Hydrolysis and stability of thin pulsed plasma polymerised maleic anhydride coatings

DEFF Research Database (Denmark)

Drews, Joanna Maria; Launay, Héléne; Hansen, Charles M.

2008-01-01

Abstract The stability of plasma polymerised layers has become important because of their widespread use. This study explored the hydrolysis and degradation stability of coatings of plasma polymerised maleic anhydride. Coatings made with different plasma parameters were exposed to aqueous media...... of different pH as a function of time. ATR-FTIR was used for structure analysis and a toluidine blue staining method allowed quantitative analysis of the hydrolysis of anhydride groups to acid groups. Coatings with constant thickness were obtained at different plasma powers and layers with varying thickness...

Synthesis and thermal characterization of CdS nano crystals in previously formed template of maleic anhydride-octene 1-vinyl butyl terpolymer

International Nuclear Information System (INIS)

Akbarov, O.H; Mammadova, R.E; Malikov, E.Y.

2008-01-01

Full text: Nano crystals have dimensions in the range 10100 nm. Crystals in this size range possess unique properties, which enable scientists to manufacture materials and devices capable of performing unimaginable tasks. For that reason synthesis of this semiconductor nano crystals is expedient. Many useful methods have been used for preparing sulphide semiconductor nano crystals, such as colloidal chemistry method, sol-gel method, inverse micelle method, in situ synthesis and assemble on polymer template. The most significant method is in situ synthesis and assemble of sulphide semiconductor nano crystals on polymer. Compared with other methods, the stability of nanoparticles is improved by the protection and confinement of the copolymer. Because of confinement and protection effects of template environmental risk is prevented in this method. On the base of this principles in situ synthesis of CdS nano crystals in maleic anhydride-octene 1-vinyl butyl terpolymer was realized in this scientific work. First of all in specific condition maleic anhydride, octene 1, and vinyl butyl ether were polymerized to form a terpolymer as the result of radical ter polymerization. In second step CdS nano crystals were synthesized in N,N-dimethylformamide solution of maleic anhydride-octene 1-vinyl butyl terpolymer through the reaction of thiourea with cadmium chloride. In this process CdCI 2 x 2.5H 2 O was dissolved in N,N-dimethylformamide solution of previously formed terpolymer and was heated in 90 0 C temperature for 4 hours with vigorous stirring. Then desired amount of thiourea in N,N-dimethylformamide was quickly injected into the reaction flask using a syringe. The reaction continued for another 1 hour, and a yellow clear solution was obtained, which indicated the formation of CdS nano crystals

Urea- Hydrogen Peroxide (UHP Oxidation of Thiols to the Corresponding Disulfides Promoted by Maleic Anhydride as Mediator

Directory of Open Access Journals (Sweden)

M. H. Habibi

2005-10-01

Full Text Available Urea-hydrogen peroxide (UHP was used in the presence of maleic anhydride as mediator in a simple and convenient method for the oxidation in high yield of some thiols to the corresponding disulfides. Peroxymaleic acid formed in situ from the reaction of UHP with maleic anhydride has a key role in this oxidation. Performance of the reaction in various solvents showed that methanol was the solvent of choice at 0 oC. The products were isolated by simple filtration on silica gel.

THE GRAFTING OF MALEIC-ANHYDRIDE ON HIGH-DENSITY POLYETHYLENE IN AN EXTRUDER

NARCIS (Netherlands)

GANZEVELD, KJ; JANSSEN, LPBM

The grafting of maleic anhydride (MAH) on high density polyethylene in a counter-rotating twin screw extruder has been studied. As the reaction kinetics appear to be affected by mass transfer, good micro mixing in the extruder is important. Due to the competing mechanisms of increasing mixing and

Grafting amino drugs to poly(styrene-alt-maleic anhydride) as a potential method for drug release

Energy Technology Data Exchange (ETDEWEB)

Khazaei, Ardeshir; Saednia, Shahnaz; Saien, Javad; Abbasi, Fatemeh, E-mail: Khazaei_1326@yahoo.com, E-mail: ssaednia@gmail.com [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of); Kazem-Rostami, Masoud [Young Researchers Club and Elite, Takestan Branch, Islamic Azad University, Takestan (Iran, Islamic Republic of); Sadeghpour, Mahdieh [Department of Chemistry, Takestan Branch, Islamic Azad University, Takestan (Iran, Islamic Republic of); Borazjani, Maryam Kiani [Faculty of Science, Department of Chemistry, Bushehr Payame Noor University (PNU), Bushehr (Iran, Islamic Republic of)

2013-07-15

Drug delivery systems based on polymer-drug conjugates give an improved treatment with lower toxicity or side effects and be used for the treatment of different diseases. Conjugates of biodegradable poly(styrene-alt-maleic anhydride) (PSMA), with a therapeutic agents such as amantadine hydrochloride, amlodipine, gabapentin, zonisamide and mesalamine, were afforded by the formation of the amide bonds of the amino drugs that reacted with the PSMA anhydride groups. The amounts of covalently conjugated drugs were determined by a {sup 1}H NMR spectroscopic method, and the in vitro release rate in buffer solution (pH 1.3) was studied at body temperature 37 Degree-Sign C. In kinetic studies, different dissolution models were examined to obtain drug release data and the collected data were well-fitted to the Korsmeyer-Peppas equation, revealing a dominant Fickian diffusion mechanism for drug release under the in vitro conditions. (author)

Réaction du polyisobutène chloré sur l'anhydride maléique : mécanisme. Catalyse par l'anhydride dichloromaléique Reaction of Chlorinated Polyisobutene on Maleic Anhydride. Mechanism. Catalysis by Dichloromaleic Anhydride

Directory of Open Access Journals (Sweden)

Sillion B.

2006-11-01

Full Text Available Dans cet article le mécanisme de la réaction de condensation du polyisobutène chloré sur l'anhydride maléique, qui sert dans la synthèse d'additif pour lubrifiant, est étudié par une cinétique globale et par un travail sur composés modèles. Il est montré que, dans cette réaction, l'anhydride maléique joue un double rôle : de catalyseur de déshydrochloration par une réactivité de type acide de Lewis organique, de réactif comme diénophile. Grâce à ces résultats, il est proposé une catalyse par l'anhydride dichloromaléique, qui permet une amélioration sensible du procédé. This article examines the mechanism of the chlorinated-polyisobutene condensation reaction on maleic anhydride. The overall kinetics and model compounds are investigated for this reaction which is used in the synthesis of lubricant additives. Maleic anhydride is shown to play the dual role of a dehydrochlorination catalyst by having a reactivity of the organic Lewis acid type and of a reactant like dienophile. These results are used to propose a catalysis by dichloromaleic anhydride which appreciably improves the process.

Amphiphilic poly{[α-maleic anhydride-ω-methoxypoly(ethylene glycol]-co-(ethyl cyanoacrylate} graft copolymer nanoparticles as carriers for transdermal drug delivery

Directory of Open Access Journals (Sweden)

Jinfeng Xing

2009-10-01

Full Text Available Jinfeng Xing, Liandong Deng, Jun Li, Anjie DongDepartment of Polymer Science and Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, People’s Republic of ChinaAbstract: In this study, the transdermal drug delivery properties of D,L-tetrahydropalmatine (THP-loaded amphiphilic poly{[α-maleic anhydride-ω-methoxy-poly(ethylene glycol]-co-(ethyl cyanoacrylate} (PEGECA graft copolymer nanoparticles (PEGECAT NPs were evaluated by skin penetration experiments in vitro. The transdermal permeation experiments in vitro were carried out in Franz diffusion cells using THP-loaded PEGECAT NPs as the donor system. Transmission electron microscopy and Fourier transform infrared spectroscopy were used to characterize the receptor fluid. The results indicate that the THP-loaded PEGECAT NPs are able to penetrate the rat skin. Fluorescent microscopy measurements demonstrate that THP-loaded PEGECAT NPs can penetrate the skin not only via appendage routes but also via epidermal routes. This nanotechnology has potential application in transdermal drug delivery. Keywords: poly{[α-maleic anhydride-ω-methoxy-poly(ethylene glycol]-co-(ethyl cyanoacrylate}, nanoparticles, transdermal drug delivery, D,L-tetrahydropalmatine

Blends of Styrene-Butadiene-Styrene Triblock Copolymer with Random Styrene-Maleic Anhydride Copolymers

NARCIS (Netherlands)

Piccini, Maria Teresa; Ruggeri, Giacomo; Passaglia, Elisa; Picchioni, Francesco; Aglietto, Mauro

2002-01-01

Blends of styrene-butadiene-styrene triblock copolymer (SBS) with random styrene-maleic anhydride copolymers (PS-co-MA), having different MA content, were prepared in a Brabender Plastigraph mixer. The presence of polystyrene (PS) blocks in the SBS copolymer and the high styrene content (93 and 86

Tensile and morphology properties of PLA/LNR blends modified with maleic anhydride grafted-polylactic acid and -natural rubber

Science.gov (United States)

Ruf, Mohd Farid Hakim Mohd; Ahmad, Sahrim; Chen, Ruey Shan; Shahdan, Dalila; Zailan, Farrah Diyana

2018-04-01

This research was carried out to investigate the addition of grafted copolymers of maleic anhydride grafted-polylactic acid(PLA-g-MA) and maleic anhydride grafted-natural rubber (NR-g-MA) on the tensile and morphology properties of polylactic acid/ liquid natural rubber (PLA/LNR) blends. Prior to blend preparation, the PLA-g-MA and NR-g-MA was first self-synthesized using maleic anhydride (MA) and dicumyl peroxide (DCP) as initiator together with the PLA and NR respectively. The PLA/LNR, PLA/LNR/PLA-g-MA and PLA/LNR/NR-g-MA blends were prepared via melt-blending method. The loading of PLA-g-MA and NR-g-MA was varied by 5, 10 and 15 wt% respectively. The addition of PLA-g-MA led to increment in tensile strength with 5 and 10 wt% while NR-g-MA gives lower than controlled sample (PLA/LNR blend). Scanning electron microscope (SEM) showed the interaction of the components in the blends. The PLA/LNR compatibilized with PLA-g-MA and NR-g-MA shows greater dispersion and adhesion.

Designing maleic anhydride-{alpha}-olifin copolymeric combs as wax crystal growth nucleators

Energy Technology Data Exchange (ETDEWEB)

Soni, Hemant P. [Department of Chemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara-390 002 (India); Kiranbala; Bharambe, D.P. [Department of Applied Chemistry, Faculty of Technology and Engineering, The Maharaja Sayajirao University of Baroda, Vadodara-390 001 (India); Agrawal, K.S. [Department of Petrochemical Technology, Polytechnic, The Maharaja Sayajirao University of Baroda, Vadodara-390 002 (India); Nagar, A. [MH ASSET, ONGC, Mumbai (India)

2010-09-15

Modification of the wax crystal habit is of great practical interest during transportation and processing of crude oil at low temperature. Various pour point depressant (PPD) additives can facilitate this modification by different mechanisms. Comb shaped polymer additives are known to depress the pour point of crude oil by providing different nucleation sites for the precipitation of wax. This paper describes performance based design, synthesis, characterization and evaluation of comb shaped polymeric diesters. Copolymers of maleic anhydride with different unsaturated C{sub 22} esters were synthesized and copolymers then reacted with two unsaturated fatty alcohols. All products were characterized by Fourier Transform Infra Red (FTIR) spectroscopy and Gel Permeation Chromatography (GPC). Rheological properties of crude (with and without additive) were studied by Advance Rheometer AR-500. In this study the additive based on oleic acid was evaluated as good PPD and rheology modifier. (author)

Development of chitosan derivatives with anhydride maleic; Desenvolvimento de derivados de quitosana com anidrido maleico

Energy Technology Data Exchange (ETDEWEB)

Silva, Solranny C.C.C.; Braz, Elton Marks de A.; Brito, Carla Adriana R. de S.; Silva, Durcilene A. da; Junior, Luiz de S.S.; Silva Filho, Edson C. da, E-mail: solbiologa@hotmail.com [Universidade Federal do Piaui (UFPI), Teresina, PI (Brazil)

2015-07-01

Chitosan was chemically modified with maleic anhydride in ratios of 1/2, 1/5 and 1/10 in the absence of solvents. The obtained derivatives were characterized by elemental analysis, FTIR, thermal analysis (TGA / DTG) and XRD where it was possible to prove the chemical modification. Elemental analysis showed an increase of the relation C / N with the increasing of the proportion of anhydrides. The FTIR showed the incorporation of the anhydride in the biopolymer structure. The thermal stability of the derivatives was lower in comparison to the polysaccharide and by XRD the modified materials were less crystalline. (author)

Samarium-modified vanadium phosphate catalyst for the selective oxidation of n-butane to maleic anhydride

International Nuclear Information System (INIS)

Wu, Hua-Yi; Wang, Hai-Bo; Liu, Xin-Hua; Li, Jian-Hui; Yang, Mei-Hua; Huang, Chuan-Jing; Weng, Wei-Zheng; Wan, Hui-Lin

2015-01-01

Graphical abstract: The addition of a small amount of Sm into VPO catalyst brought about great changes in its physicochemical properties such as surface area, surface morphology, phase composition and redox property, thus leading to a higher catalytic performance in the selective oxidation of n-butane to maleic anhydride, as compared to the undoped VPO catalyst. - Highlights: • The addition of Sm leads to great changes in the structure of VPO catalyst. • Sm improves performance of VPO for oxidation of n-butane to maleic anhydride. • Catalytic performance is closely related to structure of VPO catalyst. - Abstract: A series of samarium-modified vanadium phosphate catalysts were prepared and studied in selective oxidation of n-butane to maleic anhydride. The catalytic evaluation showed that Sm modification significantly increased the overall n-butane conversion and intrinsic activity. N 2 -adsorption, XRD, SEM, Raman, XPS, EPR and H 2 -TPR techniques were used to investigate the intrinsic difference among these catalysts. The results revealed that the addition of Sm to VPO catalyst can increase the surface area of the catalyst, lead to a significant change in catalyst morphology from plate-like structure into rosette-shape clusters, and largely promote the formation of (VO) 2 P 2 O 7 . All of these were related to the different catalytic performance of Sm-doped and undoped VPO catalysts. The roles of the different VOPO 4 phases and the influence of Sm were also described and discussed

Highly Efficient Gas-Phase Oxidation of Renewable Furfural to Maleic Anhydride over Plate Vanadium Phosphorus Oxide Catalyst.

Science.gov (United States)

Li, Xiukai; Ko, Jogie; Zhang, Yugen

2018-02-09

Maleic anhydride (MAnh) and its acids are critical intermediates in chemical industry. The synthesis of maleic anhydride from renewable furfural is one of the most sought after processes in the field of sustainable chemistry. In this study, a plate vanadium phosphorus oxide (VPO) catalyst synthesized by a hydrothermal method with glucose as a green reducing agent catalyzes furfural oxidation to MAnh in the gas phase. The plate catalyst-denoted as VPO HT -has a preferentially exposed (200) crystal plane and exhibited dramatically enhanced activity, selectivity and stability as compared to conventional VPO catalysts and other state-of-the-art catalytic systems. At 360 °C reaction temperature with air as an oxidant, about 90 % yield of MAnh was obtained at 10 vol % of furfural in the feed, a furfural concentration value that is much higher than those (<2 vol %) reported for other catalytic systems. The catalyst showed good long-term stability and there was no decrease in activity or selectivity for MAnh during the time-on-stream of 25 h. The high efficiency and catalyst stability indicate the great potential of this system for the synthesis of maleic anhydride from renewable furfural. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Effect of maleic anhydride on the physico-mechanical properties of NR/PE blends

International Nuclear Information System (INIS)

Yehia, A.A.; El Elnashar, D.

2005-01-01

Blending of two or more polymers is considered as a new technique to produce new materials with new properties at low production cost and investment. Rubber / Rubber blends are well known in tire industry. In the last decade rubber and plastic blending attract the interest of many researchers and technologists. In the present work NR and LLDPE was blended in presence of maleic anhydride (MA) on a Brabender premixed at different conditions and namely temperature and time. The obtained blends were cured with sulphur and peroxide curing systems. Peroxide can crosslink both NR and PE, but the sulphur system crosslinks only the rubber phase in the blend. The data showed also that the addition of MA greatly improved the physico-mechanical properties of NR/PE blends. The surface morphology of the blends under investigation was studied by SEM. The results will be presented and discussed in detail

Separator Membrane from Crosslinked Poly(Vinyl Alcohol and Poly(Methyl Vinyl Ether-alt-Maleic Anhydride

Directory of Open Access Journals (Sweden)

Charu Vashisth Rohatgi

2015-03-01

Full Text Available In this work, we report separator membranes from crosslinking of two polymers, such as poly vinyl alcohol (PVA with an ionic polymer poly(methyl vinyl ether-alt-maleic anhydride (PMVE-MA. Such interpolymer-networked systems were extensively used for biomedical and desalination applications but they were not examined for their potential use as membranes or separators for batteries. Therefore, the chemical interactions between these two polymers and the influence of such crosslinking on physicochemical properties of the membrane are systematically investigated through rheology and by critical gel point study. The hydrogen bonding and the chemical interaction between PMVE-MA and PVA resulted in highly cross-linked membranes. Effect of the molecular weight of PVA on the membrane properties was also examined. The developed membranes were extensively characterized by studying their physicochemical properties (water uptake, swelling ratio, and conductivity, thermal and electrochemical properties using differential scanning calorimetry (DSC, dynamic mechanical analysis (DMA, thermo-gravimetric analysis (TGA and electrochemical impedance spectroscopy (EIS. The DSC study shows the presence of a single Tg in the membranes indicating compatibility of the two polymers in flexible and transparent films. The membranes show good stability and ion conductivity suitable for separator applications.

Separator Membrane from Crosslinked Poly(Vinyl Alcohol) and Poly(Methyl Vinyl Ether-alt-Maleic Anhydride)

Science.gov (United States)

Rohatgi, Charu Vashisth; Dutta, Naba K.; Choudhury, Namita Roy

2015-01-01

In this work, we report separator membranes from crosslinking of two polymers, such as poly vinyl alcohol (PVA) with an ionic polymer poly(methyl vinyl ether-alt-maleic anhydride) (PMVE-MA). Such interpolymer-networked systems were extensively used for biomedical and desalination applications but they were not examined for their potential use as membranes or separators for batteries. Therefore, the chemical interactions between these two polymers and the influence of such crosslinking on physicochemical properties of the membrane are systematically investigated through rheology and by critical gel point study. The hydrogen bonding and the chemical interaction between PMVE-MA and PVA resulted in highly cross-linked membranes. Effect of the molecular weight of PVA on the membrane properties was also examined. The developed membranes were extensively characterized by studying their physicochemical properties (water uptake, swelling ratio, and conductivity), thermal and electrochemical properties using differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), thermo-gravimetric analysis (TGA) and electrochemical impedance spectroscopy (EIS). The DSC study shows the presence of a single Tg in the membranes indicating compatibility of the two polymers in flexible and transparent films. The membranes show good stability and ion conductivity suitable for separator applications. PMID:28347019

Biomimetic porous high-density polyethylene/polyethylene- grafted-maleic anhydride scaffold with improved in vitro cytocompatibility.

Science.gov (United States)

Sharma, Swati; Bhaskar, Nitu; Bose, Surjasarathi; Basu, Bikaramjit

2018-05-01

A major challenge for tissue engineering is to design and to develop a porous biocompatible scaffold, which can mimic the properties of natural tissue. As a first step towards this endeavour, we here demonstrate a distinct methodology in biomimetically synthesized porous high-density polyethylene scaffolds. Co-extrusion approach was adopted, whereby high-density polyethylene was melt mixed with polyethylene oxide to form an immiscible binary blend. Selective dissolution of polyethylene oxide from the biphasic system revealed droplet-matrix-type morphology. An attempt to stabilize such morphology against thermal and shear effects was made by the addition of polyethylene- grafted-maleic anhydride as a compatibilizer. A maximum ultimate tensile strength of 7 MPa and elastic modulus of 370 MPa were displayed by the high-density polyethylene/polyethylene oxide binary blend with 5% maleated polyethylene during uniaxial tensile loading. The cell culture experiments with murine myoblast C2C12 cell line indicated that compared to neat high-density polyethylene and high-density polyethylene/polyethylene oxide, the high-density polyethylene/polyethylene oxide with 5% polyethylene- grafted-maleic anhydride scaffold significantly increased muscle cell attachment and proliferation with distinct elongated threadlike appearance and highly stained nuclei, in vitro. This has been partly attributed to the change in surface wettability property with a reduced contact angle (∼72°) for 5% PE- g-MA blends. These findings suggest that the high-density polyethylene/polyethylene oxide with 5% polyethylene- grafted-maleic anhydride can be treated as a cell growth substrate in bioengineering applications.

Preparation and Characterization of Extruded Composites Based on Polypropylene and Chitosan Compatibilized with Polypropylene-Graft-Maleic Anhydride

Science.gov (United States)

Carrasco-Guigón, Fernando Javier; Rodríguez-Félix, Dora Evelia; Castillo-Ortega, María Mónica; Santacruz-Ortega, Hisila C.; Burruel-Ibarra, Silvia E.; Encinas-Encinas, Jose Carmelo; Plascencia-Jatomea, Maribel; Herrera-Franco, Pedro Jesus; Madera-Santana, Tomas Jesus

2017-01-01

The preparation of composites of synthetic and natural polymers represent an interesting option to combine properties; in this manner, polypropylene and chitosan extruded films using a different proportion of components and polypropylene-graft-maleic anhydride (PPgMA) as compatibilizer were prepared. The effect of the content of the biopolymer in the polypropylene (PP) matrix, the addition of compatibilizer, and the particle size on the properties of the composites was analyzed using characterization by fourier transform-infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), tensile strength, and contact angle, finding that in general, the addition of the compatibilizer and reducing the particle size of the chitosan, favored the physicochemical and morphological properties of the films. PMID:28772464

Effect of maleic anhydride treatment on the mechanical properties of sansevieria fiber/vinyl ester composites

Science.gov (United States)

Pradipta, Rangga; Mardiyati, Steven, Purnomo, Ikhsan

2017-03-01

Sanseviera trifasciata commonly called mother-in-law tongue also known as snake plant is native to Indonesia, India and Africa. Sansevieria is a new fiber in composite research and has showed promising properties as reinforcement material in polymer matrix composites. Chemical treatment on reinforcing fiber is crucial to reduce hydrophilic tendency and thus improve compatibility with the matrix. In this study, effect of maleic anhydride as chemical treatment on the mechanical properties of Sansevieria fiber/vinyl ester composite was investigated. Sansevieria fibers were immersed by using NaOH 3% for two hours at 100°C and then treated by using maleic anhydrate for two hours at 120°C. Composites were prepared by solution casting with various volume fractions of fiber; 0%, 2.5%, 5%, 7.5% and 10%. Actual density, volume fraction of void and mechanical properties of composite were conducted according to ASTM standard testing methods D792, D3171 and D3039. It was found that mechanical properties of composites increased as volume fractions of fiber was increased. The highest tensile strength and modulus of elasticity of composites were 57.45 MPa and 3.47 GPa respectively, obtained from composites with volume fraction of fiber 10%.

Compatibility analysis of Nylon 6 and poly(ethylene-n-butyl acrylate-maleic anhydride) elastomer blends using isothermal crystallization kinetics

Energy Technology Data Exchange (ETDEWEB)

Biber, Erkan, E-mail: ebiber@cankaya.edu.tr [Middle East Technical University, Polymer Science and Technology Department, Ankara (Turkey); Cankaya University, Industrial Engineering Department, Ankara (Turkey); Guenduez, Guengoer [Middle East Technical University, Polymer Science and Technology Department, Ankara (Turkey); Middle East Technical University, Chemical Engineering Department, Ankara (Turkey); Mavis, Bora [Hacettepe University, Mechanical Engineering Department, Ankara (Turkey); Colak, Uner [Hacettepe University, Nuclear Energy Engineering Department, Ankara (Turkey)

2010-07-01

Nylon 6 is a widely used engineering polymer, and has relatively poor impact strength. Ethylene, n-Butyl acrylate, maleic anhydride (E-nBA-MAH) terpolymer is blended with Nylon 6 to enhance its impact strength. Mixture should be compatible to be used in applications. The bare interaction energy between Nylon 6 and E-nBA-MAH terpolymer is calculated according to melting point depression approach using both Flory-Huggins (FH) Theory and Sanchez-Lacombe Equation of State (SL EOS). It demonstrates that blends are thermodynamically favorable to any arrangements. Yet, isothermal crystallization kinetics and WAXS crystallization peaks of blends reveal that mixtures of various compositions have different crystallization behaviors and require alternating crystallization energy due to crystalline structures of individual polymers. Also, SEM images support that after 5% addition of elastomeric terpolymer, interaction loosens due to strong crystalline structure of Nylon 6.

A novel reverse osmosis membrane modified by polyvinyl alcohol with maleic anhydride crosslinking

Science.gov (United States)

Samnani, Mohit; Rathod, Harshad; Raval, Hiren

2018-03-01

In the era of increasing energy crisis, it is inevitable to decrease process energy consumption to increase process viability and curtail green-house gas emission. The Reverse Osmosis plant requires significant energy to transfer water overcoming the osmotic pressure. This paper focuses on increasing the water flux for Thin Film Composite Reverse Osmosis (TFC RO) membrane without compromising salt rejection performance leading to the environmentally friendly and economically attractive process. The virgin TFC RO membrane was exposed to solution of sodium hypochlorite of concentration 2000 mg l-1 for 1 h to activate the surface of the membrane, followed by the treatment with the mixture of polyvinyl alcohol and maleic anhydride with varying concentrations for 1 h and curing in the oven at 80 °C temperature for 10 min. Out of all the treated membranes, the membrane treated with 2000 mg l-1 polyvinyl alcohol and 1000 mg l-1 maleic anhydride demonstrated the highest salt rejection of 96.83 % with 2% increase as compared to the virgin TFC RO membrane. The water flux of the membrane was around 44% higher than the virgin TFC RO membrane. The membrane samples were characterized by atomic force micrographs, ATR-FTIR, Nuclear magnetic resonance and Dynamic mechanical analysis.

Partial oxidation of D-xylose to maleic anhydride and acrylic acid over vanadyl pyrophosphate

International Nuclear Information System (INIS)

Ghaznavi, Touraj; Neagoe, Cristian; Patience, Gregory S.

2014-01-01

Xylose is the second most abundant sugar after glucose. Despite its tremendous potential to serve as a renewable feedstock, few commercial processes exploit this resource. Here, we report a new technology in which a two-fluid nozzle atomizes a xylose-water solution into a capillary fluidized bed operating above 300 °C. Xylose-water droplets form at the tip of the injector, vaporize then react with a heterogeneous mixed oxide catalyst. A syringe pump metered the solution to the reactor charged with 1 g of catalyst. Product yield over vanadyl pyrophosphate was higher compared to molybdenum trioxide-cobalt oxide and iron molybdate; it reached 25% for maleic anhydride, 17% for acrylic acid and 11% for acrolein. Gas residence time was 0.2 s. The catalyst was free of coke even after operating for 4 h – based on a thermogravimetric analysis of catalyst withdrawn from the reactor. Below 300 °C, powder agglomerated at the tip of the injector at 300 °C; it also agglomerated with a xylose mass fraction of 7% in water. - Highlights: • D-xylose reacts to form maleic anhydride and acrylic acid above 250 °C. • Vanadyl pyrophosphate is both active and selective for maleic and acrylic acid. • Acid and acrolein yield approaches 50% for a xylose mass fraction of 3% in water. • Catalyst agglomerates at low temperatures and high xylose aqueous mass fraction. • Atomization quality is a determining factor to minimize agglomeration

Blending of Low-Density Polyethylene and Poly-Lactic Acid with Maleic Anhydride as A Compatibilizer for Better Environmentally Food-Packaging Material

Science.gov (United States)

Setiawan, A. H.; Aulia, F.

2017-05-01

The common conventional food packaging materialsare using a thin layer plastic or film, which is made of a synthetic polymer, such as Low-Density Poly Ethylene (LDPE). However, the use of these polymers hasan adverse impact on the environment, because the synthetic polymersare difficult to degrade naturally. Poly-Lactic Acid (PLA) is a biodegradable polymer that can be substituted to synthetic polymers. Since LDPE and PLA have a difference in polarity, therefore the first step of research is to graft them with maleic anhydride (MAH) for increasing the properties of its miscibility. The interaction between them is confirmed by FTIR; whereas the environment issueis characterized by the water adsorption and biodegradability. The FTIR spectra indicated that there had been an interaction between LDPE and MAH and LDPE/LDPE-g-MAH/PLA blend. Increasing PLA content in the blend affected to the increasing in their water absorption and biodegradable. Poly-blend with 20% PLA content was the optimum composition for environmentally food packaging.

Controlled Release of Damascone from Poly(styrene-co-maleic anhydride-based Bioconjugates in Functional Perfumery

Directory of Open Access Journals (Sweden)

Andreas Herrmann

2013-02-01

Full Text Available Poly(styrene-co-maleic anhydrides were modified with poly(propylene oxide (PO-co-ethylene oxide (EO side chains (Jeffamine® with different EO/PO molar ratios, varying between 0.11 and 3.60. These copolymers were then further functionalized with a β-mercapto ketone of δ-damascone. The obtained poly(maleic acid monoamide-based β-mercapto ketones were then studied as delivery systems for the controlled release of δ-damascone by retro 1,4-addition. The release of δ-damascone, a volatile, bioactive molecule of the family of rose ketones, was studied by dynamic headspace analysis above a cotton surface after deposition of a cationic surfactant containing fabric softening formulation, as a function of the ethylene oxide (EO/propylene oxide (PO molar ratio of the grafted copolymer side chains. The polarity of the EO/PO side chain influenced the release efficiency of the damascone in a typical fabric softening application. PO-rich copolymers and the corresponding poly(styrene-co-maleic anhydride without Jeffamine® side chains were found to be less efficient for the desired fragrance release than the corresponding bioconjugate with a EO/PO ratio of 3.60 in the side chain. This copolymer conjugate seemed to represent a suitable balance between hydrophilicity and hydrophobicity to favor the release of the δ-damascone and to improve the deposition of the conjugate from an aqueous environment onto a cotton surface.

The use of maleic anhydride-modified polypropylene for performance enhancement in continuous glass fiber-reinforced polypropylene composites

NARCIS (Netherlands)

Rijsdijk, H.A.; Contant, M.; Peijs, A.A.J.M.; Miravete, A.

1993-01-01

The influence of maleic anhydride-modified polypropylene (m-PP) on static mech. properties of continuous glass fiber-reinforced polypropylene (PP) composites was studied. M-PP was added to the PP homopolymer to improve the adhesion between the matrix and the glass fiber. Three-point bending tests

A maleic anhydride grafted sugarcane bagasse adsorbent and its performance on the removal of methylene blue from related wastewater

Energy Technology Data Exchange (ETDEWEB)

Ge, Mingliang; Du, Mingyi; Zheng, Luoyun [Key Laboratory of Polymer Processing Engineering of Ministry of Education, National Engineering Research Center of Novel Equipment for Polymer Processing, School of Mechanical & Automotive Engineering, South China University of Technology, Guangzhou 510640 (China); Wang, Bingying; Zhou, Xiangyang [College of Chemistry and Chemical Engineering, Zhongkai University of Agriculture and Engineering, Guangzhou 510225 (China); Jia, Zhixin [College of Material Science and Engineering, South China University of Technology, Guangzhou 510640 (China); Hu, Guoqing [Key Laboratory of Polymer Processing Engineering of Ministry of Education, National Engineering Research Center of Novel Equipment for Polymer Processing, School of Mechanical & Automotive Engineering, South China University of Technology, Guangzhou 510640 (China); Jahangir Alam, S.M., E-mail: mejahangir@scut.edu.cn [Key Laboratory of Polymer Processing Engineering of Ministry of Education, National Engineering Research Center of Novel Equipment for Polymer Processing, School of Mechanical & Automotive Engineering, South China University of Technology, Guangzhou 510640 (China)

2017-05-01

Sugarcane bagasse (SCB) was selected as the supporting material for grafting maleic anhydride (MA) to obtain sugarcane-bagasse-grafting-maleic-anhydride (SCB-g-MA), which was used as an adsorbent for the removal of methylene blue (MB) in the dye-containing wastewater. The granular morphology and functional groups of the material were characterized by the scanning electron microscope (SEM), Fourier transforms infrared spectroscopy (FTIR), and solid-state analysis (13C NMR) methods. The effect(s) of the adsorbent dosage, adsorption time, initial concentration of MB, and the pH of solution on the MB adsorption performance of the material have been also investigated. The results showed that the adsorption capacity and removal rate of MB were found to be 82 mg/g and 98%, respectively. It has also showed that the adsorption behavior on the MB could be well described by the pseudo-second-order model integrated with Langmuir model. - Highlights: • Using solid phase grafting method to graft the maleic anhydride (MA) onto the Sugarcane bagasse (SCB) and get the SCB-g-MA. • SEM, FTIR and 13C NMR analysis were used to characterize the grafting of MA on to the SCB by the solid phase grafting method. • The adsorption capacity and removal rate of MB were to be 82 mg/g and 98% respectively, to show an excellent adsorption effect. • Pseudo-second-order model and Langmuir model are better fitted the adsorption kinetics and isotherms in this research.

Using maleic anhydride functionalized graphene oxide for improving the interfacial properties of carbon fiber/BMI composites

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W. Li

2016-11-01

Full Text Available Maleic anhydride functionalized graphene oxide (MAH-GO was synthesized and then introduced into carbon fiber (CF reinforced bismaleimide (BMI composites, with the aim of improving the interfacial adhesion strength between CF and BMI resin. Various characterization techniques including Fourier transform infrared spectroscopy (FT-IR, X-ray photoelectron spectra (XPS and thermogravimetric analysis (TGA demonstrated that the maleic anhydride has been successfully grafted onto the GO surfaces. The study showed that the interlaminar shear strength (ILSS and flexural properties of CF/BMI composites were all improved by the incorporation of GO and MAH-GO, and the MAH-GO showed the substantially improved effect due to the strong interaction between the MAH-GO and the resin matrix. The maximum increment of the ILSS, flexural strength and flexural modulus of composites were 24.4, 28.7 and 49.7%, respectively. Scanning electron microscope (SEM photographs of the fracture surfaces revealed that the interfacial bonding between CF and resin matrix was significantly strengthened by the addition of MAH-GO. The results suggest that this feasible method may be an ideal substitute for the traditional method in the interfacial modification of composites.

The Formation of Polycomplexes of Poly(Methyl Vinyl Ether-Co-Maleic Anhydride and Bovine Serum Albumin in the Presence of Copper Ions

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Karahan Mesut

2014-09-01

Full Text Available The binary and ternary complex formations of poly(methyl vinyl ether-co-maleic anhydride (PMVEMA with copper ions and with bovine serum albumin (BSA in the presence of copper ions in phosphate buffer solution at pH = 7 were examined by the techniques of UV-visible, fluorescence, dynamic light scattering, atomic force microscopy measurements. In the formation of binary complexes of PMVEMA-Cu(II, the addition of copper ions to the solution of PMVEMA in phosphate buffer solution at pH = 7 forms homogeneous solutions when the molar ratio of Cu(II/MVEMA is 0.5. Then the formations of ternary complexes of PMVEMA-Cu(II-BSA were examined. Study analysis revealed that the toxicities of polymer-metal and polymer-metal-protein mixture solutions depend on the nature and ratio of components in mixtures.

MECHANICAL, ELECTRICAL, AND THERMAL PROPERTIES OF MALEIC ANHYDRIDE MODIFIED RICE HUSK FILLED PVC COMPOSITES

OpenAIRE

Navin Chand; Bhajan Das Jhod

2008-01-01

Unmodified and modified rice husk powder filled PVC composites were prepared having different amounts of rice husk powder. Mechanical, thermal, and electrical properties of these composites were determined. The tensile strength of rice husk powder PVC composites having 0, 10, 20, 30, and 40 weight percent of rice husk powder was found to be 33.9, 19.4, 18.1, 14.6, and 9.5 MPa, respectively. Adding of maleic anhydride- modified rice husk powder improved the tensile strength of rice husk powder...

Method for production of dicarbonic acid anhydrides

International Nuclear Information System (INIS)

Mistr, A.; Necas, J.; Polak, V.

1975-01-01

A method is described of producing dicarboxylic acid anhydrides by the reaction of maleic acid anhydride with olefins. The synthesis is initiated by gamma radiation at a total dose of 10 4 to 10 6 rads in the presence of an organic solvent. The addition reactions of maleic acid anhydride to 1-hexadecene, 1-octene and cyclohexene with yields of 43%, 17% and 11%, respectively, are specified. (L.K.)

Irradiation grafting of natural rubber latex with maleic anhydride and its compatibilization of poly(lactic acid)/natural rubber blends

Science.gov (United States)

Pongsathit, Siriwan; Pattamaprom, Cattaleeya

2018-03-01

Maleic anhydride (MA) is an interesting monomer to be grafted onto natural rubber(NR) due to its potential as a compatibilizer of hydrophobic rubbers and polymers with higher polarity. So far, radiation grafting of MA onto NR in latex state has not been reported. In this study, the grafting of NR with MA in latex state was investigated by exposing the latex to cobalt-60 gamma irradiation at a fixed MA content of 9% and a varied absorbed doses from 2 to 10 kGy. The FTIR spectrometer, 1H NMR spectrometer and gel content analysis have confirmed successful grafting of MA onto NR after irradiation. The grafted NRs were then used to increase the compatibility and the impact property of PLA/NR blends. It was found that the highest impact strength of the blends was achieved when the grafting was carried out at the absorbed dose of 4 kGy.

Viscometric investigation of compatibilization of the poly(vinyl chloride)/poly(ethylene-co-vinyl acetate) blends by terpolymer of maleic anhydride styrene vinyl acetate

Science.gov (United States)

İmren, Dilek; Boztuğ, Ali; Yılmaz, Ersen; Zengin, H. Bayram

2008-11-01

In this study, a blend of poly(vinyl chloride) (PVC)/ethylene-co-vinyl acetate (EVA) was compatibilized by terpolymer of maleic anhydride-styrene-vinyl acetate (MAStVA) used as a compatibilizer. It was prepared the blends of 50/50 PVC/EVA containing 2-10% of the terpolymer. The compatibility experiences of these blends were investigated by using viscometric method in the range of concentrations (0.5-2.0 g dL -1) where tetrahydrofuran (THF) is the solvent. The interaction parameter (Δ b) was used to study the miscibility and compatibility of polymer blend in solution, obtained from the modified Krigbaum and Wall theory. Turbidity and FTIR measurements were also used to investigate the miscibility of this pair of polymers. The values of the relative viscosities of the each polymer solution and their blends were measured by a Cannon-Fenske type viscometer. In consequence of the study, it was observed that a considerable improvement was achieved in the miscibility of PVC/EVA blends by adding among 5 and 10 wt% of compatibilizer.

Maleic anhydride as an additive to γ-butyrolactone solutions for Li-ion batteries

International Nuclear Information System (INIS)

Ufheil, Joachim; Baertsch, Martin C.; Wuersig, Andreas; Novak, Petr

2005-01-01

The effect of maleic anhydride (MA) as a new film-forming additive in γ-butyrolactone (GBL)-based electrolytes for use in Li-ion batteries has been studied to advance the understanding of the solid electrolyte interphase (SEI) formation on graphite electrodes. Cyclic voltammetry measurements showed that even small amounts of MA (up to 4 wt.%) improved the lithium intercalation into graphite. The effect of MA was also verified by electrochemical impedance spectroscopy. In situ subtractively normalized interfacial Fourier transform infrared spectroscopy (SNIFTIRS) and differential electrochemical mass spectrometry (DEMS) allowed identification of gas formation and decomposition products during the SEI formation. GBL-based electrolytes with MA showed both, higher cycling efficiency and cycle life of graphite electrodes

Oil recovery with sulfomethylated poly (lower alkyl vinyl ether/maleic anhydride)

Energy Technology Data Exchange (ETDEWEB)

Norton, C.J.; Falk, D.O.

1973-05-22

Lower alkyl vinyl ether e.g., methyl vinyl ether, propyl vinyl ether, isopropyl vinyl ether, hexyl vinyl ether, is copolymerized conventionally with maleic anhydride, the resulting copolymer is treated with ammonia or ammonium hydroxide to form the partial amide-ammonium salt, and this salt is in turn treated with formaldehyde and thereafter or simultaneously with ammonium or alkali metal salt sulfite (including bisulfites, etc.) to form an at least partially sulfomethylated copolymer. Aqueous solutions of the sulfomethylated copolymer are useful in increasing the viscosity of drive fluids used in the supplemented recovery of petroleum from subterranean formations. In general, enhancing the polyionic character of mobility control agents used in supplemented recovery of petroleum provides enhanced recovery. Achieving this enhancement of polyionic character through use of sulfonate groups provides a mobility control agent with good ability to sustain viscosity in the presence of brine and lime, usually present in the connate waters of petroleum-bearing formations. (7 claims)

Short-chain grafting of tetrahydrofuran and 1,4-dioxane cycles on vinylchloride-maleic anhydride copolymer

Directory of Open Access Journals (Sweden)

2009-01-01

Full Text Available Mass increase of vinylchloride-maleic anhydride (VC-MA copolymer samples aged in tetrahydrofuran (THF or in 1,4-dioxane results from chemical interaction of VC-MA macromolecules with 1,4-dioxane or THF. Microstructure of the products of such modification was proved by infrared spectroscopy (IR- and nuclear magnetic resonance spectroscopy (13C NMR and 1H NMR. Mechanism of modification has been proposed. The results of microstructure research of VC-MA samples aged in THF and in 1,4-dioxane coincide with already known data on the reactions of opening of these and other oxygen-containing cycles under mild conditions.

Controlled radical copolymerization of styrene and maleic anhydride and the synthesis of novel polyolefin-based block copolymers by reversible addition-fragmentation chain-transfer (RAFT) polymerization

NARCIS (Netherlands)

Brouwer, de J.A.M.; Schellekens, M.A.J.; Klumperman, B.; Monteiro, M.J.; German, A.L.

2000-01-01

Reversible addn.-fragmentation chain transfer (RAFT) was applied to the copolymn. of styrene and maleic anhydride. The product had a low polydispersity and a predetd. molar mass. Novel, well-defined polyolefin-based block copolymers were prepd. with a macromol. RAFT agent prepd. from a com.

Preparation of High Density Polyethylene/Waste Polyurethane Blends Compatibilized with Polyethylene-Graft-Maleic Anhydride by Radiation

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Jong-Seok Park

2015-04-01

Full Text Available Polyurethane (PU is a very popular polymer that is used in a variety of applications due to its good mechanical, thermal, and chemical properties. However, PU recycling has received significant attention due to environmental issues. In this study, we developed a recycling method for waste PU that utilizes the radiation grafting technique. Grafting of waste PU was carried out using a radiation technique with polyethylene-graft-maleic anhydride (PE-g-MA. The PE-g-MA-grafted PU/high density polyethylene (HDPE composite was prepared by melt-blending at various concentrations (0–10 phr of PE-g-MA-grafted PU. The composites were characterized using fourier transform infrared spectroscopy (FT-IR, and their surface morphology and thermal/mechanical properties are reported. For 1 phr PU, the PU could be easily introduced to the HDPE during the melt processing in the blender after the radiation-induced grafting of PU with PE-g-MA. PE-g-MA was easily reacted with PU according to the increasing radiation dose and was located at the interface between the PU and the HDPE during the melt processing in the blender, which improved the interfacial interactions and the mechanical properties of the resultant composites. However, the elongation at break for a PU content >2 phr was drastically decreased.

Extraction of Micro- and Nano-Fibrils from Nylon 6/Polypropylene Grafted with Maleic Anhydride/Polypropylene Blended Films

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E. Bagheban Kochak

2013-01-01

Full Text Available Atechnical feasibility study has been conducted on production of nano- and micro-fibrils from nylon 6/polypropylene grafted with maleic anhydride/polypropylene blended films. Fibrils are prepared in four consecutive steps.In the first step the polymers melt blended in an extruder with and without compatibilizers to produce chips; in the second step films are extruded from polymer blends chips, in the third step films are cold drawn with different draw ratios at room temperature and in the forth step fibrils are extracted by Soxhlet extraction with formic acid as solvent for nylon 6.  The films and fibrils were examined by scanning electron microscope and FTIR spectroscopy. It is found that the polypropylene dispersed phase deforms and coalesces into elongated fibrils during drawing  operation. The  fibrils’ diameters in the blends containing compatibilizer are more uniform and are smaller than those from films without compatibilizers. The thinnest polypropylene fibril observed has a diameter around 300 nm with the aspect ratio above 150. The stress-elongation curves show three distinctive regions, elastic, yield and hardening-leading to breakage. The elastic region is short and follows by necking and yield, i.e., elongation without increase in load. The hardening region is accompanied by the increase in the slope. The deformations of the polypropylene particles are noticed during the last regions of the extension; the fibril deformations seem to be more severe during breakage.

Amphiphilic graft copolymer based on poly(styrene-co-maleic anhydride with low molecular weight polyethylenimine for efficient gene delivery

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Duan XP

2012-09-01

Full Text Available Xiaopin Duan,1,2 Jisheng Xiao,2 Qi Yin,2 Zhiwen Zhang,2 Shirui Mao,1 Yaping Li21School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, 2Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, ChinaBackground and methods: A new amphiphilic comb-shaped copolymer (SP was synthesized by conjugating poly(styrene-co-maleic anhydride with low molecular weight polyethyleneimine for gene delivery. Fourier transform infrared spectrum, 1H nuclear magnetic resonance, and gel permeation chromatography were used to characterize the graft copolymer.Results: The buffering capability of SP was similar to that of polyethyleneimine within the endosomal pH range. The copolymer could condense DNA effectively to form complexes with a positive charge (13–30 mV and a small particle size (130–200 nm at N/P ratios between 5 and 20, and protect DNA from degradation by DNase I. In addition, SP showed much lower cytotoxicity than polyethyleneimine 25,000. Importantly, the gene transfection activity and cellular uptake of SP-DNA complexes were all markedly higher than that of complexes of polyethyleneimine 25,000 and DNA in MCF-7 and MCF-7/ADR cell lines.Conclusion: This work highlights the promise of SP as a safe and efficient synthetic vector for DNA delivery.Keywords: poly(styrene-co-maleic anhydride, polyethylenimine, DNA, gene delivery

Improved performance of Nb-doped vanadyl pyrophosphate, catalyst for n-butane oxidation to maleic anhydride

Energy Technology Data Exchange (ETDEWEB)

Pavarelli, G.; Caldarelli, A.; Cavani, F. [Bologna Univ. (Italy). Dipt. di Chimica Industriale ' Toso Montanari' ; Cortelli, C.; Luciani, S. [Polynt SpA, Scanzorosciate (Italy)

2013-11-01

We report here about an investigation on the role of Nb{sup 5+} when used as a promoter for vanadyl pyrophosphate, catalyst for the oxidation of n-butane to maleic anhydride. The effect of Nb was very complex, a function of both its amount and the reaction temperature used. The optimal catalytic behavior was shown for very low Nb contents, i.e., for a V/Nb atomic ratio as low as 150. The main role of Nb was that of accelerating the formation of a limited amount of {gamma}-VOPO{sub 4} on the surface of vanadyl pyrophosphate, by accelerating the oxidation of V{sup 4+} into V{sup 5+} under reaction conditions. (orig.)

Physico-mechanical properties of silanized-montmorillonite reinforced chitosan-co-poly(maleic anhydride) composites

Science.gov (United States)

Saputra, O. A.; Fajrin, A.; Nauqinida, M.; Suryanti, V.; Pramono, E.

2017-07-01

To solve the problems of dependence on petroleum as starting material in the manufacturing of plastics in Indonesia, green plastic from biopolymer like chitosan to be one of promising options and alternative to replace the conventional plastics. However, to overcome the mechanical and physical properties of chitosan, the addition of reinforcement agent was introduced. In this study, silanized-montmorillonite (sMMt) has been prepared as a reinforcement agent in the chitosan-co-poly(maleic anhydride) (referred as Cs-MAH) matrix. Silanizing of montmorillonite is one of strategy to improve the interaction between montmorillonite and chitosan, consequently, the mechanical properties, tensile strength of composites contained 6 phr of sMMt improved 56.5% to chitosan. Moreover, the presence both MAH and sMMt on the comosites also reduced swelling degree and swelling area by 20.6% and 26.7%.

Effect of surface modified kaolin on properties of polypropylene grafted maleic anhydride

Science.gov (United States)

Yang, Ni; Zhang, Zuo-Cai; Ma, Ning; Liu, Huan-Li; Zhan, Xue-Qing; Li, Bing; Gao, Wei; Tsai, Fang-Chang; Jiang, Tao; Chang, Chang-Jung; Chiang, Tai-Chin; Shi, Dean

To achieve reinforcement of mechanical and thermal performances of polypropylene (PP) product, this work aimed at fabrication of surface modified kaolin (M-kaolin) filled polypropylene grafted maleic anhydride (PP-g-MAH) composites with varying contents of fillers and investigation of their mechanical and thermal properties. And the prepared PP-g-MAH/M-kaolin composites were characterized by means of Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). Fracture analysis by SEM showed M-kaolin particles were well dispersed in the PP-g-MAH matrix. Mechanical behaviors were determined by tensile strength, tensile strain at break and impact strength analysis. Impact strength of PP-g-MAH/2 wt% M-kaolin composites was improved up to 30% comparing with unfilled composites. Thermostability had been found enhanced when M-kaolin added. The results revealed PP-g-MAH/M-kaolin composites showed the optimal thermal and mechanical properties when 2 wt% of M-kaolin was added.

nanocomposites of PA6/ABS blends compatibilized with styrene-maleic anhydride copolymer

International Nuclear Information System (INIS)

Oliveira, Amanda D. de; Pessan, Luiz A.

2009-01-01

To achieve a balance between stiffness and toughness, ternary nanocomposites based on blends of polyamide 6 (PA6) and acrylonitrile-butadiene-styrene (ABS) were prepared by the melt intercalation using the organoclay Cloisite R 30B (OMMT) and the styrene-maleic anhydride copolymer (SMA) as compatibilizer. Four blending sequences were used to prepare studied systems and their mechanical properties studied through the Young's modulus and notched Izod impact. It was observed that the materials prepared by all blending sequences studied showed an increase in the Young's modulus compared to the neat PA6. However, a decrease in the toughness was observed for the systems with the addition of the organoclay. The DRX results showed an intercalated structure for the some systems that used ABS in their compositions. HDT measurements of the nanocomposites showed an increase in this property compared to the neat PA6. The use of nanoclay lead to a reinforcement of the polymeric matrix. (author)

Morphology, rheology and electrical resistivity of PLLA/HDPE/CNT nanocomposites: Effect of maleic anhydride

Energy Technology Data Exchange (ETDEWEB)

Shao, Li-na; Chen, Jie; Dai, Jian; Chen, Hai-ming; Yang, Jing-hui [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Wang, Yong, E-mail: yongwang1976@163.com [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Zhang, Chao-liang [State Key Laboratory of Oral Diseases, Sichuan University, Chengdu 610041 (China)

2015-02-15

As a part of serial work about tuning the selective location of carbon nanotubes (CNTs) in immiscible polymer blends, this work reports the effects of component polarity and viscosity ratio between components on the selective location of CNTs and the resultant electrical resistivity of the nanocomposites. To achieve the research aim, maleic anhydride (MA) was grafted onto poly(L-lactide) (PLLA) main chain through a reactive compounding processing. After that, different contents of CNTs were incorporated into blends of high density polyethylene (HDPE) and PLLA (or PLLA-g-MA). The morphologies of the ternary nanocomposites and the selective location of CNTs in the nanocomposites were characterized using scanning electron microscope (SEM) and transmission electron microscope (TEM). The microstructure of nanocomposites and the dispersion of CNTs were further proved by rheological measurement. Finally, the electrical resistivity of nanocomposites containing different CNT contents was measured. The results showed that through increasing the polarity of PLLA and decreasing the melt viscosity, CNTs were kinetically trapped at the blend interface region. Consequently, largely decreased percolation threshold was achieved for the PLLA-g-MA/HDPE/CNT nanocomposites. The morphological changes as well as the rheological properties were also comparatively analyzed. - Highlights: • PLLA/HDPE/CNT and PLLA-g-MA/HDPE/CNT composites were prepared. • Different selective location states of CNTs were achieved in different composites. • Selectively located CNTs at the interface resulted in lower percolation threshold.

Autophobicity and layering behavior of thin liquid-crystalline polymer films.

NARCIS (Netherlands)

Wielen, van der M.W.J.; Cohen Stuart, M.A.; Fleer, G.J.

1998-01-01

The stability against breaking-up of thin spin-coated films of liquid-crystalline polymers depends on the film thickness and annealing temperature. This study concerns side-chain liquid-crystalline polymers, based on alternating copolymers of maleic anhydride and mesogenic alkenes. The mesogenic

PREPARATION AND CHARACTERIZATION OF COMPOSITES COMPRISING MODIFIED HARDWOOD AND WOOD POLYMERS/POLY(VINYL CHLORIDE

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Ruxanda Bodîrlău

Full Text Available Chemical modification of hardwood sawdust from ash-tree species was carried out with a solution of maleic anhydride in acetone. Wood polymers, lignin, and cellulose were isolated from the wood sawdust and modified by the same method. Samples were characterized by Fourier transform infrared spectroscopy (FTIR, providing evidence that maleic anhydride esterifies the free hydroxyl groups of the wood polymer components. Composites comprising chemically modified wood sawdust and wood polymers (cellulose, lignin-as variable weight percentages-, and poly (vinyl chloride were obtained and further characterized by using FTIR spectroscopy and scanning electron microscopy (SEM. The thermal behavior of composites was investigated by using the thermogravimetric analysis (TGA. In all cases, thermal properties were affected by fillers addition.

Study of maleic anhydride and styrene grafted onto polypropylene induced by UV irradiation

International Nuclear Information System (INIS)

Li Zhenzhong; He Wei; Guo Hongjun; Zhang Wenxiong; Ma Yalin

2007-01-01

Maleic anhydride (MAH) and styrene (St) grafted onto polypropylene (PP) were prepared by UV irradiation. Effects of the irradiation time, monomer and initiator content on the grafting rate and melt flow rate (MFR) were studied. The results show that the optimal duration of UV irradiation is 30s. The grafting rate increases with initiator content when initiator content less than 0.6 phr, the MFR value of grafted PP reaches the highest point when benzophenone (BP) content is 0.4 phr. The content of MAH and St have an effect on the grafting rate and MFR value of the grafted PP, and the optimal contents of monomer is 4 phr. The existence of St as a comonomer reduces apparently the MFR value of grafted PP greatly. Grafted PP present significant changes in crystallization and fusion peaks, indicating differences in crystal size and formation after grafting reaction. (authors)

Tailoring magnetic properties of self-biased hexaferrites using an alternative copolymer of isobutylene and maleic anhydride

Science.gov (United States)

Wu, Chuanjian; Yu, Zhong; Sokolov, Alexander S.; Yu, Chengju; Sun, Ke; Jiang, Xiaona; Lan, Zhongwen; Harris, Vincent G.

2018-05-01

Discussed is a novel self-biased hexaferrite gelling system based on a nontoxic and water-soluble copolymer of isobutylene and maleic anhydride. This copolymer simultaneously acts as a dispersant and gelling agent, and recently received much attention from the ceramics community. Herein its effects on the rheological conditions throughout magnetic-field pressing, and consequently, orientation, density and magnetic properties of textured hexaferrites were investigated. Ka-band FMR linewidths were measured, and the crystalline anisotropy and porosity induced linewidth broadening were estimated according to Schlömann's theory. The copolymer allowed to reduce the friction between micron-sized magnetic particulates, resulting in higher density and degree of crystalline orientation, and lower FMR linewidth.

Effect of hydrostatic pressure, temperature, and solvent on the rate of the Diels-Alder reaction between 9,10-anthracenedimethanol and maleic anhydride

Science.gov (United States)

Kiselev, V. D.; Kornilov, D. A.; Anikin, O. V.; Latypova, L. I.; Konovalov, A. I.

2017-03-01

The rate of the reaction between 9,10-anthracenedimethanol and maleic anhydride in 1,4-dioxane, acetonitrile, trichloromethane, and toluene is studied at 25, 35, 45°C in the pressure range of 1-1772 bar. The rate constants, enthalpies, entropies and activation volumes are determined. It is shown that the rate of reaction with 9,10-anthracenedimethanol is approximately one order of magnitude higher than with 9-anthracenemethanol.

78 FR 76567 - Tall Oil, Polymer With Polyethylene Glycol and Succinic Anhydride Monopolyisobutylene Derivs...

Science.gov (United States)

2013-12-18

..., Polymer With Polyethylene Glycol and Succinic Anhydride Monopolyisobutylene Derivs.; Tolerance Exemption... an exemption from the requirement of a tolerance for residues of tall oil, polymer with polyethylene..., polymer with polyethylene glycol and succinic anhydride monopolyisobutylene derivs. on food or feed...

Partial oxidation of Raffinate II and other mixtures of n-Butane and n-Butenes to maleic anhydride in a fixed-bed reactor

OpenAIRE

Brandstädter, Willi Michael

2008-01-01

The utilisation of the C4 streams of steamcrackers by converting raffinate II to maleic anhydride was studied. The oxidation reactions were investigated in a laboratory-scale fixed-bed reactor to determine reaction kinetics. The effects of pore diffusional resistance were investigated and explained. A two-dimensional pseudo-homogeneous reactor model was used for the simulation of a production-scale fixed-bed reactor. A flow scheme of the reactor section including a recycle was proposed.

Removal of Copper ions from aqueous solutions using polymer derivations of poly (styrene-alt-maleic anhydride

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Naser Samadi

2017-06-01

Full Text Available In this study chelating resins have been considered to be suitable materials for the recovery of Copper (II ions in water treatments. Furthermore, these modified resins were reacted with 1,2-diaminoethane in the presence of ultrasonic irradiation for the preparation of a tridimensional chelating resin on the Nano scale for the recovery of Copper (II ions from aqueous solutions. This method which is used for removing and determining Copper (II ions using copolymers derived resins of poly (styrene-alternative-maleic anhydride (SMA and atomic absorption spectroscopy. The method is simple, sensitive, inexpensive and fast. The various parameters such as pH, contact time, concentrations of metal ions, mass of resin, and agitation speed were investigated on adsorption effect. The adsorption behavior of Copper (II ions were investigated by the synthesis of chelating resins at various pHs. The prepared resins showed a good tendency for removing the selected metal ions from aqueous solution, even at an acidic pH. Also, the prepared resins were examined for the removal of Copper (II ions from real samples such as industrial wastewater and were shown to be very efficient at adsorption in the cases of Copper (II ions. The pseudo-first-order, pseudo-second-order, and intra-particle diffusion kinetics equations were used for modeling of adsorption data and it was shown that pseudo-second-order kinetic equation could best describe the adsorption kinetics. The intra-particle diffusion study revealed that external diffusion might be involved in this case. The resins were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction analysis.

Alternating copolymerization of propylene oxide with biorenewable terpene-based cyclic anhydrides: a sustainable route to aliphatic polyesters with high glass transition temperatures.

Science.gov (United States)

Van Zee, Nathan J; Coates, Geoffrey W

2015-02-23

The alternating copolymerization of propylene oxide with terpene-based cyclic anhydrides catalyzed by chromium, cobalt, and aluminum salen complexes is reported. The use of the Diels-Alder adduct of α-terpinene and maleic anhydride as the cyclic anhydride comonomer results in amorphous polyesters that exhibit glass transition temperatures (Tg ) of up to 109 °C. The polymerization conditions and choice of catalyst have a dramatic impact on the molecular weight distribution, the relative stereochemistry of the diester units along the polymer chain, and ultimately the Tg of the resulting polymer. The aluminum salen complex exhibits exceptional selectivity for copolymerization without transesterification or epimerization side reactions. The resulting polyesters are highly alternating and have high molecular weights and narrow polydispersities. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

A computational study of the Diels-Alder reactions between 2,3-dibromo-1,3-butadiene and maleic anhydride

Science.gov (United States)

Rivero, Uxía; Meuwly, Markus; Willitsch, Stefan

2017-09-01

The neutral and cationic Diels-Alder-type reactions between 2,3-dibromo-1,3-butadiene and maleic anhydride have been computationally explored as the first step of a combined experimental and theoretical study. Density functional theory calculations show that the neutral reaction is concerted while the cationic reaction can be either concerted or stepwise. Further isomerizations of the Diels-Alder products have been studied in order to predict possible fragmentation pathways in gas-phase experiments. Rice-Ramsperger-Kassel-Marcus (RRKM) calculations suggest that under single-collision experimental conditions the neutral product may reform the reactants and the cationic product will most likely eliminate CO2.

Effect of Surface Modification of Palygorskite on the Properties of Polypropylene/Polypropylene-g-Maleic Anhydride/Palygorskite Nanocomposites

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David Cisneros-Rosado

2017-01-01

Full Text Available The effect of surface modification of palygorskite (Pal on filler dispersion and on the mechanical and thermal properties of polypropylene (PP/polypropylene grafted maleic anhydride (PP-g-MAH/palygorskite (Pal nanocomposites was evaluated. A natural Pal mineral was purified and individually surface modified with hexadecyl tributyl phosphonium bromide and (3-Aminopropyltrimethoxysilane; the pristine and modified Pals were melt-compounded with PP to produce nanocomposites using PP-g-MAH as compatibilizer. The grafting of Pal surface was verified by FT-IR and the change in surface hydrophilicity was estimated by the contact angle of sessile drops of ethylene glycol on Pal tablets. The extent of Pal dispersion and the degree of improvement in both the mechanical and thermal properties were related to the surface treatment of Pal. Modified Pals were better dispersed during melt processing and improved Young’s modulus and strength; however, maximum deformation tended to decrease. The thermal stability of PP/PP-g-MAH/Pal nanocomposites was considerably improved with the content of modified Pals. The degree of crystallinity increased with Pal content, regardless of the surface modification. Surfactant modified Pal exhibited better results in comparison with silane Pal; it is possible that longer alkyl chains from surfactant molecules promoted interactions with polymer chains, thereby improving nanofiller dispersion and enhancing the properties.

Effect of temperature and ph on the drug release rate from a polymer conjugate system

International Nuclear Information System (INIS)

Kenawy, E.; Abdel-Hay, F.I.; El-Newehy, M.H.; Ottenbrite, R.M.

2005-01-01

Hydroximide and A-methylhydroxamic acid of poly(ethylene-altmaleic anhydride) (average MW 100-500 k) were used as a carrier for a new drug delivery system. The synthesis of the hydroximide and N methylhydroxamic acid of poly(ethylene-alt-maleic anhydride) were carried out by chemical modification of poly(ethylene-alt-maleic anhydride) with hydroxylamine and N-methyl hydroxylamine, respectively, in N,N- dimethylformamide at room temperature to yield water soluble copolymer. Ketoprofen was reacted with hydroximide and N-methylhydroxamic acid derivatives of poly(ethylene-alt-maleic anhydride) using dicyclohexylcarbodiimide as condensation agent at -5 degree C to yield water insoluble ketoprofen conjugates. All products were characterized by elemental analysis, FTIR and 1HNMR spectra. The in-vitro ketoprofen release was carried out by UV spectrophotometer at max =260 nm. The results demonstrated the effectiveness of hydroximide and N-methylhydroxamic acid of polyethylene-alt-maleic anhydride) as a drug delivery system. The release rates were studied at various ph and temperatures. The copolymer-drug adducts released the drug very slowly at the low ph found in the stomach thus protecting the drug from the action of high concentrations of digestive acids. These results showed the usefulness of hydroxamic acid polymer-drug conjugates as a new drug delivery system for drugs to be targeted to sites in the GI system

Antimocrobial Polymer

Science.gov (United States)

McDonald, William F.; Huang, Zhi-Heng; Wright, Stacy C.

2005-09-06

A polymeric composition having antimicrobial properties and a process for rendering the surface of a substrate antimicrobial are disclosed. The composition comprises a crosslinked chemical combination of (i) a polymer having amino group-containing side chains along a backbone forming the polymer, (ii) an antimicrobial agent selected from quaternary ammonium compounds, gentian violet compounds, substituted or unsubstituted phenols, biguanide compounds, iodine compounds, and mixtures thereof, and (iii) a crosslinking agent containing functional groups capable of reacting with the amino groups. In one embodiment, the polymer is a polyamide formed from a maleic anhydride or maleic acid ester monomer and alkylamines thereby producing a polyamide having amino substituted alkyl chains on one side of the polyamide backbone; the crosslinking agent is a phosphine having the general formula (A)3P wherein A is hydroxyalkyl; and the antimicrobial agent is chlorhexidine, dimethylchlorophenol, cetyl pyridinium chloride, gentian violet, triclosan, thymol, iodine, and mixtures thereof.

Analysis physical properties of composites polymer from cocofiber and polypropylene plastic waste with maleic anhydrate as crosslinking agent

Science.gov (United States)

Pelita, E.; Hidayani, T. R.; Akbar, A.

2017-07-01

This research was conducted with the aim to produce composites polymer with polypropylene plastic waste materials and cocofiber which aims to produce wood replacement material in the home furnishings industry. This research was conducted with several stages. The first stage is the process of soaking coco fiber with detergent to remove oil and 2% NaOH. The second stage is to combine the polypropylene plastic waste with cocofiber is a chemical bond, modification by adding maleic anhydride as a crosslinking agent and benzoyl peroxide as an initiator each as much as 1%. Mixing materials done by reflux method using xylene solvent. In this study, carried out a wide range of weight variation of coco fiber are added to the 10, 20, 30, 40 and 50%. The third stage is a polymer composite molding process using hot press at a temperature of 158°C. The results of polymer composites Showed optimum condition on the addition of 40% cocofiber with supple tensile strength value of 90.800 kgf /cm2 and value of elongation break at 3.6726 x 104 (kgf/cm2), melting point at 160.02°C, burning point 463.43°C, residue of TGA is 19%, the density of 0.84 g/mL. From these data, conclude that the resulting polymer composites meet the SNI 03-2105-2006 about ordinary composite polymer and polymer composite structural type 8 regular types from 17.5 to 10.5.

Actinic-radiation curable polymers prepared from a reactive polymer, halogenated cyclic anhydride and glycidyl ester

International Nuclear Information System (INIS)

Pastor, S.D.

1979-01-01

A novel class of photosensitive polymers are disclosed which are prepared by the reaction, preferably in the presence of a catalyst, of a reactive polymer, a halogenated cyclic anhydride and glycidyl ester of an alpha, beta-unsaturated carboxylic acid. These polymers are capable of undergoing vinyl-type polymerization when exposed to actinic radiation

Grafting of copolymer styrene maleic anhydride on poly(ethylene terephthalate) film by chemical reaction and by plasma method

Energy Technology Data Exchange (ETDEWEB)

Bigan, Muriel; Bigot, Julien [Laboratoire de Chimie Organique et Macromoleculaire (UMR 8009), Universite des Sciences et Technologies de Lille, 59655 Villeneuve d' Ascq Cedex (France); Mutel, Brigitte [Laboratoire de Genie des Procedes d' Interactions Fluides reactifs-Materiaux (UPRES-EA 3751), Batiment C5, Universite des Sciences et Technologies de Lille, 59655 Villeneuve d' Ascq Cedex (France)], E-mail: Brigitte.mutel@univ-lille1.fr; Coqueret, Xavier [Laboratoire Reactions Selectives et Applications (UMR-CNRS 6519) Universite de Reims Champagne-Ardennes, B.P. 1039, 51687 Reims Cedex 2 (France)

2008-02-15

This work deals with the chemical grafting of a styrene maleic anhydride copolymer on the surface of a previously hydrolyzed polyethylene terephthalate (PET) film 12 {mu}m thick via covalent bond. Two different ways are studied. The first one involves an activation of the hydrolyzed PET by the triethylamine before the grafting step. In the second one, the copolymer reacts with the 4-dimethylaminopyridine in order to form maleinyl pyridinium salt which reacts with alcohol function of the hydrolyzed PET. Characterization and quantification of the grafting are performed by Fourier transform infrared spectroscopy. Factorial experiment designs are used to optimize the process and to estimate experimental parameters effects. The opportunity to associate the chemical process to a cold remote nitrogen plasma one is also examined.

Fire and heat resistant laminating resins based on maleimido substituted aromatic cyclotriphosphazene polymer

Science.gov (United States)

Kumar, Devendra (Inventor); Fohlen, George M. (Inventor); Parker, John A. (Inventor)

1987-01-01

4-Aminophenoxy cyclotriphosphazenes are reacted with maleic anhydride to produce maleamic acids which are converted to the maleimides. The maleimides are polymerized. By selection of starting materials (e.g., hexakis amino or trisaminophenoxy trisphenoxy cyclotriphosphazenes), selection of molar proportions of reactants, use of mixtures of anhydrides and use of dianhydrides as bridging groups a variety of maleimides and polymers are produced. The polymers have high limiting oxygen indices, high char yields and other useful heat and fire resistant properties making them useful as, for example, impregnants of fabrics.

Effect of polypropylene maleic anhydride (PPMAH) on mechanical and morphological properties of polypropylene (PP)/recycled acrylonitrile butadiene rubber (NBRr)/empty fruit bunch (EFB) composites

Science.gov (United States)

Othman, Nurul Syazwani; Santiagoo, Ragunathan; Abdillahi, Khalid Mohamed; Ismail, Hanafi

2017-07-01

The fabrication of polypropylene (PP)/ recycled acrylonitrile butadiene rubber (NBRr)/ empty fruit bunch (EFB) composites were investigated. The effects of polypropylene maleic anhydride (PPMAH) as a compatibilizer on the mechanical and morphological properties of PP/NBRr/EFB composites were studied. Composites were prepared through melt mixing using heated two roll mill at 180 °C for 9 minutes and rotor speed of 15 rpm. NBRr loading were varied from 0 to 60 phr and PPMAH was fixed for 5 phr. The composites were moulded into a 1 mm thin sheet using hot press machine and then cut into dumbbell shape. The mechanical and morphological properties of composites were examined using universal tensile machine (UTM) and scanning electron microscope (SEM), respectively. Tensile strength and Young's modulus of PP/NBRr/EFB composites decreased with increasing NBRr loading, whilst increasing the elongation at break. However, PPMAH compatibilized composites have resulted 27% to 40% and 25% to 42% higher tensile strength and Young's modulus, respectively, higher compared to uncompatibilized composites. This was due to the better adhesion between PP/NBRr matrices and EFB filler with the presence of maleic anhydride moieties. From the morphological study, the micrograph of PPMAH compatibilized composites has proved the well bonded and good attachments of EFB filler with PP/NBRr matrices which results better tensile strength to the PP/NBRr/EFB composites.

Grafting of Maleic Anhydride onto Polyethylene by Blend Process forEnvironmentally Friendly Plastics

International Nuclear Information System (INIS)

Hendrana, Sunit; Retno-Yusiasih; Sudirman; Ipit-Karyaningsih; Djimat-Lisnawati

2000-01-01

Grafting maleic anhydride (MAH) onto polyethylene is one of the route tomake plastics which can be consumed by microbe in the soil. High temperaturesolution process is one of the method to perform grafting. This method is notreally handy since it involves many steps. Therefore, in this work a simplemethod is performed to graft MAH onto polyethylene, i.e., blending process.As the process occurs in melt, the reaction is more likely to be diffusioncontrol rather than chemical control. Therefore, there are many parameterscan affect the grafting such as temperature of the blending, speed of therotation, concentration of MAH and concentration of dicumyl peroxide (DCP).Preliminary work in our laboratorium found an optimum condition for the firsttwo parameters. Thus, in this work the effect of concentration of MAH and DCPis studied into the effectiveness of grafting process. One of the indicationof unexpected reaction is formation of gel, or in other words the formationof X-link among polyethylene molecules. The grafted polyethylene ischaracterized by calculation of gel content, thermal properties by TG/DTA andFourier Transform Infrared (FTIR). The results show the concentration of MAHand DCP play roles. However, initiator DCP has more significance effect thanthe MAH. (author)

The Free-Radical Copolymerization of Difurylmethane with Maleic

African Journals Online (AJOL)

Prof. Jo Michael

Reaction feeds containing 85 mol % and higher of difurylmethane ... Keywords: difurylmethane; maleic anhydride; copolymerization; thermodecomposition ... delivery apparatus set at 500 psi for a flow rate of 1 cm3 min-1; a Waters model U6K.

