JPS6231015B2 - - Google Patents

Info

Publication number
JPS6231015B2
JPS6231015B2 JP55022830A JP2283080A JPS6231015B2 JP S6231015 B2 JPS6231015 B2 JP S6231015B2 JP 55022830 A JP55022830 A JP 55022830A JP 2283080 A JP2283080 A JP 2283080A JP S6231015 B2 JPS6231015 B2 JP S6231015B2
Authority
JP
Japan
Prior art keywords
acid
copolymer
diester
dispersion
unsaturated carboxylic
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
Application number
JP55022830A
Other languages
Japanese (ja)
Other versions
JPS56120780A (en
Inventor
Shoji Goto
Muneaki Tsurugatani
Yasuo Takenaka
Masanori Meguridate
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.)
TOKUSHU SEISHI KK
Original Assignee
TOKUSHU SEISHI KK
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 TOKUSHU SEISHI KK filed Critical TOKUSHU SEISHI KK
Priority to JP2283080A priority Critical patent/JPS56120780A/en
Publication of JPS56120780A publication Critical patent/JPS56120780A/en
Publication of JPS6231015B2 publication Critical patent/JPS6231015B2/ja
Granted legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/40—General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/41—Joining substantially flat articles ; Making flat seams in tubular or hollow articles
    • B29C66/45—Joining of substantially the whole surface of the articles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00—General aspects of processes or apparatus for joining preformed parts
    • B29C66/40—General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/41—Joining substantially flat articles ; Making flat seams in tubular or hollow articles

