JP2001059059A - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JP2001059059A JP2001059059A JP11274944A JP27494499A JP2001059059A JP 2001059059 A JP2001059059 A JP 2001059059A JP 11274944 A JP11274944 A JP 11274944A JP 27494499 A JP27494499 A JP 27494499A JP 2001059059 A JP2001059059 A JP 2001059059A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- resin
- resin composition
- plural kinds
- 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
- 239000011342 resin composition Substances 0.000 title claims abstract description 12
- 229920005989 resin Polymers 0.000 claims abstract description 35
- 239000011347 resin Substances 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 22
- -1 ester compound Chemical class 0.000 claims abstract description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 239000002253 acid Substances 0.000 claims abstract description 3
- 125000002723 alicyclic group Chemical group 0.000 claims abstract description 3
- 125000003118 aryl group Chemical group 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 239000011256 inorganic filler Substances 0.000 claims description 2
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 2
- 239000012766 organic filler Substances 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
- 238000004898 kneading Methods 0.000 abstract description 5
- 230000006866 deterioration Effects 0.000 abstract description 3
- 238000002845 discoloration Methods 0.000 abstract description 3
- 229920003023 plastic Polymers 0.000 abstract description 3
- 239000004033 plastic Substances 0.000 abstract description 3
- 238000013329 compounding Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 8
- 239000003381 stabilizer Substances 0.000 description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000002699 waste material Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- CMCJNODIWQEOAI-UHFFFAOYSA-N bis(2-butoxyethyl)phthalate Chemical compound CCCCOCCOC(=O)C1=CC=CC=C1C(=O)OCCOCCCC CMCJNODIWQEOAI-UHFFFAOYSA-N 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 2
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920006266 Vinyl film Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は複数種の樹脂混合物
を混練して均一分散する樹脂組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition in which plural kinds of resin mixtures are kneaded and uniformly dispersed.
【0002】[0002]
【従来の技術】類似の樹脂、例えば非極性樹脂同士、ま
たは極性樹脂同士では割合容易に溶融混合するが、非極
性樹脂と極性樹脂、例えばポリオレフィン系樹脂と塩化
ビニル系樹脂は通常の加工混練機では均一に分散するこ
とは出来ない。そして、これらの混合物を最終製品に成
形した時、外観上でも、品質的にも殆どの場合使用に耐
えないのが現状である。然るに、最近盛んに合成樹脂の
マテリアルリサイクルの必要性が叫ばれているが、回収
される樹脂が均一組成であることは希であり、複数種の
混合物であるのが普通である。この混合物を有効に資源
化するためには、同一組成物に分別することも1つの手
段かも知れぬが経済性から考えると、均一に分散、混合
混錬する方が効率的である。2. Description of the Related Art Similar resins, such as non-polar resins or polar resins, are easily melted and mixed, but non-polar resins and polar resins, such as polyolefin resins and vinyl chloride resins, are mixed with a conventional processing kneader. Cannot be dispersed uniformly. At the present time, when these mixtures are molded into final products, they are almost unusable in appearance and quality in most cases. However, although the necessity of material recycling of synthetic resins has been actively talked about recently, recovered resins are rarely of a uniform composition, and are usually a mixture of plural kinds. In order to effectively use this mixture as a resource, it may be one means to separate the mixture into the same composition. However, from the viewpoint of economy, it is more efficient to uniformly disperse and mix and knead the mixture.
【0003】均一に混練混合する方法としては、一つは
非極性樹脂と極性樹脂の共重合物を混合する方法があ
る。しかしこの方法は元々極性モノマーと非極性モノマ
ーの共重合が困難な場合が多く、例え共重合物が得られ
ても収率やモノマーコストの面から経済性に問題が多く
実用化されている例は少ない。As a method of uniformly kneading and mixing, there is a method of mixing a copolymer of a nonpolar resin and a polar resin. However, in this method, it is often difficult to copolymerize a polar monomer and a non-polar monomer from the beginning, and even if a copolymer is obtained, there are many economical problems in terms of yield and monomer cost, and this method has been put to practical use. Is less.
【0004】もう一つの方法は特殊な加工混練機を用い
強制的にシェアーを加えて混錬分散させる方法である。
しかしこの方法ではシェアーにより樹脂の劣化が起こり
やすく、樹脂の変色、臭い、又は加工中の発煙等により
実用化が困難な場合が多い。Another method is a method of forcibly adding a shear by using a special processing kneader to knead and disperse.
