CN1490137A - Nonconsumable wood flame retardant and its preparation - Google Patents
Nonconsumable wood flame retardant and its preparation Download PDFInfo
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- CN1490137A CN1490137A CNA021311714A CN02131171A CN1490137A CN 1490137 A CN1490137 A CN 1490137A CN A021311714 A CNA021311714 A CN A021311714A CN 02131171 A CN02131171 A CN 02131171A CN 1490137 A CN1490137 A CN 1490137A
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- urea
- phosphoric acid
- fire retardant
- ammoniacal liquor
- formaldehyde
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- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
An anti-losing flame-retarding agent for wood or other organic fibre materials is prepared from formaldehyde, urea, ammonia water, phosphoric acid, cyanuramide and/or guanidine phosphate and/or guanidine sulfate, and polyethanediol and/or pentacrythrite and/or dextrin.
Description
Technical field
The present invention relates to a kind of fire retardant, particularly a kind of timber and fire-retardant phosphorus-nitrogen of other organic fibrous material of being applicable to is the high molecular fire retardant resin of anti-current mistake type.The invention still further relates to the preparation method of this fire retardant.
Background technology
Timber is that the important raw and processed materials and the people's lives of nation-building must articles for use.Because it is inflammable, timber from ancient times to the present is to cause fire and make one of arch-criminal of fire spread expansion, therefore, timber is carried out the effective measures that flame treatment has become fire-fighting fire-proof.
Wood fire retardant commonly used has the ammonium phosphate, ammonium dihydrogen phosphate (ADP), diammonium hydrogen phosphate, APP, dicyandiamide, melamine of phosphorus-nitrogen system etc.; The borax of boron system, boric acid, Firebrake ZB, ammonium pentaborate etc.; Ammonium halide such as ammonium chloride, ammonium bromide and the chlorinated paraffin wax etc. of halogen system; The hydrated alumina of inorganic oxide and oxygen hydrogenation system, magnesium hydroxide, antimony oxide etc.; In addition can also be with some other ammonium salts such as ammonium carbonate, ammonium sulfate and sodium metasilicate (waterglass) as wood fire retardant.Two not the fire retardant of homology can produce synergy sometimes, improve flame retardant effect, the normal fire retardant that adopts two or more mixes and uses in therefore using.
Above-mentioned fire retardant major part is a water-soluble substances.Water-insoluble fire retardant such as hydrated alumina, magnesium hydroxide, antimony oxide etc. are originally as nontransparent powdery solid, and because of being difficult to infiltrate through timber inside, it is fire-retardant generally only to be applied to surface applied.Adopting the fire retardant aqueous solution to impregnate and handling is that timber or other fibrous material are the most frequently used methods, and it has kept the decorative appearance and the physical and mechanical property of material basically.APP is the method for impregnating a kind of fire retardant with the most use, it is the same with other water-soluble flame retardant all to exist the easy moisture absorption, not water-fast shortcoming, make the serviceability of material be subjected to very big influence, as causing the surface of fire retarding wood to paint degradation, phenomenons such as coating whiting, foaming, resistance to ag(e)ing difference appear easily.Behind these water-soluble flame retardants of wood impregnation, major part can be drawn intensity and be descended, and generally descends about 5～10% in addition.
Publication number is that the patent application of CN1075673A has disclosed a kind of organic and inorganic mixed type, adopt the aqueous solution such as APP, diammonium hydrogen phosphate, phosphorus trichloride, three toraks, colloidal antimony, tetrabromobisphenol A, sodium metasilicate and phosphoric acid, after high temperature high pressure process, make the fire retardant that wood impregnation is used, has flame retardant effect preferably, but do not consider to handle the moisture absorption and the intensity decline problem of back timber, and will use the high pressure manufacturing equipment; Publication number is that the patent application of CN1126234A discloses a kind of wood fire retardant: adopt urea, phosphoric acid, borax, formaldehyde, aluminium salt and non-ionic surface active agent to make a kind of paste product, as flame-retardant additive, mix the back with the raw material of wood-based plate such as particieboard and use.This paste product is because viscosity is big, water-soluble bad, be difficult to as impregnating fire retardant: publication number is that the patent application of CN1030110A has proposed a kind of fire retardant for paper: a component is through the phosphoric acid of 130 ℃ of reactions, urea liquid, mixes the back with another component formaldehyde, the melamine solution handled at 40～70 ℃ and uses.This fire retardant is from its synthesis technique, if be used for treating of wood, and might be too high, acid content is excessive causes that the timber burst size of methanal exceeds standard, wooden perishable change owing to free aldehyde.
