JPH02104363A - Manufacture of deodorant bearer - Google Patents
Manufacture of deodorant bearerInfo
- Publication number
- JPH02104363A JPH02104363A JP63195177A JP19517788A JPH02104363A JP H02104363 A JPH02104363 A JP H02104363A JP 63195177 A JP63195177 A JP 63195177A JP 19517788 A JP19517788 A JP 19517788A JP H02104363 A JPH02104363 A JP H02104363A
- Authority
- JP
- Japan
- Prior art keywords
- film
- fine powder
- cracks
- deodorizer
- deodorizing agent
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000002781 deodorant agent Substances 0.000 title abstract description 8
- 230000001877 deodorizing effect Effects 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims description 22
- 229920000642 polymer Polymers 0.000 claims description 16
- 238000002156 mixing Methods 0.000 claims description 6
- 239000000843 powder Substances 0.000 abstract description 30
- 239000003795 chemical substances by application Substances 0.000 abstract description 12
- 239000002245 particle Substances 0.000 abstract description 3
- 230000000704 physical effect Effects 0.000 abstract description 2
- 239000010408 film Substances 0.000 description 27
- 239000004372 Polyvinyl alcohol Substances 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 6
- 235000019645 odor Nutrition 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000004408 titanium dioxide Substances 0.000 description 4
- 239000011787 zinc oxide Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003609 titanium compounds Chemical class 0.000 description 2
- QDZRBIRIPNZRSG-UHFFFAOYSA-N titanium nitrate Chemical compound [O-][N+](=O)O[Ti](O[N+]([O-])=O)(O[N+]([O-])=O)O[N+]([O-])=O QDZRBIRIPNZRSG-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 150000003752 zinc compounds Chemical class 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000010835 comparative analysis Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- DCKVFVYPWDKYDN-UHFFFAOYSA-L oxygen(2-);titanium(4+);sulfate Chemical compound [O-2].[Ti+4].[O-]S([O-])(=O)=O DCKVFVYPWDKYDN-UHFFFAOYSA-L 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910000348 titanium sulfate Inorganic materials 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、そのままでは細か過ぎて扱い難い微粉末脱臭
剤を取り扱い易くした脱臭剤担持体の製造方法に間する
ものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is directed to a method for producing a deodorizer carrier that makes it easier to handle a fine powder deodorizer that is too fine to handle as it is.
従来の技術
生活が豊かになるにつれて、奥を除去したいという要求
が、いわゆる悪臭から、日常生活におけるごく身近な奥
についてにまで及んできている。BACKGROUND OF THE INVENTION As life becomes more affluent, the demand for removing odors has expanded from so-called bad odors to even the most familiar odors in daily life.
このため、脱臭剤の開発が盛んに行われ、従来の活性炭
より逼かに優れる物質も次々と生み出されてきている。For this reason, deodorizing agents are being actively developed, and substances that are significantly superior to conventional activated carbon are being produced one after another.
その中には、本来、微粉末状や液体状で得られるものも
あるため、単に通気性袋等にパックして使うだけでなく
、紙料中に添加して紙に抄いたり、原紙に含浸させたり
、種々の形態に加工しようとする動きが活発である。Some of these substances are originally obtained in fine powder or liquid form, so they are not only used by simply packing them in breathable bags, but they can also be added to paper stock and used to make paper, or impregnated into base paper. There is an active movement toward processing the materials into various forms.
発明が解決しようとする問題点
ところで、紙料中に添加して紙に抄くにしても、その他
、m紺や発泡体等に含有させるにしても、糊成分や樹脂
自身がバインダーとして作用するため、微粉末脱臭剤は
これらバインダー成分により被膜されてしまう、これで
は、臭気成分との接触が直接的でなく、脱臭剤本来の能
力を十分に発揮できる状態にあるとは言えない。Problems to be Solved by the Invention By the way, the glue component or resin itself acts as a binder, whether it is added to the paper stock and used to make paper, or is included in navy blue, foam, etc. Therefore, the fine powder deodorizer is coated with these binder components, and in this case, the contact with the odor components is not direct, and it cannot be said that the deodorizer is in a state where it can fully demonstrate its original ability.
