Thermosensitive hydrogels based on N‐isopropylacrylamide (NIPAAm) and 2‐hydroxyl ethyl acrylate (2‐HEA) were synthesized with different composition ratios at 50:50 and 70:30 mol% using ammonium persulfate as free radical initiation system. The hydrogel was characterized by Fourier transform infrared spectroscopy (FTIR). The interpolymer complex between hydrogels and linear with poly(acrylic acid) (PAA) with different molecular weight was studied. The effect of pH, molecular weights, inorganic salt (NaCl) as well as surfactants concentrations on the complexation was investigated. The swelling behavior of the thermosensitive hydrogels in PAA solutions went up with increasing pH and molecular weight of PAA. However, the decreasing the concentration of surfactants sodium dodecyl sulfate (SDS) and cetylpyridinium bromide (CPB) increased the swelling behavior of hydrogels.
Hydrogel copolymers based on N,N-dimethyl acrylamide (DMA) and acrylic acid (AAc) were synthesized using a solution polymerization technique with different monomer ratios and ammonium persulfate as an initiator. This paper investigates the thermal stability, physical and chemical properties of the hydrogel copolymer. Testing includes Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and elemental analysis (CHNS). The copolymer composition was determined by elemental analysis, and the reactivity ratios of monomers were calculated through linearization methods such as Fineman–Ross (FR), inverted Fineman–Ross (IFR), Kelen–Tudos (KT) and Mayo–Lewis (ML). Good agreement was observed between the results of all four methods. The ratio of r1 and r2 were 0.38 (r1) and 1.45 (r2) (FR), 0.38 (r1) and 1.46 (r2) (IFR), 0.38 (r1) and 1.43 (r2) (KT), and 0.38 (r1) and 1.45 (r2) (ML). Hydrogel copolymers exhibited good thermal stability, and SEM showed three-dimensional porous structures. Antibiotic-free and antibiotic-loaded hydrogels demonstrated antimicrobial properties against both Gram-positive and Gram-negative bacteria. As the ratio of DMA in hydrogel copolymer increased, the activity of copolymer against bacteria enhanced. The results indicated that these hydrogels have the potential to be used as antibacterial materials.
Hydrogel dressings for biomedical application were obtained by γ-irradiation of poly-N-vinipirrolidon (PVP), agar-agar, polyethylene glycol and silver nitrate solution. Influence of irradiation doses (range from 25 kGy to 75 kGy), silver nitrate concentration and PVP concentration in initial monomer mixture on properties of obtained material were investigated. Presence and distribution of silver nanoparticles in obtained bandages is confirmed by optical microscopy and atomic force spectroscopy. Antimicrobial activity study in vitro showed antimicrobial activity, flexibility, high sorption capacity to water and biological fluids.
Physico-mechanical properties of cement pastes were studied by setting time, combined water, compressive strength, SEM as well as porosity in presence of blend polymers. Blend polymers were used based on polyvinyl alcohol and carbamide with blend ratios 20/80, 40/60 and 80/20 respectively. The addition of blend polymers to cement pastes affected the physico-mechanical properties of cement pastes. As the content of carbamide in the polymer blends decreased, the water of consistency decreased, whereas the setting times (initial & final) were elongated. The combined water content and compressive strength of the hardened cement pastes were increased at all ages of hydration. The SEM images showed that the addition of these polymers to cement material improves the dispensability and workability of cement pastes.
In this work, we report the first molecular weight-controlled amphiphilic polybetaine synthesis using various hydrocarbons via reversible addition−fragmentation chain-transfer (RAFT) polymerization. The experimental separation of the alkyl aminocrotonate tautomers, which has been the subject of debate, was completed for the first time. The enamine form of these tautomers was further used as a monomer for the RAFT polymerization of amphiphilic polycarboxybetaines. Self-assembly of the amphiphilic polycarboxybetaines showed micelle structures from spherical, rod-like to fractal in the aqueous media due to the competition between both electrostatic and hydrophobic forces. Hydrophobically dominant interactions among amphiphilic polycarboxybetaines and long-chain hydrocarbon alkane molecules were investigated to understand long-chain hydrocarbon alkane crystallization using alkane crystal deposition and viscosity experiments. Strong hydrophobic forces between poly(hexadecyl-grafted aminocrotonate−methacrylic acid) and long-chain hydrocarbon alkane molecules changed the surface properties of the long-chain hydrocarbon alkane nucleus and inhibited the growth of paraffin crystals.
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