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1、国际会议口头报告ppt演讲内容准备模板The Draft of Academic Presentation国际会议的口头报告模板，每页ppt你需要讲什么东西需要分页详 细写，尽量口语化，如下是本人参加比利时会议的模板，供大家 参考。P1开场白：I am so honored to be with you to communicate academic questions and ideas.The t订e of my academic presentation is“The prep aration andcatalytic performance of porous silicananotu。

2、be functioned with heteroatoms ”I shall only take tenI will talk about theP2First of all, i wannatechnology, nanjing city,P3The content is listedP4minutes of your time.topic on the preparation introduce myself. I come china.as follows.of porous materials.from nanjing university ofAll our researches 。

3、are conducted by the academic thoughts. Generally speaking, we are committed to porous materials. In order to explore high- performance functionalized materials for Pilot experiments and scale-up production; we tune the structure, such as composition andmorphology step by step and optimize them furt。

4、her. Whats more, thepossible synthesis mechanisms are also investigated. Today, the presentation is based on the right-hand branch.P5It is known that mesoporous silica have excellent characters as the catalyst carrier, such as But due to lack of active sites, we have to introduce organic or inorgani。

5、c species as active sites. And the catalytic performance need to be further improvedP6As we know, the three factors including activity, scale and diffusion factor play decisive role in the catalysis, affecting the yield, selectivity, stability strongly. In our presentstion, we mainly focus on the in。

6、fluence of scale factor on the catalysis.P7Due to lack of active sites for mesoporous silica, two main methods (surface loading, modified framework) are widely reported， by which various organic or inorganic active sites can be immobilized on the surface or incorporated into the framework of mesopoo。

7、us silica. P8Though various morphologies of mesoporos silica were widely synthesized, the synthesis of the mesoporos silica, with three simultaneous characteristics including doped metal, mesoporous strueture and specific morphology, is always a challenge, which is rarely reported.In other words, fo。

8、r our case exploring a proper condition, at which the silicon and metal sources can simuItaneously hydrolyze, can ensure a desired material.P9Next, let s look at the synthetic steps Firstly, .Then, After that, .At last, we obta ined theproduc ts.PIOIn this work, by changing the synthesis conditions,。

9、 such as，and so on, the pure mesoporous silicawith different morphologies were synthesized, including nanosphere, nanorod, helix, capsule and nanotube. We will focus on the preparation and catalytic application of mesoporous silica with nanotube morphology.Pllthe SEM images of samples: Al, A2, A3 ar。

10、e shown in the figure. Itcan be see n that sample al is nano wire- like with len gth of about 2 卩 mand diameter of about lOOnm. When the amount of is 0. 04g, the morphology of sample A2 became to be short and thick rods and the size is about 1 卩 m in lengthand 400nm in diameter, respectively. With f。

11、urther increasing the amount of ，the sample A3 and A4 turned to be spherical morphology. It also can be seen that the diameters of samples A3 and A4 are substantially the same about450nm. However, the spherical morphology of A4 is more regular than that of A3. The XRD patterns showed four reflection。

12、 peaks attributed to (100), (110),(200) and (210), respectively, due to the hexagonal sructure.P12Then, we keep the same amount of , increasing the amount ofWe found that the length increased gradually. The XRD patterns also showedthe hexagonal sructure of samples Bl, B2, B3, B4P13Moreover, an addit。

13、ional proof of the hexagonal symmetry structure is given by TEM and the FT patt ern. The N adsorp ti on-desorp tion iso therms of the samples Bl, B2, B3, B4 exhibit a typical 2typeIV isotherm.According to the table of struetural parameters, we can find that the specific surface area and total pore v。

14、olume increase gradually, the thickness of wall decrease and there is no obvious change in diameter.P14Furthermore, the possible synthesis mechanism of the mesoporous silicananotube in dual templates system was proposed. We suggest that due toelectrostatic repulsion between positively charged ammoni。

15、um ions from hydrated ammonia molecules and hydrophilic groups of especially in ammonia (NH, 25wt %) solution, the high concentrated ammonium ions provide a crowded and 3 repulsive space to prevent the conjunction of molecules, leading to the formation of the rodlike micelles as template to form por。

16、e strueture instead of sphere-like ones. The role of cotemplate is suggested to tune the lengthof rod-like micelles by arranging itself along the axis of channel with+PE0 and PPO part immersed in the hydrophilic and the hydrophobic group of CTA respectively. As aresult, the mesoporous nanotube with 。

17、different length will be synthesized.However, the non-polar micelles are not affected by positively charged ammonium. When the amount of co-template increased further, the non-polar micelles tend to control the morphology of micelles which are sequentially from nanotube, short rod to sphere-like one。

18、s. It my be the reason that the nonpolar micelles would provide stronger attractive force than the electrostatic repulsion derived from the PEO block, ammonium ions and head group of , respectively.P15In order to investigate the influence of the morphology and structure of mesoporous silica on catal。

19、yticperformance, the samples with copper incorporated were synthesized.P16The figure shows the SEM and TEM images of samples al, a2, a3, from which we can see they represent incrementai length in the range of about 0 5, 1. 0 and 1.5 卩 m, and in sig ni fica nt cha nge indiameter around lOOnm. In XRD 。

20、patterns, there are also four reflection peaks for the samples with copper incorprated, respectively, which indicates the incorporation of the inorganic copper salt has no obvious effect on the hexagonal sructure and the ordered degree of pore strueture. Moreover, the trends in length and the diamet。

21、er of nanotube are illustrated.P17The N adsorp tio n-desorp tion iso therms of the samples al, a2, a3 exhibit a typical typeIV isotherm 2according to the IUPAC classification and no hysteresis loop at the relative pressure range of 0.2?p/p?0.4, implying the samples not only have ordered mesoporous s。

22、trueture but also the uniform 0pore size. Moreover, the pore diameters did not change significantly at different weight ratio of . . . / The most probable pore sizes of samples al, a2, a3 are determined to be 2. 71, 2. 50, 2. 44 nm, respectively. The struetural parameters are listed in following tab。

23、le.P18This table summarized the catalytic activity of coppermodified porous silica nanotube in the direct hydroxylation of benzene with HO as oxidant. The catalysts showed high catalytic activity， and 22direct proportional relationship between the benzene conversion and the length of the silica nano。

24、tube. Considering the similar copper content determined by ICP, the variations of catalytic activities were probably caused by different retention time of reagent in the nanotube with different lengths. P19It is Summary and Future ResearchThis part of research can be summed up from the following three aspects.Mophology control, Catalytic activity and Future research 看 this slide.P20 thanks。