Abstract: A method for producing thing glass strips is provided that avoids camber defects. The method includes using a glass strip forming device that has a drawing device; drawing, using the drawing device, the thin glass strip away from the glass strip forming device; measuring, using a measuring device, variables that are dependent on a differing length of edges of the thin glass strip at at least two measurement locations spaced apart transversely to a longitudinal extension of the thin glass strip; determining a difference or a quotient of the variables. The difference or the quotient is used to determine a control variable by which the glass strip forming device is controlled so as to counteract a difference in velocities of the thin glass strip between the two opposite edges.

Abstract: A system and a method include a display configured to display video and/or still images, and an image source that is in communication with the display and configured to allow content of the image source to be displayed on the display. Further, the system and method include a physiological information gatherer configured to obtain a current physiological information of a patient when the patient is positioned to see the video and/or still image on the display. A processor is configured to receive the current physiological information from the physiological information gatherer, and the processor, being in communication with the image source, is further configured to transmit to the display the current physiological information and a target breathing rate.

Abstract: A glass roll, as well as a device and a method for manufacturing the glass roll are provided. The glass roll includes a glass ribbon having a thickness, a length in an x-direction, and a width in a y-direction. The glass ribbon has at least one defect site at a position, as well as at least one error mark disposed on the glass ribbon, and is wound up into a glass roll.

Abstract: The invention relates to a method and a system for reducing anxiety of patients before and during e.g. MR scanning examinations. The method is based on displaying images on walls (106,107) of the scanner room (100) so that when the patient enters the scanner room, then an image is displayed on a wall visible to the patient, e.g. a wall adjacent to the entry door (103). When the patient is laying on the table (102) of the scanner (101) the projection of images is switched to another wall by reflecting the projected images using e.g. a mirror which is moved into the light rays emitted by an image projector.

Abstract: A method and apparatus for scoring thin glass for the purpose of score and break separation as well as an accordingly prepared scored thin glass are provided. The scoring tool is pressed onto the thin glass and drawn along the scoring line with an adjusted scoring contact pressure force as a vertical scoring force component. This permits to production of prescored ultrathin glass of Knoop hardness from 350 to 650 with a score depth from 1/20 to ? of the material thickness.

Abstract: The invention provide a method for making silicone hydrogel based on the Lightstream Technology from a monomer mixture with a curing time of less than about 100 seconds. The present invention is also related to silicone hydrogel contact lenses made according to methods of the invention.

Abstract: A decompression arrangement includes first and second cabin lining elements each with an edge region, the edge region of the second being arranged at a smaller distance from an aircraft outer skin than the edge region of the first, an air discharge opening arranged between the first edge region and second edge region and which is adapted to discharge air from an inner region of the cabin delimited by the cabin lining elements into a region of the aircraft lying between the cabin lining elements and the aircraft outer skin, and a decompression element integrated in the second cabin lining element having a flap pivotable about an axis from a closed position, in which it closes a pressure equalizing opening formed in the decompression element, into a first open position, in which it opens the pressure equalizing opening if a first predetermined differential pressure acts on the decompression element.

Abstract: The present invention is directed to an implant device, in particular an implant device placed between bony, cartilaginous or soft tissues or between prosthetic surfaces to restore or create a gap. More particular the present invention is directed to an implant device made from polymeric material and having a stiffness gradient as well as a limited dimensional deformation, wherein the implant device has a stiffness gradient and a limited dimensional deformation and preferably is at least partially anisotropic.

Abstract: A glass roll includes at least one glass film and one intermediate material one on top of the other in at least two layers onto a winding core. The glass film layers are held in place by the intermediate material layers. The glass roll is produced with a method including provision of a glass film, a winding core and a compressible intermediate material. At least one inside layer of the intermediate material is wound onto the winding core. The glass film and the intermediate material are wound onto the winding core in such a manner that the glass film is wound onto the winding core in alternating layers with the intermediate material. The intermediate material and/or the glass film is wound at a tensile stress acting in a longitudinal direction which causes a compression of the intermediate material and holds the glass film end in place on the glass roll.

Abstract: A glass film has a first and a second surface which are both defined by like edges, wherein the surface of at least two edges which are located opposite one another have an average surface roughness of an maximum of 2 nanometers.

Abstract: A glass film has a thickness of less than 1.2 mm, and a first and a second surface, both surfaces being defined by edges having an edge surface. The respective edge surfaces are provided with a microstructure surface, including micro-cracks and fissures which are laterally defined by flanks. At least two edges located opposite one another include a low viscosity adhesive having a viscosity of less than 600 mPas at 23° C., on their microstructure surfaces in such a way that the respective flanks of the micro-cracks and fissures are bonded together using an adhesive so that the probability of failure of the glass film having a length of 1000 m and a thickness in the range of 5 ?m to 350 ?m, and a diameter of a wound glass film roll in the range of 50 mm to 1000 mm is less than 1%.

