BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING
FIGS. 1A and 1B show schematic explanatory drawings of a fluorescent lamp according to the invention;
FIGS. 2A and 2B show conceptual explanatory drawings of a deodorization unit according to the invention;
FIG. 3 shows X-ray diffraction data of monoclinic crystal system WO3 which is a main component of the photocatalyst powder of the invention;
FIG. 4 shows X-ray diffraction patterns of triclinic crystal system and monoclinic crystal system of tungsten trioxide (WO3);
FIG. 5 shows a characteristic drawing showing the comparison of acetaldehyde decomposition effects in the case where the crystal structures of tungsten trioxide differ;
FIG. 6 shows a conceptual drawing of a measurement apparatus employed for obtaining the characteristic drawing of FIG. 5;
FIG. 7 shows a conceptual drawing of a production apparatus for producing the photocatalytic material of the invention;
FIG. 8 shows a graph of particle size distribution (the relation among frequency, the particle diameter and the integrated penetration) after dispersion;
FIG. 9 shows a graph of particle size distribution (the relation among frequency, the particle diameter and the integrated penetration) of the WO3-dispersed coating material;
FIG. 10 shows a microscopic photograph of ammonium meta-tungstate as a granular raw material obtained in a third embodiment;
FIG. 11 shows a microscopic photograph of monoclinic crystal system type WO3 crystal photocatalyst fine particles obtained by rapid and short time heating of the granular raw material obtained in the third embodiment at 800° C. for 1 to 10 minutes;
FIG. 12 shows a characteristic drawing showing the acetaldehyde decomposition capability of the respective tungsten trioxide photocatalyst fine particles obtained by firing at a temperature of 600° C., 700° C., 800° C., and 900° C. in a fourth embodiment;
FIG. 13 shows a characteristic drawing showing the acetaldehyde decomposition capability of the respective tungsten trioxide photocatalyst fine particles obtained by firing at a temperature of 600° C., 700° C., 800° C., and 900° C. in the fourth embodiment;
FIG. 14 shows a characteristic drawing showing the acetaldehyde decomposition capability in the case where the firing time is changed to be 30 seconds, 1 minute, 5 minutes, 10 minutes, and 15 minutes;
FIG. 15 shows a drawing showing the relation between the wavelength and the reflectivity in the case of using WO3 photocatalyst of a sixth embodiment and TiO2 photocatalyst;
FIG. 16 shows a perspective view in the disassembled state of the lighting apparatus according to the sixth embodiment;
FIG. 17 shows an enlarged cross-sectional drawing of the main part of FIG. 16; and
FIG. 18 shows the relation between the time and the acetaldehyde remaining ratio by using the lighting apparatus of a seventh embodiment in combination with a TiO2 photocatalyst-bearing fluorescent lamp, the TiO2 photocatalyst-bearing fluorescent lamp, and a TiO2 photocatalyst-bearing lighting apparatus in combination with the TiO2 photocatalyst-bearing fluorescent lamp.