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Sample records for acrylic acid-grafted coir

  1. Hemocompatibility of Chitosan/poly(acrylic acid) Grafted Polyurethane Tubing

    PubMed Central

    Lee, Hyun-Su; Tomczyk, Nancy; Kandel, Judith; Composto, Russell J.; Eckmann, David M.

    2013-01-01

    The activation and adhesion of platelets or whole blood exposed to chitosan (CH) grafted surfaces is used to evaluate the hemocompatibility of biomaterials. The biomaterial surfaces are polyurethane (PU) tubes grafted with an inner poly(acrylic acid) (PAA) and an outer CH or quaternary ammonium modified CH (CH-Q) brush. The CH, CH-Q and PAA grafted layers were characterized by ellipsometry and fluorescence microscopy. Material wear tests demonstrate that CH (CH-Q) is stably grafted onto PU tubes upon exposure to saline solution for 7 days. Using quartz-crystal microbalances with dissipation (QCM-D), in-situ adsorption of blood plasma proteins on CH and CH-Q compared to a silicon oxide control was measured. The QCM-D results showed that the physically adsorbed plasma protein layer on CH-Q and CH surfaces is softer and more viscous than the protein layer on the SiO2 surface. The CH-Q layer thus has the weakest interaction with plasma proteins. Whole blood and platelet adhesion was reduced by ~92% on CH-Q, which showed the weakest interaction with plasma protein but more viscous adsorbed plasma protein layer, compared to SiO2. Last, to examine the biologic response of platelets and neutrophils to biomaterial surfaces, CH (CH-Q)/PAA, PAA and PU tubes were tested using a Chandler Loop apparatus as an ex vivo model and flow cytometry. The blood adhesion and biologic response results showed that CH and CH-Q reduced adhesion and activation of platelets and neutrophils and improved hemocompatibility relative to other surfaces (PU and PAA). Our studies demonstrated that the properties of physically adsorbed plasma protein layer on biomaterial surfaces correlates with blood coagulation on biomaterial surfaces. PMID:24349719

  2. A density functional study on dielectric properties of acrylic acid grafted polypropylene.

    PubMed

    Ruuska, Henna; Arola, Eero; Kortelainen, Tommi; Rantala, Tapio T; Kannus, Kari; Valkealahti, Seppo

    2011-04-07

    Influence of acrylic acid grafting of isotactic polypropylene on the dielectric properties of the polymer is investigated using density functional theory (DFT) calculations, both in the molecular modeling and three-dimensional (3D) bulk periodic system frameworks. In our molecular modeling calculations, polarizability volume, and polarizability volume per mass which reflects the permittivity of the polymer, as well as the HOMO-LUMO gap, one of the important measures indicating the electrical breakdown voltage strength, were examined for oligomers with various chain lengths and carboxyl mixture ratios. When a polypropylene oligomer is grafted with carboxyl groups (cf. acrylic acid), our calculations show that the increase of the polarizability volume α' of the oligomer is proportional to the increase of its mass m, while the ratio α'/m decreases from the value of a pure polymer when increasing the mixture ratio. The decreasing ratio of α'/m under carboxyl grafting indicates that the material permittivity might also decrease if the mass density of the material remains constant. Furthermore, our calculations show that the HOMO-LUMO gap energy decreases by only about 15% in grafting, but this decrease seems to be independent on the mixture ratio of carboxyl. This indicates that by doping polymers with additives better dielectric properties can be tailored. Finally, using the first-principles molecular DFT results for polarizability volume per mass in connection with the classical Clausius-Mossotti relation, we have estimated static permittivity for acrylic acid grafted polypropylene, assuming the structural density keeping constant under grafting. The computed permittivity values are in a qualitative agreement with the recent experiments, showing increasing tendency of the permittivity as a function of the grafting composition. In order to validate our molecular DFT based approach, we have also carried out extensive three-dimensional bulk periodic first

  3. Protein absorption and fouling on poly(acrylic acid)-graft-polypropylene microfiltration membrane

    NASA Astrophysics Data System (ADS)

    Liu, Yanjun; Ma, Huiying; Lv, Chunying; Yang, Jia; Fu, Xueqi

    2009-07-01

    A series of pH-sensitive poly (acrylic acid)-graft-polypropylene hollow fiber microfiltration membranes were prepared by UV-photo-irradiation. Bovine serum albumin (BSA) was chosen as the model protein to investigate its absorption and fouling behaviors on membranes. The results showed that the hydrophilicity of grafted membrane was improved by poly(acrylic acid) chains with parts of membrane pores blocked. The grafted membranes were markedly pH-dependent on the water permeability as pH was altered from 1 to 11. The zeta potential of grafted membranes calculated by streaming potential was negative in most pH range. Electrostatic interaction energy calculated by DLVO theory showed the electric interaction force between grafted membrane and BSA was attractive. With the rise of grafting degree, the electric attractive force between grafted membrane and BSA increased as pH=3 and decreased as pH=8, while it kept basically unchanged as pH=4.7. As a result, most serious fouling was observed as pH=4.7. Grafted membranes had a lower BSA absorption and better antifouling behavior as pH=8, while the opposite result was revealed as pH=3. In conclusion, the absorption and fouling behavior of BSA on membranes was pH-dependent due to the pH-dependence of membrane charge, and the conformation of BSA and grafting chains.

  4. Removal of dorzolamide from biomedical wastewaters with adsorption onto graphite oxide/poly(acrylic acid) grafted chitosan nanocomposite.

    PubMed

    Kyzas, George Z; Bikiaris, Dimitrios N; Seredych, Mykola; Bandosz, Teresa J; Deliyanni, Eleni A

    2014-01-01

    A novel graphite oxide/poly(acrylic acid) grafted chitosan nanocomposite (GO/CSA) was prepared and used as biosorbent for the removal of pharmaceutical compound (dorzolamide) from biomedical synthetic wastewaters. The performance was evaluated taking into account pH, kinetics and thermodynamics of adsorption. GO/CSA presented higher adsorption capacity in comparison with the parent materials (graphite oxide and poly(acrylic acid) grafted chitosan). All adsorbents prepared were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and potentiometric titration. The surface features were also evaluated after the dorzolamide adsorption in order to derive the adsorption mechanism. It was suggested that the reactive groups of GO and CSA can interact with the amino groups of dorzolamide and mainly the abundance of carboxyl groups of GO/CSA composite was the main reason for its enhanced adsorption capacity.

  5. Cr(VI) adsorption from electroplating plating wastewater by chemically modified coir pith.

    PubMed

    Suksabye, Parinda; Thiravetyan, Paitip

    2012-07-15

    Coir pith samples were chemically modified by grafting with acrylic acid for the removal of Cr(VI) from electroplating wastewater. The presence of acrylic acid on the coir pith surface was verified by a scanning electron microscope with an electron dispersive x-ray spectrometer (SEM/EDX), Fourier transform infrared spectroscopy (FTIR) and thermogravimetry (TG). The carbonyl groups (C==O) from the carboxylic acids (COOH) increased on the coir pith surface after grafting with acrylic acid. In addition, the thermal stability of the acrylic acid-grafted coir pith also improved. The optimum conditions for grafting the acrylic acid on the coir pith consisted of 2 M acrylic acid and 0.00125 M ceric ammonium nitrate (CAN, as an initiator). The maximum Cr(VI) removal (99.99 ± 0.07%) was obtained with the following conditions: a 1.3% (w/v) dosage of acrylic acid-grafted coir pith, a system pH of 2, a contact time of 22 h, a temperature of 30 °C, a particle size of <150 μm and an initial Cr(VI) of 1,171 mg l(-1). At system pH of 2, Cr(VI) in the HCrO(4)(-) form can be adsorbed with acrylic acid-grafted coir pith via an electrostatic attraction. The adsorption isotherm of 2 M acrylic acid-grafted coir pith exhibited a good fit with the Langmuir isotherm. The maximum Cr(VI) adsorption capacity of the 2 M acrylic acid-grafted coir pith was 196.00 mg Cr(VI) g(-1) adsorbent, whereas for coir pith without grafting, the maximum Cr(VI) removal was 165.00 mg Cr(VI) g(-1) adsorbent. The adsorption capacity of the acrylic acid-grafted coir pith for Cr(VI) was higher compared to the original coir pith. This result was due to the enhancement of the carbonyl groups on the coir pith surface that may have involved the mechanism of chromium adsorption. The X-ray absorption near edged structure (XANES) and desorption studies suggested that most of the Cr(III) that presented on the acrylic acid-grafted coir pith was due to the Cr(VI) being reduced to Cr(III) on the adsorbent surface. FTIR

  6. Optimization of acrylic acid grafting onto polypropylene using response surface methodology and its biodegradability

    NASA Astrophysics Data System (ADS)

    Mandal, Dev K.; Bhunia, Haripada; Bajpai, Pramod K.; Kushwaha, Jai P.; Chaudhari, Chandrasekhar V.; Dubey, Kumar A.; Varshney, Lalit

    2017-03-01

    Simultaneous radiation grafting was optimized to graft acrylic acid monomer on the polypropylene (PP) films to make them hydrophilic and enhance their biodegradability. Experiments were designed based on full factorial central composite design (response surface methodology) and influence of monomer concentration, radiation dose, inhibitor concentration, solvent concentration on degree of grafting was investigated. The extent of grafting was found to increase with increasing monomer concentration, inhibitor concentration and radiation dose. The targeted 35% grafting could be achieved at optimum condition viz. monomer concentration 12.09 wt%, radiation dose 12.40 kGy, inhibitor concentration 0.07 M and solvent concentration 0.12 M. The grafted PP films at different degrees of grafting were tested for tensile properties and characterized by swelling studies, fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). Successful grafting of acrylic acid onto polypropylene films was indicated by FTIR and confirmed quantitatively by determination of carboxylic groups on the film surface. Tensile strength of grafted PP films decreased with increase in degree of grafting. The crystallinity of the grafted PP films was lower than that of PP film as indicated by DSC studies. Grafting of acrylic acid increased the roughness on the surface of PP films indicated by SEM studies. The maximum biodegradability of the 34.55% grafted film was 5.5%.

  7. Poly(acrylic acid)-grafted poly(N-isopropyl acrylamide) networks: preparation, characterization and hydrogel behavior.

    PubMed

    Yu, Rentong; Zheng, Sixun

    2011-01-01

    Poly(acrylic acid)-grafted poly(N-isopropylacrylamide) co-polymer networks (PNIPAAm-g-PAA) were prepared via the reversible addition-fragmentation transfer (RAFT) polymerization of N-isopropyl- acrylamide (NIPAAm) with trithiocarbonate-terminated PAA as a macromolecular chain-transfer agent in the presence of N,N-methylenebisacrylamide. The PNIPAAm-g-PAA co-polymer networks were characterized by means of Fourier transform infrared spectroscopy, differential scanning calorimetry and small-angle X-ray scattering. It is found that the PNIPAAm-g-PAA co-polymer networks were microphase-separated, in which the microdomains of PNIPAAm-PAA interpolymer complexes were dispersed into the PNIPAAm matrix. The PNIPAAm-g-PAA hydrogels displayed a dual response to temperature and pH values. The thermoresponsive properties of PNIPAAm-g-PAA networks were investigated. Below the volume phase transition temperatures, the PNIPAAm-g-PAA hydrogels possessed much higher swelling ratios than control PNIPAAm hydrogel. In terms of swelling, deswelling and reswelling tests, it is judged that the PNIPAAm-g-PAA hydrogels displayed faster response to the external temperature changes than control PNIPAAm hydrogel. The improved thermoresponsive properties of hydrogels are ascribed to the formation of PAA-grafted PNIPAAm networks, in which the water-soluble PAA chains behave as the hydrophiphilic tunnels and allow water molecules to go through and, thus, to accelerate the diffusion of water molecules.

  8. Radiation-induced grafting of diallyldimethylammonium chloride onto acrylic acid grafted polyethylene

    NASA Astrophysics Data System (ADS)

    Francis, Sanju; Dhanawade, B. R.; Mitra, D.; Varshney, Lalit; Sabharwal, Sunil

    2009-01-01

    Diallyldimethylammonium chloride (DADMAC) was grafted onto polyethylene (PE) films by a double grafting procedure. The PE film was initially modified by grafting acrylic acid (AA), through a mutual irradiation method. AA-g-PE film, thus obtained was subjected to subsequent radiation grafting reaction of DADMAC, to give a DADMAC-g-AA-g-PE film having a comb-type structure. The influence of different conditions, such as the extent of AA grafting, DADMAC concentration, absorbed dose and dose rate, on the grafting yield of DADMAC was investigated. A maximum DADMAC grafting of 30% was achieved. The equilibrium degree of swelling (EDS) of the grafted films were gravimetrically determined. TGA and FT-IR techniques were employed to characterize the grafted PE films.

  9. Synthesis, characterization, and morphology study of poly(acrylamide-co-acrylic acid)-grafted-poly(styrene-co-methyl methacrylate) "raspberry"-shape like structure microgels by pre-emulsified semi-batch emulsion polymerization.

    PubMed

    Ramli, Ros Azlinawati; Hashim, Shahrir; Laftah, Waham Ashaier

    2013-02-01

    A novel microgels were polymerized using styrene (St), methyl methacrylate (MMA), acrylamide (AAm), and acrylic acid (AAc) monomers in the presence of N,N'-methylenebisacrylamide (MBA) cross-linker. Pre-emulsified monomer was first prepared followed by polymerizing monomers using semi-batch emulsion polymerization. Fourier Transform Infrared Spectroscopy (FTIR) and (1)H Nuclear Magnetic Resonance (NMR) were used to determine the chemical structure and to indentify the related functional group. Grafting and cross-linking of poly(acrylamide-co-acrilic acid)-grafted-poly(styrene-co-methyl methacrylate) [poly(AAm-co-AAc)-g-poly(St-co-MMA)] microgels are approved by the disappearance of band at 1300 cm(-1), 1200 cm(-1) and 1163 cm(-1) of FTIR spectrum and the appearance of CH peaks at 5.5-5.7 ppm in (1)H NMR spectrum. Scanning Electron Microscope (SEM) images indicated that poly(St-co-MMA) particle was lobed morphology coated by cross-linked poly(AAm-co-AAc) shell. Furthermore, SEM results revealed that poly(AAm-co-AAc)-g-poly(St-co-MMA) is composite particle that consist of "raspberry"-shape like structure core. Internal structures of the microgels showed homogeneous network of pores, an extensive interconnection among pores, thicker pore walls, and open network structures. Water absorbency test indicated that the sample with particle size 0.43 μm had lower equilibrium water content, % than the sample with particle size 7.39 μm.

  10. Electrochemical imprinted sensor for determination of oleanic acid based on poly (sodium 4-styrenesulfonate-co-acrylic acid)-grafted multi-walled carbon nanotubes-chitosan and cobalt hexacyanoferrate nanoparticles.

    PubMed

    Hu, Yufang; Zhang, Zhaohui; Li, Jiaxing; Zhang, Huabin; Luo, Lijuan; Yao, Shouzhuo

    2012-01-15

    A novel sensitive and selective imprinted electrochemical sensor for the determination of oleanic acid was constructed on a carbon electrode by stepwise modification of functional multi-walled carbon nanotubes, cobalt hexacyanoferrate nanoparticles and a thin imprinted sol-gel film. The fabrication of a homogeneous porous poly (sodium 4-styrenesulfonate-co-acrylic acid)-grafted multi-walled carbon nanotubes/SiO(2)-chitosan nanocomposite film was conducted by controllable electrodeposition technology. The surface morphologies of the modified electrodes were characterized by scanning electron microscope. The performance of the imprinted sensor was investigated by cyclic voltammetry, square wave voltammetry and electrochemical impedance spectroscopy in detail. The imprinted sensor displayed high sensitivity and selectivity towards oleanic acid. A linear relationship between the sensor response signal and the logarithm of oleanic acid concentrations ranging from 1.0×10(-8) to 1.0×10(-3) mol L(-1) was obtained with a detection limit of 2.0×10(-9) mol L(-1). It was applied to the determination of oleanic acid in real capsule samples successfully.

  11. Radiation induced deposition of copper nanoparticles inside the nanochannels of poly(acrylic acid)-grafted poly(ethylene terephthalate) track-etched membranes

    NASA Astrophysics Data System (ADS)

    Korolkov, Ilya V.; Güven, Olgun; Mashentseva, Anastassiya A.; Atıcı, Ayse Bakar; Gorin, Yevgeniy G.; Zdorovets, Maxim V.; Taltenov, Abzal A.

    2017-01-01

    Poly(ethylene terephthalate) PET, track-etched membranes (TeMs) with 400 nm average pore size were UV-grafted with poly(acrylic acid) (PAA) after oxidation of inner surfaces by H2O2/UV system. Carboxylate groups of grafted PAA chains were easily complexed with Cu2+ ions in aqueous solutions. These ions were converted into metallic copper nanoparticles (NPs) by radiation-induced reduction of copper ions in aqueous-alcohol solution by gamma rays in the dose range of 46-250 kGy. Copper ions chelating with -COOH groups of PAA chains grafted on PET TeMs form polymer-metal ion complex that prevent the formation of agglomerates during reduction of copper ions to metallic nanoparticles. The detailed analysis by X-Ray diffraction technique (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX) confirmed the deposition of copper nanoparticles with the average size of 70 nm on the inner surface of nanochannels of PET TeMs. Samples were also investigated by FTIR, ESR spectroscopies to follow copper ion reduction.

  12. Conducting polymer films fabricated by oxidative graft copolymerization of aniline on poly(acrylic acid) grafted poly(ethylene terephthalate) surfaces.

    PubMed

    Wang, Jiku; Liu, Xuyan; Choi, Ho-Suk; Kim, Jong-Hoon

    2008-11-27

    A conductive polyaniline/poly(ethylene terephthalate) (PANI/PET) composite film was fabricated via the oxidative graft copolymerization of aniline (ANI) onto the plasma-induced poly(acrylic acid) (PAAc) grafted PET surface. The attenuated total reflectance Fourier transform infrared spectroscopy spectra (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) results confirmed that PANI was successfully grafted onto the surface of the PAAc-g-PET films. The effects of the experimental conditions on the percentage of PANI grafted onto the PAAc-g-PET films were extensively investigated. A very high grafting percentage of ANI can be obtained through the acid-base reaction between the aniline monomer and PAAc on the PAAc-g-PET surface at high temperature. As a result, the grafting percentage of PANI can be increased to as high as 12.18 wt %, which causes the surface resistance of the PANI-g-PAAc-g-PET film to be reduced to about 1000 Omega/sq. We predicted that this is because of the high flexibility of the PAAc molecular chains and high solubility of aniline, both of which facilitate the binding of aniline to PAAc during this high temperature acid-base reaction. It was observed by atomic force microscopy (AFM) that the PANI-modified PET surface exhibits higher size irregularity and surface roughness, which further indicated that a much greater number of aniline molecules can be reactively bonded to and distributed along the grafted AAc chains and that the PANI-g-PAAc-g-PET surface resulting from the sequential oxidative graft copolymerization can possess higher electrical conductivity.

  13. Radiation-induced grafting of acrylic acid onto polypropylene film and its biodegradability

    NASA Astrophysics Data System (ADS)

    Mandal, Dev K.; Bhunia, Haripada; Bajpai, Pramod K.; Chaudhari, C. V.; Dubey, K. A.; Varshney, L.

    2016-06-01

    Polypropylene based commodity polyolefins are widely used in packaging, manufacturing, electrical, pharmaceutical and other applications. The aim of the present work is to study the effect of grafting of acrylic acid on the biodegradability of acrylic acid grafted polypropylene. The effect of different conditions showed that grafting percentage increased with increase in monomer concentration, radiation dose and inhibitor concentration but decreased with increase in radiation dose rate. The maximum grafting of 159.4% could be achieved at optimum conditions. The structure of grafted polypropylene films at different degree of grafting was characterized by EDS, FTIR, TGA, DSC, SEM and XRD. EDS studies showed that the increase in acrylic acid grafting percentage increased the hydrophilicity of the grafted films. FTIR studies indicated the presence of acrylic acid on the surface of polypropylene film. TGA studies revealed that thermal stability decreased with increase in grafting percentage. DSC studies showed that melting temperature and crystallinity of the grafted polypropylene films lower than polypropylene film. SEM studies indicated that increase in acrylic acid grafting percentage increased the wrinkles in the grafted films. The maximum biodegradability could be achieved to 6.85% for 90.5% grafting. This suggested that microorganisms present in the compost could biodegrade acrylic acid grafted polypropylene.

  14. Biosoftening of coir fiber using selected microorganisms.

    PubMed

    Rajan, Akhila; Senan, Resmi C; Pavithran, C; Abraham, T Emilia

    2005-12-01

    Coir fiber belongs to the group of hard structural fibers obtained from coconut husk. As lignin is the main constituent of coir responsible for its stiffness, microbes that selectively remove lignin without loss of appreciable amounts of cellulose are extremely attractive in biosoftening. Five isolated strains were compared with known strains of bacteria and fungi. The raw fiber treated with Pseudomonas putida and Phanerocheate chrysosporium produced better softened fiber at 30+/-2 degrees C and neutral pH. FeSO4 and humic acid were found to be the best inducers for P. chrysosporium and P. putida, respectively, while sucrose and dextrose were the best C-sources for both. Biosoftening of unretted coir fibers was more advantageous than the retted fibers. Unlike the weak chemically softened fiber, microbial treatment produced soft, whiter fibers having better tensile strength and elongation (44.6-44.8%) properties. Scanning electron microscopy photos showed the mycelia penetrating the pores of the fiber, removing the tylose plug and degrading lignin.

  15. Chromium removal from electroplating wastewater by coir pith.

    PubMed

    Suksabye, Parinda; Thiravetyan, Paitip; Nakbanpote, Woranan; Chayabutra, Supanee

    2007-03-22

    Coir pith is a by-product from padding used in mattress factories. It contains a high amount of lignin. Therefore, this study investigated the use of coir pith in the removal of hexavalent chromium from electroplating wastewater by varying the parameters, such as the system pH, contact time, adsorbent dosage, and temperature. The maximum removal (99.99%) was obtained at 2% (w/v) dosage, particle size <75microm, at initial Cr(VI) 1647mgl(-1), system pH 2, and an equilibrium time of 18h. The adsorption isotherm of coir pith fitted reasonably well with the Langmuir model. The maximum Cr(VI) adsorption capacity of coir pith at 15, 30, 45 and 60 degrees C was 138.04, 197.23, 262.89 and 317.65mgCr(VI)g(-1) coir pith, respectively. Thermodynamic parameters indicated an endothermic process and the adsorption process was favored at high temperature. Desorption studies of Cr(VI) on coir pith and X-ray absorption near edge structure (XANES) suggested that most of the chromium bound on the coir pith was in Cr(III) form due to the fact that the toxic Cr(VI) adsorbed on the coir pith by electrostatic attraction was easily reduced to less toxic Cr(III). Fourier transform infrared (FT-IR) spectrometry analysis indicated that the carbonyl (CO) groups and methoxy (O-CH(3)) groups from the lignin structure in coir pith may be involved in the mechanism of chromium adsorption. The reduced Cr(III) on the coir pith surface may be bound with CO groups and O-CH(3) groups through coordinate covalent bonding in which a lone pair of electrons in the oxygen atoms of the methoxy and carbonyl groups can be donated to form a shared bond with Cr(III).

  16. Degradation and compatibility behaviors of poly(glycolic acid) grafted chitosan.

    PubMed

    Zhang, Luzhong; Dou, Sufeng; Li, Yan; Yuan, Ying; Ji, Yawei; Wang, Yaling; Yang, Yumin

    2013-07-01

    The films of poly(glycolic acid) grafted chitosan were prepared without using a catalyst to improve the degradable property of chitosan. The films were characterized by Fourier transform-infrared spectroscopy and X-ray photoelectron spectroscopy (XPS). The degradation of the poly(glycolic acid) grafted chitosan films were investigated in the lysozyme solution. In vitro degradation tests revealed that the degradation rate of poly(glycolic acid) grafted chitosan films increased dramatically compared with chitosan. The degradation rate of poly(glycolic acid) grafted chitosan films gradually increased with the increasing of the molar ratio of glycolic acid to chitosan. Additionally, the poly(glycolic acid) grafted chitosan films have good biocompatibility, as demonstrated by in vitro cytotoxicity of the extraction fluids. The biocompatible and biodegradable poly(glycolic acid) grafted chitosan would be an effective material with controllable degradation rate to meet the diverse needs in biomedical fields.

  17. Use of coir pith particles in composites with Portland cement.

    PubMed

    Brasileiro, Gisela Azevedo Menezes; Vieira, Jhonatas Augusto Rocha; Barreto, Ledjane Silva

    2013-12-15

    Brazil is the fourth largest world's producer of coconut (Cocos nucifera L.). Coconut crops generate several wastes, including, coir pith. Coir pith and short fibers are the byproducts of extracting the long fibers and account for approximately 70% of the mature coconut husk. The main use of coir pith is as an agricultural substrate. Due to its shape and small size (0.075-1.2 mm), this material can be considered as a particulate material. The aim of this study was to evaluate the use of coir pith as an aggregate in cementitious composites and to evaluate the effect of the presence of sand in the performance of these composites. Some composites were produced exclusively with coir pith particles and other composites with coir pith partially substituting the natural sand. The cementitious composites developed were tested for their physical and mechanical properties and characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy to evaluate the effect of coir pith particles addition in cement paste and sand-cement-mortar. The statistical significance of the results was evaluated by one-way analysis of variance (ANOVA) test followed by multiple comparisons of the means by Tukey's test that showed that the composites with coir pith particles, with or without natural sand, had similar mechanical results, i.e., means were not statistically different at 5% significance level. There was a reduction in bulk density and an improved post-cracking behavior in the composites with coir pith particles compared to conventional mortar and to cement paste. These composites can be used for the production of lightweight, nonstructural building materials, according to the values of compressive strength (3.97-4.35 MPa) and low bulk density (0.99-1.26 g/cm(3)).

  18. Experimental study using coir geotextiles in watershed management

    NASA Astrophysics Data System (ADS)

    Vishnudas, S.; Savenije, H. H. G.; van der Zaag, P.; Anil, K. R.; Balan, K.

    2005-11-01

    This paper presents the results of a field experiment conducted in Kerala, South India, to test the effectiveness of coir geotextiles for embankment protection. In the context of sustainable watershed management, coir is a cheap and locally available material that can be used to strengthen traditional earthen bunds or protect the banks of village ponds from erosion. Particularly in developing countries, where coir is abundantly available and textiles can be produced by small-scale industry, this is an attractive alternative for conventional methods.

  19. Cartilage repair with autogenic perichondrium cell and polylactic acid grafts.

    PubMed

    Dounchis, J S; Bae, W C; Chen, A C; Sah, R L; Coutts, R D; Amiel, D

    2000-08-01

    The repair of articular cartilage injuries remains a challenge, with many of the current therapeutic strategies based on the grafting or recruitment of chondrogenic tissues or cells. This 1-year study compared the repair of a 3.7-mm diameter by 3-mm deep osteochondral defect in the medial femoral condyle of 24 New Zealand White rabbits; the defect was obtained using an autogenic perichondrium cell polylactic acid composite graft with a contralateral control in which the osteochondral defect remained empty. To elucidate the effect of host immune responses on the repair process after perichondrium cell transplantation, the results of the autogenic perichondrium cell polylactic acid graft group were compared with those obtained in the authors' previous 1-year study of allogenic perichondrium cell polylactic acid composite grafts implanted in a similar model. One year after surgery, the repair site underwent gross inspection and histologic, histomorphometric, biochemical, and biomechanical analyses. The autogenic perichondrium cell polylactic acid graft group (92%) and the control group in which the osteochondral defect remained empty (88%) resulted in a high percentage of grossly acceptable repairs. The autogenic grafts appeared to augment the intrinsic healing capacity of the animals (as compared with the animals in the No Implant Group). The autogenic perichondrium cell polylactic and grafts improved the histologic appearance and percentage of Type II collagen of the cartilaginous repair tissue. Compared with allogenic grafts, the autogenic grafts had better reconstitution of the subchondral bone. However, the results of this experimental model suggest a suboptimal concentration of glycosaminoglycans in the neocartilage matrix, a depressed surface of the repair tissue, a histologic appearance that was not equivalent to that of normal articular cartilage, and reduced biomechanical properties for the repair tissue. The future application of growth factors to this

  20. A clinical and radiographic study of coir workers.

    PubMed Central

    Uragoda, C G

    1975-01-01

    Processing of coir, which is the fibre obtained from the husk of the coconut, is a dusty procedure; 779 workers in two coir processing factories in Sri Lanka were examined clincally and radiographically for evidence of respiratory disease. Respiratory symptoms were present in 20 (2-6%) of them, which is no higher than in the general population. Respiratory disease such as asthma, chronic bronchitis, byssinosis, and pulmonary tuberculosis which may occur from occupational exposures were considered, but there was no evidence to suggest a definite association between these conditions and coir dust. Twenty-two workers had abnormal chest radiographs, but when compared with a control group of 591 workers from an engineering firm where lesions were found in 20 cases, there was no significant difference. In the opinion of the medical officer, management and workers of the large factory investigated, coir dust does not produce any respiratory disability. The chemical composition of coir dust is similar to that of sisal which is also relatively inert. PMID:1125129

  1. Mechanism of Cr(VI) adsorption by coir pith studied by ESR and adsorption kinetic.

    PubMed

    Suksabye, Parinda; Nakajima, Akira; Thiravetyan, Paitip; Baba, Yoshinari; Nakbanpote, Woranan

    2009-01-30

    The oxidation state of chromium in coir pith after Cr(VI) adsorption from aqueous solution was investigated using electron spin resonance (ESR). To elucidate the mechanism of chromium adsorption on coir pith, the adsorption studies of Cr(VI) onto lignin, alpha-cellulose and holocellulose extracted from coir pith were also studied. ESR signals of Cr(V) and Cr(III) were observed in coir pith adsorbed Cr(VI) at solution pH 2, while ESR spectra of lignin extracted from coir pith revealed only the Cr(III) signal. In addition, ESR signal of Cr(V) was observed in alpha-cellulose and holocellulose extracted from coir pith adsorbed Cr(VI). These results confirmed that lignin in coir pith reduced Cr(VI) to Cr(III) while alpha-cellulose and holocellulose extracted from coir pith reduced Cr(VI) to Cr(V). The Cr(V) signal exhibited in ESR of alpha-cellulose and holocellulose might be bound with glucose in cellulose part of coir pith. In addition, xylose which is main in pentosan part of coir pith, indicated that it is involved in form complex with Cr(V) on coir pith. The adsorption kinetic of Cr(VI) from aqueous solution on coir pith was also investigated and described well with pseudo second order model. ESR and desorption experiments confirmed that Cr(VI), Cr(V) and Cr(III), exist in coir pith after Cr(VI) adsorption. The desorption data indicated that the percentage of Cr(VI), Cr(V) and Cr(III) in coir pith were 15.63%, 12.89% and 71.48%, respectively.

  2. Radiation grafting of acrylic and methacrylic acid to cellulose fibers to impart high water sorbency

    SciTech Connect

    Zahran, A.H.; Williams, J.L.; Stannett, V.T.

    1980-04-01

    Acrylic and methacrylic acids have been directly grafted to rayon and cotton using the preirradiation technique with /sup 60/ Co gamma rays. The rate of grafting increased with increasing temperature and monomer concentration, as did the final degree of grafting. The amount and rate of grafting also increased with the total irradiation dose but tended to level off at higher doses, in agreement with the leveling off of the radical content reported previously. Methacrylic acid grafted more and faster than acrylic acid to both rayon and cotton. Methacrylic acid grafted more with rayon than cotton, but acrylic acid gave somewhat similar yields with both fibers. The water abosrbency of the grafted fibers depended strongly on their posttreatment. Decrystallizing with 70% zinc chloride or with hot sodium hydroxidy developed supersorbency. The two treatments in succession, respectively, gave the highest values. Metacrylic acid brought about less sorbency than the corrsponding acrylic acid grafts. Useful levels of grafting and supersorbency could be readily and practically achieved by the methods described.

  3. Methyl acrylate

    Integrated Risk Information System (IRIS)

    Methyl acrylate ; CASRN 96 - 33 - 3 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Ef

  4. Acrylic acid

    Integrated Risk Information System (IRIS)

    Acrylic acid ( CASRN 79 - 10 - 7 ) Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Eff

  5. Physico-mechanical properties of chemically treated palm and coir fiber reinforced polypropylene composites.

    PubMed

    Haque, Md Mominul; Hasan, Mahbub; Islam, Md Saiful; Ali, Md Ershad

    2009-10-01

    In this work, palm and coir fiber reinforced polypropylene bio-composites were manufactured using a single extruder and injection molding machine. Raw palm and coir were chemically treated with benzene diazonium salt to increase their compatibility with the polypropylene matrix. Both raw and treated palm and coir fiber at five level of fiber loading (15, 20, 25, 30 and 35 wt.%) was utilized during composite manufacturing. Microstructural analysis and mechanical tests were conducted. Comparison has been made between the properties of the palm and coir fiber composites. Treated fiber reinforced specimens yielded better mechanical properties compared to the raw composites, while coir fiber composites had better mechanical properties than palm fiber ones. Based on fiber loading, 30% fiber reinforced composites had the optimum set of mechanical properties.

  6. The Use of Arbuscular Mycorrhizal Fungi to Improve Strawberry Production in Coir Substrate

    PubMed Central

    Robinson Boyer, Louisa; Feng, Wei; Gulbis, Natallia; Hajdu, Klara; Harrison, Richard J.; Jeffries, Peter; Xu, Xiangming

    2016-01-01

    Strawberry is an important fruit crop within the UK. To reduce the impact of soil-borne diseases and extend the production season, more than half of the UK strawberry production is now in substrate (predominantly coir) under protection. Substrates such as coir are usually depleted of microbes including arbuscular mycorrhizal fungi (AMF) and consequently the introduction of beneficial microbes is likely to benefit commercial cropping systems. Inoculating strawberry plants in substrate other than coir has been shown to increase plants tolerance to soil-borne pathogens and water stress. We carried out studies to investigate whether AMF could improve strawberry production in coir under low nitrogen input and regulated deficit irrigation. Application of AMF led to an appreciable increase in the size and number of class I fruit, especially under either deficient irrigation or low nitrogen input condition. However, root length colonization by AMF was reduced in strawberry grown in coir compared to soil and Terragreen. Furthermore, the appearance of AMF colonizing strawberry and maize roots grown in coir showed some physical differences from the structure in colonized roots in soil and Terragreen: the colonization structure appeared to be more compact and smaller in coir. PMID:27594859

  7. Mechanical characterization of coir/palmyra waste fiber hybrid composites

    NASA Astrophysics Data System (ADS)

    Arumugaprabu, V.; Uthayakumar, M.; Cardona, F.; Sultan, M. T. H.

    2016-10-01

    In the present days, the utilization of palmyra fiber in automotive and aerospace applications has increased drastically due to its high strength and low weight. This research focuses on the development of composite materials using palmyra waste and coir fiber with polyester as a matrix. The mechanical properties such as tensile, flexural and impact strength of composites were investigated. Palmyra waste fiber and coir fiber with relative varying weight percentage in the ratio of 50:50, 40:60, 30:70 and 20:80 had been considered for the study. The composites were prepared by the compression moulding method. In addition, the prepared composites were subjected to moisture studies for 24 hours, 48 hours and 72 hours to know the composite resistance to water absorption. The results showed an increase in all the mechanical properties from the addition of palmyra waste. After analysing the results obtained from the study, a suitable application in the automobile and aerospace industries is suggested for the new developed composite.

  8. The protective and attractive covering of a vegetated embankment using coir geotextiles

    NASA Astrophysics Data System (ADS)

    Vishnudas, S.; Savenije, H. H. G.; van der Zaag, P.; Anil, K. R.; Balan, K.

    2006-08-01

    This paper presents the results of a field experiment conducted in Kerala, South India, to test the effectiveness of coir geotextiles for embankment protection. The results reveal that treatment with geotextile in combination with grass is an effective eco-hydrological measure to protect steep slopes from erosion. In the context of sustainable watershed management, coir is a cheap and locally available material that can be used to strengthen traditional earthen bunds or protect the banks of village ponds from erosion. Particularly in developing countries, where coir is abundantly available and textiles can be produced by small-scale industry, this is an attractive alternative for conventional methods. This paper analyses the performance of coir geotextile in different treatments with respect to soil moisture content, protection against erosion and biomass production.

  9. Median and common peroneal neuropathy in coir workers of Alappuzha district, Kerala

    PubMed Central

    Chandra, Sadanandavalli Retnaswami; Anand, Biji; Issac, Thomas Gregor

    2017-01-01

    Introduction: Coir work, in a large number of people involves mechanically rolling the coconut fibers into coir which is later subjected to various processes. The primary work is done as a cottage industry specially by women in the sitting posture for several hours. This study reports evidence of median and common peroneal neuropathy electrophysiologically in people who had been engaged in this job for several years. This study was initiated to establish the possible relationship between coir work and symptomatic neuropathies which was seen in that region with all investigations “for other causes not” contributing to the etiological diagnosis. Subjects and Methods: One hundred and forty-two upper limbs and 142 lower limbs in patients engaged in long years of coir work but having no symptoms were evaluated electrophysiologically with informed consent and financial compensation, appropriate inclusion and exclusion criteria were followed as described in the text. Results: There is electrophysiological evidence for median and common peroneal neuropathy in persons engaged in long years of coir work. Conclusions: Coir workers neuropathy appears to be a new occupational neuropathy which can be prevented by following simple preventive measures. PMID:28298838

  10. Drying kinetics and mathematical modeling of hot air drying of coconut coir pith.

    PubMed

    Fernando, J A K M; Amarasinghe, A D U S

    2016-01-01

    Drying kinetics of coir pith was studied and the properties of compressed coir pith discs were analyzed. Coir pith particles were oven dried in the range of temperatures from 100 to 240 °C and the rehydration ability of compressed coir pith was evaluated by finding the volume expansion. The optimum drying temperature was found to be 140 °C. Hot air drying was carried out to examine the drying kinetics by allowing the coir pith particles to fluidize and circulate inside the drying chamber. Particle motion within the drying chamber closely resembled the particle motion in a flash dryer. The effective moisture diffusivity was found to increase from 1.18 × 10(-8) to 1.37 × 10(-8) m(2)/s with the increase of air velocity from 1.4 to 2.5 m/s respectively. Correlation analysis and residual plots were used to determine the adequacy of existing mathematical models for describing the drying behavior of coir pith. The empirical models, Wang and Singh model and Linear model, were found to be adequate for accurate prediction of drying behavior of coir pith. A new model was proposed by modifying the Wang and Singh model and considering the effect of air velocity. It gave the best correlation between observed and predicted moisture ratio with high value of coefficient of determination (R(2)) and lower values of root mean square error, reduced Chi square (χ(2)) and mean relative deviation (E%).

  11. Acrylate Systemic Contact Dermatitis.

    PubMed

    Sauder, Maxwell B; Pratt, Melanie D

    2015-01-01

    Acrylates, the 2012 American Contact Dermatitis Society allergen of the year, are found in a range of products including the absorbent materials within feminine hygiene pads. When fully polymerized, acrylates are nonimmunogenic; however, if not completely cured, the monomers can be potent allergens.A 28-year-old woman is presented, who had her teeth varnished with Isodan (Septodont, Saint-Maur-des-Fossés, France) containing HEMA (2-hydroxyethyl methacrylate) with no initial reaction. Approximately 1 month later, the patient developed a genital dermatitis secondary to her feminine hygiene pads. The initial reaction resolved, but 5 months later, the patient developed a systemic contact dermatitis after receiving a second varnishing.The patient was dramatically patch test positive to many acrylates. This case demonstrates a reaction to likely unpolymerized acrylates within a feminine hygiene pad, as well as broad cross-reactivity or cosensitivity to acrylates, and possibly a systemic contact dermatitis with systemic re-exposure to unpolymerized acrylates.

  12. Silicone/Acrylate Copolymers

    NASA Technical Reports Server (NTRS)

    Dennis, W. E.

    1982-01-01

    Two-step process forms silicone/acrylate copolymers. Resulting acrylate functional fluid is reacted with other ingredients to produce copolymer. Films of polymer were formed by simply pouring or spraying mixture and allowing solvent to evaporate. Films showed good weatherability. Durable, clear polymer films protect photovoltaic cells.

  13. Mechanical Properties of Sisal/Coir Fiber Reinforced Hybrid Composites Fabricated by Cold Pressing Method

    NASA Astrophysics Data System (ADS)

    Akash; Sreenivasa Rao, K. V.; Venkatesha Gupta, N. S.; kumar, D. S. Arun

    2016-09-01

    Bio-composites have less density and are environmental friendly materials that require less energy during production and subsequent machining. This paper reports the mechanical and water absorption properties of sodium hydroxide (NaOH) treated sisal and coir fiber reinforced epoxy resin thermo set hybrid composites. The hybrid composites were prepared by traditional cold pressing method at room temperature with applied pressure of 410.4 kg/cm2 for 3 hours pressurization time. The mechanical properties were characterized according to ASTM standards. Hybrid composites with 40wt% of sisal and coir fiber were found to possess higher tensile strength of 48.2MPa and flexural strength of 76.68 MPa among the fabricated hybrid composite specimens. Absorption of water increases with increasing fiber volume. The experimental result also show that the sisal and coir fibers are promising reinforcement for use in low cost bio-composites which have high strength to weight ratio.

  14. Mechanistic studies on the binding of Acid Yellow 99 on coir pith.

    PubMed

    Khan, Md Motiar R; Ray, Manju; Guha, Arun K

    2011-02-01

    The interaction of Acid Yellow 99 (AY 99) with coir pith has been investigated in aqueous medium to understand the mechanism of adsorption and explore the potentiality of this biomass towards controlling pollution resulting from textile dyes. The obtained results establish that one gram of coir pith can adsorb 442.13 mg of AY 99. The adsorption process is found to be a function of pH of the solution, the optimum pH value being 2.0. The process follows Langmuir-Freundlich dual isotherm model. Scanning electron microscopic analysis demonstrates that on dye adsorption the biomass develops uneven and irregular surface. X-ray diffraction study indicates incorporation of the dye into the micropores and macropores of the adsorbent and thereby enhancing its degree of crystallinity. The results of Fourier transform infrared (FTIR) spectroscopy and chemical modification of the functional groups establish that binding of AY 99 on coir pith occurs through electrostatic and complexation reaction.

  15. Kinetic study of enzymatic hydrolysis of acid-pretreated coconut coir

    NASA Astrophysics Data System (ADS)

    Fatmawati, Akbarningrum; Agustriyanto, Rudy

    2015-12-01

    Biomass waste utilization for biofuel production such as bioethanol, has become more prominent currently. Coconut coir is one of lignocellulosic food wastes, which is abundant in Indonesia. Bioethanol production from such materials consists of more than one step. Pretreatment and enzymatic hydrolysis is crucial steps to produce sugar which can then be fermented into bioethanol. In this research, ground coconut coir was pretreated using dilute sulfuric acid at 121°C. This pretreatment had increased the cellulose content and decreased the lignin content of coconut coir. The pretreated coconut coir was hydrolyzed using a mix of two commercial cellulase enzymes at pH of 4.8 and temperature of 50°C. The enzymatic hydrolysis was conducted at several initial coconut coir slurry concentrations (0.1-2 g/100 mL) and reaction times (2-72 hours). The reducing sugar concentration profiles had been produced and can be used to obtain reaction rates. The highest reducing sugar concentration obtained was 1,152.567 mg/L, which was produced at initial slurry concentration of 2 g/100 mL and 72 hours reaction time. In this paper, the reducing sugar concentrations were empirically modeled as a function of reaction time using power equations. Michaelis-Menten kinetic model for enzymatic hydrolysis reaction is adopted. The kinetic parameters of that model for sulfuric acid-pretreated coconut coir enzymatic hydrolysis had been obtained which are Vm of 3.587×104 mg/L.h, and KM of 130.6 mg/L.

  16. Synthesis of a novel acrylated abietic acid-g-bacterial cellulose hydrogel by gamma irradiation.

    PubMed

    Abeer, Muhammad Mustafa; Amin, Mohd Cairul Iqbal Mohd; Lazim, Azwan Mat; Pandey, Manisha; Martin, Claire

    2014-09-22

    Acrylated abietic acid (acrylated AbA) and acrylated abietic acid-grafted bacterial cellulose pH sensitive hydrogel (acrylated AbA-g-BC) were prepared by a one-pot synthesis. The successful dimerization of acrylic acid (AA) and abietic acid (AbA) and grafting of the dimer onto bacterial cellulose (BC) was confirmed by 13C solid state NMR as well as FT-IR. X-ray diffraction analysis showed characteristic peaks for AbA and BC; further, there was no effect of increasing amorphous AA content on the overall crystallinity of the hydrogel. Differential scanning calorimetry revealed a glass transition temperature of 80°C. Gel fraction and swelling studies gave insight into the features of the hydrogel, suggesting that it was suitable for future applications such as drug delivery. Scanning electron microscopy observations showed an interesting interpenetrating network within the walls of hydrogel samples with the lowest levels of AA and gamma radiation doses. Cell viability test revealed that the synthesized hydrogel is safe for future use in biomedical applications.

  17. Effect of aniline on cadmium adsorption by sulfanilic acid-grafted magnetic graphene oxide sheets.

    PubMed

    Hu, Xin-jiang; Liu, Yun-guo; Zeng, Guang-ming; Wang, Hui; Hu, Xi; Chen, An-wei; Wang, Ya-qin; Guo, Yi-Mming; Li, Ting-ting; Zhou, Lu; Liu, Shao-heng; Zeng, Xiao-xia

    2014-07-15

    Cd(II) has posed severe health risks worldwide. To remove this contaminant from aqueous solution, the sulfanilic acid-grafted magnetic graphene oxide sheets (MGOs/SA) were prepared and characterized. The mutual effects of Cd(II) and aniline adsorption on MGOs/SA were studied. The effects of operating parameters such as pH, ionic strength, contact time and temperature on the Cd(II) enrichment, as well as the adsorption kinetics and isotherm were also investigated. The results demonstrated that MGOs/SA could effectively remove Cd(II) and aniline from the aqueous solution and the two adsorption processes were strongly dependent on solution pH. The Cd(II) adsorption was reduced by the presence of aniline at pH<5.4 but was improved at pH>5.4. The presence of Cd(II) diminished the adsorption capacity for aniline at pH<7.8 but enhanced the aniline adsorption at pH>7.8. The decontamination of Cd(II) by MGOs/SA was influenced by ionic strength. Besides, the adsorption process could be well described by pseudo-second-order kinetic model. The intraparticle diffusion study revealed that the intraparticle diffusion was not the only rate-limiting step for the adsorption process. Moreover, the experimental data of isotherm followed the Freundlich isotherm model.

  18. Effect of Protocatechuic Acid-Grafted-Chitosan Coating on the Postharvest Quality of Pleurotus eryngii.

    PubMed

    Liu, Jun; Meng, Chen-Guang; Wang, Xing-Chi; Chen, Yao; Kan, Juan; Jin, Chang-Hai

    2016-09-28

    Protocatechuic acid-grafted-chitosan (PA-g-CS) solution with antioxidant activity was developed as a novel edible coating material for Pleurotus eryngii postharvest storage. The effect of PA-g-CS coating on the postharvest quality of P. eryngii was investigated by determination of various physicochemical parameters and enzyme activities. Results showed that the antioxidant capacity and viscosity of PA-g-CS solutions were closely related to the grafting degree and were much higher than that of chitosan (CS) solution. At the end of 15 days of storage, serious mushroom browning was observed in the control and CS coating groups. By contrast, PA-g-CS coating groups with medium and high grafting degrees maintained better physical appearance. Among all of the treatment groups, P. eryngii in PA-g-CS III coating group exhibited the highest firmness and the lowest weight loss, browning degree, respiration rate, malondialdehyde content, electrolyte leakage rate, superoxide anion production rate, and hydrogen peroxide content. Moreover, P. eryngii in PA-g-CS III coating group maintained relatively higher antioxidant enzyme activities but lower polyphenol oxidase activity than other treatment groups. Therefore, PA-g-CS III is a promising preservation agent for P. eryngii.

  19. Immobilization of anaerobic bacteria on rubberized-coir for psychrophilic digestion of night soil.

    PubMed

    Dhaked, Ram Kumar; Ramana, Karna Venkat; Tomar, Arvind; Waghmare, Chandrakant; Kamboj, Dev Vrat; Singh, Lokendra

    2005-08-01

    Low-ambient temperatures, <30 degrees C, are known to cause drastic reduction in the efficiency of anaerobic biodigesters due to low-growth rate of the constituent bacterial consortium. Immobilization of anaerobic bacteria has been attempted in the biodigester operating at 10 degrees C. Various matrices were screened and evaluated for the immobilization of bacteria in digesters. Anaerobic digestion of night soil was carried out with hydraulic retention time in the range of 9-18 days. Among the tested matrices, rubberized-coir was found to be the most useful at 10 degrees C with optimum hydraulic retention time of 15 days. Optimum amount of coir was found as 25 g/L of the working volume of biodigesters. Immobilization of bacteria on the coir was observed by scanning electron microscopy and fluorescent microscopy. The study indicates that rubberized-coir can be utilized to increase biodegradation of night soil at higher organic loading. Another advantage of using this matrix is that it is renewable and easily available in comparison to other synthetic polymeric matrices.

  20. Structural characterization of lignin isolated from coconut (Cocos nucifera) coir fibers.

    PubMed

    Rencoret, Jorge; Ralph, John; Marques, Gisela; Gutiérrez, Ana; Martínez, Ángel T; del Río, José C

    2013-03-13

    The structure of the isolated milled "wood" lignin from coconut coir has been characterized using different analytical methods, including Py-GC/MS, 2D NMR, DFRC, and thioacidolysis. The analyses demonstrated that it is a p-hydroxyphenyl-guaiacyl-syringyl (H-G-S) lignin, with a predominance of G units (S/G ratio 0.23) and considerable amounts of associated p-hydroxybenzoates. Two-dimensional NMR indicated that the main substructures present in this lignin include β-O-4' alkyl aryl ethers followed by phenylcoumarans and resinols. Two-dimensional NMR spectra also indicated that coir lignin is partially acylated at the γ-carbon of the side chain with p-hydroxybenzoates and acetates. DFRC analysis showed that acetates preferentially acylate the γ-OH in S rather than in G units. Despite coir lignin's being highly enriched in G-units, thioacidolysis indicated that β-β' resinol structures are mostly derived from sinapyl alcohol. Finally, we find evidence that the flavone tricin is incorporated into the coconut coir lignin, as has been recently noted for various grasses.

  1. Column study of chromium(VI) adsorption from electroplating industry by coconut coir pith.

    PubMed

    Suksabye, Parinda; Thiravetyan, Paitip; Nakbanpote, Woranan

    2008-12-15

    The removal of Cr(VI) from electroplating wastewater by coir pith was investigated in a fixed-bed column. The experiments were conducted to study the effect of important parameters such as bed depth (40-60cm) and flow rate (10-30ml min(-1)). At 0.05 C(t)/C(0), the breakthrough volume increased as flow rate decreased or a bed depth increased due to an increase in empty bed contact time (EBCT). The bed depth service time model (BDST) fit well with the experimental data in the initial region of the breakthrough curve, while the simulation of the whole curve using non-linear regression analysis was effective using the Thomas model. The adsorption capacity estimated from the BDST model was reduced with increasing flow rate, which was 16.40mg cm(-3) or 137.91mg Cr(VI)g(-1) coir pith for the flow rates of 10ml min(-1) and 14.05mg cm(-3) or 118.20mg Cr(VI)g(-1) coir pith for the flow rates of 30ml min(-1). At the highest bed depth (60cm) and the lowest flow rate (10mlmin(-1)), the maximum adsorption reached 201.47mg Cr(VI)g(-1) adsorbent according to the Thomas model. The column was regenerated by eluting chromium using 2M HNO(3) after adsorption studies. The desorption of Cr(III) in each of three cycles was about 67-70%. The desorption of Cr(III) in each cycle did not reach 100% due to the fact that Cr(V) was present through the reduction of Cr(VI), and was still in coir pith, possibly bound to glucose in the cellulose part of coir pith. Therefore, the Cr(V) complex cannot be desorbed in solution. The evidence of Cr(V) signal was observed in coir pith, alpha-cellulose and holocellulose extracted from coir pith using electron spin resonance (ESR).

  2. Properties of polyurethane foam/coconut coir fiber as a core material and as a sandwich composites component

    NASA Astrophysics Data System (ADS)

    Azmi, M. A.; Abdullah, H. Z.; Idris, M. I.

    2013-12-01

    This research focuses on the fabrication and characterization of sandwich composite panels using glass fiber composite skin and polyurethane foam reinforced coconut coir fiber core. The main objectives are to characterize the physical and mechanical properties and to elucidate the effect of coconut coir fibers in polyurethane foam cores and sandwich composite panels. Coconut coir fibers were used as reinforcement in polyurethane foams in which later were applied as the core in sandwich composites ranged from 5 wt% to 20 wt%. The physical and mechanical properties found to be significant at 5 wt% coconut coir fiber in polyurethane foam cores as well as in sandwich composites. It was found that composites properties serve better in sandwich composites construction.

  3. Acrylic vessel cleaning tests

    SciTech Connect

    Earle, D.; Hahn, R.L.; Boger, J.; Bonvin, E.

    1997-02-26

    The acrylic vessel as constructed is dirty. The dirt includes blue tape, Al tape, grease pencil, gemak, the glue or residue form these tapes, finger prints and dust of an unknown composition but probably mostly acrylic dust. This dirt has to be removed and once removed, the vessel has to be kept clean or at least to be easily cleanable at some future stage when access becomes much more difficult. The authors report on the results of a series of tests designed: (a) to prepare typical dirty samples of acrylic; (b) to remove dirt stuck to the acrylic surface; and (c) to measure the optical quality and Th concentration after cleaning. Specifications of the vessel call for very low levels of Th which could come from tape residues, the grease pencil, or other sources of dirt. This report does not address the concerns of how to keep the vessel clean after an initial cleaning and during the removal of the scaffolding. Alconox is recommended as the cleaner of choice. This acrylic vessel will be used in the Sudbury Neutrino Observatory.

  4. Biocompatibility and functional performance of a polyethylene glycol acid-grafted cellulosic membrane for hemodialysis.

    PubMed

    Sirolli, V; Di Stante, S; Stuard, S; Di Liberato, L; Amoroso, L; Cappelli, P; Bonomini, M

    2000-06-01

    In order to improve the biochemical reactivity of the cellulose polymer, which is mainly attributed to the presence of surface hydroxyl groups, derivatized cellulosic membranes have been engineered replacing or masking some or all of the hydroxyl groups in the manufacturing process of the membrane. The present study was set up to analyze both biocompatibility and functional performance of two different derivatized cellulosic membranes (cellulose diacetate; polyethylene glycol, PEG, acid-grafted cellulose) as compared to a synthetic membrane (polymethylmethacrylate, PMMA). Cellulose diacetate is prepared by substituting hydroxyl groups with acetyl groups; PEG cellulose is obtained by grafting PEG chains onto the cellulosic polymer with a smaller amount of substitution than cellulose diacetate. While the three dialyzers provided similar urea and creatinine removal, the dialyzer containing cellulose diacetate showed a reduced ability to remove 32-microglobulin compared to that containing PEG cellulose or PMMA. A transient reduction in leukocyte count was observed for both derivatized cellulosic membranes. The neutrophil and monocyte counts throughout the entire dialysis session showed a closer parallelism with the cellular expression of the adhesive receptor CD 15s (sialyl-Lewis x molecule) than with CD11b/CD18 expression. Platelet activation, as indicated by the percentage of cells expressing the activation markers CD62P (P-selectin) and CD63 (gp53), occurred with all membranes at 15 min of dialysis and also with PMMA at 30 min. An increased formation of platelet-neutrophil and platelet-monocyte coaggregates was found at 15 and 30 min during dialysis with cellulose diacetate and PMMA but not with PEG cellulose. Generally in concomitance with the increase in platelet-neutrophil coaggregates, an increased hydrogen peroxide production by neutrophils occurred. Our results indicate that derivatizing cellulose may represent a useful approach to improve the biocompatibility

  5. Acrylic mechanical bond tests

    SciTech Connect

    Wouters, J.M.; Doe, P.J.

