Graft Polymerization of Methyl Methacrylate- Acrylonitrile onto Poly(ethene-co-1-butene) and Its Toughening Effect on SAN Resin

Poly(ethene-co-1-butene)-graft-methyl methacrylate-acrylonitrile (PEB-g-MAN) was prepared by suspension grafting copolymerization of methyl methacrylate (MMA) and acrylonitrile(AN) onto PEB. PEB-g-MAN/SAN resin blends (ABMS) were prepared by blending PEB-g-MAN with styrene-acrylonitrile copolymer (SAN resin). The effects of AN/(MMA+AN) feed ratio (f_AN), PEB/(PEB+MMA+AN) feed ratio (f_PEB) and benzoyl peroxide (BPO) dosage on the monomer conversion ratio (CR), rubber's grafting ratio (GR), grafting efficiency (GE) of the copolymerization and the toughening effect of PEB-g-MAN on the SAN resin were investigated. FTIR quantitative analysis showed that when the weight percent of AN unit in the unextracted product was 21.5 wt% with f_AN of 25 wt%, the toughening effect of unextracted PEB-g-MAN on SAN resin was the highest. Gel permeation chromatography (GPC) analysis showed that when f_AN was 25 wt%, the grafted copolymer had the lowest molecular weight and ABMS had highest toughness. Transmission electron microscopy (TEM) analysis showed that the highest toughness occurred when the phase structure of ABMS was cocontinuous with f_AN of 25 wt%. When f_AN was 25 wt% PEB-g-MAN domains have numerous small SAN domains in them, which was occlusion structure. Scanning electron microscopy (SEM) analysis indicated that the ABMS fracture surfaces had plastic flow visible, which looked like a craze fibers morphology, for the sample with highest impact strength (f_AN = 25 wt%). Dynamic mechanical thermal analysis (DMA) showed that the miscibility of the PEB phase and SAN phase improved after graft copolymerization of MMA and AN onto PEB.     

Preparation and Properties of Polyethylene Terephthalate (PET)/Near Infrared Reflective Pigment (NIR) Composites

A near infrared reflective (NIR, nickel antimony titanium yellow rutile) pigment filler was incorporated into a polyethylene terephthalate (PET) matrix via a melt blending approach to increase the infrared reflection of PET and limit the thermal heat accumulation in light of environmental and energy conservation concerns. Two different types of surface modifiers, polyethylene glycol (PEG) and cetyltrimethylammonium bromide (CTAB), were used to modify the NIR surface, as NIR–PEG and NIR–CTAB fillers, to investigate the surface modification effect. Fourier transform infrared spectroscopy (FTIR), a Zetasizer, and electron spectroscopy for chemical analysis (ESCA) results suggested a successful adsorption of the organic modifiers onto the NIR surface. Thermogravimetric analysis indicated a higher adsorption degree for the CTAB modifier than the PEG modifier due to the electronic interaction between CTAB and NIR. The thermal crystallization temperature (T_c) for neat NIR-filled samples decreased with increasing NIR content within the PET matrix at first, up to 9°C, but then tended to increase again up to a measurable difference of 6°C with respect to pure PEG, indicating the promotion of the crystallization kinetics of the neat NIR within the PET matrix. On the other hand, a decrease in T_c for all NIR-CTAB or NIR-PEG loadings was found, with the depression close to 10°C for all NIR-CTAB samples regardless of the loading. CTAB modified NIR gave the highest improvement in tensile strength and strain at break in comparison with NIR and NIR-PEG filled samples. The near infrared reflection values of modified PET were higher than those of neat PET. The reflection values appeared to be the highest for some concentrations of the NIR-CTAB filled samples, but were of similar orders of magnitude with those for NIR or NIR-PEG filled samples.     

Further results on the euler and Genocchi numbers

Summary We characterize the ordinary generating functions of the Genocchi and median Genocchi numbers as unique solutions of some functional equations and give a direct algebraic proof of several continued fraction expansions for these functions. New relations between these numbers are also obtained.     

