羧基改性聚乙烯醇的制备及水溶性研究

通过丙烯酸(AA)与乙酸乙烯酯(VAc)共聚进而醇解的方法合成出具有高醇解度、低结晶度的丙烯1酸改性聚乙烯醇。通过FT-IR和H-NMR对聚合物的化学结构进行了表征;通过XRD、UV-Vis、剪切流变测试等手段研究了丙烯酸结构单元含量对改性PVA的结晶性能、水溶性能和溶液表观黏度的影响。结果显示,通过引入适量丙烯酸结构单元,可降低PVA结晶度,提高PVA水溶性,增强PVA水溶液表观黏度的剪切稳定性。     

脂肪醇醚化接枝聚乙烯醇合成高耐水性树脂

采用聚乙烯醇(PVA)与脂肪醇进行醚化接枝反应,通过红外光谱分析和对接枝聚合物耐水性能测试研究了从不同的脂肪醇,反应温度、反应时间及反应物配比对产物的影响。通过正交实验方法确定了最佳反应条件:以浓H2SO4为催化剂,二甲亚砜为醚化溶剂、正辛醇为醚化剂,醚化反应温度120℃、反应时间2h、PVA与正辛醇物质的量比为1∶1.2。在此反应条件下合成的接枝聚合物耐水性能最好,蒸馏水抽提后的余重高达98.03%,属高耐水性树脂。     

泡花碱和己二异氰酸酯同时对聚乙烯醇胶水改性的研究

采用正交实验法探讨己二异氰酸酯(HDI)和泡花碱共同对聚乙烯醇(PVA)胶水进行交联改性。讨论其反应的原理、合成方法、粘结性能及其耐水性能。本研究结果获得一种耐水性能和粘结性能优良的聚乙烯醇类粘合剂。     

Production of cellulose nanofibers from Alfa grass and application as reinforcement for polyvinyl alcohol

The work reported demonstrates an simple method of extracting cellulose nanofibers (CNF) from cellulose microfibers (CMF) obtained from the plant Stipatenacissima. Here, a method for the production of CNF from CMF extracted from Alfa grass by exfoliation in polyvinyl alcohol (PVA) solution, is demonstrated. The CMF were produced in powder form and exfoliated in PVA aqueous solution to produce composites with 2, 4, 5 and 10?wt-% of CNF. Scanning Electron Microscopy demonstrated exfoliation of CMF, dispersion of the CNF and wetting by the polymer. The composites were characterised by thermogravimetry, differential scanning calorimetry, X-ray diffraction and tensile testing. The addition of CNF to PVA reduced the crystallinity degree of PVA. The large increase of the Young’s modulus from 38 to 113% (relative to pure PVA) for composites with 2 to 10?wt-% of CNF incorporation is consistent with the extensive exfoliation of CMF into CNF and its excellent interface with PVA.     

Effect of the nanoparticles in the stability of hydrolyzed polyacrylamide/resorcinol/formaldehyde gel systems for water shut-off/conformance control applications

The main objective of this work is to evaluate the inclusion of nanoparticles to partially hydrolyzed polyacrylamide/resorcinol/formaldehyde gel systems to improve the stability under static and dynamic conditions. Oxide nanoparticles (<100 mg·L⁻¹) of SiO₂, Al₂O₃, MgO, and Cr₂O₃ were employed and characterized by their physicochemical properties. Gels were prepared and subsequently placed at 70 °C for evaluating the nanoparticles influence in gel strength through rheological properties and syneresis measurements. Al₂O₃ nanoparticles showed the highest potential for the reduction of the syneresis phenomena, followed by MgO and Cr₂O₃. The SiO₂ nanoparticles lead to a higher degradation of the gel. As the zeta potential increases, the syneresis of the gel system decreases. The nanoparticles did not significantly affect the storage modulus, describing similar gel strength than the original gel. Also, displacement tests showed an incremental of 64% of oil recovery regarding the system in the absence of Al₂O₃ nanoparticles. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47568.     

The water state in crosslinked poly(vinyl alcohol)–collagen hydrogel and its swelling behavior

Poly vinyl alcohol (PVA) with pendent carboxyl group was synthesized and verified. The collagen was chemical crosslinked with the produced PVA under the help of crosslinker. Then, the PVA–collagen hydrogels were prepared through the repeated freezing–thawing. Since the water states in hydrogels play an important role in the performance of the product, thermogravimetric (TG) analysis and differential scanning calorimeter (DSC) were conducted to study the different states of water. The results indicated that the weight ratio of nonfreezable water to dry gel in PVA–collagen hydrogels was about 25%. Meanwhile, the swelling behaviors in distilled water and 0.9% saline were studied. The one‐phase exponential associate equation can fit the process very well. Calculated from the simulation equation, the swelling ratios at equilibrium in distilled water and saline were 14.353 g/g dry gel and 14.205 g/g dry gel, respectively. The results illustrated that the ions in solution would decrease the swelling ratio of the hydrogel. At the same time, the lyophilization might have slighter influence to the microstructure of hydrogels and should be more suitable for the swelling research than heat drying. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Water sorption and water binding properties of crosslinked polyacrylamides: effect of macromolecular structure and crosslinking

The water binding properties of crosslinked copolymers of acrylamide with tetraethyleneglycol diacrylate triethyleneglycol dimethacrylate, N,N′-methylene bisacrylamide and divinylbenzene were investigated. It was observed that the freezing water contents of these copolymers depend on nature of the monomers and crosslinkers, as well as on the extent of crosslinking.     

