CN113150215A - Preparation method of environment-friendly emulsion for coating synthetic paper - Google Patents

Preparation method of environment-friendly emulsion for coating synthetic paper Download PDF

Info

Publication number
CN113150215A
CN113150215A CN202110503582.5A CN202110503582A CN113150215A CN 113150215 A CN113150215 A CN 113150215A CN 202110503582 A CN202110503582 A CN 202110503582A CN 113150215 A CN113150215 A CN 113150215A
Authority
CN
China
Prior art keywords
mixed monomer
parts
environment
mixed
potassium persulfate
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.)
Pending
Application number
CN202110503582.5A
Other languages
Chinese (zh)
Inventor
王彦华
章圣苗
夏浙安
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.)
East China University of Science and Technology
Original Assignee
East China University of Science and Technology
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by East China University of Science and Technology filed Critical East China University of Science and Technology
Priority to CN202110503582.5A priority Critical patent/CN113150215A/en
Publication of CN113150215A publication Critical patent/CN113150215A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F251/00Macromolecular compounds obtained by polymerising monomers on to polysaccharides or derivatives thereof
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/20Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paper (AREA)

Abstract

A preparation method of environment-friendly emulsion for coating synthetic paper is characterized by comprising the following steps: adding 100 parts of deionized water into the reaction kettle, starting stirring, adding 0.1-0.3 part of sodium dodecyl polyoxyethylene sulfate and 0.1-0.3 part of potassium persulfate, and continuing stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; adding 1-3 parts of styrene, heating to 80 ℃, adding 15-20 parts of oxidized corn starch, and keeping the temperature for 0.5 hour; and slowly adding the mixed monomer A and the mixed monomer B, controlling the mixed monomer A and the mixed monomer B to be dripped simultaneously, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper.

