JPS606741A - Vinyl chloride resin composition - Google Patents
Vinyl chloride resin compositionInfo
- Publication number
- JPS606741A JPS606741A JP11294883A JP11294883A JPS606741A JP S606741 A JPS606741 A JP S606741A JP 11294883 A JP11294883 A JP 11294883A JP 11294883 A JP11294883 A JP 11294883A JP S606741 A JPS606741 A JP S606741A
- Authority
- JP
- Japan
- Prior art keywords
- vinyl chloride
- copolymer
- chloride resin
- dicyclopentadiene
- maleic anhydride
- 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.)
- Granted
Links
Abstract
Description
【発明の詳細な説明】
記する)の体積抵抗率(以下VRと略記する)を向上さ
せた組成物に関する。DETAILED DESCRIPTION OF THE INVENTION This invention relates to a composition with improved volume resistivity (hereinafter abbreviated as VR).
元7来、pvcは体積抵抗率の大きいプラスチックであ
シ、電気絶縁材料として使用されているが、PVCの製
造工程や加工工程で微量の金属イオンや比較的イオン化
傾向の高い金属化合物が混入し、これによ5vRの低下
が起る。これら金属イオン等の混入を完全に防止する事
は現実に極めて困難である。PVC has been a plastic with a high volume resistivity and has been used as an electrical insulating material since the beginning of the 7th century, but trace amounts of metal ions and metal compounds with a relatively high tendency to ionize are mixed in during the manufacturing and processing processes of PVC. , which causes a decrease in 5vR. In reality, it is extremely difficult to completely prevent the contamination of these metal ions.
本発明者らは、上記金属イオン等を捕捉し、その影響力
を無くすことにより、pvcのVRを向上させる方法を
鋭意検討した結果、ジシクロペンクジエンと無水マレイ
ン酸の共重合体(以下D−Mコポリマーと略称する)を
特定量添加する事により得られたPvC組成物のVRが
向上する事を見い出し本発明に到った。The present inventors have intensively investigated a method for improving the VR of PVC by capturing the metal ions and eliminating their influence. It was discovered that the VR of the obtained PvC composition was improved by adding a specific amount of -M copolymer), and the present invention was achieved.
本発明は、D−Mコポリマーをpva当シα005〜5
重量%添加する事を特徴とするVRの大きいpvcの組
成物である。The present invention uses a D-M copolymer with pva α005~5
This is a PVC composition with a large VR, characterized by adding % by weight.
本発明で言うpvaとは、塩化ビニルホモポリマーの外
に塩化ビニルと共重合゛可能な単量体、例えばエチレン
,プロピレン,酢゛酸ビニル,プロビオン酸ビニル,ア
クリル酸,アクリル酸エステル。In the present invention, pva refers to not only vinyl chloride homopolymers but also monomers copolymerizable with vinyl chloride, such as ethylene, propylene, vinyl acetate, vinyl propionate, acrylic acid, and acrylic esters.
ビニルエーテル類,その他種々の公知の共重合可能な単
量体と塩化ビニルの共重合体および塩化ビニルを主成分
とするグラフト共重合体を含み、懸濁重合,乳化重合,
塊状重合,気相重合等公知の重合法のいづれの方法によ
って得られたものでも使用し得る。Contains vinyl ethers, copolymers of vinyl chloride with various other known copolymerizable monomers, and graft copolymers mainly composed of vinyl chloride, which can be used for suspension polymerization, emulsion polymerization,
Those obtained by any known polymerization method such as bulk polymerization or gas phase polymerization may be used.
本発明で使用するD−Mコポリマーの分子量は、特に範
囲を限定するものではないが、実用上1000〜200
00程度のものが好ましい。D−Mコポリマーのジシク
ロペンタジエント無水マレイン酸の共重合比はジシクロ
ペンタジェン1モルに対し、無水マレイン酸1〜2モル
であり、酸価は100以上である事が好”ましい。Although the molecular weight of the D-M copolymer used in the present invention is not particularly limited, it is practically 1000 to 200.
