JPH02178332A - Method for antistatic treatment of water absorbing resin powder - Google Patents
Method for antistatic treatment of water absorbing resin powderInfo
- Publication number
- JPH02178332A JPH02178332A JP63331835A JP33183588A JPH02178332A JP H02178332 A JPH02178332 A JP H02178332A JP 63331835 A JP63331835 A JP 63331835A JP 33183588 A JP33183588 A JP 33183588A JP H02178332 A JPH02178332 A JP H02178332A
- Authority
- JP
- Japan
- Prior art keywords
- water
- resin powder
- absorbing resin
- antistatic treatment
- powder
- 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
- 239000000843 powder Substances 0.000 title claims abstract description 46
- 239000011347 resin Substances 0.000 title claims abstract description 42
- 229920005989 resin Polymers 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 title claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract description 18
- 150000002484 inorganic compounds Chemical class 0.000 claims abstract description 14
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 14
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 6
- 239000011701 zinc Substances 0.000 claims abstract description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000011575 calcium Substances 0.000 claims abstract description 3
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 3
- 239000000470 constituent Substances 0.000 claims abstract description 3
- 230000002265 prevention Effects 0.000 claims description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 8
- 230000000694 effects Effects 0.000 abstract description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 3
- 239000000017 hydrogel Substances 0.000 abstract description 3
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 2
- 150000001340 alkali metals Chemical class 0.000 abstract description 2
- 229920006037 cross link polymer Polymers 0.000 abstract description 2
- 230000008961 swelling Effects 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 235000004416 zinc carbonate Nutrition 0.000 description 7
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 6
- 239000002250 absorbent Substances 0.000 description 6
- 230000003068 static effect Effects 0.000 description 6
- 239000011667 zinc carbonate Substances 0.000 description 6
- 229910000010 zinc carbonate Inorganic materials 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- 230000002745 absorbent Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000010216 calcium carbonate Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000203 mixture Substances 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
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】 〈産業上の利用分野〉 本発明は吸水性樹脂粉末の帯電防止処理法に関する。[Detailed description of the invention] <Industrial application field> The present invention relates to a method for antistatic treatment of water-absorbing resin powder.
〈従来の技術〉
吸水性樹脂粉末は、優れた吸水能力および多少の圧力を
受けても一度吸水した液は離水しないという優れた保持
ツノから、バルブや吸水紙に代わる液吸収素材として、
おむつ、生理用品等の衛生用品メーカーを中心に注目を
集め実用化されてきたものであり、近年、その用途は農
業、園芸、食品、メディカル等に幅広く拡がりつつある
。<Prior art> Water-absorbing resin powder has been used as a liquid-absorbing material to replace valves and water-absorbing paper due to its excellent water-absorbing ability and excellent retention horns that prevent liquid from separating once absorbed even when subjected to some pressure.
It has attracted attention and been put into practical use mainly by manufacturers of sanitary products such as diapers and sanitary products, and in recent years, its uses have been expanding widely to agriculture, horticulture, food, medical, etc.
ところで、吸水性樹脂粉末は親水性ではあっても、本来
、非導電性物質であるため、粉末同士の摩擦により静電
気を蓄積して帯電しやすい性質を白−している。Incidentally, although water-absorbing resin powder is hydrophilic, it is originally a non-conductive substance, so it has a tendency to accumulate static electricity due to friction between the powders and become electrically charged.
このため、帯電した場合、吸水性樹脂の製造工程におい
てその中間品または最終仕上品を空気輸送する際に、帯
電による粉塵爆発を引き起こす危険性があった。For this reason, when charged, there is a risk of causing a dust explosion due to the charging when an intermediate product or a final finished product is air-transported in the manufacturing process of water-absorbent resin.
