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溶解

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溶解牙石疗法:通过口含天然植物提练的牙齿黄金生物科技产品,无任何化学添加剂,无异味,无需进入肠胃吸收,只需要通过口含后刷牙漱口就可以看到明显效果,使用简单,安全性高,属于无痛去石,原理就是通过从植物中提炼而出的精华成份,跟牙石这种化学衍生物发生反应,从而达到深入牙龈溶解牙石的功效,牙结石脱落恢复牙齿表面原有的光泽,通过刷牙可将已溶解的龈下牙石清理出来,之后还能在牙齿表面加上一层保护膜,让牙石不再容易重新附着。

Based on the experimental results reported in literature, the dissolution and separation performance of ionic liquids for lignin, cellulose and hemicellulose are summarized. The relationship between structure of ionic liquids and their dissolution performance is analyzed, and the possible dissolution mechanism is discussed.

根据目前所报道的研究结果,总结了不同离子液体对木质素、纤维素、半纤维素的溶解作用以及对木质纤维素的分离性能,分析了离子液体的结构与其溶解性能的关系,讨论了可能的溶解机理。

Through the experiments on hydration of AH in the following sulphate(Li_2SO_4、MgSO_4 、 Al_2(SO_4)_3 、MnSO_4 、CuSO_4 、CoSO4 、CdSO_4 、ZnSO_4 、NiSO_4 、FeSO_4), dissoluble sulfate hydrate origining from hydration process of AH affects it's hydrous rate, hydrous rate of AH does not connect with Z/R of cation in stimulation, theory that Z/R affect hydrous rate of AH does not exist. Third, hydration of AH in dissoluble sulfate complies with dissolve-nucleate -grow theory, concentration of Ca~2+ from dissolving of CaSO_4 is higher than one of CaSO_4·2H_2O, calcium sulphate dihydrite gets a motivity of crystallization. dissoluble sulfate takes the following function: double-salt or dissoluble sulfate hydrate from hydration of AH in it becomes heterogeneous particle and a kind of nucleation catalyzer, and reduces surface barrier when DH becomes crystal because the crystal of DH precedently appears in uneven place. Results indicate hydration of AH does not conform with double-salt theory, but it conform with this mechanism: dissolve-nucleate-grow, formation of DH is an uneven nucleation and crystalizaion process.

通过对CaSO_4在Na_2SO_4 、K_2SO_4 、Rb_2SO_4 、Cs_2SO_4 、(NH_4)_2SO_4溶液中水化过程,以及CaSO_4·2H_2O、CaSO_4与以上硫酸盐反应速度、产物的研究,说明复盐理论不正确;CaSO_4在(Li_2SO_4、MgSO_4 、 Al_2(SO_4)_3 、MnSO_4 、CuSO_4 、CoSO_4 、CdSO_4 、ZnSO_4 、NiSO_4 、FeSO_4)溶液中水化,水化过程中硫酸盐水合物的析晶影响着无水硫酸钙水化,与激发剂阳离子Z/R值大小无关,阳离子的Z/R参数影响水化率的规律并不存在; 3、无水硫酸钙在可溶性硫酸盐中的水化按照溶解-成核-生长理论进行,CaSO_4达到溶解平衡时Ca~2+的浓度大于CaSO_4·2H_2O溶解平衡的Ca~2+的浓度,CaSO_4·2H_2O获得结晶的驱动力,可溶性硫酸盐起到形成晶核的作用:水化过程与CaSO_4生成复盐或析出水合物所形成的细小物相,作为异质微粒使母相中存在不均匀性,这些不均匀性有效地降低成核时的表面能位垒,使CaSO_4·2H_2O晶核优先地在这些具不均匀性的地方形成,因此这些物质起成核催化剂作用。

Iron oxides would continue to be formed or at least not to be dissolved under oxic conditions, and the sediments in brown to red color will then be dominant. While in a reducing environment, iron oxides will be dissolved, with the possible migration of iron ion in the ocean, and then buried as siderite, pyrite, or other ironbearing minerals.

