CFB煤燃烧/热解双反应器中热解室对立管内气固流动特性的影响

考察了循环流化床煤燃烧/热解双反应器系统中热解室的存在对立管内的压力分布及气固流动状况的影响。提升管的内径100 mm、高6 m，立管的内径44 mm、高3 m，热解室的截面积200 mm×200 mm、高770 mm。结果表明，随着提升管内表观气速Ur的增加，有无热解室立管内均为负压差流动，负压差梯度随着Ur的增加而减小。有热解室时，热解室内要保持一定的料位高度，整个立管内固体颗粒的流动为负压差移动床流动；没有热解室时，立管内为稀相流动和移动床流动同时存在，立管内平衡料柱高度随Ur的增加而升高。随着循环量Gs的增加，两种类型的立管内负压差梯度均随之增大，也存在着流动形态的差别。循环量Gs的增加会引起立管内平衡料柱高度的降低。立管内气固相对滑移速度也随着循环量Gs的增加而增大。     

菲林B近红外分光光度法测定维生素C

在pH 3的三氯乙酸酸性介质中,菲林B可以定量地将还原型维生素C氧化成脱氢型维生素C,利用脱氢型维生素C在920 nm处有最大吸光度,测定其含量,建立了一种测定维生素C的新方法,并研究了影响反应的各种因素。该方法对维生素C的检出限为0.17 mg/L;线性范围为0.5~10 mg/L,对水果中维生素C含量测定的RSD<2.31%;回收率为99.7%~101.1%,比2,4-二硝基苯肼分光光度法测定结果的相对偏差<±1.6%。     

In vitro TRANSFORMATION OF RAT ESOPHAGEAL EPITHELIAL CELLS BY FUSARIN C

Fusarin C (FC) is a mutagenic and carcinogenic mycotoxin which was isolated from Fu-sarium moniliforme culture extracts. The Fusarium moniliforme is one of most prevalent fungi found on corn in Linxian, a high risk area for esophageal cancer. This paper reports, for the first time, the malignant transformation of rat esophageal epithelial cells induced by FC. The transformed cells showed several characteristics of transformation. Colonies were formed after seeding these transformed cells either into selective medium free of epidermal growth factor (EGF) and serum, or on semi-solid agar; there was an increase in chromosome number; the expression of c-myc and v-erb-B oncogenes was enhanced in the cells; and squamous cell carcinomas arose after inoculating the cells into nude mice. The results demonstrated transforming effect of FC on rat esophageal epithelial cells, and indicate that the abnormal expression of some oncogenes could serve as a hew property of transformed cells.     

Fluordiazadiphosphetidine, 11. Mitt.: Eine neue Methode zur Herstellung der doppelt zwitterionischen Verbindung (CH3N)6P4F8

A new synthetic route for the preparation of the betain-like compound (CH₃N)₆P₄F₈ from (CH₃NPF₃)₂,N-methyl-hexamethyldisilazane andN,N-dimethyl-urea has been found. The steps of this multi-stage reaction could be rationalized to a far extent.

10. Mitteilung:Kubjacek M., Utvary K., Mh. Chem.112, 305 (1981).     

A theoretical study on a fullerene derivative C54N4 and some of its protonated forms

Semiempirical quantum chemical calculations at the level of AM1 (restricted Hartree–Fock) have been performed on a fullerene derivative, C₅₄N₄, theoretically obtained from C₆₀ and its mono and diprotonated forms. All these structures are stable, but endothermic in nature. Some calculated geometrical and physicochemical properties of these have also been reported.     

Chromatographic separation and mass spectrometric identification of positional isomers of polyethylene glycol-modified growth hormone-releasing factor (1-29)

A one-step chromatographic method capable of separating all isomers of polyethylene glycol (PEG)-growth hormone-releasing factor (GRF) (1-29) conjugates was developed. The unmodified GRF (1-29) and seven different isomers of PEG-GRF (1-29) conjugates were separated by using a simple reversed-phase HPLC method depending on the differences of hydrophobicity due to the number and site of PEG attachment. The PEGylation sites of all isomers of PEG-GRF (1-29) conjugates were identified by determining the molecular masses of the Lys-C digested fragments with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. This study is a first report for the separation of all PEG-conjugate isomers and would be useful for further studies to find the promising conjugate by evaluating biological activity and stability of each isomer.     

Comparison between self-reinforced composites based on ultra-high molecular weight polyethylene fibers and isotropic UHMWPE

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固体超强酸催化剂SO_4~(2-)/TiO_2-WO_3的制备及其催化性能研究

制备了固体超强酸催化剂SO2 -4/TiO2 WO3 ,并以丁酸丁酯的合成作为探针反应 ,系统考察了WO3 的含量、硫酸浸渍浓度、焙烧温度等制备条件对SO2 -4/TiO2 WO3 催化活性的影响 .实验表明 :制备催化剂的适宜条件为m(H2 WO4) =12 5 % ,硫酸浸渍浓度为 1 0mol·L-1,焙烧温度为 5 80℃ ,活化时间 3h .利用优化条件下制备的催化剂SO2 -4/TiO2 WO3 催化合成缩醛 (酮 ) ,在醛 /酮与二元醇 (乙二醇 ,1,2 丙二醇 )的投料摩尔比为 1∶1 5 ,催化剂的用量占反应物总投料质量的 0 5 % ,反应时间为 1h条件下 ,2 甲基 2 乙氧羰甲基 1,3 二氧环戊烷的收率为 78 7% ,2 ,4 二甲基 2 乙氧羰甲基 1,3 二氧环戊烷的收率为 83 0 % ,环己酮 -乙二醇缩酮的收率为 85 9% ,环己酮 1,2 丙二醇缩酮的收率为 84 6% ,丁酮 -乙二醇缩酮的收率为70 7% ,丁酮 1,2 丙二醇缩酮的收率为 88 3 % ,2 丙基 1,3 二氧环戊烷的收率为 80 6% ,4 甲基 2 丙基 1,3 二氧环戊烷的收率为 79 6% ,2 异丙基 1,3 二氧环戊烷的收率为 64 2 % ,4 甲基 2 异丙基 1,3 二氧环戊烷的收率为 83 3 % ,2 苯基 1,3 二氧环戊烷的收率为 75 3 % ,4 甲基 2 苯基 1,3 二氧环戊烷的收率为 95 1% .     

Tautomerism and Acidic Properties of N‐Unsubstituted Benzohydroxamic Acids: Semiempirical Quantum Chemical Estimation

Tautomerism of Nunsubstituted benzohydroxamic acids and their anions in the gas phase was investigated by the semiempirical AM1 method. The possibility of estimating pK _a in aqueous solutions using calculated characteristics of molecules is demonstrated.     

New unsymmetrical difluoroaromatic compounds and estimation of their reactivities in nucleophilic substitution

A series of previously unknown unsymmetrical difluoroaromatic compounds, viz., p-fluorobenzoylphenyl(p-fluorophenyl)-substituted imidazoles, pyrazines, and quinoxalines, were synthesized according to multistep procedures with the use of chloral as the key compound. The reactivities of the resulting difluoroaromatic compounds were estimated based on ¹⁹F and ¹³C NMR spectral data and the results of quantum-chemical calculations. The calculated charge densities on the C_ipso atoms correlate linearly with the experimental chemical shifts in the ¹⁹F and ¹³C NMR spectra. Difluoroaromatic compounds, which are characterized by _F > –110 and _C > 163 and by the charge density on the C_ipso atom higher than 0.08 e, are sufficiently activated to be used for the preparation of high-molecular-weight polyethers.