JPS59145232A - Sulfohalogenated polyolefin latex composition and vulcanization of film prepared therefrom - Google Patents

Sulfohalogenated polyolefin latex composition and vulcanization of film prepared therefrom

Info

Publication number
JPS59145232A
JPS59145232A JP2024683A JP2024683A JPS59145232A JP S59145232 A JPS59145232 A JP S59145232A JP 2024683 A JP2024683 A JP 2024683A JP 2024683 A JP2024683 A JP 2024683A JP S59145232 A JPS59145232 A JP S59145232A
Authority
JP
Japan
Prior art keywords
latex
polyolefin
sulfohalogenated
composition according
oxide
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
Application number
JP2024683A
Other languages
Japanese (ja)
Other versions
JPH0342300B2 (en
Inventor
Shuji Takagi
修治 高木
Ataru Mitsui
三井 中
Yoshitaka Ozaki
尾崎 好孝
Hidekazu Araki
英一 荒木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Seika Chemicals Co Ltd
Original Assignee
Seitetsu Kagaku Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Seitetsu Kagaku Co Ltd filed Critical Seitetsu Kagaku Co Ltd
Priority to JP2024683A priority Critical patent/JPS59145232A/en
Publication of JPS59145232A publication Critical patent/JPS59145232A/en
Publication of JPH0342300B2 publication Critical patent/JPH0342300B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:The titled composition which can be vulcanized after film formation, prepared by adding a metal oxide to a specified sulfohalogenated polyolefin latex. CONSTITUTION:An organic solvent solution of 100pts.wt. sulfohalogenated polyolefin (e.g., sulfochlorinated polyethylene) is dispersed in water in the presence of 0.1-20pts.wt. emulsifier (e.g., polyoxyethylene alkylphenyl ether sulfate ester salt), and the organic solvent is distilled off to obtain a sulfohalogenated polyolefin latex. This latex is mixed with an aqueous solution of 0.01-10pts.wt., per 100pts.wt. sulfohalogenated polyolefin, metal oxide (e.g., ZnO) and 0.01- 5pts.wt. vulcanization accelerator (e.g., tetramethylthiuram monosulfide) and the mixture is aged with stirring for about 24hr, cast on a support, and dried at 60 deg.C or above. The obtained film is vulcanized at 70-250 deg.C for several-about 30min.

Description

【発明の詳細な説明】 本発明は、スルホハロゲン化ポリオレフィンラテックス
組成物およびスルホハロゲン化ポリオレフィンラテック
スから得られた被1戻の加lute方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a sulfohalogenated polyolefin latex composition and a process for recursive addition obtained from the sulfohalogenated polyolefin latex.

スルホハロゲン化ポリオレフイノ(以下sHPとC各す
)、持に市販され【いるスルホクロル化ポリエチレンは
耐候゛注,*tオゾン′は,膚色安定往。
Sulfohalogenated polyolefins (hereinafter referred to as sHP and C), commercially available sulfochlorinated polyethylenes, are weather resistant;

朗炎性など柚々のすぐれた゛性質を・口し,谷柚ホース
類,屯線り1イlI+ 引布,ペイント、エスカレータ
−の手(Nなど、柚々の用途に使用され〔いる。これら
の用途に用い6Iこは、sHPv生ゴム配合による場合
もあるが、StiPを・η@溶f1こ俗解した俊、浸漬
.塗布,吹付などの方法で処理する場合もある。ところ
がこのようなイ11級溶故溶剤の状態で1史用すると、
中IJ.火災,公害など柚々の問題があり、それらの碓
点を同寸するため、ラテックスGEL(使用することが
要望さ」to〔いる。Sfi Pに+JJらず、−1役
にゴム力1はその→男性開力)ら使用IJυに/Jll
硫rる心安があるが,8に4Fラテツクスの)J11崎
」二つい(はこれまで殆んど知られていない。竹、(こ
成形後に加硫用油なSHPラテックスならびをこそれか
ら得られたf&膜を加硫する方法は全く知られていない
Taking advantage of the excellent properties of yuzu such as good flame resistance, yuzu is used for various purposes such as yuzuki hoses, liners, liners, paint, and escalator handles. In some cases, StiP is mixed with sHPv raw rubber, but in other cases, StiP is treated using methods such as dipping, coating, and spraying. When used for one period in the state of a class melting solvent,
Middle IJ. There are many problems such as fire and pollution, and in order to make these points the same size, it is recommended to use latex GEL. That→male opening force) to use IJυ/Jll
Although there is no need to worry about sulfurization, there is little known about the 8 and 4F latex J11 latex. There is no known method of vulcanizing f& films.

