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By comparison among concentration of nitrogen compounds, relative contents of pryyolic N-H shielded carbazoles and parameters of C21-/C22+、Pr/nC17 , the results show that slight biodegradation has little effects on the relative contents and distribution of pyrrolic nitrogen compounds, but has certain effect on its concentration.

根据2类原油中含氮化合物浓度、屏蔽型含氮化合物的相对含量与反晕原油生物降解的地化参数C21-/C22+、Pr/nC17等指标的对比研究,发现生物降解作用对该区原油中含氮化合物的相对含量及其分布影响不显,运移作用仍然是造成含氮化合物分馏的主要因素。

The concentration of enantiomers was positively related to the maintenance dose of warfarin, but not to drug response. It is not applicable to adjustment of the dose by monitoring the concentration of racemic warfarin, or to its enantiomers.

异构物浓度与维持剂量间有显著的相关性存在,但与疗效间却没有直接的相关,故无法以监测浓度的方式来调整病患之剂量,仍需采用临床上使用的INR值来监测。

Regenerative process was determined by comparing the concentration difference of Na+ in used and unused regenerant, as well as the concentration of Na+ in hydrogen peroxide out of resin columns.

比较浸泡失效树脂前后再生剂中Na+浓度变化和工业级H2O2流经交换柱后Na+浓度,确定适宜的再生方法。

Using New Zealand rabbit ears cartilage makes chondrocyte suspension, Fibrinogen was mixed with D-hank's makes a final fibrinogen concentration of 50mg/ml mixture solution, then chondrocytes resuspend with fibrinogen solution, chondrocytes-seeded fibrinogen was mixed with thrombin (25U/ml in 40mM calcium choride) to make chondrocytes/fibrin glue polymer. Pluronic F-127 was mixed with D-hank's makes a final Pluronic F-127 concentration of 400mg/ml mixture solution, then chondrocytes resuspend with Pluronic F-127 solution to make chondrocytes/Pluronic F-127 polymer. The chondrocyte concentrations was 10 million chondrocyte/ml of polymer.

为确定纤维蛋白凝胶与Pluronic F-127在注射方式形成组织工程化软骨过程中的优劣,我们进行了如下实验:应用新西兰大白兔耳软骨获取软骨细胞并体外培养,纤维蛋白原应用D-hank's液配制为50mg/ml,然后以纤维蛋白原溶液重悬软骨细胞,再与40mM的氯化钙配制的25U/ml凝血酶混合形成软骨细胞—纤维蛋白凝胶复合物;Pluronic F-127应用D-hank's液配制为400mg/ml,同样用PluronicF-127溶液重悬软骨细胞而形成软骨细胞—Pluronic F-127凝胶复合物。

The effects of safener on the growth and ALS activity were also examined. It showed that low concentration of AE F107892 could stimulate the growth of s-18 cultivars, but had little effect on the r-6 cultivars. High concentration of AE F107892 could inhibit the growth of both of the two cultivars.

测定了安全剂对小麦生长及ALS活力、GSH含量和GST活性的影响,结果表明:低浓度安全剂刺激敏18号小麦的生长,对抗6号的影响则较小,高浓度则都抑制了小麦幼苗的生长。

The results showed that the fractions of alcohol-benzene soluble and water soluble decreased with the process of decomposition. The concentration of semicellulose and cellulose increased firstly and then decreased. However, the concentration of lignin increased.

结果显示,随着腐解进行,腐解产物中的苯–醇溶性、水溶性组分下降,半纤维素和纤维素含量先上升后下降,而木质素增加;腐解物的能态呈现上下起伏、下降和相对稳定3个阶段的变化,总体是一个放能过程。

Separata was significant under the concentration of over 1.00 mgmL^(-1), and showed dosage-dependant pattern. The highest antifeedant rate was 65.68 %. Which concentration is within 0.25~1.00 mgmL^(-1), the feed intake of the 4th instar larvae of M.