    1991-02-01

    The tensile strength of bonded acrylic is tested as a function of bond joint thickness. 0.125 in. thick bond joints were found to posses the maximum strength while the acceptable range of joints varied from 0.063 in. to almost 0.25 in. Such joints are used in the Sudbury Neutrino Observatory.

  6. Experimental and kinetic studies on methylene blue adsorption by coir pith carbon.

    PubMed

    Kavitha, D; Namasivayam, C

    2007-01-01

    Varying the parameters such as agitation time, dye concentration, adsorbent dose, pH and temperature carried out the potential feasibility of thermally activated coir pith carbon prepared from coconut husk for removal of methylene blue. Greater percentage of dye was removed with decrease in the initial concentration of dye and increase in amount of adsorbent used. Kinetic study showed that the adsorption of dye on coir pith carbon was a gradual process. Lagergren first-order, second-order, intra particle diffusion model and Bangham were used to fit the experimental data. Equilibrium isotherms were analysed by Langmuir, Freundlich, Dubnin-Radushkevich, and Tempkin isotherm. The adsorption capacity was found to be 5.87 mg/g by Langmuir isotherm for the particle size 250-500 microm. The equilibrium time was found to be 30 and 60 min for 10 and 20 mg/L and 100 min for 30, 40 mg/L dye concentrations, respectively. A maximum removal of 97% was obtained at natural pH 6.9 for an adsorbent dose of 100 mg/50 mL and 100% removal was obtained for an adsorbent dose of 600 mg/50 mL of 10 mg/L dye concentration. The pH effect and desorption studies suggest that chemisorption might be the major mode of the adsorption process. The change in entropy (DeltaS0) and heat of adsorption (DeltaH0) of coir pith carbon was estimated as 117.20 J/mol/K and 30.88 kJ/mol, respectively. The high negative value of change in Gibbs free energy indicates the feasible and spontaneous adsorption of methylene blue on coir pith carbon.

  7. Mechanical, thermal, and biodegradable properties of polylactic acid (PLA)/coir fibre biocomposites

    NASA Astrophysics Data System (ADS)

    Dong, Y.; Ghataura, A.; Haroosh, H. J.

    2013-08-01

    Polylactic acid (PLA)/coir fibre biocomposites were fabricated using a compression moulding technique. The effects of fibre content (5-30 wt%) and fibre treatment on mechanical, thermal and biodegradable properties of biocomposites were holistically investigated via mechanical testing, scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and soil burial method to understand the applicability of manufacturing eco-efficient and sustainable "green composites".

  8. Esterified coir pith as an adsorbent for the removal of Co(II) from aqueous solution.

    PubMed

    Parab, Harshala; Joshi, Shreeram; Shenoy, Niyoti; Lali, Arvind; Sarma, U S; Sudersanan, M

    2008-04-01

    Coir pith was chemically modified for the adsorption of cobalt(II) ions from aqueous solution. Chemical modification was done by esterification using succinic anhydride followed by activation with NaHCO(3) in order to improve the adsorption of Co(II). Adsorptive removal of Co(II) from aqueous solution onto modified coir pith was evaluated in batch studies under varying conditions of agitation time and metal ion concentration to assess the kinetic and equilibrium parameters. A pseudo-second-order kinetic model fitted well for the sorption of Co(II) onto modified coir pith. Sorption kinetics showed that the loading of Co(II) by this material was quite fast under ambient conditions. The Langmuir and Freundlich equilibrium isotherm models provided excellent fits for the adsorption data, with R(2) of 0.99 and 0.98, respectively. After esterification, the maximum Co(II) sorption loading Q(0); was greatly improved. It is evident that chemically modified adsorbent exhibits better Co(II) removal capability than raw adsorbent suggesting that surface modification of the adsorbent generates more adsorption sites on its solid surface for metal adsorption. A complete recovery of the adsorbed metal ions from the spent adsorbent was achieved by using 1.0N HCl.

  9. Uranium removal from aqueous solution by coir pith: equilibrium and kinetic studies.

    PubMed

    Parab, Harshala; Joshi, Shreeram; Shenoy, Niyoti; Verma, Rakesh; Lali, Arvind; Sudersanan, M

    2005-07-01

    Basic aspects of uranium adsorption by coir pith have been investigated by batch equilibration. The influence of different experimental parameters such as final solution pH, adsorbent dosage, sorption time, temperature and various concentrations of uranium on uptake were evaluated. Maximum uranium adsorption was observed in the pH range 4.0-6.0. The Freundlich and Langmuir adsorption models were used for the mathematical description of the adsorption equilibrium. The equilibrium data fitted well to both the equilibrium models in the studied concentration range of uranium (200-800 mg/l) and temperatures (305-336 K). The coir pith exhibited the highest uptake capacity for uranium at 317 K, at the final solution pH value of 4.3 and at the initial uranium concentration of 800 mg/l. The kinetics of the adsorption process followed a second-order adsorption. The adsorbent used proved to be suitable for removal of uranium from aqueous solutions. 0.2 N HCl was effective in uranium desorption. The results indicated that the naturally abundant coir pith of otherwise nuisance value exhibited considerable potential for application in removal of uranium from aqueous solution.

  10. Removal of phosphate from aqueous solutions and sewage using natural and surface modified coir pith.

    PubMed

    Krishnan, K Anoop; Haridas, Ajit

    2008-04-01

    Iron impregnated coir pith (CP-Fe-I) can be effectively used for the removal of phosphate from aqueous streams and sewage. Iron impregnation on natural coir pith was carried out by drop by drop addition method. The effect of various factors such as pH, initial concentration of phosphate, contact time and adsorbent dose on phosphate adsorption was studied by batch technique. The pH at 3.0 favored the maximum adsorption of phosphate from aqueous solutions. The effect of pH on phosphate adsorption was explained by pH(zpc), phosphate speciation in solution and affinity of anions towards the adsorbent sites. A comparative study of the adsorption of phosphate using CP-Fe-I and CP (coir pith) was made and results show that the former one is five to six times more effective than the latter. Kinetic studies revealed that the adsorption process followed a pseudo-second order kinetic model. Adsorption followed Langmuir isotherm model. Column studies were conducted to examine the utility of the investigated adsorbent for the removal of phosphate from continuously flowing aqueous solutions.

  11. Investigations of plasma induced effects on the surface properties of lignocellulosic natural coir fibres

    NASA Astrophysics Data System (ADS)

    Praveen, K. M.; Thomas, Sabu; Grohens, Yves; Mozetič, Miran; Junkar, Ita; Primc, Gregor; Gorjanc, Marija

    2016-04-01

    The development of lignocellulosic natural-fibre-reinforced polymers composites are constrained by two limitations: the upper temperature at which the fibre can be processed and the significant differences between the surface energy of the fibre and the polymer matrix. Since the fibres and matrices are chemically different, strong adhesion at their interface is needed for the effective transfer of stress and bond distribution throughout the interface. The present study investigated the plasma induced effects on the surface properties of natural coir fibres. Weakly ionized oxygen plasma was created in two different discharge chambers by an inductively coupled radiofrequency (RF) discharge. The water absorption studies showed an increase of water sorption from 39% to 100%. The morphological study using scanning electron microscopy (SEM) analysis also confirmed the surface changes which were observed after the plasma treatment. The topographic measurements and phase imaging done using atomic force microscopy (AFM) indicated difference in topographic features and etching of coir wall, which points to the removal of the first layer of coir fibre. X-ray photoelectron spectroscopy (XPS) analysis revealed that the oxygen content measured for samples treated at 50 Pa increased from initial 18% to about 32%.

  12. Recycling of agricultural solid waste, coir pith: removal of anions, heavy metals, organics and dyes from water by adsorption onto ZnCl2 activated coir pith carbon.

    PubMed

    Namasivayam, C; Sangeetha, D

    2006-07-31

    The abundant lignocellulosic agricultural waste, coir pith is used to develop ZnCl(2) activated carbon and applied to the removal of toxic anions, heavy metals, organic compounds and dyes from water. Sorption of inorganic anions such as nitrate, thiocyanate, selenite, chromium(VI), vanadium(V), sulfate, molybdate, phosphate and heavy metals such as nickel(II) and mercury(II) has been studied. Removal of organics such as resorcinol, 4-nitrophenol, catechol, bisphenol A, 2-aminophenol, quinol, O-cresol, phenol and 2-chlorophenol has also been investigated. Uptake of acidic dyes such as acid brilliant blue, acid violet, basic dyes such as methylene blue, rhodamine B, direct dyes such as direct red 12B, congo red and reactive dyes such as procion red, procion orange were also examined to assess the possible use of the adsorbent for the treatment of contaminated ground water. Favorable conditions for maximum removal of all adsorbates at the adsorbate concentration of 20 mg/L were used. Results show that ZnCl(2) activated coir pith carbon is effective for the removal of toxic pollutants from water.

  13. Removal and recovery of cobalt from aqueous solutions by adsorption using low cost lignocellulosic biomass--coir pith.

    PubMed

    Parab, Harshala; Joshi, Shreeram; Sudersanan, M; Shenoy, Niyoti; Lali, Arvind; Sarma, Umashankar

    2010-01-01

    The applicability of low-cost lignocellulosic biosorbent-coir pith, for removal of cobalt (II) from aqueous solutions using batch adsorption studies has been explored herein. Adsorption characteristics of coir pith were investigated systematically by varying the experimental parameters such as, solution pH, initial metal ion concentration, contact time, adsorbent dose and temperature. The studies revealed that optimum adsorption of cobalt onto coir pith occurred in the pH range of 4.0 - 7.0. Sorption kinetics of cobalt was found to be quite rapid under ambient conditions and the process followed second-order kinetics. The experimental data have been analyzed using non-linearized forms of Langmuir, Freundlich and Redlich-Peterson adsorption isotherms for mathematical description of the process. Desorption studies showed that the quantitative recovery of Co (II) from the spent coir pith was achieved by using 0.5 N HCl. The suitability of this adsorbent for real situation has been observed, when complete removal of cobalt from nuclear power plant coolant water was obtained. The present studies successfully demonstrated the use of coir pith as an efficient adsorbent material for removal of cobalt from aqueous solutions.

  14. 21 CFR 177.1010 - Acrylic and modified acrylic plastics, semirigid and rigid.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Acrylic and modified acrylic plastics, semirigid... Acrylic and modified acrylic plastics, semirigid and rigid. Semirigid and rigid acrylic and modified acrylic plastics may be safely used as articles intended for use in contact with food, in accordance...

  15. 21 CFR 177.1010 - Acrylic and modified acrylic plastics, semirigid and rigid.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylic and modified acrylic plastics, semirigid... Acrylic and modified acrylic plastics, semirigid and rigid. Semirigid and rigid acrylic and modified acrylic plastics may be safely used as articles intended for use in contact with food, in accordance...

  16. 21 CFR 177.1010 - Acrylic and modified acrylic plastics, semirigid and rigid.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Acrylic and modified acrylic plastics, semirigid... Acrylic and modified acrylic plastics, semirigid and rigid. Semirigid and rigid acrylic and modified acrylic plastics may be safely used as articles intended for use in contact with food, in accordance...

  17. 21 CFR 177.1010 - Acrylic and modified acrylic plastics, semirigid and rigid.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Acrylic and modified acrylic plastics, semirigid... Components of Single and Repeated Use Food Contact Surfaces § 177.1010 Acrylic and modified acrylic plastics, semirigid and rigid. Semirigid and rigid acrylic and modified acrylic plastics may be safely used...

  18. 21 CFR 177.1010 - Acrylic and modified acrylic plastics, semirigid and rigid.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Acrylic and modified acrylic plastics, semirigid... Acrylic and modified acrylic plastics, semirigid and rigid. Semirigid and rigid acrylic and modified acrylic plastics may be safely used as articles intended for use in contact with food, in accordance...

  19. Surface modification of coir fibre involving oxidation of lignins followed by reaction with furfuryl alcohol: Characterization and stability

    NASA Astrophysics Data System (ADS)

    Saw, Sudhir Kumar; Sarkhel, Gautam; Choudhury, Arup

    2011-02-01

    In this study, the chemical treatment of the coir fibres was executed through oxidation with aqueous ClO2 followed by grafting with furfuryl alcohol (FA), leading to create a coating around the fibres more compatible with the polymeric matrices. The ClO2 was used to oxidize mainly phenolic syringyl and guaiacyl units of the lignin polymer to create quinones, which were characterized by UV-vis spectroscopy and Fourier transform infrared spectroscopy. In addition, the surface features of modified fibres were studied using scanning electron microscopy. The extent of FA-grafting was found higher (weight gain 17.7%) for oxidized fibre compared to those for non-oxidized fibre (weight gain 2.2%). The surface modification with FA-grafting reduced the hydrophilicity of the coir fibre, as confirm by the dynamic contact angle and water absorption measurements. The thermal and mechanical properties of untreated, oxidized and FA-grafted coir fibres were evaluated and compared.

  20. Surfactant modified coir pith, an agricultural solid waste as adsorbent for phosphate removal and fertilizer carrier to control phosphate release.

    PubMed

    Namasivayam, C; Kumar, M V Suresh

    2005-10-01

    The surface of coir pith, an agricultural solid waste was modified using a cationic surfactant, hexadecyltrimethylammonium bromide (HDTMA) and the modified coir pith was investigated to assess the capacity for the removal of phosphate from aqueous solution. Optimum pH for maximum phosphate adsorption was found to be 4.0. Langmuir and Freundlich isotherms were used to model the adsorption equilibrium data. Kinetic studies showed that the adsorption obeyed second order kinetics. Thermodynamic parameters were evaluated and the overall adsorption process was spontaneous and endothermic. Effect of coexisting anions has also been studied. The feasibility of using spent adsorbent as fertilizer carrier to control phosphate release was also investigated.

  1. Platelet adhesion, contact phase coagulation activation, and C5a generation of polyethylene glycol acid-grafted high flux cellulosic membrane with varieties of grafting amounts.

    PubMed

    Fushimi, F; Nakayama, M; Nishimura, K; Hiyoshi, T

    1998-10-01

    Grafting of polyethylene glycol chains onto cellulosic membrane can be expected to reduce the interaction between blood (plasma protein and cells) and the membrane surface. Alkylether carboxylic acid (PEG acid) grafted high flux cellulosic membranes for hemodialysis, in which the polyethylene glycol chain bears an alkyl group at one side and a carboxyl group at the other side, have been developed and evaluated. PEG acid-grafted high flux cellulosic membranes with various grafting amounts have been compared with respect to platelet adhesion, the contact phase of blood coagulation, and complement activation in vitro. A new method of quantitating platelet adhesion on hollow-fiber membrane surfaces has been developed, which is based on the determination of lactate dehydrogenase (LDH) activity after lysis of the adhered platelets. PEG acid-grafted high flux cellulosic membranes showed reduced platelet adhesion and complement activation effects in grafting amounts of 200 ppm or higher without detecting adverse effects up to grafting amounts of 850 ppm. The platelet adhesion of a PEG acid-grafted cellulosic membrane depends on both the flux and grafting amounts of the membrane. It is concluded that the grafting of PEG acid onto a cellulosic membrane improves its biocompatibility as evaluated in terms of platelet adhesion, complement activation, and thrombogenicity.

  2. Adsorptive removal of 2-chlorophenol by low-cost coir pith carbon.

    PubMed

    Namasivayam, C; Kavitha, D

    2003-03-17

    Adsorption of 2-chlorophenol (2-CP) by coir pith carbon was carried out by varying the parameters such as agitation time, 2-CP concentration, adsorbent dose, pH and temperature. Adsorption equilibrium reached at 40, 60, 80 and 100 min for 2-CP concentration of 10, 20, 30 and 40 mg/l, respectively. Adsorption followed second-order kinetics. The adsorption equilibrium data obeyed Freundlich isotherm. Acidic pH was favorable for the adsorption of 2-CP. Desorption studies showed that chemisorption plays a major role in the adsorption process.

  3. Participatory research using coir geotextiles in watershed management A case study in south India

    NASA Astrophysics Data System (ADS)

    Vishnudas, Subha; Savenije, Hubert H. G.; van der Zaag, Pieter; Anil, Kunnathu R.; Balan, Krishnan

    This paper deals with participatory research on the introduction and use of coir geotextiles for soil and water conservation in a small community pond in a watershed in south India. The results demonstrate that a participatory approach enables the community to visualize and evaluate the impact of innovative technologies. As a result, farmers readily adapt a technology when they have experienced the positive research outcome. This reduces the adoption time, and can bring significant increase in yield, or decrease in labour costs, helping to enhance productivity, sustainability and improvement of livelihood.

  4. Effect of fiber treatments on tensile and thermal properties of starch/ethylene vinyl alcohol copolymers/coir biocomposites

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The effects of different fiber treatments, namely washing with water, alkali treatment (mercerization) and bleaching, on mechanical and thermal properties of starch/EVA/coir biocomposites were evaluated by tensile tests and thermogravimetry (TG), respectively. Additionally, the fiber/matrix interfac...

  5. Engineering a lignocellulosic biosorbent--coir pith for removal of cesium from aqueous solutions: equilibrium and kinetic studies.

    PubMed

    Parab, Harshala; Sudersanan, M

    2010-02-01

    A novel method of engineering lignocellulosic biosorbent- coir pith (CP) by incorporation of nickel hexacyanoferrate (NiHCF), also referred to as Prussian blue analogue (PBA) inside its porous matrix is reported. Structural characterization confirmed the successful synthesis of NiHCF in the coir pith matrix. Sorption capacity of coir pith (CP) before and after loading of NiHCF was investigated for cesium (Cs) in batch equilibrium studies. Kinetic studies showed that the sorption process was rapid and saturation was attained within 30 min. The applicability of non linear Langmuir, Freundlich and Redlich Peterson isotherms was examined for the experimental data. The present studies revealed that there was nearly 100% increase in the sorption capacity of CP after its surface modification with NiHCF. Owing to its low cost, fast sorption kinetics and high uptake capacity, coir pith loaded with NiHCF (CP-NiHCF) seems to be one of the most promising biosorbents for recovery of cesium from liquid nuclear wastes.

  6. Removal of molybdate from water by adsorption onto ZnCl2 activated coir pith carbon.

    PubMed

    Namasivayam, C; Sangeetha, D

    2006-07-01

    Removal and recovery of molybdate from aqueous solution was investigated using ZnCl2 activated carbon developed from coir pith. Studies were conducted to delineate the effects of contact time, adsorbent dose, molybdate concentration, pH and temperature. Two theoretical adsorption isotherms, namely, Langmuir and Freundlich were used to describe the experimental results. The Langmuir adsorption capacity (Q0) was found to be 18.9 mg molybdate/g of the adsorbent. Adsorption followed second order kinetics. Studies were performed at different pH values to find out the pH at which maximum adsorption occurred. The pH effect and desorption studies showed that ion exchange and chemisorption mechanism were involved in the adsorption process. Thermodynamic parameters such as DeltaG0, DeltaH0 and DeltaS0 for the adsorption were evaluated. Effect of foreign ions on adsorption of molybdate has been examined. The results showed that ZnCl2 activated coir pith carbon was effective for the removal and recovery of molybdate from water.

  7. Removal of reactive dyes from wastewater by adsorption on coir pith activated carbon.

    PubMed

    Santhy, K; Selvapathy, P

    2006-07-01

    The removal efficiency of activated carbon prepared from coir pith towards three highly used reactive dyes in textile industry was investigated. Batch experiments showed that the adsorption of dyes increased with an increase in contact time and carbon dose. Maximum de-colorisation of all the dyes was observed at acidic pH. Adsorption of dyes was found to follow the Freundlich model. Kinetic studies indicated that the adsorption followed first order and the values of the Lagergren rate constants of the dyes were in the range of 1.77 x 10(-2)-2.69 x 10(-2)min(-1). The column experiments using granular form of the carbon (obtained by agglomeration with polyvinyl acetate) showed that adsorption efficiency increased with an increase in bed depth and decrease of flow rate. The bed depth service time (BDST) analysis carried out for the dyes indicated a linear relationship between bed depth and service time. The exhausted carbon could be completely regenerated and put to repeated use by elution with 1.0M NaOH. The coir pith activated carbon was not only effective in removal of colour but also significantly reduced COD levels of the textile wastewater.

  8. Poly(2-vinylnaphthalene-alt-maleic acid)-graft polystyrene as a photoactive polymer micelle and stabilizer for polystyrene latexes

    SciTech Connect

    Cao, T.; Yin, W.; Webber, S.E. )

    1994-12-05

    Polymerization of maleic anhydride and 2-vinylnaphthalene produces alternating polymers. Imidization of the polymer with amino-terminated polystyrene yields different loadings of an alternating polymer with polystyrene combs''. Upton rigorous hydrolysis one obtains poly(2-vinylnaphthalene-alt-maleic acid)-graft-polystyrene (P2VNMA-PS), which is a fluorescent polymer with unusual solution properties and with significant surface activity. P2VNMA-PS forms a small micelle structure in solution or can be used as a surfactant for an emulsion polymerization of polystyrene (no cosurfactant is required), producing monodisperse latex particles which are stable for pH > 3.9. Centrifugation shows that >90% of the P2VNMA-PS is associated with the latex particles. Fluorescence quenching studies of the naphthalene excimer with Tl[sup +] indicate that approximately 84% and 77% of the naphthalene groups remain exposed to the aqueous phase when this polymer is micellized or incorporated onto a latex particle, respectively. These data imply that the P2VNMA-PS polymer is permanently associated with the exterior of the latex particle, as one would expect given the amphiphilic nature of this polymer.

  9. Effect of stearic acid-grafted starch compatibilizer on properties of linear low density polyethylene/thermoplastic starch blown film.

    PubMed

    Khanoonkon, Nattaporn; Yoksan, Rangrong; Ogale, Amod A

    2016-02-10

    The present work aims to investigate the effect of stearic acid-grafted starch (ST-SA) on the rheological, thermal, optical, dynamic mechanical thermal, and tensile properties of linear low density polyethylene/thermoplastic starch (LLDPE/TPS) blends, as well as on their water vapor and oxygen barrier properties. Blends consisting of LLDPE and TPS in a weight ratio of 60:40 and ST-SA at different concentrations, i.e. 1, 3 and 5%, were prepared using a twin-screw extruder. The obtained resins were subsequently converted into films via blown film extrusion. Incorporation of ST-SA resulted in a decreased degree of shear thinning, reduced ambient temperature elasticity, and improved tensile strength, secant modulus, extensibility, and UV absorption, as well as diminished water vapor and oxygen permeabilities of the LLDPE/TPS blend. These effects are attributed to the enhanced interfacial adhesion between LLDPE and TPS phases through the compatibilizing effect induced by ST-SA, and the good dispersion of the TPS phase in the LLDPE matrix. The results confirmed that ST-SA could potentially be used as a compatibilizer for the LLDPE/TPS blend system.

  10. Folic acid-grafted bovine serum albumin decorated graphene oxide: An efficient drug carrier for targeted cancer therapy.

    PubMed

    Ma, Naxin; Liu, Jing; He, Wenxiu; Li, Zhonghao; Luan, Yuxia; Song, Yunmei; Garg, Sanjay

    2017-03-15

    Targeting drug carrier systems based on graphene oxide (GO) are of great interest, since it can selectively deliver anticancer drugs to tumor cells, and enhance therapeutic activities with minimized side effects. However, direct grafting target molecules on GO usually results in aggregation of physiological fluid, limiting its biomedical applications. Here, we propose a new strategy to construct targeting GO drug carrier using folic acid grafted bovine serum albumin (FA-BSA) as both the stabilizer and targeting agent. FA-BSA decorated graphene oxide-based nanocomposite (FA-BSA/GO) was fabricated by the physical adsorption of FA-BSA on GO, which was developed as a targeting drug delivery carrier. FA-BSA/GO as the drug carrier was associated with anticancer drug doxorubicin (DOX) through π-π and hydrogen-bond interactions, resulting in high drug loading (up to 437.43μgDOX/mgFA-BSA/GO). FA-BSA/GO/DOX systems demonstrated pH responsive and sustained drug release. The hemolysis ratio of FA-BSA/GO was less than 5%, demonstrating its safety as drug carrier for intravenous injection. Moreover, in vitro cell cytotoxicity and cellular uptake analysis suggested that the constructed FA-BSA/GO/DOX nanohybrids could significantly enhance the anticancer activity. The present work has confirmed the potential for fabrication of highly stable and dispersible GO-based targeting delivery systems for efficient cancer therapy.

  11. Finite-Element Analysis of Jute- and Coir-Fiber-Reinforced Hybrid Composite Multipanel Plates

    NASA Astrophysics Data System (ADS)

    Nirbhay, M.; Misra, R. K.; Dixit, A.

    2015-09-01

    Natural-fiber-reinforced polymer composite materials are rapidly gaining interest worldwide both in terms of research and industrial applications. The present work includes the characterization and modeling of jute- and coir-fiber-reinforced hybrid composite materials. The mechanical behavior of a two-panel plate and a sixpanel box structure is analyzed under various loading regimes by using the finite-element software ABAQUS®. Exhaustive parametric studies are also performed to obtain a clear insight into the relationships between various parameters and deflections of the panels and stress distributions in them. Deflections of both the structures are compared and found to be in good agreement with published results. To determine the mechanical behavior of natural-fiber-reinforced composite panels, a finite-element analysis is performed.

  12. Adsorption characteristics of cadmium(II) onto functionalized poly(hydroxyethylmethacrylate)-grafted coconut coir pith.

    PubMed

    Anirudhan, Thayyath Sreenivasan; Divya, Lekshmi; Rijith, Sreenivasan

    2010-07-01

    This study explored the feasibility of utilizing a novel adsorbent, poly(hydroxyethylmethacrylate)-grafted coconut coir pith with carboxyl functionality (PGCP-COOH) for the removal of cadmium(II) from water and wastewater. Maximum removal of 99.9% was observed for an initial concentration of 25 mg/L at pH 6.0 and adsorbent dose of 2.0 g/L. The first-order reversible kinetic model and Langmuir isotherm model were resulted in high correlation coefficients and described well the adsorption of Cd(II) onto PGCP-COOH. The complete removal of 22.4 mg/L Cd(II) from fertilizer industry wastewater was achieved by 2.0 g/L PGCP-COOH. The reusability of the PGCP-COOH for several cycles was demonstrated using 0.1 M HCl solution.

  13. Uptake of dyes by a promising locally available agricultural solid waste: coir pith.

    PubMed

    Namasivayam, C; Radhika, R; Suba, S

    2001-01-01

    The adsorption of rhodamine-B and acid violet by coir pith carbon was carried out by varying the parameters such as agitation time, dye concentration, adsorbent dose and pH. The adsorption followed both Langmuir and Freundlich isotherms. The adsorption capacity was found to be 2.56 mg and 8.06 mg dye per g of the adsorbent for rhodamine-B and acid violet, respectively. Adsorption of dyes followed first order rate kinetics. Acidic pH was favorable for the adsorption of acid violet and alkaline pH was favorable to rhodamine-B. Desorption studies showed that alkaline pH was favorable for the desorption of acid violet and acidic pH was favorable for the desorption of rhodamine-B.

  14. A reinvestigation of EXAFS and EPR spectroscopic measurements of chromium(VI) reduction by coir pith.

    PubMed

    Suksabye, Parinda; Worasith, Niramon; Thiravetyan, Paitip; Nakajima, Akira; Goodman, Bernard A

    2010-08-15

    New measurements using extended X-ray absorption fine structure (EXAFS) and electron paramagnetic resonance (EPR) techniques are consistent with Cr in the Cr(III) oxidation state as the main product from the adsorption of Cr(VI) on coir pith. These confirm the previous X-ray measurements, but differ from the results of previous EPR studies, which indicated that Cr(V) was the main form of Cr. The reason for this discrepancy is the presence of a broad signal from Cr(III) in an unsymmetrical environment that was missed previously; the Cr(V) component is in fact only a minor reaction product. As a result of this problem with spectral acquisition and interpretation, some simple recommendations are presented for conducting EPR investigations on natural systems.

  15. Fabrication of borassus fruit lignocellulose fiber/PP composites and comparison with jute, sisal and coir fibers.

    PubMed

    Sudhakara, P; Jagadeesh, Dani; Wang, YiQi; Prasad, C Venkata; Devi, A P Kamala; Balakrishnan, G; Kim, B S; Song, J I

    2013-10-15

    Novel composites based on borassus fruit fine fiber (BFF) and polypropylene (PP) were fabricated with variable fiber composition (5, 10, 15 and 20 wt%) by injection molding. Maleated PP (MAPP) was also used as compatibilizer at 5 wt% for effective fiber-matrix adhesion. FTIR analysis confirms the evidence of a chemical bonding between the fiber and polymeric matrix through esterification in presence of MAPP. The tensile and flexural properties were found to increase with 15 and 10 wt% fiber loadings respectively, and decreased thereafter. Coir, jute and sisal fiber composites were also fabricated with 15 wt% fiber loading under the same conditions as used for BFF/PP composites. It was found that the mechanical properties of BFF (15 wt%)/PP composites were equivalent to jute/PP, sisal/PP and superior to coir/PP composites. Jute/PP and sisal/PP composites showed higher water absorption than BFF/PP and coir/PP composites. These results have demonstrated that the BFF/PP composites can also be an alternative material for composites applications.

  16. 40 CFR 721.2805 - Acrylate ester.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Acrylate ester. 721.2805 Section 721... Acrylate ester. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as an acrylate ester (PMN P-96-824) is subject to reporting under...

  17. 40 CFR 721.2805 - Acrylate ester.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Acrylate ester. 721.2805 Section 721... Acrylate ester. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as an acrylate ester (PMN P-96-824) is subject to reporting under...

  18. 40 CFR 721.2805 - Acrylate ester.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Acrylate ester. 721.2805 Section 721... Acrylate ester. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as an acrylate ester (PMN P-96-824) is subject to reporting under...

  19. 40 CFR 721.2805 - Acrylate ester.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Acrylate ester. 721.2805 Section 721... Acrylate ester. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as an acrylate ester (PMN P-96-824) is subject to reporting under...

  20. 63 FR 41279 - Acrylic Sheet From Japan

    Federal Register 2010, 2011, 2012, 2013, 2014

    1998-08-03

    ... COMMISSION Acrylic Sheet From Japan AGENCY: United States International Trade Commission. ACTION: Institution of a five-year review concerning the antidumping duty order on acrylic sheet from Japan. SUMMARY: The... order on acrylic sheet from Japan would be likely to lead to continuation or recurrence of...

  1. 78 FR 55644 - Styrene, Copolymers with Acrylic Acid and/or Methacrylic Acid; Tolerance Exemption

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-09-11

    ... methacrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, and/or hydroxyethyl acrylate; and its sodium... methacrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, and/or hydroxyethyl acrylate; and its sodium... methacrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, and/or hydroxyethyl acrylate, and its...

  2. Mixing It Up with Acrylics.

    ERIC Educational Resources Information Center

    Laird, Shirley

    1999-01-01

    Presents an art activity for fifth-grade students in which they learn about basic shapes and what happens when shapes overlap, draw seven overlapping geometric shapes, review the use of acrylic paint and mixing colors, and finally paint with primary colors. (CMK)

  3. Drug release behavior of poly (lactic-glycolic acid) grafting from sodium alginate (ALG-g-PLGA) prepared by direct polycondensation.

    PubMed

    Shi, Gang; Ding, Yuanyuan; Zhang, Xin; Wu, Luyan; He, Fei; Ni, Caihua

    2015-01-01

    Hydrophobically modified sodium alginate, poly (lactic-glycolic acid) grafting from sodium alginate (ALG-g-PLGA), was successfully synthesized through direct one-step polymerization of sodium alginate, glycolic acid, and lactic acid. ALG-g-PLGA self-assembled to colloidal nanoparticles and subsequently hydrogel microspheres were obtained by crosslinking ALG-g-PLGA nanoparticles in the solution of calcium chloride. The modified hydrogel microspheres could be used as the drug delivery vehicles for a hydrophobic ibuprofen. Compared with sodium alginate, ALG-g-PLGA demonstrated an improved drug loading rate, encapsulation efficiency, and prolonged release speed. The products, as novel and highly promising biomaterials, have potential applications.

  4. Study of physical and sound absorbing property of epoxy blended coir dust biocomposite

    NASA Astrophysics Data System (ADS)

    Nath, G.; Mishra, S. P.

    2016-09-01

    Reinforcement biocomposite has gained more attention recently due to its low cost, abundantly availability, low density, specific properties, easy method of separation, enhanced energy recovery, CO2 neutrality, biodegradability and recyclable in nature. As a waste product of coconut fruit, the coconut coir dust (CCD) obtained from the coconut husk. The biocomposite material prepared from the CCD modified with the proper blended solution with the help of ultrasonic technique. The study of adiabatic compressibility of acetone / water (70/30) worth its blending property for bleaching of CCD. The biocomposite material of CCD was prepared with epoxy resin. The different physical properties such as sound absorption coefficient, thermal conductivity and electrical conductivity were measured. The morphological study of biocomposite and measurement of sound absorption coefficient shows good evidence of sound absorbing characteristics of biocomposite of CCD. The sound absorption property of composite material shows a significant result where as the thermal conductivity and electrical conductivity executes a weak result. Thus biocomposite of CCD can acts as a good sound absorber and band conductor of heat and electric current.

  5. Removal of phenol and chlorophenols from water by coir pith carbon: equilibrium and rate studies.

    PubMed

    Namasivayam, C; Kavitha, D

    2004-07-01

    Batch mode studies were conducted to study the removal of phenol, 2,4,6-Trichlorophenol (TCP) and Pentachlorophenol (PCP) from aqueous solution on coir pith carbon by adsorption process under varying experimental conditions such as agitation time, adsorbent dose, pH and temperature. Kinetics of adsorption obeyed second order rate equation and the rate constant was found to be in the range 0.0098-0.0672, 0.0949-0.8801 and 0.172-0.305 g/mg/min for phenol, TCP and PCP respectively. Equilibrium adsorption data follow Langmuir isotherm for phenol and PCP and the adsorption capacities were found to be 48.3 mg and 3.7 mg/g, respectively. For TCP, adsorption followed Freundlich isotherm only. Acidic pH was favorable for the adsorption of all the chlorophenols. Studies on pH effect and desorption show that chemisorption seems to play a major rule in the adsorption process. The positive values of H0 24.99, 18.69, and 8.907 kJ/mol for phenol, TCP and PCP respectively, confirm the endothermic nature of adsorption.

  6. Biodegradation of toluene vapor in coir based upflow packed bed reactor by Trichoderma asperellum isolate.

    PubMed

    Gopinath, M; Mohanapriya, C; Sivakumar, K; Baskar, G; Muthukumaran, C; Dhanasekar, R

    2016-03-01

    In the present study, a new biofiltration system involving a selective microbial strain isolated from aerated municipal sewage water attached with coir as packing material was developed for toluene degradation. The selected fungal isolate was identified as Trichoderma asperellum by 16S ribosomal RNA (16S rRNA) sequencing method, and pylogenetic tree was constructed using BLASTn search. Effect of various factors on growth and toluene degradation by newly isolated T. asperellum was studied in batch studies, and the optimum conditions were found to be pH 7.0, temperature 30 °C, and initial toluene concentration 1.5 (v/v)%. Continuous removal of gaseous toluene was monitored in upflow packed bed reactor (UFPBR) using T. asperellum. Effect of various parameters like column height, flow rate, and the inlet toluene concentration were studied to evaluate the performance of the biofilter. The maximum elimination capacity (257 g m(-3) h(-1)) was obtained with the packing height of 100 cm with the empty bed residence time of 5 min. Under these optimum conditions, the T. asperellum showed better toluene removal efficiency. Kinetic models have been developed for toluene degradation by T. asperellum using macrokinetic approach of the plug flow model incorporated with Monod model.

  7. Carboxylic acid-grafted mesoporous material and its high catalytic activity in one-pot three-component coupling reaction

    NASA Astrophysics Data System (ADS)

    Gomes, Ruth; Dutta, Saikat; Bhaumik, Asim

    2014-11-01

    A new carboxylic acid functionalized mesoporous organic polymer has been synthesized via in situ radical polymerization of divinylbenzene and acrylic acid using a mesoporous silica as a seed during the polymerization process under solvothermal conditions. The mesoporous material MPDVAA-1 has been thoroughly characterized employing powder XRD, solid state 13C cross polarization magic angle spinning-nuclear magnetic resonance, FT-IR spectroscopy, N2 sorption, HR-TEM, and NH3 temperature programmed desorption-thermal conductivity detector (TPD-TCD) analysis to understand its porosity, chemical environment, bonding, and surface properties. The mesoporous polymer was used as a catalyst for a three comp onent Biginelli condensation between various aldehydes, β-keto esters, and urea/thioureas to give 3,4-dihydropyrimidine-2(1H)-ones. The reactions were carried out under conventional heating as well as solvent-free microwave irradiation of solid components, and in both the cases, the mesoporous polymer MPDVAA-1 proved to be a powerful, robust, and reusable catalyst with high catalytic efficiency.

  8. Carboxylic acid-grafted mesoporous material and its high catalytic activity in one-pot three-component coupling reaction

    SciTech Connect

    Gomes, Ruth; Bhaumik, Asim; Dutta, Saikat

    2014-11-01

    A new carboxylic acid functionalized mesoporous organic polymer has been synthesized via in situ radical polymerization of divinylbenzene and acrylic acid using a mesoporous silica as a seed during the polymerization process under solvothermal conditions. The mesoporous material MPDVAA-1 has been thoroughly characterized employing powder XRD, solid state {sup 13}C cross polarization magic angle spinning-nuclear magnetic resonance, FT-IR spectroscopy, N{sub 2} sorption, HR-TEM, and NH{sub 3} temperature programmed desorption-thermal conductivity detector (TPD-TCD) analysis to understand its porosity, chemical environment, bonding, and surface properties. The mesoporous polymer was used as a catalyst for a three comp onent Biginelli condensation between various aldehydes, β-keto esters, and urea/thioureas to give 3,4-dihydropyrimidine-2(1H)-ones. The reactions were carried out under conventional heating as well as solvent-free microwave irradiation of solid components, and in both the cases, the mesoporous polymer MPDVAA-1 proved to be a powerful, robust, and reusable catalyst with high catalytic efficiency.

  9. The effectiveness of jute and coir blankets for erosion control in different field and laboratory conditions

    NASA Astrophysics Data System (ADS)

    Kalibová, Jana; Jačka, Lukáš; Petrů, Jan

    2016-03-01

    Vegetation cover is found to be an ideal solution to most problems of erosion on steep slopes. Biodegradable geotextiles (GTXs) have been proved to provide sufficient protection against soil loss in the period before vegetation reaches maturity, so favouring soil formation processes. In this study, 500 g m-2 jute (J500), 400 g m-2 (C400), and 700 g m-2 coir (C700) GTXs were first installed on a 9° slope under "no-infiltration" laboratory conditions, then on a 27° slope under natural field conditions. The impact of GTXs on run-off and soil loss was investigated to compare the performance of GTXs under different conditions. Laboratory run-off ratio (percentage portion of control plot) equalled 78, 83, and 91 %, while peak discharge ratio equalled 83, 91, and 97 % for J500, C700, and C400 respectively. In the field, a run-off ratio of 31, 62, and 79 %, and peak discharge ratio of 37, 74, and 87 % were recorded for C700, J500, and C400 respectively. All tested GTXs significantly decreased soil erosion. The greatest soil loss reduction in the field was observed for J500 (by 99.4 %), followed by C700 (by 97.9 %) and C400 (by 93.8 %). Irrespective of slope gradient or experimental condition, C400 performed with lower run-off and peak discharge reduction than J500 and C700. The performance ranking of J500 and C700 in the laboratory differed from the field, which may be explained by different slope gradients, and also by the role of soil, which was not included in the laboratory experiment.

  10. Experimental investigation on an entrained flow type biomass gasification system using coconut coir dust as powdery biomass feedstock.

    PubMed

    Senapati, P K; Behera, S

    2012-08-01

    Based on an entrained flow concept, a prototype atmospheric gasification system has been designed and developed in the laboratory for gasification of powdery biomass feedstock such as rice husks, coconut coir dust, saw dust etc. The reactor was developed by adopting L/D (height to diameter) ratio of 10, residence time of about 2s and a turn down ratio (TDR) of 1.5. The experimental investigation was carried out using coconut coir dust as biomass feedstock with a mean operating feed rate of 40 kg/h The effects of equivalence ratio in the range of 0.21-0.3, steam feed at a fixed flow rate of 12 kg/h, preheat on reactor temperature, product gas yield and tar content were investigated. The gasifier could able to attain high temperatures in the range of 976-1100 °C with gas lower heating value (LHV) and peak cold gas efficiency (CGE) of 7.86 MJ/Nm3 and 87.6% respectively.

  11. Removal of nutrients in denitrification system using coconut coir fibre for the biological treatment of aquaculture wastewater.

    PubMed

    Manoj, Valsa Remony; Vasudevan, Namasivayam

    2012-03-01

    Ideal bacterial support medium for fixed film denitrification processes/bioreactors must be inexpensive, durable and possess large surface area with sufficient porosity. The present study has been focussed on removing nitrate nitrogen at two different nitrate nitrogen loading rates (60 (NLR I) and 120 (NLR II) mg l(-1)) from simulated aquaculture wastewater. Coconut coir fibre and a commercially available synthetic reticulated plastic media (Fujino Spirals) were used as packing medium in two independent upflow anaerobic packed bed column reactors. Removal of nitrate nitrogen was studied in correlation with other nutrients (COD, TKN, dissolved orthophosphate). Maximum removal of 97% at NLR-I and 99% at NLR - II of nitrate nitrogen was observed in with either media. Greater consistency in the case of COD removal of upto 81% was observed at NLR II where coconut coir was used as support medium compared to 72% COD removal by Fujino Spirals. The results observed indicate that the organic support medium is just as efficient in nitrate nitrogen removal as conventionally used synthetic support medium. The study is important as it specifically focuses on denitrification of aquaculture wastewater using cheaper organic support medium in anoxic bioreactors for the removal of nitrate nitrogen; which is seldom addressed as a significant problem.

  12. Radiopurity measurement of acrylic for DEAP-3600

    SciTech Connect

    Nantais, C. M.; Boulay, M. G.; Cleveland, B. T.

    2013-08-08

    The spherical acrylic vessel that contains the liquid argon target is the most critical detector component in the DEAP-3600 dark matter experiment. Alpha decays near the inner surface of the acrylic vessel are one of the main sources of background in the detector. A fraction of the alpha energy, or the recoiling nucleus from the alpha decay, could misreconstruct in the fiducial volume and result in a false candidate dark matter event. Acrylic has low levels of inherent contamination from {sup 238}U and {sup 232}Th. Another background of particular concern is diffusion of {sup 222}Rn during manufacturing, leading to {sup 210}Pb contamination. The maximum acceptable concentrations in the DEAP-3600 acrylic vessel are ppt levels of {sup 238}U and {sup 232}Th equivalent, and 10{sup −8} ppt {sup 210}Pb. The impurities in the bulk acrylic will be measured by vaporizing a large quantity of acrylic and counting the concentrated residue with ultra-low background HPGe detectors and a low background alpha spectrometer. An overview of the acrylic assay technique is presented.

  13. 21 CFR 177.1060 - n-Alkylglutarimide/acrylic copolymers.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false n-Alkylglutarimide/acrylic copolymers. 177.1060... Use Food Contact Surfaces § 177.1060 n-Alkylglutarimide/acrylic copolymers. n-Alkylglutarimide/acrylic...) Identity. For the purpose of this section, n-alkylglutarimide/acrylic copolymers are copolymers obtained...

  14. 21 CFR 175.210 - Acrylate ester copolymer coating.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Acrylate ester copolymer coating. 175.210 Section... Coatings § 175.210 Acrylate ester copolymer coating. Acrylate ester copolymer coating may safely be used as... prepared food, subject to the provisions of this section: (a) The acrylate ester copolymer is a...

  15. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  16. Monolithic F-16 Uniform Thickness Stretched Acrylic Canopy Transparency Program

    DTIC Science & Technology

    1984-01-01

    Thermoforming Finite Strain Analysis Finite Element Modeling Mooney Formulation Tensile Testing Acrylic Material Properties F-16 Transparency Thinning Uniform...OF ACRYLIC TENSILE SPECIMEN ...... 8 MARC ANALYSIS OF ACRYLIC HEMISPHERE ............ 12 IV ACRYLIC MATERIAL PROPERTIES AT THERMOFORMING TEMPERATURES...properties (necessary for finite element stress analysis work) were generated at temperatures in the range of thermoforming . A finite element code

  17. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  18. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be...) Acrylamide-acrylic acid resins are produced by the polymerization of acrylamide with partial hydrolysis or...

  19. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  20. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  1. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  2. 21 CFR 177.1310 - Ethylene-acrylic acid copolymers.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ethylene-acrylic acid copolymers. 177.1310 Section... Use Food Contact Surfaces § 177.1310 Ethylene-acrylic acid copolymers. The ethylene-acrylic acid... for use in contact with food subject to the provisions of this section. (a) The ethylene-acrylic...

  3. Poly(meth)acrylate-based coatings.

    PubMed

    Nollenberger, Kathrin; Albers, Jessica

    2013-12-05

    Poly(meth)acrylate coatings for pharmaceutical applications were introduced in 1955 with the launch of EUDRAGIT(®) L and EUDRAGIT(®) S, two types of anionic polymers. Since then, by introducing various monomers into their polymer chains and thus altering their properties, diverse forms with specific characteristics have become available. Today, poly(meth)acrylates function in different parts of the gastrointestinal tract and/or release the drug in a time-controlled manner. This article reviews the properties of various poly(meth)acrylates and discusses formulation issues as well as application possibilities.

  4. New radiopaque acrylic bone cement. II. Acrylic bone cement with bromine-containing monomer.

    PubMed

    Rusu, M C; Ichim, I C; Popa, M; Rusu, M

    2008-07-01

    Bromine-containing methacrylate, 2-(2-bromopropionyloxy) ethyl methacrylate (BPEM), had been used in the formulation of acrylic radiopaque cements. The effect of this monomer incorporated into the liquid phase of acrylic bone cement, on the curing parameters, thermal properties, water absorption, density, compression tests and radiopacity was studied. A decrease of maximum temperature and an increase of the setting time were observed with the addition of the bromine-containing monomer in the radiolucent cement composition. Adding BPEM in radiolucent acrylic bone cements composition results in the decrease of glass transition temperature and increase of its thermal stability. Acrylic bone cements modified with bromine-containing comonomer are characterized by polymerization shrinkage lower than the radiolucent cement. Addition of bromine-containing comonomer in radiolucent acrylic bone cement composition determines the increase of compressive strength. Acrylic bone cements modified with bromine-containing comonomer proved to be radiopaque.

  5. Equilibrium and kinetic studies of adsorption of phosphate onto ZnCl2 activated coir pith carbon.

    PubMed

    Namasivayam, C; Sangeetha, D

    2004-12-15

    Phosphate removal from aqueous solution was investigated using ZnCl(2)-activated carbon developed from coir pith, an agricultural solid waste. Studies were conducted to delineate the effect of contact time, adsorbent dose, phosphate concentration, pH, and temperature. The adsorption equilibrium data followed both Langmuir and Freundlich isotherms. Langmuir adsorption capacity was found to be 5.1 mg/g. Adsorption followed second-order kinetics. The removal was maximum in the pH range 3-10. pH effect and desorption studies showed that adsorption occurred by both ion exchange and chemisorption mechanisms. Adsorption was found to be spontaneous and endothermic. Effect of foreign ions on adsorption shows that perchlorate, sulfate, and selenite decreased the percent removal of phosphate.

  6. EVALUATION OF AN ACRYLATE TERPOLYMER, POLYURETHANE COMPOSITE.

    DTIC Science & Technology

    Composite films consisting of a flexible acrylate terpolymer substrate and an outer layer of poly (ester-urethane) elastomer were prepared and evaluated for use in cosmetic glove applications. (Author)

  7. Chemical Stress Cracking of Acrylic Fibers.

    DTIC Science & Technology

    1982-05-01

    nitrile groups (similar to the "prefatory reaction" in pyrolysis of acrylic fibers), followed immediately by N- chlorination and7 chain scission...cyclization of nitrile groups (similar to the "prefatory reaction" in pyrolysis of acrylic fibers), followed immediately by N- chlorination and chain scission...present experiments were conducted at the boil, slightly greater than 100 C. The decomposition products-- chlorine , chlorate, plus oxygen originating

  8. Changes in microbial properties and nutrient dynamics in bagasse and coir during vermicomposting: quantification of fungal biomass through ergosterol estimation in vermicompost.

    PubMed

    Pramanik, P

    2010-05-01

    In this experiment, different microorganisms viz., Trichoderma viridae, Aspergillus niger and Bacillus megaterium were inoculated in bagasse and coir with the objective to study their effect on nutrient dynamics and microbial properties, specially effect on fungal status in these waste materials. Fungal biomass (FBC) was calculated from the ergosterol content in the vermicompost samples. Inoculation of B. megaterium registered comparatively higher TP content in the final stabilized product. Vermicomposting increased microbial biomass carbon (MBC) and nitrogen (MBN) content in bagasse and coir. Microbial biomass carbon to nitrogen ratio (MBC/ MBN) was comparatively narrower in fungi inoculated vermicomposts and FBC/MBC ratio was increased up to 11.69 from 9.51 of control during vermicomposting.

  9. Effect of kojic acid-grafted-chitosan oligosaccharides as a novel antibacterial agent on cell membrane of gram-positive and gram-negative bacteria.

    PubMed

    Liu, Xiaoli; Xia, Wenshui; Jiang, Qixing; Xu, Yanshun; Yu, Peipei

    2015-09-01

    Our work here, for the first time, reported the antibacterial activity of kojic acid-grafted-chitosan oligosaccharides (COS/KA) against three gram-positive and three gram-negative bacteria. Integrity of cell membrane, outer membrane (OM) and inner membrane (IM) permeabilization assay, alkaline phosphatase (ALP) and glucose-6-phosphate dehydrogenase (G6PDH) assay, and SDS-PAGE assay techniques were used to investigate the interactions between COS/KA and bacterial membranes. The antibacterial activity of COS/KA was higher than those of unmodified COS. The electric conductivity of bacteria suspensions increased, followed by increasing of the units of average release for ALP and G6PDH. COS/KA can also rapidly increase the 1-N-phenylanphthylamine (NPN) uptake and the release of β-galactosidase via increasing the permeability of OM and IM in Escherichia coli. SDS-PAGE indicated the content of cellular soluble proteins decreased significantly in COS/KA-treated bacteria. Hence, COS/KA has potential in food industry and biomedical sciences.

  10. Effective removal of mercury(II) ions from chlor-alkali industrial wastewater using 2-mercaptobenzamide modified itaconic acid-grafted-magnetite nanocellulose composite.

    PubMed

    Anirudhan, T S; Shainy, F

    2015-10-15

    A novel adsorbent, 2-mercaptobenzamide modified itaconic acid-grafted-magnetite nanocellulose composite [P(MB-IA)-g-MNCC] was synthesized for adsorbing mercury(II) [Hg(II)] ions selectively from aqueous solutions. Fourier transforms infrared spectroscopy, X-ray diffraction, scanning electron microscopy and thermogravimetric studies were performed to characterize the adsorbent. The optimum pH for Hg(II) adsorption was found to be 8.0, and the adsorption attained equilibrium within 60 min. The kinetic data were found to follow pseudo-second-order which assumes the ion exchange followed by complexation mechanism. The temperature dependence indicates an exothermic process. The well agreement of equilibrium data with Freundlich adsorption model confirms the multilayer coverage of Hg(II) onto P(MB-IA)-g-MNCC. The maximum adsorption capacity was found to be 240.0 mg/g. Complete removal of Hg(II) from aqueous solution was possible with an adsorbent dosage of 2.0 g/L. Spent adsorbent was effectively degenerated with 0.1M HCl. The present investigation shows that P(MB-IA)g-MNCC is a promising adsorbent for the removal and recovery of Hg(II) ions from aqueous solutions.

  11. Self-assembled platinum nanoparticles on sulfonic acid-grafted graphene as effective electrocatalysts for methanol oxidation in direct methanol fuel cells

    PubMed Central

    Lu, Jinlin; Li, Yanhong; Li, Shengli; Jiang, San Ping

    2016-01-01

    In this article, sulfonic acid-grafted reduced graphene oxide (S-rGO) were synthesized using a one-pot method under mild conditions, and used as Pt catalyst supports to prepare Pt/S-rGO electrocatalysts through a self-assembly route. The structure, morphologies and physicochemical properties of S-rGO were examined in detail by techniques such as atomic force microscope (AFM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The S-rGO nanosheets show excellent solubility and stability in water and the average particle size of Pt nanoparticles supported on S-rGO is ~3.8 nm with symmetrical and uniform distribution. The electrocatalytic properties of Pt/S-rGO were investigated for methanol oxidation reaction (MOR) in direct methanol fuel cells (DMFCs). In comparison to Pt supported on high surface area Vulcan XC-72 carbon (Pt/VC) and Pt/rGO, the Pt/S-rGO electrocatalyst exhibits a much higher electrocatalytic activity, faster reaction kinetics and a better stability. The results indicate that Pt/S-rGO is a promising and effective electrocatalyst for MOR of DMFCs. PMID:26876468

  12. Self-assembled platinum nanoparticles on sulfonic acid-grafted graphene as effective electrocatalysts for methanol oxidation in direct methanol fuel cells

    NASA Astrophysics Data System (ADS)

    Lu, Jinlin; Li, Yanhong; Li, Shengli; Jiang, San Ping

    2016-02-01

    In this article, sulfonic acid-grafted reduced graphene oxide (S-rGO) were synthesized using a one-pot method under mild conditions, and used as Pt catalyst supports to prepare Pt/S-rGO electrocatalysts through a self-assembly route. The structure, morphologies and physicochemical properties of S-rGO were examined in detail by techniques such as atomic force microscope (AFM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The S-rGO nanosheets show excellent solubility and stability in water and the average particle size of Pt nanoparticles supported on S-rGO is ~3.8 nm with symmetrical and uniform distribution. The electrocatalytic properties of Pt/S-rGO were investigated for methanol oxidation reaction (MOR) in direct methanol fuel cells (DMFCs). In comparison to Pt supported on high surface area Vulcan XC-72 carbon (Pt/VC) and Pt/rGO, the Pt/S-rGO electrocatalyst exhibits a much higher electrocatalytic activity, faster reaction kinetics and a better stability. The results indicate that Pt/S-rGO is a promising and effective electrocatalyst for MOR of DMFCs.

  13. Synthesis and characterization of polyacrylic acid- grafted-carboxylic graphene/titanium nanotube composite for the effective removal of enrofloxacin from aqueous solutions: Adsorption and photocatalytic degradation studies.

    PubMed

    Anirudhan, Thayyath S; Shainy, F; Christa, J

    2017-02-15

    Polyacrylic acid-grafted-carboxylic graphene/titanium nanotube (PAA-g-CGR/TNT) composite was synthesized. It was effectively used as adsorbent as well as photocatalyst. The composite was characterized by FTIR, XRD, SEM, TEM, Surface Area Analyzer, XPS and DRS. The photocatalytic activity of PAA-g-CGR/TNT composite was evaluated on the basis of the degradation of pollutants by using sunlight. The band gap of the prepared photocatalyst was found to be 2.6eV. The removal of the antibiotic enrofloxacin (ENR) was achieved by two step mechanism based on adsorption and photodegradation. The maximum adsorption was observed at pH 5.0. The best fitted kinetic model was found to be pseudo-second-order. The maximum adsorption was observed at 30°C. The maximum adsorption capacity was found to be 13.40mg/g. The kinetics of photodegradation of ENR onto PAA-g-CGR/TNT composite follow first-order kinetics and optimum pH was found to be 5.0. The regeneration and reuse of the adsorbent-cum-photocatalyst were also examined upto five cycles.

