水泥砂浆增强剂丙烯酸酯乳液的研制

混凝土材料的多孔性和易产生裂纹等问题影响了混凝土材料和结构的耐久性,导致了混凝土结构出现过早劣化,极大地影响了混凝土设施的正常使用。用水泥砂浆增强剂配制的新型混凝土材料——聚合物改性水泥砂浆具有很好的防渗性、防裂性、耐磨性、粘附性以及压缩和拉伸强度高等优点,已广泛用于建造高结构强度、高抗震、高质量和长久寿命的建筑。     

Flows of dilute hydrolyzed polyacrylamide solutions in porous media under various solvent conditions

Experimental results on pressure losses of flows of dilute polymer solutions through porous media are summarized. The polymer products employed in this study consisted of partially hydrolyzed polyacrylamides (HPAM) with different degrees of hydrolysis. The effect of the hydrolysis on the pressure drop is investigated in a porous media test section designed to minimize polymer degradation. The investigations were carried out for various solvent conditions, and it is shown that the maximum increase in pressure drop is mainly dependent on the molecular weight of the polymers. The onset of the polymer action is measured for various fluid and solvent properties. Particular attention is given to measurements near θ-conditions. The results stress the importance of the solvent properties on the actions of the polymers and on the resultant pressure drop for porous media flows. The addition of salt ions to solutions of partially hydrolyzed polyacrylamides yields onset behavior previously observed for nonionic polymers. The differences measured between various solvent properties can be explained by the actual hydrodynamic molecule dimensions for a given molecular weight and polymer concentration. To quantify the influences of the solvent properties on the polymers, measurements were carried out in aqueous solutions for various pH values and therefore at various degrees of dissociation. The importance of separating polymer effects caused by their linear dimension in the solution from those that are introduced by and increase in solvent viscosity is shown. Measurements were performed to quantify the effects of solvent viscosity on the polymer action and to separate these effects from those due to changes in molecule dimensions. The implications of the present results are stressed in connection with applications of polymer solutions in tertiary oil recovery, and the positive features of the molecule actions on flow in such applications are described.     

Capillary breakup extensional rheometry of associative and hydrolyzed polyacrylamide polymers for oil recovery applications

High molecular weight polymers used for heavy oil recovery exhibit viscoelasticity that can influence the oil recovery during chemical enhanced oil recovery. Different polymers having similar molecular weight and shear rheology may have different elongation flow behavior depending on their extensional properties. Displacing slugs are more likely to stretch than shear in tortuous porous media. Therefore, it is critical to seek an analytical tool that can characterize extensional parameters to improve polymer selection criteria. This article focuses on the extensional characterization of two polymers (hydrolyzed polyacrylamide and associative polymer) having identical shear behavior using capillary breakup extensional rheometer to explain their different porous media behavior. Maximum extensional viscosity at the critical Deborah number and Deborah number in porous media classified the associative polymer as the one having high elastic‐limit. Extensional characterization results were complemented by significantly higher pressure drop, marginally increased oil recovery of associative polymer in porous media. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46253.     

Porous materials from crystallizable polyolefins produced by gel technology

A new method for obtaining porous and porous fiber polymers is presented. This method is based on using gel-type technology (without previously preparing polymer solutions) for crystallizable polymers, preparing polyethylenes, and including polyethylenes of very high molecular mass and isotactic polypropylene. The method consists in swelling crystalline polymer films at elevated temperatures in a proper solvent with subsequent precipitation with a non-solvent at different conditions. In this case, simultaneous or consecutive processes of phase separation of amorphous or/and crystalline type occurs; stretching the sample can also accompany this process. Complete phase diagrams of two- and three-component systems (polymer-solvent and polymer-solvent precipitator) were constructed. Temperature-concentration boundaries of amorphous separartion (binodal) and crystallization (liquidus) are reported for the system polyethylene? o-xylene? dimethyl formamide. Phase transitions of both types influence characteristics of the resultant porous structure. They were prepared by simultaneous (precipitation of a gel by dimethyl formamide at 25°C) or consecutive (precipitation with a hot non-solvent at 138°C and following cooling) phase separation. Studied were the effect of experimental conditions (temperature, times for solvation and precipitation, polymer molecular mass, the thermodynamic quality of solvents and parameters of film stretching) on peculiarities of the structure and quantitative characteristics of final porous and fiber-porous polyolefins. It has been demonstrated that the method proposed allows us to obtain a crystalline and highly porous polymer with open poros, a bimodal size distribution and with a highly developed inner surface. Further high strength and small shrinkage are characteristic of the fiber-porous materials. The method under discussion appears to be universal, it does not require a preliminary preparation of polymer solutions and can be realized within a general technology of polymer films and sheet processing. Highly porous polymers obtained by this technology, primarily based on polyethylenes of very high molecular mass, can be used as neutral supports for multi-functional membranes, polymeric covers, frame systems for implants and other applications.     

