JPH0484960A - Absorptive articles - Google Patents
Absorptive articlesInfo
- Publication number
- JPH0484960A JPH0484960A JP2201624A JP20162490A JPH0484960A JP H0484960 A JPH0484960 A JP H0484960A JP 2201624 A JP2201624 A JP 2201624A JP 20162490 A JP20162490 A JP 20162490A JP H0484960 A JPH0484960 A JP H0484960A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- phase
- styrene
- softener
- permeable sheet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 67
- 230000001070 adhesive effect Effects 0.000 claims abstract description 62
- 239000000853 adhesive Substances 0.000 claims abstract description 60
- 229920001971 elastomer Polymers 0.000 claims abstract description 30
- 239000011347 resin Substances 0.000 claims abstract description 21
- 229920005989 resin Polymers 0.000 claims abstract description 21
- 229920000642 polymer Polymers 0.000 claims abstract description 16
- 230000004913 activation Effects 0.000 claims description 19
- 230000002745 absorbent Effects 0.000 claims description 16
- 239000002250 absorbent Substances 0.000 claims description 16
- 230000035699 permeability Effects 0.000 claims description 6
- 150000003440 styrenes Chemical class 0.000 claims description 5
- 230000000052 comparative effect Effects 0.000 abstract description 4
- 239000010734 process oil Substances 0.000 abstract description 3
- 229920006132 styrene block copolymer Polymers 0.000 abstract description 3
- 230000035515 penetration Effects 0.000 abstract 2
- BXOUVIIITJXIKB-UHFFFAOYSA-N ethene;styrene Chemical compound C=C.C=CC1=CC=CC=C1 BXOUVIIITJXIKB-UHFFFAOYSA-N 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 description 11
- 238000000576 coating method Methods 0.000 description 11
- 230000007423 decrease Effects 0.000 description 7
- 230000000740 bleeding effect Effects 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 230000008859 change Effects 0.000 description 5
- 239000004902 Softening Agent Substances 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- -1 styrene-ethylene-butylene-styrene Chemical class 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000005338 frosted glass Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- IORUEKDKNHHQAL-UHFFFAOYSA-N [2-tert-butyl-6-[(3-tert-butyl-2-hydroxy-5-methylphenyl)methyl]-4-methylphenyl] prop-2-enoate Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)OC(=O)C=C)=C1O IORUEKDKNHHQAL-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Absorbent Articles And Supports Therefor (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、吸収性物品に係り、詳しくは透湿シートを使
用した使い捨て紙おむつ等において、接着剤の組成成分
である軟化剤等がしみだす、いわゆる“裏抜は現象°′
が生じる程度が少ない吸収性物品に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to absorbent articles, and more specifically, in disposable disposable diapers and the like using a moisture-permeable sheet, a softening agent, etc., which is a component of an adhesive, seeps out. , so-called “back-cutting is a phenomenon°′
The present invention relates to an absorbent article in which the degree of occurrence of this phenomenon is small.
一般の使い捨て紙おむつは、肌に当接する側の液透過性
シートと衣服側の液不透過性シートとの間に吸収体を介
在させ、それらの所定部位を接着固定して構成されてい
る。A typical disposable diaper is constructed by interposing an absorbent body between a liquid-permeable sheet on the side that contacts the skin and a liquid-impermeable sheet on the clothing side, and fixing them at predetermined portions with adhesive.
而して、上記接着剤は、おむつ構成材料の接着性を向上
させ、またその塗工適性を向上させるために、ベースエ
ラストマーの割合を減らす一方、粘着付与剤及び軟化剤
の割合を増やした配合組成により、ベースエラストマー
のブロック構造を破壊して低粘度タイプにしたものが主
流になっている。Therefore, in order to improve the adhesion of the diaper constituent materials and its coating suitability, the above adhesive is formulated with a reduced proportion of the base elastomer and an increased proportion of the tackifier and softener. Depending on the composition, the mainstream is a low-viscosity type by destroying the block structure of the base elastomer.
また、上記液不透過性シートとしては、おむつの使用時
のむれ等を防止するために、通常、透湿シートが用いら
れている。Further, as the liquid-impermeable sheet, a moisture-permeable sheet is usually used in order to prevent stuffiness during use of the diaper.
しかし、透湿シートを用いた紙おむつに、低粘度タイプ
の接着剤を使用すると、接着剤の組成成分の一つである
軟化剤等が、接着剤中に保持されず、熱などの影響を受
けると、透湿シートの表面にしみ出す、いわゆる“裏抜
は現象”を生じる。However, when a low-viscosity adhesive is used for disposable diapers made with moisture-permeable sheets, the softener, which is one of the adhesive's components, is not retained in the adhesive and is susceptible to heat. This causes the so-called "bleed-out phenomenon" in which the moisture seeps out onto the surface of the moisture-permeable sheet.
このような“裏抜は現象”があると、透湿シートの表面
にべたつき感が生じたり、おむつの緒特性に悪影響が現
れたり、パック保持時におむつ同士のブッロキングが生
じたり、接着剤組成の変化により接着特性が経時変化し
たりする等、種々の不都合があった。If such a "lining-out phenomenon" occurs, the surface of the moisture-permeable sheet may feel sticky, the diaper's cord properties may be adversely affected, the diapers may block against each other when holding the pack, or the adhesive composition may There were various disadvantages such as changes in adhesive properties over time.
