CN101029235A - Production of electron triammonium polyphosphate fire retardant - Google Patents

Production of electron triammonium polyphosphate fire retardant Download PDF

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Publication number
CN101029235A
CN101029235A CN 200610008190 CN200610008190A CN101029235A CN 101029235 A CN101029235 A CN 101029235A CN 200610008190 CN200610008190 CN 200610008190 CN 200610008190 A CN200610008190 A CN 200610008190A CN 101029235 A CN101029235 A CN 101029235A
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China
Prior art keywords
electron
polyphosphate
production
fire retardant
triammonium
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Pending
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CN 200610008190
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Chinese (zh)
Inventor
吴良恒
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LULING CHEMICAL CO Ltd JIANGSU
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LULING CHEMICAL CO Ltd JIANGSU
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Application filed by LULING CHEMICAL CO Ltd JIANGSU filed Critical LULING CHEMICAL CO Ltd JIANGSU
Priority to CN 200610008190 priority Critical patent/CN101029235A/en
Publication of CN101029235A publication Critical patent/CN101029235A/en
Pending legal-status Critical Current

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Abstract

Production of fire retardant for electronic products is carried out by taking wet phosphoric acid as initial raw material, reacting it with ammonia to prepare ammonium dibasic phosphate, grinding for ammonium dibasic phosphate and phosphorus pentoxide while mixing, putting them into kneading kettle, adding into ammonia to polymerize, raising temperature by three-stage process, polymerizing and modifying for polymonium phosphate surface by polyurethane coating material to obtain 500-mesh electronic fire retardant.

Description

A kind of production of electron triammonium polyphosphate fire retardant
Technical field
The present invention relates to phosphoric acid by wet process to make the manufacture method of electronic industry triammonium polyphosphate as starting raw material.
Background technology
Ammonium polyphosphate (APP) is that a kind of most important phosphorus that develops rapidly in recent years is inorganic combustion inhibitor, is one of main component of expansion type flame retardant (IFR), can be applicable to fields such as electronics, electrical equipment and automobile.China is from the twentieth century APP that begins one's study the eighties, and industrial scale is less at present, and the polymerization degree is low, and the quality instability can't satisfy the requirement that electronic industry is used.
Summary of the invention
The present invention with phosphoric acid by wet process as starting raw material, obtain Secondary ammonium phosphate with ammonia gas react and the Vanadium Pentoxide in FLAKES polymerization adds ammonia, utilize and mediate reactor and three sections intensification polymerization techniques, avoided dashing material, again modification is carried out on the ammonium polyphosphate surface, obtained electron triammonium polyphosphate fire retardant.
Technical scheme of the present invention is:
1. with phosphoric acid by wet process as starting raw material, get Secondary ammonium phosphate with ammonia gas react.
2. Secondary ammonium phosphate and Vanadium Pentoxide in FLAKES add ammonia and adopt three sections to heat up 170 ℃-180 ℃ through mediating the still polymerization, and 220 ℃-230 ℃, 290-300 ℃ of polymerization technique.
3. adopt the urethane coating material that modification is carried out on the ammonium polyphosphate surface.
With phosphoric acid by wet process as starting raw material, can with the integrated production of phosphorus ammonium, low to ingredient requirement, heat energy, waste residue, waste liquid, waste gas can be used for chemical fertilizers production workshop section in the production process, the process of producing product energy consumption is low, and the product cut size of production can reach 500 orders, and can carry out serialization production.
Specific embodiments
Earlier with phosphoric acid by wet process as starting raw material, produce Secondary ammonium phosphate with ammonia gas react, Secondary ammonium phosphate and Vanadium Pentoxide in FLAKES drop into after ground and mixed mediates still ammonification gas-phase (co-) polymerisation, adopt three sections to heat up 170 ℃-180 ℃, 220 ℃-230 ℃, 290-300 ℃ of polymerization technique polymerization obtains the ammonium polyphosphate particle, adopts the urethane coating material that modification is carried out on the ammonium polyphosphate surface again, obtains particle diameter and can reach 500 purpose electron triammonium polyphosphate fire retardants.
Figure of description is that production unit is mediated the polymeric kettle structure iron.

