Sulfonated cyanine dyes/hydrotalcite composite film and preparation method thereof
A technology of sulfonated cyanine and composite film, applied in chemical instruments and methods, organic dyes, methine/polymethine dyes, etc., can solve the problems of near-infrared absorption and fluorescent films that have not been reported, and achieve the purpose of inhibiting aggregation Generate, enhance photothermal stability, and improve photothermal stability
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Embodiment 1
[0023] 1. Preparation of nitrate hydrotalcite precursor by co-precipitation method:
[0024] a. 0.015mol solid Mg(NO 3 ) 3 ·6H 2 O and 0.0075mol of solid Al(NO 3 ) 3 9H 2 O dissolved in 100mL to remove CO 2 of deionized water;
[0025] b. Dissolve 0.0625mol NaOH in 100mL to remove CO 3 of deionized water;
[0026] c. the alkali solution prepared by step b is placed in a four-necked bottle, 2 Stir vigorously under the condition of air protection, and at the same time slowly add the salt solution prepared in step a into the four-necked bottle for about 0.5h. After the addition is completed, adjust the pH value to 8 with 1mol / L NaOH solution. , 60 ℃ water bath reaction for 24h, with CO removal 3 The deionized hot water was centrifuged and washed to a pH of about 7, and dried at 50°C for 24 hours to obtain a magnesium-aluminum nitrate hydrotalcite precursor;
[0027] 2. Take 0.1 g of the magnesium-aluminum nitrate hydrotalcite precursor prepared in step 1 and stir in 10...
Embodiment 2
[0033] 1. Preparation of nitrate hydrotalcite precursor by ion exchange method:
[0034] a. Add 0.01mol of solid Mg(NO 3 ) 3 ·6H 2 O and 0.005 mol of solid Al(NO 3 ) 3 9H 2 O and 0.06mol urea were dissolved in 50mL of deionized water, in a 90ml polytetrafluoroethylene pressure reaction vessel, crystallized at 100°C for 24 hours, and washed by centrifugation with deionized water until the pH was about 7, 50 Dry at ℃ for 24 hours to obtain carbonate intercalated hydrotalcite powder;
[0035] b. Take 0.3 g of the above-mentioned carbonate intercalation hydrotalcite powder and solid NaNO 363.75g dissolved in 300mL to remove CO 2 After uniformly dispersed in deionized water, add 0.09mL of concentrated nitric acid and stir at 20°C under a nitrogen atmosphere to carry out ion exchange reaction for 18 hours and then use 2 The deionized hot water was centrifuged and washed to a pH of about 7, and vacuum-dried at 50°C for 18 hours to obtain a magnesium-aluminum nitrate hydrotalc...
Embodiment 3
[0042] 1. Preparation of nitrate hydrotalcite precursor by co-precipitation method:
[0043] a. 0.02mol solid Zn(NO 3 ) 2 ·6H 2 O and 0.01mol of solid Al(NO 3 ) 3 9H 2 O dissolved in 100mL to remove CO 2 of deionized water;
[0044] b. Dissolve 0.08mol NaOH in 100mL to remove CO 2 of deionized water;
[0045] c. the alkali solution prepared by step b is placed in a four-necked bottle, 2 Stir vigorously under the condition of air protection, and at the same time slowly add the salt solution prepared in step a into the four-necked bottle for about 0.5h. After the addition is completed, adjust the pH value to 8 with 1mol / L NaOH solution. , 60 ℃ water bath reaction for 24h, with CO removal 2 The deionized hot water was centrifuged and washed to a pH of about 7, and dried at 50°C for 24 hours to obtain a zinc-aluminum nitrate hydrotalcite precursor;
[0046] 2. Take 0.13 g of the zinc-aluminum nitrate hydrotalcite precursor prepared in step 1 and stir in 100 ml of formam...
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