Ratio Of Acrylamide Research Articles

SYNTHESIS OF POLYACRYLAMIDE HYDROGELS WITH PORPHYRIN FRAGMENTS IN THE SIDE CHAIN IN THE PRESENCE OF IMIDAZOLIUM IONIC LIQUIDS

The acrylamide hydrogels containing the porphyrin fragments have been obtained by radical polymerization in a solution. The synthesis has been carried out in the presence of imidazolium ionic liquids with length of the alkyl substituent in the imidazolium ring from C4 to C8. The influence of the used ionic liquids on the structure and some properties of the resulting porphyrin-containing acrylamide hydrogels has been established. The addition of an ionic liquid with a different length of the alkyl substituent into the reaction system can influence the structural changes that occur with the porphyrin comonomer during copolymerization with acrylamide. The formation of bacteriochlorin-like structures is inhibited in the presence of an ionic liquid in the reaction medium. This effect is most noticeable when using an imidazolium ionic liquid with a C8 alkyl substituent length. Hydrogels synthesized in the presence of ionic liquids have lower specific surface area compared to ones obtained without the use of ionic liquids. The lowest specific surface area values were shown by hydrogels synthesized using 1-octyl-3-methylimidazolium bromide. It was also found that the introduction of ionic liquid into the reaction mixture can contribute to both increase and decrease in the numerical values of the sorption characteristics of the resulting hydrogels, depending on the length of the alkyl substituent in the imidazolium ring and a porphyrin : acrylamide ratio. Hydrogels synthesized using 1-hexyl-3-methylimidazolium bromide and 1-octyl-3-methylimidazolium bromide at an initial porphyrin : acrylamide ratio of 1:20 have the highest degree of swelling. Varying the ratio of the initial monomers and the structure of the imidazolium ionic liquid during the copolymerization process allows to control the physicochemical characteristics of the resulting porphyrin-containing hydrogels, which can be useful for solving various applied problems. For citation: Pechnikova N.L., Smirnov A.S., Lyubimtsev A.V., Aleksandriiskiy V.V., Ageeva T.A. Synthesis of polyacrylamide hydrogels with porphyrin fragments in the side chain in the presence of imidazolium ionic liquids. ChemChemTech [Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol.]. 2024. V. 67. N 6. P. 73-79. DOI: 10.6060/ivkkt.20246706.7053.

Reconstructing hepatic metabolic profile and glutathione-mediated metabolic fate of acrylamide

The toxicity of acrylamide (AA) has continuously attracted wide concerns as its extensive presence from both environmental and dietary sources. However, its hepatic metabolic transformation and metabolic fate still remain unclear. This study aims to unravel the metabolic profile and glutathione (GSH) mediated metabolic fate of AA in liver of rats under the dose-dependent exposure. We found that exposure to AA dose-dependently alters the binding of AA and GSH and the generation of mercapturic acid adducts, while liver as a target tissue bears the metabolic transformation of AA via regulating GSH synthesis and consumption pathways, in which glutamine synthase (GSS), cytochrome P450 2E1 (CYP2E1), and glutathione S-transferase P1 (GSTP1) play a key role. In response to high- and low-dose exposures to AA, there were significant differences in liver of rats, including the changes in GSH and cysteine (CYS) activities and the conversion ratio of AA to glycidamide (GA), and liver can affect the transformation of AA by regulating the GSH-mediated metabolic pathway. Low-dose exposure to AA activates GSH synthesis pathway in liver and upregulates GSS activity and CYS content with no change in γ-glutamyl transpeptidase 1 (GGT1) activity. High-dose exposure to AA activates the detoxification pathway of GSH and increases GSH consumption by upregulating GSTP1 activity. In addition, molecular docking results showed that most of the metabolic molecules transformed by AA and GA other than themselves can closely bind to GSTP1, GSS, GGT1, N-acetyltransferase 8, and dimethyl sulfide dehydrogenase 1. The binding of AA-GSH and GA-GSH to GSTP1 and CYP2E1 enzymes determine the tendentiousness between toxicity and detoxification of AA, which exerts a prospective avenue for targeting protective role of hepatic enzymes against in vivo toxicity of AA.

