JPH0476362B2 - - Google Patents
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- Publication number
- JPH0476362B2 JPH0476362B2 JP61081370A JP8137086A JPH0476362B2 JP H0476362 B2 JPH0476362 B2 JP H0476362B2 JP 61081370 A JP61081370 A JP 61081370A JP 8137086 A JP8137086 A JP 8137086A JP H0476362 B2 JPH0476362 B2 JP H0476362B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- polymerization
- oxidizing agent
- added
- aqueous solution
- 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.)
- Expired - Lifetime
Links
- 239000011347 resin Substances 0.000 claims description 26
- 229920005989 resin Polymers 0.000 claims description 26
- 239000007800 oxidant agent Substances 0.000 claims description 24
- 239000003638 chemical reducing agent Substances 0.000 claims description 19
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 238000006386 neutralization reaction Methods 0.000 claims description 7
- 150000001768 cations Chemical class 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical group OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 2
- 125000005385 peroxodisulfate group Chemical group 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 claims 1
- 229940079826 hydrogen sulfite Drugs 0.000 claims 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 29
- 239000007864 aqueous solution Substances 0.000 description 21
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 238000010521 absorption reaction Methods 0.000 description 14
- 239000000178 monomer Substances 0.000 description 14
- 239000002250 absorbent Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 230000002745 absorbent Effects 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 229940048053 acrylate Drugs 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 6
- -1 alkali metal acrylate Chemical class 0.000 description 5
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 5
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 4
- 230000020169 heat generation Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003505 polymerization initiator Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 3
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 2
- XNDZQQSKSQTQQD-UHFFFAOYSA-N 3-methylcyclohex-2-en-1-ol Chemical compound CC1=CC(O)CCC1 XNDZQQSKSQTQQD-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 150000004645 aluminates Chemical class 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 2
- 235000010263 potassium metabisulphite Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229940047670 sodium acrylate Drugs 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000011345 viscous material Substances 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- VAPQAGMSICPBKJ-UHFFFAOYSA-N 2-nitroacridine Chemical compound C1=CC=CC2=CC3=CC([N+](=O)[O-])=CC=C3N=C21 VAPQAGMSICPBKJ-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- HDYRYUINDGQKMC-UHFFFAOYSA-M acetyloxyaluminum;dihydrate Chemical compound O.O.CC(=O)O[Al] HDYRYUINDGQKMC-UHFFFAOYSA-M 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229940009827 aluminum acetate Drugs 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- 239000012935 ammoniumperoxodisulfate Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- FGRVOLIFQGXPCT-UHFFFAOYSA-L dipotassium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [K+].[K+].[O-]S([O-])(=O)=S FGRVOLIFQGXPCT-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000012688 inverse emulsion polymerization Methods 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- DJEHXEMURTVAOE-UHFFFAOYSA-M potassium bisulfite Chemical compound [K+].OS([O-])=O DJEHXEMURTVAOE-UHFFFAOYSA-M 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 235000010259 potassium hydrogen sulphite Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerization Catalysts (AREA)
Description
【発明の詳細な説明】
<産業上の利用分野>
この発明は、吸水性樹脂の製造方法に関する。
さらに詳細には、この発明は製造上の安全性に優
れかつ高い吸水能力を有する吸水性樹脂の製造方
法に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Field of Application> The present invention relates to a method for producing a water-absorbing resin.
More specifically, the present invention relates to a method for producing a water-absorbing resin having excellent manufacturing safety and high water-absorbing capacity.
<従来の技術および発明が解決しようとする問題
点>
近年、紙おむつ、生理用品、微生物や植物の培
地、液体クロマトグラフイーの担体等に、高い吸
水能力および保水能力を有する吸水性樹脂が用い
られている。このような吸水性樹脂の一種とし
て、架橋型ポリアクリル酸金属塩系が汎用されて
いる。<Prior art and problems to be solved by the invention> In recent years, water-absorbing resins with high water-absorbing and water-retaining abilities have been used for disposable diapers, sanitary products, culture media for microorganisms and plants, carriers for liquid chromatography, etc. ing. As a type of such water-absorbing resin, a crosslinked polyacrylic acid metal salt type is widely used.