Synthesis,Characterisation, and Evaluation of a Cross-Linked Disulphide Amide-Anhydride-Containing Polymer Based on Cysteine for Colonic Drug Delivery

The use of disulphide polymers, a low redox potential responsive delivery, is one strategy for targeting drugs to the colon so that they are specifically released there. The objective of this study was to synthesise a new cross-linked disulphide-containing polymer based on the amino acid cysteine as a colon drug delivery system and to evaluate the efficiency of the polymers for colon targeted drug delivery under the condition of a low redox potential. The disulphide cross-linked polymers were synthesised via air oxidation of 1,2-ethanedithiol and 3-mercapto-N-2-(3-mercaptopropionamide)-3-mercapto propionic anhydride (trithiol monomers) using different ratio combinations. Four types of polymers were synthesised: P10, P11, P151, and P15. All compounds synthesised were characterised by NMR, IR, LC-MS, CHNS analysis, Raman spectrometry, SEM-EDX, and elemental mapping. The synthesised polymers were evaluated in chemical reduction studies that were performed in zinc/acetic acid solution. The suitability of each polymer for use in colon-targeted drug delivery was investigated in vitro using simulated conditions. Chemical reduction studies showed that all polymers were reduced after 0.5–1.0 h, but different polymers had different thiol concentrations. The bacterial degradation studies showed that the polymers were biodegraded in the anaerobic colonic bacterial medium. Degradation was most pronounced for polymer P15. This result complements the general consensus that biodegradability depends on the swellability of polymers in an aqueous environment. Overall, these results suggest that the cross-linked disulphide-containing polymers described herein could be used as coatings for drugs delivered to the colon.     

Tough reinforced open porous polymer foams via concentrated emulsion templating

Low-density but very resilient and robust polymer foams possessing an interconnected open porous network have been synthesised by the polymerisation of the continuous phase of concentrated or high internal phase emulsions containing polyethylene glycol dimethacrylate (PEGDMA) as main crosslinker. The synthesised polymer foams did not display the undesirable properties, such as brittleness and chalkiness, which are commonly observed for highly crosslinked porous polymer monoliths synthesised by the polymerisation of high internal phase emulsions. An effective way to improve the mechanical performance of open porous polymer foams is to raise the apparent foam density. Therefore, the continuous phase of the emulsions was increased up to 40 vol.%. The mechanical properties can be further increased by the incorporation of silica particles into the polymer. Methacryloxypropyltrimethoxysilane was added to the continuous phase to ensure that the silica particles were covalently bonded into the inorganic polymer network formed by the hydrolytic condensation of the silane groups. The addition of reinforcement increased the mechanical properties. The Young's modulus and the crush strength of the polymer foams increased by up to 360% and by up to 300%, respectively, in comparison to non-reinforced samples.     

