349151
Kupfer
foil, thickness 0.5 mm, 99.98% trace metals basis
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About This Item
Empirische Formel (Hill-System):
Cu
CAS-Nummer:
Molekulargewicht:
63.55
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
11101604
PubChem Substanz-ID:
NACRES:
NA.23
Empfohlene Produkte
Qualitätsniveau
Assay
99.98% trace metals basis
Form
foil
Widerstandsfähigkeit
1.673 μΩ-cm, 20°C
Dicke
0.5 mm
bp
2567 °C (lit.)
mp (Schmelzpunkt)
1083.4 °C (lit.)
Dichte
8.94 g/mL at 25 °C (lit.)
Anwendung(en)
battery manufacturing
SMILES String
[Cu]
InChI
1S/Cu
InChIKey
RYGMFSIKBFXOCR-UHFFFAOYSA-N
Allgemeine Beschreibung
Copper is a versatile metal crucial in catalysis and material science. Its excellent electrical and thermal conductivity, ductility, and corrosion resistance make it ideal for conductive materials. Additionally, copper serves as a catalyst in various chemical reactions, facilitating electron transfer and promoting redox processes, including reduction, cross-coupling, and "click" chemistry, such as copper-catalyzed azide-alkyne cycloaddition reactions.
Anwendung
- LaCl(3)-based sodium halide solid electrolytes with high ionic conductivity for all-solid-state batteries.: This article presents the development of LaCl3-based sodium halide solid electrolytes, with a focus on improving ionic conductivity using copper additives, aiming to advance the efficiency and safety of all-solid-state batteries (Fu et al., 2024).
- Three-in-One Zinc Anodes Created by a Large-scale Two-Step Method Achieving Excellent Long-Term Cyclic Reversibility and Thin Electrode Integrity.: This research introduces a novel two-step method for creating zinc anodes, incorporating copper to achieve superior cyclic reversibility and electrode integrity, thus enhancing the longevity and performance of batteries (Lu et al., 2024).
- Scanning Electrochemical Microscopy Meets Optical Microscopy: Probing the Local Paths of Charge Transfer Operando in Booster-Microparticles for Flow Batteries.: This study combines scanning electrochemical and optical microscopy to analyze the local charge transfer paths in booster-microparticles, using copper as a key component for improving the operando analysis in flow batteries (Moghaddam et al., 2024).
Menge
11 g = 50 × 50 mm; 99 g = 150 × 150 mm
Lagerklassenschlüssel
13 - Non Combustible Solids
WGK
WGK 2
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Hiroshi Sato et al.
Science (New York, N.Y.), 343(6167), 167-170 (2013-12-18)
Carbon monoxide (CO) produced in many large-scale industrial oxidation processes is difficult to separate from nitrogen (N2), and afterward, CO is further oxidized to carbon dioxide. Here, we report a soft nanoporous crystalline material that selectively adsorbs CO with adaptable
Seonah Kim et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(1), 149-154 (2013-12-18)
Lytic polysaccharide monooxygenases (LPMOs) exhibit a mononuclear copper-containing active site and use dioxygen and a reducing agent to oxidatively cleave glycosidic linkages in polysaccharides. LPMOs represent a unique paradigm in carbohydrate turnover and exhibit synergy with hydrolytic enzymes in biomass
Stephen G Kaler et al.
The New England journal of medicine, 358(6), 605-614 (2008-02-08)
Menkes disease is a fatal neurodegenerative disorder of infancy caused by diverse mutations in a copper-transport gene, ATP7A. Early treatment with copper injections may prevent death and illness, but presymptomatic detection is hindered by the inadequate sensitivity and specificity of
Daniel L Priebbenow et al.
Organic letters, 15(24), 6155-6157 (2013-11-28)
A method has been developed for the preparation of N-alkynylated sulfoximines involving the copper-catalyzed decarboxylative coupling of sulfoximines with aryl propiolic acids. A range of substituents on both the sulfoximidoyl moiety and the aryl group of the propiolic acid were
Huawen Huang et al.
Organic letters, 15(24), 6254-6257 (2013-11-23)
A rapid and environmentally friendly conversion of pyridine to imidazo[1,2-a]pyridines has been developed via copper-catalyzed aerobic dehydrogenative cyclization with ketone oxime esters.
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