JPS62299266A - Washable deodorizing body and its production - Google Patents
Washable deodorizing body and its productionInfo
- Publication number
- JPS62299266A JPS62299266A JP61142845A JP14284586A JPS62299266A JP S62299266 A JPS62299266 A JP S62299266A JP 61142845 A JP61142845 A JP 61142845A JP 14284586 A JP14284586 A JP 14284586A JP S62299266 A JPS62299266 A JP S62299266A
- Authority
- JP
- Japan
- Prior art keywords
- deodorizing
- deodorant
- clathrate
- polyurethane
- deodorizing body
- 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
- 230000001877 deodorizing effect Effects 0.000 title claims description 29
- 238000004519 manufacturing process Methods 0.000 title description 6
- 239000002781 deodorant agent Substances 0.000 claims description 25
- 229920002635 polyurethane Polymers 0.000 claims description 18
- 239000004814 polyurethane Substances 0.000 claims description 18
- 239000000843 powder Substances 0.000 claims description 12
- 238000005187 foaming Methods 0.000 claims description 8
- 239000000835 fiber Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 description 25
- 239000007789 gas Substances 0.000 description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 9
- 235000019645 odor Nutrition 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000004745 nonwoven fabric Substances 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000004332 deodorization Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 238000006757 chemical reactions by type Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005108 dry cleaning Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 229920000858 Cyclodextrin Polymers 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000003113 dilution method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000012770 industrial material Substances 0.000 description 2
- 239000011325 microbead Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 235000015178 Asplenium bulbiferum subsp bulbiferum Nutrition 0.000 description 1
- 244000178908 Asplenium bulbiferum subsp bulbiferum Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 208000008454 Hyperhidrosis Diseases 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- -1 copper and aluminum Chemical compound 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 210000003000 inclusion body Anatomy 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 150000002506 iron compounds Chemical class 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 239000012229 microporous material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000010813 municipal solid waste Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229920006284 nylon film Polymers 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920006264 polyurethane film Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 208000013460 sweaty Diseases 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
3、発明の詳細な説明コ
本発明は、新規消臭体とその製造法に関し、特に速効性
と持続性に富み、耐洗濯性のある消臭体とその製造法に
関するものである。[Detailed Description of the Invention] 3. Detailed Description of the Invention The present invention relates to a novel deodorizing body and a method for manufacturing the same, and in particular, a deodorizing body that is fast-acting, long-lasting, and wash-resistant, and a method for manufacturing the same. It is related to.
我々を取りまく生活環境には多くの悪臭源があり不快感
や嫌悪感を与えている。There are many sources of bad odors in the living environment that surround us, giving us discomfort and disgust.
この悪臭は騒音、振動と共に従来より三大公害と称され
、重大な感心が持たれており積極的に排除しようと法的
規制も行われている。しかしながらこれらは現実の小さ
な身のまわりの生活環境にまで浸透したものではない。This odor, along with noise and vibration, has traditionally been referred to as one of the three major pollutions, and is viewed with great concern, and legal regulations are being put in place to actively eliminate it. However, these have not yet penetrated into the actual living environment around us.
本発明は広義の公害的悪臭から家庭内で発生する小さな
悪臭をも消滅せしめることを意図して行ったものである
。The present invention was carried out with the intention of eradicating even small odors generated in the home from the nuisance odors in a broad sense.
一般に悪臭を消滅させることを通常脱臭もしくは消臭と
表現しているが、広義には同一意味と解しここでは消臭
と呼ぶことにする。In general, the elimination of bad odors is usually expressed as deodorization or deodorization, but in a broader sense, they are interpreted to have the same meaning, so we will call them deodorization here.
現在、身のまわりにある奥を観察してみると、汗くさい
下着、くっ下、寝具、タバコの臭いのする上着、おむつ
、シーツ、押入れ、下駄箱、ロッカー、会議室、トイレ
、冷蔵庫、ゴミ箱、ペット飼育器、どぶ等無数に存在す
る。If you look at the inner parts of your everyday life, you will find sweaty underwear, socks, bedding, jackets that smell like cigarettes, diapers, sheets, closets, shoe cabinets, lockers, meeting rooms, toilets, refrigerators, etc. There are countless trash cans, pet cages, gutters, etc.
