Control of cocklebur seed germination by nitrogenous compounds : Nitrite, nitrate, hydroxylamine, thiourea, azide and cyanide

Germination of non-dormant upper cocklebur (Xanthium pinsylvanicum Wallr.) seeds was stimulated by not only CS(NH2)2 but also NH2OH, KCN and NaN3. This stimulation was not via the enhancement of aerobic C2H4 production. NH2OH, KCN and NaN3 in certain concentrations promoted the initial growth of axial and/or cotyledonary parts, but the degree of growth promotion by NH2OH, NaN3 and KCN was slight compared with that by CS(NH2)2. As in the case of CS(NH2)2, however, the germinationstimulating effect of NH2OH disappeared rapidly as the preceding imbibition period was prolonged. In contrast, KCN and NaN3 were still effective in stimulating the germination of aged seeds maintained on a water substratum, as previously seen with anaerobiosis. Anaerobic induction was enhanced not only by NaN3 and KCN but also by NH2OH, KNO3, KNO2 CO(NH2)2 and CS(NH2)2 applied during the anaerobic treatment, but without causing an increase in anaerobic production of C2H4. Furthermore, KCN and NaN3, given prior to the anaerobic treatment acted additively with anaerobic induction. The germination-stimulating actions of nitrogenous compounds are discussed in comparison with those of C2H4 and anaerobiosis.

黄土塬区三种豆科牧草的竞争生长

通过田间试验研究了沙打旺、紫花苜蓿和达乌里胡枝子3种豆科牧草在黄土旱塬以不同密度单播、混播时的竞争生长能力及水分利用效率。单播时苜蓿生长次年3个密度的生产力分别为15349kg·hm-2、20582kg·hm-2、21531kg·hm-2,沙打旺和胡枝子3个密度的生产力分别为7979kg·hm-2、16 440 kg·hm-2、21055kg·hm-2和2412kg·hm-2、5270kg·hm-2、7102kg·hm-2。混播草地生产力以苜蓿+胡枝子最高(平均19227kg·hm-2),沙打旺与胡枝子混播的生产力最低(平均11977kg·hm-2)。和生产力较高的参混种苜蓿、沙打旺单播相比,苜蓿与沙打旺混播及沙打旺与胡枝子混播的生产力在3种密度下均有不同程度的降低。苜蓿主根下扎深度2m,0~60cm根系占总根量的66%,沙打旺和胡枝子根系最大下扎深度分别为1.8 m和1.5m,0~60cm根系占总根量比例分别是80%、91%。3种牧草中苜蓿的平均水分利用效率最高,为25.75kg·mm-1·hm-2,胡枝子最低为7.71kg·mm-1·hm-2,沙打旺居中。苜蓿群体种内个体间竞争强度高于沙打旺和胡枝子。结果...

磷素在土壤中的垂直迁移潜力研究

针对磷素在田间条件下是否可以发生垂直迁移存有的疑问,利用模拟土柱研究了渗漏液磷含量的变化特点。结果表明,淹水后土柱渗漏液中总磷、有机磷的变化基本上表现为逐渐升高而后有所降低的趋势;施磷肥和猪粪处理土柱渗漏液中的总磷量高于无磷肥处理;施猪粪处理土柱渗漏液中有机磷量明显高于施无机磷肥的处理。

农田和森林土壤中氧化亚氮的产生与还原(英文)

采用土壤淤浆方法对丹麦农田和山毛榉森林土壤反硝化过程中N2 O的产生与还原进行了研究 ,同时考察了硝酸根和铵离子对反硝化作用的影响 .结果表明 ,森林土壤反硝化活性大于农田土壤 ,但农田土壤中N2 O还原活性大于森林土壤 ,表现在农田和森林土壤中N2 O/N2 的产生比率分别为 0 .11和 3 .65 .硝酸根和铵离子能促进两种土壤中的N2 O产生 ,但可降低农田土壤中的N2 O还原速率 .与农田土壤相比 ,硝酸根可降低森林土壤N2 O的还原能力 ,而铵离子却表现出对N2 O还原的促进作用 .培养 1周内尽管农田土壤中硝酸根始终存在 ,但几乎所有产生的N2 O都被还原成N2 .然而 ,只有当硝酸根几乎耗尽 ,森林土壤中N2 O的还原才开始进行 .由于两种土壤 pH值的不同造成硝酸根对N2 O还原抑制作用的差异 ,因为酸性条件下硝酸根对N2O还原的抑制较强 .因此 ,土壤消耗大气N2 O的适宜条件为厌氧 ,pH中性和硝酸根含量低 .

