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Acid Monomers (acid + monomer)
Kinds of Acid Monomers Selected AbstractsChemInform Abstract: Synthesis of Uracil Derivatives and Their Alkylation: An Approach to Peptide Non-nucleic Acid Monomers.CHEMINFORM, Issue 37 2010Madhukar N. Jachak Abstract The introduction of various functionalities at N-1 position of uracils (II) leads to derivatives of type (IV). [source] Effect of the carboxylic acid monomer type on the emulsifier-free emulsion copolymerization of styrene and butadieneJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007Mahdi Abdollahi Abstract Carboxylated styrene,butadiene rubber latexes were prepared through the emulsifier-free emulsion copolymerization of styrene and butadiene with various carboxylic acid monomers. The effects of various carboxylic acid monomers on the particle formation process were investigated. The type of carboxylic acid monomer strongly affected the particle nucleation. The number of particles and thus the polymerization rate increased with the increasing hydrophobicity of the carboxylic acid monomers. There was a significant difference in the polymerization rate per particle. The results showed that particle nucleation and growth were dependent on the hydrophilic nature of the carboxylic acid monomers. The average particle diameter of the carboxylated styrene,butadiene rubber latexes in the dry state was obtained through some calculations using direct measurements of the average particle diameter in the monomer-swollen state by a dynamic light scattering technique. Several parameters, such as the polymerization rate, number of latex particles per unit of volume of the aqueous phase, and polymerization rate per particle, were calculated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] ,Smart' delivery systems for biomolecular therapeuticsORTHODONTICS & CRANIOFACIAL RESEARCH, Issue 3 2005PS Stayton Structured Abstract Authors ,, Stayton PS, El-Sayed MEH, Murthy N, Bulmus V, Lackey C, Cheung C, Hoffman AS Objective ,, There is a strong need for drug delivery systems that can deliver biological signals from biomaterials and tissue engineering scaffolds, and a particular need for new delivery systems that can efficiently deliver biomolecules to intracellular targets. Viruses and pathogens have evolved potent molecular machinery that sense the lowered pH gradient of the endosomal compartment and become activated to destabilize the endosomal membrane, thereby enhancing protein or DNA transport to the cytoplasmic compartment. A key feature of many of these biological delivery systems is that they are reversible, so that the delivery systems are not directly toxic. These delivery systems have the ability to change their structural and functional properties and thus display remarkable ,smart' material properties. The objective of this presentation is to review the initial development of smart polymeric carriers that mimic these biological delivery systems and combine similar pH-sensitive, membrane-destabilizing activity for the delivery of therapeutic biomolecules. Design ,, We have developed new ,smart' polymeric carriers to more effectively deliver and broaden the available types of biomolecular therapeutics. The polymers are hydrophilic and stealth-like at physiological pH, but become membrane-destabilizing after uptake into the endosomal compartment where they enhance the release of therapeutic cargo into the cytoplasm. They can be designed to provide a range of pH profiles and membrane-destabilizing activities, allowing their molecular properties to be matched to specific drugs and loading ranges. A versatile set of linker chemistries is available to provide degradable conjugation sites for proteins, nucleic acids, and/or targeting moieties. Results ,, The physical properties of several pH-responsive polymers were examined. The activity and pH profile can be manipulated by controlling the length of hydrophobic alkyl segments. The delivery of poly(propyl acrylic acid) (PPAA)-containing lipoplexes significantly enhanced wound healing through the interconnected effects of altered extracellular matrix organization and greater vascularization. PPAA has also been shown to enhance cytoplasmic delivery of a model protein therapeutic. Polymeric carriers displaying pH-sensitive, membrane-destabilizing activity were also examined. The pH profile is controlled by the choice of the alkylacrylic acid monomer and by the ratio of the carboxylate-containing alkylacrylic acid monomer to alkylacrylate monomer. The membrane destabilizing activity is controlled by the lengths of the alkyl segment on the alkylacrylic acid monomer and the alkylacrylate monomer, as well as by their ratio in the final polymer chains. Conclusion ,, The molecular mechanisms that