CN104558685A - Phosphorus-nitrogen intumescent flame retardant and synthesis method thereof - Google Patents
Phosphorus-nitrogen intumescent flame retardant and synthesis method thereof Download PDFInfo
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- CN104558685A CN104558685A CN201310506631.6A CN201310506631A CN104558685A CN 104558685 A CN104558685 A CN 104558685A CN 201310506631 A CN201310506631 A CN 201310506631A CN 104558685 A CN104558685 A CN 104558685A
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Abstract
The invention relates to a phosphorus-nitrogen intumescent flame retardant and a synthesis method thereof. The synthesis method comprises the steps: mixing neopentyl glycol and a solvent, adding a catalyst, dissolving the catalyst, then, adding phosphorus oxychloride into a reaction solution under the condition of stirring at the temperature of 0-10 DEG C, reacting for 4-8 hours at the temperature of 20-50 DEG C after phosphorus oxychloride is added completely, removing the solvent through distilling after reacting ends, and washing and drying residues, so as to obtain cyclic phosphoryl chloride; adding the obtained cyclic phosphoryl chloride and an acid binding agent into a solvent, stirring to dissolve, adding diamine into a reaction solution under the condition of stirring at the temperature of 15-30 DEG C, then, reacting for 8-12 hours at the temperature of 50-110 DEG C, removing the solvent through distilling after reacting ends, and washing and drying residues, thereby obtaining the phosphorus-nitrogen intumescent flame retardant. The phosphorus-nitrogen intumescent flame retardant and the synthesis method thereof have the advantages that the synthesis process is simple, the reaction time is short, the product has a melting point, the transparency is good when the flame retardant is added into materials, the flame-retardant effect is good, the influence on mechanical properties is low, and the like; and meanwhile, the disadvantage that intumescent flame retardants cannot be applied to the flame retardance of engineering plastics due to poor thermal stability is overcome.
Description
Technical field
The invention belongs to organic chemistry filed, be specifically related to a kind of phosphorous-nitrogen combustion inhibitor and synthetic method thereof.
Background technology
Since the 80's of 20th century, fire retardant has become one of most important auxiliary agent of macromolecular material, and its consumption also increases increasingly.In numerous fire retardant, organophosphorous fire retardant because having environmental friendliness and the feature such as efficient, and is acknowledged as and can replaces the important kind of halogenated flame retardant.It, while giving the good flame retardant resistance of material, compared with halogenated flame retardant, has raw smoke which few, not easily forms the features such as poisonous and corrosive gases.In recent years, the work studying organophosphorous fire retardant has become the heat subject of flame retardant area.
The halogen-free flame retardants that phosphorous expanding fire retardant is is main component with phosphorus, nitrogen, when with the addition of the superpolymer heated combustion of this based flame retardant, surface energy generates the uniform carbonaceous foam layer of one deck, this layer of charcoal has heat insulation, oxygen barrier at condensed phase, presses down cigarette and prevent the effect of molten drop thus reach flame retardant effect, has good resistivity to long-time or repeated exposure in flame.It not only has excellent expandable flame retardant effect, and it is large to overcome other fire retardant combustion fumes, the shortcoming of many molten drops and inorganics fire retardant, because addition is greatly to the detrimentally affect that the mechanics of materials, processibility the subject of knowledge and the object of knowledge bring, become one of flame retardant area enlivened the most in recent years.
Individually disclose in US Patent No. 4544695 A and Chinese patent CN101225310 A a kind of phosphorous-synthetic method of nitrogen expanding fire retardant, and for improvement of the flame retardant properties of acrylic plastering.CN 102093566 A discloses and adopts volution phosphoryl chloride and DAP to be raw material, poly-chloro-2,4,8,10-tetra-oxo-3,9-hosphospiro-3,9-dioxy [5,5] the undecane DAP fire retardants of 3,9-bis-of synthesis.The poly-volution phosphinylidyne amine type expanding fire retardant that patent CN 102352041 A is synthesized by three-step approach, can be applicable to PP flame retardant of plastic.