Influence of Maleic Anhydride/Glycidyl Methacrylate Cografted Polylactic Acid on Properties of Wood Flour/PLA Composites

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DU Jun

2017-12-01

Full Text Available Graft copolymers of PLA-g-MAH, PLA-g-GMA and PLA-co-MAH/GMA were prepared by means of melt grafting. The structure of the graft copolymers were characterized by FTIR.Wood flour/PLA composites were prepared by injection molding with three kinds of graft copolymers as compatibilizers, and the fractured morphology of composites was investigated by scanning electron microscope (SEM. Results show that there is no obvious phase interface between wood flour and PLA,which indicating the interfacial compatibility of wood flour/PLA composites is improved after adding different graft copolymers. The determination results of mechanical properties, processing flowability and dynamic rheological property of composites prepared with different graft copolymers reveal that, compared to the composite without compatibilizer, the tensile strength and impact strength of wood flour/PLA composites are increased by 9.54% and 7.23% respectively, and the equilibrium torque, shear heat, storage modulus and complex viscosity are all increased after adding maleic anhydride/glycidyl methacrylate cografted polylactic acid.

Anhydric maleic functionalization and polyethylene glycol grafting of lactide-co-trimethylene carbonate copolymers

Energy Technology Data Exchange (ETDEWEB)

Díaz, A.; Valle, L.; Franco, L. del [Departament d' Enginyeria Química, Universitat Politècnica de Catalunya, Av. Diagonal 647, Barcelona E-08028 (Spain); Sarasua, J.R. [Department of Mining-Metallurgy Engineering and Materials Science, University of the Basque Country (UPV/EHU), Bilbao (Spain); Estrany, F. [Departament d' Enginyeria Química, Universitat Politècnica de Catalunya, Av. Diagonal 647, Barcelona E-08028 (Spain); Puiggalí, J., E-mail: Jordi.Puiggali@upc.es [Department of Mining-Metallurgy Engineering and Materials Science, University of the Basque Country (UPV/EHU), Bilbao (Spain)

2014-09-01

Lactide and trimethylene carbonate copolymers were successfully grafted with polyethylene glycol via previous functionalization with maleic anhydride and using N,N′-diisopropylcarbodiimide as condensing agent. Maleinization led to moderate polymer degradation. Specifically, the weight average molecular weight decreased from 36,200 to 30,200 g/mol for the copolymer having 20 mol% of trimethylene carbonate units. Copolymers were characterized by differential scanning calorimetry, thermogravimetry and X-ray diffraction. Morphology of spherulites and lamellar crystals was evaluated with optical and atomic force microscopies, respectively. The studied copolymers were able to crystallize despite the randomness caused by the trimethylene carbonate units and the lateral groups. Contact angle measurements indicated that PEG grafted copolymers were more hydrophilic than parent copolymers. This feature justified that enzymatic degradation in lipase medium and proliferation of both epithelial-like and fibroblast-like cells were enhanced. Grafted copolymers were appropriate to prepare regular drug loaded microspheres by the oil-in-water emulsion method. Triclosan release from loaded microspheres was evaluated in two media. - Highlights: • Pegylated copolymers of lactide and trimethylene carbonate have been synthesized. • Grafting with polyethylene glycol was able via maleic anhydride functionalization. • Drug-loaded microspheres could be prepared from new pegylated copolymers. • Hydrophilicity of lactide/trimethylene carbonate copolymers increased by pegylation. • New pegylated copolymers supported cell adhesion and proliferation.

Carboxy terminated rubber based on natural rubber grafted with acid anhydrides and its adhesion properties

International Nuclear Information System (INIS)

Klinpituksa, P; Kongkalai, P; Kaesaman, A

2014-01-01

The chemical modification of natural rubber by grafting of various polar functional molecules is an essential method, improving the versatility of rubber in applications. This research investigated the preparation of natural rubber-graft-citraconic anhydride (NR-g-CCA), natural rubber-graft-itaconic anhydride (NR-g-ICA), and natural rubber-graft-maleic anhydride (NR-g-MA), with the anhydrides grafted to natural rubber in toluene using benzoyl peroxide as an initiator. Variations of monomer content, initiator content, temperature and reaction time of the grafting copolymerization were investigated. The maximum degrees of grafting were 1.06% for NR-g-CCA, 4.66% for NR-g-ICA, and 5.03% for NR-g-MA, reached using 10 phr citraconic anhydride, 10 phr of itaconic anhydride, or 8 phr of maleic anhydride, 3 phr benzoyl peroxide, at 85, 80 and 80°C for 2, 2 and 3 hrs, respectively. Solvent-based wood adhesives were formulated from these copolymers with various contents of wood resin in the range 10-40 phr. The maximal 289 N/in cleavage peel and 245.7 KPa shear strength for NR-g-MA (5.03% grafting) were obtained at 40 phr wood resin

Resonance energy transfer from quinolinone modified polystyrene-block-poly(styrene-alt-maleic anhydride) copolymer to terbium(III) metal ions

Energy Technology Data Exchange (ETDEWEB)

Výprachtický, Drahomír, E-mail: vyprachticky@imc.cas.cz [Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Heyrovský Sq. 2, 162 06 Prague 6 (Czech Republic); Mikeš, František [New York University Polytechnic School of Engineering, Polymer Research Institute, 6 MetroTech Center, Brooklyn, NY 11201 (United States); Lokaj, Jan; Pokorná, Veronika; Cimrová, Věra [Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Heyrovský Sq. 2, 162 06 Prague 6 (Czech Republic)

2015-04-15

Polystyrene-block-poly(styrene-alt-maleic anhydride) was synthesized by nitroxide mediated radical polymerization and modified with 7-amino-4-methylquinolin-2(1H)-one (I) and methanol. The formed block polymer ligand contained a quinolinone fluorophore (Ω) and carboxyl (III) or sodium carboxylate (IV) binding sites. The ligand-to-metal resonance energy transfer (RET) and ligand binding properties of [III–Tb{sup 3+}] and [IV–Tb{sup 3+}] complexes were investigated by steady-state and time-resolved luminescence spectroscopy in tetrahydrofuran/methanol and/or tetrahydrofuran/deuterated methanol mixtures and compared with those of a low-molecular-weight model ligand, i.e. the sodium salt of N-(4-methyl-2-oxo-1,2-dihydroquinolin-7-yl)succinamic acid (II). The long-lived emission intensities of Tb{sup 3+} at 490, 545, 585, and 620 nm corresponding to the {sup 5}D{sub 4}→{sup 7}F{sub 6}, {sup 5}D{sub 4}→{sup 7}F{sub 5}, {sup 5}D{sub 4}→{sup 7}F{sub 4}, and {sup 5}D{sub 4}→{sup 7}F{sub 3} transitions, respectively, were strongly increased by the addition of ligands in the order [II-Tb{sup 3+}]⪡[III-Tb{sup 3+}]<[IV-Tb{sup 3+}]. The efficiency of energy transfer (E) was evaluated from the emission intensity of the donor (Ω) in the presence or absence of the acceptor (Tb{sup 3+}) depending on the acceptor concentration and ligand neutralization. It was concluded that the macromolecular ligand structural properties (polymer coil and supramolecular structures, e.g. micelles) were responsible for the increase in RET. The time-resolved luminescence measurements revealed that the binding affinity of the ligands II, III, and IV increased in the order IIpolymer (donor) for Tb{sup 3+} (acceptor) luminescence was developed. • Efficient donor–acceptor resonance energy transfer (RET) was found out. • Macromolecular (polymer coil) structure caused a powerful RET and also a supramacromolecular (micelles) structure

Kaolinite Nanocomposite Platelets Synthesized by Intercalation and Imidization of Poly(styrene-co-maleic anhydride

Directory of Open Access Journals (Sweden)

Pieter Samyn

2015-07-01

Full Text Available A synthesis route is presented for the subsequent intercalation, exfoliation and surface modification of kaolinite (Kln by an imidization reaction of high-molecular weight poly(styrene-co-maleic anhydride or SMA in the presence of ammonium hydroxide. In a first step, the intercalation of ammonolyzed SMA by guest displacement of intercalated dimethylsulfoxide has been proven. In a second step, the imidization of ammonolyzed SMA at 160 °C results in exfoliation of the kaolinite layers and deposition of poly(styrene-co-maleimide or SMI nanoparticles onto the kaolinite surfaces. Compared with a physical mixture of Kln/SMI, the chemically reacted Kln/SMI provides more efficient exfoliation and hydrogen bonding between the nanoparticles and the kaolinite. The kaolinite nanocomposite particles are synthesized in aqueous dispersion with solid content of 65 wt %. The intercalation and exfoliation are optimized for a concentration ratio of Kln/SMI = 70:30, resulting in maximum intercalation and interlayer distance in combination with highest imide content. After thermal curing at 135 °C, the imidization proceeds towards a maximum conversion of the intermediate amic acid moieties. The changes in O–H stretching and kaolinite lattice vibrations have been illustrated by infrared and FT-Raman spectroscopy, which allow for a good quantification of concentration and imidization effects.

Design of amine modified polymer dispersants for liquid-phase exfoliation of transition metal dichalcogenide nanosheets and their photodetective nanocomposites

Science.gov (United States)

Lee, Jinseong; Hahnkee Kim, Richard; Yu, Seunggun; Babu Velusamy, Dhinesh; Lee, Hyeokjung; Park, Chanho; Cho, Suk Man; Jeong, Beomjin; Sol Kang, Han; Park, Cheolmin

2017-12-01

Liquid-phase exfoliation (LPE) of transition metal dichalcogenide (TMD) nanosheets is a facile, cost-effective approach to large-area photoelectric devices including photodetectors and non-volatile memories. Non-destructive exfoliation of nanosheets using macromolecular dispersing agents is beneficial in rendering the TMD nanocomposite films suitable for mechanically flexible devices. Here, an efficient LPE of molybdenum disulfide (MoS2) with an amine modified poly(styrene-co-maleic anhydride) co-polymer (AM-PSMA) is demonstrated, wherein the maleic anhydrides were converted into maleic imides with primary amines using N-Boc-(CH2) n -NH2. The exfoliation of nanosheets was facilitated through Lewis acid-base interaction between the primary amine and transition metal. The results demonstrate that the exfoliation depends upon both the fraction of primary amines in the polymer chain and their distance from the polymer backbone. Under optimized conditions of primary amine content and its distance from the backbone, AM-PSMA gave rise to a highly concentrated MoS2 nanosheet suspension that was stable for over 10 d. Exfoliation of several other TMDs was also achieved using the optimized AM-PSMA, indicating the scope of AM-PSMA applications. Furthermore, a flexible composite film of AM-PSMA and MoS2 nanosheets fabricated by vacuum-assisted filtration showed excellent photoconductive performances including a high I on/I off ratio of 102 and a fast photocurrent switching of 300 ms.

The polymerization of furfuryl alcohol with p-toluenesulfonic acid: photo cross-linkable feature of the polymer

International Nuclear Information System (INIS)

Principe, Martha; Martinez, Ricardo; Ortiz, Pedro; Rieumont, Jacques

2000-01-01

Poly (furfuryl alcohol) with different amounts of oxymethylenic bridges was synthesized using trifluoroacetic and p-toluenesulfonic acid. All polymers displayed a tendency to retain acids. The isolated products containing traces of acid became insoluble in a few hours; while neutral material maintains theirs solubility for at least one month. Polymers stored in solution were stable according to their HNMR spectra. Polymers cross-linked after being exposed to UV radiation. The product of the reaction of polymer with maleic anhydride is useful for preparing negative photo resists. (author)

Preparation of a Sepia Melanin and Poly(ethylene-alt-maleic Anhydride Hybrid Material as an Adsorbent for Water Purification

Directory of Open Access Journals (Sweden)

Guido Panzarasa

2018-01-01

Full Text Available Meeting the increasing demand of clean water requires the development of novel efficient adsorbent materials for the removal of organic pollutants. In this context the use of natural, renewable sources is of special relevance and sepia melanin, thanks to its ability to bind a variety of organic and inorganic species, has already attracted interest for water purification. Here we describe the synthesis of a material obtained by the combination of sepia melanin and poly(ethylene-alt-maleic anhydride (P(E-alt-MA. Compared to sepia melanin, the resulting hybrid displays a high and fast adsorption efficiency towards methylene blue (a common industrial dye for a wide pH range (from pH 2 to 12 and under high ionic strength conditions. It is easily recovered after use and can be reused up to three times. Given the wide availability of sepia melanin and P(E-alt-MA, the synthesis of our hybrid is simple and affordable, making it suitable for industrial water purification purposes.

Effects of Polyethylene Grafted Maleic Anhydride on the Mechanical, Morphological, and Swelling Properties of Poly (Vinyl Chloride / Epoxidized Natural Rubber / Kenaf Core Powder Composites

Directory of Open Access Journals (Sweden)

Rohani Abdul Majid

2014-10-01

Full Text Available The effects of polyethylene grafted maleic anhydride (PE-g-MA on the properties of poly (vinyl chloride/epoxidized natural rubber (PVC/ENR kenaf core powder composites were studied, with four different loadings of kenaf core powder (5, 10, 15, and 20 phr. The tensile properties indicated that the strength and elongation at break of the composites exhibited an increase for samples with PE-g-MA. Morphological analysis using a scanning electron microscope (SEM showed better dispersion of kenaf fiber with the addition of PE-g-MA and less kenaf powder agglomeration. Furthermore, the swelling index indicated that composites with PE-g-MA showed lower toluene absorption than composites without PE-g-MA.

Design of a multi-dopamine-modified polymer ligand optimally suited for interfacing magnetic nanoparticles with biological systems.

Science.gov (United States)

Wang, Wentao; Ji, Xin; Na, Hyon Bin; Safi, Malak; Smith, Alexandra; Palui, Goutam; Perez, J Manuel; Mattoussi, Hedi

2014-06-03

We have designed a set of multifunctional and multicoordinating polymer ligands that are optimally suited for surface functionalizing iron oxide and potentially other magnetic nanoparticles (NPs) and promoting their integration into biological systems. The amphiphilic polymers are prepared by coupling (via nucleophilic addition) several amine-terminated dopamine anchoring groups, poly(ethylene glycol) moieties, and reactive groups onto a poly(isobutylene-alt-maleic anhydride) (PIMA) chain. This design greatly benefits from the highly efficient and reagent-free one-step reaction of maleic anhydride groups with amine-containing molecules. The availability of several dopamine groups in the same ligand greatly enhances the ligand affinity, via multiple coordination, to the magnetic NPs, while the hydrophilic and reactive groups promote colloidal stability in buffer media and allow subsequent conjugation with target biomolecules. Iron oxide nanoparticles ligand exchanged with these polymer ligands have a compact hydrodynamic size and exhibit enhanced long-term colloidal stability over the pH range of 4-12 and in the presence of excess electrolytes. Nanoparticles ligated with terminally reactive polymers have been easily coupled to target dyes and tested in live cell imaging with no measurable cytotoxicity. Finally, the resulting hydrophilic nanoparticles exhibit large and size-dependent r2 relaxivity values.

Optimal oxygen feeding policy to maximize the production of Maleic anhydride in unsteady state fixed bed catalytic reactors

Directory of Open Access Journals (Sweden)

E. Ali

2017-07-01

Full Text Available The effect of different oxygen feeding scenarios in a fixed bed reactor for the production of Maleic anhydride (MA is studied. Two reactor configurations were examined. In the first configuration, a cross flow reactor (CFR with 4 discrete feeding points is considered. Another configuration is the conventional packed-bed reactor (PBR with a single feed. Nonlinear Model Predictive Controller (NLMPC was used as optimal controller to operate the CFR in dynamic mode and to optimize the multiple feed dosages in order to enhance the MA yield. The simulation results indicated that different combinations of the four feed ratios can operate the reactor at the best value for the yield provided the first feeding point is kept as low as possible. For the packed bed reactor configuration, a single oxygen feed is considered and is optimized transiently by NLMPC. The simulation outcomes showed that the reactor performance in terms of the produced MA mole fraction can also be enhanced to the same magnitude obtained by CFR configuration. This improvement requires decreasing the oxygen ratio in the reactor single feed by 70%.

Membrane protein extraction and purification using styrene-maleic acid (SMA) copolymer: effect of variations in polymer structure.

Science.gov (United States)

Morrison, Kerrie A; Akram, Aneel; Mathews, Ashlyn; Khan, Zoeya A; Patel, Jaimin H; Zhou, Chumin; Hardy, David J; Moore-Kelly, Charles; Patel, Roshani; Odiba, Victor; Knowles, Tim J; Javed, Masood-Ul-Hassan; Chmel, Nikola P; Dafforn, Timothy R; Rothnie, Alice J

2016-12-01

The use of styrene-maleic acid (SMA) copolymers to extract and purify transmembrane proteins, while retaining their native bilayer environment, overcomes many of the disadvantages associated with conventional detergent-based procedures. This approach has huge potential for the future of membrane protein structural and functional studies. In this investigation, we have systematically tested a range of commercially available SMA polymers, varying in both the ratio of styrene and maleic acid and in total size, for the ability to extract, purify and stabilise transmembrane proteins. Three different membrane proteins (BmrA, LeuT and ZipA), which vary in size and shape, were used. Our results show that several polymers, can be used to extract membrane proteins, comparably to conventional detergents. A styrene:maleic acid ratio of either 2:1 or 3:1, combined with a relatively small average molecular mass (7.5-10 kDa), is optimal for membrane extraction, and this appears to be independent of the protein size, shape or expression system. A subset of polymers were taken forward for purification, functional and stability tests. Following a one-step affinity purification, SMA 2000 was found to be the best choice for yield, purity and function. However, the other polymers offer subtle differences in size and sensitivity to divalent cations that may be useful for a variety of downstream applications. © 2016 The Author(s); published by Portland Press Limited on behalf of the Biochemical Society.

Carbon Nanotubes Reinforced Maleic Anhydride-Modified Xylan-g-Poly(N-isopropylacrylamide) Hydrogel with Multifunctional Properties

Science.gov (United States)

Liu, Xinxin; Song, Tao; Chang, Minmin; Meng, Ling; Wang, Xiaohui; Sun, Runcang; Ren, Junli

2018-01-01

Introducing multifunctional groups and inorganic material imparts xylan-based hydrogels with excellent properties, such as responsiveness to pH, temperature, light, and external magnetic field. In this work, a composite hydrogel was synthesized by introducing acid treated carbon nanotubes (AT-CNTs) into the maleic anhydride modified xylan grafted with poly(N-isopropylacrylamide) (MAX-g-PNIPAM) hydrogels network. It was found that the addition of AT-CNTs affected the MAX-g-PNIPAM hydrogel structure, the swelling ratio and mechanical properties, and imparted the hydrogel with new properties of electrical conductivity and near infrared region (NIR) photothermal conversion. AT-CNTs could reinforce the mechanical properties of MAX-g-PNIPAM hydrogels, being up to 83 kPa for the compressive strength when the amount was 11 wt %, which was eight times than that of PNIPAM hydrogel and four times than that of MAX-g-PNIPAM hydrogel. The electroconductibility was enhanced by the increase of AT-CNTs amounts. Meanwhile, the composite hydrogel also exhibited multiple shape memory and NIR photothermal conversion properties, and water temperature was increased from 26 °C to 56 °C within 8 min under the NIR irradiation. Thus, the AT-CNTs reinforced MAX-g-PNIPAM hydrogel possessed promising multifunctional properties, which offered many potential applications in the fields of biosensors, thermal-arrest technology, and drug-controlled release. PMID:29495611

A self-crosslinking thermosetting monomer with both epoxy and anhydride groups derived from Tung oil fatty acids: Synthesis and properties

Science.gov (United States)

A self-crosslinking compound with epoxy groups and anhydride groups (GEMA) has been successfully synthesized from Tung oil fatty acid by reacting with maleic anhydride via the Diels-Alder reaction. GEMA has very good storage stability and can be cured with trace amounts of tertiary amine. This advan...

Radiation grafting of styrene and maleic anhydride onto PTFE membranes and sequent sulfonation for applications of vanadium redox battery

International Nuclear Information System (INIS)

Qiu Jingyi; Ni Jiangfeng; Zhai Maolin; Peng Jing; Zhou Henghui; Li Jiuqiang; Wei Genshuan

2007-01-01

Using γ-radiation technique, poly(tetrafluoroethylene) (PTFE) membrane was grafted with styrene (St) (PTFE-graft-PS) or binary monomers of St and maleic anhydride (MAn) (PTFE-graft-PS-co-PMAn), respectively. Then grafted membranes were further sulfonated with chlorosulfonic acid into ion-exchange membranes (denoted as PTFE-graft-PSSA and PTFE-graft-PSSA-co-PMAc, respectively) for application of vanadium redox battery (VRB). Micro-FTIR analysis indicated that PTFE was successfully grafted and sulfonated at the above two different conditions. However, a higher degree of grafting (DOG) was obtained in St/MAn binary system at the same dose due to a synergistic effect. Comparing with PTFE-graft-PSSA, PTFE-graft-PSSA-co-PMAc membrane showed higher water uptake and ion-exchange capacity (IEC) and lower area resistance (AR) at the same DOG. In addition, PTFE-graft-PSSA-co-PMAc with 6% DOG also showed a higher IEC and higher conductivity compared to Nafion membrane. Radiation grafting of PTFE in St/MAn binary system and sequent sulfonation is an appropriate method for preparing ion-exchange membrane of VRB

Amphiphilic graft copolymer based on poly(styrene-co-maleic anhydride) with low molecular weight polyethylenimine for efficient gene delivery

Science.gov (United States)

Duan, Xiaopin; Xiao, Jisheng; Yin, Qi; Zhang, Zhiwen; Mao, Shirui; Li, Yaping

2012-01-01

Background and methods A new amphiphilic comb-shaped copolymer (SP) was synthesized by conjugating poly(styrene-co-maleic anhydride) with low molecular weight polyethyleneimine for gene delivery. Fourier transform infrared spectrum, 1H nuclear magnetic resonance, and gel permeation chromatography were used to characterize the graft copolymer. Results The buffering capability of SP was similar to that of polyethyleneimine within the endosomal pH range. The copolymer could condense DNA effectively to form complexes with a positive charge (13–30 mV) and a small particle size (130–200 nm) at N/P ratios between 5 and 20, and protect DNA from degradation by DNase I. In addition, SP showed much lower cytotoxicity than polyethyleneimine 25,000. Importantly, the gene transfection activity and cellular uptake of SP-DNA complexes were all markedly higher than that of complexes of polyethyleneimine 25,000 and DNA in MCF-7 and MCF-7/ADR cell lines. Conclusion This work highlights the promise of SP as a safe and efficient synthetic vector for DNA delivery. PMID:23028224

Styrene-Assisted Maleic Anhydride Grafted Poly(lactic acid as an Effective Compatibilizer for Wood Flour/Poly(lactic acid Bio-Composites

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Jun Du

2017-11-01

Full Text Available This study aimed to evaluate the effect of styrene-assisted maleic anhydride-grafted poly(lactic acid (PLA-g-St/MAH on the interfacial properties of wood flour/poly(lactic acid (PLA bio-composites. PLA-g-St/MAH was synthesized by free-radical melt grafting using styrene as a comonomer and dicumyl peroxide as an initiator. The structure of PLA-g-St/MAH was characterized by Fourier transform infrared spectroscopy. Wood flour/PLA composites were prepared by compression molding using PLA-g-St/MAH as a compatibilizer. The effects of PLA-g-St/MAH on the rheological and mechanical properties, as well as on the fractured surface morphology of the composites were investigated. Results indicated that storage modulus, complex viscosity, equilibrium torque, and shear heat were significantly increased. The mechanical properties of the wood flour/PLA composites were also significantly increased after the addition of PLA-g-St/MAH. The maximum values were achieved at the loading rate of 3 wt % because of the improved interfacial adhesion between the wood flour and the PLA matrix.

Enhancement of the Mechanical Properties of Basalt Fiber-Wood-Plastic Composites via Maleic Anhydride Grafted High-Density Polyethylene (MAPE Addition

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Yun Lu

2013-06-01

Full Text Available This study investigated the mechanisms, using microscopy and strength testing approaches, by which the addition of maleic anhydride grafted high-density polyethylene (MAPE enhances the mechanical properties of basalt fiber-wood-plastic composites (BF-WPCs. The maximum values of the specific tensile and flexural strengths are achieved at a MAPE content of 5%–8%. The elongation increases rapidly at first and then continues slowly. The nearly complete integration of the wood fiber with the high-density polyethylene upon MAPE addition to WPC is examined, and two models of interfacial behavior are proposed. We examined the physical significance of both interfacial models and their ability to accurately describe the effects of MAPE addition. The mechanism of formation of the Model I interface and the integrated matrix is outlined based on the chemical reactions that may occur between the various components as a result of hydrogen bond formation or based on the principle of compatibility, resulting from similar polarity. The Model I fracture occurred on the outer surface of the interfacial layer, visually demonstrating the compatibilization effect of MAPE addition.

Enhancement of the Mechanical Properties of Basalt Fiber-Wood-Plastic Composites via Maleic Anhydride Grafted High-Density Polyethylene (MAPE) Addition.

Science.gov (United States)

Chen, Jinxiang; Wang, Yong; Gu, Chenglong; Liu, Jianxun; Liu, Yufu; Li, Min; Lu, Yun

2013-06-18

This study investigated the mechanisms, using microscopy and strength testing approaches, by which the addition of maleic anhydride grafted high-density polyethylene (MAPE) enhances the mechanical properties of basalt fiber-wood-plastic composites (BF-WPCs). The maximum values of the specific tensile and flexural strengths are achieved at a MAPE content of 5%-8%. The elongation increases rapidly at first and then continues slowly. The nearly complete integration of the wood fiber with the high-density polyethylene upon MAPE addition to WPC is examined, and two models of interfacial behavior are proposed. We examined the physical significance of both interfacial models and their ability to accurately describe the effects of MAPE addition. The mechanism of formation of the Model I interface and the integrated matrix is outlined based on the chemical reactions that may occur between the various components as a result of hydrogen bond formation or based on the principle of compatibility, resulting from similar polarity. The Model I fracture occurred on the outer surface of the interfacial layer, visually demonstrating the compatibilization effect of MAPE addition.

The properties of poly(lactic acid)/starch blends with a functionalized plant oil: tung oil anhydride.

Science.gov (United States)

Xiong, Zhu; Li, Chao; Ma, Songqi; Feng, Jianxian; Yang, Yong; Zhang, Ruoyu; Zhu, Jin

2013-06-05

Bio-sourced polymers, polylactide (PLA) and starch, have been melt-blended by lab-scale co-extruder with tung oil anhydride (TOA) as the plasticizer. The ready reaction between the maleic anhydride on TOA and the hydroxyl on starch led TOA molecules to accumulate on starch and increased the compatibility of PLA/starch blends, which was confirmed by FT-IR analyses and SEM. The TOA could change the mechanical properties and physical behaviors of PLA/starch blends. DSC and DMA analysis show that the TOA layer on starch has an effect on the thermal behavior of PLA in the ternary blend. The enrichment of TOA on starch improves the toughness and impact strength of the PLA/starch blends. The adding amount of TOA in PLA/starch blends primarily determined the compatibility and mechanical properties of the resulted ternary blends. The tensile and impact fracture modes of the PLA/starch blend with or without TOA has also been investigated by SEM analysis. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

Intranasal Administration of Maleic Anhydride-Modified Human Serum Albumin for Pre-Exposure Prophylaxis of Respiratory Syncytial Virus Infection

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Zhiwu Sun

2015-02-01

Full Text Available Respiratory syncytial virus (RSV is the leading cause of pediatric viral respiratory tract infections. Neither vaccine nor effective antiviral therapy is available to prevent and treat RSV infection. Palivizumab, a humanized monoclonal antibody, is the only product approved to prevent serious RSV infection, but its high cost is prohibitive in low-income countries. Here, we aimed to identify an effective, safe, and affordable antiviral agent for pre-exposure prophylaxis (PrEP of RSV infection in children at high risk. We found that maleic anhydride (ML-modified human serum albumin (HSA, designated ML-HSA, exhibited potent antiviral activity against RSV and that the percentages of the modified lysines and arginies in ML- are correlated with such anti-RSV activity. ML-HSA inhibited RSV entry and replication by interacting with viral G protein and blocking RSV attachment to the target cells, while ML-HAS neither bound to F protein, nor inhibited F protein-mediated membrane fusion. Intranasal administration of ML-HSA before RSV infection resulted in significant decrease of the viral titers in the lungs of mice. ML-HSA shows promise for further development into an effective, safe, affordable, and easy-to-use intranasal regimen for pre-exposure prophylaxis of RSV infection in children at high risk in both low- and high-income countries.

Separation and recovery of lead from a low concentration solution of lead(II) and zinc(II) using the hydrolysis production of poly styrene-co-maleic anhydride

Energy Technology Data Exchange (ETDEWEB)

Liang, Xing; Su, Yibing [College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou (China); Yang, Ying, E-mail: Yangying@lzu.edu.cn [College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou (China); Qin, Wenwu [College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou (China)

2012-02-15

Highlights: Black-Right-Pointing-Pointer Separation and recovery of Pb(II) from a solution of Pb(II) and Zn(II) was performed. Black-Right-Pointing-Pointer Pb(II) can be recovered using the hydrolysis production of poly styrene-co-maleic anhydride. Black-Right-Pointing-Pointer The adsorption capacity of the PSMA resin for Pb(II) is 641.62 mg g{sup -1}. Black-Right-Pointing-Pointer Pb(II) can be recovered through desorption of Pb-PSMA into Pb(II) ion and the solid PSMA resin. Black-Right-Pointing-Pointer The resin can be repeatedly used through desorption by an inorganic acid condition (6 M H{sub 2}SO{sub 4}). - Abstract: The Pb-Zn separation/preconcentration technique, based on the complex formation reaction of Pb(II) and Zn(II), using a copolymer poly(styrene-co-maleic anhydride) (PSMA), without adding any carrier element was developed. The effects of several experimental parameters such as solution pH, temperature and adsorption time were studied. The experimental results show that the PSMA resin-Pb equilibrium was achieved in 2 min and the Pb(II) loading capacity is up to 641.62 mg g{sup -1} in aqueous solution under optimum conditions, which is much higher than the Zn(II) loading capacity within 80 min. The adsorption test for Pb(II) indicates that PSMA can recover Pb(II) from a mixed solution of Pb(II), Zn(II) and light metals such as Ca(II) and Mg(II) with higher adsorption rate and larger selective coefficient. A further study indicates that PSMA as chelating resins recovering Pb(II) can be regenerated via mineral acid (6 M H{sub 2}SO{sub 4}). PSMA was synthesized by radical polymerization and tested as an adsorbent for the selective recovery of Pb(II). In addition, the formation procedure and structure of Pb-PSMA complex were also studied. Both the PSMA and the Pb-PSMA complex were characterized by means of FTIR spectroscopy, elemental analysis, gel permeation chromatography (GPC) and atomic absorption spectrometry (AAS).

Insight into the informational-structure behavior of the Diels-Alder reaction of cyclopentadiene and maleic anhydride.

Science.gov (United States)

Molina-Espíritu, Moyocoyani; Esquivel, Rodolfo O; Kohout, Miroslav; Angulo, Juan Carlos; Dobado, José A; Dehesa, Jesús S; LópezRosa, Sheila; Soriano-Correa, Catalina

2014-08-01

The course of the Diels-Alder reactions of cyclopentadiene and maleic anhydride were studied. Two reaction paths were modelled: endo- and exo-selective paths. All structures within the transient region were characterized and analyzed by means of geometrical descriptors, physicochemical parameters and information-theoretical measures in order to observe the linkage between chemical behavior and the carriage of information. We have shown that the information-theoretical characterization of the chemical course of the reaction is in complete agreement with its phenomenological behavior in passing from reactants to products. In addition, we were able to detect the main differences between the two reaction mechanisms. This type of informational analysis serves to provide tools to help understand the chemical reactivity of the two simplest Diels-Alder reactions, which permits the establishment of a connection between the quantum changes that molecular systems exert along reaction coordinates and standard physicochemical phenomenology. In the present study, we have shown that every reaction stage has a family of subsequent structures that are characterized not solely by their phenomenological behavior but also by informational properties of their electronic density distribution (localizability, order, uniformity). Moreover, we were able to describe the main differences between endo-adduct and exo-adduct pathways. With the advent of new experimental techniques, it is in principle possible to observe the structural changes in the transient regions of chemical reactions. Indeed, through this work we have provided the theoretical concepts needed to unveil the concurrent processes associated with chemical reactions.

Photo- and radiation chemical cycloaddition of maleic acid derivatives to ethylene and acetylene under elavated pressure

International Nuclear Information System (INIS)

Mirbach, M.

1975-01-01

Based on spectroscopic and kinetic measurements the influence of high pressure on some selected photochemical cycloaddition-reactions is studied. The photo-cycloaddition-reaction of maleic acid anhydride with ethylen has been performed under high ethylen pressures ( 90%). Surprisingly the quantum yield of the cyclo aduct decreases with increasing ethylene pressure from PHI = 0.06 at p = 1 bar to PHI = 0.022 at p = 42 bar. Based on Stern-Volmer quenching experiments, the decrease in ring formation with increasing ethylene concentrations could be explained by an endoergic triplet energy transfer from maleic acid anhydride to ethylene. The type II dissociation of butyrophenone has been quenched also with ethylene. With a lifetime for the first excited butyrophenone triplett state of tau = 6.8 x 10 -8 sec, obtained from kinetic data, the velocity constant can be calculated for this reaction with the result k 5 = 3 x 10 6 M -1 sec -1 . (orig./HK) [de

Silver-containing polymer composition used in spacecraft and semiconductor optoelectronics control systems

Energy Technology Data Exchange (ETDEWEB)

Ivanov, A. A., E-mail: alexchemtsu@rambler.ru; Tuev, V. I., E-mail: tvi-retem@main.tusur.ru [Tomsk State University of Control Systems and Radioelectronics, Tomsk, 634050 (Russian Federation)

2015-10-27

The copolymer of the vinyl chloride-maleic anhydride and silver nano- and microparticle (70 wt %) composition is offered as a conductive adhesive for fixing various chips on the dielectric substrate. The wiring volume resistivity is up to 3.1×10{sup −8} Ohm×m. The adhesive strength of the silver-containing polymer composition (70% of Ag) applied under a shear on the dielectric substrate is 106 N/mm{sup 2}. Adhesive layers obtained from these substances have a high thermal conductivity up to λ = 199.93 W/m×K that depends on the amount of Ag in the polymer composition.

Fabrication of Poly(styrene-co-maleic anhydride)@Ag Spheres with High Surface Charge Intensity and their Self-Assembly into Photonic Crystal Films.

Science.gov (United States)

Bi, Jiajie; Fan, Genrui; Wu, Suli; Su, Xin; Xia, Hongbo; Zhang, Shu-Fen

2017-10-01

Herein, we developed a method to prepare monodisperse poly(styrene-co-maleic anhydride)@Ag (PSMA@Ag) core-shell microspheres with high surface charge intensity by using an in situ reduction method. In this method, ethylenediamine tetraacetic acid tetrasodium salt (Na 4 EDTA) was used as a reducing agent to promote the growth of Ag, and at the same time endowed the PSMA@Ag spheres with a surface charge. The monodispersity of PSMA and PSMA@Ag and the ordered array of the photonic crystal films were characterized by using SEM. The formation of Ag nanoparticles was confirmed by using TEM, HR-TEM, and XRD characterizations. Due to the existence of surface charges, the obtained PSMA@Ag microspheres easily self-assembled to form photonic crystal structures. In addition, the surface-enhanced Raman scattering (SERS) activity of the PSMA@Ag photonic crystal films was evaluated by detecting the signal from Raman probe molecules, 4-aminothiophenol (4-ATP). The PSMA@Ag photonic crystal films exhibited a high SERS effect, a low detection limit of up to 10 -8 for 4-ATP, good uniformity, and reproducibility.

Langmuir-Blodgett films prepared from pre-formed cholestanic liquid-crystalline polymers

Energy Technology Data Exchange (ETDEWEB)

Tundo, P.; Hodge, P.; Valli, L.; Davis, F. (Venice Univ. (Italy). Dip. di Scienze Ambientali Lecce Univ. (Italy). Dip. di Scienza dei Materiali Manchester Univ. (United Kingdom). Dep. of Chemistry)

1992-01-01

A series of alternating copolymers of maleic anhydride and a-olefins functionalized through different alkyl chains with cholestanic groups were synthetised and derivatives prepared by reactions of the anhydride residues with methanol, water, dimethylamine and morpholine, respectively. The same starting functionalized a-olefins were used to prepare other suitable compounds in order to correlate the features of the liquid-crystalline behaviour of the mesogenic cholestanic group with the stability of the forthcoming polymeric or not polymeric Langmuir-Blodgett (LB) films. For some copolymers surface pressure against area per molecule isotherms are reported. In some multilayer (LB) films, the spacings between the layers were determined by the detection of BRAGG peaks by X-ray diffraction. The (LB) films of these polymers are closed packed, owing to either the polymeric skeleton or liquid-crystalline interaction.

Adsorption of heavy metal ions and azo dyes by crosslinked nanochelating resins based on poly(methylmethacrylate-co-maleic anhydride

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M. Ghaemy

2014-03-01

Full Text Available Chelating resins are suitable materials for the removal of heavy metals in water treatments. A copolymer, Poly(MMA-co-MA, was synthesized by radical polymerization of maleic anhydride (MA and methyl methacrylate (MMA, characterized and transformed into multifunctional nanochelating resin beads (80–150 nm via hydrolysis, grafting and crosslink reactions. The resin beads were characterized by swelling studies, field emission scanning electron microscopy (FESEM and Fourier transform infrared spectroscopy (FTIR. The main purpose of this work was to determine the adsorption capacity of the prepared resins (swelling ratio ~55% towards metal ions such as Hg2+, Cd2+, Cu2+ from water at three different pH values (3, 6 and 9. Variations in pH and types of metal ions have not significantly affected the chelation capacity of these resins. The maximum chelation capacity of one of the prepared resin beads (Co-g-AP3 for Hg2+ was 63, 85.8 and 71.14 mg/g at pH 3, 6 and 9, respectively. Approximately 96% of the metal ions could be desorbed from the resin. Adsorption capacity of these resins towards three commercial synthetic azo dyes was also investigated. The maximum adsorption of dye AY42 was 91% for the resin Co-g-AP3 at room temperature. This insures the applicability of the synthesized resins for industrial applications.

Syntheses and properties of complex resins obtained by the reaction of polyethyleneimine with maleic anhydride-isobutene copolymer

International Nuclear Information System (INIS)

Usami, Shiro; Hasegawa, Kiyoshi; Takata, Kyoko; Naito, Ryunosuke; Uchida, Hiroshi; Kozuka, Hiroshi.

1985-01-01

Complex resins obtained by the reaction of polyethyleneimine with maleic anhydride-isobutene copolymer around 100 0 C revealed selective ion adsorption depending on the equivalent ratio of nitrogen to carboxyl group (N/COOH). In detail, polyanion-excess complex resins (N/COOH 2+ , Pb 2+ , Zn 2+ and Ni 2+ , and resins containing excess polycation (N/COOH > 1) for metal complex anions such as [CrO 4 ] 2- , [Ag(S 2 O 3 ) 2 ] 3- and [Fe(CN) 6 ] 4- . Furthermore, the polycation-excess complex resins had high adsorption capacity for uranium in solution, for example, a polycationic resin (N/COOH = 1.79) had an adsorption capacity of more than 100 mg U/g-dry base resin in a 75 ppm uranium solution. It also adsorbed and recovered uranium from solution contatining such infinitesimal amounts of uranium as sea water. The results from electron probe X-ray microanalyser (EPMA) of a polycationic resin (N/COOH = 1.79) indicated that cations such as Ca 2+ and Mg 2+ , abundant in sea water, were not adsorbed at all while such anions as Cl - and S 2- were adsorbed. It was found that Br - , I - , etc. were not adsorbed from sea water while these anions were adsorbed from the solutions containing them independently. The result indicated that Cl - in sea water probably interfered the adsorption of Br - , I - , etc. However, uranium was adsorbed from sea water in spite of its extremely low concentration without any disturbance of other co-existing ions. It was found that Ni 2+ and Cu 2+ were also adsorbed. (author)

Low-Cost and High-Impact Environmental Solutions for Military Composite Structures

Science.gov (United States)

2005-12-15

moduli of UPE polymers are considerably increased when neopentyl glycol is used as the polyol instead of ethylene glycol in the formulations [56...general purpose unsaturated polyester based on phthalic anhydride, ethylene glycol , and maleic anhydride. The VIAPAL 570G was a colorless solid in the...modulus. In this case, the neopentyl center of the Bisphenol A backbone of the VE 828 polymer may be responsible for increased modulus values. The

Identifying airway sensitizers: cytokine mRNA profiles induced by various anhydrides

International Nuclear Information System (INIS)

Plitnick, L.M.; Loveless, S.E.; Ladics, G.S.; Holsapple, M.P.; Smialowicz, R.J.; Woolhiser, M.R.; Anderson, P.K.; Smith, C.; Selgrade, M.J.K.

2003-01-01

Exposure to low molecular weight (LMW) chemicals in the workplace has been linked to a variety of respiratory effects. Within the LMW chemicals, one of the major classes involved in these effects are the acid anhydrides. The immunological basis of respiratory hypersensitivity involves CD4+ cells. By virtue of their induction of cytokines typical of CD4+ T-helper type 2 (Th2) cells--interleukin (IL)-4, 10, and 13--respiratory sensitizers may be identified and differentiated from contact sensitizers which induce Th1 cytokines (IL-2 and IFN-γ). Our previous work suggested that the ribonuclease protection assay (RPA) was useful in identifying the respiratory sensitizer, trimellitic anhydride (TMA), based on quantitative differences in Th2 cytokine mRNA as compared to the contact sensitizer dinitrochlorobenzene (DNCB). Therefore, the purpose of the studies described in this report was to expand the chemicals tested in the RPA. To this end, four acid anhydrides with known respiratory sensitization potential, TMA, maleic anhydride (MA), phthalic anhydride (PA) and hexahydrophthalic anhydride (HHPA), were tested. Although previously determined to induce immunologically equivalent responses in a local lymph node assay (LLNA), the initial dose chosen (2.5%) failed to induce Th2 cytokine mRNA expression. To determine if the lack of cytokine expression was related to dose, LLNAs were conducted at higher doses for each of the anhydrides. The highest doses evaluated (four- to six-fold higher than those used in the initial RPA) gave equivalent proliferative responses for the various anhydrides and were used for subsequent RPA testing. At these higher doses, significant increases in Th2 versus Th1 cytokine mRNA were observed for all anhydrides tested. These results suggest that the RPA has the potential to serve as a screen for the detection of LMW airway sensitizing chemicals. However, the basis for selecting immunologically equivalent doses may require some modification

Synthesis of Terpolymers with Homogeneous Composition by Free Radical Copolymerization of Maleic Anhydride, Perfluorooctyl and Butyl or Dodecyl Methacrylates: Application of the Continuous Flow Monomer Addition Technique

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Marian Szkudlarek

2017-11-01

Full Text Available Terpolymers of homogeneous composition were prepared by free radical copolymerization of butyl or dodecyl methacrylate, 1H,1H,2H,2H-perfluorodecyl methacrylate and maleic anhydride using the continuous monomer addition technique. The copolymerization reactions were performed at 65 °C in the presence of azobisisobutyronitrile as an initiator in a mixture of methyl ethyl ketone and 1,3-bis (trifluoromethylbenzene. The monomers and initiator are added to the reaction mixture with the same rate they are consumed in 5- and 10-fold excess compared to the initial monomer stock. The obtained terpolymers with molecular weights Mn = 50,000–70,000 are of uniform composition, close to the composition determined in low conversion experiments, proving the principle of the chosen concept. The kinetic data necessary for the design of the continuous addition experiment were obtained from binary copolymerization experiments at low monomer conversion (to avoid compositional drift. In addition, the so-called terpolymerization parameter was determined from ternary copolymerization experiments.

Water-Soluble Polymers with Strong Photoluminescence through an Eco-Friendly and Low-Cost Route.

Science.gov (United States)

Guo, Zhaoyan; Ru, Yue; Song, Wenbo; Liu, Zhenjie; Zhang, Xiaohong; Qiao, Jinliang

2017-07-01

Photoluminescence (PL) of nonconjugated polymers brings a favorable opportunity for low-cost and nontoxic luminescent materials, while most of them still exhibit relatively weak emission. Strong PL from poly[(maleic anhydride)-alt-(vinyl acetate)] (PMV) from low-cost monomer has been found in organic solvents, yet the necessity of noxious solvents would hinder its practical applications. Herein, through a novel, eco-friendly, and one-step route, PMV-derived PL polymers can be fabricated with the highest quantum yield of 87% among water-soluble nonconjugated PL polymers ever reported. These PMV-derived polymers emit strong blue emission in both solutions and solids, and can be transformed into red-emission agents easily. These PL polymers exhibit application potentials in light-conversion agricultural films. It is assumed that this work not only puts forward a convenient preparation routine for nonconjugated polymers with high PL, but also provides an industrial application possibility for them. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Highly Carboxylated Cellulose Nanofibers via Succinic Anhydride Esterification of Wheat Fibers and Facile Mechanical Disintegration.

Science.gov (United States)

Sehaqui, H; Kulasinski, K; Pfenninger, N; Zimmermann, T; Tingaut, P

2017-01-09

We report herein the preparation of 4-6 nm wide carboxyl-functionalized cellulose nanofibers (CNF) via the esterification of wheat fibers with cyclic anhydrides (maleic, phtalic, and succinic) followed by an energy-efficient mechanical disintegration process. Remarkable results were achieved via succinic anhydride esterification that enabled CNF isolation by a single pass through the microfluidizer yielding a transparent and thick gel. These CNF carry the highest content of carboxyl groups ever reported for native cellulose nanofibers (3.8 mmol g -1 ). Compared to conventional carboxylated cellulose nanofibers prepared via Tempo-mediated oxidation of wheat fibers, the present esterified CNF display a higher molar-mass and a better thermal stability. Moreover, highly carboxylated CNF from succinic anhydride esterification were effectively integrated into paper filters for the removal of lead from aqueous solution and are potentially of interest as carrier of active molecules or as transparent films for packaging, biomedical or electronic applications.

Transparent lithiated polymer films for thermal neutron detection

Energy Technology Data Exchange (ETDEWEB)

Mabe, Andrew N., E-mail: andrew.n.mabe@gmail.com [Department of Chemistry, University of Tennessee, Knoxville, TN 37996 (United States); Auxier, John D. [Department of Chemistry, University of Tennessee, Knoxville, TN 37996 (United States); Urffer, Matthew J. [Department of Nuclear Engineering, University of Tennessee, Knoxville, TN 37996 (United States); Penumadu, Dayakar [Department of Civil and Environmental Engineering, University of Tennessee, Knoxville, TN 37996 (United States); Schweitzer, George K. [Department of Chemistry, University of Tennessee, Knoxville, TN 37996 (United States); Miller, Laurence F. [Department of Nuclear Engineering, University of Tennessee, Knoxville, TN 37996 (United States)

2013-09-11

Novel water-soluble {sup 6}Li loaded copolymer scintillation films have been designed and fabricated to detect thermal neutrons. Styrene and maleic anhydride were copolymerized to form an alternating copolymer, then the anhydride functionality was hydrolyzed using {sup 6}Li hydroxide. The resulting poly(styrene-co-lithium maleate) was mixed with salicylic acid as a fluor and cast as a thin film from water. The maximum {sup 6}Li loading obtained that resulted in a transparent film was 4.36% by mass ({sup 6}Li to polymer). The optimum fluorescence output was obtained for 11.7% salicylic acid by mass, presumably in the form of lithium salicylate, resulting in an optimum film containing 3.85% by mass of {sup 6}Li. A facile and robust synthesis method, film fabrication protocol, photoluminescence results, and scintillation responses are reported herein. -- Highlights: • A transparent polymer scintillator containing 3.85 wt% {sup 6}Li has been synthesized. • This class of polymeric thermal neutron scintillation detector is water-soluble. • Salicylic acid, presumably in the form of lithium salicylate, is used as a fluor. • The material emits 373 photons/α ({sup 241}Am) and an average of 139 photons/β ({sup 36}Cl). • The material emits 360 photons per thermal neutron capture event.

Electrical resistivity and thermal properties of compatibilized multi-walled carbon nanotube/polypropylene composites

Directory of Open Access Journals (Sweden)

A. Szentes

2012-06-01

Full Text Available The electrical resistivity and thermal properties of multi-walled carbon nanotube/polypropylene (MWCNT/PP composites have been investigated in the presence of coupling agents applied for improving the compatibility between the nanotubes and the polymer. A novel olefin-maleic-anhydride copolymer and an olefin-maleic-anhydride copolymer based derivative have been used as compatibilizers to achieve better dispersion of MWCNTs in the polymer matrix. The composites have been produced by extrusion followed by injection moulding. They contained different amounts of MWCNTs (0.5, 2, 3 and 5 wt% and coupling agent to enhance the interactions between the carbon nanotubes and the polymer. The electrical resistivity of the composites has been investigated by impedance spectroscopy, whereas their thermal properties have been determined using a thermal analyzer operating on the basis of the periodic thermal perturbation method. Rheological properties, BET-area and adsorption-desorption isotherms have been determined. Dispersion of MWCNTs in the polymer has been studied by scanning electron microscopy (SEM.

QDs Supported on Langmuir-Blodgett Films of Polymers and Gemini Surfactant

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T. Alejo

2013-01-01

Full Text Available Different LB films of poly(octadecene-co-maleic anhydride, PMAO, poly(styrene-co-maleic anhydride partial 2 butoxy ethyl ester cumene terminated, PS-MA-BEE, and Gemini surfactant ethyl-bis(dimethyl octadecylammonium bromide, 18-2-18, have been used to study the effect of the substrate coating on the surface self-assembly of CdSe quantum dots (QDs. Results show that all the “coating molecules” avoid the 3D aggregation of QDs observed when these nanoparticles are directly deposited on mica. Different morphologies were observed depending on the molecules used as coatings, and this was related to the surface properties, such as wetting ability, and the morphology of the coating LB films.

Epoxy/anhydride thermosets modified with end-capped star polymers with poly(ethyleneimine cores of different molecular weight and poly(ε–caprolactone arms

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C. Acebo

2015-09-01

Full Text Available Multiarm star polymers, with a hyperbranched poly(ethyleneimine (PEI core and poly(ε-caprolactone (PCL arms end-capped with acetyl groups were synthesized by ring-opening polymerization of ε-caprolactone from PEI cores of different molecular weight. These star polymers were used as toughening agents for epoxy/anhydride thermosets. The curing process was studied by calorimetry, thermomechanical analysis and infrared spectroscopy. The final properties of the resulting materials were determined by thermal and mechanical tests. The addition of the star polymers led to an improvement up to 130% on impact strength and a reduction in the thermal stresses up to 55%. The structure and molecular weight of the modifier used affected the morphology of the resulting materials. Electron microscopy showed phase-separated morphologies with nano-sized fine particles well adhered to the epoxy/anhydride matrix when the higher molecular weight modifier was used.

Role of surface functionality on the formation of raspberry-like polymer/silica composite particles: Weak acid–base interaction and steric effect

International Nuclear Information System (INIS)

Wang, Lan; Song, LinYong; Chao, ZhiYin; Chen, PengPeng; Nie, WangYan; Zhou, YiFeng

2015-01-01

Graphical abstract: - Highlights: • Core–shell structured polymer/SiO 2 was obtained with carboxylic-functionalized templates. • Raspberry-like structure was observed with carboxylic and poly(ethylene glycol) hybrid-functionalized polymer microspheres. • Carboxylic groups contributed to the nucleation and the poly(ethylene glycol) chains was used to control the growth of silica particles. • Super-hydrophobic surface was obtained and the contact angle of water on the dual-sized structured surface was up to 160°. - Abstract: The surface functionality of polymer microspheres is the crucial factor to determine the nucleation and growth of silica particles and to construct the organic/inorganic hierarchical structures. The objective of this work was to evaluate the surface functionality and hierarchical morphology relationship via in situ sol–gel reaction. Carboxylic-functionalized poly (styrene-co-maleic anhydride) [P(S-co-MA)], poly(ethylene glycol)-functionalized poly(styrene-co-poly(ethylene glycol) methacrylate) [P(S-co-PEGMA)], and hybrid functionalized poly(styrene-co-maleic anhydride-co-poly(ethylene glycol) methacrylate) [P(S-co-MA-co-PEGMA)] microspheres were synthesized by emulsifier-free polymerization and used as templates. The morphologies of the composite particles were observed by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The results showed that core–shell structure was obtained with P(S-co-MA) as templates; raspberry-like structure was observed by using P(S-co-MA-co-PEGMA) as templates; and no silica particles were attached onto the surface of P(S-co-PEGMA) microspheres. These results indicated that the carboxylic groups on the surface formed by hydrolysis of anhydride groups were the determinate factor to control the nucleation of silica nanoparticles, and the PEG chains on the surface can affect the growth of silica particles. In addition, the particulate films were constructed by assembling these

Plasma deposition of polymer composite films incorporating nanocellulose whiskers

Science.gov (United States)

Samyn, P.; Airoudj, A.; Laborie, M.-P.; Mathew, A. P.; Roucoules, V.

2011-11-01

In a trend for sustainable engineering and functionalization of surfaces, we explore the possibilities of gas phase processes to deposit nanocomposite films. From an analysis of pulsed plasma polymerization of maleic anhydride in the presence of nanocellulose whiskers, it seems that thin nanocomposite films can be deposited with various patterns. By specifically modifying plasma parameters such as total power, duty cycle, and monomer gas pressure, the nanocellulose whiskers are either incorporated into a buckled polymer film or single nanocellulose whiskers are deposited on top of a polymeric film. The density of the latter can be controlled by modifying the exact positioning of the substrate in the reactor. The resulting morphologies are evaluated by optical microscopy, AFM, contact angle measurements and ellipsometry.

The preparation of highly water-soluble multi-walled carbon nanotubes by irreversible noncovalent functionalization with a pyrene-carrying polymer

International Nuclear Information System (INIS)

Xue Chaohua; Zhou Renjia; Shi Minmin; Gao Yan; Wu Gang; Chen Hongzheng; Wang Mang; Zhang Xiaobin

2008-01-01

Multi-walled carbon nanotubes (MWNTs) have been solubilized in water via a noncovalent method of exfoliation and centrifugation cycles with the assistance of hydrolyzed poly(styrene-co-maleic anhydride) carrying pyrene (HPSMAP). After the obtained solution was micro-filtered and dried, a water-soluble complex of HPSMAP-MWNTs was obtained. The solubility of HPSMAP-MWNTs was measured to be 46.2 mg ml -1 with a net MWNT concentration of 7.4 mg ml -1 in water. Thermal gravimetric analyses showed that there was a large amount of polymer remaining on the surface of MWNTs irreversibly after thoroughly removing the free polymer. Other characterizations using transmission electron microscopy, Fourier transform infrared (FTIR) spectroscopy, fluorescence spectra, and fluorescence decay were conducted

Synthesis and Characterization of New ‎Copolymers as Asphalt Additives

Directory of Open Access Journals (Sweden)

Firyal M. ‎ A

2017-12-01

Full Text Available Rheological properties of asphalt S50  were improved by adding different prepared copolymers as additives with high homogeneity of asphalts  samples.  Three types of copolymers were prepared  Poly  (Indene –Co- maleic anhydride(A1 Poly (Acrylonitrile –Co- Maleic anhydride (A2 and Poly (Dipentine –Co-Maleic anhydride (A3, the cross linking of (A3 to (A3d. by using sulfur.              These copolymers  were designed by inserting Maleic anhydride as  rings  containing through backbone of polymer chains to be high potentially to react with water to protect the crack of pavement .And moisture with inhibit bonding of crack of pavement, Many factors should be considered when prepared the additives to enhanced performance to be convenience cost, beneficial thermal safety ,   extended life of the asphalt, preparing conditions which gave high thermal resistance with more stabilities, all these prepared copolymer have been characterized by FTIR and H-NMR spectroscopies .Intrinsic viscosities were calculated. softening point and penetration were observed for all asphalts blends which were  compared with the  asphalt samples, which gave high thermal resistance with more stabilities.                                          The results  showed high properties of these blends when  compared with the original asphalt. The physical properties of a specific polymers are determined by the sequence and chemical structure , When polymers are added to asphalt , the properties of the modified asphalt cement depend on polymer characteristic of asphalt and compatibility of polymer with asphalt. All these prepared copolymers were tested by softening points and penetration for all  asphalt blends which were compared with the asphalt sample. All the Improvements made by adding polymers to asphalt included the Increasing the viscosity of the binder service, the thermal susceptibility of the binder

Structure and thermal performance of poly(styrene-co-maleic anhydride)-g-alkyl alcohol comb-like copolymeric phase change materials

International Nuclear Information System (INIS)

Wang, Haixia; Shi, Haifeng; Qi, Miao; Zhang, Lingjian; Zhang, Xingxiang; Qi, Lu

2013-01-01

Graphical abstract: SMA-g-CnOH comb-like PCMs exhibit the better thermal stability against 1-alcohols due to the protection of SMA backbones, and the degradation temperature is dependent on the side-chain length, where at 5 wt% weight loss T d increased from 193 to 257 °C with n changing from 14 to 26. SMA-g-CnOH PCMs can be widely used under 300 °C for preparation of energy-saving products and materials. - Highlights: • The length of alkyl side-chains determines the thermal energy storage ability. • SMA backbone restricts the crystallization of alkyl side groups. • SMA-g-CnOH PCMs have the better thermal stability against 1-alcohols. - Abstract: A series of comb-like copolymeric phase change materials (SMA-g-CnOH) composed of poly(styrene-co-maleic anhydride) (SMA) and 1-alcohols CnOH with n = 14, 16, 18 or 26, respectively, was synthesized through grafting reaction. The structure and thermal properties of SMA-g-CnOH were investigated by 1 H nuclear magnetic resonance ( 1 H NMR), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and wide-angle X-ray diffraction (WAXD). The DSC analysis indicates that SMA-g-CnOH exhibit good structure stability with phase change enthalpies changing from 37.9 to 110.7 J g −1 . The results showed that the low thermal efficiency of SMA-g-CnOH was ascribed to the small CH 2 segments of side chains participating in the assembled structure of side-chain crystallites. Their advantageous structural stability and thermal performance of SMA-g-CnOH were favorable for phase change materials in the thermal energy storage systems. Additionally, the influence of side-chain length on thermal properties of SMA-g-CnOH also was discussed in detail in combination with the published results

Synthesis and properties of the metallo-supramolecular polymer hydrogel poly[methyl vinyl ether-alt-mono-sodium maleate]·AgNO3: Ag+/Cu2+ ion exchange and effective antibacterial activity

KAUST Repository

Xu, Feng

2014-01-01

The commercial polymeric anhydride poly(methyl vinyl ether-alt-maleic anhydride) (PVM/MA) is converted by reaction with NaOH to give poly(methyl vinyl ether-alt-mono-sodium maleate) (PVM/Na-MA). By addition of AgNO 3-solution, the formation of the silver(i) supramolecular polymer hydrogel poly[methyl vinyl ether-alt-mono-sodium maleate]·AgNO 3 is reported. Freeze-dried samples of the hydrogel show a mesoporous network of polycarboxylate ligands that are crosslinked by silver(i) cations. In the intact hydrogel, ion-exchange studies are reported and it is shown that Ag+ ions can be exchanged by copper(ii) cations without disintegration of the hydrogel. The silver(i) hydrogel shows effective antibacterial activity and potential application as burn wound dressing. © the Partner Organisations 2014.

Synthesis and properties of a novel bio-based polymer from modified soybean oil

Science.gov (United States)

Li, Y. T.; Yang, L. T.; Zhang, H.; Tang, Z. J.

2017-02-01

Maleated acrylated epoxidized soybean oil (MAESO) was prepared by acrylated epoxidized soybean oil (AESO) and maleic anhydride. AESO were obtained by the reaction of epoxidized soybean oil (ESO) with acrylic acid as the ring-opening reagent. The polymer was prepared by MAESO react with styrene. The structures of the products were studied by Fourier transformation infrared spectrometer (FT-IR), and were consistent with the theoretical structures. Swelling experiment indicated that the crosslinking degree increased with increasing epoxy value of ESO. Thermal properties was tested by thermo-gravimetric analysis (TG) and differential scanning calorimetry analysis (DSC), indicating that glass transition temperature (Tg) of the polymer increased with increasing epoxy value of ESO, and thermal stability of polymer have a good correlation with the crosslinking degree. Mechanical properties analysis presented that tensile strength and impact strength affected by epoxy value of ESO. With the increase of epoxy value, the tensile strength increase, while the impact strength decrease. The property of the polymer ranged from elastomer to plastic character depended on the functionality of the ESO.

Controlled release from aspirin based linear biodegradable poly(anhydride esters) for anti-inflammatory activity.

Science.gov (United States)

Dasgupta, Queeny; Movva, Sahitya; Chatterjee, Kaushik; Madras, Giridhar

2017-08-07

This work reports the synthesis of a novel, aspirin-loaded, linear poly (anhydride ester) and provides mechanistic insights into the release of aspirin from this polymer for anti-inflammatory activity. As compared to conventional drug delivery systems that rely on diffusion based release, incorporation of bioactives in the polymer backbone is challenging and high loading is difficult to achieve. In the present study, we exploit the pentafunctional sugar alcohol (xylitol) to provide sites for drug (aspirin) attachment at its non-terminal OH groups. The terminal OH groups are polymerized with a diacid anhydride. The hydrolysis of the anhydride and ester bonds under physiological conditions release aspirin from the matrix. The resulting poly(anhydride ester) has high drug loading (53%) and displays controlled release kinetics of aspirin. The polymer releases 8.5 % and 20%, of the loaded drug in one and four weeks, respectively and has a release rate constant of 0.0035h -0.61 . The release rate is suitable for its use as an anti-inflammatory agent without being cytotoxic. The polymer exhibits good cytocompatibility and anti-inflammatory properties and may find applications as injectable or as an implantable bioactive material. The physical insights into the release mechanism can provide development of other drug loaded polymers. Copyright © 2017 Elsevier B.V. All rights reserved.

Effect of oil palm empty fruit bunches fibers reinforced polymer recycled

Science.gov (United States)

Hermawan, B.; Nikmatin, S.; Sudaryanto; Alatas, H.; Sukaryo, S. G.

2017-07-01

The aim of this research is to process the OPEFB to become fiber with various sizes which will be used as a filler of polymer matrix recycled acrylonitrile butadiene styrene (ABS). Molecular analysis and mechanical test have been done to understand the influence of fiber size toward material capability to receive outer deformation. Single screw extruder formed a biocomposites granular continued with injection moulding to shaped test pieces. Maleic anhydride was added as coupling agent between filler and matrix. Filler concentration were 10 and 20% in fiber size respectively with constant additif. Two kind of fiber glass (10%) were used as comparator. In order to analyze the results of the mechanical test Fisher least significant difference (LSD) in ANOVA method was performed (-with α=0,05-).

Study on thermal properties and crystallization behavior of electron beam irradiated ethylene vinyl acetate (EVA)/waste tyre dust (WTD) blends in the presence of polyethylene graft maleic anhydride (PEgMAH)

Energy Technology Data Exchange (ETDEWEB)

Ramli, Syuhada; Ahmad, S. H. [School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan (Malaysia); Ratnam, C. T. [Radiation Processing Technology Division, Malaysian Nuclear Agency (Nuclear Malaysia), Bangi, 43000 Kajang (Malaysia); Athirah, Nurul [School of Materials and Mineral Resources, USM Engineering Campus (Malaysia)

2013-11-27

The aim of this article is to show the effects of the electron beam irradiation dose and presence of a compatibiliser on the thermal properties and crystallinity of EVA/WTD blends. The purpose of applying electron beam radiation with doses range 50 to 200 kGy and adding a compatibiliser was to enhance the compatibility of the studied blends and at the same time to investigate the possibility of using this technique in the process of recycling polymeric materials. As the compatibilisers, the polyethylene grafted maleic anhydride (PEgMAH) was utilized, they were added at the amounts of 1-5 phr respectively. The enhancement of thermal properties was accompanied by the following effects, discussed in this article: i) an irradiated EVA/WTD blend at 200kGy was found to improve the thermal properties of EVA, ii) the addition of PEgMAH in EVA/WTD blends and the subsequent irradiation allowed prevention of degradation mechanism. iii) the ΔH{sub f} and crystallinity percentage decrease at higher PEgMAH content.

Certain laws governing the influence of high molecular polymer additives on specific electrical conductivity and viscosity of zincate alkaline solution

Energy Technology Data Exchange (ETDEWEB)

Dmitrenko, V.Ye.; Toropetsera, T.N.; Zubov, M.S.

1983-01-01

A study was made of the influence of polymer additives of different nature: polyelectrolyte, copolymer of ethylene with maleic anhydride, polymethacrylic acid and nonpolyectrolyte copolymer of vinyl alcohol with vinyleneglycol and polyvinyleneglycol on specific electrical conductance and viscosity of the zincate alkaline solution. It is indicated that with an increase in the content of additives, the specific conductance of the solution diminishes according to a linear law, while the viscosity rises. The additives of polyelectrolyte nature reduce more strongly the specific conductance and increase the viscosity than the nonpolyelectrolyte additives. From a comparison of the data on specific conductance and viscosity the following conclusion is drawn: the more the polymer ''structures'' the zincate alkaline solution, the more strongly it reduces its specific electrical conductance.

Poly(vinyl methyl ether/maleic anhydride)-Doped PEG-PLA Nanoparticles for Oral Paclitaxel Delivery To Improve Bioadhesive Efficiency.

Science.gov (United States)

Wang, Qian; Li, Chan; Ren, Tianyang; Chen, Shizhu; Ye, Xiaoxia; Guo, Hongbo; He, Haibing; Zhang, Yu; Yin, Tian; Liang, Xing-Jie; Tang, Xing

2017-10-02

Bioadhesive nanoparticles based on poly(vinyl methyl ether/maleic anhydride) (PVMMA) and poly(ethylene glycol) methyl ether-b-poly(d,l-lactic acid) (mPEG-b-PLA) were produced by the emulsification solvent evaporation method. Paclitaxel was utilized as the model drug, with an encapsulation efficiency of up to 90.2 ± 4.0%. The nanoparticles were uniform and spherical in shape and exhibited a sustained drug release compared with Taxol. m-NPs also exhibited favorable bioadhesive efficiency at the same time. Coumarin 6 or DiR-loaded nanoparticles with/without PVMMA (C6-m-NPs/DiR-m-NPs or C6-p-NPs/DiR-p-NPs) were used for cellular uptake and intestinal adhesion experiments, respectively. C6-m-NPs were shown to enhance cellular uptake, and caveolae/lipid raft mediated endocytosis was the primary route for the uptake of the nanoparticles. Favorable bioadhesive efficiency led to prolonged retention in the intestine reflected by the fluorescence in isolated intestines ex vivo. In a ligated intestinal loops model, C6-m-NPs showed a clear advantage for transporting NPs across the mucus layer over C6-p-NPs and free C6. The apparent permeability coefficient (Papp) of PTX-m-NPs through Caco-2/HT29 monolayers was 1.3- and 1.6-fold higher than PTX-p-NPs and Taxol, respectively, which was consistent with the AUC 0-t of different PTX formulations after oral administration in rats. PTX-m-NPs also exhibited a more effective anticancer efficacy, with an IC 50 of 0.2 ± 1.4 μg/mL for A549 cell lines, further demonstrating the advantage of bioadhesive nanoparticles. The bioadhesive nanoparticles m-NPs demonstrated both mucus permeation and epithelial absorption, and thus, this bioadhesive drug delivery system has the potential to improve the bioavailability of drugs that are insoluble in the gastrointestinal environment.

Synthesis, characterization, and assessment of cytotoxic, antiproliferative, and antiangiogenic effects of a novel procainamide hydrochloride-poly(maleic anhydride-co-styrene) conjugate.

Science.gov (United States)

Karakus, Gulderen; Akin Polat, Zubeyde; Sahin Yaglıoglu, Ayse; Karahan, Mesut; Yenidunya, Ali Fazil

2013-01-01

Poly(maleic anhydride-co-styrene) (MAST) was synthesized by a free-radical polymerization reaction. A bioactive molecule, procainamide hydrochloride (PH), was then conjugated to MAST. The conjugation product was named as MAST/PH. Structural characterization of MAST and MAST/PH was carried out by Fourier Transform Infrared and Nuclear Magnetic Resonance spectroscopy. Their molecular weights were determined by size-exclusion chromatography. A mechanism was then suggested for the conjugation reaction. The results of the cytotoxicity assay, employing a mouse fibroblast cell line (L929), indicated that MAST/PH had no cytotoxicity at concentrations [Formula: see text] 62 μg mL(-1) (p > 0.05). Antiproliferative activities of MAST/PH and PH were determined by the BrdU cell proliferation ELISA assay, using C6 and HeLa cell lines. In the experiment, two anticancer chemotherapy drugs, cisplatin and 5-fluorouracil, were included as positive control. Antiproliferative activity results demonstrated that MAST/PH yielded the highest suppression profile (approximately 42%) at 20 μg/ml, while free PH exerted the same activity at 100 μg/ml. Interestingly, both MAST/PH and PH suppressed the proliferation of only one of the cell lines, C6 cells. Both cisplatin and 5-fluorouracil yielded approximately 60% antiproliferative activity on C6 cells at 20 and 100 μg/ml concentrations. Antiangiogenic capacity of both MAST and MAST/PH was also investigated by using the chicken chorioallantoic membrane assay. Results obtained indicated that while MAST/PH could be included into the category of good antiangiogenic substances, the activity score of MAST was within the weak category.

C S Sanmathi

Indian Academy of Sciences (India)

Home; Journals; Bulletin of Materials Science. C S Sanmathi. Articles written in Bulletin of Materials Science. Volume 27 Issue 3 June 2004 pp 243-249 Polymers. Terpolymerization of 2-ethoxy ethylmethacrylate, styrene and maleic anhydride: determination of the reactivity ratios · C S Sanmathi S Prasannakumar B S ...

Retardation of the dewetting process due to the addition of functional copolymers at polymer-polymer interfaces

CERN Document Server

Wunnicke, O; Lorenz-Haas, C; Leiner, V

2002-01-01

We studied the retardation of the dewetting process due to the addition of a functional copolymer in a polymer bilayer film. The model system consists of fully deuterated polystyrene (PS-d) on top of an amorphous polyamide (PA) sublayer on silicon substrates. Bilayer films were prepared with different content (0, 5, 10 and 30 vol. %) of a statistical copolymer (protonated styrene maleic anhydride acid (SMA2) containing 2% MA groups along the chain) being capable of forming hydrogen bonds with PA. The as-prepared as well as the annealed samples were investigated by neutron-reflectivity (NR) experiments, scanning force microscopy and optical microscopy. A significant retardation of dewetting is observed with the addition of SMA2. From model fits of NR curves the scattering length density profiles perpendicular to the sample surface were determined and an enrichment layer of SMA2 is detected. Retardation is explained by the intermixing of SMA2 and PS-d at the interface. (orig.)