また、吸水性樹脂粉末は、通常、防湿性のプラスチック
フィルム製の内貸を有する紙袋に15〜20 kq小単
位包装・出荷されているが、吸水性樹脂粉末が帯電した
場合、内貸にかなりの量の吸水性樹脂粉末が付着するた
め、包装内の吸水性樹脂粉末を余すことなく使用するこ
とができないという不経済があった。In addition, water-absorbing resin powder is usually packaged and shipped in small units of 15 to 20 kq in paper bags with inner walls made of moisture-proof plastic film. Since this amount of water-absorbing resin powder adheres to the package, there is an uneconomical situation in that the water-absorbing resin powder in the package cannot be used completely.
さらに、吸水性樹脂粉末を用いて、おむつ、生理用品等
を製造する場合においても、帯電によって生した静゛i
は気が放電して装置か損傷したり、塵やほこりか付着し
たりして火災か発生ずる等、種々の設備上のトラブルが
発生する虞があった。Furthermore, even when manufacturing diapers, sanitary products, etc. using water-absorbing resin powder, the static i
There was a risk that various equipment troubles could occur, such as air discharge and damage to the equipment, or dust and dust adhering to it, which could cause a fire or other problems.
かかる吸水性樹脂粉末が静7b気を蓄積するのを防止す
るための帯電防止処理法としては、従来、界面活性剤を
用いる処理法か一般に用いられてきた。この界面活性剤
を用いる処理法は、帯電防止能を白゛する界面活性剤を
吸水性樹脂の内部に練り込んだり、外部に塗(Iiシた
りして、静電気の蓄積をμJ+I−する処理法である。Conventionally, a treatment method using a surfactant has been generally used as an antistatic treatment method for preventing the water-absorbing resin powder from accumulating static air. This treatment method using a surfactant is a treatment method in which a surfactant with antistatic ability is kneaded into the interior of the water-absorbing resin or coated on the outside (Ii) to reduce the accumulation of static electricity. It is.
〈発明が解決しようどする課題〉
しかしながら、上記従来の帯電防止処理法は、−時的な
除電法であるため、永久的な帯電防止処理を期待できな
いとともに、界面活性剤が一般に油状であるため、吸水
性樹脂粉末に付着させて界面活性剤層を形成させた場合
、べとつきにより粉体流動性が低下して作業性が悪くな
るという問題があった。<Problems to be Solved by the Invention> However, the above-mentioned conventional antistatic treatment method is a temporary static elimination method, so permanent antistatic treatment cannot be expected, and the surfactant is generally oily. When a surfactant layer is formed by adhering it to a water-absorbing resin powder, there is a problem that the powder fluidity decreases due to stickiness, resulting in poor workability.
本発明は以上の事情に鑑みなされたものであって、その
目的とするところは、優れた処理効果を有するとともに
、処理後も優れた粉体流動性を有し、作業性が低下する
ことのない吸水性樹脂粉末の帯7ヒ防止処理法を提供す
るにある。The present invention has been made in view of the above circumstances, and its purpose is to have excellent processing effects, as well as excellent powder flowability even after processing, and to prevent the decrease in workability. To provide a method of treating water-absorbing resin powder to prevent damage.
く課題を解決するだめの手段〉
上記Ll的を達成するための本発明に係る吸水性樹脂粉
末の帯電防止処理法(以下、「本発明方法」という)に
おいては、吸水性樹脂粉末に、所定の無機化合物の粉末
を、該吸水性樹脂粉末100重量部に対して、0.01
〜5重量部添加する。Means for Solving the Problem> In the method for antistatic treatment of water-absorbing resin powder according to the present invention (hereinafter referred to as the "method of the present invention") to achieve the above-mentioned object, a predetermined amount is added to the water-absorbing resin powder. 0.01 parts by weight of the inorganic compound powder per 100 parts by weight of the water-absorbing resin powder.
Add up to 5 parts by weight.
本発明方法において用いられる無機化合物の粉末は、亜
鉛またはカルシウムを構成元素として何する無機化合物
の粉末である。The inorganic compound powder used in the method of the present invention is an inorganic compound powder containing zinc or calcium as a constituent element.
