CN101726533A - Rapid and sensitive method for detecting melamine - Google Patents

Rapid and sensitive method for detecting melamine Download PDF

Info

Publication number
CN101726533A
CN101726533A CN200810228131A CN200810228131A CN101726533A CN 101726533 A CN101726533 A CN 101726533A CN 200810228131 A CN200810228131 A CN 200810228131A CN 200810228131 A CN200810228131 A CN 200810228131A CN 101726533 A CN101726533 A CN 101726533A
Authority
CN
China
Prior art keywords
melamine
sample
sample introduction
injection port
thin slice
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.)
Granted
Application number
CN200810228131A
Other languages
Chinese (zh)
Other versions
CN101726533B (en
Inventor
李海洋
仓怀文
董璨
徐秀明
杜永斋
王贞鑫
鞠帮玉
王海龙
丛润滋
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.)
Dalian Institute of Chemical Physics of CAS
Original Assignee
Dalian Institute of Chemical Physics of CAS
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 Dalian Institute of Chemical Physics of CAS filed Critical Dalian Institute of Chemical Physics of CAS
Priority to CN 200810228131 priority Critical patent/CN101726533B/en
Publication of CN101726533A publication Critical patent/CN101726533A/en
Application granted granted Critical
Publication of CN101726533B publication Critical patent/CN101726533B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
  • Sampling And Sample Adjustment (AREA)

Abstract

The invention discloses a new method for detecting melamine. Based on an ion mobility spectrometry technology, by using the ion mobility spectrometry as a detection means and combining a simple solvent extraction pretreatment method, the method has high detection speed and sensitivity and needs only 0.5 minute for analysis and less than 5 minutes for pretreatment; and the detection limit can reach 50ppb.

