JP4709531B2 - Methods for removing volatile organic substances from new materials - Google Patents
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Description
本発明は、揮発性有機物質を放散し得る新材料からの揮発性有機物質の除去方法に関する。 The present invention relates to a method for removing volatile organic substances from a new material capable of releasing volatile organic substances.
近年、合成樹脂が含浸された木質建材、壁紙等の新材料が住宅や家具、キッチン、洗面台等に利用されつつある。これら新材料は、ホルムアルデヒド(HCHO)、アセトアルデヒド(CH3CHO)、トルエン(C6H5CH3)、キシレン(C6H4(CH3)2)、スチレン(C6H5CH=CH2)、エチルベンゼン(C6H5CH2CH3)、パラジクロロベンゼン(C6H4Cl2)、テトラデカン(CH3(CH2)12CH3)等の揮発性有機物質(VOC)を放散するおそれがある。このため、新築の住宅等においては、これら揮発性有機物質が室内に蓄積され、シックハウス症候群等が引き起こされることが懸念されている。 In recent years, new materials such as wooden building materials and wallpaper impregnated with synthetic resins are being used in houses, furniture, kitchens, washstands, and the like. These new materials are formaldehyde (HCHO), acetaldehyde (CH 3 CHO), toluene (C 6 H 5 CH 3) , xylene (C 6 H 4 (CH 3 ) 2), styrene (C 6 H 5 CH = CH 2 ), Ethylbenzene (C 6 H 5 CH 2 CH 3 ), paradichlorobenzene (C 6 H 4 Cl 2 ), tetradecane (CH 3 (CH 2 ) 12 CH 3 ) and other volatile organic substances (VOC) There is. For this reason, in newly built houses, etc., there is a concern that these volatile organic substances accumulate indoors and cause sick house syndrome and the like.
このため、新築の住宅において、人が居住等する前に室内の温度及び湿度を上げて揮発性有機物質を新材料からなる建材から予め放散させ、室外に排気する方法が提案されている(特許文献1)。この方法によれば、室内の湿度を上げていることから、揮発性有機物質のうち、水溶性物質を建材から放散させ易く、除去し易い。 For this reason, in a newly built house, a method has been proposed in which the temperature and humidity in a room are raised before a person lives, etc., and volatile organic substances are pre-dissipated from building materials made of a new material and exhausted outside the room (patent) Reference 1). According to this method, since the indoor humidity is increased, among the volatile organic substances, the water-soluble substance is easily diffused from the building material and is easily removed.
また、室内の温度を上げつつ湿度を下げて揮発性有機物質を建材から予め放散させ、室外に排気する方法も提案されている(特許文献2)。この方法によれば、室内の湿度を下げていることから、揮発性有機物質のうち、非水溶性物質を建材から放散させ易く、除去し易い。 In addition, a method has been proposed in which the volatile organic substance is preliminarily dissipated from the building material by raising the indoor temperature while lowering the humidity, and exhausted to the outside (Patent Document 2). According to this method, since the indoor humidity is lowered, among the volatile organic substances, the water-insoluble substances can be easily diffused from the building materials and can be easily removed.
なお、これらの際、建材から放散した揮発性有機物質を室内で吸着することも行われ得る。 In these cases, a volatile organic substance diffused from the building material can be adsorbed indoors.
しかし、上記従来の方法では、室内の湿度を上げる方法と室内の湿度を下げる方法とを連続することとしていないため、水溶性物質と非水溶性物質とに分類される揮発性有機物質を新材料から効率良く除去することが困難であった。 However, in the conventional method described above, the method for increasing the indoor humidity and the method for decreasing the indoor humidity are not continued. Therefore, a volatile organic substance classified into a water-soluble substance and a water-insoluble substance is used as a new material. It has been difficult to remove efficiently.
本発明は、上記従来の実情に鑑みてなされたものであって、新材料から揮発性有機物質を効率良く除去することができる方法を提供することを解決すべき課題としている。 This invention is made | formed in view of the said conventional situation, Comprising: It aims at providing the method which can remove a volatile organic substance from a new material efficiently.
