JPH0999048A - Liquid absorbent core material for thermal transpiration of aromatic - Google Patents
Liquid absorbent core material for thermal transpiration of aromaticInfo
- Publication number
- JPH0999048A JPH0999048A JP8202013A JP20201396A JPH0999048A JP H0999048 A JPH0999048 A JP H0999048A JP 8202013 A JP8202013 A JP 8202013A JP 20201396 A JP20201396 A JP 20201396A JP H0999048 A JPH0999048 A JP H0999048A
- Authority
- JP
- Japan
- Prior art keywords
- core material
- absorbent core
- fragrance
- aromatic
- liquid absorbent
- 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.)
- Pending
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 46
- 239000011162 core material Substances 0.000 title claims abstract description 38
- 230000002745 absorbent Effects 0.000 title claims abstract description 27
- 239000002250 absorbent Substances 0.000 title claims abstract description 27
- 125000003118 aryl group Chemical group 0.000 title abstract description 17
- 230000005068 transpiration Effects 0.000 title abstract description 12
- 238000010438 heat treatment Methods 0.000 claims abstract description 33
- 239000000835 fiber Substances 0.000 claims abstract description 12
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 8
- 239000000057 synthetic resin Substances 0.000 claims abstract description 8
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 5
- 239000003205 fragrance Substances 0.000 claims description 55
- 238000001704 evaporation Methods 0.000 claims description 24
- 230000008020 evaporation Effects 0.000 claims description 21
- 238000000465 moulding Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 abstract description 18
- 229920000877 Melamine resin Polymers 0.000 abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract description 3
- 239000002304 perfume Substances 0.000 abstract description 2
- 239000002386 air freshener Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000002093 peripheral effect Effects 0.000 description 6
- 230000008016 vaporization Effects 0.000 description 6
- 239000003814 drug Substances 0.000 description 5
- 239000002917 insecticide Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- -1 mercapto Benzimidazole-dilauryl-thio-di-propionate-2,2'-methylene-bis- (6-t-butyl-4-methylphenol) Chemical compound 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- GVJHHUAWPYXKBD-IEOSBIPESA-N (R)-alpha-Tocopherol Natural products OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 1
- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 1
- VOXXWSYKYCBWHO-UHFFFAOYSA-N 3-phenyllactic acid Chemical compound OC(=O)C(O)CC1=CC=CC=C1 VOXXWSYKYCBWHO-UHFFFAOYSA-N 0.000 description 1
- MRBKEAMVRSLQPH-UHFFFAOYSA-N 3-tert-butyl-4-hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1 MRBKEAMVRSLQPH-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- 235000005976 Citrus sinensis Nutrition 0.000 description 1
- 240000002319 Citrus sinensis Species 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-araboascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000402754 Erythranthe moschata Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229940087168 alpha tocopherol Drugs 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 239000004318 erythorbic acid Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- AOBORMOPSGHCAX-DGHZZKTQSA-N tocofersolan Chemical compound OCCOC(=O)CCC(=O)OC1=C(C)C(C)=C2O[C@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C AOBORMOPSGHCAX-DGHZZKTQSA-N 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、芳香剤加熱蒸散用
吸液芯材の改良に関し、さらに詳しくは、長期間安定し
た香質及び蒸散量が維持可能な芳香剤加熱蒸散用吸液芯
材に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improvement in a liquid absorbent core material for heating and fragrance heating, and more particularly, to a liquid absorbent core material for air freshener heating and evaporation capable of maintaining a stable fragrance and evaporation amount for a long period of time. It is about.
【0002】[0002]
【従来の技術】従来、芳香剤を含め薬剤を常温で揮散さ
せるための吸い上げ芯材としては、特開平2-200135号公
報に開示されているように、単糸太さが5 乃至20デニー
ルのアクリル樹脂繊維から成るスライバーを、メラミン
樹脂によって接着、成形され、その気孔率が40%乃至60
%とした非加熱型揮散用吸い上げ芯材が使用されてい
た。2. Description of the Related Art Conventionally, as a suction core material for volatilizing a drug including an aromatic agent at room temperature, as disclosed in JP-A-2-200135, a single yarn thickness of 5 to 20 denier is used. A sliver made of acrylic resin fiber is bonded and molded with melamine resin, and its porosity is 40% to 60%.
