Electrical and optical properties of fluorine-doped CdO films deposited by ultrasonic spray pyrolysis

The CdO:F samples have been deposited onto microscope glass substrates at 250 °C by ultrasonic spray pyrolysis method. With the incorporation of fluorine into CdO, the direct optical transition has shifted towards the shorter wavelengths, and the transparency of the material has increased at a given wavelength above the fundamental absorption edge. The shift in the absorption edge is explained by means of the Moss–Burstein effect, which is also supported with the results of the current–voltage characteristics. Here, a correlation has been established between the band broadening and the increase in conductivity due to the increase in carrier density.     

微波高压提取快速测定饲料含氟量的探讨

采用微波高压制样技术,快速提取饲料中的氟元素,结合氟离子选择性电极标准添加和电位极差测试方法,能够快速、准确地测试饲料中的含氟量     

Performance of fluorine-added CoMoS/Al2O3 prepared by sonochemical and chemical vapor deposition methods in the hydrodesulfurization of dibenzothiophene and 4,6-dimethyldibenzothiophene

The performance of a new type of CoMoS/Al₂O₃ catalyst, with added fluorine and prepared by sonochemical and chemical vapor deposition (CVD) methods, was investigated in the hydrodesulfurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT). The catalyst, which was designed to contain optimum amounts of fluorine and cobalt, exhibited a higher activity, ca. 4.6 times higher activity particularly in the HDS of 4,6-DMDBT, than a fluorine-free catalyst prepared by a conventional impregnation method. The enhanced activity of the new catalyst can be attributed to the cumulative effects of individual factors involved in the catalyst preparation. That is, the use of a sonochemical synthesis led to a high dispersion of small MoS₂ crystallites on the alumina, and the addition of the Co species to the catalyst by CVD caused a close interaction between the Co species and the MoS₂ crystallites to produce numerous CoMoS species, which are the catalytically active species for HDS. The addition of fluorine increased the amounts of acidic sites in the catalyst, which promoted hydrogenation (HYD) route to a greater extent than the direct desulfurization (DDS) route in DBT HDS and both HYD and DDS routes to similar extents in the case of 4,6-DMDBT HDS. Accordingly, the addition of fluorine led to a greater increase in catalytic activity for 4,6-DMDBT HDS than for DBT HDS.     

Fate of the chlorine and fluorine in a sub-bituminous coal during pyrolysis and gasification

The fate of the chlorine and fluorine present in a sub-bituminous coal from Indonesia during pyrolysis and gasification has been studied with fixed and entrained bed reactors. The rate profile for HCl evolved in the temperature programmed pyrolysis exhibits the main and shoulder peaks at 480 and 600 °C, respectively. Model experiments and subsequent Cl 2p XPS measurements show that HCl reacts with metal impurities and carbon active sites at 500 °C to be retained as inorganic and organic chlorine forms, from which HCl evolves again at elevated temperatures. It is suggested that the HCl observed in the coal pyrolysis may originate from the above-mentioned chlorine functionalities formed by secondary reactions involving the nascent char. In the CO₂ gasification of the 900 °C char at 1000 °C and 2.5 MPa, any measurable amounts of HCl and HF could not be detected even at a high conversion of 75 wt% (daf), suggesting the accumulation of these halogens in the residual char. When the coal is injected into an O₂-blown, entrained bed gasifier at 1200-1400 °C under 2.6 MPa, the partial oxidation proceeds to a larger extent at a higher O₂/coal ratio, whereas the chlorine and fluorine are enriched in the remaining char, and the extent of the enrichment at the latter stage of gasification is larger with the fluorine. The XPS measurements of the chars reveal the presence of the broad F 1 s peak, which can cover a wide range of binding energies attributable to inorganic and organic fluorine. The halogen enrichment during gasification is discussed in terms of secondary reactions of HCl and HF with char.     

核壳型含氟丙烯酸酯共聚乳液

以十二烷基硫酸钠（SDS）和壬基酚聚氧乙烯基醚（OP-10）为复合乳化剂，甲基丙烯酸十二氟庚酯（Actyflon-God）、甲基丙烯酸甲酯（MMA）、丙烯酸丁酯（BA）为原料制备了壳层含氟的核壳型丙烯酸酯共聚物乳液。用红外光谱（FT—IR）表征乳胶膜化学组成，用透射电子显微镜（TEM）观察了乳胶粒的微观形态结构，并用X射线光电子能谱（XPS）进行了表面分析。发现氟有向空气与膜面迁徙的现象。通过吸水率表征含氟丙烯酸酯共聚物乳胶膜的表面性能，结果表明含氟量增加使乳胶膜吸水率大大降低。     

Synthesis of fluorine-graphite intercalation compounds by elemental fluorine and high oxidation-state transition-metal fluorides

Fluorine-graphite intercalation compounds have been synthesized using high purity fluorine gas and high oxidation-state transition-metal fluorides, AgF₃ and NiF₃, at room temperature and at −78 °C. At room temperature, a mixture of stage 1 + 2 − 4 compounds with compositions, C_4.2F to C_14.6F were obtained. On the other hand, stage 2–4 compounds with compositions C_5.6F to C_14.2F were synthesized at −78 °C. The fluorinating ability of AgF₃ and NiF₃ has been shown more clearly at room temperature because a small amount of fluorine was intercalated/absorbed into graphite at −78 °C without catalysts. XPS spectra show that ionic, nearly ionic, semi-covalent and covalent fluorines coexist in the C_xF samples, and that the covalency of CF bonding increases with decreasing stage number.     

