The analytical reagents employed in this study were tin (II) chloride (SnCl2·2H2O, Sigma-Aldrich), thioacetamide (C2H5NS, Sigma-Aldrich, St. Louis, MO, USA), ethylenediaminetetraacetic acid (EDTA, C10H16N2O8, Sigma-Aldrich, St. Louis, USA), and acetone (C3H6O, Sigma-Aldrich, St. Louis, USA), used as received without further purification and stored in a humidity-controlled desiccator cabinet. For the preparation of π-SnS nanoparticles, SnCl2·2H2O and C2H5NS were used as Sn and S sources, respectively, and C10H16N2O8 was used as a chelating agent.
C10h16n2o8
Manufactured by Merck Group
Sourced in United States
C10H16N2O8 is a chemical compound commonly used as a reagent in various laboratory applications. It serves as a core component for a range of analytical and research procedures. The detailed function and intended use of this product should be addressed by our technical team.
Automatically generated - may contain errors
Lab products found in correlation
Sncl2 2h2o, by Merck Group (1 mentions)
C3h6o, by Merck Group (1 mentions)
C2h5ns, by Merck Group (1 mentions)
Benzoquinone c6h4o2, by Merck Group (1 mentions)
Sodium dodecyl sulfate (sds), by Merck Group (1 mentions)
Potassium hydroxide, by Merck Group (1 mentions)
Ethylene diamine tetraacetic acid (edta), by Merck Group (1 mentions)
Sodium borohydride, by Merck Group (1 mentions)
Copper sulfate, by Merck Group (1 mentions)
Anhydrous citric acid, by Merck Group (1 mentions)
Nh4oh, by Merck Group (1 mentions)
Ce no3 3 6h2o, by Merck Group (1 mentions)
Nd no3 3 6h2o, by Merck Group (1 mentions)
4 protocols using c10h16n2o8
1
Synthesis of π-SnS Nanoparticles
2
Titanium-based Photocatalyst Synthesis
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All chemicals were of analytical grade and used without further purification: titanium (IV) i-propoxide (TTIP, Merck, Kenilworth, NJ, USA, 98%), hydrochloric acid (HCl, Chemsolute, Th. Geyer, Berlin, Germany, 35–38%), cinnamic acid (C9H8O2, Reachim, Moscow, Russia, 99%), ibuprofen sodium salt (C13H17O2Na, Sigma-Aldrich, St. Louis, MA, USA, 98%), ethylenediaminetetraacetic acid (C10H16N2O8, Sigma-Aldrich, 99%), i-propanol (C3H8O, Sigma-Aldrich, >99%), tert-butanol (C4H10O, Sigma-Aldrich, 99%), benzoquinone (C6H4O2, Sigma-Aldrich, ≥98%), and titania P25 (TiO2, Evonik, Essen, Germany, 99.5%).
3
Synthesis of Copper Nanoparticles
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Copper sulfate, CuSO4 (≥98%); sodium borohydride, NaBH4 (98%);
ethylenediaminetetraacetic acid, EDTA, C10H16N2O8 (≥98%); potassium hydroxide, KOH
(90%); sodium dodecyl sulfate, SDS (≥99%); and poly(vinylpyrrolidone),
PVP-300 K (99%) were purchased from Sigma-Aldrich Peru (Lima, Peru).
All chemicals were of analytical purity and used as received without
further purification. Milli-Q water (18 MΩ cm) was used in all
experimental syntheses. The purification system (Millipore, Darmstadt,
Germany) is located in our laboratory.
ethylenediaminetetraacetic acid, EDTA, C10H16N2O8 (≥98%); potassium hydroxide, KOH
(90%); sodium dodecyl sulfate, SDS (≥99%); and poly(vinylpyrrolidone),
PVP-300 K (99%) were purchased from Sigma-Aldrich Peru (Lima, Peru).
All chemicals were of analytical purity and used as received without
further purification. Milli-Q water (18 MΩ cm) was used in all
experimental syntheses. The purification system (Millipore, Darmstadt,
Germany) is located in our laboratory.
4
Synthesis of Cerium-Neodymium Oxide Nanocomposites
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Ce1−xNdxO2−δ (x = 0, 0.05, 0.1 and 0.2) were synthesized by the combined EDTA–citrate complexing method.22 (link) Firstly, stoichiometric amounts of the corresponding metal nitrates (Ce(NO3)3·6H2O, 99.0% Sigma-Aldrich and Nd(NO3)3·6H2O, 99.9% Sigma-Aldrich) were dissolved in deionized water. The solution was heated to 70 °C and stirred during 1 h. Anhydrous citric acid (C6H8O7 99.98%, Sigma-Aldrich) and EDTA (C10H16N2O8 98.5%, Sigma-Aldrich) were separately dissolved in an ammonium hydroxide dissolution (NH4OH 28–30%, Sigma-Aldrich), controlling the pH value at around 7. Then, these two solutions were heated to 90 °C under stirring and subsequently dropped simultaneously to the aqueous metal nitrates-containing solution. The pH of the resultant solution was monitored and keep at around 7 by dropping an excess of aqueous ammonia solution. The molar ratio was 1 : 1 : 1 for metal cations : citric acid : EDTA. A transparent solution was obtained and subsequently heated to 90 °C, while it was stirred. After water evaporation, a viscous gel was obtained. Then the gel was combusted at about 300 °C to remove the organic matter. The resultant yellow powder was calcined at 500 °C for 8 h under air atmosphere.
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