scholarly journals Determination of Three-Dimensional Morphology and Inner Structure of Second-Phase Inclusions in Metals by Non-Aqueous Solution Electrolytic and Room Temperature Organic Methods

Metals ◽  
2018 ◽  
Vol 8 (1) ◽  
pp. 68 ◽  
Author(s):  
Jing Guo ◽  
Keming Fang ◽  
Hanjie Guo ◽  
Yiwa Luo ◽  
Shengchao Duan ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Room Temperature ◽  
Three Dimensional ◽  
Second Phase

scholarly journals Identification of an Al–Ni–O precipitate in combustion-synthesized NiAl

2000 ◽  
Vol 33 (5) ◽  
pp. 1217-1222
Author(s):  
A. Biswas ◽  
Madangopal K. ◽  
J. B. Singh ◽  
S. K. Roy ◽  
S. Banerjee
Keyword(s):  
Room Temperature ◽  
Point Group ◽  
Composition Analysis ◽  
Second Phase ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Phase Precipitate ◽  
Transmission Electron ◽  
Chemical Composition Analysis

The complete identity of a second-phase precipitate detected by transmission electron microscopy in combustion-synthesized NiAl was established. The crystal structure, including the point group, the space group and the lattice parameters, was determined by convergent and selected-area electron diffraction techniques. Energy dispersive X-ray spectroscopy was used for the determination of the chemical composition. Analysis established the phase to be the solid solution of NiO in Al2O3and presented evidence of the hitherto unreported room-temperature solubility.

Structural Systematics of Rare Earth Complexes. XXII. ('Maximally') Hydrated Rare Earth Iodides

2000 ◽  
Vol 53 (10) ◽  
pp. 867 ◽  
Author(s):  
Kevin C. Lim ◽  
Brian W. Skelton ◽  
Allan H. White
Keyword(s):  
Aqueous Solution ◽  
Rare Earth ◽  
Low Temperature ◽  
Single Crystal ◽  
Room Temperature ◽  
Second Phase ◽  
X Ray ◽  
Structure Determinations ◽  
Trivalent Rare Earth ◽  
Trigonal Prismatic

Low-temperature (c. 153 K) single-crystal X-ray structure determinations, carried out on trivalent rare earth iodides crystallized from aqueous solution at room temperature, have defined two series of hydrates, LnI3.nH2O. For Ln = La–Ho, a nonahydrate phase (n = 9) is defined, orthorhombic Pmmn, a ~ 11.5, b ~ 8.0, c ~ 8.8 Å, Z = 2, the second phase (n = 10), monoclinic P21/c, Z = 4 being defined for Ln = Er–Lu, a ~ 8.2, b ~ 12.8, c ~ 17.1 Å, β ~ 103.7˚. Neither of these phases is isomorphous with any of those pertinent to the previously studied chloride or bromide (hydrated) arrays, nor, unlike those, does the halide (iodide) in any case enter the coordination sphere of the lanthanoid. The n = 9 phase takes the form [Ln(OH2)9]I3, the nine-coordinate lanthanoid environment stereochemistry being tricapped trigonal-prismatic, while the n = 10 phase is [Ln(OH2)8]I3.2H2O, the eight-coordinate lanthanoid environment being square-antiprismatic.

Simple Colorimetric Method for Determination of Metaproterenol Sulfate in Pharmaceuticals

1984 ◽  
Vol 67 (1) ◽  
pp. 137-138
Author(s):  
Ramesh T Sane ◽  
Satish V Sawant ◽  
Vipul J Doshi ◽  
Jagannath G Mhalas ◽  
Ajay K Paarikh ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Room Temperature ◽  
Colorimetric Method ◽  
Statistical Validation

Abstract A simple coiorimetric method is described for the determination of metaproterenol sulfate (orciprenaline sulfate). The method is based on measurement of a colored species formed when metaproterenol sulfate is treated with diazotized dapsone, p-nitroaniline, or benzocaine at room temperature, followed by treatment with an aqueous solution of trimethylamine in the case of benzocaine. Compounds such as starch, talc, and common excipients do not interfere in the reaction. Statistical validation showed that the method was precise and accurate. The results agree well with those obtained by other methods reported in the literature.

Darstellung, Schwingungsspektren und Normalkoordinatenanalysen der Dioxoosmate(VI) trans-[OsO2(CN)2(ox)]2-, transs-[OsO2(CN)2(mal)]2- und trans-[OsO2(CN)2(N2H2C2O2)]2- / Synthesis, Vibrational Spectra and Normal Coordinate Analysis of the Dioxoosmates(VI) frans-[OsO2(CN)2(ox)]2- , trans-[OsO2 (CN)2(mal)]2- and trans-[OsO2 (CN)2(N2H2C2O2)]2-

1999 ◽  
Vol 54 (9) ◽  
pp. 1116-1121
Author(s):  
A. Strueß ◽  
W. Preetz
Keyword(s):  
Aqueous Solution ◽  
Oxalic Acid ◽  
Raman Spectra ◽  
Malonic Acid ◽  
Vibrational Spectra ◽  
Room Temperature ◽  
Normal Coordinate ◽  
X Ray ◽  
Ir And Raman

By careful acidification of the aqueous solution of trans-K2[OsO2(OH)4] in the presence of the required amount of cyanide ions with oxalic acid, malonic acid or oxamide the osmyl complexes trans-[OsO2(CN)2(ox)]2- (1), trans-[OsO2(CN)2(mal)]2- (2) und trans-[OsO2(CN)2(N2H2C2O2)]2- (3) are formed. The IR and Raman spectra of the (n-Bu4N) and (Et4N) salts of 1, 2 und 3 were measured at room temperature. Based on the molecular parameters of the X-ray determination of related complexes normal coordinate analyses have been performed and the vibrations were assigned. The valence force constants are fd(C≡N ) = 16.95, fd(Os=O) = 6.68 - 6.70, fd(Os-O) = 2.55 - 2.60, fd(Os-C) = 2.55 and fd(Os-N) = 2.30 mdyn/Å. For the chelate ligands, fd(C =0) ranges from 11.03 - 11.15, fd(C-O/N) from 4.86 - 5.05 and fd(C-C) from 4.07 - 4.70 mdyn/Å.

Simple Colorimetric Method for Determination of Pyridoxine Hydrochloride (Vitamin B6) in Pharmaceuticals

1983 ◽  
Vol 66 (1) ◽  
pp. 158-160
Author(s):  
Ramesh T Sane ◽  
Vipul J Doshi ◽  
Sanjay K Joshi
Keyword(s):  
Aqueous Solution ◽  
Sulfuric Acid ◽  
Vitamin B6 ◽  
Trichloroacetic Acid ◽  
Room Temperature ◽  
Colorimetric Method ◽  
Thiamine Hydrochloride ◽  
Pyridoxine Hydrochloride ◽  
Statistical Validation

Abstract A simple colorimetric method is described for the determination of pyridoxine hydrochloride (vitamin B6). The method is based on the measurement of an orange species formed when pyridoxine hydrochloride is treated with diazotized dapsone and sulfanilamide in a mixture of trichloroacetic acid and sulfuric acid at room temperature, followed by treatment with an aqueous solution of sodium carbonate. Compounds such as thiamine hydrochloride, cyanocobalamin, and common excipients such as starch and talc which are present in various formulations with pyridoxine hydrochloride do not interfere in the reaction. Statistical validation showed that the method was highly precise and accurate. Results agree well with those obtained by other methods reported in the literature.

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