超声协助蒙脱土分散于聚磷酸铵阻燃聚丙烯的研究

阻燃剂能够增强聚丙烯（PP）的阻燃性能,但也会降低其力学性能,因此对阻燃剂进行改性以改善聚丙烯的力学性能显得至关重要。以传统的膨胀型阻燃剂（IFR）[由聚磷酸铵（APP）、季戊四醇（PER）、三聚氰胺（MA）组成]为PP阻燃。在合成APP过程中引入有机蒙脱土（OMt）。APP围绕OMt形成,剥离OMt使其能够较好地分散在阻燃剂中。为使OMt更好地分散在阻燃剂中,在磷酸氢二铵（DAP）、尿素（UREA）溶液中加入OMt,之后对溶液进行超声处理,蒸干后形成DAP-UREA-OMt与五氧化二磷反应生成APP。在PP中添加改性阻燃剂,有助于PP材料阻燃性能的提升与减缓力学性能的下降。当阻燃剂添加量为30%（阻燃剂添加量占总质量的质量分数）时,PP/IFR_APP/OMt复合材料的氧指数达到29.8%,通过V-0测试,拉伸强度为22.0 MPa,高出传统方法0.7 MPa。     

Application of ultrasound treatment for modulating the structural,functional and rheological properties of black bean protein isolates

The modulating effect of ultrasound treatments at varying powers and times on the structural and functional properties of black bean protein isolate (BBPI) was investigated. Compared with native BBPI, low-power (150 W) and medium-power (300 W) ultrasound treatments increased the solubility, foaming and emulsifying properties of BBPI, especially at 300 W, 24 min. This effect arises predominantly due to increased exposure of hydrophobic groups, which serve to increase the interactions between the protein and water molecules. Additionally, an increase in the protein surface activity improved the absorption of protein molecules at the oil–water and air–water interfaces. Rheology data showed that increased hydrophobic and hydrogen-bonding interactions improved the water-holding capacity of BBPI gels following ultrasound treatment. However, high-power (450 W) ultrasound treatment weakened the functional properties of BBPI, and this was likely due to the formation of macromolecular BBPI aggregates. Overall, this study indicates that ultrasound treatment could be a promising approach for modulating other plant protein resources as well as expanding the application of black bean protein.     

回火工艺对1Cr17Ni2不锈钢锻后回火硬度的影响

采用正交试验等研究了回火温度、回火时间、回火次数及冷却方式对1Cr17Ni2不锈钢锻后回火硬度的影响。结果表明,本试验中在回火温度630~730 ℃,回火时间120~360 min,回火1~3次以及冷却方式分别为空冷、堆冷、砂冷的条件下,对1Cr17Ni2钢锻后回火硬度影响因素的主次排序为:回火次数＞回火温度＞回火时间＞冷却方式,其中随着回火次数增加,硬度逐步下降,其余参数在试验参数范围内与硬度无明显正相关关系。在保温时间为240 min时,将回火温度升高至720 ℃,或在680 ℃下,将保温时间延长至720 min,进行一次回火,回火后空冷,硬度均高于3.5 HBS。在加热温度为680 ℃、回火时间为180~210 min,回火后空冷,回火3次可将硬度降低至3.6 HBS以下。     

时效工艺对纳米结构2297铝锂合金力学性能与微观组织的影响

采用535 ℃×2 h固溶制度,将热锻态2297铝锂合金固溶水淬后冷轧,冷轧压下量为95%,然后将轧制样品在不同温度(120~190 ℃)和时间(0~80 h)范围内进行时效处理。采用拉伸、扫描电镜(SEM)和透射电镜(TEM)等测试方法,分析时效温度和时间对铝锂合金组织与性能的影响。结果表明:时效前的大塑性变形能获得纳米结构组织,能促进T₁相均匀细小地析出,缩短合金达到峰时效的时间,最终成功制备了高强高塑性铝锂合金。在120~140 ℃温区内时效时,时效温度越高,达到峰时效的时间越短、强度越高。140 ℃达到峰时效时间缩短为40 h,此时合金的抗拉强度、屈服强度和伸长率分别为525 MPa、478 MPa和7.7%,主要强化相为细小的T₁相。在170~190 ℃温区内时效时,时效温度越高,达到峰时效的时间越短,但抗拉强度与屈服强度迅速下降。170 ℃时效8 h达到峰时效状态,此时合金的抗拉强度、屈服强度和伸长率分别是503 MPa、462 MPa和5.0%,主要强化相仍为T₁相,但已经明显粗化。     

刀刃角与岩石节理倾角对盘型滚刀破岩效率的影响

为了研究节理倾角与刀刃角对滚刀破岩效率的影响,运用ABAQUS有限元分析软件,采用Druker-Prager弹塑性本构模型模拟岩石材料,使用不同刀刃角的滚刀对不同节理倾角的岩石进行滚切加工,并结合破岩比能理论研究破岩效率,以破岩比能最小为依据确定不同节理倾角下的最优刀刃角。研究结果表明:不论倾角如何,节理层处的岩石破碎效果优于其他地方的破碎效果;在节理倾角为0°和30°时,滚刀的破岩比能呈波动的趋势,而且最优刀刃角为60°;在节理倾角为60°时,最优刀刃角为45°~50°;在节理倾角为90°时,最优刀刃角为40°~45°;随着节理倾角的增加,最优刀刃角呈不断减小趋势。该研究结果可为不同地质条件下盾构施工时的刀具选型提供一定的理论依据。     

