Ratio Of Acrylamide Research Articles

Preparation and characterization of hemicellulosic derivatives containing carbamoylethyl and carboxyethyl groups

A series of novel water-soluble hemicellulosic derivatives, containing carbamoylethyl and carboxyethyl groups, were heterogeneously synthesized from wheat-straw hemicelluloses with acrylamide (AA) under alkaline conditions. The factors such as reaction temperature, reaction time, molar ratio of catalysis to xylose unit in hemicelluloses and molar ratio of acrylamide to xylose unit in hemicelluloses, were investigated. The average degree of substitution (DS) was calculated by 1H NMR spectroscopy. DS values up to 0.23 in a one-step synthesis of hemicelluloses derivatives were obtained. Under optimum conditions (60 °C, NaOH to xylose unit in hemicelluloses molar ratio of 0.8, AA to xylose unit in hemicelluloses molar ratio of 8.0, reaction time of 1 h) an expected ratio of carbamoylethyl group to carboxyethyl group of 4.8 in the hemicellulosic derivatives was obtained. The structural features of the hemicellulosic derivatives were characterized by FTIR, NMR spectroscopy, and by elemental analysis. The current work provides a facile method for the synthesis of hemicellulose derivatives with bifunctional groups, which could be used as wet-end additives in the papermaking industry.

Poly(acrylamide‐co‐acrylic acid)/Poly(vinyl pyrrolidone) Polymer Blends Prepared by Dispersion Polymerization

The structure and properties of a three‐component system, a poly(acrylamide‐co‐acrylic acid)/poly(vinyl pyrrolidone) [P(AM‐co‐AA)/PVP] polymer blend prepared by dispersion polymerization, were studied. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images showed that the resulting P(AM‐co‐AA) microspheres with diameters between 200–300 nm were well‐dispersed in the PVP matrix. Fourier transform infrared spectra (FTIR) showed that intermolecular hydrogen bonding interaction occurred between the dispersed phase and the continuous phase. The mechanical properties of P(AM‐co‐AA)/PVP polymer blends were also determined. With different mass ratios of acrylamide to acrylic acid, it was found that the blends had better mechanical properties with increased AA content.

Effect of Modification of SeO2/Acrylamide Ratios on Diffraction Efficiencies in PVA/AA Photopolymer Films

The highest diffraction efficiency(DE) value after illumination and post-curing of photopolymer films were obtained at the <TEX>$SeO_2$</TEX>/Acrylamide(AA) Ratios of AA 3.0 g, <TEX>$SeO_2$</TEX> 1.0g and the DE's were stable values of over 90%. By the addition of <TEX>$SeO_2$</TEX>, the maximum DE at the initial stage of illumination was reached at 300 seconds, which suggests <TEX>$SeO_2$</TEX> slows down the photopolymerization of AA, which enhances the maximum DE value by giving more migration time. DE variation curve for the optimum composition during extended-time illumination of 9,000 seconds resembles a sine curve due to the combination of the monomer diffusion and the photopolymerization, and the photopolymer film expanded by about 8% after photopolymerization due to monomer migration.

Effect of Modification of SeO2/Acrylamide Ratios on Diffraction Efficiencies in PVA/AA Photopolymer Films

Effect of Modification of SeO₂/Acrylamide Ratios on Diffraction Efficiencies in PVA/AA Photopolymer Films

Homogenous modification of cellulose with acrylamide in NaOH/urea aqueous solutions

A series of cellulose polyelectrolytes, containing acylamino and carboxyl groups, were homogenously synthesized from cellulose with acrylamide in NaOH/urea aqueous solutions. The structure and solution properties of the polyelectrolytes were characterized with elemental analysis, FTIR, NMR, viscometer and zeta-potential measurement. The nitrogen content and total degree of substituent (DS) of the derivatives increased with increasing of the molar ratio of acrylamide to the anhydroglucose unit (AGU) and the cellulose concentration. The DS of carboxyl groups hardly changed because of the similar reaction and hydrolysis conditions, while the DS of acylamino groups increased with increasing of the total DS values of the products. The polyelectrolytes are soluble in water at a total DS as low as 0.36, and the zeta-potential values in pure water are in the range of −15 to −25 mV. The [ η] values of the polyelectrolytes in NaCl aqueous solutions increased apparently with an increase of the pH value in the lower pH region, and reached the maximum value at the pH range from 5 to 6, and while hardly changed at the pH range from 7 to 12. This work provided a facile method for the synthesis of cellulose polyelectrolytes with two different functional groups.

