JPH0642902B2 - Gel type deodorant - Google Patents
Gel type deodorantInfo
- Publication number
- JPH0642902B2 JPH0642902B2 JP63223627A JP22362788A JPH0642902B2 JP H0642902 B2 JPH0642902 B2 JP H0642902B2 JP 63223627 A JP63223627 A JP 63223627A JP 22362788 A JP22362788 A JP 22362788A JP H0642902 B2 JPH0642902 B2 JP H0642902B2
- Authority
- JP
- Japan
- Prior art keywords
- gel
- deodorant
- odor
- type
- type deodorant
- 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 - Fee Related
Links
- 239000002781 deodorant agent Substances 0.000 title claims description 41
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 18
- -1 betaine compound Chemical class 0.000 claims description 10
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 claims description 9
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 claims description 8
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 6
- 238000006757 chemical reactions by type Methods 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 229920000058 polyacrylate Polymers 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 2
- 229960003237 betaine Drugs 0.000 claims description 2
- 239000000499 gel Substances 0.000 description 39
- 235000019645 odor Nutrition 0.000 description 23
- 230000001877 deodorizing effect Effects 0.000 description 13
- 238000004332 deodorization Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 6
- 238000001879 gelation Methods 0.000 description 6
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229930014626 natural product Natural products 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 235000019615 sensations Nutrition 0.000 description 2
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- CUGZWHZWSVUSBE-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxy)ethanol Chemical compound OCCOCC1CO1 CUGZWHZWSVUSBE-UHFFFAOYSA-N 0.000 description 1
- HDPLHDGYGLENEI-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COC(C)COCC1CO1 HDPLHDGYGLENEI-UHFFFAOYSA-N 0.000 description 1
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 description 1
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241001312219 Amorphophallus konjac Species 0.000 description 1
- 235000001206 Amorphophallus rivieri Nutrition 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920002752 Konjac Polymers 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical class C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 235000013527 bean curd Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000000252 konjac Substances 0.000 description 1
- 235000010485 konjac Nutrition 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004899 motility Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 230000008786 sensory perception of smell Effects 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229940032147 starch Drugs 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明はゲル化剤を用いて脱臭剤をゲル化し、これを臭
気発生場所(例えば、冷蔵庫内、トイレ内、室内、車内
など)に設置するだけで悪臭を除去できる脱臭剤に関す
る。DETAILED DESCRIPTION OF THE INVENTION (Industrial field of application) The present invention uses a gelling agent to gel a deodorant and installs it in an odor generating place (for example, in a refrigerator, a toilet, a room, a car, etc.). The present invention relates to a deodorant capable of removing a bad odor just by performing.
(従来の技術及び発明が解決しようとする課題) 脱臭剤に関する特許発明は非常に多く、それらは次の4
種類の方法に分類できる。(Prior Art and Problems to be Solved by the Invention) There are a large number of patented inventions relating to deodorants.
It can be classified into various methods.
(1)感覚によるもの(嗅覚に作用する) (2)物理的な吸着によるもの (3)微生物によるもの (4)化学反応によるもの これらについて、(1)は香料を用いるいわゆるマスキン
グ法であるが、悪臭と混合されかえつて不快に感ずる場
合がある。(2)は活性炭が主流であるが水分に対して弱
いほかに、人間にとつて好ましい臭気も吸着してしま
う。(3)は速効性が弱く管法も困難である場合が多い。
以上に対して(4)は瞬間的に効果があらわれ、使用する
薬剤を適切に選択することによつて取り扱いも極めて容
易かつ安全で、目的とする脱臭を確実に行える方法であ
る。(1) Sensation (acts on olfaction) (2) Physical adsorption (3) Microorganism (4) Chemical reaction For these, (1) is a so-called masking method using a fragrance, , It may be mixed with a foul odor and feel uncomfortable. In (2), activated carbon is the mainstream, but it is weak against moisture, and it also absorbs odors that are preferable to humans. In (3), the fast-acting effect is weak and the tube method is often difficult.
On the other hand, (4) is a method that is effective instantaneously, is extremely easy and safe to handle by properly selecting the drug to be used, and can surely achieve the target deodorization.