Efficient magnetic flocculation for microalgae harvesting using a novel composite flocculant of Fe3O4-based starch-grafted-cationic polyacrylamide

As a flocculant for algae harvesting, a novel magnetic starch-grafted-cationic polyacrylamide composite (MAG@ST-g-CPAM) was developed in this study, and the harvesting efficiency of the composite was assessed with comparison to starch, Fe3O4 magnetite nanoparticles, cationic polyacrylamide and starch-grafted-cationic polyacrylamide. The feeding ratios for flocculant synthesis were optimized, and impacting factors were examined. Magnetic particles were recovered for cyclic use, and the effect of MAG@ST-g-CPAM flocculation on water reuse was examined. The results showed that MAG@ST-g-CPAM flocculation successfully achieved harvesting efficiencies of 93.2 % and 97.3 % at doses of 25 mg/L and 30 mg/L, respectively, which were superior to those of other flocculants. The optimized feeding ratio of acrylamide:Fe3O4:starch was 6:4:3. The late exponential algal growth solution with a pH range of 5–6 was most favorable for algae flocculation. A total of 93.7 % of Fe3O4 magnetite nanoparticles was recovered at pH = 3, and flocculation facilitated the reuse of water by effectively eliminating fulvic acids from the culture solution. This study demonstrated that MAG@ST-g-CPAM is a promising flocculant for algae harvesting.

Laboratory evaluation of a controllable self-degradable temporary plugging agent in fractured reservoir

In order to solve the uncontrollable swelling ratio and degradation time and insufficient strength of conventional self-degradable temporary plugging agent (CSD-TPA), a controllable self-degradable temporary plugging agent (SD-TPA) was proposed. A series of SD-TPA were prepared with free radical polymerization, and the SD-TPA was synthesized by different mass ratios of acrylamide, acrylic acid, hydrophobic monomer, and modified nanoparticles. The effects of modified nanoparticles content, hydrophobic monomers content, temperature, and salinity on its swelling performance, self-degradable performance, and rheological properties were researched systematically. The plugging and unblocking performance of SD-TPA were studied by a core displacement test. The experimental results showed that SD-TPA can be gelatinization after 4 h at 40 °C. Under the formation condition, SD-TPA had better viscoelasticity, shear resistance, and higher yield stress than CSD-TPA. The core plugging rate increased from 86.44% to 91.41%, and the formation damage rate decreased to 14.11%. This work provides a new temporary plugging material during hydraulic fracturing process and the swelling ratio, degradation time, and insufficient strength of SD-TPA can be adjusted according to the requirement of fracturing.

Impact of composition and salinity on swelling and gel strength of poly (acrylamide-co-acrylic acid) preformed particle gel

The effects of various material compositions and reservoir environments on the ultimate strength and swelling kinetics of a commercial preformed particle gel (PPG) have been investigated. This study used different ratios of acrylamide and acrylic acid copolymers with a specific crosslinker concentration. Results have indicated that increasing the acrylic acid proportion enhances the PPGs’ ability to swell but weakens their network structure. In contrast, increasing the crosslinker content decreases the swelling ratio and increases the gel strength. The highest equilibrium swelling capacity among the six preformed particle gel samples was obtained for PPG2, which has the highest acrylic acid amount and the lowest crosslinker content, with a swelling ratio of 2400 g/g in deionized water and 59.8 g/g in brine 1 (67535.8 mg/l). On the contrary, PPG5, with the lowest acrylic acid and highest crosslinker content, has a swelling capacity of 239 g/g and more than 17 g/g in distilled and brine 1, respectively. Yet, PPG5 has the highest swollen gel strength of 615.5 Pa in deionized water and 3344 Pa in brine 1. The PPGs’ swelling ratios showed stepwise improvements along with increasing temperature, notably after 50 °C, yet, the storage modulus (G′) was negatively affected. The PPGs revealed the highest swelling behavior in pH 6–8, decreasing dramatically in more acidic and basic conditions. The swelling ratios of the PPGs in brine 1 at 50 °C were between 12 and 32 g/g, having strengths in the range of 566–5508 Pa, depending on the crosslinker ratio. The PPGs also demonstrated the ability to compete with other commercial PPGs as they have shown physical and thermal stability when aging at 50 °C, specifically those with high crosslinker content (PPG5).