Description

A kind of method of quick, sensitive detection melamine
Technical field
The present invention relates to the melamine detection method, specifically a kind of method of quick, sensitive detection melamine newly, this method is based on the ion mobility spectrometry technology, utilize ionic migration spectrometer as analysis means, utilize simple solvent extraction pretreatment technology, detection speed is fast, only want 0.5 minute analysis time, time for sample pretreatment is less than 5 minutes, and is highly sensitive, and detectability can reach 50ppb.
Background technology
Melamine (English name Melamine) is called for short triamine, is a kind of triazines nitrogen heterocyclic ring organic compound, important azacyclo-Organic Chemicals.Proterties is pure white monoclinic prism body, and is tasteless, density 1.573g/cm 3(16 ℃).354 ℃ of normal pressure fusing points (decomposition); The Fast Heating distillation, 300 ℃ of sublimation temperatures.Be dissolved in hot water, water-soluble 3G/L (20﹠amp; Ordm; C), be slightly soluble in cold water, the atomic hot ethanol that is dissolved in is insoluble to ether, benzene and phenixin, dissolves in methyl alcohol, formaldehyde, acetate, hot ethylene glycol, glycerine, pyridine etc.Low toxicity.More stable in the ordinary course of things, emit prussiate but at high temperature may decompose.
Melamine is a kind of broad-spectrum basic organic chemical industry's intermediate product, and topmost purposes is as the raw material of producing melamine formaldehyde resin (MF).Melamine can also be made fire retardant, water reducer, formaldehyde detersive etc.This resin hardness ratio Lauxite height, nonflammable, water-fast, heat-resisting, ageing-resistant, anti-electric arc, resistance to chemical attack, good insulation performance performance, glossiness and physical strength are arranged, extensively apply to industries such as timber, plastics, coating, papermaking, weaving, leather, electric, medicine.
Melamine is a kind of industrial chemicals of low toxicity.Zoopery is the result show, metabolism is very fast and can not retain in animal body for it, mainly influences urinary system.In recent years, because the defective of food and feed industry protein content method of testing, melamine often is used as food additives by illegal businessman, and with the protein content index in the lifting food inspection, so melamine also is " extract of protein " by person.2007, the contaminated incident of U.S.'s outburst pet food.Post-survey shows: mixed≤gluten powder of 6.6% melamine is that pet food causes the reason of poisoning.In September, 2008, the contaminated incident of China's outburst Sanlu baby milk powder, the infant who has caused eating contaminated milk powder produces the kidney stone illness, and its reason also is to contain melamine in the milk powder.State General Administration for Quality Supervision has promptly carried out the special examination of baby milk powder content of melamine recently in the whole nation.Special examination is this time investigated all the other 109 tame enterprises, has checked 491 batch products of these enterprises altogether.Interim check result shows, has 69 batch products of 22 tame baby milk powder manufacturing enterprises to detect the different melamine of content.Therefore quick, the sensitive detection of melamine is extremely urgent.
The method of existing detection melamine mainly comprises liquid chromatography-mass spectrography, Solid-Phase Extraction and high performance liquid chromatography coupling method, high performance liquid chromatography-diode array etc.These methods need loaded down with trivial details sample pre-treatments program, waste time and energy, and can not realize express-analysis, and detection sensitivity not high enough (2ppm magnitude).In the last few years, ion mobility spectrometry was because advantage such as its high sensitivity, express-analysis, portability and be used to the on-line analysis of industry and environment more and more.Therefore, the present invention just is used for melamine detection with ion mobility spectrometry, and detection speed is fast, and is highly sensitive.
Summary of the invention
The purpose of this invention is to provide a kind of method of new detection melamine, this method detection speed is fast, and only want 0.5 minute analysis time, and time for sample pretreatment is less than 5 minutes, and is highly sensitive, and detectability can reach 50ppb.
In order to realize quick, the sensitive detection of melamine, the present invention utilizes ionic migration spectrometer as analysis means based on the ion migrating technology, utilizes the solvent extraction method pretreatment technology, and detection speed is fast, and is highly sensitive.
A kind of method that detects melamine fast, delicately,
1) solvent extraction: testing sample is dissolved in the organic solvent, leave standstill get supernatant as sample solution for detecting, or with the filtering with microporous membrane in the following aperture of 0.1~5 μ m, confession detects filtrate as sample solution;
2) sample solution of extraction 20-50mL drops on the sample introduction thin slice, utilizes ionic migration spectrometer to detect, and measures time and peak intensity that ion arrives the ionic migration spectrometer detector;
3) melamine is dissolved in the organic solvent, melamine solution with the 0.1-10ppm standard is the standard sample solution, extract the standard sample solution of 20-50mL, drop on the sample introduction thin slice, with step 2) under the identical condition, utilize ionic migration spectrometer to detect, measure the reagent ion peak position that ion arrives the ionic migration spectrometer detector;
4) confirm step 2 by reagent ion peak position that step 3) obtained) peak intensity of the melamine among the result that obtains, further just can confirm the content of melamine.
The usage ratio of described testing sample and organic solvent is 1: 100~4: 5; Described organic solvent is for dissolving organism methyl alcohol, formaldehyde, acetate, hot ethylene glycol, glycerine and/or the pyridine of melamine; Described sample introduction thin slice is metal grid mesh, poly-tetrafluoro sheet or sample introduction paper.
Described ionic migration spectrometer is traditional uniform field migration spectrum; Mainly comprise sampling device, ionization source, reaction zone, ion gate, migration area, signal reception and detection system and gas circuit drying system, described sampling device is made of injection port and the carrier gas transfer pipeline that is arranged at the injection port outside, around the outside of injection port, be provided with hot parser, the hot parser inboard is provided with heating rod or heating tape, is inserted in the injection port during described sample introduction thin slice sample introduction.