本発明者らは、StfPラテックスの加硫を二ついC 
Ill々杖tt・rの結果、St(Pの有懺溶剤浴液を
乳化剤の存在ト°ボ中に分散させ、i’i eat J
tF刑を留去し〔イミIたSt(Pラテックスを二特定
の加硫剤を配合して被膜形成俊をこ加(直LIJ− +
r目/:C S M Pラテックス組成物および該ラテ
ックスから得られたfJn I漠の〃l卸iE )j法
を見出した。
The present inventors conducted vulcanization of StfP latex in two C
As a result of tt・r, the solvent bath solution of St(P) was dispersed in the emulsifier-presence bottle, and i'i eat J
By distilling off the tF latex and adding a specific vulcanizing agent to the P latex, a film is formed.
We have found a method for producing a C S M P latex composition and fJn obtained from the latex.

叩ち本発明のSi(Pラテックス組成物は、sitPの
有機ポカリ溶液を乳化剤のイfー在F水中舎こ分散させ
、その後有機溶剤を留去して得たS H Pラテックス
Gこ加硫剤とLで少鼠の金属酸化物必要ならば加硫促進
剤の水分散液を添加した組成物であり、該液状組成物を
混合熟成し、60℃以上の温度で乾燥して被膜を形成し
、その後加熱することを9q畝とする被膜の加統方法で
ある。
The Si(P latex composition of the present invention is prepared by dispersing an organic Pocari solution of sitP in water containing an emulsifier and then distilling off the organic solvent.) It is a composition in which a small amount of metal oxide is added to the agent and L, if necessary, an aqueous dispersion of a vulcanization accelerator is added, and the liquid composition is mixed and aged, and dried at a temperature of 60°C or higher to form a film. This is a coating method in which 9q ridges are heated and then heated.

SHk’のラテックス化は、一般にS lI Pの有機
としてポリオキシエチレノンルビタン・モノラウレート
,ポリオキシエチレノソルビタノモノオレ主゛ート,ド
デシルフェニルポリグリコールエーテル。
Latexization of SHk' is generally performed using polyoxyethylenenon rubitan monolaurate, polyoxyethylene sorbitano monooleate, dodecylphenyl polyglycol ether as the organic material of SIP.

Q−19−Jレークーエチルウノデ刀ノーIレー4.−
1rfrWエステルl/2ソーダー塩,高分子カルホノ
甑エステルアル+Iレアリルボリエーテルアル」−ル,
46よび長鎖スルホン化アルコールならびをこ46分子
力ルホノ「稜やそれらJ)盆属8Aなどが便用でさるが
、とりDけ、ポリオキシエチレ/アルキルフェニルエー
テル艙酸エステル塩を用い〔乳化した場合には良好ノよ
ラテックスがイ:jしれる。
Q-19-J Reku Echiruunode Katana No I Rei 4. −
1rfrW ester l/2 soda salt, polymeric carphonokoshiki ester al+I realylbolyether al'-l,
46 and long-chain sulfonated alcohols and 46 molecular power fluorophores such as ridges and those J) Bongen 8A are used for convenience; If so, the latex will be in good condition.

ポリオキシエテレンアルキルフエニlレエーテル硫+i
グエステル塩とは一般式 〔ただL式中のR==炭、g数2〜20の炭化水素基、
n=l〜99(フェノール41モル1こ対するEOlの
」1ξ均付加セル数を表わす)、X=ナトリウム。
Polyoxyethylene alkyl phenylene ether sulfur +i
Guester salt is a general formula [R in the L formula = carbon, a hydrocarbon group with a g number of 2 to 20,
n=1 to 99 (representing the number of cells added in 1ξ of EOl to 1 mole of 41 phenol), X=sodium.

