JP2000189789A - Moisture regulating material usable repeatedly and its production - Google Patents
Moisture regulating material usable repeatedly and its productionInfo
- Publication number
- JP2000189789A JP2000189789A JP11000612A JP61299A JP2000189789A JP 2000189789 A JP2000189789 A JP 2000189789A JP 11000612 A JP11000612 A JP 11000612A JP 61299 A JP61299 A JP 61299A JP 2000189789 A JP2000189789 A JP 2000189789A
- Authority
- JP
- Japan
- Prior art keywords
- hydroxide
- humidity
- water vapor
- metal hydroxide
- hygroscopic
- 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
Landscapes
- Building Environments (AREA)
- Drying Of Gases (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
【0001】[0001]
【本発明の属する技術分野】本発明は、耐久性に優れ、
省エネルギーや環境付加軽減の観点からも既存の結露防
止材料に優る結露防止材料等として有用な新規な調湿材
料及びその製造方法に関するものである。TECHNICAL FIELD [0001] The present invention is excellent in durability,
The present invention relates to a novel humidity control material useful as an anti-condensation material and the like, which is superior to existing anti-condensation materials, from the viewpoint of energy saving and reduction of environmental load, and a method for producing the same.
【0002】[0002]
【従来の技術】従来の日本の家屋では、木材や土壁等の
建築材料が用いられていた。これらの材料はそれ自身が
調湿性能を有しているが、建築方法自体も高温多湿時の
避暑を考慮した気密性の低いものであった。しかし、最
近の建築物は調湿性の劣る新建材が多用され、さらに高
断熱化・高気密化の促進により、内部結露の発生及びそ
れに伴う壁面の濡れやシミの発生、カビやダニなどの繁
殖などの問題が生じている。このような居住環境の改変
に伴い、結露防止のための技術の重要性は増すばかりで
ある。従来では、乾燥剤として生石灰(酸化カルシウ
ム)やシリカゲルなどを利用したり、除湿器、エアコン
等の空調設備を運転することにより、結露の発生を防い
でいた。2. Description of the Related Art In conventional Japanese houses, building materials such as wood and earth walls have been used. These materials themselves have humidity control performance, but the construction method itself has low airtightness in consideration of summer heat during high temperature and high humidity. However, in recent years, new construction materials with poor humidity control have been used extensively, and due to the promotion of high insulation and high airtightness, the occurrence of internal dew condensation, the resulting wetting of walls and generation of spots, and the propagation of mold and mites And other problems. With such a change in living environment, the importance of technology for preventing dew condensation is only increasing. Conventionally, dew condensation has been prevented by using quicklime (calcium oxide), silica gel, or the like as a desiccant, or by operating an air conditioner such as a dehumidifier or an air conditioner.
【0003】[0003]
【発明が解決しようとする課題】上述の乾燥剤はいずれ
も吸湿力が強く、除湿能力を制御しにくい。また、一度
飽和点に達すると吸湿機能が大幅に低下するため、吸湿
有効期間は短い。さらに、一度吸収した水分を分離し吸
湿機能を回復させることが容易ではないため、繰り返し
再利用することが困難である。一方、除湿器、エアコン
等の空調設備の運転による除湿は、エネルギーを消費す
る点及び経済性の点から好ましいものではない。All of the above desiccants have a strong hygroscopicity, and it is difficult to control the dehumidifying ability. Further, once the saturation point is reached, the moisture absorption function is greatly reduced, so that the moisture absorption effective period is short. Furthermore, since it is not easy to separate the once absorbed moisture and restore the moisture absorbing function, it is difficult to repeatedly reuse the moisture. On the other hand, dehumidification by operation of an air conditioner such as a dehumidifier and an air conditioner is not preferable in terms of energy consumption and economy.
【0004】従って、本発明の目的は、高湿度条件下に
おいて多量の水蒸気を吸収し、かつ通常の湿度条件下に
おいて吸着した水蒸気の大部分を容易に放出することが
でき、それによって繰り返し利用可能な結露防止材料等
として好適に用いることができる調湿材料、及びかかる
調湿材料を比較的簡単にかつ低コストで製造できる方法
を提供することにある。[0004] It is therefore an object of the present invention to absorb large amounts of water vapor under high humidity conditions and to easily release most of the adsorbed water vapor under normal humidity conditions, thereby making it possible to use repeatedly. It is an object of the present invention to provide a humidity control material that can be suitably used as an anti-condensation prevention material and the like, and a method of manufacturing such a humidity control material relatively easily and at low cost.