In addition, also have some about the report of phosphorus-nitrogen combustion inhibitor synthesis, as patent WO 2012071732 A1 also discloses a kind of preparation of polymer-type P-N expanding fire retardant, also have patent CN 102417596 A; CN 1379078 A; CN 1824731 A; CN 1891706 A; H. Y. Ma etc. (Polym. Degrad. Stab. 2007,92:720-726); J. D. Zuo etc. (Moleculars. 2010,15:7593-7602); Y. Tang etc. (J. Appl. Polym. Sci. 2008,108:1216-1222).But the fire retardant of phosphorus-nitrogen systems that these patents and document are reported all comes with some shortcomings, mainly product is liquid, low melting point solid or without melting point solid, be not easy to processing, thermostability is not high, after interpolation, the mechanical properties decrease of material is comparatively large, cannot be applied to the fire-retardant of engineering plastics, thus range of application is limited by very large, to the flame retardant effect of engineering plastics and and the compatibility of material also need further raising.
summary of the invention:
The present invention is directed to existing phosphorus-nitrogen combustion inhibitor thermostability not high, large to the Effect on Mechanical Properties of material after interpolation, the shortcoming cannot applied in engineering plastics, proposes a kind of phosphorus nitrogen expansion type combustion inhibitor and synthetic method thereof.Phosphorus nitrogen expansion type combustion inhibitor of the present invention has high, the easy processing of thermostability, excellent flame retardancy and affects little advantage to material mechanical performance.And synthetic method of the present invention is simple, the reaction times is short, reaction solvent recoverable pollutes little.
The invention provides a kind of phosphorus nitrogen expansion type combustion inhibitor, molecular structural formula as shown in the formula (I):
formula (I)
In formula (I), X is
,
,
in any one.
The synthetic method step of above-mentioned phosphorus nitrogen expansion type combustion inhibitor provided by the invention is as follows:
(1) by neopentyl glycol and solvent, and add catalyzer, neopentyl glycol is made to be dissolved in completely in solvent under agitation, phosphorus oxychloride is added in 0 ~ 10 DEG C of agitation condition downhill reaction liquid, at 20 ~ 50 DEG C, 4 ~ 8h is reacted after phosphorus oxychloride adds, remove desolventizing by distillation after reaction terminates, resistates obtains ring-type phosphoryl chloride after washing drying;
(2) step (1) gained ring-type phosphoryl chloride, acid binding agent are joined stirring and dissolving in solvent, diamine compound is added in 15 ~ 30 DEG C of agitation condition downhill reaction liquid, at 50 ~ 110 DEG C, 8 ~ 12h is reacted after diamine compound adds, remove desolventizing by distillation after reaction terminates, resistates obtains phosphorus nitrogen expansion type combustion inhibitor after washing drying.
In the inventive method, in step (1), neopentyl glycol and solvent quality are than being 1:4 ~ 1:18, preferred 1:6 ~ 1:10, neopentyl glycol and phosphorus oxychloride mol ratio are 1:1 ~ 1:4, preferred 1:1 ~ 1:2, described catalyst levels is 2% ~ 20% of neopentyl glycol weight, preferably 6% ~ 15%.
In the inventive method, in step (2), ring-type phosphoryl chloride and solvent quality are than being 1:8 ~ 1:25, preferred 1:9 ~ 1:18, ring-type phosphoryl chloride and diamine compounds mole are 2:1 ~ 5:1, preferred 2:1 ~ 3:1, described acid binding agent consumption is 2% ~ 20% of ring-type phosphoryl chloride weight, preferably 5% ~ 16%.
Solvent described in the inventive method is one or more in chloroform, tetracol phenixin, acetonitrile, tetrahydrofuran (THF), toluene and dimethylbenzene, is preferably chloroform.
In the inventive method step (1), used catalyst is one or more in triethylamine, quadrol, pyridine, piperidines, N, N-diisopropyl ethyl amine, Aluminum chloride anhydrous and Magnesium Chloride Anhydrous, is preferably Aluminum chloride anhydrous and/or Magnesium Chloride Anhydrous.