Characterization of hydrogels prepared by the γ irradiation of aqueous solutions of acrylamide and N‐vinyl‐2‐pyrrolidone comonomers

AbstractCopolymer hydrogels were prepared through the γ irradiation of aqueous solutions composed of different ratios of acrylamide (AAm) and vinyl pyrrolidone (VP) monomers. The chemical structure, thermal stability, and structural morphology of the hydrogels were characterized with Fourier transform infrared spectroscopy, thermogravimetric analysis (TGA), and scanning electron microscopy, respectively. The IR spectroscopy analysis showed the formation of copolymerization and the presence of hydrogen bonding. The TGA study showed that the AAm/VP‐based hydrogels possessed higher thermal stability than polyacrylamide (PAAm). However, the thermal stability of the AAm/VP hydrogels increased with an increasing ratio of the VP component. The study of the swelling kinetics in water showed that all the hydrogels reached the equilibrium state after 24 h. However, the AAm/VP‐based hydrogels showed swelling in water that was lower than that of the hydrogel based on pure AAm. Meanwhile, the degree of swelling of the AAm/VP‐based hydrogels decreased with an increasing ratio of VP in the feeding solutions. The results showed that the PAAm and AAm/VP‐based hydrogels prepared at 50 kGy were affected by a change in the temperature around 25°C, whereas the hydrogels prepared at 25 kGy did not show this characteristic. However, the hydrogels prepared at different doses displayed reversible pH character. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007

A Novel N‐Succinylchitosan‐graft‐Polyacrylamide/Attapulgite Composite Hydrogel Prepared through Inverse Suspension Polymerization

AbstractA novel N‐succinylchitosan‐graft‐polyacrylamide/attapulgite composite hydrogel was prepared by using N‐succinylchitosan, acrylamide and attapulgite through inverse suspension polymerization. The result from FTIR spectra showed that OH of attapulgite, OH and NHCO of N‐succinylchitosan participated in graft polymerization with acrylamide. The introduced attapulgite could enhance thermal stability of the hydrogel. Scanning electron microscopy observation indicates that the composite hydrogel has a microporous surface. The volume ratio of heptane to water, weight ratio of acrylamide to N‐succinylchitosan and attapulgite content have great influence on swelling ability of the composite hydrogel. The composite hydrogel shows higher swelling rate and pH‐sensitivity compared to that of without attapulgite.magnified image

Characterization and Utilization of Polystyrene and Polyacrylamide-Graft-Methoxypolyethylene as Cement Admixtures

A series of polystyrene-g-methoxypolyoxyethylene (PS-g-MPOE) was prepared by solution polymerization technique using benzoyl peroxide as an initiator and another series of polyacrylamide-g-methoxypolyoxyethylene (PAM-g-MPOE) was prepared by using potassium persulfate initiator. The prepared grafted copolymers were characterized by infrared (IR), thermogravimetric analysis (TGA) and rheological properties. The results illustrated that the solution of PS-g-MPOE in water behaved as a Newtonian fluid, but the solution of PAM-g-MPOE as pseudoplastic at higher acrylamide ratios. The TGA analysis showed that the thermal stability of PAM-g-MPOE was highest. Some of these polymers were evaluated as cement admixtures. The water of consistency and setting time of the cement pastes premixed with the polymers decreased sharply than those of the blank, i.e., these polymer admixtures can act as superplastisizers and at the same time as accelerators. The combined water and free lime contents as well as compressive strength of the cement pastes premixed with PS-g-MPOE or PAM-g-MPOE were slightly lower than the blank at the early ages up to 7 d, and then became higher during the later hydration ages. Their total porosities are higher during the early ages and lower during the later ages of hydration. The SEM images confirmed that the addition of the organic polymer solutions to the cement powder does not affect the chemical composition of the normal hydration products, but only affects the physical state, shape or morphology and size of crystals of the formed hydrates.

