JPWO2015188947A5 - - Google Patents
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- JPWO2015188947A5 JPWO2015188947A5 JP2016572295A JP2016572295A JPWO2015188947A5 JP WO2015188947 A5 JPWO2015188947 A5 JP WO2015188947A5 JP 2016572295 A JP2016572295 A JP 2016572295A JP 2016572295 A JP2016572295 A JP 2016572295A JP WO2015188947 A5 JPWO2015188947 A5 JP WO2015188947A5
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- 239000011248 coating agent Substances 0.000 claims description 34
- 238000000576 coating method Methods 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 24
- 229920001577 copolymer Polymers 0.000 claims description 14
- 239000001993 wax Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 230000001070 adhesive Effects 0.000 claims description 10
- 229920001971 elastomer Polymers 0.000 claims description 6
- 239000000806 elastomer Substances 0.000 claims description 5
- 229920000098 polyolefin Polymers 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 4
- 229920001400 block copolymer Polymers 0.000 claims description 4
- 238000003618 dip coating Methods 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 238000002844 melting Methods 0.000 claims description 4
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 229920000193 polymethacrylate Polymers 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 4
- 239000011118 polyvinyl acetate Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 230000000111 anti-oxidant Effects 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 3
- 239000000155 melt Substances 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- 230000002411 adverse Effects 0.000 claims description 2
- 238000007766 curtain coating Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- 239000003921 oil Substances 0.000 claims description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- 239000004831 Hot glue Substances 0.000 claims 1
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 1
- 239000002318 adhesion promoter Substances 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 238000001704 evaporation Methods 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 239000003205 fragrance Substances 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 238000000465 moulding Methods 0.000 claims 1
- 238000005453 pelletization Methods 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 238000003825 pressing Methods 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 description 5
- 230000003197 catalytic Effects 0.000 description 4
- -1 polypropylene Polymers 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229920002383 APAO Polymers 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- BLDFSDCBQJUWFG-UHFFFAOYSA-N 2-(methylamino)-1,2-diphenylethanol Chemical compound C=1C=CC=CC=1C(NC)C(O)C1=CC=CC=C1 BLDFSDCBQJUWFG-UHFFFAOYSA-N 0.000 description 1
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000273930 Brevoortia tyrannus Species 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N Ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene (PE) Substances 0.000 description 1
- 229920000468 Polystyrene-block-polybutadiene-block-polystyrene Polymers 0.000 description 1
- 239000004708 Very-low-density polyethylene Substances 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical group 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QYMGIIIPAFAFRX-UHFFFAOYSA-N butyl prop-2-enoate;ethene Chemical compound C=C.CCCCOC(=O)C=C QYMGIIIPAFAFRX-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000012716 cod liver oil Nutrition 0.000 description 1
