JPH07115863B2 - Zinc borate - Google Patents
Zinc borateInfo
- Publication number
- JPH07115863B2 JPH07115863B2 JP21924588A JP21924588A JPH07115863B2 JP H07115863 B2 JPH07115863 B2 JP H07115863B2 JP 21924588 A JP21924588 A JP 21924588A JP 21924588 A JP21924588 A JP 21924588A JP H07115863 B2 JPH07115863 B2 JP H07115863B2
- Authority
- JP
- Japan
- Prior art keywords
- zinc borate
- dipentaerythritol
- minutes
- acid
- mixed
- 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.)
- Expired - Lifetime
Links
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 title claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 9
- 150000005846 sugar alcohols Polymers 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 7
- 239000004593 Epoxy Substances 0.000 claims description 4
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims description 4
- 229960001545 hydrotalcite Drugs 0.000 claims description 2
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 13
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 13
- 239000003549 soybean oil Substances 0.000 description 8
- 235000012424 soybean oil Nutrition 0.000 description 8
- 229920003002 synthetic resin Polymers 0.000 description 7
- 239000000057 synthetic resin Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- -1 hydrotalcite compound Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- 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 description 1
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- YJLUBHOZZTYQIP-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=N2 YJLUBHOZZTYQIP-UHFFFAOYSA-N 0.000 description 1
- PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000010303 mechanochemical reaction Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229940079889 pyrrolidonecarboxylic acid Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 本発明はホウ酸亜鉛に関し、更に詳しくは合成樹脂に配
合した時の難燃性および熱安定性に優れたホウ酸亜鉛に
関する。The present invention relates to zinc borate, and more particularly to zinc borate having excellent flame retardancy and thermal stability when blended with a synthetic resin.
近年、合成樹脂製の建材や内装材あるいは電線などにお
いては難燃性の要求が著しい。難燃剤としてはハロゲン
化合物・アンチモン化合物が多用されているが、最近で
は合成樹脂の難燃時の溶融滴下をも防止する難燃剤とし
てホウ酸亜鉛が注目されてきている。しかしながらホウ
酸亜鉛を合成樹脂に配合した場合には、その成型加工時
において熱安定性の低下をもたらし、特に塩化ビニル樹
脂等のハロゲンを含有する樹脂においては、亜鉛バーニ
ングと呼ばれる如く、その低下が著しい。In recent years, there has been a great demand for flame retardancy in building materials and interior materials made of synthetic resins, electric wires and the like. Although halogen compounds and antimony compounds are frequently used as flame retardants, zinc borate has recently been attracting attention as a flame retardant that also prevents molten dripping of synthetic resins during flame retardation. However, when zinc borate is blended with a synthetic resin, it causes a decrease in thermal stability during the molding process, and particularly in a resin containing a halogen such as a vinyl chloride resin, such a decrease is caused as called zinc burning. Remarkable.
本発明者らはホウ酸亜鉛のもつ難燃性を維持しながら熱
安定性の低下を防止する方策として、ホウ酸亜鉛をハイ
ドロタルサイト類化合物・多価アルコール又は多価アル
コール部分エステル・エポキシ化合物のそれぞれ単独で
処理することをすでに見出しているが、今回これらの化
合物の２種以上を併用することにより、更に熱安定性の
改良に効果のあることを見出し本発明を完成するに至っ
た。The inventors of the present invention use zinc borate as a measure for preventing a decrease in thermal stability while maintaining the flame retardancy of zinc borate, by using hydrotalcite compounds, polyhydric alcohols or polyhydric alcohol partial esters, epoxy compounds. It has already been found that each of these compounds can be treated alone, but this time, it was found that the combined use of two or more of these compounds is effective in further improving the thermal stability, and the present invention has been completed.
すなわち本発明は、（１） ハイドロタルサイト類化合
物 （２） 多価アルコール又は多価アルコール部分エ
ステル （３） エポキシ化合物より選ばれた２種以上
で処理したことを特徴とするホウ酸亜鉛を提供するもの
である。That is, the present invention provides a zinc borate characterized by being treated with two or more selected from (1) hydrotalcite compounds (2) polyhydric alcohol or polyhydric alcohol partial ester (3) epoxy compound. To do.