  14. In vitro characterization of pH-sensitive azithromycin-loaded methoxy poly (ethylene glycol)-block-poly (aspartic acid-graft-imidazole) micelles.

    PubMed

    Teng, Fangfang; Deng, Peizong; Song, Zhimei; Zhou, Feilong; Feng, Runliang; Liu, Na

    2017-02-09

    In order to improve azithromycin's antibacterial activity in acidic medium, monomethoxy poly (ethylene glycol)-block-poly (aspartic acid-graft-imidazole) copolymer was synthesized through allylation, free radical addition, ring-opening polymerization and amidation reactions with methoxy poly (ethylene glycol) as raw material. Drug loading capacity and encapsulation efficiency of azithromycin-loaded micelles prepared via thin film hydration method were 11.58±0.86% and 96.06±1.93%, respectively. The drug-loaded micelles showed pH-dependent property in the respects of particle size, zeta potential at the range of pH 5.5-7.8. It could control drug in vitro release and demonstrate higher release rate at pH 6.0 than that at pH 7.4. In vitro antibacterial experiment indicated that the activity of azithromycin-loaded micelles against S. aureus was superior to free azithromycin in medium at both pH 6.0 and pH 7.4. Using fluorescein as substitute with pH-dependent fluorescence decrease property, laser confocal fluorescence microscopy analysis confirmed that cellular uptake of micelles was improved due to protonation of copolymer's imidazole groups at pH 6.0. The enhanced cellular uptake and release of drug caused its activity enhancement in acidic medium when compared with free drug. The micellar drug delivery system should be potential application in the field of bacterial infection treatment.

  15. Synthesis and characterization of carboxyl terminated poly(methacrylic acid) grafted chitosan/bentonite composite and its application for the recovery of uranium(VI) from aqueous media.

    PubMed

    Anirudhan, T S; Rijith, S

    2012-04-01

    A novel adsorbent poly(methacrylic acid)-grafted chitosan/bentonite (CTS-g-PMAA/Bent) composite was prepared through graft copolymerization reaction of methacrylic acid and chitosan in the presence of bentonite (Bent) and N,N'- methylenebisacrylamide as a crosslinker. The composite was well characterized using FTIR, XRD, XPS, SEM-EDS, surface area and zeta potential analyzers. The adsorption behavior of the composite toward uranium(VI) from aqueous media was studied under varying operating conditions of pH, concentration of U(VI), contact time, adsorbent dose and temperature. The optimum pH range for U(VI) adsorption was 5.5 at 30 °C. Concentration and temperature dependent rate constants were evaluated using pseudo-second-order kinetic model. The equilibrium data were correlated with the Langmuir isotherm model with an endothermic behavior. The equilibrium U(VI) sorption capacity was estimated to be 117.2 mg g(-1) at 30 °C. For the quantitative recovery of 100 mg L(-1) U(VI) from 1.0 L simulated nuclear industry wastewater, a minimum adsorbent dosage of 2.0 g CTS-g-PMAA/Bent was required. The calculated energy of activation (E(a) = 47.83 kJ/mol) was positively correlated with chemical adsorption process. The values of enthalpy, entropy and free energy of activation were calculated to explain the nature of adsorption process. Adsorption-desorption experiments over four cycles illustrate the feasibility of the repeated uses of this composite for the extraction of U(VI) from aqueous solutions.

  16. Antibacterial and synergic effects of gallic acid-grafted-chitosan with β-lactams against methicillin-resistant Staphylococcus aureus (MRSA).

    PubMed

    Lee, Dae-Sung; Eom, Sung-Hwan; Kim, Young-Mog; Kim, Hye Seon; Yim, Mi-Jin; Lee, Sang-Hoon; Kim, Do-Hyung; Je, Jae-Young

    2014-10-01

    Methicillin-resistant Staphylococcus aureus (MRSA) is spreading worldwide, emphasizing the need to search for new antibiotics. The anti-MRSA activities of gallic acid-grafted-chitosans (GA-g-chitosans) were investigated against 2 MRSA standards and 10 MRSA clinical isolates by determining the minimum inhibitory concentrations (MICs). GA-g-chitosan (I), which has the highest gallic acid content, exhibited the strongest anti-MRSA activities, with MICs of 32-64 μg/mL. A time-kill investigation revealed that GA-g-chitosan (I) exhibited a bactericidal effect at twice the MIC, also demonstrating good thermal and pH stability. Investigation of cell envelope integrity showed the release of intracellular components with an increasing absorbance value at 260 nm, indicating cell envelope damage caused by the GA-g-chitosan (I), which was further confirmed by transmission electron microscopy. When GA-g-chitosans were combined with β-lactams, including ampicillin and penicillin, synergistic effects were observed on the 2 standard MRSA strains and on the 10 clinical isolates, with fractional inhibitory indices ranging from 0.125 to 0.625. In the time-kill dynamic confirmation test, synergistic bactericidal effects were observed for the combinations of GA-g-chitosans with β-lactams, and over 4.0 log CFU/mL reductions were observed after 24 h when combination treatment was used. These results may prove GA-g-chitosans to be a potent agent when combined with ampicillin and penicillin for the elimination of MRSA.

  17. 21 CFR 177.1060 - n-Alkylglutarimide/acrylic copolymers.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true n-Alkylglutarimide/acrylic copolymers. 177.1060... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1060 n-Alkylglutarimide/acrylic copolymers. n-Alkylglutarimide/acrylic copolymers identified in this section may be safely used as...

  18. 21 CFR 177.1060 - n-Alkylglutarimide/acrylic copolymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false n-Alkylglutarimide/acrylic copolymers. 177.1060... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1060 n-Alkylglutarimide/acrylic copolymers. n-Alkylglutarimide/acrylic copolymers identified in this section may be safely used as...

  19. 21 CFR 177.1060 - n-Alkylglutarimide/acrylic copolymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false n-Alkylglutarimide/acrylic copolymers. 177.1060... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1060 n-Alkylglutarimide/acrylic copolymers. n-Alkylglutarimide/acrylic copolymers identified in this section may be safely used as...

  20. 40 CFR 721.5325 - Nickel acrylate complex.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Nickel acrylate complex. 721.5325... Substances § 721.5325 Nickel acrylate complex. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance nickel acrylate complex (PMN P-85-1034) is subject to reporting...

  1. 40 CFR 721.5325 - Nickel acrylate complex.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Nickel acrylate complex. 721.5325... Substances § 721.5325 Nickel acrylate complex. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance nickel acrylate complex (PMN P-85-1034) is subject to reporting...

  2. 40 CFR 721.5325 - Nickel acrylate complex.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Nickel acrylate complex. 721.5325... Substances § 721.5325 Nickel acrylate complex. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance nickel acrylate complex (PMN P-85-1034) is subject to reporting...

  3. 40 CFR 721.5325 - Nickel acrylate complex.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Nickel acrylate complex. 721.5325... Substances § 721.5325 Nickel acrylate complex. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance nickel acrylate complex (PMN P-85-1034) is subject to reporting...

  4. 21 CFR 175.210 - Acrylate ester copolymer coating.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Acrylate ester copolymer coating. 175.210 Section... COATINGS Substances for Use as Components of Coatings § 175.210 Acrylate ester copolymer coating. Acrylate ester copolymer coating may safely be used as a food-contact surface of articles intended for...

  5. 21 CFR 175.210 - Acrylate ester copolymer coating.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylate ester copolymer coating. 175.210 Section... COATINGS Substances for Use as Components of Coatings § 175.210 Acrylate ester copolymer coating. Acrylate ester copolymer coating may safely be used as a food-contact surface of articles intended for...

  6. 40 CFR 721.329 - Halogenated benzyl ester acrylate (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Halogenated benzyl ester acrylate... Specific Chemical Substances § 721.329 Halogenated benzyl ester acrylate (generic). (a) Chemical substance... halogenated benzyl ester acrylate (PMN P-90-1527) is subject to reporting under this section for...

  7. 40 CFR 721.10180 - Trifunctional acrylic ester (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Trifunctional acrylic ester (generic... Specific Chemical Substances § 721.10180 Trifunctional acrylic ester (generic). (a) Chemical substance and... acrylic ester (PMN P-04-692) is subject to reporting under this section for the significant new...

  8. 40 CFR 721.10180 - Trifunctional acrylic ester (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Trifunctional acrylic ester (generic... Specific Chemical Substances § 721.10180 Trifunctional acrylic ester (generic). (a) Chemical substance and... acrylic ester (PMN P-04-692) is subject to reporting under this section for the significant new...

  9. 40 CFR 721.329 - Halogenated benzyl ester acrylate (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Halogenated benzyl ester acrylate... Specific Chemical Substances § 721.329 Halogenated benzyl ester acrylate (generic). (a) Chemical substance... halogenated benzyl ester acrylate (PMN P-90-1527) is subject to reporting under this section for...

  10. 21 CFR 175.210 - Acrylate ester copolymer coating.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Acrylate ester copolymer coating. 175.210 Section... COATINGS Substances for Use as Components of Coatings § 175.210 Acrylate ester copolymer coating. Acrylate ester copolymer coating may safely be used as a food-contact surface of articles intended for...

  11. 40 CFR 721.329 - Halogenated benzyl ester acrylate (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Halogenated benzyl ester acrylate... Specific Chemical Substances § 721.329 Halogenated benzyl ester acrylate (generic). (a) Chemical substance... halogenated benzyl ester acrylate (PMN P-90-1527) is subject to reporting under this section for...

  12. 40 CFR 721.10180 - Trifunctional acrylic ester (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Trifunctional acrylic ester (generic... Specific Chemical Substances § 721.10180 Trifunctional acrylic ester (generic). (a) Chemical substance and... acrylic ester (PMN P-04-692) is subject to reporting under this section for the significant new...

  13. 21 CFR 175.210 - Acrylate ester copolymer coating.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Acrylate ester copolymer coating. 175.210 Section... COATINGS Substances for Use as Components of Coatings § 175.210 Acrylate ester copolymer coating. Acrylate ester copolymer coating may safely be used as a food-contact surface of articles intended for...

  14. 40 CFR 721.329 - Halogenated benzyl ester acrylate (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Halogenated benzyl ester acrylate... Specific Chemical Substances § 721.329 Halogenated benzyl ester acrylate (generic). (a) Chemical substance... halogenated benzyl ester acrylate (PMN P-90-1527) is subject to reporting under this section for...

  15. 40 CFR 721.10180 - Trifunctional acrylic ester (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Trifunctional acrylic ester (generic... Specific Chemical Substances § 721.10180 Trifunctional acrylic ester (generic). (a) Chemical substance and... acrylic ester (PMN P-04-692) is subject to reporting under this section for the significant new...

  16. 40 CFR 721.10180 - Trifunctional acrylic ester (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Trifunctional acrylic ester (generic... Specific Chemical Substances § 721.10180 Trifunctional acrylic ester (generic). (a) Chemical substance and... acrylic ester (PMN P-04-692) is subject to reporting under this section for the significant new...

  17. 40 CFR 721.10477 - Acrylate ester (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Acrylate ester (generic). 721.10477... Substances § 721.10477 Acrylate ester (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as acrylate ester (PMN P-04-290) is subject...

  18. 40 CFR 721.10477 - Acrylate ester (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Acrylate ester (generic). 721.10477... Substances § 721.10477 Acrylate ester (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as acrylate ester (PMN P-04-290) is subject...

  19. 40 CFR 721.10537 - Acrylate ester (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Acrylate ester (generic). 721.10537... Substances § 721.10537 Acrylate ester (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as acrylate ester (PMN P-01-579) is subject...

  20. 40 CFR 721.10537 - Acrylate ester (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Acrylate ester (generic). 721.10537... Substances § 721.10537 Acrylate ester (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as acrylate ester (PMN P-01-579) is subject...

  1. 40 CFR 721.329 - Halogenated benzyl ester acrylate (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Halogenated benzyl ester acrylate... Specific Chemical Substances § 721.329 Halogenated benzyl ester acrylate (generic). (a) Chemical substance... halogenated benzyl ester acrylate (PMN P-90-1527) is subject to reporting under this section for...

  2. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Acrylate-acrylamide resins. 173.5 Section 173.5... CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.5 Acrylate-acrylamide resins. Acrylate-acrylamide resins may be safely used in food under the following prescribed conditions: (a)...

  3. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Acrylate-acrylamide resins. 173.5 Section 173.5... CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.5 Acrylate-acrylamide resins. Acrylate-acrylamide resins may be safely used in food under the following prescribed conditions: (a)...

  4. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  5. 40 CFR 721.324 - Alkoxylated acrylate polymer (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkoxylated acrylate polymer (generic... Substances § 721.324 Alkoxylated acrylate polymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkoxylated acrylate...

  6. 40 CFR 721.324 - Alkoxylated acrylate polymer (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Alkoxylated acrylate polymer (generic... Substances § 721.324 Alkoxylated acrylate polymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkoxylated acrylate...

  7. 40 CFR 721.324 - Alkoxylated acrylate polymer (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Alkoxylated acrylate polymer (generic... Substances § 721.324 Alkoxylated acrylate polymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkoxylated acrylate...

  8. 40 CFR 721.324 - Alkoxylated acrylate polymer (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Alkoxylated acrylate polymer (generic... Substances § 721.324 Alkoxylated acrylate polymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkoxylated acrylate...

  9. 40 CFR 721.324 - Alkoxylated acrylate polymer (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Alkoxylated acrylate polymer (generic... Substances § 721.324 Alkoxylated acrylate polymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as alkoxylated acrylate...

  10. 40 CFR 721.484 - Fluorinated acrylic copolymer (generic name).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fluorinated acrylic copolymer (generic... Specific Chemical Substances § 721.484 Fluorinated acrylic copolymer (generic name). (a) Chemical substance... fluorinated acrylic copolymer (PMN P-95-1208) is subject to reporting under this section for the...

  11. 40 CFR 721.484 - Fluorinated acrylic copolymer (generic name).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Fluorinated acrylic copolymer (generic... Specific Chemical Substances § 721.484 Fluorinated acrylic copolymer (generic name). (a) Chemical substance... fluorinated acrylic copolymer (PMN P-95-1208) is subject to reporting under this section for the...

  12. 21 CFR 177.1060 - n-Alkylglutarimide/acrylic copolymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false n-Alkylglutarimide/acrylic copolymers. 177.1060... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1060 n-Alkylglutarimide/acrylic copolymers. n-Alkylglutarimide/acrylic copolymers identified in this section may be safely used as...

  13. 21 CFR 177.1320 - Ethylene-ethyl acrylate copolymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ethylene-ethyl acrylate copolymers. 177.1320... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1320 Ethylene-ethyl acrylate copolymers. Ethylene-ethyl acrylate copolymers may be safely used to produce packaging materials,...

  14. 21 CFR 177.1310 - Ethylene-acrylic acid copolymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ethylene-acrylic acid copolymers. 177.1310 Section... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1310 Ethylene-acrylic acid copolymers. The ethylene-acrylic acid copolymers identified in paragraph (a) of this section may be...

  15. 21 CFR 177.1320 - Ethylene-ethyl acrylate copolymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ethylene-ethyl acrylate copolymers. 177.1320... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1320 Ethylene-ethyl acrylate copolymers. Ethylene-ethyl acrylate copolymers may be safely used to produce packaging materials,...

  16. 21 CFR 177.1320 - Ethylene-ethyl acrylate copolymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ethylene-ethyl acrylate copolymers. 177.1320... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1320 Ethylene-ethyl acrylate copolymers. Ethylene-ethyl acrylate copolymers may be safely used to produce packaging materials,...

  17. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  18. 21 CFR 177.1310 - Ethylene-acrylic acid copolymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ethylene-acrylic acid copolymers. 177.1310 Section... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1310 Ethylene-acrylic acid copolymers. The ethylene-acrylic acid copolymers identified in paragraph (a) of this section may be...

  19. 21 CFR 177.1310 - Ethylene-acrylic acid copolymers.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ethylene-acrylic acid copolymers. 177.1310 Section... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1310 Ethylene-acrylic acid copolymers. The ethylene-acrylic acid copolymers identified in paragraph (a) of this section may be...

  20. 21 CFR 177.1310 - Ethylene-acrylic acid copolymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ethylene-acrylic acid copolymers. 177.1310 Section... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1310 Ethylene-acrylic acid copolymers. The ethylene-acrylic acid copolymers identified in paragraph (a) of this section may be...

  1. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylamide-acrylic acid resins. 176.110 Section 176... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  2. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  3. Stainless steel mesh-acrylic cranioplasty.

    PubMed

    Tysvaer, A T; Hovind, K H

    1977-03-01

    Twenty-four steel mesh-acrylic plates have been used for repair of skull defects in 1970-73. Three plates had to be removed due to complications, two due to infection and one due to an allergic reaction. The plate is easy to mould, strong, and light. The cosmetic results are excellent.

  4. 40 CFR 721.2805 - Acrylate ester.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.2805 Acrylate ester. Link to an amendment published at 79 FR 34637, June 18, 2014. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as an...

  5. Acrylic Tanks for Stunning Chemical Demonstrations

    ERIC Educational Resources Information Center

    Mirholm, Alexander; Ellervik, Ulf

    2009-01-01

    We describe the use of acrylic tanks (400 x 450 x 27 mm) for visualization of chemical demonstrations in aqueous solutions. Examples of well-suited demonstrations are oscillating reactions, pH indicators, photochemical reduction of Lauth's violet, and chemoluminiscent reactions. (Contains 1 figure.)

  6. Production of cellulose by Aspergillus niger under submerged and solid state fermentation using coir waste as a substrate

    PubMed Central

    Mrudula, Soma; Murugammal, Rangasamy

    2011-01-01

    Aspergillus niger was used for cellulase production in submerged (SmF) and solid state fermentation (SSF). The maximum production of cellulase was obtained after 72 h of incubation in SSF and 96 h in Smf. The CMCase and FPase activities recorded in SSF were 8.89 and 3.56 U per g of dry mycelial bran (DBM), respectively. Where as in Smf the CMase & FPase activities were found to be 3.29 and 2.3 U per ml culture broth, respectively. The productivity of extracellular cellulase in SSF was 14.6 fold higher than in SmF. The physical and nutritional parameters of fermentation like pH, temperature, substrate, carbon and nitrogen sources were optimized. The optimal conditions for maximum biosynthesis of cellulase by A. niger were shown to be at pH 6, temperature 30 °C. The additives like lactose, peptone and coir waste as substrate increased the productivity both in SmF and SSF. The moisture ratio of 1:2 (w/v) was observed for optimum production of cellulase in SSF. PMID:24031730

  7. Kinetic studies of adsorption of thiocyanate onto ZnCl2 activated carbon from coir pith, an agricultural solid waste.

    PubMed

    Namasivayam, C; Sangeetha, D

    2005-09-01

    The adsorption of thiocyanate onto ZnCl2 activated carbon developed from coir pith was investigated to assess the possible use of this adsorbent. The influence of various parameters such as agitation time, thiocyanate concentration, adsorbent dose, pH and temperature has been studied. Adsorption followed second-order rate kinetics. Two theoretical adsorption isotherms, namely, Langmuir and Freundlich were used to describe the experimental results. The Langmuir adsorption capacity (Q0) was found to be 16.2 mg g(-1) of the adsorbent. The per cent adsorption was maximum in the pH range 3.0-7.0. pH effect and desorption studies showed that ion exchange and chemisorption mechanism are involved in the adsorption process. Thermodynamic parameters such as DeltaG0, DeltaH0 and DeltaS0 for the adsorption were evaluated. The negative values of DeltaH0 confirm the exothermic nature of adsorption. Effects of foreign ions on the adsorption of thiocyanate have been investigated. Removal of thiocyanate from ground water was also tested.

  8. Bioremediation of gasoline contaminated soil by a bacterial consortium amended with poultry litter, coir pith and rhamnolipid biosurfactant.

    PubMed

    Rahman, K S M; Banat, I M; Thahira, J; Thayumanavan, Tha; Lakshmanaperumalsamy, P

    2002-01-01

    The aim of the present study was to find methods for enhancing rates of hydrocarbon biodegradation in gasoline contaminated soil by ex situ bioremediation. Red soil (RS) was treated with gasoline-spilled soil (GS) from a gasoline station and different combinations of amendments were prepared using (i) mixed bacterial consortium (MC), (ii) poultry litter (PL), (iii) coir pith (CP) and (iv) rhamnolipid biosurfactant (BS) produced by Pseudomonas sp. DS10-129. The study was conducted for a period of 90 days during which bacterial growth, hydrocarbon degradation and growth parameters of Phaseolus aureus RoxB including seed germination, chlorophyll content, shoot and root length were measured. Approximately 67% and 78% of the hydrocarbons were effectively degraded within 60 days in soil samples amended with RS + GS + MC + PL + CP + BS at 0.1% and 1%. Maximum percentage of seed germination, shoot length, root length and chlorophyll content in P. aureus were recorded after 60 days in the above amendments. Further incubation to 90 days did not exhibit significant improvements. Statistical analysis using analysis of variance (ANOVA) and Duncan's multiple range test (DMRT) revealed that the level of amendments, incubation time and combination of amendments significantly influenced bacterial growth, hydrocarbon degradation, seed germination and chlorophyll content at a 1% probability level. All tested additives MC, PL, CP and rhamnolipid BS had significant positive effects on the bioremediation of GS.

  9. Removal of chromium(VI) from water and wastewater using surfactant modified coconut coir pith as a biosorbent.

    PubMed

    Namasivayam, C; Sureshkumar, M V

    2008-05-01

    Coconut coir pith, an agricultural solid waste was used as biosorbent for the removal of chromium(VI) after modification with a cationic surfactant, hexadecyltrimethylammonium bromide. Optimum pH for Cr(VI) adsorption was found to be 2.0. Reduction of Cr(VI) to Cr(III) occurred to a slight extent during the removal. Langmuir, Freundlich and Dubinin Radushkevich (D-R) isotherms were used to model the adsorption equilibrium data and the system followed all the three isotherms. The adsorption capacity of the biosorbent was found to be 76.3 mg g(-1), which is higher or comparable to the adsorption capacity of various adsorbents reported in literature. Kinetic studies showed that the adsorption obeyed second order and Elovich model. Thermodynamic parameters such as delta G0, delta H0 and delta S0 were evaluated, indicating that the overall adsorption process was endothermic and spontaneous. Effects of foreign anions were also examined. The adsorbent was also tested for the removal of Cr(VI) from electroplating effluent.

  10. Arsenic(V) removal from aqueous solutions using an anion exchanger derived from coconut coir pith and its recovery.

    PubMed

    Anirudhan, T S; Unnithan, Maya R

    2007-01-01

    The performance of a new anion exchanger (AE) prepared from coconut coir pith (CP), for the removal of arsenic(V) [As(V)] from aqueous solutions was evaluated in this study. The adsorbent (CP-AE) carrying dimethylaminohydroxypropyl weak base functional group was synthesized by the reaction of CP with epichlorohydrin and dimethylamine followed by treatment of hydrochloric acid. IR spectroscopy results confirm the presence of -NH(+)(CH(3))(2)Cl(-) group in the adsorbent. XRD studies confirm the decrease of crystallinity in CP-AE compared to CP, and it favours the protrusion of the functional group into the aqueous medium. Batch experiments were conducted to examine the efficiency of the adsorbent on As(V) removal. Maximum removal of 99.2% was obtained for an initial concentration of 1 mgl(-1) As(V) at pH 7.0 and an adsorbent dose of 2 gl(-1). The kinetics of sorption of As(V) onto CP-AE was described using the pseudo-second-order model. The equilibrium isotherms were determined for different temperatures and the results were analysed using the Langmuir equation. The temperature dependence indicates an exothermic process. Utility of the adsorbent was tested by removing As(V) from simulated groundwater. Regeneration studies were performed using 0.1N HCl. Batch adsorption-desorption studies illustrate that CP-AE could be used to remove As(V) from ground water and other industrial effluents.

  11. Coir geotextile for slope stabilization and cultivation - A case study in a highland region of Kerala, South India

    NASA Astrophysics Data System (ADS)

    Vishnudas, Subha; Savenije, Hubert H. G.; Van der Zaag, Pieter; Anil, K. R.

    A sloping field is not only vulnerable to soil erosion it may also suffer from soil moisture deficiency. Farmers that cultivate on slopes everywhere face similar problems. Conservation technologies may reduce soil and nutrient losses, and thus enhance water holding capacity and soil fertility. But although these technologies promote sustainable crop production on steep slopes, the construction of physical structure such as bench terraces are often labour intensive and expensive to the farmers, since construction and maintenance require high investments. Here we studied the efficiency of coir geotextile with and without crop cultivation in reducing soil moisture deficiency on marginal slopes in Kerala, India. From the results it is evident that the slopes treated with geotextile and crops have the highest moisture retention capacity followed by geotextiles alone, and that the control plot has the lowest moisture retention capacity. As the poor and marginal farmers occupy the highland region, this method provides an economically viable option for income generation and food security along with slope stabilization.

  12. NMR of 129Xe on CO/Ir(1 1 1) and on multilayer Xe/Ir(1 1 1)

    NASA Astrophysics Data System (ADS)

    Koch, Matthias; Gerhard, Peter; Jänsch, Heinz J.

    2006-09-01

    Nuclear magnetic resonance (NMR) is performed on monolayer (ML) amounts of adsorbed 129Xe on a single crystal substrate. The inherently low sensitivity of NMR is overcome by using highly nuclear spin polarized 129Xe that has been produced by optical pumping. A polarization of 0.8 is regularly achieved which is 10 5 times the thermal (Boltzmann) polarization. The experiments are performed with a constant flux of xenon atoms impinging on the surface, typically 4 ML/s. The chemical shift ( σ) of 129Xe is highly sensitive to the Xe local environment. We measured profoundly different shifts for the Xe bulk, for the surface of the Xe bulk, and for Xe on CO/Ir(1 1 1). The growth of the bulk is seen in a phase transition like change of σ as a function of temperature at constant Xe flux. At temperatures where no bulk forms at a flux of 4 ML/s, the xenon exchange rate was measured by a spin inversion/recovery method. The exchange time of Xe is found to be 0.24 s at 63.4 K and 64.4 K and somewhat longer at 61.2 K. An analysis is given involving the desorption out of the second layer and fast mixing of first and second layer atoms at these temperatures.

  13. Physical, Mechanical and Water Absorption Behaviour of Coir Fiber Reinforced Epoxy Composites Filled With Al2O3 Particulates

    NASA Astrophysics Data System (ADS)

    Das, Geetanjali; Biswas, Sandhayarani

    2016-02-01

    The objective of the present work is to study the physical, mechanical and water absorption behaviour of coir fiber reinforced epoxy composites filled with Al2O3 particulates. Composites with different compositions were prepared by varying the length of the fiber and content of fiber using hand lay-up technique. The experimental investigation reveals that the properties of composite increases with the incorporation of Al2O3 particulates. It is observed that the density of composites increases with increase in fiber content, while a decrease in density is observed with increase in fiber length. The strength properties of the composites increases with the increase in fiber content up to 15 wt.% and 12mm fiber length, however further increase in fiber length and fiber content the value decreases. The maximum tensile strength of 25.71MPa, flexural strength of 29.75MPa and impact strength of 14.76kJ/m2 is obtained for composites with 12 mm fiber length and 15 wt.% of fiber content. The hardness and tensile modulus, on the other hand, increases with increase in fiber length and fiber content. The maximum hardness value of 19.52Hv and tensile modulus of 3.412GPa is obtained for composites with 15mm fiber length and 20 wt.% of fiber content. Finally, morphological analysis is also carried out using scanning electron microscope (SEM) to study the fracture behaviour of the composite samples.

  14. Efficient enzymatic acrylation through transesterification at controlled water activity.

    PubMed

    Nordblad, Mathias; Adlercreutz, Patrick

    2008-04-15

    Enzymatic acrylation is a process of potentially strong interest to the chemical industry. Direct esterification involving acrylic acid is unfortunately rather slow, with inhibition phenomena appearing at high acid concentrations. In the present study the acrylation of 1-octanol catalyzed by immobilized Candida antarctica lipase B (Novozym 435) was shown to be as much as an order of magnitude faster when ethyl acrylate served as the donor of the acrylic group. Water activity is a key parameter for optimizing the rate of ester synthesis. The optimum water activity for the esterification of octanol by acrylic acid was found to be 0.75, that for its esterification by propionic acid to be 0.45 and the transesterification involving ethyl acrylate to be fastest at a water activity of 0.3. The reasons for these differences in optimum water activity are discussed in terms of enzyme specificity, substrate solvation, and mass transfer effects.

  15. Large Acrylic Spherical Windows In Hyperbaric Underwater Photography

    NASA Astrophysics Data System (ADS)

    Lones, Joe J.; Stachiw, Jerry D.

    1983-10-01

    Both acrylic plastic and glass are common materials for hyperbaric optical windows. Although glass continues to be used occasionally for small windows, virtually all large viewports are made of acrylic. It is easy to uderstand the wide use of acrylic when comparing design properties of this plastic with those of glass, and glass windows are relatively more difficult to fabricate and use. in addition there are published guides for the design and fabrication of acrylic windows to be used in the hyperbaric environment of hydrospace. Although these procedures for fabricating the acrylic windows are somewhat involved, the results are extremely reliable. Acrylic viewports are now fabricated to very large sizes for manned observation or optical quality instrumen tation as illustrated by the numerous acrylic submersible vehicle hulls for hu, an occupancy currently in operation and a 3600 large optical window recently developed for the Walt Disney Circle Vision under-water camera housing.

  16. Acrylate in Phaeocystis colonies does not affect the surrounding bacteria

    NASA Astrophysics Data System (ADS)

    Noordkamp, D. J. B.; Gieskes, W. W. C.; Gottschal, J. C.; Forney, L. J.; van Rijssel, M.

    2000-08-01

    Acrylate accumulates to concentrations of 1.3-6.5 mM in the mucus of Phaeocystis colonies and may have an effect on the surrounding bacterial community, either as an inhibitor or as a carbon source. Both in the field and in the laboratory, effects of acrylate on bacterial growth and on its consumption were investigated. During a Phaeocystis bloom, acrylate-consuming bacteria were found to be present (1% of total number counted by microscopy) and a 5-fold increase of the number of these bacteria was observed after the Phaeocystis bloom (4.9% of the total number counted by microscopy). Acrylate consumption rates were higher in filtered (≤20 μm) seawater samples than in unfiltered samples, indicating that particles larger than 20 μm, mostly Phaeocystis colonies, caused a reduction in the rate of acrylate consumption. This was not found when axenic Phaeocystis was added to an acrylate-consuming bacterium (strain AC-2) that had been isolated from the highest MPN dilution from field samples. Furthermore, we could not find a decrease in growth rates of the total bacterial community or of isolated strains in the presence of high acrylate concentrations (≤10 mM). In co-cultures of Phaeocystis and strain AC-2 we observed that the production of acrylate was not affected by the bacterium and that the consumption of acrylate by strain AC-2 was not affected by the presence of Phaeocystis. Acrylate concentrations in the mucous layer of the Phaeocystis colonies in those co-cultures were high (6.7-7.7 mM) and comparable with acrylate concentrations in the mucous layer of axenic Phaeocystis colonies. Acrylate seems to be sorbed to the mucus matrix of the colony and diffusion of acrylate out of this mucus matrix appears to be slow. Upon disruption of the colony skin acrylate was immediately solubilised from the mucus matrix.

  17. Self-aggregated nanoparticles based on amphiphilic poly(lactic acid)-grafted-chitosan copolymer for ocular delivery of amphotericin B

    PubMed Central

    Zhou, Wenjun; Wang, Yuanyuan; Jian, Jiuying; Song, Shengfang

    2013-01-01

    Background The purpose of this study was to develop a self-aggregated nanoparticulate vehicle using an amphiphilic poly(lactic acid)-grafted-chitosan (PLA-g-CS) copolymer and to evaluate its potential for ocular delivery of amphotericin B. Methods A PLA-g-CS copolymer was synthesized via a “protection-graft-deprotection” procedure and its structure was confirmed by Fourier transform infrared spectroscopy, 1H nuclear magnetic resonance, and X-ray diffraction spectra. Amphotericin B-loaded nanoparticles based on PLA-g-CS (AmB/PLA-g-CS) were prepared by the dialysis method and characterized for particle size, zeta potential, and encapsulation efficiency. Studies of these AmB/PLA-g-CS nanoparticles, including their mucoadhesive strength, drug release properties, antifungal activity, ocular irritation, ocular pharmacokinetics, and corneal penetration were performed in vitro and in vivo. Results Fourier transform infrared spectroscopy, 1H nuclear magnetic resonance, and X-ray diffraction spectra showed that the PLA chains were successfully grafted onto chitosan molecules and that crystallization of chitosan was suppressed. The self-aggregated PLA-g-CS nanoparticles had a core-shell structure with an average particle size of approximately 200 nm and zeta potentials higher than 30 mV. Amphotericin B was incorporated into the hydrophobic core of the nanoparticles with high encapsulation efficiency. Sustained drug release from the nanoparticles was observed in vitro. The ocular irritation study showed no sign of irritation after instillation of the PLA-g-CS nanoparticles into rabbit eyes. The minimal inhibitory concentration of the AmB/PLA-g-CS nanoparticles showed antifungal activity similar to that of free amphotericin B against Candida albicans. The in vivo ocular pharmacokinetic study suggested that the PLA-g-CS nanoparticles have the advantage of prolonging residence time at the ocular surface. The corneal penetration study showed that the PLA-g-CS nanoparticles

  18. Cycloolefin effect in cycloolefin-(meth)acryl copolymer

    NASA Astrophysics Data System (ADS)

    Lim, Hyun Soon; Seo, Dong Chul; Lee, Chang Soo; Park, Sang Wok; Kim, Sang Jin; Shin, Dae Hyeon; Shin, Jin Bong; Park, Joo Hyun

    2008-11-01

    One of the most important factors in ArF resist development is a resin platform, which dominates a lot of parts of resist characteristics. It has been much changed in order to improve their physical properties such as resolution, pattern profile, etch resistance and line edge roughness. Through the low etch resistance in ArF initial (meth)acryl type copolymer and low transmittance in COMA type copolymer most researchers were interested in developing of (meth)acryl type copolymer again for ArF photoresist. On the other hand, we have studied various polymer platforms suitable ArF photoresist except for meth(acryl) type copolymer. As a result of this study we had developed ROMA type polymers and cycloolefin-(meth)acryl type copolymers. Among the polymers cycloolefin-(meth)acryl type copolymer has many attractions such as etch roughness, resist reflow which needs low glass transition temperature and solvent solubility. In this study, we intend to find out cycloolefin-(meth)acryl copolymer characteristics compared with (meth)acryl copolymer. And, we have tried to find out any differences between acrylate type copolymer and cycloolefin-(meth)acrylate type copolymer with various evaluation results. As a result of this study we are going to talk about the reason that the resist using acrylate type copolymer and cycloolefin-(meth)acryl type copolymer show good pattern profile while acrylate type copolymer show poor pattern profile. We also intend to explain the role of cycloolefin as a function of molecular weight variation and substitution ratio variation of cycloolefin in cycloolefin-(meth)acrylate resin.One of the most important factors in ArF resist development is a resin platform, which dominates a lot of parts of resist characteristics. It has been much changed in order to improve their physical properties such as resolution, pattern profile, etch resistance and line edge roughness. Through the low etch resistance in ArF initial (meth)acryl type copolymer and low

  19. Allergic contact dermatitis from acrylic nails in a flamenco guitarist.

    PubMed

    Alcántara-Nicolás, F A; Pastor-Nieto, M A; Sánchez-Herreros, C; Pérez-Mesonero, R; Melgar-Molero, V; Ballano, A; De-Eusebio, E

    2016-12-01

    Acrylates are molecules that are well known for their strong sensitizing properties. Historically, many beauticians and individuals using store-bought artificial nail products have developed allergic contact dermatitis from acrylates. More recently, the use of acrylic nails among flamenco guitarists to strengthen their nails has become very popular. A 40-year-old non-atopic male patient working as a flamenco guitarist developed dystrophy, onycholysis and paronychia involving the first four nails of his right hand. The lesions were confined to the fingers where acrylic materials were used in order to strengthen his nails to play the guitar. He noticed improvement whenever he stopped using these materials and intense itching and worsening when he began reusing them. Patch tests were performed and positive results obtained with 2-hydroxyethyl methacrylate (2-HEMA), 2-hydroxyethyl acrylate (2-HEA), ethyleneglycol-dimethacrylate (EGDMA) and 2-hydroxypropyl methacrylate (2-HPMA). The patient was diagnosed with occupational allergic contact dermatitis likely caused by acrylic nails. Artificial nails can contain many kinds of acrylic monomers but most cases of contact dermatitis are induced by 2-HEMA, 2-HPMA and EGDMA. This is the first reported case of occupational allergic contact dermatitis from acrylates in artificial nails in a professional flamenco guitar player. Since the practice of self-applying acrylic nail products is becoming very popular within flamenco musicians, we believe that dermatology and occupational medicine specialists should be made aware of the potentially increasing risk of sensitization from acrylates in this setting.

  20. Multiple Internal Reflections in Acrylic Triangle Waveguide

    NASA Astrophysics Data System (ADS)

    Marzuki, A.; Setiawan, D.; Purwanto, H.; Yunianto, M.

    2016-11-01

    Theoretical and experimental study of light propagation in acrylic triangle waveguides has been studied theoretically and experimentally aimed to obtain a light cone which can tunnel and bring the light to a certain place. Numerical aperture of light cones which have a length of 7 cm but different cross-section area have been measured using he-Ne laser (λ=632 nm) and the results were compared to those obtained theoretically and no significant different was observed.

  1. 'Weightless' acrylic painting by Jack Kroehnke

    NASA Technical Reports Server (NTRS)

    1987-01-01

    'Weightless' acrylic painting by Jack Kroehnke depicts STS-26 Discovery, Orbiter Vehicle (OV) 103, Mission Specialist (MS) David C. Hilmers participating in extravehicular activity (EVA) simulation in JSC Weightless Environment Training Facility (WETF) Bldg 29. In the payload bay (PLB) mockup, Hilmers, wearing extravehicular mobility unit (EMU), holds onto the mission-peculiar equipment support structure in foreground while SCUBA-equipped diver monitors activity overhead and camera operator records EVA procedures. Copyrighted art work for use by NASA.

  2. Protein adsorption, fibroblast activity and antibacterial properties of poly(3-hydroxybutyric acid-co-3-hydroxyvaleric acid) grafted with chitosan and chitooligosaccharide after immobilized with hyaluronic acid.

    PubMed

    Hu, S-G; Jou, C-H; Yang, M C

    2003-07-01

    Poly(3-hydroxybutyric acid-co-3-hydroxyvaleric acid) (PHBV) membrane was treated with ozone and grafted with acrylic acid. The resulting membranes were further grafted with chitosan (CS) or chitooligosaccharide (COS) via esterification. Afterward hyaluronic acid (HA) was immobilized onto CS- or COS-grafting membranes. The antibacterial activity of CS and COS against Staphylococus aureus, Escherichia coli, and Pseudomonas aeruginosa was preserved after HA immobilization. Among them, CS-grafted PHBV membrane showed higher antibacterial activity than COS-grafted PHBV membrane. In addition, after CS- or COS-grafting, the L929 fibroblasts attachment and protein adsorption were improved, while the cell number was decrease. After immobilizing HA, the cell proliferation was promoted, the protein adsorption was decreased, and the cell attachment was slightly lower than CS- or COS-grafting PHBV.

  3. Modeling the free radical polymerization of acrylates

    NASA Astrophysics Data System (ADS)

    Günaydin, Hakan; Salman, Seyhan; Tüzün, Nurcan Şenyurt; Avci, Duygu; Aviyente, Viktorya

    Acrylates have gained importance because of their ease of conversion to high-molecular-weight polymers and their broad industrial use. Methyl methacrylate (MMA) is a well-known monomer for free radical polymerization, but its α-methyl substituent restricts the chemical modification of the monomer and therefore the properties of the resulting polymer. The presence of a heteroatom in the methyl group is known to increase the polymerizability of MMA. Methyl α-hydroxymethylacrylate (MHMA), methyl α-methoxymethylacrylate (MC1MA), methyl α-acetoxymethylacrylate (MAcMA) show even better conversions to high-molecular-weight polymers than MMA. In contrast, the polymerization rate is known to decrease as the methyl group is replaced by ethyl in ethyl α-hydroxymethylacrylate (EHMA) and t-butyl in t-butyl α-hydroxymethylacrylate (TBHMA). In this study, quantum mechanical tools (B3LYP/6-31G*) have been used in order to understand the mechanistic behavior of the free radical polymerization reactions of acrylates. The polymerization rates of MMA, MHMA, MC1MA, MAcMA, EHMA, TBHMA, MC1AN (α-methoxymethyl acrylonitrile), and MC1AA (α-methoxymethyl acrylic acid) have been evaluated and rationalized. Simple monomers such as allyl alcohol (AA) and allyl chloride (AC) have also been modeled for comparative purposes.

  4. UV-curable polyurethane acrylate coatings with different acrylate monomers as reactive diluents

    SciTech Connect

    Nabeth, B.; Gerard, J.F.; Pascault, J.P.

    1995-12-01

    Two series of UV-curable polyurethane acrylate (PUA) based on polycaprolactone (PCL), tetraxylylene diisocyanate (TMXDI), and hydroxyethyl acrylate (HEA) or hydroxyethyl methacrylate (HEMA) were studied. These ones were considered with different acrylates as reactive diluents. The effect of the chemical nature and functionality of the reactive diluents on the thermal and dynamic mechanical properties (DMS) was investigated. From a thermodynamic point of view, the PUA seem to display a one phase structure by DMS. Nevertheless, the statistic heterogeneities due to the use of three monomers or more can explain the Tg values and the mechanical relaxations of the PUA. The Tg-onset of the PUA is slightly influenced by the nature of the reactive diluents but is dependent on the Tg of the oligomer confirming the description of the structure using a clusters model. The same conclusions could be done from the dynamic mechanical spectra of the PUA sandwiched and UV-cured between two glass plates.

  5. Mercury(II) removal from aqueous solutions and wastewaters using a novel cation exchanger derived from coconut coir pith and its recovery.

    PubMed

    Anirudhan, T S; Divya, L; Ramachandran, M

    2008-09-15

    A new adsorbent (PGCP-COOH) having carboxylate functional group at the chain end was synthesized by grafting poly(hydroxyethylmethacrylate) onto coconut coir pith, CP (a coir industry-based lignocellulosic residue), using potassium peroxydisulphate as an initiator and in the presence of N,N'-methylenebisacrylamide as a cross-linking agent. The adsorbent was characterized with the help of infrared spectroscopy, powder X-ray diffraction, scanning electron microscopy, and potentiometric titrations. The ability of PGCP-COOH to remove Hg(II) from aqueous solutions was assessed using batch adsorption technique under kinetic and equilibrium conditions. Adsorbent exhibits very high adsorption potential for Hg(II) and more than 99.0% removal was achieved in the pH range 5.5-8.0. Adsorption process was found to follow first-order-reversible kinetics. An increase of ionic strength of the medium caused a decrease in metal removal, indicating the occurrence of outer-sphere surface complex mechanism. The equilibrium data were fitted well by the Freundlich isotherm model (R(2)=0.99; chi(2)=1.81). The removal efficiency was tested using chlor-alkali industry wastewater. Adsorption isotherm experiments were also conducted for comparison using a commercial carboxylate-functionalized ion exchanger, Ceralite IRC-50. Regeneration experiments were tried for four cycles and results indicate a capacity loss of <9.0%.

  6. Palladium (II) catalyized polymerization of norbornene and acrylates

    DOEpatents

    Sen, Ayusman; Kacker, Smita; Hennis, April; Polley, Jennifer D.

    2000-08-29

    Homopolymers or copolymers of acrylates, homopolymers or copolymers of norbornenes, and copolymers of acrylates with norbornenes, may be prepared by contacting acrylate and/or norbornene monomer reactant under polymerization conditions and in the presence of a solvent with a catalyst system consisting essentially of a Pd(II) dimer component having the formula: [(L)Pd(R)(X)].sub.2, where L is a monodentate phosphorus or nitrogen ligand, X is an anionic group, and R is an alkyl or aryl group.

  7. Palladium (Ii) Catalyzed Polymerization Of Norbornene And Acrylates

    DOEpatents

    Sen, Ayusman; Kacker, Smita; Hennis, April; Polley, Jennifer D.

    2001-10-09

    Homopolymers or copolymers of acrylates, homopolymers or copolymers of norbornenes, and copolymers of acrylates with norbornenes, may be prepared by contacting acrylate and/or norbornene monomer reactant under polymerization conditions and in the presence of a solvent with a catalyst system consisting essentially of a Pd(II) dimer component having the formula: where L is a monodentate phosphorus or nitrogen ligand, X is an anionic group, and R is an alkyl or aryl group.

  8. Improved Acrylic Systems for Rapid Runway Repair.

    DTIC Science & Technology

    1983-05-01

    Concrete * Fast-Setting Concrete N Acrylic Polymer Research * 1 k UST mACV lC@ea. ON -- -0 - OW. 00....Y d*Ip OF 40 domb) The objectives of this...available to the general public, including foreign nationals. This technical report has been reviewed and is approved for publication. DANIEL J. PIERRE, Capt...resins. The aggregate and resin might be premixed for placement or (as in the research reported herein) the cap might be formed by percolation of liquid

  9. Ocean Engineering Studies. Volume 1. Acrylic Submersibles

    DTIC Science & Technology

    1990-04-01

    the tie rods is larger than the forces applied to the hatch system P ..eYe during lifting, the joints in the acrylic plastic hull will never be...and MI L- P -21 I 05C materials. 22 elastomeric spacers to _______ allow free contraction . of the hull under pressure topper cape ring u~.Chairs...to tie rods Clearance between fi..forrgdyatce and hull to allow free con. to support frame traction of bull under p ensur *oft support frame rigidly

  10. Comparison of Candida Albicans Adherence to Conventional Acrylic Denture Base Materials and Injection Molding Acrylic Materials

    PubMed Central

    Aslanimehr, Masoomeh; Rezvani, Shirin; Mahmoudi, Ali; Moosavi, Najmeh

    2017-01-01

    Statement of the Problem: Candida species are believed to play an important role in initiation and progression of denture stomatitis. The type of the denture material also influences the adhesion of candida and development of stomatitis. Purpose: The aim of this study was comparing the adherence of candida albicans to the conventional and injection molding acrylic denture base materials. Materials and Method: Twenty injection molding and 20 conventional pressure pack acrylic discs (10×10×2 mm) were prepared according to their manufacturer’s instructions. Immediately before the study, samples were placed in sterile water for 3 days to remove residual monomers. The samples were then sterilized using an ultraviolet light unit for 10 minutes. 1×108 Cfu/ml suspension of candida albicans ATCC-10231 was prepared from 48 h cultured organism on sabouraud dextrose agar plates incubated at 37oC. 100 μL of this suspension was placed on the surface of each disk. After being incubated at 37oC for 1 hour, the samples were washed with normal saline to remove non-adherent cells. Attached cells were counted using the colony count method after shaking at 3000 rmp for 20 seconds. Finally, each group was tested for 108 times and the data were statistically analyzed by t-test. Results: Quantitative analysis revealed that differences in colony count average of candida albicans adherence to conventional acrylic materials (8.3×103) comparing to injection molding acrylic resins (6×103) were statistically significant (p<0.001). Conclusion: Significant reduction of candida albicans adherence to the injection acrylic resin materials makes them valuable for patients with high risk of denture stomatitis. PMID:28280761

  11. 40 CFR 721.8082 - Polyester polyurethane acrylate.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polyester polyurethane acrylate. 721... Substances § 721.8082 Polyester polyurethane acrylate. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyester polyurethane...

  12. 40 CFR 721.8082 - Polyester polyurethane acrylate.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Polyester polyurethane acrylate. 721... Substances § 721.8082 Polyester polyurethane acrylate. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyester polyurethane...

  13. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.5 Acrylate-acrylamide resins... and acrylic acid, with the greater part of the polymer being composed of acrylamide units. (2) Sodium... sodium silicate-sodium hydroxide aqueous solution, with the greater part of the polymer being composed...

  14. The Acrylation of Glycerol: a Precursor to Functionalized Lipids

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Didecanoylacryloylglycerol was synthesized from decanoic and acrylic acids and glycerol using K2O as catalyst. This reaction was carried out in hexane in a closed stainless steel reactor at 200°C for 5h. The reactants were added in a 1:3:4 glycerol:decanoic acid:acrylic acid molar ratio. The resu...

  15. 40 CFR 721.10500 - Acrylated mixed metal oxides (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Acrylated mixed metal oxides (generic... Specific Chemical Substances § 721.10500 Acrylated mixed metal oxides (generic). (a) Chemical substance and... mixed metal oxides (PMN P-06-341) is subject to reporting under this section for the significant...

  16. 40 CFR 721.10500 - Acrylated mixed metal oxides (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Acrylated mixed metal oxides (generic... Specific Chemical Substances § 721.10500 Acrylated mixed metal oxides (generic). (a) Chemical substance and... mixed metal oxides (PMN P-06-341) is subject to reporting under this section for the significant...

  17. Instrumental Characterization Of Coir PITH By XRD, FTIR and SEM After Radium Adsorption From Aqueous Solution Under The Presence Of Humic Acids

    NASA Astrophysics Data System (ADS)

    Laili, Zalina; Omar, Muhamat; Yasir, Muhamad Samudi; Ibrahim, Mohd Zaidi; Yahaya, Mohd Yusri; Murshidi, Julie Andrianny

    2010-01-01

    Adsorption interactions of radium (Ra) ions onto coir pith (CP) under the presence of humic acid (HA) in the aqueous solution were investigated using X-ray diffraction (XRD), Fourier Transform Infrared Spectrophotometer (FTIR) and Scanning Electron Microscopy (SEM) techniques. XRD, IR and SEM characterization of the CP has revealed differences in the native CP and Ra ions loaded CP under the presence of HA in the aqueous solution. The X-Ray patterns showed that crystalline structure of the loaded CP exhibited a decrease in crystalline structure at around 49°-51° compared with unloaded CP. Characterization by IR revealed that participation of some surface functional groups during the Ra adsorption. SEM images for the morphological studies showed that there were slightly changes of the CP surfaces after the adsorption process.

  18. Ab initio study of acrylate polymerization reactions: methyl methacrylate and methyl acrylate propagation.

    PubMed

    Yu, Xinrui; Pfaendtner, Jim; Broadbelt, Linda J

    2008-07-24

    The kinetic parameters of the free radical propagation of methyl methacrylate and methyl acrylate have been calculated using quantum chemistry and transition state theory. Multiple density functional theory (DFT) methods were used to calculate the activation energy, and it was found that MPWB1K/6-31G(d,p) yields results that are in very good agreement with experimental data. To obtain values of the kinetic parameters that were in the best agreement with experimental data, low frequencies were treated using a one-dimensional internal rotor model. Chain length effects were also explored by examining addition reactions of monomeric, dimeric, and trimeric radicals to monomer for both methyl methacrylate and methyl acrylate. The results show that the values for the addition of the trimeric radical to monomer are closest to experimental data. The kinetic parameters that were calculated using a continuum description of the monomer as a solvent were not significantly different from the vacuum results.

  19. Synthesis and Characteristics of Radiation Curable Polyurethanes Containing Pendant Acrylate Groups.

    DTIC Science & Technology

    1986-10-09

    the mechanical properties of electron beam . cured acrylated polyester urethanes based on toluene diisocyanate(TDI) and hydroxyethyl - methacrylate ( HEMA ...acrylate or methacrylate pendant groups are can- didates for radiation sensitive solid polymers since the acrylate groups may undergo crosslinking...acrylate com- 4ponents. Toluene diisocyanate - hydroxyethylmethacrylate (TDI- HEMA ) or isophorone diisocyanate - hydroxylethylmethacrylate (IPDI-HEHA

  20. Electrochemical characterization of aminated acrylic conducting polymer

    SciTech Connect

    Rashid, Norma Mohammad; Heng, Lee Yook; Ling, Tan Ling

    2015-09-25

    New attempt has been made to synthesize aminated acrylic conducting polymer (AACP) using precursor of phenylvinylsulfoxide (PVS). The process was conducted via the integration of microemulsion and photopolymerization techniques. It has been utilized for covalent immobilization of amino groups by the adding of N-achryiloxisuccinimide (NAS). Thermal eliminating of benzene sulfenic acids from PVS has been done at 250 °C to form electroactive polyacetylene (PA) segment. Characterization of AACP has been conducted using fourier transform infrared (FTIR), scanning electron microscopy (SEM) and linear sweep cyclic voltammetry (CV). A range of 0.3-1.25μm particle size obtained from SEM characterization. A quasi-reversible system performed as shown in electrochemical study.

  1. Flexible, stretchable electroadhesives based on acrylic elastomers

    NASA Astrophysics Data System (ADS)

    Duduta, Mihai; Wood, Robert J.; Clarke, David R.

    2016-04-01

    Controllable adhesion is a requirement for a wide variety of applications including robotic manipulation, as well as locomotion including walking, crawling and perching. Electroadhesives have several advantages such as reversibility, low power consumption and controllability based on applied voltage. Most demonstrations of electroadhesive devices rely on fairly rigid materials, which cannot be stretched reversibly, as needed in some applications. We have developed a fast and reliable method for building soft, stretchable electroadhesive pads based on acrylic elastomers and electrodes made of carbon nanotubes. The devices produced were tested pre-deformation and in a stretched configuration. The adhesive force was determined to be in the 0.1 - 3.0 N/cm2 range, depending on the adhering surface. The electroadhesive devices were integrated with pre-stretched dielectric elastomer actuators to create a device in which the adhesion force could be tuned by changes in either the applied voltage or total area.

  2. Conversion of Lignocellulosic Biomass to Ethanol and Butyl Acrylate

    SciTech Connect

    Binder, Thomas; Erpelding, Michael; Schmid, Josef; Chin, Andrew; Sammons, Rhea; Rockafellow, Erin

    2015-04-10

    Conversion of Lignocellulosic Biomass to Ethanol and Butyl Acrylate. The purpose of Archer Daniels Midlands Integrated Biorefinery (IBR) was to demonstrate a modified acetosolv process on corn stover. It would show the fractionation of crop residue to distinct fractions of cellulose, hemicellulose, and lignin. The cellulose and hemicellulose fractions would be further converted to ethanol as the primary product and a fraction of the sugars would be catalytically converted to acrylic acid, with butyl acrylate the final product. These primary steps have been demonstrated.

  3. Methods for the synthesis of deuterated acrylate salts

    SciTech Connect

    Yang, Jun; Bonnesen, Peter V.; Hong, Kunlun

    2014-09-09

    A method for synthesizing a deuterated acrylate of the Formula (1), the method comprising: (i) deuterating a propiolate compound of Formula (2) to a methyne-deuterated propiolate compound of Formula (3) in the presence of a base and D.sub.2O: and (ii) reductively deuterating the methyne-deuterated propiolate compound of Formula (3) in a reaction solvent in the presence of deuterium gas and a palladium-containing catalyst to afford the deuterated acrylate of the Formula (1). The resulting deuterated acrylate compounds, derivatives thereof, and polymers derived therefrom are also described.

