氮在含氧Mo(100)面上的吸附与反应

 用HREELS, AES, LEED和TDS考察了氮在含氧Mo(100)上的吸附和热脱附. 120 K下氮在含氧Mo(100)上吸附时存在着N—N伸缩振动频率2150和1600 cm-1, 分别对应于线式(γ态)和侧位(α态)两种分子吸附态. 升温引起γ态氮的脱附和α态氮的解离. 其中γ态氮的脱附峰温位于155 K, 遵循一级脱附动力学; 由α态解离生成的N原子占据Mo(100)的四重空位(即β态), 并在高于1?150 K的温度重新化合形成氮而脱附. 120 K时,氮的吸附是无序的; 吸附了氮的表面经1100 K退火后生成了有序的c(2×2)-N表面结构.     

Crystal and Molecular Structure of 1-Phenoxy(α-methyl)acetyl-2-diethylamino-3-phenyl-1,3,2-diazaphospholidin-4-one-2-sulfide

1　INTRODUCTIONAsherbicides,thearyloxycarboxylicacidssuchas2,4-D(2,4-Dichlorophenoxyaceticacid)etc.havenotbeenusedwidelysince1970sbecauseoftheircausingenvi-ronmentalpollutionandinjuriestothecrops.Studiesonthenewtypeofherbicideshavebeendevelopinginrecentyears.Itwasreportedrecentlythatthederivativesofdiazaphospholidinoneorthecorrespondingthionespossessinterestingherbicidalactiv-ity[1～3].Itwasalsoknownthat1,4,2-diazaphospholidine-5-thione-2-oxideshasgoodselectiveherbicidalactivity[4,5],but…     

K3C60单晶膜的同步辐射光电子谱研究

在C₆₀单晶(111)解理面上制备出厚度约30 nm的K₃C₆₀单晶膜.利用同步辐射光源,在低温下(约150K)测量了样品法向发射的角分辨光电子谱.观察到K₃C₆₀导带和价带明显的色散.导带的光电子谱峰可清晰分辨出4个子峰,这些子峰的最大色散超过0.5eV,并且色散曲线与K₃C₆₀的一维无序晶体结构模型下的能带理论基本吻合,只是子带间隔差异较大.     

Determination and Temperature Dependence of Plateau Modulus for Polymerization of Propylene to Isotactic Polypropylene with Ultra-high Molecular Weight under Catalysis of Ziegler-Natta Catalyst

The viscoelastic behavior of isotactic polypropylene with ultra-high molecular weight (UHPPH) and broad molecular weight distribution(MWD), produced in the presence of Ziegler-Natta catalyst, was investigated by means of oscillatory rheometry at 180 and 200 ℃, whose loss modulus(G") plots at 180 and 200 ℃versus the natural logarithm of angular frequency(ω) present a pronounced maximum at 34.35 and 69.21 rad/s, respectively, and do not show a maximum peak at 0. 01-100 rad/s for Ziegler-Natta catalyzing ethylenepropylene random copolymerization (PPR) with a conventional molecular weight and broad MWD. The fact indicates that the high molecular weight is responsible for a maximum peak of G"(ω) vs. lnω curves for UHPPH. This makes it possible to determine the plateau modulus (G0N) of UHPPH from a certain experimental temperature G"(ω) curve directly. For UHPPH, the G0N determined to be 4. 28×105 and 3. 62×105 Pa at 180and 200 ℃, respectively, decreases with the increase of temperature and is independent of the molecular weight, which directly confirms reputation theoretical prediction that the G0N has no relation to the molecular weight.     

CO在Sm/Rh(100)模型表面上的吸附与反应

应用AES,LEED,XPS和TDS研究了Rh(100)上Sm膜和Sm/Rh表面合金以及CO在这两类模型表面的吸附与反应.室温下Sm在Rh(100)上的生长遵从SK模式,Sm膜经900K高温退火后可形成有序表面合金.在室温制备的Sm膜/Rh(100)表面上,室温下CO在Sm上的吸附改变了表面结构,生成SmOx和表面碳.随着Sm覆盖度的增加,低温脱附峰(α-CO)面积迅速下降,且峰温向高温方向位移;表明Sm的空间位阻和电子效应同时起作用.在Sm/Rh合金表面上,CO在约590K出现新的脱附峰,可归属为受Sm电正性修饰的Rh原子上的CO脱附峰     

Crystal Structure of Ethyl 4-benzoyl-1a,2,3,4-tetrahydro-3-methyl-1a-(4-methylphenyl)-1H-azirino〔1,2-a〕〔1,5〕 benzodiazepine-1-carboxylate(C_(28)H_(28)N_2O_3)

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Synthesis and Crystal Structure of a Mixed Cu - Cd Bim etallic Com plex ｛〔 Cu Cd(pba)( H_2 O)_3〕·2 H_2 O｝ _n

１　ＩＮＴＲＯＤＵＣＴＩＯＮＨｅｔｅｒｏｍｅｔａｌｐｏｌｙｎｕｃｌｅａｒｃｏｍｐｌｅｘｅｓｈａｖｅｂｅｅｎｔｈｅｓｕｂｊｅｃｔｏｆｍａｎｙｒｅｃｅｎｔｓｔｕｄｉｅｓｔｏｅｌｕｃｉｄａｔｅｔｈｅｍｅｃｈａｎｉｓｍｏｆｓｐｉｎｃｏｕｐｌｉｎｇｂｅｔｗｅｅｎｔｈｅｍｅｔａｌｉｏｎｓ〔１,２〕,ｍｉｍｉｃｋｉｎｇｔｈｅａｃｔｉｖｅｓｉｔｅｏｆｓｏｍｅｍｅｔａｌｅｎｚｙｍｅｓｃｏｎｔａｉｎｉｎｇｄｉｓｓｉｍｉｌａｒｍｅｔａｌｉｏｎｓ,ｓｕｃｈａｓｃｙｔｏｃｈｒｏｍｅｏｘｉｄａｓｅａｎｄｓｕｐｅｒｏｘｉ…     

^15NO与Mo（100）—c（2＊2）N表面相互作用的HREELS和TDS研究

利用高分辨子能量人谱和热脱附谱,研究了在Ｍｏ（１００）－ｃ（２＊２）Ｎ表面上的吸附态及其随温度的变化,１２０Ｋ时,在Ｍｏ（１００）－ｃ（２＊２）Ｎ表面低暴露的＾１５ＮＯ发生解度和分子吸附,解离生成的＾１５Ｎ在１２３０Ｋ与另一＾１５Ｎ原子或氮化钼中的＾１４Ｎ原子并合,脱附,在升温时大部分分子吸附的＾１５ＮＯ发生解离和反应,解离生成的＾１５Ｎ原子与另一＾１５Ｎ原子生成＾１５Ｎ２而脱附,与表面残存＾１５     

苯酚在热氧化法制备的SnO2/Ti 电极上的电氧化研究

A SnO₂/Ti electrode prepared by thermal oxidation was used as the anode for galvanostatic electrolysis in acidic solution containing phenol, the time-dependances of phenol concentration,chemical oxygen demand in solution(COD)and instantaneous current efficiency were determined during electrolysis.The results show that with the SnO₂/Ti anode instead of Pt,the COD significantly decreases at the same charge passage, and average current efficiency of oxidation increases by three times The mechanism for phenol oxidation at two electrodes was discussed.