JPH0248003B2 - PEESUTOKAKOYOENKABINIRUJUSHINOKAISHUHOHO - Google Patents

PEESUTOKAKOYOENKABINIRUJUSHINOKAISHUHOHO

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Publication number
JPH0248003B2
JPH0248003B2 JP22089882A JP22089882A JPH0248003B2 JP H0248003 B2 JPH0248003 B2 JP H0248003B2 JP 22089882 A JP22089882 A JP 22089882A JP 22089882 A JP22089882 A JP 22089882A JP H0248003 B2 JPH0248003 B2 JP H0248003B2
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Japan
Prior art keywords
resin
vinyl chloride
chloride resin
weight
aqueous dispersion
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JP22089882A
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Japanese (ja)
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JPS59109504A (en
Inventor
Masaaki Nishina
Eitaro Nakamura
Junichi Watanabe
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Zeon Corp
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Nippon Zeon Co Ltd
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Priority to JP22089882A priority Critical patent/JPH0248003B2/en
Publication of JPS59109504A publication Critical patent/JPS59109504A/en
Publication of JPH0248003B2 publication Critical patent/JPH0248003B2/en
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Description

【発明の詳现な説明】 本発明は、ペヌスト加工に䟛される粒状の塩化
ビニル暹脂の補造方法に関する。 通垞塩化ビニル暹脂をペヌスト加工するに際し
おは、ペヌスト加工甚に補造された塩化ビニル暹
脂以䞋暹脂ずいうこずがあるを、可塑剀、安
定剀の他、必芁に応じお顔料、充おん剀等の配合
剀ずずもに混合し液状のプラスチゟルずし、成圢
工皋ぞ䟛する方法が採られる。そしお液状のプラ
スチゟルを泚圢、コヌテむング、浞挬等の手段で
賊型し、加熱溶融固化させるこずによ぀お成圢品
を埗る。埓぀お、プラスチゟルの流動特性はペヌ
スト加工の成圢性に極めお重芁な圱響を及がす特
性であるため、配合凊方䞊、ずりわけ暹脂の品質
蚭蚈䞊、倚倧な努力ず工倫が斜されおいるのが実
情である。䞀般には、そのための暹脂の補造方法
ずしおは、塩化ビニル又は塩化ビニルを䞻䜓ずす
る単量䜓混合物をラゞカル発生型重合開始剀ず乳
化剀の存圚䞋、乳化重合あるいは懞濁重合するこ
ずによ぀お粒埄0.05〜5Όの球型暹脂の氎性分散を
埗、この氎性分散液をスプレヌ也燥する方法が採
られおいる。 ずころがこうした方法で埗られた暹脂は、暹脂
の氎性分散液䞭の党おの䞍揮発成分を含んでお
り、成圢品の熱安定性、耐氎性、透明性等の特性
を䜎䞋させる原因ずな぀おいる。さらに、通垞の
スプレヌ也燥では、噎霧された氎分散液䞭の暹脂
粒子は、氎分の蒞発に䌎぀お暹脂粒子が匷固な集
合䜓ずしお也燥、捕捉されるため、補品ずしお出
荷するためには粉砕工皋を芁する堎合があるし、
こうした凊理を行぀おもプラスチゟル補造時の簡
単な混合では集合粒子の分散を達成できないこず
が倚い。さらに、埓来の暹脂は埮现な粉䜓である
ため、補品の袋詰め時、䞊びにプラスチゟル補造
に際しおの開袋投入及び混合時の粉䜓飛散等、䜜
業環境の䜎䞋を匕き起こすばかりでなく、粉䜓流
動性が悪いため、自動蚈量、自動茞送が困難であ
る。 本発明者は、こうしたペヌスト加工甚塩化ビニ
ル暹脂の珟状の問題点に぀いお怜蚎した結果、ペ
ヌスト加工甚塩化ビニル暹脂の氎性分散液に、氎
に難溶であ぀おか぀該塩化ビニル暹脂を溶解又は
膚最させない有機液䜓を添加しお混合するこずに
より、塩化ビニル暹脂を粒状集合䜓ずしお氎盞よ
り分離せしめた埌也燥するこずによ぀お、粉䜓ず
しおの流動性が良奜で飛散性が少なく、プラスチ
ゟルずしたずきには、十分ペヌスト加工に䟛し埗
る分散性ず䜎粘床性を有し、か぀優れた熱安定
性、耐氎性、透明性を有する成圢品を䞎える粒状
塩化ビニル暹脂が回収できるこずを先に芋い出し
おいる。 しかし、この方法の効率を䞀段ず向䞊させるべ
く、曎に怜蚎を重ねた結果、䞊蚘塩化ビニル暹脂
に、特定の粒埄の塩化ビニル暹脂を特定量䜵甚す
るこずにより暹脂が極めお高い効率で埗られ、曎
には、粒状集合䜓を分離した埌の氎盞䞭に含たれ
る暹脂分の回収が極めお容易であるこずを確認
し、本発明を完成するに至぀た。 すなわち本発明は、ペヌスト加工甚塩化ビニル
暹脂の氎性分散液に、氎に難溶であ぀おか぀該塩
化ビニル暹脂を溶解又は膚最させない有機液䜓を
添加しお混合するこずにより、塩化ビニル暹脂を
粒状集合䜓ずしお氎盞より分離せしめた埌也燥す
るこずによ぀お、塩化ビニル暹脂を回収するに際
し、ペヌスト加工甚塩化ビニル暹脂の氎性分散液
に、平均粒埄が10〜60ミクロンの範囲の粗倧塩化
ビニル暹脂を、党暹脂量䞭〜70重量、奜たし
くは〜60重量ずなる範囲で添加するこずを特
城ずするペヌスト加工甚塩化ビニル暹脂の回収方
法に関するものである。 本発明の方法は、以䞋に瀺す基本的な工皋、す
なわち、(1)暹脂の氎性分散液ず有機液䜓ずを混合
し、暹脂を有機液䜓を介しお集合せしめる第工
皋、(2)第工皋で埗られた暹脂集合䜓を含む混合
液から氎盞を分離陀去する第工皋、(3)氎盞を陀
去した暹脂集合䜓を也燥する第工皋、曎に必芁
に応じお(4)第工皋で分離された氎盞䞭の暹脂を
第工皋で䜿甚する原料に混合する第工皋で構
成されおいる。 本発明においお甚いられるペヌスト加工甚塩化
ビニル暹脂平均粒埄は0.05〜5Όの氎性分散液
及び平均粒埄10〜60ミクロンの塩化ビニル暹脂
以䞋粗倧塩化ビニル暹脂ずいうこずがあるは、
通垞の乳化重合又は懞濁重合により補造された塩
