JPH01242126A - Method and device for treating ozone - Google Patents
Method and device for treating ozoneInfo
- Publication number
- JPH01242126A JPH01242126A JP63065770A JP6577088A JPH01242126A JP H01242126 A JPH01242126 A JP H01242126A JP 63065770 A JP63065770 A JP 63065770A JP 6577088 A JP6577088 A JP 6577088A JP H01242126 A JPH01242126 A JP H01242126A
- Authority
- JP
- Japan
- Prior art keywords
- ozone
- hollow cylindrical
- gas
- treated
- humidity
- 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
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 title claims abstract description 76
- 238000000034 method Methods 0.000 title claims description 34
- 239000003054 catalyst Substances 0.000 claims abstract description 29
- 238000011282 treatment Methods 0.000 claims abstract description 29
- 239000000835 fiber Substances 0.000 claims abstract description 14
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 11
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 11
- 239000012784 inorganic fiber Substances 0.000 claims abstract description 10
- 239000000463 material Substances 0.000 claims description 26
- 238000000354 decomposition reaction Methods 0.000 claims description 12
- 238000012545 processing Methods 0.000 claims description 12
- 239000002952 polymeric resin Substances 0.000 claims description 10
- 229920000620 organic polymer Polymers 0.000 claims description 7
- 229920003002 synthetic resin Polymers 0.000 claims description 4
- 238000005273 aeration Methods 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 3
- 239000002699 waste material Substances 0.000 abstract description 8
- 230000003197 catalytic effect Effects 0.000 abstract description 4
- 239000006227 byproduct Substances 0.000 abstract description 2
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 51
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 18
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 8
- 229910052748 manganese Inorganic materials 0.000 description 8
- 239000011572 manganese Substances 0.000 description 8
- 238000009423 ventilation Methods 0.000 description 8
- 239000004576 sand Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000004891 communication Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000004887 air purification Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- HSSJULAPNNGXFW-UHFFFAOYSA-N [Co].[Zn] Chemical compound [Co].[Zn] HSSJULAPNNGXFW-UHFFFAOYSA-N 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000010800 human waste Substances 0.000 description 1
- 229920000592 inorganic polymer Polymers 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
Landscapes
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Catalysts (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、水処理や空気浄化等の目的で利用されるオゾ
ン処理から排出される廃オゾン、および各種放電管から
副生されるオゾンを除去する方法と装置に関するもので
ある。[Detailed Description of the Invention] [Industrial Application Field] The present invention is designed to treat waste ozone discharged from ozone treatment used for purposes such as water treatment and air purification, and ozone by-produced from various discharge tubes. The present invention relates to a method and apparatus for removing the present invention.
オゾンの利用は、水処理、殺菌、空気浄化などの分野を
中心に今後ますます増加するとみられるが、排ガス中に
はオゾンが残留している。また、各種放電管からはオゾ
ンが副生されそのまま排出される。これらの排出される
オゾンは、大気汚染に係る環境基準をはるかに越えた値
になることが多く、その処理が必要である。The use of ozone is expected to increase in the future, mainly in fields such as water treatment, sterilization, and air purification, but ozone remains in exhaust gas. Further, ozone is produced as a by-product from various discharge tubes and is discharged as is. The emitted ozone often exceeds environmental standards for air pollution, and must be treated.
従来、廃オゾンの処理技術には、活性炭法、薬液吸収法
、熱分解法、触媒法などがあった。Conventional technologies for treating waste ozone include activated carbon methods, chemical absorption methods, thermal decomposition methods, and catalytic methods.
活性炭法は、オゾンを活性炭充填層に導き、203+C
”→30!+C”
但しC0は活性炭
なる反応によってオゾンを分解するものであり、この方
法は低濃度のオゾンを効率良く分解できるために幅広く
利用されている。The activated carbon method introduces ozone into an activated carbon packed bed and generates 203+C
"→30!+C" However, C0 is a method that decomposes ozone through a reaction called activated carbon, and this method is widely used because it can efficiently decompose low concentrations of ozone.
薬液吸収法は、亜硫酸ナトリウム、チオ硫酸ナトリウム
、第1鉄塩などの還元剤水溶液、または水酸化ナトリウ
ムなどのアルカリ水溶液にオゾンを吸収させる方法であ
る。The chemical absorption method is a method in which ozone is absorbed into an aqueous reducing agent solution such as sodium sulfite, sodium thiosulfate, or ferrous salt, or an alkaline aqueous solution such as sodium hydroxide.
熱分解法は、重油、軽油などの燃焼室へオゾンを導いて
熱分解する方法である。The pyrolysis method is a method for thermally decomposing heavy oil, light oil, etc. by introducing ozone into the combustion chamber.