Structure and thermal performance of poly(styrene-co-maleic anhydride)-g-alkyl alcohol comb-like copolymeric phase change materials

Energy Technology Data Exchange (ETDEWEB)

Wang, Haixia; Shi, Haifeng, E-mail: haifeng.shi@gmail.com; Qi, Miao; Zhang, Lingjian; Zhang, Xingxiang; Qi, Lu

2013-07-20

Graphical abstract: SMA-g-CnOH comb-like PCMs exhibit the better thermal stability against 1-alcohols due to the protection of SMA backbones, and the degradation temperature is dependent on the side-chain length, where at 5 wt% weight loss T{sub d} increased from 193 to 257 °C with n changing from 14 to 26. SMA-g-CnOH PCMs can be widely used under 300 °C for preparation of energy-saving products and materials. - Highlights: • The length of alkyl side-chains determines the thermal energy storage ability. • SMA backbone restricts the crystallization of alkyl side groups. • SMA-g-CnOH PCMs have the better thermal stability against 1-alcohols. - Abstract: A series of comb-like copolymeric phase change materials (SMA-g-CnOH) composed of poly(styrene-co-maleic anhydride) (SMA) and 1-alcohols CnOH with n = 14, 16, 18 or 26, respectively, was synthesized through grafting reaction. The structure and thermal properties of SMA-g-CnOH were investigated by {sup 1}H nuclear magnetic resonance ({sup 1}H NMR), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and wide-angle X-ray diffraction (WAXD). The DSC analysis indicates that SMA-g-CnOH exhibit good structure stability with phase change enthalpies changing from 37.9 to 110.7 J g{sup −1}. The results showed that the low thermal efficiency of SMA-g-CnOH was ascribed to the small CH{sub 2} segments of side chains participating in the assembled structure of side-chain crystallites. Their advantageous structural stability and thermal performance of SMA-g-CnOH were favorable for phase change materials in the thermal energy storage systems. Additionally, the influence of side-chain length on thermal properties of SMA-g-CnOH also was discussed in detail in combination with the published results.

Separation and recovery of lead from a low concentration solution of lead(II) and zinc(II) using the hydrolysis production of poly styrene-co-maleic anhydride.

Science.gov (United States)

Liang, Xing; Su, Yibing; Yang, Ying; Qin, Wenwu

2012-02-15

The PbZn separation/preconcentration technique, based on the complex formation reaction of Pb(II) and Zn(II), using a copolymer poly(styrene-co-maleic anhydride) (PSMA), without adding any carrier element was developed. The effects of several experimental parameters such as solution pH, temperature and adsorption time were studied. The experimental results show that the PSMA resin-Pb equilibrium was achieved in 2 min and the Pb(II) loading capacity is up to 641.62 mg g(-1) in aqueous solution under optimum conditions, which is much higher than the Zn(II) loading capacity within 80 min. The adsorption test for Pb(II) indicates that PSMA can recover Pb(II) from a mixed solution of Pb(II), Zn(II) and light metals such as Ca(II) and Mg(II) with higher adsorption rate and larger selective coefficient. A further study indicates that PSMA as chelating resins recovering Pb(II) can be regenerated via mineral acid (6M H(2)SO(4)). PSMA was synthesized by radical polymerization and tested as an adsorbent for the selective recovery of Pb(II). In addition, the formation procedure and structure of Pb-PSMA complex were also studied. Both the PSMA and the Pb-PSMA complex were characterized by means of FTIR spectroscopy, elemental analysis, gel permeation chromatography (GPC) and atomic absorption spectrometry (AAS). Copyright © 2011 Elsevier B.V. All rights reserved.

Alternating copolymerization of epoxides with anhydrides initiated by organic bases

Czech Academy of Sciences Publication Activity Database

Hošťálek, Z.; Trhlíková, Olga; Walterová, Zuzana; Martinez, T.; Peruch, F.; Cramail, H.; Merna, J.

2017-01-01

Roč. 88, March (2017), s. 433-447 ISSN 0014-3057 Institutional support: RVO:61389013 Keywords : copolymerization * epoxides * anhydrides Subject RIV: CD - Macromolecular Chemistry OBOR OECD: Polymer science Impact factor: 3.531, year: 2016

Polymer/surfactant assisted self-assembly of nanoparticles into Langmuir–Blodgett films

International Nuclear Information System (INIS)

Alejo, T.; Merchán, M.D.; Velázquez, M.M.; Pérez-Hernández, J.A.

2013-01-01

We studied the ability of poly(octadecene-co-maleic anhydride) (PMAO) and a Gemini surfactant [C 18 H 37 (CH 3 ) 2 N + Br − –(CH 2 ) 2 –N + Br − (CH 3 ) 2 C 18 H 37 ] (18-2-18) to assist in the self-assembly process of CdSe quantum dots (QDs) at the air–water interface. Results show that, while QD agglomeration is generally inhibited by the addition of these components to the Langmuir monolayer of QDs, structure of the film transferred onto mica by the Langmuir–Blodgett method is strongly affected by the dewetting process. Nucleation-and-growth of holes and spinodal-like dewetting were respectively observed in the presence of either PMAO or 18-2-18. When PMAO/18-2-18 mixtures were used, both mechanisms were allowed; nevertheless, even in films prepared with mixtures of low polymer contents, characteristic morphology from the polymer dewetting route prevailed. Highlights: ► Effect of the composition on the LB films of QDs/polymer. ► Effect of the composition on the LB films of QDs/Gemini surfactant. ► Dewetting mechanisms

Crystallo-chemistry of boric anhydride and of anhydrous borates

International Nuclear Information System (INIS)

Bernardin, Jacques

1968-01-01

After an overview of various aspects related to the atomic structure of boron and of its three-bind and four-bind compounds, this report briefly presents the different forms of boric anhydride (in solid, liquid, glassy and gaseous state), presents and comments the structure of these different forms, and addresses the molten boric anhydride which is used as oxide solvent. The next part addresses the structure of anhydrous borates. It presents some generalities on their structure, and describes examples of known structures: dimers, trimers, polymers with a degree higher than three like calcium metaborate, caesium tri-borate, lithium tetraborate, or potassium pentaborate

Preparation of polymer microspheres by radiation-induced polymerization

International Nuclear Information System (INIS)

Naka, Y.; Yamamoto, Y.; Yoshida, Y.; Tagawa, S.

1995-01-01

Cross-liking monomer, diethylene glycol dimethacrylate gives microspheres from organic solution by radiation-induced polymerization. /One of the remarkable result is that the number of the microspheres is not changing during the polymerization. Ethyl methacrylate, maleic anhydride, styrene and acrylamide are used as comonomers. These comonomers give the microspheres in the range of 0 to 0.4 as mol fractions. (author)

Preparation, characterization and thermal properties of styrene maleic anhydride copolymer (SMA)/fatty acid composites as form stable phase change materials

International Nuclear Information System (INIS)

Sari, Ahmet; Alkan, Cemil; Karaipekli, Ali; Onal, Adem

2008-01-01

Fatty acids such as stearic acid (SA), palmitic acid (PA), myristic acid (MA) and lauric acid (LA) are promising phase change materials (PCMs) for latent heat thermal energy storage (LHTES) applications, but high cost is the major drawback of them, limiting their utility area in thermal energy storage. The use of fatty acids as form stable PCMs will increase their feasibilities in practical applications due to the reduced cost of the LHTES system. In this regard, a series of styrene maleic anhydride copolymer (SMA)/fatty acid composites, SMA/SA, SMA/PA, SMA/MA, and SMA/LA, were prepared as form stable PCMs by encapsulation of fatty acids into the SMA, which acts as a supporting material. The encapsulation ratio of fatty acids was as much as 85 wt.% and no leakage of fatty acid was observed even when the temperature of the form stable PCM was over the melting point of the fatty acid in the composite. The prepared form stable composite PCMs were characterized using optic microscopy (OM), viscosimetry and Fourier transform infrared (FT-IR) spectroscopy methods, and the results showed that the SMA was physically and chemically compatible with the fatty acids. In addition, the thermal characteristics such as melting and freezing temperatures and latent heats of the form stable composite PCMs were measured by using the differential scanning calorimetry (DSC) technique, which indicated they had good thermal properties. On the basis of all the results, it was concluded that form stable SMA/fatty acid composite PCMs had important potential for practical LHTES applications such as under floor space heating of buildings and passive solar space heating of buildings by using wallboard, plasterboard or floors impregnated with a form stable PCM due to their satisfying thermal properties, easy preparation in desired dimensions, direct usability without needing additional encapsulation thereby eliminating the thermal resistance caused by the shell and, thus, reducing the cost of

Fatigue mechanisms in unidirectional glass-fibre-reinforced polypropylene

DEFF Research Database (Denmark)

Gamstedt, E.K.; Berglund, L.A.; Peijs, T.

1999-01-01

Polypropylene (PP) and polypropylene modified with maleic anhydride (MA-PP) reinforced by continuous longitudinal glass fibres have been investigated. The most prominent effect of the modification with maleic anhydride in the composite is a stronger fibre/matrix interface. The effects of interfac......Polypropylene (PP) and polypropylene modified with maleic anhydride (MA-PP) reinforced by continuous longitudinal glass fibres have been investigated. The most prominent effect of the modification with maleic anhydride in the composite is a stronger fibre/matrix interface. The effects...... of interfacial strength on fatigue performance and on the underlying micromechanisms have been studied for these composite systems. Tension-tension fatigue tests (R = 0.1) were carried out on 0 degrees glass-fibre/PP and glass-fibre/ MA-PP coupons. The macroscopic fatigue behaviour was characterized in terms...

Decoration of a Poly(methyl vinyl ether-co-maleic anhydride)-Shelled Selol Nanocapsule with Folic Acid Increases Its Activity Against Different Cancer Cell Lines In Vitro.

Science.gov (United States)

Ganassin, Rayane; Souza, Ludmilla Regina de; Py-Daniel, Karen Rapp; Longo, João Paulo Figueiró; Coelho, Janaína Moreira; Rodrigues, Mosar Correa; Jiang, Cheng-Shi; Gu, Jinsong; Morais, Paulo César de; Mosiniewicz-Szablewska, Ewa; Suchocki, Piotr; Báo, Sônia Nair; Azevedo, Ricardo Bentes; Muehlmann, Luis Alexandre

2018-01-01

Due to the low therapeutic index of different chemotherapeutic drugs used for cancer treatment, the development of new anticancer drugs remains an intense field of research. A recently developed mixture of selenitetriacylglycerides, selol, was shown to be active against different cancer cells in vitro. As this compound is highly hydrophobic, it was encapsulated, in a previous study, into poly(methyl vinyl ether-co-maleic anhydride)-shelled nanocapsules in order to improve its dispersibility in aqueous media. Following this line of research, the present report aimed at enhancing the In Vitro activity of the selol nanocapsules against cancerous cells by decorating their surface with folic acid. It is known that several cancer cells overexpress folate receptors. Stable folic acid-decorated selol nanocapsules (SNP-FA) were obtained, which showed to be spherical, with a hydro-dynamic diameter of 364 nm, and zeta potential of -24 mV. In comparison to non-decorated selol nanocapsules, SNP-FA presented higher activity against 4T1, MCF-7 and HeLa cells. Moreover, the decoration of the nanocapsules did not alter their toxicity towards fibroblasts, NIH-3T3 cells. These results show that the decoration with folic acid increased the toxicity of selol nanocapsules to cancer cells. These nanocapsules, besides enabling to disperse selol in an aqueous medium, increased the toxicity of this drug In Vitro, and may be useful to treat cancer in vivo, potentially increasing the specificity of selol towards cancer cells.

Modification of montmorillonite fillers by ionizing radiation

International Nuclear Information System (INIS)

Zimek, Z.; Przybytniak, G.; Nowicki, A.; Mirkowski, K.

2006-01-01

The mineral fillers can be modified by using unsaturated compounds: styrene, methacrylic acid and maleic anhydride (MA), following by irradiation with high energy electron beam. In presented paper the authors have used this method to change properties of bentonite S pecjal , containing about 70% of pure montmorillonite. It has been shown that: (a) the particles obtained in this process can be good fillers for the production of composites; (b) maleic anhydride reacts via anhydride group with active ionic sites of bentonite, forming a salt-like compound. Irradiation with electron beam leads to the breakage of double bond in maleic anhydride and to the production of new organic phases

Synthesis and Properties of the Metallo-Supramolecular Polymer Hydrogel Poly[methyl vinyl ether-alt-mono-sodium maleate]∙AgNO3

KAUST Repository

Al-Dossary, Mona S.

2014-05-01

Gels are a special class of materials which are composed of 3D networks of crosslinked polymer chains that encapsulate liquid/air in the matrix. They can be classified into organogels or hydrogels (organic solvent for organogel and water for hydrogel). For hydrogels that contain metallic elements in the form of ions, the term of metallo-supramolecular polymer hydrogel (MSPHG) is often used. The aim of this project is to develop a kind of new MSPHG and investigate its properties and possible applications. The commercial polymeric anhydride poly(methyl vinyl ether-alt-maleic anhydride) (PVM/MA) is converted by reaction with NaOH to give poly(methyl vinyl ether-alt-monosodium maleate) (PVM/Na-MA). By addition of AgNO3-solution, the formation of the silver(I) supramolecular polymer hydrogel poly[methyl vinyl ether-alt-mono-sodium maleate]∙AgNO3 is obtained. Freeze-dried samples of the hydrogel show a mesoporous network of polycarboxylate ligands that are crosslinked by silver(I) cations. The supercritical CO2 dried silver(I) hydrogel was characterized by FT-IR, SEM-EDAX, TEM, TGA and Physical adsorption (BET) measurements. The intact silver(I) hydrogel was characterized by cryo-SEM. In the intact hydrogel, ion-exchange studies are reported and it is shown that Ag+ ions can be exchanged by copper(II) cations without disintegration of the hydrogel. The silver(I) hydrogel shows effective antibacterial activity and potential application as burn wound dressing.

Controlling Styrene Maleic Acid Lipid Particles through RAFT.

Science.gov (United States)

Smith, Anton A A; Autzen, Henriette E; Laursen, Tomas; Wu, Vincent; Yen, Max; Hall, Aaron; Hansen, Scott D; Cheng, Yifan; Xu, Ting

2017-11-13

The ability of styrene maleic acid copolymers to dissolve lipid membranes into nanosized lipid particles is a facile method of obtaining membrane proteins in solubilized lipid discs while conserving part of their native lipid environment. While the currently used copolymers can readily extract membrane proteins in native nanodiscs, their highly disperse composition is likely to influence the dispersity of the discs as well as the extraction efficiency. In this study, reversible addition-fragmentation chain transfer was used to control the polymer architecture and dispersity of molecular weights with a high-precision. Based on Monte Carlo simulations of the polymerizations, the monomer composition was predicted and allowed a structure-function analysis of the polymer architecture, in relation to their ability to assemble into lipid nanoparticles. We show that a higher degree of control of the polymer architecture generates more homogeneous samples. We hypothesize that low dispersity copolymers, with control of polymer architecture are an ideal framework for the rational design of polymers for customized isolation and characterization of integral membrane proteins in native lipid bilayer systems.

Thermotropic properties of phosphatidylcholine nanodiscs bounded by styrene-maleic acid copolymers.

Science.gov (United States)

Dominguez Pardo, J J; Dörr, J M; Renne, M F; Ould-Braham, T; Koorengevel, M C; van Steenbergen, M J; Killian, J A

2017-11-01

Styrene-maleic acid copolymers (SMA) have been gaining interest in the field of membrane research due to their ability to solubilize membranes into nanodics. The SMA molecules act as an amphipathic belt that surrounds the nanodiscs, whereby the hydrophobic styrene moieties can insert in between the lipid acyl chains. Here we used SMA variants with different styrene-to-maleic acid ratio (i.e. 2:1, 3:1 and 4:1) to investigate how lipid packing in the nanodiscs is affected by the presence of the polymers and how it depends on polymer composition. This was done by analyzing the thermotropic properties of a series of saturated phosphatidylcholines in nanodiscs using laurdan fluorescence and differential scanning calorimetry. In all cases it was found that the temperature of the main phase transition (T m ) of the lipids in the nanodiscs is downshifted and that its cooperativity is strongly reduced as compared to the situation in vesicles. These effects were least pronounced for lipids in nanodiscs bounded by SMA 2:1. Unexpected trends were observed for the calorimetric enthalpy of the transition, suggesting that the polymer itself contributes, possibly by rearranging around the nanodiscs when the lipids adopt the fluid phase. Finally, distinct differences in morphology were observed for nanodiscs at relatively high polymer concentrations, depending on the SMA variant used. Overall, the results suggest that the extent of preservation of native thermodynamic properties of the lipids as well as the stability of the nanodiscs at high polymer concentrations is better for SMA 2:1 than for the other SMA variants. Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.

Calcium carbonate interaction analysis in polypropylene compounds and their impact on the formation of beta crystalline phase of this polymer

International Nuclear Information System (INIS)

Sakahara, Rogerio M.; Hui, Wang S.

2011-01-01

The insertion of calcium carbonate (CaCO 3 ) in polypropylene compound is a thoroughly known technique widely studied in the academic area and in the industry. Its wide application is due, mainly, to increase mechanical properties with low manufacturing cost. These improvements in this polymer make it more versatile and competitive compared to other expensive polymers. In this study, the incorporation of four types of CaCO3 from the same manufacturer were compared and the focus was on the size of this mineral filler. Furthermore, it was analyzed the interaction of graphitized polypropylene with maleic anhydride (PP-g-MA) in the same samples. All these samples were analyzed by WAXS and SEM. The physical properties of tensile strength and impact were also analyzed. It was observed from this study that the smallest CaCO3 produced with PP-g-MA resulted in better physical properties with the formation of a crystalline phase beta, as originally studied by other authors using other raw materials. (author)

Polymer/surfactant assisted self-assembly of nanoparticles into Langmuir–Blodgett films

Energy Technology Data Exchange (ETDEWEB)

Alejo, T.; Merchán, M.D. [Departamento de Química Física, Facultad de Ciencias Químicas, Universidad de Salamanca, Plaza de los Caídos s/n, E-37008 Salamanca (Spain); Velázquez, M.M., E-mail: mvsal@usal.es [Departamento de Química Física, Facultad de Ciencias Químicas, Universidad de Salamanca, Plaza de los Caídos s/n, E-37008 Salamanca (Spain); Pérez-Hernández, J.A. [Centro de Láseres Pulsados Ultraintensos (CLPU), E-37008 Salamanca (Spain)

2013-02-15

We studied the ability of poly(octadecene-co-maleic anhydride) (PMAO) and a Gemini surfactant [C{sub 18}H{sub 37} (CH{sub 3}){sub 2}N{sup +}Br{sup −}–(CH{sub 2}){sub 2}–N{sup +}Br{sup −}(CH{sub 3}){sub 2} C{sub 18}H{sub 37}] (18-2-18) to assist in the self-assembly process of CdSe quantum dots (QDs) at the air–water interface. Results show that, while QD agglomeration is generally inhibited by the addition of these components to the Langmuir monolayer of QDs, structure of the film transferred onto mica by the Langmuir–Blodgett method is strongly affected by the dewetting process. Nucleation-and-growth of holes and spinodal-like dewetting were respectively observed in the presence of either PMAO or 18-2-18. When PMAO/18-2-18 mixtures were used, both mechanisms were allowed; nevertheless, even in films prepared with mixtures of low polymer contents, characteristic morphology from the polymer dewetting route prevailed. Highlights: ► Effect of the composition on the LB films of QDs/polymer. ► Effect of the composition on the LB films of QDs/Gemini surfactant. ► Dewetting mechanisms.

Diclofenac sodium (DS) loaded bioerodible polymer based constructs

Science.gov (United States)

Piras, M.; Chiellini, F.; Nikkola, L.; Ashammakhi, N.; Chiellini, E.

2008-02-01

Pain is a prevalent problem that can raise morbidity of patients. Pain killer releasing biodegradable materials have been developed by using different techniques and biomaterials. The objective of the current study is to evaluate the use of a new bioerodible polymer for release of diclofenac sodium (DS). 1-butanol hemiester poly(maleic anhydride-alt-2-methoxyethyl vinyl ether) (PAM14) was prepared in the university of Pisa and selected as polymer of choice for the study. Polymer solutions of 5-10% (in ethanol or in acetic acid) were prepared, half of them containing 2% DS. The solutions were then electrospun to produce nanomats that were subsequently characterized using SEM. Fiber diameter was 160 nm 1 μm. Increasing polymer concentration increased the size of the fibers but reduced the number of beads (with or without DS). In the specimens obtained from acetic acid solution, the addition of DS resulted in a reduction in fiber diameter and an increase in the inter-bead distance. Corresponding ethanol solutions gave more homogeneous specimens than did acetic acid, having a lower number of beads. With the addition of DS a reduction in fiber diameter was observed for the acetic acid specimens. However, in ethanol, adding DS resulted in increased fiber diameter. Accordingly, it can be concluded that it is feasible to develop electrospun diclofenac releasing bioerodible nanostructures that have potential use in pain management. Their further evaluation is however, needed both in vitro and in vivo.

Synthesis and characterization of the polystyrene - asphaltene graft copolymer BY FT-IR spectroscopy

International Nuclear Information System (INIS)

Leo, Adan Yovani; Salazar Ramiro

2008-01-01

The creation of new polymer compounds to be added to asphalt has drawn considerable attention because these substances have succeeded in modifying the asphalt rheological characteristics and physical properties for the enhancement of its behavior during the time of use. This work explains the synthesis of a new graft copolymer based on an asphalt fraction called asphaltene, modified with maleic anhydride. Polystyrene functionalization is conducted in a parallel fashion in order to obtain polybenzylamine resin with an amine - NH2 free group that reacts with the anhydride graft groups in the asphaltene, thus obtaining the new Polystyrene/Asphaltene graft copolymer

Analisis sifat fisika pemanfaatan pati tandan kosong sawit dan limbah plastik LDPE sebagai bahan pembuatan plastik biodegradabel

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Tengku Rachmi Hidayani

2017-06-01

Full Text Available This research aimed to overcome the issue of plastic packaging waste that accumulates in nature because synthetic polymers cannot be easily unraveled by bacteria. Biodegradable plastics were produced by mixing waste of plastics of the low density polyethylene (LDPE with starch of empty palm fruit bunches, modified with the addition of maleic anhydride as a crosslinking agent. To produce biodegradable plastics, different compositions of LDPE waste, starch of empty palm fruit bunch, maleic anhydride, and benzoyl peroxide were used, namely (90: 10: 1: 1, (80: 20: 1: 1, (70: 30: 1: 1, and (60: 40: 1: 1. Research stages consisted of extraction of starch from palm empty fruit bunch (PEFB; preparation of biodegradable plastic powder with the reflux method and xylene solvents; and making of biodegradable plastics using the press molding method. Based on the results of characterization, it was revealed that the optimum condition was generated by biodegradable plastics with the composition of LDPE waste, starch of empty palm bunches, maleic anhydride, and benzoyl peroxide was equal to 60: 40: 1: 1, which generated the tensile strength value of 6.9410 N/m2, the elongation at break of 3.1875%, the the melting point temperature of 103oC, and the decomposition temperature of 384oC. Besides, the thermal gravimetric test generated a residue of 12.6% and results of the analysis on morphological properties suggested that the starch distributed evenly.

TUNG OIL BASED MONOMER FOR THERMOSETTING POLYMERS: SYNTHESIS, CHARACTERIZATION AND COPOLYMERIZATION WITH STYRENE

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Chengguo Liu,

2011-11-01

Full Text Available A tung oil (TO based monomer for rigid thermosetting polymer was synthesized, characterized, and copolymerized with styrene in this study. Tung oil was alcoholyzed with pentaerythritol (PER to get tung oil pentaerythritol alcoholysis products (TOPER, and the optimized conditions were explored according to the yields of TOPER analyzed by gas chromatography-mass spectrometry (GC-MS. The resulting alcoholysis products were maleinated to form tung oil maleate half ester (TOPERMA, and the reaction conditions were determined by monitoring the reaction extents of TOPER and maleic anhydride (MA with 1HNMR spectroscopy. The TO alcoholysis and maleinization reaction products were characterized by IR, 1HNMR, and electrospray ionization-mass spectrometry (ESI-MS techniques. At last, the TOPERMA mixture was cured with styrene (St, and the initiator tert-butyl peroxy benzoate (TPB. Differential scanning calorimetry (DSC was employed to characterize the curing process. Mechanical properties of the cured TOPERMA/St resin further confirmed the best procedure for the maleinization reaction. The loading of TO reached about 30% weight of the resulting thermosetting polymer. This promising material from renewable resources can be a potential substitution for petroleum products when used as sheet molding compounds.

Synthesis and characterization of functional copolymer/organo-silicate nanoarchitectures through interlamellar complex-radical (coterpolymerization

Directory of Open Access Journals (Sweden)

2008-09-01

Full Text Available The functional copolymers, having a combination of rigid/flexible linkages and an ability of complex-formation with interlayered surface of organo-silicate, and their nanocomposites have been synthesized by interlamellar complex-radical (coterpolymerization of intercalated monomer complexes of maleic anhydride (MA and itaconic acid (IA with dimethyl dodecylamine surface modified montmorillonite (organo-MMT (MA…DMDA-MMT and IA…DMDA-MMT n-butyl methacrylate (BMA and/or BMA/styrene monomer mixtures. The results of nanocomposite structure–composition– property relationship studies indicate that interlamellar complex-formation between anhydride/acid units and surface alkyl amine and rigid/flexible linkage balance in polymer chains are important factors providing the effective intercalation/ exfoliation of the polymer chains into the silicate galleries, the formation of nanostructural hybrids with higher thermal stability, dynamic mechanical behaviour and well dispersed morphology.

Application of β-cyclodextrin polymers in separation of metal ions

International Nuclear Information System (INIS)

Kozlowski, C.A.; Kozlowska, J.

2006-01-01

In the present work the competitive transport of Cu(II), Co(II), Ni(II) and Zn(II) ions through the plasticized immobilized membranes was studied. β-cyclodextrin (β-CD) polymers have been used as macrocyclic ligands for separation of metal ions from dilute aqueous solutions by ion exchange methods, i.e. transport across polymer inclusion membranes and ion flotation process. β-CD polymers were prepared by cross-linking β-CD with alkenyl (nonenyl) succinic anhydride derivatives, phtalic and 3-nitrophtalic anhydride in anhydrous N,N-dimethylformamide (DMF) resulting in formation of Polymer A, B or C, respectively. In he case of cooper(II) flotation results obtained with the use of nonylphenol polyoxyethyl glycol ether as an non-anionic surfactant and β-CD polymers as complexation agent, show that the removal of metal decreases with higher molecular mass of β-CD polymers linked by phtalic or 3-nitrophtalic anhydrides. For both derivatives with pH increase the copper(II) removed increase. The highest flotation removal, i.e. 93% is observed for β-CD polymers synthesized at 100 o C with molar ratio CD : NaH : 3-nitrophtalic anhydride equal to 1 : 7 : 7

Block copolymer assisted self-assembly of nanoparticles into Langmuir–Blodgett films: Effect of polymer concentration

International Nuclear Information System (INIS)

Martín-García, Beatriz; Velázquez, M. Mercedes

2013-01-01

We propose to use the self-assembly ability of a block copolymer to obtain CdSe quantum dots (QDs) structures of different morphology. The methodology proposed consist in transferring mixed Langmuir monolayers of QDs and the polymer poly (styrene-co-maleic anhydride) partial 2 buthoxy ethyl ester cumene terminated, PS-MA-BEE onto mica by the Langmuir–Blodgett (LB) methodology. The morphology of the LB films was analyzed by AFM and TEM measurements. Our results show that it is possible to modulate the self-assembly process by modifying the composition of the mixed Langmuir monolayer precursor of the LB film. The different morphologies are interpreted according to two different dewetting mechanisms, growth of holes and spinodal-like dewetting. The growth of holes dewetting process is driven by gravitatory effects and was observed for LB films obtained by transferring Langmuir monolayer of the smallest elasticity values in which the polymer is in brush conformation. The spinodal dewetting mechanism prevailed when the Langmuir monolayer presents the highest elasticity values. - Graphical abstract: Display Omitted - Highlights: • Effect of the surface composition on the LB films architecture. • QDs/polymer LB films morphology interpreted in terms of dewetting mechanism. • The dewetting mechanism depends on the Langmuir monolayer state

Block copolymer assisted self-assembly of nanoparticles into Langmuir–Blodgett films: Effect of polymer concentration

Energy Technology Data Exchange (ETDEWEB)

Martín-García, Beatriz; Velázquez, M. Mercedes, E-mail: mvsal@usal.es

2013-08-15

We propose to use the self-assembly ability of a block copolymer to obtain CdSe quantum dots (QDs) structures of different morphology. The methodology proposed consist in transferring mixed Langmuir monolayers of QDs and the polymer poly (styrene-co-maleic anhydride) partial 2 buthoxy ethyl ester cumene terminated, PS-MA-BEE onto mica by the Langmuir–Blodgett (LB) methodology. The morphology of the LB films was analyzed by AFM and TEM measurements. Our results show that it is possible to modulate the self-assembly process by modifying the composition of the mixed Langmuir monolayer precursor of the LB film. The different morphologies are interpreted according to two different dewetting mechanisms, growth of holes and spinodal-like dewetting. The growth of holes dewetting process is driven by gravitatory effects and was observed for LB films obtained by transferring Langmuir monolayer of the smallest elasticity values in which the polymer is in brush conformation. The spinodal dewetting mechanism prevailed when the Langmuir monolayer presents the highest elasticity values. - Graphical abstract: Display Omitted - Highlights: • Effect of the surface composition on the LB films architecture. • QDs/polymer LB films morphology interpreted in terms of dewetting mechanism. • The dewetting mechanism depends on the Langmuir monolayer state.

The role of polymer dots on efficiency enhancement of organic solar cells: Improving charge transport property

Science.gov (United States)

Li, Jinfeng; Zhang, Xinyuan; Liu, Chunyu; Li, Zhiqi; He, Yeyuan; Zhang, Zhihui; Shen, Liang; Guo, Wenbin; Ruan, Shengping

2017-07-01

In this work, poly(9,9-dioctylfluorene)-co-(4,7-di-2-thienyl-2,1,3-benzothiadiazole) (PF-5DTBT) and copolymer poly(styrene-co-maleic anhydride) (PSMA) dots were prepared as additive for active layer doping to enhance the power conversion efficiency (PCE) of organic solar cells (OSCs), which based on poly[N-9″-hepta-decanyl-2,7-carbazole-alt-5,5-(4‧,7‧-di-2-thienyl-2‧,1‧,3‧-benzothiadiazole) (PCDTBT) and [6,6]-phenyl C71 butyric acid methyl-ester (PC71BM). A high efficiency of 7.40% was achieved due to increase of short-circuit current (Jsc) and fill factor (FF). The operation mechanism of OSCs doping with polymer dots was investigated, which demonstrated that the efficiency enhancement ascribes to improvement of electrical properties, such as exciton generation, exction dissociation, charge transport, and charge collection.

Preliminary in vivo report on the osteocompatibility of poly(anhydride-co-imides) evaluated in a tibial model.

Science.gov (United States)

Ibim, S E; Uhrich, K E; Attawia, M; Shastri, V R; El-Amin, S F; Bronson, R; Langer, R; Laurencin, C T

1998-01-01

A novel class of polymers with mechanical properties similar to cancellous bone are being investigated for their ability to be used in weight-bearing areas for orthopedic applications. The poly(anhydride-co-imide) polymers based on poly[trimellitylimidoglycine-co-1,6-bis(carboxyphenoxy)hexan e] (TMA-Gly:CPH) and poly[pyromellitylimidoalanine-co-1,6-bis(carboxyphenoxy)hexa ne] (PMA-Ala:CPH) in molar ratios of 30:70 were investigated for osteocompatibility, with effects on the healing of unicortical 3-mm defects in rat tibias examined over a 30-day period. Defects were made with surgical drill bits (3-mm diameter) and sites were filled with poly(anhydride-co-imide) matrices and compared to the control poly(lactic acid-glycolic acid) (PLAGA) (50:50), a well-characterized matrix frequently used in bone regeneration studies, and defects without polymeric implants. At predetermined time intervals (3, 6, 9, 12, 20, and 30 days), animals were sacrificed and tissue histology was examined for bone formation, polymer-tissue interaction, and local tissue response by light microscopy. The studies revealed that matrices of TMA-Gly:CPH and PMA-Ala:CPH produced responses similar to the control PLAGA with tissue compatibility characterized by a mild response involving neutrophils, macrophages, and giant cells throughout the experiment for all matrices studied. Matrices of PLAGA were nearly completely degraded by 21 days in contrast to matrices of TMA-Gly:CPH and PMA-Ala:CPH that displayed slow erosion characteristics and maintenance of shape. Defects in control rats without polymer healed by day 12, defects containing PLAGA healed after 20 days, and defects containing poly(anhydride-co-imide) matrices produced endosteal bone growth as early as day 3 and formed bridges of cortical bone around matrices by 30 days. In addition, there was marrow reconstitution at the defect site for all matrices studied along with matured bone-forming cells. This study suggests that novel poly(anhydride

Two Players Make a Formidable Combination: In Situ Generated Poly(acrylic anhydride-2-methyl-acrylic acid-2-oxirane-ethyl ester-methyl methacrylate) Cross-Linking Gel Polymer Electrolyte toward 5 V High-Voltage Batteries.

Science.gov (United States)

Ma, Yue; Ma, Jun; Chai, Jingchao; Liu, Zhihong; Ding, Guoliang; Xu, Gaojie; Liu, Haisheng; Chen, Bingbing; Zhou, Xinhong; Cui, Guanglei; Chen, Liquan

2017-11-29

Electrochemical performance of high-voltage lithium batteries with high energy density is limited because of the electrolyte instability and the electrode/electrolyte interfacial reactivity. Hence, a cross-linking polymer network of poly(acrylic anhydride-2-methyl-acrylic acid-2-oxirane-ethyl ester-methyl methacrylate) (PAMM)-based electrolyte was introduced via in situ polymerization inspired by "shuangjian hebi", which is a statement in a traditional Chinese Kungfu story similar to the synergetic effect of 1 + 1 > 2. A poly(acrylic anhydride) and poly(methyl methacrylate)-based system is very promising as electrolyte materials for lithium-ion batteries, in which the anhydride and acrylate groups can provide high voltage resistance and fast ionic conductivity, respectively. As a result, the cross-linking PAMM-based electrolyte possesses a significant comprehensive enhancement, including electrochemical stability window exceeding 5 V vs Li + /Li, an ionic conductivity of 6.79 × 10 -4 S cm -1 at room temperature, high mechanical strength (27.5 MPa), good flame resistance, and excellent interface compatibility with Li metal. It is also demonstrated that this gel polymer electrolyte suppresses the negative effect resulting from dissolution of Mn 2+ ions at 25 and 55 °C. Thus, the LiNi 0.5 Mn 1.5 O 4 /Li and LiNi 0.5 Mn 1.5 O 4 /Li 4 Ti 5 O 12 cells using the optimized in situ polymerized cross-linking PAMM-based gel polymer electrolyte deliver stable charging/discharging profiles and excellent rate performance at room temperature and even at 55 °C. These findings suggest that the cross-linking PAMM is an intriguing candidate for 5 V class high-voltage gel polymer electrolyte toward high-energy lithium-on batteries.

Adsorption of quantum dots onto polymer and Gemini surfactant films: a quartz crystal microbalance study.

Science.gov (United States)

Alejo, T; Merchán, M D; Velázquez, M M

2014-08-26

We used quartz crystal microbalance with dissipation to study the mechanical properties, the kinetics of adsorption, and the amount of CdSe quantum dots (QDs) adsorbed onto a SiO2 sensor, referred as bare sensor, onto the sensor modified with a film of the polymer poly(maleic anhydride-alt-1-octadecene), PMAO, or with a film of the Gemini surfactant ethyl-bis(dimethyl octadecyl ammonium bromide), abbreviated as 18-2-18. Results showed that when the sensor is coated with polymer or surfactant molecules, the coverage increases compared with that obtained for the bare sensor. On the other hand, rheological properties and kinetics of adsorption of QDs are driven by QD nanoparticles. Thus, the QD films present elastic behavior, and the elasticity values are independent of the molecule used as coating and similar to the elasticity value obtained for QDs films on the bare sensor. The QD adsorption is a two-step mechanism in which the fastest process is attributed to the QD adsorption onto the solid substrate and the slowest one is ascribed to rearrangement movements of the nanoparticles adsorbed at the surface.

Production of polymer composites by radiation and chemical treatments from recycled plastic wastes and their applications

International Nuclear Information System (INIS)

Khaffaga, M.R.A.

2009-01-01

Different applied methods have been proposed for the recycling of poly (ethylene terephthalate)(PET) and its blends with other polymers to obtain useful products. These methods are based on blending with different polymers or compounding with radiation synthesized copolymers based on maleic anhydride with methyl methacrylate, styrene and vinyl acetate. On the other hand, the methods proposed to improve the miscibility of mixed polymers are based on different methods of gamma and electron beam irradiation at various doses (30-50 kGy). Also , the addition of compatibilizers based on LDPE graft copolymer with comonomer composed of ethylene glycol (EG) and acrylic acid (AAc) as well as radiation synthesized copolymer based on acrylic acid and styrene (Sty) monomers during mixing. The modified properties were characterized by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), mechanical testing and studying the affinity for acid, based and disperse dyes. Based on the results obtained throughout this work, few conclusions may made:(1) The composites of PET with copolymers is effective than the blending with other polymers. (2) The pre method of gamma or electron beam irradiation is effectively improved the miscibility of PET/LDPE or PET/PS blends than the direct method of irradiation.(3) The addition of EG/AAc or AAc/Sty copolymers during mixing improved the miscibility than the use of graft copolymer.

Micelles Formed by Polypeptide Containing Polymers Synthesized Via N-Carboxy Anhydrides and Their Application for Cancer Treatment

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Dimitrios Skoulas

2017-06-01

Full Text Available The development of multifunctional polymeric materials for biological applications is mainly guided by the goal of achieving the encapsulation of pharmaceutical compounds through a self-assembly process to form nanoconstructs that control the biodistribution of the active compounds, and therefore minimize systemic side effects. Micelles are formed from amphiphilic polymers in a selective solvent. In biological applications, micelles are formed in water, and their cores are loaded with hydrophobic pharmaceutics, where they are solubilized and are usually delivered through the blood compartment. Even though a large number of polymeric materials that form nanocarrier delivery systems has been investigated, a surprisingly small subset of these technologies has demonstrated potentially curative preclinical results, and fewer have progressed towards commercialization. One of the most promising classes of polymeric materials for drug delivery applications is polypeptides, which combine the properties of the conventional polymers with the 3D structure of natural proteins, i.e., α-helices and β-sheets. In this article, the synthetic pathways followed to develop well-defined polymeric micelles based on polypeptides prepared through ring-opening polymerization (ROP of N-carboxy anhydrides are reviewed. Among these works, we focus on studies performed on micellar delivery systems to treat cancer. The review is limited to systems presented from 2000–2017.

α-Costic anhydride

Directory of Open Access Journals (Sweden)

Moha Berraho

2010-03-01

Full Text Available The title compound [systematic name: 2-(4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-ylacrylic acid anhydride], C30H42O3, is a new isocostic anhydride which was synthesized from the aerial part of Inula Viscosa (L Aiton [or Dittrichia Viscosa (L Greuter]. The molecule adopts an essentially linear shape with two terminal fused-rings bridged by the anhydride group. The external rings have the same conformation (half-chair while each of the two inner rings has an almost ideal chair conformation. In the crystal, intermolecular C—H...O interactions link the molecules into a two-dimensional array in the bc plane.

Dynamic mechanical analysis of binary and ternary polymer blends based on nylon copolymer/EPDM rubber and EPM grafted maleic anhydride compatibilizer

Directory of Open Access Journals (Sweden)

2007-10-01

Full Text Available The dynamic mechanical properties such as storage modulus, loss modulus and damping properties of blends of nylon copolymer (PA6,66 with ethylene propylene diene (EPDM rubber was investigated with special reference to the effect of blend ratio and compatibilisation over a temperature range –100°C to 150°C at different frequencies. The effect of change in the composition of the polymer blends on tanδ was studied to understand the extent of polymer miscibility and damping characteristics. The loss tangent curve of the blends exhibited two transition peaks, corresponding to the glass transition temperature (Tg of individual components indicating incompatibility of the blend systems. The morphology of the blends has been examined by using scanning electron microscopy. The Arrhenius relationship was used to calculate the activation energy for the glass transition of the blends. Finally, attempts have been made to compare the experimental data with theoretical models.

Amide side chain amphiphilic polymers disrupt surface established bacterial bio-films and protect mice from chronic Acinetobacter baumannii infection.

Science.gov (United States)

Uppu, Divakara S S M; Samaddar, Sandip; Ghosh, Chandradhish; Paramanandham, Krishnamoorthy; Shome, Bibek R; Haldar, Jayanta

2016-01-01

Bacterial biofilms represent the root-cause of chronic or persistent infections in humans. Gram-negative bacterial infections due to nosocomial and opportunistic pathogens such as Acinetobacter baumannii are more difficult to treat because of their inherent and rapidly acquiring resistance to antibiotics. Due to biofilm formation, A. baumannii has been noted for its apparent ability to survive on artificial surfaces for an extended period of time, therefore allowing it to persist in the hospital environment. Here we report, maleic anhydride based novel cationic polymers appended with amide side chains that disrupt surface established multi-drug resistant A. baumannii biofilms. More importantly, these polymers significantly (p polymers also show potent antibacterial efficacy against methicillin resistant Staphylococcus aureus (MRSA), vancomycin resistant Enterococci (VRE) and multi-drug resistant clinical isolates of A. baumannii with minimal toxicity to mammalian cells. We observe that optimal hydrophobicity dependent on the side chain chemical structure of these polymers dictate the selective toxicity to bacteria. Polymers interact with the bacterial cell membranes by causing membrane depolarization, permeabilization and energy depletion. Bacteria develop rapid resistance to erythromycin and colistin whereas no detectable development of resistance occurs against these polymers even after several passages. These results suggest the potential use of these polymeric biomaterials in disinfecting biomedical device surfaces after the infection has become established and also for the topical treatment of chronic bacterial infections. Copyright © 2015 Elsevier Ltd. All rights reserved.

Responsive copolymers for enhanced petroleum recovery. Second annual report

Energy Technology Data Exchange (ETDEWEB)

McCormick, C.; Hester, R.

1995-05-01

The authors describe second year efforts in synthesis, characterization, and rheology to develop polymers with significantly improved efficiency in mobility control and conformance. These advanced polymer systems would maintain high viscosities or behave as virtual gels under low shear conditions and at elevated electrolyte concentrations. At high fluid shear rates, associates would deaggregate yielding low viscosity solutions, reducing problems of shear degradation or face plugging during injection. Polymeric surfactants were also developed with potential for use in higher salt, higher temperature reservoirs for mobilization of entrapped oil. Chapters include: Ampholytic terpolymers of acrylamide with sodium 3-acrylamido-3-methylbutanoate and 2-acrylamido-2-methylpropanetrimethylammonium chloride; Hydrophilic sulfobetaine copolymers of acrylamide and 3-(2-acrylamido-methylpropane-dimethylammonio)-1-propanesulfonate; Copolymerization of maleic anhydride and N-vinylformamide; Reactivity ratio of N-vinylformamide with acrylamide, sodium acrylate, and n-butyl acrylate; Effect of the distribution of the hydrophobic cationic monomer dimethyldodecyl(2-acrylamidoethyl)ammonium bromide on the solution behavior of associating acrylamide copolymers; Effect of surfactants on the solution properties of amphipathic copolymers of acrylamide and N,N-dimethyl-N-dodecyl-N-(2-acrylamidoethyl)ammonium bromide; Associative interactions and photophysical behavior of amphiphilic terpolymers prepared by modification of maleic anhydride/ethyl vinyl ether copolymers; Copolymer compositions of high-molecular-weight functional acrylamido water-soluble polymers using direct-polarization magic-angle spinning {sup 13}C NMR; Use of factorial experimental design in static and dynamic light scattering characterization of water soluble polymers; and Porous medium elongational rheometer studies of NaAMB/AM copolymer solutions.

Radiation-induced trioxane postpolymerization in the liquid phase

International Nuclear Information System (INIS)

Kapustina, I.B.; Starchenko, T.V.

1979-01-01

Radiation-induced trioxane postpolymerization in the presence of maleic anhydride and different solvents in the liquid phase has been studied. It has been found that addition of small quantities of different solvents inhibits the trioxane polymerization process both in the presence of maleic anhydride and in the absence of it. Trioxane postpolymerization in a solvent-nonsolvent mixture gives fibrous polyoxymethylene with high molecular mass and high yield

Influence of Temperature on the Colloidal Stability of Polymer-Coated Gold Nanoparticles in Cell Culture Media.

Science.gov (United States)

Zyuzin, Mikhail V; Honold, Tobias; Carregal-Romero, Susana; Kantner, Karsten; Karg, Matthias; Parak, Wolfgang J

2016-04-06

The temperature-dependence of the hydrodynamic diameter and colloidal stability of gold-polymer core-shell particles with temperature-sensitive (poly(N-isopropylacrylamide)) and temperature-insensitive shells (polyallylaminine hydrochloride/polystyrensulfonate, poly(isobutylene-alt-maleic anhydride)-graft-dodecyl) are investigated in various aqueous media. The data demonstrate that for all nanoparticle agglomeration, i.e., increase in effective nanoparticle size, the presence of salts or proteins in the dispersion media has to be taken into account. Poly(N-isopropylacrylamide) coated nanoparticles show a reversible temperature-dependent increase in size above the volume phase transition of the polymer shell when they are dispersed in phosphate buffered saline or in media containing protein. In contrast, the nanoparticles coated with temperature-insensitive polymers show a time-dependent increase in size in phosphate buffered saline or in medium containing protein. This is due to time-dependent agglomeration, which is particularly strong in phosphate buffered saline, and induces a time-dependent, irreversible increase in the hydrodynamic diameter of the nanoparticles. This demonstrates that one has to distinguish between temperature- and time-induced agglomerations. Since the size of nanoparticles regulates their uptake by cells, temperature-dependent uptake of thermosensitive and non-thermosensitive nanoparticles by cells lines is compared. No temperature-specific difference between both types of nanoparticles could be observed. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Poly(anhydride-co-imides): in vivo biocompatibility in a rat model.

Science.gov (United States)

Ibim, S M; Uhrich, K E; Bronson, R; El-Amin, S F; Langer, R S; Laurencin, C T

1998-05-01

The degradation and tissue compatibility characteristics of a novel class of biodegradable poly(anhydride-co-imide) polymers: poly[trimellitylimidoglycine-co-1,6-bis(carboxyphenoxy)hexan e] (TMA-gly: CPH) (in 10:90; 30:70 and 50: 50 molar ratios) and poly[pyromellitylimidoalanine-co-1,6-bis(carboxyphenoxy)hexa ne] (PMA-ala:CPH) (in 10:90 and 30:70 molar ratios) were investigated and compared with control poly(lactic acid/glycolic acid) (PLAGA in 50:50 molar ratio) matrices, a well-characterized biocompatible polymer, in rat subcutaneous tissues for 60 days. Polymers were compression-molded into circular discs of 14 mm x 1 mm in diameter. On post-operative days 7, 14, 28 and 60, histological tissue samples were removed, prepared by fixation and staining, and analyzed by light microscopy. PLAGA matrices produced mild inflammatory reactions and were completely degraded at the end of 60 days, leaving implant tissues that were similar to surgical wounds without implants. TMA-gly:CPH (10:90 and 30:70) matrices produced mild inflammatory reactions by the end of 60 days, similar to those seen with PLAGA. TMA-gly: CPH (50: 50) produced moderate inflammatory reactions characterized by macrophages and edema. PMA-ala:CPH matrices elicited minimal inflammatory reactions that were characterized by fibrous encapsulation by the end of 60 days. In vivo degradation rates of poly(anhydride-co-imides) were similar to PLAGA. Both PMA-ala:CPH and TMA-gly: CPH matrices maintained their shapes and degraded at a constant rate over the period of two months. These polymers, possessing good mechanical properties and tissue compatibility, may be useful in weight-bearing applications in bone.

nanohybrid composites as antimicrobial, antifungal and anticancer platforms

Directory of Open Access Journals (Sweden)

D. Demircan

2018-08-01

Full Text Available This work presents a new approach to synthesize the colloidal ODA-MMT-poly(maleic anhydride-alt-1-dodecene-g-α,ω-methoxyhydroxyl-PEO/silver nanoparticles (AgNPs nanohybrid composites (NHC using the following synthetic pathways: (1 complex-radical alternating copolymerization of maleic anhydride with 1-dodecene α-olefin comonomer, (2 grafting of PEO onto alternating copolymer through esterification, (3 intercalating a copolymer-g-PEO between organoclay layers via complex formation of maleate carboxyl with octadecyl amine, and (4 in situ generation of AgNPs in polymer nanocomposite by annealing method under vacuum. The obtained multifunctional NHCs with different contents of AgNPs were characterized by UV spectroscopy, ζ-potential and size analysis methods. It was demonstrated that annealing of the colloidal NHC is accompanied with in situ generation of stable and partially protonated AgNPs due to specific reducing and stabilizing effects of multifunctional matrix polymer contained positively charged reactive and bioactive sites. Antibacterial and antifungal activities against Gram-negative and Gram-positive bacteria and fungal microorganism were investigated. The cytotoxic, apoptotic and necrotic effects in NHC/L929 fibroblast cells systems were evaluated. The synthesized watersoluble, biocompatible, and bioactive colloidal NHCs are promising candidate for a wide-range of applications in air filtration, food packaging systems, bioengineering, especially in tissue regeneration and nanomedicine.

Effect of modified polypropylene on the interfacial bonding of polymer–aluminum laminated films

International Nuclear Information System (INIS)

Liang, Chang-Sheng; Lv, Zhong-Fei; Bo, Yang; Cui, Jia-Yang; Xu, Shi-Ai

2015-01-01

Highlights: • Aluminium-polymer composite packing material with high T-peel strength was prepared. • Polypropylene was grafted by acrylic acid, glycidyl methacrylate, maleic anhydride. • Grafted polypropylene greatly improved the T-peel strength. • Chemical bonding plays an important role in improving the adhesion strength. - Abstract: The interfacial bonding between functionalized polymers and chromate–phosphate treated aluminum (Al) foil were investigated in this study. Glycidyl methacrylate (GMA), acrylic acid (AA) and maleic anhydride (MAH) were grafted onto polypropylene (PP) to improve its adhesion strength with the treated Al foil. The interfacial peel strength was evaluated by the T-peel test, and the results showed that modification of PP resulted in a significant improvement in the interfacial peel strength from 1 N/15 mm for pure PP to 10–14 N/15 mm for the modified PP. The surface chemistry, topography and surface energy of the modified PP and Al foil after peeling were characterized by time-of-flight secondary ion mass spectrometry (TOF-SIMS), X-ray photoelectron spectroscopy (XPS), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM) and contact angle measurement. The treated Al foil could react with the functional groups of PP, resulting in the formation of new carboxylates. The new chemical bonding rather than the mechanical interlocking contributed to the improvement of adhesion strength

Improved removal of malachite green from aqueous solution using chemically modified cellulose by anhydride.

Science.gov (United States)

Zhou, Yanmei; Min, Yinghao; Qiao, Han; Huang, Qi; Wang, Enze; Ma, Tongsen

2015-03-01

Cellulose modified with maleic (M) and phthalic (P) anhydride, to be named CMA and CPA, were tested as feasible adsorbents for the removal of malachite green from aqueous solution. At the same time, the uptake ability of natural cellulose was also studied for comparison. The structure of material was characterized by FT-IR and XRD. The effects of solution pH, initial dye concentration, contact time and temperature were investigated in detail by batch adsorption experiments. The kinetic and isotherm studies suggested that the adsorption followed the pseudo-second-order model and Langmuir isotherm. The maximum adsorption capacity on CMA and CPA were 370 mg g(-1) and 111 mg g(-1), respectively. Furthermore, the thermodynamics studies indicated the spontaneous nature of adsorption of malachite green on adsorbents. All the studied results showed that the modified cellulose could be used as effective adsorption material for the removal of malachite green from aqueous solutions. Copyright © 2014 Elsevier B.V. All rights reserved.

Synthesis and Verification of Biobased Terephthalic Acid from Furfural

Science.gov (United States)

Tachibana, Yuya; Kimura, Saori; Kasuya, Ken-Ichi

2015-02-01

Exploiting biomass as an alternative to petrochemicals for the production of commodity plastics is vitally important if we are to become a more sustainable society. Here, we report a synthetic route for the production of terephthalic acid (TPA), the monomer of the widely used thermoplastic polymer poly(ethylene terephthalate) (PET), from the biomass-derived starting material furfural. Biobased furfural was oxidised and dehydrated to give maleic anhydride, which was further reacted with biobased furan to give its Diels-Alder (DA) adduct. The dehydration of the DA adduct gave phthalic anhydride, which was converted via phthalic acid and dipotassium phthalate to TPA. The biobased carbon content of the TPA was measured by accelerator mass spectroscopy and the TPA was found to be made of 100% biobased carbon.

Calcium carbonate interaction analysis in polypropylene compounds and their impact on the formation of beta crystalline phase of this polymer; Analise da interacao de diferentes tipos de carbonato de calcio em compositos de polipropileno e suas consequencias na formacao da fase cristalina beta do PP

Energy Technology Data Exchange (ETDEWEB)

NONE

2011-07-01

The insertion of calcium carbonate (CaCO{sub 3}) in polypropylene compound is a thoroughly known technique widely studied in the academic area and in the industry. Its wide application is due, mainly, to increase mechanical properties with low manufacturing cost. These improvements in this polymer make it more versatile and competitive compared to other expensive polymers. In this study, the incorporation of four types of CaCO3 from the same manufacturer were compared and the focus was on the size of this mineral filler. Furthermore, it was analyzed the interaction of graphitized polypropylene with maleic anhydride (PP-g-MA) in the same samples. All these samples were analyzed by WAXS and SEM. The physical properties of tensile strength and impact were also analyzed. It was observed from this study that the smallest CaCO3 produced with PP-g-MA resulted in better physical properties with the formation of a crystalline phase beta, as originally studied by other authors using other raw materials. (author)

Trypsin immobilization in ordered porous polymer membranes for effective protein digestion

International Nuclear Information System (INIS)

Qiao, Juan; Kim, Jin Yong; Wang, Yuan Yuan; Qi, Li; Wang, Fu Yi; Moon, Myeong Hee

2016-01-01

Fast and effective protein digestion is a vital process for mass spectrometry (MS) based protein analysis. This study introduces a porous polymer membrane enzyme reactor (PPMER) coupled to nanoflow liquid chromatography-tandem MS (nLC-ESI-MS/MS) for on-line digestion and analysis of proteins. Poly (styrene-co-maleic anhydride) (PS-co-MAn) was fabricated by the breath figure method to make a porous polymer membrane in which the MAn group was covalently bound to enzyme. Based on this strategy, microscale PPMER (μPPMER) was constructed for on-line connection with the nLC-ESI-MS/MS system. Its capability for enzymatic digestion with bovine serum albumin (BSA) was evaluated with varied digestion periods. The on-line proteolysis of BSA and subsequent analysis with μPPMER-nLC-ESI-MS/MS revealed that peptide sequence coverage increased from 10.3% (digestion time 10 min) to 89.1% (digestion time 30 min). μPPMER can efficiently digest proteins due to the microscopic confinement effect, showing its potential application in fast protein identification and protease immobilization. Applications of on-line digestion using μPPMER with human plasma and urinary proteome samples showed that the developed on-line method yielded equivalent or better performance in protein coverage and identified more membrane proteins than the in-solution method. This may be due to easy accommodation of hydrophobic membrane proteins within membrane pores. - Highlights: • A porous polymer membrane enzyme reactor was developed. • Breath figure method was used for the fabrication of porous polymer membrane. • The enzyme reactor was coupled to nLC-ESI-MS/MS for proteins on-line digestion.

Trypsin immobilization in ordered porous polymer membranes for effective protein digestion

Energy Technology Data Exchange (ETDEWEB)

Qiao, Juan [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Kim, Jin Yong [Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seoul 120-749 (Korea, Republic of); Wang, Yuan Yuan [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Qi, Li, E-mail: qili@iccas.ac.cn [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Wang, Fu Yi [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Moon, Myeong Hee, E-mail: mhmoon@yonsei.ac.kr [Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seoul 120-749 (Korea, Republic of)

2016-02-04

Fast and effective protein digestion is a vital process for mass spectrometry (MS) based protein analysis. This study introduces a porous polymer membrane enzyme reactor (PPMER) coupled to nanoflow liquid chromatography-tandem MS (nLC-ESI-MS/MS) for on-line digestion and analysis of proteins. Poly (styrene-co-maleic anhydride) (PS-co-MAn) was fabricated by the breath figure method to make a porous polymer membrane in which the MAn group was covalently bound to enzyme. Based on this strategy, microscale PPMER (μPPMER) was constructed for on-line connection with the nLC-ESI-MS/MS system. Its capability for enzymatic digestion with bovine serum albumin (BSA) was evaluated with varied digestion periods. The on-line proteolysis of BSA and subsequent analysis with μPPMER-nLC-ESI-MS/MS revealed that peptide sequence coverage increased from 10.3% (digestion time 10 min) to 89.1% (digestion time 30 min). μPPMER can efficiently digest proteins due to the microscopic confinement effect, showing its potential application in fast protein identification and protease immobilization. Applications of on-line digestion using μPPMER with human plasma and urinary proteome samples showed that the developed on-line method yielded equivalent or better performance in protein coverage and identified more membrane proteins than the in-solution method. This may be due to easy accommodation of hydrophobic membrane proteins within membrane pores. - Highlights: • A porous polymer membrane enzyme reactor was developed. • Breath figure method was used for the fabrication of porous polymer membrane. • The enzyme reactor was coupled to nLC-ESI-MS/MS for proteins on-line digestion.

Plant Oil-Derived Epoxy Polymers toward Sustainable Biobased Thermosets.

Science.gov (United States)

Wang, Zhongkai; Yuan, Liang; Ganewatta, Mitra S; Lamm, Meghan E; Rahman, Md Anisur; Wang, Jifu; Liu, Shengquan; Tang, Chuanbing

2017-06-01

Epoxy polymers (EPs) derived from soybean oil with varied chemical structures are synthesized. These polymers are then cured with anhydrides to yield soybean-oil-derived epoxy thermosets. The curing kinetic, thermal, and mechanical properties are well characterized. Due to the high epoxide functionality per epoxy polymer chain, these thermosets exhibit tensile strength over an order of magnitude higher than a control formulation with epoxidized soybean oil. More importantly, thermosetting materials ranging from soft elastomers to tough thermosets can be obtained simply by using different EPs and/or by controlling feed ratios of EPs to anhydrides. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Mechanical and thermal properties of polymer composite based on natural fibers: Moroccan hemp fibers/polypropylene

International Nuclear Information System (INIS)

Elkhaoulani, A.; Arrakhiz, F.Z.; Benmoussa, K.; Bouhfid, R.; Qaiss, A.

2013-01-01

Highlights: ► Moroccan hemp fibers are used as reinforcement in thermoplastic matrix. ► Moroccan hemp fiber was alkali treated to remove waxes and noncellulosic component. ► Fiber–matrix adhesion was assured by the use of a SEBS-g-MA as a compatibilizer. - Abstract: Moroccan hemp is a cellulosic fiber obtained from the north of Morocco. Their use as reinforcement in thermoplastic matrix composite requires a knowledge of their morphology and structure. In this paper the Moroccan hemp fiber was alkali treated to remove waxes and noncellulosic surface components. Fiber/matrix adhesion was assured by the use of a styrene-(ethylene-butene)-styrene three-block copolymer grafted with maleic anhydride (SEBS-g-MA) as a compatibilizer. Scanning electron microscopy (SEM), Fourier transforms infrared spectroscopy (FT-IR), Thermogravimetric analysis (TGA), tensile and torsional tests were carried out for hemp fibers polypropylene composite and the compatibilized composite at different fiber content. Thus, the binary composite PP/hemp fibers (Alk) and ternary system with maleic anhydride indicate clearly an improved adhesion of the fiber to the matrix as results of the good interaction at the interface. A gain of 50% on the Young’s modulus of PP/hemp 25 wt.% without coupling agent and 74% on the PP/hemp 20 wt.% composite with the coupling agent were found. Tensile strength curve shows a remarkable stabilization when the coupling agent was used

Hybrid composites

CSIR Research Space (South Africa)

Jacob John, Maya

2009-04-01

Full Text Available mixed short sisal/glass hybrid fibre reinforced low density polyethylene composites was investigated by Kalaprasad et al [25].Chemical surface modifications such as alkali, acetic anhydride, stearic acid, permanganate, maleic anhydride, silane...

A glassy carbon electrode modified with an amphiphilic, electroactive and photosensitive polymer and with multi-walled carbon nanotubes for simultaneous determination of dopamine and paracetamole

International Nuclear Information System (INIS)

Liu, Ren; Zeng, Xuebiao; Liu, Jingcheng; Luo, Jing; Zheng, Yuanyi; Liu, Xiaoya

2016-01-01

The article describes an electrochemical sensor for simultaneous determination of dopamine (DA) and paracetamole (PAT). It is based on the use of an electroactive polymer (referred to as BPVCM) to functionalize multi-walled carbon nanotubes. BPVCM is a branched amphiphilic photo-sensitive and electroactive polymer that was obtained by copolymerization of a vinyl benzyl carbazole, maleic acid anhydride, 4-vinyl benzylthiol and a vinylbenzyl oxycoumarin. BPVCM efficiently disperses MWCNT in aqueous solution. The electropolymerization of the carbazole moieties of the BPVCM enhances the current response. It also facilitates electron transfer in the MWCNT-BPVCM hybrid as evidenced by cyclic voltammetry and electrochemical impedance spectroscopy. A glassy carbon electrode modified with the nanocomposite displays outstanding electrocatalytic activity towards DA and PAT. DA can be determined, best at a working voltage of 0.2 V (vs. SCE), in the 5 to 1000 μM concentration range with a 2.3 μM detection limit. PAT can be determined in parallel, at a working voltage of 0.39 V (vs. SCE), in the same concentration range with a 3.5 μM detection limit. This analytical range of this method is wider than that of most alternative methods. (author)

Reactive compatibilization in polymer alloys, recyclates and composites

Energy Technology Data Exchange (ETDEWEB)

Czvikovszky, T.; Hargitai, H.; Racz, I.; Csukat, G

1999-05-02

The efficiency of all composite materials depends on the fiber-matrix interface and its ability to transfer stress from the matrix to the fiber. Radiation treatment is a possible way to bind together the main components of the composite. In our earlier work we applied acrylic oligomer-treated fibers irradiated with low energy electron beam to reinforce recycled polypropylene. In the present work the interaction between the matrix and fibers - PAN and glass fibers - was investigated by ESCA (Electron Spectroscopy for Chemical Analysis). On the other hand, the conventional way of compatibilization - the effect of using maleic anhydride grafted PP as a coupling agent - was examined in flax fiber-PP composites.

Dynamics study of free volume properties of SMA/SMMA blends by PAL method

International Nuclear Information System (INIS)

Jiang, Z.Y.; Jiang, X.Q.; Huang, Y.J.; Lin, J.; Li, S.M.; Li, S.Z.; Hsia, Y.F.

2006-01-01

Miscibility of poly(styrene-co-maleic anhydride) (containing 7 wt% maleic anhydride)/poly(styrene-co-methyl methacrylate) (containing 40 wt% styrene) blends were previously studied. It was obtained that SMA70 (containing 70 wt% of SMA in SMA/SMMA blends) is miscible in molecular level but SMA20 is not. In this paper, the two blends selected were used to investigate the temperature dependence of free volume parameters. It showed there are different deviations of free volume parameters in SMA20 and SMA70, and it was interesting that temperature dependence of ortho-positronium lifetime τ 3 of the SMA20 mixture exhibits two breaks in the range temperature from 90 deg. C to 120 deg. C, which revealed that the mixture has two glass transition ranges. Also, ortho-positronium lifetime τ 3 of the SMA20 mixture is nearly constant in the temperature range from 130 deg. C to 160 deg. C. These indicated that SMA20 blend is phase-separated in room temperature and become miscible above 130 deg. C, which may be due to steric hindrance effect of phenyl rings of SMMA and SMA. From the deviation of o-Ps lifetimes of SMA70, the single glass transition temperature of SMA70 blend was shown. Combining the previous study, it was further concluded that PAL method seems to be a powerful method to detect in situ phase behavior of immiscible polymer blends and glass transition of miscible polymer blends

Molecular tailoring of solid surfaces

Energy Technology Data Exchange (ETDEWEB)

Evenson, Simon Alan

1997-07-01

The overall performance of a material can be dramatically improved by tailoring its surface at the molecular level. The aim of this project was to develop a universal technique for attaching dendrimers (well-defined, nanoscale, functional polymers) and Jeffamines (high molecular weight polymer chains) to the surface of any shaped solid substrate. This desire for controlled functionalization is ultimately driven by the need to improve material compatibility in various biomedical applications. Atomic force microscopy (AFM) was used initially to study the packing and structure of Langmuir-Blodgett films on surfaces, and subsequently resulted in the first visualization of individual, spherically shaped, nanoscopic polyamidoamine dendrimers. The next goal was to develop a methodology for attaching such macromolecules to inert surfaces. Thin copolymer films were deposited onto solid substrates to produce materials with a fixed concentration of surface anhydride groups. Vapor-phase functionalization reactions were then carried out with trifluorinated amines to confirm the viability of this technique to bond molecules to surfaces. Finally, pulsed plasma polymerization of maleic anhydride took this approach one stage further, by forming well-adhered polymer films containing a predetermined concentration of reactive anhydride groups. Subsequent functionalization reactions led to the secure attachment of dendrimers and Jeffamines at any desired packing density. An alternative route to biocompatibilization used 1,2-ethanedithiol to yield thiolated surfaces containing very high polymeric sulfur : carbon ratios. (author)

Molecular tailoring of solid surfaces

International Nuclear Information System (INIS)

Evenson, Simon Alan

1997-01-01

The overall performance of a material can be dramatically improved by tailoring its surface at the molecular level. The aim of this project was to develop a universal technique for attaching dendrimers (well-defined, nanoscale, functional polymers) and Jeffamines (high molecular weight polymer chains) to the surface of any shaped solid substrate. This desire for controlled functionalization is ultimately driven by the need to improve material compatibility in various biomedical applications. Atomic force microscopy (AFM) was used initially to study the packing and structure of Langmuir-Blodgett films on surfaces, and subsequently resulted in the first visualization of individual, spherically shaped, nanoscopic polyamidoamine dendrimers. The next goal was to develop a methodology for attaching such macromolecules to inert surfaces. Thin copolymer films were deposited onto solid substrates to produce materials with a fixed concentration of surface anhydride groups. Vapor-phase functionalization reactions were then carried out with trifluorinated amines to confirm the viability of this technique to bond molecules to surfaces. Finally, pulsed plasma polymerization of maleic anhydride took this approach one stage further, by forming well-adhered polymer films containing a predetermined concentration of reactive anhydride groups. Subsequent functionalization reactions led to the secure attachment of dendrimers and Jeffamines at any desired packing density. An alternative route to biocompatibilization used 1,2-ethanedithiol to yield thiolated surfaces containing very high polymeric sulfur : carbon ratios. (author)

Cellulose-polyhydroxylated fatty acid ester-based bioplastics with tuning properties: Acylation via a mixed anhydride system.

Science.gov (United States)

Heredia-Guerrero, José A; Goldoni, Luca; Benítez, José J; Davis, Alexander; Ceseracciu, Luca; Cingolani, Roberto; Bayer, Ilker S; Heinze, Thomas; Koschella, Andreas; Heredia, Antonio; Athanassiou, Athanassia

2017-10-01

The synthesis of microcrystalline cellulose (MCC) and 9,10,16-hydroxyhexadecanoic (aleuritic) acid ester-based bioplastics was investigated through acylation in a mixed anhydride (trifluoroacetic acid (TFA)/trifluoroacetic acid anhydride (TFAA)), chloroform co-solvent system. The effects of chemical interactions and the molar ratio of aleuritic acid to the anhydroglucose unit (AGU) of cellulose were investigated. The degree of substitution (DS) of new polymers were characterized by two-dimensional solution-state NMR and ranged from 0.51 to 2.60. The chemical analysis by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) confirmed the presence of aleuritate groups in the structure induces the formation of new H-bond networks. The tensile analysis and the contact angle measurement confirmed the ductile behavior and the hydrophobicity of the prepared bioplastics. By increasing the aleuritate amounts, the glass transition temperature decreased and the solubility of bioplastic films in most common solvents was improved. Furthermore, this new polymer exhibits similar properties compared to commercial cellulose derivatives. Copyright © 2017 Elsevier Ltd. All rights reserved.

Blends of nitrile butadiene rubber/poly (vinyl chloride: The use of maleated anhydride castor oil based plasticizer

Directory of Open Access Journals (Sweden)

Indiah Ratna Dewi

2016-06-01

Full Text Available Recently, much attention has been focused on research to replace petroleum-based plasticizers, with biodegradable materials, such as biopolymer which offers competitive mechanical properties. In this study, castor oil was modified with maleic anhydride (MAH to produce bioplasticizer named maleated anhydride castor oil (MACO, and used in nitrile butadiene rubber (NBR/poly vinyl chloride (PVC blend. The effect of MACO on its cure characteristics and mechanical properties of NBR/PVC blend has been determined. The reactions were carried out at different castor oil (CO/xylene ratios, i.e. 1:0 and 1:1 by weight, and fixed CO/MAH ratio, 1:3 by mole. DOP, CO, and MACO were added into each NBR/PVC blend according to the formula. It was found that the viscosity and safe process level of NBR/PVC blend is similar from all plasticizer, however, MACO (1:0 showed the highest cure rate index (CRI. MACO-based plasticizer gave a higher value of the mechanical properties of the NBR/PVC blend as compared to DOP based plasticizer. MACO (1:1 based plasticizer showed a rather significance performance compared to another type of plasticizers both before and after aging. The value of hardness, elongation at break, tensile strength, and tear strength were 96 Shore A, 155.91 %, 19.15 MPa, and 74.47 MPa, respectively. From this result, NBR/PVC blends based on MACO plasticizer can potentially replace the DOP, and therefore, making the rubber blends eco-friendly.

Effect of Multiple Extrusions on the Impact Properties of Polypropylene/Clay Nanocomposites

DEFF Research Database (Denmark)

Klitkou, Rasmus; Jensen, Erik Appel; Christiansen, Jesper de Claville

2012-01-01

Polypropylene (PP)-based polymer nanocomposites containing organically modified montmorillonite (OMMT) with and without maleic anhydride grafted PP, were compounded by twin-screw extrusion. The extrusion process was repeated various numbers of times to increase the extruder residence time (TR) and......) increased monotonically with increased TR by 70% from least dispersed to best dispersed, which was still 20% below the level for neat PP. Both the fracture initiation energy and propagation energy increased with TR, but the primary effect on ri came from the fracture propagation energy, which delivered 80...