【0005】[0005]
【課題を解決するための手段】前記目的を達成するため
に、本発明によれば、金属塩化物水溶液の水素イオン濃
度をアンモニア水溶液で調整することにより金属水酸化
物を析出させ、さらに温水浴中にて攪拌することにより
得られる水酸化物ゲルを、吸湿性の副生成物を熱分解し
ない温度で熱処理することにより、多孔質金属水酸化物
と吸湿性の塩化アンモニウムの複合体を製造することを
特徴とする調湿材料の製造方法が提供される。さらに本
発明によれば、細孔半径10nm未満のメソポア細孔を
有する多孔質金属水酸化物と吸湿性物質の複合体であ
り、相対湿度80%以上の高湿度条件下において自重の
60%以上の水蒸気を吸収し、かつ相対湿度60%程度
以下の通常の湿度条件下において吸着した水蒸気の大部
分を容易に放出することができる繰り返し利用可能な調
湿材料が提供される。According to the present invention, a metal hydroxide is precipitated by adjusting the hydrogen ion concentration of an aqueous metal chloride solution with an aqueous ammonia solution. A composite of a porous metal hydroxide and a hygroscopic ammonium chloride is produced by heat-treating a hydroxide gel obtained by stirring in a solution at a temperature at which a hygroscopic by-product is not thermally decomposed. A method for producing a humidity control material is provided. Furthermore, according to the present invention, a composite of a porous metal hydroxide having mesopore pores having a pore radius of less than 10 nm and a hygroscopic substance, and 60% or more of its own weight under a high humidity condition of 80% or more in relative humidity. And a reusable humidity control material capable of easily releasing most of the adsorbed water vapor under normal humidity conditions of about 60% or less relative humidity.
【0006】[0006]
【発明の実施の形態】本発明の方法は、金属塩化物水溶
液から金属水酸化物を析出させる際に副生する吸湿性物
質を積極的に複合化するために、得られる水酸化物ゲル
を、吸湿性の副生成物を熱分解しない程度の温度で熱処
理することを特徴とするものである。その結果、本発明
によれば、多孔質金属水酸化物と吸湿性物質の複合体か
らなり、多孔質金属水酸化物の毛管凝縮現象と共存吸湿
性物質の吸湿性を併せて利用し、相対湿度80%以上の
湿度環境において空気中の水蒸気を吸収し、相対湿度6
0%程度以下の湿度環境において水蒸気を放出する優れ
た調湿機能を有する多孔質材料が提供される。BEST MODE FOR CARRYING OUT THE INVENTION The method of the present invention is intended to positively complex a hygroscopic substance by-produced when a metal hydroxide is precipitated from an aqueous metal chloride solution. And heat-treating at a temperature at which the hygroscopic by-product is not thermally decomposed. As a result, according to the present invention, a composite of a porous metal hydroxide and a hygroscopic substance is used, and the capillary condensation phenomenon of the porous metal hydroxide and the hygroscopic property of the coexisting hygroscopic substance are used together, Absorbs water vapor in the air in a humidity environment of 80% or more, and has a relative humidity of 6%.
A porous material having an excellent humidity control function of releasing water vapor in a humidity environment of about 0% or less is provided.
