JP2008101179A - Flame retardant based on vegetable oil and fat - Google Patents

Flame retardant based on vegetable oil and fat Download PDF

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JP2008101179A
JP2008101179A JP2006312211A JP2006312211A JP2008101179A JP 2008101179 A JP2008101179 A JP 2008101179A JP 2006312211 A JP2006312211 A JP 2006312211A JP 2006312211 A JP2006312211 A JP 2006312211A JP 2008101179 A JP2008101179 A JP 2008101179A
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flame
parts
heat
vegetable oil
flame retardant
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Osamu Sugiyama
杉山  修
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HI VAN KK
HI-VAN KK
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HI-VAN KK
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a non-combustible, heat-resistant material that can be dried and molded at an ordinary temperature, using an environmentally friendly flame retardant based on a vegetable oil and fat, to also provide a fundamental technology for imparting flame retardance and heat resistance to a polymer material to which flame retardance has been imparted, and to further provide an ultra heat-resistant carbon superior to graphite by improving various characteristics including non-combustibility and ultra heat-resistance in a high-temperature oxidizing atmosphere by subjecting a material having been previously subjected to a flame-retardant treatment (material recycle) to thermal cracking, carbonization and firing. <P>SOLUTION: (1) The additive for imparting non-combustibility and flame-retardance to a material is prepared from a material comprising a soap material based on vegetable oil and fat containing lauric acid, water and a metal oxide inorganic filler. (2) The flame retardant comprises the soap material based on vegetable oil and fat containing lauric acid, PAC and the metal oxide inorganic filler. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

産業上の利用分野Industrial application fields

椰子油、パーム核油など植物油脂系をベースとした難燃性と環境保護の両立を目的とするものである。この難燃剤はエマルジョン系ポリマーに特に相溶性が優れている。
人、環境にとっても優しく且つ安価にその目的を達成することが可能である。
住宅火災が懸念される部位の内装用の壁、天井部位に簡易な方法で熱無溶融不燃性の芳香性塗膜も形成させることもできる。特に最近は高齢者を対象とした養護老人ホーム、一人暮らし高齢者に火災の恐怖がありそれらの危険部位に簡単に耐炎塗膜を施工する有効な方法を提供するものである。又、抗菌、除菌効果のある薬剤や脱臭剤をブレンドすることも可能です。
The objective is to achieve both flame retardancy and environmental protection based on vegetable oils such as coconut oil and palm kernel oil. This flame retardant is particularly compatible with emulsion polymers.
It is gentle to people and the environment, and it is possible to achieve its purpose at low cost.
It is also possible to form a heat non-melting and non-combustible aromatic coating film by a simple method on the interior wall or ceiling part where there is a concern about house fire. In particular, a nursing home for the elderly, and an elderly person living alone, who is afraid of fire, provides an effective method for easily applying a flame resistant coating to those dangerous areas. It is also possible to blend antibacterial and antibacterial agents and deodorizers.

水酸化アルミニュウム、水酸化マグネシュウム、硼酸、水ガラス系、りん酸系、塩化物などの無機難燃剤や有機りん酸エステル、ブロム化合物、グアニジン系などがその大勢を占め、植物由来の油脂系難燃剤は現在のところその知見はなく植物原料は微生物により分解される。Inorganic flame retardants such as aluminum hydroxide, magnesium hydroxide, boric acid, water glass, phosphoric acid, chloride, etc., organic phosphates, bromine compounds, guanidines, etc. occupy the majority, and oil-based flame retardants derived from plants Currently, there is no such knowledge, and plant materials are degraded by microorganisms.