  4. Investigation of Acrylic Acid at High Pressure Using Neutron Diffraction

    PubMed Central

    2014-01-01

    This article details the exploration of perdeuterated acrylic acid at high pressure using neutron diffraction. The structural changes that occur in acrylic acid-d4 are followed via diffraction and rationalized using the Pixel method. Acrylic acid undergoes a reconstructive phase transition to a new phase at ∼0.8 GPa and remains molecular to 7.2 GPa before polymerizing on decompression to ambient pressure. The resulting product is analyzed via Raman and FT-IR spectroscopy and differential scanning calorimetry and found to possess a different molecular structure compared with polymers produced via traditional routes. PMID:24650085

  5. Performance behavior of modified cellulosic fabrics using polyurethane acrylate copolymer.

    PubMed

    Zuber, Mohammad; Shah, Sayyed Asim Ali; Jamil, Tahir; Asghar, Muhammad Irfan

    2014-06-01

    The surface of the cellulosic fabrics was modified using self-prepared emulsions of polyurethane acrylate copolymers (PUACs). PUACs were prepared by varying the molecular weight of polycaprolactone diol (PCL). The PCL was reacted with isophorone diisocyanate (IPDI) and chain was extended with 2-hydroxy ethyl acrylate (HEA) to form vinyl terminated polyurethane (VTPU) preploymer. The VTPU was further co-polymerized through free radical polymerization with butyl acrylate in different proportions. The FT-IR spectra of monomers, prepolymers and copolymers assured the formation of proposed PUACs structure. The various concentrations of prepared PUACs were applied onto the different fabric samples using dip-padding techniques. The results revealed that the application of polyurethane butyl acrylate copolymer showed a pronounced effect on the tear strength and pilling resistance of the treated fabrics.

  6. Emulsion Polymerization of Butyl Acrylate: Spin Trapping and EPR Study

    NASA Technical Reports Server (NTRS)

    Kim, S.; Westmoreland, D.

    1994-01-01

    The propagating radical in the emulsion polymerization reaction of butyl acrylate was detected by Electron Paramagnetic Resonance spectroscopy using two spin trapping agents, 2-methyl-2nitrosopropane and alpha -N-tert-butylnitrone.

  7. Use of acrylic sheet molds for elastomeric products

    NASA Technical Reports Server (NTRS)

    Heisman, R. M.; Koerner, A. E.; Messineo, S. M.

    1970-01-01

    Molds constructed of acrylic sheet are more easily machined than metal, are transparent to ensure complete filling during injection, and have smooth surfaces free of contamination. Technique eliminates flashing on molded parts and mold release agents.

  8. Acrylamide/acrylic acid copolymers for cement fluid loss control

    SciTech Connect

    McKenzie, L.F.; McElfresh, P.M.

    1982-01-01

    Acrylamide/acrylic acid copolymers are considered as effective fluid loss control additives in a wide range of oil well cements. Unlike HEC based fluid loss aditives, these copolymers can be used with calcium chloride accelerator without significantly influencing fluid loss control. Another advantage of the copolymers is that the amount of fluid loss for a given concentration of polymer remains relatively constant over a wide range of temperatures. The use of acrylamide/acrylic acid copolymers has generally been restricted to wells below 60 degree C BHCT. Above that temperature chemical changes in the copolymer often lead to retardation of the cement. This paper presents data related to the use of acrylamide/acrylic acid copolymers as fluid loss control agents in oil well cementing. A comparison of these polymers with HEC based fluid loss control additives is made. In addition, data related to the cause of acrylamide/acrylic acid copolymer retarding effects is presented. 4 refs.

  9. Thermophysical properties of fluorinated acrylate homopolymers: Mixing and phase separation

    NASA Astrophysics Data System (ADS)

    Roussel, F.; Saidi, S.; Guittard, F.; Geribaldi, S.

    2002-06-01

    The thermophysical properties of fluorinated acrylate homopolymers are investigated by differential scanning calorimetry (DSC) and optical microscopy and discussed in terms of relative lengths of the fluorinated chain and the hydrocarbon spacer between the acrylate moiety and the fluorinated chain. These compounds exhibit an intrinsic microphase-separation (Isotropic+Isotropic morphology) occurring between the fluorinated chains and the acrylate polymer backbone. It is shown that the enthalpy of mixing is a function of the length of the lateral fluorocarbon chains. The thermophysical behaviour of these materials may be regarded as demixed systems exhibiting an Upper Critical Solution Temperature. The photopolymerization process of one of the monomer is studied by isothermal photocalorimetry. High acrylate double-bond conversion and fast curing rates were obtained thus demonstrating the promising use of these materials for coating and film processing applications using UV-curing techniques.

  10. PERMEATION OF MULTIFUNCTIONAL ACRYLATES THROUGH SELECTED PROTECTIVE GLOVE MATERIALS

    EPA Science Inventory

    In support of the Premanufacture Notification (PMN) program of the Environmental Protection Agency's Office of Toxic Substances, the resistance of three glove materials to permeation by multifunctional acrylate compounds was evaluated through a program for the Office of Research ...

  11. Fabrication of interim acrylic resin removable partial dentures with clasps.

    PubMed

    Reitz, P V; Weiner, M G

    1978-12-01

    An orderly sequence of steps for construction of an interim acrylic resin partial denture has been presented. The technique allows the dentist to fabricate an effective restoration that has a definite path of insertion and removal that can be placed in the patient's mouth with little time spent on adjustment and correction. This technique may be used with heat- or cold-curing acrylic resin.

  12. Poly(meth)acrylates obtained by cascade reaction.

    PubMed

    Popescu, Dragos; Keul, Helmut; Moeller, Martin

    2011-04-04

    Preparation, purification, and stabilization of functional (meth)acrylates with a high dipole moment are complex, laborious, and expensive processes. In order to avoid purification and stabilization of the highly reactive functional monomers, a concept of cascade reactions was developed comprising enzymatic monomer synthesis and radical polymerization. Transacylation of methyl acrylate (MA) and methyl methacrylate (MMA) with different functional alcohols, diols, and triols (1,2,6-hexanetriol and glycerol) in the presence of Novozyme 435 led to functional (meth)acrylates. After the removal of the enzyme by means of filtration, removal of excess (meth)acrylate and/or addition of a new monomer, e.g., 2-hydroxyethyl (meth)acrylate the (co)polymerization via free radical (FRP) or nitroxide mediated radical polymerization (NMP) resulted in poly[(meth)acrylate]s with predefined functionalities. Hydrophilic, hydrophobic as well as ionic repeating units were assembled within the copolymer. The transacylation of MA and MMA with diols and triols carried out under mild conditions is an easy and rapid process and is suitable for the preparation of sensitive monomers.

  13. Stabilizing effects of estertins mercaptide (methyl acrylate) for PVC degradation

    NASA Astrophysics Data System (ADS)

    Zhang, S. H.; Liu, T. M.; Li, J. L.; Wang, C. R.; Li, C.; Wang, Z. Q.

    2016-07-01

    The thermal and UV light (ultraviolet light) stability of PVC films with estertins mercaptide (methyl acrylate), methyltins mercaptide and the compound consisted of estertins mercaptide (methyl acrylate) and hydrotalcite (2:2.5) were investigated by ageing in a circulation oven at 190 °C and irradiating with 72W UV light for 96h, respectively, and then the yellowness and transmission rate were tested by Color Quest XE. Hydrotalcite was proved to have good synergies with estertins mercaptide (methyl acrylate) on improving the thermal stability and UV light stability. The retarding effects of the heat stabilizers to PVC degradation were tested by TGA from 50°C to 600°C. The results show that temperature of HCl evolution from PVC film was improved obviously by compounding with estertins mercaptide(methyl acrylate) and hydrotalcite and estertins mercaptide(methyl acrylate) was found to have a better long term stability. Sn4+ consistence of water and seawater in which films before and after UV light irradiation were soaked for 60 days was analyzed by ICP; the results indicate that the Sn4+ consistence from the films with estertins mercaptide(methyl acrylate) as thermal stabilizer was lower than that from the film with methyltins mercaptide. The crosslink moderately by UV irradiation for PVC films can hold back the dissolution of organotin heat stabilizers from PVC products into water and seawater.

  14. Advances in acrylic-alkyd hybrid synthesis and characterization

    NASA Astrophysics Data System (ADS)

    Dziczkowski, Jamie

    2008-10-01

    In situ graft acrylic-alkyd hybrid resins were formed by polymerizing acrylic and acrylic-mixed monomers in the presence of alkyds by introduction of a free radical initiator to promote graft formation. Two-dimensional NMR, specifically gradient heteronuclear multiple quantum coherence (gHMQC), was used to clarify specific graft sites of the hybrid materials. Both individual and mixed-monomer systems were produced to determine any individual monomer preferences and to model current acrylic-alkyd systems. Different classes of initiators were used to determine any initiator effects on graft location. The 2D-NMR results confirm grafting at doubly allylic hydrogens located on the fatty acid chains and the polyol segment of the alkyd backbone. The gHMQC spectra show no evidence of grafting across double bonds on either pendant fatty acid groups or THPA unsaturation sites for any of the monomer or mixed monomer systems. It was also determined that choice of initiator has no effect on graft location. In addition, a design of experiments using response surface methodology was utilized to obtain a better understanding of this commercially available class of materials and relate both the chemical and physical properties to one another. A Box-Behnkin design was used, varying the oil length of the alkyd phase, the degree of unsaturation in the polyester backbone, and acrylic to alkyd ratio. Acrylic-alkyd hybrid resins were reduced with an amine/water mixture. Hydrolytic stability was tested and viscoelastic properties were obtained to determine crosslink density. Cured films were prepared and basic coatings properties were evaluated. It was found that the oil length of the alkyd is the most dominant factor for final coatings properties of the resins. Acrylic to alkyd ratio mainly influences the resin properties such as acid number, average molecular weight, and hydrolytic stability. The degree of unsaturation in the alkyd backbone has minimal effects on resin and film

  15. Analysis of emulsion stability in acrylic dispersions

    NASA Astrophysics Data System (ADS)

    Ahuja, Suresh

    2012-02-01

    Emulsions either micro or nano permit transport or solubilization of hydrophobic substances within a water-based phase. Different methods have been introduced at laboratory and industrial scales: mechanical stirring, high-pressure homogenization, or ultrasonics. In digital imaging, toners may be formed by aggregating a colorant with a latex polymer formed by batch or semi-continuous emulsion polymerization. Latex emulsions are prepared by making a monomer emulsion with monomer like Beta-carboxy ethyl acrylate (β-CEA) and stirring at high speed with an anionic surfactant like branched sodium dodecyl benzene sulfonates , aqueous solution until an emulsion is formed. Initiator for emulsion polymerization is 2-2'- azobis isobutyramide dehydrate with chain transfer agent are used to make the latex. If the latex emulsion is unstable, the resulting latexes produce a toner with larger particle size, broader particle size distribution with relatively higher latex sedimentation, and broader molecular weight distribution. Oswald ripening and coalescence cause droplet size to increase and can result in destabilization of emulsions. Shear thinning and elasticity of emulsions are applied to determine emulsion stability.

  16. Large deformation micromechanics of particle filled acrylics at elevated temperatures

    NASA Astrophysics Data System (ADS)

    Gunel, Eray Mustafa

    The main aim of this study is to investigate stress whitening and associated micro-deformation mechanism in thermoformed particle filled acrylic sheets. For stress whitening quantification, a new index was developed based on image histograms in logarithmic scale of gray level. Stress whitening levels in thermoformed acrylic composites was observed to increase with increasing deformation limit, decreasing forming rate and increasing forming temperatures below glass transition. Decrease in stress whitening levels above glass transition with increasing forming temperature was attributed to change in micro-deformation behavior. Surface deformation feature investigated with scanning electron microscopy showed that source of stress whitening in thermoformed samples was a combination of particle failure and particle disintegration depending on forming rate and temperature. Stress whitening level was strongly correlated to intensity of micro-deformation features. On the other hand, thermoformed neat acrylics displayed no surface discoloration which was attributed to absence of micro-void formation on the surface of neat acrylics. Experimental damage measures (degradation in initial, secant, unloading modulus and strain energy density) have been inadequate in describing damage evolution in successive thermoforming applications on the same sample at different levels of deformation. An improved version of dual-mechanism viscoplastic material model was proposed to predict thermomechanical behavior of neat acrylics under non-isothermal conditions. Simulation results and experimental results were in good agreement and failure of neat acrylics under non-isothermal conditions ar low forming temperatures were succesfully predicted based on entropic damage model. Particle and interphase failure observed in acrylic composites was studied in a multi-particle unit cell model with different volume fractions. Damage evolution due to particle failure and interphase failure was simulated

  17. Purification and characterisation of processive-type endoglucanase and β-glucosidase from Aspergillus ochraceus MTCC 1810 through saccharification of delignified coir pith to glucose.

    PubMed

    Asha, P; Divya, Jose; Bright Singh, I S

    2016-08-01

    The study describes purification and characterisation of processive-type endoglucanase and β-glucosidase from Aspergillus ochraceus MTCC 1810 through bioconversion of delignified coir pith to fermentable glucose. The purified processive endoglucanase (AS-HT-Celuz A) and β-glucosidase (AS-HT-Celuz B) were found to have molecular mass of ≈78-kDa and 43-kDa respectively with optimum endoglucanase (35.63U/ml), total cellulase (28.15FPU/ml) and β-glucosidase (15.19U/ml) activities at 40°C/pH 6. The unique feature of AS-HT-Celuz A is the multiple substrate specificity and processivity towards both amorphous and crystalline cellulose. Zymogram indicated both endo and exoglucanase activities residing in different binding sites of a single protein exhibiting sequential synergy with its own β-glucosidase. Accordingly, the identified enzymes could be implemented as synergistic cellulases for complete cellulose saccharification which still considered an unresolved issue in bio-refineries.

  18. Biocatalytic functionalization of hydroxyalkyl acrylates and phenoxyethanol via phosphorylation.

    PubMed

    Tasnádi, Gábor; Hall, Mélanie; Baldenius, Kai; Ditrich, Klaus; Faber, Kurt

    2016-09-10

    The enzymatic phosphorylation of phenoxyethanol, 2-hydroxyethyl acrylate and 4-hydroxybutyl acrylate catalyzed by acid phosphatases PhoN-Sf and PiACP at the expense of inorganic di-, tri-, hexameta- or polyphosphate was applied to the preparative-scale synthesis of phosphorylated compounds. The reaction conditions were optimized with respect to enzyme immobilization, substrate concentration, pH and type of phosphate donor. The mild reaction conditions prevented undesired polymerization and hydrolysis of the acrylate ester moiety. Application of a continuous flow system allowed facile scale-up and mono-phosphates were obtained in up to 26% isolated yield with space-time yields of 0.89kgL(-1)h(-1).

  19. Allergic contact stomatitis caused by acrylic monomer in a denture.

    PubMed

    Koutis, D; Freeman, S

    2001-08-01

    A 71-year-old edentulous man developed a severely painful red mouth at sites of contact with a new denture. Patch testing showed allergy to samples of the denture material and to 2-hydroxyethyl methacrylate. Patch testing to methyl methacrylate was negative. Prolonged boiling of the denture resulted in reversal of his symptoms and samples of this fully cured denture material produced negative patch tests. While allergy to acrylates is a rare cause of stomatitis, this possibility must be considered in patients presenting with oral symptoms. Material safety data sheets are unreliable in providing information regarding the type of acrylate present in the material. Hence, patch testing should be performed with a battery of acrylate allergens as well as with small samples of the denture material.

  20. Effect of Cigarette Smoke on Acrylic Resin Teeth

    PubMed Central

    Patil, Seema S.; M.R., Dhakshaini; Gujjari, Anil Kumar

    2013-01-01

    Background: The discolouration of artificial teeth, which hampers aesthetics, is one of the negative effects of cigarette smoking. Therefore, the effect of cigarette smoke on the colour stability of commercially available acrylic resin teeth needs to be evaluated for clinical success and to ascertain as to which brand has superior properties. Material and Methods: Three commercially available acrylic teeth were evaluated, after division into Group A (Premadent), Group B (Astra), and Group C (Sanyo- Dent). Selected brands were subdivided as study group and control group. Each set of acrylic resin teeth were stored in artificial saliva at 37±1°C for 24 hours. After 24 hours of immersion, the colour measurement of each tooth (T0) was performed. Second colour measurements were done after 21 days (T21) of exposure to cigarette smoke for study group and after immersion in artificial saliva for control group. All data was statistically analyzed by using Repeated Measures ANOVA and Two-way ANOVA (p<0.05). Results: Group A showed least total colour change on exposure to cigarette smoke, followed by Group B and Group C had the highest total colour change. In control group, after immersion in artificial saliva, a slight increase in total colour change was observed for all groups, which was clinically acceptable. Conclusion: Group A (crosslinked acrylic resin teeth) was more colour stable and more resistant to the discolouration which was caused by cigarette smoke, followed by Group B (crosslinked acrylic resin teeth). Group C (Non-crosslinked acrylic resin teeth) was least colour stable and most susceptible to discolouration which was caused by cigarette smoke. PMID:24179942

  1. Colour Stability of Heat and Cold Cure Acrylic Resins

    PubMed Central

    Ganesh, P R; Reddy, Madan Mohan; Ebenezar, A.V. Rajesh; Sivakumar, G

    2015-01-01

    Introduction: To evaluate the colour stability of heat and cold cure acrylic resins under simulated oral conditions with different colorants. Materials and Methods: Three different brands of heat cure acrylic resin and two rapid cure auto polymerizing acrylic resin of commercial products such as Trevelon Heat Cure (THC), DPI Heat cure (DHC), Pyrax Heat Cure (PHC), DPI Cold cure (DCC) and Acralyn-R-Cold cure (ACC) have been evaluated for discoloration and colour variation on subjecting it to three different, commonly employed food colorants such as Erythrosine, Tartarizine and Sunset yellow. In order to simulate the oral condition the food colorants were diluted with artificial saliva to the samples taken up for the study. These were further kept in an incubator at 37°C ± 1°C. The UV-visible spectrophotometer has been utilized to evaluate the study on the basis of CIE L* a* b* system. The prepared samples for standard evaluation have been grouped as control group, which has been tested with a white as standard, which is applicable for testing the colour variants. Results: The least colour changes was found to be with Sunset Yellow showing AE* value of 3.55 with heat cure acrylic resin branded as PHC material and the highest colour absorption with Tartarizine showing AE* value of 12.43 in rapid cure autopolymerzing acrylic resin material branded as ACC material. Conclusion: ACC which is a self cure acrylic resin shows a higher colour variation to the tartarizine food coloration. There were not much of discoloration values shown on the denture base resins as the food colorants are of organic azodyes. PMID:25738078

  2. The creep behavior of acrylic denture base resins.

    PubMed

    Sadiku, E R; Biotidara, F O

    1996-01-01

    The creep behavior of acrylic dental base resins, at room temperature and at different loading conditions, has been examined. The behaviors of these resins are similar to that of "commercial perspex" at room temperature over a period of 1000 seconds. The pseudo-elastic moduli of the blends of PMMA VC show a significant increase compared with PMMA alone. The addition of the PVC powder to the heat-cured acrylic resin increased the time-dependent elastic modulus. This increase in elastic modulus is advantageous in the production of denture based resins of improv mechanical properties.

  3. Lipase-catalyzed aza-Michael reaction on acrylate derivatives.

    PubMed

    Steunenberg, Peter; Sijm, Maarten; Zuilhof, Han; Sanders, Johan P M; Scott, Elinor L; Franssen, Maurice C R

    2013-04-19

    A methodology has been developed for an efficient and selective lipase-catalyzed aza-Michael reaction of various amines (primary and secondary) with a series of acrylates and alkylacrylates. Reaction parameters were tuned, and under the optimal conditions it was found that Pseudomonas stutzeri lipase and Chromobacterium viscosum lipase showed the highest selectivity for the aza-Michael addition to substituted alkyl acrylates. For the first time also, some CLEAs were examined that showed a comparable or higher selectivity and yield than the free enzymes and other formulations.

  4. 40 CFR 721.338 - Salt of an acrylate copolymer (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Salt of an acrylate copolymer (generic... Substances § 721.338 Salt of an acrylate copolymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substances identified generically as salt of an acrylate...

  5. 40 CFR 721.338 - Salt of an acrylate copolymer (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Salt of an acrylate copolymer (generic... Substances § 721.338 Salt of an acrylate copolymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substances identified generically as salt of an acrylate...

  6. 40 CFR 180.1162 - Acrylate polymers and copolymers; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 25 2013-07-01 2013-07-01 false Acrylate polymers and copolymers... RESIDUES IN FOOD Exemptions From Tolerances § 180.1162 Acrylate polymers and copolymers; exemption from the requirement of a tolerance. (a) Acrylate polymers and copolymers are exempt from the requirement of...

  7. 40 CFR 721.10192 - Amides, coco, N-[3-(dibutylamino)propyl], acrylates.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Amides, coco, N- , acrylates. 721... Substances § 721.10192 Amides, coco, N- , acrylates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amides, coco, N- , acrylates (PMN...

  8. 40 CFR 721.10192 - Amides, coco, N-[3-(dibutylamino)propyl], acrylates.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Amides, coco, N- , acrylates. 721... Substances § 721.10192 Amides, coco, N- , acrylates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amides, coco, N- , acrylates (PMN...

  9. 40 CFR 721.10192 - Amides, coco, N-[3-(dibutylamino)propyl], acrylates.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Amides, coco, N- , acrylates. 721... Substances § 721.10192 Amides, coco, N- , acrylates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amides, coco, N- , acrylates (PMN...

  10. 40 CFR 721.10192 - Amides, coco, N-[3-(dibutylamino)propyl], acrylates.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Amides, coco, N- , acrylates. 721... Substances § 721.10192 Amides, coco, N- , acrylates. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as amides, coco, N- , acrylates (PMN...

  11. 40 CFR 721.321 - Substituted acrylamides and acrylic acid copolymer (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Substituted acrylamides and acrylic... New Uses for Specific Chemical Substances § 721.321 Substituted acrylamides and acrylic acid copolymer... identified generically as substituted acrylamides and acrylic acid copolymer (PMN P-00-0490) is subject...

  12. 40 CFR 721.321 - Substituted acrylamides and acrylic acid copolymer (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Substituted acrylamides and acrylic... New Uses for Specific Chemical Substances § 721.321 Substituted acrylamides and acrylic acid copolymer... identified generically as substituted acrylamides and acrylic acid copolymer (PMN P-00-0490) is subject...

  13. 40 CFR 721.321 - Substituted acrylamides and acrylic acid copolymer (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Substituted acrylamides and acrylic... New Uses for Specific Chemical Substances § 721.321 Substituted acrylamides and acrylic acid copolymer... identified generically as substituted acrylamides and acrylic acid copolymer (PMN P-00-0490) is subject...

  14. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  15. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  16. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  17. 40 CFR 721.321 - Substituted acrylamides and acrylic acid copolymer (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Substituted acrylamides and acrylic... New Uses for Specific Chemical Substances § 721.321 Substituted acrylamides and acrylic acid copolymer... identified generically as substituted acrylamides and acrylic acid copolymer (PMN P-00-0490) is subject...

  18. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  19. 40 CFR 721.321 - Substituted acrylamides and acrylic acid copolymer (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Substituted acrylamides and acrylic... New Uses for Specific Chemical Substances § 721.321 Substituted acrylamides and acrylic acid copolymer... identified generically as substituted acrylamides and acrylic acid copolymer (PMN P-00-0490) is subject...

  20. 40 CFR 721.9640 - Salt of an acrylic acid - acrylamide terpolymer (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Salt of an acrylic acid - acrylamide... Specific Chemical Substances § 721.9640 Salt of an acrylic acid - acrylamide terpolymer (generic). (a... generically as salt of an acrylic acid - acrylamide terpolymer (PMN P-99-817) is subject to reporting...

  1. 40 CFR 721.338 - Salt of an acrylate copolymer (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Salt of an acrylate copolymer (generic... Substances § 721.338 Salt of an acrylate copolymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substances identified generically as salt of an acrylate...

  2. 40 CFR 721.338 - Salt of an acrylate copolymer (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Salt of an acrylate copolymer (generic... Substances § 721.338 Salt of an acrylate copolymer (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substances identified generically as salt of an acrylate...

  3. 40 CFR 721.6560 - Acrylic acid, polymer with substituted ethene.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.6560 Acrylic acid, polymer with substituted ethene. (a) Chemical... as acrylic acid, polymer with substituted ethene (PMN P-91-521) is subject to reporting under...

  4. 40 CFR 721.6920 - Butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Butyl acrylate, polymer with... acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted silane. (a... butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

  5. 40 CFR 180.1162 - Acrylate polymers and copolymers; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 24 2011-07-01 2011-07-01 false Acrylate polymers and copolymers... RESIDUES IN FOOD Exemptions From Tolerances § 180.1162 Acrylate polymers and copolymers; exemption from the requirement of a tolerance. (a) Acrylate polymers and copolymers are exempt from the requirement of...

  6. 40 CFR 721.10032 - Acrylic acid, polymer with substituted acrylamides (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.10032 Acrylic acid, polymer with substituted acrylamides (generic). (a... generically as acrylic acid, polymer with substituted acrylamides (PMN P-02-269) is subject to reporting...

  7. 40 CFR 721.6560 - Acrylic acid, polymer with substituted ethene.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.6560 Acrylic acid, polymer with substituted ethene. (a) Chemical... as acrylic acid, polymer with substituted ethene (PMN P-91-521) is subject to reporting under...

  8. 40 CFR 721.6560 - Acrylic acid, polymer with substituted ethene.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.6560 Acrylic acid, polymer with substituted ethene. (a) Chemical... as acrylic acid, polymer with substituted ethene (PMN P-91-521) is subject to reporting under...

  9. 40 CFR 721.6920 - Butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Butyl acrylate, polymer with... acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted silane. (a... butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

  10. 40 CFR 180.1162 - Acrylate polymers and copolymers; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 24 2014-07-01 2014-07-01 false Acrylate polymers and copolymers... RESIDUES IN FOOD Exemptions From Tolerances § 180.1162 Acrylate polymers and copolymers; exemption from the requirement of a tolerance. (a) Acrylate polymers and copolymers are exempt from the requirement of...

  11. 40 CFR 721.10032 - Acrylic acid, polymer with substituted acrylamides (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.10032 Acrylic acid, polymer with substituted acrylamides (generic). (a... generically as acrylic acid, polymer with substituted acrylamides (PMN P-02-269) is subject to reporting...

  12. 40 CFR 721.6920 - Butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Butyl acrylate, polymer with... acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted silane. (a... butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

  13. 40 CFR 721.6560 - Acrylic acid, polymer with substituted ethene.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.6560 Acrylic acid, polymer with substituted ethene. (a) Chemical... as acrylic acid, polymer with substituted ethene (PMN P-91-521) is subject to reporting under...

  14. 40 CFR 721.10223 - Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... ferrite with acrylic ester polymer (generic). 721.10223 Section 721.10223 Protection of Environment... manganese ferrite with acrylic ester polymer (generic). (a) Chemical substance and significant new uses... manganese ferrite with acrylic ester polymer (PMN P-09-582) is subject to reporting under this section...

  15. 40 CFR 721.10032 - Acrylic acid, polymer with substituted acrylamides (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.10032 Acrylic acid, polymer with substituted acrylamides (generic). (a... generically as acrylic acid, polymer with substituted acrylamides (PMN P-02-269) is subject to reporting...

  16. 40 CFR 721.463 - Acrylate of polymer based on isophorone diisocyanate (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Acrylate of polymer based on... New Uses for Specific Chemical Substances § 721.463 Acrylate of polymer based on isophorone... substance identified generically as acrylate of polymer based on isophorone diisocyanate (PMN P-00-0626)...

  17. 40 CFR 721.463 - Acrylate of polymer based on isophorone diisocyanate (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Acrylate of polymer based on... New Uses for Specific Chemical Substances § 721.463 Acrylate of polymer based on isophorone... substance identified generically as acrylate of polymer based on isophorone diisocyanate (PMN P-00-0626)...

  18. 40 CFR 721.10032 - Acrylic acid, polymer with substituted acrylamides (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.10032 Acrylic acid, polymer with substituted acrylamides (generic). (a... generically as acrylic acid, polymer with substituted acrylamides (PMN P-02-269) is subject to reporting...

  19. 40 CFR 721.6920 - Butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Butyl acrylate, polymer with... acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted silane. (a... butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

  20. 40 CFR 721.10223 - Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... ferrite with acrylic ester polymer (generic). 721.10223 Section 721.10223 Protection of Environment... manganese ferrite with acrylic ester polymer (generic). (a) Chemical substance and significant new uses... manganese ferrite with acrylic ester polymer (PMN P-09-582) is subject to reporting under this section...

  1. 40 CFR 721.463 - Acrylate of polymer based on isophorone diisocyanate (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Acrylate of polymer based on... New Uses for Specific Chemical Substances § 721.463 Acrylate of polymer based on isophorone... substance identified generically as acrylate of polymer based on isophorone diisocyanate (PMN P-00-0626)...

  2. 40 CFR 180.1162 - Acrylate polymers and copolymers; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Acrylate polymers and copolymers... RESIDUES IN FOOD Exemptions From Tolerances § 180.1162 Acrylate polymers and copolymers; exemption from the requirement of a tolerance. (a) Acrylate polymers and copolymers are exempt from the requirement of...

  3. 40 CFR 721.10223 - Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... ferrite with acrylic ester polymer (generic). 721.10223 Section 721.10223 Protection of Environment... manganese ferrite with acrylic ester polymer (generic). (a) Chemical substance and significant new uses... manganese ferrite with acrylic ester polymer (PMN P-09-582) is subject to reporting under this section...

  4. 40 CFR 721.463 - Acrylate of polymer based on isophorone diisocyanate (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Acrylate of polymer based on... New Uses for Specific Chemical Substances § 721.463 Acrylate of polymer based on isophorone... substance identified generically as acrylate of polymer based on isophorone diisocyanate (PMN P-00-0626)...

  5. 40 CFR 721.6560 - Acrylic acid, polymer with substituted ethene.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.6560 Acrylic acid, polymer with substituted ethene. (a) Chemical... as acrylic acid, polymer with substituted ethene (PMN P-91-521) is subject to reporting under...

  6. 40 CFR 721.6920 - Butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Butyl acrylate, polymer with... acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted silane. (a... butyl acrylate, polymer with substituted methyl styrene, methyl methacrylate, and substituted...

  7. 40 CFR 721.463 - Acrylate of polymer based on isophorone diisocyanate (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Acrylate of polymer based on... New Uses for Specific Chemical Substances § 721.463 Acrylate of polymer based on isophorone... substance identified generically as acrylate of polymer based on isophorone diisocyanate (PMN P-00-0626)...

  8. 40 CFR 180.1162 - Acrylate polymers and copolymers; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 25 2012-07-01 2012-07-01 false Acrylate polymers and copolymers... RESIDUES IN FOOD Exemptions From Tolerances § 180.1162 Acrylate polymers and copolymers; exemption from the requirement of a tolerance. (a) Acrylate polymers and copolymers are exempt from the requirement of...

  9. 40 CFR 721.10032 - Acrylic acid, polymer with substituted acrylamides (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Acrylic acid, polymer with substituted... Specific Chemical Substances § 721.10032 Acrylic acid, polymer with substituted acrylamides (generic). (a... generically as acrylic acid, polymer with substituted acrylamides (PMN P-02-269) is subject to reporting...

  10. 40 CFR 721.10223 - Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... ferrite with acrylic ester polymer (generic). 721.10223 Section 721.10223 Protection of Environment... manganese ferrite with acrylic ester polymer (generic). (a) Chemical substance and significant new uses... manganese ferrite with acrylic ester polymer (PMN P-09-582) is subject to reporting under this section...

  11. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ethylene-methyl acrylate copolymer resins. 177.1340... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1340 Ethylene-methyl acrylate copolymer resins. Ethylene-methyl acrylate copolymer resins may be safely used as articles or components...

  12. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ethylene-methyl acrylate copolymer resins. 177... for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1340 Ethylene-methyl acrylate copolymer resins. Ethylene-methyl acrylate copolymer resins may be safely used...

  13. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ethylene-methyl acrylate copolymer resins. 177... for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1340 Ethylene-methyl acrylate copolymer resins. Ethylene-methyl acrylate copolymer resins may be safely used...

  14. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ethylene-methyl acrylate copolymer resins. 177... Repeated Use Food Contact Surfaces § 177.1340 Ethylene-methyl acrylate copolymer resins. Ethylene-methyl... section, the ethylene-methyl acrylate copolymer resins consist of basic copolymers produced by...

  15. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ethylene-methyl acrylate copolymer resins. 177... for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1340 Ethylene-methyl acrylate copolymer resins. Ethylene-methyl acrylate copolymer resins may be safely used...

  16. Tensile bond strength between auto-polymerized acrylic resin and acrylic denture teeth treated with MF-MA solution

    PubMed Central

    2016-01-01

    PURPOSE This study evaluated the effect of chemical surface treatment using methyl formate-methyl acetate (MF-MA) solution on the tensile bond strength between acrylic denture teeth and auto-polymerized acrylic resin. MATERIALS AND METHODS Seventy maxillary central incisor acrylic denture teeth for each of three different brands (Yamahachi New Ace; Major Dent; Cosmo HXL) were embedded with incisal edge downwards in auto-polymerized resin in polyethylene pipes and ground with silicone carbide paper on their ridge lap surfaces. The teeth of each brand were divided into seven groups (n=10): no surface treatment (control group), MF-MA solution at a ratio of 25:75 (v/v) for 15 seconds, 30 seconds, 60 seconds, 120 seconds, 180 seconds, and MMA for 180 seconds. Auto-polymerized acrylic resin (Unifast Trad) was applied to the ground surface and polymerized in a pressure cooker. A tensile strength test was performed with a universal testing machine. Statistical analysis of the results was performed using two-way analysis of variance (ANOVA) and post-hoc Dunnett T3 test (α=.05). RESULTS The surface treatment groups had significantly higher mean tensile bond strengths compared with the control group (P<.05) when compared within the same brand. Among the surface treatment groups of each brand, there were no significantly different tensile bond strengths between the MF-MA groups and the MMA 180 second group (P>.05), except for the Yamahachi New Ace MF-MA 180-second group (P<.05). CONCLUSION 15-second MF-MA solution can be an alternative chemical surface treatment for repairing a denture base and rebonding acrylic denture teeth with auto-polymerized acrylic resin, for both conventional and cross-linked teeth. PMID:27555897

  17. Acrylic resin injection method for blood vessel investigations.

    PubMed

    Suwa, Fumihiko; Uemura, Mamoru; Takemura, Akimichi; Toda, Isumi; Fang, Yi-Ru; Xu, Yuan Jin; Zhang, Zhi Yuan

    2013-01-01

    The injection of acrylic resin into vessels is an excellent method for macroscopically and microscopically observing their three-dimensional features. Conventional methods can be enhanced by removal of the polymerization inhibitor (hydroquinone) without requiring distillation, a consistent viscosity of polymerized resin, and a constant injection pressure and speed. As microvascular corrosion cast specimens are influenced by viscosity, pressure, and speed changes, injection into different specimens yields varying results. We devised a method to reduce those problems. Sodium hydroxide was used to remove hydroquinone from commercial methylmethacrylate. The solid polymer and the liquid monomer were mixed using a 1 : 9 ratio (low-viscosity acrylic resin, 9.07 ± 0.52 mPa•s) or a 3:7 ratio (high-viscosity resin, 1036.33 ± 144.02 mPa•s). To polymerize the acrylic resin for injection, a polymerization promoter (1.0% benzoyl peroxide) was mixed with a polymerization initiator (0.5%, N, N-dimethylaniline). The acrylic resins were injected using a precise syringe pump, with a 5-mL/min injection speed and 11.17 ± 1.60 mPa injection pressure (low-viscosity resin) and a 1-mL/min injection speed and 58.50 ± 5.75 mPa injection pressure (high-viscosity resin). Using the aforementioned conditions, scanning electron microscopy indicated that sufficient resin could be injected into the capillaries of the microvascular corrosion cast specimens.

  18. Interactions of sodium montmorillonite with poly(acrylic acid).

    PubMed

    Tran, Nguyen H; Dennis, Gary R; Milev, Adriyan S; Kannangara, G S Kamali; Wilson, Michael A; Lamb, Robert N

    2005-10-15

    The chemical-structural modifications of the natural clay sodium montmorillonite during interaction with poly(acrylic acid) were studied mainly by X-ray photoemission spectroscopy. Samples of modified montmorillonite were prepared from the reaction of sodium montmorillonite ( approximately 0.5 g) and an aqueous solution of poly(acrylic acid) (pH approximately 1.8, 50 g) at varying temperatures. X-ray diffraction indicated that the montmorillonite interlayer space ( approximately 13 A), formed by regular stacking of the silicate layers (dimension approximately 1x1000 nm), expanded to approximately 16 A as the reaction was carried out at room temperature and at 30 degrees C. At 60 degrees C, the interlayer space further expanded to approximately 20 A. The results of X-ray photoemission spectroscopy indicated that poly(acrylic acid) molecules exchange sodium ions on the surface of the silicate layers. These combined results allowed development of a reaction model that explains the dependency of the interlayer expansion with temperature. Information concerning the surface chemical reactions and systematic increases in the interlayer distances is particularly useful if montmorillonite and poly(acrylic acid) are to be used for formation of nanocomposite materials.

  19. Mid-infrared laser ablation of intraocular acrylic lenses

    NASA Astrophysics Data System (ADS)

    Spyratou, E.; Makropoulou, M.; Bacharis, C.; Serafetinides, A. A.

    2007-05-01

    Ablation rates measurements with free-running Er:YAG laser (λ=2.94 μm) were performed in hydrophilic acrylic intraocular lenses. We studied the role of water in the laser ablation mechanisms by using hydrophilic lenses with different concentrations of H II0 and D II0. A mathematical model simulated the experimental results.

  20. 21 CFR 177.1320 - Ethylene-ethyl acrylate copolymers.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... blended with polyethylene or with one or more olefin copolymers complying with § 177.1520 or with a mixture of polyethylene and one or more olefin copolymers, in such proportions that the ethyl acrylate... prescribed in paragraph (c)(2) of this section, when tested by the methods prescribed for polyethylene...

  1. JKR studies of adhesion with model acrylic elastomers

    SciTech Connect

    Shull, K.R.; Ahn, D.

    1996-12-31

    Acrylic elastomers are widely used in coating applications because of their inherent thermal stability, oil resistance and adhesive properties. These same features make acrylic elastomers attractive for fundamental studies of polymer adhesion. This endeavor has been simplified recently by the development of techniques for producing monodisperse acrylic homopolymers and block copolymers from anionically synthesized parent polyacrylates, thus allowing precise microstructural control of adhering surfaces. In terms of the adhesion measurement itself, an adhesion test based upon the theory of Johnson, Kendall and Roberts (JKR), henceforth referred to as the JKR technique, is well suited for probing the molecular origins of adhesion in elastomeric systems. This technique is quite practical, and minimizes the sample volume to reduce bulk viscoelastic losses. Further, the JKR technique permits testing at very low crack velocities, where interfacial effects are unobscured by bulk effects. In this paper, the authors report the results of JKR adhesion tests between poly(n-butyl acrylate) (PNBA) elastomers and poly(methyl methacrylate) (PMMA). The latter is employed as a control substrate because its inertness and low surface energy (relative to metallic or silicon based surfaces) are conducive to the creation of reproducible solid surfaces.

  2. Humidity-responsive starch-poly (methyl acrylate) films.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Blown films prepared from starch-poly(methyl acrylate) graft copolymers plasticized with urea and water display shrinkage at relative humidities greater than 50%. Shrinkage at relative humidities below approximately 75% is strongly correlated with the urea/starch weight ratio, which controls the eq...

  3. 40 CFR 721.5325 - Nickel acrylate complex.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.5325 Nickel acrylate complex. Link to an amendment published at 79 FR 34637, June 18, 2014. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical...

  4. Acrylic acid and electric power cogeneration in an SOFC reactor.

    PubMed

    Ji, Baofeng; Wang, Jibo; Chu, Wenling; Yang, Weishen; Lin, Liwu

    2009-04-21

    A highly efficient catalyst, MoV(0.3)Te(0.17)Nb(0.12)O, used for acrylic acid (AA) production from propane, was used as an anodic catalyst in an SOFC reactor, from which AA and electric power were cogenerated at 400-450 degrees C.

  5. Antimicrobial activity of poly(acrylic acid) block copolymers.

    PubMed

    Gratzl, Günther; Paulik, Christian; Hild, Sabine; Guggenbichler, Josef P; Lackner, Maximilian

    2014-05-01

    The increasing number of antibiotic-resistant bacterial strains has developed into a major health problem. In particular, biofilms are the main reason for hospital-acquired infections and diseases. Once formed, biofilms are difficult to remove as they have specific defense mechanisms against antimicrobial agents. Antimicrobial surfaces must therefore kill or repel bacteria before they can settle to form a biofilm. In this study, we describe that poly(acrylic acid) (PAA) containing diblock copolymers can kill bacteria and prevent from biofilm formation. The PAA diblock copolymers with poly(styrene) and poly(methyl methacrylate) were synthesized via anionic polymerization of tert-butyl acrylate with styrene or methyl methacrylate and subsequent acid-catalyzed hydrolysis of the tert-butyl ester. The copolymers were characterized via nuclear magnetic resonance spectroscopy (NMR), size-exclusion chromatography (SEC), Fourier transform infrared spectroscopy (FTIR), elemental analysis, and acid-base titrations. Copolymer films with a variety of acrylic acid contents were produced by solvent casting, characterized by atomic force microscopy (AFM) and tested for their antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. The antimicrobial activity of the acidic diblock copolymers increased with increasing acrylic acid content, independent of the copolymer-partner, the chain length and the nanostructure.

  6. Sensitization capacity of acrylated prepolymers in ultraviolet curing inks tested in the guinea pig.

    PubMed

    Björkner, B

    1981-01-01

    One commonly used prepolymer in ultraviolet (UV) curing inks is epoxy acrylate. Of 6 men with dermatitis contracted from UV-curing inks, 2 had positive patch test reaction to epoxy acrylate. None reacted to the chemically related bisphenol A dimethacrylate. The sensitization capacity of epoxy acrylate and bisphenol A dimethacrylate performed with the "Guinea pig maximization test" (GPM) shows epoxy acrylate to be an extreme sensitizer and bisphenol A dimethacrylate a moderate sensitizer. Cross-reaction between the two substances occurs. The epoxy resin oligomer MW 340 present in the epoxy acrylate also sensitized some animals.

  7. Synthesis and Characterization of Polyurethane Acrylates for UV Curable Coating Agents

    NASA Astrophysics Data System (ADS)

    Park, Mi Na; Kang, Young Soo; Oh, Sun Wha; Ahn, Byung Hyun; Moon, Myung Jun

    The single hydroxyl-terminated urethane acrylate oligomers were synthesized from 2-mercaptoethanol (2-MEOH), alkyl (methyl, butyl, and 2-ethylhexyl) acrylate, and 2,2-azobisisobutyronitrile (AIBN, initiator), with dibutyltin dilaurate (DBTDL) as a catalyst. 2-MEOH was used as a functional chain transfer agent. Poly(alkyl urethane) acrylate oligomers were obtained by the reaction of single hydroxyl-terminated polyalkyl acrylates and 2-isocyanatoethyl acrylate. They were characterized by NMR, FT-IR spectroscopy, rheometer, and DSC. Because poly(alkyl urethane) acrylate oligomers have lower Tg and viscosity than hydroxyl-terminated polyalkyl acrylate oligomers (HTPAO) non-containing urethane groups, they can be used for ultraviolet (UV) curable coatings, inks, and adhesives.

  8. Wavelength Shifters and Interactions of EDTA with Acrylic & LAB

    NASA Astrophysics Data System (ADS)

    Mohan, Yuvraj; SNO+ Collaboration

    2014-09-01

    The SNO + experiment, an upgrade to the Sudbury Neutrino Observatory, will use linear alkyl-benzene (LAB) liquid scintillator to probe new physics, including 0 νββ decay. Event detection efficiency is heavily affected by radioactive backgrounds, two sources being Rn-222 and Po-210 daughters, some of which has become embedded in the SNO + acrylic vessel after years underground. The leading candidate for polonium leaching is Ethylenediaminetetraacetic acid (EDTA). Before deployment on-site, EDTA's effects on the mechanical integrity of acrylic must be determined. It also must not be soluble in LAB or must be removed before scintillator fill of the vessel, as its presence would result in reduced light yield due to scattering. It was found that EDTA had negligible effects on the Young's Modulus of acrylic. EDTA is also slightly soluble in LAB, but can be completely removed by rinsing with water. Additionally, the study of the light yield and alpha/beta timing profiles of two wavelength shifters - bisMSB and perylene - is critical to determining which should be added to the 0 νββ isotope (tellurium) LAB cocktail. Small-scale results hint that perylene might be better, but this is being confirmed with larger-scale tests. The SNO + experiment, an upgrade to the Sudbury Neutrino Observatory, will use linear alkyl-benzene (LAB) liquid scintillator to probe new physics, including 0 νββ decay. Event detection efficiency is heavily affected by radioactive backgrounds, two sources being Rn-222 and Po-210 daughters, some of which has become embedded in the SNO + acrylic vessel after years underground. The leading candidate for polonium leaching is Ethylenediaminetetraacetic acid (EDTA). Before deployment on-site, EDTA's effects on the mechanical integrity of acrylic must be determined. It also must not be soluble in LAB or must be removed before scintillator fill of the vessel, as its presence would result in reduced light yield due to scattering. It was found that EDTA

  9. Polymerization of acrylic acid using atmospheric pressure DBD plasma jet

    NASA Astrophysics Data System (ADS)

    Bashir, M.; Bashir, S.

    2016-08-01

    In this paper polymerization of acrylic acid was performed using non thermal atmospheric pressure plasma jet technology. The goal of this study is to deposit organic functional coatings for biomedical applications using a low cost and rapid growth rate plasma jet technique. The monomer solution of acrylic acid was vaporized and then fed into the argon plasma for coating. The discharge was powered using a laboratory made power supply operating with sinusoidal voltage signals at a frequency of 10 kHz. The optical emission spectra were collected in order to get insight into the plasma chemistry during deposition process. The coatings were characterized using Fourier transform infrared spectroscopy, atomic force microscopy and growth rates analysis. A high retention of carboxylic functional groups of the monomer was observed at the surface deposited using this low power technique.

  10. Reversible opacification of a hydrophilic acrylic intraocular lens.

    PubMed

    Park, Choul Yong; Chuck, Roy S

    2012-01-01

    A 56-year-old woman with diabetic retinopathy and chronic myelogenous leukemia had phacoemulsification cataract removal and hydrophilic acrylic intraocular lens (IOL) (Akreos MI-60) implantation in both eyes. One month after surgery, significant IOL opacity and severe cystoid macular edema were observed in both eyes. After bilateral intravitreal injection of bevacizumab (Avastin) to control macular edema, central clearing of the IOL opacity was observed in both eyes. Two months after the injection, the IOL opacity had almost disappeared from both eyes. To our knowledge, this is the first case of early postoperative bilateral IOL opacity in a hydrophilic acrylic IOL cleared after anti-vascular endothelial growth factor (VEGF) intravitreal injection. The role of anti-VEGF therapy in clearing IOL opacification requires further investigation.

  11. Stronger multilayer acrylic dielectric elastomer actuators with silicone gel coatings

    NASA Astrophysics Data System (ADS)

    Lau, Gih-Keong; La, Thanh-Giang; Sheng-Wei Foong, Ervin; Shrestha, Milan

    2016-12-01

    Multilayer dielectric elastomer actuators (DEA) perform worst off than single-layer DEAs due to higher susceptibility to electro-thermal breakdown. This paper presents a hot-spot model to predict the electro-thermal breakdown field of DEAs and its dependence on thermal insulation. To inhibit the electrothermal breakdown, silicone gel coating was applied as barrier coating to multilayer acrylic DEA. The gel coating helps suppress the electro-thermally induced puncturing of DEA membrane at the hot spot. As a result, the gel-coated DEAs, in either a single layer or a multilayer stack, can produce 30% more isometric stress change as compared to those none-coated. These gel-coated acrylic DEAs show great potential to make stronger artificial muscles.

  12. Corrosion inhibition of reinforcing steel by using acrylic latex

    SciTech Connect

    Wang, S.X.; Lin, W.W.; Ceng, S.A.; Zhang, J.Q.

    1998-05-01

    Acrylic latex was introduced into steel-reinforcing steel concrete as concrete admixtures or rebar coatings in order to prevent corrosion of steel reinforcements. The results showed that applying the latex by both methods took effect in different ways, while the latter was more noticeable. The corrosion prevention mechanism and the surface state of the steel rebar were also explored, based on which suggestions for enhancing the corrosion-resistant ability were made.

  13. Superselective Embolization in Posttraumatic Priapism with Glubran 2 Acrylic Glue

    SciTech Connect

    Gandini, Roberto; Spinelli, Alessio; Konda, Daniel Reale, Carlo Andrea; Fabiano, Sebastiano; Pipitone, Vincenzo; Simonetti, Giovanni

    2004-09-15

    Two patients with posttraumatic priapism underwent transcatheter embolization using microcoils, resulting in temporary penile detumescence and an apparent resolution of the artero-venous fistula. In both cases, priapism recurred 24 hours after the procedure and was successfully treated through selective transcatheter embolization of the nidus using acrylic glue (Glubran 2). The patients showed complete recovery of sexual activity within 30 days from the procedure and persistent exclusion of the artero-venous fistula after a 12-month follow-up.

  14. Acrylic strengthened casts for removable partial denture for occlusion equilibration.

    PubMed

    Oh, Won-Suk; Saglik, Berna

    2011-09-01

    A removable partial denture (RPD) remount cast must resist wear or breakage, present a rigid surface, and ensure a solid support for an accurate equilibration of the occlusion for a RPD. This article describes a procedure of processing a thin layer of tooth colored acrylic resin over the dental plaster to present wear- and fracture-resistant incisal/occlusal surfaces without involving a third material.

  15. Acrylic microspheres-based optosensor for visual detection of nitrite.

    PubMed

    Noor, Nur Syarmim Mohamed; Tan, Ling Ling; Heng, Lee Yook; Chong, Kwok Feng; Tajuddin, Saiful Nizam

    2016-09-15

    A new optosensor for visual quantitation of nitrite (NO2(-)) ion has been fabricated by physically immobilizing Safranine O (SO) reagent onto a self-adhesive poly(n-butyl acrylate) [poly(nBA)] microspheres matrix, which was synthesized via facile microemulsion UV lithography technique. Evaluation and optimization of the optical NO2(-) ion sensor was performed with a fiber optic reflectance spectrophotometer. Scanning electron micrograph showed well-shaped and smooth spherical morphology of the poly(nBA) microspheres with a narrow particles size distribution from 0.6 μm up to 1.8 μm. The uniform size distribution of the acrylic microspheres promoted homogeneity of the immobilized SO reagent molecules on the microspheres' surfaces, thereby enhanced the sensing response reproducibility (<5% RSD) with a linear range obtained from 10 to 100 ppm NO2(-) ion. The micro-sized acrylic immobilization matrix demonstrated no significant barrier for diffusion of reactant and product, and served as a good solid state ion transport medium for reflectometric nitrite determination in food samples.

  16. Epoxy-acrylic core-shell particles by seeded emulsion polymerization.

    PubMed

    Chen, Liang; Hong, Liang; Lin, Jui-Ching; Meyers, Greg; Harris, Joseph; Radler, Michael

    2016-07-01

    We developed a novel method for synthesizing epoxy-acrylic hybrid latexes. We first prepared an aqueous dispersion of high molecular weight solid epoxy prepolymers using a mechanical dispersion process at elevated temperatures, and we subsequently used the epoxy dispersion as a seed in the emulsion polymerization of acrylic monomers comprising methyl methacrylate (MMA) and methacrylic acid (MAA). Advanced analytical techniques, such as scanning transmission X-ray microscopy (STXM) and peak force tapping atomic force microscopy (PFT-AFM), have elucidated a unique core-shell morphology of the epoxy-acrylic hybrid particles. Moreover, the formation of the core-shell morphology in the seeded emulsion polymerization process is primarily attributed to kinetic trapping of the acrylic phase at the exterior of the epoxy particles. By this new method, we are able to design the epoxy and acrylic polymers in two separate steps, and we can potentially synthesize epoxy-acrylic hybrid latexes with a broad range of compositions.

  17. Research of morphology structure and properties of bamboo charcoal acrylic fiber

    NASA Astrophysics Data System (ADS)

    Zhang, Yongjiu; Feng, Aifen

    2015-07-01

    In order to understand the properties of bamboo charcoal acrylic fiber, the tensile properties, friction properties and hygroscopicity of it, the bamboo charcoal acrylic fiber and the ordinary acrylic fiber were tested, compared and analyzed. The burning behaviors of the two kinds of fibers were observed by burning test, and their cross-sectional and longitudinal morphology was observed with scanning electron microscope (SEM). The SEM pictures showed that there are the uneven sizes of microspores on the surface of bamboo charcoal acrylic fiber and in it. It was found that the friction coefficients of the bamboo charcoal acrylic fiber are smaller and its tensile and moisture absorption are better than those of the ordinary acrylic fiber. However, there are no obvious differences of the burning behaviors between the two fibers.

  18. Development of palm oil-based UV-curable epoxy acrylate and urethane acrylate resins for wood coating application

    NASA Astrophysics Data System (ADS)

    Tajau, Rida; Ibrahim, Mohammad Izzat; Yunus, Nurulhuda Mohd; Mahmood, Mohd Hilmi; Salleh, Mek Zah; Salleh, Nik Ghazali Nik

    2014-02-01

    The trend of using renewable sources such as palm oil as raw material in radiation curing is growing due to the demand from the market to produce a more environmental friendly product. In this study, the radiation curable process was done using epoxy acrylate and urethane acrylate resins which are known as epoxidised palm olein acrylate (EPOLA) and palm oil based urethane acrylate (POBUA), respectively. The purpose of the study was to investigate curing properties and the application of this UV-curable palm oil resins for wood coating. Furthermore, the properties of palm oil based coatings are compared with the petrochemical-based compound such as ebecryl (EB) i.e. EB264 and EB830. From the experiment done, the resins from petrochemical-based compounds resulted higher degree of crosslinking (up to 80%) than the palm oil based compounds (up to 70%), where the different is around 10-15%. The hardness property from this two type coatings can reached until 50% at the lower percentage of the oligomer. However, the coatings from petrochemical-based have a high scratch resistance as it can withstand at least up to 3.0 Newtons (N) compared to the palm oil-based compounds which are difficult to withstand the load up to 1.0 N. Finally, the test on the rubber wood substrate showed that the coatings containing benzophenone photoinitiator give higher adhesion property and their also showed a higher glosiness property on the glass substrate compared to the coatings containing irgacure-819 photoinitiator. This study showed that the palm oil coatings can be a suitable for the replacement of petrochemicals compound for wood coating. The palm oil coatings can be more competitive in the market if the problems of using high percentage palm oil oligomer can be overcome as the palm oil price is cheap enough.

  19. Influence of Zwitterions on Thermomechanical Properties and Morphology of Acrylic Copolymers: Implications for Electroactive Applications

    DTIC Science & Technology

    2011-09-30

    properties of ethyl acrylate and n-butyl acrylate ( nBA )-based sulfobetaine-containing copolymers.10,11 They found that the incorporation of...ammonio]-1-propanesulfonate (SBMA), a zwitterionic mono- mer. Copolymerization of both charge-containing monomers with nBA elucidates the influence of...3-[[2-(methacryloyloxy)ethyl]- (dimethyl)ammonio]-1-propanesulfonate (SBMA), was generously provided by Raschig GmbH. n-Butyl acrylate ( nBA , Alfa

  20. N-Butyl acrylate polymer composition for solar cell encapsulation and method

    NASA Technical Reports Server (NTRS)

    Gupta, Amitava (Inventor); Ingham, John D. (Inventor); Yavrouian, Andre H. (Inventor)

    1983-01-01

    A polymer syrup for encapsulating solar cell assemblies. The syrup includes uncrosslinked poly(n-butyl)acrylate dissolved in n-butyl acrylate monomer. Preparation of the poly(n-butyl)acrylate and preparation of the polymer syrup is disclosed. Methods for applying the polymer syrup to solar cell assemblies as an encapsulating pottant are described. Also included is a method for solar cell construction utilizing the polymer syrup as a dual purpose adhesive and encapsulating material.