A non-heating type wicking core material for volatilization was used.
【0003】前述した従来の芳香剤非加熱型揮散用吸い
上げ芯材は、芳香剤薬液中に浸漬されたその下方端部か
ら毛細管現象により前記薬液をその上方端部に吸い上げ
て周辺に揮散させる作用をもたらすものであるが、該薬
液は芳香剤に水を混合させるために、高分子の活性剤が
必要になり、気孔率が低いと目詰まりの原因となる。一
方、非加熱条件下で芳香剤薬液を良く吸い上げ、十分に
揮散させるためにはその気孔率が40%乃至60%とするこ
とが必要とされている。前記芳香剤非加熱型揮散用吸い
上げ芯材の気孔率を40%以下とすると、非加熱状態下で
は必然的に芳香剤薬液の吸い上げ量が減少して、芳香効
果そのものが低下してしまう欠点があった。The above-mentioned conventional non-heated fragrance wicking core material for volatilization absorbs the chemical solution from its lower end, which is immersed in the fragrance chemical solution, to its upper end by capillary action and volatilizes it to the periphery. However, since the chemical solution requires a high-molecular activator in order to mix water with the fragrance, it causes clogging when the porosity is low. On the other hand, the porosity is required to be 40% to 60% in order to suck up the fragrance liquid well under the non-heating condition and to sufficiently volatilize it. When the porosity of the wicking core material for non-heated fragrance for fragrance is 40% or less, the wicking amount of the fragrance liquid inevitably decreases in the non-heated state, and the fragrance effect itself deteriorates. there were.
【0004】一方、加熱型吸い上げ芯材としての殺虫剤
加熱蒸散用吸液芯材が、例えば、特開平4-308501号公報
に提案されている。この殺虫剤加熱蒸散用吸液芯材は、
単糸太さが約3 デニールのアクリル、ナイロン、エステ
ル、等の合成樹脂繊維から成るトップまたはスライバー
を、メラミン、フェノール、尿素、等の熱硬化性樹脂で
接着、成形され、その気孔率が12%乃至18%に設定され
ていた。On the other hand, a liquid absorbent core material for heating and vaporizing an insecticide as a heating type suction core material has been proposed in, for example, Japanese Patent Laid-Open No. 4-308501. This absorbent core material for heat vaporization of insecticide is
The top or sliver made of synthetic resin fiber such as acrylic, nylon, ester, etc. with a single yarn thickness of about 3 denier is bonded and molded with a thermosetting resin such as melamine, phenol, urea, etc., and its porosity is 12 % To 18%.
【0005】上述した殺虫剤加熱蒸散用吸液芯材を使用
する殺虫剤薬液は、例えば、市販殺虫剤原液を若干の香
料とともに略97%乃至99%の含有量のケロシンで希釈し
て成っているので、殺虫剤薬液中に浸漬された前記殺虫
剤加熱蒸散用吸液芯材の下方端部から毛細管現象により
その上方端部に吸い上げられた前記薬液は、前記上端部
近傍を包囲するように配設された加熱手段により約140
℃以下に加熱されると、適正な蒸散量及び持続時間を以
てその周辺に放散して殺虫効果を発揮させるものであっ
た。An insecticide drug solution using the above-mentioned absorbent core material for heating and evaporation of insecticide is, for example, a commercially available insecticide stock solution diluted with kerosene having a content of about 97% to 99% together with some fragrance. Therefore, the chemical liquid sucked up from the lower end of the pesticide heating evaporation liquid absorbent core material immersed in the pesticide chemical liquid to its upper end by capillary action, surrounds the vicinity of the upper end. About 140 due to the heating means provided
When heated to a temperature of ℃ or less, it was released to the periphery with an appropriate amount and duration of transpiration to exert an insecticidal effect.
【0006】[0006]
【発明が解決しようとする課題】芳香剤を連続的に周囲
に供給するには加熱蒸散する方法によることが好まし
く、そのためには芳香剤では特に香質及び香料強度の点
で品質の良いものが要求されて来た。しかしながら従来
の気孔率が12乃至18%の芯材では、この要求を満たすも
のが得られなかった。In order to continuously supply the fragrance to the surroundings, it is preferable to use a method of heating and evaporating. For that purpose, the fragrance is of good quality especially in terms of fragrance and fragrance strength. It has been requested. However, a conventional core material having a porosity of 12 to 18% has not been able to satisfy the requirement.