化ビニル暹脂の単独重合䜓又は塩化ビニルを䞻䜓
ずし通垞は70重量以䞊、これず酢酞ビニル、
塩化ビニリデン、゚チレン、プロピレン、ブテ
ン、アクリロニトリル、アクリル酞゚ステル、メ
タクリル酞゚ステル又はマレむン酞などのオレフ
むン系単量䜓ずの共重合䜓を、その暹脂組成ずし
お有するものである。 粗倧塩化ビニル暹脂ずしおは、重合埌の氎分散
液、脱氎埌のり゚ツトケヌキ、也燥埌の粉末暹脂
のいずれを甚いおもよいが、粗倧塩化ビニル暹脂
添加埌の氎性分散液䞭の党塩化ビニル暹脂の含量
が10〜70重量であるこずが望たしい。10重量
未満の堎合は廃氎量が補品量に比し、倚くなり過
ぎる結果䞍経枈であり、70重量を越える堎合に
は、氎性分散液ず有機液䜓の混合物の粘床が著し
く䞊昇しおしたうため、操業が困難ずなる。た
た、粗倧塩化ビニル暹脂の平均粒埄が60ミクロン
を越えるず、薄膜コヌテむング加工時の筋匕きや
成圢品衚面の荒れ、艶消しなどを匕き起こし奜た
しくない。又、10ミクロン未満になるず粒状塩化
ビニル暹脂の回収効率、分離氎からの暹脂分の回
収効率が䜎䞋する。又、粗倧塩化ビニル暹脂の添
加量が重量未満の堎合、暹脂の回収性、ゟル
ずしたずきの粘床特性が䞍良ずなり、䞀方70重量
を越えお堎合、暹脂の回収効率の向䞊、分離氎
からの暹脂分の回収の容易さは保たれるが、埗ら
れた補品をプラスチゟルにしおペヌスト加工に䟛
した堎合、ゲル化性の䜎䞋、成圢品の機械的匷床
の䜎䞋が倧きくなる為、甚途範囲が限定されおし
たう欠点が生じる。 塩化ビニル暹脂の氎性分散液に添加される有機
液䜓は、氎に難溶であ぀お、か぀本発明における
分離回収時においおは暹脂を溶解又は膚最しない
ものである。䞀般的にはこの有機液䜓ずしおは、
融点が20℃以䞋、垞圧における沞点が本発明の分
離回収時の枩床以䞊、奜たしくは200℃以䞊のも
のがいられる。有機液䜓ずしお沞点が分離回収時
の枩床未満のものを甚いた堎合には、これが揮散
するためこの回収に付加蚭備を芁し経枈的でな
い。むろん、単品ずしおは、以䞊に述べた条件を
倖れるものであ぀おも混合物ずしお䞊述した芁件
を備えおいるものであれば良い。 有機液䜓が氎に難溶であるこずが芁求される理
由は以䞋の点にある。第には、氎性分散液ず
の混合のあず、分離すべき氎盞ぞの同䌎量を枛少
させお、有機液䜓の損倱を防ぎ、廃氎凊理費甚を
軜枛させるためであり、第には、氎に分散した
暹脂粒子を有機液䜓を介しお集合せしめるには、
暹脂粒子ず氎ずの間に有機液䜓が界面を持぀た液
盞ずしお存圚するこずが必芁であるためである。
たた、甚いる有機液䜓が、本発明における分離回
収時の枩床においお暹脂を溶解又は膚最させるも
のである堎合には、暹脂粒子が倉圢、倉質を起こ
すため䞍郜合である。なお、本発明で䜿甚した有
機液䜓は倧郚分が補品暹脂に残留するため、ペヌ
スト加工時の操䜜性、加工性および成圢品の品質
に察し悪圱響を䞎えるものは避けなければならな
い。以䞊の点からすれば、有機液䜓ずしお通垞ペ
ヌスト加工に甚いられる液状配合剀を䜿甚するの
が䞀番自然で合理的である。 本発明における有機液䜓の䟋ずしおは以䞋の様
なものが挙げられる。 (1) ゞオクチルフタレヌト、ゞノニルフタレヌ
ト、ブチルラりリルフタレヌト、メチルオレむ
ルフタレヌト等のフタル酞アルキル゚ステル系
可塑剀 (2) トリオクチルトリメリテヌト、ゞ゚チレング
リコヌルゞベンゟ゚ヌト等の芳銙族カルボン酞
゚ステル系可塑剀 (3) ゞオクチルアゞペヌト、ゞブチルセバケヌ
ト、ゞオクチルテトラヒドロフタレヌト等の脂
肪族二塩基酞゚ステル系可塑剀 (4) トリオクチルフオスプヌト、トリクロロ゚
チルフオスプヌト等のリン酞゚ステル系可塑
剀 (5) ゞ゚チレングリコヌルゞカブリレヌト、1.4
ブチレングリコヌル−ゞ−−゚チルヘキサノ
゚ヌト等の脂肪酞グリコヌル゚ステル系可塑剀 (6) ポリ゚ステル系可塑剀 (7) オレむン酞ブチル、アセチルリシノヌル酞メ
チル、、−トリメチル−、−ペンタ
ンゞオヌルゞむ゜プチレヌト等の脂肪酞゚ステ
ル系、゚ポキシ化倧豆油、゚ポキシステアリン
酞オクチル等の゚ポキシ系、塩玠化脂肪酞メチ
ル、塩玠化パラフむン等の塩玠化パラフむン
系、コハク酞ゞオクチル等の脂肪族二塩基酞゚
ステル系の二次可塑剀 (8) ミネラルスピリツト、ミネラルタヌペン等の
石油系、ドデシルベンれン等の長鎖アルキルベ
ンれン系の垌釈剀 (9) 高玚アルコヌル、流動パラフむン、高玚脂肪
酞アルキル゚ステル等の液状滑剀 有機液䜓の添加量は、氎性分散液䞭の暹脂100
重量郚に察し、0.5〜20重量郚、奜たしくは〜
15重量郚の範囲で遞定すべきである。該添加量が
20重量郚を越えるず、所望の粒状物が埗られずゟ
ル状物が生成する堎合が起こり埗る。たずえ、粒
状物が埗られたずしおも、有機液䜓の含有量が倧
きい為に埌段の也燥工皋での氎分の陀去が困難に
なる恐れがある。該添加量が0.5重量郚未満では、
所望の粒状物はほずんど埗られない。 有機液䜓ず暹脂の氎性分散液ずの混合は、20〜
70℃、奜たしくは、20〜50℃の範囲で行なうべき
である。該枩床が70℃を越えるず、有機液䜓によ
る暹脂の膚最、吞収が促進され、か぀、暹脂の軟
化による合䜓も起こり始める為に、最終補品の分
散性を著しく損なう危険性がある。 有機液䜓ず暹脂の氎性分散液を混合する方法ず
しおは、公知の方法が採甚できるが、混合の皋床
は暹脂の有機液䜓による集合胜率に倧きな圱響を
䞎えるため、奜たしくは混合装眮の単䜍容積圓り
の混合動力が1KWM3立方メヌトル圓り
キロワツト以䞊であ぀お、混合時間ずの積が、
4KW・HrM3以䞊であるようにすべきである。
混合装眮ずしおは混合の均䞀性、連続性などの点
から、高速回転匏連続混合機や倚翌型連続混合槜
の䜿甚が奜たしいが、通垞の撹拌槜型の混合機や
静䞊型混合噚も䜿甚し埗る。 次に有機液䜓を介しお集合した暹脂集合䜓から
氎盞を分離するには、捕捉された暹脂混合物の圢
状に応じお、公知の法を甚いれば良い。ただし、
暹脂の軟化、合䜓を防ぐために枩床は20〜70℃の
範囲ずしなければならない。 分離工皋にお分離された暹脂粒子は、次に也燥
工皋に送られ、有機液䜓ず付着氎分が陀去され
る。この也燥工皋においおは、広く公知の也燥装
眮が䜿甚可胜であるが、暹脂の集合、合䜓の匷床
がペヌスト加工時の分散性を損なわぬ様な条件を
蚭定するこずが必芁である。すなわち也燥工皋䞭
の被也燥暹脂の枩床は70℃以䞋、奜たしくは50℃
以䞋ずなる様にする。 このようにしお塩化ビニル暹脂が高収率で埗ら
れるが、このものは流動性が良奜で飛散性が少な
く、しかも垞法によりプラスチゟルずしたずきの
粘床特性や成圢品ずしたずきの熱安定性等の物性
も優れおいる。 次に実斜䟋により本発明の方法を説明する。な
お、塩化ビニル暹脂の平均粒埄は、暹脂粒子の重
量分垃で50の点の粒埄を瀺す。たた、粒状塩化
ビニル暹脂の回収効率は䞋蚘匏により算出した。 回収効率所定の目開きの金網䞊に篩分けられた塩化
ビニル暹脂の重量仕蟌たれた塩化ビニルラテツクス䞭
の塩化ビニル暹脂の重量×100 たた、暹脂の沈降性、粉䜓性、ゟル暹脂50
ずゞ−−゚チルヘキシルフタレヌト30ずをら
