分解温度

发泡剂AC的用量、分解温度对孔隙结构具有明显的影响。

The amount of the vesicant AC and the decomposition temperature present evident influence on the pore structure .

混合溶液中制备的Ag2O纳米粒子的分解温度比正常状况下低得多。

The decomposition temperature of as prepared Ag_2O was much lower than that of macroscopical one .

选择季戊四醇降低了发泡剂H的分解温度；

Choice The decomposing temperature of foamer H was dropped by using pentaerythrite .

适宜的热分解温度有利于含Ce涂层阳极性能的提高，最佳温度为450℃。

The optimal temperature of thermal decomposition is at about 450 ℃ .

发泡助剂如氧化锌和硬脂酸锌的加入能有效地降低偶氮二甲酰胺（简称AC）的分解温度，改善发泡效果。

The decomposing temperature of azodicarbonamide ( AC ) could be decreased and the frothing effect was improved by blowing promoter .

ABS纳米管的分解温度比本体ABS低100℃左右。

The ABS nanotubes have a lower thermal decomposition temperature 100 ℃ lower than its bulk polymer .

用DSC差示扫描量热仪测定了各体系的动态分解温度和热效应。

The dynamically decomposing temperatures and the heat effects of different systems were determined by DSC .

采用DSC、TGA/DTG对其热性能进行了研究，发现随着TDI的加入，共聚物的熔点升高、熔融热增加，即材料的结晶度增大，同时材料的热分解温度亦随之升高。

With the addition of TDI , the melting temperature and the enthalpy increased .

DSC研究结果表明再生柞蚕丝素纤维的热分解温度和天然柞蚕丝素纤维的热分解温度相似；

The results of DSC showed that decomposition temperature of regenerated fibers was similar to native fibers .

产物的颜色、分解温度、IR及~1HNMR亦与取代基有一定关系。

And the colour , decomposition temperature , IR and 1H NMR of the products have a certain relation to their substituent .

当质量损失为5%时复合材料的热分解温度较纯CE提高23.8℃；

And when the mass loss of composites was 5 % , its degradation temperature improved 23.8 ℃ compared with pure CE .

TiO2／BMI固化树脂玻璃化温度高达302℃，热分解温度达420℃；

The glass temperature of TiO 2 / BMI cured resin was 302 ℃, thermal decomposition temperature was 420 ℃ .

选用季戊四醇及尿素降低了发泡剂H的分解温度，解决了泡体的交联速率与发泡剂的分解速率相配合的问题；

Solving the cooperation problem of crosslinking velocity of foam and decomposing velocity of blowing agent through reducing the decomposing temperature of blowing agent H by adding pentaerythrite and carbamide ;

TGA测试则说明了该树脂具有较好热稳定性，起始分解温度大于300℃。

The resinous compound has a good heat-resistance , and thermal-degradation begins at temperature higher than 300 ℃ .

TGA对前驱体的热分析表明微波处理能降低分解温度。

The thermogravimetric analysis ( TGA ) of the MgO precursor indicates that microwave can reduce the decomposition temperature .

PP/OvPOSS复合材料的热分解温度低于纯PP，但反应共混复合材料和OvPOSS-g-PP的热稳定性高于物理共混复合材料。

PP / OvPOSS composites have lower degradation temperature than PP , and the reactive blending composites have better thermal stability than that of the physical blending ones .

采用热重分析TG和DSC分析了大豆蛋白纤维的热学特征，得出大豆纤维的玻璃化温度和分解温度。

The thermal property of the soybean protein fibers was analyzed by TG and DSC . The glass transition temperature and decomposition temperature are obtained .

采用DSC和TG技术分别分析了一水盐酸环丙沙星晶体的脱水、熔化、分解温度和晶体的水含量；

The deaquation , melting , decomposing apex temperatures and water content of ciprofloxacin hydrochloride monohydrate crystals were measured by DSC and TG techniques respectively .

与纯PMMA相比，PMMA/TiO2杂化材料的热分解温度由270℃升高至300℃左右。

Comparing with pure PMMA , the thermal decomposition temperature of PMMA / TiO2 hybrid materials rises from 270 to about 300 ℃ .

TGA结果表明共混树脂固化物具有很好的热稳定性，其起始热分解温度接近400℃。

The results of TGA indicate that the blends possess high thermal stability with initiation decomposition temperatures of about 400 ℃ .

PAN-PPO的热分解温度略低于聚苯胺（PAN）；

The degradation temperature of PAN-PPO was a little lower than that of PAN .

利用变温IR光谱、变温X&射线粉末衍射图和酸碱滴定曲线，对配合物的分解温度以及在水溶液中稳定存在的pH值范围进行了初步探讨。

We use variable-thermal IR spectrum , variable-thermal powder X-ray diffractogram and acid-base titration curve to approach the decomposition temperature of the coordination compounds and their pH range of stability in water solution .

随共聚物中液晶性单体含量增加，共聚物玻璃化转变温度Tg和热分解温度Td有所上升，但Tg的变化较小。

The glass transition temperature and decomposition temperature of the copolymers changed with the increase of the contents of mesogenic monomer units in the copolymers .

结果发现：不同浓度的醋酸对ABS粒子分解温度的影响不同，且ABS粒子和ABS染色柱子的耐药性也不同。

The experimental results show that the chemical resistance of ABS pellet was different from ABS dyeing pellet when they were soaked in acetic acid with different concentrations .

借助变温IR、变温XRD和TGDTA研究了它们的热稳定性，表明配合物的热分解温度是450～500℃；

Their thermal stability studied by TG DTA , IR and XRD at various temperatures show that the range of temperature of pyrolysis is 450 ~ 500 ℃ .

TG和WAXD实验结果表明，采用共插层剂改性的蒙脱土的片层间距显著增大，且热分解温度较高；

TG and WAXD results show that MMT modified by co-intercalating agents has more larger interlamellar spacing and higher thermal decomposition temperature .

OME含量对ADN的起始热分解温度有明显的影响。

Furthermore the initial decomposition temperature of ADN is subject to the content of OME evidently .

选用EPDM作橡胶介质，重点测试了发泡剂H在EPDM胶料中的分解温度、发气量及分解速度等参数。

The decomposition temperature ( Td ), gas evolution and decomposition rate of blowing agents , especial blowing agent H ( dinitrosopentamethylenetetramine ) in EPDM compounds were investigated .

用TGA对其耐热性能进行了评价，4-APM树脂固化物的起始分解温度为414℃，在900℃的残重为51%；

The TGA characterization indicated its onset decomposition temperature was 414 oC , and the residue mass was 51 % at 900 oC .

通过DSC、TG、及溶解性能测试结果表明，该聚合物表现出较高的玻璃化转变温度、良好的热稳定性（高的热分解温度）及溶解性能。

The products were characterized by DSC and TG . The results showed that these polymers were of higher glass transition temperatures , better thermal stability and good solubility .