Ammonium Hydrogen Difluoride

Keyword(s):  
2021 ◽  
Vol 48 ◽  
pp. 45-53
Author(s):  
Agnieszka Defus ◽  
Elena Possenti ◽  
Antonio Sansonetti ◽  
Cristina Tedeschi ◽  
Chiara Colombo ◽  
...  

1977 ◽  
Vol 66 (12) ◽  
pp. 5433-5438 ◽  
Author(s):  
E. K. Wolff ◽  
R. G. Griffin ◽  
C. Watson

CrystEngComm ◽  
2005 ◽  
Vol 7 (44) ◽  
pp. 276 ◽  
Author(s):  
Dario Braga ◽  
Marco Curzi ◽  
Matteo Lusi ◽  
Fabrizia Grepioni

2007 ◽  
Vol 124-126 ◽  
pp. 1765-1768 ◽  
Author(s):  
So Yeon Lee ◽  
Yong Kul Lee ◽  
S.Ted Oyama ◽  
Seok Hee Lee ◽  
Hee Chul Woo

Silica supported nickel molybdenum phosphides (NiMoP/SiO2) were successfully prepared by temperature-programmed reduction (TPR) reaction of phosphorous-impregnated nickel molybdenum oxides (NiMoO4) precursors with hydrogen at relatively low temperatures (530 – 590 oC) and characterized by Fourier transform-Infrared spectrometry (FT-IR), X-ray diffraction (XRD), Electron probe microanalysis (EPMA) and Temperature-programmed reduction reaction (TPR). The process of solid transformation and properties of materials prepared from ammonium hydrogen phosphate (AMP)-impregnated samples were compared with those of phosphide made from phosphoric acid (PAC)-impregnated samples. Results show that the formation of a single NiMoP phase on silica significantly depends on reduction rates, phosphorous sources and phosphorous loadings. A single phase of NiMoP on SiO2 was particularly promoted at a below 5 oC/min of reduction rate and the starting molar ratio of Ni/Mo/P=1/1/1. A single phase of crystalline NiMoP on silica was produced from AMP-impregnated samples, while other phases of MoP, Ni2P, or NiMoP2 were appeared from PAC-impregnated samples with loading. The new phase of NiMoP2 was occurred with increasing phosphorous loading (above Ni/Mo/P=1/1/2.5) as a result of facilitated contact on the surface between the Ni-Mo bimetallic component and the phosphorous reagent


2020 ◽  
Vol 7 (1) ◽  
pp. 6
Author(s):  
Dianjun Hu ◽  
Xin Liu ◽  
Ziyu Liu ◽  
Xiaoying Li ◽  
Feng Tian ◽  
...  

As a kind of promising material for a Faraday isolator used in the visible and near infrared range, Dy2O3 transparent ceramics were prepared by vacuum sintering from the nano-powders synthesized by the liquid precipitation method using ammonium hydrogen carbonate as precipitant with no sintering aids. The synthesized precursor was calcinated at 950 °C–1150 °C for 4 h in air. The influences of the calcination temperature on the morphologies and phase composition of Dy2O3 powders were characterized. It is found that the Dy2O3 powder calcinated at 1000 °C for 4 h is superior for the fabrication of Dy2O3 ceramics. The Dy2O3 transparent ceramic sample prepared by vacuum sintering at 1850 °C for 10 h, and subsequently with air annealing at 1400 °C for 10 h, from the 1000 °C-calcined Dy2O3 powders, presents the best optical quality. The values of in-line transmittance of the optimal ceramic specimen with the thickness of 1.0 mm are 75.3% at 2000 nm and 67.9% at 633 nm. The Verdet constant of Dy2O3 ceramics was measured to be −325.3 ± 1.9 rad/(T·m) at 633 nm, about 2.4 times larger than that of TGG (Tb3Ga5O12) single crystals.


Author(s):  
Sameer Amereih ◽  
Thomas Meisel ◽  
Wolfhard Wegsheider

Two independent digestion techniques (microwave acid digestion with HF and HCl, HNO3 and Na2O2 sintering, respectively) were applied to determine the total Sb concentration in a real soil sample and in reference materials: Icelandic Basalt (BIR-1), Cody Shale (SCo-1) and (Soil-7). ICP-MS was used to determine total antimony concentrations in the digested and the extracted solutions using external calibration and isotope dilution technique. The recoveries of Sb using HF in the acids digestion mixture in closed-vessels microwave digestion system were excellent and the concentrations are in very good agreement with certified or reported concentrations of reference materials. Using closed-vessels combined with microwave heating systems probably prevents the loss of volatile Sb compounds. The use of hydrogen fluoride with other strong acid can help dissociating insoluble antimony silicates. Different extraction reagents were tested for their ability to extract antimony using an ultrasonic bath namely: EDTA disodium salt, potassium hydroxide, citric acid monohydrate, pyridine-2,6-dicarboxylic acid, ammonium acetate, ammonium oxalate, ammonium thiocyanate, ammonium persulphate and di-ammonium hydrogen citrate. A 500 mmol L-1 solution of citric acid pH 1.08 proved to be the most efficient extractant. Optimization of the extraction conditions were investigated by studying the effect of pH, concentration, temperature, time of extraction, the ratio of sample mass to the volume of extractant and the number of consecutive extractions. As a result three consecutive extractions for a total time of 45 min at 80 ˚C was the most efficient condition for Sb extraction. Using these extraction conditions 61%, 3.7% RSD and 42%, 2.2% RSD (n=6) of the total antimony in the real soil and Soil-7 samples, respectively could be extracted.


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