八烷基氮杂对环仿三氟甲基磺酸盐的合成

从四氮杂对环仿（ｔｅｔｒａａｚａｐａｒａｃｙｃｌｏｐｈａｎｅ）合成得到四烷基氮杂对环仿，再以三氟甲基磺酸甲酯作甲基化试剂，合成得到２种未见文献报道的八烷基氮杂对环仿三氟甲基磺酸盐，提供了新的人工模拟酶有机化合物。

A novel surfactant N-hydroxy-9,10-epoxy group-octadecanamide:Part II.Its synthesis and application in flotation separation of spodumene and albite

A novel hydroxamic acid,N-hydroxy-9,10-epoxy group-octadecanamide(N-OH-9,10-O-ODA),was synthesised by modifying the structure of oleic acid.The carboxyl group of oleic acid was converted into an N-hydroxy amide group,and an epoxy group was introduced into its structure.N-OH-9,10-O-ODA was used as a novel collector in the flotation separation of spodumene from one of its associated gangue minerals,specifically albite.N-OH-9,10-O-ODA exhibits remarkable selectivity,with a stronger affinity for collecting spodumene particles compared to albite particles.Zeta potential measurements and X-ray photoelectron spectroscopic analysis reveal that the adsorption quantity of N-OH-9,10-O-ODA on spodumene surface is comparable to that on albite surface.First-principles calculations demonstrate the diverse adsorption configurations of N-OH-9,10-O-ODA on surfaces of spodumene and albite,leading to its distinct collecting abilities for spodumene and albite particles.

溶胶凝胶法制备混合硅烷毛细管整体柱

以八烷基三乙氧基硅烷和甲基丙烯酰氧丙基三甲氧基硅烷为混合单体,利用溶胶-凝胶及光聚合法快速制备了毛细管电色谱整体柱,研究了不同配比的单体对中性物质保留行为的影响.分别采用电色谱、加压电色谱和低压色谱模式对所制备的整体柱进行了色谱性能评价.七种模型物质均能得到基线分离,整体柱均体现反向色谱的分配机理.对硫脲的最大理论塔板数可达20 000/m以上.扫描电镜结果表明所形成整体材料具有致密的网络结构且与管壁结合紧密.

Metabolites of Marine-derived Mangrove Endophytic Fungus #2492 from the South China Sea

Two metabolites （A and B） were isolated from the mycelium of mangrove endophytic fungus Stysanus like sp. （#2492） from the South China Sea. Their structures were identified by spectral data as N-（2-hydroxytetracosyl）-2-amino-1,3,4-trihydroxyoctadecane （A） and γ -stearolactone （B）. It is the first report that γ -stearolactone （B） is isolated from marine fungus as natural product.

[bmim]Cl/[FeCl3] Ionic Liquid as Catalyst for Alkylation of Benzene with 1-Octadecene

Abstract The study on the catalysis of ionic liquids for alkylation of benzene with 1-octadecene to synthesize LAB （linear alkylbenzenes） was performed. The results showed that the most important factor that governed the conversion of olefin and selectivity of LAB was reaction temperature. Moreover, the effects of different ionic liquids and molar ratio of benzene to 1-octadecene on the conversion and selectivity were obviously in different degrees. The reaction temperature, molar ratio of benzene to 1-octadecene and the amount of catalyst were lower, compared with the traditional reaction technologies. The experimental results demonstrated that the ionic liquid had higher activity at 30℃, with over 98% selectivity of monoalkylbenzene and 100% conversion of the olefin at the molar ratio 0.08 of FeCl3 in ionic liquid to 1-octadecene and 10 for benzene to 1-octadecene.

