琥珀酸酯为内给电子体的新型MgCl2载体催化剂用于丙烯聚合

A novel MgCl_2-supported Ziegler-Natta catalyst containing diethyl diisopropylsuccinate donor was pre- pared and propylene polymerizations with the combination of such catalyst and four external donors were inves- tigated in detail.The catalyst was compared with a commercial one with phthalate as internal donor in terms of catalytic activity,hydrogen sensitivity and stereospecificity in propylene polymerization.The molecular weight, molecular weight distribution and microstructure of the produced polypropylenes were compared also.It was found that the novel catalyst containing succinate internal donor showed higher activity and higher stereospecificity than those with phthalate as internal donor.Consequently,polypropylenes obtained by the succinate-based catalyst showed high molecular weight,high melting temperature,high isotactic index and broad molecular weight distribu- tion than those obtained with the commercial catalyst.     

新型高性能Ziegler-Natta催化剂用于乙烯淤浆聚合

A novel high performance MgCl2/TiCl4 catalyst with tetrabutyloxsilicane as electron donor was prepared for ethylene slurry polymerization process. The properties of the catalyst such as particle size distribution, catalytic activity, hydrogen responsibility and copolymerization performance were investigated and compared with commercial catalyst (imported catalyst). Copolymerization of ethylene and 1-butylene using the catalyst was stud-ied in a pilot plant. The composition, structure and property of the copolymer were characterized by 13C nuclear magnetic resonance (13C NMR) and gel permeation chromatography-Infrared (GPC-IR), and compared with those of the copolymer obtained from a commercial catalyst. In comparison with the commercial catalyst, the novel cata-lyst had a higher activity (up to 34.6 kg•g－1) and a better particle size distribution (PSD), and produced polymers having higher bulk density (up to 0.37 g•cm－3) with less fine resin. Meanwhile, the novel catalyst showed a higher hydrogen responsibility and better copolymerization performance. The results indicated that the copolymer obtained from the novel catalyst has a higher branch in the high molecular weight fraction and lower branch in the low mo-lecular weight fraction.     

金属担载分子筛对含硫模型化合物和含硫烃的催化裂化脱硫反应的影响

Zn, La, Zr, Sn and Ti loaded molecular sieves were prepared by impregnation method. Conversions of benzothiophene and dibenzothiophene over the metal oxides modified ultra stable zeolite Y(USY), ZSM-5, β and MSU-2 molecular sieve catalysts were investigated by means of micro-activity test (MAT) experiments. The results showed that Zn and La loaded catalysts were better than the other metals, and ZSM-5 with lower SiO2/Al2O3 mole ratio showed better results than those with higher SiO2/Al2O3 as far as desulfurization reaction is considered. A comparison of the desulfurization activities of the La/Zn-USY catalyst with USY catalyst indicated that the bimetal loaded USY catalyst gave good products selectivity when sulfur containing heavy oil was used as the feedstock. The sulfur content in gasoline fraction was decreased by 25%, and there was no loss in the Research Octane Number.     

专虑(火用)和熵而得到的催化剂粒内活性最优分布

It is generally recognized that the optimal distribution of catalyst activity in a spherical catalyst is a Dirac δ-function. However, catalyst with other alternative distribution may accomplish the same reaction task without necessarily concentrating the catalyst activity in an inside thin layer.Moreover, the alternative with activity on catalyst surface may offer higher reaction rate and better utilization of reaction heat (higher exergy output). Simple cases of first-order exothermal reactions, in particular when the catalyst is limited by the maximum working temperature, are presented to demonstrate the above advantages and to show the importance of studying the optimal activity distribution with the consideration on exergy maximization and entroov oroduction minimization.     

超硬材料磨具用烯丙基化酚醛改性双马来酰亚胺树脂的研究

A novel thermosetting resin system for superabrasives based on novolak and bismaleimide （BMI） was developed. The novolak resin was allylated and then copolymerized with BMI. The structure of allyl novolak and reaction mechanism were analyzed by FFIR. Thermal and mechanical properties were characterized by using com- prehensive thermal analyzer （DSC-TG） and strength tester, respectively. The results showed that high molecular weight of novolak was advantageous for heat-resistance, but was unfavorable for the bending strength. High allyl content improved the heat-resistance but lowered the bending strength. When the molecular weight of novolak was 450 and allyl content was 50%, the best resin system with good heat-resistance and bending strength was obtained. It was suitable for the manufacturing of superabrasive tools.     