proteins use to sense and destabilize provide interesting paradigms for the development of new polymeric delivery systems that mimic biological strategies for promoting the intracellular delivery of biomolecular drugs. The key feature of these polymers is their ability to directly enhance the intracellular delivery of proteins and DNA, by destabilizing biological membranes in response to vesicular compartment pH changes. The ability to deliver a wide variety of protein and nucleic acid drugs to intracellular compartments from tissue engineering and regenerative scaffolds could greatly enhance control of important processes such as inflammation, angiogenesis, and biomineralization. [source] The preparation and properties of dextrin-graft-acrylic acid/montmorillonite superabsorbent nanocompositePOLYMER COMPOSITES, Issue 7 2009Xin Ding A novel superabsorbent nanocomposite was synthesized through intercalation polymerization of partially neutralized acrylic acid, gelatinized dextrin, and an organic-montmorillonite powder using N,N -methylenebisacrylamide as a crosslinker, Span-60 as a dispersant, and ammonium persulfate together with sodiumsulfite as a type of mixed redox initiator. Effects of the amount of them on water absorbency of the superabsorbent were investigated. The structure and the morphology of the nanocomposite were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, and transmission electron microscopy analysis. The blood compatibility of the composite was primarily measured. The results show that the acrylic acid monomer was successfully intercalated into the organic-montmorillonite layers and bonded with them. The superabsorbent nanocomposite synthesized under optimal conditions with an organic-montmorillonite powder content of 5 wt% exhibit an absorption of 725.3 g/g in distilled water and favorable blood compatibility. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source] Performance evaluation of synthesized acrylic acid grafted polypropylene within CaCO3/polypropylene compositesPOLYMER COMPOSITES, Issue 2 2000F. Rahma A polymeric coupling agent acrylic acid grafted polypropylene (AAgPP) was synthesized and its efficiency in CaCO3/PP composite was investigated. The grafting of acrylic acid monomer (AA) onto polypropylene was performed using an internal mixer. The effect of peroxyde, acrylic acid monomer content, temperature and RPM was studied. A grafting reaction between the polypropylene and the acrylic acid was evidenced through FTIR, UV, DSC and MFI testing. The highest grafting yield was obtained at 0.85 phr peroxide and 5 phr acrylic acid. The selected mixing temperature was 200°C, the rotor speed 150 rpm and the residence time 5 min. The obtained coupling agent (AAgPP) was used with 30 wt% CaCO3 filled polypropylene. Strong interactions with the composite were observed. The effect of increasing the coupling agent content on Izod impact and tensile properties was investigated. A maximum in the above properties is attained at 15 wt% AAgPP. The most important effect is clearly shown in the Izod test. In fact, a threefold increase has been observed for either notched and untoched specimen. The 15 wt% AAgPP is considered to be a critical concentration for the composite considered. This corresonds to maximum interactions occurring between the matrix and the filler. SEM analysis clearly shows strong interactions between the filler and the matrix in the presence of acrylic acid grafted polypropylene. This is another proof of the efficiency of the synthesized AAgPP as a potential coupling agent for CaCO3 filled PP. [source] Interpenetrating polymeric network hydrogels for potential gastrointestinal drug releasePOLYMER INTERNATIONAL, Issue 11 2007Sema Ekici Abstract New interpenetrating polymeric network (IPN) hydrogels based on chitosan (C), poly(N -vinyl pyrrolidone) (PVP) and poly(acrylic acid) (PAAc), crosslinked with glutaraldehyde (G) and N,N,-methylenebisacrylamide (MBA), were prepared and investigated for potential gastrointestinal drug delivery vehicles utilizing a model drug, amoxicillin. IPN hydrogels were synthesized by simultaneous polymerization/crosslinking of acrylic acid monomer in the presence of another polymer (C) and crosslinker (G, MBA). Three different concentrations of glutaraldehyde were used (0.5, 1.0 and 2.0 w/w) to control the overall porosity of the hydrogels, named C-P-AAc/0.5, C-P-AAc/1.0 and C-P-AAc/2.0, respectively. Spectroscopic and thermal analyses such as Fourier transform infrared spectroscopy, thermogravimetric analysis and thermomechanical analysis were performed for IPN characterization. Equilibrium swelling studies were conducted for pH and temperature response behavior. Swelling studies were also carried out in simulated gastric fluid of pH = 1.1 and simulated intestinal