57results about How to "Extensive adhesion" patented technology

An image forming apparatus includes a toner image forming section, an intermediate transferring section, a transferring section, a fixing solution applying section, a transporting section, a fixing section, and a recording medium feeding section. In the image forming apparatus, the fixing solution applying section includes a droplet supplying section, a recording medium detecting section, and a control unit, wherein the recording medium is heated before or at the same time when the fixing solution is applied to the recording medium by the fixing solution applying section, and a size of droplets of the fixing solution supplied to the recording medium is controlled based on the type of the recording medium.

In an elongated structure for a movable section, a plurality of operational linear elements such as conductive wires are arranged in parallel in a belt-like sheath member, and an outer region of the sheath member, which is defined by a bend of the sheath member, has a larger rigidity than that of an inner region of the sheath member, which is defined by the bend of the sheath member. When the sheath member 2 have the regions exhibiting the different rigidities, and when an external force is exerted on the elongated structure 1 for the movable section, it is apt to bend toward the side of the sheath member having the small rigidity, and the bent portion is maintained at a given curvature which is determined by the entire rigidity of the sheath member 2. Therefore, the elongated structure 1 for the movable section cannot easily meander while the movable end thereof is moved. Also, while the position of the bent portion is shifted, it is possible to stably carry out the movement of the movable end and the shift of the bent portion. In addition, a protective guide structure is not needed, and not only can an installing space for the elongated structure 1 for the movable section become smaller, but also it is possible to cut down a cost necessary for such a protective guide structure.

There is provided an image forming apparatus involving wet fixing that causes no bleeding and coagulation of toner and eventually no disturbance of toner image as a result of application of a fixing fluid, generates no curling or wrinkles in a recording medium, and can fix toner with large adhesion on a recording medium through which the fixing fluid hardly permeates. An image forming apparatus includes a toner image forming section, an intermediate transfer section, a transfer section, a fixing fluid applying section, a transport section, a fixing section, a recording medium feeding section, and a recording medium detection section. In the image forming apparatus, control of application amount of a fixing fluid to a recording medium is performed by the fixing fluid applying section based on the result obtained by the recording medium detection section for the recording medium such as thickness and material.

A labeling arrangement for labeling beverage bottles. The abstract of the disclosure is submitted herewith as required by 37 C.F.R. §1.72(b). As stated in 37 C.F.R. §1.72(b): A brief abstract of the technical disclosure in the specification must commence on a separate sheet, preferably following the claims, under the heading “Abstract of the Disclosure.” The purpose of the abstract is to enable the Patent and Trademark Office and the public generally to determine quickly from a cursory inspection the nature and gist of the technical disclosure. The abstract shall not be used for interpreting the scope of the claims. Therefore, any statements made relating to the abstract are not intended to limit the claims in any manner and should not be interpreted as limiting the claims in any manner.

An oral pharmabiotic system is disclosed for improving oral, dental, and systemic health by repopulating and reshaping the flora within a patient's oral environment in a manner that overcomes the deficiencies of prior oral probiotic products. By formulating the pharmabiotic system as a strip for adhesive placement within a patients' oral cavity, preferably against the buccal mucosa, alveolar mucosa, oral labial mucosa, or a dental appliance, and configuring the parameters of the strip such that neither disadhesion nor complete dissolution occurs for at least a period of at least three hours during daytime use and at least six hours during nighttime use, the probiotic payload contained within may remain in the oral cavity for a sufficient length of time required for the probiotics to activate, replicate, and displace existing harmful oral pathobiotics.