さらに触媒法は、例えば二酸化マンガンを主成分とした
ものでは、砂の表面にマンガン酸化物を付着させたもの
、シリカ・アルミナ質ゲル、粘土。Furthermore, catalytic methods include methods that use manganese dioxide as the main component, such as manganese oxide attached to the surface of sand, silica/alumina gel, and clay.
活性炭などとマンガン酸化物とを混合して焼成したもの
などの粒状触媒の充填層にオゾンを導き、主として
203+M、lO□→30□ +H,IO!の反応によ
りオゾンを分解するものである。Ozone is introduced into a packed bed of a granular catalyst such as a mixture of activated carbon and manganese oxide and calcined, and mainly 203+M, 1O□ → 30□ +H,IO! This reaction decomposes ozone.
しかしながら、前記従来のオゾンの処理技術には次のよ
うな欠点があった。However, the conventional ozone treatment technology has the following drawbacks.
活性炭法の欠点としては、オゾンとの反応に伴う活性炭
粒子の粉化、副反応として一酸化炭素や二酸化炭素に酸
化されることによる活性炭の減少。Disadvantages of the activated carbon method include powdering of activated carbon particles due to reaction with ozone, and reduction of activated carbon due to oxidation to carbon monoxide and carbon dioxide as a side reaction.
高濃度オゾンと接触させた場合の着火や増発の危険性な
どが挙げられている。The dangers of ignition and increased explosion when coming into contact with high-concentration ozone are cited.
薬液吸収法の場合は、オゾン吸収により薬液の組成が変
化するために吸収能力が低下すること、そのために薬液
の補充や廃液の処理が必要であり、煩雑であることなど
が挙げられている。In the case of the chemical absorption method, the absorption capacity decreases due to changes in the composition of the chemical due to ozone absorption, which requires replenishment of the chemical and treatment of waste liquid, which is complicated.
熱分解法は、活性炭処理では爆発の危険があるような高
濃度のオゾンを処理する場合に良(実施されるが、コス
トが高い。The pyrolysis method is suitable for treating high concentrations of ozone where activated carbon treatment poses a risk of explosion, but it is expensive.
また触媒法は、触媒のオゾン分解性能が低く、処理速度
を大きくできない。In addition, in the catalyst method, the ozone decomposition performance of the catalyst is low, and the processing speed cannot be increased.
本発明は触媒法を利用するものであるが、従来のものに
比べて格段に大きな表面積をもった特定の触媒を用い、
大きな通気速度でかつ安全性高く経済的なオゾン処理を
可能とし、さらに装置を小型軽量化し、コンパクトでメ
ンテナンスを容易にすることを可能としたオゾン処理方
法及びオゾン処理装置を提供することを目的とするもの
である。The present invention utilizes a catalytic method, but uses a specific catalyst with a much larger surface area than conventional ones.
The purpose of the present invention is to provide an ozone treatment method and an ozone treatment device that enable safe and economical ozone treatment at a high ventilation rate, and that also make the device smaller and lighter, making it compact and easy to maintain. It is something to do.
本発明は、無機系繊維又は有機系高分子樹脂繊維の表面
に金属酸化物触媒を担持せしめたろ過材の充填層にオゾ
ンを含有する被処理ガスを通気するに際し、該被処理ガ
スの比較湿度を80%以下に調整して通気することを特
徴とするオゾン処理方法である。The present invention provides a comparative humidity level of the gas to be treated when passing the gas to be treated containing ozone through a packed layer of a filter material having a metal oxide catalyst supported on the surface of inorganic fibers or organic polymeric resin fibers. This ozone treatment method is characterized by adjusting the temperature to 80% or less and venting.
