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2-甲基吡啶

2-甲基吡啶的相关文献在1983年到2022年内共计164篇,主要集中在化学、化学工业、工业经济 等领域,其中期刊论文108篇、会议论文4篇、专利文献470408篇;相关期刊73种,包括商丘师范学院学报、科技信息、黑龙江医药等; 相关会议3种,包括第2届国际有机电化学与工业研讨会暨第12届全国有机电化学与工业学术会议、第十届全国有机电化学与工业学术会议、第十三次全国电化学会议等;2-甲基吡啶的相关文献由379位作者贡献,包括张恒彬、李克昌、曹学静等。

2-甲基吡啶—发文量

期刊论文>

论文:108 占比:0.02%

会议论文>

论文:4 占比:0.00%

专利文献>

论文:470408 占比:99.98%

总计:470520篇

2-甲基吡啶—发文趋势图

2-甲基吡啶

-研究学者

  • 张恒彬
  • 李克昌
  • 曹学静
  • 张玉敏
  • 秦必政
  • 刘善和
  • 葛九敢
  • 薛谊
  • 江镇海
  • 肖国民
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 张聪; 刘小琴
    • 摘要: 采用捏合法制备了以铬为主,银、铈为助剂的钒钛催化剂,并在固定床反应器中考察其催化2-甲基吡啶氨氧化合成2-氰基吡啶。结果表明,在反应温度374°C,物料n(2-甲基吡啶)∶n(氨)∶n(空气)=1∶2.5∶45和空速1.2 h^(-1)的最佳反应条件下,2-甲基吡啶转化率为99.6%,2-氰基吡啶收率为88.4%。
    • 钱前; 陈晨; 吴李瑞; 孙玉栋; 黄燕; 鲁宁宁
    • 摘要: 采用Re2O7负载ZSM-5沸石分子筛作为催化剂,以固定床为反应器,催化2-甲基吡啶合成2-乙烯基吡啶.系统地考查不同硅铝质量比的ZSM-5分子筛催化剂、反应温度、反应时间以及物料配比对2-乙烯基吡啶收率的影响,筛选出合适的反应条件.反应的最优条件为选取硅铝比为25的ZSM-5分子筛负载Re2O7,2-甲基吡啶∶甲醛为1∶4,反应温度为335°C,此时2-乙烯基吡啶的收率可达89.7%.该工艺操作简单,安全性高,条件温和,不易腐蚀管道,反应时间短,收率高,适合工业化生产.
    • 刘敏; 吴李瑞; 刘典典; 吴超; 黄燕
    • 摘要: 以Fe-Mn/ZSM-5分子筛为催化剂,固定床为反应器,采用吡啶与甲醇合成2-甲基吡啶.系统地考查了Fe含量、Mn含量、催化剂用量、原材料摩尔比、反应温度对2-甲基吡啶吸收率的影响,筛选出合适的反应条件.反应的最优条件为Fe含量1.2%,Mn含量0.8%,反应温度350°C,催化剂用量5%,吡啶∶甲醇=1∶1.3,此时2-甲基吡啶的收率达93%以上.该工艺操作简单,安全性高,收率高,适合工业化生产.
    • 温兰兰; 赵志华; 李宁; 徐道明; 刘典典
    • 摘要: 采用三乙胺作为催化剂,常压合成2-羟乙基吡啶,考查了催化剂种类、三乙胺用量、物料配比、温度、回流时间对反应收率的影响,得出优化的反应条件:三乙胺作为催化剂,摩尔量为0.06 mol时,2-甲基吡啶与多聚甲醛摩尔比为3:1时,阶段升温反应,110°C回流反应20 h,反应收率达到85.3%.
    • 程新炎; 王志远; 江梅珍; 王敏炜
    • 摘要: Three sorts of 2-methylpyridinium ionic liquids,which composed of five different kinds of cations and two kinds of anions,were synthesized via methods of one-or two-steps under existence of no solvent.The structures and acidities of these ionic liquids were characterized by FT-IR and UV-Vis spectroscopy.The association between the structure of ionic liquid and its acidity was investigated.The esterification reaction of capric acid and tripolyglycerol was used as the probe reaction,and the catalytic performance of these ionic liquids was examined.The results showed that:(a) When the cations are the same,the acidities of ILs meet the order HSO4->H2PO4-,which is in line with anionic acidity;while the anions are the same,the acidities of ILs meet the order:introduction of alkyl sulfonic groups>introduction of alkyl> no introduction;(b) The anion of the ionic liquid mainly affects the esterification and catalytic activity by the acidity mainly through the introduced groups;while the intermiscibility of the whole ILs molecule with the esterification reaction system is the key factor to the catalytic activity.%合成了由5种不同阳离子和2种不同阴离子组成的3类2-甲基吡啶类离子液体;采用FT-IR和UV-vis对所制备的离子液体进行了结构和酸性表征,考察了离子液体的结构与其酸性的关联,并以癸酸和三聚甘油的酯化反应为探针反应,考察了离子液体的酯化催化性能.结果表明:(a)阳离子结构相同时,离子液体酸性与阴离子酸性一致,即HSO4-> H2PO4-;阴离子结构相同时,3类离子液体酸性满足:引入烷基磺酸基>引入烷基>未引入;(b)阴离子主要通过酸性影响酯化催化活性,阳离子主要通过引入的基团影响酯化催化活性;而整个离子液体结构导致的与酯化反应体系的相溶性是影响催化活性的主要因素.
    • 杨颖; 范开功; 白鹏; 郭翔海