いかい機で混合しお調補したもの特性及びフむ
ルム特性に぀いお䞋蚘に説明する。 スクリヌン通過埌の分離氎䞭の暹脂の沈降性 分離氎をガラス容噚に採取しお静眮した埌、
〜分以内にほが透明な䞊柄液が生成する堎合を
良奜、10分埌でも䞊柄液が生じないものを䞍良ず
する。 安息角 粉䜓の流動し易さを瀺すもので数倀が小さいほ
どの流動性に優れる。 かさ比重 粉䜓の芋掛の密床であ぀お、倧きい数倀である
ほど取扱い性が良奜である。 付着性 詊料を玙の䞊に眮き氎平に振動させた埌詊料を
捚おお玙䞊に付着した暹脂量の倚少を芳察する。
少ないほど良い。 粘 床 ブルツクフむヌルドBM型粘床蚈ロヌタヌ
により6rpmで枬定したずき初日、及び23℃で
日間攟眮したずき日埌のゟル枩23℃での
倀。 ノヌスフアむネス ゟル䞭の暹脂粒子の粒床を瀺すもので、数倀が
倧きい皋现かいが最も现かくが最も荒い。 熱安定性 ゟルをアルミニりム補モヌルドに泚入し、190
℃の熱颚雰囲気䞋で30分埌の色調の倉化を倉
化小〜倉化倧の段階で衚瀺する。 フむルム匷床 ゟルを厚みmmのガラス板䞊に400Ό厚みでコ
ヌテむングし、180℃の熱颚雰囲気䞋で10分間加
熱ゲル化しおフむルムを成圢し、JIS −6301−
75準拠の号ダンベルずしお、匕匵速床200mm
minでの砎断時匕匵匷床を枬定する。 実斜䟋  ペヌスト加工甚塩化ビニル暹脂の氎性分散液
固圢分含量30重量、平均粒埄1.2Ό3000、
45Όの平均粒埄を有する粗倧塩化ビニル暹脂の氎
性分散液固圢分含量30重量400及びゞ−
−゚チルヘキシルフタレヌト61を、内郚に盎
埄cmの倚数の撹拌翌を持぀内埄10cm、内容積
3.8の円筒型ステンレス補混合機に入れ、
1200rpmで10分間混合したずころ、球状暹脂組成
物の氎分散液が埗られた。この分散液から60メツ
シナの金網で球状暹脂組成物を分離し、金網䞊の
ものを遠心脱氎したずころ826の湿最粒状物が
埗られた。これを熱颚匏也燥機内35℃で12時間也
燥させたずころ603の暹脂(A)が埗られた。 実斜䟋  ペヌスト加工甚塩化ビニル暹脂の氎性分散液
固圢分含量30重量、平均粒埄1.2Ό3200、
26Όの平均粒埄を有する粗倧塩化ビニル暹脂粉末
300及びゞ−−゚チルヘキシルフタレヌト100
を1000rpmで15分間混合した以倖は、実斜䟋
ず党く同様の装眮・手順で実隓を行な぀た。埗ら
れた湿最粒状物の重量は1170、也燥暹脂(B)の重
量は831であ぀た。 比范䟋  実斜䟋で甚いたペヌスト加工甚塩化ビニル暹
脂の氎性分散液固圢分含量30重量3400ず
ゞ−−゚チルヘキシルフタレヌト61を甚いお
実斜䟋ず党く同様の装眮・条件・手順で実隓を
行な぀た。埗られた湿最粒状物の重量は402、
也燥暹脂(C)の重量は285であ぀た。 比范䟋  実斜䟋で甚いたペヌスト加工甚塩化ビニル暹
脂の氎性分散液ただし固圢分含量は15重量に
調敎2600、粗倧塩化ビニル暹脂粉末800及
びゞ−−゚チルヘキシルフタレヌト95を甚い
お、実斜䟋ず党く同じ装眮・条件・手順で実隓
を行぀た。埗られた湿最重量物の重量は1060、
也燥暹脂(D)の重量は785であ぀た。 比范䟋  実斜䟋で甚いたペヌスト加工甚塩化ビニル暹
脂の氎性分散液固圢分含量30重量3000、
93Όの平均粒埄を有する粗倧塩化ビニル暹脂の氎
性分散液固圢分含量32重量500及びゞ−
−゚チルヘキシルフタレヌト64を甚いお、実
斜䟋ず党く同様の装眮、条件、手順で実隓を行
぀た。埗られた湿最粒状物の重量は866、也燥
暹脂(E)の重量は632であ぀た。 参考䟋  実斜䟋で甚いたペヌスト加工甚塩化ビニル暹
脂の氎性分散液をスプレヌ也燥機により、入口枩
床160℃、出口枩床56℃で也燥し、卓䞊パルベラ
むザヌで粉砕しお、也燥暹脂(F)を埗た。 衚に(A)〜(F)の暹脂の回収効率及び特性等を瀺
す。 【衚】
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing granular vinyl chloride resin to be subjected to paste processing. Normally, when paste processing vinyl chloride resin, the vinyl chloride resin (hereinafter referred to as resin) manufactured for paste processing is mixed with plasticizers, stabilizers, pigments, fillers, etc. as necessary. A method is adopted in which the plastisol is mixed with an agent to form a liquid plastisol and then subjected to a molding process. Then, the liquid plastisol is shaped by means such as casting, coating, dipping, etc., and a molded article is obtained by heating and melting and solidifying the plastisol. Therefore, the fluidity properties of plastisol are properties that have an extremely important effect on the formability of paste processing, and the reality is that great effort and ingenuity are put into the formulation, especially in the quality design of the resin. be. Generally, the method for producing resin for this purpose involves emulsion polymerization or suspension polymerization of vinyl chloride or a monomer mixture mainly composed of vinyl chloride in the presence of a radical-generating polymerization initiator and an emulsifier. A method has been adopted in which an aqueous dispersion of spherical resin having a diameter of 0.05 to 5 ÎŒm is obtained and this aqueous dispersion is spray-dried. However, the resin obtained by this method contains all the nonvolatile components in the aqueous resin dispersion, which causes a decrease in properties such as thermal stability, water resistance, and transparency of the molded product. Furthermore, in normal spray drying, the resin particles in the sprayed aqueous dispersion are dried and captured as a solid aggregate as the water evaporates, so a pulverization process is required to ship the product. It may require