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

本発明は優れた䜎枩熱接着性ず耐ブロツキング
性ずのある被膜を䞎える氎性分散物及びそれで凊
理した䜎枩床においおも熱接着が可胜でしかも耐
ブロツキング性が良奜な感熱接着シヌトに関する
ものである。 䞀般に包装材料等ずしお広く䜿甚される玙、ア
ルミ箔、セロフアン等の熱接着が出来ない基材の
接着には各皮の感熱接着剀が䜿甚されるが、䞭で
も非公害化の点から特に熱可塑性暹脂の氎性分散
物が幅広く䜿甚されるようにな぀た。氎性分散物
を接着剀ずしお䜿甚する堎合の䞀般的な方法は、
基材に氎性分散物を塗工し、次いで也燥するこず
により基材䞊に熱ず圧力ずにより接着する性質を
有する被膜を圢成せしめお、基材ぞの熱接着性の
附䞎が行なわれる。 熱接着性を瀺す被膜が蚭けられた基材の接着
は、その䜿甚目的に応じお被膜面同志、あるいは
被膜面ず他基材面ずをあわせ熱ず圧力ずを加える
こずにより行なわれるが、この際、䜎い枩床で接
着可胜である皋省゚ネルギヌの点からも、曎には
シビアヌな接着加工枩床管理を必芁ずしない点か
らも奜たしい。曎にたた、工業的には基材の接着
は基材を䞀定速床で走行させながら行なわれるの
で、䜎い枩床でも熱接着できるこずは基材の高い
速床での走行䞋での熱接着を可胜にし、その結果
高生産性に぀ながる。 たた氎性分散物で凊理されお被膜が蚭けられた
基材は、そのたゝ熱接着されるこずは極めお少な
く、殆んどはそのたゝ䞀旊捲き取られるが、この
際被膜の粘着性が倧きいず、塗工被膜面ず基
材面やロヌル等の装眮ずの間でブロツキングが発
生し、取り扱いが極めお困難ずなり、捲き取り工
皋やその后の諞工皋印刷、充おん、接着等の
安定操䜜に支障をきたす。埓぀お、基材䞊の被膜
は䜎枩熱接着性以倖に良奜な耐ブロツキング性を
有しおいるこずが必芁である。 埓来より熱接着性を有する氎性系感熱接着剀ず
しお、ポリ酢酞ビニル系、ポリ塩化ビニル系、ポ
リ塩化ビニリデン系、ポリアクリル系等の熱可塑
性暹脂の氎性分散物が知られおいるが、これら公
知の氎性分散物の殆んどは䜎枩床で熱接着可胜な
ものはブロツキングし易く、逆に耐ブロツキング
性の良奜なものは熱接着可胜枩床が高枩床になる
ずいう性質を有しおおり、䞡方の性胜を満足する
被膜を䞎えない。この為、実甚性を考慮しお耐ブ
ロツキング性の良奜なものを遞び熱接着効率の方
を犠性にしおいるのが実情である。 改良法ずしお、䜎枩熱接着性のよい暹脂にワツ
クス゚マルゞペン、ポリ゚チレン゚マルゞペン、
セルロヌス、クレヌ、シリカ等の埮粉末等を耐ブ
ロツキング改良剀ずしお䜵甚するこずも行なわれ
るが、これらの方法では耐ブロツキング性は幟ら
か改良されるものの、反面䜎枩熱接着性が損なわ
れ満足すべき結果は埗られおいない。 たた、特開昭54―18689号報に斌いお、共重合
成分量を倚くし熱軟化枩床を䞋げた゚チレン系共
重合䜓にグリセリンの脂肪酞゚ステルを䜵甚した
氎性系感熱接着剀組成物が提案されおいるが、効
果を満足するには共重合成分量の高い範囲の暹脂
を䜿甚する必芁があるので暹脂自䜓の匷さが䜎
く、曎に耐ブロツキング性も悪くなるのでグリセ
リンの脂肪酞゚ステルは倚量添加しなければなら
なくなり、埓぀お接着が可胜ずなる枩床は䜎いも
のの接着匷床は䜎いずいう欠点がある。たた、被
膜の耐氎性、、耐熱性など他の実甚特性にも問題
がある。埓぀お、単に玙同志の接着剀ずしおは䜿
甚できるが、十分な接着匷床を必芁ずする甚途、
䟋えば内容物の充填を䌎なう包装分野等に斌いお
は䜿甚できず、極めお限定された特殊な甚途にし
か䜿甚できない。 たた最近、゚チレンずαβ―゚チレン系䞍飜
和カルボン酞よりなる共重合䜓で、そのカルボン
酞の䞀郚を金属むオンず䞭和せしめた熱可塑性暹
脂、謂ゆる゚チレン系アむオノマヌ暹脂は耐ブロ
ツキング性が良奜であるずいうこずで、その氎性
分散物が包装材料等の感熱接着剀ずしお䜿甚され
るようにな぀おきたが、このアむオノマヌヌ暹脂
はむオン結合を有する為に耐ブロツキング性は良
奜ずなる反面、熱流動性が乏しくなり、䜎枩熱接
着性に問題がある。 本発明者らは䜎い枩床䟋えば70―90℃で熱
接着が可胜でしかも耐ブロツキング性が良奜で䞔
぀十分高い接着匷床も有する氎性系接着剀に぀い
お鋭意研究を重ねた結果、共重合成分量の少ない
゚チレン系共重合䜓に特定の゚ステル化合物を䜵
甚すれば共存共重合䜓の有するすぐれた性質を損
なうこずなく䜎枩熱接着性が改良され、その氎性
分散物が前蚘芁求をすべお満足するこずを芋出し
本発明の完成に到぀た。 即ち本発明は、97〜85モルの゚チレンず〜
15モルのαβ―゚チレン系䞍飜和カルボン
酞、あるいは該䞍飜和カルボン酞の䞀郚がアルキ
ル゚ステルであるものずからなる゚チレン系共重
合䜓であ぀お、前蚘䞍飜和カルボン酞の少なくず
も10が䞭和されおいる共重合䜓ず、脂肪族二塩
基酞ゞ゚ステル及び又はスルホコハク酞ゞ゚ス
テルずを䞻成分ずする氎性分散物を提䟛するもの
である。曎に、かゝる氎性分散物で凊理したシヌ
トを提䟛するものである。 次に本発明を詳现に説明する。 本発明で甚いられる゚チレン系共重合䜓は97〜
85モル、奜たしくは95〜90モルの゚チレン
ず、〜15モル、奜たしくは〜10モルの
αβ―゚チレン系䞍飜和カルボン酞、堎合によ
りそのカルボン酞の䞀郚がアルキル゚ステルであ
るものずからなり、䞔぀αβ―䞍飜和カルボン
酞の少なくずも10が䞭和された゚チレン系共重
合䜓である。゚チレンの含有量が97モルを越え
るず安定な氎性分散物の補造が困難ずなり、たた
䜎枩熱接着性が適圓でなくなる。又逆に85モル
未満になるず接着匷床が䜎くなり、たた耐ブロツ
キング性が劣぀おくる。゚チレン系共重合䜓䞭の
アルキル゚ステルの含量は、該共重合䜓のカルボ
ン酞基の党量―COOXで衚わしたずき、―
COOはカルボン酞基であり、は、金属や
NH4等のアルカリむオン、及びアルキル基を瀺
す、の50以䞋ずするのが奜たしい。50を超
えるずきには安定な氎性分散物が埗難く、たた接
着匷床が䜎くなる。αβ―゚チレン系䞍飜和カ
ルボン酞の䟋ずしおは、アクリル酞、メタクリル
酞、マレむン酞、フマル酞、むタコン酞等があ
る。又αβ―゚チレン系䞍飜和カルボン酞アル
キル゚ステルの䟋ずしおは、䞊蚘カルボン酞のメ
チル、゚チル、ブチル等の゚ステルがある。゚チ
レンず共重合させるこれらの䞍飜和カルボン酞又
はそのアルキル゚ステルは単独でもたた二皮以䞊
䜵甚しおも䜿甚できる。又、接着胜、氎に察する
分散性、或いは耐ブロツキング性や熱接着性の補
助的なコントロヌル等を目的ずしお必芁に応じお
本発明の効果を損なわない範囲で、アクリル酞ヒ
ドロキシ゚チル、アクリルアミド、マレむン酞む
ミド等のαβ―゚チレン系䞍飜和カルボン酞誘
導䜓や、酢酞ビニル、ビニルアルコヌル、塩化ビ
ニル、スチレン等のビニル系単量䜓等を含有させ
た共重合䜓も䜿甚するこずができる。 尚、該共重合䜓䞭のカルボン酞基の党量の少な
くずも10が䞭和されおいる。䞭和量が10未満
では氎分散化が困難ずなる。最適䞭和量は䞭和物
の皮類や共重合成分量により異なり䞀抂に決める
こずはできないが、共重合成分量が少ない堎合に
は䞭和量を高く、逆に倚い堎合には䞭和量は䜎く
するのが安定な氎性分散物を埗る䞊で奜たしく、
実隓的に容易に決めるこずができる。 䞭和成分はカルボン酞を䞭和できるもので䞔぀
氎分散物の安定化を阻害しないものであればどん
なものでもよいが、実甚性からナトリりム、カリ
りム等のアルカリ金属やアンモニりムが奜たし
い。尚、本発明䞭で蚀う䞭和床は分散物ずしお存
圚しおいる時の共重合䜓䞭のカルボン酞の䞭和量
を瀺す。埓぀お、アンモニりム䞭和のように塗工
后の也燥脱氎で揮発し易いものでの䞭和のず
きには、塗膜に斌ける暹脂の䞭和量は分散物䞭の
それに范べお䜎くなり、也燥条件によ぀おは䞭和
量が零ずなる堎合もある。 䞭和の時期は暹脂のずきに行な぀おもよく、た
た氎分散物を補造するずきに行な぀おもよい。ア
ンモニりム䞭和の堎合には、揮発性や臭気の点か
ら氎分散物を補造する際に行なうのが奜たしい。 かゝる共重合䜓は単独で或いは耐ブロツキング
性や䜎枩接着性のコントロヌル等を目的ずしお二
皮以䞊混合䜿甚するこずもできる。 以䞊の劂き゚チレン系共重合䜓は、゚チレン
αβ―゚チレン系䞍飜和カルボン酞゚ステル共
重合䜓を出発原料ずする堎合には䟋えば特公昭49
―31556号公報、゚チレンαβ―゚チレン系
䞍飜和カルボン酞共重合䜓を出発原料ずする堎合
には䟋えば特公昭39―6810号公報等公知の方法で
容易に埗られる。 本発明に斌いお甚いる脂肪族二塩基酞ゞ゚ステ
ルは、脂肪族二塩基酞ず䟡アルコヌルずから埗
られるゞ゚ステル、及び脂肪族二塩基酞ず䟡ア
ルコヌルずモノカルボン酞ずから埗られるポリ゚
ステル系二塩基酞ゞ゚ステルである。脂肪族二塩
基酞ずしおは、HOOC――COOHなる䞀般匏
に斌いおがCHCH、CH2o、䜆しは〜
10の敎数である二塩基酞である。䟋えば、コハク
酞、アゞピン酞、アれラむン酞、セバシン酞等を
䟋瀺するこずができる。アルコヌルずしおは、゚
タノヌル、ブタノヌル、オクタノヌル、デカノヌ
ル、゚チレングリコヌル、プロピレングリコヌル
等の炭玠数が〜15の䟡及び䟡アルコヌルで
ある。モノカルボン酞ずしおはラりリン酞、パル
ミチン酞、ステアリン酞等の炭玠数が12〜18の脂
肪酞である。 具䜓的に脂肪族二塩基酞ゞ゚ステルの䟋ずし
お、マレむン酞ゞブチル、マレむン酞ゞオクチル
等のマレむン酞のゞ゚ステル、フマル酞ゞブチ
ル、フマル酞ゞオクチル等のフマル酞のゞ゚ステ
ルコハク酞ゞヘキシル、コハク酞ゞオクチル等
のコハク酞のゞ゚ステルアゞピン酞ゞ゚チル、
アゞピン酞ゞブチル、アゞピン酞ゞオクチル、ア
ゞピン酞ゞむ゜デシル、アゞピン酞オクチル―デ
シル、アゞピン酞ゞデシル、ポリプロピレンアゞ
ペヌト、ポリ゚ステル系アゞペヌト等のアゞピン
酞のゞ゚ステルアれラむン酞ゞブチル、アれラ
むン酞ゞオクチル等のアれラむン酞のゞ゚ステ
ルセバシン酞ゞブチル、セバシン酞ゞヘキシ
ル、セバシン酞ゞオクチル、セバシン酞オクチル
―デシル、ポリ゚チレンセバケヌト、ポリプロピ
レンセバケヌト、ポリ゚ステル系セバケヌト等の
セバシン酞のゞ゚ステルを䟋瀺するこずができ
る。かゝる化合物はポリ塩化ビニル等の可塑剀ず
しお䜿甚されおおり容易に入手するこずができ
る。 これらの脂肪族二塩基酞ゞ゚ステルは単独或い
は二皮以䞊を混合しお䜿甚するこずができる。こ
れらのゞ゚ステルは共存する暹脂の皮類や添加量
を適圓に遞択すれば党お効果を発揮するが、その
奜適条件は実隓により容易に求められる。これら
のゞ゚ステルの䞭で、工業的芏暡での生産が行な
われおいる点、又性胜を満足する察象暹脂範囲が
比范的広い点等から特にアゞピン酞のゞ゚ステル
やセバシン酞のゞ゚ステルが奜たしい。又、塗工
后の也燥枩床が高い、又塗工后熱接着たでの時間
が長い等のゞ゚ステルの揮散を促進するような甚
途に本発明の氎性分散物を䜿甚する堎合には、沞
点が200℃以䞊のゞ゚ステルを遞択するのが望た
しい。 本発明に斌いお甚いるスルホコハク酞ゞ゚ステ
ルは、次ぎの䞀般匏
The present invention relates to an aqueous dispersion that provides a film with excellent low-temperature thermal adhesion and blocking resistance, and a heat-sensitive adhesive sheet treated with the dispersion that can be thermally bonded even at low temperatures and has good blocking resistance. Various heat-sensitive adhesives are used to bond substrates that cannot be thermally bonded, such as paper, aluminum foil, and cellophane, which are widely used as packaging materials. Among them, thermoplastic resins are especially used from the viewpoint of non-pollution. Aqueous dispersions of are now widely used. A common method for using aqueous dispersions as adhesives is to
The aqueous dispersion is applied to the substrate and then dried to form a film on the substrate that has the property of adhering to the substrate by heat and pressure, thereby imparting thermal adhesive properties to the substrate. Adhesion of base materials coated with a film exhibiting thermal adhesive properties is carried out by applying heat and pressure to the coated surfaces or to the surface of another base material, depending on the purpose of use. In fact, it is preferable to be able to bond at a low temperature, both from the point of view of energy saving and also from the point of not requiring severe temperature control during the bonding process. Furthermore, industrially, bonding of substrates is carried out while the substrates are running at a constant speed, so being able to thermally bond them even at low temperatures makes it possible to thermally bond them while the substrates are running at high speeds. This results in high productivity. Furthermore, substrates treated with an aqueous dispersion and coated with a film are rarely thermally bonded as is, and in most cases they are simply peeled off, but in this case the film is highly adhesive. Blocking occurs between the coated (coating) surface and the substrate surface or equipment such as rolls, making it extremely difficult to handle and causing problems during the rolling process and subsequent processes (printing, filling, adhesion, etc.). This will impede stable operation. Therefore, the coating on the substrate must have good blocking resistance in addition to low-temperature thermal adhesion. Conventionally, aqueous dispersions of thermoplastic resins such as polyvinyl acetate, polyvinyl chloride, polyvinylidene chloride, and polyacrylic resins have been known as aqueous heat-sensitive adhesives with thermal adhesive properties. Most aqueous dispersions have the property that those that can be thermally bonded at low temperatures are easily blocked, and conversely, those that have good blocking resistance have a high temperature that allows thermal bonding. does not provide a coating that satisfies the performance of For this reason, the reality is that in consideration of practicality, a material with good blocking resistance is selected at the expense of thermal adhesion efficiency. As an improved method, wax emulsion, polyethylene emulsion,
Fine powders of cellulose, clay, silica, etc. are also used together as anti-blocking agents, but although these methods improve anti-blocking properties to some extent, they impair low-temperature thermal adhesion properties and are unsatisfactory. No results have been obtained. Furthermore, in JP-A-54-18689, an aqueous heat-sensitive adhesive composition was proposed in which a fatty acid ester of glycerin was used in combination with an ethylene copolymer with a high copolymerization content and a low heat softening temperature. However, in order to achieve the desired effect, it is necessary to use a resin with a high copolymerization content, which results in low strength of the resin itself and poor blocking resistance, so a large amount of fatty acid ester of glycerin should not be added. Therefore, although the temperature at which bonding is possible is low, the bonding strength is low. There are also problems with other practical properties of the coating, such as water resistance and heat resistance. Therefore, although it can be used simply as an adhesive between papers, it can also be used for applications that require sufficient adhesive strength.