本発明の新材料からの揮発性有機物質の除去方法は、水溶性物質及び非水溶性物質から なる揮発性有機物質を放散し得る新材料をチャンバー内に入れ、該チャンバー内を高温状態かつ湿潤状態の第1雰囲気中に保持して該水溶性物質を該チャンバー内に放散する第1工程と、
該第1工程に連続し、該チャンバー内を高温状態かつ乾燥状態の第2雰囲気中に保持し て該非水溶性物質を該チャンバー内に放散する第2工程とを有することを特徴とする。The method for removing a volatile organic substance from a new material according to the present invention comprises placing a new material capable of releasing a volatile organic substance composed of a water-soluble substance and a water-insoluble substance in a chamber, and heating the chamber in a high-temperature and wet state. A first step of maintaining the first atmosphere in a state to dissipate the water-soluble substance into the chamber ;
Successively to the first step, and having a second step of holding the chamber in the second atmosphere hot state and dried state for dissipating water-insoluble substance in the chamber.
本発明の除去方法は、第1工程において、新材料を高温状態かつ湿潤状態の第1雰囲気中に保持する。このため、揮発性有機物質のうちの水溶性物質をその新材料から放散させ、除去することができる。ここで、揮発性有機物質のうちの水溶性物質とは、ホルムアルデヒド、アセトアルデヒド等である。 In the removal method of the present invention, in the first step, the new material is held in a first atmosphere in a high temperature and wet state. For this reason, the water-soluble substance of a volatile organic substance can be diffused from the new material, and can be removed. Here, water-soluble substances among volatile organic substances are formaldehyde, acetaldehyde, and the like.
そして、第2工程において、新材料を高温状態かつ乾燥状態の第2雰囲気中に保持する。このため、揮発性有機物質のうちの非水溶性物質をその新材料から放散させ、除去することができる。ここで、揮発性有機物質のうちの非水溶性物質とは、トルエン、キシレン、スチレン、エチルベンゼン、パラジクロロベンゼン、テトラデカン等である。 And in a 2nd process, a new material is hold | maintained in the 2nd atmosphere of a high temperature state and a dry state. For this reason, the water-insoluble substance of a volatile organic substance can be diffused from the new material, and can be removed. Here, the water-insoluble substances among the volatile organic substances are toluene, xylene, styrene, ethylbenzene, paradichlorobenzene, tetradecane and the like.
特に、本発明の除去方法においては、第2工程を第1工程に連続することとしている。このため、本発明の除去方法によれば、第1工程によって、揮発性有機物質のうちの水溶性物質を放散させ、第2工程によって、放散する通路をその水溶性物質によって塞がれていた非水溶性物質も放散させることができ、これらを除去することができると考えられる。 In particular, in the removal method of the present invention, the second step is continued from the first step. For this reason, according to the removal method of the present invention, the water-soluble substance of the volatile organic substance is diffused by the first step, and the dissipating passage is blocked by the water-soluble substance by the second step. It is believed that water-insoluble materials can also be diffused and removed.
また、本発明の除去方法においては、各工程を高温状態で維持することにしている。これにより、沸点が常温に近いアセトアルデヒドについては、水溶性物質であることにより第1工程で放散した後、第2工程に至る途中でも連続して放散させることができる。 In the removal method of the present invention, each step is maintained at a high temperature. As a result, acetaldehyde having a boiling point close to room temperature can be continuously dissipated even in the middle of reaching the second step after being dissipated in the first step due to being a water-soluble substance.
したがって、本発明の除去方法によれば、新材料から揮発性有機物質を効率良く除去することができる。 Therefore, according to the removal method of the present invention, volatile organic substances can be efficiently removed from the new material.
なお、本発明の除去方法における第1工程と第2工程とを入れ替えた揮発性有機物質の除去方法においては、揮発性有機物質のうちの水溶性物質と揮発性有機物質のうちの非水溶性物質とを除去する順序が本発明の除去方法とは逆になる。この方法によっても、本発明と同様の作用効果を奏することができる。 In addition, in the removal method of the volatile organic substance which replaced the 1st process and the 2nd process in the removal method of this invention, the water-insoluble substance of the volatile organic substance and the water-insoluble substance of the volatile organic substance The order of removing the substances is reversed from the removal method of the present invention. Also by this method, the same effects as those of the present invention can be achieved.
