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Sample records for preparing copolymer latex

  1. PREPARATION AND PROPERTIES OF SILICONE-ACRYLATE COPOLYMER LATEX

    Institute of Scientific and Technical Information of China (English)

    Mu-jie Yang; Wei Zhang

    2004-01-01

    Silicone-acrylate copolymer latex was prepared through three different polymerization processes, i.e., the batch process, preemulsified monomer addition and the monomer addition process. The results revealed that the monomer addition process is a desirable approach to produce narrow particle size distribution latex with higher polymerization conversion and less amount of coagulum. The effect of silicone content on the glossiness and water absorption of latex film was investigated and the results showed that the glossiness of latex film is improved up to a silicone content of 10% of total monomers, but becomes impaired thereafter, whereas water absorption is reduced accordingly.

  2. Surface properties of latex film and solvent-borne film resulted from fluorinated acrylate copolymers prepared by emulsion polymerization

    Directory of Open Access Journals (Sweden)

    2007-01-01

    Full Text Available The fluorinated acrylate copolymer, poly (BMA-co-DFHMA, was prepared by emulsion polymerization using a preemulsified monomer addition process. The FTIR and 1H –NMR were used to characterize the copolymer structure. The contact angle of water on the solvent-borne film increased dramatically and reached an equilibrium value (103° when the PDFHMA content in the copolymer was only 0.97 mol%. However, the contact of water on the latex film increased slowly, and reached the equilibrium value of 99° until the fluorinated component content was as highly as 9 mol%. A similar result was observed for the oil contact angle on the two types of films. XPS results showed that when the F/C ratio on film surfaces reached equilibrium, the required content of fluorinated component in the copolymer for the solvent-borne film was much lower than that for the latex film.

  3. Preparation of Impact and Weather Resistant Copolymer

    Institute of Scientific and Technical Information of China (English)

    LIANG Tao

    2001-01-01

    @@ Synthesis method of the resin is that crosslinked polybutyl acrylate latex is used as base latex. Styrene (St) and acrylonitrile (AN) are grafted onto polybutyl acrylate latex particle and turn into core-shell copolymer. The resin is a good resin's impact modifier. There are study of influence regularity about additive emulsifier, initiator, monomer concentration, the ratio of St to AN, chain transfer to graft polymerization. A kind of core-shell resin used as impact modifier is obtained. (A) Preparation of Crosslinked Butyl Acrylate Rubber Latex

  4. PREPARATION OF HOLLOW LATEX PARTICLES BY ALKALI-ACID TREATMENT

    Institute of Scientific and Technical Information of China (English)

    郝冬梅; 王新灵; 朱卫华; 唐小真; 刘成岑; 施凯

    2001-01-01

    Hollow polymer latex particles were prepared by seeded emulsion polymerization. A seed latex consisting of styrene (St), butyl acrylate(BA) copolymer was first prepared, and seeded terpolymerization of St-BA-MA(methacrylic acid) were then carried out in the absence of surfactant. Final latex was treated by a two-step treatment under alkaline and acidic conditions, thus, the particles with hollow structure were obtained. We discussed the effects of pH value, temperature and time in alkali and acid treatment processes on hollow structure within the polymer latex particles and amount of carboxylic group on particle surface. The results show that the hollow polymer latex particles with the largest hollow size can be obtained under a certain condition (pH12.5, 90°C, 3 h in alkali treatment stage and pH2.5, 85°C, 3 h in acid treatment stage).

  5. Preparation of Impact and Weather Resistant Copolymer

    Institute of Scientific and Technical Information of China (English)

    LIANG; Tao

    2001-01-01

    Synthesis method of the resin is that crosslinked polybutyl acrylate latex is used as base latex. Styrene (St) and acrylonitrile (AN) are grafted onto polybutyl acrylate latex particle and turn into core-shell copolymer. The resin is a good resin's impact modifier. There are study of influence regularity about additive emulsifier, initiator, monomer concentration, the ratio of St to AN, chain transfer to graft polymerization. A kind of core-shell resin used as impact modifier is obtained. (A) Preparation of Crosslinked Butyl Acrylate Rubber Latex  ……

  6. Production of Natural Rubber Grafted Styrene Copolymer Latex as Water Base Coatings

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    M Utama

    2006-07-01

    Full Text Available Twelve kinds formulation of natural rubber grafted copolymer styrene (NR-g-S prepared by gamma radiation co-polymerization technique has been carried out. The characteristic of NR-g-S and its water base coating such as molecular structure, particle size, and the properties of latex and its film were evaluated. The results showed that the NR-g-S latex as a water base coating has low viscosity, height strength, good grease resistance, good flexibility, good aging and corrosion resistance on concrete cement and metal. The average particle size is between 270-300 nm, and the bonding between poly-isoprene of NRL and styrene molecules were grafted copolymer

  7. Antimicrobial films obtained from latex particles functionalized with quaternized block copolymers.

    Science.gov (United States)

    Alvarez-Paino, Marta; Juan-Rodríguez, Rafael; Cuervo-Rodríguez, Rocío; Tejero, Rubén; López, Daniel; López-Fabal, Fátima; Gómez-Garcés, José L; Muñoz-Bonilla, Alexandra; Fernández-García, Marta

    2016-04-01

    New amphiphilic block copolymers with antimicrobial properties were obtained by atom transfer radical polymerization (ATRP) and copper catalyzed cycloaddition following two approaches, a simultaneous strategy or a two-step synthesis, which were proven to be very effective methods. These copolymers were subsequently quaternized using two alkyl chains, methyl and butyl, to amplify their antimicrobial properties and to investigate the effect of alkyl length. Antimicrobial experiments in solution were performed with three types of bacteria, two gram-positive and one gram-negative, and a fungus. Those copolymers quaternized with methyl iodide showed better selectivities on gram-positive bacteria, Staphylococcus aureus and Staphylococcus epidermidis, against red blood cells, demonstrating the importance of the quaternizing agent chosen. Once the solution studies were performed, we prepared poly(butyl methacrylate) latex particles functionalized with the antimicrobial copolymers by emulsion polymerization of butyl methacrylate using such copolymers as surfactants. The characterization by various techniques served to test their effectiveness as surfactants. Finally, films were prepared from these emulsions, and their antimicrobial activity was studied against the gram-positive bacteria. The results indicate that the antimicrobial efficiency of the films depends not only on the copolymer activity but also on other factors such as the surface segregation of the antimicrobial agent to the interface.

  8. Preparation and Structural Characterization of Hydroxylethyl Methacrylate Grafted Natural Rubber Latex

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    Feiyun Wei

    2014-06-01

    Full Text Available The graft copolymer with semi-interpenetrating polymer networks (semi-IPNs from 2-hydroxyethyl methacrylate (HEMA and natural rubber (NR latex was prepared using cumene hydroperoxide and tetraethylene pentamine redox initiator system. The changes of grafting ratios and grafting efficiency with the reaction time and temperature, the concentration of crosslinking agent, initiator and monomer were investigated. The appropriate amounts of crosslinking agent (0.1phr, initiator (0.2phr and monomer (20phr and the optimum reaction conditions of 16ºC×8h were determined. The swelling temperature and times of monomers against NR latex particles were found to be significant for the grafting copolymerization and the appropriate swelling conditions were 16ºC×20h. The water contact angle measurement and platelet adhesion evaluation indicated that the hydrophilicity and blood compatibility of NR latex could be improved by grafting copolymerization with HEMA.

  9. Preparation of Inert Polystyrene Latex Particles as MicroRNA Delivery Vectors by Surfactant-Free RAFT Emulsion Polymerization.

    Science.gov (United States)

    Poon, Cheuk Ka; Tang, Owen; Chen, Xin-Ming; Pham, Binh T T; Gody, Guillaume; Pollock, Carol A; Hawkett, Brian S; Perrier, Sébastien

    2016-03-14

    We present the preparation of 11 nm polyacrylamide-stabilized polystyrene latex particles for conjugation to a microRNA model by surfactant-free RAFT emulsion polymerization. Our synthetic strategy involved the preparation of amphiphilic polyacrylamide-block-polystyrene copolymers, which were able to self-assemble into polymeric micelles and "grow" into polystyrene latex particles. The surface of these sterically stabilized particles was postmodified with a disulfide-bearing linker for the attachment of the microRNA model, which can be released from the latex particles under reducing conditions. These nanoparticles offer the advantage of ease of preparation via a scaleable process, and the versatility of their synthesis makes them adaptable to a range of applications.

  10. Properties of Polyacrylate Latex Prepared Under Different Emulsified Systems

    Institute of Scientific and Technical Information of China (English)

    CHEN Lijun; WU Fengqin

    2012-01-01

    The polyacrylate latexes were synthesized via pre-emulsified and semi-continuous seeded emulsion polymerization technology when conventional surfactant or polymerizable surfactant was used as emulsifiers.The resultant latexes and their films were characterized with the contact angle determinator and rheometer.Effect of the polymerizable surfactant on water resistance,stability and rheology of the latex was studied.Results show that the water resistance of film is increased first then decreased with the increase of the amount of the polymerizable surfactant.There exists the optimum value of the amount of the polymerizable surfactant for the water resistance of the film.In comparison with the latex prepared with the conventional surfactant,both the mechanical stability and the freezing-thaw stability of the latex are improved when the polymerizable surfactant is used during the course of the emulsion polymerization.The resultant latex has rheological properties of pseudo-plastic fluid and belongs to non-Newtonian fluid.

  11. Controllable preparation of high-yield magnetic polymer latex.

    Science.gov (United States)

    Wu, Chun-Chao; Kong, Xiang-Ming; Yang, Hai-Long

    2011-09-01

    In order to overcome the low conversion and complex post-treatment, four different polymerization procedures were adopted to prepare the magnetic polymer latexes. The results clearly show that the strategy using magnetic emulsion template-dosage is the most effective and feasible. Based on the optimized procedure, various factors including the type of initiators such as oil soluble initiator, water soluble initiator, redox initiator system, crosslinking agent, functional monomers etc. were systematically studied. Magnetic polymer latex with high monomer conversion of 83% and high magnet content of 31.8% was successfully obtained. Besides, core-shell structured magnetic polymer latex with good film forming property was also prepared, which is promising for potential applications such as magnetic coatings and modification of cementitious materials with controlled polymer location.

  12. Preparation of MMA-BA-DMAEMA Nanosized Latex

    Institute of Scientific and Technical Information of China (English)

    Yu Yang LIU; Mu Jie YANG

    2003-01-01

    The terpolymer latex of methyl methacrylate (MMA)/butyl acrylate (BA)/ dimethyl aminoethyl methacrylate (DMAEMA) with diameter of less than 100 nm was prepared by seeding semi-continuous emulsion copolymerization using APS (ammonium persulfate) / TMEDA (N,N,N, N-tetramethylethylenediamine) as the redox initiators and SDS (sodium dodecylsulfate) and OP (P-octylpolyethylene glycol phenylether) as co-emulsifiers. The factors that influenced the process stability of the copolymerization and the particle size of the latex were investigated. The addition of aqueous ammonia as coagulation inhibitor provided better process stability of the copoly- merization. The addition of acetic acid as the acidification agent caused a remarkable reduction of the latex particle size.

  13. Effect of copolymer latexes on physicomechanical properties of mortar containing high volume fly ash as a replacement material of cement.

    Science.gov (United States)

    Negim, El-Sayed; Kozhamzharova, Latipa; Gulzhakhan, Yeligbayeva; Khatib, Jamal; Bekbayeva, Lyazzat; Williams, Craig

    2014-01-01

    This paper investigates the physicomechanical properties of mortar containing high volume of fly ash (FA) as partial replacement of cement in presence of copolymer latexes. Portland cement (PC) was partially replaced with 0, 10, 20, 30 50, and 60% FA. Copolymer latexes were used based on 2-hydroxyethyl acrylate (2-HEA) and 2-hydroxymethylacrylate (2-HEMA). Testing included workability, setting time, absorption, chemically combined water content, compressive strength, and scanning electron microscopy (SEM). The addition of FA to mortar as replacement of PC affected the physicomechanical properties of mortar. As the content of FA in the concrete increased, the setting times (initial and final) were elongated. The results obtained at 28 days of curing indicate that the maximum properties of mortar occur at around 30% FA. Beyond 30% FA the properties of mortar reduce and at 60% FA the properties of mortar are lower than those of the reference mortar without FA. However, the addition of polymer latexes into mortar containing FA improved most of the physicomechanical properties of mortar at all curing times. Compressive strength, combined water, and workability of mortar containing FA premixed with latexes are higher than those of mortar containing FA without latexes.

  14. Effect of Copolymer Latexes on Physicomechanical Properties of Mortar Containing High Volume Fly Ash as a Replacement Material of Cement

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    El-Sayed Negim

    2014-01-01

    Full Text Available This paper investigates the physicomechanical properties of mortar containing high volume of fly ash (FA as partial replacement of cement in presence of copolymer latexes. Portland cement (PC was partially replaced with 0, 10, 20, 30 50, and 60% FA. Copolymer latexes were used based on 2-hydroxyethyl acrylate (2-HEA and 2-hydroxymethylacrylate (2-HEMA. Testing included workability, setting time, absorption, chemically combined water content, compressive strength, and scanning electron microscopy (SEM. The addition of FA to mortar as replacement of PC affected the physicomechanical properties of mortar. As the content of FA in the concrete increased, the setting times (initial and final were elongated. The results obtained at 28 days of curing indicate that the maximum properties of mortar occur at around 30% FA. Beyond 30% FA the properties of mortar reduce and at 60% FA the properties of mortar are lower than those of the reference mortar without FA. However, the addition of polymer latexes into mortar containing FA improved most of the physicomechanical properties of mortar at all curing times. Compressive strength, combined water, and workability of mortar containing FA premixed with latexes are higher than those of mortar containing FA without latexes.

  15. Polymer composites prepared from heat-treated starch and styrene-butadiene latex

    Science.gov (United States)

    Thermoplastic starch/latex polymer composites were prepared using styrene–butadiene (SB) latex and heat-treated cornstarch. The composites were prepared in a compression mold at 130 °C, with starch content 20%. An amylose-free cornstarch, waxy maize, was used for this research and the heat treatment...

  16. Isotactic polypropylene/carbon nanotube composites prepared by latex technology: electrical conductivity study

    NARCIS (Netherlands)

    Grossiord, N.; Wouters, M.E.L.; Miltner, H.E.; Lu, K.; Loos, J.; Mele, B.V.; Koning, C.E.

    2010-01-01

    Several series of nanocomposites were prepared using a latex-based process, the main step of which consisted of mixing an aqueous suspension of exfoliated carbon nanotubes (CNTs) and a polymer latex. In the present work, a systematic study on the electrical properties of fully amorphous (polystyrene

  17. PREPARATION AND STABILITY OF POLYSTYRENE LATEXES USING POLYSOAPS AS EMULSIFIERS

    NARCIS (Netherlands)

    YANG, YJ; ENGBERTS, JBFN

    Microemulsions of styrene can be polymerized at 70-degrees in the presence of polysoaps as emulsifiers to produce stable polystyrene latexes. The effects of polymerization conditions on the molecular weights, molecular weight distribution, particle size and particle size distribution of the latexes

  18. [Preparation of magnetic latexes and their use for the immunodetection of microbial antigens].

    Science.gov (United States)

    Kal'noĭ, S M; Zharnikova, I V; Zaĭtsev, A A; Bondarenko, A I; Borzdova, I Iu; Ostapovich, V V; Kurilova, A A

    2010-01-01

    The possibility of detecting antigens of plague, tularemia, and brucellosis microbes with magnetic latex (ML)-based test systems has been demonstrated. MLs were prepared from latexes (polyacroleine microspheres, 1.2-1.8 +/- 0.1 microm) by exposing the particles to a 25-35%-solution of ferrous sulfate for 0.5 h and then to a 15-25%-aqueous solution of ammonia for 0.5 h in a 100 degrees C water bath and dehydrating after each operation. The possibility of preparing magnetic latex immunosorbents (MLIS) by ligand immobilization on ML and using them in magnetic latex ELISA (ML-ELISA) for the detection of microbial antigens was demonstrated. The detection limit in ML-ELISA equaled 10(2)-10(3) microbial cells in 1 ml (cells/ml). Relative experimental error was not higher than 8%.

  19. Preparation of Styrene-acrylate Latex Used in Ultra-low VOC Building Internal Wall Coating

    Institute of Scientific and Technical Information of China (English)

    CHEN Lijun; WU Fengqin; ZHUANG Xinyu; YANG Jian; LI Rongxian

    2008-01-01

    Styrene-acrylate latex with high glass transition temperature(Tg),low minimum film forming temperature(MFT)and good stability was prepared via core-shell emulsion polymerization.With semicontinuous process,high conversion rate of monomer and low gel rate were achieved.The weight ratio of core monomer to shell monomer was approximately 1.35.It is found that many factors such as emulsifiers,initiators,reaction temperature,pH value and polymerization technology have influences on the permormance of styrene-acrylate latex.The prepared latex was characterized by TEM and FTIR.The obtained latex with T of20.57℃,MFT of 5.0℃,and good stability,had good stability of film forming.

  20. PREPARATION AND SURFACE PROPERTIES OF ACRYLIC COPOLYMERS CONTAINING FLUORINATED MONOMERS

    Institute of Scientific and Technical Information of China (English)

    Tai-jiang Gui; Hao Wei; Ying Zhao; Xiu-lin Wang; Du-jin Wang; Duan-fu Xu

    2006-01-01

    A series of copolymers comprising butylmethacrylate, styrene, butylacrylate, hydroxypropyl acrylate and perfluoroalkyl methacrylate were synthesized by the free radical polymerization using BPO as an initiator. The surface property of the copolymer films was subsequently characterized. The contact angle measurements and energy dispersive analysis of X-ray (EDAX) show that the length and content ofperfluoroalkyl side chains in the copolymers are crucial for the preparation of the film with low surface energy. At a given content of fluorinated monomers in the copolymers, the longer the perfluoroalkyl side chain, the larger the water contact angle of the copolymer films will be. On the other hand, the higher the content of fluorinated monomers, the lower the surface energy is. The water contact angle increases with the increase of the fluorinated monomer content and reaches a plateau at 3 wt% of fluorinated monomer content.

  1. Preparation and icephobic properties of polymethyltrifluoropropylsiloxane-polyacrylate block copolymers

    Science.gov (United States)

    Li, Xiaohui; Zhao, Yunhui; Li, Hui; Yuan, Xiaoyan

    2014-10-01

    Five polymethyltrifluoropropylsiloxane (PMTFPS)-polyacrylate block copolymers (PMTFPS-b-polyacrylate) were synthesized by free radical polymerization of methyl methacrylate, n-butyl acrylate and hydroxyethyl methacrylate using PMTFPS macroazoinitiator (PMTFPS-MAI) in range of 10-50 mass percentages. The morphology, surface chemical composition and wettability of the prepared copolymer films were investigated by transmission electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, and water contact angle measurement. Delayed icing time and ice shear strength of the films were also detected for the icephobic purpose. The surface morphologies of the copolymers were different from those of the bulk because of the migration of the PMTFPS segments to the air interface during the film formation. Maximal delayed icing time (186 s at -15 °C) and reduction of the ice shear strength (301 ± 10 kPa) which was significantly lower than that of polyacrylates (804 ± 37 kPa) were achieved when the content of PMTFPS-MAI was 20 wt%. The icephobicity of the copolymers was attributed primarily to the enrichment of PMTFPS on the film surface and synergistic effect of both silicone and fluorine. Thus, the results show that the PMTFPS-b-polyacrylate copolymer can be used as icephobic coating materials potentially.

  2. Preparation and characterization of inorganic-organic trilayer core-shell polysilsesquioxane/polyacrylate/polydimethylsiloxane hybrid latex particles

    Science.gov (United States)

    Bai, Ruiqin; Qiu, Teng; Han, Feng; He, Lifan; Li, Xiaoyu

    2012-07-01

    The inorganic-organic trilayer core-shell polysilsesquioxane/polyacrylate/polydimethylsiloxane hybrid latex particles have been successfully prepared via seeded emulsion polymerization of acrylate monomers and octamethylcyclotetrasiloxane (D4) gradually, using functional polymethacryloxypropylsilsesquioxane (PSQ) latex particles with reactive methacryloxypropyl groups synthesized by the hydrolysis and polycondensation of (3-methacryloxypropyl)trimethoxysilane in the presence of mixed emulsifiers as seeds. The FTIR spectra show that acrylate monomers and D4 are effectively involved in the emulsion copolymerization and formed the polydimethylsiloxane-containing hybrid latex particles. Transmission electron microscopy (TEM) and dynamic light scattering (DLS) confirm that the resultant hybrid latex particles have evident trilayer core-shell structure and a narrow size distribution. XPS analysis also indicates that polysilsesquioxane/polyacrylate/polydimethylsiloxane hybrid latex particles have been successfully prepared and PDMS is rich in the surface of the hybrid latex film. Additionally, compared with the hybrid latex film without PDMS, the hybrid latex film containing PDMS shows higher hydrophobicity (water contact angle) and lower water absorption.

  3. Preparation and characterization of inorganic-organic trilayer core-shell polysilsesquioxane/polyacrylate/polydimethylsiloxane hybrid latex particles

    Energy Technology Data Exchange (ETDEWEB)

    Bai Ruiqin [College of Materials Science and Engineering, State Key Laboratory of Organic-Inorganic Composite, Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Qiu Teng, E-mail: qiuteng@mail.buct.edu.cn [College of Materials Science and Engineering, State Key Laboratory of Organic-Inorganic Composite, Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Han Feng; He Lifan [College of Materials Science and Engineering, State Key Laboratory of Organic-Inorganic Composite, Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Li Xiaoyu, E-mail: lixy@mail.buct.edu.cn [College of Materials Science and Engineering, State Key Laboratory of Organic-Inorganic Composite, Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China)

    2012-07-15

    The inorganic-organic trilayer core-shell polysilsesquioxane/polyacrylate/polydimethylsiloxane hybrid latex particles have been successfully prepared via seeded emulsion polymerization of acrylate monomers and octamethylcyclotetrasiloxane (D{sub 4}) gradually, using functional polymethacryloxypropylsilsesquioxane (PSQ) latex particles with reactive methacryloxypropyl groups synthesized by the hydrolysis and polycondensation of (3-methacryloxypropyl)trimethoxysilane in the presence of mixed emulsifiers as seeds. The FTIR spectra show that acrylate monomers and D{sub 4} are effectively involved in the emulsion copolymerization and formed the polydimethylsiloxane-containing hybrid latex particles. Transmission electron microscopy (TEM) and dynamic light scattering (DLS) confirm that the resultant hybrid latex particles have evident trilayer core-shell structure and a narrow size distribution. XPS analysis also indicates that polysilsesquioxane/polyacrylate/polydimethylsiloxane hybrid latex particles have been successfully prepared and PDMS is rich in the surface of the hybrid latex film. Additionally, compared with the hybrid latex film without PDMS, the hybrid latex film containing PDMS shows higher hydrophobicity (water contact angle) and lower water absorption.

  4. Preparation of sulphonate-containing core/shell latex particles via seeded emulsion copolymerization

    Institute of Scientific and Technical Information of China (English)

    Ji Shuai Wang; Wei Deng; Yun Shen Chen; Cheng You Kan

    2010-01-01

    In this study,P(St-MAA)seed latex particles were first prepared via soap-free emulsion polymerization of styrene(St)and methacrylic acid(MAA),then the seed particles were allowed to swell with St at room temperature,and the P(St-MAA)/P(St-NaSS)core/shell latex particles were then synthesized via seeded emulsion copolymerization of St and sodium styrene sulphonate(NaSS)using AIBN as initiator in the presence of N,N'-methylenebisacrylamide(BAA,water-soluble crosslinker).Results showed that the polymerization could be carried out smoothly when the ratio of BAA to total monomers was less than 3 mol%,the narrow dispersed P(St-MAA)seed particles with the diameter of 150 nm and the P(St-MAA)/P(St-NaSS)core/shell latexes with the particle size of about 200 nm were synthesized.When the 25/75 mole ratio of NaSS/(St+MAA)and 2 mol% of BAA were used in the seeded emulsion polymerization,the resulted P(St-MAA)/P(St-NaSS)latex product showed a low weight loss after water extraction,and the NaSS unit content in the whole particle and in the shell reached 11.7 mol% and 34.6 mol%,respectively.

  5. Preparation and icephobic properties of polymethyltrifluoropropylsiloxane–polyacrylate block copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xiaohui; Zhao, Yunhui [School of Materials Science and Engineering, and Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin 300072 (China); Li, Hui [School of Chemistry and Chemical Engineering, Shandong Key Laboratory of Fluorine Chemistry and Chemical Engineering Materials, University of Jinan, Jinan 250022 (China); Yuan, Xiaoyan, E-mail: xyuan28@yahoo.com [School of Materials Science and Engineering, and Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin 300072 (China)

    2014-10-15

    Highlights: • PMTFPS–b-polyacrylate copolymers in five different compositions were synthesized. • Enrichment of PMTFPS amounts at the surface made high F/Si value. • Icing delay time was related to the surface roughness. • Ice shear strength was decreased by the synergistic effect of silicone and fluorine. - Abstract: Five polymethyltrifluoropropylsiloxane (PMTFPS)–polyacrylate block copolymers (PMTFPS–b-polyacrylate) were synthesized by free radical polymerization of methyl methacrylate, n-butyl acrylate and hydroxyethyl methacrylate using PMTFPS macroazoinitiator (PMTFPS-MAI) in range of 10–50 mass percentages. The morphology, surface chemical composition and wettability of the prepared copolymer films were investigated by transmission electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, and water contact angle measurement. Delayed icing time and ice shear strength of the films were also detected for the icephobic purpose. The surface morphologies of the copolymers were different from those of the bulk because of the migration of the PMTFPS segments to the air interface during the film formation. Maximal delayed icing time (186 s at −15 °C) and reduction of the ice shear strength (301 ± 10 kPa) which was significantly lower than that of polyacrylates (804 ± 37 kPa) were achieved when the content of PMTFPS-MAI was 20 wt%. The icephobicity of the copolymers was attributed primarily to the enrichment of PMTFPS on the film surface and synergistic effect of both silicone and fluorine. Thus, the results show that the PMTFPS–b-polyacrylate copolymer can be used as icephobic coating materials potentially.

  6. Plasma etching of polystyrene latex particles for the preparation of graphene oxide nanowalls

    Directory of Open Access Journals (Sweden)

    Bon Bittolo Silvia

    2012-01-01

    Full Text Available Graphene oxide nanowalls were prepared by casting a water dispersion of polystyrene latex particles onto a graphene oxide film followed by tetrafluoromethane plasma etching. Mild plasma etching conditions allow one to retain the oxygen functional groups on the graphene oxide nanowalls. It was found that the exposure to a xenon light source of such graphene oxide nanowalls coated with a gold thin film results in an increase of the electrical conductivity.

  7. Preparation and characterization of latex particles as potential physical shale stabilizer in water-based drilling fluids.

    Science.gov (United States)

    Liu, Junyi; Qiu, Zhengsong; Huang, Wei'an; Song, Dingding; Bao, Dan

    2014-01-01

    The poly(styrene-methyl methacrylate) latex particles as potential physical shale stabilizer were successfully synthesized with potassium persulfate as an initiator in isopropanol-water medium. The synthesized latex particles were characterized by Fourier transform infrared spectroscopy (FT-IR), particle size distribution measurement (PSD), transmission electron microscopy (TEM), and thermal gravimetric analysis (TGA). FT-IR and TGA analysis confirmed that the latex particles were prepared by polymerization of styrene and methyl methacrylate and maintained good thermal stability. TEM and PSD analysis indicated that the spherical latex particles possessed unimodal distribution from 80 nm to 345 nm with the D90 value of 276 nm. The factors influencing particle size distribution (PSD) of latex particles were also discussed in detail. The interaction between latex particles and natural shale cores was investigated quantitatively via pore pressure transmission tests. The results indicated that the latex particles as potential physical shale stabilizer could be deformable to bridge and seal the nanopores and microfractures of shale to reduce the shale permeability and prevent pore pressure transmission. What is more, the latex particles as potential physical shale stabilizer work synergistically with chemical shale stabilizer to impart superior shale stability.

  8. Preparation and Characterization of Latex Particles as Potential Physical Shale Stabilizer in Water-Based Drilling Fluids

    Directory of Open Access Journals (Sweden)

    Junyi Liu

    2014-01-01

    Full Text Available The poly(styrene-methyl methacrylate latex particles as potential physical shale stabilizer were successfully synthesized with potassium persulfate as an initiator in isopropanol-water medium. The synthesized latex particles were characterized by Fourier transform infrared spectroscopy (FT-IR, particle size distribution measurement (PSD, transmission electron microscopy (TEM, and thermal gravimetric analysis (TGA. FT-IR and TGA analysis confirmed that the latex particles were prepared by polymerization of styrene and methyl methacrylate and maintained good thermal stability. TEM and PSD analysis indicated that the spherical latex particles possessed unimodal distribution from 80 nm to 345 nm with the D90 value of 276 nm. The factors influencing particle size distribution (PSD of latex particles were also discussed in detail. The interaction between latex particles and natural shale cores was investigated quantitatively via pore pressure transmission tests. The results indicated that the latex particles as potential physical shale stabilizer could be deformable to bridge and seal the nanopores and microfractures of shale to reduce the shale permeability and prevent pore pressure transmission. What is more, the latex particles as potential physical shale stabilizer work synergistically with chemical shale stabilizer to impart superior shale stability.

  9. Preparation of diarylethene copolymers and their photoinduced refractive index change

    Science.gov (United States)

    Cho, S. Y.; Yoo, M.; Shin, H.-W.; Ahn, K.-H.; Kim, Y.-R.; Kim, E.

    2003-01-01

    Diarylethene copolymers were synthesized from 1-(6 '-vinyl-2 '-methylbenzo[ b]thiophene-3 '-yl)-2-(2 ''-methylbenzo [ b]thiophene-3 ''-yl)hexafluorocyclopentene (VMBTF6) and 1-[6 '-(4 '''-vinylbenzoyl)-2 '-methylbenzo[ b]thiophene-3 '-yl]-2-(2 ''-methylbenzo[ b]thiophene-3 ''-yl)hexafluorocyclopentene (VBMBTF6) via living free radical techniques using stable TEMPO derivatives. The diarylethene content was controlled by the feed ratio of diarylethene derivatives and styrene. Transparent photochromic polymer films were prepared from the diarylethene copolymers with narrow molecular weight dispersion (PD˜1.3) by spin coating method. Photoinduced refractive index changes (Δ nTE) of the polymer films, with 25 mol% of diaryethene content, accompanied by the photochromic change were determined as 0.0009 and 0.0030 for poly(styrene- ran -VMBTF6) and poly(styrene- ran-VBMBTF6), respectively.

  10. Properties of natural rubber/attapulgite composites prepared by latex compounding method: Effect of filler loading

    Energy Technology Data Exchange (ETDEWEB)

    Muttalib, Siti Nadzirah Abdul, E-mail: sitinadzirah.amn@gmail.com; Othman, Nadras, E-mail: srnadras@usm.my; Ismail, Hanafi, E-mail: ihanafi@usm.my [School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, Seri Ampangan, 14300 Nibong Tebal, Pulau Pinang (Malaysia)

    2015-07-22

    This paper reports on the effect of filler loading on properties of natural rubber (NR)/attapulgite (ATP) composites. The NR/ATP composites were prepared by latex compounding method. It is called as masterbatch. The masterbatch was subsequently added to the NR through melt mixing process. The vulcanized NR/ATP composites were subjected to mechanical, swelling and morphological tests. All the results were compared with NR/ATP composites prepared by conventional system. The composites from masterbatch method showed better results compared to composites prepared by conventional method. They have higher tensile properties, elongation at break and tear strength. The images captured through scanning electron microscopy test revealed the improvement of tensile strength in masterbatch NR/ATP composites. It can be seen clearly that masterbatch NR/ATP have better filler dispersion compared to conventional method NR/ATP composites.

  11. Preparation of magnetic rubber with high mechanical properties by latex compounding method

    Science.gov (United States)

    Hou, Chunlin; Gao, Li; Yu, Hailing; Sun, Youyi; Yao, Junru; Zhao, Guizhe; Liu, Yaqing

    2016-06-01

    the magnetic rubber based on Fe3O4 nanoparticles and nature rubber were prepared by latex compounding method, in which stable Fe3O4 aqueous solutions were mixed with natural rubber latex and additives. This process was fast, versatile, reliable, safe, environmentally friendly and inexpensive. What's more, it was found that the magnetic and mechanical properties of magnetic rubber increased together with increase in doping content of Fe3O4 nanoparticles. Especially, it was demonstrated that the tensile strength (25.0 Mpa) of magnetic rubber was improved to be 478.0% comparing to neat natural rubber (5.2 Mpa), which was 5 times higher than maximal value reported in previous work. At the same time, the magnetic rubber revealed better thermal stability and solvent resistance comparing to the neat natural rubber, too. The work dose not only provides a new way to environmentally friendly preparation of magnetic rubber at low temperature, but also improve the mechanical and magnetic properties of magnetic rubber applied in industry.

  12. Natural rubber latex blended polystyrene emulsion for dipping products: preparation and properties

    Directory of Open Access Journals (Sweden)

    Kovuttikulrangsie, S.

    2004-05-01

    Full Text Available Deproteinized natural rubber latex (DPNR was prepared using KAO protease enzyme to digest proteins from natural rubber low ammonia concentrated latex (NR-LA. Polystyrene latex (PS was synthesized by emulsion polymerization technique for blending with natural rubber. The maximum fraction of PS blended NR-LA or DPNR used to obtain a homogenous film was 20% w/w. The 300% modulus of PS blended NR film was increased before and after aging at 100ºC for 22 hrs. The tensile strength and elongation at break were increased at NR/PS = 95/5 w/w and tended to decrease as PS blended fraction increased. DPNR films had a lower friction coefficient than NR-LA films. PS blended NR-LA or DPNR would decrease the friction coefficient of films. The rubber-surfaced friction is reduced. The extractable protein of NR-LA film was higher than 200 μg/g whereas that of DPNR film was lower than 50 μg/g. PS blended NR-LA and DPNR could reduce the extractable protein to less than 60 μg/g and 30μg/g, respectively. The physical properties of PS blended NR-LA met ASTM D3577 and ASTM D3578 standards for dipping products of surgical gloves and examination gloves at the maximum fraction of PS 15% w/w and 20% w/w, respectively, whereas PS blended DPNR only met ASTM D3577 standard at the maximum fraction of PS < 5% w/w.

  13. Preparation of Mosaic Latex Particles%镶嵌型乳胶粒子的合成

    Institute of Scientific and Technical Information of China (English)

    李效玉; 石淑先; 寇奕; 董汉鹏; 夏宇正

    2001-01-01

    A new kind of mosaic latex particles with gradient distribution of hard polymer have been synthesized through two-stage emulsion polymerization based on natural rubber latex.One or two or three of styrene,methyl methacrylate,acrylonitrile,isobornyl acrylate were used as hard monomer in order to prepare interpenetrating polymer network.When oleinic acid was selected as emulsifier,tbutylhydroperoxide-tetraethylene pentamine as oxi-reduction initiation system,the polymerization proceeded for 6 h in natural rubber latex smoothly with the 99% conversion of monomer.The effects of emulsifiers and the initiators on the polymerization were studied; the effects of crosslinker,swelling degree,hard monomer on morphology of the title latex particles were also investigated.The result of morphology analysis of the latex showed that the latex particle was mosaic structure with hard polymer gradient distributed.%以苯乙烯、甲基丙烯酸甲酯、丙烯腈等单体或它们的混合物为硬单体,天然胶乳为弹性组分,经多步种子乳液聚合法制得了在天然胶乳的粒子上镶嵌硬聚合物相的互穿网络型乳胶粒子.考察了十二烷基硫酸钠、十二烷基苯磺酸钠、壬基酚聚氧乙烯醚、油酸等乳化体系,过硫酸钾、过氧化苯甲酰热引发体系及异丙苯过氧化氢-四乙烯五胺、叔丁基过氧化氢-四乙烯五胺等氧化还原引发体系对聚合反应的影响.研究了交联剂用量对互穿结合率、溶胶含量的影响及溶胀时间、硬单体组成、乳化剂种类对乳胶粒子形态的影响,确定了适宜的聚合配方和工艺条件.透射电镜观察乳粒形态结果表明,单一使用极性或非极性单体,仅得到核-壳结构乳液,而采用不同极性单体复合、溶胀、互穿,得到的是镶嵌硬聚合物型乳粒结构.

  14. PREPARATION AND PROPERTIES OF ABSORBABLE FIBERS FROM L-LACTIDE COPOLYMERS

    NARCIS (Netherlands)

    PENNING, JP; PENNINGS, AJ

    1993-01-01

    Absorbable fibres have been prepared from various copolymers Of L-lactide with either D-lactide or epsilon-caprolactone. The lower crystallinity of these copolymers, compared with the homopolymer, is desirable in the light of their potential use as an absorbable suture material and has a pronounced

  15. Preparation of Pickering double emulsions using block copolymer worms.

    Science.gov (United States)

    Thompson, Kate L; Mable, Charlotte J; Lane, Jacob A; Derry, Mathew J; Fielding, Lee A; Armes, Steven P

    2015-04-14

    The rational formulation of Pickering double emulsions is described using a judicious combination of hydrophilic and hydrophobic block copolymer worms as highly anisotropic emulsifiers. More specifically, RAFT dispersion polymerization was utilized to prepare poly(lauryl methacrylate)-poly(benzyl methacrylate) worms at 20% w/w solids in n-dodecane and poly(glycerol monomethacrylate)-poly(2-hydroxypropyl methacrylate)-poly(benzyl methacrylate) worms at 13% w/w solids in water by polymerization-induced self-assembly (PISA). Water-in-oil-in-water (w/o/w) double emulsions can be readily prepared with mean droplet diameters ranging from 30 to 80 μm using a two-stage approach. First, a w/o precursor emulsion comprising 25 μm aqueous droplets is prepared using the hydrophobic worms, followed by encapsulation within oil droplets stabilized by the hydrophilic worms. The double emulsion droplet diameter and number of encapsulated water droplets can be readily varied by adjusting the stirring rate employed during the second stage. For each stage, the droplet volume fraction is relatively high at 0.50. The double emulsion nature of the final formulation was confirmed by optical and fluorescence microscopy studies. Such double emulsions are highly stable to coalescence, with little or no change in droplet diameter being detected over storage at 20 °C for 10 weeks as judged by laser diffraction. Preliminary experiments indicate that the complementary o/w/o emulsions can also be prepared using the same pair of worms by changing the order of homogenization, although somewhat lower droplet volume fractions were required in this case. Finally, we demonstrate that triple and even quadruple emulsions can be formulated using these new highly anisotropic Pickering emulsifiers.

  16. Effect of Polyvinylpyrrolidone on the Morphologies of Latex Films and Air Permeability of the Latex Finished Fabrics

    Institute of Scientific and Technical Information of China (English)

    SHEN Yi-feng; YE Jia-jia; YANG Lei; WU Ming-hua; NI Tian-xiang

    2010-01-01

    Low air permeability is a common problem happening to the coating finished and pigment dyed fabrics.To tackle the problem,styrene and butyl acrylate copolymer latex was prepared and used as substitute for the binder.Then,polyvinylpyrrolidoue(PVP)was fed into the latex.It was expected that pores could form in the resulting latex film after being rinsed.The morphologies of the latex films were analysized by scanning electric microscope(SEM).It was found that the continuity of the latex films decreased greatly because of the addition of PVP,leading to the loss of the stress at break of the films.After rinsing with methanol aqueous solution,PVP was easily leached off and(macro)void was formed in the latex films.The size of the void decreased with the increase of the PVP concentration.Then,the latex with and without PVP was used to finish the cotton fabrics and engaged as binder in pigment dyeing.After PVP was rinsed out,the air permeability of the fabrics improved greatly,which recovered to that of the unfinished one.In the meantime,the color fastness to rubbing was little affected.So,the method of PVP addition could be termed as an efficient way to improve the air permeability in coating and dyeing industry.

  17. PREPARATION AND APPLICATION OF PHOTOSENSITIVE COPOLYMERS FOR PDP BARRIER RIBS FORMED BY PHOTOLITHOGRAPHY

    Institute of Scientific and Technical Information of China (English)

    Tao Zhang; Qian-wen Dong; Wei Zhang; Jie Wei

    2013-01-01

    In this work,the photosensitive paste was prepared.It was comprised of inorganic particles and a photosensitive organic component.The inorganic particles included glass,ceramics,and metals.The organic component should contain at least the following photosensitive materials:photosensitive monomers,photoreactive copolymer and photopolymerization initiators.The photoreactive copolymer played a role of an adhesive in the photosensitive paste.Meanwhile in the development stage,the carboxyl groups of the copolymer reacted with the alkalescent developer.Following this,the unexposed part must be removed and an excellent pattern can be formed.A series of three-component acrylic copolymers (MAA/St/MMA) were designed,and then synthesized via free radical polymerization.Subsequently glycidyl methacrylate (GMA) was employed to modify the prepared copolymers through ring-opening reactions between the carboxyl groups and the epoxide groups.Eventually the photosensitive copolymers were obtained and used to form the barrier ribs of PDPs.The chemical structure,glass transition temperature,acid value and molecular weight of photosensitive copolymers had different effects on the structure and pattern of PDP barrier ribs.Through analyzing effects of different polymer performance parameters on the patterns of barrier ribs,the optimal photosensitive copolymer was acquired.

  18. Preparation, Stability, and Bio-Compatability of Block Copolymer Vesicles

    Science.gov (United States)

    Discher, Dennis; Lee, James C.-M.; Bermudez, Harry; Bates, Frank; Discher, Bohdana

    2001-03-01

    Vesicles made completely from diblock copolymers polymersomes can be stably prepared by a wide range of techniques common to liposomes. Processes such as film rehydration, sonication, and extrusion can generate many micron giants as well as monodisperse, 100 nm vesicles of PEO-PEE (polyethyleneoxide polyethylethylene) or PEO PBD (polyethyleneoxide polybutadiene). These thick-walled vesicles of polymer can encapsulate macromolecules just as liposomes can, but, unlike many pure liposome systems, these polymersomes exhibit no in-surface thermal transitions and a sub-population even survive autoclaving. Suspension in blood plasma has no immediate ill-effect on vesicle stability, and neither adhesion nor stimulation of phagocytes are apparent when giant polymersomes are held in direct, protracted contact. Proliferating cells, in addition, are unaffected when cultured for an extended time with an excess of polymersomes, and several injections of 10 mg doses into rats show no ill-effect. The results are consistent with the steric stabilization that PEG-lipid can impart to liposomes, but the present single-component polymersomes are far more stable mechanically and are not limited by PEG driven micellization.

  19. Synthesis of Fluorinated Acrylate Ternary Copolymer Latex by Miniemulsion Polymerization and Characterization%细乳液聚合制备含氟丙烯酸酯三元共聚物及性能表征

    Institute of Scientific and Technical Information of China (English)

    高秀云; 任小翠; 邹祥龙; 兰云军

    2013-01-01

    Using SDS and AEO-9 as the emulsifiers, stable fluoroacrylate ternary copolymer emulsion were made by miniemulsion polymerization with fluoroacrylate (FA), butyl acrylate (BA), methyl methacrylate (MMA) as the monomers. The composition of copolymer were demonstrated by FT-IR and 'H NMR. The influences of ultrasonic power, ultrasonic time, FA content and emulsifier dosage on emulsion particle size and its distribution index were investigated and the surface property of films was studied by Wilhelmy method. Ultrasonic power was 300W, ultrasonic time was 3min, emulsifier dosage was 2.5wt% and the fluorine content was more than 4wt% which were the better miniemulsion polymerization process in this work; Some properties of fluoroacrylate copolymer latex of miniemulsion were improved, The prepared polymer emulsion membrane had excellent hydrophobic and oleophobic property with low fluorine content.%本工作以十二烷基硫酸钠(SDS)和脂肪醇聚氧乙烯醚(AEO-9)为乳化剂,采用细乳液聚合的方法,制备了甲基丙烯酸甲酯(MMA)、丙烯酸丁酯(BA)和全氟烷基丙烯酸酯(FA)三元共聚物.采用FT-IR、1H-NMR对聚合物的结构进行了表征;采用接触角法研究聚合物乳胶膜的表面性能.系统考察了超声均质强度(超声功率)、超声时间、FA用量、乳化剂用量等因素对细乳液聚合稳定性和乳液粒径及其分布的影响,优化的较佳细乳化工艺为:超声功率300 W、超声时间3 min、乳化剂用量为2.5%,FA单体质量分数>4%;所制备的聚合物乳胶膜在低含氟量下即表现出优异的疏水疏油性能.

  20. Preparation and characterization of lignin based macromonomer and its copolymers with butyl methacrylate.

    Science.gov (United States)

    Liu, Xiaohuan; Wang, Jifu; Yu, Juan; Zhang, Mingming; Wang, Chunpeng; Xu, Yuzhi; Chu, Fuxiang

    2013-09-01

    Copolymerization of butyl methacrylate (BMA) with biobutanol lignin (BBL) was achieved by free-radical polymerization (FRP) using a lignin-based macromonomer. The lignin-based macromonomer containing acrylic groups was prepared by reacting acryloyl chloride with biobutanol lignin using triethylamine (TEA) as absorb acid agentin. From the results of elemental analysis and GPC, the average degree of polymerization (DP) of BBL was estimated to be five. A detailed molecular characterization has been performed, including techniques such as (1)H NMR, (13)C NMR and UV-vis spectroscopies, which provided quantitative information about the composition of the copolymers. The changes in the solubility of lignin-g-poly(BMA) copolymers in ethyl ether were dependent on the length of poly(BMA) side chain. TGA analysis indicated that the lignin-containing poly(BMA) graft copolymers exhibited high thermal stability. The bulky aromatic group of lignin increased the glass-transition temperature of poly(BMA). In order to confirm the main structure of copolymer, (AC-g-BBL)-co-BMA copolymer was also synthesized by atom transfer radical polymerization (ATRP), and the results revealed that the copolymer prepared by ATRP had the same solution behavior as that prepared by FRP, and the lignin-based macromonomer showed no homopolymerizability due to the steric hindrance. In addition, the lignin-co-BMA copolymer had a surprisingly higher molecular weight than poly(BMA) under the same reaction condition, suggesting that a branched lignin based polymer could be formed.

  1. Preparation and modification of itaconic anhydride–methyl methacrylate copolymers

    Directory of Open Access Journals (Sweden)

    MILOS B. MILOVANOVIC

    2007-12-01

    Full Text Available The free radical copolymerisation of itaconic anhydride and methyl methacrylate in solution was studied at 60 °C. The copolymer composition was determined by 1H-NMR spectroscopy and the obtained monomer reactivity ratios were calculated, rITA = 1.35±0.11; rMMA = 0.22±0.22 (by the Fineman–Ross method and rITA = 1.27±0.38; rMMA = 0.10±0.05 (by the Mayo–Lewis method. The synthesised copolymers were modified by reaction with di-n-butyl amine. The copolymer composition after amidation was determined by elemental analysis via the nitrogen content. Amidation of the anhydride units in the copolymers with di-n-butyl amine resulted in complete conversion to itaconamic acid.

  2. Studies on Preparation of Poly(3,4-Dihydroxyphenylalanine-Polylactide Copolymers and the Effect of the Structure of the Copolymers on Their Properties

    Directory of Open Access Journals (Sweden)

    Dongjian Shi

    2016-03-01

    Full Text Available Properties of copolymers are generally influenced by the structure of the monomers and polymers. For the purpose of understanding the effect of polymer structure on the properties, two kinds of copolymers, poly(3,4-dihydroxyphenylalanine-g-polylactide and poly(3,4-dihydroxyphenylalanine-b-polylactide (PDOPA-g-PLA and PDOPA-b-PLA were designed and prepared by ring-opening polymerization of lactide with pre-prepared PDOPA as the initiator and the amidation of the functional PLA and PDOPA oligomer, respectively. The molecular weight and composition of the copolymers could be adjusted by changing the molar ratio of LA and DOPA and were confirmed by gel permeation chromatography (GPC and proton nuclear magnetic resonance (1H NMR spectra. The obtained copolymers with graft and block structures showed high solubility even in common organic solvents. The effects of the graft and block structures on the thermal and degradation properties were also detected. The PDOPA-g-PLA copolymers showed higher thermal stability than the PDOPA-b-PLA copolymers, due to the PDOPA-g-PLA copolymers with regular structure and strong π-π stacking interactions among the intermolecular and intramolecular chains. In addition, the degradation results showed that the PDOPA-g-PLA copolymers and the copolymers with higher DOPA composition had quicker degradation speeds. Interestingly, both two kinds of copolymers, after degradation, became undissolved in the organic solvents because of the oxidation and crosslinking formation of the catechol groups in the DOPA units during degradation in alkaline solution. Moreover, fluorescent microscopy results showed good biocompatibility of the PDOPA-g-PLA and PDOPA-b-PLA copolymers. The PDOPA and PLA copolymers have the potential applications to the biomedical and industrial fields.

  3. Preparation of polysilsesquioxane-urethaneacrylate copolymer film reinforced with chitin nanofibers.

    Science.gov (United States)

    Ifuku, Shinsuke; Ikuta, Akiko; Hosomi, Tetsuya; Kanaya, Shingo; Shervani, Zameer; Morimoto, Minoru; Saimoto, Hiroyuki

    2012-07-01

    Chitin nanofibers (CNFs) reinforced silsesquioxane-urethaneacrylate (SSQ-UA) copolymer films were prepared. CNFs-SSQ-UA nanocomposite films were highly transparent due to the filling of nanometer sized (10-20 nm) CNFs inside the hybrid organic-inorganic SSQ-UA copolymer. CNFs due to their crystalline structure drastically increased Young's moduli and the tensile strengths of the composite and decreased the thermal expansion. High thermal stability of polysilsesquioxane improved heat resistance of CNFs.

  4. Reinforcement of natural rubber latex with silica modified by cerium oxide:preparation and properties

    Institute of Scientific and Technical Information of China (English)

    张福全; 廖禄生; 王永周; 汪月琼; 黄红海; 李普旺; 彭政; 曾日中

    2016-01-01

    Variable masses of nano cerium oxide (CeO2) were added into nano silica (SiO2) to prepare the well-dispersed SiO2-CeO2 suspension (SiO2-CeO2), cetyltrimethyl ammonium bromide (CTAB) was used to adjust the compatibility of SiO2-CeO2 with rubber matrix, then SiO2-CeO2 modified by CTAB and curing formulas were mixed with fresh natural rubber (NR) latex to prepare NR/SiO2-CeO2 nanocomposites that contained 0–10 parts of CeO2 by a new emulsion compounding method. The morphologies, cure characteristics, mechanical properties and thermal-oxidative stability of NR/SiO2-CeO2 nanocomposites were investigated. The re-sults revealed that the presence of CeO2 in NR/SiO2-CeO2nanocomposites was favorable for enhancing the interaction between NR matrix and fillers, helped to get smaller SiO2-CeO2 particles with narrower particle size distribution, further improved the crosslink densities and mechanical properties of NR/SiO2-CeO2 nanocomposites vulcanizates. Meanwhile, the addition of CeO2 increased the active energy at least 4.66%, obviously improved the thermal-oxidative aging-inhibiting properties of NR/SiO2-CeO2 nanocomposites. Additionally, nanocomposites containing CeO2 promotedTg shift to high temperature direction, causing the nanocomposites featured higher tanδ at 0 ºC and lower tanδ at 60 ºC and exhibited comparable wet grip and lower rolling resistance when NR/SiO2-CeO2nano-composites were used in tire tread compound.

  5. Preparation and characterizations of naproxen-loaded magnetic nanoparticles coated with PLA- g-chitosan copolymer

    Science.gov (United States)

    Thammawong, C.; Sreearunothai, P.; Petchsuk, A.; Tangboriboonrat, P.; Pimpha, N.; Opaprakasit, P.

    2012-08-01

    Naproxen (NPX) drug-loaded magnetic nanoparticles (MNPs) have been prepared in a one-step process utilizing a biocompatible polylactide-grafted-chitosan copolymer. The copolymer serves both as a NPX drug carrier as well as a polymeric surfactant for the synthesis of MNPs without the use of any additional surfactant. Highly stable MNPs with high magnetization in the form of maghemite (γ-Fe2O3) are prepared in aqueous media. Effects of preparation conditions on structures and properties of the copolymer-coated and drug-loaded MNPs are investigated by employing particle size and zeta potential measurements, transmission electron microscopy, vibrating sample magnetometer, X-ray diffraction, Fourier-transform infrared, nuclear magnetic resonance, and confocal Raman spectroscopy. The results show that average particle size (150-300 nm), coating efficiency, and coating structures of the resulting MNPs materials are strongly dependent on MNP/copolymer and MNP/NPX ratios in feed. It is also observed that NPX acts as co-surfactant in the drug-loading process, resulting in different encapsulating structures with the variation in the MNP/copolymer and MNP/NPX ratios. Properties of the MNPs materials can be further optimized for use in specific biomedical applications.

  6. Preparation and characterizations of naproxen-loaded magnetic nanoparticles coated with PLA-g-chitosan copolymer

    Energy Technology Data Exchange (ETDEWEB)

    Thammawong, C.; Sreearunothai, P. [Thammasat University, School of Bio-Chemical Engineering and Technology, Sirindhorn International Institute of Technology (SIIT) (Thailand); Petchsuk, A. [National Metal and Materials Technology Center (MTEC) (Thailand); Tangboriboonrat, P. [Mahidol University, Department of Chemistry, Faculty of Science (Thailand); Pimpha, N. [National Nanotechnology Center (NANOTEC) (Thailand); Opaprakasit, P., E-mail: pakorn@siit.tu.ac.th [Thammasat University, School of Bio-Chemical Engineering and Technology, Sirindhorn International Institute of Technology (SIIT) (Thailand)

    2012-08-15

    Naproxen (NPX) drug-loaded magnetic nanoparticles (MNPs) have been prepared in a one-step process utilizing a biocompatible polylactide-grafted-chitosan copolymer. The copolymer serves both as a NPX drug carrier as well as a polymeric surfactant for the synthesis of MNPs without the use of any additional surfactant. Highly stable MNPs with high magnetization in the form of maghemite ({gamma}-Fe{sub 2}O{sub 3}) are prepared in aqueous media. Effects of preparation conditions on structures and properties of the copolymer-coated and drug-loaded MNPs are investigated by employing particle size and zeta potential measurements, transmission electron microscopy, vibrating sample magnetometer, X-ray diffraction, Fourier-transform infrared, nuclear magnetic resonance, and confocal Raman spectroscopy. The results show that average particle size (150-300 nm), coating efficiency, and coating structures of the resulting MNPs materials are strongly dependent on MNP/copolymer and MNP/NPX ratios in feed. It is also observed that NPX acts as co-surfactant in the drug-loading process, resulting in different encapsulating structures with the variation in the MNP/copolymer and MNP/NPX ratios. Properties of the MNPs materials can be further optimized for use in specific biomedical applications.

  7. Preparation and Characterization of Copolymer Micelles Formed by Poly(ethylene glycol)-Polylactide Block Copolymers as Novel Drug Carriers

    Institute of Scientific and Technical Information of China (English)

    姜维; 王运东; 甘泉; 张建铮; 赵秀文; 费维扬; 贝建中; 王身国

    2006-01-01

    Diblock copolymer poly(ethylene glycol) methyl ether-polylactide (MePEG-PLA) micelles were prepared by dialysis against water. Indomethacin (IMC) as a model drug was entrapped into the micelles by dialysis method. The critical micelle concentration (CMC) of the prepared micelles in distilled water investigated by fluorescence spectroscopy was 0.0051mg/mL which is lower than that of common low molecular weight surfactants. The diameters of MePEG-PLA micelles and IMC loaded MePEG-PLA micelles in a number-averaged scale measured by dynamic light scattering were 52.4 and 53.7 nm respectively. The observation with transmission electron microscope and scanning electron microscope showed that the appearance of MePEG-PLA micelles was in a spherical shape. The content of IMC incorporated in the core portion of the micelles was 18% (ω). The effects of the synthesis method of the copolymer on the polydispersity of the micelles and the yield of the micelles formation were discussed.

  8. Rheological behaviour of latexes in-can and during film drying

    NARCIS (Netherlands)

    Molenaar, F.; Svanholm, T.; Toussaint, A.

    1997-01-01

    In-can rheology was studied for sixteen model acrylate latexes and a commercial vinyl/acrylate copolymer latex. Following the model of Quemada, the shear thinning behaviour, the effects of latex neutralisation and the copolymer composition could be described. Furthermore, the rheological effects of

  9. Preparation of stimuli-responsive functionalized latex nanoparticles: the effect of spiropyran concentration on size and photochromic properties.

    Science.gov (United States)

    Abdollahi, Amin; Mahdavian, Ali Reza; Salehi-Mobarakeh, Hamid

    2015-10-06

    Incorporation of photochromic compounds to polymer matrix through chemical bonding results in an enhancement of photoactivity and stabilization of optical properties. Here, spiropyran ethyl acrylate monomer (SPEA) was synthesized, and then photochromic particles bearing epoxy functional groups were prepared through semicontinuous emulsion copolymerization. Dynamic light scattering (DLS) and scanning electron microscopy (SEM) results depicted an increase in particle size and particle size distribution with the increase in SPEA monomer-surfactants ratio. Studies on photochromic properties by UV-vis analysis demonstrated a decrease in the absorption intensity despite the increase in SPEA content due to the enhancement in particle size. The prepared acrylic copolymer particles showed reasonable photostability, photoreversibility, and fast photoresponsivness according to the convenient test methods under UV/vis irradiation. DSC and DMTA analyses indicate an increase in Tg of the obtained copolymers with the increase in SPEA content. Finally, stimuli-responsive cellulosic papers were prepared by impregnation, and their photochromic behavior was investigated in dry and wet forms in various media under UV radiation. Morphology studies, due to stabilization of the photochromic copolymer on cellulose fibers, were conducted by SEM micrographs and showed good adhesion and compatibility between the two phases.

  10. PREPARATION AND PERVAPORATION PROPERTIES OF PROPENE/1-DECENE COPOLYMER MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    Xiu-zhi Tian; Bao-ku Zhu; Xue Jiang; You-yi Xu

    2005-01-01

    Propene/1-decene copolymers (P-co-D) were synthesized by means of slurry polymerization process under atmospheric pressure using Ziegler-Natta catalyst (MgCl2/TiCl4/AlEt3). The random P-co-Ds were elastic, low-crystalline,thermally stable and therefore suitable to be used as membrane materials in organophilic pervaporation with chloroform/water mixture. Its mechanical strength is better than polydimethylsiloxane (PDMS). The correlation between structural parameters (glass transition temperature and crystallinity) and properties of organophilic pervaporation were investigated.

  11. Preparation of starch-sodium lignosulfonate graft copolymers via laccase catalysis and characterization of antioxidant activity

    Science.gov (United States)

    Graft copolymers of waxy maize starch and sodium lignosulfonate (SLS) were prepared by Trametes Versicolor laccase catalysis in aqueous solution. Amount of SLS grafted based on phenol analysis was 0.5% and 1.0% in the absence and presence of 1-hydroxybenzotriazole (HBT), respectively. Starch-SLS gra...

  12. Preparation of ethylene vinylalcohol copolymer membranes suitable for ligand coupling in affinity separation

    NARCIS (Netherlands)

    Avramescu, M.E.; Sager, W.F.C.; Mulder, M.H.V.; Wessling, Matthias

    2002-01-01

    Hydrophilic microfiltration membranes with functional groups that can be used as coupling sites for ligands are of central interest in affinity separation, especially in view of biomedical applications. In this study, we employed ethylene vinyl alcohol copolymer (EVAL) to prepare macrovoid-free open

  13. Block copolymers of styrene, isoprene, and ethylene oxide prepared by anionic polymerization. I. Synthesis and characterization

    NARCIS (Netherlands)

    Koetsier, D.W.; Bantjes, A.; Feijen, J.

    1978-01-01

    Anionic polymerization has been used as a technique for the synthesis of five-block copolymers of polystyrene (PS), polyisoprene (PI), and poly(ethylene oxide) (PEO). Two types of such polymers, PEO-PI-PS-PI-PEO and PEO-PS-PI-PS-PEO with varying PEO block length, have been prepared, using potassium

  14. Preparation of polystyrene-poly(ethylene glycol) diblock copolymer by "living" free radical polymerization

    DEFF Research Database (Denmark)

    Chen, Xianyi; Gao, Bo; Kops, Jørgen

    1998-01-01

    terminated with a TEMPO unit (MPEG-TEMPO), which was further used to prepare the diblock copolymer PS-b-PEG by 'living' free radical polymerisation of styrene. The product was purified and identified by H-1 n.m.r. and GPC. However, large amounts of homopolystyrene was also formed by simultaneous thermal...

  15. Block copolymers of styrene, isoprene, and ethylene oxide prepared by anionic polymerization. I. Synthesis and characterization

    NARCIS (Netherlands)

    Koetsier, D.W.; Bantjes, A.; Feijen, Jan

    1978-01-01

    Anionic polymerization has been used as a technique for the synthesis of five-block copolymers of polystyrene (PS), polyisoprene (PI), and poly(ethylene oxide) (PEO). Two types of such polymers, PEO-PI-PS-PI-PEO and PEO-PS-PI-PS-PEO with varying PEO block length, have been prepared, using potassium

  16. Ethylene-Octene Copolymers/Organoclay Nanocomposites: Preparation and Properties

    Directory of Open Access Journals (Sweden)

    Alice Tesarikova

    2016-01-01

    Full Text Available Two ethylene-octene copolymers with 17 and 45 wt.% of octene (EOC-17 and EOC-45 were compared in nanocomposites with Cloisite 93A. EOC-45 nanocomposites have a higher elongation at break. Dynamical mechanical analysis (DMA showed a decrease of tan⁡δ with frequency for EOC-17 nanocomposites, but decrease is followed by an increase for EOC-45 nanocomposites; DMA showed also increased modulus for all nanocomposites compared to pure copolymers over a wide temperature range. Barrier properties were improved about 100% by addition of organoclay; they were better for EOC-17 nanocomposites due to higher crystallinity. X-ray diffraction (XRD together with transmission electron microscopy (TEM showed some intercalation for EOC-17 but much better dispersion for EOC-45 nanocomposites. Differential scanning calorimetry (DSC showed increased crystallization temperature Tc for EOC-17 nanocomposite (aggregates acted as nucleation agents but decrease Tc for EOC-45 nanocomposite together with greatly influenced melting peak. Accelerated UV aging showed smaller C=O peak for EOC-45 nanocomposites.

  17. Preparation and characterization of polyethylene based graft copolymers. Applications in the immobilization of enzymes

    Science.gov (United States)

    Ferreira, L. M.; Rocha, J. M. S.; Andrade, M. E.; Gil, M. H.

    1998-06-01

    In the last few years new copolymeric supports for the immobilization of biological compounds have been developed. The graft copolymer polyethylene-g.co-hydroxyethyl methacrylate, partially hydrolyzed, has shown to be a very promising support for this purpose. The more recent work in the preparation and characterization of this copolymer, as well as the immobilization of a lipase, is reported in this paper. Branches of poly(hydroxyethyl methacrylate) were grafted onto low density polyethylene by using gamma radiation. The influence of the presence and absence of air, as well as the monomer concentration on the yield of grafting were evaluated. The obtained copolymers were characterized by DSC and FTIR. The influence of the support properties on the synthesis biocatalytic activity was detected.

  18. Cellulose-based graft copolymers prepared by simplified electrochemically mediated ATRP

    Directory of Open Access Journals (Sweden)

    P. Chmielarz

    2017-02-01

    Full Text Available Brush-shaped block copolymer with a dual hydrophilic poly(acrylic acid-block-poly(oligo(ethylene glycol acrylate (PAA-b-POEGA arms was synthesized for the first time via a simplified electrochemically mediated ATRP (seATRP under both constant potential electrolysis and constant current electrolysis conditions, utilizing only 30 ppm of catalyst complex. The polymerization conditions were optimized to provide fast reactions while employing low catalyst concentrations and preparation of cellulose-based brush-like copolymers with narrow molecular weight distributions. The results from proton nuclear magnetic resonance (1H NMR spectral studies support the formation of cellulose-based graft (copolymers. It is expected that these new polymer brushes may find application as pH- and thermo-sensitive drug delivery systems.

  19. Iron Oxide Arrays Prepared from Ferrocene- and Silsesquioxane-Containing Block Copolymers

    Directory of Open Access Journals (Sweden)

    Raita Goseki

    2012-01-01

    Full Text Available Arrays of iron oxides as precursors of iron clusters were prepared by oxygen plasma treatment of block copolymer microphase-separated nanostructures in thin films. Block copolymers composed of ferrocene-containing and silsesquioxane-containing polymethacrylate (PMAPOSS-b-PMAHFC were successfully prepared, with different molecular weights and compositions and narrow molecular weight distributions, by living anionic polymerization. The formed microphase-separated nanostructures in the bulk were characterized by wide- and small-angle X-ray scattering (WAXS and SAXS, scanning electron microscopy (SEM, and transmission electron microscopy (TEM. Thin films were prepared from a solution of PMAPOSS-b-PMAHFC in tetrahydrofuran by spin coating onto silicon wafers. Fingerprint-type line nanostructures were formed in the PMAPOSS-b-PMAHFCs thin films after solvent annealing with carbon disulfide. Oxygen plasma treatment provided the final line arrays of iron oxides based on the formed nanostructural patterns.