発明が解決しようとする課題Problems to be solved by the invention

環境にとって好ましい植物系難燃化化合物を選定する。選定された植物系の化合物と共にネットワークする環境に負荷をかけない無機化合物の選定によって分子量が向上する組成配合比を構成する。その何れも高価であってはならず、リサイクル性も考慮した研究に着手。
また、耐水性も求められる場合は環境を鑑みエマルジョン系ポリマーを主に選定し、環境に優しい素材の組み合わせに配慮する。この操作によって相溶性が優れる塗膜や接着剤が得られ耐熱性、難燃性、不燃性レベルの高い素材を得ることを課題とする。
Select plant-based flame retardant compounds that are favorable to the environment. A composition blending ratio that increases the molecular weight is selected by selecting an inorganic compound that does not place a burden on the network environment with the selected plant compound. Neither of them should be expensive, and research into consideration of recyclability has begun.
In addition, when water resistance is also required, an emulsion polymer is mainly selected in consideration of the environment, and consideration is given to a combination of environmentally friendly materials. By this operation, a coating film or an adhesive having excellent compatibility is obtained, and an object is to obtain a material having a high level of heat resistance, flame retardancy, and incombustibility.

課題を解決する為の手段Means to solve the problem

本発明の植物油脂系難燃剤の構成において有効な素材として、ラウリン酸含有量が勝る椰子油、パーム核油系洗濯石鹸粉末、薬用石鹸粉砕粉末、水酸化アルミニュウム、酸化マグネシュム、ポリ塩化アルミニュウム、アルミナなど有効、経済的な組み合わせが見出された。
以上、前記記載の植物油脂系難燃剤を構成する主要原料である。
(A)難燃剤SAの重量比組成(代表例)と配合手順を以下に示す。
ラウリン酸含有洗濯粉石鹸(以下Sと略称)40部:水24部:水酸化アルミニュウム30部:酸化マグネシュウム6部(重量部)
A−1、前記粉石鹸S40部に水40部を加え水酸化アルミニュウム30部を加え良く攪拌する。水酸化アルミニュウムを加えると反応熱(約26〜30℃±)が生じる。
A−2、前記の反応熱が継続している時点で酸化マグネシュウム6部を加え安定させる。
この難燃性組成物(以下SAと略称)を塗膜として金属、非極性樹脂以外の被着体に塗布した場合、被着体に接着し塗膜は相互結合し安定する。
この難燃性塗膜に1,400℃バーナを5分間照射しても燃えず溶融せず無煙性である。
As an effective material in the composition of the vegetable oil-based flame retardant of the present invention, coconut oil, palm kernel oil-based laundry soap powder, medicinal soap pulverized powder, aluminum hydroxide, magnesium oxide, polyaluminum chloride, alumina having a higher lauric acid content An effective and economical combination was found.
As mentioned above, it is a main raw material which comprises the said vegetable oil-based flame retardant.
(A) The weight ratio composition (representative example) and the blending procedure of the flame retardant SA are shown below.
Lauric acid-containing laundry powder soap (hereinafter abbreviated as S) 40 parts: Water 24 parts: Aluminum hydroxide 30 parts: Magnesium oxide 6 parts (parts by weight)
A-1, 40 parts of water is added to 40 parts of the soap bar, 30 parts of aluminum hydroxide is added and stirred well. When aluminum hydroxide is added, reaction heat (about 26-30 ° C. ±) is generated.
A-2, 6 parts of magnesium oxide is added and stabilized when the heat of reaction continues.
When this flame retardant composition (hereinafter abbreviated as SA) is applied as a coating to an adherend other than a metal or non-polar resin, it adheres to the adherend and the coating is interconnected and stabilized.
Even if this flame retardant coating film is irradiated with a 1,400 ° C. burner for 5 minutes, it does not burn and does not melt.

前記の配合比に限らずS35〜55部:水20〜30部:水酸化アルミニュム20〜35部:酸化マグネシュム2〜8部近似の重量比でも良いが限定されるものではない。(請求項1)The weight ratio is not limited to S35 to 55 parts: water 20 to 30 parts: aluminum hydroxide 20 to 35 parts: magnesium oxide 2 to 8 parts. (Claim 1)

前記組成物SA20〜25部:エマルジョン系ポリマー75〜80部を均一混合する。
飽和脂肪酸のもつ界面活性効果で相溶性が良く均一に相溶する。
前記乾燥した塗膜1400℃バーナー面照射30秒間不燃無煙性で炭化する。
試験体エマルジョンポリマーは、アクリル系、ウレタン系、EVA系など。
20 to 25 parts of the composition SA: 75 to 80 parts of an emulsion polymer are uniformly mixed.
Good compatibility and uniform compatibility due to the surface active effect of saturated fatty acids.
The dried coating is carbonized with 1400 ° C. burner surface irradiation for 30 seconds incombustible and smokeless.
Specimen emulsion polymer is acrylic, urethane, EVA, etc.

