A Ti3C2Tx-carbon black-acrylic epoxy coating for 304SS bipolar plates with enhanced corrosion resistant and conductivity

A conducting and anticorrosive coating is crucial for the application of metal bipolar plates (BP) in proton exchange membrane fuel cell (PEMFC). In this work, a Ti₃C₂T_x (T)-carbon black (C)-acrylic epoxy (AE) coating is prepared on 304 stainless steel (SS) with enhanced corrosion resistance and conductivity. The corrosion resistance of the T-C-AE coating is investigated in a 0.5 M H₂SO₄ solution as compared to the AE, T, and T-AE coatings. The T-C-AE coated 304SS exhibits the strongest corrosion resistance with the most positive corrosion potential and the lowest corrosion current density of 0.00673 μA cm^?2 in all the samples, while retaining intact and compact surface morphology with the lowest metal ion dissolution even after immersed for 720 h. The addition of Ti₃C₂T_x and carbon black into the AE matrix greatly decreases interfacial contact resistance (ICR), and the T-C-AE coating achieves a low ICR of 15.5 mΩ cm^?2 under 140 N cm^?2 compaction force. The excellent anticorrosion performance is mainly attributed to the physical barrier and the cathodic protection provided by the stacked Ti₃C₂T_x (MXene) nanosheets in the T-C-AE coating. This eco-friendly, conducting, and anticorrosive T-C-AE coating has a good application prospect on SS BP of PEMFC.     

超高分子量聚乙烯纤维增强中空蜂窝模压复合材料性能研究

为研制车船等壳体所用的轻质、高强复合板材,选用超高分子量聚乙烯(UHMWPE)短纤维纱,制备成单层经纬为120根/(10 cm)的平纹组织,采用多组经纱持续更替交织层的方法制成2L(1+0)型、4L(2+1)型、6L(3+2)型3种多层角联锁结构织物,采用扦插芯棒、模压成型方法制成菱形蜂窝状的热固性环氧树脂基中空板,并与2块真空吸液法制成的面板组成“三合一”复合板,同时测定了复合板材的结构特征及其平拉、平压和弯曲性能。结果表明:3种类型复合板的密度均远小于水的密度,其中6L(3+2)型最小,为0.48 g/cm³;复合板层数越多,环氧树脂越难渗透尤其是在中空板菱形交叉点处,复合板平拉、平压、抗弯曲强度则呈现递增,制成的6L(3+2)型复合板试样平压强度可达到1.03 MPa。     

杂化包覆玄武岩鳞片/环氧涂料制备与性能

本文在环氧涂料中添加玄武岩鳞片，提高其防腐蚀性能。针对玄武岩鳞片的团聚问题，通过机械力化学改性工艺，采用正硅酸四乙酯、HY-311型钛酸酯偶联剂、E-44型环氧树脂对玄武岩鳞片进行杂化包覆，结果表明，杂化包覆后玄武岩鳞片的沉降时间从2h提高至96 h。杂化包覆玄武岩鳞片添加量为20%涂层的性能最优，附着力为13.40 MPa，耐盐雾时间为2000 h，在3.5%NaCl溶液中浸泡2000 h后，0.01 Hz的阻抗模值仍然有5.15×109 Ω·cm2。     

Synthesis of a novel DOPO‐based polyphosphoramide with high char yield and its application in flame‐retardant epoxy resins

A novel and highly effective flame retardant (FR), DOPO‐TPMP oligomer, was synthesized by a simple condensation of 4‐(hydroxymethyl)‐2,6,7‐trioxa‐1‐phosphabicyclo[2.2.2]octane‐1‐oxide and phosphorus oxychloride followed by a polycondensation reaction with 6‐(2,5‐dihydroxyphenyl)‐6H‐dibenzo[c,e][1,2]oxaphosphinine‐6‐oxide. The chemical structure of DOPO‐TPMP was well characterized using Fourier transform infrared and NMR spectra. DOPO‐TPMP was used as an additive‐type FR for epoxy resin (EP). The FR properties of the resultant EP composites were investigated by limiting oxygen index (LOI) test, UL‐94 vertical burning test and cone calorimeter measurements. Specifically, the EP composite containing 10.0% DOPO‐TPMP achieved a LOI value of 36.1%, V‐0 rating in the UL‐94 test and a 58% reduction in peak heat release rate. Further mechanism analysis attributed the enhanced flame retardancy to the increased char yield on the addition of DOPO‐TPMP. © 2019 Society of Chemical Industry     

汽车同步器齿环用耐高温结构胶膜的性能研究

同步器齿环与碳纤维耐摩擦材料是通过胶粘剂实现粘接,而胶粘剂耐高温性能的优劣则是决定其使用寿命的决定性因素。本文研究了环氧树脂E-51体系、环氧树脂AG80体系以及基材表面处理工艺对于结构胶膜耐高温性能的影响,采用熔融共混法制备了胶粘剂并以玻璃纤维布为背衬制备了耐高温结构胶膜。采用高低温拉力机对不同体系制备的结构胶膜进行了常温、200℃高温的钢材搭接剪切强度的测试。结果表明,对于E-51体系,提高体系交联密度可显著增大常温剪切强度,但高温剪切强度明显下降;对于四官能度的AG80体系,AG80的用量是影响其高温性能的主要因素,同时基材表面喷砂水洗处理后可显著增大结构胶膜与基材粘接有效面积,进而显著改善高温性能。所制备的结构胶膜较常用胶粘剂使用更加便捷,耐高温性能优良,满足同步器齿环使用要求。     