可能性理论的推广方法及合理性研究

本文通过引入二维可能性分布函数的概念，将可能性测度推广到二维的情形。并给出了二维可能性测度的一些重要性质。文中还重点证明了该推广方法的合理性。     

HOMOCLINIC SOLUTIONS FOR AUTONOMOUS DIFFERENTIAL EQUATIONS

ＨＯＭＯＣＬＩＮＩＣ　ＳＯＬＵＴＩＯＮＳ　ＦＯＲ　ＡＵＴＯＮＯＭＯＵＳ　ＤＩＦＦＥＲＥＮＴＩＡＬ　ＥＱＵＡＴＩＯＮＳ￥ＺｅｎｇＷｅｉｙａｏ（曾唯尧）（ＨｕｎａｎＬｉｇｈｔＩｎｄｕｓｔｒｉａｌＣｏｌｌｅｇｅ）＆ＷａｎｇＸｕｅｘｉｎ（王学鑫）（Ｚｈｅｊｉ...     

指数型二分性与拟自治奇异摄动系统

通过对Ｋ．Ｊ．Ｐａｌｍｅｒ￣［４］中方法的改进，本文讨论了摄动系统有界解的存在性，得到了不同于［４］中的结果，并把改进了的方法运用到拟自治奇异摄动系统，得到了拟自治奇异摄动系统存在有界解的一个简洁的充分条件。本文的方法还提供了一个处理摄动项含小参数的方法。     

激光产生温稠密物质的微观动力学过程及状态诊断

随着大型激光装置的建立和精密测量技术的发展,强激光与固体相互作用成为实验室产生温稠密物质的一个重要手段。温稠密物质的结构复杂性、瞬态性和非平衡性给理论建模和实验测量带来了巨大挑战。本文系统介绍了激光产生温稠密物质的实验手段和理论模拟方法方面的重要进展,分析了其中的电子激发动力学、电子-离子能量弛豫过程、离子动力学等物理过程,总结了温稠密物质状态诊断的实验技术和理论方法,并论述了激光产生温稠密物质的发展趋势。     

基于锥面衍射实现高效率双光栅光谱合成

分析了基于锥面衍射的双光栅光谱合成系统的可行性,设计了激光入射角为Littrow角附近的双多层介质膜（MLD）光栅光谱合成系统,开展了两路合成实验。当入射极角等于自准直入射角,入射方位角为6°时,光栅衍射效率近似等于光束自准直入射时的衍射效率。基于锥面衍射原理,对中心波长为1050.24 nm和1064.33 nm的两束光纤激光子束进行合成,入射极角为43.99°,测得合成效率为92.9%,较基于非锥面衍射的双光栅光谱合成系统的合成效率提高了8.8%;测得合成光斑光束质量M_x²＝1.204,M_y²＝1.467,与基于非锥面衍射的双光栅光谱合成系统输出光斑光束质量基本一致。     

A Shell-by-Shell Approach for Synthesis of Mesoporous Multi-Shelled Hollow MOFs for Catalytic Applications

Over the past two decades, advanced materials with hollow interiors have received significant attention in materials research owing to their great application potential across a vast number of technological fields. Though with great difficulty, multi-shelled hollow metal–organic frameworks (MSHMs) have also been successfully synthesized in recent years. Herein, a rational shell-by-shell soft-templating protocol has been devised to fabricate highly uniform multi-shelled hollow cobalt-imidazole-based MOF (ZIF-67). For the first time, it has become possible to endow mesoporosity to this new type of functional material (i.e., mesoporous MOFs). When used as carrier materials in catalytic reactions, in principle, these mesoporous MSHMs with high surface area not only improve the dispersity of metal nanoparticles (NPs), but also efficiently facilitate the mass diffusion of the reactions, resulting in enhanced catalyst activity. Moreover, the obtained MSHMs/M nanocomposites serve as base-metal bifunctional catalysts for one-pot oxidation-Knoevenagel condensation cascade reaction, in which the MSHMs itself serves as a pristine active catalyst in addition to its role of catalyst support. The results demonstrate that excellent multifunctional catalysts can be achieved via preparing intrinsically microporous bulk MOFs into extrinsically mesoporous MSHMs which possess many structural merits that conventional bulk MOFs do not have.