A kind of preparation method of europium-based multi-ligand vulcanization accelerator
A vulcanization accelerator and multi-ligand technology, which is applied in the synthesis field of europium-based multi-ligand vulcanization accelerators, can solve problems such as poor solubility, and achieve the effects of simplifying the process, simplifying the feeding process, and achieving a remarkable vulcanization acceleration effect.
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Embodiment 1
[0043] The preparation method of accelerator:
[0044] 0.01molEuCl 3 Dissolve in absolute ethanol at 60°C, dissolve 0.02mol N-cyclohexyl-2-benzothiazole sulfenamide in absolute ethanol solution at 60°C, dissolve 0.01mol citric acid in absolute ethanol at 60°C in solution. Fully mix the ethanol solution of N-cyclohexyl-2-benzothiazole sulfenamide and the ethanol solution of citric acid to obtain a mixed solution. Then the above mixed solution was added dropwise to EuCl 3 in anhydrous ethanol solution, stirred in an oil bath at 80°C for 6h and filtered, and the precipitate was washed with anhydrous ethanol, and placed in CaCl 2 Dry in a desiccant desiccator at 20°C to constant mass to obtain a light yellow powder, the target product EuA 2 B 0 C 0 D. 1 .
Embodiment 2
[0046] The preparation method of accelerator:
[0047] 0.01molEuCl 3 Dissolve in absolute ethanol at 60°C, dissolve 0.0001mol N-cyclohexyl-2-benzothiazole sulfenamide in absolute ethanol solution at 60°C, dissolve 0.02mol potassium ethyl xanthate in 60°C 0.03mol stearic acid is dissolved in the absolute ethanol solution of 60 ℃. Fully mix the ethanol solution of N-cyclohexyl-2-benzothiazole sulfenamide, the ethanol solution of potassium ethyl xanthate and the ethanol solution of stearic acid to obtain a mixed solution. Then the above mixed solution was added dropwise to EuCl 3 in anhydrous ethanol solution, stirred in an oil bath at 80°C for 6h and filtered, and the precipitate was washed with anhydrous ethanol, and placed in CaCl 2Dry in a desiccant desiccator at 20°C to constant mass to obtain a yellow powder, which is the target EuA 0.01 B 2 C 3 D. 0 .
Embodiment 3
[0049] The preparation method of accelerator:
[0050] 0.01molEuCl 3 Dissolve in absolute ethanol at 60°C, dissolve 0.01mol N-cyclohexyl-2-benzothiazole sulfenamide in absolute ethanol solution at 60°C, dissolve 0.01mol potassium ethyl xanthate in 60°C 0.015mol stearic acid was dissolved in the absolute ethanol solution at 60°C, and 0.005mol citric acid was dissolved in the absolute ethanol solution at 60°C. Fully mix the ethanol solution of N-cyclohexyl-2-benzothiazole sulfenamide, the ethanol solution of potassium ethyl xanthate, the ethanol solution of stearic acid and the ethanol solution of citric acid to obtain a mixed solution. Then the above mixed solution was added dropwise to EuCl 3 in anhydrous ethanol solution, stirred in an oil bath at 80°C for 6h and filtered, and the precipitate was washed with anhydrous ethanol, and placed in CaCl 2 Dry in a desiccant desiccator at 20°C to constant mass to obtain a yellow powder, the target product EuA 1 B 1 C 1.5 D. 0.5...
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