Rheological properties of new polymer compositions for sand consolidation and water shutoff in oil wells

The rheological properties of some newly developed polymer compositions have been investigated with and without crosslinking. These polymer compositions were developed as a water shutoff and sand consolidation treatment agents for producing oil and gas wells. The effects of several variables on the rheology of the compositions were evaluated over a wide range of temperatures (25–110°C), shear rates (0–500 s^?1), brine percentages (0–15%), crosslinker types and concentrations (0–3%), and polymer concentrations (6–50%). It was found that increasing the shear rate from 0 s^?1 to 100 s^?1 caused shear thinning and reduction of the viscosity of the dilute solutions (6–13%) from 25 cP to ～ 3 cP at 80°C. In contrast, for the concentrated solutions (20–50%), the viscosity dropped slightly in the shear rate range 0–10 s^?1, and subsequently decreased more slowly up to shear rates of 500 s^?1. The viscosities of all polymer solutions dropped by a factor of 2 as the brine concentration increased from 0% to 15%. Finally, aging time coupled with shear rates and higher percentages of crosslinkers accelerate the buildup of viscosity and gelation time of the polymer compositions. For concentrated solutions, shear rates ranging within 0–200 s^?1 accelerated gelation time from 9.75 h to 2–3 h, when they were sheared at 80°C. The polymeric solutions exhibited Newtonian, shear‐thinning (pseudo‐plastic), and shear‐thickening (dilatant) behavior, depending on the concentration, shear rate, and other constituents. In most cases, the rheological behavior could be described by the power law. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

The effect of degree of polymerization on the structure and properties of polyvinyl alcohol fibers with high strength and high modulus

Polyvinyl alcohol (PVA) fibers were prepared using PVA with different degree of polymerization (DP) under the same wet spinning process. The effect of the DP of PVA on the structures and properties of PVA and PVA fibers were studied by using nuclear magnetic resonance hydrogen spectroscopy (¹H-NMR), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), differential scanning calorimeter (DSC), thermo gravimetric analysis (TGA), and environmental scanning electron microscope (ESEM). The results showed that DP had little effect on the crystallinity and tacticity of PVA, but had a positive effect on melting temperature, and initial decomposition temperature of PVAs. The hot drawing ratio determined by the spinning process where the PVA fibers could be continuously collected without breaking. The drawing ratio was decreased with an increase of DP, resulting in an increase of the final fiber diameter. The PVA fibers with medium DP and medium size demonstrated high strength and high modulus, but relatively low breaking elongation. It suggested that high DP of PVA was not a guarantee of high strength and high modulus PVA fibers, but rather a primary structure factor. The fiber performance was determined by a comprehensive effect combining a variety of factors including polymer properties and spinning conditions. It provided a guideline for PVA fiber manufacture that the PVAs with different DP require different spinning processes to obtain optimal fiber performance.     

Preparation and characterization of PVA films with magnetic nanoparticles: The effect of particle loading on drug release behavior

This article deals with the drug release behavior of theophylline (Th) from poly(vinyl alcohol) (PVA) hydrogels, prepared with magnetic nanoparticles at different particle loadings. These biocompatible matrices were obtained by incorporating different amounts of an aqueous ferrofluid into PVA hydrogels, loaded with Th as a marker for drug‐delivery studies. PVA films with magnetic particles proved to be magnetic field‐responsive materials as the drug release decreased through the application of a relative low and uniform magnetic field for particle concentrations of 0.9% w/w or higher. Moreover, the percentage of restriction of drug release is found to be correlated with particle loading. The in vitro release profiles were analyzed by applying a semiempirical power law to obtain the kinetic parameters. The value of the release exponent was found to be in the range 0.54–0.56 in all experiments, which thus indicates a predominant diffusional mechanism for drug release from these smart magnetic hydrogels. This effect suggests the possibility of modulating the release behavior by controlling the particle content in the preparation of the composites. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

The oxygen production step of a copper-chlorine thermochemical water decomposition cycle for hydrogen production: Energy and exergy analyses

In the copper-chlorine (Cu-Cl) thermochemical cycle water is decomposed into its constituents (oxygen and hydrogen) by a series of chemical reactions. The cycle involves five steps in which three thermally driven chemical reactions and one electrochemical reaction take place. Oxygen is produced during one of the main chemical reactions. In the present study, the O₂ production step is described with its operational and environmental conditions, and energy and exergy analyses are performed. The cycle is assumed driven using nuclear energy. Various parametric studies are carried out on energetic and exergetic aspects of the step, considering variable reaction and reference-environment temperatures. At a constant reference-environment temperature of 25 °C, the exergy destruction of the O₂ production step varies between 4500 and 23,000 kJ/kmol H₂ when the reaction temperature increases from 450 to 1000 °C. At a 500 °C reaction temperature and a 25 °C reference-environment temperature, the exergy destruction for this step is found to be 5300 kJ/kmol H₂. At a reaction temperature of 500 °C and a reference-environment temperature of 25 °C, the exergy efficiency of the step is determined to be 96% and to decrease with increasing reaction temperature and/or reference-environment temperature.