Synthesis and rheological properties of water soluble ionic copolymers as modifier fluids at high temperature and saline media

AbstractPolymer flooding depicts an interesting strategy to improve the enhanced oil recovery (EOR). This work aims with the synthesis of ionic thermo‐responsive copolymers able to be used as rheological modifiers for EOR under harsh conditions (250,000 ppm of NaCl at 150°C). Copolymers composed of different molar ratio of acrylamide, N‐isopropylacrylamide and 2‐acrylamide‐2‐methyl‐1‐propanesulfonic acid were prepared in aqueous media via free radical polymerization at 50°C using 4,4′‐azobis(‐4″‐cyanopentanoic) acid (ACPA) as initiator. Nuclear magnetic resonance analyses demonstrated the structure and molar composition of synthesized copolymers. Rheological measurements performed at different concentration from 1 to 8 wt% demonstrated an increase in the viscosity from 2000 to 600,000 mPa.s. Aqueous mixtures of polymer at 5 wt% and NaCl at different concentration (5, 10, 15, 20, and 25 wt%) was analyzed. Copolymer ([PAM]/[PNIPAM] = 50/50) displayed a phase separation at 15 wt% of NaCl. Solutions of polymer at 5 and 25 wt% of NaCl were heated at 150°C for 72 h. Results revealed both thermal stability and saline tolerance of copolymers [PAM]/[PNIPAM]/[PAMPS‐Na] = 25/25/50, 35/35/30, and 50/0/50 under harsh conditions with the absence of phase separation of the brine polymer solutions.

High-temperature-operating (over 140 °C) Li-ion supercapacitor via water-locking bimodal cross-linked hydrogel

The utilization of quasi-solid conducting medium possessing superior interfacial properties represents a significant approach in tackling the issue of leakage and stability in supercapacitors. However, preserving the conductivity of ions like Li+ and enabling their adaptability to high-temperature environments pose significant challenges to the improvement of water-locking capacity. Herein, a bimodal cross-linked hydrogel with a mesoporous structure has been developed based on the polyacrylamide-lithium chloride (PAM-LiCl) hydrogel system using polyethylene glycol (PEG). This hydrogel not only exhibits a high water-binding capacity but also facilitates the migration of Li-ions. Using activated carbon as the electrode material, the assembled quasi-solid state supercapacitor devices achieve a single electrode specific capacitance of 32.6 F/g at 0.1 A/g and an energy density of 1.77 W h/kg by varying the ratio of acrylamide and polyethylene glycol (AM/PEG). The findings of this study demonstrate that utilizing a bimodal cross-linked hydrogel can enable the operation of a supercapacitor at high temperatures above 140 °C.

Acrylamide reduction in potato chips as functional food product via application of enzymes, baker's yeast, and green tea powder

Since the discovery of acrylamide in heat-treated foods (crisps and biscuits) in April 2002, by a Swedish study, many efforts have been made to reduce acrylamide levels in foods. Consideration was given to reducing acrylamide levels by reducing Maillard reaction products. However, the production of potato chips creates acrylamide, a carcinogenic compound. This study aimed to use a new quantitative index and formula for l-asparaginase, glucose oxidase, their 1:1 blending enzymes, baker's yeast and green tea powder (0.5 g/kg distilled water) to reduce acrylamide production in potato chips and evaluate the products on some new indicators, such as asparagine reduction (%), acrylamide reduction (%), Asparagine / Acrylamide ratio (AAR) and Asparagine content (mg/kg). The highest acrylamide concentrations were reduced from 1346.0 ± 7.9 mg/kg in the blank sample (control) to 285.7 ± 3.2 and 325.3 ± 10.5 mg/kg in the baker's yeast sample (CT4) and green tea sample (CT5) treated sample, respectively. The potato chips treated with 0.5 g/kg l-asparaginase (CT1) reduced the acrylamide level by approximately 70.65±0.31%, while the CT4 samples showed 78.77±0.21% and asparagine contents of 116.0 ± 5.3 mg/kg and 195.0 ± 5.0 mg/kg, respectively.The results showed that some enzymes, baker's yeast and green tea powder could control the formation of acrylamide, which was formed during the processing of potato chips, allowing the food industry to produce low acrylamide foods from high starch food products such as potatoes. It has the ability to be used as a functional food, as well as to protect the human body of school-age children and adolescents from absorbing 70–80% of their daily acrylamide intake without these treatments.

Intrinsic and Extrinsic Tunability of Double-Network Hydrogel Strength and Lubricity.