本発明は、この化学反応型の脱臭剤をゲル内に含有させ
たゲル型脱臭剤を提供するものである。現在、臭気発生
場所として問題になる所は冷蔵庫内、トイレ内(家庭、
バス、車両、飛行機等)、自動車内などでありいずれの
場合も密閉空間になり易く、臭気の拡散効率が極めて不
良な場所といえる。このような空間部に薬剤などを噴霧
することはできるだけ避けることが望ましく、その解決
策として最も一般的に使用されるのが活性炭、もしくは
芳香剤などである。両者で脱臭能力を有するものは勿論
活性炭であが、活性炭は水分で劣化するほか悪臭以外に
も、例えば芳香剤からの香りや悪臭とは感じない臭気を
も吸着してしまい、実際の悪臭が生じた場合には能力が
軽減している場合が多々ある。これに対して、化学反応
型ゲル型脱臭剤は含有させる薬剤により、選うい択的に
悪臭のみと反応し、しかも日数の経過とともにゲル内に
含まれる水分が蒸発し、ゲルが縮少していくため交換時
期を目視で判断できる利点を有するのである。また、臭
気発生場所に液体状脱臭剤を容器に入れておく方法も可
能であるが、振動及び倒れたりした場合、液体は容易に
流れ出し周辺を汚染する欠点をもつ。しかし、液体状脱
臭剤をゲル化すればこのような問題は一挙に解決できる
のである。また、現在市販されているゲル型脱臭剤もあ
るが満足できる脱臭能力を持たない(比較品として実施
例3に記載)。The present invention provides a gel type deodorant containing the chemical reaction type deodorant in a gel. Currently, odors are generated in the refrigerator and toilets (home,
It can be said that it is a place where a closed space is easily formed in any case such as a bus, a vehicle, an airplane, etc.) and an automobile, and the odor diffusion efficiency is extremely poor. It is desirable to avoid spraying a drug or the like into such a space as much as possible, and the most commonly used solution is activated carbon or a fragrance. Both of them have deodorizing ability, of course, activated carbon, but activated carbon deteriorates due to moisture, and in addition to bad odors, it also absorbs scents from fragrances and odors that do not feel bad, and the actual bad odors When they do occur, their abilities are often diminished. On the other hand, the chemical reaction type gel deodorant selectively reacts with only the bad odor depending on the contained agent, and the water contained in the gel evaporates with the passage of days, and the gel shrinks. Therefore, there is an advantage that the replacement time can be visually judged. Further, a method of putting a liquid deodorant in a container at the place where the odor is generated is also possible, but when vibrated or collapsed, the liquid easily flows out and contaminates the surrounding area. However, such problems can be solved all at once by gelling the liquid deodorant. Further, there are gel type deodorizing agents which are currently on the market, but they do not have a satisfactory deodorizing ability (described in Example 3 as a comparative product).
(課題を解決するための手段) 本発明は前記の課題を解決するためになされたものであ
り、新規なゲル型脱臭剤を提供するものである。すなわ
ち、本発明のゲル型脱臭剤は分子量が40,000から300,00
0までのポリアクリル酸ナトリウム又はポリアクリル酸
アンモニウムの2乃至30重量%と、ジグリシジルエー
テル又はポリグリシジルエーテルの1乃至10重量%
と、ベタイン型化合物を有効成分とする化学反応型脱臭
剤の5乃至40重量%とを含有し、残部が水より成るこ
とを特徴とするものである。(Means for Solving the Problems) The present invention has been made to solve the above problems, and provides a novel gel-type deodorant. That is, the gel type deodorant of the present invention has a molecular weight of 40,000 to 300,00.
2 to 30% by weight of sodium polyacrylate or ammonium polyacrylate up to 0 and 1 to 10% by weight of diglycidyl ether or polyglycidyl ether
And 5 to 40% by weight of a chemically reactive deodorant containing a betaine compound as an active ingredient, and the balance being water.
ここにいうゲルとは化学大辞典(共立出版(株)1981年
版)によると「コロイド粒子又は高分子溶質が相互作用
のために独立した運動性を失つて集合した構造を持ち固
化した状態をいう。」と記載されている。我々の日常身
の回りにも豆腐、こんにやく、かまぼこ、プリン、ゼ
ー、卵などの食品類、紙オムツ、生理用品、芳香剤など
の生活用品にゲル物質が数多く認められる。ゲル形成性
物質は通常、天然物と合成物とに分類され代表的な物質
は次のとおりである。According to the Chemical Dictionary (Kyoritsu Shuppan Co., Ltd., 1981 edition), the gel here refers to "a state in which colloidal particles or polymer solutes lose their independent motility due to an interaction and have an assembled structure and are solidified. . "Is described. Many gel substances are found in our daily lives such as tofu, konjac, kamaboko, pudding, zee, eggs, and other foods, disposable diapers, sanitary products, and fragrances. Gel-forming substances are usually classified into natural products and synthetic products, and representative substances are as follows.
