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PVDF membrane has strong hydrophobicity and low anti-pollution performance, greatly limiting its practical application. These drawbacks have been successfully overcome by designing and then preparing a membrane with a semi-interpenetrating polymer (semi-IPN) of PVDF/poly(acrylic acid) (PAA) as the membrane matrix, TiO2 nanoparticles as functional components and F127 as pore-forming agent. The semi-IPN was prepared by copolymerizing acrylic acid with N,N methyl acrylamide in the presence of PVDF, and the TiO2 gel nanoparticles were in situ formed in the membrane-forming process. The properties of the composite membrane were significantly affected by the semi-IPN, F127 and TiO2. By adjusting the membrane structure with the semi-IPN, F127 and TiO2 nanoparticles, we prepared a composite membrane with a water contact angle of 40o, a BSA rejection ratio of 87.5% and a water flux of 802.5 L/m2/h/bar. After a simple UV irradiation, the water flux of this composite membrane rose to 1030 L/m2/h/bar, without any rejection decline. The membrane contaminated by humic acid could recover the water flux up to above 95.3% of its original value by a single UV irradiation, showing a very good antifouling performance. In addition, the composite membrane also exhibited a very strong pollution resistance and separation performance for bovine serum albumin and oil-water emulsion. All in all, based on the synergy of the semi-IPN and the evenly dispersed TiO2 nanoparticles, the prepared composite membrane exhibited excellent comprehensive properties and demonstrated a great potential for various separation applications.

The design of heterogeneous catalysts is challenged by the complexity of materials and processes that govern reactivity and by the fact that the number of good catalysts is very small in comparison to the number of possible materials. Here, we show how the subgroup-discovery (SGD) artificial-intelligence approach can be applied to an experimental plus theoretical data set to identify constraints on key physicochemical parameters, the so-called SG rules, which exclusively describe materials and reaction conditions with outstanding catalytic performance. By using high-throughput experimentation, 120 SiO2-supported catalysts containing ruthenium, tungsten, and phosphorus were synthesized and tested in the catalytic oxidation of propylene. As candidate descriptive parameters, the temperature and 10 parameters related to the composition and chemical nature of the catalyst materials, derived from calculated free-atom properties, were offered. The temperature, the phosphorus content, and the composition-weighted electronegativity are identified as key parameters describing high yields toward the value-added oxygenate products acrolein and acrylic acid. The SG rules not only reflect the underlying processes particularly associated with high performance but also guide the design of more complex catalysts containing up to five elements in their composition.

Responsive photonic crystals have attracted much attention due to their strong capability to manipulate the propagation of light in the visible region, but it is still a big challenge to invisibility and mechanical stability. Here, the novel Poly(ether sulfone)/Poly(acrylic acid) inverse opal photonic crystals, which have high mechanical stability and can release visible patterns after wetting with water, are discussed. The Poly(ether sulfone)/Poly(acrylic acid) inverse opal photonic crystals are also responsive to the concentration of ethanol, and the structural color response times increase with increasing ethanol concentration. This design uses the selective infiltration, hydrogen bonding and capillary action of solvent to realize the spectral diversity of reflectance. Owing to the high polarity and hydrogen bonding ability of carboxyl groups, water molecules are adsorbed easily by the poly(acrylic acid) gel. Subsequently, the encrypted information is decrypted due to the redshift of the structural color. Because of its lower polarity and hydrogen bonding ability relative to water, ethanol can impede the absorption of solvent by gel. Therefore, the ethanol concentration can be identified based on the structural color response time. Furthermore, reliable information decryption methods make Poly(ether sulfone)/Poly(acrylic acid) inverse opal photonic crystals potentially uesful as trusted encryption devices.

Multifunctional hydrogels with transparency, ultraviolet (UV)-blocking, stretchable, self-healing, adhesive, antioxidant and antibacterial properties are promising materials for biomedical and relevant applications. However, preparation of these hydrogels at ambient environment without stimuli is still a challenge. Here, a series of hydrogels possessing ultrashort gelation time (~30 s) at room or cold temperature were fabricated based on self-catalytic Fe3+/Tannic acid-cellulose nanofiber (Fe3+/TA-CNF). Fe3+/TA-CNF formed stable redox pairs to activate ammonium persulfate (initiator), generating abundant free radicals to trigger the ultrafast polymerization of acrylic acid (AA). To improve the antibacterial ability of hydrogel, a bilayer hydrogel composite (NF@HG) composed of tetracycline hydrochloride (TH)-loaded electrospun nanofibers and hydrogel layer was fabricated via a mild casting method. The NF@HG exhibited enhanced antibacterial ability and the sustained release of TH can provide long-term antibacterial activity. Besides, cell viability results demonstrated that NF@HG was non-cytotoxic. Taken together, this strategy based on self-catalytic Fe3+/TA-CNF system may inspire new aspects on fast and economical preparation of multifunctional hydrogels or composites, which have attractive industrial applications for biomedical materials.

A site-specific functionalized novel bio-adsorbent (seed composite; MOLL) was used for the remediation of toxic metal ions from the water bodies. The graft co-polymerization using acrylic acid has been carried out onto the polyvinyl alcohol encapsulated seed composite to enrich the bio-adsorbent surface with numerous active carboxylic functionalities responsible for the enhancement in the remediation of cationic metal ions from aqueous system. The morphology, surface area, porosity, presence of functionalities and thermal stability were characterized using SEM-EDX, BET, FTIR and TGA. The functionalized bio-adsorbent (AA-g-PVA-SC-en) exhibited excellent remediation of metals (Pb2+, Cd2+, Cr3+and Ni2+) in the range (90% − 98%) with adsorption capacity (22.44 – 24.73 mg/g). The adsorption capacities in both a single metal and multi-metal system far exceeds from other bio-adsorbents reported so far. The regeneration of functionalized bio-sorbent remained up to six cycles. The findings open up new avenues for the development of a green pre-treatment approach for water remediation, prior to the large scale chemical treatment.

