JPH04249550A - Encapsulated flame retardant - Google Patents
Encapsulated flame retardantInfo
- Publication number
- JPH04249550A JPH04249550A JP40943490A JP40943490A JPH04249550A JP H04249550 A JPH04249550 A JP H04249550A JP 40943490 A JP40943490 A JP 40943490A JP 40943490 A JP40943490 A JP 40943490A JP H04249550 A JPH04249550 A JP H04249550A
- Authority
- JP
- Japan
- Prior art keywords
- flame retardant
- inorganic
- flame retardants
- building materials
- blended
- 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
Links
- 239000003063 flame retardant Substances 0.000 title claims abstract description 61
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 239000002245 particle Substances 0.000 claims abstract description 26
- 239000012796 inorganic flame retardant Substances 0.000 claims abstract description 19
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims abstract description 9
- 239000004033 plastic Substances 0.000 claims abstract description 8
- 229920003023 plastic Polymers 0.000 claims abstract description 8
- 239000000835 fiber Substances 0.000 claims abstract description 6
- 239000000123 paper Substances 0.000 claims abstract description 6
- 239000005060 rubber Substances 0.000 claims abstract description 6
- 239000002023 wood Substances 0.000 claims abstract description 6
- 239000003094 microcapsule Substances 0.000 claims abstract description 5
- 239000004566 building material Substances 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 abstract description 8
- 238000000576 coating method Methods 0.000 abstract description 8
- 239000004035 construction material Substances 0.000 abstract 2
- 229920003002 synthetic resin Polymers 0.000 description 11
- 239000000057 synthetic resin Substances 0.000 description 11
- 229910052736 halogen Inorganic materials 0.000 description 9
- 150000002367 halogens Chemical class 0.000 description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 8
- 230000000704 physical effect Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 239000011574 phosphorus Substances 0.000 description 6
- 229910052698 phosphorus Inorganic materials 0.000 description 6
- 239000000779 smoke Substances 0.000 description 6
- 239000002341 toxic gas Substances 0.000 description 5
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 4
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 4
- 238000002845 discoloration Methods 0.000 description 4
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 4
- -1 For safety reasons Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- IVORCBKUUYGUOL-UHFFFAOYSA-N 1-ethynyl-2,4-dimethoxybenzene Chemical compound COC1=CC=C(C#C)C(OC)=C1 IVORCBKUUYGUOL-UHFFFAOYSA-N 0.000 description 2
- LIAWCKFOFPPVGF-UHFFFAOYSA-N 2-ethyladamantane Chemical compound C1C(C2)CC3CC1C(CC)C2C3 LIAWCKFOFPPVGF-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QBLDFAIABQKINO-UHFFFAOYSA-N barium borate Chemical compound [Ba+2].[O-]B=O.[O-]B=O QBLDFAIABQKINO-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- HQUQLFOMPYWACS-UHFFFAOYSA-N tris(2-chloroethyl) phosphate Chemical compound ClCCOP(=O)(OCCCl)OCCCl HQUQLFOMPYWACS-UHFFFAOYSA-N 0.000 description 2
- NZUPFZNVGSWLQC-UHFFFAOYSA-N 1,3,5-tris(2,3-dibromopropyl)-1,3,5-triazinane-2,4,6-trione Chemical compound BrCC(Br)CN1C(=O)N(CC(Br)CBr)C(=O)N(CC(Br)CBr)C1=O NZUPFZNVGSWLQC-UHFFFAOYSA-N 0.000 description 1
- RVHUMFJSCJBNGS-UHFFFAOYSA-N 2-[2,6-dibromo-4-[2-[3,5-dibromo-4-(2-hydroxyethoxy)phenyl]propan-2-yl]phenoxy]ethanol Chemical compound C=1C(Br)=C(OCCO)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(OCCO)C(Br)=C1 RVHUMFJSCJBNGS-UHFFFAOYSA-N 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明はプラスチック、ゴム、繊
維、紙、木材等の建材等に配合してこれらを難燃化する
難燃剤に係り、特に、無機系難燃剤の母粒子をポリマ系
難燃剤の子粒子で被覆したカプセル型難燃剤に関する。[Industrial Application Field] The present invention relates to flame retardants that are blended into building materials such as plastics, rubber, fibers, paper, and wood to make them flame retardant. This invention relates to a capsule-type flame retardant coated with flame retardant child particles.
