JP2013208410A5 - - Google Patents
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- JP2013208410A5 JP2013208410A5 JP2012082514A JP2012082514A JP2013208410A5 JP 2013208410 A5 JP2013208410 A5 JP 2013208410A5 JP 2012082514 A JP2012082514 A JP 2012082514A JP 2012082514 A JP2012082514 A JP 2012082514A JP 2013208410 A5 JP2013208410 A5 JP 2013208410A5
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- JP
- Japan
- Prior art keywords
- chain hydrocarbon
- group
- hydrocarbon moiety
- absorbent article
- bond
- 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.)
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- 210000004369 Blood Anatomy 0.000 claims description 11
- 239000008280 blood Substances 0.000 claims description 11
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 24
- -1 polyoxy Polymers 0.000 claims 24
- 239000004215 Carbon black (E152) Substances 0.000 claims 17
- 230000002745 absorbent Effects 0.000 claims 16
- 239000002250 absorbent Substances 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 12
- 239000007788 liquid Substances 0.000 claims 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 11
- 150000002148 esters Chemical class 0.000 claims 10
- 125000001931 aliphatic group Chemical group 0.000 claims 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 8
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 8
- 150000002430 hydrocarbons Chemical class 0.000 claims 7
- 239000003795 chemical substances by application Substances 0.000 claims 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims 5
- 239000000194 fatty acid Substances 0.000 claims 5
- 150000004665 fatty acids Chemical class 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 239000002253 acid Substances 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 150000001261 hydroxy acids Chemical class 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 4
- 150000004715 keto acids Chemical class 0.000 claims 3
- 150000001298 alcohols Chemical class 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- 150000002170 ethers Chemical class 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- HYIMSNHJOBLJNT-UHFFFAOYSA-N Nifedipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1[N+]([O-])=O HYIMSNHJOBLJNT-UHFFFAOYSA-N 0.000 claims 1
- 239000006096 absorbing agent Substances 0.000 claims 1
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 230000002093 peripheral Effects 0.000 claims 1
- 241000283898 Ovis Species 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
Description
[例6]
[血液改質剤を含む血液の表面張力]
血液改質剤を含む血液の表面張力を、協和界面科学社製接触角計 Drop Master500を用い、ペンダントドロップ法にて測定した。表面張力は、ヒツジ脱繊維血に、所定の量の血液改質剤を添加し、十分振とうした後に測定した。
測定は、機器が自動で行うが、表面張力γは、以下の式により求められる(図14を参照)。
[Example 6]
[Surface tension of blood containing blood modifying agents]
The surface tension of blood containing a blood modifying agent was measured by a pendant drop method using a contact angle meter Drop Master 500 manufactured by Kyowa Interface Science Co., Ltd. The surface tension was measured after adding a predetermined amount of blood modifying agent to sheep defibrinated blood and shaking sufficiently.
Although the measurement is automatically performed by the instrument, the surface tension γ is obtained by the following equation (see FIG. 14).
Claims (11)
前記液体透過性シートのうち液体の供給を受ける液体被供給領域に、伸張可能な蛇腹部を有する伸張性領域と、前記伸張性領域を包囲する可撓性領域とが形成されており、
前記伸張性領域に液体透過孔が形成されており、前記可撓性領域に液体透過孔が形成されていない、前記吸収性物品。 An absorbent article comprising a liquid permeable sheet, a liquid impermeable sheet, and an absorber provided between the liquid permeable sheet and the liquid impermeable sheet,
A stretchable region having an expandable bellows portion and a flexible region surrounding the stretchable region are formed in a liquid supply region that receives a supply of liquid in the liquid permeable sheet ,
The absorbent article, wherein a liquid permeable hole is formed in the extensible region and a liquid permeable hole is not formed in the flexible region .