天然物…寒天,ゼラチン,卵白,デンプン, カラゲナン,アルギン酸ナトリウム等 合成物…ポリビニルアルコール,カルボキシメ チルセルロース,ポリアアクリル酸ナト リウム,ポリアクリロアミド等 ゲル化機構としては、天然物の場合高分子の分子間力に
依存している場合が一般的で、加熱・冷却によりゲルと
ゾルとの間で可逆的な挙動を示す。これに対して合成物
では光や放射線による架橋反応で三次元網状化する場合
と、架橋剤によつて三次元網状化する場合とがある。こ
のときの架橋点の結合部は共有結合であるため、天然物
のように温度変化によるゲルとゾル間の可逆性は非常に
乏しくなり、むしろ不可逆性といえる。我々はゲル型脱
臭剤の使用用途として前述した冷蔵庫内、トイレ内、自
動車内などを考えておりこれらの場合の使用温度は、夏
季の駐車中の自動車内では50〜70℃、冷蔵庫内では
0〜4℃とかなり幅広い苛酷な温度条件下になるのであ
る。従つて、天然物などのように加熱・冷却によつてゲ
ル−ゾル間の可逆性をもつことは好ましくない。このよ
うな理由から我々は温度変化でのゲル−ゾル間の可逆性
のない合成物のゲル形成性物質と架橋剤を選択し、さら
に得られたゲル内への脱臭剤の配合を試みた。使用した
ポリアクリル酸ナトリウム、又はポリアクリル酸アンモ
ニウムの分子量は市販品の10,000,40,000,140,000,2
80,000の4種類である。しかしながら実施例で後述する
ように分子量10,000については好適でないことが判明し
たので本発明からは除外することとした。又、その配合
量を全組成の2乃至30重量%としたのは好適なゲルを
得るための好ましい範囲であるからである。Natural products: agar, gelatin, egg white, starch, carrageenan, sodium alginate, etc. Synthetic products: polyvinyl alcohol, carboxymethyl cellulose, sodium polyacrylate, polyacryloamide, etc. It is generally dependent on intermolecular force, and exhibits reversible behavior between gel and sol by heating / cooling. On the other hand, the compound may be three-dimensionally reticulated by a crosslinking reaction by light or radiation, or may be three-dimensionally reticulated by a crosslinking agent. At this time, since the bonding portion at the cross-linking point is a covalent bond, the reversibility between the gel and the sol due to temperature change becomes very poor as in a natural product, and it can be said that it is irreversible. We are considering the use of the gel type deodorant in the above-mentioned refrigerator, toilet, automobile, etc. The operating temperature in these cases is 50 to 70 ° C in the automobile parked in summer and 0 in the refrigerator. It is under a wide range of severe temperature conditions of ~ 4 ° C. Therefore, it is not preferable to have reversibility between the gel and the sol by heating and cooling such as natural products. For these reasons, we have selected a gel-forming substance and a cross-linking agent which are not reversible between gel and sol due to temperature change, and have tried to incorporate a deodorant into the resulting gel. The molecular weight of sodium polyacrylate or ammonium polyacrylate used was 10,000, 40,000, 140,000, 2
There are four types of 80,000. However, as will be described later in the examples, it was found that a molecular weight of 10,000 was not suitable, so it was decided to exclude it from the present invention. Further, the amount thereof is set to 2 to 30% by weight of the total composition because it is a preferable range for obtaining a suitable gel.