  20. Preparation and characterization of poly(acrylic acid)-hydroxyethyl cellulose graft copolymer.

    Science.gov (United States)

    Abdel-Halim, E S

    2012-10-01

    Poly(acrylic acid) hydroxyethyl cellulose [poly(AA)-HEC] graft copolymer was prepared by polymerizing acrylic acid (AA) with hydroxyethyl cellulose (HEC) using potassium bromate/thiourea dioxide (KBrO(3)/TUD) as redox initiation system. The polymerization reaction was carried out under a variety of conditions including concentrations of AA, KBrO(3) and TUD, material to liquor ratio and polymerization temperature. The polymerization reaction was monitored by withdrawing samples from the reaction medium and measuring the total conversion. The rheological properties of the poly(AA)-HEC graft copolymer were investigated. The total conversion and rheological properties of the graft copolymer depended on the ratio of KBrO(3) to TUD and on acrylic acid concentration as well as temperature and material to liquor ratio. Optimum conditions of the graft copolymer preparation were 30 mmol KBrO(3) and 30 mmol TUD/100g HEC, 100% AA (based on weight of HEC), duration 2h at temperature 50 °C using a material to liquor ratio of 1:10.

  1. Preparation and characterization of aqueous polyurethane oil/polyacrylate latex interpenetrating polymer network

    Science.gov (United States)

    Zhou, M. M.; Ma, L. L.; Du, J.; Cao, F.; Xiao, J. J.

    2015-07-01

    A series of aqueous polyurethane oil (network I)/polyacrylate (network II) latex interpenetrating polymer networks (LIPNs) were synthesized via the technology of latex interpenetrating polymer network combined seed emulsion polymerization process. Fourier transform infrared (FTIR) spectroscopy, laser particle size distributing analyzer and universal tension machine were utilized to characterize the bulk structures and mechanical properties of LIPNs. For used as damping material, the damping performance of LIPNs were analyzed by dynamic mechanical analysis (DMA). It was found that the damping temperature region of LIPN was wider than those of aqueous polyurethane oil, the temperature region with greater tanδ changed with the TPGDA content and hard-/soft-segment mass weight ratio (mMMA/mBA) and the glass transition temperature (Tg) of the network I and network II in LIPN occurred within shift each other, even overlap with increasing mMMA/mBA value. The results show that LIPNs synthesized through the combined process have greater tanδ and wider damping temperature region, which is suitable for the use of damping coatings.

  2. Radiation preparation of PVA/CMC copolymers and their application in removal of dyes

    Energy Technology Data Exchange (ETDEWEB)

    Taleb, Manal F. Abou, E-mail: abutalib_m@yahoo.com [National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Nasr City, P.O. Box 29, Cairo 11371 (Egypt); El-Mohdy, H. L. Abd; El-Rehim, H. A. Abd [National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Nasr City, P.O. Box 29, Cairo 11371 (Egypt)

    2009-08-30

    Copolymer hydrogels composed of poly(vinyl alcohol) (PVA) and carboxymethyl cellulose (CMC) was prepared by using electron beam irradiation as crosslinking agent. The copolymers were characterized by FTIR and the physical properties such as gelation. The thermal behavior and swelling properties of the prepared hydrogels were investigated as a function of PVA/CMC composition. The factors effecting adsorption capacity of acid, reactive and direct dyes onto PVA/CMC hydrogel, such as CMC content, pH value of the dye solution, initial concentration and adsorption temperature for dyes were investigated. Thermodynamic study indicated that the values the negative values of {Delta}H suggested that the adsorption process is exothermic. The value of {Delta}H (38.81 kJ/mol) suggested that the electrostatic interaction is the dominant mechanism for the adsorption of dyes on hydrogel.

  3. PREPARATION AND APPLICATION OF COPOLYMERS OF 2-ACRYLAMIDO-2-METHYL PROPANE SULFO ACID AS WASTE WATER TREATMENT AGENTS

    Institute of Scientific and Technical Information of China (English)

    FushanChen; HongjieZhang; HuirenHu; QiushiHe

    2004-01-01

    In this paper, the preparation and application of copolymers of 2-acrylamido-2-methyl propane sulfo acid (AMPS) were discussed. The results showed that the copolymers with molecular weight 18.10 million can be prepared. In treating waste water from deinked pulp, the dosage of copolymers was 0.75ppm, the optimum dosage of PAC was 100ppm; dosage of the amphoteric polyacylamide (AmPAM) with molecular weight 11.34 million was 0.75ppm, the optimum dosage of PAC was 75ppm. Theremoved rate of CODcr was above 70%.

  4. Synthesis and Characterization of All-Conjugated Block Copolymers Prepared via Click Chemistry

    Science.gov (United States)

    Verduzco, Rafael; Smith, Kendall

    2012-02-01

    All-conjugated block copolymers with both hole-conducting and electron-conducting polymer blocks can be used to address fundamental questions regarding the structure, optoelectronic properties, and photovoltaic performance of organic photovoltaic blends, but synthetic challenges have precluded comprehensive studies on such systems. Here, we present a novel synthetic approach for preparing all-conjugated block copolymers and detailed studies of their nanoscale structure and optical properties. Our synthetic approach is based on copper-catalyzed azide-alkyne ``click'' chemistry and enables us to prepare block copolymers with a poly(3-alkylthiophene) block covalently linked to a conjugated polymer prepared by Suzuki polycondensation polymerization, including poly(9,9-dioctyl fluorene), poly(9,9-dioctyl fluorene-alt-benzothiadiazole) and poly((9,9-dioctylfluorene)-2,7-diyl-alt-[4,7-bis(thiophen-5-yl)-2,1,3-benzothiadiazole]-2',2''-diyl) (PFOTBT). A combination of x-ray diffraction, grazing-incidence x-ray scattering, atomic force microscopy, and fluorescence quenching measurements give insight into their microstructure and potential for use in high-performance all-polymer photovoltaics.

  5. Practical Latex

    CERN Document Server

    Grätzer, George

    2014-01-01

    Accessible at 200+ pages to all who want to learn the practical usages of LaTeX Avoids technical subjects like font usage Friendly and easy to read, with many examples included Extra source materials include sample LaTeX files and suggestions for further reading

  6. STUDIES ON POLYSILOXANE-POLYSTYRENE COMPOSITE LATEXES

    Institute of Scientific and Technical Information of China (English)

    HUANG Ying; LIU Xianglian; YU Yunzhao

    1994-01-01

    Polysiloxane-polystyrene composite latexes were prepared by two-stage emulsion polymerization. Polymerization of styrene in swollen polysiloxane latex particles were studied.Formation of simple polystyrene particle in the 2nd-stage polymerization depends on the particle size of the 1st-stage latex and the polymerization temperature. Polystyrene domains in the vulcanizates reinforce the silicone rubbers effectively.

  7. Chitosan-graft poly(p-dioxanone) copolymers: preparation, characterization, and properties.

    Science.gov (United States)

    Wang, Xiu-Li; Huang, Yan; Zhu, Jiang; Pan, Yan-Bo; He, Rui; Wang, Yu-Zhong

    2009-04-21

    A new biodegradable copolymer of chitosan and poly(p-dioxanone) (PPDO) was prepared through a protection-graft-deprotection procedure using N-phthaloyl-chitosan as an intermediate. PPDO terminated with the isocyanate group was allowed to react with hydroxyl groups of the N-phthaloyl-protected chitosan, and then the phthaloyl group was cleaved to give the free amino groups. The length of PPDO graft chains can be controlled easily by using the prepolymers of PPDO with different molecular weights. The resulting products were thoroughly characterized with FT-IR, (1)H NMR, TG, DSC, SEM, and WAXD. The copolymers were used as drug carriers for sinomenine (7,8-didehydro-4-hydroxy-3,7-dimethoxy-17-methyl-9alpha,13alpha,14alpha-morphinan-6-one) and these exhibited a significant controlled drug-releasing behavior whether in artificial gastric juice or in neutral phosphate buffer solution.

  8. Preparation and characterization of star ABC triblock copolymer of ethylene oxide,styrene and methyl methacrylate

    Institute of Scientific and Technical Information of China (English)

    黄骏廉; 黄晓宇; 胡文兵; 楼文奎

    1997-01-01

    A universally significant method,which combines the anionic polymerization with photoinduced charge transfer polymerization,for preparation of soluble star ABC triblock copolymer of ethylene oxide,styrene and methyl methacrylate,was described.The poly(ethylene oxide) (PEO) block was formed by initiation of phenoxy an-ions using p-aminophenol protected by Schiff’s base as the parent compound Then the charge transfer system composed of PEO chains with deprotected-amino end groups and benzophenone initiated the polymerization of styrene and methyl metnacrylate sequentially under UV irradiation.The formed star triblock copolymer of styrene,ethylene oxide and methyl methacrylate could be purified by thin-layer chromatography (TLC) and characterized by IR,1H NMR,GPC (gel permeation chromatogrphy) and PGC (pyrolysis gas chromatography).

  9. Preparation of stable spherical micelles with rigid backbones based on polyaryletherketone copolymers containing lateral pyridyl groups

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Shuling; Liu, Lingzhi; Guo, Yunliang; Jiang, Zhenhua; Wang, Guibin, E-mail: wgb@jlu.edu.cn

    2013-07-15

    A new bisphenol monomer, 3-(3,4-dihydroxyphenylimine) pyridine (PYPH), was synthesized via a deoxidization reaction of an amine. A series of novel polyaryletherketone copolymers containing lateral pyridyl groups (PY-PAEKs) based on PYPH, 2,2-di(4-hydroxyphenyl)propane and 4,4′-difluorobenzophenone were prepared by nucleophilic aromatic substitution polycondensation reactions. Furthermore, spherical micelles with rigid PY-PAEKs as the inner cores and flexible polyacrylic acid (PAA) as the outer shells were obtained in a selective solvent (H{sub 2}O) successfully. The formation of the spherical micelles was confirmed by scanning electron and transmission electron microscopy as well as by surface tension measurements. The formation and size of the spherical micelles depended on the weight ratio of PAA/PY-PAEK, the concentration and pH value of the mixed solution containing the PY-PAEK and PAA, and the number of pyridyl groups in the PY-PAEK. The structure of the spherical micelles could be stabilized by a cross-linking reaction between the pyridyl groups of the PY-PAEKs and 1,4-dibromobutane. The diameter of the spherical micelles decreased because of the removal of the PAA shell from the PY-PAEK core after the cross-linking reaction. The resulting stable spherical micelles with rigid backbones did not dissolve in a number of polar solvents and remained unaffected by changes in the pH values. - Graphical abstract: Display Omitted - Highlights: • Polyaryletherketone copolymers containing lateral pyridyl groups were synthesized. • Spherical micelles were prepared using these copolymers and polyacrylic acid. • The copolymers and polyacrylic acid formed the core and the shell of the micelles, respectively. • The obtained micelles were stabilized by a cross-linking reaction. • The cross-linked micelles had rigid backbones, independent of solvents and pH values.

  10. Preparation of CO₂/N₂-triggered reversibly coagulatable and redispersible polyacrylate latexes by emulsion polymerization using a polymeric surfactant.

    Science.gov (United States)

    Zhang, Qi; Yu, Guoqiang; Wang, Wen-Jun; Li, Bo-Geng; Zhu, Shiping

    2012-05-29

    We report here a novel approach for making reversibly coagulatable and redispersible polyacrylate latexes by emulsion (co)polymerization of methyl methacrylate (MMA) using a polymeric surfactant, poly(2-(dimethylamino)ethyl methacrylate)(10) -block-poly(methyl methacrylate)(14) . The surfactant was protonated with HCl prior to use. The resulted PMMA latexes were readily coagulated with trace amount of caustic soda. The coagulated latex particles, after washing with deionized water, could be redispersed into fresh water to form stable latexes again by CO(2) bubbling with ultrasonication. The recovered latexes could then be coagulated by N(2) bubbling with gentle heating. These coagulation and redispersion processes were repeatable by the CO(2) /N(2) bubbling.

  11. Preparation, blood coagulation and cell compatibility evaluation of chitosan-graft-polylactide copolymers.

    Science.gov (United States)

    Wang, Qi; Liu, Pei; Liu, Peifeng; Gong, Tao; Li, Suming; Duan, Yourong; Zhang, Zhirong

    2014-02-01

    Biodegradable chitosan-graft-polylactide (PLA-CS) copolymers were prepared by the grafting of a poly(L-lactide) (PLLA) or poly(D-lactide) (PDLA) precursor to the backbone of chitosan using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC ⋅ HCl) and N-hydroxysuccinimide (NHS) as a coupling agent. The blood and cell compatibility of the graft copolymers were investigated in comparison to PLLA and PDLA homopolymers. The coagulation properties of PLA-CS were evaluated by hemolysis, plasma recalcification, dynamic blood clotting and protein absorption assays. PLA-CS copolymers present similar hemolysis ratio and plasma recalcification time as PLA, but slower dynamic blood clotting and lower protein absorption. The cell viability was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), agar diffusion and lactate dehydrogenase (LDH) experiments. All the samples presented no effect on the viability to cells. Inflammatory cytokine analysis using sandwich ELISAs revealed that PLA-CS would not stimulate inflammatory activity.

  12. Preparation of anionically polymerized butadiene-co-styrene copolymer-multiwalled carbon nanotubes nanocomposites

    Institute of Scientific and Technical Information of China (English)

    Zhong Guang; Wang, Jing Hua; Ling Xu

    2012-01-01

    Poly(butadiene-co-styrene) copolymer/multi-walled carbon nanotubes (SB-MWNTs) nanocomposites are prepared via terminating anionically synthesized living poly(butadiene-styryl)lithium with acyl chlorides on the MWNTs,which obtained from the carboxylation and acylation of the MWNTs.Results from the characterization of the SB-MWNTs nanocomposites,including its soluble in solvent,UV-vis and TEM of the dissolved samples,TGA and SEM of nanocomposites are presented and discussed respectively.MWNTs treated by SB can be easily distributed in the SBR (styrene-butadiene rubber) matrix.

  13. Colloid stable sorbents for cesium removal: preparation and application of latex particles functionalized with transition metals ferrocyanides.

    Science.gov (United States)

    Avramenko, Valentin; Bratskaya, Svetlana; Zheleznov, Veniamin; Sheveleva, Irina; Voitenko, Oleg; Sergienko, Valentin

    2011-02-28

    In this paper we suggest a principally new approach to preparation of colloid stable selective sorbents for cesium uptake using immobilization of transition metals (cobalt, nickel, and copper) ferrocyanides in nanosized carboxylic latex emulsions. The effects of ferrocyanide composition, pH, and media salinity on the sorption properties of the colloid stable sorbents toward cesium ions were studied in solutions containing up to 200 g/L of sodium nitrate or potassium chloride. The sorption capacities of the colloid sorbents based on mixed potassium/transition metals ferrocyanides were in the range 1.3-1.5 mol Cs/mol ferrocyanide with the highest value found for the copper ferrocyanide. It was shown that the obtained colloid-stable sorbents were capable to penetrate through bulk materials without filtration that made them applicable for decontamination of solids, e.g. soils, zeolites, spent ion-exchange resins contaminated with cesium radionuclides. After decontamination of liquid or solid radioactive wastes the colloid-stable sorbents can be easily separated from solutions by precipitation with cationic flocculants providing localization of radionuclides in a small volume of the precipitates formed.

  14. Colloid stable sorbents for cesium removal: Preparation and application of latex particles functionalized with transition metals ferrocyanides

    Energy Technology Data Exchange (ETDEWEB)

    Avramenko, Valentin [Institute of Chemistry, Far Eastern Branch, Russian Academy of Sciences, 159 ave 100-letiya Vladivostoka, Vladivostok 690022 (Russian Federation); Bratskaya, Svetlana, E-mail: sbratska@ich.dvo.ru [Institute of Chemistry, Far Eastern Branch, Russian Academy of Sciences, 159 ave 100-letiya Vladivostoka, Vladivostok 690022 (Russian Federation); Zheleznov, Veniamin; Sheveleva, Irina [Institute of Chemistry, Far Eastern Branch, Russian Academy of Sciences, 159 ave 100-letiya Vladivostoka, Vladivostok 690022 (Russian Federation); Voitenko, Oleg [Far Eastern Federal University, Laboratory of Electron Microscopy and Image Processing, 27, Oktyabr' skaya Street, Vladivostok 690950 (Russian Federation); Sergienko, Valentin [Institute of Chemistry, Far Eastern Branch, Russian Academy of Sciences, 159 ave 100-letiya Vladivostoka, Vladivostok 690022 (Russian Federation)

    2011-02-28

    In this paper we suggest a principally new approach to preparation of colloid stable selective sorbents for cesium uptake using immobilization of transition metals (cobalt, nickel, and copper) ferrocyanides in nanosized carboxylic latex emulsions. The effects of ferrocyanide composition, pH, and media salinity on the sorption properties of the colloid stable sorbents toward cesium ions were studied in solutions containing up to 200 g/L of sodium nitrate or potassium chloride. The sorption capacities of the colloid sorbents based on mixed potassium/transition metals ferrocyanides were in the range 1.3-1.5 mol Cs/mol ferrocyanide with the highest value found for the copper ferrocyanide. It was shown that the obtained colloid-stable sorbents were capable to penetrate through bulk materials without filtration that made them applicable for decontamination of solids, e.g. soils, zeolites, spent ion-exchange resins contaminated with cesium radionuclides. After decontamination of liquid or solid radioactive wastes the colloid-stable sorbents can be easily separated from solutions by precipitation with cationic flocculants providing localization of radionuclides in a small volume of the precipitates formed.

  15. Preparation and application of nanocrystalline cellulose derived from sugarcane waste as filler modified alkanolamide on crosslink of natural rubber latex film

    Science.gov (United States)

    Harahap, Hamidah; Hayat, Nuim; Lubis, Marfuah

    2017-07-01

    Sugarcane waste is abundant sources of cellulose and it has potential to reutilize. Cellulose from sugarcane waste can be derived into nanocystalline cellulose (NCC) from crystalline region. The NCC as a filler has capability to reinforce natural rubber latex product. The crosslink in vulcanized natural rubber latex film influences several properties of product. In this work, we extracted NCC from sugarcane waste then added into natural rubber latex as filler modified alkanolamide (ALK) and also studied the crosslink of natural rubber latex films. NCC were produced from sugarcane waste by hydrolysis process with sulfuric acid 45%. The obtained NCC was characterized by using x-ray diffraction (XRD), transmission electron microscopy (TEM), and fourier transform infra red (FTIR). NCC was modified by alkanolamide and dispersed in water with filler concentration of 10%. Then the dispersion were added into latex system followed by pre-vulcanization at 70 °C. The films were prepared by coagulant dipping method and dried at 100 °C and 120 °C for 20 minutes. Characterization of NCC from sugarcane waste by using FTIR was done, it clearly showed the functional groups of cellulose. TEM showed the obtained NCC were rod-shaped with about 40-160 nm in diameter and several hundred nm in length, and XRD showed that the degree of crystalinity of NCC from sugarcane waste is 92.33%. The crosslink of natural rubber films were studied by measure the crosslink density for different filler loading by using swelling measurement with toluene solution. The result show that the crosslink density increased in line with amount of filler which added into the system, and also the crosslink density that obtained from vulcanization at 120 °C were higher than 100 °C.

  16. Preparation of pH-responsive membranes with amphiphilic copolymers by surface segregation method☆

    Institute of Scientific and Technical Information of China (English)

    Yanlei Su; Yuan Liu; Xueting Zhao; Yafei Li; Zhongyi Jiang

    2015-01-01

    Novel pH-responsive membranes were prepared by blending pH-responsive amphiphilic copolymers with pol-yethersulfone (PES) via a nonsolvent-induced phase separation (NIPS) technique. The amphiphilic copolymers bearing Pluronic F127 and poly(methacrylic acid) (PMAA) segments, abbreviated as PMAAn–F127–PMAAn, were synthesized by free radical polymerization. The physical and chemical properties of the blend membranes were evaluated by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectrum, water con-tact angle, Zeta potential and X-ray photoelectron spectroscopy (XPS). The enrichment of hydrophilic PMAA seg-ments on the membrane surfaces was attributed to surface segregation during the membrane preparation process. The blend membranes had significant pH-responsive properties due to the conformational changes of surface-segregated PMAA segments under different pH values of feed solutions. Fluxes of the blend membranes were larger at low pH values of feed solutions than that at high pH values. The pH-responsive ability of the mem-branes was enhanced with the increase of the degree of PMAA near-surface coverage.

  17. Preparation,structure and properties of PP-g-AA grafting copolymer

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Polypropylene grafting with AA was prepared by reactive extrusion with pre-irradiated PP (rPP) as the homogeneous initiator.The effects of the pre-irradiated dose,the fraction of rPP and the concentration of acrylic acid on the grafting reaction were studied and the grafted PP was characterized by Fourier transition infrared spectroscopy (FTIR),differential scanning calorimeter (DSC)and polarized light microscopy (PLM).The results show that the degradation of PP was suppressed efficiently with this novel method for preparing PP-g-AA copolymers,and the grafted copolymers with good mechanical properties were obtained.It was found that the product with higher graft degree (Gd)(0.19%) and relatively excellent mechanical properties can be produced if the mass ratio of PP/rPP/AA 4 kGy.Moreover,an adhesive strength of 4.88 kN/m was reached in the PP-g-AA/aluminum laminate.

  18. Preparation of hydrophilic vinyl chloride copolymer hollow fiber membranes with antifouling properties

    Science.gov (United States)

    Rajabzadeh, Saeid; Sano, Rie; Ishigami, Toru; Kakihana, Yuriko; Ohmukai, Yoshikage; Matsuyama, Hideto

    2015-01-01

    Hydrophilic vinyl chloride copolymer hollow fiber membranes with antifouling properties were prepared from brominated vinyl chloride-hydroxyethyl methacrylate copolymer (poly(VC-co-HEMA-Br)). The base membrane was grafted with two different zwitterionic monomers, (2-methacryloyloxyethylphosphorylcholine) (MPC) and [2-(methacryloyloxy) ethyl] dimethyl (3-sulfopropyl) ammonium hydroxide) (MEDSAH), and poly(ethylene glycol) methyl ether methacrylate (PEGMA). The effect of the grafting on the base membrane hydrophilicity and antifouling properties was investigated. For comparison of the results, the pure water permeabilities and pore sizes at the outer surfaces of the grafted hollow fiber membranes were controlled to be similar. A poly(VC-co-HEMA-Br) hollow fiber membrane with similar pure water permeability and pore size was also prepared as a control membrane. A BSA solution was used as a model fouling solution for evaluation of the antifouling properties. Grafting with zwitterionic monomers and PEGMA improved the antifouling properties compared with the control membrane. The PEGMA grafted membrane showed the best antifouling properties among the grafted membranes

  19. Highly conductive poly(methyl methacrylate) (PMMA)-reduced graphene oxide composite prepared by self-assembly of PMMA latex and graphene oxide through electrostatic interaction.

    Science.gov (United States)

    Pham, Viet Hung; Dang, Thanh Truong; Hur, Seung Hyun; Kim, Eui Jung; Chung, Jin Suk

    2012-05-01

    We report a simple, environmentally friendly approach for preparing highly conductive poly(methyl methacrylate)-reduced graphene oxide (PMMA-RGO) composites by self-assembly of positively charged PMMA latex particles and negatively charged graphene oxide sheets through electrostatic interactions, followed by hydrazine reduction. The PMMA latex was prepared by surfactant-free emulsion polymerization using a cationic free radical initiator, which created the positive charges on the surface of the PMMA particle. By mixing PMMA latex with a graphene oxide dispersion, positively charged PMMA particles easily assembled with negatively charged graphene oxide sheets through electrostatic interaction. The obtained PMMA-RGO exhibited excellent electrical properties with a percolation threshold as low as 0.16 vol % and an electrical conductivity of 64 S/m at only 2.7 vol %. Moreover, the thermomechanical properties of PMMA-RGO were also significantly improved. The storage modulus of PMMA-RGO increased by about 30% at 4.0 wt % RGO at room temperature while the glass transition temperature of PMMA-RGO increased 15 °C at only 0.5 wt % RGO.

  20. PREPARATION AND APPLICATION OF COPOLYMERS OF 2-ACRYLAMIDO-2-METHYL PROPANE SULFO ACID AS WASTE WATER TREATMENT AGENTS

    Institute of Scientific and Technical Information of China (English)

    Fushan Chen; Hongjie Zhang; Huiren Hu; Qiushi He

    2004-01-01

    In this paper, the preparation and application ofcopolymers of 2-acrylamido-2-methyl propane sulfoacid (AMPS) were discussed. The results showed thatthe copolymers with molecular weight 18.10 millioncan be prepared. In treating waste water fromdeinked pulp, the dosage of copolymers was0.75ppm, the optimum dosage of PAC was 100ppm;dosage of the amphoteric polyacylamide (AmPAM)with molecular weight 11.34 million was 0.75ppm,the optimum dosage of PAC was 75ppm. Theremoved rate of CODcr was above 70%.

  1. Sulfonate-containing Copolymers Prepared by Semi-Continuous Emulsion Copolymerizaiton of Styrene and Sodium Styrene Sulfonate

    Institute of Scientific and Technical Information of China (English)

    Shiming HUANG; Wei XIE; Chengyou KAN; Yajie LI; Deshan LIU

    2005-01-01

    @@ 1Introduction Soap-free emulsion copolymerization of styrene (St) and sodium sulfonate styrene (NaSS) could yield homodisperse sulfonate-containing particles with clean surface. But the incorporation of NaSS could never be increased beyond 2.6 % by weight in the conventional batch and seeded emulsion copolymerization in the absence of emulsifier because large amounts of soluble polyelectrolyte would unstablize the reaction system if excessive amount of NaSS was used[1]. In our work, semi-continuous copolymerizations were carried out in the presence of mixed emulsifiers, and a new method to purify the latex polymer was developed. The influences of the NaSS mole ratio in the total monomers and the monomer addition time on the S content in the purified copolymer were investigated by elemental analysis.

  2. Preparation and Characterization of Nimodipine-loaded Methoxy Poly (ethylene glycol)-poly (lactic acid) Diblock Copolymer Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHA Liu-sheng; LI Lan; ZHAO Hui-peng

    2006-01-01

    Amphiphilic diblock copolymers, methoxy poly (ethylene glycol)-poly(lactic acid) (MePEG-PLA), were synthesized from monomers of DL-lactide and methoxy poly (ethylene glycol) by a ring opening bulk polymerization in the presence of stannous octoate. Their chemical structure and physical properties were investigated using FTIR, NMR, GPC, and fluorescence spectroscopy. To estimate the feasibility as colloidal drug carrier, nimodipine (ND) was loaded into MePEG-PLA block copolymer nanoparticles by phaseseparation/dialysis method. The mean diameter and drug loading efficiency of ND-loaded MePEG-PLA copolymer nanoparticles depended on PLA/MePEG block composition of the copolymer and drug/polymer feed ratio in preparation. NMR study confirmed that nimodipine was entrapped into the hydrophobic inner core of MePEG-PLA copolymer nanoparticles and hydrophilic PEG chains were located on the surface of the drug-loaded polymer nanoparticles. In vitro release experiments exhibited the sustained release behavior of nimodipine from MePEG-PLA copolymer nanoparticles, without any burst effect.

  3. Highly protein-resistant coatings and suspension cell culture thereon from amphiphilic block copolymers prepared by RAFT polymerization.

    Science.gov (United States)

    Haraguchi, Kazutoshi; Kubota, Kazuomi; Takada, Tetsuo; Mahara, Saori

    2014-06-09

    Novel amphiphilic block copolymers composed of hydrophobic (poly(2-methoxyethyl acrylate): M) and hydrophilic (poly(N,N-dimethylacrylamide): D) segments were synthesized by living radical polymerization: a reversible addition-fragmentation chain-transfer polymerization. Two types of amphiphilic block copolymers, triblock (MDM) and 4-arm block ((MD)4) copolymers with specific compositions (D/M = (750-1500)/250), were prepared by a versatile one-pot synthesis. These copolymers show good adhesion to various types of substrates (e.g., polystyrene, polycarbonate, polypropylene, Ti, and glass), and the surface coating showed high protein repellency and a low contact angle for water, regardless of the substrate. The two opposing characteristics of high protein repellency and good substrate adhesion were achieved by the combined effects of the molecular architecture of the block copolymers, the high molecular weight, and the characteristics of each segment, that is, low protein adsorption capability of both segments and low glass transition temperature of the hydrophobic segment. Further, a polystyrene dish coated with the MDM block copolymer could be sterilized by γ-ray irradiation and used as a good substrate for a suspension cell culture that exhibits low cell adhesion and good cell growth.

  4. Microspheres for protein delivery prepared from amphiphilic multiblock copolymers. 1. influence of preparation techniques on particle characteristics and protein delivery

    NARCIS (Netherlands)

    Bezemer, J.M.; Radersma, R.; Grijpma, Dirk W.; Dijkstra, Pieter J.; van Blitterswijk, Clemens; Feijen, Jan

    2000-01-01

    The entrapment of lysozyme in amphiphilic multiblock copolymer microspheres by emulsification and subsequent solvent removal processes was studied. The copolymers are composed of hydrophilic poly(ethylene glycol) (PEG) blocks and hydrophobic poly(butylene terephthalate) (PBT) blocks. Direct solvent

  5. Polystyrene latex particles containing europium complexes prepared by miniemulsion polymerization using bovine serum albumin as a surfactant for biochemical diagnosis.

    Science.gov (United States)

    Aikawa, Tatsuo; Mizuno, Akihiro; Kohri, Michinari; Taniguchi, Tatsuo; Kishikawa, Keiki; Nakahira, Takayuki

    2016-09-01

    Luminescent particles have been attracting significant attention because they can be used in biochemical applications, such as detecting and imaging biomolecules. In this study, luminescent polystyrene latex particles were prepared through miniemulsion polymerization of styrene with dissolved europium complexes in the presence of bovine serum albumin (BSA) and poly(ethylene glycol) monomethoxy methacrylate as surfactants. The solubility of the europium complex in styrene has a strong effect on the yield of the particle. Europium tris(2-thenoyl trifluoroacetonate) di(tri-n-octyl phosphine oxide), which has a high solubility in styrene, was sufficiently incorporated into the polystyrene particles compared to europium tris(2-thenoyl trifluoroacetonate), which has a low solubility in styrene. The luminescence property of the europium complex could remain intact even after its incorporation through the miniemulsion polymerization. In the aqueous dispersion, the resulting particles could emit strong luminescence, which is a characteristic of the europium complex. The antibody fragments were covalently attached to BSA-covered particles after a reaction with a bifunctional linker, N-(6-maleimidocaproyloxy)succinimide. The time-resolved fluoroimmunoassay technique showed that 3.3pg/mL of human α-fetoproteins (AFP) can be detected by using the resulting luminescent particles. An immunochromatographic assay using the resulting particles was also performed as a convenient method to qualitatively detect biomolecules. The detection limit of AFP measured by the immunochromatographic assay was determined to be 2000pg/mL. These results revealed that the luminescent particles obtained in this study can be utilized for the highly sensitive detection of biomolecules and in vitro biochemical diagnosis.

  6. Co-coagulation of the NBR latex and clay aqueous suspension: preparation and characterization;Co-coagulacao de latex de NBR e suspensao aquosa de argila: preparacao e caracterizacao

    Energy Technology Data Exchange (ETDEWEB)

    Reis, Raquel S.; Brum, Elisson; Silva, Vanessa M. [Nitriflex S/A Industria e Comercio, Rio de Janeiro, RJ (Brazil); Souza, Diego H.S.; Gomes, Ailton de S.; Nunes, Regina C.R., E-mail: rcnunes@ima.ufrj.b [Universidade Federal do Rio de Janeiro (IMA/UFRJ), RJ (Brazil). Inst. de Macromoleculas Profa. Eloisa Mano

    2009-07-01

    Blends of nitrile rubber (NBR) and sodium montmorillonite (MMT-Na) were prepared by co-coagulation of the NBR latex with aqueous suspension of clay. The content of MMT was varied from 0 to 7 phr and different mixtures were analyzed by X-ray diffraction, light scattering, gel content, thermogravimetric analysis and the oscillating disk rheometer. The different methods used indicated that there was formation of a structure interspersed in the mixtures studied, and that increasing the content MMT-Na enhances the values obtained. Rheological measurements on compositions with NBR showed the influence of clay on increasing the time of healing in terms of its content, as is the gel content and the thermal resistance. All results were compared to composition of NBR without MMT. (author)

  7. Preparation of amorphous aluminum oxide-hydroxide nanoparticles in amphiphilic silicone-based copolymer microemulsions.

    Science.gov (United States)

    Berkovich, Yana; Aserin, Abraham; Wachtel, Ellen; Garti, Nissim

    2002-01-01

    Organo-inorgano nanocomposites with colloidal dimensions have interesting optical, catalytic, and mechanical properties, particularly when such hybrids are reinforced with transition metal oxide nanoparticles. Nanoparticles with a mean size of 1.0-2.4 nm are obtained through hydrolysis of aluminum isopropoxide in the L(2) phase of amphiphilic (PDMS-POE) polydimethylsiloxane-polyoxyethylene Silwet L-7607-octanol/acetylacetone-water mixtures. The particle sizes are related weakly to the microemulsion composition: 0.8-1.2 nm for 20 wt% Silwet L-7607 and 2.0-2.4 nm for 50 wt% Silwet L-7607. Protection of the particles against aggregation is ensured through their confinement in the intraaggregate colloidal domains. Factors affecting the hydrolysis-condensation process of acetylacetone-complexed aluminum isopropoxide in copolymer-poor and copolymer-rich regions of PDMS-POE W/O microemulsions are studied by Fourier transform infrared spectroscopy, small angle X-ray scattering, and transmission electron microscopy. Prepared nanoparticulate dispersions possess long-term stability and form clear mixtures in different organic polar and nonpolar solvents.

  8. Hg(II) adsorption using amidoximated porous acrylonitrile/itaconic copolymers prepared by suspended emulsion polymerization.

    Science.gov (United States)

    Ji, Chunnuan; Qu, Rongjun; Chen, Hou; Liu, Xiguang; Sun, Changmei; Ma, Caixia

    2016-01-01

    Initially, porous acrylonitrile/itaconic acid copolymers (AN/IA) were prepared by suspended emulsion polymerization. Successively, the cyano groups in AN/IA copolymers were converted to amidoxime (AO) groups by the reaction with hydroxylamine hydrochloride. The structures of the AN/IA and amidoximated AN/IA (AO AN/IA) were characterized by infrared spectroscopy, scanning electron microscopy, and porous structural analysis. The adsorption properties of AO AN/IA for Hg(II) were investigated. The results show that AO AN/IA has mesopores and macropores, and surface area of 11.71 m(2) g(-1). It was found that AO AN/IA has higher affinity for Hg(II), with the maximum adsorption capacity of 84.25 mg g(-1). The AO AN/IA also can effectively remove Hg(II) from different binary metal ion mixture systems. Furthermore, the adsorption kinetics and thermodynamics were studied in detail. The adsorption equilibrium can quickly be achieved in 4 h determined by an adsorption kinetics study. The adsorption process is found to belong to the second-order model, and can be described by the Freundlich model.

  9. Low-dielectric, nanoporous polyimide thin films prepared from block copolymer templating

    Directory of Open Access Journals (Sweden)

    C. Wang

    2013-08-01

    Full Text Available In this paper, a new method to the preparation of low-dielectric nanoporous polyimide (PI films was addressed, based on the self-assembly structures of PS-b-P4VP/poly(amic acid (PAA, precursor of PI blends. It is found the microphase-separation structure of PS-b-P4VP/PAA is a precondition of the formation of nanoporous structures, which could be achieved by solvent annealing. Nanoporous PI films with spherical pore size of ~11 nm were obtained by thermal imidization followed by the removal of the PS-b-P4VP block copolymer. The porosity of the nanoporous PI films could be controlled by the weight fraction of the PS-b-P4VP block copolymer. The dielectric properties of the nanoporous PI films were studied, and it was found that the introduction of nanopores could effectively reduce the dielectric constant from 3.60 of dense PI films to 2.41 of nanoporous PI films with a porosity of 26%, making it promising in microelectronic devices. The fabrication method described here could be extended to other polymer systems.

  10. Latex Allergy

    Science.gov (United States)

    ... nav nav, .header-9#header-section #main-nav, #overlay-menu nav, #mobile-menu, #one-page-nav li . ... bandagesDiapers and sanitary padsCondomsIn addition, many medical and dental supplies contain latex, including gloves, blood pressure cuffs, ...

  11. Properties of Starch-Poly(acrylamide-co-2-acrylamido-2-methylpropanesulfonic acid) Graft Copolymers Prepared by Reactive Extrusion

    Science.gov (United States)

    Graft copolymers of starch with acrylamide and 2-acrylamido-2-methylpropanesulfonic acid (AMPS) were prepared by reactive extrusion in a twin-screw extruder. The weight ratio of total monomer to starch was fixed at 1:3, while the molar fraction of AMPS in the monomer feed ranged from 0 to 0.119. Mon...

  12. Preparation and physical properties of enhanced radiation induced crosslinking of ethylene-vinyl alcohol copolymer (EVOH)

    Energy Technology Data Exchange (ETDEWEB)

    Deng Pengyang [Changchun Institute of Applied chemistry, Chinese Academy of Science, 5625 Renmin Street, Changchun, Jilin 130022 (China) and Graduate School of Chinese Academy of Science, 19 Yuquan Street, Beijing 100039 (China)]. E-mail: dpyang@ciac.jl.cn; Liu Meihua [Changchun Institute of Applied chemistry, Chinese Academy of Science, 5625 Renmin Street, Changchun, Jilin 130022 (China); Department of Materials Science and Engineering, Jilin University, 142 Renmin Street, Changchun, Jilin 130025 (China); Zhang Wanxi [Department of Materials Science and Engineering, Jilin University, 142 Renmin Street, Changchun, Jilin 130025 (China); Sun Jiazhen [Changchun Institute of Applied chemistry, Chinese Academy of Science, 5625 Renmin Street, Changchun, Jilin 130022 (China)

    2007-05-15

    Preparation and physical properties of ethylene-vinyl alcohol copolymer (EVOH) crosslinked by enhanced radiation have been studied through various methods. It was found that the most effective agent for irradiation-crosslinking was triallyl isocyanurate (TAIC) among four kinds of polyfunctional monomers. Gel content (65.6%) was formed for EVOH-44 (content of ethylene is 44 mol%) at 200 kGy with 5% TAIC, but for EVOH-32 (content of ethylene is 32 mol%), only 37.4% gel content was formed under the same conditions. This result showed that the more the content of ethylene units comprised in EVOH, the easier the chemical bonds could be formed between different molecular chains. Tensile strength and elastic modulus increased after crosslinking at high test temperature and elongation at break decreased at the same time. Hygroscopicity of EVOH showed noticeable decrease after enhancement radiation-crosslinking.

  13. Preparation of lignosulfonate-acrylamide-chitosan ternary graft copolymer and its flocculation performance.

    Science.gov (United States)

    He, Kunpeng; Lou, Tao; Wang, Xuejun; Zhao, Wenhua

    2015-11-01

    As flocculant plays an important role in wastewater treatment, searching for high efficient and cost-effective flocculants has always become the challenge in chemical industry. In the current work, lignosulfonate-acrylamide-chitosan ternary copolymer was designed and prepared as a new kind of flocculant. The elemental analysis and structure characterization of FTIR and XRD showed that acrylamide successfully grafted onto the two natural polymers and amorphous macromolecules were formed. The natural polymers-based flocculant was water soluble and pH independent. As it had multiple functional groups from the raw materials, the amphoteric flocculant showed high color removal efficiency to anionic (acid blue 113, >95%), neutral (reactive black 5, >95%) and cationic dyes (methyl orange, >50%) in a wide range of flocculant dosage and pH windows. The ternary flocculant, based on lignosulfonate, chitosan, and acrylamide, might be a promising material in practical applications from the perspective of cost, source and performance.

  14. Preparation and Biological Properties of Platinum(II Complex-Loaded Copolymer PLA-TPGS

    Directory of Open Access Journals (Sweden)

    Ha Phuong Thu

    2013-01-01

    Full Text Available A new nanodrug system containing bis(menthone thiosemicarbazonato Platinum(II complex (Pt-thiomen encapsulated with the block copolymers polylactide-d-α-tocopheryl polyethylene glycol 1000 succinate (PLA-TPGS was prepared by a modified solvent extraction/evaporation technique. The characteristics of the nanoparticles including surface morphology, size distribution, structure, and biological activities such as antimicrobial and cytotoxic activities were in vitro investigated. The spherical nanoparticles were around 50 nm in size with core-shell structure and narrow-size distribution. The encapsulated Pt-thiomen can avoid interaction with proteins in the blood plasma. The inhibitory activity of Pt-thiomen-loaded PLA-TPGS nanoparticles on the growth of some bacteria, fungi, and Hep-G2 cells suggests a possibility of developing PLA-TPGS-Pt-thiomen nanoparticles as one of the potential chemotherapeutic agents.

  15. Anti-fouling ultrafiltration membrane prepared from polysulfone-graft-methyl acrylate copolymers by UV-induced grafting method.

    Science.gov (United States)

    Hua, Helin; Li, Na; Wu, Linlin; Zhong, Hui; Wu, Guangxial; Yuan, Zonghuan; Lin, Xiangwei; Tang, Lianyi

    2008-01-01

    Membrane fouling is one of the most important challenges faced in membrane ultrafiltration operations. The copolymers of polysulfone-graft-methyl acrylate were synthesized by homogeneous photo-initiated graft copolymerization. The variables affecting the degree of grafting, such as the time of UV (Ultraviolet-visible) irradiation and the concentrations of the methyl acrylate and photoinitiator, were investigated. The graft copolymer membranes were prepared by the phase inversion method. The chemical and morphological changes were characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR/FT-IR), scanning electron microscopy, and water contact angles measurements. Results revealed that methyl acrylate groups were present on the membranes and the graft degree of methyl acrylate had remarkable effect on the performance of membranes. Pure water contact angle on the membrane surface decreases with the increase of methyl acrylate graft degree, which indicated that the hydrophilicity of graft copolymer membranes was improved. The permeation fluxes of pure water and bovine serum albumin solution were measured to evaluate the antifouling property of graft copolymer membranes, the results of which have shown an enhancement of antifouling property for graft copolymer membranes.

  16. Matrix-assisted laser desorption/ionization sample preparation optimization for structural characterization of poly(styrene-co-pentafluorostyrene) copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Tisdale, Evgenia; Kennedy, Devin; Wilkins, Charles, E-mail: cwilkins@uark.edu

    2014-01-15

    Graphical abstract: -- Highlights: •We optimized sample preparation for MALDI TOF poly(styrene-copentafluorostyrene) co-polymers. •Influence of matrix choice was investigated. •Influence of matrix/analyte ratio was examined. •Influence of analyte/salt ratio (for Ag+ salt) was studied. -- Abstract: The influence of the sample preparation parameters (the choice of the matrix, matrix:analyte ratio, salt:analyte ratio) was investigated and optimal conditions were established for the MALDI time-of-flight mass spectrometry analysis of the poly(styrene-co-pentafluorostyrene) copolymers. These were synthesized by atom transfer radical polymerization. Use of 2,5-dihydroxybenzoic acid as matrix resulted in spectra with consistently high ion yields for all matrix:analyte:salt ratios tested. The optimized MALDI procedure was successfully applied to the characterization of three copolymers obtained by varying the conditions of polymerization reaction. It was possible to establish the nature of the end groups, calculate molecular weight distributions, and determine the individual length distributions for styrene and pentafluorostyrene monomers, contained in the resulting copolymers. Based on the data obtained, it was concluded that individual styrene chain length distributions are more sensitive to the change in the composition of the catalyst (the addition of small amount of CuBr{sub 2}) than is the pentafluorostyrene component distribution.

  17. Allergenic proteins of natural rubber latex.

    Science.gov (United States)

    Yeang, H Y; Arif, Siti Arija M; Yusof, Faridah; Sunderasan, E

    2002-05-01

    As the living cytoplasm of laticiferous cells, Hevea brasiliensis latex is a rich blend of organic substances that include a mélange of proteins. A small number of these proteins have given rise to the problem of latex allergy. The salient characteristics of H. brasiliensis latex allergens that are recognized by the International Union of Immunological Societies (IUIS) are reviewed. These are the proteins associated with the rubber particles, the cytosolic C-serum proteins and the B-serum proteins that originate mainly from the lutoids. Procedures for the isolation and purification of latex allergens are discussed, from latex collection in the field to various preparative approaches adopted in the laboratory. As interest in recombinant latex allergens increases, there is a need to validate recombinant proteins to ascertain equivalence with their native counterparts when used in immunological studies, diagnostics, and immunotherapy.

  18. Thermosensitive Polymer Nanocontainers Prepared by Self-Assembly of Block Copolymers

    Institute of Scientific and Technical Information of China (English)

    Chen Xiangrong; Ding Xiaobing; Zheng Zhaohui; Peng Yuxing

    2004-01-01

    In recent years, considerable effort has been devoted to the preparation of polymer nanocontainers because of their unique advantages. Compared to polymer microspheres or micelles,polymer nanocontainers are hollow-sphere structures and can encapsulate large quantities of guest molecules or large-sized guests within the "empty" core domain. Compared to polymer vesicles,polymer nanocontainers have enough mechanical stability to prevent them from structure changes due to covalent or ionic interactions responsible for their formation. Therefore, polymer nanocontainers have many potential applications such as confined reaction vesicles, drug carriers,protective shells for cells or enzymes, artificial cells and so on. However, most of polymer nanocontainers reported by now, load and release guest molecules from their interior only through diffuse mechanism. It is rather difficult to control intelligently the process based on demands. In order to solve this problem, one promising strategy is to design intelligent polymer nanocontainers.They can undergo reversible structural transitions from a closed to an open state with the help of external stimuli.In this paper, we report on our preliminary study of the thermosensitive polymer nanocontainers formed by self-assembly of the block copolymers PCEMA-b-PNIPAM and sequent photo-crosslinking of PCEMA shells.Block copolymers PCEMA-b-PNIPAM were prepared by reacting PHEMA-b-PNIPAM with excess cinnamoyl chloride in pyridine at room temperature, where PHEMA-b-PNIPAM was prepared by reacting succinimidyl ester of PHEMA-COOH with PNIPAAm-NH2, similar to the method of the literature. The block copolymers were characterized by FTIR and 1H-NMR and GPC.To obtain polymer vesicles, deionized water, as a precipitant, was added at a rate of 0.3wt%/10s with vigorous stirring to the PCEMA-b-PNIPAM solution in THE After the formation of polymer vesicles, more water was added until the water content reached ca.50wt%. The hollow structure of the

  19. LaTeX for Agricultural Extension Professionals

    Science.gov (United States)

    LaTeX is a free open source document preparation system for professional quality documents and presentation materials. Extension professionals, trying to reach their audience though various forms of printed and online resources, can benefit from the vast potential of LaTeX. Using LaTeX empowers the ...

  20. Preparation of core-crosslinked linear-dendritic copolymer micelles with enhanced stability and their application for drug solubilisation.

    Science.gov (United States)

    Zhou, Zhengyuan; Forbes, Robert T; D'Emanuele, Antony

    2017-05-15

    In this study we explore the preparation of core-crosslinked micelles of linear-dendritic methoxy-poly(ethylene glycol) (MPEG)-co-poly(ester-sulfide) (PES) polymers to improve the stability of such polymeric micelle systems against premature disintegration and drug release. A series of MPEG-PES copolymers were synthesised via stepwise reactions of acetylation and thiol-ene photoreaction. Surface tension measurement showed that the copolymers with ethenyl surface groups could self-associate in dilute aqueous solutions to form micelles. Crosslinking within the micelle cores in the presence of dithioerythritol (DTT) linker was initiated under UV radiation. The formation of core-crosslinked micelles was confirmed by HPLC in combination with charged aerosol detection (CAD). The copolymers were found to readily hydrolyse under acidic conditions due to the ester-containing dendrons. Drug solubilisation capacities of the micellar solutions were determined using griseofulvin as a poorly water-soluble model drug. The solubility of griseofulvin showed a 10-fold enhancement in 1% w/v micelle solution and increased with the concentration of the copolymers. Drug release studies indicated that a more sustained release of griseofulvin was achieved for the core-crosslinked micelles compared to the non-crosslinked micelles, attributable to greater stability of the crosslinked core structure. The findings of this study present a new pathway towards developing biodegradable polymeric nanocarriers. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Removal of heavy metal ions from wastewater by a novel HEA/AMPS copolymer hydrogel: preparation, characterization, and mechanism.

    Science.gov (United States)

    Li, Zhengkui; Wang, Yueming; Wu, Ningmei; Chen, Qichun; Wu, Kai

    2013-03-01

    This study aims to synthesize 2-hydroxyethyl acrylate (HEA) and 2-acrylamido-2-methylpropane sulfonic (AMPS) acid-based hydrogels by gamma radiation and to investigate their swelling behavior and heavy metal ion adsorption capabilities. The copolymer hydrogels prepared were characterized via scanning electron microscopy, Fourier transformed infrared spectra, thermal gravimetric analysis, and X-ray photoelectron spectroscopy. The research showed that the copolymer hydrogel was beneficial for permeation due to its porous structure. In addition, the experimental group A-2-d [70 % water volume ratio and (n (AMPS)/n (HEA)) =1:1] was an optimal adsorbent. The optimal pH was 6.0 and the optimal temperature was 15 °C. Pb(2+), Cd(2+), Cu(2+), and Fe(3)+ achieved adsorption equilibriums within 24 h, whereas Cr(3+) reached equilibrium in 5 h. Pb(2)+, Cd(2+), Cr(3+), and Fe(3+) maximum load capacity was 1,000 mg L(-1), whereas the Cu(2+) maximum capacity was 500 mg L(-1). The priority order in the multicomponent adsorption was Cr(3+)>Fe(3+)>Cu(2+)>Cd(2+)>Pb(2+). The adsorption process of the HEA/AMPS copolymer hydrogel for the heavy metal ions was mainly due to chemisorption, and was only partly due to physisorption, according to the pseudo-second-order equation and Langmuir adsorption isotherm analyses. The HEA/AMPS copolymer hydrogel was confirmed to be an effective adsorbent for heavy metal ion adsorption.

  2. Preparation of starch-poly-glutamic acid graft copolymers by microwave irradiation and the characterization of their properties.

    Science.gov (United States)

    Xu, Jingyuan; Krietemeyer, Elizabeth F; Finkenstadt, Victoria L; Solaiman, Daniel; Ashby, Richard D; Garcia, Rafael A

    2016-04-20

    Graft copolymers of waxy maize starch and poly-γ-glutamic acid (PGA) were produced in an aqueous solution using microwave irradiation. The microwave reaction conditions were optimized with regard to temperature and pH. The temperature of 180°C and pH7.0 were the best reaction conditions resulting in a PGA graft of 0.45% based on nitrogen analysis. The average graft content and graft efficiency for the starch-PGA graft copolymer prepared at 180°C and pH7.0 were 4.20% and 2.73%, respectively. The starch-PGA graft copolymer produced at 180°C and pH7.0 could absorb more than 20 times its own weight amount of water and form a gel. The preliminary rheology study revealed that the starch-PGA graft copolymer gel exhibited viscoelastic solid behavior while the control sample of waxy starch showed viscoelastic liquid behavior. Published by Elsevier Ltd.

  3. Anti-fouling ultrafiltration membrane prepared from polysulfone-graft-methyl acrylate copolymers by UV-induced grafting method

    Institute of Scientific and Technical Information of China (English)

    HUA Helin; LI Na; WU Linlin; ZHONG Hui; WU Guangxia; YUAN Zonghuan; LIN Xiangwei; TANG Lianyi

    2008-01-01

    Membrane fouling is one of the most important challenges faced in membrane ultrafiltration operations. The copolymers of polysulfone-graft-methyl acrylate were synthesized by homogeneous photo-initiated graft copolymerization. The variables affecting the degree of grafting, such as the time of UV(Ultraviolet-visible)irradiation and the concentrations of the methyl acrylate and photoinitiator, were investigated. The graft copolymer membranes were prepared by the phase inversion method. The chemical and morphological changes were characterized by attenuated total reflection-Fourier transform infrared spectroscopy(ATR/FT-IR), scanning electron microscopy, and water contact angles measurements. Results revealed that methyl acrylate groups were present on the membranes and the graft degree of methyl acrylate had remarkable effect on the performance of membranes. Pure water contact allgle on the membrane surface decreases with the increase of methyl acrylate graftdegree. which indicated that the hydrophilicity of graft copolymer membranes Was improved. The permeation fluxes of pure water and bovine serum albumin solution were measured to evaluate the antifouling property of graft copolymer membranes, the results of which have shown an enhancement of antifouling property for graft copoly mermembranes.

  4. Synthesis, structure and properties of new tung oil-styrene-divinylbenzene copolymers prepared by thermal polymerization.

    Science.gov (United States)

    Li, Fengkui; Larock, Richard C

    2003-01-01

    A variety of new polymers ranging from rubbery materials to tough and rigid plastics have been prepared by the thermal copolymerization of tung oil, styrene, and divinylbenzene. The thermal copolymerization is performed in the temperature range of 85-160 degrees C with variations in the stoichiometry, oxygen uptake, peroxides, and metallic catalysts used. Gelation of the reactants typically occurs at temperatures higher than 140 degrees C, and fully cured thermosets are obtained after post-curing at 160 degrees C. The fully cured thermosets are determined by Soxhlet extraction to contain approximately 90-100% cross-linked materials, and (1)H NMR and FTIR spectroscopy indicates that the cross-linked materials are random copolymers. The new bulk polymeric materials obtained are light yellow and transparent with glossy surfaces, and possess glass transition temperatures of -2 to +116 degrees C, cross-link densities of 1.0 x 10(3)-2.5 x 10(4) mol/m(3), coefficients of linear thermal expansion of 2.3 x 10(-4)-4.4 x 10(-4) per degrees C, compressive moduli of 0.02-1.12 GPa, and compressive strengths of 8-144 MPa. These materials are thermally stable below 300 degrees C and exhibit a major thermal degradation with a maximum degradation rate at 493-506 degrees C.

  5. An Injectable Hydrogel Prepared Using a PEG/Vitamin E Copolymer Facilitating Aqueous-Driven Gelation.

    Science.gov (United States)

    Zhang, Jianfeng; Muirhead, Ben; Dodd, Megan; Liu, Lina; Xu, Fei; Mangiacotte, Nicole; Hoare, Todd; Sheardown, Heather

    2016-11-14

    Hydrogels have been widely explored for biomedical applications, with injectable hydrogels being of particular interest for their ability to precisely deliver drugs and cells to targets. Although these hydrogels have demonstrated satisfactory properties in many cases, challenges still remain for commercialization. In this paper, we describe a simple injectable hydrogel based on poly(ethylene glycol) (PEG) and a vitamin E (Ve) methacrylate copolymer prepared via simple free radical polymerization and delivered in a solution of low molecular weight PEG and Ve as the solvent instead of water. The hydrogel formed immediately in an aqueous environment with a controllable gelation time. The driving force for gelation is attributed to the self-assembly of hydrophobic Ve residues upon exposure to water to form a physically cross-linked polymer network via polymer chain rearrangement and subsequent phase separation, a spontaneous process with water uptake. The hydrogels can be customized to give the desired water content, mechanical strength, and drug release kinetics simply by formulating the PEGMA-co-Ve polymer with an appropriate solvent mixture or by varying the molecular weight of the polymer. The hydrogels exhibited no significant cytotoxicity in vitro using fibroblasts and good tissue compatibility in the eye and when injected subcutaneously. These polymers thus have the potential to be used in a variety of applications where injection of a drug or cell containing depot would be desirable.

  6. Biocompatible branched copolymer nanoparticles prepared by RAFT polymerization as MRI/PET bimodal tracers

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Chang-Tong [Lee Kong Chian School of Medicine, Nanyang Technological University (Singapore); Tao, He; Jackson, Alexander W [Institute of Chemical and Engineering Sciences, Agency for Science Technology and Research (Singapore); Chandrasekharan, Prashant [Laboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (Singapore); Padmanabhan, Parasuraman [Lee Kong Chian School of Medicine, Nanyang Technological University (Singapore); Gulyás, Balázs; Halldin, Christer [Lee Kong Chian School of Medicine, Nanyang Technological University (Singapore); Karolinska Institutet, Department of Clinical Neuroscience, Stockholm (Sweden)

    2015-05-18

    Stable branched copolymer nanoparticles of varying size (Dh = 20 – 35 nm) have been developed and employed as MRI nano-sized contrast agents. RAFT polymerization has been employed to prepare these novel nanoparticles possessing DO3A macrocycles within their cores and succinimidyl ester benzoate functionalities within their coronas. It has been demonstrated that these nanoparticles can chelate gadolinium and in vitro cytotoxicity studies using HK-2 cells established their negligible toxicity profile. In vivo MRI experiments showed that these nanoparticles have a high relaxivity and a long blood retention time. Xenograft experiments further illustrated the ability of these nanoparticles to perfuse and passively accumulate in tumor cells, presumably through the enhanced EPR effect. The presence of the succinimidyl ester benzoate functionalities within the nanoparticle coronas will permit future surface modification with fluorophores or targeting moieties to generate nanoparticles to study opportunities for bimodal imaging nano-probes or active cell targeting contrast agents. The chelation with PET radioisotopes (68Ga(III) or 64Cu(II)) can afford various PET tracers.

  7. Conformational Study of Polypeptide Chains Grafted on the Surface of Polylactide Latex Particle

    Directory of Open Access Journals (Sweden)

    Satoshi Tanimoto

    2009-01-01

    Full Text Available Polylactide (PLA latex particle covered with polypeptide chains were prepared by means of solvent exchange method from PLA and PLA-block-polypeptide block copolymer solutions. PLA segment of the block copolymer and PLA homopolymer formed a core of the particle, and the polypeptide segment of the block copolymer, which is designed as tightly fixed biodegradable emulsifier, formed corona around the particle surface. This picture was supported by the fact that zeta-potential of PLA latex particle covered with polypeptide segment was different from that of bare PLA particle because of the presence of the ionizable group in the polypeptide chains. To clarify the effect of the ionizable group on conformation of the polypeptide chain, the relation between the polypeptide chain length and the area occupied by the single block chain was evaluated. The result that the occupied area per a polypeptide chain was linearly increased with the increase in the polypeptide chain length indicates that the polypeptide chains trail on the particle surface and did not take helical structures.

  8. RANDOM COPOLYMER OF PROPYLENE OXIDE AND ETHYLENE OXIDE PREPARED BY DOUBLE METAL CYANIDE COMPLEX CATALYST

    Institute of Scientific and Technical Information of China (English)

    Yi-jun Huang; Guo-rong Qi; Guan-xi Chen

    2002-01-01

    Copolymerization of propylene oxide (PO) and ethylene oxide (EO) using double metal cyanide (DMC) complex as the catalyst was carried out. The structure of random copolymers was confirmed by 13C-NMR and IR spectra. 1H-NMR analysis shows that the EO content in the copolymer is the same as that in the initial monomer feed. Moderate molecular weight copolymers with various EO content were obtained and their values of molecular weight distribution (MWD) fell in the range of 1.21-1.55. It was found that the molecular weight of copolymers is controlled by the mass ratio ofEO + PO to initiator moles used. The reaction rate as well as polymer yield decrease with increasing EO content in the feed composition.

  9. Conjugated Polymer Chains Confined in Vertical Nanocylinders of a Block-Copolymer Film: Preparation, Characterization, and Optoelectronic Function

    KAUST Repository

    Dong, Ban Xuan

    2013-01-15

    Hybrid materials composed of phase-separated block copolymer films and conjugated polymers of the phenylenevinylene family (PPV) are prepared. The PPV chains are embedded in vertical cylinders of nanometer diameter in the block-copolymer films. The cylinders span continuously the whole film thickness of 70 nm. Incorporation of the PPV chains into the one-dimensional cylinders leads to modified photoluminescence spectra and to large absorption anisotropy. The hybrid films show electroluminescence from the PPV chains in a simple light-emitting device at minute doping concentrations, and also exhibit a factor of 19 increase in electron transport efficiency along the single PPV chains. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Preparation and characterization of porous DVB copolymers and their applicability for adsorption (solid-phase extraction) of phenol compounds

    Science.gov (United States)

    Sobiesiak, Magdalena; Podkoscielna, Beata

    2010-12-01

    Using DVB, three new porous copolymers in the form of microspheres were prepared, characterized and used as adsorbents for phenol and its chlorinated derivatives. As the monomers: 4,4'-bis(maleimidodiphenyl)methane (BM), 2,3-bis(2-hydroxy-3-methylacryloyloxy-propoxy)naphthalene (2,3-NAF) and 2,3-epoxypropyl methacrylate (GLY) were used. All the studied materials were synthesized under the same conditions by means of suspension copolymerization. The DVB copolymers were characterized by elemental analysis, FTIR spectroscopy, TG and DSC analyses and N 2 sorption. The off-line solid-phase extraction method (SPE) was used to estimate sorption properties of the copolymers. The results show that the newly obtained materials are mesoporous but their shape of pores and chemical structures are different. BM-DVB and GLY-DVB are characterized by slit-shaped pores and wide pore size distribution. 2,3-NAF-DVB also possesses slit pores but distribution of pore size is narrower. Of those studied BM-DVB is the most interesting material. It has good sorption properties and heat resistance.

  11. Preparation of transition metal nanoparticles and surfaces modified with (co)polymers synthesized by RAFT

    Science.gov (United States)

    McCormick, III, Charles L.; Lowe, Andrew B.; Sumerlin, Brent S.

    2011-12-27

    A new, facile, general one-phase method of generating thiol-functionalized transition metal nanoparticles and surfaces modified by (co)polymers synthesized by the RAFT method is described. The method includes the steps of forming a (co)polymer in aqueous solution using the RAFT methodology, forming a colloidal transition metal precursor solution from an appropriate transition metal; adding the metal precursor solution or surface to the (co)polymer solution, adding a reducing agent into the solution to reduce the metal colloid in situ to produce the stabilized nanoparticles or surface, and isolating the stabilized nanoparticles or surface in a manner such that aggregation is minimized. The functionalized surfaces generated using these methods can further undergo planar surface modifications, such as functionalization with a variety of different chemical groups, expanding their utility and application.

  12. Lignin-derived thermoplastic co-polymers and methods of preparation

    Science.gov (United States)

    Naskar, Amit K.; Saito, Tomonori; Pickel, Joseph M.; Baker, Frederick S.; Eberle, Claude Clifford; Norris, Robert E.; Mielenz, Jonathan Richard

    2014-06-10

    The present invention relates to a crosslinked lignin comprising a lignin structure having methylene or ethylene linking groups therein crosslinking between phenyl ring carbon atoms, wherein said crosslinked lignin is crosslinked to an extent that it has a number-average molecular weight of at least 10,000 g/mol, is melt-processible, and has either a glass transition temperature of at least 100.degree. C., or is substantially soluble in a polar organic solvent or aqueous alkaline solution. Thermoplastic copolymers containing the crosslinked lignin are also described. Methods for producing the crosslinked lignin and thermoplastic copolymers are also described.

  13. Neonatal sensitization to latex.

    Science.gov (United States)

    Worth, J

    2000-05-01

    Babies born in delivery rooms of hospitals are exposed to latex through skin and mucous membrane contact with prepowdered latex gloves worn by midwives and doctors, and through the inhalation of latex-bound starch powder in the air of the delivery room. This paper examines the hypothesis that they are at risk for latex sensitization, and that part of the sharp increase of childhood asthma, eczema and anaphylaxis in the past 30-40 years may be linked. These possibilities seem hitherto unsuspected. In over 700 papers on latex allergy no mention of neonatal exposure to latex has been found. Even obstetric papers discussing the risks for an atopic mother (atopy - a tendency to develop allergies) do not seem to anticipate any risk for the baby, who might also be atopic. Latex allergy is primarily regarded as an occupational hazard. This paper suggests that it is a hazard for every baby handled by latex gloves at birth. Copyright 2000 Harcourt Publishers Ltd.

  14. Block copolymers of poly(L-lactide) and poly(ε-caprolactone) or poly(ethylene glycol) prepared by reactive extrusion

    NARCIS (Netherlands)

    Stevels, W.M.; Bernard, A.; Witte, van de P.; Dijkstra, P.J.; Feijen, J.