また本発明は、オゾンを含有する被処理ガスを流入せし
める流入口を備えた湿度調整室と、無機系繊維又は有機
系高分子樹脂繊維の表面に金属酸化物触媒を担持せしめ
て中空筒状に成形したろ過材を収容したオゾン分解室と
からなり、該オゾン分解室内の前記中空筒状ろ過材の内
側又は外側を前記湿度調整室と連通せしめると共にオゾ
ン分解室に前記中空筒状ろ過材の外側又は内側に連通ず
る処理ガス流出口を設け、前記湿度調整室から流出する
被処理ガスが前記中空筒状ろ過材を1ffi過して前記
処理ガス流出口から流出するようにしたことを特徴とす
るオゾン処理装置であり、さらに本発明は、無機系繊維
又は有機系高分子樹脂繊維の表面に金属酸化物触媒を担
持せしめて中空筒状に成形したろ過材を容器内に収容し
、該中空筒状ろ過材の内側又は外側周囲に湿度調整器を
配備し、前記容器にオゾンを含有する被処理ガスの流入
口を設けて前記湿度調整器に連通せしめると共に容器に
前記中空筒状ろ過材の外側又は内側に連通ずる処理ガス
流出口を設け、前記湿度調整器から流出する被処理ガス
が前記中空筒状ろ過材を通過して前記処理ガス流出口か
ら流出するようにしたことをvF欲とするオゾン処理装
置である。The present invention also provides a humidity control chamber equipped with an inlet for introducing a gas to be treated containing ozone, and a hollow cylindrical structure in which a metal oxide catalyst is supported on the surface of an inorganic fiber or an organic polymer resin fiber. an ozone decomposition chamber containing a molded filter medium, and the inside or outside of the hollow cylindrical filter medium in the ozone decomposition chamber is communicated with the humidity adjustment chamber, and the outside of the hollow cylindrical filter medium is connected to the ozone decomposition chamber. Alternatively, a process gas outlet communicating with the inside is provided, and the process gas flowing out from the humidity adjustment chamber passes through the hollow cylindrical filter medium by 1ffi and flows out from the process gas outlet. The present invention is an ozone treatment device, and the present invention further provides an ozone treatment device in which a filter material formed into a hollow cylinder shape by supporting a metal oxide catalyst on the surface of inorganic fibers or organic polymer resin fibers is housed in a container, and the hollow cylinder A humidity regulator is installed around the inside or outside of the hollow cylindrical filter medium, and an inlet for the ozone-containing gas to be treated is provided in the container to communicate with the humidity adjuster, and a humidity controller is provided around the outside of the hollow cylindrical filter medium. Alternatively, a process gas outlet communicating with the inside is provided, and the process gas flowing out from the humidity regulator passes through the hollow cylindrical filter material and flows out from the process gas outlet. This is an ozone treatment device.
本発明では、ガラス、金属などの無機系の又は有機系高
分子樹脂の繊維状、スポンジ状、y4状。In the present invention, inorganic or organic polymer resins such as glass and metals are used in the fibrous, sponge, and Y4 shapes.
フェルト状等の繊維を担体とし、この担体表面にマンガ
ン、ニッケル、コバルト、銅、m、 亜鉛等の金属酸化
物触媒の単数又は複数を担持せしめたろ過材、好ましく
はマンガン酸化物単体又はマンガン酸化物を他の金属酸
化物と共に担持せしめたろ過材の充填層を使用すること
から、その比表面積を0. O05rd/cs3以上と
従来の粒状触媒にはなかった格段に大きな表面積とし、
この充填層へオゾンを含有する被処理ガスを通気するこ
とによって、従来にない薄い層厚で大きな通気速度によ
る処理が可能となる。A filter material having a felt-like fiber as a carrier and carrying one or more metal oxide catalysts such as manganese, nickel, cobalt, copper, m, zinc, etc. on the surface of the carrier, preferably manganese oxide alone or manganese oxide. Since we use a packed bed of filter material that supports substances together with other metal oxides, its specific surface area can be reduced to 0. With a surface area of O05rd/cs3 or more, which is not found in conventional granular catalysts,
By ventilating a gas to be treated containing ozone into this packed bed, it becomes possible to perform processing at a high ventilation rate with a thin layer thickness that was previously unheard of.
なお、被処理ガスの比較湿度が80%以下の場合には問
題はないが、被処理ガスに同伴される水分が増すに従っ
てオゾンの分解が不十分となる傾向が生じる。この問題
は触媒たるろ過材の表面が水分で濡れることによって被
処理ガス七の接触が阻害されることに起因している。こ
れを防ぐためには、被処理ガスの比較湿度が80%以上
の場合には、加温、冷却除湿、除湿剤による除湿等によ
ってその比較湿度を80%以下に調整して水分の結露を
防止して通気処理することが必要である。Note that there is no problem when the relative humidity of the gas to be treated is 80% or less, but as the amount of moisture accompanying the gas to be treated increases, the decomposition of ozone tends to become insufficient. This problem is caused by the fact that the surface of the filter material, which is a catalyst, becomes wet with moisture, which inhibits contact with the gas to be treated. To prevent this, if the comparative humidity of the gas to be treated is 80% or higher, adjust the comparative humidity to 80% or lower by heating, cooling and dehumidifying, dehumidifying with a dehumidifier, etc. to prevent water condensation. It is necessary to carry out ventilation treatment.