このアィクリル酸金属塩系吸水性樹脂は、アク
リル酸ナトリウム、アクリル酸カリウム等のアク
リル酸アルカリ金属塩水溶液に、重合開始剤を添
加して重合させた後、水分を除去して製造されて
いる。この際、重合開始剤としては、例えば、過
硫酸カリウム、過硫酸ナトリウム等の過硫酸塩、
酸化剤と還元剤との組合せよりなるレドツクス触
媒(例えば、前記過硫酸酸塩と一価銅イオン、過
硫酸水素と二価鉄イオン等)が使用されるが、こ
れらの過硫酸塩やレドツクス触媒を開始剤として
用いると、重合反応が極めて急激で、例えば、重
合開始温度は常温でも重合の進行とともに急激に
発熱する。特に、工業的な生産のように、大量且
つ高モノマー濃度で実施される場合には、特別な
配慮をしない限りその制御は困難で、時には暴走
反応を生じ、危険性が極めて高いものである。か
かる観点から、暴走反応を防止するため、モノマ
ー濃度を低くすることや、温度制御システムを用
いて、前記アクリル酸塩の重合を行つているが、
モノマー濃度を低くすることは、水分の蒸発に多
大の熱量を要し非経済的であり、また温度制御シ
ステムを導入した装置も高価とる問題がある。 This metal acrylate-based water-absorbing resin is produced by adding a polymerization initiator to an aqueous solution of an alkali metal acrylate such as sodium acrylate or potassium acrylate, polymerizing the mixture, and then removing water. At this time, examples of the polymerization initiator include persulfates such as potassium persulfate and sodium persulfate;
A redox catalyst consisting of a combination of an oxidizing agent and a reducing agent (for example, the persulfate and monovalent copper ion, hydrogen persulfate and divalent iron ion, etc.) is used, but these persulfates and redox catalysts When used as an initiator, the polymerization reaction is extremely rapid; for example, even if the polymerization initiation temperature is room temperature, heat is generated rapidly as the polymerization progresses. In particular, when it is carried out in large quantities and at a high monomer concentration, such as in industrial production, it is difficult to control unless special consideration is taken, and runaway reactions sometimes occur, which is extremely dangerous. From this point of view, in order to prevent runaway reactions, the acrylate salt is polymerized by lowering the monomer concentration and using a temperature control system.
Lowering the monomer concentration requires a large amount of heat to evaporate water, which is uneconomical, and there is also the problem that equipment equipped with a temperature control system is expensive.
<目的>
この発明は上記問題点に鑑みてなされたもので
あり、特殊な重合開始剤を使用することにより、
極めて温和な条件下にアクリル酸金属塩の重合が
進行し、安全性が高いとともに高い吸水能力を有
する吸水性樹脂の製造方法を提供することを目的
とする。<Purpose> This invention was made in view of the above problems, and by using a special polymerization initiator,
It is an object of the present invention to provide a method for producing a water-absorbing resin in which polymerization of an acrylic acid metal salt proceeds under extremely mild conditions, which is highly safe and has a high water-absorbing capacity.
<問題を解決するための手段>
上記の問題点を解決すべくなされた、この発明
の吸水性樹脂の製造方法は、1価陽イオンによる
中和度が30%以上100%未満のアクリル酸を含硫
黄系還元剤で重合した後、酸化剤を添加し処理す
ることを特徴とするものである。<Means for solving the problem> The method for producing a water absorbent resin of the present invention, which was made to solve the above problems, uses acrylic acid whose degree of neutralization with monovalent cations is 30% or more and less than 100%. This method is characterized in that after polymerization with a sulfur-containing reducing agent, an oxidizing agent is added for treatment.
なお、この明細書において、中和度とは、仕込
みモノマー中のアクリル酸とアクリル酸塩の総計
に対するアクリル酸塩の比率をいい、下記の式で
定義される。 In this specification, the degree of neutralization refers to the ratio of acrylate to the total of acrylic acid and acrylate in the charged monomers, and is defined by the following formula.
