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methanol相关的网络例句

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与 methanol 相关的网络例句 [注:此内容来源于网络,仅供参考]

The experimental results indicate that methanol synthesis gas can be produced by steam gasification of lauan sawdust at 680℃ without catalyst addition. However, in the presence of steam reforming catalyst (RKNR+RKS-1), weight ratio of catalyst to dry wood sawdust =1, methanol synthesis gas can be produced at 580℃.

实验结果显示:未加触媒时,本屑在680℃气化所产生的气体可用於甲醇的合成;而使用蒸气重组触媒(RKNR+RKS-1),在580℃、触媒与全乾木屑的重量比为1时,所产生的气体即可用於甲醇的合成。

Space time yield of methanol and concentration of methanol in the liquid product increased with increasing pressure.

随压力升高,甲醇产率及液相产物中的浓度逐渐升高。

The temperature of the zeolite structure damage is at 1169℃.According to the sorption isotherms, hexane and methanol are adsorbed in the ten-membered ring channel. Methanol molecules can enter the small cage through the eight- membered ring window at high partial pressure. The adsorption of water correlates to Si-OH defect and concentration of cations in the zeolites.

吸附现象表明,正己烷和甲醇都被吸附于FER沸石的十元环主孔道中,分压较高时,甲醇可通过八元环进入小笼,而水的吸附性质则主要与各样品的Si-OH缺陷及骨架中的阳离子含量有关。

The optimum reaction conditions were found finally. The results showed that the suitable conditions are under methanol solvent reaction temperature 40℃,the concentration of catalyzer TS-1 0.6%.,reaction time 60 minutes,propylene pressure 0.4Mpa under methanol solvent.Under Supercritical fluid system,the reaction temperature was 33.7℃(supercritical and near critical temperature),the reaction pressure was 7.58Mpa(near critical pressure and critical pressure range. propylene ), propylene pressure 0.65Mpa, reaction time 45min, cosolvent molality 4%.

而超临界体系下反(来源:4e56ABC论文网www.abclunwen.com)应温度适宜在近超临界和临界温度(33.7℃)以上,反应压力也是接近临界压力或者处于临界压力范围(7.58Mpa),丙烯压力是0.65Mpa,反应时间45min,共溶剂甲醇摩尔浓度4%,在此反应条件下,反应的转化率98%,选择性96%,收率94%,与传统条件相比较,收率提高了20%左右。

The optimum conditions for extraction was proved practicable by condition filtration and orthogonal design with supersonic wave method .The results showed that the optimum conditions for extraction to ultrasonic method is : methanol (φ=40,20ml),and 15℃ for 30 min ,this paper has determined nicotine contents that is 23.50mg/g at absorption peak (λ=262nm) by HPLC with an eluent consisting of methanol –potass Phosphate alleciate (pH=3) with the recovery and coefficient of variation are 101.52% and 0.91%.

通过超声波提取方法进行条件筛选和正交化实验,确定了烟草中尼古丁的最佳提取条件,结果表明,超声波最佳条件是:甲醇浓度40%,固液比1:20,提取时间30 分钟,超声温度15℃,用高效液相色谱方法在波长262nm 处测定尼古丁的含量,流动相组成为甲醇:磷酸二氢钾缓冲溶液=10:90,测得烟草中尼古丁的含量为23.50 mg/g,平均回收率为101.52%,相对偏差为0.91%。

In the case of racemate 2, better resolution was obtained when using 2-propanol as modifier in the place of methanol and ethanol, while for racemate 1, methanol provided the best performance. Both retention and resolution decreased with increase in pressure.

结果表明对映体的保留因子均随着改性剂含量的增加而显著下降,当改性剂含量大于10%时,保留因子的下降趋势变缓;分离帕罗酮酯时,异丙醇作改性剂的分离度和分离因子均最大,分离帕罗醇对映体时,甲醇是最佳的改性剂。

When the laser ablated Ni plasma acts on the head and tail of the beam, the metal methanol complex clusters Ni+(CH3OH)nand the oxidation clusters NiO+(CH3OH)n (n=1~15) together with protonated methanol clusters H+(CH3OH)n are domain.

发现NiO+(CH3OH)n是由Ni+(CH3OH)n团簇内的脱甲烷反应生成的,而H+(CH3OH)n、 H3O+(CH3OH)n主要是激光等离子体中的电子与甲醇团簇碰撞电离产生的。

Production United States AA level and GB338-92 high purity fine methanol, methanol middle Tank to Tank Farm.

生产出美国AA级和GB338-92高纯度的精甲醇,经中间罐区送到甲醇罐区。

The whole analysis was completed on a C〓 column in 18min at a flow rate of 0.5 ml/min, with the mobile phase of methanol-water (93: 7, v: v) containing 75 mmol/L TEOLA and 200 mmol/L HAc, or with the mobile phase of ethanol-water (90: 10, v: v) containing 25 mmol/L TEOLA and 200mmol/L HAc pumped at 0.25ml/min. Compared with the methanol system, the ethanol system was a better candidate for the separation of thulium porphyrin complexes in view of selectivity.

在C〓分析柱(5μm,2.5×150mm)上,流动相为:甲醇:水=93:7(v/v内含75mmol/L三乙醇胺和200mmol/LHAc),流速为0.5ml/min和流动相为:乙醇:水=90:10(v/v,内含25mmol/L三乙醇胺和200mmol/L HAc),流速为0.25ml/min,均能使六个铥卟啉配合物在18min内得到有效的分离,相比之下,乙醇体系对铥卟啉配合物更具有分离选择性。

The quantitation was monitored with an Inertsil ODS-3V column using a mobile phase of methanol- 0.3%acetic acid = 64:36 for TLM and acetonitrile- methanol - 0.3%acetic = 2:64:34 for Z detector set at 254nm.

对托美丁的分析方法是用Inertsil ODS-3V管柱,移动相则采甲醇: 0.3%醋酸为64: 36 ;而对佐美酸的定量亦用相同管柱,移动相为乙晴:甲醇: 0.3%醋酸为2: 64: 34,UV侦测器则同样设定为254 nm。

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