A value of about 00 is preferable. The copolymerization ratio of dicyclopentadiene maleic anhydride in the DM copolymer is 1 to 2 mol of maleic anhydride per 1 mol of dicyclopentadiene, and the acid value is preferably 100 or more.
D−Mコポリマーはジシクロペンタジェン、無水マレイ
ン酸、溶剤、触媒を反応器に入れて撹拌しながら加熱し
、反応終了後溶剤及び未反応物を分離して得ることがで
きる。The DM copolymer can be obtained by placing dicyclopentadiene, maleic anhydride, a solvent, and a catalyst in a reactor, heating it while stirring, and separating the solvent and unreacted materials after the reaction is completed.
D−Mコポリマーの添加量は多い程VR向上効果が大き
くなるが、’pvcに対し5重量係を超えると他の物性
への影響が大きくなる為実用的でない。また、a005
重量−以下ではほとんどVR改良効果が認められない。The larger the amount of the D-M copolymer added, the greater the VR improvement effect, but if it exceeds a weight ratio of 5 to 'pvc, it is not practical because the influence on other physical properties becomes large. Also, a005
If the weight is less than -, almost no VR improvement effect is observed.
D−MコポリマーをPVOに添加する時期は、pvcの
重合前9重合中9重合終了時あるいは成形加工時いずれ
でも良いが、成形加工時よりも重合時に添加する方が同
一添加量ではVR向上効果が大きい傾向がみられる。D-M copolymer may be added to PVO at the end of 9 polymerizations before PVC polymerization or at the time of molding, but adding it during polymerization is more effective in improving VR at the same amount than during molding. There is a tendency for there to be a large
P V OiCT) −Mコポリマーを添加し、成形加
工するに当っては常法に従って可塑剤、滑剤、安定剤2
着色剤等を配合して均一混合し、押出成形機。P V OiCT)-M copolymer is added and plasticizers, lubricants, and stabilizers 2 are added in accordance with conventional methods during molding.
Add colorants, etc., mix uniformly, and extrude.
カレンダーロール、射出成形機等により成形する。Molded using calender rolls, injection molding machines, etc.
次に実例をあけて本発明の組成物を更に具体的に説明す
る。Next, the composition of the present invention will be explained in more detail with reference to examples.
実施例1
a 6−反応器に純水30001t9.塩化ビニルモノ
マー2000kg、夕シャリブチルパーオキシネオデカ
ネートn、6に9.水溶性ポリビニルアルコール1.6
IC9を入れ、攪拌しながら57℃に加熱した。重合
は圧力がt Okg /cl低下するまで行い、約80
チの転化率を得た。Example 1 a 6-30001t of pure water in the reactor9. 2000 kg of vinyl chloride monomer, butyl peroxyneodecanate n, 6 and 9. Water-soluble polyvinyl alcohol 1.6
IC9 was added and heated to 57° C. with stirring. Polymerization was carried out until the pressure decreased by tOkg/cl, approximately 80
The conversion rate of H was obtained.
得られた生成物100部、DOP50部、三塩基性硫酸
鉛5部を混合し7.150℃に加熱したロールで10分
間混練した後、170℃で5分間プレスして約1. Q
v+m厚のシートを作成した。100 parts of the obtained product, 50 parts of DOP, and 5 parts of tribasic lead sulfate were mixed and kneaded for 10 minutes using rolls heated to 7.150°C, and then pressed for 5 minutes at 170°C to give a mixture of about 1. Q
A sheet having a thickness of v+m was created.
このシートのVRをJ I S−に、−6723に準じ
た方法で測定し比較のデータとしだ。The VR of this sheet was measured in accordance with JIS-6723 and used as data for comparison.
b 分子量5oco、酸価250(7)D Mコポリマ
ーを、重合開始前に塩化ビニルモノマー当りQ、005
重量%添加する点を除いてaと同様に行った。b Molecular weight 5 oco, acid value 250 (7) DM copolymer was added with Q, 005 per vinyl chloride monomer before the start of polymerization.
