生孢噬纤维粘菌基因文库的构建和纤维素酶基因的克隆

将生孢噬纤维粘菌（ＳｐｏｒｏｃｙｔｏｐｈａｇａＢ２９）染色体用ＰｓｔＩ部分酶切后，连接到大肠杆菌（Ｅ．ｃｏｌｉ）质粒载体ｐＵＣ８上，然后转化Ｅ．ｃｏｌｉＪＭ８３，从而建立了Ｂ２９的基因文库，并筛选一个含有内切葡聚糖纤维素酶（ＣＭＣａｓｅ）的阳性克隆．从此阳性克隆中提取质粒再转化ＪＭ８３，发现所有的氨苄青霉素抗性（Ａｐｒ）转化子都具有ＣＭＣａｓｅ酶活性，证明在大肠杆菌中克隆到一个Ｂ２９的内切葡聚糖酶基因．

稳定性核素~(15)N在农业研究中的应用

稳定性核素示踪是现代农业研究中一门新兴技术。稳定性核素15N作为一种有效手段在农业施肥研究、氮素循环研究中发挥着极为重要的作用。本文介绍了15N的相关概念,列举了20世纪80年代以来15N在氮肥研究、氮素转化研究以及农业环境保护中的应用进展,阐明了应用15N的新技术已解决的问题,以及将要解决的问题,并展望了性核素示踪技术的应用前景。

抑制剂及其组合对尿素~(15)N在小麦土壤系统中的行为和归宿的影响

应用加有脲酶抑制剂 (HQ)、硝化抑制剂 (DCD)及其组合的标记尿素进行春小麦盆栽试验 .结果表明 ,在生长季节结束时 ,小麦回收 ,土壤残留和损失的肥料N各占施入N量的 1 7.65～ 2 3.69%、43.72～ 56.32 %和 1 9.99～ 36.77% .其中 ,与单施尿素相比 ,两种抑制剂配合使用处理的肥料N总回收率高 1 6.78% ,小麦回收高 5.96% .施用氮肥对籽粒贡献最大 ,占吸收肥料N量 43.3～ 62 .0 % .

植物油增塑聚苯乙烯包膜肥料的研究

目的为了提高化肥的利用率,降低缓释肥料的生产成本.方法以废弃聚苯乙烯泡沫塑料为基本材料、植物油为增塑剂对尿素进行包膜,用乙酸乙酯、乙酸乙酯和甲苯两种体系的溶剂进行溶解,制备包膜肥料.用水中溶出率法和土壤淋溶法研究包膜尿素控释效果.结果表明植物油对聚苯乙烯具有良好的增塑性,采用乙酸乙酯、乙酸乙酯和甲苯两种体系的溶剂进行溶解制备包膜肥料,除A1外,其他5种肥料初期溶出率均低于40%,可以确认用此两种体系溶剂溶解聚苯乙烯皆可行,混合溶剂体系的效果更好些.该包膜肥料的包膜量以10%为最佳.结论利用了聚苯乙烯废弃物,在一定程度上减少了"白色污染",同时又提高了尿素的利用率.综合利用资源、变废为宝、实现可持续性的循环经济发展.

近15年海南岛林地资源时空动态特征及政策驱动

遥感(RS)和地理信息系统(GIS)技术的发展为林地资源的调查和时空变化分析提供了有效手段。该文在遥感与地理信息系统技术支持下,利用中国资源环境数据库中1985年、1995年和2000年3期林地类型空间分布数据,通过建立林地资源时空演变模型,对海南岛林地资源变化的时空特征进行了定量分析,结果表明:1985年～2000年15年内,海南岛林地发生了大幅度的变化,而且空间差异非常明显,其中最近5年林地变化的广度和深度都远远超过了前10年。1985年～1995年海南岛林地资源总量出现大幅度增加,尤其是有林地的增长特别明显;而1995年～2000年大量的林地转为耕地和城镇建设用地,该时期有林地、灌木林和疏林地都出现大幅度减少。从空间格局来看,海口市在整个15年内,林地的变化始终最为突出,东部沿海县市,如文昌、琼海、万宁、陵水、保亭等林地变化的动态度和减少的数量都远远大于其他地区。文章还进一步分析了政策因子对林地资源变化的影响。