  1. Comparison between an Acrylic Splint Herbst and an Acrylic Splint Miniscrew-Herbst for Mandibular Incisors Proclination Control

    PubMed Central

    Manni, Antonio; Pasini, Marco; Nuzzo, Claudio; Grassi, Felice Roberto

    2014-01-01

    Aim. The aim of this study is to compare dental and skeletal effects produced by an acrylic splint Herbst with and without skeletal anchorage for correction of dental class II malocclusion. Methods. The test group was formed by 14 patients that were treated with an acrylic splint miniscrew-Herbst; miniscrews were placed between mandibular second premolars and first molars; controls also consisted of 14 subjects that were treated with an acrylic splint Herbst and no miniscrews. Cephalometric measurements before and after Herbst treatment were compared. The value of α for significance was set at 0.05. Results. All subjects from both groups were successfully treated to a bilateral Class I relationship; mean treatment time was 8,1 months in the test group and 7.8 in the controls. Several variables did not have a statistical significant difference between the two groups. Some of the variables, instead, presented a significant difference such as incisor flaring, mandibular bone base position, and skeletal discrepancy. Conclusions. This study showed that the Herbst appliance associated to miniscrews allowed a better control of the incisor flaring with a greater mandibular skeletal effect. PMID:24963293

  2. Fibrillation of Commercial Acrylic Fiber for Use in Combustible Cartridge Cases

    DTIC Science & Technology

    1983-03-01

    flow chart 3 2 Fiber identification magnified 4 3 80X view acrylic fibers 5 4 320X view acrylic fibers 5 5 80X view kraft 6 6 320X view kraft 6 7 80X...view acrylic, kraft , and nitrocellulose 7 8 80X view after addition of Lufax 295 7 9 80X view 5 minutes after addition of resin 8 10 80X view 10...ACRYLIC KRAFT NITROCELLULOSE (FibrilHated) (Natural) (Natural) Figure 2. Fiber identification magnified Additional views of the fibers in slurry

  3. Anomerization of Acrylated Glucose During Traveling Wave Ion Mobility Spectrometry

    NASA Astrophysics Data System (ADS)

    Chendo, Christophe; Moreira, Guillaume; Tintaru, Aura; Posocco, Paola; Laurini, Erik; Lefay, Catherine; Gigmes, Didier; Viel, Stéphane; Pricl, Sabrina; Charles, Laurence

    2015-09-01

    Anomerization of simple sugars in the liquid phase is known as an acid- and base-catalyzed process, which highly depends on solvent polarity. This reaction is reported here to occur in the gas phase, during traveling wave ion mobility spectrometry (TWIMS) experiments aimed at separating α- and β-anomers of penta-acrylated glucose generated as ammonium adducts in electrospray ionization. This compound was available in two samples prepared from glucose dissolved in solvents of different polarity, namely tetrahydrofuran (THF) and N,N-dimethylacetamide (DMAC), and analyzed by electrospray tandem mass spectrometry (ESI-MS/MS) as well as traveling wave ion mobility (ESI-TWIMS-MS). In MS/MS, an anchimerically-assisted process was found to be unique to the electrosprayed α-anomer, and was only observed for the THF sample. In ESI-TWIMS-MS, a signal was measured at the drift time expected for the α-anomer for both the THF and DMAC samples, in apparent contradiction to the MS/MS results, which indicated that the α-anomer was not present in the DMAC sample. However, MS/MS experiments performed after TWIMS separation revealed that ammonium adducts of the α-anomer produced from each sample, although exhibiting the same collision cross section, were clearly different. Indeed, while the α-anomer actually present in the THF sample was electrosprayed with the ammonium adducted at the C2 acrylate, its homologue only observed when the DMAC sample was subjected to TWIMS hold the adducted ammonium at the C1 acrylate. These findings were explained by a β/α inter-conversion upon injection in the TWIMS cell, as supported by theoretical calculation and dynamic molecular modeling.

  4. Reactivity of Monovinyl (Meth)Acrylates Containing Cyclic Carbonates.

    PubMed

    Berchtold, Kathryn A; Nie, Jun; Stansbury, Jeffrey W; Bowman, Christopher N

    2008-12-09

    The tremendous diversity of materials properties available with polymers is due in large part to the ability to design structures from the monomeric state. The ease of use of comonomer mixtures only expands this versatility. While final polymer properties are obviously important in the selection or development of a material for a given purpose, for a number of applications, such as optical fiber coatings, photolithography and microelectronics, the additional requirement of a very rapid polymerization process may be equally critical. A class of unusually reactive mono-(meth)acrylate monomers bearing secondary functionality that includes carbonates, carbamates and oxazolidones, has been demonstrated but not fully explained. Here, the influence of an integral cyclic carbonate functional group on (meth)acrylate photopolymerization kinetics is examined in detail with respect to monomers with a wide variety of alternative secondary functionality structure as well as in comparison to conventional mono- and di-(meth)acrylates. The kinetic results from full cure studies of several cyclic carbonate-containing monomers clearly highlight specific structural variations that effectively promote monomer reactivity. Copolymerizations with tetrahydrofurfuryl methacrylate reflect similar dramatic kinetic effects associated with the novel monomers while partial cure homopolymerization studies reveal exceptional dark cure behavior linked to observations of uncommonly low ratios of termination to propagation rates throughout the conversion profile. Temperature effects on reaction kinetics, including both reaction rate and the individual kinetic parameters, as well as the temperature dependence of hydrogen bonding interactions specifically involving the secondary functional groups are probed as a means to understand better the fundamentally interesting and practically important behavior of these monomers.

  5. Depositing highly adhesive optical thin films on acrylic substrates.

    PubMed

    Takahashi, Tomoaki; Harada, Toshinori; Murotani, Hiroshi; Matumoto, Shigeharu

    2014-02-01

    Optical thin films are used to control the reflectance and transmittance of optical components. However, conventional deposition technologies applicable to organic (plastic) substrates typically result in weak adhesion. We overcame this problem by using vacuum deposition in combination with sputtering to directly deposit a SiO2 optical thin film onto an acrylic resin substrate. We observed neither yellowing nor deformation. The hardness of the film is 2H as measured by the pencil hardness test, indicating successful modulation of optical properties without sacrificing substrate hardness.

  6. Dimensional accuracy and stability of acrylic resin denture bases.

    PubMed

    Huggett, R; Zissis, A; Harrison, A; Dennis, A

    1992-10-01

    Proponents of injection molding systems have claimed a number of benefits over conventional press-pack dough molding systems. The aim of this study was to evaluate a recently developed injection (dry heat) procedure of processing compared with press-pack dough molding utilizing three curing cycles. The dimensional accuracy and stability of acrylic resin bases produced by the two molding procedures were compared. Dimensional changes were assessed over a period of 4 months using an optical comparator. The results demonstrate that baseplates produced by the injection molding procedure exhibit less shrinkage than those produced by the conventional press-pack procedures.

  7. Acrylic Plastic Spherical Pressure Hull for Continental Shelf Depths

    DTIC Science & Technology

    1993-03-01

    depth reached so far by acrylic plas - appears to meet the design depth requirement for tic submersibles is 3,300 feet (1,000 meters). Still, 8,000 feet...temperature, and time. than 0.05 tend to fail primarily by general, or local, elastic instability, and for ",$-is reason, the design 3. The rate of strain...loading to t/DO membrane compressive strain exceeds a cer- ratio at ambient room temperature. tain threshold value. Elastic , plastic, and creep

  8. Synthesis and characterization of acrylic-based superabsorbents

    SciTech Connect

    Askari, F.; Nafisi, S.; Omidian, H.; Hashemi, S.A. )

    1993-12-10

    This paper is devoted to the synthesis and characterization of superabsorbent polymers based on acrylic acid. These hydrogels were prepared by carrying the inverse suspension polymerization in an aromatic hydrocarbon. The dispersion is stabilized by the mixture of micromolecular and macromolecular emulsifiers. To obtain high swelling and appropriate absorption kinetics, parameters such as initial monomer and cross-linker concentration, range of neutralization, monomer addition rate, temperature, initiating system, stabilizing system and nature of the organic phase were studied but not reviewed here. Thus, based on these topics a basic formula is obtained to display the effect of some structural parameters on behavior of superabsorbents utilized.

  9. Softec HD hydrophilic acrylic intraocular lens: biocompatibility and precision.

    PubMed

    Espandar, Ladan; Sikder, Shameema; Moshirfar, Majid

    2011-01-10

    Intraocular lens development is driven by higher patient expectations for ideal visual outcomes. The recently US Food and Drug Administration-approved Softec HD(™) lens is an aspheric, hydrophilic acrylic intraocular lens (IOL). The hydrophilic design of the lens is optimized to address dysphotopsia while maintaining biocompatibility, optical clarity, resistance to damage, and resistance to biocontamination. Aspheric lenses decrease postoperative spherical aberration. The addition of the Softec lens provides clinicians with another option for IOL placement; however, randomized comparative studies of this lens to others already on the market remain to be completed.

  10. Softec HD hydrophilic acrylic intraocular lens: biocompatibility and precision

    PubMed Central

    Espandar, Ladan; Sikder, Shameema; Moshirfar, Majid

    2011-01-01

    Intraocular lens development is driven by higher patient expectations for ideal visual outcomes. The recently US Food and Drug Administration-approved Softec HD™ lens is an aspheric, hydrophilic acrylic intraocular lens (IOL). The hydrophilic design of the lens is optimized to address dysphotopsia while maintaining biocompatibility, optical clarity, resistance to damage, and resistance to biocontamination. Aspheric lenses decrease postoperative spherical aberration. The addition of the Softec lens provides clinicians with another option for IOL placement; however, randomized comparative studies of this lens to others already on the market remain to be completed. PMID:21311658

  11. Development of Electrically Conductive Transparent Coatings for Acrylic Plastic

    DTIC Science & Technology

    1952-12-01

    and methyl methacrylate monomer (I mole) in cyciohexanone (Z moles) vw’th benzoyl peroxide catalyst (0, Z% of total weight). The mix- ture was refluxed... methacrylic acid- methyl methaerylate copolymer re•I. The composite material, i. e., the acrylic and applied coating, retains essentially all the original...0.001" to 0.002" when rolled on and of less than 0.001" when sprayed on. The ability of the methacrylic acid- methyl methacrylate copolymer to cover the

  12. Control of contamination of radon-daughters in the DEAP-3600 acrylic vessel

    SciTech Connect

    Jillings, Chris; Collaboration: DEAP Collaboration; and others

    2013-08-08

    DEAP-3600 is a 3600kg single-phase liquid-argon dark matter detector under construction at SNOLAB with a sensitivity of 10{sup −46}cm{sup 2} for a 100 GeV WIMP. The argon is held an an acrylic vessel coated with wavelength-shifting 1,1,4,4-tetraphenyl-1,3-butadiene (TPB). Acrylic was chosen because it is optically transparent at the shifted wavelength of 420 nm; an effective neutron shield; and physically strong. With perfect cleaning of the acrylic surface before data taking the irreducible background is that from bulk {sup 210}Pb activity that is near the surface. To achieve a background rate of 0.01 events in the 1000-kg fiducial volume per year of exposure, the allowed limit of Pb-210 in the bulk acrylic is 31 mBq/tonne (= 1.2 × 10{sup −20}g/g). We discuss how pure acrylic was procured and manufactured into a complete vessel paying particular attention to exposure to radon during all processes. In particular field work at the acrylic panel manufacturer, RPT Asia, and acrylic monomer supplier, Thai MMA Co. Ltd, in Thailand is described. The increased diffusion of radon during annealing the acrylic at 90C as well as techniques to mitigate against this are described.

  13. 40 CFR 721.10530 - Acrylate manufacture byproduct distillation residue (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... distillation residue (generic). 721.10530 Section 721.10530 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10530 Acrylate manufacture byproduct distillation... substance is identified generically as acrylate manufacture byproduct distillation residue (PMN P-12-87)...

  14. 40 CFR 721.10530 - Acrylate manufacture byproduct distillation residue (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... distillation residue (generic). 721.10530 Section 721.10530 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10530 Acrylate manufacture byproduct distillation... substance is identified generically as acrylate manufacture byproduct distillation residue (PMN P-12-87)...

  15. Properties of Ultra-Violet Cured Poly(diemthylsiloxane)-Urea Acrylates.

    DTIC Science & Technology

    1984-11-01

    polycaprolactone) and polyol molecular weight on physical properties were evaluated. TDI/ hydroxyethyl methacrylate ( HEMA ) based samples were also...diluents. The reactive diluents or crosslinkers I. chosen were: ethyl methacrylate (EMA), hydroxyethyl methacrylate ( HEMA ), butyl acrylate (BA...butylacrylate (BA), acrylic acid (AA), ethyl methacrylate (EMA), B- hydroxyethyl ’metthacrylate ( HEMA ), m~ethyl trethacrylate (MMA), and 4-vinylpyridine (4

  16. Synthesis of Radiation Curable Palm Oil-Based Epoxy Acrylate: NMR and FTIR Spectroscopic Investigations.

    PubMed

    Salih, Ashraf M; Ahmad, Mansor Bin; Ibrahim, Nor Azowa; Dahlan, Khairul Zaman Hj Mohd; Tajau, Rida; Mahmood, Mohd Hilmi; Yunus, Wan Md Zin Wan

    2015-08-04

    Over the past few decades, there has been an increasing demand for bio-based polymers and resins in industrial applications, due to their potential lower cost and environmental impact compared with petroleum-based counterparts. The present research concerns the synthesis of epoxidized palm oil acrylate (EPOLA) from an epoxidized palm oil product (EPOP) as environmentally friendly material. EPOP was acrylated by acrylic acid via a ring opening reaction. The kinetics of the acrylation reaction were monitored throughout the reaction course and the acid value of the reaction mixture reached 10 mg KOH/g after 16 h, indicating the consumption of the acrylic acid. The obtained epoxy acrylate was investigated intensively by means of FTIR and NMR spectroscopy, and the results revealed that the ring opening reaction was completed successfully with an acrylation yield about 82%. The UV free radical polymerization of EPOLA was carried out using two types of photoinitiators. The radiation curing behavior was determined by following the conversion of the acrylate groups. The cross-linking density and the hardness of the cured EPOLA films were measured to evaluate the effect of the photoinitiator on the solid film characteristics, besides, the thermal and mechanical properties were also evaluated.

  17. Preparation and properties of acrylic resin coating modified by functional graphene oxide

    NASA Astrophysics Data System (ADS)

    Dong, Rui; Liu, Lili

    2016-04-01

    To improve the dispersion and the strength of filler-matrix interface in acrylic resin, the functional graphene oxide (FGO) was obtained by surface modification of graphene oxide (GO) by γ-methacryloxypropyl trimethoxysilane (KH-570) and then the acrylic nanocomposites containing different loadings of GO and FGO were prepared. The structure, morphology and dispersion/exfoliation of the FGO were characterized by XRD, FT-IR, Raman, XPS, SEM and TEM. The results demonstrated that the KH-570 was successfully grafted onto the surface of GO sheets. Furthermore, the corresponding thermal, mechanical and chemical resistance properties of the acrylic nanocomposites filled with the FGO were studied and compared with those of neat acrylic and GO/acrylic nanocomposites. The results revealed that the loading of FGO effectively enhanced various properties of acrylic resin. These findings confirmed that the dispersion and interfacial interaction were greatly improved by incorporation of FGO, which might be the result of covalent bonds between the FGO and the acrylic matrix. This work demonstrates an in situ polymerization method to construct a flexible interphase structure, strong interfacial interaction and good dispersion of FGO in acrylic nanocomposites, which can reinforce the polymer properties and be applied in research and industrial areas.

  18. The acute aquatic toxicity of a series of acrylate and methacrylate esters

    SciTech Connect

    Staples, C.A.; McLaughlin, J.E.; Hamilton, J.D.

    1994-12-31

    Acute aquatic toxicity data for several acrylate and methacrylate esters were reviewed. Acrylates included acrylic acid, ethyl-, and butyl-acrylate. Methacrylates included methacrylic acid, methyl-, and butyl-methacrylate. Tests were 48 hr or 96 hr standard flow through (invertebrates and fish) assays (measured exposure concentrations). These data are currently used in a risk assessment of acrylate/methacrylate environmental safety. Algal growth (Selanastrum capricomutum) 96 hr EC{sub 50}s were 0.17 mg/L (NOEC < 0.13 mg/L) for acrylic acid, 11.0 mg/L (NOEC < 6.5 mg/L) for ethyl acrylate, and 5.2 mg/L (NOEC < 3.8 mg/L) for butyl acrylate. Invertebrate (Daphnia magna) 48 hr LC{sub 50}s were 95.0 mg/L (NOEC 23.0 mg/L) for acrylic acid, 7.9 mg/L (NOEC 3.4 mg/L) for ethyl acrylate, and 8.2 mg/L (NOEC 2.4 mg/L) for butyl acrylate. Rainbow trout (Oncorhynchus mykiss) 96 hr LC{sub 50}s were 27.0 mg/L (NOEC 6.3 mg/L) for acrylic acid, 4.6 mg/L (NOEC 0.78 mg/L) for ethyl acrylate, and 5.2 mg/L (NOEC 3.8 mg/L) for butyl acrylate. Algae 96 hr EC{sub 50}s were 0.59 mg/L (NOEC 0.38 mg/L) for methacrylic acid, 170.0 mg/L (NOEC 100.0 mg/L) for methyl methacrylate, and 130.0 mg/L for butyl methacrylate. Daphnia magna 48 hr LC{sub 50}s were > 130.0 mg/L (NOEC 130.0 mg/L) for methacrylic acid, 69.0 mg/L (NOEC 48.0 mg/L) for methyl methacrylate, and 32.0 mg/L (NOEC 23.0 mg/L) for butyl methacrylate. Trout 96 hr LC{sub 50}s were 85.0 mg/L (NOEC 12.0 mg/L) for methacrylic acid and > 79.0 mg/L (NOEC 40.0 mg/L) for methyl methacrylate. The fathead minnow (Pimephales promelas) 96 hr LC{sub 50} was 11.0 mg/L for butyl methacrylate.

  19. Influence of Sea Water Aging on the Mechanical Behaviour of Acrylic Matrix Composites

    NASA Astrophysics Data System (ADS)

    Davies, P.; Le Gac, P.-Y.; Le Gall, M.

    2016-07-01

    A new matrix resin was recently introduced for composite materials, based on acrylic resin chemistry allowing standard room temperature infusion techniques to be used to produce recyclable thermoplastic composites. This is a significant advance, particularly for more environmentally-friendly production of large marine structures such as boats. However, for such applications it is essential to demonstrate that composites produced with these resins resist sea water exposure in service. This paper presents results from a wet aging study of unreinforced acrylic and glass and carbon fibre reinforced acrylic composites. It is shown that the acrylic matrix resin is very stable in seawater, showing lower property losses after seawater aging than those of a commonly-used epoxy matrix resin. Carbon fibre reinforced acrylic also shows good property retention after aging, while reductions in glass fibre reinforced composite strengths suggest that specific glass fibre sizing may be required for optimum durability.

  20. The study of synthesis and photocuring behaviors of organic silicon modified methylacrylate and acrylate

    NASA Astrophysics Data System (ADS)

    Wang, Si-yuan; Zou, Ying-quan

    2012-03-01

    Ten different silicon-containing methyl acrylate and acrylate monomers were synthesized by the substitution reaction of chlorosilanes or chlorosiloxanes with 2-Hydroxyethyl methacrylate or 2-Hydroxyethyl acrylate. Using triethylamine as the catalytic agent, tetrahydrofuran as the solvent, pure products can be obtained with one-step reaction after reduced pressure distillation or column chromatography via controlling raw ratio and reaction time. In this study, one to four silicon contained methyl acrylate and acrylate monomers were synthesized with simple methd and high yield. Monomers' properties were characterized through IR, 1H-NMR, 13C-NMR and their viscosity and thermostability were also characterized. The polymers' have good performance on UV-curing and low surface energy.

  1. Biocatalytic synthesis of maltodextrin-based acrylates from starch and α-cyclodextrin.

    PubMed

    Kloosterman, Wouter M J; Spoelstra-van Dijk, Gerda; Loos, Katja

    2014-09-01

    Novel 2-(β-maltooligooxy)-ethyl (meth)acrylate monomers are successfully synthesized by CGTase from Bacillus macerans catalyzed coupling of 2-(β-glucosyloxy)-ethyl acrylate and methacrylate with α-cyclodextrin or starch. HPLC-UV analysis shows that the CGTase catalyzed reaction yields 2-(β-maltooligooxy)-ethyl acrylates with 1 to 15 glucopyranosyl units. (1) H NMR spectroscopy reveals that the β-linkage in the acceptor molecule is preserved during the CGTase catalyzed coupling reaction, whereas the newly introduced glucose units are attached by α-(1,4)-glycosidic linkages. The synthesized 2-(β-maltooligooxy)-ethyl acrylate monomers are successfully polymerized by aqueous free radical polymerization to yield the comb-shaped glycopolymer poly(2-(β-maltooligooxy)-ethyl acrylate).

  2. Influence of Sea Water Aging on the Mechanical Behaviour of Acrylic Matrix Composites

    NASA Astrophysics Data System (ADS)

    Davies, P.; Le Gac, P.-Y.; Le Gall, M.

    2017-02-01

    A new matrix resin was recently introduced for composite materials, based on acrylic resin chemistry allowing standard room temperature infusion techniques to be used to produce recyclable thermoplastic composites. This is a significant advance, particularly for more environmentally-friendly production of large marine structures such as boats. However, for such applications it is essential to demonstrate that composites produced with these resins resist sea water exposure in service. This paper presents results from a wet aging study of unreinforced acrylic and glass and carbon fibre reinforced acrylic composites. It is shown that the acrylic matrix resin is very stable in seawater, showing lower property losses after seawater aging than those of a commonly-used epoxy matrix resin. Carbon fibre reinforced acrylic also shows good property retention after aging, while reductions in glass fibre reinforced composite strengths suggest that specific glass fibre sizing may be required for optimum durability.

  3. Characteristics and mechanisms of acrylate polymer damage to maize seedlings.

    PubMed

    Chen, Xian; Mao, Xiaoyun; Lu, Qin; Liao, Zongwen; He, Zhenli

    2016-07-01

    Superabsorbent acrylate polymers (SAPs) have been widely used to maintain soil moisture in agricultural management, but they may cause damage to plants, and the mechanisms are not well understood. In this study, seed germination, soil pot culture, hydroponic experiments, and SAPs degradation were conducted to investigate damage characteristics and mechanisms associated with SAPs application. The Results showed that SAPs inhibited maize growth and altered root morphology (irregular and loose arrangement of cells and breakage of cortex parenchyma), and the inhibitory effects were enhanced at higher SAPs rates. After 1h SAP hydrogels treatment, root malondialdehyde (MDA) content was significantly increased, while superoxide dismutase (SOD) and catalase (CAT) content were significantly decreased. Hydroponics experiment indicated that root and shoot growth was inhibited at 2.5mgL(-1) acrylic acid (AA), and the inhibition was enhanced with increasing AA rates. This effect was exacerbated by the presence of Na(+) at a high concentration in the hydrogels. Release and degradation of AA were enhanced at higher soil moisture levels. A complete degradation of AA occurred between 15 and 20 days after incubation (DAI), but it took longer for Na(+) concentration to decrease to a safe level. These results indicate that high concentration of both AA and Na(+) present in the SAPs inhibits plant growth. The finding of this study may provide a guideline for appropriate application of SAPs in agriculture.

  4. Dissociative photoionization of ethyl acrylate: Theoretical and experimental insights

    NASA Astrophysics Data System (ADS)

    Song, Yanlin; Chen, Jun; Ding, Mengmeng; Wei, Bin; Cao, Maoqi; Shan, Xiaobin; Zhao, Yujie; Huang, Chaoqun; Sheng, Liusi; Liu, Fuyi

    2015-08-01

    The photoionization and dissociation of ethyl acrylate have been investigated by time-of-flight mass spectrometer with tunable vacuum ultraviolet (VUV) source in the range of 9.0-20.0 eV. The photoionization mass spectrum (PIMS) for ethyl acrylate and photoionization efficiency (PIE) curves for its major fragment ions: C5H7O2+, C4H5O2+, C3H5O2+, C3H4O+, C3H3O+, C2H5O+, C2H3O+, C2H5+ and C2H4+ have been obtained. The formation channels of main fragments are predicted by Gaussian 09 program at G3B3 level and examined via their dissociation energies from experimental results. Based on our analysis, nine main dissociative photoionization channels are proposed: C5H7O2+ + H, C4H5O2+ + CH3, C3H5O2+ + C2H3, C3H4O+ + C2H4O, C3H3O+ + C2H5O, C2H5O+ + C3H3O, C2H3O+ + C3H5O, C2H5+ + C3H3O2, C2H4+ + C3H4O2, respectively. The results of this work lead to a better understanding of photochemistry in the environment.

  5. Dissipation factor of acrylic dielectric elastomer--an experimental study.

    PubMed

    Sahu, Raj Kumar; Pramanik, Bipul; Patra, Karali; Bhaumik, Shovan; Pandey, Arvind Kumar; Setua, Dipak Kumar

    2014-10-01

    This paper studies the effects of frequency, pre-strain and electrode types on the dielectric property of a commercially available and most widely used acrylic elastomer, VHB 4910. The acrylic VHB film is pre-stretched in biaxial directions with the help of an in-house developed biaxial stretching device. The stretched film has been sandwiched between two card board frames to prepare samples of different pre-stretch values. Three different types of electrodes namely copper tape, silver grease and carbon grease have been pasted on the both sides of prestretched samples. Dissipation factor of pre-stretched and electrode adhered VHB sample has been experimentally determined at different frequency (upto 1 MHz) of input voltage using a LCR meter. Experimental results on the variation of dissipation factor with pre-straining, frequency (low to high) and electrode types are reported. The dissipation factor value is further used to estimate electrical efficiency at different biaxial pre-straining, frequency and electrode types.

  6. Color difference threshold determination for acrylic denture base resins.

    PubMed

    Ren, Jiabao; Lin, Hong; Huang, Qingmei; Liang, Qifan; Zheng, Gang

    2015-01-01

    This study aimed to set evaluation indicators, i.e., perceptibility and acceptability color difference thresholds, of color stability for acrylic denture base resins for a spectrophotometric assessing method, which offered an alternative to the visual method described in ISO 20795-1:2013. A total of 291 disk specimens 50±1 mm in diameter and 0.5±0.1 mm thick were prepared (ISO 20795-1:2013) and processed through radiation tests in an accelerated aging chamber (ISO 7491:2000) for increasing times of 0 to 42 hours. Color alterations were measured with a spectrophotometer and evaluated using the CIE L*a*b* colorimetric system. Color differences were calculated through the CIEDE2000 color difference formula. Thirty-two dental professionals without color vision deficiencies completed perceptibility and acceptability assessments under controlled conditions in vitro. An S-curve fitting procedure was used to analyze the 50:50% perceptibility and acceptability thresholds. Furthermore, perceptibility and acceptability against the differences of the three color attributes, lightness, chroma, and hue, were also investigated. According to the S-curve fitting procedure, the 50:50% perceptibility threshold was 1.71ΔE00 (r(2)=0.88) and the 50:50% acceptability threshold was 4.00 ΔE00 (r(2)=0.89). Within the limitations of this study, 1.71/4.00 ΔE00 could be used as perceptibility/acceptability thresholds for acrylic denture base resins.

  7. Wet air oxidation of epoxy acrylate monomer industrial wastewater.

    PubMed

    Yang, Shaoxia; Liu, Zhengqian; Huang, Xiaohui; Zhang, Beiping

    2010-06-15

    Epoxy acrylate monomer industrial wastewater contained highly concentrated and toxic organic compounds. The wet air oxidation (WAO) and catalytic wet air oxidation (CWAO) were used to eliminate pollutants in order to examine the feasibility of the WAO/CWAO as a pre-treatment method for the industrial wastewater. The results showed that in the WAO 63% chemical oxygen demand (COD) and 41% total organic carbon (TOC) removals were achieved and biological oxygen demand (BOD(5))/COD ratio increased from 0.13 to 0.72 after 3h reaction at 250 degrees C, 3.5MPa and the initial concentration of 100g(COD)/L. Among homogenous catalysts (Cu(2+), Fe(2+), Fe(3+) and Mn(2+) salts), Cu(2+) salt exhibited better performance. CuO catalyst was used in the CWAO of the wastewater, COD and TOC conversion were 77 and 54%, and good biodegradability was achieved. The results proved that the CWAO was an effective pre-treatment method for the epoxy acrylate monomer industrial wastewater.

  8. Acrylic Resin Molding Based Head Fixation Technique in Rodents.

    PubMed

    Roh, Mootaek; Lee, Kyungmin; Jang, Il-Sung; Suk, Kyoungho; Lee, Maan-Gee

    2016-01-12

    Head fixation is a technique of immobilizing animal's head by attaching a head-post on the skull for rigid clamping. Traditional head fixation requires surgical attachment of metallic frames on the skull. The attached frames are then clamped to a stationary platform resulting in immobilization of the head. However, metallic frames for head fixation have been technically difficult to design and implement in general laboratory environment. In this study, we provide a novel head fixation method. Using a custom-made head fixation bar, head mounter is constructed during implantation surgery. After the application of acrylic resin for affixing implants such as electrodes and cannula on the skull, additional resins applied on top of that to build a mold matching to the port of the fixation bar. The molded head mounter serves as a guide rails, investigators conveniently fixate the animal's head by inserting the head mounter into the port of the fixation bar. This method could be easily applicable if implantation surgery using dental acrylics is necessary and might be useful for laboratories that cannot easily fabricate CNC machined metal head-posts.

  9. Graft copolymerization of acrylic acid onto polyamide fibers

    NASA Astrophysics Data System (ADS)

    Makhlouf, Chahira; Marais, Stéphane; Roudesli, Sadok

    2007-04-01

    The grafting of acrylic acid (AA) monomer (CH 2dbnd CH sbnd COOH) on polyamide 6.6 monofilaments (PA 6.6) using benzoyl peroxide (BPO) as initiator was carried out in order to enhance the hydrophilic nature of fibers. The grafting rate depends on the AA concentration, the BPO concentration, the time and the temperature of reaction. The best conditions for optimum rate of grafting were obtained with a AA concentration of 0.5 M, a BPO concentration of 0.03 M, a reaction temperature of T = 85 °C and a reaction time of 120 mn. The fiber surface has been investigated by many experimental techniques of characterization such as Fourier transform infrared spectroscopy (FTIR), calorimetric analysis (DSC), scanning electron microscopy (SEM), and contact angle measurements. The effect of grafting of acrylic acid onto PA 6.6 fibers on their moisture and mechanical resistances was analyzed from water sorption and elongation at break measurements. The analysis of the experimental data shows clearly the efficiency of the grafting reaction used, leading to a significant increase of the hydrophilic character of the PA 6.6 surface.

  10. In vitro measurement of bone-acrylic interface pressure during femoral component insertion.

    PubMed

    Markolf, K L; Amstutz, H C

    1976-01-01

    Bone-acrylic interface pressure measurements were recorded at the medial interior rasped surfaces of fresh cadaver femurs during digital packing of acrylic bone cement and during insertion and seating of a Trapezoidal-28 femoral total hip component. Plugging of the femoral canal below the tip of the prosthesis stem was an effective means for increasing pressure in the distal femoral canal when the stem was inserted in the early stages of acrylic polymerization (i.e. immediately after dough time). At surgery, this can be accomplished by inserting a small bolus of acrylic down the canal to a depth below the tip of the seated stem and allowing it to polymerize in place. This forms an effective seal which prevents distal extrusion of the acrylic when the cavity is then packed prior to prosthesis insertion. Elimination of cement in the distal canal also avoids any future difficulty of acrylic removal should revision become necessary due to loosening or infection. No significant pressure differences were observed between one and two millimeter thicknesses of acrylic between the metal and bone. Interface pressures developed during finger packing were of the same order of magnitude as those achieved during seating of the femoral component. Use of a rubber diaphragm stretched tightly over the margins of the rasped femoral cavity helped to contain the acrylic and prevent extrusion during finger packing but was ineffective in increasing interface pressure. When this method is used, the acrylic can be poured or injected into the canal and packed before dough stage and thus facilitate increased cancellous penetration when the acrylic is in a state of low viscosity.

  11. Facile Fabrication of Gradient Surface Based on (meth)acrylate Copolymer Films

    NASA Astrophysics Data System (ADS)

    Zhang, Y.; Yang, H.; Wen, X.-F.; Cheng, J.; Xiong, J.

    2016-08-01

    This paper describes a simple and economic approach for fabrication of surface wettability gradient on poly(butyl acrylate - methyl methacrylate) [P (BA-MMA)] and poly(butyl acrylate - methyl methacrylate - 2-hydroxyethyl methacrylate) [P (BA-MMA-HEMA)] films. The (meth)acrylate copolymer [including P (BA-MMA) and P (BA-MMA-HEMA)] films are hydrolyzed in an aqueous solution of NaOH and the transformation of surface chemical composition is achieved by hydrolysis in NaOH solution. The gradient wetting properties are generated based on different functional groups on the P (BA-MMA) and P (BA-MMA-HEMA) films. The effects of both the surface chemical and surface topography on wetting of the (meth)acrylate copolymer film are discussed. Surface chemical composition along the materials length is determined by XPS, and surface topography properties of the obtained gradient surfaces are analyzed by FESEM and AFM. Water contact angle system (WCAs) results show that the P (BA-MMA-HEMA) films provide a larger slope of the gradient wetting than P (BA-MMA). Moreover, this work demonstrates that the gradient concentration of chemical composition on the poly(meth) acrylate films is owing to the hydrolysis processes of ester group, and the hydrolysis reactions that have negligible influence on the surface morphology of the poly(meth) acrylate films coated on the glass slide. The gradient wettability surfaces may find broad applications in the field of polymer coating due to the compatibility of (meth) acrylate polymer.

  12. Gel polymer electrolytes based on nanofibrous polyacrylonitrile–acrylate for lithium batteries

    SciTech Connect

    Kim, Dul-Sun; Woo, Jang Chang; Youk, Ji Ho; Manuel, James; Ahn, Jou-Hyeon

    2014-10-15

    Graphical abstract: - Highlights: • Nanofibrous polyacrylonitrile–acrylate membranes were prepared by electrospinning. • Trimethylolpropane triacrylate was used as a crosslinking agent of fibers. • The GPE based on PAN–acrylate (1/0.5) showed good electrochemical properties. - Abstract: Nanofibrous membranes for gel polymer electrolytes (GPEs) were prepared by electrospinning a mixture of polyacrylonitrile (PAN) and trimethylolpropane triacrylate (TMPTA) at weight ratios of 1/0.5 and 1/1. TMPTA is used to achieve crosslinking of fibers thereby improving mechanical strength. The average fiber diameters increased with increasing TMPTA concentration and the mechanical strength was also improved due to the enhanced crosslinking of fibers. GPEs based on electrospun membranes were prepared by soaking them in a liquid electrolyte of 1 M LiPF{sub 6} in ethylene carbonate (EC)/dimethyl carbonate (DMC) (1:1, v/v). The electrolyte uptake and ionic conductivity of GPEs based on PAN and PAN–acrylate (weight ratio; 1/1 and 1/0.5) were investigated. Ionic conductivity of GPEs based on PAN–acrylate was the highest for PAN/acrylate (1/0.5) due to the proper swelling of fibers and good affinity with liquid electrolyte. Both GPEs based on PAN and PAN–acrylate membranes show good oxidation stability, >5.0 V vs. Li/Li{sup +}. Cells with GPEs based on PAN–acrylate (1/0.5) showed remarkable cycle performance with high initial discharge capacity and low capacity fading.

  13. The photocatalytic enhancement of acrylic and PET solar water disinfection (SODIS) bottles.

    PubMed

    Carey, J M; Perez, T M; Arsiaga, E G; Loetscher, L H; Boyd, J E

    2011-01-01

    The solar water disinfection method (SODIS) was modified by the addition of a photocatalytic layer of titania on the interior surface of polyethylene terephthalate (PET) and acrylic bottles. Titania was solvent deposited on the interior of commercially available PET bottles, as well as bottles that were constructed from acrylic. Uncoated and titania-coated acrylic bottles removed 3,000,000-5,000,000 colony forming units per milliliter of K12 E. coli from 670 mL of contaminated water in 40 min of solar irradiance. After five hours of sunlight exposure, the concentration of 10 ppm methyl orange (a representative organic water contaminant), was reduced by 61% using the titania-coated acrylic bottles. The concentration of 87 ppb microcystin-LR (a representative algal toxin) was reduced by 70% after 7 hours of sunlight exposure in the titania-coated acrylic bottles. Acrylic is an effective alternative to PET for use in the SODIS method due to its greater UV transparency. The addition of titania to PET and acrylic bottles confers the ability to remove chemical contaminants in addition to inactivating microbiological contaminants.

  14. An ORMOSIL-Containing Orthodontic Acrylic Resin with Concomitant Improvements in Antimicrobial and Fracture Toughness Properties

    PubMed Central

    Rueggeberg, Frederick A.; Niu, Li-na; Mettenberg, Donald; Yiu, Cynthia K. Y.; Blizzard, John D.; Wu, Christine D.; Mao, Jing; Drisko, Connie L.; Pashley, David H.; Tay, Franklin R.

    2012-01-01

    Global increase in patients seeking orthodontic treatment creates a demand for the use of acrylic resins in removable appliances and retainers. Orthodontic removable appliance wearers have a higher risk of oral infections that are caused by the formation of bacterial and fungal biofilms on the appliance surface. Here, we present the synthetic route for an antibacterial and antifungal organically-modified silicate (ORMOSIL) that has multiple methacryloloxy functionalities attached to a siloxane backbone (quaternary ammonium methacryloxy silicate, or QAMS). By dissolving the water-insoluble, rubbery ORMOSIL in methyl methacrylate, QAMS may be copolymerized with polymethyl methacrylate, and covalently incorporated in the pressure-processed acrylic resin. The latter demonstrated a predominantly contact-killing effect on Streptococcus mutans ATCC 36558 and Actinomyces naselundii ATCC 12104 biofilms, while inhibiting adhesion of Candida albicans ATCC 90028 on the acrylic surface. Apart from its favorable antimicrobial activities, QAMS-containing acrylic resins exhibited decreased water wettability and improved toughness, without adversely affecting the flexural strength and modulus, water sorption and solubility, when compared with QAMS-free acrylic resin. The covalently bound, antimicrobial orthodontic acrylic resin with improved toughness represents advancement over other experimental antimicrobial acrylic resin formulations, in its potential to simultaneously prevent oral infections during appliance wear, and improve the fracture resistance of those appliances. PMID:22870322

  15. Antimicrobial activity of a quaternary ammonium methacryloxy silicate-containing acrylic resin: a randomised clinical trial

    PubMed Central

    Liu, Si-ying; Tonggu, Lige; Niu, Li-na; Gong, Shi-qiang; Fan, Bing; Wang, Liguo; Zhao, Ji-hong; Huang, Cui; Pashley, David H.; Tay, Franklin R.

    2016-01-01

    Quaternary ammonium methacryloxy silicate (QAMS)-containing acrylic resin demonstrated contact-killing antimicrobial ability in vitro after three months of water storage. The objective of the present double-blind randomised clinical trial was to determine the in vivo antimicrobial efficacy of QAMS-containing orthodontic acrylic by using custom-made removable retainers that were worn intraorally by 32 human subjects to create 48-hour multi-species plaque biofilms, using a split-mouth study design. Two control QAMS-free acrylic disks were inserted into the wells on one side of an orthodontic retainer, and two experimental QAMS-containing acrylic disks were inserted into the wells on the other side of the same retainer. After 48 hours, the disks were retrieved and examined for microbial vitality using confocal laser scanning microscopy. No harm to the oral mucosa or systemic health occurred. In the absence of carry-across effect and allocation bias (disks inserted in the left or right side of retainer), significant difference was identified between the percentage kill in the biovolume of QAMS-free control disks (3.73 ± 2.11%) and QAMS-containing experimental disks (33.94 ± 23.88%) retrieved from the subjects (P ≤ 0.001). The results validated that the QAMS-containing acrylic exhibits favourable antimicrobial activity against plaque biofilms in vivo. The QAMS-containing acrylic may also be used for fabricating removable acrylic dentures. PMID:26903314

  16. Anomalous χ for Polydisperse Polystyrene-b-Poly(octyl acrylate)

    NASA Astrophysics Data System (ADS)

    Lee, Jumi; Ahn, Hyungju; Ryu, Du Yeol; Shin, Kwanwoo; Cho, Junhan

    2012-02-01

    We have performed small-angle neutron scattering (SANS) measurements on a disordered block copolymer from deuterated polystyrene (dPS) and self-adhesive poly(octyl acrylate) (POA) in order to elicit the effective Flory-Huggins χ, which carries the essence of the copolymer phase behavior. The sample for the measurement was prepared by blending two polydisperse dPS-b-POAs of different molecular weights for the purpose of adjusting the average size to a proper value. The SANS profiles for the copolymer were fitted to Leibler's scattering function for a polydisperse copolymer system described by Schulz-Zimm distribution. It was shown that the resultant χ as a function of inverse temperature has a strong entropic contribution and a weak enthalpic contribution. By adopting a simple analysis for specific interactions, it was found that the entropically dominated χ for dPS-b-POA arises from the steric hindrance of long alkyl side groups of POA.

  17. Photoinduced Acrylate Polymerization: Unexpected Reduction in Chain Branching.

    PubMed

    Wenn, Benjamin; Reekmans, Gunter; Adriaensens, Peter; Junkers, Thomas

    2015-08-01

    The branching stemming from midchain radical formation in n-butyl acrylate polymerization is investigated via melt-state (13) C NMR measurements. The dependence of the degree of branching (DB) on the monomer conversion of the system is examined for photoinduced polymerizations, revealing a steady increase in branching with conversion. For polymerization at moderate light intensities, an increase in branching from 0.03% to 0.37% is observed for polymerizations at 60 °C, which is fivefold below the level of branching observed in thermally initiated polymerizations under otherwise identical reaction conditions. The reason for this overall reduction in branching remains momentarily unclear; yet, a strong dependence of branching on light intensity is observed. While polymerization under a 1 W LED lamp results at almost full monomer conversion in branching degrees of 0.22%, polymerization under a 400 W lamp yields 1.81% of chain branches.

  18. Laboratory analyses of two explanted hydrophobic acrylic intraocular lenses.

    PubMed

    Dai, Yunhai; Huang, Yusen; Liu, Ting; Xie, Lixin

    2014-06-01

    Two three-piece hydrophobic acrylic intraocular lenses (IOLs) were explanted from two patients at 7 and 9 years, respectively, after implantation, because of poor fundus visualisation and/or a clinically significant decrease in visual acuity related to their opacified IOLs. In addition to light microscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy, confocal laser scanning microscopy was used for the first time to observe the explanted IOLs. The clinical aspect seemed to correspond to the phenomenon of surface light scattering, while laboratory analyses showed dense glistenings in the central layer of the IOL optic, which had no change next to the surface. Further studies on these phenomena are needed.

  19. Photovoltaic lifetime and degradation science statistical pathway development: acrylic degradation

    NASA Astrophysics Data System (ADS)

    Bruckman, Laura S.; Wheeler, Nicholas R.; Kidd, Ian V.; Sun, Jiayang; French, Roger H.

    2013-09-01

    In order to optimize and extend the life of photovoltaics (PV) modules, scienti c and mechanistic statistical analytics must be performed on a large sample of materials, components and systems. Statistically signi - cant relationships were investigated between di erent mechanistically based variables to develop a statistical pathway diagram for the degradation of acrylic that is important in concentrating photovoltaics. The statisti- cally signi cant relationships were investigated using lifetime and degradation science using a domain knowledge semi-supervised generalized structural equation modeling (semi-gSEM. Predictive analytics and prognostics are informed from the statistical pathway diagram in order to predictively understand the lifetime of PV modules in di erent stress conditions and help with these critical lifetime technologies.

  20. Chain Transfer of Vegetable Oil Macromonomers in Acrylic Solution Copolymerization

    SciTech Connect

    Black, Micah; Messman, Jamie M; Rawlins, James

    2011-01-01

    Use of vegetable oil macromonomers (VOMMs) as comonomers in emulsion polymerization enables good film coalescence without the addition of solvents that constitute volatile organic compounds (VOCs). VOMMs are derived from renewable resources and offer the potential of post-application crosslinking via auto-oxidation. However, chain transfer reactions of VOMMs with initiator and/or polymer radicals during emulsion polymerization reduce the amount of allylic hydrogen atoms available for primary auto-oxidation during drying. Vegetable oils and derivatives were reacted in combination with butyl acrylate and methyl methacrylate via solution polymerization. The copolymerization was monitored using in situ infrared spectroscopy to determine the extent of chain transfer. 1H NMR spectroscopy was used to determine the loci of chain transfer and the molecular weight characteristics of the polymers were characterized by SEC. Solution polymerization was utilized to minimize temperature fluctuations and maintain polymer solubility during the initial characterization.

  1. Impression techniques for multiple implants: a photoelastic analysis. Part II: comparison of four acrylic resins.

    PubMed

    Lopes-Júnior, Itamar; de Lima Lucas, Barbara; Gomide, Henner Alberto; Gomes, Vanderlei Luiz

    2013-10-01

    Four commercial brands of chemically activated acrylic resin were compared through photoelastic analysis. Photoelastic resin blocks were made with 2 implants placed parallel to each other and 2 square transfer copings splinted. Both transfers were splinted with chemically activated acrylic resin: Dencrilay, Duralay I, Duralay II, and GC. Data were analyzed by 2-way analysis of variance and Tukey test (P < .05). Statistically significant differences were found among the 3 brands of chemically activated acrylic resin. Dencrilay showed greater dimensional alteration. Duralay I and GC are recommended for the transfer of the position of the multi-implants.

  2. Crosslinked carboxymethylchitosan-g-poly(acrylic acid) copolymer as a novel superabsorbent polymer.

    PubMed

    Chen, Yu; Tan, Hui-min

    2006-05-22

    A novel carboxymethylchitosan-g-poly(acrylic acid) (CMCTS-g-PAA) superabsorbent polymer was prepared through graft polymerization of acrylic acid onto the chain of carboxymethylchitosan and subsequent crosslinking. It was demonstrated by FTIR spectroscopy that acrylic acid had been graft polymerized with carboxymethylchitosan. The thermal stability of the polymer was characterized by thermogravimetric analysis. By studying the swelling ratio of the polymer synthesized under different conditions, optimization conditions were found for a polymer with the highest swelling ratio. The rate of water absorption of the polymer was high, and the swelling of the polymer fitted the process of first dynamics. The swelling ratio of the polymer was pH-dependent.

  3. A Machine Vision Quality Control System for Industrial Acrylic Fibre Production

    NASA Astrophysics Data System (ADS)

    Heleno, Paulo; Davies, Roger; Correia, Bento A. Brázio; Dinis, João

    2002-12-01

    This paper describes the implementation of INFIBRA, a machine vision system used in the quality control of acrylic fibre production. The system was developed by INETI under a contract with a leading industrial manufacturer of acrylic fibres. It monitors several parameters of the acrylic production process. This paper presents, after a brief overview of the system, a detailed description of the machine vision algorithms developed to perform the inspection tasks unique to this system. Some of the results of online operation are also presented.

  4. Novel (meth)acrylate monomers for ultrarapid polymerization and enhanced polymer properties

    SciTech Connect

    Beckel, E. R.; Berchtold, K. A.; Nie, J.; Lu, H.; Stansbury, J. W.; Bowman, C. N.

    2002-01-01

    Ultraviolet light is known to be one of the most efficient methods to initiatc polymeric reactions in the presence of a photonitiator. Photopolymerizations are advantageous because the chemistry of the materials can be tailored to design liquid monomers for ultrarapid polymerization into a solid polymer material. One way to achieve rapid photopolymerizations is to utilize multifunctional (meth)acrylate monomers. which form highly crosslinked polymers; however, these monomers typically do not achieve complete functional group conversion. Recently, Decker et al. developed novel monovinyl acrylate monomers that display polyriicrization kinetics that rival those of multifunctional acrylate monomers. These novel acrylate monomers incorporate secondary functionalities and end groups such as carbonates, carbamates, cyclic carbonates and oxazolidone which promote the increased polymerization kinetics of these monomers. In addition to thc polynierization kinetics, these novel monovinyl monomers form crosslinked polymers, which are characterized by having high strength and high flexibility. Unfortunately, the exact mechanism or mechanisms responsible for the polymerization kinetics and crosslinking are not well understood.

  5. Synergistic effect of additives including multifunctional acrylates in wood plastic composites

    NASA Astrophysics Data System (ADS)

    Khan, Mubarak A.; Idriss Ali, K. M.; Garnett, John L.

    1993-07-01

    Wood Plastic Composite (WPC) was prepared with simul (soft wood, density = 0.4g/cc) and butylmethacrylate (BMA) monomer using 10% methanol as the swelling agent. Effect of additives including (i) multifunctional acrylates such as tripropylene glycol diacrylate (TPGDA), trimethylol propane triacrylate (TMPTA) (ii) oligomer acrylates like the urethane (UA), epoxy (EA) and polyester (PEA) acrylates and (iii) N-vinyl pyrrolidone (NVP) was investigated using 1 to 3 Mrad dose at 0.8 Mrad/h. Synergistic increases in polymer loading yields was achieved in presence of the additives, particularly with the trifunctional acrylate (TMPTA). In addition, acid as well as urea were also used as co-additives and synergistic enhancement in yields of polymer loading were obtained. The synergistic polymer loading by acid addition causes substantial decrease in tensile strength of the composite; but other additives and co-additives increase both the polymer loading and the tensile strength in these systems.

  6. Synthesis of acrylates. Quarterly progress report, April 1, 1995--June 30, 1995

    SciTech Connect

    1995-09-05

    The objective of this research is to develop a condensation/oxidation route for the synthesis of acrylates/methacrylates from coal-derived synthesis gas. This quarter work continued on the development of catalysts for propionate synthesis.

  7. Emulsion polymerization of polystyrene-co-acrylic acid with Cu2O incorporation

    NASA Astrophysics Data System (ADS)

    Fahmiati, Sri; Harmami, Sri Budi; Meliana, Yenny; Haryono, Agus

    2017-01-01

    In this research, poly(styrene-co-acrylic acid-Cu) was prepared via emulsion polymerization.Cu contents were varied as 10%, 15% and 20% and mol ratio of styrene to acrylic acid as 1:1 and 2:1. Structure and surface of poly(styrene-co-acrylic acid-Cu) were characterized by FTIR (Fourier Transformed Infra Red), NMR (Nuclear Magnetic Resonance), and SEM/EDX (Scanning Electron Microcope/ Energy Dispersive X-Ray) spectroscopy. The NMR spectra showed that the polymer was formed, however FTIR spectra showed that there were still unreacted monomers. SEM-EDX confirmed that copper (Cu) was dispersed uniformly on poly(styrene-co-acrylic acid-Cu) matrix.

  8. Biobased composites from thermoplastic polyurethane elastomer and cross-linked acrylated-epoxidized soybean oil

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Soybean oil is an important sustainable material. Crosslinked acrylated epoxidized soybean oil (AESO) is brittle without flexibility and the incorporation of thermoplastic polyurethane improves its toughness for industrial applications. The hydrophilic functional groups from both oil and polyurethan...

  9. Removal of methyl acrylate by ceramic-packed biotrickling filter and their response to bacterial community.

    PubMed

    Wu, Hao; Yin, Zhenhao; Quan, Yue; Fang, Yingyu; Yin, Chengri

    2016-06-01

    Methyl acrylate is a widely used raw chemical materials and it is toxic in humans. In order to treat the methyl acrylate waste gas, a 3-layer BTF packed with ceramic particles and immobilized with activated sludge was set up. The BTF exhibited excellent removal efficiency that no methyl acrylate could be detected when EBRT was larger than 266s and inlet concentration was lower than 0.19g/m(3). The 1st layer performed the best at fixed inlet concentration of 0.42g/m(3). PCR combined with DGGE was performed to detect the differences in different layers of the BTF. Phylum Proteobacteria (e.g. α-, β-, γ-, δ-) was predominantly represented in the bacterial community, followed by Actinobacteria and Firmicutes. Desulfovibrio gigas, Variovorax paradoxus, Dokdonella koreensis, Pseudoxanthomonas suwonensis, Azorhizobium caulinodans, Hyphomicrobium denitrificans, Hyphomicrobium sp. and Comamonas testosteroni formed the bacteria community to treat methyl acrylate waste gas in the BTF.

  10. In vitro cytotoxicity of self-curing acrylic resins of different colors

    PubMed Central

    Retamoso, Luciana Borges; da Cunha, Taís de Morais Alves; Pithon, Matheus Melo; dos Santos, Rogério Lacerda; Martins, Fernanda Otaviano; Romanos, Maria Teresa Villela; Tanaka, Orlando Motohiro

    2014-01-01

    Objective The aim of this study was to assess the in vitro cytotoxicity of acrylic resins of different colors over time. Methods Specimens were divided into 4 groups (n = 6) according to the color of the acrylic resin (Orto Class, Clássico, Campinas, São Paulo, Brazil): Group 1: clear acrylic resin; group 2: pink acrylic resin; group 3: blue acrylic resin and group 4: green acrylic resin. All specimens were fabricated according to the mass manipulation technique and submitted to mechanical polishing protocol. The control was performed with an amalgam specimen (C+), a glass specimen (C-) and cell control (CC). Specimens were immersed in Minimum Eagle's Medium (MEM) and incubated for 24 h at 37ºC. The extracts from the experimental material were filtered and mixed with L929 fibroblast. Cytotoxicity was evaluated at 4 different times, 24, 48, 72 and 168 h. After contact, cells were incubated for 24 h and added to 100 µ of 0.01% neutral red dye. The cells were incubated for 3 h for pigment incorporation and fixed. Cells viability was determined by a spectroscopic (BioTek, Winooski, Vermont, USA) with a 492-nm wavelength λ=492 nm). Results There were no statistical differences between the experimental groups and the CC and C- groups. Conclusion Clear, pink, blue and green self-curing acrylic resins fabricated by means of the mass manipulation technique and mechanically polished are not cytotoxic. Neither the pigment added to the self-curing acrylic resin nor the factor of time influenced the cytotoxicity of the material. PMID:25279523

  11. Investigation of a Relationship between Uniaxial and Biaxial Chemical Stress Crazing of Cast Acrylic

    DTIC Science & Technology

    1992-01-01

    number) FIELD GROUP SUB-GROUP Craze Initiation Chemical Craze Testing Uniaxial Stress Cast Acrylic Biaxial Stress Isopropyl Alcohol 19. ABSTRACT...cast acrylic with isopropyl alcohol . ASTM Standard Test Methods F484 and F1164 were used as guidelines for the uniaxial craze testing and biaxial...uniaxial and biaxial craze tests was conducted at various stress levels in conjunction with isopropyl alcohol . Isopropyl alcohol was the chosen chemical

  12. Color stability, water sorption and cytotoxicity of thermoplastic acrylic resin for non metal clasp denture

    PubMed Central

    Jang, Dae-Eun; Lee, Ji-Young; Jang, Hyun-Seon; Lee, Jang-Jae

    2015-01-01

    PURPOSE The aim of this study was to compare the color stability, water sorption and cytotoxicity of thermoplastic acrylic resin for the non-metal clasp dentures to those of thermoplastic polyamide and conventional heat-polymerized denture base resins. MATERIALS AND METHODS Three types of denture base resin, which are conventional heat-polymerized acrylic resin (Paladent 20), thermoplastic polyamide resin (Bio Tone), thermoplastic acrylic resin (Acrytone) were used as materials for this study. One hundred five specimens were fabricated. For the color stability test, specimens were immersed in the coffee and green tee for 1 and 8 weeks. Color change was measured by spectrometer. Water sorption was tested after 1 and 8 weeks immersion in the water. For the test of cytotoxicity, cell viability assay was measured and cell attachment was analyzed by FE-SEM. RESULTS All types of denture base resin showed color changes after 1 and 8 weeks immersion. However, there was no significant difference between denture base resins. All specimens showed significant color changes in the coffee than green tee. In water sorption test, thermoplastic acrylic resin showed lower values than conventional heat-polymerized acrylic resin and thermoplastic polyamide resin. Three types of denture base showed low cytotoxicity in cell viability assay. Thermoplastic acrylic resin showed the similar cell attachment but more stable attachment than conventional heat-polymerized acrylic resin. CONCLUSION Thermoplastic acrylic resin for the non-metal clasp denture showed acceptable color stability, water sorption and cytotoxicity. To verify the long stability in the mouth, additional in vitro studies are needed. PMID:26330974

  13. Testing of gloves for permeability to UV-curable acrylate coatings

    SciTech Connect

    Huggins, R.; Levy, N.; Pruitt, P.M.