    1996-01-01

    Blends of poly(L-lactide) (PLLA) and poly(-caprolactone) (PCL) were prepared in a co-rotating twin screw miniextruder (40 rpm, 200°). It was attempted to prepare multiblock copolymers by allowing a controlled number of transesterification reactions. Various cat-alysts (n-Bu3SnOMe, Sn(Oct)2, Ti(OBu)4

  15. Block copolymers of poly(l-lactide) and poly(e-caprolactone) or poly(ethylene glycol) prepared by reactive extrusion

    NARCIS (Netherlands)

    Stevels, W.M.; Bernard, A.; van de Witte, P.; van de Witte, P.; Dijkstra, Pieter J.; Feijen, Jan

    1996-01-01

    Blends of poly(L-lactide) (PLLA) and poly(-caprolactone) (PCL) were prepared in a co-rotating twin screw miniextruder (40 rpm, 200°). It was attempted to prepare multiblock copolymers by allowing a controlled number of transesterification reactions. Various cat-alysts (n-Bu3SnOMe, Sn(Oct)2,

  16. LATEX for Librarians.

    Science.gov (United States)

    Boatright, George S.

    This paper presents the basics of "LATEX," a computerized typesetting program popular with mathematicians and other writers of technical papers, and compares it to conventional word processing programs. LATEX, which requires a text editor such as WordPad or NotePad--the text editor is used to produce and input file which the LATEX program…

  17. The Morphology of Emulsion Polymerized Latex Particles

    Science.gov (United States)

    Wignall, G. D.; Ramakrishnan, V. R.; Linne, M. A.; Klein, A.; Sperling, L. H.; Wai, M. P.; Gelman, R. A.; Fatica, M. G.; Hoerl, R. H.; Fisher, L. W.

    1987-11-01

    Under monomer starved feed conditions, emulsion polymerization of perdeuterated methyl methacrylate and styrene in the presence of preformed polymethylmethacrylate latexes resulted in particles with a core-shell morphology, as determined by small-angle neutron scattering (SANS) analysis for a hollow sphere. The locus of polymerization of the added deuterated monomer is therefore at the particle surface. In similar measurements a statistical copolymer of styrene and methyl methacrylate was used as seed particles for further polymerization of trideuteromethyl methacrylate. The resulting polymer latex was again shown to have a core-shell morphological structure as determined by SANS. SANS experiments were also undertaken on polystyrene latexes polymerized by equilibrium swelling methods, with deuterated polymer forming the first or second step. The experiments covered a molecular weight range of 6 x 10{sup 4} 10{sup 6} the molecular weights are consistent with the experimental errors, indicating that the deuterium labeled molecules are randomly distributed in the latex. These results led to the finding that the polymer chains were constrained in the latex particles by factors of 2 to 4 from the relaxed coil dimensions. For M < 10{sup 6} g/mol SANS gave zero angle scattering intensities much higher than expected on the basis of a random distribution of labeled molecules. Several models were examined, including the possible development of core-shell structures at lower molecular weights.

  18. PLA-PEG-PLA copolymer-based polymersomes as nanocarriers for delivery of hydrophilic and hydrophobic drugs: preparation and evaluation with atorvastatin and lisinopril.

    Science.gov (United States)

    Danafar, H; Rostamizadeh, K; Davaran, S; Hamidi, M

    2014-10-01

    Tri-block poly(lactide)-poly(ethylene glycol)-poly(lactide) (PLA-PEG-PLA) copolymers were synthesized and used to prepare polymersomes loaded separately by the hydrophobic and hydrophilic model drugs, atorvastatin and lisinopril, respectively. The resulting nanostructures were characterized by various techniques such as FTIR, DSC, PCS and AFM. The polymersomes exhibited high encapsulation efficiencies of almost 78% and 70.8% for atorvastatin and lisinopril, respectively. Investigation on FTIR and DSC results revealed that such a high encapsulation efficiency is due to strong interaction between atorvastatin and the copolymer. The impact of drug/copolymer ratio and copolymer composition on drug-loading efficiency and drug release behavior were also studied. The results showed that in case of lisinopril, polymersomes exhibited a triphasic drug release, while for atorvastatin a biphasic release profile was obtained. Overall, the results indicated that PLA-PEG-PLA polymersomes can be considered as a promising carrier for both hydrophilic and hydrophobic drugs.

  19. The preparation of composite microsphere with hollow core/porous shell structure by self-assembling of latex particles at emulsion droplet interface.

    Science.gov (United States)

    He, Xiao Dong; Ge, Xue Wu; Wang, Mo Zhen; Zhang, Zhi Cheng

    2006-07-15

    A submicrometer-scaled polystyrene/melamine-formaldehyde hollow microsphere composite was prepared by self-assembling of sulfonated polystyrene (SPS) latex particles at the interface of emulsion droplets and then being fixed in place using a hard melamine-formaldehyde (MF) composite layer. For control-released purposes, the influential factors that control the size and uniformity of the packed-droplets and the permeability of the composite shell, including the initial particle location, the hydrophilicity and the size of colloidal templates, the oil phase solvent and reserving time of emulsions after the addition of MF prepolymer, were further studied. Relatively uniform sized particle packed-droplets with an average diameter of 10 microm were obtained. The assembled SPS particles kept ordering and minimal conglutination after the preparation of composite microspheres, which allows of controlling the permeability from the interstices between the particles. Porous-mesh-structured MF composite layer was formed to further control the permeability. The morphology of emulsions and composite microspheres were characterized by optical microscopy, scanning and transmission electron microscopy.

  20. Preparation of shell cross-linked nano-objects from hybrid-peptide block copolymers.

    Science.gov (United States)

    Rodríguez-Hernández, Juan; Babin, Jérôme; Zappone, Bruno; Lecommandoux, Sébastien

    2005-01-01

    Supramolecular structures formed by self-assembly of diblock copolymers in solution are stable over restricted environmental conditions: concentration, temperature, pH, or ion strength among others. To enlarge their domain of application, it appears necessary to develop stabilization strategies. We report here different strategies to stabilize the shell of micelles formed by self-assembly of amphiphilic polydiene-b-polypeptide diblock copolymers. For this purpose, covalent bonds can be formed between either amine or carboxylic acid groups distributed along the soluble peptide block and a cross-linking agent that contains respectively aldehyde or amine functions. Shell stabilization affords systems with unique properties that combine three main advantages: shape persistence, control of the porosity, and stimuli-responsive behavior. The covalent capture of such macromolecular objects has been studied by light scattering, AFM, and conductimetry measurements.

  1. Controllable preparation of polystyrene-methylacrylic acid latex templates and silica hollow spheres%聚苯乙烯-甲基丙烯酸模板与SiO2空心微球可控性制备

    Institute of Scientific and Technical Information of China (English)

    石莉萍; 刘纯

    2012-01-01

    利用无皂聚合和乳液聚合,制备了聚苯乙烯-甲基丙烯酸胶体模板.聚苯乙烯-甲基丙烯酸胶体模板粒径分别控制为363,349,160和56 nm,实现了模板粒径的可控制备.利用制备的聚苯乙烯-甲基丙烯酸系列胶体模板,以偏硅酸钠为前驱体,煅烧去除模板后,制备了不同粒径及壁厚的二氧化硅空心微球.所制备的样品粒径在69~ 405 nm之间,壁厚在11 ~27 nm之间变化.利用扫描电子显微镜、透射电子显微镜和傅立叶变换红外光谱仪,对乳液模板、核壳复合材料及二氧化硅空心球形貌进行了表征,提出了聚苯乙烯-甲基丙烯酸模板与二氧化硅空心微球粒径调控的有效方法.%The polystyrene-methacrylic acid latex templates were prepared by emulsifier-free and emulsifier emulsion polymerization. The average diameters of the polystyrene-methacrylic acid latex templates were respectively controlled at 363 , 349 , 160 and 56 nm to realize controllable preparation of polystyrene-methylacrylic acid latex templates. Whereafter, the hollow silica microspheres with various grain size and shell thickness were prepared after calcination to remove the templates with polystyrene-methy lacrylic acid latexes as templates and sodium silicate as precursor. The diameters of the silica hollow microspheres range from 69 to 405 nm with the shell thicknesses from 11 to 27 nm. The latex templates, core-shell composites and silica hollow spheres were characterized by scanning electron microscopy ( SEM ) , transmission electron microscopy ( TEM ) and FT-infrared spectroscopy ( FT-IR ) . An effective method for controllable preparation of polystyrene-methylacrylic acid latex templates and silica hollow spheres was proposed.

  2. Preparation of amphiphilic block copolymer containing triazene moieties and fluorescence study

    Indian Academy of Sciences (India)

    Emil C Buruiana; Andreea L Chibac; Violeta Melinte; Tinca Buruiana

    2013-01-01

    The present study describes the synthesis via microwave accelerated reversible additionfragmentation chain transfer (RAFT) polymerization of an amphiphilic block copolymer poly(acrylic acid)-b-poly(dodecylacrylamide-co-1-(phenyl)-3-(2-methacryloyloxyethyl carbamoyloxyethyl)-3-methyltriazene-1) [PAA-b-(PDA-co-PUMA-T)]. The structure and the chemical composition of the block copolymer were confirmed by spectral/thermal analysis. The photoreactivity of the triazene sequences from PAA-b-(PDA-co-PUMA-T) was quantified by UV/vis irradiation in chloroform/dimethylformamide solutions and in thin film, indicating that the solvent polarity modifies with an order of magnitude the rate constant values. The lower rate constant in film state (film = 1.3 × 10−3 s-1), shows that the higher mobility of polymeric chains in solution allow a more rapid orientation, favourable to the triazene bond cleavage. The capability of block copolymer to form micelles in aqueous environment and implicitly, its critical micelle concentration (CMC) was evidenced through fluorescence measurements using pyrene probe (10-6 M), the CMC value being of 4.64 × 10−3 g L-1 PAA--(PDA--PUMA-T) (3.27 × 10−7 M). Experiments of fluorescence quenching with various metal cations (UO$^{2+}_{2}$, Fe2+, Fe3+, Ni2+, Cu2+, Co2+, Pb2+ and Hg2+) suggested that such a block copolymer could find applications as fluorescence-based chemosensor for the detection of iron cations in homogeneous organic solutions or aqueous environments by thin films.

  3. Advanced analytical methods for the structure elucidation of polystyrene-b-poly(n-butyl acrylate) block copolymers prepared by reverse iodine transfer polymerisation

    Energy Technology Data Exchange (ETDEWEB)

    Wright, Trevor Gavin; Pfukwa, Helen; Pasch, Harald, E-mail: hpasch@sun.ac.za

    2015-09-10

    Reverse iodine transfer polymerisation (RITP) is a living radical polymerisation technique that has shown to be feasible in synthesising segmented styrene-acrylate copolymers. Polymers synthesised via RITP are typically only described regarding their bulk properties using nuclear magnetic resonance spectroscopy and size exclusion chromatography. To fully understand the complex composition of the polymerisation products and the RITP reaction mechanism, however, it is necessary to use a combination of advanced analytical methods. In the present RITP procedure, polystyrene was synthesised first and then used as a macroinitiator to synthesise polystyrene-block-poly(n-butyl acrylate) (PS-b-PBA) block copolymers. For the first time, these PS-b-PBA block copolymers were analysed by a combination of SEC, in situ{sup 1}H NMR and HPLC. {sup 1}H NMR was used to determine the copolymer composition and the end group functionality of the samples, while SEC and HPLC were used to confirm the formation of block copolymers. Detailed information on the living character of the RITP process was obtained. - Highlights: • Comprehensive analysis of novel block copolymers. • Polymers were prepared for the first time by reverse iodine transfer polymerisation. • Combination of SEC, NMR, kinetic NMR, HPLC and comprehensive 2D-HPLC was used. • Detailed information about complex molecular composition and polymerisation kinetics was obtained.

  4. 建筑保温隔热弹性乳胶漆的研制%Preparation of Architectural Thermal Insulation Flexible Latex Paint

    Institute of Scientific and Technical Information of China (English)

    王谷峰; 王凯; 柏金成

    2011-01-01

    The thermal insulation flexible latex paint is mating material of exterior wall in external insulation system. The raw material, basic formula, preparation technology and the construction method of this elastic paint were introduced. Its main extender is industrial waste coal flying ash cenosphere substitute the expensive hollow glass beads. This elastic paint has low dry density and high efficient in thermal insulation property. It plays an important role in covering the protector layer crack, preventing the decoration paint film split, enhancing thermal insulation and improving energy efficiency.%保温隔热弹性乳胶漆是外墙外保温系统的配套材料,介绍了建筑外墙用保温隔热弹性乳胶漆的原材料、基本配方、制备工艺和施工方法,其功能性填料是用工业废渣粉煤灰漂珠代替价格昂贵的玻璃空心微珠,所研制的弹性乳胶漆干密度低、保温性能好,其漆膜能在遮蔽基层裂缝、防止装饰涂膜开裂、增强保温隔热效果、提高节能效率方面发挥重要作用。

  5. The preparation of an elastomer/silicate layer nanocompound with an exfoliated structure and a strong ionic interfacial interaction by utilizing an elastomer latex containing pyridine groups.

    Science.gov (United States)

    He, Shao-jian; Wang, Yi-qing; Feng, Yi-ping; Liu, Qing-sheng; Zhang, Li-qun

    2010-03-19

    A great variety of polymer/layered silicate (PLS) nanocomposites have been reported, however, there are few exfoliated PLS nanocomposites and their inorganic-organic interfaces are still a great problem, especially for the elastomers. In this research, a kind of exfoliated elastomer/silicate layer nanocompound was prepared and proved by XRD and TEM, in which 10 phr Na(+)-montmorillonite was dispersed in butadiene-styrene-vinyl pyridine rubber by latex compounding method with acidic flocculants. Moreover, a dynamic mechanical thermal analyzer (DMTA) suggested a strong interfacial interaction (interaction parameter B(H) = 4.91) between the silicate layers and macromolecules in addition to the weak inorganic-organic interfacial interaction, and solid state (15)N NMR indicated the formation of a strong ionic interface through the acidifying pyridine. Subsequently, a remarkable improvement of the dispersing morphology, mechanical performance and gas barrier property appeared, compared to that using calcium ion flocculants. This supports the formation of an exfoliated structure and an improved interfacial interaction.

  6. A simple method to prepare modified polyethersulfone membrane with improved hydrophilic surface by one-pot: The effect of hydrophobic segment length and molecular weight of copolymers.

    Science.gov (United States)

    Ran, Fen; Li, Jie; Lu, Yi; Wang, Lingren; Nie, Shengqiang; Song, Haiming; Zhao, Lei; Sun, Shudong; Zhao, Changsheng

    2014-04-01

    A simple method to prepare modified polyethersulfone (PES) membrane by one-pot is provided, and the method includes three steps: polymerization of vinyl pyrrolidone (VP), copolymerization of methyl methacrylate (MMA) and blending with PES. The effect of the PMMA segment length and molecular weight of the copolymer (PVP-b-PMMA-b-PVP, as an additive) on the structures and properties of the modified membranes was investigated. Activated partial thromboplastin time (APTT) tests indicated that with the increase of the poly(methyl methacrylate) (PMMA) segment length in the chains of the copolymers and with the increase of the molecular weight of the copolymers, the APTTs of the modified membranes increased to some extent, since less of the additives were lost during liquid-liquid phase separation process. Therefore, the copolymer was designed and prepared with appropriate ratio of poly(vinyl pyrrolidone) (PVP) to MMA and with appropriate molecular weight for better membrane performance. When the copolymer was blended in the membrane, the water permeance, protein anti-fouling property and sieving coefficients for PEG-12000 increased obviously. The simple, credible and feasible method had the potential to be used for the modification of membranes with improved blood compatibility, ultrafiltration and antifouling properties of biomaterials and for practical production.

  7. Rheological Properties of Hydrophobically Associative Copolymers Prepared in a Mixed Micellar Method Based on Methacryloxyethyl-dimethyl Cetyl Ammonium Chloride as Surfmer

    Directory of Open Access Journals (Sweden)

    Rui Liu

    2014-01-01

    Full Text Available A novel cationic surfmer, methacryloxyethyl-dimethyl cetyl ammonium chloride (DMDCC, is synthesized. The micellar properties, including critical micelle concentration and aggregation number, of DMDCC-SDS mixed micelle system are studied using conductivity measurement and a steady-state fluorescence technique. A series of water-soluble associative copolymers with acrylamide and DMDCC are prepared using the mixed micellar polymerization. Compared to conventional micellar polymerization, this new method could not only reasonably adjust the length of the hydrophobic microblock, that is, NH, but also sharply reduce the amount of surfactant. Their rheological properties related to hydrophobic microblock and stickers are studied by the combination of steady flow and linear viscoelasticity experiments. The results indicate that both the hydrophobic content and, especially the length of the hydrophobic microblock are the dominating factors effecting the intermolecular hydrophobic association. The presence of salt influences the dynamics of copolymers, resulting in the variation of solution characters. Viscosity measurement indicates that mixed micelles between the copolymer chain and SDS molecules serving as junction bridges for transitional network remarkably enhance the viscosity. Moreover, the microscopic structures of copolymers at different experimental conditions are conducted by ESEM. This method gives us an insight into the preparation of hydrophobically associative water-soluble copolymers by cationic surfmer-anionic surfactant mixed micellar polymerization with good performance.

  8. PREAPARATION OF CATIONIC LATEXES OF POLY(STYRENE-CO-BUTYL ACRYLATE) AND THEIR PROPERTIES EVOLUTION IN LATEX DILUTION

    Institute of Scientific and Technical Information of China (English)

    Dong Zou; Xiu-fen Li; Xiao-li Zhu; Xiang-zheng Kong

    2012-01-01

    Cationic latexes were prepared through emulsion copolymerization of styrene (St) and butyl acrylate (BA) with a cationic surfactant,cetyl trimethyl ammonium bromide (CTAB).Latex properties,including particle size,size distribution,ζ potential,surface tension and monomer conversion,were determined for latexes prepared with different CTAB amounts.Evolution of these properties during emulsion polymerization was followed in order to understand the mechanism of the particles formation.Results showed that both particle size and ζpotential were function of polymerization time and latex solids.Parallel emulsion polymerizations with cationic,anionic charged initiator and charge-free initiators were also carried out,the latex properties were determined at different polymerization time.All these results were attentively interpreted based on the mechanisms of emulsion polymerization,surfactant adsorption and latex particle stabilization.

  9. Preparation and characterization of nanocomposites of natural rubber with polystyrene and styrene-methacrylic acid copolymer nanoparticles

    Directory of Open Access Journals (Sweden)

    T. Nuruk

    2012-06-01

    Full Text Available Composites of natural rubber (NR/vinyl polymer nanoparticles as polystyrene (PS and poly(styrenemethacrylic acid (P(S-MAA were prepared by heterocoagulation technique. The polymer nanoparticles were prepared by emulsifier-free emulsion polymerizations at 70°C using potassium persulfate as initiator. Under acidic condition where positive charge was present on the NR latex (NRL surface, the nanoparticles having negative charge mainly from sulfate group of initiator were able to adsorb on the NRL surface, the electrostatic interaction being the driving force. The scanning electron micrographs showed that the polymer nanoparticles are homogenously distributed throughout NR matrix as nanoclusters with an average size of about 500 and 200 nm for PS and P(S-MAA, respectively. The mechanical properties of NR/PS and NR/P(S-MAA composite films were compared with the NR host. The nanocomposites, particularly when the polymer nanoparticles are uniformly dispersed, possess significantly enhanced mechanical properties strongly depending on the morphology of the nanocomposites.

  10. Managing latex allergies at home

    Science.gov (United States)

    ... proteins that are in latex. These foods include: Bananas Avocado Chestnuts Other foods that are less strongly ... Asthma and Immunology. Latex Cross-reactive Foods Fact Sheet. Updated October 8, 2015. latexallergyresources.org/latex-cross- ...

  11. Latex allergies - for hospital patients

    Science.gov (United States)

    ... proteins that are in latex. These foods include bananas, avocado, and chestnuts. Foods that are less strongly ... Asthma and Immunology. Latex Cross-reactive Foods Fact Sheet. Updated October 8, 2015. latexallergyresources.org/latex-cross- ...

  12. Natural rubber latex allergy

    Directory of Open Access Journals (Sweden)

    Deval Ravi

    2008-01-01

    Full Text Available Natural rubber latex (NRL is a ubiquitous allergen as it is a component of > 40,000 products in everyday life. Latex allergy might be attributed to skin contact or inhalation of latex particles. Latex allergy is an IgE-mediated hypersensitivity to NRL, presenting a wide range of clinical symptoms such as angioedema, swelling, cough, asthma, and anaphylactic reactions. Until 1979, latex allergy appeared only as type IV delayed hypersensitivity; subsequently, the proportion of different allergy types drifted towards type IV contact allergy reactions. Several risk factors for sensitization to NRL are already known and well documented. Some authors have established a positive correlation between a history of multiple surgical interventions, atopy, spina bifida malformation, and latex allergy incidence. We suspect an increase in latex allergy incidence in association with increased atopy and sensitivity to environmental allergens in the industrial population. It is often postulated in literature that the groups of workers at risk for this allergy are essentially workers in the latex industry and healthcare professionals. In this population, direct internal and mucosal contact with NRL medical devices may be the route of sensitization as factors such as the number of procedures and use of NRL materials (catheters and tubes were associated with increased risk of latex sensitization and allergy.

  13. Switchable pH-responsive polymeric membranes prepared via block copolymer micelle assembly.

    Science.gov (United States)

    Nunes, Suzana P; Behzad, Ali Reza; Hooghan, Bobby; Sougrat, Rachid; Karunakaran, Madhavan; Pradeep, Neelakanda; Vainio, Ulla; Peinemann, Klaus-Viktor

    2011-05-24

    A process is described to manufacture monodisperse asymmetric pH-responsive nanochannels with very high densities (pore density >2 × 10(14) pores per m(2)), reproducible in m(2) scale. Cylindric pores with diameters in the sub-10 nm range and lengths in the 400 nm range were formed by self-assembly of metal-block copolymer complexes and nonsolvent-induced phase separation. The film morphology was tailored by taking into account the stability constants for a series of metal-polymer complexes and confirmed by AFM. The distribution of metal-copolymer micelles was imaged by transmission electron microscopy tomography. The pH response of the polymer nanochannels is the strongest reported with synthetic pores in the nm range (reversible flux increase of more than 2 orders of magnitude when switching the pH from 2 to 8) and could be demonstrated by cryo-field emission scanning electron microscopy, SAXS, and ultra/nanofiltration experiments.

  14. Bioinert membranes prepared from amphiphilic poly(vinyl chloride)-g-poly(oxyethylene methacrylate) graft copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Patel, Rajkumar [Department of Chemical and Biomolecular Engineering, Yonsei University, 262 Seongsanno, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Patel, Madhumita [Department of Life Science, Dongguk University-Seoul, 3–26 Phil-dong, Chung-gu, Seoul 100-715 (Korea, Republic of); Ahn, Sung Hoon [Department of Chemical and Biomolecular Engineering, Yonsei University, 262 Seongsanno, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Sung, Yong Kiel [ReSEAT Program, Korea Institute of Science and Technology Information, 206-9 Cheongyangni-dong, Dongdaemun-gu, Seoul 130-742 (Korea, Republic of); Lee, Hyung-Keun [Korea Institute of Energy Research, 71-2 Jang-dong, Yuseong-gu, Dae-jeon 305-343 (Korea, Republic of); Kim, Jong Hak, E-mail: jonghak@yonsei.ac.kr [Department of Chemical and Biomolecular Engineering, Yonsei University, 262 Seongsanno, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Sung, Jung-Suk, E-mail: sungjs@dongguk.edu [Department of Life Science, Dongguk University-Seoul, 3–26 Phil-dong, Chung-gu, Seoul 100-715 (Korea, Republic of)

    2013-04-01

    Poly(vinyl chloride) (PVC) membrane was hydrophilically modified by grafting with poly(oxyethylene methacrylate) (POEM) using atom transfer radical polymerization (ATRP). The successful grafting of PVC main chain by POEM was characterized by Fourier transform infrared spectroscopy (FT-IR). The molecular weight and hydrophilicity of membranes increased with the amount of POEM grafting, as characterized by gel permeation chromatography (GPC) and contact angle measurement, respectively. Transmission electron microscope (TEM) and small angle X-ray scattering (SAXS) analysis revealed the microphase-separated structure of PVC-g-POEM and the domain spacing increased from 59.3 to 86.1 nm with increasing grafting degree. Scanning electron microscopy (SEM) was used for the direct visualization of the mouse embryonic fibroblast (MEF) cell and bacteria adhesion on the membrane surface. Protein adsorption and eukaryotic and prokaryotic cell adhesion tests showed that the bioinert properties of membranes were significantly increased with POEM content. Highlights: ► TEM and SAXS analysis revealed the microphase-separated structure of graft copolymer membranes. ► Protein adsorption and eukaryotic and prokaryotic cell adhesion tests were performed on graft copolymer membranes. ► Boinert properties of membranes were significantly increased with POEM content.

  15. Preparation of a pH-sensitive polyacrylate amphiphilic copolymer and its application in cellulase immobilization.

    Science.gov (United States)

    Liang, Wenjuan; Cao, Xuejun

    2012-07-01

    P(MDB), a pH-sensitive and reversible water-soluble copolymer, was synthesized with methacrylic acid (MAA), 2-(dimethylamino) ethyl methacrylate (DMAEMA), and butyl methacrylate (BMA) and used as carrier for cellulase. The copolymer is insoluble between pH 2.5 and 4.1, and soluble below pH 2.5 or above 4.1. Its recovery in aqueous solution was 97.2% by adjusting its isoelectric point (pI) to 3.1. Cellulase was covalently immobilized on P(MDB) with 1-ethyl-3-(3-dimethyllaminopropyl) carbodiimide. Under optimized conditions, the activity yield of immobilized cellulase was 63.24% and its recovery was 96.8% by adjusting the pI to 3.5. Maximum activity of the immobilized cellulase was achieved at 60 °C (pH 5.0), while free cellulase exhibited maximum activity at 55 °C (pH 5.0). The immobilized cellulase retained 83.1% of its initial activity after repeated five cycles of hydrolysis reaction. P(MDB) is a promising carrier for immobilizing enzymes with high and low optimum pH due to its dissolving characteristics.

  16. Switchable pH-responsive polymeric membranes prepared via block copolymer micelle assembly

    KAUST Repository

    Nunes, Suzana Pereira

    2011-05-24

    A process is described to manufacture monodisperse asymmetric pH-responsive nanochannels with very high densities (pore density >2 × 10 14 pores per m2), reproducible in m2 scale. Cylindric pores with diameters in the sub-10 nm range and lengths in the 400 nm range were formed by self-assembly of metal-block copolymer complexes and nonsolvent-induced phase separation. The film morphology was tailored by taking into account the stability constants for a series of metal-polymer complexes and confirmed by AFM. The distribution of metal-copolymer micelles was imaged by transmission electron microscopy tomography. The pH response of the polymer nanochannels is the strongest reported with synthetic pores in the nm range (reversible flux increase of more than 2 orders of magnitude when switching the pH from 2 to 8) and could be demonstrated by cryo-field emission scanning electron microscopy, SAXS, and ultra/nanofiltration experiments. © 2011 American Chemical Society.

  17. Preparation and Characterization of Lignin Graft Copolymer as a Filtrate Loss Control Agent for the Hydrocarbon Drilling Industry

    Directory of Open Access Journals (Sweden)

    Mohamad Nasir Mohamad Ibrahim

    2014-01-01

    Full Text Available Lignin graft copolymer (LGC was prepared using an addition polymerization technique that involved grafting a 2-acrylamido-2-methylpropane sulfonic acid (AMPS monomer onto soda lignin (SL. The optimal polymerization conditions were found to be as follows: soda lignin, 2.0 g; initiator, 3% (w/w potassium persulphate of SL; mass ratio of AMPS to SL, 1:2; reaction time, 7 h; and reaction temperature, 60 °C. The LGC was characterized using a Fourier transform infrared (FTIR spectroscopy, a thermogravimetric analyzer (TGA, and gel permeation chromatography (GPC. The filtrate loss controlling ability of the LGC was evaluated using the American Petroleum Institute Recommended Practice 13-B 1 standard procedures. The results showed that the LGC has remarkable rheological and filtration controlling properties at both room temperature and high aging temperatures (190 °C.

  18. Preparation of Cationic Soap-Free Fluorinated Styrene-Acrylate Latex with Core-Shell Sturcture and Its Nucleation Mechanism%阳离子无皂含氟核壳苯丙乳液的制备及成核机理

    Institute of Scientific and Technical Information of China (English)

    徐桂龙; 梁云; 杨进; 皮丕辉; 文秀芳; 杨卓如

    2012-01-01

    在水溶性阳离子单体甲基丙烯酰氧基乙基三甲基氯化铵(DMC)存在下,以乙醇为助溶剂,通过种子半连续核壳乳液聚合法制备阳离子无皂含氟核壳苯丙乳液。考察了水溶性阳离子单体DMC和乙醇用量对乳液聚合过程的影响;用透射电镜(TEM)和X射线光电子能谱(XPS)对聚合物乳液乳胶粒形貌及涂膜化学组成进行表征,并讨论了无皂乳液聚合的成核机理和聚合过程。结果表明,采用种子半连续乳液聚合法,当DMC的质量分数为6.0%,乙醇的质量分数为7.5%(釜液)时,可以得到稳定的阳离子核壳结构含氟乳液,无皂乳液聚合的成核机理是先以均相成核方式后继续以低聚物成核方式进行,最终形成核壳结构。%Soap-free cationic fluorinated poly-styrene-acrylate latex particles with core-shell structure were synthesized by seeded semi-continues emulsion polymerization using ethanol as co-solvent in the presence of water soluble cationic monomer methacryloxyethyltrimethyl ammonium chloride (DMC). The effects of DMC dosage and ethanol content on the stability of polymerization were studied. The surface element composition of the prepared copolymer film was analyzed by X-ray photoelectron spectroscopy (XPS), and the micro-structure of the prepared latex particles were observed by transmission electron microscopy (TEM). The nucleation mechanism of emulsion tx~lymerization was discussed based on the experimental results. The result shows that cationic soap-free fluorinated poly-styrene-acrylate emulsion with a core-shell structure can be prepared when the monomer DMC is 6.0 % and the ethanol is 7. 5%. The nucleation mechanism of emulsion polymerization is the combination of a homogeneous nucleation and micelle nucleation mechanism.

  19. Preparation of dual-sensitive graft copolymer hydrogel based on N-maleoyl-chitosan and poly(N-isopropylacrylamide) by electron beam radiation

    Indian Academy of Sciences (India)

    Jinchen Fan; Jie Chen; Liming Yang; Han Lin; Fangqi Cao

    2009-10-01

    Organic solvent-soluble N-maleoyl-chitosan (NMCS) was synthesized by reaction of chitosan with maleic anhydride (MAH) in N,N-dimethylformamide (DMF). N-maleoyl-chitosan-graft-poly(N-isopropylacrylamide) (NMCS-g-PNIPAAm) copolymer hydrogel was prepared via free radical polymerization by electron beam (EB) irradiation. The copolymer obtained was analysed by FT–IR, XRD and thermal gravimetric analysis (TGA). It was found that the grafting yield and grafting efficiency increased with increasing radiation absorbed dose and monomer amount, and then decreased. The swelling ratio of the copolymer hydrogel was low at pH 4–5, and LCST of the hydrogel was around 32°C.

  20. THERMOSENSITIVE POLYION COMPLEX MICELLES PREPARED BY SELF-ASSEMBLY OF TWO OPPOSITELY CHARGED DIBLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    Pan He; Chang-wen Zhao; Chun-sheng Xiao; Zhao-hui Tang; Xue-si Chen

    2013-01-01

    Polyion complex (PIC) micelles were spontaneously formed in aqueous solutions through electrostatic interaction between two oppositely charged block copolymers,poly(N-isopropylacrylamide)-b-poly(L-glutamic acid) and poly(N-isopropylacrylamide)-b-poly(L-lysine).Their controlled synthesis was achieved via the ring opening polymerization of N-carboxyanhydrides (NCA),ε-benzyloxycarbonyl-L-lysine (Lys(Z)-NCA) or γ-benzyl-L-glutamate (BLG-NCA) with amino-terminated poly(N-isopropylacrylamide) macroinitiator and the subsequent deprotection reaction.The formation of PIC micelles was confirmed by dynamic light scattering and transmission electron microscopy.Turbidimetric characterization suggested that the formed PIC micelles had a concentration-dependent thermosensitivity and their phase transition behaviors could be easily adjusted either by the block length of coplymers or the concentration of micelles.

  1. Preparation and Characterization of Aromatic Polybenzoxazoles Copolymers Containing 2,6-Naphthalene Units

    Institute of Scientific and Technical Information of China (English)

    LI Lei; FAN Xing-he; ZHAO Xiao-dong; ZHOU Jing-lun; CHEN Xiao-fang; WAN Xin-hua; ZHOU Qi-feng

    2004-01-01

    A series of polybenzoxazoles (co)polymers bearing crankshaft units in the main chain was synthesized by the conventional solution polycondensation of 4, 6-diaminorescinol dihydrochloride, terephthalic acid (TA)and 2,6-naphthalene dicarboxylic acid(NDA). All of the polymers show lyotropic liquid crystal behavior in polyphosphoric acid(PPA) and methanesulfonic acid (MSA). The polybenzoxazoles exhibit an excellent thermal resistance although the crankshaft monomer has been introduced into the polymer backbone. The temperature for the 5% weight loss of all the polymers is above 600 ℃. The X-ray diffraction analysis results show that the series of the polymers has a high crystallinity. The introduction of NDA makes a slight decrease in the thermal resistance of the polymers. The maximum absorption peak in the UV-Vis spectra can be adjusted according to the amount of 2,6-naphthalene units in the polymers, which indicates the potential application of the polymers as optoelectric materials.

  2. Basic butylated methacrylate copolymer/kappa-carrageenan interpolyelectrolyte complex: preparation, characterization and drug release behaviour.

    Science.gov (United States)

    Prado, H J; Matulewicz, M C; Bonelli, P; Cukierman, A L

    2008-09-01

    The formation of a novel interpolyelectrolyte complex (IPEC) between basic butylated methacrylate copolymer and kappa-carrageenan was investigated and the product formed was characterized. Turbidity measurements and elemental analyses pointed to a 1:1 interaction of the repeating units. These results and FT-IR confirmed IPEC formation. Electronic microscopy images, particle size determination by image analysis and N(2) (77K) adsorption measurements were consistent with a porous material. This IPEC formed presented very good flowability and compactibility. Two maxima were observed in the swelling behaviour as a function of pH. The performance of the IPEC as a matrix for controlled release of drugs was evaluated, using ibuprofen as a model drug. Release profiles were properly represented by a mathematical model, which indicates that the system releases ibuprofen in a zero-order manner. These profiles could be controlled by conveniently modifying the proportion of the IPEC in the tablets.

  3. 微波辐射制备室温自交联含氟聚丙烯酸酯乳液%Preparation of room temperature self-crosslinking fluorinated polyacrylate latex under microwave radiation

    Institute of Scientific and Technical Information of China (English)

    严微; 黄丽君; 王丽; 徐明; 徐祖顺

    2012-01-01

    Room temperature self-crosslinking fluorinated polyacrylate latex was prepared under microwave irradiation with dodecafluoroheptyl methacrylate (DAAM) as fluorine-containing monomer, diactone acrylamide as functional monomer, adipic dihydrazide as crosslinking agent, anionic sodium dodecyl sulfate and non-ionic aliphatic alcohol polyoxyethylene ether as composite emulsifier, and potassium persulfate as initiator. The impact of the crosslinking monomer amount on the conversion of monomers, particle size distribution and its index of the latex and water absorption of the latex film were studied. The latex formed in the shape of spherical particles with average diameter of 60-70 nm when the mass content of DAAM was 5%. As the DAAM content augmented the water absorption of the latex film decreased and in the meantime, the crosslinking played a leading role. However, if the DAAM content continued to rise, the water absorption of the latex film increased instead meanwhile the hydrophilic property took over the dominant role.%在微波辐射下,以甲基丙烯酸十二氟庚酯(DAAM)为含氟单体,双丙酮丙烯酰胺为功能单体,己二酸二酰肼为交联剂,阴离子十二烷基硫酸钠和非离子脂肪醇聚氧乙烯醚为复合乳化剂,在过硫酸钾的引发下,制备了可室温自交联的含氟聚丙烯酸酯乳液.考察了交联单体用量对转化率、粒径分布及分布指数和乳胶膜吸水率的影响.w(DAAM)为5%时,乳液乳胶粒呈球形,平均粒径在60~70 nm.随着DAAM用量的增加,乳胶膜吸水率减小,此时交联起主导作用;进一步增加DAAM用量,乳胶膜吸水率反而增大,此时亲水性起主导作用.

  4. Preparation and characterization of PEG-PPG-PEG copolymer/pregelatinized starch blends for use as resorbable bone hemostatic wax.

    Science.gov (United States)

    Suwanprateeb, J; Suvannapruk, W; Thammarakcharoen, F; Chokevivat, W; Rukskul, P

    2013-12-01

    In this study, polymer blends between PEG-PPG-PEG copolymer mixtures and pregelatinized starch at various compositions ranging from 0 to 3 % by weight were prepared and evaluated for potential use as novel resorbable bone hemostatic wax. It was found that the prepared samples had sufficient smearability for use as a bone wax. An addition of pregelatinized starch increased the hardness, smoothness and consistency of the texture while decreasing the adherence to glove. Thermal analysis indicated that the heat of fusion slightly decreased with increasing pregelatinized starch content. Compressive stiffness tended to decrease with increasing starch content for concentrations lower than 20 %, but re-increased at higher starch levels. In contrast, adherence deformation increased initially, but then decreased with increasing starch content. This behavior was related to the dependence of softening or reinforcing effect on the level of starch concentration in the samples. Adherence load and energy decreased with the addition of pregelatinized starch implying the decrease in adhesiveness of the samples. Furthermore, increasing the pregelatized starch amount also increased the liquid sealing duration of the samples at both 23 and 37 °C. Cytotoxicity tests against osteoblasts using a MTT assay revealed that the all the prepared samples and their raw materials did not show any cytotoxic potential. Formulations containing pregelatinized starch content between 20 and 30 % were found to show optimized performance.

  5. One-pot preparation of new copolymer electrolytes with tunable network structure for all-solid-state lithium battery

    Science.gov (United States)

    Chen, Bo; Xu, Qiang; Huang, Zhen; Zhao, Yanran; Chen, Shaojie; Xu, Xiaoxiong

    2016-11-01

    A new class of copolymer electrolytes with tunable network structure is successfully designed and prepared via a facile one-pot reaction. The trimethylolpropane triglycidyl ether (TMPEG) is cross-linked with poly (ethylene glycol) diamine (NPEG) to create well-defined solid network polymer electrolyte (SNPE). The network structure could be tuned by changing the molar ratio of TMPEG and NPEG or the molecular weight of NPEG. The effects of molecular weight of NPEG and molar ratio of EO/Li+ on the ionic conductivity are systematically investigated. The optimal electrolyte TMPEG-NPEG4K[2:1]-16:1 presents a maximum conductivity of 1.10 × 10-4 S cm-1 under 30 °C, and an 18-fold ionic conductivity enhancement in that of PEO-based electrolyte. Furthermore, it also exhibits wide electrochemical window (0-5.4 V), excellent compatibility with metallic Li, and superior mechanical properties. The all-solid-state lithium batteries LiFePO4/Li are assembled with TMPEG-NPEG4K[2:1]-16:1 electrolyte, and present good cycling and rate performance under 60 °C. The initial discharge specific capacities of the batteries are 161.7 mAh g-1 at 0.2 C and 132.7 mAh g-1 at 1 C, and the capacity retention ratio can be retained at 90.6% and 90.5% after 100 cycles. This new copolymer electrolyte may become a promising candidate for applications in all-solid-state lithium battery.

  6. 纤维素纳米纤维-丁苯胶乳复合材料的制备与表征%Preparation and characterization of cellulose-nanoifbers/styrene-butadiene latex (NFs/SBL) composites

    Institute of Scientific and Technical Information of China (English)

    宋冰; 石勇; 陆海龙; 马金霞; 周小凡

    2016-01-01

    采用共混法制备不同纤维素纳米纤维含量的纤维素纳米纤维-丁苯胶乳复合材料,并通过拉伸性能、扫描电镜、热重分析以及红外光谱检测该复合材料的相关性能。分析结果表明:纤维素纳米纤维能均匀分散在丁苯胶乳溶液中,对丁苯胶乳有较好的补强效果;和丁苯胶乳相比,制得复合材料的裂断伸长率增大,弹性变好;但纤维素纳米纤维的加入对丁苯胶乳热稳定性的影响不明显。%Cellulose-nanofibers/styrene-butadiene latex(NFs-SBL) composites were prepared by blending different amount of cellulose nanofibers with styrene-butadiene latex(SBL), through the tensile properties testing, scanning electron microscopy (SEM), thermo-gravimetric analysis and infrared spectrometric analysis(FT-IR). The result showed that NFs are dispersed uniformly in styrene-butadiene latex and showed a good reinforcing effect on SBL, composite material breaking elongation increased and elastic becoming good. However, the addition of NFs had a less impact on thermal stability of styrene-butadiene latex.

  7. Preparation and Film Performance of Self-Crosslinking Fluorine-Containing Latex at Room Temperature%室温自交联含氟乳液的制备及涂膜性能

    Institute of Scientific and Technical Information of China (English)

    秦总根; 涂伟萍; 夏正斌; 沈良军

    2005-01-01

    A kind of fluorine-containing latex was prepared by means of semicontinuous emulsion polymerization and self-crosslinked at ambient temperature. Various factors affecting the performance of the latex film, such as the N-MA content (mass fraction, the same below), the film formation temperature, the content of the fluorinecontaining monomer and the film thickness, were then studied. Moreover, the glass transition temperature and the surface property of the film were respectively determined by means of DSC analysis and Wilhelmy method.The weatherability of the fluorine-containing polymer was also investigated by the artificial accelerated ageing test. The results show that the performance to price ratio of the obtained latex is better than those of the fluorinecontaining latexes on the market.%采用半连续乳液聚合方法制备了一种室温自交联合氟乳液,对影响含氟乳液涂膜性能的因素如 N-MA含量(质量分数,下同)、成膜温度、含氟单体的用量及涂膜厚度等进行了分析.采用DSC法对乳液涂膜 的玻璃化温度进行了测定,用Wilhelmy方法对膜的表面性能进行了表征,并通过人工加速老化实验来考察 膜的耐老化性能.结果表明,所制得的乳液的性价比优于市场上的含氟乳液.

  8. Latex in the Hospital Environment

    Science.gov (United States)

    LATEX in the Hospital Environment Updated Fall 2015 This list provides a guide to some of the most common objects containing latex and offers some ... remover–Sepha Pharm) 1 LATEX in the Hospital Environment (continued) Frequently contains LATEX OR/Infection Control masks, ...

  9. Preparation and properties of BSA-loaded microspheres based on multi-(amino acid) copolymer for protein delivery.

    Science.gov (United States)

    Chen, Xingtao; Lv, Guoyu; Zhang, Jue; Tang, Songchao; Yan, Yonggang; Wu, Zhaoying; Su, Jiacan; Wei, Jie

    2014-01-01

    A multi-(amino acid) copolymer (MAC) based on ω-aminocaproic acid, γ-aminobutyric acid, L-alanine, L-lysine, L-glutamate, and hydroxyproline was synthetized, and MAC microspheres encapsulating bovine serum albumin (BSA) were prepared by a double-emulsion solvent extraction method. The experimental results show that various preparation parameters including surfactant ratio of Tween 80 to Span 80, surfactant concentration, benzyl alcohol in the external water phase, and polymer concentration had obvious effects on the particle size, morphology, and encapsulation efficiency of the BSA-loaded microspheres. The sizes of BSA-loaded microspheres ranged from 60.2 μm to 79.7 μm, showing different degrees of porous structure. The encapsulation efficiency of BSA-loaded microspheres also ranged from 38.8% to 50.8%. BSA release from microspheres showed the classic biphasic profile, which was governed by diffusion and polymer erosion. The initial burst release of BSA from microspheres at the first week followed by constant slow release for the next 7 weeks were observed. BSA-loaded microspheres could degrade gradually in phosphate buffered saline buffer with pH value maintained at around 7.1 during 8 weeks incubation, suggesting that microsphere degradation did not cause a dramatic pH drop in phosphate buffered saline buffer because no acidic degradation products were released from the microspheres. Therefore, the MAC microspheres might have great potential as carriers for protein delivery.

  10. Occupational allergies caused by latex.

    Science.gov (United States)

    Ahmed, Debra D Fett; Sobczak, Steven C; Yunginger, John W

    2003-05-01

    Allergy to natural rubber latex is an important cause of occupational allergy in healthcare workers. Disposable medical gloves are the major reservoir of latex allergens, particularly powdered gloves, in healthcare delivery settings. Diagnosis of latex allergy requires a history of exacerbation of cutaneous, respiratory, ocular, or systemic signs and symptoms after exposure to natural rubber latex products; and evidence of sensitization by patch testing, skin testing, measurement of latex-specific IgE antibodies, or challenge testing. Optimal management of latex allergy involves education concerning cross-reacting allergens, reduction of cutaneous or mucosal contact with dipped rubber products, and minimization of exposure to latex aeroallergens in work environments.

  11. Water soluble graft copolymer ({kappa}-carrageenan-g-N-vinyl formamide): preparation, characterization and application

    Energy Technology Data Exchange (ETDEWEB)

    Mishra, M.M.; Yadav, M.; Sand, A.; Tripathy, J.; Behari, K. [University of Allahabad, Allahabad (India). Dept. of Chemistry

    2010-03-25

    {kappa}-Carrageenan-g-N-vinyl formamide was synthesized by free radical initiation using the potassium monopersulphate (PMS)/malonic acid redox pair in an inert atmosphere. The effects of variation of different reactant oil grafting parameters have been studied by varying the concentration. Grafting ratio, add on and conversion showed an increasing trend on increasing the concentration of N-vinyl formamide, malonic acid, kappa-carrageenart and the concentration of PMS from 6 x 10{sup -3} to 22 x 10{sup -3} mol dm{sup -3}. The optimum temperature and time for grafting of N-vinyl formamide onto {kappa}-carrageenan was found to be 40{sup o}C and 120 min, respectively. The metal ion sorption, swelling behaviour, flocculation and resistance to biodegradation properties have been studied. Flocculation capability of {kappa}-carrageenart and {kappa}-carrageenan-g-N-vinyl formamide for both coking and non-coking coals has been studied for the treatment of coal mine waste water. The graft copolymer was characterized by FT-IR spectroscopy and thermogravimetric analysis.

  12. Properties of Copolymers of Aspartic Acid and Aliphatic Dicarboxylic Acids Prepared by Reactive Extrusion

    Science.gov (United States)

    Aspartic acid may be prepared chemically or by the fermentation of carbohydrates. Currently, low molecular weight polyaspartic acids are prepared commercially by heating aspartic acid at high temperatures (greater than 220 degrees C) for several hours in the solid state. In an effort to develop a ...

  13. The heat-chill method for preparation of self-assembled amphiphilic poly(ε-caprolactone)-poly(ethylene glycol) block copolymer based micellar nanoparticles for drug delivery.

    Science.gov (United States)

    Payyappilly, Sanal Sebastian; Dhara, Santanu; Chattopadhyay, Santanu

    2014-04-07

    A new method is developed for preparation of amphiphilic block copolymer micellar nanoparticles and investigated as a delivery system for celecoxib, a hydrophobic model drug. Biodegradable block copolymers of poly(ethylene glycol) (PEG) and poly(ε-caprolactone) (PCL) were synthesized by ring opening copolymerization and characterized thoroughly using FTIR, (1)H NMR and GPC. The block copolymer was dispersed in distilled water at 60 °C and then it was chilled in an ice bath for the preparation of the micellar nanoparticles. Polymers self-assembled to form micellar nanoparticles (HR-TEM, DLS and DSC. The cytotoxicity of the polymer micellar nanoparticles was investigated against HaCaT cell lines. The study of celecoxib release from the micellar nanoparticles was carried out to assess their suitability as a drug delivery vehicle. Addition of the drug to the system at low temperature is an added advantage of this method compared to the other temperature assisted nanoparticle preparation techniques. In a nutshell, polymer micellar nanoparticles prepared using the heat-chill method are believed to be promising for the controlled drug release system of labile drugs, which degrade in toxic organic solvents and at higher temperatures.

  14. From polymer latexes to multifunctional liquid marbles.

    Science.gov (United States)

    Fernandes, Ana M; Mantione, Daniele; Gracia, Raquel; Leiza, Jose R; Paulis, Maria; Mecerreyes, David

    2015-02-25

    A simple method to prepare multifunctional liquid marbles and dry water with magnetic, color, and fluorescent properties is presented. Multifunctional liquid marbles were prepared by encapsulation of water droplets using flocculated polymer latexes. First, the emulsion polymerization reaction of polystyrene and poly(benzyl methacrylate) was carried out using cheap and commercially available cationic surfactants. Subsequently, flocculation of the latex was provoked by an anion-exchange reaction of the cationic surfactant by the addition of lithium bis(trifluoromethanesulfonyl)imide salt. The flocculated polymer latex was filtered and dried, leading to very hydrophobic micronanoparticulated powders. These powders showed a great ability to stabilize the air/water interface. Stable liquid marbles were obtained by rolling water droplets onto the hydrophobic powders previously prepared. The use of very small polystyrene nanoparticles led us to the preparation of very stable and the biggest known liquid marbles up to 2.5 mL of water. Furthermore, the introduction of fluorescent comonomer dyes into the polymer powders allowed us to obtain new morphological images and new knowledge about the structure of liquid marbles by confocal microscopy. Furthermore, the introduction of magnetic nanoparticles into the polymer latex led to magnetic responsive liquid marbles, where the iron oxide nanoparticles are protected within a polymer. Altogether this method represents an accessible and general platform for the preparation of multifunctional liquid marbles and dry water, which may contribute to extending of their actual range of applications.

  15. Preparation of epoxy resin copolymers with low luminous decay%低光衰环氧树脂共聚物的制备

    Institute of Scientific and Technical Information of China (English)

    冯钠; 张小扉; 张桂霞; 陈涛; 王旭

    2011-01-01

    Copolymers of epoxy resin grafted by hydroxy-terminated silicone(EP-g-HTPDMS) with low luminous decay were prepared by graft condensation polymerization from EP and HTPDMS. The structure of the EP-g-HTPDMS copolymers was characterized by Fourier transform infrared spectroscopy(FTIR) and therm ogravimetric(TG) analysis. The EP-g-HTPDMS copolymers were applied to package of light-emitting diode, and its optical properties were studied by luminous decay and refractive index test. The mechanical properties and micro-morphology of the copolymers were analyzed by hardness tester and scanning electron microscope(SEM). The results indicate that HTPDMS is successfully incorporated into EP molecular chain.Adding HTPDMS has unobvious effect on the refractive index of the copolymers. When HTPDMS mass content is less than 9%, the relative light output of the EP-g-HTPDMS copolymers is higher than that of unmodified EP and luminous decay reduces significantly. The hardness of the copolymers decreases with increasing HTPDMS mass content. The introduction of HTPDMS makes the copolymer exhibit the features of tough fracture, lowers the internal stress in the system and improves the resistance to cracking.%采用接枝缩聚的方法,将端羟基硅酮(HTPDMS)与环氧树脂(EP)反应,制备低光衰HTPDMS接枝EP(EP-g-HTPDMS)共聚物.利用傅里叶变换红外光谱和热重分析表征其结构,并将制备的EP-g-HTPDMS共聚物应用于发光二级管封装,通过测试光衰和折射率分析其光学性能,同时利用硬度测试仪和扫描电子显微镜研究其力学性能和微观结构.结果表明:HTPDMS成功接枝在EP分子链中;引入HTPDMS对共聚物折射率的影响并不明显,当w(HTPDMS)小于9%时,共聚物的相对输出功率均高于EP,光衰明显降低;随着w(HTPDMS)增加,共聚物的硬度减小;引入HTPDMS使共聚物断面呈韧性断裂,体系的内应力降低,抗开裂性能得到改善.

  16. Lignin poly(lactic acid) copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Olsson, Johan Vilhelm; Chung, Yi-Lin; Li, Russell Jingxian; Waymouth, Robert; Sattely, Elizabeth; Billington, Sarah; Frank, Curtis W.

    2017-02-14

    Provided herein are graft co-polymers of lignin and poly(lactic acid) (lignin-g-PLA copolymer), thermoset and thermoplastic polymers including them, methods of preparing these polymers, and articles of manufacture including such polymers.

  17. Preparation of thermo-responsive graft copolymer by using a novel macro-RAFT agent and its application for drug delivery

    Energy Technology Data Exchange (ETDEWEB)

    Song, Cunfeng; Yu, Shirong [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Liu, Cheng; Deng, Yuanming; Xu, Yiting [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Fujian Provincial Key Laboratory of Fire Retardant Materials, Xiamen University, Xiamen 361005 (China); Chen, Xiaoling, E-mail: tinachen0628@163.com [Department of Endodontics, Xiamen Stomatology Hospital, Teaching Hospital of Fujian Medical University, Xiamen 361003 (China); Dai, Lizong, E-mail: lzdai@xmu.edu.cn [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Fujian Provincial Key Laboratory of Fire Retardant Materials, Xiamen University, Xiamen 361005 (China)

    2016-05-01

    A methodology to prepare thermo-responsive graft copolymer by using a novel macro-RAFT agent was proposed. The macro-RAFT agent with pendant dithioester (ZC(S)SR) was facilely prepared via the combination of RAFT polymerization and esterification reaction. By means of ZC(S)SR-initiated RAFT polymerization, the thermo-responsive graft copolymer consisting of poly(methyl methacrylate-co-hydroxylethyl methacrylate) (P(MMA-co-HEMA)) backbone and hydrophilic poly(N-isopropylacrylamide) (PNIPAAm) side chains was constructed through the “grafting from” approach. The chemical compositions and molecular weight distributions of the synthesized polymers were respectively characterized by {sup 1}H nuclear magnetic resonance ({sup 1}H NMR) and gel permeation chromatography (GPC). Self-assembly behavior of the amphiphilic graft copolymers (P(MMA-co-HEMA)-g-PNIPAAm) was studied by transmission electron microscopy (TEM), dynamic light scattering (DLS) and spectrofluorimeter. The critical micelle concentration (CMC) value was 0.052 mg mL{sup −1}. These micelles have thermo-responsibility and a low critical solution temperature (LCST) of 33.5 °C. Further investigation indicated that the guest molecule release property of these micelles, which can be well described by a first-order kinetic model, was significantly affected by temperature. Besides, the micelles exhibited excellent biocompatibility and cellular uptake property. Hence, these micelles are considered to have potential application in controlled drug delivery. - Highlights: • A novel macro-RAFT agent with ZC(S)SR was used for preparing graft copolymer. • P(MMA-co-HEMA)-g-PNIPAAm was successful prepared via the “grafting from” approach. • Thermo-responsibility of the P(MMA-co-HEMA)-g-PNIPAAm micelles was investigated. • The drug release behavior of the P(MMA-co-HEMA)-g-PNIPAAm micelles was studied. • These micelles exhibited excellent biocompatibility and cellular uptake property.

  18. Latex allergy (image)

    Science.gov (United States)

    ... dermatitis, or in a more serious whole body reaction, anaphylaxis. The term "dermatitis" describes an inflammatory response of the skin, caused by contact with allergens or irritants such as the latex ...

  19. Poly(Lactic Acid) Hemodialysis Membranes with Poly(Lactic Acid)-block-Poly(2-Hydroxyethyl Methacrylate) Copolymer As Additive: Preparation, Characterization, and Performance.

    Science.gov (United States)

    Zhu, Lijing; Liu, Fu; Yu, Xuemin; Xue, Lixin

    2015-08-19

    Poly(lactic acid) (PLA) hemodialysis membranes with enhanced antifouling capability and hemocompatibility were developed using poly(lactic acid)-block-poly(2-hydroxyethyl methacrylate) (PLA-PHEMA) copolymers as the blending additive. PLA-PHEMA block copolymers were synthesized via reversible addition-fragmentation (RAFT) polymerization from aminolyzed PLA. Gel permeation chromatography (GPC) and (1)H-nuclear magnetic resonance ((1)H NMR) were applied to characterize the synthesized products. By blending PLA with the amphiphilic block copolymer, PLA/PLA-PHEMA membranes were prepared by nonsolvent induced phase separation (NIPS) method. Their chemistry and structure were characterized with X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM) and atomic force microscopy (AFM). The results revealed that PLA/PLA-PHEMA membranes with high PLA-PHEMA contents exhibited enhanced hydrophilicity, water permeability, antifouling and hemocompatibility. Especially, when the PLA-PHEMA concentration was 15 wt %, the water flux of the modified membrane was about 236 L m(-2) h(-1). Its urea and creatinine clearance was more than 0.70 mL/min, lysozyme clearance was about 0.50 mL/min, BSA clearance was as less as 0.31 mL/min. All the results suggest that PLA-PHEMA copolymers had served as effective agents for optimizing the property of PLA-based membrane for hemodialysis applications.

  20. Effect of UV/ozone irradiation on the surface properties of electrospun webs and films prepared from polydimethylsiloxane-urea copolymers

    Science.gov (United States)

    Yilgor, Emel; Kaymakci, Orkun; Isik, Mehmet; Bilgin, Sevilay; Yilgor, Iskender

    2012-03-01

    Highly hydrophobic surfaces of silicone-urea copolymers were transformed into hydrophilic ones upon UV/ozone treatment. The extent of surface modification was strongly dependent on the sample preparation method and the exposure time. The physical and chemical changes at the copolymer surfaces were analyzed by spectroscopic (XPS, ATR-FTIR), microscopic (SEM) techniques and static water contact angle measurements. ATR-FTIR spectra clearly showed the dramatic change in the strongly hydrogen bonded urea hard segments and the degradation of dimethylsiloxane units in silicone-urea copolymers. XPS results revealed the formation of SiOx on the surface, which gradually increased with exposure time. After 3 h of UV/ozone exposure, Si(2p) binding energy shifted from 101.9 to 102.85 eV, which is a clear indication of an increase in the oxidation state of silicon. The deterioration of microroughness of the electrospun webs upon UV/ozone exposure, which was revealed by SEM, resulted in a dramatic decrease in the static water contact angle values from 129 to 62°. These results clearly show that UV/ozone process is a very simple and facile method to transform hydrophobic silicone-urea copolymer surfaces into fairly hydrophilic ones.

  1. Effect of UV/ozone irradiation on the surface properties of electrospun webs and films prepared from polydimethylsiloxane-urea copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Yilgor, Emel; Kaymakci, Orkun; Isik, Mehmet; Bilgin, Sevilay [Surface Science and Technology Center (KUYTAM), Chemistry Department, Koc University, Istanbul 34450 (Turkey); Yilgor, Iskender, E-mail: iyilgor@ku.edu.tr [Surface Science and Technology Center (KUYTAM), Chemistry Department, Koc University, Istanbul 34450 (Turkey)

    2012-03-01

    Highly hydrophobic surfaces of silicone-urea copolymers were transformed into hydrophilic ones upon UV/ozone treatment. The extent of surface modification was strongly dependent on the sample preparation method and the exposure time. The physical and chemical changes at the copolymer surfaces were analyzed by spectroscopic (XPS, ATR-FTIR), microscopic (SEM) techniques and static water contact angle measurements. ATR-FTIR spectra clearly showed the dramatic change in the strongly hydrogen bonded urea hard segments and the degradation of dimethylsiloxane units in silicone-urea copolymers. XPS results revealed the formation of SiO{sub x} on the surface, which gradually increased with exposure time. After 3 h of UV/ozone exposure, Si(2p) binding energy shifted from 101.9 to 102.85 eV, which is a clear indication of an increase in the oxidation state of silicon. The deterioration of microroughness of the electrospun webs upon UV/ozone exposure, which was revealed by SEM, resulted in a dramatic decrease in the static water contact angle values from 129 to 62 Degree-Sign . These results clearly show that UV/ozone process is a very simple and facile method to transform hydrophobic silicone-urea copolymer surfaces into fairly hydrophilic ones.

  2. Study on preparation and bonding properties of natural rubber latex grafted and modified by HEMA%HEMA接枝改性天然胶乳的制备及其粘接性能研究

    Institute of Scientific and Technical Information of China (English)

    卫飞云; 刘宏超; 曹端林; 余和平

    2013-01-01

    以甲基丙烯酸羟乙酯(HEMA)作为天然胶乳(NRL)的接枝改性剂,采用乳液聚合法制备了NR-g-HEMA[HEMA接枝NR(天然橡胶)]胶乳;然后以此为基体,并以水溶性松香树脂为增黏树脂、邻苯二甲酸二丁酯(DBP)为增塑剂等,制备相应的NR-g-HEMA胶粘剂;最后,用该胶粘剂压制胶合板,并对胶合板的粘接性能进行了测定.结果表明:采用单因素试验法优选出制备NR-g-HEMA胶乳的最佳工艺条件为m(干态单体)∶m(NRL)∶m(引发剂)∶m(活化剂)∶m(交联剂)=20∶100∶0.2∶0.2∶0.1、反应时间为8h和反应温度为16℃,此时相应胶合板的剪切强度(1.88MPa)符合Ⅲ类胶合板的指标要求.%Abstract:With hydroxyethyl methacrylate (HEMA) as graft modifier of natural rubber latex (NRL),a NR-g-HEMA[NR(natural rubber) grafted by HEMA] latex was prepared by emulsion polymerization.Then,with NR-g-HEMA latex as matrix,water-soluble rosin resin as tackifying resin,and dibutyl phthalate(DBP) as plasticizer,a corresponding NR-g-HEMA adhesive was prepared.Finally,the plywood was pressed by the adhesive,and the bongding properties of plywood were mensurated.The results showed that the optimal process conditions of preparing NR-g-HEMA latex were preferred by single-factor experiment method when mass ratio of m(dry monomer)∶m(NRL)∶m(initiator)∶m(activating agent)∶m(cross linker) was 20∶100∶0.2∶0∶2∶0.1,reaction time was 8h and reaction temperature was 16℃.Here,the shear strength (1.88MPa) of corresponding plywood could meet index requirement of Ⅲ class-plywood.

  3. Preparation and Properties of NR Composites by Latex Jet Mixing%射流胶乳混合法天然橡胶复合材料的制备及性能研究

    Institute of Scientific and Technical Information of China (English)

    韩晶杰; 张俊丽; 马玉录; 谢林生

    2014-01-01

    用射流胶乳混合法制备天然橡胶(NR)复合材料,并对复合材料性能进行研究。先用超声空化作用将炭黑团聚体破碎、切割、分散在水中制得炭黑悬浮液,然后在高速射流场中将炭黑微观分散到天然胶乳中制成NR复合材料。结果表明:与传统干法混炼工艺相比,射流胶乳混合工艺可以使炭黑更均匀地分散到NR基体中;射流胶乳混合工艺制备的复合材料硫化时间缩短,硫化程度增大,撕裂强度提高78%,回弹值提高20%,DIN磨耗量减小33%。%In this study, NR composites were prepared by latex jet mixing method and the properties of the composites were investigated. In the preparation process, ifrstly, the carbon black was dispersed in water by ultrasonic, and then in the ifeld of high speed jet, the pre-dispersed carbon black was mixed with NR latex to give the NR composites. Compared with the conventional blending process, carbon black was dispersed in NR matrix much better by using latex jet mixing process, the curing time of the compound was shortened, the degree of cure increased, the tear strength of the vulcanizate increased by 78%, the resilience was improved by 20%, and DIN abrasion loss decreased by 33%.

  4. Preparation of Al Fe{sub 2}O{sub 3} Core-Shell Composites Using Amphiphilic Graft Copolymer Template

    Energy Technology Data Exchange (ETDEWEB)

    Patel, Rajkumar; Kim, Sang Jin; Kim, Jin Kyu; Kim, Jong Hak [Yonsei University, Seoul (Korea, Republic of); Park, Jung Su [Agency for Defense and Development (ADD), Daejeon (Korea, Republic of)

    2014-04-15

    A graft copolymer of poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) was synthesized via atom transfer radical polymerization (ATRP) and used as a structure-directing agent to prepare Al Fe{sub 2}O{sub 3} core-shell nanocomposites through a sol-gel process. The amphiphilic property of PVC-g-POEM allows for good dispersion of Al particles and leads to specific interaction with iron ethoxide, a precursor of Fe{sub 2}O{sub 3}. Secondary bonding interaction in the sol-gel composites was characterized by Fourier transform-infrared (FT-IR) spectroscopy. The well-organized morphology of Al Fe{sub 2}O{sub 3} core-shell nanocomposites was observed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Energy dispersive X-ray (EDX) and X-ray diffraction (XRD) were used to analyze the elemental composition and crystallization structure of the composites.

  5. Degradable Polycaprolactone and Polylactide Homopolymer and Block Copolymer Brushes Prepared by Surface-Initiated Polymerization with Triazabicyclodecene and Zirconium Catalysts.