従って、本発明の目的は、接着剤中の組成成分である軟
化剤等のしみだし成分が透湿シートの表面にしみだす、
“裏抜は現象”が生じる程度が小さい吸収性物品を提供
することにある。Therefore, the object of the present invention is to prevent the seeping components such as softeners, which are compositional components in the adhesive, from seeping out onto the surface of the moisture permeable sheet.
The object of the present invention is to provide an absorbent article in which the "back-out phenomenon" occurs to a small degree.
本発明者等は、上記目的を達成すべく鋭意研究の結果、
透湿シートを用いた吸収性物品の接着剤として、スチレ
ン系ブロックポリマー、粘着付与剤樹脂及び軟化剤を主
成分とし、スチレン相とゴム相との2相ブロック構造を
保持しているものを使用すると、接着性及び塗工性等を
保持しつつ、透湿シートの表面に接着剤の組成成分であ
る軟化剤等がしみだす“裏抜は現象”を生じる程度が小
さいことを知見した。As a result of intensive research to achieve the above purpose, the present inventors have found that
As an adhesive for absorbent articles using moisture-permeable sheets, we use an adhesive whose main components are a styrene block polymer, a tackifier resin, and a softener, and which maintains a two-phase block structure of a styrene phase and a rubber phase. As a result, it was found that while maintaining adhesion and coatability, the degree of occurrence of the "bleed-out phenomenon" in which the softening agent, etc., which is a component of the adhesive, seeps onto the surface of the moisture permeable sheet is small.
本発明は上記知見に基づきなされたもので、接着剤が塗
布された透湿シートを備えた吸収性物品において、上記
透湿シートが、透湿量0.7 g / 100crJ・
h 〜2.8 g/ 100cd・hの透湿シートで、
上記接着剤が、スチレン系ブロックポリマー粘着付与剤
樹脂及び軟化剤を主成分とし、スチレン相とゴム相との
2相ブロック構造を保持している接着剤であることを特
徴とする吸収性物品を提供するものである。The present invention has been made based on the above findings, and provides an absorbent article including a moisture permeable sheet coated with an adhesive, wherein the moisture permeable sheet has a moisture permeability of 0.7 g/100 crJ.
h ~2.8 g/100 cd・h moisture permeable sheet,
The absorbent article is characterized in that the adhesive contains a styrene block polymer tackifier resin and a softener as main components and maintains a two-phase block structure of a styrene phase and a rubber phase. This is what we provide.
以下、本発明の吸収性物品について詳述する。The absorbent article of the present invention will be described in detail below.
本発明に用いられる透湿シートは、透湿量が、0.7
g/ 100ci−h〜2.8 g/ 100ca−h
のものである。このような透湿シートを、使い捨ておむ
つの液不透過性シート等として使用すると、おむつの使
用時におけるむれ等を防止することができる。The moisture permeable sheet used in the present invention has a moisture permeability of 0.7
g/100ci-h~2.8 g/100ca-h
belongs to. When such a moisture-permeable sheet is used as a liquid-impermeable sheet of a disposable diaper, it is possible to prevent stuffiness during use of the diaper.
而して、本発明においては、接着剤として、スチレン系
ブロックポリマー、粘着付与剤樹脂及び軟化剤を主成分
とし、スチレン相とゴム相との2相ブロック構造を保持
しているものが用いられる。Therefore, in the present invention, the adhesive used is one that contains a styrene block polymer, a tackifier resin, and a softener as main components and maintains a two-phase block structure of a styrene phase and a rubber phase. .
上記接着剤のスチレン系ブロックポリマーとしては、ス
チレン−エチレン−ブチレン−スチレンブロック共重合
体(SEBS)、スチレン−イソプレン−スチレンブロ
ック共重合体(S I S)、スチレン−ブタジェン−
スチレンブロック共重合体(SBS)、スチレン−エチ
レン−プロピレン−スチレンブロック共重合体(SEP
S)等がある。これらのスチレン系ブロックポリマーは
、スチレン部分の分子量が7000〜20000、ゴム
部分の分子量が35000〜70000のブロック共重
合体である。Examples of the styrene block polymer of the adhesive include styrene-ethylene-butylene-styrene block copolymer (SEBS), styrene-isoprene-styrene block copolymer (SI S), styrene-butadiene-
Styrene block copolymer (SBS), styrene-ethylene-propylene-styrene block copolymer (SEP)
S) etc. These styrenic block polymers are block copolymers in which the styrene portion has a molecular weight of 7,000 to 20,000 and the rubber portion has a molecular weight of 35,000 to 70,000.
また、上記粘着付与樹脂としては、軟化点が80°C以
上で、分子量が400〜2000であるC1系石油樹脂
、C1系石油樹脂、Cs / Cq系石油樹脂、αピネ
ン又はβピネン又はジペンテンの重合体であるポリテル
ペン樹脂、ロジン系樹脂、及びこれらの水添物等がある
−0
また、上記軟化剤としては、軟化点が10℃以下で平均
分子量が200〜700のプロセスオイル、各種可塑剤
、ポリブテン、液状樹脂等がある。The tackifying resin may include C1 petroleum resins, C1 petroleum resins, Cs/Cq petroleum resins, α-pinene, β-pinene, or dipentene, which have a softening point of 80°C or higher and a molecular weight of 400 to 2000. There are polymers such as polyterpene resins, rosin resins, and hydrogenated products thereof.In addition, the softening agents include process oils with a softening point of 10°C or less and an average molecular weight of 200 to 700, and various plasticizers. , polybutene, liquid resin, etc.