Double-network (DN) hydrogels are promising materials for tissue engineering due to their biocompatibility, high strength, and toughness, but understanding of their microstructure-property relationships still remains limited. This work investigates a DN hydrogel comprising a physically crosslinked agarose, as the first network, and a chemically crosslinked copolymer with a varying ratio of acrylamide and acrylic acid, as the second network. The charge, intrinsic to most DN hydrogels, introduces a responsive behavior to chemical and electrical stimuli. The DN strengthens agarose hydrogels, but the strengthening decreases with the swelling ratio resulting from increasing acrylic acid content or reducing salt concentration. Through careful imaging by atomic force microscopy, the heterogenous surface structure and properties arising from the DN are resolved, while the lubrication mechanisms are elucidated by studying the heterogeneous frictional response to extrinsic stimuli. This method reveals the action of the first (agarose) network (forming grain boundaries), copolymer-rich and poor regions (in grains), charge and swelling in providing lubrication. Friction arises from the shear of the polymeric network, whereas hydrodynamic lift and viscoelastic deformation become more significant at higher sliding velocities. We identify the copolymer-rich phase as the main source of the stimulus-responsive behavior. Salt concentration enhances effective charge density and reduces viscoelastic deformation, while electric bias swells the gel and improves lubrication. This work also demonstrates the dynamic control of interfacial properties like hydrogel friction and adhesion, which has implications for other areas of study like soft robotics and tissue replacements.

Facile synthesis of high-entropy zirconate nanopowders and their sintering behaviors

The challenge in synthesizing high-entropy ceramic (HEC) nanopowders is to suppress severe grain coarsening and particle agglomeration, which occur at elevated temperatures. This challenge could be addressed by the polyacrylamide gel method. In this work, single-phase high-entropy (La_0.2Nd_0.2Sm_0.2Gd_0.2Yb_0.2)₂Zr₂O₇ and (La_0.2Nd_0.2Y_0.2Eu_0.2Gd_0.2)₂Zr₂O₇ nanopowders without agglomeration were successfully synthesized using the polyacrylamide gel method for the first time. The results showed that phase composition, particle size, and agglomeration degree of the nanopowders were greatly influenced by the molar ratio of acrylamide (AM)/Zr and calcination temperature. These as-synthesized high-entropy zirconate (HEZ) nanopowders could be sintered into fully dense ceramics at 1500 ℃ for 2 h. These HEZ nanopowders showed a phase transformation from a defect-fluorite phase to a pyrochlore phase with the increase of sintering temperature. Additionally, two-step sintering of these nanopowders was conducted, and the HEZ ceramics with fine grains were prepared. The polyacrylamide gel method is simple and easily operated, which is a facile approach of producing the HEC nanopowders with excellent sinterability.

Synthesis and plugging effect of inverse emulsion polymerization microspheres (OPME) for oil-based drilling fluids

It is difficult to seal oil-based drilling fluids in the large pore and micro-fracture formation, and there are few suitable materials for the oil phase with good sealing ability at present. In order to solve the problem of the lack of sealing ability of oil-based drilling fluids, acrylamide, 2-acrylamido-2-methylpropane sulfonic acid, and acryloyl morpholine were used as monomers, N'N-methylenebisacrylamide was used as a cross-linking agent, Span-80 and Tween-60 were used as emulsifiers, and 2,2′-azobis(2-methylpropionamidine) dihydrochloride was used as an initiator. Polymer microsphere emulsion OPME was synthesized by inverse emulsion polymerization. The structure of polymer microspheres was characterized by infrared spectroscopy, scanning electron microscopy, electron microscopy, H NMR, laser particle size analysis and thermogravimetric analysis. The optimal synthesis conditions were determined by the control variable method: the monomer ratio of acrylamide, 2-acrylamido-2-methylpropane sulfonic acid, and acryloyl morpholine was 45:20:15, the amount of emulsifier was 8%, and the reaction temperature was 55℃. The synthetic polymer microspheres were added to the oil-based drilling fluids to perform filtration and loss plugging at atmospheric pressure and high-temperature and high-pressure, as well as pore and artificial fracture core plugging evaluation. The evaluation results show that the permeability reduction rate of pore core can reach 82%, and that of fracture core can reach 100% by adding polymer microspheres with 3% dosage. Finally, the pressure transmission experiment proves that the addition of polymer microspheres can slow the pressure transmission and filtrate intrusion, and enhance the stability of wellbore. Therefore, polymer microspheres are a micron-level plugging agent with good compatibility and high performance with oil-based drilling fluids, and the 3% dosage can better seal the formation of large pores and micro-fractures, which has a good potential for field application.