fluid of pH = 7.4 to investigate possible site-specific drug delivery. It was found that the release behavior of the drug from these IPN hydrogels was dependent on the pH of the medium and the proportion of crosslinker in the IPN. It was observed that amoxicillin release at pH = 7.4 was higher than at pH = 1.1. The analysis of the drug release showed that amoxicillin was released from these hydrogels through a non-Fickian diffusion mechanism. Copyright © 2007 Society of Chemical Industry [source] Modification of polystyrene properties through grafting with N -vinylcarboxamido-2-methylpropane sulfonic acid monomerPOLYMER INTERNATIONAL, Issue 12 2004A Aggour Abstract Polystyrene (PS) possesses good mechanical properties, but its surface is relatively inert and hydrophobic. Grafting of N -vinylcarboxamido-2-methylpropane sulfonic acid (VCMP) is useful to hydrophilize the PS surface. Grafting was performed using benzoyl peroxide (BPO) as an initiator in toluene:methanol solvent mixture (3:1 volume ratio). The influence of the main factors on grafting, such as temperature, time, concentrations of initiator, PS and VCMP, has been studied. The results show that the initial rate of polymerization and percentage of grafting are enhanced by increased temperature. Furthermore, the specific rate constants of the first order reaction/are determined, and the activation energy of the grafting reaction is estimated. The grafting parameters are established and a suitable mechanism of the reaction is proposed. The grafted PS is to characterized through infrared spectra, intrinsic viscosity, thermogravimetric analysis (TGA) and differential gravimetric analysis (DTG). The kinetics of thermal degradation and the order of the thermal stabilities are given. Also the decomposition activation energies of the thermal degradation are determined, and confirm the thermal stabilities of the polymers used. © 2004 Society of Chemical Industry [source] Flow-Through Assay of Quinine Using Solid Contact Potentiometric Sensors Based on Molecularly Imprinted PolymersELECTROANALYSIS, Issue 24 2009Ayman Abstract Miniaturized potentiometric membrane sensors for quinine incorporated with molecular imprinted polymer (MIP) were synthesized and implemented. Planar PVC based polymeric membrane sensors containing quinine-methacrylic and/or acrylic acid-ethylene glycol methacrylate were dispensed into anisotropically etched wells on polyimide wafers. The determination of quinine was carried out in acidic solution at pH,6, where positively charged species predominated prevalently. The suggested miniaturized planner sensors exhibited marked selectivity, sensitivity, long-term stability and reproducibility. At their optimum conditions, the sensors displayed wide concentration ranges of 4.0×10,6,1.0×10,2mol L,1 and 1.0×10,5,1.0×10,2 mol L,1 with slopes of about 61.3,55.7,mV decade,1; respectively. Sensors exhibit detection limits of 1.2×10,6 and 8.2×10,6 mol L,1 upon the use of methacrylic and acrylic acid monomers in the imprinted polymer, respectively. Validation of the assay method according to the quality assurance standards (range, within-day repeatability, between-day variability, standard deviation, accuracy, and good performance characteristics) which could assure good reliable novel sensors for quinine estimation was justified. Application of the proposed flow-through assay method for routine determination of quinine in soft drinks was assayed and the results compared favorably with data obtained by the standard fluorimetric method. [source] Cyclic fatty acids in sunflower oils during frying of frozen foods with oil replenishment,EUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, Issue 2 2007Antonio Romero Abstract Frying of frozen foods has become popular because it considerably reduces cooking time. Polymers and cyclic fatty acid monomers (CFAM) formed during frying are potentially toxic and therefore their production should be minimized. Twenty discontinuous fryings of different frozen foods were carried out over ten consecutive days, in sunflower oil (SO) and in high-oleic acid sunflower oil (HOSO), by adding fresh oil after each frying to bring the volume of the fryer oil back to 3,L. CFAM methyl ester derivates were hydrogenated, isolated, concentrated and quantified by HPLC using a reverse-phase column, followed by gas chromatography. After 20,fryings, significantly higher contents of polar material, polymers and CFAM (all p,<0.001) were found in SO than in HOSO. Bicyclic compound formation was four times higher in SO (p,<0.001). The fat from the fried potatoes presented a polymer content very similar to that of their corresponding oils. The 100-g rations of the SO-fried potatoes from the 20th frying supply 49 or 15%, respectively, more polymers and CFAM and 