また、液体状の脱臭剤は勿論、微粉末状で得られるもの
でも、従来からの典型的な使い方であるところの通気性
袋等にバックして使う場合には、その粒子が細か過ぎて
、通気性袋から漏れ落ちてしまう等の問題を生ずる。か
と云って、これを樹脂に練り込んで各種形状に成形して
も、前記被膜の問題はさらに深刻となる。Furthermore, even if deodorizers are available in fine powder form as well as liquid deodorizers, the particles are too small to be used by bagging them in a breathable bag, which is the typical conventional usage. This causes problems such as leakage from the breathable bag. However, even if this is kneaded into resin and molded into various shapes, the problem with the coating becomes even more serious.
問題点を解決するための手段
したがって、上記問題点を解決するために、本第1発明
の脱臭剤担持体の製造方法は、結晶性高分子の溶液中に
微粉末脱臭剤を混合する工程と、この微粉末脱臭剤を混
合された結晶性高分子の溶液からフィルムを作る成膜工
程と、該フィルムが完全に脱水されない時点において、
過度に一軸延伸して、フィルムの分子を配向するととも
に、これによって縦方向に細断亀裂を生じさせる工程と
を有してなることを特徴とし、また、本第2発明の脱臭
剤担持体の製造方法は、結晶性高分子の溶液中に微粉末
脱臭剤を混合する工程と、この微粉末脱臭剤を混合され
た結晶性高分子の溶液からフィルムを作る成膜工程と、
該フィルムが完全に脱水されない時点において、過度に
一軸延伸して、フィルムの分子を配向するとともに、こ
れによって縦方向に亀裂を生じ易くする延伸工程と、該
延伸工程以降のフィルムに亀裂を生じさせる機械的加圧
工程とを有してなることを特徴とする。Means for Solving the Problems Therefore, in order to solve the above problems, the method for producing a deodorant carrier of the first invention includes the step of mixing a finely powdered deodorant into a solution of a crystalline polymer. , a film forming process for forming a film from a crystalline polymer solution mixed with this fine powder deodorizing agent, and a point at which the film is not completely dehydrated;
The deodorizer carrier of the second invention is characterized by comprising a step of excessively uniaxially stretching the film to orient the molecules of the film and thereby producing shredded cracks in the longitudinal direction. The manufacturing method includes a step of mixing a finely powdered deodorizing agent into a solution of a crystalline polymer, a film forming step of forming a film from a solution of a crystalline polymer mixed with this finely powdered deodorizing agent,
At a point when the film is not completely dehydrated, excessive uniaxial stretching is carried out to orient the molecules of the film, thereby making it easier to generate cracks in the longitudinal direction, and creating cracks in the film after the stretching process. It is characterized by comprising a mechanical pressurization step.
作用
結晶性高分子の溶液を成膜してフィルム状とした後、こ
れを延伸すると、分子が配向し、諸物性が改善されるこ
とは良く知られているが、延伸な一軸延伸とし、しかも
これを過度に行うと、縦方向に多数の亀裂を生じるよう
になる。It is well known that when a solution of a crystalline polymer is formed into a film and then stretched, the molecules become oriented and various physical properties are improved. If this is done excessively, a large number of cracks will occur in the longitudinal direction.
普通なら使いものにならないとされてしまうが、微粉末
脱臭剤を混合した溶液を原料としてこれを行えば、この
縦方向の多数の亀裂が発生することによって、微粉末脱
臭剤と大気との直接接触を阻害している高分子被膜が破
壊されたに等しい状態が作り出せる。したがって、−軸
延伸を過度に行って、その時点で、この亀裂を多数発生
させる、あるいは、その時点ではまだ亀裂を生じなくて
も、その後に、もむ、叩く等の外力を加えれば、容易に
亀裂が発生をするような程度にまで行えば、臭気成分と
の接触機会を十分に持った、リボン状や紐状、さらには
それらをシート状等にした脱臭剤担持体が得られる。Normally, it would be considered useless, but if this is done using a solution mixed with fine powder deodorizer as raw material, many vertical cracks will occur, which will cause direct contact between the fine powder deodorizer and the atmosphere. This creates a state that is equivalent to the destruction of the polymer coating that inhibits Therefore, - If axial stretching is performed excessively and a large number of cracks are generated at that point, or even if no cracks are generated at that point, it is easy to do so by applying external force such as kneading or tapping. If this is carried out to such an extent that cracks occur in the deodorizer, a deodorizer carrier in the form of a ribbon, string, or even a sheet can be obtained, which has sufficient opportunity for contact with odor components.
