Titania photocatalytic compounds and methods of making the same
A technology of titanium oxide and compounds, applied in the field of chemistry, can solve problems such as not being suitable for improving the photocatalytic activity of titanium dioxide
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Embodiment 1
[0085] Embodiment 1: the synthesis of compound A
[0086] A 50% by weight aqueous solution of TYZOR LA (25 mL, Sigma Aldrich, St. Louis, MO, SA) was preheated in a furnace (Barnstead Thermolyne 47900, Dubuque, IA, USA) to 350 °C for about 20 to 30 minutes to burn And formed a large amount of black powder. After gas was no longer observed, the resulting powder was transferred without crushing into a large glass Petri dish (100 x 50), heated to 475°C and held at this temperature for about 1 hour. Next, the above Petri dish was cooled to room temperature to yield a pale yellow powder. The pale yellow powder (compound A) was manually pulverized using a pestle and mortar for characterization and photocatalytic evaluation.
Embodiment 2
[0087] Embodiment 2: the synthesis of compound B, C and D
[0088] Comparative compound A (P25 Titania) was obtained from Evonik (Evonik Degussa Corp., Parsippany, NJ, USA). Compound B, Compound C, and Compound D were prepared in a similar manner to Example 1, except that the amount of TYZOR LA was varied and additional precursor was added to TYZOR LA prior to combustion, as shown in Table 1 below:
[0089] Table 1: Precursor materials of the compounds of Example 1 and Example 2
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[0091] *Comparative compound A is Titania P25 from Evonik.
Embodiment 3
[0092] Embodiment 3: the synthesis of compound E to AB
[0093] Compounds E to AD were prepared in a similar manner to Example 1, except that the amount of TYZOR LA was varied and additional precursors were added prior to combustion as shown in Table 2 below. For compounds AC and AD, noble metal compounds were included as additional precursors to obtain catalytic compositions with noble metals.
[0094] Table 2: Precursor materials for the compounds of Example 1 and Example 2
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