In the inventive method diamine compounds described in step (2) can be between ring pentamethylene diamine, methyl ring pentamethylene diamine, any one in adjacent diamines methylcyclopentane.
In the inventive method step (2), acid binding agent used is triethylamine, quadrol, pyridine, piperidines, N, one or more in N-diisopropyl ethyl amine, Aluminum chloride anhydrous, Magnesium Chloride Anhydrous, alkali metal hydroxide, alkaline carbonate and alkali metal hydrocarbonate, preferred Aluminum chloride anhydrous or Magnesium Chloride Anhydrous, wherein alkali metal hydroxide can be NaOH and/or KOH, and alkaline carbonate is Na
2cO
3and/or K
2cO
3, alkali metal hydrocarbonate is NaHCO
3and/or KHCO
3.
Distillation described in the inventive method is underpressure distillation.
Washing described in the inventive method is for using deionized water wash 1 ~ 5 time.
Drying described in the inventive method is vacuum-drying 8 ~ 12 hours at 40 ~ 60 DEG C.
Synthetic route of the present invention is as follows:
Product of the present invention joins in polycarbonate as flame-retardant additive, transparent fire-retardant sample can be obtained, when addition is 5-8wt%, by UL94 V0 level, in addition, product of the present invention can also be applied to the fire-retardant of poly-paraphenylene terephthalamide's glycol ester, poly-paraphenylene terephthalamide's butanediol ester and the engineering plastics such as acrylonitrile-butadiene-styrene ternary copolymerized.
Phosphorus nitrogen expansion type combustion inhibitor of the present invention is the expanding fire retardant of collection acid source, source of the gas and carbon source three-in-one, as the flame-retardant additive of engineering plastics, polyphosphoric acid and tetra-sodium class material can be generated during burning, promote that material becomes charcoal, form fire-retardant foamed char, cover material surface, stop it to burn further.Product of the present invention is white powder, and productive rate is more than 80%, and 5% heat decomposition temperature is more than 280 DEG C.Product melting when heating, reduce foaming expansion, and the final foamed char generating good strength, has good one-tenth charcoal and swelling capacity, and the advantage of Heat stability is good.
Synthesis technique of the present invention is simple, reaction times is short, and product has fusing point, add transparency in material to good, as compared to existing BDP with the RDP fire retardant for engineering plastics, there is easy processing, good flame retardation effect, the advantages such as Effect on Mechanical Properties is little, overcome expanding fire retardant poor heat stability simultaneously and cannot be applied to the fire-retardant shortcoming of engineering plastics.
Embodiment
Further illustrate phosphorus nitrogen expansion type combustion inhibitor preparation method of the present invention below by embodiment, these embodiments only for illustration of the present invention, and do not limit the present invention.
Embodiment 1
83.2g neopentyl glycol and 500mL acetonitrile is added in the 2000mL four-hole bottle that reflux exchanger, thermometer, agitator, constant pressure funnel are housed, then 8g aluminum trichloride (anhydrous) is added, abundant stirring makes material dissolution, then four-hole bottle is put into ice-water bath, under 5 DEG C of agitation conditions, by 128.8g phosphorus oxychloride by slowly joining in four-hole boiling flask in constant pressure funnel, temperature of reaction controls at 0 ~ 10 DEG C, time for adding is 2h, after phosphorus oxychloride dropwises, temperature is risen to 50 DEG C, and react 6h at this temperature.After reaction terminates, by vacuum distillation recovered solvent, residual solid deionized water wash 2 times, and 60 DEG C of vacuum-dryings 10 hours, obtain 136.1g ring-type phosphoryl chloride, 2-chloro-2-oxo-5,5-dimethyl-1,3,2-dioxaphosphorinane, productive rate 92.3wt%.