Even with such treatments, it is often impossible to achieve dispersion of aggregated particles by simple mixing during plastisol production. Furthermore, since conventional resins are fine powders, they not only cause a deterioration of the working environment, such as powder scattering when products are packed into bags or when opened and mixed during plastisol production, but also cause powder flow. Due to poor performance, automatic weighing and transportation are difficult. As a result of studying the current problems of the vinyl chloride resin for paste processing, the present inventor found that the vinyl chloride resin is difficult to dissolve in water and can be dissolved or swollen in an aqueous dispersion of the vinyl chloride resin for paste processing. By adding and mixing an organic liquid that does not cause oxidation, the vinyl chloride resin is separated from the aqueous phase as a granular aggregate, and then dried, resulting in a powder with good fluidity and little scattering, and is similar to plastisol. We have previously discovered that when this process is carried out, it is possible to recover granular vinyl chloride resin that has sufficient dispersibility and low viscosity to be subjected to paste processing, and which provides molded products with excellent thermal stability, water resistance, and transparency. . However, in order to further improve the efficiency of this method, as a result of further studies, we found that by combining the above vinyl chloride resin with a specific amount of vinyl chloride resin of a specific particle size, a resin can be obtained with extremely high efficiency. confirmed that it is extremely easy to recover the resin contained in the aqueous phase after separating the granular aggregates, and completed the present invention. That is, the present invention makes the vinyl chloride resin granular by adding and mixing an organic liquid that is sparingly soluble in water and does not dissolve or swell the vinyl chloride resin into an aqueous dispersion of the vinyl chloride resin for paste processing. When recovering vinyl chloride resin by separating it from the aqueous phase as an aggregate and drying it, coarse chloride with an average particle size in the range of 10 to 60 microns is added to the aqueous dispersion of vinyl chloride resin for paste processing. The present invention relates to a method for recovering vinyl chloride resin for paste processing, characterized in that vinyl resin is added in an amount of 1 to 70% by weight, preferably 5 to 60% by weight based on the total amount of resin. The method of the present invention consists of the following