上記の2相ブロック構造又はそれに近似した構造を保持
する上で好ましい接着剤は、スチレン系ブロックポリマ
ー100重量部に対し、粘着付与剤樹脂を150〜20
0重量部、好ましくは160〜180重量部にし、また
軟化剤を30〜100重量部、好ましくは40〜70重
量部に設定したものである。このような組成の接着剤は
、上記軟化剤の占める割合が、大体lO%〜25%程度
になるものである。A preferable adhesive for maintaining the above two-phase block structure or a structure similar to it contains 150 to 20 parts by weight of tackifier resin per 100 parts by weight of the styrenic block polymer.
0 parts by weight, preferably 160 to 180 parts by weight, and the softener is set to 30 to 100 parts by weight, preferably 40 to 70 parts by weight. In an adhesive having such a composition, the proportion of the softening agent is approximately 10% to 25%.
ここで、上記粘着付与樹脂が150重量部よりも少なく
、また軟化剤が30重量部よりも少なくなると(上記軟
化剤の占める割合を10%よりも少なくなると)、タッ
ク性及び粘着力が低くなり、また粘度上昇により塗工性
低下が悪くなり、好ましくない。Here, if the tackifier resin is less than 150 parts by weight and the softener is less than 30 parts by weight (the proportion of the softener is less than 10%), the tackiness and adhesive strength will decrease. Moreover, the increase in viscosity deteriorates the coating properties, which is not preferable.
また、上記粘着付与樹脂が200重量部よりも多く、ま
た軟化剤を100重量部よりも多いと(上記軟化剤の占
める割合が25%を趙えると)、2相ブロック構造が破
壊されるおそれがある。Furthermore, if the tackifying resin exceeds 200 parts by weight and the softener exceeds 100 parts by weight (if the proportion of the softener exceeds 25%), the two-phase block structure may be destroyed. There is.
上記接着剤には、スチレン系ブロックポリマー粘着付与
樹脂及び軟化剤の他に、酸化防止剤を添加するのが好ま
しい。この場合、酸化防止剤は、上記スチレン系ブロッ
クポリマー100重量部に対して1〜3重量部添加する
のが好ましい。この酸化防止剤としては、例えばイルガ
ノックス1゜10(チバガイギ銖製の商品名)、イルガ
ノックス1076 (チバガイギ株製の商品名)又はス
ミライザGM(住人化学■の商品名)等が用いられる。In addition to the styrenic block polymer tackifier resin and softener, an antioxidant is preferably added to the adhesive. In this case, the antioxidant is preferably added in an amount of 1 to 3 parts by weight per 100 parts by weight of the styrene block polymer. As the antioxidant, for example, Irganox 1°10 (trade name, manufactured by Ciba Gaigi Co., Ltd.), Irganox 1076 (trade name, manufactured by Ciba Gaigi Co., Ltd.), or Sumilizer GM (trade name, manufactured by Susumu Kagaku 2), etc. can be used.
上記接着剤は、180°C以下の温度でホットメルトに
より塗工することもできるため、使い捨ておむフ等の吸
収性物品の生産に適している。The above adhesive can also be applied by hot melting at a temperature of 180° C. or lower, and is therefore suitable for producing absorbent articles such as disposable diapers.
本発明の吸収性物品は、上述した透湿量0.7g/ 1
00c+fl−h〜2.8 g/ 100c+Il−h
(7)透湿シートを使用し、この透湿シートに塗布する
接着剤として上記接着剤を使用したもので、例えば使い
捨ておむつや住理用品等に通用することができる。The absorbent article of the present invention has the above-mentioned moisture permeability of 0.7 g/1
00c+fl-h~2.8 g/100c+Il-h
(7) A moisture-permeable sheet is used, and the adhesive described above is used as the adhesive applied to the moisture-permeable sheet, and can be used, for example, in disposable diapers, household goods, etc.
本発明の吸収性物品において、“裏抜は現象”を生じる
程度が小さくなるのは、前述した接着剤を用いることに
よるものである。そして、その詳細な理由は明らがでは
ないが、次のように考えられる。In the absorbent article of the present invention, the degree of occurrence of the "bleed-out phenomenon" is reduced by using the above-mentioned adhesive. Although the detailed reason is not clear, it is thought to be as follows.
本発明で用いられる、スチレン相とゴム相との2相ブロ
ック構造を保持している接着剤の構造は、図解して説明
すると、第1図の概念図に示すように、スチレンドメイ
ン1とゴム相2とが存在し、また第2図のグラフに示す
ように、スチレン相緩和ピークとゴム相緩和ピークとの
2つのピークが存在しているものと認められる。The structure of the adhesive used in the present invention, which maintains a two-phase block structure of a styrene phase and a rubber phase, can be explained diagrammatically as shown in the conceptual diagram of FIG. As shown in the graph of FIG. 2, it is recognized that there are two peaks: a styrene phase relaxation peak and a rubber phase relaxation peak.
