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Needle taking place is commonly used the rescue that changes cure and danger to weigh a patient at patient of children, tumour, in infusion, because secure not firm outside can bringing about syringe needle slippery haemorrhage to be in charge of, cause local strut, aching, serious person can send infiltration of the certain pharmaceuticals that change cure to cause subcutaneous tissue hypodermically necrotic or the liquid cannot be defeated in time note and illness of incur loss through delay, new puncture increases the patient's anguish not only, also increased economic burden to also can be affected at the same time to the patient nurse working quality, the course relapses clinical experiment, my division adopts vein to accept the annular and fixed method of buy needle, obtained better result, introduce as follows now. 1 method is taken fixed stick (needle taking place is deployed) together, the disinfection that wide 10cm controls wraps cloth, two paragraphs of end are seamed on after sticking glue to buckle vein to leave buy needle puncture to succeed, convention is secured with adhesive plaster, next the ground degree of tightness will take stalk of handle of buy pinhead, needle, needle to be in firmly aptly fixed and fixed stick , next annular in blood-vessel twine stick on stick buckle. 2 experience apply this method to secure vein to left buy needle method to reduce the patient's anguish, reduced cost, provided mobile space for the patient, also avoid heparin cap prolapse, still facilitate observation puncture is nodded, do not affect hematic use, gauze pad can alleviate heparin cap is oppressive and unwell, reduce infusion pollution.

概要: 留置针常用于小儿、肿瘤患者化疗及危重患者的抢救,在输液中,由于固定不牢可导致针头滑出血管外,引起局部肿胀,疼痛,严重者可致某些化疗药物渗入皮下造成皮下组织坏死或液体不能及时输注而延误病情,重新穿刺不仅增加病人的痛苦,也给病人增加了经济负担同时也会影响护理工作质量,经过反复临床实验,我科采取静脉留置针的环形固定方法,取得了较好的效果,现介绍如下。1方法取固定贴一块,宽10cm左右的消毒包布,两段端缝上粘胶扣静脉留置针穿刺成功后,常规用胶布固定,然后将根据松紧适宜将留置针头、针柄、针梗处牢牢固定固定贴,然后在血管中环形缠绕粘上粘扣。2心得应用此方法固定静脉留置针方法减少了患者的痛苦,降低了费用,为患者提供了活动的空间,也避免肝素帽脱垂,还便于观察穿刺点,不影响血运,纱布衬垫可缓解肝素帽压迫不适,减少输液污染。

There are three platinum catalyst micro channels which have different width ,such as 1000 m , 400m and 40m. The platinum catalyst micro channel reactor is fabricated by MEMS technology. The reactor uses the exothermic reaction of hydrogen and oxygen on the platinum catalyst plate as the heat source and the platinum thin film resistance deposited on a glass chip by face micro machining process as catalyst and temperature sensor. The channel is bonded with a cover plate etched by bulk micromachining technology to become a mico- channel reactor.

实验主要以微机电加工技术制作白金触媒微管道反应系统,利用微机电面型加工技术将白金薄膜电阻制作於基材为玻璃的晶片上,以此为反应所需的触媒及温度量测元件,并用体型加工技术蚀刻出微流道的上盖板相结合成微管道反应系统,本研究以1000μm、400μm及40μm的白金触媒微管进行测试,并利用微管道管壁上触媒表面降低反应活化能的特性来维持反应,此微反应系统利用氢气与氧气在白金触媒平板上的放热反应作为能量的来源。

A computer-aided local transient flow property measuring system was developed using a high speed CCD camera coupled with optical fibers in order to study the Gas-liquid-solid three-phase jet loop reactors. SnO2 crystal films were orientally deposited on the alkoxysilane molecule-coated hydroxyl glass substrates so as to prepare surface-marked particles as the tracers. An image analysis system was established to identify different phases. Stroboscopic photography was utilized to extend the measure range. The developed measuring and analysis system was capable of determining accurately the local transient flow property in a G-L-S jet loop reactor. Based on the above system, local transient flow properties of gas, liquid, and solid phase were measured and studied the influences of fluid property, operation and configuration parameters on the reactor.

