JP5307334B2 - テルペン樹脂−及び炭化水素樹脂−系の界面活性剤並びに粘着性付与剤樹脂の水性分散物 - Google Patents
テルペン樹脂−及び炭化水素樹脂−系の界面活性剤並びに粘着性付与剤樹脂の水性分散物 Download PDFInfo
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- JP5307334B2 JP5307334B2 JP2006502404A JP2006502404A JP5307334B2 JP 5307334 B2 JP5307334 B2 JP 5307334B2 JP 2006502404 A JP2006502404 A JP 2006502404A JP 2006502404 A JP2006502404 A JP 2006502404A JP 5307334 B2 JP5307334 B2 JP 5307334B2
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- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 1
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- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
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- 125000000962 organic group Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 230000000865 phosphorylative effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920006112 polar polymer Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
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- 238000010926 purge Methods 0.000 description 1
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- 230000001105 regulatory effect Effects 0.000 description 1
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- 238000006467 substitution reaction Methods 0.000 description 1
- 230000001180 sulfating effect Effects 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
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- 238000005979 thermal decomposition reaction Methods 0.000 description 1
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- 238000005809 transesterification reaction Methods 0.000 description 1
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L71/02—Polyalkylene oxides
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- C08F8/00—Chemical modification by after-treatment
- C08F8/14—Esterification
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- C08F8/00—Chemical modification by after-treatment
- C08F8/46—Reaction with unsaturated dicarboxylic acids or anhydrides thereof, e.g. maleinisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2615—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen the other compounds containing carboxylic acid, ester or anhydride groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/08—Macromolecular additives
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J171/00—Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
- C09J171/02—Polyalkylene oxides
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/52—Natural or synthetic resins or their salts