架橋剤としては通常アルデヒド化合物、アミン化合物、
オキシラン化合物などが使用されるが本発明ではオキシ
ラン化合物を選択した。他のアルデヒド化合物及びアミ
ン化合物は一般的にそれ自身のもつ臭気が強く不適と判
断したからである。さらに、オキシラン化合物として市
販品のジグリシジルエーテル又はポリグリシジルエーテ
ルを選んだ。ジグリシジルエーテルとしてはエチレング
リコールグリシジルエーテル,ポリエチレングリコール
ジグリシジルエーテル,プロピレングリコールジグリシ
ジルエーテル,ポリプロピレングリコールジグリシジル
エーテル ネオペンチルグリコールジグリシジルエーテ
ル、又、ポリグリシジルエーテルとしてはトリメチロー
ルプロパンポリグリシジルエーテル,ポリグセロールポ
リグリシジルエーテル,グリセロールポリグリシジルエ
ーテル,ジグリセロールポリグリシジルエーテルがあげ
られる。その配合量を全組成の1乃至10重量%とした
のは、これも好適なゲルを得るための好ましい範囲であ
ることによる。As the crosslinking agent, usually an aldehyde compound, an amine compound,
Although an oxirane compound or the like is used, the oxirane compound is selected in the present invention. This is because other aldehyde compounds and amine compounds generally have strong odors and are judged to be unsuitable. Furthermore, commercially available diglycidyl ether or polyglycidyl ether was selected as the oxirane compound. Examples of diglycidyl ethers include ethylene glycol glycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, neopentyl glycol diglycidyl ether, and polyglycidyl ethers such as trimethylolpropane polyglycidyl ether and polyglyceride. Examples include roll polyglycidyl ether, glycerol polyglycidyl ether, and diglycerol polyglycidyl ether. The blending amount is set to 1 to 10% by weight of the total composition because this is also a preferable range for obtaining a suitable gel.
ベタイン型化合物を有効成分とする化学反応型脱臭剤と
しては市販されている薬剤「自社品商品名:エポリオン
(登録商標)」を使用した。その全組成に対する配合量
は5乃至40重量%の範囲としたがこの範囲内において
ゲル強度(ゲルとして形態を保つか否か)との相関で、
任意に選択できる。この脱臭剤は本発明者の発明に係り
特開昭62−102760号公報(特願昭62−242922号)に開示
されたものの実施商品である。本発明におけるこの脱臭
剤の選択理由は、それが化学反応型脱臭剤の中で特にア
ンモニア又はトリメチルアミンの如きアルカリ臭並びに
硫化水素又はメチルメルカプタンの如き酸性臭に対して
脱臭能にすぐれるほか無色透明液体であり、ゲルに含有
させた場合に着色しないこと、さらに無臭であることで
ある。ちなみに、市場に出廻つている天然抽出物と称さ
れる脱臭剤には、独特の臭気を有しているものが多い。As the chemical reaction type deodorant containing a betaine type compound as an active ingredient, a commercially available drug “In-house product, trade name: Epolion (registered trademark)” was used. The compounding amount with respect to the total composition was set in the range of 5 to 40% by weight, but in this range, the correlation with the gel strength (whether or not to maintain the form as a gel),
It can be arbitrarily selected. This deodorant is a commercial product of the one disclosed in Japanese Patent Application Laid-Open No. 62-102760 (Japanese Patent Application No. 62-242922) relating to the invention of the present inventor. The reason for selecting this deodorant in the present invention is that it is excellent in deodorizing ability especially against alkaline odors such as ammonia or trimethylamine and acidic odors such as hydrogen sulfide or methyl mercaptan among the chemical reaction type deodorants and it is colorless and transparent. It is a liquid, does not color when contained in a gel, and is odorless. By the way, many of the deodorants called natural extracts on the market have a unique odor.
(作用) 表−1に自社商品エポリオンER−10型、エポリオンN−
100型、及びエポリオンS型の三種についての脱臭試験
結果と、比較のために市販されている溶液型脱臭剤、A
〜D社の四種についての脱臭能力を記載した。(Action) Table-1 shows our own products, Epolion ER-10 type, Epolion N-
Deodorant test results for 100 type and Epolion S type, and a solution type deodorant commercially available for comparison, A
~ The deodorizing ability for four types of Company D is described.
試験方法:500ml三角フラスコを使つてのヘツ ドスペース法。 Test method: Headspace method using a 500 ml Erlenmeyer flask.