- 239000003026 cod liver oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 235000019688 fish Nutrition 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 239000000289 melt material Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001098 polystyrene-block-poly(ethylene/propylene) Polymers 0.000 description 1
- 229920002742 polystyrene-block-poly(ethylene/propylene) -block-polystyrene Polymers 0.000 description 1
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000001681 protective Effects 0.000 description 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 description 1
- 231100000185 significant adverse effect Toxicity 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
Description
上記の技術的課題の解決は、特許請求の範囲にて特徴付けられる実施の形態を提供することにより達成される。特に本発明は、コーティングを有するHMA塊を作製する方法であって、該コーティングは50℃まで不粘着特性を有し、上記方法は液体形態又は溶融形態で存在するコーティング材料を固体形態で存在するHMA塊の表面に少なくとも部分的に塗布する工程を含み、塗布する該コーティング材料は該HMA塊の表面上にて60秒以内、好ましくは30秒以内であるが、少なくとも0.1秒以上、例えば0.1秒~30秒で固化及び固定してコーティングを形成する、方法を提供する。本発明によると、「HMA塊」、「HMA材料」及び「HMA配合物」という用語はそれぞれ、好ましくはHMPSA群を含み、すなわち好ましい実施の形態では、本明細書で使用される「HMA塊」又は「HMA材料」又は「HMA配合物」という用語は「HMPSA塊」又は「HMPSA材料」又は「HMPSA配合物」という用語に置き換えることができる。その上、或る特定温度(T)までの「不粘着」及び「不粘着特性」という用語は、材料が言及される温度(T)未満にて通例(包装、操作者の手等が)接する表面に付着しないことを意味する。一般に、上記特性はコーティングを有するHMAのブロック同士が互いに触れている段ボール箱内に材料を入れることにより評価することができる。箱を閉じ、1週間、言及される温度にてオーブンに入れる。次いで、箱をオーブンから取り出し、室温にて平衡化させる。その後、コーティング処理されたHMAの各ブロックを、隣接するブロック、保護紙又は操作者の手に付着することなく、手で個々に容易に取り出すことができる場合、コーティングを不粘着であると評価する。
The solution to the above technical problems is achieved by providing embodiments characterized in the claims. In particular, the present invention is a method for producing an HMA mass having a coating, wherein the coating has a non-adhesive property up to 50 ° C., and the above method exists as a coating material existing in a liquid form or a melt form in a solid form. It comprises the step of at least partially applying to the surface of the HMA mass, the coating material to be applied being on the surface of the HMA mass within 60 seconds, preferably within 30 seconds, but at least 0.1 seconds or more, eg. Provided is a method of solidifying and fixing in 0.1 to 30 seconds to form a coating. According to the present invention, the terms "HMA mass", "HMA material" and "HMA formulation" each preferably preferably include the HMPSA group, i.e., in a preferred embodiment, the "HMA mass" as used herein. Alternatively, the term "HMA material" or "HMA formulation" can be replaced with the term "HMPSA mass" or "HMPSA material" or "HMPSA formulation". Moreover, the terms "non-adhesive" and "non-adhesive property" up to a certain temperature (T) usually come into contact (packaging, operator's hands, etc.) below the temperature (T) at which the material is mentioned. It means that it does not adhere to the surface. In general, the above properties can be evaluated by placing the material in a cardboard box in which the blocks of HMA having a coating are in contact with each other. Close the box and place in the oven at the temperature mentioned for 1 week. The box is then removed from the oven and equilibrated at room temperature. The coating is then evaluated as non-adhesive if each block of coated HMA can be easily removed individually by hand without sticking to adjacent blocks, protective paper or operator's hands. ..
