Thermochemical and thermal analysis on N-(p-methylphenyl)-N '-(2-pyridyl)urea

Low temperature heat capacities of N-(p-methylphenyl)-N'-(2-pyridyl)urea were determined by adiabatic calorimetry method in the temperature range from 80 to 370 K. It was found that there was not any heat anomaly in this temperature region. Based on the experimental data, some thermodynamic function results were obtained. Thermal stability and decomposition characteristics analysis of N-(p-methylphenyl)-N'-(2-pyridyl)urea were carried out by DSC and TG. The results indicated that N-(p-methylphenyl)-N'-(2-pyridyl)urea started to melt at ca. 426 K (153degreesC) and the melting peak located at 447.01 K (173.86degreesC). The melting enthalpy was 204.445 kJ mol(-1) (899.6 J g(-1)). The decomposition peak of N-(p-methylphenyl)-N'-(2-pyridyl)urea was found at 499.26 K (226.11degreesC) from DSC curve. This result was similar with that from TG and DTG experiment, in which the mass loss peak was determined as 500.4 K (227.2degreesC).

Determination of urinary oxidative DNA damage marker 8-hydroxy-2 '-deoxyguanosine and the association with cigarette smoking

8-hydroxy-2'-deoxyguanosine (8OHdG) has been widely used as a biomarker of oxidative DNA damage in both animal models and human studies. To evaluate the effect of cigarette smoking on oxidative stress, we studied the levels of urinary 8OHdG from smokers and non-smokers and investigated the association with cigarette smoking. The urinary 8OHdG concentrations were determinated by capillary electrophoresis with end-column amprometric detection (CE-AD) after a single-step solid phase extraction (SPE), and then quantitatively expressed as a function of creatinine excretion. To increase the concentration sensitivity, a dynamic pH junction was used and the focusing effect was obvious when using 30 mM phosphate (pH 6.50) as sample matrix. The limit of detection is 4.3 nM (signal-to-noise ratio S/N = 3). The relative standard deviation (R.S.D.) was 1.1% for peak current, and 2.3% for migration time. Based on the selected CE-AD method, it was found that the mean value of urinary 8OHdG levels in the smokers significantly higher than that in non-smokers (31.4 +/- 18.9 nM versus 14.4 +/- 7.6 nM, P = 0.0004; 23.5 +/- 21.3 mug g(-1) creatinine versus 12.6 +/- 13.2 mug g(-1) creatinine, P = 0.028). (C) 2004 Elsevier B.V. All rights reserved.

不同AM真菌对三叶草耐油性的影响

在盆栽条件下研究了 4个油浓度 ( 0、5 0 0 0、10 0 0 0和 5 0 0 0 0w /mgkg-1)下接种由辽河油田油污染土壤中分离出的 3种AM真菌 (Glomusmosseae ,G .geospora ,G .constrictum )对三叶草耐油性的影响 .试验结果表明 :1)随着油浓度的增加 ,侵染率亦增加 ,10 0 0 0mgkg-1时G .geospora和G .constrictum的侵染率分别为 6 7.6 5 %和 82 .86 % ;2 )从侵染率、地上部生物量和菌根依赖性来看 ,随着油浓度的增加 ,最适的AM真菌亦不一样 .油浓度为 0、50 0 0和 10 0 0 0mgkg-1时 ,最适AM真菌分别是G .geospora、G .mosseae和G .constrictum ;3)油污染土壤上接种AM真菌能促进植株的地下部和地上部的生长 ,接菌处理的茎干重比相应的对照增加 6 2 .2 %～ 2 6 7.1% ;4)随着油浓度的增加和植物的生育进程 ,AM真菌的接种效应在增强 .图 3表 3参 14

丁香幼胚离体培养及组织快繁(英文)