Summary of the invention
One of the object of the invention provides a kind of timber or other organic fibrous material with anti-current mistake type fire retardant, and this fire retardant normal temperature or heat drying solidify, and become water-fast transparent vitreous body high polymer after the curing.Timber or other organic fibrous material after this fire retardant is handled, when having desirable flame retardant effect, fire retardant moisture absorption problem has obtained solution, and material has anti-corrosive properties, and mechanical property such as intensity, hardness etc. also are improved.Another object of the present invention provides the synthetic method of this fire retardant.
Concrete technical scheme is as follows:
Nonconsumable wood flame retardant prescription of the present invention is (W/W):
Formaldehyde 〉=35%, technical grade 20.5～26.5
Ammoniacal liquor 〉=25%, technical grade 4
Urea 〉=98%, technical grade 4.3～5.0
Phosphoric acid 〉=85%, technical grade 0.5
Blowing agent technical grade 4～10
Carbon forming agent technical grade 9～20
Water running water 20
Synthetic method is: in formaldehyde, ammoniacal liquor, most of urea and the reaction of blowing agent input, be warming up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid, be incubated 30min again, add carbon forming agent, adjust pH value to 5.0 with phosphoric acid or ammoniacal liquor behind the stirring 20min, add entry and remaining urea continues to stir, discharging is fire retardant of the present invention after 40～50 ℃ of the temperature.
Nonconsumable wood flame retardant is synthetic by formaldehyde, urea, ammoniacal liquor, phosphoric acid, blowing agent and carbon forming agent.Wherein blowing agent is selected melamine and/or phosphoguanidine and/or guanidine sulfate.Blowing agent is met fire can decompose and discharge non-flammable gases such as nitrogen, steam, carbon dioxide, with other composition of the fire retardant that reaches softening point, effusion wood surface and foaming and intumescing form cavernous body three-D space structure secluding air and fire-retardant: carbon forming agent adopts polyethylene glycol and/or pentaerythrite and/or dextrin.Carbon forming agent is the basis of formation spongelike structure charring layer under the fire retardant high temperature, and charring layer is played skeleton function.
Synthetic fire retardant is a kind of low viscosity resin.Urea, blowing agent become the long-chain macromolecule with the aldehyde radical condensation reaction in building-up process, after impregnating timber or other organic fibrous material, in the dry run along with the volatilization of moisture, the reduction of pH, other composition crosslinked and fire retardant takes place and is solidified into water-insoluble solid together in these long-chain macromolecules.
In the composition of raw materials of Nonconsumable wood flame retardant of the present invention, though the mol ratio of formaldehyde-urea is bigger, but because blowing agent also can carry out condensation reaction with formaldehyde, in fact the molal quantity of formaldehyde is little of about 1.2 with the ratio of the molal quantity of (urea+blowing agent), and carbon forming agent is a polyol, higher with the aldehyde radical reactivity, it is effective, commonly used free aldehyde agent for capturing, therefore, the present invention synthetic the content of free aldehyde of fire retardant≤0.1%, low more than 10 times than national compulsory operative norm (≤1.0%).The free aldehyde burst size of timber after the flame treatment is≤0.1mg/L that than low 15 times of state compulsory standard one class plate (≤1.5mg/L allows exposed the use), two class plates (≤5.0mg/L allows the japanning back to use) are low more than 50 times.
Nonconsumable wood flame retardant of the present invention, immersing wood or when directly spraying, brushing other organic fibrous material and carrying out flame treatment, normal temperature or heat drying solidify all can.
The specific embodiment
In order to understand better, further set forth the present invention below in conjunction with embodiment, but these embodiment should not be construed as any limitation of the invention.
