JPS6234060B2 - - Google Patents
Info
- Publication number
- JPS6234060B2 JPS6234060B2 JP54021039A JP2103979A JPS6234060B2 JP S6234060 B2 JPS6234060 B2 JP S6234060B2 JP 54021039 A JP54021039 A JP 54021039A JP 2103979 A JP2103979 A JP 2103979A JP S6234060 B2 JPS6234060 B2 JP S6234060B2
- Authority
- JP
- Japan
- Prior art keywords
- lead
- stabilizer
- chlorine
- stabilizers
- composite
- 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
Links
- 239000011347 resin Substances 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 23
- 239000003381 stabilizer Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 13
- 239000000843 powder Substances 0.000 claims description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 239000006084 composite stabilizer Substances 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000000314 lubricant Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 239000002245 particle Substances 0.000 description 8
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 7
- 239000008187 granular material Substances 0.000 description 6
- 238000005469 granulation Methods 0.000 description 6
- 230000003179 granulation Effects 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000015278 beef Nutrition 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- OCWMFVJKFWXKNZ-UHFFFAOYSA-L lead(2+);oxygen(2-);sulfate Chemical compound [O-2].[O-2].[O-2].[Pb+2].[Pb+2].[Pb+2].[Pb+2].[O-]S([O-])(=O)=O OCWMFVJKFWXKNZ-UHFFFAOYSA-L 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 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 2
- 239000002131 composite material Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- RGTIBVZDHOMOKC-UHFFFAOYSA-N stearolic acid Chemical compound CCCCCCCCC#CCCCCCCCC(O)=O RGTIBVZDHOMOKC-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 206010027439 Metal poisoning Diseases 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 229910000004 White lead Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle 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
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 150000002611 lead compounds Chemical class 0.000 description 1
- 208000008127 lead poisoning Diseases 0.000 description 1
- YJOMWQQKPKLUBO-UHFFFAOYSA-L lead(2+);phthalate Chemical compound [Pb+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O YJOMWQQKPKLUBO-UHFFFAOYSA-L 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 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
- 239000004200 microcrystalline wax Substances 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- QRCJOCOSPZMDJY-UHFFFAOYSA-N valnoctamide Chemical compound CCC(C)C(CC)C(N)=O QRCJOCOSPZMDJY-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Description
【発明の詳細な説明】
本発明は塩素含有樹脂の加工の際に使用する複
合安定剤の造粒化の改良方法にして、数種の安定
剤及び塩素含有樹脂粉体を特別の条件で凝集粒状
とする非飛散性及び分散性良好な塩素含有樹脂複
合安定剤の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention is an improved method for granulating composite stabilizers used in the processing of chlorine-containing resins, in which several stabilizers and chlorine-containing resin powders are agglomerated under special conditions. The present invention relates to a method for producing a chlorine-containing resin composite stabilizer that is made into granules and has good non-scattering properties and good dispersibility.
一般に塩素含有樹脂用安定剤には金属石鹸系、
液状複合系、無機鉛系、純有機系、ワンパツケー
ジ系等があり、助剤としてはエポキシ化合物、抗
酸化剤、紫外線吸収剤、滑剤等が知られている。
然してこれらは単独でなく数種の組合わせによる
複合体として使用されるのが通常であり、塩素含
有樹脂に必要な安定剤をあらかじめ用途に応じた
割合に均一に混合したものを複合安定剤或いはワ
ンパツケージ安定剤と称している。 Generally, stabilizers for chlorine-containing resins include metal soaps,
There are liquid composite systems, inorganic lead systems, pure organic systems, one-package systems, etc., and known auxiliary agents include epoxy compounds, antioxidants, ultraviolet absorbers, and lubricants.
However, these are usually used not alone but as a composite of several types, and the stabilizers necessary for chlorine-containing resins are mixed uniformly in advance in proportions depending on the application and are used as composite stabilizers or composite stabilizers. It is called a one-pack cage stabilizer.