Gel electrolytes based on poly(acrylic acid) and poly(ethylene glycol)diacrylate (PAA-PEGDA-Ca2+) loaded with Ca2+ ions were successfully prepared using gamma irradiation. The use of radiation provides benefits, such as solventless preparation without byproducts. The obtained gel fraction, porosity, and swelling ratio were in the range of 60–90%, 11–60%, and 4–12 g/g, respectively. Fourier transform infrared spectroscopy confirmed the successful crosslinking between PAA and PEGDA. Crystallinity remained unaffected by the incorporation of Ca2+ ions. The thermal decomposition of the gels started at 200°C. The morphology was reported to have a spherical shape. 0.36-0.74 wt.% of Ca2+ was uniformly distributed on the gel electrolyte surface. In the presence of Ca2+ ions, the ionic conductivity of the gels improved by ∼2 times, whereas compressive strength slightly dropped to the range of 6–12 MPa. Graphical abstract Download : Download high-res image (122KB) Download : Download full-size image

A novel CaCO3 nanoparticle modification method by a styrene-acrylic polymer emulsion (SAPE) was introduced. The self-made SAPE was sprayed into the nano-CaCO3 slurry system, and SAPE chains were encapsulated onto the CaCO3 nanoparticle surface. The modified CaCO3 nanoparticle mechanism was discussed. Fourier transform infrared spectroscopy confirmed that the SAPE chain was anchored on the nano-CaCO3 surface by the reaction of the SAPE carboxyl group with the hydroxyl group on the CaCO3. The effect of acrylic acid (AA) amount on the activation degree and oil absorption of CaCO3/SAPE composite nanoparticles was investigated. The amount of AA was 2%, and the activation degree and oil absorption of the product were optimal. The estimated grafting efficiency of the CaCO3/SAPE composite nanoparticles was 90.5% when the amount of acrylamide (AAM) was 1.5%. Scanning electron microscopy showed that the CaCO3 nanoparticles could be dispersed uniformly in polypropylene (PP) film and formed a closed integration by SAPE-modified CaCO3. The styrene-acrylic polymer chains that were grafted on the CaCO3 nanoparticle surface could improve the compatibility between the CaCO3 nanoparticles and PP matrix. The PP composite film with modified CaCO3 nanoparticles had a higher tensile strength than that of pure CaCO3 nanoparticles, which can improve the mechanical properties of the PP material.

To address the rising challenges in self-controlled tandem processes, a catalytic reactor with two reversely-responsive layers was fabricated, for which the two layers acted as the carriers of two different-type active sites so as to achieve the adjustable catalytic ability. This first layer was a shape-memory copolymer consisting of 2-acrylamido-2-methylpropane sulfonic acid and 1-heptene. Given the “frozen” domains in the copolymer at low temperatures, the channel of the substrate became closed. At middle temperatures, the channel of the substrate became open as a result of the activation of the copolymer. The second layer was a copolymer embedding Ag nanoparticles made of polymeric 2-(trifluoromethyl) acrylic acid and 2-vinylpyridine. This layer showed the “closed” channel at low temperatures due to the electrostatic interactions between the two polymeric components, which inhibited the entry of reactants. At higher temperatures, as the polymeric interactions at this layer were broken, the channel in this layer became open for the reactants. In combination with the contained acidic sites and catalytic Ag nanoparticles sites in the two layers, which were individually responsible for catalytic hydrolysis and reduction, the reactor did not show substantive catalytic ability at low temperatures due to the closed channels in both the two layers. At middle temperatures, the reactor ran with simple hydrolysis due to the open channel in the first layer which contained acidic sites. At higher temperatures, the reactor ran with tandem catalytic processes because of the open channels in the two layers. Hence, the design of the dual-responsive catalytic reactor acquired the non-tandem/tandem self-controlled catalytic ability.

Synthesis of polymer nanogels (NGs) for biomedical applications is considered to be a very promising application in radiation engineering. Under high-dose pulse irradiation of dilute aqueous polymer solution, reactive species generated by water radiolysis can create multiple radicals on each macromolecule and consequently induce intramolecular cross-linking of polymer chains, resulting in NG formation. The obtained products are free from harmful monomers, initiators, and cross-linking agents, which makes them potentially applicable for drug delivery applications. One of the biggest challenges in handling and use of nanoparticles, however, is the colloidal stability, when aqueous suspensions are stored for prolonged periods. Therefore, development of the best protocols for the particular nanocarrier storage is key. To address this need, we have performed the prospective study in which we systematically assessed the influence of various processing and storage scenarios feasible in our lab, on the colloidal stability of the radiation-synthesized poly(acrylic acid) (PAA) NG particles in suspension. This allowed us to choose the optimal way of handling the product after its synthesis. We confirmed that none of the strategies we used and tested are substantially detrimental to our product. Filtration with 0.2-μm filters was proven sufficient for sample purification and prolonged storage in aqueous suspension did not exert a negative effect on the colloidal stability of particles suspension. We have also demonstrated that lyoprotectant-free lyophilization was suitable for our polymer nanoparticles. This is an important fact for further application of particles as nanocarriers for biologically active compounds such as targeting ligands or therapeutic moieties.

