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molar相关的网络例句

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与 molar 相关的网络例句 [注:此内容来源于网络,仅供参考]

Cases that are level from first molar to first molar will still show a deep overbite.

案件的级别从第一磨牙先摩尔仍然显示出深覆。

The calculation method represented in this paper is very simple and convenient. By comparing the relative errors, the method is better than other methods. Moreover, it can be used to calculate molar Gibbs free energy and molar enthalpy of formation of all complex oxysalt minerals including a series of titanate whiskers that author's group has studied for many years. The thermodynamic data for the series of titanate whiskers provide necessary fundamentals to their preparation.

本文提出的方法计算步骤十分简单,从相对误差来看,本方法和其他方法相比精度较好,可以计算包含本课题组长期研究的钛酸盐系列晶须的所有复杂含氧盐矿物的摩尔生成Gibbs自由能和摩尔生成焓,为热力学在钛酸盐系列晶须制备中的应用提供理论支持。

Hainan Industrial Co., Ltd., general manager of the first molar崔阳assistant told reporters that the first molar Hainan Department Store main shop "Causeway" will be opened December 25 this year, the news industry brought to Hainan's another strong shock .

海南实业有限公司总经理助理第一磨牙崔阳告诉记者,海南第一摩尔百货主店"铜锣湾"将于12月25日开幕,今年的新闻行业带到海南的另一个强有力的冲击。

Objective: To observe if there is the existence of a third root canal in the distal root of the mandibular first molar so as to avoid the clinical treatment of mandibular first molar root canal in the distal root left to provide guidance.

目的:观察下颌第一磨牙远中是否存在第三根管,以期为临床治疗中避免下颌第一磨牙远中根管的遗漏提供指导。

The invention relates to a process for producing polyethylene terephthalate 1, 3-propanediol, which comprises the following steps: using titanic acid ester as major catalyst, using germanium compounds and cobalt compounds as synergic catalyst, conducting esterification reaction for poly terephthalic acid and 1, 3-propanediol according to the molar 1:1.05-2.2 under the nitrogen pressure of 0.1-0.4MPa and 230-265 DEG C, or conducting ester exchanging reaction for poly terephthalic acid and 1, 3-propanediol according to the molar ratio 1:1.8-2.2 in 160-220 DEG C, decompressing reaction to high vacuum 10-150Pa, wherein the final temperature of reaction is 265-275 DEG C, recovering to normal pressure with nitrogen to obtain the PTT product.

本发明涉及一种生产聚对苯二甲酸1,3-丙二醇酯的方法,采用以钛酸酯为主催化剂,锗化合物和钴化合物为协同催化剂,对苯二甲酸二甲酯和1,3-丙二醇按摩尔1∶1.05-2.2,在0.1-0.4MPa氮气压力和230-265℃下进行酯化反应,或对苯二甲酸二甲酯和1,3-丙二醇按摩尔比1∶1.8-2.2,在160-220℃进行酯交换反应,将反应减压至高真空10-150Pa,反应终温在265-275℃,用氮气恢复到常压,得到本PTT产品;大大缩短了反应时间,直接聚合制备特性粘度在0.7-1.05dL/g的PTT切片,使反应产物色相良好,PTT产品可用于纤维加工及工程塑料领域。

Phenyl or m -tolyl selenoamides reacted with functionalized α-haloacetic acid in 1∶1 or 1∶2 molar ratio with no catalyst in various alcohols to undergo a selenium transfer reaction. This reaction in dif-ferent molar ratios furnished the same C—Se—Se—C coupling products with a special structure bis diselenide. A new and facile method for synthesis of such bis(alkoxycarbonyl-methyl) diselenides with the advantages of mild reaction conditions, high yields, easy availability of starting materials and good chemical selectivity was provided.

芳基硒代酰胺与氯乙酸在各种醇中无催化剂下以1∶1和1∶2的比例投入,发生硒转移反应,不同原料投入比下的反应生成了同一种C—Se—Se—C偶联产物——具有多功能团的二烷氧羰基甲基二硒醚,提供了一种新的合成二烷氧羰基甲基二硒醚的简便方法,且反应具有条件温和、产率高、原料易得和选择性好等优点。

Methods: The three-dimensional finite element models of mandible molar and attrited molar were developedwith computer technique.

