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The pilot study shows that the ammonia dissociation/synthesis reaction is inherently free of any potential side reaction problems, and also offers phase separation of products. The carrier of heat store is liquid. and is very interesting for long-term storage as it can be carried out at room temperature with no energy losses, Its theoretics energy storage density reachs 66.5kJ/mol, which outclasses sensible or latent heat storage. In comparison to other thermochemical energy storage, ATCES needs lower temperature in endothermic reaction(only 650℃), but It can produce over 550℃ high temperature stream in exothermic synthesiser. Furthermore, the heat store/recovery can change with adapt to the heat source/load automatically, and offers coninuous(24 h) production of heat, These advantages will see a rapid increase in the adoption of large-scale concentrating solar thermal power generation.

初步研究表明：采用氨基储能体系，储/释过程无副反应，且储能介质能自然发生相分离；储热载体为流体，并可在室温下长期无热损储存，理论储能密度达66.5kJ/mol，远高于显热或相变蓄热；与其它热化学储能相比，吸热反应温度低，仅需650℃，而放热反应可产生500℃以上的高温，能量的储/释流量可随热源/负荷自适应变化，且可全天供热，更适合作为聚光式大规模太阳能热力发电中的能量储存系统。

The kinetics process and temperature impact of natural groundwater denitrified by sulfur autotrophic was investigated. The results revealed that the denitrification rate of up-flow sulfur autotrophic denitrification filter followed a half-order kinetics model; and the reaction rate constant was mainly affected by the temperature. Based on the Arrhenius calculation, the activated energy was 80.38 kJ/mol.

研究实际地下水硫自养反硝化动力学过程，考察季节因素对动力学的影响，实验结果表明，地下水升流式硫自养滤柱反硝化动力学符合1/2级动力学模型，其反应速率常数受温度的影响很大，用阿仑尼乌斯方程计算硫自养反硝化活化能为80.38 kJ/mol。

The protein purified with Ni-NTA column was denatured by 8 mol/L urea and dialyzed for refolding.

Ni-NTA柱纯化后的特异性蛋白经8 mol/L脲素变性，梯度透析使蛋白质复性。

Methods: NG108-15 cells were cultured in vitro at 37℃in a humidified atmospherecontaining 5％CO_2. Aβ_(25～35) fragment was dissolved with deionized distilledwater and aged for 4 days at 37℃. The cells were exposured to 5μmol/LAβ_(25～35) for 24h to establish the cell model. Twelve rabbits were divided intotwo groups at random, and garaged with MWD or physiological saline controlrespectively for 7 days to collect two kinds of cerebrospinal fluid, theyare CSF from rabbits treated with MWD and CSF from rabbits treated withphysiological saline.

NG108-15细胞在37℃、体积分数为5％的CO_2培养箱中培养，Aβ_(25～35)溶解于双蒸水中，置于37℃培养箱中老化4d，使其寡聚，毒性增强，细胞被置于浓度为5μmol／L的Aβ_(25～35)中作用24h，建立起AD细胞模型。12只清洁级大耳白家兔购于华中科技大学同济医学院动物中心，将其随机分成两组，分别给与等量的加味温胆汤和生理盐水灌胃7d，末次给药后1h内用水合氯醛将给药组白兔麻醉，1.2ml／kg，无菌条件下用7号注射针头从枕骨大孔处垂直进针，抽取清亮含药脑脊液。

In the 0.1 mol/L NaCl solution, addition of 5% MFP for immerging 1d shows the best inhibition effect.

在0.1 mol？L-1 NaCl溶液中，添加5% MFP浸泡1d缓蚀效果最明显。

METHODS: Acetic acid solution was added into chitosan to prepare 8% chitosan acetic acid hydrosol, which was then stayed for one day. Flowing the immersion into the hydrosol and immediate dislodgement, plastic tube was soaked in 1 mol/L sodium hydroxide for 3 minutes. Hydrosol out of the tube etiolated and coagulated into jells, the tube was removed when the jells were semi-dried.