Procedure and composition for secondary recovery of petroleum

Energy Technology Data Exchange (ETDEWEB)

Sullivan, F F

1968-03-04

A copolymer of vinyl methyl ether and maleic anhydride in a brine (sodium bicarbonate, sodium chloride, calcium chloride) was proposed, for secondary oil recovery in the presence of clays. The ratio of copolymer to salts should be 20 : 1 to 1 : 1500. The ratio between the multivalent salts and sodium bicarbonate is 5 : 1 to 1 : 600. The concentration of salts of multivalent cations should be present in the range of 0.0025 to 0.25% by weight. Alkali metal halides comprise 0.1 to 1% of the polymer solution.

Effect of ionizing radiation on the properties of prepared plastic/starch blends and their applications as biodegradable materials

International Nuclear Information System (INIS)

Khalil, S.A.

2010-01-01

Blends based on different ratios of plasticised starch (PLST), low density poly-ethyleen (LDPE) were prepared by mixing in extrouder. The LDPE/PLST/POMA (poly-olefin maleic anhydride) and LDPE/PLST/TMPTA (tri-methylol propane tri-acrylate) were exposed to different doses of electron beam. The effect of mixing and E-Beam irradiation on the thermal, mechanical, water absorption, and structure morphology properties were investigated. The results showed that the addition of compatibilizers and E-Beam irradiation improve all the physical properties, which provides suitable material based on natural polymer for biodegradable plastic.

Modification of wheat starch with succinic acid/acetic anhydride and azelaic acid/acetic anhydride mixtures I. Thermophysical and pasting properties.

Science.gov (United States)

Subarić, Drago; Ačkar, Durđica; Babić, Jurislav; Sakač, Nikola; Jozinović, Antun

2014-10-01

The aim of this research was to investigate the influence of modification with succinic acid/acetic anhydride and azelaic acid/acetic anhydride mixtures on thermophysical and pasting properties of wheat starch. Starch was isolated from two wheat varieties and modified with mixtures of succinic acid and acetic anhydride, and azelaic acid and acetic anhydride in 4, 6 and 8 % (w/w). Thermophysical, pasting properties, swelling power, solubility and amylose content of modified starches were determined. The results showed that modifications with mixtures of afore mentioned dicarboxylic acids with acetic anhydride decreased gelatinisation and pasting temperatures. Gelatinisation enthalpy of Golubica starch increased, while of Srpanjka starch decreased by modifications. Retrogradation after 7 and 14 day-storage at 4 °C decreased after modifications of both starches. Maximum, hot and cold paste viscosity of both starches increased, while stability during shearing at high temperatures decreased. % setback of starches modified with azelaic acid/acetic anhydride mixture decreased. Swelling power and solubility of both starches increased by both modifications.

Multifunctional e-spun colloidal nanofiber structures from various dispersed blends of PVA/ODA-MMT with PVP/ODA-MMT, poly(VP-alt-MA and AgNPs incorporated polymer complexes as electro-active platforms

Directory of Open Access Journals (Sweden)

U. Bunyatova

2016-07-01

Full Text Available This work presented a new approach to fabricate polymer nanocomposites films with nanofiber structures from solution blends of poly(vinyl alcohol + octadecyl amine-montmorillonite (ODA-MMT (matrix with poly(N-vinylpyrrolidone + ODA-MMT (partner-1, poly(N-vinylpyrrolidone-alt-maleic anhydride ((poly(VP-alt-MA + (ODA-MMT (partner-2 and their silver (Ag-carrying polymer complexes by electrospinning. Chemical and physical structures, surface morphologies, thermal behaviors, electrical conductivity and thermal resistance parameters of nanofiber structures were investigated. Poly(VP-alt-MA was used both as a crosslinker and a donor of the hydrophilic groups such as ‒COOH and ‒NH–C=O amide from pyrrolidone ring. Reactive poly(VP-alt-MA, in situ generated Ag nanoparticles (AgNPs and original partner polymer had an significant effect on the morphology and diameter distribution of nanofibers. High and excellent conductive behaviors were observed for the homopolymer and copolymer of VP based fiber structures, respectively. Upon successive chemical cross-linking of the nanofiber structures by reactive partner copolymer, the conductivity of nanofiber films as electro-active platforms dramatically increased to 3.90·10–2 S·cm–1 at room temperature. Comparative analysis results also indicated that electrical properties strongly depended on the loaded reactive organoclay and in situ generated AgNPs.

Nanoparticle self-assembly in mixtures of phospholipids with styrene/maleic acid copolymers or fluorinated surfactants

Science.gov (United States)

Vargas, Carolyn; Arenas, Rodrigo Cuevas; Frotscher, Erik; Keller, Sandro

2015-12-01

Self-assembling nanostructures in aqueous mixtures of bilayer-forming lipids and micelle-forming surfactants are relevant to in vitro studies on biological and synthetic membranes and membrane proteins. Considerable efforts are currently underway to replace conventional detergents by milder alternatives such as styrene/maleic acid (SMA) copolymers and fluorinated surfactants. However, these compounds and their nanosized assemblies remain poorly understood as regards their interactions with lipid membranes, particularly, the thermodynamics of membrane partitioning and solubilisation. Using 19F and 31P nuclear magnetic resonance spectroscopy, static and dynamic light scattering, and isothermal titration calorimetry, we have systematically investigated the aggregational state of a zwitterionic bilayer-forming phospholipid upon exposure to an SMA polymer with a styrene/maleic acid ratio of 3 : 1 or to a fluorinated octyl phosphocholine derivative called F6OPC. The lipid interactions of SMA(3 : 1) and F6OPC can be thermodynamically conceptualised within the framework of a three-stage model that treats bilayer vesicles, discoidal or micellar nanostructures, and the aqueous solution as distinct pseudophases. The exceptional solubilising power of SMA(3 : 1) is reflected in very low membrane-saturating and solubilising polymer/lipid molar ratios of 0.10 and 0.15, respectively. Although F6OPC saturates bilayers at an even lower molar ratio of 0.031, this nondetergent does not solubilise lipids even at >1000-fold molar excess, thus highlighting fundamental differences between these two types of mild membrane-mimetic systems. We rationalise these findings in terms of a new classification of surfactants based on bilayer-to-micelle transfer free energies and discuss practical implications for membrane-protein research.Self-assembling nanostructures in aqueous mixtures of bilayer-forming lipids and micelle-forming surfactants are relevant to in vitro studies on biological and

Structure/property relationships in methacrylate/dimethacrylate polymers for dental applications

Science.gov (United States)

Mehlem, Jeremy John

as in their final state. Using these methods the size of the high and low cross-link density phase was examined and determined to be on the order of 50--150 nanometers. Model compounds based on phenylethyl methacrylate were formulated to determine how of nadic methyl anhydride and maleic anhydride incorporate into dimethacrylate resin systems.

Probing molecular interactions of poly(styrene-co-maleic acid) with lipid matrix models to interpret the therapeutic potential of the co-polymer.

Science.gov (United States)

Banerjee, Shubhadeep; Pal, Tapan K; Guha, Sujoy K

2012-03-01

To understand and maximize the therapeutic potential of poly(styrene-co-maleic acid) (SMA), a synthetic, pharmacologically-active co-polymer, its effect on conformation, phase behavior and stability of lipid matrix models of cell membranes were investigated. The modes of interaction between SMA and lipid molecules were also studied. While, attenuated total reflection-Fourier-transform infrared (ATR-FTIR) and static (31)P nuclear magnetic resonance (NMR) experiments detected SMA-induced conformational changes in the headgroup region, differential scanning calorimetry (DSC) studies revealed thermotropic phase behavior changes of the membranes. (1)H NMR results indicated weak immobilization of SMA within the bilayers. Molecular interpretation of the results indicated the role of hydrogen-bond formation and hydrophobic forces between SMA and zwitterionic phospholipid bilayers. The extent of membrane fluidization and generation of isotropic phases were affected by the surface charge of the liposomes, and hence suggested the role of electrostatic interactions between SMA and charged lipid headgroups. SMA was thus found to directly affect the structural integrity of model membranes. Copyright © 2011 Elsevier B.V. All rights reserved.

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry

NARCIS (Netherlands)

Polgar, Lorenzo Massimo; van Duin, Martin; Picchioni, Francesco

2016-01-01

A method for using Diels Alder thermo-reversible chemistry as cross-linking tool for rubber products is demonstrated. In this work, a commercial ethylene-propylene rubber, grafted with maleic anhydride, is thermo-reversibly cross-linked in two steps. The pending anhydride moieties are first modified

Use of Diels-Alder Chemistry for Thermoreversible Cross-Linking of Rubbers : The Next Step toward Recycling of Rubber Products?

NARCIS (Netherlands)

Polgar, L. M.; van Duin, M.; Broekhuis, A. A.; Picchioni, F.

2015-01-01

A proof of principle for the use of Diels-Alder chemistry as a thermoreversible cross-linking tool for rubber products is demonstrated. A commercial ethylene-propylene rubber grafted with maleic anhydride has been thermoreversibly cross-linked in two steps. The pending anhydride rings were first

The cellular responses and antibacterial activities of silver nanoparticles stabilized by different polymers

Science.gov (United States)

Lin, Jiang-Jen; Lin, Wen-Chun; Dong, Rui-Xuan; Hsu, Shan-hui

2012-02-01

Silver nanoparticles (AgNPs) are known for their excellent antibacterial activities. The possible toxicity, however, is a major concern for their applications. Three types of AgNPs were prepared in this study by chemical processes. Each was stabilized by a polymer surfactant, which was expected to reduce the exposure of cells to AgNPs and therefore their cytotoxicity. The polymer stabilizers included poly(oxyethylene)-segmented imide (POEM), poly(styrene-co-maleic anhydride)-grafting poly(oxyalkylene) (SMA) and poly(vinyl alcohol) (PVA). The cytotoxicity of these chemically produced AgNPs to mouse skin fibroblasts (L929), human hepatocarcinoma cells (HepG2), and mouse monocyte macrophages (J774A1) was compared to that of physically produced AgNPs and gold nanoparticles (AuNPs) as well as the standard reference material RM8011 AuNPs. Results showed that SMA-AgNPs were the least cytotoxic among all materials, but cytotoxicity was still observed at higher silver concentrations (>30 ppm). Macrophages demonstrated the inflammatory response with cell size increase and viability decrease upon exposure to 10 ppm of the chemically produced AgNPs. SMA-AgNPs did not induce hemolysis at a silver concentration below 1.5 ppm. Regarding the antibacterial activity, POEM-AgNPs and SMA-AgNPs at 1 ppm silver content showed 99.9% and 99.3% growth inhibition against E. coli, while PVA-AgNPs at the same silver concentration displayed 79.1% inhibition. Overall, SMA-AgNPs demonstrated better safety in vitro and greater antibacterial effects than POEM-AgNPs and PVA-AgNPs. This study suggested that polymer stabilizers may play an important role in determining the toxicity of AgNPs.

Synthesis of Functional Materials by Radiation

International Nuclear Information System (INIS)

Noh, Y. C.; Kang, P. H.; Choi, J. H.

2006-06-01

The radiation crosslinking, grafting, curing and degradation can be easily adjusted and is easily reproducible by controlling the radiation dose. These studies aim to develop new biomaterials such as wound healing, tissue engineering and antiadhesion barrier. The effect of thermal treatment and irradiation on the physico-chemical properties of ultra-high molecular weight polyethylene (UHMWPE) used in orthopedic implants was investigated. If a large amount of polymer radicals remain trapped after the irradiation of ultra-high molecular weight polyethylene (UHMWPE), the radicals may significantly alter the physical properties of UHMWPE during long shelf storage and implantation for a long time period. UHMWPE irradiated in the molten state had a higher crosslinking extent and a lower wear rate than one irradiated in the room temperature. The radiation grafting technology can develop membrane of fuel cell and Li secondary battery and heavy metal absorbents. Proton exchange membranes were prepared by γ-irradiation-induced grafting of styrene into fluorinated polymer films and subsequent sulfonation. Results of the present work suggest that radiation induced-graft polymerization can be used as alternative method to blending to prepare polymer electrolyte membranes for lithium battery applications. The polypropylene-based compatibilizers, polypropylene-g-maleic anhydride (PP-MAH), polypropylene-g-maleic anhydride/styrene (PP-St/MAH), and polypropylene-g-acrylic acid (PP-AA), were prepared by a high energy irradiation method. The compatibilizing effect of newly prepared graft copolymers on immiscible PP/Nylon6 blends has been studied by means of UTM, SEM, and DSC techniques. The results indicate that PP-MAH and PP-St/MAH are more effective compatibilizers for PP/Nylon6 blends than PP-AA showing more than 30 % increase in impact strength, and the compatibilizing effect on PP/Nylon6 blends depends on molecular structure of the compatibilizers and the composition of the

78 FR 4792 - Epoxy Polymer; Exemption From the Requirement of a Tolerance

Science.gov (United States)

2013-01-23

... ENVIRONMENTAL PROTECTION AGENCY 40 CFR Part 180 [EPA-HQ-OPP-2012-0615; FRL-9364-6] Epoxy Polymer... residues of polymers of one or more diglycidyl ethers of bisphenol A, resorcinol, glycerol... and 1,2,3,6-tetrahydrophthalic anhydride; also referred to as epoxy polymer, when used as an inert...

Kinetics of Maleic Acid and Aluminum Chloride Catalyzed Dehydration and Degradation of Glucose

Energy Technology Data Exchange (ETDEWEB)

Zhang, Ximing; Hewetson, Barron B.; Mosier, Nathan S.

2015-04-16

We report the positive effect of maleic acid, a dicarboxylic acid, on the selectivity of hexose dehydration to 5-hydroxymethyfurfural (HMF) and subsequent hydrolysis to levulinic and formic acids. We also describe the kinetic analysis of a Lewis acid (AlCl3) alone and in combination with HCl or maleic acid to catalyze the isomerization of glucose to fructose, dehydration of fructose to HMF, hydration of HMF to levulinic and formic acids, and degradation of these compounds to humins. The results show that AlCl3 significantly enhances the rate of glucose conversion to HMF and levulinic acid in the presence of both maleic acid and HCl. In addition, the degradation of HMF to humins, rather than levulinic and formic acids, is reduced by 50% in the presence of maleic acid and AlCl3 compared to HCl combined with AlCl3. The results suggest different reaction mechanisms for the dehydration of glucose and rehydration of HMF between maleic acid and HCl.

Pharmacokinetics of Maleic Acid as a Food Adulterant Determined by Microdialysis in Rat Blood and Kidney Cortex

Directory of Open Access Journals (Sweden)

Mei-Ling Hou

2016-03-01

Full Text Available Maleic acid has been shown to be used as a food adulterant in the production of modified starch by the Taiwan Food and Drug Administration. Due to the potential toxicity of maleic acid to the kidneys, this study aimed to develop an analytical method to investigate the pharmacokinetics of maleic acid in rat blood and kidney cortex. Multiple microdialysis probes were simultaneously inserted into the jugular vein and the kidney cortex for sampling after maleic acid administration (10 or 30 mg/kg, i.v., respectively. The pharmacokinetic results demonstrated that maleic acid produced a linear pharmacokinetic phenomenon within the doses of 10 and 30 mg/kg. The area under concentration versus time curve (AUC of the maleic acid in kidney cortex was 5-fold higher than that in the blood after maleic acid administration (10 and 30 mg/kg, i.v., respectively, indicating that greater accumulation of maleic acid occurred in the rat kidney.

Poly(methyl vinyl ether-alt-maleic acid)-functionalized porous silicon nanoparticles for enhanced stability and cellular internalization.

Science.gov (United States)

Shahbazi, Mohammad-Ali; Almeida, Patrick V; Mäkilä, Ermei; Correia, Alexandra; Ferreira, Mónica P A; Kaasalainen, Martti; Salonen, Jarno; Hirvonen, Jouni; Santos, Hélder A

2014-03-01

Currently, developing a stable nanocarrier with high cellular internalization and low toxicity is a key bottleneck in nanomedicine. Here, we have developed a successful method to covalently conjugate poly(methyl vinyl ether-co-maleic acid) (PMVE-MA) copolymer on the surface of (3-aminopropyl)triethoxysilane-functionalized thermally carbonized porous silicon nanoparticles (APSTCPSi NPs), forming a surface negatively charged nanovehicle with unique properties. This polymer conjugated NPs could modify surface smoothness, charge, and hydrophilicity of the developed NPs, leading to considerable improvement in the colloidal and plasma stabilities via enhanced suspensibility and charge repulsion. Furthermore, despite the surface negative charge of the polymer-conjugated NPs, the cellular internalization was increased in both MDA-MB-231 and MCF-7 breast cancer cells. These results provide a proof-of-concept evidence that such polymer-based PSi nanocomposite can be extensively used as a promising candidate for intracellular drug delivery. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Effect of wood filler treatment and EBAGMA compatibilizer on morphology and mechanical properties of low density polyethylene/olive husk flour composites

Directory of Open Access Journals (Sweden)

2007-07-01

Full Text Available This paper deals with plastic-wood composites based on low density polyethylene (LDPE and olive husk flour (OHF. The problem of incompatibility between the hydrophilic wood filler and the LDPE hydrophobic matrix was treated by two methods: a chemical modification of the olive husk flour with maleic anhydride to esterify the free hydroxyl groups of the wood components and the use of a compatibilizer agent, i.e. an ethylene-butyl acrylate-glycidyl methacrylate (EBAGMA terpolymer. The changes in the structure, the morphology, and the properties resulting from these treatments were followed by various techniques, especially FTIR spectroscopy, scanning electron microscopy (SEM, tensile measurements and water absorption. The experimental results indicated that both methods, i.e. the chemical treatment of the olive husk flour with maleic anhydride and the inclusion of EBAGMA terpolymer, improved the interactions between the two composite components and promoted better dispersion of the filler in the matrix. Moreover, ultimate tensile properties were also increased. However, the use of EBAGMA terpolymer as compatibilizer produced better enhancement of the properties of LDPE/OHF composites compared to those treated with maleic anhydride.

Structural studies of 4-aminoantipyrine derivatives

Science.gov (United States)

Cunha, Silvio; Oliveira, Shana M.; Rodrigues, Manoel T.; Bastos, Rodrigo M.; Ferrari, Jailton; de Oliveira, Cecília M. A.; Kato, Lucília; Napolitano, Hamilton B.; Vencato, Ivo; Lariucci, Carlito

2005-10-01

Reaction of 4-aminoantipyrine with acetylacetone, ethyl acetoacetate, benzoyl isothiocyanate, phenyl isothiocyanate, maleic anhydride and methoxymethylene Meldrum's acid afforded a series of new antipyrine derivatives. The antibacterial activity of the synthesized compounds against Micrococcus luteus ATCC 9341, Staphilococcus aureus ATCC 29737, and Escherichia coli ATCC 8739 was evaluated and the minimal inhibitory concentration determined. Modest activity was found only to the maleamic acid obtained from the reaction of 4-aminoantipyrine and maleic anhydride. 1H NMR investigation of this maleamic acid showed that it is slowly converted to the corresponding toxic maleimide. The structures of three derivatives were determined by X-ray diffraction analysis.

Preparation and characterization of poly(methyl methacrylate)-clay nanocomposites via melt intercalation: Effect of organoclay on thermal, mechanical and flammability properties

Energy Technology Data Exchange (ETDEWEB)

Unnikrishnan, Lakshmi; Mohanty, Smita [Laboratory for Advanced Research in Polymeric Materials (LARPM), Central Institute of Plastics Engineering and Technology, Bhubaneswar 751024 (India); Nayak, Sanjay K., E-mail: drsknayak@gmail.com [Laboratory for Advanced Research in Polymeric Materials (LARPM), Central Institute of Plastics Engineering and Technology, Bhubaneswar 751024 (India); Ali, Anwar [Laboratory for Advanced Research in Polymeric Materials (LARPM), Central Institute of Plastics Engineering and Technology, Bhubaneswar 751024 (India)

2011-05-15

Research highlights: {yields} The present work deals with preparation and characterization of poly(methyl methacrylate) nanocomposites via melt intercalation technique. {yields} The effect of various modified nanoclays on the properties of base matrix has been investigated. {yields} It was observed that compatibilization using maleic anhydride improved the performance characteristics of PMMA/layered silicate nanocomposites. - Abstract: The PMMA nanocomposites were prepared by melt processing method. The influence of organoclay loading on extent of intercalation, thermal, mechanical and flammability properties of poly(methyl methacrylate) (PMMA)-clay nanocomposites were studied. Three different organoclay modifiers with varying hydrophobicity (single tallow vs. ditallow) were investigated. The nanocomposites were characterized by using wide angle X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, differential scanning calorimetry (DSC), and tensile tests. The intercalation of polymer chain within the silicate galleries was confirmed by WAXD and TEM. Mechanical properties such as tensile modulus (E), tensile strength, percentage elongation at break and impact strength were determined for nanocomposites at various clay loadings. Overall thermal stability of nanocomposites increased by 16-17 deg. C. The enhancement in T{sub g} of nanocomposite is merely by 2-4 deg. C. The incorporation of maleic anhydride as compatibilizer further enhanced all the properties indicating improved interface between PMMA and clay. The flammability characteristics were studied by determining the rate of burning and LOI.

Preparation and characterization of poly(methyl methacrylate)-clay nanocomposites via melt intercalation: Effect of organoclay on thermal, mechanical and flammability properties

International Nuclear Information System (INIS)

Unnikrishnan, Lakshmi; Mohanty, Smita; Nayak, Sanjay K.; Ali, Anwar

2011-01-01

Research highlights: → The present work deals with preparation and characterization of poly(methyl methacrylate) nanocomposites via melt intercalation technique. → The effect of various modified nanoclays on the properties of base matrix has been investigated. → It was observed that compatibilization using maleic anhydride improved the performance characteristics of PMMA/layered silicate nanocomposites. - Abstract: The PMMA nanocomposites were prepared by melt processing method. The influence of organoclay loading on extent of intercalation, thermal, mechanical and flammability properties of poly(methyl methacrylate) (PMMA)-clay nanocomposites were studied. Three different organoclay modifiers with varying hydrophobicity (single tallow vs. ditallow) were investigated. The nanocomposites were characterized by using wide angle X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, differential scanning calorimetry (DSC), and tensile tests. The intercalation of polymer chain within the silicate galleries was confirmed by WAXD and TEM. Mechanical properties such as tensile modulus (E), tensile strength, percentage elongation at break and impact strength were determined for nanocomposites at various clay loadings. Overall thermal stability of nanocomposites increased by 16-17 deg. C. The enhancement in T g of nanocomposite is merely by 2-4 deg. C. The incorporation of maleic anhydride as compatibilizer further enhanced all the properties indicating improved interface between PMMA and clay. The flammability characteristics were studied by determining the rate of burning and LOI.

Effects of electric fields in polymerization on enthalpy of PMAA anhydridization

Energy Technology Data Exchange (ETDEWEB)

Chang Zhenqi; Liu Gang; Zhang Zhicheng

2004-02-19

PMAA (polymethacrylic acid) polymerized by {gamma}-irradiation in electric field forms six-membered cyclic anhydride during heating process and the enthalpy of PMAA anhydridization was determined by DSC. Why the endothermic peak of PMAA anhydridization in DSC curve between 200 and 300 deg. C appears is particularly explained by calculation. The relations between applied electric field and the enthalpy of PMAA anhydridization are studied. The results show that, with the increases of the intensity of electric field in polymerization, the enthalpy of PMAA forming anhydrides nonlinearly increase, which might be related to orientation of carboxylic acid groups of the PMAA in an electric field.

A study of the barrier properties of polyethylene coated with a nanocellulose/magnetite composite film

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Đorđević Nenad

2016-01-01

Full Text Available The morphological, thermal and barrier properties of low-density polyethylene/polycaprolactone-modified nanocellulose hybrid materials were investigated in this paper. Nanonocelulose/magnetite (NC-Fe3O4 nanocomposite and maleic acid functionalized NC/magnetite (NCMA-Fe3O4 nanocomposite were prepared and used as filler at various concentrations (5, 10 and 15 wt. % in polycaprolactone (PCL layer. PE was coated with PCL/NC/magnetite layer. The addition of the filler did not unfavorably affect the inherent properties of the polymer, especially its barrier properties. Oxygen permeation measurements show that the oxygen barrier properties of magnetite enriched PCL film were improved due to chemical activity of added material. The highest level of barrier capacity was observed for PE samples coated with PCL based composite with NCMA-Fe3O4 micro/-nanofiller, which implies the significant contribution of nanocellulose surface modification with maleic anhydride residue to improved barrier properties. [Projekat Ministarstva nauke Republike Srbije, br. III45019 i br. OI172013

Metal-ion retention properties of water-soluble amphiphilic block copolymer in double emulsion systems (w/o/w) stabilized by non-ionic surfactants.

Science.gov (United States)

Palencia, Manuel; Rivas, Bernabé L

2011-11-15

Metal-ion retention properties of water-soluble amphiphilic polymers in presence of double emulsion were studied by diafiltration. Double emulsion systems, water-in-oil-in-water, with a pH gradient between external and internal aqueous phases were prepared. A poly(styrene-co-maleic anhydride) (PSAM) solution at pH 6.0 was added to the external aqueous phase of double emulsion and by application of pressure a divalent metal-ion stream was continuously added. Metal-ions used were Cu(2+) and Cd(2+) at the same pH of polymer solution. According to our results, metal-ion retention is mainly the result of polymer-metal interaction. Interaction between PSMA and reverse emulsion globules is strongly controlled by amount of metal-ions added in the external aqueous phase. In addition, as metal-ion concentration was increased, a negative effect on polymer retention capacity and promotion of flocculation phenomena were produced. Copyright © 2011 Elsevier Inc. All rights reserved.

In vitro Degradation of Butanediamine-Grafted Poly(DL-Lactic acids)

Institute of Scientific and Technical Information of China (English)

无

2007-01-01

The degradation of butanediamine-grafted poly(DL-lactic acid) polymers (BDPLAs) in vitro together with PDLLA and maleic anhydride-grafted poly(DL-lactic acid) polymers (MPLAs) was investigated by observation of the changes of the pH value of incubation media, and weight loss ratio during degradation duration of 12 weeks. The results reveal that the acidity of PDLLA degradation products was weakened or neutralized by grafting butanediamine onto PDLLA. A uniform degradation of BDPLAs was observed in comparison with an acidity-induced auto-accelerating degradation featured by PDLLA and MPLAs. The biodegradation behaviors of BDPLAs can be adjusted by controlling the content of BDA. BDPLAs might be a new derivative of PDLLA-based biodegradable materials for medical applications without acidity-caused irritations and acidity-induced auto-accelerating degradation behavior as that of PDLLA.

Studies on the antifungal activities of the novel synthesized chelating co-polymer emulsion lattices and their silver complexes

Directory of Open Access Journals (Sweden)

Abd-El-Ghaffar M.A.

2008-01-01

Full Text Available The novel binary chelating co-polymers of butyl acrylate with itaconic and maleic acids were prepared by emulsion polymerization process. The chelating co-polymers of butyl acrylate-co-itaconic acid (BuA/IA and butyl acrylate-co-maleic acid (BuA/MA and their silver complexes were characterized and identified using IR spectroscopy and differential scanning calorimetry (DSC measurements. The biological activities of these compounds were studied against various types of fungal species. The dose and the rate of leached silver ions were controlled by the type of the co-polymers used and the solubility in the medium. The results provided laboratory support for the concept that the polymers containing chemically bound biocide are useful for controlling microbial growth. The silver uptake by strains of different fungal species was studied to determine their difference in behavior to the antifungal activities of these compounds. The uptake strategy was examined by transmission electron microscopy (TEM.

Evaluation of Scotchbond Multipurpose and maleic acid as alternative methods of bonding orthodontic brackets.

Science.gov (United States)

Olsen, M E; Bishara, S E; Damon, P; Jakobsen, J R

1997-05-01

Damage to the enamel surface during bonding and debonding of orthodontic brackets is a clinical concern. Alternative bonding methods that minimize enamel surface damage while maintaining a clinically useful bond strength is an aim of current research. The purpose of this study was to compare the effects on bond strength and bracket failure location of two adhesives (System 1+ and Scotchbond Multipurpose, 3M Dental Products Division) and two enamel conditioners (37% phosphoric acid and 10% maleic acid). Forty-eight freshly extracted human premolars were pumiced and divided into four groups of 12 teeth, and metal orthodontic brackets were attached to the enamel surface by one of four protocols: (1) System 1+ and phosphoric acid, (2) Scotchbond and phosphoric acid, (3) System 1+ and maleic acid, and (4) Scotchbond and maleic acid. After bracket attachment, the teeth were mounted in phenolic rings and stored in deionized water at 37 degrees C for 72 hours. A Zwick universal testing machine (Zwick GmbH & Co.) was used to determine shear bond strengths. The residual adhesive on the enamel surface was evaluated with the Adhesive Remnant Index. The analysis of variance was used to compare the four groups. Significance was predetermined at p adhesives on the enamel surfaces, revealed significant differences among the four groups (mean 2 = 0.005). A Duncan multiple range test revealed the difference occurred between the phosphoric acid and maleic acid groups, with maleic acid having bond failures at the enamel-adhesive interface. In conclusion, the use of Scotchbond Multipurpose and/or maleic acid does not significantly effect bond strength, however, the use of maleic acid resulted in an unfavorable bond failure location.

Compatibility of polyvinyl alcohol and poly(methyl vinyl ether-co-maleic acid) blends estimated by molecular dynamics

CSIR Research Space (South Africa)

Moolman, FS

2005-07-25

Full Text Available are not dissociated (ionized). At pH below pKa (negative logarithm of acid dissociation constant) of maleic acid (first and second dissociation constants at 25 8C are pKa1Z1.91 and pKa 2Z6.33, respectively [22]), ioniz- ation of the carboxylic acid groups in the PMVE...-MA. Decreasing pH also reduces absolute viscosities and broadens the optimum blend ratio peak. Fig. 2. Density of a selected number of runs (11?15) as a function of time. F.S. Moolman et al. / Polymer 46 (2005) 6192?6200 6195 The cohesive energy densities display...

Studies in reactive extrusion processing of biodegradable polymeric materials

Science.gov (United States)

Balakrishnan, Sunder

were comparable to linear low density Polyethylene (LDPE). Ecoflex-Thermoplastic Starch (TPS) graft co-polymers were continuously manufactured in melt with maleic acid catalyst using a twin-screw co-rotating extruder. The graft co-polymer was completely extractable in Dichloromethane and formed transparent films on solvent casting. Regular corn-starch was maleated in a twin-screw extruder using maleic anhydride or maleic acid, glycerol plasticizer and optional radical initiator. Confirmation of reactivity of maleic acid onto the starch backbone was confirmed by Fourier Transformed Infra Red (FTIR) Spectroscopy. (Abstract shortened by UMI.)

An efficient acetylation of dextran using in situ activated acetic anhydride with iodine

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MUHAMMAD A. HUSSAIN

2010-02-01

Full Text Available A facile, efficient, cost-effective and solvent-free acetylation method has been developed for the acetylation of dextran. Dextran acetates were successfully synthesized using different molar ratios of acetic anhydride in the presence of iodine as a catalyst without the use of any solvent. The reactions were realized at 50 °C for 3 h under stirring and nitrogen. This efficient method yielded highly pure and organosoluble dextran esters. The reaction appears highly effective for obtaining higher degrees of substitution (DS with great efficiency. Under solvent-free conditions, dextran triacetates were efficiently synthesized. It was also observed that the molar ratio can easily control the DS of pendant groups onto the polymer backbone. Hence, a range of products with varying DS were successfully designed, purified and characterized. Covalent attachment of the pendant groups onto the polymer backbone was verified by spectroscopic techniques. Thermogravimetric analysis indicated that the obtained dextran esters were thermally as stable as dextran. The DS of the pendant groups onto the polymer backbone was calculated using standard acid base titration after saponification. Furthermore, all products were thoroughly characterized by thermal analysis (TG and DTG, and FTIR and 1H-NMR spectroscopic analysis.

Poly(ester-anhydride):poly(beta-amino ester) micro- and nanospheres: DNA encapsulation and cellular transfection.

Science.gov (United States)

Pfeifer, Blaine A; Burdick, Jason A; Little, Steve R; Langer, Robert

2005-11-04

Poly(ester-anhydride) delivery devices allow flexibility regarding carrier dimensions (micro- versus nanospheres), degradation rate (anhydride versus ester hydrolysis), and surface labeling (through the anhydride functional unit), and were therefore tested for DNA encapsulation and transfection of a macrophage P388D1 cell line. Poly(l-lactic acid-co-sebacic anhydride) and poly(l-lactic acid-co-adipic anhydride) were synthesized through melt condensation, mixed with 25 wt.% poly(beta-amino ester), and formulated with plasmid DNA (encoding firefly luciferase) into micro- and nanospheres using a double emulsion/solvent evaporation technique. The micro- and nanospheres were then characterized (size, morphology, zeta potential, DNA release) and assayed for DNA encapsulation and cellular transfection over a range of poly(ester-anhydride) copolymer ratios. Poly(ester-anhydride):poly(beta-amino ester) composite microspheres (6-12 microm) and nanospheres (449-1031 nm), generated with copolymers containing between 0 and 25% total polyanhydride content, encapsulated plasmid DNA (>or=20% encapsulation efficiency). Within this polyanhydride range, poly(adipic anhydride) copolymers provided DNA encapsulation at an increased anhydride content (10%, microspheres; 10-25%, nanospheres) compared to poly(sebacic anhydride) copolymers (1%, microspheres and nanospheres) with cellular transfection correlating with the observed DNA encapsulation.

Journal of Chemical Sciences | Indian Academy of Sciences

Indian Academy of Sciences (India)

) andMn(II) complexes of poly(methyl vinyl ether-alt-maleic anhydride). Synthesis, characterization and thermodynamic parameters. Hidayet Mazi Ali Gulpinar. Volume 126 Issue 1 January 2014 pp 239-245 ...

Characteristic of Irradiation Result Film of Poly-Propylene-Co-Ethylene/Poly-ε-Caprolactone and Poly-Propylene Grafted Maleic Anhydrate Blend

International Nuclear Information System (INIS)

Nikham

2004-01-01

The effect of gamma rays irradiation to film of melt-blending polypropylene-co-ethylene (CPP) and poly-ε-caprolactone (PCL) with polypropylene grafted maleic anhydride (PP-g-MAH) blend as compatibilizer has been studied. The objective of the research is to prepare the biodegradable polyblend. The composition blend of CPP/PCL with 0, 10, 15, 20 wt % PP-g-MAH i.e. 100/0, 75/25, 50/50, 25/75 and 0/100 were irradiated by using gamma rays 60 Co with activity 420 kCi at doses; 0, 50, 100, 150, 200 kGy, at dose rate 8.2 kGy/hrs and temperature 90 o C. The elongation at break, tensile strength, gel fraction, enzymatic degradation and heat resistance were evaluated. The results showed that the compatibility of PP-g-MAH to reach good enough polyblend is 20 % weight. Elongation at break film of CPP/PCL 50/50 blend which irradiated at dose 200 kGy decreased, whereas the tensile strength increased. Gel fraction and heat resistance of the film irradiated increased. Enzyme of lipase AK can degraded either without irradiated or irradiated film. Thus quality of the polyblend can be called as biodegradable plastic material. (author)

Hydrolysis of Acetic Anhydride in a CSTR

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Veronica N. Coraci

2016-05-01

Full Text Available To find the optimal reactor volume and temperature for the hydrolysis of acetic anhydride at the lowest possible cost with a 90% conversion of acetic anhydride, a formula for the total cost of the reaction was created. Then, the first derivative was taken to find a value for the temperature. This value was then inputted into the second derivative of the equation to find the sign of the value which would indicate whether that point was a minima or maxima value. The minima value would then be the lowest total cost for the optimum reaction to take place.

Effects of fiber/matrix interactions on the interfacial deformation micromechanics of cellulose-fiber/polymer composites

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Tze, William Tai-Yin

The overall objective of this dissertation was to gain an understanding of the relationship between interfacial chemistry and the micromechanics of the cellulose-fiber/polymer composites. Regenerated cellulose (lyocell) fibers were treated with amine-, phenylamine-, phenyl-, and octadecyl-silanes, and also styrene-maleic anhydride copolymer. Inverse gas chromatography was conducted to evaluate the modified surfaces and to examine the adsorption behavior of ethylbenzene, a model compound for polystyrene, onto the fibers. Micro-composites were formed by depositing micro-droplets of polystyrene onto single fibers. The fiber was subjected to a tensile strain, and Raman spectroscopy was employed to determine the point-to-point variation of the strain- and stress-sensitive 895 cm-1 band of cellulose along the embedded region. Inverse gas chromatography studies reveal that the Ia-b values, calculated by matching the Lewis acid parameter ( KA) and basic parameter (KB) between polystyrene and different fibers, were closely correlated to the acid-base adsorption enthalpies of ethylbenzene onto the corresponding fibers. Hence, Ia-b was subsequently used as a convenient indicator for fiber/matrix acid-base interaction. The Raman micro-spectroscopic studies demonstrate that the interfacial tensile strain and stress are highest at the edge of the droplet, and these values decline from the edge region to the middle region of the embedment. The maximum of these local strains corresponds to a strain-control fracture of the matrix polymer. The minimum of the local tensile stress corresponds to the extent of fiber-to-matrix load transfer. The slope of the tensile stress profile allows for an estimation of the maximum interfacial shear stress, which is indicative of fiber/polymer (practical) adhesion. As such, a novel micro-Raman tensile technique was established for evaluating the ductile-fiber/brittle-polymer system in this study. The micro-Raman tensile technique provided maximum

An additive for a petroleum coke and water suspension

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Khiguti, K.; Igarasi, T.; Isimura, Y.; Kharaguti, S.; Tsudzina, T.

1983-03-04

The patent covers an additive for a petroleum coke and watersuspension which contains soap of an aliphatic acid (AM) and or a salt of a maleic acid copolymer (SMK). The aliphatic acid soap is a salt of an alkaline earth metal of C6 to C22 aliphatic acid, an ammonium salt or a salt of a lower amine. The maleic acid copolymer is a salt (sodium, NH4) of a lower amine of a maleic anhydride copolymer with a copolymerizing vinyl additive. Capric acid, lauric acid, palmatic acid, aleic and other acids may be used as the aliphatic acid, while methylamine, trimethylamine, diethanolamine, morpholine and so on may be used as the lower amine salt. Ethylene, vinylchloride, methyl(meta)acrylate and so on are used as the polymerizing vinyl compound. The molar ratio of the maleic anhydride to the polymerizing vinyl compound is in a range from 1 to 1 to 1 to 10 (preferably 1 to 1 to 1 to 3). The maleic acid copolymer has a mean molecular mass within 1,000 to 5,000. The additive with the optimal composition contains a solvent, a thickener, an anticorrosion substance, anticoagulants, surfacants (PAV) and so on. A highly concentrated suspension of oil coke and water with a 50 to 75 percent concentration of powder form petroleum coke may be produced using the patented additive. Such a suspension is characterized by low viscosity, high stability and forms no foam during processing.

Acetylated starch of Ofada rice as a sustained polymer in ...

African Journals Online (AJOL)

Objectives: To formulate and evaluate repaglinide microspheres using acetylated starch of the indigenous rice species Oryza glaberrima Steud (Ofada) as polymer. Materials and Methods: Ofada rice starch was acetylated with acetic anhydride in pyridine (DS 2.68) and characterized for morphology (Scanning electron ...

Trifluoromethanesulfonic Anhydride as a Low-Cost and Versatile Trifluoromethylation Reagent.

Science.gov (United States)

Ouyang, Yao; Xu, Xiu-Hua; Qing, Feng-Ling

2018-04-19

A large number of reagents have been developed for the synthesis of trifluoromethylated compounds. However, an ongoing challenge in trifluoromethylation reaction is the use of less expensive and practical trifluoromethyl sources. We report herein the unprecedented direct trifluoromethylation of (hetero)arenes using trifluoromethanesulfonic anhydride as a radical trifluoromethylation reagent by merging photoredox catalysis and pyridine activation. Furthermore, introduction of both the CF 3 and OTf groups of the trifluoromethanesulfonic anhydride into internal alkynes to access tetrasubstituted trifluoromethylated alkenes was achieved. Since trifluoromethanesulfonic anhydride is a low-cost and abundant chemical, this method provides a cost-efficient and practical route to trifluoromethylated compounds. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

The potential of bamboo in the design of polymer composites

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Patrícia Santos Delgado

2012-08-01

Full Text Available Bamboo is an alternative sustainable material for use in product design and has been incorporated into the concepts of eco-design. Here, we investigated the mechanical properties and morphologies of low density polyethylene (LDPE/bamboo flour (BF composites that were modified with polyethylene-graft-maleic anhydride (PE-g-MA and glycerol. Scanning electron microscopy (SEM and tensile tests of the composites demonstrated poor adhesion between the filler and matrix. Contact angle measurement showed that the surface of LDPE was modified by the presence of the load. The thermal stability of the composites was studied by measuring the oxidation induction time (OIT. Preliminary bacterial penetration tests were performed using culture inoculums of E. coli and S. aureus to investigate the natural antibacterial and bacteriostatic properties attributed to bamboo. Furthermore, bamboo may have interesting antioxidant activity with potential for use in food packaging applications.

Dimethylthioarsinic anhydride: A standard for arsenic speciation

International Nuclear Information System (INIS)

Fricke, Michael; Zeller, Matthias; Cullen, William; Witkowski, Mark; Creed, John

2007-01-01

Dimethylthioarsinic acid (DMTA V ) has recently been identified in biological, dietary and environmental matrices. The relevance of this compound to the toxicity of arsenic in humans is unknown and further exposure assessment and metabolic studies are difficult to conduct because of the unavailability of a well characterized standard. The synthesis of DMTA V was accomplished by the reaction of dimethylarsinic acid (DMA V ) with hydrogen sulfide. The initial reaction product produced is DMTA V but multiple products over the course of the reaction are also observed. Therefore, a chromatographic separation was developed to monitor the reaction progress via LC-ICP-MS. In this synthesis, conversion of DMA V to DMTA V was not taken to completion to avoid the production of side products. The product was isolated from the starting material by standard organic techniques. Single crystal diffraction demonstrated that solid DMTA V is present in the form of the oxygen-bridged dimethylthioarsinic anhydride. Dissolution of the anhydride in water produces the acid form of DMTA V and the aqueous phase DMTA V provided a characteristic molecular ion of m/z 155 by LC-ESI-MS. The synthesis and isolation of dimethylthioarsinic anhydride provides a stable crystalline standard suitable for identification, toxicological study and exposure assessment of dimethylthioarsinic acid

Effects of single and double bonds in linkers on colorimetric and fluorescent sensing properties of polyving akohol grafting rhodamine hydrazides.

Science.gov (United States)

Geng, Tong-Mou; Wang, Xie; Wang, Zhu-Qing; Chen, Tai-Jie; Zhu, Hai; Wang, Yu

2015-03-01

Two rhodamine derivatives, N-mono-maleic acid amide-N'-rhodamine B hydrazide (MRBH) and N-mono-succinic acid amide-N'-rhodamine 6G hydrazide (SR6GH), were synthesized by amidation with maleic anhydride (MAH), succinic anhydride (SAH) and rhodamine B hydrazide, rhodamine 6G hydrazide, which were identified by FTIR, (1)H NMR and elemental analysis. Two water-soluble fluorescent materials (PVA-MRBH and PVA-SR6GH) were prepared via esterification reaction with N-mono-maleic acyl chloride amide-N'-rhodamine B hydrazide (MRBHCl) or N-mono-maleic acyl chloride amide-N'-rhodamine 6G hydrazide (SR6GHCl) and poly(vinyl alcohol) (PVA) in DMSO solution. The sensing behaviors of PVA-MRBH and PVA-SR6GH were explored by recording the fluorescence spectra in completely aqueous solution. Upon the addition of Cu(2+) and Fe(3+) ions to the aqueous solution of PVA-MRBH, visual color change from rose pink to amaranth and orange for Cu(2+) and Fe(3+) ions, respectively, and fluorescence quenching were observed. Titration of Cu(2+), Fe(3+), Cr(3+) or Hg(2+) into the aqueous solution of PVA-SR6GH, although they induced fluorescence enhancement, only Fe(3+) made the color changing from colorless to yellow. Moreover, other metal ions did not induce obvious changes to color and the fluorescence spectra.

Synthesis and property characterization of cassava starch grafted poly(acrylamide-co-(maleic acid)) superabsorbent via γ-irradiation

International Nuclear Information System (INIS)

Kiatkamjornwong, Suda; Mongkolsawat, Kanlaya; Sonsuk, Manit

2004-01-01

Graft copolymerizations of acrylamide and maleic acid onto cassava starch by a simultaneous irradiation technique using γ-rays as a initiator were carried out. Various important parameters of total dose, dose rate, monomer-to-cassava starch ratio and maleic acid content were studied. Addition of 2% ww -1 diprotic acid of maleic acid into the reaction mixture yields a saponified starch graft copolymer with a water absorption in distilled water as high as 2256g g -1 of its dried weight. The water absorption of these saponified graft copolymers insaline and buffer solutions was also measured. The water absorption depends largely on the cationic type and concentration of these solutions in terms of ionic strength. This research explains a charge transfer mechanism for graft copolymerization of maleic acid and acrylamide onto cassava starch, and describes the influential parameters that affect grafting efficiency and water absorption. (author)

Nicotine-selective radiation-induced poly(acrylamide/maleic acid) hydrogels

International Nuclear Information System (INIS)

Saraydin, D.; Karadag, E.; Caldiran, Y.; Gueven, O.

2001-01-01

Nicotine-selective poly(acrylamide/maleic acid) (AAm/MA) hydrogels prepared by γ-irradiation were used in experiments on swelling, diffusion, and interactions of the pharmaceuticals nicotine, nicotinic acid, nicotinamide, and nikethamide. For AAm/MA hydrogel containing 60 mg maleic acid and irradiated at 5.2 kGy, the studies indicated that swelling increased in the following order; nicotine>nicotinamide>nikethamide>nicotinic acid>water. Diffusions of water and the pharmaceuticals within the hydrogels were found to be non-Fickian in character. AAm/MA hydrogel sorbed only nicotine and did not sorb nicotinamide, nikethamide and nicotinic acid in the binding experiments. S-type adsorption in Giles's classification system was observed. Some binding and thermodynamic parameters for AAm/MA hydrogel-nicotine system were calculated using the Scatchard method. The values of adsorption heat and free energy of this system were found to be negative whereas adsorption entropy was found to be positive. (author)

Chitosan: poly(N-vinylpyrrolidone-alt-itaconic anhydride) nanocapsules—a promising alternative for the lung cancer treatment

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Raţă, Delia Mihaela, E-mail: iureadeliamihaela@yahoo.com [„Apollonia” University of Iasi, Faculty of Medical Dentistry, „Academician Ioan Haulică” Research Institute (Romania); Chailan, Jean-François, E-mail: chailan@univ-tln.fr [University of Sud Toulon-Var, « Matériaux-Polymères-Interfaces-Environnement Marin (MAPIEM) Laboratory (France); Peptu, Cătălina Anişoara, E-mail: catipeptu@yahoo.co.uk [“Gheorghe Asachi” Technical University of Iasi, Department of Natural and Synthetic Polymers, Faculty of Chemical Engineering and Environmental Protection (Romania); Costuleanu, Marcel, E-mail: mcostuleanu@yahoo.com [University of Medicine and Pharmacy “Grigore T. Popa”- Iaşi, Department of General Pathology, Faculty of Dental Medicine (Romania); Popa, Marcel, E-mail: marpopa2001@yahoo.fr [“Gheorghe Asachi” Technical University of Iasi, Department of Natural and Synthetic Polymers, Faculty of Chemical Engineering and Environmental Protection (Romania)

2015-07-15

This study reports the preparation of novel polymeric nanocapsules based on a natural polymer, chitosan and a synthetic one, poly(N-vinylpyrrolidone-alt-itaconic anhydride) [(poly(NVPAI)] using an interfacial condensation technique. The infrared spectroscopy studies confirmed the crosslinking through the presence of amide bonds, formed between the two polymers chains. The diameter of nanocapsules was found in the range of 126–214 nm and it was determined by dynamic light scattering method. Morphological characterization demonstrated their nano size, the spherical shape of the nanocapsules and the formation of hollow particles. The nanocapsules presented good swelling capacity in aqueous solutions. 5-Fluorouracil (5-FU) loading and release capacity was studied, the processes being controlled by the drug diffusion through the polymeric membrane. The obtained results were encouraging, showing that 5-FU-loaded nanocapsules had 70 % higher apoptotic effect on A549 tumour cells than the drug in free state or mixed with the nanocapsules.

Chitosan: poly( N-vinylpyrrolidone- alt-itaconic anhydride) nanocapsules—a promising alternative for the lung cancer treatment

Science.gov (United States)

Raţă, Delia Mihaela; Chailan, Jean-François; Peptu, Cătălina Anişoara; Costuleanu, Marcel; Popa, Marcel

2015-07-01

This study reports the preparation of novel polymeric nanocapsules based on a natural polymer, chitosan and a synthetic one, poly( N-vinylpyrrolidone- alt-itaconic anhydride) [(poly(NVPAI)] using an interfacial condensation technique. The infrared spectroscopy studies confirmed the crosslinking through the presence of amide bonds, formed between the two polymers chains. The diameter of nanocapsules was found in the range of 126-214 nm and it was determined by dynamic light scattering method. Morphological characterization demonstrated their nano size, the spherical shape of the nanocapsules and the formation of hollow particles. The nanocapsules presented good swelling capacity in aqueous solutions. 5-Fluorouracil (5-FU) loading and release capacity was studied, the processes being controlled by the drug diffusion through the polymeric membrane. The obtained results were encouraging, showing that 5-FU-loaded nanocapsules had 70 % higher apoptotic effect on A549 tumour cells than the drug in free state or mixed with the nanocapsules.

Chitosan: poly(N-vinylpyrrolidone-alt-itaconic anhydride) nanocapsules—a promising alternative for the lung cancer treatment

International Nuclear Information System (INIS)

Raţă, Delia Mihaela; Chailan, Jean-François; Peptu, Cătălina Anişoara; Costuleanu, Marcel; Popa, Marcel

2015-01-01

This study reports the preparation of novel polymeric nanocapsules based on a natural polymer, chitosan and a synthetic one, poly(N-vinylpyrrolidone-alt-itaconic anhydride) [(poly(NVPAI)] using an interfacial condensation technique. The infrared spectroscopy studies confirmed the crosslinking through the presence of amide bonds, formed between the two polymers chains. The diameter of nanocapsules was found in the range of 126–214 nm and it was determined by dynamic light scattering method. Morphological characterization demonstrated their nano size, the spherical shape of the nanocapsules and the formation of hollow particles. The nanocapsules presented good swelling capacity in aqueous solutions. 5-Fluorouracil (5-FU) loading and release capacity was studied, the processes being controlled by the drug diffusion through the polymeric membrane. The obtained results were encouraging, showing that 5-FU-loaded nanocapsules had 70 % higher apoptotic effect on A549 tumour cells than the drug in free state or mixed with the nanocapsules

Polyisobutenylsuccinimides as detergents and dispersants in fuel: infrared spectroscopy application

Energy Technology Data Exchange (ETDEWEB)

Aleman-Vazquez, L.O.; Villagomez-Ibarra, J.R. [Instituto Mexicano del Petrole, San Bartolo Atepehuacan (Mexico). Gerencia de Productos Quimicos

2001-05-01

Polyalkenylsuccinimides were synthesized and their dispersancy properties evaluated in an internal combustion engine. The synthesis is based on the reaction of polyisobutene with maleic anhydride as the first step. The polyisobutenylsuccinic anhydride obtained reacts with primary amines in the last step to give polyalkenylsuccinimides. The results of the evaluations showed that some polyisobutenylsuccinimides reduce the deposit formation in the intake system with good efficiency. Infrared spectra of the prepared compounds allowed their identification. 16 refs., 2 tabs.

Properties of SBS and sisal fiber composites: ecological material for shoe manufacturing

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José Carlos Krause de Verney

2008-12-01

Full Text Available The worldwide trend toward using cheap, atoxic and durable materials from renewable resources contributes to sustainable development. Thus, the investigation of the potential use of vegetal fibers as reinforcing agent in polymeric composites has gained new significance. Sisal fiber has emerged as a reinforcing material for polymers used in automobile, footwear and civil industries. In this work, properties such as hardness, tensile strength and tear strength of polymer composites composed by block copolymer styrene-butadiene-styrene (SBS and 5, 10 and 20% by weight of sisal fiber were evaluated. The influence of conventional polymer processing techniques such as single-screw and double-screw extrusion, as well as the addition of coupling agent on the composite mechanical performance was investigated. Also, the morphology and thermal stability of the composites were analyzed. The addition of 2 wt. (% maleic anhydride as coupling agent between sisal fiber and SBS has improved the composite mechanical performance and the processing in a double-screw extruder has favored the sisal fiber distribution in the SBS matrix.

Bridging adhesion and barrier properties with functional dispersions : towards waterborne anti-corrosion coatings

NARCIS (Netherlands)

Soer, W.J.

2008-01-01

The successful preparation of waterborne anti-corrosion coatings based on maleic anhydride containing copolymers is described in this thesis. To obtain good anticorrosion coatings, three different properties should be present in a coating system; they should display good mechanical properties, good

SHORT COMMUNICATION SOLVENT FREE PREPARATION OF N ...

African Journals Online (AJOL)

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KEYWORDS: Solvent free, Maleanilic acids, Maleic anhydride, Aniline derivatives ... associated with the carboxylic group between 3275-2877 cm-1, the weak –NH .... Chemical shifts (σ/ppm) relative to TMS*. O-H N-H Ha. Hb. Hc. Hd. He. Hf.

Facile fabrication of HDPE-g-MA/nanodiamond nanocomposites via one-step reactive blending.

Science.gov (United States)

Song, Ping'an; Yu, Youming; Wu, Qiang; Fu, Shenyuan

2012-06-29

In this letter, nanocomposites based on maleic anhydride grafted high density polyethylene (HDPE-g-MA) and amine-functionalized nanodiamond (ND) were fabricated via one-step reactive melt-blending, generating a homogeneous dispersion of ND, as evidenced by transmission electron microscope observations. Thermal analysis results suggest that addition of ND does not affect significantly thermal stability of polymer matrix in nitrogen. However, it was interestingly found that incorporating pure ND decreases the thermal oxidation degradation stability temperature, but blending amino-functionalized ND via reactive processing significantly enhances it of HDPE in air condition. Most importantly, cone tests revealed that both ND additives and reactive blending greatly reduce the heat release rate of HDPE. The results suggest that ND has a potential application as flame retardant alternative for polymers. Tensile results show that adding ND considerably enhances Young's modulus, and reactive blending leads to further improvement in Young's modulus while hardly reducing the elongation at break of HDPE.

The Effects of Coupling Agents on the Mechanical and Thermal Properties of Eucalyptus Flour/HDPE Composite

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Metanawin Siripan

2015-01-01

Full Text Available The aim of this research was to study the effects of the coupling agents, FusabondTM E-528 (polyethylene-grafted maleic anhydride; PE-g-MA, MA and Amino Silane (Si, on the thermal properties, and mechanical properties of Eucalyptus flour-HDPE composite. Variation of the Eucalyptus flour contents in the HDPE resulted in properties of the composite. With increasing in the contents of Eucalyptus flour in polymer matrix, the mechanical properties of the HDPE composite decreased in EU-MA series samples while they were gradually decreased in EU-Si series samples. SEM micrographs showed the fracture surface of the HDPE/Eucalyptus composite at different ratios of Eucalyptus flour. SEM micrograpgh exhibited the dispersion of EU flour in polymer matrix. The samples of both coupling agents showed an increase in interfacial adhesion, observed for the considerable decreased of gaps between the matrix and the dispersed phase. However, the EU-MA sample appeared to be more uniformly than the EU-Si sample.

Dimethylthioarsinic anhydride: A standard for arsenic speciation

Energy Technology Data Exchange (ETDEWEB)

Fricke, Michael [United States Environmental Protection Agency, National Exposure Research Laboratory, Microbiological and Chemical Exposure Assessment Research Division, 26 W. Martin Luther King Drive, Cincinnati, OH 45268 (United States); Zeller, Matthias [STaRBURSTT-Cyberdiffraction Consortium, Department of Chemistry, Youngstown State University, One University Plaza, Youngstown, OH 44555-3663 (United States); Cullen, William [Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, BC, V6T 1Z1 (Canada); Witkowski, Mark [Food and Drug Administration, Forensic Chemistry Center, Vibrational Spectroscopy Laboratory, 6751 Steger Drive, Cincinnati, OH 45237 (United States); Creed, John [United States Environmental Protection Agency, National Exposure Research Laboratory, Microbiological and Chemical Exposure Assessment Research Division, 26 W. Martin Luther King Drive, Cincinnati, OH 45268 (United States)]. E-mail: creed.jack@epa.gov

2007-01-30

Dimethylthioarsinic acid (DMTA{sup V}) has recently been identified in biological, dietary and environmental matrices. The relevance of this compound to the toxicity of arsenic in humans is unknown and further exposure assessment and metabolic studies are difficult to conduct because of the unavailability of a well characterized standard. The synthesis of DMTA{sup V} was accomplished by the reaction of dimethylarsinic acid (DMA{sup V}) with hydrogen sulfide. The initial reaction product produced is DMTA{sup V} but multiple products over the course of the reaction are also observed. Therefore, a chromatographic separation was developed to monitor the reaction progress via LC-ICP-MS. In this synthesis, conversion of DMA{sup V} to DMTA{sup V} was not taken to completion to avoid the production of side products. The product was isolated from the starting material by standard organic techniques. Single crystal diffraction demonstrated that solid DMTA{sup V} is present in the form of the oxygen-bridged dimethylthioarsinic anhydride. Dissolution of the anhydride in water produces the acid form of DMTA{sup V} and the aqueous phase DMTA{sup V} provided a characteristic molecular ion of m/z 155 by LC-ESI-MS. The synthesis and isolation of dimethylthioarsinic anhydride provides a stable crystalline standard suitable for identification, toxicological study and exposure assessment of dimethylthioarsinic acid.

Maleic acid treatment of biologically detoxified corn stover liquor.

Science.gov (United States)

Kim, Daehwan; Ximenes, Eduardo A; Nichols, Nancy N; Cao, Guangli; Frazer, Sarah E; Ladisch, Michael R

2016-09-01

Elimination of microbial and enzyme inhibitors from pretreated lignocellulose is critical for effective cellulose conversion and yeast fermentation of liquid hot water (LHW) pretreated corn stover. In this study, xylan oligomers were hydrolyzed using either maleic acid or hemicellulases, and other soluble inhibitors were eliminated by biological detoxification. Corn stover at 20% (w/v) solids was LHW pretreated LHW (severity factor: 4.3). The 20% solids (w/v) pretreated corn stover derived liquor was recovered and biologically detoxified using the fungus Coniochaeta ligniaria NRRL30616. After maleic acid treatment, and using 5 filter paper units of cellulase/g glucan (8.3mg protein/g glucan), 73% higher cellulose conversion from corn stover was obtained for biodetoxified samples compared to undetoxified samples. This corresponded to 87% cellulose to glucose conversion. Ethanol production by yeast of pretreated corn stover solids hydrolysate was 1.4 times higher than undetoxified samples, with a reduction of 3h in the fermentation lag phase. Copyright © 2016 Elsevier Ltd. All rights reserved.

Solution blow spun nanocomposites of poly(lactic acid)/cellulose nanocrystals from Eucalyptus kraft pulp

Science.gov (United States)

Cellulose nanocrystals (CNCs) were extracted from Eucalyptus kraft pulp by sulfuric acid hydrolysis, and esterified with maleic anhydride (CNCMA). The incorporation of sulfate ester groups on the cellulose surface resulted in higher stability of the nanoparticles in aqueous suspensions and lower the...

76 FR 76259 - National Emissions Standards for Hazardous Air Pollutants: Primary Aluminum Reduction Plants

Science.gov (United States)

2011-12-06

... Emissions From Maleic Anhydride Plants, Ethylbenzene/Styrene Plants, Benzene Storage Vessels, Benzene...). The rule is applicable to facilities with affected sources associated with the production of aluminum... are subject to the requirements of this NESHAP: 14 primary aluminum production plants and one carbon...

Synthesis and Characterization of Some New Thermal Stable Polymers - Polymerization of N-[4-N´ -(Benzylamino-carbonylphenyl]maleimide

Directory of Open Access Journals (Sweden)

B. L. Hiran

2007-01-01

Full Text Available This article describes the synthesis and characterization of homopolymer (H-BCPM of N-[4-N'-(benzylamino-carbonyl phenyl] maleimide (N-BACPMI and copolymer (C-BCPM of N-BACPMI with n-butyl acrylate (BA. The new monomer was synthesized from p-aminobenzoic acid, maleic anhydride and benzylamine. The homopolymerization of N-BACPMI is initiated by free radical using AIBN in THF solvent at 65°C. Radical copolymerization of N-BACPMI with BA, initiated by AIBN, was performed in THF solvent using equimolar amount. Effect of the different free radical initiator AIBN, BPO and solvents p-Dioxane, THF, DMF and DMSO was studied. Homopolymer and Copolymer were characterized by intrinsic viscosity, solubility test, FT-IR, 1H-NMR spectral analysis and elemental analysis. Thermal behaviour was studied by Thermo gravimetric analysis.

Tailoring the morphology and properties of poly(lactic acid)/poly(ethylene-co-vinyl acetate)/starch blends via reactive compatibilization

NARCIS (Netherlands)

Ma, P.; Hristova - Bogaerds, D.G.; Schmit, P.; Goossens, J.G.P.; Lemstra, P.J.

2012-01-01

Poly(lactic acid)/poly(ethylene-co-vinyl acetate)/starch (PLA/EVA/starch) ternary blends were prepared by multi-step melt processing (reactive extrusion) in the presence of maleic anhydride (MA), benzoyl peroxide and glycerol. The effects of MA and glycerol concentration on the morphology and

Synthesis and characterization of acrylated Parkia biglobosa ...

African Journals Online (AJOL)

The results revealed that acid functional acrylic copolymers containing maleic anhydride as a functional co-monomer can successfully be used to modify alkyd resins yielding acrylated resins with better drying, flexibility, scratch hardness, impact resistance and chemical resistance properties. However there exist optimum ...

In situ Raman spectroscopy studies of bulk and surface metal

NARCIS (Netherlands)

Weckhuysen, B.M.; Wachs, I.E.; Jehng, J.M.; Deo, G.; Guliants, V.V.; Benziger, J.B.

1996-01-01

Bulk V-P-O and model supported vanadia catalysts were investigated with in situ Raman spectroscopy during n-butane oxidation to maleic anhydride in order to determine the fundamental molecular structure-reactivity/selectivity insights that can be obtained from such experiments. The in situ Raman

MECHANICAL PROPERTIES AND WATER ABSORPTION OF KENAF POWDER FILLED RECYCLED HIGH DENSITY POLYETHYLENE/NATURAL RUBBER BIOCOMPOSITES USING MAPE AS A COMPATIBILIZER

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Azura A. Rashid

2011-06-01

Full Text Available The performance of kenaf powder (KP filled recycled high density polyethylene (rHDPE /natural rubber (NR blends with and without a compatibilizer, maleic anhydride grafted polyethylene (MAPE, were investigated. The composites with different filler loading (0 to 40 phr were prepared with a Haake internal mixer. Increasing the KP loading in rHDPE/NR/KP biocomposites reduced the tensile strength and the elongation at break but increased the stabilization torque and the tensile modulus. The addition of MAPE as a compatibilizer increased the tensile strength, elongation at break, and modulus of the composites. This might be attributed to the enhanced adhesion between the filler and polymer matrix, as evidenced from the morphology, using scanning electron microscopy. The incorporation of compatibilizer also reduced the water absorption of the composites.

Polypropylene reinforced with organophilic clay and brazilian nut fibers; Polipropileno reforcado com argila verde lodo e fibra da castanha-do-brasil

Energy Technology Data Exchange (ETDEWEB)

Rocha-Gomes, L.V.; Mondelo-Garcia, F.J.; Vaccioli, K.; Valera, S.T.; Silva-Valenzuela, M.G.; Valenzuela-Diaz, F.R., E-mail: leila@ifes.edu.br [Universidade de Sao Paulo (LPSS/PMT/EP/USP), SP (Brazil). Dept. de Engenharia Metalurgica e de Materiais. Lab. de Materiais Nao-Metalicos

2014-07-01

Polymer nanocomposites have been shown to possess better properties when compared with traditional composites. This study aims to investigate the effects of the addition of organophilic clay and Brazilian nut fiber on the polypropylene (PP). First, 5%, 10% and 20% PP/compatibilizer maleic anhydride (PP-g-MA) by weight was added to Pure PP, respectively. From the results, 5% PP-g-MA was defined for preparing the nanocomposites. Samples were prepared containing 5% PP / PP-g-MA reinforced with 5% organophilic Brazilian smectite clay and 5%, 10% and 15% Brazilian nut fiber. Specimens were tested for tensile strength and impact. The materials were characterized by laser diffraction particle size and X-ray diffraction, and the nanocomposites, by mechanical strength and impact. The best result was obtained by inserting 15% fiber. (author)

Polypropylene reinforced with organophilic clay and brazilian nut fibers

International Nuclear Information System (INIS)

Rocha-Gomes, L.V.; Mondelo-Garcia, F.J.; Vaccioli, K.; Valera, S.T.; Silva-Valenzuela, M.G.; Valenzuela-Diaz, F.R.

2014-01-01

Polymer nanocomposites have been shown to possess better properties when compared with traditional composites. This study aims to investigate the effects of the addition of organophilic clay and Brazilian nut fiber on the polypropylene (PP). First, 5%, 10% and 20% PP/compatibilizer maleic anhydride (PP-g-MA) by weight was added to Pure PP, respectively. From the results, 5% PP-g-MA was defined for preparing the nanocomposites. Samples were prepared containing 5% PP / PP-g-MA reinforced with 5% organophilic Brazilian smectite clay and 5%, 10% and 15% Brazilian nut fiber. Specimens were tested for tensile strength and impact. The materials were characterized by laser diffraction particle size and X-ray diffraction, and the nanocomposites, by mechanical strength and impact. The best result was obtained by inserting 15% fiber. (author)

Safe design and operation of fluidized-bed reactors: Choice between reactor models

NARCIS (Netherlands)

Westerink, E.J.; Westerterp, K.R.

1990-01-01

For three different catalytic fluidized bed reactor models, two models presented by Werther and a model presented by van Deemter, the region of safe and unique operation for a chosen reaction system was investigated. Three reaction systems were used: the oxidation of benzene to maleic anhydride, the

Switchgrass (Panicum virgatum L.) as a reinforcing fibre in polypropylene composites

NARCIS (Netherlands)

Oever, van den M.J.A.; Elbersen, H.W.; Keijsers, E.R.P.; Gosselink, R.J.A.; Klerk-Engels, de B.

2003-01-01

In this study the switchgrass (Panicum virgatum L.), a biomass crop being developed in North America and Europe, was tested as a stiffening and reinforcing agent in polypropylene (PP) composites with and without maleic anhydride grafted PP (MAPP) as a compatibiliser and to evaluate the effect of

Surface Polymerisation Methods for Optimised Adhesion

DEFF Research Database (Denmark)

Drews, Joanna Maria

Arbejdet har fokuseret på muligheder for at forstærke kompositmaterialer til højteknologiske anvendelser fx til vindmøllevinger. Forskningen har derfor været centreret om plasma polymerisation af henholdsvis maleic anhydrid (MAH) og 1,2-methylenedioxybenzen til tynde film på modelkulstofsubstrate...

The cell-type specific uptake of polymer-coated or micelle-embedded QDs and SPIOs does not provoke an acute pro-inflammatory response in the liver

Directory of Open Access Journals (Sweden)

Markus Heine

2014-09-01

Full Text Available Semiconductor quantum dots (QD and superparamagnetic iron oxide nanocrystals (SPIO have exceptional physical properties that are well suited for biomedical applications in vitro and in vivo. For future applications, the direct injection of nanocrystals for imaging and therapy represents an important entry route into the human body. Therefore, it is crucial to investigate biological responses of the body to nanocrystals to avoid harmful side effects. In recent years, we established a system to embed nanocrystals with a hydrophobic oleic acid shell either by lipid micelles or by the amphiphilic polymer poly(maleic anhydride-alt-1-octadecene (PMAOD. The goal of the current study is to investigate the uptake processes as well as pro-inflammatory responses in the liver after the injection of these encapsulated nanocrystals. By immunofluorescence and electron microscopy studies using wild type mice, we show that 30 min after injection polymer-coated nanocrystals are primarily taken up by liver sinusoidal endothelial cells. In contrast, by using wild type, Ldlr-/- as well as Apoe-/- mice we show that nanocrystals embedded within lipid micelles are internalized by Kupffer cells and, in a process that is dependent on the LDL receptor and apolipoprotein E, by hepatocytes. Gene expression analysis of pro-inflammatory markers such as tumor necrosis factor alpha (TNFα or chemokine (C-X-C motif ligand 10 (Cxcl10 indicated that 48 h after injection internalized nanocrystals did not provoke pro-inflammatory pathways. In conclusion, internalized nanocrystals at least in mouse liver cells, namely endothelial cells, Kupffer cells and hepatocytes are at least not acutely associated with potential adverse side effects, underlining their potential for biomedical applications.

Study of the dielectric properties of barium titanate-polymer composites

International Nuclear Information System (INIS)

Pant, H.C.; Patra, M.K.; Verma, Aditya; Vadera, S.R.; Kumar, N.

2006-01-01

A comparative study of complex dielectric properties has been carried out at the X-band of microwave frequencies of composites of barium titanate (BaTiO 3 ) with two different polymer matrices: insulating polyaniline (PANI) powder (emeraldine base) and maleic resin. From these studies, it is observed that the composites of BaTiO 3 with maleic resin show normal composite behavior and the dielectric constant follows the asymmetric Bruggeman model. In contrast, the composites of BaTiO 3 with PANI show an unusual behavior wherein even at a low concentration of PANI (5 wt.%) there is a drastic reduction in the dielectric constant of BaTiO 3 . This behavior of the dielectric constant is explained on the basis of coating of BaTiO 3 particles by PANI which in turn is attributed to the highly surface adsorbing character. The materials have also been characterized using Fourier transform infrared spectroscopy, powder X-ray diffraction, scanning electron microscopy and optical microscopy studies

Influence of the composition of hydroxypropyl cellulose/maleic acid-alt-styrene copolymer blends on their properties as matrix for drug release

Directory of Open Access Journals (Sweden)

2009-05-01

Full Text Available Poly(carboxylic acid-polysaccharide compositions have been found suitable for obtaining drug formulations with controlled release, most formulations being therapeutically efficacious, stable, and non-irritant. The influence of the characteristics of the aqueous solutions from which the polymer matrix is prepared (i.e. the total concentration of polymer in solutions and the mixing ratio between the partners, hydroxypropyl cellulose, HPC and maleic acid-alternating-styrene copolymer, MAc-alt-S on the kinetics of some drugs release in acidic environment (pH = 2 has been followed by ‘in vitro’ dissolution tests. It has been established that the kinetics of procaine hydrochloride release from HPC/MAc-alt-S matrix depends on its composition; the diffusion exponent, n is close to 0.5 for matrices where one of the components is in large excess and n~0.02 for middle composition range. The lower value of diffusion exponent for middle composition range could be caused by the so called ‘burst effect’, therefore the kinetic evaluation is difficult.

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

... glass slides coated with polyvinyl alcohol (PVA) crosslinked with maleic anhydride (MA). FTIR and XRD studies of the coated film were also done. AFM studies further helped in the morphological study of the film deposited. Finally, conductivity and ammonia gas-sensing property of the polyaniline film were also studied.

