Method for detecting Sudan red I in aqueous phase, fluorescence test paper and preparation method and application thereof
A technology for detecting Sudan red and water, which is applied in the fields of optics and polymer chemistry, can solve problems such as increasing the cost of detection, restricting detection of Sudan Red I, etc., and achieves the effects of improved sensitivity, good water solubility, and simple and easy preparation process
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Embodiment 1
[0039] 5g of purified chitosan (Mw=50000) was added to 50mL of saturated NaOH solution with a mass fraction of 50%, stirred evenly and placed in the refrigerator overnight; the swollen sample was transferred to a 1000mL beaker, and 300mL of iso Propanol was stirred evenly; 5g of chloroacetic acid was added to the beaker in batches, and mechanically stirred for 12 hours; the isopropanol was filtered out, and water was added to dissolve the sample; the pH of the solution was adjusted to neutral with dilute acetic acid, and dialyzed in deionized water for 3-5d (MWCO= 3500); the solution in the dialysis bag was collected and freeze-dried for 48 hours to obtain CMCs; 10g of ionic liquid [Bmim]Cl was heated and melted, and 0.2g of dry CMCs was added, N 2 Under the protection of 1500rmp magnetic stirring for 3h to completely dissolve the CMCs; N 2 Add 0.388g p-dioxanone (PDO) and 0.128g 4-dimethylaminopyridine (DMAP) to the solution under protection, N 2 Under protection, react at 1...
Embodiment 2
[0041] The CMCs-g-PPDO prepared in Example 1 was formulated into a 0.9 mg / mL aqueous solution of polymer nanomicelles, and 1 mL of a 0.5 mg / mL PFO / THF solution was slowly added dropwise to 10 mL of an aqueous solution of polymer nanomicelles with stirring. Ultrasound for 2 hours to mix evenly, remove THF by rotary evaporation, add water to 10mL; filter with 0.45 μm microporous membrane to remove unembedded PFO to obtain the amphiphilic chitosan derivative CMCs-g-PPDO / PFO nanocomposite Fluorescent probe solution. The loading rate of the conjugated polymer PFO in the probe solution was measured and calculated by an ultraviolet spectrometer to be 11.36%; 2.5 mL of the probe solution diluted 5 times was placed in a four-sided quartz cuvette, and at an excitation wavelength of 340 nm, a narrow Scan the fluorescence spectrum under the condition of a slit width of 2.5nm; drop 10 μL of the sample solution to be tested into the cuvette containing the fluorescent probe solution, scan it...
Embodiment 3
[0043] The CMCs-g-PPDO prepared in Example 1 was formulated into a 1.35 mg / mL aqueous solution of polymer nanomicelles, and the particle size was determined to be 23.18 nm by dynamic light scattering (DLS) using a Malvern particle size analyzer; 100 μL 0.5 mg / mL PFO / THF solution was slowly added dropwise to 10mL polymer nanomicelle aqueous solution under stirring condition, ultrasonically mixed for 2h, then rotary evaporated to remove THF, added water to make up to 10mL; filtered with 0.45μm microporous membrane to remove unembedded PFO That is, the amphiphilic chitosan derivative CMCs-g-PPDO / PFO nanocomposite fluorescent probe solution is obtained. The loading rate of the conjugated polymer PFO in the probe solution was measured and calculated by an ultraviolet spectrometer to be 41.94%; 2.5 mL of the probe solution diluted 5 times was placed in a four-sided quartz cuvette, and the excitation wavelength was 340 nm, narrowly Scan the fluorescence spectrum under the condition o...
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