Method for detecting cyanolabe in textiles by reversed phase high performance liquid chromatography
A reversed-phase high-performance liquid chromatography and chromatographic detection technology, which is applied in the field of reversed-phase high-performance liquid chromatography to detect blue pigments in textiles, can solve problems such as differences in the applicability of carcinogenic aromatic amines, uncertain conversion rates, and difficult judgments, and achieve linearity The effect of good relationship, ensuring accuracy, and high extraction separation effect
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Embodiment 1
[0078] 1 Experimental instruments and reagents
[0079] 1.1 Experimental Instruments
[0080] Shimadzu LC-10AT high performance liquid chromatography, Kromsil ODS-1 C18, 5μ, 250mm×4.6mm chromatographic column; SPD-10A ultraviolet detector, SCL-10A recorder, KQ-500DE numerical control ultrasonic cleaner, electric heating Blast drying oven. FINNIGAN LCQ DECA XP MAX liquid mass spectrometer.
[0081] 1.2 Drugs and reagents
[0082] Acetonitrile Chromatographically pure
[0083] Methanol Chromatographically pure
[0084] Ethanol Chromatographically pure
[0085] Potassium dihydrogen phosphate analytically pure Tianjin Beilian Fine Chemicals Development Co., Ltd.
[0086] Sodium hydroxide Analytical grade Guangzhou Chemical Reagent Factory
[0087] Triethylamine analytically pure
[0088] Phosphoric acid analytically pure
[0089] C 39 h 23 ClCrN 7 o 12S.2Na standard sample (purity 93%).
[0090] 2 sample preparation
[0091] 2.1 Extraction sample preparation:
[00...
Embodiment 2
[0115] The difference from Example 1 is:
[0116] Standard curve: Measure 0.201mg / ml, 0.100mg / ml, 0.080mg / ml, 0.060mg / ml, 0.040mg / ml and 0.020mg / ml standard solutions prepared in 2.2 of Example 1 and inject 20μl each into the liquid chromatograph Instrument, according to the above method configuration standard solution was measured by reversed-phase high-performance liquid chromatography, and the peak area was measured at 254nm wavelength. With the concentration as the abscissa and the peak area as the ordinate, draw a standard curve ( Figure 6 ).
[0117] The resulting regression equation is:
[0118] (2) Y=aX+b, (a=3.703613e-008, b=2.870155e-003), R=0.9996135
[0119] Determination of blue pigment content in the sample to be tested: take the actual sample prepared in 2.1, and carry out high-performance liquid chromatography determination with the chromatographic conditions of 3.1: the peak area is 1405145, select the standard curve (2), and the measured concentration of ...
Embodiment 3
[0121] 1 Experimental instruments and reagents are the same as in Example 1
[0122] 2 Sample preparation
[0123] 2.1 Extraction sample preparation:
[0124] A single dyed textile sample was cut into small pieces of 3.5 cm x 3.5 cm. The weighed weight was 0.5562g. Place the sample in a 50mL colorimetric tube, add 15mL of methanol:water=80:20 mixed solution, place in an ultrasonic bath with a frequency of 450W, and extract at (70±2)°C for 30min. The extract was cooled at room temperature and filtered through a polytetrafluoroethylene membrane filter with a pore size of 0.45 μm. Avoid excessive contact with other plastic polymers when filtering. Pour the extract into a 1mL sample bottle, tighten the Teflon cap, and save it for later use.
[0125] 2.2 Standard sample preparation is the same as in Example 1
[0126] 2.3 Mobile phase equipment:
[0127] Potassium dihydrogen phosphate and potassium phosphate mixed solution: Weigh 2.60 grams of potassium dihydrogen phosphate ...
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