JP2020097731A - 吸水性樹脂粒子、これを含む吸収体及び吸収性物品 - Google Patents
吸水性樹脂粒子、これを含む吸収体及び吸収性物品 Download PDFInfo
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- JP2020097731A JP2020097731A JP2019213106A JP2019213106A JP2020097731A JP 2020097731 A JP2020097731 A JP 2020097731A JP 2019213106 A JP2019213106 A JP 2019213106A JP 2019213106 A JP2019213106 A JP 2019213106A JP 2020097731 A JP2020097731 A JP 2020097731A
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- Prior art keywords
- water
- resin particles
- absorbent resin
- acid
- polyether
- Prior art date
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- BBZZYYNHMXFHKE-UHFFFAOYSA-N n-hexacosyl-n-octylacetamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCN(C(C)=O)CCCCCCCC BBZZYYNHMXFHKE-UHFFFAOYSA-N 0.000 description 1
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- SRIVPZIUICSLRG-UHFFFAOYSA-N n-octylheptacosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCCCCCCC SRIVPZIUICSLRG-UHFFFAOYSA-N 0.000 description 1
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- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
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- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
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- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
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- 159000000000 sodium salts Chemical class 0.000 description 1
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- VOZKAJLKRJDJLL-UHFFFAOYSA-N tolylenediamine group Chemical group CC1=C(C=C(C=C1)N)N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
(i)炭素数8〜30の芳香族エチレン性モノマー
スチレン、α−メチルスチレン、ビニルトルエン及びヒドロキシスチレン等のスチレン、並びにビニルナフタレン及びジクロルスチレン等のスチレンのハロゲン置換体等。
(ii)炭素数2〜20の脂肪族エチレン性モノマー
アルケン(エチレン、プロピレン、ブテン、イソブチレン、ペンテン、ヘプテン、ジイソブチレン、オクテン、ドデセン及びオクタデセン等);並びにアルカジエン(ブタジエン及びイソプレン等)等。
(iii)炭素数5〜15の脂環式エチレン性モノマー
モノエチレン性不飽和モノマー(ピネン、リモネン及びインデン等);並びにポリエチレン性ビニルモノマー[シクロペンタジエン、ビシクロペンタジエン及びエチリデンノルボルネン等]等。
水溶液重合を行う場合、有機溶媒の使用量(重量%)は、水の重量を基準として40以下が好ましく、更に好ましくは30以下である。
ラジカル重合触媒の使用量(重量%)は、水溶性ビニルモノマー(a1)及び加水分解性ビニルモノマー(a2)の、その他のビニルモノマー(a3)を用いる場合は(a1)〜(a3)の、合計重量に基づいて、0.0005〜5が好ましく、更に好ましくは0.001〜2である。