コーティング材料は、50℃まで不粘着特性を有するとともに、ワックス又はその派生物、エチレン系(コ)ポリマー、ポリオレフィン、ポリ酢酸ビニル及びそのコポリマー、ポリ(メタ)アクリレート、ポリエステル、ポリビニルアルコール、ポリウレタン、ビニルモノマーとポリアルキレンオキシドとのコポリマー、エラストマーブロックコポリマー、及びそれらのブレンド又は混合物からなる群から選択される複数の構成要素の内の1つを含み得る。さらにコーティング材料は、任意の構成要素/成分として可塑剤、安定剤及び抗酸化剤からなる群から選択される1つ又は複数の構成要素/成分を含有し得る。コーティング材料は原則としてコーティングとして存在する場合の50℃まで上記不粘着特性を除けば何ら制限はないが、エンドユーザー/顧客が更に塗布するためにコーティングを有するHMA塊を溶融させる場合にHMAの(予測される)特性に悪影響(すなわち大きな有害作用)をもたらさないように選択することが好まれ得る。コーティング材料は、例えばスプレーコーティング、カーテンコーティング又は浸漬コーティング等の当該技術分野に既知の任意の方法により塗布することができ、スプレーコーティングが好ましい。浸漬コーティングでは、HMA塊を浸漬する期間は0.1秒~30秒の期間内であることが好ましい。コーティング材料をHMA塊の表面に塗布した後、任意に例えば0.1秒~10秒間に、好ましくは150℃~250℃の温度にて急速加熱することによりコーティングの形成を促すことができる。さらに塗布されたコーティングを室温(約25℃)に冷却し、例えばすぐ使用することができる状態でコーティングを有するHMA塊を得ることができる。
The coating material has non-adhesive properties up to 50 ° C., wax or its derivatives, ethylene-based (co) polymers, polyolefins, polyvinyl acetate and its copolymers, poly (meth) acrylates, polyesters, polyvinyl alcohols, polyurethanes, vinyls. It may include one of a plurality of components selected from the group consisting of copolymers of monomers and polyalkylene oxides, elastomer block copolymers, and blends or mixtures thereof. Further, the coating material may contain, as any component / component, one or more components / components selected from the group consisting of plasticizers, stabilizers and antioxidants. The coating material is not limited in principle up to 50 ° C. when present as a coating, except for the non-adhesive properties described above, but when the end user / customer melts the HMA mass having the coating for further application of the HMA ( It may be preferred to choose so as not to adversely affect (ie, significant adverse effects) the properties (predicted). The coating material can be applied by any method known in the art, such as spray coating, curtain coating or dip coating, and spray coating is preferred. In the dip coating, the period for dipping the HMA mass is preferably within a period of 0.1 to 30 seconds. After the coating material is applied to the surface of the HMA mass, the formation of the coating can be promoted by rapidly heating it arbitrarily, for example, for 0.1 second to 10 seconds, preferably at a temperature of 150 ° C. to 250 ° C. Further, the applied coating can be cooled to room temperature (about 25 ° C.) to obtain an HMA mass having the coating, for example ready to use.
本発明の方法に使用されるコーティング材料は任意の熱可塑性材料とすることができるが、50℃まで不粘着特性を有するものとする。コーティング材料はホットメルト材料であることが好ましい。コーティング材料は、融点が約54℃~85℃のパラフィンワックス及び融点が約54℃~95℃の微結晶ワックス(後者の融点はDSC法によって求められる)等の石油ワックス、ASTM E-28によって求められる環球式軟化点が約120℃~160℃のアタクチックポリプロピレン、メタロセン触媒のプロピレン系ワックス、メタロセン触媒のワックス又はシングルサイト触媒のワックス、フィッシャー-トロプシュワックス等の一酸化炭素と水素とを重合させることにより作製される合成ワックス、並びにポリオレフィンワックスを含む、ワックス及びその派生物から選択することができる。これらのワックスはそれぞれ室温で固体である。他の有用な物質/成分としては、接着剤業界にて「動物ワックス又は植物ワックス」と呼ばれるものが挙げられ、その例には、限定されるものではないが、水素化された動物性、魚性及び植物性の油脂、例えば水素化された獣脂、ラード、ダイズ油、綿実油、ヒマシ油、メンハーデン油、タラ肝油等があり、これらは水素化しているために周囲温度で固体である。これらはワックス材料と同等に機能することからも有用であることが分かっている。有用な部分的に結晶性のエチレン系ポリマーの中でも、チーグラー・ナッタ触媒重合により得られるLDPE、VLDPE、LLDPE、MDPE、又は気相ランダム重合により得られるLDPE、EVA、EAA、EMA、EBA、EE2HA、又はチーグラー・ナッタ触媒重合若しくはシングルサイト触媒重合若しくはメタロセン触媒重合により得られるEO、EP、EB、EH、ESIコポリマーに言及することができる。加えて、エチレンメタクリレート、エチレンn-ブチルアクリレート及びエチレンアクリル酸ポリマーのような他のエチレンコポリマー;ポリエチレン、ポリプロピレン及びコポリマー、非晶質ポリ-α-オレフィン(APAO)等のポリオレフィン;ポリ酢酸ビニル及びコポリマー;様々なアクリル系モノマー由来のポリ(メタ)アクリレート、例えばアルキル(メタ)アクリレート、ヒドロキシアルキル(メタ)アクリレート、アクリルアミド;ポリエステル;ポリビニルアルコール;ポリウレタン;ビニルモノマーとポリアルキレンオキシドとのコポリマーに言及することができる。他の有用な物質としては、SB、SI、SBS、SIS、SEBS、SEPS及びSEPを含むエラストマーブロックコポリマーが挙げられる。有用なエラストマーはエチレンとプロピレンとのエラストマーコポリマー、又は官能性モノマーで修飾されたこのようなコポリマーである。例には、EPRゴム、EPDMゴム及び/又はEPRとEPDMとのブレンドがある。官能性モノマーとしては、カルボン酸基、無水物基、ヒドロキシル基、エーテル基、第一級、第二級及び第三級アミン基、並びにエステル基を含む1つ又は複数の官能基を含有する不飽和有機化合物群が挙げられる。
