气相色谱法在粗苯检验中的应用

用气相色谱法对粗苯进行检验，较蒸馏法具有快速、准确、无污染的优点。

芳烃抽提装置技术改造

由于中国石化锦西石化分公司600kt/a连续重整装置的建设,芳烃抽提装置的原料由原来的脱戊烷油变为C_6组分。为此,对抽余油水洗塔和芳烃分离部分的苯塔塔盘,以及苯塔塔顶和塔底抽出部分进行了改造,更换部分机泵和增加变频泵,并将常规仪表改为DCS控制。改造后装置实现一次开车成功,生产出合格产品。抽余油中总芳烃含量小于0.1％,苯回收率达到99％以上。

Proteome profiling of spinal cord and dorsal root ganglia in rats with trinitrobenzene sulfonic acid-induced colitis

AIM: To investigate proteomic changes in spinal cord and dorsal root ganglia (DRG) of rats with trinitrobenzene sulfonic acid (TNBS)-induced colitis. METHODS: The colonic myeloperoxidase (MPO) activity and tumor necrosis factor-(TNF- ) level were determined. A two-dimensional electrophoresis (2-DE)-based proteomic technique was used to profile the global protein expression changes in the DRG and spinal cord of the rats with acute colitis induced by intracolonic injection of TNBS. RESULTS: TNBS group showed significantly elevated colonic MPO activity and increased TNF-level. The proteins derived from lumbosacral enlargement of the spinal cord and DRG were resolved by 2-DE; and 26 and 19 proteins that displayed significantly different expression levels in the DRG and spinal cord were identified respectively. Altered proteins were found to be involved in a number of biological functions, such as inflammation/immunity, cell signaling, redox regulation, sulfate transport and cellular metabolism. The over-expression of the protein similar to potassium channel tetramerisation domain containing protein 12 (Kctd 12) and low expression of proteasome subunit type-1 (psma) were validated by Western blotting analysis. CONCLUSION: TNBS-induced colitis has a profound impact on protein profiling in the nervous system. This result helps understand the neurological pathogenesis of inflammatory bowel disease.

Chromatographic separation of Be（Ⅱ） from Mg（Ⅱ）, Ca（Ⅱ）, Sr（Ⅱ） and Ba（Ⅱ） using poly[dibenzo-18-crown-6] and L-arginine

A simple and selective method for the separation of Be（Ⅱ） was developed using poly[dibenzo-18-crown-6] as a stationary phase in column chromatography. The study was carried out in L-arginine medium. 1.0-8.0 M HCl and CH3COOH, 0.5-8.0 M HBr, HClO4 and H2SO4, 0.2-1.0 M EDTA and 0.02-0.12 M ammonium oxalate were found to be an efficient eluents for Be（Ⅱ）. The capacity of polymer was 0.554-0.01 mmol/g of crown polymer. The tolerance limit of various cations and anions were reported. Be（Ⅱ） was quantitatively separated from Mg（Ⅱ）, Ca（Ⅱ）, Sr（Ⅱ） and Ba（Ⅱ）. The selective separation of Be（Ⅱ） was possible from multicomponent mixtures. The method was extended to determine Be（Ⅱ） from geological samples. Method was simple, rapid and selective having good reproducibility （approximately4-2%）.

Synthesis of Oligohydroxynapthylenes and Their Use in Making of Heat-Stable and Electro-Conducting Rubbers

By oxidative polycondensation of 1-naphthol and their copolycondensation with aniline or p-phenylenediamine the polyfucntional polyconjugated oligomers consisting of hydroxynaphthylene links have been prepared. These soluble and meltable oligomers showing thermostability, semiconducting and paramagnetic properties and also high reactivity at reactions characteristic for aromatic hydroxyl groups were used as active filler at preparation of rubbers from butyl and butadiene-nitrile rubbers. It has been shown that in partial or full substitution of carbon black by oligohydroxynaphthylenes or cooligohydroxynaphthylenephenylamines in composition of vulcanizate the prepared rubbers are characterized by noticeably high heat-physical, physical-mechanical and electrical properties （Pv = 10^8 - 10^6Om. cm ）.

Phenol Composition and Susceptibility to Fusarium oxysporum Dianthi in Carnation

Phenol composition of two carnation （Dianthus caryophyllus） cvs ＂Gloriana＂ and ＂Roland＂, partially and highly resistant to F. oxysporum f. sp. dianthi, respectively, has been investigated with the aim of assessing the possible role of phenolic constituents both as biochemical markers of resistance and antifungal molecules. Analyses were performed through chromatography, NMR and MS methods. The results indicate that protocatechuic and vanillic acids are present in healthy and infected tissues of both cvs; the flavonol glycoside peltatoside. 2,6-Dimethoxybenzoic acid was detected in small amounts only in infected ＂Gloriana＂ cv while the highly resistant ＂Roland＂ cv contained the flavone datiscetin. This latter compound, due to its noticeable antifungal activity evidenced in in vitro trials, could be conceived both as a biochemical marker of resistance towards this pathogen and as a phytoanticipin.

One-pot three-component synthesis of tetrahydrobenzo[b]pyrans catalyzed by cost-effective ionic liquid in aqueous medium

A simple and ef ficient method is proposed for the synthesis of tetrahydrobenzo[b]pyrans with aromatic aldehydes, active methylene compounds, and dimedone using basic ionic liquid catalyst in water. The procedure offers several advantages including short reaction time, good yield, easy procedure, and good recyclability of catalysts, which may be a practical alternative to conventional processes for preparation of 4-hpyrans.

