查询词典 acid group

B. Each kind of nucleic acid is composed of three parts: Molecular azotic basic group + member pentose + molecular phosphoric acid radical, DNA is by C, H, O, N, the P five kind of elemental compositions. c. The nucleic acid azotic basic group may divide into four kinds: Guanine, thymine, adenine, cytosine d.

b。 每一种核酸由三个部分所组成：一分子含氮碱基+一分子五碳糖+一分子磷酸根，DNA都是由C、H、O、N、P五种元素组成的。

The structural and photocatalytic properties of TiO〓 as well as surface acidity were greatly improved by sulfation. SO〓〓/TiO〓 solid superacid with Hammett constant Ho less than -12.14 was prepared by treating the TiO〓 with 1.0mol. L〓 sulfuric acid solution and then calcining at 450℃ for 3h. When compared to unmodified TiO〓, the SO〓〓/TiO〓 superacid catalyst exhibited higher anatase content, smaller crystal size, higher specific surface area, centralized pore size distribution, and the blue-shifted band edge of uv-vis adsorption spectra. Furthermore, the SO〓〓/TiO〓 superacid also showed excellent reaction activity and stability for CH〓Br photocatalytic decomposition even under the moist reaction conditions. The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明：SO〓〓与TiO〓表面的结合为螯合式双配位结构；TiO〓光催化剂表面经H〓SO〓浸渍处理后，提高了表面酸性，改善了催化剂结构和光催化性能，当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时，可制得SO〓〓/TiO〓超强酸催化剂(H〓＜-12.14)，其结构和光催化活性得到明显改善，与TiO〓相比，SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移，具有优异的光催化氧化活性、稳定性及抗湿性能，光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级，是一种有实际应用前景的高效光催化剂；由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型，认为在SO〓〓/TiO〓超强酸催化剂表面，由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心，其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移，具有可逆吸附水的性能，是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明：SO〓〓与TiO〓表面的结合为螯合式双配位结构；TiO〓光催化剂表面经H〓SO〓浸渍处理后，提高了表面酸性，改善了催化剂结构和光催化性能，当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时，可制得SO〓〓/TiO〓超强酸催化剂(H〓＜-12.14)，其结构和光催化活性得到明显改善，与TiO〓相比，SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移，具有优异的光催化氧化活性、稳定性及抗湿性能，光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级，是一种有实际应用前景的高效光催化剂；由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型，认为在SO〓〓/TiO〓超强酸催化剂表面，由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心，其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移，具有可逆吸附水的性能，是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

A-Methylnaphthalene contains a methyl group, which is a strong donor group, so the reaction of a-methylnaphthalene with C14 AOS acid had a higher conversion of aromatic than did the reaction of benzene with C14 AOS acid. After alkylaryl sulfonic acid is formed, it will continue to react with another AOS acid to rapidly produce dialkylaryl disulfonic acids owing to the electron- donating effect of the long alkyl chain in the alkylaryl sulfonic acid molecule.

a-Methylnaphthalene包含一个甲基集团，这是一个强大的捐赠团体，所以 a-methylnaphthalene反应出了与C14酸更高的转换的反应比苯与C14活性氧酸。alkylaryl磺酸为后形成，它将继续与另一出酸 dialkylaryl disulfonic迅速产生的电子-酸捐赠的长期效果在alkylaryl烃链磺酸分子。

Polyaspartic acid is easily ring-opened to form polyaspartic acid derivatives with a side chain founctional group.The second component can be added into aspartic acid by copolymerization to improve polarity and crystallization of primary polymer,and can make primary polymer without reactive group functionalize.

聚天冬氨酸是近几年来在全球销量日增的绿色化学品，由于它具有类似蛋白质的酰胺键结构，是一种生物可降解材料[1-2]，最终可降解成水和二氧化碳，具有良好的生物相容性，对环境友好。

Part 2:(1). Twenty-four rats were divided into 4 groups and wereadministrated uric acid, oxonic acid, oxonic acid + uric acid (OA+UA group) and oxonic acid + pyrazinamide (OA+PZA group) i.p.