An aqueous Zn-MnO2 battery with high energy density and good cyclability has been successfully developed with use of an ‘oversaturated gel electrolyte’ (OSGE) prepared by cost-effective acetates and poly(acrylic acid) at 75°C. The electrochemical stability window of the OSGE was extended to 3.45 V at room temperature and was able to maintain this window in temperatures up to 80°C. The ionic conductivity of the OSGE was 3.74 × 10−3 S•cm−1 at room temperature. Molecular dynamics simulation was employed to investigate the contacted cation solvation sheath and could be used to account for the excellent stability of the acetate OSGE. On utilisation of the electrolyte, a high reversibility was demonstrated at room temperature, with 600-hour stripping/plating on Zn metal electrodes and no formation of dendrites. The Zn-MnO2 battery successfully operated for 2000 cycles under an over-charge working voltage (2.0 V). This study not only overcomes the limitation associated with the solubility of salts, but also provides a feasible route for developing a highly stable aqueous Zn-MnO2 battery.

Lumefantrine (LMF), a high-mobility and easy-to-crystallize WHO drug for treating malaria, can form an amorphous salt with poly(acrylic acid) (PAA) that is remarkably stable against crystallization at high humidity and temperature and has fast dissolution rate. The amorphous salt up to 75% drug loading was synthesized under a mild slurry condition easily implemented in basic facilities for global health. Salt formation was confirmed by IR spectroscopy and the much elevated glass transition temperature. At 50% drug loading, the amorphous salt resists crystallization for at least 18 months under the highly stressful condition of 40 °C and 75% RH. In contrast, the dispersion containing neutral LMF in PVP fully crystallized in 4 d and the dispersion in HPMCAS, a weak polyelectrolyte of lower charge density than PAA, crystallized by 50% in 7 d. The amorphous salt at 50% drug loading showed much faster dissolution than crystalline LMF: In SGF, the area under the curve (AUC) was 30 times larger within the gastric emptying time (4 h); in FaSSIF, the enhancement was even larger – by 200 times. Nanodroplets were detected during the dissolution in SGF, possibly accounting for the apparent enhancement of dissolution rate. The LMF-PAA example as a challenging case, along with the previously reported clofazimine-PAA, demonstrates the general utility of amorphous drug–polymer salts to achieve high stability under tropical conditions and enhanced dissolution and bioavailability.

In this study, the impact of particle form of the Cannabis indica plant biofibers and the fiber’s surface tailoring on the physical, thermal, dielectric, and mechanical properties of unsaturated polyester composite specimens manufactured utilizing nonconventional materials were investigated. The mechanical properties such as compressive, flexural, and tensile strengths of the composite specimens were noticed to increase after functionalization of biofiber with acrylic acid and maximum enhancement was found at 20% of biofiber sacking. The physical characterization was concentrated on the assurance of the dielectric constant, dielectric strength, dielectric loss, moisture absorption, chemical resistance, percentage of swelling, limiting oxygen index, and biodegradation of polymer composites under red soil. An increase in dielectric strength from 28 to 29 kV, limiting oxygen index values from 19% to 23%, and moisture/water absorption behavior was noted for resulted bio-composites after surface tailoring of biofiber. To assess the deterioration of the polymeric materials with the temperature, differential scanning calorimetric and the thermogravimetric tests were carried out and enhancement in thermal stability was noted after fortification of polyester composites with functionalized biofiber.

In this research, high-performance epoxy acrylate (EA) coating formulations that contain various acrylate-modified diepoxy siloxane (DESA) intermediates were synthesized and characterized. Firstly, diepoxy siloxane (DES) intermediates, which have varying chain lengths (Mw = 370–3300 Da), were modified by acrylic acid via the ring-opening reaction oxirane group. DESA intermediates were then used in the preparation of ultraviolet (UV)-curable EA formulations. EA was also synthesized via acrylic acid modification of a commercial bisphenol-A-based epoxy resin, used as the standard formulation. EA-based UV-curable formulas were applied on substrates and then cured by UV irradiation for investigating the coating performances. Subsequently, performances of the UV-cured coatings were evaluated by the various test techniques, such as hardness, gloss, cross-cut adhesion force scratch resistance, contact angle, yellowing resistance, abrasion resistance, chemical resistance, and color measurement. The effect of DESA variety on the formations was examined compared to both themselves and the standard formulation. The results showed that the varying amounts and chain lengths of DESA influenced UV-curable coatings’ properties; particularly, the scratch resistance, contact angle, and yellowing resistance significantly enhanced with the increasing chain length of DESA. High-performance UV-curable EA formulations could be produced with the scratch resistance of 4 N, the contact angle of 95°, and high yellowing resistance (ΔE = 0.35).