Description

Preparation method of environment-friendly emulsion for coating synthetic paper
Technical Field
The invention relates to a preparation method of environment-friendly emulsion for coating synthetic paper.
Background
The strength of the environment-friendly synthetic paper is higher than that of common plant fiber paper, and the environment-friendly synthetic paper is excellent in tensile strength, tearing strength and tensile strength; the paint has good weather resistance, water resistance, chemical resistance and oil resistance; the environment-friendly synthetic paper can be soaked in water for a long time, has unchanged performance, is not afraid of oil immersion, and has strong resistance to acid, alkali and other solutions; the environment-friendly synthetic paper has good printing effect after being coated on the surface, and the surface is white, non-transparent, uniform in thickness, soft in color tone of a printed product and bright in effect; stable size, no deformation under humid condition, no color change and good appearance retention. The environment-friendly synthetic paper has ink absorbability, so the surface is coated, and the ink absorbability of the coating can be greatly enhanced.
Disclosure of Invention
A preparation method of environment-friendly emulsion for coating synthetic paper is characterized by comprising the following steps: adding 100 parts of deionized water into the reaction kettle, starting stirring, adding 0.1-0.3 part of sodium dodecyl polyoxyethylene sulfate and 0.1-0.3 part of potassium persulfate, and continuing stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; adding 1-3 parts of styrene, heating to 80 ℃, adding 15-20 parts of oxidized corn starch, and keeping the temperature for 0.5 hour; slowly adding the mixed monomer A and the mixed monomer B at the same time, controlling the mixed monomer A and the mixed monomer B to be dripped at the same time, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper;
the mixed monomer A: 10-15 parts of butadiene, 80-90 parts of styrene, 0.2-0.5 part of n-dodecyl mercaptan and 0.5-1.0 part of hydroxyethyl acrylate are uniformly mixed;
the mixed monomer B: 1-3 parts of acrylic acid, 0.4-0.8 part of sodium dodecyl polyoxyethylene sulfate, 0.4-0.8 part of potassium persulfate and 18 parts of deionized water are uniformly mixed.
Detailed Description
Example 1
Adding 100 kg of deionized water into a 2 cubic meter reaction kettle, starting stirring, adding 0.1 kg of sodium dodecyl polyoxyethylene sulfate and 0.1 kg of potassium persulfate, and continuously stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; then adding 1 kg of styrene, heating to 80 ℃, adding 15 kg of oxidized corn starch, and keeping the temperature for 0.5 hour; and slowly adding the mixed monomer A and the mixed monomer B, controlling the mixed monomer A and the mixed monomer B to be dripped simultaneously, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper.
Mixing a monomer A: 10 kg of butadiene, 80 kg of styrene, 0.2 kg of n-dodecyl mercaptan and 0.5 kg of hydroxyethyl acrylate are mixed uniformly.
Mixing a monomer B: 1 kg of acrylic acid, 0.4 kg of sodium dodecyl polyoxyethylene sulfate, 0.4 kg of potassium persulfate and 18 kg of deionized water are uniformly mixed.
Example 2
Adding 100 kg of deionized water into a 2 cubic meter reaction kettle, starting stirring, adding 0.3 kg of sodium dodecyl polyoxyethylene sulfate and 0.3 kg of potassium persulfate, and continuously stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; then adding 3 kg of styrene, heating to 80 ℃, adding 20 kg of oxidized corn starch, and keeping the temperature for 0.5 hour; and slowly adding the mixed monomer A and the mixed monomer B, controlling the mixed monomer A and the mixed monomer B to be dripped simultaneously, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper.
Mixing a monomer A: 15 kg of butadiene, 90 kg of styrene, 0.5 kg of n-dodecyl mercaptan and 1.0 kg of hydroxyethyl acrylate are mixed uniformly.
Mixing a monomer B: 3 kg of acrylic acid, 0.8 kg of sodium dodecyl polyoxyethylene sulfate, 0.8 kg of potassium persulfate and 18 kg of deionized water are uniformly mixed.
Example 3
Adding 100 kg of deionized water into a 2 cubic meter reaction kettle, starting stirring, adding 0.2 kg of sodium dodecyl polyoxyethylene sulfate and 0.2 kg of potassium persulfate, and continuously stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; then adding 2 kg of styrene, heating to 80 ℃, adding 17 kg of oxidized corn starch, and keeping the temperature for 0.5 hour; and slowly adding the mixed monomer A and the mixed monomer B, controlling the mixed monomer A and the mixed monomer B to be dripped simultaneously, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper.
Mixing a monomer A: 13 kg of butadiene, 85 kg of styrene, 0.4 kg of n-dodecyl mercaptan and 0.7 kg of hydroxyethyl acrylate are mixed uniformly.
Mixing a monomer B: 2 kg of acrylic acid, 0.6 kg of sodium dodecyl polyoxyethylene sulfate, 0.6 kg of potassium persulfate and 18 kg of deionized water are uniformly mixed.
Example 4
Adding 100 kg of deionized water into a 2 cubic meter reaction kettle, starting stirring, adding 0.1 kg of sodium dodecyl polyoxyethylene sulfate and 0.3 kg of potassium persulfate, and continuously stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; then adding 3 kg of styrene, heating to 80 ℃, adding 15 kg of oxidized corn starch, and keeping the temperature for 0.5 hour; and slowly adding the mixed monomer A and the mixed monomer B, controlling the mixed monomer A and the mixed monomer B to be dripped simultaneously, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper.
Mixing a monomer A: 15 kg of butadiene, 80 kg of styrene, 0.4 kg of n-dodecyl mercaptan and 1.0 kg of hydroxyethyl acrylate are mixed uniformly.
Mixing a monomer B: 3 kg of acrylic acid, 0.4 kg of sodium dodecyl polyoxyethylene sulfate, 0.8 kg of potassium persulfate and 18 kg of deionized water are uniformly mixed.
Example 5
Adding 100 kg of deionized water into a 2 cubic meter reaction kettle, starting stirring, adding 0.2 kg of sodium dodecyl polyoxyethylene sulfate and 0.1 kg of potassium persulfate, and continuously stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; then adding 2 kg of styrene, heating to 80 ℃, adding 16 kg of oxidized corn starch, and keeping the temperature for 0.5 hour; and slowly adding the mixed monomer A and the mixed monomer B, controlling the mixed monomer A and the mixed monomer B to be dripped simultaneously, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper.
Mixing a monomer A: 12 kg of butadiene, 82 kg of styrene, 0.5 kg of n-dodecyl mercaptan and 0.9 kg of hydroxyethyl acrylate are mixed uniformly.
Mixing a monomer B: 2.3 kg of acrylic acid, 0.5 kg of sodium dodecyl polyoxyethylene sulfate, 0.8 kg of potassium persulfate and 18 kg of deionized water are uniformly mixed.
Example 6
Adding 100 kg of deionized water into a 2 cubic meter reaction kettle, starting stirring, adding 0.3 kg of sodium dodecyl polyoxyethylene sulfate and 0.3 kg of potassium persulfate, and continuously stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; then adding 1 kg of styrene, heating to 80 ℃, adding 19 kg of oxidized corn starch, and keeping the temperature for 0.5 hour; and slowly adding the mixed monomer A and the mixed monomer B, controlling the mixed monomer A and the mixed monomer B to be dripped simultaneously, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper.
Mixing a monomer A: 15 kg of butadiene, 90 kg of styrene, 0.5 kg of n-dodecyl mercaptan and 0.5 kg of hydroxyethyl acrylate are mixed uniformly.
Mixing a monomer B: 2 kg of acrylic acid, 0.7 kg of sodium dodecyl polyoxyethylene sulfate, 0.6 kg of potassium persulfate and 18 kg of deionized water are uniformly mixed.

