Study on the Adaptability of Alkanolamide (LDEA) Lowering Oil/Water Interfacial Tension to Different Crude Oils

In order to investigate the high interfacial activity and fair oil phase adaptability of alkanolamide, “1:1” type lauric acid diethanolamide impurities (LDEA) were synthesized and purified by the column chromatography method to obtain dodecanoic acid diethanolamide (C₁₂DEA), ester mixture, etc. The exact structures of these compounds were further confirmed by IR, gas chromatogrph with mass spectroscopy (GC–MS), and NMR. The influence of each component on the interfacial tension of oil/water (IFT) was studied by systematic quantitative analysis. The results showed that (i) the strength of each system to reduce oil/water IFT is C₁₂DEA /DEA ≈ LDEA > C₁₂DEA/DEA/ESTER > C₁₂DEA/NaOH > C₁₂DEA > C₁₂DEA/ESTER > DEA. This indicates that LDEA contributes to the reduction of the oil/water IFT and the enhanced adaptability of crude oil in this order: DEA > > ESTER; (ii) when the IFT of the LDEA/DEA system reached an ultralow value, the minimum content of DEA in the system was 1%, and the maximum ester content was less than 5% when the LDEA/DEA/ESTER system reached the ultralow IFT; (iii) the possible mechanism of effect of LDEA components on the IFT and oil phase adaptability was proposed as the synergistic process among the hydrogen bonding, alkali effect, and interface self-assembly of molecules in the interfacial layer. The contribution of these three factors were hydrogen bonding > alkali effect > interface self-assembly.     

Tunable Ni/Fe-Mo carbide catalyst with high activity toward hydrogen evolution reaction

Cost-effective catalysts for hydrogen evolution reaction (HER) are attractive for sustainable production of H₂ fuel. Herein, a series of tunable Ni/Fe-Mo carbide catalysts have been synthesized via a sol-gel method coupling with a subsequent high temperature carbonization process. The amount of nickel and iron was tuned in the Mo₇/C precursors, accomplishing a favourable performance of noble-metal-free electrocatalysts for HER. As expected, the designed Ni₁₀Fe₄Mo₇/C catalyst displays an enhanced catalytic activity toward hydrogen production with an ultralow overpotential (η₁₀ = 110 mV) and striking kinetics (η_onset = 58 mV, k = 54 mV · dec⁻¹) in the alkaline electrolyte (1 M KOH), which are comparable to those of the commercial 20% Pt/C catalyst. Such excellent performance of Ni₁₀Fe₄Mo₇/C could be attributed to the high intrinsic activities of Ni-based alloys (NiMo₄) and Mo₂C, as well as to the lattice contraction in the Mo₂C unit cell, in accordance with its high electrochemical surface area (~133 m² · g⁻¹) and low charge-transfer resistance (~31.5 Ω) for the associated electrode.     

Bonding strength and thermal shock resistance of a novel bilayer (c-AlPO4-SiCw-mullite)/SiC coated carbon fiber reinforced CMCs

Mullite coating, SiC whiskers toughened mullite coating (SiC_w-mullite), and cristobalite aluminum phosphate (c-AlPO₄) particle modified SiC_w-mullite coating (c-AlPO₄-SiC_w-mullite) were prepared on SiC coated C/SiC composites using a novel sol-gel method combined with air spraying. Results show that molten SiO₂ formed by the oxidation of SiC whiskers and molten c-AlPO₄ improved the bonding strength between mullite outer coating and SiC–C/SiC composites due to their high-temperature bonding properties. The bonding strength between mullite, SiC_w-mullite, c-AlPO₄-SiC_w-mullite outer coatings and SiC–C/SiC composites were 2.41, 4.31, and 7.38 MPa, respectively. After 48 thermal cycles between 1773 K and room temperature, the weight loss of mullite/SiC coating coated C/SiC composites was up to 11.61%, while the weight losses of SiC_w-mullite/SiC and c-AlPO₄-SiC_w-mullite/SiC coatings coated C/SiC composites were reduced to 7.40% and 5.12%, respectively. The addition of appropriate SiC whiskers can considerably improve the thermal shock resistance of mullite coating owing to their excellent mechanical properties at high temperature. In addition, c-AlPO₄ particles can further improve the thermal shock resistance of SiC_w-mullite coating due to their high-temperature bonding and sealing properties. No obvious micro-pores and cracks were observed on the surface of c-AlPO₄-SiC_w-mullite coating after 48 thermal cycles due to timely healing effect by formation of secondary mullite.     