(1)脱臭剤の使用量=1.0ml (2)水の使用量=10.0ml(振とう中脱臭剤がフラスコ内
で均一にかき混ぜられるようにするため使用した。) (3) 温 度=室温(25℃) (4) 振とう時間=5分間 (5) 臭気ガス濃度=表−1中にブランク値として記
載。(予じめ調製したそれぞれの臭気溶液1.0mlをフラ
スコ内に計り取つた。) (6) 測定法=北川式ガス検知管使用 尚、各々の液量の測定にはホールピペツトを使用した。
表−1より明らかなように外観、臭気、pH、及び脱臭能
力などを総合的に考慮すると、エポリオンN−100型
がゲルへの含有脱臭剤として適当であると判断される。
また、各種臭気物質への反応機構は次のとおりである
(特開昭62−102760号公報)。(1) Amount of deodorant used = 1.0 ml (2) Amount of water used = 10.0 ml (Used so that the deodorant can be uniformly mixed in the flask during shaking.) (3) Temperature = room temperature (25 ° C) (4) Shaking time = 5 minutes (5) Odor gas concentration = described as a blank value in Table-1. (1.0 ml of each preliminarily prepared odor solution was weighed into a flask.) (6) Measurement method = Kitagawa type gas detector tube A hole pipette was used to measure each liquid amount.
As is clear from Table 1, when comprehensively considering the appearance, odor, pH, deodorizing ability, etc., it is judged that Epolion N-100 type is suitable as the deodorant contained in the gel.
Further, the reaction mechanism for various odorous substances is as follows (JP-A-62-102760).
(1) -COOH+NH3→-COONH4 (2) -COOH+N(CH3)3→-COONH(CH3)3 (3) (4) 従つて、ゲルに脱臭剤を含有させた場合、上式と同様の
反応がゲル表面にて生起し、脱臭反応が進行する。(1) -COOH + NH 3 → -COONH 4 (2) -COOH + N (CH 3 ) 3 → -COONH (CH 3 ) 3 (3) (Four) Therefore, when the gel contains a deodorant, a reaction similar to the above formula occurs on the gel surface, and the deodorization reaction proceeds.
(実施例) 本発明の内容をさらに実施例にもとづいて詳細に説明す
る。(Example) The content of the present invention will be described in more detail based on examples.
実施例1(ゲルの形成) 分子量の異なる4種のポリアクリル酸ナトリウムと、グ
リシジルエーテルとしてポリエチレングリコールジグリ
シジルエーテルを使用した場のゲル化状態を表2に示
す。なお、表中試料NO.a,bは比較例とした。Example 1 (Formation of gel) Table 2 shows the gelation state when four types of sodium polyacrylate having different molecular weights and polyethylene glycol diglycidyl ether were used as the glycidyl ether. In addition, sample Nos. A and b in the table are comparative examples.
また、表2においてゲル化条件は55℃×24hrとし
た。 Further, in Table 2, the gelling condition was 55 ° C. × 24 hr.
前述したようにゲル型脱臭剤の大きなメリツトは、目視
によつて交換時期が判断できることである。即ち、理想
的には最終段階で残留物が全くなくなることが望ましい
が、これは不可能である。よつて、ゲル化剤を用いる場
合合もできるだけ少ない使用量でゲル化するゲル形成性
物質を選択することが好ましい。従つて、表−2の結果
から選択すべき条件は、分子量40,000,140,000及び28
0,000のポリアクリル酸ナトリウムを使用した場合であ
る。As described above, the major advantage of the gel type deodorant is that the replacement time can be visually determined. That is, ideally, it is desirable to have no residue at the final stage, but this is not possible. Therefore, when a gelling agent is used, it is preferable to select a gel-forming substance that gels with a use amount as small as possible. Therefore, the conditions to be selected from the results in Table 2 are that the molecular weight is 40,000, 140,000 and 28.
This is the case when 0,000 sodium polyacrylate is used.
実施例2 分子量40,000,140,000及び280,000のポリアクリル酸ナ
トリウムを使用したゲルに表−1に記載した脱臭剤中で
優れた脱臭能力を有したエポリオンN−100を含有さ
せたときのゲル化状態の結果を表−3に示す。かくして
ゲルを形成するゲル化と脱臭剤のゲル内への配合とを同
時に実施した。表−3より明らかなように、脱臭剤の含
有量を多くすると比例的にポリアクリル酸ナトリウム及
びポリエチレングリコールジグリシジルエーテル量も増
加させなければゲル化しなくなる。従つて対象臭気強度
に応じて脱臭剤量を選択し、さらにゲル化条件を選択す
れば目的とするゲル型脱臭剤が得られる。Example 2 The gelation state of gels using sodium polyacrylates having molecular weights of 40,000, 140,000 and 280,000 containing Epolione N-100 having excellent deodorizing ability in the deodorizing agents shown in Table 1 The results are shown in Table-3. Thus, gelling to form a gel and incorporation of a deodorant into the gel were performed simultaneously. As is clear from Table 3, if the content of the deodorant is increased, the gelation will not occur unless the amounts of sodium polyacrylate and polyethylene glycol diglycidyl ether are proportionally increased. Therefore, the target gel-type deodorant can be obtained by selecting the amount of deodorant according to the target odor intensity and further selecting the gelling conditions.