(B)難燃剤のSP重量組成比(代表例)を以下に示す。
B−1、粉石鹸S15〜20部:PAC30〜40部:水酸化アルミニュウム20〜45部
B−2、SにPACを添加すると一時的に膨潤反応する。反応時に水酸化アルミニュウムを添加攪拌する操作で膨潤反応が終息する。この組成物を以下、SPと略称する。(請求項2)
(B) SP weight composition ratio (representative example) of the flame retardant is shown below.
B-1, Powdered soap S15-20 parts: PAC 30-40 parts: Aluminum hydroxide 20-45 parts B-2, When PAC is added to S, a swelling reaction occurs temporarily. The swelling reaction is terminated by adding and stirring aluminum hydroxide during the reaction. Hereinafter, this composition is abbreviated as SP. (Claim 2)

前記、SP18〜25部:エマルジョン系ポリマー75〜82部均一にブレンドする。
SP添加量が22部以上であれば1,400℃接炎30秒間不燃、無溶融、無煙性でエマルジョン系ポリマーは超難燃化する。(燃焼認定垂直試験UL94 V−0)
試験体エマルジョンポリマーは、アクリル系、ウレタン系、EVA系など全て超難燃化有効。
SP18-25 parts: Emulsion polymer 75-82 parts uniformly blended.
If the amount of SP added is 22 parts or more, the emulsion polymer is non-flammable, non-melting, and smoke-free at 1,400 ° C. for 30 seconds, making it extremely flame-retardant. (Combustion certified vertical test UL94 V-0)
Specimen emulsion polymer is super flame retardant effective for acrylic, urethane, EVA, etc.

B−3、粉石鹸S30部:PAC50部:エマルジョンポリマー20部を均一に攪拌する。
前記組成物をウレタンフォーム材(独立気泡体)の表面層に塗布した。塗膜乾燥後、20秒間接炎しても可燃性のフォーム材にも着火せず熱溶融せず無煙であり熱分解ガスの発生がない状況である。(ブレンド使用材料:アクリルエマルジョン系耐熱100℃クラス)
B-3, powdered soap S30 parts: PAC 50 parts: Emulsion polymer 20 parts are stirred uniformly.
The said composition was apply | coated to the surface layer of urethane foam material (closed cell body). Even after 20 seconds of indirect flame after drying the coating, the flammable foam material does not ignite, does not melt, is smokeless, and does not generate pyrolysis gas. (Blend material: acrylic emulsion heat-resistant 100 ° C class)

作用Action

炭素数12のラウリン酸48%±を含有する椰子油、パーム核油、動物油脂系固形石鹸(R−CHCOOM)は水分率も高く接炎しても燃焼しないが水分と共に熱溶融流動する又連続接炎で含有水分が完全に気化すると接炎によって炭化する。
一方ラウリン酸含有量が少ない合成洗濯粉石鹸は僅か2秒の接炎によって燃焼するが激しく燃え上がる現象はない。この現象はニートソープから成る石鹸成分中ラウリン酸(酢酸メチル基)の可燃性分解ガス発生量が極めて少ないことを意味する。したがってラウリン酸含有量によって可燃性、難燃性能が左右されることが判断可能。しかし液状洗濯洗浄剤は結晶化阻害剤としてグリセリンやアルコールなどが含まれている為、激しく燃焼する。
Coconut oil, palm kernel oil, and animal fat-based solid soap (R-CH 2 COOM) containing lauric acid 48% ± with 12 carbon atoms have a high moisture content and do not burn even when in contact with flames, but heat melt and flow with moisture In addition, when the moisture content is completely vaporized by continuous flame contact, it carbonizes due to flame contact.
On the other hand, synthetic laundry soap with a low lauric acid content burns by flame contact for only 2 seconds, but there is no flaming phenomenon. This phenomenon means that the amount of flammable decomposition gas generated from lauric acid (methyl acetate group) in soap components composed of neat soap is extremely small. Therefore, it can be judged that flammability and flame retardancy are affected by the content of lauric acid. However, liquid laundry detergents burn violently because they contain glycerin and alcohol as crystallization inhibitors.

