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2025-08-14 20:51
2960
The first commercial production of TiO2 began in the early 20th century, using the sulfate process. This method involved reacting ilmenite ore with sulfuric acid to produce titanium sulfate, which was then calcined to obtain titanium dioxide. However, this process had several drawbacks, including high energy consumption, generation of large amounts of waste, and release of harmful gases such as sulfur dioxide. As a result, many factories transitioned to the chloride process, which offers higher purity TiO2 and reduced environmental impact.
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2025-08-14 20:49
1658
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2025-08-14 20:23
2745
trans-5-Octenal
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2025-08-14 20:08
913
Different dermal cell types have been reported to differ in their sensitivity to nano-sized TiO2 . Kiss et al. exposed human keratinocytes (HaCaT), human dermal fibroblast cells, sebaceous gland cells (SZ95) and primary human melanocytes to 9 nm-sized TiO2 particles at concentrations from 0.15 to 15 μg/cm2 for up to 4 days. The particles were detected in the cytoplasm and perinuclear region in fibroblasts and melanocytes, but not in kerati-nocytes or sebaceous cells. The uptake was associated with an increase in the intracellular Ca2+ concentration. A dose- and time-dependent decrease in cell proliferation was evident in all cell types, whereas in fibroblasts an increase in cell death via apoptosis has also been observed. Anatase TiO2 in 20–100 nm-sized form has been shown to be cytotoxic in mouse L929 fibroblasts. The decrease in cell viability was associated with an increase in the production of ROS and the depletion of glutathione. The particles were internalized and detected within lysosomes. In human keratinocytes exposed for 24 h to non-illuminated, 7 nm-sized anatase TiO2, a cluster analysis of the gene expression revealed that genes involved in the “inflammatory response” and “cell adhesion”, but not those involved in “oxidative stress” and “apoptosis”, were up-regulated. The results suggest that non-illuminated TiO2 particles have no significant impact on ROS-associated oxidative damage, but affect the cell-matrix adhesion in keratinocytes in extracellular matrix remodelling. In human keratinocytes, Kocbek et al. investigated the adverse effects of 25 nm-sized anatase TiO2 (5 and 10 μg/ml) after 3 months of exposure and found no changes in the cell growth and morphology, mitochondrial function and cell cycle distribution. The only change was a larger number of nanotubular intracellular connections in TiO2-exposed cells compared to non-exposed cells. Although the authors proposed that this change may indicate a cellular transformation, the significance of this finding is not clear. On the other hand, Dunford et al. studied the genotoxicity of UV-irradiated TiO2 extracted from sunscreen lotions, and reported severe damage to plasmid and nuclear DNA in human fibroblasts. Manitol (antioxidant) prevented DNA damage, implying that the genotoxicity was mediated by ROS.
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2025-08-14 19:58
1555
Well asides from making you re-think that M & M addiction (chocolate coated in Titanium Dioxide…..anyone?!)
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2025-08-14 19:52
1091
Should I be worried about the use of titanium dioxide in my toothpaste?
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2025-08-14 19:28
643
The photocatalytic properties of rutile titanium dioxide make it an important material in environmental applications
titanium oxide rutile. When exposed to ultraviolet light, it can catalyze reactions that break down organic pollutants into carbon dioxide and water, thereby helping to purify air and water. This feature is utilized in self-cleaning surfaces, air purification systems, and even in the development of certain antimicrobial products.
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2025-08-14 19:13
2384
In a paints factory, anatase titanium dioxide plays a crucial role in determining the quality of the final product. The pigment is added to various types of paints, including water-based paints, oil-based paints, and powder coatings, to improve their performance and appearance. Anatase titanium dioxide has the ability to reflect and scatter light, which helps in achieving a vibrant and long-lasting color finish.
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2025-08-14 19:07
88
lithopone supplier 30% has a lower coverage power than titanium dioxide. For this reason, lithopone supplier 30% can only partially substitute titanium dioxide, between 5 and 40%.
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2025-08-14 18:57
1519
The first commercial production of TiO2 began in the early 20th century, using the sulfate process. This method involved reacting ilmenite ore with sulfuric acid to produce titanium sulfate, which was then calcined to obtain titanium dioxide. However, this process had several drawbacks, including high energy consumption, generation of large amounts of waste, and release of harmful gases such as sulfur dioxide. As a result, many factories transitioned to the chloride process, which offers higher purity TiO2 and reduced environmental impact.
trans-5-Octenal
Different dermal cell types have been reported to differ in their sensitivity to nano-sized TiO2 . Kiss et al. exposed human keratinocytes (HaCaT), human dermal fibroblast cells, sebaceous gland cells (SZ95) and primary human melanocytes to 9 nm-sized TiO2 particles at concentrations from 0.15 to 15 μg/cm2 for up to 4 days. The particles were detected in the cytoplasm and perinuclear region in fibroblasts and melanocytes, but not in kerati-nocytes or sebaceous cells. The uptake was associated with an increase in the intracellular Ca2+ concentration. A dose- and time-dependent decrease in cell proliferation was evident in all cell types, whereas in fibroblasts an increase in cell death via apoptosis has also been observed. Anatase TiO2 in 20–100 nm-sized form has been shown to be cytotoxic in mouse L929 fibroblasts. The decrease in cell viability was associated with an increase in the production of ROS and the depletion of glutathione. The particles were internalized and detected within lysosomes. In human keratinocytes exposed for 24 h to non-illuminated, 7 nm-sized anatase TiO2, a cluster analysis of the gene expression revealed that genes involved in the “inflammatory response” and “cell adhesion”, but not those involved in “oxidative stress” and “apoptosis”, were up-regulated. The results suggest that non-illuminated TiO2 particles have no significant impact on ROS-associated oxidative damage, but affect the cell-matrix adhesion in keratinocytes in extracellular matrix remodelling. In human keratinocytes, Kocbek et al. investigated the adverse effects of 25 nm-sized anatase TiO2 (5 and 10 μg/ml) after 3 months of exposure and found no changes in the cell growth and morphology, mitochondrial function and cell cycle distribution. The only change was a larger number of nanotubular intracellular connections in TiO2-exposed cells compared to non-exposed cells. Although the authors proposed that this change may indicate a cellular transformation, the significance of this finding is not clear. On the other hand, Dunford et al. studied the genotoxicity of UV-irradiated TiO2 extracted from sunscreen lotions, and reported severe damage to plasmid and nuclear DNA in human fibroblasts. Manitol (antioxidant) prevented DNA damage, implying that the genotoxicity was mediated by ROS.
Well asides from making you re-think that M & M addiction (chocolate coated in Titanium Dioxide…..anyone?!)