中文摘要:以气液固三相喷射环流反应器为研究对象,将高速CCD和光纤束耦合制成局部瞬态流动特性微机数据采集及图象处理系统,利用MPS硅烷分子在带有羟基的玻璃基底上的自组装引导SnO2晶态膜层在功能化表面上进行沉积,以获得表面标记的示踪粒子,解决图象处理技术与相的识别的问题,利用频闪技术拓展了测量上限,得到可以准确测定气液固三相喷射环流反应器中局部瞬态流动特性的测试系统;采用上述测试技术进行喷射环流反应器中局部气相、液相与固相瞬态流动特性的实验研究,并考察物性参数、操作参数与结构参数的影响规律。

The fatter mice in Gewirtz's study had been bred to lack a protein known as toll-like receptor 5 (TLR5), which most intestinal cells sprout on their surface. Its job is to recognize and bind to the whiplike flagella that bacteria use to move around. TLR5 acts as a traffic cop for controlling the mass of pathogens living in the intestine; without it, the normally harmless gut bacteria tend to overflourish and expand in number. See and listen to an audio slideshow about obesity rehab.

Gewirtz 实验中的胖小鼠普遍缺乏一种被称之为 toll 样受体5 (TLR5)的蛋白,这种蛋白是肠上皮细胞表面分泌的, TLR5的作用是识别并结合在肠道细菌的运动器官鞭毛上,在对大多数肠道病原体的控制中, TLR5扮演着交通警察的角色,没有它,一般无害的肠道菌就会异常活跃并且大量繁殖。

After carefully analyzed the principle of standard SVPWM and traditional overmodulation methods, this paper proposed one simple and effective overmodulation scheme. Experiments were carried out in one 1.5kW induction motor and its results were recorded and analyzed by PZ4000 Power Analyzer and the proposed scheme were proved to be effective.

在分析了标准SVPWM算法和常见各种过调算法的原理的基础上,提出了一种简单有效的算法满足过调控制的要求,在1.5kW异步电机上进行了实验并使用PZ4000功率分析仪对其结果进行了准确测量与分析,证明了本文提出的SVPWM算法可以有效地提高电源电压的利用率。

In view of the theory and practice, multi-channel mode-filtered light CE has potentials in chiral separation of the biomolecules and the pharmic molecules, and in study of biological characteristics of the interaction of the bio-molecules with the pharmic molecules.

从理论和实验两方面来看,我们期望多通道模式滤光CE在生物分子和药物分子的手性拆分上、在研究生物大分子和药物分子之间相互作用的生物特征上,可以获得良好的应用。

Wang Zhe'nan stealed my several RMB then stealed tens thousand RMB of my family's,poured oil onto my trousers,a student of Beijing university,he put poisonous drugs which can do harm to my eyes' slight in order to test the reason why his eyes' slight has been lower than before and its effect,put Hg in the medicine of the program of cleaning teeth,scalding oil harmed my nose,the serious issues they didn't allow me to write,he and Bi Yue wrote strange symbols in my books.

汪哲楠偷走我几元钱又偷走我家几万元,把油泼到我的裤子上,北京大学学生,拿我做对视力破坏的毒剂的实验研究他视力下降的原因以及影响,投入水银在洁牙项目,滚油烫我鼻子,严重的事件他们不让我写,他和毕玥等人在我书上乱画。

By using the developed software which is based on the commercial software PHOENICS 1.4, the distribution of Fe in laser molten pool in an experiment of cladding Stellite 6 on 12CrMoV is calculated.

利用在商业软件PHOENICS 1.4基础上开发的模拟软件,针对在12CrMoV钢基底上熔覆Stellite6合金计算了熔池中Fe的浓度分布,计算结果与实验结果大体相符。

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 different enzyme protecting agent had effected on the liquid alkaline protease under the dissimilar condition. Taking the living rate of enzyme as the target, we obtained one high effective alkaline protease stabilizing agent formula through orthogonal experiments as following: 5 mmolL^(-1) Ca(superscript 2+), 15mgmL^(-1) trimethylene glycol-single methyl ether, 0.015% 4-formyl phenyl-boron dihydroxide, 1% glycerine.

在此基础上,进行L13(3^7)正交实验,以相对酶活率为指标,考察了不同酶活性保护剂在不同条件下对液体碱性蛋白酶活力的影响,筛选到一种优质高效的碱性蛋白酶稳定剂配方为:5mmolL^(-1) Ca(上标 2+),15mgmL^(-1)丙二醇-单甲醚,0.015% 4-甲酰苯基硼酸,1%甘油。

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This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。