查询词典 molar quantities

Each tooth crown mesiodistal size between the first molar and the opposite molar of 240 dental casts was measured by electric calliper.

由作者用数字游标卡尺对240例模型上下颌第一恒磨牙到对侧第一恒磨牙共二十四颗牙每牙最大近远中径进行测量。

Where the absorbance A is proportional to the concentration (c, in mol/L) of the solute, the length of the path the light travels through the sample, and the constant of proportionality,ε, called molar absorptivity coefficient (L mol-1 cm-1) or molar extinction coefficient

那里的吸收度A正比于溶质的浓度，l是通过样品的光路的长度，而比例常数ε叫做莫耳吸收系数(L mol-1 cm-1)或者莫耳消光系数。

The gasification efficiency increased and the molar fraction of H2 decreased with an increase in the reaction temperature. The decomposition of PVA was more complete at higher temperatures. At 24 MPa, 500℃ and 120 s, the TOC remove rate, the carbon gasification rate and the hydrogen gasification rate were up to 71.46%, 67.97% and 157.24% respectively. A change in the residence time had no significant effect on the molar fraction of gas production but an increase in the residence time could enhance the gasification efficiency of PVA. It was found that the intermediates were mainly alkane, cycloparaffin, aromatic hydrocarbons, and low-molecular weight acids. It was supposed that PVA was degraded into small molecules through breaking of C-C bonds. Parts of the molecules were converted into H2, CO, CH4 and CO2 while some was converted into aromatic hydrocarbons.

过程探索发现：反应温度的升高能提高PVA气化效率，但气体产物中H2的含量随反应温度的升高有所下降；随着反应温度的升高，PVA分解趋于彻底，在压力24MPa、温度500℃、停留时间120s的条件下，TOC去除率、有机碳气化率和氢气化率分别达到71.46%，67.97%和157.24%；停留时间的变化对气体产物含量没有明显的影响，但延长停留时间能提高PVA的气化效率；PVA气化反应中间产物主要为链状烷烃、环烷烃、芳香烃及小分子酸，根据中间产物出现的顺序推测PVA的降解为由C-C键断裂形成小分子物质，这些小分子物质一部分转化为H2，CO，CH4和CO2，一部分形成难降解的芳香族化合物。

The study shows that: when the Cl-/SO42-molar rate is 1∶1, the Fe/Si molar rate is 2∶1, the flocculence has the best effect on paper-making waste water treatment.

本研究以废弃物为原料，合成新型絮凝剂，来处理造纸废水，旨在倡导循环经济。

The polysilicic acid is compounded with polyferric chloride sulphate under certain conditions, then the polysilicic acid-polyferric chloride sulphate flocculence is prepared. The study shows that: when the Cl-/SO42-molar rate is 1:1, the Fe/Si molar rate is 2:1, the flocculence has the best effect on paper-making waste water treatment.

将聚硅酸与聚合硫酸氯化铁在一定条件下复合，制备聚硅酸聚合硫酸氯化铁复合型絮凝剂，研究表明：在氯根与硫酸根物质的量比为1：1，且铁与硅物质的量比为2：1时，制得的复合型絮凝剂对造纸废水具有最佳处理效果。

The protrutive relation was set to reestablished the articulation. The geometry model constructed in CAD software was put into MSC.PATRAN to set the concrete Three-dimensional Finite Element Model. Result revealed (1) Tensile stress distributed in the posterior-upper area; molar area.(2) Compressive stress distributed in the opsile molar area and gonion area .

本研究通过模拟下颌前伸时，对下颌骨骨组织应力变化进行三维有限元分析[3 ，8] ，了解下颌骨骨组织应力分布特点，为临床矫形治疗提供理论依据。1 材料与方法1.1 建立几何模型1.1.1 病例选择选择一名年龄 12岁的男孩，X线手腕骨片显示处于生长发育高峰前期，全身发育正常。

The main content of this paper as follows: The acidic strength, reaction temperature, reaction time of Chlorine-aluminate Ionic Liquids with different structure of cation on the activity of transalkylation of MN with TeMB and the selectivity of 2,6-DMN were studied. The optimum reaction condition was obtained: the molar fraction of AlCl_3 is 0.71, molar ratio of 2-MN and TeMB is 1, the amount of ionic liquid is 32wt%, reaction temperature is 20℃and reaction time is 8h using X-xAlCl_3 and X-xAlCl_3 as catalysts; the optimum reaction time is shortened 6h using Et_3NHCl-xAlCl_3 as catalyst.