【0007】以下、本発明についてさらに詳細に説明す
る。本発明の方法で原料として用いる金属塩化物水溶液
としては塩化アルミニウム水溶液等があり、水素イオン
濃度を調整することで水酸化物として析出するものであ
ればよい。水素イオン濃度の調整剤は、錯イオン形成等
により水酸化物の析出を妨害するものでなければよい。
好ましくは、副生成物が熱処理時にも除去されることな
く、かつその副生成物が適度な吸湿性を有するものがよ
い。さらに具体的には、上記塩化物水溶液の場合、アン
モニア水溶液が好適なものとして例示される。この金属
塩化物水溶液に適当な水素イオン濃度の調整剤を添加し
て水酸化物が析出する水素イオン濃度に調整した後、適
宜の方法、例えば100℃未満の温水浴中で攪拌する等
の処理を行い、金属水酸化物が均一に分散したゲルを調
製する。このゲルを適宜な方法、例えば約100℃の恒
温槽内で乾燥させた後、所定の温度で適切な時間保持す
ることにより、脱水反応を起こさせて多孔質水酸化物化
させる。加熱条件としては、構造水の脱離だけが生じ、
吸湿性を有する副生成物が熱分解で除去されない温度以
下で加熱する。熱処理後、適宜な方法、例えば乳鉢等を
用いての機械的な解砕と篩い分け等により粒度を調整
し、多孔質材料を得る。Hereinafter, the present invention will be described in more detail. The aqueous metal chloride solution used as a raw material in the method of the present invention includes an aluminum chloride aqueous solution and the like, as long as it can precipitate as a hydroxide by adjusting the hydrogen ion concentration. The regulator of the hydrogen ion concentration need only be one that does not interfere with the precipitation of hydroxide due to complex ion formation or the like.
Preferably, the by-product is not removed during the heat treatment, and the by-product has an appropriate hygroscopicity. More specifically, in the case of the above chloride aqueous solution, an aqueous ammonia solution is exemplified as a preferable one. After adding an appropriate regulator of hydrogen ion concentration to the aqueous metal chloride solution to adjust the hydrogen ion concentration at which hydroxides are precipitated, an appropriate method such as stirring in a warm water bath of less than 100 ° C. To prepare a gel in which the metal hydroxide is uniformly dispersed. After drying this gel in an appropriate method, for example, in a thermostat at about 100 ° C., the gel is maintained at a predetermined temperature for an appropriate time to cause a dehydration reaction to form a porous hydroxide. As heating conditions, only desorption of structural water occurs,
The heating is performed at a temperature not higher than the temperature at which by-products having hygroscopicity are not removed by thermal decomposition. After the heat treatment, the particle size is adjusted by an appropriate method, for example, mechanical crushing using a mortar or the like and sieving to obtain a porous material.
【0008】[0008]
【実施例】以下、実施例及び比較例を示して本発明につ
いてより具体的に説明するが、本発明が下記実施例に限
定されるものでないことはもとよりである。EXAMPLES Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples, but it goes without saying that the present invention is not limited to the following Examples.
【0009】実施例 塩化アルミニウム0.1モルを蒸留水300mlに溶解
した後、25wt%アンモニア水41.4gを加え、ア
ルミニウムの水酸化物を析出させた。その後、90℃の
温水浴中で3時間処理して熟成させ、水酸化アルミニウ
ムをゲル化させた。ゲルを100℃の恒温槽内で一昼夜
保持して乾燥させた後、電気炉にて300℃で4時間保
持して熱処理し、試料を得た。熱処理温度を300℃と
した理由は、副生成物である塩化アンモニウムが338
℃で昇華してしまうためであり、水酸化アルミニウムが
脱水して多孔質化し、かつ副生成物である塩化アンモニ
ウムが昇華により消失しない温度であればよい。この試
料をアルミナ乳鉢にて解砕し、70メッシュの篩いを通
過したものを測定試料として、以下の測定に供した。EXAMPLE After dissolving 0.1 mol of aluminum chloride in 300 ml of distilled water, 41.4 g of 25 wt% aqueous ammonia was added to precipitate aluminum hydroxide. Thereafter, the mixture was aged in a warm water bath at 90 ° C. for 3 hours for aging to gel the aluminum hydroxide. The gel was kept in a thermostat at 100 ° C. for 24 hours, dried and then heat-treated at 300 ° C. for 4 hours in an electric furnace to obtain a sample. The reason for setting the heat treatment temperature to 300 ° C. is that ammonium chloride as a by-product
This is because sublimation occurs at a temperature of ° C., so long as the temperature is such that aluminum hydroxide is dehydrated to be porous and ammonium chloride as a by-product does not disappear by sublimation. This sample was crushed in an alumina mortar, and a sample passed through a 70-mesh sieve was used as a measurement sample for the following measurement.
