Formation of isocyanic acid during the reaction of mixtures of NO, CO and H2 over supported platinum catalysts

On-line infrared spectroscopy has been used to show that isocyanic acid, HNCO, is a substantial primary product of the reaction between NO, CO and H₂ over a Pt/SiO₂ catalyst. At 230°C it accounts for more than 40% of the CO converted. No isocyanic acid is seen when Al₂O₃ is placed downstream of Pt/SiO₂, or when using a Pt/Al₂O₃ catalyst under the same conditions, due to rapid hydrolysis of HNCO on the alumina. Isocyanic acid may exist as a trace intermediate in automobile catalytic converters during their warm-up phase but it is unlikely to emerge from the pore system of aluminabased catalysts.     

应用线性矩阵不等式解决时滞系统控制问题

介绍了应用线性矩阵不等式（LMI）解决一类时滞系统H∞控制问题,给出了基于Lyapunov第二法的H∞稳定条件,通过求解锥补线性化问题,得到相应的控制器,使得闭环系统稳定且满足H∞性能指标.并通过实例给出了仿真结果.     

Graft copolymerization of 2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid onto carboxymethylcellulose (sodium salt) by H2O2/Fe+2 redox pair

The effect of the reaction conditions on the grafting parameters during grafting of 2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid onto sodium carboxymethylcellulose using H₂O₂/Fe⁺² redox pair are studied at 30°C. The grafting ratio, add on, and conversion initially increase with the H₂O₂ concentration in the range of (10.0–15.0) × 10^?2 mol dm^?3. Thereafter, these parameters decrease with the H₂O₂ concentration. The grafting ratio, add on, and conversion increase when increasing the ferrous ion concentration from (0.5 to 4.0) × 10^?2 mol dm^?3 and decrease with a further increase in the concentration. It is observed that the grafting ratio and add on increase with the monomer concentration, whereas the conversion decrease. The hydrogen ions seem to be facilitating the grafting reaction up to a certain concentration and after this concentration seem to be retarding the process. The grafting ratio, add on, and conversion decrease with the sodium carboxymethylcellulose concentration. When increasing the time period from 60 to 90 min, the grafting parameters increase but decrease thereafter. Similarly, when increasing the temperature from 25 to 30°C, the grafting parameters increase and decrease thereafter. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4819–4825, 2006     

Gasoline composition determined by H NMR spectroscopy

A fast and simple ¹H NMR spectroscopic method was developed for the concentration measurement of aromatic, olefinic and aliphatic fractions in gasoline samples. Simultaneously, individual components such as benzene, methyl tert-butyl ether and several dienes could be determined. The method relies on only a few, well-established assumptions about the molecular compositions and is therefore applicable to a broad range of gasolines. It is well suited for laboratories with high sample throughput since measurement time is short and all concentrations are determined within one NMR experiment. The method was applied to commercial gasolines and samples used in European round robin tests. Comparisons of NMR and round robin test results showed excellent agreement.     

采用读卡机芯片FM1715SL设计的RFID读卡机

根据车辆管理系统对身份识别需求,提出基于国产芯片的RFID读卡机方案。数据接口设计为ISO14443TypeB的设备,在满足安全保密前提下,很好地兼顾了使用方便和高效便捷,大规模的车载应用验证了该方案的可靠性。     

Modification of catalytic performances due to the co-feeding of hydrogen or carbon dioxide in the partial oxidation of methane over a NiO/γ-Al2O3 catalyst

The influence of the addition of 1–10 vol.% of hydrogen or carbon dioxide to the feed during the partial oxidation of methane was studied over a NiO/γ-Al₂O₃ catalyst. The addition of H₂ decreases the conversion and syngas selectivity. This decrease of performance seems to be related to a higher reduction of the catalyst due to the H₂ co-feeding. The addition of CO₂ also appears unfavorable to the production of hydrogen but increases the CO yield. A combination of the dry reforming and the reverse water gas shift reactions is suggested to explain the observed modifications in the product yields.     

1H nuclear magnetic resonance study of polyurethane prepolymers from toluene diisocyanate and polypropylene glycol

Polyurethane prepolymers prepared from toluene 2,4‐diisocyanate, toluene 2,6‐diisocyanate, and polypropylene glycol with a ratio between the isocyanate and hydroxyl groups equal to 2 were analyzed by ¹H nuclear magnetic resonance (NMR) spectroscopy in acetone‐d₆. Different temperatures and concentrations were used. Toluene 2,4‐dimethylurethane and toluene 2,6‐dimethylurethane were synthesized and used as model compounds to assign prepolymers signals. Measurements of spin–lattice relaxation time T₁ by “inversion recovery” experiments were carried out on toluene 2,4‐diisocyanate, toluene 2,6‐diisocyanate, toluene 2,4‐dimethylurethane, toluene 2,6‐dimethylurethane, and polyurethane prepolymers. Differences in T₁ times were used to interpret prepolymers spectra, by means of the strong observed effect on protons due to the presence of adjacent isocyanate groups. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 347–357, 2003     

Hydrogenolysis of alkanes and olefin polymerization on the silica-supported zirconium hydrides: A comparative DFT study

The model reactions of ethylene polymerization and hydrogenolysis of linear alkanes (propane, n-butane, and n-pentane) on the silica-supported zirconium hydrides (Si–O)₃Zr^IVH, (Si–O)₂Zr^IVH₂, and (Si–O)₂Zr^IIIH were studied using the DFT approach. Catalytic processes under study were shown to occur involving different surface hydrides. The ethylene polymerization was found to proceed at comparable rates on the zirconium monohydrides, (Si–O)₃ZrH, and dihydrides, (Si–O)₂ZrH₂. Cleavage of linear alkanes on the monohydrides (Si–O)₃ZrH is thermodynamically unfavorable; however, the dihydrides (Si–O)₂ZrH₂ can act as catalysts of the process under mild conditions. Hydrides of the trivalent zirconium, (Si–O)₂Zr^IIIH, can also contribute to the hydrogenolysis reaction. A feature of all the systems studied is low regioselectivity of the corresponding processes.     

方法研究在X公司机加工车间的应用

为改善X公司机加工车间不合理的生产方式,通过现场观察和咨询,对其血液分析仪不规范的装配流程运用"5W1H"提问技术并结合"ECRS"原则进行分析、改善,制定出标准的装配流程;针对同步带齿轮的加工过程中时间利用不科学的问题,运用人机操作分析法进行分析,同时改进齿轮的设计,最终使得人机加工周程时间节约了25 s,齿轮的增值时间利用率由原来的43 %增加到59 %,这些活动为该公司进行的生产管理改善提供了依据.     

基于塞班智能手机的视频监控设计与实现

智能手机的发展推动了视频监控方式的改变。该文以Symbian S60作为客户端软件设计的开发平台,利用RTP的API接口来接收服务器端发送的流媒体数据,对接收到的数据先进行NALU重组,然后送给ffmpeg解码器,最后采用直接屏幕访问来播放视频。