Characterization of pyrolytic lignins with different activities obtained from bio-oil

Pyrolytic lignin, the water-insoluble fraction in bio-oil, often shows a high content and has strong intermolecular interactions with other compounds in bio-oil. In order to obtain pure pyrolytic lignin and facilitate the utilization of aqueous phase obtained from water extraction of bio-oil, methanol–water extraction method was employed to further separate the bio-oil water-insoluble phase in this paper. Different technologies, including Fourier transform infrared spectroscopy, gel permeation chromatography, and nuclear magnetic resonance, were adopted to characterize the structures of pyrolytic lignins with different activities obtained through this method. Both the heating value and the polymerization degree of high-molecular-weight pyrolytic lignin were higher than those of low-molecular-weight pyrolytic lignin. The molecular weight distribution of high-molecular-weight pyrolytic lignin was relatively wider, among which the contents of dimers to pentamers all accounted for 12% –18%,while the low-molecular-weight pyrolytic lignin mainly consisted of trimers(75.38%). The pyrolytic lignins had similar basic structures, both of which contained syringyl and guaiacyl units, whereas the low-molecular-weight pyrolytic lignin had more abundant syringyl units, reactive carbonyl groups and hydroxyl groups. Meanwhile,thermogravimetric study revealed that the final char residue yield of low-molecular-weight pyrolytic lignin was lower than that of high-molecular-weight pyrolytic lignin.     

Functionalized metal–organic frameworks with strong acidity and hydrophobicity as an efficient catalyst for the production of 5-hydroxymethylfurfural

In the dehydration of fructose to 5-hydroxymethyl furfural(HMF), in situ produced water weakens the acid strength of the catalyst and causes the rehydration of HMF, causing unsatisfactory catalytic activity and selectivity. In this work, a class of benzenesulfonic acid-grafted metal–organic frameworks with strong acidity and hydrophobicity is obtained by the direct sulfonation method using 4-chlorobenzenesulfonic acid as sulfonating agent. The resultant MOFs have a specific surface area of greater than 250 m~2·g~(-1), acid density above 1.0 mmol·g~(-1), and water contact angle up to 129°. The hydrophobic MOF-Ph SO_3 H exhibits both higher catalytic activity and selectivity than MOF-SO_3 H in the HMF synthesis due to its better hydrophobicity and olephilicity. Moreover, the catalyst has a high recycled stability. At last, fructose is completely converted, and 98.0% yield of HMF is obtained under 120 °C in a DMSO solvent system. The successful preparation of the hydrophobic acidic MOF provides a novel hydrophobic catalyst for the synthesis of HMF.     

改进的催化剂的乙烯聚合动力学研究

The study concerns the use of MgCl2-supported high-activity Ziegler-Natta catalysts for the polymerization of ethylene. In particular, two types of catalysts were investigated, which were N-catalyst (BRICI) and improved polyethylene catalyst. The effects of catalyst structure on kinetic behavior were examined. The distribution of active centers in these catalysts was investigated by energy dispersive analysis by X-rays (EDAX), and morphologies of catalyst particles and polymer products were examined by scanning electron microscope (SEM). Hydrogen response and copolymerization performance were investigated and compared with the two catalysts. The results were correlated with the kinetic behavior of the two catalysts and appropriate models for polymer particle growth were presented. The improved polyethylene catalyst showed higher activity, better hydrogen response and copolymerization performance.     

蒸汽诱导相分离法制备具有规整微孔结构的聚醚砜膜(英文)

Polyethersulfone(PES)film with regular microporous structure was formed using dichloromethane as the solvent via water vapor induced phase separation(VIPS).The effects of solution concentration,atmospheric humidity and temperature,as well as molecular weight of PES on the surface morphology of the polymer film were investigated.The surface morphology characterized by SEM showed that the pore size reduced as the solution concentration increased.There was an optimum range of relative humidity for the formation of regular pore structure, which was from 60%to 90%at concentration of 20 g·L-1 and 20°C.With the atmospheric temperature varied from 20 to 30°C,the pore became larger and the space between pores increased.The pore size in the PES film with low molecular weight was smaller than that with high molecular weight.     