Synthesis and 1,3-Dipolar Cycloaddition Reactions of Chiral Maleimides

Directory of Open Access Journals (Sweden)

Lubor Fisera

1997-02-01

Full Text Available New routes to the synthesis of various novel chiral maleimides are described. The oxabicyclic anhydride 2 readily available exo-Diels-Alder adduct of furan and maleic anhydride was used as a vehicle, which in turn reacted with hydrochlorides of amino acids 3a-f in the presence of Et3N with release of furan to give the requisite novel chiral imides 4a-f in good to moderate yields. The stereoselectivity of 1,3-dipolar cycloaddition of nitrile oxides with prepared chiral imides 4a-f is investigated.

Evaluation of mechanical properties and durability performance of HDPE-wood composites

Energy Technology Data Exchange (ETDEWEB)

Tazi, M.; Erchiqui, F. [Engineering department, Université de Quebec en Abitibi-Témiscamingue (Canada); Kaddami, H. [Université Caddi Ayad Marrakech, Laboratoire ’LCO2MC’, B.P. 549, Marrakech 40000, Maroc (Morocco); Bouazara, M. [Mechanical department, Université de Québec à Chicoutimi Canada (Canada); Poaty, B. [Technology Center of industrial residuals, QC Canada (Canada)

2015-05-22

The objective of this work is to evaluate the mechanical properties and durability performance of bio-composite materials made from sawdust and thermoplastic polymer (HDPE). For the preparation of the composites, sawdust in different proportions with Maleic Anhydride grafted Polyethylene (MAPE) as the coupling agent was used. The thermal and mechanical properties were successively characterized. The results indicate that adding wood fillers to a polymer matrix increases the degree of crystallinity and improves the tensile strength and ductility of composites. On the contrary, resistance to water absorption decreases as a function of the wood fillers. Scanning electron microscopy (SEM) was used to analyze morphological structure alteration when exposed to intense weathering. The biodegradability of bio-composites up to 97 days was also investigated; the results indicate that, by increasing the filler content, the amount of weight loss increased as well. In other words, even though the addition of sawdust to thermoplastic polymer improves the mechanical performance of a composite material, it also accelerates the biodegradation rate of the composite. An optimum amount of filler content might compromise the effect of biodegradation and mechanical properties of composite materials.

Polypropylene film with silver nanoparticles and nanoclay aiming to action biocidal; Filme de polipropileno com nanoargila e nanoparticulas de prata visando a acao biocida

Energy Technology Data Exchange (ETDEWEB)

Oliani, W.L.; Lima, L.F.C.P.; Lugao, A.B.; Parra, D.F., E-mail: washoliani@usp.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Fermino, D.M.; Diaz, F.R.V. [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Departamento de Engenharia Metalurgica e de Materiais; Santos, P.M. dos [Universidade de Sao Paulo (USP), SP (Brazil)

2014-07-01

This paper presents an initial study of films made of polypropylene nanoclay and silver nanoparticles. The nanocomposite of polypropylene (iPP), commercial organoclay - montmorillonite (MMT), Cloisite 20A at concentrations of 1.0% and silver nanoparticles (AgNPs) at a concentration of 0.1% were prepared in a twin-screw-extruder, using polypropylene with maleic anhydride (PP-g-MA) as coupling agent. The properties of nanocomposites of PP/MMT/AgNPs are closely related to the dispersion of silver particles and the distribution of sheets of MMT in the polymer matrix, which define its efficiency in the case of the particles and their interaction clay/polymer matrix. However, this combination of MMT and AgNPs that are polar, with the polymer matrix nonpolar in the molten state, presents a challenge. The characterization of the film was performed by analysis of X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and reduction of colony forming unit (CFU %). The results indicate the formation of predominantly exfoliated microstructures and agglomeration of silver nanoparticles in the film. The effect of silver nanoparticles was evaluated against bacteria E.coli and S.aureus. (author)

Polypropylene film with silver nanoparticles and nanoclay aiming to action biocidal

International Nuclear Information System (INIS)

Oliani, W.L.; Lima, L.F.C.P.; Lugao, A.B.; Parra, D.F.; Fermino, D.M.; Diaz, F.R.V.

2014-01-01

This paper presents an initial study of films made of polypropylene nanoclay and silver nanoparticles. The nanocomposite of polypropylene (iPP), commercial organoclay - montmorillonite (MMT), Cloisite 20A at concentrations of 1.0% and silver nanoparticles (AgNPs) at a concentration of 0.1% were prepared in a twin-screw-extruder, using polypropylene with maleic anhydride (PP-g-MA) as coupling agent. The properties of nanocomposites of PP/MMT/AgNPs are closely related to the dispersion of silver particles and the distribution of sheets of MMT in the polymer matrix, which define its efficiency in the case of the particles and their interaction clay/polymer matrix. However, this combination of MMT and AgNPs that are polar, with the polymer matrix nonpolar in the molten state, presents a challenge. The characterization of the film was performed by analysis of X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and reduction of colony forming unit (CFU %). The results indicate the formation of predominantly exfoliated microstructures and agglomeration of silver nanoparticles in the film. The effect of silver nanoparticles was evaluated against bacteria E.coli and S.aureus. (author)

Evaluation of mechanical properties and durability performance of HDPE-wood composites

International Nuclear Information System (INIS)

Tazi, M.; Erchiqui, F.; Kaddami, H.; Bouazara, M.; Poaty, B.

2015-01-01

The objective of this work is to evaluate the mechanical properties and durability performance of bio-composite materials made from sawdust and thermoplastic polymer (HDPE). For the preparation of the composites, sawdust in different proportions with Maleic Anhydride grafted Polyethylene (MAPE) as the coupling agent was used. The thermal and mechanical properties were successively characterized. The results indicate that adding wood fillers to a polymer matrix increases the degree of crystallinity and improves the tensile strength and ductility of composites. On the contrary, resistance to water absorption decreases as a function of the wood fillers. Scanning electron microscopy (SEM) was used to analyze morphological structure alteration when exposed to intense weathering. The biodegradability of bio-composites up to 97 days was also investigated; the results indicate that, by increasing the filler content, the amount of weight loss increased as well. In other words, even though the addition of sawdust to thermoplastic polymer improves the mechanical performance of a composite material, it also accelerates the biodegradation rate of the composite. An optimum amount of filler content might compromise the effect of biodegradation and mechanical properties of composite materials

Modification of cellulose with succinic anhydride in TBAA/DMSO mixed solvent under catalyst-free conditions

Science.gov (United States)

Homogeneous modification of cellulose with succinic anhydride was performed in tetrabutylammonium acetate (TBAA)/dimethyl sulfoxide (DMSO) mixed solvent. The molar ratio of succinic anhydride (SA) to free hydroxyl groups in the anhydroglucose units (AGU) and TBAA dosage were investigated as paramete...

Effect of boron and phosphate compounds on physical, mechanical, and fire properties of wood-polypropylene composites

Science.gov (United States)

Nadir Ayrilmis; Turgay Akbulut; Turker Dundar; Robert H. White; Fatih Mengeloglu; Umit Buyuksari; Zeki Candan; Erkan Avci

2012-01-01

Physical, mechanical, and fire properties of the injection-molded wood flour/polypropylene composites incorporated with different contents of boron compounds; borax/boric acid and zinc borate, and phosphate compounds; mono and diammonium phosphates were investigated. The effect of the coupling agent content, maleic anhydride-grafted polypropylene, on the properties of...

Reactive compatibilization of ethylene-co-vinyl acetate/starch blends

NARCIS (Netherlands)

Ma, P.; Hristova - Bogaerds, D.G.; Schmit, P.; Goossens, J.G.P.; Lemstra, P.J.

2012-01-01

The dispersion of starch as a filler in hydrophobic ethylene-co-vinyl acetate (EVA) rubber is an issue. To obtain a fine dispersion of starch in EVA rubber, EVA/starch blends were prepared by reactive extrusion in the pres- ence of maleic anhydride (MA), benzoyl peroxide (BPO), and glycerol. MA,

Amine modified polyethylenes, prepared in near critical propane, as adhesion promoting agents in multilayered HDPE/PET films

NARCIS (Netherlands)

Gooijer, de J.M.; Scheltus, M.; Koning, C.E.

2001-01-01

High d. polyethylene (HDPE) grafted with 0.13, 0.40 and 1.04 wt% maleic anhydride (abbreviation PEMA) was modified with an excess of a variety of diamines in near crit. propane. The resulting amic acid groups were quant. imidized to the corresponding imide (PEMI) in the melt. Increasing the

Thermochemistry of sarcosine and sarcosine anhydride: Theoretical and experimental studies

International Nuclear Information System (INIS)

Amaral, Luísa M.P.F.; Santos, Ana Filipa L.O.M.; Ribeiro da Silva, Maria das Dores M.C.; Notario, Rafael

2013-01-01

Highlights: ► Study on the Energetics of the sarcosine and sarcosine anhydride. ► Experimental and computational thermochemistry of sarcosine and its anhydride. ► Ab initio calculations for two amino acid derivatives by G3(MP2)//B3LYP method. -- Abstract: The standard molar enthalpies of formation, in the gaseous phase, at T = 298.15 K, of sarcosine, −(388.0 ± 1.0) kJ · mol −1 , and sarcosine anhydride, −(334.5 ± 1.6) kJ · mol −1 , were calculated by combining, for each compound, the standard molar enthalpy of formation, in the crystalline phase, and the standard molar enthalpy of sublimation, derived from measurements of the standard massic energies of combustion by static bomb combustion calorimetry, and from measurements of vapour pressures by the Knudsen mass-loss effusion method, respectively. The standard (p o = 0.1 MPa) molar enthalpies, entropies and Gibbs functions of sublimation, at T = 298.15 K, were also calculated. A theoretical study at the G3 and G4 levels has been carried out, and the calculated enthalpies of formation have been compared with the experimental ones

On The compatibility and dynamic vulcanization of Pom/Nbr blends

International Nuclear Information System (INIS)

Mortezaee, M.; Naveed Family, M.H.; Mehrabzadeh, M.

2001-01-01

Polymer blends based on polyacetal butadiene rubber were prepared by melt blending technique. The mixing parameters such ad temperature, time and speed of mixing were varied to obtain a wide range of properties. The mixing parameters were optimized by evaluating the mechanical properties of the blend over a wide range of mixing conditions. The morphology of the blend indicated a two-phase structure. This study describes an attempt to improve the tensile strength of Pom/Nbr blends by means of compatibility and dynamic vulcanization. A commercial compatibility, maleic anhydride (Ma), has been used to control the phase morphology of the blend system. Dicumyl peroxide is used to dynamically vulcanize the Nbr elastomer in the blend. The tensile strength of the compatibility systems showed improvement. Dynamic vulcanization raises elastic recovery and tensile modulus of the blends, but the elongation at break decreases

Study of micro-phase separation of two polystyrene-based copolymer mixture using the combination of PALS and FT-IR

International Nuclear Information System (INIS)

Jiang, Z.Y.; Jiang, X.Q.; Yang, Y.X.; Huang, Y.J.; Huang, H.B.; Hsia, Y.F.

2005-01-01

Positron annihilation lifetime (PAL) spectroscopy, Fourier transform infrared (FT-IR) and differential scanning calorimetry (DSC) have been applied to study the micro-phase separation in the blends of poly(styrene-co-methylmethacrylate) (SMMA) copolymer and poly(styrene-co-maleic anhydride) (SMA) copolymer. The DSC results indicate that the SMA/SMMA blends are miscible and weak intermolecular interactions exist between SMA and SMMA. The strength of intermolecular interactions to some degree exhibits somewhat non-monotonic variation with increasing of SMA component in the blends. The results of PAL measurement present the blend containing 20 wt% SMA is phase-separated in molecular level, which is interpreted by the results of FT-IR analysis. It was concluded that it is helpful to study the miscibility of polymer blends in molecular level by means of PAL method, accompanied with the requisite measurement of DSC and FT-IR

Novel protocol for highly efficient gas-phase chemical derivatization of surface amine groups using trifluoroacetic anhydride

Science.gov (United States)

Duchoslav, Jiri; Kehrer, Matthias; Hinterreiter, Andreas; Duchoslav, Vojtech; Unterweger, Christoph; Fürst, Christian; Steinberger, Roland; Stifter, David

2018-06-01

In the current work, chemical derivatization of amine (NH2) groups with trifluoroacetic anhydride (TFAA) as an analytical method to improve the information scope of X-ray photoelectron spectroscopy (XPS) is investigated. TFAA is known to successfully label hydroxyl (OH) groups. With the introduction of a newly developed gas-phase derivatization protocol conducted at ambient pressure and using a catalyst also NH2 groups can now efficiently be labelled with a high yield and without the formation of unwanted by-products. By establishing a comprehensive and self-consistent database of reference binding energies for XPS a promising approach for distinguishing hydroxyl from amine groups is presented. The protocol was verified on different polymers, including poly(allylamine), poly(ethyleneimine), poly(vinylalcohol) and chitosan, the latter one containing both types of addressed chemical groups.

Deposition of antibacterial of poly(1,3-bis-(p-carboxyphenoxy propane)-co-(sebacic anhydride)) 20:80/gentamicin sulfate composite coatings by MAPLE

International Nuclear Information System (INIS)

Cristescu, R.; Popescu, C.; Socol, G.; Visan, A.; Mihailescu, I.N.; Gittard, S.D.; Miller, P.R.; Martin, T.N.; Narayan, R.J.; Andronie, A.; Stamatin, I.; Chrisey, D.B.

2011-01-01

We report on thin film deposition of poly(1,3-bis-(p-carboxyphenoxy propane)-co-sebacic anhydride)) 20:80 thin films containing several gentamicin concentrations by matrix assisted pulsed laser evaporation (MAPLE). A pulsed KrF* excimer laser was used to deposit the polymer-drug composite thin films. Release of gentamicin from these MAPLE-deposited polymer conjugate structures was assessed. Fourier transform infrared spectroscopy was used to demonstrate that the functional groups of the MAPLE-transferred materials were not changed by the deposition process nor were new functional groups formed. Scanning electron microscopy confirmed that MAPLE may be used to fabricate thin films of good morphological quality. The activity of gentamicin-doped films against Escherichia coli and Staphylococcus aureus bacteria was demonstrated using disk diffusion and antibacterial drop test. Our studies indicate that deposition of polymer-drug composite thin films prepared by MAPLE is a suitable technique for performing controlled drug delivery. Antimicrobial thin film coatings have several medical applications, including use for indwelling catheters and implanted medical devices.

Preparation and properties of banana fiber-reinforced composites based on high density polyethylene (HDPE)/Nylon-6 blends.

Science.gov (United States)

Liu, H; Wu, Q; Zhang, Q

2009-12-01

Banana fiber (BaF)-filled composites based on high density polyethylene (HDPE)/Nylon-6 blends were prepared via a two-step extrusion method. Maleic anhydride grafted styrene/ethylene-butylene/styrene triblock polymer (SEBS-g-MA) and maleic anhydride grafted polyethylene (PE-g-MA) were used to enhance impact performance and interfacial bonding between BaF and the resins. Mechanical, crystallization/melting, thermal stability, water absorption, and morphological properties of the composites were investigated. In the presence of SEBS-g-MA, better strengths and moduli were found for HDPE/Nylon-6 based composites compared with corresponding HDPE based composites. At a fixed weight ratio of PE-g-MA to BaF, an increase of BaF loading up to 48.2 wt.% led to a continuous improvement in moduli and flexural strength of final composites, while impact toughness was lowered gradually. Predicted tensile modulus by the Hones-Paul model for three-dimensional random fiber orientation agreed well with experimental data at the BaF loading of 29.3 wt.%. However, the randomly-oriented fiber models underestimated experimental data at higher fiber levels. It was found that the presence of SEBS-g-MA had a positive influence on reinforcing effect of the Nylon-6 component in the composites. Thermal analysis results showed that fractionated crystallization of the Nylon-6 component in the composites was induced by the addition of both SEBS-g-MA and PE-g-MA. Thermal stability of both composite systems differed slightly, except an additional decomposition peak related to the minor Nylon-6 for the composites from the HDPE/Nylon-6 blends. In the presence of SEBS-g-MA, the addition of Nylon-6 and increased BaF loading level led to an increase in the water absorption value of the composites.

Dynamic and Capillary Shear Rheology of Natural Fiber-Reinforced Composites

NARCIS (Netherlands)

Moigne, Le N.; Oever, van den M.J.A.; Budtova, T.

2013-01-01

An extended dynamic and capillary rheological study of molten flax and sisal polypropylene (PP) composites was performed. Fiber concentration varied from 20 to 50 wt% and shear rate from 0.1 rad s−1 to 10,000 s#142;−1. Maleic anhydride-grafted-PP was used as compatibilizer; it strongly reduces PP

Modification of cellulose with succinic anhydride in TBAA/DMSO mixed solvent under catalyst-free conditions

Science.gov (United States)

Ping-Ping Xin; Yao-Bing Huang; Chung-Yun Hse; Huai N. Cheng; Chaobo Huang; Hui. Pan

2017-01-01

Homogeneous modification of cellulose with succinic anhydride was performed using tetrabutylammonium acetate (TBAA)/dimethyl sulfoxide (DMSO) mixed solvent. The molar ratio of succinic anhydride (SA) to free hydroxyl groups in the anhydroglucose units (AGU), TBAA dosage, reaction temperature, and reaction time were investigated. The highest degree of substitution (DS)...

Photocurable bioactive bone cement based on hydroxyethyl methacrylate-poly(acrylic/maleic) acid resin and mesoporous sol gel-derived bioactive glass

Energy Technology Data Exchange (ETDEWEB)

Hesaraki, S., E-mail: S-hesaraki@merc.ac.ir

2016-06-01

This paper reports on strong and bioactive bone cement based on ternary bioactive SiO{sub 2}-CaO-P{sub 2}O{sub 5} glass particles and a photocurable resin comprising hydroxyethyl methacrylate (HEMA) and poly(acrylic/maleic) acid. The as-cured composite represented a compressive strength of about 95 MPa but it weakened during soaking in simulated body fluid, SBF, qua its compressive strength reached to about 20 MPa after immersing for 30 days. Biodegradability of the composite was confirmed by reducing its initial weight (~ 32%) as well as decreasing the molecular weight of early cured resin during the soaking procedure. The composite exhibited in vitro calcium phosphate precipitation in the form of nanosized carbonated hydroxyapatite, which indicates its bone bonding ability. Proliferation of calvarium-derived newborn rat osteoblasts seeded on top of the composite was observed during incubation at 37 °C, meanwhile, an adequate cell supporting ability was found. Consequently, it seems that the produced composite is an appropriate alternative for bone defect injuries, because of its good cell responses, high compressive strength and ongoing biodegradability, though more in vivo experiments are essential to confirm this assumption. - Highlights: • Light cure cement based on SiO{sub 2}-CaO-P{sub 2}O{sub 5} glass and polymer-like matrix was formed. • The matrix includes poly(acrylic/maleic acid) and poly(hydroxyethyl methacrylate). • The cement is as strong as polymethylmethacrylate bone cement. • The cement exhibits apatite formation ability in simulated body fluid. • The cement is biodegradable and supports proliferation of osteoblastic cells.

Radical coupling of maleic anhydride onto graphite to fabricate ...

Indian Academy of Sciences (India)

graphene is oxidation of graphite to graphene oxide (GO) and subsequently modification of GO with modifiers [5,6]. However, oxidation process is performed under harsh condi- tions with different oxidizing agents such ..... Sci. 87 392. [20] Nakajima T, Žemva B and Tressaud A 2000 Advanced inor- ganic fluorides: synthesis ...

Study of the dielectric properties of barium titanate-polymer composites

Energy Technology Data Exchange (ETDEWEB)

Pant, H.C. [R and D Laboratory, Defence Laboratory, Camouflage Division, Defence Laboratory Ratanada Palace, Jodhpur 342011, Rajasthan (India); Patra, M.K. [R and D Laboratory, Defence Laboratory, Camouflage Division, Defence Laboratory Ratanada Palace, Jodhpur 342011, Rajasthan (India); Verma, Aditya [R and D Laboratory, Defence Laboratory, Camouflage Division, Defence Laboratory Ratanada Palace, Jodhpur 342011, Rajasthan (India); Vadera, S.R. [R and D Laboratory, Defence Laboratory, Camouflage Division, Defence Laboratory Ratanada Palace, Jodhpur 342011, Rajasthan (India); Kumar, N. [R and D Laboratory, Defence Laboratory, Camouflage Division, Defence Laboratory Ratanada Palace, Jodhpur 342011, Rajasthan (India)]. E-mail: nkjainjd@yahoo.com

2006-07-15

A comparative study of complex dielectric properties has been carried out at the X-band of microwave frequencies of composites of barium titanate (BaTiO{sub 3}) with two different polymer matrices: insulating polyaniline (PANI) powder (emeraldine base) and maleic resin. From these studies, it is observed that the composites of BaTiO{sub 3} with maleic resin show normal composite behavior and the dielectric constant follows the asymmetric Bruggeman model. In contrast, the composites of BaTiO{sub 3} with PANI show an unusual behavior wherein even at a low concentration of PANI (5 wt.%) there is a drastic reduction in the dielectric constant of BaTiO{sub 3}. This behavior of the dielectric constant is explained on the basis of coating of BaTiO{sub 3} particles by PANI which in turn is attributed to the highly surface adsorbing character. The materials have also been characterized using Fourier transform infrared spectroscopy, powder X-ray diffraction, scanning electron microscopy and optical microscopy studies.

Properties and quality verification of biodiesel produced from tobacco seed oil

Energy Technology Data Exchange (ETDEWEB)

Usta, N., E-mail: n_usta@pau.edu.t [Pamukkale University, Mechanical Engineering Department, 20070 Denizli (Turkey); Aydogan, B. [Pamukkale University, Mechanical Engineering Department, 20070 Denizli (Turkey); Con, A.H. [Pamukkale University, Food Engineering Department, 20070 Denizli (Turkey); Uguzdogan, E. [Pamukkale University, Chemical Engineering Department, 20070 Denizli (Turkey); Ozkal, S.G. [Pamukkale University, Food Engineering Department, 20070 Denizli (Turkey)

2011-05-15

Research highlights: {yields} High quality biodiesel fuel can be produced from tobacco seed oil. {yields} Pyrogallol was found to be effective antioxidant improving the oxidation stability. {yields} The iodine number was reduced with a biodiesel including more saturated fatty acids. {yields} Octadecene-1-maleic anhydride copolymer was an effective cold flow improver. {yields} The appropriate amounts of the additives do not affect the properties negatively. -- Abstract: Tobacco seed oil has been evaluated as a feedstock for biodiesel production. In this study, all properties of the biodiesel that was produced from tobacco seed oil were examined and some solutions were derived to bring all properties of the biodiesel within European Biodiesel Standard EN14214 to verify biodiesel quality. Among the properties, only oxidation stability and iodine number of the biodiesel, which mainly depend on fatty acid composition of the oil, were not within the limits of the standard. Six different antioxidants that are tert-butylhydroquinone, butylated hydroxytoluene, propyl gallate, pyrogallol, {alpha}-tocopherol and butylated hydroxyanisole were used to improve the oxidation stability. Among them, pyrogallol was found to be the most effective antioxidant. The iodine number was improved with blending the biodiesel produced from tobacco seed oil with a biodiesel that contains more saturated fatty acids. However, the blending caused increasing the cold filter plugging point. Therefore, four different cold flow improvers, which are ethylene-vinyl acetate copolymer, octadecene-1-maleic anhydride copolymer and two commercial cold flow improvers, were used to decrease cold filter plugging point of the biodiesel and the blends. Among the improvers, the best improver is said to be octadecene-1-maleic anhydride copolymer. In addition, effects of temperature on the density and the viscosity of the biodiesel were investigated.

1-O-vinyl glycosides via Tebbe olefination, their use as chiral auxiliaries and monomers.

Science.gov (United States)

Yuan, Jialong; Lindner, Kristof; Frauenrath, Holger

2006-07-21

A series of anomerically pure 1-O-formyl glycosides 1 was prepared and converted into the corresponding 1-O-vinyl glycosides 2 by Tebbe olefination. The unsubstituted vinyl glycosides were obtained as anomerically pure compounds in good yields, and the method of preparation was compatible with the presence of a variety of functional groups. Remarkably, the anomeric formate group was regioselectively converted into the corresponding olefin in the presence of acetate and benzoate protecting groups. With the perspective to use the 1-O-vinyl glycosides as monomers for the preparation of glycosylated poly(vinyl alcohol) derivatives with controlled tacticity, their scope as chiral auxiliaries for a stereodifferentiation in addition reactions to the olefin function was investigated by using the [2+2] cycloaddition to dichloroketene as a model reaction. In particular, vinyl 2,3,4,6-tetra-O-benzoyl-alpha-d-mannopyranoside (2i) exhibited excellent diastereoselectivity. Finally, the 1-O-vinyl glycosides were successfully subjected to radical homopolymerization in bulk or used as electron-rich comonomers in radical copolymerizations with maleic anhydride, yielding alternating, glycosylated poly(vinyl alcohol-alt-maleic anhydride).

PolyMorphine: an innovative biodegradable polymer drug for extended pain relief

OpenAIRE

Rosario-Meléndez, Roselin; Harris, Carolyn L.; Delgado-Rivera, Roberto; Yu, Lei; Uhrich, Kathryn E.

2012-01-01

Morphine, a potent narcotic analgesic used for the treatment of acute and chronic pain, was chemically incorporated into a poly(anhydride-ester) backbone. The polymer termed “PolyMorphine”, was designed to degrade hydrolytically releasing morphine in a controlled manner to ultimately provide analgesia for an extended time period. PolyMorphine was synthesized via melt-condensation polymerization and its structure was characterized using proton and carbon nuclear magnetic resonance spectroscopi...

Polymers with complexing properties. Simple poly(amino acids)

Science.gov (United States)

Roque, J. M.

1978-01-01

The free amino (0.3 equiv/residue) and carboxyl (0.5 equiv/residue) groups of thermal polylysine increased dramatically on treatment with distilled water. The total hydrolysis of such a polymer was abnormal in that only about 50% of the expected amino acids were recovered. Poly (lysine-co-alanine-co-glycine) under usual conditions hydrolyzed completely in 8 hours; whereas, when it was pretreated with diazomethane, a normal period of 24 hours was required to give (nearly) the same amounts of each free amino acid as compared with those obtained from the untreated polymer. The amino groups of the basic thermal poly(amino acids) were sterically hindered. The existence of nitrogen atoms linking two or three chains and reactive groups (anhydride, imine) were proposed.

Influence of natural fibers on the phase transitions in high-density polyethylene composites using dynamic mechanical analysis

Science.gov (United States)

Mehdi Tajvidi; Robert H. Falk; John C. Hermanson; Colin Felton

2003-01-01

Dynamic mechanical analysis was employed to evaluate the performance of various natural fibers in high-density polyethylene composites. Kenaf, newsprint, rice hulls, and wood flour were sources of fiber. Composites were made at 25 percent and 50 percent by weight fiber contents. Maleic anhydride modified polyethylene was also added at 1:25 ratio to the fiber....

VOLUME 8 (2003) Sada and J. Guthrie ABSTRACT

African Journals Online (AJOL)

denise

Conjugated dienes tend to form 1:1 Diels. Alder adducts instead of copolymerizing while non - conjugated dienes can react to form 1:1 or 1:2 copolymers with vinyl groups which are cyclic15. A more extensive description of the current knowledge on the kinetics of copolymerization of maleic anhydride with dienes is found in ...

Coir fiber reinforced polypropylene composite panel for automotive interior applications

Science.gov (United States)

Nadir Ayrilmis; Songklod Jarusombuti; Vallayuth Fueangvivat; Piyawade Bauchongkol; Robert H. White

2011-01-01

In this study, physical, mechanical, and flammability properties of coconut fiber reinforced polypropylene (PP) composite panels were evaluated. Four levels of the coir fiber content (40, 50, 60, and 70 % based on the composition by weight) were mixed with the PP powder and a coupling agent, 3 wt % maleic anhydride grafted PP (MAPP) powder. The water resistance and the...

Effects of fire retardants on physical, mechanical, and fire properties of flat-pressed WPCs

Science.gov (United States)

Nadir Ayrilmis; Jan T. Benthien; Heiko Thoemen; Robert H. White

2012-01-01

Physical, mechanical, and fire properties of the flat-pressed wood plastic composites (WPCs) incorporated with various fire retardants (10% by weight) at different levels of wood flour (WF) content, 40, 50, or 60 wt%, were investigated. The WPC panels were made from dry-blended WF, polypropylene (PP), and fire retardant (FR) powders with maleic anhydride-grafted PP (2...

Dynamic mechanical analysis of compatibilizer effect on the mechanical properties of wood flour/high-density polyethylene composites

Science.gov (United States)

Mehdi Behzad; Medhi Tajvidi; Ghanbar Ehrahimi; Robert H. Falk

2004-01-01

In this study, effect of MAPE (maleic anhydride polyethylene) as the compatibilizer on the mechanical properties of wood-flour polyethylene composites has been investigated by using Dynamic Mechanical Analysis (DMA). Composites were made at 25% and 50% by weight fiber contents and 1% and 2% compatibilizer respectively. Controls were also made at the same fiber contents...

Synthesis and characterization of unsatured polyesters from the reaction of glycerol with fumaric acid

International Nuclear Information System (INIS)

Medeiros, Marina A.O.; Brioude, Michel M.; Agrela, Sara P.; Rosa, Leandro O.S.; Jose, Nadia M.; Prado, Luis A.S.A.

2009-01-01

The biodiesel production from vegetable oils has been encouraged by the Brazilian Federal Government, since biodiesel is a renewable fuel. The utilization of glycerol (by-product of biodiesel production) has gained importance, since it corresponds to 30 wt-% of the produced biodiesel. In this context, the present work aims at preparing and characterizing polymers based on glycerol, which could have an application. In this way, the production of biodiesel could be further stimulated. Unsaturated polyesters were preparing by esterification of glycerol with fumaric acid. The reaction mixture was heated up to 240 deg C. After the polymerization was complete, the material was cast onto Teflon molds. The materials were characterized by Infrared Spectroscopy, X-ray diffraction. The thermal stability was evaluated by thermogravimetric analysis and differential scanning calorimetry. The materials showed thermal stability comparable to alkyd thermoset derived from maleic anhydride and glycerol. (author)

Formaldehyde-free and thermal resistant microcapsules containing n-octadecane

International Nuclear Information System (INIS)

Shan, X.L.; Wang, J.P.; Zhang, X.X.; Wang, X.C.

2009-01-01

Microcapsules containing n-octadecane were synthesized using methacrylic acid (MAA), methyl methacrylate (MMA) and 1,4-butylene glycol diacrylate (BDDA) as shell. The surface morphology, thermal physical properties, thermal stabilities and diameter distributions of the microcapsules were investigated using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermogravimetric analysis (TG) and particle size distribution analysis, respectively. The experimental results show that, the core material is well encapsulated in the presence of emulsifier-sodium salt of styrene-maleic anhydride co-polymer. The average diameter of the microcapsules is 18 μm. The enthalpy of microencapsulated n-octadecane (MC 18 ) with MAA-MMA co-polymeric shell is 155 J g -1 which corresponds to 70 wt.% core content. The thermal resistant temperature of MC 18 is 238 o C, which is affected by n-octadecane/monomers mass ratios and the content of cross-linking agent-BDDA.

Compatibilization of recycled polymers through radiation treatment

International Nuclear Information System (INIS)

Czvikovszky, T.; Hargitai, H.

1998-01-01

Complete text of publication follows. The use of compatibilizers is crucial in composites of apolar, synthetic matrix such as PP and fibrous, polar, natural reinforcement. Radiation treatment using small EB- or gamma dose of about 8 kGy - may enhance the effect of reactive compatibilizer, involving both matrix and reinforcement into a chemically attached system. In the present work we applied byproducts of textile- and woodworking industry as reinforcing additives for polypropylene (PP), reprocessed from waste car-bumpers and recollected bottle-caps. Hemp fibers and waste-wood fibers can be mixed into the PP on a continuously operating twin-screw extruder. Various additives have been tries out in our laboratory including maleic acid anhydride, acrylic-acid grafted compatibilizers, unsaturated oligomers and vinylsilanes. The effect of different compatibilizing methods have been evaluated by comparing mechanical properties (tensile- and flexural strength, modulus of elasticity etc.), dynamic mechanical analysis (DMA) and rheological properties. The ensemble of properties is clearly enhanced by the efficient compatibilization. The reinforced - recycled products can be applied in advanced sandwich molding processing technologies of coextrusion and co-injection molding, where the dark coloured, recycled product forms the inner core of the product, covered on both side with virgin thermoplastic

Selective deoxygenation of stearic acid via an anhydride pathway

NARCIS (Netherlands)

Hollak, S.A.W.; Bitter, W.; Haveren, van J.; Es, van D.S.

2012-01-01

Stearic anhydride is proposed as reactive intermediate in the hydrogen free decarbonylation and ketonization of stearic acid over Pd/Al2O3 at 523 K. This information is crucial towards developing of a selective low temperature decarbonylation process of fatty acids towards olefins.

Synthesized cellulose/succinic anhydride as an ion exchanger. Calorimetry of divalent cations in aqueous suspension

Energy Technology Data Exchange (ETDEWEB)

Melo, Julio C.P. [Institute of Chemistry, University of Campinas, UNICAMP, P.O. Box 6154, 13084-971 Campinas, SP (Brazil); Silva Filho, Edson C. [LIMAV, Federal University of Piaui, 64049-550 Teresina, Piaui (Brazil); Santana, Sirlane A.A. [Departamento de Quimica/CCET, Universidade Federal do Maranhao, Av. dos Portugueses S/N, Campus do Bacanga, 65080-540 Sao Luiz, MA (Brazil); Airoldi, Claudio, E-mail: airoldi@iqm.unicamp.br [Institute of Chemistry, University of Campinas, UNICAMP, P.O. Box 6154, 13084-971 Campinas, SP (Brazil)

2011-09-20

Highlights: {yields} Synthetic route based on anhydride melting point. {yields} Cellulosic biopolymer/anhydride as ion exchanger. {yields} Calorimetry of cation exchange at solid/liquid interface. {yields} Favorable thermodynamic data of exchanging process. - Abstract: A synthetic route to a biopolymer/anhydride ion exchanger adds cellulose directly to molten succinic anhydride in a quasi solvent-free procedure. An amount of 3.07 {+-} 0.05 mmol of pendant groups incorporated onto the polymeric structure, which was characterized by elemental analysis, solid state carbon NMR, infrared, X-ray and thermogravimetry. The new polysaccharide is able to exchange cations from aqueous solution through a batchwise methodology, to obtain 2.46 {+-} 0.09 mmol g{sup -1} for divalent cobalt and nickel cations. The net thermal effects obtained from calorimetric titrations gave endothermic values of 3.81 {+-} 0.02 and 2.35 {+-} 0.01 kJ mol{sup -1}. The spontaneity of this ion-exchange process reflected in negative Gibbs energies and also a positive entropic contribution. These thermodynamic data at the solid/liquid interface suggests a favorable ion exchange process for this anchored biopolymer, for cation removal from the environment.

Modified Method for Detection of Benzoylecgonine in Human Urine by GC-MS: Derivatization Using Pentafluoropropanol/Acetic Anhydride.

Science.gov (United States)

Serafin, Michelle C; Paulemon, Kasandra M; Fuller, Zachary J; Bronner, William E

2017-05-01

An existing GC-MS method for detecting benzoylecgonine (BZE) in urine was modified by changing derivatizing reagents. This method modification presents a cost-effective alternative derivatization procedure for the detection of BZE in urine by GC-MS. The combination of pentafluoropropanol and acetic anhydride was found to produce the same reaction product for BZE as pentafluoropropanol with pentafluoropropionic anhydride, while reducing reagent cost. With no anhydride present, derivatization of BZE by pentafluoropropanol did not occur. Published by Oxford University Press 2017. This work is written by (a) US Government employee(s) and is in the public domain in the US.

Effect of Maleic Acid Content on the Thermal Stability, Swelling Behaviour and Network Structure of Gelatin -Based Hydrogels Prepared by Gamma Irradiation

International Nuclear Information System (INIS)

Eid, M.; Dessouki, A.M.; Abdel-Ghaffar, M.A.

2005-01-01

The preparation of highly swelling hydrogels containing diprotic acid and gelatin carried out by gamma-irradiation of acrylamide/maleic acid/gelatine/water mixture at ambient temperature. Poly (acrylamide/maleic acid/gelatin) p(AAm/MA/G) hydrogels were prepared in different MA and G contents at low dose rate (0.94 kGy/h), and moderate dose rate (3.84 kGy/h). The prepared hydrogels were confirmed by FT1R . The effect of copolymer composition, dose and dose rate on the swelling behaviour and the type of water diffusion in the network structure of the hydrogels was discussed. Increasing of MA content and G in the initial mixture leads to an increase in the amount of MA and G in the gel system and decrease in the gelation percent. The swelling behaviours of the hydrogel prepared at moderate dose rate increased with increasing MA mole content in the gel system. On the other hand, no systematic dependence of swelling on MA content was observed for the hydrogels obtained at low dose rate. Pore structure of the hydrogels was monitored by using scanning electron microscopy. Systematic swelling of P(AAm/MA/G) hydrogels prepared at moderate dose rates can be explained by the homogeneous pore size distribution of network. Thermogravimetric analysis (TGA) was employed to study the effect of network structure formation on the thermal behavior of the copolymer. To give a better understanding of the thermal stability of polymers, the rate of the thermal decomposition of P(AAm/MA/G) hydrogels has been evaluated

Effect of compatibilization and reprocessing on the isothermal crystallization kinetics of polypropylene/wood flour composites

Directory of Open Access Journals (Sweden)

Arieny Rodrigues

2013-01-01

Full Text Available Numerous studies have focused on polymer mixtures aimed at the potential applications of these materials. This work analyzed the effect of polymer reprocessing and the type and concentration of compatibilizer on the isothermal crystallization kinetics of polypropylene/wood flour composites. The composites, which were polypropylene grafted with acrylic acid (PP-g-AA and maleic anhydride (PP-g-MA, were processed in a twin screw extruder with and without compatibilizer. Reprocessed polypropylene reached complete crystallization in less time than the composites with virgin polypropylene. The addition of wood flour to the composites did not change the kinetics significantly compared to that of the pure polymers, but the compatibilizers did, particularly PP-g-AA. The nucleation exponent (n and crystallization rate (K were calculated from Avrami plots. The values of n ranged from 2 to 3, indicating instantaneous to sporadic nucleation. The crystallization half-time of reprocessed polypropylene was shorter than that of virgin polypropylene and of the compositions containing PP-g-AA compatibilizer. The activation energy of crystallization and the equilibrium melting temperature were calculated, respectively, from Arrhenius and Hoffman-Weeks plots. Both of these parameters showed lower values in the composites, particularly in the ones containing compatibilizers.

Method of solidifying radioactive laundry wastes

International Nuclear Information System (INIS)

Yasumura, Keijiro

1984-01-01

Purpose: To enable to solidify radioactive laundry wastes containing non-ionic liquid detergents less solidifiable by plastic solidification process in liquid laundry wastes for cloths or the likes discharged from a nuclear power plant. Method: Radioactive laundry wastes are solidified by using plastic solidifying agent comprising, as a main ingredient, unsaturated polyester resins and methylmethacrylate monomers. The plastic solidifying agents usable herein include, for example, unsaturated polyester resins prepared by condensating maleic anhydride and phthalic anhydride with propylene glycol and incorporated with methylmethacrylate monomers. The mixing ratio of the methylmethacrylate monomers is preferably 30 % by weight based on the unsaturated polyester resins. (Aizawa, K.)

Compatibility of anhydride cured epoxies with hexanitroazobenzene (HNAB) and hexanitrostilbene (HNS)

International Nuclear Information System (INIS)

Massis, T.M.; Wischmann, K.B.

1985-01-01

The explosives HNAB (hexanitroazobenzene) and HNS (hexanitrostilbene) have compatibility problems with amine-cured epoxy systems. A program was instituted to find compatible polymeric substitutes for use with these explosives. These polymeric materials must have rigid structures after curing for both adhesive and encapsulant applications. A promising class of epoxy materials using anhydride curing agents with various catalysts to trigger the cure reaction were developed. These polymeric systems have very good compatibility with HNS. Of those tested with HNAB, the anhydride epoxy system that used uranyl nitrate as the catalyst was found to be marginally compatible while the others were incompatible. These results indicated further studies are needed. The CRT (chemical reactivity test) was used to evaluate the compatibility of these materials. 6 references, 2 figures, 5 tables

The Causes of Blistering in Boat Building Materials

Science.gov (United States)

1986-08-01

acrylate units (MET) Ethylene glycol (MET) Propylene glycol (MET) Neopentyl glycol (NET) Maleic acid or anhydride (unsaturated) (NET) lumaric acid...PROPYLENE GLYCOL OPA ORTHOPHTHALIC ACID VINYL - URETHANE BASED POLYESTER IqPG NEOPENTYL GLYCOL RESIN EG - ETHYLENE GLYCOL TMPD - 22,, - TRiMETHY...IPA Isophthalic acid WSN Low molecular weight water soluble material NPG Neopentyl glycol OPA Orthophthalio acid PG Propylene glycol MEKP Hethyl

Fundamental Studies of Butane Oxidation over Model-Supported Vanadium Oxide Catalysts: Molecular Structure-Reactivity Relationships

NARCIS (Netherlands)

Wachs, I.E.; Jehng, J.M.; Deo, G.; Weckhuysen, B.M.; Guliants, V.V.; Benziger, J.B.; Sundaresan, S.

1997-01-01

The oxidation of n-butane to maleic anhydride was investigated over a series of model-supported vanadia catalysts where the vanadia phase was present as a two-dimensional metal oxide overlayer on the different oxide supports (TiO2, ZrO2, CeO2, Nb2O5, Al2O3, and SiO2). No correlation was found

Effect of boron compounds on physical, mechanical, and fire properties of injection molded wood plastic composites

Science.gov (United States)

Nadir Ayrilmis; Turgay Akbulut; Turker Dundar; Robert H. White; Fatih Mengeloglu; Zeki Candan; Umit Buyuksari; Erkan Avci

2011-01-01

Physical, mechanical, and fire properties of the injection-molded wood flour/polypropylene composites (WPCs) incorporated with different levels of boron compounds, borax/boric acid (BX/BA) (0.5:0.5 wt %) and zinc borate (ZB) (4, 8, or 12 wt %) were investigated. The effect of the coupling agent loading (2, 4, or 6 wt %), maleic anhydride-grafted PP (MAPP), on the...

Properties of flat-pressed wood plastic composites containing fire retardants

Science.gov (United States)

Nadir Ayrilmis; Jan. T. Benthien; Heiko Thoemen; Robert H. White

2011-01-01

This study investigated physical, mechanical, and fire properties of the flat-pressed wood plastic composites (WPCs) incorporated with various fire retardants (FRs) [5 or 15% by weight (wt)] at 50 wt % of the wood flour (WF). The WPC panels were made from dry-blended WF, polypropylene (PP) with maleic anhydride grafted PP (2 wt %), and FR powder formulations using a...

Novel Synthesis of Phytosterol Ester from Soybean Sterol and Acetic Anhydride.

Science.gov (United States)

Yang, Fuming; Oyeyinka, Samson A; Ma, Ying

2016-07-01

Phytosterols are important bioactive compounds which have several health benefits including reduction of serum cholesterol and preventing cardiovascular diseases. The most widely used method in the synthesis of its ester analogous form is the use of catalysts and solvents. These methods have been found to present some safety and health concern. In this paper, an alternative method of synthesizing phytosterol ester from soybean sterol and acetic anhydride was investigated. Process parameters such as mole ratio, temperature and time were optimized. The structure and physicochemical properties of phytosterol acetic ester were analyzed. By the use of gas chromatography, the mole ratio of soybean sterol and acetic anhydride needed for optimum esterification rate of 99.4% was 1:1 at 135 °C for 1.5 h. FTIR spectra confirmed the formation of phytosterol ester with strong absorption peaks at 1732 and 1250 cm(-1) , which corresponds to the stretching vibration of C=O and C-O-C, respectively. These peaks could be attributed to the formation of ester links which resulted from the reaction between the hydroxyl group of soybean sterol and the carbonyl group of acetic anhydride. This paper provides a better alternative to the synthesis of phytosterol ester without catalyst and solvent residues, which may have potential application in the food, health-care food, and pharmaceutical industries. © 2016 Institute of Food Technologists®

Morphology and properties of recycled polypropylene/bamboo fibers composites

International Nuclear Information System (INIS)

Phuong, Nguyen Tri; Guinault, Alain; Sollogoub, Cyrille; Chuong, Bui

2011-01-01

Polypropylene (PP) is among the most widely used thermoplastics in many industrial fields. However, like other recycled polymers, its properties usually decrease after recycling process and sometimes are degraded to poor properties level for direct re-employment. The recycled products, in general, need to be reinforced to have competitive properties. Short bamboo fibers (BF) have been added in a recycled PP (RPP) with and without compatibilizer type maleic anhydride polypropylene (MAPP). Several properties of composite materials, such as helium gas permeability and mechanical properties before and after ageing in water, were examined. The effects of bamboo fiber content and fiber chemical treatment have been also investigated. We showed that the helium permeability increases if fiber content is higher than 30% because of a poor adhesion between untreated bamboo fiber and polymer matrix. The composites reinforced by acetylated bamboo fibers show better helium permeability due to grafting of acetyl groups onto cellulose fibers surface and thus improves compatibility between bamboo fibers and matrix, which has been shown by microscopic observations. Besides, mechanical properties of composite decrease with ageing in water but the effect is less pronounced with low bamboo fiber content.

Chemical functionalization of hyaluronic acid for drug delivery applications

Energy Technology Data Exchange (ETDEWEB)

Vasi, Ana-Maria [“Gheorghe Asachi” Technical University of Iasi, Faculty of Chemical Engineering and Environmental Protection, 73 Prof. dr. docent Dimitrie Mangeron Street, 700050 Iasi (Romania); Popa, Marcel Ionel, E-mail: mipopa@ch.tuiasi.ro [“Gheorghe Asachi” Technical University of Iasi, Faculty of Chemical Engineering and Environmental Protection, 73 Prof. dr. docent Dimitrie Mangeron Street, 700050 Iasi (Romania); Butnaru, Maria [“Grigore T. Popa” University of Medicine Pharmacy, Faculty of Medical Bioengineering, 9-13 Kogalniceanu Street, 700454 Iasi (Romania); Dodi, Gianina [“Gheorghe Asachi” Technical University of Iasi, Faculty of Chemical Engineering and Environmental Protection, 73 Prof. dr. docent Dimitrie Mangeron Street, 700050 Iasi (Romania); SCIENT — Research Center for Instrumental Analysis, S.C. CROMATEC PLUS, 18 Sos. Cotroceni, 060114 Bucharest (Romania); Verestiuc, Liliana [“Grigore T. Popa” University of Medicine Pharmacy, Faculty of Medical Bioengineering, 9-13 Kogalniceanu Street, 700454 Iasi (Romania)

2014-05-01

Functionalized hyaluronic acid (HA) derivatives were obtained by ring opening mechanism of maleic anhydride (MA). FTIR and H{sup 1} NMR spectroscopy were used to confirm the chemical linkage of MA on the hyaluronic acid chains. Thermal analysis (TG-DTG and DSC) and GPC data for the new products revealed the formation of new functional groups, without significant changes in molecular weight and thermal stability. New gels based on hyaluronic acid modified derivatives were obtained by acrylic acid copolymerization in the presence of a redox initiation system. The resulted circular and interconnected pores of the gels were visualized by SEM. The release profiles of an ophthalmic model drug, pilocarpine from tested gels were studied in simulated media. Evaluation of the cytotoxicity and cell proliferation properties indicates the potential of the new systems to be used in contact with biological media in drug delivery applications. - Highlights: • New functionalized hyaluronic acid was prepared by ring opening of maleic anhydride. • Gels with circular pores based on acrylic acid copolymerization were formulated. • In vitro drug loading/release profile was evaluated in simulated ophthalmic media. • The cytotoxicity indicates the potential of derivatives to be used in vivo.

Indirect rapid prototyping of antibacterial acid anhydride copolymer microneedles

International Nuclear Information System (INIS)

Boehm, Ryan D; Miller, Philip R; Singh, Ritika; Narayan, Roger J; Shah, Akash; Stafslien, Shane; Daniels, Justin

2012-01-01

Microneedles are needle-like projections with microscale features that may be used for transdermal delivery of a variety of pharmacologic agents, including antibacterial agents. In the study described in this paper, an indirect rapid prototyping approach involving a combination of visible light dynamic mask micro-stereolithography and micromolding was used to prepare microneedle arrays out of a biodegradable acid anhydride copolymer, Gantrez® AN 169 BF. Fourier transform infrared spectroscopy, energy dispersive x-ray spectrometry and nanoindentation studies were performed to evaluate the chemical and mechanical properties of the Gantrez® AN 169 BF material. Agar plating studies were used to evaluate the in vitro antimicrobial performance of these arrays against Bacillus subtilis, Candida albicans, Enterococcus faecalis, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus. Large zones of growth inhibition were noted for Escherichia coli, S. aureus, Enterococcus faecalis and B. subtilis. The performance of Gantrez® AN 169 BF against several bacteria suggests that biodegradable acid anhydride copolymer microneedle arrays prepared using visible light dynamic mask micro-stereolithography micromolding may be useful for treating a variety of skin infections. (communication)

Investigation of the structure of isobutylene oligomers, used in the capacity of stock for succinimide additives, by the method of proton magnetic resonance

Energy Technology Data Exchange (ETDEWEB)

Iarmoliuk, V.M.; Garun, Ia.E.; Ostroverkhov, V.G.; Pustovit, V.E.; Tikhonov, V.P.

1980-01-01

By the method of proton magnetic resonance, investigation was made of the structure of hydrocarbon framework of isobutylene oligomers of the Salavatsk petrochemical plant, produced by the cation polymerization of the isobutane isobutylene fraction at a temperature from -10 to +20/sup 0/ with A1C1/sub 3/ and used in the production of succinide additives. Determination was made of the qualitative and quantitative compositions of the various structures in the oligomers. It is shown, that as a rule, oligobutenes are not pure oligomers of isobutylene, but represent, at least, fragments of four structures, which can be formed on the basis of isobutylene. The content of the given structures does not affect the reaction capacity of the oligomers in respect to the maleic anhydride. It was established, that the low molecular fraction, contained in oligomers up to 5%, are not isobutylene oligomers, but represent a low molecular polymer of butene-2 and its copolymer with isobutylene.

The influence of starch oxidization and aluminate coupling agent on interfacial interaction, rheological behavior, mechanical and thermal properties of poly(propylene carbonate)/starch blends

Science.gov (United States)

Jiang, Guo; Zhang, Shui-Dong; Huang, Han-Xiong; The Key Laboratory of Polymer Processing Engineering of the Ministry of Education Team

Poly(propylene carbonate) (PPC) is a kind of new biodegradable polymer that is synthesized by copolymerization of propylene oxide and carbon dioxide. In this work, PPC end-capped with maleic anhydride (PPCMA)/thermoplastic starch (TPS), PPCMA/thermoplastic oxidized starch (TPOS) and PPCMA/AL-TPOS (TPOS modified by aluminate coupling agent) blends were prepared by melt blending to improve its thermal and mechanical properties. FTIR results showed that there existed hydrogen-bonding interaction between PPCMA and starch. SEM observation revealed that the compatibility between PPCMA and TPOS was improved by the oxidation of starch. The enhanced interfacial interactions between PPCMA and TPOS led to a better performance of PPC blends such as storage modulus (G'), loss modulus (G''), complex viscosity (η*), tensile strength and thermal properties. Furthermore, the modification of TPOS by aluminate coupling agent (AL) facilitated the dispersion of oxidized starch in PPC matrix, and resulted in increasing the tensile strength and thermal stability. National Natural Science Foundation of China, National Science Fund of Guangdong Province.

Glycerine Treated Nanofibrillated Cellulose Composites

Directory of Open Access Journals (Sweden)

Esra Erbas Kiziltas

2016-01-01

Full Text Available Glycerine treated nanofibrillated cellulose (GNFC was prepared by mixing aqueous nanofibrillated cellulose (NFC suspensions with glycerine. Styrene maleic anhydride (SMA copolymer composites with different loadings of GNFC were prepared by melt compounding followed by injection molding. The incorporation of GNFC increased tensile and flexural modulus of elasticity of the composites. Thermogravimetric analysis showed that as GNFC loading increased, the thermal stability of the composites decreased marginally. The incorporation of GNFC into the SMA copolymer matrix resulted in higher elastic modulus (G′ and shear viscosities than the neat SMA copolymer, especially at low frequencies. The orientation of rigid GNFC particles in the composites induced a strong shear thinning behavior with an increase in GNFC loading. The decrease in the slope of elastic modulus with increasing GNFC loading suggested that the microstructural changes of the polymer matrix can be attributed to the incorporation of GNFC. Scanning electron microscopy (SEM images of fracture surfaces show areas of GNFC agglomerates in the SMA matrix.

Influence of processing conditions in PEA/organophilic clay nanocomposites

International Nuclear Information System (INIS)

Araujo, E.M.; Kojuch, L.R.; Barbosa, R.; Nobrega, K.C.; Melo, T.J.A. de

2008-01-01

Polymer/clay nanocomposites have attracted great interest from the industry as well as from the researches due to the need to obtain materials with desired properties. Nanocomposites with silicates layer represent an alternative for the conventional composites because they use a small amount of nanofiller. In this work, polyethylene/polyethylene grafted anhydride maleic (PE-g-MA)/montmorillonite clay (MMT) nanocomposites were prepared by melt intercalation in a Torque Rheometer. It was used an untreated clay (MMT) and a treated clay with the quaternary ammonium salt (OMMT). The influence of the processing conditions was evaluated, that is: 60 and 120rpm, 7 and 14 min, 190 and 220°C. The obtained systems were characterized by X-ray diffraction (XRD) and rheological behavior. The results from XRD and rheological behavior indicated that the system composed of polyethylene/PE-g-MA/OMMT presented intercalated nanocomposite structure, with larger basal distance and high viscosity, in the conditions of 120rpm and 7min, independent of temperature. (author)

A sulfonic anhydride derivative from dibenzyl trisulphide with agro-chemical activities.

Science.gov (United States)

Williams, L A D; Vasquez, E; Klaiber, I; Kraus, W; Rosner, H

2003-06-01

In the present study, the biologically active natural product dibenzyl trisulphide (DTS) which was previously isolated from the sub-tropical shrub Petiveria alliacea was transformed to methyl benzyl sulphonic anhydride (MBSA) using a "one pot" transformation method. The anhydride was evaluated for anti-microbial activities on the bacteria, Bacillus subtilis and Pseudomonas fluorescens and found to be 2.5 fold more effective than the commercial agents isoniazid and ampicillin in inhibiting the growth of B. subtilis, while on P. fluorescens it was 2.5, 5.0 and 10.0 fold more inhibitory than isoniazid, ampicillin and dibenzyl trisulphide, respectively. DTS was inactive on B. subtillis. The MIC value (microgram/spot) found for DTS on the plant pathogenic fungus, Cladosporium cucumerinum was 5.0 microgram/spot, while MBSA gave a value of 0.1 microgram/spot, compared with 1.25 and 0.16 microgram/spot for the commercial agents ketoconazole and nystatin, respectively. On the larval nematode (Meloidogyne incognita) MBSA inflicted 97.72% and 57.47% Abbotts nematicidal activities at 125.0 and 62.5 ppm, respectively, while DTS had no effect at 125.0 ppm. Nematodes which were immobilized by the low concentrations of MBSA were unable to re-activate when exposed to 10.0 ppm picrotoxin, thus suggesting that the anhydride nematicidal activity is independent of the GABA-ergic neurophysiological pathway.MBSA demonstrated a strong dose dependent radicular suppression effect (r=0.984), on the radicles of Latuca sativa germinating seeds. DTS was weakly active.

Morphological control of calcium oxalate particles in the presence of poly-(styrene-alt-maleic acid)

International Nuclear Information System (INIS)

Yu Jiaguo; Tang Hua; Cheng Bei; Zhao Xiujian

2004-01-01

Calcium oxalate (CaOx) particles exhibiting different shapes and phase structures were fabricated by a simple precipitation reaction of sodium oxalate with calcium chloride in the absence and presence of poly-(styrene-alt-maleic acid) (PSMA) as a crystal modifier at room temperature. The as-obtained products were characterized with scanning electron microscopy (SEM) and X-ray diffraction (XRD). The effects of reaction conditions including pH, [Ca 2+ ]/[C 2 O 4 2- ] ratio and concentration of PSMA and CaC 2 O 4 on the crystal forms and morphologies of the as-obtained calcium oxalate were investigated. The results show that various crystal morphologies of calcium oxalate, such as parallelograms, plates, spheres, bipyramids etc. can be obtained depending on the experimental conditions. Higher polymer concentration favors formation of the metastable calcium oxalate dihydrate (COD) crystals. Lower pH is beneficial to the formation of plate-like CaOx crystals. Especially, the monodispersed parallelogram-like CaOx crystals can be produced by PSMA as an additive at pH 2. PSMA may act as a good inhibitor for urolithiasis since it induces the formation of COD and reduces the particle size of CaOx. This research may provide new insight into the morphological control of CaOx particles and the prevention of urolithiasis

Ionic Liquids as the MOFs/Polymer Interfacial Binder for Efficient Membrane Separation.

Science.gov (United States)

Lin, Rijia; Ge, Lei; Diao, Hui; Rudolph, Victor; Zhu, Zhonghua

2016-11-23

Obtaining strong interfacial affinity between filler and polymer is critical to the preparation of mixed matrix membranes (MMMs) with high separation efficiency. However, it is still a challenge for micron-sized metal organic frameworks (MOFs) to achieve excellent compatibility and defect-free interface with polymer matrix. Thin layer of ionic liquid (IL) was immobilized on micron-sized HKUST-1 to eliminate the interfacial nonselective voids in MMMs with minimized free ionic liquid (IL) in polymer matrix, and then the obtained IL decorated HKUST-1 was incorporated into 4,4'-(hexafluoroisopropylidene)diphthalic anhydride-2,3,5,6-tetramethyl-1,3-phenyldiamine (6FDA-Durene) to fabricate MMMs. Acting as a filler/polymer interfacial binder, the favorable MOF/IL and IL/polymer interaction can facilitate the enhancement of MOF/polymer affinity. Compared to MMM with only HKUST-1 incorporation, MMM with IL decorated HKUST-1 succeeded in restricting the formation of nonselective interfacial voids, leading to an increment in CO 2 selectivity. The IL decoration method can be an effective approach to eliminate interfacial voids in MMMs, extending the filler selection to a wide range of large-sized fillers.

New polymers containing BF2-benzoylacetonate groups. Synthesis, luminescence, excimer and exciplex formation

International Nuclear Information System (INIS)

Fedorenko, Elena V.; Mirochnik, Anatolii G.; Beloliptsev, Anton Yu.

2017-01-01

In the present study, a new synthetic method for the functionalization of polystyrene (PS) and (styrene-methyl methacrylate) copolymer has been developed. Using the new method, polymers containing BF 2 -benzoylacetonate groups have been obtained through double acylation by acetic anhydride with boron trifluoride. Luminescence of the produced polymers in solutions and films has been studied. Quantum yields of polymer solution luminescence are significantly higher than those of the low-molecular-weight analog – boron difluoride benzoylacetonate. For the polymer, in which styrene fragments are separated by methyl methacrylate groups, at low concentrations of the polymer in solution one observes the monomer luminescence of BF 2 -benzoylacetonate groups, while at high concentrations – the excimer luminescence. In case of PS-based polymers, in which BF 2 -benzoylacetonate groups and phenyl rings are not separated, in diluted solutions one observes the fluorescence of the intramolecular exciplexes, while at the concentration increase – the luminescence of intermolecular exciplexes. The ability of excimer formation is responsible for the increased photostability of the produced polymers. - Highlights: •Polymers containing BF 2 -benzoylacetonate groups have been synthesized. •Luminescence of the produced polymers in solutions and films has been studied. •Formation of excimers and exciplexes in solution has been revealed. •Formation of excimers in films increases their photostability.

A novel approach in acidic disinfection through inhibition of acid resistance mechanisms; Maleic acid-mediated inhibition of glutamate decarboxylase activity enhances acid sensitivity of Listeria monocytogenes.

Science.gov (United States)

Paudyal, Ranju; Barnes, Ruth H; Karatzas, Kimon Andreas G

2018-02-01

Here it is demonstrated a novel approach in disinfection regimes where specific molecular acid resistance systems are inhibited aiming to eliminate microorganisms under acidic conditions. Despite the importance of the Glutamate Decarboxylase (GAD) system for survival of Listeria monocytogenes and other pathogens under acidic conditions, its potential inhibition by specific compounds that could lead to its elimination from foods or food preparation premises has not been studied. The effects of maleic acid on the acid resistance of L. monocytogenes were investigated and found that it has a higher antimicrobial activity under acidic conditions than other organic acids, while this could not be explained by its pKa or Ka values. The effects were found to be more pronounced on strains with higher GAD activity. Maleic acid affected the extracellular GABA levels while it did not affect the intracellular ones. Maleic acid had a major impact mainly on GadD2 activity as also shown in cell lysates. Furthermore, it was demonstrated that maleic acid is able to partly remove biofilms of L. monocytogenes. Maleic acid is able to inhibit the GAD of L. monocytogenes significantly enhancing its sensitivity to acidic conditions and together with its ability to remove biofilms, make a good candidate for disinfection regimes. Copyright © 2017 Elsevier Ltd. All rights reserved.

Self-Assembly of Telechelic Tyrosine End-Capped PEO Star Polymers in Aqueous Solution.

Science.gov (United States)

Edwards-Gayle, Charlotte J C; Greco, Francesca; Hamley, Ian W; Rambo, Robert P; Reza, Mehedi; Ruokolainen, Janne; Skoulas, Dimitrios; Iatrou, Hermis

2018-01-08

We investigate the self-assembly of two telechelic star polymer-peptide conjugates based on poly(ethylene oxide) (PEO) four-arm star polymers capped with oligotyrosine. The conjugates were prepared via N-carboxy anhydride-mediated ring-opening polymerization from PEO star polymer macroinitiators. Self-assembly occurs above a critical aggregation concentration determined via fluorescence probe assays. Peptide conformation was examined using circular dichroism spectroscopy. The structure of self-assembled aggregates was probed using small-angle X-ray scattering and cryogenic transmission electron microscopy. In contrast to previous studies on linear telechelic PEO-oligotyrosine conjugates that show self-assembly into β-sheet fibrils, the star architecture suppresses fibril formation and micelles are generally observed instead, a small population of fibrils only being observed upon pH adjustment. Hydrogelation is also suppressed by the polymer star architecture. These peptide-functionalized star polymer solutions are cytocompatible at sufficiently low concentration. These systems present tyrosine at high density and may be useful in the development of future enzyme or pH-responsive biomaterials.

Respiratory irritation by trimellitic anhydride in Brown Norway and Wistar rats

NARCIS (Netherlands)

Arts, J.H.E.; Koning, M.W.de; Bloksma, N.; Kuper, C.F.

2001-01-01

Several acid anhydrides are known for their sensitizing and irritative properties. Since both irritation and respiratory allergy can cause changes of lung function, proper testing of allergen-dependent effects on the respiratory tract requires knowledge of the respiratory irritant effects. To study

Derivatization, characterization, and tribological behavior of an amine-terminated polymer surface

International Nuclear Information System (INIS)

Ren, S.L.; Yang, S.R.; Zhao, Y.P.

2004-01-01

The derivatization, characterization, and micro-tribological behavior of an amine-terminated polymer surface were investigated. Thus, the heptafluorobutyric anhydride (HFBA) derivatized film was characterized by means of contact-angle measurement and X-ray photoelectron spectroscopy (XPS). It was found that the HFBA-derivatized film was generated on the PEI surface in the presence of a chemical amide bond. The tribological properties were characterized as well. The polymer PEI film had relative high adhesion, friction, and poor anti-wear ability, while the HFBA-derivatized polymer film possessed a very low adhesive force of only about 5.5 nN (a pyramidal Si 3 N 4 tip with radius of curvature about 50 nm was used to measure the adhesion), which was more than an order of magnitude lower than that of the silicon substrate surface. Besides, the HFBA-derivatized film registered good friction-reducing ability and thermal stability. Thus, a good alternative method was presented to improve the tribological properties of polymer film by chemisorbing molecules with low surface energy. This makes it feasible for the derivatized polymer film to find promising application in resolving the tribological problems of micro-electromechanical systems (MEMS)

Synthesis and characterization of Cis-5-Norbornene-2, 3-dicarboxylic anhydride-chitosan

International Nuclear Information System (INIS)

Ku Marshilla Ku Ishak; Zulkifli Ahmad; Hazizan Mohd Akil

2009-01-01

Chitosan was chemically modified with bulky structure, cis-5-norbornene-2, 3-dicarboxylic anhydride and the characteristic of this modified chitosan was studied. The resulting material was analyzed by FTIR, TGA, DSC, XRD and SEM to study the effect of N-acylation to the polysaccharide structure. FTIR results show that the anhydride monomer was successfully bound to amine group of chitosan. Thermal analysis of the modified structure provides the chitosan fibers with thermal stability while XRD and SEM show the lost of crystallinity of modified chitosan. XRD of modified chitosan shows broader peak pattern and a considerable increase in a dimension while SEM of chitosan presented the single particle morphology while norbornene-chitosan shows aggromolarate behaviour due to the hydrophobic nature of norbornene pendant group which induced aggromolaration of the particles in modified structure.(author)

Artemisia vulgaris pollen allergoids digestibility in the simulated conditions of the gastrointestinal tract

OpenAIRE

RATKO M. JANKOV; NATALIJA DJ. POLOVIC; MARIJA DJ. GAVROVIC-JANKULOVIC; LIDIJA BURAZER; DANICA DJERGOVIC-PETROVIC; OLGA VUCKOVIC; OLIKA DROBNJAK; ZORICA SPORCIC; MARINA ATANASKOVIC-MARKOVIC; RATKO M. JANKOV

2006-01-01

Chemically modified allergens (allergoids) have found use in both traditional and novel forms of immunotherapy of allergic disorders. Novel forms of immunotherapy include local allergen delivery, via the gastrointestinal tract. This study conveys the gastrointestinal stability of three types ofmugwort pollen allergoids under simulated conditions of the gut. Allergoids of the pollen extract of Artemisia vulgaris were obtained by means of potassium cyanate, succinic and maleic anhydride. Gastro...

Effect of material and processing parameters on mechanical properties of Polypropylene/Ethylene-Propylene-Diene-Monomer/clay nanocomposites

International Nuclear Information System (INIS)

Hejazi, Iman; Sharif, Farhad; Garmabi, Hamid

2011-01-01

Highlights: → Improved mechanical properties over a broad range of processing conditions. → Moderate levels of clay and processing parameters lead to higher toughness of TPO. → Significant improvement of tensile strength and modulus of TPO materials. -- Abstract: Polypropylene/Ethylene-Propylene-Diene-Monomer (PP/EPDM) blends are well known for having a combination of favourable mechanical properties. In this paper, addition of organoclay to PP/EPDM to make PP/EPDM nanocomposites with enhanced mechanical properties is studied. PP/EPDM/organoclay nanocomposites were prepared using a lab scale twin-screw extruder. Maleic anhydride grafted polypropylene (PP-g-MA) was used to enhance the intercalation/exfoliation process and to create good adhesion at the polymer/polymer and polymer/filler interfaces. Taguchi method was employed to deign the experiments and optimize material and processing parameters for optimized mechanical properties. Organoclay (NC) and compatibilizer content were selected as material parameters and the main processing variables were feeding rate and average shear rate (RPM). X-ray diffraction (XRD), Transmission Electron Microscopy (TEM) and Scanning Electron Microscopy (SEM) were used to study the microstructure of the nanocomposites samples. It was observed that NC content and shear rate in extruder improved the tensile strength and modulus. Another important result was the insignificant effect of NC content on impact strength while increasing shear rate first increased and then decreased the impact strength.

Effect of surfactant alkyl chain length on the dispersion, and thermal and dynamic mechanical properties of LDPE/organo-LDH composites

Directory of Open Access Journals (Sweden)

2011-05-01

Full Text Available Low density polyethylene/layered double hydroxide (LDH composites were prepared via melt compounding using different kinds of organo-LDHs and polyethylene-grafted maleic anhydride as the compatibilizer. The organo-LDHs were successfully prepared by converting a commercial MgAl-carbonate LDH into a MgAl-nitrate LDH, which was later modified by anion exchange with linear and branched sodium alkyl sulfates having different alkyl chain lengths (nc = 6, 12 and 20. It was observed that, depending on the size of the surfactant alkyl chain, different degrees of polymer chain intercalation were achieved, which is a function of the interlayer distance of the organo-LDHs, of the packing level of the alkyl chains, and of the different interaction levels between the surfactant and the polymer chains. In particular, when the number of carbon atoms of the surfactant alkyl chain is larger than 12, the intercalation of polymer chains in the interlayer space and depression of the formation of large aggregates of organo-LDH platelets are favored. A remarkable improvement of the thermal-oxidative degradation was evidenced for all of the composites; whereas only a slight increase of the crystallization temperature and no significant changes of both melting temperature and degree of crystallinity were achieved. By thermodynamic mechanical analysis, it was evidenced that a softening of the matrix is may be due to the plasticizing effect of the surfactant.

Enhanced Stability of Gold Magnetic Nanoparticles with Poly(4-styrenesulfonic acid-co-maleic acid): Tailored Optical Properties for Protein Detection

Science.gov (United States)

Zhang, Xiaomei; Zhang, Qinlu; Ma, Ting; Liu, Qian; Wu, Songdi; Hua, Kai; Zhang, Chao; Chen, Mingwei; Cui, Yali

2017-09-01

Gold magnetic nanoparticles (GoldMag) have attracted great attention due to their unique physical and chemical performances combining those of individual Fe3O4 and Au nanoparticles. Coating GoldMag with polymers not only increases the stability of the composite particles suspended in buffer but also plays a key role for establishing point-of-care optical tests for clinically relevant biomolecules. In the present paper, poly(4-styrenesulfonic acid-co-maleic acid) (PSS-MA), a negatively charged polyelectrolyte with both sulfonate and carboxylate anionic groups, was used to coat the positively charged GoldMag (30 nm) surface. The PSS-MA-coated GoldMag complex has a stable plasmon resonance adsorption peak at 544 nm. A pair of anti-D-dimer antibodies has been coupled on this GoldMag composite nanoparticle surface, and a target protein, D-dimer was detected, in the range of 0.3-6 μg/mL. The shift of the characteristic peak, caused by the assembly of GoldMag due to the formation of D-dimer-antibody sandwich bridges, allowed the detection.

