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Detail of "10361-44-1"

  • MSDS Download
  • CAS Number:
  • 10361-44-1
  • Name:
  • Nitric acid,bismuth(3+) salt (3:1)

  • Superlist Name:
  • Bismuth nitrate
  • Molecular Structure:
  • Formula:
  • Bi(NO3)3
  • Molecular Weight:
  • 394.99
  • Deleted CAS:
  • 35938-70-6,30880-06-9,20394-23-4,15008-64-7,14550-88-0,13536-44-2
  • Synonyms:
  • Bismuthnitrate (Bi(NO3)3) (6CI,7CI);Nitric acid, bismuth(3+) salt (8CI,9CI);Bismuthnitrate;Bismuth trinitrate;Bismuth(3+) nitrate;Bismuth(III) nitrate;
  • EINECS:
  • 233-791-8
  • Density:
  • 2.83 g/cm3
  • Melting Point:
  • 30 °C
  • Transport Information:
  • UN 1477

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CAS No.10361-44-1 Bismuth nitrate

Bismuth Nitrate MW: 485.07 MF: Bi(NO3)3 Grade: USP27 Description:Bismuth nitrate pentahydrate belongs to five-color triclinic system crystal, owns hydroscopicity and sour flavor. Its relative density is 2.83. Easily hydrolyze to produce basic bismuth nitrate. It is soluble

Supplier:Shenyang Delishun Chemical Co., Ltd. [ China (Mainland)]

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CAS No.10361-44-1 Bismuth nitrate

BISMUTH? NITRATE

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CAS No.10361-44-1 Bismuth nitrate

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CAS No.10361-44-1 Bismuth nitrate

BISMUTH NITRATE

Supplier:IS Chemicals Co., Ltd. [ Korea]

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CAS No.10361-44-1 Bismuth nitrate

Supplier:Yixing Xingping Chemical Co.,Ltd. (Yixing Xingfeng Chemical Factory) [ China (Mainland)]

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CAS No.10361-44-1 Bismuth nitrate

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Reference

Photoelectrochemical characterization of chemically deposited (CdS)X(Bi2S3)1-X composite thin films
Photoelectrochemical characterization of chemically deposited (CdS)X(Bi2S3)1-X composite thin films. Ahire, R. R.; Sankapal, B. R.; Lokhande, C. D. (Department of Physics, Thin Film Physics Laboratory, Shivaji University, Kolhapur 416 004, India). Materials Chemistry and Physics, 72(1), 48-55 (English) 2001 Elsevier Science S.A. CODEN: MCHPDR. ISSN: 0254-0584. DOCUMENT TYPE: Journal CA Section: 72 (Electrochemistry) Section cross-reference(s): 52, 76 (CdS)X(Bi2S3)1-X composite thin films were chem. deposited using simple successive ionic layer adsorption and reaction (SILAR) method onto glass and F doped Sn oxide (FTO) coated glass substrates. The films were annealed in air at 200° for 2 h and used to fabricate photoelectrochem. cells of configuration: (CdS)X(Bi2S3)1-X/Na2S-S-NaOH/C and their properties, such as current-voltage (I-V), photovoltaic output, spectral response, capacitance-voltage (Mott-Schottky plots), etc. The (CdS)X(Bi2S3)1-X composite thin films are photoactive. The effect of compn. 'X' on these properties was studied. Keywords bismuth cadmium sulfide composite photoelectrochem cell Index Entries Ceramic composites Electric capacitance-potential relationship Electric conductivity Electric current-potential relationship Flatband potential Optical absorption Photoelectrochemical cells Photovoltage photoelectrochem. characterization of chem. deposited (CdS)X(Bi2S3)1-X composite thin films 62-55-5 543-90-8 10361-44-1 in prepn. of cadmium bismuth sulfide composite 1306-23-6, uses 1310-73-2, uses 1313-82-2, uses 1345-07-9 7704-34-9, uses 7782-42-5, uses 155674-09-2 194937-69-4 376358-06-4 376358-15-5 photoelectrochem. characterization of chem. deposited (CdS)X(Bi2S3)1-X composite thin films
Surface treatment of carbon fibers
Surface treatment of carbon fibers. Hosoi, Keizo; Kominami, Naoya; Fukumi, Hirokazu; Endo, Tadayoshi (Asahi Chemical Industry Co., Ltd., Japan). Japan. Kokai JP 52040700 29 Mar 1977 Showa, 4 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: D01F011-10. APPLICATION: JP 75-116369 29 Sep 1975. DOCUMENT TYPE: Patent CA Section: 36 (Plastics Manufacture and Processing) Carbon fibers, with improved adhesion to epoxy resins, were prepd. by treating carbon fibers with aq. mixts. contg. KMnO4 [7722-64-7] and NH4 metavanadate (I) [7803-55-6] or Bi(NO3)3 [10361-44-1]. Thus, acrylic fibers were baked at 1350.degree. and the resulting carbon tow (50 g) was immersed in a mixt. of 500 mL of a permagnate compn. (contg. KMnO4 0.8, H2SO4 80.5, and H2O 18.7 parts) and 5 g I for 9 h at 120.degree. and washed. The treated fibers were embedded in a compn. contg. Epikote 828 [25068-38-6] 86, trifluoroboromonoethylamine 4, and MeCOEt 10 parts and the prepreg was heat-treated 25 min at 130.degree.. Nine resulting prepregs were molded and heat-treated 2 min at 170.degree. to give a composite with interlaminar shear strength 8.07 kg/mm2, compared with 6.28 kg/mm2 for a composite contg. fibers treated with aq. HNO3.
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