聚碳酸酯水桶中5种酚类物质的残留量检测以及迁移风险评估

目的利用超高效液相色谱法研究聚碳酸酯水桶(polycarbonate, PC)中5种酚类物质(苯酚、双酚A、对叔丁基苯酚、对枯基苯酚和2,4-二叔丁基苯酚)的残留量并对迁移风险进行评估。方法利用溶解-沉淀法对30批PC水桶中的酚类物质进行提取。参考GB 31604.1-2016《食品安全国家标准食品接触材料及制品迁移试验通则》和GB 5009.156-2015《食品安全国家标准食品接触材料及制品迁移试验预处理方法通则》对PC水桶进行迁移试验。利用超高效液相色谱法对提取液和迁移试液中的酚类物质进行定性和定量分析。结果在线性范围0.02～5mg/L内,线性系数均大于0.999,加标回收率在82%～109%之间,相对标准偏差范围为0.6%～5.2%(n=3)。30批饮用水桶中,各酚类物质的检出率分别为73%、93%、50%、43%和93%。食品模拟物为水的迁移实验中,只有苯酚和双酚A有检出,且数值都小于国家标准中的限量值。结论 5种酚类物质在PC水桶中的迁移风险都较小,研究可为PC产品的质量控制和酚类物质风险监测提供技术基础。     

Yield stress distribution in injection‐moulded glassy polymers

A methodology for structural analysis simulations is presented that incorporates the distribution of mechanical properties along the geometrical dimensions of injection‐moulded amorphous polymer products. It is based on a previously developed modelling approach, where the thermomechanical history experienced during processing was used to determine the yield stress at the end of an injection‐moulding cycle. Comparison between experimental data and simulation results showed an excellent quantitative agreement, both for short‐term tensile tests as well as long‐term creep experiments over a range of strain rates, applied stresses, and testing temperatures. Changes in mould temperature and component wall thickness, which directly affect the cooling profiles and, hence, the mechanical properties, were well captured by the methodology presented. Furthermore, it turns out that the distribution of the yield stress along a tensile bar is one of the triggers for the onset of the (strong) localization generally observed in experiments. © 2015 Society of Chemical Industry     

Fully renewable limonene‐derived polycarbonate as a high‐performance alkyd resin

Limonene‐derived polycarbonate‐based alkyd resins (ARs) have been prepared by copolymerization of limonene dioxide with CO₂, catalysed by a β‐diiminate zinc–bis(trimethylsilyl)amido complex, and subsequent chemical modification with soybean oil fatty acids using triphenylethylphosphonium bromide as the catalyst. This quantitative partial modification was realized via epoxy–carboxylic acid chemistry, affording ARs with higher oil lengths, lower polydispersities and higher glass transition temperatures (T_g) in comparison to a conventional polyester AR based on phthalic acid, multifunctional polyol pentaerythritol and soybean fatty acid. The novel limonene polycarbonate AR and the conventional polyester AR were evaluated as coatings and both the physical drying (without the presence of the oxidative drying accelerator Borchi® Oxy Coat) and chemical curing (with Borchi® Oxy Coat) processes of these coatings were monitored by measuring the König hardness and complex modulus development with time. A better performance was obtained for the alkyd paint containing polycarbonates modified with fatty acids (FA‐PCs), which showed a faster chemical drying, a higher König hardness and a higher T_g in coating evaluation, demonstrating that the fully renewable FA‐PCs are promising resins for alkyd paint applications. © 2019 Society of Chemical Industry     

FDM用PETG系列耗材的改性研究

对市售聚对苯二甲酸乙二醇酯-1，4-环己烷二甲醇酯（PETG）丝材及原材料进行研究，选用PETG 2012作为制备熔融堆积成型技术（FDM）用PETG丝材的基体树脂。选用聚碳酸酯（PC）对基体PETG进行增韧增强改性，并制成3D打印高分子丝材进行打印测试，探讨了PC含量对PETG耗材及制件性能的影响。结果表明，在低PC含量下，PETG与PC的相容性较好，PETG与PC制件未出现明显的分层，分布比较均匀；共混物的流动性随着PC含量的增加而降低，且打印件的维卡软化温度和热变形温度随着PC用量的增加而增加；此外，PC材料的加入使得PETG打印件的力学性能得到较大改善：打印件的拉伸强度随着PC用量的增加而增大，缺口冲击强度却随着PC用量的增加呈现先增加后减小的趋势； PETG/PC的配比为1∶1时，可制得力学性能优异的3D打印耗材。     

