Preparation of a triptycene polymer NTP/ zinc cadmium sulfide Cd0.5Zn0.5S composite photocatalyst

A technology of zinc cadmium sulfide and triptycene, applied in organic compound/hydride/coordination complex catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problem that the photocatalytic hydrogen production activity has not been thoroughly studied, etc. The problem is that the preparation conditions are easy to control, the catalytic efficiency is high, and the preparation method is simple.

Active Publication Date: 2018-04-06
CHANGZHOU UNIV
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Problems solved by technology

[0004] Literature survey found that NTP-Cd 0.5 Zn 0.5 The photocatalytic hydrogen production activity of S nanocomposites has not been thoroughly investigated

Method used

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  • Preparation of a triptycene polymer NTP/ zinc cadmium sulfide Cd0.5Zn0.5S composite photocatalyst
  • Preparation of a triptycene polymer NTP/ zinc cadmium sulfide Cd0.5Zn0.5S composite photocatalyst
  • Preparation of a triptycene polymer NTP/ zinc cadmium sulfide Cd0.5Zn0.5S composite photocatalyst

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Experimental program
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Embodiment 1

[0031] (1)Cd 0.5 Zn 0.5 Preparation of S

[0032] Na 2 S (1.5608g, 20mmol) was dissolved in 40mL deionized water, and Cd(OAc) was added 2 2H 2 O (2.305g, 10mmol) and Zn(OAc) 2 2H 2 O (1.8348 g, 10 mmol) in 40 mL of an aqueous solution was stirred at room temperature for 24 hours. Then, the product was filtered, washed several times with deionized water, and dried in an oven at 80 °C for 5 h.

[0033] (2) Preparation of NTP

[0034] a: Place triptene (1.25g, 5mmol) in a three-necked flask, add concentrated HNO 3 50 mL, the mixture was heated and stirred at 75° C. for 24 h, and condensed under reflux. The reaction solution was a brown solution, which was cooled to room temperature, then poured into H 2 O (1000 mL) was stirred for 30 min. The precipitate was collected, washed with distilled water, and dried in air. The crude product was purified with dichloromethane / petroleum ether (1:1) as the eluent to give the white solid products 2,6,14-trinitrotriptene (2a) and ...

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Abstract

The invention relates to a preparation of a triptycene polymer NTP / zinc cadmium sulfide Cd0.5Zn0.5S composite photocatalyst. The method comprises the following steps: preparing a triptycene polymer NTP, preparing zinc cadmium sulfide Cd0.5Zn0.5S and preparing the triptycene polymer NTP doped zinc sulfide cadmium (NTP@Cd0.5Zn0.5S) composite photocatalyst. The preparation method provided by the invention has the beneficial effects that the preparation method is simple, the preparation conditions are easy to control, and the prepared triptycene polymer NTP doped zinc sulfide cadmium Cd0.5Zn0.5Scomposite catalyst has the advantages of no secondary pollution and high photocatalytic efficiency and the like, and has a certain application value.

Description

technical field [0001] The invention belongs to the technical field of preparation and application of nanomaterials, and relates to a method for preparing tripterene polymer NTP / zinc cadmium sulfide Cd 0.5 Zn 0.5 The preparation method of the S composite photocatalyst also belongs to the field of organic chemical synthesis. Background technique [0002] Organic microporous polymers have attracted widespread attention in recent years and become one of the current research hotspots. They not only have a beautiful molecular structure, but also have the advantages of ultra-high specific surface area, tunable pore properties, and easy modification of functional groups, which make this material have potential application prospects in the fields of gas storage, biomedicine, and homogeneous heterogeneous catalysis. Scientists regard designing and synthesizing new multifunctional materials, enriching synthetic methods of organic chemistry, and exploring the structure-activity relat...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J31/26C01B3/04
CPCB01J31/26B01J35/004C01B3/042C01B2203/0277C01B2203/1076Y02E60/36
Inventor 梁倩崔赛楠李忠玉
Owner CHANGZHOU UNIV
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