一种对称非均匀细分曲面算法

为了得到能更好应用于CAD系统的细分曲面造型方法,提出一种基于B-样条的对称非均匀细分算法,其中的思想和均匀Lane-Riesenfeld节点插入算法相似。基于B-样条的节点插入算法,以Blossoming为工具,计算出细分后的新控制顶点。细分后得到的极限曲面由张量积样条曲面组成,在奇异点达到2C连续。与传统的细分曲面算法相比,该细分曲面算法具有良好的局部支撑性,大大降低了算法的复杂度,而且该算法是对称的,不用考虑定向问题。     

Cutting force estimation in sculptured surface milling

Cutting force milling models developed up to now are mostly used for planar milling using end-mills. Only a reduced number of models applying ball-end mills have been developed. Furthermore these models usually only consider horizontal surface machining, even though the main application of ball-end mills is sculptured surface machining. This article proposes a model that is able to estimate the cutting forces in inclined surfaces machined both up-milling and down-milling. For this purpose a semi-mechanistic model has been developed that calculates the cutting forces based on a set of coefficients which depend on the material, the tool, the cutting conditions, the machining direction and the slope of the surface.A coordinate transformation has been included in order to consider the slope milling case with different cutting directions.The model has been tested on two materials, an aluminum alloy Al7075-T6 and a 52 HRC tool steel AISI H13. Validation tests have been carried out on inclined planes using different slopes and different machining directions.The results provide errors below 10% in most of the cases and both the value and shape of the predicted forces adjust the measured cutting force.     

Surface photografting polymerization of vinyl acetate,maleic anhydride,and their charge‐transfer complex. VI. Charge‐transfer complex (2)

The photografting copolymerization of a low‐density polyethylene/vinyl acetate (VAC)–maleic anhydride (MAH) binary monomer system was studied from the perspective of dynamics. The total conversion percentage (CP) and grafting conversion percentage (CG) were measured by gravimetry. On the basis of plots of CP and CG as functions of the polymerization time, the total polymerization rate (RP) and grafting polymerization rate (RG) were calculated. In addition, the apparent activation energy (E_a) and the reaction orders of the photografting polymerization under different reaction conditions, such as the total monomer concentration and the concentration of benzophenone (BP), were determined also. The results showed that, in comparison with the photografting polymerization of the two single monomers (VAC and MAH), RP and RG noticeably increased for the VAC–MAH binary monomer system. When the total monomer concentration was kept at 4M, the apparent E_a's of the three photografting polymerization systems were as follows: for VAC ([MAH]/[VAC] = 0/4), E_a's for the total polymerization and grafting polymerization were 41.00 and 43.90 kJ/mol, respectively; for MAH ([MAH]/[VAC] = 4/0, E_a's were 39.65 and 43.23 kJ/mol, respectively; and for the VAC–MAH binary monomer system, E_a's were 34.35 and 40.32 kJ/mol, respectively. These results suggested that the polymerization of the binary system occurred more readily than the other two. The reaction orders of RP with respect to the total monomer concentration of the monomers and the concentration of BP were 1.34 and 0.81, respectively. According to these investigations, it could be inferred that in the binary monomer system, both the free monomers and charge‐transfer complex took part in the polymerization; to the termination of the propagating chains, two possible pathways, unimolecular termination and bimolecular termination, coexisted in this binary monomer system. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 910–915, 2005     

180°矩形弯管流场的实验测量和数值模拟

对180°矩形弯管内的湍流流场用智能型五孔球探针进行了测量，同时采用FLUENT 6.2对其进行数值模拟。流场测量和数值模拟结果表明：180°矩形弯管由于流体旋转产生的离心力导致了弯管内压力分布的变化，使弯管内切向速度发生变化。切向速度在流体开始旋转0°~60°区间内侧的速度增大、压力减小，外侧的速度降低、压力增大；当转过60°截面后，外侧的速度增大、压力减小，内侧的速度降低、压力增大。     

