Microstructure and hydrogen storage properties of Ti–V–Cr based BCC-type high entropy alloys

In this work, the crystal structure and hydrogen storage properties of V₃₅Ti₃₀Cr₂₅Fe₁₀, V₃₅Ti₃₀Cr₂₅Mn₁₀, V₃₀Ti₃₀Cr₂₅Fe₁₀Nb₅ and V₃₅Ti₃₀Cr₂₅Fe₅Mn₅ BCC-type high entropy alloys have been investigated. It was found that high entropy promotes the formation of BCC phase while large atomic difference (δ) has the opposite effect. Among the four alloys, the V₃₅Ti₃₀Cr₂₅Mn₁₀ alloy shows the highest hydrogen absorption capacity while the V₃₅Ti₃₀Cr₂₆Fe₅Mn₅ alloy exhibits the highest reversible capacity. The cause of the loss of desorption capacity is mainly due to the high stability of the hydrides. The higher room-temperature desorption capacity of the V₃₅Ti₃₀Cr₂₅Fe₅Mn₅ alloy is due to higher hydrogen desorption pressure. After pumping at 400 °C, the hydrides can return to the original BCC structure with only a small expansion in the cell volume.     

Hydrogen production from thermal decomposition of ammonia-contaminated acid gas using a detailed reaction mechanism

The increase in the production of acid gas consisting of H₂S, CO₂, and associated impurities such as ammonia and hydrocarbons from oil and gas plants and gasification facilities has stimulated the interest in the development of alternative means of acid gas utilization to produce hydrogen and sulfur, simultaneously. The present literature lacks a detailed reaction mechanism that can reliably predict the thermal destruction of NH₃ and its blend with H₂S and CO₂ to facilitate process optimization and commercialization. In this paper, a detailed mechanism of NH₃ pyrolysis is developed and is merged with the reactions of NH₃ oxidation and H₂S/CO₂ thermal decomposition from our previous works. The mechanism is validated successfully using different sets of experimental data on the pyrolysis and oxidation of NH₃, H₂S, and CO₂. The proposed mechanism predicts the experimental data on NH₃ pyrolysis remarkably better than the existing mechanisms in the literature. The mechanism is used to investigate the effects of NH₃ concentration (0–20%) and reactor temperature (1000–1800 K) on the thermal decomposition of H₂S and CO₂. A synergistic effect is observed in the simultaneous decomposition of NH₃ and CO₂, i.e., NH₃ conversion is improved in the presence of CO₂ and the decomposition CO₂ to CO is enhanced in the presence of NH₃. The presence of H₂S suppressed NH₃ conversion, while the conversion of H₂S remained unchanged with increasing NH₃ concentration at temperature below 1400 K due to the low conversion of NH₃ (up to 18%). At temperature above 1400 K, NH₃ conversion increased rapidly and it triggered a decrease in H₂S conversion as well as the yields of H₂ and S₂. The major reactions involved in the decomposition of H₂S, CO₂, and NH₃ and the production of major products such as H₂, S₂, and CO are identified. The detailed reaction mechanism can facilitate the design and optimization of acid gas thermal decomposition to produce hydrogen and sulfur, simultaneously.     

Modification of pork-skin jelly by enzymatic cross-linking: melting resistance and quality improvement

Improvements of melting resistance and quality by modification of pork-skin jelly through enzymatic cross-linking were studied, and the mechanism of quality improvement was discussed in this work. Gel strength, springiness and chewiness of modified gel increased significantly (P < 0.05). Transglutaminase (TGase) also improved the viscoelasticity, stability and melting resistance of gel system, as proved by rheological analysis. Sensory evaluation showed that increase in texture need to be moderate and the utilisation of 0.6% TGase was the most appropriate for pork-skin jelly. Significant effects of TGase on inducing protein cross-link and aggregation were confirmed by determining rheology during enzyme treatment and cross-linking extent of pork-skin soup. Correlation analysis showed TGase could improve melting temperature and texture by facilitating cross-linking. Covalent interaction based on ε-(γ-glutamyl)-lysine induced by TGase could play the main role in these improvements. This study suggested that TGase could be applied to design gelatin-based food for tailored quality properties through enzymatic cross-linking.     

