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Method for synthesizing graft polymer type amphoteric dry strength agent

The technology of graft polymer and dry strength agent is applied in the field of preparation of graft polymer type amphoteric dry strength agent, and can solve the problems of high cost of synthetic dry strength agent, too large or too small polymer, and high price. To achieve excellent paper dry enhancement effect, good effect and low cost effect

Active Publication Date: 2017-10-10
SHANGHAI DONGSHENG NEW MATERIALS +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The method of adding a cross-linking agent is often used to obtain a branched-chain dry strength agent, but there is often a common problem, that is, the problem of controlling the reaction process. The viscosity of the obtained polymer often appears too large or too small, and improper control often causes problems. Gelation occurs
Due to the high price of the various monomers used, the cost of the current synthetic dry strength agent is relatively high

Method used

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  • Method for synthesizing graft polymer type amphoteric dry strength agent
  • Method for synthesizing graft polymer type amphoteric dry strength agent
  • Method for synthesizing graft polymer type amphoteric dry strength agent

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Add 350g of water to the reaction kettle, add 35g of anionic starch under stirring, heat to 75°C for gelatinization for 2 hours, then add 87g of acrylamide, 16g of methacryloyloxyethyltrimethylammonium chloride, dimethylacrylic acid Amide 1g, mercaptoethanol 0.6g, hydroxypropyl acrylate 3g, ethyl acrylate 1.5g and benzophenone 0.6g were stirred evenly, and 55g of water was added to rinse the feeding port, and the reactor was repeatedly evacuated and nitrogen evacuated 2 to 3 times, and then Maintain nitrogen flow, raise the temperature of the reactor to 85°C, irradiate the reaction system with ultraviolet light, and react for 1.5 hours while maintaining a constant temperature. After that, take samples every 20 minutes for viscosity testing, and stop irradiating ultraviolet light after the viscosity reaches 7000mP*s Light, add 1g of liquid caustic soda (32%) to adjust the pH to 4-6, finally add 0.01g of hydroquinone, add water to adjust the solid content to 20±1%, which i...

Embodiment 2

[0030] Add 350g of water to the reaction kettle, add 58g of anionic starch under stirring, heat to 85°C for gelatinization for 1 hour, then add 58g of acrylamide, 5g of dimethylaminoethyl (meth)acrylate, and 0.08 methylenebisacrylamide g, 0.8 g of ethyl mercaptoacetate, 15 g of hydroxypropyl acrylate, 5 g of styrene and 0.5 g of benzophenone were stirred evenly, and the feeding port was rinsed with 50 g of water, and the reactor was repeatedly evacuated and nitrogen evacuated for 2 to 3 times, and then maintained Nitrogen was passed, the temperature of the reactor was raised to 75°C, and the reaction system was irradiated with ultraviolet light, and the reaction was kept at a constant temperature for 2 hours. After that, samples were taken every 20 minutes for viscosity testing. After the viscosity reached 5000mP*s, stop irradiating ultraviolet light. , add 1g of liquid caustic soda (32%) to adjust the pH to 4-6, finally add 2g of sodium bisulfite, add water to adjust the solid...

Embodiment 3

[0032]Add 450g of water to the reaction kettle, add 40g of anionic starch under stirring, heat to 95°C for gelatinization for 0.5 hours, then add 51g of acrylamide, 5g of methacryloyloxyethyltrimethylammonium chloride, methylenebis 0.03g of acrylamide, 0.2g of mercaptoethanol, 4g of methyl methacrylate, 1g of hydroxypropyl acrylate, 1g of ethyl acrylate and 0.5g of benzophenone, stir evenly, rinse the feeding port with 70g of water, and repeatedly evacuate the reaction kettle Nitrogen was passed for 2 to 3 times, and then the nitrogen was maintained. The temperature of the reactor was raised to 85°C, and the reaction system was irradiated with ultraviolet light. The reaction was kept at a constant temperature for 1.5 hours, and then samples were taken every 20 minutes for viscosity testing. After reaching 6500mP*s, stop irradiating ultraviolet light, adjust the pH to 4-6, and finally add 0.01g of p-benzoquinone, add water to adjust the solid content to 15±1%, which is the final...

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Abstract

The invention provides a method for synthesizing a graft polymer type amphoteric dry strength agent. body, chain transfer agent, other functional monomers and photoinitiators, in an oxygen-free environment, raise the temperature to 70-95°C, irradiate the reaction system with ultraviolet light for 1-2 hours, and then take samples at regular intervals. Viscosity test, after the viscosity reaches 4000-9000mP*s, stop irradiating ultraviolet light, add a pH adjuster to adjust the pH to 4-6, and add a free radical scavenger to obtain the dry strength agent. The dry strength agent synthesized by the method has the characteristics of less dosage, good effect and low cost. It can be used in the production of various paper types such as boxboard paper, corrugated base paper, coated paper, bobbin paper, special paper, etc., to increase the dry strength of paper, especially when recycled waste paper pulp is used as the raw material for papermaking. more pronounced.

Description

technical field [0001] The invention relates to a preparation method of a graft polymer type amphoteric dry strength agent. Background technique [0002] Dry strength agent is an important class of chemicals in the paper industry to increase the strength of paper. It is usually used to compensate for the decrease in paper strength caused by adding fillers or low-grade fibers (such as recycled fibers). Many water-soluble polymers capable of forming hydrogen bonds with fibers can be used as dry strength agents. [0003] In recent years, the utilization rate of waste paper resources in my country has been increasing year by year, and the development potential is huge. However, the increase in the utilization rate of waste paper means the increase in the number of waste paper recycling, which will cause a sharp drop in the paper strength index, so it is necessary to add a dry strength agent to enhance the paper strength. With the increasing demand for paper and paperboard in t...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08F251/00C08F220/56C08F220/34C08F220/54C08F220/28C08F220/18C08F222/38C08F212/08C08F220/14C08F2/48C08F2/38D21H21/18D21H17/41
Inventor 施晓旦金霞朝
Owner SHANGHAI DONGSHENG NEW MATERIALS