JPH03143525A - Method for controlling discharge of solvent into atmosphere - Google Patents
Method for controlling discharge of solvent into atmosphereInfo
- Publication number
- JPH03143525A JPH03143525A JP1279370A JP27937089A JPH03143525A JP H03143525 A JPH03143525 A JP H03143525A JP 1279370 A JP1279370 A JP 1279370A JP 27937089 A JP27937089 A JP 27937089A JP H03143525 A JPH03143525 A JP H03143525A
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- water
- liquid
- organic liquid
- paint
- 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
- 239000002904 solvent Substances 0.000 title claims abstract description 72
- 239000012298 atmosphere Substances 0.000 title claims abstract description 4
- 238000000034 method Methods 0.000 title claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 49
- 239000000203 mixture Substances 0.000 claims abstract description 21
- 239000003595 mist Substances 0.000 claims abstract description 17
- 230000005587 bubbling Effects 0.000 claims abstract description 11
- 239000007788 liquid Substances 0.000 claims description 62
- 239000003973 paint Substances 0.000 claims description 46
- 238000010521 absorption reaction Methods 0.000 claims description 28
- 238000009835 boiling Methods 0.000 claims description 17
- -1 ester compound Chemical class 0.000 claims description 15
- 239000003799 water insoluble solvent Substances 0.000 claims description 13
- 238000004821 distillation Methods 0.000 claims description 9
- 229940057995 liquid paraffin Drugs 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 6
- 239000003849 aromatic solvent Substances 0.000 claims description 6
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 5
- 238000007592 spray painting technique Methods 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000003367 polycyclic group Chemical group 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 abstract description 9
- 238000000926 separation method Methods 0.000 abstract description 5
- 238000005507 spraying Methods 0.000 abstract description 3
- 239000011248 coating agent Substances 0.000 abstract 3
- 238000000576 coating method Methods 0.000 abstract 3
- 239000007789 gas Substances 0.000 description 21
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
- 238000007664 blowing Methods 0.000 description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000010422 painting Methods 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 230000002745 absorbent Effects 0.000 description 4
- 239000002250 absorbent Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000003021 water soluble solvent Substances 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 235000005956 Cosmos caudatus Nutrition 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 238000003915 air pollution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000002272 engine oil additive Substances 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- QMYGFTJCQFEDST-UHFFFAOYSA-N 3-methoxybutyl acetate Chemical compound COC(C)CCOC(C)=O QMYGFTJCQFEDST-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Treating Waste Gases (AREA)
- Gas Separation By Absorption (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は水不溶性溶剤の大気排出抑制方法に関する。さ
らに詳しくは、とくに芳香族系溶剤および(または)エ
ステル化合物系溶剤を主体とする溶剤の大気排出抑制方
法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for suppressing atmospheric emissions of water-insoluble solvents. More specifically, the present invention particularly relates to a method for suppressing atmospheric emissions of solvents mainly consisting of aromatic solvents and/or ester compound solvents.
[従来の技術]
溶剤ガスの発生源は多数あるが、たとえば車輌の吹付塗
装工程、焼付乾燥工程などで多量に発生する。[Prior Art] Although there are many sources of solvent gas, a large amount of solvent gas is generated, for example, in the spray painting process, baking drying process, etc. of vehicles.
従来より公害対策として、塗装工程などで発生する溶剤
ガスの大気排出を抑制するために各種の方法が採られて
いる。その一つとして発生した溶剤ガスを何らかの手段
で捕集する方法があるが、捕集効率の向上の点から塗料
の改良を伴うものが多い。Conventionally, various methods have been adopted as pollution countermeasures to suppress atmospheric emissions of solvent gases generated during painting processes and the like. One method is to collect the generated solvent gas by some means, but most of these methods involve improving the paint in order to improve the collection efficiency.
たとえば、塗料として水可溶性塗料、すなわち溶剤が水
可溶性の塗料を用い、発生した溶剤ガスをスクラバー装
置に導き、循環水に吸収させ、塗料ミスト中の溶剤は水
洗ブースの水に吸収させることによって大気汚染防止を
図っている。For example, by using a water-soluble paint, that is, a paint whose solvent is water-soluble, the generated solvent gas is led to a scrubber device and absorbed into circulating water, and the solvent in the paint mist is absorbed into the water in the wash booth, thereby releasing it into the air. Efforts are being made to prevent pollution.
[発明が解決しようとする課題]
しかしながら、水可溶性塗料はその溶剤が特殊であり、
コストが高いという欠点がある。[Problems to be solved by the invention] However, water-soluble paints have special solvents;
It has the disadvantage of high cost.
一方、−殻間な芳香族系溶剤やエステル化合物系溶剤な
どの水不溶性溶剤を溶剤の主成分とする塗料(以下、水
不溶性溶剤塗料という)は低コストであるが、発生した
水不溶性溶剤ガスを高効率、低コストで除去する実用的
方法がないのが現状である。On the other hand, paints whose main component is water-insoluble solvents such as intershell aromatic solvents and ester compound solvents (hereinafter referred to as water-insoluble solvent paints) are low-cost, but they generate water-insoluble solvent gas. At present, there is no practical method to remove them with high efficiency and low cost.
