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2Predialysis plasma FC concentration in dialyzed patients was much lower than that in normal subjects and undialyzed patients(P.01),postdialysis plasma FC concentration was significantly lower than predialysis concentration(P.001). There was a 70%decline in plasma FC concentration during one hemodialysis session.

2尿毒症血透患者透前血浆FC浓度明显低于正常人和保守治疗患者(P.01),透后浓度显著低于透前(P.001);一次血透后浓度下降70%。

The specific gravity of degassed and undistilled beer sample plus real extract solution are determined in this method.The results of alcohol,real extract,original extract and real degree of attenuation etc.can be shown through the running of software program.

摘 要:通过测定脱气而不蒸馏的啤酒样品及浸出物溶液的比重,在开发的软件程序上运行后可得出酒精度、真正浓度、原麦汁浓度及真正发酵度等参数结果,该方法不需额外实验室硬件投入,比GB4928—91标准中蒸馏法测酒精度及原麦汁浓度含量提高效率8倍。

Compared of the efficiency of treating heavy metals in FGD wastewater with NaOH, Ca_2 and Mg_2. It indicated that NaOH was much efficient for precipitated waste water; Ca_2 was much efficient for unprecipitated waste water, the removal efficiency reached 98.4%. With the increasing of the main ion of Ca~2+, Cl~- in FGD wastewater, the efficiency decreased. It decreased 60% for the removing of Mn and 10% for Zn, Cd and Ni. The rectification coefficient token the Ksp of practical wastewater because it quite different with theoretic Ksp at different pH; the theoretic and practice addition were proportioned and it commonly reached 1:300.The precipitation efficiency of Na2S at different pH and the effect of Ca2+ was determined.

比较了NaOH、Ca_2和Mg_2处理脱硫废水时重金属的去除效果,分析了Ca~(2+)、SO_4~(2-)和Cl~-等主要离子的影响,结果表明:NaOH和Ca_2能有效处理脱硫废水中的重金属;对澄清废水而言,NaOH效果较好,对于未澄清废水而言,Ca_2效果更好,但去除废水中重金属的效率都能达到98.4%;随着Ca~(2+)、Cl~-等主要离子浓度的增大,中和作用去除重金属的效率降低,Mn最大降低60%,Zn,Cd,Ni降低10%左右;实际重金属浓度和用理论Ksp计算所得值差别很大,通过校正系数能有效计算实际重金属浓度;实现相同pH时氢氧化物的理论和实际投加量成一定比例,最大可达1:500。

The results showed that elevated CO2 increased the R/S ratio and the dry mass of both coarse and fine roots, indicating that the seedlings under elevated CO2 allocated more biomass to their belowground part. Compared with control, elevated CO2 increased the contents of reducing sugar, sucrose, and total soluble sugar in coarse roots significantly, but had less effect on those in fine roots. Elevated CO2 increased the contents of starch and total non-structural carbohydrate both in coarse roots and in fine roots. Under elevated CO2, the carbon content in coarse and fine roots had an unsignificant increasing trend, while the nitrogen content decreased significantly, which resulted in an increase of C/N ratio.

结果表明:CO2浓度升高使红桦幼苗粗根和细根的干质量增加,同时根/冠值显著升高,表明CO2浓度升高使红桦幼苗生物量向根系的分配增加;与对照相比,粗根的还原糖、蔗糖和总可溶性糖含量显著增加,而在细根中没有显著变化;粗根、细根的淀粉和总的非结构性碳水化合物含量显著增加;CO2浓度升高下粗根和细根的碳含量有升高的趋势但未达到显著水平,同时氮含量降低,碳/氮值升高;氮的吸收量在粗根和细根中均无显著变化。

The results showed that elevated CO2 increased the R/S ratio and the dry mass of both coarse and fine roots, indicating that the seedlings under elevated CO2 allocated more biomass to their below- ground part. Compared with control, elevated CO2 increased the contents of reducing sugar, sucrose, and total soluble sugar in coarse roots significantly, but had less effect on those in fine roots. Elevated CO2 increased the contents of starch and total non-structural carbohydrate both in coarse roots and in fine roots. Under elevated CO2, the carbon content in coarse and fine roots had an unsignificant increasing trend, while the nitrogen content decreased signifi- cantly, which resulted in an increase of C/N ratio.

结果表明:CO2浓度升高使红桦幼苗粗根和细根的干质量增加,同时根/冠值显著升高,表明CO2浓度升高使红桦幼苗生物量向根系的分配增加;与对照相比,粗根的还原糖、蔗糖和总可溶性糖含量显著增加,而在细根中没有显著变化;粗根、细根的淀粉和总的非结构性碳水化合物含量显著增加;CO2浓度升高下粗根和细根的碳含量有升高的趋势但未达到显著水平,同时氮含量降低,碳/氮值升高;氮的吸收量在粗根和细根中均无显著变化。

Results Using different concentrations of 5fluorouracil to deal with A549 cells, with the increase in drug concentration and treatment time,cell survival rate decreased significantly;and low concentration of 5fluorouracil induced the cell spread and increased vacuolization within the cytoplasm, acridine orange staining showed an increase in acidic vesicles,high concentration made the cell round and cell apoptosis.

