JPH0338247A - Deodorant - Google Patents
DeodorantInfo
- Publication number
- JPH0338247A JPH0338247A JP1174758A JP17475889A JPH0338247A JP H0338247 A JPH0338247 A JP H0338247A JP 1174758 A JP1174758 A JP 1174758A JP 17475889 A JP17475889 A JP 17475889A JP H0338247 A JPH0338247 A JP H0338247A
- Authority
- JP
- Japan
- Prior art keywords
- adsorption
- deodorant
- holes
- deodorizer
- deodorizing
- 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
- 239000002781 deodorant agent Substances 0.000 title abstract 6
- 230000001877 deodorizing effect Effects 0.000 abstract description 27
- 239000007789 gas Substances 0.000 abstract description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 6
- 230000003068 static effect Effects 0.000 abstract description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract description 4
- 150000001299 aldehydes Chemical class 0.000 abstract description 3
- 229910021529 ammonia Inorganic materials 0.000 abstract description 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 3
- 239000000194 fatty acid Substances 0.000 abstract description 3
- 229930195729 fatty acid Natural products 0.000 abstract description 3
- 150000004665 fatty acids Chemical class 0.000 abstract description 3
- 229910000037 hydrogen sulfide Inorganic materials 0.000 abstract description 3
- 238000012423 maintenance Methods 0.000 abstract description 3
- 229910017464 nitrogen compound Inorganic materials 0.000 abstract description 3
- 150000002830 nitrogen compounds Chemical class 0.000 abstract description 3
- 150000003464 sulfur compounds Chemical class 0.000 abstract description 3
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 abstract description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract description 2
- 150000001412 amines Chemical class 0.000 abstract description 2
- -1 ammonia and amines Chemical compound 0.000 abstract description 2
- 238000010276 construction Methods 0.000 abstract description 2
- 230000007423 decrease Effects 0.000 abstract description 2
- 150000002576 ketones Chemical class 0.000 abstract description 2
- 238000001179 sorption measurement Methods 0.000 description 44
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 24
- 239000003795 chemical substances by application Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 8
- 238000009423 ventilation Methods 0.000 description 8
- 238000010586 diagram Methods 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 239000003518 caustics Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004332 deodorization Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000007084 catalytic combustion reaction Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000010800 human waste Substances 0.000 description 1
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical class Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Treating Waste 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]
本発明は脱臭剤に貫通孔を設け、充填量を増大すること
なく圧力損失を低下させた脱臭剤に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a deodorizer that is provided with through holes and that reduces pressure loss without increasing the filling amount.
し尿処理場、下水処理場、ゴミ処理場等のサービス業や
化学工場、病院などにおいて、臭覚闇値の低い硫化水素
、メルカプタンなどのイオウ化合物、アンモニア、アミ
ン類の窒素化合物、さらに低級脂肪酸類、アルデヒド類
等を多量に含有する悪臭ガスが発生する事は周知の如く
である。In service industries such as human waste treatment plants, sewage treatment plants, and garbage treatment plants, as well as chemical factories and hospitals, sulfur compounds such as hydrogen sulfide and mercaptan, ammonia, and nitrogen compounds such as amines, lower fatty acids, It is well known that foul-smelling gas containing a large amount of aldehydes and the like is generated.
これらの悪臭ガスの脱臭方法としては、(1)酸、アル
カリ液による洗滌吸収方法(2)過マンガン酸カリ、次
亜塩素酸塩類、オゾンなどの酸化剤を用いた常温酸化方
法
(3)直接燃焼、触媒燃焼を利用した高温酸化方法(4
)有効な脱臭剤を用いて、悪臭成分を吸着除去する吸着
方法
などが良く使用されているが、各々一長一短がある。2
(1)については、その除去効果(脱臭効果)が充分で
はない。Methods for deodorizing these foul-smelling gases include (1) cleaning and absorption using acids and alkaline solutions; (2) room-temperature oxidation using oxidizing agents such as potassium permanganate, hypochlorites, and ozone; and (3) direct oxidation. High-temperature oxidation method using combustion and catalytic combustion (4)
) Adsorption methods that use effective deodorizers to adsorb and remove malodorous components are often used, but each method has its advantages and disadvantages. 2 Regarding (1), the removal effect (deodorizing effect) is not sufficient.
