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21.
以双螺杆挤出机中的啮合块、螺杆元件作为研究对象,对其混合过程及混合性能进行研究,分析物料与添加剂的相互运动及变化过程。利用网格重叠技术和Ployflow软件对啮合块、螺杆元件的混合性能进行仿真,研究螺杆元件及不同转速下啮合块对应流体区域内的最大剪切应力,粒子在流体区域内的停留时间分布、分布指数、分离尺度等。结果表明:在啮合块流道内的混合过程中,啮合区域的两种粒子进行分布混合,其他区域的粒子在轴向运动到第2片啮合块时开始被带入啮合区,与另一种粒子进行分布混合;在相同转速下,啮合块的混合性能优于螺杆元件,随着转速的提高,啮合块的分散混合性能逐渐增强。 相似文献
22.
混凝土弹性模量是铁路梁场生产过程的重要控制指标,试验结果直接影响梁场生产进度与桥梁质量,而影响该项试验结果准确性的主要因素为试验设备智能化水平及操作过程信息化程度。通过本课题的研究,可提高弹模试验数据的准确性、及时性、完整性,减少弹模试验中试验人员数量,有效缩短弹模试验时间,实现弹性模量试验数据上传至工程管理平台,通过大数据对试验结果进行分析总结,为铁路领域梁体质量控制提供技术保障。 相似文献
23.
Natalia S Serkhacheva Nikolay I Prokopov Elena V Chernikova Elena Y Kozhunova Inna O Lebedeva Oleg V Borisov 《Polymer International》2019,68(7):1303-1314
Emulsifier‐free batch emulsion polymerization of n‐butyl acrylate and its semi‐batch copolymerization with 2,2,3,3,4,4,5,5‐octafluoropentyl acrylate and 2,2,3,4,4,4‐hexafluorobutyl acrylate both mediated by poly(acrylic acid) containing the trithiocarbonate group in the chain was employed to produce amphiphilic triblock copolymers. The polymerization‐induced self‐assembly of these copolymers in aqueous media gave rise to spherical core–shell particles. Irrespective of the experimental conditions, the polymeric product was characterized by a bimodal molecular weight distribution. The apparent violation of the reversible addition–fragmentation chain transfer polymerization mechanism may be attributed to restricted accessibility of the trithiocarbonate group in the self‐assembled block copolymers for propagating radicals that enter into the particle. Mean‐field theoretical arguments were employed to explain the exclusively spherical morphology of the particles observed in the experiment. © 2019 Society of Chemical Industry 相似文献
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R. Paxton Thedford Peter A. Beaucage Ethan M. Susca Corson A. Chao Katja C. Nowack Robert B. Van Dover Sol M. Gruner Ulrich Wiesner 《Advanced functional materials》2021,31(23):2100469
Mesoscale order can lead to emergent properties including phononic bandgaps or topologically protected states. Block copolymers offer a route to mesoscale periodic architectures, but their use as structure directing agents for metallic materials has not been fully realized. A versatile approach to mesostructured metals via bulk block copolymer self-assembly derived ceramic templates, is demonstrated. Molten indium is infiltrated into mesoporous, double gyroidal silicon nitride templates under high pressure to yield bulk, 3D periodic nanocomposites as free-standing monoliths which exhibit emergent quantum-scale phenomena. Vortices are artificially introduced when double gyroidal indium metal behaves as a type II superconductor, with evidence of strong pinning centers arrayed on the order of the double gyroid lattice size. Sample behavior is reproducible over months, showing high stability. High pressure infiltration of bulk block copolymer self-assembly based ceramic templates is an enabling tool for studying high-quality metals with previously inaccessible architectures, and paves the way for the emerging field of block-copolymer derived quantum metamaterials. 相似文献
27.
Synthesis and characterization of poly(ethylene oxide)‐based glycopolymers and their biocompatibility with osteoblast cells 下载免费PDF全文
Mummuluri Trinadh Kannan Govindaraj Tota Rajasekhar Marshal Dhayal Annadanam V Sesha Sainath 《Polymer International》2015,64(6):795-803
Poly(ethylene oxide)‐block‐poly(methacryl‐d ‐glucopyranoside) (PEO‐GP) and poly(methacryl‐d ‐glucopyranoside) (H‐GP) glycopolymers were synthesized by deacetylation of acetylated polymers which were synthesized via atom transfer radical polymerization. The synthesized glycopolymers were characterized using 1H NMR, 13C NMR and Fourier transform infrared (FTIR) spectroscopies, gel permeation chromatography (GPC), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The deacetylated polymers exhibited onset decomposition temperatures about 60 °C lower compared to the polymers having acetyl pendants. The glass transition temperature (Tg) of the acetylated homopolymer was 133 °C and that of the PEO‐based block copolymer was 124 °C. The deacetylated polymers H‐GP and PEO‐GP exhibited Tg values of about ?30 °C. Biocompatibility of the H‐GP and PEO‐GP glycopolymers was obtained by studying osteoblast cell adhesion, viability and proliferation in vitro. The cell viability showed an increase with increasing concentration of H‐GP from 0.1 to 1 µmol L?1 and then decreased with further increase in its concentration (10–1000 µmol L?1). PEO‐GP did not show a significant variation in cell viability on variation of its concentration from 0.1 to 1000 µmol L?1. The significant improvement in biocompatibility with osteoblast cells in the presence of PEO‐GP was considered as due to the covalently bonded PEO segment of the methacrylate glycopolymer block. © 2014 Society of Chemical Industry 相似文献
28.