中和度(%)
=アクリル酸塩(モル)×100/アクリル酸+アクリ
ル酸塩(モル)
上記の構成において、アクリル酸の中和に使用
される中和剤としては、最終製品たる吸水性樹脂
の使用目的に応じて適宜選択されるが、例えば、
水酸化ナトリウム、水酸化カリウム、水酸化リチ
ウム等のアルカリ金属水酸化物、炭酸ナトリウ
ム、炭酸カリウム、炭酸水素ナトリウム、炭酸水
素カリウム等のアルカリ金属炭酸塩または炭酸水
素塩、水酸化アンモニウム、トリエチルアミン、
エタノールアミン類、ピリジン、ピコリン等の有
機アミン類等、一価の陽イオンとして作用しえる
塩基の内から任意に選択できるが、経済性、安全
性および得られた吸水性樹脂の吸水性能等を考慮
すると水酸化ナトリウムが適切である。Degree of neutralization (%) = acrylate (mol) x 100/acrylic acid + acrylate (mol) In the above configuration, the neutralizing agent used to neutralize acrylic acid is It is selected as appropriate depending on the purpose of use of the resin, but for example,
Alkali metal hydroxides such as sodium hydroxide, potassium hydroxide, lithium hydroxide, alkali metal carbonates or hydrogen carbonates such as sodium carbonate, potassium carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, ammonium hydroxide, triethylamine,
Bases that can act as monovalent cations, such as ethanolamines, pyridine, picoline, and other organic amines, can be selected arbitrarily, but depending on economic efficiency, safety, and water absorption performance of the resulting water absorbent resin, etc. Considering this, sodium hydroxide is appropriate.
また、アクリル酸の中和度としては、30%以
上、好ましくは50%以上、さらに好ましくは70%
以上95%以下のものが、得られた吸水性樹脂の吸
水性能からして好ましい。また、アクリル酸の1
価陽イオン塩とアクリル酸を適宜な割合で混合し
て、前記のアクリル酸塩水溶液を調製してもよ
い。重合溶液の濃度は発熱の少ないというこの発
明の特徴からすると、溶液中のモノマー濃度は高
い程、この発明の技術的、装置的、性能的効果が
顕著となるが、水酸化ナトリウムで中性付近に中
和を行う場合、水分濃度が45%〜50%以下になる
とアクリル酸ナトリウムが析出するので、モノマ
ー濃度をより高くする場合には、混合攪拌等によ
り溶液の均質化を図る必要がある。 In addition, the degree of neutralization of acrylic acid is 30% or more, preferably 50% or more, and more preferably 70%.
A ratio of 95% or less is preferable in view of the water absorption performance of the resulting water absorbent resin. In addition, 1 of acrylic acid
The acrylate aqueous solution may be prepared by mixing a valence cation salt and acrylic acid in an appropriate ratio. Considering the feature of this invention that the concentration of the polymerization solution is low in heat generation, the higher the monomer concentration in the solution, the more remarkable the technical, equipment, and performance effects of this invention are. When performing neutralization, sodium acrylate will precipitate if the water concentration falls below 45% to 50%, so if the monomer concentration is to be increased, it is necessary to homogenize the solution by mixing and stirring.
また、この発明で得られる吸水性樹脂の吸水能
力、ゲル強度等を改質するために、前記のアクリ
ル酸にはアクリルアミド、メチレンビスアクリル
アミド、N−ビニルピロリドン等を添加して共重
合体としてもよい。 In addition, in order to modify the water absorption capacity, gel strength, etc. of the water absorbent resin obtained by this invention, acrylamide, methylenebisacrylamide, N-vinylpyrrolidone, etc. may be added to the acrylic acid to form a copolymer. good.
この発明で使用される含硫黄系還元剤として
は、アクリル酸塩の重合を開始できる含硫黄系還
元剤であれば、特に限定されないが、亜硫酸ナト
リウム、亜硫酸カリウム等の亜硫酸塩、亜硫酸水
素ナトリウム、亜硫酸水素カリウム等の亜硫酸水
素塩、チオ硫酸ナトリウム、チオ硫酸カリウム等
のチオ硫酸塩、亜ニチオン酸ナトリウム等の亜ニ
チオン酸塩等またはこれらの混合物が挙げられ
る。これらの含硫黄系還元剤は、粉末状態のまま
でも使用できるが、通常水溶液として使用され
る。 The sulfur-containing reducing agent used in this invention is not particularly limited as long as it is a sulfur-containing reducing agent that can initiate polymerization of acrylate, but sulfites such as sodium sulfite and potassium sulfite, sodium hydrogen sulfite, Examples include hydrogen sulfites such as potassium hydrogen sulfite, thiosulfates such as sodium thiosulfate and potassium thiosulfate, dithionites such as sodium dithionite, and mixtures thereof. Although these sulfur-containing reducing agents can be used in powder form, they are usually used as an aqueous solution.