Efficient ultralong and color-tunable room-temperature phosphorescence from polyacrylamide platform by introducing sulfanilic acid

Pure organic room-temperature phosphorescent (RTP) materials have evoked increasing attention due to their potential application in many fields. However, the preparation of ultralong and color-tunable RTP materials were still facing challenges. Herein, two facile strategies were applied to construct ultralong RTP materials based on non-covalent and covalent linking of sulfanilic acid (SA) on amorphous polyacrylamide (PAM) framework. The hydrogen bonding in PAM/SA and poly(acrylamide-co-4-acrylamidobenzenesulfonic acid) (PAMABS) can effectively help to suppress non-radiative transition, and induce ultralong RTP emission at ambient condition. The RTP emission intensity and lifetime of PAM/SA can be controlled by the molar ratio of acrylamide to SA. Remarkably, PAMABS shows excitation-dependent color-tunable phosphorescence emission. Due to the destructive effect of water on the system rigidity, PAM/SA and PAMABS both exhibit RTP responsiveness to water and heat stimuli. Furthermore, the convenient preparation and excellent properties enable these new organic RTP materials extremely suitable for anti-counterfeiting and information encryption.

Effect of Poly(acrylamide-acrylic acid) on the Fire Resistance and Anti-Aging Properties of Transparent Flame-Retardant Hydrogel Applied in Fireproof Glass.

Poly(acrylamide-acrylic acid) (P(AM-co-AA)) was synthesized via the copolymerization of acrylamide and acrylic acid and well characterized by Fourier transform infrared spectroscopy. Afterward, the obtained P(AM-co-AA) was blended with flame retardants to prepare transparent flame-retardant hydrogel applied in the fireproof glass. The influence of poly(acrylamide-acrylic acid) on fire resistance and anti-aging properties of the transparent flame-retardant hydrogels were studied by assorted analysis methods. The optical transparency analysis shows that the light transmittance of the transparent flame-retardant hydrogel gradually decreases with the decreasing mass ratio of acrylamide to acrylic acid in P(AM-co-AA). Heat insulation testing shows that the heat insulation performance of fireproof glass applying the transparent flame-retardant hydrogel firstly decreases and then increases with decreasing mass ratio of acrylamide to acrylic acid in P(AM-co-AA). When the mass ratio of acrylamide to acrylic acid is 1:2, the obtained P(AM-co-AA) endows the resulting flame-retardant hydrogel applied in fireproof glass with the lowest light transmittance of 81.3% and lowest backside temperature of 131.4 °C at 60 min among the samples, which is attributed to the formation of a more dense and expanded char to prevent the heat transfer during combustion, as supported by the digital photos of char residues. The results of TG analysis indicate that P(AM-co-AA) imparts high thermal stability to the resulting hydrogels due to the hydrogen bonds between carboxyl and amide groups. The accelerated aging test shows that the transparent flame-retardant hydrogel containing P(AM-co-AA) is less affected by aging conditions. Especially, when the mass ratio of acrylamide to acrylic acid in P(AM-co-AA) is 4:1, the resulting transparent flame-retardant hydrogel shows a light transmittance of 82.9% and backside temperature of 173.1 °C at 60 min after 7 aging cycles, exhibiting the best comprehensive properties among the samples.

Study on the preparation and inhibition mechanism of intumescent nanogel for preventing the spontaneous combustion of coal

A green, halogen-free, efficient, stable, and low-cost intumescent nanogel (ING) was prepared by combining an inorganic nanoparticle flame-retardant system with a chemical intumescent flame-retardant system. Polyacrylamide (PAM) gel was prepared by solution polymerization, then the modified nano-silica (MNS) and intumescent flame retardant were added to the PAM gel successively to prepare the ING. The preparation mechanism was analyzed, and response surface analysis showed that the optimal addition ratio of acrylamide, MNS, and potassium persulfate was 10:0.4:0.07, and the optimal reaction temperature was 75 ℃. The modification of nano-silica and the surface morphology of the composite gel were observed by scanning electron microscopy. In the electron spin resonance experiment, the free radical concentration of 5.70131 × 1017/g of the ING inhibited coal was significantly lower than other coal samples. The content of aliphatic hydrocarbon, aromatic hydrocarbon, and the oxygen-containing functional group in the in situ diffuse reflection Fourier transform infrared spectroscopy experiments all indicated that the ING achieved an excellent inhibition effect. Finally, the inhibition mechanism of the ING was analyzed for its physical, chemical, and composite effects. The PAM gel, MNS, and the intumescent flame retardant system demonstrated a triple inhibition effect, which indicates that ING is an ideal material for preventing the spontaneous combustion of coal.