実施例
次ぎに、本発明の一実施例を説明するが、本実施例では
、微粉末脱臭剤として二酸化チタンと酸化亜鉛とを主成
分とした白色脱臭剤を、また、結晶性高分子としてポリ
ビニルアルコールを用いたものとして説明する。EXAMPLE Next, an example of the present invention will be described. In this example, a white deodorizer mainly composed of titanium dioxide and zinc oxide was used as a fine powder deodorizer, and polyvinyl was used as a crystalline polymer. This will be explained assuming that alcohol is used.
ここで、二酸化チタンと酸化亜鉛とを主成分とした微粉
末脱臭剤は、特開昭63−54935号公報に詳述され
ており、このものは、二酸化チタンと酸化亜鉛とを主体
とし、幾分の水成分を含んでなり、脱臭力を比較評価す
る目安としてのアンモニア、硫化水素の低温、低濃度吸
着性に特に優れる白色の微粉末状のものであり、触媒作
用によって悪臭分子を低分子化することによって脱臭を
図るとともに、さらに、酸化亜鉛は酸性ガスを化学吸着
し、二酸化チタンはアルカリ性ガスを物理吸着すると考
えられるものである。また、これは、水に可溶なチタン
化合物と水に可溶な亜鉛化合物との水溶液と、アルカリ
水溶液とを混合し、生成する沈澱物を乾燥して得られる
もので、例えば、硫酸チタン、塩化チタン、硝酸チタン
、硫酸亜鉛、塩化亜鉛、硝酸亜鉛等、チタン化合物と亜
鉛化合物とをモル比で7:3〜3ニアの範囲とした混成
水溶液に、水酸化ナトリウム、水酸化カリウム、水酸化
バリウム、アンモニア等のアルカリ水溶液を一部づつ又
は全部を、40〜60℃の反応温度にて、M終的にPH
7〜9の範囲で混合し、生成する沈澱物を150〜22
0℃で乾燥したものが好適とされているものである。そ
して、このような微粉末脱臭剤にチタン工業株式会社が
製造販売するものがある、(以下、これをTZ脱臭剤と
称す。)
そこで、先ず、このTZ脱臭剤とポリビニルアルコール
とを混合した水溶液を作るが、これには図示を略すが、
粉末または粒状のポリビニルアルコールを溶解槽に投入
するとともに水を加えて攪はん混合し、以て糊状の高い
粘度のポリビニルアルコール水溶液、いわゆるドープを
作り、これと同時にまたは前後してTZ脱臭剤を上記溶
解槽に加えて微粉末脱臭剤入りのドープを作ればよい。Here, a fine powder deodorizer mainly composed of titanium dioxide and zinc oxide is described in detail in JP-A No. 63-54935. It is a fine white powder that is particularly good at adsorbing ammonia and hydrogen sulfide at low temperatures and at low concentrations, which is used as a guideline for comparative evaluation of deodorizing power. It is thought that zinc oxide chemically adsorbs acidic gases, and titanium dioxide physically adsorbs alkaline gases. Also, it is obtained by mixing an aqueous solution of a water-soluble titanium compound and a water-soluble zinc compound with an alkaline aqueous solution and drying the resulting precipitate.For example, titanium sulfate, Add sodium hydroxide, potassium hydroxide, and hydroxide to a mixed aqueous solution containing a titanium compound and a zinc compound such as titanium chloride, titanium nitrate, zinc sulfate, zinc chloride, and zinc nitrate in a molar ratio of 7:3 to 3. Aqueous alkaline solutions such as barium, ammonia, etc. are added in part or in whole at a reaction temperature of 40 to 60°C until the final PH
Mix in the range of 7 to 9, and the resulting precipitate to 150 to 22
It is preferable to dry it at 0°C. There is a fine powder deodorizer like this manufactured and sold by Titan Industries Co., Ltd. (hereinafter referred to as TZ deodorizer).Therefore, first, an aqueous solution of this TZ deodorizer and polyvinyl alcohol was prepared. Although not shown in the diagram,
Powdered or granular polyvinyl alcohol is put into a dissolution tank and water is added and mixed by stirring to make a paste-like, highly viscous polyvinyl alcohol aqueous solution, so-called dope, and at the same time or before or after this, TZ deodorizer is added. can be added to the above-mentioned dissolving tank to make a dope containing a finely powdered deodorizing agent.
