The shape parameter of Liposomes and DNA-lipid complexes determined by viscometry utilizing small sample volumes

A minicapillary viscometer utilizing <0.5 ml of sample at a volume fraction of <0.1% is described. The calculated a/b of DPPC/DPPG multilamellar liposome was 1.14 as prolate ellipsoids and a/b of dioleoylpropyltrimethyl ammonium methylsulfate-DNA complex at a charge ratio of 4: 1 (+/-) was 3.7 as prolate ellipsoids or 4.9 as oblate ellipsoids. The deviation of shape from perfect sphere is thus expressed quantitatively in more than two significant figures. In these measurement, the necessary amount of DNA is <0.5 mg.

The study on a PVC membrane electrode for gemfibrozil

In this paper, a poly(vinyl chloride) (PVC) membrane electrode is prepared for gemfibrozil, 2, 2-dimethyl-5(2,5-xylyloxy) valeric acid, based on its ion pair complexes with hexadecyltrioctyl ammonium iodide (HTOA). The membrane composition of the electrode was optimized by using the sequential level elimination method for orthogonal experimental design. The electrode has a Nernstian response range from 2.5 X 10(-5) to 0.1 mol/l with an average slope of 55.3 mV/decade. The limit of detection is 7.1 X 10(-6) mol/l. The electrode responses were not affected by pH in the range 10.0-12.3. A Na2B4O7-Na2CO3 buffer of pH = 11.0 was selected as the background electrolyte solution for potentiometric measurements. The electrode was used for determining gemfibrozil in pharmaceutical preparations with satisfactory results.

水蚀条件下不同土壤氮素和有机质流失规律

人工模拟放水冲刷试验研究结果表明 ,随放水冲刷强度的增大 ,不同土壤硝态氮、铵态氮、有机质和全氮流失加剧 ,泥沙全氮和有机质富集程度减少 ;当给不同土壤施等量的硝酸铵时 ,发现随径流流失化肥的铵态氮和硝态氮分别占施入量的 0 .9%～ 3 .5 %和 8.2 %～ 19.7% ,硝酸铵主要随径流流失 ,以泥沙颗粒流失量甚微 ;土壤侵蚀、有机质和全氮流失量与 >2 0 μm团聚体相关系数分别为 -0 .893 5、-0 .792 8和 -0 .815 1,2 0 μm直径的团聚体是区分土壤有机质和全氮流失的标准

陕北中部丘陵区土壤肥力现状及提高土地生产力的途径

调查分析了延安宝塔区和安塞县 7个乡镇近三年来的粮食生产 ,肥料投入以及各土地类型的土壤肥力状况 ,表明 :投入的化肥中 ,氮肥以低浓度养分的碳铵为主 ,平均占肥料总量的 38.3% ,从施入土壤的 N、P、K养分来看 ,K比例很小 ,结构不合理。土壤肥力总体水平低 ,且不同土地类型差异大 ;由于各乡镇自然和经济状况的差异 ,土地投入量不同 ,从而导致粮食产量相差悬殊 ,并且年际波动大。提高土地生产力的有效途径是培肥土壤和大力推广农作物高产栽培技术

黄土区退果还耕对黑垆土硝态氮积累和迁移的影响

在黄土高原沟壑区王东沟小流域,针对塬面、梁地和坡地三种地形,分别选取了盛果期果园、老果园和退果还耕地等,研究了退果还耕条件下,三种地貌类型土壤剖面中水分含量变化及NO_3~--N、NH_4~+-N积累和迁移规律。结果表明,无论塬面、梁地或者坡地上,果园土壤水分含量显著降低(10%～14%);果园退耕后,土壤水分开始缓慢恢复。盛果期,塬面NO_3~--N峰值主要处于100—200 cm之间,退果还耕后,100 cm以上土层中NO_3~--N含量降低,100cm以下NO_3~--N积累量在增加,并且峰值不断向下移动。盛果期果园NO_3~--N积累量为631～3032 kg/hm~2;退果还耕地、老果园NO_3~--N积累量都显著高于盛果期果园。盛果期40%以上的NO_3~--N积累在100—200 cm土层,但退果还耕地上50%左右集中分布在200—300 cm土层。土地利用与管理方式的变化对NH_4~+-N分布特征的影响并不明显。

