JPH0249745B2 - - Google Patents
Info
- Publication number
- JPH0249745B2 JPH0249745B2 JP62008277A JP827787A JPH0249745B2 JP H0249745 B2 JPH0249745 B2 JP H0249745B2 JP 62008277 A JP62008277 A JP 62008277A JP 827787 A JP827787 A JP 827787A JP H0249745 B2 JPH0249745 B2 JP H0249745B2
- Authority
- JP
- Japan
- Prior art keywords
- deodorant
- polymer electrolyte
- segments
- solution
- production method
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000002781 deodorant agent Substances 0.000 claims description 38
- 239000005518 polymer electrolyte Substances 0.000 claims description 24
- -1 Y 1 Chemical compound 0.000 claims description 9
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 claims description 7
- 229940047670 sodium acrylate Drugs 0.000 claims description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 239000012736 aqueous medium Substances 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- 229920002401 polyacrylamide Polymers 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- VAPQAGMSICPBKJ-UHFFFAOYSA-N 2-nitroacridine Chemical compound C1=CC=CC2=CC3=CC([N+](=O)[O-])=CC=C3N=C21 VAPQAGMSICPBKJ-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims 2
- 239000000243 solution Substances 0.000 description 26
- 238000004519 manufacturing process Methods 0.000 description 17
- 235000019645 odor Nutrition 0.000 description 17
- 239000007864 aqueous solution Substances 0.000 description 12
- 238000010790 dilution Methods 0.000 description 12
- 239000012895 dilution Substances 0.000 description 12
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 230000001877 deodorizing effect Effects 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 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
- 239000000679 carrageenan Substances 0.000 description 3
- 229920001525 carrageenan Polymers 0.000 description 3
- 235000010418 carrageenan Nutrition 0.000 description 3
- 229940113118 carrageenan Drugs 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 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 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052776 Thorium Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- CCJAYIGMMRQRAO-UHFFFAOYSA-N 2-[4-[(2-hydroxyphenyl)methylideneamino]butyliminomethyl]phenol Chemical compound OC1=CC=CC=C1C=NCCCCN=CC1=CC=CC=C1O CCJAYIGMMRQRAO-UHFFFAOYSA-N 0.000 description 1
- JQUWCYSGSDOZOO-UHFFFAOYSA-N 2-methoxypropane-1,2-diol Chemical compound COC(C)(O)CO JQUWCYSGSDOZOO-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229920006322 acrylamide copolymer Polymers 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- BSCJIBOZTKGXQP-UHFFFAOYSA-N n-(2-hydroxyethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCO BSCJIBOZTKGXQP-UHFFFAOYSA-N 0.000 description 1
- UUORTJUPDJJXST-UHFFFAOYSA-N n-(2-hydroxyethyl)prop-2-enamide Chemical compound OCCNC(=O)C=C UUORTJUPDJJXST-UHFFFAOYSA-N 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- LLLCSBYSPJHDJX-UHFFFAOYSA-M potassium;2-methylprop-2-enoate Chemical compound [K+].CC(=C)C([O-])=O LLLCSBYSPJHDJX-UHFFFAOYSA-M 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Description
【発明の詳細な説明】
「産業上の利用分野」
本発明は、生物体からの排出物や生物体自身の
腐敗物等より成る悪臭源に対し、複合塩型の高分
子電解質の呈する作用を利用して消臭効果を達成
する消臭剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION "Field of Industrial Application" The present invention utilizes the effect of a complex salt type polymer electrolyte on sources of bad odors consisting of excreta from living organisms and decayed matter of the living organisms themselves. This invention relates to a deodorizing agent that can be used to achieve a deodorizing effect.
「従来の技術」
消臭剤は、上述した悪臭源を多量に有する便
所、養豚場、養鶏場、畜舎、生鮮食料品市場のゴ
ミ箱はもとより、一般家庭に於ける台所、冷蔵
庫、ペツト用具や、人体からの発生物に関係する
靴及び靴下類、或いは浴室及び自動車内部等で発
生する悪臭、異臭を封じるために広く使用されて
いる。``Prior Art'' Deodorizers can be used not only in toilets, pig farms, poultry farms, livestock sheds, and garbage cans at fresh food markets, but also in kitchens, refrigerators, pet utensils, It is widely used to seal out bad odors and foreign odors that occur in shoes and socks related to human body products, as well as in bathrooms and inside automobiles.
