JPH05302915A - Measuring apparatus for molecular weight distribution - Google Patents

Measuring apparatus for molecular weight distribution

Info

Publication number
JPH05302915A
JPH05302915A JP13203392A JP13203392A JPH05302915A JP H05302915 A JPH05302915 A JP H05302915A JP 13203392 A JP13203392 A JP 13203392A JP 13203392 A JP13203392 A JP 13203392A JP H05302915 A JPH05302915 A JP H05302915A
Authority
JP
Japan
Prior art keywords
solvent
sample
molecular weight
injector
explosion
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
JP13203392A
Other languages
Japanese (ja)
Inventor
Yukiaki Katayama
幸昭 片山
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.)
Shimadzu Corp
Original Assignee
Shimadzu 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 Shimadzu Corp filed Critical Shimadzu Corp
Priority to JP13203392A priority Critical patent/JPH05302915A/en
Publication of JPH05302915A publication Critical patent/JPH05302915A/en
Pending legal-status Critical Current

Links

Landscapes

  • Sampling And Sample Adjustment (AREA)

Abstract

PURPOSE:To measure molecular weight distribution on line. CONSTITUTION:A solvent feeding device 20 receives the drained liquid from a diluting valve 10 of a sample introducing part, whose temperature is maintained, and the drained liquid from an injector 22 of HPLC, regenerates solvent and feeds the solvent as diluting liquid to the diluting valve 10 and as a moving phase to the injector 22. The solvent feeding device 20 is an explosion-proof type and is the continuous feeder. An explosion-proof type deaerator 42 is provided between a pump 18, which feeds the solvents of the solvent feeding device 20 and a solvent tank 40 into the diluting valve 10, and a pump 28, which feeds the solvent into the injector 22.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はサイズ排除クロマトグラ
フィ(ゲル浸透クロマトグラフィGPCともいう)を用
いて分子量又は重合度の分布を測定する測定装置に関
し、特に化学工業のプロセスラインなどに接続され、プ
ロセス側からオンラインで試料を採取して分析すること
のできるプロセス用分子量分布測定装置に関するもので
ある。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a measuring device for measuring the distribution of molecular weight or degree of polymerization by using size exclusion chromatography (also called gel permeation chromatography GPC), and in particular, it is connected to a process line of the chemical industry and has a process side. The present invention relates to a molecular weight distribution measuring apparatus for a process capable of collecting and analyzing a sample on-line from.

【0002】[0002]

【従来の技術】高分子化合物試料の分子量を測定するた
めに、サイズ排除クロマトグラフィが用いられる。サイ
ズ排除クロマトグラフィでは多孔性充填剤を充填したカ
ラムに固定相と相互作用しない条件で溶剤が注入され、
試料が分子量によって分離される。研究室あるいは実験
室においては試料を溶剤で希釈してサイズ排除クロマト
グラフィ装置に注入し測定を行なっている。
Size exclusion chromatography is used to measure the molecular weight of high molecular compound samples. In size exclusion chromatography, a solvent is injected into a column packed with a porous packing material under conditions that do not interact with the stationary phase.
The samples are separated by molecular weight. In a laboratory or a laboratory, a sample is diluted with a solvent and injected into a size exclusion chromatography device for measurement.

【0003】[0003]

【発明が解決しようとする課題】しかし、プロセスライ
ンで分子量分布を測定しようとした場合、研究室用のサ
イズ排除クロマトグラフィ装置をそのままプロセス現場
に設置してプロセス側からオンラインで試料を採取して
測定することはできない。そこで、本発明はサイズ排除
クロマトグラフィ装置を用いてオンラインで分子量分布
を測定できるようにすることを目的とするものである。
However, when trying to measure the molecular weight distribution on the process line, a size exclusion chromatography device for laboratories is directly installed at the process site, and samples are taken online from the process side for measurement. You cannot do it. Therefore, an object of the present invention is to make it possible to measure the molecular weight distribution online by using a size exclusion chromatography device.

【0004】[0004]

【課題を解決するための手段】本発明はプロセス用分子
量分布測定装置とするために、分析部としてのサイズ排
除クロマトグラフィ装置と、プロセス側から試料を採取
して希釈し分析部へ導入する保温された試料導入部と、
試料導入部との間及び分析部との間で溶剤の循環流路を
形成することができ、試料導入部への希釈液及び分析部
への移動相として溶剤を供給する防爆形の溶剤連続供給
装置と、溶剤連続供給装置と試料導入部及び分析部との
間に設けられた防爆形の脱気装置とを備えている。
The present invention provides a molecular weight distribution measuring device for a process, a size exclusion chromatography device as an analysis part, and a sample which is sampled from the process side and diluted and introduced into the analysis part. A sample introduction part,
A circulation channel for the solvent can be formed between the sample introduction part and the analysis part, and the solvent is supplied as a diluent to the sample introduction part and the mobile phase to the analysis part. An apparatus and an explosion-proof deaeration device provided between the continuous solvent supply device and the sample introduction part and the analysis part.

