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If one has a feeling that Waley found what he needed to find——a wryness,adelicacy,a languor,that seems to imbue Genji and Yuan Mei,Sei Shonagon ,andMonkey,even the imperial commissioner Lin Tse-hsu---onecannot cavil and can immediately find other works thatnegate any simple genera1ization.

假如有谁觉得,韦利所发现的是他要发现的东西,这些东西就是看来浸润于源氏(大约指《源氏物语》。——译者)、袁枚、清少纳言和孙悟空,甚至是钦差大臣林则徐这些人和作品人物之中的谐谑、雅致和散淡,假如谁有这种感觉,这倒也没有甚么好说的。不过,人们还可以立即发现其他一些作品,让人无法再对韦利进行简单的归类。

Dealcoholization temperature markedly influences the surface area and porosity of the resultant MAO-supports. When the support was pretreated at lower or higher temperature, the corresponding MAO-support shows very low surface area;2.XRD and IR analyses indicate that MAO has reacted with the residual ethanol in the supports, which is an important manner to get MAO fixed on the carrier. Morever, XPS analyse indicates that MAO can also be coordinated with MgCl_2, which is another way to get MAO fixed on the support;3.ICP and EDX analyses indicate that dealcoholization temperature not only determined the element content on the solid catalyst, but also influences the element distribution on the carrier;4.The activities of the supported phenoxy-imine catalysts and the properties of resultant polymers are strongly dependent on the dealcoholization temperature. The support (MSP-5) obtained by treating MgCl_2·2.56C_2H_5OH at 160℃for 4 h, then modified by MAO is very effective for immobilizing complex 3, the resultant solid catalyst (MSPC-5) shows very high activity in ethylene polymerization, and its kinetics of polymerization is stable during the reaction process. Finally, PEs with spherical morphology and high bulk density (over 0.35g/ml) were obtained, without reactor fouling;5.In this work, polymerization conditions such as alkylaluminums, Al/Zr ratio, temperature and H_2 had a pronounced effect on the activity of MSPC-5 and properties of PE;(3). New MgCl_2-Supported Single-Site Catalysts for Ethylene PolymerizationIn this work, a kind of new MgCl_2 support was obtained by anhydrous MgCl_2 co-milled with solid MAO, and it is a creative contribution. Then some single-site catalysts were supported on the new MgCl_2 support, and the resulted solid catalysts were tested in ethylene polymerization, the results indicated that:1.XRD and IR analyses indicate that MAO does be coordinated with MgCl_2, which is in good agreement with the results obtained by XPS;2.co-mlling time had no obvious effect on the texture of support after 12 hours;3.In this work, MgCl_2 was co-milled with solid MAO for different hours, and then complex 3 was supported on these co-milled supports. It was found that co-milling time markedly influences the activity of solid catalysts, but it had negligible effect on the kinetic profile and the properties of resultant PE.

XPS研究结果表明,MAO不仅仅只和乙醇作用,MAO还与MgCl_2本身有一定的作用,这是一个极为重要的发现;3、通过ICP和EDX表征,发现载体的脱醇温度直接影响着元素在固体催化剂中的含量及分布;4、脱醇温度极大地影响着负载苯氧基亚胺类催化剂的活性和聚合物的性能,特别是原始载体经160℃活化4小时制备得到的固体催化剂MSPC-5的活性明显高于其他脱醇温度条件下制得的固体催化,并且催化剂寿命长,表现出稳定的动力学行为,最终获得了高堆密度(大于0.35g/ml)的球形聚乙烯颗粒;5、本文选择MSPC-5为研究对象,考察了聚合反应参数对催化剂的活性及其聚合物的影响,研究发现:不同的烷基铝对催化剂具有非常重要的影响,特别足TIBA对MSPC-5的助催化活性最高,烷基铝的加入量有一个较佳值,聚合温度为80度时活性最高,H_2的加入使催化剂的活性明显降低且聚合物的分子量也减小;、新型氯化镁载体负载单活性中心催化剂催化乙烯聚合本文创造性采用固体MAO与无水氯化镁直接进行共研磨,制备出了一种的新型的氯化镁载体,并将该载体用于多种单活性中心催化剂的负载化研究,研究表明:1、通过BET、XRD的表征,再次证实了MAO与MgCl_2之间具有直接作用,与XPS的研究结果相一致;2、当研磨时间高于12小时时,延长研磨时间对载体的结构没有显著的影响;3、将配合物3负载于共研磨时间不同的一系列载体上,乙烯聚合结果表明,尽管共研磨时间对负载催化剂的活性具有明显的影响,但是它对聚合物的性能以及催化剂的影响不明显。