従来より知られているこの種の消臭剤として
は、無機物である活性炭の界面吸着力を利用した
ものがあり、また近年、鉄イオンと糖の間の酸化
還元反応を利用したものが報告されている。 Conventionally known deodorants of this type include those that utilize the interfacial adsorption power of activated carbon, which is an inorganic substance, and in recent years, deodorants that utilize the redox reaction between iron ions and sugar have been reported. ing.
一方有機物では、ポリアクリルアミドを使用す
るもの(特公昭61−7828号公報)、アクリル酸ナ
トリウム・アクリルアミドコポリマーを使用する
もの(特公昭61−7829号公報)、更には、アクリ
ル酸ナトリウム(モノマー)を使用するもの(特
公昭60−13702号公報)等の発明も提案されてい
る。 On the other hand, organic materials include those that use polyacrylamide (Japanese Patent Publication No. 61-7828), sodium acrylate/acrylamide copolymer (Japanese Patent Publication No. 61-7829), and even sodium acrylate (monomer). Inventions such as those using the same method (Japanese Patent Publication No. 60-13702) have also been proposed.
「発明が解決しようとする問題点」
処で、悪臭源、異臭源を化学的に探査すると、
含イオウ化合物と含窒素化合物とに大略分類さ
れ、そのうち、特に酸性の二酸化イオウと塩基性
のアンモニアに原因することが圧倒的に多い。``Problems to be solved by the invention'' Now, when we chemically investigate the source of bad odors and off-odors,
It is roughly classified into sulfur-containing compounds and nitrogen-containing compounds, and of these, acidic sulfur dioxide and basic ammonia are overwhelmingly responsible.
しかしながら、従来技術による各種の消臭剤
は、前記した悪臭、異臭の抑止に対して全く効果
を示さないか、或いは極めて短時間しか有効では
なく、また、酸性か塩基性の何れか一方にしか効
力がなく、人間生活を快適ならしめるための消臭
剤として満足できる貢献は果していなかつた。 However, various deodorants according to the prior art are either not effective at all in suppressing the above-mentioned bad odors and foreign odors, or are only effective for a very short period of time, and are only effective against either acidic or basic odors. It was ineffective and had not made a satisfactory contribution as a deodorant to make human life more comfortable.
本発明は、上述した従来の欠点、不都合を解消
するべく創案された消臭剤であつて、悪臭源、異
臭源が酸性であると塩基性であるとを問わず、長
時間にわたつて消臭効果を持続させるようにする
ことを目的とするものである。 The present invention is a deodorizing agent devised to eliminate the above-mentioned conventional drawbacks and inconveniences, and is a deodorizing agent that can be used to eliminate malodors and foreign odors for a long period of time, regardless of whether they are acidic or basic. The purpose is to make the odor effect last.
「問題点を解決するための手段」及び「作用」
本発明の消臭剤は、高分子反応について研究を
行つた結果得られたものであつて、活性水素を有
する基をもつノニオン性モノマーに由来するセグ
メントと、カルボン酸カリウムを連結するモノマ
ーに由来するセグメントと、カルボン酸トリウム
を連結するモノマーに由来するセグメントとを同
時に含む高重合度の複合塩型高分子電解質を、水
系媒体に溶解させたものであり、この消臭剤を悪
臭、異臭を放つ場所に静置、散布若しくは注入す
ると、臭が直ちに消え、しかも酸性、塩基性を問
わず、長時間にわたつて消臭効果が持続する。"Means for Solving the Problems" and "Actions" The deodorant of the present invention was obtained as a result of research on polymer reactions, and is based on nonionic monomers having active hydrogen-containing groups. A complex salt type polymer electrolyte with a high degree of polymerization that simultaneously contains a segment derived from a monomer that connects potassium carboxylate, a segment derived from a monomer that connects thorium carboxylate, and a segment derived from a monomer that connects thorium carboxylate is dissolved in an aqueous medium. When this deodorant is left standing, sprayed, or injected into a place emitting a bad odor, the odor disappears immediately, and the deodorizing effect lasts for a long time regardless of whether it is acidic or basic. .
