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981.
Chin-Ping Yang Yoshiyuki Oishi Masa-Aki Kakimoto Yoshio Imai 《Journal of polymer science. Part A, Polymer chemistry》1989,27(12):3895-3901
Aromatic polyamides (aramids) having pendant t-butyl group were synthesized by the direct polycondensation of 5-t-butylisophthalic acid with various aromatic diamines in N-methyl-2-pyrrolidone (NMP) using triphenyl phosphite and pyridine as condensing agents. The aramids having inherent viscosities of 0.6–2.4 dL/g were obtained in quantitative yields. These polymers were readily soluble in various solvents such as NMP,N,N-dimethylacetamide, dimethyl sulfoxide, and pyridine, and gave transparent, tough and flexible films by casting from the NMP solutions. The aramids had glass transition temperatures between 250 and 330°C, and started to lose weight around 350°C, with 10% weight loss being recorded at about 450°C in air. 相似文献
982.
Shiow-Ching Chen Meei-Yun Shiue M.-H. Yang 《Analytical and bioanalytical chemistry》1997,357(8):1192-1197
A method is proposed which involves sample pretreatment followed by electrothermal atomic absorption spectrometry (ETAAS)
for determination of cadmium in human urine. A microwave digestion system was devised to accommodate double-closed vessels
for simultaneous digestion of batches of up to 24 urine samples in about 20 min. After digestion, matrix substances which
might interfere were removed using silica-immobilized 8-hydroxyquinoline (I-8HOQ) columns. The analyte adsorbed on the column
was then eluted with dilute nitric acid solution and determined by ETAAS using a fast temperature program. Neither ashing
steps in the furnace heating program nor use of matrix modifiers was necessary. The accuracy, precision, limit of detection,
and sample throughput of the method were evaluated. With meticulous control of systematic errors which may be introduced in
the pretreatment procedures, the present method can serve as a reference technique for the analysis of Cd in urine samples.
Received: 29 July 1996/Revised: 30 September 1996/Accepted: 13 October 1996 相似文献
983.
Shiow-Ching Chen Meei-Yun Shiue M.-H. Yang 《Fresenius' Journal of Analytical Chemistry》1997,357(8):1192-1197
A method is proposed which involves sample pretreatment followed by electrothermal atomic absorption spectrometry (ETAAS)
for determination of cadmium in human urine. A microwave digestion system was devised to accommodate double-closed vessels
for simultaneous digestion of batches of up to 24 urine samples in about 20 min. After digestion, matrix substances which
might interfere were removed using silica-immobilized 8-hydroxyquinoline (I-8HOQ) columns. The analyte adsorbed on the column
was then eluted with dilute nitric acid solution and determined by ETAAS using a fast temperature program. Neither ashing
steps in the furnace heating program nor use of matrix modifiers was necessary. The accuracy, precision, limit of detection,
and sample throughput of the method were evaluated. With meticulous control of systematic errors which may be introduced in
the pretreatment procedures, the present method can serve as a reference technique for the analysis of Cd in urine samples.
Received: 29 July 1996/Revised: 30 September 1996/Accepted: 13 October 1996 相似文献
984.
A method has been described for the direct determinations of trace cadmium using derivative atom trapping flame atomic absorption spectrometry with an improved water-cooled stainless steel trapping equipment. The characteristic concentration (gave a derivative absorbance of 0.0044) and detection limit (3sigma) of cadmium were 0.028 and 0.02 ng ml(-1) when collecting for a 1 min, respectively, which were 992 and 145-fold better than those of the conventional flame atomic absorption spectrometry. The detection limit and sensitivity of the proposed method for a 2 min collection time were 1 and 2 orders of magnitude higher than those of conventional flame atomic absorption spectrometry. The present method was applied to the determinations of cadmium in water samples with a recovery range of 91 approximately 111% and a relative standard deviation of 4.7 approximately 5.6%. 相似文献
985.