Abstract: A method for separating a thin glass sheet, such as a glass film along a predefined cutting line provides the cutting line immediately has a temperature of greater than 250 K below the transformation point Tg of the glass of the thin sheet of glass, including the input of energy along the cutting line using a laser beam which acts such that a separation of the thin glass sheet occurs.

Abstract: The present invention relates to a system (10) comprising a display unit (12) configured for displaying video and/or still images, an image source (14) in communication with the display unit (12) so as to allow content of the image source (14) to be displayed on the display unit (12), a physiological information gathering unit (16) configured to obtain current physiological information of a patient when the patient is positioned to see the video and/or still image on the display unit (12), a processor (18) for receiving current physiological information from the physiological information gathering unit (16), the processor (18) being in communication with the image source (14), the processor (18) being configured to transmit to the display unit (12) a combination of the current physiological information and a target breathing rate. Further the present invention relates to a respective method (36) for using the system (10).

Abstract: A method for making a silicone hydrogel contact lens is provided. In one embodiment, a prepolymer mixture is polymerized in a lens mold in an atmosphere having less than about 10000 ppm oxygen to form a silicone hydrogel contact lens suitable for extended wear as characterized by producing less than 10% corneal swelling after a period of continuous wear of 7 days including normal sleep periods. In one embodiment, the prepolymer mixture comprises at least one oxyperm material containing hydrophilic groups, wherein the at least one oxyperm material is a siloxane-containing macromer or monomer, at least one ionperm material, and a cross-linking agent. In certain embodiments, the polymerization of the prepolymer mixture may be carried out in an atmosphere having less than about 1000 ppm oxygen.

Abstract: There is described a composition for forming an contact lens, in particular for forming a silicone hydrogel contact lens, comprising at least one first vinylic monomer or macromer having one first ethylenically unsaturated group and at least one second vinylic monomer or macromer having one second ethylenically unsaturated group, wherein the first and second ethylenically unsaturated groups are different from each other and wherein the composition further comprises a crosslinker with at least two ethylenically unsaturated (polymerizable) groups with a selected kinetic copolymerization parameter r1 of less than 1.0 relative to one of the first and second ethylenically unsaturated (polymerizable) groups as defined above.

Abstract: A method for making a silicone hydrogel contact lens is provided. In one embodiment, a prepolymer mixture is polymerized in a lens mold in an atmosphere having less than about 10000 ppm oxygen to form a silicone hydrogel contact lens suitable for extended wear as characterized by producing less than 10% corneal swelling after a period of continuous wear of 7 days including normal sleep periods. In one embodiment, the prepolymer mixture comprises at least one oxyperm material containing hydrophilic groups, wherein the at least one oxyperm material is a siloxane-containing macromer or monomer, at least one ionoperm material, and a cross-linking agent. In certain embodiments, the polymerization of the prepolymer mixture may be carried out in an atmosphere having less than about 1000 ppm oxygen.

Abstract: The invention relates to a method and a system for reducing anxiety of patients before and during e.g. MR scanning examinations. The method is based on displaying images on walls (106,107) of the scanner room (100) so that when the patient enters the scanner room, then an image is displayed on a wall visible to the patient, e.g. a wall adjacent to the entry door (103). When the patient is laying on the table (102) of the scanner (101) the projection of images is switched to another wall by reflecting the projected images using e.g. a mirror which is moved into the light rays emitted by an image projector.

Abstract: A patient monitoring system comprises a probe module (10) to acquire data of a patient to be monitored. An evaluation module (20) to determines a patient's state of anxiety on the basis of the acquired data. An indicator module (30) to feedback the determined state of anxiety to attending staff. Thus, the staff is enabled on the basis of the feedback from the patient monitoring system to re-assure patients where that is needed and beneficiary.

Abstract: A window funnel for an aircraft is provided, which has a ring made of an elastic material, which is arranged by means of an adhesive layer on an outer side of the window funnel, the ring having a hollow profile. The ring serves as a sight screen, light screen and dust screen for the rear side of the window funnel.

Abstract: An ophthalmic lens suited for extended-wear periods of at least one day on the eye without a clinically significant amount of corneal swelling and without substantial wearer discomfort. In one embodiment, an ophthalmic lens is a copolymerization product of at least one oxyperm, at least one ionoperm, and a crosslinker. In one embodiment, a lens has a tensile modulus of less than about 3.0 MPa, yet in another embodiment, the tensile modulus is between about 0.5 to about 1.5 MPa.