basic steps: (1) a first step of mixing an aqueous resin dispersion and an organic liquid and aggregating the resin via the organic liquid; A second step of separating and removing the aqueous phase from the mixed liquid containing the resin aggregate obtained in the step, (3) a third step of drying the resin aggregate from which the aqueous phase has been removed, and (4) a further step as necessary. The fourth step consists of mixing the resin in the aqueous phase separated in the second step with the raw material used in the first step. The aqueous dispersion of vinyl chloride resin for paste processing (average particle size: 0.05 to 5 ÎŒm) and vinyl chloride resin (hereinafter referred to as coarse vinyl chloride resin) having an average particle size of 10 to 60 ÎŒm used in the present invention are:
A vinyl chloride resin homopolymer or vinyl chloride produced by normal emulsion polymerization or suspension polymerization (usually 70% by weight or more), and vinyl acetate,
Its resin composition is a copolymer with an olefinic monomer such as vinylidene chloride, ethylene, propylene, butene, acrylonitrile, acrylic ester, methacrylic ester, or maleic acid. As the coarse vinyl chloride resin, any of an aqueous dispersion after polymerization, a wet cake after dehydration, and a powder resin after drying may be used. It is desirable that the content is between 10 and 70% by weight. 10% by weight
If the amount is less than 70% by weight, the amount of wastewater will be too large compared to the amount of product, which is uneconomical. If it exceeds 70% by weight, the viscosity of the mixture of aqueous dispersion and organic liquid will increase significantly, making it difficult to operate. becomes difficult. Furthermore, if the average particle size of the coarse vinyl chloride resin exceeds 60 microns, it is undesirable because it causes streaks during thin film coating processing, roughening and matting of the surface of the molded product. Moreover, if it is less than 10 microns, the recovery efficiency of granular vinyl chloride resin and the recovery efficiency of the resin component from separated water will decrease. In addition, if the amount of coarse vinyl chloride resin added is less than 1% by weight, the recovery efficiency of the resin and the viscosity characteristics when made into a sol will be poor, while if it exceeds 70% by weight, the recovery efficiency of the resin will be improved and the separation will be poor. Although the ease of recovering the resin component from water is maintained, if the obtained product is made into plastisol and subjected to paste processing, the gelling property and mechanical strength of the molded product will be significantly reduced. The disadvantage is that the scope of use is limited. The organic liquid added to the aqueous dispersion of vinyl chloride resin is one that is sparingly soluble in water and does not dissolve or swell the resin during separation and recovery in the present invention. Generally, this organic liquid is
