不锈钢在湿法磷酸中的应用

介绍湿法磷酸生产中杂质、操作条件、酸浓度、温度、搅拌、有饥物等对腐蚀的影响和材料选择的基本要素，并列出多种不锈钢的主要化学成份和几种工艺流程的材料选用表。     

不锈钢在湿法磷酸中腐蚀行为研究

本文采用腐蚀实验和电化学测试方法对不锈钢在湿法磷酸中的腐蚀行为进行了研究，并进行钝化膜的组成与结构分析。研究表明，磷酸中加入ＳＯ４＾２＾－，ｃＬ＾－，Ｆ＾－均提高合金的维钝电流密度和致纯电流浓度，加速材料的腐蚀，这些杂质共存时腐蚀性更大。湿法磷酸中存在的Ｓｉ＾４＾＋，Ａｌ＾３＾＋，Ｍｇ＾２＾＋和Ｆｅ＾３＾＋起缓蚀作用。不锈钢纯化膜主要由Ｃｒ和Ｆｅ的氧化物组成，表面形成致密稳定的Ｃｒ２Ｏ３保护膜是提     

间二甲苯-磷酸-水三元体系的液-液相平衡

实验测定了不同温度下,间二甲苯-水二元体系和间二甲苯-磷酸-水三元体系的液-液相平衡数据。研究了磷酸中的杂质Fe~(3+)、Al~(3+)和Mg~(2+)对间二甲苯-磷酸-水三元体系相平衡的影响,以及杂质在两相中的分配情况。研究结果对共沸精馏浓缩磷酸提供了必要的理论依据和基础数据。     

Recovery of Phosphoric Acid from Spent Petrochemical Catalysts

Petrochemical catalysts are widely used in the industry. For the production of cumene, zeolite-based catalysts containing phosphoric acid are applied. Over the time, coking deactivates the surface, and the catalyst has to be exchanged and disposed of. Different process approaches for recycling the phosphoric acid-containing catalysts were investigated. Related preliminary investigations have shown that calcination of the used catalyst is necessary prior to reprocessing. By digesting the catalyst with hydrofluoric acid, ∼96 % phosphate was recovered. However, this process is very costly in terms of process technology. More promising is digestion by basic or acidic routes. Several options are possible here, and digestion with H₃PO₄ proved to be particularly suitable. Here, phosphate yields reached up to 98.8 %, with a positive balance of economic efficiency at the same time. The catalyst can be produced and recycled in the same plant with the same reagents, what constitutes a major breakthrough towards sustainability in industrial catalysis.     

Alpha-hydroxy glycolic acid for root dentin etching: Morphological analysis and push out bond strength

The purpose of this study was investigated the use of α-hydroxy glycolic acid as a dentin etchant for adhesive procedures in the root canal. The etching pattern of glycolic acid and mineral content distribution of root canal dentin were assessed by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS), respectively. The effect of glycolic acid surface etching on the push out bond strength of fiber post to root dentin was assessed using three adhesive systems: Single Bond Universal [SBU], Scotchbond Multipurpose [SBMP], and Ambar [AM]. The 37% phosphoric acid was used as a control group. The bond strength values were statistically compared using ANOVA/Fisher LSD tests (α = 0.05). SEM revealed similar etching patterns for phosphoric acid and glycolic acid. Both acids also shared similar interfacial morphology of the hybrid layer. EDS showed similar levels of Ca and Mg after treatment with glycolic acid when compared with phosphoric acid. When the P level was compared, it was observed that phosphoric acid caused greater removal of P. The push out bond strengths were statistically similar between glycolic acid and phosphoric acid in all groups (p > 0.05). Comparisons using post hoc Fisher LSD test showed that the bond strengths in the SBU and SBMP groups were not significantly different from each other (p > 0.05). The bond strength in the AM group was similar to that in the SBMP group (p > 0.05); however, it was significantly lower than that in the SBU group (p < 0.05). It can be concluded that the glycolic acid effectively etched root dentin surfaces, resulting in a surface pattern, hybrid layer, and push out bond strength similar to those produced by traditional phosphoric acid. Therefore, glycolic acid may be recommended as a suitable root dentin surface etchant for adhesive restorative procedures.     