Construction of Porous Starch-Based Hydrogel via Regulating the Ratio of Amylopectin/Amylose for Enhanced Water-Retention.

The performance of hydrogels prepared with traditional natural starch as raw materials is considerable; the fixed ratio of amylose/amylopectin significantly limits the improvement of hydrogel structure and performance. In this paper, starch hydrogels were prepared by physical blending and chemical grafting, with the aid of ultrasonic heating. The effects of different amylose/amylopectin ratios on the microstructure and water retention properties of starch hydrogels were studied. The results show that an increase in amylopectin content is beneficial to improve the grafting ratio of acrylamide (AM). The interaction between the AM grafted on amylopectin and amylose molecules through hydrogen bonding increases the pores of the gel network and thins the pore walls. When the amylopectin content was 70%, the water absorption (swelling 45.25 times) and water retention performance (16 days water retention rate 44.17%) were optimal. This study provides new insights into the preparation of starch-based hydrogels with excellent physical and chemical properties.

Investigation of Swelling Ratio and Textures Analysis of Acrylamide-Nanocellulose Corncobs Hydrogel

Corncobs have a high level of cellulose hence making it suitable to be used as the main ingredient in making hydrogels. Hydrogel are crosslinked polymers capable of absorbing water hundreds to thousands of times their dry weight, but are insoluble in water due to the three-dimensional structure of the polymer network. Hydrogel can be synthesized using corncobs cellulose and acrylate-acrylamide with chemical crosslinking methods. This study aims to determine the effect of adding corncobs cellulose and acrylate-acrylamide on hydrogel ability to swelling ratio, gel fraction and texture analysis. Nanohydrogel were synthesized by cellulose concentration by 5-25% while acrylamide was varied 10,12 and 16 %. The treatment concentration ratio of nanocellulose solution to acrylamide also showed a significantly different effect at 5% level. The optimum hydrogel synthesis was the treatment of 10 % cellulose ratio and 16% acrylamide ratio which has a swelling ability of 15152.3% (g/g) and gel fraction 56.6%. The increasing the concentration of cellulose caused the hardness value to be higher but the springiness value tends to decrease. Morphology analysis showed the surface of hydrogels that are porous, has lumps and forms a three-dimensional tissue.

A study of Chemical Composition and determination of acrylamide in fried potato chips

This study was designed to investigate the chemical composition and estimation of acrylamide in fresh and fried potato chips for the models under study. This study was conducted at the Food Science Laboratories, college of Agriculture, Tikrit University, Iraq. After selecting the potato class used in this research, deep frying was carried out at different temperatures (100, 130, 150, 170, 180), and the time period for frying was (4) minuets..After the process of deep frying of the samples was completed, several analyzes processes were conducted to determine the causes of the formation of acrylamide and the factors affecting it. Potato samples were analyzed for the chemical composition before and after the frying process of the potato chips. The moisture content was measured by a drying oven, and the protein content was measured by Kjeldahl method, the fat content was measured by the speculate method, sugar and ash. The chemical composition of the fresh potato was found to be 76.3%, 0.2%, 2.7%, 1% and 19.8%). The results of the chemical composition of fried potato chips found that the highest humidity at 100 ° C for 4 minutes was 53.2% and the lowest moisture content was 10.12% at 180 ° C for the same period. The highest fat content was 34.04% at 180 ° C and the lowest fat content was 18.03%. The highest protein was at 130 ° C and 1.50%. The highest ash was at 180 ° C and was 3.11% for 4 minutes. As for sugars, the highest percentage was 51.79% when treated 180 ° C for the same period. As for the estimation of acrylamide in the samples of this study, acrylamide was extracted with water (because it has high water solubility) and alcohol Results showed that the formation of acrylamide in fresh potato chips was 5 mg / kg at a time of 4 minutes. As for the formation of acrylamide in fried potato chips at the same period and at different temperatures was (100, 130, 150, 170, 180 ° C), the highest ratio of acrylamide was 2416 μg / kg at 180 ° C compared to the lowest of 136 μg / Kg at 100 ° C and for the same duration of 4 minutes.

