Modified cellulose and application thereof
A cellulose and modification technology, which is applied to modified cellulose and its application fields, can solve the problems of single effect, decreased color absorption ability of color absorbing sheets, and reduced anti-cross-color effect, etc., and achieves the effect of effective bacteriostatic effect.
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Embodiment 2-1
[0040] 1. Synthesis of (4-vinylphenyl-4'-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone
[0041] The monomer vinyl pyrrolidone (NVP) is prepared into an aqueous solution with a mass fraction of 45%, and a small amount of hydrogen peroxide (0.2% NVP) is used as a catalyst. Under the action of azobisisobutyronitrile (0.3% NVP), The polymerization is initiated at 40-50°C and reacted for 2 hours, and the monomer polymerization conversion rate is 93-95%. Add the (4-vinylphenyl-4'-methylenecarboxyphenyl) iodonium (amount of 0.5% NVP) prepared in Example 1-1, react for 0.2 hours, and block the polymer. (4-vinylphenyl-4'-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone is obtained.
[0042] Then add 0.2% ammonia water to the polymer to decompose the remaining azobisisobutyronitrile. The polymer was spray-dried under hot air at 120-135°C to obtain powdery (4-vinylphenyl-4'-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone. The blocking ra...
Embodiment 2-2
[0053] 1. Synthesis of (4-vinylphenyl-4'-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone
[0054] The monomer vinyl pyrrolidone (NVP) is prepared into an aqueous solution with a mass fraction of 50%. Using a small amount of hydrogen peroxide (0.3% of NVP) as a catalyst, under the action of azobisisobutyronitrile (0.4% of NVP), polymerization was initiated at 50-60°C and reacted for 3 hours. The monomer polymerization conversion rate was 96~98%. Add the ((4-vinylphenyl-4-methylenecarboxyphenyl) iodonium (amount of 0.8% NVP) prepared in Example 1-1, react for 0.5 hours, The compound is capped to obtain (4-vinylphenyl-4-methylenecarboxyphenyl) iodonium capped polyvinylpyrrolidone.
[0055] Then 0.3% ammonia water was added to the polymer to decompose the remaining azobisisobutyronitrile. The polymer is spray-dried under hot air at 135-150°C to obtain powdery (4-vinylphenyl-4-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone. The blocking rate of (4-...
Embodiment 2-3
[0061] 1. Synthesis of (4-vinylphenyl-4'-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone
[0062] The monomer vinyl pyrrolidone (NVP) was prepared into an aqueous solution with a mass fraction of 55%. Using a small amount of hydrogen peroxide (0.4% NVP) as a catalyst, under the action of azobisisobutyronitrile (0.5% NVP), polymerization was initiated at 60-70°C, reacted for 4 hours, and the monomer polymerization conversion rate was 97 ~99%. Add (4-vinylphenyl-4-methylenecarboxyphenyl) iodonium (1% NVP) prepared in Example 1-2, react for 0.6 hours, and block the polymer to obtain (4-Vinylphenyl-4-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone.
[0063] Then 0.4% ammonia water was added to the polymer to decompose the remaining azobisisobutyronitrile. The polymer is spray-dried under hot air at 150-165°C to obtain powdery (4-vinylphenyl-4-methylenecarboxyphenyl) iodonium-terminated polyvinylpyrrolidone. The blocking rate of (4-vinylphenyl-4'-m...
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