Claims (2)

1, a kind of production of electron triammonium polyphosphate fire retardant, it is characterized by with Secondary ammonium phosphate and Vanadium Pentoxide in FLAKES ground and mixed, after mediating still ammonification gas-phase (co-) polymerisation, with the urethane coating material modification is carried out on the ammonium polyphosphate surface again, obtained electron triammonium polyphosphate and hinder right agent.
2, production of electron triammonium polyphosphate fire retardant according to claim 1, its feature: earlier with phosphoric acid by wet process as starting raw material, produce Secondary ammonium phosphate with ammonia gas react, Secondary ammonium phosphate and Vanadium Pentoxide in FLAKES ground and mixed input are mediated still ammonification gas-phase (co-) polymerisation, adopt three sections to heat up 170 ℃-180 ℃, 220 ℃-230 ℃, 290-300 ℃ of polymerization technique polymerization obtains the ammonium polyphosphate particle, adopt the urethane coating material that modification is carried out on the ammonium polyphosphate surface again, obtain particle diameter and can reach 500 purpose electron triammonium polyphosphate fire retardants.
CN 200610008190 2006-02-27 2006-02-27 Production of electron triammonium polyphosphate fire retardant Pending CN101029235A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200610008190 CN101029235A (en) 2006-02-27 2006-02-27 Production of electron triammonium polyphosphate fire retardant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200610008190 CN101029235A (en) 2006-02-27 2006-02-27 Production of electron triammonium polyphosphate fire retardant

Publications (1)

Publication Number Publication Date
CN101029235A true CN101029235A (en) 2007-09-05

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CN 200610008190 Pending CN101029235A (en) 2006-02-27 2006-02-27 Production of electron triammonium polyphosphate fire retardant

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CN (1) CN101029235A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102229424A (en) * 2011-03-01 2011-11-02 濮阳市诚科化工科技有限公司 Ammonium polyphosphate grafting modification preparation method
CN102674287A (en) * 2012-04-28 2012-09-19 南通紫鑫实业有限公司 Method for producing ammonium polyphosphate flame retardant by utilizing melamine tail gas
CN104528682A (en) * 2014-12-18 2015-04-22 防城港博森化工有限公司 Method for preparing full water-soluble ammonium polyphosphate water solution by using wet process phosphoric acid
CN104962100A (en) * 2015-06-19 2015-10-07 南京林业大学 Method for manufacturing inflaming retarding straw-plastic composite materials through ammonium polyphosphate processed through cold plasma
CN105347323A (en) * 2015-12-15 2016-02-24 防城港博森化工科技股份有限公司 Method of preparing ammonium polyphosphate by using phosphoric acid by wet process and yellow phosphorus as raw materials
CN108383097A (en) * 2018-05-15 2018-08-10 佳瑞科(武汉)国际贸易有限公司 A method of utilizing extraction Wet-process Phosphoric Acid Production water solubility ammonium polyphosphate
CN108675275A (en) * 2018-05-28 2018-10-19 湖北工业大学 A method of utilizing the agricultural ammonium polyphosphate of Wet-process Phosphoric Acid Production

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102229424A (en) * 2011-03-01 2011-11-02 濮阳市诚科化工科技有限公司 Ammonium polyphosphate grafting modification preparation method
CN102229424B (en) * 2011-03-01 2012-06-27 濮阳市诚科化工科技有限公司 Ammonium polyphosphate grafting modification preparation method
CN102674287A (en) * 2012-04-28 2012-09-19 南通紫鑫实业有限公司 Method for producing ammonium polyphosphate flame retardant by utilizing melamine tail gas
CN104528682A (en) * 2014-12-18 2015-04-22 防城港博森化工有限公司 Method for preparing full water-soluble ammonium polyphosphate water solution by using wet process phosphoric acid
CN104962100A (en) * 2015-06-19 2015-10-07 南京林业大学 Method for manufacturing inflaming retarding straw-plastic composite materials through ammonium polyphosphate processed through cold plasma
CN104962100B (en) * 2015-06-19 2017-05-17 南京林业大学 Method for manufacturing inflaming retarding straw-plastic composite materials through ammonium polyphosphate processed through cold plasma
CN105347323A (en) * 2015-12-15 2016-02-24 防城港博森化工科技股份有限公司 Method of preparing ammonium polyphosphate by using phosphoric acid by wet process and yellow phosphorus as raw materials
CN108383097A (en) * 2018-05-15 2018-08-10 佳瑞科(武汉)国际贸易有限公司 A method of utilizing extraction Wet-process Phosphoric Acid Production water solubility ammonium polyphosphate
CN108675275A (en) * 2018-05-28 2018-10-19 湖北工业大学 A method of utilizing the agricultural ammonium polyphosphate of Wet-process Phosphoric Acid Production
CN108675275B (en) * 2018-05-28 2019-11-08 湖北工业大学 A method of utilizing the agricultural ammonium polyphosphate of Wet-process Phosphoric Acid Production

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