氧化强氧化条件利于沉积物中氧化铁的持续产生或者至少保持不被溶解的状态,从而形成棕色-红色沉积物;还原条件利于沉积物中铁氧化物的溶解,形成菱铁矿、黄铁矿等形式的埋藏,并可能造成溶解铁在海洋内的迁移。

Bacterially triggered CDDS 细菌触发型细菌触发型 CDDS The presence of azo reductase enzymes play pivotal role in the release of drug from azo bond prodrugs while glycosidase activity of the colonic microflora is responsible for liberation of drugs from glycosidic prodrugs.

偶氮还原酶溶解酶的存在在偶氮键药释放过程中发挥关键作用,结肠菌群的糖苷酶活性负偶氮还原酶溶解酶的存在在偶氮键药释放过程中发挥关键作用,结肠菌群的糖苷酶活性负溶解释放过程中发挥关键作用的糖苷酶活性糖苷药物的解放。

It shows that gypsum is stable at the pressure less than 407 MPa; and then gypsum begins to dissolve with the increasing pressure. Gypsum stops dissolving and phase transition happens (gypsum-bassanite) to some degree. After phase transition, bassanite disappears with the rising pressure.

结果表明:压力小于407 MPa时,石膏的形态无明显变化;随着压力的升高,石膏开始溶解溶解至一定程度,石膏发生了向半水石膏转化的相变;相变完成后,半水石膏继续溶解至消失。

The results indicated that the erythropoietic/granulopoietic ratio was markedly increased with megaloblastic morphology in all stage of erythrocyte.

结果表明:2例CDAⅠ型患者骨髓幼红细胞比例增加,各阶段细胞存在不同程度巨幼样变;原红细胞核不规则,早幼或中幼红细胞可见奶酪核,约半数晚幼红细胞有核溶解和破碎现象,晚幼红细胞核损伤有时伴胞质溶解,细胞间染色质桥少见;各阶段红细胞核膜和内质网同时出现不同程度溶解

The study on dissolution rate and porosity of complete dissolution is important to investigae the solution mining mechanism of the difficult soluble glauberite.

溶解速率、溶解速度及溶解后孔隙率的研究对充分认识难溶性钙芒硝盐岩水溶开采机理有指导意义。

Solubility and stability of calcium arsenates under different CO2 pressures are studied based on the data of precipitation and solution experiments simulated by PHREEQC program. The result shows that calcium arsenates can dissolve incongruently by the effect of CO2 in high pH(pH〉8. 3)and make their solubility higher. The higher the CO2 pressure is, the lower the acidity of the incongruent dissolution is.

文章摘要:通过沉淀和溶解两方面的实验数据,应用PHREEQC程序模拟了砷酸钙在不同CO2分压条件下溶解度的变化情况,发现环境中的CO2可使砷酸钙盐在酸度较高(pH大于8.3)的条件下发生不一致溶解,使其溶解度升高;CO2分压越大,砷酸钙盐发生不一致溶解的酸度越低;CO2主要影响3:2和5:3的砷酸钙盐,而对4:2砷酸钙盐的影响较小。

By dehydrochlorination reaction the poly[(2-methoxyl-5-octyloxy)phenylene vinylene] is synthesized and the material"s structure is characterized by nuclear magnetic resonance spectroscopy, infrared absorption spectrum, ultraviolet and visible spectrophotometry. At the meantime, the fluorescence spectrum is measured and the mechanism of fluorescence occurring is analyzed. Thermal Gravimetric Analyzer"s results show that the MO-PPV"s thermal stability is fine. Also the experiment of resolvable property indicates that the MO-PPV can well dissolve in chloroform. Through analyzing the film"s surface by Metaloscope and Atomic Force Microscope, the good filming is found.

通过脱氯缩合法合成了聚(2-甲氧基-5-辛氧基)对苯乙炔,并分别用核磁共振波谱法、红外吸收光谱法、紫外-可见分光光度法等对其进行了结构表征;测量了样品的荧光光谱,分析了荧光产生的机理;热失重仪分析了材料的热稳定性,研究表明MO-PPV材料具有良好的热稳定性;溶解性实验发现材料在氯仿中溶解性较好;金相显微镜和原子力显微镜研究了薄膜的表面形貌,发现该材料的成膜性良好;材料的导电性研究表明,固体材料在掺杂下才可以表现出导电特性,而配成溶液的材料导电性因溶剂的不同而不同,并随溶解时间的长短发生变化。

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