Graft copolymerization of acrylamide onto cellulose in presence of comonomer using ceric ammonium nitrate as initiator

AbstractThe graft copolymerization of acrylamide (AAm) and ethylmethacrylate (EMA) monomers onto cellulose has been carried out using ceric ammonium nitrate (CAN) as initiator in presence of nitric acid at (25 ± 1)°C and varying feed molarity from 7.5 × 10−2 mol dm−3 to 60.0 × 10−2 mol dm−3 at fixed feed composition (fAAm = 0.6). The graft yield (%GY) has shown a linear increasing trend upto a feed molarity of 37.5 × 10−2 mol dm−3. The composition of grafted copolymer chains was found to be constant (FAAm = 0.56) during feed molarity variation but shown variations with feed composition (fAAm) and reaction temperature. The grafting parameters have shown increasing trends up to 7.5 × 10−3 mol dm−3 concentration of ceric (IV) ions and decreased on further increasing the concentration of ceric (IV) ions beyond 7.5 × 10−3 mol dm−3. The IR and elemental analysis data were used to determine the composition of grafted chains (FAAm) and reactivity ratio of acrylamide (r1) and ethylmethacrylate (r2) comonomers. The reactivity ratio for acrylamide (r1) and ethylmethacrylate (r2) has been found to be 0.7 and 1.0 respectively, which suggested for an alternate arrangement of average sequence length of acrylamide (mM̄1) and ethylmethacrylate (mM̄2) in grafted chains. The rate of graft copolymerization of comonomers onto cellulose was found to be proportional to square concentration of comonomers and square root to the concentration of ceric (IV) ions. The energy of activation (ΔEa) of graft copolymerization was found to be 9.57 kJ mol−1 within the temperature range of 20–50°C. On the basis of experimental findings, suitable reaction steps have been proposed for graft copolymerization of selected comonomers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2546–2558, 2006

Low Temperature Initiation by 3-Mercaptopropionic Acid-Ce(IV) or -KMnO4 Redox System for Polymerization of Acrylamide Monomer

ABSTRACT Polymerization of acrylamide monomer was performed at low temperatures using 3-mercaptopropionic acid-cerium(IV) sulfate and 3-mercaptopropionic acid-KMnO4 redox systems in acid aqueous medium. Water soluble polyacrylamides containing 3-mercaptopropionic acid end groups were synthesized. The effects of mole ratio of acrylamide to initiator(nMSA= nCe(IV)), polymerization time, temperature, and concentration of sulfuric acid on the yield and molecular weight of polymer were investigated. The decrease in the mole ratio of acrylamide/Ce(IV) at constant monomer concentration resulted in an increase in the yield but a decrease in molecular weight of polymer. The increase of reaction temperature from 20° to 70°C resulted in a decrease in the yield but indicated generally a constant value for the molecular weight of polymer. With increasing of polymerization time, the yield and molecular weight of polymer did not change mainly. Ce(IV) and Mn(VII) ions are reduced to Ce(III) and Mn(II) ions, respectively in the polymerization reaction. The existence of Ce(III) ion bonded to polymer was investigated by UV-visible spectrometry and fluorescence measurements. The amount of Mn(II) that is incorporated to the polymer was determined using graphite furnace atomic absorption spectrometry. The mechanism of this phenomenon is discussed.

Reactivity ratios of acrylamide–vinyl pyrrolidone copolymerization system obtained by sequential sampling

AbstractFree‐radical copolymerization of vinyl pyrrolidone and acrylamide was performed in water at 60°C. Their copolymerization reactions were continued up to high conversions and reaction mixture sampled sequentially during the reaction. The compositions of the aliquots were measured by UV spectroscopy, and their polymer contents were obtained by gravimetry. Data are evaluated by a recent error in variables method developed for sequential sampling. Reactivity ratios are found as rA = 2.03 ± 0.14, rVP = 0.09 ± 0.02. Analysis of the data up to 45% conversion by the Extended Kelen Tüdös method gave consistent results. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3822–3827, 2006