For example, it cannot be used in the field of packaging that involves filling the contents, and can only be used for very limited special purposes. Recently, thermoplastic resins made of copolymers of ethylene and α,β-ethylenically unsaturated carboxylic acids, with some of the carboxylic acids neutralized with metal ions, so-called ethylene-based ionomer resins, have been developed to have anti-blocking properties. Because of its good properties, its aqueous dispersion has come to be used as a heat-sensitive adhesive for packaging materials, etc. However, since this ionomer resin has ionic bonds, it has good blocking resistance. Thermal fluidity becomes poor and there are problems with low-temperature thermal adhesion. The present inventors have conducted intensive research on water-based adhesives that can be thermally bonded at low temperatures (e.g. 70-90℃), have good blocking resistance, and have sufficiently high adhesive strength. If a specific ester compound is used in combination with an ethylene-based copolymer having a small amount of ethylene, the low-temperature thermal adhesion will be improved without impairing the excellent properties of the copolymer, and the aqueous dispersion will satisfy all of the above requirements. Heading: The present invention has been completed. That is, the present invention provides 97 to 85 mol% ethylene and 3 to 85 mol% ethylene.
An ethylene copolymer comprising 15 mol% of an α,β-ethylenically unsaturated carboxylic acid, or a part of the unsaturated carboxylic acid is an alkyl ester, the copolymer comprising at least 10% of the unsaturated carboxylic acid. The present invention provides an aqueous dispersion containing as main components a copolymer with a neutralized percentage and an aliphatic dibasic acid diester and/or a sulfosuccinic acid diester. Furthermore, a sheet treated with such an aqueous dispersion is provided. Next, the present invention will be explained in detail. The ethylene copolymer used in the present invention is 97~
85 mol %, preferably 95-90 mol % ethylene and 3-15 mol %, preferably 5-10 mol % α,β-ethylenically unsaturated carboxylic acid, optionally in which some of the carboxylic acids are alkyl It is an ethylene copolymer consisting of an ester and at least 10% of the α,β-unsaturated carboxylic acid is neutralized. If the ethylene content exceeds 97 mol %, it becomes difficult to produce a stable aqueous dispersion, and the low-temperature thermal adhesiveness becomes inadequate. On the other hand, 85 mol%
If it is less than that, the adhesive strength will be low and the blocking resistance will be poor. The content of alkyl ester in the ethylene copolymer is determined by the total amount of carboxylic acid groups in the copolymer (when expressed as R-COOX, R-
COO is a carboxylic acid group, X is H, metal or
It is preferable that the amount of NH 4 and other alkali ions, and (representing an alkyl group) is 50% or less. When it exceeds 50%, it is difficult to obtain a stable aqueous dispersion and the adhesive strength becomes low. Examples of α,β-ethylenically unsaturated carboxylic acids include acrylic acid, methacrylic acid, maleic acid, fumaric acid, and itaconic acid. Examples of α,β-ethylenically unsaturated carboxylic acid alkyl esters include esters of the above-mentioned carboxylic acids such as methyl, ethyl, and butyl. These unsaturated carboxylic acids or alkyl esters thereof to be copolymerized with ethylene can be used alone or in combination of two or more. In addition, hydroxyethyl acrylate, acrylamide, maleic acid, etc. may be added as necessary for the purpose of adhesion, water dispersibility, blocking resistance, thermal adhesion, etc., to the extent that does not impair the effects of the present invention. Copolymers containing α,β-ethylenically unsaturated carboxylic acid derivatives such as imides, vinyl monomers such as vinyl acetate, vinyl alcohol, vinyl chloride, and styrene can also be used. Note that at least 10% of the total amount of carboxylic acid groups in the copolymer is neutralized. If the amount of neutralization is less than 10%, water dispersion becomes difficult. The optimal amount of neutralization varies depending on the type of neutralized substance and the amount of copolymerized components, and cannot be determined unconditionally, but if the amount of copolymerized components is small, the amount of neutralization should be increased, and conversely, if the amount of copolymerized components is large, the amount of neutralization should be In order to obtain a stable aqueous dispersion, it is preferable to lower the
It can be easily determined experimentally. Any neutralizing component may be used as long as it can neutralize the carboxylic acid and does not inhibit the stabilization of the aqueous dispersion, but from the viewpoint of practicality, alkali metals such as sodium and potassium and ammonium are preferred. Note that the degree of neutralization referred to in the present invention indicates the amount of neutralization of carboxylic acid in the copolymer when it exists as a dispersion. Therefore, when neutralizing with something that easily volatizes during drying (dehydration) after coating, such as ammonium neutralization, the amount of neutralized resin in the coating film is lower than that in the dispersion. Depending on the drying conditions, the amount of neutralization may be zero. Neutralization may be carried out at the time of preparing the resin, or may be carried out at the time of producing the aqueous dispersion. In the case of ammonium neutralization, it is preferably carried out when producing an aqueous dispersion from the viewpoint of volatility and odor. Such copolymers may be used alone or in combination of two or more for the purpose of controlling blocking resistance and low temperature adhesion. The above ethylene copolymers are ethylene/
When α,β-ethylenically unsaturated carboxylic acid ester copolymer is used as a starting material, for example,
When an ethylene/α,β-ethylenically unsaturated carboxylic acid copolymer is used as a starting material, it can be easily obtained by a known method such as in Japanese Patent Publication No. 39-6810. The aliphatic dibasic acid diesters used in the present invention include diesters obtained from an aliphatic dibasic acid and a monohydric alcohol, and polyester diesters obtained from an aliphatic dibasic acid, a dihydric alcohol, and a monocarboxylic acid. It is a basic acid diester. As an aliphatic dibasic acid, in the general formula HOOC-R-COOH, R is CH=CH, (CH 2 ) o , where n is 2 to
It is a dibasic acid that is an integer of 10. Examples include succinic acid, adipic acid, azelaic acid, and sebacic acid. Examples of the alcohol include monohydric and dihydric alcohols having 1 to 15 carbon atoms, such as ethanol, butanol, octanol, decanol, ethylene glycol, and propylene glycol. Monocarboxylic acids include fatty acids having 12 to 18 carbon atoms, such as lauric acid, palmitic acid, and stearic acid. Specific examples of aliphatic dibasic acid diesters include diesters of maleic acid such as dibutyl maleate and dioctyl maleate; diesters of fumaric acid such as dibutyl fumarate and dioctyl fumarate; dihexyl succinate, dioctyl succinate, etc. Diester of succinic acid; diethyl adipate,
Diesters of adipic acid such as dibutyl adipate, dioctyl adipate, diisodecyl adipate, octyl-decyl adipate, didecyl adipate, polypropylene adipate, polyester adipate; diesters of azelaic acid such as dibutyl azelaate and dioctyl azelate; sebacin Examples include diesters of sebacic acid such as dibutyl sebacate, dihexyl sebacate, dioctyl sebacate, octyl-decyl sebacate, polyethylene sebacate, polypropylene sebacate, and polyester sebacate. Such compounds are used as plasticizers for polyvinyl chloride and the like and are easily available. These aliphatic dibasic acid diesters can be used alone or in combination of two or more. All of these diesters exhibit their effects if the type and amount of coexisting resins are appropriately selected, but the preferred conditions can be easily determined through experiments. Among these diesters, diesters of adipic acid and diesters of sebacic acid are particularly preferred because they are produced on an industrial scale and the range of target resins that satisfy the performance is relatively wide. In addition, when the aqueous dispersion of the present invention is used in applications where the drying temperature after coating is high, or the time required for thermal adhesion after coating is long, and the volatilization of the diester is promoted, the boiling point is 200%. It is desirable to select a diester with a temperature above ℃. The sulfosuccinic acid diester used in the present invention has the following general formula:

【匏】で瀺すものであ る。匏䞭で、R1R2は炭玠数〜20のアルキル
基であり、同䞀でも又盞異な぀おいおもよい。
はNa、等のアルカリ金属、たたNH4を瀺す。
かゝる化合物はマレむン酞ずアルコヌルずスルホ
ン化剀ずの反応により容易に埗られ、マレむン酞
の゚ステル化成分がグリコヌルやヒドロキシアミ
ンより誘導されるゞ゚ステルタむプも効果がみら
れるが、氎性分散物の安定性、入手の容易性の点
等から䟡のアルコヌルより誘導されるゞ゚ステ
ルタむプが奜たしい。具䜓的には、゜ゞりムスル
ホゞメチルサクシネヌト、゜ゞりムスルホゞブチ
ルサクシネヌト、゜ゞりムスルホゞオクチルサク
シネヌト、゜ゞりムスルホゞトリデシルサクシネ
ヌトト等を䟋瀺するこずができる。これらの化合
物は単独で、或いは必芁な堎合には二皮以䞊混合
しお䜿甚しおもよい。尚、これらの化合物は幟ら
かのモノ゚ステルや未反応物を含有しおいる堎合
もあるが、これらモノ゚ステルや未反応物は氎性
分散物の安定化の阻害や泡立ちの原因になり易い
ので極力少なくするのが奜たしい。たた、これら
の化合物は䞀般にメタノヌル、゚タノヌル、プロ
ピレングリコヌル、ブチルカルビトヌル等の溶剀
を含有した氎溶液ずしお垂販されおおり界面掻性
剀ずしお広く䜿甚されおいるが、本発明の効果は
含有されおいる溶剀の皮類に巊右されないので、
溶剀を含んだたゝで䜿甚できるが、必芁ならば溶
剀を陀去しお䜿甚するこずもできる。 本発明の氎性分散物の調補は、脂肪族二塩基酞
ゞ゚ステル及び又はスルホコハク酞ゞ゚ステル
を溶融状態で、又溶液状態で混合しお共重合䜓䞭
に予じめ配合せしめおおき、この共重合䜓を氎䞭
に乳化分散させる方法、或いは共重合䜓及びこれ
らのゞ゚ステルを氎䞭に䞀緒に乳化分散させる方
法によ぀おも可胜であるが、混合時の副反応や乳
化分散時の配合ゞ゚ステルの加氎分解反応を䌎な
い易いのでさけるのが奜たしく、䞀般には予じめ
共重合䜓を氎䞭に乳化分散せしめ、次いでこの共
重合䜓分散液䞭に䞊蚘ゞ゚ステル化合物を配合す
るのがよい。 共重合䜓の分散液は共重合䜓の䞀皮又は二皮以
䞊をそのたゝ或いは䞭和の為のアルカリ存圚䞋
に、必芁に応じお機械的安定性、塗工時の基材ず
の濡れをよくする目的で少量の公知の陰むオン又
は非むオン性界面掻性剀を添加しお、氎䞭に溶解
又は乳化分散させるこずで容易に埗られる。分散
液䞭の共重合䜓の固圢分量は䞀般には20〜60重量
である。 䞀方、脂肪族二塩基酞ゞ゚ステル、スルホコハ
ク酞ゞ゚ステルはそのたゝで或いは氎䞭に少量の
乳化分散剀の存圚䞋に又は非存圚䞋に乳化分散さ
せお前蚘共重合䜓の分散液䞭に配合する。 本発明の目的を達成する為に氎性分散物䞭に配
合するゞ゚ステル化合物の量は、配合するゞ゚ス
テル化合物の皮類や共重合䜓の組成により若干異
なるが、分散物䞭の共重合䜓100重量郚に察しお
少なくずも玔分ずしお重量郚あれば効果がみら
れる。配合量の増倧ず共に性胜も向䞊するが、あ
る量以䞊になるず逆に接着性胜の䜎䞋や分散物の
安定性の䜎䞋をきたす。その䞊限配合量は脂肪族
二塩基酞ゞ゚ステル又はスルホコハク酞ゞ゚ステ
ルのいづれか䞀方の配合の堎合に斌いおは、玄10
重量郚であり、䜵甚配合の堎合には高配合量たで
性胜の向䞊がみられ玄20重量郚である。尚、䜵甚
䜿甚の堎合、経枈性や安定性の点から重量比で脂
肪族二塩基酞ゞ゚ステルスルホコハク酞ゞ゚ス
テルが〜の範囲で䜿甚するのが奜た
しい。接着性改良床合、経枈性を考慮すれば、こ
れらゞ゚ステル化合物の配合量は〜15重量郚の
範囲が奜たしい。尚、䞀般には同䞀配合量で比范
した堎合、脂肪族二塩基酞ゞ゚ステルずスルコハ
ク酞ゞ゚ステルのいづれか䞀方を䜿甚したものよ
り䜵甚したものの方が䜎枩熱接着性は良奜ずな
り、たずえば単独䜿甚に比べ接着可胜最䜎枩床が
玄℃、堎合によ぀おは玄10℃䞋がる。 本発明で埗られる氎性分散物は前蚘共重合䜓ず
脂肪族二塩基酞ゞ゚ステル及び又はスルホコハ
ク酞ゞ゚ステルずを䞻成分ずしお含有するこずを
特城ずするものであるが、通垞氎性分散物に添加
される公知の添加剀、䟋えば界面掻性剀、可塑
剀、防ふ剀、消泡剀、増粘剀、垯電防止剀、耐ブ
ロツキング剀、滑り剀、玫倖線吞収剀等は勿論の
こず、コストダりン、塗工性の調敎等を目的ずし
お又はブロツキング性や接着性の補助的なコント
ロヌル等を目的ずしお、必芁に応じお本発明の氎
性分散物ず盞溶性のあるポリ酢酞ビニル、ポリ塩
化ビニル、ポリ塩化ビニリデン、ポリ゚チレン―
酢酞ビニル、ポリアクリル等の公知の氎性分散
物、たた也燥促進を目的ずしお゚タノヌル、む゜
プロピルアルコヌル等の有機溶剀等を本発明の目
的ずする特性が阻害されない範囲で配合するこず
ができる。 本発明の氎性分散物は、䞊質玙、合成玙等の
玙、アルミ箔等の合属箔、セロフアン、䞍織垃、
ポリオレフむン等のプラスチツクシヌト、さらに
これら基材の耇合基材䞊に耐ブロツキング性に優
れ、䞔぀䜎枩での熱接着が可胜で、䞔぀接着した
堎合高い接着匷床を有する被膜を提䟛するのに有
甚である。基材䞊に被膜を圢成させる方法は、䞀
般の玙コヌテむング等に斌いお䜿われおいる既存
の塗垃方匏、䟋えばバヌコヌタヌ、゚アヌナむフ
コヌタヌ、ロヌルコヌタヌ等で氎性分散物を基材
に塗垃し、さらに通垞の也燥工皋を通しお氎分を
蒞発させるこずによりできる。塗垃量は基材の平
滑性、浞透性等によ぀お異なるが、固圢分量で
2gm2以䞊塗垃すれば本発明の目的ずする䜎枩
床においお熱接着が可胜でしかも耐ブロツキング
性が良奜な感熱接着シヌトを埗るこずができる。 かゝる本発明の氎性分散物で凊理したシヌト
は、䜎い枩床でも熱接着が可胜であり、しかも接
着した堎合十分高い接着匷床を瀺し、さらに耐ブ
ロツキング性に優れた被膜を有しおいる為、取り
扱いが容易であり、塗垃から接着たでの工皋䞊の
トラブルもなくシビアヌな接着過床管理を必芁ず
せずに高速床走行䞋に安定しお熱接着でき、高い
生産性䞋に高品質の補品を安定しお補造するこず
ができる。熱接着を必芁ずする甚途の殆んどに斌
いお、本発明の䜎い枩床で熱接着でき䞔぀耐ブロ
ツキング性の良奜な感熱接着シヌトは有甚であ
り、䟋瀺すれば菓子補品や食品、化孊補品、家庭
日甚品、化粧品等の各皮内容物の包装材料ずし
お、たた接着剀を裏面に塗垃したシヌトの衚に電
算機のラむンプリンタヌ等で宛先きや内容をプリ
ントし、しかる后぀折りし熱圧着させお枚の
ハガキにする甚途等で有甚である。以䞋実斜䟋で
本発明の内容を具䜓的に説明するが、これら実斜
䟋により本発明が限定されるものではない。 尚、実斜䟋䞭で瀺す特性の評䟡は特蚘ない限り
以䞋の方法で行な぀た。各分散物を䞊質玙
75gm2又はアルミ箔17Όにバヌコヌタ
ヌで塗垃しおこれを100℃で分間也燥しお感熱
接着シヌトを埗た。熱接着は埗られた感熱接着シ
ヌトの分散物塗垃面同志を合わせおこれにセンチ
ネルヒヌトシヌラヌにより荷重Kgcm2を秒間
かけお各枩床に斌いお行な぀た。接着性の評䟡方
法は、この接着シヌトから詊隓片を切りずり、こ
れを匕匵り詊隓機で匕匵り速床200mm分で接着
面に察しお90゜の方向に匕匵り剥離の際の匷床
15mmを求める事で行な぀た。又、他の接
着性評䟡基準ずしお䞊質玙に塗工したサンプルの
堎合に斌いお、剥離の際の玙局の砎壊皋床を求め
る事で行な぀た。その評䟡は次の基準に埓぀お行
な぀た。 〇剥離に際しおほが党面が玙局砎壊する、 △剥離に際しお郚分的に玙局砎壊する、 ×剥離に際しお玙局砎壊党くなし。 耐ブロツキング性の評䟡は、玄5gm2固圢
分塗垃したアルミ箔17Όの塗垃面同志又は
塗垃面ず非塗垃面ずを合せおこれに0.5Kgcm2の
荷重をかけお30℃、湿床60の恒枩恒湿床䞋に攟
眮し、24時間后に手で剥離しおブロツキングの床
合を評䟡した。耐ブロツキング性の評䟡は次の基
準に埓぀お行な぀た。 〇粘着性殆んどなし △若干粘着性あり ×かなり粘着性あり 実斜䟋  含有量92モルの゚チレンずモルのメタク
リル酞より成り、そのメタクリル酞の29がナト
リりムむオンによ぀お䞭和されおいる共重合䜓の
氎性分散液固圢分濃床40重量、粘床
130cps、オレむン酞゜ヌダ量固圢分重量に察し
0.5含有に、衚に瀺すようなゞ゚ステ化合
物を共重合䜓の重量100郚に察しお郚添加し
た。埗られた氎性分散物をアルミ箔に6gm2
固圢分塗垃し、この感熱接着シヌトの䜎枩で
の熱接着性及び耐ブロツキング性を枬定した。比
范の為にゞ゚ステル化合物の配合されおいない分
散液で凊理したシヌトも枬定した。その結果は衚
に瀺すずおりである。衚から明らかな劂く、本
発明の分散物で凊理した接着シヌトは、75℃でも
熱接着可胜であり、比范䟋にくらべ著しく䜎枩接
着性が改良されおおり、しかも耐ブロツキング性
も良奜である。たた、脂肪族二塩基ゞ゚ステルず
スルホコハク酞ゞ゚ステルずを䜵甚するずさらに
䜎枩熱着性が改良されるこずが刀る。
It is shown by [Formula]. In the formula, R 1 and R 2 are alkyl groups having 1 to 20 carbon atoms, and may be the same or different. X
represents an alkali metal such as Na or K, or NH 4 .
Such compounds can be easily obtained by the reaction of maleic acid, alcohol, and a sulfonating agent, and a diester type in which the esterified component of maleic acid is derived from glycol or hydroxyamine is also effective; A diester type derived from a monohydric alcohol is preferred from the viewpoint of stability and availability. Specific examples include sodium sulfodimethyl succinate, sodium sulfodibutyl succinate, sodium sulfodioctylsuccinate, and sodium sulfoditridecyl succinate. These compounds may be used alone or in combination of two or more if necessary. Note that these compounds may contain some monoesters and unreacted substances, but these monoesters and unreacted substances tend to hinder the stabilization of the aqueous dispersion and cause foaming, so avoid using them as much as possible. It is preferable to reduce the amount. In addition, these compounds are generally commercially available as aqueous solutions containing solvents such as methanol, ethanol, propylene glycol, butyl carbitol, etc., and are widely used as surfactants. Because it does not depend on the type of
It can be used with the solvent still in it, but it can also be used after removing the solvent if necessary. The aqueous dispersion of the present invention is prepared by mixing an aliphatic dibasic acid diester and/or a sulfosuccinic acid diester in a molten state or a solution state and blending the copolymer in advance. This is possible by emulsifying and dispersing the copolymer in water, or by emulsifying and dispersing the copolymer and these diesters together in water, but side reactions during mixing and hydrolysis of the blended diesters during emulsification and dispersion are possible. It is preferable to avoid this because it tends to cause a reaction. Generally, it is preferable to emulsify and disperse the copolymer in water in advance, and then blend the above-mentioned diester compound into the copolymer dispersion. The copolymer dispersion can be prepared by adding one or more of the copolymers as is or in the presence of an alkali for neutralization, as necessary to improve mechanical stability and wettability with the substrate during coating. It can be easily obtained by adding a small amount of a known anionic or nonionic surfactant for the purpose of improving the composition and dissolving or emulsifying it in water. The solids content of the copolymer in the dispersion is generally 20 to 60% by weight. On the other hand, aliphatic dibasic acid diesters and sulfosuccinic acid diesters are incorporated into the copolymer dispersion as they are or by emulsifying and dispersing them in water in the presence or absence of a small amount of an emulsifying dispersant. The amount of diester compound to be blended into the aqueous dispersion in order to achieve the purpose of the present invention varies slightly depending on the type of diester compound to be blended and the composition of the copolymer; On the other hand, if the pure content is at least 1 part by weight, the effect can be seen. Performance improves as the amount added increases, but when the amount exceeds a certain level, adhesive performance and stability of the dispersion deteriorate. The upper limit of the blending amount is approximately 10% when either aliphatic dibasic acid diester or sulfosuccinic acid diester is blended.
It is about 20 parts by weight, and when used in combination, performance is improved even when the amount is increased. In addition, when used in combination, it is preferable to use the aliphatic dibasic acid diester:sulfosuccinic acid diester in a weight ratio of 1:1 to 5:1 from the viewpoint of economy and stability. Considering the degree of improvement in adhesion and economic efficiency, the amount of these diester compounds blended is preferably in the range of 2 to 15 parts by weight. Generally speaking, when comparing the same blending amounts, the combination of aliphatic dibasic acid diester and sulfuccinic acid diester has better low-temperature thermal adhesion properties than the combination of either diester and sulfuccinic acid diester, and for example, adhesiveness is better than when using them alone. The minimum temperature will drop by about 5°C, and in some cases by about 10°C. The aqueous dispersion obtained in the present invention is characterized by containing the above-mentioned copolymer and an aliphatic dibasic acid diester and/or a sulfosuccinic acid diester as main components. Not only well-known additives such as surfactants, plasticizers, defoaming agents, antifoaming agents, thickeners, antistatic agents, anti-blocking agents, slip agents, and ultraviolet absorbers, but also for reducing costs and coatings. Polyvinyl acetate, polyvinyl chloride, polyvinylidene chloride, which are compatible with the aqueous dispersion of the present invention, may be added as necessary for the purpose of adjusting workability or for supplementary control of blocking properties and adhesion. ,polyethylene-
Known aqueous dispersions such as vinyl acetate and polyacrylic, as well as organic solvents such as ethanol and isopropyl alcohol for the purpose of accelerating drying, may be blended within a range that does not impede the properties aimed at by the present invention. The aqueous dispersion of the present invention can be applied to papers such as high-quality paper and synthetic paper, composite foils such as aluminum foil, cellophane, nonwoven fabrics,
It is useful for providing coatings on plastic sheets such as polyolefin and composite substrates of these substrates that have excellent blocking resistance, can be thermally bonded at low temperatures, and have high adhesive strength when bonded. . The method for forming a film on the substrate is to apply an aqueous dispersion to the substrate using an existing coating method used in general paper coating, such as a bar coater, air knife coater, roll coater, etc. Further, water can be evaporated through a conventional drying process. The amount of application varies depending on the smoothness and permeability of the base material, but it depends on the solid content.
If it is coated in an amount of 2 g/m 2 or more, it is possible to obtain a heat-sensitive adhesive sheet that can be thermally bonded at low temperatures, which is the object of the present invention, and has good blocking resistance. The sheet treated with the aqueous dispersion of the present invention can be thermally bonded even at low temperatures, and when bonded, exhibits sufficiently high adhesive strength, and has a coating with excellent blocking resistance. It is easy to handle, there are no problems in the process from coating to adhesion, and it can be thermally bonded stably under high-speed running without the need for severe excessive adhesion control, producing high-quality products with high productivity. It can be manufactured stably. The heat-sensitive adhesive sheet of the present invention, which can be thermally bonded at low temperatures and has good blocking resistance, is useful in most applications that require thermal bonding; examples include confectionery products, foods, chemical products, It can be used as a packaging material for various contents such as household daily necessities and cosmetics, and can be used by printing the address and contents on the front side of the sheet with adhesive applied to the back side using a computer line printer, etc., then folding it in half and bonding it under heat. It is useful for making a single postcard, etc. EXAMPLES The content of the present invention will be specifically explained below with reference to Examples, but the present invention is not limited to these Examples. In addition, the evaluation of the characteristics shown in the examples was performed by the following method unless otherwise specified. Each dispersion was coated on high-quality paper (75 g/m 2 ) or aluminum foil (17 ÎŒm) using a bar coater and dried at 100° C. for 1 minute to obtain a heat-sensitive adhesive sheet. Thermal bonding was carried out at various temperatures by applying a load of 1 kg/cm 2 for 1 second to the dispersion-coated surfaces of the heat-sensitive adhesive sheets obtained using a sentinel heat sealer. The method for evaluating adhesion is to cut a test piece from this adhesive sheet, and use a tensile tester to measure the strength (g/15 mm) at the time of peeling by pulling it in a direction of 90 degrees to the adhesive surface at a pulling speed of 200 mm/min. He did what he asked for. In addition, as another adhesion evaluation criterion, in the case of samples coated on high-quality paper, the degree of destruction of the paper layer upon peeling was determined. The evaluation was performed according to the following criteria. 〇: Almost the entire paper layer is destroyed upon peeling, △: Partial paper layer is destroyed upon peeling, ×: No paper layer is destroyed at all upon peeling. The blocking resistance was evaluated by applying a load of 0.5 kg/cm 2 to the coated surfaces of aluminum foil (17ÎŒ) coated with approximately 5 g/m 2 (solid content) or to the coated and non-coated surfaces together. The film was left in a constant temperature and humidity environment of 30°C and 60% humidity, and after 24 hours, it was peeled off by hand to evaluate the degree of blocking. Evaluation of blocking resistance was performed according to the following criteria. 〇: Almost no tackiness △: Slight tackiness ×: Considerable tackiness Example 1 Consists of 92 mol% ethylene and 8 mol% methacrylic acid, with 29% of the methacrylic acid converted to sodium ions. Aqueous dispersion of the copolymer (solids concentration 40% by weight, viscosity
130cps, sodium oleate amount based on solid weight
(containing 0.5%), 5 parts of a diester compound shown in Table 1 was added to 100 parts by weight of the copolymer. The resulting aqueous dispersion was placed on aluminum foil at 6 g/ m2.
(solid content), and the thermal adhesion and blocking resistance at low temperatures of this heat-sensitive adhesive sheet were measured. For comparison, a sheet treated with a dispersion containing no diester compound was also measured. The results are shown in Table 1. As is clear from the table, the adhesive sheet treated with the dispersion of the present invention can be thermally bonded even at 75°C, and has significantly improved low-temperature adhesion compared to the comparative example, and also has good blocking resistance. It is also found that the combination of an aliphatic dibasic diester and a sulfosuccinic acid diester further improves the low-temperature heat adhesion.