Radiation grafting of acrylamide and maleic acid on chitosan and effective application for removal of Co(II) from aqueous solutions

Science.gov (United States)

Saleh, Alaaeldine Sh.; Ibrahim, Ahmed G.; Elsharma, Emad M.; Metwally, Essam; Siyam, Tharwat

2018-03-01

The graft copolymerization has been proven as a superior polymerization technique because it combines the functional advantages of the grafted and base polymers. In this work, the radiation-induced grafting of acrylamide (AAm) and maleic acid (MA) onto chitosan (CTS) was developed and optimized by determining the grafting percentage and efficiency as a function of grafting conditions such as AAm, MA, and CTS concentrations, and absorbed dose. Fourier transform infrared spectroscopic analysis (FTIR) confirmed the graft copolymerization. Thermogravimetric analysis (TGA) and differential thermal analysis (DTA) further characterized the grafted copolymers and showed their high thermal stability. Using batch sorption experiments and 60Co as a radiotracer, poly(CTS-AAm) and poly(CTS-MA) were evaluated for Co(II) removal from aqueous solutions. The Co(II) removal increases with increasing time, pH, polymer, and Co(II) concentrations. Experimentally, P(CTS-AAm) and P(CTS-MA) show high sorption capacities of Co(II), i.e. 150 mg g-1 and 421 mg g-1, respectively, which makes them potential sorbents of Co(II) for water and wastewater treatment. Finally, the Co(II) sorption was examined using sorption isotherm and kinetic models. The sorption was best fitted to Langmuir model which suggests the sorption is of chemisorption type. On the other hand, the sorption kinetics was best represented by Elovich model which also indicates the chemical nature of Co(II) sorption on P(CTS-AAm) and P(CTS-MA).

Nickel/zinc-catalyzed decarbonylative addition of anhydrides to alkynes: a DFT study.

Science.gov (United States)

Meng, Qingxi; Li, Ming

2013-10-01

Density functional theory (DFT) was used to investigate the nickel- or nickel(0)/zinc- catalyzed decarbonylative addition of phthalic anhydrides to alkynes. All intermediates and transition states were optimized completely at the B3LYP/6-31+G(d,p) level. Calculated results indicated that the decarbonylative addition of phthalic anhydrides to alkynes was exergonic, and the total free energy released was -87.6 kJ mol(-1). In the five-coordinated complexes M4a and M4b, the insertion reaction of alkynes into the Ni-C bond occurred prior to that into the Ni-O bond. The nickel(0)/zinc-catalyzed decarbonylative addition was much more dominant than the nickel-catalyzed one in whole catalytic decarbonylative addition. The reaction channel CA→M1'→T1'→M2'→T2'→M3a'→M4a'→T3a1'→M5a1' →T4a1'→M6a'→P was the most favorable among all reaction pathways of the nickel- or nickel(0)/zinc- catalyzed decarbonylative addition of phthalic anhydrides to alkynes. And the alkyne insertion reaction was the rate-determining step for this channel. The additive ZnCl2 had a significant effect, and it might change greatly the electron and geometry structures of those intermediates and transition states. On the whole, the solvent effect decreased the free energy barriers.

New polymer systems: Chain extension by dianhydrides

Science.gov (United States)

Rhein, R. A.; Ingham, J. D.

1974-01-01

Three anhydrides provide effective chain extension of hydroxy-terminated polyalkylene oxides and polybutadienes. Novel feature of these anhydride reactants is that they are difunctional as anhydrides, but they are tetrafunctional if conditions are selected that lead to total esterification or reaction of all carboxyl groups.

Fundamental investigations of clay/polymer nanocomposites and applications in co-extruded microlayered systems

Science.gov (United States)

Decker, Jeremy John

The second and fourth generations of hydroxylated dendritic polyesters (HBP2, HBP4) were combined with unmodified sodium montmorillonite clay (Na +MMT) in water to generate a broad range of polymer clay nanocomposites from 0 to 100% wt/wt Na+MMT. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were used to investigate intercalation states of the clay galleries. It was shown that interlayer spacings were independent of generation number and changed over the composition range from 0.5 nm to 3.5 nm in 0.5 nm increments that corresponded to a flattened HBP conformation within the clay tactoids. The HBP4/Na+MMT systems were investigated to study the vitrified Rigid Amorphous Fraction (RAF) induced by the clay surfaces. Differential Scanning Calorimetry (DSC) showed changes in heat capacity, Delta Cp, at Tg, that decreased with clay content, until completely suppressed at 80 wt% Na+MMT due to confinement. RAF was quantified from these changes in heat capacity and verified by the analysis of orthopositronium lifetime temperature scans utilizing positron annihilation lifetime spectroscopy (PALS): verifying the glassy nature of the RAF at elevated temperatures. Mathematical relationships allowed for correlation of the interlayer spacings with DeltaC p. RAF formation correlated to intercalated HBP4, and external surfaces of the clay tactoids. The interdiffusion of a polymer pair in microlayers was exploited to increase the concentration of nanoclay particles. When microlayers of a nanocomposite composed of organically modified montmorillonite (M2(HT)2 ) inside maleic anhydride grafted linear low-density polyethylene (LLDPE-g-MA) and low-density polyethylene (LDPE) were taken into the melt, the greater mobility of the linear LLDPE-g-MA chains compared to the branched LDPE chains caused shrinkage of the nanocomposite microlayers, concentrating the M 2(HT)2 contained within. Analysis of the clay morphology within these layers demonstrated an increase in clay

Bio-composites based on polypropylene reinforced with Almond Shells particles: Mechanical and thermal properties

International Nuclear Information System (INIS)

Essabir, H.; Nekhlaoui, S.; Malha, M.; Bensalah, M.O.; Arrakhiz, F.Z.; Qaiss, A.; Bouhfid, R.

2013-01-01

Highlights: • Almond Shells (ASs) particles have been used as reinforcement in polypropylene matrix. • The SEBS-g-MA has been used to improve the adhesion between matrix and particles. • The mechanical and thermal properties of the composite have been improved by the AS. - Abstract: In this work, Almond Shells (ASs) particles are used as reinforcement in a thermoplastic matrix as polypropylene (PP). Composites containing Almond Shells (ASs) particles with and without compatibilizer (maleic anhydride grafted polypropylene; SEBS-g-MA) for various particle content (5, 10, 15, 20, 25, 30 wt.%) was investigated by means of studying their mechanical, thermal and rheological properties. The composites were prepared in a twin-screw extruder and assessed by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), tensile testing and Dynamic Mechanical Analysis (DMA). Results show a clear improvement in mechanical and rheological properties from the use of Almond Shells particles in the matrix without and with maleic anhydride compatibilizer, corresponding to a gain in Young’s modulus of 56.2% and 35% respectively, at 30 wt.% particle loading. Thermal analysis revealed that incorporation of particle in the composites resulted in increase in the initial thermal decomposition temperatures

Radiation-curable coatings containing reactive pigment dispersants

International Nuclear Information System (INIS)

Ansel, R.E.

1985-01-01

Liquid coating compositions adapted to be cured by exposure to penetrating radiation are disclosed in which a liquid vehicle of coating viscosity having an ethylenically unsaturated portion comprising one or more polyethylenically unsaturated materials adapted to cure on radiation exposure, pigment dispersed in the vehicle, and an ethylenically unsaturated radiation-curable dispersant containing a carboxyl group for wetting the pigment and assisting in the stable dipsersion of the pigment in the vehicle. This dispersant is a half amide or half ester of an ethylenically unsaturated polycarboxylic acid anhydride, such as maleic anhydride, with an organic compound having a molecular weight of from 100 to 4000 and which contains a single hydroxy group or a single amino group as the sole reactive group thereof

Effect of maleic hydrazide and waxing on quality and shelf life of papaya (carica papaya L.) fruits

International Nuclear Information System (INIS)

Abu-Goukh, A. A.; Shattir, A. E.

2012-01-01

The effect of post harvest treatment of maleic hydrazide (MH) with and with out waxing on the quality and shelf-life of Baladi and Ekostika I papaya fruits at 18 ±1°C and 85%-90% relative humidity was evaluated. Maleic hydrazide at 250 and 500 ppm significantly delayed fruit ripening by two and three days in both papaya cultivars, respectively, compared with untreated fruits. The higher the concentration, the more was the delay in fruit ripening. The results also showed that waxing addition to MH resulted in a delay of two more days in fruit ripening that treatment with MH alone. The effect of MH and waxing treatments in delaying papaya fruits ripening was manifested in retarded respiratory climacteric, reduced weight loss and delayed fruit softening and increase in total soluble solids and ascorbic acid content.(Author)

Substituted Phthalic Anhydrides from Biobased Furanics : A New Approach to Renewable Aromatics

NARCIS (Netherlands)

Thiyagarajan, Shanmugam; Genuino, Homer C.|info:eu-repo/dai/nl/371571685; Sliwa, Michal; van der Waal, Jan C.; de Jong, Ed; van Haveren, Jacco; Weckhuysen, Bert M.|info:eu-repo/dai/nl/285484397; Bruijnincx, Pieter C. A.|info:eu-repo/dai/nl/33799529X; van Es, Daan S.

2015-01-01

A novel route for the production of renewable aromatic chemicals, particularly substituted phthalic acid anhydrides, is presented. The classical two-step approach to furanics-derived aromatics via Diels-Alder (DA) aromatization has been modified into a three-step procedure to address the general

Characterization of TPS/PHBV blends prepared in the presence of maleated PHBV

International Nuclear Information System (INIS)

Magalhaes, Natalia F.; Andrade, Cristina T.

2011-01-01

Maleated derivatives of poly(3-hydroxybutyrate-3-hydroxyvalerate) (PHBV) were obtained in an internal mixer in the presence of maleic anhydride and benzoyl peroxide, and characterized by infrared spectroscopy. Extruded blends of cornstarch and PHBV were prepared with and without the addition of maleated PHBV. Although the X-ray diffractograms had revealed decreased crystallinity, the micrographs obtained by scanning electron microscopy indicated that the addition of the maleated derivatives led to a partial compatibilization. (author)

Study of the rice husk ash utilization as filler polypropylene matrix and ionization radiation effect on this composite

International Nuclear Information System (INIS)

Alfaro, Eduardo de Faria

2010-01-01

In the first step of this work, it was evaluated the possibility of using rice husk ash as a filler in polypropylene (PP) making a comparison with talc which is the most used mineral filler in polymers. This comparison was made by using polypropylene with 20% rice husk ash as well as polypropylene with 20% talc measuring their properties. Despite the properties of the PP with 20% rice husk ash decreased compared with the composite of polypropylene with 20% talc it can be said that the rice husk ash can be used as filler for or other utilization less noble of PP . This way it is being given a destination for this residue that it is disposable in the environment contributing to its preservation, moreover reducing the product cost. This work had also as an aim to study the ionizing radiation effect in the properties of these composites. It was used the coupling agent, maleic anhydride , to verify a best sample homogenization. According to the results it can be said that PP is a semicrystalline polymer, and so it has its morphology modified when exposed to the irradiation process. This fact is due to the scission mechanisms of the polymeric chains which it is in compliance to the literature. (author)

Spray-Dried Cellulose Nanofibril-Reinforced Polypropylene Composites for Extrusion-Based Additive Manufacturing: Nonisothermal Crystallization Kinetics and Thermal Expansion

Directory of Open Access Journals (Sweden)

Lu Wang

2018-02-01

Full Text Available Isotactic polypropylene (iPP is a versatile polymer. It accounts for the second-largest polymer consumption worldwide. However, iPP is difficult to 3D print via extrusion-based processing. This is attributable to its rapid crystallization rate. In this study, spray-dried cellulose nanofibrils (SDCNF and maleic anhydride polypropylene (MAPP were investigated to reveal their effects on the nonisothermal crystallization kinetics and thermal expansion of iPP. SDCNF at 3 wt % and 30 wt % accelerated the crystallization rate of iPP, while SDCNF at 10 wt % retarded the crystallization rate by restricting crystal growth and moderately increasing the nucleation density of iPP. Additionally, adding MAPP into iPP/SDCNF composites accelerated the crystallization rate of iPP. The effective activation energy of iPP increased when more than 10 wt % SDCNF was added. Scanning electron microscopy and polarized light microscopy results indicated that high SDCNF content led to a reduced gap size among SDCNF, which hindered the iPP crystal growth. The coefficient of thermal expansion of iPP/SDCNF10% was 11.7% lower than the neat iPP. In summary, SDCNF, at 10 wt %, can be used to reduce the warping of iPP during extrusion-based additive manufacturing.

XRD study of intercalation in statically annealed composites of ethylene copolymers and organically modified montmorillonites. 2. One-tailed organoclays

Directory of Open Access Journals (Sweden)

Sara Filippi

2014-01-01

Full Text Available Ethylene copolymers with different polar comonomers, such as vinyl acetate, methyl acrylate, glycidyl methacrylate, and maleic anhydride, were used for the preparation of polymer/clay nanocomposites by statically annealing their mechanical mixtures with different commercial or home-made organically modified montmorillonites containing only one long alkyl tail. The nanostructure of the products was monitored by X-ray diffraction, and the dispersion of the silicate particles within the polymer matrix was qualitatively evaluated through microscopic analyses. The effect of the preparation conditions on the structure and the morphology of the composites was also addressed through the characterization of selected samples with similar composition prepared by melt compounding. In agreement with the findings reported in a previous paper for the composites filled with two-tailed organoclays, intercalation of the copolymer chains within the tighter galleries of the one-tailed clays occurs easily, independent of the application of a mechanical stress. However, the shear-driven break-up of the intercalated clay particles into smaller platelets (exfoliation seems more hindered. A collapse of the organoclay interlayer spacing was only observed clearly for a commercial one-tailed organoclay – Cloisite® 30B – whereas the same effect was almost negligible for a home-made organoclay with similar structure.

Thermal Properties, Structure and Morphology of Graphene Reinforced Polyethylene Terephthalate/ Polypropylene Nano composites

International Nuclear Information System (INIS)

Inuwa, I.M.; Hassan, A.; Shamsudin, S.A.

2014-01-01

In this work the thermal properties, structure and morphology of a blend of polyethylene terephthalate (PET) and polypropylene (PP) reinforced with graphene nano platelets (GNP) were investigated. A blend of PET/ PP (70/ 30 weight percent) compatibilized with styrene-ethylene-butylene-styrene grafted maleic anhydride triblock copolymer (10 phr) were fabricated by melt extrusion process in a twin screw extruder. The effective thermal conductivity of the nano composites increased as a function of the GNP concentration. More than 80 % increase in effective thermal conductivity was observed for the 7 phr reinforced sample compared to the neat blend. This observation was attributed to the development interconnected GNP sheets which formed heat conductive bridges that are suitable for maximum heat transfer. However, in the case of thermal stability which is a function of dispersibility of GNP in polymer matrix, the maximum increase was observed at 3 phr GNP loading which could be attributed to the uniform dispersion of GNPs in the matrix. It is explained that the GNP nano fillers migrated to the surface of matrix forming an effective oxygen barrier due to char formation. Morphological studies revealed uniform dispersion graphene in the polymer matrix at 3 phr GNP loading along with isolated instances of exfoliation of the graphene layers. (author)

Study of the rice husk ash utilization as filler polypropylene matrix and ionization radiation effect on this composite; Estudos da utilizacao da cinza de casca de arroz como carga em matriz de polipropileno e do efeito da radiacao ionizante sobre este composito

Energy Technology Data Exchange (ETDEWEB)

Alfaro, Eduardo de Faria

2010-07-01

In the first step of this work, it was evaluated the possibility of using rice husk ash as a filler in polypropylene (PP) making a comparison with talc which is the most used mineral filler in polymers. This comparison was made by using polypropylene with 20% rice husk ash as well as polypropylene with 20% talc measuring their properties. Despite the properties of the PP with 20% rice husk ash decreased compared with the composite of polypropylene with 20% talc it can be said that the rice husk ash can be used as filler for or other utilization less noble of PP . This way it is being given a destination for this residue that it is disposable in the environment contributing to its preservation, moreover reducing the product cost. This work had also as an aim to study the ionizing radiation effect in the properties of these composites. It was used the coupling agent, maleic anhydride , to verify a best sample homogenization. According to the results it can be said that PP is a semicrystalline polymer, and so it has its morphology modified when exposed to the irradiation process. This fact is due to the scission mechanisms of the polymeric chains which it is in compliance to the literature. (author)

A Novel Voltammetric Method for the Determination of Maleic Acid Using Silver Amalgam Paste Electrode

Czech Academy of Sciences Publication Activity Database

Niaz, A.; Fischer, J.; Barek, J.; Josypčuk, Bohdan; Sirajuddin, C.; Bhanger, M. I.

2009-01-01

Roč. 21, č. 15 (2009), s. 1719-1722 ISSN 1040-0397 R&D Projects: GA MŠk(CZ) LC06035; GA ČR GA203/07/1195 Institutional research plan: CEZ:AV0Z40400503 Keywords : voltammetry * maleic acid * silver amalgam paste electrode Subject RIV: CG - Electrochemistry Impact factor: 2.630, year: 2009

Meiotic changes in Vicia faba L. subsequent to treatments of hydrazine hydrate and maleic hydrazide

Directory of Open Access Journals (Sweden)

Shaheen Husain

2013-01-01

Full Text Available Assessing the impact of mutagens for creating variations in crops like faba bean (Vicia faba L. is an important criterion in the contemporary world where food insecurity and malnutrition is alarming at the doors of various nations. Impact of two chemical mutagens viz. hydrazine hydrate (HZ and maleic hydrazide (MH on the two varieties (NDF-1 and HB-405 of Vicia faba were analysed in terms of meiotic behavior and pollen sterility. Since there are not enough data about the effect of these mutagens on the chromosomal behaviors of Vicia faba, this study presents the role of hydrazine hydrate and maleic hydrazide as well as various types of chromosomal aberrations in crop improvement. The lower concentration of mutagens showed less pollen sterility compared to the higher concentrations. Manipulation of plant structural component to induce desirable alternations provides valuable material for the breeders and could be used favorably for increasing mutation rate and obtaining a desirable spectrum of mutation in faba beans based on preliminary studies of cell division.

New polymers containing BF{sub 2}-benzoylacetonate groups. Synthesis, luminescence, excimer and exciplex formation

Energy Technology Data Exchange (ETDEWEB)

Fedorenko, Elena V., E-mail: gev@ich.dvo.ru [Institute of Chemistry, Far Eastern Branch of the Russian Academy of Sciences, 159, Prosp. 100 letiya Vladivostoka, Vladivostok 690022 (Russian Federation); Mirochnik, Anatolii G.; Beloliptsev, Anton Yu. [Institute of Chemistry, Far Eastern Branch of the Russian Academy of Sciences, 159, Prosp. 100 letiya Vladivostoka, Vladivostok 690022 (Russian Federation)

2017-05-15

In the present study, a new synthetic method for the functionalization of polystyrene (PS) and (styrene-methyl methacrylate) copolymer has been developed. Using the new method, polymers containing BF{sub 2}-benzoylacetonate groups have been obtained through double acylation by acetic anhydride with boron trifluoride. Luminescence of the produced polymers in solutions and films has been studied. Quantum yields of polymer solution luminescence are significantly higher than those of the low-molecular-weight analog – boron difluoride benzoylacetonate. For the polymer, in which styrene fragments are separated by methyl methacrylate groups, at low concentrations of the polymer in solution one observes the monomer luminescence of BF{sub 2}-benzoylacetonate groups, while at high concentrations – the excimer luminescence. In case of PS-based polymers, in which BF{sub 2}-benzoylacetonate groups and phenyl rings are not separated, in diluted solutions one observes the fluorescence of the intramolecular exciplexes, while at the concentration increase – the luminescence of intermolecular exciplexes. The ability of excimer formation is responsible for the increased photostability of the produced polymers. - Highlights: •Polymers containing BF{sub 2}-benzoylacetonate groups have been synthesized. •Luminescence of the produced polymers in solutions and films has been studied. •Formation of excimers and exciplexes in solution has been revealed. •Formation of excimers in films increases their photostability.

Interpenetrating polymer networks based on cyanate ester and fluorinated ethynyl-terminated imide oligomers

Directory of Open Access Journals (Sweden)

Y. Wen

2017-12-01

Full Text Available Highly soluble fluorinated ethynyl-terminated imide (FETI oligomers were prepared via a conventional one-step method in m-cresol, using 4, 4′-(hexafluoroisopropylidene diphthalic anhydride and 2, 2′-bis(trifluoromethyl benzidine as the monomers, and ethynylphthalic anhydride as the end-capper; then interpenetrating polymer networks (IPN were formulated from FETI oligomers and bisphenol A dicyanate ester (BADCy through a solvent-free procedure, and their thermal, mechanical, and dielectric properties were fully characterized. The curing mechanism was studied by model reactions using nitrogen nuclear magnetic resonance. As evidenced by differential scanning calorimetry analysis and rheological measurements, the FETI/BADCy blends exhibited lower curing temperature and shorter gelation time in comparison with pure BADCy due to the catalytic effects of ethynyl and residue amic acid groups. The properties of IPNs were fully compared with those of polycyanurate, and the results revealed that the incorporation of FETI into cyanate ester resins could significantly improve the toughness, glass transition temperatures, mechanical and dielectric properties of the resultant IPNs.

Respiratory Allergy to Trimellitic Anhydride in Rats: Concentration-Response Relationships during Elicitation

NARCIS (Netherlands)

Arts, J.H.E.; Koning, M.W. de; Bloksma, N.; Kuper, C.F.

2004-01-01

The present study investigated whether airway responses of sensitized rats to trimellitic anhydride (TMA) were concentration dependent and whether these were related to irritation by TMA. Groups of BN and Wistar rats were sensitized by two dermal applications of TMA (50% w/v, followed by 25% w/v in

Compatibilization of recycled polypropylene and recycled poly (ethylene terephthalate blends with SEBS-g-MA

Directory of Open Access Journals (Sweden)

Luciana Maria Guadagnini Araujo

2018-03-01

Full Text Available Abstract The compatibilization of recycled PP/PET blend with high and low concentration (20 and 5 phr of elastomer functionalized by maleic anhydride (SEBS-g-MA was achieved. Recycled polypropylene from plastic industry and recycled PET from post-consumer bottles was used. PP/PET blends: 80:20 w/w, 50:50 w/w and 20:80 w/w were prepared in an internal mixer for mechanical properties, thermal properties, morphology and rheological properties. SEBS-g-MA promoted compatibilization of the PP/PET blends and improved their properties. With an increasing compatibilization level, the refinement of morphology was observed in the PET rich blend. Compatibilized blends showed negative deviation in the PET glass transition temperature related to neat PET, demonstrating that compatibilization was very successful. PET crystallization was accelerated in the blends due to PP presence that enhanced nucleation. It was found that the 50/50/20 blend showed huge potential for textile fiber application and that of 80/20/20 showed more intermediary properties than neat polymers.

Preparation and Characterization of Films Extruded of Polyethylene/Chitosan Modified with Poly(lactic acid

Directory of Open Access Journals (Sweden)

Jesús Manuel Quiroz-Castillo

2014-12-01

Full Text Available The use of mixtures of synthetic and natural polymers is a potential option to reduce the pollution by plastic waste. In this work, the method for the chemical modification of chitosan with poly(lactic acid was developed; then, the preparation of films of blends of polyethylene and chitosan-poly(lactic acid produced by an extrusion method using polyethylene-graft maleic anhydride as a compatibilizer. It was possible to obtain films with a maximum content of 20 wt% and 30 wt%, chitosan, with and without compatibilizer, respectively. Scanning electron microscope (SEM analysis showed a homogeneous surface on all films. The addition of the compatibilizer had a significant effect on the mechanical properties of the films, such as an increase in Young’s modulus and a decrease in the elongation at break; additionally, the compatibilizer promotes thermal degradation in a single step and gives the film a slight increase in thermal resistance. These results are attributed to an improved interaction in the interface of polyethylene and chitosan-poly(lactic acid, promoted by the compatibilizer.

Preparation and Characterization of Films Extruded of Polyethylene/Chitosan Modified with Poly(lactic acid)

Science.gov (United States)

Quiroz-Castillo, Jesús Manuel; Rodríguez-Félix, Dora Evelia; Grijalva-Monteverde, Heriberto; Lizárraga-Laborín, Lauren Lucero; Castillo-Ortega, María Mónica; del Castillo-Castro, Teresa; Rodríguez-Félix, Francisco; Herrera-Franco, Pedro Jesús

2014-01-01

The use of mixtures of synthetic and natural polymers is a potential option to reduce the pollution by plastic waste. In this work, the method for the chemical modification of chitosan with poly(lactic acid) was developed; then, the preparation of films of blends of polyethylene and chitosan-poly(lactic acid) produced by an extrusion method using polyethylene-graft maleic anhydride as a compatibilizer. It was possible to obtain films with a maximum content of 20 wt% and 30 wt%, chitosan, with and without compatibilizer, respectively. Scanning electron microscope (SEM) analysis showed a homogeneous surface on all films. The addition of the compatibilizer had a significant effect on the mechanical properties of the films, such as an increase in Young’s modulus and a decrease in the elongation at break; additionally, the compatibilizer promotes thermal degradation in a single step and gives the film a slight increase in thermal resistance. These results are attributed to an improved interaction in the interface of polyethylene and chitosan-poly(lactic acid), promoted by the compatibilizer. PMID:28787928

Toughening mechanisms in interfacially modified HDPE/thermoplastic starch blends.

Science.gov (United States)

Taguet, Aurélie; Bureau, Martin N; Huneault, Michel A; Favis, Basil D

2014-12-19

The mechanical behavior of polymer blends containing 80 wt% of HDPE and 20 wt% of TPS and compatibilized with HDPE-g-MA grafted copolymer was investigated. Unmodified HDPE/TPS blends exhibit high fracture resistance, however, the interfacial modification of those blends by addition of HDPE-g-MA leads to a dramatic drop in fracture resistance. The compatibilization of HDPE/TPS blends increases the surface area of TPS particles by decreasing their size. It was postulated that the addition of HDPE-g-MA induces a reaction between maleic anhydride and hydroxyl groups of the glycerol leading to a decrease of the glycerol content in the TPS phase. This phenomenon increases the stiffness of the modified TPS particles and stiffer TPS particles leading to an important reduction in toughness and plastic deformation, as measured by the EWF method. It is shown that the main toughening mechanism in HDPE/TPS blends is shear-yielding. This article demonstrates that stiff, low diameter TPS particles reduce shear band formation and consequently decrease the resistance to crack propagation. Copyright © 2014 Elsevier Ltd. All rights reserved.

Polyethylene organo-clay nanocomposites: the role of the interface chemistry on the extent of clay intercalation/exfoliation.

Science.gov (United States)

Mainil, Michaël; Alexandre, Michaël; Monteverde, Fabien; Dubois, Philippe

2006-02-01

High density polyethylene (HDPE)/clay nanocomposites have been prepared using three different functionalized polyethylene compatibilizers: an ethylene/vinyl acetate copolymer, a polyethylene grafted with maleic anhydride functions and a (styrene-b-ethylene/butylene-b-styrene) block copolymer. The nanocomposites were prepared via two different routes: (1) the dispersion in HDPE of a masterbatch prepared from the compatibilizer and the clay or (2) the direct melt blending of the three components. For each compatibilizer, essentially intercalated nanocomposites were formed as determined by X-ray diffraction and transmission electron microscopy. With the ethylene/vinyl acetate copolymer, a significant delamination of the intercalated clay in thin stacks was observed. This dispersion of thin intercalated stacks within the polymer matrix allowed increasing significantly the stiffness and the flame resistance of the nanocomposite. A positive effect of shear rate and blending time has also been put into evidence, especially for the process based on the masterbatch preparation, improving both the formation of thin stacks of intercalated clay and the mechanical properties and the flame resistance of the formed nanocomposites.

Antimicrobial residual effects of irrigation regimens with maleic acid in infected root canals

OpenAIRE

Ferrer-Luque, Carmen Mar?a; Gonz?lez-Castillo, Silvia; Ruiz-Linares, Matilde; Arias-Moliz, Mar?a Teresa; Rodr?guez-Archilla, Alberto; Baca, Pilar

2015-01-01

Background The success of endodontic treatment depends largely on the control of microorganisms present in infected root canals. The aim of this study was to determine the residual antimicrobial activity of several final irrigation protocols with 7% maleic acid (MA) alone and combined with chlorhexidine (CHX), cetrimide (CTR) or both, in root canals infected with Enterococcus faecalis. Biofilms of E. faecalis were grown in uniradicular roots for 4 weeks. A total of 72 specimens were divided i...

High performance maleated lignocellulose epicarp fibers for copper ion removal

OpenAIRE

Vieira,A. P.; Santana,S. A. A.; Bezerra,C. W. B.; Silva,H. A. S.; Santos,K. C. A.; Melo,J. C. P.; Silva Filho,E. C.; Airoldi,C.

2014-01-01

Natural lignocellulosic fiber epicarp extracted from the babassu coconut (Orbignya speciosa) was chemically modified through reaction with molten maleic anhydride without solvent, with incorporation of 189.34 mg g(-1) of carboxylic acid groups into the biopolymer structure. The success of this reaction was also confirmed by the presence of carboxylic acid bands at 1741 and 1164 cm(-1) in the infrared spectrum. Identically, the same group is observed through C-13 NMR CP/MAS in the solid state,...

IgG binding of mugwort pollen allergens and allergoids exposed to simulated gastrointestinal conditions measured by a self-developed ELISA test

OpenAIRE

RATKO M. JANKOV; OLGA VUCKOVIC; DANICA DJERGOVIC-PETROVIC; LIDIJA BURAZER; TANJA D. CIRKOVICVELICKOVIC; MARIJA DJ. GAVROVIC-JANKULOVIC; NATALIJA DJ. POLOVIC

2004-01-01

This study considers the influence of exposure to simulated gastrointestinal conditions (saliva, gut, intestine and acidic conditions of the gut) on IgG binding of unmodified allergens and three types of LMW allergoids of Artemisia vulgaris pollen extract obtained by means of potassium cyanate, succinic and maleic anhydride. It also concerns the optimization of a self-developed ELISA assay for comparison of the specific IgG binding of mugwort pollen extract and modified mugwort pollen derivat...

Morphology Development and Mechanical Properties Variation during Cold-Drawing of Polyethylene-Clay Nanocomposite Fibers

OpenAIRE

Bartolomeo Coppola; Paola Scarfato; Loredana Incarnato; Luciano Di Maio

2017-01-01

In this work, the influence of composition and cold-drawing on nano- and micro-scale morphology and tensile mechanical properties of PE/organoclay nanocomposite fibers was investigated. Nanocomposites were prepared by melt compounding in a twin-screw extruder, using a maleic anhydride grafted linear low density polyethylene (LLDPE–g–MA) and an organomodified montmorillonite (Dellite 67G) at three different loadings (3, 5 and 10 wt %). Fibers were produced by a single-screw extruder and drawn ...

An Examination of the Chemistry of Peroxycarboxylic Nitric Anhydrides and Related Volatile Organic Compounds During Texas Air Quality Study 2000 Using Ground-Based Measurements

Energy Technology Data Exchange (ETDEWEB)

Roberts, James M.; Jobson, B Tom T.; Kuster, W. C.; Goldan, P. D.; Murphy, Paul; Williams, Eric; Frost, G. J.; Riemer, D.; Apel, Eric; Stroud, C.; Wiedinmyer, Christine; Fehsenfeld, Fred C.

2003-08-19

Measurements of peroxycarboxylic nitric anhydrides (PANs) along with related volatile organic compounds (VOCs) were made at the La Porte super site during the TexAQS 2000 Houston study. The PAN mixing ratios ranged up to 6.5 ppbv and were broadly correlated with O3, characteristic of a highly polluted urban environment. The anthropogenic PAN homologue concentrations were generally consistent with those found in other urban environments; peroxypropionic nitric anhydride (PPN) averaged 15%, and peroxyisobutyric nitric anhydride (PiBN) averaged 3% of PAN,. Some periods were noted where local petrochemical sources resulted in anomalous PANs chemistry. This effect was especially noticeable in the case of peroxyacrylic nitric anhydride (APAN) where local sources of 1,3-butadiene and acrolein resulted in APAN as high as 30% of PAN. Peroxymethacrylic nitric anhydride (MPAN) was a fairly minor constituent of the PANs except for two periods on 4 and 5 September when air masses from high biogenic hydrocarbons (BHC) areas were observed. BHC chemistry was not a factor in the highest ozone pollution episodes in Houston but may have an impact on daily average ozone levels in some circumstances.

UV and γ-ray resistance of poly(N-methylmaleimide-alt-isobutene) and poly(diisopropyl fumarate) as transparent polymer films

Science.gov (United States)

Imaizumi, Ryota; Furuta, Masakazu; Okamura, Haruyuki; Matsumoto, Akikazu

2017-09-01

UV and γ-ray resistance of transparent polymers obtained by radical polymerization of maleic and fumaric acid derivatives, i.e., an alternating copolymer of N-methylmaleimide and isobutene (PMI) and poly(diisopropyl fumarate) (PDiPF), was investigated. Transmittance in UV and visible regions of these polymers were examined after UV irradiation and compared with the results for poly(methyl methacrylate) (PMMA) and polycarbonate (PC) as conventional transparent polymers. The order of stability toward UV irradiation was PMMA≈PDiPF>PMI>>PC, deduced from changes in the transmittance of 380 nm light. Tensile mechanical properties, such as elastic modulus, maximum strength, and elongation values of PMI, PDiPF, and PMMA were also investigated after UV and γ-radiation. UV irradiation induced the side chain scission of PMI and PDiPF via Norrish I type reaction as well as crosslinking by combination between formed polymer radicals, leading to deterioration in their optical and mechanical properties. γ-radiation induced significant changes in molecular weight and mechanical properties of the polymers. In conclusion, PMI exhibited unchanged mechanical properties and PDiPF maintained its high transparency under various irradiation conditions.

NIOSH Manual of Analytical Methods (third edition). Fourth supplement

Energy Technology Data Exchange (ETDEWEB)

1990-08-15

The NIOSH Manual of Analytical Methods, 3rd edition, was updated for the following chemicals: allyl-glycidyl-ether, 2-aminopyridine, aspartame, bromine, chlorine, n-butylamine, n-butyl-glycidyl-ether, carbon-dioxide, carbon-monoxide, chlorinated-camphene, chloroacetaldehyde, p-chlorophenol, crotonaldehyde, 1,1-dimethylhydrazine, dinitro-o-cresol, ethyl-acetate, ethyl-formate, ethylenimine, sodium-fluoride, hydrogen-fluoride, cryolite, sodium-hexafluoroaluminate, formic-acid, hexachlorobutadiene, hydrogen-cyanide, hydrogen-sulfide, isopropyl-acetate, isopropyl-ether, isopropyl-glycidyl-ether, lead, lead-oxide, maleic-anhydride, methyl-acetate, methyl-acrylate, methyl-tert-butyl ether, methyl-cellosolve-acetate, methylcyclohexanol, 4,4'-methylenedianiline, monomethylaniline, monomethylhydrazine, nitric-oxide, p-nitroaniline, phenyl-ether, phenyl-ether-biphenyl mixture, phenyl-glycidyl-ether, phenylhydrazine, phosphine, ronnel, sulfuryl-fluoride, talc, tributyl-phosphate, 1,1,2-trichloro-1,2,2-trifluoroethane, trimellitic-anhydride, triorthocresyl-phosphate, triphenyl-phosphate, and vinyl-acetate.

Orientation phenomena in chromophore DR1-containing polymer films and their non-linear optical response

International Nuclear Information System (INIS)

Moencke, Doris; Mountrichas, Grigoris; Pispas, Stergios; Kamitsos, Efstratios I.

2011-01-01

The effectiveness of chromophore alignment in polymer films following corona poling can be assessed by the generated second harmonic signal. Optimization of the stability and strength of this nonlinear optical response may improve with a better understanding of the underlying principal order phenomena. Structural analysis by vibrational, optical, and 1 H NMR spectroscopy reveals side chain tacticity, aggregation effects, and changes in orientation as a function of temperature. Co-polymers with the functionalized chromophore Disperse Red 1 methacrylate (MDR1) were prepared for three different methacrylate types. High side chain polarity and short side chain length increase generally chromophore aggregation in films, whereas the very long poly-ether side chains in PMEO based co-polymers are wrapped separately around the DR1 entities. Side chain tacticity depends on space requirements, but also on the capacity of side groups to form OH-bridges. Side chain tacticity might present an additional parameter for the assessment of chromophore aggregation and poling induced alignments. Stepwise heating of co-polymer films causes an increase in the number of random over ordered side chain arrangements. Cross-linking by anhydride formation is observed after heating the methacrylic acid based co-polymer.

Structural Analysis of Aromatic Liquid Crystalline Polyesters

Directory of Open Access Journals (Sweden)

Arpad Somogyi

2011-01-01

Full Text Available Laboratory preparations of liquid crystalline prepolymers, distillates accompanying prepolymers, final polymers, and sublimates accompanying final polymers were examined. NaOD/D2O depolymerization of prepolymers and polymers back to monomers with integration of the 1H NMR spectra showed up to 6% excess of carboxyls over phenol groups, caused partly by loss of the low-boiling comonomer hydroquinone through distillation during prepolymerization and leaving anhydride units in the polymer chain. ESI− MS and MS/MS of hexafluoroisopropanol extracts of the prepolymer detected small molecules including some containing anhydride groups; ESI+ MS showed the presence of small cyclic oligomers. 1H NMR (including TOCSY spectra provided more quantitative analyses of these oligomers. The final polymerization increases the length of the polymer chains and sublimes out the small oligomers. Anhydride linkages remaining in the polymer must make LCP’s more susceptible to degradation by nucleophilic reagents such as water, alkalis, and amines.

Maleic acid and aluminum chloride catalyzed conversion of glucose to 5-(hydroxymethyl) furfural and levulinic acid in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Zhang, Ximing [Laboratory of Renewable Resources Engineering and Department of Agricultural and Biological Engineering; Purdue University; West Lafayette; USA; The Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio); Murria, Priya [The Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio); Discovery Park; Purdue University; West Lafayette; USA; Jiang, Yuan [The Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio); Discovery Park; Purdue University; West Lafayette; USA; Xiao, Weihua [Laboratory of Renewable Resources Engineering and Department of Agricultural and Biological Engineering; Purdue University; West Lafayette; USA; College of Engineering; Kenttämaa, Hilkka I. [The Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio); Discovery Park; Purdue University; West Lafayette; USA; Abu-Omar, Mahdi M. [The Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio); Discovery Park; Purdue University; West Lafayette; USA; Mosier, Nathan S. [Laboratory of Renewable Resources Engineering and Department of Agricultural and Biological Engineering; Purdue University; West Lafayette; USA; The Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio)

2016-01-01

Maleic acid (MA) and AlCl₃self-assemble into catalytic complexes (Al–(MA)₂–(OH)₂(aq)) with improved selectivity for converting glucose to HMF, and levulinic acid.

Importance of relative humidity in the oxidative ageing of organic aerosols: case study of the ozonolysis of maleic acid aerosol

Directory of Open Access Journals (Sweden)

P. J. Gallimore

2011-12-01

Full Text Available Many important atmospheric aerosol processes depend on the chemical composition of the aerosol, e.g. water uptake and particle cloud interactions. Atmospheric ageing processes, such as oxidation reactions, significantly and continuously change the chemical composition of aerosol particles throughout their lifetime. These ageing processes are often poorly understood. In this study we utilize an aerosol flow tube set up and an ultra-high resolution mass spectrometer to explore the effect of relative humidity (RH in the range of <5–90% on the ozonolysis of maleic acid aerosol which is employed as model organic aerosol system. Due to the slow reaction kinetics relatively high ozone concentrations of 160–200 ppm were used to achieve an appreciable degree of oxidation of maleic acid. The effect of oxidative ageing on the hygroscopicity of maleic acid particles is also investigated using an electrodynamic balance and thermodynamic modelling. RH has a profound effect on the oxidation of maleic acid particles. Very little oxidation is observed at RH < 50% and the only observed reaction products are glyoxylic acid and formic acid. In comparison, when RH > 50% there are about 15 oxidation products identified. This increased oxidation was observed even when the particles were exposed to high humidities long after a low RH ozonolysis reaction. This result might have negative implications for the use of water as an extraction solvent for the analysis of oxidized organic aerosols. These humidity-dependent differences in the composition of the ozonolyzed aerosol demonstrate that water is both a key reactant in the oxidation scheme and a determinant of particle phase and hence diffusivity. The measured chemical composition of the processed aerosol is used to model the hygroscopic growth, which compares favourably with water uptake results from the electrodynamic balance measurements. A reaction mechanism is presented which takes into account the RH dependent

Evaluation of mechanical and thermal properties of Pine cone fibers reinforced compatibilized polypropylene

International Nuclear Information System (INIS)

Arrakhiz, F.Z.; El Achaby, M.; Benmoussa, K.; Bouhfid, R.; Essassi, E.M.; Qaiss, A.

2012-01-01

Highlights: ► Pine cone fibers are used as reinforcement in thermoplastic matrix. ► Pine cone fiber was alkali treated to remove waxes and non cellulosic component. ► Fiber–matrix adhesion was assured by the use of a SEBS-g-MA as a compatibilizer. -- Abstract: Pine cone fibers are a cellulosic material readily available and can be used as reinforcement in a thermoplastic-based composite. A solid knowledge of their fibrillar morphology and structure is required to evaluate their usefulness as a substitute to other abundant natural fibers. Pine cone fibers were alkali treated prior usage to remove waxes and non cellulosic surface component. Fiber–matrix adhesion was assured by both a styrene–(ethylene–butene)–styrene triblock copolymer grafted with maleic anhydride (SEBS-g-MA) and a linear block copolymer based on styrene and butadiene compatibilizer. Scanning Electron Microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction, Thermogravimetric analysis (TGA), tensile and torsional tests were employed for Pine cone polypropylene composite and compatibilized composite at different fiber content. Results show a clear improvement in mechanical properties from the use of both alkali treated Pine cone and Pine cone compatibilized with maleic anhydride, a gain of 43% and 49% respectively in the Young’s modulus, as a results of improved adhesion between fibers and matrix at the interface.

Chemical radiolabeling of carboxyatractyloside by [14C]acetic anhydride

International Nuclear Information System (INIS)

Block, M.R.; Pougeois, R.; Vignais, P.V.

1980-01-01

The authors report the synthesis and biological properties of a radiolabeled derivative of CAT obtained with acetylation of the primary alcohol of CAT with radiolabeled acetic anhydride. They also investigate the question of mutual exclusion of CAT and BA for binding to the mitochondrial ADP/ATP carrier in double labeling experiments based on the use of [ 3 H]BA and [ 14 C]Ac-CAT. The results are consistent with the view that the ADP/ATP carrier possesses two separate interacting binding sites for AT (or CAT) and for BA. (Auth.)

Syntheses, structures, and magnetic properties of cobalt(II) and nickel(II) coordination polymers based on a V-shaped ligand

Energy Technology Data Exchange (ETDEWEB)

Yao, Shuang [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); Yi, Fei-Yan [The School of Materials Science and Chemical Engineering, Ningbo University, Ningbo 315211 (China); Li, Guanghua [State Key Laboratory of Inorganic Synthesis & Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012 (China); Yu, Yang [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); Wang, Jing-yuan, E-mail: jywang@mail.ipc.ac.cn [Technical Institute of Physics and Chemistry of the Chinese Academy of Sciences, 29 Zhongguancun East Road, Haidian District, Beijing 100190 (China); Liu, Dan, E-mail: liudan2007@ciac.ac.cn [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); Song, Shu-Yan [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China)

2017-06-15

Two coordination polymers [Co{sub 2}(TA)(4,4′-bipy){sub 2}(H{sub 2}O){sub 2}]·H{sub 2}O (1) and [Ni{sub 2}(TA)(4,4′-bipy){sub 2}(H{sub 2}O){sub 4}]·3H{sub 2}O (2) were prepared by hydrothermal reactions of MCl{sub 2}·6H{sub 2}O (M = Co, Ni) with a V-shaped ligand TDPA (3,3′,4,4′-thiodiphthalic anhydride) and a I-shaped N-donor co-ligand (4,4′-bipy). They were characterized by elemental analyses, thermogravinetric analyses, and magnetic behavior. As is expected, TDPA hydrolyzes into the corresponding tetra-carboxylate acid H{sub 4}TA (3,3′,4,4′-thiodiphthalic acid) during the reactions. Co{sub 2} dimer and Ni mononuclear center are connected into two-dimensional (2D) layers by H{sub 4}TA and 4,4′-bipy bridge in 1 and 2, respectively. The most amazing feature is that 1 and 2 exhibit interesting spin-canting metamagnetism and weak ferromagnetic behavior, respectively, with the critical Néel temperature of T{sub N} =4 K for 1 and T{sub N} =13 K for 2, based on variable temperature magnetic susceptibility measurements. In low mono- or dinuclear metal system, such magnetic behaviors have rare been observed. Furthermore, complex 1 will be a potential metamagnet material. - Graphical abstract: Two Co(II) and Ni(II) coordination polymers were synthesized by hydrothermal reactions from a V-shape ligand (3,3′,4,4′-thiodiphthalic anhydride) and a I-shape ligand (4,4′-bipy), which were characterized by single crystal X-ray diffraction, elemental analyses, thermogravinetric analyses, and magnetic behavior, and exhibit interesting spin-canting metamagnetism and weak ferromagnetic behavior, respectively. - Highlights: • Two Co(II) and Ni(II) coordination polymers were successfully synthesized. • Co(II) coordination polymer shows an interesting spin-canting metamagnetism. • Ni(II) coordination polymer exhibits a weak ferromagnetic behavior.

Application of the photo-fenton process to the mineralization of phthalic anhydride in aqueous medium

International Nuclear Information System (INIS)

Trabelsi Souissi, Souhaila; Oturan, N.; Oturan, M. A; Bellakhal, N.

2009-01-01

A photochemical method for the oxidation of persistent organic pollutants (POPs) present in liquid effluents of plastic industry is described. This method, called p hoto-Fenton , involves the generation of hydroxyl radicals by coupling the Fenton reaction and photochemistry, .OH radicals thus formed react rapidly with organic pollutants leading to their oxidation until their total mineralization. In this study, we applied the photo-Fenton process for the removal of phthalic anhydride (plasticizer). In this way, an optimization of experimental parameters (namely the ratio R = [H 2 O 2 ]/[Fe 3+ ] and Fe 3+ initial concentration) was performed. Under optimal conditions, the kinetic of mineralization of phthalic anhydride by .OH has been studied. All results confirm the efficiency of photo-Fenton process for the decontamination of liquid effluents loaded with plasticizers.

PolyMorphine: an innovative biodegradable polymer drug for extended pain relief.

Science.gov (United States)

Rosario-Meléndez, Roselin; Harris, Carolyn L; Delgado-Rivera, Roberto; Yu, Lei; Uhrich, Kathryn E

2012-09-28

Morphine, a potent narcotic analgesic used for the treatment of acute and chronic pain, was chemically incorporated into a poly(anhydride-ester) backbone. The polymer termed "PolyMorphine", was designed to degrade hydrolytically releasing morphine in a controlled manner to ultimately provide analgesia for an extended time period. PolyMorphine was synthesized via melt-condensation polymerization and its structure was characterized using proton and carbon nuclear magnetic resonance spectroscopies, and infrared spectroscopy. The weight-average molecular weight and the thermal properties were determined. The hydrolytic degradation pathway of the polymer was determined by in vitro studies, showing that free morphine is released. In vitro cytocompatibility studies demonstrated that PolyMorphine is non-cytotoxic towards fibroblasts. In vivo studies using mice showed that PolyMorphine provides analgesia for 3 days, 20 times the analgesic window of free morphine. The animals retained full responsiveness to morphine after being subjected to an acute morphine challenge. Copyright © 2012 Elsevier B.V. All rights reserved.

Can thiolation render a low molecular weight polymer of just 20-kDa mucoadhesive?

Science.gov (United States)

Mahmood, Arshad; Bonengel, Sonja; Laffleur, Flavia; Ijaz, Muhammad; Idrees, Muneeb Ahmad; Hussain, Shah; Huck, Christian W; Matuszczak, Barbara; Bernkop-Schnürch, Andreas

2016-01-01

The objective was to investigate whether even low-molecular weight polymers (LMWPs) can be rendered mucoadhesive due to thiolation. Interceded by the double catalytic system carbodiimide/N-hydroxysuccinimide, cysteamine was covalently attached to a copolymer, poly(4-styrenesulfonic acid-co-maleic acid) (PSSA-MA) exhibiting a molecular weight of just 20 kDa. Depending on the amount of added N-hydroxysuccinimide and cysteamine, the resulting PSSA-MA-cysteamine (PC) conjugates exhibited increasing degree of thiolation, highest being "PC 2300" exhibiting 2300.16 ± 149.86 μmol thiol groups per gram of polymer (mean ± SD; n = 3). This newly developed thiolated polymer was evaluated regarding mucoadhesive, rheological and drug release properties as well from the toxicological point of view. Swelling behavior in 100 mM phosphate buffer pH 6.8 was improved up to 180-fold. Furthermore, due to thiolation, the mucoadhesive properties of the polymer were 240-fold improved. Rheological measurements of polymer/mucus mixtures confirmed results obtained by mucoadhesion studies. In comparison to unmodified polymer, PC 2300 showed 2.3-, 2.3- and 2.4-fold increase in dynamic viscosity, elastic modulus and viscous modulus, respectively. Sustained release of the model drug codeine HCl out of the thiomer was provided for 2.5 h (p polymer. Moreover, the thiomer was found non-toxic over Caco-2 cells for a period of 6- and 24-h exposure. Findings of the present study provide evidence that due to thiolation LMWPs can be rendered highly mucoadhesive as well as cohesive and that a controlled drug release out of such polymers can be provided.

Continuous Preparation of 1:1 Haloperidol-Maleic Acid Salt by a Novel Solvent-Free Method Using a Twin Screw Melt Extruder.

Science.gov (United States)

Lee, Hung Lin; Vasoya, Jaydip M; Cirqueira, Marilia de Lima; Yeh, Kuan Lin; Lee, Tu; Serajuddin, Abu T M

2017-04-03

Salts are generally prepared by acid-base reaction in relatively large volumes of organic solvents, followed by crystallization. In this study, the potential for preparing a pharmaceutical salt between haloperidol and maleic acid by a novel solvent-free method using a twin-screw melt extruder was investigated. The pH-solubility relationship between haloperidol and maleic acid in aqueous medium was first determined, which demonstrated that 1:1 salt formation between them was feasible (pH max 4.8; salt solubility 4.7 mg/mL). Extrusion of a 1:1 mixture of haloperidol and maleic acid at the extruder barrel temperature of 60 °C resulted in the formation of a highly crystalline salt. The effects of operating temperature and screw configuration on salt formation were also investigated, and those two were identified as key processing parameters. Salts were also prepared by solution crystallization from ethyl acetate, liquid-assisted grinding, and heat-assisted grinding and compared with those obtained by melt extrusion by using DSC, PXRD, TGA, and optical microscopy. While similar salts were obtained by all methods, both melt extrusion and solution crystallization yielded highly crystalline materials with identical enthalpies of melting. During the pH-solubility study, a salt hydrate form was also identified, which, upon heating, converted to anhydrate similar to that obtained by other methods. There were previous reports of the formation of cocrystals, but not salts, by melt extrusion. 1 H NMR and single-crystal X-ray diffraction confirmed that a salt was indeed formed in the present study. The haloperidol-maleic acid salt obtained was nonhygroscopic in the moisture sorption study and converted to the hydrate form only upon mixing with water. Thus, we are reporting for the first time a relatively simple and solvent-free twin-screw melt extrusion method for the preparation of a pharmaceutical salt that provides material comparable to that obtained by solution

Effect of maleic acid content on the thermal stability, swelling behaviour and network structure of gelatin-based hydrogels prepared by gamma irradiation

Energy Technology Data Exchange (ETDEWEB)

Eid, M. [National Center For Radiation Research and Technology, P.O. Box 29, Nasr City, Cairo 11731 (Egypt)], E-mail: mona_eid2000@yahoo.com; Abdel-Ghaffar, M.A. [National Research Center, Dokki, Cairo (Egypt); Dessouki, A.M. [National Center For Radiation Research and Technology, P.O. Box 29, Nasr City, Cairo 11731 (Egypt)

2009-01-15

The highly swelling Poly (acrylamide/maleic acid/gelatin) P(AAm/MA/G) hydrogels were prepared by gamma-irradiation at low dose rate (0.94 kGy/h) and moderate dose rate (3.84 kGy/h). The hydrogels were confirmed by FTIR. The effect of copolymer composition, dose and dose rate on the swelling behaviour was discussed. Increasing of MA content and G in the initial mixture leads to an increase in the amount of MA and G in the gel system and decrease in the gelation %. The swelling behaviours of the hydrogel prepared at moderate dose rate increased with increasing MA mole content in the gel system but, there is no systematic dependence of swelling on MA content was observed for the hydrogels obtained at low dose rate. Pore structure of the hydrogels was monitored by using scanning electron microscopy. Thermogravimetric analysis (TGA) and the rate of the thermal decomposition of P(AAm/MA/G) hydrogels has been evaluated to give a better understanding of the thermal stability of polymers, The X-ray data of P(AAm/MA/G) hydrogels was discussed to investigate some features namely the degree of ordering and crystallite size.

Influence of reaction medium during synthesis of Gantrez AN 119 nanoparticles for oral vaccination.

Science.gov (United States)

Vandamme, Katrien; Melkebeek, Vesna; Cox, Eric; Deforce, Dieter; Lenoir, Joke; Adriaens, Els; Vervaet, Chris; Remon, Jean Paul

2010-02-01

Two synthesis methods of poly(methyl vinyl ether-co-maleic anhydride) (Gantrez AN 119) nanoparticles (NP) (used for oral vaccination) were compared. Wheat germ agglutinin (WGA) was used as ligand to enhance the bioadhesive properties of NP and beta-galactosidase as antigen. The first method encapsulated beta-galactosidase in NP by co-precipitation in an acetone/water mixture containing 44% acetone. In the second method, antigen addition occurred in 100% acetone. To improve stability, NP were crosslinked with 1,3-diaminopropane. The stability of WGA-conjugated NP with encapsulated antigen diminished at lower pH and when decreasing the amount of crosslinker. The binding type between WGA and polymer depended on the synthesis method: predominantly ionic bonds were formed using the 44% acetone method, whereas synthesis via the 100% acetone method resulted in covalent bonds. The biological activity of the WGA coating, evaluated via a pig gastric mucin binding test, was lower in NP prepared via the 100% acetone method. No release of native antigen was detected after hydrolysis of NP, due to the covalent antigen binding during antigen encapsulation and the high reactivity of the polymer. Moreover, the mucosal irritation capacity was evaluated upon nanoparticle hydrolysis using a slug mucosal irritation assay. Herein, hydrolysed NP of the 44% acetone method were classified as mild irritative. Copyright (c) 2009 Elsevier B.V. All rights reserved.

Efficient photochemical generation of peroxycarboxylic nitric anhydrides with ultraviolet light-emitting diodes

Science.gov (United States)

Rider, N. D.; Taha, Y. M.; Odame-Ankrah, C. A.; Huo, J. A.; Tokarek, T. W.; Cairns, E.; Moussa, S. G.; Liggio, J.; Osthoff, H. D.

2015-07-01

Photochemical sources of peroxycarboxylic nitric anhydrides (PANs) are utilized in many atmospheric measurement techniques for calibration or to deliver an internal standard. Conventionally, such sources rely on phosphor-coated low-pressure mercury (Hg) lamps to generate the UV light necessary to photo-dissociate a dialkyl ketone (usually acetone) in the presence of a calibrated amount of nitric oxide (NO) and oxygen (O2). In this manuscript, a photochemical PAN source in which the Hg lamp has been replaced by arrays of ultraviolet light-emitting diodes (UV-LEDs) is described. The output of the UV-LED source was analyzed by gas chromatography (PAN-GC) and thermal dissociation cavity ring-down spectroscopy (TD-CRDS). Using acetone, diethyl ketone (DIEK), diisopropyl ketone (DIPK), or di-n-propyl ketone (DNPK), respectively, the source produces peroxyacetic (PAN), peroxypropionic (PPN), peroxyisobutanoic (PiBN), or peroxy-n-butanoic nitric anhydride (PnBN) from NO in high yield (> 90 %). Box model simulations with a subset of the Master Chemical Mechanism (MCM) were carried out to rationalize product yields and to identify side products. The present work demonstrates that UV-LED arrays are a viable alternative to current Hg lamp setups.

Partial oxidation of n- and i-pentane over promoted vanadium-phosphorus oxide catalysts

Energy Technology Data Exchange (ETDEWEB)

Zazhigalov, V.A.; Mikhajluk, B.D.; Komashko, G.A. [AN Ukrainskoj SSR, Kiev (Ukraine). Inst. Fizicheskoj Khimii

1998-12-31

It is known, that the cost of raw materials for catalytic oxidation processes is about 60% of the product price. Cheap initial compounds to produce variety of products and to replace olefins and aromatic hydrocarbons are paraffins. That is why catalytic systems which could be possibly rather efficient in selective oxidation of paraffin hydrocarbons are under very close investigation now. One of such processes in n-pentane oxidation. The obtained results on n-pentane oxidation over VPO catalysts were quite encouraging in respect of possible reach high selectivity and yield of phthalic anhydride. However, in our work it was shown that the main product of n-pentane oxidation in the presence of VPO catalytic system as well as VPMeO was maleic anhydride. Some later our results were confirmed in, where to grow the selectivity towards phthalic anhydride the Co-additive was introduced. On the basis of the proposal made before on the mechanism of paraffins conversion over the vanadyl pyrophosphate surface with their activation at the first and fourth carbon atoms, we assumed possible methylmaleic (citraconic) anhydride forming at n- and i-pentane oxidation. This assumption has been recently supported by both our and other researchers` experimental results. In it was also hypothized possible mechanistic features for phthalic anhydride forming from n-pentane. The present work deals with the results of n- and i-pentane oxidation over VPO catalysts promoted with Bi, Cs, Te, Zr. (orig.)

Light-Induced C-H Arylation of (Hetero)arenes by In Situ Generated Diazo Anhydrides.

Science.gov (United States)

Cantillo, David; Mateos, Carlos; Rincon, Juan A; de Frutos, Oscar; Kappe, C Oliver

2015-09-07

Diazo anhydrides (Ar-N=N-O-N=N-Ar) have been known since 1896 but have rarely been used in synthesis. This communication describes the development of a photochemical catalyst-free C-H arylation methodology for the preparation of bi(hetero)aryls by the one-pot reaction of anilines with tert-butyl nitrite and (hetero)arenes under neutral conditions. The key step in this procedure is the in situ formation and subsequent photochemical (>300 nm) homolytic cleavage of a transient diazo anhydride intermediate. The generated aryl radical then efficiently reacts with a (hetero)arene to form the desired bi(hetero)aryls producing only nitrogen, water, and tert-butanol as byproducts. The scope of the reaction for several substituted anilines and (hetero)arenes was investigated. A continuous-flow protocol increasing selectivity and safety has been developed enabling the experimentally straightforward preparation of a variety of substituted bi(hetero)aryls within 45 min of reaction time. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Effects of electron-beam irradation on some structural properties of granulated polymer blends

International Nuclear Information System (INIS)

Zenkiewicz, Marian; Czuprynska, Joanna; Polanski, Julian; Karasiewicz, Tomasz; Engelgard, Wlodzimierz

2008-01-01

The aim of this article was to show the effects of the electron radiation dose and presence of a compatibiliser on the peak melting temperature (T pm ) of the crystalline phase, crystallinity (X c ), and melt flow rate (MFR) of granulated blends of low-density polyethylene (LDPE), high-density polyethylene (HDPE), polypropylene (PP), polystyrene (PS), and polyethylene terephthalate (PET) as well as of blends of LDPE, HDPE, and PP. The purpose of applying the high-energy electron radiation with doses up to 300 kGy and of adding a compatibiliser was to enhance mechanical properties of the studied blends and, at the same time, to investigate the possibility of using this technique in the processes of recycling polymeric materials. As the compatibilisers, the styrene-ethylene/butylene-styrene elastomer grafted with maleic anhydride (SEBS-g-MA) and trimethylol propane trimethacrylate (TMPTA) were utilised; they were added at the amounts of 5, 10, and 15 wt% and 1, 2, and 3 wt%, respectively. The enhancement of mechanical properties was accompanied by the following effects, discussed in this article: (i) a decrease in the peak melting temperature upon the electron radiation for the crystalline phase of LDPE, HDPE, and PP that constituted the studied granulated blends and (ii) changes in MFR upon both the electron radiation and the addition of compatibilisers

PSD Applicability for Ashland Chemical's Maleic Anhydride Plant in Neal, West Virginia

Science.gov (United States)

This document may be of assistance in applying the New Source Review (NSR) air permitting regulations including the Prevention of Significant Deterioration (PSD) requirements. This document is part of the NSR Policy and Guidance Database. Some documents in the database are a scanned or retyped version of a paper photocopy of the original. Although we have taken considerable effort to quality assure the documents, some may contain typographical errors. Contact the office that issued the document if you need a copy of the original.

Molecular dynamics modeling the synthetic and biological polymers interactions pre-studied via docking

Science.gov (United States)

Tsvetkov, Vladimir B.; Serbin, Alexander V.

2014-06-01

In previous works we reported the design, synthesis and in vitro evaluations of synthetic anionic polymers modified by alicyclic pendant groups (hydrophobic anchors), as a novel class of inhibitors of the human immunodeficiency virus type 1 ( HIV-1) entry into human cells. Recently, these synthetic polymers interactions with key mediator of HIV-1 entry-fusion, the tri-helix core of the first heptad repeat regions [ HR1]3 of viral envelope protein gp41, were pre-studied via docking in terms of newly formulated algorithm for stepwise approximation from fragments of polymeric backbone and side-group models toward real polymeric chains. In the present article the docking results were verified under molecular dynamics ( MD) modeling. In contrast with limited capabilities of the docking, the MD allowed of using much more large models of the polymeric ligands, considering flexibility of both ligand and target simultaneously. Among the synthesized polymers the dinorbornen anchors containing alternating copolymers of maleic acid were selected as the most representative ligands (possessing the top anti-HIV activity in vitro in correlation with the highest binding energy in the docking). To verify the probability of binding of the polymers with the [HR1]3 in the sites defined via docking, various starting positions of polymer chains were tried. The MD simulations confirmed the main docking-predicted priority for binding sites, and possibilities for axial and belting modes of the ligands-target interactions. Some newly MD-discovered aspects of the ligand's backbone and anchor units dynamic cooperation in binding the viral target clarify mechanisms of the synthetic polymers anti-HIV activity and drug resistance prevention.

Copolymerization and terpolymerization of carbon dioxide/propylene oxide/phthalic anhydride using a (salenCo(III complex tethering four quaternary ammonium salts

Directory of Open Access Journals (Sweden)

Jong Yeob Jeon

2014-08-01

Full Text Available The (salenCo(III complex 1 tethering four quaternary ammonium salts, which is a highly active catalyst in CO2/epoxide copolymerizations, shows high activity for propylene oxide/phthalic anhydride (PO/PA copolymerizations and PO/CO2/PA terpolymerizations. In the PO/PA copolymerizations, full conversion of PA was achieved within 5 h, and strictly alternating copolymers of poly(1,2-propylene phthalates were afforded without any formation of ether linkages. In the PO/CO2/PA terpolymerizations, full conversion of PA was also achieved within 4 h. The resulting polymers were gradient poly(1,2-propylene carbonate-co-phthalates because of the drift in the PA concentration during the terpolymerization. Both polymerizations showed immortal polymerization character; therefore, the molecular weights were determined by the activity (g/mol-1 and the number of chain-growing sites per 1 [anions in 1 (5 + water (present as impurity + ethanol (deliberately fed], and the molecular weight distributions were narrow (Mw/Mn, 1.05–1.5. Because of the extremely high activity of 1, high-molecular-weight polymers were generated (Mn up to 170,000 and 350,000 for the PO/PA copolymerization and PO/CO2/PA terpolymerization, respectively. The terpolymers bearing a substantial number of PA units (fPA, 0.23 showed a higher glass-transition temperature (48 °C than the CO2/PO alternating copolymer (40 °C.

Formation and stability of Vitamin E enriched nanoemulsions stabilized by Octenyl Succinic Anhydride modified starch

Science.gov (United States)

Vitamin E (VE) is highly susceptible to autoxidation; therefore, it requires systems to encapsulate and protect it from autoxidation.In this study,we developed VE delivery systems, which were stabilized by Capsul® (MS), a starch modified with octenyl succinic anhydride. Influences of interfacial ten...

Polymer article of manufacture

Energy Technology Data Exchange (ETDEWEB)

Newlove, J.C.; McDougall, L.A.

1987-12-15

It is an object of this invention to provide an article and its use to enhance the production of hydrocarbons from geologial reservoirs, more particularly from fractured formations. It has been an additional object to devise a composition for providing controlled release of a reagent downhole, in a pipeline, in other oil-containing environments or fluids. It has been discovered that it is possible to provide for the introduction of an additive reagent into a liquid hydrocarbon by providing solid polymeric bodies each comprising a polymeric matrix containing a substantially water insoluble reagent such as a wax crystal modifier, demulsifier, scale inhibitor, corrosion inhibitor, biocide, ashless dispersant, antioxidant and mixtures thereof. These bodies are, in use, positioned at a location where it is desired to release the reagent into the substantially hydrocarbon fluid and, upon contact with fluid in this location, active reagent is released into the fluid. Thus in accordance with this invention there is provided a solid polymeric body comprising a polymer matrix containing a substantially water-insoluble reagent leachable into a substantially hydrocarbon liquid environment. The object of this invention has been realized in specific form by beads comprising a copolymeric matrix of methylmethacrylate and methacrylic acid containing the behenyl half ester of a C/sub 24/-C/sub 28/ alkenyl succinic anhydride polymer and having a diameter ranging from 0.2 to 1 mm. Such beads, when introduced downhole in a hydraulic fracturing operation, were found to inhibit paraffin wax deposition.

UV-Assisted 3D Printing of Glass and Carbon Fiber-Reinforced Dual-Cure Polymer Composites.

Science.gov (United States)

Invernizzi, Marta; Natale, Gabriele; Levi, Marinella; Turri, Stefano; Griffini, Gianmarco

2016-07-16

Glass (GFR) and carbon fiber-reinforced (CFR) dual-cure polymer composites fabricated by UV-assisted three-dimensional (UV-3D) printing are presented. The resin material combines an acrylic-based photocurable resin with a low temperature (140 °C) thermally-curable resin system based on bisphenol A diglycidyl ether as base component, an aliphatic anhydride (hexahydro-4-methylphthalic anhydride) as hardener and (2,4,6,-tris(dimethylaminomethyl)phenol) as catalyst. A thorough rheological characterization of these formulations allowed us to define their 3D printability window. UV-3D printed macrostructures were successfully demonstrated, giving a clear indication of their potential use in real-life structural applications. Differential scanning calorimetry and dynamic mechanical analysis highlighted the good thermal stability and mechanical properties of the printed parts. In addition, uniaxial tensile tests were used to assess the fiber reinforcing effect on the UV-3D printed objects. Finally, an initial study was conducted on the use of a sizing treatment on carbon fibers to improve the fiber/matrix interfacial adhesion, giving preliminary indications on the potential of this approach to improve the mechanical properties of the 3D printed CFR components.

UV-Assisted 3D Printing of Glass and Carbon Fiber-Reinforced Dual-Cure Polymer Composites

Directory of Open Access Journals (Sweden)

Marta Invernizzi

2016-07-01

Full Text Available Glass (GFR and carbon fiber-reinforced (CFR dual-cure polymer composites fabricated by UV-assisted three-dimensional (UV-3D printing are presented. The resin material combines an acrylic-based photocurable resin with a low temperature (140 °C thermally-curable resin system based on bisphenol A diglycidyl ether as base component, an aliphatic anhydride (hexahydro-4-methylphthalic anhydride as hardener and (2,4,6,-tris(dimethylaminomethylphenol as catalyst. A thorough rheological characterization of these formulations allowed us to define their 3D printability window. UV-3D printed macrostructures were successfully demonstrated, giving a clear indication of their potential use in real-life structural applications. Differential scanning calorimetry and dynamic mechanical analysis highlighted the good thermal stability and mechanical properties of the printed parts. In addition, uniaxial tensile tests were used to assess the fiber reinforcing effect on the UV-3D printed objects. Finally, an initial study was conducted on the use of a sizing treatment on carbon fibers to improve the fiber/matrix interfacial adhesion, giving preliminary indications on the potential of this approach to improve the mechanical properties of the 3D printed CFR components.

Efficient photochemical generation of peroxycarboxylic nitric anhydrides with ultraviolet light emitting diodes

Science.gov (United States)

Rider, N. D.; Taha, Y. M.; Odame-Ankrah, C. A.; Huo, J. A.; Tokarek, T. W.; Cairns, E.; Moussa, S. G.; Liggio, J.; Osthoff, H. D.

2015-01-01

Photochemical sources of peroxycarboxylic nitric anhydrides (PANs) are utilized in many atmospheric measurement techniques for calibration or to deliver an internal standard. Conventionally, such sources rely on phosphor-coated low-pressure mercury (Hg) lamps to generate the UV light necessary to photo-dissociate a dialkyl ketone (usually acetone) in the presence of a calibrated amount of nitric oxide (NO) and oxygen (O2). In this manuscript, a photochemical PAN source in which the Hg lamp has been replaced by arrays of ultraviolet light-emitting diodes (UV-LEDs) is described. The output of the UV-LED source was analyzed by gas chromatography (PAN-GC) and thermal dissociation cavity ring-down spectroscopy (TD-CRDS). Using acetone, diethyl ketone (DIEK), diisopropyl ketone (DIPK), or di-n-propyl ketone (DNPK), respectively, the source produces peroxyacetic (PAN), peroxypropionic (PPN), peroxyisobutanoic (PiBN), or peroxy-n-butanoic nitric anhydride (PnBN) from NO in high yield (> 90%). Box model simulations with a subset of the Master Chemical Mechanism (MCM) were carried out to rationalize products yields and to identify side products. The use of UV-LED arrays offers many advantages over conventional Hg lamp setups, including greater light output over a narrower wavelength range, lower power consumption, and minimal generation of heat.

Directory of Open Access Journals (Sweden)

Kamal M. El-Gamal

2016-12-01

Full Text Available A series of 3-substituted 6-methoxy-1H-pyrazolo [3,4-b]quinoline derivatives was synthesized by treating 6-methoxy-1H-pyrazolo[3,4-b]quinolin-3-amine (6 with different acid anhydrides including succinic anhydride, maleic anhydride and phthalic anhydride. Also, a series of 3-heteroaryl-2-chloro-6-methoxyquinolines was prepared through 1,3-dipolar cycloaddition of different bi-nucleophiles including hydrazine hydrate, hydroxylamine hydrochloride, thiourea, guanidine hydrochloride, urea and metformin hydrochloride to the chalcone derivative 3-(2-chloro-6-methoxyquinolin-3-yl-1-(4-methoxyphenylprop-2-en-1-one. Structural identifications of all products were reported and the new compounds were screened for their in vitro antimicrobial activity against Streptococcus pneumonia and Bacillus subtilis as examples for Gram-positive bacteria, Pseudomonas aeruginosa and Escherichia coli as examples for Gram-negative bacteria, and Aspergillus fumigatus, Syncephalastrum racemosum, Geotriucum candidum and Candida albicans as representative examples of fungi. The majority of tested compounds showed moderate activities against a wide range of the selected organisms. Among the tested compounds, pyrimidine derivatives 16 and 17 showed the highest antimicrobial activity against gram-positive strains while the highest activity against E. coli as example for Gram-negative strains was observed in the case of 11 and 17. Compounds 14 and 17 were found to be extremely potent against three of the selected fungal strains.

Preliminary characterization in the development of the nano composite low density polyethylene with attapulgite clay

International Nuclear Information System (INIS)

Domingos, Luanda G.; Rego, Jose K.M.A. do; Ito, Edson N.; Acchar, Wilson

2011-01-01

The aim of this study was a preliminary study of the physical, thermal and rheological properties of the materials to be used in the development of nano composite low density polyethylene (LDPE) with Brazilian attapulgite clay (ATP), with and without the use of a compatibilizing agent interfacial, polyethylene grafted with maleic anhydride (PE-g-MAH). The materials were characterized by X-ray diffraction (XRD), thermogravimetry (TG) and torque rheometry. The materials were characterized and potentially could be developed polymeric nano composites with technological applications using attapulgite fibers in the nanometer scale. (author)

Aspects and prospects of the chemistry of organic heterocycles (review)

International Nuclear Information System (INIS)

Schroth, W.

