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normal room
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  普通房间
     Comparison between Evaluation and Experiment for Placements of Subwoofer in a Normal Room
     普通房间中辅助低频扬声器箱摆位的理论计算与实验对比
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     In this paper a numerical modal of VSB system which has a three-dimensional structure is investigated. It can generate a quiet zone of a human head size in a normal room where the noise comes from many different directions.
     本文建立立体结构的VSB系统模型,从数值模拟和实验两方面说明在噪声来自于多个方向的普通房间中,通过该系统产生人头大小的静区是可行的。
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  “normal room”译为未确定词的双语例句
     normal room air with TA: 137.1±10.2;
     正常加药组的A值为137.1±10.2;
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     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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     Based on the results of monitoring the inhalable particulate matter(PM10) and the total suspension particulate(TSP) in room air,the pollution state of inhalable particulate matter in normal room and the effects of dwelling environment on the indoor PM10 concentration are analyzed,the relationship between the concentration of PM10 and TSP in air is also studied.
     通过对居室空气中可吸入颗粒物(PM10)及总悬浮颗粒物(TSP)监测,应用监测结果分析了一般居室污染中可吸入颗粒物的污染情况及居住环境对室内PM10浓度的影响,同时研究了空气中PM10浓度与TSP浓度的关系。
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     Calculation & Recommendation of Design Dimension of Mine Block Structure Main Parameters Involving Normal Room-pillar Method
     普通房柱法矿块结构参数的计算及设计尺寸推荐
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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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     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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     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。
短句来源
     and 6. normal.
     6.正常型。
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     My Room
     我的房间
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     room temperature.
     温度:室温。
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  normal room
The coatings were tribologically tested in a pin-on-disk apparatus with increasing applied normal loads in two different environmental conditions, normal room atmosphere and dry nitrogen atmosphere.
      
Our hypothesis is that the surface reactivity of polished bioactive glass slides might decrease slowly due to the influence of (air-) humidity during storage under normal room conditions.
      
The method was established by overnight exposure of the fiberscope to the gas at room temperature and pressure, or by a 30-minute exposure to the gas at 60°C and normal room pressure.
      
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.
      
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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 optimum...

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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