A latent polythioether-based polythiol, its synthesis method and application
A synthesis method and polysulfide technology, applied in the field of polysulfide-based polymers, can solve the problems affecting the efficient corrosion inhibition performance of corrosion inhibitors, storage conditions, etc., and achieve high yield, simple operation and mild reaction conditions. Effect
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Embodiment 1
[0030] In this embodiment, the structural formula of latent polythioether-based polythiol is:
[0031]
[0032] The preparation method of above-mentioned latent polythioether-based polythiol comprises the steps:
[0033] (1) Add 1 molar portion of propynyl glycidyl ether and 1 molar portion of thioacetic acid successively in the reactor to react to generate alkynyl thioacetate;
[0034] (2) Add 1 mole part of propylene thiol, the alkynyl thioacetate obtained in step (1), and 0.01 mole part of azobisisobutyronitrile in the reactor, and carry out acetyl- Alkyne addition polymerization reaction for 1 hour;
[0035] (3) washing the product obtained in step (2) with dilute hydrochloric acid, evaporating to remove the solvent, and then precipitating and drying to obtain an acetyl compound containing a β-ester group, that is, a latent polythioether-based polythiol;
[0036] figure 1 is the product obtained in the above step (3) 1 H NMR spectrum.
[0037] Dissolve the product ob...
Embodiment 2
[0041] In this embodiment, the structural formula of latent polythioether-based polythiol is:
[0042]
[0043] The preparation method of above-mentioned latent polythioether-based polythiol comprises the steps:
[0044] (1) add 1-alkynyl-4-epoxy pentane of 1 mole part, the thioacetic acid of 1 mole part successively in reactor, react and generate alkynyl thioacetate;
[0045] (2) Add 1 mole part of propylene thiol, the alkynyl thioacetate obtained in step (1), and 0.1 mole part of azobisisobutyronitrile in the reactor, and carry out acetyl- Alkyne addition polymerization reaction for 1 hour;
[0046] (3) The product obtained in step (2) is washed with dilute hydrochloric acid, evaporated to remove the solvent, then precipitated and dried to obtain an acetyl compound containing a β-ester group, that is, a latent polythioether-based polythiol;
[0047] The product obtained in step (3) was dissolved in 10 mole parts of toluene, and 0.1 mole part of N,N-dimethylaniline was a...
Embodiment 3
[0049] In this embodiment, the structural formula of latent polythioether-based polythiol is:
[0050]
[0051] The preparation method of above-mentioned latent polythioether-based polythiol comprises the steps:
[0052] (1) Add 1 molar portion of 2-butyne-3-oxirane and 1 molar portion of thioacetic acid successively in the reactor to react to generate alkynyl thioacetate;
[0053] (2) Add 1 mole part of propylene thiol, the alkynyl thioacetate obtained in step (1), and 0.01 mole part of azobisisobutyronitrile in the reactor, and carry out acetyl- Alkyne addition polymerization reaction for 24 hours;
[0054] (3) The product obtained in step (2) is washed with dilute hydrochloric acid, evaporated to remove the solvent, then precipitated and dried to obtain an acetyl compound containing a β-ester group, that is, a latent polythioether-based polythiol;
[0055] Dissolve the product obtained in step (3) in 10 molar parts of tetrahydrofuran, add 0.5 molar parts of N,N-dipropy...
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