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One-axial loads as well as proportional and nonproportional multiaxial loads such as torsion and bending with and without phase shift (d= 0 deg and d=90 deg) were applied to the welded conxtruction samples.

一轴向负载,以及成比例和nonproportional multiaxial象扭并且有和没有相移(d = 0 度和d = 90 度)弯曲那样装被用于被焊接的conxtruction 样品。

A method is provided for manufacturing cleaner fuels, in which NPC, naturally existing in small quantities within various petrolic hydrocarbon fractions, are removed from the petrolic hydrocarbon fractions ranging, in boiling point, from 110 to 560 DEG C and preferably from 200 to 400 DEG C, in advance of catalytic hydroprocessing.

提供了一种生产清洁燃料的方法。该方法是在催化加氢处理之前,从沸点在110―560℃,较好在200―400℃范围的石油原料馏分中除去以少量存在的天然极性化合物。

The method adopts the following steps: after mixed, phosphorus source, silicon source, aluminum source, an organic template agent, water and a precursor of the SAPO molecular sieve are hydrothermally crystallized for at least 0.1 hour at the temperature ranging from 110 to 260 DEG C to obtain the SAPO molecular sieve; wherein, the preparation method for the precursor of the SAPO molecular sieve has the following steps:, the molar ratio is 0.03 to 0.6 R:(Si0.01 to 0.98: Al 0.01 to 0.6: P0.01 to 0.6): 2 to 500 H2O; wherein, R stands for mixture solution of raw materials which is blended by the phosphorus source, the silicon source, the aluminum source, the an organic template agent and water of the template agent;, the mixture solution of raw materials prepared in step reacts at the temperature which is at least 50 DEG C lower than the crystallization temperature for at least 0.1 hour.

本发明通过采用包括以下步骤:将磷源、硅源、铝源、有机模板剂、水和SAPO分子筛前驱体混合后在110~260℃的温度下水热晶化至少0.1小时获得SAPO分子筛;其中SAPO分子筛的前驱体的制备包括以下步骤:将摩尔配比为0.03~0.6R∶(Si0.01~0.98∶Al0.01~0.6∶P0.01~0.6)∶2~500H 2 O,式中R代表模板剂的磷源、硅源、铝源、有机模板剂和水混合成原料混合液;将步骤制备的原料混合液在低于晶化温度至少50℃的温度下反应至少0.1小时的技术方案较好地解决了该问题,可应用于含氧化合物制烯烃催化剂的制备过程。

The liquid crystal display has a chiral ferroelectric smectic liquid crystal between two transparent plates with electrodes for generating an electric field, and polarisers in front of and behind the liquid crystal, the ratio d/p of the thickness d of the liquid crystal layer to the pitch p of the helical twisting being larger than 5, the smectic tilt angle theta 0 being between 22.5 DEG and 50 DEG , and the product d.

一种液晶显示单元,它具有:一种在两块透明平板之间的手性铁电近晶液晶;用于产生电场的电极;在液晶前后各有一偏振片,液晶层的厚度d与螺距扭曲的螺距高度p的比值d/p大于5,近晶倾角θ 0 为22.5~50°,厚度d、倾角θ 0 的平方、双折射率△n和光波长λ倒数的乘积dθ 2 0 △n1/λ大于0.45μm。

The method is as follows: n-butyl titanate, absolute ethyl alcohol, surfactant and concentrated hydrochloric acid are fully mixed and stirred for 4 to 6 hours under room temperature to obtain precursor solution, then the precursor solution is spinningly coated on a clean conductive glass substrate of an indium oxide tin coating, and then the conductive glass spinningly coated with the precursor solution is preserved for 25 to 72 hours at the temperature of between 20 and 30 DEG C and the relative humidity of between 50 and 75 percent below, and finally undergoes a high-temperature calcination at the temperature of between 350 and 700 DEG C.

