JPH01218619A - Dehumidifying agent - Google Patents
Dehumidifying agentInfo
- Publication number
- JPH01218619A JPH01218619A JP4413688A JP4413688A JPH01218619A JP H01218619 A JPH01218619 A JP H01218619A JP 4413688 A JP4413688 A JP 4413688A JP 4413688 A JP4413688 A JP 4413688A JP H01218619 A JPH01218619 A JP H01218619A
- Authority
- JP
- Japan
- Prior art keywords
- gypsum
- copper sulfate
- dehumidifying agent
- agent
- dehumidifying
- 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
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims abstract description 24
- 229910000365 copper sulfate Inorganic materials 0.000 claims abstract description 18
- 239000010440 gypsum Substances 0.000 claims abstract description 13
- 229910052602 gypsum Inorganic materials 0.000 claims abstract description 13
- 239000002274 desiccant Substances 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 10
- 238000007791 dehumidification Methods 0.000 abstract description 7
- 238000006477 desulfuration reaction Methods 0.000 abstract description 4
- 230000023556 desulfurization Effects 0.000 abstract description 4
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract description 2
- 239000003546 flue gas Substances 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 229920006395 saturated elastomer Polymers 0.000 abstract description 2
- 150000004683 dihydrates Chemical class 0.000 abstract 2
- 238000000151 deposition Methods 0.000 abstract 1
- 238000004898 kneading Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229910021536 Zeolite Inorganic materials 0.000 description 3
- 229910001628 calcium chloride Inorganic materials 0.000 description 3
- 239000001110 calcium chloride Substances 0.000 description 3
- 235000011148 calcium chloride Nutrition 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 239000010457 zeolite Substances 0.000 description 3
- 235000015895 biscuits Nutrition 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000008235 industrial water Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 235000012495 crackers Nutrition 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011508 lime plaster Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Drying Of Gases (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は新規な脱湿剤に関し、特にCo、レーザ発振媒
体ガスや天然ガス等工業用ガスの脱湿、禁湿性精密機械
、鋼材等の保管、輸送時の除湿、部屋や衣服箱の乾燥、
禁湿性食品(のシ、ビスケット、クラッカー)等の乾燥
用などに使用される脱湿剤に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a new dehumidifying agent, particularly for dehumidifying industrial gases such as Co, laser oscillation medium gas and natural gas, moisture-proof precision machinery, steel materials, etc. Dehumidifying during storage and transportation, drying rooms and clothes boxes,
This product relates to a desiccant used for drying moisture-proof foods (such as biscuits, biscuits, and crackers).
従来の脱湿剤としては、塩化カルシウム、硫酸銅、ゼオ
ライ1−、シリカゲル等が使用されている。As conventional desiccants, calcium chloride, copper sulfate, zeolite 1-, silica gel, etc. are used.
塩化カルシウムはCaC4・2H20と表わされ、30
0°C近傍で加熱すると脱水し、無水塩化カルシウム(
CaCl2)となシ、脱湿剤として使用されるものであ
るが、このものは粉体であって、利用にあたっては充填
、取シ出し時の取扱いが不便であシ、さらに粉体である
ため脱湿時のガス接触に際しては圧力損失が大であると
いう欠点がある。また潮解性があるため有効に利用され
る比率が少ない上に、機械部品などに接触すると腐食な
どの原因となる欠点があり用途に限界がある。Calcium chloride is expressed as CaC4.2H20 and is 30
When heated near 0°C, it dehydrates and forms anhydrous calcium chloride (
CaCl2) is used as a dehumidifying agent, but since it is a powder, handling during filling and unloading is inconvenient; There is a drawback that pressure loss is large when contacting gas during dehumidification. Furthermore, because of its deliquescent properties, it is rarely used effectively, and it also has the drawback of causing corrosion when it comes into contact with mechanical parts, which limits its use.
硫酸銅は通常CuSO4* 5H10と表わされ、15
0℃以上に加熱すると脱水し、無水硫酸銅(Cu80n
)とな)、強力な脱湿剤として使用されるものであるが
、このものは粉体であって、利用にあたっては充填、取
り出し時の取扱いが不便であ択さらに粉体であるため脱
湿剤のガス接触に際しては塩化力μシウムと同様に圧力
損失が大であるという欠点がある。まだ、このものは吸
収剤としての利用率も悪いという欠点をも有しているば
かりでなく、ゼオライトやシリカゲルに対比して高価で
あるという問題もある。Copper sulfate is usually expressed as CuSO4*5H10, 15
When heated above 0°C, it dehydrates and becomes anhydrous copper sulfate (Cu80n).