The inboard of described hot parser is provided with temperature controller, and it is connected with heating rod or heating tape circuit; Described carrier gas transfer pipeline is made by four fluorine tube or metal tube, and the carrier gas transfer pipeline is provided with flowmeter.
Advantage of the present invention is as follows:
Compare with traditional gas chromatography, liquid phase chromatogram-mass spectrometry combination method, the means of ion mobility spectrometry as analyzing melamine are had the following advantages: the whole instrument total amount is easy to carry less than 15kg, the instrument independent operating, do not need computer and external source of the gas and liquid, be fit to on-the-spot the use, the instrument volume is small and exquisite portable; Measuring amount speed is fast, is generally less than 0.5 minute analysis time; Sample pre-treatments is required very low, equipment and the time that pre-treatment needs few (pre-service averaging time less than 8 minutes), be fit to very much the on-site quick screening that dairy produce is produced each flow process; The operating cost of instrument is very low, and consumables mainly are the required organic solvents of pre-treatment, measures the solvent that single sample consumes 25mL approximately, and its cost is lower than 1 yuan; The cost performance height of instrument, analysis speed are more suitable for the analysis of sample in batches than fast 10 times of HPLC-UV and GC-MS etc.
Description of drawings
The present invention is further detailed explanation below in conjunction with drawings and Examples:
Fig. 1 measures the ion mobility spectrometry structural representation of melamine.
Fig. 1 a sampling device structural representation;
Fig. 2 detects the migration spectrogram of pure product melamine with ion mobility spectrometry.
Fig. 3 detects the migration spectrogram of milk sample with ion mobility spectrometry.
Fig. 4 detects the migration spectrogram of powdered milk sample with ion mobility spectrometry.
Embodiment
In order to realize quick, the sensitive detection of melamine, the present invention uses ion mobility spectrometry as analysis means and the coupling of this simple sample pre-treatments technology of solvent extraction.
Ionic migration spectrometer adopts traditional uniform field migration spectrum, and its structural representation is seen Fig. 1.This instrument mainly comprises following components: sampling device 1, ionization source 2, reaction zone 3, ion gate 4, migration tube 5, make-up gas? 6 and signal receive and detection system 7.Wherein, 8 is Faraday cylinder, and 9 is amplifier, and 10 is A/D converter, and 11 is pressurized air, and 12 is data handling system (as oscillograph).
As shown in Figure 2, described sampling device is made of injection port 16 and the carrier gas transfer pipeline 15 that is arranged at the injection port outside, around the outside of injection port, be provided with hot parser 13, hot parser 13 inboards are provided with sample introduction thin slice 14 and heating rod or heating tape 17, place injection port 16 places during described sample introduction thin slice 14 sample introductions, the carrier gas of carrier gas transfer pipeline 15 outlets purges on sample introduction thin slice 14.
The inboard of described hot parser 13 is provided with temperature controller 18, and it is connected with heating rod or heating tape circuit; Described sample introduction thin slice is metal grid mesh, poly-tetrafluoro sheet and/or sample introduction paper; Described carrier gas transfer pipeline is made by four fluorine tube or metal tube 19, and the carrier gas transfer pipeline is provided with flowmeter 20;
Utilize the process of this instrument detecting melamine as follows: to extract the organic solvent extraction milk of 20-50mL and the supernatant after the milk powder, drop on the sample introduction paper, insert the injection port 16 of instrument then.The sample that contains melamine is vaporized fast by a built-in hot parser 13, and the temperature of hot parser is by temperature controller 18 controls, about 200 ℃; Pyrolysis is analysed the sample gas that obtains and is entered the general ionized region 2 of ion migration by the carrier gas carrier band of being carried by carrier gas transfer pipeline 15, and the flow of carrier gas is by flowmeter 18 controls, about 300sccm; Sample is ionized to negative ions at ionized region, and the ion gate 4 by the cycle opens enters the drift region 5 that is made of uniform electric field, obtains in the drift region separating and detects.The mobility constant of different compounds is variant, the speed difference that moves in the drift region, and they arrive the asynchronism(-nization) of detecting device.Measure time and peak intensity that ion arrives detector, just can confirm classes of compounds, and measure its content.
This method requires low to sample pre-treatments, need only with organic solvent extraction, and concrete steps are as follows: take by weighing the volumetric flask that milk powder or fresh milk 0.5g place 25mL, and with analytically pure organic solvent constant volume, ultrasonic 2 minutes, with the organic membrane filtration of 0.45m.Wherein organic solvent comprises methyl alcohol, formaldehyde, acetate, hot ethylene glycol, glycerine and pyridine etc. for dissolving the compound of melamine.
Fig. 2-4 has provided some experiment spectrograms the present invention has been given and explanation.The experiment condition of these spectrograms is: migration tube length is 6.6cm, migration electric field intensity is 500V/cm, the ion gate time of opening the door is 0.2ms, cycle is 40ms, float gas and sample carrier gas and be pressurized air, float gas velocity 400sccm, flow rate of carrier gas 300sccm through silica gel and charcoal treatment, the migration tube temperature remains on about 130 ℃ during experiment, and the injector temperature remains on about 200 ℃.
Embodiment 1
Fig. 2 has provided the migration spectrogram that detects pure product melamine with ion mobility spectrometry, and as can be seen from the figure, melamine is well detected, and the reagent ion peak is at 4.34ms, and the characteristic peak of melamine is at 8.48ms.
Embodiment 2
What Fig. 3 provided is the migration spectrogram that detects milk sample with ion mobility spectrometry.From two figure (Fig. 2 and 3) more as can be seen, this method can detect the melamine in the milk sample delicately.
Embodiment 3
What Fig. 4 provided is the migration spectrogram that detects powdered milk sample with ion mobility spectrometry.From two figure (Fig. 2 and 4) more as can be seen, this method also can detect the melamine in the milk sample delicately.