新型超细包覆型催化剂的制备及催化苯酚氧化羰基化合成碳酸二苯酯

A novel catalytic material, ultrafine silica embedded catalyst, was prepared through the hydrolysis of tetraethoxysilane (TEOS) in W/O microemulsion, which was composed of cyclohexane,polyoxyethylene (10) nonylphenyl (NP-10), hexanol and aqua ammonia of PdC12 and Cu(OAc)2. It was found that the active species was wholly or partly embedded in the spherical silica particles with diameters in the range of 40-120 nm. The catalytic behavior of the catalyst in oxidative carbonylation of phenol to diphenyl carbonate (DPC) was studied. Under the optimized conditions (80℃, 3. 9 MPa and 8 h), the yield of DPC was 35. 4%. In comparison with the catalysts prepared by the impregnation and sol-gel method, the ultrafine embedded catalyst showed high activity and long service time. When the catalyst was used at 80℃, 3.9 MPa and 4 h for 4 times, the yield of DPC was 25. 2%, 16.5%, 14. 5% and 13.4%, respectively.     

Novel MgCl2-supported catalyst containing diol dibenzoate donor for propylene polymerization

A novel MgCl₂-supported Ziegler-Natta catalyst containing 2-isoamyl-2-isopropyl-1,3-propandiol dibenzoate donor for propylene polymerization was studied, and compared with catalysts with different internal donors, such as benzoate, phthalate and diether, in polymerization dynamic behavior, activity, hydrogen response and stereospecificity. It was found that there are two highly isospecific active sites in the catalyst with dibenzoate internal donor system and the effections of temperature are different on the performances of the two highly isospecific sites.     

MgCl2‐supported catalyst containing mixed internal donors for propylene polymerization

A MgCl₂‐supported catalyst containing diisobutyl phthalate (DIBP) and 2,4‐pentadiol dibenzoate (PDDB) as internal donors was prepared. Propylene polymerizations were carried out using the catalyst in the absence or presence of an external donor. The resulting polymers were characterized by ¹³C‐NMR, crystallization analysis fraction (CRYSTAF) and gel permeation chromatography (GPC). The performance of the catalyst was compared with that of other catalysts containing donor‐free, DIBP and PDDB as internal donors respectively. The results demonstrated that the catalyst containing mixed internal donors not only had high activity and stereospecificity but also produced the polymer with relatively broad molecular weight distribution and the highest [mmmm] value. ¹³C‐NMR analysis results indicated that strongly coordinating donors gave more stereoregular polymers, which was further confirmed by CRYSTAF data. The effects of mixed internal donors on the catalyst properties were discussed systematically. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Copolymerization of ethylene and propylene catalyzed by novel magnesium chloride supported,vanadium‐based catalysts

Two novel magnesium chloride supported, vanadium‐based Ziegler–Natta catalysts with 9,9‐bis(methoxymethyl)fluorene and di‐i‐butyl phthalate as internal donors were prepared and used in the copolymerization of ethylene and propylene. The catalytic behaviors of these catalysts were investigated and compared with those of traditional magnesium chloride supported, vanadium‐based catalysts without internal donors. Differential scanning calorimetry, gel permeation chromatography, and ¹³C‐NMR spectroscopy analysis were performed to characterize the melting temperatures, molecular weights, and molecular weight distributions as well as structures and compositions of the products. The copolymerization kinetic results indicated that the novel catalyst with 9,9‐bis(methoxymethyl)fluorene as an internal donor had the highest catalytic activity and optimal kinetic behavior in ethylene–propylene copolymerization with an ethylene/propylene molar ratio of 44/56. Low‐crystallinity and high‐molecular‐weight copolymers were obtained with these novel magnesium chloride supported, vanadium‐based catalysts. The reactivity ratio data indicated that the catalytic systems had a tendency to produce random ethylene–propylene copolymers. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

二醇酯类内给电子体丙烯聚合反应催化剂的研究进展

综合介绍了目前丙烯聚合反应催化剂研究热点非邻苯二甲酸酯类催化剂之一--二醇酯类催化剂的研发进展情况, 讨论了以此类化合物为内给电子体的系列催化剂的性能, 对该类催化剂在不同聚丙烯工艺生产中的聚合物性能与邻苯二甲酸酯类催化剂进行了比较, 重点研究了不同结构的二元醇酯类内给电子体化合物对所得催化剂性能的影响, 发现化合物结构中较大取代基团的存在可使所得催化剂的活性及定向能力提高, 结构中取代基团的大小及其位置对所得催化剂的氢调敏感性能有影响。该二醇酯类催化剂符合绿色与环保要求, 所生产聚合物的力学性能好, 具有较好的发展前景。     