以电子计算机技术建立下颌磨牙及磨耗磨牙三维有限元模型。

This in vivo study was to examine the historical changes of implanted novel chitosan/collagen composite barrier for confirming the clinical feasibility. Four other commercial GTR membranes were chosen for comparison. Among the resorbable GTR membranes, BioMend Extend and Peri-Aid are collagen base, and GORE-TEX OSSEOQUEST is synthesized membrane, while GORE-TEX e-PTFE (Expanded polytetrafluoroethylene) is synthesized but non-resorbable. Beagle dogs were used as animal model. Buccal mucoperiosteal flaps were reflected in the bilateral mandibular premolar and molar areas. Buccal alveolar bone was reduced on 1st、2nd premolar and molar to a level 5 mm apical to the cemento-enemel junction. Root surface was denuded of periodontal ligament and cementum, and notches were placed at the bone level of each root. The tested GTR barriers were implanted in critical bone defect areas. Flaps were coronally positioned and sutured. Two beagle dogs were sacrificed each time as the designed time period after surgery. Histological and histometirc evaluation at 7 days、14 days、28 days、3 months were performed post-operatively to determine the healing response of each treatment modality.

本研究之目的在评估与工研院生医中心合作发展出可吸收性去乙醯几丁聚醣/胶原蛋白复合之组织导引再生膜片,并选择与可吸收性之BioMend Extend 及Peri-Aid 胶原蛋白膜片,和GORE-TEX OSSEOQUEST 合成高分子膜片,及不可吸收之GORE-TEX e-PTFE合成高分子膜片,等其他四种市售商品材料共同对照评估,应用8只年龄为12个月的雄性小猎犬,均分4组(分别为7天、14天、28天、3个月),为动物活体评估模式,在实验犬之左、右下颚第一、二小臼齿及大臼齿的颊侧区制造骨缺损后,分别植入组织导引再生膜片,依实验设定时间将小猎犬牺牲,取下缺损区骨头,以光学显微镜观察量测其牙垩质再生高度与齿槽骨再生高度之变化,以探讨其组织再生模式及评估新膜片在临床应用之适用性。

The different molar ratio of hexane diacid to terephthalic acid with the same molar diamine is designed to give the composites with different viscosity, thermal performance and the barrier properties. The 3-10 times of enhanced barrier properties of these polyerster based nanocomposites with this above MXD6T to pure polyester resins are first reported.

在相同摩尔二胺的情况下,不同摩尔比例的己二酸和对苯二甲酸使复合材料具有不同的粘度、热性能和阻隔性能,含有NMXD6T改性剂的聚酯其阻隔性能相对于纯聚酯提高了3-10倍。

After the oxidative polymerization of DMP,styrene was in-situ polymerized under the initiation of dibenzoyl peroxide and dicumyl peroxide,finally thermodynamically compatible PPO/PS alloy was prepared.When styrene content was 50 wt%,for the synthesized PPO/PS alloy the yield and the weight-average molecular weight were determined to be 95%and 1.7×10~5 for PPO,93%and 2.0×10~5 for PS,respectively.The influence of the concentration of DMP and catalyst,molar ratio of N/Cu, oxygen partial pressure,NaOH concentration and temperature on the initial polymerization rate(R_0) of DMP was studied.It was found that the initial polymerization rate of DMP increased with the concentration of DMP and catalyst. The initial polymerization rate increased with the molar ratio of N/Cu at first and then decreased.

通过测定DMP氧化聚合过程中氧气吸收量随时间的变化,研究了DMP和催化剂浓度、N/Cu摩尔比、氧气分压、氢氧化钠浓度及温度对水介质中DMP氧化聚合初始速率的影响,发现DMP氧化聚合初始速率与氧气分压的0.1次方成正比;DMP氧化聚合初始速率随DMP和催化剂浓度及温度的增加而增加;随氢氧化钠浓度和N/Cu摩尔比的增加DMP氧化聚合初始速率先增加后降低。

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