The coating material used in the method of the present invention may be any thermoplastic material, but shall have non-adhesive properties up to 50 ° C. The coating material is preferably a hot melt material. The coating material is determined by ASTM E-28, a petroleum wax such as paraffin wax having a melting point of about 54 ° C. to 85 ° C. and microcrystalline wax having a melting point of about 54 ° C. to 95 ° C. (the latter melting point is determined by the DSC method). Carbon monoxide such as atactic polypropylene having a ring-shaped softening point of about 120 ° C. to 160 ° C., a propylene-based wax of a metallocene catalyst, a wax of a metallocene catalyst or a wax of a single-site catalyst, and Fisher-Tropsch wax is polymerized with hydrogen. It can be selected from waxes and derivatives thereof, including synthetic waxes thus produced, as well as polyolefin waxes. Each of these waxes is solid at room temperature. Other useful substances / ingredients include, but are not limited to, hydrogenated animal, fish, which are referred to in the adhesive industry as "animal wax or vegetable wax". There are sex and vegetable fats and oils such as hydrogenated tallow, lard, soybean oil, cottonseed oil, castor oil, Menhaden oil, cod liver oil and the like, which are solid at ambient temperature because they are hydrogenated. They have also been found to be useful because they function in the same way as wax materials. Among the useful partially crystalline ethylene polymers, LDPE, VLDPE, LLDPE, MDPE obtained by Ziegler-Natta catalytic polymerization, or LDPE, EVA, EAA, EMA, EBA, EE2HA obtained by vapor phase random polymerization, Alternatively, reference can be made to EO, EP, EB, EH, ESI copolymers obtained by Ziegler-Natta catalytic polymerization or single site catalytic polymerization or metallocene catalytic polymerization. In addition, other ethylene copolymers such as ethylene methacrylate, ethylene n-butyl acrylate and ethylene acrylate polymers; polyolefins such as polyethylene, polypropylene and copolymers, amorphous poly-α-olefin (APAO); polyvinyl acetate and copolymers. References to poly (meth) acrylates derived from various acrylic monomers, such as alkyl (meth) acrylates, hydroxyalkyl (meth) acrylates, acrylamides; polyesters; polyvinyl alcohols; polyurethanes; copolymers of vinyl monomers and polyalkylene oxides. Can be done. Other useful materials include elastomer block copolymers containing SB, SI, SBS, SIS, SEBS, SEPS and SEP. Useful elastomers are elastomer copolymers of ethylene and propylene, or such copolymers modified with functional monomers. Examples include EPR rubber, EPDM rubber and / or blends of EPR and EPDM. The functional monomer contains one or more functional groups including a carboxylic acid group, an anhydride group, a hydroxyl group, an ether group, a primary, secondary and tertiary amine group, and an ester group. A group of saturated organic compounds can be mentioned.
Claims (9)
前記コーティング材料を塗布する工程において、前記HMPSA粒のブロックの表面温度が-20℃~40℃の範囲である、方法。 A method of making a hot melt adhesive (HMPSA) with a coating, the coating having non-adhesive properties up to 50 ° C., the method of pelletizing HMPSA and obtaining HMPSA granules in a mold hole. The step of obtaining a block of HMPSA grains by molding with or without pressure, and the coating material present in liquid or molten form at least partially on the surface of the block of HMPSA grains present in solid form. The coating material to be applied is a method of solidifying and fixing on the surface of a block of HMPSA grains within 60 seconds to form a coating.
A method in which the surface temperature of the block of HMPSA grains is in the range of −20 ° C. to 40 ° C. in the step of applying the coating material.