【0005】[0005]

【作用】プロセス側から試料を採取して希釈するまでに
冷却されると試料が固化することがあるので、試料導入
部は試料が固化しない温度に保温されている。希釈液及
び移動相として使用される溶剤の供給装置は、プロセス
現場に安全に設置できるように防爆形とし、溶剤コスト
を下げるために溶剤を循環して連続供給できるようにし
ている。希釈液や移動相に気泡を含む場合はポンプヘッ
ドなどに気泡が残留して安定した流量が得られなくなる
ので、脱気装置が設けられるが、その脱気装置も安全の
ために防爆形になっている。
When the sample is cooled from the process side until it is diluted, the sample may solidify. Therefore, the sample introduction part is kept at a temperature at which the sample does not solidify. The diluting liquid and the solvent supply device used as the mobile phase are explosion-proof so that they can be safely installed at the process site, and the solvent can be circulated continuously to reduce the cost of the solvent. If the diluent or mobile phase contains air bubbles, the air bubbles will remain in the pump head, etc. and a stable flow rate will not be obtained.Therefore, a deaerator is provided, but the deaerator is also explosion-proof for safety. ing.

【0006】[0006]

【実施例】図1は一実施例を表わす。プロセスラインの
重合反応器2にはポンプ4とクロスフロー式セラミック
フィルタ6を含む循環流路が接続されている。フィルタ
6の濾過液流出口には試料ポンプ8を介して六方弁の希
釈弁10が接続されている。希釈弁10は計量ループ1
2を備え、また希釈弁10には試料を希釈するミキサ1
4が接続され、希釈液を供給する希釈液ポンプ18が接
続され、溶剤供給装置20への排出流路も接続されてい
る。濾過装置と希釈装置を含んだ部分が試料導入部であ
り、試料導入部では試料が希釈される前に固化するのを
防ぐために、試料に応じた適当な温度に保温されてい
る。その保温温度は例えば150℃〜200℃である。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT FIG. 1 shows an embodiment. A circulation flow path including a pump 4 and a cross flow type ceramic filter 6 is connected to the polymerization reactor 2 in the process line. A diluting valve 10, which is a six-way valve, is connected to the filtrate outlet of the filter 6 via a sample pump 8. The dilution valve 10 is the measuring loop 1
2, and a dilution valve 10 having a mixer 1 for diluting a sample.
4 is connected, a diluent pump 18 for supplying a diluent is connected, and a discharge flow path to the solvent supply device 20 is also connected. A portion including the filtering device and the diluting device is a sample introducing portion, and the sample introducing portion is kept at an appropriate temperature according to the sample in order to prevent the sample from solidifying before being diluted. The heat retention temperature is, for example, 150 ° C to 200 ° C.

【0007】ミキサ14の出口はサイズ排除クロマトグ
ラフィの高速液体クロマトグラフ(HPLC)のインジ
ェクタ22に接続されている。インジェクタ22は六方
切換え弁式であり、計量ループ24を備えている。ミキ
サ14からインジェクタ22に供給された試料で、カラ
ム26に注入されない試料は溶剤供給装置20へ排出さ
れる。インジェクタ22にはさらにHPLCに移動相を
供給する移動相ポンプ28と、カラム26が接続されて
いる。30は検出器、32はデータ処理装置である。
The outlet of the mixer 14 is connected to a size exclusion chromatography high performance liquid chromatograph (HPLC) injector 22. The injector 22 is of a six-way switching valve type and has a metering loop 24. The sample supplied from the mixer 14 to the injector 22 and not injected into the column 26 is discharged to the solvent supply device 20. The injector 22 is further connected to a mobile phase pump 28 that supplies a mobile phase to the HPLC, and a column 26. Reference numeral 30 is a detector, and 32 is a data processing device.

