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峰上升
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  “峰上升”译为未确定词的双语例句
     The α-peaks decline and the β-peak raises when the reaction is in process.
     随着反应进行,α峰下降而β峰上升
短句来源
     The results showed that in all cases left and right ventricular systolic function and both size of ventricle were normal while in 30 cases of hypertension I patient han easly peak velocity(E) was lower Atrial pear velocity(A) was higher, ratio of E/A was lower Rapid Filling Fraction (RFF) and 1/3 Filling Fraction (1/3 FF) were lower, Deceleration Time (DT) was prolonged.
     以统一标准严格测定,结果显示30例早期高血压病例代表左右心室舒张功能的指标均有不同程度改变,主要表现为E峰下降,A峰上升,E/A比值降低,RFF、PFR、1/3 FF减少和DT延长,与正常对照组比较统计学上有显著性差别(P<0.05)。
短句来源
     In XANES spectra of the samples calcined at 950 ℃, the shoulder peak (1s→4s) can be detected.
     950℃焙烧的样品 ,在主吸收峰上升过程中出现了肩峰 ( 1 s→ 4s) .
短句来源
     The result showed that there was an obvious inhibiting action to the ascending amplitude of FSH and LH in experimental group.
     结果:实验组FSH和LH峰上升的幅度有明显的抑制现象,2组峰上升速度的比较,经统计学处理,P<0.001;
短句来源
     Objectives To investigate the value of noninvasive assessment of left ventricular dias-tolic function in patients with hypertension heart disease by pulmonary venous flow (PVF).
     使用频谱多普勒记录肺静脉和二尖瓣口血流频谱及心功能的有关参数,观察各组病人肺静脉血流速度的变化和左室舒张功能的关系。 结果 高血压组PVF频谱参数较对照组有显著差异(P<0.05),表现为PVd峰下降,PVs峰上升,PVs/PVd>1,PVa峰升高。
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  相似匹配句对
     Moreover, the peaks current increased with the concentration of Cr(VI)-GSH complexes and incubation time.
     -GSH配合物浓度增加电流上升
短句来源
     In addition,there also exist C=C vibra tion peak as the result of the de-hydrogen chloride reaction.
     C振动
短句来源
     The α-peaks decline and the β-peak raises when the reaction is in process.
     随着反应进行,α下降而β上升
短句来源
     (3)It could be operated for peak power modulation and power factor correction.
     可调、调相;
短句来源
     s to2mPa. s.
     s上升到2mPa.
短句来源
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Under a certain experimental condition, a-type of heavier rare earths chelates of chlorophosphonazo (III) can be converted to β-type. In continuous scanning spectrogram, it is shown that α-type is formed instantaneously. The α-peaks decline and the β-peak raises when the reaction is in process. when Yb:R = l :1 and pH = 3.2, we had determinated at constant temperature that the order of reaction is equal to 2 and 1 for nonbuffer system and buffer system (NaAc-HCl) while apparent activation energy is equal to...

Under a certain experimental condition, a-type of heavier rare earths chelates of chlorophosphonazo (III) can be converted to β-type. In continuous scanning spectrogram, it is shown that α-type is formed instantaneously. The α-peaks decline and the β-peak raises when the reaction is in process. when Yb:R = l :1 and pH = 3.2, we had determinated at constant temperature that the order of reaction is equal to 2 and 1 for nonbuffer system and buffer system (NaAc-HCl) while apparent activation energy is equal to 71.7 KJ/mol and 49.8KJ/mol, respectively. For many buffer systems of interest, it is clear that buffer medium of having nucleophilic groups can accelerate the converted process. In these buffer systems the observed formation rate of β-type chelates decreases with increasing of hydrogen ion concentration and increases with the buffer medium concentration. The experimental result tells us that two a-type molecules combine into a β-type molecule and liberate a proton at the same time. With these information, therefore, we can suggest a reasonable mechanism for nonbuffer system-and the differential rate equation, obviously, is-For buffer system a reasonable mechanism will be. The differential rate equation becomesIn accord with these results, we can satisfactorily explain all experimental facts. At last, the geometrical configuration and the reaction mode are discussed in this paper.