カリウムまたはアンモニウム)で表わされるポリオキシ
エチレンアlレキIレフエニlレエーテル争d酸エステ
ル塙であり、これらの単独、あるいは2曲以−Eを使用
することがでさり。
Polyoxyethylene alkylene ether (potassium or ammonium) is a polyoxyethylene alkylene ether diacetate ester, and these can be used alone or in combination.

ポリエテレンオキシドを構成するNoの11加モル数は
通常1〜99のものが便用できるが、好ましくは8〜5
0モル付加のものを使用すると灯結呆が得られることが
多い。
The number of moles of No added to 11 constituting the polyethylene oxide is usually conveniently 1 to 99, but preferably 8 to 5.
If a compound with 0 mole addition is used, a slag is often obtained.

乳化剤の便用縫は、スルホハロゲン化ポリオレフィン1
00爪琺rib Gこ刈L CO,1〜20重瀧都であ
る。便用敞がそれ以Fであると光分な乳化ができず、逆
にそれ以上使用し〔も経済上不利であるはかりでなく、
被I艮:17J性に悪影稀を及ぼす場合もあるなど有利
とはいえない。
The emulsifier is made of sulfohalogenated polyolefin 1.
00 Tsumekinrib G Kogari L CO, 1-20 Jutaki Miyako. If the useful oil is more than F, it will not be possible to emulsify light, and conversely, if it is used more than that, it will be economically disadvantageous.
Subject: 17J It cannot be said to be advantageous as it may have an adverse effect on the character.

不発明に使用する金属酸化物とは、酸化マダイ・シウム
、酸化亜鉛、−酸化鉛などの位属酸化物であり、これら
を単独または24々U以上混合して使用することができ
る。便用触はラテックス中の814P100重量都に対
しく、0.旧〜1))重は都、好ましくは0.1〜5重
量部、さらに好ましくは0.1〜2恵緘都である。
The metal oxides used in the invention are positional oxides such as red sea bream oxide, zinc oxide, and -lead oxide, and these can be used alone or in a mixture of 24 U or more. The toilet touch is 814P100 weight in latex, 0. 1) Weight is preferably 0.1 to 5 parts by weight, more preferably 0.1 to 2 parts by weight.

使用酸がこれ以上多くなると被1摸の形成が難しくなる
池、本来のSHPの特性を→I」うので好ましくなく、
辿をここれ以Fの少萌では光分な加硫を行なうことが難
しい。
If the amount of acid used is more than this, it will become difficult to form a SHP and the original characteristics of SHP will be affected, which is not desirable.
From this point on, it is difficult to perform optical vulcanization with a small amount of F.

加硫を行なう場合、通常、加硫促進剤を併用−1−るが
、5itpラテツクスの場合にも併用するのが好まL<
、例えばテトラメチルヂウラムモノスルフイド(’I’
SJ、テトラメチルチウフムジスルフィド(TMTiJ
Sハ ジペンタスチレンチウラムテトラスルフイド(T
RAJ等のチウラム系促進剤。
When performing vulcanization, a vulcanization accelerator is usually used in combination, but it is also preferable to use it in combination in the case of 5itp latex.
, for example, tetramethyldiuram monosulfide ('I'
SJ, tetramethylthiufum disulfide (TMTiJ
S Ha dipentastyrenethiuram tetrasulfide (T
Thiuram accelerators such as RAJ.

ジエチルチオウレア、ジフェニルチオウレア。Diethylthiourea, diphenylthiourea.

エチレンチ第1クレア等のチオウレア系促運剤カ使用で
きるが、ジチオカルバミン1投塩力1.チアゾール系等
の促進剤の併用もiJ 能である。
Thiourea-based promoters such as ethylene chloride can be used, but dithiocarbamin 1 salt dosage 1. The combined use of accelerators such as thiazoles is also effective.

加硫促進剤の使用量は、S )I P 100嵐縫部に
対し ’[11、旧〜5 爪F!c都、好ましくは0−
1〜27ki&やである。これより多いと製品が111
色しやすく、とれより少ないと効果が現われない。
The amount of vulcanization accelerator used is S) IP 100 storm seam part '[11, old ~ 5 nail F! c city, preferably 0-
1~27ki&ya. If there are more than this, the product will be 111
It is easy to color, and if it is less than the amount taken, the effect will not appear.