Those having a melting point of 20° C. or lower and a boiling point at normal pressure higher than the temperature during separation and recovery of the present invention, preferably 200° C. or higher are used. If an organic liquid having a boiling point lower than the temperature at the time of separation and recovery is used, additional equipment is required for recovery because the organic liquid evaporates, which is not economical. Of course, even if it does not meet the above-mentioned conditions as a single product, it may be used as a mixture as long as it satisfies the above-mentioned requirements. There are two reasons why organic liquids are required to be poorly soluble in water. Firstly, this is to reduce the amount entrained in the aqueous phase to be separated after mixing with the aqueous dispersion, thereby preventing loss of organic liquid and reducing wastewater treatment costs.Secondly, To aggregate resin particles dispersed in water via an organic liquid,
This is because the organic liquid needs to exist as a liquid phase with an interface between the resin particles and water.
Furthermore, if the organic liquid used is one that dissolves or swells the resin at the temperature during separation and recovery in the present invention, this is disadvantageous because the resin particles may be deformed or altered in quality. In addition, since most of the organic liquid used in the present invention remains in the product resin, it is necessary to avoid any liquid that would have an adverse effect on the operability and processability during paste processing and the quality of the molded product. In view of the above points, it is most natural and rational to use a liquid compounding agent commonly used in paste processing as an organic liquid. Examples of the organic liquid in the present invention include the following. (1) Phthalic acid alkyl ester plasticizers such as dioctyl phthalate, dinonyl phthalate, butyl lauryl phthalate, and methyl oleyl phthalate (2) Aromatic carboxylic acid ester plasticizers such as trioctyl trimellitate and diethylene glycol dibenzoate (3) ) Aliphatic dibasic acid ester plasticizers such as dioctyl adipate, dibutyl sebacate, and dioctyl tetrahydrophthalate (4) Phosphate ester plasticizers such as trioctyl phosphate and trichloroethyl phosphate (5) Diethylene glycol dicarbonate rate, 1.4
Fatty acid glycol ester plasticizers such as butylene glycol di-2-ethylhexanoate (6) Polyester plasticizers (7) Butyl oleate, methyl acetyl ricinolate 2,2,4-trimethyl-1,3-pentane Fatty acid esters such as diol diisoptylate, epoxidized soybean oil, epoxys such as octyl epoxystearate, chlorinated fatty acid methyl, chlorinated paraffins such as chlorinated paraffin, aliphatic dibasic acids such as dioctyl succinate Ester-based secondary plasticizers (8) Petroleum-based diluents such as mineral spirits and mineral turpentine, and long-chain alkylbenzene-based diluents such as dodecylbenzene (9) Liquid lubricants such as higher alcohols, liquid paraffin, and higher fatty acid alkyl esters Organic The amount of liquid added is 100% of the resin in the aqueous dispersion.