New carbazole-based copolymers as amorphous hole-transporting materials for multilayer light-emitting diodes

New carbazole-based copolymers, which contain various concentrations of 9-alkyl-3, 6-carbazole fragments in the main chain connected via alkylene spacers, have been synthesized by Ni(0)-catalyzed Yamamoto-type aryl-aryl coupling reactions. Full characterization of the copolymer structure by NMR spectroscopy and elemental analysis is presented. These compounds represent amorphous materials of high thermal stability with glass transition temperatures of 151-162 degrees C and thermal decomposition starting at temperatures > 390 degrees C. UV-Vis absorption and photoluminescence emission of the copolymers confirmed that the effectively conjugated segment in the 3,6-linked carbazole-type copolymers is limited to dyads (dimeric units). However, copolymers with varying concentrations of the oligocarbazole chromophores demonstrate different charge injection and transport properties in multilayer light-emitting diodes with the copolymers as the hole transport and Alq(3) as the electroluminescent/electron transport layer. The device based on a copolymer composed of oligocarbazole blocks with an average length of around four carbazoles exhibited the best overall performance with a turn-on voltage of 3.5 V, a maximal photometric efficiency of 4.1 cd center dot A(-1) and maximum brightness of about 4 200 cd center dot m(-2).

Fabrication, patterning and luminescence properties of X-2-Y2SiO5 : A (A = Eu3+, Tb3+, Ce3+) phosphor films via sol-gel soft lithography

X-2-y(2)SiO(5):A (A = Eu3+, Tb3+, Ce3+) phosphor films and their patterning were fabricated by a sol-gel process combined with a soft lithography. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), atomic force microscopy (AFM), scanning electron microscopy (SEM) optical microscopy and photoluminescence (PL) were used to characterize the resulting films. The results of XRD indicated that the films began to crystallize at 900 degreesC with X-1-Y2SiO5, which transformed completely to X-2-Y2SiO5 at 1250 degreesC. Patterned thin films with different band widths (5 pin spaced by 5 pm and 16 pm spaced by 24 pm) were obtained by a soft lithography technique (micromoulding in capillaries, MIMIC). The SEM and AFM study revealed that the nonpattemed phosphor films were uniform and crack free, and the films mainly consisted of closely packed grains with an average size of 350 run. The doped rare earth ions (A) showed their characteristic emissions in X-2-Y2SiO5 phosphor films, i.e., D-5(0)-F-7(J) (J = 0, 1, 2,3,4) for Eu3+, D-5(3), (4)-F-7(J) (J = 6, 5, 4, 3) for Tb3+ and 5d (D-2)-4f (F-2(2/5),(2/7)) for Ce3+, respectively. The optimum doping concentrations for EU3+, Tb3+ were determined to be 13 and 8 mol% of Y3+ in X-2-Y2SiO5 films, respectively.

Novel two-dimensional sodium molybdenum phosphates containing {M(enMe)(2)}(2+) bridging groups (M = Ni, Cu; enMe=1,2-diaminopropane)

Two novel organic-inorganic hybrid compounds, (H(2)enMe)(4)(H3O)[Ni(enMe)(2)].[Na3Mo12O52P8(OH)(10)].5H(2)O (1) and (H(2)enMe)(4)(H3O)[Cu(enMe)(2)].[Na3Mo12O52P8(OH)(10)].5H(2)O (2) (enMe = 1,2-diaminopropane), have been hydrothermally synthesized and characterized by elemental analyses, IR, EPR, XPS, UV-Vis spectra and TG analyses. Single crystal X-ray diffraction shows that 1 and 2 are isostructural compounds. Both the compounds exhibit an unusual two-dimensional (2-D) window-like network consisting of one-dimensional (1-D) chains of sodium molybdenum phosphate anions connected by transition metal coordination complexes cations. Compound 1 and 2 represent the first 2-D molybdenum phosphate skeleton pillared by transition metal complex fragments.

Hydrothermal synthesis, structure, and characterization of two one-dimensional chainlike hybrid complexes [(CuX)(2)(o-phen)](infinity) (X = Br, Cl; o-phen = o-phenanthroline)

Two novel organic-inorganic hybrid complexes [(CuX)(2)(o-phen)](infinity) (X = Br (1), Cl (2); o-phen = o-phenanthroline) have been synthesized hydrothermally and characterized structurally by elemental analyses, IR, ESR, XPS spectrum, TG analyses and single-crystal X-ray diffraction. Both title compounds exhibit novel one-dimensional chainlike copper halide scaffolding constructed by the unusual [Cu3X3] hexagon motifs by sharing opposite edges, where a single Cu site of each [Cu3X3] hexagon is chelated with N donors of o-phen group. To our knowledge, such basic o-phen-copper halide skeleton has not been reported hitherto. Moreover, TG analyses indicate that both title compounds possess high thermal stability.