【0007】本発明は、前述した従来の芳香剤非加熱型
揮散用吸い上げ芯材及び加熱蒸散用吸液芯材の問題点を
解消し、長期間安定した香質、香料強度及び蒸散量が維
持可能な芳香剤加熱蒸散用吸液芯材を提供することを目
的とするものである。The present invention solves the above-mentioned problems of the conventional non-heated wicking wicking core for fragrance and liquid wicking core for heat evaporation, and maintains stable fragrance, perfume strength and transpiration amount for a long period of time. It is an object of the present invention to provide a liquid absorbent core material for heating and evaporating an aromatic agent.
【0008】[0008]
【課題を解決するための手段】本発明のかかる目的は、
合成樹脂繊維のトップまたはスライバーを熱可塑性樹脂
によって接着、成形した吸液芯材の気孔率を25%乃至35
%として成ることを特徴とする芳香剤加熱蒸散用吸液芯
材によって達成される。The object of the present invention is to:
A synthetic resin fiber top or sliver bonded and molded with a thermoplastic resin has a porosity of 25% to 35
%, Which is achieved by a liquid absorbent core material for fragrance heat evaporation.
【0009】[0009]
【発明の実施の形態】本発明の芳香剤加熱蒸散用吸液芯
材の一実施態様について、添付した図面を参照して詳述
する。図1は、本発明の芳香剤加熱蒸散用吸液芯材20を
その内部に装着した芳香剤蒸散容器1の縦断面図であ
る。前記芳香剤蒸散容器1は、上方開口部2と下方開口
部3を有して全体が略円筒状に形成されている。その円
筒形状の構成をさらに詳しく述べれば、外周壁4及び内
周壁5、6 を二重あるいは三重に折り返すように形成し、
さらにその内部空間を横断して仕切るように中段7が配
設されている。BEST MODE FOR CARRYING OUT THE INVENTION An embodiment of the liquid absorbent core material for heating and vaporizing an aromatic agent of the present invention will be described in detail with reference to the accompanying drawings. FIG. 1 is a vertical cross-sectional view of an aromatic substance evaporation container 1 in which a liquid absorbent core material 20 for heating and evaporation of aromatic substances of the present invention is mounted. The fragrance evaporation container 1 has an upper opening 2 and a lower opening 3 and is formed in a substantially cylindrical shape as a whole. More specifically describing the cylindrical configuration, the outer peripheral wall 4 and the inner peripheral walls 5 and 6 are formed so as to be folded back in double or triple,
Further, a middle stage 7 is arranged so as to partition the interior space.
【0010】前記中段7の中央貫通孔周辺に沿って形成
された取付け口8の内周壁には雌ねじが凹設され、前記
下方開口部3から挿入された芳香剤薬液容器9の上部出
口10の外周面に凸設した雄ねじが前記雌ねじと螺合し
て、前記芳香剤薬液容器9を前記中段7に吊持可能に構
成されている。なお、芳香剤約液容器9は、前述したね
じの螺合によらず、ワンタッチで圧入するスナップジョ
イント方式で吊持させても良い。A female screw is provided on the inner peripheral wall of the mounting port 8 formed along the periphery of the central through hole of the middle tier 7, and an internal thread is formed in the upper opening 10 of the fragrance liquid medicine container 9 inserted from the lower opening 3. A male screw projectingly provided on the outer peripheral surface is screwed with the female screw so that the fragrance liquid chemical container 9 can be suspended on the middle stage 7. The fragrance liquid container 9 may be suspended by a one-touch snap-joint method instead of screwing the screws.
