A nano-emulsion composition having a small particle size and ultra-low concentration and a preparation method thereof is disclosed. The raw materials of the composition comprise, in terms of percentage by weight, 0.002% to 0.2% of a polymer-containing homogeneous microemulsion, water, and 99.998% to 99.8% of an organic salt solution or inorganic salt solution. The composition is prepared by diluting a polymer-containing homogeneous microemulsion with water or a salt solution. The polymer-containing homogeneous microemulsion is formed by mixing the following raw materials, in terms of percentage by weight: 8% to 40% of a surfactant, 0.5% to 10% of a polymer, 10% to 30% of an alcohol, 3% to 30% of an oil, 0% to 20% of a salt, and balance of water. The composition of the invention is low in concentration, low in cost, narrow in particle size distribution, good in stability, simple in preparation, and convenient for storage and use.

A method for manufacturing an organism adhesion reduction paint includes a first process of gelling a raw material composition that includes polyvinyl alcohol and at least one of a hydroxyl group-containing inorganic compound or an inorganic oxide; a second process of drying and subsequently pulverizing a resulting product in the first process to thereby obtain a composite gel fine powder; and a third process of adding the composite gel fine powder to a main component of a two-component urethane paint and stirring, to thereby prepare a main component of the organism adhesion reduction paint, and also adding a curing agent immediately before use.

A heat energy storage system may have a shape-stabilized composite prepared using an easy impregnation method involving a porous Ca.sup.2+-doped MgCO.sub.3 matrix and PEG as the functional phase. The heat storage capability, microstructures, and interactions with the PEG/CaMgCO.sub.3 composite can be characterized by DSC, SEM imaging, FT-IR spectroscopy, and TGA. Likely because of the synergistic phase change effect of CaMgCO.sub.3 and PEG, the PEG/CaMgCO.sub.3 composites can have high thermal enthalpies, and their enthalpy efficiencies are substantially higher than those of traditional shape stabilized PCMs. The functional material PEG can permeate porous CaMgCO.sub.3 matrices under capillary action. Liquid PEG can be stabilized within the porous matrix, and/or the CaMgCO.sub.3 matrix can improve the thermal stability of the PEG. The high heat energy storage properties and good thermal stability of such organic-inorganic composites offers utility in a range of applications, including thermal energy storage.

A heat energy storage system may have a shape-stabilized composite prepared using an easy impregnation method involving a porous Ca.sup.2+-doped MgCO.sub.3 matrix and PEG as the functional phase. The heat storage capability, microstructures, and interactions with the PEG/CaMgCO.sub.3 composite can be characterized by DSC, SEM imaging, FT-IR spectroscopy, and TGA. Likely because of the synergistic phase change effect of CaMgCO.sub.3 and PEG, the PEG/CaMgCO.sub.3 composites can have high thermal enthalpies, and their enthalpy efficiencies are substantially higher than those of traditional shape stabilized PCMs. The functional material PEG can permeate porous CaMgCO.sub.3 matrices under capillary action. Liquid PEG can be stabilized within the porous matrix, and/or the CaMgCO.sub.3 matrix can improve the thermal stability of the PEG. The high heat energy storage properties and good thermal stability of such organic-inorganic composites offers utility in a range of applications, including thermal energy storage.

A coating composition includes (a) a melamine resin having imino and methylol functional groups that together include 30 mole % or greater of the total functionality of the melamine resin; and (b) at least one polymer reactive with (a) that is obtained from components including polytetrahydrofuran and a carboxylic acid or anhydride thereof. The polytetrahydrofuran includes greater than 20 weight % of the components that form the polymer (b) and the carboxylic acid or anhydride thereof includes greater than 13 weight % of the components that form the polymer (b). The polymer (b) has an acid value ranging from 40 to 60 based on the total resin solids of the polymer (b).

A heat energy storage system may have a shape-stabilized composite prepared using an easy impregnation method involving a porous Ca.sup.2+-doped MgCO.sub.3 matrix and PEG as the functional phase. The heat storage capability, microstructures, and interactions with the PEG/CaMgCO.sub.3 composite can be characterized by DSC, SEM imaging, FT-IR spectroscopy, and TGA. Likely because of the synergistic phase change effect of CaMgCO.sub.3 and PEG, the PEG/CaMgCO.sub.3 composites can have high thermal enthalpies, and their enthalpy efficiencies are substantially higher than those of traditional shape stabilized PCMs. The functional material PEG can permeate porous CaMgCO.sub.3 matrices under capillary action. Liquid PEG can be stabilized within the porous matrix, and/or the CaMgCO.sub.3 matrix can improve the thermal stability of the PEG. The high heat energy storage properties and good thermal stability of such organic-inorganic composites offers utility in a range of applications, including thermal energy storage.

A heat energy storage system may have a shape-stabilized composite prepared using an easy impregnation method involving a porous Ca.sup.2+-doped MgCO.sub.3 matrix and PEG as the functional phase. The heat storage capability, microstructures, and interactions with the PEG/CaMgCO.sub.3 composite can be characterized by DSC, SEM imaging, FT-IR spectroscopy, and TGA. Likely because of the synergistic phase change effect of CaMgCO.sub.3 and PEG, the PEG/CaMgCO.sub.3 composites can have high thermal enthalpies, and their enthalpy efficiencies are substantially higher than those of traditional shape stabilized PCMs. The functional material PEG can permeate porous CaMgCO.sub.3 matrices under capillary action. Liquid PEG can be stabilized within the porous matrix, and/or the CaMgCO.sub.3 matrix can improve the thermal stability of the PEG. The high heat energy storage properties and good thermal stability of such organic-inorganic composites offers utility in a range of applications, including thermal energy storage.

The present invention relates to a process for treating the surface of a polymer article with a UV-stabilizer solution which comprises an effective amount of a UV-absorber compound dissolved in a solvent, and optionally a radical scavenger. The present invention also relates to a process for preparing a UV-stabilized polymer article which comprises a step consisting in contacting the surface layer of a polymer article with the UV stabilizer solution. The present invention also provides UV-stabilized polymer articles, that-is-to-say polymer articles which are resistant to color change upon exposure to UV light.

Provided is a fiber-reinforced thermoplastic resin prepreg which exhibits high interfacial adhesion between reinforcement fibers and a matrix resin, while having excellent interlaminar fracture resistance. The fiber-reinforced thermoplastic resin prepreg of the present invention comprises: a matrix resin comprising a polyarylketone resin and a polyetherimide resin; and a carbon fiber, wherein the polyetherimide resin in the matrix resin comprises a polyetherimide resin having a structural unit represented by Formula (1), an amount of the polyetherimide resin in the matrix resin (100% by mass) is 3% by mass to 25% by mass, and an amount of the polyarylketone resin in the matrix resin (100% by mass) is 75% by mass or more. ##STR00001##

A structured organic film (SOF) is disclosed including a plurality of segments, a plurality of linkers, and a plurality of ionic capping segments, where at least one or more ionic capping segments may include imidazolium. Implementations of the structured organic film (SOF) include where a concentration of ionic capping segments in the SOF is from about 0.1 to about 5.0 molar equivalents of ionic capping segments as compared to a concentration of nonionic segments in the SOF. A thickness of the SOF is from about 100 nm to about 500 ?m. At least one of the plurality of ionic capping segments may include n-hydroxyethyl-1,2,4,5-tetramethylimidazolium (NETMImBr). At least one of the plurality of ionic capping segments may include n-hydroxypropyl-1,2,4,5-tetramethylimidazolium (NPTMImBr). An ion-exchange membrane may include the structured organic film (SOF).