) is used as a strong dehumidifying agent, but since it is a powder, it is inconvenient to handle when filling and taking out, and since it is a powder, it is not suitable for dehumidification. When the agent is brought into contact with a gas, it has the disadvantage of a large pressure loss, similar to the case with μsium chloride. However, this material not only has the disadvantage of poor utilization as an absorbent, but also has the problem of being expensive compared to zeolite and silica gel.
又、ゼオライトやシリカゲルは水分の他にCo、などの
極性物質の共吸着があり不都合であるという問題があっ
た。In addition, zeolite and silica gel have the disadvantage that they co-adsorb polar substances such as Co in addition to water.
本発明は上述の技術水準に鑑み、安価で脱湿容量が大き
く、かつ再生の容易な脱湿剤を提供しようとするもので
ある。In view of the above-mentioned state of the art, the present invention aims to provide a desiccant agent that is inexpensive, has a large dehumidifying capacity, and is easily regenerated.
本発明は硫酸銅を石膏に担持してなることを特徴とする
脱湿剤である。The present invention is a desiccant agent characterized in that copper sulfate is supported on gypsum.
本発明において担体として使用する石膏は、石灰石膏法
の脱硫プロセスなどによっても得ることのできる極めて
安価な材料である。また、この石膏も百数十度に加熱す
ると工水塩(CuSO4−2H!0 )から半水塩(C
aS04・%H,O)に転化し、この半水塩も水分の存
在下では工水塩に復元するので脱湿剤としても作用する
。またこの作用の他に粉体である硫酸銅の成形用粘結剤
としての効果をもつという利点がある。Gypsum used as a carrier in the present invention is an extremely inexpensive material that can also be obtained by a desulfurization process using the lime plaster method. Also, when this gypsum is heated to over 100 degrees, it changes from industrial water salt (CuSO4-2H!0) to hemihydrate salt (C
aS04.%H,O), and this hemihydrate salt is also restored to industrial water salt in the presence of moisture, so it also acts as a desiccant agent. In addition to this effect, copper sulfate, which is a powder, has the advantage of being effective as a molding binder.
本発明の脱湿剤における石膏と硫酸銅の重量比は、石膏
:硫酸銅=100:20〜5oの範囲が好ましい。硫酸
銅をこの量販下にすると強度は向上するものの脱湿効果
が低下し、またこの量販上であると脱湿効果は向上する
□ものの強度が低下するからである。実用的には石膏1
00重量部に対し硫酸銅を50重量部に近い量で使用す
るのが好ましい。The weight ratio of gypsum to copper sulfate in the desiccant of the present invention is preferably in the range of gypsum:copper sulfate=100:20 to 5o. This is because if copper sulfate is sold in large quantities, the strength will be improved but the dehumidifying effect will be reduced, and if copper sulfate is sold in such large quantities, the dehumidifying effect will be improved but the strength will be reduced. Practically speaking, plaster 1
It is preferred to use copper sulfate in an amount close to 50 parts by weight per 00 parts by weight.
以下、従来の硫酸銅単独の脱湿剤を比較例としてあげ、
本発明の脱湿剤の一実施例をそれと対比して説明する。Below, a conventional dehumidifier containing copper sulfate alone is given as a comparative example.
An embodiment of the desiccant of the present invention will be explained in comparison thereto.
比較脱湿剤として、試薬−級のCu S 04・5H!
0の粉末を、そのま−160°Cで3時間加熱して無水
硫酸銅CuSO4とした。(この5H80の飛散温度は
150℃である)これをガラス管に充填し、その充填物
に30℃の水と接触させることによって調製した含水空
気(約Q、42%)を流通させ、脱湿を行なった。最初
はその脱湿剤で処理された空気中にはほとんど水分は含
くまれていなかったが、そのうち吸湿能力の低下ととも
に水分が残留するようになった。水分の残留濃度がQ、
1容量%となった時点で脱湿剤の重量を測定し、理論吸
湿量をCuSO4・5H20まで吸収するとして計算す
ると理論量の23%だけ吸水していた。即ち充填したC
uSO4の77%が未反応でありCuSO4の利用率は
悪かった。As a comparative desiccant agent, reagent-grade Cu S 04.5H!
