正六棱台上下复合式礼盒成型结构设计

目的为了促进农特产品销售,设计一种正六棱台上下复合式轻便纸质礼盒。方法以传统竹木六棱食盒的盒型结构为设计原型,采用"T-X-T"三维成型方式进行盒型结构设计,通过提手设计和粘贴锁合结构来提高礼盒的便携性。利用SolidWorks软件对盒型结构进行力学模拟分析。结果利用"T-X-T"模式分解主体盒型结构,可以得到准确边缘关系结构图。侧板粘贴成盒过程中,通过增加粘合面积,可以提高盒型抗压强度。在相同纸张用料的情况下,侧板成角的角度对盒型的外尺寸有重要影响。侧板成角的角度设计范围在60°~90°之间;分析得出立体成型后外尺寸计算公式。结论所设计轻便纸盒为正六棱台上下复合式,美观大方。提手设计便携可折叠,反插式锁孔设计提高了盒盖的锁合能力。侧板采用粘贴成盒,提高了盒型抗压强度及堆码性能。     

多因素影响下苯乙烯-丁二烯-苯乙烯嵌段共聚物改性沥青性能分析

通过掺加不同含量糠醛抽出油、红油增塑剂与苯乙烯-丁二烯-苯乙烯嵌段共聚物(SBS)改性剂,分析其对SBS改性沥青各性能指标的影响,判断影响SBS改性沥青性能的主要因素。结果表明:改性沥青中SBS改性剂含量是提高软化点、弹性恢复的主要因素;糠醛抽出油含量增大则可明显提高其延度指标,且改善SBS改性沥青的离析程度;红油增塑剂含量增大可大幅提高SBS改性沥青的延度指标,但高温性能下降且离析严重,短期老化后指标下降幅度高于同等含量抽出油老化后指标。因此可在SBS含量确定的情况下,通过掺加适当的糠醛抽出油以改善SBS改性沥青的性能。     

Graphene oxide conversion into controllably carboxylated graphene layers via photoreduction process in the inert atmosphere

Abstract

The one-step method for graphene oxide (GO) simultaneous reduction and carboxylation via ultraviolet irradiation in the inert atmosphere has been reported. X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) data revealed that the proposed approach allows to obtain reduced graphene oxide (rGO) films, containing up to 10 at.% of carboxyl groups. The carboxyl groups concentration can be tuned within the range of 3 to 10 at.% by controlling the oxidation degree of the irradiated GO via the preliminary low-temperature air heating. Furthermore, no carboxylation effect is observed in the case of irradiation of the completely reduced GO films. This coincides with our previous results, validating the proposed model of GO carboxylation based on photoinduced conversion of basal-plane hydroxyl groups and ketones into carboxyl ones. Despite a different degree of carboxylation, all the obtained samples demonstrate almost complete elimination of basal plane groups and restoration of the graphene flakes aromatic structure. This fact is emphasized by the sheet resistance measurements, demonstrating that the obtained C-xy graphene exhibits high electrical conductivity. As a net result, the material obtained by the presented method shows promising applications in the manufacturing of biosensor transducers owing to both its conductive nature and presence of carboxyl groups, playing the role of the anchoring points for biomolecules.     

A comprehensive study on the size-dependent hygrothermal analysis of exponentially graded microplates on elastic foundations

Abstract

In this paper, the effects of hygrothermal conditions on various behaviors, such as bending, free vibration, mechanical and thermal buckling, of exponentially graded microplates lying on two-parameter elastic foundations are investigated. The trigonometric four-variable plate theory incorporated to the modified couple stress theory (MCST) is employed to derive the equations of motion. The present MCST contains an internal material length scale parameter, thus it can capture the size effect. The microplate is assumed to be subjected to a temperature rise and moisture concentration which are varied linearly through the thickness of the plate. Based on an exponential law, the material properties of the microplate are graded only in z direction. The equations of motion are solved analytically to obtain the displacements, stresses, eigenfrequencies and critical buckling load and temperature of the microplates. The present results are validated by comparing them with those previously published. The numerical examples reveal that considering the size effect and/or the elastic foundations leads to an increment in plate stiffness and thereby leads to a decrement in the deflection and an increment in eigenfrequency and buckling loads. It is also shown that the size effect is negligible for the thicker plate.     

Effect of Newtonian heating/cooling on free convection in an annular permeable region in the presence of heat source/sink

The influence of Newtonian heating/cooling in the presence of heat source/sink has been investigated on laminar free convective flow in a vertical annular permeable region. The mathematical model for the problem has been considered as a boundary value problem consisting of two simultaneous ordinary differential equations. The boundary value problem has been transformed to nondimensional form. This has given rise to a number of parameters representing both geometrical and physical features of the problem. Closed‐form analytical solutions of the governing equations have been obtained for two different cases of internal heat generation/absorption. To assess the effects of governing parameters on the fluid velocity and temperature, a number of profiles of these field variables have been presented. The efficacy of the distinct processes on the field variables has been discussed extensively. The main outcome obtained in this study is that the velocity as well as temperature is enhanced in the case of the Newtonian heating while the opposite behavior occurs in the Newtonian cooling for both cases of source and sink. Furthermore, the influence of the governing parameters has been shown on the skin friction, volume flow rate, and the Nusselt number.     

