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46140-16-3

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46140-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46140-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,1,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 46140-16:
(7*4)+(6*6)+(5*1)+(4*4)+(3*0)+(2*1)+(1*6)=93
93 % 10 = 3
So 46140-16-3 is a valid CAS Registry Number.

46140-16-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name bismuth(III) nitrate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:46140-16-3 SDS

46140-16-3Relevant articles and documents

A facile route to the synthesis of BiFeO3 at low temperature

Liu, Ting,Xu, Yebin,Feng, Shangshen,Zhao, Jingyuan

, p. 3060 - 3063 (2011)

A facile sol-gel methodology based on the glycerol-gel reaction was used to prepare single-phase BiFeO3 crystallites. The particle size and morphologies of BiFeO3 crystallites were characterized by field-emission scanning electron mi

Standard molar enthalpy of formation of [(C12H8N2)2Bi(O2NO)3] and its biological activity on Schizosaccharomyces pombe

Li, Chuan-Hua,Jiang, Yong,Jiang, Jian-Hong,Li, Xu,Xiao, Sheng-Xiong,Tao, Li-Ming,Yao, Fei-Hong,Zhang, Hui,Xia, Xian-Ming,Yao, Long-Hua,Zhou, Hua,Xiang, Ying-Hui,Tian, Yuan,Li, Qiang-Guo

, p. 1743 - 1751 (2017)

The title complex [(C12H8N2)2Bi(O2NO)3] was synthesized by reaction of 1,10-phenanthroline (phen) and Bi(NO3)3·5H2O. The structure of the complex was charac

Energy transfer study in GdVO4: Bi3+, Yb3+ obtained by microwave-assisted hydrothermal method

Lenczewska, Katarzyna,Ptak, Maciej,Boiko, Vitalii,Ledwa, Karolina,Hreniak, Dariusz

, (2021)

Influence of dopants on the structure, morphology and luminescence properties, and in particular the energy transfer mechanism of GdVO4 co-doped with Bi3+ and Yb3+ ions is discussed. Submicro- and microcrystals were prepared by the microwave-assisted hydrothermal method. Phase purity, size and structure of obtained samples were characterized by the X-ray powder diffraction and the transmission electron microscopy. Luminescence properties were investigated by analyzing photoluminescence and excitation spectra and decay time curves. Intense yellow-green luminescence from Bi3+ ions in the range of 400–800 nm and the near-infrared emission from Yb3+ ions about 1000 nm upon an indirect excitation via the (O2?–V5+) charge transfer state at 266 nm and via the (Bi3+–V5+) charge transfer state at 330 nm was recorded. No concentration quenching effect was observed in the samples doped with up to 7 mol% of Yb3+ ions. The near-ultraviolet sensitized near-infrared emission has been explained by the energy transfer from the GdVO4 host and Bi3+ ions to Yb3+ ions. The energy transfer processes between the host and dopants ions have been characterized in detail. The impact of phonon-assisted processes on the near infrared Yb3+ emission has been investigated. The obtained spectroscopic characteristics prove that GdVO4 co-doped with Bi3+ and Yb3+ ions is a promising candidate for use as the phosphor in luminescent concentrators in photovoltaic applications, which can increase the efficiency of silicon-based solar cells.

Dual-center thermochromic Bi2MoO6:Yb3+, Er3+, Tm3+ phosphors for ultrasensitive luminescence thermometry

Zheng, Teng,Runowski, Marcin,Stopikowska, Natalia,Skwierczyńska, Ma?gorzata,Lis, Stefan,Du, Peng,Luo, Laihui

, (2021/09/10)

Optical thermometers are of great interest due to their non-contact, high-sensitivity and fast measurement characteristics. In this work, a series of dual-center Bi1.96?xMoO6: 0.02Er3+, 0.02Tm3+, xYb3+ (x = 0.10–0.35) upconverting materials were prepared by a sol-gel synthesis method. Upon 975 nm excitation, the prepared materials exhibit bright color-tunable (from yellow to orange) upconversion (UC) emissions, as the Yb3+ content increases. The thermometric properties of the synthesized materials associated with different thermally-coupled and non-thermally coupled levels of Tm3+ and Er3+ were systematically investigated. Based on the temperature-dependent emissions originating from the non-thermally coupled levels of Tm3+ (3F2,3) and Er3+ (4F9/2), i.e., their band intensity ratios 700/670 nm, the developed optical thermometers were found to exhibit an exceptional relative thermal sensitivity (Sr), up to 5.90% K?1 at 293 K. Importantly, in the whole T-range of 293–623 K, the Sr values are larger than 2% K?1. Furthermore, it is revealed that the position of the Tm3+ emission band, centered around 800 nm is highly dependent on temperature, and, so, it can be utilized as a second thermometric parameter, which is important for a multi-parameter temperature sensing in the T-range of 293–623 K. These results suggest that Er3+/Tm3+/Yb3+-doped Bi2MoO6 materials are promising candidates for ultra-sensitive, dual mode optical thermometers and safety sign applications.

Preparation method of bismuth subgallate

-

Paragraph 0031, (2017/05/27)

The invention provides a preparation method of bismuth subgallate, comprising the following steps: Step (1), adding bismuth trioxide into concentrated nitric acid to dissolve bismuth trioxide, and then adding deionized water to obtain a bismuth nitrate solution; Step (2) adding deionized water into gallic acid to dissolve gallic acid so as to obtain a gallic acid aqueous solution; Step (3), adding the gallic acid aqueous solution into the bismuth nitrate solution at the molar ratio of gallic acid in the gallic acid aqueous solution to bismuth nitrate in the bismuth nitrate solution being 1.1:1-1.2:1, so as to obtain a yellow precipitate; and Step (4) filtering the yellow precipitate to obtain a filter cake, washing the filter cake with deionized water and finally drying so as to obtain bismuth subgallate. The preparation method of bismuth subgallate is simple to operate and is cost-saving.

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