Trimellitic acid-ltbh complex and its synthesis method
A technology of trimesic acid and trimesic acid sodium salt is applied in the field of trimesic acid-LTbH complex and its synthesis, which can solve the problems of affecting luminous intensity, fluorescence quenching, inability to meet requirements, etc., so as to improve luminescence performance effect
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Embodiment 1
[0041] (1), using the uniform precipitation method to synthesize NO 3 -LTbH precursor
[0042] 0.453g (1mmol) Tb (NO 3 ) 3 ·6H 2 O, 1.10g (13mmol) NaNO 3 , 0.14g (1mmol) of hexamethylenetetramine (HMT) was dissolved in 80ml of degassed water to obtain an aqueous solution, and then hydrothermally reacted at 70°C for 16 hours. After the reaction, the obtained product was filtered by suction, washed with deionized water, and then filtered by suction, repeated 3 times, and dried in vacuum for 24 hours to obtain white powdery NO 3 - LTbH 0.251 g. to NO 3 Based on -LTbH, the yield was 96%.
[0043] (2), using ion exchange method to synthesize terephthalic acid-LTbH complex
[0044]0.166 g (1 mmol) of terephthalic acid and 0.060 g (1.5 mmol) of NaOH were added into 5 mL of deionized water to dissolve them completely to obtain a clear aqueous solution of sodium terephthalate salt.
[0045] 0.033g NO 3 -LTbH was dispersed in 75ml of deionized water, mixed with the above-prepa...
Embodiment 2
[0050] (1), using the uniform precipitation method to synthesize NO 3 -LTbH precursor
[0051] 0.453g (1mmol) Tb (NO 3 ) 3 ·6H 2 O, 1.650g (19.5mmol) NaNO 3 , 0.21g (1.5mmol) of hexamethylenetetramine was dissolved in 120ml of degassed water to obtain an aqueous solution, and then hydrothermally reacted at 90°C for 12 hours. After the reaction, the obtained product was filtered by suction, washed with deionized water and then filtered by suction, repeated 3 times, and then vacuum-dried for 24 hours to obtain white powdery NO 3 -LTbH 0.257g. to NO 3 Based on -LTbH, the yield was 98%.
[0052] (2), using ion exchange method to synthesize terephthalic acid-LTbH complex
[0053] 0.166 g (1 mmol) of terephthalic acid and 0.080 g (2 mmol) of NaOH were added into 5 mL of deionized water to dissolve them completely to obtain a clear aqueous solution of sodium terephthalate salt.
[0054] 0.087g NO 3 -LTbH was dispersed in 100 ml of deionized water, mixed with the aqueous sol...
Embodiment 3
[0059] (1), using the uniform precipitation method to synthesize NO 3 -LTbH precursor
[0060] 0.453g (1mmol) Tb (NO 3 ) 3 ·6H 2 O, 2.20g (26mmol) NaNO 3 , 0.28g (2mmol) of hexamethylenetetramine was dissolved in 160ml of degassed water to obtain an aqueous solution, which was hydrothermally reacted at 100°C for 18 hours. After the reaction, the obtained product was filtered by suction, washed with deionized water, and then filtered by suction, repeated 3 times, and dried in vacuum for 24 hours to obtain white powdery NO 3 - LTbH 0.258 g. to NO 3 Based on -LTbH, the yield was (98.8%).
[0061] (2), using ion exchange method to synthesize terephthalic acid-LTbH complex
[0062] 0.166 g (1 mmol) of terephthalic acid and 0.072 g (1.8 mmol) of NaOH were added into 5 mL of deionized water to dissolve them completely to obtain a clear aqueous solution of sodium terephthalate salt.
[0063] 0.118g NO 3 -LTbH was dispersed in 150 ml of deionized water, mixed with the aqueous...
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