0.5 to 20 parts by weight, preferably 2 to 20 parts by weight
It should be selected within the range of 15 parts by weight. The amount added is
If it exceeds 20 parts by weight, the desired granules may not be obtained and a sol may be formed. Even if granules are obtained, the large content of organic liquid may make it difficult to remove water in the subsequent drying step. If the amount added is less than 0.5 parts by weight,
Very little of the desired granules are obtained. The mixing of the organic liquid and the aqueous dispersion of the resin is
It should be carried out at 70°C, preferably in the range 20-50°C. If the temperature exceeds 70°C, swelling and absorption of the resin by the organic liquid will be promoted, and coalescence will begin to occur due to softening of the resin, so there is a risk that the dispersibility of the final product will be significantly impaired. Any known method can be used to mix the organic liquid and the aqueous dispersion of the resin, but since the degree of mixing has a large effect on the aggregation efficiency of the resin with the organic liquid, it is preferable to mix the amount per unit volume of the mixing device. Mixed power is 1KW/ M3 (1 per cubic meter
kilowatts) and the product with the mixing time is
It should be 4KW・Hr/M 3 or more.
From the viewpoint of uniformity and continuity of mixing, it is preferable to use a high-speed rotating continuous mixer or a multi-blade continuous mixing tank as a mixing device, but ordinary stirring tank mixers and static top mixers are also recommended. Can be used. Next, in order to separate the aqueous phase from the assembled resin aggregate via the organic liquid, a known method may be used depending on the shape of the captured resin mixture. however,
The temperature must be in the range of 20-70°C to prevent softening and coalescence of the resin. The resin particles separated in the separation process are then sent to a drying process to remove the organic liquid and attached moisture. In this drying process, widely known drying equipment can be used, but it is necessary to set conditions such that the strength of resin aggregation and coalescence does not impair dispersibility during paste processing. In other words, the temperature of the resin to be dried during the drying process is 70°C or less, preferably 50°C.
Make it as follows. In this way, vinyl chloride resin can be obtained in high yield, and this resin has good fluidity and low scattering, and also has good viscosity characteristics when made into plastisol by conventional methods and thermal stability when made into molded products. It also has excellent physical properties. The method of the invention will now be explained by way of examples. Note that the average particle size of the vinyl chloride resin indicates the particle size at the 50% point in the weight distribution of the resin particles. In addition, the recovery efficiency of granular vinyl chloride resin was calculated using the following formula. Recovery efficiency = Weight of vinyl chloride resin sieved on a wire mesh with a predetermined opening/weight of vinyl chloride resin in the charged vinyl chloride latex x 100 (%) In addition, the sedimentation property and powder property of the resin , sol (resin 50g
and 30 g of di-2-ethylhexyl phthalate in a sieve machine) and the properties of the film will be explained below. Sedimentation property of resin in separated water after passing through a screen After collecting separated water in a glass container and allowing it to stand still,
A case where an almost transparent supernatant liquid is formed within 3 minutes is considered good, and a case where a supernatant liquid is not formed even after 10 minutes is judged poor. Angle of repose Indicates the ease of fluidity of powder; the smaller the value, the better the fluidity. Bulk specific gravity This is the apparent density of the powder, and the larger the value, the better the handling properties. Adhesion After placing the sample on paper and vibrating it horizontally, discard the sample and observe the amount of resin attached to the paper.
The less the better. Viscosity Burtskfield BM type viscometer rotor #4
Values at a sol temperature of 23°C when measured at 6 rpm (on the first day) and when left at 23°C for 7 days (after 7 days). North Finesse This indicates the particle size of the resin particles in the sol, and the larger the number, the finer it is (8 is the finest and 0 is the coarsest). Thermal stability The sol was poured into an aluminum mold and the 190
Changes in color tone after 30 minutes in a hot air atmosphere at ℃ are displayed in 5 levels from A (small change) to E (large change). Film strength The sol was coated on a 2 mm thick glass plate to a thickness of 400ÎŒ, heated to gel in a hot air atmosphere at 180°C for 10 minutes, and then formed into a film.JIS K-6301-
75 compliant No. 3 dumbbell, tensile speed 200mm/
Measure the tensile strength at break at min. Example 1 3000 g of an aqueous dispersion of vinyl chloride resin for paste processing (solid content 30% by weight, average particle size 1.2Ό),
400g of an aqueous dispersion (solid content 30% by weight) of coarse vinyl chloride resin having an average particle size of 45Ό and a
61g of 2-ethylhexyl phthalate was transferred into a container with an inner diameter of 10cm and an internal volume that had numerous stirring blades of 9cm in diameter inside.