また、前記ろ過材の充填層としては、中空筒状に成形し
たものが良く、この中空筒状ろ過材の内側から外側へ、
あるいは外側から内側へ、比較湿度80%以下の被処理
ガスを通気することによって、従来にない薄い層厚及び
大きな通気速度、例えば中空筒状ろ過材の厚さ50〜2
00tsでSV2、000〜10,000 Nlll3
−被処理ガス/麟3−ろ過材・hの通気速度による効果
的な処理が可能になる。In addition, the packed layer of the filter medium is preferably formed into a hollow cylindrical shape, and from the inside to the outside of this hollow cylindrical filter medium,
Alternatively, by ventilating the gas to be treated with a comparative humidity of 80% or less from the outside to the inside, it is possible to achieve an unprecedentedly thin layer thickness and high aeration rate, for example, when the thickness of the hollow cylindrical filter material is 50 to 2.
00ts SV2, 000~10,000 Nlll3
- Gas to be treated / Rin 3 - Effective treatment is possible by adjusting the ventilation rate of the filter material/h.
本発明の装置の例について図面を参照しながら説明する
と、第1図において、■は湿度調整室で内部には湿度調
整器例えばヒーター2が配備され、3はオゾン分解室で
内部には、ガラス、金属などの無機系の又は有機系高分
子樹脂の繊維状、スポンジ状、′4F4状、フェルト状
等の繊維を担体とし、この担体表面にマンガン、ニッケ
ル、コバルト。An example of the apparatus of the present invention will be explained with reference to the drawings. In FIG. The carrier is made of inorganic or organic polymeric resin fibers such as metals, sponge-like, '4F4-like, felt-like fibers, etc., and manganese, nickel, and cobalt are applied to the surface of the carrier.
銅、銀、亜鉛等の金属酸化物触媒の単数又は複数を担持
せしめて中空筒状に成形したろ過材4が収容されている
。A filter medium 4 formed into a hollow cylindrical shape and supported with one or more metal oxide catalysts such as copper, silver, and zinc is accommodated.
湿度調整室lには、オゾンを含有する被処理ガスの流入
管5とオゾン分解室3に連通する連通管6が連結され、
流入管5から流入した被処理ガスがヒーター2によって
加温され、被処理ガスの比較湿度を80%以下に調整で
きるようになっている。Y!度調整室lの連通管6は、
オゾン分解室3内の中空筒状ろ過材4の内側に連通され
、またオゾン分解室3には中空筒状ろ過材4の外側に連
通ずる処理ガス流出管7が連結されている。An inflow pipe 5 for the gas to be treated containing ozone and a communication pipe 6 communicating with the ozone decomposition chamber 3 are connected to the humidity adjustment chamber l,
The gas to be treated that flows in from the inflow pipe 5 is heated by the heater 2, so that the relative humidity of the gas to be treated can be adjusted to 80% or less. Y! The communication pipe 6 of the temperature adjustment chamber l is
A process gas outflow pipe 7 is connected to the inside of the hollow cylindrical filter material 4 in the ozone decomposition chamber 3 and to the outside of the hollow cylindrical filter material 4 .
図中、8は湿度調整室1の連通管6の室内開口部を覆う
短絡防止用の邪魔板を示し、9はオゾン分解室3内部で
被処理ガスを中空筒状ろ過材4へ誘導するための邪魔板
を示す。In the figure, 8 indicates a baffle plate for preventing short circuits that covers the indoor opening of the communication pipe 6 of the humidity adjustment chamber 1, and 9 indicates a baffle plate for guiding the gas to be treated to the hollow cylindrical filter material 4 inside the ozone decomposition chamber 3. This shows the baffle plate.
第2図の例では、容器11内の中空筒状ろ過材4の内側
に温度調整器たるヒーター2を配備し、容器11には被
処理ガスの流入管5がヒーター2に連通ずるように連結
される一方、処理ガス流出管7が中空筒状ろ過材4の外
側に連通ずるように連結されている。In the example shown in FIG. 2, a heater 2 serving as a temperature regulator is provided inside a hollow cylindrical filter material 4 in a container 11, and an inflow pipe 5 for the gas to be treated is connected to the container 11 so as to communicate with the heater 2. On the other hand, a processing gas outflow pipe 7 is connected to the outside of the hollow cylindrical filter material 4 so as to communicate therewith.
これら図示例の装置において、オゾンを含有する被処理
ガスは、流入管5から湿度調整室1内又は容器11内に
流入し、ヒーター2によって加温され比較湿度80%以
下に調整されてガス中の水分の結露が防止され、中空筒
状ろ過材4の内側から外側へ通気されてガス中のオゾン
が分解処理され、処理ガス流出管7から流出する。In these illustrated apparatuses, the gas to be treated containing ozone flows into the humidity adjustment chamber 1 or the container 11 from the inflow pipe 5, is heated by the heater 2, and is adjusted to a relative humidity of 80% or less, and is then contained in the gas. The ozone in the gas is decomposed by being vented from the inside to the outside of the hollow cylindrical filter medium 4, and then flows out from the treated gas outflow pipe 7.
