STUDY ON THE CARDANOL-ALDEHYDE CONDENSATION POLYMER CONTAINING BORON-NITROGEN COORDINATE BOND

Cardanol-aldehyde condensation polymer containing boron-nitrogen coordinate bond (CFBN) has been synthesized and characterized by IR, XPS, HPLC and DTA-TG. Its properties were also investigated. The results show that the coating film of CFBN has excellent physico-mechanical properties, good anticorrosive properties and stable at high temperature. (Author abstract) 8 Refs.

Syntheses,crystal structures,and catalytic properties of three zinc(Ⅱ),cobalt(Ⅱ)and nickel(Ⅱ)coordination polymers constructed from 5⁃(4⁃carboxyphenoxy)nicotinic acid

Three zinc(Ⅱ),cobalt(Ⅱ),and nickel(Ⅱ)coordination polymers,namely[Zn(μ^(3-)cpna)(μ-dpea)_(0.5)]_(n)(1),[Co(μ^(3-)cpna)(μ-dpey)_(0.5)]_(n)(2),and[Ni(μ^(3-)cpna)(μ-dpey)_(0.5)(H_(2)O)]_(n)(3),have been constructed hydrothermally using H_(2)cpna(5-(4-carboxyphenoxy)nicotinic acid),dpea(1,2-di(4-pyridyl)ethane),dpey(1,2-di(4-pyridyl)ethylene),and zinc,cobalt,and nickel chlorides at 160℃.The products were isolated as stable crystalline solids and were characterized by IR spectra,elemental analyses,thermogravimetric analyses,and single-crystal X-ray diffraction analyses.Single-crystal X-ray diffraction analyses revealed that three compounds crystallize in the triclinic system,space group P1.Compounds 1-3 show 2D layer structures.The catalytic activities in the Knoevenagel condensation reaction of these compounds were investigated.Compounds 1 and 2 exhibit effective catalytic activities in the Knoevenagel condensa-tion reaction at room temperature.For this reaction,various parameters were optimized,followed by the investiga-tion of the substrate scope.CCDC:2335676,1;2335677,2;2335678,3.

Heat Transfer Characteristics of Dropwise Condensation of Steam on Vertical Polymer Coated Plates

The plasma polymerization method and dynamic ion-beam mixed implantation method were employed to coat ultra-thin polymer films on copper plates. Experiments indicated that steady dropwise condensation of steam at atmospheric pressure occurred. The condensation heat transfer coefficients increased by approximately 3 and 5－7 times for the polytrimethylvinylsilane film and polytetrafluoroethylene film respectively, compared with the value for film condensation under the same experimental conditions. The temperatures on the condensing surface and inside the test block were found to be rapidly and randomly fluctuated. The properties of the coated films and advantages of the methods used in this investigation were discussed briefly.

Insertion of pillar[5]arene into Troger’s base-derived porous organic polymer for promoted heterogeneous catalytic performance in Knoevenagel condensation and CO_(2)fixation

Development of new metal-free heterogeneous catalysts has long been the focus of intense research interest.The integration of multifunctional monomers into the skeletons of porous organic polymers(POPs)provides an efficient pathway to achieve this goal.Herein,we rationally designed and successfully prepared a new Troger’s base(TB)-derived POPs by insertion of pillar[5]arene macrocycle as a positively auxiliary group.Combined the both merits of pillar[5]arene macrocycle and TB moiety,the as-prepared polymer was further explored as an effective metal-free heterogeneous catalyst and exhibited promoted catalytic performance in Knoevenagel condensation and CO_(2)conversion.This work provides a new strategy to fabricate metal-free heterogeneous catalysts based on macrocyclic POPs.