本発明は前記の点に鑑みて、水可溶性塗料なとにくらべ
て安価な水不溶性溶剤塗料を用いるばあいに、水可溶性
塗料のばあいのように発生した溶剤の大気排出を高効率
、低コストで抑制しうる方法を提供せんとするものであ
る。In view of the above points, the present invention provides a highly efficient and low-cost way to reduce atmospheric emissions of the solvent generated in the case of water-soluble paints when using water-insoluble solvent paints, which are cheaper than water-soluble paints. The aim is to provide a method that can suppress this problem.
[課題を解決するための手段]
本発明は、単一または複数種の水不溶性溶剤を主体とす
る溶剤の気体を、比較的蒸気圧が低く、前記溶剤と完全
に混和しうる有機液体または該有機液体と水との混合物
からなる吸収液中にバブリングして吸収させることを特
徴とする溶剤の大気排出抑制方法に関する。[Means for Solving the Problems] The present invention converts a solvent gas mainly consisting of one or more kinds of water-insoluble solvents into an organic liquid having a relatively low vapor pressure and which is completely miscible with the solvent. The present invention relates to a method for suppressing atmospheric emissions of a solvent, which is characterized by bubbling and absorbing a solvent into an absorption liquid consisting of a mixture of an organic liquid and water.
[作用および実施例]
本発明は、トルエン、キシレン、高沸点アルキルベンゼ
ン類、アルキル縮合多環化合物類などの芳香族系溶剤、
ヘプタンなどの脂肪族系溶剤、ブチルアセテート、エチ
ルアセテート、カルピトールアセテートなどのエステル
化合物系溶剤の単独または2種以上の混合物の気体を対
象とするものである。ここで気体とは溶剤の霧状物、さ
らには塗料ミストを含む概念である。[Function and Examples] The present invention uses aromatic solvents such as toluene, xylene, high-boiling alkylbenzenes, and alkyl fused polycyclic compounds;
The target gases are aliphatic solvents such as heptane, and ester compound solvents such as butyl acetate, ethyl acetate, and carpitol acetate, either alone or as a mixture of two or more. Here, the concept of gas includes solvent mist and even paint mist.
塗料ミストとは塗料の霧化された状態をいい、溶剤や顔
料、樹脂からなっている。Paint mist refers to the atomized state of paint, which consists of solvent, pigment, and resin.
前記芳香族系溶剤にはスワゾール■(コスモ石油■製)
、ツルペッツ■(エッソ化学■製)(いずれも高沸点ア
ルキルベンゼンとアルキル縮合多環化合物の混合物)な
ども含まれる。The aromatic solvent is Swasol (manufactured by Cosmo Oil).
, Tsurpets ■ (manufactured by Esso Kagaku ■) (both are mixtures of high-boiling point alkylbenzenes and alkyl condensed polycyclic compounds).
また対象とする溶剤は前記水不溶性溶剤を主体とするも
のであれば、水可溶性溶剤を数容量%〜20容量%程度
含むものであってもよい。水可溶性溶剤としてはプロピ
ルアルコール、ブチルアルコールなどがある。In addition, the target solvent may contain a water-soluble solvent of several vol% to about 20 vol%, as long as it is mainly composed of the above-mentioned water-insoluble solvent. Examples of water-soluble solvents include propyl alcohol and butyl alcohol.
前記のごとき水不溶性溶剤を主体とする溶剤を用いるも
のとしては、たとえば車輌、電気製品などの焼付塗料が
ある。Examples of paints using solvents mainly composed of water-insoluble solvents include baking paints for vehicles, electrical appliances, and the like.
これらの塗料は、キシレン、トルエン、スワゾール、ツ
ルペッツなどの芳香族系溶剤を主体として、ブチルアセ
テート、エチルアセテート、カルピトールアセテート、
あるいはn−ブチルアルコール、ブチルセロソルブなど
の水可溶性溶剤を少量含有するものである。These paints are mainly made of aromatic solvents such as xylene, toluene, Swazol, and Tsurpetz, and also contain butyl acetate, ethyl acetate, carpitol acetate,
Alternatively, it contains a small amount of a water-soluble solvent such as n-butyl alcohol or butyl cellosolve.
1.前記水不溶性溶剤の気体を吸収させる有81液体と
しては、それ自体の気化による大気汚染を防止しかつ溶
剤ガスの吸収をよくするために、比較的蒸気圧が低くか
つ前記水不溶性溶剤と完全に混和しうる有機液体が用い
られる。1. The liquid that absorbs the gas of the water-insoluble solvent has a relatively low vapor pressure and is completely compatible with the water-insoluble solvent in order to prevent air pollution due to its own vaporization and to improve absorption of the solvent gas. Miscible organic liquids are used.