Antibacterial and Anti-Fungal Biological Activities for Acrylonitrile, Acrylamide and 2-Acrylamido-2-Methylpropane Sulphonic Acid Crosslinked Terpolymers.

There is a pressing demand to synthesize polymers that have antibacterial and antifungal properties. The aim of this study was to synthesize a crosslinked hydrophilic terpolymer with acrylamide, acrylonitrile, acrylic acid, acrylamido-2-methylpropane sulphonic acid and ethylene glycol dimethacrylate as a crosslinker. The chemical structure and thermal stability of the prepared cross-linked terpolymers were confirmed by spectroscopic and thermal analyses. Moreover, the swelling experiments were performed to investigate their swelling capacity. Furthermore, the efficiency of the synthesized cross-linked polymer gels was assessed as an antimicrobial agent against Gram-positive, Gram-negative bacteria and fungal strains. The synthesized polymers showed broad inhibition effect, with more antibacterial activity by the AM4 polymer sample containing high percentage of acrylonitrile monomer in the prepared terpolymers (4 mol ratio of acrylic acid: 1 mol ratio of acrylamide: 16 mole ratio of acrylonitrile against Gram negative bacterial strain), while sample M3 terpolymer (1 mol ratio of acrylamide: 1 mole ratio acrylonitrile: 3 mole ratio of acrylamido-2-methylpropane sulphonic acid) showed a promising anti-fungal activity.

Facile and Green Preparation of Superfast Responsive Macroporous Polyacrylamide Hydrogels by Frontal Polymerization of Polymerizable Deep Eutectic Monomers

Polymerizable deep eutectic monomers (DEMs) were prepared by mixing various molar ratios of acrylamide (AM) and choline chloride (ChCl). 1H NMR and Fourier transform infrared confirmed that there w...

One-pot green synthesis of polymeric nanocomposite: Biodegradation studies and application in sorption-degradation of organic pollutants

The research work proposes the synthesis of a nanocomposite hydrogel which is a dual combination of binary interpenetrating network (BIPN) and bismuth ferrite nanoparticles. BIPN synthesized from binary graft copolymer (BGC) used as starting material. The cross-linked network of BGC is interpenetrating the newly synthesized cross-linked network of poly(acrylic acid) and the product is named as BIPN. Binary graft copolymer had been synthesized from grafting of guggul aqueous extract with copolymeric chains of acrylamide (primary monomer) and acrylic acid (secondary monomer) crosslinked by N,N′-methylene bisacrylamide (MBA). The maximum percentage swelling was evaluated for BGC through optimization of various reaction parameters: amount of water, binary ratio of acrylamide to acrylic acid, concentrations of MBA, ammonium persulphate, pH, temperature and time. Considering pre-optimized parameters for BGC synthesis, BIPN formation required optimization of only acrylic acid. Maximum percentage swelling obtained was 1497.79% and 308.15% for BGC and BIPN, respectively. Maximum percentage biodegradation of 90.64% and 82.38% were calculated for BGC and BIPN, respectively using composting method. Degradation efficiency of brilliant blue (BB) and fuchsin basic (FB) dyes was in the order: Nanocomposite ≫ BIPN > BGC. Maximum percentage degradation observed in case of nanocomposite was 94.1% and 99.3% in sunlight for BB and FB, respectively. The interaction of dyes with the nanocomposite involved mainly ionic interactions. The adsorption models Freundlich and Langmuir were applicable to overall adsorption and degradation process of BB and FB, respectively. Maximum adsorption capacities corresponding to minimum concentration i.e. 10 mg L−1 for BB and FB were calculated as 0.409 mg g−1 and 0.439 mg g−1, respectively. Second order and first order kinetics were found to be suitable for BB and FB adsorption-degradation pathways, respectively. Intraparticle diffusion mechanism was favorable to both dyes and adsorption followed three steps. Gas chromatography coupled with mass spectrometric analysis could give the degraded products which was helpful in drawing degradation pathway. The degradation process involved active radical species (O2−., OH.) and they carry out oxidation-reduction reactions on dyes to give decolorized solution containing mineral ions.