    Science.gov (United States)

    Grubbs, Joe B; Arnold, Rachelle M; Roy, Anandi; Brooks, Karson; Bilbrey, Jenna A; Gao, Jing; Locklin, Jason

    2015-09-22

    Surface-initiated ring-opening polymerization (SI-ROP) of polycaprolactone (PCL) and polylactide (PLA) polymer brushes with controlled degradation rates were prepared on oxide substrates. PCL brushes were polymerized from hydroxyl-terminated monolayers utilizing triazabicyclodecene (TBD) as the polymerization catalyst. A consistent brush thickness of 40 nm could be achieved with a reproducible unique crystalline morphology. The organocatalyzed PCL brushes were chain extended using lactide in the presence of zirconium n-butoxide to successfully grow PCL/PLA block copolymer (PCL-b-PLA) brushes with a final thickness of 55 nm. The degradation properties of "grafted from" PCL brush and the PCL-b-PLA brush were compared to "grafted to" PCL brushes, and we observed that the brush density plays a major role in degradation kinetics. Solutions of methanol/water at pH 14 were used to better solvate the brushes and increase the kinetics of degradation. This framework enables a control of degradation that allows for the precise removal of these coatings.

  6. Latex samples for RAMSES electrophoresis experiment on IML 2

    Science.gov (United States)

    Seaman, Geoffrey V. F.; Knox, Robert J.

    1994-01-01

    The objectives of these reported studies were to provide ground based support services for the flight experiment team for the RAMSES experiment to be flown aboard IML-2. The specific areas of support included consultation on the performance of particle based electrophoresis studies, development of methods for the preparation of suitable samples for the flight hardware, the screening of particles to obtain suitable candidates for the flight experiment, and the electrophoretic characterization of sample particle preparations. The first phases of these studies were performed under this contract, while the follow on work was performed under grant number NAG8 1081, 'Preparation and Characterization of Latex Samples for RAMSES Experiment on IML 2.' During this first phase of the experiment the following benchmarks were achieved: Methods were tested for the concentration and resuspension of latex samples in the greater than 0.4 micron diameter range to provide moderately high solids content samples free of particle aggregation which interferred with the normal functioning of the RAMSES hardware. Various candidate latex preparations were screened and two candidate types of latex were identified for use in the flight experiments, carboxylate modified latex (CML) and acrylic acid-acrylamide modified latex (AAM). These latexes have relatively hydrophilic surfaces, are not prone to aggregate, and display sufficiently low electrophoretic mobilities in the flight buffer so that they can be used to make mixtures to test the resolving power of the flight hardware.

  7. The preparation of polystyrene latex coated expanded perlite%聚苯乙烯乳液包膜膨胀珍珠岩的研制

    Institute of Scientific and Technical Information of China (English)

    孙义明; 毕小云; 谢霞

    2012-01-01

    将废聚苯乙烯泡沫制成乳液,用包衣机将其包膜在膨胀珍珠岩表面,形成一层柔性的聚合物膜,达到膨胀珍珠岩闭孔的效果,可有效地改善膨胀珍珠岩的吸水性,提高膨胀珍珠岩的强度,解决了闭孔膨胀珍珠岩在运输途中易破碎的问题.%This paper makes waste polystyrene into foam latex, using coating machine, makes Polystyrene latex coated expanded perlite surface.forms a layer of flexible polymer membrane, achieves the effect of closed pore, and effectively improves the expanded perlite water imbibition, improves the strength of the expansion perlite, and solves the easy broken problem of closed pore expansion perlite in transportation.

  8. Influencing Selectivity to Cancer Cells with Mixed Nanoparticles Prepared from Albumin-Polymer Conjugates and Block Copolymers.

    Science.gov (United States)

    Jiang, Yanyan; Wong, Sandy; Chen, Fan; Chang, Ted; Lu, Hongxu; Stenzel, Martina H

    2017-04-19

    Albumin-based nanoparticles are widely used to delivery anticancer drug because they promote the accumulation of drugs in tumor sites. Nanoparticles with surface immobilized albumin are widely described in literature, although mixed nanoparticles with systematically modified ratios between albumin and PEG-based material are less common. In this work, hybrid nanoparticles were prepared by coassembly of a PEG-based amphiphilic block copolymer together with a polymer-protein conjugate. Poly(oligo(ethylene glycol) methyl ether acrylate)-poly(ε-caprolactone) (POEGMEA-PCL) was prepared by a combination of ring-opening polymerization and reversible addition-fragmentation chain transfer (RAFT) polymerization, while the polymer-protein conjugate was obtained by reacting poly(ε-caprolactone) with bovine serum albumin (BSA-PCL). Co-assembly of both amphiphiles at different ratios, with and without curcumin as a drug, led to hybrid nanoparticles with various amount of albumin on the particle surface. The resulting hybrid nanoparticles were similar in size (100-120 nm), but increasing the amount of albumin on the surface led to a more-negative ζ potential. The cytotoxicity of the curcumin-loaded nanoparticles was examined on several cell lines. The curcumin-loaded nanoparticles with high amount of albumin led to high cytotoxicity against breast cancer cell lines (MDA-MB-231 and MCF-7), which coincided with high cellular uptake. However, the cytotoxicity of the curcumin-loaded nanoparticles against CHO cells and RAW264.7 cells was reduced, suggesting that albumin can facilitate selectivity toward cancer cells.

  9. Latex Allergy in Dental Care

    Directory of Open Access Journals (Sweden)

    Dermata A.

    2014-07-01

    Full Text Available Natural rubber latex is found in numerous medical and dental products. Adverse latex reactions in dental patients and practitioners have significantly increased since the introduction of universal precautions for infection control. These reactions range from contact dermatitis to potentially life-threatening hypersensitivity. Patients with a history of spina bifida, urogenital anomalies, multiple surgical procedures, allergic reactions or atopy, health care personnel and latex production workers are at increased risk of latex allergy. Diagnosis is based on a combination of clinical history and laboratory tests. Identification of latex sources and the avoidance of latex exposure are critical for protecting both dental patients and dental personnel.

  10. Preparation and self-assembly behavior of polystyrene-block-poly (dimethylaminoethyl methacrylate amphiphilic block copolymer using atom transfer radical polymerization

    Directory of Open Access Journals (Sweden)

    2008-03-01

    Full Text Available Asymmetric and semi-symmetric amphiphilic diblock copolymers polystyrene-block-poly (dimethylaminoethyl methacrylate (PS-b-PDMAEMA with the same PS block length of 62 repeat units and quite short (3 repeat units or equivalent (47 repeat units length of PDMAEMA have been prepared simply by varying the ratio of the bromine-terminated macroinitiator polystyrene (PS-Br to DMAEMA using atom transfer radical polymerization (ATRP. The chemical structures and compositions of the PS-b-PDMAEMA block copolymers are studied by nuclear magnetic resonance (NMR spectroscopy, gel permeation chromatography (GPC, and elementary analysis (EA. The self-assembly behaviors of copolymers in N,N-dimethyl formamide (DMF with different pH and dioxane/water binary solvent mixture by direct dissolution method (DD, are studied by transmission electron microscopy (TEM, electron diffracting analysis (EDA, and energy-dispersive analysis of X-rays (EDAX techniques. Transmission electron microscopy results suggest that asymmetric block copolymer PS62-b-PDMAEMA3 (the numbers in the form of footnotes represent repeated units of each monomer in the copolymer can form spherical core-shell micelles, large compound reverse micelles (LCRMs, hexagonal/rhombic phases, reverse hexagonal/rhombic phases, vesicles, reverse vesicles and necklace-like reverse micelles, controlled by common or selective solvent and pH, while most of the aggregates of semi-symmetric PS62-b-PDMAEMA47 are simply spherical, such as spherical core-shell micelles and reverse spherical core-shell micelles, besides hexagonal/rhombic phases. All above structures are controlled by three components of the free energy of aggregation: core-chain stretching, interfacial energy and intercoronal chain interaction.

  11. Preparation and flocculation properties of cationic starch/chitosan crosslinking-copolymer.

    Science.gov (United States)

    You, Lijun; Lu, Feifei; Li, Dan; Qiao, Zhongming; Yin, Yeping

    2009-12-15

    A novel flocculant (CATCS) based on corn starch and chitosan was prepared and its flocculation behaviors were studied. The synthesis conditions of CATCS were discussed and the production obtained was characterized using Fourier infrared spectra and scanning electron microscopy. Flocculation properties of the products were evaluated in terms of transmittance, removal of organic contaminant and solid suspending substances. Influences of temperature, pH and flocculant dosage on flocculation efficiency of CATCS were examined. CATCS had better flocculation performance at lower temperature for the wastewater investigated. CATCS showed better flocculation performance than cationic starch and chitosan in 5 g/L kaolin suspension trended to performance well in acidic and alkaline solution. The comparison of the flocculation performance between CATCS, Fe2(SO4)3 and polyacrylamide showed CATCS had much efficient flocculation performance. In addition, cationic starch was prepared from corn starch using microwave-assisted method.

  12. Preparation and flocculation properties of cationic starch/chitosan crosslinking-copolymer

    Energy Technology Data Exchange (ETDEWEB)

    You Lijun; Lu Feifei; Li Dan; Qiao Zhongming [Department of chemistry, College of Science, Huazhong Agricultural University, Wuhan, 430070 (China); Yin Yeping, E-mail: yljyoyo@yahoo.cn [Department of chemistry, College of Science, Huazhong Agricultural University, Wuhan, 430070 (China)

    2009-12-15

    A novel flocculant (CATCS) based on corn starch and chitosan was prepared and its flocculation behaviors were studied. The synthesis conditions of CATCS were discussed and the production obtained was characterized using Fourier infrared spectra and scanning electron microscopy. Flocculation properties of the products were evaluated in terms of transmittance, removal of organic contaminant and solid suspending substances. Influences of temperature, pH and flocculant dosage on flocculation efficiency of CATCS were examined. CATCS had better flocculation performance at lower temperature for the wastewater investigated. CATCS showed better flocculation performance than cationic starch and chitosan in 5 g/L kaolin suspension trended to performance well in acidic and alkaline solution. The comparison of the flocculation performance between CATCS, Fe{sub 2} (SO{sub 4}){sub 3} and polyacrylamide showed CATCS had much efficient flocculation performance. In addition, cationic starch was prepared from corn starch using microwave-assisted method.

  13. PREPARATION AND CHARACTERIZATION OF ORGANIC AEROGELS BY THE LIGNIN - RESORCINOL - FORMALDEHYDE COPOLYMER

    Directory of Open Access Journals (Sweden)

    Feng Chen

    2011-04-01

    Full Text Available Lignin can be used as a cheap natural raw material to prepare organic aerogels based upon gelation and supercritical drying in ethanol. The aerogels were prepared from a mixture of the raw materials with lignin (L, resorcinol (R, and formaldehyde (F, followed by a reaction catalyzed by NaOH(C. The effect of the preparation conditions, such as the LRF concentration, the mass ratio of LR to NaOH (LR/C, the mole ratio of LR to F (LR/F, and the gelation temperature, on the gelation ability and the bulk density were studied. The results showed that the density of LRF aerogels increased with increasing reactant concentration and catalyst content. The microstructure of the porous carbon aerogels was investigated by SEM and TEM. The specific surface area and pore size distribution of LRF and RF aerogels were studied by nitrogen adsorption-desorption analysis. The pore width of LRF aerogels ranged from 1 nm to 100 nm. Most of the pores were about 50 nm wide, as is typical for mesoporous materials.

  14. Preparation of thermo-responsive graft copolymer by using a novel macro-RAFT agent and its application for drug delivery.

    Science.gov (United States)

    Song, Cunfeng; Yu, Shirong; Liu, Cheng; Deng, Yuanming; Xu, Yiting; Chen, Xiaoling; Dai, Lizong

    2016-05-01

    A methodology to prepare thermo-responsive graft copolymer by using a novel macro-RAFT agent was proposed. The macro-RAFT agent with pendant dithioester (ZC(S)SR) was facilely prepared via the combination of RAFT polymerization and esterification reaction. By means of ZC(S)SR-initiated RAFT polymerization, the thermo-responsive graft copolymer consisting of poly(methyl methacrylate-co-hydroxylethyl methacrylate) (P(MMA-co-HEMA)) backbone and hydrophilic poly(N-isopropylacrylamide) (PNIPAAm) side chains was constructed through the "grafting from" approach. The chemical compositions and molecular weight distributions of the synthesized polymers were respectively characterized by (1)H nuclear magnetic resonance ((1)H NMR) and gel permeation chromatography (GPC). Self-assembly behavior of the amphiphilic graft copolymers (P(MMA-co-HEMA)-g-PNIPAAm) was studied by transmission electron microscopy (TEM), dynamic light scattering (DLS) and spectrofluorimeter. The critical micelle concentration (CMC) value was 0.052 mg mL(-1). These micelles have thermo-responsibility and a low critical solution temperature (LCST) of 33.5°C. Further investigation indicated that the guest molecule release property of these micelles, which can be well described by a first-order kinetic model, was significantly affected by temperature. Besides, the micelles exhibited excellent biocompatibility and cellular uptake property. Hence, these micelles are considered to have potential application in controlled drug delivery.

  15. DMFC Performance of Polymer Electrolyte Membranes Prepared from a Graft-Copolymer Consisting of a Polysulfone Main Chain and Styrene Sulfonic Acid Side Chains

    Directory of Open Access Journals (Sweden)

    Nobutaka Endo

    2016-08-01

    Full Text Available Polymer electrolyte membranes (PEMs for direct methanol fuel cell (DMFC applications were prepared from a graft-copolymer (PSF-g-PSSA consisting of a polysulfone (PSF main chain and poly(styrene sulfonic acid (PSSA side chains with various average distances between side chains (Lav and side chain lengths (Lsc. The polymers were synthesized by grafting ethyl p-styrenesulfonate (EtSS on macro-initiators of chloromethylated polysulfone with different contents of chloromethyl (CM groups, and by changing EtSS content in the copolymers by using atom transfer radical polymerization (ATRP. The DMFC performance tests using membrane electrode assemblis (MEAs with the three types of the PEMs revealed that: a PSF-g-PSSA PEM (SF-6 prepared from a graft copolymer with short average distances between side chains (Lav and medium Lsc had higher DMFC performance than PEMs with long Lav and long Lsc or with short Lav and short Lsc. SF-6 had about two times higher PDmax (68.4 mW/cm2 than Nafion® 112 at 30 wt % of methanol concentration. Furthermore, it had 58.2 mW/cm2 of PDmax at 50 wt % of methanol concentration because of it has the highest proton selectivity during DMFC operation of all the PSF-g-PSSA PEMs and Nafion® 112.

  16. Preparation of poly(vinyl phosphate-b-styrene) copolymers and its blend with PPO as proton exchange membrane for DMFC applications

    Energy Technology Data Exchange (ETDEWEB)

    Li, Guang Hua; Cho, Chang Gi [Center for Advanced Functional Polymers, Department of Fiber and Polymer Engineering, Hanyang University (Korea, Republic of); Lee, Chang Hyun; Lee, Young Moo [Department of Chemical Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of)

    2006-04-15

    Poly(vinyl phosphate-b-styrene) (poly(VPP-b-St)) block copolymers were prepared via consecutive telomerization of vinyl acetate (VAc), atom transfer radical polymerization (ATRP) with styrene, saponification, and phosphorylation with phosphorus oxychloride. The resulting block copolymers were characterized by FT-IR and pH titration. Then, the block copolymers were blended with poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) to prepare direct methanol fuel cell (DMFC) membrane. The performance of poly(VPP-b-St)/PPO blend membranes was measured in terms of proton conductivity, methanol permeability, thermal and hydrolytic stability. The proton conductivities were in the range of 10{sup -4} to 10{sup -2} S/cm (60C, RH=95%); the methanol permeabilities were in the range of 4.14x10{sup -8} to 9.62x10{sup -8} cm{sup 2}/s (25C), and quite lower than that of Nafion(R) 117. Also, the thermal stability of the blend membranes was characterized by TGA, and was stable up to 400C; the blend membranes had better hydrolytic stability. (author)

  17. Synthesis and self-assembly of Chitosan-g-Polystyrene copolymer: A new route for the preparation of heavy metal nanoparticles

    KAUST Repository

    Francis, Raju S.

    2015-01-01

    Amphiphilic graft copolymers made of a Chitosan (CS) backbone and three arm polystyrene (PS) grafts were prepared by "grafting onto" strategy using Toluene Diisocyanate. IR spectroscopy and SEC show the successful grafting process. SEM pictures of Chitosan-g-Polystyrene (CS-g-PS) indicate a spherulite like surface and exhibit properties that result from the disappearance of Chitosan crystallinity. The introduced polystyrene star grafts units improve hydrophobic properties considerably as confirmed by the very high solubility of (CS-g-PS) in organic solvents. The graft copolymer which self-assembles into polymeric micelles in organic media demonstrates much better adsorption of transition and inner transition metal ions than pure Chitosan whose amine groups are not necessarily available due to crystallinity.

  18. Synthesis and self-assembly of chitosan-g-polystyrene copolymer: a new route for the preparation of heavy metal nanoparticles.

    Science.gov (United States)

    Francis, Raju; Baby, Deepa K; Gnanou, Yves

    2015-01-15

    Amphiphilic graft copolymers made of a Chitosan (CS) backbone and three arm polystyrene (PS) grafts were prepared by "grafting onto" strategy using Toluene Diisocyanate. IR spectroscopy and SEC show the successful grafting process. SEM pictures of Chitosan-g-Polystyrene (CS-g-PS) indicate a spherulite like surface and exhibit properties that result from the disappearance of Chitosan crystallinity. The introduced polystyrene star grafts units improve hydrophobic properties considerably as confirmed by the very high solubility of (CS-g-PS) in organic solvents. The graft copolymer which self-assembles into polymeric micelles in organic media demonstrates much better adsorption of transition and inner transition metal ions than pure Chitosan whose amine groups are not necessarily available due to crystallinity.

  19. Blends of guayule natural rubber latex with commercial latex polymers

    Science.gov (United States)

    Guayule (Parthenium argentatum) is a woody desert shrub that produces natural rubber, cis-1,4 polyisoprene, by biosynthesis. It is currently cultivated in the southwestern United States as a source of latex and rubber for commercial development. Guayule latex is similar to Hevea latex in polymer mo...

  20. Microspheres prepared with different co-polymers of poly(lactic-glycolic acid) (PLGA) or with chitosan cause distinct effects on macrophages.

    Science.gov (United States)

    Bitencourt, Claudia da Silva; Silva, Letícia Bueno da; Pereira, Priscilla Aparecida Tartari; Gelfuso, Guilherme Martins; Faccioli, Lúcia Helena

    2015-12-01

    Microencapsulation of bioactive molecules for modulating the immune response during infectious or inflammatory events is a promising approach, since microspheres (MS) protect these labile biomolecules against fast degradation, prolong the delivery over longer periods of time and, in many situations, target their delivery to site of action, avoiding toxic side effects. Little is known, however, about the influence of different polymers used to prepare MS on macrophages. This paper aims to address this issue by evaluating in vitro cytotoxicity, phagocytosis profile and cytokines release from alveolar macrophages (J-774.1) treated with MS prepared with chitosan, and four different co-polymers of PLGA [poly (lactic-co-glycolic acid)]. The five MS prepared presented similar diameter and zeta potential each other. Chitosan-MS showed to be cytotoxic to J-774.1 cells, in contrast to PLGA-MS, which were all innocuous to this cell linage. PLGA 5000-MS was more efficiently phagocytized by macrophages compared to the other MS tested. PLGA 5000-MS and 5002-MS induced significant production of TNF-α, while 5000-MS, 5004-MS and 7502-MS decreased spontaneous IL-6 release. Nevertheless, only PLGA 5002-MS induced significant NFkB/SEAP activation. These findings together show that MS prepared with distinct PLGA co-polymers are differently recognized by macrophages, depending on proportion of lactic and glycolic acid in polymeric chain, and on molecular weight of the co-polymer used. Selection of the most adequate polymer to prepare a microparticulate drug delivery system to modulate immunologic system may take into account, therefore, which kind of immunomodulatory response is more adequate for the required treatment.

  1. The effect of pyrolytic carbon black prepared from junked tires on the properties of ethylene-propylene-diene copolymers (EPDM

    Directory of Open Access Journals (Sweden)

    2009-05-01

    Full Text Available Pyrolytic carbon black (PCB made from used tires was used in ethylene-propylene-diene copolymers (EPDM. The microstructure of PCB was characterized by scanning electron microscopy (SEM. PCB was compounded with EPDM to prepare EPDM vulcanizates. The effects of PCB on the processing properties of EPDM compounds and the mechanical properties of vulcanizates were investigated and compared with other traditional fillers such as semi-reinforcing furnace black (N774, light calcium carbonate (CaCO3 and thermal black (N990. At the same time, the rheological behavior of EPDM compounds filled with different fillers was characterized by capillary rheometrics. The SEM photos showed that the particle shape was quiet different from that of CaCO3 and N990, it was similar to that of N774. The primary particle size was smaller than that of N774, but the aggregate size of PCB was larger than that of N774. The effect of PCB on the processing properties of EPDM compounds was similar to that of other fillers. Among the four fillers, PCB imparted EPDM compounds with higher Mooney viscosity. With the increase of filler content, the scorch time and optimum curing time of EPDM compounds changed little. The reinforcing effect of PCB was similar to that of N990, but inferior to that of N774. With the increase of PCB content, tensile strength, tear strength, and modulus at 100% elongation of EPDM vulcanizates increased significantly. When EPDM was filled with 50 phr PCB, the tear strength of EPDM vulcanizates increased by 3 times, compared with that of EPDM gum vulcanizates. The appearance of EPDM extrudate filled with PCB was coarser than that of other fillers.

  2. Preparation and Properties of Ethylene Vinyl Acetate Copolymer/Silica Nanocomposites in Presence of EVA-g-Acrylic Acid.

    Science.gov (United States)

    Tham, Do Quang; Tuan, Vu Manh; Thanh, Dinh Thi Mai; Chinh, Nguyen Thuy; Giang, Nguyen Vu; Trang, Nguyen Thi Thu; Hang, To Thi Xuan; Huong, Ho Thu; Dung, Nguyen Thi Kim; Hoang, Thai

    2015-04-01

    Here we report a facile approach to enhance the dispersibility of ethylene vinyl acetate copolymer (EVA)/silica nanocomposites (for the EVA/silica nanocomposites and interaction between silica nanoparticles (nanosilica) and EVA by adding EVA-g-acrylic acid (EVAgAA) as a compatibilizer, which was formed by grafting acrylic acid onto EVA chains with the aid of dicumyl peroxide). The above nanocomposites with and without EVAgAA were prepared by melt mixing in a Haake intermixer with different contents of silica and EVAgAA. Their structure and morphology were characterized by Fourier transform infra-red (FT-IR) spectroscopy, field emission scanning electron microscopy (FE-SEM), and the mechanical, rheological, dielectrical, and flammability properties of the nanocomposites were also investigated. The FT-IR spectra of the nanocomposites confirmed the formation of hydrogen bonds between the surface silanol groups of nanosilica and C=O groups of EVA and/or EVAgAA. The presence of EVAgAA remarkably increased the intensity of hydrogen bonding between nanosilica and EVA which not only enhanced the dispersion of nanosilica in EVA matrix but also increased the mechanical, viscosity and storage modulus of EVA/silica nanocomposites. In addition, the flammability of EVA/silica nanocomposites is also significantly reduced after the functionalization with EVAgAA. However, the mechanical properties of EVA/silica nanocomposites tended to level off when its content was above 1.5 wt.%. It has also been found that the dielectric constant value of the EVA/EVAgAA/silica nanocomposites is much lower than that of the EVA/silica nanocomposites, which is another evidence of the hydrogen bonding formation between EVAgAA and nanosilica.

  3. 硅烷偶联剂改性水性丙烯酸酯乳液的制备及性能%Preparation and properties of waterborne organosilicone modified acrylate latex

    Institute of Scientific and Technical Information of China (English)

    张昭; 陈华; 樊国栋; 李阿峰; 赵琪; 李会宁

    2012-01-01

    A kind of adhesive emulsion was prepared by emulsion polymerization, in which methyl methacrylate, butyl acrylate, acrylic acid and methacryloxy propyl trimethoxyl silane (KH-570) as monomers, sodium dodecyl benzene sulfonate and alkylphenol ethoxylatesCOP-10) as emulsifiers, ammonium persulfate as initiator. The factors of influence on kinetics of emulsion polymerization were studied. FT-IR was used to confirm the molecule structure. TG was used to characterized latex film s heat stability. Surface properties of the latex film were measured by contact angle measurements. The results showed that the latex particle size was decreased with increasing emulsifier and initiator. Temperature had great effect on the rate of polymerization. The rate grew up dramatically with the increase of reaction temperature. The hydrophobic and oleophobic performance increased with increasing the concentration of KH-570. The latex modified by KH-570 had excellent thermal property.%以丙烯酸丁酯(BA)和甲基丙烯酸甲酯(MMA)、丙烯酸(AA)和γ-甲基丙烯酰氧基丙基三甲氧基硅烷(KH-570)为单体,过硫酸铵为引发剂,十二烷基苯磺酸钠(SDBS)和烷基酚聚氧乙烯醚(OP-10)为复合乳化剂,采用半连续乳液聚合法合成了复合胶黏剂乳液.采用红外光谱对聚合物结构进行了表征,热重分析研究了聚合物胶膜的热稳定性.接触角的测定表征了聚合物膜的表面性能.研究了反应温度,引发剂和乳化剂用量等因素的影响.结果表明,聚合反应速率随着反应温度的提高而加快.随着引发剂和乳化剂用量的增加,乳液的粒径减小,乳液更加稳定.硅改性后的聚合物具有较好的耐水性和热稳定性.

  4. Natural Rubber Latex Modified by Nano SiO2 to Prepare Medical Gloves%用纳米SiO2改性胶乳制备新型医用橡胶手套

    Institute of Scientific and Technical Information of China (English)

    敖宁建

    2005-01-01

    Nano SiO2 modified natural rubber latex treated by ultrasonic and special dispersing agent was used to prepare medical gloves, and the mechanical and aging properties of the product were investigated. The results show that the tensile strength of the glove with 0.5% (mass fraction) nano SiO2 was 20.2MPa when the contrast was 15.9MPa. After 2% (mass fraction) nano SiO2 was filled in the latex, the tensile strength of the product increased to 25.5MPa. With the increase of the nano SiO2 content, strength at 300% and 500% elongation of the products increased gradually. Addition of nano SiO2 particles didn't change the elongation at break and elasticity of the glove. After 33 hours aging in hot air at 100℃, the tensile strength of the glove with 2% (mass fraction) nano SiO2 was as high as 12.7MPa.

  5. Latex and friends

    CERN Document Server

    Dongen, M R C van

    2012-01-01

    LaTeX is a free, automated state-of-the-art typesetting system. This book teaches all the ins and outs of LaTeX which are needed to write an article, report, thesis, or book. The book teaches by example, giving many worked out examples showing input and output side by side. The book presents the most recent techniques for presenting data plots, complex graphics, and computer presentations, but does not require previous knowledge. However, it is also a reference for the more seasoned user, with pointers to modern techniques and packages. Recurring themes in the book are consistent and effective

  6. Polyether/Polyester Graft Copolymers

    Science.gov (United States)

    Bell, Vernon L., Jr.; Wakelyn, N.; Stoakley, D. M.; Proctor, K. M.

    1986-01-01

    Higher solvent resistance achieved along with lower melting temperature. New technique provides method of preparing copolymers with polypivalolactone segments grafted onto poly (2,6-dimethyl-phenylene oxide) backbone. Process makes strong materials with improved solvent resistance and crystalline, thermally-reversible crosslinks. Resulting graft copolymers easier to fabricate into useful articles, including thin films, sheets, fibers, foams, laminates, and moldings.

  7. Human fibrinogen monolayers on latex particles: role of ionic strength.

    Science.gov (United States)

    Bratek-Skicki, Anna; Żeliszewska, Paulina; Adamczyk, Zbigniew; Cieśla, Michał

    2013-03-19

    The adsorption of human serum fibrinogen on polystyrene latex particles was studied using the microelectrophoretic and concentration depletion methods. Measurements were carried out for pH 3.5 and an ionic strength range of 10(-3) to 0.15 M NaCl. The electrophoretic mobility of latex was determined as a function of the amount of adsorbed fibrinogen (surface concentration). A monotonic increase in the electrophoretic mobility (zeta potential) of the latex was observed, indicating a significant adsorption of fibrinogen on latex for all ionic strengths. No changes in the latex mobility were observed for prolonged time periods, suggesting the irreversibility of fibrinogen adsorption. The maximum coverage of fibrinogen on latex particles was precisely determined using the depletion method. The residual protein concentration after making contact with latex particles was determined by electrokinetic measurements and AFM imaging where the surface coverage of fibrinogen on mica was quantitatively determined. The maximum fibrinogen coverage increased monotonically with ionic strength from 1.8 mg m(-2) for 10(-3) M NaCl to 3.6 mg m(-2) for 0.15 M NaCl. The increase in the maximum coverage was interpreted in terms of the reduced electrostatic repulsion among adsorbed fibrinogen molecules. The experimental data agree with theoretical simulations made by assuming a 3D unoriented adsorption of fibrinogen. The stability of fibrinogen monolayers on latex was also determined in ionic strength cycling experiments. It was revealed that cyclic variations in NaCl concentration between 10(-3) and 0.15 M induced no changes in the latex electrophoretic mobility, suggesting that there were no irreversible molecule orientation changes in the monolayers. On the basis of these experimental data, a robust procedure of preparing fibrinogen monolayers on latex particles of well-controlled coverage was proposed.

  8. The effect of hydrophilic and hydrophobic block length on the rheology of amphiphilic diblock Polystyrene-b-Poly(sodium methacrylate) copolymers prepared by ATRP.

    Science.gov (United States)

    Raffa, Patrizio; Stuart, Marc C A; Broekhuis, Antonius A; Picchioni, Francesco

    2014-08-15

    Following our previous investigation on the effect of molecular architecture on the rheology of Polystyrene-b-Poly(sodium methacrylate) copolymers (PS-b-PMAA), we consider here diblock PS-b-PMAA copolymers characterized by a different length of either the hydrophilic or the hydrophobic block. Various copolymers characterized by different PS or PMAA block length have been prepared by ATRP (kinetics is also discussed) and studied from the point of view of their rheological behaviour in water. To the best of our knowledge, this is the first systematic investigation concerning the effect of block length on the rheology of diblock polyelectrolytes. We found that the hydrophobic block length has small influence on the rheology. Surprisingly, the polymers with shortest PMAA blocks yield the strongest gels at high concentration. A simple model based on the classical theories of self-assembly and percolation of amphiphilic polymers has been here developed in order to explain the observed data. Copyright © 2014 Elsevier Inc. All rights reserved.

  9. The Influence of Comonomer on Ethylene/α-Olefin Copolymers Prepared Using [Bis(N-(3-tert butylsalicylideneanilinato] Titanium (IV Dichloride Complex

    Directory of Open Access Journals (Sweden)

    Patcharaporn Kaivalchatchawal

    2011-02-01

    Full Text Available We describe the synthesis of [bis(N-(3-tert-butylsalicylideneanilinato] titanium (IV dichloride (Ti-FI complex and examine the effects of comonomer (feed concentration and type on its catalytic performance and properties of the resulting polymers. Ethylene/1-hexene and ethylene/1-octene copolymers were prepared through copolymerization using Ti-FI catalyst, activated by MAO cocatalyst at 323 K and 50 psi ethylene pressure at various initial comonomer concentrations. The obtained copolymers were characterized by DSC, GPC and 13C-NMR. The results indicate that Ti-FI complex performs as a high potential catalyst, as evidenced by high activity and high molecular weight and uniform molecular weight distribution of its products. Nevertheless, the bulky structure of FI catalyst seems to hinder the insertion of α-olefin comonomer, contributing to the pretty low comonomer incorporation into the polymer chain. The catalytic activity was enhanced with the comonomer feed concentration, but the molecular weight and melting temperature decreased. By comparison both sets of catalytic systems, namely ethylene/1-hexene and ethylene/1-octene copolymerization, the first one afforded better activity by reason of easier insertion of short chain comonomer. Although 1-hexene copolymers also exhibited higher molecular weight than 1-octene, no significant difference in both melting temperature and crystallinity can be noticed between these comonomers.

  10. Latex allergy in health care

    Directory of Open Access Journals (Sweden)

    Tina Virtič

    2012-11-01

    Full Text Available The increasing use of natural rubber latex medical gloves in the last three decades has caused an increase in latex allergy. The majority of risk groups for allergy development include health care workers, workers in the rubber industry, atopic individuals and children with congenital malformations. Three types of pathological reactions can occur in people using latex medical gloves: irritant contact dermatitis, allergic contact dermatitis and immediate hypersensitivity. The latex allergy is caused by constituent components of latex gloves and added powders; there are also numerous latex allergens involved in cross-reactivity between latex and fruits and vegetables, the so-called latex-fruit syndrome. The diagnosis is based on an accurate history of exposure, clinical presentation and confirmatory in vivo and in vitro tests. Prevention is the easiest, most effective and least expensive way to avoid latex allergy. Powder-free latex gloves with reduced levels of proteins and chemicals, and synthetic gloves for allergic workers must be provided in the work environment. There are already many health care institutions around the world where all latex products have been replaced by synthetic material products.

  11. Preparation and in vitro evaluation of doxorubicin-loaded Fe3O4 magnetic nanoparticles modified with biocompatible copolymers

    Directory of Open Access Journals (Sweden)

    Akbarzadeh A

    2012-02-01

    Full Text Available Abolfazl Akbarzadeh1, Haleh Mikaeili2, Nosratollah Zarghami3, Rahmati Mohammad3, Amin Barkhordari3, Soodabeh Davaran21Drug Applied Research Center, 2Tuberculosis and Lung Disease Research Center of Tabriz, 3Department of Clinical Biochemistry and Laboratory Medicine, Division of Medical Biotechnology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, IranBackground: Superparamagnetic iron oxide nanoparticles are attractive materials that have been widely used in medicine for drug delivery, diagnostic imaging, and therapeutic applications. In our study, superparamagnetic iron oxide nanoparticles and the anticancer drug, doxorubicin hydrochloride, were encapsulated into poly (D, L-lactic-co-glycolic acid poly (ethylene glycol (PLGA-PEG nanoparticles for local treatment. The magnetic properties conferred by superparamagnetic iron oxide nanoparticles could help to maintain the nanoparticles in the joint with an external magnet.Methods: A series of PLGA:PEG triblock copolymers were synthesized by ring-opening polymerization of D, L-lactide and glycolide with different molecular weights of polyethylene glycol (PEG2000, PEG3000, and PEG4000 as an initiator. The bulk properties of these copolymers were characterized using 1H nuclear magnetic resonance spectroscopy, gel permeation chromatography, Fourier transform infrared spectroscopy, and differential scanning calorimetry. In addition, the resulting particles were characterized by x-ray powder diffraction, scanning electron microscopy, and vibrating sample magnetometry.Results: The doxorubicin encapsulation amount was reduced for PLGA:PEG2000 and PLGA:PEG3000 triblock copolymers, but increased to a great extent for PLGA:PEG4000 triblock copolymer. This is due to the increased water uptake capacity of the blended triblock copolymer, which encapsulated more doxorubicin molecules into a swollen copolymer matrix. The drug encapsulation efficiency achieved for Fe3O4 magnetic nanoparticles

  12. Preparation and Characterization of Polymeric Micelles from Poly(D,L-lactide) and Methoxypolyethylene Glycol Block Copolymers as Potential Drug Carriers

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Amphiphilic diblock copolymers composed of methoxy polyethylene glycol (MePEG) and poly(D,L-lactide) (PDLLA) were prepared for the preparation of polymeric micelles. The use of MePEG-PDLLA as drug carriers has been reported in the open literature, but there are only few data on the application of a series of MePEG-PDLLA copolymers with different lengths in the medical field. The shape of the polymeric micelles is also important in drug delivery. Studies on in vitro drug release profiles require a good sink condition. The critical micelle concentration of a series of MePEG-PDLLA has a significant role in drug release. To estimate their feasibility as a drug carrier, polymeric micelles made of MePEG-PDLLA block copolymer were prepared by the oil in water (O/W) emulsion method. From dynamic light scattering (DLS) measurements,the size of the micelle formed was less than 200 nm. The critical micelle concentration of polymeric micelles with various compositions was determined using pyrene as a fluorescence probe. The critical micelle concentration decreased with increasing number of hydrophobic segments. MePEG-PDLLA micelles have a considerably low critical micelle concentration (0.4-0.5 μg/mL), which is apparently an advantage in utilizing these micelles as drug carriers. The morphology of the polymeric micelles was observed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The micelles were found to be nearly spherical. The yield of the polymeric micelles obtained from the ONV method is as high as 85%.

  13. LATEX HYBRIDES URETHANE/ACRYLIQUE POUR APPLICATIONS ADHESIVES

    OpenAIRE

    Degrandi, Elise

    2009-01-01

    This work focuses on adhesive films obtained upon film formation of urethane/acrylic hybrid latex particles. These latexes were prepared by a miniemulsion polymerization to ensure a homogeneous incorporation of the PU inside the particles. Studying the morphology of particles and films showed that the grafting of polyurethane is essential to avoid phase separation at the film scale which is harmful for the macroscopic properties. Two parameters affect the mechanical properties of the films: t...

  14. Preparation of Pressure Sensitive Adhesives Based on Visible Light-Cured Natural Rubber Latex%可见光固化天然胶乳压敏胶的研制

    Institute of Scientific and Technical Information of China (English)

    唐盛斌; 徐志义; 廖建和; 陈永平; 廖双泉; 桂红星

    2009-01-01

    Degraded natural latex was mixed with terpene resin emulsion and other additives and then cured under the visible light initiator system to prepare oil-in-water emulsion type of pressure-sensitive adhesive (PSA). The ratio of degraded natural rubber to terpene resin emulsion,molecular weight and amounts of other additives were measured to observe their effects on the properties of PSA under a given light intensity. The results showed that the PSA with optimum properties was prepared under the following conditions: the ratio of the degraded natural latex and terpene resin emulsion was 1:1,molecular weight of the degraded natural rubber latex 19.8×10~4,the amount of initiator 1.2%,the amount of cross-linker 15%,and the amount of accelerant 0.4%. The DSC and TG/DTG showed that the PSA was improved in thermal stability after the PSA containing photo-initiator was cured by visible light. The PSA containing photo-initiator showed an increase of 5℃ in Tg,and was still available under a very low temperature.%采用可见光引发体系固化将降解天然胶乳与萜烯树脂乳液的其他助剂组合制备水乳型压敏胶,研究在一定光照强度下,降解天然胶乳与萜烯树脂乳液的不同配比,天然胶乳不同分子量,其他助剂的用量对压敏胶性能的影响.结果表明,降解天然胶乳与萜烯树脂乳液质量比为1:1、降解天然胶乳分子量为19.8×10~4、引发剂1.2%、交联剂15%、促进剂0.4%时压敏胶性能最优.DSC和TG/DTG表明含有光引发剂的压敏胶在光照后热稳定性提高,压敏胶的Tg升高了5℃,仍具有很低的使用温度.

  15. The preparation of PLL-GRGDS modified PTSG copolymer scaffolds and their effects on manufacturing artificial salivary gland.

    Science.gov (United States)

    Zhu, Jie; Zhang, Yueming; Xu, Nanwei; Wang, Liqun; Xiang, Xu; Zhu, Xiaolin

    2013-01-01

    We prepared two-dimentional (2D) and three-dimentional (3D) scaffolds with biodegradable poly(butylene terephthalate)-co-poly(butylene succinate)-b-poly(ethylene glycol) (i.e. PTSG), mainly for the purpose of investigating its cytocompatibility and mechanical property as artificial salivary gland material. The surface of 2D scaffold (i.e. PTSG film) was modified by O(2) plasma treatment and the following coating of Gly-Arg-Gly-Asp-Ser (GRGDS) decorated poly(L-lysine) (i.e. PLL-GRGDS). The obtained film was named PLL-GRGDS/PTSG (O). Its surface properties were characterized using contact angles, surface energies, X-ray photoelectron spectroscopy and Fourier transform infrared; and cytocompatibility tests in vitro including morphology, attachment and proliferation of human salivary gland (HSG) epithelial cells were further performed on PTSG films. Meanwhile, 3D scaffold with the shape of porous tube was constructed using hydrogel-rapid prototyping and the performance of 3D scaffold including mechanical property, pore structure, degradation and water uptake was also evaluated. Results revealed that PLL-GRGDS/PTSG (O) possessed the high surface free energy (63.89 mJ/m(2)) and could immobilize a great amount of PLL-GRGDS, which attributed to the formation of some polar oxygen-containing groups such as carboxyl and carbonyl ones in the process of O(2) plasma treatment. Cell tests in vitro suggested the efficiency of surface modification in enhancing the cytocompatibility of PTSG. Furthermore, the manufacturing scaffold was proved to possess excellent pore structures (porosity 88.9%, connectivity 97.5% and average pore size 35.4 μm) and good mechanical properties (E-modulus 88.4 ± 4.1 kPa, yield stress 45.7 ± 2.3 kPa, yield strain 56 ± 2%, fracture stress 52.2 ± 3.5 kPa and fracture strain 63 ± 3%). After four weeks hydrolysis reaction, the degradation of the scaffold reached 8% and equilibrium water uptake declined from 51 to 45%. The

  16. Preparation of starch-poly-glutamic acid graft copolymers by microwave irradiation and the characterization of their properties

    Science.gov (United States)

    Graft copolymers of waxy maize starch and poly-y-glutamic acid (PGA) were produced in an aqueous solution using microwave irradiation. The microwave reaction conditions were optimized with regard to temperature and pH. The temperature of 180 deg C and pH 7.0 were the best reaction conditions resulti...

  17. Effect of cationic monomer on properties of fluorinated acrylate latex

    Institute of Scientific and Technical Information of China (English)

    Li Jun Chen

    2012-01-01

    Cationic fluorinated acrylate latex was prepared via semi-continuous emulsion copolymerization of cationic monomer and other monomers.The resultant latex and its film were characterized with dynamic light scattering detector and contact angle meter.Influences of amount of DMDAAC on the properties of resultant latex and its film were investigated in detail.Results show that the particle size of the latex has the minimum value and the zeta potential of the latex is increased when the amount of DMDAAC is increased.In addition,the particle size of the latex is unimodal distribution when the amount of DMDAAC is not more than 2.5%.However,the particle size of the latex is bimodal distribution when the amount of DMDAAC is more than 2.5%.The contact angle is varied slightly with the increase of amount of DMDAAC when it is not more than 2.5%.Nevertheless,the contact angle is decreased with the increase of the amount of DMDAAC when it is more than 25%.

  18. Graft Copolymerization of Methyl Methacrylate Monomer onto Starch and Natural Rubber Latex Initiated by Gamma Irradiation

    Directory of Open Access Journals (Sweden)

    S. Iskandar

    2011-04-01

    Full Text Available To obtain the degradable plastic, the graft copolymerization of methyl methacrylate onto starch and natural rubber latex was conducted by a simultaneous irradiation technique. Gamma-ray from cobalt-60 source was used as the initiator. The grafted copolymer of starch-polymethyl methacrylate and the grafted copolymer of natural rubber-polymethyl methacrylate were mixed in the blender, and dried it in the oven. The dried grafted copolymer mixture was then molded using hydraulic press machine. The effect of irradiation dose, composition of the grafted copolymer mixture, film forming condition and recycle effect was evaluated. The parameters observed were tensile strength, gel fraction and soil burial degradability of grafted copolymer mixture. It was found that the tensile strength of grafted copolymer mixture increased by -ray irradiation. Increasing of the grafted copolymer of natural rubber-polymethyl methacrylate content, the gel fraction and tensile strength of the grafted copolymer mixture increased. The tensile strength of the grafted copolymer mixture was increased from 18 MPa to 23 MPa after recycled (film forming reprocessed 3 times. The grafted copolymer mixture was degraded completely after soil buried for 6 months

  19. 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 w

  20. Carboxylic-containing copolymer as template to prepare CdS, ZnS and doped nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    CdS, CdS:Mn, ZnS, ZnS:Mn and ZnS:Tb nanoparticles were preparedby using carboxylic-containing copolymer, polystyrene-maleic anhydride (PSM), as template. Average particle size, 2.5 nm for CdS nanoparticles, is deduced from UV-vis absorption spectra and consistent with the observation of TEM. Characteristic emissions of the doping ions can be observed and the energy transfer from the host to the doping ions is verified. Fourier transform infrared (FTIR) spectra were studied to confirm the bonding effect of the copolymer and the metal ions. PSM hydrolyzed and chelated metal ions by its carboxylic group, and then performed as a protection layer after the formation of nanoparticles.

  1. Preparation and Mechanical Properties of Solid-phase Grafting Nanocomposites of PVC/Graft Copolymers/MMT

    Institute of Scientific and Technical Information of China (English)

    ZHOU Dunbai; CAI Changgen; JIA Demin

    2006-01-01

    In order to improve the mechanical properties of PVC, by solid-phase grafting reaction, grafting on and nano-modifying the PVC process synchronously, acrylic monomers not only graft on PVC, but also are intercalated into the layers of MMT in the heating process. Blending PVC and the MMT-PVC grafting copolymers, we can get nanocomposites of PVC/ grafters/ MMT, and the mechanical performance of the material is improved.

  2. A poly(ether-ester) copolymer for the preparation of nanocarriers with improved degradation and drug delivery kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Gagliardi, M., E-mail: mariacristina.gagliardi@iit.it [Center for Micro Bio-Robotics @SSSA, Istituto Italiano di Tecnologia, Viale Rinaldo Piaggio 34, 56025 Pontedera (Italy); Bertero, A. [Department of Biology, Unit of Cellular and Developmental Biology, University of Pisa, S.S.12 Abetone e Brennero 4, 56127 Pisa (Italy); Center for Neuroscience and Cognitive Systems @UNITN, Istituto Italiano di Tecnologia, Corso Bettini 31, 38068 Rovereto (Italy); Bardi, G. [Center for Bio-Molecular Nanotechnologies @UniLe, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Italy); Bifone, A. [Center for Neuroscience and Cognitive Systems @UNITN, Istituto Italiano di Tecnologia, Corso Bettini 31, 38068 Rovereto (Italy)

    2016-02-01

    This paper reports the synthesis and the physicochemical, functional and biological characterisations of nanocarriers made of a novel di-block biodegradable poly(ether-ester) copolymer. This material presents tunable, fast biodegradation rates, but its products are less acidic than those of other biosorbable polymers like PLGA, thus presenting a better biocompatibility profile and the possibility to carry pH-sensitive payloads. A method for the production of monodisperse and spherical nanoparticles is proposed; drug delivery kinetics and blood protein adsorption were measured to evaluate the functional properties of these nanoparticles as drug carriers. The copolymer was labelled with a fluorescent dye for internalisation tests, and rhodamine B was used as a model cargo to study transport and release inside cultured cells. Biological tests demonstrated good cytocompatibility, significant cell internalisation and the possibility to vehiculate non-cell penetrating moieties into endothelial cells. Taken together, these results support the potential use of this nanoparticulate system for systemic administration of drugs. - Highlights: • We propose a novel biodegradable nanocarrier for intracellular drug delivery. • Biodegradation rates can be finely tuned by controlling copolymer composition. • Degradation products are less acidic, thus enabling delivery of pH-sensitive cargoes. • We demonstrate intracellular delivery of a non-cell-penetrating model drug. • No significant membrane damage by the polymer nanocarriers is observed.

  3. Study on the preparation of soap-free styrene-acrylic latex%无皂苯丙乳液的制备工艺研究

    Institute of Scientific and Technical Information of China (English)

    丁长波; 赵振河; 杨少艳

    2015-01-01

    通过将反应型乳化剂DNS-86与DNS-1035复配,引入交联单体丙烯酸羟乙酯(HEA),合成了一系列性能优异的无皂苯丙乳液粘合剂。结果表明:固含量为(45±2)%,单体转化率较高,乳液凝胶率较小,且乳液离心稳定性、储存稳定性、稀释稳定性、电解质(Ca2+)稳定性和酸碱稳定性均良好;采用无皂苯丙乳液印花的织物耐干、湿摩擦色牢度和耐皂洗色牢度等级与市售涂料印花粘合剂相当;红外光谱(FT-IR)分析表明:优化后的苯丙乳液中没有C C双键存在,即没有反应型乳化剂的剩余,实现了无皂乳液聚合。—%A series of soap- free styrene- acrylic latex with excel ent performance were synthesized through the compound of reactive emulsifier DNS- 86 and DNS- 1035 and the introduction of cross- linking monomer hydroxyethyl acrylate (HEA). The results showed that solids content was (45 ± 2)%, the monomer conversion rate was higher, and the emulsion coagulation rate was lower. In addition, the emulsion centrifugal stability, storage stability, dilution stability, electrolytes (Ca2+) stability, and pH stability were good. The dry and wet rubbing fastness and soaping fastness of soap- free styrene- acrylic latex printed fabric were similar with those of pigment printing binder on market. Final y, infrared spectrum (FT- IR) analysis indicated that C C functional group did not existed in the optimized styrene and butyl- acrylic emulsion, namely there was no re⁃maining reactive emulsifier. Thus soap- free emulsion polymerization was realized.

  4. Verapamil hydrochloride release characteristics from new copolymer zwitterionic matrix tablets.

    Science.gov (United States)

    Kostova, Bistra; Kamenska, Elena; Ivanov, Ivo; Momekov, George; Rachev, Dimitar; Georgiev, George

    2008-01-01

    The aim of this study was to synthesize stable copolymer (vinyl acetate-co-3-dimethyl[methacryloyloxyethyl] ammonium propane sulfinate) zwitterionic latex with different compositions for the first time by emulsifier-free emulsion copolymerization. Throughout the course of the study, a proposal was made for the explanation of the relationship between the "overshooting" phenomenon (a swelling kinetics with a maximum) and the specific self-association of the zwitterionic copolymers. The zwitterionic monomer unit mole fraction, pH, and ionic strength effects on this relationship, on the swelling kinetics of the zwitterionic copolymers, and on the sustained verapamil hydrochloride release from the model tablets were established by the study's authors.

  5. Self-assembled PEG-b-PDPA-b-PGEM copolymer nanoparticles as protein antigen delivery vehicles to dendritic cells: preparation, characterization and cellular uptake

    Science.gov (United States)

    Li, Pan; Zhou, Junhui; Huang, Pingsheng; Zhang, Chuangnian; Wang, Weiwei; Li, Chen; Kong, Deling

    2017-01-01

    Antigen uptake by dendritic cells (DCs) is a key step for initiating antigen-specific T cell immunity. In the present study, novel synthetic polymeric nanoparticles were prepared as antigen delivery vehicles to improve the antigen uptake by DCs. Well-defined cationic and acid-responsive copolymers, monomethoxy poly(ethylene glycol)-block-poly(2-(diisopropyl amino) ethyl methacrylate)-block-poly(2-(guanidyl) ethyl methacrylate) (mPEG-b-PDPA-b-PGEM, PEDG) were synthesized by reversible addition-fragmentation chain transfer polymerization of 2-(diisopropylamino)ethyl methacrylate) and N-(tert-butoxycarbonyl) amino ethyl methacrylate monomers, followed by deprotection of tert-butyl protective groups and guanidinylation of obtained primary amines. 1H NMR, 13C NMR and GPC results indicated the successful synthesis of well-defined PEDG copolymers. PEDG copolymers could self-assemble into nanoparticles in aqueous solution, which were of cationic surface charges and showed acid-triggered disassembly contributed by PGEM and PDPA moieties, respectively. Significantly, PEDG nanoparticles could effectively condense with negatively charged model antigen ovalbumin (OVA) to form OVA/PEDG nanoparticle formulations with no influence on its secondary and tertiary structures demonstrating by far-UV circular dichroism and UV–vis spectra. In vitro antigen cellular uptake by bone marrow DCs (BMDCs) indicated using PEDG nanoparticles as antigen delivery vehicles could significantly improve the antigen uptake efficiency of OVA compared with free OVA or the commercialized Alum adjuvant. Moreover, as the surface cationic charges of OVA/PEDG nanoparticle formulations reduced, the uptake efficiency decreased correspondingly. Collectively, our work suggests that guanidinylated, cationic and acid-responsive PEDG nanoparticles represent a new kind of promising antigen delivery vehicle to DCs and hold great potential to serve as immunoadjuvants in the development of vaccines. PMID:28149525

  6. Performance Analysis of Styrene Butadiene Rubber-Latex on Cement Concrete Mixes.

    Directory of Open Access Journals (Sweden)

    Er. Kapil Soni

    2014-03-01

    Full Text Available To improve the performance of concrete, polymers are mixed with concrete. It has been observed that polymer-modified concrete (PMC is more durable than conventional concrete due to superior strength and high durability. In this research, effect of Styrene-Butadiene Rubber (SBR latex on compressive strength and flexural strength of concrete has been studied and also the optimum polymer (SBR-Latex content for concrete is calculated. This research was carried out to establish the effects of polymer addition on compressive and flexural strength using concrete with mix design of constant water-cement ratio at local ambient temperature. The mixes were prepared with Styrene-Butadiene Rubber (SBR latex -cement ratio of 0 %, 5%, 10%, 15% and 20%. Slump test was conducted on fresh concrete while compressive strength and flexural strength were determined at different age. A locally available Perma-Latex is used as SBR Latex. It has been observed that SBR latex has negative effect at early age while at 28 days, the addition of SBR latex in concrete results in enhancement of compressive strength and Flexural Strength. Based on the results of this study, latex modified concrete made using Perma-Latex may be recommended to be used with various types of concrete structures. However, for the mixes rich in cement, the dosage of SBR latex needs to be adjusted to maintain required workability of concrete.

  7. Proteomic analysis of latex from the rubber-producing plant Taraxacum brevicorniculatum.

    Science.gov (United States)

    Wahler, Daniela; Colby, Thomas; Kowalski, Natalie A; Harzen, Anne; Wotzka, Sandra Y; Hillebrand, Andrea; Fischer, Rainer; Helsper, Johannes; Schmidt, Jürgen; Schulze Gronover, Christian; Prüfer, Dirk

    2012-03-01

    Many plants produce latex, a specialized, metabolically active cytoplasm. This is generally regarded as a defensive trait but latex may also possess additional functions. We investigated the role of latex in the dandelion species Taraxacum brevicorniculatum that contains considerable amounts of high-quality natural rubber by carrying out a comprehensive analysis of the latex proteome. We developed reliable protocols for the preparation of protein samples for one-dimensional gel electrophoresis, two-dimensional gel electrophoresis, and subsequent mass spectrometry analysis, which led to 278 unique identifications. A gene ontology classification system based on comparisons with known Arabidopsis thaliana root proteins showed that dandelion proteins involved in lipid metabolism and transport were enriched in the latex proteome, whereas those involved in stress responses were not. We also found that proteins involved in rubber biosynthesis were distributed among different fractions of the latex proteome.

  8. Latex Allergy: A Prevention Guide

    Science.gov (United States)

    ... in some gloves. When workers change gloves, the protein/powder particles become airborne and can be inhaled. How ... infectious materials. If you choose latex gloves, use powder-free gloves with reduced protein content. Such gloves reduce exposures to latex protein ...

  9. Capsular Serotyping of Streptococcus pneumoniae by latex agglutination.

    Science.gov (United States)

    Porter, Barbara D; Ortika, Belinda D; Satzke, Catherine

    2014-09-25

    Latex agglutination reagents are widely used in microbial diagnosis, identification and serotyping. Streptococcus pneumoniae (the pneumococcus) is a major cause of morbidity and mortality world-wide. Current vaccines target the pneumococcal capsule, and there are over 90 capsular serotypes. Serotyping pneumococcal isolates is therefore important for assessing the impact of vaccination programs and for epidemiological purposes. The World Health Organization has recommended latex agglutination as an alternative method to the 'gold standard' Quellung test for serotyping pneumococci. Latex agglutination is a relatively simple, quick and inexpensive method; and is therefore suitable for resource-poor settings as well as laboratories with high-volume workloads. Latex agglutination reagents can be prepared in-house utilizing commercially-sourced antibodies that are passively attached to latex particles. This manuscript describes a method of production and quality control of latex agglutination reagents, and details a sequential testing approach which is time- and cost-effective. This method of production and quality control may also be suitable for other testing purposes.

  10. Latex allergy in clinical practice

    Directory of Open Access Journals (Sweden)

    R Pradeep Kumar

    2012-01-01

    Full Text Available A continuous exposure or contact to latex products may sensitize the human body by causing mild to fatal reactions. Despite the availability of the literature, medical personnel are still unaware of the implications of the use of latex materials. The increased awareness to prevent the transmission of infectious blood borne pathogens has lead to increased usage of medical gloves among health care workers. This increased usage of medical gloves, along with improved methods in diagnosing latex allergy, has been the reason for the rise in the number of reported cases. This has lead to recognition of latex allergy as a serious medical concern. Patients in high-risk groups must be assessed carefully, so that appropriate protocols can be used to protect them from contact with latex.

  11. Synthesis and characterization of Zwitterionic co-polymers as matrices for sustained metoprolol tartrate delivery.

    Science.gov (United States)

    Kamenska, Elena; Kostova, Bistra; Ivanov, Ivo; Rachev, Dimitar; Georgiev, George

    2009-01-01

    Very stable co-polymer (vinyl acetate (VA)-co-3-dimethyl(methacryloyloxyethyl) ammonium propane sulfonate (DMAPS) (p(VA-co-DMAPS)) latexes with different compositions have been synthesized by emulsifier-free emulsion co-polymerization. The dry p(VA-co-DMAPS)s have been used in the preparation of drug tablets for sustained Metoprolol tartrate release. It has been shown that the tablet swelling depends on the mol fraction of DMAPS monomer units (m(DMAPS)), pH and ionic strength (I). An original explanation, based on the swelling behavior of p(VA-co-DMAPS), has been proposed for the "overshooting" phenomenon observed. It assumes the formation of hydrophilic domains with a higher m(DMAPS) in the co-polymer tablets. The formation of dipole-dipole clusters between the DMAPS units at different m(DMAPS) and I are the main cause for the established differences in both the swelling kinetics of the p(VA-co-DMAPS) matrices and Metoprolol tartrate release. The obtained results show that for p(VA-co-DMAPS) matrices-based tablets controlled sustained Metoprolol tartrate release can be realized just by varying two parameters, co-polymer composition and I.

  12. Preparation of Organic Phosphate Modified Styrene-Acrylate Grafted Epoxy Resins Latex and Its Anti-Corrosion Property%磷酸酯改性苯丙接枝环氧树脂胶乳的制备及其防腐蚀性能

    Institute of Scientific and Technical Information of China (English)

    毛正和; 钟涛; 朱爱萍; 夏中高; 杨芳芳

    2012-01-01

    采用乳液聚合方法制备了一种用于水性金属防腐蚀涂料的磷酸酯改性苯丙接枝环氧树脂胶乳,其中环氧树脂占胶乳固体含量30%,磷酸酯占胶乳固体含量1.2%.制备的胶乳可室温交联固化.采用透射电镜表征了胶乳的形貌,红外光谱表征胶乳的结构,偏光显微镜研究金属的闪锈行为,拉开法测定附着力.结果表明:胶乳粒子呈现规则的球型形貌,粒径为130 ~ 150 nm,粒径分布均匀;磷酸酯以共价键的方式连接在苯丙接枝环氧树脂胶乳中;胶乳具有优异的防闪锈性,干/湿附着力优异,同时乳胶膜具有优异的机械力学性能、耐盐水性能以及防腐蚀性能.%Emulsion polymerization was used to prepare the organic phosphate modified styrene — acrylate grafted epoxy resins latex for preparation of the waterborne metal anticorrosive coatings, in which epoxy resin content was 30% and organic phosphate content was 1.2%. The resulting latex could be crosslinked at room temperature. The latex morphology was characterized with TEM; the structure was measured with FT - IR; the flash rust behaviors on metals were studied with the polarizing microscope; and the adhesion was measured with the pull - off method. The results indicated that the latex particles showed regular spheroidal morphology, with 130-150 nm in diameter and uniform particle size distribution; the organic phosphate linked with styrene - acrylate grafted epoxy resins latex by covalent bond; the latex was excellent in flash rust resistance and drying/wet adhesion. And the latex film could provide good mechanical properties, salt water resistance and anti - corrosion property.

  13. Preparation and characterization of a powder containing an oily liquid drug with Eudragit EPO or L100 copolymer.

    Science.gov (United States)

    Fujii, Makiko; Kawakami, Ayari; Saito, Asumi; Tuchiya, Haruna; Koizumi, Naoya; Watanabe, Yoshiteru

    2016-12-01

    Oily liquid drugs are not convenient for oral administration. We developed a powder containing clofibrate (CF), a model of an oily drug, using aminoalkyl methacrylate copolymer (EPO) or methacrylic acid copolymer (L100). CF or a mixture of CF and soybean oil was emulsified with EPO or L100 aqueous solution. Using a high-pressure homogenizer, a stable emulsion was obtained, and a powder was then obtained by lyophilization of the emulsion. The content of CF in the powder depended on the formulation, with the highest contents being 24.6% and 27.1% for EPO and L100, respectively. The incorporation ratio of CF was higher for L100 than for EPO. The powder using EPO was sticky because of leaked CF and the low glass transition temperature of EPO. The powder using L100 was a typical powder obtained by lyophilization. The leakage of CF from the powder was EPO powder. The dissolution of CF from powder using EPO was fast, regardless of the pH of the medium, but the powder using L100 showed enteric-soluble characteristics, indicating that CF is well incorporated in L100.

  14. ABA TRIBLOCK COPOLYMERS WITH PENDANT HYDROXYL GROUPS PREPARED BY CONTROLLED CATIONIC POLYMERIZATION AND THEIR USE AS DELIVERY CARRIER FOR PACLITAXEL

    Institute of Scientific and Technical Information of China (English)

    Ping Ren; Yi-bo Wu; Wen-li Guo; Shu-xin Li; Ying Chen

    2013-01-01

    To improve the hydrophilicity of poly(styrene-b-isobutylene-b-styrene) (SIBS),this study focuses on the synthesis of novel functional ABA triblock copolymer thermoplastic elastomers (TPEs) with polyisobutylene (PIB) as rubbery segments.The precursor poly{(styrene-co-4-[2-(tert-butyldimethylsiloxy) ethyl]styrene)-b-isobutylene-b-(styrene-co-4-[2-(tert-butyldimethylsiloxy)ethyl]styrene)}(P(St-co-TBDMES)-PIB-P(St-co-TBDMES)) triblock copolymer was first synthesized by living sequential cationic copolymerization of isobutylene (IB) with styrene (St) and 4-[2-(tert-butyldimethylsiloxy)ethyl]styrene (TBDMES) using 1,4-di(2-chloro-2-propyl)benzene (DiCumC1)/titanium tetrachloride (TiCl4)/2,6-di-tert-butylpyridine (DtBP) as the initiating system.Then,P(St-co-TBDMES)-PIB-P(St-co-TBDMES) was hydrolyzed in the presence of tetra-butylammonium fluoride to yield poly{[styrene-co-4-(2-hydroxyethyl)styrene]-b-isobutylene-b-[styrene-co-4-(2-hydroxyethyl)styrene]} (P(St-co-HOES)-PIB-P(St-co-HOES)) with pendant hydroxyl groups.P(St-co-HOES)-PIB-P(St-co-HOES) used as the paclitaxel carrier was also investigated in this study.Comparing with SIBS,P(St-co-HOES)-PIB-P(St-co-HOES) has exhibited better compatibility with paclitaxel and higher release rate.

  15. Preparation and solution behavior of a thermoresponsive diblock copolymer of poly(ethyl glycidyl ether) and poly(ethylene oxide).

    Science.gov (United States)

    Ogura, Michihiro; Tokuda, Hiroyuki; Imabayashi, Shin-ichiro; Watanabe, Masayoshi

    2007-08-28

    A thermoresponsive diblock copolymer, poly(ethyl glycidyl ether)-block-poly(ethylene oxide) (PEGE-b-PEO), is synthesized by successive anionic ring-opening polymerization of ethyl glycidyl ether and ethylene oxide using 2-phenoxyethanol as a starting material, and its solution behavior is elucidated in water. In a dilute 1 wt % solution, the temperature-dependent alteration in the polymer hydrodynamic radius (RH) is measured in the temperature range between 5 and 45 degrees C by pulse-gradient spin-echo NMR and dynamic light scattering. The RH value increased with temperature in two steps, where the first step at 15 degrees C corresponds to the core-shell micelle formation and the second step at 40 degrees C corresponds to the aggregation of the core-shell micelles. The formation of the core-shell micelles is supported by the solubilization of a dye (1,6-diphenyl-1,3,5-hexatriene) in the hydrophobic core, which is recognized for a copolymer solution in the temperature range between 20 and 40 degrees C. In this temperature range, the core-shell micelles and the unimers coexist and the fraction of the former gradually increases with increasing temperature, suggesting equilibrium between the micelles and the unimers. In the concentrated regime (40 wt % solution), the solution forms a gel and the small-angle X-ray scattering measurements reveal the successive formation of hexagonal and lamellar liquid crystal phases with increasing temperature.