なお、第2図は、動的粘弾性測定法により上記接着剤の
動的粘弾性の挙動を測定して、温度分散に対する損失弾
性率E′及びtanδ(tanδ−損失弾性率E″/貯
藏弾性率E’ )を求めたグラフで、横軸に温度(°C
)を表し、縦軸にtanδを表している。FIG. 2 shows the behavior of the dynamic viscoelasticity of the adhesive measured by the dynamic viscoelasticity measurement method, and the loss modulus E' and tan δ (tan δ - loss modulus E''/storage elasticity The graph shows the temperature (°C) on the horizontal axis.
), and the vertical axis represents tan δ.
而して、上記接着剤においては、スチレンドメインによ
ってゴム相の運動が束縛され、その結果、ゴム相分子鎖
の絡み合いが住じ、このゴム相分子鎖の絡み合いの中に
、しみだし成分である軟化剤や低分子量ポリマー成分等
が閉じ込められてしまい、゛裏抜は現象”が防止される
ものと、考えられる。Therefore, in the above adhesive, the movement of the rubber phase is restrained by the styrene domain, and as a result, the entanglement of the rubber phase molecular chains resides, and the seeping component is present in the entanglement of the rubber phase molecular chains. It is thought that the softener, low molecular weight polymer components, etc. are trapped, and the "bleed-out phenomenon" is prevented.
因みに、上記軟化剤を100重量部よりも多くし、例え
ば上記接着剤中に上記軟化剤が占める割合を30%程度
にすると、第2図に示す2つのピークの間に中間の性質
を示す第3の緩和ピークがみられるようになる。このよ
うなもの(3相構造をとるもの)においては、スチレン
ドメインが減少し、この結果、ゴム相分子鎖の絡み合い
が減少し、可塑化されたスチレンドメインがゴム相に相
溶し、中間の性質を示す相が生じ、その結果、しみだし
成分を閉じ込めて保持する能力が低下し、“裏抜は現象
゛が生じるものと考えられる。Incidentally, if the amount of the softener is increased to more than 100 parts by weight, for example, if the proportion of the softener in the adhesive is about 30%, a peak with properties intermediate between the two peaks shown in FIG. 2 will be produced. 3 relaxation peak becomes visible. In such products (those with a three-phase structure), the styrene domains are reduced, and as a result, the entanglement of the rubber phase molecular chains is reduced, and the plasticized styrene domains are compatible with the rubber phase, and the intermediate It is thought that a phase exhibiting properties is formed, and as a result, the ability to trap and retain exuded components is reduced, resulting in the "bleed-out phenomenon."
また、上記軟化剤を更に多くし、例えば上記接着剤中に
上記軟化剤が占める割合を40%程度にすると、ドメイ
ン構造がゴム相に完全に相溶し、2つの緩和ピークが1
つになると考えられる。この場合には、しみだし成分を
閉じ込めて保持する能力がほぼ消失し、これによって“
裏抜は現象”が更に促進するものと考えられる。Furthermore, when the amount of the softener is further increased, for example, the proportion of the softener in the adhesive becomes about 40%, the domain structure becomes completely compatible with the rubber phase, and the two relaxation peaks become 1.
It is thought that there will be two. In this case, the ability to trap and retain the exuding components is almost completely lost, and this results in “
It is thought that the phenomenon of "back-cutting" is further promoted.
また、上記の2相ブロック構造を構成する、上記スチレ
ン相及び上記ゴム相の、それぞれの見掛けの活性化エネ
ルギーを、周波数分散により求めてみると、上記スチレ
ン相の見掛けの活性化エネルギーは50Kcal/mo
l以上で、また上記ゴム相の見掛けの活性化工ふルギー
は35Kcal/mol 以上となる。Further, when the apparent activation energies of the styrene phase and the rubber phase, which constitute the two-phase block structure, are determined by frequency dispersion, the apparent activation energy of the styrene phase is 50 Kcal/ mo
1 or more, and the apparent activated fuel of the rubber phase is 35 Kcal/mol or more.
このように、スチレン相の見掛けの活性化エネルギーが
50 Kcal/n+o1以上と大きく、ゴム相の見掛
けの活性化エネルギーが35にcal/mol以上と大
きい接着剤は、それだけ分子運動を引き起こすのに必要
なエネルギーを多く必要とするために、外部から熱が与
えられても、しみだし成分を接着剤中に保持しておくこ
とができるため、パ裏抜げ現象”が小さくなるものと考
えられる。In this way, an adhesive in which the styrene phase has a large apparent activation energy of 50 Kcal/n+o1 or more, and the rubber phase has a large apparent activation energy of 35 Kcal/mol or more, has a large amount of energy required to cause molecular movement. Since the adhesive requires a lot of energy, even if heat is applied from the outside, the seeping components can be retained in the adhesive, which is thought to reduce the phenomenon of lining-out.
なお、上記°“裏抜は現象゛は、透湿シートに接着剤を
塗布したとき、軟化剤等のしみだし成分が、透湿シート
の表面を濡らして裏抜けした(しみだした)ようになる
現象であり、曇りガラスを水で濡らすと、光が透過し、
曇りガラスを介して外側が見えるようになる現象と同じ
である。In addition, the above-mentioned "bleed-out" phenomenon occurs when adhesive is applied to a moisture-permeable sheet, and components such as softeners wet the surface of the moisture-permeable sheet and bleed through (bleed through). This is a phenomenon that occurs when frosted glass is wetted with water, allowing light to pass through it.
This is the same phenomenon as being able to see outside through frosted glass.
