CN111286090A - Preparation method of sulfur dispersion for latex sponge - Google Patents

Preparation method of sulfur dispersion for latex sponge Download PDF

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Publication number
CN111286090A
CN111286090A CN201811503937.5A CN201811503937A CN111286090A CN 111286090 A CN111286090 A CN 111286090A CN 201811503937 A CN201811503937 A CN 201811503937A CN 111286090 A CN111286090 A CN 111286090A
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CN
China
Prior art keywords
sulfur
parts
latex sponge
dispersion
latex
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201811503937.5A
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Chinese (zh)
Inventor
何拥军
贾成浩
田勇
刁国旺
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jiangsu Jsy Latex Product Co ltd
Yangzhou University
Original Assignee
Jiangsu Jsy Latex Product Co ltd
Yangzhou University
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Filing date
Publication date
Application filed by Jiangsu Jsy Latex Product Co ltd, Yangzhou University filed Critical Jiangsu Jsy Latex Product Co ltd
Priority to CN201811503937.5A priority Critical patent/CN111286090A/en
Publication of CN111286090A publication Critical patent/CN111286090A/en
Withdrawn legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0095Mixtures of at least two compounding ingredients belonging to different one-dot groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0014Use of organic additives
    • C08J9/0033Use of organic additives containing sulfur
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0066Use of inorganic compounding ingredients
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2307/00Characterised by the use of natural rubber
    • C08J2307/02Latex
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2497/00Characterised by the use of lignin-containing materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/06Sulfur
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/41Compounds containing sulfur bound to oxygen
    • C08K5/42Sulfonic acids; Derivatives thereof

Abstract

A preparation method of sulfur dispersion for latex sponge. Relates to the field of latex industry, in particular to a preparation method of a sulfur dispersion for latex sponge. Provides a preparation method of the sulfur dispersion for the latex sponge, which can improve the performance of the latex sponge and has good dispersion effect. The dispersant is dinaphthyl methane sodium disulfonate or sodium lignosulfonate. The humectant is one or more of a humectant OT, a humectant JFC or a nekal BX. The particle size of the sulfur dispersion is D502.2-4.0 μm and D903.5-8.5 μm. The sulfur, the dispersant, the wetting agent and the water are mixed according to a certain proportion and ground to prepare the sulfur dispersoid.

