CN105419650A - Production process of brightener - Google Patents

Production process of brightener Download PDF

Info

Publication number
CN105419650A
CN105419650A CN201510985452.4A CN201510985452A CN105419650A CN 105419650 A CN105419650 A CN 105419650A CN 201510985452 A CN201510985452 A CN 201510985452A CN 105419650 A CN105419650 A CN 105419650A
Authority
CN
China
Prior art keywords
mass parts
parts
powder
mixed solution
water content
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
CN201510985452.4A
Other languages
Chinese (zh)
Inventor
钱文华
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.)
Changshu Yudong Phosphide Material Co Ltd
Original Assignee
Changshu Yudong Phosphide Material Co Ltd
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 Changshu Yudong Phosphide Material Co Ltd filed Critical Changshu Yudong Phosphide Material Co Ltd
Priority to CN201510985452.4A priority Critical patent/CN105419650A/en
Publication of CN105419650A publication Critical patent/CN105419650A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09GPOLISHING COMPOSITIONS; SKI WAXES
    • C09G1/00Polishing compositions
    • C09G1/06Other polishing compositions
    • C09G1/14Other polishing compositions based on non-waxy substances
    • C09G1/16Other polishing compositions based on non-waxy substances on natural or synthetic resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Detergent Compositions (AREA)
  • Paper (AREA)

Abstract

The invention discloses a production process of a brightener, which includes the following steps: 1) dissolving 28.6 parts of anhydrous disodium hydrogen phosphate in water to prepare a disodium hydrogen phosphate water solution being 45.5% in concentration; 2) successively adding 1-2 parts of carboxymethylcellulose, 0.5 parts of lauryl trimethyl ammonium sulfate, 0.8 parts of methyl triethoxyl silane, 1.1 parts of polyoxyethylene ether, 1.3 parts of sodium tetraborate, 0.9 parts of zinc oxide, 2.2 parts of fluosilicic acid and 1.9 parts of methanol to the disodium hydrogen phosphate water solution to prepare a mixed solution; 3) heating the mixed solution to 64.5 DEG C and fully stirring the mixed solution to obtain white powder being lower than 2% in water content; and 4) continuously stirring the poser at 75.5 DEG C with addition of 1.1 parts of phosphoric acid, 1.2 parts of benzoic acid, 0.9 parts of ammonium chloride, and 0.8 parts of N-lauryl-1,3-propylenediamine, and continuously stirring the powder until the water content is lower than 1%. The brightener is good in dispersing stability and can be storage for a long time.

Description

The production technique of brightening agent
Technical field
The present invention relates to the production technique of brightening agent.
Background technology
The dispersion stabilization of existing surface conditioner has much room for improvement, and can not preserve for a long time.
Summary of the invention
The object of the present invention is to provide a kind of production technique of brightening agent, its surface conditioner dispersion stabilization prepared is excellent, can preserve for a long time.
For achieving the above object, technical scheme of the present invention designs a kind of production technique of brightening agent, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 1 ~ 2 mass parts carboxymethyl cellulose, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
Preferably, the production technique of brightening agent, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 1 mass parts carboxymethyl cellulose, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
Preferably, the production technique of brightening agent, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 2 mass parts carboxymethyl celluloses, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
Advantage of the present invention and beneficial effect are: the production technique providing a kind of brightening agent, and its surface conditioner dispersion stabilization prepared is excellent, can preserve for a long time.
Embodiment
Below in conjunction with embodiment, the specific embodiment of the present invention is further described.Following examples only for technical scheme of the present invention is clearly described, and can not limit the scope of the invention with this.
The technical scheme that the present invention specifically implements is:
Embodiment 1
A production technique for brightening agent, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 1 ~ 2 mass parts carboxymethyl cellulose, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
Embodiment 2
The production technique of brightening agent, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 1 mass parts carboxymethyl cellulose, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
Embodiment 3
The production technique of brightening agent, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 2 mass parts carboxymethyl celluloses, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
The above is only the preferred embodiment of the present invention; it should be pointed out that for those skilled in the art, under the prerequisite not departing from the technology of the present invention principle; can also make some improvements and modifications, these improvements and modifications also should be considered as protection scope of the present invention.

