Deciphering an Abnormal Layered-Tunnel Heterostructure Induced by Chemical Substitution for the Sodium Oxide Cathode

Demands for large-scale energy storage systems have driven the development of layered transition-metal oxide cathodes for room-temperature rechargeable sodium ion batteries (SIBs). Now, an abnormal layered-tunnel heterostructure Na_0.44Co_0.1Mn_0.9O₂ cathode material induced by chemical element substitution is reported. By virtue of beneficial synergistic effects, this layered-tunnel electrode shows outstanding electrochemical performance in sodium half-cell system and excellent compatibility with hard carbon anode in sodium full-cell system. The underlying formation process, charge compensation mechanism, phase transition, and sodium-ion storage electrochemistry are clearly articulated and confirmed through combined analyses of in situ high-energy X-ray diffraction and ex situ X-ray absorption spectroscopy as well as operando X-ray diffraction. This crystal structure engineering regulation strategy offers a future outlook into advanced cathode materials for SIBs.     

Widely Adaptable Oil-in-Water Gel Emulsions Stabilized by an Amphiphilic Hydrogelator Derived from Dehydroabietic Acid

A surfactant, R-6-AO, derived from dehydroabietic acid has been synthesized. It behaves as a highly efficient low-molecular-weight hydrogelator with an extremely low critical gelation concentration (CGC) of 0.18 wt % (4 mm ). R-6-AO not only stabilizes oil-in-water (O/W) emulsions at concentrations above its critical micelle concentration (cmc) of 0.6 mm , but also forms gel emulsions at concentrations beyond the CGC with the oil volume fraction freely adjustable between 2 % and 95 %. Cryo-TEM images reveal that R-6-AO molecules self-assemble into left-handed helical fibers with cross-sectional diameters of about 10 nm in pure water, which can be turned to very stable hydrogels at concentrations above the CGC. The gel emulsions stabilized by R-6-AO can be prepared with different oils (n-dodecane, n-decane, n-octane, soybean oil, olive oil, tricaprylin) owing to the tricyclic diterpene hydrophobic structure in their molecules that enables them to adopt a unique arrangement in the fibers.     

Masking effect of potassium iodide on the interferences in the atomic-absorption spectrophotometric determination of antimony utilizing stibine generation by sodium borohydride tablet reduction

Summary The masking effect of potassium iodide with or without hydroxylamine on the interferences in the atomic-absorption spectrophotometric determination of antimony via its hydride by sodium borohydride tablet reduction has been studied. It has been well known in the conventional colorimetric method [21] that both potassium iodide and stannous chloride completely suppress the evolution of stibine. However, in this sodium borohydride tablet reduction, potassium iodide plays a role in masking the interferences of not only stannous chloride but also other numerous ions. By the procedure established here, the calibration curve was linear up to a concentration of 0.04g/ml of antimony with the coefficient of variation of 2.4 %. The method was successfully applied to the determination of antimony in a river sediment.

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Maskierende Wirkung von Kaliumiodid auf Störungen bei der AAS-Bestimmung von Antimon durch Stibinerzeugung mit Hilfe der Natriumborhydridreduktion

Zusammenfassung Es ist bekannt, daß bei der colorimetrischen Bestimmungsmethode [21] sowohl KI als auch SnCl₂ die Entwicklung von Stibin vollständig verhindern. Bei der hier beschriebenen Reduktion mit Hilfe einer NaBH₄-Tablette maskiert jedoch KI (mit oder ohne Hydroxylaminzusatz) Störungen durch SnCl₂ sowie durch zahlreiche andere Ionen. Die Eichkurve verläuft bis zu 0,04 g Sb/ml linear. Der Variationskoeffizient beträgt 2,4 %. Als Anwendungsbeispiel wird die Antimonbestimmung in Flußsedimenten erwähnt.

     

Untersuchung des Einflusses der Joddetektion bei aromatischen Verbindungen mit ?therisch gebundenem Sauerstoff im Ring, in der Alkoxygruppe, oder in der Phenolgruppe

Ohne Zusammenfassung

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Study of the influence of iodine detection on aromatic substances with oxygen in the ring, the alkoxy group or the phenol group