degradation of energy

degradation of energy的基本解释

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能的退降

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能的递降

与degradation of energy相关的网络例句 [注：此内容来源于网络，仅供参考]

The results showed that (1) The grain size of nanometer YiO_2 was40～80nm.The wavelength corresponding to the maximum absorbency values were observedin the 200～320nm range.The crystal structure of carbon doped TiO_2 photocatalyst is primarilyanatase(22.43% rutile), and the content of carbon is about 4.6%.(2) The relative humidityvaring from 8% to 80%, the photocatalytic degradation degree of benzene increased withincreasing relative humidity; and to toluene, degradation rate was hanced by relative humidityup to 60%, and more or less inhibited above 60%.(3) Scheme and results of orthogonal testswere used by evaluating the photocatalytic performance of the gas phase methanol, acetoneand 1-heptane.The results revealed that their degradation degree reached 84.5%, 93.39% and93.45%, respectively.(4) The 254nm UV lamp showed higher photocatalytic degradation rate.For methanol, acetone and 1-heptane, it was found that photocatalytic degradation reactionoccurs with the light strength of daylight lamp.(5) Under the the same conditions, 15%degradation degree has been obtained for benzene, whilst about 10% degradation degree wasattained by Degussa P25; During the initial phases, the toluene revealed higher photocatalyticactivity, comparing with Degussa P25, the degradation degree of methanol, acetone and1-heptane were slightly lower.

结果表明：(1)CVD法制备的纳米TiO_2光催化剂，颗粒球形度好、粒径在40～80nm之间；最大吸光度值所对应的波长为200～320nm；含碳量约为4.6％；晶型组成主要为锐钛矿型，金红石的含量约为22.43％；(2)在相对湿度为8％～80％范围内，苯的光催化降解率随着相对湿度的增大而增大；甲苯在相对湿度为60％时达到最好降解效果，当相对湿度增大到80％时光催化效果降低；(3)将正交实验设计及实验方案应用于气相甲醇、丙酮和正庚烷光催化降解研究，实验结果表明：三者最高降解率分别为84.5％、93.39％和93.45％；(4)有254nm紫外灯参与的光催化实验可以大大提高有机气体的光催化降解率；在日光灯的照射下，掺碳纳米TiO_2对气相甲醇、丙酮和正庚烷具有一定的光催化氧化能力；(5)较P25粉，在相同的光催化操作条件下：气相苯的平均降解率达15％，高于P25粉10％的降解率；气相甲苯在初始阶段具有较高的反应速率；气相甲醇、丙酮和正庚烷的降解率略低于P25粉。

So, the average density of spatial energy of spatial radius is the length of Planck of relative time-space cosmic energy follow the rise and fall of quantum spatial measurement, at original cosmic time-space set out, from the structure-energy of mass 16.38×10-71 N · m to the space-energy of 8.19×10-71 N · m and the mass-energy of 8.19×10-71 N · m, come to do not exceed the structure-energy of mass 32.76×10-71 N · m to the space-energy of 8.19×10-71 N · m and the mass-energy of 24.57×10-71 N · m, not smaller the structure-energy of mass 21.84×10-71 N · m to the space-energy of 8.19×10-71 N · m and the mass-energy of 13.65×10-71 N · m, come to do not symmetrically gradually belong to stabilization thus at reductively fluctuate, not can reversely strides across reach the stable state of structure-energy mass 24.57×10-71 N · m to the space-energy of 8.19×10-71 N · m and the mass-energy of 16.38×10-71 N · m maintain unchanging.

所以，宇宙能量的相对时空空间的半径为普朗克长度的空间的能量平均密度随宇称量子的涨与落，在原初的宇宙时空启动，从16.38×10-71N · m 质量结构能对于8.19×10-71N · m 空间能与8.19×10-71N · m 质能，成不大于32.76×10-71N · m 质量结构能对于8.19×10-71N · m 空间能与24.57×10-71N · m 质能，不小于21.84×10-71N · m 质量结构能对于8.19×10-71N · m 空间能与13.65×10-71N · m 质能，成不对称地递归于稳定而在缩小地波动，不可逆地跨越到24.57×10-71N · m 质量结构能对于8.19×10-71N · m 空间能与16.38×10-71N · m 质能的稳定状态保持不变。

Degradation test in vitro was carried out in phosphate buffer solution (0.1M, pH7. 4) at 37 ℃. The buffer solution was changed daily. Degradation test in vivo was implanted the sample to subdermal in adult ICH rat in the scapular area lateral to the dorsal midline. At suitable time the samples were recovered. Molecular weight changes in surface layer and bulk of polymer sample were measured by GPC and weight loss was determined gravimetrically. It was found that the degradation behavior can be regulated by changing the composition of copolymers. The critical compositions from surface to bulk degradation behavior for PGCA, PLCA, PLMCA, PLDCA systems were 15-20, 20-30, 30- 40, 40 of mol percent GA or LA unit in copolymers, respectively. The degradation behavior of PGCA, PLCA, PLMCA, PLDCA systems were compared and analysed. Some factors influencing the degradation character, such as copolymer composition, hydrophobicity, crystallinity and enzyme affect etc. played important role.

体外实验中材料降解环境为37℃，0.1M，pH7.4磷酸缓冲溶液，每天换液，定期取样；体内实验中将聚合物试样埋置于ICH小白鼠背部肩胛骨皮下部位，定期处死小鼠，取样，将体内体外样品进行重量损失及试样内外层分子量变化测定，分析各聚合物试样降解行为特性，实验结果证明，改变共聚物组成，可以调节各聚合体系降解行为特性，对PGCA，PLCA，PLMCA，PLDCA共聚体系，交酯摩尔百分含量15-20％，20-30％，30-40％，40％分别为各体系内降解行为特性由表面降解型向本体降解型过渡的临界转折点，交酯含量较低的聚合物不同程度地表现表面降解行为特性，论文对各共聚体系体内外降解行为作了分析对照，例如共聚物组成对材料降解速度与降解行为的影响；生物体内酶对降解行为的影响；材料亲疏水性，聚合物链段结晶行为及碳酸酯结构对材料降解行为的影响等，得出交酯/环碳酸酯共聚体系降解行为一些共性和规律。

与degradation of energy相关的网络解释 [注：此内容来源于网络，仅供参考]

degradation of energy：能量退降,能量递降

deformation 形变 | degradation of energy 能量退降,能量递降 | degree 度

degradation of energy：能量衰减

degeneration 退化 | degradation of energy 能量衰减 | degree fahrenheit 华氏温度

degradation of energy：能的退降

degeneration 简并化 | degradation of energy 能的退降 | degraded color 递减色

degradation of energy：能量散逸

degradation 软化 | degradation of energy 能量散逸 | degraded spectrum 软化谱

law of degradation of energy：能量退降律

law of definite proportion 定比定律 | law of degradation of energy 能量退降律 | law of demand 需求定律,需求律