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International Dioxcides patent pending design integrates the highest levels of safety, functionality, and industrial robustness in a self-contained modular design that is easy to install. Uses: Chlorinedioxide generation systems. Group: Chlorinedioxide systems. Categories: ChlorineDioxide Generators.
International Dioxcide
ADOX MG II Generator
The ADOX MG II uses chlorine gas to react with the precursor sodium chlorite to generate chlorinedioxide and is certified by NSF for standard 61. Uses: Chlorinedioxide generation systems. Group: Chlorinedioxide systems. Categories: ChlorineDioxide Generators.
International Dioxcide
ADOX MG III Generator
The ADOX MG III uses sodium hypochlorite (bleach) and hydrochloric acid to react with the precursor sodium chlorite to generate chlorinedioxide and is certified by NSF under standard 61. Uses: Chlorinedioxide generation systems. Group: Chlorinedioxide systems. Categories: ChlorineDioxide Generators.
International Dioxcide
ADOX Mini-AC Generator
The highly popular acid/chlorite reaction chemistry utilized in the MiniAC generator efficiently generates 7 lbs. to 30 lbs. of chlorinedioxide daily without the need for any electrical hookups. Uses: Chlorinedioxide generation systems. Group: Chlorinedioxide systems. Categories: ChlorineDioxide Generators.
International Dioxcide
PurDOX Generator ,"λ","λ"
The PurDOX 700 VB is a complete chlorinedioxide generator in a self-contained modular design that is easy to install and requires a small footprint. Uses: Chlorinedioxide generation systems. Group: Chlorinedioxide systems. Categories: ChlorineDioxide Generators.
International Dioxcide
Ruthenium dioxide
Ruthenium dioxide is one of the primary oxygen catalysts used in a majority of chemical reactions such as the production of chlorine oxides. Ruthenium (IV) oxide is applied as an electrochemical supercapacitor agent as it has a high potential to store charge. Ruthenium dioxide is applied as a catalyst in the Deacon process where chlorine is produced through oxidation of hydrogen chloride. The high charge potential makes Ruthenium dioxide appropriate for use as an active agent in supercapacitors. The dispersion aspect of Ruthenium dioxide enhances the capacitance of nanocomposite electrode substances for supercapacitors. Ruthenium dioxide is widely used as a doping agent, as a catalyst, and as a coating material for titanium anodes, for the elimination of hydrogen sulfide from oil refineries. Hydrogen sulfide can be divided by light in the presence of a photocatalyst-containing CdS crystals doped with Ruthenium (IV) oxide. The hydrogen obtained could be essential in the synthesis of methanol, ammonia and potentially fuel an economy driven by hydrogen. Group: Nanoparticles & nanopowders. Alternative Names: Dioxoruthenium. CAS No. 12036-10-1. Molecular formula: O2Ru. Mole weight: 133.1. Appearance: Dark blue crystal. Purity: 0.98. IUPACName: dioxoruthenium. Canonical SMILES: O=[Ru]=O. ECNumber: 234-840-6. Catalog: ACM12036101-4.
Ruthenium dioxide
Ruthenium dioxide. Uses: Ruthenium dioxide is one of the primary oxygen catalysts used in a majority of chemical reactions such as the production of chlorine oxides. ruthenium (iv) oxide is applied as an electrochemical supercapacitor agent as it has a high potential to store charge. ruthenium dioxide is applied as a catalyst in the deacon process where chlorine is produced through oxidation of hydrogen chloride. the high charge potential makes ruthenium dioxide appropriate for use as an active agent in supercapacitors. the dispersion aspect of ruthenium dioxide enhances the capacitance of nanocomposite electrode substances for supercapacitors. ruthenium dioxide is widely used as a doping agent, as a catalyst, and as a coating material for titanium anodes, for the elimination of hydrogen sulfide from oil refineries. hydrogen sulfide can be divided by light in the presence of a photocatalyst-containing cds crystals doped with ruthenium (iv) oxide. the hydrogen obtained could be essential in the synthesis of methanol, ammonia and potentially fuel an economy driven by hydrogen. Group: Salt. Alternative Names: Dioxoruthenium. CAS No. 12036-10-1. Product ID: dioxoruthenium. Molecular formula: 133.1. Mole weight: O2Ru. O=[Ru]=O. InChI=1S/2O.Ru. WOCIAKWEIIZHES-UHFFFAOYSA-N. 98%.
Sodium Chlorate
International Dioxcide manufactures a proprietary mixture of sodium chlorate and hydrogen peroxide, which is used to produce chlorinedioxide for biocidal and oxidative water treatment applications. Uses: Chemical precursors. Group: sodium chlorate. Categories: NaClO3.
International Dioxcide
Sodium Chlorate
Sodium Chlorate is used in the preparation of chlorinedioxide solution use in water treatment, as a food preservative agent, an antiseptic and also as a deodorant. Group: Biochemicals. Grades: Highly Purified. CAS No. 7775-9-9. Pack Sizes: 5g, 25g. Molecular Formula: ClNaO3. US Biological Life Sciences.
Worldwide
1,4-Dioxane
1,4-Dioxane is a heterocyclic organic compound that is commonly used as a solvent in several chemical reactions. It is also used as a stabilizer in chlorinated solvents. Uses: 1,4-dioxane is used as a stabilizer for 1,1,1-trichloroethane and chlorinated solvents. it acts as a solvent for cellulose acetate, ethyl cellulose, benzyl cellulose, resins, oils, waxes, dyes, other organic and inorganic compounds. it acts as a substitute for tetrahydrofuran due to its higher boiling point and lower toxicity. further, it is used as an internal standard for proton nmr spectroscopy in deuterium oxide. it plays an important role in liquid scintillation counting in biological procedures, and as a wetting and dispersing agent in textile processing. it is involved in the preparation of dimethylmagnesium by reacting with methylmagnesium bromide, and in the preparation of histological sections for microscopic examination. Group: Solvents. Alternative Names: dioxane dioxane, technical grade dioxaan-1,4 dioxane-1,4 glycol ethylene ether 1,4-dioxanne glycolethylenether diethylene dioxide dioxan-1,4 diossano-1,4. CAS No. 123-91-1. Molecular formula: C4H8O2. Mole weight: 88.11. IUPACName: 1,4-dioxane. Canonical SMILES: C1COCCO1. Density: 1.033 g/mL. ECNumber: 204-661-8. Catalog: ACM123911-1.
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