Synthese elektrisch leitfähiger polymerer

Synthesis of electrically conducting polymers In the last few years electrically conducting polymers have been a centre of scientific interest. Characteristic of these polymers - e. g. polyenes and polyaromatics - are their conjugated double bonds. The addition of electron donators or acceptors causes by the change from insulator properties to electrical conductivity comparable to that of metallic conductors oxidation or reduction of the polymer backbone. Via complex formation a considerable increase in the electron mobility and electrical conductivity is obtained. The aim of the polymer chemist is the synthesis of electrically conducting polymer backbones. An abundance of synthetic routes is available. In addition to the conventional stepwise synthesis using the Wittig-, Horner or Grignard reactions, polycondensation processes and metal-catalysed polymerisat ion techniques can be employed. Oxidative coupling with oxidising Lewis acid catalysts generally leads to polymers with aromatic or heterocyclic units. The Ziegler-Natta-polymerization of acetylenes to filmbuilding polyacetylenes has found broad acceptance; it represents however only one of the many possible reactions, in which reducing agents in combination with transition metals are catalytically active. The polymers synthesised via this process are made electrically conducting by doping. On the other hand the direct polymerisation process e.g. starting from acetylene or aromatics, using the doping agent or via anodic oxidation e. g. from pyrrole, leads directyl to materials with a high electrical conductivity. This paper contains the most important publication with the exception of the patents in the intensively researched field of the synthesis of aliphatic and aromatic polymers with π-electron-conjugation as well as their doping to highly conducting materials.     

A paint removal concept with side-chain liquid crystalline polymers as primer material

A new paint removal concept is introduced making use of a polymer primer layer with a sharp softening temperature. For this, a new class of side-chain liquid crystalline polymers with polar moieties in the backbone has been developed and studied in thin films. These polymers form lamellar-ordered mesophases and contain adhesion-enhancing moieties, which can provide protection against corrosion. Furthermore, the polymers possess phase transitions which are accompanied by drastic changes in the mechanical properties. When the viscosity of a primer film abruptly drops it will start to flow which makes it possible to remove the coating layer as an intact film, simply by pulling the coating off the primer layer. Since the various synthesised polymers all possess different transition temperatures, we can choose the most convenient polymer on the basis of the desired temperature dependence.     

Supercritical CO2-assisted preparation of a PMMA composite membrane for bisphenol A recognition in aqueous environment

This work reports a novel strategy to prepare affinity composite membranes using supercritical fluid technology. By blending molecularly imprinted polymeric particles with PMMA, a porous hybrid structure with affinity to the template molecule, bisphenol A, was prepared using a supercritical carbon dioxide (scCO₂)-assisted method. Membranes were characterized in terms of morphology, mechanical performance and transport properties. The ability of the polymers and hybrid membranes to adsorb bisphenol A was tested in aqueous solutions and fitted to a linearized Langmuir equation, showing that adsorption takes place at homogeneous affinity binding sites within the imprinted surface. Filtration experiments showed that the imprinted hybrid membrane was able to adsorb higher amounts of template even in non-equilibrium dynamic binding conditions. The hybridization of the PMMA membrane herein reported conveys two important improvements over neat PMMA membrane: it introduced molecular affinity towards the template molecule and significantly increased the permeability of the porous structures, which are key parameters in processes that involve membranes. This technique could expand the applications of polymeric beads powders and enhance the efficiency of the membrane's transport properties. Our work presents a new method to confer affinity to a porous structure by immobilization of imprinted polymers, combining polymer synthesis and membrane formation using supercritical fluid technology.     

Effect of the Molecular Weight of Fibre-Forming Polymers on the Mechanical Properties of Polymer Fibres (Review)

The effect of the molecular weight of fibre-forming flexible- and rigid-chain polymers on the strength properties of fibres made from them is examined. It was shown that in contrast to high-strength flexible-chain polymer fibres, for which the use of polymers with ultrahigh molecular weights of several million is a necessary condition for sharply increasing the strength, polymers with a normal molecular weight of 20,000-60,000 are used for fabricating high-strength fibres from rigid-chain polymers. Increasing the molecular weight of aromatic polymers during synthesis or by solid-phase afterpolycondensation conducted on the polymer or finished fibre can significantly increase the strength of the fibres.     