天津医科大学博士研究生学位论文第四部分：将30只大鼠随机分为五组，在腹腔注射氧嚓酸+毗嚓酞胺建立HU模型的基础上，分别用中汇痛风定、中药l、中药2和中药3每日灌胃1次。7天后比较尿酸代谢的变化。

Sheep tibetan antelope by wool horn albumen the composition of amino acid and goat, sheep by wool fibre identical; but there is certain difference on the content scale of all sorts of amino acid, acid content of ammonia of group of cashmere tibetan antelope is 5.88%, all the acid content of ammonia of content; guang of acid of ammonia of the group in prep above cashmere wool and continous abb is 10.60%, alkalescent and amino acid and acidit

藏羚羊被毛角蛋白氨基酸的组成和山羊、绵羊被毛纤维相同；但在各种氨基酸的含量比例上有一定的差异，藏羚羊绒组氨酸含量为5.88%，均高于山羊绒和绵羊毛中组氨酸的含量；胱氨酸含量为10.60%，高于其它所测山羊的绒和毛；碱性氨基酸和酸性氨基酸含量接近(14.87%，15.23%)；藏羚羊绒促螺旋蛋白含量低于降螺旋蛋白。

Methods: Randomly subgrouping the rat into normal group, model group, paishi granule up, and Yiqi Huoxue Paishi decoction group, except the normal and model group, rats in other groups were all intragastrically administrated with 1.25% Ethylene Alcohol plus 1% ammonia chloride, then to observe the Ca(superscript 2+), Mg(superscript 2+), P(superscript 3+), uric acid of the blood serum and urine, the ethanedioic acid in renal tissue.

随机将大鼠分为正常组、模型组、排石冲剂对照组和益气活血排石饮组，除正常对照组外，以1.25%乙二醇合1%氯化铵灌胃制作大鼠草酸钙肾结石模型，观察各组大鼠血清Ca(上标 2+)、Mg(上标 2+)、P(上标 3+)、尿酸及肾组织草酸以及尿Ca(上标 2+)、Mg(上标 2+)、P(上标 3+)、与尿尿酸的含量。

Methods: To divide 102 patients with elderly hypertensive into 3 groups according to the difference of blood pressure result, and compare the relationship between serum uric acid and blood pressure among the different groups. They were divided into normal group、intimae tricking group、plaque shaping group and vascular stenosis group accoraing to ultrasound result. To compare the serum uric acid level and blood pressure among each group.

将102例老年高血压患者按血压值的不同分为三组，比较各组间血尿酸与血压的相关性，对各例患者分别检测血生化指标：空腹血糖、血尿酸、甘油三脂和总胆固醇，B超观察颈动脉变化，按B超结果将患者分为内膜正常组、内膜增厚组、斑块形成组和管腔狭窄组，比较各组间血压、血尿酸水平。

The result indicated that MgO and α- methacrylic acid can together thicken epoxy, and the speed of thickening epoxy become quickly with the increasing content of MgO; when the ratio of MgO and α- methacrylic acid is 3:1, thickening epoxy have a better effect; the thickening mechanism: the terminal corboxyl group of α- methacrylic acid react with MgO, and it accompany with large numbers of heat, the heat can accelerate the reaction between the terminal corboxyl group with the secondary hydroxyl groups of epoxy, intermolecular hydrogen bonding which the water of above-mentioned formation result in and complex compound which format the metal atoms and carbonyl group complexing collective increase the viscosity of epoxy resin.

结果表明：MgO和α－甲基丙烯酸配合可增稠环氧树脂，随着MgO加入量的增加，环氧树脂增稠的速度加快；MgO与α－甲基丙烯酸为3：1时，增稠环氧树脂的效果较好；推测环氧树脂的增稠机理是α－甲基丙烯酸中的端羧基与氧化镁反应，放出热量促使其端羧基与环氧树脂中的仲羟基反应，上述反应生成水产生的氢键和羰基与氧化镁中的金属原子形成络合物共同导致环氧树脂的粘度增加。

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