In the 2000mL four-hole bottle that reflux exchanger, thermometer, agitator, constant pressure funnel are housed, add 74g ring-type phosphoryl chloride, 8g pyridine and 800mL tetrahydrofuran (THF), make it fully dissolve under agitation.Under 10 DEG C of agitation conditions, by 20.0g 1,3 ring pentamethylene diamines add in four-hole boiling flask, after treating that ring pentamethylene diamine adds, temperature are risen to 60 DEG C, and react 12h at this temperature, by vacuum distillation recovered solvent after reaction terminates, resistates deionized water wash 3 times, obtains white solid powder, product 67.5g is obtained, productive rate 91.7wt% after 60 DEG C of dry 10h.Product fusing point 120.5 ~ 120.9 DEG C.The test analysis of TGA shows, the thermal weight loss decomposition temperature of this product 5% is 298.6 DEG C.
The structural formula of the product obtained in present embodiment is as follows:
Embodiment 2
83.2g neopentyl glycol and 500mL tetracol phenixin is added in the 2000mL four-hole bottle that reflux exchanger, thermometer, agitator, constant pressure funnel are housed, then 8g aluminum trichloride (anhydrous) is added, abundant stirring makes material dissolution, then four-hole bottle is put into ice-water bath, under 5 DEG C of agitation conditions, by 128.8g phosphorus oxychloride by slowly joining in four-hole boiling flask in constant pressure funnel, temperature of reaction controls at 0 ~ 10 DEG C, time for adding is 2h, after phosphorus oxychloride dropwises, temperature is risen to 50 DEG C, and react 6h at this temperature.After reaction terminates, by vacuum distillation recovered solvent, residual solid deionized water wash 2 times, and 60 DEG C of vacuum-dryings 10 hours, obtain 135.0g ring-type phosphoryl chloride, 2-chloro-2-oxo-5,5-dimethyl-1,3,2-dioxaphosphorinane, productive rate 91.5wt%.
In the 2000mL four-hole bottle that reflux exchanger, thermometer, agitator, constant pressure funnel are housed, add 74g ring-type phosphoryl chloride, 8g aluminum trichloride (anhydrous) and 800mL tetrahydrofuran (THF), make it fully dissolve under agitation.Under 10 DEG C of agitation conditions, adjacent for 22.4g diamines methylcyclopentane is added in four-hole boiling flask, after treating that adjacent diamines methylcyclopentane adds, temperature is risen to 60 DEG C, and react 12h at this temperature, after reaction terminates, pass through vacuum distillation recovered solvent, resistates deionized water wash 3 times, obtain white solid powder, after 60 DEG C of dry 10h, obtain product 75.5g, productive rate 92.3wt%.Product fusing point 121.9 ~ 122.4 DEG C.The test analysis of TGA shows, the thermal weight loss decomposition temperature of this product 5% is 300.5 DEG C.
The structural formula of the product obtained in present embodiment is as follows:
Embodiment 3
83.2g neopentyl glycol and 500mL chloroform is added in the 2000mL four-hole bottle that reflux exchanger, thermometer, agitator, constant pressure funnel are housed, then 8g Magnesium Chloride Anhydrous is added, abundant stirring makes material dissolution, then four-hole bottle is put into ice-water bath, under 5 DEG C of agitation conditions, by 128.8g phosphorus oxychloride by slowly joining in four-hole boiling flask in constant pressure funnel, temperature of reaction controls at 0 ~ 10 DEG C, time for adding is 2h, after phosphorus oxychloride dropwises, temperature is risen to 50 DEG C, and react 6h at this temperature.After reaction terminates, by vacuum distillation recovered solvent, residual solid deionized water wash 2 times, and 60 DEG C of vacuum-dryings 10 hours, obtain 137.9g ring-type phosphoryl chloride, 2-chloro-2-oxo-5,5-dimethyl-1,3,2-dioxaphosphorinane, productive rate 93.5wt%.
In the 2000mL four-hole bottle that reflux exchanger, thermometer, agitator, constant pressure funnel are housed, add 74g ring-type phosphoryl chloride, 8g Magnesium Chloride Anhydrous and 800mL tetrahydrofuran (THF), make it fully dissolve under agitation.Under 10 DEG C of agitation conditions, 22.4g methyl ring pentamethylene diamine is added in four-hole boiling flask, after treating that methyl ring pentamethylene diamine adds, temperature is risen to 60 DEG C, and react 12h at this temperature, after reaction terminates, pass through vacuum distillation recovered solvent, resistates deionized water wash 3 times, obtain white solid powder, after 60 DEG C of dry 10h, obtain product 75.9g, productive rate 92.8 wt%.Product fusing point 119.2 ~ 120.1 DEG C.The test analysis of TGA shows, the thermal weight loss decomposition temperature of this product 5% is 303.8 DEG C.