【0002】0002
【従来の技術】一般にプラスチック、ゴム、繊維、紙、
木材等の建材等には安全性の見地から難燃剤を混合して
難燃化されている。[Prior art] Plastics, rubber, fibers, paper,
For safety reasons, building materials such as wood are mixed with flame retardants to make them flame retardant.
【0003】この難燃剤はその使用方法により添加法と
反応法に分けられる。添加法は難燃剤をポリマに添加し
て使用するものであり、添加量によってはプラスチック
の物性を変化させる可能性があるが、ハンドリングが容
易であるといったメリットがある。一方、反応法はプラ
スチックの製造時に反応させるものであり、添加法の如
くプラスチックの物性を変化させる虞はないが官能基を
有する化合物であるため、製造が難しく値段も高くなる
傾向がある。[0003] This flame retardant can be classified into an additive method and a reaction method depending on its method of use. The addition method involves adding a flame retardant to the polymer, which may change the physical properties of the plastic depending on the amount added, but has the advantage of being easy to handle. On the other hand, the reaction method involves reacting during the production of plastics, and unlike the addition method, there is no risk of changing the physical properties of the plastic, but since it involves a compound with a functional group, it tends to be difficult to produce and expensive.
【0004】また、この難燃剤を成分上から大きく分類
すると、ハロゲン系難燃剤、リン系難燃剤のポリマ系難
燃剤と、無機系難燃剤の2つに分けられる。[0004]Furthermore, flame retardants can be broadly classified into two types: halogen-based flame retardants, phosphorus-based flame retardants, or polymer-based flame retardants, and inorganic flame retardants.
【0005】ポリマ系難燃剤の代表的なものとして、テ
トラブロモビスフェノールA(TBA)、ヘキサブロモ
ベンゼン(HBB)、トリクレジルホスフェート(TC
P)、トリエチルホスフェート(TEP)などのポリマ
ータイプが挙げられる。また、無機系難燃剤の代表的な
ものとして水酸化アルミニウム、水酸化ジルコニウム、
水酸化マグネシウム、赤リン、酸化スズ、三酸化アンモ
ン、メタホウ酸バリウム等が挙げられる。Typical polymeric flame retardants include tetrabromobisphenol A (TBA), hexabromobenzene (HBB), and tricresyl phosphate (TC).
P), triethyl phosphate (TEP), and other polymer types. In addition, typical inorganic flame retardants include aluminum hydroxide, zirconium hydroxide,
Examples include magnesium hydroxide, red phosphorus, tin oxide, ammonium trioxide, barium metaborate, and the like.
【0006】ところで、これら難燃剤を建材などに配合
する場合、ハロゲン系難燃剤、リン系難燃剤のポリマ系
難燃剤と、無機系難燃剤は適当に複合されて配合されて
いる。すなわち、建材などに配合する難燃剤を無機系難
燃剤のみを使用した場合、無機系難燃剤は製造プロセス
により、無機粉体表面が化学的に中性でない可能性があ
り、この場合、無機系難燃剤が配合される建材などと化
学反応を起こし、配合される建材などに着色を与えたり
物性を低下させる発生率が多くなる傾向がある。一方、
配合する難燃剤をポリマータイプであるハロゲン系難燃
剤、リン系難燃剤のみを使用した場合、発火時に発煙及
び有毒ガスの発生率が多くなってしまう虞がある。また
、このハロゲン系難燃剤、リン系難燃剤は紫外線に晒さ
れた場合、配合される建材などを変色させ、またその物
性も低下させるといった欠点を有している。しかも粉体
特性としての流動性がハンドリング上問題となる。By the way, when these flame retardants are blended into building materials, polymer flame retardants such as halogen flame retardants and phosphorus flame retardants, and inorganic flame retardants are appropriately combined and blended. In other words, if only inorganic flame retardants are used as flame retardants in building materials, the surface of the inorganic powder may not be chemically neutral due to the manufacturing process; There is a tendency for flame retardants to cause chemical reactions with the building materials to which they are blended, resulting in coloring and deterioration of physical properties of the building materials to which they are blended. on the other hand,
If only polymer-type halogen-based flame retardants or phosphorus-based flame retardants are used as flame retardants, there is a risk that the rate of smoke and toxic gas generation will increase upon ignition. Furthermore, these halogen-based flame retardants and phosphorus-based flame retardants have the disadvantage that, when exposed to ultraviolet rays, they discolor building materials, etc. in which they are blended, and also deteriorate their physical properties. Moreover, fluidity as a powder characteristic poses a handling problem.