The influence of cocatalysts on 1-hexene polymerization with various supported magnesium – titanium catalysts

Summary The influence of various cocatalysts on the activity and stereospecificity of a supported magnesium–titanium catalyst, generated by in situ reduction of titanium (IV) chloride using a Grignard reagent (MgCl₂/TiCl₃) or prepared by the recrystallization method (MgCl₂/2M2P/ED/TiCl₄, 2M2P= 2-methyl-2-pentanol, ED= dibutyl phthalate or ethyl benzoate), in the 1-hexene polymerization was investigated. The MgCl₂/TiCl₃ catalyst showed the highest activity but the lowest stereospecificity in the 1-hexene polymerization with all investigated cocatalysts. The MgCl₂/2M2P/ED/TiCl₄ catalyst with dibutyl phthalate as an internal electron donor was characterized by the highest stereospecificity and led to the polymers with high molecular weight. All catalysts showed the highest activity and stereospecificity when triisobutylaluminium was used as a cocatalyst. The addition of a small amount of ethyl benzoate as an external electron donor ([Al]/[ED] 10:1) led to considerable improvement of the stereospecificity of the MgCl₂/TiCl₃ catalyst in comparison with the catalysts prepared by the recrystallization method.     

Preparation of bimodal polypropylene in two‐step polymerization

Polymerization of propylene was carried out by using MgCl₂.EtOH.TiCl₄.DIBP.TEA.cHMDMS catalyst system in n‐heptane, where MgCl₂, EtOH, TiCl₄, DIBP (diisobutyl phthalate), TEA (triethyl aluminum), and cHMDMS (cyclohexyl methyl dimethoxy silane) were support, ethanol for alcoholation, catalyst, external donor, cocatalyst (activator), and internal donor, respectively. The catalyst activity and polymer isotacticity were studied by measuring the produced polymer and its solubility in boiling n‐heptane, respectively. The molecular weight and molecular weight distribution of the polymers were evaluated by gel permeation chromatography. Hydrogen was used for controlling the molecular weight. For producing the bimodal polypropylene, the polymerization was carried out in two steps (i.e., in the presence and absence of hydrogen). It was found that the catalyst showed high activity and stereoselectivity, on the other hand, bimodal polymer could simply be produced in two‐step polymerization by using MgCl₂.EtOH.TiCl₄.DIBP.TEA.cHMDMS catalyst system. Meanwhile, the effect of the step of the hydrogen adding on propylene polymerization was investigated. It was shown that the addition of hydrogen in the second step was more suitable. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1456–1462, 2006     

Propylene polymerization using supported Ziegler–Natta catalyst systems with mixed donors

Magnesium dichloride supported titanium catalyst incorporated with varying concentration of ethylbenzoate and diisobutyl phthalate together as internal donor are synthesized. The synthesized catalysts are characterized and compared with respect to composition, phase characteristics, crystallite size, and particle morphology. Performance of catalysts containing mixed donors is compared with the conventional single donor-based catalysts. The polymerization studies of the catalysts for propylene polymerization show dependence of polymerization kinetics on relative concentration of diisobutyl phthalate and ethylbenzoate. Molecular weight characteristics of polypropylene obtained from these catalysts are studied and correlated with the nature and concentration of donors present in the catalyst. Morphology replication from catalyst precursor to polymer is observed irrespective of the nature of donor being incorporated in the synthesized catalyst. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Control of molecular weight distribution for polypropylene obtained by a commercial Ziegler–Natta catalyst: Effect of a cocatalyst and hydrogen

The polymerization of propylene was carried out with an MgCl₂‐supported TiCl₄ catalyst (with diisobutyl phthalate as an internal donor) in the absence and presence of hydrogen (H₂) as a chain‐transfer agent. Different structures of alkylaluminum were used as cocatalysts. The effects of the alkyl group size of the cocatalyst, H₂ feed, and feed time on the propylene polymerization behaviors were investigated. The catalyst activity significantly decreased with increasing alkyl group size in the cocatalyst. The molecular weight and polydispersity index (PDI) increased with increasing alkyl group size. With the introduction of H₂, the catalyst activity increased significantly, whereas the molecular weight and PDI of polypropylene (PP) decreased. Additionally, the effect of the polymerization time in the presence of H₂ on the propylene polymerization was studied. The molecular weight distribution curve was bimodal at short polymerization times in the presence of H₂, and we could control the molecular weight distribution of PP by changing the polymerization time in the presence of H₂. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011