【0008】希釈弁10からの排出液とインジェクタ2
2からの排出液を受け取り、溶剤を再生して希釈弁10
への希釈液として、及びインジェクタ22への移動相と
して供給する溶剤供給装置20は防爆形で連続供給装置
となっている。溶剤供給装置20には希釈弁10及びイ
ンジェクタ22からの排出液から溶剤を気化させるため
に加熱手段36を備えたエバポレータ34、エバポレー
タ34からの溶剤蒸気を冷却して液化し溶剤に再生する
コンデンサ38、及びコンデンサ38で冷却されて再生
した溶剤を溜める溶剤タンク40が設けられている。溶
剤タンク40の溶剤を希釈弁10へ供給するポンプ18
及びインジェクタ22へ供給するポンプ28と溶剤タン
ク40の間には脱気装置42が設けられており、脱気装
置42も防爆形になっている。脱気装置42の一例は、
多孔質の合成樹脂膜からなるチューブ内に溶剤を通し、
そのチューブの外側を減圧にして分子量の小さい酸素、
窒素及び二酸化炭素を脱気できるものである。
The liquid discharged from the dilution valve 10 and the injector 2
Dilution valve 10 that receives the effluent from 2 and regenerates the solvent
The solvent supply device 20 supplied as a diluent to the injector 22 and as a mobile phase to the injector 22 is an explosion-proof continuous supply device. The solvent supply device 20 includes an evaporator 34 having a heating means 36 for vaporizing the solvent from the liquid discharged from the dilution valve 10 and the injector 22, and a condenser 38 for cooling and liquefying the solvent vapor from the evaporator 34 to regenerate the solvent. , And a solvent tank 40 for storing the solvent that has been regenerated by being cooled by the condenser 38. A pump 18 for supplying the solvent in the solvent tank 40 to the dilution valve 10.
A deaerator 42 is provided between the pump 28 and the solvent tank 40 that supply the injector 22, and the deaerator 42 is also explosion-proof. An example of the deaerator 42 is
Pass the solvent through the tube made of porous synthetic resin film,
The outside of the tube is depressurized to reduce the molecular weight of oxygen,
It can degas nitrogen and carbon dioxide.

【0009】次に、本実施例の動作について説明する。
希釈液及び移動相として利用される溶剤としては、トリ
ヒドロフラン、ベンゼン、トルエン、クロロホルム、o
−ジクロロベンゼン、1,2,4−トリクロロベンゼ
ン、o−クレゾール、N,N−ジメチルホルルアミド、
ヘキサフルオロイソプロパノールなど、試料と充填剤に
応じて選択して使用する。
Next, the operation of this embodiment will be described.
Solvents used as diluents and mobile phases include trihydrofuran, benzene, toluene, chloroform, o
-Dichlorobenzene, 1,2,4-trichlorobenzene, o-cresol, N, N-dimethylformamide,
Hexafluoroisopropanol etc. is selected and used according to the sample and filler.

【0010】オンラインでの使用に先立ち、予め分子量
が既知の標準試料を試料導入部から導入し、その溶出時
間から構成曲線を作成しておく。プロセスラインから試
料を導入するときは、試料導入部を適温に保持して試料
の固化を防いでおき、希釈弁10を実線の流路にして計
量ループ12に試料を流し、次に希釈弁10を破線の流
路に切り換えて計量ループ12中の試料を溶剤とともに
ミキサ14へ送る。このときインジェクタ22は実線の
流路にしてミキサ14からの試料を計量ループ24から
溶剤供給装置20へ流れるようにしておく。試料が計量
ループ24を通る時間を見計らってインジェクタ22を
破線の流路に切り換え、ポンプ28からの溶剤によって
試料をカラム26へ送り出す。
Prior to online use, a standard sample having a known molecular weight is previously introduced from the sample introduction part, and a constitution curve is prepared from the elution time thereof. When the sample is introduced from the process line, the sample introduction part is kept at an appropriate temperature to prevent the sample from solidifying, the dilution valve 10 is used as a flow path of the solid line to flow the sample into the measuring loop 12, and then the dilution valve 10 is used. Is switched to the flow path indicated by the broken line, and the sample in the measuring loop 12 is sent to the mixer 14 together with the solvent. At this time, the injector 22 is set as a solid flow path so that the sample from the mixer 14 flows from the measuring loop 24 to the solvent supply device 20. When the time for the sample to pass through the metering loop 24 is observed, the injector 22 is switched to the flow path indicated by the broken line, and the solvent from the pump 28 sends the sample to the column 26.

【0011】[0011]

【発明の効果】本発明では試料導入部を保温し、溶剤供
給装置と脱気装置を防爆形にしたので、フロセス現場で
オンラインで分子量分布を測定できるようになる。ま
た、溶剤を循環して連続供給できるようにしているの
で、溶剤使用量が減ってランニングコストが低減され、
溶剤供給頻度が低減して省力化を図ることができる。
According to the present invention, since the sample introduction portion is kept warm and the solvent supply device and the degassing device are explosion proof, the molecular weight distribution can be measured online at the process site. Also, since the solvent is circulated so that it can be continuously supplied, the amount of solvent used is reduced and the running cost is reduced.
The frequency of solvent supply can be reduced and labor can be saved.

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

【図1】一実施例を示す流路図である。FIG. 1 is a flow chart showing an example.

