Search Results (10)

Significant progress has been achieved in the development of superabsorbent polymers (SAPs), focusing on enhancing their performance and expanding their applications. Efforts are particularly directed at increasing water absorbency while promoting environmental sustainability. Biodegradable materials such as starch and potassium humate have been successfully integrated with SAPs for desert greening, improving water retention, salt resistance, and seedling survival. The inclusion of nutrient-rich organic-inorganic composites further enhances the durability, efficiency, and recyclability of SAPs. In drought mitigation, polymeric absorbent resins such as polyacrylamide and starch-grafted acrylates have shown efficacy in ameliorating soil conditions and fostering plant growth. In arid environments, agents enriched with humic acid and bentonite contribute to improved soil aeration and water retention, creating optimal conditions for plant establishment. Additionally, the adoption of innovative waste management solutions has led to the production of amphiphilic SAPs from residual sludge, effectively addressing soil nutrient deficiencies and environmental pollution. In the food industry, SAPs containing protease, tea polyphenols, and chitosan exhibit potential for enhancing the stability and quality of seafood products. These advancements highlight the growing relevance of structural optimization approaches in SAP development across diverse applications and underline the importance of continued innovation in these fields. As novel materials emerge and environmental challenges intensify, the potential applications of SAPs are anticipated to expand significantly. Full article

Polymer flooding has achieved considerable success in medium–high permeability reservoirs. However, when it comes to low-permeability reservoirs, polymer flooding suffers from poor injectivity due to the large molecular size of the commonly used high-molecular-weight (high-MW) partially hydrolyzed polyacrylamides (HPAM). Herein, an amphiphilic polymer (LMWAP) with a low MW (3.9 × 10⁶ g/mol) was synthesized by introducing an amphiphilic monomer (Allyl-OP-10) and a chain transfer agent into the polymerization reaction. Despite the low MW, LMWAP exhibited better thickening capability in brine than its counterparts HPAM-1800 (MW = 1.8 × 10⁷ g/mol) and HPAM-800 (MW = 8 × 10⁶ g/mol) due to the intermolecular hydrophobic association. LMWAP also exhibited more significant shear-thinning behavior and stronger elasticity than the two counterparts. Furthermore, LMWAP possesses favorable oil–water interfacial activity due to its amphiphilicity. The oil–water interfacial tension (IFT) could be reduced to 0.88 mN/m and oil-in-water (O/W) emulsions could be formed under the effect of LMWAP. In addition, the reversible hydrophobic association endows the molecular chains of LMWAP with dynamic association–disassociation transition ability. Therefore, despite the similar hydrodynamic sizes in brine, LMWAP exhibited favorable injectivity under low-permeability conditions, while the counterpart HPAM-1800 led to fatal plugging. Furthermore, LMWAP could enhance oil recovery up to 21.5%, while the counterpart HPAM-800 could only enhance oil recovery by up to 11.5%, which could be attributed to the favorable interfacial activity of LMWAP. Full article

A novel hyperbranched polymer with polyacrylamide side chains (HAPAM) was synthesized by aqueous solution polymerization using acrylic acid, acrylamide, 2-acrylamido-2-methyl-1-propanesulfonic acid, hydrophobic monomer of dimethyl octadecyl ammonium chloride, and the homemade skeleton monomer of modified-M_2.0 as raw materials and (NH₄)₂S₂O₈-NaHSO₃ as initiator. The molecular structure, functional groups, and surface morphology of HAPAM were characterized by Fourier transform infrared spectroscopy, nuclear magnetic resonance hydrogen spectroscopy, and scanning electron microscopy. It was found that the performance of HAPAM solution was higher than that of ordinary polyacrylamide solution in terms of thickening ability, shearing resistance, thermal endurance, salt-resistance, resistance-coefficient and residual-resistance-coefficient, ability to reduce interfacial tension between polymer solution and crude oil, and oil-displacement-efficiency. In particular, the enhanced oil recovery of the HAPAM solution was 13.03%, and the improvement of shearing resistance and immunity to chromatographic separation were simultaneously achieved by the HAPAM solution. These results indicate that the successful synthesis of the novel HAPAM opens a promising strategy for developing new high-performance oil-displacing polymers. Full article