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/05—Polymer mixtures characterised by other features containing polymer components which can react with one another
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- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
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- C09J2471/00—Presence of polyether
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2852—Adhesive compositions
Landscapes
- Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
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- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Polyethers (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Description
発明の分野
本発明は、一般的に界面活性剤に、更に具体的には、樹脂がラテックスと配合されて、水性粘着剤(waterborne adhesive)を与えることができる、粘着性付与剤樹脂(tackifier resin)の水性分散物を調製するために有用な界面活性剤に関する。
溶媒系粘着剤(solvent−based adhesive)を置換える改良された水性(即ち水に分散された)粘着剤の継続する開発は、その認められた健康及び環境の災害に由来する、溶媒の政府による規制によって大きく動機付けされている。結果として、水性粘着剤が、各種の基質をいっしょに粘着するために広範囲に使用されるようになっている。このような粘着剤は、しばしば高分子量の弾性体ラテックス(又はアクリル及びスチレン−ブタジエンゴムラテックスのような、ラテックスの混合物)、及び少なくとも一つの水に分散された粘着性付与剤樹脂の両方を含んでなる。粘着性付与剤樹脂を含まない官能性水性粘着剤を調製することも可能である。然しながら、粘着剤の商業的適用を可能にする各種の基質への粘着を示す粘着剤を経済的に製造するために、後者を含めることが一般的に必要である。
簡単には、本発明は、樹脂、特に粘着性付与剤樹脂を水中に分散するための用途を有し、ここで分散された粘着性付与剤樹脂は、次いで水性粘着剤を調製するために使用される界面活性剤を調製するための方法を指向する。本発明は、更に開示された方法を使用して調製される界面活性剤、並びに組成物、例えば開示された界面活性剤を含んでなる水性分散物及び粘着性組成物も指向する。
一つの側面において、本発明は、界面活性剤を調製するための方法に向けられる。この方法は、樹脂を選択することを含み、ここで、樹脂は、モノマーの重合残基含んでなり、そしてモノマーは、不飽和炭化水素であるか、又はそれを含む。選択された樹脂は、α,β−不飽和カルボン酸、又はその酸無水物或いはそのエステルと反応して、本明細書中で付加体とも呼ばれる、カルボニル含有樹脂を与える。次いで付加体は、カルボキシル反応性ポリ(アルキレンオキシド)、例えば、ヒドロキシル−又はアミン−末端のポリ(アルキレンオキシド)と反応して、或いはin situでポリ(アルキレンオキシド)を生じるようにアルキレンオキシドと反応して、本発明の界面活性剤を与える。その構造にもよるが、界面活性剤は、リン酸化又は硫酸化によって化学的に改質することができる。
無水マレイン酸のテルペン−ビニル芳香族樹脂との反応による付加体の調製
四つ口の1Lの丸底フラスコに、450グラムのSylvares(登録商標)ZT105LTテルペン−ビニル芳香族樹脂(Arizona Chemical Company,Jacksonville,Florida)を入れ、そして2L/分の窒素置換下で150℃で加熱した。樹脂が溶融し、そして十分に流動性となった時点で、約250rpmで撹拌を始めた。撹拌された樹脂に、50.0グラムの無水マレイン酸を加えた。フラスコの内容物を窒素雰囲気下に置き、そして200℃に加熱した。撹拌を300rpmに増加した。反応物を16.5時間200℃で撹拌し、次いで250℃で約5.5時間加熱した。試料を分析し、97.1%の無水マレイン酸の転換が示された。温度を200℃まで下げ、そしてフラスコの内容物を窒素で散布して、未反応の無水マレイン酸を、水抽出物(試料と等重量)の酸価が0.3になるまで除去した。フラスコの内容物を排出した。付加体の分析は、6.54重量%の無水マレイン酸が付加されたことを示した。
実施例1の付加体のポリエチレングリコールとの反応による樹脂分散物界面活性剤の調製
パドル撹拌機、窒素の入り口及び熱電対を備えた、1Lの四つ口丸底フラスコに、100.0グラムの実施例1からの付加体及び143.2グラムの2000の平均分子量を有するポリエチレングリコール(“PEG2000”、Aldrich Chemical Company,Milwaukee,Wisconsin)を入れた。フラスコの内容物を、1L/分の窒素置換下で加熱した。内容物が溶融し、そして十分に流動性となった時点で撹拌を開始した。温度が219℃に達した時点で、0.54グラムの75%リン酸を入れ、そしてフラスコを窒素雰囲気下に置き、そして250℃に加熱した。反応物をこの温度で20時間撹拌した。反応物の試料は、1.4の酸価を有していた。フラスコの内容物を157℃に冷却し、そして排出した。
