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by the hour相关的网络例句

查询词典 by the hour

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

Methods 50 nude rats were submitted to intraperitoneal injection of HO-8910 cells.After 14 days,these rats was distributed according to different procedures:(1)Control group.(2)Midline laparotomy(ML,consisting in bowel exteriorization on a mesh for 1 hour following xyphopubic laparotomy).(3)Gasless laparoscopy(GL,consisting in abodominal wall expansion by a NO.14 Forley catheter for 1 hour).(4)CO2 laparoscopy(CO2 L,pneumoperitoneum with CO2 at a pressure of 2 mm Hg for 1 hour).(5)He laparoscopy(HeL,the same as CO2L except for inhalation with He).

50只裸鼠腹腔内注射卵巢癌HO-8910细胞,于14天后按不同手术要求分组如下:(1)对照组;(2)开腹组(ML,耻骨联合上正中切口长约2 cm进腹,将肠管等脏器取出搁置在无菌盐纱上,手术持续1 h);(3)气囊组(GL,腹腔内置14号Forley导尿管1根,充气后持续膨腹1 h);(4)CO2气腹组(CO2L,剑突下气腹针穿刺进腹充入CO2,压力维持在2 mm Hg,持续注入1 h);(5)He气腹组(HeL,手术步骤均同CO2气腹,仅注入气体为He)。

Establishment of man-hour quota for mould design based on analogism;2. A universal system of computer-aided man-hour quota ,based on primitives theory,is proposed,in which man-hour quota is constituted according to the data obtained by work study method in workshop and the rule of man-hour variety is studied by neural network.

提出了一种基于基元理论,以工作研究法现场测定数据作为制定定额的依据,运用神经网络研究工时变化规律的通用化计算机辅助工时定额系统,在此基础上探讨了工时的分类划分,阐明了系统的体系结构和功能模块,最后介绍了系统的应用流程。

Through researching the mechanism of biological nitrification and denitrification and actual project application of the technology and related literature materials, the obtained results are as follows:(1) Anoxybiosis is effective to the removal of COD; after the anoxic process, BOD/COD of the outflow increases, it shows that the degradation ability of wastewater is improved; anoxybiosis is insensitive when shock loading of inflow wastewater varies greatly;(2) It is demonstrated by the operation of inoculation and cultivating that biofilm takes two weeks to succeed in cultivating on packings and the removal ratios of NH3-N and COD get 50% and 70% respectively, when gas-water ratio is 6:1, HRT is 7.3 hour, water temperature is above 15°C;(3) It is demonstrated that gas-water ratio, hydraulic loading, HRT, temperature, pH etc are important factors which influence the removal effect of pollutants, when the gas-water ratio is 6:1, hydraulic loading is about 0.38kgNH3-N/m~3.d, water temperature ranges from 15°C to 27°C, pH ranges from 7.5 to 8.0, the BIOFOR removal effect of pollutants is the best;(4) The operation indicated that, this technology has strong ability of nitrification and denitrification; it has extremely vital significance for reducing the water body eutrophication;(5) It is confirmed the feasibility and the usability of preanoxic-BIOFOR process to treat L-lactic acid production wastewater. The experiment indicated that the treatment effect of this technology is very good and also shows that the technology has many advantages, such as small volume, high treatment efficiency, good effluent quality and strong endurance to load variation, this technology is a new and economical wastewater treatment process.

通过对生物脱氮机理的研究和该组合技术的实际工程应用,并结合有关文献资料,取得如下结论:(1)预缺氧池对L-乳酸生产废水中的COD去除具有一定的效果;废水中难降解的高分子物质经过缺氧工段分解为易于氧化降解的物质,浮状有机物在水解菌的作用下,将不溶性有机物水解为溶解性物质;预缺氧池具有较强的抗冲击负荷能力;(2)BIOFOR接种挂膜过程表明:HRT为7.3h、气水比为6:1、水温保持在15℃以上,经过半个月生物膜即以形成,NH_3-N和COD的去除率分别达到50%和70%左右;(3)研究表明:气水比、水力负荷、HRT、温度、pH等是影响污染物去除效率的重要因素,在气水比为6:1,NH_3-N容积负荷为0.38kgNH_3-N/m~3·d,温度在15℃-27℃,pH在7.5-8.0之间的条件下,BIOFOR对污染物的去除效率达到最佳;(4)运行表明,该组合技术具有较强的脱氮能力,对于减少水体富营养化具有十分重要的意义;(5)经过半年多实际工程的现场调试与运行,验证了利用预缺氧—BIOFOR组合工艺处理L—乳酸生产废水的可行性和实用性,得出该组合技术具有占地面积小,处理效果好,运行费用省,耐冲击负荷能力强等优点,是一项新型、经济的污水处理技术。