Thermal and catalytic aspects of Ln(III) polymer–metal complexes

BACKGROUND: In this era, polymer‐supported catalysts are gaining more attention, as they are effective in reduction of pollution, production cost and give good yield. Due to the versatility of lanthanide catalysts in organic synthesis, we envisioned that lanthanides(III) supported polymers would afford a novel type of solid phase Lewis acids. RESULTS: The polymer–metal complexes are found to be efficient and effective catalysts in the Biginelli three‐component, one‐pot synthesis of 3,4‐dihydropyrimidin‐2(1H)‐ones. The synthesized polymer is thermally more stable and porous in nature than polychelates. CONCLUSION: The polymer–metal complexes can be used as economical and eco‐friendly catalysts for synthesis of substituted 3,4‐dihydropyrimidin‐2(1H)‐ones with different aromatic aldehydes and β‐ketoesters. Thermal stability of the polymer is higher than that of polychelates due to the presence of intramolecular hydrogen bonding. Copyright © 2009 Society of Chemical Industry     

Effects of the side chain density of polycarboxylate dispersants on dye dispersion properties

Comb‐like polycarboxylates were synthesised by copolymerisation of methacrylic acid and nonylphenol polyethylene glycol methacrylate ester, and can be used as dye dispersants. In order to achieve good dispersive ability, three polycarboxylates were synthesised, each having a different side chain density. The side chain density of polymers was controlled by different ratios of monomers in the copolymerisation process. Acidic polymers were neutralised using sodium hydroxide. These polymers exhibit good dispersing performance, such that carboxylate groups are adsorbed onto the dye particle surface and the side chains enable the formation of a thick layer, thus providing the steric hindrance effect. Improvement of dye dissolution in the presence of polycarboxylates was studied. Polymers with a lower side chain density demonstrated a higher dye dissolution in water, which could be as a result of more effective adsorption of dispersant on the dye surface (CI Disperse Blue 79). The dyeing performance of the prepared dye dispersions on polyester was investigated. Spectrophotometric analysis of dyed fabrics using synthesised polycarboxylates demonstrates that there should be an optimum side chain density of polymer in order to control both dye solubility and dispersive ability. The result of turbidimetry and particle size analysis have proven this phenomenon. A comb‐like polycarboxylate with optimum side chain density was a better dye dispersant compared with a commercial sodium naphthalene sulphonate compound, as a result of its better heat stability.     

Design and synthesis of porous polymeric materials and their applications in gas capture and storage: a review

The design and synthesis of porous organic materials that have increasing physical and chemical characteristics have been discussed. For example, a variety of porous organic polymers, metal–organic frameworks, conjugated microporous polymers, and polymers of intrinsic microporosity have been designed and synthesized using simple and efficient procedures. Such materials have unique gas adsorption properties and can be used in gases separation and storage. In addition, they have high surface area, porosity, and selectivity towards carbon dioxide compared to other gases such as nitrogen and methane.     

SINGLE FLUID FLOW IN POROUS MEDIA

A comprehensive study on single fluid flow in porous media is carried out. The volume averaging technique is applied to derive the governing flow equations. Additional terms appear in the averaged governed equations related to porosity ε, tortuosity τ, shear factor F and hydraulic dispersivity D _h. These four parameters are uniquely contained in the volume averaged Navier-Stokes equation and not all of them are independent. The tortuosity can be related to porosity through the Brudgemann equation, for example, for unconsolidated porous media.

The shear factor models are reviewed and some new results are obtained concerning high porosity cases and for turbulent flows. It is known that there are four regions of flow in porous media: pre-Darcy's flow, Darcy's flow, Forchheimer flow and turbulent flow. The transitions between these regions arc smooth. The first region, the pre-Darcy's flow region represents the surface-interactive flows and hence is strongly dependent on the porous media and the flowing fluid. The other flow regions are governed by the flow strength of inertia. For Darcy's flow, the pressure gradient is found to be proportional to the flow rate. The Forchheimer flow, however, is identified by a strong inertia! effects and the pressure gradient is a parabolic function of flow rate. Turbulent flow is unstable and unsteady flow characterized by chaotic flow patterns. The pressure drop is slightly lower than that predicted using the laminar flow equation.

The hydraulic dispersivity is a property of the porous media. It may be considered as the connectivity of the pores in a porous medium. It characterizes the dispersion of mementum, heat and mass transfer. In this paper, only the dispersion of momentum is studied.

Single fluid flow through cylindrical beds of fibrous mats and spherical particles has been used to show how to solve the single fluid flow problems in porous media utilizing the knowledge developed in this communication. Both the pressure drop and axial flow velocity profiles are computed using the developed shear factor and hydraulic dispersion models. Both the predicted velocity profile and pressure drop compare fairly well with the published experimental data.     