また、酸化剤としては、慣用の酸化剤、例え
ば、ペルオキソ二硫酸ナトリウム、ペルオキソ二
硫酸カリウム、ペルオキソニ硫酸アンモニウム等
のペルオキソ二硫酸塩等が挙げられ、単独で、ま
たは混合物として使用される。また、粉末状態で
も使用できるが、通常水溶液として使用される。 Examples of the oxidizing agent include conventional oxidizing agents, such as peroxodisulfates such as sodium peroxodisulfate, potassium peroxodisulfate, and ammonium peroxodisulfate, which may be used alone or as a mixture. Although it can be used in powder form, it is usually used as an aqueous solution.
重合に使用される含硫黄系還元剤の量は、還元
剤の種類、酸化剤の使用量、重合温度、モノマー
水溶液の濃度等にもよるが、通常、モノマー仕込
み100重量部に対して、0.001〜0.5重量部、好ま
しくは0.01〜0.1重量部添加される。還元剤の添
加量が0.001重量部未満では反応が遅く重合時間
が長くなり、その後、酸化剤を添加した時に通常
の過酸化物等によりアクリル酸塩の重合に見られ
るような大きな発熱反応の傾向が生じ、吸水能力
も低下する。また0.5重量部を越えて添加すると
重合溶液は高粘度となり、モノマー濃度を下げな
いと攪拌混合が困難となる。 The amount of sulfur-containing reducing agent used in polymerization depends on the type of reducing agent, amount of oxidizing agent, polymerization temperature, concentration of monomer aqueous solution, etc., but is usually 0.001 parts by weight per 100 parts by weight of monomer. ~0.5 parts by weight, preferably 0.01 to 0.1 parts by weight are added. If the amount of the reducing agent added is less than 0.001 parts by weight, the reaction will be slow and the polymerization time will be long, and then when an oxidizing agent is added, there is a tendency for a large exothermic reaction like that seen in the polymerization of acrylates due to ordinary peroxides, etc. occurs, and the water absorption capacity also decreases. Further, if more than 0.5 parts by weight is added, the polymerization solution becomes highly viscous, and stirring and mixing becomes difficult unless the monomer concentration is lowered.
また、酸化剤の添加量は、酸化剤の種類、反応
温度、前記の還元剤の使用量、吸水性樹脂に要求
される特性等により異なるが、通常、モノマー仕
込み量100重量部に対して0.001〜0.5重量部、好
ましくは0.01〜0.1重量部添加される。酸化剤の
添加量が0.001重量部未満では得られた吸水性樹
脂に可溶性の部分が多くなり、0.5重量部を越え
て添加すると、得られた吸水性樹脂が硬くなり吸
水能力が低下する。 The amount of the oxidizing agent added varies depending on the type of oxidizing agent, the reaction temperature, the amount of the reducing agent used, the characteristics required of the water-absorbing resin, etc., but it is usually 0.001 parts by weight per 100 parts by weight of the monomer. ~0.5 parts by weight, preferably 0.01 to 0.1 parts by weight are added. If the amount of the oxidizing agent added is less than 0.001 part by weight, the resulting water absorbent resin will have a large soluble portion, and if it is added in excess of 0.5 part by weight, the resulting water absorbent resin will become hard and its water absorption capacity will decrease.
上述のように、この発明の製造方法で得られる
吸水性樹脂は、使用される還元剤および酸化剤の
使用量により、吸水能力、吸水後のゲル硬度等を
適宜変更することができる。一般式に、例えば、
酸化剤の添加量を一定にして、還元剤の使用量を
変更した場合、還元剤の使用量の増加と共に吸水
能力が大きくなるがある範囲を越えると可溶化傾
向が大きくなる。また、還元剤の使用量を一定に
して、酸化剤の使用量を増加すると、吸水量が減
少し、吸水後のゲル状態が硬くなり、少なくする
と軟らかくなる傾向にある。しかし、各々が前記
の添加範囲内で比例的に増加、減少して使用され
た場合には得られたポリマーの性能には大きな差
異が認められない。 As described above, the water-absorbing resin obtained by the production method of the present invention can have its water-absorbing ability, gel hardness after water absorption, etc. changed as appropriate depending on the amounts of the reducing agent and oxidizing agent used. In the general formula, for example,
When the amount of reducing agent used is changed while the amount of oxidizing agent added is constant, the tendency to solubilize increases beyond a certain range in which the water absorption capacity increases as the amount of reducing agent used increases. Furthermore, when the amount of the oxidizing agent used is increased while the amount of the reducing agent used is constant, the amount of water absorbed decreases and the gel state after water absorption becomes hard, whereas when the amount is decreased, the gel state tends to become soft. However, when each is used in a proportionately increased or decreased amount within the above-mentioned addition range, no significant difference is observed in the performance of the resulting polymers.