以下、本発明方法を詳細に説明する。The method of the present invention will be explained in detail below.
本発明方法を用いて帯電防止処理しiGる粉末状の吸水
性樹脂としては、水に溶解せず、水中において自重の5
0倍程度以上の水を吸収して膨潤し、ヒドロゲルを形成
する樹脂であればよく、例えばアクリル酸のアルカリ金
属による部分的中和物の重合体架橋物、澱粉−アクリロ
ニトリルクラフト重合体の加水分解物、澱粉−アクリル
酸グラフトifi合体の中和物、架橋カルボキンメチル
セルロス、アクリル酸メチル−酢酸ビニル共重合体の加
水分解物、架橋ポリビニルアルコール変成物などが挙げ
られる。The powdered water-absorbing resin treated with antistatic treatment using the method of the present invention does not dissolve in water and has a weight of 50% of its own weight in water.
Any resin that absorbs about 0 times more water, swells, and forms a hydrogel may be used, such as crosslinked polymers of partially neutralized acrylic acid with alkali metals, hydrolysis of starch-acrylonitrile craft polymers, etc. Examples include neutralized products of starch-acrylic acid graft ifi combination, cross-linked carboxyne methyl cellulose, hydrolyzed products of methyl acrylate-vinyl acetate copolymers, and modified products of cross-linked polyvinyl alcohol.
本発明方法は、粉末状の吸水性樹脂の帯電防止処理に適
用される。処理対象の粉末の大きさは、通常10〜20
0メツシユであり、これらの粉末同士の摩擦により帯電
しやすいものである。なお、上記粒度範囲のものを用い
るのは、10メソンユ未満の場合、吸水速度が小さくな
るからであり、200メツシユを越えた場合、ままこ現
象が生じるからである。The method of the present invention is applied to antistatic treatment of powdered water absorbent resin. The size of the powder to be treated is usually 10 to 20
0 mesh, and is easily charged due to friction between these powders. The reason for using the particle size within the above range is that if the particle size is less than 10 mesh, the water absorption rate will be low, and if it exceeds 200 mesh, a sticky phenomenon will occur.
本発明方法において用いられる無機化合物としては、具
体的には、亜鉛華、炭酸亜鉛などの亜鉛の酸化物または
炭酸塩、炭酸カルシウム、酸化カルシウム、硫酸カルシ
ウム、水酸化カルシウムなどのカルシウムの炭酸塩、酸
化物、硫酸塩または水酸化物が例示される。Specifically, the inorganic compounds used in the method of the present invention include zinc oxides or carbonates such as zinc white and zinc carbonate, calcium carbonates such as calcium carbonate, calcium oxide, calcium sulfate, and calcium hydroxide; Examples include oxides, sulfates, and hydroxides.
また、用いる無機化合物は、含水物か無水物かを限定さ
れず、また含水物の含水量もまた限定されない。Furthermore, the inorganic compound used is not limited to whether it is a hydrated compound or an anhydrous compound, and the water content of the hydrated compound is also not limited.
なお、上記無機化心物は、一種または二種以上の粉末を
混合して用いてよい。In addition, the above-mentioned mineralized core may be used alone or in combination of two or more powders.
上記無機化合物の粒径は、小さい方が本発明方法を実施
する上で適しており、平均粒径50μm以下のものが好
ましい。平均粒径か50μmを越えた場合、吸水性樹脂
粉末から無機化合物か分離して好ましくないからである
。The smaller the particle size of the above-mentioned inorganic compound, the more suitable it is for carrying out the method of the present invention, and the average particle size is preferably 50 μm or less. This is because if the average particle size exceeds 50 μm, the inorganic compound will separate from the water-absorbing resin powder, which is undesirable.