ロジンエステル粘着性付与剤樹脂の、実施例2の界面活性剤との分散物
1.5Lの樹脂フラスコに、300.0グラムのSylvares(登録商標)RE−85(Arizona Chemical Company,Jacksonville,FL)及び18.0グラムの実施例2からの界面活性剤を入れた。内容物を2L/分の窒素掃引下で98℃で加熱した。撹拌を開始し、そしてフラスコを窒素ブランケット下に置いた。2.1グラムの50%水酸化カリウムの、47グラムの蒸留水中の溶液を調製し、そして80℃に加熱した。粘着性付与剤樹脂−界面活性剤の配合物の温度が112℃になった時点で、熱水酸化カリウム溶液を加えて、まず油中水分散物を製造し、これは水中油分散物に反転した。この分散物の温度を97℃にし、そして160グラムの熱蒸留水を18分かけて加えた。得られた希釈された分散物を59℃に冷却し、そしてある程度の殺生物剤を加えた。更に50℃に冷却後、分散物を分析し、9.5のpHを得た。分散物の試料を7.5のpHに調節し、そして58.8%の固体及び0.84ミクロンの平均粒子の大きさであった。
Claims (30)
- 界面活性剤を調製するための方法であって、
α,β−不飽和カルボン酸又は酸無水物、或いはそのエステルを、炭化水素モノマー残基を含む樹脂と反応させて、付加体を提供し;
前記付加体を、アルキレンオキシド又はカルボキシル反応性ポリ(アルキレンオキシド)のいずれかと反応させて、界面活性剤を提供し;そして
前記界面活性剤を、リン酸化又はスルホン化のいずれかによって改質して、官能化された界面活性剤を得る
ことを含み、
前記樹脂が、テルペン−フェノール樹脂であり、そしてα−ピネン、β−ピネン、δ−3−カレン及びリモネンからなる群からそれぞれ独立に選択される一個以上のモノマー残基、並びに、スチレン、インデン、α−メチルスチレン、アルキル芳香族スチレン、ジビニルベンゼン、一つ又はそれより多いアルキル基を伴うジビニルベンゼンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を含むことを特徴とする方法。 - 前記α,β−不飽和カルボン酸が、マレイン酸であり、そしてα,β−不飽和カルボン酸無水物が、無水マレイン酸である、請求項1に記載の方法。
- 前記テルペン−フェノール樹脂が、イソブチレン、ジイソブチレン、1−アルケン、2−アルケン、三置換アルケン、ビニルシクロヘキセン、ピペリレン、イソプレン、2−メチル−2−ブテン、2−メチル−1−ブテン、シクロペンテン、非環式ペンテン、シクロペンタジエン、及びジシクロペンタジエンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を更に含む、請求項1に記載の方法。
- 前記フェノールが、フェノール、一置換フェノール、二置換フェノール、三置換フェノール及びヒドロキシル置換ナフタレン化合物からなる群からそれぞれ独立に選択される、請求項1に記載の方法。
- 前記付加体が、ポリ(エチレングリコール)又は一つより多いポリ(エチレングリコール)の混合物と反応させられる、請求項1に記載の方法。
- 前記付加体が、エチレンオキシドと反応させられる、請求項1に記載の方法。
- 請求項1に記載の方法により製造された界面活性剤。
- 請求項1に記載の方法により製造された界面活性剤及び粘着性付与剤樹脂を含む組成物。
- 請求項1に記載の方法により製造された界面活性剤、粘着性付与剤樹脂、ポリマーラテックス、及び水を含む粘着性組成物。
- 水並びに界面活性剤及び粘着性付与剤樹脂を含む組成物を含む水性分散物であって、
前記界面活性剤は、
α,β−不飽和カルボン酸又は酸無水物、或いはそのエステルを、炭化水素モノマー残基を含む樹脂と反応させて、付加体を提供し;そして
前記付加体を、アルキレンオキシド又はカルボキシル反応性ポリ(アルキレンオキシド)のいずれかと反応させて、界面活性剤を提供する
ことを含む方法により調製され、
前記樹脂が、テルペン−フェノール樹脂であり、そしてα−ピネン、β−ピネン、δ−3−カレン及びリモネンからなる群からそれぞれ独立に選択される一個以上のモノマー残基、並びに、スチレン、インデン、α−メチルスチレン、アルキル芳香族スチレン、ジビニルベンゼン、一つ又はそれより多いアルキル基を伴うジビニルベンゼンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を含むことを特徴とする、前記水性分散物。 - 前記方法が、前記界面活性剤剤をリン酸化又はスルホン化のいずれかによって改質して、官能化された界面活性剤を得ることを更に含む、請求項10に記載の水性分散物。
- 前記α,β−不飽和カルボン酸が、マレイン酸であり、そしてα,β−不飽和カルボン酸無水物が、無水マレイン酸である、請求項10に記載の水性分散物。
- 前記テルペン−フェノール樹脂が、イソブチレン、ジイソブチレン、1−アルケン、2−アルケン、三置換アルケン、ビニルシクロヘキセン、ピペリレン、イソプレン、2−メチル−2−ブテン、2−メチル−1−ブテン、シクロペンテン、非環式ペンテン、シクロペンタジエン、及びジシクロペンタジエンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を更に含む、請求項10に記載の水性分散物。
- 前記フェノールが、フェノール、一置換フェノール、二置換フェノール、三置換フェノール及びヒドロキシル置換ナフタレン化合物からなる群からそれぞれ独立に選択される、請求項10に記載の水性分散物。