Embodiment 1:
Formaldehyde 21.0Kg, ammoniacal liquor 4Kg, urea 4.0Kg and melamine 8.0Kg are dropped in the reactor, be warming up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5Kg, be incubated 30min again, add polyethylene glycol 12.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.3Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 2:
Formaldehyde 23.0Kg, ammoniacal liquor 4Kg, urea 3.8Kg and melamine 10.0Kg are dropped in the reactor, be warming up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5Kg, be incubated 30min again, add pentaerythrite 11.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.4Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 3:
Formaldehyde 26.5Kg, ammoniacal liquor 4Kg, urea 4.1Kg and melamine 4.5Kg are dropped in the reactor, be warmed up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5mKg, be incubated 30min again, add dextrin 9.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.8Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 4:
Formaldehyde 20.5Kg, ammoniacal liquor 4Kg, urea 4.5Kg and phosphoguanidine 4.5Kg are dropped in the reactor, be warmed up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5mKg and be incubated 30min again, add pentaerythrite 9.0Kg, behind the stirring 20min, adjust material pH value to 5.0 with phosphoric acid or ammoniacal liquor, add entry 20Kg and urea 0.5Kg and continue to stir, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 5
Formaldehyde 24.5Kg, ammoniacal liquor 4Kg, urea 4.2Kg and phosphoguanidine 6.5Kg are dropped in the reactor, be warmed up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5mKg, be incubated 30min again, add polyethylene glycol 20.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.8Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 6
Formaldehyde 22.0Kg, ammoniacal liquor 4Kg, urea 4.4Kg and phosphoguanidine 8.5Kg are dropped in the reactor, be warmed up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5mKg, be incubated 30min again, add dextrin 14.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.5Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 7:
Formaldehyde 22.5Kg, ammoniacal liquor 4Kg, urea 4.0Kg and phosphoguanidine 4.0Kg are dropped in the reactor, be warmed up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5mKg, be incubated 30min again, add dextrin 10.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.3Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 8:
Formaldehyde 23.0Kg, ammoniacal liquor 4Kg, urea 4.2Kg and phosphoguanidine 4.5Kg are dropped in the reactor, be warmed up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5mKg, be incubated 30min again, add pentaerythrite 15.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.3Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Embodiment 9:
Formaldehyde 26.5Kg, ammoniacal liquor 4Kg, urea 4.5Kg and guanidine sulfate 5.0Kg are dropped in the reactor, be warmed up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid～0.5mKg, be incubated 30min again, add polyethylene glycol 18.0Kg, after stirring 20min, adjust material pH value to 5.0, add entry 20Kg and urea 0.5Kg and continue to stir with phosphoric acid or ammoniacal liquor, discharging after 40～50 ℃ of the temperature is Nonconsumable wood flame retardant of the present invention.
Because fire retardant of the present invention is a kind of curable macromolecule resin, impregnate processing dried timber or other organic fibrous material through this fire retardant, have good resistance to water and corrosion resistance, intensity, hardness are improved, and the original outward appearance (as wood grain, color etc.) of material does not have significant change.Detect its anti-flammability by CA/T42.1-92 (adopting Unite States Standard ASTME160), rate of lostmass after fire is 28～50%, and it is 2.25～3.5min that the flame combustion cymbals time is arranged, and reaches the standard of fire retarding wood.
The performance indications of fire retardant of the present invention are as follows:
Appearance colorless is transparent
Viscosity/be coated with-4 glass, S 13～30
PH value 5.0～6.0
Solid content/% 25.0～31.5
Free aldehyde/%≤0.1
Claims (5)
1, a kind of Nonconsumable wood flame retardant, synthetic by formaldehyde, urea, ammoniacal liquor, phosphoric acid, blowing agent and carbon forming agent, it is characterized in that prescription is (W/W):
Formaldehyde 〉=35%, technical grade 20.5～26.5
Ammoniacal liquor 〉=25%, technical grade 4
Urea 〉=98%, technical grade 4.3～5.0
Phosphoric acid 〉=85%, technical grade 0.5
Blowing agent technical grade 4～10
Carbon forming agent technical grade 9～20
Water running water 20
2, fire retardant as claimed in claim 1 is characterized in that described blowing agent is one or more in melamine, phosphoguanidine and the guanidine sulfate.
3, fire retardant as claimed in claim 1 is characterized in that described carbon forming agent is one or more in polyethylene glycol, pentaerythrite and the dextrin.
4, a kind of method for preparing claim 1 fire retardant, it is characterized in that: in formaldehyde, ammoniacal liquor, most of urea and the reaction of blowing agent input, be warming up to 80～90 ℃ of insulation 30～60min, be cooled to 60～70 ℃, add phosphoric acid, be incubated 30min again, add carbon forming agent, adjust pH value to 5.0 with phosphoric acid or ammoniacal liquor after stirring 20min, add entry and remaining urea continues stirring, discharging after 40～50 ℃ of the temperature.