  16. 含聚二甲基硅氧烷的嵌段共聚物的制备技术%Preparation Technology of PDMS Containing Block Copolymers

    Institute of Scientific and Technical Information of China (English)

    关成梅; 罗正鸿

    2009-01-01

    The relevant preparation technology of PDMS containing block copolymers classified by polymerization mechanism was reviewed,which included anionic polymerization,poly-condensation,free radical polymerization,atom transfer radical polymerization,and reversible addition-fragmentation chain transfer polymerization.%按聚合机理划分方法综述了含聚二甲基硅氧烷的嵌段共聚物的相关制备技术.包括阴离子聚合法、缩聚法、氧氮自由基聚合法、原子转移自由基聚合法、可逆加成-断裂链转移聚合法.

  17. Study on preparing gelatin graft copolymer emulsion as sizing agent%明胶接枝共聚物乳液施胶剂的研制

    Institute of Scientific and Technical Information of China (English)

    张光华; 刘丽娟; 王帆

    2011-01-01

    With acrylic acid(AA) as functional monomer,styrene(St) as hard monomer.butyl acrylate(BA)as soft monomer and polyvinyl alcohol ( PVA ) as protective agent and dispering agent, a gelatin graft copolymer(gelatin-g-copolymer) emulsion with core/shell structre as sizing agent was prepared by soap-free seeded emulsion polymerization,according to cation characteristic of gelatin in acidic solution. The optimal process conditions of preparing sizing agent were preferred by single factor experiment method ,and the physicochemical properties and application properties of the sizing agent were investigated. The results showed that the application properties of sizing paper.which was treated by the gelatin-g-copolymer emulsion,were nearer or more than those by the import congeneric product,the water resistance of sizing paper was better than that of raw paper because the water contact angles of the former and the latter were 104° and 73° respectively when mass ratio of m(gelatin):m(AA):m(St):m(BA):m(PVA) was 3:0.5:6:4:0.25.and mass fraction of initiator was 5% and reaction temperature was 85 ℃.%以丙烯酸(AA)为功能单体、苯乙烯(St)为硬单体、丙烯酸丁酯(BA)为软单体、聚乙烯醇(PVA)为保护剂和分散剂,根据明胶在酸性溶液中呈阳离子的特点,采用无皂种子乳液聚合法制备核/壳型明胶接枝共聚物乳液施胶剂.采用单因素试验法优选制备施胶剂的最佳工艺条件,并对施胶剂的理化性能和应用性能进行了研究.结果表明:当m(明胶):m(AA):m(St):m(BA):m(PVA)=3:0.5:6:4:0.25、w(引发剂)=5%和反应温度为85℃时,明胶接枝共聚物乳液施胶纸的应用性能接近甚至超过进口同类产品,其耐水性明显优于原纸(两者水接触角分别为104°、73°).

  18. [Latex allergy--Part I].

    Science.gov (United States)

    Chełmińska, Marta

    2004-01-01

    Natural rubber latex (NRL), is a resin sap produced in the cells of caoutchouc plants. It is a water dispersion of cis-1,4-polisopren (caoutchouc)--35%, stabilized with little amounts of proteins, sugar, alcohol, fatty acids and salts. The concentration of all solid substances is about 40%, the rest is water. Immunogenicity of latex depends on the proteins it contains. For many years we read in medical papers about the cases of contact urticaria, asthma, rhinitis, and anaphylaxis after contacting with latex products. It turns out that medical staff is the group of high occupational risk, because of exposure to gloves and other latex products. It is connected with the fact of high gloves usage caused by the danger of virus infections: HIV, HBV, HCV. Latex allergy is one of the reasons of dramatic complications after surgical operations. People who are allergic to latex may have cross reactions to allergens not connected with occupational environment. These are: food and houseplants (Ficus benjamina). The frequency of latex allergy is about 0.1% of the population. In the groups of high risk the frequency rises sharply. It is 17% among medical staff and it reaches 60% among children with spina bifida.

  19. Radiation Vulcanised Natural Rubber Latex: safer than conventionally processed latex?

    NARCIS (Netherlands)

    Geertsma RE; Orzechowski TJH; Jonker M; Dorpema JW; Asten JAAM van; LGM

    1996-01-01

    Door middel van cytotoxiciteitstesten is aangetoond dat RVNRL (straling-gevulcaniseerde natuurlijke latex rubber) materialen aanzienlijk minder cytotoxisch zijn dan zwavel-gevulcaniseerde materialen. Dit is een sterke aanwijzing dat een deel van de allergieproblemen, namelijk de zogeheten Type

  20. Enhanced protein adsorption and patterning on nanostructured latex-coated paper.

    Science.gov (United States)

    Juvonen, Helka; Määttänen, Anni; Ihalainen, Petri; Viitala, Tapani; Sarfraz, Jawad; Peltonen, Jouko

    2014-06-01

    Specific interactions of extracellular matrix proteins with cells and their adhesion to the substrate are important for cell growth. A nanopatterned latex-coated paper substrate previously shown to be an excellent substrate for cell adhesion and 2D growth was studied for directed immobilization of proteins. The nanostructured latex surface was formed by short-wavelength IR irradiation of a two-component latex coating consisting of a hydrophilic film-forming styrene butadiene acrylonitrile copolymer and hydrophobic polystyrene particles. The hydrophobic regions of the IR-treated latex coating showed strong adhesion of bovine serum albumin (cell repelling protein), fibronectin (cell adhesive protein) and streptavidin. Opposite to the IR-treated surface, fibronectin and streptavidin had a poor affinity toward the untreated pristine latex coating. Detailed characterization of the physicochemical surface properties of the latex-coated substrates revealed that the observed differences in protein affinity were mainly due to the presence or absence of the protein repelling polar and charged surface groups. The protein adsorption was assisted by hydrophobic (dehydration) interactions.

  1. 40 CFR 428.100 - Applicability; description of the latex-dipped, latex-extruded, and latex-molded rubber subcategory.

    Science.gov (United States)

    2010-07-01

    ... latex-dipped, latex-extruded, and latex-molded rubber subcategory. 428.100 Section 428.100 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS RUBBER MANUFACTURING POINT SOURCE CATEGORY Latex-Dipped, Latex-Extruded, and Latex-Molded Rubber Subcategory §...

  2. Nanocomposites of NR/SBR Blend Prepared by Latex Casting Method: Effects of Nano-TiO2 and Polystyrene-Encapsulated Nano-TiO2 on the Cure Characteristics, Physical Properties, and Morphology

    Directory of Open Access Journals (Sweden)

    Anyaporn Boonmahitthisud

    2017-01-01

    Full Text Available Nanocomposites of 80/20 (w/w natural rubber (NR/styrene butadiene rubber (SBR blend with four loadings of either nanosized titanium dioxide (nTiO2 or polystyrene-encapsulated nTiO2 (PS-nTiO2, ranging from 3 to 9 parts by weight per hundred of rubber (phr, were prepared by latex casting method. The PS-nTiO2 synthesized via in situ differential microemulsion polymerization displayed a core-shell morphology (nTiO2 core and PS shell with an average diameter of 42 nm. The cure characteristics (scorch time, cure time, and cure rate index, mechanical properties (tensile properties, tear strength, and hardness, thermal stability, glass transition temperature, and morphology of the prepared nanocomposites were quantified and compared. The results showed that the cure characteristics of all the nanocomposites were not significantly changed compared to those of the neat NR/SBR blend. The inclusion of an appropriate amount of either nTiO2 or PS-nTiO2 into the NR/SBR blend apparently improved the tensile strength, modulus at 300% strain, tear strength, hardness, and thermal stability but deteriorated the elongation at break of the nanocomposites. Based on differential scanning calorimetry, the glass transition temperature of all the nanocomposites was similar to that of the neat NR/SBR blend. Moreover, the morphology of the PS-nTiO2-filled rubber nanocomposites fractured surface analyzed by scanning electron microscopy showed an improvement in the interfacial adhesion between the rubber phase and the nanoparticles.

  3. Preparation of Azidated Polybutadiene(Az-PBD)/Ethylene-Vinyl Acetate Copolymer(EVA) Blends for the Application of Energetic Thermoplastic Elastomer

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Sang Won; Choi, Myung Chan; Chang, Young-Wook; Noh, Si-Tae [Hanyang University, Ansan (Korea, Republic of); Kwon, Soon Kil [Agency for Defense Development, Daejeon (Korea, Republic of)

    2015-02-15

    A new energetic thermoplastic elastomer based on the azidated polybutadiene(Az-PBD)/ethylene vinyl acetate copolymer (EVA) blends was prepared, and structure and properties of the blends were investigated by SEM, DSC, DMA, tensile testing and combustion test. The Az-PBD was synthesized via a two-step process involving the addition reaction of commercially available 1,2-PBD with Br{sub 2} and subsequent nucleophilic substitution reaction of the brominated PBD with NaN{sub 3}. EVA/Az-PBD with 90/10, 80/20, 70/30 (wt/wt) was prepared by a solution blending. SEM, DSC, and DMA results revealed that the blends are partially compatible and Az-PBD is dispersed in continuous EVA matrix. Tensile test showed that modulus and tension set increased while elongation-at-break of the blends decreased with increasing Az-PBD content in the blends, but all the blends showed a elongation at break as high as 700% and a tension set of less than 5%, indicating that the blends are typically elastomeric. Combustion test showed that, with increasing Az-PBD content in the blend, higher energy can be released.

  4. Immortal Ring-Opening Polymerization of rac-Lactide Using Polymeric Alcohol as Initiator to Prepare Graft Copolymer

    Directory of Open Access Journals (Sweden)

    Na Liu

    2016-01-01

    Full Text Available In the presence of a small molecular protic initiator, immortal ring-opening polymerization (ROP of lactide (LA is a highly efficient strategy to synthesize polylactide in a controllable manner, while using polymeric alcohol as an initiator has been less investigated. A series of polymeric alcohols (PS–OH composed of styrene and 4.3%–18% hydroxyl functional styrene (diethyl(hydroxy(4-vinylphenylmethylphosphonate, St–OH were synthesized through reversible addition-fragmentation transfer (RAFT polymerization. Using PS–OH as an initiator, the immortal ROP of rac-LA was catalyzed by dibutylmagnesium (MgnBu2 under various ratios of monomer to hydroxyl group within PS–OH to generate polystyrene-g-polylactide (PS–g–PLA copolymers with different graft lengths. After thermal annealing at 115 °C, the PLA domain aggregated to nanospheres among the PS continuum. The size of the nanospheres, varying from 130.1 to 224.2 nm, was related to the graft density and length of PS–g–PLA. Nanoporous films were afforded through chemical etching of the PLA component.

  5. Preparation of hollow TiO2 nanoparticles through TiO2 deposition on polystyrene latex particles and characterizations of their structure and photocatalytic activity

    Science.gov (United States)

    2012-01-01

    In a mixed solvent of water and ethanol, polystyrene/titanium dioxide (PSt/TiO2) composite particles of core-shell structure were prepared by hydrolysis of tetrabutyl titanate in the presence of cationic PSt particles or anionic PSt particles surface-treated using γ-aminopropyl triethoxysilane. Hollow TiO2 particles were obtained through calcination of the PSt/TiO2 core-shell particles to burn off the PSt core or through dissolution of the core by tetrahydrofuran (THF). An alternative process constituted of preheating the PSt/TiO2 particles at 200°C to allow partial crystallization followed by calcination or PSt dissolution by THF. The outcome TiO2 particles thus prepared were examined by TEM, and hollow TiO2 particles were observed. The crystalline phase structure and phase transformation were characterized, which revealed that preheating before the removal of the PSt core was useful to achieve the desired hollow TiO2 particles, and the calcination process was beneficial to the formation of anatase and rutile structures. The tests of TiO2 particles as catalyst in the photodegradation of Rhodamine B demonstrated that a much higher catalytic activity was observed with the TiO2 hollow particles prepared through calcination combined with preheating. PMID:23176612

  6. Bioinspired catecholic copolymers for antifouling surface coatings.

    Science.gov (United States)

    Cho, Joon Hee; Shanmuganathan, Kadhiravan; Ellison, Christopher J

    2013-05-01

    We report here a synthetic approach to prepare poly(methyl methacrylate)-polydopamine diblock (PMMA-PDA) and triblock (PDA-PMMA-PDA) copolymers combining mussel-inspired catecholic oxidative chemistry and atom transfer radical polymerization (ATRP). These copolymers display very good solubility in a range of organic solvents and also a broad band photo absorbance that increases with increasing PDA content in the copolymer. Spin-cast thin films of the copolymer were stable in water and showed a sharp reduction (by up to 50%) in protein adsorption compared to those of neat PMMA. Also the peak decomposition temperature of the copolymers was up to 43°C higher than neat PMMA. The enhanced solvent processability, thermal stability and low protein adsorption characteristics of this copolymer makes it attractive for variety of applications including antifouling coatings on large surfaces such as ship hulls, buoys, and wave energy converters.

  7. Prevalence of latex hypersensitivity among health care workers in Malaysia.

    Science.gov (United States)

    Shahnaz, M; Azizah, M R; Hasma, H; Mok, K L; Yip, E; Ganesapillai, T; Suraiya, H; Nasuruddin, B A

    1999-03-01

    Health care workers have been reported to constitute one of the few high-risk groups related to IgE-mediated hypersensitivity associated with the use of latex products. This paper describes the first ever study of prevalence carried out in Malaysia among these workers. One hundred and thirty health care personnel from Hospital Kuala Lumpur were skin tested. Extracts used were prepared from seven different brands of natural rubber latex gloves with varying levels of extractable protein (EPRRIM). Out of the 130 volunteers, 4 (3.1%) had positive skin test to latex with extracts with high levels of EPRRIM (> 0.7 mg/g). The prevalence among the Malaysian health care workers can be considered to be low in comparison to that of some consumer countries as the USA which reported a prevalence of as high as 16.9%.

  8. The effect of hydrophilic and hydrophobic block length on the rheology of amphiphilic diblock Polystyrene-b-Poly(sodium methacrylate) copolymers prepared by ATRP

    NARCIS (Netherlands)

    Raffa, Patrizio; Stuart, Marc C.A.; Broekhuis, Antonius A.; Picchioni, Francesco

    2014-01-01

    Following our previous investigation on the effect of molecular architecture on the rheology of Polystyrene-b-Poly(sodium methacrylate) copolymers (PS-b-PMAA), we consider here diblock PS-b-PMAA copolymers characterized by a different length of either the hydrophilic or the hydrophobic block. Variou

  9. Properties of starch-polyglutamic acid (PGA) graft copolymer prepared by microwave irradiation - Fourier transform infrared spectroscopy (FTIR) and rheology studies

    Science.gov (United States)

    The rheological properties of waxy starch-'-polygutamic acid (PGA) graft copolymers were investigated. Grafting was confirmed by FTIR spectroscopy. The starch-PGA copolymers absorbed water and formed gels, which exhibited concentration-dependent viscoelastic solid properties. Higher starch-PGA conce...

  10. The latex story.

    Science.gov (United States)

    Raulf, Monika

    2014-01-01

    The milky sap of the rubber tree Hevea brasiliensis is the source of the commercial production of natural rubber latex (NRL) devices, and also represents a source of potent allergenic proteins. NRL materials were introduced in the health care field in about 1840 with the advent of technical abilities to produce suitable and flexible NRL materials for medical products, especially gloves. In the late 1980s, with the increase of transmittable diseases, particularly HIV infection, the use of NRL gloves increased dramatically. During the 1990s, NRL emerged as a major cause of clinically relevant allergy in health care workers using NRL gloves and spina bifida patients with operation on the first day. The increased recognition of NRL allergies, the enhanced research on allergen characterization and sensitization mechanisms, and education about this allergy in health care facilities combined with the introduction of powder-free gloves with reduced protein levels are all factors associated with a decline in the number of suspected cases of NRL allergies in the late 1990s. NRL allergy is a very good example of a 'new allergy' that suddenly arises with tremendous health and economic implications, and also of an allergy which becomes history in a relatively short period of time based on successful primary prevention strategies by strict allergen avoidance.

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

    Energy Technology Data Exchange (ETDEWEB)

    Sari, Ahmet; Alkan, Cemil; Karaipekli, Ali; Oenal, Adem [Department of Chemistry, Gaziosmanpasa University, 60240, Tokat (Turkey)

    2008-02-15

    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

  12. EVALUATION OF LOW-VOC LATEX PAINTS

    Science.gov (United States)

    The paper gives results of an evaluation of four commercially available low-VOC (volatile organic compound) latex paints as substitutes for conventional latex paints by assessing both their emission characteristics and their performance as coatings. Bulk analysis indicated that ...

  13. Current prevalence rate of latex allergy

    National Research Council Canada - National Science Library

    Miaozong Wu; James McIntosh; Jian Liu

    2016-01-01

      Objectives: This article aims to review the current prevalence rate of latex allergy among healthcare workers, susceptible patients, and the general public, and to investigate why latex is still a ubiquitous...

  14. Preparation of methacrylic acid copolymer S nano-fibers using a solvent-based electrospinning method and their application in pharmaceutical formulations.

    Science.gov (United States)

    Hamori, Mami; Shimizu, Yuki; Yoshida, Kaori; Fukushima, Keizo; Sugioka, Nobuyuki; Nishimura, Asako; Naruhashi, Kazumasa; Shibata, Nobuhito

    2015-01-01

    In this study, we applied an electrospinning (ES) method, which is mainly employed in the textile industry, to the field of pharmaceuticals. We developed and modified an ES instrument and then utilized it to produce methacrylic acid copolymer S (MAC) nano-fibers to prepare tablets. By attaching a conductor rod made from stainless steel to the central part of the nano-fiber-collection plate of the ES apparatus, a MAC nano-fiber sheet could be produced effectively. In addition, we studied various operating conditions for this new ES method, including needle gauge, voltage between the electrodes, distance between the needle and nano-fiber-collection plate and the flow rate of MAC polymer solution, but these had no significant effect on the diameter of MAC nano-fibers. On the other hand, the viscosity (concentration) of MAC polymer solution and permittivity of solvent used to dilute MAC were closely related to the mean diameter of the nano-fibers. Tableting of MAC nano-fibers was performed using a tableting machine without lubricants, and addition of Tween 20 to the tablets enabled regulation of the release profile of a water-soluble drug. The modified ES method reported here is a useful technique for the controlled-release of drugs and has wide-ranging potential for pharmaceutical applications.

  15. Testing the vesicular morphology to destruction: birth and death of diblock copolymer vesicles prepared via polymerization-induced self-assembly.

    Science.gov (United States)

    Warren, Nicholas J; Mykhaylyk, Oleksandr O; Ryan, Anthony J; Williams, Mark; Doussineau, Tristan; Dugourd, Philippe; Antoine, Rodolphe; Portale, Giuseppe; Armes, Steven P

    2015-02-11

    Small angle X-ray scattering (SAXS), electrospray ionization charge detection mass spectrometry (CD-MS), dynamic light scattering (DLS), and transmission electron microscopy (TEM) are used to characterize poly(glycerol monomethacrylate)55-poly(2-hydroxypropyl methacrylate)x (G55-Hx) vesicles prepared by polymerization-induced self-assembly (PISA) using a reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization formulation. A G55 chain transfer agent is utilized to prepare a series of G55-Hx diblock copolymers, where the mean degree of polymerization (DP) of the membrane-forming block (x) is varied from 200 to 2000. TEM confirms that vesicles with progressively thicker membranes are produced for x = 200-1000, while SAXS indicates a gradual reduction in mean aggregation number for higher x values, which is consistent with CD-MS studies. Both DLS and SAXS studies indicate minimal change in the overall vesicle diameter between x = 400 and 800. Fitting SAXS patterns to a vesicle model enables calculation of the membrane thickness, degree of hydration of the membrane, and the mean vesicle aggregation number. The membrane thickness increases at higher x values, hence the vesicle lumen must become smaller if the external vesicle dimensions remain constant. Geometric considerations indicate that this growth mechanism lowers the total vesicle interfacial area and hence reduces the free energy of the system. However, it also inevitably leads to gradual ingress of the encapsulated water molecules into the vesicle membrane, as confirmed by SAXS analysis. Ultimately, the highly plasticized membranes become insufficiently hydrophobic to stabilize the vesicle morphology when x exceeds 1000, thus this PISA growth mechanism ultimately leads to vesicle "death".

  16. The effects of latex additions on centrifugally cast concrete for internal pipeline protection

    Energy Technology Data Exchange (ETDEWEB)

    Buchheit, R.G.; Hinkebein, T.E.; Hlava, P.F. [Sandia National Labs., Albuquerque, NM (United States); Melton, D.G. [LaQue Center for Corrosion Technology, Inc., Wrightsville Beach, NC (United States)

    1993-07-01

    Centrifugally-cast concrete liners applied to the interiors of plain steel pipe sections were tested for corrosion performance in brine solutions. An American Petroleum Institute (API) standard concrete, with and without additions of a styrene-butadiene copolymer latex, was subjected to simulated service and laboratory tests. Simulated service tests used a mechanically pumped test manifold containing sections of concrete-lined pipe. Linear polarization probes embedded at steel-concrete interfaces tracked corrosion rates of these samples as a function of exposure time. Laboratory tests used electrochemical impedance spectroscopy to study corrosion occurring at the steel-concrete interfaces. Electron probe microanalysis (EPMA) determined ingress and distribution of damaging species, such as Cl, in concrete liners periodically returned from the field. Observations of concrete-liner fabrication indicate that latex loading levels were difficult to control in the centrifugal-casting process. Overall, test results indicate that latex additions do not impart significant improvements to the performance of centrifugally cast liners and may even be detrimental. Corrosion at steel-concrete interfaces appears to be localized and the area fraction of corroding interfaces can be greater in latex-modified concretes than in API baseline material. EPMA shows higher interfacial Cl concentration in the latex-modified concretes than in the API standard due to rapid brine transport through cracks to the steel surface.

  17. Liquid ethylene-propylene copolymers

    Science.gov (United States)

    Rhein, R. A.; Ingham, J. D.; Humphrey, M. F.

    1975-01-01

    Oligomers are prepared by heating solid ethylene-propylene rubber in container that retains solid and permits liquid product to flow out as it is formed. Molecular weight and viscosity of liquids can be predetermined by process temperature. Copolymers have low viscosity for given molecular weight.

  18. Preparation, property of the complex of carboxymethyl chitosan grafted copolymer with iodine and application of it in cervical antibacterial biomembrane

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yu [School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Yang, Yumin; Liao, Qingping [Zhejiang Sanchuang Biological Technology Co., Ltd., Jiaxing, Zhejiang Province 314031 (China); Yang, Wei [School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Ma, Wanfeng [Zhejiang Sanchuang Biological Technology Co., Ltd., Jiaxing, Zhejiang Province 314031 (China); Zhao, Jian [Department of Gynaecology and Obstetrics, The First Hospital of Peking University, Beijing 100034 (China); Zheng, Xionggao [School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Yang, Yang [Zhejiang Sanchuang Biological Technology Co., Ltd., Jiaxing, Zhejiang Province 314031 (China); Chen, Rui [Department of Gynaecology and Obstetrics, The First Hospital of Peking University, Beijing 100034 (China)

    2016-10-01

    Cervical erosion is one of the common diseases of women. The loop electrosurgical excisional procedure (LEEP) has been used widely in the treatment of the cervical diseases. However, there are no effective wound dressings for the postoperative care to protect the wound area from further infection, leading to increased secretion and longer healing time. Iodine is a widely used inorganic antibacterial agent with many advantages. However, the carrier for stable iodine complex antibacterial agents is lack. In the present study, a novel iodine carrier, Carboxymethyl chitosan-g-(poly(sodium acrylate)-co-polyvinylpyrrolidone) (CMCTS-g-(PAANa-co-PVP), was prepared by graft copolymerization of sodium acrylate (AANa) and N-vinylpyrrolidone (NVP) to a carboxymethyl chitosan (CMCTS) skeleton. The obtained structure could combine prominent property of poly(sodium acrylate) (PAANa) anionic polyelectrolyte segment and good complex property of polyvinylpyrrolidone (PVP) segment to iodine. The bioactivity of CMCTS could also be kept. The properties of the complex, CMCTS-g-(PAANa-co-PVP)-I{sub 2}, were studied. The in vitro experiment shows that it has broad-spectrum bactericidal effects to virus, fungus, gram-positive bacteria and gram-negative bacteria. A CMCTS-g-(PAANa-co-PVP)-I{sub 2} complex contained cervical antibacterial biomembrane (CABM) was prepared. The iodine release from the CABM is pH-dependent. The clinic trial results indicate that CABM has better treatment effectiveness than the conventional treatment in the postoperative care of the LEEP operation. - Highlights: • The multifunctional iodine complexing carrier CMCTS-g-(PAANa-co-PVP) was prepared. • CMCTS-g-(PAANa-co-PVP)-I{sub 2} with high antibacterial property and bio-safety was studied. • By compositing it with CMCTS and gelatin further, CABM with multifunction was deduced. • The releasing properties of the activated iodine from CABM showed pH sensitivity. • CABM showed good treating effect for

  19. Parametric characterizations in superparamagnetic latex

    Indian Academy of Sciences (India)

    Seda Beyaz; Hakan Kockar; Taner Tanrisever

    2014-05-01

    The effect of synthesis parameters on the production of superparamagnetic latex, which are magnetite nanoparticles covered with a poly(methyl methacrylate) layer, were studied. The synthesis method was based on the developed route of emulsifier-free emulsion polymerization. Under this study, effects of the monomer and initiator concentrations, the amount of magnetic sol, the stirring rate and the adding rate of the magnetic sol on the properties of synthesized latexes were investigated. The characterizations were performed by a high resolution transmission electron microscopy, a dynamic light scattering, a vibrating sample magnetometer and a gel permeation chromatography. The results showed that the monomer concentration was found to be the most effective parameter on latex stability. As the initiator amount and the stirring rate increased, saturation magnetization and average molecular weight decreased due to the reactions occurring between surfaces of magnetite nanoparticles and initiator fragments. On increasing amount of magnetic sol, the saturation magnetization and polymer molecular weight increased but the size of nanospheres was unchanged because of the ions in magnetic sol. It was seen that the desired size and magnetic properties of the latex could be obtained since the parameters were found to have substantial impact on their properties.

  20. Latex Allergy - A Case Report

    Directory of Open Access Journals (Sweden)

    Dr. Athma Prasanna

    2005-10-01

    Full Text Available The usage of rubber and its products are not uncommon in various walks of life. A continuous exposure or contact may sensitize the human body, causing reactions from mild to fatal. Despite the availability of the literature, medical personnel are still unaware of the implications of the use of latex materials.

  1. Latex allergy and filaggrin null mutations

    DEFF Research Database (Denmark)

    Carlsen, Berit C; Meldgaard, Michael; Hamann, Dathan

    2011-01-01

    Objectives Natural rubber latex (NRL) contains over 200 proteins of which 13 have been identified as allergens and the cause of type I latex allergy. Health care workers share a high occupational risk for developing latex allergy. Filaggrin null mutations increase the risk of type I sensitization...... in the cases in this study may not have occurred through direct skin contact but through the respiratory organs via latex proteins that are absorbed in glove powder and aerosolized......Objectives Natural rubber latex (NRL) contains over 200 proteins of which 13 have been identified as allergens and the cause of type I latex allergy. Health care workers share a high occupational risk for developing latex allergy. Filaggrin null mutations increase the risk of type I sensitizations...

  2. Integration of latex protein sequence data provides comprehensive functional overview of latex proteins.

    Science.gov (United States)

    Cho, Won Kyong; Jo, Yeonhwa; Chu, Hyosub; Park, Sang-Ho; Kim, Kook-Hyung

    2014-03-01

    The laticiferous system is one of the most important conduit systems in higher plants, which produces a milky-like sap known as latex. Latex contains diverse secondary metabolites with various ecological functions. To obtain a comprehensive overview of the latex proteome, we integrated available latex proteins sequences and constructed a comprehensive dataset composed of 1,208 non-redundant latex proteins from 20 various latex-bearing plants. The results of functional analyses revealed that latex proteins are involved in various biological processes, including transcription, translation, protein degradation and the plant response to environmental stimuli. The results of the comparative analysis showed that the functions of the latex proteins are similar to those of phloem, suggesting the functional conservation of plant vascular proteins. The presence of latex proteins in mitochondria and plastids suggests the production of diverse secondary metabolites. Furthermore, using a BLAST search, we identified 854 homologous latex proteins in eight plant species, including three latex-bearing plants, such as papaya, caster bean and cassava, suggesting that latex proteins were newly evolved in vascular plants. Taken together, this study is the largest and most comprehensive in silico analysis of the latex proteome. The results obtained here provide useful resources and information for characterizing the evolution of the latex proteome.

  3. Copolymers For Capillary Gel Electrophoresis

    Science.gov (United States)

    Liu, Changsheng; Li, Qingbo

    2005-08-09

    This invention relates to an electrophoresis separation medium having a gel matrix of at least one random, linear copolymer comprising a primary comonomer and at least one secondary comonomer, wherein the comonomers are randomly distributed along the copolymer chain. The primary comonomer is an acrylamide or an acrylamide derivative that provides the primary physical, chemical, and sieving properties of the gel matrix. The at least one secondary comonomer imparts an inherent physical, chemical, or sieving property to the copolymer chain. The primary and secondary comonomers are present in a ratio sufficient to induce desired properties that optimize electrophoresis performance. The invention also relates to a method of separating a mixture of biological molecules using this gel matrix, a method of preparing the novel electrophoresis separation medium, and a capillary tube filled with the electrophoresis separation medium.

  4. HIGH SOLIDS-CONTENT NANOSIZE POLYMER LATEXES MADE BY A MODIFIED EMULSION COPOLYMERIZATION

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yuying; GUO Tianying; HAO Guangjie; SONG Maodao; Zhang Banghua

    2003-01-01

    Polymer nanoparticles were prepared in the methyl methacrylate (MMA)/buty lmethacrylate (BA) emulsion copolymerization process by a modified microemulsion copolymerization method. 2-Hydroxyethyl methacrylate(HEMA), acrylate (AA) and methyl acrylate (MAA) were used as reactive cosurfactants. With this process high polymer: surfactant weight ratios (40:1 or greater),relatively concentrated (~30wt. %) latexes and small (~60nm) particle diameters were obtained.Properties of the latexes were characterized by TEM, DSC, dynamic light scattering, and IR spectroscopy.

  5. A Robust Cross-Linking Strategy for Block Copolymer Worms Prepared via Polymerization-Induced Self-Assembly

    Science.gov (United States)

    2016-01-01

    A poly(glycerol monomethacrylate) (PGMA) chain transfer agent is chain-extended by reversible addition–fragmentation chain transfer (RAFT) statistical copolymerization of 2-hydroxypropyl methacrylate (HPMA) with glycidyl methacrylate (GlyMA) in concentrated aqueous solution via polymerization-induced self-assembly (PISA). A series of five free-standing worm gels is prepared by fixing the overall degree of polymerization of the core-forming block at 144 while varying its GlyMA content from 0 to 20 mol %. 1H NMR kinetics indicated that GlyMA is consumed much faster than HPMA, producing a GlyMA-rich sequence close to the PGMA stabilizer block. Temperature-dependent oscillatory rheological studies indicate that increasing the GlyMA content leads to progressively less thermoresponsive worm gels, with no degelation on cooling being observed for worms containing 20 mol % GlyMA. The epoxy groups in the GlyMA residues can be ring-opened using 3-aminopropyltriethoxysilane (APTES) in order to prepare core cross-linked worms via hydrolysis-condensation with the siloxane groups and/or hydroxyl groups on the HPMA residues. Perhaps surprisingly, 1H NMR analysis indicates that the epoxy–amine reaction and the intermolecular cross-linking occur on similar time scales. Cross-linking leads to stiffer worm gels that do not undergo degelation upon cooling. Dynamic light scattering studies and TEM analyses conducted on linear worms exposed to either methanol (a good solvent for both blocks) or anionic surfactant result in immediate worm dissociation. In contrast, cross-linked worms remain intact under such conditions, provided that the worm cores comprise at least 10 mol % GlyMA. PMID:27134311

  6. Novel 4-Arm Poly(Ethylene Glycol-Block-Poly(Anhydride-Esters Amphiphilic Copolymer Micelles Loading Curcumin: Preparation, Characterization, and In Vitro Evaluation

    Directory of Open Access Journals (Sweden)

    Li Lv

    2013-01-01

    Full Text Available A novel 4-arm poly(ethylene glycol-block-poly(anhydride-esters amphiphilic copolymer (4-arm PEG-b-PAE was synthesized by esterization of 4-arm poly(ethylene glycol and poly(anhydride-esters which was obtained by melt polycondensation of α-, ω-acetic anhydride terminated poly(L-lactic acid. The obtained 4-arm PEG-b-PAE was characterized by 1H-NMR and gel permeation chromatography. The critical micelle concentration of 4-arm PEG-b-PAE was 2.38 μg/mL. The curcumin-loaded 4-arm PEG-b-PAE micelles were prepared by a solid dispersion method and the drug loading content and encapsulation efficiency of the micelles were 7.0% and 85.2%, respectively. The curcumin-loaded micelles were spherical with a hydrodynamic diameter of 151.9 nm. Curcumin was encapsulated within 4-arm PEG-b-PAE micelles amorphously and released from the micelles, faster in pH 5.0 than pH 7.4, presenting one biphasic drug release pattern with rapid release at the initial stage and slow release later. The hemolysis rate of the curcumin-loaded 4-arm PEG-b-PAE micelles was 3.18%, which was below 5%. The IC50 value of the curcumin-loaded micelles against Hela cells was 10.21 μg/mL, lower than the one of free curcumin (25.90 μg/mL. The cellular uptake of the curcumin-loaded micelles in Hela cell increased in a time-dependent manner. The curcumin-loaded micelles could induce G2/M phase cell cycle arrest and apoptosis of Hela cells.

  7. Synthesis and characterization of polymer-silica hybrid latexes and sol-gel-derived films

    Science.gov (United States)

    Petcu, Cristian; Purcar, Violeta; Ianchiş, Raluca; Spătaru, Cătălin-Ilie; Ghiurea, Marius; Nicolae, Cristian Andi; Stroescu, Hermine; Atanase, Leonard-Ionuţ; Frone, Adriana Nicoleta; Trică, Bogdan; Donescu, Dan

    2016-12-01

    Sol-gel derived organic-inorganic hybrid systems were obtained by applying alkaline-catalyzed co-hydrolysis and copolycondensation reactions of tetraethoxysilane (TEOS), methyltriethoxysilane (MTES), isobutyltriethoxysilane (IBTES), diethoxydimethylsilane (DMDES), and vinyltriethoxysilane (VTES), respectively, into a polymer latex functionalized with vinyltriethoxysilane (VTES). The properties of the latex hybrid materials were analyzed by FTIR, water contact angle, environmental scanning electron microscopy (ESEM), TEM and AFM analysis, respectively. FT-IR spectra confirmed that the chemical structures of the sol-gel derived organic-inorganic materials are changed as function of inorganic precursor and Sisbnd Osbnd Si networks are formed during the co-hydrolysis and copolycondensation reactions. The water contact angle on the sol-gel latex film containing TEOS + VTES increased to 135° ± 2 compared to 65° ± 5 for the blank latex, due VTES incorporation into latex material. TGA curves of hybrid sample modifies against neat polymer, the thermal stability being influenced by the presence of the inorganic partner. ESEM analysis showed that the latex hybrid films prepared with different inorganic precursors were formed and the Si-based polymers were distributed on the surface of the dried sol-gel hybrid films. TEM and AFM photos revealed that the latex emulsion morphology was modified due to the VTES incorporation into system.

  8. Biocompatible and Biodegradable Ultrafine Nanoparticles of Poly(Methyl Methacrylate-co-Methacrylic Acid Prepared via Semicontinuous Heterophase Polymerization: Kinetics and Product Characterization

    Directory of Open Access Journals (Sweden)

    Henned Saade

    2016-01-01

    Full Text Available Ultrafine nanoparticles, less than 10 nm in mean diameter, of the FDA approved copolymer methyl methacrylate- (MMA- co-methacrylic acid (MAA, 2/1 (mol/mol, were prepared. The method used for the preparation of these particles stabilized in a latex containing around 11% solids includes the dosing of the monomers mixture on a micellar solution preserving monomer starved conditions. It is thought that the operation at these conditions combined with the hydrophilicity of MMA and MAA units favors the formation of ultrafine particles; the propagation reaction carried out within so small compartments renders copolymer chains rich in syndiotactic units very likely as consequence of the restricted movements of the end propagation of the chains. Because of their biocompatibility and biodegradability as well as their extremely small size these nanoparticles could be used as vehicles for improved drug delivery in the treatment of chronic-degenerative diseases.

  9. Relevance of latex aeroallergen for healthcare workers

    Directory of Open Access Journals (Sweden)

    X. Baur

    1996-01-01

    Full Text Available The dispersion of latex allergen bound on glove powder has been shown to be of clinical importance to latex-sensitized medical staff and patients. To investigate whether latex aeroallergen is associated with the development of latex allergic reactions in health care workers, air samples were collected in 33 hospital rooms and two physicians' offices. Concentrations of latex allergens in the samples were determined by a competitive inhibition immunoassay and related to reported hypersensitivity reactions and to specific IgE results of 111 staff members engaged in these rooms. Latex aeroallergen (up to 205 ng/m3 could be detected in all rooms where powdered latex gloves were used and ventilation systems were not installed. Conjunctivitis (n=10, rhinitis (n=12 and dyspnea (n=4 were reported exclusively by employees working in such contaminated rooms. Also workers with latex-specific IgE antibodies (n=l 7 were found only in these rooms. Urticaria in personnel (n=26 was reported in rooms with and without detectable allergen load. All symptoms were significantly associated with latex-specific IgE antibodies. Our results demonstrate that immediate-type sensitization and allergic symptoms are associated with detectable latex aeroallergen.

  10. The participation ratios of cement matrix and latex network in latex cement co-matrix strength

    Directory of Open Access Journals (Sweden)

    Ahmed M. Diab

    2014-06-01

    Full Text Available This investigation aims to determine the participation ratio of cement matrix and latex network in latex cement co-matrix strength. The first stage of this study was carried out to investigate the effect of styrene butadiene rubber (SBR on cement matrix participation ratio by measuring degree of hydration and compressive strength. The second stage in this study shows an attempt to evaluate the latex participation ratio in mortar and concrete strength with different latex chemical bases. Effect of latex particle size on latex network strength was studied. The test results indicated that the latex participation ratio in co-matrix strength is influenced by type of cement matrix, type of curing, latex type, latex solid/water ratio, strength type and age. For modified concrete, when the SBR solid/water ratio increases the latex participation ratio in flexural and pull out bond strength increases. The latex participation ratio in co-matrix strength decreases as latex particle size increases.

  11. Nitrile versus Latex for Glove Juice Sampling.

    Science.gov (United States)

    Landers, Timothy F; Dent, Anthony

    2014-01-01

    The objective of this study was to explore the utility of nitrile gloves as a replacement for latex surgical gloves in recovering bacteria from the hands. Two types of nitrile gloves were compared to latex gloves using the parallel streak method. Streaks of Klebsiella pneumoniae and Staphylococcus aureus were made on tryptic soy agar plates, and the zones of inhibition were measured around pieces of glove material placed on the plates. Latex gloves produced a mean zone of inhibition of 0.28 mm, compared to 0.002 mm for nitrile gloves (platex in glove juice sampling methods, since nitrile avoids the risk of latex exposure.

  12. An Evaluation of Ethylene-Vinyl Acetate Copolymers as Desensitizers for RDX in Insensitive Booster Compositions Prepared by the Slurry Coating Technique

    Science.gov (United States)

    1989-08-01

    dried at ti (Yp. p pr^ to us., The EVA copolymers examined were selected f~r the Elvay (I~u Pv:!A’,, Levapren ( Bayer ) and Vyndthone (US InCoistrial...addition micro-encapsulation technigue (MLM-3348). Miamisburg, Ohio: Monsanto Research Corporation, Mound. 34. Vannet, M.D. and Ball, G.L. (1987). Journal of

  13. Synthesis and properties of acrylate latex modified by vinyl alkoxy siloxane

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Acrylate latex modified by vinyl triisopropoxy silane (C-1706) was synthesized by seeded emulsion polymerization with anionic emulsifier sodium dodecyl sulphonate(SDS) and nonionic emulsifier OP-10 as the multiple emulsifiers at (78±2) ℃. The effects of different factors, such as the emulsifier, C-1706 monomer and its feeding manner on the properties of aciylate latex modified by C-1706 were investigated. The particle size distribution and the structure, the configuration, the weather durability and stain resistance of copolymer latex were characterized by particle size analyzer, Fourier transform infrared spectroscopy (FT-IR), transmission electron microscope(TEM), scanning electron microscope(SEM) and ultraviolet aging instrument respectively. The results show that SDS to OP-10 as multiple emulsifiers can lead to coordinated efficiency, the optimal emulsifier dosage is 2.4%-3.2%(mass fraction), and the mass ratio of SDS to OP-10 is 1:1- 1:2. The seeded emulsion polymerization can effectively introduce a organic-siloxane bonding in a macromolecule inter polymer, and the obtained acrylate latex modified by organic-siloxane possesses narrow distribution of particle size with mean diameter of 51.8-76.6 nm and has the excellent properties in weather durability and stain-resistance especially.

  14. Latex Allergy with Discus Form of Inhalation Drug of Asthma

    Directory of Open Access Journals (Sweden)

    Ogun Sezer

    2009-10-01

    Full Text Available The prevalence of latex allergy in healthcare workers and which was taken chronic medical therapy has significantly increased during the last 15 years. Latex allergy generally refers to a type 1 reaction to natural rubber latex (NRL proteins with clinical manifestations ranging from contact urticaria to asthma and anaphylaxis. In this report, we discuss latex allergy with discus form of inhalation drug of asthma after contact of discus form to lips. Still, latex allergy is an important problem in patients with latex allergy. We must inform all patients about latex allergy and all latex containing devices. [TAF Prev Med Bull 2009; 8(5.000: 451-452

  15. Thermo-responsive release of curcumin from micelles prepared by self-assembly of amphiphilic P(NIPAAm-co-DMAAm)-b-PLLA-b-P(NIPAAm-co-DMAAm) triblock copolymers.

    Science.gov (United States)

    Hu, Yanfei; Darcos, Vincent; Monge, Sophie; Li, Suming; Zhou, Yang; Su, Feng

    2014-12-10

    Thermo-responsive micelles are prepared by self-assembly of amphiphilic triblock copolymers composed of a poly(l-lactide) (PLLA) central block and two poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide) (P(NIPAAm-co-DMAAm)) lateral blocks, using solvent evaporation/film hydration method. The resulting micelles exhibit very low critical micelle concentration (CMC) which slightly increases from 0.0113 to 0.0144 mg mL(-1) while the DMAAm content increases from 31.8 to 39.4% in the hydrophilic P(NIPAAm-co-DMAAm) blocks. The lower critical solution temperatures (LCST) of copolymers varies from 44.7 °C to 49.4 °C in water as determined by UV spectroscopy, and decreases by ca. 3.5 °C in phosphate buffered saline (PBS). Curcumin was encapsulated in the core of micelles. High drug loading up to 20% is obtained with high loading efficiency (>94%). The LCST of drug loaded micelles ranges from 37.5 to 38.0 °C with drug loading increasing from 6.0 to 20%. The micelles with diameters ranging from 47.5 to 88.2 nm remain stable over one month due to the negative surface charge as determined by zeta potential (-12.4 to -18.7 mV). Drug release studies were performed under in vitro conditions at 37 °C and 40 °C, i.e. below and above the LCST, respectively. Initial burst release is observed in all cases, followed by a slower release. The release rate is higher at 40 °C than that at 37 °C due to thermo-responsive release across the LCST. On the other hand, micelles with lower drug loading exhibit higher release rate than those with higher drug loading, which is assigned to the solubility effect. Peppas' theory was applied to describe the release behaviors. Moreover, the in vitro cytotoxicity of copolymers was evaluated using MTT assay. The results show that the copolymers present good cytocompatibility. Therefore, the nano-scale size, low CMC, high drug loading and stability, as well as good biocompatibility indicate that these thermo-responsive triblock copolymer micelles

  16. Effect of irradiation on the prevulcanized latex/low nitrosamines latex blends

    Energy Technology Data Exchange (ETDEWEB)

    Ibrahim, Pairu; Zin, Wan Manshol Wan [Malaysian Nuclear Agency, 43000 kajang, Selangor (Malaysia); Daik, Rusli [Faculty of Science and Technology, Universiti Kebangsaan Malaysia,43600 bangi, Selangor (Malaysia)

    2015-09-25

    Radiation Prevulcanized Natural Rubber Latex (RVNRL) was blended with Low Nitrosamines Latex (LNL) at different composition ratio. Methyl Metachrylate (MMA) was added for grafting onto the blended latex. Blended latex was subjected to gamma irradiation at various doses up to 8kGy. The mechanical properties and FTIR analysis were investigated as a function of the blended composition and irradiation dose. It was found that blending at specific ratio and gamma irradiation at specific dose led to significant improvement on the properties of the latex. The optimum mechanical properties was attained at a total blending ratio of 70% RVNRL and 30% of LNL.

  17. Effect of irradiation on the prevulcanized latex/low nitrosamines latex blends

    Science.gov (United States)

    Ibrahim, Pairu; Daik, Rusli; Zin, Wan Manshol Wan

    2015-09-01

    Radiation Prevulcanized Natural Rubber Latex (RVNRL) was blended with Low Nitrosamines Latex (LNL) at different composition ratio. Methyl Metachrylate (MMA) was added for grafting onto the blended latex. Blended latex was subjected to gamma irradiation at various doses up to 8kGy. The mechanical properties and FTIR analysis were investigated as a function of the blended composition and irradiation dose. It was found that blending at specific ratio and gamma irradiation at specific dose led to significant improvement on the properties of the latex. The optimum mechanical properties was attained at a total blending ratio of 70% RVNRL and 30% of LNL.

  18. Block copolymer membranes for aqueous solution applications

    KAUST Repository

    Nunes, Suzana Pereira

    2016-03-22

    Block copolymers are known for their intricate morphology. We review the state of the art of block copolymer membranes and discuss perspectives in this field. The main focus is on pore morphology tuning with a short introduction on non-porous membranes. The two main strategies for pore formation in block copolymer membranes are (i) film casting and selective block sacrifice and (ii) self-assembly and non-solvent induced phase separation (SNIPS). Different fundamental aspects involved in the manufacture of block copolymer membranes are considered, including factors affecting the equilibrium morphology in solid films, self-assembly of copolymer in solutions and macrophase separation by solvent-non-solvent exchange. Different mechanisms are proposed for different depths of the SNIPS membrane. Block copolymer membranes can be prepared with much narrower pore size distribution than homopolymer membranes. Open questions and indications of what we consider the next development steps are finally discussed. They include the synthesis and application of new copolymers and specific functionalization, adding characteristics to respond to stimuli and chemical environment, polymerization-induced phase separation, and the manufacture of organic-inorganic hybrids.

  19. Latex Allergy In Health Care Workers

    Directory of Open Access Journals (Sweden)

    Hayriye Sarıcaoğlu

    2013-05-01

    Full Text Available Background and Design: We aimed to determine the frequency of latex allergy in our hospital and to to evaluate the clinical and demographical features of the cases.Materials and Methods: A detailed questionnaire was administered to healthcare workers by a physician. Skin prick test with latex and patch test with rubber chemicals and a piece of latex glove were performed for all healthcare workers. Latex-specific IgE was measured in serum.Results: The study sample consisted of 36 nurses, 14 doctors, and 50 healthcare workers. While 46 subjects had symptoms, 54 subjects had no symptoms. The relationship of clinical disease with working duration, exposure duration (hour/day, history of atopy, and drug/food allergies was statistically significant. Five nurses and 1 healthcare worker had positive skin prick test. Two of them had positive latex-specific IgE. Positive skin prick test statistically significantly correlated with occupation, working duration, exposure duration (hour/day and positive latex-specific IgE. Two nurses and 2 healthcare workers had positive latex-specific IgE. Two of them had positive skin prick test. Positive latexspecific IgE statistically significantly correlated with working duration, exposure duration, and positive skin prick test. Patch test with a piece of latex glove was negative in all subjects. Three healthcare workers had positive patch test with thiuram-mix, one of them had also positive patch test with mercaptobenzothiazole.Discussion: One of the risk factors for latex allergy is occupations involving frequent exposure to latex products. Latex allergy should be taken into consideration if type I hypersensitivity reactions occur in occupational groups at risk for anaphylactic reaction.

  20. Graphene-philic surfactants for nanocomposites in latex technology.

    Science.gov (United States)

    Mohamed, Azmi; Ardyani, Tretya; Bakar, Suriani Abu; Brown, Paul; Hollamby, Martin; Sagisaka, Masanobu; Eastoe, Julian

    2016-04-01

    Graphene is the newest member of the carbon family, and has revolutionized materials science especially in the field of polymer nanocomposites. However, agglomeration and uniform dispersion remains an Achilles' heel (even an elephant in the room), hampering the optimization of this material for practical applications. Chemical functionalization of graphene can overcome these hurdles but is often rather disruptive to the extended pi-conjugation, altering the desired physical and electronic properties. Employing surfactants as stabilizing agents in latex technology circumvents the need for chemical modification allowing for the formation of nanocomposites with retained graphene properties. This article reviews the recent progress in the use of surfactants and polymers to prepare graphene/polymer nanocomposites via latex technology. Of special interest here are surfactant structure-performance relationships, as well as background on the roles surfactant-graphene interactions for promoting stabilization.

  1. Polyether-polyester graft copolymer

    Science.gov (United States)

    Bell, Vernon L. (Inventor)

    1987-01-01

    Described is a polyether graft polymer having improved solvent resistance and crystalline thermally reversible crosslinks. The copolymer is prepared by a novel process of anionic copolymerization. These polymers exhibit good solvent resistance and are well suited for aircraft parts. Previous aromatic polyethers, also known as polyphenylene oxides, have certain deficiencies which detract from their usefulness. These commercial polymers are often soluble in common solvents including the halocarbon and aromatic hydrocarbon types of paint thinners and removers. This limitation prevents the use of these polyethers in structural articles requiring frequent painting. In addition, the most popular commercially available polyether is a very high melting plastic. This makes it considerably more difficult to fabricate finished parts from this material. These problems are solved by providing an aromatic polyether graft copolymer with improved solvent resistance and crystalline thermally reversible crosslinks. The graft copolymer is formed by converting the carboxyl groups of a carboxylated polyphenylene oxide polymer to ionic carbonyl groups in a suitable solvent, reacting pivalolactone with the dissolved polymer, and adding acid to the solution to produce the graft copolymer.

  2. 新型药物载体聚乙醇-聚丙交酯载药颗粒的制备及表征%Preparation and characterization of biodegradable nanoparticles from methoxy poly(ethylene glycol)-poly(D,L-lactide)block copolymers as novel drug carriers

    Institute of Scientific and Technical Information of China (English)

    姜维; 王运东; 张建铮; 甘泉; 张汉威; 贝建中; 赵秀文; 费维扬

    2006-01-01

    Methoxy poly(ethylene glycol)-poly(D,L-lactide) block copolymers (PEG-PLA) were prepared through ring-opening polymerization.The oil in water suspension method was used to prepare block copolymer micelles. The critical micelle concentration (CMC) by fluorescence spectroscopy was 0.0056 mg·ml-1. The physical state of the inner core region of micelles was characterized with 1HNMR. The size of indomethacin (IMC) loaded micelles measured by dynamic light scattering (DLS) showed narrow monodisperse size distribution and the average diameters were less than 50 nm. In addition, the nanoparticles with relatively high drug loading content (DLC) were obtained.

  3. Ficus carica latex-mediated synthesis of silver nanoparticles and its application as a chemophotoprotective agent.

    Science.gov (United States)

    Borase, Hemant P; Patil, Chandrashekhar D; Suryawanshi, Rahul K; Patil, Satish V

    2013-10-01

    The present work provides scientific support on the use of latex of Ficus carica to synthesize stable silver nanoparticles (AgNPs). AgNPs synthesized immediately after the addition of latex to silver nitrate solution at room temperature. Synthesized nanoparticles were of spherical shape with average size of 163.7 nm. Fourier transform infrared spectroscopy analysis revealed capping of proteins and phenolic compound on AgNPs, while X-ray diffraction analysis confirmed the fcc nature of AgNPs. Particles formed were stable for a long time (6 months). It was found that incorporation of AgNPs with 2 and 4% concentration exhibits synergistic increase in sun protection factor of commercial sunscreen and natural extracts ranging from 01 to 12,175% than control. Further characterization of latex and AgNPs revealed total phenolic content of 98.75 and 94.88 μg/ml. The ferric ion reduction potentials of latex and AgNPs were 79.69 and 18.79%. Reduction potential of ascorbic acid was synergistically increased after cumulative preparation of ascorbic acid with latex and AgNPs and found to be 106.76 and 101.50% for ascorbic acid + latex and ascorbic acid + AgNPs, respectively.

  4. LOW DENSITY POLYETHYLENE/CLAY NANOCOMPOSITES MODIFIED BY ETHYLENE COPOLYMERS: EFFECTS OF FUNCTIONALIZED SEGMENTS ON MORPHOLOGY

    Institute of Scientific and Technical Information of China (English)

    Bo Xu; Yi-hu Song; Yong-gang ShangGuan; Qiang Zheng

    2006-01-01

    Melt extrusion was used to prepare binary nanocomposites of ethylene copolymers and organoclay and trinary nanocomposites of low-density polyethylene (LDPE), ethylene copolymer and organoclay. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were used to analyze the structure of the clay phase and the morphology of the nanocomposites. Influences of the comonomer in the copolymer and the content of the copolymer on the morphology of the resulting nanocomposites were discussed. The binary and the trinary composites may form intercalated or exfoliated structures depending on the interaction between the copolymer and the clay layers and the content of the copolymer.

  5. 功能化PDMS/PMMA核壳乳胶粒子的制备与表征%Preparation and characterization of functional PDMS / PMMA core-shell latex particles

    Institute of Scientific and Technical Information of China (English)

    王权; 刘喜军; 伊海楠

    2012-01-01

    A novel latex particles of polysiloxane/polymethylmethacrylate (PDMS/PMMA) having core-shell structure was successfully synthesized by the pre-emulsion semi-continuous seeded emulsion polymerization. Through the introduction of functional monomer ITA, MAH or GMA to realize the function of core-shell latex particles.Which were characterized by the laser particle size analyzer. Fourier transform infrared spectroscopy (FTIR) and transmission electron microscope (TEM).%采用预乳化-半连续种子乳液聚合工艺合成了聚硅氧烷,聚甲基丙烯酸甲酯(PDMS/PMMA)核壳乳胶粒子,通过引入功能单体ITA、MAH或GMA实现核壳乳胶粒子的功能化。采用激光粒度分析仪、傅立叶变换红外光谱仪(FTIR)和透射电子显微镜(TEM)等手段对核壳乳胶粒子进行了表征。

  6. Latex improvement of recycled asphalt pavement

    Science.gov (United States)

    Drennon, C.

    1982-08-01

    The performance of a single unmodified milled recycled asphalt concrete was compared to milled asphalt concrete modified by addition of three types of rubber latex. Latex was added at 2, 3, 5, and 8 percent latex by weight of asphalt in the asphalt concrete. Lattices used were a styrene butadiene (SBR), a natural rubber (NR), an acrylonitrile butadiene (NBR), and four varieties of out of specification SBR lattices. Marshall tests, while indecisive, showed a modest improvement in properties of SBR and NR added material at 3 and 5 percent latex. Addition of NBR latex caused deterioration in Marshall stability and flow over that of control. Repeated load tests were run using the indirect tensile test, analyzed by the VESYS program, which computes life of pavements. Repeated load tests showed improvement in asphalt concrete life when 3 and 5 percent SBR was added. Improvement was also shown by the out of specification SBR.

  7. Jackfruit anaphylaxis in a latex allergic patient.

    Science.gov (United States)

    Wongrakpanich, Supakanya; Klaewsongkram, Jettanong; Chantaphakul, Hiroshi; Ruxrungtham, Kiat

    2015-03-01

    Several fruits have been reported to crossreact with latex antigen in latex allergy patients but little is known regarding tropical fruits in particular. Here we report the case of a 34-year old nurse who developed anaphylaxis following the ingestion of dried jackfruit (Artocarpus heterophyllus). The patient had a history of chronic eczema on both hands resulting from a regular wear of latex gloves. She and her family also had a history of atopy (allergic rhinitis and/or atopic dermatitis). The results of skin prick tests were positive for jackfruit, latex glove, kiwi and papaya, but the test was negative for banana. While we are reporting the first case of jackfruit anaphylaxis, further research needs to be conducted to identify the mechanisms underlying it. In particular, in-vitro studies need to be designed to understand if the anaphylaxis we describe is due to a cross reactivity between latex and jackfruit or a coincidence of allergy to these 2 antigens.

  8. Preparation of non-aggregated fluorescent nanodiamonds (FNDs) by non-covalent coating with a block copolymer and proteins for enhancement of intracellular uptake.

    Science.gov (United States)

    Lee, Jong Woo; Lee, Seonju; Jang, Sangmok; Han, Kyu Young; Kim, Younggyu; Hyun, Jaekyung; Kim, Seong Keun; Lee, Yan

    2013-05-01

    Fluorescent nanodiamonds (FNDs) are very promising fluorophores for use in biosystems due to their high biocompatibility and photostability. To overcome their tendency to aggregate in physiological solutions, which severely limits the biological applications of FNDs, we developed a new non-covalent coating method using a block copolymer, PEG-b-P(DMAEMA-co-BMA), or proteins such as BSA and HSA. By simple mixing of the block copolymer with FNDs, the cationic DMAEMA and hydrophobic BMA moieties can strongly interact with the anionic and hydrophobic moieties on the FND surface, while the PEG block can form a shell to prevent the direct contact between FNDs. The polymer-coated FNDs, along with BSA- and HSA-coated FNDs, showed non-aggregation characteristics and maintained their size at the physiological salt concentration. The well-dispersed, polymer- or protein-coated FNDs in physiological solutions showed enhanced intracellular uptake, which was confirmed by CLSM. In addition, the biocompatibility of the coated FNDs was expressly supported by a cytotoxicity assay. Our simple non-covalent coating with the block copolymer, which can be easily modified by various chemical methods, projects a very promising outlook for future biomedical applications, especially in comparison with covalent coating or protein-based coating.

  9. Properties of natural rubber latexes modified by different processes%不同改性方法对天然胶乳的性能影响

    Institute of Scientific and Technical Information of China (English)

    廖小雪; 唐冰; 吴翠; 谭海生

    2011-01-01

    The natural rubber (NR) latex modified by chlorinated paraffin and antimony oxide blending was prepared; the NR latex addition polymerizaion modified by trichlorobromomethane was prepared;the NR latex graft copolymerization modified by tribromopropylene was prepared. A comparison of the colloidal properties, flame-resistance properties and solvent-resistance properties was made between NR latex and the three kinds of modified latex. The results showed that the viscosity of the three kinds of modified latex was higher than the non-modified latex' s, the viscosity of graft copolymerization and halogenation modified latex changed greatly,blend modified latex's viscosity had little change; the flame-resistance properties of the three kinds of modified latex were higher than the nonmodified latex's; solvent-resistance of the films of graft copolymerization modified latex and halogenation modified latex was superior to the films of non-modified latex's, solvent-resistance of the films of blend modified latex was worse than the ones of non-modified latex's.%分别采用氯化石蜡与Sb2O3共混改性天然胶乳、用三氯澳甲烷卤化加成改性天然胶乳、以3-澳丙烯接枝共聚改性天然胶乳,对3种不同工艺所制备的改性天然胶乳与未改性天然胶乳进行了胶体性能、阻燃性及耐溶剂性能的比较.研究结果表明:3种改性胶乳的粘度比未改性天然胶乳的要高,且接枝改性胶乳和卤化改性胶乳变化较大,共混改性胶乳的变化较少;3种改性胶乳的阻燃性能高于未改性天然胶乳的;卤化改性天然胶乳和接枝改性天然胶乳的耐溶剂性较好,而共混改性天然胶的耐溶剂性较差.

  10. Synthesis of imide/arylene ether copolymers for adhesives and composite matrices

    Science.gov (United States)

    Jensen, B. J.; Hergenrother, P. M.; Bass, R. G.

    1991-01-01

    A series of imide/arylene ether copolymers were prepared from the reaction of an amorphous arylene ether oligomer and a semi-crystalline imide oligomer. These copolymers were thermally characterized and mechanical properties were measured. One block copolymer was endcapped and the molecular weight was controlled to provide a material that displayed good compression moldability and attractive adhesion and composite properties.

  11. Study on the Preparation and Properties of Caprolactam and Octamethyl Cyclotetrasiloxane Copolymer%己内酰胺与八甲基环四硅氧烷共聚物的合成及性能研究

    Institute of Scientific and Technical Information of China (English)

    任庆佩; 孙丹丹; 朱晓清; 潘庆华; 马清芳; 郝超伟

    2015-01-01

    通过己内酰胺与八甲基环四硅氧烷的阴离子共聚合反应制取D4/PA6共聚物,并对其热力学和力学性能进行了系统分析.TGA分析结果表明,八甲基环四硅氧烷的加入不影响PA6的热稳定性.DSC分析结果表明,随着D4含量的增加,PA6的结晶温度和熔融温度均有先增加后减小的趋势.力学测试结果表明,含4% D4时断裂伸长率可达12.671%,其韧性有所提高.%The D4/PA6 copolymer was prepared by the copolymerization with caprolactam and octamethyl cyclotetrasiloxane ,the thermodynamic and mechanical properties of which were also analyzed .TGA analysis showed that D4 could not clearly affect the thermal stability of PA 6 .DSC analysis showed that crystallization and melting temperatures of PA6 first increased and then slightly decreased with increasing content of D 4 .And the mechanical test analysis exhibited that the elongation at break of the copolymer could approach 12 .671% with the 4% content of D4 ,which implied that the toughness of the copolymer was improved .

  12. Functional silicone copolymers and elastomers with high dielectric permittivity

    DEFF Research Database (Denmark)

    Madsen, Frederikke Bahrt; Daugaard, Anders Egede; Hvilsted, Søren

    . This was done trough the synthesis of new functionalizable siloxane copolymers [2] that allow for the attachment of high dielectric permittivity molecules through copper-catalyzed azide-alkyne 1,3-dipolar cycloaddition (CuAAC) reactions. The synthesised siloxane copolymers were prepared via the tris...

  13. Fabrication of grating-like polystyrene latex monolayer structure as three-dimensional calibration standards for scanning probe microscope

    Institute of Scientific and Technical Information of China (English)

    Zhu Guo-Dong; Zeng Zhi-Gang; Guo Zhang; Du Qiang-Guo; Yan Xue-Jian

    2009-01-01

    This paper illuminates the preparation of grating-like polystyrene latex monolayer structure, which can minimize the effects of the size deviation of spheres and the defect transfer on the accuracy as calibration samples for micro-scopes. The latex films are grown on freshly cleaved mica substrates by vertical deposition method. The concentration dependence of the structure and the topography of latex films is characterized by optical microscope, ultraviolet-visible transmission spectrum and scanning probe microscope. The origination of such a grating-like structure is also discussed.

  14. 21 CFR 801.435 - User labeling for latex condoms.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false User labeling for latex condoms. 801.435 Section... latex condoms. (a) This section applies to the subset of condoms as identified in § 884.5300 of this... products are formed from latex films. (b) Data show that the material integrity of latex condoms...

  15. Reinforcement of latex rubber by the incorporation of amphiphilic nanoparticles

    Science.gov (United States)

    Latex rubbers are fabricated from latex suspensions. During the fabrication process, latex particles are bound together while water is removed from the suspension. This report shows the mechanical properties of latex rubbers can be improved by incorporating a small amount of amphiphilic nanoparticle...