Impact of extraction conditions on the content of acrylamide in model systems and food

It has recently been suggested that the analytical methods that have been developed to date for the determination of acrylamide (AA) may underestimate the concentration of AA in certain foods, because significantly higher results were obtained upon extraction of the food matrix under alkaline conditions. The present study employs food (potato, rye) and chemical model systems to better understand the tentative release of AA under high pH extraction conditions. The experimental design is based on the generation of AA in an environment containing an AA-isotopomer, and by comparing the ratio of AA, respectively the AA-isotopomer, after extraction at pHs 7 and 12. The results show that the additional AA released is not due to improved extractability of AA from the food matrix, and should therefore be regarded as an extraction artefact. Strongly alkaline conditions seem to induce net formation of AA from water-soluble precursors formed during thermolysis.

Ceric(IV) ion‐induced graft copolymerization of acrylamide and ethyl acrylate onto cellulose

AbstractGraft copolymerization of acrylamide (AAm) and ethyl acrylate (EA) onto cellulose has been carried out from their binary mixtures using ceric ammonium nitrate (CAN) as an initiator in the presence of nitric acid at 25 ± 1 °C. The extent of acrylamide grafting increased in the presence of the EA comonomer. The composition of the grafted chains (FAAm = 0.52) was found to be constant during the feed molarity variation from 7.5 × 10−2 to 60.0 × 10−2 mol L−1, whereas the composition of the grafted chains (FAAm) was found to be dependent on feed composition (fAAm) and reaction temperature. The effects of ceric(IV) ion concentration, reaction time and temperature on the grafting parameters have been studied. The grafting parameters showed an increasing trend up to 6.0 × 10−3 mol L−1 concentration of CAN at a feed molarity of 30.0 × 10−2 mol L−1 and showed a decreasing trend on further increasing the concentration of CAN (&gt;6.0 × 10−3 mol L−1) at a constant concentration of nitric acid (5.0 × 10−2 mol L−1). The composition of the grafted chains (FAAm) was determined by IR spectroscopy and nitrogen content and the data obtained then used to determine the reactivity ratios of the acrylamide (r1) and ethyl acrylate (r2) comonomers by using a Mayo and Lewis plot. The reactivity ratios of acrylamide and ethyl acrylate were found to be r1 = 0.54 and r2 = 1.10, respectively, and hence the sequence lengths of acrylamide (m̄M1) and ethyl acrylate (m̄M2) in the grafted chains are arranged in an alternating form, as the product of the reactivity ratios of acrylamide and ethyl acrylate (r1 × r2) is less than unity. The rate of graft copolymerization of the comonomers onto cellulose was found to be dependant on the ‘squares’ of the concentrations of the comonomers and on the ‘square root’ of the concentration of ceric ammonium nitrate. The energy of activation (ΔEa) of graft copolymerzation was found to be 5.57 kJ mol−1 within the temperature range from 15 to 50 °C. On the basis of the results, suitable reaction steps have been proposed for the graft copolymerzation of acrylamide and ethyl acrylate comonomers from their mixtures. Copyright © 2005 Society of Chemical Industry

Oxidative polymerization of acrylamide in the presence of thioglycolic acid

Abstract Chemical polymerization of acrylamide at room temperature was examined by using thioglycolic acid-cerium (IV) sulfate and thioglycolic acid-KMnO4 redox systems in acid aqueous medium. Water soluble polyacrylamides containing thioglycolic acid end groups were synthesized. The effects of the molar ratio of acrylamide to Ce(IV) nAAm/nCe(IV), the polymerization time, the temperature, the monomer concentration, the molar ratio of cerium (IV) sulfate to thioglycolic acid and the concentration of sulfuric acid on the yield and molecular weight of polymer were investigated. Lower molar ratios of acrylamide/Ce(IV) at constant monomer concentration resulted in an increase in the yield but a decrease in molecular weight of polymer. The increase of reaction temperature from 20 to 70°C resulted in a decrease in the yield but generally resulted in a constant value for the molecular weight of polymer. With increasing polymerization time, the yield and molecular weight of polymer did not change substantially. Ce(IV) and Mn(VII) ions are reduced to Ce(III) and Mn(II) ions respectively in the polymerization reaction. The existence of Ce(III) ion bound to polymer was investigated by UV-visible spectrophotometry and fluoresce measurements. The amount of Mn(II) incorporated into the polymer was determined using graphite furnace atomic absorption spectrometry. The mechanism of this phenomenon is discussed.