Nitrogen-15 signals of leaf-litter-soil continuum as a possible indicator of ecosystem nitrogen saturation by forest succession and N loads

National Key Research and Development Program [2010CB833502]; National Natural Science Foundation of China [30600071, 40601097, 30590381]; Chinese Academy of Sciences [KZCX2-YW-432, O7V70080SZ, LENOM07LS-01]; GUCAS [O85101PM03]

Mo掺杂对高纯Ce_(1-x)Nd_xO_(2-x/2)(x=0.10,0.15)体系烧结温度及晶界电性能的影响

用柠檬酸硝酸盐法制备高纯Ce1-xNdxO2-x/2(x=0.10,0.15)固溶体,加入摩尔分数为5%的Mo,研究了Mo掺杂对烧结温度、结构及电性能的影响.通过X射线衍射、电感偶合等离子体和场发射扫描电镜等手段对氧化物进行了结构表征,采用交流阻抗谱测试其电性能.柠檬酸硝酸盐法制备的前驱体经1450℃烧结24 h得到致密度大于96%的陶瓷材料;加入5%Mo,在1250℃下烧结8 h即可达到理想的致密度(>95%).加入Mo在烧结过程中可加快晶界迁移,促进晶粒生长,显著提高了晶界电导率.在600℃时Ce0.85Nd0.15O1.925的晶界电导率为2.56 S/m,加入Mo后材料的电导率增加到5.62 S/m.

Ternary lanthanide (Er3+, Nd3+, Yb3+, Sm3+, Pr3+) complex-functionalized mesoporous SBA-15 materials that emit in the near-infrared range

The tertiary lanthanide complexes [Ln(hfth)(3)phen] (Ln=Er, Nd, Yb, Sm) and [Pr(tfnb)(3)phen] have been Successfully covalently attached in the ordered SBA-15 mesoporous materials via a functionalized 1,10-phenanthroline group 5-(N,N-bis-3-(triethoxysilyl)propyl)ureyl-1,10-phenanthroline (Phen-Si). The derivative materials [denoted as Ln(hfth)(3)phen-S15 and Pr(tfnb)(3)phen-S15; Ln=Er, Yb, Nd, Sm; hfth=4,4,5,5,6,6,6-heptafluoro-1-(2-thienyl)hexane-1,3-dionate; tfnb=4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedionate] were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and N-2 adsorption/desorption.

Blue-light emission of mesoporous SBA-15 covalently bonded with carbazole chromophore

Much attention has been paid to carbazole derivatives for their potential applications as optical materials. For the first time, the blue-light-emitting carbazole chromophore has been covalently bonded to the ordered mesoporous SBA-15 (The resultant hybrid mesoporous materials are denoted as carbazole-SBA-15) by co-condensation of tetraethoxysilane (TEOS) and prepared compound 3-[N-3-(triethoxyilyl)propyl]ureyl-9-ethyl-carbazole (denoted as carbazole-Si) in the presence of Pluronic P123 surfactant. The results of H-1 NMR and Fourier transform infrared (FTIR) reveal that carbazole-Si has been successfully synthesized.

Near-infrared emission from novel tris(8-hydroxyquinolinate)lanthanide(III) complexes-functionalized mesoporous SBA-15

A novel mesoporous material covalently bonded with 8-hydroxyquinoline (HQ) was synthesized (designated as Q-SBA-15). The 5-formyl-8-hydroxyquinoline grafted to.(3-aminopropyl)triethoxysilane, that is, alkoxysilane modified 8-hydroxyquinoline (Q-Si), was used as one of the precursors for the preparation of the Q-SBA-15 material. On the basis of the other function of the Q-Si of coordinating to lanthanide (Ln) ions, for the first time, the LnQ(3) complexes (Ln = Er, Nd, Yb) have been covalently bonded to the SBA-15 materials.