【0010】得られた試料の同定は粉末X線回折測定に
より行った。細孔分布は窒素吸着法を用いて測定した。
また、吸・放湿特性は、吸着平衡自動測定装置を用い、
測定系内の温度を一定(25℃)にして、水蒸気圧を変
化させて平衡状態に達したときの試料重量の変化から吸
着量を求める方法(重量法)により測定した。水蒸気吸
着量は、絶乾状態の試料重量に対する吸着水重量の割合
を示す。実施例で得られた試料の粉末X線回折パターン
を図1に示す。回折パターンは、試料がγ−AlOOH
と塩化アンモニウムの複合物であることを示している。
また、実施例で得られた試料の細孔分布を図2に示す。
得られた試料の細孔分布は細孔半径約2nmにピークト
ップを示している。さらに、実施例で得られた試料の吸
・放湿特性(吸着等温線)を図3に示す。得られた試料
の吸着等温線は相対湿度約80%で急激に立ち上がり、
脱着等温線から相対湿度約60%において吸着していた
水蒸気の大部分を放湿していることがわかる。The obtained sample was identified by powder X-ray diffraction measurement. The pore distribution was measured using a nitrogen adsorption method.
The absorption and desorption characteristics are measured using an automatic adsorption equilibrium measurement device.
The temperature in the measurement system was kept constant (25 ° C.), and the measurement was performed by a method (gravimetric method) in which the amount of adsorption was determined from the change in the sample weight when the water vapor pressure was changed to reach an equilibrium state. The amount of water vapor adsorption indicates the ratio of the weight of adsorbed water to the weight of a sample in a completely dry state. FIG. 1 shows a powder X-ray diffraction pattern of the sample obtained in the example. The diffraction pattern shows that the sample is γ-AlOOH
And ammonium chloride.
FIG. 2 shows the pore distribution of the sample obtained in the example.
The pore distribution of the obtained sample shows a peak top at a pore radius of about 2 nm. FIG. 3 shows the absorption / desorption characteristics (adsorption isotherm) of the sample obtained in the example. The adsorption isotherm of the obtained sample rapidly rises at about 80% relative humidity,
It can be seen from the desorption isotherm that most of the adsorbed water vapor was released at a relative humidity of about 60%.
【0011】比較例 図4に従来より乾燥剤として用いられてきた、酸化カル
シウム及びシリカゲルの吸・放湿特性(吸着等温線)示
す。酸化カルシウムは、吸水後、水酸化カルシウムに変
化するため、乾燥による再利用は困難である。また、シ
リカゲルは相対湿度70%で飽和し、再利用する際には
相対湿度20%以下で乾燥させる必要がある。このよう
に、どちらも繰り返し利用する結露防止用途には不適当
である。Comparative Example FIG. 4 shows the absorption / desorption characteristics (adsorption isotherm) of calcium oxide and silica gel which have been conventionally used as a desiccant. Calcium oxide changes to calcium hydroxide after absorbing water, and is difficult to reuse by drying. Further, silica gel is saturated at a relative humidity of 70%, and must be dried at a relative humidity of 20% or less when reused. Thus, both are unsuitable for dew condensation prevention applications which are used repeatedly.
【0012】[0012]
【発明の効果】以上のように、本発明の方法によれば、
結露防止材料として有用な多孔質金属水酸化物と吸湿性
物質の複合体からなる調湿材料を、比較的簡単にかつ低
コストで製造できる。このような複合材料は、前記した
ような優れた水分吸着・脱着性能を有するため、極めて
良好な結露防止機能とそれの繰り返し利用が可能であ
り、また、湿度調整機能をも備えているため、結露防止
剤としての利用に止まらず、調湿材としても好適な材料
ある。As described above, according to the method of the present invention,
A humidity control material comprising a composite of a porous metal hydroxide and a hygroscopic substance useful as a dew condensation preventing material can be produced relatively easily and at low cost. Such a composite material has excellent moisture adsorption / desorption performance as described above, so that an extremely good dew condensation preventing function and its repeated use are possible, and also has a humidity adjusting function. It is not limited to use as an anti-condensation agent, but is also suitable as a humidity control material.
【図1】本発明の実施例で調製された材料の粉末X線回
折パターンを示すグラフである。FIG. 1 is a graph showing a powder X-ray diffraction pattern of a material prepared in an example of the present invention.
【図2】本発明の実施例で調製された材料の細孔分布を
示すグラフである。FIG. 2 is a graph showing a pore distribution of a material prepared in an example of the present invention.