本発明で使用するホウ酸亜鉛としては特に限定されるも
のではないが、合成樹脂への分散性や難燃性を考慮すれ
ば、平均粒径が20μｍ以下のものが好ましい。The zinc borate used in the present invention is not particularly limited, but in view of dispersibility in a synthetic resin and flame retardancy, an average particle size of 20 μm or less is preferable.
又、本発明で用いられるハイドロタルサイト類化合物と
しては、、組成式としてはMg6Al2（OH）16CO3・4H2O,Mg
4.5Al2（OH）13CO3・3.5H2O,Mg0.66Al0.34（OH）２（Si
O3）0.17・0.52H2O,Mg0.7Al0.3（OH）２（CO3）0.15・
0.55H2O等、商品名としては、協和化学工業（株）のア
ルカマイザー１、アルカマイザー２、アルカマイザー
３、アルカマイザー４、DHT−4A、キョーワード1000等
が挙げられる。The hydrotalcite compound used in the present invention has a composition formula of Mg 6 Al 2 (OH) 16 CO 3 .4H 2 O, Mg
4.5 Al 2 (OH) 13 CO 3 · 3.5H 2 O, Mg 0.66 Al 0.34 (OH) 2 (Si
O 3 ) 0.17・ 0.52H 2 O, Mg 0.7 Al 0.3 (OH) 2 (CO 3 ) 0.15・
Examples of trade names such as 0.55H 2 O include Alkamizer 1, Alkamizer 2, Alkamizer 3, Alkamizer 4, DHT-4A, and Kyoward 1000 manufactured by Kyowa Chemical Industry Co., Ltd.
又、本発明で用いられる多価アルコールおよび多価アル
コール部分エステルを構成する多価アルコールとして
は、ペンタエリスリトール・ジペンタエリスリトール・
トリペンタエリスリトール・ジグリセリン・ポリグリセ
リン・マンニトール・ソルビトール・トリスヒドロキシ
エチルイソシアヌレート・トリメチロールプロパン等が
挙げられ、同じく構成するカルボン酸としては、酢酸・
ラウリン酸・ステアリン酸・マレイン酸・フマル酸・ア
ジピン酸・フタル酸・トリメリット酸・安息香酸・酒石
酸・シュウ酸・リンゴ酸・マロン酸・ピロリドンカルボ
ン酸等が挙げられる。これらの具体的な例としては、ジ
ペンタエリスリトール・ジペンタエリスリトールモノア
セテート・ジペンタエリスリトールモノステアレート・
ジペンタエリスリトールアジピン酸エステル等である。The polyhydric alcohol and the polyhydric alcohol constituting the polyhydric alcohol partial ester used in the present invention include pentaerythritol, dipentaerythritol,
Examples include tripentaerythritol, diglycerin, polyglycerin, mannitol, sorbitol, trishydroxyethyl isocyanurate, trimethylolpropane, and the like.
Examples include lauric acid, stearic acid, maleic acid, fumaric acid, adipic acid, phthalic acid, trimellitic acid, benzoic acid, tartaric acid, oxalic acid, malic acid, malonic acid, pyrrolidonecarboxylic acid. Specific examples of these include dipentaerythritol / dipentaerythritol monoacetate / dipentaerythritol monostearate /
Examples thereof include dipentaerythritol adipate.
又、本発明で用いられるエポキシ化合物としては、エポ
キシ化大豆油、エポキシ化アマニ油、エポキシ化ヒマシ
油、エポキシ化ステアリン酸、エポキシ化ステアリン酸
メチル、エポキシ化ポリブタジエン、ビスフェノールＡ
−エピクロルヒドリン縮合物、クレゾールノボラック型
エポキシ樹脂等が挙げられる。Examples of the epoxy compound used in the present invention include epoxidized soybean oil, epoxidized linseed oil, epoxidized castor oil, epoxidized stearic acid, epoxidized methyl stearate, epoxidized polybutadiene, and bisphenol A.
-Epichlorohydrin condensate, cresol novolac type epoxy resin, etc. may be mentioned.
これらの化合物はホウ酸亜鉛に対して、それぞれ１〜20
重量％の範囲で、又合計量も１〜20重量％使用するのが
好ましく、１重量％未満では所望の熱安定性が得られ
ず、20重量％を越えると難燃性の低下をもたらす。These compounds are 1 to 20 each for zinc borate.