また、発明者の考察によれば、本発明の除去方法は第1工程と第2工程とを連続して交互に繰り返すものであることが好ましい。この場合、水溶性物質と非水溶性物質とが放散するための各々の通路を互いに塞いでいる状態においても、これらを交互に放散させ、除去することができるからである。このため、この方法によれば、新材料中に含まれた揮発性有機物質を更に効率良く除去することができる。 Moreover, according to inventors' consideration, it is preferable that the removal method of this invention repeats a 1st process and a 2nd process alternately alternately. In this case, even in a state where the respective passages for the water-soluble substance and the water-insoluble substance to be diffused are closed, they can be diffused and removed alternately. For this reason, according to this method, the volatile organic substance contained in the new material can be more efficiently removed.
本発明は、新材料をチャンバー内に入れて行なう。これにより、高温状態で湿度を上下させる空間を小さく抑えることができるため、除去時間を短縮できる。また、この場合、空間内の熱や湿気の漏れを防止しやすい。また、この場合、新材料の全面から揮発性有機物質の除去を行なうことができる。これらのことから、新材料から揮発性有機物質をより効率良く除去することができる。また、この場合、放散後の揮発性有機物質を空間外に漏らしにくいことから、作業環境の悪化や周囲の環境汚染を引き起こすこともない。チャンバー内に入れる際、新材料を組付けた後において行うことも可能であるが、組付け前に行なうことが好ましい。The present invention will row the new material put into the chamber. This ensures that it is possible to reduce the space to lower the humidity at a high temperature, it can be shortened removal time. In this case, it is easy to prevent leakage of heat and moisture in the space. In this case, the volatile organic substance can be removed from the entire surface of the new material. For these reasons , volatile organic substances can be more efficiently removed from the new material. Further, in this case, since the volatile organic substance after the diffusion is difficult to leak out of the space, the working environment is not deteriorated and the surrounding environment is not polluted. When and place in the chamber, it is also possible to carry out after the assembling of the new material, it is preferably performed before assembly.
以下、図面を参照しつつ、本発明を具体化した実施例を比較例とともに説明する。 DESCRIPTION OF THE PREFERRED EMBODIMENTS Embodiments embodying the present invention will be described below together with comparative examples with reference to the drawings.
まず、揮発性有機物質を放散し得る新材料として、160mm×160mm×15mmの標準試験片を用意した。この標準試験片は木材のチップを接着剤で固めて平板にしたものを芯にして、その表面と裏面とに化粧紙を接着剤で貼り付けて成形したものである。この標準試験片を容積20Lのチャンバー(有限会社アドテック製)内に入れた。 First, a standard test piece of 160 mm × 160 mm × 15 mm was prepared as a new material capable of diffusing volatile organic substances. This standard test piece is formed by sticking a wood chip with an adhesive into a flat plate and attaching a decorative paper to the front and back surfaces with an adhesive. This standard test piece was placed in a 20 L chamber (manufactured by Adtec Co., Ltd.).
そして、第1工程前において、通常状態における標準試験片からの揮発性有機物質の放散量を確認するため、チャンバー内の雰囲気を温度28°C、湿度50%、換気回数0.5回/hとしてチャンバーを密閉し、この温度と湿度とを24時間保持した。この間のチャンバー内の揮発性有機物質の濃度(μg/m3)を計測した。ここで、揮発性有機物質として計測する対象は、個別に計測したホルムアルデヒド、アセトアルデヒド、トルエン、キシレン、スチレン、エチルベンゼン、パラジクロロベンゼン及びテトラデカン並びに総揮発性有機物質である。なお、総揮発性有機物質は、ホルムアルデヒド等のほか、個別に計測していない揮発性有機物質を含むものである。 Before the first step, in order to confirm the amount of volatile organic substances released from the standard test piece in a normal state, the atmosphere in the chamber is set to a temperature of 28 ° C., a humidity of 50%, and a ventilation frequency of 0.5 times / h. The chamber was sealed and this temperature and humidity were maintained for 24 hours. During this time, the concentration (μg / m 3 ) of the volatile organic substance in the chamber was measured. Here, the objects to be measured as volatile organic substances are individually measured formaldehyde, acetaldehyde, toluene, xylene, styrene, ethylbenzene, paradichlorobenzene, tetradecane, and total volatile organic substances. The total volatile organic substances include formaldehyde and other volatile organic substances not individually measured.