The continuous growth in global energy and chemical raw material demand has drawn significant attention to the development of heavy oil resources. A primary challenge in heavy oil extraction lies in reducing crude oil viscosity. Alkali–surfactant–polymer (ASP) flooding technology has emerged as an effective method for enhancing heavy oil recovery. However, the chromatographic separation of chemical agents presents a formidable obstacle in heavy oil extraction. To address this challenge, we utilized a free radical polymerization method, employing acrylamide, 2-acrylamido-2-methylpropane sulfonic acid, lauryl acrylate, and benzyl acrylate as raw materials. This approach led to the synthesis of a multifunctional amphiphilic polymer known as PAALB, which we applied to the extraction of heavy oil. The structure of PAALB was meticulously characterized using techniques such as infrared spectroscopy and Nuclear Magnetic Resonance Spectroscopy. To assess the effectiveness of PAALB in reducing heavy oil viscosity and enhancing oil recovery, we conducted a series of tests, including contact angle measurements, interfacial tension assessments, self-emulsification experiments, critical association concentration tests, and sand-packed tube flooding experiments. The research findings indicate that PAALB can reduce oil–water displacement, reduce heavy oil viscosity, and improve swept volume upon injection into the formation. A solution of 5000 mg/L PAALB reduced the contact angle of water droplets on the core surface from 106.55° to 34.95°, shifting the core surface from oil-wet to water-wet, thereby enabling oil–water displacement. Moreover, A solution of 10,000 mg/L PAALB reduced the oil–water interfacial tension to 3.32 × 10⁻⁴ mN/m, reaching an ultra-low interfacial tension level, thereby inducing spontaneous emulsification of heavy oil within the formation. Under the condition of an oil–water ratio of 7:3, a solution of 10,000 mg/L PAALB can reduce the viscosity of heavy oil from 14,315 mPa·s to 201 mPa·s via the glass bottle inversion method, with a viscosity reduction rate of 98.60%. In sand-packed tube flooding experiments, under the injection volume of 1.5 PV, PAALB increased the recovery rate by 25.63% compared to traditional hydrolyzed polyacrylamide (HPAM) polymer. The insights derived from this research on amphiphilic polymers hold significant reference value for the development and optimization of chemical flooding strategies aimed at enhancing heavy oil recovery. Full article

The article summarizes multivariate field trials of gel-forming soil conditioners for agriculture and urban landscaping in various climatic conditions from arid (O.A.E., Uzbekistan) to humid (Moscow region, Russia). The field test program included environmental monitoring of weather data, temperature, water–air regimes, salinity, alkalinity, and biological activity of various soils (sandy and loamy sandy Arenosols, Retisols, loamy Serozems), productivity and yield of plants (lawns, vegetables) and their quality, including pathogen infestation. The evolutionary line of polymer superabsorbents from radiation-crosslinked polyacrylamide (1995) to the patented “Aquapastus” material (2014–2020) with amphiphilic fillers and biocidal additives demonstrated not only success, but also the main problems of using hydrogels in soils (biodegradation, osmotic collapse, etc.), as well as their technological solutions. Along with innovative materials, our know-how consisted in the intelligent soil design of capillary barriers for water accumulation and antipathogenic and antielectrolyte protection of the rhizosphere. Gel-forming polymer conditioners and new technologies of their application increase the productivity of plant crops and the quality of biomass by 30–50%, with a 1.3–2-fold saving of water resources and reliable protection of the topsoil from pathogens and secondary salinization. The results can be useful to a wide range of specialists from chemical technologists to agronomists and landscapers. Full article

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)/polycaprolactone (PHBV/PCL) polymer mixtures reinforced by cellulose nanocrystals (CNCs) have been obtained. To improve the CNC compatibility with the hydrophobic PHBV/PCL matrix, the CNC surface was modified by amphiphilic polymers, i.e., polyvinylpyrrolidone (PVP) and polyacrylamide (PAM). The polymer composites were characterized by FTIR, DSC, TG, XRD, microscopy, BET surface area, and tensile testing. The morphological, sorption, thermal, and mechanical properties of the obtained composites have been studied. It was found out that with an increase in the CNC content in the composites, the porosity of the films increased, which was reflected in an increase in their specific surface areas and water sorption. An analysis of the IR spectra confirms that hydrogen bonds can be formed between the CNC hydroxyl- and the –CO– groups of PCL and PHBV. The thermal decomposition of CNC in the PHBV/PCL/CNC composites starts at a much higher temperature than the decomposition of pure CNC. It was revealed that CNCs can either induce crystallization and the polymer crystallite growth or act as a compatibilizer of a mixture of the polymers causing their amorphization. The CNC addition significantly reduces the elongation and strength of the composites, but changes Young’s modulus insignificantly, i.e., the mechanical properties of the composites are retained under conditions of small linear deformations. A molecular-dynamics simulation of several systems, starting from simplest binary (solvent-polymer) and finishing with multi-component (CNC—polymer mixture—solvent) systems, has been made. It is concluded that the surface modification of CNCs with amphiphilic polymers makes it possible to obtain the CNC composites with hydrophobic polymer matrices. Full article