The same procedure as a was carried out except that the weight percent was added.
cbに記したD−Mコポリマーを重合開始前に塩化ビニ
ルモノマー当り0.05重t%添加する点を除いてaと
同様に行った。The same procedure as a was carried out except that 0.05 wt % of the D-M copolymer described in cb was added per vinyl chloride monomer before the start of polymerization.
dbに記したD−Mコポリマーを重合終了時に塩化ビニ
ルモノマー当り0.05重量%添加する点を除いてaと
同様に行った。The same procedure as a was carried out except that 0.05% by weight of the DM copolymer described in db was added at the end of the polymerization based on the vinyl chloride monomer.
D−Mコポリマーは下記処方によりジシクロペンタジェ
ン、無水マレイン酸、溶剤、触媒を反応器に入れて攪拌
しながら加熱し、反応終了後溶剤及び未反応物を分離し
て得た。The DM copolymer was obtained by placing dicyclopentadiene, maleic anhydride, a solvent, and a catalyst in a reactor and heating while stirring, and after the reaction was completed, the solvent and unreacted materials were separated.
実施例1のVR測定結果を表−1に示す。The VR measurement results of Example 1 are shown in Table-1.
表−1
実施例2
a 懸濁重合法により得た重合度1000のボモPVC
100部、DOP5[]部、三塩基性硫酸鉛5部を混合
し、150℃に加熱したロールで10分間混練した後、
170℃で5分間プレスして約1.0鰭厚のシートを作
成した。このシートのVRを、JIS−に−,6723
に準じた方法で測定し比較のデータとした。Table-1 Example 2 a Bomo PVC with a degree of polymerization of 1000 obtained by suspension polymerization method
After mixing 100 parts of DOP, 5 parts of DOP, and 5 parts of tribasic lead sulfate and kneading for 10 minutes with a roll heated to 150°C,
A sheet having a thickness of about 1.0 fin was prepared by pressing at 170° C. for 5 minutes. VR of this sheet to JIS-, 6723
The data was measured using a method similar to that of the above and used as data for comparison.
b 分子量20000 、酸価250のD−Mコポリマ
ーを表−2に記した割合で添加する点を除いてaと同様
に行った。b The same procedure as a was carried out except that a DM copolymer having a molecular weight of 20,000 and an acid value of 250 was added in the proportions shown in Table 2.
D−Mコポリマーは下記処分により得た。The DM copolymer was obtained by the following procedure.
実施例2のVR測定結果を表−2に示す。The VR measurement results of Example 2 are shown in Table-2.
表−?Table-?
Claims (1)
ジシクロペンクジエンと無水マレイン酸の共重合体00
05〜5重量%とから成る塩化ビニル系樹脂組成物。(1) Copolymer of vinyl chloride resin 99.995-95%], dicyclopencdiene, and maleic anhydride 00
A vinyl chloride resin composition comprising 0.05 to 5% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11294883A JPS606741A (en) | 1983-06-24 | 1983-06-24 | Vinyl chloride resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11294883A JPS606741A (en) | 1983-06-24 | 1983-06-24 | Vinyl chloride resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS606741A true JPS606741A (en) | 1985-01-14 |
JPH035422B2 JPH035422B2 (en) | 1991-01-25 |
Family
ID=14599523
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11294883A Granted JPS606741A (en) | 1983-06-24 | 1983-06-24 | Vinyl chloride resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS606741A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62149742A (en) * | 1985-12-25 | 1987-07-03 | Toyo Soda Mfg Co Ltd | Vinyl chloride polymer composition |
-
1983
- 1983-06-24 JP JP11294883A patent/JPS606741A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62149742A (en) * | 1985-12-25 | 1987-07-03 | Toyo Soda Mfg Co Ltd | Vinyl chloride polymer composition |
Also Published As
Publication number | Publication date |
---|---|
JPH035422B2 (en) | 1991-01-25 |
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