重合コントロール剤の使用量(重量%)は、水溶性ビニルモノマー(a1)及び加水分解性ビニルモノマー(a2)の、その他のビニルモノマー(a3)を用いる場合は(a1)〜(a3)の、合計重量に基づいて、0.0005〜5が好ましく、更に好ましくは0.001〜2である。
なお、HLB値は、親水性−疎水性バランス(HLB)値を意味し、小田法(界面活性剤入門、212頁、藤本武彦、三洋化成工業株式会社発行、2007年発行)により求められる。
多価アルコール脂肪酸エステルAO付加物の具体例としては、エチレングリコールモノオレートEO付加物、エチレングリコールモノステアレートEO付加物、トリメチロールプロパンモノステアレートEO・POランダム付加物、ソルビタンモノラウレートEO付加物、ソルビタンモノステアレートEO付加物、ソルビタンジステアレートEO付加物、ソルビタンジラウレートEO・POランダム付加物などが挙げられる。
多価アルコールアルキルエーテルの具体例としては、ペンタエリスリトールモノブチルエーテル、ペンタエリスリトールモノラウリルエーテル、ソルビタンモノメチルエーテル、ソルビタンモノステアリルエーテル、メチルグリコシド、ラウリルグリコシドなどが挙げられる。
多価アルコールアルキルエーテルAO付加物の具体例としては、ソルビタンモノステアリルエーテルEO付加物、メチルグリコシドEO・POランダム付加物、ラウリルグリコシドEO付加物、ステアリルグリコシドEO・POランダム付加物などが挙げられる。
・信越化学工業株式会社製
KF−945{側鎖、オキシエチレン及びオキシプロピレン}、KF−6020{側鎖、オキシエチレン及びオキシプロピレン}、KF−351A{側鎖、オキシエチレン及びオキシプロピレン}、X−22−6191{側鎖、オキシエチレン及びオキシプロピレン}、X−22−4952{側鎖、オキシエチレン及びオキシプロピレン}、X−22−4272{側鎖、オキシエチレン及びオキシプロピレン}、X−22−6266{側鎖、オキシエチレン及びオキシプロピレン}
FZ−2110{両末端、オキシエチレン及びオキシプロピレン}、FZ−2122{両末端、オキシエチレン及びオキシプロピレン}、FZ−7006{両末端、オキシエチレン及びオキシプロピレン}、FZ−2166{両末端、オキシエチレン及びオキシプロピレン}、FZ−2164{両末端、オキシエチレン及びオキシプロピレン}、FZ−2154{両末端、オキシエチレン及びオキシプロピレン}、FZ−2203{両末端、オキシエチレン及びオキシプロピレン}及びFZ−2207{両末端、オキシエチレン及びオキシプロピレン}
・信越化学工業株式会社製
X−22−3701E{側鎖、4000}、X−22−162C{両末端、2300}、X−22−3710{片末端、1450}
BY16−880{側鎖、3500}、BY16−750{両末端、750}、BY16−840{側鎖、3500}、SF8418{側鎖、3500}
・信越化学工業株式会社製
X−22−343{側鎖、525}、KF−101{側鎖、350}、KF−1001{側鎖、3500}、X−22−2000{側鎖、620}、X−22−2046{側鎖、600}、KF−102{側鎖、3600}、X−22−4741{側鎖、2500}、KF−1002{側鎖、4300}、X−22−3000T{側鎖、250}、X−22−163{両末端、200}、KF−105{両末端、490}、X−22−163A{両末端、1000}、X−22−163B{両末端、1750}、X−22−163C{両末端、2700}、X−22−169AS{両末端、500}、X−22−169B{両末端、1700}、X−22−173DX{片末端、4500}、X−22−9002{側鎖・両末端、5000}
FZ−3720{側鎖、1200}、BY16−839{側鎖、3700}、SF8411{側鎖、3200}、SF8413{側鎖、3800}、SF8421{側鎖、11000}、BY16−876{側鎖、2800}、FZ−3736{側鎖、5000}、BY16−855D{側鎖、180}、BY16−8{側鎖、3700}
・信越化学工業株式会社製
KF−865{側鎖、5000}、KF−864{側鎖、3800}、KF−859{側鎖、6000}、KF−393{側鎖、350}、KF−860{側鎖、7600}、KF−880{側鎖、1800}、KF−8004{側鎖、1500}、KF−8002{側鎖、1700}、KF−8005{側鎖、11000}、KF−867{側鎖、1700}、X−22−3820W{側鎖、55000}、KF−869{側鎖、8800}、KF−861{側鎖、2000}、X−22−3939A{側鎖、1500}、KF−877{側鎖、5200}、PAM−E{両末端、130}、KF−8010{両末端、430}、X−22−161A{両末端、800}、X−22−161B{両末端、1500}、KF−8012{両末端、2200}、KF−8008{両末端、5700}、X−22−1660B−3{両末端、2200}、KF−857{側鎖、2200}、KF−8001{側鎖、1900}、KF−862{側鎖、1900}、X−22−9192{側鎖、6500}