1,mg more bicyclic fatty acids than the 100-g rations of HOSO-fried potatoes. Because digestion and absorption of polar material, polymers and CFAM occur, the data clearly show the advantageousness and advisability of frying with HOSO rather than SO. [source] Effect of the carboxylic acid monomer type on the emulsifier-free emulsion copolymerization of styrene and butadieneJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007Mahdi Abdollahi Abstract Carboxylated styrene,butadiene rubber latexes were prepared through the emulsifier-free emulsion copolymerization of styrene and butadiene with various carboxylic acid monomers. The effects of various carboxylic acid monomers on the particle formation process were investigated. The type of carboxylic acid monomer strongly affected the particle nucleation. The number of particles and thus the polymerization rate increased with the increasing hydrophobicity of the carboxylic acid monomers. There was a significant difference in the polymerization rate per particle. The results showed that particle nucleation and growth were dependent on the hydrophilic nature of the carboxylic acid monomers. The average particle diameter of the carboxylated styrene,butadiene rubber latexes in the dry state was obtained through some calculations using direct measurements of the average particle diameter in the monomer-swollen state by a dynamic light scattering technique. Several parameters, such as the polymerization rate, number of latex particles per unit of volume of the aqueous phase, and polymerization rate per particle, were calculated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Sources and Mechanisms of Carbon Monoxide Production by IrradiationJOURNAL OF FOOD SCIENCE, Issue 6 2004E.J. Lee ABSTRACT: The sources and mechanisms of gas production by irradiation were determined using model systems prepared with fatty acid, phospholipids, oil, sugars, glycolysis and TCA cycle intermediates, nucleic acids, amino acid monomers and homopolymers, and proteins. The model systems were irradiated at 0, 2.5, 5, or 10 kGy using a linear accelerator and the amounts of CO, CO, and CH produced were determined using gas chromatography. The productions of CO, CO2, and CH4 in all samples were irradiation-dose dependent. Glycine, asparagine, and glutamine were the major sources of CO production among amino acids, and glyceraldehydes, pyruvate, and ,-ketoglutarate were the major sources of CO among glycolysis intermediates. Phosphatidyl choline, phosphatidyl ethanolamine, and lysophosphatidyl choline produced the greatest amounts of CO among the phospholipids. The major sources of CO2 production were pyruvate, threoine, and methionine, and those of CH4 were methionine and acetone. The amounts of CO produced from these sources were significant, and the production of gas compounds via radiolytic degradation appears to be closely related to the structure of molecules. [source] RAFT polymerization of styrenic-based phosphonium monomers and a new family of well-defined statistical and block polyampholytesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2007Ran Wang Abstract We describe herein the first example of the controlled reversible addition-fragmentation chain transfer (RAFT) radical homo- and copolymerization of phosphonium-based styrenic monomers mediated with a trithiocarbonate-based RAFT chain transfer agent (CTA) directly in aqueous media. In the case of homopolymer syntheses the polymerizations proceed in a controlled fashion yielding materials with predetermined molecular characteristics as evidenced from the narrow molecular mass distributions (MMD) and the excellent agreement between the theoretical and experimentally determined molecular masses (MM). We also demonstrate the controlled nature of the homopolymerization of 4-vinylbenzoic acid with the same CTA in DMSO. We subsequently prepared both statistical and block copolymers from the phosphonium/4-vinylbenzoic acid monomers to yield the first examples of polyampholytes in which the cationic functional group is a quaternary phosphonium species. We show that the kinetic characteristics of the statistical copolymerizations are different from the homopolymerizations and proceed, generally, at a significantly faster rate although there appears to be a composition dependence on the rate. Given the inherent problems in characterizing such polyampholytic copolymers via aqueous size exclusion chromatography we have qualitatively proved their successful formation via FTIR spectroscopy. Finally, in a preliminary experiment we qualitatively demonstrate the ability of such pH-responsive block copolymers to undergo supramolecular self-assembly. