涤纶复合丝（POY＋DTY）的研发

DTY和POY网络复合丝是以聚酯直纺生产的两种不同规格的POY丝为原料,通过对加弹机进行适当改造,利用不同的加工路线,使一股POY丝经过加捻后形成DTY,再与另一股POY丝网络合股形成包芯复合丝.该复合丝利用POY丝和DTY丝的收缩差异和染色差异等不同风格特性,使得布面形成一种具有雪花状的色丁效果.该复合丝属于差别化纤维,是国家鼓励发展的项目,它具有优良的吸湿排汗性能和弹性保暖性能,是保暖内衣的首选面料,市场前景广阔.     

A new space-vector-modulated control for a unidirectionalthree-phase switch-mode rectifier

A unidirectional three-phase switch-mode rectifier that delivers sinusoidal input currents in phase with the corresponding input phase voltages is proposed and analyzed in this paper. In the proposed topology, three AC switches are placed before the bridge rectifier and, respectively, across two power lines. A simple control scheme combing space-vector modulation and hysteresis current control is presented. Sinusoidal input line currents are observed in experimental results     

Performance evaluation of a multichannel transceiver system forADSL and VHDSL services

The authors study the performance of a multichannel modulation method for asymmetric digital subscriber lines (ADSLs) and very high-speed digital subscriber lines (VHDSLs). In the ADSL case, over all unloaded North American subscriber lines in the test set, a unidirectional 1.536 Mb/s data rate service from the end office to the customer premises is possible on a single twisted pair at an error rate of 10^-7 with at least a 6 dB margin used coded multichannel modulation with sufficient transmit power. In the VHDSL case, data rates in excess of 100 Mb/s can be transmitted reliably, at an error rate of 10^-7, using uncoded multichannel modulation on a single twisted pair over a distance ⩽150 ft with a sufficiently high sampling rate (≈24 MHz) and transmit power. It is shown that a cost-effective multichannel transceiver design suggested for high-speed digital subscriber line (HDSL) service will also work well for ADSL and VHDSL services with only minimal modifications     

Synthesis,characterization, and redox and electrochromic behaviors of poly(3-n-octyloxythiophene)

Poly(3-n-octyloxythiophene), a conjugated polymer, which possessed solubility in common organic solvents, was synthesized by electrochemical polymerization in the presence of lithium perchlorate as the supporting electrolyte and sodium dodecyl sulfate as the surfactant in an aqueous medium. Characterizations of the intermediate, monomer, and polymer were performed by NMR spectroscopy, Fourier transform infrared spectroscopy, ultraviolet–visible spectroscopy, and gel permeation chromatography. The process of electrochemical polymerization and the electrochemical redox behaviors were investigated by cyclic voltammetry and the potentiostatic method. A poly(3-n-octyloxythiophene) film that was deposited on a platinum electrode was found to exhibit electrochromic behaviors, and it switched electrochemically between blue–green oxidized and dark red reduced states. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Isobaric vapor–liquid equilibria for mixtures of tetrahydrofuran, 2-propanol, and 2,2,4-trimethylpentane at 101.3 kPa

Vapor–liquid equilibrium (VLE) at 101.3 kPa have been determined for a ternary system (tetrahydofuran + 2-propanol + 2,2,4-trimethylpentane) and its constituent binary systems (tetrahydrofuran + 2-propanol, tetrahydrofuran + 2,2,4-trimethylpentane, and 2-propanol + 2,2,4-trimethylpentane). The activity coefficients of liquid mixtures were calculated from the modified Raoult's law. Thermodynamic consistency tests were performed for all VLE data. The VLE data of the binary mixtures and ternary mixtures were correlated using the Margules, Wilson, NRTL, and UNIQUAC activity-coefficient models. The models with their best-fitted interaction parameters of the binary systems were used to predict the ternary vapor–liquid equilibrium. All VLE data are also used to calculate the reduced excess molar Gibbs free energy g^E/RT and the deviations in the boiling point ΔT. The calculated quantities of g^E/RT and ΔT were fitted to variable-degree polynomials in terms of liquid composition.     

Stability of Mixtoxantrone Hydrochloride in Solution

A stability-indicating reversed-phase high performance liquid chromatographic method was developed for the detection of mitoxantrone HC1 and its degradation products under accelerated degradation conditions. The degradation kinetics of mitoxantrone HC1 in aqueous solution over a pH range of 1.18 to 7.20 and its stability in propylene glycol-or polyethylene glycol 400-based solutions were investigated. The observed rate constants were shown to follow apparent first-order kinetics in all cases. The pH-rate profile shows that maximum stability of mitoxantrone HC1 was obtained at pH 4.01. No general acid or base catalysis from acetate or phosphate buffer species was observed. The catalysis rate constants on the protonated mitoxantrone imposed by hydrogen ion water and hydroxy ion were determined to be 3.72 × 10 min^-1 5.64 × 10-min^-1 and 1.108 × 10^-2min^-1, respectively. The degradation rate constants of mitoxantrone affected by different ionic strength systems. Irradiation with 254 nm UV light at 25±0.5°C was found when canpared with the light-protected controls. Incorporation of nonaqueous propylene glycol or polyethylene glycol in the pH 4.01 mitoxantrone solution shows an increase in its stability at 502±0.5°C.     

环丙基砜衍生物的合成研究

在温和的碱性条件下,以TosMIC为砜源,对2-酰基-1-氯环丙烷羧酸酯的区域进行选择性加成,直接合成具有潜在生物活性的环丙基砜类化合物,产率可高达85％,非对映选择性可超过20:1.研究结果首次证明了TosMIC与缺电子环丙烯的亲核加成反应.     

工业废渣磷石膏用作充填材料的研究

研制了以工业废渣磷石膏为基材的充填材料.改性后磷石膏的耐水性大大增强,抗压强度≥0.79 MPa、渗透系数≤1×10-5cm.s-1,并且具有合适的C、Φ值.     

间二甲苯-磷酸-水三元体系的液-液相平衡

实验测定了不同温度下,间二甲苯-水二元体系和间二甲苯-磷酸-水三元体系的液-液相平衡数据。研究了磷酸中的杂质Fe~(3+)、Al~(3+)和Mg~(2+)对间二甲苯-磷酸-水三元体系相平衡的影响,以及杂质在两相中的分配情况。研究结果对共沸精馏浓缩磷酸提供了必要的理论依据和基础数据。     

Tar sand extractions with microemulsions: I-the dissolution of light hydrocarbons by microemulsions using 2-butoxyethanol and diethylmethylamine as cosurfactants

For oil sand extractions with microemulsions it is important to disperse large quantities of light hydrocarbons in an aqueous medium. Fundamental studies on the properties of 2-butoxyethanol (BE) and diethylmethylamine (Et₂McN) in water suggest that these two liquids could be more effective cosurfactants than the usual alcohols used for this purpose. The phase diagrams of microemulsions using BE and Et₂MeN as cosurfactants, combined with typical ionic and non-ionic surfactants and typical aliphatic and aromatic hydrocarbons, were therefore investigated and compared with microemulsions based on n-butanol. Although the phase diagrams depend significantly on the nature of the surfactant and of the oil, the monophasic region generally increases with the cosurfactant in the order n-butanol < Et₂McN < BE. With the active mixture BE-cetyltrimethylammonium bromide, temperature has little effect on the phase diagram and NaCl generally destabilizes the microemulsion.