一定条件下,偶氮氯膦Ⅲ的重稀土螯合物可由α型转化成β型。连续扫描的谱图表明:α型是瞬时形成的。随着反应进行,α峰下降而β峰上升。在恒溫、Yb:R=1:1和pH=3.2时,测得非缓冲体系和缓冲体系(NaAc—HCl)的反应级数分别为2和1,表观活化能分别为71.1KJ/mol和49.8KJ/mol。对于许多缓冲体系,具有亲核基团的缓冲介质能够加速此转化过程。在此缓冲体系中,β型螯合物的生成速率随氢离子浓度的增大而减小,随缓冲介质浓度增大而增大。实验还表明:两个α型分子形成一个β型分子并释放出一个质子。据此,对缓冲体系和非缓冲体系分别拟出了合理的机理,稳态处理后的动力学速率方程满意地解释了所有实验事实。最后讨论了反应机理的可能模式。

The properties of chlorophosphonazo-m-COCH_3(CPAmA)and the composition,absorption spectrum and overall stability constant of its α-type complex with praseodymium are studied with spectrophotometric method. The formation of α-type complex of Pr-CPAmA has a relatively wide metal/ reagent mole ratio and wide pH range.The complex takes place quickly and is also very stable.But,the β-type complex is formed from α-type complex at the mole ratio of Pr/CPAmA 1.0~2.5 and pH range 1.68~2.10.Kinetic studies indicate that...

The properties of chlorophosphonazo-m-COCH_3(CPAmA)and the composition,absorption spectrum and overall stability constant of its α-type complex with praseodymium are studied with spectrophotometric method. The formation of α-type complex of Pr-CPAmA has a relatively wide metal/ reagent mole ratio and wide pH range.The complex takes place quickly and is also very stable.But,the β-type complex is formed from α-type complex at the mole ratio of Pr/CPAmA 1.0~2.5 and pH range 1.68~2.10.Kinetic studies indicate that this is a first order reaction,its half time being 8.4 minutes and the apparent activation energy E_a= 29.98 kJ/mol.

文本报导用分光光度法研究间乙酰基偶氨氯膦的性质,及其与稀土元素镨的α型配合物的组成、吸收光谱、积累稳定常数(1gβ_3=49.59)。一定条件下镨的偶氮氯膦mA配合物可由α型转变为β型,α型是瞬时形成的,随着反应的进行α峰下降而β峰上升。在pH为2.02、Pr/CPAmA摩尔比为2∶1时,测得β型配合物形成反应的级数为一级,半衰期为8.4分,表观活化能为29.98kJ/mol。

The properties of chlorophosphonazo-m-COCH_3(CPAmA)and the composition, absorption spectrum and overall stability constant of its α-type complex with praseodymium are studied with spectrophotometric method. The formation of α-type complex of Pr-CPAmA has a relatively wide metal/ reagent mole ratio and wide pH range.The complex takes place quickly and is also very stable. But, the β-type complex is formed from α-type complex at the mole ratio of Pr/CPAmA 1.0~2.5 and pH range 1.68~2.10. Kinetic studies indicate...

The properties of chlorophosphonazo-m-COCH_3(CPAmA)and the composition, absorption spectrum and overall stability constant of its α-type complex with praseodymium are studied with spectrophotometric method. The formation of α-type complex of Pr-CPAmA has a relatively wide metal/ reagent mole ratio and wide pH range.The complex takes place quickly and is also very stable. But, the β-type complex is formed from α-type complex at the mole ratio of Pr/CPAmA 1.0~2.5 and pH range 1.68~2.10. Kinetic studies indicate that this is a first order reaction, its half time being 8.4 minutes and the apparent activation energy E_(α) = 29.98 kJ/mol.

文本报导用分光光度法研究间乙酰基偶氮氯膦的性质,及其与稀土元素镨的α型配合物的组成、吸收光谱、积累稳定常数(lgβ_s=49.59)。一定条件下镨的偶氮氯膦mA配合物可由α型转变为β型,α型是瞬时形成的,随着反应的进行α峰下降而β峰上升。在pH为2.02、Pr/CPAmA摩尔比为2:1时,测得β型配合物形成反应的级数为一级,半衰期为8.4分,表观活化能为29.98kJ/mol。

 
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