The structural formula of the product obtained in present embodiment is as follows:
Embodiment 4
The present embodiment catalyzer used in step one and step 2 is 8.5g and 10.5g piperidines, and other is identical with embodiment 1.The product ring-type phosphoryl chloride obtained in step one is 137.0g, productive rate 92.9%, and obtaining product in step 2 is 67.3g, productive rate 91.4 wt%.
Embodiment 5
Present embodiment catalyzer used in step one and step 2 is respectively 8g and 9g triethylamine, and other is identical with embodiment 1.The product ring-type phosphoryl chloride obtained in step one is 132.9g, productive rate 90.1%, and obtaining product in step 2 is 66.8g, productive rate 90.8wt%.
Embodiment 6
Present embodiment catalyzer used in step one and step 2 is respectively 7.5g and 8.5g quadrol, and other is identical with embodiment 1.The product ring-type phosphoryl chloride obtained in step one is 131.7g, productive rate 89.3%, and obtaining product in step 2 is 65.1g, productive rate 88.4wt%.
Embodiment 7
Present embodiment catalyzer used in step one and step 2 is respectively 8g and 9g N, N-diisopropyl ethyl amine, and other is identical with embodiment 1.The product ring-type phosphoryl chloride obtained in step one is 131.4g, productive rate 89.1%, and obtaining product in step 2 is 65.4g, productive rate 88.9wt%.
Embodiment 8
Present embodiment catalyzer used in step 2 is the mixture of 9g sodium hydroxide, 25g water and 1.8g 4 bromide, and other is identical with embodiment 1.Obtaining product is 71.9g, productive rate 88.1wt%.
Embodiment 9
Present embodiment catalyzer used in step 2 is the mixture of 9g sodium bicarbonate, 25g water and 1.8g 4 bromide, and other is identical with embodiment 1.Obtaining product is 64.3g, productive rate 87.3wt%.
Embodiment 10
Present embodiment catalyzer used in step 2 is the mixture of 9g salt of wormwood, 25g water and 1.8g 4 bromide, and other is identical with embodiment 1.Obtaining product is 64.0g, productive rate 86.9wt%.
Embodiment 11
Present embodiment solvent used in step 2 is toluene, and temperature of reaction is 85 DEG C, and other is identical with embodiment 1.Obtaining product is 65.7g, productive rate 89.2wt%.
Embodiment 12
Present embodiment solvent used in step 2 is dimethylbenzene, and temperature of reaction is 85 DEG C, and other is identical with embodiment 1.Obtaining product is 65.5g, productive rate 89.0wt%.
Claims (17)
1. a phosphorus nitrogen expansion type combustion inhibitor, is characterized in that: described flame retardant molecule structural formula is:
formula (I)
In formula (I), X is
,
,
in any one.
2. a preparation method for phosphorus nitrogen expansion type combustion inhibitor according to claim 1, is characterized in that: comprise the steps:
(1) by neopentyl glycol and solvent, and add catalyzer, neopentyl glycol is made to be dissolved in completely in solvent under agitation, phosphorus oxychloride is added in 0 ~ 10 DEG C of agitation condition downhill reaction liquid, at 20 ~ 50 DEG C, 4 ~ 8h is reacted after phosphorus oxychloride adds, remove desolventizing by distillation after reaction terminates, resistates obtains ring-type phosphoryl chloride after washing drying;
(2) step (1) gained ring-type phosphoryl chloride, acid binding agent are joined stirring and dissolving in solvent, diamine compound is added in 15 ~ 30 DEG C of agitation condition downhill reaction liquid, at 50 ~ 110 DEG C, 8 ~ 12h is reacted after diamine compound adds, remove desolventizing by distillation after reaction terminates, resistates obtains phosphorus nitrogen expansion type combustion inhibitor after washing drying.