従来よりこれらの臭気を除去する最も一般的な方法とし
て活性炭による吸着法がある。この粉状木炭である活性
炭は取扱上の制約があり、水分を吸収するとその効力を
消失するなど使用上にも制約がある。Conventionally, the most common method for removing these odors is the adsorption method using activated carbon. Activated carbon, which is powdered charcoal, has restrictions in its handling, and there are also restrictions in its use, such as its effectiveness disappearing when it absorbs moisture.
この様な状況の中にあって、臭いの化学的成分の究明が
進んでこれに対応した新しい消臭方法が見出されている
。即ち、その機構上から分類すると、(1)吸着除去す
る方法、(2)分解除去する方法、(3)化学反応で無
臭化する方法。更に使用する形態上から分類すると、(
1) エアゾールタイプ、(2)液状タイプ、(3)
粉末顆粒タイプ等になる。Under these circumstances, research into the chemical components of odors has progressed, and new deodorizing methods have been discovered. That is, when classified based on the mechanism, (1) a method of adsorption and removal, (2) a method of decomposition and removal, and (3) a method of deodorization by chemical reaction. If further classified based on the form of use, (
1) Aerosol type, (2) Liquid type, (3)
It comes in powder granule type, etc.
これらの組合せにより目的に応じた消臭剤もしくは消臭
体が作られる。ここで消臭剤とは、消臭する成分を別の
気体、液体、固体物質で稀釈し単独の形態で使用するの
に対し、消臭体とは、これらの形態の消臭剤を例えば繊
維状物質、プラスチックシート状物に支持固定した形態
で使用すると定義されるべきものである。By combining these, deodorants or deodorizing bodies can be created depending on the purpose. Here, a deodorant is a deodorizing component that is diluted with another gas, liquid, or solid substance and used in a single form, whereas a deodorizer is a deodorizer that uses these forms, such as fibers. It should be defined as being used in the form of being supported and fixed on a plastic sheet-like material.
先述の如く、消臭剤と言えば活性炭と言われるほど工業
的資材、家庭内用品に浸透し使用されてきた。As mentioned above, activated carbon has become so pervasive in industrial materials and household products that it is often referred to as a deodorant.
工業的資材として用いる時にはその使用量も多く再生利
用することが常識化しているが、家庭内用品においては
このような概念は皆無に等しがった。When used as an industrial material, it has become common knowledge to use a large amount and recycle it, but this concept has completely disappeared when it comes to household products.
本発明者らは、消臭剤のより優れた利用方法を開発すべ
く鋭意検討した結果、消臭剤自体の有する速効性を損な
うことなく、持続性、耐洗濯性に優れ容易に再生利用で
きる効果の顕著な消臭体と、その製造法の開発に成功し
、本発明に到達した。As a result of intensive studies to develop a better method for using deodorants, the inventors of the present invention found that the deodorant itself has excellent durability and washing resistance, and can be easily recycled without sacrificing its fast-acting properties. We have succeeded in developing a highly effective deodorizing body and a method for producing it, and have arrived at the present invention.
即ち本発明による消臭体は、ゲストが消臭剤であろ包接
物を分散担持してなるポリウレタン多孔質皮膜層を支持
体上に設けたものであり、ゲストが消臭剤である包接物
を粉末状でボリウレクン樹脂溶液に混入分散しこれを支
持体に塗布して後、脱溶媒処理或は発泡処理をして多孔
質皮V層を形成させろことにより好ましく製造される。That is, the deodorizing body of the present invention has a polyurethane porous film layer dispersing and carrying clathrates, whether the guest is a deodorant or not, on a support. It is preferably produced by mixing and dispersing the powder in a Polyurekne resin solution, applying this to a support, and then performing a solvent removal treatment or a foaming treatment to form a porous skin V layer.
本発明で用いろ消臭剤は、適宜公知の消臭剤から選択さ
れろ。消臭剤はゲストとして包接物を形成し得るもので
あれば先述のいずれの81構に属するものでもよいが、
化学反応タイプの消臭剤が最も好ましい。この化学反応
タイプと(ま、中和、酸化、付加、縮合等化学の分野で
定義されている諸反応であり、鉄化合物、アルミ化合物
、樹木抽出物、茶抽出物等、種々の消臭剤が知られてい
る。The deodorant used in the present invention may be appropriately selected from known deodorants. Deodorants may belong to any of the 81 categories mentioned above as long as they can form inclusions as guests.