ペレット化形態及び/又は成形された形態で存在する前記HMPSAを蒸発及び/又は加熱により乾燥する工程と、
任意に、ペレット化形態及び/又は成形された形態及び/又は乾燥形態で存在する前記HMPSAの形状を、圧力を印加することにより固定する工程と、
を含む、請求項1~7のいずれか一項に記載の方法。 In the step of obtaining a block of HMPSA grains before the step of applying the coating material, the following steps are further:
The step of drying the HMPSA existing in the pelletized form and / or the molded form by evaporation and / or heating, and
Optionally, a step of fixing the shape of the HMPSA present in pelletized and / or molded and / or dried forms by applying pressure.
The method according to any one of claims 1 to 7, comprising the method according to any one of claims 1 to 7.
HMPSA with a coating, the coating having non-adhesive properties up to 50 ° C., the HMPSA being a block of HMPSA grains.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EPEP14002028 | 2014-06-12 | ||
EP14002028.0A EP2954995B1 (en) | 2014-06-12 | 2014-06-12 | Process for preparing hot melt pressure sensitive adhesive (HMPSA) having a tack-free coating |
PCT/EP2015/001193 WO2015188947A1 (en) | 2014-06-12 | 2015-06-12 | Process for preparing hma having a tack-free coating |
Related Child Applications (1)
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JP2020153493A Division JP2021001347A (en) | 2014-06-12 | 2020-09-14 | Method for manufacturing hma having non-adhesive coating |
Publications (3)
Publication Number | Publication Date |
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JP2017524513A JP2017524513A (en) | 2017-08-31 |
JPWO2015188947A5 true JPWO2015188947A5 (en) | 2022-05-10 |
JP7093157B2 JP7093157B2 (en) | 2022-06-29 |
Family
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Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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JP2016572295A Active JP7093157B2 (en) | 2014-06-12 | 2015-06-12 | How to make an HMA with a non-adhesive coating |
JP2020153493A Pending JP2021001347A (en) | 2014-06-12 | 2020-09-14 | Method for manufacturing hma having non-adhesive coating |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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JP2020153493A Pending JP2021001347A (en) | 2014-06-12 | 2020-09-14 | Method for manufacturing hma having non-adhesive coating |
Country Status (17)
Country | Link |
---|---|
US (1) | US10486190B2 (en) |
EP (1) | EP2954995B1 (en) |
JP (2) | JP7093157B2 (en) |
KR (1) | KR102398442B1 (en) |
CN (1) | CN106459715B (en) |
AU (1) | AU2015273903A1 (en) |
BR (1) | BR112016028868A2 (en) |
CA (1) | CA2951740A1 (en) |
DK (1) | DK2954995T3 (en) |
ES (1) | ES2614285T3 (en) |
IL (1) | IL249097B (en) |
MX (1) | MX2016015622A (en) |
PL (1) | PL2954995T3 (en) |
PT (1) | PT2954995T (en) |
RU (1) | RU2688853C2 (en) |
SG (1) | SG11201609895TA (en) |
WO (1) | WO2015188947A1 (en) |
Family Cites Families (21)
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DE3410957A1 (en) | 1984-03-24 | 1985-09-26 | Henkel KGaA, 4000 Düsseldorf | AQUEOUS RELEASE AGENTS |
FR2601616B1 (en) * | 1986-07-21 | 1989-06-02 | Ceca Sa | NEW PROCESS FOR OBTAINING SELF-ADHESIVE BLOCKS WITH NON-ADHESIVE SURFACE. |
US5041251A (en) | 1989-07-27 | 1991-08-20 | Eastman Kodak Company | Pourable particles of normally tacky plastic materials and process for their preparation |
JPH03121176A (en) * | 1989-10-04 | 1991-05-23 | Hirodain Kogyo Kk | Method for forming hot-melt self-adhesive |
FR2778631B1 (en) | 1998-05-14 | 2002-08-23 | Nordson Corp | PROCESS AND INSTALLATION FOR PACKAGING A STICKY PRODUCT AND SIMILAR PRODUCTS |