次に、第1工程として、チャンバー内を第1雰囲気としての温度40°C、湿度50%、換気回数0.5回/hである高温状態かつ湿潤状態に24時間保持した。この間のチャンバー内の対象の濃度(μg/m3)を計測した。 Next, as a first step, the inside of the chamber was kept at a high temperature and a wet state of a temperature of 40 ° C. as a first atmosphere, a humidity of 50%, and a ventilation frequency of 0.5 times / h for 24 hours. During this time, the concentration (μg / m 3 ) of the target in the chamber was measured.
続いて、第1工程に連続して第2工程を行った。すなわち、チャンバー内を第2雰囲気としての温度40°C、湿度22%、換気回数0.5回/hである高温状態かつ乾燥状態に24時間保持した。この間のチャンバー内の対象の濃度(μg/m3)を計測した。 Subsequently, the second step was performed continuously to the first step. That is, the inside of the chamber was kept at a high temperature and a dry state for 24 hours as a second atmosphere at a temperature of 40 ° C., a humidity of 22%, and a ventilation rate of 0.5 times / h. During this time, the concentration (μg / m 3 ) of the target in the chamber was measured.
そして、第2工程後において、以上の方法による効果を確認するため、チャンバー内の雰囲気を第1工程前と同様に温度28°C、湿度50%、換気回数0.5回/hの通常状態とし、この温度と湿度とを24時間保持した。この間のチャンバー内の対象の濃度(μg/m3)を計測した。 Then, after the second step, in order to confirm the effect by the above method, the atmosphere in the chamber is the same as before the first step, with the temperature being 28 ° C., the humidity being 50%, and the ventilation frequency being 0.5 times / h. The temperature and humidity were maintained for 24 hours. During this time, the concentration (μg / m 3 ) of the target in the chamber was measured.
これらの結果を表1及び図1〜5に示す。図1はホルムアルデヒドの濃度を示し、図2はアセトアルデヒドの濃度を示し、図3はスチレンの濃度を示し、図4はエチルベンゼンの濃度を示し、図5は総揮発性有機物質の濃度を示す。 These results are shown in Table 1 and FIGS. FIG. 1 shows the concentration of formaldehyde, FIG. 2 shows the concentration of acetaldehyde, FIG. 3 shows the concentration of styrene, FIG. 4 shows the concentration of ethylbenzene, and FIG. 5 shows the concentration of total volatile organic substances.
表1及び図1〜4より、ホルムアルデヒド、アセトアルデヒド、スチレン及びエチルベンゼンは、第1工程前において検出されなかったことがわかる。これにより、これらの対象は、通常状態において、24時間経過しただけではそのほとんどが放散されないと考えられる。 From Table 1 and FIGS. 1-4, it turns out that formaldehyde, acetaldehyde, styrene, and ethylbenzene were not detected before the 1st process. Accordingly, it is considered that most of these objects are not diffused only after 24 hours have passed in the normal state.
また、水溶性物質であるホルムアルデヒド及びアセトアルデヒドは、第1工程と第2工程とにおいて検出されており、特に、第1工程である高温状態かつ湿潤状態において多く検出されたことがわかる。これにより、水溶性物質であるこれらの対象は、第1工程の高温状態かつ湿潤状態において放散された後、第2工程において除去されなかったその残留分が検出されたと考えられる。 Further, it can be seen that formaldehyde and acetaldehyde, which are water-soluble substances, were detected in the first step and the second step, and in particular, they were detected in a high temperature and in a wet state, which are the first step. Accordingly, it is considered that those objects that are water-soluble substances were detected in the residue that was not removed in the second step after being diffused in the high temperature and wet state of the first step.
一方、非水溶性物質であるスチレン及びエチルベンゼンは、第1工程においては検出されず、第2工程において検出されたことがわかる。これにより、非水溶性物質であるこれらの対象は、第1工程である高温状態かつ湿潤状態においてはそのほとんどが放散されず、第2工程である高温状態かつ乾燥状態において放散されていることがわかる。 On the other hand, styrene and ethylbenzene, which are water-insoluble substances, are not detected in the first step, but are detected in the second step. As a result, most of these objects that are water-insoluble substances are not dissipated in the high temperature and wet state of the first step, but are diffused in the high temperature and dry state of the second step. Recognize.