Chemical reaction type deodorants are most preferred. This chemical reaction type (well, it is a reaction defined in the field of chemistry such as neutralization, oxidation, addition, condensation, etc.), and various deodorants such as iron compounds, aluminum compounds, tree extracts, tea extracts, etc. It has been known.
また、該化学反応タイプは、吸着除去タイプ、分解除去
タイプと組合せて使用できる特徴もあり、消臭能力、安
定性、使い易さ等の効果と共に組合せ使用による利用範
囲の拡大効果も有する。活性炭等の併用は、消臭力を高
めるために通常好ましい。In addition, the chemical reaction type has the characteristic that it can be used in combination with the adsorption removal type and the decomposition removal type, and has the effect of expanding the range of use by using the combination as well as having effects such as deodorizing ability, stability, and ease of use. The combined use of activated carbon or the like is usually preferred in order to enhance the deodorizing power.
本発明では消臭剤をゲスト化合物として包接物の形でポ
リウレタンと組合せることを本質とするが、包接物を形
成する一方の成分であるホスト化合物も適宜公知の包接
物形成性のホスト化合物から進択される。具体例として
は結晶セルローズ、サイクロデキストリン、シリカマイ
クロビーズ、アクリルバルーン
μの孔径を有し包接したゲスト化合物が水や溶剤によっ
て容易に放出されないものが望ましく、特にサイクロデ
キストリンは本発明において優れた効果を示す。The essence of the present invention is to combine the deodorant with polyurethane in the form of a clathrate as a guest compound, but the host compound, which is one of the components forming the clathrate, can also be used as appropriate in the form of a known clathrate-forming compound. selected from host compounds. Specific examples include crystalline cellulose, cyclodextrin, silica microbeads, and acrylic balloons.Those having a pore size of μ and whose clathrated guest compound is not easily released by water or solvents are preferable, and cyclodextrin in particular has an excellent effect in the present invention. shows.
また包接物の製造も従来知られた適宜の方法を応用でき
る。通常は飽和水溶液法もしくは混練法からの混合包接
された混合物を凍結乾燥、通風乾燥、噴霧乾燥或は、減
圧乾燥法で乾燥、粉砕して粉末状の包接物を得ることが
できる。Further, suitable methods known in the art can be applied to manufacture the clathrate. Usually, the mixed inclusion mixture obtained by the saturated aqueous solution method or the kneading method is dried by freeze drying, ventilation drying, spray drying, or reduced pressure drying, and then pulverized to obtain a powdery inclusion product.
この形状は、球状粉、粒状粉、樹技状粉、片状粉、角状
粉、海綿状粉、不規則形状粉等がある。This shape includes spherical powder, granular powder, dendritic powder, flaky powder, angular powder, spongy powder, irregularly shaped powder, etc.
使用に当たっては、いずれの形状のものでもよいが、そ
の大きさを定義するためここでは球状粉を代表させて示
すことにし5〜150μ径のものが好適である。In use, it may be of any shape, but in order to define its size, a spherical powder is shown here as a representative, and a powder having a diameter of 5 to 150 μm is suitable.
かくして得た包接物を皮膜形成性ポリウレタン溶液に分
散させる。ポリウレタンとしては適宜公知のポリウレタ
ンが用いられる。ポリウレタンの塗布とその後の発泡処
理も適宜公知の発泡ポリウレタン標識形成条件を採用し
得る。発泡処理は乾式法及び湿式法のいずれも採用し得
るが、特に湿式法が好ましい。この湿式法ではポリウレ
タンの有機溶媒溶液からなろ粘稠液に上記包接物を添加
混練して後、これを支持体に塗布し次いでこれを水等の
凝固浴に通すことにより樹脂化と発泡が行われる。なお
乾式法においても樹脂化と発泡の経過は類似している。The clathrate thus obtained is dispersed in a film-forming polyurethane solution. As the polyurethane, any known polyurethane can be used as appropriate. For the application of polyurethane and the subsequent foaming treatment, known foamed polyurethane label forming conditions may be adopted as appropriate. For the foaming treatment, either a dry method or a wet method can be employed, but the wet method is particularly preferred. In this wet method, the above-mentioned clathrates are added and kneaded into a Naro viscous liquid made from an organic solvent solution of polyurethane, and then this is applied to a support and then passed through a coagulation bath of water etc. to achieve resin formation and foaming. It will be done. In addition, the process of resin formation and foaming is similar in the dry method as well.