(2)については、処理後の排ガス中に含まれる酸化剤
(Ch、03など)の除去用に後処理が必要になる。Regarding (2), post-treatment is required to remove the oxidizing agent (Ch, 03, etc.) contained in the exhaust gas after treatment.
(3)については、高温下で行われる為燃費がかさむ。As for (3), fuel consumption increases because it is carried out at high temperatures.
(4)については、脱臭効果は前者に比べて格段に良い
が、吸着容量に制限があるので寿命がくれば取替える必
要がある。又、脱臭剤層を悪臭が通気する際に圧力損失
があり、静圧の高い送風機が必要である0以上二点の理
由でランニング・コストが割高の方法である。Regarding (4), the deodorizing effect is much better than the former, but the adsorption capacity is limited, so it will be necessary to replace it at the end of its life. In addition, there is a pressure loss when the bad odor is vented through the deodorizing agent layer, and a blower with high static pressure is required.For two reasons, the running cost is relatively high.
等の欠点が指摘されている。The following shortcomings have been pointed out.
一方、(4)の有効な脱臭剤を用いる方法において、近
年適当な金属(Fe、 Mn、 Ni+ Coなど)を
担持添着させて吸着容量の増大を計った活性炭も多く報
告されている。(特開昭49−22390号、特開昭5
3−137071号、特開昭53−137089号、特
開昭54−74271号)
(発明が解決しようとする課題)
前述のように、吸着容量を増大する方法は多く報告され
ているが、脱臭剤そのものの圧力損失を低下する方法は
報告されていす、吸着法による脱臭法では静圧の高い送
風機が要求される為に維持管理において電気代を低下さ
せる事ができなかった。又、脱臭剤を充填する充填塔の
形状を工夫し圧力損失を低下する方向、あるいは通気ス
ピードを低くして圧力損失を低下する方向等の脱臭装置
上の工夫がなされているが、これらの場合には充填塔の
断面積が大きくなり、−回に充填する脱臭剤量が増大す
るなどの欠点があった。On the other hand, in the method (4) using an effective deodorizing agent, there have been many reports in recent years of activated carbon in which appropriate metals (Fe, Mn, Ni + Co, etc.) are supported and impregnated to increase the adsorption capacity. (JP-A-49-22390, JP-A-5
3-137071, JP 53-137089, JP 54-74271) (Problem to be solved by the invention) As mentioned above, many methods for increasing adsorption capacity have been reported, but deodorization Methods to reduce the pressure loss of the agent itself have been reported, but deodorizing methods using adsorption methods require a blower with high static pressure, so it has not been possible to reduce electricity costs during maintenance. In addition, improvements have been made to the deodorizing equipment, such as reducing the pressure loss by changing the shape of the packed tower in which the deodorizing agent is packed, or reducing the pressure loss by lowering the ventilation speed. However, there were drawbacks such as the cross-sectional area of the packed column becoming large and the amount of deodorizing agent packed in each column increasing.
〔課題を解決するための手段〕
本発明者らは従来法の上記欠点を考慮し、鋭意研究の結
果、従来から使用されている脱臭剤に貫通孔を設け、脱
臭剤の中心部を中空状にし、−回に充填する脱臭剤量を
増大させる事なく圧力損失、のみ低下出来る脱臭剤が得
られる事を見出した。[Means for Solving the Problems] The present inventors took into consideration the above-mentioned drawbacks of the conventional method and, as a result of intensive research, created a through-hole in the deodorizer that has been used conventionally, and made the central part of the deodorizer hollow. It has been found that a deodorizing agent can be obtained which can reduce pressure loss without increasing the amount of deodorizing agent charged in the first cycle.