WO1992002348A1 (en) | 1990-08-01 | 1992-02-20 | H.B. Fuller Licensing And Financing Inc. | Method of packaging an adhesive composition and corresponding packaged article |
GB9114112D0 (en) * | 1991-06-29 | 1991-08-14 | Draper Neil | Packaging |
US5373682A (en) | 1992-05-18 | 1994-12-20 | National Starch And Chemical Investment Holding Corporation | Method for tackless packaging of hot melt adhesives |
JP2758270B2 (en) * | 1994-06-30 | 1998-05-28 | ナショナル スターチ アンド ケミカル インベストメント ホールディング コーポレイション | Method for coating hot melt adhesives |
FR2753714A1 (en) * | 1996-09-26 | 1998-03-27 | Henkel France | METHOD OF ANTI-ADHERENT TREATMENT OF A HOT-MELT SURFACE ADHESIVE |
US6006497A (en) * | 1997-03-26 | 1999-12-28 | Reichhold Chemicals, Inc. | Methods and apparatus for preparing a hot melt adhesive |
AU1073399A (en) * | 1997-10-08 | 1999-04-27 | H.B. Fuller Licensing And Financing Inc. | Hot melt adhesive pellet comprising continuous coating of pelletizing aid |
DE10030909A1 (en) | 1999-07-09 | 2001-03-01 | Henkel Kgaa | Hot-melt adhesive in granulate form use for adhesive bonding of substrates where the granulate is melted and then applied to the substrate, has compact outer shell |
DE10122437A1 (en) * | 2001-05-09 | 2002-11-28 | Henkel Kgaa | Hot melt adhesive in the form of granules |
US7350644B2 (en) * | 2002-10-21 | 2008-04-01 | National Starch And Chemical Investment Holding Corporation | Multi-layer film packaging of hot melt adhesive |
US7328547B2 (en) * | 2004-10-29 | 2008-02-12 | Bostik, Inc. | Process for packaging plastic materials like hot melt adhesives |
EP2415572A1 (en) * | 2010-08-04 | 2012-02-08 | Henkel AG & Co. KGaA | Free-flowing pressure sensitive adhesives |
JP2014512427A (en) * | 2011-03-17 | 2014-05-22 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | Coated PSA granules |
US9364985B2 (en) * | 2012-05-24 | 2016-06-14 | Henkel IP & Holding GmbH | Process for preparing flowable amorphous poly-alpha olefin adhesive pellets |
CN105264030B (en) * | 2013-05-29 | 2018-09-28 | H.B.富乐公司 | Package-type hot melt pressure sensitive adhesive |
JP6339977B2 (en) | 2015-07-15 | 2018-06-06 | 日本電信電話株式会社 | Video encoding apparatus and video encoding program |
-
2014
- 2014-06-12 ES ES14002028.0T patent/ES2614285T3/en active Active
- 2014-06-12 PL PL14002028T patent/PL2954995T3/en unknown
- 2014-06-12 PT PT140020280T patent/PT2954995T/en unknown
- 2014-06-12 EP EP14002028.0A patent/EP2954995B1/en active Active
- 2014-06-12 DK DK14002028.0T patent/DK2954995T3/en active
-
2015
- 2015-06-12 BR BR112016028868A patent/BR112016028868A2/en not_active Application Discontinuation
- 2015-06-12 WO PCT/EP2015/001193 patent/WO2015188947A1/en active Application Filing
- 2015-06-12 SG SG11201609895TA patent/SG11201609895TA/en unknown
- 2015-06-12 KR KR1020167034378A patent/KR102398442B1/en active IP Right Grant
- 2015-06-12 CN CN201580031455.2A patent/CN106459715B/en active Active
- 2015-06-12 RU RU2016151293A patent/RU2688853C2/en active
- 2015-06-12 US US15/317,736 patent/US10486190B2/en active Active
- 2015-06-12 CA CA2951740A patent/CA2951740A1/en not_active Abandoned
- 2015-06-12 JP JP2016572295A patent/JP7093157B2/en active Active
- 2015-06-12 AU AU2015273903A patent/AU2015273903A1/en not_active Abandoned
- 2015-06-12 MX MX2016015622A patent/MX2016015622A/en unknown
-
2016
- 2016-11-21 IL IL249097A patent/IL249097B/en active IP Right Grant
-
2020
- 2020-09-14 JP JP2020153493A patent/JP2021001347A/en active Pending
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