即ち本発明は、水系媒体に対して次の一般式
にて表される複合塩型高分子電解質
(但し、X1、X2、X3及びX4は、水素若しくはメ
チル基であり、Y1、Y2、Y3及びY4は水素、ヒド
ロキシメチル基若しくはヒドロキシエチル基であ
り、0.0099≦a≦0.4999、0.0001≦b≦0.25で、
しかも0.01≦a+b≦0.5、また、0≦c≦0.99、
0≦d≦0.99で、しかも0.5≦c+d≦0.99で、且
つa+b+c+d=1であり、10000≦n≦
300000である)
を有効成分として含有せしめた消臭剤であり、上
記した所定の高分子電解質のもつイオン化傾向の
相違と、イオン反撥力の緩和作用を含めた独特の
溶解形態が、悪臭、異臭を放つ酸性物質若しくは
塩基性物質を取り込んで補促し、次いで高分子反
応を行つて無臭なものへと変化させる作用機構を
もたらしている。 That is, the present invention provides a composite salt type polymer electrolyte represented by the following general formula for an aqueous medium. (However, X 1 , X 2 , X 3 and X 4 are hydrogen or methyl groups, Y 1 , Y 2 , Y 3 and Y 4 are hydrogen, hydroxymethyl group or hydroxyethyl group, and 0.0099≦a ≦0.4999, 0.0001≦b≦0.25,
Moreover, 0.01≦a+b≦0.5, and 0≦c≦0.99,
0≦d≦0.99, and 0.5≦c+d≦0.99, and a+b+c+d=1, and 10000≦n≦
300,000) as an active ingredient, and the difference in ionization tendency of the above-mentioned specified polymer electrolytes and the unique dissolution form including the moderating effect of ion repulsion force eliminates bad odors and foreign odors. The mechanism of action is to take in acidic or basic substances that emit , supplement them, and then undergo a polymer reaction to transform them into odorless substances.
ここで、所定の高分子電解質に関連して、一般
式中のbが0.0001未満及び0.25より大きい場合
には、イオン化傾向の相違を充分に発揮できず、
また、a+bが0.01未満である場合には、悪臭、
異臭の成分と反応する効力が弱く、何れの場合に
も消臭効果及びその持続性が著しく低下する。 Here, in relation to a given polymer electrolyte, if b in the general formula is less than 0.0001 and greater than 0.25, the difference in ionization tendency cannot be fully exhibited,
In addition, if a+b is less than 0.01, bad odor,
The effectiveness of reacting with off-odor components is weak, and in either case, the deodorizing effect and its sustainability are significantly reduced.
一方、c+dが0.5未満である場合には、同一
鎖内でのイオン反撥を緩和する力が弱くなり、悪
臭、異臭の成分の補促に対して不向きとなる。 On the other hand, if c+d is less than 0.5, the power to alleviate ion repulsion within the same chain will be weak, making it unsuitable for supplementing malodor and off-odor components.
更に、nが10000未満及び300000より大きい場
合には、水系媒体中で適切な溶解形態を呈し得
ず、従つて悪臭、異臭の成分を取り込む能力が著
しく欠けてしまうので、好ましくない。 Furthermore, if n is less than 10,000 or greater than 300,000, it is not preferable because it will not be able to exhibit an appropriate dissolved form in an aqueous medium, and therefore the ability to take in malodorous and off-odor components will be significantly lacking.