本発明方法においては、粉末状の上記無機化合物を、吸
水性樹脂粉末100重量部に対して、0.01〜5重量
部用いる必要がある。このように添加口を限定したのは
、0,01重口部未満の場合、帯電防止のための有意な
添加効果が期待できないからであり、5重量部を越えた
場合、増mに相応した添加効果が得られないのみならす
、飛散の問題が生じるからである。In the method of the present invention, it is necessary to use 0.01 to 5 parts by weight of the above-mentioned powdered inorganic compound based on 100 parts by weight of the water-absorbing resin powder. The reason why the addition port was limited in this way is that if the amount is less than 0.01 parts by weight, no significant effect for preventing static electricity can be expected. This is because not only the effect of addition cannot be obtained, but also the problem of scattering occurs.
吸水性樹脂粉末と上記無機化合物とを混合することによ
り、該吸水性樹脂に帯電防止処理か施される。By mixing the water-absorbing resin powder and the above-mentioned inorganic compound, the water-absorbing resin is subjected to antistatic treatment.
混合方法としては、従来公知の種々の方法を用いること
ができ、例えばタンブラ−Vブレンダスーパーミキサー
ナウターミキサ−リボンブレンダー コニカルブレン
ダ−、ヘンシェルミキサー レディゲミキサーなどの種
々の混合機を用いて混合することができる。As a mixing method, various conventionally known methods can be used. For example, mixing can be performed using various mixers such as a tumbler-V blender super mixer, a Nauta mixer-ribbon blender, a conical blender, a Henschel mixer, a Loedige mixer, etc. can.
無機化合物の粉末が、吸水性樹脂粉末から分離するのを
防止するために、両者を混合する前に、吸水性樹脂粉末
の吸水性能に悪影響を与えない程度の二および種類の展
着剤を混合して粉末の表面にコーティングしてもよい。In order to prevent the inorganic compound powder from separating from the water-absorbing resin powder, two types of spreading agents are mixed before mixing the two to an extent that does not adversely affect the water-absorbing performance of the water-absorbing resin powder. The surface of the powder may be coated.
コーティングに用い得る展右剤としては、液状ポリブテ
ン、液状ポリエチレングリコール、多価アルコール、グ
リコールエーテル化合物などが挙げられる。Examples of spreading agents that can be used for coating include liquid polybutene, liquid polyethylene glycol, polyhydric alcohol, and glycol ether compounds.
〈実施例〉 以下、本発明を実施例に基いて、より詳細に説明する。<Example> Hereinafter, the present invention will be explained in more detail based on Examples.
なお、本発明方法は、下記の実施例に示す処理法に限定
されるものではな(、本発明の要旨を変更しない範囲で
、適宜変更を加え得ることは勿論である。It should be noted that the method of the present invention is not limited to the processing method shown in the following examples (it goes without saying that changes may be made as appropriate without changing the gist of the present invention.
(A)吸水性樹脂粉末の調製
80%アクリル酸75重量部、48.6%水酸化ナトリ
ウム48.0重量部およびイオン交換水48.6重量部
を混合して中和度70%のアクリル酸塩水溶液を調製し
た。このアクリル酸塩水溶液1028gに、1%N、N
−メチレンビスアクリルアミド水溶液5gを添加して窒
素置換した後、2%ベルオキソニ硫酸塩に2 S2 o
s水溶液36g、2%ピロ亜硫酸塩に2 S205水溶
液21.6gおよび40%グリオキサール水溶液を水で
50倍に薄めた希釈液14.4gを添加して混合液を得
た。次いで、この混合液を、縦48cm。(A) Preparation of water absorbent resin powder 75 parts by weight of 80% acrylic acid, 48.0 parts by weight of 48.6% sodium hydroxide and 48.6 parts by weight of ion-exchanged water were mixed to obtain acrylic acid with a degree of neutralization of 70%. An aqueous salt solution was prepared. To 1028 g of this acrylate aqueous solution, add 1% N, N
- After adding 5 g of methylene bisacrylamide aqueous solution and purging with nitrogen, 2 S2 o
A mixed solution was obtained by adding 21.6 g of 2S205 aqueous solution and 14.4 g of a diluted solution of 40% glyoxal aqueous solution diluted 50 times with water to 36 g of S205 aqueous solution and 2% pyrosulfite. Next, spread this mixture into a length of 48 cm.
