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Method for preparing organosilicon modified paper sheet humidifying strong agent

A technology of wetting strength agent and organic silicon, which is applied in the field of fine chemical preparation technology, can solve the problems of paper wet strength effect not meeting the production requirements, crosslinking degree, low molecular weight, poor paper uniformity, etc., and achieve improvement Keep the performance, eco-environment and human health friendly, reduce the effect of expansion and deformation

Inactive Publication Date: 2010-07-28
SHAANXI UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since this type of product has not been cross-linked and modified, its cross-linking degree and molecular weight are low, and its retention performance is poor. The wet strength effect of the paper is far from the production requirements, especially for some paper types that require high wet strength. It is still not ideal; at the same time, it will bring many adverse effects to the papermaking, such as the pulp is easy to produce air bubbles, flocculation, poor paper uniformity, low rigidity, etc.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0007] Example 1: Add polyamine diethylenetriamine and dibasic acid succinic acid into a drying reactor at a molar ratio of 1.0:1, heat to 200°C, and keep warm for 5 hours to make the polyamide polyamine in the reactor The viscosity of the product reaches 100mPa.s (the product viscosity is measured at 25°C and the polyamide polyamine has a solid content of 50%). Add deionized water to dilute the polyamide polyamine to a solid content of 50% to obtain humidification Solution A of strong agent intermediate; after mixing solution A, epichlorohydrin and organic silane coupling agent methyltrimethoxysilane in a mass ratio of 100:20:2, add deionized water to dilute the system to contain The solid content is 20%, react at 80°C for 1 hour, when the viscosity of the system reaches 20mPa.s (the product viscosity is measured at 25°C), stop heating, dilute with deionized water to a solid content of 15%, and adjust the system with hydrochloric acid When the pH reaches 1, the organosilicon-...

Embodiment 2

[0008] Example 2: Add polyamine triethylenetetramine and dibasic acid adipic acid into a drying reactor at a molar ratio of 0.8:1, heat to 180°C, and keep warm for 7 hours to make the polyamide polyamine in the reactor The viscosity of the product reaches 150mPa.s (the product viscosity is measured at 25°C and the polyamide polyamine has a solid content of 50%). Add deionized water to dilute the polyamide polyamine to a solid content of 50% to obtain humidification Solution A of strong agent intermediate; after mixing solution A, epichlorohydrin and organic silane coupling agent methyltriethoxysilane according to the mass ratio of 100:5:4, add deionized water to dilute the system to The solid content is 20%, react at 70°C for 3 hours, when the viscosity of the system reaches 30mPa.s (the product viscosity is measured at 25°C), stop heating, dilute with deionized water to a solid content of 12%, and use glacial acetic acid The pH of the system is adjusted to 3, and the silicone...

Embodiment 3

[0009] Example 3: Add the polyamine tetraethylenepentamine and the dibasic acid fumaric acid into the dry reactor at a molar ratio of 1.2:1, heat to 150°C, and keep the temperature for 3 hours to make the polyamide polyamine in the reactor The viscosity of the product reaches 130mPa.s (the product viscosity is measured at 25°C and the polyamide polyamine has a solid content of 50%). Add deionized water to dilute the polyamide polyamine to a solid content of 50% to obtain humidification Solution A of the strong agent intermediate; after mixing solution A, epichlorohydrin and organic silane coupling agent methyltriacetoxysilane in a mass ratio of 100:30:1, add deionized water to dilute the system to The solid content is 20%, react at 60°C for 5 hours, when the viscosity of the system reaches 40mPa.s (the product viscosity is measured at 25°C), stop heating, dilute with deionized water to a solid content of 10%, adjust with formic acid When the pH of the system reaches 2, the org...

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Abstract

The invention discloses a preparation method of a paper wet strengthening agent that is modified by organic silicon, which comprises the following steps: firstly combines the raw materials of dibasic acid and polyhydric amine into a polyamine intermediate compound of daiamid. A certain amount of the polyamine intermediate compound of daiamid, epoxy chloropropane and an organosilane coupling agentare taken to react under certain temperature so as to achieve certain viscosity, and the reaction is halted by adding acid, thus obtaining the paper wet strengthening agent that is modified by organic silicon. The preparation method of the paper wet strengthening agent that is modified by organic silicon can reduce the usage of the epoxy chloropropane and lower the organic chlorine content in discharged substances; the cross-linked product greatly increases molecular weight and active crosslinking points of molecular chain sections. The product of the paper wet strengthening agent that is modified by organic silicon achieves greatly raised retention degree, can improve not only the wet strength of paper but also the paper physical performance such as folding resistance, tensile strength and dry strength, etc., and the superficial water-proof performance of paper can be greatly raised if the paper wet strengthening agent is coated on the surface of paper.

Description

technical field [0001] The invention belongs to the field of preparation technology of fine chemicals, and in particular relates to a preparation method of an organosilicon-modified paper moisturizing strength agent. Background technique [0002] Many paper products, especially industrial papers, require high wet strength. Polyamide polyamine epichlorohydrin (PAE), as the most widely used wet strength agent at present, has advantages that cannot be compared with traditional wet strength agents urea-formaldehyde resin (UF), modified melamine-formaldehyde resin (MF) and acrylamide polymers . It not only has good wet strength effect and repulpability, but also has no free formaldehyde in the production process, which is friendly to the ecological environment and human health. The existing PAE preparation method is usually prepared by reacting adipic acid and diethylenetriamine or triethylenetetramine under alkaline conditions to prepare polyamine, and then reacting with epich...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): D21H21/20
Inventor 费贵强沈一丁王海花
Owner SHAANXI UNIV OF SCI & TECH
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