このような有機液体としては、流動パラフィン(このも
のはナフテン系炭化水素類を主体とする)、炭素数lX
l0〜3X102個程度の脂肪族炭素水素類、および高
沸点のアルキルベンゼンやアルキルナフタレンなどのア
ルキル縮合多環化合物の単独もしくは混合物などがあげ
られる。これら有機液体は吸収する溶剤の組成を考慮し
て適宜選択され、また溶剤の組成によっては2種以上を
混合して用いるのが捕集効率の点から好ましいばあいも
ある。Such organic liquids include liquid paraffin (which mainly consists of naphthenic hydrocarbons), carbon number lX
Examples include aliphatic hydrocarbons having about 10 to 3×10 2 carbon atoms, and alkyl condensed polycyclic compounds such as high-boiling point alkylbenzenes and alkylnaphthalenes alone or in mixtures. These organic liquids are appropriately selected in consideration of the composition of the solvent to be absorbed, and depending on the composition of the solvent, it may be preferable to use a mixture of two or more in terms of collection efficiency.
流動パラフィンは沸点が300〜400 ’Cと高く、
蒸気圧が常温でほとんどゼロのものである。Liquid paraffin has a high boiling point of 300-400'C.
Its vapor pressure is almost zero at room temperature.
、炭素数lXl0〜3X102個程度の脂肪族炭化水素
類は蒸気圧が常温ではほとんどゼロに近く、250℃で
5〜20maHg程度のものである。具体例としてはエ
ンジンオイル、パラフィン系エンジンオイル添加剤など
があげられる。パラフィン系エンジンオイル添加剤とし
てはエチレンとα−オレフィンの共重合オリゴマー ポ
リブテン、ポリ −α−オレフィンなどがあり、具体的
にはたとえばルーカント■[三菱石油■製、式:%式%
(ここでRは炭素数1〜5程度のアルキル基、X、)’
、、I)はそれぞれ整数である)で表わされる数平均分
子fA 700〜3800のエチレン−α−オレフィン
共重合オリゴマー]などがあげられる。The vapor pressure of aliphatic hydrocarbons having about 1X10 to 3X102 carbon atoms is almost zero at room temperature, and about 5 to 20 maHg at 250°C. Specific examples include engine oil and paraffin engine oil additives. Examples of paraffin-based engine oil additives include copolymerized oligomers of ethylene and α-olefin, polybutene, and poly-α-olefin. is an alkyl group having about 1 to 5 carbon atoms, X, )'
, , I) are integers, respectively), and the number average molecular fA is 700 to 3,800.
高沸点アルキルベンゼンおよびアルキル縮合多環化合物
(以下、高沸点アルキル芳香族化合物という)としては
沸点が150〜270℃程度のものが用いられる。高沸
点のものは単独で用いると常温では固体のものもあり、
そのばあいは他の溶剤に溶解して用いる。高沸点アルキ
ル芳香、族化合物の具体例としてはたとえば前記のスワ
ゾール、ツルペッツなどがあげられる。As the high boiling point alkylbenzene and alkyl condensed polycyclic compound (hereinafter referred to as high boiling point alkyl aromatic compound), those having a boiling point of about 150 to 270°C are used. Some high-boiling point substances are solid at room temperature when used alone;
In that case, it is used after being dissolved in another solvent. Specific examples of high boiling point alkyl aromatic compounds include the above-mentioned Swazol and Tsurpetz.
高粘度(たとえば10cSt以上)の流動パラフィンを
水と混合しないで用いるばあいは溶剤を吸収しない初期
段階では高粘度の故にバブリングが良好に行なえないば
あいがある。このばあいは高沸点アルキル芳香族化合物
と併用するとよい。その際流動パラフィンと高沸点アル
キル芳香族化合物との混合比は100:3〜20(容量
比)の範囲が好ましい。高沸点アルキル芳香族化合物の
割合が前記範囲より少ないと、粘性が高くバブリングが
困難である。低粘度の流動パラフィンを用いるばあいは
低粘度化のために高沸点アルキル芳香族化合物を掛川す
る必要はとくにない。If liquid paraffin having a high viscosity (for example, 10 cSt or more) is used without being mixed with water, bubbling may not be carried out well due to the high viscosity in the initial stage when the solvent is not absorbed. In this case, it is preferable to use it in combination with a high boiling point alkyl aromatic compound. In this case, the mixing ratio of liquid paraffin and high-boiling alkyl aromatic compound is preferably in the range of 100:3 to 20 (volume ratio). If the proportion of the high boiling point alkyl aromatic compound is less than the above range, the viscosity will be high and bubbling will be difficult. When using low viscosity liquid paraffin, there is no particular need to add a high boiling point alkyl aromatic compound to lower the viscosity.
前記吸収用有機液体はそれだけで単独使用してもよいが
、水と混合して用いてもよい。水を混合使用すると発火
などの危険性が低減される。The organic liquid for absorption may be used alone, or may be used in combination with water. Mixing with water reduces the risk of ignition.