第1図は吸着塔内の吸着進行状態を表わす図であり、一
般に吸着は第1図に示すように進行する。図中イは既吸
着帯、口は吸着帯(吸着進行中)、ハは未吸着帯を表し
、Zは充@層高、Zaは吸着帯の長さを表す。FIG. 1 is a diagram showing the progress of adsorption in the adsorption tower, and generally adsorption progresses as shown in FIG. In the figure, A represents the adsorbed zone, the mouth represents the adsorbed zone (in progress of adsorption), C represents the unadsorbed zone, Z represents the full layer height, and Za represents the length of the adsorbed zone.
一方、第2図は脱臭剤の断面図であり、第1図の吸着帯
の部分にある個々の脱臭剤の吸着は第2図の様に進行す
る。図中イは吸着前、口、ハは吸着中、二は吸着完了の
状態を表す。On the other hand, FIG. 2 is a sectional view of the deodorizer, and adsorption of the individual deodorizers in the adsorption zone portion of FIG. 1 proceeds as shown in FIG. In the figure, A indicates the state before adsorption, C indicates the state during adsorption, and 2 indicates the state of completion of adsorption.
吸着反応における律速段階は、内部拡散である事がほと
んどで、同時に脱臭剤の様に内部に細孔を有する多孔質
物質の場合は、内部拡散=細孔拡散となる。In most cases, the rate-determining step in adsorption reactions is internal diffusion, and in the case of porous materials with internal pores, such as deodorizers, internal diffusion = pore diffusion.
本発明の脱臭剤の形状としては円柱、楕円柱、三角柱、
四角柱状など、どの様な形状でも良く又それらを貫通す
る穴の形状もいかなるものでもよく、穴の数も任意に選
定可能である。The shape of the deodorizer of the present invention is a cylinder, an elliptical cylinder, a triangular cylinder,
They may have any shape, such as a rectangular prism, and the holes passing through them may have any shape, and the number of holes can be arbitrarily selected.
今ここに脱臭剤および貫通孔の形状が円柱状である場合
について言及すると、円柱状脱臭剤の断面を中空状にす
る事により内部拡散が早くなり、その結果吸着の反応速
度が増大する。Now, referring to the case where the deodorizer and the through holes are cylindrical in shape, by making the cross section of the cylindrical deodorizer hollow, internal diffusion becomes faster, and as a result, the reaction rate of adsorption increases.
第3図は脱臭剤(貫通孔のあるもの)の断面図であり、
この貫通孔を設けた中空状脱臭剤の吸着は第3図の様に
進行する。イは吸着前、口、ハは吸着中、二は吸着完了
状態を表す。Figure 3 is a cross-sectional view of a deodorizer (one with through holes).
Adsorption of the hollow deodorizer provided with the through-holes proceeds as shown in FIG. 3. A indicates before adsorption, C indicates adsorption, and 2 indicates completion of adsorption.
この結果、第1図に示した吸着モデルのZaの長さが減
少し、同時にZが一定であれば吸着容量の増加となる。As a result, the length of Za in the adsorption model shown in FIG. 1 decreases, and at the same time, if Z is constant, the adsorption capacity increases.
一方、圧力損失については、第4図に示す様に脱臭塔の
見掛上の通気スピード(空塔速度)は同じでも、悪臭ガ
スと脱臭剤との接触時の実スピードが変化する。図中U
は見掛上の通気スピード、ul又はutはそれぞれイ、
貫通孔のない従来の脱臭剤層、口、貫通孔を設けた本発
明の脱臭剤層での通気実スピードを表す。On the other hand, regarding pressure loss, as shown in FIG. 4, even if the apparent ventilation speed (superficial velocity) of the deodorizing tower remains the same, the actual speed at which the malodorous gas and the deodorizing agent come into contact changes. U in the diagram
is the apparent ventilation speed, ul or ut is i, respectively.