Claims (6)

1. method that detects melamine fast, delicately is characterized in that:
1) solvent extraction: testing sample is dissolved in the organic solvent, leave standstill get supernatant as sample solution for detecting, or with the filtering with microporous membrane in the following aperture of 0.1~5 μ m, confession detects filtrate as sample solution;
2) sample solution of extraction 20-50mL drops on the sample introduction thin slice, utilizes ionic migration spectrometer to detect, and measures time and peak intensity that ion arrives the ionic migration spectrometer detector;
3) melamine is dissolved in the organic solvent, melamine solution with the 0.1-10ppm standard is the standard sample solution, extract the standard sample solution of 20-50mL, drop on the sample introduction thin slice, with step 2) under the identical condition, utilize ionic migration spectrometer to detect, measure the reagent ion peak position that ion arrives the ionic migration spectrometer detector;
4) confirm step 2 by reagent ion peak position that step 3) obtained) peak intensity of the melamine among the result that obtains, further just can confirm the content of melamine.
2. method according to claim 1 is characterized in that: the usage ratio of described testing sample and organic solvent is 1: 100~4: 5.
3. method according to claim 1 and 2 is characterized in that: described organic solvent is for dissolving organism methyl alcohol, formaldehyde, acetate, hot ethylene glycol, glycerine and/or the pyridine of melamine.
4. method according to claim 1 is characterized in that: described sample introduction thin slice is metal grid mesh, poly-tetrafluoro sheet or sample introduction paper.
5. method according to claim 1, described ionic migration spectrometer are traditional uniform field migration spectrum; Mainly comprise sampling device, ionization source, reaction zone, ion gate, migration area, signal reception and detection system and gas circuit drying system, it is characterized in that: described sampling device is made of injection port and the carrier gas transfer pipeline that is arranged at the injection port outside, around the outside of injection port, be provided with hot parser, the hot parser inboard is provided with heating rod or heating tape, places injection port during described sample introduction thin slice sample introduction.
6. method according to claim 5 is characterized in that: the inboard of described hot parser is provided with temperature controller, and it is connected with heating rod or heating tape circuit; Described carrier gas transfer pipeline is made by four fluorine tube or metal tube, and the carrier gas transfer pipeline is provided with flowmeter.
CN 200810228131 2008-10-17 2008-10-17 Rapid and sensitive method for detecting melamine Expired - Fee Related CN101726533B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200810228131 CN101726533B (en) 2008-10-17 2008-10-17 Rapid and sensitive method for detecting melamine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200810228131 CN101726533B (en) 2008-10-17 2008-10-17 Rapid and sensitive method for detecting melamine

