Magnetic hydroxyl nano material Fe3O4 (at) COFs and application thereof in field of sulfanilamide mass spectrometry detection
A nanomaterial and hydroxyl technology, which is applied in the preparation of sulfonamide matrix-assisted laser desorption ionization mass spectrometry detection probes and the field of magnetic hydroxyl organic framework nanomaterials, achieves the advantages of good enrichment and ionization, good reproducibility, and good salt tolerance. Effect
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Embodiment 1
[0030] Example 1 Fe 3 o 4 Synthesis of @COFs
[0031] Take Fe respectively 3 o 4 (100mg, synthesized according to existing literature reports), TAPB (0.04mmol) and DHTP (0.06mmol) were put into a 50mL single-necked bottle, and then 5mL of acetonitrile was added. In order to fully mix and disperse the above substances, the above mixture was sonicated for 1min; then 0.4mL Acetic acid (12M), shake the mixture well, and react at room temperature for 72h; collect the brownish-yellow solid obtained, wash by 25mL methanol, and centrifuge at 8000rpm / min for 10 minutes, wash and centrifuge three times, and vacuum-dry overnight at room temperature , that is.
Embodiment 2
[0032] Example 2 Fe 3 o 4 Synthesis of @COFs
[0033] Take Fe respectively 3 o 4 (75mg, synthesized according to existing literature reports), TAPB (0.04mmol) and DHTP (0.06mmol) were put into a 50mL single-necked bottle, and then 5mL of acetonitrile was added. In order to fully mix and disperse the above substances, the above mixture was sonicated for 1min; then 0.4mL Acetic acid (12M), shake the mixture well, and react at room temperature for 72h; collect the brownish-yellow solid obtained, wash by 25mL methanol, and centrifuge at 8000rpm / min for 10 minutes, wash and centrifuge three times, and vacuum-dry overnight at room temperature , that is.
Embodiment 3
[0034] Example 3 Fe 3 o 4 Synthesis of @COFs
[0035] Take Fe respectively 3 o 4 (50mg, synthesized according to existing literature reports), TAPB (0.04mmol) and DHTP (0.06mmol) were put into a 50mL single-necked bottle, and then 5mL of acetonitrile was added. In order to fully mix and disperse the above substances, the above mixture was sonicated for 1min; then 0.4mL Acetic acid (12M), shake the mixture well, and react at room temperature for 72h; collect the brownish-yellow solid obtained, wash by 25mL methanol, and centrifuge at 8000rpm / min for 10 minutes, wash and centrifuge three times, and vacuum-dry overnight at room temperature , that is.
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