また溶剤の気体を吸収用有機液体中にバブリングさせる
ばあい既存設備を利用しようとすると設備的観点から吸
収用有機液体の液量はある程度以上が必要とされ、また
前記吸収用有機液体は高価であるため、水を増量材とし
て用いるばあいもある。さらに水不溶性溶剤塗料のばあ
いは、溶剤に水可溶性溶剤も含まれているため、水を併
用すると捕集効率が向上する。Furthermore, in the case of bubbling the solvent gas into the absorbent organic liquid, if existing equipment is used, the amount of the absorbent organic liquid must exceed a certain level from the equipment point of view, and the absorbent organic liquid is expensive. Therefore, water is sometimes used as a bulking agent. Furthermore, in the case of a water-insoluble solvent paint, since the solvent also contains a water-soluble solvent, the collection efficiency is improved when water is used in combination.
水を併用するばあい、有機液体に対する水の使用量はそ
れほど限定的ではない。有機液体の比率が小さいばあい
は、捕集した溶剤を除くための蒸留の頻度は増加するが
、捕集効率の点からは吸収装置の段数を増加すればよい
。また有機液体の比率が大きいばあいは蒸溜の頻度が少
なくなり、吸収装置の段数を少なくできる。水を併用す
るばあい、有機液体100容量部に対して水80〜20
00容量部の比率が通常の用い方である。When water is used in combination, the amount of water used relative to the organic liquid is not so limited. When the proportion of organic liquid is small, the frequency of distillation to remove the collected solvent increases, but from the viewpoint of collection efficiency it is sufficient to increase the number of stages of the absorption device. In addition, when the proportion of organic liquid is large, the frequency of distillation is reduced, and the number of stages of the absorption device can be reduced. When water is used together, 80 to 20 parts of water per 100 parts by volume of organic liquid.
A ratio of 0.00 parts by volume is commonly used.
溶剤の気体を吸収液中にバブリングさせるには、何ら特
別の装置を必要とせず、たとえば任意の槽に吸収液を収
容し、これに吹込管を挿入し、溶剤の気体を吹込管を通
じて吸収液中にバブリングさせればよい。吹込管は多数
の細孔を設けたものでも、あるいは先端の開口にメツシ
ュなどを取付けたものでもよい。吸収槽は直列あるいは
並列に連結して設けてもよい。吸収液として有機液体と
水との混合物を使用するばあいも何ら特別な装置は必要
としない。溶剤の気体をバブリングさせることにより有
機液体と水との混合が行なわれ、エマルジョン状態のも
のかえられ、このものは静置しないかぎリエマルジジン
状態を維持する。エマルジョン状態の混合物は気体状の
溶剤を良好に吸収できる。エマルジョン安定化用界面活
性剤を使用すれば前記エマルジョン状態をさらに安定化
することができる。Bubbling the solvent gas into the absorption liquid does not require any special equipment; for example, store the absorption liquid in an arbitrary tank, insert a blowing pipe into it, and blow the solvent gas into the absorption liquid through the blowing pipe. Just let it bubble inside. The blowing tube may be provided with a large number of pores, or may have a mesh or the like attached to the opening at its tip. The absorption tanks may be connected in series or in parallel. No special equipment is required when a mixture of organic liquid and water is used as the absorption liquid. By bubbling the solvent gas, the organic liquid and water are mixed and converted into an emulsion state, which remains in the reemulzidine state unless left standing. The mixture in emulsion state can absorb gaseous solvents well. The emulsion state can be further stabilized by using an emulsion stabilizing surfactant.
溶剤を吸収した吸収液の後処理としても各種方法が採用
されるが、通常は次のような方法で行なう。Although various methods are employed for post-treatment of the absorbent that has absorbed the solvent, the following method is usually used.
有機液体の単独使用のばあいは、そのまま蒸留装置に導
き常圧または減圧下で蒸留を行ない、溶剤を留去し、残
留した有機液体を吸収槽に戻す方法と、前記蒸溜の際に
有機液体も留去する方法が用いられる。留去した溶剤は
所望により精製して再使用する。When using an organic liquid alone, there are two methods. A method is also used in which evaporation is also distilled off. The distilled off solvent can be purified and reused if desired.
吸収液として有機液体と水との混合物を使用するばあい
は、分離槽に導き、要すれば分離のためにエマルジョン
破壊用界面活性剤を添加し、有機液体層と水層とに分離
し、有機液体層を前記と同様に蒸留に付せばよい。また
水から分離せずに水と一緒に蒸留に付し、留去後に水と
有機液体を分離してもよい。When a mixture of organic liquid and water is used as the absorption liquid, it is introduced into a separation tank, and if necessary, a surfactant for breaking the emulsion is added for separation to separate the organic liquid layer and the water layer. The organic liquid layer may be subjected to distillation in the same manner as described above. Alternatively, the organic liquid may be subjected to distillation together with water without being separated from the water, and after distillation, the water and the organic liquid may be separated.
