A part assembly (100), comprising: an aluminium part (101); a magnesium part (102), the magnesium part (102) coated in a first coating (104); a bond (103), the bond (103) securing the aluminium part (101) to the coated magnesium part (114); wherein the aluminium part (101), the coated magnesium part (114) and the bond (103) are subjected to an electrophoresis coating process to coat the aluminium part (101) in a second coating (105). By subjecting the aluminium part (101), the coated magnesium part (114) and the bond (103) to an electrophoresis coating process to coat the aluminium part (101) in a second coating (105) this may provide a simpler manufacturing process.

A complimentary polymer or dual-polymer electrochromic device and methods of preparing the same are provided.

The present invention is directed towards an electrodepositable coating composition comprising a cationic electrodepositable binder; a phyllosilicate pigment; and a dispersing agent. Also disclosed are methods of making the electrodepositable coating composition, coatings derived therefrom, and substrates coated with the coatings derived from the electrodepositable coating composition.

A process for producing a sensor component for detecting an analyte; a sensor component producible by the process; a process for detecting an analyte; and a device comprising the sensor component. The process comprises electrochemically growing a plurality of conducting polymer molecules from a monomer electrolyte solution to provide a percolation network. The plurality of conducting polymer molecules are grown on the surface of an insulating substrate to connect a first electrode to a second electrode and are capable of displaying a change in an electrical property in response to interaction with an analyte A plurality of conductive nodes may be disposed on a surface of the insulating substrate. A potentiostatic method or a galvanostatic method may be employed to grow the plurality of conducting polymers. Chronoamperometry may be employed to electrochemically grow the plurality of conducting polymers. Cyclic voltammetry is not employed to grow the plurality of conducting polymers.

A substrate coated with a polymer obtained by grafting an aqueous monomer grafting solution comprising a mixture that includes sodium styrene sulphonate (NaSS) and methacrylic acid (MA) or acrylic acid (AA). The mixture has 10 to 90 mol % of sodium styrene sulphonate and 10 to 90 mol % of methacrylic acid or acrylic acid. The substrate is selected from among polyesters, vinyl polymers, polyacrylics and polymethacrylics, PEEK, silicones, natural polymers, natural or artificial celluloses, collagens, glycopolymers, ceramics, metals and metal alloys, and in particular Ti and alloys thereof and NiTi alloys. The aqueous grafting solution has, in addition to the mixture which represents 90 to 99 mol % of the aqueous grafting solution, 1 to 10 mol % of hydroxyethylmethacrylate (HEMA).

Methods of forming and using a polymer dispersion are described herein. The polymer dispersion includes a plurality of polythioaminal microparticles in a fluid medium that does not dissolve the plurality of polythioaminal microparticles. The fluid medium may be aqueous, for example water. The polymer dispersion may be applied to a substrate, and the fluid medium removed, to form an article substantially made of a polymerized polythioaminal mass. The dispersion, and any article made from the dispersion, may include pigments and active ingredients, such as biocides.

Methods of forming and using a polymer dispersion are described herein. The polymer dispersion includes a plurality of polythioaminal microparticles in a fluid medium that does not dissolve the plurality of polythioaminal microparticles. The fluid medium may be aqueous, for example water. The polymer dispersion may be applied to a substrate, and the fluid medium removed, to form an article substantially made of a polymerized polythioaminal mass. The dispersion, and any article made from the dispersion, may include pigments and active ingredients, such as biocides.

Methods of forming and using a polymer dispersion are described herein. The polymer dispersion includes a plurality of polythioaminal microparticles in a fluid medium that does not dissolve the plurality of polythioaminal microparticles. The fluid medium may be aqueous, for example water. The polymer dispersion may be applied to a substrate, and the fluid medium removed, to form an article substantially made of a polymerized polythioaminal mass. The dispersion, and any article made from the dispersion, may include pigments and active ingredients, such as biocides.

A porous structure (1) provided with a pattern that is composed of a conductive polymer, which comprises a porous body (2) and a pattern (3) that is composed of a conductive polymer and arranged on the porous body (2). The porous body (2) is preferably a gel, and a dopant may be added to the pattern (3) that is composed of a conductive polymer. If an agarose gel is used as the gel (2) and a PEDOT electrode (3A) is used as the pattern (3) that is composed of a conductive polymer in the porous structure (1) which is provided with the pattern (3) that is composed of a conductive polymer, the porous structure (1) can be used as an electrode for cell stimulation. The porous structure (1) provided with the pattern (3) that is composed of a conductive polymer can be produced by an electropolymerization method.

Improved formulations of electrophoretic media that can be incorporated into displays, front plane laminates, inverted front plane laminates, or color changing films. The formulations include a non-polar fluid, a plurality of first charged particles, and charge control agents (CCA) including a quaternary amine and an unsaturated polymeric tail comprising monomers of at least 10 carbon atoms in length. The formulations show improved switching speeds, as well as a larger dynamic range at low temperatures (i.e., below about 0 C.), where compared to state-of-the-art electrophoretic media.