【符号の説明】[Explanation of symbols]

2 重合反応器 6 セラミックフィルタ 10 希釈弁 14 ミキサ 20 防爆形溶剤連続供給装置 22 インジェクタ 26 充填カラム 30 検出器 34 エバポレータ 38 コンデンサ 40 溶剤タンク 42 防爆形脱気装置 2 Polymerization reactor 6 Ceramic filter 10 Dilution valve 14 Mixer 20 Explosion-proof continuous solvent feeder 22 Injector 26 Packed column 30 Detector 34 Evaporator 38 Condenser 40 Solvent tank 42 Explosion-proof degasser

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 分析部としてのサイズ排除クロマトグラ
フィ装置と、プロセス側から試料を採取して希釈し分析
部へ導入する保温された試料導入部と、試料導入部との
間及び分析部との間で溶剤の循環流路を形成することが
でき、試料導入部への希釈液及び分析部への移動相とし
て溶剤を供給する防爆形の溶剤連続供給装置と、溶剤連
続供給装置と試料導入部及び分析部との間に設けられた
防爆形の脱気装置とを備えたことを特徴とするプロセス
用分子量分布測定装置。
1. A size exclusion chromatography apparatus as an analysis unit, a heat-insulated sample introduction unit for collecting a sample from the process side, diluting it, and introducing it into the analysis unit, and between the sample introduction unit and the analysis unit. It is possible to form a circulation channel of the solvent with, the explosion-proof solvent continuous supply device for supplying the solvent as a mobile phase to the diluent and the analysis part to the sample introduction part, the solvent continuous supply device and the sample introduction part and An apparatus for molecular weight distribution measurement for a process, comprising an explosion-proof deaeration device provided between the analysis unit and the analysis unit.
JP13203392A 1992-04-24 1992-04-24 Measuring apparatus for molecular weight distribution Pending JPH05302915A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13203392A JPH05302915A (en) 1992-04-24 1992-04-24 Measuring apparatus for molecular weight distribution

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13203392A JPH05302915A (en) 1992-04-24 1992-04-24 Measuring apparatus for molecular weight distribution

Publications (1)

Publication Number Publication Date
JPH05302915A true JPH05302915A (en) 1993-11-16

Family

ID=15071931

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13203392A Pending JPH05302915A (en) 1992-04-24 1992-04-24 Measuring apparatus for molecular weight distribution

Country Status (1)

Country Link
JP (1) JPH05302915A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7217360B2 (en) 2000-12-28 2007-05-15 Cohesive Technologies Inc. Multi column chromatography system

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7217360B2 (en) 2000-12-28 2007-05-15 Cohesive Technologies Inc. Multi column chromatography system

Similar Documents

Publication Publication Date Title
Cazes Gel permeation chromatography—Part 1
US7213443B2 (en) Process and apparatus for providing gas for isotopic ratio analysis
US6447575B2 (en) Method and apparatus for gas chromatography analysis of samples
JP3725441B2 (en) Method for analyzing impurities in a gas stream
US6293995B2 (en) Chromatograph having a gas storage system
US3751880A (en) Carrier gas separating unit
FI95319C (en) Method and apparatus for sampling
JPH05302915A (en) Measuring apparatus for molecular weight distribution
Madras et al. A new technique for measuring solubilities of organics in supercritical fluids
GB2421792A (en) Process and apparatus for analysis of a gaseous substance
JP2005249691A (en) Gas chromatograph unit and exhaust gas analytical method
Matsumoto et al. Fundamental conditions in pressure-programmed supercritical fluid chromatography-mass spectrometry and some applications to vitamin analysis
Moskvin et al. Analytical application of liquid-gas and liquid-gas-solid chromatography
US3171274A (en) Sampling method for gas chromatographic analyzer
EP0572968A2 (en) Method and device for the preparation of liquid samples for analysis
Villén et al. Very large volume sample introduction in capillary gas chromatography using a programmed temperature injector for pesticide analysis
JPS63265164A (en) Chromatographic analysis method
Ikushima et al. Measurement and linear correlation of the solvent polarity parameters of supercritical carbon dioxide and its cosolvent systems
US5327779A (en) Vapor pressure measurement by gas saturation for mixture
US20220011201A1 (en) Method and an apparatus for determining isotope relationships
JPH08201363A (en) Sample concentrating device for analysis
JPS62151754A (en) Treatment of carrier for chromatography
Greenwalt et al. Transmission of organic molecules by a silicone membrane gas chromatograph/mass spectrometer interface
US4992083A (en) Apparatus for intermediate enrichment of trace substances from a gas stream in a cold trap, and chromatography arrangement provided therewith
JPH05232095A (en) Continuous automatic analyzer for volatile hydrocarbon