CN201076777Y - Subsequent type stimulant moving bed - Google Patents

Subsequent type stimulant moving bed Download PDF

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Publication number
CN201076777Y
CN201076777Y CNU2007200233454U CN200720023345U CN201076777Y CN 201076777 Y CN201076777 Y CN 201076777Y CN U2007200233454 U CNU2007200233454 U CN U2007200233454U CN 200720023345 U CN200720023345 U CN 200720023345U CN 201076777 Y CN201076777 Y CN 201076777Y
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CN
China
Prior art keywords
chromatographic column
eluent
moving bed
eluant
utility
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 - Fee Related
Application number
CNU2007200233454U
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Chinese (zh)
Inventor
王成福
王星云
田强
解学美
张念强
张小宁
杜瑞峰
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.)
Shandong Futian Pharmaceutical Co Ltd
Original Assignee
Shandong Futian Pharmaceutical Co Ltd
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 Shandong Futian Pharmaceutical Co Ltd filed Critical Shandong Futian Pharmaceutical Co Ltd
Priority to CNU2007200233454U priority Critical patent/CN201076777Y/en
Application granted granted Critical
Publication of CN201076777Y publication Critical patent/CN201076777Y/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

The utility model relates to a subsequent type simulated moving bed, which comprises a chromatographic column, a circulating pump, a material delivery system, a flow gage, a pressure gage, a pressure marinating valve, an auto-control valve and a control system. The utility model is characterized in that the chromatographic column is formed by 4-10 chromatographic columns which are mutually connected in series, the heads and the tails of the chromatographic columns are connected to form a closed system, the upper portion of each chromatographic column is provided with a feed hole and an eluent inlet hole, the lower portion of each chromatographic column is provided with three-type outlets of outgoing components, auto-control valves are arranged on a feed, a discharge and a circulate pipelines, circulating pumps are mounted in the circulate pipelines, heat of each chromatographic column and each pipeline is preserved by jacketed insulation water or other insulation material, and the system which is constant in some range is guaranteed when the system is operated. The utility model has the advantages of simple structure and simple operation, which can achieve the separation of triad component.

Description

Sequential simulated moving bed
Technical field
The utility model relates to a kind of separation equipment.
Background technology
At present, existing simulation moving-bed equipment is that many root chromatogram columns are contacted, form a kind of splitter of endless of simulation, pass through the input and output material on diverse location continuously then, reach purpose, because the pattern of its separation is fixed separating substances, so can only carry out the separation of binary composition, and for the separation of ternary component, and separate the material of major constituent in the centre, then do not have and separate the purpose of purifying.
Summary of the invention
The purpose of this utility model is at above weak point, provide a kind of simple in structure, easy to operate, can to realize that ternary component separates sequential simulated moving bed.
Of the present invention sequential simulated moving bedly form by chromatographic column, circulating pump, material-transporting system, flowmeter, Pressure gauge, pressure maintaining valve, internally piloted valve and control system.Its technical scheme is that chromatographic column is connected in series by the 4-10 root and forms, the closed-system that becomes head and the tail to connect, on every root chromatogram column, be provided with charging, advance two mouths of eluant, eluent, below every root chromatogram column, be provided with three classes and flow out the component outlet, this three class flow out component be respectively before impurity part, main component part and rear impurity part, isolated this three classes component enters respectively in separately the storage tank.On the outlet line of three classes outflow component pressure maintaining valve is installed all, band extrudes material, guarantees the stability and the qualification of discharging, and the pressure demonstration is finished by Pressure gauge.On charging, discharging, pipeloop, be provided with internally piloted valve, circulating pump is installed in pipeloop, according to the switch time and the order of PLC procedure auto-control internally piloted valve and circulating pump.Charging with advance eluant, eluent and finish, and the size control charging by pilot plunger length and flowmeter and advance the amount of eluant, eluent by plunger type metering pump.Each chromatographic column and pipeline are incubated with chuck insulation water or other insulation material, the assurance system when operation temperature constant within certain scope.
Good effect of the present utility model is separation simple in structure, easy to operate, that can realize ternary component.
Description of drawings
Below in conjunction with drawings and Examples the utility model is further specified:
Accompanying drawing 1 is the utility model structural representation;
1I chromatographic column, 2II chromatographic column, 3III chromatographic column, 4IV chromatographic column, 5V chromatographic column, 6VI chromatographic column, 7 separate raw materials jars, 8 eluant, eluent jars, 9 preceding impurity storage tanks, 10 middle major constituent storage tanks, 11 rear impurity storage tanks, 12 advance separate raw materials pump, 13 and advance eluant, eluent pump, 14 circulating pumps, 15 internally piloted valves, 16 flowmeters, 17 pipelines, 18 Pressure gauges, 19 pressure maintaining valves among the figure.
The specific embodiment
The import of separate raw materials pump (12) is connected with separate raw materials jar (7), and outlet links to each other with the import of each chromatographic column, and the import of eluant, eluent pump (13) is connected with eluant, eluent jar (8), exports to link to each other with the import of each chromatographic column.The outlet of a last root chromatogram column connects threeway and four-way, and one of them connects the import of next root chromatogram column, and one links to each other with preceding impurity storage tank (9), and one links to each other with middle main component storage tank (10), and one links to each other with rear impurity storage tank (11).The import of circulating pump (14) links to each other with the outlet of VI chromatographic column, and outlet links to each other with the import of I chromatographic column.All connecting lines (17) all select for use stainless steel tube to connect, the import of each chromatographic column, outlet all are connected with internally piloted valve (15), all internally piloted valves are connected with computer system by data wire with circulating pump (14), in computer system PLC program, configure the switch time and order of each internally piloted valve and circulating pump (14), the inlet of the outlet of separate raw materials pump (12), eluant, eluent pump (13) and preceding impurity storage tank (9), middle main component storage tank (10), rear impurity storage tank (11) all is equipped with flowmeter (16), indication flow size; The outlet of separate raw materials pump (12), eluant, eluent pump (13), the import and export of circulating pump (14) and the outlet of each chromatographic column all are equipped with Pressure gauge (18), indicated pressure size.
During work, adopt discontinuous charging and discharging, the mode of discontinuous complete alternation liquid stream is moved, and on traditional simulation moving-bed Equipment Foundations, each step of separating in the past is divided into three present sub-stepping row:
1, charging, extraction step: advance raw material and eluant, eluent, extract anterior impurity out;
2, the complete alternation step: chromatogram column system carries out complete alternation;
3, the wash-out step: advance eluant, eluent, wash out rear portion impurity.
Like this, during operation, drive separate raw materials pump (12) and eluant, eluent pump (13), advance separate raw materials from the import of III chromatographic column, advance eluant, eluent from the import of I chromatographic column, go out preceding impurity component from the outlet of I chromatographic column, enter in the preceding impurity storage tank (9), go out the rear impurity component from the outlet of V chromatographic column, enter in the rear impurity storage tank (11), the time of being advanced separate raw materials and eluant, eluent by the PLC procedure auto-control of computer is 350 seconds, time then, close separate raw materials pump (12) and eluant, eluent pump (13), by the PLC procedure auto-control open cycle pump (14) of computer and all internally piloted valves on the pipeloop, time is 650 seconds, system is in the complete alternation state, at this moment, neither also not discharging of charging, time then, close circulating pump (14), drive eluant, eluent pump (13), advance eluant, eluent from the import of II chromatographic column, go out middle main component from the outlet of I chromatographic column, enter in the middle main component storage tank (10), the time of being advanced eluant, eluent by the PLC procedure auto-control of computer is 40 seconds, time is then driven separate raw materials pump (12), advances separate raw materials from the import of IV chromatographic column, advance eluant, eluent from the import of III chromatographic column, impurity component before going out from the outlet of II chromatographic column before entering in the impurity storage tank (9), goes out the rear impurity component from the outlet of VI chromatographic column, enter in the rear impurity storage tank (11), by such reruning, preceding impurity in the separate raw materials and rear impurity be to the operation of the front and back of the main component in centre, we just can from corresponding outlet continuously extracting go out preceding impurity and rear impurity, middle main component is extracted when advancing eluant, eluent, reaches the purpose of separation of tertiary component with this.