前記の様な反応から推察してもラウリン酸を50%±含有する(カルボン酸のナトリュムやカリウムの塩)結晶化ニートソープから成る石鹸粉末(結晶)に対し水溶性無機高分子、或いは金属酸化物系無機フィラーを混合相溶する操作で超難燃性或いは不燃性組成物が得られる。Inferred from the reaction as described above, water-soluble inorganic polymer or metal oxide is contained in soap powder (crystal) made of crystallized neat soap containing 50% ± lauric acid (sodium carboxylic acid or potassium salt). A super-flame retardant or non-flammable composition can be obtained by mixing and mixing physical inorganic fillers.

熱分解ガス量の少ないラウリン酸と不燃性無機高分子或いは金属酸化物系無機フィラーなどを混合相溶させた化合物をエマルジョン系ポリマーに対し重量比22%以上添加する操作でポリマー成分中に脂肪酸の界面活性効果相溶化でラウリン酸と無機高分子と有機高分子が結合する。この高分子量化した耐熱向上効果と可燃性ポリマー成分の全体比の低減及び金属酸化物無機フィラー分布範囲占有量とのプラス相乗効果と推察される。
接炎時の状況においての難燃メカニズムは脱水吸熱反応による酸化反応場ポリマー成分中の分解ガスの発生を抑制し火炎による熱伝播を遮断するものと考えられる。
By adding a compound in which lauric acid with a small amount of pyrolysis gas and a non-combustible inorganic polymer or metal oxide inorganic filler is mixed and mixed with the emulsion polymer in a weight ratio of 22% or more, the fatty acid in the polymer component is added. Surface active effect compatibilization combines lauric acid, inorganic polymer and organic polymer. This is presumed to be a positive synergistic effect between the high-molecular-weight heat-resistance improving effect, the reduction in the overall ratio of combustible polymer components, and the metal oxide inorganic filler distribution range occupancy.
It is considered that the flame retardant mechanism in the state of contact with flame suppresses the generation of decomposition gas in the oxidation reaction field polymer component due to dehydration endothermic reaction and blocks the heat propagation by the flame.

(第1実施例)
以下、本発明の第1実施例植物油脂系難燃組成物SAの場合を以下に説明する。
1−1 配合比S35部:水30部:水酸化アルミニュム28部:Mgo7部(重量部)
1−2、S35部に水30部を加え攪拌更に水酸化マグネシュウム28部添加攪拌するこの時点で反応熱が発生する更にMgo7部を添加し均一攪拌する。
1−3、この組成物SAをその状態で不燃化した木材片に金属ヘラ冶具にて塗布した。
自然乾燥時間(気温26℃湿度72%±)4時間。木材被着体に良く接着しSA粒P相互も結合し石鹸含有中の香料の香りも保持している。燃焼試験(1400℃バーナー照射接炎2分間)は8時間経過後に実施。SA塗布膜(厚さ2mm±)接炎2分間の結果。
燃焼せず、炭化深さ1mm未満、無溶融、無煙性。被着体木材燃焼せず損傷なし。
(First embodiment)
Hereinafter, the case of 1st Example vegetable oil-based flame retardant composition SA of this invention is demonstrated.
1-1 Mixing ratio S35 parts: water 30 parts: aluminum hydroxide 28 parts: Mgo 7 parts (parts by weight)
1-2, add 30 parts of water to 35 parts of S, stir, and then add 28 parts of magnesium hydroxide and stir. At this point, add 7 parts of Mgo which generates reaction heat and stir uniformly.
1-3, This composition SA was applied to a piece of wood incombustible in that state with a metal spatula jig.
Natural drying time (temperature 26 ° C, humidity 72% ±) 4 hours. It adheres well to the adherend of wood and binds SA grains P to each other and retains the fragrance of the fragrance contained in the soap. The combustion test (1400 ° C burner irradiation flame contact for 2 minutes) was conducted after 8 hours. Results of SA coating film (thickness 2 mm ±) flame contact for 2 minutes.
Does not burn, carbonization depth is less than 1mm, no melting, no smoke. The adherend wood does not burn and is not damaged.