「調整」
本発明の消臭剤は、アクリルアミド、N―ヒド
ロキシメチルアクリルアミド、N・N―ジ(ヒド
ロキシメチル)アクリルアミド、N―ヒドロキシ
エチルアクリルアミド、N・N―ジ(ヒドロキシ
エチル)アクリルアミド、メタクリルアミド、N
―ヒドロキシメチルメタクリルアミド、N・N―
ジ(ヒドロキシメチル)メタクリルアミド、N―
ヒドロキシエチルメタクリルアミド、N・N―ジ
(ヒドロキシエチル)メタクリルアミドのホモポ
リマー若しくはコポリマーを水中で水酸化カリウ
ム及び水酸化ナトリウムと接触させて、部分加水
分解させるか(製法1)、または、上述のモノマ
ーのうちの1種若しくは2種と、アクリル酸カリ
ウム、メタクリル酸カリウムのうちの1種及びア
クリル酸ナトリウム、メタクリル酸ナトリウムの
うちの1種とを水中で共重合させること(製法
2)により得られる所定の高分子電解質の水容液
を、適切な濃度に調整した後、使用する。"Adjustment" The deodorant of the present invention contains acrylamide, N-hydroxymethylacrylamide, N.N-di(hydroxymethyl)acrylamide, N-hydroxyethylacrylamide, N.N-di(hydroxyethyl)acrylamide, methacrylamide, N
-Hydroxymethylmethacrylamide, N・N-
Di(hydroxymethyl)methacrylamide, N-
A homopolymer or copolymer of hydroxyethyl methacrylamide, N.N-di(hydroxyethyl) methacrylamide is brought into contact with potassium hydroxide and sodium hydroxide in water to cause partial hydrolysis (Production method 1), or Obtained by copolymerizing one or two of the monomers with one of potassium acrylate, potassium methacrylate, and one of sodium acrylate and sodium methacrylate in water (Production method 2). An aqueous solution of a given polymer electrolyte is adjusted to an appropriate concentration before use.
また更には、メチルアルコール、エチルアルコ
ール、N―プロピルアルコール、イソプロピルア
ルコール、アセトン、ジオキサン等の親水性共沸
溶媒を共存させたり、グリコールエーテル、グリ
セリン等の潤滑剤やセルロース、多糖類等の増粘
剤、ゲル化剤等を混入させることもあり得る。 Furthermore, hydrophilic azeotropic solvents such as methyl alcohol, ethyl alcohol, N-propyl alcohol, isopropyl alcohol, acetone, and dioxane may coexist, lubricants such as glycol ether and glycerin, and thickeners such as cellulose and polysaccharides. Agents, gelling agents, etc. may also be mixed.
尚、所望により、殺菌剤、防腐剤等を添加する
ことは、一向に差し仕えない。 Incidentally, if desired, it is not a problem to add a bactericide, a preservative, etc.
「実施例」
以下、実施例によつて本発明の消臭剤並びに消
臭試験結果を示す。"Example" Hereinafter, the deodorant of the present invention and the results of a deodorizing test will be shown in Examples.
実施例 1
製法1により得た下記構造の高分子電解質の
0.1%水溶液を作成し(20℃に於ける溶液粘度;
750cp、PH8.6)、その200倍稀釈液を消臭剤とし
た。Example 1 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.1% aqueous solution (solution viscosity at 20℃;
750cp, PH8.6), and its 200-fold dilution was used as a deodorant.
実施例 2
製法1により得た下記構造の高分子電解質の
0.08%水溶液を作成し(20℃に於ける溶液粘度;
1000cp、PH8.5)、その200倍稀釈液を消臭剤とし
た。 Example 2 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.08% aqueous solution (solution viscosity at 20℃;
1000cp, PH8.5), and its 200-fold dilution was used as a deodorant.
実施例 3
製法1により得た下記構造の高分子電解質の
0.25%(水:エチルアルコール=90wt%;10wt
%)溶液を作成し(20℃に於ける溶液粘度;
850cp、PH9.8)、その500倍稀釈液を消臭剤とし
た。 Example 3 Polymer electrolyte with the following structure obtained by Production Method 1
0.25% (water: ethyl alcohol = 90wt%; 10wt
%) solution was prepared (solution viscosity at 20℃;
850cp, PH9.8), and its 500-fold dilution was used as a deodorant.