【衚】 実斜䟋  ゚チレン91モルずアクリル酞モルの共重
合䜓のアンモニりム䞭和䞭和床100の分散
液固圢分濃床40重量に゜ゞりムスルホゞト
リデシルサクシネヌトを郚配合した。埗られた
分散物の熱接着性及び耐ブロツキング性は次ぎの
通りであ぀た。
[Table] Example 2 Sodium sulfoditridecyl succinate was added to an ammonium-neutralized (neutralization degree 100%) dispersion (solid content concentration 40% by weight) of a copolymer of 91 mol% ethylene and 9 mol% acrylic acid. 5 parts of was added. The thermal adhesion and blocking resistance of the obtained dispersion were as follows.

【衚】 実斜䟋  モルで92の組成比の゚チレンメタ
クリル酞メタクリル酞メチル゚ステルの共重合
䜓カルボン酞基の党量の玄65がナトリりムむ
オンで䞭和の分散液固圢分濃床40重量
に、ポリ゚ステル系アゞペヌトの乳化分散液、又
ポリ゚チレンセバケヌトの乳化分散液を玔分ずし
お共重合䜓100郚に察しお郚配合した。埗られ
た分散物の熱接着性及び耐ブロツキング性は次ぎ
の通りであ぀た。
[Table] Example 3 Dispersion of a copolymer of ethylene/methacrylic acid/methacrylic acid methyl ester with a composition ratio of 92/5/3 in mol% (approximately 65% of the total amount of carboxylic acid groups is neutralized with sodium ions) Liquid (solid content concentration 40% by weight)
7 parts of a pure emulsified dispersion of polyester adipate or an emulsified dispersion of polyethylene sebacate were added to 100 parts of the copolymer. The thermal adhesion and blocking resistance of the obtained dispersion were as follows.