牦牛绒过氧化氢/过硫酸铵脱色体系工艺优化及其机制

针对现有商业化牦牛绒脱色过程复杂、脱色时间长等问题,提出新型过氧化氢/过硫酸铵体系牦牛绒脱色工艺。在尽可能提高纤维白度的前提下尽量减少纤维损伤,通过单因素试验确定了脱色时间、过硫酸铵用量和试剂pH值,对脱色工艺进行探讨并与商业化脱色牦牛绒进行比较。结果表明:采用过硫酸铵质量浓度为400 g/L,试剂pH值为9,在室温下脱色为180 min可达到商业脱色牦牛绒的效果,脱色时间节省至原来的1/8;脱色机制分析发现,脱色过程中硫酸根自由基起主要作用,羟基自由基起次要作用。该脱色工艺简单,为牦牛绒高值化利用提供了新的解决方案。     

Inactivation efficacy of plasma-activated water: influence of plasma treatment time,exposure time and bacterial species

This study aimed to evaluate the influence of plasma treatment time, bacterial exposure time to PAW and bacterial species on the inactivation efficacy of plasma-activated water (PAW), with additional investigation of the inactivation mechanisms of PAW. Six bacterial species, including Listeria innocua, Staphyloccus aureus, Escherichia coli, Pseudomonas fluorescens, Shewanella putrefaciens and Aeromonas hydrophila were selected as the representative bacteria. The initial bacterial concentration was around 7 log CFU ml⁻¹ after mixing with PAW, and the inactivation efficacy was measured after different exposure times during the 4 °C storage. Scanning electron microscopy (SEM) images of the bacteria after PAW treatment were carried out to inspect the cell structure damage, and physicochemical properties of PAW, including pH, conductivity and long-living reactive species of H₂O₂, , and , were examined. The results showed that the inactivation efficacy of PAW was positively correlated with plasma treatment time and bacterial exposure time, and for the species examined in this study, the Gram-negative species were more sensitive to PAW than the Gram-positive species. Cell structure damage, including shrinkage, distortion, or holes, was observed after PAW treatment. The pH of PAW was acidified to 2.5–2.9, and conductivity was significantly increased to 518.0 μs cm⁻¹. and H₂O₂ were reduced during the 48 h storage, while an increased concentration was observed for . This study demonstrated that the processing parameters of plasma treatment time, exposure time and characteristics of bacteria can significantly affect the inactivation efficacy of PAW.     

2-Hydroxy-4-methoxybenzaldehyde inhibits the growth of Aspergillus flavus via damaging cell wall,cell membrane,manipulating respiration thus creating a promising antifungal effect on corn kernels

This study investigated the antifungal activity and the potential antifungal mechanisms of 2-hydroxy-4-methoxybenzaldehyde (HMB) against Aspergillus flavus (A. flavus). The minimum inhibitory concentration (MIC) of HMB in preventing spore germination was 70 μg mL⁻¹. HMB at MIC disrupted cell wall integrity by reducing the number of septa by 86.66% (P < 0.05) in mycelia and increased cell membrane permeability by about 14-fold (P < 0.05) evidenced by propidium iodide (PI) staining. Furthermore, HMB at MIC inhibited respiration by 33.33%. These results revealed that the antifungal activity of HMB against A. flavus could be attributed to the damaged cell wall integrity, cell membrane permeability and respiration metabolism. What’s more, A. flavus was completely restrained in corn kernels due to HMB. Therefore, HMB could be applied as an effective antifungal agent.     