某铜冶炼渣选矿厂SAB流程磨机衬板与钢球优化实践*

目前大多数铜冶炼渣选矿厂采用半自磨机—球磨机流程（SAB流程）进行粉磨作业，由于铜冶炼渣硬度大、性脆、易碎难磨，磨机衬板及磨矿介质消耗较大。针对某铜冶炼渣选矿厂开展了SAB流程衬板和钢球的优化研究。结果表明：①半自磨机用压条型铬钼钢衬板替代整体式锰钢衬板，使用寿命提高106.67%；球磨机用橡胶衬板替代锰钢衬板，使用寿命提高30%以上；检修强度大幅度降低，设备运转率明显提高。②半自磨机和球磨机由添加铸造钢球变更为锻造钢球，失圆率大幅降低；半自磨机补加球球径由120 mm调整为140 mm，增强了冲击破碎效果；球磨机补加钢球球径由60 mm调整为50 mm，磨矿浓度从75%提高到80%，研磨效果得到改善。③在磨矿细度保持不变的情况下，系统台时处理能力提高15.55%，钢球消耗降低26.32%，电力单耗降低26.67%，单位磨矿成本降低29.07%。企业经济效益和社会效益得到显著提高，对同行业具有一定的参考价值。     

热变形对GH4169合金中NbC析出相尺寸形貌影响研究

通过Gleeble3500热模拟试验机进行热压缩试验并结合微观组织观察和统计分析，研究了热变形对GH4169合金中NbC颗粒尺寸形貌、分布特征的影响规律。研究表明压缩过程中的绝热效应会导致试样心部温度的进一步升高，从而为变形过程中的NbC回溶提供条件。NbC颗粒与基体在变形过程中形成的高位错密度区促进了元素的扩散，并加速了小曲率半径的尖角区域回溶和钝化。随变形量的增加NbC回溶趋势增加，其平均尺寸与体积分数均呈降低趋势。变形过程金属流动会促进NbC颗粒的位移，在70%的变形量下，NbC颗粒平均间距增加趋势显著高于30%和50%变形量试样。因此随变形量的增加，NbC颗粒有从链状→链条弯曲→链条方向改变→弥散分布的分布特征，促进基体中原链状NbC呈细小、弥散分布。研究结果为GH4169闪光焊接性能的提高提供了直接的参考。     

Microstructure and Mechanical Properties of Cu Matrix Composites Reinforced byTiB2/TiN Ceramic Reinforcements

Cu matrix composites reinforced by TiB₂/TiN ceramic reinforcements (Cu/TBN composites) were prepared by hot pressing method. Prior to the hot pressing, Cu/TiB₂/TiN composite powders (CTBN powders), which were used as the starting materials of Cu/TBN composites, were fabricated by self-propagating high-temperature synthesis method. The CTBN particles were found to be in a special core-shell structure with a Cu-Ti alloy core and a TiB₂/TiN ceramic shell. The test results presented obvious improvements in mechanical properties. The highest ultimate tensile strength reached up to 297 MPa, 77 MPa higher than that of Cu. And the highest hardness reached up to 70.7 HRF, 15.7 HRF higher than that of Cu. A comparative study indicated that the core-shell structured particles could bring about more obvious strengthening effect than the traditional irregularly shaped particles, which was due to the improved Cu/ceramics interfacial bonding, the linkage strengthening effect of both TiB₂ and TiN, and higher load bearing ability of the core-shell structured reinforcements.     

微弧氧化Mg-3Al-1Zn镁合金应力腐蚀和腐蚀疲劳行为研究

本文主要对微弧氧化Mg-3Al-1Zn镁合金在空气和3.5 wt.%硫酸钠溶液两种环境下的应力腐蚀和腐蚀疲劳行为进行研究，并讨论其相互关系。微弧氧化处理后，Mg-3Al-1Zn镁合金的耐蚀性能得到明显改善。与Mg-3Al-1Zn镁合金基体相比，在空气中，微弧氧化后合金的应力腐蚀和腐蚀疲劳强度均下降了大约10 MPa。在3.5 wt.%硫酸钠溶液环境中，微弧氧化后合金的腐蚀疲劳性能仍然是恶化的，但是应力腐蚀强度却得到了显著改善，从58.24 MPa提高至202.08 MPa。这表明材料的力学性能（应力腐蚀和腐蚀疲劳）并不是与其腐蚀性能完全保持线性关系的。微弧氧化处理后镁合金在空气中的应力腐蚀断口为韧性断裂，在硫酸钠溶液环境中为解理断裂。而其腐蚀疲劳断口不论是在空气中还是在腐蚀环境中均为解理断裂。这主要是由于腐蚀环境和变换循环载荷的影响，两者共同作用将会加速裂纹扩展。这表明，周围环境和加载类型对材料断裂机理有重要影响。     

Fine-tuned,molecular-composite,organosilica membranes for highly efficient propylene/propane separation via suitable pore size

Fine-tuned, molecular-composite, organosilica membranes were fabricated via the co-condensation of organosilica precursors bis(triethoxysilyl)acetylene (BTESA) and bis(triethoxysilyl)benzene (BTESB). Fourier transform infrared and UV–vis spectra confirmed the co-condensation behaviors of BTESA and BTESB. The evolution of the network structure indicated that the incorporated BTESB decreased the membrane pore size, which was determined by a modified gas translation model according to the steric effect of the phenyl groups. The incorporation of BTESB to BTESA finely tuned the membrane structure and endowed the resultant composite membrane with improved separation properties. The BTESAB 9:1 membrane (molar ratio of BTESA/BTESB was 9:1) exhibited high C₃H₆ permeance at 4.5 × 10⁻⁸ mol m⁻² s⁻¹ Pa⁻¹ and a C₃H₆/C₃H₈ permeance ratio of 33 at 50°C. One of the most important developments of this study involved clearly defining the relationship between membrane pore size and C₃H₆/C₃H₈ separation performance for organosilica membranes in single and binary separation systems.