実施例 4
製法1により得た下記構造の高分子電解質の
0.05%(水:ジオキサン=95wt%:5wt%)溶液
を作成し(20℃に於ける溶液粘度;900cp、PH
9.6)、その100倍稀釈液を消臭剤とした。 Example 4 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.05% (water: dioxane = 95wt%: 5wt%) solution (solution viscosity at 20℃: 900cp, PH
9.6), and its 100-fold dilution was used as a deodorant.
実施例 5
製法1により得た下記構造の高分子電解質の
0.3%(水:アセトン=90wt%:10wt%)溶液を
作成し(20℃に於ける溶液粘度;580cp、PH6.1)、
その500倍稀釈液を消臭剤とした。 Example 5 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.3% (water: acetone = 90wt%: 10wt%) solution (solution viscosity at 20°C: 580cp, PH6.1),
A 500-fold diluted solution was used as a deodorant.
実施例 6
製法1により得た下記構造の高分子電解質の
0.08%水溶液を作成し(20℃に於ける溶液粘度;
1150cp、PH6.0)、その150倍稀釈液を消臭剤とし
た。 Example 6 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.08% aqueous solution (solution viscosity at 20℃;
1150cp, PH6.0), and its 150-fold dilution was used as a deodorant.
実施例 7
製法1により得た下記構造の高分子電解質の
0.1%(水:グリセリン=97wt%:3wt%)溶液
を作成し(20℃に於ける溶液粘度;800cp、PH
8.5)、その200倍稀釈液を消臭剤とした。 Example 7 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.1% (water: glycerin = 97wt%: 3wt%) solution (solution viscosity at 20℃: 800cp, PH
8.5), and a 200-fold diluted solution was used as a deodorant.
実施例 8
製法1により得た下記構造の高分子電解質の
0.07%水溶液を作成し(20℃に於ける溶液粘度;
1150cp、PH9.5)、その150倍稀釈液を消臭剤とし
た。 Example 8 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.07% aqueous solution (solution viscosity at 20℃;
1150cp, PH9.5), and its 150-fold dilution was used as a deodorant.
実施例 9
製法1により得た下記構造の高分子電解質の
0.1%(水:モノメトキシプロピレングリコール
=88wt%:12wt%)溶液を作成し(20℃に於け
る溶液粘度;600cp、PH9.6)、その200倍稀釈液を
消臭剤とした。 Example 9 Polymer electrolyte with the following structure obtained by Production Method 1
A 0.1% (water: monomethoxypropylene glycol = 88wt%: 12wt%) solution was prepared (solution viscosity at 20°C: 600cp, PH9.6), and a 200-fold dilution thereof was used as a deodorant.
実施例 10
製法1により得た下記構造の高分子電解質の
0.2%水溶液を作成し(20℃に於ける溶液粘度;
1000cp、PH6.2)、その350倍稀釈液を消臭剤とし
た。 Example 10 Polymer electrolyte with the following structure obtained by Production Method 1
Create a 0.2% aqueous solution (solution viscosity at 20℃;
1000cp, PH6.2), and its 350-fold dilution was used as a deodorant.
実施例 11
製法2により得た下記構造の高分子電解質の
0.1%水溶液を作成し(20℃に於ける溶液粘度;
1030cp、PH8.5)、その200倍稀釈液を消臭剤とし
た。 Example 11 Polymer electrolyte with the following structure obtained by production method 2
Create a 0.1% aqueous solution (solution viscosity at 20℃;
1030cp, PH8.5), and its 200-fold dilution was used as a deodorant.
実施例 12
製法2により得た下記構造の高分子電解質の
0.09%(水:イソプロピルアルコール=93wt%:
7wt%)溶液を作成し(20℃に於ける溶液粘度;
1080cp、PH6.0)、その200倍稀釈液を消臭剤とし
た。 Example 12 Polymer electrolyte with the following structure obtained by production method 2
0.09% (water: isopropyl alcohol = 93wt%:
7wt%) solution (solution viscosity at 20℃;
1080cp, PH6.0), and its 200-fold dilution was used as a deodorant.