このようにして微粉末脱臭剤入りのドープAが得られた
ら、ろ過、脱泡した後、第1図に示すごとく、これをホ
ッパー1に導くとともに、このホッパー1の底の間口か
ら、これに近接して設けられて、ゆっくり回転している
大径の金属ドラム2上に均−薄膜状に流延する。そして
、この金属ドラム2の周囲には覆い3が設けられており
、ここには熱風が導入されていて、金属ドラム2上のド
ープは水分蒸発されて、ゲル状のフィルムBとなり、一
端より剥離されて覆い3外へ取り出される。When dope A containing a fine powder deodorizer is obtained in this way, it is filtered and defoamed, and then introduced into the hopper 1 as shown in Figure 1. A thin film is uniformly cast onto a large-diameter metal drum 2 which is placed close to each other and rotates slowly. A cover 3 is provided around the metal drum 2, into which hot air is introduced, and the dope on the metal drum 2 is evaporated to become a gel-like film B, which is peeled off from one end. is removed from the cover 3.
その後、水分蒸発程度が十分でなければ、乾燥室4へ送
られ、ここで乾燥促進されて、未だゲル化状態のままで
次ぎの延伸工程へ送られる。Thereafter, if the degree of water evaporation is not sufficient, it is sent to the drying chamber 4, where it is accelerated in drying and sent to the next stretching process while still in a gelled state.
延伸工程では、−軸延伸であって、しかも、これを過度
に行う必要がある。In the stretching process, it is necessary to carry out -axis stretching, and to perform this in an excessive manner.
本実施例では、同図に示すごとく、延伸方向に遅駆動ロ
ール6と早駆動ロール6とを前後に配し、その駆動速度
の差によって、延伸するようにしている。なお、これら
駆動ロール6.6は、フィルムのゲル化状態により適宜
加熱、場合によっては冷却を施すのが望まれる。而して
、この遅駆動ロール6と早駆動ロール6との駆動速度の
差は、従来適当とされていた値よりも相当程度大きな値
として、フィルム分子の配向を過度に行わせることによ
って、縦方向の亀裂を生ずる、あるいは、その後、もむ
、叩く等の機械的圧力を加えれば、それだけで、縦方向
に亀裂を生ずる程度にまで行う。In this embodiment, as shown in the figure, a slow-driving roll 6 and a fast-driving roll 6 are arranged in front and behind each other in the stretching direction, and stretching is performed by the difference in driving speed. Note that it is desirable that these drive rolls 6.6 be appropriately heated and, in some cases, cooled, depending on the gelling state of the film. The difference in driving speed between the slow-driving roll 6 and the fast-driving roll 6 is set to a value considerably larger than the value conventionally considered appropriate, and by excessively orienting the film molecules, the vertical If mechanical pressure such as kneading or pounding is applied after that, it can be sufficient to cause cracks in the longitudinal direction.
したがって、この延伸工程を経た後には、フィルムに縦
方向の亀裂が多数入っているか、その時 2には入って
いなくとも、これに機械的外力を加えれば、さっと亀裂
が入る状態となっている。Therefore, after this stretching process, the film will have many longitudinal cracks, or even if there are no cracks at that time, if an external mechanical force is applied to it, the film will easily crack.
