Novel tin-graphite composites as negative electrodes of Li-ion batteries

For the purpose of obtaining an improved performance of the graphite negative electrode of Li-ion batteries, a novel graphite-tin composite has been synthesized by reduction of tin chloride (SnCl₂) with KC₈ in THF medium. This composite contains nano-sized tin particles dispersed on the graphite surface and free tin aggregates. Lithium electrochemical insertion occurs both in graphite and in tin. An experimental reversible specific charge of 489 mA h g⁻¹ is found stable upon cycling. Such a value is lower than the maximum theoretical one of 609 mA h g⁻¹ suggesting that only a part of tin is involved in the lithium insertion/extraction process. This part of active tin responsible for the stable capacity could be that bound to graphite. To the contrary, free tin aggregates could contribute to an extra capacity that decreases upon cycling in relation with the volume changes that occurs during alloying/dealloying.     

Influence of ZnO nanoparticles on the cure characteristics and mechanical properties of carboxylated nitrile rubber

Zinc oxide (ZnO) nanoparticles assembled in one dimension to give rod‐shaped morphology were synthesized. The effect of these ZnO nanoparticles (average particle size ～ 50 nm) as the curing agent for carboxylated nitrile rubber was studied with special attention to cure characteristics, mechanical properties, dynamic mechanical properties, and swelling. These results were compared with those of the conventional rubber grade ZnO. The study confirmed that the ZnO nanoparticles gave a better state of cure and higher maximum torque with a marginal decrease in optimum cure time and scorch time. The mechanical properties also showed an improvement. There was an increase in tensile strength by ～ 120%, elongation at break by ～ 20%, and modulus at 300% elongation by ～ 30% for the vulcanizate cured with ZnO nanoparticles, as compared with the one containing rubber grade ZnO. Dynamic mechanical analysis revealed that the vulcanizates exhibited two transitions—one occurring at lower temperature due to the T_g of the polymer, while the second at higher temperature corresponding to the hard phase arising due to the ionic structures. The second transition showed a peak broadening because of an increase in the points of interaction of ZnO nanoparticles with the matrix. The tan δ peak showed a shift towards higher T_g in the case of ZnO nanoparticle‐cured vulcanizate, indicating higher crosslinking density. This was further confirmed by volume fraction of rubber in the swollen gel and infrared spectroscopic studies. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Effect of charge density,molecular weight,and hydrophobicity on polycations adsorption and flocculation of polystyrene latices and silica

Adsorption and flocculation behavior of two series of synthetic polycations was investigated in dispersions of silica and polystyrene latices with various particle size and surface charge densities. Polycations of the first series (polydiallyldimethyl ammonium chloride‐PDADMAC) varied in molecular weight only, while polycations of the second series (derivatives of polymethacrylic acid) varied in both molecular weight and hydrophobicity. We have found that maximum adsorbed amount of high molecular weight PDADMAC on latex particles was nearly independent of the surface charge density when the particle size was comparable to the polymer coil dimensions in solution. Both low and high molecular weight PDADMACs were efficient flocculants, although significantly lower amounts of high molecular weight polyelectrolyte were required for the phase separation in the dispersions due to particles aggregation through “charge patch” mechanism. The increase of polymer hydrophobicity leads to higher adsorbed amounts and broadening of flocculation window by polycations of the second series on both substrates. However, no strong enhancement of segment–surface interactions on hydrophobic substrates was observed. Since formation of multilayers upon adsorption was also excluded, the difference in adsorption and flocculation behavior was related to the more compact conformation of hydrophobically associating derivatives in solution and at the interface. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3422–3429, 2006     

HDPE/LLDPE reactor blends with bimodal microstructures—part I: mechanical properties

Reactor blends of polyethylene/poly(ethylene-co-1-octene) resins with bimodal molecular weight and bimodal short chain branching distributions were synthesized in a two-step polymerization process. The compositions of these blends range from low molecular weight (LMW) homopolymer to high molecular weight (HMW) copolymer and, vice versa, HMW homopolymer to LMW copolymer. The physical properties of the blends were found to be consistent with the nature of the individual components. For the tensile properties, the stiffness decreases with increasing the fraction of the copolymer, regardless of the molecular weight of the homopolymer fraction. For these blends with bimodal microstructures, it was confirmed that the degree of crystallinity governs the stiffness of the polymer. However, the energy dampening properties of the polymers benefit from the presence of the copolymer. A balance of stiffness and toughness can be obtained by altering the composition of the blends. For some blends, the presence of HMW homopolymer can dominate the tensile properties, showing little variation in the stiffness with increased addition of copolymer. It was also demonstrated that the testing conditions and thermal treatment of the polymer greatly influence the resulting elastic and energy dampening properties. Depending on the desired application, annealing these polymers (especially very low density copolymers) not only increases the crystallinity and stiffness, but also changes the frequency response of the dynamic mechanical properties.     