It shows the actual ventilation speed in a conventional deodorizing layer without through holes, and in the deodorizing layer of the present invention provided with ports and through holes.
この場合un>uzとなり、圧力損失Δpはu2に比例
するので、本発明の貫通孔を設けた脱臭剤では従来の貫
通孔のない脱臭剤に比べて圧力損失が低下する。In this case, un>uz, and the pressure loss Δp is proportional to u2. Therefore, the deodorizer provided with the through holes of the present invention has a lower pressure loss than the conventional deodorizer without the through holes.
本発明の脱臭剤は硫化水素、メルカプタン、硫化メチル
等のイオウ化合物、アンモニア、ア逅ン類の窒素化合物
、脂肪酸類、アルデヒド類、ケトン類等々広範囲の悪臭
ガス成分除去用の脱臭剤に利用できる。The deodorizing agent of the present invention can be used as a deodorizing agent for removing a wide range of malodorous gas components such as hydrogen sulfide, mercaptans, sulfur compounds such as methyl sulfide, ammonia, nitrogen compounds such as alcohols, fatty acids, aldehydes, ketones, etc. .
従来の脱臭剤は静圧の高い送風機が要求される為に、主
な用途は産業用、又は工業用の脱臭に限られていた。Conventional deodorizers require a blower with high static pressure, so their main use has been limited to industrial use or deodorization for industrial use.
本発明の貫通孔のある脱臭剤の場合は、産業用はもちろ
んの事、静圧の低い低騒音の送風機が利用できるので、
100Vの電源も可能になり、例えば家庭用脱臭器、病
院、事務所等の業務用脱臭器等々新しい分野での発展が
期待できる。In the case of the deodorizer with through-holes of the present invention, not only can it be used for industrial purposes, but also a low-noise blower with low static pressure can be used.
A 100V power supply is now possible, and development in new fields such as household deodorizers and commercial deodorizers for hospitals, offices, etc. can be expected.
以下に実施例、比較例をあげて本発明を説明する。 The present invention will be explained below with reference to Examples and Comparative Examples.
実施例 1
200メツシユ以下の粉末活性炭600g、クールピッ
チ120gを充分に混練し、貫通孔のある形状に押出し
成形する。120 ’Cで1時間乾燥後、常法に従い粒
状活性炭を得る。Example 1 600 g of powdered activated carbon of 200 mesh or less and 120 g of cool pitch are thoroughly kneaded and extruded into a shape with through holes. After drying at 120'C for 1 hour, granular activated carbon is obtained according to a conventional method.
得られた貫通孔のある活性炭100gを、5%の硫酸水
溶液200gに2時間浸漬させ、乾燥後硫酸添着炭を得
る。100 g of the obtained activated carbon with through holes is immersed in 200 g of a 5% sulfuric acid aqueous solution for 2 hours, and after drying, sulfuric acid impregnated carbon is obtained.
本面は外径6′″1φ、内径1′″8φ、長さ10″″
′Lの円柱状脱臭剤である。The main surface has an outer diameter of 6'''1φ, an inner diameter of 1'''8φ, and a length of 10''.
'L cylindrical deodorizer.
比較例 1
実施例1と同様に混練した活性炭を円柱状に押出し或°
形する。その後は、実施例1と同様な処理を施し、円柱
状の硫酸添着炭を得る。Comparative Example 1 Activated carbon kneaded in the same manner as in Example 1 was extruded into a cylindrical shape.
Shape. Thereafter, the same treatment as in Example 1 is performed to obtain cylindrical sulfuric acid-impregnated carbon.
本面の大きさは外径61φ、長さは10”Lである。The main surface has an outer diameter of 61φ and a length of 10”L.