本発明者等は、このような現象を利用して上記“′裏抜
は現象”を定量化することを試みた。即ち、第3図に示
すように、透湿シートに接着剤を塗布したサンプル3の
背面に、黒色プレート4を配置し、上記サンプル3の表
面に、透明ガラス板5を配置し、上記サンプル3の表面
側から波長459nmの青色入射光を照射する一方、上
記サンプル3からの反射光の反射率を測定することによ
り、裏抜けの程度(しみだしの程度)の定量化を試みた
。The present inventors attempted to quantify the above-mentioned "back-out phenomenon" by utilizing such a phenomenon. That is, as shown in FIG. 3, a black plate 4 is placed on the back side of a sample 3 made of a moisture-permeable sheet coated with adhesive, a transparent glass plate 5 is placed on the surface of the sample 3, and the sample 3 An attempt was made to quantify the degree of strike-through (extent of seepage) by measuring the reflectance of the reflected light from Sample 3 while irradiating blue incident light with a wavelength of 459 nm from the surface side of the sample.
この方法によれば、裏抜けの程度が大きいと(しみだし
の程度が大きいと)、青色入射光がサンプル3を透過し
て黒色プレート4に至り、該黒色プレート4に吸収され
て、上記サンプル3からの反射光の反射率が低下し、ま
た、裏抜けの程度が小さいと(しみだしの程度が小さい
と)、青色入射光がサンプル3を透過して黒色プレート
4に至ることが少なく、該黒色プレート4に吸収されず
にサンプル3で反射し、上記サンプル3からの反射光の
反射率が高くなる。According to this method, when the degree of bleed through is large (the degree of seepage is large), the incident blue light passes through the sample 3 and reaches the black plate 4, and is absorbed by the black plate 4. If the reflectance of the reflected light from the sample 3 decreases, and if the degree of bleed-through is small (the degree of seepage is small), the incident blue light will be less likely to pass through the sample 3 and reach the black plate 4. The light is reflected by the sample 3 without being absorbed by the black plate 4, and the reflectance of the light reflected from the sample 3 increases.
本発明の吸収性物品によれば、透湿量0.7g/100
c+fl−h〜2.8g/100cIil−hの透湿シ
ートを使用し、この透湿シートに塗布する接着剤として
、スチレン系ブロックポリマー、粘着付与剤樹脂及び軟
化剤を主成分とし、スチレン相とゴム相との2相ブロッ
ク構造を保持しているものを使用したので、温度上昇に
より分子運動が大きくなっても、接着剤の組成成分であ
る軟化剤等を、接着剤中に保持することができ、透湿シ
ートの表面にしみでる“裏抜は現象”が生じない。According to the absorbent article of the present invention, the moisture permeability is 0.7 g/100
A moisture-permeable sheet with a weight of c+fl-h to 2.8 g/100 cIil-h is used, and the adhesive applied to this moisture-permeable sheet contains a styrene block polymer, a tackifier resin, and a softener as main components, and the styrene phase and Since we used a material that maintains a two-phase block structure with the rubber phase, even if molecular motion increases due to temperature rise, the softener, etc., which is a component of the adhesive, can be retained in the adhesive. This eliminates the ``bleed-out phenomenon'' that occurs on the surface of the moisture-permeable sheet.
このため、透湿シートの表面にべたつき感が生じたり、
おむつの緒特性に悪影響が現れたり、パック保存時にお
むつ同士のブロッキングが生じたり、接着剤組成の変化
により接着特性が経時変化したすする等の不都合がない
。For this reason, the surface of the moisture permeable sheet may feel sticky,
There is no adverse effect on the diaper strap properties, there is no blocking between the diapers during pack storage, there is no problem such as sluggishness due to changes in the adhesive properties over time due to changes in the adhesive composition.
以下、本発明の詳細な説明する。 The present invention will be explained in detail below.
まず、スチレン系ブロックポリマーとして5EBS(ス
チレン−エチレン−ブチレン−スチレンプロッタ共重合
体)、粘着付与樹脂としてC1系石油樹脂、軟化剤とし
てナフテン系プロセスオイルを用い、更に酸化防止剤と
してチバガイギ社製のイルガノックス1010rペンタ
エリスリチル−テトラキス(3−(3,5−ジ−t−ブ
チル−4−ヒドロキシフェニル)プロピオネート〕」ヲ
用い、温度160°C1時間40分の条件の下で、ニー
ダ−により混練して、以下の表−1に示す各種重量比の
接着剤を調製した。First, 5EBS (styrene-ethylene-butylene-styrene plotter copolymer) was used as the styrene block polymer, C1 petroleum resin was used as the tackifying resin, naphthene process oil was used as the softener, and Ciba-Geigi's 5EBS (styrene-ethylene-butylene-styrene plotter copolymer) was used as the styrene block polymer. Using Irganox 1010r pentaerythrityl-tetrakis (3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate), it was kneaded in a kneader at a temperature of 160°C for 1 hour and 40 minutes. Adhesives having various weight ratios shown in Table 1 below were prepared.
なお、酸化防止剤の配合量は、全ての接着剤で同じにし
、5EBSに対して3重量%にした。The amount of antioxidant added was the same for all adhesives, and was 3% by weight based on 5EBS.