この場合、ろ過材の被表面積は0.005 m”/ c
m”以上と大きく、しかも中空筒状に成形されているた
めに、層厚50〜200tmという薄層で圧力損失を大
きくすることなく 、SV 2,000〜10.000
HIII!−被処理ガス/醜3−ろ過材・hという大
きな通気速度での処理が可能であり、従来の粒状触媒で
は得られない高速処理を可能にする。In this case, the surface area of the filter medium is 0.005 m”/c
2,000 to 10,000 without increasing pressure loss even with a thin layer of 50 to 200 tm.
HIII! - Gas to be treated / Ugly 3 - Processing at a high aeration rate of 3-filter material / h is possible, enabling high-speed processing that cannot be achieved with conventional granular catalysts.
なお、前記第1図の例では、オゾン分解室3内の被処理
ガスの流れを、中空筒状ろ過材4の内側から外側に1J
Il遇させて処理ガス流出管7から流出しているが、湿
度調整室1から流出する被処理ガスを中空筒状ろ過材4
の外側に導き、内側へij1遇させて処理ガス流出管7
から流出するような構成にすることができる。In the example shown in FIG.
However, the gas to be treated flowing out from the humidity adjustment chamber 1 is filtered through the hollow cylindrical filter material 4.
The process gas outlet pipe 7 is guided to the outside and directed to the inside.
It can be configured so that it flows from the
また、前記第2図の例でも、被処理ガスの流れを、ヒー
ター2を経て中空筒状ろ過材4の内側から外側に通過さ
せて処理ガス流出管7から流出しているが、ヒーター2
を中空筒状ろ過材4の外側周囲に配設し、被処理ガスを
ヒーター2を経て中空筒状ろ過材4の外側から内側に通
過させて処理ガス流出管7から流出するような構成にす
ることもできる。Furthermore, in the example shown in FIG. 2, the flow of the gas to be treated passes through the heater 2 from the inside to the outside of the hollow cylindrical filter medium 4 and flows out from the process gas outlet pipe 7.
is disposed around the outside of the hollow cylindrical filter material 4, and the gas to be treated passes through the heater 2 from the outside to the inside of the hollow cylindrical filter material 4, and is configured to flow out from the treated gas outflow pipe 7. You can also do that.
次に実験例を示す。Next, an experimental example will be shown.
(実験例1)
Aし尿処理場で排出された廃オゾンガスを対象として行
った本発明の処理例を示す。(Experimental Example 1) An example of the treatment of the present invention performed on waste ozone gas discharged at a human waste treatment plant A will be shown.
廃オゾンガスの性状は、温度30℃、オゾン濃度6g/
Nrrl、絶対18度は0.299kg/賭′であり、
比較湿度は110%であった。The properties of waste ozone gas are: temperature 30℃, ozone concentration 6g/
Nrrl, absolute 18 degrees is 0.299 kg/bet',
The comparative humidity was 110%.
ろ過材たる触媒は、平均径0.311の有機系高分子樹
脂繊維にマンガン、コバルト、亜鉛の酸化物を担持せし
めて層厚200m1の中空円筒体に成形したもので、水
洗塔方式+加温方式によって廃オゾンガスの比較湿度を
20%に調整し、SVを変化させ中空円筒ろ過材の内側
から外側へ通気した。The catalyst used as the filter material is made by supporting manganese, cobalt, and zinc oxides on organic polymer resin fibers with an average diameter of 0.311 and molding them into a hollow cylindrical body with a layer thickness of 200 m1. The comparative humidity of the waste ozone gas was adjusted to 20% by the method, and the SV was changed to allow ventilation from the inside to the outside of the hollow cylindrical filter material.
これらの結果は下表に示す通りであって、5V=2.
OOO〜10.000 Nr+?/ffl・hの範囲で
オキシダントの環境基準である0、06シof、 pp
+w以下に処理されていた。These results are shown in the table below, and 5V=2.
OOO~10.000 Nr+? The environmental standard for oxidants in the range of /ffl・h is 0, 06 shof, pp
It was processed below +w.
さらに、原ガス及び触媒の条件を同一にし、5v=2.
000 Nrd/rd・hの処理において比較湿度を変
化させた場合の処理ガスオゾン濃度の変化を第3図に示
す。Furthermore, the raw gas and catalyst conditions were made the same, and 5v=2.
FIG. 3 shows changes in the ozone concentration of the treated gas when the relative humidity was changed in the treatment of 000 Nrd/rd·h.
