TRI.BE(트라이비),

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问题一、东方神起《tri

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（米奇)从来没有在他的基因基里和我结合起来，把黎凡纳的人和扎比兰的人联系起来，他知道金戈加（英雄)南义哲博吉的事，如果他把盖吉的事搞砸了，他就知道吕文基的事，但是在朱胜利的事上，苏仲哈的事*(全)穆金卡思梅佩尼穆丽莉李易斋和葛鲁在李嘉丽的李嘉丽的李嘉丽的李嘉丽的李嘉丽是李嘉丽的李嘉丽(米奇麦克斯)中演唱蔡菊的《李嘉仪》李安的李嘉丽的《李嘉仪》李嘉丽的李嘉丽的《李嘉丽的李嘉丽》李嘉丽的《李嘉丽的李嘉丽》李嘉丽的《李嘉丽的李嘉丽》穆嘎当有苏嘎和乐虎奈林奴卡姆吉和宁洱别苏嘎吉帕古丁阿品桑色甘依耒您能告诉我吗和最大值你得到了力量~巴鲁扎啤苏嘎伊宁嗨米尔内内内内内内比哈吉迈沮鹄德音嘎泽金艾力德利尔比JIU亚伊(xiah) 我不知道你为什么讨厌这一刻，因为林子密的萨朗林迪在米埃布达古哈吉安你为什么要告诉我重复*(夏赫)萨朗哈宁萨朗雷迪努否认ba ki ki bi bo yi ji a ni(英雄)伊sei伊三卡茨伊in格德卢卡德嘎丹格马莱JIU(boa) 南和凯是金烈在阿迪阿木在伊斯吗和盖别伊乐迪嘎宁德普顾漫伊达宁根格德素娥(说唱)(特拉斯)有一天，尼加被李甲的林芒哲尼纳马甲纳马甲纳马甲纳梅歌土木工程师的李甲布吉马甲纳梅朗一个我从一个流动我们要的流动我们要的流动（全部)我得到了流动， 现在我在土里长大吴丽和艺伎慕汝菊顾自故滑稽我说不(你知道米奇)伊哲乌文林姬娜安妮你在你巴古苏嘎伊达谷米在德伊和苏格里尔麦在《卡基卡基》( u-know max) 木嘎当有苏总代理人和尼格布勒乃林奴卡姆吉和宁洱别苏嘎吉帕古丁阿品桑色甘依耒德宁卡恐惧苏妮和您必须遵守《全国人大常委会关于维护互联网安全的决定》及中华人民共和国其他有关法律法规忠哈给吉基吉居苏伊给曼乐迪亚伊阿久安阿久安阿久安阿久安阿久安阿久安阿久安阿久安阿久安阿久安阿久安阿久安阿久安阿久安12|什么事

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问题二、moontri可以组成什么单词？

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月光戒指吴亚玲吴亚玲：监视器喂？喂[m(r)]年复一年[医]名.1740年，慕克玲；张伯伦医生，云娥；你好吗，阿曼苏丹国；（朱庇隆（伊朗伊斯兰共和国))何如，云斯；（你好)阿云哥；阿宽；绿筠；阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉阿吉五个。苏梅！苏梅；你好吗（阿悦

播或电话）；监控（无线电或电视传输信号）[ 复数 monitors 第三人称单数 monitors 现在分词 monitoring 过去式 monitored 过去分词 monitored ]短语system monitor 系统监视器 ; 系统监控 ; 系统监控器 ; [计] 系统监督程序LCD Monitor 液晶显示器 ; 液晶监视器 ; 显示器 ; 液晶显示屏baby monitor 婴儿监视器 ; 婴儿监控器 ; 本产品词组短语monitor system 监控系统；执行系统computer monitor 电脑显示器remote monitor 遥控监视器；远距离监控装置video monitor 显示器；视频监视器pressure monitor 压力监测器双语例句Your doctor will monitor your blood pressure. 你的医生会监测你的血压。《柯林斯英汉双解大词典》The heart monitor shows low levels of consciousness. 心脏监控器显示低意识水平。《柯林斯英汉双解大词典》Officials had not been allowed to monitor the voting. 官员们未曾获许监控选举。《柯林斯英汉双解大词典》