実施例 13
製法2により得た下記構造の高分子電解質の
0.2%(水:グリセリン=95wt%:5wt%)溶液
を作成し(20℃に於ける溶液粘度;740cp、PH
9.3)、その400倍稀釈液を消臭剤とした。 Example 13 Polymer electrolyte with the following structure obtained by production method 2
Create a 0.2% (water: glycerin = 95wt%: 5wt%) solution (solution viscosity at 20℃: 740cp, PH
9.3), and a 400-fold diluted solution was used as a deodorant.
実施例 14
製法2により得た下記構造の高分子電解質の
0.1%水溶液を作成し(20℃に於ける溶液粘度;
800cp、PH8.5)、その200倍稀釈液を消臭剤とし
た。 Example 14 Polymer electrolyte with the following structure obtained by production method 2
Create a 0.1% aqueous solution (solution viscosity at 20℃;
800cp, PH8.5), and its 200-fold dilution was used as a deodorant.
実施例 15
製法2により得た下記構造の高分子電解質の
0.1%(水:エチルアルコール=93wt%;7wt%)
溶液を作成し(20℃に於ける溶液粘度;570cp、
PH8.8)、その200倍稀釈液を消臭剤とした。 Example 15 Polymer electrolyte with the following structure obtained by production method 2
0.1% (water: ethyl alcohol = 93wt%; 7wt%)
Create a solution (solution viscosity at 20℃; 570cp,
PH8.8), and its 200-fold dilution was used as a deodorant.
実施例 16
実施例1で製造した液状消臭剤100部に対して、
天然水溶性高分子のカラギーナンAFT−70−1
(但し、タカラゲン株式会社製品)を2.5部添加し
て均一に混合し、ゲル状消臭剤とした。 Example 16 For 100 parts of the liquid deodorant produced in Example 1,
Natural water-soluble polymer carrageenan AFT-70-1
(However, 2.5 parts of Takaragen Co., Ltd. product) was added and mixed uniformly to form a gel deodorant.
実施例 17
実施例2で製造した液状消臭剤100部に対して、
実施例16で使用したカラギーナンAFT−70−1
を2部添加して均一に混合し、ゲル状消臭剤とし
た。Example 17 For 100 parts of the liquid deodorant produced in Example 2,
Carrageenan AFT-70-1 used in Example 16
2 parts were added and mixed uniformly to obtain a gel deodorant.
実施例 18
実施例11で製造した液状消臭剤100部に対して、
実施例16で使用したカラギーナンAFT−70−1
を3部添加して均一に混合し、ゲル状消臭剤とし
た。Example 18 For 100 parts of the liquid deodorant produced in Example 11,
Carrageenan AFT-70-1 used in Example 16
3 parts were added and mixed uniformly to obtain a gel deodorant.
実施例 19
上部に開閉コツクを取り付けた500ml用三角フ
ラスコに、実施例1〜15で製造した消臭剤を200
mlずつ、及び実施例16〜18で製造したゲル状消臭
剤を2×2×2cm3ずつ、各々計り取つた後、コツ
クを開いて、別途用意した二酸化イオウを
200ppm含んだ空気2を1/minの流量で接
触させ続け、北川式検知管法によつて経過時間毎
の二酸化イオウの減衰率を測定した。Example 19 200ml of the deodorant produced in Examples 1 to 15 was placed in a 500ml Erlenmeyer flask with an opening/closing cap attached to the top.
After measuring out 1 ml and 2 x 2 x 2 cm 3 of the gel deodorant produced in Examples 16 to 18, open the container and pour in the separately prepared sulfur dioxide.
Air 2 containing 200 ppm was kept in contact at a flow rate of 1/min, and the decay rate of sulfur dioxide was measured at each elapsed time using the Kitagawa detector tube method.
更に、一度測定に使用した消臭剤試料をそのま
まにしたうえで、新たに二酸化イオウを200ppm
含んだ空気を接続し、繰り返し試験を行つて、消
臭効果の持続性を調べた。 Furthermore, while leaving the deodorant sample used for the measurement as it was, we added 200ppm of sulfur dioxide.