浓度大于1.00mgmL^(-1)的羟基马桑毒素对3龄粘虫幼虫有明显的拒食作用,且随着药剂浓度的增大,拒食作用增强,最大拒食率达65.68环。

Under the condition of different chitosan concentration, pH and temperatures, adopt the spectrophotography to measure adsorb after the concentration of the dye, got the best condition of adsorb of chitosan to dye, result is:The amount of devotion of the chitosan is within the scope of the red 3B are 2%, blue 2BG and yellow 3GE are 3%, pH8.4 at alkaline, the temperature is the best for 50℃.

在不同的壳聚糖浓度、 pH 和温度条件下,采用分光光度法测得吸附后染料的浓度,得到了壳聚糖对染料的最佳吸附条件,结果为:壳聚糖的投入量在红3B 为2%,兰2BG 和黄3GE 为3%时, pH8.4在碱性范围内,温度为50℃效果最佳。

Results The mortality rate of mice in 80 mg/kg, day cyclophosphamide group was 16.7%, and T level [ at 30th day :( 1.38 ± 0.31 );45th day:( 1.15 ± 0.26 ) ] and T/LH ratio [ at 30th day:(0.163 ± 0.014); 45th day:(0.127 ± 0.023 ) ] were significantly decreased (all P<0.05) at 30th day after induction;The concentration of MDA [at 15th day:(2.70 ± 0.41);30th day:(2.710.36);45th day:(2.67 ±0.43) ] was maintained at a high level (all P<0.05) during the 45 days ; Number of Leydig's cells [ at 15th day:(9.65 ± 0.75 ); 30th day:( 14.05 ± 0.67 ); 45th day:(8.49 ± 072)] and layers of spermatogenetic epithelia [ at 15th day:(4.75 ± 0.82);30th day:(3.60 ± 0.49);45th day:(3.74 ± 0.43 ) ] were significantly decreased ( all P < 0.01 ) and stabilized in a low level. The induced model was stable and the mortality rate was acceptable. In the 60 mg/kg, day cyelophosphamide group, the T level and T/LH ratio had no significant change (P > 0.05 ), and the concentration of MDA ,number of Leydig' s cell and layers of spermatogenetic epithelia recovered at 30th day after induction. The induced model was unstable.

结果 剂量每日为80 mg/kg体重小鼠成模后死亡率为16.7%,血清T[30 d:(1.38±0.31);45 d:(1.15±0.26)]及T/LH比值[30 d:(0.163±0.014);45 d:(0.127±0.023)]于诱导后第30天出现显著下降(P均<0.05),而诱导后睾丸组织内MDA含量[15 d:(2.70±0.41);30 d(2.71±0.36);45 d:(2.67±0.43)]维持高水平(P均<0.05),生精上皮层次[15 d:(4.75±0.82);30 d:(3.60±0.49);45 d:(3.74±0.43)]和间质细胞[15 d:(9.65±0.75);30 d:(14.05±0.67);45 d:(8.49±0.72)]均显著减少(P均<0.01)并稳定于低水平,模型稳定,死亡率适当;每日60mg/kg体重组小鼠血清T及T/LH比值于不同时段并未出现明显变化(P>0.05),且睾丸组织内MDA含量、生精上皮层次和间质细胞计数在30 d后有所恢复,模型不稳定;每日100 rag/ks体重组死亡率为30.0%,死亡率过高。

There exists the optimum technical parameters about the effects of hydrolysis conditions. When the concentration of H+is 2.6 2.8 mol/L, the concentration of TiOSO4 is 25 28 g/L, the time of hydrolyzation is 60 min and the temperature of hydrolyzation is 125℃respectively, the yield of TiOSO4reaches 95%, the particle size of H3TiO3 is less than 40 nm, and the powder of H3TiO3 is spheral.

研究结果表明:水解条件直接影响偏钛酸的粒径及其分布,其中,钛液酸度的影响最大;水解条件对TiOSO4水解率和偏钛酸粒径的影响存在着最佳结合点,即当c为2.6~2.8 mol/L,ρ(TiOSO4)(按TiO2计)为25~28 g/L,水解时间为60 min,水解温度为125℃时, TiOSO4的水解率可达95%以上,得到的偏钛酸呈球形且粒径为40 nm。

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