Fabric chemical plating method using HBP-NH2/ Ag+ coordination compound as activate fluid
A technology of HBP-NH2 and coordination compounds, which is applied in the fields of chemical engineering and textile functional finishing, can solve the problems of complex activation process, scarce sources, high price, etc., achieve high conductivity, uniform distribution of catalyst silver, and reduce preparation costs Effect
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Embodiment 1
[0038] (1) hyperbranched polyamide-amine (HBP-NH 2 )Synthesis
[0039] Add a mixed solution of 103.17g diethylenetriamine and 45mL methanol to a 500mL three-necked round-bottomed flask, and place it in an ice-water bath. The mixed solution was added into the diethylenetriamine solution, and reacted for 12 hours to obtain a diethylenetriamine-methyl acrylate polymeric precursor.
[0040] The obtained polymeric precursor was transferred to the eggplant-shaped bottle of the rotary evaporator, and the reaction system was evacuated by a circulating water multi-purpose vacuum pump. At the same time, the temperature of the system was raised to 60 ° C in the oil bath during the high-speed rotation. React at 60°C for 1 hour, extract the methanol in the solvent; then raise the reaction temperature to 140°C, and react for 2 hours to obtain HBP-NH 2 .
[0041] (2)HBP-NH 2 / Ag + Preparation of Activation Finishing Solution
[0042] First prepare HBP-NH with a concentration of 10g / L ...
Embodiment 2
[0049] (1) hyperbranched polyamide-amine (HBP-NH 2 )Synthesis
[0050] Add the mixed solution of 60.1g ethylenediamine and 45mL methanol to a 500mL three-neck round bottom flask, and place it in an ice-water bath. The mixed solution was added into the ethylenediamine solution, and reacted for 12 hours to obtain an ethylenediamine-methyl acrylate polymer precursor.
[0051] The obtained polymeric precursor was transferred to the eggplant-shaped bottle of the rotary evaporator, and the reaction system was evacuated by a circulating water multi-purpose vacuum pump. At the same time, the temperature of the system was raised to 60 ° C in the oil bath during the high-speed rotation. React at 60°C for 1 hour, extract the methanol in the solvent; then raise the reaction temperature to 140°C, and react for 2 hours to obtain HBP-NH 2 .
[0052] (2)HBP-NH 2 / Ag + Preparation of Activation Finishing Solution
[0053] With the step (2) of embodiment 1.
[0054] (3) Activation treatm...
Embodiment 3
[0059] (1) HBP-NH 2 Synthesis
[0060] The synthesis process is the same as the step (1) of Example 1.
[0061] (2)HBP-NH 2 / Ag + Preparation of Activation Finishing Solution
[0062] Prepare 10g / L of HBP-NH 2 solution and 10g / L silver nitrate solution, slowly add 10mL10g / L silver nitrate to 20mL10g / L HBP-NH 2 solution, and diluted to 100mL, after the mixed solution was shaken, it was left to stand in a water bath at 30°C for 30 hours to obtain HBP-NH 2 / Ag + Activation finishing solution, wherein the content of silver nitrate is 1g / L.
[0063] (3) Activation treatment of fabric
[0064] With the step (3) of embodiment 1.
[0065] (4) Electroless plating
[0066] The method of electroless copper plating is the same as step (4) of Example 1. The average surface resistance of the prepared conductive polyester fabric is 8mΩ / sq, and the electromagnetic shielding efficiency is about 85dB.
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