CN111141848A - Content determination method of permanent violet - Google Patents

Content determination method of permanent violet Download PDF

Info

Publication number
CN111141848A
CN111141848A CN202010004216.0A CN202010004216A CN111141848A CN 111141848 A CN111141848 A CN 111141848A CN 202010004216 A CN202010004216 A CN 202010004216A CN 111141848 A CN111141848 A CN 111141848A
Authority
CN
China
Prior art keywords
permanent violet
column
content
measuring
flow rate
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
CN202010004216.0A
Other languages
Chinese (zh)
Inventor
张霄鹏
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.)
Hangzhou Ruixu Technology Group Co Ltd
Original Assignee
Hangzhou Ruixu Technology Group 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 Hangzhou Ruixu Technology Group Co Ltd filed Critical Hangzhou Ruixu Technology Group Co Ltd
Priority to CN202010004216.0A priority Critical patent/CN111141848A/en
Publication of CN111141848A publication Critical patent/CN111141848A/en
Pending legal-status Critical Current

Links

Images

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

Landscapes

  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)

Abstract

The invention relates to a method for detecting chemicals, in particular to a method for measuring the content of permanent violet. The invention adopts a liquid chromatograph method for determination, adopts a diode array detector, and has the following detection conditions: the detection wavelength is 593 nm, the chromatographic column is a reversed phase C18 column, the mobile phase is tetrahydrofuran, the flow rate is 0.8-1.2 ml/min, and the sample injection volume
Figure DDA0002354626350000011
Microliter, column temperature of
Figure DDA0002354626350000012
The method has the advantages of good reproducibility, scientificity, advancement and applicability of the determination method, more accuracy in the aspect of the content precision of the permanent violet, and better application to downstream users for checking the purity of the permanent violet.

Description

Content determination method of permanent violet
Technical Field
The invention discloses a method for detecting chemicals, and particularly relates to a method for measuring the content of permanent violet.
Background
Permanent Violet RL, the English name of which is Pigment Violet 23, the CAS number of which is 6358-30-1, the molecular formula of which is C34H22Cl2N4O2, the molecular weight of which is 589.47, is blue Violet powder with bright color, is insoluble in water, is stable in dimethyl sulfoxide, the decomposition temperature of which is more than 322 ℃, and the relative density (d20) of which is 1.5. It is non-flammable and non-corrosive. The permanent violet has high tinting strength, excellent heat resistance, sun resistance and sublimation resistance. Can be used for coloring paint, ink, rubber and plastic and for coloring synthetic fiber stock solution. How to accurately determine the content of the permanent violet is particularly important, and at the present stage, no literature exists in the method for determining the content of the permanent violet.
The problems of the prior art are that the determination is not carried out: the permanent violet RL is a high-grade organic pigment of dioxazine class. The color paste has the characteristics of outstanding coloring strength and brightness, excellent heat resistance and penetration resistance, good light fastness and excellent performance, has wide application range, is a popular variety in the fields of various coatings, plastics, organic glass, rubber, textile printing, solvent amount, water-based ink, packaging printing and the like, and is also suitable for offset printing, gravure printing and flexographic printing. Since these fields are in wide contact with consumers, if the purity of the permanent violet is not sufficient, some harmful impurities, especially polychlorinated biphenyl and arylamine, may exist to have adverse effects on consumers, and therefore, the measurement of the purity of the permanent violet is helpful for downstream users to better control the product quality.
Disclosure of Invention
Aiming at the defects in the prior art, the invention provides a convenient detection method.
The invention is realized by the following technical scheme:
a method for measuring the content of permanent violet is characterized in that a liquid chromatograph method is adopted for measurement, a diode array detector is adopted, and the detection conditions are as follows: the detection wavelength is 593 nanometers, the chromatographic column is a reversed phase C18 column, the mobile phase is tetrahydrofuran, the flow rate is 0.8-1.2 ml/min, the sample injection volume is 10-20 microliters, and the column temperature is 25-35 ℃.
Preferably, in the method for measuring the content of permanent violet, the chromatographic column has an inner diameter of 4.6 mm, a column length of 150 mm and a filler particle size of 5 microns.
Preferably, the flow rate in one of the aforementioned methods for measuring the content of permanent violet is 1.0 ml per minute.
The invention has the advantages that:
the method has the advantages that the content of the permanent violet is determined by adopting the liquid chromatography through groping and repeated test screening of specific determination conditions, the permanent violet is better separated from other organic impurities by selecting specific chromatographic columns and mobile phases, the reproducibility of the method is good, the scientificity, the advancement and the applicability of the determination method are provided, the determined content precision of the permanent violet is more accurate, and the method can be better used for a downstream user to check the purity of the permanent violet.
Drawings
FIG. 1 is a graph showing the results of example 1 of the present invention
Detailed Description
The following is a detailed description of the practice of the invention:
example 1
A method for measuring the content of permanent violet adopts liquid chromatography, and the detection conditions are as follows: the detection wavelength is 593 nm, the chromatographic column is a C18 column, the mobile phase is tetrahydrofuran, the flow rate is 0.8-1.2 ml per minute, the sample injection volume is 20 microliter, and the column temperature is 35 ℃. The results are shown in FIG. 1.
Example 2
A method for measuring the content of permanent violet adopts liquid chromatography, and the detection conditions are as follows: the detection wavelength is 593 nanometers, the chromatographic column is a C18 column, the mobile phase is tetrahydrofuran, the flow rate is 1.0 milliliter per minute, the sample injection volume is 15 microliters, the column temperature is respectively 25 ℃, wherein the inner diameter of the chromatographic column is 4.6 millimeters, the column length is 150 millimeters, and the filler particle size is 5 micrometers. The results were similar to those of example 1.