有機液体単独使用のばあいも、洗浄などを目的として水
と混合し、前記有機液体と水との併用のばあいと同様に
処理してもよい。When an organic liquid is used alone, it may be mixed with water for the purpose of cleaning, etc., and treated in the same manner as when the organic liquid and water are used together.
前記において溶剤の回収と有機液体のリサイクルを連続
的に行なうには、有機液体単独使用のばあいは、たとえ
ば溶剤を吸収した有機液体の一部を連続的に蒸留装置に
導き、抜き出した有機液体の分量だけフレッシュな有機
液体(蒸留装置からのもの)を補充して吸収槽に戻すな
どの方法が適宜採られる。有機液体と水との混合、物を
用いるばあいは、たとえば分離槽で分離された有機液体
の一部を連続的に抜き出して蒸留装置に導き、抜き出し
た有機液体の分量だけのフレッシュな有機液体を補充し
、水層と混合して吸収槽に戻すなどの方法が適宜採られ
る。In order to continuously recover the solvent and recycle the organic liquid in the above process, if only the organic liquid is used, for example, a part of the organic liquid that has absorbed the solvent is continuously led to a distillation apparatus, and the extracted organic liquid is An appropriate method may be adopted, such as replenishing fresh organic liquid (from the distillation apparatus) in an amount equal to the amount of the liquid and returning it to the absorption tank. When mixing an organic liquid with water, for example, a part of the organic liquid separated in a separation tank is continuously extracted and introduced into a distillation device, and a fresh organic liquid corresponding to the amount of the extracted organic liquid is produced. Methods such as replenishing the water layer, mixing it with the water layer, and returning it to the absorption tank may be adopted as appropriate.
塗装時に発生した気化溶剤は一般に塗料樹脂成分を含有
するミストを同伴する。The vaporized solvent generated during painting generally accompanies a mist containing paint resin components.
かかるミストを同伴する溶剤気体を直接吸収槽に導入す
ると塗料樹脂成分が蓄積して回収操作が頻雑になる。そ
こで本発明では予め塗料ミストを可及的に除去したのち
吸収槽に導入するのが好ましい。塗料ミストを予め除去
するには、ウォーターカーテン、スクラバー装置などで
水と気液接触させる方法などが適宜採用できる。If the solvent gas accompanied by such mist is directly introduced into the absorption tank, paint resin components will accumulate and recovery operations will become more frequent. Therefore, in the present invention, it is preferable to remove as much paint mist as possible in advance before introducing it into the absorption tank. In order to remove the paint mist in advance, a method of bringing it into gas-liquid contact with water using a water curtain, a scrubber device, etc. can be appropriately employed.
なお、塗料ミストを予め除去しても長期間運転すると塗
料樹脂成分が徐々に蓄積してくる。Note that even if the paint mist is removed in advance, paint resin components will gradually accumulate during long-term operation.
このばあい、吸収用有機液体が流動パラフィンまたは脂
肪族炭化水素類であると、これらは塗料樹脂成分を溶解
しないため、該樹脂成分がフロック状の沈澱物となり泡
と一緒になって分散している状態となって、遂には有機
液相の流動性がなくなり、バブリングが不可能になる。In this case, if the absorbing organic liquid is liquid paraffin or aliphatic hydrocarbons, these will not dissolve the paint resin components, so the resin components will form floc-like precipitates and disperse together with foam. Eventually, the fluidity of the organic liquid phase disappears and bubbling becomes impossible.
また吸収用有機液体が高沸点アルキル芳香族化合物であ
るばあいは、塗料樹脂成分を溶解するが、現象の解明に
は至っていないけれども処理量が多くなると、液を目が
ヨーグルト状となって、流動性がなくなり、やはりバブ
リングか不可能になる。In addition, if the absorbing organic liquid is a high boiling point alkyl aromatic compound, it will dissolve the paint resin component, but although the phenomenon has not yet been elucidated, as the amount of treatment increases, the liquid becomes yogurt-like. There will be no liquidity, and it will either bubble or become impossible.
本発明においては、このような状態のときに、界面活性
剤を加えると、フロック状またはヨーグルト状の塗料樹
脂が凝集し、有機液相の流動性が出て、バブリングが可
能になることが見出された。In the present invention, it has been found that when a surfactant is added in such a state, the floc-like or yoghurt-like paint resin aggregates, the organic liquid phase becomes fluid, and bubbling becomes possible. Served.
用いる界面活性剤の種類は、系が複雑であるから、トラ
イアンドエラーで決定するのがよいが、たとえば家庭用
液体洗剤(たとえばママレモン■(ライオン■製)など
)などで充分な効果かえられる。The type of surfactant to be used is best determined by trial and error since the system is complex, but a household liquid detergent (for example, Mama Lemon ■ (manufactured by Lion ■), etc.) can be used to achieve sufficient effects.
つぎに実施例をあげて本発明を説明する。Next, the present invention will be explained with reference to Examples.
