基于小波基优化和动态比特分配的数字音频压缩编码方案

提出了一种新颖的基于自适应小波基优化选择和心理声学模型相结合的数字音频信号的透明质量编码方法，保证固定失真水平上使每帧信号的变换系数的动态分配的比特数最少，并且利用动态码本的方法来消除音频信号的统计冗余，进一步压缩比特率，对于抽样率为４４．１ｋＨｚ每样值用１６比特线性码表示的光盘单声道音乐信号可以压缩到６４ｋＢＰＳ左右。     

Gas-phase selective oxidation of toluene on TiO2–sepiolite supported vanadium oxides: Influence of vanadium loading on conversion and product selectivities

Gas-phase selective oxidation of toluene has been carried out on vanadium oxide systems (5–20 wt.% of V₂O₅, equivalent to 0.4–1.7 theoretical monolayers) supported on TiO₂–sepiolite (with titania loading around the theoretical monolayer, 12 wt.%) and on sepiolite. A study has been made on both the influence of vanadia loading and of the support on the catalytic behaviour of the supported vanadium systems. The reducibility by H₂ TPR was also studied as well as the acid and basic/redox sites from the results of conversion of the 2-propanol test reaction of the solids. Benzaldehyde, benzoic acid and several coupling products were the main ones detected, attaining over 50% selectivity towards the benzaldehyde and benzoic acid products at a total conversion around 10%. The activity and selectivity to the selective products exhibited by vanadium systems supported on mixed support were superior to those exhibited by the systems supported on sepiolite and increased notably in both series with the increase in vanadium loading. The best catalytic behaviour exhibited by the vanadium systems supported on mixed support, which also exhibited the highest density of sites capable of being reduced (as well as their reducibility) and of those responsible for propanone formation, could be attributed not only to the different balance of the vanadia species existing in the two supports (monomeric + oligomeric/polymeric), but also to such other factors as the nature of the support and, concretely, its chemical composition.     

异丁烷与丁烯在炭化树脂负载PW_(12)催化剂上的烷基化

探讨了炭化树脂负载杂多酸PW1 2 催化剂制备的适宜条件 ,反应工艺条件对催化剂催化异丁烷与丁烯烷基化反应及产物分布的影响 ,分析了催化剂具有较高活性的原因 ,进行了催化剂稳定性实验。并与其它类固体酸催化剂进行了对比。     

糠醛临氢脱羰催化剂的研制开发

提出了一种可应用于糠醛临氢脱羰的新型催化剂—Pt催化剂。通过实验确定了其最佳载体和助剂及反应条件 ,开发出一种以Pt为主的脱羰催化剂 ,并进行了 5 0 0h的寿命实验 ,其呋喃产率高于 80 %,优于已知Pd催化剂 ,现已投入工业应用。     

NdCl_3·nTBP/MgCl_2-AlR_3催化体系合成丁二烯橡胶

探讨了以NdCl_3的磷酸三丁酯(TBP)溶液为主催化剂、烷基铝为助催化剂、MgCl_2为载体组成的Ziegler-Natta型催化体系引发丁二烯(Bd)聚合的某些规律。用AlEt_3作助催化剂,聚合物的顺1,4-结构含量仅为57％,反1,4-结构含量为42％;而以Al(i-Bu)_3作助催化剂,聚合物的顺1,4-结构含量为88％,反1,4-结构含量为11％。各种陈化体系中,以NdCl_3·nTBP/MgCl_2-Al(i-Bu)_3-Ip三元体系的催化活性最高,当Nd/Bd(摩尔比)为7×10~(-5)时,单体转化率达80％。低温聚合可获得高顺式、高分子量聚合物。     

On the specific reactivity of platinum segregated layers on Pt80X20 (111) (X= Ni,Co, Fe) alloys

The influence of alloying of Pt with 20 at.% of Ni, Co and Fe has been studied in the hydrogenation of 1,3 butadiene. Iron induces the more important modifications, with both higher activity and selectivity. The results are discussed in terms of the surface segregation, the local order in surface and the electronic properties measured by photoemission of core levels.     

A survey of CSCW systems

Over the last decade, computer supported cooperative work (CSCW) has emerged as an identifiable research area that focuses on the role of the computer in group work. CSCW is a generic term which combines the understanding of the nature of group working with the enabling technologies of computer networking, systems support and applications. The paper examines the classes of system which have emerged to support cooperative working. A framework for characterising and describing CSCW systems is presented and four major classes of cooperative system identified. Each of these classes of cooperative system are examined highlighting their general characteristics and applicability to CSCW.     

HRP-12型负载杂多酸催化剂的失活原因及预防措施

采用XRD、NMR、IR、MS等手段对长链烷基苯合成中失活负载型杂多酸催化剂进行了表征,结果表明,催化剂的失活主要是由于表面结焦引起的,原料中的双烯、烷基芳烃杂质以及反应生成的副产物重烷基苯是引起催化剂结焦的主要原因,对原料进行脱双烯和脱芳烃精制、提高苯烯比以及用苯洗涤催化剂等措施能够有效抑制催化剂的失活。     

Influence of Pt particle size on catalytic combustion of xylenes on carbon aerogel-supported Pt catalysts

Pt catalysts supported on a carbon aerogel with different Pt particle sizes were studied in the combustion of o-xylene and m-xylene. Results found show that the activity of the catalysts increased with larger Pt particle size. In addition, the catalysts were activated during consecutive combustion runs and during time on stream. This activation depends on the Pt particle size and type of xylene isomer. Activation was due to the increase in Pt particle size during reaction. The lower activity of catalysts with smaller Pt particle size was due to the stronger PtO bonds formed during xylene combustion by the smaller Pt particles.     

The effect of support morphology on the reaction of oxidative dehydrogenation of ethane to ethylene at short contact times

The oxidative dehydrogenation of ethane is carried out in short contact time reactors over Pt and LaMnO₃ based catalysts supported on a large number of different ceramic substrates (45, 60 and 80 ppi foam monoliths and 200, 400, 600, 900 and 1200 cpsi honeycomb monoliths). Experimental results, obtained under the same conditions at varying the C₂H₆/O₂ ratio, showed that the highest performance in terms of ethylene selectivity and yield is always attained on LaMnO₃ catalysts. Furthermore, the results are significantly influenced by the morphology and cell density of the support, with 45 and 60 ppi foams and 400 and 600 cpsi honeycombs giving the best performance. The experimental results are explained by means of geometrical and fluid dynamic considerations on the support, and by means of a 2D mathematical model, which clearly indicates an optimal intermediate cell density for maximising ethylene selectivity and yield.