Claims (1)

1. A preparation method of environment-friendly emulsion for coating synthetic paper is characterized by comprising the following steps: adding 100 parts of deionized water into the reaction kettle, starting stirring, adding 0.1-0.3 part of sodium dodecyl polyoxyethylene sulfate and 0.1-0.3 part of potassium persulfate, and continuing stirring until the sodium dodecyl polyoxyethylene sulfate and the potassium persulfate are completely dissolved; adding 1-3 parts of styrene, heating to 80 ℃, adding 15-20 parts of oxidized corn starch, and keeping the temperature for 0.5 hour; slowly adding the mixed monomer A and the mixed monomer B at the same time, controlling the mixed monomer A and the mixed monomer B to be dripped at the same time, heating to 90 ℃ after dripping, and preserving heat for 1 hour at the temperature to obtain the environment-friendly emulsion for coating the synthetic paper;
the mixed monomer A: 10-15 parts of butadiene, 80-90 parts of styrene, 0.2-0.5 part of n-dodecyl mercaptan and 0.5-1.0 part of hydroxyethyl acrylate are uniformly mixed;
the mixed monomer B: 1-3 parts of acrylic acid, 0.4-0.8 part of sodium dodecyl polyoxyethylene sulfate, 0.4-0.8 part of potassium persulfate and 18 parts of deionized water are uniformly mixed.
CN202110503582.5A 2021-05-10 2021-05-10 Preparation method of environment-friendly emulsion for coating synthetic paper Pending CN113150215A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110503582.5A CN113150215A (en) 2021-05-10 2021-05-10 Preparation method of environment-friendly emulsion for coating synthetic paper

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110503582.5A CN113150215A (en) 2021-05-10 2021-05-10 Preparation method of environment-friendly emulsion for coating synthetic paper

Publications (1)

Publication Number Publication Date
CN113150215A true CN113150215A (en) 2021-07-23

Family

ID=76874056

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110503582.5A Pending CN113150215A (en) 2021-05-10 2021-05-10 Preparation method of environment-friendly emulsion for coating synthetic paper

Country Status (1)