- 前記樹脂が、ピペリレン、イソプレン、2−メチル−2−ブテン、2−メチル−1−ブテン、シクロペンテン、非環式ペンテン、シクロペンタジエン、及びジシクロペンタジエンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を含む、請求項10に記載の水性分散物。
- 前記付加体が、ポリ(エチレングリコール)又は一つより多いポリ(エチレングリコール)の混合物と反応させられる、請求項10に記載の水性分散物。
- 前記付加体が、エチレンオキシドと反応させられる、請求項10に記載の水性分散物。
- 界面活性剤、粘着性付与剤樹脂、ポリマーラテックス、及び水を含む粘着性組成物であって、
前記界面活性剤が、
α,β−不飽和カルボン酸又は酸無水物、或いはそのエステルを、炭化水素モノマー残基を含む樹脂と反応させて、付加体を提供し;そして
前記付加体を、アルキレンオキシド又はカルボキシル反応性ポリ(アルキレンオキシド)のいずれかと反応させて、界面活性剤を提供する
ことを含む方法により調製され、
前記樹脂が、テルペン−フェノール樹脂であり、そしてα−ピネン、β−ピネン、δ−3−カレン及びリモネンからなる群からそれぞれ独立に選択される一個以上のモノマー残基、並びに、スチレン、インデン、α−メチルスチレン、アルキル芳香族スチレン、ジビニルベンゼン、一つ又はそれより多いアルキル基を伴うジビニルベンゼンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を含むことを特徴とする、前記粘着性組成物。 - 前記方法が、前記界面活性剤剤をリン酸化又はスルホン化のいずれかによって改質して、官能化された界面活性剤を得ることを更に含む、請求項18に記載の粘着性組成物。
- 前記α,β−不飽和カルボン酸が、マレイン酸であり、そしてα,β−不飽和カルボン酸無水物が、無水マレイン酸である、請求項18に記載の粘着性組成物。
- 前記テルペン−フェノール樹脂が、イソブチレン、ジイソブチレン、1−アルケン、2−アルケン、三置換アルケン、ビニルシクロヘキセン、ピペリレン、イソプレン、2−メチル−2−ブテン、2−メチル−1−ブテン、シクロペンテン、非環式ペンテン、シクロペンタジエン、及びジシクロペンタジエンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を更に含む、請求項18に記載の粘着性組成物。
- 前記フェノールが、フェノール、一置換フェノール、二置換フェノール、三置換フェノール及びヒドロキシル置換ナフタレン化合物からなる群からそれぞれ独立に選択される、請求項18に記載の粘着性組成物。
- 前記付加体が、ポリ(エチレングリコール)又は一つより多いポリ(エチレングリコール)の混合物と反応させられる、請求項18に記載の粘着性組成物。
- 前記付加体が、エチレンオキシドと反応させられる、請求項18に記載の粘着性組成物。
- 粘着性組成物の層を基質の表面に適用し、そして前記層を乾燥することによって調製される、感圧粘着性オーバーレイであって、前記粘着性組成物が、界面活性剤、粘着性付与剤樹脂、ポリマーラテックス、及び水を含み、
前記界面活性剤が、
α,β−不飽和カルボン酸又は酸無水物、或いはそのエステルを、炭化水素モノマー残基を含む樹脂と反応させて、付加体を提供し;そして
前記付加体を、アルキレンオキシド又はカルボキシル反応性ポリ(アルキレンオキシド)のいずれかと反応させて、界面活性剤を提供する
ことを含む方法により調製され、
前記樹脂が、テルペン−フェノール樹脂であり、そしてα−ピネン、β−ピネン、δ−3−カレン及びリモネンからなる群からそれぞれ独立に選択される一個以上のモノマー残基、並びに、スチレン、インデン、α−メチルスチレン、アルキル芳香族スチレン、ジビニルベンゼン、一つ又はそれより多いアルキル基を伴うジビニルベンゼンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を含むことを特徴とする、前記感圧粘着性オーバーレイ。 - 前記α,β−不飽和カルボン酸が、マレイン酸であり、そしてα,β−不飽和カルボン酸無水物が、無水マレイン酸である、請求項25に記載の感圧粘着性オーバーレイ。
- 前記テルペン−フェノール樹脂が、イソブチレン、ジイソブチレン、1−アルケン、2−アルケン、三置換アルケン、ビニルシクロヘキセン、ピペリレン、イソプレン、2−メチル−2−ブテン、2−メチル−1−ブテン、シクロペンテン、非環式ペンテン、シクロペンタジエン、及びジシクロペンタジエンからなる群からそれぞれ独立に選択される一個以上のモノマー残基を更に含む、請求項25に記載の感圧粘着性オーバーレイ。
- 前記フェノールが、フェノール、一置換フェノール、二置換フェノール、三置換フェノール及びヒドロキシル置換ナフタレン化合物からなる群からそれぞれ独立に選択される、請求項25に記載の感圧粘着性オーバーレイ。
- 前記付加体が、ポリ(エチレングリコール)又は一つより多いポリ(エチレングリコール)の混合物と反応させられる、請求項25に記載の感圧粘着性オーバーレイ。
- 前記付加体が、エチレンオキシドと反応させられる、請求項25に記載の感圧粘着性オーバーレイ。
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US6228944B1 (en) * | 1999-06-24 | 2001-05-08 | The Goodyear Tire & Rubber Company | Polymeric resinous material derived from limonene, dimethyl-dicyclopentadiene, indene and vinyl toluene |