  16. Influence of viscoelasticity on the nano-micromechanical behavior of latex films and pigmented coatings

    Science.gov (United States)

    Giri, Manish

    2001-09-01

    Nano to microscale deformation behavior of different carboxylated styrene-butadiene co-polymer Latexes were investigated using a commercial nanoindentation device. The latexes differed primarily in their glass transition temperature (T g). The bulk dynamic rheological properties, as determined from a rheometer, dictate the axismmetric deformation behavior of the latexes. Results from dynamic tests performed on latexes were analyzed using the theories in contact and fracture mechanics. Two theories of linear viscoelastic fracture mechanics (LVEFM) were employed to model the adhesion hysteresis (loading-unloading cycle) curves to obtain meaningful cohesive zone (fracture process zone) parameters and a stress intensity functional (K I(t)) for an entire cycle. The stress intensity functional, extracted from the deformation behavior, is independent of the loading history and was shown to depend only on the crack propagation velocity, (da/dt), for the entire cycle. The quantitative values of stress intensities were then discussed in the light of polymer molecular phenomenon's such as viscous chain desorption. Nanoindetation was developed as a tool for systematically investigating both the bulk as well as the cohesive zone properties of viscoelastic polymers. Effect of plastic deformation on the deformation behavior of high pigment volume concentration (PVC) coatings was also analyzed. Polystyrene plastic pigment, CaCO3 and Clay pigments were used to form the coatings layers. High PVC coatings are viscoelastic due to the latex present but also contain air, the third phase, which could explain the plastic deformation if a certain critical yield stress is exceeded. At PVC's greater than 70%, the coatings showed significant plastic (permanent) deformation, which has to be accounted for in modeling the hysteresis curves. The residual plastic deformation was confirmed by imaging the indent over a period of time. Modeling the curves resulted in a compressive yield stress (sigma

  17. 两亲性双硒聚合物的制备及其聚集体形成%Preparation of Amphiphilic Diselenide Copolymer and Formation of Its Aggregates

    Institute of Scientific and Technical Information of China (English)

    顾晓瑜; 王朝阳; 童真

    2013-01-01

    Selenium has several unique biological effects in many aspects,making use of bioactive components and inorganic selenium to prepare antitumor organic selenium compounds will have a great significant impact on cancer therapy and patient wellbeing.It was well-known that Se-Se bond is very reactive and sensitive to the dual redox environment,therefore,we can take advantage of such feature to prepare diselenide-containing polymers which can be applied in the area of drug controlled release.In this paper,we prepared amphiphilic diselenide copolymers with diselenide-containing diols (HO-SeSe-OH),isophorone diisocyanate (IPDI),and water soluble low-molecular chitosan (LW-CS).The synthetic copolymers were characterized by means of gel permeation chromatography (GPC),1H NMR and FTIR spectroscopy.The molecular weight of CS-PUSeSe-CS copolymer was 4.42 × 104 g/mol which calculated according to the integral ratio of the peaks at δ 4.00 and 4.42 which related to CH2O groups of chitosan and NHCOOCH2 groups of IPDI,respectively.The size distribution of aggregates measured by dynamic light scattering (DLS) measurements,which gave a result of about 130 nm in average diameter.The critical aggregate concentration (CAC) of aggregates was measured by the fluorescent probe method and the result was 0.01 mg/mL.The dual redox responsive of aggregates was studied both in VC and H2O2 solution,the results showed that amphiphilic diselenide copolymer would cause Se-Se chain scission in no matter weak oxidative or reductive ambient environment.Although negative charged drug-rhodamine B (RB) could not release out from aggregates due to electrostatic attraction.However,positive charged drug-doxorubicin hydrochloride (Doxo) can easily release from aggregates in reductive VC solution by analyzing UV-spectra at the wavelength of 500 nm,indicating aggregates assembled from diselenide-containing copolymers may act as powerful and efficient bionano reactors and realize controllable drug delivery by

  18. Preparation and properties of itaconic anhydride-based copolymers with L-lactide%衣康酸酐与 L-丙交酯共聚物的制备与性能研究

    Institute of Scientific and Technical Information of China (English)

    滕丽晶; 张明飞; 高宗春; 汪磊; 徐晓红; 聂王焰; 周艺峰; 陈鹏鹏

    2015-01-01

    以衣康酸酐(IAn)和L‐丙交酯(LLA)为单体、辛酸亚锡为催化剂,采用熔融开环聚合的方法合成一种新型的生物基聚乳酸共聚物(IAn‐PLLA).用1 H‐NMR、GPC、DSC、TGA、XRD、水降解测试表征共聚物的结构与性能.1 H‐NMR结果表明,合成的共聚物为预期产物;DSC和TGA分析表明,随着IAn摩尔比增大,IAn‐PLLA的熔点和玻璃化转变温度降低,但仍有较好的热稳定性;磷酸盐缓冲溶液(pH=7.4)中的降解测试结果表明,随着衣康酸酐含量的增加,共聚酯的降解速率显著提高.%A novel biobased polylactide copolymer (IAn‐PLLA ) was synthesized via melting ring‐opening polymerization of itaconic anhydride (IAn ) with L‐lactide (LLA ) in the presence of stannous octoate as a catalyst .The structure and properties of the prepared copolymers were confirmed with 1 H‐NMR , GPC , DSC , TGA , XRD and hydrolytic degradation test .1 H‐NMR spectra showed that the synthetic copolymers were the expected products .DSC and TGA analysis indicated that the melting point (Tm ) and glass transition temperature(Tg ) of IAn‐PLLA decreased with the increasing of IAn reaction mole ratios , but they still had excellent thermal stability .The result of degradation tests in the phosphate buffer solution (pH=7.4) indicated that the degradation rate of copolymers had significantly increased with the increasing IAn content .

  19. Preparation and Characterization of Facilitated Transport Membranes Composed of Chitosan-Styrene and Chitosan-Acrylonitrile Copolymers Modified by Methylimidazolium Based Ionic Liquids for CO₂ Separation from CH₄ and N₂.

    Science.gov (United States)

    Otvagina, Ksenia V; Mochalova, Alla E; Sazanova, Tatyana S; Petukhov, Anton N; Moskvichev, Alexandr A; Vorotyntsev, Andrey V; Afonso, Carlos A M; Vorotyntsev, Ilya V

    2016-06-09

    CO₂ separation was found to be facilitated by transport membranes based on novel chitosan (CS)-poly(styrene) (PS) and chitosan (CS)-poly(acrylonitrile) (PAN) copolymer matrices doped with methylimidazolium based ionic liquids: [bmim][BF₄], [bmim][PF₆], and [bmim][Tf₂N] (IL). CS plays the role of biodegradable film former and selectivity promoter. Copolymers were prepared implementing the latest achievements in radical copolymerization with chosen monomers, which enabled the achievement of outstanding mechanical strength values for the CS-based membranes (75-104 MPa for CS-PAN and 69-75 MPa for CS-PS). Ionic liquid (IL) doping affected the surface and mechanical properties of the membranes as well as the gas separation properties. The highest CO₂ permeability 400 Barrers belongs to CS-b-PS/[bmim][BF₄]. The highest selectivity α (CO₂/N₂) = 15.5 was achieved for CS-b-PAN/[bmim][BF₄]. The operational temperature of the membranes is under 220 °C.

  20. Preparation and Characterization of Facilitated Transport Membranes Composed of Chitosan-Styrene and Chitosan-Acrylonitrile Copolymers Modified by Methylimidazolium Based Ionic Liquids for CO2 Separation from CH4 and N2

    Directory of Open Access Journals (Sweden)

    Ksenia V. Otvagina

    2016-06-01

    Full Text Available CO2 separation was found to be facilitated by transport membranes based on novel chitosan (CS–poly(styrene (PS and chitosan (CS–poly(acrylonitrile (PAN copolymer matrices doped with methylimidazolium based ionic liquids: [bmim][BF4], [bmim][PF6], and [bmim][Tf2N] (IL. CS plays the role of biodegradable film former and selectivity promoter. Copolymers were prepared implementing the latest achievements in radical copolymerization with chosen monomers, which enabled the achievement of outstanding mechanical strength values for the CS-based membranes (75–104 MPa for CS-PAN and 69–75 MPa for CS-PS. Ionic liquid (IL doping affected the surface and mechanical properties of the membranes as well as the gas separation properties. The highest CO2 permeability 400 Barrers belongs to CS-b-PS/[bmim][BF4]. The highest selectivity α (CO2/N2 = 15.5 was achieved for CS-b-PAN/[bmim][BF4]. The operational temperature of the membranes is under 220 °C.

  1. Preparation and characterization of PDMS/PMMA core-shell latex particles having functional group in surface layer%表层功能化PDMS/PMMA核壳乳胶粒子的制备与表征

    Institute of Scientific and Technical Information of China (English)

    张国青; 刘喜军

    2014-01-01

    In this paper, the polydimethyl siloxane/polymethyl methacrylate(PDMS/PMMA)core-shell latex particles (-320 nm)respectively with itaconic acid(ITA),maleic anhydride(MAH)and glycidyl methacrylate(GMA) as functional monomer in surface layer were successfully synthesized employing pre-emulsification semi-continuous process by seeded emulsion polymerization method. Octamethyl cyclotetrasiloxane(D 4 )and Tetravinyl tetramethyl cyelotetrasiloxane as the main monomer were compounded to form PDMS core latex particles with methyl triethoxysilane(MTES)as cross-linking agent. The effects of the reaction time, surfactant and catalyst concentration, and the ratio of D 4 and VD 4 on the polymerization system were studied, and the optimal synthesizing process of PDMS core latex particles was defined.By laser particle size analyzer, Fourier transform infrared spectrometer and transmission electron microscopy analysis showed that the core monomer conversion was nearly 85%and PDMS latex particle size was at about 290 nm when the reaction time was 10 h,surfactant concentration was 5.3%, catalyst concentration was 5.3%,and D4∶VD4=4∶1.%分别以衣康酸(ITA)、马来酸酐(MAH)和甲基丙烯酸缩水甘油酯(GMA)为功能单体,采用预乳化半连续工艺通过种子乳液聚合方法成功合成了表层功能化的聚二甲基硅氧烷/聚甲基丙烯酸甲酯(PDMS/PMMA)核壳乳胶粒子(~320 nm)。PDMS核乳胶粒子以八甲基环四硅氧烷(D 4)和四甲基四乙烯基环四硅氧烷(VD 4)为单体、甲基三乙氧基硅烷(MTES)为交联剂构建而成,实验研究了反应时间、乳化剂和催化剂用量、单体D 4与VD 4比例对聚合体系的影响,并确定了PDMS核乳胶粒子合成最佳工艺。通过激光粒度分析仪、傅里叶变换红外光谱仪、透射电子显微镜等分析表明:当反应时间为10 h、乳化剂用量为核单体总量的5.3%、催化剂用量为核单体总量的5.3%

  2. [Latex allergy in a population at risk].

    Science.gov (United States)

    Ruiz Fernández, M; Flores Sandoval, G; Orea Solano, M

    1999-01-01

    The allergy to latex is an illness whose prevalence has been increased in very significant form in the last years. To know the allergy incidence to latex in population of risk, as well as to identify the related sintomatology and the importance or paper that play the atopia antecedents and time of contact with latex for the development of the illness. We carry out a prospective, descriptive, experimental and traverse study in population of risk, in the service of Allergy and clinical Immunology of the Hospital Regional Lic. Adolfo López Mateos, ISSSTE. One hundred patients of both sexes were included, with age of 20 to 50 years, with the antecedent of being personal medical and paramedic and to have presented contact with latex material in a minimum period of one year. They were carried out clinical history with registration of sintomatology nasal, bronchial, cutaneous and associated to contact with latex. They were carried out cutaneous test for prick to latex with positive control with the help of histamine solution and negative control with solution of Evans and immediate reading of the same one. 22% of the patients in study, they presented positive skin test latex, with a time of exhibition 10 year-old average, 68% presented antecedent of atopy personal, family and, likewise the associate sintomatology was in a 33.3% dermatology, 54.5 nasal, nobody presented bronchial symptoms and a 9% asymptomatic was reported. We support that the immediate skin test latex for Prick is an important parameter of support diagnosis for allergy to type 1 latex.

  3. Regenerated cellulose fibers spun-dyed with carbon black/latex composite dispersion.

    Science.gov (United States)

    Wang, Chunxia; Du, Changsen; Tian, Anli; Fu, Shaohai; Xu, Changhai

    2014-01-30

    A carbon black (CB)/latex composite was prepared by the method of miniemulsion polymerization for use as a colorant for spun dyeing of regenerated cellulose fibers. Analysis of experimental results revealed that the CB/latex composite had a small particle size and a narrow particle size distribution which were important to ensure a stable dispersion being later added to spinning solution. A good stability of the prepared CB/latex composite dispersion in the spinning solution indicated that it was highly possible to use the CB/latex composite as a colorant for spun dyeing of regenerated cellulose fibers. When a 3.5% mass ratio of CB/latex composite to cellulose was used for spun dyeing, the spun-dyed fibers had the highest tensile strength, breaking elongation and color strength. The rubbing and washing color fastnesses of spun-dyed regenerated cellulose fibers could satisfy requirements of most textiles. This study provided a new insight into producing spun-dyed regenerated cellulose with a novel colorant.

  4. EFFECT OF THE PHASE STRUCTURE EVOLUTION ON THE PROPERTIES OF FILMS FORMED FROM PBA/P(ST-CO-MMA)COMPOSITE LATEX

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A group of heterogeneous latexes poly(butyl acrylate)/poly(styrene-co-methyl methacrylate)(PBA/P(St-co-MMA))were prepared by a semi-continuous seeded emulsion polymerization process under monomer starved conditions.The glass transition temperature(Tg)and the mechanical properties of the film formed from the composite latex changed with the evolution of the particle morphology.A photon transmission method was used to monitor the phase structure evolution of films which were prepared from core-shell PBA/P(St-co-MMA)latex at room temperature and annealed at 383 K above Tg of the polymers.In addition,the changes of the surface of the film formed from the composite latex with time at 383 K were observed by AFM.The evidence illustrated that the film formed from the core-shell latex particles was metastable.The rearrangement of the phases could occur under proper conditions.

  5. Non-woven fibrous materials with antibacterial properties prepared by tailored attachment of quaternized chitosan to electrospun mats from maleic anhydride copolymer.

    Science.gov (United States)

    Ignatova, Milena; Petkova, Zhanina; Manolova, Nevena; Markova, Nadya; Rashkov, Iliya

    2012-01-01

    In order to impart antibacterial properties to microfibrous electrospun materials from styrene/maleic anhydride copolymers, quaternized chitosan derivatives (QCh) containing alkyl substituents of different chain lengths are covalently attached to the mats. A complete inhibition of the growth of bacteria, S. aureus (Gram-positive) and E. coli (Gram-negative), for a contact time of 30–120 min or a decrease of the bacterial titer by 2–3 log units is observed depending on the quaternization degree, the chain length of the alkyl substituent, and the molar mass of QCh. The modified mats are also effective in suppressing the adhesion of pathogenic S. aureus bacteria.

  6. Physical adsorption of anisotropic titania nanoparticles onto poly(2-vinylpyridine) latex and characterisation of the resulting nanocomposite particles.

    Science.gov (United States)

    Fielding, Lee A; Armes, Steven P; Staniland, Paul; Sayer, Robert; Tooley, Ian

    2014-07-15

    Four poly(2-vinylpyridine) latexes with intensity-average mean diameters ranging between 246 and 955nm were prepared by aqueous emulsion polymerisation. These latexes were characterised by transmission electron microscopy, field emission scanning electron microscopy, dynamic light scattering, aqueous electrophoresis, disc centrifuge photosedimentometry and thermogravimetry. The adsorption of rice grain-shaped nano-sized titania particles onto the surface of these latex particles from aqueous solution was investigated. It was found that the titania particles adsorb strongly at pH 10 and the optimal loading and packing density of titania was investigated for each latex. The resulting core-shell P2VP-titania nanocomposite particles were characterised in terms of their titania contents, surface coverages and colloidal stabilities. UV-Vis spectra were recorded for the titania nanoparticles, the original P2VP latexes and the poly(2-vinylpyridine)-titania nanocomposite particles. It was found that, for the larger nanocomposite particles, UV-Vis absorption was dominated by the latex core, whereas the smaller P2VP-titania nanocomposite particles exhibited UV attenuation to longer wavelengths compared to both the bare latex and the titania particles. The poly(2-vinylpyridine) cores were selectively removed by calcination of the nanocomposite particles and the resulting hollow titania structures were investigated by transmission electron microscopy.

  7. Effectiveness and feasibility of methanol extracted latex of Calotropis procera as larvicide against dengue vectors of western Rajasthan, India.

    Science.gov (United States)

    Singhi, Manju; Purohit, Anil; Chattopadhyay, Sushmita

    2015-06-01

    Identification of novel effective larvicide from natural resources is essential to combat developing resistances, environmental concerns, residue problems and high cost of synthetic insecticides. Results of earlier laboratory findings have shown that Calotropis procera extracts showed larvicidal, ovicidal and refractory properties towards ovipositioning of dengue vectors; further, latex extracted with methanol was found to be more effective compared to crude latex. For testing efficacy and feasibility of extracted latex in field, the present study was undertaken in different settings of Jodhpur City, India against dengue vectors. Study areas were selected based on surveillance design for the control of dengue vectors. During the study period domestic and peri-domestic breeding containers were treated with methanol extracted latex and mortality was observed after 24 h as per WHO guidelines. Latex was manually collected from internodes of Calotropis procera and extracted using methanol (AR) grade. Methanol extracted latex of C. procera was found effective and feasible larvicide against dengue vectors in the field conditions. Cement tanks, clay pots and coolers (breeding sites) were observed as key containers for the control of dengue transmission. Today environmental safety is considered to be very important. Herbal composition prepared by the extraction of latex of C. procera can be used as an alternative approach for the control of dengue vectors. This will reduce the dependence on expensive products and stimulate local efforts to enhance the public involvement.

  8. Exercise with latex sport bands represents a risk for latex allergic patients.

    Science.gov (United States)

    Untersmayr, Eva; Lukschal, Anna; Hemmer, Wolfgang; Harwanegg, Christian; Breiteneder, Heimo; Jarisch, Reinhard; Scheiner, Otto; Jensen-Jarolim, Erika

    2008-01-29

    Based on two clinical observations of adverse reactions during exercise with latex sport bands, we aimed to assess the possible risk for allergic patients posed by this equipment by investigating allergen content and IgE binding potential. Protein extracts of three different latex sport bands were characterized with sera of latex allergic patients. The IgE recognition profile of the allergic patients was identified by component resolved diagnosis and the allergen composition of the extracts was characterized by inhibition assays with the recombinant latex allergens Hev b 1, 3, 5, 6.02, and 8. The sera showed pronounced IgE binding to all three blotted extracts, however with diverse patterns. Inhibition assays revealed the presence of Hev b 1, 3, 5, and 8 in latex sport band extracts. The clinical relevance of contained allergens was demonstrated by strong skin reactions when testing with latex sport bands. From our results we conclude that latex sport bands contain clinically relevant allergens and may cause latex allergic individuals to experience allergic symptoms, potentially amplified by exercise-induced mechanisms. Even though latex is labeled on products, it is important that patients as well as athletic trainers and physical therapists recognize the risk of adverse reactions with these bands.

  9. Induction of cell self-organization on weakly positively charged surfaces prepared by the deposition of polyion complex nanoparticles of thermoresponsive, zwitterionic copolymers.

    Science.gov (United States)

    Iwai, Ryosuke; Haruki, Ryota; Nemoto, Yasushi; Nakayama, Yasuhide

    2017-07-01

    We have developed inducible cell self-organization through weakly positively charged culture surfaces. In this study, a thermoresponsive and zwitterionic copolymer comprised of N,N-dimethylaminoethyl methacrylate (DMAEMA) and methacrylic acid (MA) (PDMAEMA-co-PMA; Mn: ∼9.7 × 10(4) g/mol; PDMAEMA/PMA ratio: 10) was designed for inducing cell self-organization. The copolymer formed single polymer-derived polyion complex (sPIC) nanoparticles following dissolution in an aqueous solution. The sPIC nanoparticles had a positive charge (ca. 25 mV). Self-organization occurred in adipose-derived vascular stromal cell monolayers cultivated on sPIC-deposited surfaces. There were dramatic morphological changes of these cells with the formation of capillary-like networks and single-cell aggregates with little cytotoxicity. This was a significant improvement compared with cells grown on previously developed surfaces deposited with PIC, a mixture of PDMAEMA and plasmid DNA. Thus, sPICs of PDMAEMA-co-PMA may allow for the accurate evaluation of a variety of cell behaviors with less cytotoxicity, and may facilitate additional potential medical applications such as cell-based therapy and drug discovery. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 1009-1015, 2017. © 2016 Wiley Periodicals, Inc.

  10. [Latex ligation in treatment of chronic hemorrhoids].

    Science.gov (United States)

    Ektov, V N; Somov, K A

    2015-01-01

    We analyzed the results of treatment of 432 patients with chronic hemorrhoids using different variants of latex ligation. New technique including ligation of mucosa and submucosa of low-ampullar rectum providing ligation of hemorrhoidalvessels, lifting and recto-anal repair is developed and suggested. This method is advisable to use in case of chronic internal hemorrhoids stages I and II. The authors recommend simultaneous combined ligation of mucosa of low-ampullar rectum and internal hemorrhoids for stages III and IV. Different variants of latex ligation with external hemorrhoids excision were used in 103 patients. Pointed variants of latex ligation preserve important advantages including mini-invasiveness, simplicity and wide availability, low cost. Good remote results were obtained after these procedures in 87.3% of observations. Suggested tactics extends use of latex ligation and increases its effectiveness in treatment of different stages and forms of chronic hemorrhoids.

  11. Allergy to latex in health workers

    Directory of Open Access Journals (Sweden)

    Fajardo-Zapata, Álvaro L.

    2015-01-01

    Full Text Available Introduction: A common and growing problem in hospitals is hypersensitivity to rubber latex antigens, since many products, including gloves, are manufactured from this material, with the consequent possibility of producing allergy in persons who use them. Objective: To find out if health workers at a fourth level clinic in Bogotá, Colombia, are allergic to rubber latex, in relation to the use of gloves. Materials and methods: Descriptive, cross-sectional study of a non-probabilistic intentional-type sample in each one of four hospital units. A survey was applied to participants. Results: 16 of the 26 persons (61.5% with history of allergic processes manifested some kind of reaction when they had contact with latex gloves; the problem was more significant in the nursing personnel compared to physicians. Conclusions: The exposure to latex gloves may be generating the appearance of allergic occupational disease in health workers.

  12. Latex glove sensitivity amongst diagnostic imaging healthcare ...

    African Journals Online (AJOL)

    kemrilib

    of symptoms, causal agents and awareness of latex glove reactions amongst four ... radiologists, radiographers, radiology nurses and darkroom technicians who ... surgery. Scientific data has proven that gloves serve as a two-way barrier ...

  13. IDENTIFICATION OF BACTERIA IN LATEX PAINTS

    Directory of Open Access Journals (Sweden)

    Rojas, J.

    2008-01-01

    Full Text Available The bacteria are prokaryote organisms with a high capacity to colonize many types of habits. This research was developed with the object to identify extremophiles bacteria presents in latex paint. The bacteria were cultivated in culture mediums TSA, Blood Agar, Mc Conkey and finally the biochemical proof API-NF® for bacteria's isolation and identification, respectively. Characterization showed bacterial profile of Pasteurella sp. Hypothesis that could be found extremophiles bacteria in latex paint were demonstrated.

  14. Shell morphology of core-shell latexes based on conductive polymers

    NARCIS (Netherlands)

    Huijs, F.M; Vercauteren, F.F.; de Ruiter, B.; Kalicharan, D; Hadziioannou, G

    Core-shell latexes with a conductive shell can be used to prepare transparent conducting layers. We have focussed on the relation between the conducting polymer content and the shell morphology and on its influence on conductivity. At low polypyrrole (PPy) concentrations the shell has a smooth

  15. Fabrication of latex rubber reinforced with micellar nanoparticle as an interface modifier

    Science.gov (United States)

    Reinforced latex rubbers were fabricated by incorporating small amount of nanoparticles as interface modifier. The rubbers were fabricated in a compression mold at 130°C. The incorporated nanoparticles were prepared from wheat protein (gliadin) and ethyl cyanoacrylate (ECA). These nanoparticles were...

  16. Latex particle template lift-up guided gold wire-networks via evaporation lithography

    KAUST Repository

    Lone, Saifullah

    2014-01-01

    We describe a hybrid methodology that combines a two dimensional (2D) monolayer of latex particles (with a pitch size down to 1 μm) prepared by horizontal dry deposition, lift-up of a 2D template onto flat surfaces and evaporation lithography to fabricate metal micro- and nano wire-networks. This journal is

  17. Preparation and Cross-Linking of All-Acrylamide Diblock Copolymer Nano-Objects via Polymerization-Induced Self-Assembly in Aqueous Solution

    Science.gov (United States)

    2017-01-01

    Various carboxylic acid-functionalized poly(N,N-dimethylacrylamide) (PDMAC) macromolecular chain transfer agents (macro-CTAs) were chain-extended with diacetone acrylamide (DAAM) by reversible addition–fragmentation chain transfer (RAFT) aqueous dispersion polymerization at 70 °C and 20% w/w solids to produce a series of PDMAC–PDAAM diblock copolymer nano-objects via polymerization-induced self-assembly (PISA). TEM studies indicate that a PDMAC macro-CTA with a mean degree of polymerization (DP) of 68 or higher results in the formation of well-defined spherical nanoparticles with mean diameters ranging from 40 to 150 nm. In contrast, either highly anisotropic worms or polydisperse vesicles are formed when relatively short macro-CTAs (DP = 40–58) are used. A phase diagram was constructed to enable accurate targeting of pure copolymer morphologies. Dynamic light scattering (DLS) and aqueous electrophoresis studies indicated that in most cases these PDMAC–PDAAM nano-objects are surprisingly resistant to changes in either solution pH or temperature. However, PDMAC40–PDAAM99 worms do undergo partial dissociation to form a mixture of relatively short worms and spheres on adjusting the solution pH from pH 2–3 to around pH 9 at 20 °C. Moreover, a change in copolymer morphology from worms to a mixture of short worms and vesicles was observed by DLS and TEM on heating this worm dispersion to 50 °C. Postpolymerization cross-linking of concentrated aqueous dispersions of PDMAC–PDAAM spheres, worms, or vesicles was performed at ambient temperature using adipic acid dihydrazide (ADH), which reacts with the hydrophobic ketone-functionalized PDAAM chains. The formation of hydrazone groups was monitored by FT-IR spectroscopy and afforded covalently stabilized nano-objects that remained intact on exposure to methanol, which is a good solvent for both blocks. Rheological studies indicated that the cross-linked worms formed a stronger gel compared to linear precursor

  18. Nylon 46-polytetramethylene oxide segmented block copolymers

    NARCIS (Netherlands)

    Gaymans, R.J.; Schwering, P.; Haan, de J.L.

    1989-01-01

    Block copolymers were synthesized from amine-terminated polytetramethylene oxide (PMTO) (Mw 800 and 1130) and polyamide 4,6 salt. First prepolymers were prepared at 200–210°C in the presence of a solvent (pyrrolidone). The prepolymers were postcondensed at 255°C (where possible in the solid state) t

  19. Gyroid Membranes made from Nanoporous Blck Copolymers

    DEFF Research Database (Denmark)

    Szewczykowski, Piotr Plzemystaw; Vigild, Martin Etchells; Ndoni, Sokol;

    2007-01-01

    of the membrane and its nanoporosity is e.g. obtained by cross-linking the majority blocks and selectively etching the minority blocks. Here we report on ultrafiltration membranes prepared from a 1,2-polybutadiene-b-polydimethylsiloxane diblock copolymer with gyroid structure. Different experimental methods...

  20. Glycine/Glycolic acid based copolymers

    NARCIS (Netherlands)

    in 't Veld, P.J.A.; in 't Veld, Peter J.A.; Shen, Zheng-Rong; Shen, Z.; Takens, Gijsbert A.J.; Takens, G.A.J.; Dijkstra, Pieter J.; Feijen, Jan

    1994-01-01

    Glycine/glycolic acid based biodegradable copolymers have been prepared by ring-opening homopolymerization of morpholine-2,5-dione, and ring-opening copolymerization of morpholine-2,5-dione and glycolide. The homopolymerization of morpholine-2,5-dione was carried out in the melt at 200°C for 3 min

  1. LEDs based on conjugated PPV block copolymers

    NARCIS (Netherlands)

    Brouwer, H.J.; Hilberer, A.; Krasnikov, V.V.; Werts, M.; Wildeman, J.; Hadziioannou, G.

    1997-01-01

    A way to control the bandgap in semi-conducting polymers is by preparing polymers with a partially conjugated backbone. In our laboratory, three conjugated copolymers containing PPV trimers as light emitting chromophores have been synthesized, which emit in the blue, green and orange wavelength regi

  2. Glycine/Glycolic acid based copolymers

    NARCIS (Netherlands)

    Veld, in 't Peter J.A.; Shen, Zheng-Rong; Takens, Gijsbert A.J.; Dijkstra, Pieter J.; Feijen, Jan

    1994-01-01

    Glycine/glycolic acid based biodegradable copolymers have been prepared by ring-opening homopolymerization of morpholine-2,5-dione, and ring-opening copolymerization of morpholine-2,5-dione and glycolide. The homopolymerization of morpholine-2,5-dione was carried out in the melt at 200°C for 3 min u

  3. Silicon containing copolymers

    CERN Document Server

    Amiri, Sahar; Amiri, Sanam

    2014-01-01

    Silicones have unique properties including thermal oxidative stability, low temperature flow, high compressibility, low surface tension, hydrophobicity and electric properties. These special properties have encouraged the exploration of alternative synthetic routes of well defined controlled microstructures of silicone copolymers, the subject of this Springer Brief. The authors explore the synthesis and characterization of notable block copolymers. Recent advances in controlled radical polymerization techniques leading to the facile synthesis of well-defined silicon based thermo reversible block copolymers?are described along with atom transfer radical polymerization (ATRP), a technique utilized to develop well-defined functional thermo reversible block copolymers. The brief also focuses on Polyrotaxanes and their great potential as stimulus-responsive materials which produce poly (dimethyl siloxane) (PDMS) based thermo reversible block copolymers.

  4. Substrate tolerant direct block copolymer nanolithography

    DEFF Research Database (Denmark)

    Li, Tao; Wang, Zhongli; Schulte, Lars

    2016-01-01

    Block copolymer (BC) self-assembly constitutes a powerful platform for nanolithography. However, there is a need for a general approach to BC lithography that critically considers all the steps from substrate preparation to the final pattern transfer. We present a procedure that significantly...... simplifies the main stream BC lithography process, showing a broad substrate tolerance and allowing for efficient pattern transfer over wafer scale. PDMS-rich poly(styrene-b-dimethylsiloxane) (PS-b-PDMS) copolymers are directly applied on substrates including polymers, silicon and graphene. A single oxygen...

  5. “活”的α-甲基苯乙烯共聚物:聚合反应新化学和材料工程新技术%A Novel Macroinitiator Based on the Copolymer of α-Methylstyrene Synthesis and Its Application in Preparing Block and Graft Polymers

    Institute of Scientific and Technical Information of China (English)

    马育红; 张冰; 赵长稳; 刘莲英; 蒋姗; 梁淑君; 杨万泰

    2013-01-01

    Due to the steric hindrance effects in combination with stability of the tertiary benzylic a-methylstyryl radical, there is a dynamic equilibrium between the monomer a-methylstyrene (AMS) and its polymer (PAMS) when the temperature is greater than 61 ℃ (the ceiling polymerization temperature). Based on this unique feature, a novel strategy to prepare co-polymers of AMS having liable bonds as potential macromolecular free radical initiators for synthesizing block and graft copolymers has been successfully developed in our laboratory. By conventional free radical polymerization, a series of AMS copolymers, including copolymers with (meth)acrylate, acrylic acid, styrene and maleic anhydride were synthesized. Typically, with the increasing of AMS fraction in monomer feed, the rate of copolymerization was significantly retarded and the molecular weight of the copolymers was reduced. However, the copolymer yield could be as high as 90% (w) with the increased addition of initiator, up to 4% (w), and the molar fraction of AMS structural unit in AMS copolymers could be up to 25% (mol%). It has been demonstrated that the copolymers containing AMS structural units are efficient free radical initiators when the temperature is greater than 80 ℃ (much better higher than 90 ℃). These copolymers could be exploited as macroinitiator in preparing block copolymers and core-shell polymer particles by bulk, solution and emulsion polymerization processes. In addition, the experimental results demonstrated that the molecular weight of copolymer products prepared with AMS copolymers as macromolecular initiators increased steadily with the monomer conversion. Though the polymerization initiated by AMS copolymers was not a well-controlled living system yet, it showed some characteristics of living polymerization. The ESR spectrum presented direct evidence of the generation of carbon centered radicals in the products of copolymer of AMS with glycidyl methacrylate (PAG) heated with j

  6. Preparation of composite of block copolymer/gold nanoparticle based alginate polysaccharide%海藻多糖基嵌段共聚物/纳米金复合物的制备

    Institute of Scientific and Technical Information of China (English)

    刘意; 吴石楷; 李金炜; 孙福强; 崔英德

    2014-01-01

    Objective The composite was prepared in situ about polyvinyl pyrrolidone block copolymer/nano-gold ( SA-330-S2-Au ) based alginate polysaccharides. Methods The dithioester base alginate polysaccharides was synthesised at first, and then used as a chain transfer agent ( CTA ) for RAFT polymerization, to sythesis polyvinyl pyrrolidone block copolymer ( SA-330-S2 ) based alginate polysaccharides. By the self-assembly properties of SA-330-S2 ,the composite of polyvinyl pyrrolidone block copolymer/nano-gold ( SA-330-S2-Au ) based alginate polysaccharides was prepared in situ, and characterized by using methods such as FT-IR,NMR,DSC,TEM and SEM et al. Results The size of the gold nanoparticles was about 10-30 nm . But the average particle size of composite nanoparticles was about 54.4 nm when it was measured by the method of DLS in wet. Due to the stabilizing effect of block copolymers based seaweed polysaccharide of the shell layer of composite nanoparticles,the storage of SA-330-S2-Au aqueous was more than six months,and there was significant fluorescence. Conclusion The SA-330-S2-Au aqueous solution is very stable with fluorescence properties,and is expected to be used in tumor diagnosis and treatment.%目的:原位法制备海藻多糖基聚乙烯基吡咯烷酮嵌段共聚物/纳米金复合物( SA-330-S2-Au)。方法首先合成改性海藻多糖基二硫代酯,并用作RAFT聚合的链转移剂(CTA),制备海藻多糖基聚乙烯基吡咯烷酮嵌段的共聚物( SA-330-S2),然后利用SA-330-S2自组装特性,原位法制备SA-330-S2-Au,并用FT-IR、NMR、DSC、TEM、SEM等方法进行分析表征。结果复合物SA-330-S2-Au中的纳米金粒子大小约10~30 nm,湿态时纳米复合纳米粒子的平均粒径约为54.4 nm,由于复合纳米粒子外壳层的海藻多糖基嵌段共聚物的稳定化作用,SA-330-S2-Au水溶液储存期超过6个月,且有明显荧光。结论 SA-330-S2-Au水溶液稳定且具有荧光特性,有望应用于肿瘤诊疗领域。

  7. New synthesis of amphiphilic copolymers PE-g-PEO via esterfication

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    A new series of high molecular weight amphiphilic graft copolymers PE-g-PEO has been prepared. The esterifications between PE-p-MS-g-MA and PEO with OH group at the chain end are carried out under different conditions. The compositions of these graft copolymers are studied by NMR and FTIR. It is found to be a convenient and efficient way to prepare high molecular weight PE-g-PEO graft copolymers.

  8. SYNTHESIS OF STYRENE-METHYL METHACRYLATE BLOCK COPOLYMER BY POLYAZOAMIDE AS INITIATOR

    Institute of Scientific and Technical Information of China (English)

    WANG Zhongyi; WEI Jeqing

    1996-01-01

    Polyazoamide(PAA) was used as initiator to prepare block copolymer P(MMA-b-St) by free radical polymerization. The fraction of block copolymer was about 50%. The structure of the block-copolymer was characterized by IR and the results of 1H-NMR and GPC showed that the content of the block and the molecular weight (-Mw) of the prepolymer and block copolymer could be controlled by varying the mol ratio of styrene/PAA and MMA/prepolymer. DSC and TEM results revealed that the block copolymer has two separated glass transition temperatures and phase separation within the domain structure.

  9. Anti-ulcer activity of Synadenium grantii latex

    Directory of Open Access Journals (Sweden)

    Larissa L. G. Costa

    2012-10-01

    Full Text Available Synadenium grantii Hook f., Euphorbiaceae, is popularly known as leitosinha or janaúba. The diluted latex (18 drops/L of water is commonly used in the south of Brazil to treat gastric disturbances. This study evaluated phytochemical screening and toxicity using Artemia salina Leach of crude bark extract and also latex. The toxicity and the anti-ulcer activity of S. grantii latex were also tested in rats. Phytochemical results showed presence of tannins, terpenes, unsaponificable substances, coumarins and anthraquinones in the crude bark extract and terpenes in the latex. Gas chromatography-mass spectrometry (GC-MS analysis demonstrated the presence of diterpene tigliane esters in the latex, identified as 12-deoxyphorbol-13-(2-metilpropionate and phorbol 12,13,20-triacetate. The toxicity results using A. salina presented CL50 26.58μg/mL and CL50 778.66μg/mL, for the latex and the crude bark extract respectively. The toxicological hepatic parameters of the diluted latex were not different to the control group (p<0.05. The eosinophils cells showed an increase in both the diluted and pure latex groups. The pure latex showed gastric protection of 90% (p<0.05 and the diluted latex showed 6% compared to the negative control. Therefore, our data indicate that S. grantii latex, under research conditions presented gastric protection. Pure latex showed more toxicity than the diluted latex.

  10. P(FA-co-MMA-co-St)共混改性环氧涂料的制备与疏水性能%Preparation and Hydrophotic Property of Copolymers P(FA-Co-MMA-co-St) Modified Epoxy Coatings

    Institute of Scientific and Technical Information of China (English)

    王月欣; 李景红; 张倩; 王善兴; 郝文珺

    2011-01-01

    The superhydrophobic epoxy coatings were prepared by adding the random copolymers poly-(fluoroalkyl ethyl acrylate-co-methly methacrylate-co-styrene) P(FA-co-MMA-co-St) to the commercially available epoxy paints using a simple blending method. The results indicated that when the copolymers are 4% of the epoxy components,perfluoroalkyl ethyl acrylate (FA) accounts for 30% of the comonomers, curing temperature is 120 ℃/2h, the water contact angle(WCA) of epoxy coatings is 152°, higher than 88° of unmodified epoxy coatings. Through scanning electron microscope(SEM), the microstructure was observed on the epoxy coatings. The low surface energy FA segrnents and the microstructure together renderes the modified epoxy coatings with superhydrophobic properties.The factors were studied as well.%采用简单的共混法,直接将聚全氟烷基乙基丙烯酸酯-co-甲基丙烯酸甲酯-co-苯乙烯无规共聚物P(FA-co-MMA-co-St)添加到市售的环氧涂料中,制备出具有超疏水性的环氧涂层.结果表明,当共聚物用量为环氧色漆组分的4%,氟单体投料量为30%,固化剂为乙二醇双偏苯三酸酐(TMEG)、固化温度120℃,固化时间2h条件下,改性环氧涂层对水的接触角可达152°,比纯的环氧涂层提高了88°.电子扫描显微镜观察发现,在环氧涂层表面构建出了具有微米级的粗糙结构.

  11. Structure and Mechanical Properties of Ethylene-butene Copolymers

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The crystallinity of ethylene-butene copolymers prepared by copolymerization of ethylene and butene in the presence of a new highly active catalyst was studied by means of DSC, WAXD and DMA. The results show that the melting temperature, the crystallinity and the crystallite size decreased with increasing the content of butene in the copolymers. The copolymers have a high degree of branching, the butene segments are mainly in the amorphous regions of the copolymers, while the polyethylene sequence forms crystal phase acting as crosslinking bondage between the molecules at room temperature. The ethylene-butene copolymers have a low modulus, a low stress and a high strain analogous to the stress-strain behavior of non-cross thermoplastic elastomer.

  12. Preparation and Characterization of Water-based Polyurethane/Gelatin Copolymers%水性聚氨酯/明胶共聚物的制备及表征

    Institute of Scientific and Technical Information of China (English)

    靳园敏; 王鸿儒

    2011-01-01

    以二羟甲基丙酸(DMPA)作为亲水单体,采用甲苯二异氰酸酯(TDI)、聚酯二元醇(PCDL)为原料,于水性介质中在偶联剂水杨醛的作用下,制备了聚氯酯/明胶共聚物,用傅里叶变换红外光谱(FTIR)分析及凝胶渗透色谱分析(GPC)证实了该共聚反应的发生;研究结果表明,DMPA质量分数为5%时,可得到稳定的聚氨酯乳液,此时胶膜的吸水率为8.52%;热重分析(TGA)显示,共聚物胶膜在240℃开始分解;示差扫描量热分析(DSC)显示,经改性后共聚物的玻璃化温度(Tg)为66 ℃;X射线衍射分析(XRD)表明,聚氨酯的加入使共聚物胶膜的结晶度大大降低,在聚氨酯质量分数为50%时,共聚物的结晶度降为2%;力学性能分析及耐水性测试表明,当聚氨酯质量分数从0%到50%变化时,胶膜的抗张强度由83 MPa下降到37.3 MPa,断裂伸长率从25.5%增大到325.6%,当聚氨酯质量分数从10%到50%变化时,胶膜的吸水率从251%下降到65%.%The present work presents a study on the grafting of polyurethane onto chitosan in aqueous media. The effect of the amount of hydrophilic monomer on the water resistance of polyurethane was observed. Characterization of graft copolymers was performed by fourier transform infrared spectroscopy ( FTIR ) , gel permeation chromatography ( GPC ) , thermogravimetric analysis ( TGA ) , differential scanning calorimetry( DSC) ,X-ray diffraction analysis( XRD) .mechanical properties testing,and water resistance testing. TGA tests reveal that the thermal decomposition temperature of the copolymers increased significantly, being 34 ℃ higher than that of pure gelatin, while DSC measurements indicate that the glass transition temperature decreased with the introduction of polyurethane. Accordingly, the mechanical and anti-water absorption properties also proved to be enhanced greatly as evidenced by mechanical test and water absorptions data in which the copolymers containing 50

  13. Thermoreversible copolymer gels for extracellular matrix.

    Science.gov (United States)

    Vernon, B; Kim, S W; Bae, Y H

    2000-07-01

    To improve the properties of a reversible synthetic extracellular matrix based on a thermally reversible polymer, copolymers of N-isopropylacrylamide and acrylic acid were prepared in benzene with varying contents of acrylic acid (0 to 3%) and the thermal properties were evaluated. The poly(N-isopropylacrylamide) and copolymers made with acrylic acid had molecular weights from 0.8 to 1.7 x10(6) D. Differential scanning calorimetry (DSC) showed the high-molecular-weight acrylic acid copolymers had similar onset temperatures to the homopolymers, but the peak width was considerably increased with increasing acrylic acid content. DSC and cloud point measurements showed that polymers with 0 to 3% acrylic acid exhibit a lower critical solution temperature (LCST) transition between 30 degrees and 37 degrees C. In swelling studies, the homopolymer showed significant syneresis at temperatures above 31 degrees C. Copolymers with 1 and 1.5% showed syneresis beginning at 32 degrees and 37 degrees C, respectively. At 37 degrees C the copolymers with 1.5-3% acrylic acid showed little or no syneresis. Due to the high water content and a transition near physiologic conditions (below 37 degrees C), the polymers with 1.5-2.0% acrylic acid exhibited properties that would be useful in the development of a refillable synthetic extracellular matrix. Such a matrix could be applied to several cell types, including islets of Langerhans, for a biohybrid artificial pancreas.

  14. 木粉-丙烯酰胺接枝共聚物的制备及其絮凝性能%Preparation and flocculation properties of graft copolymer from fir powder and acrylamide

    Institute of Scientific and Technical Information of China (English)

    郭立颖; 史铁钧

    2011-01-01

    首先用微波加热法(400 W,90℃)将杉木粉溶解在离子液体氯代1-(2-羟乙基)-3-乙基咪唑([HeEIM]Cl)中,再将溶解体系和丙烯酰胺(AM)原位共混,在过硫酸钾热引发条件下使溶解后的木粉和丙烯酰胺在离子液体介质中接枝共聚,制备了改性絮凝剂AM-g-wood,并用FTIR和XRD对其化学结构和结晶结构进行表征,比较研究离子液体和水分别作为反应介质对接枝共聚的影响,考察絮凝剂AM-g-wood对煤泥污水和陶土污水的絮凝效果.FTIR和XRD结果表明杉木粉与丙烯酰胺发生了接枝反应,其中以离子液体为介质制备的共聚物性能远远优于水介质,该絮凝剂对较细颗粒的陶土污水处理效果要优于煤泥污水,特别是在无机絮凝剂氯铝盐的协同作用下,絮凝效果更好.%Fir powder was dissolved in ionic liquid of 1-(2-hydroxylethyl)-3-ethyl imidazolium chloride ([HeEIM]Cl) by microwave heating (400 W, 90℃), then acrylamide (AM) was grafted onto the dissolved wood with initiator of K2S2O8 in the dissolution system to prepare the graft copolymer AM-g-wood, which was a novel modified flocculant. The chemical structure and crystalline structure of the flocculant were determined by FTIR and XRD respectively. The effects of ionic liquid and aqueous medium on graft copolymerization were studied. The flocculation properties of AM-g-wood on coal slurry water and argil wastewater were investigated. The results of FTIR and XRD showed that graft copolymerization occurred between AM and fir powder. The performance of AM-g-wood prepared in ionic liquid medium was far superior to that prepared in aqueous medium, and the graft copolymer was more suitable for treating argil wastewater with tiny particles. The effect of flocculation was better when inorganic flocculant of poly aluminum chloride (PAC) was used as synergistic agent.

  15. Synthesis and Characterization of a Biodegradable Copolymer: RGD Peptide Modification of Poly (lactic acid-co-lysine)

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    The poly ( lactic acid- co-lysine ) was synthesized using IR and 1 H NMR to characterize the copolymer. And then the RGD modification copolymer RGD-PLAL was prepared. The contact angles were used to see the RGD modification occurrence. Also high molecular weight polymer was controlled to the reaction of polymerization of copolymer.

  16. Preparation and Inhibition Performance of IA-HPEC Copolymer Scale Inhibitor%IA-HPEC共聚物阻垢剂的制备及阻垢性能

    Institute of Scientific and Technical Information of China (English)

    韶晖; 王雅; 周胤; 冷一欣; 钟璟

    2015-01-01

    以异丁烯醇聚氧乙烯醚(H PEG )、衣康酸(IA )为原料,在过硫酸铵-次亚磷酸钠引发剂作用下进行自由基共聚,合成阻垢剂IA-HPEC。采用FT-IR、1 H-NMR等方法表征IA-HPEC阻垢剂结构,采用扫描电镜(SEM )观察阻垢后形成的CaCO3晶体形貌。通过静态阻垢性能实验,考察了单体配比、聚合条件、氧化剂滴加方式及用量对合成的IA-HPEC阻垢剂阻垢性能的影响。结果表明,在 m(IA)/m(HPEC)=1、聚合温度110℃、聚合时间1.5 h、分批滴加氧化剂的最佳聚合条件下,合成的共聚物IA-HPEC对CaCO3的阻垢率为93.9%,优于市场含磷阻垢剂,具有较好的经济与环境效益。%IA-HPEC copolymer was synthesized with itaconic acid (IA ) and isobutylene alcohol ethoxylates (HPEG ) as raw material , ammonium persulfate-sodium hypophosphite as initiator . The product was characterized by FT-IR and 1 H-NMR .The influences of monomer mass ratio , polymerization conditions , oxidant dropping method and dosage on inhibition performance of synthesized IA-HPEC copolymer was investigated by the static scale inhibition experiment . The disordered CaCO3 crystal in the presence of IA-HPEC was analyzed by SEM .The results showed that the IA-HPEC synthesized under the optimal conditions of m (IA )/m ( HPEC ) = 1 , polymerization temperature 110℃ ,polymerization time 1.5 h and oxidant dropping in batches , exhibited excellent ability to control CaCO3 scale , when the inhibition rate on CaCO3 reached 93.9% .The scale inhibiting efficiency of IA-HPEC was better than market inhibitors ,indicating that IA-HPEC had good economic and environmental benefits .

  17. Safety of latex urinary catheters for the short time drainage

    Directory of Open Access Journals (Sweden)

    Mehrdad Hosseinpour

    2014-01-01

    Conclusion: It seems that urinary tract catheterization with latex catheters is a safe, feasible, and in-expensive procedure for short-term post-operative course in hypospadias surgery in patients without latex hypersensitivity.

  18. Morphological studies on block copolymer modified PA 6 blends

    Science.gov (United States)

    Poindl, M.; Bonten, C.

    2014-05-01

    Recent studies show that compounding polyamide 6 (PA 6) with a PA 6 polyether block copolymers made by reaction injection molding (RIM) or continuous anionic polymerization in a reactive extrusion process (REX) result in blends with high impact strength and high stiffness compared to conventional rubber blends. In this paper, different high impact PA 6 blends were prepared using a twin screw extruder. The different impact modifiers were an ethylene propylene copolymer, a PA PA 6 polyether block copolymer made by reaction injection molding and one made by reactive extrusion. To ensure good particle matrix bonding, the ethylene propylene copolymer was grafted with maleic anhydride (EPR-g-MA). Due to the molecular structure of the two block copolymers, a coupling agent was not necessary. The block copolymers are semi-crystalline and partially cross-linked in contrast to commonly used amorphous rubbers which are usually uncured. The combination of different analysis methods like atomic force microscopy (AFM), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) gave a detailed view in the structure of the blends. Due to the partial cross-linking, the particles of the block copolymers in the blends are not spherical like the ones of ethylene propylene copolymer. The differences in molecular structure, miscibility and grafting of the impact modifiers result in different mechanical properties and different blend morphologies.

  19. Morphological studies on block copolymer modified PA 6 blends

    Energy Technology Data Exchange (ETDEWEB)

    Poindl, M., E-mail: marcus.poindl@ikt.uni-stuttgart.de, E-mail: christian.bonten@ikt.uni-stuttgart.de; Bonten, C., E-mail: marcus.poindl@ikt.uni-stuttgart.de, E-mail: christian.bonten@ikt.uni-stuttgart.de [Institut für Kunststofftechnik, University of Stuttgart (Germany)

    2014-05-15

    Recent studies show that compounding polyamide 6 (PA 6) with a PA 6 polyether block copolymers made by reaction injection molding (RIM) or continuous anionic polymerization in a reactive extrusion process (REX) result in blends with high impact strength and high stiffness compared to conventional rubber blends. In this paper, different high impact PA 6 blends were prepared using a twin screw extruder. The different impact modifiers were an ethylene propylene copolymer, a PA PA 6 polyether block copolymer made by reaction injection molding and one made by reactive extrusion. To ensure good particle matrix bonding, the ethylene propylene copolymer was grafted with maleic anhydride (EPR-g-MA). Due to the molecular structure of the two block copolymers, a coupling agent was not necessary. The block copolymers are semi-crystalline and partially cross-linked in contrast to commonly used amorphous rubbers which are usually uncured. The combination of different analysis methods like atomic force microscopy (AFM), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) gave a detailed view in the structure of the blends. Due to the partial cross-linking, the particles of the block copolymers in the blends are not spherical like the ones of ethylene propylene copolymer. The differences in molecular structure, miscibility and grafting of the impact modifiers result in different mechanical properties and different blend morphologies.

  20. 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.

  1. Synthesis and characterization of butadiene-1,3 and octene-1 copolymer prepared by a Ziegler-Natta catalyst based on neodymium

    Directory of Open Access Journals (Sweden)

    Gustavo M. Silva

    2011-01-01

    Full Text Available The aim of this work is to evaluate the influence of octene-1 incorporation in the polybutadiene chain on the polymerization reaction and polymer characteristics. Thus, copolymerization of butadiene-1,3 with octene-1 using a Ziegler-Natta ternary catalyst based on neodymium was performed. The weight ratios of butadiene-1,3/α-olefin 100/0, 99/1, 97/3, 95/5, 90/10, 80/20 and 70/30 were evaluated. The copolymers were characterized by size exclusion chromatography (SEC, infrared spectroscopy (FTIR and thermogravimetric analysis (TG. The results showed that the degradation temperature (Tmax was not affected by the addition of alpha-olefin, while the thermal behavior has undergone significant changes. The polymer microstructure was not influenced by the increasing of octene-1 content. However, a tendency to molecular mass increase was observed with the increasing of octene-1 content. It was also observed a trend in reduction of the polymerization conversion as the octene-1 content increased.

  2. Electrochromic response of WO3 and WO3-TiO2 thin films prepared from water-soluble precursors and a block copolymer template

    Directory of Open Access Journals (Sweden)

    Takashi Kuroki

    2016-12-01

    Full Text Available Electrochromic tungsten trioxide (WO3 thin films are attracting renewed attention as transmittance-controllable windows for use in automobile, aircraft, and building applications. In order to achieve high electrochromic performance, high cycle stability, and high reliability, the microstructure and compositional homogeneity of WO3 thin films have to be optimized. In this study, non-doped WO3 and TiO2-doped WO3 thin films were fabricated from water-soluble precursors of tungsten and titanium, and their electrochromic response was investigated. Amorphous WO3 and TiO2-doped WO3 thin films were fabricated by calcining the spin-coated films at 573 K. The use of a PEO-PPO-PEO block copolymer as a porogen facilitated the redox reactions occurring on the thin film/electrolyte interface. Although the effect of TiO2-doping on the cycle stability of WO3 thin films has not been fully elucidated, this study demonstrated that TiO2 doping up to 15 mol% effectively enhanced the cycle stability.

  3. Preparation and characterization of L-lactide-silkworm chrysalis protein copolymer%L-丙交酯与蚕蛹蛋白共聚物的合成与表征

    Institute of Scientific and Technical Information of China (English)

    李仲昀; 文豪; 王冬; 李世云; 邹俊

    2014-01-01

    Poly(L-lactide-co-silkworm chrysalis protein)copolymer (PLLA-co-SCP)was prepared by melt con-densation polymerization of L-lactide with silkworm chrysalis protein.Stannous octoate (Sn(Oct)2 )was used as a catalyst.The influence of the reactant ratio on the intrinsic viscosity of the products was studied.The intrinsic viscosity results revealed that the largest intrinsic viscosity was 0.244 6 dL/g when the reactant ratio mL-LA:mSCP was 34∶1 .Their chemical structure,thermal properties and crystal structure were confirmed by FTIR,TGA, DSC and XRD.The FTIR showed that the copolymer included both ester groups of PLLA segments and amide groups of SCP segments.The TGA analysis indicated that the lager intrinsic viscosity could improve the thermo-stability of the copolymer,and thermal decomposition residue of copolymers increased with increasing SCP con-tent.The results of XRD and the DSC suggested that the crystallization of PLLA-co-SCP was mainly caused by PLLA segments,and the longer PLLA segments were,the higher crystallinity and the better crystal the PLLA-co-SCP got.The XRD analysis confirmed that the crystal unit cells of PLLA-co-SCP contained both αand βcrystal form.%以L-丙交酯和蚕蛹蛋白为原料,在辛酸亚锡的催化作用下,采用熔融聚合法合成了聚乳酸和蚕蛹蛋白的共聚物(PLLA-co-SCP),研究了投料比对共聚物特性粘数的影响,结果表明:L-丙交酯与蚕蛹蛋白投料比为34∶1时得到特性粘数最大为0.2446 dL/g的共聚物.用傅里叶红外光谱(FTIR)、热重分析(TGA)、差示扫描量热法(DSC)和 X 射线衍射(XRD)对PLLA-co-SCP共聚物的结构、热性能及结晶性能进行了表征.FTIR谱图分析结果表明:合成的PLLA-co-SCP共聚酯兼具了PLLA链段的酯基和蚕蛹蛋白的酰胺基;TGA测试结果显示PLLA-co-SCP特性粘数越大热稳定性越高, SCP含量越高热分解残留率越大;DSC和XRD结果表明PLLA-co-SCP结晶主要

  4. NANOSTRUCTURES OF FUNCTIONAL BLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    Guojun Liu

    2000-01-01

    Nanostructure fabrication from block copolymers in my group normally involves polymer design, synthesis, selfassembly, selective domain crosslinking, and sometimes selective domain removal. Preparation of thin films with nanochannels was used to illustrate the strategy we took. In this particular case, a linear triblock copolymer polyisopreneblock-poly(2-cinnamoylethyl methacrylate)-block-poly(t-butyl acrylate), PI-b-PCEMA-b-PtBA, was used. Films, 25 to50μm thick, were prepared from casting on glass slides a toluene solution of PI-b-PCEMA-b-PtBA and PtBA homopolymer,hPtBA, where hPtBA is shorter than the PtBA block. At the hPtBA mass fraction of 20% relative to the triblock or the total PtBA (hPtBA and PtBA block) volume fraction of 0.44, hPtBA and PtBA formed a seemingly continuous phase in the matrix of PCEMA and PI. Such a block segregation pattern was locked in by photocrosslinking the PCEMA domain. Nanochannels were formed by extracting out hPtBA with solvent. Alternatively, larger channels were obtained from extracting out hPtBA and hydrolyzing the t-butyl groups of the PtBA block. Such membranes were not liquid permeable but had gas permeability constants ~6 orders of magnitude higher than that of low-density polyethylene films.

  5. [Latex agglutination test in amebic liver abscess].

    Science.gov (United States)

    Gómez Maganda y Silva, T; García Carrizosa, R; Torres Valadez, F; Ortiz Ramírez, E; Villaseñor de la Parra, C; Flores González, A; Gómez García, E

    1978-01-01

    Amebic hepatic abscesses are one of the most frequent and serious complications of intestinal amibiasis. Although many methods exists with which the diagnosis can be made, frequently problems do arise. Serologic reactions play an important role in the diagnosis of amebic hepatic abscess. Among the most useful of the serological tests, is that which evaluates agglutination with latex particles. Latex agglutination was positive in 98.5% of 200 cases of proved amebic hepatic abscess. The pros and cons of the utility of this test compared with other serological tests are discussed. It is concluded that or the especialist as well as the general practicioner latex agglutination can be extremely useful in the diagnosis of amebic hepatic abscess.

  6. Angiogenic activity of Synadenium umbellatum Pax latex

    Directory of Open Access Journals (Sweden)

    PR. Melo-Reis

    Full Text Available Synadenium umbellatum Pax, popularly known as "cola-nota", is a medicinal plant that grows in tropical regions. Latex of this plant is used to treat various diseases such as diabetes mellitus, Hansen´s disease, tripanosomiases, leukemia and several malignant tumors. In the present study, the angiogenic activity of S. umbellatum latex was evaluated using the chick embryo chorioallantoic membrane (CAM assay. Results showed significant increase of the vascular net (p < 0.05 compared to the negative control (H2O. The histological analysis was in accordance with the results obtained. In conclusion, our data indicate that S. umbellatum latex, under the conditions of this research, presented angiogenic effect.

  7. CHARACTERIZATION AND RECYCLING OF WASTE WATER FROM GUAYULE LATEX EXTRACTION

    Science.gov (United States)

    Guayule commercialization for latex production to be used in medical products and other applications is now a reality. Currently, waste water following latex extraction is discharged into evaporation ponds. As commercialization reaches full scale, the liquid waste stream from latex extraction will b...

  8. Function of fibrinogen gamma-chain dodecapeptide-conjugated latex beads under flow.

    Science.gov (United States)

    Takeoka, Shinji; Okamura, Yosuke; Teramura, Yuji; Watanabe, Naohide; Suzuki, Hidenori; Tsuchida, Eishun; Handa, Makoto; Ikeda, Yasuo

    2003-12-19

    In order to perform a fundamental study of platelet substitutes, novel particles that bound to activated platelets were prepared using two oligopeptides conjugated to latex beads. The oligopeptides were CHHLGGAKQAGDV (H12), which is a fibrinogen gamma-chain carboxy-terminal sequence (gamma 400-411), and CGGRGDF (RGD), which contains a fibrinogen alpha-chain sequence (alpha 95-98 RGDF). Both peptides contained an additional amino-terminal cysteine to enable conjugation. Human serum albumin was adsorbed onto the surface of latex beads (average diameter 1microm) and pyridyldisulfide groups were chemically introduced into the adsorbed protein. H12 or RGD peptides were then chemically linked to the modified surface protein via disulfide linkages. H12- or RGD-conjugated latex beads prepared in this way enhanced the in vitro thrombus formation of activated platelets on collagen-immobilized plates under flowing thrombocytopenic-imitation blood. Based on the result of flow cytometric analyses of agglutination, PAC-1 binding, antiP-selectin antibody binding, and annexin V binding, the H12-conjugated latex beads showed minimal interaction with non-activated platelets. These results indicate the excellent potential of H12-conjugated particles as a candidate for a platelet substitute.

  9. Preparation of Canna edulis Ker Starch-Acrylic Acid Graft Copolymer by Inverse Microemulsion Method%反相微乳液法制备芭蕉芋淀粉接枝丙烯酸盐共聚物

    Institute of Scientific and Technical Information of China (English)

    顾千辉; 黄赣辉; 顾振宇

    2011-01-01

    Canna edulis Ker starch-acrylic acid graft copolymer was prepared by an inverse microemulsion method using ammonium persulfate as the initiator and N,N'-meyhylene-bisacrylamide as cross-linking agent under nitrogen protection.An inverse emulsion system containing Canna edulis Ker starch was formed under an oil-to-water ratio of 1.2:1,complex emulsifier amount of 30%,and emulsifier HLB(hydrophilic-lipophilic balance) of 7.36.The optimal copolymerization conditions of Canna edulis Ker starch and acrylic acid were acrylic acid amount of 16 mL,initiator amount of 3.5%,cross-linking agent amount of 0.8%,and neutralization degree of acrylic acid of 70%.The water-absorbing capacity of graft copolymers prepared under the optimal conditions was 1340 g/g.Meanwhile,infrared spectral analysis revealed that acrylic acid was successfully grafted onto Canna edulis Ker starch.%在氮气保护的环境下,以过硫酸铵为引发剂、N,N'-亚甲基双丙烯酰胺为交联剂,采用反相微乳液法制备芭蕉芋淀粉接枝丙烯酸盐共聚物;确定含芭蕉芋淀粉的稳定反相微乳液体系的制备工艺:油水比为1.2:1、复合乳化剂用量为30%、乳化剂的亲水亲油平衡值(hydrophile lipophylic balance,HLB)为7.36;利用正交试验法优化利用反相微乳液法制备淀粉接枝丙烯酸盐共聚物的工艺条件,在最佳工艺(单体丙烯酸的用量16mL、引发剂用量3.5%、交联剂用量0.8%、单体丙烯酸中和度70%)条件下,制备出芭蕉芋淀粉接枝丙烯酸盐共聚物的吸水倍率可达1340g/g。红外光谱分析结果表明,聚合过程中芭蕉芋淀粉与丙烯酸发生了接枝共聚反应。

  10. Nanopatterned articles produced using surface-reconstructed block copolymer films

    Energy Technology Data Exchange (ETDEWEB)

    Russell, Thomas P.; Park, Soojin; Wang, Jia-Yu; Kim, Bokyung

    2016-06-07

    Nanopatterned surfaces are prepared by a method that includes forming a block copolymer film on a substrate, annealing and surface reconstructing the block copolymer film to create an array of cylindrical voids, depositing a metal on the surface-reconstructed block copolymer film, and heating the metal-coated block copolymer film to redistribute at least some of the metal into the cylindrical voids. When very thin metal layers and low heating temperatures are used, metal nanodots can be formed. When thicker metal layers and higher heating temperatures are used, the resulting metal structure includes nanoring-shaped voids. The nanopatterned surfaces can be transferred to the underlying substrates via etching, or used to prepare nanodot- or nanoring-decorated substrate surfaces.

  11. Nanopatterned articles produced using reconstructed block copolymer films

    Energy Technology Data Exchange (ETDEWEB)

    Russell, Thomas P.; Park, Soojin; Wang; , Jia-Yu; Kim, Bokyung

    2017-05-02

    Nanopatterned surfaces are prepared by a method that includes forming a block copolymer film on a substrate, annealing and surface reconstructing the block copolymer film to create an array of cylindrical voids, depositing a metal on the surface-reconstructed block copolymer film, and heating the metal-coated block copolymer film to redistribute at least some of the metal into the cylindrical voids. When very thin metal layers and low heating temperatures are used, metal nanodots can be formed. When thicker metal layers and higher heating temperatures are used, the resulting metal structure includes nanoring-shaped voids. The nanopatterned surfaces can be transferred to the underlying substrates via etching, or used to prepare nanodot- or nanoring-decorated substrate surfaces.

  12. [Cicatrization effect of Jatropha curcas latex (Angiospermae: Euforbiaceae)].

    Science.gov (United States)

    Salas, J; Tello, V; Zavaleta, A; Villegas, L; Salas, M; Fernández, I; Vaisberg, A

    1994-01-01

    The wound healing effects of Jathopha curcas latex upon surgical wound produced in Balb/c mice skin, were studied with a modification of the Hoowes-Sooy-Harvey method. The effects of topical treatment using single 50 ul doses of latex at different dilutions (10% to 100%) was compared with a multiple dose treatment (four 25 ul/dose q12h, latex 5% to 100%). The single dose treatment with 10%, 50% or 100% latex and the multiple dose treatment with dilutions between 5% and 10%, have a healing effect but only on males. The multiple dose treatment with 50% or pure undiluted latex produced caustic lesions to treated skin.