また、この発明の製造方法において、硝酸アル
ミニウム、酢酸アルミニウム、塩化アルミニウ
ム、硫酸アルミニウム等のアルミニウム塩、アル
ミニウムアルコラート、アルミン酸ナトリウム等
のアルミン酸塩等のアルミニウム化合物を添加す
ることにより、重合体の架橋度を調整することも
できる。特に触媒濃度が低い条件下で製造された
吸水性樹脂は、可溶性部分を含有したり吸水後の
ゲル状態が軟らかくなる傾向があるので、このよ
うな場合に上記アルミニウム化合物を添加する
と、吸水量の増加およびゲル強度の改良を図るこ
とができる。なお、上記アルミニウム化合物中、
アルミニウム塩等はモノマー水溶液または触媒水
溶液のいずれに添加しても使用できるが、アルミ
ン酸塩の場合には、触媒水溶液に添加するとアル
カリが触媒を分解する恐れがあるので、モノマー
水溶液中に添加するのがよい。これらのアルミニ
ウム化合物は、通常、モノマー仕込み量100重量
部に対して5重量部以下、好ましくは0.1〜0.5重
量部程度添加される。 Furthermore, in the production method of the present invention, by adding aluminum compounds such as aluminum salts such as aluminum nitrate, aluminum acetate, aluminum chloride, and aluminum sulfate, and aluminates such as aluminum alcoholate and sodium aluminate, the polymer can be crosslinked. You can also adjust the degree. In particular, water-absorbent resins produced under conditions with low catalyst concentration tend to contain soluble portions or become soft after water absorption, so adding the above aluminum compound in such cases will reduce the amount of water absorbed. It is possible to increase the gel strength and improve the gel strength. In addition, in the above aluminum compound,
Aluminum salts, etc. can be used by adding them to either the monomer aqueous solution or the catalyst aqueous solution, but in the case of aluminates, adding them to the catalyst aqueous solution may cause the alkali to decompose the catalyst, so they should be added to the monomer aqueous solution. It is better. These aluminum compounds are usually added in an amount of 5 parts by weight or less, preferably about 0.1 to 0.5 parts by weight, per 100 parts by weight of the monomer.
次に、この発明の製造方法の一例を詳細に説明
する。 Next, an example of the manufacturing method of the present invention will be explained in detail.
まず、アクリル酸を前記の中和剤水溶液にて所
望の中和度および重合に適当な濃度となるように
中和する。この溶液に前記の還元剤水溶液を添加
し重合を開始する。重合の進行と共に該溶液は粘
度が上昇し、ある程度重合が進行し高粘度となつ
た時、前記の酸化剤水溶液を反応系に添加して、
必要に応じて加熱し、処理した後、反応液を脱水
乾燥させて、この発明の吸水性樹脂が得られる。 First, acrylic acid is neutralized with the neutralizing agent aqueous solution to a desired degree of neutralization and a concentration suitable for polymerization. The aforementioned reducing agent aqueous solution is added to this solution to initiate polymerization. As the polymerization progresses, the viscosity of the solution increases, and when the polymerization progresses to a certain extent and the viscosity becomes high, the oxidizing agent aqueous solution is added to the reaction system,
After heating and processing as necessary, the reaction solution is dehydrated and dried to obtain the water absorbent resin of the present invention.