Publications (2)

Publication Number Publication Date
CN101726533A true CN101726533A (en) 2010-06-09
CN101726533B CN101726533B (en) 2012-12-05

Family

ID=42447732

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200810228131 Expired - Fee Related CN101726533B (en) 2008-10-17 2008-10-17 Rapid and sensitive method for detecting melamine

Country Status (1)

Country Link
CN (1) CN101726533B (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102323329A (en) * 2011-07-15 2012-01-18 武汉矽感科技有限公司 Method for acquiring sample molecules in object to be detected and sample introduction mechanism of ion migration spectrometer
CN103134848A (en) * 2011-12-01 2013-06-05 中国科学院大连化学物理研究所 Qualitative and semi-quantitative analysis method for sample detection by ion mobility spectrometry
CN103499633A (en) * 2013-10-15 2014-01-08 无锡艾科瑞思产品设计与研究有限公司 Method for fast detecting melamine in milk powder based on saturated milk solution
CN103512949A (en) * 2012-06-29 2014-01-15 中国科学院大连化学物理研究所 Method for detecting bisphenol A in plastic product
CN103675080A (en) * 2012-09-13 2014-03-26 中国科学院大连化学物理研究所 Headspace sampler and ion mobility spectrometry combined system
CN104111284A (en) * 2013-04-18 2014-10-22 中国科学院大连化学物理研究所 Method for rapidly sensitively detecting sodium valproate in blood
CN105510113A (en) * 2014-09-25 2016-04-20 中国科学院大连化学物理研究所 Method for improving thermal desorption efficiency of to-be-detected sample
CN105738459A (en) * 2014-12-08 2016-07-06 中国科学院大连化学物理研究所 Method for improving blood sodium valproate detection sensitivity
CN106198702A (en) * 2015-05-06 2016-12-07 中国科学院大连化学物理研究所 A kind of method of drugs in quick detection saliva

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4941958A (en) * 1989-03-08 1990-07-17 Westinghouse Electric Corp. Device and method for detecting ionic components in solution
US6239428B1 (en) * 1999-03-03 2001-05-29 Massachusetts Institute Of Technology Ion mobility spectrometers and methods
CN2927049Y (en) * 2006-02-21 2007-07-25 公安部第三研究所 Gasified substance ion transferring rate qualitative analyzer
DE102006019463A1 (en) * 2006-04-27 2007-11-08 Optimare Gmbh Ionization method in gas phase using pulse laser, useful for detecting of e.g. polar analytes and alkyl ketones, comprises ionizing a dopant with an aromatic system, forming a cationic species and detecting the cationic species