    1987-07-01

    The handling of UV-curable acrylate formulations used in the coating of optical fiber requires protective measures to prevent contact dermatitis and/or allergic dermatitis. To characterize the permeability of various glove materials to a UV-curable acrylate coating, a study was undertaken using a modification of a standard ASTM permeability test, which demonstrated that nitrile rubber gloves provided the best protection of those glove materials tested.

  14. Continuous process of preparation of n-butyl(meth)acrylate by esterification of (meth)acrylic acid by butanol on thermostable sulfo-cation exchanger

    SciTech Connect

    Zheleznaya, L.L.; Karakhanov, R.A.; Lunin, A.F.; Magadov, R.S.; Meshcheryakov, S.V.; Mkrtychan, V.R.; Fomin, V.A.

    1987-11-10

    The authors propose an effective thermostable sulfo-cation exchanger based on polymers with a system of conjugated bonds, sulfopolyphenylene ketone (SPP) differing from the known cation exchangers by the high thermostability (up to 250/sup 0/C), and also having the effect of the stabilization of the double bond in unsaturated monomers. The combination of inhibiting and cation exchange properties makes it also possible to use these sulfo-cation exchangers in the processes of esterification of (meth)acrylic acids by alcohols without addition of special inhibitors. The SPP catalyst was tested in esterification processes of acrylic an methacrylic acid by butanol at a pilot plant.

  15. Radiopurity measurement of acrylic for the DEAP-3600 dark matter experiment

    NASA Astrophysics Data System (ADS)

    Nantais, Corina Michelle

    2014-05-01

    The liquid argon target of the DEAP-3600 dark matter detector is contained by an extremely radiopure acrylic vessel. Alpha decays from the inner surface of the acrylic vessel are a source of background. If a fraction of the alpha energy is observed, or if the recoiling nucleus from the alpha decay is observed, the event will not be separated from a dark matter candidate event. In addition to the low level of inherent contamination from uranium and thorium, the Pb-210 from Rn-222 diffusion during manufacturing must be measured. The limit for the DEAP-3600 acrylic vessel is 1.1 x 10-20 g/g Pb-210. By vaporizing a large quantity of acrylic and counting the concentrated residue with an ultralow background HPGe well detector and a low background alpha spectrometer, the bulk acrylic was found to have an upper limit of 10 -19 g/g Pb-210. The design, installation, commissioning, operation, and analysis for various aspects of the acrylic assay are described.

  16. Allergic contact dermatitis from sculptured acrylic nails: special presentation with an airborne pattern.

    PubMed

    Maio, Paula; Carvalho, Rodrigo; Amaro, Cristina; Santos, Raquel; Cardoso, Jorge

    2012-01-02

    Methylmethacrylate was first reported in 1941 as a cause of contact dermatitis. Since then, occupational contact allergies to acrylates in dentistry, orthopedic surgery, printing industry and industry have been reported, but few reports are found in the literature as a consequence of the contact with sculptured artificial acrylic nails which are increasingly popular. We describe here 3 patients with contact allergy to acrylates in artificial sculptured nails. Patch tests were performed with the Portuguese baseline series of contact allergens and an extended series of acrylates were applied. In particular, we tested three female patients with allergic contact dermatitis from sculptured acrylic nails. Two of these patients were both customers and also technical nail beauticians. Two patients developed periungual eczema; one presented only with face and eyelid dermatitis had no other lesions. The tests showed positive reaction to 2-hydroxyethylmethacrylate (2-HEMA) and 2-hydroxypropylmethacrylate (2-HPMA) in all the three patients. Our cases demonstrate the variety of clinical presentations of allergic contact dermatitis from acrylic sculptured nails. They show the need to warn patients of persistent and sometimes permanent side effects of these products. They also emphasize the importance of cosmetic ingredient labeling.

  17. Bone Marrow Nails Created by Percutaneous Osteoplasty for Long Bone Fracture: Comparisons Among Acrylic Cement Alone, Acrylic-Cement-Filled Bare Metallic Stent, and Acrylic-Cement-Filled Covered Metallic Stent

    SciTech Connect

    Nakata, Kouhei; Kawai, Nobuyuki; Sato, Morio Cao, Guang; Sahara, Shinya; Sonomura, Tetsuo; Takasaka, Isao; Minamiguchi, Hiroki; Nakai, Motoki

    2011-06-15

    Purpose: This study was designed to compare the strength among bone marrow nails created to treat long bone fractures using interventional procedures. Methods: Twelve resected intact tibiae of healthy swine were used. A circumferential bone fracture was made in nine tibiae and restored with the following created bone marrow nails: acrylic cement alone (ACA) (n = 3), acrylic-cement-filled bare metallic stent (AC-FBMS) (n = 3), and acrylic-cement-filled covered metallic (AC-FCMS) stent (n = 3). The remaining intact tibiae (n = 3) were used as controls. Results: A bone marrow nail was successfully achieved within 30 min in all swine. The maximum injection volume of acrylic cement for creating ACA, AC-FBMS, and AC-FCMS was 1.7 {+-} 0.3, 3.2 {+-} 0.4, and 2.9 {+-} 0.4 mL, respectively. The thickness of bone marrow nail created in the ACA, AC-FBMS, and AC-FCMS groups was 3.6 {+-} 1.0, 10.3 {+-} 0.26, and 9.6 {+-} 0.32 mm, respectively (AC-FBMS group versus AC-FCMS group, p = 0.038), probably because of leakage of acrylic cement surrounding the interstices. The maximum bending power (kilonewton) and bending strength (newton/mm{sup 2}) in the normal long bone, ACA, AC-FBMS, and AC-FCMS groups were: 1.70 {+-} 0.25 and 79.2 {+-} 16.1; 0.21 {+-} 0.11 and 8.8 {+-} 2.8; 0.46 {+-} 0.06 and 18.2 {+-} 1.6; and 0.18 {+-} 0.04 and 7.8 {+-} 2.7, respectively. Conclusions: Although the maximum bending power and bending strength of AC-FBMS were not satisfactory, it was the most robust of the three marrow nails for restoring fractured long bone.

  18. Antibacterial Adhesion of Polymethyl Methacrylate Modified by Borneol Acrylate.

    PubMed

    Sun, Xueli; Qian, Zhiyong; Luo, Lingqiong; Yuan, Qipeng; Guo, Ximin; Tao, Lei; Wei, Yen; Wang, Xing

    2016-10-07

    Polymethyl methacrylate (PMMA) is a widely used biomaterial. But there is still a challenge facing its unwanted bacterial adhesion, because the subsequent biofilm formation usually leads to failure of related implants. Herein, we present a borneol-modified PMMA based on a facile and effective stereochemical strategy, generating antibacterial copolymer named as P(MMA-co-BA). It was synthesized by free radical polymerization and studied with different ratio between methyl methacrylate (MMA) and borneol acrylate (BA) monomers. NMR, GPC and EA etc. were used to confirm their chemical features. Their films were challenged with Escherichia coli (Gram-negative) and Bacillus subtilis (Gram-positive), showing a BA content-dependent antibacterial performance. The minimum effective dose should be 10%. Then in vivo subcutaneous implantations in mice demonstrated their biocompatibilities through routine histotomy and HE staining. Therefore, P(MMA-co-BA)s not only exhibited their unique antibacterial character, but also suggested a potential for the safe usage of borneol-modified PMMA frame and devices for further implantation.

  19. Injectable acrylic bone cements for vertebroplasty with improved properties.

    PubMed

    Carrodeguas, Raúl García; Lasa, Blanca Vázquez; Del Barrio, Julio San Román

    2004-01-15

    Currently commercially available acrylic bone cements lack adequate radiopacity and viscosity when they are used in percutaneous vertebroplasty (PVP). In this work improved formulations of radiopaque and injectable poly(methyl methacrylate) bone cements were prepared with different amounts (10-50 wt.%) of BaTiO3 or SrTiO3 particles as the radiopaque agent. Two sets of cements were prepared by using untreated or silanated radiopaque particles, respectively. The influence of the content and nature of the radiopaque agent as well as its silanation with 3-(trimethoxysilyl) propyl methacrylate (gamma-MPS), on the curing parameters, residual monomer content, radiopacity, mechanical properties, and injectability of the resulting materials, was examined. Doughing and setting times, maximum temperature, and compressive strength of all formulations fulfilled the requirements of standard specifications, with values of peak temperature in the range 57-72 degrees C and those of compressive strength between 114 and 135 MPa. Formulations containing at least 20 wt.% BaTiO3 or SrTiO3 had radiopacities equal to or greater than that corresponding to 2 mm of Al as required for surgical plastics. Injectability of any of the formulations provided 75-80 wt.% of the total mass manually injected through a conventional biopsy needle 4 min after mixing. Silanation of the BaTiO3 or SrTiO3 particles led to formulations with improved mechanical properties and injectability compared to those obtained with the untreated fillers.

  20. Synthesis of acrylates and methacrylates from coal-derived syngas

    SciTech Connect

    Spivey, J.J.; Gogate, M.R.; Jang, B.W.L.

    1995-12-31

    Acrylates and methacrylates are among the most widely used chemical intermediates in the world. One of the key chemicals of this type is methyl methacrylate. Of the 4 billion pounds produced each year, roughly 85% is made using the acetone-cyanohydrin process, which requires handling of large quantities of hydrogen cyanide and produces ammonium sulfate wastes that pose an environmental disposal challenge. The U.S. Department of Energy and Eastman Chemical Company are sharing the cost of research to develop an alternative process for the synthesis of methyl methacrylate from syngas. Research Triangle Institute is focusing on the synthesis and testing of active catalysts for the condensation reactions, and Bechtel is analyzing the costs to determine the competitiveness of several process alternatives. Results thus far show that the catalysts for the condensation of formaldehyde and the propionate are key to selectively producing the desired product, methacrylic acid, with a high yield. These condensation catalysts have both acid and base functions and the strength and distribution of these acid-base sites controls the product selectivity and yield.

  1. Impact initiation of reactive aluminized fluorinated acrylic nanocomposites

    SciTech Connect

    White, Bradley W.; Crouse, Christopher A.; Spowart, Jonathan E.; Aydelotte, Brady; Thadhani, Naresh N.

    2016-04-18

    The initiation of aluminized fluorinated acrylic (AlFA) nanocomposites during modified Taylor impact tests was investigated. Samples were impacted against a steel or sapphire anvil at a nominal velocity of 150 m/s. A framing camera was used to capture head-on and side-profile impact images for the sapphire window and steel plate rigid anvils, respectively. Correlations were drawn between both experimental setups to determine the initiation locations and reaction times. Reactions were found to initiate at an intermediate radius on the impact face of the pellet at a time near full compaction. From simulations, the highest strains and temperatures were found at radii similar to those observed in experiments at the time of ignition. Off-normal impacts produced higher localized straining and temperatures on one-half of the pellet. As a result, the copper projectile, used for delivery, was revealed to aid in a shear assisted reaction by helping to drive the pellet material outward as the projectile deformed radially.

  2. Impact initiation of reactive aluminized fluorinated acrylic nanocomposites

    DOE PAGES

    White, Bradley W.; Crouse, Christopher A.; Spowart, Jonathan E.; ...

    2016-04-18

    The initiation of aluminized fluorinated acrylic (AlFA) nanocomposites during modified Taylor impact tests was investigated. Samples were impacted against a steel or sapphire anvil at a nominal velocity of 150 m/s. A framing camera was used to capture head-on and side-profile impact images for the sapphire window and steel plate rigid anvils, respectively. Correlations were drawn between both experimental setups to determine the initiation locations and reaction times. Reactions were found to initiate at an intermediate radius on the impact face of the pellet at a time near full compaction. From simulations, the highest strains and temperatures were found atmore » radii similar to those observed in experiments at the time of ignition. Off-normal impacts produced higher localized straining and temperatures on one-half of the pellet. As a result, the copper projectile, used for delivery, was revealed to aid in a shear assisted reaction by helping to drive the pellet material outward as the projectile deformed radially.« less

  3. Cytocompatible antifungal acrylic resin containing silver nanoparticles for dentures

    PubMed Central

    Acosta-Torres, Laura Susana; Mendieta, Irasema; Nuñez-Anita, Rosa Elvira; Cajero-Juárez, Marcos; Castaño, Víctor M

    2012-01-01

    Background Inhibition of Candida albicans on denture resins could play a significant role in preventing the development of denture stomatitis. The safety of a new dental material with antifungal properties was analyzed in this work. Methods Poly(methyl methacrylate) [PMMA] discs and PMMA-silver nanoparticle discs were formulated, with the commercial acrylic resin, Nature-CrylTM, used as a control. Silver nanoparticles were synthesized and characterized by ultraviolet-visible spectroscopy, dispersive Raman spectroscopy, and transmission electron microscopy. The antifungal effect was assessed using a luminescent microbial cell viability assay. Biocompatibility tests were carried out using NIH-3T3 mouse embryonic fibroblasts and a Jurkat human lymphocyte cell line. Cells were cultured for 24 or 72 hours in the presence or absence of the polymer formulations and analyzed using three different tests, ie, cellular viability by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and cell proliferation by enzyme-linked immunosorbent assay BrdU, and genomic DNA damage (Comet assay). Finally, the samples were evaluated mechanically, and the polymer-bearing silver nanoparticles were analyzed microscopically to evaluate dispersion of the nanoparticles. Results The results show that PMMA-silver nanoparticle discs significantly reduce adherence of C. albicans and do not affect metabolism or proliferation. They also appear not to cause genotoxic damage to cells. Conclusion The present work has developed a new biocompatible antifungal PMMA denture base material. PMID:22969297

  4. Interaction of photosensitive surfactant with DNA and poly acrylic acid

    SciTech Connect

    Zakrevskyy, Yuriy Paasche, Jens; Lomadze, Nino; Santer, Svetlana; Cywinski, Piotr; Cywinska, Magdalena; Reich, Oliver; Löhmannsröben, Hans-Gerd

    2014-01-28

    In this paper, we investigate interactions and phase transitions in polyelectrolyte-surfactant complexes formed between a cationic azobenzene-containing surfactant and two types of polyelectrolytes: natural (DNA) or synthetic (PAA: poly acrylic acid). The construction of a phase diagram allowed distancing between four major phases: extended coil conformation, colloidally stable compacted globules, colloidal instability range, and surfactant-stabilized compact state. Investigation on the complexes’ properties in different phases and under irradiation with UV light provides information about the role of the surfactant's hydrophobic trans isomers both in the formation and destruction of DNA and PAA globules as well as in their colloidal stabilization. The trans isomer shows much stronger affinity to the polyelectrolytes than the hydrophilic cis counterpart. There is no need for complete compensation of the polyelectrolyte charges to reach the complete compaction. On contrary to the findings previously reported in the literature, we demonstrate – for the first time – complete polyelectrolyte compaction which occurs already at 20% of DNA (and at 50% of PAA) charge compensation. The trans isomer plays the main role in the compaction. The aggregation between azobenzene units in the photosensitive surfactant is a driving force of this process. The decompaction can be realized during UV light irradiation and is strongly influenced by the interplay between surfactant-surfactant and surfactant-DNA interactions in the compacted globules.

  5. Poly(1-adamantyl acrylate): Living Anionic Polymerization, Block Copolymerization, and Thermal Properties

    DOE PAGES

    Lu, Wei; Huang, Caili; Hong, Kunlun; ...

    2016-12-06

    Living anionic polymerization of acrylates is challenging due to intrinsic side reactions including backbiting reactions of propagating enolate anions and aggregation of active chain ends. In this study, the controlled synthesis of poly(1-adamatyl acrylate) (PAdA) was performed successfully for the first time via living anionic polymerization through investigation of the initiation systems of sec-butyllithium/diphenylethylene/lithium chloride (sec-BuLi/DPE/LiCl), diphenylmethylpotassium/diethylzinc (DPMK/Et2Zn), and sodium naphthalenide/dipenylethylene/diethylzinc (Na-Naph/DPE/Et2Zn) in tetrahydrofuran at -78 °C using custom glass-blowing and high-vacuum techniques. PAdA synthesized via anionic polymerization using DPMK with a large excess (more than 40-fold to DPMK) of Et2Zn as the ligand exhibited predicted molecular weights from 4.3more » to 71.8 kg/mol and polydispersity indices of around 1.10. In addition, the produced PAdAs exhibit a low level of isotactic content (mm triads of 2.1%). The block copolymers of AdA and methyl methacrylate (MMA) were obtained by sequential anionic polymerization, and the distinct living property of PAdA over other acrylates was demonstrated based on the observation that the resulting PAdA-b-PMMA block copolymers were formed with no residual PAdA homopolymer. The PAdA homopolymers exhibit a very high glass transition temperature (133 °C) and outstanding thermal stability (Td: 376 °C) as compared to other acrylic polymers such as poly(tert-butyl acrylate) and poly(methyl acrylate). These merits make PAdA a promising candidate for acrylic-based thermoplastic elastomers with high upper service temperature and enhanced mechanical strength.« less

  6. Poly(1-adamantyl acrylate): Living Anionic Polymerization, Block Copolymerization, and Thermal Properties

    SciTech Connect

    Lu, Wei; Huang, Caili; Hong, Kunlun; Kang, Nam-Goo; Mays, Jimmy W.

    2016-12-06

    Living anionic polymerization of acrylates is challenging due to intrinsic side reactions including backbiting reactions of propagating enolate anions and aggregation of active chain ends. In this study, the controlled synthesis of poly(1-adamatyl acrylate) (PAdA) was performed successfully for the first time via living anionic polymerization through investigation of the initiation systems of sec-butyllithium/diphenylethylene/lithium chloride (sec-BuLi/DPE/LiCl), diphenylmethylpotassium/diethylzinc (DPMK/Et2Zn), and sodium naphthalenide/dipenylethylene/diethylzinc (Na-Naph/DPE/Et2Zn) in tetrahydrofuran at -78 °C using custom glass-blowing and high-vacuum techniques. PAdA synthesized via anionic polymerization using DPMK with a large excess (more than 40-fold to DPMK) of Et2Zn as the ligand exhibited predicted molecular weights from 4.3 to 71.8 kg/mol and polydispersity indices of around 1.10. In addition, the produced PAdAs exhibit a low level of isotactic content (mm triads of 2.1%). The block copolymers of AdA and methyl methacrylate (MMA) were obtained by sequential anionic polymerization, and the distinct living property of PAdA over other acrylates was demonstrated based on the observation that the resulting PAdA-b-PMMA block copolymers were formed with no residual PAdA homopolymer. The PAdA homopolymers exhibit a very high glass transition temperature (133 °C) and outstanding thermal stability (Td: 376 °C) as compared to other acrylic polymers such as poly(tert-butyl acrylate) and poly(methyl acrylate). These merits make PAdA a promising candidate for acrylic-based thermoplastic elastomers with high upper service temperature and enhanced mechanical strength.

  7. The effect of various frequencies of ultrasonic cleaner in reducing residual monomer in acrylic resin.

    PubMed

    Charasseangpaisarn, Taksid; Wiwatwarrapan, Chairat

    2015-12-01

    Monomer remaining in denture base acrylic can be a major problem because it may cause adverse effects on oral tissue and on the properties of the material. The purpose of this study was to compare the effect of various ultrasonic cleaner frequencies on the amount of residual monomer in acrylic resin after curing. Forty-two specimens each of Meliodent heat-polymerized acrylic resin (M) and Unifast Trad Ivory auto-polymerized acrylic resin (U) were prepared according to their manufacturer's instructions and randomly divided into seven groups: Negative control (NC); Positive control (PC); and five ultrasonic treatment groups: 28 kHz (F1), 40 kHz (F2), 60 kHz (F3) (M=10 min, U=5 min), and 28 kHz followed by 60 kHz (F4: M=5 min per frequency, U=2.5 min per frequency, and F5: M=10 min followed by 5 min per frequency, U=5 min followed by 2.5 min per frequency). Residual monomer was determined by HPLC following ISO 20795-1. The data were analyzed by One-way ANOVA and Tukey HSD. There was significantly less residual monomer in the auto-polymerized acrylic resin in all ultrasonic treatment groups and the PC group than that of the NC group (p<0.05). However, the amount of residual monomer in group F3 was significantly higher than that of the F1, F4, and PC groups (p<0.05). In contrast, ultrasonic treatment did not reduce the amount of residual monomer in heat-polymerized acrylic resin (p>0.05). The amount of residual monomer in heat-polymerized acrylic resin was significantly lower than that of auto-polymerized acrylic resin. In conclusion, ultrasonic treatment at low frequencies is recommended to reduce the residual monomer in auto-polymerized acrylic resin and this method is more practical in a clinical situation than previously recommended methods because of reduced chairside time.

  8. Focal point analysis of torsional isomers of acrylic acid

    NASA Astrophysics Data System (ADS)

    Alev Çiftçioğlu, Gökçen; Trindle, Carl; Yavuz, Ilhan

    2010-10-01

    The thermochemistry of acrylic acid has presented challenges owing to its high reactivity, tendency to dimerize in the gas phase, and the existence of two very nearly equal energy conformational isomers. Well-tested thermochemical schemes including G2, G3, G4, and CBS-QB3 agree in the prediction that the s-cis syn structure is the most stable of the torsional isomers, with the s-cis anti form lying 3 kJ mol-1 or less higher in energy. Microwave spectra suggest a value of 0.63 kJ mol-1. The energy barrier between these forms is in the neighbourhood of 25 kJ mol-1 according to a MP2/cc-pVDZ calculation. We present estimates of the relative energies of all four torsional isomers and the rotational barrier based on a variant of the Focal Point Analysis developed by Császár and co-workers. These calculations, extending to the CCSD(T)/cc-pV5Z level, predict that the s-cis anti torsional isomer is the most stable form, in contrast to prior estimates. The s-cis syn form lies about 2.9 kJ mol-1 higher, while the s-trans syn and anti forms lie at about 21.7 and 23.3 kJ mol-1, respectively. We estimate the rotational barrier between the s-cis trans and s-cis anti structures to be about 23.9 kJ mol-1. Error ranges derived from the fit to extrapolation forms suggest that our estimates have an uncertainty of about 0.1 kJ mol-1.

  9. Supercritical water oxidation of acrylic acid production wastewater.

    PubMed

    Gong, Y M; Wang, S Z; Tang, X Y; Xu, D H; Ma, H H

    2014-01-01

    Supercritical water oxidation (SCWO) of wastewater from an acrylic acid manufacturing plant has been studied on a continuous flow experimental system, whose reactor was made of Hastelloy C-276. Experimental conditions included a reaction temperature (T) ranging from 673 to 773K, a residence time (t) ranging from 72.7 to 339s, a constant pressure (P) of 25 MPa and a fixed oxidation coefficient (alpha) of 2.0. Experimental results indicated that reaction temperature and residence time had significant influences on the oxidation reaction, and increasing the two operation parameters could improve both degradation of chemical oxygen demand (COD) and ammonia nitrogen (NH3-N). The COD removal efficiency could reach up to 98.73% at 25 MPa, 773 K and 180.1 s, whereas the destruction efficiency of NH3-N was only 43.71%. We further carried out a kinetic analysis considering the induction period through free radical chain mechanism. It confirms that the power-law rate equation for COD removal was 345 exp(-52200/RT)[COD]1.98[O2]0.17 and for NH3-N removal was 500 exp(-64492.19/RT)[NH3-N]1.87 [O2]0.03. Moreover, the induction time formulations for COD and NH3-N were suspected to be exp(38250/RT)/173 and exp(55690/RT)/15231, respectively. Correspondingly, induction time changed from 2.22 to 5.38 s for COD and 0.38 to 1.38 s for NH3-N. Owing to the catalysis of reactor inner wall surface, more than 97% COD removal was achieved in all samples.

  10. Conversion of (Meth)acrylic acids to methane granular sludge: Initiation by specific anerobic microflora

    SciTech Connect

    Shtarkman, N.B.; Obraztova, A.Y.; Laurinavichyus, K.S.; Galushko, A.S.; Akimenko, V.K.

    1995-03-01

    The role of a specific anaerobic microflora in the initiation of degradation of (meth)acrylic acids to methane by granular sludge from a UASB reactor was investigated. Associations of anaerobic bacteria isolated from the anaerobic sludge, which was used for a long time for treatment of wastewater from (meth)acrylate production, were able to realize the initial stage of (meth)acrylic acid decomposition, i.e., a conversion of acrylic and methacrylic acids to propionic and isobutyric acids, respectively. When added to granules, these association played a role of an {open_quotes}initiator{close_quotes} of the degradation process, which was then continued by the granular sludge microflora utilizing propionate and isobutyrate. Some characteristics of the granules adapted to propionate or isobutyrate are presented. The rates of propionate and isobutyrate consumption by adapted granules is, respectively, 21 and 53 times higher than the values obtained for nonadapted granules. A combined use of {open_quotes}initiating{close_quotes} bacteria and adapted granules provided degradation of (meth)acrylic acids with a maximum methane yield. The possibility is discussed of employing the granules, which are adapted to short-chain fatty acids, and the {open_quotes}initiating{close_quotes} bacteria, which accomplish the initial steps of the organic material decomposition to lower fatty acids, for the conversion of various chemical compounds to methane. 10 refs., 3 figs., 2 tabs.

  11. The electrospinning of the copolymer of styrene and butyl acrylate for its application as oil absorbent.

    PubMed

    Xu, Naiku; Cao, Jipeng; Lu, Yuyao

    2016-01-01

    Electrospun polystyrene materials have been employed as oil absorbents, but they have visible drawbacks such as poor strength at low temperature and unreliable integrity because of brittleness and insufficient cohesive force among fibers. Butyl acrylate can polymerize into flexible chains, and its polymer can be used as elastomer and adhesive material. Thereby it is possible to obtain the material that has better performance in comparison with electrospun polystyrene material through the electrospinning of the copolymer of styrene and butyl acrylate. In this work, a polymer was synthesized through suspension polymerization by using styrene and butyl acrylate as comonomers. The synthesis of the copolymer of styrene and butyl acrylate was verified through dissolution and hydrolysis experimental data; as well through nuclear magnetic resonance spectrometry. The viscous flow activation energy of the solution consisting of copolymer and N, N-dimethylformamide was determined via viscosity method and then adopted to establish the entanglement characteristics of butyl acrylate's chain segments. Finally, in order to electrospin the copolymer solution into fibrous membrane, the effects of monomer feed ratio and spinning parameters were investigated. The prepared fibrous membrane was found to have a potential use as oil absorbent.

  12. Radiation modification of water absorption of cassava starch by acrylic acid/acrylamide

    NASA Astrophysics Data System (ADS)

    Kiatkamjornwong, Suda; Chomsaksakul, Wararuk; Sonsuk, Manit

    2000-10-01

    Graft copolymerizations of acrylamide and/or acrylic acid onto cassava starch by a simultaneous irradiation technique using gamma-rays as the initiator were studied with regard to various parameters of importance: the monomer-to-cassava starch ratio, total dose (kGy), dose rate (kGy h -1), acrylamide-to-acrylic acid ratio, and the addition of nitric acid and maleic acid as the additives. Grafting parameters were determined in relation to the water absorption of the saponified graft copolymer. The water absorption of the saponified graft copolymer in salt and buffer solutions of different ionic strengths was also measured, from which the superabsorbent properties are found to be pH sensitive. The starch graft copolymers of acrylamide and acrylic acid give higher water absorption than the starch graft copolymers of either acrylamide or acrylic acid alone. The porosity of the saponified starch graft copolymers prepared by the acrylamide/acrylic acid ratios of 70:30 and 50:50 was much higher than the porosity of copolymers in terms of fine networks. Ionic strength and multi-oxidation states of the saline and buffer solutions markedly decreased the water absorption of the saponified cassava starch grafted superabsorbent polymers.

  13. The antimicrobial effect of benzalkonium chloride on some pathogenic microbes observed on fibers of acrylic carpet.

    PubMed

    Khajavi, Ramin; Sattari, Morteza; Ashjaran, Ali

    2007-02-15

    In the presented research, the main aim is to investigate the antibacterial effectiveness of BAC solutions on acrylic fibers used in machinery carpet. An acrylic pile carpet laid in a public place for 30 days and the existence of some microbes were investigated on it. The antimicrobial effect of different BAC solutions for identified microbes was studied in vitro. The acrylic fibers were treated with the same different solutions of BAC as before and the antibacterial effectiveness was assessed by the zone of inhibition method in different times. Two pieces of carpet untreated and treated with BAC solution sewed together and laid for one week in the public place and the amounts of bacterial growth determined by colony count method and the results compared. Finally some mechanical properties of treated acrylic fibers measured after 30 days and compared with untreated one. The results showed the presence of some pathogenic microbes on the laid carpet such as Escherichia coli and Staphylococcus aureus. The inhalation time for treated acrylic fibers improved. The amount of colony growth on treated carpet reduced considerably and besides the mechanical tests results showed no significant deterioration effect of studied properties in comparing with untreated yarn.

  14. Comparison of impact strength of acrylic resin reinforced with kevlar and polyethylene fibres.

    PubMed

    Kamath, G; Bhargava, K

    2002-01-01

    The present study was done to evaluate the impact strengths of heat-activated acrylic resins reinforced with Kevlar fibres, polyethylene fibres and unreinforced heat activated acrylic resin. Each of three groups had 25 specimens. Brass rods of uniform length of 40 mm and diameter of 8 mm were used to prepare the moulds. A combination of long fibres (40 mm length) and short fibres (6 mm length) were used. The total amount of fibres incorporated was limited to 2% by weight of the resin matrix. Short and long fibres of equal weight were incorporated. The short fibres were mixed with polymer and monomer and packed into the mould, while, the long axis of the specimen, perpendicular to the applied force. The specimens were then processed. Impact strength testing was done on Hounsfield's impact testing machine. Kevlar fibre reinforced heat activated acrylic resin specimens recorded higher mean impact strength of 0.8464 Joules, while polyethylene fibres reinforced heat activated acrylic resin recorded mean impact strength of 0.7596 joules. The unreinforced heat activated acrylic resin recorded mean impact strength of 0.3440 Joules.

  15. Hybrid thiol-ene network nanocomposites based on multi(meth)acrylate POSS.

    PubMed

    Li, Liguo; Liang, Rendong; Li, Yajie; Liu, Hongzhi; Feng, Shengyu

    2013-09-15

    First, multi(meth)acrylate functionalized POSS monomers were synthesized in this paper. Secondly, FTIR was used to evaluate the homopolymerization behaviors of multi(meth)acrylate POSS and their copolymerization behaviors in the thiol-ene reactions with octa(3-mercaptopropyl) POSS in the presence of photoinitiator. Results showed that the photopolymerization rate of multimethacrylate POSS was faster than that of multiacrylate POSS. The FTIR results also showed that the copolymerizations were dominant in the thiol-ene reactions with octa(3-mercaptopropyl) POSS, different from traditional (meth)acrylate-thiol system, in which homopolymerizations were predominant. Finally, the resulted hybrid networks based on POSS were characterized by XRD, FE-SEM, DSC, and TGA. The characterization results showed that hybrid networks based on POSS were homogeneous and exhibited high thermal stability.

  16. Catalytic production of methyl acrylates by gold-mediated cross coupling of unsaturated aldehydes with methanol

    NASA Astrophysics Data System (ADS)

    Karakalos, Stavros; Zugic, Branko; Stowers, Kara J.; Biener, Monika M.; Biener, Juergen; Friend, Cynthia M.; Madix, Robert J.

    2016-10-01

    Modern methods of esterification, one of the most important reactions in organic synthesis, are reaching their limits, as far as waste and expense are concerned. Novel chemical approaches to ester formation are therefore of importance. Here we report a simple procedure free of caustic reagents or byproducts for the facile direct oxidative methyl esterification of aldehydes over nanoporous Au catalysts. Complementary model studies on single crystal gold surfaces establish the fundamental reactions involved. We find that methanol more readily reacts with adsorbed active oxygen than do the aldehydes, but that once the aldehydes do react, they form strongly-bound acrylates that block reactive sites and decrease the yields of acrylic esters under steady flow conditions at 420 K. Significant improvements in yield can be achieved by operating at higher temperatures, which render the site-blocking acrylates unstable.

  17. Radiation synthesis of superabsorbent poly(acrylic acid)-carrageenan hydrogels

    NASA Astrophysics Data System (ADS)

    Francis, Sanju; Kumar, Manmohan; Varshney, Lalit

    2004-04-01

    A series of superabsorbent hydrogels were prepared from carrageenan and partially neutralized acrylic acid by gamma irradiation at room temperature. The gel fraction, swelling kinetics and the equilibrium degree of swelling (EDS) of the hydrogels were studied. It was found that the incorporation of even 1% carrageenan (sodium salt) increases the EDS of the hydrogels from ˜320 to ˜800 g/g. Thermal analysis were carried out to determine the amount of free water and bound water in the hydrogels. Under optimum conditions, poly(acrylic acid)-carrageenan hydrogels with high gel fraction (˜80%) and very high EDS (˜800 g/g) were prepared gamma radiolytically from aqueous solution containing 15% partially neutralized acrylic acid and 1-5% carrageenan. The hydrogels were also found to be sensitive to the pH and the ionic strength of the medium.

  18. Synthesis of radiation crosslinked poly(acrylic acid) in the presence of phenyltriethoxysilane

    NASA Astrophysics Data System (ADS)

    Hassan, Safia; Yasin, Tariq

    2014-04-01

    Acrylic acid based superabsorbent hydrogel was prepared using phenyltriethoxysilane (PTES) as polyfunctional monomer. Different amounts of PTES were incorporated in acrylic acid and irradiated at different doses upto maximum of 30 kGy. The crosslinked acrylic acid showed hydrogel properties and its swelling kinetics, gel fraction and equilibrium degree of swelling (EDS) were studied. It was found that the increased PTES concentration decreased the EDS of the hydrogels. Infrared spectroscopy confirmed the crosslinking reaction between the feed components and the existence of siloxane bond. Thermogravimetric analysis showed an increase in the stability of the hydrogels having high PTES content. The swelling of the hydrogel was affected by pH, ionic strength and temperature. These hydrogels showed low swelling in acidic and basic pH range and high swelling around neutral pH. This switchable pH response of these hydrogels can be exploited in environmental and biomedical applications.

  19. New blends of ethylene-butyl acrylate copolymers with thermoplastic starch. Characterization and bacterial biodegradation.

    PubMed

    Morro, A; Catalina, F; Corrales, T; Pablos, J L; Marin, I; Abrusci, C

    2016-09-20

    Ethylene-butyl acrylate copolymer (EBA) with 13% of butyl acrylate content was used to produce blends with 10, 30 and 60% of thermoplastic starch (TPS) plasticized with glycerol. Ethylene-acrylic acid copolymer (EAA) was used as compatibilizer at 20% content with respect to EBA. The blends were characterized by X-ray diffraction, ATR-Fourier Transform Infrared Spectroscopy (ATR-FTIR), Scanning Electron Microscopy (SEM), water-Contact Angle measurements (CA), Differential Scanning Calorimetry (DSC) and Stress-strain mechanical tests. Initiated autoxidation of the polymer blends was studied by chemiluminescence (CL) confirming that the presence of the polyolefin-TPS interphase did not substantially affect the oxidative thermostability of the materials. Three bacterial species have been isolated from the blend films buried in soil and identified as Bacillus subtilis, Bacillus borstelensis and Bacillus licheniformis. Biodegradation of the blends (28days at 45°C) was evaluated by carbon dioxide measurement using the indirect impedance technique.

  20. Synthesis of acrylic and allylic bifunctional cross-linking monomers derived from PET waste

    NASA Astrophysics Data System (ADS)

    Cruz-Aguilar, A.; Herrera-González, A. M.; Vázquez-García, R. A.; Navarro-Rodríguez, D.; Coreño, J.

    2013-06-01

    An acrylic and two novel allylic monomers synthesized from bis (hydroxyethyl) terephthalate, BHET, are reported. This was obtained by glycolysis of post-consumer PET with boiling ethylene glycol. The bifunctional monomer bis(2-(acryloyloxy)ethyl) terephthalate was obtained from acryloyl chloride, while the allylic monomers 2-(((allyloxi)carbonyl)oxy) ethyl (2-hydroxyethyl) terephthalate and bis(2-(((allyloxi)carbonyl)oxy)ethyl) terephthalate, from allyl chloroformate. Cross-linking was studied in bulk polymerization using two different thermal initiators. Monomers were analyzed by means of 1H NMR and the cross-linked polymers by infrared spectroscopy. Gel content higher than 90% was obtained for the acrylic monomer. In the case of the mixture of the allylic monomers, the cross-linked polymer was 80 % using BPO initiator, being this mixture 24 times less reactive than the acrylic monomer.

  1. Nitrile Hydratase and Amidase from Rhodococcus rhodochrous Hydrolyze Acrylic Fibers and Granular Polyacrylonitriles

    PubMed Central

    Tauber, M. M.; Cavaco-Paulo, A.; Robra, K.-H.; Gübitz, G. M.

    2000-01-01

    Rhodococcus rhodochrous NCIMB 11216 produced nitrile hydratase (320 nkat mg of protein−1) and amidase activity (38.4 nkat mg of protein−1) when grown on a medium containing propionitrile. These enzymes were able to hydrolyze nitrile groups of both granular polyacrylonitriles (PAN) and acrylic fibers. Nitrile groups of PAN40 (molecular mass, 40 kDa) and PAN190 (molecular mass, 190 kDa) were converted into the corresponding carbonic acids to 1.8 and 1.0%, respectively. In contrast, surfacial nitrile groups of acrylic fibers were only converted to the corresponding amides. X-ray photoelectron spectroscopy analysis showed that 16% of the surfacial nitrile groups were hydrolyzed by the R. rhodochrous enzymes. Due to the enzymatic modification, the acrylic fibers became more hydrophilic and thus, adsorption of dyes was enhanced. This was indicated by a 15% increase in the staining level (K/S value) for C.I. Basic Blue 9. PMID:10742253

  2. The effect of different polishing techniques on the surface roughness of acrylic resin materials.

    PubMed

    Sofou, A; Emmanouil, J; Peutzfeldt, A; Owall, B

    2001-01-01

    This study evaluated three methods of surface polishing on acrylic denture base materials. Specimens of three commercial heat-cured acrylic resin materials were finished using burs, sandpaper discs and rubber wheels, and polished with polishing soap, paste, or by application of a UV-light-activated resin sealant. The resulting surface roughness was examined by scanning electron microscopy as well as measured by means of a stylus profile Perthometer. Surface roughness was reduced by polishing. Polishing paste and UV-light-activated resin sealant were more, and equally, effective in reducing surface roughness compared to polishing soap. Polishing paste or UV-light-activated resin sealant may be used to create a smoother surface on acrylic dentures.

  3. Evaluation of Liquid-Liquid Extraction Process for Separating Acrylic Acid Produced From Renewable Sugars

    NASA Astrophysics Data System (ADS)

    Alvarez, M. E. T.; Moraes, E. B.; Machado, A. B.; Maciel Filho, R.; Wolf-Maciel, M. R.

    In this article, the separation and the purification of the acrylic acid produced from renewable sugars were studied using the liquid-liquid extraction process. Nonrandom two-liquids and universal quasi-chemical models and the prediction method univeral quasi-chemical functional activity coefficients were used for generating liquid-liquid equilibrium diagrams for systems made up of acrylic acid, water, and solvents (diisopropyl ether, isopropyl acetate, 2-ethyl hexanol, and methyl isobutyl ketone) and the results were compared with available liquid-liquid equilibrium experimental data. Aspen Plus (Aspen Technology, Inc., version 2004.1) software was used for equilibrium and process calculations. High concentration of acrylic acid was obtained in this article using diisopropyl ether as solvent.

  4. [MORPHOLOGICAL FEATURES OF RAT MUCOUS MEMBRANE OF THE TONGUE EARLY AFFECTED BY ACRYLIC RESIN MONOMER].

    PubMed

    Davydenko, V; Nidzelskiy, M; Starchenko, I; Davydenko, A; Kuznetsov, V

    2016-03-01

    Base materials, made on the basis of various derivatives of acrylic and methacrylic acids, have been widely used in prosthetic dentistry. Free monomer, affecting the tissues of prosthetic bed and the whole body, is always found in dentures. Therefore, study of the effect of acrylic resins' monomer on mucous membrane of the tongue is crucial. Rat tongue is very similar to human tongue, and this fact has become the basis for selecting these animals to be involved into the experiment. The paper presents the findings related to the effect of "Ftoraks" base acrylic resin monomer on the state of rat mucous membrane of the tongue and its regeneration. The microscopy has found that the greatest changes in the mucous membrane of the tongue occur on day 3 and 7 day after applying the monomer and are of erosive and inflammatory nature. Regeneration of tongue epithelium slows down.

  5. Evaluation of liquid-liquid extraction process for separating acrylic acid produced from renewable sugars.

    PubMed

    Alvarez, M E T; Moraes, E B; Machado, A B; Maciel Filho, R; Wolf-Maciel, M R

    2007-04-01

    In this article, the separation and the purification of the acrylic acid produced from renewable sugars were studied using the liquid-liquid extraction process. Nonrandom two-liquids and universal quasi-chemical models and the prediction method universal quasi-chemical functional activity coefficients were used for generating liquid-liquid equilibrium diagrams for systems made up of acrylic acid, water, and solvents (diisopropyl ether, isopropyl acetate, 2-ethyl hexanol, and methyl isobutyl ketone) and the results were compared with available liquid-liquid equilibrium experimental data. Aspen Plus (Aspen Technology, Inc., version 2004.1) software was used for equilibrium and process calculations. High concentration of acrylic acid was obtained in this article using diisopropyl ether as solvent.

  6. Surface modification of cellulosic substrates via atmospheric pressure plasma polymerization of acrylic acid: Structure and properties

    NASA Astrophysics Data System (ADS)

    Garcia-Torres, Jose; Sylla, Dioulde; Molina, Laura; Crespo, Eulalia; Mota, Jordi; Bautista, Llorenç

    2014-06-01

    Surface chemical modification of cellulose-based substrates has been carried out by atmospheric pressure plasma enhanced chemical vapor deposition (AP-PECVD) of acrylic acid. The structure/properties relationship of the samples was studied as a function of the plasma experimental conditions. Acrylic acid monomer/helium ratio and treatment speed clearly influences the wettability properties of the paper substrate: advancing contact angle values were reduced to the half if compare to non-treated paper. Surface morphology of the films did not greatly vary at short polymerization times but fibers were covered by a poly(acrylic acid) film at longer times. FTIR and XPS techniques allowed detecting the retention of carboxylic acid groups/moieties. The possibility to quickly design architectures with tunable carboxylic functions by modifying the plasma processing parameters is shown.

  7. Shade Guide for the Fabrication of Acrylic Denture Based on Mucosal Colour

    PubMed Central

    Da Costa, Godwin Clovis; Aras, Meena Ajay

    2017-01-01

    This article highlights the use of a simple and convenient shade guide system which not only helps in choosing the shade tab that matches with the colour of the mucosa, but, also helps in the fabrication of the precise shade of acrylic resin for making the denture. The shade guide is fabricated by mixing specified quantities of various colours of acrylic polymer in order to obtain various shade tabs. The method for fabrication of the shade guide and the clinical procedure has been discussed. PMID:28384988

  8. Mucin/poly(acrylic acid) interactions: a spectroscopic investigation of mucoadhesion.

    PubMed

    Patel, Minesh M; Smart, John D; Nevell, Thomas G; Ewen, Richard J; Eaton, Peter J; Tsibouklis, John

    2003-01-01

    Studies using infrared, (1)H and (13)C nuclear magnetic resonance, and X-ray photoelectron spectroscopies and differential scanning calorimetry support the hypothesis that hydrogen bonds, formed between the carboxylic acid functionality of the mucoadhesive material poly(acrylic acid) and the glycoprotein component of mucus, play a significant role in the process of mucoadhesion. There are fewer H-bonded interactions between the components than within the bulk of the pure mucoadhesive agent. The pH of the medium influences the structures of both the poly(acrylic acid) and the mucus, which, in turn, determine the nature and the extent of mucoadhesive interactions.

  9. Chemical Fixation of CO{sub 2} to Acrylates Using Low-Valent Molybdenum Sources

    SciTech Connect

    Bernskoetter, Wesley

    2013-09-30

    The kinetic, mechanistic, and reactivity experiments to access the viability and possible reaction design of coupling of carbon dioxide and ethylene at a zerovalent molybdenum for the production of acrylates are described. A general model of the reaction mechanism has been outlined, including assessment of the rate limiting step in the reaction. Kinetic and computational data have valuated the influence of a range of tridentate ligand platforms on the rate of coupling. An in situ reduction and acrylate formation activity screen protocol has also been developed to aid in the technology development of this process. Portions of descriptions of the research products presented here have also been adapted with permission from journal publications.

  10. Enhanced dielectric strength and actuation of acrylic elastomer with silicone gel encapsulation

    NASA Astrophysics Data System (ADS)

    La, Thanh-Giang; Lau, Gih-Keong

    2016-04-01

    Use of dielectric gel encapsulation is reported to make acrylic elastomer (VHB 4905) electrically stronger. Acrylic dielectric elastomer actuators (DEA) with silicone gel encapsulation can sustain an electrical breakdown field of up to 532MV/m, higher than 315MV/m of non-coated ones. Hence, its ultimate areal strain of 228% is larger than 189% of latter. This enhanced dielectric strength and actuation is attributed to the delayed electrothermal breakdown of VHB with silicone gel encapsulant that bars oxygen supply in air.

  11. Laser vibrational overtone activation of ethyl acrylate/benzoyl peroxide mixture

    NASA Astrophysics Data System (ADS)

    Grinevich, Oleg; Snavely, D. L.

    1999-04-01

    Intra- and extracavity laser vibrational overtone polymerization of ethyl acrylate/benzoyl peroxide mixture has been demonstrated. Five photolysis wavenumbers on and near the fifth CH stretch overtone absorption of benzoyl peroxide was investigated. The polymer yield was monitored by observing the decrease in the intensity ratio of the olefinic/methyl and methylenic first CH stretch overtone absorptions of ethyl acrylate. The rate of the polymerization did not depend on the photolysis wavenumber. Molecular weights of the overtone initiated polymers were an order of magnitude larger than those obtained by thermal polymerization. The polymerization rate is compared to the intracavity laser vibrational overtone polymerization of methyl methacrylate.

  12. Inhibiting electro-thermal breakdown of acrylic dielectric elastomer actuators by dielectric gel coating

    NASA Astrophysics Data System (ADS)

    La, Thanh-Giang; Lau, Gih-Keong

    2016-01-01

    Electrical breakdown of dielectric elastomer actuators (DEA) is very localized; a spark and a pinhole (puncture) in dielectric ends up with short-circuit. This letter shows that prevention of electrothermal breakdown helps defer failure of DEAs even with conductive-grease electrodes. Dielectric gel encapsulation or coating (Dow Corning 3-4170) helps protect acrylic elastomer (VHB 4905), making it thermally more stable and delaying its thermal oxidation (burn) from 218 °C to 300 °C. Dielectric-gel-coated acrylic DEAs can withstand higher local leak-induced heating and thus achieve higher dielectric strengths than non-coated DEAs do.

  13. Miconazole activity against Candida biofilms developed on acrylic discs.

    PubMed

    Gebremedhin, S; Dorocka-Bobkowska, B; Prylinski, M; Konopka, K; Duzgunes, N

    2014-08-01

    Oral candidiasis in the form of Candida-associated denture stomatitis (CaDS) is associated with Candida adhesion and biofilm formation on the fitting surface of poly (methyl methacrylate) (PMMA) dentures. Candida biofilms show considerable resistance to most conventional antifungal agents, a phenomenon that is considered a developmental-phase-specific event that may help explain the high recurrence rates associated with CaDS. The aim of this study was to examine the activity of miconazole towards in vitro-grown mature Candida biofilms formed on heat-cured PMMA discs as a standardized model. The effect of miconazole nitrate on Candida biofilms developed on acrylic discs was determined for C. albicans MYA-2732 (ATCC), C. glabrata MYA-275 (ATCC), and clinical isolates, C. albicans 6122/06, C. glabrata 7531/06, C. tropicalis 8122/06, and C. parapsilosis 11375/07. Candida biofilms were developed on heat-cured poly(methyl methacrylate) discs and treated with miconazole (0.5 - 96 μg/ml). The metabolic activity of the biofilms was measured by the XTT reduction assay. The minimum inhibitory concentrations (MICs) of miconazole against Candida species were determined by the microdilution method. The MICs for miconazole for the investigated strains ranged from 0.016-32 μg/ml. Treatment with miconazole resulted in a significant reduction of biofilm metabolic activity for all strains. The highest inhibition was observed at 96 μg/ml miconazole. In the case of C. glabrata MYA-275 and C. tropicalis 8122/06 this corresponded to 83.7% and 75.4% inhibition, respectively. The lowest reduction was observed for C. parapsilosis 11375/07-46.1%. For all Candida strains there was a strong correlation between MIC values and miconazole concentrations corresponding to a reduction of metabolic activity of the biofilm by 50%. Miconazole exhibits high antifungal activity against Candida biofilms developed on the surface of PMMA discs. The study provides support for the use of miconazole as an

  14. 75 FR 770 - Acrylic acid-benzyl methacrylate-1-propanesulfonic acid, 2-methyl-2-[(1-oxo-2-propenyl)amino...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-01-06

    ... AGENCY 40 CFR Part 180 Acrylic acid-benzyl methacrylate-1-propanesulfonic acid, 2- methyl-2... residues of acrylic acid-benzyl methacrylate-1- propanesulfonic acid, 2-methyl-2- -, monosodium salt... to establish a maximum permissible level for residues of acrylic acid-benzyl...

  15. Synthesis and Characterization of Waterborne Fluoropolymers Prepared by the One-Step Semi-Continuous Emulsion Polymerization of Chlorotrifluoroethylene, Vinyl Acetate, Butyl Acrylate, Veova 10 and Acrylic Acid.

    PubMed

    Liu, Hongzhu; Bian, Jiming; Wang, Zhonggang; Hou, Chuan-Jin

    2017-01-22

    Waterborne fluoropolymer emulsions were synthesized using the one-step semi-continuous seed emulsion polymerization of chlorotrifluoroethylene (CTFE), vinyl acetate (VAc), n-butyl acrylate (BA), Veova 10, and acrylic acid (AA). The main physical parameters of the polymer emulsions were tested and analyzed. Characteristics of the polymer films such as thermal stability, glass transition temperature, film-forming properties, and IR spectrum were studied. Meanwhile, the weatherability of fluoride coatings formulated by the waterborne fluoropolymer and other coatings were evaluated by the quick ultraviolet (QUV) accelerated weathering test, and the results showed that the fluoropolymer with more than 12% fluoride content possessed outstanding weather resistance. Moreover, scale-up and industrial-scale experiments of waterborne fluoropolymer emulsions were also performed and investigated.

  16. Tuning the Molar Composition of "Charge-Shifting" Cationic Copolymers Based on 2-(N,N-Dimethylamino)Ethyl Acrylate and 2-(tert-Boc-Amino)Ethyl Acrylate.

    PubMed

    Ho, Hien The; Bohec, Maël Le; Frémaux, Julien; Piogé, Sandie; Casse, Nathalie; Fontaine, Laurent; Pascual, Sagrario

    2017-03-01

    Copolymers of 2-(N,N-dimethylamino)ethyl acrylate (DMAEA) and 2-(tert-Boc-amino)ethyl acrylate (tBocAEA) are synthesized by reversible addition-fragmentation chain transfer polymerization in a controlled manner with defined molar masses and narrow molar masses distributions (Ð ≤ 1.17). Molar compositions of the P(DMAEA-co-tBocAEA) copolymers are assessed by means of (1) H NMR. A complete screening in molar composition is studied from 0% of DMAEA to 100% of DMAEA. Reactivity ratios of both comonomers are determined by the extended Kelen-Tüdos method (r DMAEA = 0.81 and rtBocAEA = 0.99).

  17. Propagation of ultrasonic guided waves in an acrylic plate as a cortical-bone-mimicking phantom

    NASA Astrophysics Data System (ADS)

    Lee, Kang Il; Choi, Bok Kyoung

    2014-12-01

    The present study aims to investigate the propagation of ultrasonic guided waves in an acrylic plate as a cortical-bone-mimicking phantom. The velocities of the guided waves in a 5-mm-thick acrylic plate were measured by using the axial transmission technique. A pure A0 Lamb mode could be successfully launched in the 5-mm-thick acrylic plate through a time reversal process of Lamb waves, consistent with the fact that the time reversal process can automatically compensate for the dispersive nature of Lamb waves. The experimental velocities of the slow guided wave (SGW) and the time-reversed Lamb wave were found to be in reasonable agreement with the theoretical group velocity of the A0 Lamb mode, suggesting that both the SGW and the time-reversed Lamb wave excited in the 5-mm-thick acrylic plate correspond to the A0 Lamb mode. These results suggest that the time reversal process of Lamb waves can be usefully applied to noninvasive characterization of long cortical bones.

  18. Synthesis and characterization of poly(sodium acrylate)/ bentonite superabsorbent composite

    NASA Astrophysics Data System (ADS)

    Xie, Yiming; Wei, Yuelin; Huang, Yunfang; Lin, Jianming; Wu, Jihuai

    2012-01-01

    Poly(sodium acrylate)/bentonite superabsorbent composite with water absorbency 1562 g·g-1 was synthesized by inverse suspension polymerization. The introduction of bentonite improves the water absorbency and facilitates the particle size even distribution of the composite. The network structure in the superabsorbent hydrogel is confirmed.

  19. Copper-acrylic enamel serves as lubricant for cold drawing of refractory metals

    NASA Technical Reports Server (NTRS)

    Beane, C.; Karasek, F.

    1966-01-01

    Acrylic enamel spray containing metallic copper pigment lubricates refractory metal tubing during cold drawing operations so that the tubing surface remains free from scratches and nicks and does not seize in the die. Zirconium alloys, zirconium, tantalum alloys, niobium alloys, vanandium alloys and titanium alloys have been drawn using this lubricant.

  20. Do flexible acrylic resin lingual flanges improve retention of mandibular complete dentures?

    PubMed Central

    Ahmed Elmorsy, Ayman Elmorsy; Ahmed Ibraheem, Eman Mostafa; Ela, Alaa Aboul; Fahmy, Ahmed; Nassani, Mohammad Zakaria

    2015-01-01

    Objectives: The aim of this study was to compare the retention of conventional mandibular complete dentures with that of mandibular complete dentures having lingual flanges constructed with flexible acrylic resin “Versacryl.” Materials and Methods: The study sample comprised 10 completely edentulous patients. Each patient received one maxillary complete denture and two mandibular complete dentures. One mandibular denture was made of conventional heat-cured acrylic resin and the other had its lingual flanges made of flexible acrylic resin Versacryl. Digital force-meter was used to measure retention of mandibular dentures at delivery and at 2 weeks and 45 days following denture insertion. Results: The statistical analysis showed that at baseline and follow-up appointments, retention of mandibular complete dentures with flexible lingual flanges was significantly greater than retention of conventional mandibular dentures (P < 0.05). In both types of mandibular dentures, retention of dentures increased significantly over the follow-up period (P < 0.05). Conclusions: The use of flexible acrylic resin lingual flanges in the construction of mandibular complete dentures improved denture retention. PMID:26539387

  1. 40 CFR 721.10192 - Amides, coco, N-[3-(dibutylamino)propyl], acrylates.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Amides, coco, N- , acrylates. 721.10192 Section 721.10192 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10192 Amides, coco, N-...

