JPS5932861A - Liquid chromatographic mass analyzer - Google Patents

Liquid chromatographic mass analyzer

Info

Publication number
JPS5932861A
JPS5932861A JP57143630A JP14363082A JPS5932861A JP S5932861 A JPS5932861 A JP S5932861A JP 57143630 A JP57143630 A JP 57143630A JP 14363082 A JP14363082 A JP 14363082A JP S5932861 A JPS5932861 A JP S5932861A
Authority
JP
Japan
Prior art keywords
nozzle
electric field
effluent
strong electric
atomization
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
Application number
JP57143630A
Other languages
Japanese (ja)
Inventor
Tokuo Mizuno
水野 悳夫
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.)
Jeol Ltd
Original Assignee
Jeol Ltd
Nihon Denshi KK
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 Jeol Ltd, Nihon Denshi KK filed Critical Jeol Ltd
Priority to JP57143630A priority Critical patent/JPS5932861A/en
Publication of JPS5932861A publication Critical patent/JPS5932861A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/62Detectors specially adapted therefor
    • G01N30/72Mass spectrometers
    • G01N30/7233Mass spectrometers interfaced to liquid or supercritical fluid chromatograph
    • G01N30/724Nebulising, aerosol formation or ionisation
    • G01N30/726Nebulising, aerosol formation or ionisation by electrical or glow discharge

Landscapes

  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
  • Electron Tubes For Measurement (AREA)

Abstract

PURPOSE:To achieve a smooth and stable atomization even in a limited flow rate by applying a strong electric field near an emission nozzle, which has the direction the same as the jetting direction of an effluent. CONSTITUTION:An effluent fed through a feed tube 12 is injected and atomized into a low pressure glass tube 1 from an emission nozzle 2. At the same time, a spray gas is injected in the direction of the emission nozzle 4 from the perimeter of the nozzle 2 through an air blow tube 13 to promote the atomization. A circular electrode 15 is arranged near the emission nozzle 4. When a negative high voltage is applied from a power source 16 to provide a strong electric field near the nozzle 2, a solvent in the effluent appearing at the nozzle tip is polarized to be charged and so attracted by the strong electric field to jet out of the nozzle 2 with a force thereby enabling an extremely smooth atomization even in a limited flow rate.

Description

【発明の詳細な説明】 本光明は発明り]J!1〜グラフと質量分析装置を結合
した装着(こ関し、特に液体り[コマトゲラフの流出液
を霧化しく質量分析装置へ導入するようにした装置に関
する。
[Detailed description of the invention] This light is an invention] J! 1 - Relating to a device that combines a graph and a mass spectrometer, particularly a device that atomizes and introduces the effluent of a liquid column into a mass spectrometer.

多成分混合試料を分離し−C分析7;るため【こりIJ
7トグラノは有用な装置であり、特(こその検出手段ど
しC質量分析装置を結合りれば分子 −m−t′1分子
構造に関づる情報を取1qりることがC′きる。現r1
まCにガスク[lマドグラフとj’4 ii分(11装
置を稈、合した装置は広く普及しCいるか、液体り[l
マI・グラ八日l用分析装置を結合した装置は、液体を
質量分析装置へ導入し% IJればならない関係1一様
々な1−人が必要(゛、近4[種々の17式か試みら+
1Cいる段階である。
To separate a multi-component mixed sample -C analysis 7;
7 tograno is a useful device, especially if it is coupled with a mass spectrometer (a detection means), it is possible to obtain information about the molecular structure of the molecule -m-t'1. Current r1
In addition, gask [l madograph and j'4
A device that combines a mass spectrometer and a mass spectrometer requires a variety of personnel (1-1) to introduce the liquid into the mass spectrometer. Attempt+
It is at the stage of 1C.

第1図はでの・)らの−7’J式の構造を承り略図で、
図中1は内部か真空ポンプによりIJI気されるガラス
管C7t6る。該刀ラス管中には導電I11祠利(Cき
た出q・1ノズル2が挿入され、図示しイ1い液体り1
1マトグラノl)+ iらの流出液がその先端から”f
l !Ii する3、3は過冷N1並びに)り染防止の
ためぞの先端部を1111熱するためのヒータである。
Figure 1 is a schematic diagram of the -7'J formula of Deno.) et al.
In the figure, 1 is a glass tube C7t6 which is internally aerated by a vacuum pump. A conductive I11 nozzle 2 is inserted into the lath tube, and a liquid 1 as shown in the figure is inserted.
The effluent of 1 matograno l) + i et al.
l! Ii 3, 3 is a heater for heating the tip part 1111 to prevent supercooling N1 and dyeing.

