JPH04337343A - Flame-retardant resin composition - Google Patents
Flame-retardant resin compositionInfo
- Publication number
- JPH04337343A JPH04337343A JP13849991A JP13849991A JPH04337343A JP H04337343 A JPH04337343 A JP H04337343A JP 13849991 A JP13849991 A JP 13849991A JP 13849991 A JP13849991 A JP 13849991A JP H04337343 A JPH04337343 A JP H04337343A
- Authority
- JP
- Japan
- Prior art keywords
- flame
- retardant
- flame retardant
- resin composition
- comparative example
- 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.)
- Withdrawn
Links
- 239000003063 flame retardant Substances 0.000 title claims abstract description 105
- 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 90
- 239000011342 resin composition Substances 0.000 title claims abstract description 48
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 21
- 239000004793 Polystyrene Substances 0.000 claims abstract description 17
- 229920002223 polystyrene Polymers 0.000 claims abstract description 17
- 229910000410 antimony oxide Inorganic materials 0.000 claims abstract description 16
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims abstract description 16
- 230000000704 physical effect Effects 0.000 abstract description 16
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 abstract description 11
- 229920001903 high density polyethylene Polymers 0.000 abstract description 9
- 239000004700 high-density polyethylene Substances 0.000 abstract description 9
- DYIZJUDNMOIZQO-UHFFFAOYSA-N 4,5,6,7-tetrabromo-2-[2-(4,5,6,7-tetrabromo-1,3-dioxoisoindol-2-yl)ethyl]isoindole-1,3-dione Chemical compound O=C1C(C(=C(Br)C(Br)=C2Br)Br)=C2C(=O)N1CCN1C(=O)C2=C(Br)C(Br)=C(Br)C(Br)=C2C1=O DYIZJUDNMOIZQO-UHFFFAOYSA-N 0.000 abstract description 3
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 abstract description 3
- 229910052794 bromium Inorganic materials 0.000 abstract description 2
- 125000001246 bromo group Chemical group Br* 0.000 abstract description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 45
- 239000006185 dispersion Substances 0.000 description 21
- 238000002156 mixing Methods 0.000 description 17
- -1 polypropylene Polymers 0.000 description 17
- 238000002485 combustion reaction Methods 0.000 description 15
- 241000519995 Stachys sylvatica Species 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 239000002994 raw material Substances 0.000 description 10
- 239000004743 Polypropylene Substances 0.000 description 9
- 229920001155 polypropylene Polymers 0.000 description 9
- 238000005452 bending Methods 0.000 description 7
- 238000009863 impact test Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 238000009864 tensile test Methods 0.000 description 6
- 239000000654 additive Substances 0.000 description 4
- WUOBERCRSABHOT-UHFFFAOYSA-N diantimony Chemical compound [Sb]#[Sb] WUOBERCRSABHOT-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- AHBGXHAWSHTPOM-UHFFFAOYSA-N 1,3,2$l^{4},4$l^{4}-dioxadistibetane 2,4-dioxide Chemical compound O=[Sb]O[Sb](=O)=O AHBGXHAWSHTPOM-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000156978 Erebia Species 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229910017966 Sb2 O5 Inorganic materials 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229910000411 antimony tetroxide Inorganic materials 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical class N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- YEAUATLBSVJFOY-UHFFFAOYSA-N tetraantimony hexaoxide Chemical compound O1[Sb](O2)O[Sb]3O[Sb]1O[Sb]2O3 YEAUATLBSVJFOY-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
Landscapes
- Fireproofing Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、難燃性樹脂組成物に関
し、例えば家電製品、自動車部品、工業用部品等に利用
できる。FIELD OF INDUSTRIAL APPLICATION The present invention relates to a flame-retardant resin composition, which can be used, for example, in home appliances, automobile parts, industrial parts, and the like.
【0002】0002
【背景技術】ポリプロピレン(PP)、高密度ポリエチ
レン(HDPE)等のポリオレフィンは、強度、加工性
、価格等の点で優れているため、容器、フィルム等の一
般的な用途としてのみならず、工業用素材としても幅広
く用いられている。このようなポリオレフィンには、使
用目的によって難燃性が要求されることもある。そこで
、従来、難燃性を高めるようにした各種の樹脂組成物が
提案されている。例えば、特開昭50−9645号公報
によれば、難燃剤としてのハロゲン置換ジイミド化合物
の1種以上を含有する難燃性熱可塑性樹脂組成物の構成
が開示されている。[Background Art] Polyolefins such as polypropylene (PP) and high-density polyethylene (HDPE) are excellent in terms of strength, processability, price, etc., so they are not only used for general purposes such as containers and films, but also for industrial use. It is also widely used as a material. Such polyolefins may be required to have flame retardancy depending on the intended use. Therefore, various resin compositions with enhanced flame retardancy have been proposed. For example, JP-A-50-9645 discloses the structure of a flame-retardant thermoplastic resin composition containing one or more halogen-substituted diimide compounds as a flame retardant.
【0003】0003
【発明が解決しようとする課題】上記特開昭50−96
45号公報に係る樹脂組成物は、ハロゲン置換ジイミド
化合物の分散性が不良であるため、難燃性が不安定であ
る。従って、良好な難燃性を得るには添加量を増やす必
要があり、これにより混練時にメッシュ詰まりが発生し
たりして生産性の不安定を招いていた。また、この樹脂
組成物より成るペレットを射出成形したり、シートに成
形したものは難燃剤の白点が目立ち、外観が不良であっ
た。[Problem to be solved by the invention] The above-mentioned Japanese Patent Application Laid-Open No. 1983-1996
The resin composition according to Publication No. 45 has unstable flame retardancy because the halogen-substituted diimide compound has poor dispersibility. Therefore, in order to obtain good flame retardancy, it is necessary to increase the amount added, which causes mesh clogging during kneading, leading to instability in productivity. In addition, when pellets made of this resin composition were injection molded or formed into sheets, white spots from the flame retardant were noticeable and the appearance was poor.
