三种特殊的双固定步网络环的生成树的数目

令Ｔ（Ｃ＾－（ｎ，ｌ，ｐ）是双固定步网络环Ｃ＾－（ｎ，ｌ，ｐ）的生成树的数目，在本文中给出了关于Ｔ（Ｃ＾－（ｎ，１，２）），Ｔ（Ｃ＾－（ｎ，１，３）和Ｔ（Ｃ＾－（ｎ，１，４））的三种递推式，且一般情况，Ｔ（Ｃ＾－（ｎ，１，ｐ）也可以按此思想考虑。     

Heterogeneous photocatalyzed degradation of a pesticide derivative, 3-chloro-4-methoxyaniline, in aqueous suspensions of titania

The photocatalyzed degradation of a pesticide derivative, 3-chloro-4-methoxyaniline (1), has been investigated in aqueous suspensions of titanium dioxide (TiO₂) and air as a function of irradiation time under a variety of conditions using UV?CVis spectroscopic and HPLC analysis techniques. The degradation kinetics were studied under different conditions such as types of TiO₂ powders, reaction pH, catalyst loading, substrate, and H₂O₂ concentrations. The photocatalyst Degussa P25 showed better photocatalytic activity for the degradation of the compound 1. Addition of hydrogen peroxide as an electron acceptor in addition to oxygen greatly enhanced the degradation rate of the compound 1. Higher degradation rates were observed at lower and higher pH values, i.e., 3.15 and 9.15, respectively. The optimal substrate concentration and catalyst loading for the degradation was found to be 0.6?mM with 1.5?g?L^?1. A probable pathway for the decomposition of compound 1 is proposed.     

Effects of pure AcOH and mixed AcOH–CS (CS?=?CH3CN and THF) solvents on the rate of cleavage of phthalic anhydride (PAn)

The values of pseudo-first-order rate constants (k _obs) for the acetolysis of phthalic anhydride (PAn) increase from 6.60?×?10^?7 to 31.5?×?10^?7?s^?1 with the increase in temperature from 30 to 50?°C. These values of k _obs give activation parameters ?H* and ?S* as 14.4?±?0.4?kcal?mol^?1 and ?39.1?±?1.3?cal?K^?1?mol^?1, respectively. The values of k _obs remain essentially unchanged with the increase in the content of CS (CS?=?CH₃CN or THF) from 0 to 40?% v/v in mixed AcOH?CCS solvents. These observations have been explained qualitatively.     

提高维吾尔文搜索质量的一些关键技术研究

维吾尔语和土耳其语、乌兹别克语、哈萨克语等同属于阿尔泰语系突厥语分支,是一种粘着型语言,具有丰富的构词合构形附加成分.主要分布于中国新疆维吾尔自治区,以及中西亚地区的维吾尔族使用.目前使用基于阿拉伯文字母的维吾尔文.当前用google,bing等搜索引擎搜索维吾尔文时搜索结果不包括该词语的构词合构形附加成分等其它形式.严重影响了搜索结果的准确性.通过词干提取和词缀附加生成词语组合的方法以解决提高维吾尔文搜索质量的问题.此问题解决,将在大幅度提高维吾尔文搜索的准确性,并针对提高其它突厥语族语言(土耳其语、乌兹别克语、哈萨克语等)的搜索质量、数据挖掘、数据分析、数据安全、自然语言理解等研究领域有一定的参考价值.     

Degradation and toxicity reduction of textile wastewater using immobilized titania nanophotocatalysis

The feasibility and performance of photocatalytic degradation and toxicity reduction of textile dye (Acid Blue 25) have been studied at pilot scale in an immobilized titania nanoparticle photocatalytic reactor. UV-Vis, Ion Chromatography (IC) and chemical oxygen demand (COD) analyses were employed to obtain the details of the photocatalytic dye degradation. The effects of operational parameters such as H2O2, pH and dye concentration on the photocatalytic degradation of Acid Blue 25 were investigated. The aliphatic carboxylic acid intermediates and inorganic anions generated during the dye degradation process were analyzed. Daphnia magna bioassay has been used to test the progress of toxicity during the treatment process. Total disappearance of dye was attained. During the photocatalytic treatment process, the residual acute toxicity was reduced. The results showed that immobilized titania nanophotocatalysis capable to degradation and toxicity reduction of acid dye textile wastewater.     

