彩色打印机特性化多元回归模型的研究

多元回归法是彩色打印机特性化普遍采用的方法,实验对影响多元回归精度的阶数、色空间选择、以及训练样本选取进行了研究.研究结果表明:(1)二、三、四阶的特性化精度分别在10.9±0.3、6.6±0.2、6.0±0.2个CIELAB色差单位;(2)回归模型采用RGB到CIELAB或CIEXYZ的预测精度基本相同,大概相差1个...     

广角镜头桶形畸变的二元二次多项式修正法

为了修正广角镜头的桶形畸变,提出了一种基于二元二次多项式的修正方法,阐述了其图像的像素坐标校正和像素灰度恢复方法。该方法首先用模板对广角镜头进行对准相对标定,然后用二元二次多项式拟合畸变图像与非畸变图像像素坐标之间的规律,最后把该方法应用于某广角镜头拍摄的图像,并采用最小二乘法对校正效果进行评价。结果表明:在不考虑视觉系统具体参数的情况下,该方法能够有效地对广角镜头桶形畸变进行修正。     

Digital computation of transient characteristics of an induction motor on switched supply

A novel method of computing the nonlinear differential equations relating to the transient behaviour of an induction motor using a polynomial series, is presented. The stator and rotor currents and the angle of rotation are expressed as polynomial series dependent on time. These are then substituted into the differential equations of the induction motor to compute the polynomial coefficients and, consequently, the transient quantities. Since the equations are nonlinear, the computations are carried out using the step-by-step method. The stator and rotor currents, speed and torque are calculated for acceleration and braking conditions. The results are compared both analytically and experimentally.     

Extensions of quantum enveloping algebras

In this paper, we define a class of extended quantum enveloping algebras U _q (f(K, J)) and some new Hopf algebras, which are certain extensions of quantum enveloping algebras by a Hopf algebra H. This construction generalizes some well-known extensions of quantum enveloping algebras by a Hopf algebra and provides a large of new noncommutative and noncocommutative Hopf algebras.     

Photoreactive fluorinated polyimide protected by a tetrahydropyranyl group (THP) based on photo-induced acidolysis

A polyimide (6F-THP) with a tetrahydropyranyl group (THP) in its side chain has been synthesized. The THP group exhibits a high acidolysis rate in this polymer's film. This rate was faster than that of a tertbutoxycarbonyl group (t-BOC), which has been previously reported [1]. Furthermore, the deprotected fluorinated polyimide (6FDA-AHHFP) became soluble in an aqueous base due to the presence of a hydroxyl group attached to the phenyl group of the diamine segment. The polyimide thus provides high performance as a photopolymer when used in conjunction with a photoacid generator after the post-exposure baking process (PEB). The photoacid generators used in this study were p-nitrobenzyl-9,10-dimethoxyanthoracene-2-sulfonate (NBAS) and diphenyliodonium-9,10-dimethoxyanthoracene-2-sulfonate (DIAS). The quantum yields of photodissociation and photoacid generation were also measured. The photoacid-generating quantum yields closely corresponded to the photosensitivities of the photoreactive polyimide system. It was confirmed that the THP group was easily deprotected even in the 6F-THP film with p-toluenesulfonic acid as a model acid catalyst. The activation energy of the THP deprotection reaction was determined to be 12.8 kcal/mol (19.5 kcal/mol in the case of t-BOC). The relationships between the THP deprotecting rate constant (k_d) and acid molecular size and between k_d and polyimide structure were further investigated.     

Recurrence formulas for molecular integrals over Laguerre Gaussian-type functions

Recurrence formulas for overlap, nuclear attraction, and electron-repulsion integrals over Laguerre Gaussian-type functions are presented. They have been derived using compact recurrence relations for homogeneous solid spherical harmonic operators but are rather lengthy as compared to those over Cartesian Gaussian-type functions. © 1998 John Wiley & Sons, Inc. Int J Quant Chem 66 : 273–279, 1998     

Pattern formation of polyimide by using photosensitive polybenzoxazole as a top layer

A versatile method for positive-type patterning of polyimide (PI) based on a two-layer photosensitive poly(benzoxazole) (PSPBO) and poly(amic acid) (PAA) film has been developed to provide a promising material in the field of microelectronics. This patterning system consisted of a pristine PAA thick bottom-layer and a poly(o-hydroxy amide) (PHA) thin top layer with 9,9-bis[4-(tert-butoxycarbonyl-methyloxy)phenyl]fluorene (TBMPF) as a dissolution inhibitor, and (5-propylsulfonyloxyimino-5H-thiophene-2-ylidene)-(2-methylphenyl)-acetonitrile (PTMA) as a photoacid generator (PAG). The PHA and PAA were prepared from 4,4′-(hexafluoroisopropylidene)-bis(o-aminophenol) and 4,4′-oxybis(benzoic acid) derivatives, and 3,3′,4,4′-biphenyltetracarboxylic dianhydride and 4,4′-oxydianiline, respectively, in N,N-dimethylacetamide. This two-layer system based on PHA (150-nm thickness) and PAA (1.5-μm thickness) showed high sensitivity of 35 mJ/cm² and high contrast of 10.3 when exposed to a 365 nm line (i-line), post-baked at 100 °C for 2 min, and developed in a 2.38 wt.% tetramethylammonium hydroxide aqueous solution/5 wt.% iso-propanol at 25 °C. A clear positive image of a 4-μm line-and-space pattern was printed on a film which was exposed to 100 mJ/cm² of i-line by a contact-printing mode and fully converted to the corresponding PBO/PI pattern upon heating at 350 °C, confirmed by FT-IR spectroscopy. This two-layer system could be applied to the patterning of various PAAs.     

Vapor pressure,speciation, and chemical activities in highly concentrated sodium borate solutions at 277 and 317°C

The system H₂O-B₂O₃-Na₂O has been studied experimentally at 277 and 317°C. The activities of water and boric acid have been determined at mole ratios Na/B from 0 to 1.5, and total dissolved solids 3 to 80 weight percent. The activity of boric acid has been fitted to within experimental error using a speciation model with eight complex species. This model is consistent with the model previously published by Mesmer et al. The electrolyte properties of the liquid are modeled using the Pitzer-Simonson model of very concentrated electrolyte solutions. The calculated values of water activity agree with experiment, and the activity of NaOH and pOH have also been calculated. The potassium borate system also was briefly studied at 317°C, and is adequately described by a model with five complex species. The potassium borate liquid is more alkaline at K/B= 1 than a sodium borate liquid at the same mole ratio, but pOH in the two systems is the same at lower mole ratios.