Ut-battelle, Inc.

Remaxco Technologies, LLC

Sentech, Inc.

Ut-battle, LLC

Felix Leonard Paulauskas

Soydan Ozcan

Terry L White

Timothy S Bigelow

Daniel M Sherman

Frederic Vautard

Amit Kumar Naskar

Thomas T Meek

Truman Bonds

Orlando Rios

Gerard Michael Ludtka

Paul A Menchhofer

Wyatt Evan Tenhaeff

Gail Mackiewicz Ludtka

Michael Alan McGuire

Karren Leslie More

Claude Clifford Eberle

Mohamed Gabr Abdallah

John Daniel Kennedy Rivard

Kenneth D Yarborough

A functionalized carbon fiber having covalently bound on its surface a partially cured epoxy or amine-containing sizing agent, wherein at least a portion of epoxide or amine groups in the sizing agent are available as uncrosslinked epoxide or amine groups, which corresponds to a curing degree of epoxide or amine groups of no more than about 0.6. Composites comprised of these functionalized carbon fibers embedded in a polymeric matrix are also described. Methods for producing the functionalized carbon fibers and composites thereof are also described.

Solid composites containing polymeric matrix with carbon fibers embedded therein

A method of making a solid composite containing carbon fibers embedded in a polymeric matrix, the method comprising admixing carbon fibers with a polymer precursor resin, and curing the polymer precursor resin to form a cured polymeric matrix that contains said carbon fibers embedded therein, wherein said carbon fibers have covalently bonded on their surfaces a partially cured epoxy-containing or amine-containing sizing agent, wherein at least a portion of epoxide groups or amine groups in the sizing agent are available as uncrosslinked epoxide groups or amine groups, which corresponds to a curing degree of epoxide groups or amine groups of no more than about 0.6.

Method of improving adhesion of carbon fibers with a polymeric matrix

A method of making a carbon fiber having on its surface a partially cured sizing agent, the method comprising covalently binding on the surface of said carbon fiber a sizing agent comprised of an epoxy resin, and partially curing said sizing agent by contact thereof with a curing agent such that at least a portion of epoxide groups remain uncrosslinked on said surface, which corresponds to a curing degree of epoxide groups of no more than about 0.6, and further comprising reacting at least a portion of said epoxide groups with a bifunctional molecule that contains first and second reactive groups, the first reactive group being reactive with and forming a covalent bond with the epoxy group, and the second reactive group being unsaturated and accessible for reaction with a carbon-carbon double bond of an unsaturated resin via a vinyl addition reaction.

A method of processing a carbon fiber tow includes the steps of providing a carbon fiber tow made of a plurality of carbon filaments, depositing a sizing composition at spaced-apart sizing sites along a length of the tow, leaving unsized interstitial regions of the tow, and cross-cutting the tow into a plurality of segments. Each segment includes at least a portion of one of the sizing sites and at least a portion of at least one of the unsized regions of the tow, the unsized region including and end portion of the segment.

Carbon fiber reinforcements for sheet molding composites

A plasma treatment method that includes providing treatment chamber including an intermediate heating volume and an interior treatment volume. The interior treatment volume contains an electrode assembly for generating a plasma and the intermediate heating volume heats the interior treatment volume. A work piece is traversed through the treatment chamber. A process gas is introduced to the interior treatment volume of the treatment chamber. A plasma is formed with the electrode assembly from the process gas, wherein a reactive species of the plasma is accelerated towards the fiber tow by flow vortices produced in the interior treatment volume by the electrode assembly.

Atmospheric pressure plasma processing of polymeric materials utilizing close proximity indirect exposure

A method for producing a carbon fiber, the method comprising: (i) subjecting a continuous carbon fiber precursor having a polymeric matrix in which strength-enhancing particles are incorporated to a stabilization process during which the carbon fiber precursor is heated to within a temperature range ranging from the glass transition temperature to no less than 20&#xb0; C. below the glass transition temperature of the polymeric matrix, wherein the maximum temperature employed in the stabilization process is below 400&#xb0; C., for a processing time within said temperature range of at least 1 hour in the presence of oxygen and in the presence of a magnetic field of at least 1 Tesla, while said carbon fiber precursor is held under an applied axial tension; and (ii) subjecting the stabilized carbon fiber precursor, following step (i), to a carbonization process. The stabilized carbon fiber precursor, resulting carbon fiber, and articles made thereof are also described.

Low temperature stabilization process for production of carbon fiber having structural order

Method for the preparation of carbon fiber from fiber precursor, wherein the fiber precursor is subjected to a magnetic field of at least 3 Tesla during a carbonization process. The carbonization process is generally conducted at a temperature of at least 400&#xb0; C. and less than 2200&#xb0; C., wherein, in particular embodiments, the carbonization process includes a low temperature carbonization step conducted at a temperature of at least or above 400&#xb0; C. or 500&#xb0; C. and less than or up to 1000&#xb0; C., 1100&#xb0; C., or 1200&#xb0; C., followed by a high temperature carbonization step conducted at a temperature of at least or above 1200&#xb0; C. In particular embodiments, particularly in the case of a polyacrylonitrile (PAN) fiber precursor, the resulting carbon fiber may possess a minimum tensile strength of at least 600 ksi, a tensile modulus of at least 30 Msi, and an ultimate elongation of at least 1.5%.

Magneto-carbonization method for production of carbon fiber, and high performance carbon fibers made thereby

A method for continuously processing carbon fiber including establishing a microwave plasma in a selected atmosphere contained in an elongated chamber having a microwave power gradient along its length defined by a lower microwave power at one end and a higher microwave power at the opposite end of the elongated chamber. The elongated chamber having an opening in each of the ends of the chamber that are adapted to allow the passage of the fiber tow while limiting incidental gas flow into or out of said chamber. A continuous fiber tow is introduced into the end of the chamber having the lower microwave power. The fiber tow is withdrawn from the opposite end of the chamber having the higher microwave power. The fiber to is subjected to progressively higher microwave energy as the fiber is being traversed through the elongated chamber.

System to continuously produce carbon fiber via microwave assisted plasma processing

A method for surface treating a carbon-containing material in which carbon-containing material is reacted with decomposing ozone in a reactor (e.g., a hollow tube reactor), wherein a concentration of ozone is maintained throughout the reactor by appropriate selection of at least processing temperature, gas stream flow rate, reactor dimensions, ozone concentration entering the reactor, and position of one or more ozone inlets (ports) in the reactor, wherein the method produces a surface-oxidized carbon or carbon-containing material, preferably having a surface atomic oxygen content of at least 15%. The resulting surface-oxidized carbon material and solid composites made therefrom are also described.

Apparatus and process for the surface treatment of carbon fibers

An apparatus and method for enhancing the surface energy and/or surface chemistry of carbon fibers involves exposing the fibers to direct or indirect contact with atmospheric pressure plasma generated using a background gas containing at least some oxygen or other reactive species. The fiber may be exposed directly to the plasma, provided that the plasma is nonfilamentary, or the fiber may be exposed indirectly through contact with gases exhausting from a plasma discharge maintained in a separate volume. In either case, the process is carried out at or near atmospheric pressure, thereby eliminating the need for vacuum equipment. The process may be further modified by moistening the fibers with selected oxygen-containing liquids before exposure to the plasma.

Growing community of inventors

Knoxville, TN, United States of America

Felix Leonard Paulauskas