Egr-1 mRNA and Egr-1 protein hadn't been found in the normal vein. The expressions of Egr-1 mRNA and Egr-1 protein had biphasic changes. By reverse transcription-PCR and in situ hybridization, we found that the level of Egr-1 mRNA rose at 1 hour after graft, the expression of Egr-1 mRNA was (35±7)%. Decline at hour 6, 24 and day 3, the positive rates of Egr-1 mRNA were (8±2)%,(8±6)% and (8±4)% respectively. Reincrease at day 7, a peak at day 28, the positive rate of Egr-1 mRNA was (45±6)%(compared with other phase, P<0.01). At day 42, the expression of Egr-1 mRNA declined again. Immunohistochemical staining and Western blot revealed Egr-1 protein had expressed at hour 2 early phase, the expression of Egr-1 protein was (30±5)%, and until to hour 6. The level of Egr-1 protein was decrease at hour 24 and day 3, the positive rates were (7±3)% and (7±8)% respectively.

结果 自体静脉移植后,Egr-1 mRNA和Egr-1蛋白的表达呈双相变化,即移植后1 h, Egr-1 mRNA表达迅速升高,阳性率为(35±7)%,6 h、24 h及3 d时下降到较低水平,阳性率分别为(8±2)%、(8±6)%和(8±4)%,7 d时又再升高,28 d时达高峰,阳性率为(45±6)%,此与其余各时点比较差异均有统计学意义(P<0.01),42 d时,Egr-1 mRNA的表达再次下降;移植早期(2 h)即有Egr-1蛋白的表达,阳性率为(30±5)%,并持续至6 h,24 h~3 d表达下降到较低水平,阳性率分别为(7±3)%和(7±8)%,7 d时又再升高,至移植后28 d,Egr-1蛋白的表达阳性率达到高峰,为(40±9)%,此与其余各时点比较差异有统计学意义(P<0.01)。

Soaraway completely automatic clean ball machine: Four the silk pair the ball completely automatic clean ball's machine performance is as follows, voltage: 380V(220V) power power source, power: 1.5(2.2)kw, installs the silk: 4(6) 2(3) ball, divides the ball way: The completely automatic electricity fuse is divided the ball way, the characteristic: The completely automatic operating mode, uses the most advanced guide block, will protect the tinsel the surface not by the abrasion, will cause the tinsel surface not to have the gloss rustily, will produce the product flower even, will be bright, is artistic, output for each hour 8(10)kg about.

腾飞全自动清洁球机:四丝双球全自动清洁球机的性能如下,电压: 380V(220V)动力电源,功率:1.5(2.2)kw,装丝:4(6)丝2(3)球,分球方式:全自动电熔断分球方式,特点:全自动操作方式,采用最先进的导丝器,保护金属丝的表面不会被刮伤,造成金属丝表面生锈没有光泽,生产出来的产品花型均匀、明亮、美观,产量为每小时8(10)kg左右。

Pristine Li-Al LDHs are synthesized by hydrothermal process in different reaction conditions by varying the aging time for 1 and 24 hours. Both the Li-Al layered double hydroxides (abbreviated as Li-Al LDH1 and Li-Al LDH24 for aging time 1 hour and 24 hours, respectively) were modified by using sulphanilic acid sodium salt hydrate, modified agent to form modified Li-Al LDH1-SAS and Li-Al LDH24-SAS. The morphology of the pristine layered double hydroxides are investigated by using wide angle X-rays diffraction, scanning electron microscopy and particle size analyzer which indicates that the crystallinity and aspect ratio is increased with increasing the aging time from 1 hour to 24 hours. The particle size of Li-Al LDH24 and Li-Al LDH1 are found to be ~1000 nm and ~250 nm, respectively. Both the pristine and modified LDHs are characterized by XRD, FTIR spectra and thermogravimetric analysis.

本研究目的在於改变长晶时间的长短,合成出同径大小的Li-Al LDHs,再经由改质剂sulphanilic acid sodium salt hydrate将Li-Al LDHs无机层材表面有机官能化制备出改质型Li-Al LDHs-SAS,於是进一步藉由扫描式电子显微镜、射径仪和穿透式电子显微镜等仪器分别观察LDHs改质前和改质后其主层结构型态上的变化;从中可以发现Li-Al LDHs随著长晶时间的增加其径有随之增大的趋势,但经有机化改质后其径会由於改质环境的影响明显低许多,针对此现象本实验将未改质和改质后之Li-Al人工无机层材制备成复材进一步探讨其在热性质和难燃特性上的为表现。

The sepsis model was established by Cecal ligation and puncture in mice. Thirty male BALB/c mice were randomly divided into five groups: sham operation group, the twelfth hour, twenty-forth hour, thirty-sixth and forty-eighth hour group after CLP.

