A kind of inorganic composite guanidine salt polymer anti-harmful microorganism material and preparation method thereof
A technology of guanidine salt polymer and compound guanidine salt, applied in the field of materials, can solve the problems of increasing enterprise cost, difficult loss of guanidine salt polymer, loss of antibacterial properties, etc., to achieve efficient antibacterial properties, no bacterial resistance, wide spectrum antibacterial effect
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[0033] The present invention also provides a preparation method of an inorganic composite guanidinium salt polymer anti-harmful microorganism material, comprising the following steps:
[0034]S1: Mix the inorganic powder functionalized with epoxy group, guanidinium salt polymer, polyether polyol and methyl silicone oil evenly. Under the protection of inert gas, raise the temperature and stir to melt the polymer material and mix with epoxy group Mix the group-functionalized inorganic powder evenly, and react at 100-200°C for 30 minutes to 8 hours, and chemical grafting reaction modification occurs on the surface of the epoxy-functionalized inorganic powder (the surface is chemically bonded into a band resistant guanidinium salt polymers with functional groups harmful to microorganisms);
[0035] S2: After the step S1 reaction finishes, the product in molten state is cooled to room temperature, and then the cooled solid product is pulverized;
[0036] S3: The product of step S2...
Embodiment 1
[0042] Add 100g of fumed silica that has been pre-dried at 120°C for 5 hours to 3000ml of anhydrous ethanol aqueous solution (mass ratio of absolute ethanol:distilled water is 3:1), and adjust the pH value to 4~ with hydrochloric acid. 5. Start stirring and assist the ultrasonic environment to make it uniformly dispersed for 30 minutes, then slowly drop 20g of γ-glycidyl etheroxypropyl trimethoxysilane (CAS No.: 2530-83-8), and then heat up to 70°C. After stirring at constant temperature for 10 hours, suction filter the suspension of white carbon black, wash it with absolute ethanol for 3 times, dry and grind to obtain epoxy group functionalized white carbon black and store it for later use. Hourly high temperature test, the weight loss rate is 10.2%;
[0043] With the white carbon black of 60g epoxy group functionalization prepared above, 75g polyhexamethylene guanidine hydrochloride (average molecular weight 10000), 10g polyoxypropylene triol (hydroxyl value 53~59) and 5g me...
Embodiment 2
[0046] Pretreat diatomite (average particle size 20 μm) at 250°C for 4 hours, cool to room temperature, weigh 100 g of diatomite, and add it to a mixed solution of 1000 ml of absolute ethanol / water (volume ratio 1:1), Add dilute acetic acid solution dropwise to make the pH of the mixture 4~5, start stirring and assist the ultrasonic environment to make it uniformly dispersed for 30 minutes, and gradually add 30g of γ-glycidyl etheroxypropyl triethoxysilane (CAS number: 2602- 34-8), then heated up to 70°C, stirred at constant temperature for 10 hours, filtered the diatomite suspension, washed 3 times with absolute ethanol, dried and ground to obtain diatoms functionalized with epoxy groups The soil was preserved for later use, and the sample was placed at 600°C for 5 hours to perform a high-temperature test with a weight loss rate of 7.3%.
[0047] Mix 65g of the epoxy functionalized diatomite prepared above, 70g polyhexamethyleneguanidine hydrochloride (average molecular weigh...
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