1986-01-01

The systematics of heterocycles, their place in organic chemistry, and their significance for theory and practice are discussed. Problems of the chemistry of heterocycles are discussed on the examples of systems with various types of conjugation and ring sizes. The focus is on the principles of synthesis of heterocycles, in particular, those based on acetylene, various C 3 fragments, carbon disulfide, and maleic anhydride. Individual sections of the survey are devoted to the role of heterocycles in biosynthesis, as well as certain problems common to the chemistry of heterocycles, biochemistry, and macromolecular chemistry

Synthesis and Characterization of a New Heterocyclic Azo Pigment

International Nuclear Information System (INIS)

Asniza, M.; Issam, A.M.; Khalil, H.P.S.A.

2011-01-01

A new heterocyclic coupling agent has been produced from the reaction of maleic anhydride and p-aminophenol, namely N-(4-hexahydrophenol)maleimide. The coupling agent underwent azo coupling reaction with aromatic amine, which is p-aminophenol to produce a new heterocyclic azo pigment. The pigment was then subjected to solubility, hiding power and light fastness test. Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet/ Visible (UV/Vis) Spectroscopy, and Nuclear Magnetic Resonance Spectroscopy ( 1 H-NMR, 13 C-NMR) were used to obtain the characteristics and structural features of the pigment. (author)

Effects of Organomontmorillonite Content on Morphology and Mechanical and Thermal Properties of Poly(2,6-dimethyl-1,4-phenylene oxide/Polyamide-66 Nanocomposites

Directory of Open Access Journals (Sweden)

Kunxiao Yang

2016-01-01

Full Text Available The nanocomposites consisting of polymer matrix and nanofiller have attracted great attention because of the improved physical properties. In this paper, organomontmorillonite (OMMT was introduced into poly(2,6-dimethyl-1,4-phenylene oxide grafted maleic anhydride (PPO-g-MA compatibilized poly(2,6-dimethyl-1,4-phenylene oxide/polyamide-66 (PPO/PA66 blends by melt extrusion. The morphology of PPO/PA66 nanocomposites with different amounts of OMMT was investigated using transmission electron microscopy (TEM, wide-angle X-ray diffraction (WAXD, and scanning electron microscopy (SEM. The OMMT platelets exhibited an exfoliated structure in the PA66 matrix and an intercalated structure on the surface of PPO domains at low OMMT loading (2 phr. However, the exfoliated platelets in matrix were found to transform into intercalated stacks by adding 6 phr of OMMT. The mechanical properties and thermal stability were significantly improved with the coexistence of exfoliated and intercalated OMMT at low OMMT loading (2–4 phr. The exfoliated OMMT platelets imposed a confinement effect on the macromolecular chains and thereby increased the storage modulus and complex viscosity of nanocomposites.

Mechanical properties, morphology and thermal degradation of a biocomposite of polypropylene and curaua fibers: coupling agent effect

Directory of Open Access Journals (Sweden)

Barbara Mano

2013-01-01

Full Text Available Biocomposites of polymers with vegetal fibers have a broad spectrum of applications due to their high specific properties in comparison to their counterparts made with fiberglass. Polypropylene, PP, composites with curaua fiber compatibilized with different concentrations of maleic anhydride grafted polypropylene, PP-g-MA, were characterized according to their mechanical properties, morphologies and thermal stabilities in oxidative and inert atmospheres. The composites were prepared by single screw extrusion and injection molded specimens were used for testing. The composite with 20 wt % of curaua fiber with and without compatibilizer presented improved mechanical properties compared to pure PP. The use of PP-g-MA as a compatibilizer significantly increased fiber/matrix adhesion, however, the mechanical properties were only slightly improved in comparison with composites without compatibilizer. We observed an improvement in thermal stability of the composites, compared to that expected from the weighted average of the individual components, both under inert and oxidative atmospheres. Furthermore, the thermal stability improved under inert atmosphere as a function of the concentration of compatibilizer. In this situation, indeed, there was a different shift of the weight loss processes owing to the presence of the compatibilizer.

Effect of carboxylic acids as compatibilizer agent on mechanical properties of thermoplastic starch and polypropylene blends.

Science.gov (United States)

Martins, Andréa Bercini; Santana, Ruth Marlene Campomanes

2016-01-01

In this work, polypropylene/thermoplastic starch (PP/TPS) blends were prepared as an alternative material to use in disposable packaging, reducing the negative polymeric environmental impact. Unfortunately, this material displays morphological characteristics typical of immiscible polymer blends and a compatibilizer agent is needed. Three different carboxyl acids: myristic (C14), palmitic (C16) and stearic acids (C18) were used as natural compatibilizer agent (NCA). The effects of NCA on the mechanical, physical, thermal and morphological properties of PP/TPS blends were investigated and compared against PP/TPS with and without PP-grafted maleic anhydride (PPgMA). When compared to PP/TPS, blends with C18, PPgMA and C14 presented an improvement of 25, 22 and 17% in tensile strength at break and of 180, 194 and 259% in elongation at break, respectively. The highest increase, 54%, in the impact strength was achieved with C14 incorporation. Improvements could be seen, through scanning electron microscopy (SEM) images, in the compatibility between the immiscible components by acids incorporation. These results showed that carboxylic acids, specifically C14, could be used as compatibilizer agent and could substitute PPgMA. Copyright © 2015 Elsevier Ltd. All rights reserved.

Bio-composites fabricated by sandwiching sisal fibers with polypropylene (PP)

Energy Technology Data Exchange (ETDEWEB)

Sosiati, H., E-mail: hsosiati@gmail.com [Nanomaterials Research Group, LPPT Universitas Gadjah Mada (Indonesia); Nahyudin, A., E-mail: ahmadnahyudin@yahoo.co.id; Fauzi, I., E-mail: ikhsannurfauzi@gmail.com; Wijayanti, D. A., E-mail: wijayantidwiastuti@gmail.com [Department of Physics, Faculty of Mathematics and Natural Sciences, Gadjah Mada University (Indonesia); Triyana, K., E-mail: triyana@ugm.ac.id [Nanomaterials Research Group, LPPT Universitas Gadjah Mada (Indonesia); Department of Physics, Faculty of Mathematics and Natural Sciences, Gadjah Mada University (Indonesia)

2016-04-19

Sisal fibers reinforced polypropylene (PP) composites were successfully fabricated using sandwiching sisal fibers with PP sheets. The ratio of fiber and polymer matrix was 50:50 (wt. %). Untreated short and long sisal fibers, and alkali treated short sisal fibers in 6% NaOH at 100°C for 1 and 3 h were used as reinforcement or fillers. A small amount (3 wt. %) of maleic anhydride grafted polypropylene (MAPP) was added as a coupling agent. Scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy were used to characterize the surface morphology and chemical composition of the fibers, respectively. Flexural test of sisal/PP composites was done according to ASTM D 790-02. The results showed that flexural strength of untreated long fiber reinforced composite is much higher than that of the untreated and alkali treated short fibers reinforced composites with and without the addition of MAPP. Alkalization related to fiber surface modification, fiber length/fiber orientation and a composite fabrication technique are important factors in contributing to the fiber distribution within the matrix, the bonding between the fiber and the matrix and the enhancement of flexural strength of the bio-composite.

Modelling the size and polydispersity of magnetic hybrid nanoparticles for luminescent sensing of oxygen

International Nuclear Information System (INIS)

Marín-Suárez, Marta; Arias-Martos, María C.; Fernández-Sánchez, Jorge F.; Fernández-Gutiérrez, Alberto; Galeano-Díaz, Teresa

2013-01-01

We report on a strategy to model both the size (d) and the polydispersity (PdI) of magnetic oxygen-sensitive nanoparticles with a typical size of 200 nm in order to increase the surface area. The strategy is based on experimental design and Response Surface Methodology. Nanoparticles were prepared by mini emulsion solvent evaporation of solutions of poly(styrene-co-maleic anhydride). Features of this strategy include (1) a quick selection of the most important variables that govern d and PdI; (2) a better understanding of the parameters that affect the performance of the polymer; and (3) optimized conditions for the synthesis of nanoparticles of targeted d and PdI. The results were used to produce nanoparticles in sizes that range from 100 to 300 nm and with small polydispersity. The addition of a platinum porphyrin complex that acts as a luminescent probe for oxygen and of magnetite (Fe 3 O 4 ) to the polymeric particles, did not affect d and PdI, thus demonstrating that this strategy simplifies their synthesis. The resulting luminescent and magnetic sensor nanoparticles respond to dissolved oxygen with sensitivity (Stern-Volmer constant) of around 35 bar −1 . (author)

Bio-composites fabricated by sandwiching sisal fibers with polypropylene (PP)

International Nuclear Information System (INIS)

Sosiati, H.; Nahyudin, A.; Fauzi, I.; Wijayanti, D. A.; Triyana, K.

2016-01-01

Sisal fibers reinforced polypropylene (PP) composites were successfully fabricated using sandwiching sisal fibers with PP sheets. The ratio of fiber and polymer matrix was 50:50 (wt. %). Untreated short and long sisal fibers, and alkali treated short sisal fibers in 6% NaOH at 100°C for 1 and 3 h were used as reinforcement or fillers. A small amount (3 wt. %) of maleic anhydride grafted polypropylene (MAPP) was added as a coupling agent. Scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy were used to characterize the surface morphology and chemical composition of the fibers, respectively. Flexural test of sisal/PP composites was done according to ASTM D 790-02. The results showed that flexural strength of untreated long fiber reinforced composite is much higher than that of the untreated and alkali treated short fibers reinforced composites with and without the addition of MAPP. Alkalization related to fiber surface modification, fiber length/fiber orientation and a composite fabrication technique are important factors in contributing to the fiber distribution within the matrix, the bonding between the fiber and the matrix and the enhancement of flexural strength of the bio-composite.

Bio-composites fabricated by sandwiching sisal fibers with polypropylene (PP)

Science.gov (United States)

Sosiati, H.; Nahyudin, A.; Fauzi, I.; Wijayanti, D. A.; Triyana, K.

2016-04-01

Sisal fibers reinforced polypropylene (PP) composites were successfully fabricated using sandwiching sisal fibers with PP sheets. The ratio of fiber and polymer matrix was 50:50 (wt. %). Untreated short and long sisal fibers, and alkali treated short sisal fibers in 6% NaOH at 100°C for 1 and 3 h were used as reinforcement or fillers. A small amount (3 wt. %) of maleic anhydride grafted polypropylene (MAPP) was added as a coupling agent. Scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy were used to characterize the surface morphology and chemical composition of the fibers, respectively. Flexural test of sisal/PP composites was done according to ASTM D 790-02. The results showed that flexural strength of untreated long fiber reinforced composite is much higher than that of the untreated and alkali treated short fibers reinforced composites with and without the addition of MAPP. Alkalization related to fiber surface modification, fiber length/fiber orientation and a composite fabrication technique are important factors in contributing to the fiber distribution within the matrix, the bonding between the fiber and the matrix and the enhancement of flexural strength of the bio-composite.

Highly Efficient Fumed Silica Nanoparticles for Peptide Bond Formation: Converting Alanine to Alanine Anhydride.

Science.gov (United States)

Guo, Chengchen; Jordan, Jacob S; Yarger, Jeffery L; Holland, Gregory P

2017-05-24

In this work, thermal condensation of alanine adsorbed on fumed silica nanoparticles is investigated using thermal analysis and multiple spectroscopic techniques, including infrared (IR), Raman, and nuclear magnetic resonance (NMR) spectroscopies. Thermal analysis shows that adsorbed alanine can undergo thermal condensation, forming peptide bonds within a short time period and at a lower temperature (∼170 °C) on fumed silica nanoparticle surfaces than that in bulk (∼210 °C). Spectroscopic results further show that alanine is converted to alanine anhydride with a yield of 98.8% during thermal condensation. After comparing peptide formation on solution-derived colloidal silica nanoparticles, it is found that fumed silica nanoparticles show much better efficiency and selectivity than solution-derived colloidal silica nanoparticles for synthesizing alanine anhydride. Furthermore, Raman spectroscopy provides evidence that the high efficiency for fumed silica nanoparticles is likely related to their unique surface features: the intrinsic high population of strained ring structures present at the surface. This work indicates the great potential of fumed silica nanoparticles in synthesizing peptides with high efficiency and selectivity.

Perylene anhydride fused porphyrins as near-infrared sensitizers for dye-sensitized solar cells

KAUST Repository

Jiao, Chongjun

2011-07-15

Two perylene anhydride fused porphyrins 1 and 2 have been synthesized and employed successfully in dye-sensitized solar cells (DSCs). Both compounds showed broad incident monochromatic photon-to-current conversion efficiency spectra covering the entire visible spectral region and even extending into the near-infrared (NIR) region up to 1000 nm, which is impressive for ruthenium-free dyes in DSCs. © 2011 American Chemical Society.

Simultaneous determination of furfural and its degradation products, furoic acid and maleic acid, in transformer oil by the reversed-phase vortex-assisted liquid-liquid microextraction followed by high-performance liquid chromatography.

Science.gov (United States)

Wang, Yifan; Li, Haiyan; Yang, Zhen; Zhang, Weijie; Hua, Jia

2017-12-01

To explore why the use of furfural as a transformer oil-paper insulation aging characteristic is problematic in real world application, we developed a method for the simultaneous determination of furfural, furoic acid, and maleic acid in transformer oil by reversed-phase vortex-assisted liquid-liquid microextraction combined with high-performance liquid chromatography. The conditions for the proposed method were optimized, and the obtained extract can be directly analyzed by high-performance liquid chromatography. The detection limits (signal-to-noise ratio = 3) of the method ranged from 1.0 to 4.6 μg/L, the enrichment factors for furfural, furoic acid, maleic acid, and fumaric acid were 4.6, 25.1, 15.6, and 17.5, respectively, and the recovery rates for three analytes (fumaric acid was undetected) range from 82.1 to 106.2%. The contents of furfural, furoic acid, and maleic acid resulted from accelerated aging of transformer insulation oil-paper were measured using the present method for the first time, and the aging samples were analyzed by liquid chromatography with mass spectrometry for the identification of furoic acid and maleic acid in the aging transformer oil samples. Using the optimal method, the target products of samples at different aging time were tracked and measured. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Anodic incineration of phthalic anhydride using RuO2–IrO2–SnO2–TiO2 coated on Ti anode

Directory of Open Access Journals (Sweden)

S. Chellammal

2016-11-01

Full Text Available Phthalic anhydride is a toxic and non-biodegradable organic compound and is widely used for the production of dyes. This paper has investigated the electrochemical oxidation of phthalic anhydride in an undivided cell at different experimental parameters such as pH, current density and supporting electrolytes on the anode of titanium substrate coated with mixed metal oxides of RuO2, IrO2, SnO2 and TiO2 prepared by thermal decomposition method. The surface morphology and the structure of the above anode were characterized by scanning electron microscopy, electron dispersion microscopy and X-ray diffraction. The study shows that the electrode exhibits good electro catalytic activity together with chemical stability during the treatment of the phthalic anhydride. At pH 3, the maximum removal of COD of 88% with energy consumption of 30.5 kW h kg−1 was achieved by the addition of 10 g l−1 NaCl in 0.2 mol dm−3 Na2SO4 at 5 Adm−2. This electrolytic investigation offers an attractive alternative method for the destruction of industrial effluents contaminated with phthalic anhydride.

Enzymatic modification of natural and synthetic polymers using lipases and proteases

Science.gov (United States)

Chakraborty, Soma

Enzymatic modification of natural/synthetic polymers [starch nanoparticles, poly (n-alkyl acrylates) and poly(vinyl formamide)] was studied. Enzymes used for catalysis were lipases and proteases. Starch nanoparticles (40nm diameter) were incorporated into AOT-coated reverse micelles. Reactions performed with the acylating agents vinyl stearate, epsilon-caprolactone and maleic anhydride in toluene in presence of Novozyme-435 at 40°C for 36h gave products with degrees of substitution of 0.8, 0.6 and 0.4 respectively. DEPT-135 NMR spectra revealed that the modification occurred regioselectively at the C-6 position of the glucose units. Infrared microspectroscopy showed that the surfactant coated starch nanoparticles diffuse into pores of Novozyme-435 beads, coming in close proximity with CALB to promote modification. The modified products retained nanoscale dimensions. Catalysis of amide bond formation between a low molar mass amine and ester side groups of poly(n-alkyl acrylates)[poly(ethyl acrylate), poly(methyl acrylate) and poly(butyl acrylate)] was also examined. The nucleophiles were mono and diamines. Among the poly(n-alkyl acrylates) and the lipases studied, poly(ethyl acrylate) was the preferred substrate and Novozyme-435 the most active lipase. Poly(ethyl acrylate) in 80% by-volume toluene was reacted with 1 equivalent per repeat unit of hexyl amine at 70°C in presence of Novozyme-435. The product contained 10.6 mol% amide groups. Attempts to increase the amidation beyond 10--11 mol% by increasing the reaction time or use of fresh enzyme were unsuccessful, showing that poly(ethylacrylate-co-10mol%hexylacrylamide) is a poor substrate for further acylation. When chiral amines ([R,S]-alpha-methyl benzylamine, [R,S]-beta-methyl phenyl amine) were used as nucleophiles, Novozyme-435 enantioselectively catalyzed amidation of poly(ethyl acrylate). Poly(vinyl formamide), P(VfAm) by acid or base-catalyzed hydrolysis leads to poly(vinylamine), P(VAm), and

The hidden radiation chemistry in plasma modification and XPS analysis of polymer surfaces

International Nuclear Information System (INIS)

George, G.A.; Le, T.T.; Elms, F.M.; Wood, B.J.

1996-01-01

Full text: The surface modification of polymers using plasma treatments is being widely researched to achieve changes in the surface energetics and consequent wetting and reactivity for a range of applications. These include i) adhesion for polymer bonding and composite material fabrication and ii) biocompatibility of polymers when used as orthopedic implants, catheters and prosthetics. A low pressure rf plasma produces a variety of species from the introduced gas which may react with the surface of a hydrocarbon polymer, such as polyethylene. In the case of 0 2 and H 2 0, these species include oxygen atoms, singlet molecular oxygen and hydroxyl radicals, all of which may oxidise and, depending on their energy, ablate the polymer surface. In order to better understand the reactive species formed both in and downstream from a plasma and the relative contributions of oxidation and ablation, self-assembled monolayers of n-alkane thiols on gold are being used as well characterised substrates for quantitative X-ray photoelectron spectroscopy (XPS). The identification and quantification of oxidised carbon species on plasma treated polymers from broad, asymmetric XPS signals is difficult, so derivatisation is often used to enhance sensitivity and specificity. For example, trifluoroacetic anhydride (TFAA) selectively labels hydroxyl functionality. The surface analysis of a modified polymer surface may be confounded by high energy radiation chemistry which may occur during XPS analysis. Examples include scission of carbon-halogen bonds (as in TFM adducts), decarboxylation and main-chain polyene formation. The extent of free-radical chemistry occurring in polyethylene while undergoing XPS analysis may be seen by both ESR and FT-IR analysis

Evaluation of genotoxic activity of maleic hydrazide, ethyl methane sulfonate, and N-nitroso diethylamine in Tradescantia

OpenAIRE

Alvarez-Moya Carlos; Santerre-Lucas Anne; Zúñiga-González Guillermo; Torres-Bugarín Olivia; Padilla-Camberos Eduardo; Feria-Velasco Alfredo

2001-01-01

Objective. To assess the genotoxic activity of N-nitroso diethylamine (NDEA), maleic hydrazide (MH), and ethyl methane sulfonate (EMS) using two systems: the comet assay on nuclei from Tradescantia, and the pink mutation test on Tradescantia staminal hairs (clone 4430). Material and Methods. Tradescantia cups was obtained from Laboratorio de Citogenética y Mutagénesis del Centro de Ciencias de la Atmósfera de la Universidad Nacional Autónoma de México and treated with: N-nitroso diethylamine ...

Process for producing a polymer

Energy Technology Data Exchange (ETDEWEB)

Koshimura, M; Haruta, K; Matsuzaka, J; Terakado, H

1969-02-13

A novel polymer is produced by a novel polymerization or copolymerization process in the presence of a free radical-forming catalyst or radical-forming irradiation energy to provide a monomer of the general formula CH/sub 2/=C(R/sub 1/)(COO)-(R/sub 2/OOCR/sub 3/COO)sub(n)-R/sub 2/OH wherein R/sub 1/ is hydrogen, halogen or alkyl radical containing one or two atoms; R/sub 2/ is an epoxy compound residue; R/sub 3/ is a polybasic anhydride residue; and n is an integer. This polymer: (1) enables the cross-linking reaction, (2) improves the adhesiveness of adhesives, pigments, films and coatings; (3) is adjustable for mutual solubility and affinity when blending with other solvents and resins; (4) is resistant to yellowing and mechanically stronger than the benzene nucleus of styrene; (5) improves the textile dyeing affinity, adhesiveness and dispersion of pigments, and the dimensional stability of films and sheets; (6) is suitable as a molding material of synthetic resins, adhesives and coatings because of its three dimensional cross-linking construction; (7) can control the hardness, flexibility and rigidity of the molding materials; and (8) can lower the cost of production. In an example, 10 g of the monomer of the above mentioned formula wherein n=1, R/sub 1/=CH/sub 3/, R/sub 2/=-(CH/sub 2/)/sub 2/ and R/sub 3/ is ortho-substituted benzene, and 0.1 g of benzol peroxide, are added to ampoule, sealed and polymerized at 120/sup 0/C for 2 hours. Next the contents are precipitated in a large amount of benzene to produce a polymer having a molecular weight of 9,500. The products have good dimensional stability as molding materials.

Investigation of photo-biodegradation of starch-filled polyethylene films under the environment conditions of Tehran

International Nuclear Information System (INIS)

Naeimian, F.; Khoylou, F.; Sheikh, N.; Akhavan, A.; Hassanpour, S.; Sohrabpour, M.

2006-01-01

In this work biodegradable polymers have been formulated for packaging purposes and with a view to reduce the environmental accumulation of plastic waste. Degradation of the polymers under the specific weathering conditions of Tehran was studied. In this work low-density polyethylene was formulated with two wheat starch concentrations, maleic anhydride, glycerol as well as a pro-oxidant system of oleic acid, benzoyl peroxide and ferric stearate. The formulated master batches were mixed by using a laboratory two-roll mill at 190 d ig C prepared master batches were mixed with the commercial low-density polyethylene to prepare compounds 1 and 2 containing 1.2 and 6.4 percents wheat starch. The low-density polyethylene control films as well as the formulated compounds were compression moulded in a hot press at 130 d ig C films were subjected to three general conditions of atmospheric exposure, buried in soil and combined conditions of soil burial/ atmospheric exposure. The three environmental conditions impact upon the formulated and control films were investigated through tensile strength, elongation-at-break, carbonyl index, water absorption, weight loss as well as SEM analysis. The microbial investigation was followed by growing the Penicillium Asymmetrica, which had the main population in microbial flora of the soil, on formulated and control films. The studies revealed that the incorporation of this pro-oxidant system with the addition of 6.4% wheat starch enhance the degradation rate of commercial low-density polyethylene films to a significant degree

Comparative study of modified polypropylene nanocomposites under environment and accelerated ageing conditions

International Nuclear Information System (INIS)

Komatsu, Luiz Gustavo Hiroki

2016-01-01

The understanding of degradation mechanism action on the polymer nanocomposites in face of weathering (UV light, heat, acid rain, among others), is the key for development of new additives and new applications. In this work the nanocomposite synthesis was carried in molten state, using twin-screw extruder. The polymer matrix was the HMS-PP (high melt polypropylene) synthesized by gamma irradiation and the nanometric inorganic component was the montmorillonite clay. For better compatibilization between the matrix and clay, it were used maleic anhydride as coupling agent. For environment and in oven accelerated aging assays, the dumbbell samples were prepared under hot pressing. The characterization of clay addition effects and aging effects on the nanocomposites, required the use of techniques of Differential Scanning Calorimetry (DSC), Thermogravimetry (TGA), Fourier Transformed Infrared Spectroscopy (FT-IR), Xray Fluorescence (WDXRF), Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS) and mechanical properties. Samples with 0.1; 1; 3; 5; 10 % of clay were tested. The sample with 5% of clay showed better stability on the environmental assay and accelerated aging in oven assay. On the other hand, the sample with higher percent of clay (10%), was more degraded under on environmental aging than under accelerated aging in stove. In this case, became more resistant until 56 days of assay. On the studied concentrations (less than ≤ 3%) of clay, it can be seen an equilibrium between barrier effect and metallic ions action accelerating the degradative process. (author)

Preparation and characterization of an aromatic polyester/polyaniline composite and its improved counterpart

Directory of Open Access Journals (Sweden)

C. S. Wu

2012-06-01

Full Text Available Poly(butylene terephthalate (PBT composites containing polyaniline (PANI were prepared using a melt-blending process. Maleic anhydride-grafted PBT (PBT-g-MA and PANI were used to improve the compatibility of PANI within the PBT matrix. PBT-g-MA/PANI composites exhibited noticeably superior mechanical properties compared with those of PBT/PANI due to greater compatibility with the added PANI. The antibacterial and antistatic properties of the composites were also evaluated. Escherichia coli were chosen as the standard bacteria for determining the antibacterial properties of the composite materials. The PBT-g-MA/PANI composites showed markedly enhanced antibacterial and antistatic properties compared to PBT/PANI composites due to the formation of imide bonds from condensation of the anhydride carboxyl acid groups of PBT-g-MA with the amino groups of PANI. The optimal level of PANI in the composites was 9 wt%, as excess PANI led to separation of the two organic phases, lowering their compatibility.

Catalytic ring-​opening copolymerization of limonene oxide and phthalic anhydride : toward partially renewable polyesters

NARCIS (Netherlands)

Hosseini Nejad, E.; Pionasari, A; Melis, van C.G.W.; Koning, C.E.; Duchateau, R.

2013-01-01

Catalytic ring-¿opening copolymn. of limonene oxide with phthalic anhydride was performed applying metal t-¿Bu-¿salophen complexes (t-¿Bu-¿salophen)¿MX; M = Cr, X = Cl (1)¿, M = Al, X = Cl (2)¿, M = Co, X = OAc (3)¿, M = Mn, X = Cl (4)¿, t-¿Bu-¿salophen =

Modified Julia Olefination on Anhydrides: Extension and Limitations. Application to the Synthesis of Maculalactone B.

Science.gov (United States)

Dussart, Nicolas; Trinh, Huu Vinh; Gueyrard, David

2016-10-07

The preparation of exo-enol esters from cyclic anhydrides is reported using a modified Julia olefination. The reaction is highly stereoselective. The Smiles rearrangement can be performed in a one-pot process, giving a straightforward access to exo-enol lactones. Furthermore, the reaction was extended to semistabilized sulfones, and this methodology was applied to the synthesis of maculalactone B.

The influence of a residual group in low-molecular-weight allergoids of Artemisia vulgaris pollen on their allergenicity, IgE- and IgG-binding properties.

Science.gov (United States)

Cirković, T; Gavrović-Jankulović, M; Prisić, S; Jankov, R M; Burazer, L; Vucković, O; Sporcić, Z; Paranos, S

2002-11-01

Reaction of epsilon-amino groups of lysine with potassium cyanate, maleic, or succinic anhydride leads to allergoids of low molecular weight. No study has been performed to compare their properties and investigate the influence of a residual group on allergenicity and human IgE- and IgG-binding of these derivatives. Allergoids of a pollen extract of Artemisia vulgaris were obtained by means of potassium cyanate, and succinic and maleic anhydride. Biochemical properties were investigated by determination of amino groups, enzyme activity, isoelectric focusing IEF and SDS-PAGE. IgE- and IgG-binding was determined using immunoblots and ELISA inhibition. Allergenicity was investigated by skin prick tests (SPT) on a group of 52 patients, of which 6 were control subjects, 30 were patients with no previous immunotherapy (IT), and 16 were patients undergoing immunotherapy. The same degree of amino-group modification (more than 85%), residual enzyme activity (less then 15%), IEF, and SDS-PAGE pattern were noted. In the immunoblots of IgE-binding, there was more pronounced reduction in the succinyl and maleyl derivatives than in the carbamyl one. IgG-binding was less affected by carbamylation than by acid anhydride modification. The SPT showed that the succinylated derivative had the most reduced allergenicity (98% showed a reduced wheal diameter when tested with the succinyl derivative, 87% with the maleyl allergoid, and 83% with the carbamyl allergoid). The most significant difference among allergoids could be seen in the group of patients with high skin reactivity (83% of patients showed no reaction to the succinyl derivative when compared to the value of 28% for the carbamyl derivative or 22% for the maleyl derivative). According to our results, all three modification procedures yielded allergoids with a similar extent of modification. No single biochemical parameter investigated in the study could predict the degree of reduced allergenicity in vivo. The most reduced

Preparation of epoxy/zirconia hybrid materials via in situ polymerization using zirconium alkoxide coordinated with acid anhydride

International Nuclear Information System (INIS)

Ochi, Mitsukazu; Nii, Daisuke; Harada, Miyuki

2011-01-01

Highlights: → Novel epoxy/zirconia hybrid materials were synthesized via in situ polymerization using zirconium alkoxide coordinated with acid anhydride. → The half-ester compound of acid anhydride desorbed from zirconium played as curing agent of epoxy resin. → The zirconia was uniformly dispersed in the epoxy matrix on the nanometer or sub-nanometer scale by synchronizing the epoxy curing and sol-gel reactions. → The refractive indices of the hybrid materials significantly improved with an increase in the zirconia content. - Abstract: Novel epoxy/zirconia hybrid materials were synthesized using a bisphenol A epoxy resin (diglycidyl ether of bisphenol A; DGEBA), zirconium(IV)-n-propoxide (ZTNP), and hexahydrophthalic anhydride (HHPA) via in situ polymerization. HHPA played two roles in this system: it acted as a modifier to control the hydrolysis and condensation reactions of zirconium alkoxide and also as a curing agent - the half-ester compound of HHPA desorbed from zirconium reacted with the epoxy resin to form the epoxy network. As a result, both the sol-gel reaction and epoxy curing occurred simultaneously in a homogeneous solution, and organic-inorganic hybrid materials were readily obtained. Further, the zirconia produced by the in situ polymerization was uniformly dispersed in the epoxy matrix on the nanometer or sub-nanometer scale; thus, hybrid materials that exhibited excellent optical transparency were obtained. Furthermore, the heat resistance of the hybrid materials could be improved by hybridization with zirconia. And, the refractive indices of the hybrid materials significantly improved with an increase in the zirconia content.

Synthesis and characterization of radiation grafted films for removal of arsenic and some heavy metals from contaminated water

International Nuclear Information System (INIS)

Chowdhury, M.N.K.; Khan, M.W.; Mina, M.F.; Beg, M.D.H.; Khan, Maksudur R.; Alam, A.K.M.M.

2012-01-01

Grafting of styrene/maleic anhydride and methyl methacrylate/maleic anhydride binary monomers onto the low density polyethylene film was performed using the γ-ray irradiation technique. Then, the synthesized grafted films were treated with different ammonia derivatives for developing chelating functionalization. These chelating products were characterized by the gravimetric method as well as by the Fourier transformed infrared spectroscopic method, and were used for removal of arsenic and some heavy metals from aqueous solutions. The optimum absorbed dose of 30 kGy reveals the graft yielding of about 325% in the films. Uptake of arsenic and some heavy-metal ions (Cr(III), Mn(II), Fe(III), Ni(II), Cu(II) and Pb(II)) from contaminated water by the chelating functionalized films (CFF) was examined by an atomic absorption spectrophotometer. The maximum arsenic removal capacity of 5062 mg/kg has been observed for the film treated with hydroxylamine hydrochloride. The CFF prepared by semicarbazide and thiol analogs show affinity toward the metal ions with an order: Cu(II)>Fe(III)>Mn(II) etc. The results obtained from this study indicate that the functionalized films show good chelating and ion-exchange property for metal ions. - Highlights: ► Optimization of radiation dose for grafting reaction of polyethylene with binary monomers. ► Chelating functionalization of grafted film with various amine compounds. ► Characterization of both grafted and chelating functionalized films. ► Proposed mechanism for both grafting and chelating functionalization reaction. ► Application of the synthesized films for the removal of arsenic and some heavy metals from contaminated water.

Characterization of polyester composites from recycled polyethylene terephthalate reinforced with empty fruit bunch fibers

International Nuclear Information System (INIS)

Tan, Chiachun; Ahmad, Ishak; Heng, Muichin

2011-01-01

Highlights: → Unsaturated polyester resin (UPR) was synthesized from recycled PET. → Effect of surface treatment on EFB/UPR was studied. → Treatment on EFB improved the mechanical and thermal properties. → Treatment on EFB also improved fiber-matrix interaction. -- Abstract: Unsaturated polyester resin (UPR) was synthesized from recycled polyethylene terephthalate (PET) which acted as a matrix for the preparation of UPR/empty fruit bunch fibers (EFB) composite. Chemical recycling on fine pieces of PET bottles were conducted through glycolysis process using ethylene glycol. The unsaturated polyester resin (UPR) was then prepared by reacting the glycolysed product with maleic anhydride. FTIR analysis of glycolyzed product and prepared UPR showed that cross-links between unsaturated polyester chain and styrene monomer occurred at the unsaturated sites which resulted in the forming of cross-linking network. The preparation of UPR/EFB composite was carried out by adding EFB into prepared UPR matrix. The effects of surface treatment on EFB with sodium hydroxide solution (NaOH), silane coupling agent and maleic anhydride (MA) were then studied. The experimental results showed that treated EFB have higher values of tensile and impact strength compared with untreated EFB. The best results were obtained for silane treatment followed by MA and NaOH treatments where the tensile strength was increased by about 21%, 18% and 13% respectively. SEM micrographs of the tensile fracture surfaces of UPR/EFB composite also proved that treatment on EFB has increased the interfacial adhesion between the fiber and UPR matrix compared to the untreated UPR/EFB composite.

Seasonal variations of monosaccharide anhydrides in PM1 and PM2.5 aerosol in urban areas

Czech Academy of Sciences Publication Activity Database

Křůmal, Kamil; Mikuška, Pavel; Vojtěšek, Martin; Večeřa, Zbyněk

2010-01-01

Roč. 44, č. 39 (2010), s. 5148-5155 ISSN 1352-2310 R&D Projects: GA MŽP SP/1A3/148/08 Institutional research plan: CEZ:AV0Z40310501 Keywords : monosaccharide anhydrides * biomass burning * levoglucosan Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 3.226, year: 2010

Determination of Glyphosate, Maleic Hydrazide, Fosetyl Aluminum, and Ethephon in Grapes by Liquid Chromatography/Tandem Mass Spectrometry.

Science.gov (United States)

Chamkasem, Narong

2017-08-30

A simple high-throughput liquid chromatography/tandem mass spectrometry (LC-MS-MS) method was developed for the determination of maleic hydrazide, glyphosate, fosetyl aluminum, and ethephon in grapes using a reversed-phase column with weak anion-exchange and cation-exchange mixed mode. A 5 g test portion was shaken with 50 mM HOAc and 10 mM Na 2 EDTA in 1/3 (v/v) MeOH/H 2 O for 10 min. After centrifugation, the extract was passed through an Oasis HLB cartridge to retain suspended particulates and nonpolar interferences. The final solution was injected and directly analyzed in 17 min by LC-MS-MS. Two MS-MS transitions were monitored in the method for each target compound to achieve true positive identification. Four isotopically labeled internal standards corresponding to each analyte were used to correct for matrix suppression effects and/or instrument signal drift. The linearity of the detector response was demonstrated in the range from 10 to 1000 ng/mL for each analyte with a coefficient of determination (R 2 ) of ≥0.995. The average recovery for all analytes at 100, 500, and 2000 ng/g (n = 5) ranged from 87 to 111%, with a relative standard deviation of less than 17%. The estimated LOQs for maleic hydrazide, glyphosate, fosetyl-Al, and ethephon were 38, 19, 29, and 34 ng/g, respectively.

Processing and characterization of Polystyrene/cornstarch/organophilic clay hybrids

International Nuclear Information System (INIS)

Oliveira, Carlos Ivan R. de; Amorim, Ywrrenan C.; Andrade, Cristina T. de

2011-01-01

Polystyrene/cornstarch composite blends with organophilic Cloisite 15A were prepared in an internal mixer in the presence of maleic anhydride (MA). The contents of clay were 1, 3 and 5%, based on the weight of the blend. The results obtained by X-ray diffraction revealed significant intercalation and exfoliation of clay particles within the polymeric moiety, which indicate increased interaction between the components of the nanocomposites. Thermogravimetric analysis results revealed the increase in thermal stability for the compatibilized blends in relation to the noncompatibilized PS/starch blends. The composites showed better thermal stability with increasing clay content. (author)

On the catalytic gas phase oxidation of butadiene to furan

Energy Technology Data Exchange (ETDEWEB)

Kubias, B.; Rodemerck, U. [Institut fuer Angewandte Chemie Berlin-Adlershof e.V., Berlin (Germany); Ritschl, F.; Meisel, M. [Humboldt-Universitaet, Berlin (Germany). Inst. fuer Chemie

1998-12-31

Applying the thermochemical selectivity criterion of Hadnett et al. It is shown that the selectivity of the furan formation is not limited by a too low strength of the C-H bonds in furan when compared with the C-H bond dissociation energy in the educt molecule butadiene. In the oxidation of butadiene on a CsH{sub 2}PMo{sub 12}O{sub 40} catalyst a maximum yield of 22 mol% furan has been obtained. To improve this comparatively low furan yield oxidation activity of the catalyst must be lowered to prevent the consecutive reaction to maleic anhydride. (orig.)

Synthesis and characterization of acrylated Parkia biglobosa medium oil alkyds

Directory of Open Access Journals (Sweden)

E.T. Akintayo

2004-12-01

Full Text Available Acrylated Parkia biglobosa medium oil alkyd prepared by the reaction between an acid containing acrylic copolymer and a monoglyceride followed by the addition of polyol and dibasic acid has been investigated for improved properties. The results revealed that acid functional acrylic copolymers containing maleic anhydride as a functional co-monomer can successfully be used to modify alkyd resins yielding acrylated resins with better drying, flexibility, scratch hardness, impact resistance and chemical resistance properties. However there exist optimum levels for modification of alkyds with such copolymers beyond which certain film properties are adversely affected.

Facile and Efficient Acetylation of Primary Alcohols and Phenols with Acetic Anhydride Catalyzed by Dried Sodium Bicarbonate

Directory of Open Access Journals (Sweden)

Fulgentius Nelson Lugemwa

2013-12-01

Full Text Available A variety of primary alcohols and phenols were reacted with acetic anhydride at room temperature in the presence of sodium bicarbonate to produce corresponding esters in good to excellent yields. The acetylation of 4-nitrobenzyl alcohol was also carried out using other bicarbonates and carbonates. The reaction in the presence of cesium bicarbonate and lithium carbonate gave 4-nitrobenzyl acetate in excellent yield, while in the presence of Na2CO3, K2CO3, Cs2CO3, or KHCO3 the yield was in the range of 80%–95%. Calcium carbonate and cobaltous carbonate did not promote the acetylation of 4-ntirobenzyl alcohol using acetic anhydride. The acetylation of 4-nitrobenzyl alcohol was carried out using ethyl acetate, THF, toluene, diethyl ether, dichloromethane and acetonitrile, and gave good yields ranging from 75%–99%. Toluene was the best solvent for the reaction, while diethyl ether was the poorest.

Incorporating different vegetable oils into an aqueous dispersion of hybrid organic nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Samyn, Pieter, E-mail: Pieter.Samyn@fobawi.uni-freiburg.de [Albert-Luedwigs-University Freiburg, Institute for Forest Utilization (Germany); Schoukens, Gustaaf [Ghent University, Department of Textiles (Belgium); Stanssens, Dirk; Vonck, Leo; Van den Abbeele, Henk [Topchim N.V. (Belgium)

2012-08-15

Different vegetable oils including soy oil, high-oleic sunflower oil, corn oil, castor oil (CO), rapeseed oil, and hydrogenated CO were added to the imidization reaction of poly(styrene-maleic anhydride) or SMA, with ammonium hydroxide in aqueous medium. The oils favorably reduce viscosity during ammonolysis of the anhydride moieties and increase the maximum solid content of the dispersed imidized SMA to at least 50 wt%, compared to a maximum of 35 wt% for pure imidized SMA. The viscosity of imidized SMA with polyunsaturated oils was generally larger than for monosaturated oils, but it was highest for COs due to high contents of hydroxyl groups. Depending on the oil reactivity, homogeneous or core-shell nanoparticles with 20-60 nm diameters formed. The interactions of oil and organic phase were studied by Fourier-transform infrared spectroscopy, indicating qualitative variances between different oils, the fraction imidized SMA and remaining fraction of ammonolyzed SMA without leakage of oil upon diluting the dispersion and precipitation at low pH. A quantitative analysis with calculation of imide contents, amounts of reacted oil and chemical interactions was made by Fourier-transform-Raman spectroscopy suggesting that most interactions take place around the unsaturated oil moieties and ammonolyzed anhydride.

Anhydrides-Cured Bimodal Rubber-Like Epoxy Asphalt Composites: From Thermosetting to Quasi-Thermosetting

Directory of Open Access Journals (Sweden)

Yang Kang

2016-03-01

Full Text Available The present engineering practices show the potential that epoxy asphalt composites (EACs would be a better choice to obtain long life for busy roads. To understand the service performance–related thermorheological properties of prepared bimodal anhydrides-cured rubber-like EACs (REACs, a direct tensile tester, dynamic shear rheometer and mathematical model were used. Tensile tests demonstrate that all the REACs reported here are more flexible than previously reported anhydrides-cured REACs at both 20 and 0 °C. The better flexibility is attributed to the change of bimodal networks, in which cross-linked short chains decreased and cross-linked long chains increased, relatively. Strain sweeps show that all the REACs have linear viscoelastic (LVE properties when their strains are smaller than 1.0% from −35 to 120 °C. Temperature sweeps illustrate that the thermorheological properties of REACs evolve from thermosetting to quasi-thermosetting with asphalt content, and all the REACs retain solid state and show elastic properties in the experimental temperature range. A Cole–Cole plot and Black diagram indicate that all the REACs are thermorheologically simple materials, and the master curves were constructed and well-fitted by the Generalized Logistic Sigmoidal models. This research provides a facile approach to tune the thermorheological properties of the REACs, and the cheaper quasi-thermosetting REAC facilitates their advanced applications.

Characterization of derivates of carbo-anhydride by NMR; Caracterizacao de derivados do anidrido carbico por RMN

Energy Technology Data Exchange (ETDEWEB)

Campos, Marcos Pery Amaral [Instituto Militar de Engenharia (IME), Rio de Janeiro, RJ (Brazil); Bergter, Lothar [Cia. Souza Cruz, Rio de Janeiro, RJ (Brazil); Seidl, Peter Rudolf [Centro de Tecnologia Mineral, Rio de Janeiro, RJ (Brazil)

1994-12-31

The term molecular recognition may be applied to several phenomena of different complexities. The compounds which work as blockers or acceptors in this process are generally complexes with functional groups positioned in specific positions. This work presents the NMR characterization of carbo-anhydride derivates which are important in the preparation of synthetic acceptors 2 figs.

Kinetics of Hydrolysis of Acetic Anhydride by In-Situ FTIR Spectroscopy: An Experiment for the Undergraduate Laboratory

Science.gov (United States)

Haji, Shaker; Erkey, Can

2005-01-01

A reaction kinetics experiment for the chemical engineering undergraduate laboratory course was developed in which in-situ Fourier Transfer Infrared spectroscopy was used to measure reactant and product concentrations. The kinetics of the hydrolysis of acetic anhydride was determined by experiments carried out in a batch reactor. The results…

Purifying, concentrating and anhydriding bio-ethanol: Alternative process schemes and innovative separation methods

International Nuclear Information System (INIS)

Guerreri, G.; Lovati, A.

1992-01-01

Starting with the conventional process scheme for bio-ethanol production, this paper illustrates how the anhydriding section, which incorporates an azeotropic distillation process, can be conveniently substituted with a plate and frame pervaporation process which makes use of optimum heat exchange with the stripping section. This technical feasibility study, which proves the superior energy efficiency of the pervaporation scheme as compared with the conventional scheme, is followed by a cost benefit analysis which evidences the economic benefits also to be had with pervaporation

Development of Transparent Materials Which Reduce Effects of Precipitation Static in Aircraft

Science.gov (United States)

1952-03-01

table shows the acid numbers of some available compounds: Polymer Acid Number Polyacrylic acid 780 Polymethacrylic acid 653 1:1 Styrene-maleic acid ...orthophosphoric acid in polymethyl methacrylate and analogous systems merit further detailed investigation. PUBLICATION REVIEW Manuscript Copy of this report...Resins 74 4.4 Polyacrylic Acid Films 76 4.5 Films of the Ammonium Salt of Styrene- Maleic Acid Copolymer 76 4.6 Imidization 80 4.7 Vinyl Addition 81 4.8

Investigation of the ageing effects on phenol-urea-formaldehyde binder and alkanol amine-acid anhydride binder coated mineral fibres

DEFF Research Database (Denmark)

Zafar, Ashar; Schjødt-Thomsen, Jan; Sodhi, R.

2013-01-01

-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) were employed to identify the chemical changes occurring in the PUF binder coated mineral fibres and alkanol amine-acid anhydride binder coated mineral fibres during that ageing. The samples were aged in a climate......Phenol-Urea-Formaldehyde (PUF) binder coated mineral fibres' mechanical properties have been observed to degrade during ageing at elevated temperatures and humidity, while alkanol amine-acid anhydride binder based mineral fibres exhibited better ageing properties for same duration of ageing. X...... chamber for 7 days at 70 °C and 95% relative humidity. In the case of the PUF binder coated fibres, quantitative XPS measurements showed some significant changes in the atomic composition of the PUF binder coated mineral fibres after ageing, including decreased urea and carbonyl groups concentrations...

Thermal analysis and its application in evaluation of fluorinated polyimide membranes for gas separation

KAUST Repository

Qiu, Wulin

2011-08-01

Seven polyimides based on (4,4′-hexafluoroisopropylidene) diphthalic anhydride, 6FDA, with different chemical structures were synthesized in a single pot two-step procedure by first producing a high molecular weight polyamic acid (PAA), followed by reaction with acetic anhydride to produce polyimide (PI). The resulting polymers were characterized using thermal analysis techniques including TGA, derivative weight analysis, TGA-MS, and DSC. The decarboxylation-induced thermal cross-linking, ester cross-linking through a diol, and ion-exchange reactions of selected polyimide membranes were investigated. Cross-linking of polymer membranes was confirmed by solubility tests and CO 2 permeability measurements. The thermal analysis provides simple and timesaving opportunities to characterize the polymer properties, the ability to optimize polymer cross-linking conditions, and to monitor polymer functionalization to develop high performance polymeric membranes for gas separations. © 2011 Elsevier Ltd. All rights reserved.

Thermal and electrical properties of polymers produced from methyl oleate and bio diesel of sunflower and linseed oils

International Nuclear Information System (INIS)

Nicolau, Aline; Reiznautt, Quelen B.; Martini, Denise D.; Samios, Dimitrios

2011-01-01

Polyesters were prepared from epoxidized biodiesel with different unsaturation degrees. The polymerisation was performed using epoxidized methyl esters of oleic acid (EPOAME), sunflower oil (EPSOME) and linseed oil (EPLOME) with cis-1,2-cyclohexanedicarboxylic anhydride and triethylamine. Differential Scanning Calorimetry (DSC) demonstrated that reaction enthalpy was proportional to the unsaturation degree of each methyl ester. With an increase in unsaturation degree, the activation energy linearly decreased. The intermediate structures and the polyesters were characterised using Nuclear Magnetic Resonance (NMR) techniques. The molecular weight of the polymers synthesised with EPOAME, EPSOME and EPLOME were, respectively, 2.5x103, 5.3x103 and 14x103 g/mol. The glass transition of the product obtained from EPOAME was -59 degree C. The polymers based on EPSOME and EPLOME exhibited higher Tg values, which were -11 and -6 degree C, respectively. Electric impedance measurements of the polyesters showed that an increase in unsaturation degree resulted in an increase in resistivity and a decrease in capacitance. (author)

High performances unsaturated polyester based nanocomposites: Effect of vinyl modified nanosilica on mechanical properties

Directory of Open Access Journals (Sweden)

J. D. Rusmirovic

2016-02-01

Full Text Available Influences of the vinyl modified nanosilica Aerosil® 380, i.e./i>, vinyl and methacryloyl silane coupling agent and linseed oil fatty acids (BD reactive residues, on the mechanical properties of the unsaturated polyester resins (UPes based nanocomposites, was studied. The polycondensation of maleic anhydride and products of poly(ethylene terephthalate (PET depolymerization with propylene glycol, with and without separation of ethylene glycol, yields UPe1 and UPe2 resin, respectively. The hydroxyl terminated PET depolymerization products (glycolyzates and UPes were characterized by acid and hydroxyl values, Fourier Transform Infrared (FTIR and nuclear magneti resonance (NMR spectroscopies. Transmission electron microscopy (TEM confirmed that silica nanoparticles formed domains of aggregates in the polymer matrix. An increase from 195 to 247% of stress at break (σb, and from 109 to 131% of impact strength (σi of UPes based nanocomposites was obtained for 1 wt% addition of vinyl modified silica. Flexural strength (σf increase from 106 to 156% for both UPes based nanocomposites with 1 wt% addition of BD modified silica. Cross-linking density (ν, storage modulus (G', tanδ and Tg of the nanocomposite were determined from the dynamic mechanical testing and discussed in relation to the structure of silica modification.

Thermoplastic Elastomers From Chemically or Irradiation Activated Polyolefin Wastes and Ground Tyre Rubber

International Nuclear Information System (INIS)

Tolstov, A.M.; Grigoryeva, A.L.; Bardash, O.P.

2005-01-01

Thermoplastic elastomers (TPE) are known as materials with unique combination of elastomeric properties and thermo plasticity. Among the TPE of different type the polymer blends of thermoplastics and rubbers are the most commonly used. Recently a very effective technology of dynamic vulcanization of rubber component inside thermoplastic matrix has been developed. As a result of rubber vulcanization and dispersion inside thermoplastic the new type of TPE so-called thermoplastic dynamic vulcanizations (TPV) are obtained. In our work we have applied the technology of dynamic vulcanization for recycled components (PP, HDPE, GTR). It has appeared that such components are not mixed well and the resulting TPV have poor mechanical properties. To solve a problem of poor compatibility of the components used we carried out a pre-modification (functionalization) of the component surfaces by gamma-irradiation or by chemically or gamma-irradiation induced grafting of reactive monomers. Both the polyolefin (HDPE) and GTR were functionalized before mixing. The monomers were selected by such a way that being grafted to be able to react to each other in interface during the components blending. For example, we used maleic anhydride and acrylamide. The effect of better compatibility has appeared in higher tensile characteristics of TPV synthesized

Impact of Surface Modification and Nanoparticle on Sisal Fiber Reinforced Polypropylene Nano composites

International Nuclear Information System (INIS)

Ibrahim, I. D.; Jamiru, T.; Sadiku, E. R.; Agwuncha, S. Ch.; Kupolati, W. K.

2016-01-01

The use of plant fibers, polymer, and nanoparticles for composite has gained global attention, especially in the packaging, automobile, aviation, building, and construction industries. Nano composites materials are currently in use as a replacement for traditional materials due to their superior properties, such as high strength-to-weight ratio, cost effectiveness, and environmental friendliness. Sisal fiber (SF) was treated with 5% NaOH for 2 hours at 70"°C. A mixed blend of sisal fiber and recycled polypropylene (rPP) was produced at four different fiber loadings: 10, 20, 30, and 40 wt.%, while nano clay was added at 1, 3, and 5 wt.%. Maleic anhydride grafted polypropylene (MAPP) was used as the compatibilizer for all composites prepared except the untreated sisal fibers. The characterization results showed that the fiber treatment, addition of MAPP, and nano clay improved the mechanical properties and thermal stability and reduced water absorption of the SF/rPP nano composites. The tensile strength, tensile modulus, and impact strength increased by 32.80, 37.62, and 5.48%, respectively, when compared to the untreated SF/rPP composites. Water absorption was reduced due to the treatment of fiber and the incorporation of MAPP and nano clay.

Feedback-mediated cancer therapy: a FRET-based nanoreporter approach

Science.gov (United States)

Sarkar, Suproteem K.; Khater, Yashika; Kulkarni, Ashish; Sengupta, Shiladitya

2014-08-01

A theranostic nanoparticle system was developed by integrating a chemotherapeutic agent with an "activatable" fluorescent tracer. The system signals tumor death by monitoring the activity of caspase-3, a product of apoptosis, and can therefore screen the treatment sensitivity of a particular tumor. The polymer nanoparticles (Poly [isobutylene-alt-maleic anhydride]) were formed through reprecipitation and contained paclitaxel, a chemotherapy drug, and fluorescein isothiocyanate, a fluorescent dye. The dye's fluorescence was quenched through Förster resonance energy transfer (FRET) by a quencher that was connected to the dye by a peptide chain. With sizes ranging from 200-250 nm, the nanoparticles were stable for two weeks. The nanoparticles were tested in vitro with responsive Lewis Lung Carcinoma (LLC) cells and taxane-resistant cells. Upon cell death by paclitaxel exposure, caspase-3 cleaved the peptide chain connecting the dye and the quencher, causing the system to fluoresce. When LLC cells were treated with the system, the nanoreporters fluoresced, but when resistant cells were tested, and when the drug was removed from the system, the nanoreporters did not fluoresce. Since the system screens if a drug can successfully kill a particular tumor, it offers a novel and promising approach to personalized medicine.

The Effect of wheat straw particle size on the mechanical and water absorption properties of wheat straw/low density polyethylene biocomposites for packaging applications

Directory of Open Access Journals (Sweden)

Behjat Tajeddin

2017-08-01

Full Text Available Natural composites with biodegradability properties can be used as a renewable alternative to replacing conventional plastics. Thus, to reduce the plastics applications in the packaging industry, biocomposites content of wheat straw (with 40, 100, 140 mesh as a natural biodegradable composite and low density polyethylene (LDPE as a common synthetic polymer in the packaging industry were prepared and characterized by the mechanical and water absorption properties. Polyethylene-graft-maleic anhydride was used as a compatibilizer material. Morphology of wheat straw flour was studied by optical microscope to obtain the aspect ratio (L/D. The tensile and flexural tests were applied for determining mechanical properties and scanning electron microscope (SEM was used for particles distribution and sample structures. The water absorption of the samples was calculated by weight difference. The results indicated that the particle size of wheat straw four and the L/D amount are Significantly affected on the tensile strength and water absorption of the samples. However, the effect of wheat sraw particle size on the flexural strength was not significant. Overall conclusions show that by increasing the particle size of the filler (wheat straw, can prepare the biocomposite with better tensile strength and less water absorption compared with smaller particle size.

Poly(Lactic Acid) Filled with Cassava Starch-g-Soybean Oil Maleate

Science.gov (United States)

Kiangkitiwan, Nopparut; Srikulkit, Kawee

2013-01-01

Poly(lactic acid), PLA, is a biodegradable polymer, but its applications are limited by its high cost and relatively poorer properties when compared to petroleum-based plastics. The addition of starch powder into PLA is one of the most promising efforts because starch is an abundant and cheap biopolymer. However, the challenge is the major problem associated with poor interfacial adhesion between the hydrophilic starch granules and the hydrophobic PLA, leading to poorer mechanical properties. In this paper, soybean oil maleate (SOMA) was synthesized by grafting soybean oil with various weight percents of maleic anhydride (MA) using dicumyl peroxide (DCP) as an initiator. Then, SOMA was employed for the surface modifying of cassava starch powder, resulting in SOMA-g-STARCH. The obtained SOMA-g-STARCH was mixed with PLA in various weight ratios using twin-screw extruder, resulting in PLA/SOMA-g-STARCH. Finally, the obtained PLA/SOMA-g-STARCH composites were prepared by a compression molding machines. The compatibility, thermal properties, morphology properties, and mechanical properties were characterized and evaluated. The results showed that the compatibility, surface appearance, and mechanical properties at 90 : 10 and 80 : 20 ratios of PLA/SOMA-g-STARCH were the best. PMID:24307883

Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate

Directory of Open Access Journals (Sweden)

Hess Sonia C.

2000-01-01

Full Text Available Ozonolysis of maleopimaric anhydride methyl ester in the presence of tetracyanoethylene led to an epoxide and an ozonide. Ozonolysis of the trimethyl fumaropimarate, followed by treatment with Me2S, led to an epoxide, a diene, a keto-acid and an allylic oxidation product. Some of the compounds obtained were active against Staphylococcus aureus, Bacillus subtilis and Micrococcus luteus.

RAFT copolymerization of itaconic anhydride and 2-methoxyethyl acrylate: a multifunctional scaffold for preparation of “clickable” gold nanoparticles

DEFF Research Database (Denmark)

Javakhishvili, Irakli; Kasama, Takeshi; Jankova, Katja Atanasova

2013-01-01

RAFT copolymerization of 2-methoxyethyl acrylate and itaconic anhydride – a monomer derived from renewable resources – is carried out in a controlled fashion. The copolymer allows preparation of gold nanoparticles with abundant surficial carboxyl and alkyne functional groups that are dendronized...

Membrane polypeptide in rabbit erythrocytes associated with the inhibition of L-lactate transport by a synthetic anhydride of lactic acid

International Nuclear Information System (INIS)

Donovan, J.A.; Jennings, M.L.

1985-01-01

The synthetic lactyl anhydride isobutylcarbonyl lactyl anhydride (iBCLA), a selective and potent inhibitor of L-(+)-lactate transport in rabbit erythrocytes, reduces the chemical labeling of a 40-50-kdalton polypeptide by tritiated 4,4'-diisothiocyanato-2,2'-dihydrostilbenedisulfonate ([ 3 H]H 2 DIDS). iBCLA does so in a dose-dependent manner at concentrations that strongly inhibit lactate-lactate exchange but not chloride-phosphate exchange. These labeling experiments and inhibition reversal studies using iBCLA, p-(chloro-mercuri)benzenesulfonic acid (pCMBS), and dithiothreitol (DDT) suggest that iBCLA does not act at sulfhydryl groups but at or near an amino group that is near a disulfide linkage in the polypeptide which catalyzes lactate transport. These experiments support the association between specific monocarboxylate transport and a 40-50-kdalton membrane-bound polypeptide of the rabbit erythrocyte

Laser-induced photochemical reaction of aqueous maleic acid solutions containing H2O2

International Nuclear Information System (INIS)

Shimizu, Yuichi; Kawanishi, Shunichi; Suzuki, Nobutake

1995-01-01

Hydroxy acid such as glycolic, tartaric and malic acids was directly produced by XeF-laser irradiation of the N 2 -saturated maleic acid aqueous solution containing H 2 O 2 . The selectivities of these products at the maximum of tartaric acid were 71, 4, and 2% at H 2 O 2 feeding rate of 3.2 ml h -1 , respectively. On the other hand, the irradiation of maleates such as dipotassium, calcium, and disodium greatly enhanced the selectivities of tartaric acid formation to 19%, and of malic acid formation to 13%, respectively, for dipotassium maleate. It may be considered from these results that the stability of the hydroxylated intermediate radical plays an important role for the efficient formations of tartaric and malic acids. (author)

Nanocomposites of polypropylene and organophilic montmorillonite clay: X-ray diffraction, infrared spectroscopy with Fourier transform and water permeation;Nanocomposito de prolipropileno e argila montmorilonita organifilica: difracao de raios-X, espectroscopia na regiao do infravermelho e permeacao ao vapor de agua

Energy Technology Data Exchange (ETDEWEB)

Morelli, Fernanda C; Ruvolo Filho, Adhemar, E-mail: fer_morelli@yahoo.com.b, E-mail: adhemar@power.ufscar.b [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil)

2009-07-01

In this work were prepared nanocomposites of polypropylene and organophilic montmorillonite Cloisite 20A with concentrations of 1.5%, 2.5%, 5.0% and 7.5% clay and graft polypropylene with maleic anhydride as compatibilizer. The mixture was made in the melt state using a twin screw extruder. The materials were characterized by x-ray diffraction, infrared spectroscopy with Fourier transform and analysis of water vapor permeation. The results of x-ray diffraction and infrared spectroscopy indicates the formation of nanocomposites with structures probably exfoliate and / or intercalated for concentrations of 1.5% and 2.5% clay, and provided a marked decrease in the water permeability, corroborating with other analysis. (author)

Nuclear magnetic resonance structure investigations on crosslinked polyesters

International Nuclear Information System (INIS)

Grobelny, J.

1999-01-01

Styrene-crosslinked mixed polyesters derived from maleic anhydride, 2,2-di(4-hydroxypropoxyphenyl)propane, oligo(propylene oxide) and 1,2-propylene glycol were investigated by high-resolution solid-state 13 C NMR spectroscopy. The structural modifications accompanying crosslinking were characterized in terms of spin-lattice relaxation times as a function of unsaturated polyester composition. Copolymerization and crosslinking effects were individually evaluated and the latter effect was related to variations in crosslinking density associated with the chemical structure of the unsaturated prepolymer. As the crosslinking effect is suppressed, the mechanical properties undergo expected changes, e.g., impact strength is increased and modulus of elasticity in tension is decreased. (author)

Nanocomposites of polypropylene and organophilic montmorillonite clay: X-ray diffraction, infrared spectroscopy with Fourier transform and water permeation

International Nuclear Information System (INIS)

Morelli, Fernanda C.; Ruvolo Filho, Adhemar

2009-01-01

In this work were prepared nanocomposites of polypropylene and organophilic montmorillonite Cloisite 20A with concentrations of 1.5%, 2.5%, 5.0% and 7.5% clay and graft polypropylene with maleic anhydride as compatibilizer. The mixture was made in the melt state using a twin screw extruder. The materials were characterized by x-ray diffraction, infrared spectroscopy with Fourier transform and analysis of water vapor permeation. The results of x-ray diffraction and infrared spectroscopy indicates the formation of nanocomposites with structures probably exfoliate and / or intercalated for concentrations of 1.5% and 2.5% clay, and provided a marked decrease in the water permeability, corroborating with other analysis. (author)

Thermal analysis of polypropylene modified by gamma irradiation composites under outdoor conditions

International Nuclear Information System (INIS)

Komatsu, Luiz G.H.; Oliani, Washington L.; Lugao, Ademar B.; Parra, Duclerc F.

2015-01-01

This work reports the influence of the clay in the degradation process of the HMSPP.The polypropylene (PP) was irradiated under acetylene atmosphere in gamma irradiation source ( 60 Co) to obtain the HMSPP (high melt strength polypropylene). Composites of HMSPP were processed in twin-screw extruder with clay Cloisite 20A and Maleic Anhydride (PP-g-MA) as coupling agent. The obtained composites were exposed under outdoor conditions for 6 months. The ageing effects were characterized by Differential Scanning Calorimetry (DSC), Thermogravimetry Analysis (TGA). Chemical oxidation was evaluated by Carbonyl Index (IC) through infrared Spectroscopy (FT-IR). The results showed correlation between carbonyl index and ageing time. (author)

Thermal analysis of polypropylene modified by gamma irradiation composites under outdoor conditions

Energy Technology Data Exchange (ETDEWEB)

Komatsu, Luiz G.H.; Oliani, Washington L.; Lugao, Ademar B.; Parra, Duclerc F., E-mail: dfparra@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2015-07-01

This work reports the influence of the clay in the degradation process of the HMSPP.The polypropylene (PP) was irradiated under acetylene atmosphere in gamma irradiation source ({sup 60}Co) to obtain the HMSPP (high melt strength polypropylene). Composites of HMSPP were processed in twin-screw extruder with clay Cloisite 20A and Maleic Anhydride (PP-g-MA) as coupling agent. The obtained composites were exposed under outdoor conditions for 6 months. The ageing effects were characterized by Differential Scanning Calorimetry (DSC), Thermogravimetry Analysis (TGA). Chemical oxidation was evaluated by Carbonyl Index (IC) through infrared Spectroscopy (FT-IR). The results showed correlation between carbonyl index and ageing time. (author)

Synthesis and antimicrobial activities of new 4-thiazolidones derived from formipyridine thiosemicarbazones; Sintese e avaliacao da atividade antimicrobiana de novas 4-tiazolidinonas obtidas a partir de formilpiridina tiossemicarbazonas

Energy Technology Data Exchange (ETDEWEB)

Vercoza, George Leonardo; Feitoza, Danniel Delmondes; Alves, Antonio Jose; Aquino, Thiago Mendonca de; Lima, Jose Gildo de [Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil). Dept. de Ciencias Farmaceuticas], e-mail: jgildolima@gmail.com; Araujo, Janete Magali; Cunha, Ivana Glaucia B.; Goes, Alexandre Jose da Silva [Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil). Dept. de Antibioticos

2009-07-01

Twelve novel 4-thiazolidinone derivatives (2a-l) have been synthesized by reacting formylpyridine thiosemicarbazones (1a-l) and anhydride maleic in toluene. Their chemical structures were confirmed by IR, {sup 1}H and {sup 13}C NMR. The new compounds were submitted to in vitro evaluation against pathogenic Gram-positive, Gram-negative bacteria and yeasts. The findings obtained showed that the compounds 2a, 2d, 2e and 2g were effective against some of the bacterial strains used, whereas the compounds 2d, 2e and 2i exhibited a moderate antifungal activity against the yeast strains evaluated. An initial structure activity relationship (SAR) was established. (author)

Synthesis and antimicrobial activities of new 4-thiazolidones derived from formipyridine thiosemicarbazones

International Nuclear Information System (INIS)

Vercoza, George Leonardo; Feitoza, Danniel Delmondes; Alves, Antonio Jose; Aquino, Thiago Mendonca de; Lima, Jose Gildo de; Araujo, Janete Magali; Cunha, Ivana Glaucia B.; Goes, Alexandre Jose da Silva

2009-01-01

Twelve novel 4-thiazolidinone derivatives (2a-l) have been synthesized by reacting formylpyridine thiosemicarbazones (1a-l) and anhydride maleic in toluene. Their chemical structures were confirmed by IR, 1 H and 13 C NMR. The new compounds were submitted to in vitro evaluation against pathogenic Gram-positive, Gram-negative bacteria and yeasts. The findings obtained showed that the compounds 2a, 2d, 2e and 2g were effective against some of the bacterial strains used, whereas the compounds 2d, 2e and 2i exhibited a moderate antifungal activity against the yeast strains evaluated. An initial structure activity relationship (SAR) was established. (author)

Atypical cleavage of protonated N-fatty acyl amino acids derived from aspartic acid evidenced by sequential MS3 experiments.

Science.gov (United States)

Boukerche, Toufik Taalibi; Alves, Sandra; Le Faouder, Pauline; Warnet, Anna; Bertrand-Michel, Justine; Bouchekara, Mohamed; Belbachir, Mohammed; Tabet, Jean-Claude

2016-12-01

Lipidomics calls for information on detected lipids and conjugates whose structural elucidation by mass spectrometry requires to rationalization of their gas phase dissociations toward collision-induced dissociation (CID) processes. This study focused on activated dissociations of two lipoamino acid (LAA) systems composed of N-palmitoyl acyl coupled with aspartic and glutamic acid mono ethyl esters (as LAA (*D) and LAA (*E) ). Although in MS/MS, their CID spectra show similar trends, e.g., release of water and ethanol, the [(LAA (*D/*E) +H)-C 2 H 5 OH] + product ions dissociate via distinct pathways in sequential MS 3 experiments. The formation of all the product ions is rationalized by charge-promoted cleavages often involving stepwise processes with ion isomerization into ion-dipole prior to dissociation. The latter explains the maleic anhydride or ketene neutral losses from N-palmitoyl acyl aspartate and glutamate anhydride fragment ions, respectively. Consequently, protonated palmitoyl acid amide is generated from LAA (*D), whereas LAA (*E) leads to the [*E+H-H 2 O] + anhydride. The former releases ammonia to provide acylium, which gives the C n H (2n-1) and C n H (2n-3) carbenium series. This should offer structural information, e.g., to locate either unsaturation(s) or alkyl group branching present on the various fatty acyl moieties of lipo-aspartic acid in further studies based on MS n experiments.

Preparation of Polypropylene/Montmorillonite Nanocomposites Using Ionizing Radiation

International Nuclear Information System (INIS)

Güven, Olgun; Zengin, Fatma

2011-01-01

Polymer/clay nanocomposites are new generation materials that bring significant changes in mechanical, thermal and permeation properties of base polymers by low clay loading. In this study, polypropylene/montmorillonite nanocomposites were prepared by melt intercalation method by using batch type mixer. Two polypropylene samples with different melt flow indexes are used as the matrix, maleic anhydride grafted polypropylene (PP-g-MAH), and polypropylene granules oxidized by radiation/ozone are used as compatibilizer and unmodified clay (Na + montmorillonite, MMT) as the filler. Aim of this study is to examine the effect of different compatibilizers in the mechanical properties of polypropylene composite. Firstly, PP/clay samples were prepared and the effect of clay was examined, then 5, 10, 20kGy oxidized/degraded polypropylenes were used as compatibilizer and, 10 kGy was determined to be the most suitable irradiation dose for the best compatibilizing effect. Polypropylene granules were ozonated until they contained carbonyl groups equivalent to 10kGy oxidized PP, which was checked by FTIR-ATR spectroscopy. UV-visible reflectance measurements were also made on film samples and no significant changes were observed in visible region. Nano structures of some nanocomposites were characterized by PALS (Positron Annihilation Lifetime Spectroscopy) where it was observed that the addition of clay decreased the number of free volume holes and free volume hole radia. The dispersion state of MMT within polymer matrix was analyzed by XRD (X-ray diffraction). Tensile tests were made and the effect of the addition of clay and compatibilizers investigated. At low melt flow index PP, 1% MMT of PP/10kGyPP/MMT nanocomposite showed an increase in E-modulus 26% and in tensile strength 8% as compared to those of pristine PP. In conclusion radiation degraded (chain scissioned and oxidized) PP has been found to show very good compatibilizing effect for the natural montmorillonite

Preparation, characterization, and antibacterial activity of NiFe{sub 2}O{sub 4}/PAMA/Ag–TiO{sub 2} nanocomposite

Energy Technology Data Exchange (ETDEWEB)

Allafchian, Alireza, E-mail: Allafchian@cc.iut.ac.ir [Nanotechnology and Advanced Materials Institute, Isfahan University of Technology, Isfahan 84156–83111 (Iran, Islamic Republic of); Jalali, Seyed Amir Hossein [Institute of Biotechnology and Bioengineering, Isfahan University of Technology, Isfahan 84156–83111 (Iran, Islamic Republic of); Department of Natural Resources, Isfahan University of Technology, Isfahan 84156–83111 (Iran, Islamic Republic of); Bahramian, Hamid; Ahmadvand, Hossein [Department of physics, Isfahan University of Technology, Isfahan 84156–83111 (Iran, Islamic Republic of)

2016-04-15

We have described a facile fabrication of silver deposited on the TiO{sub 2}, Poly Acrylonitrile Co Maleic Anhydride (PAMA) polymer and nickel ferrite composite (NiFe{sub 2}O{sub 4}/PAMA/Ag–TiO{sub 2}) through a three-step procedure. A pre-synthesized NiFe{sub 2}O{sub 4} was first coated with PAMA polymer and then Ag–TiO{sub 2} was deposited on the surface of PAMA polymer shell. After the characterization of this three-component composite by various techniques, such as FTIR, XRD, FESEM, BET, TEM and VSM, it was impregnated in standard antibiotic discs. The antibacterial activity of NiFe{sub 2}O{sub 4}/PAMA/Ag–TiO{sub 2} nanocomposite was investigated against some gram positive and gram negative bacteria by employing disc diffusion assay and then compared with that of naked NiFe{sub 2}O{sub 4}, NiFe{sub 2}O{sub 4}/Ag, AgNPs and NiFe{sub 2}O{sub 4}/PAMA. The results demonstrated that the AgNPs, when embedded in TiO{sub 2} and combined with NiFe{sub 2}O{sub 4}/PAMA, became an excellent antibacterial agent. The NiFe{sub 2}O{sub 4}/PAMA/Ag–TiO{sub 2} nanocomposite could be readily separated from water solution after the disinfection process by applying an external magnetic field. - Highlights: • A novel NiFe{sub 2}O{sub 4}/PAMA/Ag–TiO{sub 2} magnetic nanocomposite has been prepared. • This nanocomposite displays potent antimicrobial activity. • The antibacterial effect was evaluated by the disk diffusion method. • Recyclable antibacterial activity of NiFe{sub 2}O{sub 4}/PAMA/Ag–TiO{sub 2} was studied.