【0011】さらに、前記中段7の上方空間にあって前
記上方開口部2の近傍を横断して閉止するようにリング
状の加熱手段11が配設され、該加熱手段11の中央部は、
前記芳香剤加熱蒸散用吸液芯材20の外径よりも若干大き
な内径を以て開口され、前記芳香剤加熱蒸散用吸液芯材
20の上方端部22が前記加熱手段11の開口部下面と略一致
するように位置決めされている。なお、前記芳香剤加熱
蒸散用吸液芯材20の下方端部21は、前記中段7に吊持さ
れた前記芳香剤薬液容器9に中に収納された芳香剤薬液
ARに十分に浸漬され、吸収した該薬液ARをその毛細管現
象により矢印Aの方向に沿って吸い上げる。Further, a ring-shaped heating means 11 is arranged in the upper space of the middle stage 7 so as to traverse and close the vicinity of the upper opening 2, and the central portion of the heating means 11 is
The liquid absorbent core for heating and evaporation of aromatic substances is opened with an inner diameter slightly larger than the outer diameter of the liquid absorbent core for heating and evaporation of aromatic substance 20.
The upper end 22 of 20 is positioned so as to substantially coincide with the lower surface of the opening of the heating means 11. The lower end portion 21 of the absorbent core material 20 for heating and evaporating the fragrance is the fragrance liquid stored in the fragrance liquid container 9 suspended in the middle stage 7.
The drug solution AR, which is sufficiently immersed in the AR, is sucked up in the direction of arrow A by its capillary action.
【0012】前記芳香剤加熱蒸散用吸液芯材20は、単糸
太さが1デニール乃至15デニール、好ましくは2乃至4
デニールのアクリル、ナイロン、エステル、等の合成樹
脂繊維から成るトップあるいはスライバーを、メラミ
ン、フッ素系樹脂、等の熱硬化性樹脂によって接着さ
れ、前記芳香剤薬液容器9の形状、寸法、あるいは要求
される蒸散速度にもよるが、通常、太さが3乃至7mm
で、長さが3乃至30mmの棒状に成形され、且つその気
孔率が25%乃至35%の範囲内に設定される。なお、前記
合成樹脂繊維は、アクリル樹脂繊維が望ましく、また、
前記気孔率は30%乃至33%の範囲が望ましい。The liquid absorbent core material 20 for heating and vaporizing the fragrance has a single yarn thickness of 1 denier to 15 denier, preferably 2 to 4
A top or sliver made of synthetic resin fiber such as denier acrylic, nylon, ester, etc. is adhered by a thermosetting resin such as melamine, fluororesin, etc., and the shape, size, or required of the fragrance liquid medicine container 9 is required. Depending on the evaporation rate, the thickness is usually 3 to 7 mm
Then, it is formed into a rod shape having a length of 3 to 30 mm, and its porosity is set within the range of 25% to 35%. The synthetic resin fiber is preferably acrylic resin fiber,
The porosity is preferably in the range of 30% to 33%.
【0013】前記芳香剤薬液ARは、香料として、アルコ
ール類、エーテル類、灯油系(パラフィン系)、等を単
独又は組み合わせた可溶化剤に溶解させて使用可能なも
のであれば特に制約はなく、じゃ香、霊猫香、等の動物
性香料、植物性香料、ピネン、リモネン、等の合成香
料、あるいはこれらを組合せた香料、が使用できる。The fragrance liquid AR is not particularly limited as long as it can be used as a fragrance by dissolving it in a solubilizer in which alcohols, ethers, kerosene (paraffinic), etc. are used alone or in combination. , Animal fragrances such as musk, linguistic cat incense, plant fragrances, synthetic fragrances such as pinene and limonene, or fragrances combining these can be used.
