KC型第三代推动篦冷机的开发设计及其特点

前言 从我国水泥生产技术的发展来看，由于第二代以及不带热端固定床的第三代推动篦式冷却机均存在高温端部容易漏料、篦饭寿命短、篦板结构形式的缺陷使得其冷却效率差、易出现“红河”、二三次风温低、冷却风量偏大、动力消耗大、热回收效率低等一系列不尽人意之处。我院存对同外有关技术的消化吸收和实验研究的基础上，通过不断开发、优化，     

Influence of polymerization conditions on the structure and properties of polyethylene/polypropylene in‐reactor alloy synthesized in the gas phase with a spherical Ziegler–Natta catalyst

A spherical TiCl₄/MgCl₂‐based catalyst was used in the synthesis of in‐reactor polyethylene/polypropylene alloys by polyethylene homopolymerization and subsequent homopolymerization of propylene in the gas phase. Different conditions in the ethylene homopolymerization stage, such as monomer pressure and polymerization temperature, were investigated, and their influences on the structure and properties of in‐reactor alloys were studied. Raising the polymerization temperature is the most effective way of speeding up polymerization and regulating the ethylene content of polyethylene (PE)/polypropylene (PP) alloys, but it will cause a greater increase in the PE‐b‐PP block copolymer fraction (named fraction D) than in the fraction of PP‐block‐PE in which the PP segments have low or medium isotacticity (named fraction A). Although changing ethylene monomer pressure could influence the ethylene content of PE/PP alloys slightly, it is an effective way of regulating the structural distribution. Reducing the monomer pressure will evidently increase fractions A and D. The mechanical properties of the alloys, including impact strength and flexural modulus, can be regulated in a broad range with changes in polymerization conditions. These properties are highly dependent on the amount, distribution, and chain structure of fractions A and D. The impact strength is affected by both fraction A and fraction D in a complicated way, whereas the flexural modulus is mainly determined by the amount of fraction A. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2136–2143, 2006     

Synthesis and properties of polystyrene‐b‐poly(ethylene oxide)‐b‐polystyrene triblock copolymers

A series of well‐defined and property‐controlled polystyrene (PS)‐b‐poly(ethylene oxide) (PEO)‐b‐polystyrene (PS) triblock copolymers were synthesized by atom‐transfer radical polymerization, using 2‐bromo‐propionate‐end‐group PEO 2000 as macroinitiatators. The structure of triblock copolymers was confirmed by ¹H‐NMR and GPC. The relationship between some properties and molecular weight of copolymers was studied. It was found that glass‐transition temperature (T_g) of copolymers gradually rose and crystallinity of copolymers regularly dropped when molecular weight of copolymers increased. The copolymers showed to be amphiphilic. Stable emulsions could form in water layer of copolymer–toluene–water system and the emulsifying abilities of copolymers slightly decreased when molecular weight of copolymers increased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 727–730, 2006     

Graft copolymerization of styrene onto casein initiated by potassium diperiodatonickelate (IV) in alkaline medium

A novel redox system, potassium diperiodatonickelate (Ni(IV))‐casein is used to initiate graft copolymerization of Styrene onto casein under different conditions in aqueous alkaline solution. Graft copolymers with both high grafting efficiency (>98%) and percentage of grafting(>300%) are obtained, which indicated that (Ni(IV))‐casein redox pair is an efficient initiator for this grafting. The effects of reaction parameters, such as monomer‐to‐casein weight ratio, initiator concentration, pH, time, and temperature, are investigated. A tentative initiation mechanism is proposed. The structures and properties of the graft copolymer are characterized by Fourier transform infrared Spectroscopy, X‐ray diffraction diagrams, and Scanning Electron Microscope. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4247–4251, 2006     

A novel method for the preparation of monocarboxyl‐end‐grouped polycaprolactam with an adjustable molecular weight

A novel method was used to synthesize adjustable‐molecular‐weight polycaprolactams with monocarboxyl end groups. The reaction device and conditions are discussed. The products were characterized by Fourier transform infrared spectroscopy, ¹H‐NMR spectroscopy, high‐resolution pyrolysis gas chromatography–mass spectrometry, and wide‐angle X‐ray diffraction. The thermal properties were studied by differential scanning calorimetry and thermogravimetric analysis. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 722–727, 2004     

Capture of gypsy moth,Lymantria dispar (L.), andLymantria mathura (L.) males in traps baited with disparlure enantiomers and olefin precursor in the People's Republic of China

Pheromone traps baited with (+)-disparlure,cis-7,8-epoxy-2methyocta-decane, captured males ofLymantria dispar, L. monacha, andL. mathura in northeastern People's Republic of China.L. dispar responded to the addition of olefin to (+)-disparlure-baited traps in a negative doseresponse manner. Observations on site and seasonal capture ofL. dispar andL. mathura are discussed.Lepidoptera: Lymantriidae.     

有机硫加氢(HDS)催化剂的预硫化

预硫化是HDS、HDN过程中决定催化剂活性的最重要环节。在分析催化剂硫化反应原理、硫化条件、硫化与还原的关系等基础上进一步指出了在工业过程中预硫化的一些原则。     

Study of different effect on foaming process of biodegradable bionolle in supercritical carbon dioxide

Microcellular foaming of biodegradable Bionolle in supercritical CO₂ has been produced. The effects of a series of variable factors, such as saturation temperature, saturation pressure, and depressurization time and step on the foam structures and density, were studied through measurement of density and SEM observation. The experimental results show that higher saturation temperatures lead to an increase in bulk densities; and different depressurization time and step result in different product cell morphology. In addition, at some saturation temperature, the orientation of the cells can be found in the product morphology. XRD experimental results show that the foaming treatment with SC CO₂ increased the crystallinity of Bionolle. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2901–2906, 2006     

Studies on the poly(styrene‐b‐butadiene‐b‐styrene)/clay nanocomposites prepared by melt intercalation

Two types of SBS/OMMT composites are prepared by melt blending using a twin‐screw extruder. An X‐ray diffractometer indicates that polymer chains have intercalated into the gallery of the clay. It is shown in TEM photos that the thickness of the layer aggregate in the SBS1301 matrix is approximately 200 Å, but in the SBS4402 matrix the size of the filler particle is in micrometers. When SBS1301 is intermingled into SBS4402/OMMT, the particle size is reduced obviously. The tensile strength and elongation at break of the nanocomposite, SBS1301/OMMT, increase with the addition of OMMT; and when addition is 5phr, they achieve maximum. A small content of OMMT (less than 5phr) can prevent the deterioration of the mechanical properties of the SBS1301/MMT. In addition, a small content of SBS4402 (less than 20 wt %) can improve the mechanical properties of the SBS1301/OMMT composites. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 146–152, 2005     

提纯乙型脑炎细胞培养疫苗的研究

应用截留分子量10万的超滤系统,将地鼠肾细胞乙型脑炎疫苗浓缩10～20倍,再以差速离心法提纯。所得提纯乙脑疫苗免疫原性及抗原效价均比原制苗明显提高,达到日本提纯苗的水平。经人体接种反应和效果观察表明,提纯苗反应轻微,血凝抗体4倍增长率占100%,GMT258.9,与常规苗相比有非常显著差异。