無機鉛−金属石鹸を主体とする複合安定剤は粉
体であるために、取扱い梱包の際、粉塵が飛散す
る弊を有し、鉛化合物による鉛毒障害をまねく恐
れがある。従来これが対策として、安定剤の湿潤
化、ペースト化、粒状化の手段が採られている
が、湿潤化した安定剤、ペースト化し安定剤は自
由流動性がないため取扱いが不便で包装、計量等
の作業性能が悪く、且え等を使用する塩化ビニル
の軟質、硬質等の加工目的によつて使用上の範囲
が制限される。また粒状化した安定剤は粒状化の
方法(粒状化の工程)によつて複合安定剤の組成
や品質に何等かの制約をうける。特に無機鉛成分
の量比の大きい配合では飛散性の問題が残されて
いる。 Since the composite stabilizer mainly composed of inorganic lead and metal soap is in the form of powder, it has the disadvantage of scattering dust during handling and packaging, which may lead to lead poisoning problems due to lead compounds. Conventional countermeasures have been to moisten the stabilizer, make it into a paste, or make it into granules, but moistened stabilizers or stabilizers made into a paste do not have free-flowing properties and are therefore inconvenient to handle, making packaging, measuring, etc. Its working performance is poor, and its range of use is limited depending on the purpose of processing, such as whether the vinyl chloride used is soft or hard. Furthermore, the granulated stabilizer is subject to some restrictions on the composition and quality of the composite stabilizer depending on the granulation method (granulation process). Particularly in formulations with a large proportion of inorganic lead components, the problem of scattering remains.
本発明の複合安定剤の造粒を抜本的に研究し、
合理的簡略な製法により従来より優れた製品を得
ることに成功したものである。 Fundamentally researched the granulation of the composite stabilizer of the present invention,
We have succeeded in obtaining a product that is superior to conventional products using a rationally simple manufacturing method.
本発明は(a)有機酸金属塩または滑剤の1種以
上、(b)無機鉛安定剤及び必要によつてその他の安
定剤を急速粉体混合機を用いて均一に混合すると
共に、外部加熱または摩擦熱により粒状化するに
際し5〜30重量%の塩素含有樹脂粉末を添加する
ことを特徴とする塩素含有樹脂用複合安定剤の製
造方法であることを要旨とする。 The present invention involves uniformly mixing (a) one or more organic acid metal salts or lubricants, (b) an inorganic lead stabilizer, and other stabilizers as necessary using a rapid powder mixer, and external heating. Alternatively, the present invention provides a method for producing a composite stabilizer for a chlorine-containing resin, characterized in that 5 to 30% by weight of a chlorine-containing resin powder is added during granulation by frictional heat.
本発明で使用する有機酸金属塩としては、最も
一般的には牛脂脂肪酸、他に炭素数12〜29の飽和
脂肪酸、クロトン酸、エライジン酸、ブラシジン
酸、ステアロール酸等の不飽和脂肪酸、牛脂脂肪
酸以外の天然脂肪酸混合物等のPb、Ca、Ba、
Mg、Sr、Zn、Cd塩が挙げられ好ましくは融点が
200℃以下で常温下固体状を呈するものである。 The organic acid metal salt used in the present invention is most commonly beef tallow fatty acid, as well as saturated fatty acids having 12 to 29 carbon atoms, unsaturated fatty acids such as crotonic acid, elaidic acid, brassic acid, stearolic acid, beef tallow, etc. Natural fatty acid mixtures other than fatty acids such as Pb, Ca, Ba,
Mg, Sr, Zn, Cd salts may be mentioned, preferably those with a melting point
It exhibits a solid state at room temperature below 200℃.
滑剤としては高級脂肪酸またはそのエステル、
マイクロワツクス、ポリエチレンワツクス、ステ
アリン酸アミド、多価アルコールまたはそのエス
テル、硬化ヒマシ油、エチレングリコールモノス
テアレート、ステアリルアルコール等が挙げられ
る。 As a lubricant, higher fatty acids or their esters,
Examples include micro wax, polyethylene wax, stearic acid amide, polyhydric alcohol or its ester, hydrogenated castor oil, ethylene glycol monostearate, and stearyl alcohol.
また無機鉛安定剤としては、例えば鉛白、三塩
基性硫酸鉛、塩基性亜硫酸鉛、二塩基性亜リン酸
鉛、二塩基性フタル酸鉛、三塩基性マレイン酸
鉛、塩基性ケイ酸鉛等を挙げることができる。 Examples of inorganic lead stabilizers include white lead, tribasic lead sulfate, basic lead sulfite, dibasic lead phosphite, dibasic lead phthalate, tribasic lead maleate, and basic lead silicate. etc. can be mentioned.
