空间晶体生长流体效应的实验研究和理论分析

在空间晶体生长实时观察装置上，利用溶液中形成的铌酸钾微晶作示踪粒子，首次在空间高温氧化物熔液内，实时观察和记录了空间表面和力对流效应。利用测量的结果计算了熔体内空间表面张力对流的速度场，并与地面表面张力对流的速度场进行了对比，理论计算与实验结果基本吻合。探讨了空间均匀分布铌酸钾微晶的形成机理。结果表明：表面张务对流在空间晶体生长过程中起主要作用，是形成均匀分布胞状晶体的主要机理。     

Effect of Residual Surface Stress on the Strenght Distribution of Brittle Materials

The introduction of residual surface stresses into a material can change the strength distribution simply due to variability in the stress intensity factor of surface cracks. This variability arises from the distribution in surface (critical) crack lengths. A fracture mechanics approach was used to determine the influence of surface compression on the average strength and the standard deviation of the strength distribution. The strengths of the stress-free samples were assumed to fit a twoparameter Weibull distribution, and the increases in strength resulting from the surface compression were determined using fracture mechanics. It was determined from the analysis that the standard deviation/average strength ratio (coefficient of variation) initially increases, passes through a maximum, and ultimately reaches a plateau value below the initial value, as one increases the depth of surface compression. The maximum increase in the strength scatter occurs when the depth of the surface compression is approximately equal to the characteristic crack size. These changes were found to be dependent on the magnitude of the surface stress, as well as the characteristic strength, Weibull modulus, and fracture toughness of the stress-free material.     

Fluorinated acrylic polymers: Surface properties and XPS investigations

A series of polymers based on methylmethacrylate, butylacrylate, and ω‐perfluorooctylalkylacrylate were prepared by radical polymerization. By changing both the length of the hydrocarbon spacer, between the fluorinated chain and the ester function of the fluorinated monomer, and its concentration, the surface properties of the resulting terpolymers were greatly influenced. Polymers containing small amounts of fluorinated comonomer units had considerably reduced surface energies compared to the copolymer poly (methylmethacrylate‐co‐butylacrylate) taken as reference. The outermost surface composition has been investigated by the XPS technique, confirming the strong fluorine enrichment. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 821–827, 2006     

Interphases in the Adhesive Bonding of Fluoropolymers

Strong and durable adhesive bonds may be made between polytetrafluoroethylene (PTFE) and either cyanoacrylate (CA) or epoxy adhesives, if the PTFE surface is modified by the use of a “primer” such as triphenylphosphine (TPP) or diaminodiphenylmethane (DDM). The primer mixes with the PTFE surface, and the modified surface is then capable of forming an interphase, tens to hundreds of nanometers thick, where interpenetration of the adhesive and adherend occurs. Using CA adhesives, PTFE/CA/PTFE block compression shear bond strength (ASTM D4501-85) of over 10 MPa can be achieved, with failure occurring cohesively. Initial work with epoxy adhesives indicates that the use of DDM primer gives adhesive bonds comparable in strength with those produced by modification of the fluoropolymer surface by sodium naphthalenide.     

高锰酸盐复合药剂预氧化处理微污染水

通过生产性试验考察了高锰酸盐复合药剂预氧化处理微污染水的除污染效能.结果表明,高锰酸盐复合药剂预氧化强化了对浊度、有机物及铁、锰等污染物质的去除,并且与常规工艺相比能较好地控制出厂水三卤甲烷的生成量.     

气相法白炭黑表面处理的新方法

在辅助处理剂的存在下，六甲基二硅氮烷（HMDZ）可以很好地对气相法白炭黑进行表面处理。处理后的气相法白炭黑适合于制作双组分室温硫化（RTV-2）硅橡胶；讨论了气相法白炭黑与HMDZ的配比，反应温度，反应时间等对RTV-2硅橡胶性能的影响。最佳反应条件为：100份气相法白炭黑用17份HMDZ处理。反应温度120℃，反应时间60min以上，采用处理后的白炭黑填充的RTV硅橡胶具有优良的机械性能和操作性能。     