Effective control of monomer diffusion and reaction rate is the key to achieving a controlled interfacial polymerization (IP) and a high-performance nanofiltration (NF) membrane. Herein, an integration of multirole regulations was synchronously realized using poly(acrylic acid) (PAA) as an active additive in a piperazine (PIP) aqueous phase. Thanks to synergistic interactions, including hydrogen bonding, electrostatic interaction, and covalent bonding between PAA and PIP molecules, together with the increased viscosity of the solution, PIP diffusion was rationally controlled. Moreover, interfacial polycondensation was also restrained via the modestly reduced pH of the aqueous solution. These contribute to the formation of a thinner, looser, more hydrophilic, and higher negatively charged PAA-decorated polyamide selective layer with a unique nanostrand-nodule morphology. The harvested NF-PAA/PIP membrane showed an ∼70% rise in water permeability (up to 23.5 L·m-2·h-1·bar-1) while retaining high Na2SO4 and dye rejections. Furthermore, the optimized NF-PAA/PIP membrane presented a superior fouling resistance capability for typical pollutants, as well as long-term stability during successive filtration. Thus, this work offers a straightforward and impactful approach to regulating IP and promoting NF membrane properties.

This article takes a step forward in understanding the mechanisms involved during the preparation and performance of cross-linked high-drug-loading (HDL) amorphous solid dispersions (ASDs). Specifically, ASDs, having 90 wt % poorly water-soluble drug indomethacin (IND), were prepared via in situ thermal cross-linking of poly(acrylic acid) (PAA) and poly(vinyl alcohol) (PVA) and thoroughly evaluated in terms of physical stability and in vitro supersaturation. Results showed that HDL ASDs having excellent active pharmaceutical ingredient (API) amorphous stability and prolonged in vitro supersaturation were prepared by fine tuning the cross-linking procedure. Unraveling of the processes involved during ASD's formation shed light on the significant role of the cross-linking conditions (i.e., temperature and time), the physicochemical properties of the API, and the hydrolysis level of the cross-linker as key factors in modulating ASD's stability. In-depth analysis of the prepared systems revealed the (1) reduction of API's molecular motions within the cross-linked polymeric networks (through API's strong spatial confinement), (2) the structural changes in the prepared cross-linked matrices (induced by the high API drug loading), and (3) the tuning of the cross-linking density via utilization of low-hydrolyzed PVA as the major mechanisms responsible for ASD's exceptional performance. Complementary analysis by means of molecular dynamics simulations also highlighted the vital role of strong drug-polymer intermolecular interactions evolving among the ASD components. Overall, the impression of the complexity of in situ cross-linked ASDs has been reinforced with the excessive variation of parameters investigated in the current study, offering thus insights up to the submolecular level to lay the groundwork and foundations for the comprehensive assessment of a new emerging class of HDL amorphous API formulations.

PAA/nHAp was synthesized by solvent casting method and characterized by different techniques. nHAp was homogeneously dispersed in nano-sized in PAA matrix. The thermal properties and glass transiti...

In this study, it was investigated experimentally the influence of various solvents (distilled water and ethanol) on the solution properties, spinning performance, and fibre morphology of the electro spun Poly (acrylic acid) nanofibers. Firstly, polymer solutions were prepared at 5 wt % PAA with various solvent ratios of ethanol and distilled water. Then, solution properties such as viscosity, density, pH, conductivity, and surface tension were determined. The production of nanofiber samples was carried out by electrospinning under the optimum process parameters (voltage, distance between electrodes, feed rate, and atmospheric conditions). Finally, the morphological characterization of the nanofiber surface was carried out with SEM. According to the results, it was observed that conductivity, surface tension and the density of the solution increase as the ethanol ratio decreases. On the other hand, pH value increases as the ethanol ratio increases and, so, the acidic value of the solutions decreases. The viscosity increased until the ethanol/distilled water ratio was 50/50 and then decreased as the ethanol percentage decreased to under 50%. In addition, average fibre diameter decreases with ethanol ratio decreases. It is possible to say that solvent type affects solution properties, fibre morphology and spinning performance significantly. Generally, fine, uniform and bead free nanofibers could be electro spun and the PAA solution containing 70 wt % distilled water and 30 wt % ethanol was selected as the optimum in terms of fibre morphology, web quality and spinning performance.

Ionic liquid (IL)-decorated copolymers based on poly((ethylene glycol) methyl ether methacrylate)-co-(acrylic acid)-co-(1-vinyl-3-ethylimidazolium hexafluorophosphate) were prepared and used as bin...

Using N-isopropylacrylamide (NIPAM) and acrylic acid (AAc) as monomers, N,N′-methylenebisacrylamide (MBA) as a cross-linking agent, and molybdenum disulfide (MoS2) as functional particles, a P(NIPAM-co-AAc)/MoS2 composite hydrogel was prepared by free radical polymerization initiated by ultraviolet light. The results of Fourier transform infrared spectroscopy, Raman spectroscopy, and scanning electron microscopy show that MoS2 has been successfully introduced into the P(NIPAM-co-AAc) system, and the obtained composite hydrogel has a porous network structure. Studies on the swelling property and dye adsorption performance show that the addition of MoS2 can increase the swelling ratio of P(NIPAM-co-AAc) hydrogels to a certain extent and can significantly improve the ability of the P(NIPAM-co-AAc) hydrogel to adsorb methylene blue (MB). The adsorption process of MB by the composite hydrogels conforms to the pseudo-second-order kinetics and the Langmuir isotherm adsorption models. The estimated equilibrium adsorption capacity (Qm) using the Langmuir isotherm model can reach 1258 mg/g, mainly due to the electrostatic interaction between the negatively charged groups −COO– and MoS2 particles on the network structure and the positively charged dye MB. The adsorption of MB by P(NIPAM-co-AAc)/MoS2 composite hydrogels depends on the temperature during adsorption. Compared with room temperature, a high temperature of 40 °C above the poly(N-isopropylacrylamide) (PNIPAM) phase transition temperature (∼32 °C) leads to a decreased adsorption capacity of the P(NIPAM-co-AAc)/MoS2 composite hydrogel for MB due to the enhanced hydrophobic properties of the network structure and the decrease of the swelling ratio. The prepared hydrogel material can be used as a good adsorbent for dyes, which is promising in wastewater treatment.