Study of the sorption and acidic properties of MTW-type zeolite

The acidity of H-MTW-type zeolite has been investigated using infrared spectroscopy of adsorbed pyridine. Pore volume has been measured by nitrogen andn-hexane adsorption. The zeolite exhibits infrared signals at 3612 and 3580 cm^–1 tentatively attributed to bridging hydroxyl groups vibrating in the main channel and in the six-membered rings of the structure, respectively. Both hydroxyl groups possess high acid strength and are readily accessible to pyridine. H-MTW shows an-hexane cracking activity at 350°C comparable to that obtained with MFI and BEA-type materials with a product selectivity between medium and large pore structural types.     

吸附法脱除丁烯中仲丁醇

针对丁烯水合生产仲丁醇过程中,剩余丁烯含有质量分数为0.1%~2.0%的仲丁醇(SBA)而不能满足工业循环的要求,开发了吸附法脱除仲丁醇的技术。对吸附剂进行了筛选,结果表明,所研制的PUMS-01吸附剂有很大的吸附容量,将其应用在兰州炼油化工总厂甲乙酮装置的侧线放大试验中,能将原料中SBA的质量浓度降至100 mg/L以下,再生后的吸附剂吸附性能良好,且稳定。     

改性活性炭的表面特性及其对苯酚的吸附性能

研究了表面改性对活性炭吸附苯酚性能的影响。研究发现,硫酸氧化可增加活性炭表面酸性基团的含量,提高了活性炭的表面亲水性,降低pHPZC值,因而对吸附水中的苯酚的性能产生明显影响,降低了对苯酚的吸附。     

非常规汽油脱硫技术

水蒸气脱硫是一种以水代替氢的脱硫方法,降低脱硫成本显著。以酶代替传统加氢催化剂的生物脱硫技术是一个引人注目的课题。结合催化和精馏的催化精馏脱硫法,在选择脱硫的对象上,相对传统的催化脱硫更具优势。萃取脱硫是采用一些极性溶剂混合物脱除汽油馏分中的硫化物,须加入氧化助剂才有较好的脱硫效果,由此将导致大的辅助车间和有限脱硫效率。膜过程脱硫、声化学脱硫、等离子体和光脱硫都属于物理方法,环保意义很大。对于吸附脱硫,从流化催化裂化汽油中除硫完全,而汽油产率降低很少,辛烷值几乎没有损失,是一种有前途的脱硫方法。     

Effects of the sintering atmosphere on Nb-based dielectrics

The effects of a forming atmosphere on the stability, the sintering and the dielectric properties of Ba₅Nb₄O₁₅, BaNb₂O₆, ZnNb₂O₆ and Zn₃Nb₂O₈ ceramics were investigated, because of the primary importance of the sintering atmosphere in relation to copper sintering. These Nb-based materials were sintered in air and in Ar/H₂10%. Zn-containing samples are very sensitive to the reductive atmosphere. ZnO volatilises at 800–850 °C and the resulting compound does not exhibit the expected properties. BaNb₂O₆ and Ba₅Nb₄O₁₅ are more stable in term of relative weight loss. Nevertheless, the phase analysis reveals a modification of the BaNb₂O₆ phase, what induces the degradation of the dielectric property stability versus temperature. The properties of Ba₅Nb₄O₁₅ are not modified by a sintering in reductive atmosphere. A relative permittivity of 38.8, a permittivity temperature coefficient of −150 ppm °C⁻¹ and an insulating resistivity of 10^10.9 Ω cm were obtained for this latter.     

Compatibility of polysaccharide/maleic copolymer blends. IV. Thermal behavior of hydroxypropyl cellulose‐containing blends

The compatibility of the hydroxypropyl cellulose (HPC) with maleic acid–vinyl acetate copolymer in the solid state was studied by thermogravimetry, thermo‐optical analysis, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and optical microscopy. It was established that physical interactions are prevalent in blends with a high content of HPC, whereas chemical interactions predominate in blends with a medium and low content of HPC. By increasing the temperature, the thermochemical reactions are favored. Thermal properties are dependent on the mixing ratio of the components. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2585–2597, 2003