However, in this method, the resin tends to deteriorate due to shearing, and it is often difficult to put the resin into practical use due to discoloration, odor, smoke during processing, or the like.
【0005】[0005]
【本発明が解決しようとする課題】汎用の加工混練機及
び通常の加工条件で、変色、劣化なく、均一に混合混練
できる複数種の樹脂混合物をベースとした樹脂組成物を
提供すること。SUMMARY OF THE INVENTION An object of the present invention is to provide a general-purpose processing kneader and a resin composition based on a plurality of resin mixtures which can be uniformly mixed and kneaded without discoloration or deterioration under ordinary processing conditions.
【0006】[0006]
【課題を解決するための手段】本発明者は上記課題につ
いて検討の結果、複数種の樹脂混合物100重量部に対
し、一般化学式が次式で示される少なくとも1つのエー
テル結合を有するエステル系化合物The inventors of the present invention have studied the above problems, and as a result, based on 100 parts by weight of a mixture of plural kinds of resins, an ester compound having at least one ether bond represented by the following general formula.
【化1】Embedded image
【0007】 R(EO)mOOC−X−COO(EO)nR (式1) (式中、Xは炭素数2〜12のアルキル基、芳香族基、
若しくは脂環式の二塩基酸残基を、Rは同一又は異なっ
てもよい炭素数1〜15のアルキル基を、Eは炭素数2
〜4のアルキレン基をそれぞれ表わし、mは1〜7の整
数であり、nは0〜7の整数である)1.0〜50.0
重量部を配合してなる樹脂組成物が本課題の解決策にな
ることを見出し本発明に至った。[0007] R (EO) m OOC-X -COO (EO) n R ( Formula 1) (wherein, X is an alkyl group having 2 to 12 carbon atoms, an aromatic group,
Or an alicyclic dibasic acid residue, R represents an alkyl group having 1 to 15 carbon atoms which may be the same or different, and E represents 2 carbon atoms.
And m represents an integer of 1 to 7 and n represents an integer of 0 to 7)
The present inventors have found that a resin composition containing parts by weight is a solution to the present problem, and have reached the present invention.
【0008】更に具合的に説明すると (1)複数種の樹脂混合物100重量部に対し、式1で
示されるエステル系化合物1.0〜50.0を配合して
なる樹脂組成物。1.0重量部以下では効果なく、5
0.0重量部以上になると加工混練機に食い込まず加工
が困難である。 (2)エステル系化合物に対し、更に0.1〜5.0重
量%の過塩素酸塩を添てなる請求項1記載の樹脂化合
物。0.1重量%以下では効果がなく、5.0重量%以
上ではむしろ樹脂の劣化を促進するので好ましくない。 (3)複数種の樹脂混合物100重量部に対し、更に1
80重量部未満の無機充填剤又は及び有機充填剤を配合
してなる請求項1若しくは2項記載の樹脂組成物。18
0重量部以上になると通常の加工機では混合混練が困難
である。More specifically, (1) a resin composition comprising 100 to 100 parts by weight of a mixture of plural kinds of resins and 1.0 to 50.0 of an ester compound represented by the formula 1; No effect at less than 1.0 parts by weight, 5
If the amount is more than 0.0 parts by weight, it is difficult to work because it does not bite into the working kneader. (2) The resin compound according to claim 1, further comprising 0.1 to 5.0% by weight of a perchlorate based on the ester compound. When the content is less than 0.1% by weight, there is no effect, and when the content is more than 5.0% by weight, the deterioration of the resin is rather accelerated. (3) One additional 100 parts by weight of the resin mixture of plural kinds
The resin composition according to claim 1 or 2, wherein the resin composition comprises less than 80 parts by weight of an inorganic filler or an organic filler. 18
If it is 0 parts by weight or more, it is difficult to mix and knead with a normal processing machine.
【0009】[0009]
【発明の実施の形態】本発明に用いられる樹脂に関して
は特に制限はないが複数種の樹脂において、極性樹脂と
非極性樹脂との混合物が特に効果的である。例えば、極
性樹脂としては、塩化ビニル樹脂、アクリル樹脂、酢酸
ビニル樹脂アマイド樹脂、尿素樹脂、フェノール樹脂、
ポリエステル樹脂、ポリウレタン樹脂、天然ゴム、各種
合成ゴム(エチレンプロピレンゴムを除く)等が挙げら
れる。BEST MODE FOR CARRYING OUT THE INVENTION The resin used in the present invention is not particularly limited, but among a plurality of kinds of resins, a mixture of a polar resin and a non-polar resin is particularly effective. For example, as the polar resin, vinyl chloride resin, acrylic resin, vinyl acetate resin amide resin, urea resin, phenol resin,
Examples include polyester resin, polyurethane resin, natural rubber, various synthetic rubbers (excluding ethylene propylene rubber), and the like.