出射ノズル2 /、+”:T>低圧のカラス管内へ噴出
した流出液(61、霧状になり、更に気化しくガラス管
1の※i1部にトi1シ2ノスル21ご苅向しく配置、
9?されlこ入側ノズル1へ導入さね、流路5)41′
lしC(A電源)1.1ツク0内のイΔン化室7へ后か
れ(イオン化される、1ε3は流路4を加熱づるI、二
めの1て一ター(−ある。
Output nozzle 2 /, +": T > The effluent jetted into the low-pressure glass tube (61, becomes a mist, further vaporizes, and is placed in the *i1 part of the glass tube 1 so that the nozzle 21 is facing towards the rear.
9? The flow path 5) 41' is introduced into the inlet side nozzle 1.
The first C (A power supply) 1.1 is returned to the ionization chamber 7 in the first block 0 (to be ionized), and the second one is ionized.

1111かる構成を持つ従来例(は、ノズル2にりえる
一1ンダクタンスを流出液の流量に合ゎ1iて、流量が
多い場合には人さく、又流h1が少い場合には小さくづ
る必要がある。どころが、流早に合ゎUに−]ンダクタ
ンスを小さくシ(ゆくと、目づまり等tM−,J、り霧
化が安定しく起こり難く、良好なIIT IIFflが
1!7ら罎1ないtl−果どイi: ツー(いI、:。
A conventional example with such a configuration (1111) is the case where the inductance applied to the nozzle 2 is adjusted to the flow rate of the effluent, and when the flow rate is high, it is necessary to increase the inductance, and when the flow rate h1 is small, it is necessary to decrease the inductance. However, if the inductance is reduced quickly, clogging, etc., and atomization will not occur stably, and a good IIT IIFfl will be 1!7. 1 Not tl-Kadoi: Two (I,:.

本発明は(二の貞に鑑みてなされたものであり、fli
t>Jノズル先端部に流出液の噴出方向と同じ方向を持
つ強電Wを印加づることにJ、す■]ンダクタンスを小
さり()だ場合c′ら霧化を安定に行うことの(きる液
体り(17トグラフ質耐分析装置を捉供づることを1−
1的どじでいる。以−ト本発明の一実施例を添f−1図
面(J基3さ訂述づる。
The present invention has been made in view of the second principle, and is
t>J Applying a strong electric current W having the same direction as the ejecting direction of the effluent to the tip of the nozzle will result in stable atomization from c′ if the inductance is small (). 1-1 to capture and provide a liquid container (17)
I'm on target. An embodiment of the present invention is hereinafter described in attached drawing F-1 (J-3).

第2図は木荏明の 実施例の構成を承り断面図てあ(つ
、第′1図ど同一の構成要素には同一番号がイー1され
くいる。第2図に、13い(力5ノス♀へ1(ま1.t
(本0に取イ・11ノられると共に、ぞの内部(よ]]
1−タリーポンプ1によ−)で真空tel気され(いる
。、1 ’I it基体9に聞(〕ら11に穴へ介1ノ
(カラス?31内/\1Φ人された絶縁ガイドC,その
内部(、、L(ま出IJJノズル21\流出液を運ぶ送
液管12及び送気i′11ζうが挿入されCいる。この
送液管′12(よ送気管1ζ3の中を通る二]重管椙造
どなっ一’Ca−3す、パル1”l /1及び送気管1
3を介しくヘリウム等の噴霧力スか+Aられる。前記大
川ノズル4の近傍illは、該ノズ゛ルを囲むように円
形型44i 15が配置される1、該円形型(船15に
は電源′16より口の凸型11が印加さ1;(Aタリ、
この点(、二本発明の人さく4: 1h徴が(bる。1
7は絶縁力イド11を矢印jj向に移動さけ、出用ノズ
ルと大剣ノズルの間隔を調11ハするI、:めの2ノf
(ある。
Figure 2 is a cross-sectional view of the configuration of Emei Ki's embodiment (the same components as in Figure '1' are numbered the same). 5 Nos ♀ to 1 (Ma1.t
(I was taken to book 0 and 11, and inside the house (yo)]
1-Tally pump 1) is used to vacuum the insulation guide C. Inside it (,,L), the IJJ nozzle 21\liquid feed pipe 12 carrying the effluent and the air feed pipe 1ζ are inserted. 2] Juukan Suzou Donatsu'Ca-3, Pal 1"l/1 and air pipe 1
The spray force of helium etc. is +A through 3. In the vicinity of the Okawa nozzle 4, a circular mold 44i 15 is arranged so as to surround the nozzle (1). A Tari,
This point (2) The human structure of the present invention 4: 1h characteristics (b. 1
7, move the insulating force id 11 in the direction of the arrow jj, and adjust the distance between the output nozzle and the large sword nozzle.
(be.

