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normal room temperature
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  “normal room temperature”译为未确定词的双语例句
     The —NCO content is 10% in the prepolymer, the calcium carbonate and petroleum resin content is 15% and 30%, use MOCA/N-330 (function group) is 0.75/0.25 as the mixed curing agent, prepared the normal room temperature cure oily two component polyurethane waterproof coating.
     预聚体中的—NCO含量为10%,轻钙用量为总量的15%,石油树脂为总量的30%时,以MOCA/N-330(官能团)为0.75/0.25作为混合固化剂,可制得普通型室温固化油性双组分聚氨酯防水涂料。
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     Microwave processing condition was low power for 60min after boiling at high powder, and time of sugar-dipping was Shours in normal room temperature.
     微波处理条件为:高火煮沸后低火煮制60min; 常温 渗糖5h;
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     The results show that better extraction effect can be got by using 0.5-1 % citric acid solution for extraction solution and 95 % alcohol for elution solution at normal room temperature.
     结果表明:在常温下以0.5~1%的柠檬酸为提取剂,95%的乙醇为洗脱剂,能达到很好的提取效果.
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     Using a lab constant potential method to determine anodic stead polarization curves,the authors systematically studied electrochemical corrosion reaction of titanium alloys applied to biomedicine,such as T42NG titanium alloys bimetals,which were compounded by 3Cr13 stainless steels,at normal room temperature and air pressure,in the 3.5% NaCl water solution.
     对生物医用的T42NG经3Cr13不锈钢复合构成的T42NG钛合金"双金属材料",在常温常常压下3 5%的NaCl水溶液中,采用"三电极体系"实验装置运用恒电位法测定其阳极稳态极化曲线,对其电化学腐蚀行为进行了系统地研究。
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     Otto buffers is simpler in components,and lower in cost than Marie's buffer,also it can be analyzed and conserved under normal room temperature conditions.
     其中Otto buffers的组分较Marie’s nuclear isolation buffer简单、成本低,且能在正常室温条件下分析和保存。
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     Patients in normal temperature group were treated at the room temperature.
     常温组患者在室温下对症处理。
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     The Relation Coordination in the Piano Room Management of Normal Colleges
     高师琴房管理中的关系协调
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     Room for maintaining normal school teaching is the basic work.
     机房维护是保证学校进行正常教学活动的基础工作。
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     architecture as normal
     建筑如常
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     Chat Room
     本刊聊天室
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  normal room temperature
The results suggest that embryos can be preserved with a little loss of viability in the presence of ABA even at the normal room temperature (25 + 1 °C) up to two years without any transfer.
      
The prills were stable at normal room temperature and RH.
      
This reduced pathogenicity was observed at normal room temperature where the baby mice had a body temperature of 32.5 °C, which is even below the permissive temperature for growth of the mutants.
      
A young healthy man, nearly nude and adapted to heavy work in heat, performed different physical work on a treadmill in 105 working experiments, each work session lasting 2 to 51/2 h in the morning after rest in bed in normal room temperature.
      
Results indicate that differences between suits that may be of little importance at normal room temperature become significant at higher stress levels (increased activity and/or air temperature).
      
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Fresh midgut tissue of the Densonucleosis larva was pounded to pieces in pH 7.2 phosphate buffer solution. Then clarifyied repeatedly with chloroform, and precipitated with ammonium sulphate,followed by centrifugation at a low speed 3 000 r/min and normal room temperature. The separated and purified virus had a maximum ultraviolet absorption at spectrum 260 nm. pure viral .particles in virus suspension were detected under electron microscope. A antiserum, which had a specific reaction pattern of titer...

Fresh midgut tissue of the Densonucleosis larva was pounded to pieces in pH 7.2 phosphate buffer solution. Then clarifyied repeatedly with chloroform, and precipitated with ammonium sulphate,followed by centrifugation at a low speed 3 000 r/min and normal room temperature. The separated and purified virus had a maximum ultraviolet absorption at spectrum 260 nm. pure viral .particles in virus suspension were detected under electron microscope. A antiserum, which had a specific reaction pattern of titer 1024 , was obtained from the antiserum prepared with the virus suspension.

