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thermal analysis results
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  热分析结果
     The TG-DSC thermal analysis results showed the desired products decomposition point being generally at around 200 C ~ 300C, therefore they had goodthermal stability.
     对合成产物的TG-DSC热分析结果表明它们热分解点一般在200℃~300℃左右,具有较高的热稳定性。
短句来源
     Effect of Trace Elements on Thermal Analysis Results of AI-Si Alloys
     微量元素对Al-Si共晶合金热分析结果的影响
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     TG/DTA thermal analysis results indicated, while rising from room temperature to 400 °C with the heating rate of 3k/min and 8k/min respectively and kept the 400 °C temperature for lh, the total weight losses (that is hydrogen released) were all larger than 6.5%; the initial endothermic temperature were at 270 °C approximately and the endothermic peak were above 350°C.
     TG/DTA热分析结果表明,分别以3k/min和8k/min的速率由室温升温至400℃,并于400℃保温1h时,总失重(放氢量)都大于6.5%,吸热起始温度为270℃左右,吸热峰尖在350℃以上。
短句来源
     Thermal analysis results of β-chitin nanoparticles indicated that β-chitin is stable under 200 ℃ and decomposes gradually with the rise in temperature. Only a little residue remained when the temperature reached 700 ℃.
     热分析结果表明,β-甲壳质纳米颗粒在200℃以下是稳定的,随着温度的升高,β-甲壳质纳米颗粒逐步分解,700℃时只剩余少量灼烧残渣。
短句来源
     Meanwhile, the thermal analysis results indicated that the thermal stability of these ZnTiO3-based ceramics were enhanced by the increasing amount of cobalt substitution, and that cobalt substitution appeared more remarkably than nickel substitution.
     与此同时,热分析结果证实,伴随钛酸锌基陶瓷体系掺杂钴量的增加,其六方相的热稳定性提高,且效果比掺杂镍更加显著。
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     Thermal analysis results indicated formamidine disulfide di-hydrochloride exhibit complex behaviors from the curves of TG-DTA-DTG,firstly including two first order decomposition reactions and its apparent activation energy is 155.71 kJ/mol,36.12 kJ/mol.
     二硫甲脒盐酸盐的TG-DTA-DTG曲线说明,产物首先发生了两次一级分解反应,其表观活化能分别为155.71 kJ/mol和36.12 kJ/mo。 l
短句来源
     Thermal analysis results show that the catalytic action has close relations with diameter and specific area of Fe_2O_3 particles.
     结果表明,Fe2O3粒子对AP热分解的催化性能与其粒径及比表面积有很大关系。
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     It was indicated that Yb(NO 3) 3·6H 2O was fully decomposed into Yb 2O 3 above 460℃ at a heating rate 20℃/min. Based on the thermal analysis results,pure cubic phase Yb 2O 3 powders with uniform size of 0.50~1.50μm were prepared by spray pyrolysis from aqueous solution of Yb(NO 3) 3·6H 2O.
     在此基础上,以Yb(NO3)3·6H2O为前驱体采用喷雾热分解法制备出粒度为050~150μm的单相立方晶系球形Yb2O3粉末。
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     In this paper, the physico-chemical properties, infrared spectrum and differential thermal analysis results of anti-settling aluminate(ASA) have been reported(?)
     本文报导了防沉降性铝酸酯(Anti-Settling Alumjnate简称AsA)的理化性质、红外光谱和差热分析的结果。
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     Theresults showed that the dissolution from fast-release pellets was significantly increased when the ratio of 1-HPMCP-silicawas up to 1∶2∶2. The X-ray diffraction and differential thermal analysis results showed that the crystalline peak of 1 inboth pellets were disappeared, and there were no drug crystals on the surface of the pellets under scanning electron microscope.
     结果表明,当速释小丸中的尼群地平-HPMCP-微粉硅胶的比例达1∶2∶2以上时,溶出度迅速提高; X-射线衍射和差热分析结果表明速释和缓释小丸中药物结晶峰消失;
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  相似匹配句对
     Thermal Analysis of Ladle
     钢包的热分析
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     REVIEW OF THERMAL ANALYSIS
     热分析进展
短句来源
     Analysis of G.
     G.
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     C -- M. S analysis.
     —M. S.
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     Results:
     结果:
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  thermal analysis results
Structural, spectral, and thermal analysis results confirmed the presence of the solvents and differences in the structural properties of these solvates.
      
Thermal analysis results revealed an exothermic reaction at 640 °C, leading to the formation of the intermetallic compound Al3Fe.
      
The thermal analysis results matched well with the microstructures of the thermally simulated samples.
      