加三角形的圈的优美性

本文研究加三角形的圈的优美性,证明了两类图 C_n(p,q,2)、C_n(p,q,3)的优美性。     

根据拉伸性能预测铝合金板材的疲劳裂纹扩展速率

本文在郑修麟和Hirt提出的疲劳裂纹扩展公式基础上’结合铝合金疲劳裂纹扩展门槛值的经验公式,提出了一个根据拉伸性能预测铝合金板材疲劳裂纹扩展速率的新方法。大量实验数据与估算结果对比表明,本文提出的疲劳裂纹扩展速率估算式是可行、实用的。此外,本文还强调了疲劳裂纹扩展门槛值△K_(th)在疲劳寿命估算中的重要性和工程中的实用性。     

羟烷基醋酸纤维素超滤膜

研究用羟烷基醋酸纤维素制成的超滤膜及其传递性质。在0.2MPa压力下,膜的截留率为92.10％～99.93％(0.05％BSA溶液),透水率为25.9～91.5ml/cm~2·h。讨论了聚合物浓度用不同官能团的有机物作第二添加剂时,其蒸发时间和凝胶介质种类,凝胶溚温度与膜性能的关系。实验结果表明,当选用能与聚合物形成氢键的有机物作第二添加剂时,由于聚合物在溶剂中的溶介能力增加可改善膜性能。     

The chemical process monitoring method based on temporal extended orthogonal neighbourhood preserving embedding (TONPE)

Due to the high dimensionality, non-linearity and dynamic characteristics of chemical process data, a fault monitoring method based on temporal extension orthogonal neighbourhood preserving embedding (TONPE) is proposed. In order to make up for the shortcomings of the orthogonal neighbourhood preserving embedding (ONPE) algorithm, an information extraction strategy based on spatio-temporal structure is developed. First, a local neighbourhood set with spatio-temporal characteristics is established, and a weight matrix with spatio-temporal is reconstructed for each time point through the nearest neighbour in space and time. Then, a projection matrix with orthogonal constraints is obtained to establish a monitoring model. The TONPE algorithm can fully capture the local dynamic changes of high-dimensional data by extracting two different manifold features, so that the low-dimensional space has better performance capabilities. The simulation results of the continuous stirred tank reactor process and the Tennessee Eastman process verify the effectiveness of the TONPE algorithm in chemical process monitoring.     

A durable and environmental friendly superhydrophobic coatings with self-cleaning,anti-fouling performance for liquid-food residue reduction

A durable and environmentally-friendly superhydrophobic coatings for liquid-food residue reduction were prepared by using stearic acid (SA) modified organic montmorillonite (SA@OMMT) and poly(dimethylsiloxane) (PDMS). Due to the natural hydrophobicity of SAs, SA@OMMT provides low surface energy as well as roughness for the coating. PDMS not only provided low surface energy in the coating but also contributed to the bonding of SA@OMMT as a result of its high adhesive properties. In addition, PDMS has good physical properties after curing, which can effectively improve the physical properties and durability of a superhydrophobic coating by the self-assembly method using a PDMS/n-hexane solution. For 1 wt.% SA@OMMT and 5 wt.% PDMS, the resulting SA@OMMT/PDMS (SOP) coating showed the water contact angle (WCA) and water sliding angle (WSA) of 156.3°and 2°, respectively. The prepared coatings have good physical and chemical stability, and they still have superhydrophobicity after physical abrasion tests and exposure to the corrosion solutions. In the meanwhile, the prepared coating also has flexibility and superhydrophobicity after bending and folding. Finally, the coating surface shows highly effective antifouling ability to liquid and solid pollutants. The coating can be applied against different substrates and has potential application in the field of liquid-food residue reduction.     

Effect of SiC whiskers on the anti-oxidation properties of Yb2Si2O7/mullite/SiC tri-layer environmental barrier coating for CMCs

The mullite and ytterbium disilicate (β-Yb₂Si₂O₇) powders as starting materials for the Yb₂Si₂O₇/mullite/SiC tri-layer coating are synthesized by a sol–gel method. The effect of SiC whiskers on the anti-oxidation properties of Yb₂Si₂O₇/mullite/SiC tri-layer coating for C/SiC composites in the air environment is deeply studied. Results show that the formation temperature and complete transition temperature of mullite were 800–1000 and 1300°C, respectively. Yb₂SiO₅, α-Yb₂Si₂O₇, and β-Yb₂Si₂O₇ were gradually formed between 800 and 1000°C, and Yb₂SiO₅ and α-Yb₂Si₂O₇ were completely transformed into β-Yb₂Si₂O₇ at a temperature above 1200°C. The weight loss of Yb₂Si₂O₇/(SiC_w–mullite)/SiC tri-layer coating coated specimens was 0.15 × 10⁻³ g cm⁻² after 200 h oxidation at 1400°C, which is lower than that of Yb₂Si₂O₇/mullite/SiC tri-layer coating (2.84 × 10⁻³ g cm⁻²). The SiC whiskers in mullite middle coating can not only alleviate the coefficient of thermal expansion difference between mullite middle coating and β-Yb₂Si₂O₇ outer coating, but also improve the self-healing performance of the mullite middle coating owing to the self-healing aluminosilicate glass phase formed by the reaction between SiO₂ (oxidation of SiC whiskers) and mullite particles.