US6369146B1 (en) | 1999-10-26 | 2002-04-09 | Air Products And Chemicals, Inc. | Malic acid diester surfactants |
JP2002011337A (ja) | 2000-06-28 | 2002-01-15 | Harima Chem Inc | 水性エマルション用乳化分散剤 |
US6461728B2 (en) | 2000-12-29 | 2002-10-08 | 3M Innovative Properties Company | Gamma radiation polymerized emulsion-based (meth)acrylate pressure sensitive adhesives and methods of making and using same |
US6900274B2 (en) * | 2003-02-06 | 2005-05-31 | Arizona Chemical Company | Terpene resin-and hydrocarbon resin-based surfactants and aqueous dispersion of tackifier resins |
-
2003
- 2003-02-06 US US10/360,585 patent/US6900274B2/en not_active Expired - Lifetime
-
2004
- 2004-01-28 WO PCT/IB2004/000300 patent/WO2004069952A2/en active Application Filing
- 2004-01-28 EP EP04705867A patent/EP1597333B1/en not_active Expired - Lifetime
- 2004-01-28 ES ES04705867T patent/ES2350635T3/es not_active Expired - Lifetime
- 2004-01-28 JP JP2006502404A patent/JP5307334B2/ja not_active Expired - Fee Related
- 2004-01-28 AT AT04705867T patent/ATE477314T1/de not_active IP Right Cessation
- 2004-01-28 DE DE602004028578T patent/DE602004028578D1/de not_active Expired - Lifetime
- 2004-01-28 CN CN2008100019426A patent/CN101274241B/zh not_active Expired - Fee Related
- 2004-01-28 CN CNB2004800037320A patent/CN100366698C/zh not_active Expired - Fee Related
- 2004-08-10 US US10/915,113 patent/US20050096436A1/en not_active Abandoned
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2007
- 2007-01-29 US US11/699,203 patent/US7452941B2/en not_active Expired - Fee Related
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2011
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Also Published As
Publication number | Publication date |
---|---|
CN101274241B (zh) | 2012-01-11 |
US20070207313A1 (en) | 2007-09-06 |
EP1597333B1 (en) | 2010-08-11 |
US20040158003A1 (en) | 2004-08-12 |
US7452941B2 (en) | 2008-11-18 |
ATE477314T1 (de) | 2010-08-15 |
US20050096436A1 (en) | 2005-05-05 |
WO2004069952A3 (en) | 2004-09-16 |
WO2004069952A2 (en) | 2004-08-19 |
US6900274B2 (en) | 2005-05-31 |
JP2006518791A (ja) | 2006-08-17 |
JP2011252156A (ja) | 2011-12-15 |
DE602004028578D1 (de) | 2010-09-23 |
EP1597333A2 (en) | 2005-11-23 |
CN1748013A (zh) | 2006-03-15 |
ES2350635T3 (es) | 2011-01-25 |
CN100366698C (zh) | 2008-02-06 |
CN101274241A (zh) | 2008-10-01 |
JP5650069B2 (ja) | 2015-01-07 |
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