Summary of the invention
The object of this invention is to provide a kind of preparation method of paper grade (stock) water absorbing agent, the preparation method of this paper grade (stock) water absorbing agent can solve water absorbing agent reduces effect problem by the impact of wet strength agent.
In order to solve the problem, the technical solution used in the present invention is:
This paper grade (stock) water absorbing agent is prepared from by the raw material of following parts by weight: polyvinyl alcohol 20 parts ~ 30 parts, starch graft copolymer 23 parts ~ 28 parts, sorbierite 5 parts ~ 10 parts, butanedioic acid 2 parts ~ 6 parts, 1 part ~ 5 parts, sodium carbonate;
Preparation method comprises the following steps: in reactor, add polyvinyl alcohol and starch graft copolymer, be warming up to 40 DEG C ~ 55 DEG C, be stirred to the mixing speed of 400 ~ 600 revs/min and dissolve completely, then add sorbierite, butanedioic acid and sodium carbonate successively, to proceed in Ultrasound Instrument washer ultrasonic 5 minutes ~ 10 minutes, then proceed in reactor, react 5 minutes ~ 10 minutes at being warming up to 30 DEG C ~ 40 DEG C, then continue to be warming up to 45 DEG C ~ 55 DEG C, react 7 minutes ~ 12 minutes, be cooled to room temperature.
Owing to have employed technique scheme, the present invention compared with prior art has following beneficial effect:
This paper grade (stock) water absorbing agent is prepared from by polyvinyl alcohol, starch graft copolymer, sorbierite, butanedioic acid, sodium carbonate, and the water absorbing agent obtained can absorb moisture fast while the wet strength increasing page and dry tensile strength.
Detailed description of the invention
Below in conjunction with embodiment, the invention will be further described:
Embodiment 1
The present embodiment paper grade (stock) water absorbing agent is prepared from by the raw material of following parts by weight: polyvinyl alcohol 20 parts, starch graft copolymer 28 parts, sorbierite 7 parts, butanedioic acid 6 parts, 3 parts, sodium carbonate.
Preparation method comprises the following steps: in reactor, add polyvinyl alcohol and starch graft copolymer, be warming up to 40 DEG C, be stirred to the mixing speed of 500 revs/min and dissolve completely, then add sorbierite, butanedioic acid and sodium carbonate successively, to proceed in Ultrasound Instrument washer ultrasonic 10 minutes, then proceed in reactor, react 10 minutes at being warming up to 30 DEG C, then continue to be warming up to 45 DEG C, react 12 minutes, be cooled to room temperature.
Embodiment 2
The present embodiment paper grade (stock) water absorbing agent is prepared from by the raw material of following parts by weight: polyvinyl alcohol 20 parts, starch graft copolymer 28 parts, sorbierite 7 parts, butanedioic acid 6 parts, 3 parts, sodium carbonate.
Preparation method comprises the following steps: in reactor, add polyvinyl alcohol and starch graft copolymer, be warming up to 55 DEG C, be stirred to the mixing speed of 400 revs/min and dissolve completely, then add sorbierite, butanedioic acid and sodium carbonate successively, to proceed in Ultrasound Instrument washer ultrasonic 7 minutes, then proceed in reactor, react 7 minutes at being warming up to 35 DEG C, then continue to be warming up to 50 DEG C, react 7 minutes, be cooled to room temperature.
Embodiment 3
The present embodiment paper grade (stock) water absorbing agent is prepared from by the raw material of following parts by weight: polyvinyl alcohol 20 parts, starch graft copolymer 28 parts, sorbierite 7 parts, butanedioic acid 6 parts, 3 parts, sodium carbonate.
Preparation method comprises the following steps: in reactor, add polyvinyl alcohol and starch graft copolymer, be warming up to 50 DEG C, be stirred to the mixing speed of 600 revs/min and dissolve completely, then add sorbierite, butanedioic acid and sodium carbonate successively, to proceed in Ultrasound Instrument washer ultrasonic 5 minutes, then proceed in reactor, react 5 minutes at being warming up to 40 DEG C, then continue to be warming up to 55 DEG C, react 10 minutes, be cooled to room temperature.