A kind of preparation method of PT catalyst
A technology of catalysts and compounds, applied in catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of difficult interface guarantee and control.
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[0029] The present invention provides a method for preparing a Pt catalyst, which includes the following steps:
[0030] a) Mixing the carbon carrier, the Pt precursor, the titanium precursor, the regulator, and ethanol to obtain a mixed suspension, the regulator including an organic acid compound or an organic base compound;
[0031] b) irradiating the mixed suspension obtained in step a) with ultraviolet light to obtain a Pt catalyst.
[0032] The preparation method provided by the invention uses light to excite the titanium precursor to hydrolyze in situ to obtain TiO 2 The electrons generated at this time are used as reducing agents, and the electrons are used as Pt precursors to reduce the Pt atoms generated in situ. Compared with the prior art, the present invention uses the electrons generated in situ from the titanium precursors as the reducing agent. Control the hydrolysis reaction of the titanium precursor, thereby controlling the amount of subsequent photo-excited electron...
Embodiment 1
[0055] Add 112.6 mg of activated carbon produced by Cabot Company in the United States under the trade name of Vulcan XC-72R to 150 mL of absolute ethanol, disperse ultrasonically for 0.5 h, and then pass N into the activated carbon suspension 2 Deoxygenate the gas for 30 minutes; add 8mL of 3.7mol / L chloroplatinic acid aqueous solution and triethylamine to the above-mentioned deoxygenated suspension, n(triethylamine): n(chloroplatinic acid)=3, After stirring for 30 minutes, add 280 μL of isopropyl titanate, and put it under UV light for 24 hours;
[0056] Use deionized water with a resistivity of 18.2MΩ·cm to filter and wash the suspension until there is no Cl - , The obtained solid material was vacuum dried at 80° C. to obtain a platinum catalyst, and the sample was marked as sample-1.
[0057] The platinum content of the platinum catalyst prepared in Example 1 of the present invention is 13.8 wt%.
[0058] The present invention performs X-ray diffraction analysis on the Pt catalys...
Embodiment 2
[0062] This embodiment adopts the same preparation method as in embodiment 1, except that the amount of triethylamine added: n (triethylamine): n (chloroplatinic acid)=2.
[0063] The test method and experimental conditions of this example are the same as those of Example 1, and the catalyst prepared in Example 2 is marked as sample-2.
[0064] The present invention performs X-ray diffraction analysis on the Pt catalyst obtained in Example 2 according to the above technical scheme, and the test results are shown in figure 1 , figure 1 These are the X-ray diffraction (XRD) graphs of the Pt catalyst prepared in Examples 1 to 6 of the present invention and the comparative example, where curve 2 is the X-ray diffraction (XRD) curve of the Pt catalyst prepared in Example 2 of the present invention;
[0065] The present invention carries out cyclic voltammetry test on the Pt catalyst prepared in Example 2 according to the above technical scheme, and the test results are as follows image 3 ...
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Abstract
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