本実施例では、この機械的加圧工程として、螺旋状に凹
凸を形成した一対のゴムロール7を前後に二組み設け、
上記延伸工程を経たフィルムをこのゴムロール7間を通
過させることによって、縦方向の亀裂を確実に生じさせ
るようにしている。In this embodiment, for this mechanical pressurizing process, two sets of a pair of rubber rolls 7 having spirally uneven surfaces are provided at the front and rear.
By passing the film that has undergone the above-mentioned stretching process between the rubber rolls 7, cracks in the longitudinal direction are reliably generated.
そして、本実施例では、その後、熱固定させるために乾
燥室8を通過させ、その先方にギロチンカッター9を配
置して適当長さ毎にカットして短冊状の細片Cとして取
り出せるようになっている。In this embodiment, the material is then passed through a drying chamber 8 for heat-setting, and a guillotine cutter 9 is placed in front of the drying chamber 8 so that it can be cut into appropriate lengths and taken out as strip-shaped strips C. ing.
なお、前記原料としてのポリビニルアルコールは、完全
けん化したものを用いてもよいし、また、部分けん化し
たものを用いてもよい。完全けん化したものを用いたと
きは、水に不溶の担持体が得られ、部分けん化したもの
を用いたとき水に可溶の担持体が得られる。このため、
例えば、両者側々に短冊状の細片に仕上げた後、両者を
混合し、これをシート状に配置して、霧氷を振りかけ、
乾燥させれば、不織布様の担持体を得ることもできる。The polyvinyl alcohol used as the raw material may be completely saponified or partially saponified. When a completely saponified product is used, a water-insoluble carrier is obtained, and when a partially saponified product is used, a water-soluble carrier is obtained. For this reason,
For example, after cutting both sides into strips, mixing the two, arranging this into a sheet, and sprinkling with hoarfrost,
By drying, a nonwoven fabric-like carrier can be obtained.
また、原料ポリビニルアルコールには、グリセリンやグ
リコール類を可塑剤として加え、また、TZ脱臭剤の分
散性が劣るようであればいわゆるカップリング剤等で処
理して混合させるようにしてもよいこと勿論である。In addition, glycerin or glycols may be added as a plasticizer to the raw material polyvinyl alcohol, and if the dispersibility of the TZ deodorizer is poor, it is of course possible to treat it with a so-called coupling agent and mix it. It is.
以上の工程において、どのような結晶性高分子を原料と
するにせよ、その溶液中に微粉末脱臭剤が混合された後
、フィルムに成形されるため、微粉末脱臭剤は原料高分
子により被膜された状態として仕上げられるのが普通で
ある。実施例でも、フィルムに成膜された当初は、TZ
脱臭剤の各微粉末の回りを極めて薄い層ではあるが、ポ
リビニルアルコールが被膜する状態となっている。In the above process, no matter what kind of crystalline polymer is used as the raw material, the fine powder deodorizer is mixed into the solution and then formed into a film, so the fine powder deodorizer is coated with the raw material polymer. It is usually finished in a polished state. In the examples as well, when the film was initially formed, TZ
Each fine powder of the deodorizing agent is surrounded by a very thin layer of polyvinyl alcohol.
ところが、本発明では、フィルムはゲル状態で延伸され
るため、微粉末脱臭剤上の被膜が薄化されて有利となる
のは勿論、この延伸が一軸延伸であって、従来通常のフ
ィルムを作るとき適当とされていた程度よりも相当過度
であって、縦方向に亀裂が容易に入る程度、さらには、
その時既に縦方向に亀裂が生ずる程度にまで行われるた
め、微粉末脱臭剤上の被膜が破られたに等しい破断面が
自然と形成されることとなっている。一方、微粉末脱臭
剤は、この破断面が微粉末脱臭剤の位置する真中央で発
生することは極めて希であるから、左右何れか側に固定
、担持されていることに変わりない。However, in the present invention, since the film is stretched in a gel state, the film on the fine powder deodorizer is thinned, which is advantageous. It is considerably excessive than what was considered appropriate at the time, and the cracks easily form in the longitudinal direction, and furthermore,
At that time, the process is carried out to such an extent that cracks are already formed in the longitudinal direction, so a fractured surface is naturally formed, which is equivalent to breaking the coating on the fine powder deodorizer. On the other hand, in the case of a fine powder deodorizing agent, it is extremely rare for this fracture surface to occur at the exact center where the fine powder deodorizing agent is located, so it remains fixed and supported on either the left or right side.