【図3】本発明の実施例で調製された材料の水蒸気の吸
着・脱着等温線を示すグラフである。FIG. 3 is a graph showing water vapor adsorption / desorption isotherms of materials prepared in Examples of the present invention.
【図4】本発明の比較例で提示された従来からの吸湿材
料(乾燥剤)の水蒸気の吸着・脱着等温線を示すグラフ
である。FIG. 4 is a graph showing water vapor adsorption / desorption isotherms of a conventional moisture absorbing material (drying agent) presented in a comparative example of the present invention.
フロントページの続き (72)発明者 鈴木 正哉 岐阜県多治見市松坂町4−8−212 (72)発明者 大橋 文彦 愛知県名古屋市西区平出町169番地の2 サンドエル3C (72)発明者 犬飼 恵一 愛知県名古屋市中川区西伏屋1丁目605番 地 (72)発明者 渡村 信治 愛知県名古屋市千種区南ヶ丘1−7−12 (72)発明者 芝崎 靖雄 愛知県名古屋市熱田区大宝2−4 (72)発明者 福島 恭子 富山県黒部市天神新115 (72)発明者 相川 和夫 富山県滑川市上小泉526−2 Fターム(参考) 2E001 DB03 GA03 JA00 JB00 4D052 AA08 GA03 GA04 GB03 GB11 GB12 GB13 GB14 GB16 GB17 GB18 HA00 4G066 AA20B AA32A AA32B AA52D BA22 BA23 BA31 BA36 BA42 CA43 DA03 FA05 FA14 FA21 GA06 GA31 Continued on the front page (72) Inventor Masaya Suzuki 4-8-212, Matsuzaka-cho, Tajimi-shi, Gifu (72) Inventor Fumihiko Ohashi 169-2, Hirade-cho, Nishi-ku, Nagoya-shi, Aichi 2 Sandel 3C (72) Inventor Keiichi Inukai Aichi 1-605, Nishifushiya, Nakagawa-ku, Nagoya-shi, Japan (72) Inventor Shinji Watari 1-7-12 Minamigaoka, Chigusa-ku, Nagoya-shi, Aichi (72) Inventor Yasuo Shibasaki 2-Taobao, Atsuta-ku, Nagoya-shi, Aichi 4 (72) Inventor Kyoko Fukushima 115 Tenjin Shin, Kurobe City, Toyama Prefecture (72) Inventor Kazuo Aikawa 526-2 Kamikoizumi, Namerikawa City, Toyama F Term (Reference) 2E001 DB03 GA03 JA00 JB00 4D052 AA08 GA03 GA04 GB03 GB11 GB12 GB13 GB14 GB16 GB17 GB18 HA00 4G066 AA20B AA32A AA32B AA52D BA22 BA23 BA31 BA36 BA42 CA43 DA03 FA05 FA14 FA21 GA06 GA31
Claims (2)
ンモニア水溶液で調整することにより金属水酸化物を析
出させ、さらに温水浴中にて攪拌することにより得られ
る水酸化物ゲルを、吸湿性の副生成物を熱分解しない温
度で熱処理することにより、多孔質金属水酸化物と吸湿
性の塩化アンモニウムの複合体を製造することを特徴と
する調湿材料の製造方法。1. A metal hydroxide is precipitated by adjusting the hydrogen ion concentration of an aqueous metal chloride solution with an aqueous ammonia solution, and the hydroxide gel obtained by stirring in a warm water bath is converted into a hygroscopic gel. A method for producing a humidity control material, comprising producing a composite of a porous metal hydroxide and hygroscopic ammonium chloride by heat-treating a by-product at a temperature that does not cause thermal decomposition.