次に塩素含有樹脂粉体としては市販の塩化ビニ
ル樹脂、塩化ビニル−酢酸ビニル共重合体、塩化
ビニリデン樹脂、塩素化ポリエチレン等が使用で
きるが、これら粉体樹脂の使用量は複合安定剤全
量に対し5〜30重量%の間が好適である。粉体樹
脂が5%以下であれば生成物の飛散性防止効果が
不満足となり、また製品の使用時における樹脂へ
の分散性も充分とはなり得ない。 Next, as the chlorine-containing resin powder, commercially available vinyl chloride resin, vinyl chloride-vinyl acetate copolymer, vinylidene chloride resin, chlorinated polyethylene, etc. can be used, but the amount of these powder resins used is the total amount of the composite stabilizer. It is preferably between 5 and 30% by weight. If the powder resin content is less than 5%, the effect of preventing the product from scattering will be unsatisfactory, and the dispersibility in the resin during use of the product will not be sufficient.
一方、30%以上使用しても、より以上の飛散性
改善効果はみられず、かえつて不経済である。 On the other hand, even if it is used in an amount of 30% or more, no further improvement in scattering properties is observed, which is rather uneconomical.
本発明ではその他必要に応じて、他の安定化助
剤例えばエポキシ化合物、抗酸化剤を使用しても
よいし、また紫外線吸収剤、充填剤を混合併用す
ることもできる。 In the present invention, other stabilizing aids such as epoxy compounds and antioxidants may be used as necessary, and ultraviolet absorbers and fillers may also be used in combination.
本発明より製した安定剤は適宜粗粒、微粒を篩
分けることにより所要な粒径として実用に供せら
れるが、粒度28〜150メツシユのものを、従来よ
りも高収率で得ることができることも本発明の特
徴である。 The stabilizer produced according to the present invention can be put to practical use in the desired particle size by appropriately sieving coarse particles and fine particles, but it is possible to obtain a stabilizer with a particle size of 28 to 150 mesh at a higher yield than conventional methods. This is also a feature of the present invention.
本発明の実施について、急速混合機として、例
えばヘンシエルミキサー、スーパーミキサー等を
用いる。急速混合機のロータの回転で組成混合物
に摩擦による熱を生ぜしめ混合物中の可融物質を
熔融温度直前まで温度上昇せしめるには、一定の
回転数と〓練時間の関係がある。 For carrying out the present invention, a rapid mixer such as a Henschel mixer, a super mixer, etc. is used. In order to generate frictional heat in the composition mixture by the rotation of the rotor of the rapid mixer and to raise the temperature of the molten substance in the mixture to just before the melting temperature, there is a relationship between a certain rotation speed and kneading time.
実験研究によると、ロータが撹拌混合する状態
においては組成混合物の温度は相互の摩擦により
生ずる熱で緩やかに上昇しつづけ、可融物質の表
面がその熔融点以前の温度近くになると、ロータ
の回転負荷が急速に増大して、電動機の電流負荷
が急増し、物質温度も急激な変動を見せる。この
点を電流計等で見定めて測定し制御することによ
つてシンターリング造粒を結果づけるのである。 According to experimental research, when the rotor is stirring and mixing, the temperature of the composition mixture continues to rise slowly due to the heat generated by mutual friction, and when the surface of the fusible substance reaches a temperature close to its melting point, the rotation of the rotor stops. The load increases rapidly, the current load on the motor increases rapidly, and the material temperature also exhibits rapid fluctuations. Sintering granulation is achieved by identifying, measuring, and controlling this point using an ammeter or the like.
また造粒作業を促進せしめるために外部から適
宜加熱を行うこともできる。 Further, in order to accelerate the granulation operation, heating can be applied from the outside as appropriate.
実施例 1
三塩基性硫酸鉛35Kg、ステアリン酸鉛5Kg、抗
酸化剤(ビスフエノールA)1Kgおよびポリ塩化
ビニル樹脂粉末(ゼオン103EP)9Kgを200の
スーパーミキサーによつて混合し内部温度90℃で
15分間混合造粒した。生成した造粒物を篩分けし
粒度28〜150メツシユの低飛散性のものを85%の
収率で得た。Example 1 35 kg of tribasic lead sulfate, 5 kg of lead stearate, 1 kg of antioxidant (bisphenol A) and 9 kg of polyvinyl chloride resin powder (Zeon 103EP) were mixed in a 200 super mixer and the mixture was heated at an internal temperature of 90°C.
