Formaldehyde-free artificial wood board and preparation method thereof
An artificial wood board and veneer technology, which is applied in the jointing of wooden veneers, veneer presses, manufacturing tools, etc., can solve environmental pollution and other problems, and achieve the effects of reducing pollution, strong implementability, and simple methods
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[0047] Preparation 1
[0048]Preparation of super bonded aqueous polyurethane: An superbly branched aqueous polyurethane in a superbly branched aqueous polyurethane is prepared in the reaction bottle, which is added to 65 ° C, and 5.4 gdMPa is dissolved in 27 ml of the reaction bottle. After the DMF, it was added to the reaction bottle equipped with IPDI, maintained at 65 ° C for 8 h; then fell to -10 ° C, and 4.2 g of DEOA was added dropwise to the reaction system, and after the drop is added, it is kept -10 ° C The reaction was continued for 4 h; then the reaction system temperature was raised to 90 ° C, and 0.027 g as the catalyst was added, and the reaction was continued at 90 ° C for 3 h, resulting in a colorless transparent liquid, 70 ° C to distillation 15 min, and the desired super branched after drying Waterborne polyurethane.
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[0049] Preparation 2
[0050] Preparation of inner cross-linkaged aqueous polyurethane: 12 parts of polycarbonate diol and 12 parts of isocyanate solution were added to the reactor, the control ambient temperature was 80 ° C, reaction 1-2 h; Add 3 parts of acetone, 0.3 In-serial interchange agent, 6 parts of the composite chain extender (wherein the composite chain extender agent comprises 2 parts of dihydroxypropionic acid, 2 parts of dihydroxymethylbutyric acid and 2 parts of trihydroxypropane), 1 part The epoxy delate E51 and 1 part of epoxy dental E-44 were mixed for 2.5 h; after cooling to 30 ° C, then add triethylamine reaction for about 10 min, add 5 parts of deionized water, and allowing the device to heat up the device after 30 min. After 50 ° C, the decompression was distilled, 30 min, thereby producing an intra-crossing aqueous polyurethane emulsion.
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[0051] Preparation Example 3
[0052] Preparation of a composite antibacterial agent: 10 parts of nano silver solution with 5 parts of adhesive fibers were mixed at 90 ° C for 1.5 hours after drying to obtain solid A; in accordance with chloride and urea mixture (in which choline choline and The mass ratio of urea was 2: 1) at a control temperature of 80 ° C for 1 hour, and the solid A was sequentially added at room temperature, and 5 parts of ionized water were sequentially added, 5 parts of butyl titanate were stirred for 1.5 hours to obtain a composite antibacterial agent.
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