有する多孔質金属水酸化物と吸湿性物質の複合体であ
り、相対湿度80%以上の高湿度条件下において自重の
60%以上の水蒸気を吸収し、かつ相対湿度60%程度
以下の通常の湿度条件下において吸着した水蒸気の大部
分を容易に放出することができる繰り返し利用可能な調
湿材料。2. A composite of a porous metal hydroxide having mesopore pores having a pore radius of less than 10 nm and a hygroscopic substance, and having a relative humidity of 80% or more and a water vapor of 60% or more of its own weight under a high humidity condition of 80% or more. Reusable moisture control material that can absorb water and easily release most of the adsorbed water vapor under normal humidity conditions of about 60% or less relative humidity.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP00061299A JP3554752B2 (en) | 1999-01-05 | 1999-01-05 | Reusable humidity control material and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP00061299A JP3554752B2 (en) | 1999-01-05 | 1999-01-05 | Reusable humidity control material and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000189789A true JP2000189789A (en) | 2000-07-11 |
JP3554752B2 JP3554752B2 (en) | 2004-08-18 |
Family
ID=11478568
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP00061299A Expired - Lifetime JP3554752B2 (en) | 1999-01-05 | 1999-01-05 | Reusable humidity control material and method for producing the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3554752B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6765753B2 (en) | 2002-03-08 | 2004-07-20 | Kabushiki Kaisha Toshiba | Disk apparatus |
JPWO2018142758A1 (en) * | 2017-01-31 | 2019-11-21 | パナソニックIpマネジメント株式会社 | Electrolytic capacitor |
-
1999
- 1999-01-05 JP JP00061299A patent/JP3554752B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6765753B2 (en) | 2002-03-08 | 2004-07-20 | Kabushiki Kaisha Toshiba | Disk apparatus |
JPWO2018142758A1 (en) * | 2017-01-31 | 2019-11-21 | パナソニックIpマネジメント株式会社 | Electrolytic capacitor |
JP7223968B2 (en) | 2017-01-31 | 2023-02-17 | パナソニックIpマネジメント株式会社 | Electrolytic capacitor |
Also Published As
Publication number | Publication date |
---|---|
JP3554752B2 (en) | 2004-08-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5364455A (en) | Silica gels of controlled pore size as desiccant materials and processes for producing same | |
JP2006240956A (en) | Amorphous aluminum silicate, adsorbent having the same, dehumidifying rotor and air conditioner | |
JP6761999B2 (en) | A water vapor adsorbent in which a hygroscopic salt is supported on an amorphous aluminum silicate granule. | |
KR101641985B1 (en) | Honeycomb matrix comprising macroporous desiccant, process and use thereof | |
CN108144575B (en) | Graphite sulfide, silica gel and lithium chloride curing composite dehumidifying agent and preparation method thereof | |
JP5392121B2 (en) | Method for producing hygroscopic agent | |
JP3554752B2 (en) | Reusable humidity control material and method for producing the same | |
JP3869136B2 (en) | Manufacturing method of humidity control material | |
JP3089395B2 (en) | Porous material with autonomous humidity control function | |
JP3418122B2 (en) | Method for producing granular moisture absorbing and releasing material | |
JP3793809B2 (en) | Porous material comprising hollow fiber aluminum silicate and method for producing the same | |
JP2002052337A (en) | Air-conditioning material exhibiting excellent water absorption behavior at high-humidity | |
JP3871174B2 (en) | Method for producing humidity conditioning material having antibacterial function | |
RU2042695C1 (en) | Heat accumulating material and a method of its production | |
JP3786230B2 (en) | Manufacturing method of alumina humidity conditioning material | |
JP3360111B2 (en) | Moisture absorbing and releasing material with low hysteresis and durable water vapor | |
KR100427264B1 (en) | Powdery humidity self control material and its preparation method | |
JP4041884B2 (en) | Porous material showing water vapor adsorption / desorption behavior and use thereof | |
JP2005230797A (en) | Adsorbing agent comprising zeolite for heat pump and its production method and its use | |
SU1657219A1 (en) | Impregnated air drier and process for preparing same | |
JP3282238B2 (en) | Method for producing chemical activated carbon | |
JPH11137947A (en) | Dehumidifying air conditioner | |
JP3106112B2 (en) | Manufacturing method of drying and deodorizing agent. | |
JP7248989B2 (en) | Chemical heat storage material and its manufacturing method | |
JPH11165064A (en) | Dehumidifying air conditioner |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20031212 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20040316 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20040402 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20040402 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R154 | Certificate of patent or utility model (reissue) |
Free format text: JAPANESE INTERMEDIATE CODE: R154 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090521 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090521 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090521 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100521 Year of fee payment: 6 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100521 Year of fee payment: 6 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110521 Year of fee payment: 7 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120521 Year of fee payment: 8 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313117 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120521 Year of fee payment: 8 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120521 Year of fee payment: 8 |
|
LAPS | Cancellation because of no payment of annual fees | ||
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
EXPY | Cancellation because of completion of term |