偶氮氯膦-mA(CPA mA)离解作用的研究

本文用pH电位法和分光光度法研究了偶氮氯膦-mA的六级离解作用,测定了其逐级电离常数,计算了离解过程的热力学参数△G°、△H°、△S°,同时与对硝基偶氮氯膦的离解常数进行了比较,其结果与量子化学计算基本相符。

DBC-偶氮胂在水溶液中离解作用的研究

3-(2-胂酸基苯偶氮-6-(2,6-二溴-4-氯苯偶氮)-4,5-二羟基-2,7-萘二磺酸)(简称DBC-偶氮胂)可在高酸度下(0.2-1.7NHCl)与稀土元素发生灵敏显色反应,且选择性非常好,前文已报导用该试剂直接光度测定高温合金中微量铈。本文研究了DBC-偶氮胂在水溶液中的离解作用,用pH电位法及分光光度法测定DBC-偶氮胂及各级条件离解常数,结果表明:由于多卤素原子的引入,使试剂更易于质子化;因而离解常数比偶氮胂Ⅲ大。

三氯偶氮胂的提纯、鉴定及其在水溶液中的离解作用研究

建立了三氯偶氮胂的萃取提纯方法,纯品经色层分析、红外光谱分析、元素分析以及有效成分测定,均表明有效成分达95%以上.用分光光度法测定了三氯偶氮胂的六级离解常数,而且探讨了该试剂在高酸度下与金属离子显色反应的反应机理.

1-氨基乙叉-1,1-二膦酸离解作用的研究

用pH电位法研究了AEDP的五级离解常数 ,计算了离解过程的热力学参数ΔG0 、ΔH0 、ΔS0 .

飞秒激光对离体兔巩膜的光离解作用

为探索飞秒激光在兔眼巩膜上产生光离解作用的可行性，并寻找适当的激光切割方式及相关参数，将不同脉冲能量的飞秒激光（800nm／50fs）聚焦后作用于离体兔眼巩膜。通过计算机控制的三维平台的定向移动，飞秒激光能够在兔眼巩膜上完成打孔、蛇形扫描和线性切割三种方式的光离解作用。应用光学显微镜和扫描电镜（SEM）观察激光作用后巩膜的形态学变化，并用Nd：YAG激光作为对比。实验结果表明，飞秒激光经过显微物镜（NA：0．2）聚焦后，当其功率密度达到或超过9．55×10^14W／cm^2，脉冲能量在37．5～125M变化时，激光以0．1mm／s的速度线性扫描巩膜能形成深度为30～70μm的沟道；当激光的功率密度减小至7．96×10^14W／cm^2，脉冲能量小于31．25μJ／pulse时，在相同条件下却不能产生光离解作用。与Nd：YAG激光相比，飞秒激光在兔眼巩膜上切割瘘道的内壁更加光滑整齐，对周围的组织损伤更小。飞秒激光对离体兔眼巩膜高精度和微创伤的光离解作用，预示了它在未来青光眼治疗中有潜在的应用价值。

均三溴氯磺酚离解与质子化作用的研究

本文报道测钪新试剂均三溴氯磺酚在水溶液中的离解与质子化作用,用电位法和光度法测得了它的逐级离解常数与质子化常数,以及热力学参数,并由分布函数获得试剂主要存在形式和pH值的关系。

3.7A GeV^(16)O-Em作用α射弹碎片多重数分布

对3.7AGeV16OEm作用产生的α射弹碎片多重数分布进行了研究,得出电磁离解作用和核作用下α射弹碎片的分布服从不同的函数,说明在两种作用下碎片的产生机制不同.

酚酞—酸碱指示剂的讨论

在全国统编初中化学教材酸的通性和碱的通性中有这样的提法:“无色的酚酞遇酸溶液不变色,无色的酚酞遇碱液溶变红色”.作者认为上述两句话不够确切,值得商榷.我们知道,酚酞指示剂是弱的有机酸,它在水溶液中发生如下的离解作用和颜色的变化.

Enantioselective Degradation of Rac-Metolachlor and S-Metolachlor in Soil

Separation of chiral enantiomers and the dissipation of rac-metolachlor and S-metolachlor in soil were evaluated using achiral high-performance liquid chromatography (HPLC) and chiral gas chromatography (GC) methods. Under the experimental conditions the possible metabolite was considered to be N-(2-ethyl-6-methyl-phenyl)-2-hydroxy-acetamide. Because of the presence of two chiral elements (asymmetrically substituted carbon and chiral axis), the baseline separation of metolachlor enantiomers was not achieved. S-metolachlor degraded faster in soil than rac-metolachlor. After a 42-day incubation, 73.4% of rac-metolachlor and 90.0% of S-metolachlor were degraded. However, due to the absence of biological processes the degradation process in sterilized soil showed no enantioselectivity. The results indicated that enantioselective degradations could greatly affect the environmental fate of metolachlor and should be considered when the environmental behavior of these compounds was assessed.