利用正交试验进行了丁香的幼胚离体培养和增殖培养两方面的研究,对基本培养基、糖浓度、谷氨酰胺浓度、BA浓度、NAA浓度都进行了仔细的筛选。结果表明:幼胚培养的最适胚龄为50天;幼胚培养所需要的最适培养基为附加BA(0.1mg稬-1)、NAA(0.001mg稬-1),糖50(g稬-1),Gln(400mg稬-1)的Monnier培养基,幼胚萌发率可达91.7%;Gln的加入对幼胚培养有显著影响。此外,丁香实生苗最适的增值培养基为MS+BA(2mg稬-1)、NAA(0.01mg稬-1)、IBA(0.5mg稬-1)、Gln(100mg稬-1),此时繁殖系数大于3.6,可以满足生产需要。图1表7参8。

Novel activity of TiO2 for catalytic conversion of CO and H2O to alcohols in the presence of K2CO3

In the presence of K2CO3, TiO2 shows good catalytic activity and stability for the alcohols synthesis from CO and H2O. CO conversion of 7.6% and the STY of MeOH (about 24 mg g(-1) h(-1)) and EtOH (about 8 mg g(-1) h(-1)) are obtained under reaction conditions of T = 573 K, P = 0.5 MPa, CO flow rate of 30 ml min(-1) and CO/H2O = 3/2 during the period of 12 h to 44 h time-on-stream.

The Early Diagenetic Formation of Organic Sulfur in the Sediments of Mangrove Lake, Bermuda

Due to a low mineral content, the sapropelic sediments depositing in Mangrove Lake, Bermuda, provide an excellent opportunity to explore for possible additions of sulfur to organic matter during the early stages of diagenesis. We evaluated early diagenetic organic sulfur transformations by monitoring the concentrations and stable isotopic compositions of a number of inorganic and organic sulfur pools, thereby accounting for all of the sulfur in the sediments. We have identified and quantified the following sulfur pools: porewater sulfate, porewater sulfide, elemental sulfur, pyrite sulfur, hydrolyzable organic sulfur (HYOS), chromium-reducible organic sulfur (CROS), and nonchromium-reducible organic sulfur (Non-CROS). Of the organic sulfur pools, the Non-CROS pool is by far the largest, followed by CROS, and finally HYOS. By 60 cm depth these pools contribute, respectively, to 85, 7.9, and 3.6% of the total solid phase sulfur. The HYOS pool is probably of biological origin and shows no interaction with the sulfur compounds produced during diagenesis. By contrast, CROS is produced, most likely, from the diagenetic addition of polysulfides to functionalized lipids in the upper, H2S-poor, elemental sulfur-rich, region of the sediment. A portion of this sulfur pool is unstable and decomposes on contact with the H2S-rich porewaters. The portion of CROS that remains in the sulfidic waters appears to readily exchange sulfur isotopes with H2S. While some of the Non-CROS pool is of biological origin, some is also formed by the diagenetic addition of sulfur to organic compounds in the upper H2S-poor region of the sediment. By contrast with CROS, Non-CROS is not diagenetically active in the H2S-rich porewaters. Overall, somewhere between 27 and 53 % of the organic sulfur buried in Mangrove Lake sediments is of diagenetic origin, with the remaining organic sulfur derived from biosynthesis. We extrapolate our Mangrove Lake results and calculate that in typical coastal marine sediments between 11 and 29 μmol g−1 of organic sulfur will form during early diagenesis, of which 2–5 μmol g−1 will be chromium reducible.

石油污染土壤长料堆式异位生物修复技术研究

应用长料堆式处理技术在长 2 0m、宽 10m的实用规模预制床上对辽河油田不同类型原油污染土壤进行了处理 .处理工程设 8个长条状堆料单元 ,每个堆料单元长 8m、宽 2m、高 0 .35m .当稀油、稠油和高凝油污染土壤中石油烃总量 (TPH)为 4.16～ 7.72 g·10 0 g-1土时 ,经过 5 3d的运行 ,TPH去除率 45 .19%～ 5 6 .74% .本研究为石油污染土壤异位生物修复实用化提供了技术支持 .