Influence of aliphatic polycarbonate middle block on mechanical and microstructural behaviour of triblock copolymers based on poly(l‐lactide) and polycarbonate

Three different ABA‐type triblock copolymers each containing biodegradable aliphatic polycarbonate as the middle block and poly(l ‐lactide) as the outer blocks were synthesized and the influence of the methylene chain length of the aliphatic polycarbonate middle block on various properties of the triblock copolymers was evaluated. Differential scanning calorimetry and wide‐angle X‐ray diffraction studies revealed that the incorporation of the outer blocks reduced the crystallinity of the middle aliphatic polycarbonate block. Variation of methylene chain length of the middle block led to a change in morphology from spherical to cylindrical as evidenced from atomic force microscopy studies. In addition, the mechanical properties of the block copolymers showed semi‐ductile to quasi‐brittle behaviour depending upon the composition of the middle block which was also confirmed using scanning electron microscopy. Dynamic mechanical analysis of the triblock copolymers indicated that storage modulus increased with a decrease in methylene chain length. © 2018 Society of Chemical Industry     

聚碳酸酯型水性聚氨酯(下)

<正>(接上期)3.2.1以聚碳酸芳酯制备PCDL-WPU PCDL型PU在耐热及耐水解性方面是PU中最佳的耐久等级,作为耐久性膜、汽车和家具用人造皮革涂层材料(尤其是水性涂料)、胶粘剂等被广泛应用。但目前广泛市售的聚碳酸酯二醇,主要是由1,6-己二醇合成所得,其缺点:(1)因系结晶体,常温下为蜡状,无流动性,操作困难;(2)制得的PU软段的凝集性高,低温时的柔韧性、伸长率、弯曲度以及回弹性欠佳,限制其广泛应用;(3)所得PU溶液的黏度高,成型或涂敷时操作性差;(4)由其制得的人造皮革,其质感差,     

PC基光散射材料的制备研究

将丙烯酸、有机硅光扩散等助剂混合后,经过平行双螺杆挤出机制备了光扩散聚碳酸酯,研究不同配比的丙烯酸和有机硅光扩散剂对聚碳酸酯光学性能的影响。结果表明:采用不同含量的丙烯酸和有机硅光扩散剂复配,添加不同的量可得到不同光学性能的光扩散聚碳酸酯。     

KOH/γ–Al_2O_3催化合成聚(碳酸三甘醇)酯二醇

以碳酸二乙酯(DEC)和三甘醇(TEG)为原料,KOH/γ–Al2O3为催化剂,通过酯交换缩聚反应合成了成本低、性能优越的聚(碳酸三甘醇)酯二醇(PTEGCDL)。考察了反应条件对该过程的影响,得到了最优合成工艺条件。当催化剂的质量为TEG质量的0.5%时,先常压、150~160℃下反应3 h,然后减压180℃下反应5 h,可得目的产物PTEGCDL。对合成产物的结构进行了表征,并推测了可能的反应机理。     

PC微流控芯片黏接筋与溶剂的协同辅助键合

为了在微流控芯片上形成封闭的微通道等功能单元,克服热压键合中微流控结构的塌陷和热压所致芯片微翘曲对后续键合的影响,提出了一种适用于硬质聚合物微流控芯片的黏接筋与溶剂协同辅助的键合方法。以聚碳酸酯(PC)微流控芯片为研究对象,通过热压法在PC微流控芯片上的微通道两侧制作凸起的黏接筋,通过化学溶剂丙酮微溶PC圆片的表面,然后将PC圆片与带有黏接筋的PC微流控芯片贴合、加压、加热,从而实现微流控芯片的键合。分析了键合机理,并对键合工艺参数进行了优化。实验结果表明:键合质量受丙酮溶剂溶解PC圆片的时间和键合温度的影响,能够保证键合质量的最佳键合温度为80~90°,溶解时间为35~45s,芯片的键合总耗时为3min。与已有键合工艺相比,所提出的黏接筋与溶剂辅助键合工艺有效提高了键合效率。该键合方法不仅适用于具有不同宽度尺寸微通道的微流控芯片,还可扩展用于不同材料的硬质聚合物微流控芯片。