不発明で使用すasnPとは、エチレン、プロピレン、
m−ブチレノ、イソブチレン、ブタジェン、イソグレン
弄の単独重合体、これらと任意の2411以上の441
互共屯台体および、これらとエチリデンノルボーイ・ン
、5−メチルー2−ノルボーイ、ン、l、4−へ午サジ
エン、ジシクロペンタジェン。
asnP used for non-inventive purposes is ethylene, propylene,
Homopolymers of m-butylene, isobutylene, butadiene, isogrene, and any 2411 or higher 441
Mutual turrets and these together with ethylidene norboyne, 5-methyl-2-norboyne, l,4-hemo-sadiene, dicyclopentadiene.

1.5−シクロオクタジェノ、ジビニルベンゼンへ争の
非共役ジェノ類や、スチレン、塩化ビニル、酢flle
ビニル、7クリル1投、メタクリル1イ*、各t+ri
アクリル酸エステル類、各押メタクリル市エステル類等
との共重合体をハロゲンと二硫化硫黄または7Nロゲン
化スルフリルで処理し゛【生成したと考えられる(再漬
を口するポリマーであり、通常は適当なポリマーをスル
ホハUゲン化して製逍されたものを単独あるいは混合し
C使用する。ハロゲンとし調合方法としく5tlPGこ
対し0o01〜t o JICm sの加硫剤および心
安により0.O1〜51〜5恵緘都l硫促進剤を、加硫
剤または/JIJ (m促進創二水を、15〜40静二
85〜60部の調合で混合L’[水分散液にした俊、5
f(Pラテックスと混合する。水分散液の調製にはボー
ルミルなとを曲用−畳るっ水分散液は加硫剤、m硫促進
剤それぞれ単独に+i14裂した後、tys 疋績をS
HPラテックスと混合しても良(・L、加硫jIIIの
水分散液と〃11硫促進剤の水分散液とをあらかじめB
d合したものをSUPラテックスとj9tにの割合にな
るよう(こ混片しでもさしつかえ ゛ない。
1.5-cyclooctageno, divinylbenzene, non-conjugated genes, styrene, vinyl chloride, vinegar
Vinyl, 7kryl 1 throw, methacrylic 1i*, each t+ri
It is thought to be produced by treating copolymers with acrylic acid esters, various pressed methacrylic esters, etc. with halogen and sulfur disulfide or 7N sulfuryl halogenide. Polymers prepared by converting them into sulfohalogens are used alone or in combination.The halogen compounding method is 5tlPG, and the vulcanizing agent and safety range are 0.01 to 51 to 0.01 to JICms. 5. Mix the sulfur accelerator with a vulcanizing agent or /JIJ (m) in a mixture of 15 to 40 parts of 85 to 60 parts of sulfur accelerator L' [shun made into an aqueous dispersion, 5
f (mix with P latex. To prepare the aqueous dispersion, use a ball mill. After curing the aqueous dispersion with the vulcanizing agent and m vulcanization accelerator individually, add
It may be mixed with HP latex (L, the aqueous dispersion of vulcanized jIII and the aqueous dispersion of 11 sulfur accelerator are mixed in advance in B.
Mixed pieces should be in the same proportion as SUP latex and j9t (you can also use mixed pieces).

本発明組成物の加硫方法はS ri 、Pラテックスに
を加ん、攪拌しながら24時間熟成する。攪拌方法は従
来公知の方法をいずれも使用でき勾。熟成完了後組成物
をガラス板上に流延し、60℃以、Lの雰囲気トで被膜
を形成し、さら(こ形成したSHP未加硫被膜を70“
0〜250℃の温度で数分〜30分程度加硫するが、7
0℃〜250℃の温度で破LI’i”、形成と/111
硫、を同時に付なうこともできる。
The method of vulcanizing the composition of the present invention is to add S ri and P latex and age it for 24 hours while stirring. Any conventional stirring method can be used. After completion of aging, the composition was cast onto a glass plate, a film was formed at 60°C or higher in an atmosphere of L, and the formed SHP unvulcanized film was heated for 70
Vulcanize at a temperature of 0 to 250°C for a few minutes to 30 minutes, but
Break LI'i'' at temperatures between 0°C and 250°C, forming /111
Sulfuric acid can also be added at the same time.

