Investigation of the products of carbothermal reduction of yttrium oxide by the hydrolysis method

1984 ◽  
Vol 49 (4) ◽  
pp. 936-943 ◽  
Author(s):  
Bohumil Hájek ◽  
Pavel Karen ◽  
Vlastimil Brožek
Keyword(s):  
Yttrium Oxide ◽  
Carbothermal Reduction ◽  
Stoichiometric Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrolysis Method ◽  
Sample Decomposition ◽  
Products Of Reaction ◽  
Hydrolysis Of ◽  
Lower Carbon

For the investigation of the products of reaction of yttrium oxide with carbon mixed in various proportions, the chemical and X-ray diffraction methods of analysis were combined with the gas chromatographic analysis of the mixture of hydrocarbons and hydrogen formed on the sample decomposition with water. The carboreduction of Y2O3 was examined at relatively low temperatures, convenient for obtaining the reaction intermediates in higher yields. At 1 600 °C and pressures of 10-3 Pa the reduction of a mixture of Y2O3 with carbon in a stoichiometric ratio of 1 : 7 yields YC2 in equilibrium with 20% of Y2OC phase. At lower carbon contents (down to the Y2O3 : C ratio of 1 : 2) tha fraction of the Y2OC phase increases up to approximately 30%. In addition to Y2O3, the reaction mixture contains also Y2C, Y2OC and a phase giving propyne on hydrolysis. The presence of traces of C3 hydrocarbons and small amounts of methane in the product of hydrolysis of the carbide sample prepared by the carbothermal reduction of the oxide can be explained in terms of the occurrence of the Y15C19 phase, probably substituted in part by oxygen, and of the Y2OC phase. The results are compared with those obtained previously for the Sc2O3 + C system.

Investigation of the products of reaction of (Sc, Y)2O3 and (Sc, Dy)2O3 mixed crystals with carbon in proportions corresponding to the formation of M15C19 phase

1984 ◽  
Vol 49 (4) ◽  
pp. 944-953 ◽  
Author(s):  
Bohumil Hájek ◽  
Pavel Karen ◽  
Vlastimil Brožek
Keyword(s):  
Quantitative Phase Analysis ◽  
Stoichiometric Ratio ◽  
X Ray Diffraction ◽  
Complex Phase ◽  
Gaseous Products ◽  
Hydrolysis Method ◽  
Phase Systems ◽  
Diffraction Patterns ◽  
Products Of Reaction

Scandium, yttrium, and dysprosium formates were subjected to reaction with carbon in a stoichiometric ratio of M2O3 : C = 1 : (83/15) at 1 650 °C and 1 Pa for 40 h to give products containing typical phases of Sc2OC and Sc15C19, Y2OC and YC2, and Dy2OC and DyC2, respectively (Y2OC and Dy2OC Fm3m, a = 494.7 ± 0.2 and 495.0 ± 0.2 pm, respectively). The mixed scandium-yttrium or scandium-dysprosium carbides prepared under the same conditions did not exhibit diffraction patterns of the M15C19 carbides, and were constituted by mixed dicarbide and mixed oxide-carbide crystals. Yttrium and, to a greater extent, dysprosium are preferentially located in the dicarbide structure, whereas scandium occupies more the oxide-carbide structure. The mixed scandium-dysprosium carbide (Sc0,94Dy0,06)15C19 (P421c, a = 753 ± 1 pm, c = 1 506 ± 3 pm) starts to form at temperatures above the melting temperature of the mixture (1750-1800 °C). The composition of the gaseous products of hydrolysis is consistent with the phase composition of the samples. The method of quantitative phase analysis based on the GLC analysis of the gases evolved on the hydrolysis is employed for the analysis of complex phase systems. In addition to chemical and X-ray diffraction analysis, the hydrolysis method is also applied to the determination of additional products.

Identification of acid-insoluble filter-plugging compounds and optimal acid-washing procedures for tubular backpulse pressure filters

TAPPI Journal ◽  
2011 ◽  
Vol 10 (1) ◽  
pp. 17-23
Author(s):  
KEVIN TAYLOR ◽  
RICH ADDERLY ◽  
GAVIN BAXTER
Keyword(s):  
Calcium Sulfate ◽  
Membrane Filter ◽  
Sulfamic Acid ◽  
Xrd Analysis ◽  
Metal Sulfides ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gypsum Formation ◽  
Acid Washing ◽  
Hydrolysis Of