石油污染土壤堆制微生物降解研究

采用异位生物修复技术堆式堆制处理方法 ,对辽河油田原油污染土壤进行了生物修复处理研究 .处理工程设 4个处理料堆单元 ,每个处理单元长 118.5cm ,宽 6 5 .5cm ,高 12 .5cm .研究结果表明 ,当进行处理的石油污染土壤中石油烃总量为 5 .2 2 g·10 0 g-1土时 ,利用黄孢原毛平革菌 (Phanerochaetechrysospori um) ,经过 5 5d的运行 ,石油烃总量去除率达 5 4.2 % .堆制处理中影响污染土壤石油烃总量生物降解的主要变化因子为污染土壤的O2 和CO2 含量、降解石油烃微生物的数量、污染土壤pH的变化 .通过监测这些数据的变化 ,可直接反映该工程的处理石油污染土壤的效果 .本处理工程采用定期通风措施 ,操作简单、运行费用低廉 ,为石油污染土壤生物修复实用化提供了一种简单易行的污染土壤清洁技术 .

利用比较染色体涂色和BAC定位技术探讨麂属动物染色体的起源和演化

比较细胞遗传学研究发现物种的形成过程往往伴随着核型结构的变化，各种鹿属动物染色体的巨大差异正是很好的例证'赤魔的染色体被证明是由具有端着丝粒的祖先染色体经过多次的串联融合进化而来的。根据祖先染色体的形态和连接方式，可以将染色体串联融合主要分为三类：着丝粒一着丝粒融合，着丝粒一端粒融合和端粒一端粒融合。经典细胞遗传学，比较染色体涂色，卫星DNA序列和部分融合位点序列比较研究都支持串联融合假说。但串联融合的类型和分子机制迄今没有完全弄清楚。本论文旨在对魔属动物的串联融合类型和分子机制进行研究，分为两个部分：一、通过比较染色体涂色的方法，建立小鹿一林察一大额牛的比较染色体图谱，结合以前发表的结果来阐明鹿科（小魔）与牛科（大额牛），寮科（林磨）之间的核型关系；二、建立赤鹿的全基因组BAc文库，通过克隆定位的方法确立在赤魔的染色体进化过程中所发生的串联融合类型，并对其机制进行探讨。主要结果如下：利用小鹿的染色体特异探针与林寮，大额牛的染色体进行杂交，首次建立了小鹿一大额牛，小魔一林察的核型对比关系。结果显示小鹿的1-5、11号染色体均与林集和大额牛的多段染色体同源。结合高分辨的G带比较，发现小魔1-5和11号染色体上的与林爵和大额牛对应的所有同源片断在小鹿染色体上呈着丝粒一端粒连接排列。从而进一步证明小鹿的1-5和11号染色体是由2n=70的祖先核型通过染色体的着丝粒一端粒串联融合方式进化而来的。建立了我国第一个赤魔全基因组BAC文库，该文库由124800个克隆组成。大部分插入片段的大小在100-145kb之间，片段的平均大小为12＜0kb。克隆定位显示克隆的分布与小鹿染色体大小成正比关系，说明整个文库没有染色体的偏倚，文库为整个基因组的6倍，覆盖率几乎为100％。通过赤鹿BAC克隆在小魔和赤鹿染色体上的精确定位，使我们得以准确判断小鹿染色体在赤鹿染色体同源片段上的连接方式，并确定串联融合的类型。结果进一步支持赤鹿的核型是由一个2n=70祖先核型通过着丝粒一端粒的融合方式进化而来的。

Energy transfer from Tb3+ to Mn2+ in LaMgAl11O19:Tb, Mn phosphors

Luminescent properties of LaMgAl11O19:Tb, Mn phosphors were investigated. It was observed that the energy distributions of the Tb3+-emission bands associated with transitions from the D-5(3) and D-5(4) levels to F-7(J) depend on the Tb3+-concentration, which is due to the cross-relaxation between Tb 31 ions. The emission band at about 516 nm is attributed to the T-4(1) -> (6)A(1) transition of the Mn2+ ions. We observed an energy transfer from the Tb 3, to Mn2+ ions in LaMgAl11O19:Tb, Mn.