上記の工程において、還元剤による重合は通常
室温で充分に進行するが、必要に応じて加温また
は加熱してもよい。加温または加熱した場合に
は、重合反応は速やかに進行し、粘度は急激に上
昇するので、酸化剤の添加時期は重要であり、得
られた樹脂の吸水能力に大きく影響する。一般的
な傾向として、酸化剤の添加時期が遅れると、高
粘度のため、添加された酸化剤の均質な分散が妨
げられ、重合物が不均質なものとなり、可溶性の
部分が生ずる恐れがある。従つて、加温または加
熱する場合には、アリルアルコール、プロピレン
グリコール等の重合遅延剤の併用が好ましい。 In the above steps, polymerization using a reducing agent usually proceeds sufficiently at room temperature, but heating or heating may be performed as necessary. When heated or heated, the polymerization reaction proceeds rapidly and the viscosity rapidly increases, so the timing of addition of the oxidizing agent is important and greatly affects the water absorption ability of the resulting resin. As a general tendency, if the oxidizing agent is added late, the high viscosity will prevent the added oxidizing agent from homogeneous dispersion, resulting in a non-homogeneous polymer, which may result in soluble portions. . Therefore, when warming or heating, it is preferable to use a polymerization retarder such as allyl alcohol or propylene glycol in combination.
酸化剤添加後の処理温度は、使用する酸化剤が
分解または活性化する温度ないしそれ以上の温度
でよい。酸化剤による処理後反応系内の水分を除
去し乾燥すること、また100℃程度で酸化剤処理
をしても性能その他に何等変化が認められなかつ
たことなどを考慮すると系内に共存する水分の沸
点程度で処理するのが好都合である。 The treatment temperature after adding the oxidizing agent may be at or above the temperature at which the oxidizing agent used is decomposed or activated. Considering the fact that moisture in the reaction system must be removed and dried after treatment with an oxidizing agent, and that no change in performance or other properties was observed even after treatment with an oxidizing agent at around 100°C, moisture coexisting in the system can be reduced. It is convenient to process at around the boiling point of .
<作用>
この発明は上記の構成よりなり、従来の過硫酸
塩やレドツクス開始剤による重合と異なり、含硫
黄系還元剤によるアクリル酸類の重合は極めて発
熱性が低く、温和な条件下に速やかに進行し、あ
る程度重合が進行した後酸化剤により処理し、さ
らなる重合または架橋反応をするので、重合中に
おける温度制御が容易となり、暴走反応等を防止
できる。<Function> The present invention has the above-mentioned structure, and unlike the conventional polymerization using persulfates or redox initiators, the polymerization of acrylic acids using a sulfur-containing reducing agent has extremely low heat generation and can be carried out quickly under mild conditions. After the polymerization has progressed to a certain extent, it is treated with an oxidizing agent and further polymerization or crosslinking reaction is carried out, which makes it easy to control the temperature during polymerization and prevent runaway reactions.
また、重合が温和な条件下に進行するので、副
反応等が少なく、吸水能力の大きな吸水性樹脂を
得ることができる。 Furthermore, since the polymerization proceeds under mild conditions, there are few side reactions, etc., and a water-absorbing resin with high water-absorbing capacity can be obtained.
<実施例>
以下、実施例をもつて、この発明をより詳細に
説明する。<Examples> The present invention will be described in more detail below with reference to Examples.
実施例 1
アクリル酸10gを25%濃度の水酸化ナトリウム
水溶液20gで中和し、常温で1.0%濃度のピロ亜
硫酸カリウム水溶液1gを加えると、約5分間で
重合して攪拌可能な粘性体が得られる。この重合
時の系内の温度は35℃乃至45℃であり、モノマー
溶液の量を増加してもこの温度は余り変化しな
い。得られた粘性体は数時間以上経過すると経時
的に固体と液体に分離する傾向にあるが、分離以
前の状態ではチキソトロピツク性があり、攪拌で
水様の低粘性液となるので、この状態で1%濃度
のペルオキソニ硫酸カリウム水溶液1gを加える
と、均質な溶液が得られるが、このものを60℃以
上に加熱すると数分後にタツク性のないゴム状重
合体となる。この場合の加熱温度が高ければ処理
時間は短くなるが、発熱や突沸現象は認められな
いし、処理温度による吸水性能の相違も認められ
なかつた。得られた重合体を脱水乾燥したもの
は、水道水で約1000倍、0.9%食塩水で約100倍の
吸水性能を示した。Example 1 When 10 g of acrylic acid is neutralized with 20 g of a 25% sodium hydroxide aqueous solution and 1 g of a 1.0% potassium pyrosulfite aqueous solution is added at room temperature, it polymerizes in about 5 minutes to obtain a stirrable viscous material. It will be done. The temperature within the system during this polymerization is 35°C to 45°C, and this temperature does not change much even if the amount of monomer solution is increased. The obtained viscous substance tends to separate into solid and liquid over time after several hours, but before separation it has thixotropic properties and becomes a water-like low viscosity liquid when stirred, so it cannot be used in this state. When 1 g of a 1% potassium peroxodisulfate aqueous solution is added, a homogeneous solution is obtained, but when this solution is heated above 60° C., it becomes a rubbery polymer with no tackiness after a few minutes. In this case, if the heating temperature is high, the treatment time will be shortened, but no heat generation or bumping phenomenon was observed, and no difference in water absorption performance depending on the treatment temperature was observed. The resulting polymer, which was dehydrated and dried, exhibited water absorption performance that was approximately 1000 times greater in tap water and approximately 100 times greater in 0.9% saline.