Over time, performance of tubular backpulse pressure filters in kraft mills deteriorates, even with regular acid washing. Unscheduled filter replacement due to filter plugging results in significant costs and may result in mill downtime. We identified acid-insoluble filter-plugging materials by scanning electron microscope/energy-dispersion X-ray spectroscopy (SEM/EDS) and X-ray diffraction (XRD) analysis in both polypropylene and Gore-Tex™ membrane filter socks. The major filter-plugging components were calcium sulfate (gypsum), calcium phosphate (hydroxylapatite), aluminosilicate clays, metal sulfides, and carbon. We carried out detailed sample analysis of both the standard acid-washing procedure and a modified procedure. Filter plugging by gypsum and metal sulfides appeared to occur because of the acid-washing procedure. Gypsum formation on the filter resulted from significant hydrolysis of sulfamic acid solution at temperatures greater than 130°F. Modification of the acid-washing procedure greatly reduced the amount of gypsum and addition of a surfactant to the acid reduced wash time and mobilized some of the carbon from the filter. With surfactant, acid washing was 95% complete after 40 min.

scholarly journals Leaching of Chalcopyrite under Bacteria–Mineral Contact/Noncontact Leaching Model

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 230
Author(s):  
Pengcheng Ma ◽  
Hongying Yang ◽  
Zuochun Luan ◽  
Qifei Sun ◽  
Auwalu Ali ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Surface Passivation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Leaching Process ◽  
Copper Leaching ◽  
Hydrolysis Of ◽  
Leaching Efficiency ◽  
Leaching Models ◽  
Scanning Electron

Bacteria–mineral contact and noncontact leaching models coexist in the bioleaching process. In the present paper, dialysis bags were used to study the bioleaching process by separating the bacteria from the mineral, and the reasons for chalcopyrite surface passivation were discussed. The results show that the copper leaching efficiency of the bacteria–mineral contact model was higher than that of the bacteria–mineral noncontact model. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier-transform infrared (FTIR) were used to discover that the leaching process led to the formation of a sulfur film to inhibit the diffusion of reactive ions. In addition, the deposited jarosite on chalcopyrite surface was crystallized by the hydrolysis of the excess Fe3+ ions. The depositions passivated the chalcopyrite leaching process. The crystallized jarosite in the bacteria EPS layer belonged to bacteria–mineral contact leaching system, while that in the sulfur films belonged to the bacteria–mineral noncontact system.

scholarly journals A Highly Selective Turn-On Fluorescent Probe for the Detection of Zinc

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3825
Author(s):  
Ling-Yi Shen ◽  
Xiao-Li Chen ◽  
Xian-Jiong Yang ◽  
Hong Xu ◽  
Ya-Li Huang ◽  
...  
Keyword(s):  
High Selectivity ◽  
Fluorescence Probe ◽  
Stoichiometric Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Turn On ◽  
Imine Nitrogen ◽  
System A ◽  
Plot Analysis ◽  
L System

A novel turn-on fluorescence probe L has been designed that exhibits high selectivity and sensitivity with a detection limit of 9.53 × 10−8 mol/L for the quantification of Zn2+. 1H-NMR spectroscopy and single crystal X-ray diffraction analysis revealed the unsymmetrical nature of the structure of the Schiff base probe L. An emission titration experiment in the presence of different molar fractions of Zn2+ was used to perform a Job’s plot analysis. The results showed that the stoichiometric ratio of the complex formed by L and Zn2+ was 1:1. Moreover, the molecular structure of the mononuclear Cu complex reveals one ligand L coordinates with one Cu atom in the asymmetric unit. On adding CuCl2 to the ZnCl2/L system, a Cu-Zn complex was formed and a strong quenching behavior was observed, which inferred that the Cu2+ displaced Zn2+ to coordinate with the imine nitrogen atoms and hydroxyl oxygen atoms of probe L.

47,49Ti NMR in Metals, Inorganics, and Gels

2000 ◽  
Vol 55 (1-2) ◽  
pp. 291-297 ◽  
Author(s):  
T. J. Bastow
Keyword(s):  
Solid State ◽  
Titanium Oxide ◽  
Recent Progress ◽  
Titanium Isopropoxide ◽  
Metallic State ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrolysis Of ◽  
C Nmr

Some recent progress in solid state 47,49Ti NMR is described and reviewed. The metallic-state work described covers metals such as hep titanium, TiB2 , a number of intermetallics such as TiAl2 and TiAl3· The inorganic work covers the various titanium oxide based materials including the TiO2 polymorphs, anatase, rutile and brookite. The gel work covers the evolution of crystalline titania from gels formed by hydrolysis of titanium isopropoxide. Some complementary data from 17O and 13C NMR and powder X-ray diffraction is also included.

