Quaternary ammonium salt hyperbranched antistatic agent and preparation method thereof

A technology of antistatic agent and quaternary ammonium salt, applied in the field of quaternary ammonium salt hyperbranched antistatic agent, preparation of the quaternary ammonium salt hyperbranched antistatic agent, and preparation field of quaternary ammonium salt hyperbranched antistatic agent , to achieve the effect of strong water absorption, low comprehensive cost and low production cost

Inactive Publication Date: 2014-06-18
UNIV OF JINAN
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] In order to solve the low molecular weight antistatic agent in the prior art, the stability is not good, the compatibility with the matrix is ​​poor, and the defects such as easy migration are provided by the present invention. A quaternary ammonium salt hyperbranched antistatic agent with good compatibility with the matrix, which can greatly improve the antistatic performance and basically does not affect the physical properties of the matrix

Method used

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  • Quaternary ammonium salt hyperbranched antistatic agent and preparation method thereof
  • Quaternary ammonium salt hyperbranched antistatic agent and preparation method thereof
  • Quaternary ammonium salt hyperbranched antistatic agent and preparation method thereof

Examples

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Embodiment 1

[0041] 1. First prepare the second-generation hydroxyl-terminated hyperbranched G21

[0042] (1) Weigh 9.02g (0.09mol) succinic anhydride, 9.48g (0.09mol) diethanolamine (refluxing and dehydrating before use), first dissolve diethanolamine in 40ml N,N-dimethylacetamide (DMAc), dissolve Then pour it into a three-necked flask equipped with a thermometer, then dissolve succinic anhydride with 40ml of DMAc, then slowly drop it into the three-necked flask, and use a magnetic stirrer to react at 25°C for 2h to obtain AB 2 type monomer;

[0043] (2) Then add 50ml of toluene to the above-mentioned three-necked flask first, then add 1.34g (0.01mol) trimethylolpropane as the nuclear molecule, wait until the trimethylolpropane is completely dissolved, then add 0.15g of sulfamic acid, Stir and heat until there is reflux, separate the generated water with a water separator, stop the reaction after 6 hours of heat preservation, cool down to room temperature, and remove the solvent by rotar...

Embodiment 2

[0049] 1. First prepare the second-generation hydroxyl-terminated hyperbranched G22

[0050] (1) Weigh 9.02g (0.09mol) of succinic anhydride and 4.08g (0.09mol) of diethanolamine (refluxing and dehydrating before use), first dissolve diethanolamine in 40ml of N,N-dimethylacetamide (DMAc), dissolve Then pour it into a three-necked flask equipped with a thermometer and a water separator, then dissolve succinic anhydride with 40ml of DMAc, then slowly drop it into the three-necked flask, and use a magnetic stirrer to react at 25°C for 2 hours to obtain AB 2 type monomer;

[0051] (2) Then add 50mL of toluene to the above-mentioned three-necked flask first, then add 1.34g (0.01mol) trimethylolpropane as the nuclear molecule, wait until the trimethylolpropane is completely dissolved, then add 0.15g of sulfamic acid, Stir and heat until there is reflux, separate the generated water with a water separator, stop the reaction after 6 hours of heat preservation, cool down to room tempe...

Embodiment 3

[0057] 1. First prepare the third-generation hydroxyl-terminated hyperbranched G31

[0058] (1) Weigh 10.51g (0.105mol) of succinic anhydride and 11.04g (0.105mol) of diethanolamine (refluxing and dehydrating before use), first dissolve diethanolamine in 40ml of N,N-dimethylacetamide (DMAc), dissolve Then pour it into a three-necked flask equipped with a thermometer and a water separator, then dissolve succinic anhydride with 40ml of DMAc, then slowly drop it into the three-necked flask, and use a magnetic stirrer to react at 25°C for 3h to obtain AB 2 type monomer;

[0059] (2) Then add 50ml of toluene to the above-mentioned three-necked flask first, then add 0.67g (0.005mol) trimethylolpropane as the nuclear molecule, wait until the trimethylolpropane is completely dissolved, then add 0.18g of sulfamic acid, Stir and heat until there is reflux, separate the generated water with a water separator, react until anhydrous is generated, end the reaction, cool down to room temper...

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Abstract

The invention relates to the technical field of a high polymer material antistatic agent, and particularly relates to a quaternary ammonium salt hyperbranched antistatic agent. Propargyl alcohol reacts with succinic anhydride so as to obtain a modified monomer R1, the R1 reacts with 3-(dimethylamino)-1-propanethiol so as to obtain a modified monomer R2, the R2 reacts with a hydroxyl-terminated hyperbranched polymer so as to obtain a dimethyl amine-terminated hyperbranched structure, and then the dimethyl amine-terminated hyperbranched structure reacts with alkyl chloride so as to obtain the quaternary ammonium salt hyperbranched antistatic agent. The molecules of the antistatic agent contain more effective active groups, the utilization rate of the molecules is relatively high, the surface water absorbability of the antistatic agent in a substrate is relatively strong, and correspondingly the antistatic agent has a relatively good antistatic effect; the antistatic agent has relatively good compatibility with a medium and very good dispersibility.

Description

technical field [0001] The invention relates to the technical field of polymer material antistatic agents, in particular to a quaternary ammonium salt hyperbranched antistatic agent, and also to a preparation method of the quaternary ammonium salt hyperbranched antistatic agent. Background technique [0002] With the continuous development of polymer materials, more and more polymer products are used. In addition to the characteristics of lighter weight compared with inorganic materials, polymers also have better physical properties such as strength. However, since ordinary polymer materials are good insulating materials, the surface is prone to generate static electricity due to friction. If the static electricity is not discharged in time, a large amount of static electricity will generate sparks, which will cause different hazards in different fields. For example, static electricity generated on the surface of plastics may cause problems such as production failure, spar...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08G83/00C08L27/06C08L87/00
Inventor 寿崇琦尤光星张宇矦贵海
Owner UNIV OF JINAN
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