下記実施例では、第1図に示す小型塗装ブース、小型ス
クラバー装置および小型吸収槽を備えた実験装置を使用
して水不溶性溶剤塗料の吹付塗装時に発生した溶剤を捕
集する実験を行なった。In the following example, an experiment was conducted to collect the solvent generated during spray painting of a water-insoluble solvent paint using an experimental device equipped with a small painting booth, a small scrubber device, and a small absorption tank shown in FIG.
第1図において、(財)は小型塗装ブース(巾350m
+ex長さ 650mmX高さ70mm、容積0.01
8m′)、■は該ブースに併設されているスクラバー装
置、(40)は吸収槽、(50〉は排気管である。In Figure 1, the Foundation has a small painting booth (width 350m).
+ex length 650mm x height 70mm, volume 0.01
8m'), (2) is a scrubber device attached to the booth, (40) is an absorption tank, and (50> is an exhaust pipe).
ブース□とスクラバー装置(4)との境にはウォーター
カーテン01)(給水量18.9N /分)が設けられ
ている。A water curtain 01) (water supply amount: 18.9 N/min) is provided between the booth □ and the scrubber device (4).
ブース□□□での吹付は塗装時に発生した溶剤ガス、塗
料ミストはウォーターカーテン01)を通して塗料ミス
トの大部分を除去されたのちスクラバー装置−〇にその
下部から導入され、シャワー装ff1(21)からスプ
レーされた水と気液接触させられ塗料ミストがほぼ安全
に抽果される。塗料ミストを捕集した水はブース(財)
の下部に集められウォーターカーテン水と混合される。In the spraying at booth □□□, most of the paint mist is removed through the solvent gas generated during painting and the water curtain 01), and then introduced into the scrubber device -〇 from the bottom, and then into the shower equipment ff1 (21). The paint mist is almost safely extracted by contact with the water sprayed from the paint. The water that collected the paint mist is collected by Booth (foundation)
The water is collected at the bottom of the water curtain and mixed with water.
該混合物は固形分分離槽02)に送られ、固形分を分離
された水層は貯水タンク税に送られ、そこからウォータ
ーカーテン(II)およびシャワー装置(21)に供給
される。The mixture is sent to the solid content separation tank 02), and the water layer from which the solid content has been separated is sent to the water storage tank, from where it is supplied to the water curtain (II) and the shower device (21).
スクラバー装置■はファン(31〉を備えた排気ダクト
■に接続しており、ダクトのは吹込管(32)に接続し
ており、吹込管(32)の先端開口にはメツシュ(33
)が取付けられている。スクラバー装置囚で塗料ミスト
をほぼ安全に除去された溶剤ガスはファン(31)によ
りダクトのを通し、吹込管(32)から吸収槽(40)
中に収容されている吸収液〈41〉中にバブリングされ
る。溶剤ガスを除去された排ガスは排気管(50)から
大気中に排出される。吸収槽(40)としてはドラム缶
(内径570mm 、高さ880am)を用い、吹込管
(32)としては排気ダクトのと同径の内径70■のパ
イプの先端開口に目の開きが0.5〜1.On+mのメ
ツシュを取付けたものを用いた。The scrubber device ■ is connected to an exhaust duct ■ equipped with a fan (31), and the duct is connected to a blowing pipe (32), and the opening at the tip of the blowing pipe (32) is connected to a mesh (33).
) is installed. The solvent gas from which the paint mist has been almost safely removed by the scrubber device is passed through the duct by the fan (31) and from the blowing pipe (32) to the absorption tank (40).
It is bubbled into the absorption liquid <41> contained therein. The exhaust gas from which the solvent gas has been removed is discharged into the atmosphere from the exhaust pipe (50). A drum can (inner diameter 570 mm, height 880 am) is used as the absorption tank (40), and the blow pipe (32) is a pipe with an inner diameter of 70 cm, the same diameter as the exhaust duct, with an opening at the end of the pipe having an opening of 0.5 to 0.5 mm. 1. One with an On+m mesh attached was used.
溶剤濃度は第1図の塗装ブース(′IO)の中央部内で
入口濃度を測定し、排気管(50)の出口部(81で出
口濃度を測定し、これらの値から溶剤の捕集効率を求め
た。The solvent concentration is determined by measuring the inlet concentration in the center of the painting booth ('IO) in Figure 1, and measuring the outlet concentration at the outlet (81) of the exhaust pipe (50). From these values, the solvent collection efficiency can be calculated. I asked for it.
以下の実施例において%は重量%である。また溶剤組成
における各溶剤の割合は塗料全体に対する割合(%)で
ある(以下、同様)。In the following examples, percentages are percentages by weight. Further, the proportion of each solvent in the solvent composition is the proportion (%) to the entire paint (the same applies hereinafter).
実施例1〜3
第1図に示す実験装置で下記塗料の吹付塗装時に発生し
た溶剤の捕集効率を測定した。Examples 1 to 3 Using the experimental apparatus shown in FIG. 1, the collection efficiency of the solvent generated during spray painting of the following paints was measured.