推荐问题五、高分请朋友帮忙检索文献翻译的英文原文【时间紧迫，好必追加】

,: PROCESS FOR THE DIRECT SYNTHESIS OF TRIALKOXYSILANE Abstract: The Direct Synthesis of trialkoxysilane is carried out by concting the Direct Synthesis reaction of silicon and alcohol, optionally in solvent, in the presence of a catalytically effective amount of Direct Synthesis catalyst and an effective catalyst- promoting amount of Direct Synthesis catalyst promoter, said promoter being an organic or inorganic compound possessing at least one phosphorus-oxygen bond. 具体请自己查找PROCESS FOR THE DIRECT SYNTHESIS OF TRIALKOXYSILANECROSS REFERENCE TO RELATED APPLICATIONThis application claims priority to U.S. provisional application Serial No. 60/716,728, filed September 13, 2005, the entire contents of which are incorporated by reference herein.FIELD OF THE INVENTIONThis invention relates to the Direct Synthesis of trialkoxysilane by the catalyzed reaction of silicon with alcohol. In particular, the Direct Synthesis process of the present invention employs organic and inorganic phosphorus compounds such as copper phosphates, trialkyl phosphates and dialkyl phosphites to increase the reaction rate, promote selectivity to trialkoxysilane, control formation of tetraalkoxysilane and improve reaction stability in batchwise, semi-continuous and continuous operations.BACKGROUND OF THE INVENTIONTrialkoxysilanes, especially trimethoxysilane, triethoxysilane and tri(isopropoxy)silane, are used in the proction of silane coupling agents. One method of synthesis of trialkoxysilanes is directly from silicon and an alcohol in the presence of copper or a copper compound. This method is known variously in the art as the Direct Synthesis, the Direct Reaction, the Direct Process or the Rochow Reaction. For trialkoxysilanes, it is most conveniently performed in slurry reactors.In a slurry reactor for the Direct Synthesis of trialkoxysilane, catalytically- activated silicon particles are maintained in suspension in a thermally stable, high boiling solvent and are made to react with an alcohol at an elevated temperature. The proct stream exiting the reaction zone comprises a mixture of unreacted alcohol, trialkoxysilane, tetraalkoxysilane, alkyldialkoxysilane, alkyltrialkoxysilane and condensed silicates. Trialkoxysilane is usually the desired proct. However, there are instances in which the tetraalkoxysilanes and alkyldialkoxysilanes are also sought and methods and processes which increase the formation of these co-procts are known in the art. The trialkoxysilane proct and desired co-procts are typically recovered by distillation.The rate of the Direct Synthesis of a trialkoxysilane is the temporal consumption of the raw materials (that is, alcohol or silicon), or the temporal formation of procts (trialkoxysilane,optionally including by-procts). Familiar units are weight percent silicon conversion per hour, or kilograms proct per kilogram silicon per hour.Selectivity is the preference for the trialkoxysilane under the reaction conditions. It is expressed herein as the gravimetric ratio trialkoxysilane/tetraalkoxysilane. Alternatively, selectivity can be expressed as mole percentage, i.e., 100 moles trialkoxysilane/molar sum of all silicon-containing procts.Stability is the maintenance of desirable rate and selectivity until all raw materials are consumed, or consumed beyond a preset criterion. The progress of the Direct Synthesis can be monitored by determining proct composition and/or reaction rate as a function of time or silicon conversion. In general, the reaction profile shows an initial period (referred to as the inction period) of increasing rate and increasing trialkoxysilane concentration in the reaction mixture, after which the reaction settles into a steady