上述の如き構成におい−(、送′a法′12をfl 1
.、−て送られる流出液は出用ノズル27]I Lr低
月の刀−ノス管1内へIlO出し霧化されるが、同+1
.’i l−:送気管′131を介し℃噴霧ガスがノズ
ル2の周囲から八〇・1.ノズル’I (7) /’J
向へ噴出iJるI、=め、霧化が(W進されると共LJ
 iff ’Jノスル2からの流出液の噴出・霧化が入
用ノズル4のjj向へ向(〕(ijわれるよう方向11
がl)えら1する。
In the configuration as described above, the sending method '12 is fl 1
.. , - The effluent sent through the outlet nozzle 27] I Lr Low Moon Sword - IlO is discharged into the Nos tube 1 and is atomized, but the same +1
.. 'i l-: The atomized gas flows from around the nozzle 2 through the air supply pipe '131 to 80.1. Nozzle 'I (7) /'J
When the atomization is ejected in the direction of
if 'The jetting and atomization of the effluent from the J nozzle 2 is directed to the jj direction of the input nozzle 4 () (i)
(l) gills 1.

と(二ろ(・、液体り1−1ン1へグラノC使用される
溶媒は通常枠171を持つ。ぞのためノズル2の近(力
に強電Wを印11++ するど、ノズル先端から顔を出
した流出液中の溶媒(,1,その強電界により分(船し
て電荷を右りる状態とイTす、強電界に引きっ(Jられ
(ノズル21)s lら飛び出り1j向の力を受1ノる
。従ってこの力は霧化を(jj)進りるプノ向に動くこ
とになり、電界8.印加しない場合に比べ、霧化は流量
が少い場合Cb捗め(スムーズ(5行われることに’c
′にる。
(2ro(・、Liquid 1-1-1 to Grano C The solvent used usually has a frame 171. Therefore, near the nozzle 2 (mark the power with a strong electric W 11++). However, from the nozzle tip to the face The solvent in the effluent (, 1) is pulled by the strong electric field (nozzle 21) and jumps out. Therefore, this force causes the atomization to move in the direction of (jj), and compared to the case where no electric field is applied, the atomization progresses at Cb when the flow rate is small. (smoothly (5 to be done)
'Niru.

不発明石の実験Cは、ノズル間の距離5へ・7 Ill
m(、電J4i i 5に 21<\/前後の電L「を
印加した時、1 ()/lΩ5、・′分の流…cも極め
−C細かい霧が安定しく1!1らね、ぞ11以[・の流
量(” t)−1公使用Cきることが(准認U−き/に
Inventive stone experiment C, the distance between nozzles is 5 to 7 Ill
m(, when applying an electric current of around 21 < \/ to J4i i 5, a flow of 1 ()/l Ω5, ·' minutes...c is also extremely fine - C fine mist stably flows 1!1, The flow rate of 11 or more ("t)-1 can be used for public use (approval U-ki/).

この様にしく細かい霜どなり更に気化された流出液(ま
nn霧万スどJ(c=人入用スル1へ向かうが、ぞの途
中4′比較的分−r場の小さい1lrA f%ガス及び
溶媒は比較的分子量の人さい溶質に比へ〒い速度(”周
囲にlIi、散し、[1−タリーポンプ’I OL、二
よ−)C優先的に除去さねる。そのため、溶質は素綿さ
れた状態4−入用ノズル4へ人q・1シ、−イオン化室
7へ導入され(イオン化される。
In this way, there was a fine frost, and the vaporized effluent was further vaporized (mann mist). and solvents tend to preferentially remove relatively small solutes with relatively high molecular weights. Cotton cotton state 4 - q.1 people are introduced into the use nozzle 4 - Introduced into the ionization chamber 7 (ionized).