The durability of the deodorizing effect was examined by connecting air containing air and conducting repeated tests.
また、比較試料として下記の3種類の水溶液を
選択し、同様の試験に供した。結果を第1図に示
す。 In addition, the following three types of aqueous solutions were selected as comparative samples and subjected to similar tests. The results are shown in Figure 1.
比較試料……アクリル酸ナトリウムを10ppm
含む水溶液。 Comparison sample...sodium acrylate 10ppm
Aqueous solution containing.
比較試料……平均重合度200000のポリアクリ
ルアミドを10ppm含む水溶液。 Comparative sample: an aqueous solution containing 10 ppm of polyacrylamide with an average degree of polymerization of 200,000.
比較試料……アクリル酸ナトリウムセグメン
ト25%とアクリルアミドセグメント75%より成る
コポリマーを10ppm含む水溶液。 Comparative sample: an aqueous solution containing 10 ppm of a copolymer consisting of 25% sodium acrylate segments and 75% acrylamide segments.
実施例 20
実施例19と同様の方法により、実施例1〜18で
製造した本発明の消臭剤の所定量に対して、アン
モニアを200ppm含んだ空気2を接触させ続け、
経過時間毎のアンモニアの減衰率を測定した。Example 20 By the same method as in Example 19, air 2 containing 200 ppm of ammonia was kept in contact with a predetermined amount of the deodorant of the present invention produced in Examples 1 to 18,
The decay rate of ammonia was measured for each elapsed time.
また、比較試料も実施例19で使用した比較試料
、、を選択し、同様の試験に供した。結果
を第2図に示す。 In addition, the comparative sample used in Example 19 was also selected and subjected to the same test. The results are shown in Figure 2.
以上により、本発明の消臭剤が強力且つ持続性
のある性能を堅持し、しかも臭い源の種類に依ら
ず、有効であることが確認された。 From the above, it was confirmed that the deodorant of the present invention maintains strong and long-lasting performance and is effective regardless of the type of odor source.
第1図は、実施例19に於ける測定の結果判明し
た本発明の消臭剤との接触による二酸化イオウ
(酸性臭源)含量の減衰率を示す表である。第2
図は、実施例20に於ける測定の結果判明した本発
明の消臭剤との接触によるアンモニア(塩基性臭
源)含量の減衰率を示す表である。
FIG. 1 is a table showing the attenuation rate of sulfur dioxide (acidic odor source) content due to contact with the deodorant of the present invention, which was found as a result of measurements in Example 19. Second
The figure is a table showing the attenuation rate of ammonia (basic odor source) content due to contact with the deodorant of the present invention, which was found as a result of measurements in Example 20.
Claims (1)
高分子電解質 (但し、X1、X2、X3及びX4は、水素若しくはメ
チル基であり、Y1、Y2、Y3及びY4は水素、ヒド
ロキシメチル基若しくはヒドロキシエチル基であ
り、0.0099≦a≦0.4999、0.0001≦b≦0.25で、
しかも0.01≦a+b≦0.5、また、0≦c≦0.99、
0≦d≦0.99で、しかも0.5≦c+d≦0.99で、且
つa+b+c+d=1であり、10000≦n≦
300000である) を有効成分として含有させることを特徴とする消
臭剤。 2 一般式にて表される高分子電解質が、平均
重合度200000のポリアクリルアミドを加水分解さ
せて得る、アクリル酸カリウムセグメント20%、
アクリル酸ナトリウムセグメント5%、及びアク
リルアミドセグメント75%より成る共重合体であ
る特許請求の範囲1に記載の消臭剤。 3 一般式にて表される高分子電解質が、平均
重合度300000のポリアクリルアミドを加水分解さ
せて得る、アクリル酸カリウムセグメント10%、
アクリル酸ナトリウムセグメント10%、及びアク
リルアミドセグメント80%より成る共重合体であ
る特許請求の範囲1に記載の消臭剤。[Claims] 1. A complex salt type polymer electrolyte represented by the general formula in an aqueous medium (However, X 1 , X 2 , X 3 and X 4 are hydrogen or methyl groups, Y 1 , Y 2 , Y 3 and Y 4 are hydrogen, hydroxymethyl group or hydroxyethyl group, and 0.0099≦a ≦0.4999, 0.0001≦b≦0.25,
Furthermore, 0.01≦a+b≦0.5, and 0≦c≦0.99,
0≦d≦0.99, 0.5≦c+d≦0.99, and a+b+c+d=1, and 10000≦n≦