オゾンの完全除去を行うためには比較湿度を20%程度
とすることが望ましいが、比較湿度80%まではオキシ
ダントの環境基準である0、06vo1. pp+s以
下に処理されており、80%を越えると処理は急速に悪
化した。In order to completely remove ozone, it is desirable to keep the relative humidity at around 20%, but the relative humidity up to 80% is 0.06vo1.0, which is the environmental standard for oxidants. It was processed to less than pp+s, and when it exceeded 80%, the processing deteriorated rapidly.
(実験例2)
紫外線ランプから副生されたオゾンガスを対象として行
った本発明の処理例を示す。(Experimental Example 2) An example of the treatment of the present invention performed on ozone gas by-produced from an ultraviolet lamp is shown.
オゾンガスの性状は、温度20℃、オゾン濃度10vo
1. ppm、比較湿度70%であった。The properties of ozone gas are: temperature 20℃, ozone concentration 10vo
1. ppm, and the comparative humidity was 70%.
ろ過材たる触媒は平均径0.05 曹mの無機系繊維に
マンガン、コバルト亜鉛の酸化物を担持させて層厚10
0111の充填層とし、この充填層に比較湿度は無調整
とし、Svを変化させてオゾンガスを通気した。The catalyst, which is the filter material, is made of inorganic fibers with an average diameter of 0.05 m and a layer thickness of 10 m, supporting oxides of manganese and cobalt zinc.
0111, and ozone gas was passed through the packed bed while changing the Sv without adjusting the comparative humidity.
これらの結果は下表に示す通りであり、湿度調整をする
ことなしニ5V=2,000〜10,0OONr+?/
n? ・hの範囲でオキシダントの環境基<Bである0
、06vo1. pps以下に処理されていた。These results are shown in the table below, and 5V = 2,000 to 10,0OONr+? without humidity adjustment. /
n?・0 where the environmental group of the oxidant <B in the range of h
, 06vo1. It was processed below pps.
(実験例3)
従来のマンガン砂を用いた場合と本発明による触媒を用
いた場合との圧力損失の比較を第4図に示す。(Experimental Example 3) FIG. 4 shows a comparison of pressure loss between the case where conventional manganese sand was used and the case where the catalyst according to the present invention was used.
第4図は触媒への通気線速度LV(Nn?/ n(−h
)と触媒loom厚あたりの圧力損失の関係を示した
ものであり、マンガン砂は有効径0.61、本発明■は
平均径0.05 l*の無機系繊維にマンガン酸化物を
担持せしめたもの、木穴明■は平均径0.3鶴の有機系
高分子繊維にマンガン酸化物を担持せしめたものである
。Figure 4 shows the linear velocity of ventilation to the catalyst LV (Nn?/n(-h
) and the pressure drop per catalyst loom thickness. Manganese sand has an effective diameter of 0.61, and the present invention (2) has manganese oxide supported on inorganic fibers with an average diameter of 0.05 l*. The product, Kiana Akira ■, is made by supporting manganese oxide on organic polymer fibers with an average diameter of 0.3.
この中では、繊維径0.3Hの本発明■の圧力を員失が
小さく、LV8ONrn’/m・hのとき、9IIt
to/ 100 m−触媒であった。ta維径径005
m1の本発明■の圧力を置火は■のおよそ2倍程度であ
った。Among these, the pressure of the invention
to/100 m-catalyst. ta fiber diameter 005
The pressure of ml of the present invention (2) was about twice that of (2).
これに対し、マンガン砂の圧力を置火はLV8 ONm
/n(・hの段階ですでに240Hzo/ 100 m
−触媒であり、マンガン砂による処理は通常層高600
〜1000mを要するため通気抵抗の面からもあまり高
速にできないことが分る。On the other hand, the pressure of manganese sand is LV8 ONm
/n(・h stage already 240Hz/100m
- catalyst, treatment with manganese sand usually has a bed height of 600
Since it requires ~1000m, it can be seen that it cannot be made very fast from the viewpoint of ventilation resistance.
また、マンガン砂による廃オゾンガス処理の例を第5図
に示すが、加温方式により比較湿度を20%に調整して
処理してもSvを40ON n? / ffl・hまで
小さくしないと処理できなかった。Furthermore, an example of waste ozone gas treatment using manganese sand is shown in Fig. 5, but even if the comparative humidity is adjusted to 20% using a heating method, Sv is still 40 ON n? /ffl・h could not be processed.