黄土高原典型土壤矿物固定态铵变化的南北差异

采集从北向南依次分布的干润砂质新成土(神木)、黄土正常新成土(延安)和土垫旱耕人为土(杨陵)等典型土壤剖面0—200 cm土层土样,通过测定土样全氮和矿物固定态铵,以阐明黄土高原典型区域土壤全氮和矿物固定态铵及二者比率随地理位置和土层的变异规律,为全面了解黄土高原土壤相对稳定氮库累积提供科学数据。结果表明,不同地理位置、不同土层全氮和矿物固定态铵含量存在显著差异。从南到北全氮和矿物固定态铵呈下降趋势,但各土壤全氮和矿物固定态铵的分布显著不同,全氮含量在0—60 cm随土层深度增加下降很明显,60—120 cm有一定下降,120 cm以下低而稳定。矿物固定态铵在全剖面上的分布比较均匀,随土层深度的变化差异不显著,不同土层间的差异基本在误差范围内,土垫旱耕人为土、黄土正常新成土和干润砂质新成土表层(0—10 cm)矿物固定态铵平均含量分别为215.80±7.45、165.80±8.73和146.50±1.83 mg/kg,表层以下(10—200 cm)平均含量分别为193.40±9.67、157.14±5.75和142.02±5.47 mg/kg。从地理位置分析,干润砂质新成土、黄土正常新成土和土垫旱耕人为土表层...

氮素形态和铁营养对玉米苗期生长及体内铁分布的影响

以玉米(Zea mays)品种‘豫玉-22’为材料,采用营养液培养方法,研究了低铁和正常供铁条件下供应不同形态氮素对玉米苗期生长及体内铁分布的影响。结果表明:(1)与低铁介质相比,常铁介质增加了各氮素处理玉米幼苗的株高、地上部干重、全株干重,降低了根冠比,其中硝态氮处理表现得尤其突出;与供应硝态氮(NO3--N)相比,增施铵态氮(1/2 NO3--N+1/2 NH4+-N,NH4+-N)能明显促进低铁介质中玉米生长,但在常铁介质下作用不明显。(2)相比于低铁介质,正常供铁显著提高了相应处理玉米新叶叶绿素含量及净光合速率;2种供铁介质中,NH4+-N处理的新叶叶绿素含量以及净光合速率均高于其它氮素处理。(3)相比于低铁介质,正常供铁处理总体上增加了玉米各部分活性铁含量和全铁含量,对NO3--N处理的新叶活性铁含量增加尤其明显;2种供铁介质中,NH4+-N均有利于提高新叶活性铁含量和植株地上部全铁含量。(4)玉米新叶活性铁含量不仅与其叶绿素含量显著正相关(r=0.979**),也与叶片净光合速率显著正相关(r=0.950**)。研究发现,供铁状况显著影响玉米新叶的叶绿素含量及其净光合速率且与供氮形态存在互作;供应...

设施条件下氮肥对大青菜硝酸盐及土壤矿质氮累积的影响

采用田间实验研究了施用氮肥对设施条件下大青菜生长发育和产量,以及对土壤硝酸盐含量累积分布的影响。结果表明,在施氮肥0~500 kg hm-2范围内,氮肥施用量越大,产量越高,但到达一定量时,便不能再促进产量的提高,反而会引起减产。土壤铵态氮含量随着土壤剖面向下不断下降,表层的铵态氮含量较高,土壤硝态氮含量在整个土壤剖面的分布变化较小,但也是从表层向下处于一种缓慢减少的趋势,铵态氮的累积主要集中在上部土壤剖面,硝态氮的累积分布在整个土壤剖面,土壤硝态氮含量随施肥量增加而增加;氮肥施用量对硝酸盐含量有很大影响。在施氮肥0~700kg hm-2范围内,氮肥施用量越多,大青菜硝酸盐含量越高。

Preparation and Characterization of BaLiF3:Er3+ Nanoparticles by the Hydrothermal Microemulsion Synthesized Method

Nanoparticles of BaLiF3:Er3+ were prepared from the quaternary microemulsions of Cetyltrim-Enthyl Ammonium Bromide (CTAB), n-butanol, n-octane, and water, using the hydrothermal-microemulsion technique. The complex fluorides were characterized by means of X-ray power diffraction, Environmental Scanning Electron Microscopy (ESEM), and fluorescence spectra.