Mix and granulate for 15 minutes. The produced granules were sieved to obtain particles with a particle size of 28 to 150 mesh and low scattering properties at a yield of 85%.
またこのものの塩化ビニル樹脂への分散性を試
験したところ優れた分散性を示した。即ち塩化ビ
ニル樹脂100重量部、フタル酸ジオクチル50部、
ウオツチングレツドトーナー1部、粒状安定剤5
部を軽く混合しプラストグラフで180℃、20分間
混練し半ゲル化状物質を6インチミキシングロー
ル(温度160℃)でシート状として取出し、シー
ト中に存在する粒子の状態を肉眼で判定した。 Further, when the dispersibility of this product in vinyl chloride resin was tested, it showed excellent dispersibility. That is, 100 parts by weight of vinyl chloride resin, 50 parts of dioctyl phthalate,
1 part of watching red toner, 5 parts of granular stabilizer
The semi-gelled material was taken out as a sheet using a 6-inch mixing roll (temperature: 160°C), and the state of the particles present in the sheet was visually determined.
尚、上記配合においてポリ塩化ビニル樹脂粉末
を除いた配合を同様の方法で造粒したものは収率
が40%程度であり、しかも飛散性、分散性共に不
満足な状態であつた。 In addition, when the above formulation except for the polyvinyl chloride resin powder was granulated using the same method, the yield was about 40%, and both the scatterability and dispersibility were unsatisfactory.
実施例 2
三塩基性硫酸鉛40Kg、牛脂脂肪酸2.7Kgおよび
ポリ塩化ビニル樹脂10.7Kgを200のスーパーミ
キサーによつて混合し、内部温度73℃で10分間混
合造粒した。生成した造粒物を篩分けし粒度28〜
150メツシユの低飛散性のものを90%の収率で得
た。またこのものの塩化ビニル樹脂への分散性を
実施例1と同様の方法で試験したところ、優れた
分散性を示した。Example 2 40 kg of tribasic lead sulfate, 2.7 kg of beef tallow fatty acid and 10.7 kg of polyvinyl chloride resin were mixed in a 200 super mixer and mixed and granulated for 10 minutes at an internal temperature of 73°C. The generated granules are sieved and the particle size is 28~
A low-scattering product of 150 mesh was obtained with a yield of 90%. Further, when the dispersibility of this product in vinyl chloride resin was tested in the same manner as in Example 1, it showed excellent dispersibility.
実施例 3
二塩基性亜硫酸鉛30Kg、ステアリン酸鉛15Kg、
ステアリン酸カルシウム5Kgおよび塩化ビニル樹
脂13Kgを200のスーパーミキサーによつて混合
し、内部温度105℃で30分間混合造粒した。Example 3 Dibasic lead sulfite 30Kg, lead stearate 15Kg,
5 kg of calcium stearate and 13 kg of vinyl chloride resin were mixed in a 200 super mixer and mixed and granulated for 30 minutes at an internal temperature of 105°C.
生成した造粒物を篩分けし粒度28−150メツシ
ユの低飛性のものを90%の収率で得た。またこの
ものの塩化ビニル樹脂への分散性を実施例1と同
様の方法で試験したところ、優れた分散性を示し
た。また、上記配合においてポリ塩化ビニル樹脂
粉末を除いた配合を同様の方法で造粒したものは
収率45%程度であり、しかも飛散性、分散性が不
満足なものであつた。 The produced granules were sieved to obtain particles with a particle size of 28-150 mesh and low flyability with a yield of 90%. Further, when the dispersibility of this product in vinyl chloride resin was tested in the same manner as in Example 1, it showed excellent dispersibility. Furthermore, when the above formulation except for the polyvinyl chloride resin powder was granulated using the same method, the yield was about 45%, and the scatterability and dispersibility were unsatisfactory.