また、本実施例では、その後、さらに、これを短尺にギ
ロチンカッターで切断しているため、微粉末脱臭剤を覆
っている被膜はその部分においても破られる可能性があ
り、また、短冊状とされることにより、取り扱い易くな
っている。In addition, in this example, since this is further cut into short pieces with a guillotine cutter, the film covering the fine powder deodorizer may be torn at that part as well, and the film may not be cut into strips. This makes it easier to handle.
したがって、−旦高分子により被膜された微粉末脱臭剤
の相当数が、その被膜を破られたに等しい状態とされる
から、臭気成分との直接接触の機会を多く持って、微粉
末脱臭剤が本来の性能を発揮し得るようになり、同時に
、全体としては適度な大きさとして仕上げられているか
ら、取り扱い易くもなっている。このため、これを通気
性袋に入れて使ったり、シート状に仕上げてフィルター
にする等様々な形での使用が可能となっている。Therefore, since a considerable number of fine powder deodorizers coated with polymers are in a state equivalent to having their coating broken, the fine powder deodorizer has many opportunities to come into direct contact with odor components. It is now able to demonstrate its original performance, and at the same time, the overall size is appropriate, making it easy to handle. Therefore, it can be used in a variety of ways, such as by putting it in a breathable bag or making it into a sheet to make a filter.
また、上記実施例のような白色系の脱臭剤を用いれば、
出来上がる担持体も白色系の清潔感あるものとなり、ま
た、自由な着色も可能であるため、従来の脱臭剤のイメ
ージを一新した使い方もできるようになる。In addition, if a white deodorizer like the one in the above example is used,
The resulting carrier also has a clean, white color, and can be colored as desired, making it possible to use it in a completely new way than conventional deodorants.
以上、微粉末脱臭剤として、二酸化チタンと酸化亜鉛と
を主成分とするTZ脱臭剤を例に説明したが、本発明に
用いる微粉末脱臭剤はこのTZ脱臭剤に限らず、他の微
粉末脱臭剤であっても同様に施用できるのは勿論であり
、また、結晶性高分子も実施例のポリビニルアルコール
に限られるものでなく、延伸して配向する高分子であれ
ば利用できる。また、上記実施例では、成膜するのに、
いわゆるキャスティング法、そのうちでもドラム式によ
るものとして説明したが、これに限るものでなく、各種
の成膜法が利用でき、また、延伸法についても同様に上
記実施例に限るものでなく、各種の延伸法が利用できる
。また、上記実施例では、延伸工程後に、機械的圧力を
加えるゴムロール、さらにはギロチンカッターを配し、
亀裂発生を促進した後、短冊状にカットするようにした
が、これに限らず、延伸工程で十分な亀裂が生じていれ
ば、それだけで、仕上がった脱臭剤担持体としてもよい
。このようにして得られた担持体は、例えば、これを折
り重ねて、フィルターとして使ったりすることができる
。Above, the fine powder deodorizer has been explained using the TZ deodorizer whose main components are titanium dioxide and zinc oxide as an example, but the fine powder deodorizer used in the present invention is not limited to this TZ deodorizer. Of course, a deodorizing agent can also be applied in the same way, and the crystalline polymer is not limited to the polyvinyl alcohol in the example, but any polymer that can be stretched and oriented can be used. In addition, in the above embodiment, in order to form a film,
Although the so-called casting method, in particular a drum method, has been described, the method is not limited to this, and various film forming methods can be used. Similarly, the stretching method is not limited to the above embodiments, and various film forming methods can be used. Stretching methods are available. In addition, in the above embodiment, after the stretching process, a rubber roll that applies mechanical pressure and a guillotine cutter are arranged.