Palladium within ionic liquid functionalized mesoporous silica SBA-15 and its catalytic application in room-temperature Suzuki coupling reaction

Initially, pore walls of mesoporous silica SBA-15 with template were modified with chlorotrimethylsilane. Then imidazolium salts were similarly incorporated covalently in the inner pore walls of mesoporous silica SBA-15 albeit without the template. Finally, palladium salts were introduced into the pore channels of the previously processed mesoporous silica via electrostatic interaction. The resulting palladium catalysts demonstrated exceptional activity for the room-temperature Suzuki Coupling reaction in aqueous-organic mixed solvents and good recycling ability for at least 4-6 times.

The direct electrochemistry behavior of Cyt c on the modified glassy carbon electrode by SBA-15 with a high-redox potential

It is discovered that SBA-15 (santa barbara amorphous) can provide the favorable microenvironments and optimal direct electron-transfer tunnels (DETT) of immobilizing cytochrome c (Cyt c) by the preferred orientation on it. A high-redox potential (254 mV vs. Ag/AgCl) was obtained on glassy carbon (GC) electrode modified by immobilizing Cyt c on rod-like SBA-15. With ultraviolet-visible (UV-vis), circular dichroism (CD), FTIR and cyclic voltammetry, it was demonstrated that immobilization made Cyt c exhibits stable and ideal electrochemical characteristics while the biological activity of immobilized Cyt c is retained as usual.

Synthesis, Spectroscopic Properties, and Stabilities of Ternary Europium Complex in SBA-15 and Periodic Mesoporous Organosilica: A Comparative Study

Ternary europium complex Eu(tta)(3)phen was covalently bonded with the general mesoporous. material SBA-15 and SBA-15-type of periodic mesoporous organosilica (PMO) material via impregnation of Eu(tta)(3)center dot 2H(2)O into phen-S15 and phen-PMO, respectively, through a ligand exchange reaction. The parent materials of phen-S15 and phen-PMO were synthesized by co-condensation of tetraethylorthosilicate (TEOS) or 1,2-bis(triethoxysilyl)ethane (BTESE) and the functionalized chelate ligand 5-(N,N-bis(3-triethoxysilyl)propyl)ureyl-1,10-phenanthroline (phen-Si) in the presence of Pluronic P123 surfactant as template, which were confirmed by SEM, XRD, FTIR, Si-29 CP-MAS NMR, and N-2 adsorption measurements.

High proton conductive advanced hybrid membrane based on sulfonated Si-SBA-15

Composite membranes based on Sulfonated poly(ether ether ketone) (SPEEK) and sulfonated organically modified Si-SBA-15 (S-SBA-15) were investigated with the purpose of increasing the proton conductivity. The novelty of the composite membranes was attributed to two special structures and different ion exchange capacities (IEC) of S-SBA-15 fillers, which were embedded in membranes. The typical hexagonal channels array of S-SBA-15 was confirmed by XRD and TEM. The regular vermiculate and amorphous structures of the inorganic fillers were proved by SEM. Composite membranes were prepared through common solvent casting method. SEM images indicated that the inorganic filler with regular structure dispersed homogeneously in the composite membranes, but the amorphous filler caused an agglomeration phenomenon at the same loading content.

Direct electron transfer and electrocatalysis of glucose oxidase immobilized on glassy carbon electrode modified with Nafion and mesoporous carbon FDU-15

In this paper, it was found that glucose oxidase (GOD) has been stably immobilized on glassy carbon electrode modified with mesoporous carbon FDU-15 (MC-FDU-15) and Nafion by simple technique. The sorption behavior of GOD immobilized on MC-FDU-15 matrix was characterized by transmission electron microscopy (TEM), ultraviolet-visible (UV-vis), FTIR, respectively, which demonstrated that MC-FDU-15 could facilitate the electron exchange between the active center of GOD and electrode. The direct electrochemistry and electrocatalysis behavior of GOD on the modified electrode were characterized by cyclic voltammogram (CV) which indicated that GOD immobilized on Nafion and MC-FDU-15 matrices display direct, reversible and surface-controlled redox reaction with an enhanced electron transfer rate constant of 4.095 s(-1) in 0.1 M phosphate buffer solution (PBS) (pH 7.12).