FZ−3707{側鎖、1500}、FZ−3504{側鎖、1000}、BY16−205{側鎖、4000}、FZ−3760{側鎖、1500}、FZ−3705{側鎖、4000}、BY16−209{側鎖、1800}、FZ−3710{側鎖、1800}、SF8417{側鎖、1800}、BY16−849{側鎖、600}、BY16−850{側鎖、3300}、BY16−879B{側鎖、8000}、BY16−892{側鎖、2000}、FZ−3501{側鎖、3000}、FZ−3785{側鎖、6000}、BY16−872{側鎖、1800}、BY16−213{側鎖、2700}、BY16−203{側鎖、1900}、BY16−898{側鎖、2900}、BY16−890{側鎖、1900}、BY16−893{側鎖、4000}、FZ−3789{側鎖、1900}、BY16−871{両末端、130}、BY16−853C{両末端、360}、BY16−853U{両末端、450}
・装置:「Waters Alliance 2695」[Waters社製]
・カラム:「Guardcolumn Super H−L」(1本)、「TSKgel SuperH2000、TSKgel SuperH3000、TSKgel SuperH4000を各1本連結したもの」[いずれも東ソー(株)製]
・試料溶液:0.25重量%のテトラヒドロフラン溶液
・溶液注入量:10μL
・流量:0.6mL/分
・測定温度:40℃
・検出装置:屈折率検出器
・基準物質:標準ポリエチレングリコール
DW(Demand Wettability)法は、25±2℃、湿度50±10%の室内で、図1に示す装置を用いて行う測定方法である。図1に示した測定装置は、ビュレット部(2){目盛容量50ml、長さ86cm、内径1.05cm、}と導管{内径7mm}、測定台(6)からなっている。ビュレット部(2)は、上部にゴム栓(1)、下部に吸気導入管(9){先端内径3mm}とコック(7)が連結されており、さらに、吸気導入管(9)の上部はコック(8)がある。ビュレット部(2)から測定台(6)までは、導管が取り付けられている。測定台(6)の中央部には、生理食塩水供給部として直径3ミリの穴があいており、導管が連結されている。
目開き63μm(JIS Z8801−1:2006)のナイロン網で作成したティーバッグ(縦20cm、横10cm)に測定試料1.00gを入れ、生理食塩水(食塩濃度0.9重量%)1,000ml中に無撹拌下、1時間浸漬した後、15分間吊るして水切りする。その後、ティーバッグごと、遠心分離器にいれ、150Gで90秒間遠心脱水して余剰の生理食塩水を取り除き、ティーバックを含めた重量(h1)を測定し次式から保水量を求める。
保水量(g/g)=(h1)−(h2)
なお、使用した生理食塩水及び測定雰囲気の温度は25℃±2℃とする。測定試料を用いない以外は上記と同様にして、遠心脱水後のティーバックの重量を測定し(h2)とする。
目開き63μm(JIS Z8801−1:2006)のナイロン網を底面に貼った円筒型プラスチックチューブ(内径:25mm、高さ:34mm)内に、標準ふるいを用いて250〜500μmの範囲にふるい分けした測定試料0.16gを秤量し、円筒型プラスチックチューブを垂直にしてナイロン網上に測定試料がほぼ均一厚さになるように整えた後、この測定試料の上に分銅(重量:210.6g、外径:24.5mm、)を乗せる。この円筒型プラスチックチューブ全体の重量(h3)を計量した後、生理食塩水(食塩濃度0.9%)60mlの入ったシャーレ(直径:12cm)の中に測定試料及び分銅の入った円筒型プラスチックチューブを垂直に立ててナイロン網側を下面にして浸し、60分静置する。60分後に、円筒型プラスチックチューブをシャーレから引き上げ、これを斜めに傾けて底部に付着した水を一箇所に集めて水滴として垂らすことで余分な水を除去した後、測定試料及び分銅の入った円筒型プラスチックチューブ全体の重量(h4)を計量し、次式から荷重下吸収量を求める。なお、使用した生理食塩水及び測定雰囲気の温度は25℃±2℃とする。
荷重下吸収量(g/g)={(h4)−(h3)}/0.16
アクリル酸(a1−1){三菱化学株式会社製、純度100%}270部、内部架橋剤(b−1){ペンタエリスリトールトリアリルエーテル、ダイソ−株式会社製}0.98部(アクリル酸に基づいて0.10モル%)及びイオン交換水712部を攪拌・混合しながら3℃に保った。この混合物中に窒素を流入して溶存酸素量を1ppm以下とした後、1%過酸化水素水溶液1.1部、2%アスコルビン酸水溶液2.0部及び2%の2,2’−アゾビスアミジノプロパンジハイドロクロライド水溶液13.5部を添加・混合して重合を開始させた。混合物の温度が80℃に達した後、80±2℃で約5時間熟成することにより含水ゲルを得た。