Claims (3)

1. the production technique of brightening agent, is characterized in that, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 1 ~ 2 mass parts carboxymethyl cellulose, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
2. the production technique of brightening agent according to claim 1, is characterized in that, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 1 mass parts carboxymethyl cellulose, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
3. the production technique of brightening agent according to claim 1, is characterized in that, comprises the steps to comprise the steps:
1) the light disodium of 28.6 mass parts anhydrous phosphoric acid is made the aqueous solution that concentration is 45.5%;
2) 2 mass parts carboxymethyl celluloses, 0.5 mass parts trimethyl ammonium sulfate, 0.8 mass parts Union carbide A-162,1.1 mass parts Soxylat A 25-7s, 1.3 mass parts sodium tetraborates, 0.9 mass parts zinc oxide, 2.2 mass parts silicofluoric acid, 1.9 mass parts Methanol are joined in the aqueous solution of Sodium phosphate dibasic successively, obtain mixed solution;
3) mixed solution be heated to 64.5 DEG C and fully stir, obtaining the white powder of water content less than 2%;
4) continue to stir powder at 75.5 DEG C, simultaneously in powder, add 1.1 mass parts phosphoric acid, 1.2 mass parts phenylformic acid, 0.9 mass parts ammonium chloride, 0.8 mass parts N-dodecyl-1,3-trimethylene diamines, then continue stirring and be dried to water content and be less than 1%.
CN201510985452.4A 2015-12-25 2015-12-25 Production process of brightener Pending CN105419650A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510985452.4A CN105419650A (en) 2015-12-25 2015-12-25 Production process of brightener

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510985452.4A CN105419650A (en) 2015-12-25 2015-12-25 Production process of brightener

Publications (1)

Publication Number Publication Date
CN105419650A true CN105419650A (en) 2016-03-23

Family

ID=55498205

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510985452.4A Pending CN105419650A (en) 2015-12-25 2015-12-25 Production process of brightener

Country Status (1)

Country Link
CN (1) CN105419650A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102634285A (en) * 2012-03-27 2012-08-15 河北永泰柯瑞特化工有限公司 Fur brightener composition and preparation method and application thereof
CN103451948A (en) * 2013-08-21 2013-12-18 吴江市七都镇庙港雅迪针织制衣厂 Wool brightener and preparation method thereof
CN103555440A (en) * 2013-10-30 2014-02-05 合肥市华美光电科技有限公司 Corrosion-resistant and bactericidal printed circuit board cleaning agent and preparation method thereof
CN104327745A (en) * 2014-10-19 2015-02-04 青岛文晟汽车零部件有限公司 Efficient leather brightener

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102634285A (en) * 2012-03-27 2012-08-15 河北永泰柯瑞特化工有限公司 Fur brightener composition and preparation method and application thereof
CN103451948A (en) * 2013-08-21 2013-12-18 吴江市七都镇庙港雅迪针织制衣厂 Wool brightener and preparation method thereof
CN103555440A (en) * 2013-10-30 2014-02-05 合肥市华美光电科技有限公司 Corrosion-resistant and bactericidal printed circuit board cleaning agent and preparation method thereof
CN104327745A (en) * 2014-10-19 2015-02-04 青岛文晟汽车零部件有限公司 Efficient leather brightener

Similar Documents

Publication Publication Date Title
CN104193839B (en) Cationic starch and its preparation method and application
CN104448075B (en) For the method preparing heat stability Kynoar
CN106718741A (en) A kind of pH value adjusting method of water planting romaine lettuce factorial praluction nutrient solution
CN105419650A (en) Production process of brightener
CN106243232B (en) A kind of high-performance wet end additive and preparation method thereof
CN105525280A (en) Processing method of phosphorization materials
CN112876126A (en) Powder instant alkali-free accelerator and preparation method thereof
CN102653921A (en) Alkali-resisting penetrating agent for cotton fabric mercerization
CN104231974A (en) Adhesive for cigarettes and preparation method of adhesive
CN103086421B (en) The oxidation sludge that utilization produces when producing stannous sulfate and the anode sludge prepare the method for sodium stannate
CN102363938B (en) Surface sizing agent and preparation method thereof
CN105369233A (en) Preparation method for metal surface regulator
CN105483679A (en) Preparing method for phosphatizing material
LT2013007A (en) Process for preparing compound fertilizer
CN105624660A (en) Method for preparing phosphating material
CN102849975A (en) Metal soap waterproof agent
CN105369607A (en) Preparation method of ultrahigh strength polyethylene fiber
CN104311499A (en) Method for treating chlorine generated in production of metal lithium and application thereof
CN105463441A (en) Preparing method for manganese series phosphatisation surface conditioning agent
CN108545701A (en) A kind of high-efficiency hydrochloric parsing is broken to boil agent and its application
CN109456627A (en) A kind of fireproof flame-retardant coating and preparation method thereof
CN104368115A (en) Efficient fire extinguishing agent and preparation method thereof
CN103755194A (en) Preparation method of aerated concrete reinforcement preservative
CN107261179A (en) A kind of air sterillization aromatic
CN105421073A (en) Sofa fabric

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20160323