Improved Enzymatic Depolymerization of Chitosan by Ionic Liquid Pretreatment and the Effect of Oligo-Chitosan on Intestinal Flora In Vitro

2011 ◽  
Vol 391-392 ◽  
pp. 1319-1323
Author(s):  
Cui Zheng ◽  
Lin Li ◽  
Hao Pang ◽  
Zhao Mei Wang ◽  
Na Li
Keyword(s):  
Ionic Liquid ◽  
Hydrogen Bonds ◽  
Molecular Hydrogen ◽  
Intestinal Flora ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hydrolysis Of ◽  
Positive Effect ◽  
Enzymatic Depolymerization

It still remains challenging for effective hydrolysis of chitosan into chitosan oligomers. In this work, a pretreatment was conducted on chitosan by an ionic liquid 1-butyl-3-methylimidazolium chloride ([C4mim]Cl), aiming at improving enzymatic depolymerization of chitosan. X-ray diffraction analysis indicated that the inter- and intra-molecular hydrogen bonds within chitosan molecules were broken by [C4mim]Cl and the crystalline was destroyed. The oligo-chitosan hydrolyzed from IL-pretreated chitosan, coded as COS-IL, showed a DP of 3~5, in contrast to DP 5~8 with oligo-chitosan obtained from untreated chitosan(coded as COS-UN). COS-IL was more effective than COS-UN in inhibiting intestinal spoilage bacterials growth and it has positive effect on the growth of intestinal probiotic bacterials.

Corrosion inhibition of N80 steel in 10% HCl + 8% HBF4solution

2019 ◽  
Vol 66 (1) ◽  
pp. 1-10
Author(s):  
Juan Du ◽  
Yuning He ◽  
Pingli Liu ◽  
Yigang Liu ◽  
Xianghai Meng ◽  
...  
Keyword(s):  
Corrosion Inhibition ◽  
Design Methodology ◽  
X Ray Diffraction ◽  
Corrosion Morphology ◽  
Content Type ◽  
X Ray ◽  
N80 Steel ◽  
Corrosion Reaction ◽  
Hydrolysis Of ◽  
Scanning Electron

PurposeThis paper aims to analyze the corrosion and corrosion inhibition of N80 in 10 per cent HCl + 8 per cent fluoroboric acid (HBF4) solution for acidizing operation.Design/methodology/approachThe corrosion rate, kinetic parameters (Ea, A) and thermodynamic parameters (ΔH, ΔS) of N80 steel in fresh acid and spent acid, 10 per cent HCl + 8 per cent HBF4, 10 per cent HCl and 8 per cent HBF4solutions were calculated through immersion tests. The corrosion and inhibition properties were studied through X-ray diffraction and electrochemical measurements. The corrosion morphology of the corrosion product was examined by scanning electron microscopy (SEM).FindingsThe results demonstrated that the spent acid was the main cause of acidification corrosion, and the HBF4would cause serious corrosion to N80 steel. The results showed that the N80 steel was more seriously corroded in the spent acid than in fresh acid, and the hydrolysis of HBF4accelerates the dissolution process of N80 steel anode to control the corrosion reaction. The results showed that the acidification will definitely cause serious corrosion to the oil tube; therefore, necessary anti-corrosion measures must be taken in the acidification process.Originality/valueThe results showed that acidizing the formation with 10 per cent HCl + 8 per cent HBF4will definitely cause serious corrosion to the oil tube, especially when the spent acid flows back. Therefore, necessary anti-corrosion measures must be taken in the acidification process, especially in the spent acid flowback stage.

CoO-Co2P composite nanosheets as highly active catalysts for sodium borohydride hydrolysis to generate hydrogen

2020 ◽  
Vol 13 (06) ◽  
pp. 2051025
Author(s):  
Hongyan Liu ◽  
Qianyu Shi ◽  
Yumei Yang ◽  
Ya-Na Yu ◽  
Yan Zhang ◽  
...  
Keyword(s):  
Sodium Borohydride ◽  
Hydrogen Generation ◽  
Sodium Hypophosphite ◽  
X Ray Diffraction ◽  
Water Displacement ◽  
X Ray ◽  
Highly Active ◽  
Naoh Solution ◽  
Adsorption Desorption ◽  
Hydrolysis Of

In this paper, CoO[Formula: see text]Co2P composite nanocatalysts as highly active catalysts were successfully prepared for catalytic hydrolysis of sodium borohydride (NaBH[Formula: see text] to generate hydrogen. For catalyst preparation, pre-synthesized Co(OH)2 nanosheets were uniformly mixed with sodium hypophosphite (NaH2PO[Formula: see text] and then treated through vapor-phase phosphorization process. For characterization, field-emission scanning electron microscopy (FE-SEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), N2 adsorption–desorption measurement and X-ray photoelectric spectroscopy (XPS) were carried out, and traditional water-displacement method was performed to measure the hydrogen generation rate (HGR). It was found that component and catalytic activity of the composites were greatly affected by the ratio of Co(OH)2 to NaH2PO2. When the ratio was 2:1, the obtained catalyst composed of CoO and Co2P presented the highest HGR up to 3.94[Formula: see text]L min[Formula: see text] g[Formula: see text] using a 2[Formula: see text]wt.% NaBH[Formula: see text][Formula: see text]wt.% NaOH solution at [Formula: see text]C, and the apparent activation energy was detected as low as 27.4[Formula: see text]kJ mol[Formula: see text]. Additionally, the optimum CoO[Formula: see text]Co2P catalyst still retains 60% of the initial activity after recycling four times.

Sign in / Sign up

Export Citation Format

Share Document