The fast development of Pickering emulsion systems inspires burgeoning demand on the universal synthesis platform for the surface modification of solid particle emulsifiers. In this work, a mild and convenient “visible light–mediated surface grafting through (VSGT)” strategy is proposed. Through the two-step strategy, silica nanoparticles (SNPs) were firstly modified by vinyl alkoxysilane and then used as the substrate for grafting homopolymer brushes via reversible addition-fragmentation chain transfer polymerization under the irradiation of a compact fluorescent lamp (CFL) light source. The whole process was proceeded at room temperature without tedious conditions and complex operations. Importantly, simply by changing the monomer types, hydrophilic acrylic polymer chains can all be grafted on SNP with controlled chain length and relatively uniform high surface densities including poly(acrylic acid) (PAA), poly(N,N-dimethylacrylamide) (PDMA), poly(N-isopropylacrylamide) (PNIPAM), and poly(diacetone acrylamide) (PDAAM). Through the synthesis platform, the interfacial performance of the surface-grafted nanoparticles exhibited as amendable working as Pickering emulsifiers in oil–water system, illustrated by the evolution of interfacial tensions and the inner structures of the corresponding Pickering emulsions. Moreover, the emulsion stabilized by SNP-g-PAA and SNP-g-PNIPAM showed pH and temperature triggered emulsification-demulsification behaviors, respectively, convincing the contribution of the surface grafted polymers and provide a feasible clue for the subtle design on the interfacial texture in advanced Pickering emulsions.

Immobilization of enzymes onto carriers is a rapidly growing research area aimed at increasing the stability, reusability and enzymolysis efficiency of free enzymes. In this work, the role of phase-separation and a pH-responsive “hairy” brush, which greatly affected the topography of porous polymer membrane enzyme reactors (PMER), was explored. The porous polymer membrane was fabricated by phase-separation of poly(styrene-co-maleic anhydride-acrylic acid) and poly(styrene-ethylene glycol). Notably, the topography and pores size of the PMER could be controlled by phase-separation and a pH-responsive “hairy” brush. For evaluating the enzymolysis efficiency of d -amino acid oxidase (DAAO) immobilized carrier (DAAO@PMER), a chiral ligand exchange capillary electrophoresis method was developed with d -methionine as the substrate. The DAAO@PMER showed good reusability and stability after five continuous runs. Notably, comparing with free DAAO in solution, the DAAO@PMER exhibited a 17.7-folds increase in catalytic velocity, which was attributed to its tailorable topography and pH-responsive property. The poly(acrylic acid) moiety of poly(styrene-co-maleic anhydride-acrylic acid) as the pH-responsive “hairy” brush generated topography changing domains upon adjusting the buffer pH, which enable the enzymolysis efficiency of DAAO@PMER to be tuned based upon the well-defined architectures of the PMER. This approach demonstrated that the topographical changes formed by phase-separation and the pH-responsive “hairy” brush indeed made the proposed porous polymer membrane as suitable supports for enzyme immobilization and fitting for enzymolysis applications, achieving high catalytic performance.

Swelling is one of the distinct properties and a significant parameter in the characterization of the crosslinked hydrogels. Swelling investigation at different temperatures was conducted for the produced hydrogel of chitosan grafted acrylamide/acrylic acid. Peleg’s model is a two parameters model, which can be used to describe the absorption of water or swelling. The data show that the swelling degree increases with temperature until it reaches 60°C, after which it decreases as the temperature rises higher. At RT, 30, 40, 60, and 80 °C, the swelling degree values of 1.4, 1.5,1.4, 2.3 and 0.7 g water/g dry hydrogel were observed after 8 hours. The applied models provided a good agreement with the experimental data with high values of the coefficient of determination (𝑅2). The observed F values and the standard error indicate the validity of the proposed model to describe the swelling of hydrogel at different temperatures. The swelling rate and swelling degree can be expressed using a 4th degree polynomial. It was concluded that the exponential association equation model represents swelling characteristics better than the others.

This study aimed to synthesize a silver nanocomposite hydrogel based on poly (acrylic acid) and poly (vinyl pyrrolidone) grafted onto salep biopolymer and its use in controlled drug release. Drug release is one of the medicine goals that have been happening in the different methods, such as injections, pills or sprays. The useful drug dose, has measured by the drug concentration in the blood system, in the specific time. Researches have shown, in above methods, at the first time there is a high concentration of drug in the blood and by passing the time, this concentration decreases, so for achieve the useful drug dose, more drug is needed which it usually causes the increasing of the drug side effects. Thus for preventing these side effects, controlled drug release is investigated in this research. To identify the synthesized hydrogel, Fourier transform infrared spectroscopy (FTIR, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermometric gravimetric analysis (TGA) were used. The results showed that the release of deferasirox from the silver nanocomposite hydrogel network is related to the pH of the environment. In addition, the biodegradability and biocompatibility of this system have led to its use in the pharmaceutical industry.

In this study, a quad acrylic copolymer composed of four monomers namely acrylic acid, methacrylic acid, butyl acrylate, and methyl methacrylate/cloisite30B(C30B) nanocomposites with different load...