The photo‐initiated cationic polymerization (PCP) of epoxides using diaryliodonium salt photoacid generators (PAGs) bearing alkyl groups and anions was investigated. The properties and reactivities of a series of iodonium salts containing various cations and anions were compared in the context of a PCP reaction. The products from the decomposition of the cations of these salts were analyzed using gas chromatography‐mass spectrometry (GC‐MS) spectra. The relationship between the molecular structure of the salts and their reaction mechanism in the PCP reaction was investigated. Based on the results of the investigation, it was concluded that the structures of the cations and anions of theiodonium salts affect the PCP reaction rate, which was controlled by the products from the diaryliodonium salts. As part of an additional investigation, the diaryliodonium salts‐epoxide materials were applied to 254 nm‐photo‐patterning. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
986.
LBL分子沉积法制备葡萄糖氧化酶电极 总被引:1,自引:0,他引:1
采用以静电力为主的逐层分子交替沉积技术制备葡萄糖氧化酶(GOD)电极.通过带有正电荷的聚二甲基二烯丙基铵盐酸盐(PDDA)和带有负电荷的GOD交替沉积在修饰有3-巯基-1-丙基磺酸钠(MPS)的金电极表面.以甲酸二茂铁为电子媒介体,用循环伏安法检测GOD电极对葡萄糖的响应.结果表明,当GOD电极组装层数小于4时,电流响应随着层数的增加而增大,超过4层时电流响应减小.其中4层GOD修饰电极的线性范围为0.55~6.63 mmol•L-1,当pH为7.0时,响应最大.同时电极的检测重现性能良好,相对标准偏差为2.4%. 相似文献
987.
Kai Yang Xuan Zhang Enqin Fu Jingui Qin Minoru Kinoshita 《Journal of solid state chemistry》2004,177(11):4300-4304
Two new intercalation compounds were prepared by the reactions of Ni(II) cyclopolyamine complex cations with a preintercalate Mn1−xPS3K2x(H2O)y, respectively, through “ion exchange” process. Their structures were characterized by elemental analysis, X-ray powder diffraction and infrared spectroscopy. The lattice spacing increased 0.567 and 1.093 nm with respect to the pristine MnPS3. Ferrimagnetism of the intercalates was confirmed by SQUID experiment with Tc at 40 and 33 K, respectively. 相似文献
988.
Wang X Yu JC Yip HY Wu L Wong PK Lai SY 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(10):2997-3004
A novel metal/semiconductor nanocomposite with catalytic and photocatalytic functions has been prepared. The new material consists of highly dispersed platinum (Pt) nanoparticles embedded in a cubic mesoporous nanocrystalline anatase (meso-nc-TiO2) thin film. The porous thin film possesses a narrow pore-size distribution and a large surface area. The diameter of the Pt cluster can be controlled to below 5 nm, and the high dispersion of these clusters gives rise to catalytic activity for the oxidation of carbon monoxide, an important reaction for automobile exhaust treatment. This novel ordered mesoporous Pt/TiO2 nanoarchitecture is also a promising photochemical material, as demonstrated by the photo-driven killing of Micrococcus lylae cells on the film. 相似文献
989.
Patterned langmuir-blodgett films of monodisperse nanoparticles of iron oxide using soft lithography 总被引:7,自引:0,他引:7
Langmuir-Blodgett (LB) films of monodisperse iron oxide nanoparticles have been successfully deposited onto patterned poly(dimethylsiloxane) surfaces. These patterned LB films of iron oxide nanoparticles were transferred onto solid substrates using micro contact printing. 相似文献
990.
QuanliZhu JianYang JiaxinWang ShengfuJi HanqingWang 《天然气化学杂志》2003,12(1):23-30
The performance of uspported and unsupported molybdenum carbide for the partial oxidation of methane (POM) to syngas was investgated.An evaluation of the catalysts indicates that bulk molybdenum carbied has a higher methane conversion during the initial stage but a lower selectivity to CO and H2/CO ratio in the products.The rapid deactivation of the catalyst is also a significant problem.However,the supported molybdenum carbide catalyst shows a much higher methane conversion,increased selectivity and significantly improved catalytic stability.The characterization by XRD and BET specific area measurements depict an improved dispersion of molybdenum carbide when using alumina as a carrier.The bulk or the supported molybdenum carbide exists in the β-Mo2C phase,while it is transformed into molybdenum dioxide postcatalysis which is an improtant cause of molybdenum carbide deactivation. 相似文献