graphitization, and formation of diamond in these systems in relation to industrially significant reduction of p,T parameters for formation of graphite, diamond and increase in the content of nanosize diamond fractions in the products of transformations of binary mixtures in comparison with pure hydrocarbon and fluorocarbon compounds. Discovery of this synergistic effect opens new opportunities for synthesis of high-purity and doped ultranano-, nano-, submicro-, and micronsized diamonds with the specific properties for different applications in quantum physics and biomedicine. Studies of particularities of self-assembly of carbon in processes of thermal transformations of ferrocene at high pressures demonstrated the possibility of preparation of iron carbide nanoparticles encapsulated into carbon shells, Fe7C3@C and Fe3C@C, considered as perspective magneto-controlled platforms for different biomedical nanocomplexes

Synergistic Influence of Fluorine and Hydrogen on Processes of Thermal Transformations of Carbon-Containing Systems under High Pressures

International audience[No abstract

Methods for preparing carbon nanotube/polymer composites using free radical precursors

In some embodiments, the present invention is directed to methods of fully integrating CNTs and the surrounding polymer matrix in CNT/polymer composites. In some such embodiments, such integration comprises interfacial covalent bonding between the CNTs and the polymer matrix. In some such embodiments, such interfacial covalent bonding is provided by a free radical reaction initiated during processing. In some such embodiments, such free radical initiation can be provided by benzoyl peroxide. In some or other embodiments, the present invention is directed to CNT/polymer composite systems, wherein the CNTs within such systems are covalently integrated with the polymer. In some or other embodiments, the present invention is directed to articles of manufacture made from such CNT/polymer composite systems

Fiber-reinforced polymer composites containing functionalized carbon nanotubes

The present invention is directed to methods of integrating carbon nanotubes into epoxy polymer composites via chemical functionalization of carbon nanotubes, and to the carbon nanotube-epoxy polymer composites produced by such methods. Integration is enhanced through improved dispersion and/or covalent bonding with the epoxy matrix during the curing process. In general, such methods involve the attachment of chemical moieties (i.e., functional groups) to the sidewall and/or end-cap of carbon nanotubes such that the chemical moieties react with either the epoxy precursor(s) or the curing agent(s) (or both) during the curing process. Additionally, in some embodiments, these or additional chemical moieties can function to facilitate dispersion of the carbon nanotubes by decreasing the van der Waals attractive forces between the nanotubes