次いで、上記接着剤を、温度160°Cでホットメルト
により、剥離紙上に厚さ40±5μになるようにベタ塗
工した後、透湿量1.7 g/ 100c+ll・hの
透湿シートに転写塗工し、この透湿シートを用いて使い
捨ておむつを製作した。そして、上記使い捨ておむつを
温度60″Cで10日間保存した後、しみだしめ有無を
目視により観察したところ、以下の表−1に示す結果が
得られた。Next, the above adhesive was applied by hot melting at a temperature of 160°C onto a release paper to a thickness of 40±5μ, and then formed into a moisture permeable sheet with a moisture permeability of 1.7 g/100c+ll・h. Transfer coating was performed, and a disposable diaper was manufactured using this moisture permeable sheet. After storing the above disposable diaper at a temperature of 60''C for 10 days, the presence or absence of seepage was visually observed, and the results shown in Table 1 below were obtained.
なお、表−1中、記号○はしみだしが殆ど生じなかった
ことを示し、また記号Δはしみたしが多少化じたことを
示し、記号×はじみだしが大きく生じたことを示す。In Table 1, the symbol ◯ indicates that almost no oozing occurred, the symbol Δ indicates that the oozing has changed to some extent, and the symbol × indicates that oozing occurred to a large extent.
また、しみだしの程度を定量的に測定するために、上記
使い捨ておむつに用いたものと同じ透湿シートを第3図
に示す黒色パネル4に相当する台紙に貼りつけ、測定試
料を作成した。そして、上記測定試料を温度60°Cで
10日間保存した後に反射率を測定し、またこの反射率
に基づいて低下率を算出し、これらを表−1に併記した
。In addition, in order to quantitatively measure the degree of seepage, a measurement sample was prepared by pasting the same moisture-permeable sheet as that used in the disposable diaper on a mount corresponding to the black panel 4 shown in FIG. 3. Then, the reflectance was measured after storing the measurement sample at a temperature of 60° C. for 10 days, and the reduction rate was calculated based on this reflectance, and these are also listed in Table-1.
なお、反射率は色差計(日本電気工業社製)を用いて測
定した。また、反射率の低下率は、次式により算出した
。Note that the reflectance was measured using a color difference meter (manufactured by NEC Corporation). Further, the rate of decrease in reflectance was calculated using the following formula.
反射率の低下率=(a−b)/a
1−(a/b)(%〕
aニブランクの反射率
b;10日間経過した後の反射率
更に、本発明品NO,1,2、比較品No、 1.2に
使用した接着剤の相構造及び見掛けの活性化エネルギー
も表−1に併記した。Reduction rate of reflectance = (a-b)/a 1-(a/b) (%) a Reflectance of blank b; Reflectance after 10 days Furthermore, present invention products NO, 1, 2, comparison The phase structure and apparent activation energy of the adhesive used in Product No. 1.2 are also listed in Table 1.
ここで、相構造は、動的粘弾性測定法により求めた。即
ち、まず上記接着剤を溶融し、線径0.5晒、巻径5M
、長さ6ffI[11のコイルスプリング(晶相発条製
作所製)にそれぞれ含浸させた。次いで、レオパイブロ
ン(東洋ボールドウィンDDV−II−BP)を用い、
周波数3.5 Hzで、上記コイルスプリングの貯蔵弾
性率E゛、損失弾性率E”及び損失正接tanδ(ta
nδ−E″/E゛)を測定した。このとき、温度範囲は
一200°C〜+120°Cとした。また昇温速度は3
”I: /winとし、冷媒は液体窒素を使用した。Here, the phase structure was determined by dynamic viscoelasticity measurement. That is, first, the above adhesive is melted, the wire diameter is 0.5, and the winding diameter is 5M.
, a length of 6ffI [11] coil springs (manufactured by Seisou Hatsujo Seisakusho) were each impregnated with the solution. Next, using Reopybron (Toyo Baldwin DDV-II-BP),
At a frequency of 3.5 Hz, the storage elastic modulus E'', loss elastic modulus E'', and loss tangent tan δ (ta
nδ-E''/E゛) was measured. At this time, the temperature range was -200°C to +120°C. Also, the heating rate was 3
”I: /win, and liquid nitrogen was used as the refrigerant.
また、見掛けの活性化エネルギーは、上記動的粘弾性測
定の中で、周波数を3.5 Hz、11Hz、35Hz
、110Hzと変化させて求めた。即ち、まず、各々の
周波数でのスチレン相、ゴム相及び均一相に対応する各
janδ分散ピーク温度を測定し、次いでこの測定結果
に基づいて下記に示すアレニウスの式を用い、lnfと
一1/Tとの関係を表すグラフを求め、この後、グラフ
に示す直線の傾きからスチレン相、ゴム相及び均一相の
見掛けの活性化エネルギーを求めた。In addition, the apparent activation energy is determined by changing the frequency to 3.5 Hz, 11 Hz, and 35 Hz in the above dynamic viscoelasticity measurement.
, 110Hz. That is, first, each jan δ dispersion peak temperature corresponding to the styrene phase, rubber phase, and homogeneous phase at each frequency is measured, and then, based on the measurement results, using the Arrhenius equation shown below, lnf and -1/ A graph representing the relationship with T was obtained, and then, the apparent activation energy of the styrene phase, rubber phase, and homogeneous phase was obtained from the slope of the straight line shown in the graph.