【0010】非極性樹脂としては、低密度ポリエチレ
ン、高密度ポリエチレン、直鎖状低密度ポリエチレン、
メタロセン系ポリエチレン、ポリプロピレン及びその共
重合物、ポリブテン、ポリメチルペンテン−1、エチレ
ンプロピレンゴム等が挙げられる。As the non-polar resin, low density polyethylene, high density polyethylene, linear low density polyethylene,
Examples include metallocene-based polyethylene, polypropylene and copolymers thereof, polybutene, polymethylpentene-1, ethylene propylene rubber and the like.
【0011】本発明の組成物にあっては、通常合成樹脂
に添加される各種の添加剤、例えば、熱安定剤、抗酸化
剤、光安定剤、帯電防止剤、造核剤、滑剤、顔料、加工
助剤、衝撃改良剤等を本発明の目的を損なわない範囲で
併用することが出来る。In the composition of the present invention, various additives usually added to the synthetic resin, for example, heat stabilizers, antioxidants, light stabilizers, antistatic agents, nucleating agents, lubricants, pigments , A processing aid, an impact modifier and the like can be used in combination within a range not to impair the object of the present invention.
【0012】[0012]
【実施例1〜3、比較例1,2】塩化ビニル樹脂(S1
008重合度800;カネカ社製)50重量部、低密度
ポリエチレン(サンテックM2115、MI;1.3
5,旭化成製)50重量部、ワンパック安定剤(ポリエ
チレン樹脂50重量%、金属石鹸20重量%、ポリエチ
レンワックス20重量%、酸化防止剤5重量%、熱安定
剤5重量%よりなる)1.0重量部、錫系安定剤(KS
18;共同薬品社製)0.6重量部、エポキシ化大豆油
1.0重量部、カルシウムステアレート1.2重量部、
塩化ビニル用顔料マスターバッチ(フタロシアニンブル
ー20重量%含有;東洋インキ社製)2.5重量部に対
し、ジブチルセロソルブフタレート0,3.0,10,
30,60重量部配合し、80℃にセットした20Lミ
キサー(川田製作所製)にてドライアップするまで攪拌
した。この混合物を40mm単軸押出機(PSM40;
アイ・ケイジー社製)にて造粒した。(造粒条件;ダイ
ス温度185℃、スクリュー回転数25rpm) この造粒ペレットを190℃にセットしたプレス機で
0.4mm厚みのシートに成形し顔料の分散性から両樹
脂の混練分散性を評価した。又引張りテストを行い(オ
ートグラフS100型;島津製作所製)、引張強度、伸
びを測定した(JIS K6760)。その過程で試料
ダンベルの相剥離を観察した。その結果を表1に示す。Examples 1 to 3, Comparative Examples 1 and 2 Vinyl chloride resin (S1
008, polymerization degree 800; 50 parts by weight, manufactured by Kaneka Corporation, low-density polyethylene (Suntech M2115, MI; 1.3)
5, 50 parts by weight of Asahi Kasei), one pack stabilizer (consisting of 50% by weight of polyethylene resin, 20% by weight of metal soap, 20% by weight of polyethylene wax, 5% by weight of antioxidant, 5% by weight of heat stabilizer) 0 parts by weight, tin-based stabilizer (KS
18; manufactured by Kyodo Yakuhin) 0.6 parts by weight, epoxidized soybean oil 1.0 part by weight, calcium stearate 1.2 parts by weight,
2.5 parts by weight of a pigment masterbatch for vinyl chloride (containing 20% by weight of phthalocyanine blue; manufactured by Toyo Ink Co., Ltd.) was added to dibutyl cellosolve phthalate 0, 3.0, 10,
30 and 60 parts by weight were blended, and the mixture was stirred by a 20 L mixer (manufactured by Kawada Seisakusho) set at 80 ° C. until dried up. This mixture was mixed with a 40 mm single screw extruder (PSM40;
Granulated by IKG Co., Ltd.). (Granulation conditions: Die temperature: 185 ° C., screw rotation speed: 25 rpm) The granulated pellets were formed into a sheet having a thickness of 0.4 mm by a press set at 190 ° C., and the kneading dispersibility of both resins was evaluated from the dispersibility of the pigment. did. Further, a tensile test was performed (Autograph Model S100; manufactured by Shimadzu Corporation), and tensile strength and elongation were measured (JIS K6760). During the process, phase separation of the sample dumbbell was observed. Table 1 shows the results.