Kinetics and mechanism of intramolecular general base-catalyzed alkanolysis of phenyl salicylate in the presence of anionic micelles

The alkanolysis of ionized phenyl salicylate, PS^?, has been studied in the presence and absence of micelles of sodium dodecyl sulphate, SDS, at 0.05 M NaOH, 30 or 32°C and within the alkanol, ROH, (ROH = HOCH₂CH₂OH and CH₃OH) contents of 15–74 or 92%, v/v. The alkanolysis of PS^? involves intramolecular general base catalysis. At a constant concentration of SDS, [SDS]_T, the observed pseudo first-order rate constants, k_obs, for the reactions of ROH with PS^? obtained at different concentration of ROH, [ROH]_T, obey the relationship: k_obs = k[ROH]_T/(1 + K_A[ROH]_T) where k is the apparent second-order rate constant and K_A is the association constant for dimerization of ROH molecules. Both k and K_A decrease with increase in [SDS]_T. At a constant [ROH]_T, the rate constants, k_obs, show a decrease of nearly 2-fold with increase in [SDS]_T from 0.0–0.3M. These results are explained in terms of pseudo-phase model of micelle. The rate constants for alkanolysis of PS^? in micellar pseudophase are insignificant compared with the corresponding rate constants in aqueous-alkanol pseudophase. This is attributed largely to considerably low value of [ROH] in the specific micellar environment where micellar bound PS^? molecules exist. The increase in [ROH]_T decrease the value of the binding constant of PS^? with SDS micelle. The effects of anionic micelles on the rates of alkanolysis of PS^? are explained in terms of the porous cluster micellar structure.     

Kinetics and mechanism for the formation of o‐carboxy(N‐methyl)‐benzohydroxamic acid in the cleavage of ethyl N‐[o‐(N‐methyl‐N‐hydroxycarbamoyl)‐benzoyl]carbamate in N‐methylhydroxylamine,acetate, and phosphate buffers

The rate of cleavage of ethyl N‐[o‐(N‐methyl‐N‐hydroxycarbamoyl)benzoyl]‐ carbamate (ENMBC) in the buffer solutions containing N‐methylhydroxylamine, acetate + N‐methylhydroxylamine, and phosphate + N‐methylhydroxylamine followed an irreversible consecutive reaction path: ENMBC where A and B represent N‐hydroxyl group cyclized product of ENMBC and o‐(N‐methyl‐N‐hydroxycarbamoyl)benzoic acid, respectively. Both rate constants k_{1 obs} and k_{2 obs} showed the presence of buffer catalysis, but buffer catalysis turned out to be weak in the presence N‐methylhydroxylamine buffer, while it was strong in the presence of acetate and phosphate ones. Buffer‐independent rate constants k₁₀ and k₂₀ increased linearly with the increase in a_OH with definite intercepts. The values of molar absorption coefficient of A , obtained under varying total buffer concentrations at a constant pH, showed the presence of a fast equilibrium: A + CH₃NHOH ? C , where C represents N‐[o‐(N‐methyl‐N‐hydroxycarbamoyl)methyl]benzohydroxamic acid. © 2003 Wiley Periodicals, Inc. Int J Chem Kinet 35: 427–437, 2003     

Temperature, salt and solvent effects on intramolecular general base-catalyzed methanolysis of ionized phenyl salicylate (PS?)

The kinetic characteristics of CO, HC and NO_x reaction on different kinds of three way catalysts (TWC) has been investigated by using a fixed bed reactor. It was concluded that the three-way reaction on noble metal catalysts is controlled by internal diffusion at high space velocity 16×10⁴ h^–1. On non-noble metal catalysts internal diffusion control prevails at space velocities (S.V.) <4×10⁴ h^–1 and kinetic control occurs at S.V.> 4×10⁴ h^–1. On non-noble metal catalysts containing a small amount of a noble metal, the kinetic control region of the three-way reaction shifts to higher space velocity.     

Decolorization and mineralization of textile dyes at solution bulk by heterogeneous nanophotocatalysis using immobilized nanoparticles of titanium dioxide

Nanophotocatalysis using nanostructured semiconductors constitute one of the emerging technologies for destructive oxidation of organics such as dyes. This paper deals with the decolorization and mineralization of reactive dyes by heterogeneous nanophotocatalysis using an immobilized TiO₂ nanoparticle photocatalytic reactor. A simple and effective method was used to immobilization of titanium dioxide nanoparticles. Reactive Orange 107 (RO 107, sulphatoethylsulphonyl reactive dye) and Reactive Red 152 (RR 152, monochlorotriazine reactive dye) were used as model compounds. UV–vis and ion chromatography (IC) analyses were employed to obtain the details of the photocatalytic degradation of the selected dyes. The effects of operational parameters such as H₂O₂, dye concentration, anions (NO₃⁻, Cl⁻, SO₄²⁻, HCO₃⁻ and CO₃²⁻) and pH were investigated. Formate, acetate and oxalate anions were detected as dominant aliphatic intermediates where, they were further oxidized slowly to CO₂. Nitrate, sulfate and chloride anions were detected as the photocatalytic mineralization of RO 107 and RR 152. Kinetics analysis indicates that the photocatalytic decolorization rates can usually be approximated zero-order model for RO 107 and first-order model for RR 152 dyes. Results show that the photocatalytic process occurred at solution bulk and the employment of optimal operational parameters may lead to complete decolorization and mineralization of dye solutions.