剖取浓核病蚕的新鲜肠组织,在pH7.2的磷酸级冲液中捣碎,经用氯仿反复抽提澄清,硫酸铵盐析,结合3000r/min常温低速离心分离纯化本病毒,得到了紫外吸收高峰260nm、电镜观察病毒粒子纯净的病毒悬液,将此病毒液制备抗血清,得到了效价在1024特异性强的抗血清.用此抗血清对浓核的病蚕进行各种早期诊断时,免疫双扩散、对流免疫电泳法,一般在感染后24—36小时检出,间接荧光抗体法12—24小时就能检出.具有特异性强、灵敏度高、检出早的特点,在当前富有实用意义.

Through the contrast experiment, when using the eurcumin colorim-etric analysis to determine the effective boron of soil, the effects of every condition such as the quantity of soil, the amount of solution, the boiling time, the drying temperature, the colour showing time, the turcumin reagent solution storage time, the diameter of soil particles, and all the utensils on the determined results were found out. On the basis of these effects, we defined: when soil and water is in a ratio of one to two , the...

Through the contrast experiment, when using the eurcumin colorim-etric analysis to determine the effective boron of soil, the effects of every condition such as the quantity of soil, the amount of solution, the boiling time, the drying temperature, the colour showing time, the turcumin reagent solution storage time, the diameter of soil particles, and all the utensils on the determined results were found out. On the basis of these effects, we defined: when soil and water is in a ratio of one to two , the optimum condition of eurcumin colorimetric anal ysis are: the quantity of soil-20kg, the quantity of reagent solution-0.5 0.5-1 ml, the boiling time-10 minutes, the drying temperature-from 60° to 70°C, the colour showing time-from an instance to 120 minutes, the regent solution storage time-within3 days at normal room-temperature in dark place or within 10 days at 0°C in a refrigerator, the diameter of soil particles and the amount of effective boron contained tend to appear negative interrelated. The result doesn't have nota-ble difference when using polyvinyl chloride beaker instead of quartz beaker.

通过对比试验找出了用姜黄素比色法测定土壤中有效硼含量时,取土量和试液量、煮沸时间和蒸干温度、显色时间和姜黄素溶液存放时间、土壤粒径和所用器皿诸条件对测定结果的影响。据此确定了当土:水=1:2时用姜黄素比色法测定土壤有效硼含量的最佳条件为:取土量—20克,试液量—0.5~1.0毫升,煮沸时间—10分钟,蒸干温度—60℃—70℃,显色时间—从即时到120分钟以内,姜黄素溶液存放时间—室温暗处不超过3天,冰箱0℃左右不超过10天,土壤粒径与有效硼含量呈负相关趋势,用聚乙烯塑料烧杯替代石英烧杯结果无显著差异。

Results of laboratory experiments showed that soaking with warm solution of several biological agricultural antibiotics was an effective method of eliminating Erwinia stewartii pathogen carried in imported corn seeds. It was found that soaking the seeds for 1.5 hours in solutions of Xinzhimeisu 300 ppm, or Wuyijunsu 120 ppm, or Agricultural Antibiotic 120 at 1:20, or Zhongshengjunsu at 1:20, with the solution temperature changed from 47℃ to 40℃, was sufficient to destroy "the bacterium. This method could also...

Results of laboratory experiments showed that soaking with warm solution of several biological agricultural antibiotics was an effective method of eliminating Erwinia stewartii pathogen carried in imported corn seeds. It was found that soaking the seeds for 1.5 hours in solutions of Xinzhimeisu 300 ppm, or Wuyijunsu 120 ppm, or Agricultural Antibiotic 120 at 1:20, or Zhongshengjunsu at 1:20, with the solution temperature changed from 47℃ to 40℃, was sufficient to destroy "the bacterium. This method could also stimulate germination of the seeds. In comparison, soaking the seeds with the same antibiotics at normal room temperature did not eliminate the bacterium completely and required 18 hours for the treatment.

试验证明,抗菌剂变温浸种灭菌法是铲除潜伏在种子内部病原细菌的一种有效技术。采用新植霉素300ppm或武夷菌素120ppm、农抗“120”1:20,药温47℃,浸种1.5小时,均可获得彻底灭菌效果。并且对种子发芽有促进作用,发芽率比对照增加2.0~7.4%。常温抗菌剂浸种,浓度与变温浸种相同,而浸种时间需延长至18小时。其结果无论哪种抗菌剂处理均有病原细菌存活8.4×10~25×10~2CFU/ml。同时种子发芽率也有所下降。因此,常温浸种不能用于引种玉米的消毒处理。

 
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