【0013】[0013]
【実施例4〜7、比較例3,4】塩化ビニル樹脂(S1
008重合度800;カネカ社製)50重量部、プロピ
レンの共重合物(トクヤマPER;トクヤマ社製)50
重量部、ワンパック安定剤1.0重量部、錫安定剤(K
S18;共同薬品社製)0.6重量部、エポキシ化大豆
油1.0重量部、カルシウムステアレート1.2重量
部、ジブチルセロソルブフタレート20重量部に対し、
過塩素酸リチウムを各々0,0.05、0.1、0.
3、1.0、2.0重量部を配合した。これを170℃
にセットした8インチ2本ロール(西村製作所製)に投
入、そのロールに対する巻付き状態、ロール間のバンク
の回転状態、5分間混練後ロールから取出す時の剥離状
態を観察した。更に取出したシートの表面状態の観察及
び80℃24時間熱処理後、シート表面の液体の滲み出
し状態を調べた。その結果を表2に示す。Examples 4 to 7, Comparative Examples 3 and 4 Vinyl chloride resin (S1
008, degree of polymerization 800; 50 parts by weight, manufactured by Kaneka Co., Ltd., 50 propylene copolymer (Tokuyama PER; manufactured by Tokuyama) 50
Parts by weight, 1.0 part by weight of one-pack stabilizer, tin stabilizer (K
S18; manufactured by Kyodo Yakuhin) 0.6 parts by weight, epoxidized soybean oil 1.0 part by weight, calcium stearate 1.2 parts by weight, dibutyl cellosolve phthalate 20 parts by weight,
Lithium perchlorate was added at 0, 0.05, 0.1, 0.
3, 1.0 and 2.0 parts by weight were blended. 170 ℃
Into a roll of 8 inches (manufactured by Nishimura Seisakusho), and the state of winding around the roll, the rotation of the bank between the rolls, the kneading state for 5 minutes, and the peeling state when removing from the roll were observed. Furthermore, after observing the surface state of the sheet taken out and heat-treating it at 80 ° C. for 24 hours, the state of seepage of liquid on the sheet surface was examined. Table 2 shows the results.
【0014】[0014]
【実施例8〜10、比較例5,6】使用済農業用ビニル
フィルム(以降廃農ビと略)の粉砕品(以降フラフと云
う)50重量部、使用済農業用ポリエチレンフィルム
(以降廃農ポリと略)のフラフ50重量部、ワンパック
安定剤1.0重量部に対し、ジエチルセロソルブアジペ
ートを各々0,3.0,10,30,60重量部配合
し、20Lミキサーで混合後、160〜180℃にセッ
トした8インチ2本ロールに投入し実施例4〜7と同様
の評価を行った。その結果を表3に示す。Examples 8 to 10 and Comparative Examples 5 and 6 50 parts by weight of a pulverized product (hereinafter referred to as fluff) of a used vinyl film for agriculture (hereinafter abbreviated as waste agricultural plastic) and a polyethylene film for a used agriculture (hereinafter abbreviated as waste agricultural With respect to 50 parts by weight of fluff (abbreviated as poly) and 1.0 part by weight of one-pack stabilizer, 0, 3.0, 10, 30, and 60 parts by weight of diethyl cellosolve adipate were blended, and mixed with a 20 L mixer. The same evaluation as in Examples 4 to 7 was carried out by feeding into two 8-inch rolls set at ~ 180 ° C. Table 3 shows the results.
【0015】[0015]
【実施例11〜13、比較例7】廃農ビのフラフ50重
量部、廃農ポリのフラフ50重量部、ワンパック安定剤
1.0重量部、過塩素酸リチウム1.5重量%を含むジ
エチルセロソルブアジペート30重量部に対し、タルク
(HK9;林化成製)を各々50,100,150、2
00、重量部を配合し、20Lミキサーにて混合後、1
75℃にセットした8インチ2本ロールに投入、実施例
4〜7と同様の評価を行った。その結果を表4に示すExamples 11 to 13 and Comparative Example 7 Including 50 parts by weight of waste agricultural plastic fluff, 50 parts by weight of waste agricultural poly fluff, 1.0 part by weight of one-pack stabilizer, and 1.5% by weight of lithium perchlorate. To 30 parts by weight of diethyl cellosolve adipate, talc (HK9; manufactured by Hayashi Kasei) was added to each of 50, 100, 150 and 2 parts.
