BISMUTH GALLATE
BISMUTH SUBGALLATE
CAS: 99-26-3
Molecular Formula: C7H5BiO6
BISMUTH GALLATE - Names and Identifiers
| Name | BISMUTH SUBGALLATE |
| Synonyms | DERMATOL Dermatol Puder BISMUTH GALLATE Bismuthsubgarate Bismuthoxygallate BISMUTH SUBGALLATE |
| CAS | 99-26-3 |
BISMUTH GALLATE - Physico-chemical Properties
| Molecular Formula | C7H5BiO6 |
| Molar Mass | 394.10(anhy) |
| Melting Point | 223 °C (dec.)(lit.) |
| Storage Condition | Room Temprature |
| MDL | MFCD01632692 |
| Physical and Chemical Properties | Bright yellow crystal, odorless, tasteless. Almost insoluble in water, alcohol, ether and chloroform, and soluble in dilute alkali. |
| Use | Use of the product for the convergence of drugs and antiseptic, external for eczema and other skin diseases. |
BISMUTH GALLATE - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| UN IDs | 20/21/22 |
BISMUTH GALLATE - Preparation Method of basic bismuth gallate
from Baidu Library
Application (patent) number:
CN201310321103.3
Public/Announcement Number:
CN103342722 A
applicant (patent):
Taishan Xinning Pharmaceutical Co., Ltd.
inventor:
cited:
Abstract:
A method for preparing basic bismuth gallate from gallic acid and industrial bismuth nitrate using a modified polyacrylamide-co-styrene-co-acrylic acid copolymer as an adsorption material, removal of heavy metals from industrial bismuth nitrate raw materials by adsorption; the modified copolymer is prepared by modifying a polyacrylamide-co-styrene-co-acrylic acid copolymer raw material with formaldehyde and dimethylamine and optionally a C2-C4 organic amine containing a mercapto group, hydroxymethyl (-CH2-OH) and aminomethyl (-CH2-N(CH3)2) were introduced into the side chain of the copolymer, and optionally with or without the introduction of mercapto (-SH) or Thio (-S-) groups on the side chains of the copolymer. The modified copolymer has an outstanding ability to adsorb heavy metals such as lead, cadmium, mercury and arsenic.
Last Update：2024-01-02 23:10:35
BISMUTH GALLATE - Preparation, characterization and combustion catalysis of bismuth-zirconium gallate
from VIP Journal Professional Edition
Author:
Zhao Fengqi , Zhang Heng , Anting , Zhang Xiaohong , yijianhua , Xu Siyu , Wang Yinglei
Abstract:
with gallic acid , bismuth nitrate and zirconium nitrate as raw materials, a bimetallic organic salt-bismuth-zirconium gallate was synthesized for the first time, it was characterized by organic elemental analysis, X-ray fluorescence (XRF) spectroscopy and Fourier transform infrared (FTIR) spectroscopy. Under the condition of temperature programming, thermogravimetry (TG) analysis, differential scanning calorimetry (DSC), solid phase in situ reaction cell/FTIR, the thermal behavior and thermal decomposition mechanism of bismuth zirconium gallate were studied. The thermal decomposition process of bismuth zirconium gallate was described, and the final decomposition products were Bi2O3,ZrO2 and C. The propellant samples containing bismuth-zirconium gallate were prepared by spiral pressing process. The effect of bismuth-zirconium gallate on the combustion performance of double base (DB) propellant was studied, and its combustion catalysis was analyzed. The results show that bismuth-zirconium gallate has a good catalytic effect on the combustion of double-base propellant, and it is an efficient combustion catalyst. The final product of thermal decomposition of bismuth-zirconium gallate is the main material of catalytic combustion, zirconium and carbon play the role of auxiliary catalysis.
expand
Key words:
physical chemistry bismuth zirconium gallate propellant thermal behavior decomposition mechanism combustion performance catalytic action
DOI:
CNKI:SUN:WLHX.0.2013-04-019
year:
2013
Last Update：2024-01-02 23:10:35
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View History
BISMUTH GALLATE
卡维丁
溶剂棕
methyl threoninate
MK 0677
978-76-7
Nitrobenzene-d5
青霉素钾
cyclohexanecarboxylic acid, 4-oxo-, methyl ester
5-Fluoro-2-nitrophen
卡维丁
溶剂棕
methyl threoninate
MK 0677
978-76-7
Nitrobenzene-d5
青霉素钾
cyclohexanecarboxylic acid, 4-oxo-, methyl ester
5-Fluoro-2-nitrophen