JPS6034689B2 - Column equipment for gas concentration - Google Patents

Column equipment for gas concentration

Info

Publication number
JPS6034689B2
JPS6034689B2 JP51152452A JP15245276A JPS6034689B2 JP S6034689 B2 JPS6034689 B2 JP S6034689B2 JP 51152452 A JP51152452 A JP 51152452A JP 15245276 A JP15245276 A JP 15245276A JP S6034689 B2 JPS6034689 B2 JP S6034689B2
Authority
JP
Japan
Prior art keywords
gas
column
concentrating column
molecular sieve
desorption
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.)
Expired
Application number
JP51152452A
Other languages
Japanese (ja)
Other versions
JPS5376092A (en
Inventor
欣宏 永石
昭男 吉留
一男 横山
孝 今村
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP51152452A priority Critical patent/JPS6034689B2/en
Publication of JPS5376092A publication Critical patent/JPS5376092A/en
Publication of JPS6034689B2 publication Critical patent/JPS6034689B2/en
Expired legal-status Critical Current

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  • Sampling And Sample Adjustment (AREA)
  • Separation Of Gases By Adsorption (AREA)

Description

【発明の詳細な説明】 本発明は、稀薄気体を橘集濃縮するカラムに関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a column for concentrating diluted gases.

一般に、液体中より不活性気体のバブリングによって溶
存気体を脱気し、その溶存ガスを、ガスクロマトグラフ
等の分析機器を用いて測定しようとする場合、溶存ガス
の脱気状態というのが成分により異なりはするが一気に
脱気されるのではなく連続的に長時間にわたって脱気さ
れていくので単位時間当りの脱気量も少なく、従って、
この脱気した気体を直援分析機器に導びし、ても脱気ガ
スが一成分であれば測定可能であるが多成分になると全
成分が同時、かつ連続的であるためガスクロマトグラフ
内で分離出来ず測定が困難な場合があった。本発明は、
上記のような不都合を鱗消すべく成されたものである。
Generally, when a dissolved gas is degassed from a liquid by bubbling an inert gas and the dissolved gas is measured using an analytical instrument such as a gas chromatograph, the degassed state of the dissolved gas differs depending on the component. Since the gas is not degassed all at once but continuously over a long period of time, the amount of deaeration per unit time is small.
This degassed gas is directly guided to an analytical instrument, and if the degassed gas is a single component, it can be measured, but if the degassed gas contains multiple components, all the components are measured simultaneously and continuously, so it cannot be measured in a gas chromatograph. There were cases where separation was not possible and measurement was difficult. The present invention
This was done to eliminate the above-mentioned inconvenience.

以下本発明の一実施例を詳しく説明する。An embodiment of the present invention will be described in detail below.

即ち、第1図は本発明の一実施例を示し、aは気体吸着
時、bは脱着時を示す。図に於て、1は気体濃縮用カラ
ム(以下単にカラムと略称する)で、内部に吸着剤とし
てモレキュラーシーブ5A2を充填している。
That is, FIG. 1 shows an embodiment of the present invention, in which a shows the state during gas adsorption and b shows the state during desorption. In the figure, reference numeral 1 denotes a gas concentration column (hereinafter simply referred to as column), which is filled with molecular sieve 5A2 as an adsorbent.

3はカラム加熱用ヒータ、4,5は夫々3方弁である。3 is a heater for heating the column, and 4 and 5 are three-way valves.