超临界流体增强聚酯薄膜中的质量传递

聚合物中杂质/挥分的存在对聚合物的终端使用将产生负面影响,因此必须将其除去.传统的脱挥方法效率有限,使用超临界流体技术可增强脱挥效率.测定了温度为343 K、压力为30 MPa、CO₂流量为4.0 L•min^-1条件下,PET聚酯薄膜中的乙二醇单体挥分含量与时间的关系,以研究聚合物系超临界流体脱挥过程中的质量传递规律;根据传质理论建立了一个理想的超临界流体脱挥过程的质量传递模型,并用该模型分析处理实验数据,结果表明该模型较好地反映了聚合物系超临界流体脱挥过程的基本特征.     

Characterization of polymer adsorption in tube flow of drag reducing fluids

Elucidation of the polymer adsorption and flow characteristics at the tube wall is essential for an understanding of turbulent drag reduction. The polymer adsorbed onto the tube wall, in the flow of dilute solutions of linear random coiling macromolecules, also produces a concentrated fluid layer at the surface of the adsorption zone, as a result of the flow of the solvent micromolecules in the porous network comprising the adsorption zone.Velocity profiles are developed and used to determine the radial variation in the adsorption zone of porosity, as well as fractional surface coverages and mean separation or interpenetration distances between macromolecules in the various adsorption layers. The polymer concentration build-up in the concentrated fluid layer is also evaluated. Predictions of the latter for aqueous Polyox WSR-301 solutions are in qualitative agreement with experimental measurements and suggest that turbulent drag reduction is related to the level of polymer build-up in the concentrated fluid layer.     

Non-equilibrium chemical potential and polymer extraction from a porous matrix

The influence of a flow on the transfer of a polymer solution from a porous matrix to a flowing fluid is analysed. Since the flow modifies the free energy of the solution, through stretching and orientation of the macromolecules, the thermodynamic driving force for polymer transport is modified with respect to that of a quiescent fluid. The consequences of this modification for the extraction of a polymer from a porous matrix are explored in detail, and the formal results are explicitly illustrated by means of a specific solution. For the particular example analysed here, of possible interest in oil extraction or in microfluidic problems, the non-equilibrium effects may yield a reduction of the order of 10% of the extraction rate.     

多孔介质中流体流动的格子气自动机模拟

介绍了 13-Bit正六边形多速格子气自动机模型的特点 ,讨论了多孔介质流体流动的格子气自动机模型的渗透率等参量算方法 ,应用该模型对计算机产生的多孔介质几何构型和焦炭多孔介质中的流体流动进行了模拟 ,其结果既可以给出多孔介质中的流动细节 ,也可统计得到表征多孔介质宏观流动特征的物理参量 .初步研究表明 :格子气自动机模型可用于模拟复杂边界条件下多孔介质的流体流动     

The effect of polymerisation methods on the adsorption capacity of HEMA based molecularly imprinted polymers

Molecularly imprinted polymers (MIPs) are generally synthesised either by thermal initiation or by photo polymerisation methods. Recently we used a gamma irradiation method for the preparation of MIPs. In this communication we compare three different methods for the synthesis of 2-hydroxy ethyl methacrylate (HEMA) based MIP imprinted for hydrocortisone in terms of its capacity to adsorb the print molecule. Our results show that MIP prepared by the gamma irradiation method has a better adsorption capacity than the thermally initiated polymer. It is interesting to note that its adsorption capacity is comparable or marginally better than the photo polymerised MIP.     

Mold-filling simulations for the injection molding of continuous fiber-reinforced polymer

Injection molding can be used to fabricate fiber-reinforced polymer composites by impregnating a continuous fabric mat preplaced in a mold cavity with a polymer resin. The mold-filling time is dependent on the flow and heat transfer behavior in the mold. A model is proposed that considers the non-Newtonian How through the porous fabric mat and the heat transfer between mold, fabric mat, and flowing fluid. The model was simulated for the mold filling of a carbon fiber mat with a pseudoplastic polymer solution. The results from the simulation provide Information for optimizing mold-filling parameters through proper selection of inlet fluid pressure, heat source temperature, and type of polymer-solvent system.