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端羟基

端羟基的相关文献在1989年到2022年内共计383篇,主要集中在化学工业、化学、农学(农艺学) 等领域,其中期刊论文75篇、会议论文3篇、专利文献126441篇;相关期刊44种,包括橡胶参考资料、合成橡胶工业、化工学报等; 相关会议3种,包括2005年全国高分子学术论文报告会、2001年全国高分子学术报告会、全国第八次工业表面活性剂技术经济与应用开发会议等;端羟基的相关文献由937位作者贡献,包括张立群、潘广勤、严勇等。

端羟基—发文量

期刊论文>

论文:75 占比:0.06%

会议论文>

论文:3 占比:0.00%

专利文献>

论文:126441 占比:99.94%

总计:126519篇

端羟基—发文趋势图

端羟基

-研究学者

  • 张立群
  • 潘广勤
  • 严勇
  • 岳冬梅
  • 张田林
  • 齐永新
  • 于晶
  • 王海军
  • 介素云
  • 俞建敏
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 于兆鹏; 赵朕; 魏绪玲; 张昊; 刘若凡; 龚光碧; 伍一波
    • 摘要: 使用5-叔丁基-1,3-二(2-氯代异丙基)苯/四氯化钛引发体系,通过可控活性正离子聚合反应制备了含双活性链末端的聚异丁烯,再使用1,3-丁二烯封端制备具有烯丙基氯末端结构的聚异丁烯,并结合四丁基氢氧化铵存在条件下水解的方法制备了双端羟基遥爪聚异丁烯,研究了封端时间对封端反应的影响,探讨了所得聚合物的热稳定性和低温性能。结果表明,在四丁基氢氧化铵存在条件下,由含氯链末端亲核取代方式制备所得聚合物的端羟基转化率高,反应时间短,原料便宜易得且制备工艺简便,所得产物的热稳定性及低温性能优良。
    • 摘要: 申请公布号CN111471186A介绍了一种高性能共聚液态氟橡胶的制备方法及应用.该液态氟橡胶由端羧基氟橡胶(A)和端羟基氟橡胶(B)共聚组成BAB型共聚物,其中A和B物质的量的比为1/2,A的相对分子质量为800~9000,B的相对分子质量为800~9000,共聚液态氟橡胶的相对分子质量为1600~18000.
    • 李济亮
    • 摘要: 由于高低温下都具有良好的物理机械性能,以端羟基聚醚(HTPE)粘合剂为基的复合火箭推进剂配方已经成为一个新的推进剂系列。另外,HTPE推进剂已设计用来满足钝感弹药(IM)要求,尤其是用于符合IM的“慢速烤燃”试验以及满足用于战术导弹的要求。尽管HTPE被描述为一种新型粘合剂,但实际上早在20世纪50年代中期聚醚粘合剂就已用于配方中。
    • 林跃华; 龙清平; 聂建华
    • 摘要: 用天然松香与二元醇、二元酸和甲苯二异氰酸酯(TDI)合成了不饱和聚氨酯树脂,再加入稀释剂苯乙烯配制成家具涂料.采用国标方法对家具涂料的柔软性、硬度、抗冲击性、固化收缩率、附着力等物理性能进行测试.结果表明,不同二元醇对合成UP/PU树脂家具涂料的性能影响较大,其中乙二醇型UP/PU 的聚酯家具涂料且具有优良的抗冲击性、硬度较高、附着力好、固化收缩率低等优越性能.%The PU/UP unsaturated polyester have been synthetized by rosin, diatomic alcohol, diprotic acid and toluene diisocyanate (TDI), and the furniture coatings have been confected by adding styrene diluting agent into the PU/UP unsaturated polyester.Such physical property as softness, hardness, impact resistance, curing shrinkage, adhesion was investigated by a series of performance test method.The results indicated that the type of diatomic alcohol has a obviously effect on the properties of the furniture coatings, and those synthetized by using ethanediol as reagent possess very excellent physical properties.
    • 王学川; 李洋; 王海军
    • 摘要: 以椰子油脂肪酸二乙醇酰胺(CDEA)和2,2-双(羟甲基)丙酸(DMPA)为原料,对甲苯磺酸(p-TSA)为催化剂,采用“一锅煮”法合成了1~3代端羟基超支化聚合物.通过单因素实验优化了合成条件:反应温度160°C,反应时间4h,催化剂用量为1%(以CDEA质量计).通过FT-IR和1H NMR对产物的结构进行了表征,并测定了其表面活性.结果证明,该系列超支化聚合物具有不同的表面活性,可以根据需要,通过超支化改性的方式改变表面活性剂的表面活性.
    • 王亚东; 魏昌志; 鲍欣豪
    • 摘要: 合成了带羟基的聚丙烯酸酯高分子流平剂,不同羟基含量流平剂与普通流平剂在粉末涂料中的对比实验显示,端羟基流平剂具有更优异的增亮效果和流平性能.
    • 燕丰
    • 摘要: 上海工程技术大学开发出一种室温硫化聚异戊二烯橡胶的制备方法。使异戊二烯与仲丁基锂反应后加入环氧丙烷,制得端羟基聚异戊二烯;使HDI与端羟基聚异戊二烯反应,制得末端含NCO的聚异戊二烯;使末端含NCO的聚异戊二烯与6甲基异胞嘧啶反应,制得末端含UPy单元的聚异戊二烯;使末端含UPy单元的聚异戊二烯先形成聚异戊二烯的线性超分子聚集体,
