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合成了2-(4-邻苯二甲酰肼基)甲酰胺基苯甲酸,通过红外、核磁对化合物进行了表征。探索了该化合物的荧光、化学发光、紫外等发光性能。结果表明,该化合物是一种发光性能良好的化学发光试剂。 相似文献
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本文合成了以聚乙内酯为溶剂化链的超分散剂,考查了该分散剂对磁浆的分散作用。结果表明使用超分散剂能提高涂带后的磁性能,超分散剂以胺基和羧基共同作为锚固基团时分散效果较好,两种锚固基团的最佳配比与溶剂化链的分子量有关,“梳状”分子结构能提高超分散剂的分散效果。 相似文献
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对含取代氨端基的聚酯类超分散剂的合成方法进行了研究,并为获得适当长度的聚酯链选择了最佳合成条件;同时扼要论述了这类超分散剂的结构特性,以及对于有机颜料粒子表面的吸附作用、分散体系的稳定作用以及对涂料、油墨生产的重要意义。 相似文献
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SnC12作催化剂,1,6-已二醇和氯乙酸在环己烷中网流3h获得1,6-已二醇双氯乙酸酯,然后再与二乙胺在室温下反应3h,合成了新化合物二(N,N-二乙基甘氨酸)-1,6-已二醇酯,总产率达71.8%,并对影响1,6-已二醇双氯乙酸酯产率的因素进行了探讨。 相似文献
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合成了一种新型配体N,N′-双(2-氨乙基)邻苯二甲酰胺(L),并合成了它的Cu(Ⅱ)配合物。进行了核磁、元素分析、红外、荧光等表征实验。结果表明,配体可以与Cu(Ⅱ)形成配合物。 相似文献
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以N,N′-亚甲基双丙烯酰胺和乙醇胺,通过氮杂迈克尔加成聚合反应,合成了聚酰胺胺主链(PAA),然后通过侧链羟基与加入的ε-己内酯进行开环聚合反应,得到聚酰胺胺接枝聚己内酯梳状超分散剂(PAAPCL)。利用红外光谱、核磁氢谱和凝胶渗透色谱对PAAPCL进行了结构表征。将PAAPCL加入含有二氧化硅填料的光固化涂料中,制得光固化复合涂层。结果表明:随着PAAPCL添加量的增加,以及PAAPCL聚己内酯侧链聚合度的提高,光固化涂料在低剪切速率下的黏度下降,沉降稳定性提高。当PAAPCL添加量为二氧化硅质量的5%,PAAPCL侧链聚己内酯聚合度为15时,光固化涂料呈现出牛顿流体特征,并且在室温下静置28 d后仍保持较好的稳定性。添加了PAAPCL后的光固化涂膜的断裂伸长率和拉伸强度提高,透光率、光泽提升,磨耗由(16.3±0.5)mg下降至(12.0±0.3)mg。 相似文献
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Among the post‐reactor derivatives of poly‐(propylene) (PP), maleinated poly(propylene) (PPMAA) has become a success on the market because it is more polar than PP and, more importantly, because it is reactive. But PPMAA has a problem: it is prepared from PP by peroxy initiated MAA addition, a process in which the PP chains are seriously degraded. Therefore, PPMAA cannot compete mechanically with PP. In this report, a reactive extrusion process is discussed whereby degraded PPMAA chains are extended again by chain coupling through a diamine. This leads to branched clusters of PPMAA chains. Crosslinking occurs, too, but only on a local level. The extended products are impact resistant while the original PPMAA was brittle. 相似文献
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以端基为8个伯氨基的树枝状化合物〔PAE(NH2)8〕和聚氧乙烯〔PEO-A(454)〕或丙烯酸钠(SAA)与聚氧乙烯为原料合成了含聚氧乙烯链端树枝状聚(胺-酯)(PAE-PEO-A和PAE-SAA-PEO-A)。通过正交实验讨论了反应温度、反应时间及原料配比对产物产率的影响,并用FTIR、1HNMR、13CNMR及GPC对试样进行结构表征。测定了含聚氧乙烯链端树枝状聚(胺-酯)的表面张力及对苯甲酸、水杨酸的增溶性。实验结果表明,当反应温度为65℃,反应时间为96 h,原料的配比量n〔PAE(NH2)8〕∶n[(PEO-A(454)]=1∶16,以甲醇为溶剂,产物产率为88.30%。PAE-PEO-A溶液的临界胶束质量浓度为0.007 5 g/L,最小表面张力为43.8 mN/m。PAE-PEO-A对苯甲酸、水杨酸都有增溶性,且增溶能力随着它们的表面官能团数的增多和浓度的增加而增大。当反应温度为50℃,反应时间为96 h,原料的配比量n〔PAE(NH2)8〕∶n(SAA)∶n〔PEO-A(454)〕=1∶12∶8,以甲醇为溶剂,产物产率为48.83%。PAE-SAA-PEO-A水溶性极好,其表面张力与水接近,几乎不具有表面活性。PAE-SAA-PEO-A对苯甲酸和水杨酸有良好的增溶性,尤其是对水杨酸的增溶性明显。在相同质量浓度0.500 g/L时,PAE-SAAPEO-A对水杨酸的增溶量约为PEG-400的2.4倍。 相似文献
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Xun Li Min Xia Di Qiu Ren Long Zihan Huang Jie Li Shijun Long Xuefeng Li 《大分子材料与工程》2021,306(3):2000638
High-viscosity, low-crosslinked poly(butylene terephthalate) (PBT) from organic chain extenders and inorganic particles are prepared. PBT modification adopted from multifunctional, commercially available chain extension containing nine epoxy groups (ADR9) occurs in the first-step chain extension; hydroxyl addition modified dioxazoline (BOZ) serves as the second step. Anion stratiform inorganic hydrotalcite (HT) is used to adjust the crystallization behavior and damp-heat aging properties of PBT. The reaction between the chain extender and PBT end-groups such as carboxyl (–COOH) and