Country Link
CN (1) CN113150215A (en)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101125902A (en) * 2007-09-05 2008-02-20 溧阳市巨神化学品有限公司 Method for preparing carboxylic styrene butadiene latex for carpet back coating
CN104558439A (en) * 2015-01-14 2015-04-29 日照广大建筑材料有限公司 Carboxylic butadiene-styrene latex for textured paper and preparation method thereof
CN106471014A (en) * 2014-07-04 2017-03-01 巴斯夫欧洲公司 Amyloid polymeric dispersions in small, broken bits, its preparation method and the purposes as sizing material in papermaking
CN108677605A (en) * 2018-06-11 2018-10-19 华东理工大学 A kind of Cypres and preparation method thereof
CN108690169A (en) * 2018-06-11 2018-10-23 华东理工大学 A kind of preparation method of Cypres
CN111019034A (en) * 2019-11-20 2020-04-17 上海东升新材料有限公司 Butadiene-styrene latex for base coating and preparation method thereof
CN111995712A (en) * 2020-08-28 2020-11-27 上海东升新材料有限公司 High-solid-content styrene-butadiene latex as well as preparation method and application thereof

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101125902A (en) * 2007-09-05 2008-02-20 溧阳市巨神化学品有限公司 Method for preparing carboxylic styrene butadiene latex for carpet back coating
CN106471014A (en) * 2014-07-04 2017-03-01 巴斯夫欧洲公司 Amyloid polymeric dispersions in small, broken bits, its preparation method and the purposes as sizing material in papermaking
CN104558439A (en) * 2015-01-14 2015-04-29 日照广大建筑材料有限公司 Carboxylic butadiene-styrene latex for textured paper and preparation method thereof
CN108677605A (en) * 2018-06-11 2018-10-19 华东理工大学 A kind of Cypres and preparation method thereof
CN108690169A (en) * 2018-06-11 2018-10-23 华东理工大学 A kind of preparation method of Cypres
CN111019034A (en) * 2019-11-20 2020-04-17 上海东升新材料有限公司 Butadiene-styrene latex for base coating and preparation method thereof
CN111995712A (en) * 2020-08-28 2020-11-27 上海东升新材料有限公司 High-solid-content styrene-butadiene latex as well as preparation method and application thereof

Similar Documents

Publication Publication Date Title
CN102643588B (en) Holographic laser cold-turning gold stamping transfer coating composition and preparation method thereof
CN101225623B (en) Surface sizing agent for paper making
CN104532660A (en) Nano-microcrystalline cellulose paint, preparation method thereof, and coated paper prepared using nano-microcrystalline cellulose paint
CN101649153A (en) Organic silicon modified acrylic ester aqueous wood lacquer latex and synthesizing method thereof
CN104389237A (en) Papermaking coating biomass adhesive, preparation method and applications thereof
WO2013086863A1 (en) Spared sizing direct spray reactive dye ink
CN101088781A (en) Process of making glass etching and silver plating ornament picture
CN113150215A (en) Preparation method of environment-friendly emulsion for coating synthetic paper
CN109705257B (en) Humidity-adjusting acrylic emulsion and preparation method thereof
CN111070952A (en) Ceramic-glazed pearlescent relief color paper and manufacturing method thereof
CN102585081A (en) Rheology modifying agent and preparation method thereof
CN104558384A (en) Special waterborne acrylic resin for wallpaper as well as preparation method of special waterborne acrylic resin
CN102876266B (en) Preparation method of environment-friendly adhesive for lithium ion battery
CN111364284A (en) Modified sizing starch, surface sizing liquid, and preparation method and application thereof
CN103334339A (en) Positive ion styrene-acrylic emulsion surface sizing agent with high reactivity for papermaking and synthetic method thereof
CN101161929B (en) Paint for coating chromatic bobbin printed sheet and preparation method thereof
CN114316124A (en) Preparation method of high-gloss water-based varnish for wood grain paper
CN111303307B (en) Modified sizing starch, surface sizing liquid, and preparation method and application thereof
CN113801263A (en) Silicone-acrylic emulsion for base paint for multicolor paint and preparation method thereof
CN109400809A (en) Different monooctyl ester surface water resistant sizing agent of styrene-t and preparation method thereof
CN111944406A (en) Antistatic color aluminum plate and production process thereof
CN1072227A (en) The coating composition of coated paper
CN116082999A (en) Styrene-acrylic emulsion wallpaper adhesive and preparation method and application thereof
CN109629334A (en) A kind of sizing agent and its preparation process for corrugated paper
CN116731572A (en) Preparation method of green low-carbon energy-saving light real stone paint

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20210723