Nd~(3+)掺杂对LiFePO_4结构及电化学性能的改善

采用两步加热高温固相法合成了掺杂Nd3+的LiFe1-xNdxPO4/C复合材料(x=0,0.01,0.02,0.04,0.06,0.08)。用TG-DSC对前驱体进行分析和SQUID(超导量子干涉仪)对样品中Fe3+的磁性测定,优化了合成工艺条件;采用XRD、FE-SEM、EDS等方法分析了样品的结构并对其电化学性能进行了测试。结果表明:LiFe1-xNdxPO4/C复合材料具有橄榄石型结构;当Nd3+的掺杂量6%(物质的量分数)、煅烧温度700℃、煅烧时间16 h时,样品在0.2C(1C=170.0 mA.g-1)电流密度下的最大放电比容量可达165.2 mAh.g-1,循环100次后的容量保持率仍为92.8%,在1C、2C、5C下的最大放电比容量分别为146.8、125.7和114.8 mAh.g-1。通过测定样品在不同较低倍率下的放电比容量,采用外推法得出制备样品的实测理论比容量为168.7 mAh.g-1。

Novel proton exchange membranes based on water resistant sulfonated poly[bis(benzimidazobenzisoquinolinones)]

Novel water resistant sulfonated poly[bis(benzimidazobenzisoquinolinones)] (SPBIBIs) were synthesized from 6,6'-disulfonic-4,4'-binaphthy]-1,1',8,8'-tetracarboxylic dianhydride (SBTDA) and various aromatic ether tetraamines. The resulting polymers with IEC in the range of 2.17-2.87 mequiv g(-1) have a combination of desired properties such as high solubility in common organic solvents, film-forming ability, and excellent thermal and mechanical properties. Flexible and tough membranes, obtained by casting from m-cresol solution, had tensile strength, elongation at break, and tensile modulus values in the range of 87.6-98.4 MPa, 35.8-52.8%, and 0.94-1.07 GPa. SPBIBI membranes with a high degree of sulfonation displayed high proton conductivity and a good resistance to water swelling as well. SPBIBI-b with IEC of 2.80 mequiv g(-1) displayed the conductivity of 1.74 x 10(-1) S cm(-1) at 100 degrees C, which was comparable to that of Nafion (R) 117 (1.78 x 10(-1) S cm(-1), at 100 degrees C).

Direct synthesis of ordered N-methylimidazolium functionalized mesoporous silica as highly efficient anion exchanger of Cr(VI)

Ordered N-methylimidazolium functionalized mesoporous silica (SBA-15) anion exchangers were directly synthesized by co-condensation of tetraethoxysilane with 1-methyl-3(triethoxysilylpropyl)imidazolium chloride. The prepared samples with rod-like morphology showed high surface areas (> 400 m(2) g(-1)), well-ordered pores (> 58 angstrom), and excellent thermal stability up to 387 degrees C. The adsorption behaviors of Cr(VI) from aqueous solution on the anion exchangers were studied using the batch method. The anion exchangers had high adsorption capacity ranging from 50.8 to 90.5 mg g(-1), over a wider pH range (1-8) than amino functionalized mesoporous silica. The adsorption rate was fast, and the maximum adsorption was obtained at pH 4.6. The adsorption data for the anion exchangers were consistent with the Langmuir isotherm equation. Most active sites of the anion exchangers were easily accessible. The mixed solution of 0.1 mol L-1 NH3 center dot H2O and 0.5 mol L-1 NH4Cl was effective desorption solution, and 95% of Cr(VI) could be desorbed.

Structure and electrochemical characteristics of TiV1.1Mn0.9Nix (x=0.1-0.7) alloys

The structure and electrochemical properties of TiV1.1Mn0.9Nix (x = 0.1-0.7) solid solution electrode alloys have been investigated. It is found that these alloys mainly consist of a solid solution phase with body centered cubic (bcc) structure and a C14 Laves secondary phase. The solid solution alloys show easy activation behavior, high temperature dischargeability, high discharge capacity and favorable high-rate dischargeability as a negative electrode material in Ni-MH battery. The maximum discharge capacity is 502 mAh g(-1) at 303 K when x = 0.4. Electrochemical impedance spectroscopy (EIS) test shows that the charge-transfer resistance at the surface of the alloy electrodes decreases obviously with increasing Ni content.