本発明による81(t’ラテックス組成物は梃来公却の
方法でゴム引布剤、繊維加工剤、コーディング剤、jg
冶剤等をこ使用でき、すぐれた製品と/j L得る。
The 81(t' latex composition according to the present invention) can be used as a rubberizing agent, a fiber processing agent, a coating agent, a
You can use a lot of chemicals and get an excellent product.

不発す」のSHPラテックス徂J&物を二J9I宅によ
り父11i1’刑、補強ハ11.加工助剤、凹料寺従来
公知の配合聚晶を61S911することはIll &さ
しつかんない。
``Didn't explode'' SHP Latex Neighborhood J & Things 2 J9I's Father 11i1' Punishment, Reinforcement Ha 11. Processing aids and conventionally known combinations of 61S911 and 61S911 may not be used.

以ト、不発明の実施例を示すが、不発明はこれら(こ限
定されるものではない。
Hereinafter, examples of non-invention will be shown, but the invention is not limited to these.

なお、実施例中の部数はいずれも重敏部を表わすつ実施
VA&こおける各拙試我は以lこの如く行なった。
The numbers of copies in the Examples represent the critical parts, and the various tests in VA & Co. were carried out as follows.

引張り!11さ、伸び、モジュラス・・・JISK −
6:301に惺;拠し、シ3ツバ一式試躾43を用いて
、引張速度5 g 6 rom 、/分で行/ヨッタ。
Tension! 11 Strength, elongation, modulus...JISK -
At 06:301, using a three-piece collar set test training 43, a tensile speed of 5 g 6 rom / minute was carried out.

1[・・JIS K −6301に準拠して行ない、J
IS−Aタイプの硬度計を使用した。
1 [...Conducted in accordance with JIS K-6301, J
An IS-A type hardness meter was used.

実施例1 (スルホクロル化ポリエチレンラテックスの調製) ポリエチレン(密度0.96 g/c+n’ )より袈
逍したスルホクロル化ポリエチレン(塩g’S ’!J
t 85%。
Example 1 (Preparation of sulfochlorinated polyethylene latex) Sulfochlorinated polyethylene (salt g'S'!J) obtained from polyethylene (density 0.96 g/c+n')
t 85%.

碇黄含世1%)12■をトルエフロ8鞄に溶解した。Ikariko Goyo 1%) 12cm was dissolved in 8 bags of Tolueflo.

一刀、水+、oiw+こポリオキシエテレン(E、0゜
4モル付加ノオクチルフェニルエーテル硫酸エステ・レ
ソーダ鹿〔日本油JJ1j (体〕製、商品名トラック
スt(−45J ]、、22kg純分80%)と、ポリ
オキシエチレン(a、o、soモル付加ノノニルフエニ
・レエーテル硫酸エステルソーダー塩〔日本油Jlti
■装、商品名トラックスI”J−300)690g(純
が85%)と苛性カリ84gを1’4’f :;)> 
したちのを用意し、二つの溶液を乳化セー(特殊機化工
i佳硬′■゛、ベホモミ午す−ノで充分乳化した。
Itto, water +, OIW + polyoxyethylene (E, 0°4 mole addition of octyl phenyl ether sulfate ester, Resodaka [manufactured by Nippon Oil JJ1J (Body)], trade name TRAX T (-45J), 22 kg pure content 80%), polyoxyethylene (a, o, so mole addition nononylphenylether sulfate ester soda salt [NOF Jlti
690g (85% pure) and 84g of caustic potash for 1'4'f :;)>
Prepare a liquid and thoroughly emulsify the two solutions with an emulsifying solution (Special Machinery Chemical Industry Co., Ltd., Behomomi Usu-no).

