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mol.相关的网络例句
与 mol. 相关的网络例句 [注:此内容来源于网络,仅供参考]

In the sprayed concentration scope of 0~450μmol/L, the level of thesubstances rasied as the sprayed concentration rasied, but as the concentration increased to600μmol/L, the substance level are not raised obviously higher, and some of them get a little lower.

在0~450μmol/L的喷施浓度范围内,上述物质的含量随着MeJA浓度的增加而增加,600μmol/L的处理与450μmol/L的处理相比,没有明显的提高,且大多数表现出含量略微降低。

Self-assembly of PEO-b-PB (M〓of PEO=5100 g/mol and M〓 of PB=5100 g/mol) and poly (PAA, M〓=2000 g/mol) was obtained in THF/dodecane mixtures via PEO/PAA complex. The effect of ratio of PEO-b-PB: PAA was investigated.

通过PEO-b-PB(PEO和PB分子量均为5100g/mol)中PEO链段和聚丙烯酸(PAA,分子量为2000g/mol)的氢键相互作用,我们在THF/正十二烷混合溶剂中获得了PEO-b-PB/PAA的自组装体,并研究了PAA用量对自组装行为的影响。

Using the improved method, the standard molal enthalpies of solution =-29.18 kJ·mol���1 in pure water and =-25.79 kJ·mol���1 in aqueous sulfuric acid were obtained, respectively.

借助VOSO4水溶液的离子缔合平衡和硫酸的二级解离平衡,改进了Archer方法,并用这种改进的方法分别估算了VOSO4·2.76H2O在水中的标准摩尔溶解焓=-29.18 kJ·mol-1,以及在0.5 mol·kg-1硫酸水溶液中的标准摩尔溶解焓=-25.79 kJ·mol-1。

The supernatant was removed. The wells were divided into five groups with 12 wells in each group. The control group was added with 1 g/L dimethyl sulphoxide and 3.3 mmol/L or 16.7 mmol/L glucose, 1 mL per well. The four experimental groups were added with 1 mL 0.2 μmol/L, 1 μmol/L, 5 μmol/L, or 10 μmol/L clozapine apart from the above DMSO and glucose.

每12孔为一组,共5组:对照组的孵育液含1 g/L二甲基亚砜、3.3 mmol/L或16.7 mmol/L的葡萄糖液1 mL;4个不同浓度氯氮平组的孵育液除含有上述成分外,还分别含浓度为0.2,1.0,5.0或10.0μmoL/L氯氮平;各组有6孔继续孵育1 h,另外6孔继续孵育4 h;吸取上清液,保存于-20℃冰箱中待测。

Results Compared with solvent control,toxaphene increased significantly MN frequencies in Hep G2 cells at concentrations of 20,40?μmol/L respectively(P.01,P.01).No significant increase of MN frequencies were found in Hep G2 cells treated with Aroclor1254(23~184?μmol/L) and DDT17.8~60?

结果20,40μmol/L毒杀芬处理Hep G2细胞的微核率与溶剂对照相比显著增加(P.01,P.01);经Aroclor1254(23~184μmol/L)和滴滴涕(17.8~60μmol/L)处理的Hep G2细胞的微核率与溶剂对照相比,差异无统计学意义。

Results AE from CM had vasodilating effect on the contracti on of mesentery blood capillary in guinea pigs and the contraction of rat thoracic aortic ring induced by l0μmol/L phenylephrine, even under the condition of pre-treating with glibenclamide (1μmol/L) or propranolol (3μmol/L). When the endothelium of the rat thoracic aortic ring was removed, AE from CM had not vasodilating effect hut constrictive effect. AE from CM could also increase the contents of NO, NOS and cNOS in the aortic tissue and had no obvious effect on the NO content in plasma and iNOS in aortic tissue of rats.

结果 桑白皮丙酮提取物有抑制去甲肾上腺素收缩豚鼠肠系膜微血管的作用,抑制苯肾上腺素(10μmol/L)收缩离体大鼠胸主动脉环的作用,预加优降糖或普蔡洛尔(3μmol/L)后仍然有松弛作用;大鼠胸主动脉环去内皮后药物无松弛作用,反而起收缩作用;显著升高血管的NO和NOS、cNOS含量,对大鼠血浆的NO和血管iNOS的含量影响不大。

Based on the retention and Z (the number of solvent molecules involving in t he displacement from stationary-phase surface ), log I (a constant relating t o the affinity of 1 mol of solute to the bonded stationary phase ), and j (a const ant r elating to the affinity of 1 mol of solvent to the bonded stationary phase ), th e elution strength of acetic acid-water mobile phase was found to be stronger th a n that of methanol-water-TFA.

用参数Z (1 mol溶剂化溶质被溶剂化固定相吸附时从两者接触表面释放出置换剂的摩尔总数),log I (与1 mol溶质对固定相亲和势有关的常数)和j(与1 mol溶剂对固定相亲和势有关的常数)对9种蛋白质在此流动相体系中的保留进行了表征。

Mol��L -1 SA treatment significantly inhibited activities of IAA oxidaseand ascorbate oxidase, while 200 μmol��L -1 and 400 μmol��L -1 SA t...

SA 1 0 0 μmol·L-1 的处理显著抑制了IAA氧化酶和抗坏血酸氧化酶的活性,而SA 2 0 0和 4 0 0 μmol·L-1 的处理则有促进作用。

According to the experimental results the reaction mechanism of gasification is proposed: firstly, the catalyst releases an oxygen atom from its rich-oxygen site to combine with a carbon atom and create a CO, then the CO molecule desorbs from the catalyst surface; next, the catalyst absorbs a CO2 molecule; and finally on the catalyst surface another CO molecule is created and the original rich-oxygen site gets an oxygen atom. On the basis of gasification process the material balance equations were built, which were solved by using numerrical integral methods and the reaction rate constants for four steps were obtained: they are 0.0703mol��g-1·min-1·kPa-1, 0.0959mol��g-1·min-1·kPa-1, 0.00539 mol��g-1·min-1 and 0.0321 mol��g-1·min-1·kPa-1 respectively.

根据实验结果推导得出了该反应过程是催化剂表面富氧活性部位先与煤焦反应生成一个CO分子,然后此CO分子从催化剂表面脱附,接着催化剂吸附气态的CO2生成一个CO并且夺得一个氧原子实现自身还原的过程,在此基础上建立了煤的催化气化的物料平衡方程组,对各步骤的反应速率常数进行了求解,在本文采用的实验条件下,各反应步骤的反应速率常数分别为0.0703 mol·g-1·min-1·kPa-1;0.0959 mol·g-1·min-1·kPa-1;0.00539 mol·g-1·min-1·kPa-1; 0.0321mol·g-1·min-1·kPa-1。

The two competitive reactions both consist of two steps, two reactants firstly form a three-membered ring intermediate (INT1) and a twisted four-membered ring intermediate (INT2), respectively, both of which are barrier-free exothermic reactions of 41.5 kJ/mol and 72.3 kJ/mol; then INT1 isomerizes to a four-membered ring product (P1) via transition state (TS1), and INT2 results in the chlorine-transfer product (P2) via transition state (TS2), with the barriers of 2.9 kJ/mol and 0.3 kJ/mol, respectively.

INT1和INT2分别经过渡态TS1和TS2异构化为了四元环产物P1和生成了氯迁移产物P2,其势垒分别为2.9和0.3 kJ/mol。

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