実施例1、比較例1で得られた各々の硫酸添着炭をカラ
ムにZ=35cmの高さに充填し、空間スピードL V
=0.3 ”/−、NH3fi度100 ppmで吸
着テストを行い、出口濃度1 ppmまでの破過吸着量
、吸着帯の長さZa、圧力損失を測定し、結果を第1表
に示す。Each of the sulfuric acid-impregnated carbons obtained in Example 1 and Comparative Example 1 was packed in a column to a height of Z = 35 cm, and the space speed L V
= 0.3''/-, an adsorption test was conducted at NH3fi degree of 100 ppm, and the breakthrough adsorption amount up to the outlet concentration of 1 ppm, the adsorption zone length Za, and the pressure drop were measured. The results are shown in Table 1.
第、1表
実施例 2
200メツシユ以下の活性炭600g、200メツシユ
以下の天然ゼオライト300gを良く混合する。次に5
%のカルボキシメチルセルロース溶液400gに対して
5nC125gを良く溶解させ、上記混合物と充分混練
し、実施例1で使用した押出し機を用いて貫通孔のある
形状に押出し成形した後、120 ’Cで1時間乾燥し
、脱臭剤を得た。Table 1, Example 2 600 g of activated carbon of 200 mesh or less and 300 g of natural zeolite of 200 mesh or less are thoroughly mixed. Next 5
% carboxymethylcellulose solution, thoroughly kneaded with the above mixture, extruded into a shape with through holes using the extruder used in Example 1, and then heated at 120'C for 1 hour. It was dried to obtain a deodorizer.
本面の大きさは外径6′″1φ、内径2″′φ、長さは
10”Lとした。The size of the main surface was an outer diameter of 6'''1φ, an inner diameter of 2'''φ, and a length of 10''L.
比較例 2
実施例2と同様に混練した脱臭剤スラリーを円柱状に押
出し、実施例2と同様に乾燥後脱臭剤を得た。Comparative Example 2 A deodorizing agent slurry kneaded in the same manner as in Example 2 was extruded into a cylindrical shape, and a deodorizing agent was obtained after drying in the same manner as in Example 2.
本面の大きさは外径6′″−φ、長さは10”Lとした
。The size of the main surface was an outer diameter of 6'''-φ and a length of 10''L.
実施例2、比較例2で得られた脱臭剤をカラムにZ=3
5cmの高さに充填し、LV=0.3′I八、)1.s
iJ度11000ppで吸着テストヲ行イ、出口濃度
1 ppmまでの破過吸着量、Za、圧力損失を測定し
、結果を第2表に示す。The deodorizers obtained in Example 2 and Comparative Example 2 were placed in the column at Z=3.
Fill to a height of 5 cm, LV=0.3'I8,)1. s
An adsorption test was carried out at an iJ degree of 11,000 ppm, and the breakthrough adsorption amount, Za, and pressure loss up to an outlet concentration of 1 ppm were measured, and the results are shown in Table 2.
第2表
実施例 3
200メツシユ以下の活性炭600 g、タールピンチ
120gを充分混練し、貫通孔のある形状に押出し成形
する。その後、120°Cで1時間乾燥後常法に従い粒
状活性炭を得る。Table 2 Example 3 600 g of activated carbon of 200 mesh or less and 120 g of tar pinch are thoroughly kneaded and extruded into a shape with through holes. Thereafter, after drying at 120°C for 1 hour, granular activated carbon is obtained according to a conventional method.
得られた貫通孔のある形状の活性炭100gを2%のN
a0)l液200gに2時間浸漬させ、その後乾燥し、
苛性ソーダ添着炭を得た。100g of the obtained activated carbon with through-holes was mixed with 2% N.
a0) Soaked in 200g of liquid for 2 hours, then dried,
Caustic soda impregnated charcoal was obtained.
本面の、大きさは外径4 +″+*φ、内径1′″1φ
、長さは8”Lとした。The size of the main surface is outer diameter 4 +''+*φ, inner diameter 1'''1φ
, the length was 8"L.
比較例 3
実施例3と同様に混練した活性炭を円柱状に押出し、そ
の後は実施例3と同じ処理を施し、円柱状の苛性ソーダ
添着炭を得た。Comparative Example 3 Activated carbon kneaded in the same manner as in Example 3 was extruded into a cylindrical shape, and then subjected to the same treatment as in Example 3 to obtain cylindrical caustic soda-impregnated carbon.
