Abstract: A boundary layer turbine (BLT) engine has a housing formed by an outer cylinder a first and a second faceplate, a turbine shaft through the faceplates, a stack of alternating disks and spacers with central holes joined to the turbine shaft leaving an outer combustion zone, an air inlet through the first faceplate, an exhaust port through the second faceplate, a fuel port through the outer cylinder, and an ignition device communicating with the combustion zone. The disks and spacers have openings forming separate intake and exhaust channels parallel to the turbine shaft, one channel channeling air from the air inlet port to spaces between disks, and the other channel channeling exhaust from the combustion zone through the exhaust channel to the exhaust port. Fuel is injected into the combustion zone, the air fuel mixture is ignited, and exhaust products impart torque to the turbine shaft by boundary layer friction.

Abstract: A boundary layer turbine (BLT) engine has a housing formed by an outer cylinder a first and a second faceplate, a turbine shaft through the faceplates, a stack of alternating disks and spacers with central holes joined to the turbine shaft leaving an outer combustion zone, an air inlet through the first faceplate, an exhaust port through the second faceplate, a fuel port through the outer cylinder, and an ignition device communicating with the combustion zone. The disks and spacers have openings forming separate intake and exhaust channels parallel to the turbine shaft, one channel channeling air from the air inlet port to spaces between disks, and the other channel channeling exhaust from the combustion zone through the exhaust channel to the exhaust port. Fuel is injected into the combustion zone, the air fuel mixture is ignited, and exhaust products impart torque to the turbine shaft by boundary layer friction.

Abstract: This invention relates to an improved method of preparing an implantable gel or paste for placement between injured bones or placement in bony voids to induce regeneration, and the compositions produced thereby. Specifically, mineral, ceramic, or processed bone particles are coated with a high molecular weight polymer capable of forming a viscous gel when reconstituted with water, saline, autologous blood, sera, or other medically acceptable solution. This high molecular weight polymer coating material may be a natural or synthetic polymeric material, producing a wettable gel upon exposure to water, saline, or another solution. In storage, the composition will be granular and dry but easily wetted. In use, the material is reconstituted to a viscous malleable paste by the simple addition of water or other medically acceptable solution without the need for aggressive mixing. The paste may be delivered by syringe or manually deposited yet will be resistant to lavage or to displacement by gravity induced flow.

Abstract: This invention relates to an improved method of preparing an implantable gel or paste for placement between injured bones or placement in bony voids to induce regeneration, and the compositions produced thereby. Specifically, mineral, ceramic, or processed bone particles are coated with a high molecular weight polymer capable of forming a viscous gel when reconstituted with water, saline, autologous blood, sera, or other medically acceptable solution. This high molecular weight polymer coating material may be a natural or synthetic polymeric material, producing a wettable gel upon exposure to water, saline, or another solution. In storage, the composition will be granular and dry but easily wetted. In use, the material is reconstituted to a viscous malleable paste by the simple addition of water or other medically acceptable solution without the need for aggressive mixing. The paste may be delivered by syringe or manually deposited yet will be resistant to lavage or to displacement by gravity induced flow.

Abstract: A center touch method and apparatus for use in a contact lens station for use with a contact lens mold assembly comprising a first mold half and a second mold half. The center touch apparatus comprises a center touch engaging member having a center touch engaging surface for engaging a central portion of a non-molding surface of one of the mold halves. The center touch method comprising driving one of the mold halves toward the other mold half using the center touch engaging member to contact a central area of the non-molding surface of the one mold half.

Abstract: Ophthalmic lens are made by reacting a lens forming mixture in a mold to form a polymer. The polymer is then demolded from the mold and processed into a completed lens. The molds are made of at least two parts, a first part having a surface for forming the polymer into a portion of the lens and a second part having a surface for forming the polymer into a portion of the lens. The first and second parts of the mold each have different surface energies.

Abstract: A center touch method and apparatus for use in a contact lens station for use with a contact lens mold assembly comprising a first mold half and a second mold half. The center touch apparatus comprises a center touch engaging member having a center touch engaging surface for engaging a central portion of a non-molding surface of one of the mold halves. The center touch method comprising driving one of the mold halves toward the other mold half using the center touch engaging member to contact a central area of the non-molding surface of the one mold half.

Abstract: The present invention is a device that improves visual acuity by reshaping the cornea, by subjectively altering the corneal curvature in the optic zone by increasing the mechanical stiffness of the cornea outside (and/or slightly inside) the optic zone. One or more of the corneal battens are inserted into the cornea, after selectively distorting the natural corneal shape. Once inserted the stiffness of the corneal batten prevents the cornea from returning to its original curvature.

Abstract: An improved method for preventing adhesions during surgery. Tissue surfaces and surgical articles involved in the surgery are coated with a solution of a hydrophilic, polymeric material prior to manipulation of the tissue during surgery. The polymeric material is (1) a substantially water-soluble polymer having at least one C.sub.n F.sub.2n+1 substituent wherein n.gtoreq.4, having a molecular weight of less than about 60,000; (2) a pharmaceutically acceptable salt or complex thereof; or (3) mixtures thereof. The concentration of the aqueous solution of the polymeric material is in the range of from about 0.1% to about 5.0% by weight, the molecular weight and concentration having values such that the aqueous solution is capable of providing wet coatings on the tissue.

Abstract: The present invention relates to a safety lock that is attachable to the trigger of firearms to prevent accidental or unauthorized discharge. The safety lock comprises a pair of opposed plates, one having one or more pins extending normal therefrom, the other having a set of complementary pin-receiving orifices and housing a locking mechanism.

Abstract: A method for producing a biodegradable polymer having a preferentially oriented pore structure and a method for using the polymer to regenerate damaged nerve tissue is disclosed. The preferentially oriented pores are produced by an axial freezing process and serve to promote proper vascularation and regeneration of the damaged nerve. Preferably, the biodegradable polymer comprises uncrosslinked collagen-glycosaminoglycan.

Abstract: A process for preparing a crosslinked collagen-glycosaminoglycan composite material which comprises forming an uncrosslinked composite material from collagen and a glycosaminoglycan and contacting the uncrosslinked composite with a gaseous aldehyde until a crosslinked product having an M.sub.c of from about 800 to about 60,000 is disclosed along with composite materials prepared by this process. Artificial skin produced by this process is more stable toward long-term storage than similar materials prepared using other methods of crosslinking.

Abstract: A monolithic solid state power controller generally comprises a power supply, zero voltage crossing detector, operator interface circuitry, current sensing and trip timing logic (having zero current detection capability), drive circuitry, and a power switch. The current sensing and trip timing logic functions are implemented in a monolithic device which provides flexible mode of operation of the switch, operator command validation, status and mode indication, drive enablement in synchronization with zero voltage crossing of the source voltage, and tripout operation in synchronization with zero current crossing in the load current. Both fast trip (in response to catastrophic overcurrent) and timed trip (in response to overcurrent conditions occurring over a period of time) capabilities are provided.