    • 朱青; 施元旭; 范冬梅; 于翠平; 孙志明; 王校常
    • 摘要: 采用一步法,通过控制 AB2单体和三羟甲基丙烷的摩尔量,利用 Michael 加成反应制备得到一种端羟基超支化聚(胺酯)[Hyperbranched poly(amine-ester),HPAE],在此基础上研究了 HPAE 对茶多酚(tea polyphenols, TPs)的吸附特性及其反应时间和不同 pH 对该吸附行为的影响.结果表明:在298 K 条件下,pH 7,m(TPs)∶m (HPAE)=14∶1时,吸附量随时间的增加而增大,吸附6 h 后达到平衡,其实验所得平衡吸附量 Qe(experiment, Exp)为279.69 mg/g.吸附动力学模拟结果显示其准一级动力学模型、准二级动力学模型和 Weber-Morris 颗粒内扩散模型的 R 2分别为0.6148,0.9977,0.7445.准二级动力学模型拟合计算所得平衡吸附量 Qe,2(calculation, Cal)为302.11 mg/g,与 Qe(Exp)更为接近,因此该吸附过程符合准二级动力学方程,并且可能是物理吸附为主. HPAE 对茶多酚的吸附量主要受介质 pH 影响.在298 K 条件下,m(TPs)∶m(HPAE)=5∶1时吸附量随 pH 升高而增加,当 pH=4时,平衡吸附量 Qe 为72.56 mg/g;当 pH=7时,平衡吸附量 Qe 为194.90 mg/g.利用 pH 对吸附的效应特性,可通过调节 pH 方法方便洗脱吸附茶多酚.结果也显示该吸附剂对茶多酚的吸附能力远远大于相同吸附条件下大孔树脂的吸附能力.%Summary Tea polyphenols (TPs),as one kind of effective components in tea,are composed of catechins, anthocyanins,flavonoids,etc.Catechins take up 70% 80% of TPs.The epigallocatechin gallate (EGCG) is the most abundant and important bioactivity among TPs.Various studies have demonstrated that EGCG possesses a higher efficient bioactivity compared with other components of tea polyphenols, especially in inhibiting carcinogenesis and preventing metastasis in established tumors.Therefore,it was studied widely to develop new methods or techniques to enhance the efficiency of extraction and purification of TPs (including EGCG). Now column chromatography is the main method in purification industry of TPs.However,this technique involves of organic solvents and complex operational processes,which leads to an environmental pollution and increases the additional costs virtually.The demand for an environment-friendly and cheaper technique in TPs industry is growing rapidly while more people become to pay attention to ambient bio-environment,so seeking for some new methods or new materials is of great significance.The hyperbranched poly (amine-ester)(HPAE) is a new sort of materials,having internal cellular structure and a large amount of hydroxyl terminals.HPAE has been widely used as surface modifiers,drug carriers and adsorbents for heavy metal ions on account of its high adsorption properties and complex ability.To date,there is no research on the adsorption of tea polyphenols by HPAE.The objective of this study is to investigate the characteristics of HPAE as a new environment-friendly and low-energy adsorbent for the adsorption of tea polyphenols from aqueous solutions. The adsorbent HPAE was prepared by one step method with 1-(bis(2-hydroxyethyl)amino) pentan-3-one(as a AB2 monomer) and 