Wearable solar radiation sensors based on ionic hydrogels are facilely prepared to simultaneously monitor the radiation dose for the production of vitamin D and the prevention of sunburn. Tetramethylethylenediamine (TEMED) is neutralized with acrylic acid (AA) to obtain tetramethylethylenediamine acrylate (TEMEDA), which is further polymerized with acrylamide by a free radical reaction. By simply adding MB or NR during the polymerization, the final obtained ionic hydrogels can indicate solar radiation. Due to the extent of discoloration, the discoloration speed of MB and NR is correlated to the radiation dose. This wearable sensor can indicate the solar radiation dose required by the human body to synthesize vitamin D through the discoloration of the ionized hydrogel of MB, whereas those with NR are able to illustrate the threshold of radiation dose that causes potential skin hurt. Therefore, the benefit and drawback of solar radiation can be well balanced by optimizing the exposure time to solar irradiation. In addition, polyurethane cross-linked with a thermoresponsive coating is used as band for this wearable sensor. Due to the hydrophilicity below its transition temperature, the cross-linked band possesses the easy cleaning capability of stains after the daily wear. Such type of wearable sensor can be broadly used for monitoring the solar radiation, especially in outdoor activities.

The volume change and shuttle effect of sulfur are detrimental to the stability and electrochemical performance of the sulfur cathode in lithium–sulfur (Li–S) batteries. In this study, a triple cro...

In this manuscript, self-healing nanocomposite hydrogels were successfully fabricated with nanocomposite materials based on functional cellulose nanocrystals (CNCs). CNCs were firstly extracted from microcrystalline cellulose by a typical and eco-friendly method with choline chloride and oxalic acid dihydrate as deep eutectic solvents. Well-defined poly(glycidyl methacrylate) (PGMA) was further grafted on the surface of CNCs by surface-initiated activator generated by electron transfer atom transfer radical polymerization. After ring-opening reaction of PGMA, CNCs@PGMA-OL nanocomposites with diol functional group were successfully obtained and further implanted into poly(acrylic acid)/guar gum-based self-healing hydrogels by multiple reversible weak interactions. These nanocomposite hydrogels display outstanding self-healing and mechanical strength properties, providing a facile strategy for the design and development CNC-based functional materials.

In this research, the MgO nanoparticles were incorporated into (acrylic acid /polyvinyl alcohol) PAA/PVA hydrogel by using gamma radiation technique at a dose rate of 1.9 kGy/k. The unique properties of MgO nanoparticles as structure, active surface properties, and stability make such nanoparticles have considerable potential as antimicrobial agents in food applications. In spite of known antibacterial activity of MgO NPs, the mechanism of metal oxide nanoparticle action on bacteria is complicated and not fully understood. The PAA/PVA system was mixed with various contents of MgO nanoparticles to prepare its MgO nanocomposite hydrogels. The morphology of the PAA/PVA copolymer hydrogels and their MgO nanocomposites hydrogels was characterized by using scanning electron microscopy (SEM) and transmission electron microscopy (TEM) to prove the surface, bulk change, size, and the formation of MgO nanoparticles. TEM measurement estimated that the average particle size of prepared MgO NPs was 7.13 nm. The swelling properties of the various AAc hydrogels and its MgO nanocomposites hydrogels were also studied. The prepared acrylic acid copolymers and their MgO nanocomposites were examined for applicability as antibacterial material, and the results revealed that hydrogels and MgO nanocomposites hydrogels prepared in this study have higher antibacterial activity toward Staphylococus Aureus (S.a.) than Escherichia Coli (E. Coli). The discovery of novel and efficient nanocomposites may have a potential therapeutic role.

Loading and release behavior of a cationic dye, namely, safranine-T, through layer-by-layer (LbL) multilayered films of poly(diallyldimethylammonium chloride) (PDADMAC) and single/blend anionic polyelectrolytes (PEs), namely, poly(acrylic acid) (PAA), and poly(styrenesulfonate) (PSS), are described. The growths of PDADMAC/PSS-PAA multilayers and their safranine-T sorption behavior are monitored using the UV-Vis technique and discussed in terms of blend composition of anionic PEs and pH as well as their hydrophilicity and topography. The dye loading and desorption properties of the LbL films prepared from single/blend negatively charged PEs mainly depend on the interactions of PEs and safranine T. Strong interactions between PSS and safranine T result in a higher dye entrapping inside LbL films whereas either PAA-rich or single PAA-based LbL film exhibits larger dye desorption. A higher PSS content in the feed blend composition leads to an observable increase in theta(ave) and surface roughness whereas the use of PAA can yield a flatter surface due to its partially recomposed chain conformational structure at pH 11. Consequently, LbL multilayers obtained from single and blend polyanions can be considered as an encouraging material platform for the controlled release of charged species such as protein, drug, and dye. because of their tunable physicochemical and morphological properties as well as surface wettability.

Unwanted water production is a serious problem accompanying oil extraction especially in oil-fractured reservoirs. An effective approach to tackle this issue is to utilize gels as a blockage agent. In this paper, an effective series of preformed particle gels (PPGs) was synthesized by a free radical copolymerization of acrylamide and acrylic acid [poly(AAm-co-AA)] copolymers. The key factors of synthesis experiments, gelation time, drying behavior, swelling capacity (in CaCl2·2H2O, MgCl2·6H2O, BaCl2·2H2O, KCl, NaCl, and LiCl saline solutions with 200,000 ppm concentration and pH from 3 to 8), and mechanical and thermal resistance of the synthesized PPGs (with a homemade apparatus) were elucidated. Laboratory results revealed that the prepared PPG sample 1 (9.65 mole ratio of AAm/AA and 6 mol % of MBA) would be a good candidate for controlling water in oil and gas reservoirs with a salinity, pressure, and temperature of up to 200,000 ppm, 300 bar, and 170 °C, respectively, and pH values ranging from 3 up to 8.