1−4 配合比S30部:水28部:水酸化アルミニュウム37部:Mgo5部
1−5、S30部に水28部を加え攪拌更に水酸化アルミニュウム37部添加攪拌するこの時点で反応熱が発生する更にMgo5部を添加し均一攪拌する。
1−6、この組成物SAを前記同様の不燃化処理木粒子成形体に金ヘラ冶具にて塗布する。
塗膜乾燥、燃焼試験は前記に近似の条件とした。接炎180秒間燃焼せず炭化深さ1mm、無溶融、無煙性。被着体木粒子成形体燃焼せず損傷なし。
1-4 Mixing ratio S30 parts: water 28 parts: aluminum hydroxide 37 parts: Mgo 5 parts 1-5, 28 parts of water is added to S30 part and stirred, and then further 37 parts of aluminum hydroxide is added and stirred. At this point, heat of reaction is generated. Further, 5 parts of Mgo is added and stirred uniformly.
1-6, This composition SA is applied to the incombustible treated wood particle compact as described above with a gold spatula jig.
The coating film drying and combustion test were performed under conditions similar to those described above. It does not burn for 180 seconds, and has a carbonization depth of 1 mm, no melting and no smoke. The adherend wood particle compact does not burn and is not damaged.

1−6、前記配合(1−4)SA25部:ウレタンエマルジョン75部を均一攪拌する。
1−7、試験塗布被着体ジュラルミンに刷毛塗り片面1回塗布。接炎20秒間着火せず、炭化、無溶融、無煙。接炎終了後、1分後ジュラルミン無処理裏面表面温度測定値630℃±。
熱伝導に優れたジュラルミンの上昇温度測定値630℃の半数すなわち300℃以上短時間に耐えるウレタン塗膜が形成されたことが判断可能。従来のリン酸エステルなどの難燃剤は難燃性に寄与するが総じて耐熱性能が劣る様になるが、本発明の植物油脂系難燃剤は確実に耐熱性能も格段に向上することが電気炉による連続耐熱試験によっても証明される。
1-6, blending (1-4) 25 parts of SA: 75 parts of urethane emulsion is stirred uniformly.
1-7, Test coating Apply once to brush adherence duralumin. No contact with flame for 20 seconds, carbonization, no melting, no smoke. 1 minute after completion of flame contact, measured duralumin untreated back surface temperature 630 ° C. ±.
It can be judged that a urethane coating film that can withstand a short time of over 630 ° C, that is, 300 ° C or higher, has been formed. Although conventional flame retardants such as phosphate esters contribute to flame retardancy, the heat resistance performance is generally inferior. However, the vegetable oil-based flame retardant of the present invention reliably improves the heat resistance performance according to the electric furnace. It is also proved by continuous heat test.

(第2実施例)
以下、本発明植物油脂系難燃組成物SPの場合を以下に説明する。
2−1 配合比 粉石鹸S22部:PAC40部:水酸化アルミニュウム38部(重量比)
2−2 粉石鹸S22部に対しPAC40部を均一攪拌すると膨潤するが水酸化アルミニュウム38部を加え均一攪拌して安定させる。
(Second embodiment)
Hereinafter, the case of this invention vegetable oil-based flame retardant composition SP is demonstrated.
2-1 Mixing ratio Powdered soap S22 parts: PAC 40 parts: Aluminum hydroxide 38 parts (weight ratio)
2-2 When PAC 40 parts are uniformly stirred with respect to S22 parts of powdered soap, it swells, but 38 parts of aluminum hydroxide is added and stirred uniformly to stabilize.