【0007】このため、特開昭61−115942では
図2に示すように、ハロゲン系難燃剤粉末aを合成樹脂
bで被膜しマイクロカプセルすると共に、この合成樹脂
被膜bに微粒子状の水酸化アルミニウム等の無機系難燃
剤cを合成樹脂bに対して5〜100wt%を含有させ
ることによってハロゲン系難燃剤粉末aの耐光性及び流
動特性を向上させたカプセル型難燃剤が提案されている
。For this reason, in JP-A-61-115942, as shown in FIG. 2, a halogen flame retardant powder a is coated with a synthetic resin b to form microcapsules, and fine particles of aluminum hydroxide are added to the synthetic resin coat b. A capsule-type flame retardant has been proposed in which the light resistance and flow characteristics of the halogen-based flame retardant powder a are improved by containing an inorganic flame retardant c such as 5 to 100 wt % based on the synthetic resin b.
【0008】[0008]
【発明が解決しようとする課題】ところで、特開昭61
−115942にあっては、ポリマーの使用量が多くな
ってしまい、発火時に煙りや有毒ガスの発生量が多くな
ってしまう欠点があった。また、合成樹脂b被膜に含有
させる水酸化アルミニウム等の無機系難燃剤cは粒径が
サブミクロン〜数μといった極めて小さい粒径ものが必
要であり、製造が困難であるため、非常に高価なもので
あった。さらに、この水酸化アルミニウム等の金属酸化
物、水酸化物等の微粒子fが上記合成樹脂b被膜の表面
にもかなり存在する可能性があり、水酸化物等の微粒子
表面のpH経時変化が進み、合成樹脂b被膜の表面が変
色する可能性があった。[Problem to be solved by the invention] By the way, JP-A-61
-115942 had the disadvantage that a large amount of polymer was used, resulting in a large amount of smoke and toxic gas being generated when ignited. In addition, the inorganic flame retardant (c) such as aluminum hydroxide contained in the synthetic resin (b) coating must have an extremely small particle size of submicrons to several microns, which is difficult to manufacture and therefore extremely expensive. It was something. Furthermore, there is a possibility that a considerable amount of fine particles f of metal oxides and hydroxides such as aluminum hydroxide exist on the surface of the synthetic resin b coating, and the pH of the surface of fine particles such as hydroxides changes over time. There was a possibility that the surface of the synthetic resin b coating would change color.
【0009】そこで、本発明は上述した問題点を有効に
解決するために案出されたものであり、その目的は合成
樹脂等のポリマーの使用量を少なくして発煙や有害ガス
の発生量を低減すると共に、配合する建材などに変色や
物性の低下等の不都合を及ぼさないカプセル型難燃剤を
提供することにある。Therefore, the present invention was devised to effectively solve the above-mentioned problems, and its purpose is to reduce the amount of smoke and harmful gases generated by reducing the amount of polymers such as synthetic resins used. It is an object of the present invention to provide a capsule-type flame retardant that reduces the amount of heat used and does not cause disadvantages such as discoloration or deterioration of physical properties to the building materials in which it is mixed.
【0010】0010
【課題を解決するための手段】上記目的を達成するため
に本発明はプラスチック、ゴム、繊維、紙、木材等の建
材等に配合してこれらを難燃化させる難燃剤において、
水酸化アルミニウム等の無機系難燃剤の母粒子を、ポリ
マ系難燃剤の子粒子で被覆すると共に、マイクロカプセ
ル化したものである。[Means for Solving the Problems] In order to achieve the above object, the present invention provides a flame retardant that is blended into building materials such as plastics, rubber, fibers, paper, and wood to make them flame retardant.
Mother particles of an inorganic flame retardant such as aluminum hydroxide are coated with child particles of a polymer flame retardant and are microencapsulated.