【衚】 実斜䟋  ゚チレンずメタクリル酞の共重合䜓。共重合
割合95モルモルず゚チレンずアクリル
酞の共重合䜓共重合割合91モルモル
の二皮の共重合䜓より成り、二぀の共重合䜓の混
合割合が前者の共重合䜓埌者の共重合䜓7/3
重量比の分散液党共重合䜓の濃床は40重量
であり、共重合䜓の党カルボン酞基の玄30は
ナトリりムむオンで䞭和されおいるに、アれラ
むン酞ゞオクチルの乳化分散液を共重合䜓重量
100郚に察しお各々郚、10郚、15郚配合した。
埗られた分散物の熱接着性及び耐ブロツキング性
は次ぎの通りであ぀た。
[Table] Example 4 Copolymer of ethylene and methacrylic acid. (copolymerization ratio 95 mol%/5 mol%) and a copolymer of ethylene and acrylic acid (copolymerization ratio 91 mol%/9 mol%)
The mixing ratio of the two copolymers is former copolymer/latter copolymer = 7/3.
Emulsification of dioctyl azelaate in a dispersion (by weight) of Copolymerization weight of dispersion
5 parts, 10 parts, and 15 parts of each were added to 100 parts.
The thermal adhesion and blocking resistance of the obtained dispersion were as follows.