実施例 2
アクリル酸10gに25%濃度の水酸化ナトリウム
水溶液20gを加えて中和したものを、60℃以上に
加熱混合できるミキサー中に、1%濃度のピロ亜
硫酸カリウム水溶液3gと共に加熱混合攪拌しな
がら投入し、重合が充分に完了する前に1%濃度
のペルオキソニ硫酸カリウム水溶液1gを加え、
加熱混合攪拌を継続する。その後、脱水乾燥して
重合物を得る。得られた重合物の吸水性能は実施
例1のものと同様であつた。Example 2 10 g of acrylic acid was neutralized by adding 20 g of a 25% sodium hydroxide aqueous solution, and the mixture was heated and stirred with 3 g of a 1% potassium pyrosulfite aqueous solution in a mixer that can be heated to 60°C or higher. Before the polymerization was sufficiently completed, 1 g of a 1% potassium peroxodisulfate aqueous solution was added.
Continue heating, mixing and stirring. Thereafter, it is dehydrated and dried to obtain a polymer. The water absorption performance of the obtained polymer was similar to that of Example 1.
実施例 3
アクリル酸10gに25%濃度の水酸化ナトリウム
水溶液20gを加えて中和したものにアクリルアミ
ド0.3gを溶解し、常温(約30℃)で2%濃度の
亜ニチオン酸ナトリウム水溶液1.5gを添加する
とただちに重合が開始し若干の発熱とともに粘度
が上昇する。1分30秒後にさらにペルオキソ二硫
酸カリウムと硝酸アルミニウム9水塩を各々2%
溶解した水溶液2gを加えて混合すると、粘度が
さらに上昇し数分以内にゴム状を呈するが、これ
を60℃以上に加熱乾燥して得られたものは、0.9
%食塩水中約100倍の吸水性能を示した。Example 3 10 g of acrylic acid was neutralized by adding 20 g of a 25% aqueous sodium hydroxide solution, 0.3 g of acrylamide was dissolved, and 1.5 g of a 2% aqueous sodium dithionite solution was added at room temperature (approximately 30°C). Upon addition, polymerization begins immediately and the viscosity increases with slight heat generation. After 1 minute and 30 seconds, add 2% each of potassium peroxodisulfate and aluminum nitrate nonahydrate.
When 2 g of the dissolved aqueous solution is added and mixed, the viscosity increases further and becomes rubbery within a few minutes, but the product obtained by heating and drying this at 60°C or higher has a viscosity of 0.9
% saline solution.
上記実施例中、亜二チオン酸ナトリウム水溶液
およびペルオキソ二硫酸カリウムと硝酸アルミニ
ウム9水塩との混合水溶液の濃度を1%とし、そ
れぞれの添加量を3gおよび2gとして、同様に
吸水性樹脂を製造した。得られた吸水性樹脂は、
0.9%食塩水中150〜170倍の吸水性能を示し、給
水後のゲルはやや軟らかいが可溶性部分はなかつ
た。 In the above example, the concentration of the sodium dithionite aqueous solution and the mixed aqueous solution of potassium peroxodisulfate and aluminum nitrate nonahydrate was set to 1%, and the amounts added were set to 3 g and 2 g, respectively, and water absorbent resins were produced in the same manner. did. The obtained water absorbent resin is
It exhibited 150 to 170 times the water absorption performance of 0.9% saline, and the gel after water supply was slightly soft, but there was no soluble portion.