表3において、グリシジルエーテルはポリエチレングリ
コールジグリシジルエーテルを使用したが、これに代え
てエチレングリコールジグリシジルエーテル、ポリプロ
ピレングリコールジグリシジルエーテル、ポリグリセロ
ールポリグリシジルエーテル、グリセロールポリグリシ
ジルエーテルをそれぞれ使用してゲル化状態を観察比較
した結果、いずれの場合もゲル化は良好であつた。 In Table 3, polyethylene glycol diglycidyl ether was used as the glycidyl ether, but instead of this, ethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, polyglycerol polyglycidyl ether, and glycerol polyglycidyl ether were used for gelation. As a result of observing and comparing the states, gelation was good in all cases.
また、ポリアクリル酸ナトリウムに代えてポリアクリル
酸アンモニウムを使用した場合もナトリウム塩とほぼ同
じ挙動を示し、同様なゲル型脱臭剤が得られた。Also, when ammonium polyacrylate was used instead of sodium polyacrylate, the same behavior as the sodium salt was exhibited, and a similar gel-type deodorant was obtained.
実施例3 脱臭能力試験に使用したゲルは、試料NO.5の条件で作
成し2.0gの大きさに切断したものである。試験には500
mlの三角フラスコを用い、フラスコ内に所定の臭気ガス
(アンモニア,トリメチルアミン,硫化水素,メチルメ
ルカプタンの4種を使用)及びゲル型脱臭剤(2.0gを
入れ、時間経過と脱臭率との関係を調べた。試験温度は
4℃(フラスコを冷蔵庫内に放置)、25℃(フラスコ
を室内放置)、50℃(フラスコを恒温槽内に放置)の
三点にて行つた。また、比較品として現在市販されてい
る製品を一点試験に供した。ブランク試験用としては、
表−2中の試料NO.iの条件で作成したゲルを試料NO.5
のゲルと同様に2.0gの大きさに切断したものを使用し
た。Example 3 The gel used in the deodorizing ability test was prepared under the condition of sample No. 5 and cut into a size of 2.0 g. 500 for the exam
Using a Erlenmeyer flask of ml, the odorous gas (ammonia, trimethylamine, hydrogen sulfide, and methyl mercaptan 4 kinds) and gel type deodorant (2.0 g) were put in the flask, and the relationship between the elapsed time and the deodorization rate The test temperature was 4 ° C. (the flask was left in the refrigerator), 25 ° C. (the flask was left indoors), and 50 ° C. (the flask was left in a constant temperature bath). The currently marketed product was subjected to a one-point test.
The gel prepared under the conditions of sample NO.i in Table-2 is sample NO.5.
The gel was cut into a size of 2.0 g in the same manner as the gel.
各臭気ガスに対する脱臭率は次のとおりである。The deodorization rate for each odorous gas is as follows.
アンモニアに対する脱臭率 トリメチルアミンに対する脱臭率 硫化水素に対する脱臭率 メチルメルカプタンに対する脱臭率 以上記載した一連の脱臭試験結果から試料NO.5の脱臭
能力が極めて優れていることがわかる。また、ブランク
品の結果から窒素系臭気はゲル内に吸収され易いが、イ
オウ系臭気は殆んど吸収されないことがわかる。Deodorization rate for ammonia Deodorization rate for trimethylamine Deodorization rate for hydrogen sulfide Deodorization rate for methyl mercaptan From the series of deodorization test results described above, it is understood that the deodorizing ability of Sample No. 5 is extremely excellent. In addition, it can be seen from the result of the blank product that the nitrogen odor is easily absorbed in the gel, but the sulfur odor is hardly absorbed.
実施例4 実施例3で使用した試料NO.5のゲル型脱臭剤を家庭用
冷蔵庫のモニター試験用として選択した。Example 4 The gel type deodorant of Sample No. 5 used in Example 3 was selected for the monitor test of a household refrigerator.