Cationic Ring Opening Polymerization of Octamethylcyclotetrasiloxane Initiated by Acid Treated Bentonite

Cationic ring opening polymerization of octamethylcyclotetrasiloxane （Da） initiated by acid treated bentonite was investigated. The experimental conditions were chosen on the basis of preliminary experiments.Higher temperature was found beneficial for the reaction process while stirring intensity beyond a certain level showed no obvious effect on the reaction rate. Polymers were characterized by Fourier transform infrared, proton nuclear magnetic resonance （IH-NMR） and gel perneation chromotography. The width of molecular mass distribution was found ranging between 1.2 and 1.4, which is extraordinarlly narrow compared with that of cationic polymerizations reported elsewhere （〉 1.9）. The results were believed due to the absence of free proton and counter ion which simplifies the polymerization process and the huge steric hindrance provided by bentonite particles which keeps the propagation of polysiloxane onto the surface of bentonite particles in a much more regular way. A feasible mechanism is proposed and seems to be supported well by experiments. Additionally, from the results of α, ω-dihydrogen terminated polysiloxanes prepared, the possibility of applying this potential environmentally friendly heterogeneous catalyst in industrial polymerization of cyclosiloxanes is anticipated.

Variation of Surface Adhesion Force During the Formation of OTS Self-assembled Monolayer Investigated by AFM

Variation of the surface adhesion force during the formation of octadecyl trichlorosilane (OTS) self-assembled monolayer on a glass substrate surface was investigated by atomic force microscope (AFM). The research shows that the hydrophobicity and the adhesion force of the sample surface increases gradually while the substrate surface is covered by OTS molecules as the reaction proceeds. After 15min reaction, a close-packed and smooth OTS self-assembled monolayer could form on the glass substrate surface with an advancing contact angle of 105° and an interfacial energy of 55.79mJ·m-2.

Chemical Modification and Characterization of Multi-Walled Carbon Nanotubes Using Octadecylamine and Polyethylene Glycol

Chemical modification of MWCNTs via oxidation followed by side wall functionalization using polyethylene glycol （PEG） and octadecylamine （ODA）, separately, was studied. Different characterization techniques such as FTIR spectrometery, thermogravimetric analysis （TGA）, scanning electron microscopy （SEM）, X-ray diffraction （XRD）, and solubility in different solvents were performed for the oxidized MWCNTs, MWCNTs-PEG and MWCNTs-ODA. The characterization techniques proved the presence of the functional groups on the MWCNTs surface. Thermal gravimetric analysis revealed that nearly 16% （by weight） of the MWCNTs were functionalized with PEG and 39% （by weight） was functionalized with ODA.

Study on the Effect of Surface Modification on the Properties of Bentonite Greases

In order to investigate the influening factors of organic modification procedure and find out connections between organic modification and the properties of bentonite greases, organic montmorillonite(OMMT) thickeners with different surfactant dosages and constituents were synthesized through intercalation reaction between sodium montmorillonite(NaM MT) and quaternary ammonium surfactants in aqueous solvents. The lubricating greases were prepared with the resulting organoclays, while the penetration and oil separation of lubricating greases were evaluated, respectively. The surface modification process of montmorillonite(MMT) was analyzed and the thickening mechanism of OMMT was discussed in this study. The experimental results showed that, with an increasing amount of surfactant, the basal spacing between the clay platelets was increasing and the structure of modifier molecules layer in the interlayer was changing from lateral bilayer to paraffin-type bilayer. The optimal properties of lubricating greases were achieved, when the structure of surfactant molecules loaded in the interlayer was the paraffin-type monolayer, which meant that the dosage of modifier was equal to 120—140 mmol/(100g). Meanwhile, it was found that the thickening performance, colloid stability, anti-wear and friction-reducing performance of lubricating greases were improved, when the surfactants were mixed with octadecyl trimethyl ammonium chloride(OTAC) and hexadecyl trimethyl ammonium chloride(HTAC). And the optimum mole ratio of two surfactants is was 1:1.

Kinetics of Bulk Polymerization of Octamethylcyclote- trasiloxane

The kinetics of bulk polymerization of octamethylcyclotetrasiloxane under acid circumstance is studied. A kinetic model is put forward and kinetic parameters are obtained through optimization.