また、ホルムアルデヒド、アセトアルデヒド、スチレン及びエチルベンゼンは、第2工程後において検出されなかったことがわかる。これにより、これらの対象は、第2工程後の排気によって除去されたと考えられる。 It can also be seen that formaldehyde, acetaldehyde, styrene and ethylbenzene were not detected after the second step. Thereby, it is considered that these objects were removed by the exhaust after the second step.
さらに、表1及び図5より、総揮発性有機物質は第1工程前において検出されたことがわかる。これにより、通常状態において、個別に計測したホルムアルデヒド、アセトアルデヒド、トルエン、キシレン、スチレン、エチルベンゼン、パラジクロロベンゼン及びテトラデカン以外の揮発性有機物質が放散されたことがわかる。 Furthermore, it can be seen from Table 1 and FIG. 5 that the total volatile organic substances were detected before the first step. Thereby, it can be seen that volatile organic substances other than formaldehyde, acetaldehyde, toluene, xylene, styrene, ethylbenzene, paradichlorobenzene and tetradecane, which were individually measured, were diffused in a normal state.
また、第1工程において第1工程前より総揮発性有機物質の濃度が高くなり、第2工程において更にこの濃度が増加していることがわかる。これにより、第1工程である高温状態かつ湿潤状態において、揮発性有機物質のうちの水溶性物質が放散され、第2工程である高温状態かつ乾燥状態において、揮発性有機物質のうちの非水溶性物質が放散されたと考えられる。 Further, it can be seen that the concentration of the total volatile organic substance is higher in the first step than before the first step, and this concentration is further increased in the second step. Thereby, the water-soluble substance of the volatile organic substance is diffused in the high temperature state and the wet state as the first step, and the water-insoluble substance of the volatile organic substance in the high temperature state and the dry state as the second step. It is thought that the sexual substance was released.
特に、実施例においては、第2工程を第1工程に連続することとしている。このため、第1工程において、揮発性有機物質のうちの水溶性物質を放散させ、第2工程において、放散する通路をその水溶性物質によって塞がれていた揮発性有機物質のうちの非水溶性物質も放散させ、これらを除去することができたと考えられる。 In particular, in the embodiment, the second step is continued from the first step. For this reason, in the first step, the water-soluble substance of the volatile organic substance is dissipated, and in the second step, the dissipating passage is blocked by the water-soluble substance. It is thought that the active substances were also diffused and removed.
さらに、第2工程後において第1工程前より低い濃度の総揮発性有機物質が検出されたことがわかる。これにより、総揮発性有機物質は、通常状態よりも第1工程と第2工程とによって効率良く放散され、第1工程中の排気、第2工程中の排気及びその後の排気によって除去されたことがわかる。 Furthermore, it can be seen that a lower total volatile organic substance concentration was detected after the second step than before the first step. As a result, the total volatile organic substances are more efficiently dissipated in the first step and the second step than in the normal state, and are removed by the exhaust in the first step, the exhaust in the second step, and the subsequent exhaust. I understand.
なお、表1より、トルエン、キシレン、パラジクロロベンゼン及びテトラデカンは検出されなかったことがわかる。これにより、接着剤にこれらが含まれていないか、または実施例の温度や湿度の条件ではこれらが放散されないと考えられる。 Table 1 shows that toluene, xylene, paradichlorobenzene and tetradecane were not detected. Accordingly, it is considered that these are not contained in the adhesive or are not diffused under the temperature and humidity conditions of the examples.
したがって、実施例の新材料からの揮発性有機物質の除去方法によって、新材料から揮発性有機物質を効率良く除去できることがわかる。 Therefore, it can be seen that the volatile organic substance can be efficiently removed from the new material by the method for removing the volatile organic substance from the new material of the example.
まず、実施例と同様に、新材料としての標準試験片とチャンバーとを用意し、第1工程前と第1工程とにおける処理と計測とを行なった。続いて、第2工程として、第1工程に連続して第1工程と同様の処理と計測とを行なった。つまり、第1工程と第2工程とにおいて、チャンバー内を第1雰囲気としての温度40°C、湿度50%である高温状態かつ湿潤状態に48時間保持し、この間24時間毎に計測を行なった。そして、第2工程後において、実施例の第2工程後と同様の処理と計測とを行なった。 First, in the same manner as in the example, a standard test piece and a chamber as a new material were prepared, and processing and measurement before the first step and in the first step were performed. Subsequently, as the second step, the same processing and measurement as in the first step were performed continuously to the first step. That is, in the first step and the second step, the inside of the chamber was kept in a high temperature and wet state at a temperature of 40 ° C. and a humidity of 50% as a first atmosphere for 48 hours, and measurement was performed every 24 hours during this time. . Then, after the second step, the same processing and measurement as in the second step of the example were performed.