It is preferable to use 1 to 20% by weight in the range of weight% and the total amount is less than 1% by weight, the desired thermal stability cannot be obtained, and if it exceeds 20% by weight, the flame retardancy is lowered.
又、これらの化合物によるホウ酸亜鉛の処理方法である
が、Ｖブレンダーやリボンブレンダー等による単純な混
合処理では、合成樹脂にそれぞれ単独に配合した場合と
同じで効果は少ないが、ヘンシェルミキサー・スーパー
ミキサー・ローラーミル・ボールミル等による、メカノ
ケミカル的反応を生ずるような摩砕条件下で混合処理が
行なわれると、熱安定性の向上が著しい。Also, regarding the method for treating zinc borate with these compounds, a simple mixing treatment with a V blender, a ribbon blender, etc. is the same as when blended individually with a synthetic resin, but the effect is less, but Henschel Mixer Super When the mixing treatment is carried out by a mixer, roller mill, ball mill or the like under a milling condition that causes a mechanochemical reaction, the thermal stability is remarkably improved.
以下実施例により具体的に説明する。The present invention will be specifically described below with reference to examples.
比較例 １ 堺化学工業（株）製 未処理ホウ酸亜鉛（商品名:HA−
１）1kgとアルカマイザー150gをスーパーミキサーで10
分間混合し試料No.1を得た。Comparative Example 1 Untreated zinc borate (trade name: HA-, manufactured by Sakai Chemical Industry Co., Ltd.)
1) 10kg of 1kg and 150g of Alcamizer with a super mixer
Mixing for minutes gave Sample No. 1.
比較例 ２ HA−１ 1kgとジペンタエリスリトール50gをスーパーミ
キサーで10分間混合し試料No.2を得た。Comparative Example 2 HA-1 (1 kg) and dipentaerythritol (50 g) were mixed with a super mixer for 10 minutes to obtain sample No. 2.
比較例 ３ HA−１ 1kgとエポキシ化大豆油50gをスーパーミキサー
で10分間混合し試料No.3を得た。Comparative Example 3 HA-1 (1 kg) and epoxidized soybean oil (50 g) were mixed with a super mixer for 10 minutes to obtain sample No. 3.
比較例 ４ HA−１ 1kgとアルカマイザー１ 10g.ジペンタエリス
リトール20g、エポキシ化大豆油20gをＶブレンダーで30
分間混合し試料No.4を得た。Comparative Example 4 1 kg of HA-1 and 10 g of Alcamizer 1 20 g of dipentaerythritol and 20 g of epoxidized soybean oil were mixed with a V blender 30
Mixing for minutes gave Sample No. 4.
比較例 ５ HA−１ 1kgとアルカマイザー１ 1g、ジペンタエリス
リトール1g、エポキシ化大豆油1gをスーパーミキサーで
10分間混合し試料No.5を得た。Comparative Example 5 HA-1 (1 kg), Alkamizer 1 (1 g), Dipentaerythritol (1 g) and Epoxidized soybean oil (1 g) were mixed with a super mixer.
It mixed for 10 minutes and obtained sample No. 5.
比較例 ６ HA−１ 1kgとアルカマイザー１ 100g、ジペンタエリ
スリトール100g、エポキシ化大豆油100gをスーパーミキ
サーで10分間混合し試料No.6を得た。Comparative Example 6 HA-1 (1 kg), Alkamizer 1 (100 g), dipentaerythritol (100 g) and epoxidized soybean oil (100 g) were mixed with a super mixer for 10 minutes to obtain sample No. 6.
実施例 １ HA−１ 1kgとアルカマイザー１ 25g、ジペンタエリス
リトール25gをスーパーミキサーで10分間混合し試料No.
7を得た。Example 1 HA-1 (1 kg), Alkamizer 1 (25 g) and dipentaerythritol (25 g) were mixed with a super mixer for 10 minutes to prepare a sample No.
Got 7.