SYNTHESIS OF SPHERICAL MACROPOROUS ADSORBENT BASED ON UREA-FORMALDEHYDE CONDENSED POLYMER

Spherical macroporous adsorbents with active sites capable of hydrogen bonding adsorption based on urea-formaldehyde condensed polymer were synthesized via reversed suspension polymerization. The properties of the obtained adsorbent were also investigated in detail. The results showed that the water permeability could be improved by adding hydroxyl-containing organic compound moiety into the adsorbent. The specific surface area and average pore diameter of these adsorbents increased while the porosity first increased then decreased with the increase of the amount of the added hydroxyl-containing compound.

Studies on the Self-condensing Vinyl Polymerization of a Novel Maleimide Inimer

The self-condensing vinyl polymerization(SCVP) of a novel maleimide inimer(initiator-monomer) 1, N-(4-α-bromobutyryloxy phenyl) maleimide with the complex of CuBr/Bipy(2, 2′-bipyridine) as the catalyst was studied. GPC was used to determine the molecular weight and the results show that the molecular weight increases exponentially with polymerization time during the first hour, and then the rate of increase molecular weight slows down. The molecular weight also increases with increasing dosage of the catalyst. The coincidence of the molecular weights determined by 1H NMR and GPC proves that the polymer obtained from the SCVP of inimer 1 has a linear structure, which is further verified by 13C NMR spectrum. A hyperbranched polymer was obtained by the copolymerization of inimer 1 and styrene.

ADSORPTION OF PHENOLIC COMPOUNDS ONTO THE SPHERICAL MACROPOROUS ADSORBENT BASED ON UREA-FORMALDEHYDE CONDENSED POLYMER

Absorption of phenol, catechol and resorcinol. which vary in their ability to interact with the adsorbent through hydrogen bond, were used to investigate the adsorption mechanistic interaction. The adsorption enthalpies of the above mentioned compound onto the adsorbent were calculated and thermodynamic analysis was carried out. The results showed the adsorbent with the lowest adsorption enthalpies for the sorbate such as catechol with intermolecular hydrogen bond also display the lowest adsorption affinity On the other hand the more of the groups available for hydrogen bond interaction. the higher of the adsorption affinity These observations support the contention that phenol adsorption is driven predominantly by specific interaction of the solute with active sites on the surface of the adsorbent.

Synthesis of Highly Branched Poly(ε-caprolactone) by Self-condensing Atom Transfer Radical Polymerization of Macroinimers

Branched poly（ε-capmlactone） was synthesized by self-condensing atom transfer radical polymerization of macroinimer, α-acryloyoxy-ω-2-bromopropionyloxy poly（ε-caprolactone）, which was prepared by enzyme-catalyzed ring-opening polymerization of ε-caprolactone with 2-hydroxylethyl acrylate as initiator and esterification of the ω-hydroxyl group of the obtained poly（ε-caprolactone） by 2-bromopropionyl bromide.

Filmwise Condensation Heat Transfer Enhancement with Dropwise and Filmwise Coexisting Condensation Surfaces

Six surfaces were prepared with defferent surface division patterns for the experimental investigationof steam condensation heat transfer characteristics for dropwise and filmwise coexisting(DFC)condensationsurfaces under atmospheric pressure Dropwise condensation(DWC)was promoted with an ultrathin polytetrafluoroethylene(PTFE)film,which was prepared by the dynamic ion-beam mixed implantation(DIMI)method.The results showed that the condensation phenomena at the intersection between the dropwise andfilmwise condensation regios were quite different for different relative positions of the dropwise and filmwisecondensation regions.The experimental results revealed that the condensation heat transfer characteristics werehighly influenced by the surface division number and the relative area ratio of the dropwise and filmwise conden-sation regions.The impact of thesc findings on heat transfer enhancement mechanism for condensation heattransfer is discussed in detail.