かかる樹脂化、発泡過程でガスが包接物と粘稠液の界面
を通って脱出し、その結果、包接物とポリウレタンとの
間に界面分離が起こり、発泡によって生じた多孔質ポリ
ウレタンの孔内にポリウレタンと一部が接着し且つ一部
が線孔を通して外部に通じている態様で包接物を組み込
んだ皮膜が形成される。尚、ポリウレタン溶1夜に包接
物と共にこれと同形状の不溶性固体を適宜量加えると、
これが空間形成補助剤として作用し、好ましい場合があ
る。ここに不溶性固体としては、酸化チタン、酸化珪素
等の無機質粒、銅、アルミニウム等の金属粒並びにその
フィラー、フッ素、ポリスチレン樹脂等の有機高分子化
合物粒並びにそのフィラー等をあげることができる。多
孔質ポリウレタンの細孔の大きさは5〜250μの範囲
にあることが好ましい。During the resin formation and foaming process, gas escapes through the interface between the clathrate and the viscous liquid, resulting in interfacial separation between the clathrate and the polyurethane, and the pores of the porous polyurethane created by foaming. A film is formed in which the clathrate is incorporated in such a manner that a portion thereof is adhered to the polyurethane and a portion thereof is communicated to the outside through the wire hole. In addition, if an appropriate amount of an insoluble solid having the same shape as the clathrate is added to the polyurethane solution overnight,
This acts as a space formation aid and may be preferable. Examples of the insoluble solid include inorganic particles such as titanium oxide and silicon oxide, metal particles such as copper and aluminum, and their fillers, and organic polymer compound particles such as fluorine and polystyrene resin, and their fillers. The pore size of the porous polyurethane is preferably in the range of 5 to 250 microns.
本発明において、支持体としては、洗濯、ドライクリー
ニング等に耐え得るものであれば消臭体の使用目的等に
応じて適宜のものを選択できる。In the present invention, any suitable support can be selected depending on the intended use of the deodorizer as long as it can withstand washing, dry cleaning, etc.
具体例としては、フィルム、シート、紙、不織布、マッ
ト、フオーム、プラスチック、成型品、木材、織物、編
物等があるが、通常のm維製品、プラスチック製品が好
ましく、これらの中でも繊維製品が好ましい。Specific examples include films, sheets, paper, nonwoven fabrics, mats, foams, plastics, molded products, wood, woven fabrics, knitted fabrics, etc., but ordinary textile products and plastic products are preferred, and among these, textile products are preferred. .
支持体へのポリウレタン溶液の塗布方法は、コーティン
グ、パッディング、スプレー、含浸等通常の方法が採用
される。表面のみに塗布しても、また肉厚の不織布等を
用いて内部にまで含浸させてもよい。Conventional methods such as coating, padding, spraying, and impregnation can be used to apply the polyurethane solution to the support. It may be applied only to the surface, or it may be impregnated into the inside using a thick non-woven fabric or the like.
本発明の消臭体における各成分の割合は広範囲に変化さ
せ得るが、通常消臭剤対包接用ホスト化合物が重量比で
01: 1〜15: 1で包接物対ポリウレタンが重量
比で0.01: 1〜0.2: 1の範囲が好まし
い。The proportions of each component in the deodorizer of the present invention can vary over a wide range, but typically the weight ratio of deodorant to clathrate host compound is 01:1 to 15:1 and the weight ratio of clathrate to polyurethane is 01:1 to 15:1. The range of 0.01:1 to 0.2:1 is preferred.
第1図に本発明消臭体の断面図を示す。FIG. 1 shows a sectional view of the deodorizing body of the present invention.