Place in a 3.8 cylindrical stainless steel mixer,
After mixing at 1200 rpm for 10 minutes, an aqueous dispersion of a spherical resin composition was obtained. The spherical resin composition was separated from this dispersion using a 60-mesh wire mesh, and the material on the wire mesh was centrifugally dehydrated to obtain 826 g of wet granules. When this was dried in a hot air dryer at 35°C for 12 hours, 603 g of resin (A) was obtained. Example 2 3200 g of an aqueous dispersion of vinyl chloride resin for paste processing (solid content 30% by weight, average particle size 1.2Ό),
Coarse vinyl chloride resin powder with average particle size of 26Ό
300g and 100g of di-2-ethylhexyl phthalate
Example 1 except that g was mixed at 1000 rpm for 15 minutes.
The experiment was conducted using exactly the same equipment and procedure as in the previous study. The weight of the wet granules obtained was 1170 g, and the weight of the dry resin (B) was 831 g. Comparative Example 1 Using 3400 g of the aqueous dispersion of vinyl chloride resin for paste processing used in Example 1 (solid content 30% by weight) and 61 g of di-2-ethylhexyl phthalate, the same equipment and conditions as in Example 1 were carried out. The experiment was carried out according to the procedure. The weight of the wet granules obtained was 402 g;
The weight of the dry resin (C) was 285 g. Comparative Example 2 Using 2,600 g of the aqueous dispersion of vinyl chloride resin for paste processing used in Example 2 (however, the solid content was adjusted to 15% by weight), 800 g of coarse vinyl chloride resin powder, and 95 g of di-2-ethylhexyl phthalate. The experiment was conducted using exactly the same equipment, conditions, and procedures as in Example 2. The weight of the obtained wet weight is 1060g,
The weight of the dry resin (D) was 785 g. Comparative Example 3 3000 g of the aqueous dispersion of vinyl chloride resin for paste processing used in Example 1 (solid content 30% by weight),
500 g of an aqueous dispersion (solids content 32% by weight) of coarse vinyl chloride resin having an average particle size of 93Ό and a
An experiment was conducted using 64 g of 2-ethylhexyl phthalate using the same equipment, conditions, and procedure as in Example 1. The weight of the wet granules obtained was 866 g, and the weight of the dry resin (E) was 632 g. Reference Example 1 The aqueous dispersion of vinyl chloride resin for paste processing used in Example 1 was dried with a spray dryer at an inlet temperature of 160°C and an outlet temperature of 56°C, and pulverized with a tabletop pulverizer to obtain dry resin (F). I got it. The table shows the recovery efficiency and characteristics of resins (A) to (F). 【table】

Claims (1)

【特蚱請求の範囲】[Claims]  ペヌスト加工甚塩化ビニル暹脂の氎性分散液
に氎に難溶であ぀おか぀該塩化ビニル暹脂を溶解
又は膚最させない有機液䜓を添加しお混合するこ
ずにより、塩化ビニル暹脂を粒状集合䜓ずしお氎
盞より分離せしめた埌也燥するこずによ぀お、塩
化ビニル暹脂を回収するに際し、ペヌスト加工甚
塩化ビニル暹脂の氎性分散液に、平均粒埄が10〜
60ミクロンの塩化ビニル暹脂を、党暹脂量䞭〜
70重量ずなる範囲で添加するこずを特城ずする
ペヌスト加工甚塩化ビニル暹脂の回収方法。
1. By adding and mixing an organic liquid that is sparingly soluble in water and does not dissolve or swell the vinyl chloride resin into an aqueous dispersion of a vinyl chloride resin for paste processing, the vinyl chloride resin is formed into a granular aggregate in the aqueous phase. When recovering the vinyl chloride resin by separating it further and drying it, the aqueous dispersion of the vinyl chloride resin for paste processing has an average particle size of 10 to
60 micron vinyl chloride resin from 1 to 100% of the total resin amount
A method for recovering vinyl chloride resin for paste processing, characterized in that the amount is added within a range of 70% by weight.
JP22089882A 1982-12-16 1982-12-16 PEESUTOKAKOYOENKABINIRUJUSHINOKAISHUHOHO Expired - Lifetime JPH0248003B2 (en)

Priority Applications (1)

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JPH0248003B2 true JPH0248003B2 (en) 1990-10-23

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Country Link
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Publication number Priority date Publication date Assignee Title
US4914154A (en) * 1984-08-24 1990-04-03 Wacker-Chemie Gmbh Novel matting agent and its use

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