製造例1において、疎水性物質(c)としてショ糖ステアリン酸エステルをポリエーテル変性ポリシロキサン(商品名:KF−6020、側鎖:オキシエチレン及びオキシプロピレン、信越化学工業株式会社製)に変更した以外は同様の操作を行い、表面架橋された樹脂粒子(A−3)を得た。
アクリル酸(a1−1){三菱化学株式会社製、純度100%}270部、内部架橋剤(b−1){ペンタエリスリトールトリアリルエーテル、ダイソ−株式会社製}0.98部(アクリル酸に基づいて0.10モル%)及びイオン交換水712部を攪拌・混合しながら3℃に保った。この混合物中に窒素を流入して溶存酸素量を1ppm以下とした後、1%過酸化水素水溶液1.1部、2%アスコルビン酸水溶液2.0部及び2%の2,2’−アゾビスアミジノプロパンジハイドロクロライド水溶液13.5部を添加・混合して重合を開始させた。混合物の温度が80℃に達した後、80±2℃で約5時間熟成することにより含水ゲルを得た。
アクリル酸(a1−1){三菱化学株式会社製、純度100%}270部、内部架橋剤(b−1){ペンタエリスリトールトリアリルエーテル、ダイソ−株式会社製}0.68部(アクリル酸に基づいて0.07モル%)及びイオン交換水712部を攪拌・混合しながら3℃に保った。この混合物中に窒素を流入して溶存酸素量を1ppm以下とした後、1%過酸化水素水溶液1.1部、2%アスコルビン酸水溶液2.0部及び2%の2,2’−アゾビスアミジノプロパンジハイドロクロライド水溶液13.5部を添加・混合して重合を開始させた。混合物の温度が80℃に達した後、80±2℃で約5時間熟成することにより含水ゲルを得た。
アクリル酸(a1−1){三菱化学株式会社製、純度100%}270部、内部架橋剤(b−1){ペンタエリスリトールトリアリルエーテル、ダイソ−株式会社製}0.98部(アクリル酸に基づいて0.07モル%)及びイオン交換水712部を攪拌・混合しながら3℃に保った。この混合物中に窒素を流入して溶存酸素量を1ppm以下とした後、1%過酸化水素水溶液1.1部、2%アスコルビン酸水溶液2.0部及び2%の2,2’−アゾビスアミジノプロパンジハイドロクロライド水溶液13.5部を添加・混合して重合を開始させた。混合物の温度が80℃に達した後、80±2℃で約5時間熟成することにより含水ゲルを得た。
製造例5においてポリエーテル変性ポリシロキサン0.03部を0.002部に変更し、カルボキシ変性ポリシロキサン0.02部添加すること以外は同様の操作を行い、表面架橋された樹脂粒子(A−10)を得た。
製造例1において、疎水性物質(c)としてショ糖ステアリン酸エステルを使用しない以外は同様の操作を行い、表面架橋された樹脂粒子(A−11)を得た。
国際公開第2015/178481号パンフレットに記載された製造例2を参考に同様の操作を行い、ブロックポリマー(B)を得た。(B)のMnは、28,000であった。また、このMnと1H−NMR分析より求めた(B)の平均繰り返し数Nnは3.4であった。
製造例1で得られた表面架橋された樹脂粒子(A−2)100部を高速攪拌(ホソカワミクロン株式会社製高速攪拌タービュライザー、回転数2000rpm)しながら、ポリエチレングリコール20000(商品名:PEG−20000、三洋化成工業社製、Mn=20000)を1.0部、及びイオン交換水4.0部を均一に混合した。その後80℃で30分間加熱して、本発明の吸水性樹脂粒子(P−1)を得た。
実施例1のポリエチレングリコール20000をポリエチレングリコール2000(商品名:PEG−2000、三洋化成工業社製、Mn=2000)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−2)を得た。
実施例1のポリエチレングリコール20000の添加量を1.0部から、3.0部に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−3)を得た。
ポリエチレングリコール20000をポリエチレングリコール111000(商品名:Polyethylene glycol 111000、aldrich社製、Mn=96500)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−4)を得た。
実施例1のポリエチレングリコール20000をポリオキシエチレン・ポリオキシプロピレングリコールのブロック共重合体(商品名:ニューポールPE−68、三洋化成工業社製、Mn=8000)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−5)を得た。
実施例1の表面架橋された樹脂粒子(A−2)を表面架橋された樹脂粒子(A−3)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−6)を得た。
実施例1の表面架橋された樹脂粒子(A−2)を表面架橋された樹脂粒子(A−5)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−7)を得た。