A Velocity Map Ion-imaging Study on Ketene Photodissociation at 218 nm

Photodissociation dynamics of ketene at 218 nm has been investigated using the velocity map ion-imaging method. Both angular and translational energy distributions for the CO products at different rotational and vibrational states have been obtained. The 2＋1 REMPI spectrum of CO products is also obtained. The results are as bellow： （i） CO products in the first two vibrational states （ v＂=0 and v＂=1 ） exhibit significant rotational excitation. Furthermore the rotational excitation of CO at the v＂=0 level is noticeably higher than that at the v＂=1 level. （ii） It was found that the major photodissociation pathway of ketene at 218 nm is the CH2（ǎ^1A1）＋CO（X^1∑^＋） channel, while the CH2（b^1B1）＋CO（X^1∑^＋） channel and the CH2（X^3B1）＋CO（X^1E^＋） channel are also likely present, （iii） The anisotropy parameters β of CO different rovibronic states all appear to be larger than zero. No significant difference is observed at the two vibrational states,

Effects of Phosphate Adsorption on Adsorption-Desorption and Availability of Cu and Zn Ions in Ultisols and Alfisols

Surface charge, secondary adsorption- desorption and form distribution of Cu2+ and Zn2+ in Ultisols and Alfisols having adsorbed phosphate were studied by potentiometric titration, adsorption equilibrium and sequential extraction method, respectively. The soil surface negative charges increased whereas the amount of positive charges decreased with increase of P adsorbed. The soil secondary adsorption capacity for Cu2+ and Zn2+ was positively significantly correlated with the amount of P adsorbed by the soils, which could be described by the Langmuir equation. The amounts of Cu2+ and Zn2+ desorption from soils were decreased after P adsorption by the soils and the relationship between them was linear. After the soils adsorbed P, form distribution of Cu2+ and Zn2+ in soils changed remarforbly.

Hydrolysis of Aluminum Ions in Kaolinite and Oxisol Suspensions as Influenced by Organic Anions

To evaluate the role of kaolinite and variable charge soils on the hydrolytic reaction of Al, the hydrolysis of Al ions in suspensions of a kaolinite and an Oxisol influenced by organic anions was investigated using changes of pH, Al adsorption, and desorption of pre-adsorbed Al. Kaolinite and the Oxisol promoted the hydrolytic reaction of Al above a certain initial Al concentration (0.1 mmol L-1 for kaolinite and 0.3 mmol L-1 for the Oxisol). The Al hydrolysis accelerated by kaolinite and the Oxisol increased with an increase in initial concentration of Al and was observed in the range of pH from 3.7 to 4.7 for kaolinite and 3.9 to 4.9 for the Oxisol. The acceleration of Al hydrolysis also increased with the increase of solution pH, reached a maximum value at pH 4.5, and then decreased sharply. Al hydrolysis was promoted mainly through selective adsorption for hydroxy-Al. Soil free iron oxides compensated a portion of the soil negative charge or masked some soil surface negative sites leading to a decrease in Al adsorption, which retarded acceleration to some extent. For the Oxisol organic anions increased the proportion of adsorbed Al3+ in total adsorbed Al with the increase in soil negative surface charge and eliminated or reduced the acceleration of Al hydrolysis. Different organic anions inhibited the hydrolysis of Al in the order: citrate > oxalate > acetate (under initial pH of 4.5). The formation of Al-organic complexes in solution also inhibited the hydrolysis of Al.

Effects of Organic Anions on Phosphate Adsorption and Desorption from Variable-Charge Clay Minerals and Soil

Effects of citrate and tartrate on phosphate adsorption and desorption from kaolinite, goethite, amorphous Al-oxide and Ultisol were studied. P adsorption was significantly decreased as the concentration of the organic anions increased from 10-5 to 10-1 M. At 0.1 M and pH 7.0, tartrate decreased P adsorption by 27.6% - 50.6% and citrate by 37.9 - 80.4%, depending on the kinds of adsorbent. Little Al and/ or Fe were detected in the equilibrium solutions, even at the highest concentration of the organic anions. Effects of the organic anions on phosphate adsorption follow essentially the competitive adsorption mechanism.The selectivity coefficients for competitive adsorption can be used to compare the effectiveness of different organic anions in reducing P adsorption under given conditions.Phosphate desorption was increased by 3 to 100 times in the presence of 0.001 M citrate or tartrate compared to that in 0.02 M KC1 solution alone. However, for all the soil and clay minerals studied the amount of P desorbed by citrate or tartrate was generally lower than or close to that of isotopically exchangeable P. The effect of organic anions on phosphate desorption arises primarily from ligand exchange.