1の球状のものは微多孔質体に消臭剤を包接した包接体
粒子であり、2の皮膜状のものは、ポリウレタン樹脂の
皮膜層である。また皮膜周囲の空間部は該樹脂多孔質体
の連通空孔3を示し、4は支持体となる基材を示す。消
臭剤包接物がポリウレタン皮膜内外にランダムに分布固
定されているので消臭剤は外気と接触しやすい状態にあ
る。The spherical particles 1 are clathrate particles in which a deodorant is included in a microporous material, and the film-shaped particles 2 are a polyurethane resin film layer. Further, the space around the film indicates the communicating pores 3 of the porous resin body, and 4 indicates the base material serving as the support. Since the deodorant clathrates are randomly distributed and fixed inside and outside the polyurethane film, the deodorant is in a state where it easily comes into contact with the outside air.
本発明の消臭体は、その使用目的に応じて切断して粒状
、リボン状等好みの形態になし得る一方、サンドイッチ
状にラミネートして使用できる外、他の材料間に挾んで
使用することもできる。The deodorizing body of the present invention can be cut into a desired shape such as granules or ribbons depending on the purpose of use, and can also be used by laminating it in a sandwich or sandwiching it between other materials. You can also do it.
木発明の消臭体は、前記した特定構造に由来し、用いた
消臭剤の有する速効性を損なうことなく長期間安定にそ
の効果が持続すると共に耐洗濯性に濠れている。この耐
洗濯性は、洗浄処F!(洗濯、ドライクリーニング)に
より消臭効力を再生するという効果をも伴うのであや、
繰返しの洗浄処理によりより長期間の効果の持続を可能
とする。The deodorizing body of the Moki Invention is derived from the above-mentioned specific structure, and its effect is maintained stably for a long period of time without impairing the quick-acting properties of the deodorant used, and it has excellent washing resistance. This washing resistance is achieved by washing machine F! (washing, dry cleaning) also has the effect of regenerating the deodorizing effect.
Repeated cleaning treatments can maintain the effect for a longer period of time.
なお、本発明の消臭効果の確認は、代表的な悪臭ガスで
あるアンモニアガス(アルカリ性)と、硫化水素ガス(
r!a性)についてチェックした。臭いの測定は官能試
験法として直接表示法、空気稀釈法、また化学成分測定
法としてガスクロマトグラフ法、検知管法、比色法があ
るが、木発明で(よ北用式検知管を使用してチェックし
た。即ち500II11密閉容器中にアンモニアガス又
は硫化水素ガスを一定濃度注入し、同時に8 X 20
cmの消臭体を入れ、経済的にガス検知管で残留ガス
濃度を測定し消臭効果をチェックした。ガス検知管tよ
北沢産業■製ガスチックアンモニア用3LS硫化水素用
ALLを使用した。The deodorizing effect of the present invention was confirmed using ammonia gas (alkaline), which is a typical malodorous gas, and hydrogen sulfide gas (
r! A) was checked. Sensory testing methods for measuring odor include the direct display method and air dilution method, and methods for measuring chemical components include gas chromatography, detector tube methods, and colorimetric methods. That is, a fixed concentration of ammonia gas or hydrogen sulfide gas was injected into a 500 II 11 sealed container, and at the same time 8
cm of deodorizer was put in the container, and the residual gas concentration was economically measured using a gas detection tube to check the deodorizing effect. Gas detection tube 3LS for gastic ammonia and ALL for hydrogen sulfide manufactured by Kitazawa Sangyo ■ was used.
洗濯はJIS L217−103法に準じ、10回く
り返し実施し、またドライクリーニングは、JIS
L−1018E法に準じ、10回くり返し実施した。Washing was carried out 10 times according to JIS L217-103 method, and dry cleaning was carried out according to JIS L217-103 method.
The test was repeated 10 times according to the L-1018E method.
次に本発明の方法を実施例に基づいて説明する。Next, the method of the present invention will be explained based on examples.
これらは好ましい実施例の一つであるが本発明の製造方
法は例示の方法のみに限定されるものではない。Although these are one of the preferred embodiments, the manufacturing method of the present invention is not limited to only the illustrative method.