Rheological property of low-damage,ideal packing,film-forming amphoteric/sulfonation polymer drilling fluids

Low-permeability dense reservoirs,including micro-fractured reservoirs,are commonly characterized by high content of clay substances,high original water saturation,high sensitivity to invasive fluids,high capillary pressure,complicated structure and anisotropic,high flow-resistance and micro pore throats etc,.Generally they also have lots of natural micro fractures,probably leading to stress sensibility.Main damaging factors in such reservoirs are water-sensibility and water-blocking caused by invasive fluids during drilling and production operations.Once damaged,formation permeability can rarely recovered.Numerous studies have shown that damaging extent of water-blocking ranges from 70% to 90%.Main damaging mechanisms and influencing factors of water-blocking were systematically analyzed.Also some feasible precaution or treating approaches of water-blocking were put forward.In a laboratory setting,a new multi-functional drilling fluid composed mainly of amphion polymer,sulfonation polymer,high effectively preventive water-blocking surfactants,ideal packing temporary bridging agents(TBA) and film-forming agents,etc.,were developed.New low-damage drilling fluids has many advantages,such as good rheological properties,excellent effectiveness of water-blocking prevention,good temporary plugging effect,low filtration and ultra-low permeability(API filtration≤5 mL,HTHP filtration≤10 mL,mud cake frictional coefficient≤0.14,permeability recovery>81%),can efficiently prevent or minimize damage,preserve natural formation and enhance comprehensive development-investment effect in TUHA Jurassic dense sandstone reservoir formation with low-permeability,the only one developing integrated condense gas field.Some references can be provided to similar reservoir formations.

Poly(ethylene glycol)-supported Piperazine——Synthesis and Application in Knoevenagel Condensation

A soluble, poly（ethylene glycol）-supported piperazine catalyst was prepared. This soluble catalyst efficiently catalyzes the Knoevenagel condensation of various aromatic aldehydes with diethyl malonate or ethyl acetoacetate in a homogeneous phase to afford the desired alkenes in good purity and yield with a facile work-up process. It was found that the polymer reagent could be repeatedly used at least four times without the too much loss of activity. The catalyst has shown a good activity, stability, and recycling capability.

Thermal Properties of Poly（vinyl chloride-co-vinyl acetate-co-2-hydroxypropyl acrylate） （PVVH） Polymer and Its Application in ZnO Based Nanogenerators ：

A novel piezoelectricity based nano energy conversion device using vertically aligned ZnO nanowires/PVVH matrix as the working unit is proposed. Thermal energy is converted to electricity via the interaction of the PVVH polymer and ZnO nanowires. The thermal properties of PVVH ave studied using Raman spectroscopy under different temperatures. The results show that the structure of PVVH is sensitive to fluctuations of the environmental temperatures. With the increasing temperature, PVVH tends to be crystallized and stress can be developed inside the polymer. The stress is responsible for the deformation and voltage generation of the ZnO nanowires.

Effect of Poly（Ether Urethane） Introduction on the Performance of Polymer Electrolyte for All-Solid-State Dye-Sensitized Solar Cells

The introduction of poly（ether urethane） （PEUR） into polymer electrolyte based on poly（ethylene oxide）, LiI and I2, has significantly increased the ionic conductivity by nearly two orders of magnitudes. An increment of I3- diffusion coefficient is also observed. All-solid-state dye-sensitized solar cells are constructed using the polymer electrolytes. It was found that PEUR incorporation has a beneficial effect on the enhancement of open circuit voltage VOC by shifting the band edge of TiO2 to a negative value. Scanningelectron microscope images indicate the perfect interfacial contact between the TiO2 electrode and the blend electrolyte.

A Novel Biodegradable Poly (Hydroxybutanedioic Acid-co-2-hydroxypropane-1,2,3-tricarboxylic Acid) Copolymer for Water Treatment Applications

Minimizing the formation of inorganic scale deposits in industrial water continues to be a challenge for water treatment systems. In order to meet this challenge a novel biodegradable poly (DL-malic acid-co-citric acid) copolymer, effective in providing calcium carbonate scale inhibition was developed. Synthesis and characterization of the biodegradable, water-soluble and polyester copolymer was performed. Synthesis was done by direct bulk melt condensation in the absence of a catalyst above 150°C. Characterization of the copolymer was carried out using infrared absorption spectra (FTIR), differential scanning calorimetry (DSC) and thermo gravimetric analysis (TGA) equipment. In the present work the precipitation of calcium carbonate from relative supersaturated solutions at different weight ratios of comonomer inhibition rates have been studied. The results indicate that the copolymer is an effective calcium carbonate descaling inhibitor that suppresses the growth process against calcium mineral scale deposits.

