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1.The binary and ternary stability constants of DL-α-Alaninc with Cu(Ⅱ),Zn(Ⅱ),Ni(Ⅱ) and Cd(Ⅱ) were determined by pH polcntiometric titration at 37±0.1℃ and ionic strength 150mM/dm3.Potentiomeinc data were treated with ZPLOT,MAGEC,MINIQUAD and ESTA programs. The compositions of complex species were ascertained in the complex equilibriums by selection of different chemical models.
本文报导了用pH电位法在温度为37±0.1℃和离子强度为150mM/dm~3下研究了丙氨酸与铜、锌、镍、镉的二元和三元配合稳定常数,并确定了各体系中配合粒子的正确组成.收藏指正
2.Applying the computer program MINIQUAT and ESTA to the titration data the best chemical species models have been chosen in each systems and stability constants at physiological conditions (37±1°C and ionic strength I=150mmol·dm~(-3)NaCl) have also been determined.
电位滴定数据是使用MINIQUAD和ESTA计算机程序处理的. 在每个体系中确定了最佳配合粒子模型,并测定了在生理条件下(温度为37±0.1,℃离子强度为150mmol·dm~(-3)NaCl)的稳定常数.收藏指正
3.AgI nano-particles prepared by the complex
由配合制备AgI纳米粒子收藏指正
4.A very small object, creature, or particle.
微粒、微一个很小的体,动粒子收藏指正
5.Testing result showed that the coagulate particle content of PET with additive decreased markedly.
测试结果表明,引入添加后所得PET样品的凝聚粒子显著减少。收藏指正
6.muddiness created by stirring up sediment or having foreign particles suspended.
因沉淀被搅起来或有外部的粒子悬浮而造成的不透明的状态。收藏指正
7.T he hollow particles of Y(OH)CO 3 (see Fig.5)were prepared by the coordi-nation reaction which dissolved the pre-existing particles of AgI in Na 2 S 2 O 3 concentrated solutions.
并加入配合剂Na2S2O3,运用生成稳定配合的方法溶解内置核,最终得到Y(OH)CO3中空粒子.收藏指正
8.The laminations are usually bonded together by adhesives, but other forces could be used, such as those provided by welding.
纤维和粒子通过内聚力使其悬浮在基体中形成合成收藏指正
9.The morphology and phase of cadimum sulfide nano-particles are delected by SEM and X-ray diffraction. The results show that the CdS nano-particles are spherical and spinulous respectively. The spherical particles are poor crystalline with somewhal of oxidation, and the spinulous particles are wurtzite structure.
通过扫描电镜、X射线衍射分析了所得样品的形貌和相,结果表明所制备的硫化镉纳米粒子为球形和针状,其中,球形样品结晶程度低,部分样品被氧化,针状样品为纤锌矿型结构。收藏指正
10.Ultra fine ZnO particle film was prepared by the deposition method with DC gas discharge activating reaction, and their structure as well as particle size were analysed by XRD and SEM, the results showed that the sample is ZnO polycrystal, and the particle size is 88.5nm.
用直流气体放电活化反应沉积的方法,制备了氧化锌超微粒子薄膜,并经AES成分分析及XRD相结构鉴定,随制备条件不同,结构将明显改变。 扫描电子显微镜(SEM)分析结果表明,粒子的粒径为88.5nm。收藏指正
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