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Among these samples, two samples with 5wt% and 15wt% carbon obtained from the grape sugar have an excellent electrochemical performance. The first discharging capacity of the sample with carbon content of 5% is 132.5 mAh/g and the other is 145.4mAh/g.

其中掺杂葡萄糖后灼烧而成、含碳量5%和15%的样品的初始放电比容量分别为132.5 mAh/g和145.4 mAh/g。

It was found that the initial capacity of amorphous manganese dioxide was 208 mAh.

无定型二氧化锰首次放电容量为208 mAh.g-1，第五次循环的放电容量为首次的80.6%，即167.6 mAh.g-1。

This result was consistent with the previous simulation study;(2) the signals of MAH onto the radical chain ends with double bonds increased markedly with increasing MAH content, indicating that P scission occurred after MAH attached to the tertiary carbons.

MAH的用量对接枝PP链的等规度有很大的影响，主要表现在随MAH浓度增加，PP链的mm序列所占的比例逐渐增大，mr和rr序列所占的比例逐渐减小。

The results show that the alloys are composed of LaNi5 as matrix and LaNi3 as secondary phase. With the increasing Sm substitution for La, the unit cell volume of matrix of the alloys shrinks linearly and both the hydrogen storage capacity and discharge capacity decrease. When the Sm substitution is 0.1, 0.2 and 0.3, the discharge capacity decreases from 380 mAh/g to 370(362), 355(334) and 329(295) mAh/g, respectively. However, the rate performance and cycle stability is improved. After 100 cycles, the capacity loss decreases from 20% to 18%(17%), 16%(14%) and 13%(11%).

结果表明：该合金是由LaNi5主相和LaNi3第二相构成；随著Sm取代La量的增加，合金主相单胞体积线性收缩，合金储氢量和放电容量减小，当Sm取代量分别为0.1、0.2、0.3时，合金容量由380 mAh/g分别减小到370(362)、355(334)、329(295) mAh/g，但高倍率放电能力和循环稳定性得到改善，100次循环后的容量损失率由20%分别降低到18%(17%)、16%(14%)、13%(11%)。

A study of phase morphology of PBT/POE-g-MAH/nano-CaCO3 composite by means of scanning electron microscopy showed that the domains size of nano-CaCO3 capsulated by POE-g-MAH elastomer in composite when PBT was mixed directly with POE-g-MAH and nano-CaCO3 together or with nano-CaCO3 capsulated by POE-g-MAH elastomer is large.

采用熔体流动速率较低的EPS30R与纯POE-g-MAH共混制备的增韧改性剂，在PBT基体中的分散相变得粗大且不均匀，共混物的脆韧转变推迟。SEM显示，纯POE-g-MAH增韧剂使PBT共混物发生脆韧转变时，弹性体分散相颗粒产生塑性变形，诱发基体屈服而吸收能量。

When the concentration of MAH is higher than that of St, some MAH monomer reacts with St to form SMA, others can directly grafts onto PP macroradicals. When the amount of St added is higher than that of MAH, part of St monomer may preferentially react with PP macroradicals to form more stable styryl macroradicals, while others copolymerize with MAH, yielding SMA. MFR of the grafted PP is lower in this case. It is considered that MFR of the grafted PP is decided by concentration of free monomers, or, number of grafting reactive species. FTIR analysis confirmed the above mechanism.

当MAH单体用量多于St单体时，一部分MAH单体与St反应生成SMA，另一部分可直接与PP大分子自由基进行接枝反应；当St单体用量多于MAH单体时，除与MAH反应生成SMA之外的St单体可先与PP大分子自由基反应，并起到稳定PP自由基的作用，这时接枝物的MFR较小，亦即接枝物的MFR与体系中可进行接枝反应的活性种数目有关。

The flame retardant PP-g-MAH/OMMT nanocomposite master batch was prepared with maleic anhydride grafted polypropylene and organophilic montmorillonite by melt intercalation. The master batch was characterized by means of XRD and TGA. Flame retardant PP with high flame retardancy and mechanical properties was prepared with PP-g-MAH/OMMT master batch and magnesium sulfate whisker.