Preparation of starch‐graft‐poly(acrylamide)/attapulgite superabsorbent composite

AbstractA novel starch‐graft‐poly(acrylamide)/attapulgite superabsorbent composite was synthesized by graft copolymerization reaction of starch, acrylamide (AM), and attapulgite micropowder using N.N‐methylene‐bisacrylamide (MBA) as a crosslinker and ammonium persulphate (APS) as an initiator in aqueous solution, followed by hydrolysis with sodium hydroxide. The effects on water absorbency, such as amount of crosslinker, initiator, attapulgite, weight ratio of acrylamide to starch in the feed, gelatinization conditions of starch and molar ratio of NaOH to acrylamide, and so forth, were investigated. These superabsorbent composites were characterized by Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The water absorbencies for these superabsorbent composites in water and saline solution were investigated, and water retention tests were carried out. Results obtained from this study showed that the water absorbency of superabsorbent composite synthesized under optimal synthesis conditions with an attapulgite content of 10% exhibit absorption of 1317 g H2O/g sample and 68 g H2O/g sample in distilled water and in 0.9 wt % NaCl solution, respectively. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1351–1357, 2005

Targeting normal and neoplastic tissues in the rat jejunum and colon with boronated, cationic acrylamide copolymers

A series of boronated cationic copolymers, composed of different ratios of acrylamide, N-acryloyl-3-aminophenylboronic acid and N-acryloyl-diaminoethane (the cationic moiety), were prepared with the intention of localizing boron neutron capture therapy (BNCT) in experimentally induced polyps on the luminal side of the gut of the rat. The goals of this study were to: (a) test the effect of cationization of the boronated copolymers on their uptake by polyps and normal adjacent epithelium; (b) compare the whole rat body distribution of aminophenylboronic acid (APB) and polymeric APB after local application; (c) measure the effect of micro-environmental parameters such as pH, the presence of mucin and cations on the interaction between the APB-copolymers and the epithelium of the rat intestines. Direct analysis of tissue boron levels showed that polymeric APB-uptake was higher in the colonic polyps than in the surrounding normal tissues. Free APB, however, was found in similar quantities in both. When tested in the normal jejunum and colon of the rat, polymeric APB uptake was directly proportional to the molar content of the cationic monomer in the copolymers. The presence of magnesium ions, free boron cationic monomer and mucin interfered with this uptake in a concentration-dependent manner. The uptake was pH-independent at pH 5, 7 and 10. APB accumulation in the colon polyps was inversely proportional to the cationic monomer content in the copolymers, suggesting an increased amount of mucus around the polyps, which probably impeded the electrostatic attachment of the polymer to the malignant tissue. The use polymeric APB for targeting BNCT in perioperative treatment of colorectal carcinoma is suggested, especially in the cases of microscopic residual disease after curative resection.

Structure and Dynamics of Micelle-bound Human α-Synuclein

Misfolding of the protein alpha-synuclein (aS), which associates with presynaptic vesicles, has been implicated in the molecular chain of events leading to Parkinson's disease. Here, the structure and dynamics of micelle-bound aS are reported. Val3-Val37 and Lys45-Thr92 form curved alpha-helices, connected by a well ordered, extended linker in an unexpected anti-parallel arrangement, followed by another short extended region (Gly93-Lys97), overlapping the recently identified chaperone-mediated autophagy recognition motif and a highly mobile tail (Asp98-Ala140). Helix curvature is significantly less than predicted based on the native micelle shape, indicating a deformation of the micelle by aS. Structural and dynamic parameters show a reduced helical content for Ala30-Val37. A dynamic variation in interhelical distance on the microsecond timescale is complemented by enhanced sub-nanosecond timescale dynamics, particularly in the remarkably glycine-rich segments of the helices. These unusually rich dynamics may serve to mitigate the effect of aS binding on membrane fluidity. The well ordered conformation of the helix-helix connector indicates a defined interaction with lipidic surfaces, suggesting that, when bound to larger diameter synaptic vesicles, it can act as a switch between this structure and a previously proposed uninterrupted helix.