【衚】 添加量が倚すぎるず無添加にくらべ接着可胜最
䜎枩床はやはり䞋がるが、接着匷床が䜎くなる。
又、15郚添加した分散液は週間后に油滎状物が
みられるようになり、基材に塗垃した堎合均䞀な
塗膜が埗られなか぀た。 実斜䟋及び比范䟋 本比范䟋では本発明で芏定する゚チレン系共重
合䜓以倖の他の暹脂の分散液に本発明で甚いるゞ
゚ステル化合物を合しおも効果がないこずを䟋瀺
する。 ゞ゚ステル化合物ずしおアゞピン酞ゞオクチル
を甚い、分散液䞭の暹脂重量100郚に察し郚配
合した。配合后の分散液は䞊質玙に6gm2固
圢分塗垃し、その分散液塗垃玙の熱接着性詊隓
を行な぀た。尚、接着性の評䟡は接着面の剥離時
の玙局砎壊皋床を求めるこずで行な぀た。 その結果は衚に瀺す通りである。 衚から明らかな劂く本発明で甚いる暹脂以倖の
暹脂に配合しおも党く熱接着性が改良されない。
それに察しお本発明で芏定する暹脂に配合すれば
倧幅に改良されるこずが刀る。
[Table] If the amount added is too large, the minimum temperature at which bonding is possible will be lower than when no additive is added, but the bonding strength will be lower.
In addition, oil droplets appeared after one week in the dispersion to which 15 parts were added, and a uniform coating film could not be obtained when applied to a substrate. Example 5 and Comparative Example 1 This comparative example illustrates that there is no effect even if the diester compound used in the present invention is combined with a dispersion of a resin other than the ethylene copolymer defined in the present invention. Dioctyl adipate was used as a diester compound, and 5 parts were added to 100 parts of the resin weight in the dispersion. After blending, the dispersion was applied to high-quality paper at 6 g/m 2 (solid content), and the paper coated with the dispersion was subjected to a thermal adhesion test. The adhesiveness was evaluated by determining the degree of destruction of the paper layer when the adhesive surface was peeled off. The results are shown in Table 2. As is clear from the table, the thermal adhesiveness is not improved at all even when the resin is mixed with a resin other than the resin used in the present invention.
On the other hand, it can be seen that if it is blended with the resin specified in the present invention, it is significantly improved.

【衚】 実斜䟋及び比范䟋 本比范䟋では、本発明で芏定する゚チレン系共
重合䜓の分散䜓に本発明で甚いるゞ゚ステル化合
物以倖のものを配合しおも効果がないこずを䟋瀺
する。 実斜䟋で甚いたず同じ分散液に衚、衚に
瀺すような添加剀を分散液䞭の暹脂重量100郚に
察し郚又は10郚配合した。埗られた各配合分散
物を䞊質玙に玄5gm2固圢分塗垃しお、そ
の凊理シヌトを熱接着しお䜎枩熱接着性を調べ
た。 その結果を衚、及び衚に瀺す。本発明に䜿
甚する脂肪族二塩基酞ゞ゚ステルは通垞可塑剀ず
しお䜿甚されるが、衚に瀺す劂く他の可塑剀等
を配分しおも党く効果がみられない。 又、本発明に斌いお䜿甚するスルホコハク酞ゞ
゚ステルは通垞界面掻性剀ずしお䜿甚されるが、
衚に瀺す劂く他の皮々の界面掻性剀を配合しお
も同じく党く効果がみられない。同じスルホコハ
ク酞゚ステルであ぀おもモノ゚ステルの堎合には
効果がない。
[Table] Example 6 and Comparative Example 2 This comparative example illustrates that there is no effect even if a substance other than the diester compound used in the present invention is blended into the ethylene copolymer dispersion defined in the present invention. . Additives shown in Tables 3 and 4 were added to the same dispersion as used in Example 1 in an amount of 5 parts or 10 parts per 100 parts of the resin weight in the dispersion. Each of the obtained blended dispersions was coated on high-quality paper at a solid content of about 5 g/m 2 , and the treated sheets were thermally bonded to examine low-temperature thermal adhesion properties. The results are shown in Tables 3 and 4. The aliphatic dibasic acid diester used in the present invention is usually used as a plasticizer, but as shown in Table 3, no effect is observed even when other plasticizers are used. Furthermore, the sulfosuccinic acid diester used in the present invention is usually used as a surfactant, but
As shown in Table 4, no effect was observed even when various other surfactants were added. Even if the same sulfosuccinate ester is used, it has no effect in the case of a monoester.