采用盲肠结扎穿孔术建立脓毒症BALB/c小鼠模型。30只小鼠随机分为5组,分别为假手术组,CLP后12、24、36、48 h组,其中假手术组小鼠在假手术后24 h取标本检测作为对照组,其余四组小鼠分别在CLP术后的12 h、24 h、36 h和48 h取标本待检。

Sowe selected the colchicine optimum parameters were 0.6μg/ml and 6 hour culturedduration.The second, there were no significantly differences between the four groupsin 2 hour groups; and there were significantly differences between 0.2μg/ml groups and other three groups in 4 hour groups; and there were no significantlydifferences between the four groups in 6 hour groups; and there were significantlydifferences between 0.4μg/ml groups and other three groups in 8 hour groups onthe metaphases (P<0.05), in the experiment of the effect on the mouse 8-cellembryo stage single blastomere of colchicine with different concentrations andduration by x~2 statistical analysis.

根据实验的实际情况,适宜制备小鼠4-细胞期胚胎单卵裂球染色体标本的秋水仙素的处理浓度和时间是0.6μg/ml和6小时。2、在确定秋水仙素不同处理浓度和时间对小鼠8-细胞期胚胎单卵裂球中期分裂相数影响的实验中,经统计分析,阻断培养2小时组中四个浓度组差异均不显著;阻断培养4小时组中0.2μg/ml浓度组与其他三组差异显著;阻断培养6小时组中四个浓度组差异均不显著;阻断培养8小时组中0.4μg/ml浓度组与其他三组差异显著(P<0.05)。

So we selected thevinblastine optimum parameters were 0.1μg/ml and 8 hour cultured duration.The fourth, there were significantly differences percent between 10 hourgroups and other three groups in 0.1μg/ml groups; and there were no significantlydifferences between 8 hour groups and 10 hour groups, but they had significantlydifferences among other two groups in 0.3μg/ml groups; and there weresignificantly differences between 10 hour groups and other three hour groups in0.5μg/ml groups; and there were significantly differences between 10 hour groupsand other three groups in 0.7μg/ml groups on the metaphases (P<0.05), in theexperiment of the effect on the mouse 8- cell embryo stage single blastomere ofvinblastine with different concentrations and duration, by x~2 statistical analysis.

根据实验的实际情况,适宜制备小鼠4-细胞期胚胎单卵裂球染色体标本的长春花碱的处理浓度和时间是0.1μg/ml和8小时。4、在确定长春花碱不同处理浓度和时间对小鼠8-细胞期胚胎单卵裂球中期分裂相数影响的实验中,经统计分析,阻断培养0.1μg/ml浓度组中10小时组与其他三组差异显著;阻断培养0.3μg/ml浓度组中8小时组和10小时组间差异不显著,但与其他两组差异显著;阻断培养0.5μg/ml浓度组中10小时组与其他三组差异显著;阻断培养0.7μg/ml浓度组中10小时组与其他三组差异显著(P<0.05)。

So we selected the colchicine optimumparameters were 0.2μg/ml and 6 hour cultured duration.The third, there were significantly differences percent between 10 hourgroups and other three groups (4 hour groups, 6 hour groups and 8 hour groups) in0.1μg/ml groups; and there were significantly differences between 8 hour groupsand 10 hour groups, but they had no significantly differences among other twogroups in 0.3μg/ml groups; and there were significantly differences between 10hour groups and 6 hour groups, but 10 hour groups had no significantlydifferences among other two groups in 0.5μg/ml groups; and there weresignificantly differences between 8 hour groups and other three groups in0.7μg/ml groups on the metaphases (P<0.05), in the experiment of the effect onthe mouse 4- cell embryo stage single blastomere of vinblastine with differentconcentrations and duration, by x~2 statistical analysis.

根据实验的实际情况,适宜制备小鼠8-细胞期胚胎单卵裂球染色体标本的秋水仙素的处理浓度和时间是0.2μg/ml和6小时。3、在确定长春花碱不同处理浓度和时间对小鼠4-细胞期胚胎单卵裂球中期分裂相数影响的实验中,经统计分析,阻断培养0.1μg/ml浓度组中10小时组与其他三组差异显著(4小时组、6小时组和8小时组);阻断培养0.3μg/ml浓度组中8小时组和10小时组间差异不显著,但与其他两组差异显著;阻断培养0.5μg/ml浓度组中10小时组与6小时组差异不显著,而与其他两组差异显著;阻断培养0.7μg/ml浓度组中8小时组与其他三组差异显著(P<0.05)。

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