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The main use of copper(I) chloride is as a precursor to the fungicide copper oxychloride. For this purpose aqueous copper(I) chloride is generated by comproportionation and then air-oxidized: [12] Cu + CuCl 2 → 2 CuCl 4 CuCl + O 2 + 2 H 2 O → Cu 3 Cl 2 (OH) 4 + CuCl 2. Copper(I) chloride catalyzes a variety of organic reactions, as
Copper(II) chloride is used as a catalyst in a variety of processes that produce chlorine by oxychlorination. The Deacon process takes place at about 400 to 450 °C in the presence of a copper chloride: [8] 4 HCl + O 2 → 2 Cl 2 + 2 H 2 O. Copper(II) chloride catalyzes the chlorination in the production of vinyl chloride and dichloromethane. [8]
The use of copper pesticide in viticulture in 1940. Copper pesticide is applied as a contact protective foliar spray, so it remains deposited on leaf surfaces. A small concentration of copper ions may be taken up by plants as essential nutrients. Copper foliar sprays are also applied to correct plant copper deficiency. [8]
Recognition that basic copper chloride would reduce feed stability problems led to issuance of patents on the use of the compound as a nutritional source. Subsequently, animal feeding studies revealed that the alpha crystal form of basic copper chloride has a rate of chemical reactivity that is well matched to biological processes.
This is a list of fungicides.These are chemical compounds which have been registered as agricultural fungicides.The names on the list are the ISO common name for the active ingredient which is formulated into the branded product sold to end-users. [1]
Copper alloy surfaces have intrinsic properties that destroy many microorganisms.In the interest of protecting public health, especially in healthcare environments with their susceptible patient populations, an abundance of peer-reviewed antimicrobial efficacy studies have been conducted in the past ten years regarding copper's efficacy to destroy E. coli O157:H7, methicillin-resistant ...
This results in a combination of copper oxide and pure copper nanoparticle clusters, depending on the method used. A more modern synthesis utilizes copper(II) chloride in a room temperature reaction with sodium citrate or myristic acid in an aqueous solution containing sodium formaldehyde sulfoxylate to obtain a pure copper nanoparticle powder. [5]
Work by Hosokawa and coworkers [21] yielded a crystallized product containing copper chloride, indicating it may have a non-innocent role in olefin oxidation. Finally, an ab initio study by Comas-Vives, et al. [22] involving no copper co-catalyst found anti-addition was the preferred pathway. This pathway was later confirmed by copper-free ...