このよう瘉こして+rtられた乳化液を2001のステ
アL/ス装の容器に移送L 150〜100+no+)
ig  の減圧ド、ジャ・fット部分蚤こ70Cの温ボ
をネ島環することをこより加熱し、トルエンノよどを留
去した。
Transfer the strained emulsion to a container equipped with a 2001 steer L/S.
The mixture was heated under reduced pressure in a 70°C vacuum cleaner to remove toluene and the like.

C賃却Iく、製品30kg+得た。製品の同形分は40
%であった。(以1;C8Mラテックスと帝すう(ty
W化マダマダイワム水分散液の調製〕”gυ(Ml )
            100fニオン系界面活LE
剤(註2)3 アンモニアカゼイン           8硅順ナト
リウム             0.5九屯    
水                        
         560.2(nI化唾鉛水分散液の
調装」 lnO(註8)      100 アニオン系界面活性剤     8 アンモニアカゼイン        3硅酸ナトリウム
        0.5純  水          
    148.5(加硫促進剤水分散液の調装) 加硫促進jT1100 アニオン系界面活性剤     8 1ンモニ7カゼイノ        8sIX   水
              144−ワマグ150〕 (註2) アニオン系界面活性剤〔花王アトラス社製1
曲品名:テモールI”J ) (註B)ZnU(正向化学■装、商品名:AZO)上記
組成で、Zllllll硫性促進剤の水分欣液をυ゛4
製し、衣−1の固形分組成でC8Mラテックスと混合し
20時間熟成し、組成物とした。これをガラス板上をこ
流姑した俊加熱乾燥し、さらに加熱加硫し被j漢形我後
、物性測定を行なった。
I got 30kg+ of product for rent. The same type of product is 40
%Met. (1; C8M latex and emperor (ty)
Preparation of W-treated Madamadaiwam aqueous dispersion〕”gυ(Ml)
100f ionic surfactant LE
Agent (Note 2) 3 Ammonia Casein 8 Sodium Sodium 0.59
water
560.2 (Preparation of nI salivary lead aqueous dispersion) lnO (Note 8) 100 Anionic surfactant 8 Ammonia casein Sodium trisilicate 0.5 Pure water
148.5 (Preparation of vulcanization accelerator aqueous dispersion) Vulcanization accelerator jT1100 Anionic surfactant 8 1 Nmoni 7 Caseino 8sIX Water 144-Wamag 150] (Note 2) Anionic surfactant [manufactured by Kao Atlas Co., Ltd. 1
Product name: Temor I"J) (Note B) ZnU (Masamukai Kagakusho, product name: AZO) With the above composition, add the water solution of Zllllll sulfuric accelerator to υ゛4
It was mixed with C8M latex with the solid content composition of batter-1 and aged for 20 hours to obtain a composition. This was dried on a glass plate under low heat, then heated and vulcanized, and the physical properties were measured.

七の結果を下衣−2,および3Gこ承す。なお、表−2
は被膜乾燥条件70°C×3時間、加硫条[+140℃
X20分であり、表−8は被膜乾燥条件70℃×3時間
、加蝋条件200℃×3分である。
Accept the results of 7, 2 and 3G. Furthermore, Table 2
is film drying condition 70°C x 3 hours, vulcanized strip [+140°C
Table 8 shows the coating drying conditions: 70°C x 3 hours, and the waxing conditions: 200°C x 3 minutes.

表 −1 衣  −2 表−8 実施例2 (−酸化縮水分散液の調製〕 pbu  (註4 )       100デモールN
3 アンモニアカゼイン     3 硅Cfiナトリウム    0.5 純        水    198.5−(酸化マグ
ネシウム水分散液のKQJM)・・・・・・実施例1と
同じ (加艙促進/ll水分1枚液の調製)・・・・・・実施
例1と同じ(吐4.)PbU(市川化工■製、商品名:
リサージ〕フロピレン(SC)’Pノラテックス、スI
レホクロル化エチレンプロピレンジエン共重合物(5C
EPIIVI)ラテックスと混合し、20時間熟成した
秋ガラス板上に流媛し、70℃で371守1iiJ を
陀kl俊14 f) ’Cで20分〃11硫し、物′往
n111定を行なった。・Cの結果を表−5に示響−0 表 −5 出顧人製鉄化学上末体式会社 代表番 佐々木  清
Table-1 Clothing-2 Table-8 Example 2 (-Preparation of oxidized condensed water dispersion) pbu (Note 4) 100 demole N
3 Ammonia casein 3 Sodium Cfi 0.5 Pure water 198.5- (KQJM of magnesium oxide aqueous dispersion) Same as Example 1 (promotion of heating/preparation of 1 l water solution) ...Same as Example 1 (4.) PbU (manufactured by Ichikawa Kako ■, product name:
Resurge] Flopylene (SC)'P Noratex, SC I
Rehochlorinated ethylene propylene diene copolymer (5C
EPIII) Mixed with latex, aged for 20 hours, poured onto a glass plate, sulfurized at 70°C for 20 minutes, and determined. Ta.・The results of C are shown in Table-5.