【衚】【table】

【衚】【table】

【衚】 実斜䟋及び比范䟋3A― 特開昭54―18689号報で提案の感熱接着組成物
ず本発明のそれずの性胜比范に぀いお䟋瀺する。 衚に瀺す組成の分散物固圢分濃床40重量
、党おの共重合䜓はナトリりムむオン䞭和、䞭
和床30を䜜り、その分散物の熱接着性及び耐
ブロツキング性を評䟡した。その結果は衚に瀺
す通りである。
[Table] Example 7 and Comparative Examples 3A-C Comparison of performance between the heat-sensitive adhesive composition proposed in JP-A-18689 and that of the present invention is illustrated. A dispersion with the composition shown in Table 5 (solid content concentration 40% by weight, all copolymers were sodium ion neutralized, degree of neutralization 30%) was prepared, and the thermal adhesion and blocking resistance of the dispersion were evaluated. . The results are shown in Table 6.

【衚】【table】

【衚】 グリセリンの゚ステル配合品は共重合割合が10
モル以䞋の暹脂に配合した堎合比范䟋に
は効果がない。共重合割合が高い暹脂に配合した
堎合比范䟋には䜎枩での熱接着性が向䞊す
るが、本発明法のものに范べお著しく接着匷床が
䜎い。たた、軟化点の䜎い暹脂である為耐ブロツ
キング性もやゝ劣る。
[Table] The copolymerization ratio of glycerin ester blended products is 10.
There is no effect when it is blended in a resin of less than mol % (Comparative Example A). When blended with a resin having a high copolymerization ratio (Comparative Example C), the thermal adhesion at low temperatures is improved, but the adhesive strength is significantly lower than that of the method of the present invention. Furthermore, since it is a resin with a low softening point, its blocking resistance is also somewhat inferior.

Claims (1)

【特蚱請求の範囲】  97〜85モルの゚チレンず〜15モルの
αβ―゚チレン系䞍飜和カルボン酞、あるいは
該䞍飜和カルボン酞の䞀郚がアルキル゚ステルで
あるものずからなる゚チレン系共重合䜓であ぀
お、前蚘䞍飜和カルボン酞の少くずも10が䞭和
されおいる共重合䜓の少くずも皮ず、脂肪族二
塩基酞ゞ゚ステルの少くずも皮及び又はスル
ホコハク酞ゞ゚ステルの少くずも皮ずを䞻成分
ずする氎性分散物。  脂肪族二塩基酞ゞ゚ステルがアゞピン酞のゞ
゚ステル又はセバシン酞のゞ゚ステルである特蚱
請求の範囲第項蚘茉の分散物。  共重合䜓分が20―60重量である特蚱請求の
範囲第項蚘茉の分散物。  ゞ゚ステル分が―15重量郚共重合䜓分
100重量郚に察しである特蚱請求の範囲第項
蚘茉の分散物。  脂肪酞二塩基酞ゞ゚ステルずスルホコハク酞
ゞ゚ステルずの䜵甚の堎合の倫々の盞察比が
〜である特蚱請求の範囲第項蚘茉の分
散物。  97〜85モルの゚チレンず〜15モルの
αβ―゚チレン系䞍飜和カルボン酞、あるいは
該䞍飜和カルボン酞の䞀郚がアルキル゚ステルで
あるものずからなる゚チレン系共重合䜓であ぀
お、前蚘䞍飜和カルボン酞の少くずも10が䞭和
されおいる共重合䜓の少くずも皮ず、脂肪族二
塩基酞ゞ゚ステルの少くずも皮及び又はスル
ホコハク酞ゞ゚ステルの少くずも皮ずを䞻成分
ずする氎性分散物で凊理した感熱接着シヌト。  氎性分散物が固圢物で2gm2以䞊である特
蚱請求の範囲第項蚘茉のシヌト。
[Scope of Claims] 1 Consists of 97 to 85 mol% ethylene and 3 to 15 mol% α,β-ethylenically unsaturated carboxylic acid, or a portion of the unsaturated carboxylic acid is an alkyl ester At least one type of ethylene copolymer in which at least 10% of the unsaturated carboxylic acid is neutralized, at least one type of aliphatic dibasic acid diester and/or sulfosuccinic acid. An aqueous dispersion containing at least one acid diester as a main component. 2. The dispersion according to claim 1, wherein the aliphatic dibasic acid diester is an adipic acid diester or a sebacic acid diester. 3. The dispersion according to claim 1, wherein the copolymer content is 20-60% by weight. 4 Diester content is 2-15 parts by weight (copolymer content
100 parts by weight). 5 When a fatty acid dibasic acid diester and a sulfosuccinic acid diester are used in combination, the relative ratio of each is 1:
A dispersion according to claim 1 in which the ratio is 1 to 5:1. 6 An ethylene copolymer consisting of 97 to 85 mol% ethylene and 3 to 15 mol% α,β-ethylenically unsaturated carboxylic acid, or a part of the unsaturated carboxylic acid is an alkyl ester. at least one copolymer in which at least 10% of the unsaturated carboxylic acids are neutralized; and at least one aliphatic dibasic acid diester and/or at least one sulfosuccinic acid diester. A heat-sensitive adhesive sheet treated with an aqueous dispersion mainly composed of seeds. 7. The sheet according to claim 6, wherein the aqueous dispersion has a solid content of 2 g/m 2 or more.
JP2283080A 1980-02-27 1980-02-27 Aqueous dispersion and heat-sensitive adhesive sheet treated with the same Granted JPS56120780A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2283080A JPS56120780A (en) 1980-02-27 1980-02-27 Aqueous dispersion and heat-sensitive adhesive sheet treated with the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2283080A JPS56120780A (en) 1980-02-27 1980-02-27 Aqueous dispersion and heat-sensitive adhesive sheet treated with the same

Publications (2)

Publication Number Publication Date
JPS56120780A JPS56120780A (en) 1981-09-22
JPS6231015B2 true JPS6231015B2 (en) 1987-07-06

Family

ID=12093606

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2283080A Granted JPS56120780A (en) 1980-02-27 1980-02-27 Aqueous dispersion and heat-sensitive adhesive sheet treated with the same

Country Status (1)

Country Link
JP (1) JPS56120780A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005534745A (en) * 2002-07-30 2005-11-17 スタンファりザヌ、りィリアム・シヌ Plastisol / hot melt composite composition
JP2011516621A (en) * 2008-02-26 2011-05-26 リクアメルト コヌポレヌション Polymer composition capable of being pumped at room temperature activated by energy application and apparatus for activating and applying the composition

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62116680A (en) * 1985-11-15 1987-05-28 Nitto Electric Ind Co Ltd Pressure-sensitive adhesive composition
JP2568583B2 (en) * 1987-10-05 1997-01-08 䞭倮理化工業株匏䌚瀟 Manufacturing method of low temperature heat sealable laminated sheet

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005534745A (en) * 2002-07-30 2005-11-17 スタンファりザヌ、りィリアム・シヌ Plastisol / hot melt composite composition
JP4792223B2 (en) * 2002-07-30 2011-10-12 スタンファりザヌ、りィリアム・シヌ Plastisol / hot melt composite composition
JP2011516621A (en) * 2008-02-26 2011-05-26 リクアメルト コヌポレヌション Polymer composition capable of being pumped at room temperature activated by energy application and apparatus for activating and applying the composition

Also Published As

Publication number Publication date
JPS56120780A (en) 1981-09-22

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