Claims (3)

1. A method for measuring the content of permanent violet is characterized in that a liquid chromatograph method is adopted for measurement, a diode array detector is adopted, and the detection conditions are as follows: the detection wavelength is 593 nm, the chromatographic column is a reversed phase C18 column, the mobile phase is tetrahydrofuran, the flow rate is 0.8-1.2 ml/min, and the sample injection volume
Figure FDA0002354626320000012
Microliter, column temperature of
Figure FDA0002354626320000011
2. The method for measuring content of permanent violet according to claim 1, wherein the chromatographic column has an inner diameter of 4.6 mm, a column length of 150 mm and a filler particle size of 5 microns.
3. The method of claim 1, wherein the flow rate is 1.0 ml per minute.
CN202010004216.0A 2020-01-03 2020-01-03 Content determination method of permanent violet Pending CN111141848A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010004216.0A CN111141848A (en) 2020-01-03 2020-01-03 Content determination method of permanent violet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010004216.0A CN111141848A (en) 2020-01-03 2020-01-03 Content determination method of permanent violet

Publications (1)

Publication Number Publication Date
CN111141848A true CN111141848A (en) 2020-05-12

Family

ID=70523396

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010004216.0A Pending CN111141848A (en) 2020-01-03 2020-01-03 Content determination method of permanent violet

Country Status (1)

Country Link
CN (1) CN111141848A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104245795A (en) * 2012-03-30 2014-12-24 沙特基础创新塑料Ip私人有限责任公司 Polyetherimides, methods of manufacture, and articles formed therefrom
CN109541059A (en) * 2018-11-19 2019-03-29 山西北化关铝化工有限公司 A method of measurement TCTNB purity

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104245795A (en) * 2012-03-30 2014-12-24 沙特基础创新塑料Ip私人有限责任公司 Polyetherimides, methods of manufacture, and articles formed therefrom
CN109541059A (en) * 2018-11-19 2019-03-29 山西北化关铝化工有限公司 A method of measurement TCTNB purity

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
刘俊等: "《可食性包装材料质量检验》", 30 April 2017, 中国质检出版社 *
张庆华等: ""永固紫"染料和四氯苯醌中多氯代二苯并二噁英/呋喃的分析", 《色谱》 *

Similar Documents

Publication Publication Date Title
Rafaëlly et al. Optimisation of ESI-MS detection for the HPLC of anthraquinone dyes
Pebdani et al. Solid phase microextraction of diclofenac using molecularly imprinted polymer sorbent in hollow fiber combined with fiber optic-linear array spectrophotometry
CN110108816A (en) The HS-GC/MS measuring method of 11 kinds of volatile hazardous substances in students' supplies
KR960034994A (en) Modification of colorimetric value
Cesaratto et al. A complete Raman study of common acid red dyes: application to the identification of artistic materials in polychrome prints
CA2423236A1 (en) Inks exhibiting expanded color-space characteristics for water-based printing
Campanella et al. Identification of inorganic dyeing mordant in textiles by surface-enhanced laser-induced breakdown spectroscopy
CN106770851B (en) A kind of mobile phase formula of liquid chromatography for measuring carotenoid and its application
Germinario et al. Pyrolysis gas chromatography–mass spectrometry of triarylmethane dyes
CN112946140A (en) Method for detecting water-soluble anion synthetic pigment in food
Sebastiano et al. Analysis of commercial Acid Black 194 and related dyes by micellar electrokinetic chromatography
Chiye et al. Extraction method and determination of Sudan I present in sunset yellow FCF by isocratic high-performance liquid chromatography
Akhmerova et al. Forensic identification of dyes in ballpoint pen inks using LC–ESI–MS
CN111141848A (en) Content determination method of permanent violet
Faraji et al. Application of vortex assisted dispersive liquid-liquid microextraction based on a new deep eutectic solvent for microextraction of aromatic amines from simulant of kitchenware samples by HPLC-UV
Casadio et al. Direct identification of early synthetic dyes: FT-Raman study of the illustrated broadside prints of José Gaudalupe Posada (1852–1913)
CN111307991B (en) Method for simultaneously detecting bromobenzene and carbazole compounds by adopting high performance liquid chromatography
Fremout et al. Characterization of daylight fluorescent pigments in contemporary artists’ paints by Raman spectroscopy
Śmigiel-Kamińska et al. Development of HPLC-DAD and UPLC-QTOF-MS chromatographic systems for the identification for forensic purposes of disperse dyes of polyester
CN113984910A (en) Detection and analysis method for determining aniline in soil
CN103558163A (en) Detection method for dye system polarizer dyeing solution composition concentration change
JP2006329641A (en) Analyzing method of solvent soluble coloring matter
DE102006048638A1 (en) New perylene dyes e.g. useful as pigments in inks, paints, lacquers and plastics
CN111138313B (en) Schiff base compound with aggregation-induced emission characteristic and method for preparing ratiometric fluorescent probe by using Schiff base compound
Lewandowska et al. A preliminary study for the fast prototyping of simple electroplanar separation systems based on various natural polymers and planar chromatographic stationary phases

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20200512