Template-directed assembly of pentacene molecules on epitaxial graphene on Ru（0001）

The template-directed assembly of planar pentacene molecules on epitaxial graphene grown on Ru（0001） （G/Ru） has been investigated by means of low-temperature scanning tunneling microscopy （STM） and density functional theory （DFT） calculations. STM experiments find that pentacene adopts a highly selective and dispersed growth mode in the initial stage. By using DFT calculations including van der Waals interactions, we find that the configuration with pentacene adsorbed on face-centered cubic （fcc） regions of G/Ru is the most stable one, which accounts for the selective adsorption at low coverage. Moreover, at high coverage, we have successfully controlled the molecular assembly from amorphous, local ordering, to long-range order by optimizing the deposition rate and substrate temperature.

Polystyrene-based blend nanorods with gradient composition distribution

The polystyrene-based polymer blends, partially miscible poly(bisphenol A carbonate)/polystyrene (PC/PS) and completely miscible poly(2,6-dimethylphenylene oxide)/polystyrene (PPO/PS), in nanorods with gradient composition distribution were discussed. The polymer blend nanorods were prepared by infiltrating the polymer blends into nanopores of anodic aluminum oxide (AAO) templates via capillary action. Their morphology was investigated by micro-Fourier transform infrared spectroscopy (micro-FTIR) and nano-thermal analysis (nano-TA) with spatial resolution. The composition gradient of polymer blends in the nanopores is governed by the difference of viscosity and miscibility between the two polymers in the blends and the pore diameter. The capillary wetting of porous AAO templates by polymer blends offers a unique method to fabricate functional nanostructured materials with gradient composition distribution for the potential application to nanodevices.

Multi-component hydrogen-bonding salts formed between imidazole and aromatic acids:Synthons cooperation and crystal structures

Imidazole base was crystallized with different aromatic carboxylic acids 2,4-dihydroxybenzoic acid, 5-chlorosalicylic acid, and 1,8-naphthalic acid, affording three new binary molecular organic salts of [(C 3 H 5 N 2 + )·(C 7 H 5 O 4 )] (1), [(C 3 H 5 N 2 + )·(C 7 H 4 O 3 Cl )] C 7 H 5 O 3 Cl (2), and [(C 3 H 5 N 2 + ) (C 12 H 7 O 4 )] (3). Proton transfer occurs from the COOH of carboxylic acid to nitrogen of imidazole in all complexes (1-3), leading to the hydrogen bond N-H…O in all structures. To our knowledge, the recognition pattern between the carboxylic acid group and imidazole (acid-imidazole synthon) is less well-studied so far. The cooperation among COOH, COO and imidazolium cation functional groups for the observed hydrogen bond synthons is examined in the three structures. Generally, the strong N-H…O and O-H…O hydrogen bonds define supramolecular architecture and connectivity within chains, while weaker C-H…O hydrogen bonds play the dominant role in controlling the interactions between layers in these novel organic salts. Thermal stability of these compounds has been investigated by thermogravimetric analysis (TGA) of mass loss.

Intermolecular dearomative oxidative coupling of indoles with ketones and sulfonylhydrazines catalyzed by I2:synthesis of[2,3]-fused indoline tetrahydropyridazines

A convergent construction of [2,3]-fused indoline tetrahydropyridazines via an I2/tert-butyl hydroperoxide(TBHP) catalyzed three-component dearomative oxidative coupling of indoles, hydrazines and acetophenone was established in moderate to good yields. This protocol provides a new approach for the synthesis of these biologically interesting fused indolines.

Correlation between the molecular structure and transcis isomerization characteristics of azobenzenes

Photochemical and thermal isomerization of various azobenzenes was systematically investigated to understand the correlation between the molecular structure and trans → cis isomerization characteristics of azobenzenes. A blue shift in π-π absorption band of ortho-alkylated azobenzenes （1o and 2o） was observed together with a reduction in molar extinction coefficient （e） in comparison with both meta-alkylated azobenzenes （4m and 5m） and 7p lacking the meta and ortho substituents. For orthoalkylated azobenzene, photochemical trans-to-cis isomerization and thermal back cis-to-trans isomerization in solution oc- curred slowly when compared with 4m, 5m and 7p. The half-life time of the cis form of 20 was found to be 380 h, which is about 8-50 times longer than those of comparable 4m, 5m （43-13 h） and 7p （7 h）. Furthermore, comparison of the molecular structure and isomerization characteristics of azobenzene thiol （20 and 5m） self-assembled monolayers on flat gold surfaces indicates that the trans-to-cis photoconversion in monolayer systems is influenced by steric hindrance and strong intermoleculax interaction between azobenzene units.

Ternary Fe3O4@PANI@Au nanocomposites as a magnetic catalyst for degradation of organic dyes

Magnetic Fe_3O_4@PANI@Au nanocomposites are fabricated through electrostatic self-assembly and seed growth methods.The rate constant K_(app) is calculated to be 8.63×10^(-3) s^(-1) at room temperature for the reduction of 4-nitrophenol to 4-aminophenol with an excessive amount of NaBH_4 as a model system showing outstanding catalytic efficiency and stability.For recyclable performance,the catalyst exhibits slight loss in catalytic performance on the conversion of 4-nitrophenol after running for more than 10 cycles.Besides,the smaller and simpler the structure,the easier the molecular structure can be degraded,and the faster the cationic dyes can be degraded than the anionic dyes,which can reveal the selectivity.For practical application,Congo red as a pollutant of the lake water is degraded rapidly after Fe_3O_4@PANI@Au is added to the solution in a few minutes.It has been demonstrated that magnetic Fe_3O_4@PANI@Au nanoparticle composite is a promising catalyst for environment sewage.