本面の大きさは外径4−φ、長さは8″″′Lとした。The size of this surface was an outer diameter of 4-φ and a length of 8″″L.
実施例3、比較例3で得られた苛性ソーダ添着炭をカラ
ムにZ=35cmの高さに充填し、LV=0.3 ”/
、、 CHjCOOH1度1100pp”i’吸着テス
トを行い、出口濃度1 ppmまでの破過吸着量、Za
、圧力損失を測定し、結果を第3表に示した。The caustic soda-impregnated carbon obtained in Example 3 and Comparative Example 3 was packed in a column to a height of Z = 35 cm, and LV = 0.3''/
,, CHjCOOH 1 degree 1100pp"i' adsorption test was conducted, and the breakthrough adsorption amount up to the outlet concentration of 1 ppm, Za
, the pressure drop was measured and the results are shown in Table 3.
第
3
表
実施例1〜3、比較例1〜3のテスト結果より本発明の
貫通孔のある脱臭剤は従来の円柱状脱臭剤に比べて、吸
着量、Za、圧力損失の点において優れた効果を発揮し
ている。Table 3 From the test results of Examples 1 to 3 and Comparative Examples 1 to 3, the deodorizer with through holes of the present invention was superior to the conventional cylindrical deodorizer in terms of adsorption amount, Za, and pressure loss. It is proving effective.
通常、吸着方法を用いる脱臭法では、悪臭ガス成分が多
種類の複合ガスである為に、数種類の脱臭剤を組合わせ
て使用する。(3〜4層)本発明の脱臭剤を用いると、
1層当たりの脱臭剤層がコンパクトになり、又3〜4層
合計の圧力損失はかなり低減する。その結果、従来の脱
臭剤を充填した脱臭装置に比較すると、建設費、維持管
理費ともに大幅に低減するものである。Usually, in a deodorizing method using an adsorption method, a combination of several types of deodorizing agents is used because the malodorous gas component is a composite gas of many types. (3 to 4 layers) When using the deodorizer of the present invention,
The deodorizer layer per layer becomes compact, and the total pressure loss of 3 to 4 layers is considerably reduced. As a result, compared to conventional deodorizing equipment filled with deodorizing agents, construction costs and maintenance costs are significantly reduced.
第1図は吸着塔内の吸着進行状態を表す図であり、図中
イは既吸着帯、口は吸着帯(吸着進行中)、ハは未吸着
帯、Zは充填層高、Zaは吸着帯の長さを表す。第2図
は第1図の吸着帯の部分にある個々の脱臭剤の断面図で
あり、吸着進行状態を表す。図中イは吸着前、口、ハは
吸着中、4二は吸着完了の状態を表す脱臭剤の断面図で
ある。第3図は吸着帯の部分にある個々の脱臭剤(貫通
孔のあるもの)の断面図であり、吸着進行状態を表す。
図中イは吸着前、口、ハは吸着中、二は吸着完了の状態
を表す脱臭剤の断面図である。
第4図は脱臭剤層での通気スピードを表す図であり、イ
は従来の脱臭剤層、口は貫通孔のある脱臭剤層での通気
スピードを表す図であり、図中Uは見掛上の通気スピー
ド、ul又はu2はそれぞれ48貫通孔のない従来の脱
臭剤層、又は口0貫通孔を設けた本発明の脱臭剤層口で
の通気実スピードを表す。Figure 1 is a diagram showing the progress of adsorption in the adsorption tower. In the figure, A is the adsorbed zone, the opening is the adsorbed zone (adsorption is in progress), C is the unadsorbed zone, Z is the height of the packed bed, and Za is the adsorbed zone. Represents the length of the obi. FIG. 2 is a cross-sectional view of each deodorizer in the adsorption zone portion of FIG. 1, showing the progress of adsorption. In the figure, A is a cross-sectional view of the deodorizer before adsorption, C is during adsorption, and No. 42 is a sectional view of the deodorizer after adsorption is completed. FIG. 3 is a cross-sectional view of each deodorizer (with through holes) in the adsorption zone, showing the progress of adsorption. In the figure, A is a cross-sectional view of the deodorizer before adsorption, C is during adsorption, and D is the state after adsorption is completed. Figure 4 is a diagram showing the ventilation speed in the deodorizer layer, where A is the conventional deodorizer layer, the opening is the diagram showing the ventilation speed in the deodorizer layer with through holes, and U in the diagram is the apparent The above ventilation speed, ul or u2, respectively represents the actual ventilation speed at the opening of the conventional deodorizing layer without 48 through holes or the deodorizing layer of the present invention with 0 through holes.