3-氯-4-（2-溴甲基-4-甲基-1，3-二恶戍烷-2-基）苯基-4’-氯苯基醚的合成

3-氯-4-（2-溴甲基-4-甲基-1，3-二恶戍烷-2-基）苯基-4’-氯苯基醚是杀菌剂苯醚甲环唑的一个重要中间体。以2-氯-4-（4-氯苯氧基）-苯乙酮为起始原料，采用溴化和合环同时进行的合成工艺制得该化合物，收率90％．产品含量95％。优化了反应条件，简化了操作。     

DXF文件中标题栏及明细表信息获取方法

电力系统企业中大量使用AutoCAD制作的工程图纸,企业实施信息管理系统或ERP系统的过程要求从这些图纸中直接获得其中的物料信息和图纸的一些基本信息。针对这种应用需求简要地分析了DXF文件的格式,然后根据明细表和标题栏的各自不同的特性生成读取信息的方法,该方法可快速地从大量图纸中批量地读取信息,这些信息可以直接为信息管理系统或ERP系统所使用。     

浅谈环保型助溶剂丙二醇醚的现况与应用

简要介绍了丙二醇醚国内外现状以及丙二醇醚的环保性评价和用途。     

Synthesis of polyethylene oxide end‐capped with perfluoroalkyl groups/polystyrene prototype brushes

Polystyrene (PS)/poly(ethylene oxide) (PEO) prototype brushes were prepared by alternating free‐radical copolymerization of methacryloyl‐terminated PS and α‐vinylbenzyl‐ω‐hydroxy or α‐vinylbenzyl‐ω‐perfluoroalkyl (R_f) PEO macromonomers with the addition of Lewis acid (SnCl₄). It was found from their dilute‐solution properties that PS/PEO end‐capped with R_f (PBR_f), and PS/PEO having OH groups at terminal ends (PBOH) prototype brushes formed a single molecule in benzene and aggregates in chloroform, respectively. However, the brush PBOH formed a single molecule in N,N‐dimethylformamide. Such aggregation behaviors seemed to be caused by the interaction between hydroxy groups of PEO chain ends. The brush PBOH was also converted into PBR_f‐type brush by chemical modification, using corresponding acid chloride. The substitution of R_f groups was ～70% due to slipping of terminal hydroxy groups into PEO internal domains. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 772–778, 2006     

黑龙江化肥厂锅炉房用煤车、贮存、运输方案的优化设计

通过对原可行性研究报告中的锅炉房用煤采用筒仓群贮存方案的了解、分析、比较后,提出了采用矩形库贮存煤的优化方案设计的成果。     

一水合硫酸氢钠催化β-萘甲醚的合成

利用一水合硫酸氢钠催化合成 β 萘甲醚 ,3 6 gβ 萘酚 ,3ml甲醇 ,1 5g一水合硫酸氢钠 ,80℃反应5h ,HPLC分析产率达 78 3%。固体催化剂容易过滤分离。     

Synthesis and properties of new polyamides based on a hydroxyethyl cinnamide extended from 3,5‐diaminobenzoic acid

A series of new aromatic polyamides containing cinnamide pendent units were prepared from 2′‐(cinnamide)ethyl‐3,5‐diaminobenzoate and various aromatic dicarboxylic acids by the direct polycondensation reaction, with triphenyl phosphite and pyridine as condensing agents. The polyamides were characterized by ¹H NMR, IR, and UV spectroscopy, and gel permeation chromatography. Their thermal stability was studied by thermogravimetric analysis in air, and differential scanning calorimetry. These polymers were readily soluble in polar aprotic solvents and can be cast from their solutions in flexible and tough films. Glass transition temperatures (T_gs) of these polyamides were observed in the range of 225–245°C. Their inherent viscosities varied from 0.77 to 1.12 dL/g that corresponded to weight–average and number–average molecular weights of 39,000–72,700 and 18,800–29,000, respectively. These polymers can be photochemically crosslinked. The photochemical aspects were revealed by means of UV–vis and IR analyses onto thin films. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2013–2020, 2007     

Tri-pyramid Robot: Design and kinematic analysis of a 3-DOF translational parallel manipulator

3-DOF translational parallel manipulators have been developed in many different forms, but they still have respective disadvantages in different applications. To overcome their disadvantages, the structure and constraint design of a 3-DOF translational parallel manipulator is presented and named the Tri-pyramid Robot. In the constraint design of the presented manipulator, a conical displacement subset is defined based on displacement group theory. A triangular pyramidal constraint is presented and applied in the constraint designs between the manipulator?s subchains. The structural properties including the decoupled motions, overconstraint elimination, singularity free workspace, fixed actuators and isotropic configuration are analyzed and compared to existing structures. The Tri-pyramid Robot is constrained and realized by a minimal number of 1-DOF joints. The kinematic position solutions, workspace with variation of structural parameters, Jacobian matrix, isotropic and dexterity analysis are performed and evaluated in the numerical simulations.     

Mechanical properties of a cryogenically mechanically alloyed polycarbonate–poly(aryl ether ether ketone) system

The processing–property relationship of a model cryogenically mechanically alloyed polymer–polymer system [polycarbonate (PC) and poly(aryl ether ether ketone) (PEEK)] was investigated. PC and PEEK powders were cryogenically mechanically alloyed for 10 h, and the resulting two‐phase powder particles were processed into testable coupons with a miniature ram‐injection molder. The bulk mechanical properties of the coupons made from the mechanically alloyed powders and nonmechanically alloyed powders were investigated as a function of mechanical alloying and injection‐molding parameters. The injection‐molded coupons were mechanically tested in the three‐point‐bending mode. The results demonstrated that no measurable improvement was achieved in the energy to break, strain at failure, or failure strength in the coupons made from the mechanically alloyed materials in comparison with those of the coupons made from the nonmechanically alloyed powders. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1196–1202, 2003