Synthesis and characterization of copolymers with the same proportions of polystyrene and poly(ethylene oxide) compositions but different connection sequence by the efficient Williamson reaction 下载免费PDF全文
The AB type diblock PS‐b‐PEO and ABA type triblock PS‐b‐PEO‐b‐PS copolymers containing the same proportions of polystyrene (PS) and poly(ethylene oxide) (PEO) but different connection sequence were synthesized and investigated. Using the sequential living anionic polymerization and ring‐opening polymerization mechanisms, diblock PS‐b‐PEO copolymers with one hydroxyl group at the PEO end were obtained. Then, using the classic and efficient Williamson reaction (realized in a ‘click’ style), triblock PS‐b‐PEO‐b‐PS copolymers were achieved by a coupling reaction between hydroxyl groups at the PEO end of PS‐b‐PEO. The PS‐b‐PEO and PS‐b‐PEO‐b‐PS copolymers were well characterized by 1H NMR spectra and SEC measurements. The critical micelle concentration (CMC) and thermal behaviors were also investigated by steady‐state fluorescence spectra and DSC, respectively. The results showed that, because the PEO segment in triblock PS‐b‐PEO‐b‐PS was more restricted than that in diblock PS‐b‐PEO copolymer, the former PS‐b‐PEO‐b‐PS copolymer always gave higher CMC values and lower crystallization temperature (Tc), melting temperature (Tm) and degree of crystallinity (Xc) parameters. © 2015 Society of Chemical Industry 相似文献
29.
采用动态硫化法制备了苯乙烯-丁二烯-苯乙烯嵌段共聚物(SBS)增容高抗冲聚苯乙烯(HIPS)/高乙烯基聚丁二烯橡胶(HVPBR)热塑性硫化胶(TPV),考察了SBS用量对TPV物理机械性能的影响,表征了TPV的微观形貌,并研究了TPV的Mullins效应及其可逆性。结果表明,SBS可显著改善HIPS/HVPBR体系的相容性,其用量为12份时,TPV的物理机械性能较好;SBS增容TPV的断面平整、结构致密,界面相互作用明显增强;SBS增容TPV在循环单轴拉伸过程中出现明显的Mullins效应,提高应变速率时,TPV的最大应力和内耗呈增大趋势,瞬时残余形变则减小;当拉伸比相同时,TPV经第1次拉伸热处理后,第2次单轴拉伸中TPV的最大应力和内耗均增大,瞬时残余形变则减小。 相似文献
30.
In this work, the reversible addition-fragmentation chain transfer (RAFT) polymerization was utilized to synthesize the amphiphilic diblock copolymers of poly(methacrylic acid)-b-poly(2,2,2-trifluoroethyl methacrylate) (PMAA-b-PTFEMA) via one-pot two-step reaction protocol. The controlled radical polymerization of MAA monomer was first carried out in pure water by using 4-cyanopentanoic acid dithiobenzoate (CADB) as chain transfer agent. Subsequently, the as-synthesized PMAA homopolymers with dithiobenzoate end-groups were employed as macro-CTA and chain-extended in situ with the hydrophobic TFEMA monomer. The reactions were carried out in 1,4-dioxane/water medium. Both the polymerization of PMAA and PTFEMA blocks showed the well controllability on the molecular weighs and distributions. It was found that the amphiphilic diblock copolymers formed the stable spherical particles via the polymerization-induced self-assembly. Meanwhile, the effect of various parameters, such as the concentration ratio of TFEMA monomer over PMAA macro-CTA, the solvent condition (different ratio of 1,4-dixane/water), and the pH, on the RAFT polymerization of TFEMA monomer were investigated in detail. Their kinetic results suggested that the propagation of TFEMA monomer on the macro-CTA was performed at the particle/water interfaces. The concentration of chain transfer agents at the interfaces determined the polymerization rate. Finally, the stability of the fluorinated polymer dispersions was also evaluated in this work. 相似文献