【0014】さらに、前記芳香剤薬液ARは、前記香料の
前記可溶化剤との配合割合を1乃至50重量%、好ましく
は3乃至15重量%とする。また、前記香料組成物には、
加熱蒸散性を改善、調整するため、次のような化合物を
添加しても良い。 ・3,5 −ジ−t−ブチル−4−ヒドロキシトルエン(以
下、BHT と称する) ・3−t−ブチル−4−ヒドロキシアニソール ・3,5 −ジ−t−ブチル−4−ヒドロキシアニソール ・メルカプトベンズイミダゾール ・ジラウリル−チオ−ジ−プロピオネート ・2,2 ′−メチレン−ビス−(6−t−ブチル−4−メ
チルフェノール) ・2,2 ′−メチレン−ビス−(6−t−ブチル−4−エ
チルフェノール) ・4,4 ′−メチレン−ビス−(2,6 −ジ−t−ブチルフ
ェノール) ・4,4 ′−ブチリデン−ビス−(6−t−ブチル−3−
メチルフェノール) ・4,4 ′−チオ−ビス−(6−t−ブチル−3−メチル
フェノール) ・1,1 −ビス−(4−ヒドロキシフェニル)シクロヘキ
サン1,3,5 −トリメチル−2,4,6 −トリス(3,5 −ジ−
t−ブチル−4−ヒドロキシベンジル)ベンゼン ・トリス(2−メチル−4−ヒドロキシ−5−t−ブチ
ルフェニル)ブタン ・テトラキス[メチレン(3,5 −ジ−t−ブチル−4−
ヒドロキシヒドロシンナメート)]メタン ・オクタデシル−3,5 −ジ−t−ブチル−4−ヒドロキ
シヒドロシンナメート ・フェニル−β−ナフチルアミン ・N,N ′−ジフェニル−p−フェニレンジアミン ・2,2,4 −トリメチル−1,3 −ジヒドロキノリンポリマ
ー ・6−エトキシ−2,2,4 −トリメチル−1,3 −ジヒドロ
キノリン ・2−t−ブチル−4−メトキシフェニール ・3−t−ブチル−4−メトキシフェノール ・2,6 −ジ−t−ブチル−4−エチルフェノール ・ステアリル−β−(3,5 −ジ−t−ブチル−4−ヒド
ロキシフェニル)プロピオネート ・α−トコフェロール ・アスコンビン酸 ・エリソルビン酸 上記化合物は、その1種を単独で用いても良く、又、2
種以上併用することもできる。その使用量は、本発明の
揮散調整剤を添加して調整される薬液中に0.05〜2.0 重
量%、好ましくは約0.1 〜1.0 重量%含有される量とす
るのが好ましい。なお、上記化合物は、吸液芯自体に含
浸せしめても良く、この場合、これらの化合物は、単独
でも、又、2種以上を組み合わせて混合使用することも
できる。その使用量としては、芯全量の0.02〜3 重量
%、好ましくは0.05〜1 重量%の割合で用いる。Further, the fragrance liquid AR has a mixing ratio of the fragrance with the solubilizer of 1 to 50% by weight, preferably 3 to 15% by weight. Further, the fragrance composition,
The following compounds may be added to improve or adjust the heat transpiration property. * 3,5-di-t-butyl-4-hydroxytoluene (hereinafter referred to as BHT) * 3-t-butyl-4-hydroxyanisole * 3,5-di-t-butyl-4-hydroxyanisole * mercapto Benzimidazole-dilauryl-thio-di-propionate-2,2'-methylene-bis- (6-t-butyl-4-methylphenol) -2,2'-methylene-bis- (6-t-butyl-4) -Ethylphenol) -4,4'-methylene-bis- (2,6-di-t-butylphenol) -4,4'-butylidene-bis- (6-t-butyl-3-)
Methylphenol) ・ 4,4'-thio-bis- (6-t-butyl-3-methylphenol) ・ 1,1-bis- (4-hydroxyphenyl) cyclohexane 1,3,5-trimethyl-2,4 , 6-tris (3,5-di-
t-butyl-4-hydroxybenzyl) benzene-tris (2-methyl-4-hydroxy-5-t-butylphenyl) butane-tetrakis [methylene (3,5-di-t-butyl-4-)
Hydroxyhydrocinnamate)] methane Octadecyl-3,5-di-t-butyl-4-hydroxyhydrocinnamate Phenyl-β-naphthylamine N, N'-diphenyl-p-phenylenediamine 2,2,4 -Trimethyl-1,3-dihydroquinoline polymer-6-ethoxy-2,2,4-trimethyl-1,3-dihydroquinoline-2-t-butyl-4-methoxyphenyl-3-t-butyl-4-methoxy Phenol, 2,6-di-t-butyl-4-ethylphenol, stearyl-β- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, α-tocopherol, ascombic acid, erythorbic acid May be used alone, or 2
More than one species may be used in combination. The amount used is preferably 0.05 to 2.0% by weight, preferably about 0.1 to 1.0% by weight, in the chemical liquid prepared by adding the volatilization regulator of the present invention. The liquid absorbing core itself may be impregnated with the above compounds, and in this case, these compounds may be used alone or in combination of two or more kinds. The amount used is 0.02 to 3% by weight, preferably 0.05 to 1% by weight, based on the total weight of the core.