Claims (1)

【特許請求の範囲】 (IJ  スルホハロゲン化ポリオレフィンの有機溶剤
溶液を乳化剤の存在F水中に分散させ、その後M機浴剤
を置去L−C得たスルホ/’%ログン化ポリオレフィン
ラテックスに、金属酸化物の少なくともl柚を該ラテッ
クス中のスルホハロゲン化ポリオレフィン100車社都
をこ対し0.O1〜10車量都添加混合しくなるスルホ
ハロゲン化ポリオレフイノラテックス#11戊物。 (2)  スルホハロゲン化ポリオレフ1ンフテツクス
がスルホクロル る待11f i+#求の範囲(1)記載の組成物。 (8)  スルホハロゲン化ポリオレフィンラテックス
がスlレホクロル化ボリフ゛口とレンラテックスである
特許請求の範囲(1)記載の組成物。 (4)  スルホハロゲン化ポリオレフィンラテックス
がスルホクロル化エチレンプロとレンジエンコポリマー
である符if請求の範囲(1)記載の組成物つ(5) 
 乳化剤としCポリオキシエチレンアル午ルフェニルエ
ーテルi1Mエステル塩の少なくと61便を用いる特.
f[請求の範囲(1)記載の組成物。 (67  ホリオキシエチレンアルキルフェニルエーテ
ル硫酸エステル塩をスルホハロゲン化ポリオレフィン1
00嵐量都(二対して0.1〜woIii仕都使用する
特許請求の範囲(9記載の嬉欧 (7)  金属v貨化物が酸化マダイ・シウムである将
a’f請求の範囲(11記載の組成物。 (8)  金属酸化物が酸化亜鉛である特許請求の範囲
(1)−俄の組成物。 (9)  スルホハロゲン化ポリオレフィンの有機浴剤
浴液を乳化剤の存在ド水中に分散させ、その後ホハロゲ
ン化ポリオレフインラテツクMO’c、以上の温度で乾
燥して得られた被膜を加熱することを特徴とVるスlレ
ホハロゲン化ポリオレフィンラテックスから肖られた被
膜の加硫方法。 (10)スJレホハロゲン化ポリオレフィンラテックス
がスルホクロル化ポリエチレンラテックスである竹計r
jl’J求1.Q範囲(9)記載の方法。 (ll)スルホハロゲン化ポリオレフィンラテックスが
スルホクロル化ポリフロピレンラテックスである特許請
求の範囲(9)記載の井硫方法。 (12)スルホハロゲン化ポリオレフィンラテックスが
スルホクロル ポリマーラテックスである特許請求の範囲(9)記載方
法。 (18)乳化剤としてポリオキシエチレンアルキルフェ
ニルエーテル4Jff.、Wエステル塩の少なくとモl
f4+を用いる待1汗請求の範囲(9)記載の方法。 (14)ポリオキシエテレンアルキルフエニルエーテl
し疎目iエステルフjiをスルホハロゲン化ポリスレフ
イノioo屯11こ対し’[0.1〜20 Jf軟軟便
使用る特許請求の範囲(I3)記載の方法つ(15)金
/,n#化゛吻が酸化マグネシウムである待r「請求の
範囲(9)記載の方法。 (16)被腐酸化物が酸化所飴であ6待♂[請求の範囲
(9)記載の方法。
[Scope of Claims] (IJ An organic solvent solution of a sulfohalogenated polyolefin is dispersed in F water in the presence of an emulsifier, and then a M bath agent is left behind. The sulfohalogenated polyolefin latex #11 is mixed with at least 1 liter of oxide in an amount of 0.01 to 10 mol per 100 ml of the sulfohalogenated polyolefin in the latex. (2) The composition according to claim (1), wherein the halogenated polyolefin latex is a sulfochlorinated polyolefin latex. (8) The composition according to claim (1), wherein the sulfohalogenated polyolefin latex is a sulfochlorinated polyolefin latex. (4) If the sulfohalogenated polyolefin latex is a sulfochlorinated ethylene pro-diene copolymer, the composition according to claim (1) (5)
A special method using at least 61% of C polyoxyethylene alkyl phenyl ether i 1M ester salt as an emulsifier.
f [The composition according to claim (1). (67 Polyoxyethylene alkyl phenyl ether sulfate sulfohalogenated polyolefin 1
Claims (7) in which the metal v cargo is red sea bream oxide (11) The composition according to claim 1. (8) The composition according to claim 1, wherein the metal oxide is zinc oxide. (9) An organic bath solution of sulfohalogenated polyolefin is dispersed in water in the presence of an emulsifier. A method for vulcanizing a film made from a halogenated polyolefin latex, characterized by heating the film obtained by drying the halogenated polyolefin latex at a temperature higher than MO'c (10). ) SJ Rehohalogenated polyolefin latex is sulfochlorinated polyethylene latex
jl'J 1. The method described in Q range (9). (11) The method according to claim (9), wherein the sulfohalogenated polyolefin latex is a sulfochlorinated polypropylene latex. (12) The method described in claim (9), wherein the sulfohalogenated polyolefin latex is a sulfochloropolymer latex. (18) Polyoxyethylene alkyl phenyl ether 4Jff. as an emulsifier. , at least mol of W ester salt
The method according to claim (9) using f4+. (14) Polyoxyethylene alkyl phenyl ether
The process according to claim (I3), which uses sulfohalogenated polysulfinyl ester fluoride with 0.1 to 20 Jf soft stool (15) Gold/, n# (16) The method according to claim (9), wherein the oxide to be corroded is magnesium oxide.
JP2024683A 1983-02-08 1983-02-08 Sulfohalogenated polyolefin latex composition and vulcanization of film prepared therefrom Granted JPS59145232A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2024683A JPS59145232A (en) 1983-02-08 1983-02-08 Sulfohalogenated polyolefin latex composition and vulcanization of film prepared therefrom