以ト5工述した如く本発明にJ、れは、+lj Q=1
ノスルの)11傍に流出液の噴出方向と同じプ)向を持
つ強電界を印加づることにより、少い流r7tでt)ス
ノ、−ズに安定した霧化を行うことの(さる液体り1.
1 :、7 トゲラフυ1量分析装置が実現される。
As described in Section 5 below, in the present invention, J is +lj Q=1
By applying a strong electric field with the same direction as the ejecting direction of the effluent to the side of the nozzle, stable atomization can be achieved in the nozzle with a small flow rate. 1.
1:,7 A spindle-shaped υ1 quantity analyzer is realized.

尚、奉ずで明は上述した実施例に限定される(■となく
幾多の変形が可能である。
It should be noted that the details are limited to the above-mentioned embodiments (numerous modifications are possible without *).

例えは、円形電極153を設(Jるかわり(ご大川ノズ
ル4の先端部を電極構造どし、ぞれ(、凸型月を印加り
るようにし−U ’b出川用スル2のNJ、 II I
ご;ii6 ?r;界を中力1し」ることができる〔
For example, set the circular electrode 153 (instead of J), change the tip of the Okawa nozzle 4 to an electrode structure, and apply a convex moon to the NJ of the Degawa nozzle 2. II I
Go;ii6? r: You can "turn the world to 1" [

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

第1図は従来装置の構成4示11gi面図、第2図(ま
本発明の一実施例の構成を小+J jtJi而図(面(
する0、1ニガシス管、2:出片1ノズル、 4:大剣ノス゛ル、7:イオン化室、 10 : +、+−タリーポンプ、11:絶縁ガイド、
12:送液管、15:円形71(極、 ′IG:電源。 特れ1出願人 11本電子株式会社 代表省 伊藤−人
Figure 1 is a side view showing the configuration of a conventional device, and Figure 2 is a side view showing the configuration of an embodiment of the present invention.
0, 1 Nigasis tube, 2: 1 nozzle, 4: Large sword nozzle, 7: Ionization chamber, 10: +, +- tally pump, 11: Insulation guide,
12: Liquid feeding pipe, 15: Circular 71 (pole, 'IG: Power supply. Special 1 Applicant 11 Hon Electronics Co., Ltd. Representative Ministry Ito-jin

Claims (1)

【特許請求の範囲】 1、真空ポンプに」、−)て排気される低圧室と、該低
圧室内へ液体り[1ン1ヘゲラフからの流出液を噴出さ
けるための出射ノズルと、該低1−1室内に該出0=1
ノスルど夕・1向し−(配置される入射ノズルと、該入
用ノズルど質f11分析装F1のイオン源を結ぶ流路ど
を(頼え、前記出f’lJノスルの近傍に流出液の噴出
yj向を持つ強電界を印加り−るようにしたことを特徴
とりる液体り[−171−グラノ質弔分析装岡。 2、金属性の出射ノズルと、入用ノズルの周囲に配置し
た対向電極との間に高電圧を印加りることにより前記強
電界を5’t 41EさUた特許請求の範囲第1項記載
の液体クロマ1〜グラフ質量分析装置。
[Claims] 1. A low-pressure chamber that is evacuated by a vacuum pump; −1 The corresponding output in the room 0 = 1
The flow path connecting the inlet nozzle to be placed and the ion source of the analyzer F1 (where the input nozzle is) Liquid liquid [-171-grano material analysis device] characterized by applying a strong electric field with ejection direction yj. 2. Arranged around the metallic output nozzle and the input nozzle. The liquid chroma 1 to graph mass spectrometer according to claim 1, wherein the strong electric field is reduced by applying a high voltage between the electrode and the counter electrode.
JP57143630A 1982-08-18 1982-08-18 Liquid chromatographic mass analyzer Pending JPS5932861A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57143630A JPS5932861A (en) 1982-08-18 1982-08-18 Liquid chromatographic mass analyzer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57143630A JPS5932861A (en) 1982-08-18 1982-08-18 Liquid chromatographic mass analyzer

Publications (1)

Publication Number Publication Date
JPS5932861A true JPS5932861A (en) 1984-02-22

Family

ID=15343218

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57143630A Pending JPS5932861A (en) 1982-08-18 1982-08-18 Liquid chromatographic mass analyzer

Country Status (1)

Country Link
JP (1) JPS5932861A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0298662A (en) * 1988-10-05 1990-04-11 Hitachi Ltd Ion extracting and analyzing apparatus

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0298662A (en) * 1988-10-05 1990-04-11 Hitachi Ltd Ion extracting and analyzing apparatus

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