利用乙酸溶液制备8%壳聚糖乙酸水溶胶，溶胶放置1 d，将硬塑料管浸入溶胶后迅速取出放入1 mol/L氢氧化钠液内3 min，见管外溶胶变白凝固成胶冻状，取出后晾到五分干后轻轻退下内管，晾干后即成为壳聚糖导管。

According to the physiochemical properties of anthocyanin, methanol solution containing 0.1 mol/L HCl was selected as the extraction solution, then grape pomace lixiviated for 30～40 min with pH=3.0～4.0 and temperature at 60～70 ℃, and then the liquid or paste extract was prepared after a series of technical procedures including extraction, centrifugation, filtration and vacuum concentration.

本课题根据花色素苷的理化性质，选择了用0.1 mol/L 的HCl的甲醇溶液作提取剂，在pH值为3.0～4.0及60～70 ℃温度下浸提30～40 min，再经萃取、离心、过滤、减压浓缩，可得到液态或膏状提取物，并通过了分析检测；还对花色素苷在食品工业中的应用作了研究。

Our study includes four aspects. In the first aspect we study several important conditions of porcine oocytes maturation in vitro and oocytes cleavage after parthenogenetic activation and found mNCSU-23+15IU/mlPMSG+20IU/mlHCG+15% PFF+0.57mMcysteine is a good culture condition .When the Cocs are cultured in it ,the maturation rate and oocytes cleavage rate are higher than those of foreign covered. Our result are (86.7±3.35)% and (86.3±4.16)% and the highest report of foreign is(85.7±4.1)%.In the second aspect we study the effect of different chemical activations on development of porcine parthennogenetic embryo and found two best activation method. The first one is that putting the maturation MII oocytes in the 20μmol/L ionomycin for 30 minutes and then putting them in the NCSU-23 condition containing 5μg/mICB and 5mM/L6-DMAP for 3.5 hours, the oocytes cleavage rate and morulae/blastocysts development rate are (76.7±7.6)% and (37.1±6.4)%.The second one is that putting the maturation MII oocytes in the 200μM/L Thimerosal for 20 minutes and then putting them in the NCSU-23 condition containing 8mM DTT for 30 minutes

本研究分为4个部分，第一部分对影响猪卵母细胞体外成熟和孤雌激活后胚胎分裂的几个重要条件进行了比较研究，确立了一种较好的培养方法：与颗粒细胞共培养，找到了一种适合猪卵母细胞体外成熟的培养基：mNCSU-23+15IU/mlPMSG+20IU/mlHCG+15%PFF+0.57mM半胱氨酸，成熟率和分裂率分别为(86.7±3.35)%和(86.3±4.16)%，国外报道的最高成熟率为(85.7±4.1)%；第二部分对猪卵母细胞孤雌激活的化学方法进行了研究，确立了化学激活猪卵母细胞的两种最佳方法：1将成熟的去卵丘颗粒细胞的MII期卵母细胞用20μmol/Lionomycin作用30min，再将卵母细胞培养于含5μg/mlCB和5mM/L 6-DMAP(6-二甲基氨基嘌呤)的NCSU-23培养液中，卵裂率和桑囊胚发育率达到(76.7±7.6)%和(37.1±6.4)%2将成熟的去卵丘颗粒细胞的MII期卵母细胞在200μM/L的Thimerosal中处理20min，再与8mM的DTT共孵育30min，卵裂率和桑/囊胚形成率为(81.0±2.8)%和(39.6±2.7)%；第三部分对孤雌激活胚胎的培养条件进行了研究，确立了一种最佳的胚胎培养条件：在SOF简单培养基中添加颗粒细胞进行前3天的培养，然后转入添加胎牛血清的NCSU—23培养基并和输卵管上皮细胞进行后期的培养，其桑椹胚和囊胚的发育率为(59.5±3.2)%；第四部分研究了IGF-I

Oxidizing reaction activation energy of the passivated Al nanopowder is more than 500KJ/mol.

钝化处理纳米铝粉氧化反应的活化能大于500KJ/mol。

Production and decomposition of the peroxides were investigated. The active energy of peroxides decomposition equals to 27.2 kJ/mol.

研究了过氧化物的产生和分解，计算出过氧化物分解的活化能为27.2kJ/mol。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。