300,000) as an active ingredient. 2. The polymer electrolyte represented by the general formula contains 20% potassium acrylate segments obtained by hydrolyzing polyacrylamide with an average degree of polymerization of 200000,
The deodorant according to claim 1, which is a copolymer consisting of 5% sodium acrylate segments and 75% acrylamide segments. 3 The polymer electrolyte represented by the general formula is 10% potassium acrylate segment obtained by hydrolyzing polyacrylamide with an average degree of polymerization of 300000,
The deodorant according to claim 1, which is a copolymer consisting of 10% sodium acrylate segments and 80% acrylamide segments.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62008277A JPS63177859A (en) | 1987-01-19 | 1987-01-19 | Deodorant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62008277A JPS63177859A (en) | 1987-01-19 | 1987-01-19 | Deodorant |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63177859A JPS63177859A (en) | 1988-07-22 |
JPH0249745B2 true JPH0249745B2 (en) | 1990-10-31 |
Family
ID=11688682
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62008277A Granted JPS63177859A (en) | 1987-01-19 | 1987-01-19 | Deodorant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63177859A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0683721B2 (en) * | 1989-07-07 | 1994-10-26 | ジョンソン株式会社 | Preparation method of air volatile concentrated composition and air volatile agent |
JP4004703B2 (en) * | 1999-03-01 | 2007-11-07 | 花王株式会社 | Deodorant composition |
JP5132073B2 (en) * | 2006-03-31 | 2013-01-30 | 小林製薬株式会社 | Hydrous gel |
JP5068030B2 (en) * | 2006-03-31 | 2012-11-07 | 小林製薬株式会社 | A collection of gel-like molded bodies |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54157834A (en) * | 1978-06-01 | 1979-12-13 | Nonchi Kk | Liquid deodorant |
JPS54157835A (en) * | 1978-06-02 | 1979-12-13 | Nonchi Kk | Liquid deodorant |
JPS6013702A (en) * | 1983-07-04 | 1985-01-24 | Ube Ind Ltd | Fungicide for soil |
JPS617828A (en) * | 1984-06-22 | 1986-01-14 | Canon Inc | Driving method of liquid-crystal element |
JPS617829A (en) * | 1984-06-22 | 1986-01-14 | Canon Inc | Driving method of liquid-crystal element |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6013702B2 (en) * | 1978-05-31 | 1985-04-09 | 東 川副 | liquid deodorant |
JPS54160737A (en) * | 1978-06-05 | 1979-12-19 | Nonchi Kk | Liquid deodorant |
JPS54160738A (en) * | 1978-06-05 | 1979-12-19 | Nonchi Kk | Liquid deodorant |
-
1987
- 1987-01-19 JP JP62008277A patent/JPS63177859A/en active Granted
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54157834A (en) * | 1978-06-01 | 1979-12-13 | Nonchi Kk | Liquid deodorant |
JPS54157835A (en) * | 1978-06-02 | 1979-12-13 | Nonchi Kk | Liquid deodorant |
JPS6013702A (en) * | 1983-07-04 | 1985-01-24 | Ube Ind Ltd | Fungicide for soil |
JPS617828A (en) * | 1984-06-22 | 1986-01-14 | Canon Inc | Driving method of liquid-crystal element |
JPS617829A (en) * | 1984-06-22 | 1986-01-14 | Canon Inc | Driving method of liquid-crystal element |
Also Published As
Publication number | Publication date |
---|---|
JPS63177859A (en) | 1988-07-22 |
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