【0004】なお、このような欠点を改良するため、ゴ
ム又はゴム弾性を有する樹脂を添加したり、例えばPP
とHDPE60〜40wt%に対して難燃剤と難燃助剤
を40〜60wt%添加するマスターバッチ化によるこ
とも提案されているが、依然として難燃剤の満足すべき
分散性が得られず、また難燃性も不安定である。そこで
、本発明は、難燃剤の良好な分散性が得られ、これによ
り優れた難燃性を有し、また優れた物性を備えながら、
難燃助剤も含めた難燃剤の添加量を少なくすることがで
きる難燃性樹脂組成物を提供することを目的とする。[0004] In order to improve these drawbacks, rubber or a resin having rubber elasticity may be added, for example, PP.
It has also been proposed to create a master batch by adding 40 to 60 wt% of a flame retardant and a flame retardant aid to 60 to 40 wt% of HDPE, but it is still not possible to obtain satisfactory dispersibility of the flame retardant, and Flammability is also unstable. Therefore, the present invention provides good dispersibility of the flame retardant, thereby having excellent flame retardancy, and having excellent physical properties.
It is an object of the present invention to provide a flame-retardant resin composition in which the amount of flame retardant including flame retardant aid can be reduced.
【0005】[0005]
【課題を解決するための手段及び作用】本発明に係る難
燃性樹脂組成物は、下記A、B、C成分を含有すること
を特徴とする。
A:ポリオレフィン系樹脂 70〜96wt
%B:下記a、bを含む難燃剤 20〜
3wt%[Means and effects for solving the problems] The flame-retardant resin composition according to the present invention is characterized by containing the following components A, B, and C. A: Polyolefin resin 70-96wt
%B: Flame retardant containing the following a and b 20~
3wt%
【化1】
b:臭素化ポリスチレン
C:アンチモン酸化物 10〜1w
t%但し、A+B+C=100wt%[Chemical formula 1] b: Brominated polystyrene C: Antimony oxide 10-1w
t% However, A+B+C=100wt%
【0006】本発明において使用する前記ポリオレフィ
ン系樹脂(A)としては、特に限定はなく、用途に応じ
て適宜なものを選ぶことができる。例えば、PP、HD
PE、低密度ポリエチレン(LDPE)、直鎖状低密度
ポリエチレン(LLDPE)等を挙げることができる。
また、これらの混合物を使用してもよい。このポリオレ
フィン系樹脂の含有割合が前記70wt%未満では物性
、特に伸びの低下が顕著になり、また前記96wt%を
越えると難燃性の低下が顕著になる。[0006] The polyolefin resin (A) used in the present invention is not particularly limited and can be appropriately selected depending on the intended use. For example, PP, HD
Examples include PE, low density polyethylene (LDPE), linear low density polyethylene (LLDPE), and the like. Also, mixtures of these may be used. If the content of the polyolefin resin is less than 70 wt%, the physical properties, especially elongation, will be significantly lowered, and if it exceeds 96 wt%, the flame retardancy will be significantly lowered.
【0007】前記難燃剤(B)中、化1で示されるハロ
ゲン化フタル酸イミド誘導体の具体例としては、次のよ
うな化合物が挙げられる。例えば、メチレンビス(テト
ラブロモフタル酸イミド)、エチレンビス(テトラブロ
モフタル酸イミド)、プロピレンビス(テトラブロモフ
タル酸イミド)、ブチレンビス(テトラブロモフタル酸
イミド)、ベンジジンビス(テトラブロモフタル酸イミ
ド)、メチレンビス(テトラクロロフタル酸イミド)、
エチレンビス(テトラクロロフタル酸イミド)、プロピ
レンビス(テトラクロロフタル酸イミド)、ブチレンビ
ス(テトラクロロフタル酸イミド)等があり、これらの
中で特にエチレンビス(テトラブロモフタル酸イミド)
が好ましい。前記難燃剤(B)中の臭素化ポリスチレン
は、その重合度と臭素含量について特に限定はないが、
スチレン単位当たり3個以上の臭素を有するものが好ま
しい。In the flame retardant (B), specific examples of the halogenated phthalimide derivative represented by Chemical Formula 1 include the following compounds. For example, methylene bis (tetrabromophthalic acid imide), ethylene bis (tetrabromophthalic acid imide), propylene bis (tetrabromophthalic acid imide), butylene bis (tetrabromophthalic acid imide), benzidine bis (tetrabromophthalic acid imide), Methylenebis(tetrachlorophthalimide),
There are ethylene bis (tetrachlorophthalic acid imide), propylene bis (tetrachlorophthalic acid imide), butylene bis (tetrachlorophthalic acid imide), etc. Among these, ethylene bis (tetrabromophthalic acid imide) is particularly
is preferred. The degree of polymerization and bromine content of the brominated polystyrene in the flame retardant (B) are not particularly limited;
Those having three or more bromines per styrene unit are preferred.
【0008】これらのa、bを含む難燃剤(B)の含有
割合が前記3wt%未満では難燃性が低下し、また前記
20wt%を越えて添加しても難燃性の向上が認められ
ず、コストアップとなる。また、難燃剤(B)中のa、
bの含有割合は、a/b=30〜70/70〜30(重
量比)とするが、この範囲を外れると、充分な難燃性が
得られなくなる。前記アンチモン酸化物(C)は難燃助
剤として作用するものであり、この具体例としては、三
酸化二アンチモン(Sb2 O3 )、四酸化二アンチ
モン(Sb2 O4 )、五酸化二アンチモン(Sb2
O5 )等がある。これらの中で、特に三酸化二アン
チモンが好ましい。このアンチモン酸化物(C)の含有
割合が前記1wt%未満では難燃性が低下し、また前記
10wt%を越えると物性、特に引張り伸び率の低下が
顕著になる。難燃剤(B)とアンチモン酸化物(C)の
含有割合は、B/C=2〜4/1(重量比)とするが、
この範囲を外れると、充分な難燃性が得られなくなる。[0008] If the content of the flame retardant (B) containing these a and b is less than 3 wt%, the flame retardancy decreases, and even if it is added in excess of 20 wt%, an improvement in flame retardancy is observed. This will increase costs. In addition, a in the flame retardant (B),
The content ratio of b is set to a/b=30 to 70/70 to 30 (weight ratio), but if it is out of this range, sufficient flame retardance will not be obtained. The antimony oxide (C) acts as a flame retardant aid, and specific examples thereof include diantimony trioxide (Sb2O3), diantimony tetroxide (Sb2O4), diantimony pentoxide (Sb2
O5) etc. Among these, diantimony trioxide is particularly preferred. If the content of antimony oxide (C) is less than 1 wt%, the flame retardancy will be lowered, and if it exceeds 10 wt%, the physical properties, especially the tensile elongation rate, will be significantly lowered. The content ratio of the flame retardant (B) and antimony oxide (C) is B/C = 2 to 4/1 (weight ratio),
Outside this range, sufficient flame retardancy cannot be obtained.
