Abstract: Methods and apparatus are provided for lining one or more surfaces of concrete structures during fabrication thereof. A structure-lining apparatus comprises a plurality of structure-lining panels and a plurality of concrete-anchoring components. The panels, which may extend in longitudinal and transverse directions, are interconnected to one another in edge-to-edge relationship at their transverse edges to line at least a portion of the interior of the structural form. The concrete-anchoring components extend in an inward/outward direction from the panels. The concrete-anchoring components may: be integrally formed with the panels; connect to the panels via suitably configured connector components; and/or connect edge-adjacent panels to one another. The concrete-anchoring components may comprise concrete-anchoring features which may extend in the longitudinal and transverse directions (e.g. in a plane parallel to the panels) to provide concrete-anchoring surfaces.

Abstract: A process for making a 2-nitro-1-ethanol derivative of formula III: wherein R3 is as described herein is provided. Novel 2-nitro-1-ethanol derivatives provided.

Abstract: A method of fluid forming a container comprising positioning a plastic preform into a mold cavity, wherein the mold cavity defines a first configuration and a first volume. The method further includes injecting a fluid within the plastic preform at a first fluid pressure urging the plastic preform into an expanded shape. The method includes actuating the mold cavity into a second configuration and a second volume, whereby the second volume is smaller than the first volume, thereby resulting in a second fluid pressure within the plastic preform being greater than the first fluid pressure.

Abstract: An hanger apparatus including one or more extension elements with each extension element including a top portion and a bottom portion with the top portion having at least one flexible connector connection with the top portion also in communication with the bottom portion and the bottom portion including apertures for connecting a pool pole-head attachment, with the apparatus additionally including a flexible connector connecting to the at least one flexible connector connection of the top portion.

Abstract: A system for forming a container from a preform, wherein the preform has a finish and a support ring. The system includes a mold having a mold cavity defining an internal surface and adapted to accept the preform, a pressure system having an inlet and an outlet outputting fluid, a blow nozzle receiving the fluid from the pressure system and introducing the fluid at a pressure into the preform thereby expanding the preform toward the internal surface of the mold cavity and creating a resultant container. The system further includes a first seal engagement selectively engageable between the blow nozzle and the finish of the preform and a second seal engagement selectively engageable between the blow nozzle and an adjacent feature.

Abstract: A mold device for forming a plastic container from a preform. The preform includes at least one exterior feature formed thereon. The mold device comprises a mold defining a mold cavity, and a central exterior rod being movable within the mold cavity. The central exterior rod includes a locating feature formed therewith that is engagable with the at least one exterior feature of the preform for maintaining a central orientation of the preform within the mold cavity during forming.

Abstract: A stay-in-place form-work for casting a concrete structure comprises a plurality of elongate panels interconnectable in edge-to-edge relationship via complementary connector components on their longitudinal edges to define at least a portion of a perimeter of the form-work. The panels include a first panel having a first connector component incorporating a receptacle, and a second panel having a second connector component incorporating a protrusion. The first and second panels are connectable to one another in edge-to-edge relationship by: effecting a loose-fit connection by extending the protrusion of the second connector component into the receptacle of the first connector component; loosely seating a clip onto the first and second connector components; and pushing the clip against the first and second connector components to reach a locked configuration wherein restorative deformation forces associated with the clip act to retain the first and second connector components in the locked configuration.

Abstract: A mold for forming a plastic container having an integrally formed standing ring. The mold includes a first mold portion and a second mold portion. The second mold portion is movable relative to the first mold portion. The first mold portion and the second mold portion together define at least in part a mold cavity for molding a plastic container. The first mold portion and the second mold portion together define a standing ring slot for forming a standing ring on a base portion of the plastic container. The standing ring slot is defined at an interface between the first mold portion and the second mold portion.

Abstract: Feature analysis on consecutive tissue sections (FACTS) includes obtaining a plurality of consecutive tissue sections from a tissue sample, staining the sections with at least one biomarker, obtaining a digital image thereof, and identifying one or more regions of interest within a middle of the consecutive tissue sections. The digital images of the consecutive tissue sections are registered for alignment and the one or more regions of interest are transferred from the image of the middle section to the images of the adjacent sections. Each image of the consecutive tissue sections is then analyzed and scored as appropriate. Using FACTS methods, pathologist time for annotation is reduced to a single slide. Optionally, multiple middle sections may be annotated for regions of interest and transferred accordingly.

Abstract: ClotGel is a single-component hemostatic agent designed for use as an adjunct or primary treatment in moderate intraoperative hemorrhage and in trauma. It can be applied topically to the wound either on the skin in a laparatomy or as non-invasive manner in surgical procedures. Its crosslinking technology generates an adhesive stable fibrin clot using a single component (fibrin II) required for hemostasis. The agent is a mixture of lyophilized polymerized fibrin II and fibrin II monomer which is polymerized and stabilized when in contact with the blood. The attachment properties of the gel, as well as the rapid formation of a fibrin clot, ensures that a strong stable fibrin clot is formed within 1 minute of application.