モニター試験条件は次のとおりである。The monitor test conditions are as follows.
(1) 脱臭剤:100gのゲル型脱臭剤をプラスチツク
容器(直径60mm)に入れて密栓し、使用時にフタをと
る。(1) Deodorant: Put 100 g of the gel type deodorant in a plastic container (diameter 60 mm), tightly stopper and remove the lid at the time of use.
(2) 対 象:一般家庭用冷蔵庫(容量200l) (3) 期 間:一ケ月間連続使用 (4) 判定法:主に使用している者(多くの場合主婦)
の官能によつて効果を判定する。殆んどの家庭で何らか
の脱臭剤を冷蔵庫内で使用しているが、試験開始時にそ
れらを除いてもらつた。従つて、効果の判定としてこれ
まで使用していた商品との比較にもなる。(2) Target: Refrigerator for general household (200 l capacity) (3) Period: Continuous use for one month (4) Judgment method: Those who mainly use it (mostly housewives)
The effect is judged by the sensory sensation. Almost all households use some kind of deodorant in the refrigerator, but they were removed at the start of the test. Therefore, it can be compared with the products that have been used so far as the determination of the effect.
(5) 判定基準:a…におわなくなつた〜殆んどにおわ
なくなつた。(効果が顕著に認められる) b…においが軽減された。(5) Judgment Criteria: a ... (The effect is noticeable) b ... The odor was reduced.
(効果が認められる) c…かわらない。(効果なし) d…においが強くなつた。 (Effects are recognized) c. (No effect) d ... The odor was strong.
(逆効果又は以前に使用していた脱臭
剤よりも効果がない) (6) モニター数:30家庭 試験結果を表−4に示す。(Negative effect or less effective than previously used deodorant) (6) Number of monitors: 30 Household test results are shown in Table-4.
表−4の結果より明らかなように、1ケ月後においても
80%以上の家庭で脱臭効果を認めている。 As is clear from the results shown in Table 4, 80% or more of households have a deodorizing effect even after one month.
(発明の効果) 本発明のゲル型脱臭剤は、各種の悪臭に対してすぐれた
脱臭効果を有する化学反応型脱臭剤をゲル内に含有して
いるので、定置型脱臭剤として建築物、交通機関内等の
生活密閉空間ないしは密閉機器内の脱臭に特に有用であ
る。(Effect of the invention) The gel-type deodorant of the present invention contains a chemically reactive deodorant having an excellent deodorizing effect against various malodors in the gel, so that it can be used as a stationary deodorant for buildings, transportation, and the like. It is particularly useful for deodorizing living closed spaces or closed equipment such as in an engine.
Claims (1)
クリル酸ナトリウム又はポリアクリル酸アンモニウムの
2乃至30重量%と、ジグリシジルエーテル又はポリグ
リシジルエーテルの1乃至10重量%と、ベタイン型化
合物を有効成分とする化学反応型脱臭剤の5乃至40重
量%とを含有し、残部が水より成ることを特徴とするゲ
ル型脱臭剤。1. A betaine compound as an active ingredient, 2 to 30% by weight of sodium polyacrylate or ammonium polyacrylate having a molecular weight of 40,000 to 300,000, 1 to 10% by weight of diglycidyl ether or polyglycidyl ether. And 5 to 40% by weight of the chemical reaction type deodorant, wherein the balance is water.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63223627A JPH0642902B2 (en) | 1988-09-08 | 1988-09-08 | Gel type deodorant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63223627A JPH0642902B2 (en) | 1988-09-08 | 1988-09-08 | Gel type deodorant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0271744A JPH0271744A (en) | 1990-03-12 |
| JPH0642902B2 true JPH0642902B2 (en) | 1994-06-08 |
Family
ID=16801172
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63223627A Expired - Fee Related JPH0642902B2 (en) | 1988-09-08 | 1988-09-08 | Gel type deodorant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0642902B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0827601A (en) * | 1994-07-06 | 1996-01-30 | Takeshiyou:Kk | Socks having toes and inhibiting slippage |
-
1988
- 1988-09-08 JP JP63223627A patent/JPH0642902B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0827601A (en) * | 1994-07-06 | 1996-01-30 | Takeshiyou:Kk | Socks having toes and inhibiting slippage |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0271744A (en) | 1990-03-12 |
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