実施例1の表面架橋された樹脂粒子(A−2)を表面架橋された樹脂粒子(A−7)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−8)を得た。
実施例1の表面架橋された樹脂粒子(A−2)を表面架橋された樹脂粒子(A−9)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−9)を得た。
実施例1の表面架橋された樹脂粒子(A−2)を表面架橋された樹脂粒子(A−10)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−10)を得た。
実施例1の表面架橋された樹脂粒子(A−2)を表面架橋された樹脂粒子(A−10)に、ポリエチレングリコール20000をニューポールPE−128(商品名:ニューポールPE−128、三洋化成工業社製、Mn=31000)に変更した以外は実施例1と同様の操作を行い、本発明の吸水性樹脂粒子(P−11)を得た。
実施例1のポリエチレングリコール20000をポリエチレングリコール1000(商品名:PEG−1000、三洋化成工業社製、Mn=1000)に変更した以外は実施例1と同様の操作を行い、比較用の吸水性樹脂粒子(R−1)を得た。
実施例1の表面架橋された樹脂粒子(A−2)を樹脂粒子(A−4)に変更した以外は実施例と同様の操作を行い、比較用の吸水性樹脂粒子(R−2)を得た。
実施例1において、表面架橋された樹脂粒子(A−2)を樹脂粒子(A−4)に変更したこと、ポリエチレングリコール20000を使用しないこと以外は実施例1と同様の操作を行い、比較用の吸水性樹脂粒子(R−3)を得た。
実施例1のポリエチレングリコール20000を製造例8で得られたブロックポリマー(B)に変更した以外は実施例1と同様の操作を行い、比較用の吸水性樹脂粒子(R−4)を得た。
フラッフパルプ100部と評価試料{各実施例及び比較例の吸水性樹脂粒子}100部とを気流型混合装置{株式会社オーテック社製パッドフォーマー}で混合して、混合物を得た後、この混合物を坪量約500g/m2となるように均一にアクリル板(厚み4mm)上に積層し、5kg/cm2の圧力で30秒間プレスし、吸収体を得た。この吸収体の10cm×10cmの試験片を細断した後、試験片の重量(m1)を測定した。次いで、これを金属製のバット上に置き、80℃に設定・温調済の循風乾燥機内で10分間静置した後室温まで放冷して、吸水性樹脂粒子がフラッフパルプに固着した吸収体を得た。ただし、比較例4で得た吸水性樹脂粒子(R−4)で作成した吸収体については、循風乾燥機の設定温度を80℃から150℃に変更して実施した。その後、固着した吸収体をJIS標準ふるいの目開き4mmの金網の上に置いた。この金網をロータップ試験篩振とう機(ロータップ型、(株)飯田製作所製)に入れて、5分間振振動を与えた後、最後にこの試験片の上下を反転させて、フラッフパルプに固着していない吸水性樹脂粒子を脱離させた後、金網上に残った試験片の重量(m2)を測定し、以下の式で固着率を算出した。ただし、10cm×10cmの試験片に含まれる吸水性樹脂粒子の重量を2.5gとして、算出した。
(固着率[%])={2.5[g]−(m1[g]−m2[g])}/2.5[g]×100
前述した吸水性樹脂がフラッフパルプに固着した吸収体を10cm×40cmの長方形に裁断し、各々の上下に吸収体と同じ大きさの吸水紙(坪量15.5g/m2、アドバンテック社製、フィルターペーパー2番)を配置し、さらにポリエチレンシート(タマポリ社製ポリエチレンフィルムUB−1)を裏面に、不織布(坪量20g/m2、旭化成社製エルタスガード)を表面に配置することにより紙おむつを調製した。吸水性樹脂粒子と繊維の重量比率(吸水性樹脂粒子の重量/繊維の重量)は50/50であった。
SDME(Surface Dryness Measurement Equipment)試験器(WK system社製)の検出器を十分に湿らした紙おむつ{人工尿(塩化カリウム0.03重量%、硫酸マグネシウム0.08重量%、塩化ナトリウム0.8重量%及び脱イオン水99.09重量%)の中に紙おむつを浸し、60分放置して調製した。}の上に置き、0%ドライネス値を設定し、次に、SDME試験器の検出器を乾いた紙おむつ{紙おむつを80℃、2時間加熱乾燥して調製した。}の上に置き100%ドライネス値を設定し、SDME試験器の校正を行った。次に、測定する紙おむつの中央に金属リング(内径70mm、長さ50mm)をセットし、人工尿80mlを注入し、人工尿を吸収し終えたら{人工尿による光沢が確認できなくなったら}、直ちに金属リングを取り去り、紙おむつの中央及びその左右{紙おむつ40cmの端から10cmの等間隔に3箇所}にSDME検出器を3つ載せて、表面ドライネス値(単位:%)の測定を開始し、測定開始から5分後の値を、3つのSDME検出器のうち、中央の検出器のドライネス値を表面ドライネス値(SD1−1){中央}、残りの2つのSDME検出器のドライネス値を表面ドライネス値(SD1−2){左}、表面ドライネス値(SD1−3){右}とした。なお、人工尿、測定雰囲気及び放置雰囲気は、25±5℃、65±10%RHで行った。