新型无氟发泡工艺技术改进

介绍了传统无氟发泡工艺具体工况,分析了聚氨酯泡沫存在容易产生形变、强度和韧性不高和工艺中附加物分散性不佳等问题,本文提出一种改进的无氟发泡工艺,与传统的无氟发泡工艺相比,改进的无氟发泡工艺能有效解决聚氨酯泡沫易形变的问题,提高了聚氨酯的强度及韧性,增加了附加物的分散性效果,降低了发泡体系设备.对进一步改善无氟发泡工艺技术具有重要意义.     

Effect of α-substituents on molecular motion and wetting behaviors of poly(fluoroalkyl acrylate) thin films with short fluoroalkyl side chains

The effect of α-substituent on the molecular motion and wetting behavior of poly{2-(perfluorobutyl)ethyl acrylate} [PFA-C₄], poly{2-(perfluorobutyl)ethyl methacrylate} [PFMA-C₄], poly{2-(perfluorobutyl)ethyl α-fluoroacrylate} [PFFA-C₄], and poly{2-(perfluorobutyl)ethyl α-chloroacrylate} [PFClA-C₄] films were characterized by dynamic contact angle measurement, lateral force microscopy (LFM), wide angle X-ray diffraction (WAXD), and X-ray photoelectron spectroscopy (XPS). WAXD of oriented PFClA-C₄ fiber suggested the presence of rod-like chain due to the presence of bulky α-substituent. The glass transition temperature (T_g) of PFFA-C₄ and PFClA-C₄ were well above the room temperature. The water repellencies of PFFA-C₄ and PFClA-C₄ were as high as that of PFMA-C₄ and their oil repellency of PFFA-C₄ and PFClA-C₄ was higher than the PFMA-C_4. This result was originated from the low main chain mobility of PFFA-C₄ and PFClA-C₄ due to the presence of bulky α-substituents. The effect of molecular motion on water repellency was clarified by the results of temperature dependence studies of dynamic contact angle, LFM, and surface chemical composition measured by XPS.     

The effect of fluorine content on the mechanical properties of poly (?-caprolactone)/nano-fluoridated hydroxyapatite scaffold for bone-tissue engineering

In this study, the effect of fluorine content on the mechanical properties of the novel poly (?-caprolactone)/nano-fluoridated hydroxyapatite nanocomposite scaffolds was investigated. Poly (?-caprolactone)/nano-fluoridated hydroxyapatite (PCL-FHA) scaffolds were produced by solvent casting/particulate leaching method. The fluoridated hydroxyapatite nanopowders had a chemical composition of Ca₁₀(PO₄)₆OH_2−xF_x (where x values were selected equal to 0.5, 1, 1.5 and 2.0). Various weight percentages (10, 20, 30 and 40) of the FHA were added to the PCL. Sodium chloride (NaCl) particles having diameter of 300-500 μm were used as porogen. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR) were used to identify the phase structure and functional groups of obtained scaffolds. Mechanical properties of the prepared scaffolds were also determined. Results showed that the compressive strength of scaffolds increases with decreasing the weight percent of fluorine in FHA.     

某金矿氟石膏基新型膏体充填材料配比试验研究

基于目前水泥胶凝材料价格大幅上调导致膏体充填成本高昂的实际境况,为降低充填成本,以工业废弃氟石膏为主要研究对象进行相关研究。利用氟石膏代替水泥,结合废石、粉煤灰、生石灰等掺加料,并辅以一定量的添加剂,开展氟石膏基新型膏体充填材料配比试验研究。通过坍落度、扩展度等试验确定材料的最优配比,并对膏体进行单、三轴及SEM试验,分析其宏微观结构。研究结果表明：质量浓度增大0min至120min,坍落度、扩展度损失率随之增大,泌水率却逐渐减小;最优配比所制成氟石膏基膏体的单轴压缩应力—应变曲线属于弹塑性曲线,最高可达6~7MPa;单轴与三轴压缩试验后,膏体表面未出现大的破裂面,且随围压的增加,应力—应变曲线不再出现峰值应力;所制充填材料的水化物主要包括钙矾石（AFt）、水化硅酸钙凝胶（C-S-H凝胶）和二水硫酸钙（CaSO4?2H2O）。氟石膏基新型膏体充填材料的配制具有深远的影响,为实现高效安全、绿色可持续的矿山开采提供了保障。