  13. Thin Film Assembly of Spider Silk-like Block Copolymers

    Science.gov (United States)

    2011-01-01

    Film Assembly of Spider Silk -like Block Copolymers Sreevidhya T. Krishnaji,†,‡ Wenwen Huang,§ Olena Rabotyagova,†,‡ Eugenia Kharlampieva, ) Ikjun Choi...Received November 26, 2010 We report the self-assembly of monolayers of spider silk -like block copolymers. Langmuir isotherms were obtained for a series of...bioengineered variants of the spider silks , and stable monolayers were generated. Langmuir-Blodgett films were prepared by transferring the monolayers

  14. Case report of latex aerosolization from a transesophageal echocardiogram machine.

    Science.gov (United States)

    Muller, Barbara A; Steelman, Victoria J

    2004-01-01

    Aerosolized natural rubber latex proteins produce latex sensitization and can cause acute allergic reactions in susceptible individuals. The objective of this study is to describe measures that should be taken to ensure a latex-safe hospital environment. A case of latex-induced anaphylaxis prompted a survey of air quality in acute care areas of a major tertiary health care center that had eliminated the use of powder-free latex gloves years earlier. Six air samples were collected using pre- and postcalibrated sampling pumps operating at 2.7 L/minute. Samples were collected in duplicate on three-piece 37-mm Teflon filters in open-faced cassettes and tested for latex allergen by inhibition immunoassay. All samples had less than the detection limit > 5 ng/m3 for aerosolized latex except for the echocardiogram suite where the transesophageal echocardiogram machine was located. After thorough cleaning of the suite and echocardiogram machine, subsequent air sampling showed no detectable latex aerosolization particles. Follow-up investigation to discover the source of contamination revealed that the department performing routine maintenance on the echocardiogram equipment used powdered latex gloves obtained outside the hospital. Employees who are latex allergic may experience symptoms even in an environment of powder-free, nonlatex gloves. The site was a contaminated transesophageal echocardiogram machine. Institutional policies should be in place to monitor employee complaints and address allergic reactions to latex.

  15. Application of recombinant latex allergens in diagnostics of occupational latex allergy

    Directory of Open Access Journals (Sweden)

    Ewa Nowakowska-Świrta

    2015-02-01

    Full Text Available Over many years, allergy to natural rubber latex has been a major problem among health care workers (HCW. The diagnosis of occupational allergy requires methods of high diagnostic accuracy in view of certification implications (e.g., a sick worker quits a job. With the development of molecular methods, the frequency of application of recombinant allergens in the diagnostics of allergic diseases continues to increase. This paper reviews the applicability of laboratory tests which use recombinant allergens in the diagnostics of occupational allergy. The diagnosis of latex allergy is based on the presence of clinical symptoms linked with exposure to latex allergens, positive skin prick tests and detection of specific IgE antibodies to latex in serum. Moreover, in some cases specific challenge tests are conducted. The analysis of literature indicates that applying the panel of recombinant latex allergens in diagnostic tests, cross-reactivity can very likely be excluded and/or sensitization can be confirmed without the need for specific challenge tests, which in case of latex allergens carries a potential risk of generalized reactions. Med Pr 2015;66(1:85–97

  16. Latex allergy in dentistry: clinical cases report

    NARCIS (Netherlands)

    Raggio, D.P.; Camargo, L.B.; Naspitz, G.M.C.C.; Politano, G.T.; Bonifacio, C.C.; Mendes, F.M.; Kierstman, F.

    2010-01-01

    Generally natural rubber latex (NRL) allergy is detected after some exposition to the material. As NRL is commonly found in different materials used daily in dental clinic, the allergy can be manifested in the pediatric dentistry clinic. The first clinical manifestation can be smooth but also severe

  17. Latex allergy in dentistry: clinical cases report

    NARCIS (Netherlands)

    Raggio, D.P.; Camargo, L.B.; Naspitz, G.M.C.C.; Politano, G.T.; Bonifacio, C.C.; Mendes, F.M.; Kierstman, F.

    2010-01-01

    Generally natural rubber latex (NRL) allergy is detected after some exposition to the material. As NRL is commonly found in different materials used daily in dental clinic, the allergy can be manifested in the pediatric dentistry clinic. The first clinical manifestation can be smooth but also

  18. Synthesis and Characterization of Poly(St-co-BA) Latex with an Organic-Inorganic Hybrid Compound as Emulsifier

    Institute of Scientific and Technical Information of China (English)

    袁俊杰; 周树学; 廖建和; 武利民

    2003-01-01

    A poly (St-co-BA) latex was successfully synthesized by using an organic-inorganic hybrid compound (OIHC), an aliphatic carboxylate sodium/nano-silica composite, as the emulsifier, and investigated by particle size analyzer, transmission electron microscope (TEM), optical contact angle measurement (OCA) and dynamic mechanical analyzer (DMA). It was found that the protective agent, sodium polyacrylate (PA),could obviously improve the polymerization stability and the functional monomer, glycidyl methacrylate (GMA), could enhance the store stability of the latex. The particle size of poly(St-co-BA) latex decreased and then leveled off as OIHC content increased. TEM shows that the prepared polymers were a~:tually organic-inorganic nanocomposites, and these films have better waterproof property than those prepared by traditional poly(St-co-BA) latex or organic silicone modified poly(St-co-BA) latex. The nanocomposite polymer has much higher glass transition temperature than organic silicone modified poly(St-co-BA) polymer containing the same organic silicone content.

  19. Triterpenoid biosynthesis in Euphorbia lathyris latex

    Energy Technology Data Exchange (ETDEWEB)

    Hawkins, D.R.

    1987-11-01

    The structures of triterpenols, not previously been known, from Euphorbia lathyris latex are reported. A method for quantifying very small amounts of these compounds was developed. Concerning the biochemistry of the latex, no exogenous cofactors were required for the biosynthesis and the addition of compounds such as NADPAH and ATP do not stimulate the biosynthesis. The addition of DTE or a similar anti-oxidant was found to help reduce the oxidation of the latex, thus increasing the length of time that the latex remains active. The requirement of a divalent cation and the preference for Mn in the pellet was observed. The effect of several inhibitors on the biosynthesis of the triterpenoids was examined. Mevinolin was found to inhibit the biosynthesis of the triterpenoids from acetate, but not mevalonate. A dixon plot of the inhibition of acetate incorporation showed an I/sub 50/ concentration of 3.2 ..mu..M. Fenpropimorph was found to have little or no effect on the biosynthesis. Tridemorph was found to inhibit the biosynthesis of all of the triterpenoids with an I/sub 50/ of 4 ..mu..M. It was also observed that the cyclopropyl containing triterpenols, cycloartenol and 24-methylenecycloartenol were inhibited much more strongly than those containing an 8-9 double bond, lanosterol and 24-methylenelanosterol. The evidence indicates, but does not definetely prove, that lanosterol and 24-methylenelanosterol are not made from cycloartenol and 24-methylenecycloartenol via a ring-opening enzyme such as cycloeucalenol-obtusifoliol isomerase. The possibilty that cycloartenol is made via lanosterol was investigated by synthesizing 4-R-4-/sup 3/H-mevalonic acid and incubating latex with a mixture of this and /sup 14/C-mevalonic acid. From the /sup 3/H//sup 14/C ratio it was shown that cycloartenol and 24-methylenecycloartenol are not made via an intermediate containing as 8-9 double bond. 88 refs., 15 figs., 30 tabs.

  20. Triterpenoid biosynthesis in Euphorbia lathyris latex

    Energy Technology Data Exchange (ETDEWEB)

    Hawkins, D.R.

    1987-11-01

    The structures of triterpenols, not previously been known, from Euphorbia lathyris latex are reported. A method for quantifying very small amounts of these compounds was developed. Concerning the biochemistry of the latex, no exogenous cofactors were required for the biosynthesis and the addition of compounds such as NADPAH and ATP do not stimulate the biosynthesis. The addition of DTE or a similar anti-oxidant was found to help reduce the oxidation of the latex, thus increasing the length of time that the latex remains active. The requirement of a divalent cation and the preference for Mn in the pellet was observed. The effect of several inhibitors on the biosynthesis of the triterpenoids was examined. Mevinolin was found to inhibit the biosynthesis of the triterpenoids from acetate, but not mevalonate. A dixon plot of the inhibition of acetate incorporation showed an I/sub 50/ concentration of 3.2 ..mu..M. Fenpropimorph was found to have little or no effect on the biosynthesis. Tridemorph was found to inhibit the biosynthesis of all of the triterpenoids with an I/sub 50/ of 4 ..mu..M. It was also observed that the cyclopropyl containing triterpenols, cycloartenol and 24-methylenecycloartenol were inhibited much more strongly than those containing an 8-9 double bond, lanosterol and 24-methylenelanosterol. The evidence indicates, but does not definetely prove, that lanosterol and 24-methylenelanosterol are not made from cycloartenol and 24-methylenecycloartenol via a ring-opening enzyme such as cycloeucalenol-obtusifoliol isomerase. The possibilty that cycloartenol is made via lanosterol was investigated by synthesizing 4-R-4-/sup 3/H-mevalonic acid and incubating latex with a mixture of this and /sup 14/C-mevalonic acid. From the /sup 3/H//sup 14/C ratio it was shown that cycloartenol and 24-methylenecycloartenol are not made via an intermediate containing as 8-9 double bond. 88 refs., 15 figs., 30 tabs.

  1. Hybrid, Nanoscale Phospholipid/Block Copolymer Vesicles

    Directory of Open Access Journals (Sweden)

    Bo Liedberg

    2013-09-01

    Full Text Available Hybrid phospholipid/block copolymer vesicles, in which the polymeric membrane is blended with phospholipids, display interesting self-assembly behavior, incorporating the robustness and chemical versatility of polymersomes with the softness and biocompatibility of liposomes. Such structures can be conveniently characterized by preparing giant unilamellar vesicles (GUVs via electroformation. Here, we are interested in exploring the self-assembly and properties of the analogous nanoscale hybrid vesicles (ca. 100 nm in diameter of the same composition prepared by film-hydration and extrusion. We show that the self-assembly and content-release behavior of nanoscale polybutadiene-b-poly(ethylene oxide (PB-PEO/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylcholine (POPC hybrid phospholipid/block copolymer vesicles can be tuned by the mixing ratio of the amphiphiles. In brief, these hybrids may provide alternative tools for drug delivery purposes and molecular imaging/sensing applications and clearly open up new avenues for further investigation.

  2. Synthesis of polymer latex particles decorated with organically-modified laponite clay platelets via emulsion polymerization.

    Science.gov (United States)

    Herrera, Norma Negrete; Persoz, Stéphanie; Putaux, Jean-Luc; David, Laurent; Bourgeat-Lami, Elodie

    2006-02-01

    We report a new route to colloidal nanocomposites consisting of polymer latex particles covered with Laponite clay nanoplatelets. These composite particles are prepared by seeded emulsion (co)polymerization of styrene and butyl acrylate from Laponite clay suspensions previously functionalized by ion exchange using either a free radical initiator: 2,2-azobis (2-methylpropionamidine) hydrochloride (AIBA) or a cationic vinyl monomer: 2-(methacryloyloxy) ethyl trimethyl ammonium chloride (MADQUAT). The successful intercalation of the cationic reactive molecules was confirmed by elemental analysis, FTIR, 13C solid-state NMR and WAXD. The organically-modified clays were dispersed into water with the help of tetrasodium pyrophosphate and an anionic surfactant. stable latexes, produced under different experimental conditions, were successfully obtained from the clay suspensions. Cryo-TEM images of the resulting latexes showed spherical composite particles with diameters in the 50-250 nm range with clay sheets located on their surface. This paper reports on the effect of the processing conditions on the particle morphology and latex stability, and describes the mechanism of formation of the nanocomposite particles.

  3. Bimodal Latex Effect on Spin-Coated Thin Conductive Polymer-Single-Walled Carbon Nanotube Layers.

    Science.gov (United States)

    Moradi, Mohammad-Amin; Larrakoetxea Angoitia, Katalin; van Berkel, Stefan; Gnanasekaran, Karthikeyan; Friedrich, Heiner; Heuts, Johan P A; van der Schoot, Paul; van Herk, Alex M

    2015-11-10

    We synthesize two differently sized poly(methyl methacrylate-co-tert-butyl acrylate) latexes by emulsion polymerization and mix these with a sonicated single-walled carbon nanotube (SWCNT) dispersion, in order to prepare 3% SWCNT composite mixtures. We spin-coat these mixtures at various spin-speed rates and spin times over a glass substrate, producing a thin, transparent, solid, conductive layer. Keeping the amount of SWCNTs constant, we vary the weight fraction of our smaller 30-nm latex particles relative to the larger 70-nm-sized ones. We find a maximum in the electrical conductivity up to 370 S/m as a function of the weight fraction of smaller particles, depending on the overall solid content, the spin speed, and the spin time. This maximum occurs at 3-5% of the smaller latex particles. We also find a more than 2-fold increase in conductivity parallel to the radius of spin-coating than perpendicular to it. Atomic force microscopy points at the existence of lanes of latex particles in the spin-coated thin layer, while large-area transmission electron microscopy demonstrates that the SWCNTs are aligned over a grid fixed on the glass substrate during the spin-coating process. We extract the conductivity distribution on the surface of the thin film and translate this into the direction of the SWCNTs in it.

  4. Radiation prevulcanized natural rubber latex: Cytotoxicity and safety evaluation on animal

    Science.gov (United States)

    Keong, C. C.; Zin, W. M. Wan; Ibrahim, P.; Ibrahim, S.

    2010-05-01

    Radiation prevulcanized natural rubber latex (RVNRL) was claimed to be more user friendly than natural rubber latex prevulcanized by sulphur curing system. The absence of Type IV allergy inducing chemicals in RVNRL make it a suitable material for manufacturing of many kinds of latex products, especially those come into direct contact with users. This paper reveals and discusses the findings of cytotoxicity test and safety evaluation on animal for RVNRL. The test was done on RVNRL films prepared by coagulant dipping method and RVNRL dipped products produced by latex dipped product manufacturers. Cytotocixity test was carried out on mammalian cell culture American Type Culture Collection CCL 81, Vero. Results indicated that no cytotoxic effect from RVNRL films and products was found on the cell culture. Two animal studies, namely dermal sensitization study and primary skin irritation study, were done on gloves made from RVNRL. Albino white guinea pigs were used as test subjects in dermal sensitization study and results showed no sensitization induced by the application of test material in the guinea pigs. Primary skin irritation study was done on New Zealand white rabbits and results showed that the product tested was not corrosive and was not a primary irritant

  5. Permeability of nitrile rubber, latex, polyurethane, and neoprene gloves to 18 antineoplastic drugs.

    Science.gov (United States)

    Connor, T H

    1999-12-01

    The permeability of four glove materials to various antineoplastic drugs was studied. Eighteen antineoplastic drugs posing potential health hazards to handlers were prepared at the highest concentrations normally encountered by hospital personnel. Four glove materials-nitrile rubber, latex, polyurethane, and neoprene-were exposed to the drugs for 30, 60, 90, and 120 minutes. Glove thickness was measured with an electronic digital caliper. Random samples of material were selected from the glove fingertips, and triplicate samples were tested for each drug at each interval. For a majority of the drugs, a bacterial mutagenicity assay was used to measure the amount of drug (if any) that permeated the material. High-performance liquid chromatography was used for drugs not tested with the bacterial assay. The nitrile gloves were the thinnest (0.12 mm), and the latex gloves were the thickest (0.18 mm). The four materials were generally impermeable to each drug. One sample of the nitrile gloves appeared to have a defect, allowing >5% of the drug solution to pass through at 30 minutes. One sample each of the latex, polyurethane, and neoprene gloves demonstrated minimal permeability (neoprene materials. Nitrile rubber, latex, polyurethane, and neoprene gloves were impermeable to 18 antineoplastic drugs in most, but not all, cases.

  6. Radiation prevulcanized natural rubber latex: Cytotoxicity and safety evaluation on animal

    Energy Technology Data Exchange (ETDEWEB)

    Keong, C C; Zin, W M Wan; Ibrahim, P; Ibrahim, S, E-mail: chai@nuclearmalaysia.gov.my [Malaysian Nuclear Agency, Bangi, 43000 Kajang, Selangor (Malaysia)

    2010-05-15

    Radiation prevulcanized natural rubber latex (RVNRL) was claimed to be more user friendly than natural rubber latex prevulcanized by sulphur curing system. The absence of Type IV allergy inducing chemicals in RVNRL make it a suitable material for manufacturing of many kinds of latex products, especially those come into direct contact with users. This paper reveals and discusses the findings of cytotoxicity test and safety evaluation on animal for RVNRL. The test was done on RVNRL films prepared by coagulant dipping method and RVNRL dipped products produced by latex dipped product manufacturers. Cytotocixity test was carried out on mammalian cell culture American Type Culture Collection CCL 81, Vero. Results indicated that no cytotoxic effect from RVNRL films and products was found on the cell culture. Two animal studies, namely dermal sensitization study and primary skin irritation study, were done on gloves made from RVNRL. Albino white guinea pigs were used as test subjects in dermal sensitization study and results showed no sensitization induced by the application of test material in the guinea pigs. Primary skin irritation study was done on New Zealand white rabbits and results showed that the product tested was not corrosive and was not a primary irritant

  7. Preparation and Dielectric Properties of a-MWNTs/Poly ( metal phthalocyanine) imide Copolymers%聚(金属酞菁)酰亚胺/碳纳米管复合材料的制备及介电性能

    Institute of Scientific and Technical Information of China (English)

    张丽梅; 王琦桐; 杨旭; 姜振华; 张云鹤

    2012-01-01

    以四氨基铜(锌)酞菁为四胺单体,与4,4'-二苯醚二胺(4,4'-ODA)和二苯醚四酸酐(ODPA)进行共聚,合成了聚(金属酞菁)酰亚胺.由于金属酞菁的引入,聚(铜酞菁)酰亚胺和聚(锌酞菁)酰亚胺的介电常数均高于传统聚酰亚胺(PI).以聚(铜酞菁)酰亚胺为基体,采用溶液共混的方法,制备了一系列碳纳米管/聚(铜酞菁)酰亚胺复合材料,碳纳米管较为均匀地分散在聚合物基体中.复合材料具有良好的介电性能,掺杂碳纳米管质量分数为20%的复合材料的介电常数达到200,介电损耗为2.25.%Poly (metal phthalocyanine) imide copolymers [P(MPc)I] were prepared with tetra-phthalocya-nine teraamines(4NH2-MPc) , 4,4'-diamino diphenyl ether(4,4'-ODA) , and 4,4'-oxydiphthalic anhydride (ODPA). The dielectric constants of the polymer are higher than traonditional polyimide(PI). Carbon nano-tubes/poly(copper phthalocyanine)imide [a-MWNTs/P(CuPc)I] composites with different contents of carbon nanotubes were prepared using solution method. Carbon nanotubes show good dispersion in P(CuPc)I matrix. The composite containing 20% carbon nanotubes have high dielectric constant of ca. 200 and low dielectric loss of ca. 2. 25(at 1 kHz) which show good dielectric properties.

  8. Synthesis of Graft Copolymer of Natural Rubber by ATRP Ⅲ.Preparation of NR-g-PMMA%采用ATRP合成天然橡胶接枝共聚物——Ⅲ.NR-g-PMMA的制备

    Institute of Scientific and Technical Information of China (English)

    赵伟; 廖建和; 廖禄生; 杨耀华; 黄仙红; 陈永平

    2012-01-01

    An atom transfer radical polymerization(ATRP) macroinitiator, bromo-(natural rubber) [NR-Br(l) ], was synthesized by the reaction of natural rubber (NR) with N-bromosuccinimide. A novel graft copolymer, (natural rubber)-g-poly( methyl methacrylate) [NR-g-PMMA(2) ] , was prepared from methyl methacrylate (MMA) using 1 as a macroinitiator and CuBr/PMDTA as the catalyst by ATRP. The structures were characterized by !H NMR and IR. The results of preliminary study of graft copolymerization dynamics showed that the reaction of NR with NBS at high temperature easily occurred addition and cyclization, 1 prepared at room temperature exhibited higher initiating activity, and the graft copolymerization accorded with first-order kinetic reaction because the molecular weight of 2 increaseed as MMA monomer conversion increases.%N-溴代丁二酰亚胺与天然橡胶(NR)反应合成了大分子引发剂——溴代天然橡胶[NR-Br(1)].通过原子转移自由基聚合(ATRP),以CuBr/PMDTA为催化体系,1引发甲基丙烯酸甲酯(MMA)接枝共聚制得新型天然橡胶-g-聚甲基丙烯酸甲酯[NR-g-PMMA(2)],其结构经1H NMR和IR表征.初步聚合反应动力学研究结果表明,NBS与NR在高温下反应容易伴随双键加成和环化反应,于室温反应所得1具有较高的引发活性;接枝聚合符合一级动力学反应,即2的分子量随MMA单体转化率的提高而增加.

  9. 淀粉丙烯腈接枝共聚物皂化制备吸水剂%The Preparation Technology of Water-Absorbent by the Saponification of the Graft Copolymer of Starch and Acrylonitrile

    Institute of Scientific and Technical Information of China (English)

    顾正彪; 吴嘉根

    2001-01-01

    通过对淀粉丙烯腈接枝共聚物(SPAN)皂化制备吸水剂HSPAN的研究表明:HSPAN为水不溶性凝胶,但具有很强的吸水能力.以氢氧化钾皂化,酸作沉淀剂,经洗涤、分散和干燥制备HSPAN的工艺路线较为理想.皂化工艺条件在用碱量为SPAN中接枝链部分摩尔数的1.1倍、皂化温度95°C以上、皂化时间大于3h,且HSPAN的平板干燥温度在70°C时最好.当SPAN接枝百分率在70%左右时,制得的HSPAN吸水率最高.%Studies on the Preparation Technology of Water-absorbent (HSPAN)by the Saponification of the graft Copolymer of Starch and Acrylonitrile (SPAN) showed that, HSPAN was a kind of gel which was insoluble in water but could absorb a great amount of water. The best technology for the preparation of HSPAN was that,after SPAN was saponified by potassium hydroxide, precipited by sulfuric acid, washed and dispersed in water again, HSPAN was obtained by drying it on a plate. Moreover, the best conditions were that,the quantity of potassium hydroxide used in saponification was 1.1 as much as the mole of polyacrylonitrile in SPAN, saponifying temperature over 95°C, reaction time more than 3 h and drying temperature at 70°C. In addition, the highest water-absorbing capacity could be obtained from the SPAN in which grafted ratio was 70% or so.

  10. Effects of EVA Latex on the Properties of Glass-fiber/ Magnesium-oxychloride Cement Composites

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The effects of Ethylene- Vinyl Acetate copolymer ( EVA ) latex as an additive or a glass fiber sur face modifier on the properties of Glass- Fiber ( GF ) / Magnesium Oxychloride Cement ( MOC ) composites was studied.The mechanical properties, water resistance and aging resistance of the cured GF/ MOC composites were estimated and chemical ingredients analysis and morphological study of the GF/ MOC composites were also performed.It is found that EVA added to the MOC matrix could substantially improve the interfacial adhesion, water resistance and aging resistance of GF / MOC composites.EVA treatment on glass fibers resulted in decreasing initial flexural strength of GF/ MOC composites while enhancing the soft coefficients.In addition, the drying time and dilution of the EVA treatment on glass fibers also had an obvious effect on the properties of GF/ MOC composites.GF / MOC composites.

  11. Morphology diagram of a diblock copolymer - aluminosilicate nanoparticle system

    NARCIS (Netherlands)

    Garcia, B.C.; Kamperman, M.M.G.; Ulrich, R.; Jain, A.; Gruner, S.M.; Wiesner, U.

    2009-01-01

    We explore the morphology space of nanocomposites prepared from poly(isoprene-block-ethylene oxide) (PI-b-PEO) diblock copolymers as structure directing agents for aluminosilicate nanoparticles prepared from (3-glycidyloxypropyl)trimethoxysilane (GLYMO) and aluminum(III) sec-butoxide. The results of

  12. Medical devices manufactured from latex: European regulatory initiatives.

    Science.gov (United States)

    De Jong, W H; Geertsma, R E; Tinkler, J J B

    2002-05-01

    In Europe the marketing of medical devices manufactured from latex is regulated by directives describing the essential (safety) requirements that products have to fulfill to obtain marketing approval. This paper describes the general requirements for marketing medical devices in Europe and, more specifically, the requirements for products manufactured from natural rubber latex. The requirements for marketing medical devices can be fulfilled by using the relevant harmonized European standards. These standards are regularly under revision to incorporate the latest scientific developments. For certain devices, for example, latex medical (examination and surgical) gloves, specific standards have been published. Medical devices manufactured from latex pose a serious problem because of the risk of induction of allergy both against the latex proteins inherently present (type I or immediate type allergy) and against chemicals added during processing (type IV or delayed type hypersensitivity) present as residues in the latex products. So, besides requirements for product quality in terms of barrier properties, strength, and sterility, the main focus consists of the allergy-inducing properties of the latex products. Recent developments have reopened the discussion on the value of total protein versus allergen determination in latex medical gloves. However, as long as minimal levels needed for both sensitization and elicitation have not been established, a safe maximum level for leachable proteins/allergens in latex products cannot be determined. A European Commission guidance document on the latex allergy problem is currently being drafted by experts from Competent Authorities.

  13. ADVERSE REACTION TO LATEX CONTAINING MATERIALS IN HEALTH CARE WORKERS

    Directory of Open Access Journals (Sweden)

    Gh. Pouryaghoub

    2008-04-01

    Full Text Available Latex allergy has become an occupational hazard among healthcare workers. Atopy, intensity and duration of exposure have been recognized as predisposing factors for latex sensitization. Frequency of sensitization varies among countries. So we decided to investigate the prevalence of latex sensitization and potential risk factors among healthcare workers in a general hospital. In a cross sectional study by distributing a questionnaire among 876 employees of a general hospital, we investigated the prevalence of latex allergy and the potential risk factors for latex sensitization. We collected information about occupational history, including specific tasks performed, time of first exposure to latex, number of pairs of gloves used, and duration of weekly exposure. We also investigated the interval between first exposure and onset of symptoms. We asked about pre-existing rhinoconjuctivitis, asthma, atopic and contact dermatitis, hay fever, autoimmune diseases, and food allergies. This survey documented a high prevalence of adverse reaction to all latex containing materials (52.5%. 37.7% of responder had adverse reaction to latex gloves. The highest prevalence of adverse reaction to all latex containing materials was found in the surgical operating room, followed by emergency unit and internal medicine wards. According to this study, frequency of adverse reaction to latex was high among health care workers. This may be due to relatively low response rate, low quality of latex products in Iran, and the method of measurement. Whenever, the need for implementing prevention program, using latex-free methods and training of employees to reduce adverse reaction to latex is apparent.

  14. Latex allergy: a health care problem of epidemic proportions.

    Science.gov (United States)

    Agarwal, Sanjay; Gawkrodger, David J

    2002-01-01

    Latex allergy is one of the major health concerns of the decade. The induction of latex allergy commonly occurs after exposure of skin or mucous membrane to natural rubber latex. It is usually a type I, immediate hypersensitivity reaction mediated by IgE which can range from mild skin erythema to anaphylaxis and death. To manage latex allergy appropriately, prompt and correct diagnosis is essential. This depends primarily on clinical history, latex specific IgE RAST (in vitro) and skin prick test (in vivo). It affects people who are frequently exposed to products made of natural rubber latex, such as, health care workers, workers in the rubber industry and those who have had multiple surgical operations. The prevalence in the general population was estimated at 0.7% in a population study in France, but this can be higher in health care workers (up to 17%) and in patients with spina bifida to almost 65%. Prevention strategies should therefore target at risk population, rather than the population as a whole. At present this primarily involves providing non-powdered latex gloves in hospitals and primary health care centres. However, once latex allergy has been established, the situation becomes more complicated. Health care workers either have to be moved to a latex free environment or in extreme circumstances may have to give up their occupation. For patients undergoing operations most hospitals have adopted a latex free protocol. It is important that this is understood and followed by every member of the staff. Those who have had serious adverse reactions should wear Medi-Alert bracelets and in exceptional circumstances may need to keep epinephrine injections on their person. Future strategies focus on the reduction of allergens during latex manufacture, development of suitable non latex gloves and immunotherapy including desensitisation of latex allergic individuals and development of candidate vaccine.

  15. Comparative study between novel self cross-linking and conventional fluorinated acrylic latex

    Institute of Scientific and Technical Information of China (English)

    Li Jun Chen

    2011-01-01

    Novel self cross-linking fluorinated acrylic latex (SCLFAL) has been successfully prepared via starved seeded semi-batch emulsion polymerization. The resultant SCLFAL is characterized by Fourier transform infrared (FTTR) spectrometry. Contact angle (CA) and glass transition temperature (Tg) of the film are investigated. Results show that CA and Tg of the film can be improved when the moderate amount of HPMA is introduced into the mixed monomers.

  16. HPMA and HEMA copolymer bead interactions with eukaryotic cells

    Directory of Open Access Journals (Sweden)

    Cristina D. Vianna-Soares

    2004-09-01

    Full Text Available Two different hydrophilic acrylate beads were prepared via aqueous suspension polymerization. Beads produced of a hydroxypropyl methacrylate (HPMA and ethyleneglycol methacrylate (EDMA copolymer were obtained using a polyvinyl alcohol suspending medium. Copolymers of 2hydroxyethyl methacrylate (HEMA, methyl methacrylate (MMA and ethyleneglycol methacrylate (EDMA beads were obtained using magnesium hydroxide as the suspending agent. Following characterization by scanning electron microscopy (SEM, nitrogen sorption analysis (NSA and mercury intrusion porosimetry (MIP, the beads were cultured with monkey fibroblasts (COS7 to evaluate their ability to support cell growth, attachment and adhesion. Cell growth behavior onto small HPMA/EDMA copolymer beads and large HEMA/MMA/EDMA copolymer beads is evaluated regarding their hidrophilicity/hidrophobicity and surface roughness.

  17. Synthesis of Polyacrylate/Polysiloxane Copolymer and Its Damping Performance

    Institute of Scientific and Technical Information of China (English)

    夏宇正; 石淑先; 焦书科; 李素青

    2003-01-01

    The copolymer of polyacrylate/polysiloxane for vibration damping materials was synthesized through emulsion polymerization. The effects of the amount of methyl methacrylate (MMA),polysiloxane containing vinyl, initiator and emulsifier on the conversion, stability of polyacrylate/polysiloxane emulsion were discussed when the emulsion was prepared by pre-emulsifying half continuous method. The graft copolymer has good vibration damping performance. The widest glass transition region of the copolymer spans 100℃, and the highest value of tanδ reached 2.0. The glass transition of the samples was examined by dynamic mechanical analysis (DMA). The vibration damping performance of the graft copolymer was affected by the amount of poly-vinyl dimethylsiloxane (PVMS).

  18. BARRIER PROPERTY AND STRUCTURE OF ACRYLONITRILE/ACRYLIC COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    YANG Zhenghua; LI Yuesheng

    1997-01-01

    A series of acrylonitrile (AN) copolymers with methyl acrylate (MA) or ethyl acrylate (EA) as comonomer (5-23 wt%) was prepared by free-radical copolymerization. The permeability coefficients of the copolymers to oxygen and carbon dioxide were measured at 1.0 MPa and at 30 ℃, and those to water vapor also measured at 100% relative humidity and at 30 ℃. All the AN/acrylic copolymers are semicrystalline. As the acrylate content increase, the permeability coefficients of the copolymers to oxygen and carbon dioxide are increased progressively, but those to water vapor are decreased progressively. The gas permeability coefficients of the polymers were correlated with free-volume fractions or the ratio of free volume to cohesive energy.

  19. Sulfonated macro-RAFT agents for the surfactant-free synthesis of cerium oxide-based hybrid latexes.

    Science.gov (United States)

    Garnier, Jérôme; Warnant, Jérôme; Lacroix-Desmazes, Patrick; Dufils, Pierre-Emmanuel; Vinas, Jérôme; van Herk, Alex

    2013-10-01

    Three types of amphiphatic macro-RAFT agents were employed as compatibilizers to promote the polymerization reaction at the surface of nanoceria for the synthesis of CeO2-based hybrid latexes. Macro-RAFT copolymers and terpolymers were first synthesized employing various combinations of butyl acrylate as a hydrophobic monomer and acrylic acid (AA) and/or 2-acrylamido-2-methylpropane sulfonic acid (AMPS) as hydrophilic monomers. After characterizing the adsorption of these macro-RAFT agents at the cerium oxide surface by UV-visible spectrometry, emulsion copolymerization reactions of styrene and methyl acrylate were then carried out in the presence of the surface-modified nanoceria. Dynamic Light Scattering and cryo-Transmission Electron Microscopy were employed to confirm the hybrid structure of the final CeO2/polymer latexes, and proved that the presence of acrylic acid units in amphiphatic macro-RAFT agents enabled an efficient formation of hybrid structures, while the presence of AMPS units, when combined with AA units, resulted in a better distribution of cerium oxide nanoclusters between latex particles.

  20. Proteolytic properties of Funastrum clausum latex.

    Science.gov (United States)

    Morcelle, Susana R; Caffini, Néstor O; Priolo, Nora

    2004-07-01

    As part of a screening of latex endopeptidases from plants growing in Argentina, the presence of proteolytic activity in the latex of Funastrum clausum stems is reported. The proteases present in the crude extract showed the main characteristics of the cysteine proteolytic class, i.e. optimum pH at alkaline range, isoelectric point (pI) higher than 9.0, and inhibition of proteolytic activity by thiol blocking reagents. A remarkable thermal stability was also evident in the crude extract. Endosterolytic preference tried on p-nitrophenyl esters of N-alpha-carbobenzoxy-L-amino acids was higher for the alanine, asparagine and tyrosine derivatives. Preliminary peptidase purification by two-step ionic exchange showed the presence of two proteolytic fractions with molecular masses of approximately 24.0 kDa according to SDS-PAGE.

  1. Latex migration in battery slurries during drying.

    Science.gov (United States)

    Lim, Sanghyuk; Ahn, Kyung Hyun; Yamamura, Masato

    2013-07-02

    We used real-time fluorescence microscopy to investigate the migration of latex particles in drying battery slurries. The time evolution of the fluorescence signals revealed that the migration of the latex particles was suppressed above the entanglement concentration of carboxymethyl cellulose (CMC), while it was significantly enhanced when CMC fully covered the surfaces of the graphite particles. In particular, a two-step migration was observed when the graphite particles flocculated by depletion attraction at high CMC/graphite mass ratios. The transient states of the nonadsorbing CMC and graphite particles in a medium were discussed, and the uses of this novel measurement technique to monitor the complex drying processes of films were demonstrated.

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

    Science.gov (United States)

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

    2014-06-01

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

  3. Mechanisms of fibrinogen adsorption on latex particles determined by zeta potential and AFM measurements.

    Science.gov (United States)

    Adamczyk, Zbigniew; Bratek-Skicki, Anna; Dąbrowska, Paulina; Nattich-Rak, Małgorzata

    2012-01-10

    The adsorption of fibrinogen on polystyrene latex particles was studied using the concentration depletion method combined with the AFM detection of residual protein after adsorption. Measurements were carried out for a pH range of 3.5-11 and an ionic strength range of 10(-3)-0.15 M NaCl. First, the bulk physicochemical properties of fibrinogen and the latex particle suspension were characterized for this range of pH and ionic strength. The zeta potential and the number of uncompensated (electrokinetic) charges on the protein were determined from microelectrophoretic measurements. It was revealed that fibrinogen molecules exhibited amphoteric characteristics, being on average positively charged for pH adsorption of fibrinogen on latex for pH below 11. It was also proven that fibrinogen adsorption was irreversible, with the maximum surface concentration varying between 2.5 and 5 × 10(3) μm(-2) (weight concentration of a bare molecule was 1.4 to 2.8 mg m(-2)). These measurements revealed two main adsorption mechanisms of fibrinogen: (i) the unoriented (random) mechanism prevailing for lower ionic strength, where adsorbing molecules significantly penetrate the fuzzy polymeric layer on the latex core and (ii) the side-on adsorption mechanism prevailing for pH > 5.8 and a higher ionic strength of 0.15 M. It was also shown that in the latter case, variations in the zeta potential with the protein coverage could be adequately described in terms of the electrokinetic model, previously formulated for planar substrate adsorption. On the basis of these experimental data, an efficient procedure of preparing fibrinogen-covered latex particles of controlled monolayer structure and coverage was envisaged.

  4. [Detection of pentachlorophenol in natural rubber latex].

    Science.gov (United States)

    Jaworska, E

    1976-01-01

    The method of detection of pentachlorophenol in natural rubber latex is proposed. Pentachlorophenol is isolated from other nonrubber-like substances by thin-layer chromatography and identified by spectroscopic method in UV-light. Isolation of pentachlorophenol is carried out from water extracts obtained from the dry caoutchouc films, so the same method can be used for examination of the rubber articles designed for the medicinetoo.

  5. New Polytetrahydrofuran Graft Copolymers.

    Science.gov (United States)

    1979-03-15

    chioroprene) , chiorobutyl - ~~~~~ rubber , bromobutyl rubber , chlorinated EPDM , chlorinated poly(buta— diene) and chlorinated butadiene styrene copolymer...for initial detailed studies (3 ,4 , 6 , 7 — 9 ) . Many soluble metal salts with cations capable of stabilizing an on].um ion polymerization (SO3CF 3

  6. Block coordination copolymers

    Science.gov (United States)

    Koh, Kyoung Moo; Wong-Foy, Antek G; Matzger, Adam J; Benin, Annabelle I; Willis, Richard R

    2012-11-13

    The present invention provides compositions of crystalline coordination copolymers wherein multiple organic molecules are assembled to produce porous framework materials with layered or core-shell structures. These materials are synthesized by sequential growth techniques such as the seed growth technique. In addition, the invention provides a simple procedure for controlling functionality.

  7. Investigation of some copolymers based on acrylic salts as circulation loss control agents

    Directory of Open Access Journals (Sweden)

    Ahmed Mohamed Alsabagh

    2013-12-01

    The prepared copolymers were investigated as loss circulation control materials by measuring different filtration parameters such as; spurt loss, fluid loss and permeability plugging tester value according to the American Petroleum Institute (API standard. From the obtained data, it was found that the 0.6% from the poly[PA-co-AM](0.4:0.6 exhibited the best results of the filtration parameters among the other copolymers. At the same time all the studied copolymers enhanced the rheological properties of the drilling mud. These results were discussed on the light of the swelling capacity of the copolymers.

  8. Self-assembly of block copolymers on topographically patterned polymeric substrates

    Energy Technology Data Exchange (ETDEWEB)

    Russell, Thomas P.; Park, Soojin; Lee, Dong Hyun; Xu, Ting

    2016-05-10

    Highly-ordered block copolymer films are prepared by a method that includes forming a polymeric replica of a topographically patterned crystalline surface, forming a block copolymer film on the topographically patterned surface of the polymeric replica, and annealing the block copolymer film. The resulting structures can be used in a variety of different applications, including the fabrication of high density data storage media. The ability to use flexible polymers to form the polymeric replica facilitates industrial-scale processes utilizing the highly-ordered block copolymer films.

  9. A method for protein extraction from different subcellular fractions of laticifer latex in Hevea brasiliensis compatible with 2-DE and MS

    Directory of Open Access Journals (Sweden)

    Guo Anping

    2010-06-01

    Full Text Available Abstract Background Proteomic analysis of laticifer latex in Hevea brasiliensis has been received more significant attentions. However, the sticky and viscous characteristic of rubber latex as cytoplasm of laticifer cells and the complication of laticifer latex membrane systems has made it challenge to isolate high-quality proteins for 2-DE and MS. Results Based on the reported Borax/PVPP/Phenol (BPP protocol, we developed an efficient method for protein preparation from different latex subcellular fractions and constructed high-resolution reference 2-DE maps. The obtained proteins from both total latex and C-serum fraction with this protocol generate more than one thousand protein spots and several hundreds of protein spots from rubber particles as well as lutoid fraction and its membranes on the CBB stained 2-DE gels. The identification of 13 representative proteins on 2-DE gels by MALDI TOF/TOF MS/MS suggested that this method is compatible with MS. Conclusion The proteins extracted by this method are compatible with 2-DE and MS. This protein preparation protocol is expected to be used in future comparative proteomic analysis for natural rubber latex.

  10. Novel fluorinated block copolymer architectures fuelled by atom transfer radical polymerization

    DEFF Research Database (Denmark)

    Jankova, Katja; Hvilsted, Søren

    2005-01-01

    Block copolymers based on poly(pentafluorostyrene), PFS, in various numbers and of different lengths, and polystyrene are prepared by atom transfer radical polymerization (ATRP). Di- and triblock copolymers with varying amounts of PFS were synthesized employing either I phenylethylbromide or 1,4-...

  11. Development of a rubber elongation factor, surface-imprinted polymer-quartz crystal microbalance sensor, for quantitative determination of Hev b1 rubber latex allergens present in natural rubber latex products.

    Science.gov (United States)

    Sontimuang, Chonlatid; Suedee, Roongnapa; Canyuk, Bhutorn; Phadoongsombut, Narubodee; Dickert, Franz L

    2011-02-21

    Molecularly imprinted polymers (MIPs) for screening to detect rubber latex allergens (Hev b1) in natural rubber based products were designed as artificial recognition polymeric materials coated onto a quartz crystal microbalance (QCM). The polymers were prepared using a stamp imprinting procedure after mixing optimum amounts of methacrylic acid-vinylpyrrolidone-dihydroxyethylene bisacrylamide and Hev b1 latex allergen proteins, obtained from rubber gloves. QCM measurements showed that the resulting polymer layers after removal of the proteins used in their preparation could incorporate structures and features down to nanometer scale of protein templates into the imprinted polymer much better than a non-specific control polymer under controlled sensor conditions and an optimized polymerization process. This selective polymer but not the non-selective polymer clearly distinguished between the latex allergen Hev b1 and proteins such as lysozyme, ovalbumin and bovine serum albumin, with a selectivity factor of from 2 to 4, and the response of the rubber elongation factors by an astonishing factor of 12. The imprinted cavities recognized specific binding sites and could distinguish among related hevein latex allergenic proteins isolated from fresh natural rubber latex; Hev b1, Hev b2, and Hev b3 with a selectivity factor of from 4 to 6. The different QCM measurements obtained presumably reflected slightly different conformations and affinities to the MIP binding sites. The sensor layers selectively adsorbed Hev b1 within minutes in amounts ranging from 10 to 1500 μg L⁻¹ and with a detection limit of 1 μg L⁻¹. This work has demonstrated that this new sensor provides a fast and reliable response to natural rubber latex protein, even after being extracted from the matrix of rubber gloves.

  12. Mosquito larvicidal and silver nanoparticles synthesis potential of plant latex

    OpenAIRE

    H.P. Borase; C.D. Patil; R.B. Salunkhe; C.P. Narkhede; R.K. Suryawanshi; Salunke, B. K.; PATIL S. V

    2014-01-01

    Silver nanoparticles (AgNPs) were synthesized from the latex of the medicinally important plants Euphorbia milii, Euphorbia hirta, Ficus racemosa and Jatropha curcas. Synthesized AgNPs were characterized by UV-Vis spectrophotometry, scanning electron microscopy, energy dispersive X-ray analysis, X-ray diffraction, Fourier transformed infrared spectroscopy, particle size, and zeta potential analysis. Potency of latex and latex-synthesized AgNPs was evaluated against the 2nd and 4th instar larv...

  13. Polymer Electrolyte Membrane Fuel Cell Performance of a Sulfonated Poly(Arylene Ether Benzimidazole Copolymer Membrane

    Directory of Open Access Journals (Sweden)

    Hasan Ferdi Gerçel

    2016-01-01

    Full Text Available Disodium-3,3′-disulfonate-4,4′-dichlorodiphenylsulfone (SDCDPS and 5,5′-bis[2-(4-hydroxyphenylbenzimidazole] (HPBI monomers were synthesized. Binding these monomers via nucleophilic aromatic polycondensation reaction, a sulfonated poly(arylene ether benzimidazole copolymer was synthesized. Structures of monomers and copolymer were confirmed by proton nuclear magnetic resonance spectroscopy (1H NMR and Fourier transform infrared (FTIR spectroscopy analyses. Proton exchange membrane was prepared by dissolving copolymer in dimethylacetamide (DMAc and casting onto a glass plate. Copolymer membrane was doped with sulfuric acid to ensure proton exchange character. Single cell performance of the copolymer membrane was tested in a polymer electrolyte membrane fuel cell test station. The highest power density of the membrane was measured as 23.7 mW cm−2 at 80°C. Thermogravimetric analysis (TGA showed that as the degree of disulfonation is increased thermal stability of the copolymer is increased.

  14. Synthesis and Characterization of a Systematic Series of All-Conjugated Diblock Copolymers

    Science.gov (United States)

    Smith, Kendall; Verduzco, Rafael

    2012-02-01

    All-conjugated block copolymers can potentially self-assemble into nanoscale structures beneficial for charge separation and transport, but due to synthetic challenges a comprehensive investigation of all-conjugated block copolymers has not been carried out . Here we detail a novel synthetic approach to all-conjugated block copolymers and characterize the structure of a systematic series of materials. The materials are prepared via copper-catalyzed azide-alkyne click chemistry followed by selective solvent removal of homopolymer impurities. This allows us to readily vary the molecular weight and type of each block in order to systematically study the properties of a family of block copolymers. As a system relevant to organic photovoltatics, we investigate a series of diblock copolymers based on poly(9,9-dioctyl-fluorene) and poly(3-alkylthiophene). This series of block copolymers is characterized with respect to phase behavior, including micro-phase segregation and crystallinity, optical properties, and charge mobilities.

  15. Synthesis and Characterization of Poly(L-lactide-co-ε-caprolactone) Copolymers

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    A series of random and block poly (L-lactide-co-ε-caprolactone) (PCLA) copolymers with different composition are prepared using starmous octaoate as catalyst. The effects of the amount of initiator on the intrinsic viscosity have been investigated. The structure of the PCLA copolymers is characterized by means of nuclear magnetic resonance (NMR), Fourier transform infrared spectrum (FTIR), differential scanning calorimetry(DSC) and X- ray diffraction (XRD) methods. It is shown that the synthesis condition and the composition of copolymers have obvious influence on the structure of PCLA copolymers. Hydrolytic degradation of the copolymers in a PBS solution of pH 7.4 at 37.0 ℃ shows that the copolymers of different compositions degrade at different rates .

  16. Self-assembly of latex particles for colloidal crystals

    Institute of Scientific and Technical Information of China (English)

    Zhirong Li; Jingxia wang; Yanlin Song

    2011-01-01

    Self-assembly of latex particles is of great importance for fabricating various functional colloidal crystals.In this paper,we review recent research on the self-assembly of latex particles for colloidal crystals,covering the assembly forces and various assembly approaches of latex particles,including self-assembly by gravity sedimentation,vertical deposition,physical confinement,electric field,and magnetic field.Furthermore,some simple methods for assembling latex particles such as spin coating,spray coating,and printing are also summarized.

  17. New constitutive latex osmotin-like proteins lacking antifungal activity.

    Science.gov (United States)

    Freitas, Cleverson D T; Silva, Maria Z R; Bruno-Moreno, Frederico; Monteiro-Moreira, Ana C O; Moreira, Renato A; Ramos, Márcio V

    2015-11-01

    Proteins that share similar primary sequences to the protein originally described in salt-stressed tobacco cells have been named osmotins. So far, only two osmotin-like proteins were purified and characterized of latex fluids. Osmotin from Carica papaya latex is an inducible protein lacking antifungal activity, whereas the Calotropis procera latex osmotin is a constitutive antifungal protein. To get additional insights into this subject, we investigated osmotins in latex fluids of five species. Two potential osmotin-like proteins in Cryptostegia grandiflora and Plumeria rubra latex were detected by immunological cross-reactivity with polyclonal antibodies produced against the C. procera latex osmotin (CpOsm) by ELISA, Dot Blot and Western Blot assays. Osmotin-like proteins were not detected in the latex of Thevetia peruviana, Himatanthus drasticus and healthy Carica papaya fruits. Later, the two new osmotin-like proteins were purified through immunoaffinity chromatography with anti-CpOsm immobilized antibodies. Worth noting the chromatographic efficiency allowed for the purification of the osmotin-like protein belonging to H. drasticus latex, which was not detectable by immunoassays. The identification of the purified proteins was confirmed after MS/MS analyses of their tryptic digests. It is concluded that the constitutive osmotin-like proteins reported here share structural similarities to CpOsm. However, unlike CpOsm, they did not exhibit antifungal activity against Fusarium solani and Colletotrichum gloeosporioides. These results suggest that osmotins of different latex sources may be involved in distinct physiological or defensive events.

  18. Study on radiation vulcanization of natural rubber latex

    Institute of Scientific and Technical Information of China (English)

    ZhuNan-Kang; MakuuchiK; 等

    1997-01-01

    The effect of dose rate of 60Co γ-ray on radiation vulacnization of natural rubber latex is studied using Malysian latex with 0.002 mass fraction KOH and 0.05 mass fraction n-BA.Results show that,when radiation doses are 20 and 15kGy,only that the dose rates are greater than 0.49 and 1.6 kGY/h,respectively can make the tensile strength of latex film meet the related standard;besides,storage time of radiation vulcanization latex has no effect on physical properties of the film.

  19. Anthelmintic activity of latex of Jatropha curcas (ratanjot

    Directory of Open Access Journals (Sweden)

    Mr. Hitesh Kumar Parmar

    2014-03-01

    Full Text Available A multitude of plants have been used for the treatment of helmenthiasis throughout the world. One such plant is Jatropha curcas. It is known as ratanjot or biodiesel plant, which belongs to the family Euphorbiaceae. It possesses many uses like antidiabetic, antmicrobial and antioxidant. The phytochemical prospection of the fresh and dried latex showed the presence of different classes of secondary metabolites that have demonstrated antimicrobial action. The present research work investigated the Anthelmintic activity of latex of leaves of Jatropha curcas. The major finding of the present work illustrates that aqueous latex of Jatropha curcas has shown better Anthelmintic activity than control Jatropha latex and standard drug, piperazine citrate.

  20. Novel block, graft and random copolymers for biomedical applications

    DEFF Research Database (Denmark)

    Javakhishvili, Irakli; Jankova Atanasova, Katja; Tanaka, Masaru;

    roles for this [2]. An artificial lung (oxygenator), already in use, is coated with high MW PMEA prepared by radical polymerization with AIBN [2]. To broaden the possibilities for designing biomedical devices [3] and inspired from these findings we first prepared homo polymers of MEA and their block...... copolymers with MMA [4] utilizing ATRP. Here we present other block, graft and random copolymers of MEA intended for biomedical applications. These macromolecular architectures have been constructed by employing controlled radical polymerization methods such as RAFT and ATRP....

  1. Structural and Luminescence Properties of Lu2O3:Eu3+ F127 Tri-Block Copolymer Modified Thin Films Prepared by Sol-Gel Method

    Directory of Open Access Journals (Sweden)

    María Luz Carrera Jota

    2013-02-01

    Full Text Available Lu2O3:Eu3+ transparent, high density, and optical quality thin films were prepared using the sol-gel dip-coating technique, starting with lutetium and europium nitrates as precursors and followed by hydrolysis in an ethanol-ethylene glycol solution. Acetic acid and acetylacetonate were incorporated in order to adjust pH and as a sol stabilizer. In order to increment the thickness of the films and orient the structure, F127 Pluronic acid was incorporated during the sol formation. Structural, morphological, and optical properties of the films were investigated for different F127/Lu molar ratios (0–5 in order to obtain high optical quality films with enhanced thickness compared with the traditional method. X-ray diffraction (XRD shows that the films present a highly oriented cubic structure beyond 1073 K for a 3-layer film, on silica glass substrates. The thickness, density, porosity, and refractive index evolution of the films were investigated by means of m-lines microscopy along with the morphology by scanning electron microscope (SEM and luminescent properties.

  2. Follow-up Study of Latex-allergic Health Care Workers in Japan

    Directory of Open Access Journals (Sweden)

    Akiko Yagami

    2006-01-01

    Conclusions: After avoiding latex products and following our educational suggestions, the patients' allergy symptoms had generally improved. This indicates that our countermeasures against latex allergy were largely successful.

  3. Preparation and application of the sol-gel-derived acrylate/silicone co-polymer coatings for headspace solid-phase microextraction of 2-chloroethyl ethyl sulfide in soil.

    Science.gov (United States)

    Liu, Mingming; Zeng, Zhaorui; Fang, Huaifang

    2005-05-27

    Three types of novel acrylate/silicone co-polymer coatings, including co-poly(methyl acrylate/hydroxy-terminated silicone oil) (MA/OH-TSO), co-poly(methyl methacrylate/OH-TSO) (MMA/OH-TSO) and co-poly(butyl methacrylate/OH-TSO) (BMA/OH-TSO), were prepared for the first time by sol-gel method and cross-linking technology and subsequently applied to headspace solid-phase microextraction (HS-SPME) of 2-chloroethyl ethyl sulfide (CEES), a surrogate of mustard, in soil. The underlying mechanisms of the coating process were discussed and confirmed by IR spectra. The selectivity of the three types of sol-gel-derived acrylate/silicone coated fibers was studied, and the BMA/OH-TSO coated fibers exhibited the highest extraction ability to CEES. The concentration of BMA and OH-TSO in sol solution was optimized, and the BMA/OH-TSO (3:1)-coated fibers possessed the highest extraction efficiency. Compared with commercially available polyacrylate (PA) fiber, the sol-gel-derived BMA/OH-TSO (3:1) fibers showed much higher extraction efficiency to CEES. Therefore, the BMA/OH-TSO (3:1)-coated fibers were chosen for the analysis of CEES in soil matrix. The reproducibility of coating preparation was satisfactory, with the RSD 2.39% within batch and 3.52% between batches, respectively. The coatings proved to be quite stable at high temperature (to 350 degrees C) and in different solvents (organic or inorganic), thus their lifetimes (to 150 times) are longer than conventional fibers. Extraction parameters, such as the volume of water added to the soil, extraction temperature and time, and the ionic strength were optimized. The linearity was from 0.1 to 10 microg/g, the limit of detection (LOD) was 2.7 ng/g, and the RSD was 2.19%. The recovery of CEES was 88.06% in agriculture soil, 92.61% in red clay, and 101.95% in sandy soil, respectively.

  4. Latex agglutination assays for detection of non-O157 Shiga toxin-producing Escherichia coli serogroups O26, O45, O103, O111, O121, and O145.

    Science.gov (United States)

    Medina, Marjorie B; Shelver, Weilin L; Fratamico, Pina M; Fortis, Laurie; Tillman, Glenn; Narang, Neelam; Cray, William C; Esteban, Emilio; Debroy, Andchitrita

    2012-05-01

    Latex agglutination assays utilizing polyclonal antibodies were developed for the top six non-O157 Shiga toxin-producing Escherichia coli (STEC) serogroups. Rabbit antisera were affinity purified through protein A/G columns, and the isolated immunoglobulins (IgGs) were covalently immobilized onto polystyrene latex particles. The resulting latex-IgG complex had a protein (IgG) load of 0.20 to 0.28 mg/ml in a 1% latex suspension. Optimum conditions for the agglutination assay consisted of utilizing 20 μm l of latex-IgG reagent containing 2.0 to 2.8 μm g IgG in a 0.5% latex suspension. Agglutination or flocculation was observed almost instantly after mixing the colonies with the latex-IgG, indicating STEC strains. More than 100 target and nontarget strains were tested in more than 3,000 test replicates. All target organisms produced positive results, but three antisera (anti-O26, anti-O103, and anti-O145) cross-reacted with some other STECs. The anti-O103 and anti-O145 latex reagents cross-reacted with O26 strains, and the anti-O26 cross-reacted with O103 strains. The latex-IgG reagents are stable for at least 1 year and are easy to prepare. These agglutination assays can be used for identification of presumptive non-O157 STEC colonies from agar media. The techniques used to prepare the latex reagents also can be utilized for testing other STEC serogroups, other E. coli serotypes, or other pathogens to ensure safe foods to consumers.

  5. Ocular permeability of pirenzepine hydrochloride enhanced by methoxy poly(ethylene glycol)-poly(D, L-lactide) block copolymer.

    Science.gov (United States)

    Tu, Jiasheng; Pang, Hui; Yan, Zhen; Li, Pengmei

    2007-10-01

    Methoxy poly(ethylene glycol)-poly(D, L-lactide) block copolymer was tested as an ocular permeation enhancer for pirenzepine hydrochloride. The block copolymers with the methoxy poly(ethylene glycol) to poly(D, L-lactide) weight ratio of 80/20, 50/50, 40/60 were synthesized by a ring-opening polymerization procedure. In vitro transcorneal experiments demonstrated that the block copolymer 80/20 significantly enhanced the transcorneal permeation of pirenzepine at the mass ratio of 1/1.4 (pirenzepine hydrochloride/copolymer). Interaction between pirenzepine and copolymer was identified by infrared spectroscopy analysis and dialysis experiments. Ocular pharmacokinetics of pirenzepine/copolymer preparation by in vivo instillation experiments confirmed that block copolymer could enhance the ocular penetration of pirenzepine. Ocular chronic toxicity experiments of block copolymer and pirenzepine/copolymer preparation were studied on rabbits, and no significant toxicity in both groups was observed within 9 months. It could conclude that pirenzepine/copolymer preparation is effective and safe in ocular delivery of pirenzepine.

  6. The effect of acrylic latex-based polymer on cow blood adhesive resins for wood composites

    Science.gov (United States)

    Yan, J.; Lin, H. L.; Feng, G. Z.; Gunasekaran, S.

    2016-07-01

    In this paper, alkali-modified cow blood adhesive (BA) and blood adhesive/acrylic latex-based adhesive (BA/ALB) were prepared. The physicochemical and adhesion properties of cow blood adhesive such as UV- visible spectra, particle size, viscosity were evaluated; share strength, water resistance were tested. UV- visible spectra indicates that the strong bonding strength of BA/ALB appeared after incorporating; the particle size of adhesive decreased with the increase of ALB concentration, by mixing ALB and BA, hydrophilic polymer tends locate or extand the protein chains and provide stability of the particles; viscosity decreased as shear rate increased in concordance with a pseudoplastic behavior; both at dry and soak conditions, BA and ALB/BA show significant difference changes when mass fraction of ALB in blend adhesive was over 30% (p latex-based adhesive significantly increased the strength and water resistance of the resulting wood.

  7. texreg: Conversion of Statistical Model Output in R to LATEX and HTML Tables

    Directory of Open Access Journals (Sweden)

    Philip Leifeld

    2013-11-01

    Full Text Available A recurrent task in applied statistics is the (mostly manual preparation of model output for inclusion in LATEX, Microsoft Word, or HTML documents usually with more than one model presented in a single table along with several goodness-of-fit statistics. However, statistical models in R have diverse object structures and summary methods, which makes this process cumbersome. This article first develops a set of guidelines for converting statistical model output to LATEX and HTML tables, then assesses to what extent existing packages meet these requirements, and finally presents the texreg package as a solution that meets all of the criteria set out in the beginning. After providing various usage examples, a blueprint for writing custom model extensions is proposed.

  8. STUDY ON PET-PA66 COPOLYMER

    Institute of Scientific and Technical Information of China (English)

    WU Rongrui; SHI Weitong

    1992-01-01

    In this work the PET-PA66 copolymers are obtained. The characterization of chemical structure of copolymer chain by NMR method is also given . It is shown that when the 66 Nylon salt is added in the copolycondensation, the adipic acid and hexamethylenediamine reacted mainly by itself and the obtained copolymer is a random copolymer, and when the Nylon 66 oligomer is added, the obtained copolymer is a block copolymer. The result of NMR analysis is demonstrated by properties investigation.

  9. Block copolymer battery separator

    Energy Technology Data Exchange (ETDEWEB)

    Wong, David; Balsara, Nitash Pervez

    2016-04-26

    The invention herein described is the use of a block copolymer/homopolymer blend for creating nanoporous materials for transport applications. Specifically, this is demonstrated by using the block copolymer poly(styrene-block-ethylene-block-styrene) (SES) and blending it with homopolymer polystyrene (PS). After blending the polymers, a film is cast, and the film is submerged in tetrahydrofuran, which removes the PS. This creates a nanoporous polymer film, whereby the holes are lined with PS. Control of morphology of the system is achieved by manipulating the amount of PS added and the relative size of the PS added. The porous nature of these films was demonstrated by measuring the ionic conductivity in a traditional battery electrolyte, 1M LiPF.sub.6 in EC/DEC (1:1 v/v) using AC impedance spectroscopy and comparing these results to commercially available battery separators.

  10. Block copolymer battery separator

    Science.gov (United States)

    Wong, David; Balsara, Nitash Pervez

    2016-04-26

    The invention herein described is the use of a block copolymer/homopolymer blend for creating nanoporous materials for transport applications. Specifically, this is demonstrated by using the block copolymer poly(styrene-block-ethylene-block-styrene) (SES) and blending it with homopolymer polystyrene (PS). After blending the polymers, a film is cast, and the film is submerged in tetrahydrofuran, which removes the PS. This creates a nanoporous polymer film, whereby the holes are lined with PS. Control of morphology of the system is achieved by manipulating the amount of PS added and the relative size of the PS added. The porous nature of these films was demonstrated by measuring the ionic conductivity in a traditional battery electrolyte, 1M LiPF.sub.6 in EC/DEC (1:1 v/v) using AC impedance spectroscopy and comparing these results to commercially available battery separators.

  11. A Photosensitive Copolymer for UV-curable Eleetrodeposition Coatings

    Institute of Scientific and Technical Information of China (English)

    LIU Ren; LI Xiaojie; AN Fenglci; ZHANG Shengwen; LIU Xiaoya

    2011-01-01

    A series of photosensitive random copolymers (UPDHES) were prepared by introducing acrylate groups onto the side chain of the copolymer backbone of N,N-domethyl amimethyl methacrylate (DMAEMA),2-hydroxypropyl acrylate (HEA),2-ethylhexyl acrylate (EHA),and styrene (St) (PDHES).The molecular structure of UPDHES was characterized by FTIR,1HNMR and GPC.The photopolymerization kinetics of UPDHES with different C=C content was investigated using real time FTIR in which it was found that the UPDHES system had notable photosensitivity.The effect of C=C content on the properties of cured films were studied by evaluating various film properties such as thermal stability,glass transition temperature and tensile properties.The thermal degradation of cured films was investigated via thermogravimetric analysis/infrared spectrometry (TGA-IR).Thus a series of UV-curable electrodeposition coatings with good photosensitivity and mechanical properties were prepared from a low-cost photosensitive random copolymer.

  12. Preparation

    Directory of Open Access Journals (Sweden)

    M.M. Dardir

    2014-03-01

    Full Text Available Some hexanamide-mono and di-linoleniate esters were prepared by the reaction of linolenic acid and hexanamide (derived from the reaction of hexanoic acid and diethanolamine. The chemical structure for the newly prepared hexanamide-mono and di-linoleniate esters were elucidated using elemental analysis, (FTIR, H 1NMR and chemical ionization mass spectra (CI/Ms spectroscopic techniques. The results of the spectroscopic analysis indicated that they were prepared through the right method and they have high purity. The new prepared esters have high biodegradability and lower toxicity (environmentally friendly so they were evaluated as a synthetic-based mud (ester-based mud for oil-well drilling fluids. The evaluation included study of the rheological properties, filtration and thermal properties of the ester based-muds formulated with the newly prepared esters compared to the reference commercial synthetic-based mud.

  13. Antimicrobial activity of latex silver nanoparticles using Calotropis procera

    Directory of Open Access Journals (Sweden)

    Nadia Hussein Mohamed

    2014-11-01

    Conclusions: It can be concluded that serum latex of Calotropis procera was found to display strong potential for the synthesis of AgNPs as antimicrobial agents through rapid reduction of silver ions (Ag+ to Ag0. The green synthesized AgNPs were found to show higher antimicrobial efficacy than crude latex.

  14. A comparison of different LaTeX programs

    NARCIS (Netherlands)

    Koning, Ruud H.

    2001-01-01

    In this review two commercial and two freeware LaTeX implementations are discussed and compared: teTeX (Linux, Unix) pcTeX32 (Windows 3.1, Windows95/98/NT) Scientific Workplace (Windows95/98/NT) mikTeX (Windows95/98/NT) Keywords: LaTeX, word processing

  15. Installing fonts in LaTeX a user's experience

    NARCIS (Netherlands)

    Hanssen, Ferdy

    2003-01-01

    This paper presents a user's experience with installing fonts for use in LaTeX. It will be shown that it is not hard to make a standard Type 1 font work, if you use modern font installation software for LaTeX. All the steps necessary to install the example fonts will be shown. The example fonts used

  16. Installing fonts in LaTeX a user's experience

    NARCIS (Netherlands)

    Hanssen, F.T.Y.

    2003-01-01

    This paper presents a user's experience with installing fonts for use in LaTeX. It will be shown that it is not hard to make a standard Type 1 font work, if you use modern font installation software for LaTeX. All the steps necessary to install the example fonts will be shown. The example fonts used

  17. Drying of latex films and coatings: Reconsidering the fundamental mechanisms

    DEFF Research Database (Denmark)

    Kiil, Søren

    2006-01-01

    ), latex particle size (500-600 nm), initial polymer volume concentration (19-47 vol.%), and molecular weight of latex polymer (not quantified). Simulations also demonstrate that the transition from a constant to a falling drying rate in all cases takes place when the polymer volume concentration...