実施例 ２ HA−１ 1kgとジペンタエリスリトール25g、エポキシ化
大豆油25gをスーパーミキサーで10分間混合し試料No.8
を得た。Example 2 HA-1 (1 kg), dipentaerythritol (25 g), and epoxidized soybean oil (25 g) were mixed with a supermixer for 10 minutes to prepare sample No. 8
Got
実施例 ３ HA−１ 1kgとエポキシ化大豆油25g、アルカマイザー１
25gをスーパーミキサーで10分間混合し試料No.9を得
た。Example 3 HA-1 1 kg, epoxidized soybean oil 25 g, Alcamizer 1
25 g was mixed with a super mixer for 10 minutes to obtain sample No. 9.
実施例 ４ HA−１ 1kgとアルカマイザー１ 10g、ジペンタエリス
リトール20g、エポキシ化大豆油20gをスーパーミキサー
で10分間混合し試料No.10を得た。Example 4 HA-1 (1 kg), Alkamizer 1 (10 g), dipentaerythritol (20 g) and epoxidized soybean oil (20 g) were mixed with a super mixer for 10 minutes to obtain sample No. 10.
実施例 ５ HA−１ 1kgとアルカマイザー２ 20g、味の素（株）製
プレンライザーST−210（ジペンタエリスリトールアジ
ピン酸エステル）20g、東都化成（株）製エポトートYD
−128（ビスフェノールＡ−エピクロルヒドリン縮合型
エポキシ樹脂）10gをスーパーミキサーで10分間混合し
試料No.11を得た。Example 5 HA-1 1 kg and Alcamizer 2 20 g, Ajinomoto Co., Inc. Planerizer ST-210 (dipentaerythritol adipate) 20 g, Toto Kasei Co., Ltd. Epotote YD
Sample No. 11 was obtained by mixing 10 g of -128 (bisphenol A-epichlorohydrin condensation type epoxy resin) with a super mixer for 10 minutes.
実施例 ６ HA−１ 1kgとアルカマイザー１ 30g、プレンライザー
ST−210 40g、エポトートYD−128 30gをスーパーミキ
サーで10分間混合し試料No.12を得た。Example 6 1 kg of HA-1 and 30 g of Alcamizer 1 and Planerizer
40 g of ST-210 and 30 g of Epotote YD-128 were mixed with a super mixer for 10 minutes to obtain sample No.12.
上記のようにして得られた各試料を用いて、合成樹脂に
配合した場合の熱安定性および難燃性のテストを行なっ
た結果を第１表に示した。なお熱安定性は200℃のオー
ブン中における黒化（炭化）時間で評価し、難燃性は酸
素指数で評価した。Each sample obtained as described above was used to test the thermal stability and flame retardancy when compounded in a synthetic resin. The results are shown in Table 1. The thermal stability was evaluated by the blackening (carbonization) time in an oven at 200 ° C, and the flame retardancy was evaluated by the oxygen index.
Claims (1)
（２） 多価アルコール又は多価アルコール部分エステ
ル （３） エポキシ化合物より選ばれた２種以上で処
理したことを特徴とするホウ酸亜鉛。1. A hydrotalcite-based compound (1)
(2) Polyhydric alcohol or polyhydric alcohol partial ester (3) Zinc borate characterized by being treated with two or more selected from epoxy compounds.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21924588A JPH07115863B2 (en) | 1988-08-31 | 1988-08-31 | Zinc borate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21924588A JPH07115863B2 (en) | 1988-08-31 | 1988-08-31 | Zinc borate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0269314A JPH0269314A (en) | 1990-03-08 |
| JPH07115863B2 true JPH07115863B2 (en) | 1995-12-13 |
Family
ID=16732496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21924588A Expired - Lifetime JPH07115863B2 (en) | 1988-08-31 | 1988-08-31 | Zinc borate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07115863B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004291624A (en) * | 2003-03-13 | 2004-10-21 | Matsushita Electric Ind Co Ltd | Support structure of optical scanning device and image forming apparatus |
| DE102008024672A1 (en) | 2008-05-21 | 2009-11-26 | Bayer Materialscience Ag | Low-temperature polycarbonate blends |
| HUE047680T2 (en) * | 2013-11-28 | 2020-05-28 | Lanxess Deutschland Gmbh | Polyamide compositions |
-
1988
- 1988-08-31 JP JP21924588A patent/JPH07115863B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0269314A (en) | 1990-03-08 |
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