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2468,2483, 2007 [source] Thiol,ene coupling reaction of fatty acid monomersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 24 2004Johan Samuelsson Abstract The reactivities and reaction rates of the thiol,ene coupling reaction of 2-ethyl-(hydroxymethyl)-1,3-propanediol trimercapto acetate and 2-ethyl-(hydroxymethyl)-1,3-propanediol trimercapto propionate with two common unsaturated fatty acid methyl esters (methyl oleate and methyl linoleate) were evaluated. The reactions were monitored with real-time IR and 1H NMR, which both showed that the mercapto acetate was more reactive than the mercapto propionate. Both thiols were more prone to add to the monounsaturated methyl oleate than to methyl linoleate, which contained two unconjugated double bonds. According to bond energy calculations, the thiol hydrogen of mercapto acetate was somewhat more difficult to abstract than the hydrogen of mercapto propionate. Consequently, the formed SC bond in the acetate case was stronger than in the propionate case, and so the equilibrium was more shifted toward the addition products. The real-time IR measurements also showed that the cis unsaturation in methyl oleate isomerized much more quickly than that in methyl linoleate, and this also had an impact on the overall addition rate of the thiols because a trans unsaturation was more reactive than a cis unsaturation. The higher isomerization rates in the oleate systems, compared with those of the linoleate systems, was suggested to be due to a more restricted rotation along the CC bond of the reacted unsaturation in linoleate. This study showed the importance of trans unsaturations in obtaining reasonable reaction rates in thiol,ene reactions with fatty acid derivatives. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 6346,6352, 2004 [source] Influence of Structure on Polymerization Rates and Ca-Binding of Phosphorus-Containing 1,6-DienesMACROMOLECULAR REACTION ENGINEERING, Issue 5 2007Aylin Ziylan Albayrak Abstract Photo- and thermal-polymerizations of 4-diethoxyphosphoryl-2,4,6-tris(ethoxycarbonyl)-1,6-heptadiene, 4,4-bis(diethoxyphosphoryl)-2,6-bis(t -butoxycarbonyl)-1,6-heptadiene and 4-diethoxyphosphoryl-4-ethoxycarbonyl-2,6-bis(t -butoxycarbonyl)-1,6-heptadiene monomers and their phosphonic and carboxylic acid derivatives were investigated to understand the effect of the cyclic monomer structure on their polymerization reactivity. A strong effect of the substituents at positions 2, 4 and 6 of the monomers on polymerization rate was observed. The polymerizability of the monomers was successfully correlated with the 13C NMR chemical shifts of the vinyl carbons. Conversion values were consistent with the Tg being a measure of the flexibility of a monomer. The monomers containing phosphonic acid groups were soluble in water and ethanol. The acidic nature of the aqueous solutions of these monomers is expected to give them etching properties, important for dental applications. The interaction of the acid monomers with hydroxyapatite was investigated using 13C NMR technique. [source] Frontal Polymerization Synthesis of Starch-Grafted Hydrogels: Effect of Temperature and Tube Size on Propagating Front and Properties of HydrogelsCHEMISTRY - A EUROPEAN JOURNAL, Issue 12 2006Qing-Zhi Yan Prof. Dr. Abstract The frontal polymerization process was used to produce superabsorbent hydrogels based on acrylic acid monomers grafted onto starch. Using a simple test tube which was nonadiabatic and permitted contact with air, the effects of initial temperature and tube size on the propagating front of grafting copolymerization and the properties of hydrogels were explored. The unrestricted access of the reaction mixture to oxygen delayed the formation of self-propagating polymerization front. The ignition time was markedly lengthened with the increasing of tube size attributed to the formation of large amounts of peroxy radicals. The front velocity dependence on initial temperature could be fit to an Arrhenius function with the average apparent activation energy of 24 kJ,mol,1, and on tube size to a function of higher order. The increase of the initial temperature increased the front temperature, which lead to more soluble oligomers and higher degree of crosslinking. The interplay of two opposite effects of oligomer and crosslinking determined the sol and gel content. An increase in tube size had two effects on the propagating front. One was to reduce heat loss. The other effect was to increase the number of escaping gas bubbles. The combined action of the two effects resulted in a maximum value of front temperature, an increase in sol content and a reduction in gel content with tube size. The highest swelling capacity of hydrogels was obtained when the initial temperature or tube size favored a formation of porous microstructure of hydrogels. [source] | |||||||||||||