After promoting the generation of cracks, the strips are cut into strips; however, the present invention is not limited to this, and as long as sufficient cracks are generated during the stretching process, it may be used as a finished deodorizer carrier. The carrier thus obtained can be used as a filter by folding it, for example.
発明の効果
したがって、本発明によれば、微粉末脱臭剤上の高分子
被膜が破られたに等しい状態に仕上げられるので、脱臭
剤本来の脱臭力を発揮することができる担持体が得られ
る。また、微粉末脱臭剤が脱落してくる可能性は少なく
、非常に取り扱い易く、種々の形態で利用できるものが
得られる。Effects of the Invention Therefore, according to the present invention, the polymer film on the fine powder deodorizer is finished in a state equivalent to being broken, so a carrier can be obtained that can exert the deodorizing power inherent to the deodorant. Furthermore, there is little possibility that the fine powder deodorizer will fall off, making it extremely easy to handle and usable in various forms.
第1図は本発明方法の一実施例の工程を示す略解図であ
る。
A・・・微粉末脱臭剤入りポリビニルアルコール溶液B
・・・ゲル状態のフィルム
C・・・短冊状とされた脱臭剤担持体
特許出願人 株式会社キュービック
エンジニアリング 代表者中西幹育FIG. 1 is a schematic diagram showing the steps of an embodiment of the method of the present invention. A: Polyvinyl alcohol solution B containing fine powder deodorizer
... Film C in gel state ... Deodorizer carrier in the form of strips Patent applicant: Cubic Engineering Co., Ltd. Representative: Mikiku Nakanishi
Claims (2)
工程と、この微粉末脱臭剤を混合された結晶性高分子の
溶液からフィルムを作る成膜工程と、該フィルムが完全
に脱水されない時点において、過度に一軸延伸して、フ
ィルムの分子を配向するとともに、これによって縦方向
に亀裂を生じさせる工程とを有してなることを特徴とす
る脱臭剤担持体の製造方法。(1) A step of mixing a finely powdered deodorizing agent into a solution of a crystalline polymer, a film forming step of forming a film from a solution of a crystalline polymer mixed with this finely powdered deodorizing agent, and a step of forming a film completely. 1. A method for producing a deodorizer carrier, which comprises the step of excessively uniaxially stretching the film at a time when the film is not dehydrated to orient the molecules of the film and thereby generate cracks in the longitudinal direction.
工程と、この微粉末脱臭剤を混合された結晶性高分子の
溶液からフィルムを作る成膜工程と、該フィルムが完全
に脱水されない時点において、過度に一軸延伸して、フ
ィルムの分子を配向するとともに、これによって縦方向
に亀裂を生じ易くする延伸工程と、該延伸工程以降のフ
ィルムに亀裂を生じさせる機械的加圧工程とを有してな
ることを特徴とする脱臭剤担持体の製造方法。(2) A step of mixing a finely powdered deodorizing agent into a solution of a crystalline polymer, a film forming step of forming a film from a solution of a crystalline polymer mixed with this finely powdered deodorizing agent, and a step of forming a film completely. A stretching process in which the film is uniaxially stretched excessively at a time when it is not dehydrated to orient the molecules of the film and thereby make it easier to cause cracks in the longitudinal direction; and a mechanical pressure process to cause cracks in the film after the stretching process. A method for producing a deodorizer carrier, comprising:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63195177A JP2794419B2 (en) | 1988-08-04 | 1988-08-04 | Method for producing deodorant carrier |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63195177A JP2794419B2 (en) | 1988-08-04 | 1988-08-04 | Method for producing deodorant carrier |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02104363A true JPH02104363A (en) | 1990-04-17 |
| JP2794419B2 JP2794419B2 (en) | 1998-09-03 |
Family
ID=16336728
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63195177A Expired - Fee Related JP2794419B2 (en) | 1988-08-04 | 1988-08-04 | Method for producing deodorant carrier |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2794419B2 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6448140U (en) * | 1987-09-21 | 1989-03-24 |
-
1988
- 1988-08-04 JP JP63195177A patent/JP2794419B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6448140U (en) * | 1987-09-21 | 1989-03-24 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2794419B2 (en) | 1998-09-03 |
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