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102323329A (en) * 2011-07-15 2012-01-18 武汉矽感科技有限公司 Method for acquiring sample molecules in object to be detected and sample introduction mechanism of ion migration spectrometer
CN103134848A (en) * 2011-12-01 2013-06-05 中国科学院大连化学物理研究所 Qualitative and semi-quantitative analysis method for sample detection by ion mobility spectrometry
CN103512949A (en) * 2012-06-29 2014-01-15 中国科学院大连化学物理研究所 Method for detecting bisphenol A in plastic product
CN103675080A (en) * 2012-09-13 2014-03-26 中国科学院大连化学物理研究所 Headspace sampler and ion mobility spectrometry combined system
CN104111284A (en) * 2013-04-18 2014-10-22 中国科学院大连化学物理研究所 Method for rapidly sensitively detecting sodium valproate in blood
CN103499633A (en) * 2013-10-15 2014-01-08 无锡艾科瑞思产品设计与研究有限公司 Method for fast detecting melamine in milk powder based on saturated milk solution
CN103499633B (en) * 2013-10-15 2015-10-21 无锡艾科瑞思产品设计与研究有限公司 Based on the method for quick of melamine in the milk powder of saturated milk solution
CN105510113A (en) * 2014-09-25 2016-04-20 中国科学院大连化学物理研究所 Method for improving thermal desorption efficiency of to-be-detected sample
CN105738459A (en) * 2014-12-08 2016-07-06 中国科学院大连化学物理研究所 Method for improving blood sodium valproate detection sensitivity
CN105738459B (en) * 2014-12-08 2019-09-06 中国科学院大连化学物理研究所 A kind of method of sodium vedproate detection sensitivity in raising blood
CN106198702A (en) * 2015-05-06 2016-12-07 中国科学院大连化学物理研究所 A kind of method of drugs in quick detection saliva
CN106198702B (en) * 2015-05-06 2019-01-25 中国科学院大连化学物理研究所 A kind of method of drugs in quick detection saliva

Also Published As

Publication number Publication date
CN101726533B (en) 2012-12-05

Similar Documents

Publication Publication Date Title
CN101726533B (en) Rapid and sensitive method for detecting melamine
EP3029715B1 (en) Method used for rapid testing of highly volatile substances of very high concern in textiles
CN104713945A (en) Method for detecting explosive peroxide TATP
CN101852767A (en) Method for quickly detecting trace melamine
CN104792759A (en) Fluorescent test paper capable of rapidly detecting formaldehyde and application of fluorescent test paper
CN110174470A (en) The high-flux detection method of marine biotoxins in a kind of aquatic products
CN104007192A (en) Determination method for metal deactivator, furfural and anti-oxidant in insulating oil
CN104849373A (en) Method for testing residual amount of perfluoro caprylic acid in leather based on precolumn derivatization-high performance liquid chromatography-fluorescence detector
CN103743844A (en) Determination method of alcohol content in methanol
CN103175920A (en) Gas chromatography-mass spectrometry combined detection method for eight monohydroxy polycyclic aromatic hydrocarbons in urine
CN108845063B (en) Detection reagent combination and detection method of aquatic product additive
CN105910881B (en) A kind of micromation heat auxiliary sample pretreatment device and application detected for Surface enhanced Raman spectroscopy
CN102445507A (en) Method for determining vinyl content in methyl vinylsiloxane rubber or silicone oil
CN103134847A (en) Novel method for detecting citric acid fentanyl anaesthetic
CN105334282B (en) Co-detecting method for environmental estrogens in surface water body
CN106872629B (en) A kind of method of three nitrogen amidine contents in measurement dairy products
CN110220990A (en) A kind of method of polar organic compound in measurement airborne fine particulate matter
CN105738514A (en) Method for detecting pesticide residues through stirring rod adsorption and extraction
CN205280680U (en) Survey system of trace alkyl mercury
Guo et al. Precise evaluation of batch adsorption kinetics of plant total polyphenols based on a flow-injection online spectrophotometric method
CN107340324A (en) Using the method for the glass-carbon electrode detection L tyrosine of aminated post [5] aromatic hydrocarbons reduced graphene composite modification
CN104597180B (en) A kind of analysis method of Aromatics Extractive Project tapped oil and middle furfural content measure of raffinating oil
CN106645474A (en) Method for measuring contents of irisflorentin and piperine in Danlv kidney tonifying capsules
Rui-feng et al. Rapid determination of polyphenols in cut tobacco by microwave-assisted extraction-ultrahigh performance liquid chromatography
CN104280470B (en) The method of intermediate in liquid chromatogram measuring LLM-105 production waste water

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20121205

Termination date: 20181017

CF01 Termination of patent right due to non-payment of annual fee