横37 crnのバット(内面テフロンコーティング)
に注入し、乾燥温度42℃の熱風循環乾燥器内で20分
間重合して縦48 cm、横37cm、厚さ5〜6 m
mの板状の含水ゲルを得た。得られた含水ゲルを表面温
度130℃のドラムドライヤで乾燥してフレーク状の樹
脂とし、この樹脂をピンミルで粉砕した後、分級し、6
0〜120メツシユの吸水性樹脂粉末を得た。Width 37 crn butt (inner Teflon coating)
and polymerized for 20 minutes in a hot air circulation dryer at a drying temperature of 42°C to form a product with a length of 48 cm, a width of 37 cm, and a thickness of 5 to 6 m.
A plate-shaped hydrogel of m was obtained. The obtained hydrous gel was dried with a drum dryer at a surface temperature of 130°C to obtain a flaky resin, which was crushed with a pin mill and then classified.
A water absorbent resin powder having a mesh size of 0 to 120 was obtained.
上記吸水性樹脂粉末を、温度22℃、相対湿度60%の
恒温・恒湿室内の、シリカゲルを収容したデシケータ−
内で一昼夜乾燥した。The above water absorbent resin powder was placed in a desiccator containing silica gel in a constant temperature and humidity chamber at a temperature of 22°C and a relative humidity of 60%.
It was left to dry inside for a day and a night.
(B)吸水性樹脂粉末の帯電防止処理
(実施fll 1 )
上記(A)で得た吸水性樹脂粉末100gと、無機化合
物としての粉末状の炭酸亜鉛(正同化学社製)0.5g
とを、前記恒温・恒湿室内で、小型撹拌機にて均一に攪
拌混合することにより、帯電防止処理を行ない試料1を
得た。(B) Antistatic treatment of water-absorbing resin powder (implementation full 1) 100 g of water-absorbing resin powder obtained in (A) above and 0.5 g of powdered zinc carbonate (manufactured by Seido Kagaku Co., Ltd.) as an inorganic compound.
Sample 1 was obtained by uniformly stirring and mixing with a small stirrer in the above-mentioned constant temperature and constant humidity room to perform antistatic treatment.
(実施例2)
炭酸亜鉛に代えて、亜鉛華1号(堺化学工業社製)を同
量用いたこと以外は実施例1と同様にして、帯電防止処
理を行い試料2を得た。(Example 2) Sample 2 was obtained by antistatic treatment in the same manner as in Example 1, except that the same amount of Zinc Flower No. 1 (manufactured by Sakai Chemical Industry Co., Ltd.) was used in place of zinc carbonate.
(実施例3)
炭酸亜鉛に代えて、軽質の炭酸カルシウム(竹原化学工
業社製)を同量用いたこと以外は実施例1と同様にして
、帯電防止処理を行い試料3を得た。(Example 3) Sample 3 was obtained by antistatic treatment in the same manner as in Example 1 except that the same amount of light calcium carbonate (manufactured by Takehara Chemical Industry Co., Ltd.) was used in place of zinc carbonate.
(比較例1)
帯電防止処理を行わなかった吸水性樹脂粉末を比較試料
1とした。(Comparative Example 1) Comparative Sample 1 was a water-absorbing resin powder that was not subjected to antistatic treatment.
(比較例2)
炭酸亜鉛に代えて、タルク(竹原化学工業社製)を同量
用いたこと以外は実施例1と同様にして、帯電防止処理
を行い比較試料2を得た。(Comparative Example 2) Comparative Sample 2 was obtained by performing antistatic treatment in the same manner as in Example 1, except that the same amount of talc (manufactured by Takehara Chemical Industry Co., Ltd.) was used instead of zinc carbonate.