実施例 1
セルダールNΔ(祥光化学製消臭剤)とセルデックスN
(日本食品化工製ホスト化合物)を1=1の割合で混練
した後、減圧乾燥し消臭剤の包接物を得た。次にとの包
接物8重量部にジメチルホルムアミド40重量部を加え
十分に攪拌し、更にクリスボン8116 (大日本イ
ンキ工業製ウレタン樹脂)100重量部を加え30分間
攪拌し、混和溶液を得た。次にポリエステル不織布(1
00g/rn”)の片面にこの溶液をリバースコーター
にて塗布量50 g / m” (樹脂固形分換算)に
なるように塗布した後直ちに水中にて5分間凝固させ、
更に60℃の温湯にて10分間浸漬処理した後マングル
にて脱水し、120℃で5分間乾燥し、ポリエステル不
織布を支持体とする消臭体を得た。Example 1 Seldal NΔ (deodorant made by Shoko Chemical) and Seldex N
(Host compound manufactured by Nihon Shokuhin Kako) were kneaded in a ratio of 1=1 and then dried under reduced pressure to obtain a deodorant clathrate. Next, 40 parts by weight of dimethylformamide was added to 8 parts by weight of the clathrate and thoroughly stirred, and further 100 parts by weight of Crysbon 8116 (urethane resin manufactured by Dainippon Ink Industries) was added and stirred for 30 minutes to obtain a mixed solution. . Next, polyester nonwoven fabric (1
00g/rn") using a reverse coater to a coating amount of 50 g/m" (in terms of resin solid content), and immediately coagulated in water for 5 minutes.
The product was further immersed in hot water at 60°C for 10 minutes, dehydrated using a mangle, and dried at 120°C for 5 minutes to obtain a deodorizing body using a polyester nonwoven fabric as a support.
比較例 1
実施例1で使用した不慮布をセルダールNA(祥光化学
製消臭剤)の20%水溶液に浸漬後、絞り率120%に
なるようにマングルにて絞や、120℃で5分間乾燥し
消臭体を得た。Comparative Example 1 The random cloth used in Example 1 was dipped in a 20% aqueous solution of Cerdal NA (deodorizing agent made by Shoko Chemical), then squeezed with a mangle to a squeezing rate of 120%, and dried at 120°C for 5 minutes. A deodorizing body was obtained.
比較例 2
実施例1で得られた消臭剤を包接した微小多孔質包接物
10重量部にトルエン20重量部、クリスコートP10
19 (大日本インキ工業製アクリル樹脂)100重
呈部、クリスボンNX(大日本インキ工業製イソシアネ
ート架橋剤)1.5重量部を加え30分間攪拌し混和溶
液を得た。次に実施例1で使用した不織布の片面にリバ
ースコーターにて塗布量50 g / m (樹脂固形
分換算)になるように塗布した後150℃で30分間乾
燥し消臭体゛を得た。Comparative Example 2 10 parts by weight of the microporous clathrate containing the deodorant obtained in Example 1, 20 parts by weight of toluene, and Criscort P10
19 (acrylic resin manufactured by Dainippon Ink Industries) and 1.5 parts by weight of Crysbon NX (isocyanate crosslinking agent manufactured by Dainippon Ink Industries) were added and stirred for 30 minutes to obtain a mixed solution. Next, it was coated on one side of the nonwoven fabric used in Example 1 using a reverse coater to a coating amount of 50 g/m (in terms of resin solid content), and dried at 150°C for 30 minutes to obtain a deodorizing body.
以上の実施例及び比較例で得られ、た消臭体を使用し、
アンモニアガス、硫化水素ガスに対する消臭効果を測定
した。表1及び表2にその結果を示す。Using the deodorizer obtained in the above examples and comparative examples,
The deodorizing effect on ammonia gas and hydrogen sulfide gas was measured. The results are shown in Tables 1 and 2.
表1 (対アンモニアガス)
表2 (対硫化水素ガス)
実施例 2
アサヒガードAG−710(旭硝子製フッ素系撥水剤)
5%水溶液で撥水処理したナイロンタフタ(70d /
24 f 、 厖210本×緯90本)を゛実施例1
と同様の方法にて処理し消臭体を得た。Table 1 (Ammonia gas) Table 2 (Hydrogen sulfide gas) Example 2 Asahi Guard AG-710 (Asahi Glass fluorine water repellent)
Nylon taffeta (70d/
Example 1
A deodorizing body was obtained by processing in the same manner as above.