【0009】本発明の難燃性樹脂組成物中には、上記A
、B、C以外に各種の添加剤や充填剤を添加してもよい
。例えば、添加剤としては、酸化防止剤、滑剤、紫外線
吸収剤、安定剤、顔料等の樹脂成形品において通常添加
されるものがあり、これらを適宜使用することができる
。また、充填剤としては、タルク、炭酸カルシウム、沈
降性硫酸バリウム等を適宜使用することができる。なお
、本発明の難燃性樹脂組成物を製造する際の原料の混合
、混練方法は任意である。例えば、下記実施例記載の方
法の他に、ポリオレフィン系樹脂(A)、難燃剤(B)
、アンチモン酸化物(C)を混合、混練してマスターバ
ッチを調製し、これにポリオレフィン系樹脂(A)を前
記マスターバッチに対して5〜15倍量配合して最終的
に本発明に係る樹脂組成物を製造するようにしてもよい
。The flame retardant resin composition of the present invention contains the above-mentioned A
, B, and C, various additives and fillers may be added. For example, additives include those commonly added to resin molded products, such as antioxidants, lubricants, ultraviolet absorbers, stabilizers, and pigments, and these can be used as appropriate. Further, as the filler, talc, calcium carbonate, precipitated barium sulfate, etc. can be used as appropriate. In addition, the mixing and kneading methods of raw materials when producing the flame-retardant resin composition of the present invention are arbitrary. For example, in addition to the methods described in the examples below, polyolefin resin (A), flame retardant (B)
, antimony oxide (C) are mixed and kneaded to prepare a masterbatch, and a polyolefin resin (A) is blended therein in an amount of 5 to 15 times the amount of the masterbatch to finally produce the resin according to the present invention. A composition may also be manufactured.
【0010】0010
【実施例】実施例1〜5
先ず、下記の原料を表1に示す配合割合で混合して各実
施例に係る難燃性樹脂組成物より成る樹脂ペレットを得
た。ここで使用した混練機は、池貝鉄工(株)製のワー
ナータイプPCM45mm2軸混練機である。スクリュ
ーの回転数は150rpm 、また成形時のシリンダー
温度は、ホッパー側からダイス側に230℃、250℃
、230℃、220℃、220℃、(ダイス)220℃
の分布を有していた。各実施例に係る樹脂組成物の密度
とメルトインデックス(MI)は、表1に示す通りであ
る。
なお、このMIは、HDPE系樹脂については190℃
、荷重2160gの条件で測定し、またHDPE/PP
系とPP系樹脂については230℃、荷重2160gの
条件で測定した。なお、表中、各原料の配合量でポリオ
レフィン系樹脂、難燃剤及び難燃助剤はwt%を示し、
分散剤と酸化防止剤は前記3者の合計を100 重量部
とした場合の重量部を示す。Examples Examples 1 to 5 First, the following raw materials were mixed in the proportions shown in Table 1 to obtain resin pellets comprising the flame retardant resin compositions according to each example. The kneader used here is a Warner type PCM 45 mm twin-screw kneader manufactured by Ikegai Tekko Co., Ltd. The rotation speed of the screw is 150 rpm, and the cylinder temperature during molding is 230°C and 250°C from the hopper side to the die side.
, 230℃, 220℃, 220℃, (Dice) 220℃
distribution. The density and melt index (MI) of the resin composition according to each example are shown in Table 1. Note that this MI is 190°C for HDPE resin.
, measured under the condition of load 2160g, and HDPE/PP
The system and PP resin were measured under the conditions of 230° C. and a load of 2160 g. In addition, in the table, polyolefin resin, flame retardant, and flame retardant aid are shown in wt% in the blending amount of each raw material,
The parts by weight of the dispersant and antioxidant are based on the total of the above three parts being 100 parts by weight.
【0011】
ポリオレフィン系樹脂……HDPE(MI=0.25)
化1のハロゲン化フタル酸イミド誘導体……下記の化2
に示すサイテックスBT−93〔商品名、エチル・コー
ポレーション製、物質名:1,2−ビス(テトラブロモ
フタルイミド)エタン〕Polyolefin resin...HDPE (MI=0.25)
Halogenated phthalic acid imide derivative of chemical formula 1...the following chemical compound 2
Cytex BT-93 (trade name, manufactured by Ethyl Corporation, substance name: 1,2-bis(tetrabromophthalimide)ethane) shown in
【化2】
臭素化ポリスチレン……下記の化3に示すパイロチェッ
ク68PB〔商品名、日産フェロ有機化学(株)製〕[Chemical formula 2] Brominated polystyrene...Pyrocheck 68PB shown in Chemical formula 3 below [trade name, manufactured by Nissan Ferro Organic Chemical Co., Ltd.]
