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The copolymerizations of ethylene with 10-undecen-1-ol have been investigated using vanadium precatalysts, bis(imino)pyrrolyl vanadium(Ⅲ) complexes 1-3, 2,5-C4H2N(CH=NR)2VCl2(THF)2 [R = C6H5 (1), 2,6-iPr2C6H3 (2), C6F5 (3)], and the iminopyrrolyl and b-diketiminate ones for comparison. The polar monomer was pretreated by diethylaluminium chloride (present also as the cocatalyst) before the copolymerization. The monomer reactivity ratios were evaluated using the Fineman-Ross method. The ligand structure considerably influenced the catalytic activity and tolerance towards the polar monomer, the polar monomer incorporation and the molecular weights of the resultant copolymers. The bis(imino)pyrrolyl vanadium complexes exhibited promising catalytic performance for the copolymerization, and a high catalytic activity up to 3.84 kg/mmolv·h with a high comonomer incorporation of 14.0 mol% was achieved by complex 3 under mild conditions. 相似文献
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火焰原子吸收法测定山楂叶中钙、锰、铁、锌、镁、铜、铅、铬的含量 总被引:4,自引:0,他引:4
对广西山楂叶进行湿法消化处理,利用火焰原子吸收分光光度法测定了其中微量元素的含量。结果表明,山楂叶中含有较丰富的Ca、Mg、Fe、Mn。该法的加标回收率为99.6%~105.0%,RSD≤0.71%,测定结果准确。 相似文献
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合成了一系列高分子量、窄分子量分布且高等规度,含有不同―NR_3~+X~-离子基团含量的聚丙烯离聚体(iPP-NR_3~+X~-).以PP/IUD共聚物作为反应中间体,与三乙胺或N-甲基咪唑氨化得到聚丙烯离聚体.通过离子交换反应制备不同反离子的N-甲基咪唑聚丙烯离聚体,包括双三氟甲基磺酰亚胺根离子(Tf_2N~-)、四氟硼酸根离子(BF_4~-)和六氟磷酸根离子(PF_6~-).热重分析结果发现N-甲基咪唑聚丙烯离聚体的热稳定性明显优于三乙胺聚丙烯离聚体,表明不含β-H的N-甲基咪唑聚丙烯离聚体具有较高的热稳定性.同时,聚丙烯离聚体的表面亲水性得到明显改善.并且,聚丙烯离聚体的断裂伸长率也得到显著提高,最高达到900%.比较不同反离子聚丙烯离聚体的屈服强度和断裂强度发现I~-聚丙烯离聚体具有最优的力学性能. 相似文献
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Novel copolymerization of ethylene with substituted allenes(CH2=C = CH—R,1:R = n-butyl,2:R =n-octyl) using bis(β-enaminoketonato)titanium catalysts[PhN = C(R2)CHC(R1)O]2TiCl2(1a:R1 = CF3,R2 = CH3;1b:R1 = Ph,R2 = CF3) has been investigated.In the presence of modified methylaluminoxane,these catalysts can copolymerize ethylene with substituted allenes,affording copolymers with unimodal molecular weight distributions and homogeneous compositions.By varying the reaction conditions,the comonomer incorporation can be tuned in the range of 0-3.6 mol%.1H-NMR spectra reveal that the copolymerization proceeds through 1,2-insertion fashion of allene comonomer exclusively,and the regioselective nature maintains under various reaction conditions.The retained intra-chain double bond can be converted into the epoxy group under mild conditions. 相似文献
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Mono salicylaldiminato vanadium(Ⅲ) complexes(1a-1f)[RN = CH(ArO)]VCl2(THF)2(Ar = C6H4(1a-1e),R = Ph,1a;R = p-CF3Ph,1b;R = 2,6-Me2Ph,1c;R = 2,6-iPr2Ph,1d;R = cyclohexyl,1e;Ar = C6H2tBu2(2,4),R = 2,6-iPr2Ph, 1f) and bis(salicylaldiminato) vanadium(Ⅲ) complexes(2a-2f)[RN = CH(ArO)]2VCl(THF)x(Ar = C6H4(2a-2e),x = 1 (2a-2e),R = Ph,2a;R =p-CF3Ph,2b;R = 2,6-Me2Ph,2c;R = 2,6-iPr2Ph,2d;R = cyclohexyl,2e;Ar = C6H2tBu2(2,4),R = 2,6-iPr2Ph,x = 0,2f) have been evaluated as the active catalysts for ethylene/1-hexene copolymerization in the presence of Et2AlCl.The ligand substitution pattern and the catalyst structure model significantly influenced the polymerization behaviors such as the catalytic activity,the molecular weight and molecular weight distribution of the copolymers etc.The highest catalytic activity of 8.82 kg PE/(mmolV·h) was observed for vanadium catalyst 2d with two 2,6-diisopropylphenyl substituted salicylaldiminato ligands.The copolymer with the highest molecular weight was obtained by using mono salicylaldiminato vanadium catalyst 1f having ligands with tert-butyl at the ortho and para of the aryloxy moiety. 相似文献
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研究了利用N-乙酰-L-谷氨酸为拆分试剂,成功的对氯化3-氰-2-羟丙基三甲胺进行光学拆分,一次拆分光学纯度为92%,产率为37%;二次拆分光学纯度达95%,产率为29.1%。 相似文献
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以氧化铝和二氧化硅作为原料,二氧化锰作为添加剂,在烧结温度1300℃时,研究了不同二氧化锰添加量制备所得试样的结构和性能,通过对试样物相组成、显微结构、体积密度、显气孔率和抗折强度五方面的分析,研究了二氧化锰作为添加剂对莫来石相的形成、发育和性能的影响,并分析了莫来石相形成和发育过程中二氧化锰的作用机理.结果表明:MnO2的添加能促进固相烧结反应,降低烧结温度,抑制石英相的生长,促进莫来石相的形核和发育.同时在烧结过程中Mn4+能够加快晶粒生长. 相似文献
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