以聚丙烯接枝马来酸酐和有机蒙脱土为原料，通过熔融插层制备了PP-g-MAH/OMMT纳米复合阻燃母料，利用X射线衍射及热失重分析对其进行了表征，并将其与碱式硫酸镁晶须复配，制备了阻燃性能及力学性能优良的阻燃PP。

A new view of reaction mechanism of polyethylene grafted maleic anhydride was put forward based on experiment results.(4) EDA has obvious inhibition ability to the cross-linking by-reaction of PE grafted MAH ,which can show MI increase and stabilization with the EDA increasing.

在PP接枝MAH的研究中发现：（1）PP/DCP反应挤出体系呈现典型的降解过程，表现为MI随DCP增加而显著上升，EDA对该体系的降解无抑制作用；（2）在PP/DCP/MAH反应挤出接枝体系中，随DCP增加，MI上升而Gx下降；随MAH增加，MI下降而Gx呈上升趋势。

The blends of PE-g-MAH and gelatin were prepared by melting process and the compatibility of PE-g-MAH and gelatin in blends were characterized. The results of FTIR showed that the characteristic absorption band peaks of amine and amide groups of gelatin were shifted in PE-g-MAH/Gelatin blends, the equilibrium values of torque were higher with the increase of blending temperature, which proved that graft copolymer PE-g-MAH-g-gelatin was formed during the preparation process, and the amount of PE-g-MAH-g-gelatin was increased with increasing the amount of PE-g-MAH. SEM micrographs exhibited that there was PE-g-MAH-g-gelatin formed in surface of gelatin phase.

通过红外光谱分析、HAAKE流变分析、抽提等实验证明：共混物中明胶的氨基、酰胺基团吸收峰峰位发生了明显的变化；在熔融共混过程中，随着温度的提高，平衡扭矩增大；明胶与PE-g-MAH发生了反应形成PE-g-MAH-g-明胶接枝共聚物，而且随着PE-g-MAH用量的增加，形成接枝共聚物的量也提高；SEM的实验结果表明，在明胶的表面确有接枝物形成；通过DMA测试共混物的玻璃化转变温度，发现两组分的玻璃化转变温度差值减小，二者的相容性提高，实现了共混体系的自增容。

It was shown that the absorption peaks of amine and amide groups of gelatin were shifted in HDPE/PE-g-MAH/Gelatin blends because of the reaction of PE-g-MAH with gelatin. The addition of PE-g-MAH made the increase of HDPE glass transition temperature. The compatibilizing effect of PE-g-MAH was due to the crystal compatibility produced by forming the co-crystals of HDPE, PE-g-MAH and PE-g-MAH-g-gelatin. The blends of EAA and gelatin were prepared by melting process and the compatibility of the blends was also studied. The FTIR results showed that absorption peaks of amine and amide groups of gelatin were shifted in EAA/Gelatin blends.

通过红外光谱分析、HAAKE流变分析、抽提等实验证明：共混物中明胶的氨基、酰胺基团吸收峰峰位发生了明显的变化；在熔融共混过程中，随着温度的提高，平衡扭矩增大；明胶与PE-g-MAH发生了反应形成PE-g-MAH-g-明胶接枝共聚物，而且随着PE-g-MAH用量的增加，形成接枝共聚物的量也提高；SEM的实验结果表明，在明胶的表面确有接枝物形成；通过DMA测试共混物的玻璃化转变温度，发现两组分的玻璃化转变温度差值减小，二者的相容性提高，实现了共混体系的自增容。

For a big chunk of credit-card losses; the number of filings (and thus charge-off rates) would be rising again, whether

年美国个人破产法的一个改动使得破产登记急速下降，而后引起了信用卡大规模的亏损。

Eph. 4:23 And that you be renewed in the spirit of your mind

弗四23 而在你们心思的灵里得以更新