, 100 parts by weight, and mixed with a 20 L mixer.
It was put into an 8-inch two-roll set at 75 ° C. and evaluated in the same manner as in Examples 4 to 7. Table 4 shows the results.
【0016】[0016]
【表1】 [Table 1]
【0017】[0017]
【表2】 [Table 2]
【0018】[0018]
【表3】 [Table 3]
【0019】[0019]
【表4】 [Table 4]
Claims (3)
一般化学式が次式で示される少なくとも1つのエーテル
結合を持つエステル系化合物 R(EO)mOOC−X−COO(EO)nR (式1) (式中、Xは炭素数2〜12のアルキル基、芳香族基、
若しくは脂環式の二塩基酸残基を、Rは同一又は異なっ
てもよい炭素数1〜15のアルキル基を、Eは炭素数2
〜4のアルキレン基をそれぞれ表わし、mは1〜7の整
数であり、nは0〜7の整数である)1.0〜50.0
重量部を配合してなる樹脂組成物。(1) 100 parts by weight of a mixture of plural kinds of resins,
At least an ester compound having one ether bond R (EO) m OOC-X -COO (EO) n R ( Formula 1) (wherein the general formula is represented by the following formula, X is an alkyl having 2 to 12 carbon atoms Group, aromatic group,
Or an alicyclic dibasic acid residue, R represents an alkyl group having 1 to 15 carbon atoms which may be the same or different, and E represents 2 carbon atoms.
And m represents an integer of 1 to 7 and n represents an integer of 0 to 7)
A resin composition containing parts by weight.
酸塩0.1〜5.0重量%を配合してなる請求項1記載
の樹脂組成物。2. The resin composition according to claim 1, further comprising 0.1 to 5.0% by weight of a perchlorate based on the ester compound.
て、更に180重量部未満の無機充填剤又は及び有機充
填剤を配合してなる請求項1若しくは請求項2記載の樹
脂組成物。3. The resin composition according to claim 1, further comprising less than 180 parts by weight of an inorganic filler and / or an organic filler based on 100 parts by weight of a mixture of plural kinds of resins.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11274944A JP2001059059A (en) | 1999-08-23 | 1999-08-23 | Resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11274944A JP2001059059A (en) | 1999-08-23 | 1999-08-23 | Resin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2001059059A true JP2001059059A (en) | 2001-03-06 |
Family
ID=17548740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11274944A Pending JP2001059059A (en) | 1999-08-23 | 1999-08-23 | Resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2001059059A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001079354A1 (en) * | 2000-04-12 | 2001-10-25 | Sanko Chemical Industry Co., Ltd. | Antistatic composition |
| JP2002020617A (en) * | 2000-07-06 | 2002-01-23 | Riken Technos Corp | Antistatic polyurethane resin composition |
| JP2002309097A (en) * | 2000-07-06 | 2002-10-23 | Riken Technos Corp | Antistatic resin composition |
| JP2003306590A (en) * | 2002-04-17 | 2003-10-31 | Riken Technos Corp | Thermoplastic resin composition |
| JP2011074400A (en) * | 2011-01-18 | 2011-04-14 | Riken Technos Corp | Antistatic polyurethane resin composition |
| JP2011084749A (en) * | 2011-01-18 | 2011-04-28 | Riken Technos Corp | Antistatic polyurethane resin composition |
-
1999
- 1999-08-23 JP JP11274944A patent/JP2001059059A/en active Pending
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001079354A1 (en) * | 2000-04-12 | 2001-10-25 | Sanko Chemical Industry Co., Ltd. | Antistatic composition |
| JP2002020617A (en) * | 2000-07-06 | 2002-01-23 | Riken Technos Corp | Antistatic polyurethane resin composition |
| JP2002309097A (en) * | 2000-07-06 | 2002-10-23 | Riken Technos Corp | Antistatic resin composition |
| JP2003306590A (en) * | 2002-04-17 | 2003-10-31 | Riken Technos Corp | Thermoplastic resin composition |
| JP2011074400A (en) * | 2011-01-18 | 2011-04-14 | Riken Technos Corp | Antistatic polyurethane resin composition |
| JP2011084749A (en) * | 2011-01-18 | 2011-04-28 | Riken Technos Corp | Antistatic polyurethane resin composition |
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