scholarly journals Improving Carbon-Coated TiO2 Films with a TiCl4 Treatment for Photocatalytic Water Purification

ChemCatChem ◽  
2017 ◽  
Vol 10 (1) ◽  
pp. 234-243 ◽  
Author(s):  
Gylen Odling ◽  
Aruna Ivaturi ◽  
Efthalia Chatzisymeon ◽  
Neil Robertson
Keyword(s):  
Water Purification ◽  
Tio2 Films ◽  
Ticl4 Treatment ◽  
Carbon Coated

scholarly journals Carbon modified TiO2 photocatalysts for water purification

2009 ◽  
Vol 11 (2) ◽  
pp. 46-50 ◽  
Author(s):  
Antoni Morawski ◽  
Magdalena Janus ◽  
Beata Tryba ◽  
Masahiro Toyoda ◽  
Tomoki Tsumura ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Water Purification ◽  
Visible Region ◽  
Carbon Layer ◽  
Photocatalytic Decomposition ◽  
Visible Range ◽  
Tio2 Photocatalysts ◽  
Carbon Doped ◽  
Carbon Coated

Carbon modified TiO2 photocatalysts for water purification Carbon can form different structures with TiO2: carbon-doped TiO2, carbon coated TiO2 and composites of TiO2 and carbon. The presence of carbon layer on the surface of TiO2 as well as the presence of porous carbon in the composites with TiO2 can increase the concentration of organic pollutants on the surface of TiO2, facilitating the contact of the reactive species with the organic molecules. Carbon-doped TiO2 can extend the absorption of the light to the visible region by the narrowing of the band gap and makes the photocatalysts active under visible light irradiation. TiO2 loaded carbon can also work as a photocatalyst, on which the molecules are adsorbed in the pores of carbon and then they undergo the photocatalytic decomposition with UV irradiation. Enhanced photocatalytic activity for the destruction of some organic compounds in water was noticed on the carbon coated TiO2 and TiO2 loaded activated carbon, mostly because of the adsorptive role of carbon. However, in carbon-doped TiO2, the role of carbon is somewhat different, the replacement of carbon atom with Ti or oxygen and formation of oxygen vacancies are responsible for extending its photocatalytic activity towards the visible range.

Biophysical Measurement of Molecular Weight of Foot-and-Mouth Disease RNA Fragments

1974 ◽  
Vol 32 ◽  
pp. 262-263
Author(s):  
Sydney S. Breese ◽  
Howard L. Bachrach
Keyword(s):  
Chemical Properties ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Distilled Water ◽  
Bovine Plasma ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Carbon Coated ◽  
Rna Fragments ◽  
Physical And Chemical

Continuing studies on the physical and chemical properties of foot-and-mouth disease virus (FMDV) have included electron microscopy of RNA strands released when highly purified virus (1) was dialyzed against demlneralized distilled water. The RNA strands were dried on formvar-carbon coated electron microscope screens pretreated with 0.1% bovine plasma albumin in distilled water. At this low salt concentration the RNA strands were extended and were stained with 1% phosphotungstic acid. Random dispersions of strands were recorded on electron micrographs, enlarged to 30,000 or 40,000 X and the lengths measured with a map-measuring wheel. Figure 1 is a typical micrograph and Fig. 2 shows the distributions of strand lengths for the three major types of FMDV (A119 of 6/9/72; C3-Rezende of 1/5/73; and O1-Brugge of 8/24/73.

The Application of Ultracryotomy to Immunocytochemistry

1973 ◽  
Vol 31 ◽  
pp. 704-709
Author(s):  
R. G. Painter ◽  
K. T. Tokuyasu ◽  
S. J. Singer
Keyword(s):  
Frozen Sections ◽  
Protein Antigens ◽  
Carbon Coated ◽  
Antibody Conjugates ◽  
Ultrathin Frozen Sections

A technique for localizing intracellular antigens with immunoferritin conjugates directly on ultrathin frozen sections of glutaraldehyde-fixed tissues has been developed. This method overcomes some of the limitations of previously described procedures, since it avoids drastic fixation, dehydration and embedding procedures which could denature many protein antigens.Briefly cells or tissues were fixed with glutaraldehyde (0.5 to 2% for 1 hr), and ultrathin frozen sections were cut and mounted on grids covered with carbon-coated Formvar film by the procedure described previously. Such sections were stained with ferritin-antibody conjugates by methods described elsewhere.

Ultrastructural Alterations in Hela Cells Induced by Spider Venom

1967 ◽  
Vol 25 ◽  
pp. 20-21
Author(s):  
Dale E. McClendon ◽  
Paul N. Morgan ◽  
Bernard L. Soloff
Keyword(s):  
Growth Medium ◽  
Mammalian Cells ◽  
Carcinoma Cells ◽  
Venom Protein ◽  
Sterile Saline ◽  
Carbon Coated ◽  
Available Information ◽  
Loxosceles Reclusa ◽  
Essential Growth ◽  
Solution Cultures

It has been observed that minute amounts of venom from the brown recluse spider, Loxosceles reclusa, are capable of producing cytotoxic changes in cultures of certain mammalian cells (Morgan and Felton, 1965). Since there is little available information concerning the effect of venoms on susceptible cells, we have attempted to characterize, at the electron microscope level, the cytotoxic changes produced by the venom of this spider.Cultures of human epithelial carcinoma cells, strain HeLa, were initiated on sterile, carbon coated coverslips contained in Leighton tubes. Each culture was seeded with approximately 1x105 cells contained in 1.5 ml of a modified Eagle's minimum essential growth medium prepared in Hank's balanced salt solution. Cultures were incubated at 36° C. for three days prior to the addition of venom. The venom was collected from female brown recluse spiders and diluted in sterile saline. Protein determinations on the venom-were made according to the spectrophotometric method of Waddell (1956). Approximately 10 μg venom protein per ml of fresh medium was added to each culture after discarding the old growth medium. Control cultures were treated similarly, except that no venom was added. All cultures were reincubated at 36° C.

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