Study on the structure change and oxygen vacation shift for Ce1-xSmxO2-y solid solution

A series of solid electrolytes Ce1-xSmxO2-y (x=0similar to0.6) were prepared by sol-gel method. XRD measurement showed that single-phase solid solution was formed in all investigated ranges at 160 degreesC, which is a significantly lower synthesis temperature compared to traditional solid state reaction. High temperature X-ray, ESR, and Raman scattering were used to characterize the samples. ESR measurement showed that ESR with sample irradiated by high-energy particle is an effective way to study the defect structure. These changes in the Raman spectrum are attributed to O vacancies, which are introduced into the lattice when tetravalent Ce4+ is substituted by trivalent Sm3+.

有机氨钙催化聚合脂肪族环酯

分别用经环氧丙烷和环氧丙烷/乙腈处理的氨钙催化剂催化聚合了ε-己内酯和L-丙交酯.研究了催化剂浓度、聚合时间、真空度、聚合温度和陈化温度等对聚合收率和聚合物粘均分子量的影响.结果表明,有机氨钙催化剂对ε-己内酯和 L-丙交酯的开环聚合有较高的催化活性 ,在较低的温度下和较短的时间内,即可获得较高的转化率和较高的分子量 ,而且具有一些“准活性聚合”的特点,分子量在一定范围内可控.陈化处理和乙腈的加入可以大大提高聚ε-己内酯的分子量 ,最大分子量达到27×104.

Gd3+ -> Eu2+ energy transfer in BaLiF3 : Eu, Gd

Photoluminescence characteristics and the energy transfer between Gd3+ and Eu2+ in BaLiF3,, matrix have been investigated. A series of concentrations of Gd3+ ion with a fixed Eu2+ concentration doped in BaLiF3 : Gd3+, Eu2+ has been studied. When the doping concentration for Gd3+ was 0.3%,, the system reached the highest energy transfer efficiency. Due to the competitive absorption for the Gd3+ and the Eu2+ ions in BaLiF3 : Gd3+ : Eu2+, when the doping concentration for Gd3+ ion exceeded 0.3 Vo, the continuously increasing concentration of Gd3+ ions caused the competitive absorption ratio for Gd3+ increasing and the emission intensity of Eu2+ decreasing. The energy transfer processes were discussed, while the transfer probability was calculated to be 1.35 X 10(5) s(-1).

BaLiF_3∶Eu,Gd中Gd~(3+)→Eu~(2+)的能量传递

研究了 Ba Li F3中 Gd3+和 Eu2 +的光谱性质及 Gd3+对 Eu2 +的能量传递过程 ,讨论了传递机理 .Gd3+的含量 (物质的量分数 )为 0 .3 %时 ,传递效率最高 ,传递几率 PSA=1 .3 5× 1 0 5s- 1 .当 Gd3+的含量高于 0 .3 %时 ,由于 Gd3+ 和 Eu2 + 竞争吸收 Gd3+ 占优势 ,增加 Gd3+ 含量 ,竞争吸收比相应增加 ,Eu2 + 自身吸收光子数目减少 ,发射强度降低

Johnson-Segalman流体剪切流动的相平面分析与数值模拟

研究Johnson-Segalman流体的剪切流动行为.首先分析该模型的定常解,从稳定的总剪切应力曲线上可见,当稳定总剪切应力T取值足够大或足够小时,方程有惟一定常解;当T取中间值时,方程定常解不惟一.最后,采用向后差分格式对该模型进行数值模拟.

Zn_2SiO_4∶Mn的VUV和UV光谱特性

采用高温固相反应法以硅酸为原料合成了等离子显示用荧光体Zn2 SiO4 ∶Mn ,研究了Zn2 SiO4 ∶Mn的VUV和UV光谱特性 ,表明波长小于 2 0 0nm的部分的基质吸收带主要是氧的 2 p轨道到锌的 3d轨道跃迁产生的 ,波长大于 2 0 0nm的部分的基质吸收带是氧的 2 p轨道到硅的 3p轨道跃迁吸收。在VUV和UV激发下 ,Mn2 +的浓度与发射强度的相关性研究表明 ,在不同区域激发时荧光体的发射强度随着Mn2 +的浓度的变化存在明显不同