(比較例3)
炭酸亜鉛に代えて、シリカ(東洋曹達社製、商品名「ト
クシール」)を同量用いたこと以外は実施例1と同様に
して、帯電防止処理を行い比較試料3を得た。(Comparative Example 3) Comparative sample 3 was obtained by carrying out antistatic treatment in the same manner as in Example 1 except that the same amount of silica (manufactured by Toyo Soda Co., Ltd., trade name "Tokusil") was used instead of zinc carbonate. Ta.
(C)帯電防止能の評価試験
上記試料1〜3および比較試料1〜3から各10gを分
取して、内面が厚さ0.03mm、縦100mm、横1
50 mmのポリエチレン製フィルムでできている袋に
入れ、袋の開口部を手で絞って閉じた後、袋を30秒間
強く手で上下左右に振って、吸水性樹脂粉末のフィルム
への付着状態を目視にて観察し、各試料または比較試料
についての帯電防止能を下記の基準で評価した。(C) Evaluation test for antistatic ability Take 10 g of each sample from Samples 1 to 3 and Comparative Samples 1 to 3, and measure the inner surface with a thickness of 0.03 mm, a length of 100 mm, and a width of 1 mm.
Place it in a bag made of 50 mm polyethylene film, squeeze the opening of the bag with your hands to close it, and then shake the bag strongly by hand for 30 seconds to see how the water-absorbing resin powder adheres to the film. was visually observed, and the antistatic ability of each sample or comparative sample was evaluated using the following criteria.
(評価基■) 1rt’ fjlIi A 計 fllti B − 計fdfi C 1ニド 11tli l:) F II己 ノン に 、 仝 く イ・I’ iji l、 f塚 い 。(Evaluation basis ■) 1rt' fjlIi A Total flti B - Total FDFI C 1nido 11tli l:) F II Non ni I, I', I, I.
少1−2イ・11:、−するたけ゛である。Elementary 1-2 A.11: - It's all you need to do.
・かなりイーj青する。・It's pretty blue.
・・はとんと仝而に付i5−する。・I'll attach it to you.
上1;己1汁 4Hi W古 里 を jくず。Top 1; Self 1 soup 4 Hi W Kosato j scraps.
表 −2だ。table -2.
以−1,より、従来公知のHF ’i(S Vl、l上
処理7ノニに比べて、本発明り法は優、f−iた:j:
′:1i防止り1理法であることが分った。From the above-1, compared to the conventionally known HF'i (S Vl, l top treatment), the method of the present invention has superior f-i:j:
': It turns out that there is only one principle to prevent 1i.
<発明の効果〉
以上説明し、たように、本発明に係る吸水性樹脂粉末の
帯電防1ト処理法は、優れたー:”+”t m Ui
tL Q、処理を可能にする等、本発明は優れた持白°
の効果を奏す十1己友に・j(すよ5に、+で老明力l
去を](1いて↑(′iijiJ、111シ1ル理した
吸水性樹脂粉末(試料1〜3)は、−y73;エチlノ
:、製−フイルj2に全く付Is l−7ないか、少し
イ・I’6したのに過ぎないのに21し2て、::)重
両1ト処理をi)tつなか、−ンたもの(比較試料1)
および本宅1111ツノ7、!、によ・:3ないて:;
′f屯防止処理を行、−〕だしの(比較試す−12およ
び3)は、付着の程度が激しか代
理 人<Effects of the Invention> As explained above and as mentioned above, the antistatic treatment method for water-absorbing resin powder according to the present invention has excellent results.
The present invention has excellent whitening properties, such as enabling tLQ and processing.