これらの結果を表2に示す。また、これらの結果を実施例の結果と併せて図1〜5に示す。 These results are shown in Table 2. These results are shown in FIGS. 1 to 5 together with the results of the examples.
表1、2及び図3、4より、上記実施例においては、非水溶性物質であるスチレン及びエチルベンゼンは、高温状態かつ乾燥状態の第2工程において検出されている。一方、比較例のように高温状態かつ湿潤状態に曝すと、スチレン及びエチルベンゼンは放散されないことがわかる。 From Tables 1 and 2 and FIGS. 3 and 4, styrene and ethylbenzene, which are water-insoluble substances, were detected in the second step in a high temperature state and a dry state in the above examples. On the other hand, when exposed to a high temperature state and a wet state as in the comparative example, it can be seen that styrene and ethylbenzene are not diffused.
また、表1、2及び図5より、実施例と比較例とを比較すると、比較例の第2工程における総揮発性有機物質の濃度よりも実施例の第2工程における総揮発性有機物質の濃度は高いことがわかる。この差は、比較例の第2工程では揮発性有機物質のうちの非水溶性物質が放散されていないのに対し、実施例の第2工程では揮発性有機物質のうちの非水溶性物質が放散されていることによると考えられる。また、この差は、実施例において第2工程を第1工程に連続することとしていることによって、その第1工程において、揮発性有機物質のうちの水溶性物質を放散させ、その第2工程において、放散する通路をその水溶性物質によって塞がれていた揮発性有機物質のうちの非水溶性物質も放散させたためであるとも考えられる。 Further, from Tables 1 and 2 and FIG. 5, when the example and the comparative example are compared, the total volatile organic substance concentration in the second step of the example is higher than the concentration of the total volatile organic substance in the second step of the comparative example. It can be seen that the concentration is high. This difference is that, in the second step of the comparative example, the water-insoluble substance among the volatile organic substances is not diffused, whereas in the second step of the example, the water-insoluble substance in the volatile organic substance is not diffused. This is thought to be due to the release. In addition, this difference is that the second step is continued from the first step in the embodiment, so that in the first step, the water-soluble substance of the volatile organic substance is diffused, and in the second step, It is also considered that the water-insoluble substance among the volatile organic substances whose passages to be diffused were blocked by the water-soluble substance was also diffused.
したがって、以上のことからも実施例の除去方法によれば、比較例の除去方法によるよりも、揮発性有機物質を効率良く除去できることがわかる。 Therefore, it can be seen from the above that the volatile organic material can be removed more efficiently by the removal method of the embodiment than by the removal method of the comparative example.
以上において、本発明を実施例に即して説明したが、本発明は上記実施例に制限されるものではなく、その趣旨を逸脱しない範囲で適宜変更して適用できることはいうまでもない。 While the present invention has been described with reference to the embodiments, it is needless to say that the present invention is not limited to the above-described embodiments and can be appropriately modified and applied without departing from the spirit thereof.
本発明は、木質建材、壁紙等からの揮発性有機物質の除去方法に利用可能である。 INDUSTRIAL APPLICABILITY The present invention can be used for a method for removing volatile organic substances from wooden building materials, wallpaper, and the like.
Claims (4)
該第1工程に連続し、該チャンバー内を高温状態かつ乾燥状態の第2雰囲気中に保持して該非水溶性物質を該チャンバー内に放散する第2工程とを有することを特徴とする新材料からの揮発性有機物質の除去方法。 A new material capable of dissipating volatile organic substances composed of water-soluble substances and water-insoluble substances is put in a chamber, and the chamber is maintained in a first atmosphere in a high temperature and in a wet state so that the water-soluble substance is contained in the chamber. A first step of diffusing into the chamber;
A second material which is continuous with the first step and has a second step of keeping the inside of the chamber in a high temperature and dry second atmosphere and releasing the water-insoluble substance into the chamber. Of removal of volatile organic substances from water.
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