3. method according to claim 2, is characterized in that: in step (1), neopentyl glycol and solvent quality are than being 1:4 ~ 1:18, and neopentyl glycol and phosphorus oxychloride mol ratio are 1:1 ~ 1:4.
4. method according to claim 2, is characterized in that: in step (1), neopentyl glycol and solvent quality are than being 1:6 ~ 1:10, and neopentyl glycol and phosphorus oxychloride mol ratio are 1:1 ~ 1:2.
5. method according to claim 2, is characterized in that: in step (1), catalyst levels is 2% ~ 20% of neopentyl glycol weight.
6. method according to claim 2, is characterized in that: in step (1), catalyst levels is 6% ~ 15% of neopentyl glycol weight.
7. method according to claim 2, is characterized in that: in step (2), ring-type phosphoryl chloride and solvent quality are than being 1:8 ~ 1:25, and ring-type phosphoryl chloride and diamine compounds mole are 2:1 ~ 5:1.
8. method according to claim 2, is characterized in that: in step (2), ring-type phosphoryl chloride and solvent quality are than being 1:9 ~ 1:18, and ring-type phosphoryl chloride and diamine compounds mole are 2:1 ~ 3:1.
9. method according to claim 2, is characterized in that: in step (2), acid binding agent consumption is 2% ~ 20% of ring-type phosphoryl chloride weight.
10. method according to claim 2, is characterized in that: in step (2), acid binding agent consumption is 5% ~ 16% of ring-type phosphoryl chloride weight.
11. methods according to claim 2, is characterized in that: described solvent is one or more in chloroform, tetracol phenixin, acetonitrile, tetrahydrofuran (THF), toluene and dimethylbenzene.
12. methods according to claim 2, is characterized in that: described solvent is chloroform.
13. methods according to claim 2, is characterized in that: in step (1), used catalyst is one or more in triethylamine, quadrol, pyridine, piperidines, N, N-diisopropyl ethyl amine, Aluminum chloride anhydrous and Magnesium Chloride Anhydrous.
14. methods according to claim 2, is characterized in that: in step (1), used catalyst is Aluminum chloride anhydrous and/or Magnesium Chloride Anhydrous.
15. methods according to claim 2, is characterized in that: diamine compounds described in step (2) is any one in a ring pentamethylene diamine, methyl ring pentamethylene diamine, adjacent diamines methylcyclopentane.
16. methods according to claim 2, it is characterized in that: in step (2), acid binding agent used is one or more in triethylamine, quadrol, pyridine, piperidines, N, N-diisopropyl ethyl amine, Aluminum chloride anhydrous, Magnesium Chloride Anhydrous, alkali metal hydroxide, alkaline carbonate and alkali metal hydrocarbonate.
17. methods according to claim 2, is characterized in that: in step (2), acid binding agent used is Aluminum chloride anhydrous or Magnesium Chloride Anhydrous.
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| US11603523B2 (en) | 2019-01-18 | 2023-03-14 | Astrazeneca Ab | PCSK9 inhibitors and methods of use thereof |
Citations (1)
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| CN102352036A (en) * | 2011-06-16 | 2012-02-15 | 东北林业大学 | Triazine carbon forming-foaming agent, synthesis method of the triazine carbon forming-foaming agent, and flame-retardant polymer composite material prepared from the triazine carbon forming-foaming agent |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102352036A (en) * | 2011-06-16 | 2012-02-15 | 东北林业大学 | Triazine carbon forming-foaming agent, synthesis method of the triazine carbon forming-foaming agent, and flame-retardant polymer composite material prepared from the triazine carbon forming-foaming agent |
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|---|
| KOICHIRO MATSUMOTO ET AL.: "An Approach to a Chiral Cycloalkanone-Mediated Asymmetric Epoxidation of Stilbene with Oxone", 《CHEMICAL & PHARMACEUTICAL BULLETIN》 * |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US11603523B2 (en) | 2019-01-18 | 2023-03-14 | Astrazeneca Ab | PCSK9 inhibitors and methods of use thereof |
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