Determination of monomer apparent reactivity ratios for acrylonitrile-acrylamide copolymerization system

Effect of copolymerization systems on monomer apparent reactivity ratios for copolymer of acrylonitrile with acrylamide was studied for contrast. Values of monomer apparent reactivity ratios were calculated by Kelen-Tudos method. It has been found that the apparent reactivity ratios in aqueous suspension polymerization system were similar to those in solution polymerization system at polymerization conversion less than 18% [reactivity ratio of acrylonitrile (rAN) = 0.398± 0.004, reactivity ratio of acrylamide (rAM) = 2.61± 0.02]. As conversion of more than 60%, the changes of monomer apparent reactivity ratios become less prominent (rAN = 0.651± 0.008, rAM = 1.98± 0.01). In water-rich reaction medium [(H2O/dimethylsulfoxide (DMSO) > 80/20), monomer apparent reactivity ratios were approximately equivalent to those in aqueous suspension polymerization system. In DMSO-rich reaction medium (DMSO/H2O > 80/20), apparent reactivity ratios were similar to those in solution polymerization system. With an increase of polarity of solvent, values of apparent reaction ratios both decreased. The values of apparent reaction ratios gradually tend to 1 with increasing the copolymerization temperature.

Modulation of dynamic release of vitamin B2 from a model pH‐sensitive terpolymeric hydrogel system

AbstractTerpolymeric devices consisting of acrylamide, methacrylamide and acrylic acid were synthesized and the release of the model drug riboflavin from these devices was studied at the physiological temperature 37°C. The gels exhibit a sharp pH‐dependent release behavior. The devices released nearly 42.2 ± 2.6% drug at pH 1.0 while nearly 95.3 ± 3.2% drug was released at pH 7.4. With increasing concentration of cross‐linker in the gel, the drug released was found to decrease. Moreover, with low content of cross‐linker a nearly zero‐order profile was obtained. The size of the cylindrical devices also affected the release kinetics and a linear dependency was observed between t1/2 (ie, the time required for 50 % release) and the square of the diameter, thus supporting the Tanaka–Fillmore theory. The molar ratio of acrylamide and methacrylamide also affected the dynamic release of riboflavin. It was found that variation in transit time could also affect the drug‐releasing capacity of the devices. Finally, the average and ‘late‐time’ diffusion coefficients for the gels having different initial loads were also evaluated. Copyright © 2004 Society of Chemical Industry

Modulation of the sensitive temperature range of fluorescent molecular thermometers based on thermoresponsive polymers.

Fluorescent molecular thermometers based on polymers showing a temperature-induced phase transition and labeled with polarity-sensitive fluorescent benzofurazans are the most sensitive known. Here we show a simple and effective method for modulating the sensitive temperature ranges of fluorescent molecular thermometers based on such temperature-responsive polymers. 4-N-(2-acryloyloxyethyl)-N-methylamino-7-N,N-dimethylaminosulfonyl-2,1,3-benzoxadiazole was adopted as a polarity-sensitive fluorescent benzofurazan, and nine copolymers of two kinds of acrylamide derivative (N-n-propylacrylamide, N-isopropylacrylamide, and/or N-isopropylmethacrylamide) with a small amount of DBD-AE were obtained. The fluorescence intensities of these copolymers in aqueous solution sharply increased with increasing temperature over a small range (6-7 degrees C). In contrast, these fluorescent molecular thermometers differed from one another in the sensitive temperature range (between 20 and 49 degrees C). Moreover, the sensitive temperature ranges were well related to the acrylamide ratios in feed. In addition, the responses from these fluorescent molecular thermometers to the change in temperature were reversible and exactly repeatable during 10 cycles of heating and cooling (relative standard deviation of the fluorescence intensity, 0.44-1.0%).