Cupric chloride dihydrate (CuCl2·2H2O, 99%), tetrachloroaurate trihydrate (HAuCl4·3H2O, 99%) and glucose (α or β form) were purchased from Sinopharm Chemical Reagent Co. Ltd (Shanghai, China). HDA (90%) was obtained from Sigma-Aldrich. All the vials were made from borosilicate glass, with a black phenolic-moulded screw cap and polyvinyl-faced pulp liner. Ultrapure Millipore water (18.2 MΩ) was used as the solvent throughout.
Cupric chloride dihydrate
Manufactured by Sinopharm
Sourced in China
Cupric chloride dihydrate is an inorganic compound with the chemical formula CuCl2·2H2O. It is a crystalline solid that appears green in color. The compound serves as a source of copper(II) ions and is commonly used in various laboratory applications.
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Lab products found in correlation
2 protocols using cupric chloride dihydrate
1
Synthesis of Au-Cu Nanoalloy Catalysts
2
Synthesis of CCNTs and N-GQDs
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CV was purchased from Shanghai Yuanye Bio-Technology Co., Ltd., cupric chloride dihydrate, citric acid monohydrate, and potassium persulfate were obtained from Sinopharm Chemical Reagent Co., Ltd., China. Phosphate-buffered saline (PBS) solutions with various pH values were prepared by stock solution of 0.1 mol/L KH2PO4 and K2HPO4. All other chemicals were of analytical grade and used without further purification. The solutions were prepared by using doubly distilled water.
The CCNTs were prepared as follows: 0.2 g CNTs were added into 100 mL 3:1 (v/v) H2SO4:HNO3, then refluxed at 120°C for 1 h, the solution was finally filtered using a 0.8-μm membrane. The residue was washed by water until pH = 7 and dried in an oven at 60°C for 8 h to obtain the CCNTs.
The N-GQDs were prepared as followes: 8.0 g citric acid monohydrate and 1.0 mL ammonia were added into an autoclave and heated at 210°C for 1.5 h, and then cooled to room temperature naturally. After cooling to room temperature, the N-GQDs solution was mixed with excess ethanol, allowed to stay there for 15 min, and then centrifuged at 13000 rpm for 5 min to remove any impurities. After purification, the resultant N-GQDs was diluted to 50 mL with water for further use.
The CCNTs were prepared as follows: 0.2 g CNTs were added into 100 mL 3:1 (v/v) H2SO4:HNO3, then refluxed at 120°C for 1 h, the solution was finally filtered using a 0.8-μm membrane. The residue was washed by water until pH = 7 and dried in an oven at 60°C for 8 h to obtain the CCNTs.
The N-GQDs were prepared as followes: 8.0 g citric acid monohydrate and 1.0 mL ammonia were added into an autoclave and heated at 210°C for 1.5 h, and then cooled to room temperature naturally. After cooling to room temperature, the N-GQDs solution was mixed with excess ethanol, allowed to stay there for 15 min, and then centrifuged at 13000 rpm for 5 min to remove any impurities. After purification, the resultant N-GQDs was diluted to 50 mL with water for further use.
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