塗料:ホワイト塗装のソリッド系塗料
塗料樹脂ニアミノアルキッド樹脂
固形分量:57%
溶剤組成:キシレン20%、スワゾール15%、3−メ
トキシブチルア
セテート3%、n−ブチルア
ルコール5%
塗料吐m ffi : 10m1 /分または40
m1/分
スクラバー装置■
シャワー段数二6段
吹込管(32)内の風速(風量):
19m/5ec(44yd/分)
吸収液:水27411と下記有機液体9gの混合物実施
例1:白石ソルベント6号■(日本石油■製の炭素数1
6〜21個の脂肪
族炭化水素と高沸点芳香族化合
物の混合物)
:コスモP−Go (コスモ石油■製のの流動パラフィ
ン
実施例3:ソルベッソ200(エッソ化学■製の高沸点
アルキルベンゼンとア
ルキル縮合多環化合物の混合物)
表に示す。Paint: White painted solid paint Paint resin Niamino alkyd resin Solid content: 57% Solvent composition: xylene 20%, Swasol 15%, 3-methoxybutyl acetate 3%, n-butyl alcohol 5% Paint discharge mffi: 10ml /min or 40
m1/min scrubber device ■ Number of shower stages: 26 Wind speed (air volume) in the blowing pipe (32): 19 m/5 ec (44 yd/min) Absorbing liquid: Mixture of water 27411 and the following organic liquid 9 g Example 1: Shiraishi Solvent No. 6 (manufactured by Nippon Oil Corporation, carbon number 1)
Mixture of 6 to 21 aliphatic hydrocarbons and high-boiling aromatic compounds): Cosmo P-Go (liquid paraffin manufactured by Cosmo Oil ■) Example 3: Solvesso 200 (mixture of high-boiling alkylbenzene and alkyl condensation manufactured by Esso Chemical ■) mixture of polycyclic compounds) shown in the table.
[以下余白]
実施例2
結果を第1
実施例4〜6
実施例1〜3で用いた各吸収液に、実施例1〜3で用い
たソリッド塗料から固形分を除いた溶剤のみを9g予め
配合したほかは実施例1〜3と同様にして捕集効率を測
定した。[Leaving space] Example 2 Results are shown in the first example Examples 4 to 6 9 g of the solvent obtained by removing the solid content from the solid paint used in Examples 1 to 3 was added in advance to each absorption liquid used in Examples 1 to 3. The collection efficiency was measured in the same manner as in Examples 1 to 3 except for the blending.
なお、吸収液に塗料溶剤を混入した理由は塗料を吹付け
ていくうちに捕集効率が低下するか否かをチエツクする
実用的なテストを意図したものである。すなわちフレッ
シュな吸収液ではなくランニングにより塗料溶剤が混入
しフレッシュなものからかけはなれた状態での捕集効率
をみるために行なった。The reason why the paint solvent was mixed into the absorption liquid was to conduct a practical test to check whether the collection efficiency decreases as the paint is sprayed. That is, this was carried out to examine the collection efficiency in a state where the paint solvent was mixed in due to running and was far removed from the fresh absorption liquid, rather than the fresh absorption liquid.
結果を第2表に示す。The results are shown in Table 2.
[以下余白]
実施例7〜9
実施例1〜3において各吸収用有機液体を水と混合せず
に単独で用いたほかは実施flt11〜3と同様にして
捕集効率を求めた。なお各有機液体は31J使用した。[Margin below] Examples 7 to 9 The collection efficiency was determined in the same manner as in Examples 11 to 3, except that in Examples 1 to 3, each absorption organic liquid was used alone without being mixed with water. Note that 31 J of each organic liquid was used.
結果を第3表に示す。The results are shown in Table 3.
[以下余白]
[発明の効果]
芳香族系、エステル化合物系などの溶剤の気体、とくに
これら溶剤を主体とする塗料の吹付は塗装時に発生する
溶剤の気体を、低蒸気圧で該溶剤と混和しつる液体中に
バブリングさせることにより、効率よく捕集でき、大気
汚染の防止が図られる。[Blank below] [Effects of the invention] When spraying paints containing aromatic or ester compound-based solvents, especially those based on these solvents, the solvent gas generated during painting can be mixed with the solvent at low vapor pressure. By bubbling it into a liquid, it can be collected efficiently and air pollution can be prevented.