2−3 前記配合のSP20部:アクリルエマルジョン80部を均一攪拌する。
燃焼試験体アルミ箔積層PET不織布の両面に前記組成物を2回追いかけ塗り塗布する。
15時間自然乾燥後、燃焼試験実施。(燃焼テストは照射接炎1分間1,400℃バーナー使用)
試験体PET不織布部分燃焼せず炭化する。アルミ箔燃焼せず炭化する。
2-3 SP 20 parts of the above formulation: 80 parts of the acrylic emulsion is stirred uniformly.
The composition is chased and applied twice on both sides of the flame test specimen aluminum foil laminated PET nonwoven fabric.
After 15 hours of natural drying, a combustion test was conducted. (The combustion test uses a 1,400 ° C burner for 1 minute of irradiation contact)
Specimen PET nonwoven fabric carbonizes without burning. Carbonizes without burning aluminum foil.

2−4 前記配合のSP25部:EVAエマルジョン75部を均一攪拌する。
2−5 燃焼試験体綿生地に片面1回塗布する操作で生地に浸透する。
20時間自然乾燥後、前記同様条件で燃焼試験実施。綿生地は燃焼せず炭化する。
2-4 SP25 part of the above formulation: 75 parts of EVA emulsion is uniformly stirred.
2-5 Combustion test It penetrates into the fabric by the operation of applying one side to the cotton fabric once.
After natural drying for 20 hours, a combustion test was conducted under the same conditions as described above. Cotton fabric does not burn and carbonizes.

2−6、粉石鹸S25部:PAC60部:ウレタンエマルジョン15部を均一攪拌する。
2−7、燃焼試験体PE独立気泡フォーム材を前記組成物中に浸し軽く絞り乾燥させる。
前記同様条件で燃焼試験実施。熱に弱いPEフォーム材燃焼せず無煙炭化する。
2-6, powdered soap S25 parts: PAC 60 parts: Urethane emulsion 15 parts are stirred uniformly.
2-7, The combustion test body PE closed cell foam material is dipped in the composition and lightly squeezed to dry.
A combustion test was conducted under the same conditions as above. PE foam material that is weak to heat does not burn and smokeless carbonizes.

2−8、粉石鹸S30部:PAC55部:EVAエマルジョン15部を均一攪拌する。
2−9、燃焼試験体PS発泡体の表面層に(塗膜厚さ0,4mm±)2層膜を形成する。
前記同様条件で燃焼試験実施。通常簡単に黒煙を上げ延焼熱溶融するPS発泡体が黒煙を上げず燃焼しないが約3秒を経過する時点から熱収縮する。この結果からも超難燃耐熱シールド層がポリマー相溶前記ブレンド組成物によって形成されたことが判断可能。
2-8, powdered soap S30 parts: PAC 55 parts: EVA emulsion 15 parts are uniformly stirred.
2-9, a two-layer film (coating thickness 0,4 mm ±) is formed on the surface layer of the combustion test specimen PS foam.
A combustion test was conducted under the same conditions as above. Normally, PS foam which simply raises black smoke and spreads and heat melts does not raise black smoke and does not burn, but heat shrinks after about 3 seconds. From this result, it can be judged that the super-flame retardant heat-resistant shield layer was formed from the polymer-compatible blend composition.

本発明の応用として可燃性或いは熱溶融する素材に含浸或いは粗粉砕した可燃素材に被膜を形成させる方法で熱分解させると炭素化して黒く手に付着しない各素材に応じた特性や個性のある新たな素材として各種高温耐酸化性耐熱カーボン素材が生まれる。
また、焼成カーボン化する炉内は素材が熱溶融しない為、炉内が損傷しない。
As an application of the present invention, a new material having characteristics and individuality according to each material that is carbonized and does not adhere to the hand when it is pyrolyzed by a method of forming a film on a combustible material that has been impregnated or coarsely pulverized into a combustible or heat-melting material. Various high-temperature oxidation-resistant heat-resistant carbon materials are born as new materials.
Moreover, since the raw material is not melted in the furnace for carbonization, the furnace is not damaged.