Sonolytic degradation of 2-chlorobiphenyl

The sonolytic degradation of 2-chlorobiphenyl was investigated. Mass spectroscopy was used to detect the products of sonolytic degradation of 2-chlorobiphenyl. The results show that the products of sonolytic degradation, such as biphenyl, ethyl benzene, diethylbiphenyl, dibutylbiphenyl, phenol, propylphenol and di-tert-butyl phenol are produced by thermolysis and hydroxyl free radical reactions, in which biphenyl counts for almost 40%（mole fraction） of the mother compound and others are at trace level. Rapid accumulation of chloride ion shows quick dechlorination, and 78% organic chlorine is converted into chloride ion. Free radical scavengers, bicarbonate and carbonate, decrease the reaction rate of sonolytic degradation of 2-chlorobiphenyl significantly, and the pseudo 1st order rate constant of sonolytic degradation of 2-chlorobiphenyl decreases linearly with the natural logarithm of the concentration of the added free radical scavenger, showing that the pyrolysis and hydroxyl free radical reaction are the two major pathways for the sonolytic degradation of 2-chlorobiphenyl, in which the hydroxyl radical concentration is estimated to be 1×10-10 （mol/L.）

First-principles Study of Adsorption and Dissociation of Methanol on the Pt（lO0） Surface

Using first-principles calculations, we studied the interaction of methanol with the Pt（100） surface based on generalized gradient approximation. We found that top sites of Pt（100） surface are the favored adsorptive positions in energy, and methanol molecule interacts with the Pt surface through oxygen atoms. Moreover, we also explored the possible dissociation pathways of methanol on the Pt surface, and suggested that the products of dissociation can be controlled by the external manipulation.

New Periodic Wave Solutions and Their Interaction for （2＋1）-dimensional KdV Equation

A class of new doubly periodic wave solutions for （2＋1）-dimensional KdV equation are obtained by introducing appropriate Jacobi elliptic functions and Weierstrass elliptic functions in the general solution（contains two arbitrary functions） got by means of multilinear variable separation approach for （2＋1）-dimensional KdV equation. Limiting cases are considered and some localized excitations are derived, such as dromion, multidromions, dromion-antidromion, multidromions-antidromions, and so on. Some solutions of the dromion-antidromion and multidromions-antidromions are periodic in one direction but localized in the other direction. The interaction properties of these solutions, which are numerically studied, reveal that some of them are nonelastic and some are completely elastic. Furthermore, these results are visualized.

Adsorption Mechanism of Water Molecule on Goethite(010) Surface

Abstract Goethite widely exists among ocean sediments; it plays an important role in fixing heavy metals and adsorbing organic contaminants. So the understanding of the adsorbing process of water molecule on its surface will be very helpful to further reveal such environmental friendly processes. The configuration, electronic properties and interaction energy of water molecules adsorbed on pnma goethite （010） surface were investigated in detail by using density functional theory on 6-31G （d,p） basis set and projec- tor-augment wave （PAW） method. The mechanism of the interaction between goethite surface and H20 was proposed. Despite the differences in total energy, there are four possible types of water molecule adsorption configurations on goethite （010） surface （Aa, Ab, Ba, Bb）, forming coordination bond with surface Fe atom. Results of theoretical modeling indicate that the dissociation process of adsorbed water is an endothermic reaction with high activation energy. The dissociation of adsorbed water molecule is a proton transportation process between water＇s O atoms and surface. PDOS results indicate that the bonding between 1-120 and （010） surface is due to the overlapping of water＇s 2p orbitals and Fe＇s 3d orbitals. These results clarify the mechanism on how adsorbed water is dissociated on the surface of goethite and potentially provide useful information of the surface chemistry of goethite.