以上のように構成された装置に於て、先づ、第1図aに
示す如く3方弁4,5をセットし、例えば液体中から脱
気されてきた稀薄な気体をAよりキヤリヤーガスによっ
て三方弁4を介してカラム1内に導入する。カラム1内
に導入された上記気体は吸着剤2により吸着され、キャ
リャーガスは三方弁5を介してBより排出される。上記
液体より脱気された気体が各種成分のガスより成ってい
る場合、吸着剤2に吸着され易い成分のガスがカラム1
の比較的入口側で吸着されるが、吸着剤に吸着されにく
い成分のガスはカラム1の次第に出口側に至って吸着さ
れるような状態となる。さて、気体の吸着が終ると、三
方弁4,5を第1図bのように切換え、Cよりキャリャ
ーガスをカラムー内に導入し三方弁4を介してDへ送り
出す。これにより吸着剤から気体が脱着されてキャリャ
ーガスと共にDより送出されれる。この時、カラム加熱
用ヒータ3を附勢してカラムを加熱すれば、吸着剤から
の気体の脱着がより速やかになる。気体の脱着は速やか
に行なわれるので、希薄な気体であっても濃縮されてD
より送出され、例えば、ガスクロマトグラフ等の分析装
置で充分分析出来るものとなる。
In the apparatus configured as described above, first, the three-way valves 4 and 5 are set as shown in FIG. It is introduced into column 1 via valve 4. The gas introduced into the column 1 is adsorbed by the adsorbent 2, and the carrier gas is discharged from B via the three-way valve 5. When the gas degassed from the liquid is composed of gases of various components, the gases of the components that are easily adsorbed by the adsorbent 2 are in the column 1.
However, gases with components that are difficult to be adsorbed by the adsorbent gradually reach the outlet side of the column 1 and become adsorbed. Now, when the gas adsorption is completed, the three-way valves 4 and 5 are switched as shown in FIG. As a result, gas is desorbed from the adsorbent and sent out from D together with the carrier gas. At this time, if the column heating heater 3 is energized to heat the column, the gas can be desorbed from the adsorbent more quickly. Gas desorption occurs quickly, so even dilute gases are concentrated and D
For example, it can be sufficiently analyzed by an analyzer such as a gas chromatograph.

尚、キャリャーガスを脱着時に吸着時とは逆方向に流す
事により、各種成分のガスの脱着をスムースに行なう。
By flowing the carrier gas during desorption in the opposite direction to that during adsorption, the various component gases can be smoothly desorbed.

以上述べた本発明の濃縮カラムを用いた時の効果を見る
ため、モデル実験として、油の中に、ェタン、エチレン
、フ。ロ/ぐン、フ。ロピレン、アセチレン、n−ブタ
ンを溶けこませ、キヤリャーガスとして、ヘリウムを用
いて脱気し、直接、ガスクロマトグラムに記録させたも
のと、一度気体濃縮用カラムに捕集濃縮させたもののガ
スクロマトグラフを比較した場合、本発明の濃縮用カラ
ムを使用しない場合には、連続的に脱気されている各気
体が満足に分離されずに第2図のようになり、本発明の
気体濃縮用カラムを用いた場合は、第3図のように注射
器で注入したものと同一のクロマトグラムが得られる事
が判った。以上の如く、この発明のカラム装置によれば
、従来のガスクロマトグラフ等による測定で問題になっ
ていた発生源において低濃度の気体や、連続的に測定器
に入って測定が困難であったものを、濃縮して一度に例
えば測定器等に導くことが出来るので、これまで測定の
出来なかった非常に低濃度の気体を測定することが可能
となるものである。
In order to see the effects of using the concentration column of the present invention as described above, a model experiment was conducted in which ethane, ethylene, and fluorine were added to oil. Ro/gun, fu. Comparison of gas chromatographs in which lopylene, acetylene, and n-butane were dissolved, degassed using helium as a carrier gas, and recorded directly on a gas chromatogram, and one in which they were once collected and concentrated in a gas concentration column. In this case, if the concentrating column of the present invention is not used, the continuously degassed gases will not be separated satisfactorily and the result will be as shown in Figure 2. It was found that when the sample was injected with a syringe, the same chromatogram as shown in Figure 3 could be obtained. As described above, according to the column device of the present invention, low concentration gases can be detected at the source, which was a problem when measuring with conventional gas chromatographs, etc., and gases that continuously enter the measuring instrument and are difficult to measure. Since it is possible to condense the gas and introduce it all at once to, for example, a measuring device, it becomes possible to measure gases at extremely low concentrations that could not be measured up to now.

尚、本発明のカラム装置は次のような応用が可能である
The column device of the present invention can be applied in the following ways.

{1) ハンディーエアーサンプラ−で吸収液等に橋集
してし、たものを吸収液の替りに本発明のカラム装置を
使用すれば、移送等に便利である。
{1) If the column device of the present invention is used in place of the absorption liquid by cross-concentrating it with an absorption liquid using a handy air sampler, it will be convenient for transportation.