Preparation of Polypropylene/Montmorillonite Nanocomposites Using Ionizing Radiation

Energy Technology Data Exchange (ETDEWEB)

Güven, Olgun; Zengin, Fatma

2011-07-01

Polymer/clay nanocomposites are new generation materials that bring significant changes in mechanical, thermal and permeation properties of base polymers by low clay loading. In this study, polypropylene/montmorillonite nanocomposites were prepared by melt intercalation method by using batch type mixer. Two polypropylene samples with different melt flow indexes are used as the matrix, maleic anhydride grafted polypropylene (PP-g-MAH), and polypropylene granules oxidized by radiation/ozone are used as compatibilizer and unmodified clay (Na{sup +} montmorillonite, MMT) as the filler. Aim of this study is to examine the effect of different compatibilizers in the mechanical properties of polypropylene composite. Firstly, PP/clay samples were prepared and the effect of clay was examined, then 5, 10, 20kGy oxidized/degraded polypropylenes were used as compatibilizer and, 10 kGy was determined to be the most suitable irradiation dose for the best compatibilizing effect. Polypropylene granules were ozonated until they contained carbonyl groups equivalent to 10kGy oxidized PP, which was checked by FTIR-ATR spectroscopy. UV-visible reflectance measurements were also made on film samples and no significant changes were observed in visible region. Nano structures of some nanocomposites were characterized by PALS (Positron Annihilation Lifetime Spectroscopy) where it was observed that the addition of clay decreased the number of free volume holes and free volume hole radia. The dispersion state of MMT within polymer matrix was analyzed by XRD (X-ray diffraction). Tensile tests were made and the effect of the addition of clay and compatibilizers investigated. At low melt flow index PP, 1% MMT of PP/10kGyPP/MMT nanocomposite showed an increase in E-modulus 26% and in tensile strength 8% as compared to those of pristine PP. In conclusion radiation degraded (chain scissioned and oxidized) PP has been found to show very good compatibilizing effect for the natural montmorillonite

Kerogen chemistry 5. Anhydride formation in, solvent swelling of, and loss of organics on demineralization of Kimmeridge shales

International Nuclear Information System (INIS)

Larsen, John W.; Flores, Carlos Islas

2008-01-01

The results of three short and related, but experimentally independent, studies of 4 Kimmeridge shales and their kerogens are reported. Differential scanning calorimeter (DSC) studies of the kerogens reveal that three of the four show evidence of anhydride formation when heated at 20 C/min between 50 C and 180 C. There is no regular rank dependence of anhydride formation. After solvent swelling in tetrahydrofuran (THF), extracted organics were isolated from the THF and the recovered kerogens were swollen a second time in fresh THF. The second solvent swelling ratios were slightly larger than the first because the presence of the extracts in the original THF lowers solvent activity thus reducing swelling. The shales were demineralized in the usual way except that methylene chloride was added to dissolve any organics that were liberated from the rock as a consequence of mineral dissolution. Small amounts of organics were found in the methylene chloride supporting Price and Clayton's conclusion that organics are expelled from the kerogen and are present in lacunae in the minerals. (author)

The effectiveness of styrene-maleic acid (SMA) copolymers for solubilisation of integral membrane proteins from SMA-accessible and SMA-resistant membranes.

Science.gov (United States)

Swainsbury, David J K; Scheidelaar, Stefan; Foster, Nicholas; van Grondelle, Rienk; Killian, J Antoinette; Jones, Michael R

2017-10-01

Solubilisation of biological lipid bilayer membranes for analysis of their protein complement has traditionally been carried out using detergents, but there is increasing interest in the use of amphiphilic copolymers such as styrene maleic acid (SMA) for the solubilisation, purification and characterisation of integral membrane proteins in the form of protein/lipid nanodiscs. Here we survey the effectiveness of various commercially-available formulations of the SMA copolymer in solubilising Rhodobacter sphaeroides reaction centres (RCs) from photosynthetic membranes. We find that formulations of SMA with a 2:1 or 3:1 ratio of styrene to maleic acid are almost as effective as detergent in solubilising RCs, with the best solubilisation by short chain variants (membranes was uniformly low, but could be increased through a variety of treatments to increase the lipid:protein ratio. However, proteins isolated from such membranes comprised clusters of complexes in small membrane patches rather than individual proteins. We conclude that short-chain 2:1 and 3:1 formulations of SMA are the most effective in solubilising integral membrane proteins, but that solubilisation efficiencies are strongly influenced by the size of the target protein and the density of packing of proteins in the membrane. Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.

Efficient synthesis of zinc-containing mesoporous silicas by microwave irradiation method and their high activities in acetylation of 1,2-dimethoxybenzene with acetic anhydride

Directory of Open Access Journals (Sweden)

K. Bachari

2016-09-01

Full Text Available A series of acid zinc-containing mesoporous materials have been synthesized by microwave irradiation method with different Si/Zn ratios (Si/Zn = 100, 65, 15 and characterized by several spectroscopic techniques such as: N2 physical adsorption, ICP, XRD, TEM, FT-IR and a temperature-programmed-desorption (TPD of pyridine. The liquid phase of acetylation of 1,2-dimethoxybenzene with acetic anhydride has been investigated over this series of catalysts. In fact, the catalyst Zn-JLU-15 (15 showed bigger performance in the acid-catalyzed acetylation of 1,2-dimethoxybenzene employing acetic anhydride as an acylating agent. Furthermore, the kinetics of the acetylation of 1,2-dimethoxybenzene over these catalysts have also been investigated.

Study on radiation-induced polymerization of vinyl monomers adsorbed on inorganic substances. II. Radiation-induced polymerization of methyl methacrylate adsorbed on several inorganic substances

International Nuclear Information System (INIS)

Fukano, K.; Kageyama, E.

1975-01-01

The radiation-induced polymerization of methyl methacrylate (MMA) adsorbed on such inorganic substances as silica gel, white carbon, silicic acid anhydride, zeolite, and activated alumina was carried out to compare with the case of styrene. The rate of radiation-induced polymerization adsorbed on inorganic substances was high compared with that of radiation-induced bulk state polymerization, as was the case with styrene. Inorganic substrates which contain aluminum as a component element are more likely to be grafted than those which consist of SiO 2 alone, as with styrene. The molecular weight distribution of unextractable polymer and extractable polymer differs, depending on the type of inorganic substance. Experiments by a preirradiation method were carried out in case of silica gel, white carbon, and silicic acid anhydride. GPC spectra of the polymer obtained were different from those of polymer formed by the simultaneous irradiation method. It appears that all the unextractable polymer is grafted to the inorganic surface with chemical bond

Nanocompósitos de polietileno/argila bentonita nacional: influência da argila e do agente compatibilizante PE-g-MA nas propriedades mecânicas e de inflamabilidade Polyethylene/national bentonite clay nanocomposites: influence of clay and PE-g-MA coupling agent on the mechanical properties and flammability

Directory of Open Access Journals (Sweden)

Gustavo F. Brito

2008-06-01

higher tensile modulus and torque value. The flammability test showed that the addition of clay in the polymer matrix and PE-g-MA reduced the burning rate, indicating an improved flammability resistance of the nanocomposites. In general, the system containing PE-g-MA coupling agent led to partially exfoliated nanocomposites with higher thermal stability than the high density polyethylene matrix. The polyethylene-graft-maleic anhydride promoted the exfoliation of clay and adhesion between matrix and filler, thus resulting in enhanced mechanical properties.

Greener Friedel-Crafts Acylation using Microwave-enhanced reactivity of Bismuth Triflate in the Friedel-Crafts Benzoylation of Aromatic Compounds with Benzoic Anhydride

DEFF Research Database (Denmark)

Tran, Phuong Hoang; Nguyen, Hai Truong; Hansen, Poul Erik

2017-01-01

An efficient and facile bismuth trifluoromethanesulfonate-catalyzed benzoylation of aromatic compounds using benzoic anhydride under solvent-free microwave irradiation has been developed. The microwave-assisted Friedel-Crafts benzoylation results in good yields within short reaction times. Bismuth...

Molecular dynamics modeling the synthetic and biological polymers interactions pre-studied via docking: anchors modified polyanions interference with the HIV-1 fusion mediator.

Science.gov (United States)

Tsvetkov, Vladimir B; Serbin, Alexander V

2014-06-01

In previous works we reported the design, synthesis and in vitro evaluations of synthetic anionic polymers modified by alicyclic pendant groups (hydrophobic anchors), as a novel class of inhibitors of the human immunodeficiency virus type 1 (HIV-1) entry into human cells. Recently, these synthetic polymers interactions with key mediator of HIV-1 entry-fusion, the tri-helix core of the first heptad repeat regions [HR1]3 of viral envelope protein gp41, were pre-studied via docking in terms of newly formulated algorithm for stepwise approximation from fragments of polymeric backbone and side-group models toward real polymeric chains. In the present article the docking results were verified under molecular dynamics (MD) modeling. In contrast with limited capabilities of the docking, the MD allowed of using much more large models of the polymeric ligands, considering flexibility of both ligand and target simultaneously. Among the synthesized polymers the dinorbornen anchors containing alternating copolymers of maleic acid were selected as the most representative ligands (possessing the top anti-HIV activity in vitro in correlation with the highest binding energy in the docking). To verify the probability of binding of the polymers with the [HR1]3 in the sites defined via docking, various starting positions of polymer chains were tried. The MD simulations confirmed the main docking-predicted priority for binding sites, and possibilities for axial and belting modes of the ligands-target interactions. Some newly MD-discovered aspects of the ligand's backbone and anchor units dynamic cooperation in binding the viral target clarify mechanisms of the synthetic polymers anti-HIV activity and drug resistance prevention.

Organic chemistry of graphene: the Diels-Alder reaction.

Science.gov (United States)

Denis, Pablo A

2013-11-11

Herein, by using dispersion-corrected density functional theory, we investigated the Diels-Alder chemistry of pristine and defective graphene. Three dienes were considered, namely 2,3-dimethoxy-1,3-butadiene (DMBD), 9-methylanthracene (9MA), and 9,10-dimethylanthracene (910DMA). The dienophiles that were assayed were tetracyanoethylene (TCNE) and maleic anhydride (MA). When pristine graphene acted as the dienophile, we found that the cycloaddition products were 47-63 kcal mol(-1) less stable than the reactants, thus making the reaction very difficult. The presence of Stone-Wales translocations, 585 double vacancies, or 555-777 reconstructed double vacancies did not significantly improve the reactivity because the cycloaddition products were still located at higher energy than the reactants. However, for the addition of 910DMA to single vacancies, the product showed comparable stability to the separated reactants, whereas for unsaturated armchair edges the reaction was extremely favorable. With regards the reactions with dienophiles, for TCNE, the cycloaddition product was metastable. In the case of MA, we observed a reaction product that was less stable than the reactants by 50 kcal mol(-1) . For the reactions between graphene as a diene and the dienophiles, we found that the most-promising defects were single vacancies and unsaturated armchair edges, because the other three defects were much-less reactive. Thus, we conclude that the reactions with these above-mentioned dienes may proceed on pristine or defective sheets with heating, despite being endergonic. The same statement also applies to the dienophile maleic anhydride. However, for TCNE, the reaction is only likely to occur onto single vacancies or unsaturated armchair edges. We conclude that the dienophile character of graphene is slightly stronger than its behavior as a diene. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Determinacion de la configuracion E-Z de los acidos Fumarico y Maleico. Un experimento orientado a incentivar el desarrollo de la investigacion cientifica en alumnos de Pregrado Determination of the E-Z fumaric and maleic acids configuration. An experiment designed to develop scientific research abilities in undergraduates students

Directory of Open Access Journals (Sweden)

Carlos Bustos

2000-08-01

Full Text Available In this work we intend to eliminate the idea that laboratory exercises seem like cookbooks. That is, exercises shall be presented as a problematic situation. Based on observation and experimentation, the students should determine the E-Z configuration of maleic and fumaric acids. The basis of this laboratory exercise is the acid-catalyzed isomerization of maleic acid to fumaric acid. Students are given the starting material, reagents and the experimental procedure. They are told that the starting material is a dicarboxylic acid containing a C=C double bond of formula C4H4O4. Students determine melting points, solubilities, acidity and chromatographic patterns for both the starting material and the product, so that a configuration of each acid can be proposed. This type of experiment yields excellent results, because the students are left to deduce that maleic acid is less stable than fumaric acid. Additionally, they conclude that maleic acid is the "Z" isomer and fumaric acid is the "E" isomer. Finally, this laboratory exercise allows the students to develop simultaneously their critical-thinking skills with the respective laboratory techniques and not to see chemistry as recipes to be followed.

PP/clay nanocomposite films for food package; Filmes de nanocomposito PP/argila organofilica para embalagens de alimentos

Energy Technology Data Exchange (ETDEWEB)

Araujo, Arthur R.A.; Silva, Suedina M.L., E-mail: suedina@dema.ufcg.ed [Universidade Federal de Campina Grande (UAEMat/UFCG), PB (Brazil). Unidade Academica de Engenharia de Materiais; Andrade, Daniela L.A.C.S. [Universidade Federal de Campina Grande (UFCG), PB (Brazil). Programa de Pos-Graduacao em Engenharia de Processos; Mesquita, Wandemberg B [Felinto Industria e Comercio Ltda., Campina Grande, PB (Brazil)

2009-07-01

Small contents of organoclays (1 wt %) were incorporated to PP modified with maleic anhydride by melt intercalation, in order to prepare polymeric films for further applications in food package sector. The films were characterized by X-ray diffraction (XRD) and mechanical properties. The data indicates that the incorporation of organoclay to PP results in transparent films with intercalated morphology and highly. The mechanical properties of nanocomposites films were superior from those pristine films. The results evidences that the PP/PP-g-MA/organoclay nanocomposite films, prepared in this study might be promissory to the food package market and, in short time, be used like a new product by industries of this sector. (author)

Evaluation of the acquirement of nano composites of polypropylene and a bentonite organophilized by different methodologies

International Nuclear Information System (INIS)

Paiva, Lucilene B. de; Morales, Ana R.; Branciforti, Marcia C.; Bretas, Rosario E.S.

2009-01-01

This work describes the organophilization of an argentinean sodium bentonite with a quaternary ammo nium salt, by two methodologies: cation exchange in aqueous dispersion and intercalation in semi-solid medium. The modified samples were used in the preparation of nano composites, with polypropylene as a matrix and polypropylene-graft-maleic anhydride as a coupling agent, through melt intercalation by using a twin-screw micro extruder. The organophilic bentonites were characterized by the swelling capacity test in water and in xylene and by X-ray diffraction, and the nano composites were characterized by X-ray diffraction and transmission electronic microscopy. The results showed that were obtained nano composites with structures partially intercalated and exfoliated. (author)

Blending protocol effect in structural properties of PA6/ABS nanocomposites compatibilized with SAN-MA

International Nuclear Information System (INIS)

Castro, Lucas D.C. de; Oliveira, Amanda D.; Pessan, Luiz Antonio

2015-01-01

Nanocomposites based on polyamide 6 (PA6) and acrylonitrile-butadiene-styrene (ABS) compatibilized with styrene acrylonitrile-co-maleic anhydride were prepared using different blending protocols in a twin screw extruder. Specimen were prepared though injection molding. The organoclay (OMMT) incorporation and blending sequence effect on structural properties were investigated. X-ray diffraction analysis (XRD) indicates a complete exfoliated structure for all samples. Rheological measurements show an increasing in nanocomposites complex viscosities and storage modulus values when compared with the ternary blend. However, no significant effects in the rheological behavior were observed due the blending sequence. Differential scanning calorimetry (DSC) measurements suggests the incorporation of OMMT and different blending protocols may influence the polyamide polymorphism and degree of crystallinity. (author)

Thermo oxidative degradation of HMSPP/clay nanocomposite

International Nuclear Information System (INIS)

Komatsu, Luiz G.H.; Oliani, Washington L.; Lugao, Ademar B.; Parra, Duclerc F.

2013-01-01

The objective of this study was evaluate the effects of thermal ageing in dumbbell samples of nano composites using stove at 110 deg C, with air circulation at different periods of time. The clay, Cloisite 20 A, was added to HMSPP to obtain nano composites in proportion of 5 and 10 wt%. The nano composites were processed in twin screw extruder to compatibilizer the HMSPP (high melt strength polypropylene), polypropylene graft maleic anhydride (PP-g-MA) and the Cloisite 20 A The effects were evaluated by carbonyl index determination (CI), Fourier transformed infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), scanning electron microscopy (SEM). The nano composites showed intense cracks and yellowing after thermal ageing. (author)

Sulfated cellulose thin films with antithrombin affinity

Directory of Open Access Journals (Sweden)

2009-11-01

Full Text Available Cellulose thin films were chemically modified by in situ sulfation to produce surfaces with anticoagulant characteristics. Two celluloses differing in their degree of polymerization (DP: CEL I (DP 215–240 and CEL II (DP 1300–1400 were tethered to maleic anhydride copolymer (MA layers and subsequently exposed to SO3•NMe3 solutions at elevated temperature. The impact of the resulting sulfation on the physicochemical properties of the cellulose films was investigated with respect to film thickness, atomic composition, wettability and roughness. The sulfation was optimized to gain a maximal surface concentration of sulfate groups. The scavenging of antithrombin (AT by the surfaces was determined to conclude on their potential anticoagulant properties.

Blending protocol effect in structural properties of PA6/ABS nanocomposites compatibilized with SAN-MA; Influencia do protocolo de mistura nas propriedades estruturais de nanocompositos PA6/ABS compatibilizados com SAN-MA

Energy Technology Data Exchange (ETDEWEB)

Castro, Lucas D.C. de; Oliveira, Amanda D.; Pessan, Luiz Antonio, E-mail: lucasdanielcastro@hotmail.com, E-mail: pessan@ufscar.br [Universidade Federal de Sao Carlos (UFSCar), Sao Carlos, SP (Brazil). Programa de Pos-Graduacao em Ciencia e Engenharia de Materiais

2015-07-01

Nanocomposites based on polyamide 6 (PA6) and acrylonitrile-butadiene-styrene (ABS) compatibilized with styrene acrylonitrile-co-maleic anhydride were prepared using different blending protocols in a twin screw extruder. Specimen were prepared though injection molding. The organoclay (OMMT) incorporation and blending sequence effect on structural properties were investigated. X-ray diffraction analysis (XRD) indicates a complete exfoliated structure for all samples. Rheological measurements show an increasing in nanocomposites complex viscosities and storage modulus values when compared with the ternary blend. However, no significant effects in the rheological behavior were observed due the blending sequence. Differential scanning calorimetry (DSC) measurements suggests the incorporation of OMMT and different blending protocols may influence the polyamide polymorphism and degree of crystallinity. (author)

PP/clay nanocomposite films for food package

International Nuclear Information System (INIS)

Araujo, Arthur R.A.; Silva, Suedina M.L.

2009-01-01

Small contents of organoclays (1 wt %) were incorporated to PP modified with maleic anhydride by melt intercalation, in order to prepare polymeric films for further applications in food package sector. The films were characterized by X-ray diffraction (XRD) and mechanical properties. The data indicates that the incorporation of organoclay to PP results in transparent films with intercalated morphology and highly. The mechanical properties of nanocomposites films were superior from those pristine films. The results evidences that the PP/PP-g-MA/organoclay nanocomposite films, prepared in this study might be promissory to the food package market and, in short time, be used like a new product by industries of this sector. (author)

Nanocomposites of polypropylene and organophilic clay: X ray diffraction, absorption infrared spectroscopy with fourier transform and water vapor permeation

International Nuclear Information System (INIS)

Morelli, Fernanda C.; Ruvolo Filho, Adhemar

2010-01-01

In this work nano composites were prepared from polypropylene, graft polypropylene with maleic anhydride as compatibilizer and organophilic montmorillonite Cloisite 20A with concentrations of 1.5, 2.5, 5.0 and 7.5% clay. The mixture was made in the melt state using a twin screw extruder. The materials were characterized by X ray diffraction, infrared spectroscopy with Fourier transform and analysis of water vapor permeation. The results of X ray diffraction and absorption infrared spectroscopy indicates the formation of nano composites with structures probably exfoliate and or intercalated for concentrations of 1.5 and 2.5% clay, and provided a marked decrease in the water permeability, corroborating with other analyses. (author)

Ultrasonic-assisted preparation of graphene oxide carboxylic acid polyvinyl alcohol polymer film and studies of thermal stability and surface resistivity.

Science.gov (United States)

Li, Yongshen; Li, Jihui; Li, Yuehai; Li, Yali; Song, Yunan; Niu, Shuai; Li, Ning

2018-01-01

In this paper, flake graphite, nitric acid and acetic anhydride are used to prepare graphene oxide carboxylic acid (GO-COOH) via an ultrasonic-assisted method, and GO-COOH and polyvinyl alcohol polymer (PVA) are used to synthesize graphene oxide carboxylic acid polyvinyl alcohol polymer (GO-COOPVA) via the ultrasonic-assisted method, and GO-COOPVA is used to manufacture graphene oxide carboxylic acid polyvinyl alcohol polymer film (GO-COOPVA film) via a solidification method, and the structure and morphology of GO-COOH, GO-COOPVA and GO-COOPVA film are characterized, and the thermal stability and surface resistivity are measured in the case of the different amount of GO-COOH. Based on the characterization and measurement, it has been successively confirmed and attested that carboxyl groups implant on 2D lattice of GO to form GO-COOH, and GO-COOH and PVA have the esterification reaction to produce GO-COOPVA, and GO-COOPVA consists of 2D lattice of GO-COOH and the chain of PVA connected in the form of carboxylic ester, and GO-COOPVA film is composed of GO-COOPVA, and the thermal stability of GO-COOPVA film obviously improves in comparison with PVA film, and the surface resistivity of GO-COOPVA film clearly decreases. Copyright © 2017 Elsevier B.V. All rights reserved.

Mechanical properties of composites based on unsaturated polyester resins obtained by chemical recycling of poly(ethylene terephthalate

Directory of Open Access Journals (Sweden)

Marinković Aleksandar D.

2013-01-01

Full Text Available Composites based on unsaturated polyester (UPe resins and fumed silica AEROSIL® RY 50, NY 50, RX 50 and NAX 50, as well as graphite, TiO2 or organically modified clay CLOISITE 30B were prepared in order to investigate the influence of reinforcing agents on the mechanical properties of composites. Unsaturated polyester resins were synthesized from maleic anhydride and products of glycolysis, obtained by depolymerization of poly(ethylene terephthalate with dipropylene glycol (UPe1 resin and triethylene glycol (UPe2 resin in the presence of tetrabutyl titanate catalyst. The obtained unsaturated polyesters were characterized by FTIR spectroscopy, acid and hydroxyl values, and their mechanical properties were also examined. Significant increase of the tensile modulus, tensile strength and decrease of the elongation at break was observed for composites prepared after addition of 10 wt.% of graphite or 10 wt.% of TiO2 to the UPe resins, indicating strong interaction between matrix and filler particles. On the other hand, nanocomposites prepared using UPe2 and hydrophobically modified silica nanoparticles showed lower tensile strength and tensile modulus than polymer matrix. The presence of CLOISITE 30B had no significant influence on the mechanical properties of UPe1, while tensile strength and tensile modulus of UPe2 increased after adding 10 wt.% of clay. [Projekat Ministarstva nauke Republike Srbije, br. 172013

Adjuvant effect of Gantrez®AN nanoparticles during oral vaccination of piglets against F4+enterotoxigenic Escherichia coli.

Science.gov (United States)

Vandamme, Katrien; Melkebeek, Vesna; Vesna, Melkebeek; Cox, Eric; Eric, Cox; Remon, Jean Paul; Paul, Remon Jean; Vervaet, Chris; Chris, Vervaet

2011-02-15

In this study, the adjuvanticity of methylvinylether-co-maleic anhydride (Gantrez(®)AN) nanoparticles (NP) was investigated in an oral immunisation experiment of pigs against F4+enterotoxigenic Escherichia coli (F4+ETEC). In addition, Wheat Germ Agglutinin (WGA)-coating of the nanoparticles was tested for enterocyte-targeting. Pigs were either vaccinated with F4 fimbriae, F4 encapsulated in Gantrez(®)AN NP, F4 encapsulated in Gantrez(®)AN NP coated with WGA or F4 fimbriae mixed with empty Gantrez(®)AN NP. Only vaccination with the combination of F4 mixed with empty Gantrez(®)AN NP improved protection against F4+ETEC infection. In addition, vaccination with this formulation also resulted in an F4-specific serum antibody response prior to F4+ETEC challenge. Encapsulation of F4 in Gantrez(®)AN NP only raised the serum antibody response after F4+ETEC challenge compared to soluble F4, but did not improve protection, whereas WGA-coating almost completely abolished the serum antibody response. These data indicate that nanoparticle effects after F4 encapsulation were of lesser importance for the adjuvant effect of Gantrez(®)AN NP, contrarily to the reactivity of the Gantrez(®)AN polymer used to prepare the nanoparticles. Copyright © 2010 Elsevier B.V. All rights reserved.

Reaction of N-acetylneuraminic acid derivatives with perfluorinated anhydrides: a short access to N-perfluoracylated glycals with antiviral properties.

Science.gov (United States)

Rota, Paola; Allevi, Pietro; Mattina, Roberto; Anastasia, Mario

2010-08-21

An efficient short protocol for the preparation of N-perfluoroacylated glycals of neuraminic acid, by simple short treatment of differently protected N-acetylneuraminic acid with perfluorinated anhydrides in acetonitrile at 135 degrees C, is reported, together with a rationalitazion of the reaction that allows the alternative formation of N-perfluoroacylated 1,7-lactones to be previewed under the same reaction conditions.

Synthesis and characterization of triglyceride based thermosetting polymers

Science.gov (United States)

Can, Erde

2005-07-01

Plant oils, which are found in abundance in all parts of the world and are easily replenished annually, have the potential to replace petroleum as a chemical feedstock for making polymers. Within the past few years, there has been growing interest to use triglycerides as the basic constituent of thermosetting polymers with the necessary rigidity, strength and glass transition temperatures required for engineering applications. Plant oils are not polymerizable in their natural form, however various functional groups that can polymerize can easily be attached to the triglyceride structure making them ideal cross-linking monomers for thermosetting liquid molding resins. Through this research project a number of thermosetting liquid molding resins based on soybean and castor oil, which is a specialty oil with hydroxyls on its fatty acids, have been developed. The triglyceride based monomers were prepared via the malination of the alcoholysis products of soybean and castor oil with various polyols, such as pentaerythritol, glycerol, and Bisphenol A propoxylate. The malinated glycerides were then cured in the presence of a reactive diluent, such as styrene, to form rigid glassy materials with a wide range of properties. In addition to maleate half-esters, methacrylates were also introduced to the glyceride structure via methacrylation of the soybean oil glycerolysis product with methacrylic anhydride. This product, which contains methacrylic acid as by-product, and its blends with styrene also gave rigid materials when cured. The triglyceride based monomers were characterized via conventional spectroscopic techniques. Time resolved FTIR analysis was used to determine the curing kinetics and the final conversions of polymerization of the malinated glyceride-styrene blends. Dynamic Mechanical Analysis (DMA) was used to determine the thermomechanical behavior of these polymers and other mechanical properties were determined via standard mechanical tests. The use of lignin

Synthesis and characterization of poly(vinylphosphonic acid) for proton exchange membranes in fuel cells

Energy Technology Data Exchange (ETDEWEB)

Bingoel, Bahar

2007-07-01

Vinylphosphonic acid (VPA) was polymerized at 80 C by free radical polymerization to give polymers (PVPA) of different molecular weight depending on the initiator concentration. The highest molecular weight, Mw, achieved was 6.2 x 10{sup 4} g/mol as determined by static light scattering. High resolution nuclear magnetic resonance (NMR) spectroscopy was used to gain microstructure information about the polymer chain. Information based on tetrad probabilities was utilized to deduce an almost atactic configuration. In addition, {sup 13}CNMR gave evidence for the presence of head-head and tail-tail links. Refined analysis of the {sup 1}H NMR spectra allowed for the quantitative determination of the fraction of these links (23.5 percent of all links). Experimental evidence suggested that the polymerization proceeded via cyclopolymerization of the vinylphosphonic acid anhydride as an intermediate. Titration curves indicated that high molecular weight poly(vinylphosphonic acid) PVPA behaved as a monoprotic acid. Proton conductors with phosphonic acid moieties as protogenic groups are promising due to their high charge carrier concentration, thermal stability, and oxidation resistivity. Blends and copolymers of PVPA have already been reported, but PVPA has not been characterized sufficiently with respect to its polymer properties. Therefore, we also studied the proton conductivity behaviour of a well-characterized PVPA. PVPA is a conductor; however, the conductivity depends strongly on the water content of the material. The phosphonic acid functionality in the resulting polymer, PVPA, undergoes condensation leading to the formation of phosphonic anhydride groups at elevated temperature. Anhydride formation was found to be temperature dependent by solid state NMR. Anhydride formation affects the proton conductivity to a large extent because not only the number of charge carriers but also the mobility of the charge carriers seems to change. (orig.)

Intracellular responsive dual delivery by endosomolytic polyplexes carrying DNA anchored porous silicon nanoparticles

DEFF Research Database (Denmark)

Shahbazi, Mohammad Ali; Almeida, Patrick Vingadas; Correia, Alexandra

2017-01-01

-alt-maleic acid)) and a cationic endosomolytic polymer (polyethyleneimine). This combined nanocomposite is successfully tested for the co-delivery of hydrophobic (sorafenib) or hydrophilic (calcein) molecules loaded within the porous core, and an imaging agent covalently integrated into the polyplex shell...

Modificación de Betún-Venezuela por reacción de Friedel y Crafts

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Blanco, Manuel

1987-03-01

Full Text Available In this work, a Venezuelan-bitumen of newtonian nature was modified by Friedel and Crafts reaction, changing it in new materials that present pseudoplastic characteristics, with very different properties from the original product. These new materials are harder and have less thermical susceptibility and allow us to use them in many applications such as paving and roofing. The modifications have been made with rubbers, PVC, phtalic anhydride, maleic anhydride, 1, 2-propyleneglycol, hexamethylenediisocyanate and toluylene-2,4-diisocyanate.

En el presente trabajo se modificó un betún-Venezuela, de naturaleza newtoniana, mediante reacción de Friedel y Crafts, transformándolo en unos nuevos materiales, ya de carácter pseudoplástico, con unas propiedades notablemente distintas a las del producto de partida. Los nuevos materiales son más duros y de menor susceptibilidad térmica, lo que los hace útiles para pavimentación e impermeabilización. Las modificaciones se han realizado con cauchos, policloruro de vinilo, anhídrido ftálico, anhídrido maléico, 1,2-propanodiol, hexametilendiisocianato y toluen-2,4-diisocianato.

Modification of (DGEBA epoxy resin with maleated depolymerised natural rubber

Directory of Open Access Journals (Sweden)

2008-04-01

Full Text Available In this work, diglycidyl ether of bisphenol A (DEGBA type epoxy resin has been modified with maleated depolymerised natural rubber (MDPR. MDPR was prepared by grafting maleic anhydride onto depolymerised natural rubber. MDPR has been characterized by Fourier transform infrared (FT-IR spectroscopy and nuclear magnetic resonance spectroscopy. MDPR was blended with epoxy resin at three different ratios (97/3, 98/2 and 99/1, by keeping the epoxy resin component as the major phase and maleated depolymerised natural rubber component as the minor phase. The reaction between the two blend components took place between the acid/anhydride group in the MDPR and the epoxide group of the epoxy resin. The proposed reaction schemes were supported by the FT-IR spectrum of the uncured Epoxy/MDPR blends. The neat epoxy resin and Epoxy/MDPR blends were cured by methylene dianiline (DDM at 100°C for three hours. Thermal, morphological and mechanical properties of the neat epoxy and the blends were investigated. Free volume studies of the cured, neat epoxy and Epoxy/MDPR blends were correlated with the morphological and mechanical properties of the same systems using Positron Annihilation Lifetime Studies.

One-pot synthesis of thermoplastic mixed paramylon esters using trifluoroacetic anhydride.

Science.gov (United States)

Shibakami, Motonari; Tsubouchi, Gen; Sohma, Mitsugu; Hayashi, Masahiro

2015-03-30

Mixed paramylon esters prepared from paramylon (a storage polysaccharide of Euglena), acetic acid, and a long-chain fatty acid by one-pot synthesis using trifluoroacetic anhydride as a promoter and solvent were shown to have thermoplasticity. Size exclusion chromatography indicated that the mixed paramylon esters had a weight average molecular weight of approximately 4.9-6.7×10(5). Thermal analysis showed that these esters were stable in terms of the glass transition temperature (>90°C) and 5% weight loss temperature (>320°C). The degree of substitution of the long alkyl chain group, a dominant factor determining thermoplasticity, was controlled by tuning the feed molar ratio of acetic acid and long-chain fatty acid to paramylon. These results implied that the one-pot synthesis is useful for preparing structurally-well defined thermoplastic mixed paramylon esters with high molecular weight. Copyright © 2014 Elsevier Ltd. All rights reserved.

Evaluation of genotoxic activity of maleic hydrazide, ethyl methane sulfonate, and N-nitroso diethylamine in Tradescantia.

Science.gov (United States)

Alvarez-Moya, C; Santerre-Lucas, A; Zúñiga-González, G; Torres-Bugarín, O; Padilla-Camberos, E; Feria-Velasco, A

2001-01-01

To assess the genotoxic activity of N-nitroso diethylamine (NDEA), maleic hydrazide (MH), and ethyl methane sulfonate (EMS) using two systems: the comet assay on nuclei from Tradescantia, and the pink mutation test on Tradescantia staminal hairs (clone 4430). Tradescantia cups was obtained from Laboratorio de Citogenética y Mutagénesis del Centro de Ciencias de la Atmósfera de la Universidad Nacional Autónoma de México and treated with: N-nitroso diethylamine (NDEA) at 1, 5, 10 mM, maleic hydrazide (MH) at 1, 5, 10 mM and ethyl methane sulfonate (EMS) at 15, 30 and 45 mM; and used in both pink mutation assay and comet assay using cellular nuclei from Tradescantia staminal hairs. The observation of staminal hair was realized along eight days (6-14) after treatment), flowers produced day 14 after treatment were utilized done according to Underbrink. In previous reports on plants, were comet assay was used, breaking cellular wall and separating by centrifugation gradient are necessary. Here, nuclei from staminal hairs were obtained by squashing the cells (is not necessary to utilize to break special procedure cellular wall), collected using a nylon mesh of 80 Mm and next the comet assay was applied. Student's T test was the statistical test used for analyzing the comet assay data. Both assays showed a great sensitivity to the studied mutagens. A relationship between the dose-pink event and the dose-tail length was evident. Even though the Tradescantia mutation assay is a sensitive test with MH and EMS, low doses of NDEA were not able to induce a significant increase in the pink event frequencies; however, the comet assay was able to detect the mutagenic effect of NDEA at the same dose. Thus, it is clear that the comet assay is highly sensitive to the lowest dose of chemical mutagens. The comet assay on nuclei from Tradescantia staminal hairs is a useful tool to monitor genotoxic agents; it is simple, highly sensitive, and faster than the pink mutation test.

Monosaccharide anhydrides, monocarboxylic acids and OC/EC in PM1 aerosols in urban areas in the Czech Republic

Czech Academy of Sciences Publication Activity Database

Křůmal, Kamil; Mikuška, Pavel; Večeřa, Zbyněk

2015-01-01

Roč. 6, č. 6 (2015), s. 917-927 ISSN 1309-1042 R&D Projects: GA MŽP SP/1A3/148/08; GA ČR(CZ) GBP503/12/G147; GA ČR GA13-01438S; GA ČR(CZ) GA14-25558S Institutional support: RVO:68081715 Keywords : Monosaccharide anhydrides * carboxylic acids * fatty acids * organic carbon * biomass burning Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 1.401, year: 2015

The Use of Maleic Hydrazide for Effective Hybridization of Setaria viridis.

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Govinda Rizal

Full Text Available An efficient method for crossing green foxtail (Setaria viridis is currently lacking. S. viridis is considered to be the new model plant for the study of C4 system in monocots and so an effective crossing protocol is urgently needed. S. viridis is a small grass with C4-NADP (ME type of photosynthesis and has the advantage of having small genome of about 515 Mb, small plant stature, short life cycle, multiple tillers, and profuse seed set, and hence is an ideal model species for research. The objectives of this project were to develop efficient methods of emasculation and pollination, and to speed up generation advancement. We assessed the response of S. viridis flowers to hot water treatment (48°C and to different concentrations of gibberellic acid, abscisic acid, maleic hydrazide (MH, and kinetin. We found that 500 μM of MH was effective in the emasculation of S. viridis, whilst still retaining the receptivity of the stigma to pollination. We also report effective ways to accelerate the breeding cycle of S. viridis for research through the germination of mature as well as immature seeds in optimized culture media. We believe these findings will be of great interest to researchers using Setaria.

Modification of polylactide bioplastic using hyperbranched polymer based nanostructures

Science.gov (United States)

Bhardwaj, Rahul

maximum average matrix ligament thickness was 114 nm for a toughened polylactide nanoblend and correlated well with the theoretical prediction of the matrix ligament thickness. Fourier transform infrared spectroscopy and dynamic mechanical thermal analysis proved the crosslinking of the HBP phase in the PLA matrix. The crosslinked HBP was effective at hydroxyl (-OH) to anhydride molar ratios of: 2:1, 1:1 or 1:2. The glass transition temperature values of the crosslinked HBP phase at these molar ratios were observed to deviate from the predictions made by the Fox equation. The hydrophilic nature of the hyperbranched polymer was altered to hydrophobic by incorporation of polyanhydride crosslinker, as demonstrated by the increase in the contact angle with water. Rheological studies showed that there was a network formation in the PLA matrix after in-situ crosslinking of HBP. The HBP was found to reduce the melt viscosity of PLA dramatically and this effect was maintained even after its in-situ crosslinking in the PLA matrix. Finally, the current research unwraps the new opportunities provided by the unique physical and chemical properties of highly functional hyperbranched polymers in generating new nanostructured multiphase polymer systems with enhanced properties.

In vivo conjugation of nasal lavage proteins by hexahydrophthalic anhydride

International Nuclear Information System (INIS)

Johannesson, Gunvor; Lindh, Christian; Nielsen, Joern; Bjoerk, Birgitta; Rosqvist, Seema; Joensson, Bo A.G.

2004-01-01

Hexahydrophthalic anhydride (HHPA), an industrially important chemical, is a highly allergenic compound. The aim of this work was to identify proteins in nasal lavage fluid (NLF) that form adducts with HHPA. Such bindings may induce production of specific immunoglobulin E (IgE) or affect physiological mechanisms of the proteins. NLF was obtained from HHPA-exposed volunteers, workers and exposed guinea pigs. HHPA-binding proteins were visualized with immunoblotting using a polyclonal antiserum against HHPA. The proteins were excised from sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) gels, digested with trypsin and identified by tandem mass spectrometry (MS/MS) and database searches. The antiserum was found to be specific for HHPA-bound proteins. In vivo formed HHPA-binding proteins in humans were identified as antileukoproteinase, immunoglobulin G (IgG), immunoglobulin A (IgA), serum albumin and lactoferrin. In addition, several proteins binding to HHPA were found in NLFs from guinea pigs but these could not be identified from database searches. Hypotheses for development of airways diseases by adduction of this allergenic compound to the NLF proteins in humans were established

Diastereoselective and one-pot synthesis of trans-isoquinolonic acids via three-component condensation of homophthalic anhydride, aldehydes, and ammonium acetate catalyzed by aspartic acid

Czech Academy of Sciences Publication Activity Database

Ghorbani-Choghamarani, A.; Hajjami, M.; Norouzi, M.; Abbasityula, Y.; Eigner, Václav; Dušek, Michal

2013-01-01

Roč. 69, č. 32 (2013), s. 6541-6544 ISSN 0040-4020 Grant - others:AVČR(CZ) Praemium Academiae Institutional support: RVO:68378271 Keywords : isoquinolonic acid * diastereoselective * aldehyde * homophthalic anhydride * ammonium acetate Subject RIV: CC - Organic Chemistry Impact factor: 2.817, year: 2013

The behaviour of tungsten electrodes in a mixture of acetic acid and acetic anhydride

International Nuclear Information System (INIS)

Pastor, T.J.; Vajgand, V.H.

1976-01-01

Tungsten electrodes have advantageously been used for potentiometric end-point detection in perchloric acid titration of bases in a mixture of acetic acid and acetic anhydride. They have also given good results in biamperometric detection of the equivalence point in continuous coulometric titration of small quantities of bases and acids in the same solvent. Tungsten electrodes in the presence of quinhydrone behave like platinum electrodes, but in biamperometric end-point determination in the absence of quinhydrone it is better to remove the oxide layer from their surface. Some other factors affecting their behaviour have also been studied. Errors in determination do not exceed +-2% even in titration of very small quantities of substances. (author)

EFFECT OF SUBSTITUTION POSITION OF HYDROXY GROUP AT BENZOIC ACID ON THE LUMINESCENT AND DEGRADATION PROPERTIES OF POLY[DI(CARBOXYPHENYL) SUCCINATE-co-SEBACIC ANHYDRIDE]S

Institute of Scientific and Technical Information of China (English)

Jun Fan; Hong-liang Jiang; Kang-jie Zhu

2007-01-01

In this work, two new diacids, di(m-carboxyphenyl) succinate (m-dCPS) and di(o-carboxyphenyl) succinate (o-dCPS), were synthesized by reaction of m-, o-hydroxy benzoic acid with succinic chloride, respectively. Their corresponding copolymers with sebacic acid (SA), P(m-dCPS:SA) and P(o-dCPS:SA), were prepared by melt copolycondensation and characterized by NMR, UV and DSC methods. Compared with inherently fluorescent poly[di(p-carboxyphenyl) succinateco-sebacic anhydride] (P(p-dCPS:SA)), P(m-dCPS:SA) and P(o-dCPS:SA) displayed different luminescent properties. P(m-dCPS:SA) could emit fluorescence under the excitation of both visible and UV light, while P(o-dCPS:SA) could only emit fluorescence when excited with UV light. Degradation rate of the two new copolyanhydrides increased with the increase of SA fraction in the copolymers. In addition, P(o-dCPS:SA) degraded more rapidly than P(m-dCPS:SA) with the same composition. Typical surface-degradation characteristics of these copolyanhydrides were observed.

Preparation of deuterated succinic acids

Energy Technology Data Exchange (ETDEWEB)

Tashiro, Masashi; Tsuzuki, Hirohisa; Goto, Hideyuki; Ogasahara, Shoji; Mataka, Shuntaro (Kyushu Univ., Fukuoka (Japan)); Isobe, Shin-ichiro; Yonemitsu, Tadashi (Kyushu Sangyo Univ., Fukuoka (Japan). Dept. of Industrial Chemistry)

1991-04-01

Succinic (2,3-{sup 2}H{sub 2})- and (2,2,3,3-{sup 2}H{sub 4})-acids were prepared from maleic anhydride and dimethyl fumarate, and acetylene dicarboxylic acid and its dimethyl ester by treatment with Cu-Al and Ni-Al alloys in 10% NaOD-D{sub 2}0 in 95% to 100% isotopic purity. The succinic {sup 2}H{sub 4} acid having high isotopic purity was also obtained on the hydrolysis of 1,2-ethanedinitrile with alkaline deuterium oxide. Based on the {sup 1}H({sup 2}H) spectra analysis of N-(o-biphenyl)(2,3-{sup 2}H{sub 2})succinimide, it was elucidated that the Raney alloy reduction with alkaline deuterium oxide proceeds stepwise. (author).

Reologi, sifat aging, termal, dan swelling dari campuran EPDM/NR dengan bahan pengisi carbon black N220

Directory of Open Access Journals (Sweden)

Arum Yuniari

2016-06-01

Full Text Available The blends of EPDM and NR are immiscible in nature and incompatible. Introducing maleic anhydride as a compatibilizer into the blends was expected to produce compatible blends with balanced mechanical properties. The purpose of this research was to determine the effect of EPDM/NR ratio on the rheological, aging, thermal and swelling properties of the blends. The variation of EPDM/NR ratio were 100/0, 80/20, 70/30, 60/40, 50/50, and 40/60 phr. The blends were mixed using two roll mill. The results showed that the addition of NR affects the maximum torque, scorch time, and optimum vulcanization time. In the blends, EPDM plays an important role in improving aging, swelling, thermal properties.

Novel composite sorbent AAm/MA hydrogels containing starch and ...

Indian Academy of Sciences (India)

A novel polymer/clay composite sorbent based on acrylamide/maleic acid, starch and clay such as kaolin was synthesized with free radical solution polymerization by using ammonium persulfate/,,','-tetramethylethylenediamine as redox initiating pair in the presence of poly(ethylene glycol)diacrylate as a crosslinker.

Curing behaviors and properties of an extrinsic toughened epoxy/anhydride system and an intrinsic toughened epoxy/anhydride system

International Nuclear Information System (INIS)

Fan, Mengjin; Liu, Jialin; Li, Xiangyuan; Cheng, Jue; Zhang, Junying

2013-01-01

Highlights: ► Two curing systems (ETRS and ITRS) with similar chemical composite were prepared. ► The curing kinetics of the ETRS and the novel ITRS were comparatively studied. ► Crosslinking density can affect the kinetic schemes of the two curing systems. ► Their mechanical properties and thermal stabilities were also comparatively studied. ► Crosslinking density may play an influential role in mechanical properties. - Abstract: The curing kinetics of an extrinsic toughened epoxy (mixture of diglycidyl ether of bisphenol-A and 1,4-butanediol epoxy resin, DGEBA/DGEBD) and an intrinsic toughened epoxy (ethoxylated bisphenol-A epoxy resin with two oxyethylene units, DGEBAEO-2) using hexahydrophthalic anhydride (HHPA) as curing agent and tris-(dimethylaminomethyl) phenol (DMP-30) as accelerator were comparatively studied by non-isothermal DSC with a model-fitting Málek approach and a model-free advanced isoconversional method of Vyazovkin. The dynamic mechanical properties and thermal stabilities of the cured materials were investigated by DMTA and TGA, respectively. The results showed that Šesták–Berggren model can generally simulate well the reaction rates of these two systems. The activation energy of DGEBA/DGEBD/HHPA/DMP-30 at high fractional conversion changed much higher than that of DGEBAEO-2/HHPA/DMP-30, indicating the increased steric hindrance mainly affected the reaction kinetic scheme of DGEBA/DGEBD/HHPA/DMP-30. The T g and storage moduli of cured DGEBAEO-2/HHPA/DMP-30 were lower than those of cured DGEBA/DGEBD/HHPA/DMP-30 according to DMTA while TGA showed that the thermal stabilities of these two cured systems were similar

Curing behaviors and properties of an extrinsic toughened epoxy/anhydride system and an intrinsic toughened epoxy/anhydride system

Energy Technology Data Exchange (ETDEWEB)

Fan, Mengjin; Liu, Jialin; Li, Xiangyuan [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Cheng, Jue, E-mail: chengjue@mail.buct.edu.cn [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Zhang, Junying, E-mail: zjybuct@gmail.com [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China)

2013-02-20

Highlights: ► Two curing systems (ETRS and ITRS) with similar chemical composite were prepared. ► The curing kinetics of the ETRS and the novel ITRS were comparatively studied. ► Crosslinking density can affect the kinetic schemes of the two curing systems. ► Their mechanical properties and thermal stabilities were also comparatively studied. ► Crosslinking density may play an influential role in mechanical properties. - Abstract: The curing kinetics of an extrinsic toughened epoxy (mixture of diglycidyl ether of bisphenol-A and 1,4-butanediol epoxy resin, DGEBA/DGEBD) and an intrinsic toughened epoxy (ethoxylated bisphenol-A epoxy resin with two oxyethylene units, DGEBAEO-2) using hexahydrophthalic anhydride (HHPA) as curing agent and tris-(dimethylaminomethyl) phenol (DMP-30) as accelerator were comparatively studied by non-isothermal DSC with a model-fitting Málek approach and a model-free advanced isoconversional method of Vyazovkin. The dynamic mechanical properties and thermal stabilities of the cured materials were investigated by DMTA and TGA, respectively. The results showed that Šesták–Berggren model can generally simulate well the reaction rates of these two systems. The activation energy of DGEBA/DGEBD/HHPA/DMP-30 at high fractional conversion changed much higher than that of DGEBAEO-2/HHPA/DMP-30, indicating the increased steric hindrance mainly affected the reaction kinetic scheme of DGEBA/DGEBD/HHPA/DMP-30. The T{sub g} and storage moduli of cured DGEBAEO-2/HHPA/DMP-30 were lower than those of cured DGEBA/DGEBD/HHPA/DMP-30 according to DMTA while TGA showed that the thermal stabilities of these two cured systems were similar.

Application of Nanoparticle Technology to Reduce the Anti-Microbial Resistance through β-Lactam Antibiotic-Polymer Inclusion Nano-Complex.

Science.gov (United States)

Salamanca, Constain H; Yarce, Cristhian J; Roman, Yony; Davalos, Andrés F; Rivera, Gustavo R

2018-02-10

Biocompatible polymeric materials with potential to form functional structures in association with different therapeutic molecules have a high potential for biological, medical and pharmaceutical applications. Therefore, the capability of the inclusion of nano-Complex formed between the sodium salt of poly(maleic acid- alt -octadecene) and a β-lactam drug (ampicillin trihydrate) to avoid the chemical and enzymatic degradation and enhance the biological activity were evaluated. PAM-18Na was produced and characterized, as reported previously. The formation of polymeric hydrophobic aggregates in aqueous solution was determined, using pyrene as a fluorescent probe. Furthermore, the formation of polymer-drug nano-complexes was characterized by Differential Scanning Calorimetry-DSC, viscometric, ultrafiltration/centrifugation assays, zeta potential and size measurements were determined by dynamic light scattering-DLS. The PAM-18Na capacity to avoid the chemical degradation was studied through stress stability tests. The enzymatic degradation was evaluated from a pure β-lactamase, while the biological degradation was determined by different β-lactamase producing Staphylococcus aureus strains. When ampicillin was associated with PAM-18Na, the half-life time in acidic conditions increased, whereas both the enzymatic degradation and the minimum inhibitory concentration decreased to a 90 and 75%, respectively. These results suggest a promissory capability of this polymer to protect the β-lactam drugs against chemical, enzymatic and biological degradation.

Development of wet-dry reversible reverse osmosis membrane with high performance from cellulose acetate and cellulose triactate blend

NARCIS (Netherlands)

Vasarhelyi, K.; Ronner, J.A.; Mulder, M.H.V.; Smolders, C.A.

1987-01-01

Wet-dry reversible membrane were prepared bt a two-step coagulation procedure. A cast film containing a blend of cellulose triacetate as polymers, dioxane and acetone as solvents and maleic acid and methanol as additives was immersed consecutively in two aqueous coagulation baths, the first bath

Surface Functionalization of WO3 Thin Films with (3-Aminopropyl)triethoxysilane and Succinic Anhydride

Science.gov (United States)

Ta, Thi Kieu Hanh; Tran, Thi Nhu Hoa; Tran, Quang Minh Nhat; Pham, Duy Phong; Pham, Kim Ngoc; Cao, Thi Thanh; Kim, Yong Soo; Tran, Dai Lam; Ju, Heongkyu; Phan, Bach Thang

2017-06-01

We report effects of oxygen plasma treatment on the surface functionalization of WO3 thin films with (3-aminopropyl)triethoxysilane (APTES) and succinic anhydride (SA). X-ray diffraction and x-ray photoelectron spectroscopy results indicate the existence of the WO3 phase. Fourier transform infrared spectroscopy measurement shows clear bands at 1040 cm-1 (Si-O-Si), 1556 cm-1 (N-H), 1655 cm-1 (C=O), 2937 cm-1 (C-H) and 3298 cm-1 (N-H), confirming the surface functionalization efficiency enhanced by prior treatment of oxygen plasma. It thus follows that the prior oxygen plasma treatment activates hydroxylation with more -OH groups on the WO3 surface, which can pave a highly efficient way to the surface functionalization by APTES and SA.

Poly(imide benzimidazole)s for high temperature polymer electrolyte membrane fuel cells

DEFF Research Database (Denmark)

Yuan, Sen; Guo, Xiaoxia; Aili, David

2014-01-01

A series of poly(imide benzimidazole) random copolymers (PIBIs) was synthesized by condensation polymerization of biphenyl-4,4'-diyldi(oxo)-4,4'-bis(1,8-naphthalenedicarboxylic anhydride) (BPNDA), 2-(4-aminophenyl)-5-aminobenzimidazole (APABI) and 4,4'diaminodiphenyl ether (ODA) in m-cresol in th......A series of poly(imide benzimidazole) random copolymers (PIBIs) was synthesized by condensation polymerization of biphenyl-4,4'-diyldi(oxo)-4,4'-bis(1,8-naphthalenedicarboxylic anhydride) (BPNDA), 2-(4-aminophenyl)-5-aminobenzimidazole (APABI) and 4,4'diaminodiphenyl ether (ODA) in m...

Evaluation of genotoxic activity of maleic hydrazide, ethyl methane sulfonate, and N-nitroso diethylamine in Tradescantia

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Alvarez-Moya Carlos

2001-01-01

Full Text Available Objective. To assess the genotoxic activity of N-nitroso diethylamine (NDEA, maleic hydrazide (MH, and ethyl methane sulfonate (EMS using two systems: the comet assay on nuclei from Tradescantia, and the pink mutation test on Tradescantia staminal hairs (clone 4430. Material and Methods. Tradescantia cups was obtained from Laboratorio de Citogenética y Mutagénesis del Centro de Ciencias de la Atmósfera de la Universidad Nacional Autónoma de México and treated with: N-nitroso diethylamine (NDEA at 1, 5, 10 mM, maleic hidrazide (MH at 1, 5, 10 mM and ethyl methane sulfonate (EMS at 15, 30 and 45 mM; and used in both pink mutation assay and comet assay using cellular nuclei from Tradescantia staminal hairs. The observation of staminal hair was realized along eight days (6-14 after treatment, flowers produced day 14 after treatment were utilized done according to Underbrink. In previous reports on plants, were comet assay was used, breaking cellular wall and separating by centrifugation gradient are necessary. Here, nuclei from staminal hairs were obtained by squashing the cells (is not necessary to utilize to break special procedure cellular wall, collected using a nylon mesh of 80Mm and next the comet assay was applied. Student's T test was the statistical test used for analyzing the comet assay data. Results. Both assays showed a great sensitivity to the studied mutagens. A relationship between the dose-pink event and the dose-tail length was evident. Even though the Tradescantia mutation assay is a sensitive test with MH and EMS, low doses of NDEA were not able to induce a significant increase in the pink event frequencies; however, the comet assay was able to detect the mutagenic effect of NDEA at the same dose. Thus, it is clear that the comet assay is highly sensitive to the lowest dose of chemical mutagens. Conclusions. The comet assay on nuclei from Tradescantia staminal hairs is a useful tool to monitor genotoxic agents; it is simple

Solubilization of human cells by the styrene-maleic acid copolymer: Insights from fluorescence microscopy.

Science.gov (United States)

Dörr, Jonas M; van Coevorden-Hameete, Marleen H; Hoogenraad, Casper C; Killian, J Antoinette

2017-11-01

Extracting membrane proteins from biological membranes by styrene-maleic acid copolymers (SMAs) in the form of nanodiscs has developed into a powerful tool in membrane research. However, the mode of action of membrane (protein) solubilization in a cellular context is still poorly understood and potential specificity for cellular compartments has not been investigated. Here, we use fluorescence microscopy to visualize the process of SMA solubilization of human cells, exemplified by the immortalized human HeLa cell line. Using fluorescent protein fusion constructs that mark distinct subcellular compartments, we found that SMA solubilizes membranes in a concentration-dependent multi-stage process. While all major intracellular compartments were affected without a strong preference, plasma membrane solubilization was found to be generally slower than the solubilization of organelle membranes. Interestingly, some plasma membrane-localized proteins were more resistant against solubilization than others, which might be explained by their presence in specific membrane domains with differing properties. Our results support the general applicability of SMA for the isolation of membrane proteins from different types of (sub)cellular membranes. Copyright © 2017 Elsevier B.V. All rights reserved.

The Mechanical Properties of Recycled Polyethylene-Polyethylene Terephthalate Composites

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Ehsan Avazverdi

2015-02-01

Full Text Available Polyethylene terephthalate (PET, one of the thermoplastic polymers, is encountered with arduous problems in its recycling. After recycling, its mechanical properties drop dramatically and therefore it cannot be used to produce the products as virgin PET does. Polyethylene is a thermoplastic polymer which can be easily recycled using the conventional recycling processes. The decreased mechanical properties of virgin polyethylene due to the environmental factors can be improved by reinforcing fillers. In this paper, we studied the effects of adding recycled polyethylene terephthalate (rPET as a filler, in various amounts with different sizes, on the physical and mechanical properties of recycled polyethylene. Composite samples were prepared using an internal mixer at temperature 185°C, well below rPET melting point (250°C, and characterized by their mechanical properties. To improve the compatibility between different components, PE grafted with maleic anhydride was added as a coupling agent in all the compositions under study. The mechanical properties of the prepared samples were performed using the tensile strength, impact strength, surface hardness and melt flow index (MFI tests. To check the dispersity of the polyethylene terephthalate powder in the polyethylene matrix, light microscopy was used. The results showed that the addition of rPET improved the tensile energy, tensile modulus and surface hardness of the composites while reduced the melt flow index, elongation-at-yield, tensile strength and fracture energy of impact test. We could conclude that with increasing rPET percentage in the recycled polyethylene matrix, the composite became brittle, in other words it decreased the plastic behavior of recycled polyethylene. Decreasing particle size led to higher surface contacts, increased the mechanical properties and made the composite more brittle. The light microscopy micrographs of the samples showed a good distribution of small r

Blendas de poliamida 6/elastômero: propriedades e influência da adição de agente compatibilizante Polyamide 6/elastomer blends: properties and compatibilizer influence

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Guilherme M. O. Barra

2003-06-01

Full Text Available Neste trabalho foram estudadas as propriedades micro e macroscópicas de misturas físicas binárias de poliamida 6 [PA6] com copolímero poli(etileno-co-propileno-co-dieno [EPDM] e em presença de pequenas quantidades de EPDM ou EPM enxertados com anidrido maleico, atuando como agentes compatibilizantes. Os componentes puros (poliamida 6 e EPDM e as blendas poliméricas em diferentes composições foram analisados por calorimetria diferencial de varredura (DSC e espectroscopia de infravermelho (FTIR. Os resultados indicaram a imiscibilidade dos componentes da mistura em toda a faixa de composição estudada. A utilização das técnicas de análise elementar, microscopia eletrônica de varredura e propriedades mecânicas permitiu avaliar a homogeneidade da mistura, a redução do tamanho dos domínios do elastômero e o aumento da força de impacto da matriz de PA6 com a adição do agente compatibilizante à mistura binária de PA6/EPDM.This study describes the micro- and macroscopic properties of polyamide 6 (PA6 and ethylene /propylene/diene copolymer (EPDM blends, and the effects from small quantities of EPDM or EPM grafted with maleic anhydride in this polymer mixture. The components and polymer blends at different compositions were analyzed by differential scanning calorimeter (DSC and infrared spectroscopy (FTIR. The results suggest immiscible mixture in all ranges of the blend's compositions. Scanning electron microscopy (SEM micrographs of the blends indicated that the size of rubber aggregates decreases as the functionalized elastomer (EPDM-g-MA or EPM-g-MA is added to the PA6/EPDM mixture, and the impact strength of the PA6 matrix increases significantly.

Copper(II) sulfate pentahydrate (CuSO4.5H2O): a green catalyst for solventless acetylation of alcohols and phenols with acetic anhydride

OpenAIRE

Heravi,Majid M.; Behbahani,Farahnaz K.; Zadsirjan,Vahideh; Oskooie,Hossien A.

2006-01-01

Alcohols and phenols were efficiently acetylated with acetic anhydride in the presence of copper (II) sulfate at room temperature in high yields. Álcoois e fenóis foram acetilados eficientemente com anidrido acético na presença de sulfato de cobre (II) em temperatura ambiente, com altos rendimentos.

Natural fibers for hydrogels production and their applications in agriculture

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Liliana Serna Cock

2017-10-01

Full Text Available This paper presents a review on hydrogels applied to agriculture emphasizing on the use of natural fibers. The objectives were to examine, trends in research addressed to identify natural fibers used in hydrogels development and methods for modifying natural fibers, understand factors which determine the water retention capacity of a hydrogel. Consequently, this paper shows some methodologies used to evaluate the hydrogels efficiency and to collect in tables, relevant information in relation to methods of natural fibers modification and hydrogel synthesis. It was found that previous research focused on hydrogels development processed with biodegradable polymers such as starch, chitosan and modified natural fibers, cross-linked with potassium acrylate and acrylamide, respectively. In addition, current researches aimed to obtaining hydrogels with improved properties, which have allowed a resistance to climatic variations and soil physicochemical changes, such as pH, presence of salts, temperature and composition. In fact, natural fibers such as sugarcane, agave fiber and kapok fiber, modified with maleic anhydride, are an alternative to obtain hydrogels due to an increasing of mechanical properties and chemically active sites. However, the use of natural nanofibers in hydrogels, has been a successful proposal to improve hydrogels mechanical and swelling properties, since they give to material an elasticity and rigidity properties. A hydrogel efficiency applied to soil, is measured throughout properties as swellability, mechanical strength, and soil water retention. It was concluded that hydrogels, are an alternative to the current needs for the agricultural sector.

Core-shell nanoparticles optical sensors - Rational design of zinc ions fluorescent nanoprobes of improved analytical performance

Science.gov (United States)

Woźnica, Emilia; Gasik, Joanna; Kłucińska, Katarzyna; Kisiel, Anna; Maksymiuk, Krzysztof; Michalska, Agata

2017-10-01

In this work the effect of affinity of an analyte to a receptor on the response of nanostructural fluorimetric probes is discussed. Core-shell nanoparticles sensors are prepared that benefit from the properties of the phases involved leading to improved analytical performance. The optical transduction system chosen is independent of pH, thus the change of sample pH can be used to control the analyte - receptor affinity through the "conditional" binding constant prevailing within the lipophilic phase. It is shown that by affecting the "conditional" binding constant the performance of the sensor can be fine-tuned. As expected, increase in "conditional" affinity of the ligand embedded in the lipophilic phase to the analyte results in higher sensitivity over narrow concentration range - bulk reaction and sigmoidal shape response of emission intensity vs. logarithm of concentration changes. To induce a linear dependence of emission intensity vs. logarithm of analyte concentration covering a broad concentration range, a spatial confinement of the reaction zone is proposed, and application of core-shell nanostructures. The core material, polypyrrole nanospheres, is effectively not permeable for the analyte - ligand complex, thus the reaction is limited to the outer shell layer of the polymer prepared from poly(maleic anhydride-alt-1-octadecene). For herein introduced system a linear dependence of emission intensity vs. logarithm of Zn2+ concentration was obtained within the range from 10-7 to 10-1 M.

Polycarbonate-Based Blends for Optical Non-linear Applications

Science.gov (United States)

Stanculescu, F.; Stanculescu, A.

2016-02-01

This paper presents some investigations on the optical and morphological properties of the polymer (matrix):monomer (inclusion) composite materials obtained from blends of bisphenol A polycarbonate and amidic monomers. For the preparation of the composite films, we have selected monomers characterised by a maleamic acid structure and synthesised them starting from maleic anhydride and aniline derivatives with -COOH, -NO2, -N(C2H5)2 functional groups attached to the benzene ring. The composite films have been deposited by spin coating using a mixture of two solutions, one containing the matrix and the other the inclusion, both components of the composite system being dissolved in the same solvent. The optical transmission and photoluminescence properties of the composite films have been investigated in correlation with the morphology of the films. The scanning electron microscopy and atomic force microscopy have revealed a non-uniform morphology characterised by the development of two distinct phases. We have also investigated the generation of some optical non-linear (ONL) phenomena in these composite systems. The composite films containing as inclusions monomers characterised by the presence of one -COOH or two -NO2 substituent groups to the aromatic nucleus have shown the most intense second-harmonic generation (SHG). The second-order optical non-linear coefficients have been evaluated for these films, and the effect of the laser power on the ONL behaviour of these materials has also been emphasised.

Urinary loss of glucose, phosphate, and protein by diffusion into proximal straight tubules injured by D-serine and maleic acid

International Nuclear Information System (INIS)

Carone, F.A.; Nakamura, S.; Goldman, B.

1985-01-01

In several models of acute renal failure leakage of glomerular filtrate out of the tubule is an important pathogenetic mechanism; however, bidirectional diffusion of solute to account for certain pathophysiologic features of acute renal failure has received meager attention. Using micropuncture and clearance methods, the authors assessed sequentially leakage of solutes and inulin across proximal straight tubules (PST) injured by two nephrotoxins. In d-serine-treated rats with extensive necrosis of PST, the basis for glucosuria and tubular leakage of inulin was studied. Glucose absorption by the proximal convoluted tubule and glucose delivery to the PST were normal, but glucose delivery to the distal tubule was increased nearly 8-fold, indicating diffusion of glucose from interstitial to tubular luminal fluid across the necrotic PST. Total kidney inulin clearance was greatly reduced, but single nephron glomerular filtration rate, based on proximal convoluted tubule samples, was normal, indicating tubular loss of inulin. Urinary recovery of [ 14 C]inulin infused into tubular lumina revealed that proximal convoluted tubule and distal tubule were impermeable to inulin and that inulin diffused out of the necrotic PST. The progressive return over 6 days of tubular impermeability for inulin correlated with relining of PST with new cells. In maleic acid-treated rats the site and extent of tubular necrosis and the nature of urinary loss of solutes were studied. Microdissection revealed that maleic acid caused limited necrosis of PST which averaged 7.4% of total proximal tubular length. Increased urinary excretion of protein, phosphate, and glucose and increased tubular permeability to microinfused [ 14 C]inulin occurred with the onset of PST necrosis, and return of these abnormalities to normal correlated with the degree of cellular repair of the PST

Bioconjugation of laminin peptide YIGSR with poly(styrene co-maleic acid) increases its antimetastatic effect on lung metastasis of B16-BL6 melanoma cells.

Science.gov (United States)

Mu, Y; Kamada, H; Kaneda, Y; Yamamoto, Y; Kodaira, H; Tsunoda, S; Tsutsumi, Y; Maeda, M; Kawasaki, K; Nomizu, M; Yamada, Y; Mayumi, T

1999-02-05

A comb-shaped polymeric modifier, SMA [poly(styrene comaleic anhydride)], which binds to plasma albumin in blood was used to modify the synthetic cell-adhesive laminin peptide YIGSR, and its inhibitory effect on experimental lung metastasis of B16-BL6 melanoma cells was examined. YIGSR was chemically conjugated with SMA via formation of an amide bond between the N-terminal amino group of YIGSR and the carboxyl anhydride of SMA. The antimetastatic effect of SMA-conjugated YIGSR was approximately 50-fold greater than that of native YIGSR. When injected intravenously, SMA-YIGSR showed a 10-fold longer plasma half-life than native YIGSR in vivo. In addition, SMA-YIGSR had the same binding affinity to plasma albumin as SMA, while native YIGSR did not bind to albumin. These findings suggested that the enhanced antimetastatic effect of SMA-YIGSR may be due to its prolonged plasma half-life by binding to plasma albumin, and that bioconjugation of in vivo unstable peptides with SMA may facilitate their therapeutic use. Copyright 1999 Academic Press.

Preparation and Characterization of Sulfonic Acid Functionalized Silica and Its Application for the Esterification of Ethanol and Maleic Acid

Science.gov (United States)

Sirsam, Rajkumar; Usmani, Ghayas

2016-04-01

The surface of commercially available silica gel, 60-200 mesh size, was modified with sulfonic acid through surface activation, grafting of 3-Mercaptopropyltrimethoxysilane, oxidation and acidification of 3-Mercaptopropylsilica. Sulfonic Acid Functionalization of Silica (SAFS) was confirmed by Fourier Transform Infra-red (FTIR) spectroscopy and thermal gravimetric analysis. Acid-base titration was used to estimate the cation exchange capacity of the SAFS. Catalytic activity of SAFS was judged for the esterification of ethanol with maleic acid. An effect of different process parameters viz. molar ratio, catalyst loading, speed of agitation and temperature were studied and optimized by Box Behnken Design (BBD) of Response Surface Methodology (RSM). Quadratic model developed by BBD-RSM reasonably satisfied an experimental and predicted values with correlation coefficient value R2 = 0.9504.

Thermal analysis and its application in evaluation of fluorinated polyimide membranes for gas separation

KAUST Repository

Qiu, Wulin; Chen, Chien-Chiang; Kincer, Matthew R.; Koros, William J.

2011-01-01

by reaction with acetic anhydride to produce polyimide (PI). The resulting polymers were characterized using thermal analysis techniques including TGA, derivative weight analysis, TGA-MS, and DSC. The decarboxylation-induced thermal cross-linking, ester cross

Study on the mechanical properties of a HMS-PP nanocomposite with a Brazilian bentonite; Estudo das propriedades mecanicas de um nanocomposito de HMS-PP com uma bentonita brasileira

Energy Technology Data Exchange (ETDEWEB)

Fermino, D M; Parra, D F; Lugao, A B; Oliani, W.L., E-mail: mfermino@usp.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Valenzuela-Diaz, F R [Universidade de Sao Paulo (USP), SP (Brazil). Escola Politecnica. Dept. de Engenharia Metalurgica e de Materiais

2010-07-01

This work concerns to the study of the mechanical behavior of the nanocomposite HMSPP - Polypropylene High Melt Strength (obtained at a dose of 12.5 kGy) and a bentonite clay Brazilian Paraiba (PB), known as 'Chocolate' in concentrations of 5 and 10% by weight, comparison of to one American Clay, cloisite 20A nanocomposite was done. Agent compatibilizer polypropylene-graft, known as maleic anhydride (PP-g-AM) was addict 3% concentration thought technique melt intercalation using a twin-screw extruder and the specimens were prepared by injection process. The mechanical behavior was evaluated by strength, flexural strength and impact tests. The morphology of the nanocomposites was studied by the technique of Scanning Electron Microscopy (SEM), while the organophilic bentonite and nanocomposites were characterized by X-ray diffraction (XRD) and infrared (FTIR). (author)