【
化3】[
Chemical 3]
【0012】
アンチモン酸化物……三酸化二アンチモン(Sb2 O
3 )
分散剤……カデナックスGS90〔商品名、ライオン(
株)製、物質名:グリセリンモノステアレート〕及びレ
オスタットT−60〔商品名、ライオン(株)製、物質
名:ソルビタンモノステアレート〕
酸化防止剤……マーク2112〔商品名、アデカ・アー
ガス(株)製、物質名:トリス(2,4ジt−ブチルフ
ェニル)ホスファイト〕及びマークAO−60〔商品名
、旭電化(株)製、物質名:テトラキス−[メチレン−
3−(3′,5′−ジ−ターシャリ−ブチル−4′−ヒ
ドロキシフェニル)プロピオネート]メタンAntimony oxide...Diantimony trioxide (Sb2O
3) Dispersant... Cadenax GS90 [Product name, Lion (
Co., Ltd., substance name: Glycerin Monostearate] and Rheostat T-60 [Product name, Lion Co., Ltd., substance name: Sorbitan Monostearate] Antioxidant...Mark 2112 [Product name, Adeca Argus ( manufactured by Asahi Denka Co., Ltd., substance name: tris(2,4 di-t-butylphenyl) phosphite] and mark AO-60 [trade name, manufactured by Asahi Denka Co., Ltd., substance name: tetrakis-[methylene-
3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)propionate]methane
【0013
】次に、各実施例の樹脂組成物より成る試験片を作製し
て、引張り試験、曲げ試験及びアイゾット(IZOD)
衝撃試験をそれぞれ行った。前記引張り試験は、AST
M D638に準拠して、引張り強度、引張り弾性率
及び引張り伸び率について測定した。前記曲げ試験は、
ASTM D790に準拠して、曲げ強度と曲げ弾性
率について測定した。前記アイゾット衝撃試験は、AS
TMD256に準拠して、ノッチ付きとノッチ無しのも
のについて測定した。その結果を表1に示す。
表中、アイゾット衝撃試験の欄のNBは、ノンブレーク
(破壊せず)を意味する。0013
Next, test pieces made of the resin compositions of each example were prepared and subjected to a tensile test, a bending test, and an IZOD test.
An impact test was conducted on each. The tensile test is AST
Tensile strength, tensile modulus, and tensile elongation were measured in accordance with MD638. The bending test is
Bending strength and flexural modulus were measured in accordance with ASTM D790. The Izod impact test
In accordance with TMD256, measurements were made for those with and without a notch. The results are shown in Table 1. In the table, NB in the Izod impact test column means non-break (not destroyed).
【0014】次に、各実施例の樹脂ペレットを使用して
難燃剤の分散判定用のプレート(3.2 mm×80m
m×80mm)とフィルム(厚さ20〜50μm 、5
0mm×50mm)を成形した。プレート作製の際使用
した射出成形機は、日精樹脂工業(株)製のFS150
(商品名)である。成形時のシリンダー温度は、ホッパ
ー側からダイス側に190℃、200℃、210℃、(
ダイス)200℃の分布を有していた。フィルム作製の
際使用した成形機は、東邦機械工業(株)製の50t圧
縮成形機であり、ヒータ温度は200℃であった。また
、同じ樹脂ペレットを成形して燃焼試験用の厚さの異な
る2種類の試験片(3.2mm ×12.7mm×12
7mm 及び1.6mm ×12.7mm×127mm
)を作製した。使用した射出成形機は、日精樹脂工業
(株)製のFS50(商品名)である。成形時のシリン
ダー温度は、ホッパー側からダイス側に190℃、20
0℃、210℃、(ダイス)200℃の分布を有してい
た。Next, using the resin pellets of each example, a plate (3.2 mm x 80 m
m x 80 mm) and film (thickness 20-50 μm, 5
0 mm x 50 mm). The injection molding machine used for producing the plate was FS150 manufactured by Nissei Jushi Kogyo Co., Ltd.
(product name). The cylinder temperature during molding is 190℃, 200℃, 210℃, (
Dice) had a distribution of 200°C. The molding machine used for film production was a 50t compression molding machine manufactured by Toho Kikai Kogyo Co., Ltd., and the heater temperature was 200°C. In addition, two types of test pieces (3.2 mm x 12.7 mm x 12
7mm and 1.6mm x 12.7mm x 127mm
) was created. The injection molding machine used was FS50 (trade name) manufactured by Nissei Jushi Kogyo Co., Ltd. The cylinder temperature during molding is 190℃ and 20℃ from the hopper side to the die side.
It had a distribution of 0°C, 210°C, and (dice) 200°C.
【0015】次に、これらのプレートとフィルムを使用
して難燃剤の分散状態を判定し、また前記2種類の試験
片を使用して燃焼試験を行った。その結果を下記の表1
に示す。これらの分散判定方法及び燃焼試験方法は、下
記の通りである。
分散判定方法
(1)射出プレートを用いた分散判定は、プレートに直
径0.1 〜0.5mm の白点(難燃剤の分散不良に
よる凝集物)が幾つ見られるかを数えることにより行っ
た。
(2)プレスフィルムを用いた分散判定は、前記プレー
トの場合と同様にフィルム中に存在する白点の数を数え
ることにより行った。
これらの分散判定で、白点が0〜5個を○、6〜30個
を△、31個以上を×とした。
燃焼試験方法
この燃焼試験方法は、米国UL(Underwrite
rs Laboratories Inc.)の試験規
格である、UL94の垂直試験(V)に基づいて行った
。その燃焼性は、不良なものから良好なものに、HB、
V−2、V−1、V−0の4段階に分けて評価する。な
お、試験片の厚さが薄い程、相対的に燃えやすくなるの
で、条件としては厳しくなる。Next, the dispersion state of the flame retardant was determined using these plates and films, and a combustion test was conducted using the two types of test pieces. The results are shown in Table 1 below.
Shown below. These dispersion determination methods and combustion test methods are as follows. Dispersion Judgment Method (1) Dispersion judgment using an injection plate was performed by counting how many white spots (agglomerates due to poor dispersion of the flame retardant) with a diameter of 0.1 to 0.5 mm were observed on the plate. (2) Dispersion determination using a press film was performed by counting the number of white spots present in the film as in the case of the plate. In these dispersion evaluations, 0 to 5 white points were evaluated as ◯, 6 to 30 white points as △, and 31 or more white points as ×. Combustion test method This combustion test method is based on the U.S. UL (Underwrite)
rs Laboratories Inc. ) The test was conducted based on the UL94 vertical test (V). Its flammability ranges from poor to good: HB,
Evaluation is divided into four stages: V-2, V-1, and V-0. Note that the thinner the test piece is, the more easily it burns, so the conditions become stricter.