Development of starch-based peelable coating for edible packaging

This research characterised properties and stability of starch-based peelable coating film layers via mould dipping. Different ratios between rice starch (RS) and hydroxypropyl cassava starch (HS) containing agar blends were characterised for fluid rheology and properties of solid films. Layer-by-layer mould dipping in starch blend suspensions produced peelable shells. Rheology indicated that formability of thin-film layer on solid surface subsequently affected integrity of the shells. HS highly adsorbed water which plasticised matrices giving lower relaxation temperature (~10 °C) than RS and caused shrivelling and non-stable shell structures. RS increased crystallinity and non-homogeneity of films and reduced network flexibility and light transmission. IR spectra indicated modified hydrophobicity and hydrogen bonding of starch blends which governed water and oxygen permeability. Higher RS ratios significantly increased crystallinity which affected physical, mechanical and barrier properties during storage for three months. Findings indicated that HS provided flexibility and stability while RS improved formability of peeled shells.     

PBAT‒PLA膜袋受控需氧堆肥条件下的降解研究

目的 通过对广泛使用的PBAT–PLA生物降解膜袋在受控需氧堆肥条件下的降解机制研究，为生物降解塑料的大规模推广提供重要理论基础。方法 根据GB/T 19277.1—2011，在(58±2)℃需氧条件下，对PBAT–PLA膜袋进行为期160 d的生物降解测试(即工业堆肥)，并以常见的可降解材料微晶纤维素作为参比样品。对降解前后的材料进行红外、扫描电镜、能谱分析，并结合其所在堆肥样本的脂肪酶活性，从多角度探寻降解机制。结果 PBAT–PLA膜袋与微晶纤维素所在的堆肥脂肪酶活性都达到空白堆肥的3倍以上。红外显示由微晶纤维素水分子吸附、糖环打开、基团氧化形成的吸收峰加强，PBAT–PLA膜袋中的酯键峰明显减弱;扫描电镜发现降解的PBAT–PLA膜袋表面覆盖了微生物膜;能谱分析发现，碳元素大幅减少，氧元素增加。结论 微生物在PBAT–PLA膜袋表面生长形成生物膜，分泌大量脂肪酶，水解PBAT–PLA的酯键，使聚合物降解为不同链长的中间体或小分子，同时伴随着氧化，随后被作为碳源，在相关微生物体内被代谢利用，形成最终产物。     

Analysis and proposition of limiting current density measurement protocol

Limiting current density at different temperatures, backpressures, and balance gases can be used to separate molecular diffusion resistance, Knudsen diffusion resistance and local transport resistance of membrane electrode assembly (MEA). However, the measurement of limiting current density has no unified protocol. The diverse choices in the literature, either in the control of current or voltage or in the atmosphere like relative humidity and O₂ concentrations, make it difficult to compare the results and identify the true bottleneck hindering the mass transport. In this work, the current-voltage curves obtained by current scanning/stepping and voltage scanning/stepping methods under dilute O₂ of different concentrations and a wide range of relative humidity were measured and analyzed systematically. It is found that the voltage stepping method is superior to the other three ways of control for the reliable determination of the limiting current density. Aided with simultaneous electrochemical impedance spectroscopy measurement, the limiting current density can be determined with pinpoint accuracy. When the limiting current density is just used to qualitatively evaluate different MEA, the voltage scanning method can be used instead for its high time efficiency. The selection of the atmosphere also plays an important role in suppressing the distortion from excessive water and reducing the spurious contribution from proton conduction resistance. It is found that O₂ concentrations at 0.5 vol% and relative humidity at 90% can give the best estimation of O₂ transport resistance in membrane electrode assembly.     

Effect of air addition to the air electrode on the stability and efficiency of carbon dioxide electrolysis by solid oxide cells

In this study, the effect of air addition to the air electrode on the long-term stability and efficiency of solid oxide cells for CO₂ electrolysis, with 23.8% CO as protective gas in the fuel electrode, has been investigated. The results show that without continuous purging of the air in the air electrode (Cell-1), the degradation rate was 8.37%/kh in the 1070 h electrolysis process, while with 5 L/min air supplied to the air electrode (Cell-2), the degradation rate was 24.41%/kh. Impedance analysis indicates that the degradation of Cell-1 was mainly because of the increase in O^2? exchange polarization impedance, while the degradation of Cell-2 was caused mainly by the variation of ohmic impedance. The microstructural characterization indicated a decrease in active Ni in the fuel electrode in both Cell-1 and Cell-2, but the degree of nickel loss depended on the test time. At the outlet of the Cell-2, the appearance of carbon further explains the faster degradation rate, although the carbon deposition was not directly caused by the introduction of air into the air electrode. Energy spectral analysis shows that the air electrode in Cell-1 generated Sr rich phases, which indicates that the absence of air in the air electrode in the electrolysis process indeed causes more serious microstructure damage. The energy conversion efficiency could exceed 86% if the energy consumed for heating the air is ignored. This work provides a scenario for the application of solid oxide cells for CO₂ electrolysis without air purging in the air electrode.