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1174758A JPH0338247A (en) | 1989-07-06 | 1989-07-06 | Deodorant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1174758A JPH0338247A (en) | 1989-07-06 | 1989-07-06 | Deodorant |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0338247A true JPH0338247A (en) | 1991-02-19 |
Family
ID=15984165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1174758A Pending JPH0338247A (en) | 1989-07-06 | 1989-07-06 | Deodorant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0338247A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03163018A (en) * | 1990-11-20 | 1991-07-15 | Takeda Chem Ind Ltd | Agent and method for stabilizing drug solid composition |
EP0514008A1 (en) | 1991-04-19 | 1992-11-19 | Takeda Chemical Industries, Ltd. | Pharmaceutical preparations based on gastrointestinal mucosa-adherent matrixes or coatings |
JP2005052785A (en) * | 2003-08-07 | 2005-03-03 | Nippon Kasei Kk | Deodorant for treating odor and deodorization apparatus consisting of deodorant for treating odor |
JP2017075068A (en) * | 2015-10-14 | 2017-04-20 | 大阪ガスケミカル株式会社 | Active carbon |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5245750B2 (en) * | 1971-11-26 | 1977-11-18 | ||
JPS56100620A (en) * | 1979-09-20 | 1981-08-12 | Mitsubishi Heavy Ind Ltd | Desulfurization method of exhaust gas |
JPS60168536A (en) * | 1983-12-29 | 1985-09-02 | Shinagawa Refract Co Ltd | Molded adsorbent and its preparation |
JPS62201642A (en) * | 1986-02-27 | 1987-09-05 | Keinosuke Isono | Carrier for adsorptive substance and its production |
-
1989
- 1989-07-06 JP JP1174758A patent/JPH0338247A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5245750B2 (en) * | 1971-11-26 | 1977-11-18 | ||
JPS56100620A (en) * | 1979-09-20 | 1981-08-12 | Mitsubishi Heavy Ind Ltd | Desulfurization method of exhaust gas |
JPS60168536A (en) * | 1983-12-29 | 1985-09-02 | Shinagawa Refract Co Ltd | Molded adsorbent and its preparation |
JPS62201642A (en) * | 1986-02-27 | 1987-09-05 | Keinosuke Isono | Carrier for adsorptive substance and its production |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03163018A (en) * | 1990-11-20 | 1991-07-15 | Takeda Chem Ind Ltd | Agent and method for stabilizing drug solid composition |
JPH0825905B2 (en) * | 1990-11-20 | 1996-03-13 | 武田薬品工業株式会社 | Stabilizing agent for pharmaceutical solid composition and stabilizing method |
EP0514008A1 (en) | 1991-04-19 | 1992-11-19 | Takeda Chemical Industries, Ltd. | Pharmaceutical preparations based on gastrointestinal mucosa-adherent matrixes or coatings |
JP2005052785A (en) * | 2003-08-07 | 2005-03-03 | Nippon Kasei Kk | Deodorant for treating odor and deodorization apparatus consisting of deodorant for treating odor |
JP2017075068A (en) * | 2015-10-14 | 2017-04-20 | 大阪ガスケミカル株式会社 | Active carbon |
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