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Eg c2h6o2

Manufactured by Merck Group
Sourced in United States

EG (C2H6O2) is a colorless, odorless liquid used in various industrial and laboratory applications. It is a common component in laboratory equipment and serves as a key ingredient in many chemical processes.

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2 protocols using eg c2h6o2

1

Spongy Ni, Co and Ni-Co Alloy Synthesis

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36 g of Ni(NO3)2.6H2O (Sigma-Aldrich) was added to 18 mL of EG (C2H6O2) (Sigma-Aldrich) and ultra-sonicated for 1 hour. After that the resultant mixture was poured into a cylindrical crystalline glass dish, which was pre-heated to a temperature of 300 °C for 30 minutes by using a hot plate in the ambient atmosphere. A sudden introduction of reactants in to the hot glass dish leads to the evolution of NO2 gas bubbles and subsequent production of fluffy Ni sponge. Cobalt oxide (Co3O4) sponge was prepared by the reaction of Co(NO3)2.6H2O (36 g) and EG (18 mL) by using the same procedure mentioned above for Ni sponge. The same synthesis route is followed for the preparation of Ni-Co alloy sponges. Here reactants Ni(NO3)2.6H2O and Co(NO3)2.6H2O (sigma-Aldrich), were mixed together taking a total amount of 36 g in the weight ratio of 1:1, 1:2 and 2:1 and the resulting sponges named as Ni1Co1, Ni1Co2 and Ni2Co1. For the synthesis of Ni-NG, 36 g of Ni(NO3)2.6H2O (Sigma-Aldrich) and 100 mg of NG(prepared by heating GO with melamine (1:5 ratio) for 3 hrs at 800 °C)51 (link) were added to 18 mL of EG (C2H6O2) (Sigma-Aldrich) and ultra-sonicated for 1 hour. The resultant mixture was poured in to a cylindrical dish preheated for 1 hour leads to the formation of Ni-NG sponges.
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2

Synthesis of Vertically Oriented Titanium Nanotubes

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Highly ordered and vertically oriented TNTs were prepared by anodization of Ti (titanium foil, 0.25-mm thickness, 99.7% purity; Sigma-Aldrich, St. Louis, MO, USA) sheets in an electrolyte consisting of 0.25 wt.% ammonium fluoride (NH4F) (98 + % purity; Sigma-Aldrich) and 0.5 wt.% distilled (DI) water in ethylene glycol (EG) (C2H6O2, 99.0% purity; Sigma-Aldrich) at 40 V for 8 h. A detailed experimental procedure has been described in our previous paper
[25 (link)]. After anodization, the samples were washed with DI water to remove the occluded ions and dried in a N2 stream. Finally, the samples were annealed at 450°C for 2 h with a heating rate of 5°C min-1 at ambient conditions.
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