PACは、金属酸化物半導体性液体でもありその含有量によってSP含有塗膜或いは接着剤は導電性機能を発揮する。PAC is also a metal oxide semiconducting liquid, and depending on its content, the SP-containing coating film or adhesive exhibits a conductive function.

この技術の応用範囲は広くエマルジョン系ポリマーの超難燃化以外に本発明の植物油脂系難燃剤粒子の吸着水分を飛ばし微粉砕(30μ±)して練り込みする工業的操作で溶剤系塗装材料、熱硬化性レジン、熱可塑性ポリマー系にも有効である。その理由は、油脂系固有の界面活性効果によるポリマーとの相溶化が容易であるからである。
以上、本発明の実施例を説明してきたが、具体的な構成は、本発明の実施例に限らず、要旨を逸脱しない範囲における追加、変更があっても本発明に含まれる。
The application range of this technology is wide. Besides the super-flame retardant of emulsion polymer, solvent-based coating material is applied by industrial operation to remove the adsorbed moisture of the vegetable oil-based flame retardant particles of the present invention and finely pulverize (30μ ±). It is also effective for thermosetting resins and thermoplastic polymer systems. The reason is that compatibilization with the polymer is easy due to the surface active effect inherent in the oil and fat system.
Although the embodiments of the present invention have been described above, specific configurations are not limited to the embodiments of the present invention, and additions and changes within the scope of the present invention are included in the present invention.

発明の効果The invention's effect

本発明の植物油脂系難燃剤の組成割合においてラウリン酸含有石鹸質素材と金属酸化物系無機高分子や金属酸化物系無機フィラーとの間に技術的に絶妙な組み合わせが有り、この極めて地味な創造と実験の積み重ねが超耐熱難燃性素材を創作させたものである。In the composition ratio of the vegetable oil-based flame retardant of the present invention, there is a technically exquisite combination between the lauric acid-containing soapy material and the metal oxide inorganic polymer or metal oxide inorganic filler. Creation of super heat-resistant flame retardant material is the result of repeated creation and experimentation.

可燃性が懸念される各種素材に対し耐熱、難燃性シールド層が簡易塗装で形成可能。火災発生時、耐炎無煙性の防火塗料として延焼防止効果が期待できる。A heat-resistant and flame-retardant shield layer can be formed by simple coating for various materials that may be flammable. In the event of a fire, a fire spread prevention effect can be expected as a flameproof and smokeless fireproof paint.

耐炎シールド塗料の他、汎用レベルの各種ポリマーや熱硬化性レジンが本発明SP素材とある種の無機フィラーを追加配合する操作によって硬質化させた素材は熱無溶融、不燃性、超耐熱素材(例:アクリル樹脂、電気炉連続24時間耐熱試験400℃キープする)となる。In addition to flame-resistant shield paints, materials made by adding various kinds of polymers and thermosetting resins to the SP material of the present invention and certain inorganic fillers are hardened by heat non-melting, non-flammable, super heat-resistant materials ( Example: Acrylic resin, electric furnace continuous 24 hours heat test 400 ° C keep).

本発明難燃剤に微生物に対して殺菌作用を持つ殺菌剤として塩化ベンザルコニウム、アルキルリン酸化ベンザルコニウム等を複合する操作で除菌効果に優れた薬用不燃塗膜の形成や除菌機能に優れた超難燃性ポリマーが創作できる。高齢者医療施設などの医療機関の天井や内壁素材として有効。For the formation and sterilization function of medicinal incombustible coatings with excellent sterilization effect by combining benzalkonium chloride, alkylphosphorylated benzalkonium etc. Excellent super flame retardant polymer can be created. Effective as a ceiling or inner wall material for medical institutions such as medical facilities for the elderly.