Abstract: An apparatus for a stay-in-place form assembly comprises a plurality of elongated panels connectable to one another in edge-to-edge relationship. The plurality of panels comprise first and second panels connectable to one another at a connection between a generally male connector component of the first panel and a generally female connector component of the second panel. The generally female connector component comprises a female engagement portion which defines a principal receptacle and the generally male connector component comprises a male engagement portion which is received in the principal receptacle to form the connection. The generally female connector component comprises a first abutment portion and the generally male connector component comprises a second abutment portion which abuts against the first abutment portion to form the connection. The first and second abutment portions are located outside of the principal receptacle.

Abstract: ClotBlock is a lyophilized fibrin hemostatic designed for use an adjunct or primary treatment in moderate to severe hemorrhage. It can be applied directly to the wound in a laparotomy procedure or as non-invasive sealant. Its crosslinking technology generates a strong and safe adhesive fibrin sealant required for high volume hemostasis. The attachment properties of the cake as well as the rapid formation of and stability of the fibrin clot ensures that a strong stable fibrin clot is formed within 1 to 5 minutes depending on the grade of the wound. The agent is safe, biocompatible, biodegradable and can be stored at room temperature for one year.

Abstract: A mold device for injecting a fluid into a container where the mold device comprises a first mold portion having a first mating surface and a second mold portion having a second mating surface. The second mating surface is shaped complementary to the first mating surface. A mold cavity is disposed within the first mold portion and the second mold portion. The mold device further comprises an interlocking mating surface system disposed between or made a part of the first mold portion and second mold portion to define a fluid seal therebetween and align the first mold portion to the second mold portion in at least a first direction.

Abstract: A method for marking a petroleum hydrocarbon or a liquid biologically derived fuel by adding at least one compound having formula (I), wherein R1 and R2 independently represent hydrogen or C1-C4 alkyl groups, and G represents hydrogen or at least one substituent selected from the group consisting of C1-C18 alkyl and C1-C18 alkoxy.

Abstract: ClotFoam is a sealant and hemostatic agent for use in cases of non-compressible hemorrhage for moderate to severe bleeding. It can be applied in the operating room through laparoscopic ports, or directly over lacerated tissue in laparotomy procedures or outside the operating room through a mixing needle and/or a spray injection method following intracavitary severe trauma or surgery. Its crosslinking technology generates an adhesive scaffold that carries a fibrin sealant required for hemostasis. Clotfoam produces a foam that spreads throughout a body cavity reaching the lacerated tissue to seal tissue and promote the coagulation cascade. The composition is biocompatible and non-inflammatory. The invention uses fibrin monomer polymerized by a change of pH as active sealing component. The viscoelastic properties of the foam as well as the rapid formation of a fibrin clot ensure that the sealant remains at the site of application without being washed away by blood.

Abstract: A compound having formula (I), wherein G1 represents a C4-C22 alkyl or alkenyl group, a C8-C20 aralkyl group or formula (II) wherein G3 is a difunctional C2-C18 alkyl or alkenyl group, a difunctional C6-C20 aryl group or G3 is absent; provided that G1 is not 2-butyl, n-hexyl, n-octyl, n-dodecyl, n-hexadecyl or 2-phenylethyl.

Abstract: A method for marking a petroleum hydrocarbon or liquid biologically derived fuel by adding to the petroleum hydrocarbon or biologically derived fuel at least one compound having formula (I), wherein G1 represents an organic functional group having from four to forty carbon atoms.

Abstract: Encapsulated organic electronic devices including organic light emitting diodes are made using an adhesive component as a mask while the device is being constructed. An adhesive-coated liner can be applied to the device substrate and openings created therein by removing portions of the liner and adhesive, or a patterned adhesive layer having openings therein can be formed on the device substrate, followed by deposition of the device layers and application of a sealing layer.

Abstract: Methods and apparatus are provided for repairing existing structures. A portion of the existing structure is covered with the repair structure. One or more standoffs are coupled to the existing structure to project outwardly away from a surface of the existing structure. One or more cladding panels are coupled to the standoffs by forcing the one or more panels in a direction normal to the surface of the existing structure and into engagement with a standoff connector component of the standoff at a location spaced apart from the existing structure. Curable construction material and/or insulation may be introduced into the space between the cladding panels and the existing structure to provide a repair structure.

Abstract: An ultrasonic transducer device is disclosed. The device includes a body and an ultrasonic transducer mounted onto the body. The ultrasonic transducer comprises a shoulder and an O-ring placed on the shoulder. The O-ring substantially covers the interface between the ultrasonic transducer and the body.