水合的

The established models in which annual precipitation was incorporated as the principal variable indicate a very closely correlation between forest productivity and its corresponding climatic factors,allowing to simulate distribution pattern of actual forest productivity effectiv...

结果表明：在所构建的模型中，除海拔高度与净生产力的相关模型外，其它模型均有较高的实用价值，模型的拟合曲线变化，基本反映了中国森林现实生产力的地理分布格局；中国森林生产力的分布格局主要取决于气候环境中的水热条件，水分条件是决定中国大部分地区森林生产力水平和地理分布格局的主导因素；根据7个GCMs大气环流模型预测合成的2030年的气候情景，研究气候变化对中国森林生产力影响的结果是：气候变化并没有改变中国森林第一性生产力的地理分布格局，即从东南向西北森林生产力递减趋势不变，但不同地域的森林生产力有不同程度的增加。

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。

Following, a experiment has been carried out, the incident waves with a frequency band of 200kHz-3 50kHz are used to the experiment, and a series of peak value-time curves are drawn each 10kHz, corresponding time are found through fitting peak value, thus the position of the defect is calculated accurately. The application of awl-shaped sensor head in the heat change water pipe experiment indicates that the ultrasonic guided waves may transmit nearly 50 meters in the pipe, which is not influenced by the elbows and makes it possible to test defects in long distance and large-scale. The water-load pipe experiment indicates that the displace and energy maybe leakage at the near-surface, which is significant for the further research.

而后，采用200kHz至350kHz频段的入射波进行了实验验证，并每隔10kHz绘出一条峰值一时间的曲线，通过拟合峰值点，找到对应的时间，从而准确的计算出了缺陷的所在；应用锥形探头的热交换水管的实验表明，超声导波可以在管道中传播了近50米的距离，且不受弯头的影响，从而使得长范围、大规模检测成为可能，水载管实验说明了离面位移和能量可能会发生泄漏的特性，为导波的深入研究和应用作了铺垫。

In the present dissertation, a surfactant-templated mesoporous silica molecular sieve with high pore volume, high porosity and narrow bimodal mesopore size distribution was synthesized for the first time in a reaction system, which was used usually in the synthesis of mesoporous MCM-41 molecular sieves, by a judiciously controlled two-phase sol-gel processing under basic conditions.

在本论文中，我们通过对一个通常用于制备介孔MCM-41分子筛的反应体系中正硅酸乙酯水解与缩合反应相对速率的精确调控，首次在弱碱性体系中合成了一种具有高孔隙率、大孔体积和双介孔孔分布特征的新型二氧化硅分子筛材料，简记为BMS，并对BMS二氧化硅分子筛中双介孔结构形成的原因及各种可能对其结构和性质产生影响的合成因素如Ammonia／silica摩尔比、组分浓度的变化、表面活性剂烷基链长度的调节、辅助有机物均三甲苯的引入、催化剂的结构和性质、溶剂和助溶剂的极性和用量、老化和干燥条件的变化及合成后水热处理等，利用不同的测试手段如XRD，SEM，TEM，〓Si MAS NMR，TG-DTA，N〓吸附测试等进行了系统的表征研究。

Single component and multi\|component of iron system colloidal catalyst \Ali\|Bu\-3CH\-2CHCH\-2Cl\ were mixed by different ratios in hydrogenated gasoline medium at 25℃.This paper studied the relationship between the nonaqueous systematic electroconductivity and the concentration of catalyst components.In combination with Tyndall effect,polymerization experimental results,Ali\|Bu\-3 existed in associated state and dissociated into ionpair.The reaction between Ali\|Bu\-3 and Fenaph\-2 was the main reaction which formed colloidal core.Ali\|Bu\-3 reacted on CH\-2CHCH\-2Cl and Ali\|Bu\-2Cl was yielded which joined the formation of active center on the surface of colloidal core.The excessive Ali\|Bu\-3 was dissociated into ionpair which formed double electrode layer,and the double electrode layer kept the colloidal particles relatively stable.

研究了在25℃加氢汽油介质中，铁系胶体催化剂［Fenaph2Ali-Bu3―CH2==CHCH2Cl］单组分、多组分按不同配比混合，非水体系电导率与浓度的关系，结合Tyndall效应，聚合实验结果，得出Ali-Bu3以缔合状态存在并解离成离子对它同环烷酸亚铁的作用是形成胶核的主要反应，与氯丙烯反应生成的氯化异丁基铝，在胶核表面参与形成活性中心由过量Ali-Bu3解离的离子对形成的双电层结构，使胶粒保持相对稳定。

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