次に75μのポリエステルフィルム(東し製)にクリス
ボン4070 (大日本インキ工業製ウレタン樹脂)1
00重量部にトルエン30重量部を加えた混合溶液をリ
バースロールコータ−にて塗布量40 g/m′(1!
(脂固形分換算)になるように塗布し150℃で3分間
乾燥した。Next, 75μ polyester film (manufactured by Toshi) was coated with 1 part of Crisbon 4070 (urethane resin manufactured by Dainippon Ink Industries).
A mixed solution of 00 parts by weight and 30 parts by weight of toluene was coated with a reverse roll coater at a coating amount of 40 g/m' (1!
(based on fat solid content) and dried at 150°C for 3 minutes.
次に上記で得られた消臭体の多孔質皮膜面とポリエステ
ルフィルムの樹脂コート面を表面温度が130℃の熱ロ
ールとゴムロールからなる熱ロール間に通すことにより
貼り合わせ処理を行った後ナイロンタフタを剥離するこ
とによりポリエステルフィルムを支持体とする消臭体を
得た。Next, the porous film surface of the deodorizing body obtained above and the resin coated surface of the polyester film were bonded together by passing them between a heat roll with a surface temperature of 130°C and a rubber roll, and then the nylon film was bonded. By peeling off the taffeta, a deodorizing body having a polyester film as a support was obtained.
得られた消臭体を使用し、アンモニアガス、硫化水素ガ
スに対する消臭効果を測定した。表3及び表4にその結
果を示す。Using the obtained deodorizer, the deodorizing effect on ammonia gas and hydrogen sulfide gas was measured. Tables 3 and 4 show the results.
表3(対アンモニアガス)
表4 (7)硫化水素ガス)
実施例 3
スーパークリーンKS−YM−0(ココノエ製消臭剤)
とシリカマイクロビーズ(触媒化成工業製ホスト化合物
)を1: 1の割合で混練した後減圧乾燥し、消臭剤の
包接物を得た。次にこの包接物の6重量部にシラサギA
M−50(式日薬品工業製活性炭)6重it部及びジメ
チルホルムアミド40重量部を加え、更にクリスボン8
116 (大日本インキ工業製ポリウレタン樹II′f
J)100重1部を加え30分間攪拌し、混和溶液を得
た。Table 3 (Ammonia gas) Table 4 (7) Hydrogen sulfide gas) Example 3 Super Clean KS-YM-0 (Deodorant made by Coconoe)
and silica microbeads (host compound manufactured by Catalysts & Chemical Industry Co., Ltd.) in a ratio of 1:1 and dried under reduced pressure to obtain a deodorant clathrate. Next, add 6 parts by weight of this clathrate to White Heron A.
Add 6 parts of M-50 (activated carbon manufactured by Shikinichi Yakuhin Kogyo) and 40 parts by weight of dimethylformamide, and further add 8 parts of Crysbon.
116 (Polyurethane tree II'f manufactured by Dainippon Ink Industries)
J) 1 part by weight of 100 weight was added and stirred for 30 minutes to obtain a mixed solution.
次にナイロン不織布(75g/rn’)の片面にこの溶
液をリバースロールコータにて塗布量45g/rn″(
樹脂固形分換算)になるように塗布した後直ちに水中に
て5分間凝固させ、更に60℃の温湯にて10分間浸漬
処理した後マングルにて脱水し、120℃で5分間乾燥
しナイロン不織布を支持体とする消臭体を得た。得られ
た消臭体を使用し、アンモニアガス、硫化水素ガスに対
する消臭効果を測定した。表5及び表6にその結果を示
す。Next, apply this solution to one side of a nylon nonwoven fabric (75 g/rn') using a reverse roll coater in an amount of 45 g/rn'' (
Immediately after applying the resin to a solid content (based on resin solid content), it was coagulated in water for 5 minutes, further immersed in hot water at 60°C for 10 minutes, dehydrated in a mangle, and dried at 120°C for 5 minutes to form a nylon nonwoven fabric. A deodorizing body to be used as a support was obtained. Using the obtained deodorizer, the deodorizing effect on ammonia gas and hydrogen sulfide gas was measured. Tables 5 and 6 show the results.