The development of techniques capable of using membrane proteins in a surfactant-free aqueous buffer is an attractive research area, and it should be elucidated for various membrane protein studies. To this end, we examined a method using new solubilization surfactants that do not detach from membrane protein surfaces once bound. The designed solubilization surfactants, DKDKC₁₂K-PA_n (n = 5, 7, and 18), consist of two parts: one is the lipopeptide-based solubilization surfactant part, DKDKC₁₂K, fand the other is the covalently connected linear polyacrylamide (PA) chain with different M_w values of 5, 7, or 18 kDa. Intermolecular interactions between the PA chains in DKDKC₁₂K-PA_n concentrated on the surfaces of membrane proteins via amphiphilic binding of the DKDKC₁₂K part to the integral membrane domain was observed. Therefore, DKDKC₁₂K-PA_n (n = 5, 7, and 18) could maintain a bound state even after removal of the unbound by ultrafiltration or gel-filtration chromatography. We used photosystem I (PSI) from Thermosynecoccus vulcanus as a representative to assess the impacts of new surfactants on the solubilized membrane protein structure and functions. Based on the maintenance of unique photophysical properties of PSI, we evaluated the ability of DKDKC₁₂K-PA_n (n = 5, 7, and 18) as a new solubilization surfactant. Full article

Although stimuli-responsive release systems have attracted great attention in medical applications, there has been no attempt at “precise” deep profile control based on such systems, which is greatly need to improve oil recovery. With this in mind, we provided a facile and simple strategy to prepare stimuli-responsive composite capsules of amphiphilic dendrimers–poly(styrene sulfonic acid) sodium/halloysite nanotubes (HNTs) via layer-by-layer (LbL) self-assembly technique, controlling the release crosslinking agent methenamine under different pH or salinity conditions. The release time of methenamine encapsulated in multilayer shells is about 40 h, which can be prolonged with the introduction of salt or shortened via the addition of acid, which accordingly induces the gelation of polyacrylamide (PAM) solutions, taking from a few hours to a dozen days. This study provided a novel approach for controllable release of chemical agents and controllable crosslinking of deep profiles in many application fields. Full article

Delayed crosslinking polymer gel systems are widely utilized in deep profile control processes for water production control in oilfields. In this paper, a kind of delayed crosslinking amphiphilic polymer gel system with adjustable gelation time based on competitive inclusion was prepared and its delayed crosslinking gelling properties were studied. The amphiphilic polymer of P(acrylamide (AM)–sodium acrylate (NaA)–N-dodecylacrylamide (DDAM)) was synthesized and it showed much better salt resistance, temperature resistance, and shear resistance performance compared with hydrolyzed polyacrylamide (HPAM). Phenol can be controlled released from the the cavity of β-cyclodextrin (β-CD) ring in the presence of the hydrophobic group used as the competitive inclusion agent in the amphiphilic polymer backbone. Accordingly, the gelation time of the delayed crosslinking amphiphilic polymer gel system is closely related to release rate of the crosslinker from the the cavity of β-CD ring. This study screened an amphiphilic polymer with good salt resistance and temperature resistance performance, which can be used in high temperature and high salinity reservoirs, and provided a feasible way to control the gelation time of the polymer gel system by the competitive inclusion method. Full article

This work first reports the preparation of super-amphiphilic silica-nanogel composites to reduce the contact angle of water to increase the diffusion of pollutant into adsorbents. In this respect, the silica nanoparticles were encapsulated into nanogels based on ionic and nonionic polyacrylamides by dispersion polymerization technique. The morphologies and the dispersion stability of nanogel composites were investigated to clarify the ability of silica-nanogel composites to adsorb at different interfaces. The feasibility of silica polyacrylamide nanogel composites to act as a high-performance adsorbent for removal of methylene blue (MB) dye and heavy metals (Co²⁺ and Ni²⁺) from aqueous solution was investigated. The surface tension, contact angle, average pore size, and zeta potential of the silica-nanogel composites have been evaluated. The MB dye and heavy metal adsorption capacity achieved Q_max = 438–387 mg/g which is considerably high. The adsorption capacity results are explained from the changes in the morphology of the silica surfaces as recorded from scanning electron microscopy (SEM). Full article