また本発明のオゾン処理装置形状の制限因子となるのは
廃ガスのオゾン濃度や処理S■ではなく、圧力I員失の
大きさにあると考えられる。したがって、処理ガス量が
大きい場合には断面積が大きく、層厚が小さいという充
填形式が必要となるため、単なる充填層の形式よりは中
空円筒状の形式とし、中空円筒の内側から外側へ、ある
いは外側から内側へ通気する形が存利である。Further, it is thought that the limiting factor for the shape of the ozone treatment apparatus of the present invention is not the ozone concentration of the waste gas or the treatment S, but the magnitude of the pressure loss. Therefore, when the amount of gas to be processed is large, a filling format with a large cross-sectional area and small layer thickness is required, so a hollow cylindrical format is used rather than a simple packed bed format, and Alternatively, it is advantageous to have a shape that allows ventilation from the outside to the inside.
〔発明の効果)
以上述べたように本発明によれば、使用するろ過材は無
機系繊維又は有機系高分子樹脂繊維の表面にマンガンそ
の他の金属酸化物触媒を担持させた極めて表面積の大き
いもので、圧力i置火低く、従来の粒状触媒では得られ
なかった高速処理が可能であり、さらに被処理ガスを比
較湿度80%以下に調整することによって効果的処理を
確実にし、安全性高く経済的であり、このろ過材を中空
筒状に成形することによって装置の小型化、軽量化を可
能とし、コンパクトでメンテナンスも容易となる等の多
(の有益なる効果を期待することができる。[Effects of the Invention] As described above, according to the present invention, the filtration medium used is one having an extremely large surface area, in which manganese or other metal oxide catalysts are supported on the surface of inorganic fibers or organic polymer resin fibers. The pressure and temperature are low, enabling high-speed processing that could not be achieved with conventional granular catalysts.Furthermore, by adjusting the relative humidity of the gas to be treated to less than 80%, effective treatment is ensured, making it highly safe and economical. By molding this filter material into a hollow cylindrical shape, the device can be made smaller and lighter, and many beneficial effects can be expected, such as making it compact and easy to maintain.
第1図及び第2図はそれぞれ本発明の装置の例を示す縦
断説明図、第3図は本発明における比較湿度と処理ガス
オゾン濃度の関係を示す線図、第4図は触媒へのLVと
触媒100酊厚あたりの圧力損失の関係を示す線図、第
5図は従来のマンガン砂を用いた場合のSvと処理ガス
オゾン濃度との関係を示す線図である。
■・・・湿度調節室、2・・・ヒーター、3・・・オゾ
ン分解室、4・・・中空筒状ろ過材、5・・・被処理ガ
スの流入管、6・・・連通管、7・・・処理ガス流出管
、8.9・・・邪魔板、11・・・容器。
特許出願人 荏原インフィルコ株式会社特許出願人
株式会社荏原総合研究所代理人 弁理士 薬
師 稔代理人 弁理士 依 1) 孝 次
部代理人 弁理士 高 木 正 行比較湿
度(χ)
第5図
5V(N myrm3−h)1 and 2 are longitudinal sectional views showing examples of the apparatus of the present invention, FIG. 3 is a diagram showing the relationship between relative humidity and ozone concentration of the treated gas in the present invention, and FIG. 4 is a diagram showing the relationship between the LV to the catalyst and the FIG. 5 is a diagram showing the relationship between pressure loss per 100 catalyst thicknesses, and FIG. 5 is a diagram showing the relationship between Sv and treated gas ozone concentration when conventional manganese sand is used. ■... Humidity control chamber, 2... Heater, 3... Ozone decomposition chamber, 4... Hollow cylindrical filter material, 5... Inflow pipe for gas to be treated, 6... Communication pipe, 7... Processing gas outflow pipe, 8.9... Baffle plate, 11... Container. Patent applicant Ebara Infilco Corporation Patent applicant
Ebara Research Institute Co., Ltd. Representative Patent Attorney Pharmaceutical
Teacher Minoru Agent Patent Attorney Yori 1) Takatsugu Department Agent Patent Attorney Tadashi Takagi Comparison Humidity (χ) Figure 5 5V (N myrm3-h)
Claims (3)
属酸化物触媒を担持せしめたろ過材の充填層にオゾンを
含有する被処理ガスを通気するに際し、該被処理ガスの
比較湿度を80%以下に調整して通気することを特徴と
するオゾン処理方法。(1) When passing the ozone-containing gas to be treated through a packed layer of a filter material in which a metal oxide catalyst is supported on the surface of inorganic fibers or organic polymeric resin fibers, the relative humidity of the gas to be treated is determined. An ozone treatment method characterized by adjusting the ozone concentration to 80% or less and aeration.