The powder of No. 0 was directly heated at -160°C for 3 hours to obtain anhydrous copper sulfate CuSO4. (The scattering temperature of this 5H80 is 150°C.) This was filled into a glass tube, and water-containing air (approximately Q, 42%) prepared by contacting the filled material with water at 30°C was passed through to dehumidify it. I did it. Initially, the air treated with the desiccant contained almost no moisture, but over time, as the moisture absorption capacity decreased, moisture began to remain. The residual concentration of water is Q,
The weight of the desiccant was measured when the moisture content reached 1% by volume, and calculation was made assuming that the theoretical amount of moisture absorbed was up to CuSO4.5H20, and the amount of water absorbed was 23% of the theoretical amount. That is, the filled C
77% of uSO4 was unreacted, and the utilization rate of CuSO4 was poor.
これに対し、排煙脱硫装置から生成した工水石膏(Cu
SO4−2FI、O)を150°Cで3時間加熱し半水
石膏を得た。これに硫酸銅(CuSO4・5H,O)と
して50重量%含有するように予め、水に溶解した水溶
液を半水石膏と混合し、十分混練したのち固化させ、こ
れを160°C,5時間加熱して脱湿剤とした。On the other hand, industrial gypsum (Cu) produced from flue gas desulfurization equipment
SO4-2FI, O) was heated at 150°C for 3 hours to obtain gypsum hemihydrate. An aqueous solution previously dissolved in water containing 50% by weight of copper sulfate (CuSO4.5H,O) was mixed with gypsum hemihydrate, thoroughly kneaded, solidified, and heated at 160°C for 5 hours. It was used as a dehumidifier.
比較例と同様30°Cの水で増湿した空気によシ脱湿試
験を行ない、処理ガス中に0.1容量%の水分が残留す
る時点でCuSO4の反応率を計算すると理論値の77
%であった。即ちCuSO4の未反応分は23%と大巾
なCu S 04の利用率の向上が認められた。この脱
湿剤中の石膏が仮シに半分吸湿したとしても硫酸銅単独
のもの(比較例)より利用率が高く、石膏との組合せ効
果が見られる。As in the comparative example, a dehumidification test was performed using air humidified with 30°C water, and when the reaction rate of CuSO4 was calculated at the point when 0.1% by volume of water remained in the treated gas, the theoretical value was 77.
%Met. That is, the unreacted portion of CuSO4 was 23%, and a significant improvement in the utilization rate of CuSO4 was observed. Even if the gypsum in this desiccant absorbs half of the moisture, the utilization rate is higher than that of copper sulfate alone (comparative example), and the effect of the combination with gypsum can be seen.
この脱湿剤は脱湿能の高い時は白色であり、水分の飽和
吸着時点ではCuSO4・5 H,O特有の青色となる
ため、再生時を指示する便利さがある。This dehumidifying agent is white when its dehumidifying ability is high, and becomes blue, which is characteristic of CuSO4.5 H,O, when moisture is saturated and adsorbed, so it is convenient to indicate when it is time to regenerate.
また飽和状態まで使用した後に160℃で加熱処理する
と脱湿能を回復することもわかった。It was also found that the dehumidification ability was recovered by heat treatment at 160° C. after use to saturation.
本発明の脱湿剤は、水分の吸着容量が大きく、再生可能
であるほか、脱湿能力の終点が色の変化で判定できるの
で、工業的に極めて有意義な脱湿剤である。The dehumidifying agent of the present invention has a large moisture adsorption capacity, is recyclable, and the end point of dehumidifying ability can be determined by a change in color, so it is an industrially extremely useful dehumidifying agent.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4413688A JPH01218619A (en) | 1988-02-29 | 1988-02-29 | Dehumidifying agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4413688A JPH01218619A (en) | 1988-02-29 | 1988-02-29 | Dehumidifying agent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01218619A true JPH01218619A (en) | 1989-08-31 |
Family
ID=12683213
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4413688A Pending JPH01218619A (en) | 1988-02-29 | 1988-02-29 | Dehumidifying agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01218619A (en) |
-
1988
- 1988-02-29 JP JP4413688A patent/JPH01218619A/en active Pending
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