《高分子凝聚态物理》课程改革探索

《高分子凝聚态物理》是高分子专业方向研究生基础课程,对培养高分子专业人才具有重要的作用,本文将高分子理论与科研实践紧密结合,旨在培养学生的科研创新潜力和社会责任感。针对不同育人目标,设计了多样化的教学过程,采用现代教育工具和实例引导学生思考课程内容的应用和意义,并探讨了如何通过适当的设计和评价方法实现这一目标。

基于5-(2-羧基苯基)吡啶-3-甲酸配体的镍(Ⅱ)和锌(Ⅱ)配位聚合物的合成、晶体结构、催化及抗磨性质

采用水热方法,选用5-(2-羧基苯基)吡啶-3-甲酸配体(H_(2)cpna)与1,2-二(4-吡啶基)乙烷(dpea)或1,2-二(4-吡啶基)乙烯(dpey)分别与NiCl_(2)·6H_(2)O和ZnCl_(2)在160℃下反应,合成了2个三维配位聚合物{[Ni(μ3-cpna)(μ-dpea)_(0.5)]·H_(2)O}n (1)和{[Zn(μ_(3)-cpna)(μ-dpey)_(_(0.5))]·H_(2)O}_n (2),并对其结构、催化和摩擦性质进行了研究。研究表明,在室温条件下化合物2在Knoevenagel缩合反应中显示出较好的催化活性。同时,2在聚α-烯烃合成润滑剂中显示出有效的抗磨性能。

新工科背景下高分子材料的凝聚态结构表征方法研究生课程建设探索与实践

为了满足新工科建设对卓越工程创新人才培养的要求,高分子材料的凝聚态结构表征方法课程教学团队进行课程建设和教学改革。文章分析了高分子材料专业研究生创新能力培养过程中存在的问题,从教学内容和方法、课程思政及考核方式等方面介绍了该课程的教学改革实践。教学改革有效激发了学生的学习兴趣,并取得了一些初步的成效。

卧式捏合反应器及其在聚合工业中的研究进展

卧式捏合反应器具有大的反应体积,优异的混合性能、表面更新性能、传热性能和自清洁性能,因而在本体聚合、缩合聚合和聚合物脱挥等领域具有广阔的应用前景。综述了几种捏合反应器及其搅拌特性研究,以及在聚合工业中的应用研究,指出捏合反应器具有非常复杂的几何结构,实验测量技术具有很大的局限性,计算流体力学(CFD)模拟为主要的研究方法;进一步指出具有自清洁特性的捏合反应器是聚合物搅拌设备开发的主要方向,高效、集约化、绿色、环保的先进工艺与装置是促进我国聚合工业发展的关键。

Molecular weight distribution of A_2-B_2 type condensation polymers in the presence of capping monomer C

The molecular weight distribution of A2-B2 type condensation polymers in the presence of capping monomer C has been derived with statistical calculation and Monte Carlo simulation methods. The Monte Carlo simulation result agrees with that of statistical calculation. The number distribution function and weight distribution function of seven types of molecules existing in A2-B2-C system have been obtained. The effect of reactivity of capping monomer C on these distributions are discussed.

MOLECULAR WEIGHT DISTRIBUTION OF AB, A, TYPE CONDENSATION POLYMERS OBTAINED BY ADDING AB MONOMERS IN BATCHES

The molecular weight distribution (MWD) and arm length distribution of AB, Ar type condensation polymers obtained by adding AB monomers in batches have been derived by statistical and kinetic methods. Calculations show the MWD of condensation polymers obtained by this process is much narrower than that of one batch reaction and agrees with the Monte Carlo results very well.