To the 11th self-friend with the effect of ・j
The water-absorbent resin powder (samples 1 to 3) treated with 111 sheets was not attached at all to the film j2 made by -y73; , even though it was only a little I'6, it was 21 and 2 ::) Heavy and double processing was done i)t, - (comparative sample 1)
and Hontaku 1111 Tsuno 7,! , yo・:3 naite:;
``Fun prevention treatment is carried out, -] Dashi (comparison test - 12 and 3) has a strong degree of adhesion.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63331835A JPH062822B2 (en) | 1988-12-29 | 1988-12-29 | Antistatic treatment method for water absorbent resin powder |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63331835A JPH062822B2 (en) | 1988-12-29 | 1988-12-29 | Antistatic treatment method for water absorbent resin powder |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02178332A true JPH02178332A (en) | 1990-07-11 |
JPH062822B2 JPH062822B2 (en) | 1994-01-12 |
Family
ID=18248179
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63331835A Expired - Fee Related JPH062822B2 (en) | 1988-12-29 | 1988-12-29 | Antistatic treatment method for water absorbent resin powder |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH062822B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5346935A (en) * | 1991-05-28 | 1994-09-13 | Takeda Chemical Industries, Ltd. | Hydrogel |
JP2004285202A (en) * | 2003-03-20 | 2004-10-14 | Nippon Shokubai Co Ltd | Water-absorbing resin composition |
JP2006075054A (en) * | 2004-09-08 | 2006-03-23 | Nippon Shokubai Co Ltd | Water-holding material for growing plant, consisting mainly of biodegradable water-absorbing resin |
JP2006075055A (en) * | 2004-09-08 | 2006-03-23 | Nippon Shokubai Co Ltd | Water-holding material for growing plant, consisting mainly of water-absorbing resin |
JP2010138278A (en) * | 2008-12-11 | 2010-06-24 | Kao Corp | Method for producing water-absorbing resin composite material |
US8765857B2 (en) * | 2003-12-05 | 2014-07-01 | Nippon Shokubai Co., Ltd. | Particulate water retaining material for cultivating plant having water absorbent resin as main component |
US8946305B2 (en) | 2011-12-22 | 2015-02-03 | Industrial Technology Research Institute | Method for crosslinking a colloid, and crosslinked colloid therefrom |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61257235A (en) * | 1985-05-08 | 1986-11-14 | Sanyo Chem Ind Ltd | Water absorbent resin composition, its preparation and water absorbent-water retention agent |
JPH0534383A (en) * | 1991-07-30 | 1993-02-09 | Seikosha Co Ltd | Camera with battery checker |
-
1988
- 1988-12-29 JP JP63331835A patent/JPH062822B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61257235A (en) * | 1985-05-08 | 1986-11-14 | Sanyo Chem Ind Ltd | Water absorbent resin composition, its preparation and water absorbent-water retention agent |
JPH0534383A (en) * | 1991-07-30 | 1993-02-09 | Seikosha Co Ltd | Camera with battery checker |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5346935A (en) * | 1991-05-28 | 1994-09-13 | Takeda Chemical Industries, Ltd. | Hydrogel |
JP2004285202A (en) * | 2003-03-20 | 2004-10-14 | Nippon Shokubai Co Ltd | Water-absorbing resin composition |
US8765857B2 (en) * | 2003-12-05 | 2014-07-01 | Nippon Shokubai Co., Ltd. | Particulate water retaining material for cultivating plant having water absorbent resin as main component |
JP2006075054A (en) * | 2004-09-08 | 2006-03-23 | Nippon Shokubai Co Ltd | Water-holding material for growing plant, consisting mainly of biodegradable water-absorbing resin |
JP2006075055A (en) * | 2004-09-08 | 2006-03-23 | Nippon Shokubai Co Ltd | Water-holding material for growing plant, consisting mainly of water-absorbing resin |
JP2010138278A (en) * | 2008-12-11 | 2010-06-24 | Kao Corp | Method for producing water-absorbing resin composite material |
US8946305B2 (en) | 2011-12-22 | 2015-02-03 | Industrial Technology Research Institute | Method for crosslinking a colloid, and crosslinked colloid therefrom |
Also Published As
Publication number | Publication date |
---|---|
JPH062822B2 (en) | 1994-01-12 |
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