    • 摘要: 采用共沸精馏的方法分离2-甲基吡啶和水二元均相共沸物系.选取环己烷作为共沸剂,利用流程模拟软件Aspen Plus对共沸精馏塔进行模拟计算,分析了不同共沸剂用量、塔底采出量以及进料位置等操作参数对产品纯度、共沸剂的损失量以及精馏塔热负荷的影响,模拟结果表明当精馏塔的塔板数为21,共沸剂的用量为3600kg/h,塔底采出量为888kg/h,原料进料位置在第15块板时,共沸精馏塔塔底可得到质量分数为99.54% 的2-甲基吡啶,塔顶分相罐下层可采出质量分数为99.97% 的水.最后,通过间歇共沸精馏实验对以环己烷为共沸剂分离2-甲基吡啶-水物系的效果进行检验,结果表明共沸精馏塔塔底2-甲基吡啶的质量分数达99.85%,塔顶水相可采出质量分数达99.96%的水,证明了该工艺路线具有良好的可行性.%Azeotropic distillation was used to separate 2-methylpyridine and water azeotropic mixture. First,cyclohexane was chosen as the azeotropic entrainer. Second,Aspen Plus were used to simulate the continuous azotropic distillation process. The effects of entrainer flow rate and output quantity at the bottom and feed location on the product purity and heat duty were analyzed to get the optimal operation parameters. The result indicated that when the theoretical stage number was 21,the entrainer flow rate was 3600kg/h,the output quantity at the bottom was 888kg/h,and the feed location was 15, the purity of 2-methylpyridine and water can achieve as 99.54% and 99.97%,respectively. Finally,in order to investigate the effectiveness of the solvent,the batch azeotropic distillation experiments were carried out. The results showed that the purity of 2-methylpyridine and water can achieve as 99.85% and 99.96%,respectively,which revealed that cyclohexane was an ideal azeotropic agent and the azeotropic distillation was useful in the separation of 2-methylpyridine and water system.
    • 肖尚友; 毕旌富; 穆小静; 周曌; 徐广
    • 摘要: Alkyl aza-arene derivatives were synthesized in high-temperature water without catalyst.The effects of temperature,reaction time,molar ratio of reactants and amount of water on the reaction were investigated.The results indicate that it is an efficient way to synthesize 2-methylquinoline derivatives and 2-methylpyridine derivatives from 2-methylquinoline and 2-methylpyridine with various aromatic aldehydes by C-H bond activation.This process is clean and easy to operate.%以高温水为溶剂,在不加催化剂的条件下合成了烷基氮杂芳烃衍生物.研究了反应温度、反应时间、反应物比例和水的用量对收率的影响.实验结果表明,通过C-H键的活化,2-甲基喹啉及2-甲基吡啶可以和各种芳香醛反应,合成2-甲基喹啉衍生物及2-甲基吡啶衍生物.该法无污染,且易于后处理.
    • 高帅鹏; 黄飞; 张静; 史保贵
    • 摘要: 研究建立了活性炭管吸附,甲醇解吸,气相色谱法测定环境空气中2-甲基吡啶的方法.该法的检出限为1.8×10-3 mg/m3,线性相关系数r为0.999 6,精密度RSD为1.3%~2.9%,回收率为82%~84%.该方法简单,干扰较少,结果准确、可靠,重现性好,适用于环境空气中2-甲基吡啶的测定.%A simple and sensitive gas chromatography method for determining 2-Picoline in air ambient was established which activated by carbon tubes and desorpted by methanol.The detect limits of this method is consistently bellowed 1.8×10-3 mg/m3, the linear correlated coefficient(r)is 0.999 6, and with recoveries from are ranged 82% to 84%, and the RSD was between 1.3% and 2.9%.The method is simple,less interference,accurate and highly reproducible, suitable for determining the 2-Picoline in air ambient.
    • 王立升; 张森; 刘华文; 李东; 刘旭
    • 摘要: 以2-甲基吡啶为原料,经氧化、硝化、还原反应合成了重要中间体4-氨基-2-甲基吡啶(3);3分别经1,4-加成反应、Heck反应及取代反应合成了11个吡啶类化合物(4~14),其中5,6和8~14为新化合物,其结构经1 H NMR,13 C NMR, MS和HR-MS进行表征。%4-Amino-2-methylpyridine (3) were synthesized by oxidation , nitration and reduction using 2-methyl pyridine as a raw material .Eleven pyridine compounds (4~14) were synthesized by 1,4-ad-ditive reaction, Heck rection and substitution reaction using 3 as an important intermediate .Among them, 5, 6 and 8 ~14 were new compounds .The structures were characterized by 1 H NMR, 13 C NMR, MS and HR-MS.
    • 魏梦怡; 祁超; 杨建平; 钱超; 陈新志
    • 摘要: 用混合法制备了含有五氧化二钒(V2O5)、二氧化钛(TiO2)和三氧化钼(MoO3)的三元催化剂,用于连续气固相氨氧化2-甲基吡啶合成2-氰基吡啶.结果表明,助催化组分三氧化钼(MoO3)能提高2-氰基吡啶的选择性,当催化剂组成为8.91%(wt) V2O5、85.84%(wt) TiO2和5.25%(wt) MoO3时2-氰基吡啶的选择性最好.基于改进后的V-Ti-O-Mo催化剂,对2-甲基吡啶的氨氧化反应工艺条件进行了优化,当反应温度380°C、物料配比1∶5∶3.3∶22(2-甲基吡啶/氨气/水/空气,摩尔比)、空速0.15 h-1时,2-氰基毗啶收率达到最优值85.6%.
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