响应面法优化酶催化酯交换反应研究

为了利用植物油生产可再生的绿色能源——生物柴油,文章利用Novo435固定化脂肪酶,在无有机溶剂存在下催化菜籽油与甲醇酯交换合成生物柴油。利用响应面实验设计和分析方法对菜籽油的酯交换反应条件进行优化,得到了最佳工艺条件:醇油摩尔比1.5∶1,反应温度52℃,搅拌转速200 r/min,脂肪酶与油脂的质量比为10%,反应时间10 h,在此工艺条件下油脂的酯交换率达到48%(理论为50%)。理论甲醇量分3批加入,反应36 h后菜籽油的总酯交换率达到95%(理论酯交换率为100%)。每批试验后利用有机溶剂对脂肪酶进行清洗,然后继续反应,连续使用10个批次,油脂的酯交换率基本未变。     

The meaning of surface area and porosity measurements of clays and pillared clays

Pillared clays (PC) generally present textural complexity, geometrical constraints and possible chemical heterogeneity by pillaring. As far as surface area and porosity measurements by physical adsorption of nitrogen are concerned, this overall complexity introduces interpretation difficulties. We consider two aspects of this problem in pillared clays.The textural complexity stems from the distribution of charge density, from the deformation of the host layers and from their entanglement. The microtexture is controlled by the wet preparation chemistry, to a large extent by the drying method as examplified by the titanium pillared montmorillonites.The geometrical constraints arise from the fact that the interlamellar space of the PC is (so far) microporous or just mesoporous. The small distance between the layers, of the order of one or a few molecular diameters, is therefore expected to perturb the arrangement of the pore filling molecules. The molecular confinement is a major source of underestimation of the total pore volume in the interlamellar space. It makes the surface area determination difficult and of little physical significance. Probably microporosity values are more valuable criterion of pillaring as shown in the titanium pillared samples.In addition to these two aspects, one has also to consider a possible chemical heterogeneity arising from the simultaneous presence of pillars, exchangeable ions and precipitated species. This can lead to a complex behaviour of surface area and microporosity as examplified by the mixed aluminium-iron pillared laponites.     

Root growth and phosphorus and potassium uptake by two corn genotypes in the field

In a field study P and K uptake by two corn (Zea mays L.) genotypes which differed in root growth was investigated. The effect of differences in root growth on P and K uptake was assessed using a mechanistic-mathematical model which describes nutrient uptake by growing plant roots in soil. Nitrogen was applied at 0 and 227 kg ha^–1 to Pioneer 3732 and B73xMo17 corn grown on Raub silt loam (fine-silty, mixed, mesic Aquic Argiudoll) and at 227 kg N ha^–1 to these two genotypes on Chalmers silt loam (finesilty, mixed, mesic, Typic Haplaquoll). Root growth and P and K uptake by the two corn genotypes was measured 31, 47, 75 and 91 d after planting on the Raub and 31, 47, 61 and 75 d after planting on the Chalmers soil.Root growth and P and K uptake by B73xMo17 was greater than that of Pioneer 3732 on N-fertilized Raub soil. On Chalmers soil the difference in root growth between the two genotypes resulted in an increase in K but not P uptake. The higher soil P level of the Chalmers appears to have offset possible differences in P uptake due to root size. There were no differences between the two genotypes in either the percentage of roots with root hairs, or the density or length of root hairs. Phosphorus and K uptake calculated with the simulation models for both corn genotypes on both soils over each of three growth periods agreed with observed P (Y = 0.68X + 1.71; r = 0.944^**) and K (Y = 0.88X + 15.52; r = 0.928^**) uptake. Differences in P and K uptake between B73xMo17 and Pioneer 3732 resulted primarily from the difference in root growth in the topsoil. A high correlation was found between root surface area and P (r = 0.893^**) and K (r = 0.928^**) uptake by both corn genotypes on both the soils.Journal paper No. 10,316 Purdue Univ. Agric. Exp. Stn., W. Lafayette, In 47906. Contribution from the Dep. of Agron. This paper was supported in part by a grant from the Tennessee Valley Authority.     

Silver catalysts supported over activated carbons for the selective oxidation of CO in excess hydrogen: effects of different treatments on the supports

Commercial activated carbon (AC) was used as a support either in its original form or after various modifications, giving diverse textural and surface chemical characteristics. The changes of these properties were monitored by N₂ adsorption–desorption isotherms, temperature programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). Ag catalysts were prepared over the AC supports by a conventional wet impregnation method. The catalytic performances of supported Ag/AC catalysts in the selective oxidation of CO in excess H₂ were tested. The results indicate the textural and surface chemical characteristics are responsible for the different catalytic performances.