口を備えた湿度調整室と、無機系繊維又は有機系高分子
樹脂繊維の表面に金属酸化物触媒を担持せしめて中空筒
状に成形したろ過材を収容したオゾン分解室とからなり
、該オゾン分解室内の前記中空筒状ろ過材の内側又は外
側を前記湿度調整室と連通せしめると共にオゾン分解室
に前記中空筒状ろ過材の外側又は内側に連通する処理ガ
ス流出口を設け、前記湿度調整室から流出する被処理ガ
スが前記中空筒状ろ過材を通過して前記処理ガス流出口
から流出するようにしたことを特徴とするオゾン処理装
置。(2) A humidity control chamber equipped with an inlet through which a gas to be treated containing ozone flows, and a metal oxide catalyst supported on the surface of inorganic fibers or organic polymer resin fibers formed into a hollow cylindrical shape. an ozone decomposition chamber containing a filter medium, the inside or outside of the hollow cylindrical filter medium in the ozone decomposition chamber is communicated with the humidity adjustment chamber, and the ozone decomposition chamber is connected to the outside or inside of the hollow cylindrical filter medium. An ozone treatment apparatus characterized in that a processing gas outlet communicating with the humidity control chamber is provided, and the processing gas flowing out from the humidity adjustment chamber passes through the hollow cylindrical filter material and flows out from the processing gas outlet. .
属酸化物触媒を担持せしめて中空筒状に成形したろ過材
を容器内に収容し、該中空筒状ろ過材の内側又は外側周
囲に湿度調整器を配備し、前記容器にオゾンを含有する
被処理ガスの流入口を設けて前記湿度調整器に連通せし
めると共に容器に前記中空筒状ろ過材の外側又は内側に
連通する処理ガス流出口を設け、前記湿度調整器から流
出する被処理ガスが前記中空筒状ろ過材を通過して前記
処理ガス流出口から流出するようにしたことを特徴とす
るオゾン処理装置。(3) A filtration medium formed into a hollow cylindrical shape by supporting a metal oxide catalyst on the surface of inorganic fibers or organic polymeric resin fibers is housed in a container, and the inner or outer periphery of the hollow cylindrical filtration medium is accommodated. a humidity regulator is provided in the container, an inlet for a gas to be processed containing ozone is provided in the container to communicate with the humidity regulator, and a processing gas flow is provided in the container to communicate with the outside or inside of the hollow cylindrical filter material. An ozone treatment apparatus characterized in that an outlet is provided so that the treated gas flowing out from the humidity regulator passes through the hollow cylindrical filter material and flows out from the treated gas outlet.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63065770A JPH01242126A (en) | 1988-03-22 | 1988-03-22 | Method and device for treating ozone |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63065770A JPH01242126A (en) | 1988-03-22 | 1988-03-22 | Method and device for treating ozone |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2276192A Division JPH03143528A (en) | 1990-10-17 | 1990-10-17 | Treatment of ozone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01242126A true JPH01242126A (en) | 1989-09-27 |
| JPH0365213B2 JPH0365213B2 (en) | 1991-10-11 |
Family
ID=13296592
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63065770A Granted JPH01242126A (en) | 1988-03-22 | 1988-03-22 | Method and device for treating ozone |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01242126A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03109923A (en) * | 1989-09-26 | 1991-05-09 | Sakai Chem Ind Co Ltd | Catalytic filter |
| JPH0418352U (en) * | 1990-06-01 | 1992-02-17 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS514094A (en) * | 1974-07-01 | 1976-01-13 | Mitsubishi Heavy Ind Ltd | Ozonganjugasuchuno ozonbunkaijokyohoho |
| JPS5314688A (en) * | 1976-07-28 | 1978-02-09 | Toshiba Corp | Production of ozone decomposition catalyst |
| JPS56133029A (en) * | 1980-03-24 | 1981-10-17 | Ryomei Eng Corp Ltd | Filter for dezonizing |
| JPS62201648A (en) * | 1986-03-03 | 1987-09-05 | Nippon Shokubai Kagaku Kogyo Co Ltd | Catalyst for decomposing ozone |
-
1988
- 1988-03-22 JP JP63065770A patent/JPH01242126A/en active Granted
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS514094A (en) * | 1974-07-01 | 1976-01-13 | Mitsubishi Heavy Ind Ltd | Ozonganjugasuchuno ozonbunkaijokyohoho |
| JPS5314688A (en) * | 1976-07-28 | 1978-02-09 | Toshiba Corp | Production of ozone decomposition catalyst |
| JPS56133029A (en) * | 1980-03-24 | 1981-10-17 | Ryomei Eng Corp Ltd | Filter for dezonizing |
| JPS62201648A (en) * | 1986-03-03 | 1987-09-05 | Nippon Shokubai Kagaku Kogyo Co Ltd | Catalyst for decomposing ozone |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03109923A (en) * | 1989-09-26 | 1991-05-09 | Sakai Chem Ind Co Ltd | Catalytic filter |
| JPH0418352U (en) * | 1990-06-01 | 1992-02-17 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0365213B2 (en) | 1991-10-11 |
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