Nowadays, hydrogels have been attracted a lot of interest due to their immense potential in different fields such as biomedicine and biotechnology. Biodegradable and biocompatible pH-sensitive chitosan-grafted polyacrylic acid (CTS-g-PAA) hydrogel was synthesized by grafting an acrylic acid monomer onto chitosan at the presence of methylene bisacrylamide as a cross-linking agent and ammonium persulphate as an initiator. FT-IR spectroscopy and scanning electron microscopy (SEM) were used to analyze the properties of the obtained hydrogel. The synthesized hydrogel is suitable for the delivery of many hydrophilic drugs or species. Using a multi-walled carbon nanotube modified-glassy carbon electrode (CNT-GCE), the loading and release conditions of Nile Blue (NB) as an electroactive compound were evaluated utilizing the differential pulse voltammetry (DPV) and cyclic voltammetry (CV). The effect of various parameters on the electrochemical signal of NB was investigated, and the optimal conditions for the efficient performance of hydrogel to delivery of NB were obtained. The electrocatalytic current values show linear dependence to NB concentration in the range of 0.098 – 0.971 μM while the detection limit of this electrochemical platform was 12.3 nM. The unique proposed hydrogel with the electroactive NB has a broad range of possible applications in biosensors for signal enhancement and bioanalysis. Supplementary Information The online version contains supplementary material available at 10.1007/s10854-021-06939-7.

Interaction of the anionic copolymer of acrylic acid and acrylamide with a molar ratio of monomer units of 75 : 25 and poly(N,N′-diallyl-N,N′-dimethylammonium chloride) in aqueous solution is studied. The interaction is accompanied by the formation of a polycomplex stabilized by multiple salt bonds between oppositely charged groups of both polyelectrolytes. A nonstoichiometric polycomplex with a tenfold excess of anionic groups is present in solution in the form of particles with a diameter of about 300 nm; the particles retain their aggregate stability for 30 days. The application of aqueous solutions of individual polymers and the nonstoichiometric polycomplex on the surface of sand with a particle size of 0.15 ± 0.05 mm is associated with the formation of composite polymer-sand coatings. The highest mechanical strength is possessed by coatings with the participation of an anionic copolymer and a polycomplex. For sand and polycomplex coatings, the weight loss during water treatment is 10%, which is lower than that in the case of traditional polyacrylamide soil stabilizer. The polycomplex at a concentration of up to 0.33 wt % does not exhibit toxicity to microorganisms, thereby indicating that the use of a negatively charged polycomplex is promising for obtaining waterproof protective coatings on the surface of sandy soils.

The interaction between the aggregation-induced emissive (AIE) luminogens (AIEgen) and the polymer is the key scientific question in the design of functional AIE hydrogels. In this study, we report the AIE behavior of a poly(acrylic acid) (PAAc) and poly(acrylamide) (PAAm) interpenetrating network (IPN) hydrogel doped with tetra-cationic tetraphenylethene (TCTPE). The cationic AIEgen can bind with PAAc through ionic interaction, while PAAc and PAAm chains can associate with each other through hydrogen-bonds (H-bonds). These two interactions can restrict the intramolecular rotation and thus activate the luminescence of the AIEgen. The PAAc-PAAm H-bonds can be broken by increasing temperature or pH, restoring the intramolecular rotation of the AIEgen and quenching the fluorescence of the hydrogel. Therefore, the TCTPE-doped IPN hydrogel is designed as temperature- and pH-sensitive displayers which can record information imprinted by photo-printing or iono-printing with good switchability and reversibility. Another application of this TCTPE-doped hydrogel is demonstrated as a luminescent soft actuator, which has fast shape deformation and editable fluorescence pattern. The above results reveal a pathway to tune the emission behavior through tuning polymer-polymer and polymer-AIEgen interactions, which may inspire new design strategies of aggregation-induced emissive polymers and broaden their applications.

Grafting by pre-irradiation technique is rarely reported in recent literature. In this respect, natural rubber latex (NRL) films and its blends with potato starch (NRL/P.St) were prepared at various compositions using solution casting technique. Pre-irradiated NRL films with gamma radiation at doses from 30 to 100 kGy were grafted with hydrophilic monomers namely, acrylic acid (AAc) and acrylamide (AAm) to enhance NRL hydrophilicity. The grafted films of NRL and NRL/P.St blends were structurally and morphologically characterized by different techniques including FTIR spectroscopy and scanning electron microscopy (SEM). Hydrophilicity properties of grafted films were studied intensively through evaluating water absorption percentage of the grafted films. The water absorption study concluded that NRL and NRL/P.St blend films grafted with acrylamide have higher water affinity than those grafted with acrylic acid monomer. Enhancing the hydrophilicity of NRL and NRL/P.St blend films make it possible to study the biodegradability of the prepared films. Studying the effect of incubation time in soil on the weight loss of samples showed that the biodegradability of NRL-g-AAm and NRL/P.St (70/30)-g-AAm is higher than their counterparts grafted with AAc. The results showed that the microbial activity inside the specimens in the case of grafted NRL films with AAm monomer was accelerated in the first 10 days in soil burial test. Calculation of the weight loss and digital photographs of the films showed significant differences after 90 days of incubation in soil and the films grafted with AAm have higher weight loss than those grafted with AAc.