本発明難燃剤を定着した条件下で高温酸化性雰囲気で熱分解カーボン化する技術効果は優れた高温耐酸化性超耐熱素材を生む。
また、使用の限界を超えたこれら素材の粉砕細粒物は炭素化温度領域を1000℃クラスでカーボン化処理する操作で不燃性活性炭、不燃性耐熱フィラー、不燃性導電性カーボン素材としても多彩な再利用が可能である。(マテリアルリサイクル性)
完全に熱分解を伴って焼成されたカーボン素材は、生体不活性であり、医療用途等にも応用可能な製品となる可能性を持っている。
The technical effect of pyrolytic carbonization in a high temperature oxidizing atmosphere under the conditions where the flame retardant of the present invention is fixed produces an excellent high temperature oxidation resistant super heat resistant material.
In addition, the finely pulverized fine particles of these materials exceeding the limits of use are various as non-combustible activated carbon, non-combustible heat-resistant filler, non-combustible conductive carbon material by the operation of carbonizing in the carbonization temperature range at 1000 ° C class. Can be reused. (Material recyclability)
Carbon materials that have been completely fired with pyrolysis are inactive and have the potential to become products that can be used for medical purposes.

Claims (2)

ラウリン酸含有植物油脂系石鹸質素材と水、金属酸化物系フイラーを複合化することを特徴とする難燃性組成物。  A flame-retardant composition comprising a composite of a lauric acid-containing vegetable oil-based soapy material, water, and a metal oxide filler. ラウリン酸含有植物油脂系石鹸質素材とPAC,金属酸化物系無機フィラーを複合することを特徴とする難燃剤。  A flame retardant comprising a composite of a lauric acid-containing vegetable oil-based soapy material, PAC, and a metal oxide-based inorganic filler.
JP2006312211A 2006-10-22 2006-10-22 Flame retardant based on vegetable oil and fat Pending JP2008101179A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009128306A1 (en) * 2008-04-16 2009-10-22 株式会社Hi-Van Composite material for imparting flame retardancy
CN103436270A (en) * 2013-08-19 2013-12-11 太原理工大学 Method for preparing core-shell type flame retardant

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6346291A (en) * 1986-08-12 1988-02-27 ラリ−・ジ−・エスカインド Fire retardant composition and its use
JP2003226877A (en) * 2002-02-05 2003-08-15 Yamamoto Kagu Seisakusho:Kk Aqueous flame proof/flame retardant agent
JP2004099703A (en) * 2002-09-06 2004-04-02 Mitsubishi Plastics Ind Ltd Flame-retardant resin composition and flame-retardant molded article
JP2005179597A (en) * 2003-12-22 2005-07-07 Sekisui Chem Co Ltd Noncombustible sheet material
WO2006073203A1 (en) * 2005-01-05 2006-07-13 Fukuoka Prefectural Government Liquid composition for water-repellent treatment of wood and method for water-repellent treatment of wood, and water-repellent treated wood and product using water-repellent treated wood

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6346291A (en) * 1986-08-12 1988-02-27 ラリ−・ジ−・エスカインド Fire retardant composition and its use
JP2003226877A (en) * 2002-02-05 2003-08-15 Yamamoto Kagu Seisakusho:Kk Aqueous flame proof/flame retardant agent
JP2004099703A (en) * 2002-09-06 2004-04-02 Mitsubishi Plastics Ind Ltd Flame-retardant resin composition and flame-retardant molded article
JP2005179597A (en) * 2003-12-22 2005-07-07 Sekisui Chem Co Ltd Noncombustible sheet material
WO2006073203A1 (en) * 2005-01-05 2006-07-13 Fukuoka Prefectural Government Liquid composition for water-repellent treatment of wood and method for water-repellent treatment of wood, and water-repellent treated wood and product using water-repellent treated wood

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009128306A1 (en) * 2008-04-16 2009-10-22 株式会社Hi-Van Composite material for imparting flame retardancy
CN103436270A (en) * 2013-08-19 2013-12-11 太原理工大学 Method for preparing core-shell type flame retardant
CN103436270B (en) * 2013-08-19 2015-06-10 太原理工大学 Method for preparing core-shell type flame retardant

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