Description

Preparation method of sulfur dispersion for latex sponge
Technical Field
The invention relates to the field of latex industry, in particular to a preparation method of a sulfur dispersion for latex sponges.
Background
Latex sponge is a low density, porous, open-cell material, also known as a continuous foam of rubber. Latex sponges have many characteristics, such as excellent buffering and decompression performance, compression fatigue resistance, good heat preservation, sound insulation and heat resistance, and are widely applied to the automobile industry, the aviation industry, the chemical industry, medical appliances, sound insulation, shock resistance, heat insulation, sealing, life hygiene, sports goods and other aspects, and have long been the main products in the latex industry, and account for more than half of the total annual latex consumption.
Latex sponges have a variety of vulcanization systems: a sulfur vulcanization system, a thiuram vulcanization system, an organic peroxide vulcanization system, and a radiation vulcanization system. The sulfur vulcanization system is a method mostly adopted in the current latex sponge industrial production, sulfur, vulcanization accelerator and the like enter colloidal particles in a molecular or particle form to be contacted with rubber, and then a vulcanization reaction is quickly carried out on the outer layer of the colloidal particles under the action of temperature, namely, a cross-linking reaction mainly occurs on the surface layer of the particles. The dispersion effect of the sulfur dispersion has great influence on the diffusion of sulfur particles in the emulsion, thereby influencing the vulcanization reaction of colloidal particles and finally influencing the performance of products. Moreover, the sulfur is a strong hydrophobic substance and is not easy to disperse in water, so that the selection of a proper dispersing agent and a proper wetting agent is particularly important. Sodium lignosulfonate is an anionic dispersant and has a large molecular weight. Not only can provide electrostatic repulsion, but also has steric hindrance effect, and can increase sulfur dispersibility and suspension ability. However, sodium lignosulfonate is inferior in reducing surface tension, wettability and permeability, so it is necessary to select a suitable wetting agent to be used in combination therewith.
Disclosure of Invention
Aiming at the problems, the invention provides the preparation method of the sulfur dispersion for the latex sponge, which can improve the performance of the latex sponge and has good dispersion effect.
The technical scheme of the invention is as follows: the method comprises the following steps: according to the mass parts, 45-55 parts of sulfur powder, 1-3 parts of dispersing agent, 0.5-1.5 parts of wetting agent and 46.5-48.5 parts of water are stirred and mixed, and then sanding is carried out for 4-8 hours, thus obtaining the sulfur-containing water-based paint.
The dispersant is dinaphthyl methane sodium disulfonate or sodium lignosulfonate.
The humectant is one or more of a humectant OT, a humectant JFC or a nekal BX.
The particle size of the sulfur dispersion is D502.2-4.0 μm and D903.5-8.5 μm.
The invention has the beneficial effects that: the sulfur, the dispersant, the wetting agent and the water are mixed according to a certain proportion and ground to prepare the sulfur dispersoid. The dispersing agent can improve the good dispersing ability, and the wetting agent can ensure that the dispersing agent can be better contacted with the sulfur, improve the dispersing effect of the dispersing agent and ensure that the sulfur is kept in a uniformly dispersed state in water. Therefore, the method can improve the dispersion effect of the sulfur dispersion, thereby improving the vulcanization effect and quality and further improving the quality of the latex sponge. The wetting agent OT can remarkably reduce surface tension and quickly permeate the surface of sulfur, and can well disperse sulfur and slow down the sedimentation of the sulfur when being matched with sodium lignosulphonate.
Detailed Description
The present invention will be described in detail with reference to examples.
Example 1
45 parts of sulfur and 1 part of sodium dinaphthylmethanedisulfonate, 0.5 part of a wetting agent OT and 46.5 parts of water are mixed and then ground for 4 hours using a sand mill, and the particle size is measured: d502.5 μm, D905.8 μm.
Adding 8 parts of ground sulfur dispersoid and small materials such as potassium oleate into 100 parts of natural latex, performing procedures such as ripening, foaming, vulcanizing, drying and the like to obtain natural latex sponge, and finally performing performance test: tensile strength: 65 kPa, compression set: 8.5 percent.
Example 2
50 parts of sulphur and 2 parts of sodium dinaphthylmethanesulfonate, 1 part of a wetting agent JFC and 48 parts of water are mixed and then ground for 6h using a sand mill, and the particle size is measured: d503.4 μm, D907.6 μm.
Adding 8 parts of ground sulfur dispersoid and small materials such as potassium oleate into 100 parts of natural latex, performing procedures such as ripening, foaming, vulcanizing, drying and the like to obtain natural latex sponge, and finally performing performance test: tensile strength: 47 kPa, compression set: 9.7 percent.
Example 3
55 parts of sulphur and 3 parts of sodium lignosulfonate, 1.5 parts of nekal BX and 48.5 parts of water are mixed and then ground for 8 hours using a sand mill, and the particle size is measured: d503.9 μm, D908.5 μm.
Adding 8 parts of ground sulfur dispersoid and small materials such as potassium oleate into 100 parts of natural latex, performing procedures such as ripening, foaming, vulcanizing, drying and the like to obtain natural latex sponge, and finally performing performance test: tensile strength: 45 kPa, compression set: 10.6 percent.
Example 4
50 parts of sulfur and 1 part of sodium lignosulfonate, 1 part of wetting agent OT, 0.5 part of sodium lignosulfonate and 48 parts of water are mixed and then ground for 6 hours using a sand mill, and the particle size is measured: d502.5 μm, D903.5 μm.
Adding 8 parts of ground sulfur dispersoid and small materials such as potassium oleate into 100 parts of natural latex, performing procedures such as ripening, foaming, vulcanizing, drying and the like to obtain natural latex sponge, and finally performing performance test: tensile strength: 75kPa, compression set: 6.8 percent.
Example 5
50 parts of sulphur and 1 part of sodium lignosulfonate, 1 part of wetting agent JFC and 48 parts of water are mixed and then ground for 5 hours using a sand mill, and the particle size is measured: d502.2 μm, D904.5 μm.
Adding 8 parts of ground sulfur dispersoid and small materials such as potassium oleate into 100 parts of natural latex, performing procedures such as ripening, foaming, vulcanizing, drying and the like to obtain natural latex sponge, and finally performing performance test: tensile strength: 66 kPa, compression set: 8.1 percent.
Example 6
50 parts of sulphur and 1 part of sodium lignosulfonate, 1 part of nekal BX and 48 parts of water are mixed and then ground for 8 hours using a sand mill, and the particle size is tested: d502.9 μm, D905.6 μm.
Adding 8 parts of ground sulfur dispersoid and small materials such as potassium oleate into 100 parts of natural latex, performing procedures such as ripening, foaming, vulcanizing, drying and the like to obtain natural latex sponge, and finally performing performance test: tensile strength: 59 kPa, compression set: 8.9 percent.

Claims (4)

1. The preparation method of the sulfur dispersion for the latex sponge is characterized by comprising the following steps of: according to the mass parts, 45-55 parts of sulfur powder, 1-3 parts of dispersing agent, 0.5-1.5 parts of wetting agent and 46.5-48.5 parts of water are stirred and mixed, and then sanding is carried out for 4-8 hours, thus obtaining the sulfur-containing water-based paint.
2. The method for preparing the sulfur dispersion for the latex sponge according to claim 1, wherein the dispersant is dinaphthylmethane sodium disulfonate or sodium lignosulfonate.
3. The method for preparing the sulfur dispersion for the latex sponge according to claim 1, wherein the wetting agent is one or more of a wetting agent OT, a wetting agent JFC and a nekal BX.
4. The method for preparing the sulfur dispersion for the latex sponge according to claim 1, wherein the particle size of the sulfur dispersion is D502.2-4.0 μm and D903.5-8.5 μm.
CN201811503937.5A 2018-12-10 2018-12-10 Preparation method of sulfur dispersion for latex sponge Withdrawn CN111286090A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811503937.5A CN111286090A (en) 2018-12-10 2018-12-10 Preparation method of sulfur dispersion for latex sponge

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811503937.5A CN111286090A (en) 2018-12-10 2018-12-10 Preparation method of sulfur dispersion for latex sponge

Publications (1)

Publication Number Publication Date
CN111286090A true CN111286090A (en) 2020-06-16

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Country Status (1)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111690183A (en) * 2020-07-17 2020-09-22 江苏金世缘乳胶制品股份有限公司 Production process of mold mattress
CN115612173A (en) * 2022-11-09 2023-01-17 广东金发科技有限公司 Sulfur dispersion liquid and preparation method and application thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111690183A (en) * 2020-07-17 2020-09-22 江苏金世缘乳胶制品股份有限公司 Production process of mold mattress
CN115612173A (en) * 2022-11-09 2023-01-17 广东金发科技有限公司 Sulfur dispersion liquid and preparation method and application thereof
CN115612173B (en) * 2022-11-09 2023-12-01 广东金发科技有限公司 Sulfur dispersion liquid and preparation method and application thereof

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Application publication date: 20200616