将钛酸正丁酯,无水乙醇,表面活性剂和浓盐酸充分混合,在室温下搅拌4小时-6小时得到前驱剂,然后将前驱剂旋涂在清洁的氧化铟锡镀层的导电玻璃基底上,接着在20℃-30℃,相对湿度在50%-75%下,将旋涂有前驱剂的导电玻璃保存24小时-72小时,最后经过350℃-700℃高温煅烧。

The invention discloses an electrochemical method for preparing a hydroxylapatite particle thin coating on the surface of a metal implant, which comprises the following steps: electrolyte is put into a container equipped with a constant temperature heating system and heated to be 30 DEG C to 95 DEG C, and then the temperature is kept; platinum is taken as the anode and evenly distributed around the container, and the metal implant is taken as the cathode, put in the middle of the container and totally soaked in the electrolyte; DC voltage of 2V to 4V is added between the anode and the cathode, the surface of the metal implant has cathode reduction reaction, the pH value is increased and the supersaturation degree of the hydroxylapatite is also increased, so as to crystalize on the surface of titanium; after 0.5h to 5h of deposition, a layer of hydroxylapatite particle thin coating which can be excellently adhered to the matrix metal is formed on the surface of the implant.

本发明公开了一种在金属植入体表面制备羟基磷灰石颗粒薄涂层的电化学方法,在装备了恒温加热系统的容器中装入电解液,并将电解液加热到30~95℃恒温;将铂作为阳极均匀分布在容器四周,金属植入体作为阴极置于容器中间,完全浸没在电解液中,两极之间加直流电压2~4V,金属植入体表面发生阴极还原反应,pH值升高,羟基磷灰石过饱和度增加,从而结晶在钛金属表面;经过0.5~5小时沉积后,在植入体表面即可形成一层与基体金属结合优良的、薄的羟基磷灰石颗粒薄涂层。

The invention comprises the following steps: one end of the optical fiber array is irradiated by an ultraviolet light for 5 seconds to 10 minutes and is put under 550 DEG C to 600 DEG C for 30 minutes to 5 hours; then is corraded by the acid.

本发明提供了一种生物芯片用光纤阵列的制备方法,包括以下步骤:将光纤阵列一端用紫外光照射5s~10min;然后在550℃~600℃下放置30min~5h;再用酸进行侵蚀。

A preparation method of the visible-light photocatalyst Bi2WO6 nano-powder is characterized by comprising the steps as follows:(1) the selection of raw materials;(2) bismuth nitrate Bi(NO33 question mark 5H2O is added into a citric acid solution to obtain the citric acid solution containing white sediment;(3) EDTA is added into ammonia water which is then added dropwise with the citric acid solution containing the Bi(NO3)3 question mark 5H2O so to obtain a solution of bismuth;(4) the solution of bismuth is added with (NH4)6W7O24 question mark 6H2O solution to form a precursor solution which is then stirred, dried, coked, cooled and ground to obtain decarburized powder;(5) the decarburized powder is roasted for 2h to 4h under 450 DEG C to 550 DEG C to obtain the visible-light photocatalyst Bi2WO6 nano-powder.

可见光催化剂Bi 2 WO 6 纳米粉体的制备方法,其特征在于它包括如下步骤:1原料的选取;2将Bi(NO 3 ) 3 5H 2 O加到柠檬酸溶液中,得到含有白色沉淀的柠檬酸溶液;3将乙二胺四乙酸加到氨水中,并缓慢滴加入含有Bi(NO 3 ) 3 5H 2 O的柠檬酸溶液中,得铋的溶液;4将(NH 4 ) 6 W 7 O 24 6H 2 O溶液加入上述铋的溶液中,组成前驱液;搅拌,干燥,焦化,冷却后,研磨,得去碳的粉体;5将去碳的粉体在450~550℃下焙烧2~4h后,得到可见光催化剂Bi 2 WO 6 纳米粉体。

The method comprises the procedures as follows:(1) the surface of a base plate is treated:(2) colloidal solution is prepared: and (3) the base plate is put into a vessel and the colloidal solution is added into the vessel; the colloidal solution volatilizes under the constant temperature of 20 DEG C to 70 DEG C; the photonic crystal is taken out until no substance volatilizes, and the photonic crystal is made.

本发明方法如下:一、基板的表面处理;二、胶体溶液的配置;三、将基板放入容器中,然后加入步骤二配置的胶体溶液,然后在温度为20℃-70℃的恒温条件下使胶体溶液挥发,待无物质挥发取出基板,即得到光子晶体。

Passive detection and precision guidance using long-wave IR beam with logical signal processing and automatic target tracking; simultaneous tracking of 20 targets with precision of 0.7 deg in elevation, 0.4 deg in azimuth, 50m in distance 春秋中文社区http://bbs.cqzg.cn

可利用長波長紅外線波束配合邏輯訊號處理與自動目標追蹤能力進行被動偵測與精確導引,可同時追蹤20個目標,精確度在50公尺以內垂直方向有0.7度,水平方位0.4度。

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