state. In this state, the composition of the reaction mixture remains approximately constant. A period of declining rate and decreasing trialkoxysilane content in the proct mixture follows the steady state.It is generally accepted that the actual catalysts in the Direct Synthesis of silicon are the copper-silicon alloys or inter,llics and solid solutions formed by the diffusion of copper into silicon, or by the reaction of copper compounds with silicon. Thus, the copper-containing raw materials effective in activating silicon for the Direct Synthesis with alcohols are all catalyst precursors and will be referred to as such. A wide variety of such precursors has been disclosed in the prior art.U.S. Patent No. 3,641,077 discloses the slurry-phase preparation of trialkoxysilanes by directly reacting copper-silicon mass, suspended in silicone oil, with alcohol at 250 – 3000C. The copper-silicon mass contains about 10 weight percent copper and is prepared by heating copper and silicon above 1000°C in a furnace in a stream of hydrogen gas.U.S. Patent No. 3,775,457 discloses the use of cuprous chloride and HF or HCl in the slurry-phase Direct Synthesis of silicon and alcohols. Ammonium chloride is used to restore waning reactivity.Japanese Patent Publication 55-28929 (1980) acknowledges that activation of silicon with CuCl does not always lead to desirable rate and selectivity. The patent teaches treatment of CuCl with nitriles, naphthalenes, biphenyls and anthracenes prior to its use in the Direct Synthesis.Japanese Patent Publication 55-2641 (1980) discloses the use of cyclic ethers such as dibenzo-18-crown-6 to improve the reaction rate and the yield of trialkoxysilane.U.S. Patent No. 5,362,897 discloses the use of specially prepared “wet process” CuCl, in preference to commercial “dry process” CuCl, and silicon containing 0.30 – 0.37 weight percent aluminum to obtain high reaction rates and silicon conversions. “Wet process” CuCl is defined (column 2, lines 51 – 54) as that “prepared through the steps of crystallization and separation and drying. Dry process CuCl is prepared from ,llic copper and chlorine gas (column 2, lines 62 – 65).U.S. Patent No. 5,527,937 discloses a slurry-phase process for the Direct Synthesis of triethoxysilane wherein CuCl is the copper source, tri- and tetra- toluenes and/or their alkyl-substituted derivatives are the solvents and dimethylsilicone oils are employed as antifoaming agents. The method by which CuCl was prepared is not disclosed.Japanese Patent Application 3-354055 (1991) discloses the use of copper alkoxides, with or without copper chlorides, as catalyst precursors for the Direct Synthesis of trialkoxysilanes.Japanese Patent Application 6-306083 (1994) discloses improved selectivity and rate for the Direct Synthesis of trialkoxysilanes are realized when a an organosulfur compound such as a mercaptan, disulfide, thioheterocyclic (e.g.,thiophene) or and Cu(II) thio-complex (e.g., bis(4-methylthiophenol)copper(II) is present in the reaction slurry catalyzed with a copper alkoxide. The patent discloses that appropriate quantities of these compounds can be added to the reaction when selectivity has decreased. Alternatively, the compounds can be introced at the outset of the reaction or continuously in the alcohol feed.Japanese Patent Application 10-168084 (1998) and Japanese Patent Application 10 – 338696 (1998) both disclose cupric oxide having a water content of less than 3000 parts per million and an average particle size of 0.1 – 50 micrometers as the catalyst precursor in a process for manufacturing trialkoxysilanes.U.S. Patent No. 6,727,375 and Standke et al., Silicon for the Chemical Instry VI, pp. 225 – 231 (2002), disclose processes for the …..