【表1】[Table 1]
【0016】比較例1〜4
上記実施例と同様にして各比較例に係る樹脂組成物につ
いて各種の物性試験を行い、また難燃剤の分散判定と燃
焼試験を行った。その結果を下記の表2に示す。但し、
表2に示すように、各比較例毎に使用した原料及び配合
割合を異ならせた。即ち、比較例1では、難燃剤のうち
、ハロゲン化フタル酸イミド誘導体のみを使用し、比較
例2では、臭素化ポリスチレンのみを使用した。また、
比較例3と4では、ポリオレフィン系樹脂、難燃剤及び
アンチモン酸化物のうちの少なくとも一つの配合量を本
発明に係る範囲外のものとした。Comparative Examples 1 to 4 In the same manner as in the above Examples, various physical property tests were conducted on the resin compositions of each Comparative Example, and flame retardant dispersion determination and combustion tests were also conducted. The results are shown in Table 2 below. however,
As shown in Table 2, the raw materials and blending ratios used were different for each comparative example. That is, in Comparative Example 1, only a halogenated phthalimide derivative was used among the flame retardants, and in Comparative Example 2, only brominated polystyrene was used. Also,
In Comparative Examples 3 and 4, the amount of at least one of the polyolefin resin, flame retardant, and antimony oxide was outside the range according to the present invention.
【表2】[Table 2]
【0017】実施例及び比較例の考察
上記実施例1〜5によれば、各実施例の難燃性樹脂組成
物より成る試験片は、それぞれ引張り試験、曲げ試験及
びアイゾット衝撃試験の結果が示すように良好な物性を
有している。また、各実施例に係る樹脂組成物より成る
プレートとフィルムは、難燃剤の分散判定において、難
燃剤の分散不良による凝集物を示す白点が殆ど見られず
、難燃剤がプレート中又はフィルム中に良好に分散して
いることがわかる。このようにプレート中又はフィルム
中に難燃剤が良好に分散しているため、各実施例に係る
樹脂組成物より成る2種類の試験片は、燃焼試験の結果
が示すように、それぞれ難燃性を有している。Discussion of Examples and Comparative Examples According to Examples 1 to 5 above, the test pieces made of the flame-retardant resin compositions of each example showed the results of the tensile test, bending test, and Izod impact test, respectively. It has good physical properties. In addition, in the dispersion evaluation of the flame retardant, the plates and films made of the resin compositions according to each example showed almost no white spots indicating aggregates due to poor dispersion of the flame retardant, indicating that the flame retardant was present in the plate or in the film. It can be seen that the particles are well dispersed. Because the flame retardant was well dispersed in the plate or film, the two types of test pieces made of the resin compositions according to each example showed flame retardant properties, as shown by the results of the combustion test. have.
【0018】これに対して、比較例1によれば、難燃剤
のうち、ハロゲン化フタル酸イミド誘導体のみを使用し
、臭素化ポリスチレンを添加していないため、この比較
例に係る樹脂組成物より成るプレートとフィルムは、そ
れぞれ白点が多数目立ち、難燃剤がプレート中又はフィ
ルム中に良好に分散していないことがわかる。また、引
張りの伸び率も低い。比較例2によれば、難燃剤のうち
、臭素化ポリスチレンのみを使用し、ハロゲン化フタル
酸イミド誘導体を添加していないため、この比較例に係
る樹脂組成物より成るプレートとフィルムは、それぞれ
白点が目立ち、難燃剤がプレート中又はフィルム中に良
好に分散していないことがわかる。比較例3によれば、
ポリオレフィン系樹脂の配合量が本発明に係る範囲より
多く、また難燃剤とアンチモン酸化物の配合量が本発明
に係る範囲より少ないため、難燃性が不良であった。比
較例4によれば、ポリオレフィン系樹脂の配合量が本発
明に係る範囲より少なく、またアンチモン酸化物の配合
量が本発明に係る範囲より多いため、分散判定と難燃性
は良好であっても、引張りの伸び率とアイゾット衝撃強
度に問題があった。On the other hand, according to Comparative Example 1, only a halogenated phthalic acid imide derivative was used among the flame retardants, and brominated polystyrene was not added. Both the plate and the film had many conspicuous white spots, indicating that the flame retardant was not well dispersed in the plate or film. Furthermore, the tensile elongation rate is low. According to Comparative Example 2, of the flame retardants, only brominated polystyrene was used and no halogenated phthalimide derivative was added, so the plate and film made of the resin composition according to this comparative example were white. The dots are noticeable, indicating that the flame retardant is not well dispersed in the plate or film. According to Comparative Example 3,
Since the blending amount of the polyolefin resin was higher than the range according to the present invention, and the blending amount of the flame retardant and antimony oxide was lower than the range according to the present invention, the flame retardance was poor. According to Comparative Example 4, the blending amount of the polyolefin resin was lower than the range according to the present invention, and the blending amount of antimony oxide was higher than the range according to the present invention, so the dispersion judgment and flame retardancy were good. However, there were problems with tensile elongation and Izod impact strength.
【0019】実施例6〜13
上記実施例1〜5と同様にして各実施例に係る難燃性樹
脂組成物を製造し、これらの樹脂組成物を使用して上記
実施例と同様の物性試験、難燃剤の分散判定及び燃焼試
験を行った。その結果を下記の表3,4に示す。但し、
表3,4に示すように、各実施例毎に使用した原料及び
配合割合を異ならせた。即ち、これらの実施例では、ポ
リオレフィン系樹脂としてPPとHDPEを使用した。Examples 6 to 13 Flame-retardant resin compositions according to each example were produced in the same manner as in Examples 1 to 5 above, and these resin compositions were subjected to physical property tests similar to those in the above Examples. , flame retardant dispersion determination and combustion test were conducted. The results are shown in Tables 3 and 4 below. however,
As shown in Tables 3 and 4, the raw materials and blending ratios used were different for each example. That is, in these Examples, PP and HDPE were used as the polyolefin resins.