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2024683A JPS59145232A (en) 1983-02-08 1983-02-08 Sulfohalogenated polyolefin latex composition and vulcanization of film prepared therefrom

Publications (2)

Publication Number Publication Date
JPS59145232A true JPS59145232A (en) 1984-08-20
JPH0342300B2 JPH0342300B2 (en) 1991-06-26

Family

ID=12021832

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2024683A Granted JPS59145232A (en) 1983-02-08 1983-02-08 Sulfohalogenated polyolefin latex composition and vulcanization of film prepared therefrom

Country Status (1)

Country Link
JP (1) JPS59145232A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0306120A2 (en) * 1987-08-11 1989-03-08 Tosoh Corporation Chlorosulfonated ethylene.alpha-olefin copolymer composition and process for the production thereof
WO2012141020A1 (en) * 2011-04-11 2012-10-18 住友精化株式会社 Chlorosulfonated polyethylene latex

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0306120A2 (en) * 1987-08-11 1989-03-08 Tosoh Corporation Chlorosulfonated ethylene.alpha-olefin copolymer composition and process for the production thereof
WO2012141020A1 (en) * 2011-04-11 2012-10-18 住友精化株式会社 Chlorosulfonated polyethylene latex
JP5890950B2 (en) * 2011-04-11 2016-03-22 住友精化株式会社 Chlorosulfonated polyethylene latex
US9695298B2 (en) 2011-04-11 2017-07-04 Sumitomo Seika Chemicals Co., Ltd. Chlorosulfonated polyethylene latex

Also Published As

Publication number Publication date
JPH0342300B2 (en) 1991-06-26

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