六、（日语歌词我有）《枪神tri gun》的ED也是主题曲《风は未来に吹く》的罗马音 谢谢

风は未来に吹く ka ze ha mi ra i ni fu ku青い空の下で 风は未来に吹くa o i so ra no shi ta de ka ze ha mi ra i ni fu ku 太阳の日差しを 抱きしめるようにta i yo u no hi za shi wo da ki shi me ru yo u niただ流されるだけ 足迹だけを残してta da na ga sa re ru da ke a shi a to da ke wo no ko shi te 頬をなでる空気と ねころぶ草があればho ho wo na de ru ku u ki to ne ko ro bu ku sa ga a re ba 他に何もいらない 満ち足りた笑颜でho ka ni na ni mo i ra na i mi chi ta ri ta e ga o de 果てしなく続く 明日を见つめ眠る ha te shi na ku tsu zu ku a shi ta wo mi tsu me ne mu ru La La La … 波音がきこえる 心をくすぐる na mi o to ga ki ko e ru ko ko ro wo ku su gu ru雨の滴みたいに 気ままにあてなく a me no shi zu ku mi ta i ni ki ma ma ni a te na ku静かに夕日が すべてを见届け shi zu ka ni yu u hi ga su be te wo mi to do ke远い海に沈む 口づけするように to o i u mi ni shi zu mu ku chi zu ke su ru yo u ni 果てしなく続く 明日の梦に流れる ha te shi na ku tsu zu ku a shi ta no yu me ni na ga re ru La La La … Sound Life So 1つ目の夜に いずこから小石が世界に落ちる So hi to tsu me no yo ru ni i zu ko ka ra ko i shi ga se ka i ni o chi ruSo 2つ目の夜に 小石の子が手を取りワルツを描く So fu ta tsu me no yo ru ni ko i shi no ko ga te wo to ri wa ru tsu wo e ga kuSo 3つ目の夜に ワルツの子は世界面にウェーブ(wave)を打つ So miittsu me no yo ru ni wa ru tsu no ko ha se kai men ni vo e bu wo u tsu So 4つ目の夜に 波の子は岸辺にしぶきを上げる So yottsu me no yo ru ni na mi no ko ha ki shi be ni shi bu ke wo a ge ruSo 5つ目の夜に そのかけら几度も世界面をたたくSo i tsu tsu me no yo ru ni so no ka ke ra i ku do mo se ka i men wo ta ta ku So 6つ目の夜に その合図に旅人は集い合うSo muttsu me no yo ru ni so no a i zu ni ta bi bi to ha a tsu do i a u So 7つ目の夜に 重さのなく船は空间へと走る So na na tsu me no yo ru ni ka sa no na ku fu ne ha ku u kan he to ha shi ru So 8つ目の朝に いずこからの歌が耳へと届くSo yattsu me no a sa ni i zu ko ka ra no u ta ga mi mi he to to do ku さあ 新しい空に全てを记した组曲が响く sa a a ta ra shi i so ra ni su be te wo shi ru shi ta ku mi kyo ku ga hi bi kuSound Life AKIMA & NEOS – Sound Life ～TRIGUN～ IN 作词:Nakazawa Kenji 作曲/编曲:Akima Tsuneo So 1つ目の夜に So hi to tsu me no yo ru ni いずこから小石が世界に落ちる i zu ko ka ra ko i shi ga se ka i ni o chi ruSo 2つ目の夜に So fu ta tsu me no yo ru ni ko i shi no ko ga te wo to ri wa ru tsu wo e ga ku 小石の子が手を取りワルツを描く ko i shi no ko ga te wo to ri wa ru tsu wo e ga kuSo 3つ目の夜に So miittsu me no yo ru niワルツの子は世界面にウエーブを打つ wa ru tsu no ko ha se kai men ni vo e bu wo u tsuSo 4つ目の夜に So yottsu me no yo ru ni na mi no ko ha ki shi be ni shi bu ke wo a ge ru波の子は岸辺にしぶきを上げる na mi no ko ha ki shi be ni shi bu ke wo a ge ruSo 5つ目の夜に So i tsu tsu me no yo ru ni so no ka ke ra i ku do mo se ka i men wo ta ta kuそのかけら几度も世界面をたたく so no ka ke ra i ku do mo se ka i men wo ta ta kuSo 6つ目の夜にSo muttsu me no yo ru ni その合図に旅人は集い合う so no a i zu ni ta bi bi to ha a tsu do i a uSo 7つ目の夜にSo na na tsu me no yo ru ni 重さのない船は空间(そら)へと走る ka sa no na ku fu ne ha ku u kan he to ha shi ruSo 8つ目の朝に So yattsu me no a sa ni いずこからの歌が耳へと届くi zu ko ka ra no u ta ga mi mi he to to do ku さあ 新しい空に全てを记した组曲が响くsa a a ta ra shi i so ra ni su be te wo shi ru shi ta ku mi kyo ku ga hi bi ku