结果不同浓度的5氟尿嘧啶处理A549细胞,随着药物浓度的增加和处理时间的延长,细胞存活率明显下降;且低浓度使细胞呈铺展状态,细胞质内空泡增多,吖啶橙染色显示酸性膜泡增多,高浓度使细胞变圆,出现凋亡状态。

The fluorescent intensity ratio of the first vibronic peak (λ=373 nm) to the third vibronic peak (λ=383 nm) of pyrene solubilized in micelle decreased gradually, which was different from the conventional surfactant, such as SDS. The aberrant property indicated a broad micelle size for the m+nAr-T surfactants. That is, the aggregates of the studied surfactants gradually grew in size with increasing concentration over wide concentration range.

与传统表面活性剂不同,增溶于N-酰基牛磺酸钠胶团中的芘的第一个电子振动峰(λ=372nm)的荧光强度I1和第三个电子振动峰(λ=385nm)的荧光强度I3之比I1/I3值随着表面活性剂浓度的增加而缓慢降低,说明了N-酰基牛磺酸钠表面活性剂在低浓度区形成疏松的聚集体,随着浓度的增大则有更多的表面活性剂分子挤入已形成的聚集体。

Methods: hRPE were cultured in normal (95% oxygeon) and hypoxia (2%-5% oxygeon) condition with DEX of different concentrations. The influence of DEX on cells growth and VEGF expression was detected by 3-(4,5-dimethylthiazole-2yl)-2,5diphenyl tetrazolium bromid and reverse transcriptionassay.

体外正常(氧浓度95%)和缺氧(氧浓度2%~5%)下培养视网膜色素上皮细胞,分别加入不同浓度地塞米松,用四唑溴盐和RT-PCR的方法,分别检测药物对细胞生长的影响和细胞VEGF的表达。

The results were very successful.The removal rates of chromaticity and CODCr reached 96.56% and 94.46% respectively under the optimal conditions as follows:dosages of H2O2 and Fe2+ were 4.0g/L and 0.3 g/L respectively,microwave irradiation power was 500 W,and radiation time was 1 min.The investigation shows that the microwave irradiation,homogeneous Fenton oxid...

结果表明,微波-Fenton氧化-PASS混凝法适合于处理复杂垃圾渗滤液,在H2O2的质量浓度为4.0 g/L,Fe2+质量浓度为0.25 g/L,pH值为3.0,固定微波辐射功率500 W,辐照1 min,PASS质量浓度为25 mg/L的最佳条件下,出水色度仅15倍,脱色率和CODcr去除率分别达到96.86%和94.46%;微波辐射、Fenton氧化和PASS混凝沉淀结合处理垃圾渗滤液废水时具有较好的协同效应。

The sizes of the self-assembly micelles of the amphiphilic block copolymers and the effects werestudied by dynamic light scattering and UV-visible spectrophotometer. The micelle sizes werelargely influenced bythe hydrophobic chain content in the copolymer, the properties of the solvent and the copolymer concentration in the organic phase. The morphology of the micelles was investigated by transmission electron microscopy. Theresults showed that the micelles appeared spheres with inner core and outer shell. The critical association concentrations were determined by pyrene monomer fluorescence probe technology. The degradability of copolymer was studied by the loss of the intrinsic viscosity in the degradation process. The results indicated that the degradation rate of PECL was slower thanthat of PELLA and PEDLLA. The stability of the copolymer micelle dispersion was examined by measuring the critical flocculation concentration, which gradually decreased with increasing the content of thehydrophobic chain in the copolymer. The rheological results showed thatthe viscosity ofthe micelle dispersion with higher content of PEG segments was firstly decreased and then increased with the increasingthe temperature. Otherwise, the variation of viscosity was irregular. The viscosity of the micelle dispersion increased with the increase of the electrolyte (Na 2SO 4) concentrations. Polymer micelles paclitaxel was prepared by self-emulsification/solvent evaporation method and solid dispersion technique with amphiphilic block polymers as the carrier material.

运用动态光散射和紫外分光光度计研究了两亲性嵌段共聚物自组装胶束的粒径及其影响因素,结果表明,自组装胶束的形成机理受制备方式的控制,胶束的粒径随着共聚物相对分子质量或疏水嵌段相对分子质量和有机相中共聚物浓度的增大而增大,随着有机溶剂的水溶性的增强而减小;采用透射电镜观察胶束的形态结构,发现胶束呈具有核壳结构的均匀球形;采用芘荧光探针法测两亲性嵌段共聚物的临界聚集浓度;通过降解过程中共聚物特性粘度的变化研究两亲性共聚物的降解性能,发现与PELLA和PEDLLA的相比,PECL 降解速率较慢;随着共聚物中疏水嵌段含量的增大,纳米分散液的稳定性逐渐下降;PEG含量高的PEDLLA纳米分散液随着温度的升高,纳米分散液的粘度先下降然后增大,反之,没有规律性,且随着电解质Na 2SO 4浓度的增大,体系粘度增大。

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