本文主要研究了以下内容：分别考察了不同阳离子结构的氯铝酸盐类离子液体的酸强度、反应温度、反应时间等因素对MN和TeMB转移烷基化的催化反应活性和2，6-DMN选择性的影响，优化得到适宜的反应条件为：以X-xAlCl_3和X-xAlCl_3为催化剂时，AlCl_3的摩尔分数x=0.71，2-MN和TeMB摩尔比为1∶1，离子液体用量为32wt％，反应温度为20℃，反应时间为8h；以Et_3NHCl-xAlCl_3为催化剂时，反应时间缩短到6h。

Results show that 4-oxo-β-ionone is the major product with yield of 53.5% under the conditions as follows: reaction temperature 45℃, reaction time 24 h, the molar ratio of n: n(NaClO3): n 20: 100: 3, and pH value of solution in 1-3; on the other hand, 5,6-epoxy-β-ionone is major product with yield of 25.4% when reaction temperature is 40℃, reaction time is 24 h, the molar ratio of n: n(NaClO3): n is 20: 120: 5, and pH values of solution is 3. The excessive β-ionone can be recovered by vacuum distillation for reusing again. 4-oxo-β-ionone and 5,6-epoxy-3-ionone were purified by recrystallization and silica gel column chromatograph respectively with the purity over 98%.

研究结果表明：氯酸钠氧化β-紫罗兰酮的反应主要生成4-氧代－β-紫罗兰酮和5，6-环氧－β-紫罗兰酮，经重结晶和硅胶柱层析分离，纯度高于98%；4-氧代－β-紫罗兰酮的有利合成条件是反应温度为45℃，反应时间为24h，溶液的pH值为1~3，反应物配比n：n(NaClO3)：n为20：100：3，最佳收率为53.5%；5，6-环氧－β-紫罗兰酮有利的合成条件是反应温度为40℃，反应时间为24h，溶液的pH值为3，反应物配比n：n(NaClO3)：n为20：120：5，其收率为25.4%；未反应的β-紫罗兰酮经减压蒸馏回收后可重复使用。

Based on the method of BCA, we menstruate the molar extinction coefficient of R-PE. The molar extinction coefficient in the wavelength of 565nm and 280nm is 4.75X K^mor'cm"1 and 4.07 X104morIcm"1 respectively.

在BCA法进行蛋白质定量的基础上，测定了R-PE的565nm和280nm的摩尔消光系数，它们分别为4.75×10~5mol~(-1)cm~(-1)和4.07×10~4mol~(-1)cm~(-1)。

The better technology has been obtained: taking water-EG as solvent 2-imidazolidinone was prepared. The molar ratio of the methanal (36%) to the formic acid (85%) is 1:2.8, reaction temperature is 95~100℃, reaction time is 16 h, taking cuprous chloride and triethylamine as catalyst, the molar ratio of the cuprous chloride and triethylamin to 2-imidazolidinone is 1.0% while 1,3-DMI was prepared.

较佳工艺条件为：制备2-咪唑啉酮时，以水－乙二醇混合作溶剂；制备1，3-DMI时，甲醛(36%)：甲酸(85%)摩尔比为1：2.8，反应温度95~100℃，反应时间16 h，氯化亚铜和三乙胺作催化剂，用量分别是2-咪唑啉酮摩尔数的1.0%。

Aquatic or marsh-growing fern allies; known to have existed since the Cenozoic; sometimes included in Lycopodiales.

生活于水中或湿地的蕨类；从新生代生存至今；有时归于石松目之中。

The engine was uprated from a 90hp Franklin to a 125hp Lycoming.

改良过的引擎是从90hp到125hp莱康明富兰克林。