2-ethyl-2-(hydroxymethyl)-1,3-propanediol (as a core molecule) in our laboratory.The kinetic experiments of adsorption were done with 10 mL HPAE(1%,w/w)and 40 mL 98% TPs solution(3.5 g/L) under the condition of 298 K and pH 7.0.The TPs contents in supernatant were determined by HPLC methods. The experiments about effects of different pH values (from 4.0 to 8.0) on adsorption also were done with similar steps with 40 mL TPs solution (1.25 g/L).Finally,the comparison of the adsorption capacity was made among HPAE and 1 6 kinds of traditional macroporous resins under the same condition of 298 K,pH=7. The results indicated that the adsorption of tea polyphenols by HPAE increased with time and reached equilibrium time in six hours of contact.The experimental value of the equilibrium adsorption capacity Q e(Exp)was 279.69 mg/g.The R 2 values were 0.614 8,0.997 7 and 0.744 5 for the pseudo-first-order kinetic model,pseudo-second-order kinetic model and intraparticle diffusion kinetic model,respectively.The pseudo-second-order kinetic model due to its higher R 2 value and closest Q e,2(Cal),was considered to be the best choice to describe the adsorption behavior of tea polyphenols by HPAE,suggesting that the adsorption mechanism might be a physical adsorption process. The increase in pH from 4 to 8 resulted in the increase in the TPs adsorption capacity,indicating that pH had an obvious effect on the TPs adsorption capacity onto HPAE and adsorbed tea polyphenols could be desorbed by controlling pH value in acid medium.The maximum adsorption capacity of HPAE was 194.90 mg/g at the present experiment condition,and far greater than the adsorption capacity of macroporous resins studied widely in TPs industry,such as LSA-8,LSA-20, XDA-1,HPD600,NKA,AB-8,D3520,D4020,PVPP and PA,etc. In conclusion,the new adsorbent HPAE has excellent adsorption and desorption properties for tea polyphenols. Its adsorption capacity could achieve 1 94.90 mg/g,and adsorption of TPs could be desorbed easily by adjusting pH instead of using organic solvents.HPAE shows a great potential as an environment-friendly and high efficiency substitute materials for tea comprehensive processing.
    • 李裕琪; 刘志琴; 胡开放; 焦宏宇; 刘秀兰; 王齐华; 潘广勤; 王廷梅
    • 摘要: 采用活性正离子聚合与硼氢化氧化的方法合成了端羟基聚异丁烯液体橡胶(HPIB),通过傅里叶变换红外光谱及核磁共振氢谱对HPIB的微观结构进行表征,在波数为3340 cm-1处出现1个很强的羟基吸收峰,在化学位移为3.62处出现与羟基相邻的亚甲基特征质子峰,说明聚合物中存在端羟基.
    • 摘要: 端羟基聚环氧氯丙烷的合成工艺 该专利涉及一种端羟基聚环氧氯丙烷的合成工艺。该工艺以二苯亚砜离子化合物为引发剂,向其中加入无水有机溶剂,常温下搅拌,使其完全溶解,
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