hydroxyl (–OH) enhances the interfacial bonding between the PBT matrix and dispersed HT phases. With a fraction of chain extenders in the PBT matrix, the chain-extended PBT exhibits higher mechanical properties, intrinsic viscosity, average molecular weight, and melt viscosity than those of unmodified PBT. Damp-heat aging resistance measurements show correlation with initial carboxyl content in the resin. Reducing the concentration of carboxyl end-groups in the resin is shown to increase hydrolytic stability. The modified PBT resin can be used in optical fiber communication cable industry for its high level of damp-heat aging resistance as well as good mechanic properties. 相似文献
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采用均苯四甲酸酐(PMDA)作为聚对苯二甲酸乙二醇酯(PET)的扩链剂制备了扩链改性PET(CEPET),并以超临界二氧化碳(CO2)为物理发泡剂,采用釜压法制备了CEPET泡沫;通过旋转流变仪和扫描电子显微镜研究了CEPET的流变性能和CEPET泡沫的泡孔结构。结果表明,随着PMDA含量的增加,CEPET试样的储能模量逐渐增加,损耗因子逐渐降低,CEPET的熔体强度明显高于纯PET;CEPET泡沫的泡孔形态得到改善,发泡倍率得到提高;加入1.0 份(质量份,下同)扩链剂时,发泡倍率能够达到32.55倍。 相似文献
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用过氧化氢对聚马来酸酐进行氧化,制备出了一种聚过氧马来酸消毒剂。研究了氧化反应的条件、产物的稳定性和杀菌效果。结果表明,在n(酸酐基)∶n(H2O2)=1∶1.25,温度5℃的条件下反应6 h,可得到过氧羧基浓度为2.95 mol/L的消毒剂溶液。向此溶液中加入稳定剂乙二胺四甲叉膦酸(EDTMP)后,在20℃保存,60 d内过氧羧基的浓度基本不变,100 d后浓度只降低10%。过氧羧基浓度为0.012 5 mol/L和0.025 mol/L的聚过氧马来酸稀释液,可分别在10 m in和5 m in内完全杀灭金黄色葡萄球菌和大肠杆菌,并且对金属基本无腐蚀或只有轻度腐蚀。该消毒剂已经过扩大实验,杀菌性能良好。 相似文献
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Andreas Himmelsbach Tobias Standau Justus Kuhnigk Tobias Bubmann Yavuz Akdevelioglu Mohammadreza Nofar Holger Ruckdäschel 《大分子材料与工程》2023,308(7):2200683
Polyesters, such as poly (butylene terephthalate) (PBT), owe a rather low melt strength, which is considered as not beneficial for foaming. To overcome this issue, a typical attempt is the incorporation of chemical modifications—so-called chain extenders (CE)—in the reactive extrusion process. In this study, the reaction kinetic variables are investigated depending on the material and process parameters. For this purpose, different series of experiments are performed with varying PBT with different molecular weights and the commonly used CE, Joncryl ADR4468, on a micro compounder. The screw force is recorded and analyzed using an Avrami and an Arrhenius plot. First, the amount of CE is systematically varied. To study the course of the reaction in more detail, the reaction is stopped in a series of measurements (10, 30, 60, and 90 s after complete filling). Gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FT-IR), and Raman spectra are recorded. In the second series, the effect of processing temperatures between 250 and 270 °C is investigated, and finally, in the third series, the average molecular weight of PBT is varied. It could be shown that the activation energy seems to be dependent on the initial molecular weight; lower molecular weights result in lower activation energy. 相似文献
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总结了近年来国内外关于聚羟基丁酸酯(PHB)和聚羟基丁酸酯-co-羟基戊酸酯共聚物(PHBV)在增韧和增塑改性方面的研究进展。通过应力-应变行为和冲击强度等性能指标,对弹性体、酚类化合物、反应性增韧、超高相对分子质量聚乙二醇、淀粉、羟基烷酸酯、热处理等增韧改性方法和效果、改性产物进行了评述;通过熔点、玻璃化转变温度、冷结晶温度等性能指标,对共聚改性、中小相对分子质量聚乙二醇、环氧大豆油等增塑剂增塑改性方法、效果以及改性产物进行了详细介绍。最后对PHB和PHBV生物降解材料的发展前景进行了展望。 相似文献
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超支化聚酰胺酯对聚乳酸增韧改性的研究 总被引:5,自引:0,他引:5
采用熔融共混的方法,用生物可降解的超支化聚酰胺酯(HBP)对聚乳酸(PLA)进行增韧改性,制备出具有良好韧性的PLA复合材料。对不同HBP含量的共混物的红外光谱、热性能和力学性能进行了测试和分析。红外光谱显示PLA和HBP间存在氢键作用。HBP的加入使PLA的结晶度从30.99%降低到18.58%。当HBP含量增加到10%时,PLA共混物的拉伸强度略有提高,且断裂伸长达到43.06%。结果表明:HBP的加入对PLA起到了很好的增韧作用。 相似文献