(i)炭化水素;
(ii) (ii−1)炭化水素部分と、(ii−2)前記炭化水素部分のC−C単結合間に挿入された、カルボニル基(−CO−)及びオキシ基(−O−)から成る群から選択される、一又は複数の、同一又は異なる基とを有する化合物;及び
(iii) (iii−1)炭化水素部分と、(iii−2)前記炭化水素部分のC−C単結合間に挿入された、カルボニル基(−CO−)及びオキシ基(−O−)から成る群から選択される、一又は複数の、同一又は異なる基と、(iii−3)前記炭化水素部分の水素原子を置換する、カルボキシル基(−COOH)及びヒドロキシル基(−OH)から成る群から選択される、一又は複数の、同一又は異なる基とを有する化合物;
並びにそれらの任意の組み合わせから成る群から選択され、
ここで、(ii)又は(iii)の化合物において、オキシ基が2つ以上挿入されている場合には、各オキシ基は隣接していない、
請求項7に記載の吸収性物品。 The blood modifying agent is the following (i) to (iii):
(I) hydrocarbons;
(Ii) from (ii-1) a hydrocarbon moiety and (ii-2) a carbonyl group (—CO—) and an oxy group (—O—) inserted between the C—C single bonds of the hydrocarbon moiety. A compound having one or more identical or different groups selected from the group consisting of: and (iii) (iii-1) a hydrocarbon moiety and (iii-2) a CC single bond of said hydrocarbon moiety One or more of the same or different groups selected from the group consisting of a carbonyl group (—CO—) and an oxy group (—O—), inserted between them, and (iii-3) of the hydrocarbon moiety A compound having one or a plurality of the same or different groups selected from the group consisting of a carboxyl group (—COOH) and a hydroxyl group (—OH), which replaces a hydrogen atom;
As well as selected from the group consisting of any combination thereof,
Here, in the compound of (ii) or (iii), when two or more oxy groups are inserted, each oxy group is not adjacent,
The absorbent article according to claim 7 .
(i’)炭化水素;
(ii’) (ii’−1)炭化水素部分と、(ii’−2)前記炭化水素部分のC−C単結合間に挿入された、カルボニル結合(−CO−)、エステル結合(−COO−)、カーボネート結合(−OCOO−)、及びエーテル結合(−O−)から成る群から選択される、一又は複数の、同一又は異なる結合とを有する化合物;及び
(iii’) (iii’−1)炭化水素部分と、(iii’−2)前記炭化水素部分のC−C単結合間に挿入された、カルボニル結合(−CO−)、エステル結合(−COO−)、カーボネート結合(−OCOO−)、及びエーテル結合(−O−)から成る群から選択される、一又は複数の、同一又は異なる結合と、(iii’−3)前記炭化水素部分の水素原子を置換する、カルボキシル基(−COOH)及びヒドロキシル基(−OH)から成る群から選択される、一又は複数の、同一又は異なる基とを有する化合物;
並びにそれらの任意の組み合わせから成る群から選択され、
ここで、(ii’)又は(iii’)の化合物において、2以上の同一又は異なる結合が挿入されている場合には、各結合は隣接していない、
請求項7又は8に記載の吸収性物品。 The blood modifying agent is the following (i ′) to (iii ′):
(I ′) a hydrocarbon;
(Ii ′) (ii′-1) a hydrocarbon moiety and (ii′-2) a carbonyl bond (—CO—), an ester bond (—COO) inserted between the C—C single bonds of the hydrocarbon moiety. -), A carbonate bond (-OCOO-), and an ether bond (-O-) selected from the group consisting of one or more compounds having the same or different bonds; and (iii ') (iii'- 1) a hydrocarbon moiety and (iii′-2) a carbonyl bond (—CO—), an ester bond (—COO—), a carbonate bond (—OCOO) inserted between the C—C single bonds of the hydrocarbon moiety. -), And one or a plurality of the same or different bonds selected from the group consisting of an ether bond (-O-), and (iii'-3) a carboxyl group that replaces a hydrogen atom of the hydrocarbon moiety ( -COOH) and hydroxy A compound having one or more of the same or different groups selected from the group consisting of a sil group (—OH);
As well as selected from the group consisting of any combination thereof,
Here, in the compound of (ii ′) or (iii ′), when two or more identical or different bonds are inserted, each bond is not adjacent,
The absorbent article according to claim 7 or 8 .