アレニウスの式
%式%
E ;見掛けの活性化エネルギー
(cal / mol)
R;ガス定数
T ;分散ピーク温度じK)
なお、表−1中、Stはスチレン相の見掛けの活性化エ
ネルギー、Gはゴム相の見掛けの活性比表−1
上記表−1から明らかな如く、本発明品No、 1は目
視による観察でしみたしが殆どみられず、またしみだし
の程度を定量化する反射率も66%と高く、“裏抜は現
象゛は殆ど生じないことが確認さレタ。また、反射率の
低下率も8%も少なく、経時変化が殆ど生じないことが
確認された。Arrhenius formula % formula % E; apparent activation energy (cal/mol) R; gas constant T; dispersion peak temperature (K) In Table 1, St is the apparent activation energy of the styrene phase, and G is the apparent activation energy of the styrene phase. Apparent activity ratio table of rubber phase-1 As is clear from Table-1 above, inventive product No. 1 shows almost no staining when visually observed, and has a reflectance that quantifies the degree of staining. The rate of decrease in reflectance was as high as 66%, confirming that almost no phenomenon occurred during back-extraction.Also, the rate of decrease in reflectance was as low as 8%, confirming that almost no change over time occurred.
また、使用した接着剤の相構造は2相ブロック構造であ
ることが確認された。また、スチレン相の見掛けの活性
化エネルギーは75.9 cal/mol、ゴム相の見
掛けの活性化エネルギーは39.0 cal/molで
あった。Furthermore, it was confirmed that the phase structure of the adhesive used was a two-phase block structure. Further, the apparent activation energy of the styrene phase was 75.9 cal/mol, and the apparent activation energy of the rubber phase was 39.0 cal/mol.
また、本発明品階2も上記本発明品No、1とほぼ同様
の結果(反射率65%、反射率の低下率10%)が得ら
れた。In addition, almost the same results as the invention product No. 1 (reflectance 65%, reflectance reduction rate 10%) were obtained for the invention product No. 2.
また、使用した接着剤の相構造は2相ブロック構造であ
ることが確認された。また、スチレン相の見掛けの活性
化エネルギーは51.2 cal/mol、ゴム相の見
掛けの活性化エネルギーは36.5 cal/molで
あった。Furthermore, it was confirmed that the phase structure of the adhesive used was a two-phase block structure. Further, the apparent activation energy of the styrene phase was 51.2 cal/mol, and the apparent activation energy of the rubber phase was 36.5 cal/mol.
これに対し、比較品階1は、目視による観察でじみだし
が多少みられ、またしみだしの程度を定量化する反射率
も57%と低く、“裏抜は現象′”が生した。また、反
射率の低下率は21%と高く、経時変化が大きく生じた
。On the other hand, the comparison product Grade 1 showed some bleeding when visually observed, and the reflectance, which quantifies the degree of bleeding, was as low as 57%, resulting in the "bleed-through phenomenon." Further, the rate of decrease in reflectance was as high as 21%, and there was a large change over time.
また、使用した接着剤の相構造は3相構造であった。ま
た、スチレン相の見掛けの活性化エネルギーは45.0
cal/+molで、50.0 cal/molより
も低く、ゴム相の見掛けの活性化エネルギーは31゜5
cal/mol で、35.0 cal/solよりも
低かった。Further, the phase structure of the adhesive used was a three-phase structure. Also, the apparent activation energy of the styrene phase is 45.0
cal/+mol, lower than 50.0 cal/mol, and the apparent activation energy of the rubber phase is 31°5
cal/mol, which was lower than 35.0 cal/sol.
また、比較品Nα2は、目視による観察でしみだしが大
きくみられ、じみだしの程度を定量化する反射率も52
%と更に低く、“裏抜は現象”が大きく生じた。また、
反射率の低下率は28%と更に高く、経時変化が大きく
生じた。In addition, the comparison product Nα2 has a large amount of seepage when visually observed, and the reflectance, which is used to quantify the degree of seepage, is 52.
%, and the "bleed-out phenomenon" occurred significantly. Also,
The rate of decrease in reflectance was even higher at 28%, and a large change over time occurred.
また、接着剤の相構造は、スチレンドメインがゴム相に
完全相溶し、均一相になった。また、見掛けの活性化エ
ネルギーは30.0 cal/molで、上記試料Nα
3の場合よりも更に低くなった。Furthermore, the phase structure of the adhesive was such that the styrene domain was completely compatible with the rubber phase, resulting in a homogeneous phase. In addition, the apparent activation energy is 30.0 cal/mol, and the above sample Nα
It was even lower than in case 3.
また、本発明品Nα1.2、比較品Nα1.2に使用し
た接着剤を、温度160°でホットメルトにより、剥離
紙上に5g/mlでスパイラル塗工及び0.07g/本
・mでビード塗工した。そして、上記剥離紙を台紙上に
貼りつけて、しみたしの経時変化を目視で判断する試料
を作成した。この試料を温度60°のもとて10日間保
存した後、しみだしの経時変化を目視で判断したところ
、以下の表−2に示す結果が得られた。In addition, the adhesives used for the inventive product Nα1.2 and the comparative product Nα1.2 were applied by hot melting at a temperature of 160° onto release paper at 5 g/ml in a spiral coating and at 0.07 g/piece/m in a bead coating. I worked on it. Then, the above-mentioned release paper was pasted onto a mount to prepare a sample for visually determining the change in stain over time. After this sample was stored at a temperature of 60° for 10 days, the change in exudation over time was visually judged, and the results shown in Table 2 below were obtained.