Ring-Enlargement of Dimethylaminopropenoyl Cyclopropanes: An Efficient Route to Substituted 2,3-Dihydrofurans

A convenient and efficient synthesis of substituted dihydrofurans is developed via ring-enlargement of 1-dimethylaminopropenoyl-1-carbamoyl/benzoyl cycloproparres catalyzed by ammonium acetate in acetic acid with high regio- and stereoselectivity. Some of the newly synthesized substituted dihydrofurans are subjected to further synthetic transformation in the presence of NaOH (aq) in ethanol to afford the corresponding 5-aryl-2,3-dihydrofuro[3,2-c]pyfidin-4(5H)-ones in high yields.

Fixation of carbon dioxide into aliphatic polycarbonate, cobalt porphyrin catalyzed regio-specific poly(propylene carbonate) with high molecular weight

Cobalt porphyrin complex ((TPPCoX)-X-III) (TPP = 5, 10, 15, 20-Tetraphenylporphyrin; X = halide) in combination with ionic organic ammonium salt was used for the regio-specific copolymerization of propylene oxide and carbon dioxide. A turnover frequency of 188 h(-1) was achieved after 5 h, and the byproduct propylene carbonate was successfully controlled to below 1%, where the obtained poly(propylene carbonate) (PPC) showed number average molecular weight (M-n) of 48 kg/mol, head-to-tail content of 93%, and carbonate linkage of over 99%.

C-60 trianion-mediated electrocatalysis and amperometric sensing of hydrogen peroxide

Heterogeneous electrocatalytic reduction of hydrogen peroxide (H2O2) by C-60 is reported for the first time. C-60 is embedded in tetra octyl ammonium bromide (TOAB) film and is characterized by scanning electron microscopy and cyclic voltammetry. Electrocatalytic studies show that the trianion of C-60 mediates the electrocatalytic reduction of H2O2 in aqueous solution containing 0.1 M KCl. Application of such film modified electrode as an amperometric sensor for H2O2 determination is also examined.

Promoting carbonization of polypropylene during combustion through synergistic catalysis of a trace of halogenated compounds and Ni2O3 for improving flame retardancy

The effect of combination between a trace of halogenated compounds (such as ferric chloride and ammonium bromide) and Ni2O3 particles on the carbonization of polypropylene (PP) was investigated during combustion. The results showed a synergistic catalysis of combined halogenated compounds with Ni2O3 in promoting the formation of the residual char during combustion. The investigation on the promotion mechanism showed that halide radical releasing from halogen-containing additives worked as a catalyst to accelerate dehydrogenation-aromatization of degradation products of PR which promote the degradation products to form the residual char catalyzed by nickel catalyst.

Preparation of bioactive glass ceramic nanoparticles by combination of sol-gel and coprecipitation method

SiO2-CaO-P2O5 ternary bioactive glass ceramic nanoparticles were prepared via the combination of sol-gel and coprecipitation processes. Precursors of silicon and calcium were hydrolyzed in acidic solution and gelated in alkaline condition together with ammonium dibasic phosphate. Gel particles were separated by centrifugation, followed by freeze drying, and calcination procedure to obtain the bioactive glass ceramic nanoparticles. The investigation of the influence of synthesis temperature on the nanopartilce's properties showed that the reaction temperature played an important role in the crystallinity of nanoparticle. The glass ceramic particles synthesized at 55 degrees C included about 15% crystalline phase, while at 25 degrees C and 40 degrees C the entire amorphous nanopowder could be obtained.

Convenient Synthesis of Substituted Quinoxalines and 2H-Benzo[b][1,4]oxazines in Water

A facile and convenient synthesis method has been developed for substituted quinoxalines and 2H-benzo[b][1,4]oxazines from the reactions of alpha-bromoketones with benzene-1,2-diamine and 2-aminophenol, respectively, which were catalyzed by tetrabutyl ammonium bromide (TBAB) in aqueous basic media.