【0020】比較例5〜7
上記実施例6〜13と同様にして各比較例に係る難燃性
樹脂組成物を製造し、これらの樹脂組成物を使用して上
記実施例と同様の物性試験、難燃剤の分散判定及び燃焼
試験を行った。その結果を下記の表4に示す。但し、表
4に示すように、各比較例毎に使用した原料及び配合割
合を異ならせた。即ち、比較例5では、難燃剤のうち、
ハロゲン化フタル酸イミド誘導体のみを使用し、比較例
6では、臭素化ポリスチレンのみを使用した。また、比
較例7では、ポリオレフィン系樹脂、難燃剤及びアンチ
モン酸化物のうちの少なくとも一つの配合量を本発明に
係る範囲外のものとした。Comparative Examples 5 to 7 Flame-retardant resin compositions according to each comparative example were produced in the same manner as in Examples 6 to 13 above, and these resin compositions were subjected to physical property tests similar to those in the above Examples. , flame retardant dispersion determination and combustion test were conducted. The results are shown in Table 4 below. However, as shown in Table 4, the raw materials and blending ratios used were different for each comparative example. That is, in Comparative Example 5, among the flame retardants,
Only halogenated phthalimide derivatives were used, and in Comparative Example 6, only brominated polystyrene was used. Furthermore, in Comparative Example 7, the amount of at least one of the polyolefin resin, flame retardant, and antimony oxide was outside the range according to the present invention.
【表3】[Table 3]
【表4】[Table 4]
【0021】実施例及び比較例の考察
上記実施例6〜13によれば、各実施例の難燃性樹脂組
成物より成る試験片は、それぞれ引張試験、曲げ試験及
びアイゾット衝撃試験の結果が示すように良好な物性を
有している。また、各実施例に係る樹脂組成物より成る
プレートとフィルムは、難燃剤の分散判定において、白
点が殆ど見られず、難燃剤がプレート中又はフィルム中
に良好に分散していることがわかる。このようにプレー
ト中又はフィルム中に難燃剤が良好に分散しているため
、各実施例に係る樹脂組成物より成る2種類の試験片は
、燃焼試験の結果が示すように、それぞれ難燃性を有し
ている。Discussion of Examples and Comparative Examples According to Examples 6 to 13 above, the test pieces made of the flame-retardant resin compositions of each example showed the results of the tensile test, bending test, and Izod impact test, respectively. It has good physical properties. In addition, in the plates and films made of the resin compositions according to each example, almost no white spots were observed in the flame retardant dispersion evaluation, indicating that the flame retardants were well dispersed in the plates or films. . Because the flame retardant was well dispersed in the plate or film, the two types of test pieces made of the resin compositions according to each example showed flame retardant properties, as shown by the results of the combustion test. have.
【0022】これに対して、比較例5によれば、難燃剤
のうち、ハロゲン化フタル酸イミド誘導体のみを使用し
、臭素化ポリスチレンを添加していないため、この比較
例に係る樹脂組成物より成るプレートとフィルムは、そ
れぞれ白点が多数目立ち、難燃剤がプレート中又はフィ
ルム中に良好に分散しておらず、難燃性も不良であるこ
とがわかる。比較例6によれば、難燃剤のうち、臭素化
ポリスチレンのみを使用し、ハロゲン化フタル酸イミド
誘導体を添加していないため、この比較例に係る樹脂組
成物より成るプレートとフィルムは、それぞれ白点が目
立ち、難燃剤がプレート中又はフィルム中に良好に分散
しておらず、難燃性も不良であることがわかる。比較例
7によれば、ポリオレフィン系樹脂とアンチモン酸化物
の配合量が本発明に係る範囲より少なく、また難燃剤の
配合量が本発明に係る範囲より多いため、分散判定と難
燃性は良好であっても、引張り伸び率と衝撃特性に問題
があった。On the other hand, according to Comparative Example 5, only a halogenated phthalic acid imide derivative was used among the flame retardants, and no brominated polystyrene was added, so that the resin composition according to this comparative example The resulting plate and film each had many conspicuous white spots, indicating that the flame retardant was not well dispersed in the plate or film, and the flame retardancy was also poor. According to Comparative Example 6, among the flame retardants, only brominated polystyrene was used and no halogenated phthalimide derivative was added, so the plate and film made of the resin composition according to this comparative example were white. The dots are conspicuous, indicating that the flame retardant is not well dispersed in the plate or film, and the flame retardancy is also poor. According to Comparative Example 7, the blending amount of the polyolefin resin and antimony oxide is lower than the range according to the present invention, and the blending amount of the flame retardant is higher than the range according to the present invention, so the dispersion judgment and flame retardancy are good. However, there were problems with tensile elongation and impact properties.
【0023】実施例14,15
上記実施例1〜5と同様にして各実施例に係る難燃性樹
脂組成物を製造し、これらの樹脂組成物を使用して上記
実施例と同様の物性試験、難燃剤の分散判定及び燃焼試
験を行った。その結果を下記の表5に示す。但し、表5
に示すように、各実施例毎に使用した原料及び配合割合
を異ならせた。即ち、これらの実施例では、ポリオレフ
ィン系樹脂としてPPを使用した。Examples 14 and 15 Flame-retardant resin compositions according to each example were produced in the same manner as in Examples 1 to 5 above, and the same physical property tests as in the above Examples were conducted using these resin compositions. , flame retardant dispersion determination and combustion test were conducted. The results are shown in Table 5 below. However, Table 5
As shown in , the raw materials used and the blending ratios were different for each example. That is, in these Examples, PP was used as the polyolefin resin.
【0024】比較例8〜10
上記実施例14,15と同様にして各比較例に係る難燃
性樹脂組成物を製造し、これらの樹脂組成物を使用して
上記実施例と同様の物性試験、難燃剤の分散判定及び燃
焼試験を行った。その結果を下記の表5に示す。但し、
表5に示すように、各比較例毎に使用した原料及び配合
割合を異ならせた。即ち、比較例8では、難燃剤のうち
、ハロゲン化フタル酸イミド誘導体のみを使用し、比較
例9では、臭素化ポリスチレンのみを使用した。また、
比較例10では、ポリオレフィン系樹脂、難燃剤及びア
ンチモン酸化物のうちの少なくとも一つの配合量を本発
明に係る範囲外のものとした。Comparative Examples 8 to 10 Flame-retardant resin compositions according to each comparative example were produced in the same manner as in Examples 14 and 15 above, and the same physical property tests as in the above Examples were conducted using these resin compositions. , flame retardant dispersion determination and combustion test were conducted. The results are shown in Table 5 below. however,
As shown in Table 5, the raw materials and blending ratios used were different for each comparative example. That is, in Comparative Example 8, only a halogenated phthalimide derivative was used among the flame retardants, and in Comparative Example 9, only brominated polystyrene was used. Also,
In Comparative Example 10, the amount of at least one of the polyolefin resin, flame retardant, and antimony oxide was outside the range according to the present invention.