The aim of the current research work was to fabricate polymeric nexus for controlled delivery of metoprolol tartrate by using free radical polymerization. Polymer (aloe vera, sodium carboxymethyl cellulose, and meggletose) was crosslinked with monomer (acrylic acid) by using N,N methylene bisacrylamide. Swelling behavior was studied in pH 1.2 and 7.4. Sol gel fraction depicted gel fraction increased with the increase in feed ratio (polymer, monomer, and crosslinker). Optimized formulation was evaluated via Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). FTIR confirmed compatibility of metoprolol with formulated system. Moreover, pH-dependent swelling was observed, experiencing significant swelling at higher pH. SEM depicted porous architecture which is responsible for swelling, drug loading, and release. Dissolution studies showed percentage drug release was significant in pH 7.4. Hence, the current research work demonstrates sustained delivery of metoprolol by employing varying concentration of polymer, monomer, and crosslinker. These fascinating properties made hydrogel a promising carrier for sustained drug delivery.

This study focuses on the synthesis of poly(e-caprolactone) diacrylate (PCLDA) for the fabrication of micelle-cross-linked sodium AMPS wound dressing hydrogels. The novel synthetic approach of PCLDA is functionalizing a PCL diol with acrylic acid. The influences of varying the PCL diol/AA molar ratio and temperature on the suitable conditions for the synthesis of PCLDA are discussed. The hydrogel was synthesized through micellar copolymerization of sodium 2-acrylamido-2-methylpropane sulfonate (Na-AMPS) as a basic monomer and PCLDA as a hydrophobic association monomer. In this study, an attempt was made to develop new hydrogel wound dressings meant for the release of antibacterial drugs (ciprofloxacin and silver sulfadiazine). The chemical structures, morphology, porosity, and water interaction of the hydrogels were characterized. The hydrogels' swelling ratio and water vapor transmission rate (WVTR) showed a high swelling capacity (4688-10753%) and good WVTR (approximately 2000 g·m-2·day-1), which can be controlled through variation of the PCLDA concentration. The mechanical property results confirmed that PCLDA improved the mechanical properties of the hydrogel; the stress increased from 37 to 68 kPa, and the strain increased from 198 to 360% with increasing PCLDA (0-30% wt of Na-AMPS). These hydrogels presented no cytotoxicity based on over 70% cell viability responses (L929 fibroblasts) using an in vitro 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Additionally, the drug release mechanism, kinetic models, and antibacterial activity were determined. The results demonstrated that antibiotics were released from the hydrogel with a Fickian diffusion mechanism and antibacterial activity against Gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa) and Gram-positive bacteria (Staphylococcus aureus). Based on the results obtained, and bearing in mind that further progress still needs to be made, the fabricated hydrogels show considerable potential for meeting the stringent property requirements of hydrogel wound dressings.

Defect passivation is a key strategy to prepare high-performance perovskite solar cells (PVSCs). Even though abundant passivation molecules have been applied, the absence of detailed researches with regard to different functional groups in polymer additives may inevitably impede the establishment of passivation molecules selection rules. In this work, three passivation molecules including poly(vinyl alcohol) (PVA), polymethyl acrylate (PMA), and poly(acrylic acid) (PAA) are employed to systematically analyze the passivation effect from hydroxyl, carbonyl, and carboxyl groups. In general, PVA (-OH) can form hydrogen bonds with perovskite and PMA (-C═O) can complex with uncoordinated Pb2+. Specifically, PAA (-COOH) can interact selectively with MA+ and I- ions via hydrogen bonding and complex with uncoordinated Pb2+ to passivate defects more effectively. Hence, the PAA-incorporated PVSCs based on MAPbI3 achieve the champion power conversion efficiency (PCE) of 20.29% with open-circuit voltage up to 1.13 V. In addition, PAA cross-linking perovskite grains can relieve mechanical stress, as well as occupy the major channels to suppress ion migration and water/oxygen erosion. The corresponding unencapsulated devices demonstrate a superior light soaking stability, retaining more than 80% of the original PCE under one sun illumination for 1000 h.

The absorption process in acrylic acid production was water-intensive. The concentration of acrylic acid before distillation process was low, which induced to large amount of wastewater and enormous energy consumption. In this work, a new method was proposed to concentrate the side stream of absorption column and thus increase the concentration in bottom product by electrodialysis. The influence of operating conditions on concentration rate and specific energy consumption were investigated by a laboratory-scale device. When the voltage drop was 1 V·cP−1 (1 cP=10−3 Pa⋅S), flow velocity was 3 cm·s−1 and the temperature was 35 °C, the concentration rates of acrylic acid and acetic acid could be 203.3% and 156.6% in the continual-ED process. Based on the experimental data, the absorption process combined with ED was simulated, in which the diluted solution from ED process was used as spray water and the concentrated solution was feed back to the absorption column. The results shown that the flow rate of spray water was decreased by 37.1%, and the acrylic acid concentration at the bottom of the tower was increased by 4.56%. The ions exchange membranes before and after use 1200 h were tested by membrane surface morphology (scanning electron microscope), membrane chemical groups (infrared spectra), ion exchange capacity, and membrane area resistance, which indicated the membrane were stable in the acid system. This method provides new method for energy conservation and emission reduction in the traditional chemical industry.