■ 熱分解発生ガスの測定に際して、熱分解装置と測定
器を結ぶ系中に本発明のカラム装置を設置すれば、今ま
で熱分解発生ガスを極微量で測定したり、コールドトラ
ップしていたのに比して検出限界も上がり、発生ガス補
集効率もコールドトラツプより上がる。
■ When measuring pyrolysis gases, if the column device of the present invention is installed in the system connecting the pyrolysis equipment and the measuring device, it will be possible to measure extremely small amounts of pyrolysis gases or use cold traps instead of the conventional methods. The detection limit is also higher than that of a cold trap, and the efficiency of collecting generated gas is also higher than that of a cold trap.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図a,bは本発明の一実施例を示す略図で、aは捕
集濃縮時、bは脱着時を示す。 第2図及び第3図は説明用グラフである。図に於て、1
は気体濃縮用カラム、2は吸着剤、3はカラム加熱用ヒ
ータ、4,5は3方弁である。 尚、図中同一符号は同一部分を示す。第1図第1図 第2図 第3図
FIGS. 1a and 1b are schematic diagrams showing one embodiment of the present invention, in which a shows a state during collection and concentration, and b shows a state during desorption. FIGS. 2 and 3 are explanatory graphs. In the figure, 1
2 is a column for gas concentration, 2 is an adsorbent, 3 is a heater for heating the column, and 4 and 5 are three-way valves. Note that the same reference numerals in the figures indicate the same parts. Figure 1 Figure 1 Figure 2 Figure 3

Claims (1)

【特許請求の範囲】[Claims] 1 被濃縮気体の流れ方向に延在して設けられた気体濃
縮用カラムと、上記気体濃縮用カラム内部に充填された
モレキユラーシーブと、上記気体濃縮用カラムの入口お
よび出口にそれぞれ設けられ吸着時には稀薄な被濃縮気
体を上記気体濃縮用カラム内に導入し上記モレキユラー
シーブに吸着させた後上記気体濃縮用カラム外に排出す
ると共に、脱着時には上記気体濃縮用カラム内にキヤリ
ーガスを上記稀薄な被濃縮気体とは逆方向に導入し上記
モレキユラーシーブから上記気体を脱着させた後上記気
体濃縮カラム外に排出する一対の三方弁と、上記脱着時
に上記気体濃縮用カラムを加熱した上記脱着を促進する
加熱手段とを備えたことを特徴とする気体濃縮用カラム
装置。
1 A gas concentrating column provided extending in the flow direction of the gas to be concentrated, a molecular sieve packed inside the gas concentrating column, and a molecular sieve provided at the inlet and outlet of the gas concentrating column, respectively. At the time of adsorption, a dilute gas to be concentrated is introduced into the gas concentrating column, adsorbed by the molecular sieve, and then discharged outside the gas concentrating column, and at the time of desorption, the carry gas is introduced into the gas concentrating column. A pair of three-way valves that introduce the dilute gas to be concentrated in the opposite direction to desorb the gas from the molecular sieve and then discharge it to the outside of the gas concentrating column, and a pair of three-way valves that heat the gas concentrating column during the desorption. A column device for concentrating a gas, comprising a heating means for promoting the desorption.
JP51152452A 1976-12-17 1976-12-17 Column equipment for gas concentration Expired JPS6034689B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51152452A JPS6034689B2 (en) 1976-12-17 1976-12-17 Column equipment for gas concentration

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51152452A JPS6034689B2 (en) 1976-12-17 1976-12-17 Column equipment for gas concentration

Publications (2)

Publication Number Publication Date
JPS5376092A JPS5376092A (en) 1978-07-06
JPS6034689B2 true JPS6034689B2 (en) 1985-08-10

Family

ID=15540818

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51152452A Expired JPS6034689B2 (en) 1976-12-17 1976-12-17 Column equipment for gas concentration

Country Status (1)

Country Link
JP (1) JPS6034689B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03121499U (en) * 1990-03-22 1991-12-12

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03121499U (en) * 1990-03-22 1991-12-12

Also Published As

Publication number Publication date
JPS5376092A (en) 1978-07-06

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