【表5】[Table 5]
【0025】実施例及び比較例の考察
上記実施例14,15によれば、各実施例の難燃性樹脂
組成物より成る試験片は、それぞれ引張試験、曲げ試験
及びアイゾット衝撃試験の結果が示すように良好な物性
を有している。また、各実施例に係る樹脂組成物より成
るプレートとフィルムは、難燃剤の分散判定において、
白点が殆ど見られず、難燃剤がプレート中又はフィルム
中に良好に分散していることがわかる。このようにプレ
ート中又はフィルム中に難燃剤が良好に分散しているた
め、各実施例に係る樹脂組成物より成る2種類の試験片
は、燃焼試験の結果が示すように、それぞれ難燃性を有
している。Discussion of Examples and Comparative Examples According to Examples 14 and 15 above, the test pieces made of the flame-retardant resin compositions of each example showed the results of the tensile test, bending test, and Izod impact test, respectively. It has good physical properties. In addition, the plates and films made of the resin compositions according to each example were evaluated for dispersion of flame retardants.
Almost no white spots were observed, indicating that the flame retardant was well dispersed in the plate or film. Because the flame retardant was well dispersed in the plate or film, the two types of test pieces made of the resin compositions according to each example showed flame retardant properties, as shown by the results of the combustion test. have.
【0026】これに対して、比較例8によれば、難燃剤
のうち、ハロゲン化フタル酸イミド誘導体のみを使用し
、臭素化ポリスチレンを添加していないため、この比較
例に係る樹脂組成物より成るプレートとフィルムは、そ
れぞれ白点が多数目立ち、難燃剤がプレート中又はフィ
ルム中に良好に分散していないことがわかる。また、衝
撃特性も不良であった。比較例9によれば、難燃剤のう
ち、臭素化ポリスチレンのみを使用し、ハロゲン化フタ
ル酸イミド誘導体を添加していないため、この比較例に
係る樹脂組成物より成るプレートとフィルムは、それぞ
れ白点が目立ち、難燃剤がプレート中又はフィルム中に
良好に分散していないことがわかる。また、衝撃強度と
引張り伸び率も低い。比較例10によれば、ポリオレフ
ィン系樹脂の配合量が本発明に係る範囲より多く、また
難燃剤の配合量が本発明に係る範囲より少ないため、難
燃剤の分散が良好であっても、難燃性に問題があった。On the other hand, according to Comparative Example 8, only a halogenated phthalic acid imide derivative was used among the flame retardants, and brominated polystyrene was not added. Both the plate and the film had many conspicuous white spots, indicating that the flame retardant was not well dispersed in the plate or film. In addition, the impact properties were also poor. According to Comparative Example 9, of the flame retardants, only brominated polystyrene was used and no halogenated phthalimide derivative was added, so the plate and film made of the resin composition according to this comparative example were white. The dots are noticeable, indicating that the flame retardant is not well dispersed in the plate or film. It also has low impact strength and tensile elongation. According to Comparative Example 10, the blending amount of the polyolefin resin is higher than the range according to the present invention, and the blending amount of the flame retardant is lower than the range according to the present invention, so even if the flame retardant is well dispersed, the There was a problem with flammability.
【0027】実施例16
上記実施例1〜5と同様にして実施例16に係る難燃性
樹脂組成物を製造し、この樹脂組成物を使用して上記実
施例と同様の物性試験、難燃剤の分散判定及び燃焼試験
を行った。その結果を下記の表6に示す。但し、表6に
示すように、この実施例では使用した原料及び配合割合
を異ならせた。即ち、この実施例では、ポリオレフィン
系樹脂としてPPとHDPEを使用し、充填剤としてタ
ルクも使用した。なお、この表6で、タルクの配合量は
wt%を示す。また、この表においては、ポリオレフィ
ン系樹脂、難燃剤、難燃助剤及びタルクの合計を100
wt%とし、他の添加剤は前記4者の合計を100重量
部とした場合の重量部を示す。Example 16 A flame retardant resin composition according to Example 16 was produced in the same manner as in Examples 1 to 5 above, and this resin composition was used to perform physical property tests and flame retardant tests in the same manner as in the above Examples. Dispersion determination and combustion tests were conducted. The results are shown in Table 6 below. However, as shown in Table 6, in this example, the raw materials used and the blending ratio were different. That is, in this example, PP and HDPE were used as polyolefin resins, and talc was also used as a filler. In addition, in this Table 6, the amount of talc is expressed in wt%. In addition, in this table, the total of polyolefin resin, flame retardant, flame retardant aid, and talc is
% by weight, and other additives are shown in parts by weight when the total of the above four additives is 100 parts by weight.
【0028】比較例11,12
上記実施例16と同様にして各比較例に係る難燃性樹脂
組成物を製造し、これらの樹脂組成物を使用して上記実
施例と同様の物性試験、難燃剤の分散判定及び燃焼試験
を行った。その結果を下記の表6に示す。但し、表6に
示すように、各比較例毎に使用した原料及び配合割合を
異ならせた。即ち、比較例11では、難燃剤のうち、ハ
ロゲン化フタル酸イミド誘導体のみを使用し、比較例9
では、臭素化ポリスチレンのみを使用した。Comparative Examples 11 and 12 Flame-retardant resin compositions according to each comparative example were produced in the same manner as in Example 16 above, and these resin compositions were subjected to the same physical property tests and resistance tests as in the above Example. A fuel dispersion determination and a combustion test were conducted. The results are shown in Table 6 below. However, as shown in Table 6, the raw materials and blending ratios used were different for each comparative example. That is, in Comparative Example 11, only the halogenated phthalimide derivative was used among the flame retardants, and in Comparative Example 9, only the halogenated phthalimide derivative was used.