On the Predominant Electron-Donicity of Polar Solid Surfaces

The reasons for the predominant electron-donicity of almost all solid polar surfaces and its implications are discussed in this paper. By contact angle or interfacial tension measurements, the electron-accepting as well as the electron-donating properties of polar liquids can be ascertained, through the interplay between their energies of adhesion and cohesion. For the solid-liquid interface, direct interfacial tension measurements are not possible, but indirectly, solid/liquid interfacial tensions of polar systems can be obtained by contact angle measurement. However, as the energy of cohesion of a solid does not influence the contact angle formed by a liquid drop placed upon its surface, one can only measure the solid surface'ks residual polar property, manifested by the energy of adhesion between solid and liquid. This residual polar property is of necessity the dominant component; in most cases this turns out to be its electron donicity. When, by means of contact angle measurements with polar liquids, both electron-accepting and electron-donating potentials are found on a polar solid, it is most likely still partly covered with a polar liquid: usually water. The amount of residual water of hydration of a polar solid follows from its polar (Lewis acid-base) surface tension component (γ^AB). The degree of orientation of the residual water of hydration on a polar solid can be expressed by the ratio of the electron-donating to electron-accepting potentials (γ^⊖/γ^⊕), measured on the hydrated surface.     

Surface hydrolysis of filaments based on poly(trimethylene terephthalate) spun at high spinning speeds

The surface alkaline hydrolysis of fibers made from poly(trimethylene terephthalate) (PTT) was studied after extruding the polymer at high spinning speeds from 2000 to 6000 m/min and heat setting in the range of temperatures from 100 to 180°C. Fiber weight loss increased with an increasing heat‐setting temperature but it was also dependent on the spinning speed. Some of the partially hydrolyzed fibers had a well‐developed, hydrophilic surface, and pore size in the range of 0.69 to 1.20 μm. The optimum reaction and morphological conditions for increasing porosity in PTT fibers depends on spinning speed and heat‐setting temperature. A temperature of 180°C is the upper limit for heat‐setting PTT filaments but seems to be the most effective for making porous fibers. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1724–1730, 2004     

Surface morphology and nodule formation mechanism of cellulose acetate membranes by atomic force microscopy

By the use of atomic force microscopy (AFM), formation mechanism of nodular structure in cellulose acetate membranes was systematically investigated. Elementary factors affecting the nodule formation were delineated on the basis of both kinetic and thermodynamic considerations. It was shown that (1) the exact nature of nodular structure is thermodynamic equilibrium glassy state; nodular structure will vanish in the rubbery state; (2) the thermodynamic factor affecting nodule formation is the membrane formation temperature; with the membrane formation temperature decreasing, more chain segments are able to form nodular structures; (3) nodule formation is dependent on the segment rearrangement; variation of the solvent environment is the major kinetic factor affecting the segment rearrangement and nodule formation. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1328–1335, 2003     

Evaluation of some of the properties of plasma treated wool fabric

Low temperature plasma (LTP) treatment was applied to wool fabric with the use of a nonpolymerizing gas, namely oxygen. Properties of the LTP‐treated samples including low stress mechanical behavior, air permeability, and thermal characteristics were evaluated in this study. Kawabata evaluation system fabric (KES‐F) was employed to determine the tensile, shearing, bending, and compression strength properties and surface roughness of the specimens. The changes in these properties are believed to be closely related to the interfiber and interyarn frictional force induced by the LTP. The decrease in the air permeability of the LTP‐treated wool fabric was found to be probably because of the plasma action effect on increasing the fabric thickness and a change in fabric surface morphology, which was confirmed by scanning electron microscopy micrographs. The change in the thermal properties of the LTP‐treated wool fabric was in good agreement with the earlier findings and can be attributed to the amount of air trapped between the yarns and fibers. This study suggested that the LTP treatment can influence the final properties of the wool fabric, and also provide information for developing LTP‐treated wool fabric for industrial use. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5958–5964, 2006