表5(対アンモニアガス) 表6 (対硫化水素ガス)Table 5 (vs. ammonia gas) Table 6 (vs. hydrogen sulfide gas)
第1図は、本発明による消臭体の構成を示す概略拡大断
面図である。
1・・・・・・包接体粒子、 2・・・・・・皮膜層、
3・・・・・・連通空孔、 4・・・・・・基材、
5・・・・・・多孔質皮膜層、6・・・・・・支持体層
。
特許出願人 セー し ン株式会社 、代理人
弁理士 斉藤武彦゛、・′FIG. 1 is a schematic enlarged sectional view showing the structure of a deodorizing body according to the present invention. 1... Inclusion body particles, 2... Film layer,
3...Communicating pores, 4...Base material,
5... Porous film layer, 6... Support layer. Patent Applicant: SEEN Co., Ltd., Agent
Patent attorney Takehiko Saito゛、・′
Claims (1)
リウレタン多孔質皮膜を支持体上に設けてなる消臭体。 2、支持体が繊維からなる特許請求の範囲第1項記載の
消臭体。 3、ゲストが消臭剤である包接物を粉末状でポリウレタ
ン溶液に混入分散しこれを支持体に塗布して後、発泡処
理して多孔質皮膜層を形成させることを特徴とする消臭
体の製造法。[Scope of Claims] 1. A deodorizing body comprising a polyurethane porous film disposed on a support, in which a clathrate whose guest is a deodorant is dispersed and supported. 2. The deodorant according to claim 1, wherein the support is made of fiber. 3. A deodorizer characterized by mixing and dispersing a clathrate in which the guest is a deodorant in a polyurethane solution in powder form, applying this to a support, and then foaming it to form a porous film layer. How the body is manufactured.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61142845A JPH0687889B2 (en) | 1986-06-20 | 1986-06-20 | Washing-resistant deodorant and its manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61142845A JPH0687889B2 (en) | 1986-06-20 | 1986-06-20 | Washing-resistant deodorant and its manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62299266A true JPS62299266A (en) | 1987-12-26 |
JPH0687889B2 JPH0687889B2 (en) | 1994-11-09 |
Family
ID=15324949
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61142845A Expired - Fee Related JPH0687889B2 (en) | 1986-06-20 | 1986-06-20 | Washing-resistant deodorant and its manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0687889B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003038628A (en) * | 2001-07-26 | 2003-02-12 | Takahito Nakamura | Foamed deodorizing material and metal mold for foamed deodorizing material and method for manufacturing foamed deodorizing material using this metal mold |
JP2014008162A (en) * | 2012-06-28 | 2014-01-20 | Suminoe Textile Co Ltd | Filter for removing toilet odor |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58122022A (en) * | 1982-01-14 | 1983-07-20 | Shin Nisso Kako Co Ltd | Body and implement for absorbing harmful gas |
JPS61245840A (en) * | 1985-04-23 | 1986-11-01 | Konpetsukusu:Kk | Multi-element porous mineral foam deodorant and its preparation |
JPS61247462A (en) * | 1985-04-24 | 1986-11-04 | 松下電工株式会社 | Filter for air purifier |
-
1986
- 1986-06-20 JP JP61142845A patent/JPH0687889B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58122022A (en) * | 1982-01-14 | 1983-07-20 | Shin Nisso Kako Co Ltd | Body and implement for absorbing harmful gas |
JPS61245840A (en) * | 1985-04-23 | 1986-11-01 | Konpetsukusu:Kk | Multi-element porous mineral foam deodorant and its preparation |
JPS61247462A (en) * | 1985-04-24 | 1986-11-04 | 松下電工株式会社 | Filter for air purifier |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003038628A (en) * | 2001-07-26 | 2003-02-12 | Takahito Nakamura | Foamed deodorizing material and metal mold for foamed deodorizing material and method for manufacturing foamed deodorizing material using this metal mold |
JP2014008162A (en) * | 2012-06-28 | 2014-01-20 | Suminoe Textile Co Ltd | Filter for removing toilet odor |
Also Published As
Publication number | Publication date |
---|---|
JPH0687889B2 (en) | 1994-11-09 |
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