In this case, only brominated polystyrene was used.
【表6】[Table 6]
【0029】実施例及び比較例の考察
上記実施例16によれば、この実施例の難燃性樹脂組成
物より成る試験片は、それぞれ引張り試験、曲げ試験及
びアイゾット衝撃試験の結果が示すように良好な物性を
有している。また、この実施例に係る樹脂組成物より成
るプレートとフィルムは、難燃剤の分散判定において、
白点が殆ど見られず、難燃剤がプレート中又はフィルム
中に良好に分散していることがわかる。このようにプレ
ート中又はフィルム中に難燃剤が良好に分散しているた
め、この実施例に係る樹脂組成物より成る2種類の試験
片は、燃焼試験の結果が示すように、それぞれ難燃性を
有している。Discussion of Examples and Comparative Examples According to Example 16 above, the test piece made of the flame-retardant resin composition of this example had the following properties as shown in the results of the tensile test, bending test, and Izod impact test, respectively. It has good physical properties. In addition, the plate and film made of the resin composition according to this example were used to determine the dispersion of flame retardant.
Almost no white spots were observed, indicating that the flame retardant was well dispersed in the plate or film. Because the flame retardant was well dispersed in the plate or film, the two types of test pieces made of the resin composition according to this example showed flame retardant properties, as shown by the results of the combustion test. have.
【0030】これに対して、比較例11によれば、難燃
剤のうち、ハロゲン化フタル酸イミド誘導体のみを使用
し、臭素化ポリスチレンを添加していないため、この比
較例に係る樹脂組成物より成るプレートとフィルムは、
それぞれ白点が多数目立ち、難燃剤がプレート中又はフ
ィルム中に良好に分散していないことがわかる。比較例
12によれば、難燃剤のうち、臭素化ポリスチレンのみ
を使用し、ハロゲン化フタル酸イミド誘導体を添加して
いないため、この比較例に係る樹脂組成物より成るプレ
ートとフィルムは、それぞれ白点が目立ち、難燃剤がプ
レート中又はフィルム中に良好に分散していないことが
わかる。また、これらの比較例では、引張り伸び率と衝
撃特性に問題があることに加えて、難燃性の試験におい
て試験片が厚い場合には難燃性が良好であるが、薄くな
ると難燃性が不良になった。On the other hand, according to Comparative Example 11, only a halogenated phthalic acid imide derivative was used among the flame retardants, and brominated polystyrene was not added. The plate and film consist of
Many white spots were noticeable in each case, indicating that the flame retardant was not well dispersed in the plate or film. According to Comparative Example 12, among the flame retardants, only brominated polystyrene was used and no halogenated phthalimide derivative was added, so the plate and film made of the resin composition according to this comparative example were white. The dots are noticeable, indicating that the flame retardant is not well dispersed in the plate or film. In addition, in these comparative examples, in addition to problems with tensile elongation and impact properties, in flame retardancy tests, when the test piece is thick, it has good flame retardancy, but when it becomes thin, it has poor flame retardancy. has become defective.
【0031】[0031]
【発明の効果】本発明に係る難燃性樹脂組成物によれば
、難燃剤が良好に分散しているため、難燃性が優れてい
る。また、優れた物性を備えながら、難燃助剤も含めた
難燃剤の添加量を少なくすることができ、経済性にも優
れている。[Effects of the Invention] The flame retardant resin composition according to the present invention has excellent flame retardancy because the flame retardant is well dispersed. In addition, while having excellent physical properties, the amount of flame retardants including flame retardant aids added can be reduced, and it is also excellent in economic efficiency.
Claims (3)
特徴とする難燃性樹脂組成物。 A:ポリオレフィン系樹脂 70〜96wt
%B:下記a、bを含む難燃剤 20〜
3wt%【化1】 b:臭素化ポリスチレンC:アンチモン酸化物
10〜1wt% 但し、A+B+C=100wt%1. A flame-retardant resin composition containing the following components A, B, and C. A: Polyolefin resin 70-96wt
%B: Flame retardant containing the following a and b 20~
3wt% [Formula 1] b: Brominated polystyrene C: Antimony oxide
10~1wt% However, A+B+C=100wt%
a/b=30〜70/70〜30(重量比)としたこと
を特徴とする請求項1記載の難燃性樹脂組成物。[Claim 2] The content ratio of a and b of the flame retardant (B) is:
The flame-retardant resin composition according to claim 1, characterized in that a/b=30-70/70-30 (weight ratio).
)の含有割合で、B/C=2〜4/1(重量比)とした
ことを特徴とする請求項1又は2記載の難燃性樹脂組成
物。[Claim 3] Flame retardant (B) and antimony oxide (C
) The flame-retardant resin composition according to claim 1 or 2, characterized in that the content ratio of B/C is 2 to 4/1 (weight ratio).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13849991A JPH04337343A (en) | 1991-05-13 | 1991-05-13 | Flame-retardant resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13849991A JPH04337343A (en) | 1991-05-13 | 1991-05-13 | Flame-retardant resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04337343A true JPH04337343A (en) | 1992-11-25 |
Family
ID=15223551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13849991A Withdrawn JPH04337343A (en) | 1991-05-13 | 1991-05-13 | Flame-retardant resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04337343A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004003071A1 (en) * | 2002-06-27 | 2004-01-08 | Albemarle Corporation | Flame retardant compositions |
US7202296B2 (en) | 2003-12-19 | 2007-04-10 | Albemarle Corporation | Flame retardant compositions and their use |
-
1991
- 1991-05-13 JP JP13849991A patent/JPH04337343A/en not_active Withdrawn
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004003071A1 (en) * | 2002-06-27 | 2004-01-08 | Albemarle Corporation | Flame retardant compositions |
US7202296B2 (en) | 2003-12-19 | 2007-04-10 | Albemarle Corporation | Flame retardant compositions and their use |
US7405254B2 (en) | 2003-12-19 | 2008-07-29 | Albemarle Corporation | Flame retardant compositions and their use |
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