Dealcoholization temperature markedly influences the surface area and porosity of the resultant MAO-supports. When the support was pretreated at lower or higher temperature, the corresponding MAO-support shows very low surface area; 2.XRD and IR analyses indicate that MAO has reacted with the residual ethanol in the supports, which is an important manner to get MAO fixed on the carrier. Morever, XPS analyse indicates that MAO can also be coordinated with MgCl_2, which is another way to get MAO fixed on the support; 3.ICP and EDX analyses indicate that dealcoholization temperature not only determined the element content on the solid catalyst, but also influences the element distribution on the carrier; 4.The activities of the supported phenoxy-imine catalysts and the properties of resultant polymers are strongly dependent on the dealcoholization temperature. The support (MSP-5) obtained by treating MgCl_2·2.56C_2H_5OH at 160℃for 4 h, then modified by MAO is very effective for immobilizing complex 3, the resultant solid catalyst (MSPC-5) shows very high activity in ethylene polymerization, and its kinetics of polymerization is stable during the reaction process. Finally, PEs with spherical morphology and high bulk density (over 0.35g/ml) were obtained, without reactor fouling; 5.In this work, polymerization conditions such as alkylaluminums, Al/Zr ratio, temperature and H_2 had a pronounced effect on the activity of MSPC-5 and properties of PE;(3). New MgCl_2-Supported Single-Site Catalysts for Ethylene Polymerization In this work, a kind of new MgCl_2 support was obtained by anhydrous MgCl_2 co-milled with solid MAO, and it is a creative contribution. Then some single-site catalysts were supported on the new MgCl_2 support, and the resulted solid catalysts were tested in ethylene polymerization, the results indicated that: 1.XRD and IR analyses indicate that MAO does be coordinated with MgCl_2, which is in good agreement with the results obtained by XPS; 2.co-mlling time had no obvious effect on the texture of support after 12 hours; 3.In this work, MgCl_2 was co-milled with solid MAO for different hours, and then complex 3 was supported on these co-milled supports. It was found that co-milling time markedly influences the activity of solid catalysts, but it had negligible effect on the kinetic profile and the properties of resultant PE.

XPS研究结果表明,MAO不仅仅只和乙醇作用,MAO还与MgCl_2本身有一定的作用,这是一个极为重要的发现; 3、通过ICP和EDX表征,发现载体的脱醇温度直接影响着元素在固体催化剂中的含量及分布; 4、脱醇温度极大地影响着负载苯氧基亚胺类催化剂的活性和聚合物的性能,特别是原始载体经160℃活化4小时制备得到的固体催化剂MSPC-5的活性明显高于其他脱醇温度条件下制得的固体催化,并且催化剂寿命长,表现出稳定的动力学行为,最终获得了高堆密度(大于0.35g/ml)的球形聚乙烯颗粒; 5、本文选择MSPC-5为研究对象,考察了聚合反应参数对催化剂的活性及其聚合物的影响,研究发现:不同的烷基铝对催化剂具有非常重要的影响,特别足TIBA对MSPC-5的助催化活性最高,烷基铝的加入量有一个较佳值,聚合温度为80度时活性最高,H_2的加入使催化剂的活性明显降低且聚合物的分子量也减小;、新型氯化镁载体负载单活性中心催化剂催化乙烯聚合本文创造性采用固体MAO与无水氯化镁直接进行共研磨,制备出了一种的新型的氯化镁载体,并将该载体用于多种单活性中心催化剂的负载化研究,研究表明: 1、通过BET、XRD的表征,再次证实了MAO与MgCl_2之间具有直接作用,与XPS的研究结果相一致; 2、当研磨时间高于12小时时,延长研磨时间对载体的结构没有显著的影响; 3、将配合物3负载于共研磨时间不同的一系列载体上,乙烯聚合结果表明,尽管共研磨时间对负载催化剂的活性具有明显的影响,但是它对聚合物的性能以及催化剂的影响不明显。

Rheological behaviours have been investigated by means of Haake torque rheometer and AG-10TA universal testing machine. It has been showed that the melt viscosity of PVC/carboxylic ester rare earth salt compound is some greater than that of PVC/organotin mercaptide compound, which can not bring unfavourable consequences at the processing level.

用HAAKE转矩流变仪,AG-10TA万能材料试验机的流变装置对两种稳定剂与PVC的复合物的流变性能进行比较,发现羧酸酯稀土与PVC复合物的熔体粘度在相同实验条件下比有机硫醇锡与PVC复合物的熔体粘度略大,但不会带来加工上的困难。

In this paper analyzing stationary structures of NH~+_(4)H_(2O_(n=1~6) clusters,it is found that the first stationary structure is linear hydrogen bonding NH~+_(4) with H_(2)O in clusters,the second is bifurcated structure ,the third is trifurcated structure.