Thermal analysis results show that the complex is stable up to 100°C when it began to slowly decompose and followed by an explosive decomposition at 290°C.
      
The thermal analysis results of all these cyclohexanone inclusion compounds are reported.
      
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This paper describes the simultaneous thermal analysis of UO_2 from ADUprocess and discusses the relation between the thermal analysis results andthe forming and sintering characteristics,specific surface,higher oxides,alsogives the criterion of sinterability.It is important to guarantee the quality ofUO_2 powder and pellet fabrication.

本文介绍了由 ADU 分解还原得来的 UO_2粉末氧化过程的差热(DTA)、热重(TG)同时分析,讨论了热分析结果与成型烧结性、比表面、高价铀化物存在的关系,得出了检验 UO_2粉末的烧结性、高价铀化物存在等判据,为保证 UO_2 粉末及其芯块研制的质量起了重要作用。

In this paper, the physico-chemical properties, infrared spectrum and differential thermal analysis results of anti-settling aluminate(ASA) have been reported(?) After CaCO_3 was modified by ASA. the filling properties of CaCO_2, the change of the viscosity of CaCO_3/liquid paraffin System have teen studied. It has also researched the effect of ASA dosage, different dispersion medium and temperature on the settling properties of CaCO_3. In addition, the influence of ASA dosage for the settling velocity...

In this paper, the physico-chemical properties, infrared spectrum and differential thermal analysis results of anti-settling aluminate(ASA) have been reported(?) After CaCO_3 was modified by ASA. the filling properties of CaCO_2, the change of the viscosity of CaCO_3/liquid paraffin System have teen studied. It has also researched the effect of ASA dosage, different dispersion medium and temperature on the settling properties of CaCO_3. In addition, the influence of ASA dosage for the settling velocity and relative settling height of CaCO_3 in equilibrium have been compared with TEXAPHOR—963 made in Germany and CF—88 made in China. The experimental results show that CaCO_3 has made good functions in reducing viscosity and anti-settling after modified by ASA. The effects are obviously superior to TEXAPHOR—963 made in Germany and CP—88 made in China.

本文报导了防沉降性铝酸酯(Anti-Settling Alumjnate简称AsA)的理化性质、红外光谱和差热分析的结果。研究了用AsA改性碳酸钙后,碳酸钙填充性、碳酸钙/液体石蜡体系粘度的变化,以及ASA用量、不同分散介质对碳酸钙沉降性的影响。比较了ASA、西德的TEXAPHOR—963和国产的CP—88防沉降剂性能及其用量对碳酸钙的沉降速率、平衡后相对沉降高度的影响。研究结果表明,ASA改性碳酸钙后有很好的降粘和防沉降作用,效果明显优于西德的TEXAPHOR—963和国产的CP—88型防沉降剂。

The dynamic mechanical properties and thermal behavior of gamma radiation crosslinked LDPE/EPDM blends have been investigated over a temperature range from -50 to 100℃ and-70 to 150℃respectively. The results show that there is a damped peak (tanδmax) of about -20℃ in the dynamic mechanical spectra, and the peak temperature is denoted as Tβg, but the damped peak in low temperature region for each of LDPE and EPDM in blends disappeared. After irradiation, the Tβg of the LDPE/EPDM blends still appeared on the spectra,...

The dynamic mechanical properties and thermal behavior of gamma radiation crosslinked LDPE/EPDM blends have been investigated over a temperature range from -50 to 100℃ and-70 to 150℃respectively. The results show that there is a damped peak (tanδmax) of about -20℃ in the dynamic mechanical spectra, and the peak temperature is denoted as Tβg, but the damped peak in low temperature region for each of LDPE and EPDM in blends disappeared. After irradiation, the Tβg of the LDPE/EPDM blends still appeared on the spectra, and gamma radiation does not affected the compatibility of LDPE and EPDM. The thermal analysis results reveal that the fusion temperature Tm of irradiated LDPE/EPDM systems decreases with the increase of radiation doses.

本文报道了~(60)Coγ辐照LDPE/EPDM共混物的动态力学性能和热行为。在动态力学性能谱上出现两个转变,-20℃左右的转变是LDPE的β转变和EPDM玻璃化转变相叠加的转变,其峰温简称T_(βg),转变峰较平坦,表明LDPE/EPDM具有一定相容性;在69℃附近的另一个转变是LDPE的结晶预熔温度,随辐照剂量的增加而下降。未辐照的α转变活化能为106kJ/mol,辐照后活化能下降至80kJ/mol左右。用DSC法在所利用的剂量范围内,EPDM的T_g随剂量变化甚微,共混物的T_(βg)则不明显。LDPE的T_m辐照后有所下降,结晶度略有改变。

 
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