Polymer donor with halogenated-aromatic side chain enables efficient ternary organic solar cells

Ternary strategy has demonstrated great potential in promoting the power conversion efficiency(PCE)of bulk heterojunction organic solar cells(BHJ OSCs).Two new polymer donors,TPQ-2 F-2 Cl and TPQ-2 F-4 F,were synthesized with chlorinated and fluorinated aromatic side chains,respectively,which contributed to distinct noncovalent interactions.Compared with the PM 6:L 8-BO host system,the TPQ-2 F-2 Cl based ternary OSCs obtained enhanced exciton dissociation and more balanced carrier mobility.Moreover,benefiting from the favorable miscibility of the PM 6:L 8-BO:TPQ-2 F-2 Cl blend,the ternary blending film featured a well-defined fibrillar morphology and improved molecular ordering.Consequently,the optimal PM 6:L 8-BO:TPQ-2 F-2 Cl device achieved a more outstanding PCE of 18.2%,a higher open circuit voltage(V_(oc)),and a better fill factor(FF)in comparison with the binary device(PCE=17.7%).In contrast,the addition of TPQ-2 F-4 F would generate excessive aggregation of blend,thereby reducing the PCE of ternary OSCs(16.0%).This work shows a promising idea for designing efficient third component donor polymers.

Isolation and Identification of Phosphobacteria in PoplarRhizosphere from Different Regions of China

A few soil microorganisms can convert insoluble forms of phosphorus （P） to an accessible form to increase plant yields The objectives of this study were to isolate, screen and identify the phosphobacteria, i.e., phosphate-solubilizing bacteria （PSB） and phosphate-mineralizing bacteria （PMB）, in some poplar plantations and to select potential microbial inoculants that could increase the P uptake by plants. Seventy four PSB strains and 138 PMB strains were preliminarily screened from 797＂colonies isolated from the rhizosphere soil of poplar by the visible decolorization in the National Botanical Research Institute＇s phosphate growth medium （NBRIP） containing a pH indicator of bromophenol and by the clear/halo zone on yeast malt agar plate, respectively. Then, based on the solubilization of Ca3（PO4）2 in liquid NBRIP medium and the mineralization of lecithin in liquid Menkina medium, 15 PS1R strains and 7 PMB strains were further determined for their abilities to solubilize Ca3（PO4）2 and to mineralize lecithin. The results showed that the 15 PSB strains exhibited inorganic P-solubilizing abilities ranging between 376.62 and 669.56 mg L-1 and the 7 PMB strains exhibited organic P-mineralizing abilities vaxying from 0.32 to 1.56 mg L-1 three days after incubation. Three of PSB strains with the highest P-solubilizing ability, named JW-JS1, JW-JS2 and JW-SX2, were all preliminarily identified as Pseudomonas ftuorescens, while two of PMB strains with the highest P-mineralizing ability, named JYZ-SD1 and JYT-JS2, were preliminarily identified as Bacillus cereus and Bacillus subtilis, respectively. All the efficient PSB and PMB strains should be further studied under both pot culture and field conditions to test their beneficial effects on poplar.

Proteomic analysis of primary colon cancer-associated fibroblasts using the SELDI-ProteinChip platform

Objective： Cancer-associated fibroblasts （CAFs） are one of the hallmarks of the cancer microenvironment. Recent evidence has indicated that CAFs are more competent in enhancing cancer cell growth and migration than normal fibroblasts. However, the unique protein expression of CAFs has not been fully elucidated. This study aims to investigate the characterizations of colon CAFs by comparing the differential protein expression between CAFs and normal fibroblasts. Methods： Primary fibroblasts were isolated from surgical specimen of human colon cancer and matched normal colonic tissue. Purity of the cell population was verified through immunostain analysis. Total cell lysates and conditioned media from each group of cells were extracted, and protein expression analysis was con- ducted using the surface-enhanced laser desorption/ionization time-of-flight mass spectrometry （SELDI-TOF-MS） ProteinChip platform. Results： Most primary cells showed typical fibroblast-like features after two weeks. Increased proportion of a-smooth muscle actin-positive myofibroblasts was detected within the CAFs in four of the six pairs of primary cells. Fibroblast activation protein was weakly expressed in most cells without differences. Using SELDI-TOF-MS ProteinChip platform, four protein peaks mass over charge ratio （m/z） 1142, 3011, 4035, and 4945 were detected in the total cell lysates, and two protein peaks m/z 1368 and 1389 were detected in the conditioned media. The potential candidate proteins found in the Swiss-Prot database include morphogenetic neuropeptides, FMRFamide-related peptides, insulin-like growth factor II, thymosin 13-4-like protein 3, and tight junction-associated protein 1. Conclusions： Using the SELDI-ProteinChip platform, differential protein expressions were identified in colon CAFs compared with normal colonic stromal fibroblasts. The complex proteomic alternations in colon CAFs may play important roles related to the colon cancer microenvironment.