Claims (2)

  1. One kind sequential simulated moving bed, form by chromatographic column, circulating pump, material-transporting system, flowmeter, Pressure gauge, pressure maintaining valve, internally piloted valve and control system; It is characterized in that chromatographic column is connected in series by the 4-10 root forms, the closed-system that becomes head and the tail to connect, on every root chromatogram column, be provided with charging, advance two mouths of eluant, eluent, below every root chromatogram column, be provided with three classes and flow out the component outlet, on charging, discharging, pipeloop, be provided with internally piloted valve, circulating pump is installed in pipeloop, and each chromatographic column and pipeline are incubated with chuck insulation water, the assurance system when operation temperature constant within certain scope.
  2. 2. described sequential simulated moving bed according to claim 1, it is characterized in that on the outlet line of three classes outflow component, pressure maintaining valve being installed all.
CNU2007200233454U 2007-06-14 2007-06-14 Subsequent type stimulant moving bed Expired - Fee Related CN201076777Y (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNU2007200233454U CN201076777Y (en) 2007-06-14 2007-06-14 Subsequent type stimulant moving bed

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNU2007200233454U CN201076777Y (en) 2007-06-14 2007-06-14 Subsequent type stimulant moving bed

Publications (1)

Publication Number Publication Date
CN201076777Y true CN201076777Y (en) 2008-06-25

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Family Applications (1)

Application Number Title Priority Date Filing Date
CNU2007200233454U Expired - Fee Related CN201076777Y (en) 2007-06-14 2007-06-14 Subsequent type stimulant moving bed

Country Status (1)

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CN (1) CN201076777Y (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101940850A (en) * 2010-09-29 2011-01-12 西安航天华威化工生物工程有限公司 Sequential simulated moving bed
CN103071312A (en) * 2013-02-05 2013-05-01 山东兆光色谱分离技术有限公司 Intermittent chromatographic separation device and method
CN104587706A (en) * 2014-12-11 2015-05-06 山东福田药业有限公司 Method for refining xylose hydrolysate
CN111909123A (en) * 2019-05-07 2020-11-10 中国石油化工股份有限公司 Method and device for continuously separating and purifying 5-hydroxymethylfurfural and derivatives thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101940850A (en) * 2010-09-29 2011-01-12 西安航天华威化工生物工程有限公司 Sequential simulated moving bed
CN101940850B (en) * 2010-09-29 2012-08-29 西安航天华威化工生物工程有限公司 Sequential simulated moving bed
CN103071312A (en) * 2013-02-05 2013-05-01 山东兆光色谱分离技术有限公司 Intermittent chromatographic separation device and method
CN104587706A (en) * 2014-12-11 2015-05-06 山东福田药业有限公司 Method for refining xylose hydrolysate
CN111909123A (en) * 2019-05-07 2020-11-10 中国石油化工股份有限公司 Method and device for continuously separating and purifying 5-hydroxymethylfurfural and derivatives thereof

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C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20080625

Termination date: 20110614