5, method as claimed in claim 4 is characterized in that described fire retardant content of free aldehyde≤0.1%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021311714A CN1304183C (en) | 2002-10-15 | 2002-10-15 | Nonconsumable wood flame retardant and its preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021311714A CN1304183C (en) | 2002-10-15 | 2002-10-15 | Nonconsumable wood flame retardant and its preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1490137A true CN1490137A (en) | 2004-04-21 |
| CN1304183C CN1304183C (en) | 2007-03-14 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB021311714A Expired - Fee Related CN1304183C (en) | 2002-10-15 | 2002-10-15 | Nonconsumable wood flame retardant and its preparation |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101052662B (en) * | 2005-09-01 | 2011-09-21 | 天然纤维与药用植物研究所 | Expansion fire retardant agent and its manufacture |
| CN101121892B (en) * | 2006-08-09 | 2011-10-05 | 上海高技企业发展公司 | Expansion type flame-retardant and its preparation method |
| CN101508898B (en) * | 2009-03-17 | 2012-06-06 | 公安部四川消防研究所 | Flame-proof liquid special for historic building and method of preparing the same |
| CN103862541A (en) * | 2014-03-27 | 2014-06-18 | 马新闻 | Resin type wood fire retardant, preparation method thereof and manufacturing method of laminated veneer lumber containing resin type wood fire retardant |
| CN105102193A (en) * | 2013-02-15 | 2015-11-25 | 汉莎航空技术股份公司 | Flame-retardant wooden substrate |
| CN105859915A (en) * | 2016-06-12 | 2016-08-17 | 沈阳化工大学 | Preparation method of environment-friendly biobase three-source-integrated fire retardant |
| CN106574187A (en) * | 2014-06-13 | 2017-04-19 | Csir公司 | Liquid flame retardant composition |
| CN108247795A (en) * | 2017-11-29 | 2018-07-06 | 浙江金三蝶板业有限公司 | A kind of production method of the mould proof solid wooden compound floor of flame-proof antibiotic |
| CN113910390A (en) * | 2021-10-22 | 2022-01-11 | 安徽梵齐诺拒火材料开发有限公司 | Fire-resisting agent for wood |
| CN114008821A (en) * | 2019-06-28 | 2022-02-01 | 日本瑞翁株式会社 | Composite particle for electrochemical element and method for producing same, binder composition for electrochemical element functional layer and method for producing same, conductive material paste for electrode composite layer and method for producing same, slurry for electrode composite layer, electrode for electrochemical element, and electrochemical element |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5010113A (en) * | 1989-06-01 | 1991-04-23 | Blount David H | Flame-retardant polyurethane products |
| HU204713B (en) * | 1989-06-30 | 1992-02-28 | Erdoekemia Erdoegazdasagi | Method for producing composition serving for making anti-flame wood and structural materials made of wood |
| JPH1148503A (en) * | 1997-08-05 | 1999-02-23 | Seiko Epson Corp | Ink-jet recording head and ink-jet recording apparatus |
-
2002
- 2002-10-15 CN CNB021311714A patent/CN1304183C/en not_active Expired - Fee Related
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101052662B (en) * | 2005-09-01 | 2011-09-21 | 天然纤维与药用植物研究所 | Expansion fire retardant agent and its manufacture |
| CN101121892B (en) * | 2006-08-09 | 2011-10-05 | 上海高技企业发展公司 | Expansion type flame-retardant and its preparation method |
| CN101508898B (en) * | 2009-03-17 | 2012-06-06 | 公安部四川消防研究所 | Flame-proof liquid special for historic building and method of preparing the same |
| CN105102193A (en) * | 2013-02-15 | 2015-11-25 | 汉莎航空技术股份公司 | Flame-retardant wooden substrate |
| CN103862541A (en) * | 2014-03-27 | 2014-06-18 | 马新闻 | Resin type wood fire retardant, preparation method thereof and manufacturing method of laminated veneer lumber containing resin type wood fire retardant |
| CN106574187A (en) * | 2014-06-13 | 2017-04-19 | Csir公司 | Liquid flame retardant composition |
| CN105859915A (en) * | 2016-06-12 | 2016-08-17 | 沈阳化工大学 | Preparation method of environment-friendly biobase three-source-integrated fire retardant |
| CN105859915B (en) * | 2016-06-12 | 2018-04-27 | 沈阳化工大学 | A kind of preparation method of environment-friendly and bio base " three-source integrated " fire retardant |
| CN108247795A (en) * | 2017-11-29 | 2018-07-06 | 浙江金三蝶板业有限公司 | A kind of production method of the mould proof solid wooden compound floor of flame-proof antibiotic |
| CN114008821A (en) * | 2019-06-28 | 2022-02-01 | 日本瑞翁株式会社 | Composite particle for electrochemical element and method for producing same, binder composition for electrochemical element functional layer and method for producing same, conductive material paste for electrode composite layer and method for producing same, slurry for electrode composite layer, electrode for electrochemical element, and electrochemical element |
| CN113910390A (en) * | 2021-10-22 | 2022-01-11 | 安徽梵齐诺拒火材料开发有限公司 | Fire-resisting agent for wood |
Also Published As
| Publication number | Publication date |
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| CN1304183C (en) | 2007-03-14 |
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