(A) (A1)鎖状炭化水素部分と、前記鎖状炭化水素部分の水素原子を置換する2〜4個のヒドロキシル基とを有する化合物と、(A2)鎖状炭化水素部分と、前記鎖状炭化水素部分の水素原子を置換する1個のカルボキシル基とを有する化合物とのエステル;
(B) (B1)鎖状炭化水素部分と、前記鎖状炭化水素部分の水素原子を置換する2〜4個のヒドロキシル基とを有する化合物と、(B2)鎖状炭化水素部分と、前記鎖状炭化水素部分の水素原子を置換する1個のヒドロキシル基とを有する化合物とのエーテル;
(C) (C1)鎖状炭化水素部分と、前記鎖状炭化水素部分の水素原子を置換する、2〜4個のカルボキシル基とを含むカルボン酸、ヒドロキシ酸、アルコキシ酸又はオキソ酸と、(C2)鎖状炭化水素部分と、前記鎖状炭化水素部分の水素原子を置換する1個のヒドロキシル基とを有する化合物とのエステル;
(D)鎖状炭化水素部分と、前記鎖状炭化水素部分のC−C単結合間に挿入された、エーテル結合(−O−)、カルボニル結合(−CO−)、エステル結合(−COO−)、及びカーボネート結合(−OCOO−)から成る群から選択されるいずれか1つの結合とを有する化合物;
(E)ポリオキシC2〜6アルキレングリコール、又はそのアルキルエステル若しくはアルキルエーテル;及び
(F)鎖状炭化水素;
並びにそれらの任意の組み合わせから成る群から選択される、請求項7〜9のいずれか1項に記載の吸収性物品。 The blood modifying agent includes the following (A) to (F):
(A) (A1) a compound having a chain hydrocarbon moiety and 2 to 4 hydroxyl groups replacing hydrogen atoms in the chain hydrocarbon moiety, (A2) a chain hydrocarbon moiety, and the chain An ester with a compound having one carboxyl group that replaces a hydrogen atom in the hydrocarbon moiety;
(B) (B1) a compound having a chain hydrocarbon moiety and 2 to 4 hydroxyl groups replacing hydrogen atoms in the chain hydrocarbon moiety, (B2) a chain hydrocarbon moiety, and the chain An ether with a compound having one hydroxyl group replacing a hydrogen atom of the hydrocarbon moiety;
(C) (C1) a carboxylic acid, a hydroxy acid, an alkoxy acid or an oxo acid containing a chain hydrocarbon moiety and 2 to 4 carboxyl groups replacing the hydrogen atom of the chain hydrocarbon moiety; C2) an ester of a chain hydrocarbon moiety and a compound having one hydroxyl group replacing a hydrogen atom of the chain hydrocarbon moiety;
(D) an ether bond (—O—), a carbonyl bond (—CO—), an ester bond (—COO—) inserted between the chain hydrocarbon moiety and the C—C single bond of the chain hydrocarbon moiety. And a compound having any one bond selected from the group consisting of a carbonate bond (—OCOO—);
(E) polyoxy C 2-6 alkylene glycol, or an alkyl ester or alkyl ether thereof; and (F) a chain hydrocarbon;
And it is selected from the group consisting of any combination thereof, the absorbent article according to any one of claims 7-9.
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012082514A JP5726123B2 (en) | 2012-03-30 | 2012-03-30 | Absorbent articles |
EP13755536.3A EP2821040B1 (en) | 2012-02-29 | 2013-02-25 | Absorbent article |
AU2013227192A AU2013227192B2 (en) | 2012-02-29 | 2013-02-25 | Absorbent article |
US14/381,952 US9387135B2 (en) | 2012-02-29 | 2013-02-25 | Absorbent article |
CN201380022687.2A CN104271094B (en) | 2012-02-29 | 2013-02-25 | Absorbent commodity |
PCT/JP2013/054796 WO2013129327A1 (en) | 2012-02-29 | 2013-02-25 | Absorbent article |
TW102106978A TWI577353B (en) | 2012-02-29 | 2013-02-27 | Absorbent items |
ARP130100638A AR090195A1 (en) | 2012-02-29 | 2013-02-28 | ABSORBENT ARTICLE |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012082514A JP5726123B2 (en) | 2012-03-30 | 2012-03-30 | Absorbent articles |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2013208410A JP2013208410A (en) | 2013-10-10 |
JP2013208410A5 true JP2013208410A5 (en) | 2015-04-02 |
JP5726123B2 JP5726123B2 (en) | 2015-05-27 |
Family
ID=49526890
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012082514A Active JP5726123B2 (en) | 2012-02-29 | 2012-03-30 | Absorbent articles |
Country Status (1)
Country | Link |
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JP (1) | JP5726123B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5843740B2 (en) * | 2012-02-29 | 2016-01-13 | ユニ・チャーム株式会社 | Absorbent articles |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5650214A (en) * | 1996-05-31 | 1997-07-22 | The Procter & Gamble Company | Web materials exhibiting elastic-like behavior and soft, cloth-like texture |
JP2009201878A (en) * | 2008-02-29 | 2009-09-10 | Uni Charm Corp | Absorbent article |
JP5466489B2 (en) * | 2009-11-16 | 2014-04-09 | 花王株式会社 | Absorbent articles |
-
2012
- 2012-03-30 JP JP2012082514A patent/JP5726123B2/en active Active
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