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产品线
AnhydroBeads™
质量水平
方案
99.99% trace metals basis
杂质
≤150.0 ppm Trace Metal Analysis
粒径
−10 mesh
mp
677 °C (lit.)
密度
3.16 g/mL at 25 °C (lit.)
应用
battery manufacturing
SMILES字符串
Cl[Fe]Cl
InChI
1S/2ClH.Fe/h2*1H;/q;;+2/p-2
InChI key
NMCUIPGRVMDVDB-UHFFFAOYSA-L
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一般描述
氯化亚铁,别名二氯化铁,是高熔点的顺磁固体。因其独特性质广泛应用于太阳能电池、燃料电池催化剂和半导体中。也用作氧化还原反应的还原剂,在电化学过程中发挥重要作用。
应用
氯化亚铁用处:
- 作为制造有机-无机混合钙钛矿的掺杂剂用于制备高效的钙钛矿太阳能电池。氯化亚铁可提高太阳能电池的总体效率。
- 作为前体合成各种二价铁配位化合物。这些配合物由于独特的光学电学特性,在太阳能转换和催化等诸多应用中发挥重要作用。
- 作为前体合成铁-氮-碳(Fe–N–C)催化剂用于制备质子交换膜染料电池。
法律信息
AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC
警示用语:
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Eye Dam. 1
储存分类代码
8B - Non-combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
does not flash
闪点(°C)
does not flash
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
历史批次信息供参考:
分析证书(COA)
Inorganic Chemistry, 37, 612-612 (1998)
Water research, 46(16), 5255-5267 (2012-07-25)
Various iron oxy-hydroxides were synthesized in a continuous flow kilogram-scale production reactor through the precipitation of FeSO(4) and FeCl(2) in the pH range 3-12 under intense oxidative conditions to serve as arsenic adsorbents. The selection of the optimum adsorbent and
The Journal of organic chemistry, 77(20), 9366-9373 (2012-10-03)
Iron-catalyzed direct C-N bond formation between azoles and amides is described. The oxidative coupling reactions of sp(3) C-H bonds adjacent to a nitrogen atom in amides and sulfonamides with the N-H bond in azoles proceeded smoothly in the presence of
Journal of food science, 77(1), C8-14 (2011-12-21)
Wines made from 3 spine grape (Vitis davidii Foex) genotypes-Junzi 1# (JZ 1#), Junzi 2# (JZ 2#), and Liantang (LT)-and Cherokee rose (Rosa laevigata Michx., CR) were evaluated for their phenolics composition and antioxidant activities by several assays, including 2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulfonic
Angewandte Chemie (International ed. in English), 51(28), 6971-6975 (2012-06-13)
Ironing it out: an efficient and convenient nitrogenation strategy involving C-C bond cleavage for the straightforward synthesis of versatile arylamines is presented. Various alkyl azides and alkylarenes, including the common industrial by-product cumene, react using this protocol. Moreover, this method
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