【0011】[0011]
【作用】以上のように本発明では無機系難燃剤の母粒子
をポリマ系難燃剤の子粒子で被覆してマイクロカプセル
化したため、発煙や有毒ガスの発生量を低減させること
ができる。また、ポリマ系難燃剤が無機系難燃剤の酸成
分あるいはアルカリ成分の溶出を防止するため、配合さ
れる建材などを変色や物性の低下等の発生を防止するこ
とができる。さらに、マイクロカプセル化することによ
り、流動特性が向上する。[Function] As described above, in the present invention, the mother particles of an inorganic flame retardant are coated with child particles of a polymer flame retardant to form microcapsules, so that the amount of smoke and toxic gas generated can be reduced. Furthermore, since the polymeric flame retardant prevents the acid component or alkaline component of the inorganic flame retardant from leaching out, it is possible to prevent discoloration and deterioration of physical properties of the building materials to which it is blended. Furthermore, microencapsulation improves flow properties.
【0012】0012
【実施例】以下、本発明の一実施例を添付図面に基づい
て詳述する。DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the present invention will be described below in detail with reference to the accompanying drawings.
【0013】図1に示すように、本発明にかかるカプセ
ル型難燃剤1は水酸化アルミニウム等の無機系難燃剤の
母粒子2を、ハロゲン系難燃剤、リン系難燃剤等のポリ
マ系難燃剤の子粒子3で被覆して、マイクロカプセル化
したものである。As shown in FIG. 1, the capsule-type flame retardant 1 according to the present invention combines base particles 2 of an inorganic flame retardant such as aluminum hydroxide with a polymeric flame retardant such as a halogen flame retardant or a phosphorus flame retardant. It is coated with child particles 3 and microencapsulated.
【0014】この無機系難燃剤は上述したように、水酸
化アルミニウム、水酸化ジルコニウム、水酸化マグネシ
ウム、赤リン、酸化スズ、三酸化アンモン、メタホウ酸
バリウム等であり、その粒径は50〜100μのものが
使用される。As mentioned above, this inorganic flame retardant is aluminum hydroxide, zirconium hydroxide, magnesium hydroxide, red phosphorus, tin oxide, ammonium trioxide, barium metaborate, etc., and its particle size is 50 to 100 μm. are used.
【0015】また、ハロゲン系難燃剤、リン系難燃剤等
のポリマ系難燃剤は上述したテトラブロモビスフェノー
ルA(TBA)、ヘキサブロモベンゼン(HBB)、ト
リクレジルホスフェート(TCP)、トリエチルホスフ
ェート(TEP)の他に2,2−ビス(4−ヒドロキシ
3,5−ジプロフェニル)プロパン、トリス(2,3−
ジブロモプロピル)イソシアヌレート(TAIC−6B
)、2,2ビス(4−ヒドロキシエトキシ−3,5−ジ
ブロモフェニル)プロパン(TBA−EO)、デカブロ
モジフェニルオキサイド(DBDPO)、含ハロゲンポ
リフォスフェート、トリス(β−クロロエチル)ホスフ
ェート(TCEP)、トリスクロロエチルホスフェート
(CLP)、トリスジクロロプロピルホスフェート(C
RP)、クレジルジフェニルホスフェート(CDP)、
キシレニルジフェニルホスフェート(XDP)、酸性リ
ン酸エステル、含窒素リン化合物等があり、粒径が10
μ以下のものが使用される。Polymer flame retardants such as halogen flame retardants and phosphorus flame retardants include the above-mentioned tetrabromobisphenol A (TBA), hexabromobenzene (HBB), tricresyl phosphate (TCP), and triethyl phosphate (TEP). ), 2,2-bis(4-hydroxy3,5-diprophenyl)propane, tris(2,3-
dibromopropyl) isocyanurate (TAIC-6B
), 2,2bis(4-hydroxyethoxy-3,5-dibromophenyl)propane (TBA-EO), decabromodiphenyl oxide (DBDPO), halogen-containing polyphosphate, tris(β-chloroethyl)phosphate (TCEP) , trischloroethylphosphate (CLP), trisdichloropropylphosphate (C
RP), cresyl diphenyl phosphate (CDP),
There are xylenyl diphenyl phosphate (XDP), acidic phosphate esters, nitrogen-containing phosphorus compounds, etc., and the particle size is 10
μ or less is used.
【0016】次に、本実施例の作用を述べる。Next, the operation of this embodiment will be described.