  2. Influencing Solvent Miscibility and Aqueous Stability of Aluminum Nanoparticles through Surface Functionalization with Acrylic Monomers (Postprint)

    DTIC Science & Technology

    2010-08-26

    Methacryloxypropyltrimethoxysilane (MPS), 2-carboxyethyl acrylate (CEA), phosphoric acid 2-hy- droxyethyl methacrylate ester (PAM), methyl methacrylate (MMA), cyclohexanone ...0.070 g, 0.43 mmol) was dissolved in dry cyclohexanone (25 mL) and added to the reaction vessel via the use of a cannula. The vessel was then immersed

  3. Computational Study of the Self-Initiation Mechanism in Thermal Polymerization of Methyl Acrylate

    NASA Astrophysics Data System (ADS)

    Srinivasan, Sriraj; Lee, Myung Won; Grady, Michael C.; Soroush, Masoud; Rappe, Andrew M.

    2009-09-01

    This computational study deals with the mechanism of spontaneous initiation in thermal polymerization of alkyl acrylates (e.g., methyl, ethyl, and n-butyl acrylate). The mechanism is presently still unknown. Density-functional theory (DFT) and Møller-Plesset (MP2) calculations are used to explore the Flory and Mayo mechanisms of self-initiation in methyl acrylate. On the singlet surface, a low-barrier, concerted [4 + 2] Diels-Alder mechanism for the formation of a dihydropyran adduct (DA) and a high-barrier nonconcerted [2 + 2] diradical (•M2s•) mechanism for the formation of dimethyl cyclobutane-1,2-dicarboxylate (DCD) were found using B3LYP/6-31G*. Several levels of theory were used to validate the transition states, and the pathways for the DA and DCD formations on the singlet surface were determined using intrinsic reaction coordinate (IRC) calculations. On the triplet surface, a triplet diradical intermediate (•M2t•) was identified that is structurally similar to •M2s• but lower in energy. The spin-orbit coupling constant for crossover of the diradical from singlet to triplet surface was calculated. Monoradical generation from the two intermediates, DA and •M2t• via hydrogen transfer to or from a third methyl acrylate was studied. It was found that generation of two monoradical species was possible from •M2t• and is proposed as a likely explanation for experimentally observed spontaneous-initiation.

  4. Synthesis and antibacterial properties of beta-diketone acrylate bioisosteres of pseudomonic acid A.

    PubMed

    Bennett, I; Broom, N J; Cassels, R; Elder, J S; Masson, N D; O'Hanlon, P J

    1999-07-05

    A series of beta-diketone acrylate bioisosteres 4 of pseudomonic acid A 1 have been synthesized and evaluated for their ability to inhibit bacterial isoleucyl-tRNA synthetase and act as antibacterial agents. A number of analogues have excellent antibacterial activity. Selected examples were shown to afford good blood levels and to be effective in a murine infection model.

  5. 40 CFR 721.10339 - Adipic acid, substituted propane, alkyldiol, acrylate (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Adipic acid, substituted propane... Significant New Uses for Specific Chemical Substances § 721.10339 Adipic acid, substituted propane, alkyldiol... substance identified generically as adipic acid, substituted propane, alkyldiol, acrylate (PMN P-04-113)...

  6. 40 CFR 721.10339 - Adipic acid, substituted propane, alkyldiol, acrylate (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Adipic acid, substituted propane... Significant New Uses for Specific Chemical Substances § 721.10339 Adipic acid, substituted propane, alkyldiol... substance identified generically as adipic acid, substituted propane, alkyldiol, acrylate (PMN P-04-113)...

  7. 40 CFR 721.10339 - Adipic acid, substituted propane, alkyldiol, acrylate (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Adipic acid, substituted propane... Significant New Uses for Specific Chemical Substances § 721.10339 Adipic acid, substituted propane, alkyldiol... substance identified generically as adipic acid, substituted propane, alkyldiol, acrylate (PMN P-04-113)...

  8. Structure-function properties of starch spherulites grafted with poly(methyl acrylate)

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Spherulites, produced by steam jet-cooking high-amylose starch and oleic acid, were grafted with methyl acrylate, both before and after removal of un-complexed amylopectin. For comparison, granular high-amylose corn starch was graft polymerized in a similar manner. The amount of grafted and ungrafte...

  9. Structure-function properties of starch graft poly(methyl acrylate)copolymers

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Spherulites, produced by steam jet-cooking high-amylose starch and oleic acid, were grafted with methyl acrylate, both before and after removal of un-complexed amylopectin. For comparison, granular high-amylose corn starch was graft polymerized in a similar manner. The amount of grafted and ungrafte...

  10. The Influence of Chicken Egg Shell as Fillers on Biocomposite Acrylic Resin for Denture Based

    NASA Astrophysics Data System (ADS)

    Lubis, M.; Ginting, M. H. S.; Dalimunthe, N. F.; Hasibuan, D. M. T.; Sastrodihardjo, S.

    2017-03-01

    This research was conducted to discover the influence of the addition of chicken egg shells microparticle as filler on the mechanical properties such as modulus of elasticity, modulus of rapture and particle size analysis on biocomposite acrylic resin for denture based. The raw materials used in this research were acrylic resin, egg shell, cold mold seals, gypsum, Vaseline and wax. The process of making biocomposite acrylic resin for denture based with mix the acrylic resin in ratio 2:1 (w/w). Then added the microparticle filler 0,10,20,30 (%w) to mold and boil in 75°C for 90 minutes and increase the temperature to 90 °C for 30 minutes. Took the sample and let it dried. The results of research showed the increase of modulus elasticity and modulus of rapture. The modulus of elasticity showed a very significant increase by adding fillers 10% of 2.123 GPa, which was only 1.932 GPa without adding the filler of chicken egg shells. For modulus of rapture showed the increase by adding fillers 20% of 48,311MPa, which was only 46,865 GPa without adding the filler of chicken egg shells

  11. Possible utilization of acrylic paint and copper phthalocyanine pigment sludge for vermiculture.

    PubMed

    Majumdar, Deepanjan; Buch, Vaidehi; Macwan, Praisy; Patel, Jignesh

    2010-05-01

    Sludge generated from water treatment plants in two different paint and pigment manufacturing industries, one manufacturing CPC Green (copper phthalocyanine green) and the other acrylic (pure and styrene) washable distempers, synthetic enamels, fillers and putties, were used for culturing earthworms (Eisenia foetida Savigny). The possibility of getting a quality vermicompost was also explored. The sludges were used pure and mixed with month-old cow dung at 1:1, 1:2, 1:3, 2:1 and 3:1 ratios (sludge:cow dung). In pure sludges and in the 3:1 ratio, earthworms did not survive. Earthworms had very low survival in CPC Green sludge and its mixtures while acrylic paint sludge was very efficient in supporting worm growth and worm castings were generated quickly. Both sludges were alkaline, non-saline, but had appreciable Ca, Al, Pb, Zn, and Mn. CPC Green had high Cu (12,900 mg kg(-1)) and acrylic paint sludge had high total Cr (155 mg kg(-1)). High Ca and Al in both came from water treatment chemicals (lime and alum), while CPC Green itself is a copper-based pigment. The sludges were suitable for land application with regard to their metal contents, except for Cu in CPC Green. CPC Green did not support proper growth of plants (green gram, Vigna radiata (L). R. Wilcz.), while acrylic paint sludge supported growth in pure form and mixtures with soil.

  12. Cytotoxic effects of acrylates and methacrylates: relationships of monomer structures and cytotoxicity.

    PubMed

    Yoshii, E

    1997-12-15

    Thirty-nine acrylates and methacrylates that had been used in dental resin materials were evaluated by a cytotoxicity test, and the relationships between their structures and cytotoxicity were studied to predict cytotoxic levels of dental resin materials in order to develop new low-toxic resin materials. All the acrylates evaluated were more toxic than corresponding methacrylates. In both the acrylates and methacrylates, a hydroxyl group seemed to enhance cytotoxicity. Dimethacrylates with 14 or fewer oxyethylene chains showed similar cytotoxicity while dimethacrylates with 23 oxyethylene chains showed lower cytotoxicity. The cytotoxicity ranking of monomers widely used in dental resin materials was bisphenol A bis 2-hydroxypropyl methacrylate (bisGMA) > urethane dimethacrylate (UDMA) > triethyleneglycol dimethacrylate (3G) > 2-hydroxyethyl methacrylate (HEMA) > methyl methacrylate (MMA). In acrylates, methacrylates, and ethylmethacrylates with either substituents, the lipophilicity of substituents affected their cytotoxicity, and an inverse correlation between IC50 and logP was observed. These results will be useful in developing new resin materials with low toxic monomer compositions.

  13. Swelling, diffusion, network parameters and adsorption properties of IPN hydrogel of chitosan and acrylic copolymer.

    PubMed

    Mandal, Bidyadhar; Ray, Samit Kumar

    2014-11-01

    Interpenetrating network (IPN) type hydrogels of a biopolymer and a synthetic polymer were prepared from chitosan and crosslink copolymer of acrylic acid, sodium acrylate and hydroxyethyl methacrylate. Acrylic acid, sodium acrylate, hydroxyethyl methacrylate and N'N'-methylenebisacrylamide (MBA) monomers were free radically copolymerized and crosslinked in aqueous solution of chitosan. Several IPN hydrogels were prepared by varying concentrations of initiator, crosslinker (MBA) and weight% of chitosan . These hydrogels were characterized by free acid content, pH at point of zero charge (PZC), FTIR, DTA-TGA, SEM and XRD. The swelling and diffusion characteristics, network parameters and adsorption of cationic methyl violet (MV) and anionic congo red (CR) dyes by these hydrogels were studied. The hydrogels showed high adsorption (9.5-119 mg/g for CR and 9.2-98 mg/g for MV) and removal% (98-73% for CR and 94-66% for MV) over the feed concentration of 10-140 mg/l dye in water. The isotherms and kinetics of dye adsorption by the hydrogels were also studied.

  14. Stable emulsion copolymers of acrylamide and ammonium acrylate for use in enhanced oil recovery

    SciTech Connect

    Frank, S.; Coscia, A.T.; Schmitt, J.M.

    1984-03-27

    There is provided a process for recovering oil from oil bearing formations employing the use of a water treating medium, which medium comprises the inclusion of a novel stable emulsion copolymer of acrylamide and ammonium acrylate as well as the emulsion copolymer per se.

  15. 40 CFR 721.10389 - Styrene, copolymer with acrylic acid, salt with alkoxylated alkenylamine (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10389 Styrene, copolymer with acrylic acid, salt with alkoxylated alkenylamine (generic). (a) Chemical substance and significant new...

  16. 40 CFR 721.10389 - Styrene, copolymer with acrylic acid, salt with alkoxylated alkenylamine (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10389 Styrene, copolymer with acrylic acid, salt with alkoxylated alkenylamine (generic). (a) Chemical substance and significant new...

  17. Assessment of the flexural strength of two heat-curing acrylic resins for artificial eyes.

    PubMed

    Fernandes, Aline Ursula Rocha; Portugal, Aline; Veloso, Letícia Rocha; Goiato, Marcelo Coelho; Santos, Daniela Micheline dos

    2009-01-01

    Prosthetic eyes are artificial substitutes for the eyeball, made of heat-curing acrylic resin, serving to improve the esthetic appearance of the mutilated patient and his/her inclusion in society. The aim of this study was to assess the flexural strength of two heat-curing acrylic resins used for manufacturing prosthetic eyes. Thirty-six specimens measuring 64 x 10 x 3.3 mm were obtained and divided into four groups: acrylic resin for artificial sclera N1 (Artigos Odontológicos Clássico, São Paulo, SP, Brazil), heat-cure water technique (GI) and microwave-cured (GII); colorless acrylic resin for prosthetic eyes (Artigos Odontológicos Clássico, São Paulo, SP, Brazil), heat-cure water technique (GIII) and microwave-cured (GIV). Mechanical tests using three point loads were performed in a test machine (EMIC, São José dos Pinhais, PR, Brazil). The analysis of variance and the Tukey test were used to identify significant differences (p < 0.01). Groups GII and GIV presented, respectively, the highest (98.70 +/- 11.90 MPa) and lowest means (71.07 +/- 8.93 MPa), with a statistically significant difference. The cure method used for the prosthetic eye resins did not interfere in their flexural strength. It was concluded that all the resins assessed presented sufficient flexural strength values to be recommended for the manufacture of prosthetic eyes.

  18. 40 CFR 721.338 - Salt of an acrylate copolymer (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.338 Salt of an acrylate copolymer (generic). Link to an amendment published at 79 FR 34636, June 18, 2014. (a) Chemical substance and significant new uses subject to reporting. (1) The...

  19. Transcatheter Embolization of a Large Symptomatic Pelvic Arteriovenous Malformation with Glubran 2 Acrylic Glue

    SciTech Connect

    Gandini, R.; Angelopoulos, G. Konda, D.; Messina, M.; Chiocchi, M.; Perretta, T.; Simonetti, G.

    2008-09-15

    A young patient affected by a pelvic arteriovenous malformation (pAVM) with recurrent episodes of hematuria following exercise, underwent transcatheter embolization using Glubran 2 acrylic glue (GEM, Viareggio, Italy). All branches of the pAVM were successfully occluded. The patient showed prompt resolution of symptoms and persistent occlusion of the pAVM at the 6 month follow-up.

  20. Prosthodontic self-treatment with acrylic resin super glue: a case report.

    PubMed

    Winkler, Sheldon; Wood, Robert; Facchiano, Anne M; Boberick, Kenneth G; Patel, Amita R

    2006-01-01

    A case history is presented of a patient who fabricated 3 prostheses from autopolymerizing acrylic resin intended for fingernail augmentation and then cemented them into her mouth with super glue. Patients must be warned not to attempt self-treatment for esthetics with self-fabricated prostheses because severe adverse and irreversible hard and soft tissue reactions may occur.

  1. Morphological alteration of microwave disinfected acrylic resins used for dental prostheses

    NASA Astrophysics Data System (ADS)

    Popescu, M. C.; Bita, B. I.; Avram, A. M.; Tucureanu, V.; Schiopu, P.

    2015-02-01

    In this paper we aim to perform a cross section morphological characterization of an acrylic polymer used for dental prostheses subjected to microwave disinfection. The method was largely investigated and the microbiological effectiveness is well established, but there are some issues regarding the in-depth alteration of the material. In our research, the surface roughness is insignificant and the samples were not polished or refined by any means. Two groups of 7 acrylic discs (20 mm diameter, 2 mm thickness) were prepared from a heat-cured powder. Half of the samples embedded a stainless steel reinforcement, in order to observe the changes at the interfaces between the polymer and metallic wire. After the gradual wet microwave treatment, the specimens - including the controls - were frozen in liquid nitrogen and broken into pieces. Fragments were selected for gold metallization to ensure a good contrast for SEM imaging. We examined the samples in cross section employing a high resolution SEM. We have observed the alterations occurred at the surface of the acrylic sample and at the interface with the metallic wire along with the increase of the power and exposure time. The bond configuration of acrylate samples was analysed by FTIR spectrometry.

  2. 76 FR 77709 - Butyl acrylate-methacrylic acid-styrene polymer; Tolerance Exemption

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-14

    ... AGENCY 40 CFR Part 180 Butyl acrylate-methacrylic acid-styrene polymer; Tolerance Exemption AGENCY... from the requirement of a tolerance for residues of 2-Propenoic acid, 2-methyl-, polymer with butyl 2...-styrene polymer when used as an inert ingredient in a pesticide chemical formulation....

  3. 21 CFR 177.2000 - Vinylidene chloride/methyl acrylate/methyl methacrylate polymers.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... methacrylate polymers. 177.2000 Section 177.2000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic.../methyl methacrylate polymers. The vinylidene chloride/methyl acrylate/methyl methacrylate polymers...

  4. 21 CFR 177.2000 - Vinylidene chloride/methyl acrylate/methyl methacrylate polymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... methacrylate polymers. 177.2000 Section 177.2000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF...: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.2000 Vinylidene chloride/methyl acrylate/methyl methacrylate polymers. The vinylidene chloride/methyl...

  5. 21 CFR 177.2000 - Vinylidene chloride/methyl acrylate/methyl methacrylate polymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... methacrylate polymers. 177.2000 Section 177.2000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF...: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.2000 Vinylidene chloride/methyl acrylate/methyl methacrylate polymers. The vinylidene chloride/methyl...

  6. 21 CFR 177.2000 - Vinylidene chloride/methyl acrylate/methyl methacrylate polymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... methacrylate polymers. 177.2000 Section 177.2000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF...: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.2000 Vinylidene chloride/methyl acrylate/methyl methacrylate polymers. The vinylidene chloride/methyl...

  7. 21 CFR 177.2000 - Vinylidene chloride/methyl acrylate/methyl methacrylate polymers.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... methacrylate polymers. 177.2000 Section 177.2000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF...: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.2000 Vinylidene chloride/methyl acrylate/methyl methacrylate polymers. The vinylidene chloride/methyl...

  8. Effect of Nanoclay on Thermal Conductivity and Flexural Strength of Polymethyl Methacrylate Acrylic Resin

    PubMed Central

    Ghaffari, Tahereh; Barzegar, Ali; Hamedi Rad, Fahimeh; Moslehifard, Elnaz

    2016-01-01

    Statement of the Problem The mechanical and thermal properties of polymethyl methacrylate (PMMA) acrylic resin should be improved to counterweigh its structural deficiencies. Purpose The aim of this study was to compare the flexural strength and thermal conductivity of conventional acrylic resin and acrylic resin loaded with nanoclay. Materials and Method The methacrylate monomer containing the 0.5, 1 and 2 wt% of nanoclay was placed in an ultrasonic probe and mixed with the PMMA powder. Scanning electron microscopy was used to verify homogeneous distribution of particles. Twenty-four 20×20×200-mm cubic samples were prepared for flexural strength test; 18 samples containing nanoclay and 6 samples for the control group. Another 24 cylindrical samples of 38×25 mm were prepared for thermal conductivity test. One-way ANOVA was used for statistical analysis, followed by multiple-comparison test (Scheffé’s test). Statistical significance was set at p< 0.05. Results Increasing the concentration of nanoclay incorporated into the acrylic resin samples increased thermal conductivity but decreased flexural strength (p< 0.05). Conclusion Based on the results of this study, adding nanoclay particles to PMMA improved its thermal conductivity, while it had a negative effect on the flexural strength. PMID:27284557

  9. Bond Strength of Repaired Acrylic Denture Teeth Using Visible Light Cure Composite Resin

    PubMed Central

    Muhsin, Saja Ali

    2017-01-01

    Background: Although bonding to denture teeth after surface treatment with chemical agents is desirable, there is little information on the use of Visible Light Cure composite resin (VLC) as bonding denture materials. Objectives: To determine the effect of various surface treatments on shear bond strength between Visible Light Cure composite resin and the acrylic denture teeth interface. Methods: Forty cylindrical sticks of acrylic resin with denture teeth mounted atop were prepared. Various treatments were implemented upon the acrylic resin teeth surfaces. The samples were divided into four groups (n = 10). Light-cured composite resin (LC) was applied over all treated and untreated surfaces of tested groups. The shear bond was tested using a universal tensile testing apparatus with the knife-edge of a 0.8mm shear tester. Data were statistically analyzed using one-way ANOVA performed at a confidence level of 95% and significant P-value of (P ≤ 0.05). Results: Analysis of variance (ANOVA) showed statistically significant difference (P < 0.05) between treated and untreated teeth surfaces. The treated surfaces exhibited various levels of bond strength depending on the type of treatment. Conclusion: Application of VLC bonding agent with prior treatment of methylmethacrylate (MMA) on the acrylic resin denture teeth resulted in maximum bond strength with composite resin.

  10. Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer

    PubMed Central

    Lee, Kyung Dong; Jeong, Young-Il; Kim, Da Hye; Lim, Gyun-Taek; Choi, Ki-Choon

    2013-01-01

    Background Although cisplatin is extensively used in the clinical field, its intrinsic toxicity limits its clinical use. We investigated nanoparticle formations of poly(acrylic acid-co-methyl methacrylate) (PAA-MMA) incorporating cisplatin and their antitumor activity in vitro and in vivo. Methods Cisplatin-incorporated nanoparticles were prepared through the ion-complex formation between acrylic acid and cisplatin. The anticancer activity of cisplatin-incorporated nanoparticles was assessed with CT26 colorectal carcinoma cells. Results Cisplatin-incorporated nanoparticles have small particle sizes of less than 200 nm with spherical shapes. Drug content was increased according to the increase of the feeding amount of cisplatin and acrylic acid content in the copolymer. The higher acrylic acid content in the copolymer induced increase of particle size and decrease of zeta potential. Cisplatin-incorporated nanoparticles showed a similar growth-inhibitory effect against CT26 tumor cells in vitro. However, cisplatin-incorporated nanoparticles showed improved antitumor activity against an animal tumor xenograft model. Conclusion We suggest that PAA-MMA nanoparticles incorporating cisplatin are promising carriers for an antitumor drug-delivery system. PMID:23966778

  11. Transdermal thiol-acrylate polyethylene glycol hydrogel synthesis using near infrared light

    NASA Astrophysics Data System (ADS)

    Chung, Solchan; Lee, Hwangjae; Kim, Hyung-Seok; Kim, Min-Gon; Lee, Luke P.; Lee, Jae Young

    2016-07-01

    Light-induced polymerization has been widely applied for hydrogel synthesis, which conventionally involves the use of ultraviolet or visible light to activate a photoinitiator for polymerization. However, with these light sources, transdermal gelation is not efficient and feasible due to their substantial interactions with biological systems, and thus a high power is required. In this study, we used biocompatible and tissue-penetrating near infrared (NIR) light to remotely trigger a thiol-acrylate reaction for efficient in vivo gelation with good controllability. Our gelation system includes gold nanorods as a photothermal agent, a thermal initiator, diacrylate polyethylene glycol (PEG), and thiolated PEG. Irradiation with a low-power NIR laser (0.3 W cm-2) could induce gelation via a mixed-mode reaction with a small increase in temperature (~5 °C) under the optimized conditions. We also achieved successful transdermal gelation via the NIR-assisted photothermal thiol-acryl reactions. This new type of NIR-assisted thiol-acrylate polymerization provides new opportunities for in situ hydrogel formation for injectable hydrogels and delivery of drugs/cells for various biomedical applications.Light-induced polymerization has been widely applied for hydrogel synthesis, which conventionally involves the use of ultraviolet or visible light to activate a photoinitiator for polymerization. However, with these light sources, transdermal gelation is not efficient and feasible due to their substantial interactions with biological systems, and thus a high power is required. In this study, we used biocompatible and tissue-penetrating near infrared (NIR) light to remotely trigger a thiol-acrylate reaction for efficient in vivo gelation with good controllability. Our gelation system includes gold nanorods as a photothermal agent, a thermal initiator, diacrylate polyethylene glycol (PEG), and thiolated PEG. Irradiation with a low-power NIR laser (0.3 W cm-2) could induce gelation

  12. Data of continuous harvest of stem cells via partial detachment from thermoresponsive nanobrush surfaces

    PubMed Central

    Yeh, Chin-Chen; Muduli, Saradaprasan; Peng, I-Chia; Lu, Yi-Tung; Ling, Qing-Dong; Alarfaj, Abdullah A.; Munusamy, Murugan A.; Kumar, S. Suresh; Murugan, Kadarkarai; Chen, Da-Chung; Lee, Hsin-chung; Chang, Yung; Higuchi, Akon

    2016-01-01

    This data article contains two figures and one table supporting the research article entitled: “Continuous harvest of stem cells via partial detachment from thermoresponsive nanobrush surface” [1]. The table shows coating conditions of three copolymers, poly(styrene-co-acrylic acid) grafted with oligovitronectin, poly(styrene-co-N-isopropylacrylamide) and poly(styrene-co-polyethylene glycol methacrylate) to prepare thermoresponsive surface. XPS spectra show the nitrogen peak of the polystyrene surface coated with poly(styrene-co-acrylic acid) grafted with oligovitronectin. The surface coating density analyzed from sorption of poly(styrene-co-acrylic acid) grafted with oligovitronectin by UV–vis spectroscopy is also presented. PMID:26909373

  13. Data of continuous harvest of stem cells via partial detachment from thermoresponsive nanobrush surfaces.

    PubMed

    Yeh, Chin-Chen; Muduli, Saradaprasan; Peng, I-Chia; Lu, Yi-Tung; Ling, Qing-Dong; Alarfaj, Abdullah A; Munusamy, Murugan A; Kumar, S Suresh; Murugan, Kadarkarai; Chen, Da-Chung; Lee, Hsin-Chung; Chang, Yung; Higuchi, Akon

    2016-03-01

    This data article contains two figures and one table supporting the research article entitled: "Continuous harvest of stem cells via partial detachment from thermoresponsive nanobrush surface" [1]. The table shows coating conditions of three copolymers, poly(styrene-co-acrylic acid) grafted with oligovitronectin, poly(styrene-co-N-isopropylacrylamide) and poly(styrene-co-polyethylene glycol methacrylate) to prepare thermoresponsive surface. XPS spectra show the nitrogen peak of the polystyrene surface coated with poly(styrene-co-acrylic acid) grafted with oligovitronectin. The surface coating density analyzed from sorption of poly(styrene-co-acrylic acid) grafted with oligovitronectin by UV-vis spectroscopy is also presented.

  14. The effect of flexible acrylic resin on masticatory muscle activity in implant-supported mandibular overdentures: a controlled clinical trial

    PubMed Central

    Ibraheem, Eman Mostafa Ahmed; Nassani, Mohammad Zakaria

    2016-01-01

    Background It is not yet clear from the current literature to what extent masticatory muscle activity is affected by the use of flexible acrylic resin in the construction of implant-supported mandibular overdentures. Objective To compare masticatory muscle activity between patients who were provided with implant-supported mandibular overdentures constructed from flexible acrylic resin and those who were provided with implant-supported mandibular overdentures constructed from heat-cured conventional acrylic resin. Methods In this clinical trial, 12 completely edentulous patients were selected and randomly allocated into two equal treatment groups. Each patient in Group 1 received two implants to support a mandibular overdenture made of conventional acrylic resin. In Group 2, the patients received two implants to support mandibular overdentures constructed from “Versacryl” flexible acrylic resin. The maxillary edentulous arch for patients in both groups was restored by conventional complete dentures. For all patients, masseter and temporalis muscle activity was evaluated using surface electromyography (sEMG). Results The results showed a significant decrease in masticatory muscle activity among patients with implant-supported mandibular overdentures constructed from flexible acrylic resin. Conclusion The use of “Versacryl” flexible acrylic resin in the construction of implant-supported mandibular overdentures resulted in decreased masticatory muscle activity. PMID:26955445

  15. Multi-functional hybrid coatings containing silica nanoparticles and anti-corrosive acrylate monomer for scratch and corrosion resistance.

    PubMed

    Seo, Ji Yeon; Han, Mijeong

    2011-01-14

    Multi-functional hybrid coatings having both anti-corrosion and scratch resistance were prepared from modified silica nanoparticles and functional acrylates. To improve the dispersion properties of silica nanoparticles in the organic/inorganic hybrid coatings, the surface of the nanoparticles was modified with γ-methacryloxypropyltrimethoxysilane. The coating solution could be prepared by mixing modified silica nanoparticles, tetrasiloxane acrylate, di-acrylate monomer containing an anti-corrosion functional group, acrylic acid, and an initiator in a solvent. The mixture was then dip-coated on iron substrates and finally polymerized by ultraviolet (UV) irradiation. Corrosion and scratch resistance of the coated iron was evaluated by electrochemical impedance spectroscopy (EIS) and a pencil hardness test, respectively. From the EIS results, the coatings with tetrasiloxane acrylate and di-acrylate did not show any decrease in impedance or phase angle, even after 50 days' exposure to 0.1 M NaCl electrolyte, whereas the conventional acrylate coatings started to fail after only 24 h. A hybrid coating containing the amine-quinone functional group exhibited excellent corrosion protection properties with 4-5H pencil hardness.

  16. Self-initiation of UV photopolymerization reactions using tetrahalogenated bisphenol A (meth)acrylates.

    PubMed

    Pelras, Théophile; Knolle, Wolfgang; Naumov, Sergej; Heymann, Katja; Daikos, Olesya; Scherzer, Tom

    2017-02-17

    The potential of tetrachlorinated and tetrabrominated bisphenol A diacrylates and dimethacrylates for self-initiation of a radical photopolymerization was investigated. The kinetics of the photopolymerization of an acrylic model varnish containing halogenated monomers was studied by real-time FTIR spectroscopy, whereas the formation of reactive species and secondary products was elucidated by laser flash photolysis and product analysis by GC-MS after steady-state photolysis. The interpretation of the experimental data and the analysis of possible reaction pathways were assisted by quantum chemical calculations. It was shown that all halogenated monomers lead to a significant acceleration of the photopolymerization kinetics at a minimum concentration of 5 wt%. Steady-state and laser flash photolysis measurements as well as quantum chemical calculations showed that brominated and chlorinated samples do not follow the same pathway to generate radical species. Whereas chlorinated (meth)acrylates may cleave only at the C-O bonds of the carboxyl groups resulting in acrolein and oxyl radicals for initiation, brominated monomers may cleave either at the C-O bonds or at the C-Br bonds delivering aryl and bromine radicals. The quantum yields for the photolysis of the halogenated monomers were found to be in the order of 0.1 for acrylates and 0.2 for methacrylates (with an estimated error of 25%), independently of the attached Br and Cl halogens. Finally, the trihalogenated bisphenol A di(meth)acrylate radicals and the acrolein radicals were found to show the highest efficiencies for the reaction with another acrylic double bond leading to the formation of a polymer network.

  17. Influence of ozone and paracetic acid disinfection on adhesion of resilient liners to acrylic resin

    PubMed Central

    2016-01-01

    PURPOSE The aim of this study was to evaluate the effect of paracetic acid (PAA) and ozone disinfection on the tensile bond strength (TBS) of silicone-based resilient liners to acrylic resins. MATERIALS AND METHODS One hundred and twenty dumbbell shaped heat-polymerized acrylic resins were prepared. From the mid segment of the specimens, 3 mm of acrylic were grinded off and separated parts were reattached by resilient liners. The specimens were divided into 2 control (control1, control7) and 4 test groups of PAA and ozone disinfection (PAA1, PAA7, ozone1 and ozone7; n=10). While control groups were immersed in distilled water for 10 min (control1) and 7 days (control7), test groups were subjected to PAA (16 g/L) or ozone rich water (4 mg/L) for 1 cycle (10 min for PAA and 60 min for ozone) per day for 7 days prior to tensile tests. Measurements of the TBS were analyzed using 3-way ANOVA and Tukey's HSD test. RESULTS Adhesive strength of Mollosil decreased significantly by application of ozone disinfection. PAA disinfection had no negative effect on the TBS values of Mollosil and Molloplast B to acrylic resin. Single application of ozone disinfection did not have any negative effect on TBS values of Molloplast B, but prolonged exposure to ozone decreased its adhesive strength. CONCLUSION The adhesion of resilient liners to acrylic was not adversely affected by PAA disinfection. Immersion in ozonated water significantly decreased TBS of Mollosil. Prolonged exposure to ozone negatively affects adhesion of Molloplast B to denture base materials. PMID:27555898

  18. Effect of tyrosol on adhesion of Candida albicans and Candida glabrata to acrylic surfaces.

    PubMed

    Monteiro, Douglas Roberto; Feresin, Leonardo Perina; Arias, Laís Salomão; Barão, Valentim Adelino Ricardo; Barbosa, Debora Barros; Delbem, Alberto Carlos Botazzo

    2015-09-01

    The prevention of adhesion of Candida cells to acrylic surfaces can be regarded as an alternative to prevent denture stomatitis. The use of quorum sensing molecules, such as tyrosol, could potentially interfere with the adhesion process. Therefore, the aim of this study was to assess the effect of tyrosol on adhesion of single and mixed cultures of Candida albicans and Candida glabrata to acrylic resin surfaces. Tyrosol was diluted in each yeast inoculum (10(7) cells/ml in artificial saliva) at 25, 50, 100, and 200 mM. Then, each dilution was added to wells of 24-well plates containing the acrylic specimens, and the plates were incubated at 37°C for 2 h. After, the effect of tyrosol was determined by total biomass quantification, metabolic activity of the cells and colony-forming unit counting. Chlorhexidine gluconate (CHG) was used as a positive control. Data were analyzed using analysis of variance (ANOVA) and the Holm-Sidak post hoc test (α = 0.05). The results of total biomass quantification and metabolic activity revealed that the tyrosol promoted significant reductions (ranging from 22.32 to 86.16%) on single C. albicans and mixed cultures. Moreover, tyrosol at 200 mM and CHG significantly reduced (p < 0.05) the number of adhered cells to the acrylic surface for single and mixed cultures of both species, with reductions ranging from 1.74 to 3.64-log10. In conclusion, tyrosol has an inhibitory effect on Candida adhesion to acrylic resin, and further investigations are warranted to clarify its potential against Candida infections.

  19. Pre-irradiation induced emulsion co-graft polymerization of acrylonitrile and acrylic acid onto a polyethylene nonwoven fabric

    NASA Astrophysics Data System (ADS)

    Liu, Hanzhou; Yu, Ming; Ma, Hongjuan; Wang, Ziqiang; Li, Linfan; Li, Jingye

    2014-01-01

    A pre-irradiation induced emulsion co-graft polymerization method was used to introduce acrylonitrile and acrylic acid onto a PE nonwoven fabric. The use of acrylic acid is meant to improve the hydrophilicity of the modified fabric. The kinetics of co-graft polymerization were studied. The existence of polyacrylonitrile (PAN) and poly(acrylic acid) (PAAc) graft chains was proven by Fourier transform infrared spectroscopy (FTIR) analysis. The existence of the nitrile groups in the graft chains indicates that they are ready for further amidoximation and adsorption of heavy metal ions.

  20. Development of a novel oxirane-acrylate composite restorative resin material

    NASA Astrophysics Data System (ADS)

    Sripathi Panditaradhyula, Anuhya

    The need for resin with a long clinical life can be satiated through the novel formulation of varying concentrations of oxirane and acrylate monomers with an increase in filler loading in the sample, which will allow the creation of a resin that is less susceptible to chemical degradation along with improved mechanical properties. Various concentrations of oxirane and acrylate monomers with a three-component photoinitiation system, which is capable of both free radical (acrylate) and cationic (oxirane) initiation, are used. The resin composites were placed in the Speedmixer for 30 seconds and gravitation convection oven for one minute, repeated 5-7 times. The resin composites were used to create a 9.525 mm diameter * 1.5875 mm thick resin mold. The mold was then photocured for twenty seconds on both sides using VALO blue LED light. The Rockwell hardness and shore D durometer hardness served as relative measures of bonding between the monomers. The ideal formulation of oxirane and acrylate concentrations were used to perform the Instron 3 point bend test, as well as contact angle determination. The goal is to identify a resin with a clinical life twice that of the resins being used in practice. Potential findings include ideal oxirane and acrylate concentrations with the highest shore D durometer hardness, Rockwell hardness, contact angle values, and Instron 3 point bend test values. Ideal color, transparency and properties of the resin are taken into account. Optimization of oxirane and acrylate monomers, impact while using various filler components (salination, number of fillers), filler particle size variations and variations in using different filler concentrations are observed. Results of using micro and nano-sized monomers are also studied. Addition of fluorinated acrylate monomer to the micro and nano composite was the next goal. A comparison of all the above stated compositions to the control group 70/30 BisTEG was done. A study on the degradation behavior

  1. Evaluation of poly(acrylic acid-co-ethylhexyl acrylate) films for mucoadhesive transbuccal drug delivery: factors affecting the force of mucoadhesion.

    PubMed

    Shojaei, A H; Paulson, J; Honary, S

    2000-07-03

    Based on the premise that similar surface properties between the adhesive and the substrate would yield a strong adhesive bond, copolymers of acrylic acid (AA) and 2-ethylhexyl acrylate (EHA), P(AA-co-EHA), were designed and synthesized for buccal mucoadhesion. A series of linear copolymers with varying feed ratios of the two monomers (AA and EHA) were synthesized through free radical copolymerization at 69+/-0.5 degrees C using azobis(isobutyronitrile) (AIBN) as initiator. The reactions were carried out in THF under nitrogen for 24 h. The glass transition temperatures, T(g), of the copolymers were determined using DSC. The adhesion studies were conducted to determine the effects of copolymer composition, contact time between the substrate and the adhesive, and crosshead speed on mucoadhesive performance of the copolymer films using a computer interfaced Instron material testing system. The glass transition temperature of the copolymers decreased with increasing EHA content. Wet glass surface as substrate was shown not to be a good substrate model for adhesion determination studies. The copolymer composed of 46:54 mol.% AA:EHA (an almost 1:1 ratio in the repeat units) yielded the highest mucoadhesive force in contact with porcine buccal mucosa which was significantly greater (P<0.05) than that of poly(acrylic acid) (PAA) (used as positive control). The mucoadhesive force for all copolymers studied was significantly (P<0.05) greater than that of the negative control (backing material without copolymer film) except for the EHA homopolymer. Crosshead speed increased mucoadhesive force linearly and had a more pronounced effect on the mucoadhesive performance than time of contact between the adhesive and the substrate.

  2. Nail Damage (Severe Onychodystrophy) Induced by Acrylate Glue: Scanning Electron Microscopy and Energy Dispersive X-Ray Investigations

    PubMed Central

    Pinteala, Tudor; Chiriac, Anca Eduard; Rosca, Irina; Larese Filon, Francesca; Pinteala, Mariana; Chiriac, Anca; Podoleanu, Cristian; Stolnicu, Simona; Coros, Marius Florin; Coroaba, Adina

    2017-01-01

    Background Scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) techniques have been used in various fields of medical research, including different pathologies of the nails; however, no studies have focused on obtaining high-resolution microscopic images and elemental analysis of disorders caused by synthetic nails and acrylic adhesives. Methods Damaged/injured fingernails caused by the use of acrylate glue and synthetic nails were investigated using SEM and EDX methods. Results SEM and EDX proved that synthetic nails, acrylic glue, and nails damaged by contact with acrylate glue have a different morphology and different composition compared to healthy human nails. Conclusions SEM and EDX analysis can give useful information about the aspects of topography (surface sample), morphology (shape and size), hardness or reflectivity, and the elemental composition of nails. PMID:28232921

  3. Evidence of octacalcium phosphate and Type-B carbonated apatites deposited on the surface of explanted acrylic hydrogel intraocular lens.

    PubMed

    Lin, Shan-Yang; Chen, Ko-Hua; Li, May-Jane; Cheng, Wen-Ting; Wang, Shun-Li

    2004-08-15

    Fourier-transform infrared (FTIR) microspectroscopy combining with attenuated total reflection (ATR) microsampling technique and micro-Raman spectrophotometer were used to detect the deposited materials on the surface of acrylic hydrogel intraocular lens (IOL) with or without ocular implantation. Surface morphology and the interface of this IOL were further examined by a confocal laser scanning microscope. The brand-new IOL exhibited a very smooth, transparent and featureless surface, but the explanted IOL had an irregular cerebriform-like opaque appearance. Both FTIR/ATR and Raman microspectroscopic analyses showed the deposits on the surface of acrylic hydrogel IOL after ocular implantation to consist of octacalcium phosphate (OCP) and Type B carbonated apatites, leading to the opalescence of acrylic hydrogel IOL. Both vibrational microspectroscopic examinations also confirmed the mineralization still in progress on the surface of acrylic hydrogel IOL after ocular implantation for 2 years.

  4. Taste sensing with polyacrylic acid grafted cellulose membrane.

    PubMed

    Majumdar, Sarmishtha; Dey, Joykrishna; Adhikari, Basudam

    2006-03-15

    There are reports of fabrication of taste sensor by adsorbing lipids into Millipore filter paper, which improved the taste sensing efficiency of membrane remarkably. We have made an attempt to prepare taste sensor material by grafting polyacrylic acid (PAA) to cellulose. The research work covers polymer membrane preparation, morphology study, and structural characterization of the membrane and study of the taste sensing characteristics of this membrane for five different taste substances. FTIR spectroscopic analysis and SEM were done to get an idea about the structure and morphology of the PAA grafted cellulose membrane. Surface charge density of the membrane was estimated. The sensor characteristics like temporal stability, response stability, response to different taste substances, and reproducibility of sensing performance were studied using PAA grafted cellulose membrane. Sensor device prepared with this membrane has shown distinct response patterns for different taste substances in terms of membrane potential. Threshold concentrations of PAA grafted cellulose membrane for HCl, NaCl, quinine-hydrochloride (Q-HCl), sucrose and monosodium glutamate are 0.001 mM, 0.01 mM, 0.08 mM, 0.08 mM and 0.01 mM, respectively. The threshold concentrations except that in Q-HCl are below human threshold concentrations. Membranes also showed characteristic response patterns for organic acids like acetic acid, citric acid, formic acid, etc., mineral acids like HCl, H(2)SO(4) and HNO(3), etc., salts, bitter substances, sweet substances and umami substances. Sensor device prepared with this membrane has excellent shelf life.

  5. Double-bond-containing polyallene-based triblock copolymers via phenoxyallene and (meth)acrylate.

    PubMed

    Ding, Aishun; Lu, Guolin; Guo, Hao; Huang, Xiaoyu

    2017-03-02

    A series of ABA triblock copolymers, consisting of double-bond-containing poly(phenoxyallene) (PPOA), poly(methyl methacrylate) (PMMA), or poly(butyl acrylate) (PBA) segments, were synthesized by sequential free radical polymerization and atom transfer radical polymerization (ATRP). A new bifunctional initiator bearing azo and halogen-containing ATRP initiating groups was first prepared followed by initiating conventional free radical homopolymerization of phenoxyallene with cumulated double bond to give a PPOA-based macroinitiator with ATRP initiating groups at both ends. Next, PMMA-b-PPOA-b-PMMA and PBA-b-PPOA-b-PBA triblock copolymers were synthesized by ATRP of methyl methacrylate and n-butyl acrylate initiated by the PPOA-based macroinitiator through the site transformation strategy. These double-bond-containing triblock copolymers are stable under UV irradiation and free radical circumstances.

  6. Peel/seal properties of poly(ethylene methyl acrylate)/polybutene-1 blend films

    NASA Astrophysics Data System (ADS)

    Mohammdi, Seyedeh Raziyeh; Ajji, Abdellah; Tabatabaei, Seyed H.

    2015-05-01

    Nowadays, the possibility to easy open a food package is of great interest both from the consumer and food producers' perspective. In this study, the peel/seal properties of poly (ethylene methyl acrylate) (EMA)/polybutene-1 (PB-1) blend films were investigated. Three blends of EMA/PB-1 with different methyl acrylate (MA) content were prepared using cast extrusion process. Differential Scanning Calorimetry (DSC) was used to investigate the thermal behavior as well as the crystalinity of the blends. The effect of polymer matrix on the crystalline structure of PB-1 was studied using Wide Angle X-ray Diffraction (WAXD) and DSC. T-peel tests were carried out on the heat sealed films at various seal temperatures. The effect of MA content and heat seal temperature on peel/seal properties (i.e. peel initiation temperature, temperature window of sealability and peel strength) of the films were studied.

  7. Double-bond-containing polyallene-based triblock copolymers via phenoxyallene and (meth)acrylate

    NASA Astrophysics Data System (ADS)

    Ding, Aishun; Lu, Guolin; Guo, Hao; Huang, Xiaoyu

    2017-03-01

    A series of ABA triblock copolymers, consisting of double-bond-containing poly(phenoxyallene) (PPOA), poly(methyl methacrylate) (PMMA), or poly(butyl acrylate) (PBA) segments, were synthesized by sequential free radical polymerization and atom transfer radical polymerization (ATRP). A new bifunctional initiator bearing azo and halogen-containing ATRP initiating groups was first prepared followed by initiating conventional free radical homopolymerization of phenoxyallene with cumulated double bond to give a PPOA-based macroinitiator with ATRP initiating groups at both ends. Next, PMMA-b-PPOA-b-PMMA and PBA-b-PPOA-b-PBA triblock copolymers were synthesized by ATRP of methyl methacrylate and n-butyl acrylate initiated by the PPOA-based macroinitiator through the site transformation strategy. These double-bond-containing triblock copolymers are stable under UV irradiation and free radical circumstances.

  8. Cold-plasma assisted grafting of cellulose fibres by acrylic monomers

    NASA Astrophysics Data System (ADS)

    Gaiolas, Carla; Amaral, Maria Emilia; Costa, Ana Paula; Santos Silva, Manuel José; Belgacem, Mohamed Naceur

    2012-07-01

    Additive-free hand sheet paper samples were activated by cold-plasma in the presence of acrylic acid (AAc), acrylamide (AAm), methyl acrylate (MAc) and methyl methacrylate (MMa). The characterisation of the modified substrates showed that there grafting has occurred efficiently, as established by weight gain and FTIR spectroscopy. The contact angle measurement were carried out, as a function of pH and showed that the deposition of a drop of water at the surface of the tested samples formed 55° for unmodified substrate to 87°, for MMa-treated papers, respectively, indicating that the surface has became totally hydrophobic. ATR-FTIR spectroscopy was used to check the grafting efficiency.

  9. Synthesis evaluation and adsorption studies of anionic copolymeric surfactants based on fatty acrylate ester

    NASA Astrophysics Data System (ADS)

    El-Dougdoug, W. I. A.; El-Mossalamy, E. H.

    2006-12-01

    A series of anionic copolymeric surfactants based on n-dodecylacrylate ester (M 1) as hydrophobe, and oxypropylated acrylate ester (MA 4,6) as hydrophiles, were prepared by copolymerization of n-dodecylacrylate (M 1) and oxypropylated acrylate ester (MA 4,6) with molar ratio's (0.3:0.7, 0.4:0.6 and 0.5:0.5, respectively) in presence of benzoyl peroxide as initiator followed by sulfation and neutralization to afforded [(PAS 4), and (PAS 6)] a-c, as anionic copolymeric surfactant in suitable yield. These derivatives were purified and characterized by IR and 1H NMR spectral studies. Surface activity, and biodegradability were evaluated. Adsorption of some copolymeric surfactant on salary sand was investigated to assess possibility of treating waste water streams for removal of Pb 2+ and Hg 2+ toxic minerals. The effect of several factors governing the adsorption such as initial concentration, temperature, pH, have been studied.

  10. Double-bond-containing polyallene-based triblock copolymers via phenoxyallene and (meth)acrylate

    PubMed Central

    Ding, Aishun; Lu, Guolin; Guo, Hao; Huang, Xiaoyu

    2017-01-01

    A series of ABA triblock copolymers, consisting of double-bond-containing poly(phenoxyallene) (PPOA), poly(methyl methacrylate) (PMMA), or poly(butyl acrylate) (PBA) segments, were synthesized by sequential free radical polymerization and atom transfer radical polymerization (ATRP). A new bifunctional initiator bearing azo and halogen-containing ATRP initiating groups was first prepared followed by initiating conventional free radical homopolymerization of phenoxyallene with cumulated double bond to give a PPOA-based macroinitiator with ATRP initiating groups at both ends. Next, PMMA-b-PPOA-b-PMMA and PBA-b-PPOA-b-PBA triblock copolymers were synthesized by ATRP of methyl methacrylate and n-butyl acrylate initiated by the PPOA-based macroinitiator through the site transformation strategy. These double-bond-containing triblock copolymers are stable under UV irradiation and free radical circumstances. PMID:28252049

  11. Rate constants of the reactions of ozone with nitriles, acrylates and terpenes in gas phase

    NASA Astrophysics Data System (ADS)

    Munshi, Hushider B.; Rao, K. V. S. Rama; Iyer, R. Mahadeva

    Rate constants for the reactions of acrylonitrile, methacrylonitrile, methyl and ethyl acrylate with O 3 have been determined with the help of a flow system coupled to an u.v. spectrophotometer. The rate constants obtained have enabled an estimation of the tropospheric lifetimes with respect to O 3 and have also offered a clue to the nature of the initial ozone attack on the unsaturates. Non-stoichiometry observed in the case of acrylonitrile and ethyl acrylate has been rationalized by secondary free radical reactions. Absorptivities of the four unsaturates in vapour as well as in the solution phase have been reported. A brief attempt to study ozone-terpene reactions is also described.

  12. Acrylate intercalation and in situ polymerization in iron-, cobalt-, or manganese-substituted nickel hydroxides.

    PubMed

    Vaysse, C; Guerlou-Demourgues, L; Duguet, E; Delmas, C

    2003-07-28

    A chimie douce route based on successive redox and exchange reactions has allowed us to prepare new hybrid organic-inorganic materials, composed of polyacrylate macromolecules intercalated into layered double hydroxides (LDHs), deriving from Ni(OH)(2). Monomer intercalation and in situ polymerization mechanisms have appeared to be strongly dependent upon the nature of the substituting cation in the slabs. In the case of iron-based LDHs, a phase containing acrylate monomeric intercalates has been isolated and identified by X-ray diffraction and infrared spectroscopy. Second, interslab free-radical polymerization of acrylate anions has been successfully initiated using potassium persulfate. In cobalt- or manganese-based LDHs, one-step polymerization has been observed, leading directly to a material containing polyacrylate intercalate.

  13. Peel/seal properties of poly(ethylene methyl acrylate)/polybutene-1 blend films

    SciTech Connect

    Mohammdi, Seyedeh Raziyeh; Ajji, Abdellah; Tabatabaei, Seyed H.

    2015-05-22

    Nowadays, the possibility to easy open a food package is of great interest both from the consumer and food producers’ perspective. In this study, the peel/seal properties of poly (ethylene methyl acrylate) (EMA)/polybutene-1 (PB-1) blend films were investigated. Three blends of EMA/PB-1 with different methyl acrylate (MA) content were prepared using cast extrusion process. Differential Scanning Calorimetry (DSC) was used to investigate the thermal behavior as well as the crystalinity of the blends. The effect of polymer matrix on the crystalline structure of PB-1 was studied using Wide Angle X-ray Diffraction (WAXD) and DSC. T-peel tests were carried out on the heat sealed films at various seal temperatures. The effect of MA content and heat seal temperature on peel/seal properties (i.e. peel initiation temperature, temperature window of sealability and peel strength) of the films were studied.

  14. Real-time monitoring of graphene oxide reduction in acrylic printable composite inks

    NASA Astrophysics Data System (ADS)

    Porro, S.; Giardi, R.; Chiolerio, A.

    2014-06-01

    This work reports the electrical characterization of a water-based graphene oxide/acrylic composite material, which was directly inkjet printed to fabricate dissipative patterns. The graphene oxide filler, which is strongly hydrophilic due to its heavily oxygenated surface and can be readily dispersed in water, was reduced by UV irradiation during photo-curing of the polymeric matrix. The concurrent polymerization of the acrylic matrix and reduction of graphene oxide filler was demonstrated by real-time resistance measurements during UV light irradiation. The presence of graphene filler allowed decreasing the resistance of the pure polymeric matrix by nearly five orders of magnitude. This was explained by the fact that clusters of reduced graphene oxide inside the polymer matrix act as preferential pathways for the mobility of charge carriers, thus leading to an overall decrease of the material's resistance.

  15. Preparation of metal adsorbent from poly(methyl acrylate)-grafted-cassava starch via gamma irradiation

    NASA Astrophysics Data System (ADS)

    Suwanmala, Phiriyatorn; Hemvichian, Kasinee; Hoshina, Hiroyuki; Srinuttrakul, Wannee; Seko, Noriaki

    2012-08-01

    Metal adsorbent containing hydroxamic acid groups was successfully synthesized by radiation-induced graft copolymerization of methyl acrylate (MA) onto cassava starch. The optimum conditions for grafting were studied in terms of % degree of grafting (Dg). Conversion of the ester groups present in poly(methyl acrylate)-grafted-cassava starch copolymer into hydroxamic acid was carried out by treatment with hydroxylamine (HA) in the presence of alkaline solution. The maximum percentage conversion of the ester groups of the grafted copolymer, % Dg=191 (7.63 mmol/g of MA), into the hydroxamic groups was 70% (5.35 mmol/g of MA) at the optimum condition. The adsorbent of 191%Dg had total adsorption capacities of 2.6, 1.46, 1.36, 1.15 and 1.6 mmol/g-adsorbent for Cd2+, Al3+, UO22+, V5+ and Pb2+, respectively, in the batch mode adsorption.

  16. Influence of Surface Properties on the Adhesion of Staphylococcus epidermidis to Acrylic and Silicone

    PubMed Central

    Sousa, Cláudia; Teixeira, Pilar; Oliveira, Rosário

    2009-01-01

    The aim of the present study was to compare the ability of eight Staphylococcus epidermidis strains to adhere to acrylic and silicone, two polymers normally used in medical devices manufacture. Furthermore, it was tried to correlate that with the surface properties of substrata and cells. Therefore, hydrophobicity and surface tension components were calculated through contact angle measurements. Surface roughness of substrata was also assessed by atomic force microscopy (AFM). No relationship was found between microbial surface hydrophobicity and adhesion capability. Nevertheless, Staphylococcus epidermidis IE214 showed very unique adhesion behaviour, with cells highly aggregated between them, which is a consequence of their specific surface features. All strains, determined as being hydrophilic, adhered at a higher extent to silicone than to acrylic, most likely due to its more hydrophobic character and higher roughness. This demonstrates the importance of biomaterial surface characteristics for bacterial adhesion. PMID:20126579

  17. Effect of microwave disinfection on mechanical properties of denture base acrylic resin.

    PubMed

    Hamouda, Ibrahim M; Ahmed, Sabry A

    2010-10-01

    The microwave oven was used for sterilizing dentures contaminated with Candida albicans and other communicable diseases instead of disinfectant solutions. This study was carried out to evaluate the flexural properties, toughness, and impact strength of heat-cured acrylic resin sterilized by microwave oven either immersed in water or non-immersed for 5 and 15 min at full power. The results indicated that the microwave oven sterilization technique resulted in reduction of the load necessary to fracture the specimens, deformation at fracture, transverse strength, modulus of elasticity except disinfection at 5 min dry condition, toughness, and impact strength. This study concluded that the microwave oven is not acceptable for sterilization of dentures because of its weakening effects on the dentures that prone for fracture during clinical use. This method of sterilization increased the brittleness of acrylic resin specimens.

  18. Pluronic-poly (acrylic acid)-cysteine/Pluronic L121 mixed micelles improve the oral bioavailability of paclitaxel.

    PubMed

    Zhao, Yanli; Li, Yanli; Ge, Jianjun; Li, Na; Li, Ling-Bing

    2014-11-01

    The aim of the study is to synthesize a thiolated Pluronic copolymer, Pluronic-poly (acrylic acid)-cysteine copolymer, to construct a mixed micelle system with the Pluronic-poly (acrylic acid)-cysteine copolymer and Pluronic L121 (PL121) and to evaluate the potential of these mixed micelles as an oral drug delivery system for paclitaxel. Compared with Pluronic-poly (acrylic acid)-cysteine micelles, drug-loading capacity of Pluronic-poly (acrylic acid)-cysteine/PL121 mixed micelles was increased from 0.4 to 2.87%. In vitro release test indicated that Pluronic-poly (acrylic acid)-cysteine/PL121 mixed micelles exhibited a pH sensitivity. The permeability of drug-loaded micelles in the intestinal tract was studied with an in situ perfusion method in rats. The presence of verapamil and Pluronic both improved the intestinal permeability of paclitaxel, which further certified the inhibition effect of thiolated Pluronic on P-gp. In pharmacokinetic study, the area under the plasma concentration-time curve (AUC0→∞) of paclitaxel-loaded mixed micelles was four times greater than that of the paclitaxel solution (p < 0.05). In general, Pluronic-poly (acrylic acid)-cysteine/PL121 micelles were proven to be a potential oral drug delivery system for paclitaxel.