The combustion behavior of epoxy-based multifunctional electrolytes

Multifunctional or structural electrolytes are characterized by ionic conductivity high enough to be used in the electrochemical devices and mechanical performance suitable for the structural applications. Preliminary insights are provided into the combustion behavior of structural bi-continuous electrolytes based on bisphenol A diglycidyl ether (DGEBA), synthesized using the techniques of reaction induced phase separation and emulsion templating. The effect of the composition of the structural electrolytes and external heat flux on the behavior of the formulations were studied using a cone calorimeter with gases formed during testing analyzed using FTIR. The composition of the formulations investigated was changed by varying the type and amount of the ion conductive part of the bi-continuous electrolyte. Two ionic liquids, 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide (EMIM-TFSI) and 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM-BF₄), as well as a deep eutectic solvent (DES) based on ethylene glycol and choline chloride, were used. The results obtained confirm that time to ignition, heat release rate (HRR), total mass loss, as well as the composition of the gases released during tests depend on the composition of the formulations. Addition of liquid electrolyte is found to reduce the time to ignition by up to 10% and the burning time by between 28% and 60% with the added benefit of reducing the HRR by at least 34%. Gaseous products such as CO₂, CO, H₂O, CH₄, C₂H₂, N₂O, NO, and HCN were detected for all formulations with the gases SO₂, NH₃, HCl, C₂H₄, and NH₃ found to be for certain formulations only.     

Evaluation of different modelling conditions in the cohesive zone analysis of single-lap bonded joints

Cohesive Zone Models (CZM) are widely used for the strength prediction of adhesive joints. Different simulation conditions, such as damage initiation and growth criteria, are available for use in CZM analyses to provide the mixed-mode behaviour. Thus, it is highly relevant to understand in detail their influence on the simulations’ outcome. This work studies the influence of different conditions used in CZM simulations to model a thin adhesive layer in single-lap joints (SLJ) under a tensile loading, for an estimation of their influence on the strength prediction under diverse geometrical and material conditions. Validation with experimental data is considered. Adhesives ranging from brittle to highly ductile and overlap lengths (L_O) between 12.5 and 50 mm were considered. Different studies were considered: Variation of the elastic stiffness of the cohesive laws, different mesh refinements, study of the element type, and evaluation of several damage initiation and growth criteria. The analysis carried out in this work confirmed the known suitability of CZM for static strength prediction of bonded joints and pointed out the best set of numerical conditions for this purpose. Inaccurate results can be obtained if the choice of the modelling conditions is not the most suitable for the problem.     

环氧树脂基双组分水性聚氨酯的制备及其在木器涂料中的应用

为提高双组分水性聚氨酯的室温交联速度，将 N-苄基乙醇胺引入到环氧树脂制备了环氧树脂基水性多元醇，表征了多元醇的化学结构，并测定了其相对分子质量、粒径分布和玻璃化温度等主要技术参数。将环氧树脂基水性多元醇与多异氰酸酯配合制备了双组分水性聚氨酯，采用红外光谱法研究了室温交联反应过程。研究结果表明：多元醇分子结构中引入苄胺基加快了双组分水性聚氨酯的交联反应速度。将双组分水性聚氨酯制备成水性木器涂料，漆膜具有优异的耐冲击性、附着力、柔韧性、光泽、耐液体介质、硬度、丰满度等性能。     

新型活化环氧富锌涂层的耐腐蚀性研究

富锌涂料在防腐蚀领域具有广泛应用，然而其长效防护性能却受到锌粉活性影响。本文以冷涂锌涂层、传统环氧富锌涂层作为对照，研究了新型具有电化学活性的环氧富锌涂层在盐雾加速腐蚀试验后的耐腐蚀性。宏观形貌分析表明：盐雾加速腐蚀 1 800 h后，活化环氧富锌涂层表面并未出现锈点；采用扫描电子显微镜、维体式显微镜观察试验后涂层的表面形貌和涂层结构，发现活化环氧富锌涂层微观表面更加平滑，锌粉并未出现大面积的氧化，涂层内部大小锌粉颗粒均匀排列；通过电化学方法研究涂层的耐蚀机理与防护性，发现活化富锌涂层具有更持久的低防护电位。以上研究结果表明，较冷涂锌及传统环氧富锌涂层而言，新型活化环氧富锌涂层具有优异的长期防护性能，是值得关注和研究的一种新型技术。     

Morphology,thermal and mechanical performance of epoxy/polysulfone composites improved by curing with two different aromatic diamines

Epoxy/polysufone (PSF) composites cured with 4,4'-diaminodiphenyl sulfone (DDS) and 4,4'-diaminodiphenyl methane (DDM) were fabricated, and the effect of dual curing reaction of diamines with epoxy on morphology, mechanical, and thermal performance was investigated. DSC results indicated that DDM was more reactive than DDS and the activation energy decreased with the rising of DDM content. Structures with small domain size at the early stage of phase separation were fixed by the fast epoxy-DDM reaction. When the DDM content was elevated to a high level, large dual structures were changed to fine bicontinuous structures, which was favorable to improve the mechanical property. The mechanical performance of epoxy composites was enhanced and the maximum values were achieved when the DDM/DDS ratio was located at 75/25 (PSF/DDS0.25-DDM0.75). The flexural and tensile strength relative to epoxy/DDM system were enhanced more than those relative to epoxy/DDS, while the increase in toughness was the opposite. TGA measurement showed that thermal stability of epoxy/PSF composites was improved because of the restricting effect of continuous PSF domains on thermal motion of epoxy. DMA analysis exhibited two relaxation peaks for PSF/DDS0.25-DDM0.75, which could be attributed to the formation of phase separated morphology and epoxy network with different cross-link density.