Formation mechanism of porous reaction-bonded silicon nitride with interconnected pores in the presence of MgO

In porous reaction bonded silicon nitride, whiskers normally grow in globular clusters as the dominant morphology and deteriorate the pore interconnectivity. However, the ceramic microstructure was significantly transformed with the addition of MgO; specifically, the morphology was modified to a combination of matte and hexagonal grains. Microstructural observation along with thermodynamic studies suggest that MgO interfered with the presence and nitridation of SiO_(g). Consequently, rather than being involved in the whiskers’ formation, surface silica instead reacted with volatile MgO to form intermediate products. Through these reactions, whisker formation was blocked, and a porous interconnected structure formed which was confirmed by 3D tomography. After heat-treatment at 1700 °C, β-Si₃N₄ crystallized in a glassy matrix containing magnesium. Resulting samples had an open-pore structure with porosity of 74–84 vol. %, and density of 0.48-0.75 g.cm^?3. Combination of high porosity and pore size of <40 μm led to compressive strengths of 1.1–1.6 MPa.     

四川盆地震旦系灯影组丘滩体发育分布及对储层的控制

四川盆地震旦系灯影组储层主要发育于微生物丘滩体中，但不同成因类型丘滩体对储层的影响尚不明确。通过钻井岩心和野外露头观测、岩石薄片分析和物性测试等手段，将丘滩体划分为丘基、丘核、丘翼和丘坪4种微相，并根据微相的组合划分出台缘并进型丘滩体、台缘追补型丘滩体和台内饥饿型丘滩体3种丘滩体类型。台缘并进型丘滩体的生长速率快，与可容空间的增加速率相同步，其微相组合以"丘基+丘核"垂向加积为主，在海平面升降过程中易暴露于大气淡水环境，造成海水胶结作用弱、淡水溶蚀作用强，形成以格架溶蚀孔洞为主的储集空间，储层物性好，储集性能最优。台缘追补型丘滩体的生长速率次之，其早期的生长速率滞后于可容空间增长速率但后期逐渐同步，呈现出"丘基+丘核+丘翼/丘坪"侧向加积的微相组合；由于暴露于大气淡水环境的几率减小，其海水胶结作用强，淡水溶蚀作用减弱，储集性能稍差。台内饥饿型丘滩体的生长速率最慢，严重滞后于可容空间的增长速率，呈"云坪（丘基）+丘核+丘坪"微相组合，难以暴露于大气淡水环境，淡水溶蚀作用最弱，储集性能也最差。台缘带古地貌对丘滩体的生长速率影响较大，可控制丘滩体的沉积样式。陡坡台缘带有利于台缘并进型丘滩体发育，缓坡台缘带主要发育台缘追补型丘滩体，台内高地中发育台内饥饿型丘滩体。胡家坝-阆中-安岳地区一带的震旦系灯影组四段发育于典型的陡坡台缘带，是储层发育的最有利相带。     

多相流管输体系中水合物沉积机理研究进展

国内外对多相流管输体系中水合物沉积的研究虽然很多，但水合物沉积机理仍有待进一步研究。本文根据水合物沉积实验开展条件的不同，将多相流管输体系分为气体主导体系、油基体系、部分分散体系、水主导体系，总结了各体系的水合物沉积的主要机理，并提出了未来的发展方向。管输体系中水合物沉积机理包括水润湿沉积表面、水合物颗粒聚并、水合物的管壁膜生长、水合物颗粒的管壁粘附和水合物的颗粒着床沉积等。大多数学者认为：水合物的管壁膜生长是气体主导体系水合物沉积的主要机理；油基体系水合物沉积的主要机理是水合物颗粒的着床沉积；而部分分散体系和水主导体系的水合物沉积机理尚无统一定论，需进一步研究。多相流管输体系中水合物沉积研究未来的发展方向如下。①搭建全透明的流动环路，观测水合物在管路内实际的形成过程及沉积过程，对水合物沉积机理进行深入研究。②量化研究油水分层、油包水(或水包油)乳状液、自由水层对水合物沉积、堵塞的影响。③对于气体主导体系，除环状流和分层流外，有必要对段塞流、气泡流等其他常见的流型下沉积机理进行研究，重点在于开发一个综合模型来描述水合物沉积过程。④对于水主导体系，水合物形成过程出现的油水破乳的具体机理应是未来水合物沉积过程进行定量研究的方向。⑤国内外对垂直管、弯管及管阀件处水合物沉积堵塞理论研究较少，未来应着重这方面。