【0015】以上のように形成される本発明の芳香剤加
熱蒸散用吸液芯材20は、前記芳香剤蒸散容器1の所定位
置に装着され、前記上方端部22の近傍を前記リング状加
熱手段11により規定温度(最高200 ℃)に加熱される
と、前記芳香剤薬液容器9から毛細管現象で矢印Aの方
向に吸い上げられた前記芳香剤薬液ARが、蒸散を促され
て前記上方開口部2から矢印Bの方向に向けて適正な蒸
散量で長時間安定して放散する。The liquid absorbent core material 20 for fragrance heating and evaporation of the present invention formed as described above is mounted at a predetermined position of the fragrance evaporation container 1, and the vicinity of the upper end portion 22 is heated by the ring-shaped heating. When heated to a specified temperature (up to 200 ° C.) by the means 11, the fragrance chemical liquid AR sucked up from the fragrance chemical liquid container 9 in the direction of arrow A by capillary action is promoted to evaporate and the upper opening From 2 to the direction of arrow B, it is stably emitted for a long time with an appropriate transpiration amount.
【0016】[0016]
【実施例】本発明の新規な効果を、次に記す実施例によ
り一層明確にする。 1.〔芳香剤加熱蒸散用吸液芯材試料の作成条件〕 (1)繊維材…… アクリル樹脂繊維 単糸太さ:3デニール スライバー状 (2)接着樹脂…… メラミン樹脂 (3)成形寸法…… 直径5mm,長さ65mm (4)気孔率 …… 4種類:ビュレットによる測定法に
より測定した 20% 25% 35% 40% 2.〔芳香剤薬液試料の作成条件〕 (1)香料 … ネーブルオレンジ: 5重量部 (2)可溶化剤… エタノール : 94.5重量部 (3)添加物 … BHT : 0.1 重量部 以上の条件で作成された4種類の気孔率に設定された各
芳香剤加熱蒸散用吸液芯材試料を、上記条件で作成した
芳香剤薬液試料を収納した図1に示したような芳香剤蒸
散容器の芳香剤薬液容器に装着し、リング状加熱手段を
144 時間、140℃に加熱して、香質及び香料強度につい
て官能検査により比較評価した。その結果は、下記表A
の通りであった。また、同芳香剤薬液の蒸散量につい
て、室温25℃、24時間連続通電加熱して比較評価した。
その結果は下記表Bの通りであった。EXAMPLES The novel effects of the present invention will be further clarified by the following examples. 1. [Preparation conditions for liquid absorbent core material sample for heating and evaporation of fragrances] (1) Fiber material …… Acrylic resin fiber Single yarn thickness: 3 denier sliver shape (2) Adhesive resin …… Melamine resin (3) Molding dimension …… Diameter 5 mm, length 65 mm (4) Porosity …… 4 types: 20% 25% 35% 40% measured by burette measurement method 2. [Conditions for preparation of fragrance liquid chemical sample] (1) Fragrance ... Navel orange: 5 parts by weight (2) Solubilizer ... Ethanol: 94.5 parts by weight (3) Additives ... BHT: 0.1 parts by weight The aromatic agent liquid container of the aromatic substance evaporation container as shown in FIG. 1 in which the liquid absorbent core material samples for heating and vaporizing each of the aromatic substances set to four types of porosity are stored in the aromatic liquid agent samples prepared under the above conditions. Attached to the ring-shaped heating means
The mixture was heated at 140 ° C. for 144 hours and comparatively evaluated by sensory test for fragrance and fragrance strength. The results are shown in Table A below.
It was as follows. In addition, the amount of transpiration of the fragrance liquid was compared and evaluated by continuously heating it at room temperature at 25 ° C for 24 hours.