  19. Synthesis and electromechanical characterization of a new acrylic dielectric elastomer with high actuation strain and dielectric strength

    NASA Astrophysics Data System (ADS)

    Hu, Wei; Niu, Xiaofan; Yang, Xinguo; Zhang, Naifang; Pei, Qibing

    2013-04-01

    Dielectric Elastomers (DEs) can be actuated under high electric field to produce large strains. Most high-performing DE materials such as the 3M™ VHB™ membranes are commercial products designed for industrial pressure-sensitive adhesives. The limited knowledge of the exact chemical structures of these commercial materials has made it difficult to understand the relationship between molecular structures and electromechanical properties. In this work, new acrylic elastomers based on n-butyl acrylate and acrylic acid were synthesized from monomer solutions by UV-initiated bulk polymerization. The new acrylic copolymers have a potential to obtain high dielectric constant, actuation strain, dielectric strength, and a high energy density. Silicone and ester oligomer diacrylates were also added onto the copolymer structures to suppress crystallization and to crosslink the polymer chains. Four acrylic formulations were developed with different amounts of acrylic acid. This gives a tunable stiffness, while the dielectric constant is varied from 4.3 to 7.1. The figure-of-merit performance of the best formulation is 186 % area strain, 222 MV/m of dielectric strength, and 2.7 MJ/m3 of energy density. To overcome electromechanical instability, different prestrain ratios were investigated, and under the optimized prestrain, the material has a lifetime of thousands of cycles at 120 % area strain.

  20. A Study on Effect of Surface Treatments on the Shear Bond Strength between Composite Resin and Acrylic Resin Denture Teeth.

    PubMed

    Chatterjee, Nirmalya; Gupta, Tapas K; Banerjee, Ardhendu

    2011-03-01

    Visible light-cured composite resins have become popular in prosthetic dentistry for the replacement of fractured/debonded denture teeth, making composite denture teeth on partial denture metal frameworks, esthetic modification of denture teeth to harmonize with the characteristics of adjacent natural teeth, remodelling of worn occlusal surfaces of posterior denture teeth etc. However, the researches published on the bond strength between VLC composite resins and acrylic resin denture teeth is very limited. The purpose of this study is to investigate the effect of five different methods of surface treatments on acrylic resin teeth on the shear bond strength between light activated composite resin and acrylic resin denture teeth. Ninety cylindrical sticks of acrylic resin with denture teeth mounted atop were prepared. Various treatments were done upon the acrylic resin teeth surfaces. The samples were divided into six groups, containing 15 samples each. Over all the treated and untreated surfaces of all groups, light-cured composite resin was applied. The shear strengths were measured in a Universal Testing Machine using a knife-edge shear test. Data were analyzed using one way analysis of variance (ANOVA) and mean values were compared by the F test. Application of bonding agent with prior treatment of methyl methacrylate on the acrylic resin denture teeth resulted in maximum bond strength with composite resin.

  1. Effect of water-aging on the antimicrobial activities of an ORMOSIL-containing orthodontic acrylic resin

    PubMed Central

    Gong, Shi-qiang; Epasinghe, D. Jeevanie; Zhou, Bin; Niu, Li-na; Kimmerling, Kirk A.; Rueggeberg, Frederick A.; Yiu, Cynthia K.Y.; Mao, Jing; Pashley, David H.; Tay, Franklin R.

    2013-01-01

    Quaternary ammonium methacryloxy silicate (QAMS), an organically modified silicate (ORMOSIL) functionalized with polymerizable methacrylate groups and an antimicrobial agent with a long lipophilic alkyl chain quaternary ammonium group, was synthesized through a silane-based sol–gel route. By dissolving QAMS in methyl methacrylate monomer, this ORMOSIL molecule was incorporated into an auto-polymerizing, powder/liquid orthodontic acrylic resin system, yielding QAMS-containing poly (methyl methacrylate). The QAMS-containing acrylic resin showed a predominant contact-killing effect on Streptococcus mutans (ATCC 35668) and Actinomyces naeslundii (ATCC 12104) biofilms, while inhibiting adhesion of Candida albicans (ATCC 90028) on the acrylic surface. The antimicrobial activities of QAMS-containing acrylic resin were maintained after a 3 month water-aging period. Bromophenol blue assay showed minimal leaching of quaternary ammonium species when an appropriate amount of QAMS (<4 wt.%) was incorporated into the acrylic resin. The results suggest that QAMS is predominantly co-polymerized with the poly(methyl methacrylate) network, and only a minuscule amount of free QAMS molecules is present within the polymer network after water-aging. Acrylic resin with persistent antimicrobial activities represents a promising method for preventing bacteria- and fungus-induced stomatitis, an infectious disease commonly associated with the wearing of removable orthodontic appliances. PMID:23485857

  2. Relationship between cell surface composition of Candida albicans and adherence to acrylic after growth on different carbon sources.

    PubMed Central

    McCourtie, J; Douglas, L J

    1981-01-01

    The adherence of Candida albicans to acrylic was measured in vitro after growth of the yeast to stationary phase in defined medium containing glucose, sucrose, galactose, fructose, or maltose as the carbon source. In each case, yeast adherence was proportional to the concentration of sugar in the growth medium, but equimolar concentrations of different sugars promoted adherence to different extents. In vitro adherence was further increased by the addition of divalent cations to assay mixtures but was inhibited when saliva-treated acrylic strips were used or when yeasts were suspended in mixed saliva during the assay. The rate of spheroplast formation of yeasts grown in media containing a 500 mM concentration of the different sugars correlated well with the relative adherence of the cells to acrylic. Galactose-grown yeasts were most resistant to spheroplast formation with Zymolyase-5000 and most adherent to acrylic, whereas fructose-grown organisms were least resistant to spheroplast formation and least adherent to acrylic. These results indicate that when grown to stationary phase in media containing high concentrations of certain sugars, C. albicans undergoes a change in cell surface composition which facilitates its adherence to acrylic surfaces. Electron microscopy of yeasts harvested from such media revealed the presence of an additional surface layer which may be responsible for this enhanced adherence. Images PMID:7019091

  3. The intensity of immunogold labeling of deplasticized acrylic sections compared to deplasticized epoxy sections-Theoretical deductions and experimental data.

    PubMed

    Brorson, Sverre-Henning; Reinholt, Finn P

    2008-01-01

    The purpose of this study was to compare the level of immunogold labeling of deplasticized acrylic sections and deplasticized epoxy sections. Pure protein gels of IgG, albumin and thyroglobulin were produced by glutaraldehyde fixation and embedded in non-crosslinked acrylic resin (Technovit 9100) and epoxy resin (Epon 812), respectively. Ultrathin sections of acrylic and epoxy resin were separately deplasticized in 2-methoxyethyl acetate (MEA) and sodium ethoxide. Quantitative immunogold labeling was performed with anti-IgG, anti-albumin and anti-thyroglobulin antibodies on sections of the corresponding protein gels. For all antibodies tested, the intensity of labeling for deplasticized acrylic sections was significantly higher (two to four times) than for the corresponding deplasticized epoxy sections. The results fit with a theoretically deduced relation: the quotient of the labeling of two deplasticized sections of different resins is equivalent to the square root of the quotient of the labeling of the similar sections not exposed to any kind of pre-treatment. The practical significance of the results is that immunolabeling of deplasticized non-crosslinked acrylic resin results in more intense immunogold labeling than deplasticized epoxy sections. Deplasticizing is most useful when the requirements for ultrastructural preservation according to conventional criteria are moderate. Our theoretically deduced results also indicate that deplasticized Technovit (or other non-crosslinked acrylic resins) sections will be significantly better suited for immunolabeling at the light microscopic level than deplasticized epoxy sections.

  4. Nonlinear Optical Acrylic Polymers and Use Thereof in Optical and Electro-Optic Devices

    DTIC Science & Technology

    1992-01-07

    COVERED 4. TITLE AND SUBTITLE Nonlinear Optical Acrylic Polymers and Use Thereof in Optical and Electro - Optic Devices 5a. CONTRACT NUMBER 5b. GRANT...generators, computational devices and the like. 15. SUBJECT TERMS optical devices, electro - optical devices, optical signal processing...THEREOF IN OPTICAL AND ELECTRO - OPTIC DEVICES [75] Inventors: Le*lie H. Sperling, Bethlehem; Clarence J. Murphy, Stroudsburg; Warren A. Rosen

  5. Modification of polyethylene by radiation-induced graft polymerization of acrylic acid

    NASA Astrophysics Data System (ADS)

    Sidorova, L. P.; Aliev, A. D.; Zlobin, V. B.; Aliev, R. E.; Chalykh, A. E.; Kabanov, V. Ya.

    The kinetics investigation of the radiation-induced graft polymerization of acrylic acid onto low density polyethylene by direct method in aqueous solution in the presence of Mohr's salt, was performed. The technique of the contrasting of polyacrylic acid (PAA) graft layer was worked out by Ag +-ions. The structural and morphological peculiarities of grafted copolymers of PE with PAA were determined by the method of electron probe, and X-ray microanalysis by means of the electron microscopy.

  6. An innovative technique for customizing the stock acrylic resin ocular prosthesis.

    PubMed

    Mowade, Tushar K; Dange, S P

    2011-01-01

    The loss of an eye is a traumatic and common event. The psychological effects of losing an eye are frequently more difficult to deal with than its functional loss. This article describes the management of a child patient with anopthalmic socket, by an innovative technique of customizing the stock acrylic resin ocular prosthesis to get improved esthetics, accurate location of iris-pupil complex and exact fit in the defect.

  7. Characterization and bacterial anti-adherent effect on modified PMMA denture acrylic resin containing platinum nanoparticles

    PubMed Central

    2014-01-01

    PURPOSE This study characterized the synthesis of a modified PMMA (Polymethyl methacrylate) denture acrylic loading platinum nanoparticles (PtN) and assessed its bacterial inhibitory efficacy to produce novel antimicrobial denture base material. MATERIALS AND METHODS Polymerized PMMA denture acrylic disc (20 mm × 2 mm) specimens containing 0 (control), 10, 50, 100 and 200 mg/L of PtN were fabricated respectively. The obtained platinum-PMMA nanocomposite (PtNC) was characterized by TEM (transmission electron microscopy), SEM/EDX (scanning electron microscope/energy dispersive X-ray spectroscopy), thermogravimetric and atomic absorption spectrophotometer analysis. In antimicrobial assay, specimens were placed on the cell culture plate, and 100 µL of microbial suspensions of S. mutans (Streptococcus mutans) and S. sobrinus (Streptococcus sobrinus) were inoculated then incubated at 37℃ for 24 hours. The bacterial attachment was tested by FACS (fluorescence-activated cell sorting) analysis after staining with fluorescent probe. RESULTS PtN were successfully loaded and uniformly immobilized into PMMA denture acrylic with a proper thermal stability and similar surface morphology as compared to control. PtNC expressed significant bacterial anti-adherent effect rather than bactericidal effect above 50 mg/L PtN loaded when compared to pristine PMMA (P=.01) with no or extremely small amounts of Pt ion eluted. CONCLUSION This is the first report on the synthesis and its antibacterial activity of Pt-PMMA nanocomposite. PMMA denture acrylic loading PtN could be a possible intrinsic antimicrobial denture material with proper mechanical characteristics, meeting those specified for denture bases. For clinical application, future studies including biocompatibility, color stability and warranting the long-term effect were still required. PMID:25006385

  8. Investigation of the Pour Point Depression Ability of Polyalkyl Acrylate Additives After Sonication

    NASA Astrophysics Data System (ADS)

    Volkova, G. I.; Anufriev, R. V.; Yudina, N. V.; Tchaikovskaya, O. N.

    2016-12-01

    Effect of ultrasonic treatment on the molecular parameters of polymeric additives based on polyalkyl acrylate is investigated. The viscosity, temperature, and energy characteristics of high-wax crude oil and solutions of petroleum wax in decane and aviation fuel TS-1 in the presence of initial and ultrasonified additives are determined. Results obtained indicate that the pour point depression ability of the additives is not reduced after treatment in an ultrasonic field.

  9. Inhibition of the polymerization of methyl methacrylate and methyl acrylate by mixtures of chloranil with phenothiazine

    SciTech Connect

    Ivanov, A.A; Lysenko, G.M.; Zholina, I.N.

    1985-09-01

    This paper investigates the kinetic peculiarities of inhibited polymerization of methyl methacrylate and methyl acrylate in the presence of mixtures of chloranil with phenothiazine. It is shown that depending on the structure of the monomer and the concentrations of the electron donor and electron acceptor, the radicals of propagation may form complexes with chloranil or with phenothiazine at the first step of the inhibition reaction or may interact with the complex (phenothiazine to chloranil).

  10. Structure and properties of poly(benzyl acrylate) synthesized under microwave energy

    NASA Astrophysics Data System (ADS)

    Oberti, Tamara G.; Schiavoni, M. Mercedes; Cortizo, M. Susana

    2008-05-01

    Benzyl acrylate was polymerized under microwave irradiation using radical initiation (benzoyl peroxide, BP). The effect of the concentration of BP and power irradiation on the conversion, average molecular weights and the polydispersity index ( Mw/ Mn) were investigated. The 1H NMR and 13C NMR spectra analysis showed tendency to syndiotacticity and branched polymers were obtained at high conversion of reactions. A significant enhancement of the rates of polymerization and similar thermodynamic behavior, as compared with those obtained under thermal conditions was found.

  11. Synthesis of Hydroxy-Terminated Dinitropropyl Acrylate Polymers and Improved Characterization of Hydroxy-Terminated Prepolymers

    DTIC Science & Technology

    1983-03-01

    azelate polyesterdiol from Wittco PA Phthalic anhydride PCP Polycaprolactone diol from Union Carbide PDNPA Polydinitropropyl acrylate (our experimental... anhydride (AA) in the presence of N-methylimidazole (NMIM) (15)reported by Conners , and (b) phthalic anhydride (PA) in the presence of pyridine (PY...three meq sample of dried polymer was weighed into a 100 ml round bottom flask and 50 ml of phthalic anhydride stock solution (0.6 N) in anhydrous

  12. One-step formation of multiple Pickering emulsions stabilized by self-assembled poly(dodecyl acrylate-co-acrylic acid) nanoparticles.

    PubMed

    Zhu, Ye; Sun, Jianhua; Yi, Chenglin; Wei, Wei; Liu, Xiaoya

    2016-09-13

    In this study, a one-step generation of stable multiple Pickering emulsions using pH-responsive polymeric nanoparticles as the only emulsifier was reported. The polymeric nanoparticles were self-assembled from an amphiphilic random copolymer poly(dodecyl acrylate-co-acrylic acid) (PDAA), and the effect of the copolymer content on the size and morphology of PDAA nanoparticles was determined by dynamic light scattering (DLS) and transmission electron microscopy (TEM). The emulsification study of PDAA nanoparticles revealed that multiple Pickering emulsions could be generated through a one-step phase inversion process by using PDAA nanoparticles as the stabilizer. Moreover, the emulsification performance of PDAA nanoparticles at different pH values demonstrated that multiple emulsions with long-time stability could only be stabilized by PDAA nanoparticles at pH 5.5, indicating that the surface wettability of PDAA nanoparticles plays a crucial role in determining the type and stability of the prepared Pickering emulsions. Additionally, the polarity of oil does not affect the emulsification performance of PDAA nanoparticles, and a wide range of oils could be used as the oil phase to prepare multiple emulsions. These results demonstrated that multiple Pickering emulsions could be generated via the one-step emulsification process using self-assembled polymeric nanoparticles as the stabilizer, and the prepared multiple emulsions have promising potential to be applied in the cosmetic, medical, and food industries.

  13. Acrylic AB and ABA block copolymers based on poly(2-ethylhexyl acrylate) (PEHA) and poly(methyl methacrylate) (PMMA) via ATRP.

    PubMed

    Haloi, Dhruba J; Ata, Souvik; Singha, Nikhil K; Jehnichen, Dieter; Voit, Brigitte

    2012-08-01

    Acrylic block copolymers have several advantages over conventional styrenic block copolymers, because of the presence of a saturated backbone and polar pendant groups. This investigation reports the preparation and characterization of di- and triblock copolymers (AB and ABA types) of 2-ethylhexyl acrylate (EHA) and methyl methacrylate (MMA) via atom transfer radical polymerization (ATRP). A series of block copolymers, PEHA-block-PMMA(AB diblock) and PMMA-block-PEHA-block-PMMA(ABA triblock) were prepared via ATRP at 90 °C using CuBr as catalyst in combination with N,N,N',N″,N″-pentamethyl diethylenetriamine (PMDETA) as ligand and acetone as additive. The chemical structure of the macroinitiators and molar composition of block copolymers were characterized by (1)H NMR analysis, and molecular weights of the polymers were analyzed by GPC analysis. DSC analysis showed two glass transition temperatures (T(g)), indicating formation of two domains, which was corroborated by AFM analysis. Small-angle X-ray scattering (SAXS) analysis of AB and ABA block copolymers showed scattering behavior inside the measuring limits indicating nanophase separation. However, SAXS pattern of AB diblock copolymers indicated general phase separation only, whereas for ABA triblock copolymer an ordered or mixed morphology could be deduced, which is assumed to be the reason for the better mechanical properties achieved with ABA block copolymers than with the AB analogues.

  14. Characterizing acrylic pressure-sensitive adhesive tapes favoring diverse biomedical applications

    NASA Astrophysics Data System (ADS)

    Alhijji, Saleh Mohammed S.

    Strong, self-adhesive acrylic polymer-based tapes have been identified as FDA-approved medical device construction components that might also serve in diverse biological locations as artificial muscles, ligaments, or compressive support discs. After assuring that the tapes themselves were not cytotoxic, they were evaluated as possible low-tension muscle substitutes for eyelids, jaws, and other modest body re-closing needs, and well as for higher-tension applications as artificial ligaments. Self-adhesion of the tapes to representative biomaterials, before and after radio-frequency glow discharge treatment for surface energy modification, illustrated the conditions for maximum attachment strength to nonphysiologic substances. Attachment to bony host parts was challenging but apparently met by the application of acrylic-composite-to-dentin bonding systems that has shown good long-term experience in the mouth. Above all, the compression-relaxation properties of the tape materials were superior and their uses in potential Nucleus Pulposus applications for spinal disc repair were most completely explored. Tests included tape-disc performance longevity, both dry and wet, for over 5000 load-relaxation cycles, with no apparent changes in results for the most dense of the tapes evaluated. Direct abrasion was avoided by insertion of rigid polymeric layers. It is recommended that the compressive loading properties of acrylic tapes be further evaluated for spine repair applications.

  15. UV curable polyester polyol acrylate/bentonite nanocomposites: synthesis, characterization, and drug release.

    PubMed

    Thatiparti, Thimma Reddy; Tammishetti, Shekharam; Nivasu, Muram V

    2010-01-01

    Polyesterpolyolacrylate/bentonite nanocomposites, capable of in situ photo polymerization, were synthesized and characterized. The organically modified bentonite clay was prepared by an ion exchange process, in which sodium ions were replaced by alkyl ammonium ions. Organo modification of bentonite was confirmed from X-ray diffraction and fourier transform-infrared data. Microstructures were characterized by XRD data and transmission electron microscopy (TEM). Both XRD data and TEM images of polyester polyol acrylate/organo modified bentonite nanocomposites indicated that most of silicate layers were intercalated into the acrylate matrix. The resulting nanocomposites were characterized by gel content, water equilibrium swell, tensile strength, and in vitro degradation. The results showed that water equilibrium swell and in vitro degradation of these nanocomposites decreased with increase in the clay content. The tensile strength of these nanocomposites also increased with increase in the clay content. Release of two model drugs namely sulfamethoxazole and diclofenac sodium (DS) from these nanocomposites was studied in phosphate buffer saline pH = 7.4 at 37 degrees C. The drug release studies showed that sulfamethoxazole released slower than DS from polyester polyol acrylate nanocomposites. Therefore, these materials may be useful for mucoadhesive drug carriers and other biomedical applications.

  16. Comparison of the long-term clinical results of hydrophilic and hydrophobic acrylic intraocular lenses.

    PubMed

    Suh, Youngwoo; Oh, Chunghoon; Kim, Hyo-Myung

    2005-03-01

    This study was performed to compare the incidence of posterior capsular opacity (PCO) and refractive errors between hydrophilic (ACR6D, Corneal) and hydrophobic (MA60BM, AcrySof) acrylic intraocular lenses (IOLs) over a 3-year follow-up after phacoemulsification surgery. The patients with AcrySof implanted in one eye and Corneal in the other eye were categorized as Group 1 (n=28), while those with one or both eyes implanted with IOLs of the same kind were categorized as Group 2 (AcrySof, n=90; Corneal, n=95). Refractive errors were evaluated at 3 months and 3 years postoperatively. The incidence of visually significant PCO was investigated 3 years postoperatively. Postoperative refractive values at 3 months were not significantly different between the two groups. However, refractive values at 3 years were significantly different between two IOLs in both groups [AcrySof -0.37+/-0.43D, Corneal -0.62+/-0.58D in Group 1 (p=0.04); AcrySof -0.38+/-0.52, Corneal -0.68+/-0.54 in Group 2 (p<0.01)]. The incidence of visually significant PCO was 14% and 32% in Group 1, and 13% and 28% in Group 2, for the AcrySof and Corneal implants, respectively. The incidence of visually significant PCO of hydrophilic acrylic IOLs was higher than that of hydrophobic acrylic IOLs in the 3-year follow-up. The postoperative 3-year refractive value of Corneal showed myopic shift.

  17. Effect of some curing methods on acrylic maxillary denture base fit.

    PubMed

    Ghani, Fazal; Kikuchi, Masahiko; Lynch, Christopher D; Watanabe, Makoto

    2010-09-01

    The aim of this study was to investigate the fit of acrylic maxillary denture bases processed by the methods of microwave, quick-wet-heat, slow-wet-heat, and self curing. Forty stone-casts were obtained using a mould of an undercut-free acrylic resin master cast of an edentulous maxilla. Standard acrylic replicas patterns sealed on casts and randomized to four groups (10 in each) were used to make denture bases using different processing methods for each of the four groups. The resultant discrepancy of fit between the denture base and the casts were measured using a silicone wafer. Varying fit discrepancies both within and between denture base groups was observed. The proportional fit-loss in the palatal region was significantly greater than the sulcular areas for all materials tested (p < 0.05). The fit-loss observed was greater in microwave-cured bases than for other materials examined. Careful selection of appropriate denture base materials and processing technique is important when providing complete dentures for edentulous patients.

  18. A liquid-film forming acrylate cream for the treatment of anal pruritus.

    PubMed

    Tomi, Nordwig; Weiser, Rudolf; Strohal, Robert; Mittlboeck, Martina

    Pruritus ani is a hidden but frequently occurring clinical condition, with a large impact on patients' quality of life. Currently, therapeutic options are scarce, offering mainly limited success. The authors performed a prospective, open-label, two-centre pilot study to analyse the efficacy and safety of a liquid-film forming acrylate cream for the treatment of pruritus ani and peri-anal skin irritation. A total of 28 patients were included and applied the cream to the cleansed anal and peri-anal skin once daily for a study period of 3-4 weeks. The primary outcome measure was the reduction of pruritis ani, comparing day 0 to day 28 results. For this purpose, a visual analog scale (VAS) was used. Secondary parameters included the physician global assessment score (PGA) of peri-anal skin condition, assessment of patients' quality of life using a specifically designed quality of life scoring tool, and patient satisfaction with the treatment regimen. The application of the acrylate skin protection cream resulted in a fast and substantial improvement of all study parameters, with a high score for patient satisfaction. The cream was well tolerated without any adverse events noted during the study period. The authors' pilot study has generated initial evidence that the acrylate skin protection cream may be effective for the treatment of pruritus ani. However, further randomized controlled studies are needed to confirm the authors' findings.

  19. Hydrophobic acrylic hard coating by surface segregation of hyper-branched polymers

    NASA Astrophysics Data System (ADS)

    Haraguchi, Masayuki; Hirai, Tomoyasu; Ozawa, Masaaki; Miyaji, Katsuaki; Tanaka, Keiji

    2013-02-01

    The ability of hyperbranched polymers (HBPs) to preferentially segregate to the surface of its matrix owing to its unique structure makes it a good candidate as a surface modifier. One particular challenge in its application as an efficient surface modifier, however, is its possible elimination from the surface due to the lack of attachments between a HBP (modifier) and its host material (polymer matrix). Here, we present a novel approach to efficiently prevent the removal of HBPs from the surface of its host material by directly reacting a HBP containing fluoroalkyl segments (F-HBP) to a multi-functional acrylate monomer prior to curing. We also have characterized surface structure and wettability of the acrylic hard coating material by X-ray photoelectron spectroscopic and contact angle measurements, respectively. The results show that since F-HBP was segregated at the surface, the surface became hydrophobic and more stable. Thus, we claim that our approach results in the formation of a water-repellent acrylic hard coating material.

  20. Thermal preparation of chitosan-acrylic acid superabsorbent: optimization, characteristic and water absorbency.

    PubMed

    Ge, Huacai; Wang, Senkang

    2014-11-26

    Chitosan-acrylic acid superabsorbent polymer was successfully prepared by the thermal reaction without using initiator and crosslinker in air. The effects of some reaction variables on the water absorbency of this polymer were investigated by orthogonal tests, and the optimal conditions were described. The influences of temperature, time, ratio of the reactants and neutralization degree of acrylic acid on the reaction were further studied. These polymers were also prepared in nitrogen atmosphere and by using a radical initiator and compared against thermal reaction obtained polymers. The structures of the polymers were characterized by FT-IR, TGA, XRD, (13)C NMR and elemental analyses. The results showed that the thermal reaction product of acrylic acid with chitosan might form N-carboxyethyl grafted and amide-linked polymer and this product could absorb water 644 times its own dry weight. The possible mechanism for the thermal reaction was further suggested. The purpose of this research was to explore the friendly synthesized method of the superabsorbent.

  1. Dimensional Changes of Acrylic Resin Denture Bases: Conventional Versus Injection-Molding Technique

    PubMed Central

    Gharechahi, Jafar; Asadzadeh, Nafiseh; Shahabian, Foad; Gharechahi, Maryam

    2014-01-01

    Objective: Acrylic resin denture bases undergo dimensional changes during polymerization. Injection molding techniques are reported to reduce these changes and thereby improve physical properties of denture bases. The aim of this study was to compare dimensional changes of specimens processed by conventional and injection-molding techniques. Materials and Methods: SR-Ivocap Triplex Hot resin was used for conventional pressure-packed and SR-Ivocap High Impact was used for injection-molding techniques. After processing, all the specimens were stored in distilled water at room temperature until measured. For dimensional accuracy evaluation, measurements were recorded at 24-hour, 48-hour and 12-day intervals using a digital caliper with an accuracy of 0.01 mm. Statistical analysis was carried out by SPSS (SPSS Inc., Chicago, IL, USA) using t-test and repeated-measures ANOVA. Statistical significance was defined at P<0.05. Results: After each water storage period, the acrylic specimens produced by injection exhibited less dimensional changes compared to those produced by the conventional technique. Curing shrinkage was compensated by water sorption with an increase in water storage time decreasing dimensional changes. Conclusion: Within the limitations of this study, dimensional changes of acrylic resin specimens were influenced by the molding technique used and SR-Ivocap injection procedure exhibited higher dimensional accuracy compared to conventional molding. PMID:25584050

  2. Effect of Nanosilver on Thermal and Mechanical Properties of Acrylic Base Complete Dentures

    PubMed Central

    Hamedi-Rad, Fahimeh; Ghaffari, Tahereh; Rezaii, Farzad; Ramazani, Ali

    2014-01-01

    Objective: Polymethyl methacrylate (PMMA), widely used as a prosthodontic base, has many disadvantages, including a high thermal expansion coefficient and low thermal conductivity, a low elasticity coefficient, low impact strength and low resistance to fatigue. This study aimed to make an in vitro comparison of the thermal conductivity, compressive strength, and tensile strength of the acrylic base of complete dentures with those of acrylic reinforced with nanosilver. Materials and Methods: For this study, 36 specimens were prepared. The specimens were divided into three groups of 12; which were further divided into two subgroups of control (unmodified PMMA) and test (PMMA mixed with 5 weight% nanosilver).The results were analysed by Independent t-test. Results: This study showed that the mean thermal conductivity and compressive strength of PMMA reinforced with nanosilver were significantly higher than the unmodified PMMA (P<0.05), while the tensile strength decreased significantly after the incorporation of nanosilver (P<0.05). Conclusion: Considering our results suggesting the favorable effect of silver nanoparticles on improving the thermal conductivity and compressive strength of PMMA, use of this material in the palatal area of maxillary acrylic resin dentures is recommended. PMID:25628675

  3. Effect of Antiadherents on the Physical and Drug Release Properties of Acrylic Polymeric Films.

    PubMed

    Ammar, Hussein O; Ghorab, Mamdouh M; Felton, Linda A; Gad, Shadeed; Fouly, Aya A

    2016-06-01

    Antiadherents are used to decrease tackiness of a polymer coating during both processing and subsequent storage. Despite being a common excipient in coating formulae, antiadherents may affect mechanical properties of the coating film as well as drug release from film-coated tablets, but how could addition of antiadherents affect these properties and to what extent and is there a relation between the physical characteristics of the tablet coat and the drug release mechanisms? The aim of this study was to evaluate physical characteristics of films containing different amounts of the antiadherents talc, glyceryl monostearate, and PlasACRYL(TM) T20. Eudragit RL30D and Eudragit RS30D as sustained release polymers and Eudragit FS30D as a delayed release material were used. Polymer films were characterized by tensile testing, differential scanning calorimetry (DSC), microscopic examination, and water content as calculated from loss on drying. The effect of antiadherents on in vitro drug release for the model acetylsalicylic acid tablets coated with Eudragit FS30D was also determined. Increasing talc concentration was found to decrease the ability of the polymer films to resist mechanical stress. In contrast, glyceryl monostearate (GMS) and PlasACRYL produced more elastic films. Talc at concentrations higher than 25% caused negative effects, which make 25% concentration recommended to be used with acrylic polymers. All antiadherents delayed the drug release at all coating levels; hence, different tailoring of drug release may be achieved by adjusting antiadherent concentration with coating level.

  4. Silver nanoparticle incorporation effect on mechanical and thermal properties of denture base acrylic resins

    PubMed Central

    KÖROĞLU, Ayşegül; ŞAHİN, Onur; KÜRKÇÜOĞLU, Işın; DEDE, Doğu Ömür; ÖZDEMİR, Tonguç; HAZER, Baki

    2016-01-01

    ABSTRACT Objective The aim of the present study was to evaluate the mechanical and thermal characteristics of two denture base acrylic resins containing silver nanoparticles (AgNPs). Material and Methods Two different acrylic denture base resins (heat-polymerized and microwave polymerized) containing 0.3, 0.8 and 1.6 wt% AgNPs were evaluated for flexural strength, elastic modulus and impact strength. The glass transition temperature (Tg) and relative heat capacity (Cp) of the samples were determined from the Differential Scanning Calorimetry (DSC) results. For statistical analysis, two-way ANOVA and Tukey-HSD tests were performed. Results Addition of 0.8% and 1.6% AgNPs in microwave-polymerized resin significantly decreased the transverse strength and elastic modulus. In terms of impact strength, the addition of AgNPs has no effect on both resin groups. Glass transition temperature (Tg) was decreased with the addition of AgNPs for both denture base resins. Conclusions The incorporation of AgNPs, generally used for antimicrobial efficiency, affected the transverse strength of the denture base acrylic resins depending on the concentration of nanoparticles. Tg was decreased with the addition of AgNPs for both denture base resins. PMID:28076464

  5. A Potentiometric Formaldehyde Biosensor Based on Immobilization of Alcohol Oxidase on Acryloxysuccinimide-modified Acrylic Microspheres

    PubMed Central

    Ling, Yew Pei; Heng, Lee Yook

    2010-01-01

    A new alcohol oxidase (AOX) enzyme-based formaldehyde biosensor based on acrylic microspheres has been developed. Hydrophobic poly(n-butyl acrylate-N-acryloxy-succinimide) [poly(nBA-NAS)] microspheres, an enzyme immobilization matrix, was synthesized using photopolymerization in an emulsion form. AOX-poly(nBA-NAS) microspheres were deposited on a pH transducer made from a layer of photocured and self-plasticized polyacrylate membrane with an entrapped pH ionophore coated on a Ag/AgCl screen printed electrode (SPE). Oxidation of formaldehyde by the immobilized AOX resulted in the production of protons, which can be determined via the pH transducer. Effects of buffer concentrations, pH and different amount of immobilization matrix towards the biosensor’s analytical performance were investigated. The formaldehyde biosensor exhibited a dynamic linear response range to formaldehyde from 0.3–316.2 mM and a sensitivity of 59.41 ± 0.66 mV/decade (R2 = 0.9776, n = 3). The lower detection limit of the biosensor was 0.3 mM, while reproducibility and repeatability were 3.16% RSD (relative standard deviation) and 1.11% RSD, respectively (n = 3). The use of acrylic microspheres in the potentiometric formaldehyde biosensor improved the biosensor’s performance in terms of response time, linear response range and long term stability when compared with thick film immobilization methods. PMID:22163450

  6. Rehabilitation of post-traumatic total nasal defect using silicone and acrylic resin

    PubMed Central

    Aggarwal, Vikas; Datta, Kusum; Kaur, Sukhjit

    2016-01-01

    Facial defects resulting from neoplasms, congenital abnormalities or trauma can affect the patient esthetically, psychologically, and even financially. Surgical reconstruction of large facial defects is sometimes not possible and frequently demands prosthetic rehabilitation. For success of such prosthesis, adequate replication of natural anatomy, color matching and blending with tissue interface are important criteria. Variety of materials and retention methods are advocated to achieve a functionally and esthetically acceptable restoration. Silicones are the most commonly used materials because of flexibility, lifelike appearance and ability to be used in combination with acrylic resin which is hard, provides body and helps in achieving retention to the prosthesis by engaging mechanical undercuts. Furthermore, the acrylic portion can be relined easily, thus helping comfortable wear and removal of the prosthesis by patient without traumatizing nasal mucosa. This case report describes time saving and cost effective prosthetic rehabilitation of a patient with total nasal defect using custom sculpted nasal prosthesis made up of silicone elastomer and acrylic resin, which is retained by engaging mechanical undercut and use of biocompatible silicone adhesive. PMID:27134434

  7. Waterborne polyurethane-acrylic hybrid nanoparticles by miniemulsion polymerization: applications in pressure-sensitive adhesives.

    PubMed

    Lopez, Aitziber; Degrandi-Contraires, Elise; Canetta, Elisabetta; Creton, Costantino; Keddie, Joseph L; Asua, José M

    2011-04-05

    Waterborne polyurethane-acrylic hybrid nanoparticles for application as pressure-sensitive adhesives (PSAs) were prepared by one-step miniemulsion polymerization. The addition of polyurethane to a standard waterborne acrylic formulation results in a large increase in the cohesive strength and hence a much higher shear holding time (greater than seven weeks at room temperature), which is a very desirable characteristic for PSAs. However, with the increase in cohesion, there is a decrease in the relative viscous component, and hence there is a decrease in the tack energy. The presence of a small concentration of methyl methacrylate (MMA) in the acrylic copolymer led to phase separation within the particles and created a hemispherical morphology. The tack energy was particularly low in the hybrid containing MMA because of the effects of lower energy dissipation and greater cross-linking. These results highlight the great sensitivity of the viscoelastic and adhesive properties to the details of the polymer network architecture and hence to the precise composition and synthesis conditions.

  8. Cross-linked acrylic hydrogel for the controlled delivery of hydrophobic drugs in cancer therapy

    PubMed Central

    Deepa, G; Thulasidasan, Arun Kumar T; Anto, Ruby John; Pillai, J Jisha; Kumar, GS Vinod

    2012-01-01

    Objective: To investigate cross-linked hydrogels prepared via inverse emulsion polymerization to entrap poorly aqueous soluble drugs. Polyethylene glycol cross-linked acrylic polymers were synthesized and the loading and release of curcumin, a model hydrophobic drug, was investigated. Methods: Physicochemical characteristics of hydrogels were studied with 13C nuclear magnetic resonance, Fourier transform infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, differential scanning calorimetry, and swelling. Polymerization of the acrylic acid with cross-linked polyethylene glycol diacrylate was characterized with 13C nuclear magnetic resonance imaging and Fourier transform infrared spectroscopy. Results: The in vitro release rate of curcumin showed that there was a sustained release from the hydrogel with increased cross-linking; the release rate depended on the pH of the releasing medium. Intracellular and cytotoxicity studies were carried out in human cervical cancer cell lines. Conclusion: The results suggest cross-linked acrylic polymers can be used as efficient vectors for pH-sensitive, controlled delivery of hydrophobic drugs. PMID:22888244

  9. Thermodynamic Interactions between Polystyrene and Long-Chain Poly(n-Alkyl Acrylates) Derived from Plant Oils.

    PubMed

    Wang, Shu; Robertson, Megan L

    2015-06-10

    Vegetable oils and their fatty acids are promising sources for the derivation of polymers. Long-chain poly(n-alkyl acrylates) and poly(n-alkyl methacrylates) are readily derived from fatty acids through conversion of the carboxylic acid end-group to an acrylate or methacrylate group. The resulting polymers contain long alkyl side-chains with around 10-22 carbon atoms. Regardless of the monomer source, the presence of alkyl side-chains in poly(n-alkyl acrylates) and poly(n-alkyl methacrylates) provides a convenient mechanism for tuning their physical properties. The development of structured multicomponent materials, including block copolymers and blends, containing poly(n-alkyl acrylates) and poly(n-alkyl methacrylates) requires knowledge of the thermodynamic interactions governing their self-assembly, typically described by the Flory-Huggins interaction parameter χ. We have investigated the χ parameter between polystyrene and long-chain poly(n-alkyl acrylate) homopolymers and copolymers: specifically we have included poly(stearyl acrylate), poly(lauryl acrylate), and their random copolymers. Lauryl and stearyl acrylate were chosen as model alkyl acrylates derived from vegetable oils and have alkyl side-chain lengths of 12 and 18 carbon atoms, respectively. Polystyrene is included in this study as a model petroleum-sourced polymer, which has wide applicability in commercially relevant multicomponent polymeric materials. Two independent methods were employed to measure the χ parameter: cloud point measurements on binary blends and characterization of the order-disorder transition of triblock copolymers, which were in relatively good agreement with one another. The χ parameter was found to be independent of the alkyl side-chain length (n) for large values of n (i.e., n > 10). This behavior is in stark contrast to the n-dependence of the χ parameter predicted from solubility parameter theory. Our study complements prior work investigating the interactions between

  10. Development and characterization of amorphous acrylate networks for use as switchable adhesives inspired from shapememory behavior

    NASA Astrophysics Data System (ADS)

    Lakhera, Nishant

    Several types of insects and animals such as spiders and geckos are inherently able to climb along vertical walls and ceilings. This remarkable switchable adhesive behavior has been attributed to the fibrillar structures on their feet, with size ranging from few nanometers to a few micrometers depending on the species. Several studies have attempted to create synthetic micro-patterned surfaces trying to imitate this adhesive behavior seen in nature. The experimental procedures are scattered, with sole purpose of trying to increase adhesion, thereby making direct comparison between studies very difficult. There is a lack of fundamental understanding on adhesion of patterned surfaces. The influence of critical parameters like material modulus, glass transition temperature, viscoelastic effects, temperature and water absorption on adhesion is not fully explored and characterized. These parameters are expected to have a decisive influence on adhesion behavior of the polymer. Previous studies have utilized conventional "off-the-shelf" materials like epoxy, polyurethanes etc. It is however, impossible to change the material modulus, glass transition temperature etc. of these polymer systems without changing the base constituents itself, thereby explaining the gaps in the current research landscape. The purpose of this study was to use acrylate shape-memory polymers (SMPs) for their ability to be tailored to specific mechanical properties by control of polymer chemistry, without changing the base constituents. Polymer networks with tailorable glass transition, material modulus, water absorption etc. were developed and adhesion studies were performed to investigate the influence of temperature, viscoelastic effects, material modulus on the adhesion behavior of flat acrylate polymer surfaces. The knowledge base gained from these studies was utilized to better understand the fundamental mechanisms associated with adhesion behavior of patterned acrylate surfaces. Thermally

  11. Metabolism of acrylate to {beta}-hydroxypropionate and its role in dimethylsulfoniopropionate lyase induction by a salt marsh sediment bacterium, Alcaligenes faecalis M3A

    SciTech Connect

    Ansede, J.H.; Pellechia, P.J.; Yoch, D.C.

    1999-11-01

    Dimethylsulfoniopropionate (DMSP) is degraded to dimethylsulfide (DMS) and acrylate by the enzyme DMSP lyase. DMS or acrylate can serve as a carbon source for both free-living and endophytic bacteria in the marine environment. In this study, the authors report on the mechanism of DMSP-acrylate metabolism by Alcaligenes faecalis M3A. Suspensions of citrate-grown cells expressed a low level of DMSP lyase activity that could be induced to much higher levels in the presence of DMSP, acrylate, and its metabolic product, {beta}-hydroxypropionate. DMSP was degraded outside the cell, resulting in an extracellular accumulation of acrylate, which in suspensions of citrate-grown cells was then metabolized at a low endogenous rate. The inducible nature of acrylate metabolism was evidenced by both an increase in the rate of its degradation over time and the ability of acrylate-grown cells to metabolize this molecule at about an eight times higher rate than citrate-grown cells. Therefore, acrylate induces both its production (from DMSP) and its degradation by an acrylase enzyme. {sup 1}H and {sup 13}C nuclear magnetic resonance analyses were used to identify the products resulting from [1-{sup 13}C]acrylate metabolism. The results indicated that A.faecalis first metabolized acrylate to {beta}-hydroxypropionate outside the cell, which was followed by its intracellular accumulation and subsequent induction of DMSP lyase activity. In summary, the mechanism of DMSP degradation to acrylate and the subsequent degradation of acrylate to {beta}-hydroxypropionate in the aerobic {beta}-Proteobacterium A.faecalis has been described.

  12. Is the bond between acrylic resin denture teeth and denture base resin stronger if they are both made by the same manufacturer?

    PubMed

    Patil, Reshma; Juszczyk, Andrzej S; Radford, David R; Clark, Robert K F

    2010-03-01

    A previous study suggested that a stronger bond may be achieved between acrylic resin denture base material and acrylic denture teeth when both are made by the same manufacturer. Three denture base acrylic resins from three different manufacturers were bonded to three different acrylic resin denture teeth, one of which was manufactured by each of the manufacturers of the base material. In each group there was a trend that the bond strength achieved between the teeth and base material from the same manufacturer was higher than the unmatched pairs but statistical significance was not achieved.

  13. Effect of various chemicals on the bond strength of acrylic tooth and denture base -An Invitro comparative study

    PubMed Central

    Krishna, V Pridhvi; Premalatha, Averneni; Babu, P Jithendra; Raju, D Srinivasa; Kumar, M Praveen; Rao, D Bheemalingeswara

    2014-01-01

    Background: Debonding of acrylic teeth from the denture base is a common problem. Certain clinical conditions like ridge prominence leads to excess trimming of acrylic teeth and base, resulting in a weak interface. The denture base polymer debonds adhesively in the region of the highly cross –linked matrix of the teeth. To compare the effect of different chemical surface treatments on the bond between cross-linked acrylic teeth and different types of denture base material. Materials & Methods: A total of 180 wax specimens were fabricated and divided into 3 groups: Heat-cure, high impact heat-cure, flexible denture base material bonded to acrylic teeth. Each group was further subdivided into 6 subgroups with 10 specimens each according to the surface treatment ofthe ridge lap area: control, monomer, acetone 99%, chloroform 99%, acrylic adhesive cyanoacrylate, ethyl acetate 99%. After processing, specimens were tested for bond strength using a universal testing machine. The resulting bond strengths were recorded, statistically analyzed and compared. Results: Among all the 3types of denture base resins, highimpact heat-cure denture base resin gave highest bond strength. There was no bonding of teeth with flexible denture base material. Chemical surface treatment of acrylic teeth with ethyl acetate gave highest bond strength followed by control, chloroform, acetone and cyanoacrylate groups. Conclusion: Among all the 3types of denture base materials, high-impact heat-cure denture base resin gave highest bond strength with ethyl acetate surface treatment. Simple and quick tooth chemical surface treatment with ethylacetate could be an effective option in decreasing bonding failures and also avoid repeated denture repairs improving patient satisfaction. How to cite the article: Krishna VP, Premalatha A, Babu PJ, Raju DS, Kumar MP, Rao DB. Effect of various chemicals on the bond strength of acrylic tooth and denture base -An In-vitro comparative study. J Int Oral Health

  14. Designing Visible Light-Cured Thiol-Acrylate Hydrogels for Studying the HIPPO Pathway Activation in Hepatocellular Carcinoma Cells.

    PubMed

    Lin, Tsai-Yu; Bragg, John C; Lin, Chien-Chi

    2016-04-01

    Various polymerization mechanisms have been developed to prepare peptide-immobilized poly(ethylene glycol) (PEG) hydrogels, a class of biomaterials suitable for studying cell biology in vitro. Here, a visible light mediated thiol-acrylate photopolymerization scheme is reported to synthesize dually degradable PEG-peptide hydrogels with controllable crosslinking and degradability. The influence of immobilized monothiol pendant peptide is systematically evaluated on the crosslinking of these hydrogels. Further, methods are proposed to modulate hydrogel crosslinking, including adjusting concentration of comonomer or altering the design of multifunctional peptide crosslinker. Due to the formation of thioether ester bonds, these hydrogels are hydrolytically degradable. If the dithiol peptide linkers used are susceptible to protease cleavage, these thiol-acrylate hydrogels can be designed to undergo partial proteolysis. The differences between linear and multiarm PEG-acrylate (i.e., PEGDA vs PEG4A) are also evaluated. Finally, the use of the mixed-mode thiol-acrylate PEG4A-peptide hydrogels is explored for in situ encapsulation of hepatocellular carcinoma cells (Huh7). The effects of matrix stiffness and integrin binding motif (e.g., RGDS) on Huh7 cell growth and HIPPO pathway activation are studied using PEG4A-peptide hydrogels. This visible light poly-merized thiol-acrylate hydrogel system represents an alternative to existing light-cured hydrogel platforms and shall be useful in many biomedical applications.

  15. The effect of additives and mechanical agitation in surface modification of acrylic fibres by cutinase and esterase.

    PubMed

    Matamá, Teresa; Vaz, Filipe; Gübitz, Georg M; Cavaco-Paulo, Artur

    2006-01-01

    The surface of an acrylic fibre containing about 7% of vinyl acetate was modified using Fusarium solani pisi cutinase and a commercial esterase, Texazym PES. The effect of acrylic solvents and stabilising polyols on cutinase operational stability was studied. The half-life time of cutinase increased by 3.5-fold with the addition of 15% N,N-dimethylacetamide (DMA) and by 3-fold with 1M glycerol. The impact of additives and mechanical agitation in the protein adsorption and in the hydrolysis of vinyl acetate from acrylic fabric was investigated. The hydroxyl groups produced on the surface of the fibre were able to react specifically with Remazol Brilliant Blue R (cotton reactive dye) and to increase the colour of the acrylic-treated fabric. The best staining level was obtained with a high level of mechanical agitation and with the addition of 1% DMA. Under these conditions, the raise in the acrylic fabric colour depth was 30% for cutinase and 25% for Texazym. The crystallinity degree, determined by X-ray diffraction, was not significantly changed between control samples and samples treated with cutinase. The results showed that the outcome of the application of these enzymes depends closely on the reaction media conditions.

  16. Radiation synthesis of eco-friendly water reducing sulfonated starch/acrylic acid hydrogel designed for cement industry

    NASA Astrophysics Data System (ADS)

    Abd El-Rehim, H. A.; Hegazy, El-Sayed A.; Diaa, D. A.

    2013-04-01

    Starch was treated with chlorosulfonic acid to obtain sulfonated starch. Acrylic acid/sulfonated starch semi-interpenetrated network IPN of different compositions was prepared using ionizing radiation. Swelling of prepared IPNs at different environmental conditions was studied. The possible use of sulfonated starch/acrylic acid IPN as a water-retarding agent in the cement industry was investigated. ζ-potential measurements were used to determine the stability of the colloidal cement—SS/AA and cement -poly-naphthalene sulfonic acid (SNF) water retarding mixtures. Sulfonated starch/acrylic acid water-retarding property was influenced by hydrogel concentration and composition. Sulfonated starch/acrylic acid IPN admixture has a great effect on the cement initial setting time. Using 2% of SS/AA or SNF resulted in an increase in initial setting time by 2 and 1 h respectively, if compared with native cement initial setting time. The results showed that the synthetic commercial super-plasticizers could be replaced by an eco-friendly water-retarding sulfonated starch/acrylic acid IPN in the cement industry.

  17. Anti-fouling ultrafiltration membrane prepared from polysulfone-graft-methyl acrylate copolymers by UV-induced grafting method.

    PubMed

    Hua, Helin; Li, Na; Wu, Linlin; Zhong, Hui; Wu, Guangxial; Yuan, Zonghuan; Lin, Xiangwei; Tang, Lianyi

    2008-01-01

    Membrane fouling is one of the most important challenges faced in membrane ultrafiltration operations. The copolymers of polysulfone-graft-methyl acrylate were synthesized by homogeneous photo-initiated graft copolymerization. The variables affecting the degree of grafting, such as the time of UV (Ultraviolet-visible) irradiation and the concentrations of the methyl acrylate and photoinitiator, were investigated. The graft copolymer membranes were prepared by the phase inversion method. The chemical and morphological changes were characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR/FT-IR), scanning electron microscopy, and water contact angles measurements. Results revealed that methyl acrylate groups were present on the membranes and the graft degree of methyl acrylate had remarkable effect on the performance of membranes. Pure water contact angle on the membrane surface decreases with the increase of methyl acrylate graft degree, which indicated that the hydrophilicity of graft copolymer membranes was improved. The permeation fluxes of pure water and bovine serum albumin solution were measured to evaluate the antifouling property of graft copolymer membranes, the results of which have shown an enhancement of antifouling property for graft copolymer membranes.

  18. Tuning of thermally induced sol-to-gel transitions of moderately concentrated aqueous solutions of doubly thermosensitive hydrophilic diblock copolymers poly(methoxytri(ethylene glycol) acrylate)-b-poly(ethoxydi(ethylene glycol) acrylate-co-acrylic acid).

    PubMed

    Jin, Naixiong; Zhang, Hao; Jin, Shi; Dadmun, Mark D; Zhao, Bin

    2012-03-15

    We report in this article a method to tune the sol-to-gel transitions of moderately concentrated aqueous solutions of doubly thermosensitive hydrophilic diblock copolymers that consist of two blocks exhibiting distinct lower critical solution temperatures (LCSTs) in water. A small amount of weak acid groups is statistically incorporated into the lower LCST block so that its LCST can be tuned by varying solution pH. Well-defined diblock copolymers, poly(methoxytri(ethylene glycol) acrylate)-b-poly(ethoxydi(ethylene glycol) acrylate-co-acrylic acid) (PTEGMA-b-P(DEGEA-co-AA)), were prepared by reversible addition-fragmentation chain transfer polymerization and postpolymerization modification. PTEGMA and PDEGEA are thermosensitive water-soluble polymers with LCSTs of 58 and 9 °C, respectively, in water. A 25 wt % aqueous solution of PTEGMA-b-P(DEGEA-co-AA) with a molar ratio of DEGEA to AA units of 100:5.2 at pH = 3.24 underwent multiple phase transitions upon heating, from a clear, free-flowing liquid (<15 °C) to a clear, free-standing gel (15-46 °C) to a clear, free-flowing hot liquid (47-56 °C), and a cloudy mixture (≥57 °C). With the increase of pH, the sol-to-gel transition temperature (T(sol-gel)) shifted to higher values, while the gel-to-sol transition (T(gel-sol)) and the clouding temperature (T(clouding)) of the sample remained essentially the same. These transitions and the tunability of T(sol-gel) originated from the thermosensitive properties of two blocks of the diblock copolymer and the pH dependence of the LCST of P(DEGEA-co-AA), which were confirmed by dynamic light scattering and differential scanning calorimetry studies. Using the vial inversion test method, we mapped out the C-shaped sol-gel phase diagrams of the diblock copolymer in aqueous buffers in the moderate concentration range at three different pH values (3.24, 5.58, and 5.82, all measured at ~0 °C). While the upper temperature boundaries overlapped, the lower temperature boundary

  19. Matrix normalized MALDI-TOF quantification of a fluorotelomer-based acrylate polymer.

    PubMed

    Rankin, Keegan; Mabury, Scott A

    2015-05-19

    The degradation of fluorotelomer-based acrylate polymers (FTACPs) has been hypothesized to serve as a source of the environmental contaminants, perfluoroalkyl carboxylates (PFCAs). Studies have relied on indirect measurement of presumed degradation products to evaluate the environmental fate of FTACPs; however, this approach leaves a degree of uncertainty. The present study describes the development of a quantitative matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry method as the first direct analysis method for FTACPs. The model FTACP used in this study was poly(8:2 FTAC-co-HDA), a copolymer of 8:2 fluorotelomer acrylate (8:2 FTAC) and hexadecyl acrylate (HDA). Instead of relying on an internal standard polymer, the intensities of 40 poly(8:2 FTAC-co-HDA) signals (911-4612 Da) were normalized to the signal intensity of a matrix-sodium cluster (659 Da). We termed this value the normalized polymer response (P(N)). By using the same dithranol solution for the sample preparation of poly(8:2 FTAC-co-HDA) standards, calibration curves with coefficient of determinations (R(2)) typically >0.98 were produced. When poly(8:2 FTAC-co-HDA) samples were prepared with the same dithranol solution as the poly(8:2 FTAC-co-HDA) standards, quantification to within 25% of the theoretical concentration was achieved. This approach minimized the sample-to-sample variability that typically plagues MALDI-TOF, and is the first method developed to directly quantify FTACPs.

  20. Adherence of Candida albicans to glow-discharge modified acrylic denture base polymers.

    PubMed

    Yildirim, M S; Hasanreisoglu, U; Hasirci, N; Sultan, N

    2005-07-01

    An important aetiologic factor in the pathogenesis of denture-induced stomatitis, is the presence of numerous yeasts, usually Candida albicans, on the fitting surfaces of dentures. In the present study, effect of glow-discharge plasma, a technique applied to increase surface wettability of acrylic resins, on candidial adherence was evaluated. The durability of glow-discharge modification with saliva coating was also evaluated. Samples including control and experimental groups were prepared by using heat compression mould technique. To create a hydrophobicity gradient, experimental groups were exposed to a radiofrequency glow discharge in an O2 atmosphere under different discharge powers. To characterize the wetting properties, an expression of surface hydrophobicity, contact angle measurements were performed by the sessile drop method. The organism used was C. albicans (ATTC10321). Acrylic samples were coated with unstimulated whole saliva collected from a healthy man. The fungal suspension was poured on saliva-inoculated samples and incubated at 37 degrees for 2 h. The samples were then fixed with glutaraldehyde and Gram stained. Adhered candidial cells were examined by light microscope. Diffuse Reflectance FTIR (DRIFT) and scanning electron-microscope examinations were also performed to evaluate the surface composition and roughness of the test groups. Glow-discharge plasma was found to be an effective means of increasing surface wettability even with salivary pellicle. Amounts of candida cells adhered were significantly higher in all the plasma treated surfaces than the unmodified control group (P < 0.001). It was concluded that improving the surface wettability of acrylic resins by glow-discharge plasma in O2 atmosphere increased the adherence of the C. albicans.