なお、表−2中、記号Oはしみだしが殆ど生じなかった
ことを示し、またΔはしみたしが多少生じたことを示し
、また×はしみだしが大きく生じたことを示す。In Table 2, the symbol O indicates that almost no bleeding occurred, Δ indicates that some bleeding occurred, and × indicates that a large amount of bleeding occurred.
上記表−2から明らかな如く、本発明品Nα1.2の接
着剤では、スパイラル塗工、ビード塗工しても、いずれ
の場合も、“裏抜は現象”が殆ど生じないことが確認さ
れた。As is clear from Table 2 above, with the adhesive of the present invention Nα1.2, it has been confirmed that the "back-out phenomenon" hardly occurs in both spiral coating and bead coating. Ta.
これに対し、比較品阻3の接着剤では、スパイラル塗工
、ビード塗工すると、いずれの場合も“°裏抜は現象”
が多少生じた。また、比較品に2の接着剤では、スパイ
ラル塗工、ビード塗工すると、いずれの場合も“裏抜は
現象”が大きく生じた。On the other hand, with the comparative adhesive No. 3, when spiral coating and bead coating are applied, "° back-out is a phenomenon" in both cases.
occurred to some extent. In addition, with the comparative adhesive No. 2, when spiral coating and bead coating were applied, the "bleed-out phenomenon" occurred significantly in both cases.
本発明の吸収製物品は、接着剤中の組成成分である軟化
剤等のしみだし成分が透湿シートの表面にしみだす“裏
抜は現象”が生じる程度が小さい。In the absorbent article of the present invention, the "bleed-out phenomenon" in which seeping components such as softeners, which are constituents in the adhesive, seep out onto the surface of the moisture permeable sheet is small.
【図面の簡単な説明】
第1図は接着剤の相構造を概念的に表した概念図、第2
図は動的粘性弾性測定法により接着剤の動的粘性弾性の
挙動を測定して求めたグラフであって、温度分散に対す
るtanδ(tanδ=損失弾性率E”/貯蔵弾性率E
’ )を示すグラフ、第3図は“裏抜は現象”の程度の
測定原理を示す測定原理説明図である。
l;スチレン相 2;ゴム相
3;サンプル 4;黒色プレート5;透明ガ
ラス板[Brief explanation of the drawings] Figure 1 is a conceptual diagram conceptually representing the phase structure of adhesives;
The figure is a graph obtained by measuring the behavior of dynamic viscoelasticity of an adhesive using a dynamic viscoelasticity measurement method, and shows tanδ (tanδ=loss modulus E''/storage modulus E) with respect to temperature dispersion.
Figure 3 is an explanatory diagram of the measurement principle showing the degree of "bleeding out is a phenomenon". l; Styrene phase 2; Rubber phase 3; Sample 4; Black plate 5; Transparent glass plate
Claims (2)
品において、 上記透湿シートが、透湿量0.7g/100cm^2・
h〜2.8g/100cm^2・hの透湿シートで、上
記接着剤が、スチレン系ブロックポリマー、粘着付与剤
樹脂及び軟化剤を主成分とし、スチレン相とゴム相との
2相ブロック構造を保持している接着剤であることを特
徴とする吸収性物品。(1) In an absorbent article equipped with a moisture permeable sheet coated with an adhesive, the moisture permeable sheet has a moisture permeability of 0.7 g/100 cm^2.
h~2.8g/100cm^2・h moisture permeable sheet, the adhesive has a styrene block polymer, tackifier resin, and softener as main components, and has a two-phase block structure of a styrene phase and a rubber phase. An absorbent article characterized by being an adhesive that retains.
0Kcal/mol以上で、また上記ゴム相の見掛けの
活性化エネルギーが35Kcal/mol以上であるこ
とを特徴とする請求項(1)記載の吸収性物品。(2) The apparent activation energy of the above styrene phase is 5
0 Kcal/mol or more, and the absorbent article according to claim 1, wherein the apparent activation energy of the rubber phase is 35 Kcal/mol or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2201624A JP3029853B2 (en) | 1990-07-30 | 1990-07-30 | Absorbent articles |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2201624A JP3029853B2 (en) | 1990-07-30 | 1990-07-30 | Absorbent articles |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0484960A true JPH0484960A (en) | 1992-03-18 |
JP3029853B2 JP3029853B2 (en) | 2000-04-10 |
Family
ID=16444152
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2201624A Expired - Lifetime JP3029853B2 (en) | 1990-07-30 | 1990-07-30 | Absorbent articles |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3029853B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5738669A (en) * | 1994-04-12 | 1998-04-14 | Kao Corporation | Absorbent article |
EP0993832A1 (en) * | 1998-10-16 | 2000-04-19 | The Procter & Gamble Company | Absorbent article comprising a microporous film with an adhesive layer |
-
1990
- 1990-07-30 JP JP2201624A patent/JP3029853B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5738669A (en) * | 1994-04-12 | 1998-04-14 | Kao Corporation | Absorbent article |
EP0993832A1 (en) * | 1998-10-16 | 2000-04-19 | The Procter & Gamble Company | Absorbent article comprising a microporous film with an adhesive layer |
WO2000023122A1 (en) * | 1998-10-16 | 2000-04-27 | The Procter & Gamble Company | Absorbent article with microporous film and adhesive |
Also Published As
Publication number | Publication date |
---|---|
JP3029853B2 (en) | 2000-04-10 |
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