Claims (1)
機鉛安定剤及び必要によつてその他の安定剤を急
速粉体混合機を用いて均一に混合すると共に、外
部加熱または摩擦熱により粒状化するに際し、5
〜30重量%の塩素含有樹脂粉末を添加することを
特徴とする塩素含有樹脂用複合安定剤の製造方
法。1. Mix uniformly (a) one or more organic acid metal salts or lubricants, (b) an inorganic lead stabilizer, and other stabilizers as necessary using a rapid powder mixer, and then apply external heat or friction. When granulating by heat, 5
A method for producing a composite stabilizer for chlorine-containing resins, which comprises adding ~30% by weight of chlorine-containing resin powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2103979A JPS55115437A (en) | 1979-02-23 | 1979-02-23 | Preparation of composite stabilizer for chlorine- containing resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2103979A JPS55115437A (en) | 1979-02-23 | 1979-02-23 | Preparation of composite stabilizer for chlorine- containing resin |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55115437A JPS55115437A (en) | 1980-09-05 |
JPS6234060B2 true JPS6234060B2 (en) | 1987-07-24 |
Family
ID=12043800
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2103979A Granted JPS55115437A (en) | 1979-02-23 | 1979-02-23 | Preparation of composite stabilizer for chlorine- containing resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55115437A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58141224A (en) * | 1982-02-17 | 1983-08-22 | Mitsui Petrochem Ind Ltd | Thermoplastic elastomer composition for calendering |
JPS5958047A (en) * | 1982-09-29 | 1984-04-03 | Mizusawa Ind Chem Ltd | Granular stabilizer for chlorine-containing polymer and its preparation |
GB8617186D0 (en) * | 1986-07-15 | 1986-08-20 | Ici Plc | Dispersed particulate composition |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5153546A (en) * | 1974-11-06 | 1976-05-12 | Nitto Kasei Co Ltd | HAROGENGANJUJUSHOKARYUJOANTEIZAISOSEIBUTSUNO SEIHO |
-
1979
- 1979-02-23 JP JP2103979A patent/JPS55115437A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5153546A (en) * | 1974-11-06 | 1976-05-12 | Nitto Kasei Co Ltd | HAROGENGANJUJUSHOKARYUJOANTEIZAISOSEIBUTSUNO SEIHO |
Also Published As
Publication number | Publication date |
---|---|
JPS55115437A (en) | 1980-09-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3461081A (en) | Stabilizing agent for a halogen containing synthetic resin consisting of a basic inorganic acid salt of lead coated with a fatty acid soap of lead,cadmium or calcium | |
JPS6363752A (en) | Polymer concentrate and its production | |
KR20130004142A (en) | Process to prepare additive packages for use in pvc compounding | |
JPS6234060B2 (en) | ||
JPS5958047A (en) | Granular stabilizer for chlorine-containing polymer and its preparation | |
US4501840A (en) | Alkaline modified pentaerythritol stabilizer for vinyl chloride resin | |
NO833488L (en) | STABILIZATION OF POLYMERS USING CITRATE SALTS | |
JPH0368638A (en) | Stabilized phosphite composition | |
US3668144A (en) | Dust-free lead stabilizer for synthetic resins | |
US3905927A (en) | Dustless free-flowing lead stabilizer compositions for polyvinyl chloride | |
US3849365A (en) | Method for production of plasticized thermoplastic powder mixtures | |
US2598319A (en) | Dustless composition for rubber compounding and method of making same | |
US4711921A (en) | Stabilization of vinyl chloride polymers | |
US3185599A (en) | Process of producing welding fluxes | |
JP3174598B2 (en) | Method for producing vinyl chloride resin composition | |
JPS6220538A (en) | Granules | |
JPH0768411B2 (en) | Method for producing powder-free metal-containing stabilizer particles and halogen-containing polymer stabilized with the particles | |
JP3602610B2 (en) | Molded peptizer that does not cause caking | |
US4591452A (en) | Solid multicomponent mixtures of stabilizers and lubricants for halogenated polymers and the preparation thereof | |
JP3618091B2 (en) | Composite stabilizer particles for chlorine-containing polymer and the resin composition | |
US4263200A (en) | Free flowing chloropolyethylene, its manufacture and use | |
US4025690A (en) | Method of preparing additives and additives prepared according to said method | |
DE2124040B2 (en) | Process for the production of a granulated stabilizer preparation for vinyl chloride polymers | |
GB1595044A (en) | Process for the low temperature conditioning of vinyl chloride polymer stabilisers | |
DE1667178A1 (en) | Process for the production of agglomerates from finely divided solid materials |