The results are shown in Table B below.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】[0019]
【発明の効果】上記表1及び表2から明らかなように、
前記芳香剤加熱蒸散用吸液芯材20は、その気孔率が25%
乃至35%のものが芳香剤の香質、香料強度、及び蒸散量
に関して、長期間にわたりバラツキも少なく安定して良
好あるいは適正な結果を得られることが確認された。以
上、記述したように、本発明の芳香剤加熱蒸散用吸液芯
材20は、合成樹脂繊維のトップまたはスライバーを熱可
塑性樹脂によって接着、略棒状に成形した吸液芯材の気
孔率を25%乃至35%として成るので、加熱によりその蒸
散作用が促進されても、香料の変質が生じ難く、芳香剤
を長期間安定した香質、香料強度及び蒸散量で放散させ
ることが可能になった。As is clear from Tables 1 and 2 above,
The porosity of the liquid absorption core material 20 for heating and vaporizing the aromatic agent is 25%.
It was confirmed that about 35% to 35% of the fragrance, fragrance strength, and transpiration amount of the fragrance have little variation over a long period of time, and stable or good results can be obtained. As described above, the liquid absorbent core material 20 for fragrance heating and evaporation of the present invention has the porosity of the liquid absorbent core material formed by bonding a synthetic resin fiber top or sliver with a thermoplastic resin into a substantially rod shape. % To 35%, the fragrance does not easily change even if its transpiration action is promoted by heating, and it is possible to release the fragrance with a long-term stable fragrance, fragrance strength and transpiration amount. .
【図1】本発明の芳香剤加熱蒸散用吸液芯材を使用する
芳香剤蒸散容器の縦断面図である。FIG. 1 is a vertical cross-sectional view of an air freshener evaporation container using the liquid absorbent core material for air freshening of air freshener of the present invention.
1 芳香剤蒸散容器 2 上方開口部 3 下方開口部 4 外周壁 5.6 内周壁 7 中段 9 芳香剤薬液容器 11 リング状加熱手段 20 芳香剤加熱蒸散用吸液芯材 21 下方端部 22 上方端部 AR 芳香剤薬液 1 Air freshener evaporation container 2 Upper opening 3 Lower opening 4 Outer peripheral wall 5.6 Inner peripheral wall 7 Middle stage 9 Air freshener chemical liquid container 11 Ring-shaped heating means 20 Absorbent core material for air freshening and evaporation 21 Lower end 22 Upper end AR Air freshener
Claims (1)
を熱可塑性樹脂によって接着、成形した吸液芯材の気孔
率を25%乃至35%として成ることを特徴とする芳香剤加
熱蒸散用吸液芯材。1. A liquid absorbent core material for heating and evaporation of fragrances, characterized in that the liquid absorbent core material obtained by bonding and molding a synthetic resin fiber top or sliver with a thermoplastic resin has a porosity of 25% to 35%. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8202013A JPH0999048A (en) | 1995-08-01 | 1996-07-31 | Liquid absorbent core material for thermal transpiration of aromatic |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7-196635 | 1995-08-01 | ||
JP19663595 | 1995-08-01 | ||
JP8202013A JPH0999048A (en) | 1995-08-01 | 1996-07-31 | Liquid absorbent core material for thermal transpiration of aromatic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0999048A true JPH0999048A (en) | 1997-04-15 |
Family
ID=26509884
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8202013A Pending JPH0999048A (en) | 1995-08-01 | 1996-07-31 | Liquid absorbent core material for thermal transpiration of aromatic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0999048A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005137966A (en) * | 2003-11-04 | 2005-06-02 | Matsushita Electric Works Ltd | Electrostatic atomizer |
EP1415670A4 (en) * | 2001-08-03 | 2006-04-19 | St Chemical Co Ltd | Liquid-absorbing core |
JP2010243037A (en) * | 2009-04-03 | 2010-10-28 | Eiken Industries Co Ltd | Portable humidifier |
-
1996
- 1996-07-31 JP JP8202013A patent/JPH0999048A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1415670A4 (en) * | 2001-08-03 | 2006-04-19 | St Chemical Co Ltd | Liquid-absorbing core |
JP2005137966A (en) * | 2003-11-04 | 2005-06-02 | Matsushita Electric Works Ltd | Electrostatic atomizer |
JP2010243037A (en) * | 2009-04-03 | 2010-10-28 | Eiken Industries Co Ltd | Portable humidifier |
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