2 ビュレット部
3 生理食塩水
4 吸水性樹脂粒子
5 平織りナイロンメッシュ
6 測定台
7 コック
8 コック
9 空気導入管
Claims (10)
- 水溶性ビニルモノマー(a1)及び/又は加水分解により水溶性ビニルモノマー(a1)となるビニルモノマー(a2)並びに内部架橋剤(b)を必須構成単位とする架橋重合体(A)と疎水性物質(c)とを含んでなる吸水性樹脂粒子であって、吸水性樹脂粒子の表面にポリオキシアルキレン鎖を有するポリエーテル(d)を含有し、(d)の数平均分子量が2000以上である吸水性樹脂粒子。
- ポリエーテル(d)の数平均分子量が5000〜10万である請求項1に記載の吸水性樹脂粒子。
- ポリエーテル(d)が水溶性である請求項1又は2に記載の吸水性樹脂粒子。
- ポリエーテル(d)はポリオキシエチレン鎖を有するポリエーテルである請求項1〜3のいずれかに記載の吸水性樹脂粒子。
- ポリエーテル(d)がポリエチレングリコール、ポリオキシエチレンアルキルエーテル、及びポリオキシエチレン・ポリオキシプロピレングリコールのブロック共重合体からなる群より選ばれる少なくとも1種である請求項1〜4のいずれかに記載の吸水性樹脂粒子。
- ポリエーテル(d)の含有量が吸水性樹脂粒子の重量に基づいて0.5〜5.0重量%である請求項1〜5のいずれかに記載の吸水性樹脂粒子。
- 疎水性物質(c)が炭素数8〜30の炭化水素基を含有する疎水性物質(c1)及び/又は有機ポリシロキサンである疎水性物質(c2)である請求項1〜6のいずれかに記載の吸水性樹脂粒子。
- Demand Wettability試験法(DW法)による30秒後吸収量が3〜8ml/gである請求項1〜7のいずれかに記載の吸水性樹脂粒子。
- 繊維状基材に固着化された請求項1〜8のいずれかに記載の吸水性樹脂粒子を含有してなる吸収体。
- 請求項9に記載の吸収体を用いた吸収性物品。
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JPS57168921A (en) * | 1981-04-10 | 1982-10-18 | Sumitomo Chem Co Ltd | Production of highly water-absorbing polymeric material having improved water-absorption rate |
JP2013203842A (ja) * | 2012-03-28 | 2013-10-07 | San-Dia Polymer Ltd | 吸収性樹脂粒子並びにこれを含む吸収体及び吸収性物品 |
JP2021505704A (ja) * | 2017-12-11 | 2021-02-18 | エルジー・ケム・リミテッド | 高吸水性樹脂およびその製造方法 |
JP2021517603A (ja) * | 2018-03-30 | 2021-07-26 | エルジー・ケム・リミテッド | 高吸水性樹脂およびその製造方法 |
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JPS57168921A (en) * | 1981-04-10 | 1982-10-18 | Sumitomo Chem Co Ltd | Production of highly water-absorbing polymeric material having improved water-absorption rate |
JP2013203842A (ja) * | 2012-03-28 | 2013-10-07 | San-Dia Polymer Ltd | 吸収性樹脂粒子並びにこれを含む吸収体及び吸収性物品 |
JP2021505704A (ja) * | 2017-12-11 | 2021-02-18 | エルジー・ケム・リミテッド | 高吸水性樹脂およびその製造方法 |
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WO2022124137A1 (ja) * | 2020-12-09 | 2022-06-16 | 住友精化株式会社 | 樹脂粒子組成物 |
CN116568761A (zh) * | 2020-12-09 | 2023-08-08 | 住友精化株式会社 | 树脂粒子组合物 |
CN116568761B (zh) * | 2020-12-09 | 2024-08-13 | 住友精化株式会社 | 树脂粒子组合物 |
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