<効果>
以上のように、この発明の吸水性樹脂の製造方
法によれば、特殊の重合開始剤を使用することに
より温和な条件下に重合が進行し、温度制御が容
易になるので、安全かつ広い範囲で重合条件を設
定できる。また、技術的、装置的に容易かつ簡易
であり、安全性および経済性にも優れる。得られ
る吸水性樹脂も、その吸水性能に優れるととも
に、使用される還元剤および酸化剤の量を適宜変
更することにより、その性状および性能を変更で
き、所望の製品がえられ、その適用範囲を拡大す
ることができる。さらに、その製法においても、
公知のものを含め幅広い方法を利用でき、例え
ば、回転移動するベルト上に連続的にモノマー溶
液を均一に流しこめば、フイルムまたは板状物が
得られるし、上下に回転する加熱板や加熱した不
活性気体または空気中に噴霧すれば粉末状にする
ことができる。また、形状物や不織布等への塗布
含浸後の加熱や、ロールやスクリユー或いはミキ
サー中での混練加熱、さらには溶媒の沸点を利用
して脱水粉末状にする逆相乳化重合法等、種々の
製造方法を利用することができるという利点を有
する。<Effects> As described above, according to the method for producing a water-absorbent resin of the present invention, polymerization proceeds under mild conditions by using a special polymerization initiator, and temperature control is facilitated, resulting in safety. Moreover, polymerization conditions can be set within a wide range. In addition, it is technically and equipment-wise easy and simple, and has excellent safety and economical efficiency. The resulting water-absorbing resin has excellent water-absorbing performance, and its properties and performance can be changed by appropriately changing the amounts of the reducing agent and oxidizing agent used, making it possible to obtain the desired product and expand its application range. Can be expanded. Furthermore, in its manufacturing method,
A wide variety of methods can be used, including those known in the art. It can be made into a powder by spraying into an inert gas or air. In addition, there are various methods such as heating after coating and impregnating shaped objects and non-woven fabrics, kneading and heating in rolls, screws, or mixers, and inverse emulsion polymerization to dehydrate powder using the boiling point of the solvent. It has the advantage that the manufacturing method can be used.
Claims (1)
未満のアクリル酸を含硫黄系還元剤で重合した
後、酸化剤を添加し処理することを特徴とする吸
水性樹脂の製造方法。 2 含硫黄系還元剤が、亜硫酸塩、亜硫酸水素
塩、チオ硫酸塩または亜二チオン酸塩である上記
特許請求の範囲第1項記載の吸水性樹脂の製造方
法。 3 酸化剤がペルオキソ二硫酸塩である上記特許
請求の範囲第1項記載の吸水性樹脂の製造方法。[Claims] 1. Degree of neutralization by monovalent cations is 30% or more and 100%.
1. A method for producing a water-absorbing resin, which comprises polymerizing acrylic acid with a sulfur-containing reducing agent and then adding an oxidizing agent. 2. The method for producing a water-absorbing resin according to claim 1, wherein the sulfur-containing reducing agent is a sulfite, a hydrogen sulfite, a thiosulfate, or a dithionite. 3. The method for producing a water-absorbing resin according to claim 1, wherein the oxidizing agent is peroxodisulfate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8137086A JPS62236807A (en) | 1986-04-09 | 1986-04-09 | Production of water-absorptive resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8137086A JPS62236807A (en) | 1986-04-09 | 1986-04-09 | Production of water-absorptive resin |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62236807A JPS62236807A (en) | 1987-10-16 |
JPH0476362B2 true JPH0476362B2 (en) | 1992-12-03 |
Family
ID=13744424
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8137086A Granted JPS62236807A (en) | 1986-04-09 | 1986-04-09 | Production of water-absorptive resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62236807A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10015135A1 (en) | 2000-03-29 | 2001-10-04 | Basf Ag | Process for modifying polymers containing acid groups |
DE102005042038A1 (en) * | 2005-09-02 | 2007-03-08 | Basf Ag | Process for the preparation of water-absorbing polymers |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5849714A (en) * | 1981-09-18 | 1983-03-24 | Arakawa Chem Ind Co Ltd | Preparation for dried solid of polyacrylic acid salt |
-
1986
- 1986-04-09 JP JP8137086A patent/JPS62236807A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5849714A (en) * | 1981-09-18 | 1983-03-24 | Arakawa Chem Ind Co Ltd | Preparation for dried solid of polyacrylic acid salt |
Also Published As
Publication number | Publication date |
---|---|
JPS62236807A (en) | 1987-10-16 |
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Legal Events
Date | Code | Title | Description |
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LAPS | Cancellation because of no payment of annual fees |