【0017】本発明のカプセル型難燃剤1は先ず、粒径
が50〜100μの無機系難燃剤の母粒子の周囲に、粒
径が10μ以下ポリマ系難燃剤の子粒子を複数、静電気
法、CVD、PVD、スパッタリング法、及び機械的方
法等で付着させることによって被覆すると共に、マイク
ロカプセル化して製造される。そして、このカプセル型
難燃剤を建材などに添加することによって建材などを難
燃化することになる。このように本発明のカプセル型難
燃剤1では、カプセル化するための合成樹脂等のポリマ
の使用量を低減することができ、発火時の発煙および有
毒ガスの発生量を低減することが可能となると共に、無
機系難燃剤の母粒子の酸成分あるいはアルカリ成分が合
成樹脂被膜の表面に溶出し難くなり、配合される建材な
どを変色や物性の変化等から防止することが可能となる
。また、上記特開昭61−115942で合成樹脂に配
合される無機系難燃剤は粒径がサブミクロン〜数μとい
った極めて小さい粒子であるため、1トン当たりの値段
が数百万円であるのに対し、本発明に使用される無機系
難燃剤は粒径が50〜100μといった比較的大きいた
め、その値段も1トン当たり数万円と安価であり、経済
性の点で優れている。また、難燃剤をマイクロカプセル
化することによってその流動特性が向上するため、配合
の均一化が達成できる。The capsule-type flame retardant 1 of the present invention is prepared by first applying a plurality of child particles of a polymeric flame retardant having a particle size of 10 μm or less around a mother particle of an inorganic flame retardant having a particle size of 50 to 100 μm, using an electrostatic method. It is manufactured by coating by deposition using CVD, PVD, sputtering, mechanical methods, etc., and by microencapsulation. By adding this capsule-type flame retardant to building materials, the materials will be made flame retardant. In this way, the capsule-type flame retardant 1 of the present invention can reduce the amount of polymer such as synthetic resin used for encapsulation, and can reduce the amount of smoke and toxic gas generated at the time of ignition. At the same time, the acid component or alkali component of the base particles of the inorganic flame retardant becomes difficult to elute to the surface of the synthetic resin coating, and it becomes possible to prevent discoloration and changes in physical properties of the building materials to which the flame retardant is blended. In addition, the inorganic flame retardant blended into the synthetic resin in the above-mentioned JP-A-61-115942 has extremely small particle sizes ranging from submicrons to several microns, so the price per ton is several million yen. On the other hand, since the inorganic flame retardant used in the present invention has a relatively large particle size of 50 to 100 microns, its price is low at several tens of thousands of yen per ton, making it excellent in terms of economy. Further, by microcapsulating the flame retardant, its flow characteristics are improved, so that a uniform formulation can be achieved.
【0018】尚、図3に示すように、本発明のカプセル
型難燃剤1を紫外線などの光が照射する場所に用いる建
材等に配合する場合は、上記特開昭61−115942
で開示されたようにポリマ系難燃剤の子粒子3の周囲に
微粒子状の無機系難燃剤4を配合した合成樹脂5で被膜
すれば耐光性を向上させることができる。As shown in FIG. 3, when the capsule-type flame retardant 1 of the present invention is blended into building materials used in places exposed to light such as ultraviolet rays, the above-mentioned Japanese Patent Application Laid-Open No. 61-115942 is used.
As disclosed in , light resistance can be improved by coating the child particles 3 of a polymeric flame retardant with a synthetic resin 5 blended with a particulate inorganic flame retardant 4.
【0019】[0019]
【発明の効果】以上、要するに本発明によれば、ポリマ
の使用量が少ないため、発煙や有毒ガスの発生量を低減
することが可能となると共に、配合される建材などを変
色や物性の変化等から防止することができる。また、マ
イクロカプセル化することによりその流動特性が向上し
、品質の均一化が達成される等といった優れた効果を有
している。[Effects of the Invention] In summary, according to the present invention, since the amount of polymer used is small, it is possible to reduce the amount of smoke and toxic gas generated, and the building materials to which it is mixed can undergo discoloration and change in physical properties. etc. can be prevented from occurring. In addition, microcapsules have excellent effects such as improved flow characteristics and uniform quality.
【図1】本発明の一実施例を示す概略図である。FIG. 1 is a schematic diagram showing an embodiment of the present invention.