利用密度泛函理论中B3LYP方法,6-31G基组对NH4+(H2O)n(n=1~6)簇合物进行几何优化,得到了稳定结构。本论文分析了NH4+(H2O)n(n=1~6)簇合物的稳定结构,发现NH4+与H2O以线性氢键结合成的簇合物结构最稳定,其次是二叉结构,再次是三叉结构

The fluorescent emission mechanism, and the some factors that affect the energy and the intensities of the fluorescent peaks were studied. The strong powder second harmonic generation efficiencies for complexes (1),(2),(3) and (4) were found. The determination of variable-temperature magnetic susceptibility for complex (3) and complex (5) was performed. The magnetic data were analyzed with their structure properties, and the further information about the magnetic coupling capacity of Carbamyldicyanomethanide as bridging ligand was obtained.

测试了配合物(1),(2),(3),(4)的荧光光谱,从配体的结构特点等方面研究了该荧光光谱的产生机理,研究了影响荧光谱峰能量及强度的因素;发现了配合物(1),(2),(3),(4)显示有强的二阶非线性倍频效应;测试了配合物(3)和(5)的变温磁化率,对所得磁数据进行了结构性质分析,进一步获得了甲氨酰二氰基甲基阴离子作为桥联配体的磁耦合信息。

It was shown that the absorption peaks of amine and amide groups of gelatin were shifted in HDPE/PE-g-MAH/Gelatin blends because of the reaction of PE-g-MAH with gelatin. The addition of PE-g-MAH made the increase of HDPE glass transition temperature. The compatibilizing effect of PE-g-MAH was due to the crystal compatibility produced by forming the co-crystals of HDPE, PE-g-MAH and PE-g-MAH-g-gelatin. The blends of EAA and gelatin were prepared by melting process and the compatibility of the blends was also studied.

红外光谱分析结果表明:体系中明胶的氨基吸收峰、酰胺Ⅱ带吸收峰峰位发生了明显的变化;二甲苯和水抽提实验表明,在熔融共混过程中EAA与明胶发生了反应;DMA测试共混物的玻璃化转变温度发现:两组分的玻璃化转变温度差值减小;SEM的实验结果表明,共混物中明胶的表面有接枝物形成。

The interaction of two tetraaza nickel complexes in planar structures with DNA was investigated. It has been found that 〓 binds to DNA more strongly than 〓. The reason is that the open macrocycle of 〓 is more flexible to accommodate DNA with lesser obstacles.

对平面结构的镍配合物与DNA的作用机制进行了研究,发现开环结构的配合物〓比配合物〓容易使配体发生一定程度的扭曲,使之与DNA键合时所受到的空间阻力较小,因此与DNA的结合则较强。

The spectroscopic properties (λ〓〓,λ〓〓,φ,τ, k〓, k〓) of 〓 were also measured. It was found that the energies of absorption and emission maximum is red-shifted for both electron-withdrawing and electron-donating substituents compared to that of parent 〓 complex.

发现无论X是吸电子取代基还是给电子取代基,配合物的吸收峰和发射峰与母体化合物〓相比均向红移;常温下,具有吸电子基的配合物与具有给电子基的配合物相比,有较高的发光量子产率和长的激发态寿命。

Through XRD analysis, as the temperature of cosolvent and mass transport goes up, the wave peak intensify of tin dioxide becomes more obvious. By means of SEM, tin dioxide particulates are found evenly distributed on the matrix and the quantity of particulates become higher with the increasing cosolvent concentration. The size of particulates is about 30-50nm.

经XRD分析,复合材料中二氧化锡之波峰强度随潜溶剂浓度与质传温度之增加越趋明显;SEM观察则发现,二氧化锡颗粒析出物系均匀分布於基材内,且析出物的含量随潜溶剂浓度增加而增加,析出物的尺寸约30-50nm。

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Finally, according to market conditions and market products this article paper analyzes the trends in the development of camera technology, and designs a color night vision camera.

最后根据市场情况和市面上产品的情况分析了摄像机技术的发展趋势,并设计了一款彩色夜视摄像机。

Only person height weeds and the fierce looks stone idles were there.

只有半人深的荒草和龇牙咧嘴的神像。

This dramatic range, steeper than the Himalayas, is the upturned rim of the eastern edge of Tibet, a plateau that has risen to 5 km in response to the slow but un stoppable collision of India with Asia that began about 55 million years ago and which continues unabated today.

这一引人注目的地域范围,比喜马拉雅山更加陡峭,是处于西藏东部边缘的朝上翻的边框地带。响应启始于约5500万年前的、缓慢的但却不可阻挡的印度与亚洲地壳板块碰撞,高原已上升至五千米,这种碰撞持续至今,毫无衰退。