Photoluminescence emission of nanoporous anodic aluminum oxide films prepared in phosphoric acid

The photoluminescence emission of nanoporous anodic aluminum oxide films formed in phosphoric acid is studied in order to explore their defect-based subband electronic structure. Different excitation wavelengths are used to identify most of the details of the subband states. The films are produced under different anodizing conditions to optimize their emission in the visible range. Scanning electron microscopy investigations confirm pore formation in the produced layers. Gaussian analysis of the emission data indicates that subband states change with anodizing parameters, and various point defects can be formed both in the bulk and on the surface of these nanoporous layers during anodizing.     

Electrochemical hydrogen pumping using a high-temperature polybenzimidazole (PBI) membrane

Electrochemical hydrogen pumping using a high-temperature (>100 °C) polybenzimidazole (PBI) membrane was demonstrated under non-humidified and humidified conditions at ambient pressures. Relatively low voltages were required to operate the pump over a wide range of hydrogen flow rates. The advantages of the high-temperature capability were shown by operating the pump on reformate feed gas mixtures containing various amounts of CO and CO₂. Gas purity measurements on the cathode gas product were conducted and significant reductions in gas impurities were detected. The applicability of the PBI membrane for electrochemical hydrogen pumping and its durability under typical operating conditions were established with tests that lasted for nearly 4000 h.     

高效液相色谱/质谱联用测定保健食品中的伐地那非

为测定保健食品中伐地那非，建立了高效液相色谱质谱联用（HPLC—ES／MS）的测定方法。该方法以紫外定量，质谱定性。色谱条件为RP—C18色谱柱，流动相：0．2％甲酸水溶液＋乙腈=65＋35（体积分数）；流速1ml／min；进样量5μl；检测波长254nm。质谱采用电喷雾正离子模式（ESI＋），扫描范围为：200-700（m/z）。伐地那非在3．6—450μg/ml范围内，浓度与峰面积呈良好的线性关系，定量检出限为18ng，最低检出限为0．9ng（S/N=6）。本方法流动相简单，分析时间短且试样预处理简单，灵敏度高，借助质谱的定性能力，可大大提高方法可靠性和抗干扰能力，能准确快速地测定保健食品中的伐地那非。     

Effects of temperature and phosphoric acid addition on the solubility of iron phosphate dihydrate in aqueous solutions

As important controlling factors for the synthesis of iron phosphate materials by liquid-phase precipitation, the solubilities of iron phosphate dihydrate were systematically measured at H_3PO_4 concentrations from 1.13 wt%to 10.7 wt%, temperature from 298.15 to 363.15 K, and atmosphere pressure in this work. The solubility was found to increase 5 orders of magnitude or more with increasing the concentration of phosphoric acid, and decrease 1 to 2 orders of magnitude with increasing the equilibrium temperature. The phosphoric acid addition and temperature were found to affect the solubility of iron phosphate dihydrate by the formation or dissociation of coordination species, which could further accelerate the phase transformation from the amorphous iron phosphate dihydrate to orthorhombic iron phosphate dehydrate by dissolution–recrystallization mechanism.The high dependences of the solubility of iron phosphate materials on H_3PO_4 concentration and temperature were also well predicted by calibration equations, which are meaningful for quantitatively understanding the precipitation process and sequential crystalline structure transformation and pursuing a rational strategy for synthesizing specific iron phosphate materials.     

Effect of phosphoric acid on the performance of low antimony grid of Pb‐acid cell under constant current charging and discharging

Effect of phosphoric acid on the performance of Pb‐1.7%Sb grid of lead‐acid cell is studied in 5 M H₂SO₄ by cyclic galvanostatic polarization and impedance spectroscopy. An increase in capacitance to a maximum is recorded during the initial stages of the electro‐reduction of PbO₂ into Pb(II) compounds and attributed to concurrent compositional and dimensional changes. These changes include removal of O₂ bubbles, insertion of large amounts of H₂SO₄ and H₂O. Efficiency of PbO₂ formation decreases, while its rate of self‐discharge increases with increasing the charging current and in the presence of H₃PO₄. The charge capacity increases with increasing the discharging current due to the decrease in the self‐discharge. The charge capacity is lower in the presence of H₃PO₄. On increasing the cycle number, the corrodibility of the grid increases, because more layers of the surface Pb are involved in the self‐discharge. H₃PO₄ significantly retards the effect of cycle number.