ABSTRACT
Removal of heavy metal ions (HMIs) has attracted great attentions due to the fact that they have serious effect on environment and human beings. Manganese oxide (MnO2) was widely used as absorbent for the HMIs removal on account of its low-cost, eco-friendly and biocompatibility. The modification of morphological and structure is recognized as the effective route to improve the adsorption capacity. In this work, 2Dα-MnO2nanosheets were synthesized by hydrothermal method with Al3+additive. With the merits of high specific surface area, high dispersity in aqueous solution and abundant surface defects, 2Dα-MnO2nanosheets exhibited excellent HMIs adsorption performance. The maximum adsorption capacity of 2Dα-MnO2nanosheets reached 1.604 mmol g-1(Pb2+) and 0.813 mmol g-1(Cd2+), respectively and can maintain stable after five cycles. Besides, the established adsorption kinetics fitted well with pseudo-second-order adsorption kinetics model. Based on the above results, 2Dα-MnO2is efficient for the removal of HMIs and possesses remarkable practical application potential.
ABSTRACT
Sulfur hexafluoride (SF6), which is known as a superior electrically insulating and arc-quenching medium, plays a decisive role in the modern transmission and distribution network of electric energy, especially in high-voltage power networks. However, the ever-increasing usage of SF6 also leads to the continuous escalation of atmospheric SF6 levels, which is considered to be the main cause of the greenhouse effect. To decrease this environmental impact, eco-friendly alternatives to SF6 have been researched for decades. To date, no significant success has been made regarding replacement gases for transmission networks. Some potential alternatives have comparatively lower global warming potential (GWP) but involve technical trade-offs. Thiazyl trifluoride, which has some excellent chemical and electric properties, is a novel substitution candidate for SF6. In this article, an efficient synthetic route starting from sulfur monochloride and followed by ammonization and fluorination was proposed. The structures of the intermediates and the target products were determined by X-ray diffraction (XRD), infrared spectroscopy (IR), and gas chromatography-mass spectrometry (GC-MS). The effects of some determining factors on the yield and purity, including the molar ratio of the reactants, recrystallization conditions and condensation temperature, were also investigated. The results showed that the overall yield of thiazyl trifluoride was approximately 25%, while the purity could be up to 90.6% under optimal conditions.
ABSTRACT
A novel and efficient preparation route of insulating gas-heptafluoroisobutyronitrile was developed. The synthetic route involved halogen-exchange fluorination, decomposition of bis-(perfluoroisopropyl) ketone and dehydration reaction. Overall, the desired compound was produced without the use of extremely toxic and expensive substances. Structures of the as-obtained products were determined by 19F NMR, 13C NMR, IR and GC-MS. The effects of several variables on reaction yield including nature of potassium fluoride, the catalyst dosage, temperature, solvent and molar ratio of raw materials were all investigated. The results indicated that the total yield of heptafluoroisobutyronitrile could reach 42% from original materials under optimal conditions and the mechanism of the reaction was proposed.
ABSTRACT
A novel synthetic route to perfluoroisobutyronitrile from perfluoroisobutyryl acid which has mild conditions and low toxicity is described. This study introduces detailed synthetic protocols and characterization including GC-MS, 13C NMR and 19F NMR spectroscopy of perfluoroisobutyryl acid, perfluoroisobutyryl chloride, perfluoroisobutyl amide and perfluoroisobutyronitrile. Besides, this route is superior to the established patent and shows potential application in high voltage electrical equipment.