【図2】従来のカプセル型難燃剤の一例を示す概略図で
ある。FIG. 2 is a schematic diagram showing an example of a conventional capsule-type flame retardant.
【図3】他の変形実施例を示す概略図である。FIG. 3 is a schematic diagram showing another modified embodiment.
1 カプセル型難燃剤 2 母粒子 3 子粒子 1 Capsule type flame retardant 2 Mother particle 3 Child particle
Claims (1)
等の建材等に配合してこれらを難燃化させる難燃剤にお
いて、水酸化アルミニウム等の無機系難燃剤の母粒子を
、ポリマ系難燃剤の子粒子で被覆すると共に、マイクロ
カプセル化したことを特徴とするカプセル型難燃剤。Claim 1: In a flame retardant that is blended into building materials such as plastics, rubber, fibers, paper, and wood to make them flame retardant, base particles of an inorganic flame retardant such as aluminum hydroxide are combined with a polymer flame retardant. A capsule-type flame retardant characterized by being coated with child particles and encapsulated in microcapsules.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP40943490A JPH04249550A (en) | 1990-12-28 | 1990-12-28 | Encapsulated flame retardant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP40943490A JPH04249550A (en) | 1990-12-28 | 1990-12-28 | Encapsulated flame retardant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04249550A true JPH04249550A (en) | 1992-09-04 |
Family
ID=18518772
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP40943490A Pending JPH04249550A (en) | 1990-12-28 | 1990-12-28 | Encapsulated flame retardant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04249550A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11255955A (en) * | 1998-03-10 | 1999-09-21 | Hitachi Ltd | Capsule type flame retardant and resin composition for encapsulating semiconductor containing the same |
| EP0814531A3 (en) * | 1993-03-30 | 2000-02-16 | Canon Kabushiki Kaisha | Secondary battery |
| JP2006328345A (en) * | 2005-04-27 | 2006-12-07 | Hitachi Chem Co Ltd | Flame retardancy-imparting agent and flame-retardant resin composition |
| WO2008062820A1 (en) * | 2006-11-21 | 2008-05-29 | Autonetworks Technologies, Ltd. | Flame retardant, flame retardant composition, insulated wire, wiring harness, and method for producing flame retardant composition |
| US7828995B2 (en) * | 2003-10-02 | 2010-11-09 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Composition for a fire-protection agent for materials and fire-protection method |
| JP2012036398A (en) * | 2005-04-27 | 2012-02-23 | Hitachi Chem Co Ltd | Flame retardancy-imparting agent and flame-retardant resin composition |
| JP2013107955A (en) * | 2011-11-18 | 2013-06-06 | Lealea Enterprise Co Ltd | Resin composition for producing construction material |
-
1990
- 1990-12-28 JP JP40943490A patent/JPH04249550A/en active Pending
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0814531A3 (en) * | 1993-03-30 | 2000-02-16 | Canon Kabushiki Kaisha | Secondary battery |
| JPH11255955A (en) * | 1998-03-10 | 1999-09-21 | Hitachi Ltd | Capsule type flame retardant and resin composition for encapsulating semiconductor containing the same |
| US7828995B2 (en) * | 2003-10-02 | 2010-11-09 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Composition for a fire-protection agent for materials and fire-protection method |
| JP2006328345A (en) * | 2005-04-27 | 2006-12-07 | Hitachi Chem Co Ltd | Flame retardancy-imparting agent and flame-retardant resin composition |
| JP2012036398A (en) * | 2005-04-27 | 2012-02-23 | Hitachi Chem Co Ltd | Flame retardancy-imparting agent and flame-retardant resin composition |
| WO2008062820A1 (en) * | 2006-11-21 | 2008-05-29 | Autonetworks Technologies, Ltd. | Flame retardant, flame retardant composition, insulated wire, wiring harness, and method for producing flame retardant composition |
| US8933334B2 (en) | 2006-11-21 | 2015-01-13 | Autonetworks Technologies, Ltd. | Flame retardant, a flame-retardant composition, an insulated wire, a wiring harness, and a method for manufacturing the flame-retardant composition |
| JP2013107955A (en) * | 2011-11-18 | 2013-06-06 | Lealea Enterprise Co Ltd | Resin composition for producing construction material |
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