第1図は実施例で使用した溶剤捕集効率測定装置を示す
概略説明図である。
(図面の主要符号)
00) 、塗装ブース
■ニスクラバー装置
(32):吹込管
(40):吸収槽
(41):吸収液FIG. 1 is a schematic explanatory diagram showing a solvent collection efficiency measuring device used in Examples. (Main symbols in the drawing) 00), Paint booth ■ Varnish scrubber device (32): Blowing pipe (40): Absorption tank (41): Absorption liquid
Claims (1)
の気体を、比較的蒸気圧が低く、前記溶剤と完全に混和
しうる有機液体または該液体と水との混合物からなる吸
収液中にバブリングして吸収させることを特徴とする溶
剤の大気排出抑制方法。 2 芳香族系溶剤および(または)エステル化合物系溶
剤を主体とする塗料を吹付け塗装する際に発生した排気
ガスから予め塗料ミストの大部分を除去したものを前記
吸収処理に付す請求項1記載の方法。 3 前記有機液体が、流動パラフィン、炭素数1×10
〜3×10^2個の脂肪族炭化水素類、および高沸点ア
ルキルベンゼンもしくはアルキル縮合多環化合物よりな
る群から選ばれた1種または2種以上の混合物である請
求項1または2記載の方法。 4 溶剤を吸収した有機液体を蒸留に付して溶剤の回収
と該有機液体のリサイクルを行ない、溶剤の大気排出口
濃度の抑制を行なう請求項1、2または3記載の方法。[Scope of Claims] 1. An organic liquid or a mixture of the liquid and water that has a relatively low vapor pressure and is completely miscible with the solvent gas, which is mainly composed of one or more types of water-insoluble solvents. A method for suppressing atmospheric emissions of a solvent, which comprises bubbling and absorbing a solvent into an absorption liquid consisting of: 2. The absorbing treatment is performed after most of the paint mist has been removed in advance from the exhaust gas generated when spray painting a paint mainly composed of an aromatic solvent and/or an ester compound solvent. the method of. 3 The organic liquid is liquid paraffin, carbon number 1 x 10
3. The method according to claim 1, wherein the hydrocarbon is one or a mixture of two or more selected from the group consisting of ~3x10^2 aliphatic hydrocarbons, and high-boiling alkylbenzenes or alkyl fused polycyclic compounds. 4. The method according to claim 1, 2 or 3, wherein the organic liquid that has absorbed the solvent is subjected to distillation to recover the solvent and recycle the organic liquid to suppress the concentration of the solvent at the outlet to the atmosphere.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1279370A JPH03143525A (en) | 1989-10-26 | 1989-10-26 | Method for controlling discharge of solvent into atmosphere |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1279370A JPH03143525A (en) | 1989-10-26 | 1989-10-26 | Method for controlling discharge of solvent into atmosphere |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03143525A true JPH03143525A (en) | 1991-06-19 |
Family
ID=17610209
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1279370A Pending JPH03143525A (en) | 1989-10-26 | 1989-10-26 | Method for controlling discharge of solvent into atmosphere |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03143525A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006289155A (en) * | 2005-04-05 | 2006-10-26 | Honda Motor Co Ltd | Coating facility |
-
1989
- 1989-10-26 JP JP1279370A patent/JPH03143525A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006289155A (en) * | 2005-04-05 | 2006-10-26 | Honda Motor Co Ltd | Coating facility |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4494967A (en) | Process for the removal of impurities from a gas stream containing solvent vapors | |
US4444573A (en) | Hydrotropes and uses thereof | |
CN103157362A (en) | Preparation method of micro-emulsion absorption liquid used for processing organic exhaust gas | |
US4528001A (en) | Method of recovering volatile organic matters | |
CN101844025A (en) | Organic waste gas microemulsion absorbent, and preparation method and use thereof | |
US4303454A (en) | Vapor stripping process | |
CN103007714A (en) | Low-foam organic waste gas absorbent, and preparation method and application thereof | |
CA2140525C (en) | Method for removing and recovering paint overspray in a water wash spray booth | |
JPH02298565A (en) | Method for rendering paint non-tacky by using improved o/w emulsifying agent containing dibasic acid ester | |
JPH03143525A (en) | Method for controlling discharge of solvent into atmosphere | |
US5820748A (en) | Safe removal of gasses, water and solvents from used lubricating oils with vacuum apparatus under mild temperature conditions | |
CN105688637A (en) | Full-atomization absorption waste gas spray device | |
CN109455845A (en) | A kind of vehicle repairing factory exhaust gas waste water cooperative processing method and device | |
US4523932A (en) | Hydrotropes and uses thereof | |
JPH0275321A (en) | Control of evaporation from solvent to air | |
RU2700041C2 (en) | Waste gas processing method containing polycyclic aromatic hydrocarbons | |
KR100321278B1 (en) | A process for recovering volatile organic solvent | |
JP2002045740A (en) | Method and apparatus for removing resinous deposit occurring from coating material | |
JPS6113869B2 (en) | ||
KR100514814B1 (en) | Method For Removing Naphthalene In Coke Gas | |
Lindenberger | NALCOs Hydrocarbon Emission Control Process: A Novel Pollution Control Method | |
JP2017185473A (en) | Method for removing organic solvent in exhaust gas, and remover for organic solvent in exhaust gas and spray agent for removing organic solvent, for use in the same | |
KR20010025359A (en) | Treatment system for volatile organic compounds | |
JPH04100511A (en) | Method for recovering from paint booth flood sheet system | |
CN105396438A (en) | Comprehensive treatment process and device for paining waste gas |