  18. Latex allergy in Bozyaka Social Security Hospital workers, Turkey

    Institute of Scientific and Technical Information of China (English)

    Kose Sukran; MandIraclo(g)glu Aliye

    2004-01-01

    @@ Latex glove used in healthcare settings has risen dramatically since around 1987. The increased threat of contracting HIV, hepatitis B, and other infectious agents during the course of delivering health care to patients has created the need for barrier protection. 1 Studies have estimated that the prevalence of latex allergy in healthcare workers ranged from 2.9% up to 17%.2

  19. Mosquito larvicidal and silver nanoparticles synthesis potential of plant latex

    Directory of Open Access Journals (Sweden)

    H.P. Borase

    2014-08-01

    Full Text Available Silver nanoparticles (AgNPs were synthesized from the latex of the medicinally important plants Euphorbia milii, Euphorbia hirta, Ficus racemosa and Jatropha curcas. Synthesized AgNPs were characterized by UV-Vis spectrophotometry, scanning electron microscopy, energy dispersive X-ray analysis, X-ray diffraction, Fourier transformed infrared spectroscopy, particle size, and zeta potential analysis. Potency of latex and latex-synthesized AgNPs was evaluated against the 2nd and 4th instar larvae of Aedes aegypti and Anopheles stephensi. The lowest lethal concentration 50 (LC50 value among the different types of plant latex studied was observed for latex of E. milii (281.28±23.30 and 178.97±37.82 ppm, respectively against 2nd instar larvae of Ae. aegypti and An. stephensi. E. milii latex-synthesised AgNPs showed a high reduction in LC50 compared with its latex; i.e., 8.76±0.46 and 8.67±0.47 ppm, respectively, for 2nd instars of Ae. aegypti and An. stephensi. LC50 values of AgNPs synthesized using the latex of E. hirta, F. racemosa and J. curcas were lower than those of the latex of the respective plants; i.e., 10.77±0.53, 9.81±0.52, 12.06±0.60 and 8.79±0.51, 9.83±0.52, 9.60±0.51 ppm, respectively, for 2nd instars of An. stephensi and Ae. aegypti. Similarly, as compared with the plant latex, lower LC50 values were reported for latex-synthesized AgNPs against 4th instars of Ae. aegypt and An. stephensi. Results showed that all the types of plant latex investigated have the potential to convert silver nitrate into AgNPs showing a spectrum of potent mosquito larvicidal effects, indicating the possibility of further exploration of the bioefficacy of latex and latex-synthesized AgNPs against vectors of public health concerns.

  20. Perpendicularly Aligned, Anion Conducting Nanochannels in Block Copolymer Electrolyte Films

    Energy Technology Data Exchange (ETDEWEB)

    Arges, Christopher G.; Kambe, Yu; Suh, Hyo Seon; Ocola, Leonidas E.; Nealey, Paul F.

    2016-03-08

    Connecting structure and morphology to bulk transport properties, such as ionic conductivity, in nanostructured polymer electrolyte materials is a difficult proposition because of the challenge to precisely and accurately control order and the orientation of the ionic domains in such polymeric films. In this work, poly(styrene-block-2-vinylpyridine) (PSbP2VP) block copolymers were assembled perpendicularly to a substrate surface over large areas through chemical surface modification at the substrate and utilizing a versatile solvent vapor annealing (SVA) technique. After block copolymer assembly, a novel chemical vapor infiltration reaction (CVIR) technique selectively converted the 2-vinylpyridine block to 2-vinyl n-methylpyridinium (NMP+ X-) groups, which are anion charge carriers. The prepared block copolymer electrolytes maintained their orientation and ordered nanostructure upon the selective introduction of ion moieties into the P2VP block and post ion-exchange to other counterion forms (X- = chloride, hydroxide, etc.). The prepared block copolymer electrolyte films demonstrated high chloride ion conductivities, 45 mS cm(-1) at 20 degrees C in deionized water, the highest chloride ion conductivity for anion conducting polymer electrolyte films. Additionally, straight-line lamellae of block copolymer electrolytes were realized using chemoepitaxy and density multiplication. The devised scheme allowed for precise and accurate control of orientation of ionic domains in nanostructured polymer electrolyte films and enables a platform for future studies that examines the relationship between polymer electrolyte structure and ion transport.

  1. Design of block copolymer membranes using segregation strength trend lines

    KAUST Repository

    Sutisna, Burhannudin

    2016-05-18

    Block copolymer self-assembly and non-solvent induced phase separation are now being combined to fabricate membranes with narrow pore size distribution and high porosity. The method has the potential to be used with a broad range of tailor-made block copolymers to control functionality and selectivity for specific separations. However, the extension of this process to any new copolymer is challenging and time consuming, due to the complex interplay of influencing parameters, such as solvent composition, polymer molecular weights, casting solution concentration, and evaporation time. We propose here an effective method for designing new block copolymer membranes. The method consists of predetermining a trend line for the preparation of isoporous membranes, obtained by computing solvent properties, interactions and copolymer block sizes for a set of successful systems and using it as a guide to select the preparation conditions for new membranes. We applied the method to membranes based on poly(styrene-b-ethylene oxide) diblocks and extended it to newly synthesized poly(styrene-b-2-vinyl pyridine-b-ethylene oxide) (PS-b-P2VP-b-PEO) terpolymers. The trend line method can be generally applied to other new systems and is expected to dramatically shorten the path of isoporous membrane manufacture. The PS-b-P2VP-b-PEO membrane formation was investigated by in situ Grazing Incident Small Angle X-ray Scattering (GISAXS), which revealed a hexagonal micelle order with domain spacing clearly correlated to the membrane interpore distances.

  2. In situ gelling stimuli-sensitive block copolymer hydrogels for drug delivery.

    Science.gov (United States)

    He, Chaoliang; Kim, Sung Wan; Lee, Doo Sung

    2008-05-08

    Stimuli-sensitive block copolymer hydrogels, which are reversible polymer networks formed by physical interactions and exhibit a sol-gel phase-transition in response to external stimuli, have great potential in biomedical and pharmaceutical applications, especially in site-specific controlled drug-delivery systems. The drug may be mixed with a polymer solution in vitro and the drug-loaded hydrogel can form in situ after the in vivo administration, such as injection; therefore, stimuli-sensitive block copolymer hydrogels have many advantages, such as simple drug formulation and administration procedures, no organic solvent, site-specificity, a sustained drug release behavior, less systemic toxicity and ability to deliver both hydrophilic and hydrophobic drugs. Among the stimuli in the biomedical applications, temperature and pH are the most popular physical and chemical stimuli, respectively. The temperature- and/or pH-sensitive block copolymer hydrogels for biomedical applications have been extensively developed in the past decade. This review focuses on recent development of the preparation and application for drug delivery of the block copolymer hydrogels that respond to temperature, pH or both stimuli, including poly(N-substituted acrylamide)-based block copolymers, poloxamers and their derivatives, poly(ethylene glycol)-polyester block copolymers, polyelectrolyte-based block copolymers and the polyelectrolyte-modified thermo-sensitive block copolymers. In addition, the hydrogels based on other stimuli-sensitive block copolymers are discussed.

  3. Bone substitute biomedical material of multi-(amino acid) copolymer: in vitro degradation and biocompatibility.

    Science.gov (United States)

    Li, Hong; Yan, Yonggang; Wei, Jie; Ma, Jian; Gong, Min; Luo, Xiaoman; Zhang, Yunfei

    2011-11-01

    Degradable polymers with good mechanical strength as bone repair biomaterials have been paid more attention in biomedical application. In this study, a multi-(amino acid) copolymer consisting of 6-aminocaproic acid and five natural amino acids was prepared by a reaction of acid-catalyzed condensation. The results revealed that the copolymer could be slowly degradable in Tris-HCl solution, and lost its initial weight of 31.9 wt% after immersion for 12 weeks, and the changes of pH value of Tris-HCl solution were in range from 6.9 to 7.4 during soaking. The compressive strength of the copolymer decreased from 107 to 68 MPa after immersion for 12 weeks. The proliferation and differentiation of MG-63 cells on the copolymer significantly increased with time, and the cells with normal phenotype extended and spread well on the copolymer surfaces. When the copolymer was implanted in muscle and bone defects of femoral cortex of dogs for 12 weeks, the histological evaluation confirmed that the copolymer exhibited excellent biocompatibility and more effective osteogenesis in vivo. When implanted into cortical bone defects of dogs, the copolymer could be combined directly with the natural bone without fibrous capsule tissue between implants and host bone. The results indicated that the multi-(amino acid) copolymer with sufficient strength, good biocompatibility and osteoconductivity had clinical potential for load-bearing bone repair or substitution.

  4. New co-polymer zwitterionic matrices for sustained release of verapamil hydrochloride.

    Science.gov (United States)

    Kostova, Bistra; Rachev, Dimitar

    2007-12-01

    Stable co-polymer [vinyl acetate-co-3-dimethyl(methacryloyloxyethyl) ammonium propane sulfonate, p(VA-co-DMAPS)] latex of different compositions has been synthesized for the first time by emulsifier-free emulsion copolymerization. The unusual >overshooting< behavior of the co-polymer tablets has been explained by the formation of specific clusters from the opposite oriented dipoles-zwitterionic species. The change of their concentration with the DMAPS unit fraction (mDMAPS), pH and ionic strength has been considered responsible for the differences observed in the swelling kinetics. The results obtained prove that mDMAPS and ionic strength could be used to control the swelling degree of the p(VA-co-DMAPS) matrices and their sustained drug delivery. In this way, p(VA-co-DMAPS) matrices could be effectively used to control the sustained release of drugs with basic properties like verapamil hydrochloride from model tablets.

  5. Polyphenoloxidase silencing affects latex coagulation in Taraxacum species.

    Science.gov (United States)

    Wahler, Daniela; Gronover, Christian Schulze; Richter, Carolin; Foucu, Florence; Twyman, Richard M; Moerschbacher, Bruno M; Fischer, Rainer; Muth, Jost; Prüfer, Dirk

    2009-09-01

    Latex is the milky sap that is found in many different plants. It is produced by specialized cells known as laticifers and can comprise a mixture of proteins, carbohydrates, oils, secondary metabolites, and rubber that may help to prevent herbivory and protect wound sites against infection. The wound-induced browning of latex suggests that it contains one or more phenol-oxidizing enzymes. Here, we present a comprehensive analysis of the major latex proteins from two dandelion species, Taraxacum officinale and Taraxacum kok-saghyz, and enzymatic studies showing that polyphenoloxidase (PPO) is responsible for latex browning. Electrophoretic analysis and amino-terminal sequencing of the most abundant proteins in the aqueous latex fraction revealed the presence of three PPO-related proteins generated by the proteolytic cleavage of a single precursor (pre-PPO). The laticifer-specific pre-PPO protein contains a transit peptide that can target reporter proteins into chloroplasts when constitutively expressed in dandelion protoplasts, perhaps indicating the presence of structures similar to plastids in laticifers, which lack genuine chloroplasts. Silencing the PPO gene by constitutive RNA interference in transgenic plants reduced PPO activity compared with wild-type controls, allowing T. kok-saghyz RNA interference lines to expel four to five times more latex than controls. Latex fluidity analysis in silenced plants showed a strong correlation between residual PPO activity and the coagulation rate, indicating that laticifer-specific PPO plays a major role in latex coagulation and wound sealing in dandelions. In contrast, very little PPO activity is found in the latex of the rubber tree Hevea brasiliensis, suggesting functional divergence of latex proteins during plant evolution.

  6. Preparation and application of comb-like fluorosilicon copolymer/nano silica hybrid%纳米SiO2杂化梳状氟硅共聚物的合成与性能研究

    Institute of Scientific and Technical Information of China (English)

    郝丽芬; 许伟; 安秋凤

    2015-01-01

    Comb- like perfluoroalkyl ester/trifluoropropyl/ethoxy silane containing polysiloxanes (FPFAS) in-termediate was prepared through hydrosilylation and ring- opening reaction, which was reacted with silica sols via in situ condensation to produce comb- like fluorosilicon copolymer/nano silica hybrid (FPFAS- SiO2). Super-hydrophobic cotton fabric with good soft handle and air permeability was fabricated via simple dip- coating method. IR, XPS, FESEM and contact angle tester were utilized to characterize its structure, morphology and application properties. The results indicated that the product had the due structure. Superhydrophobicity of the treated fabric was influenced by the particle diameter of nano silica. While mass concentration of the FP-FAS- SiO2 in ethyl acetate solution was 0.5%, water contact angle and rol- off angle on the treated fabric sur-face were 163.5° and 7°, respectively. The treated cotton fabric possessed favorable air permeability and soft-ness. A micro/nano multiscale composite film on the fiber surface could be clearly observed by FESEM.%用硅氢化加成和开环反应先制得梳状结构的全氟酯基/三氟丙基/硅乙氧基改性聚硅氧烷(FPFAS)中间体.然后利用硅乙氧基与硅溶胶间的原位缩合反应,制得了纳米SiO2梳状氟硅共聚物(FPFAS-SiO2).并用一步浸渍法处理棉织物构筑了兼具柔软、良好透气性的超疏水织物.用IR、XPS、FESEM、接触角测量仪等对产物结构、膜形貌及应用性能进行研究.结果表明,产物具有预期结构.纳米SiO2粒径影响织物的超疏水性能,当FPFAS-SiO2溶液用量为0.5%,整理后织物表面的水静态接触角和滚动角分别为163.5°和7°,具有良好的透气性和柔软性.FESEM可明显观察到纤维表面存在一层微/纳多尺度复合膜.

  7. Preparation and performance of soybean protein isolate-propylene glycol alginate-natural rubber latex%大豆分离蛋白-海藻酸丙二醇酯-天然乳胶共混膜的制备及性能研究

    Institute of Scientific and Technical Information of China (English)

    龚淑婷; 田晓慧; 孙金煜; 元以中

    2013-01-01

    采用杂凝聚法分别将大豆蛋白和海藻酸丙二醇酯与天然乳胶共混制备共混膜,红外光谱测试结果表明海藻酸丙二醇酯与大豆蛋白可形成共价复合物.通过对改性前后乳胶膜进行透射电镜、扫描电镜、原子力显微镜以及粒径分布测试,考察了大豆蛋白和海藻酸丙二醇酯对乳胶粒子形态及乳液固化成膜的影响.结果表明:适量添加大豆蛋白可增强膜的拉伸强度,当其固含量为0.83%时,共混改性膜的力学性能最优;进一步添加海藻酸丙二醇酯可较明显地提升断裂伸长率和拉伸强度,在其固含量为0.25%时,力学性能达到最大值;大豆蛋白和海藻酸丙二醇酯共混改性乳胶膜表面光滑度、致密性及力学性能均有所改善.%Blend films have been prepared by heterocoagulation blending of a mixture of soybean protein isolate (SPI) and propylene glycol alginate (PGA) in natural rubber latex (NRL). The particle morphology of NRL and the film formation process were studied by transmission electron microscopy (TEM) , scanning electron microscopy (SEM) and particle size distribution measurements. The SPI and PGA can form conjugates via the covalent attachment as indicated by the infrared spectra. The tensile strength was improved by addition of an appropriate amount of SPL The elongation at break was optimized when the loading of SPI was 0. 83% . However, the elongation at break of the films increased significantly after PGA loading, and the tensile strength also showed a small rise. When the loading of PGA was 0. 25% , the mechanical properties were optimized. The results show that the smoothness, compactness and mechanical properties of the membrane were all improved by addition of SPI-PGA conjugates.

  8. Nanostructured Polysulfone-Based Block Copolymer Membranes

    KAUST Repository

    Xie, Yihui

    2016-05-01

    The aim of this work is to fabricate nanostructured membranes from polysulfone-based block copolymers through self-assembly and non-solvent induced phase separation. Block copolymers containing polysulfone are novel materials for this purpose providing better mechanical and thermal stability to membranes than polystyrene-based copolymers, which have been exclusively used now. Firstly, we synthesized a triblock copolymer, poly(tert-butyl acrylate)-b-polsulfone-b-poly(tert-butyl acrylate) through polycondensation and reversible addition-fragmentation chain-transfer polymerization. The obtained membrane has a highly porous interconnected skin layer composed of elongated micelles with a flower-like arrangement, on top of the graded finger-like macrovoids. Membrane surface hydrolysis was carried out in a combination with metal complexation to obtain metal-chelated membranes. The copper-containing membrane showed improved antibacterial capability. Secondly, a poly(acrylic acid)-b-polysulfone-b-poly(acrylic acid) triblock copolymer obtained by hydrolyzing poly(tert-butyl acrylate)-b-polsulfone-b-poly(tert-butyl acrylate) formed a thin film with cylindrical poly(acrylic acid) microdomains in polysulfone matrix through thermal annealing. A phase inversion membrane was prepared from the same polymer via self-assembly and chelation-assisted non-solvent induced phase separation. The spherical micelles pre-formed in a selective solvent mixture packed into an ordered lattice in aid of metal-poly(acrylic acid) complexation. The space between micelles was filled with poly(acrylic acid)-metal complexes acting as potential water channels. The silver0 nanoparticle-decorated membrane was obtained by surface reduction, having three distinct layers with different particle sizes. Other amphiphilic copolymers containing polysulfone and water-soluble segments such as poly(ethylene glycol) and poly(N-isopropylacrylamide) were also synthesized through coupling reaction and copper0-mediated

  9. Synthesis and characterization of ferrocene containing block copolymers

    DEFF Research Database (Denmark)

    Chernyy, Sergey; Wang, Zhongli; Kirkensgaard, Jacob Judas Kain

    2017-01-01

    Narrowly dispersed diblock copolymers containing poly(methyl methacrylate) [PMMA] or poly(nonafluorohexyl methacrylate) [PF9MA] as the first block and poly(ferrocenylmethyl methacrylate) [PFMMA] as the second block, were prepared by anionic polymerization for the first time. Disordered bulk morph...

  10. Antiinflammatory Efficacy of Extracts of Latex of Calotropis procera Against Different Mediators of Inflammation

    Directory of Open Access Journals (Sweden)

    Soneera Arya

    2005-01-01

    Full Text Available The latex of the plant Calotropis procera has been reported to exhibit potent antiinflammatory activity against carrageenin and formalin that are known to release various mediators. In the present study, we have evaluated the efficacy of extracts prepared from the latex of C procera against inflammation induced by histamine, serotonin, compound 48/80, bradykinin (BK, and prostaglandin E(PGE in the rat paw oedema model. The paw oedema was induced by the subplantar injection of various inflammagens and oedema volume was recorded using a plethysmometer. The aqueous and methanol extracts of the dried latex (DL and standard antiinflammatory drugs were administered orally 1 hour before inducing inflammation. The inhibitory effect of the extracts was also evaluated against cellular influx induced by carrageenin. The antiinflammatory effect of aqueous and methanolic extracts of DL was more pronounced than phenylbutazone (PBZ against carrageenin while it was comparable to chlorpheniramine and PBZ against histamine and PGE, respectively. Both extracts produced about 80%, 40%, and 30% inhibition of inflammation induced by BK, compound 48/80, and serotonin. The histological analysis revealed that the extracts were more potent than PBZ in inhibiting cellular infiltration and subcutaneous oedema induced by carrageenin. The extracts of DL exert their antiinflammatory effects mainly by inhibiting histamine and BK and partly by inhibiting PGE.

  11. Development of a Specific Latex Agglutination Test to Detect Antibodies of Enterovirus 71.

    Science.gov (United States)

    Qin, Bo; Zhang, Jianhua; Xie, Wenhao; Liu, Xuehong; He, Tingting; Chen, Jinkun; Dong, Xuejun

    2015-10-01

    A latex agglutination test (LAT) was developed for the rapid detection of antibodies against the VP1 or VP1 proteins of Enterovirus 71 (EV71). The proteins of interest including prokaryotically expressed VP1 and two strains of anti-VP1 monoclonal antibody (McAb) against EV71 were covalently linked to carboxylated latex using ethyl-dimethyl-amino-propyl carbodiimide (EDC) to prepare sensitized latex beads. LAT was evaluated by an enzyme-linked immunosorbent assay (ELISA) as a reference test. The VP1-LAT showed a sensitivity of 87.0%, specificity of 88.9%, and an agreement ratio of 90.0% in detecting VP1 in 100 serum samples from experimentally infected mice, whereas these values were 86.8, 96.7, and 93.3%, respectively, for 608 clinical human serum samples. The VP1-LAT has advantages over other assays in terms of low cost, rapidity, chemical stability, high sensitivity, repeatability, and specificity. The LAT established in the present study is a rapid and simple test suitable for field monitoring of antibodies against VP1-EV71.

  12. Latex-mediated synthesis of ZnS nanoparticles: green synthesis approach

    Energy Technology Data Exchange (ETDEWEB)

    Hudlikar, Manish; Joglekar, Shreeram [University of Pune, Division of Biochemistry, Department of Chemistry (India); Dhaygude, Mayur [National Chemical Laboratory, Polymer Science and Engineering Division (India); Kodam, Kisan, E-mail: kodam@chem.unipune.ac.in [University of Pune, Division of Biochemistry, Department of Chemistry (India)

    2012-05-15

    A low-cost, green synthesis of ZnS nanoparticles is reported using 0.3 % latex solution prepared from Jatropha curcas L. ZnS nanoparticles were characterized by X-ray diffraction, selected area electron diffraction, transmission electron microscopy, energy dispersive analysis of X-rays, UV-vis optical absorption and photoluminescence techniques. Fourier Transform Infrared Spectroscopy was performed to find the role of cyclic peptides namely curcacycline A (an octapeptide), curcacycline B (a nonapeptide) and curcain (an enzyme) as a possible reducing and stabilizing agents present in the latex of J. curcas L. The average size of ZnS nanoparticles was found to be 10 nm. Latex of J. curcas L. itself acts as a source of sulphide (S{sup -2}) ions that are donated to Zn ions under present experimental conditions. Source of sulphide (S{sup -2}) ions is still unclear, but we speculate that cysteine or thiol residues present in enzyme curcain may be donating these sulphide (S{sup -2}) ions.

  13. Graft copolymers of polyurethane with various vinyl monomers via radiation-induced miniemulsion polymerization: Influential factors to grafting efficiency and particle morphology

    Energy Technology Data Exchange (ETDEWEB)

    Wang Hua [CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China (USTC), Hefei, Anhui 230026 (China); Wang Mozhen [CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China (USTC), Hefei, Anhui 230026 (China)], E-mail: pstwmz@ustc.edu.cn; Ge Xuewu [CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China (USTC), Hefei, Anhui 230026 (China)], E-mail: xwge@ustc.edu.cn

    2009-02-15

    Graft copolymers of polyurethane (PU) with various vinyl monomers were synthesized through a one-pot but two-step miniemulsion polymerization process. Firstly, the polycondensation of isophorone diisocyanate (IPDI) with hydroxyl-terminated polybutadiene (HTPB) had been performed in aqueous miniemulsion at 40 deg. C in order to obtain PU dispersions. Consecutively, an in-situ graft copolymerization of the vinyl monomers with the synthesized PU was initiated by {gamma}-ray radiation at room temperature. The grafting efficiency of PU with vinyl monomer (G{sub PU/monomer}) was calculated from {sup 1}H NMR spectra and the particle morphology of the final hybrid latex was observed by transmission electron microscopy (TEM). As there was no monomer transferring in miniemulsion system, homogenous hybrid particles would be synthesized provided that the monomer was miscible with PU, such as styrene. With the increase of the polarity of the monomer, the compatibility of PU with monomer decreased. G{sub PU/monomer} varied as G{sub PU/styrene}(37%)>G{sub PU/butyl} {sub acrylate} {sub (BA)}(21%)>G{sub PU/methyl} {sub methacrylate} {sub (MMA)}(12%). The proportion of homogeneous nucleation would increase as the hydrophilicity of the monomer increased. High temperature would destabilize the miniemulsion so as to result in a less grafting efficiency. Compared to the phase separation during the seeded emulsion polymerization, the miniemulsion polymerization method facilitated the preparation of homogeneous materials owing to its monomer droplet nucleation mechanism.

  14. Aqueous Tape Casting Process with Styrene-acrylic Latex Binder

    Institute of Scientific and Technical Information of China (English)

    CUI Xue-min; OUYANG Shi-xi; HUANG Yong; YU Zhi-yong; ZHAO Shi-ke; WANG Chang-an

    2004-01-01

    A commercial styrene-acrylic latex binder has been investigated as a good binder for aqueous Al2O3 suspensions tape-casting process. This paper focuses on the forming film mechanism of latex binder, the rheological behaviors of the suspensions, physical properties of green tapes and drying process of aqueous slurries with latex binder system. The drying process of the alumina suspensions is shown to follow a two-stage mechanism (the first stage: evaporation controlled process; and the second stage: diffusion controlled process). During the drying stage of the suspensions, the compressive force presses the latex particles and makes them be distorted, which results in cross-linking structure in contacted latex particles of the solidified tapes.A smooth-surface and high-strength green tape was fabricated by aqueous tape casting with latex binder system. The results from the SEM images of the crossing section microstructure of green tapes show that the latex is a very suitable binder for aqueous tape casting.

  15. The Synthesis and Modification of Nanosized Clickable Latex Particles

    KAUST Repository

    Almahdali, Sarah

    2013-05-01

    This research aims to add to the current knowledge available for miniemulsion polymerization reactions and to use this knowledge to synthesize multifunctional nanosized latex particles that have the potential to be used in catalysis. The physical properties of the latex can be adjusted to suit various environments due to the multiple functional groups present. For this research, styrene, pentafluorostyrene, azidomethyl styrene, pentafluorostyrene with azidomethyl styrene and pentafluorostyrene with styrene latexes were produced, and analyzed by dynamic light scattering. The latexes were synthesized using a miniemulsion polymerization technique found through this research. Potassium oleate and potassium 1,1,2,2,3,3,4,4-nonafluorobutane-1-sulfonate were used as surfactants during the miniemulsion polymerization reaction to synthesize pentafluorostyrene with azidomethyl styrene latex. Transmission electron microscopy data and dynamic light scattering data have been collected to analyze the structure of this latex, and it has been synthesized using a number of conditions, differing in reaction time, surfactant amount and sonication methods. We have also improved the solubility of the latex through a copper(I) catalyzed 1,3-dipolar azide-alkyne reaction, by clicking (polyethylene glycol)5000 onto the azide functional groups.

  16. New adhesive systems based on functionalized block copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Kent, M.; Saunders, R.; Hurst, M.; Small, J.; Emerson, J.; Zamora, D.

    1997-05-01

    The goal of this work was to evaluate chemically-functionalized block copolymers as adhesion promoters for metal/thermoset resin interfaces. Novel block copolymers were synthesized which contain pendant functional groups reactive toward copper and epoxy resins. In particular, imidazole and triazole functionalities that chelate with copper were incorporated onto one block, while secondary amines were incorporated onto the second block. These copolymers were found to self-assemble from solution onto copper surfaces to form monolayers. The structure of the adsorbed monolayers were studied in detail by neutron reflection and time-of-flight secondary ion mass spectrometry. The monolayer structure was found to vary markedly with the solution conditions and adsorption protocol. Appropriate conditions were found for which the two blocks form separate layers on the surface with the amine functionalized block exposed at the air surface. Adhesion testing of block copolymer-coated copper with epoxy resins was performed in both lap shear and peel modes. Modest enhancements in bond strengths were observed with the block copolymer applied to the native oxide. However, it was discovered that the native oxide is the weak link, and that by simply removing the native oxide, and then applying an epoxy resin before the native oxide can reform, excellent bond strength in the as-prepared state as well as excellent retention of bond strength after exposure to solder in ambient conditions are obtained. It is recommended that long term aging studies be performed with and without the block copolymer. In addition, the functionalized block copolymer method should be evaluated for another system that has inherently poor bonding, such as the nickel/silicone interface, and for systems involving metals and alloys which form oxides very rapidly, such as aluminum and stainless steel, where bonding strategies involve stabilizing the native oxide.

  17. 有机无机杂化物作乳化剂的苯丙乳液制备及其性能表征%Synthesis and Characterization of Poly(St-co-BA) Latex with an Organic-Inorganic Hybrid Compound as Emulsifier

    Institute of Scientific and Technical Information of China (English)

    袁俊杰; 周树学; 廖建和; 武利民

    2003-01-01

    A poly (St-co-BA) latex was successfully synthesized by using an organic-inorganic hybrid compound(OIHC), an aliphatic carboxylate sodium/nano-silica composite, as the emulsifier, and investigated by particlesize analyzer, transmission electron microscope (TEM), optical contact angle measurement (OCA) and dynamicmechanical analyzer (DMA). It was found that the protective agent, sodium polyacrylate (PA),could obviouslyimprove the polymerization stability and the functional monomer, glycidyl methacrylate (GMA), could enhancethe store stability of the latex. The particle size of poly(St-co-BA) latex decreased and then leveled off as OIHCcontent increased. TEM shows that the prepared polymers were actually organic-inorganic nanocomposites, andthese films have better waterproof property than those prepared by traditional poly(St-co-BA) latex or organicsilicone modified poly(St-co-BA) latex. The nanocomposite polymer has much higher glass transition temperaturethan organic silicone modified poly(St-co-BA) polymer containing the same organic silicone content.

  18. Synthesis, Micellization and Characterization of Novel Amphiphilic β-Cyclodextrin/Poly(L-aspartate) Copolymer

    Institute of Scientific and Technical Information of China (English)

    GUO Yan-ling; CUI Zhao-shan; HAN Min

    2013-01-01

    A novel amphiphilic β-cyclodextrin/poly(L-aspartate)(β-CD-PASP) copolymer was prepared by ringopening polymerization of polysuccinimide(PSI).This copolymer bears β-CD units along the macromolecular chain and the structure was characterized by infrared(IR) and proton nuclear magnetic resonance(1H NMR).The molecular weight of the copolymer was determined by gel permeation chromatography(GPC).The copolymer micelle were prepared by direct dissolution method.The critical micelle concentration(CMC) of the copolymer micelle was measured by flourescence technique with pyrene as probe.The size distribution of micelle was characterized on a dynamic laser light scattering particle size analyzer and its shape was observed by transmission electron microscopy(TEM).The results show that the copolymer could self-assemble into micelle with a low CMC,and the effective diameter of the micelle was 116.3 nm.The methotrexate(MTX)-loaded micelle were prepared and the drug loading content(DLC) was 22.86%.The MTX-loaded copolymer exhibited a better water-solubility than the free drug.

  19. [Successful desensitization to latex by sublingual immunotherapy in a health worker].

    Science.gov (United States)

    Bueno-De Sá, Adriano; Gaspar, Angela; Solé, Dirceu; Morais-Almeida, Mário

    2014-01-01

    Latex allergy is still a public health problem responsible for some occupational diseases tough to be treated without removing the patient from his/her workspace. For patients allergic to latex, sublingual immunotherapy (SLIT) for latex is a tool that can be very useful. We report the case of a nurse with latex allergy who underwent successful desensitization to latex by SLIT, and discuss about possible causes of the success of this therapy.

  20. Branched Rod-Coil Polyimide-Poly(Alkylene Oxide) Copolymers and Electrolyte Compositions

    Science.gov (United States)

    Meador, Maryann B. (Inventor); Tigelaar, Dean M. (Inventor)

    2014-01-01

    Crosslinked polyimide-poly(alkylene oxide) copolymers capable of holding large volumes of liquid while maintaining good dimensional stability. Copolymers are derived at ambient temperatures from amine endcapped amic-acid oligomers subsequently imidized in solution at increased temperatures, followed by reaction with trifunctional compounds in the presence of various additives. Films of these copolymers hold over four times their weight at room temperature of liquids such as ionic liquids (RTIL) and/or carbonate solvents. These rod-coil polyimide copolymers are used to prepare polymeric electrolytes by adding to the copolymers various amounts of compounds such as ionic liquids (RTIL), lithium trifluoromethane-sulfonimide (LiTFSi) or other lithium salts, and alumina.

  1. Solubility of dense CO2 in two biocompatible acrylate copolymers

    Directory of Open Access Journals (Sweden)

    A. R. C. Duarte

    2006-06-01

    Full Text Available Biocompatible polymers and copolymers are frequently being used as part of controlled delivery systems. These systems can be prepared using a "clean and environment friendly" technology like supercritical fluids. One great advantage of this process is that compressed carbon dioxide has excellent plasticizing properties and can swell most biocompatible polymeric matrixes, thus promoting drug impregnation processes. Mass sorption of two acrylate biocompatible copolymers contact with supercritical carbon dioxide is reported. Equilibrium solubility of dense carbon dioxide in poly(methylmethacrylate-co-ethylhexylacrylate and poly(methylmethacrylate-co-ethylhexylacrylate-co-ethyleneglycoldimethacrylate was studied by a static method at 10.0 MPa and 313 K. The reticulated copolymer had Fickean behavior and its diffusion coefficient was calculated, under operating conditions.

  2. Ordered nanoscale domains by infiltration of block copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Darling, Seth B.; Elam, Jeffrey; Tseng, Yu-Chih; Peng, Qing

    2016-11-08

    A method of preparing tunable inorganic patterned nanofeatures by infiltration of a block copolymer scaffold having a plurality of self-assembled periodic polymer microdomains. The method may be used sequential infiltration synthesis (SIS), related to atomic layer deposition (ALD). The method includes selecting a metal precursor that is configured to selectively react with the copolymer unit defining the microdomain but is substantially non-reactive with another polymer unit of the copolymer. A tunable inorganic features is selectively formed on the microdomain to form a hybrid organic/inorganic composite material of the metal precursor and a co-reactant. The organic component may be optionally removed to obtain an inorganic features with patterned nanostructures defined by the configuration of the microdomain.

  3. Functional Block Copolymers as Compatibilizers for Nanoclays in Polypropylene Nanocomposites

    DEFF Research Database (Denmark)

    Jankova Atanasova, Katja; Daugaard, Anders Egede; Stribeck, Norbert

    of Kraton L-1203 from Kuraray Co., Japan with molecular weight 7000 and PDI=1.05, and a hydrophilic block of quaternized dimethylaminoethyl methacrylate (DMAEMA). The size of the hydrophilic block was varied, which increasingly caused better dispersibility of the block copolymer in water. This was essential...... for the exchange of the Na+ ions of the used NCl (3.8 wt.-% aq. dispersion of montmorillonite, MMT from Laviosa Chimica Mineralia, Italy) by the synthesized charged block copolymer, which was performed in water. Modified nanoclays with 2.5 to 8.0 wt.-% of the quaternized PEB-b-PDMAEMA35 were prepared....... The exfoliation and intercalation was studied by XRD. Rheological measurements of either aq. solutions of the charged block copolymers or PP master batches with various amounts of the modified MMT were performed. Tensile tests of NCs show similar behaivor, but SAXS reveals change in the nanostructure. According...

  4. 歧化松香乙烯基酯单体及其与苯乙烯共聚材料的制备与性能*%Preparation and Properties of Disproportionated Rosin Vinyl Ester Monomer and Their Copolymer Materials with Styrene

    Institute of Scientific and Technical Information of China (English)

    杨雪娟; 李守海; 李梅; 黄坤; 夏建陵

    2013-01-01

    利用歧化松香和甲基丙烯酸缩水甘油酯为原料,通过环氧开环酯化反应制得了歧化松香甲基丙烯酸甘油二酯(DR-GMA)单体,然后加入一定量的反应型稀释剂苯乙烯制得DR-GMA单体/苯乙烯共聚材料。傅立叶变换红外分析表明,DR-GMA单体已经成功制备,制备的共聚材料中DR-GMA与苯乙烯已经完全共聚;扫描电子显微镜分析表明,苯乙烯和DR-GMA形成了较好的致密交联结构共聚物;弯曲性能测试表明,共聚材料具有一定的弯曲强度,其弯曲强度可达到11.92 MPa;动态热机械分析表明,共聚物具有较高的玻璃化转变温度,其玻璃化转变温度保持在90~110℃范围内;热重分析表明,共聚材料具有优异的热稳定性,其初始分解温度高达370℃。%Disproportionated rosin methyl acrylic acid diglyceride(DR-GMA) monomer was prepared via epoxy ring-opening esterification using disproportionated rosin and methyl acrylic glycidyl ester as raw materials. Then different concentration of reactive diluent styrene was added to prepare copolymerized materials. Fourier transform infrared spectroscopy analysis results demonstrate that target monomer has been successfully synthesized and styrene has almost entirely copolymerized with DR-GMA monomer. Scanning electron microscope analysis shows that styrene and DR-GMA form a homogeneous copolymerized system with good cross-linking structure. Flexural property test shows that the copolymer materials have relatively high flexural strength up to 11.92 MPa.Dynamic mechanical thermal analysis shows that the copolymers have high glass-transition temperatures ranged from 90℃to 110℃. Thermogravimetric analysis results demonstrate that the copolymer materials have excellent thermal stability,as all copolymers have a high thermal initial decomposition temperature at about 370℃.

  5. Comparative study on plant latex particles and latex coagulation in Ficus benjamina, Campanula glomerata and three Euphorbia species.

    Science.gov (United States)

    Bauer, Georg; Gorb, Stanislav N; Klein, Marie-Christin; Nellesen, Anke; von Tapavicza, Max; Speck, Thomas

    2014-01-01

    Among latex-producing plants, mainly the latex of Hevea brasiliensis has been studied in detail so far, while comprehensive comparative studies of latex coagulation mechanisms among the more than 20,000 latex-bearing plant species are lacking. In order to give new insights into the potential variety of coagulation mechanisms, the untreated natural latices of five latex-bearing plants from the families Euphorbiaceae, Moraceae and Campanulaceae were visualised using Cryo-SEM and their particle size compared using the laser diffraction method. Additionally, the laticifers of these plants species were examined in planta via Cryo-SEM. Similar latex particle sizes and shape were found in Ficus benjamina and Hevea brasiliensis. Hence, and due to other similarities, we hypothesize comparable, mainly chemical, coagulation mechanisms in these two species, whereas a physical coagulation mechanism is proposed for the latex of Euphorbia spp. The latter mechanism is based on the huge amount of densely packed particles that after evaporation of water build a large surface area, which accelerates the coagulation procedure.

  6. Comparative study on plant latex particles and latex coagulation in Ficus benjamina, Campanula glomerata and three Euphorbia species.

    Directory of Open Access Journals (Sweden)

    Georg Bauer

    Full Text Available Among latex-producing plants, mainly the latex of Hevea brasiliensis has been studied in detail so far, while comprehensive comparative studies of latex coagulation mechanisms among the more than 20,000 latex-bearing plant species are lacking. In order to give new insights into the potential variety of coagulation mechanisms, the untreated natural latices of five latex-bearing plants from the families Euphorbiaceae, Moraceae and Campanulaceae were visualised using Cryo-SEM and their particle size compared using the laser diffraction method. Additionally, the laticifers of these plants species were examined in planta via Cryo-SEM. Similar latex particle sizes and shape were found in Ficus benjamina and Hevea brasiliensis. Hence, and due to other similarities, we hypothesize comparable, mainly chemical, coagulation mechanisms in these two species, whereas a physical coagulation mechanism is proposed for the latex of Euphorbia spp. The latter mechanism is based on the huge amount of densely packed particles that after evaporation of water build a large surface area, which accelerates the coagulation procedure.

  7. Research on the Fracture Properties and Modification Mechanism of Polyester Fiber and SBR Latex Modified Cement Concrete

    Directory of Open Access Journals (Sweden)

    Mingkai Zhou

    2016-01-01

    Full Text Available Polyester fiber and SBR latex cement concrete is prepared as pavement surface material; its fracture properties including fracture toughness, fracture energy, CMOD, and flexural strength are studied comparing with those of normal concrete (NC, polyester fiber modified concrete (FMC, SBR polymer modified concrete (SMC, and the combination of polyester fiber and SBR polymer modified concrete (FSMC. The modification mechanism of the latex and fiber on the concrete was also studied by the methods including X-ray test, chemically combined water, heat of hydration, water loss, and scanning electron microscope. Results indicated that the concrete modified by latex and polyester fiber has flexural strength, fracture toughness, and fracture energy of 44.4%, 397.0%, and 462.8% higher than the reference normal concrete, the polymer retarded the hydration process and reduced the hydration degree of cement at early age, while the hydration degree is promoted by the polymer film for its excellent water resistance after 28 d, and the bond between the fiber and cement paste is improved by the latex.

  8. Effect of composite resin contamination with powdered and unpowdered latex gloves on its shear bond strength to bovine dentin.

    Science.gov (United States)

    Oskoee, S S; Navimipour, E J; Bahari, M; Ajami, A A; Oskoee, P A; Abbasi, N M

    2012-01-01

    The aim of the present study was to evaluate the effect of composite resin contamination with powdered and unpowdered latex gloves on the shear bond strength of etch-and-rinse and two-step self-etch adhesive systems. Standard flat dentin surfaces were prepared on the facial aspect of 120 bovine incisors and randomly assigned into two (n=60) groups: group 1: Single Bond (SB), group 2: Clearfil SE Bond (CSE). Furthermore, each group was randomly subdivided into three (n=20) based on the type of composite contamination (without contamination, contamination with powdered latex gloves, and contamination with unpowdered latex gloves). The adhesives were applied and resin composite bonded to the dentin. After thermocycling, the specimens were subjected to a shear bond strength test. Two-way analysis of variance (ANOVA) and a post hoc Bonferroni test were used for statistical analysis. One-way ANOVA was used to compare shear bond strength values in each group. Statistical significance was set at p composite surface contamination (p=0.001). In the SB group there were no significant differences between different surface treatments (p=0.08). In the CSE group a significant difference was observed between the subgroup without contamination and the subgroup with powdered latex glove contamination (p=0.01); however, no significant differences were observed between the other subgroups.

  9. Production of Gum from Cashew Tree Latex

    Directory of Open Access Journals (Sweden)

    O. S. AZEEZ

    2005-06-01

    Full Text Available This research is aimed at producing gum from cashew tree latex, which can act as substitute for gum Arabic. The method used include drying and size reduction of the exudates gum, sieving of the gum to remove impurities, dissolution of the gum in distilled water, filtration to remove polysaccharide waste and finally concentration and stability of the gum. Glycerine, starch and Zinc oxide are some of the additives used in stabilizing the gum. The pH and Viscosity on addition of various percentage concentration of stabilizing agent were determined. Gum of the best quality was obtained with viscosity and pH of 4.52 Ns/m2 and 4.2 respectively; this is because the natural pH of gum from Acacia Senegal ranges between 3.9 - 4.9. The gum can be used as an alternative for synthetic adhesive used presently for stamps and envelopes.

  10. Thermoresponsive latexes for fragrance encapsulation and release.

    Science.gov (United States)

    Popadyuk, N; Popadyuk, A; Kohut, A; Voronov, A

    2016-04-01

    To synthesize cross-linked latex particles protecting the encapsulated fragrance at ambient temperatures and facilitating the release of cargo at the temperature of the surface of the skin that varies in different regions of the body between 33.5 and 36.9°C. Poly(stearyl acrylate) (PSA), a polymer with long crystallizable alkyl side chains (undergoes order-disorder transitions at 45°C), was chosen as the main component of the polymer particles. As a result, new thermoresponsive polymer particles for fragrance encapsulation were synthesized and characterized, including assessing the performance of particles in triggered release by elevated temperature. To obtain network domains of various crystallinity, stearyl acrylate was copolymerized with dipropylene glycol acrylate caprylate (DGAC) (comonomer) in the presence of a dipropylene glycol diacrylate sebacate (cross-linker) using the miniemulsion process. Comonomers and a cross-linker were mixed directly in a fragrance during polymerization. Fragrance release was evaluated at 25, 31, 35 and 39°C to demonstrate a new material potential in personal/health care skin-related applications. Particles protect the fragrance from evaporation at 25°C. The fragrance release rate gradually increases at 31, 35 and 39°C. Two slopes were found on release plots. The first slope corresponds to a rapid fragrance release. The second slope indicates a subsequent reduction in the release rate. Crystalline-to-amorphous transition of PSA triggers the release of fragrances from cross-linked latex particles at elevated temperatures. The presence of the encapsulated fragrance, as well as the inclusion of amorphous fragments in the polymer network, reduces the particle crystallinity and enhances the release. Release profiles can be tuned by temperature and controlled by the amount of loaded fragrance and the ratio of comonomers in the feed mixture. © 2015 Society of Cosmetic Scientists and the Société Française de Cosmétologie.

  11. One-step routes from di- and triblock copolymer precursors to hydrophilic nanoporous poly(acrylic acid)-b-polystyrene

    DEFF Research Database (Denmark)

    Guo, Fengxiao; Jankova Atanasova, Katja; Schulte, Lars;

    2008-01-01

    Nanoporous polystyrene with hydrophilic pores was prepared from di- and triblock copolymer precursors. The precursor material was either a poly(tert-butyl acryl ate)-b-polystyrene (PtBA-b-PS) diblock copolymer synthesized by atom transfer radical polymerization (ATRP) or a polydimethylsiloxane......-b-poly(tertbutyl acrylate)-b-polystyrene (PDMS-b-PtBA-b-PS) triblock copolymer synthesized by a combination of living anionic polymerization and ATRP. In the latter copolymer, PS was the matrix and mechanically stable component, PtBA was converted by acidic deprotection to hydrophilic poly(acrylic acid) (PAA) providing...

  12. Preparation and Performance of β-Cyclodextrin Copolymers and Its Metal Complexes%β-环糊精共聚物及其金属配合物的制备与性能

    Institute of Scientific and Technical Information of China (English)

    姜彦; 靖玲; 郭海泉; 张洪文

    2012-01-01

    合成了顺丁烯二酸酐酯化β-环糊精与苯乙烯的共聚物及其金属配合物.利用红外、紫外、元素分析、差示扫描量热法及热失重分析法对其进行了结构表征和性能测试.这种含有β-环糊精的共聚物金属配合物作为脲酶抑制剂,对大豆脲酶催化尿素水解的抑制效果显著,其铜金属配合物为4 g/L时,抑制率达96.67%.%β-Cyclodextrin(β-CD) copolymers and its metal complexes were synthesized via the polymerization between (6-O-butene diacid ester) -β-cyclodextrin and styrene. Their structures and properties were characterized by infrared spectrum ( IR) , ultraviolet spectrum ( UV ) , elemental analysis ( EA ) , differential scanning calorimeter( DSC ) and thermogravimetry ( TG). Β-CD copolymers metal complexes used as urease inhibitors were investigated and showed prominent inhibition efficacy. The inhibition ratio of copolymer-Cu2 + complex was 96. 67% with a loading of 4 g/L.

  13. Triblock copolymers based on epsilon-caprolactone and trimethylene carbonate for the 3D printing of tissue engineering scaffolds

    NARCIS (Netherlands)

    Guney, Aysun; Malda, Jos; Dhert, Wouter J. A.; Grijpma, Dirk W.

    Background: Biodegradable PCL-b-PTMC-b-PCL triblock copolymers based on trimethylene carbonate (TMC) and epsilon-caprolactone (CL) were prepared and used in the 3D printing of tissue engineering scaffolds. Triblock copolymers of various molecular weights containing equal amounts of TMC and CL were

  14. Maleic anhydride based copolymer dispersions for surface modification of polar substrates

    NARCIS (Netherlands)

    Gunbas, I.D.; Wouters, M.E.L.; Hendrix, M.M.R.M.; Benthem, R.A.T.M. van; Koning, C.E.; Noordover, B.A.J.

    2012-01-01

    In this article, we report the modification of poly(styrene-alt-maleic anhydride) (PSMA) with monofunctional amine-terminated poly(dimethyl siloxane) (PDMS-NH2) by thermal imidization, followed by the preparation and characterization of a surfactant-free artificial latex thereof and application of t

  15. Maleic anhydride based copolymer dispersions for surface modification of polar substrates

    NARCIS (Netherlands)

    Gunbas, I.D.; Wouters, M.E.L.; Hendrix, M.M.R.M.; Benthem, R.A.T.M. van; Koning, C.E.; Noordover, B.A.J.

    2012-01-01

    In this article, we report the modification of poly(styrene-alt-maleic anhydride) (PSMA) with monofunctional amine-terminated poly(dimethyl siloxane) (PDMS-NH2) by thermal imidization, followed by the preparation and characterization of a surfactant-free artificial latex thereof and application of

  16. Ultrasound responsive block copolymer micelle of poly(ethylene glycol)-poly(propylene glycol) obtained through click reaction.

    Science.gov (United States)

    Li, Fayong; Xie, Chuan; Cheng, Zhengang; Xia, Hesheng

    2016-05-01

    The well-defined amphiphilic poly(ethylene glycol)-block-poly(propylene glycol) copolymer containing 1, 2, 3-triazole moiety and multiple ester bonds (PEG-click-PPG) was prepared by click reaction strategy. The PEG-click-PPG copolymer can self-assemble into spherical micelles in aqueous solution. It is found that high intensity focused ultrasound (HIFU) can open the copolymer PEG-click-PPG micelles and trigger the release of the payload in the micelle. The multiple ester bonds introduced in the junction point of the copolymer chain through click reactions were cleaved under HIFU, and leads to the disruption of the copolymer micelle and fast release of loaded cargo. The click reaction provides a convenient way to construct ultrasound responsive copolymer micelles with weak bonds. Copyright © 2015. Published by Elsevier B.V.

  17. Latex Dipping Machine PLC Control and Its Programming

    Directory of Open Access Journals (Sweden)

    Yimin Zhang

    2012-10-01

    Full Text Available Latex dipping machine is based on a latex patent products new-production condom and the development of the machine. The latex dipping agencies combined with production condom mechanism. First it realized a 3-dimensional accurate localization system using stepping motors. SIMATIC S7-200 series programmable controller, motion module EM253 and stepping motor are tied in wedlock to realize allocation of 3-dimension of X axis and Y axis and Z axis. Through the PTO pulse of Siemens S7-200 PLC controller and combined with the use of EM253 module, through the mould precise control programming soak glue and roll edge to achieve the control mold of rotation and swinging the uniform distributed latex. And the system has applied successfully in foreign-funded enterprise of Singapore.

  18. Ciprofloxacin Release Using Natural Rubber Latex Membranes as Carrier

    National Research Council Canada - National Science Library

    Dias Murbach, Heitor; Jaques Ogawa, Guilherme; Azevedo Borges, Felipe; Romeiro Miranda, Matheus Carlos; Lopes, Rute; Roberto de Barros, Natan; Guedes Mazalli, Alexandre Vinicius; Gonçalves da Silva, Rosângela; Ferreira Cinman, José Luiz; de Camargo Drago, Bruno; Donizetti Herculano, Rondinelli

    2014-01-01

      Natural rubber latex (NRL) from Hevea brasiliensis is easily manipulated, low cost, is of can stimulate natural angiogenesis and cellular adhesion, is a biocompatible, material and presents high mechanical resistance. Ciprofloxacin (CIP...

  19. Summary of appropriate measures to prevent natural rubber latex allergy

    Directory of Open Access Journals (Sweden)

    Xaver Baur

    1999-01-01

    Full Text Available This paper presents a short overview of the diagnostics and background of type I allergy to natural rubber latex proteins and makes recommendations for preventing corresponding allergic diseases in the future. These recommendations and prevention strategies are based on the current knowledge of latex allergy presented in the literature and are addressed to legislative bodies; manufacturers; directors of hospitals; those working at nursing facilities and physicians' and dentists' practices; as well as to other health service employees. Primary prevention is the focus but advice is also given on secondary prevention. The major preventive aim is the elimination of causative protein allergens in all latex devices and thus, the minimization of latex-related health problems.

  20. Coagulant and anticoagulant activities in Jatropha curcas latex.

    Science.gov (United States)

    Osoniyi, Omolaja; Onajobi, Funmi

    2003-11-01

    Jatropha curcas Linn. (Euphorbiaceae), a medicinal plant commonly grown in the Tropics, is traditionally used as a haemostatic. Investigation of the coagulant activity of the latex of Jatropha curcas showed that whole latex significantly (Platex, however, prolonged the clotting time: at high dilutions, the blood did not clot at all. This indicates that Jatropha curcas latex possesses both procoagulant and anticoagulant activities. Prothrombin time (PT) and activated partial thromboplastin time (APTT) tests on plasma confirm these observations. Solvent partitioning of the latex with ethyl acetate and butanol led to a partial separation of the two opposing activities: at low concentrations, the ethyl acetate fraction exhibited a procoagulant activity, while the butanol fraction had the highest anticoagulant activity. The residual aqueous fraction had no significant effect on the clotting time of blood and the PT but slightly prolonged the APTT.

  1. Tensile Strength of PHBV/Natural Rubber Latex Mixtures

    OpenAIRE

    Promkotra Sarunya; Kangsadan Tawiwan

    2015-01-01

    A polyhydroxybutyrate-co-hydroxyvalerate (PHBV) is mingled with natural rubber latex (R) to develop its mechanical property of the blend. Normally, substantial effects of the PHBV are hard, fragile, and inelastic, whereas the natural rubber is represented itself as very high elastic matter. The mixtures between the PHBV and natural rubber latex (R) are considered in different proportions. The PHBV solutions (w/v) are defined suitability at 1% (P1), 2% (P2), and 3% (P3). Their liquid mixtures ...

  2. A self-cleaning coating based on commercial grade polyacrylic latex modified by TiO{sub 2}/Ag-exchanged-zeolite-A nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Nosrati, Rahimeh, E-mail: ra.nosrati@gmail.com [Polymer Composite Research Laboratory, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of); Olad, Ali, E-mail: a.olad@yahoo.com [Polymer Composite Research Laboratory, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of); Nofouzi, Katayoon, E-mail: nofouzi@tabrizu.ac.ir [Faculty of Veterinary Medicine, University of Tabriz, Tabriz (Iran, Islamic Republic of)

    2015-08-15

    Graphical abstract: - Highlights: • A novel nanocomposite coating based on polyacrylic was prepared. • Nanostructured TiO{sub 2}/Ag-exchanged-zeolite-A composite material was prepared. • Prepared nanocomposite used as additive for modification of polyacrylic latex. • Modified coatings show self-cleaning and antibacterial properties. • Modified coatings show better stability in water in versus of unmodified polymer. - Abstract: The commercial grade polyacrylic latex was modified in order to prepare a self-cleaning coating. TiO{sub 2}/Ag-exchanged-zeolite-A nanocomposite was prepared and used as additive in the matrix of polyacrylic latex to achieve a hydrophilic and photocatalytic coating. FTIR and UV–visible spectroscopy, X-ray diffraction patterns and FESEM were used to characterize the composition and structure of the nanocomposites and coatings. The acrylic coatings, were prepared by using of TiO{sub 2}/Ag-exchanged-zeolite-A additive, had better UV and visible light absorption, hydrophilic, degradation of organic pollutants, stability in water and antimicrobial properties than pristine commercial grade polyacrylic latex coating. According to the results, the modified polyacrylic based coating containing 0.5 wt% of TiO{sub 2}/Ag-exchanged-zeolite-A nanocomposite additive with TiO{sub 2} to Ag-exchanged-zeolite-A ratio of 1:2 was the best coating considering most of useful properties such as small band gap and low water contact angle. The water contact angle for unmodified polyacrylic latex coating was 68° which was decreased to less than 10° in modified coating after 24 h LED lamp illumination.

  3. Immune response modulation by curcumin in a latex allergy model

    Directory of Open Access Journals (Sweden)

    Raju Raghavan

    2007-01-01

    Full Text Available Abstract Background There has been a worldwide increase in allergy and asthma over the last few decades, particularly in industrially developed nations. This resulted in a renewed interest to understand the pathogenesis of allergy in recent years. The progress made in the pathogenesis of allergic disease has led to the exploration of novel alternative therapies, which include herbal medicines as well. Curcumin, present in turmeric, a frequently used spice in Asia has been shown to have anti-allergic and inflammatory potential. Methods We used a murine model of latex allergy to investigate the role of curcumin as an immunomodulator. BALB/c mice were exposed to latex allergens and developed latex allergy with a Th2 type of immune response. These animals were treated with curcumin and the immunological and inflammatory responses were evaluated. Results Animals exposed to latex showed enhanced serum IgE, latex specific IgG1, IL-4, IL-5, IL-13, eosinophils and inflammation in the lungs. Intragastric treatment of latex-sensitized mice with curcumin demonstrated a diminished Th2 response with a concurrent reduction in lung inflammation. Eosinophilia in curcumin-treated mice was markedly reduced, co-stimulatory molecule expression (CD80, CD86, and OX40L on antigen-presenting cells was decreased, and expression of MMP-9, OAT, and TSLP genes was also attenuated. Conclusion These results suggest that curcumin has potential therapeutic value for controlling allergic responses resulting from exposure to allergens.

  4. Coalescing Aid Influences on Acrylic Latexes Property and Film Formation Process

    Directory of Open Access Journals (Sweden)

    Wang Yi

    2016-01-01

    Full Text Available The coalescing aid of propylene glycol phenyl ether (PPh influences on the latexes system and its film formation process have been demonstrated in this paper. The latexes with different Tg are synthesized by seeded semicontinuous emulsion polymerization. The PPh have a significant impact on the water evaporation stage, in which PPh decreased the water evaporation rate for a low Tg latex system but accelerated the rate for a high Tg latex. This result was quantified using Routh-Russel model which was a useful model for the prediction of the latex particle deformation mechanisms. The different amounts of PPh can change the latex particle deformation mechanisms. The TGA results show that the PPh still exist in the latexes films during drying. The microstructures of the latex film which dry under 70°C with the PPh for different time display that the PPh can accelerate the polymer molecules motion and the diffusion rate for the latex coalescence stage.

  5. Troubleshooting for the observed problems in processing latex concentrate from natural resource

    Science.gov (United States)

    Afreen, S.; Haque, K. R.; Huda, M. K.

    2013-06-01

    Natural latex has special importance in the rubber industry for manufacturing different types of goods like gloves, balloons, male contraceptive and similar thin walled articles. This natural latex is much more sensitive a liquid to handle since it can easily become contaminated and thereby coagulated which makes it unfavourable for centrifuge and getting concentrate from it. Some other related measures also are included in consideration during the processing of concentrate latex from the natural raw latex. The problems that are being faced in a concentrate latex processing plant can be categorized in different groups like, problems related to the latex property, mechanical problems, electrical problems, handling and storage problems, transformation problems, problems related to environmental issues, etc. Among them, the most common and vital problems frequently observed in a concentrate latex processing plant are discussed here with a view to finding the measures for solution which will help to maintain the latex property in any latex processing plant.

  6. Facile Fabrication of Water Dispersible Latex Particles with Homogeneous or Chain-Segregated Surface from RAFT Polymerization Using a Mixture of Two Macromolecular Chain Transfer Agents.

    Science.gov (United States)

    Sun, Li; Hong, Liangzhi; Wang, Chaoyang

    2016-04-01

    Water dispersible latex particles with randomly mixed shells or chain segregated surface are synthesized from one-pot reversible addition-fragmentation chain transfer heterogeneous polymerization of benzyl methacrylate (BzMA) using a mixture of poly(glycerol monomethacrylate) (PGMA) and poly(2,3-bis(succinyloxy)propyl methacrylate) (PBSPMA) macromolecular chain transfer agents. In methanol, the two in situ synthesized PGMA-b-PBzMA and PBSPMA-b-PBzMA diblock copolymers coaggregate into spherical micelles, which contain PBzMA core and discrete PGMA and PBSPMA nanodomains on the shell. In contrast, in water-methanol mixture (V/V = 9/1), latex particles with homogeneous distribution of PGMA and PBSPMA polymer chains on the shell are obtained. The reasons leading to formation of latex particles with homogenous or chain-segregated surface are discussed, and polymerization kinetics and physical state of PBSPMA in methanol and water-methanol mixtures are ascribed. These polymeric micelles with patterned functional group on the surface are potentially important for application in supracolloidal hierarchical assemblies and catalysis.

  7. Synthesis and properties of acrylic copolymers for ocular implants

    Science.gov (United States)

    Reboul, Adam C.

    There is a need for flexible polymers with higher refractive index and extended UV absorbing properties for improved intraocular lenses (IOLs). This research was devoted to the synthesis of new acrylic copolymers for foldable IOLs and to studies concerning IOL polymer properties. New polymers were synthesized from phenylated acrylates copolymerized with N-vinyl carbazole derivatives using bulk free radical addition methods. The copolymers had low Tg values, high refractive index, and were flexible. The N-vinyl carbazole derivatives were characterized by NMR and copolymers were characterized by DSC, UV-Vis, and refractometry. New phenothiazine based UV absorbers with high extinction coefficients were also synthesized for incorporation into ocular materials. Patent disclosures on UV absorbers and high refractive index polymers were prepared. A so called "glistening" phenomenon that occurs in all foldable intraocular lenses currently in clinical use is poorly understood and was studied. Research on this microvoid forming behavior included studies and development of methods to inhibit glistening in low Tg acrylic based copolymers. Glistenings were characterized using SEM and optical microscopy. A novel technique for inhibiting glistening was found and a patent disclosure was prepared.

  8. Bicontinuous Porous Carbon Films Templated with ABC Triblock Copolymers

    Science.gov (United States)

    Cavicchi, Kevin; Deng, Guodong; Vogt, Bryan

    2014-03-01

    Mesoporous carbons are useful for a range of applications such as separation and catalysis. A route to prepare porous materials is through cooperative self-assembly of a carbon precursor (e.g. phenolic resin) and a block copolymer, in which the precursor is selectively soluble, to drive mesophase formation. Typical soft templating uses AB or ABA block copolymers, which form classical morphologies, such as spheres, cylinders, and lamellae. Switching to an ABC type block copolymer provides greater flexibility in the design of the morphology potentially opening up larger processing windows for complex structures, such as bicontinuous morphologies. This presentation will discuss efforts to prepare bicontinuous porous carbon thin films using an ABC triblock copolymer of poly(ethylene oxide)-block-poly(ethyl acrylate)-block-polystyrene via spin-coating and a series of thermal annealing steps. It will be shown that direct thermal annealing can produce high porosity (~60%) carbon fiber networks. In addition, adding a solvent annealing step prior to the thermal annealing steps is able to produce longer range order structures with a small window of an ordered bicontinuous morphology. These high porosity films with organized fibers are promising for energy and separation applications.

  9. Non-random crosslinking of polysulphone-polysiloxane alternating block copolymers under irradiation

    Science.gov (United States)

    Xinfang, Chen; Chunshan, Zhang

    In this paper the effects of radiation on polysulphone-polysiloxane segmented copolymers have been investigated. The experimental observations indicate that the crosslinking reaction occurs primarily between siloxane segments and the intermolecular crosslinking of isopropylidene groups of adjacent polysulphone segments also takes place after the irradiation of higher doses. From the non-randon radiation crosslinking model which the block copolymer follows, the relationship between sol fraction and crosslink density is derived by a statistical method. The radiation crosslinking structure of block copolymers prepared by polycondensation of prepolymers, polysulphone and polysiloxane, can be controled by changing the average molecular weights of two prepolymers and the ratio of one component to the other.

  10. GRAFTED STYRENE-DIVINYLBENZENE COPOLYMERS CONTAINING BENZALDEHYDES AND THEIR WITTIG REACTIONS WITH VARIOUS PHOSPHONIUM SALTS

    Institute of Scientific and Technical Information of China (English)

    Adriana Popa; Gheorghe Ilia; Aurelia Pascariu; Smaranda Iliescu; Nicoleta Plesu

    2005-01-01

    A chloromethylated styrene-divinylbenzene copolymer support system functionalized with 4-benzaldehyde and 2-benzaldehyde was prepared. The degree of functionalization with aldehyde groups is well suited for the subsequent use of the products as Wittig reagents. The polymer bound aldehyde was reacted with Wittig reagents to give olefin groups grafted on styrene-divinylbenzene copolymers. The reactions were carried out in phase transfer catalysis conditions. A simple procedure for the calculation of the degree of functionalization and the statistical modeling of the structural repetitive unit of the copolymer are reported.

  11. SYNTHESIS AND CHARACTERIZATION OF REACTIVE GRAFT COPOLYMER PDMS-g- (PEO-OH)

    Institute of Scientific and Technical Information of China (English)

    QIU Yongxing; YU Xiaojie; FENG Lingxian

    1995-01-01

    A new reactive graft copolymer, poly (dimethyl siloxane)-graft-ω-hydroxyl-poly (ethylene oxide) (PDMS-g-(PEO-OH)), was synthesized by the hydrosilylation reaction of α, ω-bifunctional PEO macromonomer (CH2=CH-CH2-PEO-OH) with poly (hydromethylsiloxane) (PHMS). The obtained copolymer, exhibited the expected comblike structure as indicated by the result of detailed characterization and the needed reactivity as demonstrated by the result of esterification between PDMS-g-(PEO-OH)and aminoacetic acid. This reactive graft copolymer is expected to be very useful in the preparation of new bioactive polymer materials.

  12. Mechanically compliant electrodes and dielectric elastomers from PEG-PDMS copolymers

    DEFF Research Database (Denmark)

    A Razak, Aliff Hisyam; Madsen, Frederikke Bahrt; Skov, Anne Ladegaard

    2016-01-01

    Soft conducting elastomers have been prepared from polydimethylsiloxane-polyethyleneglycol (PDMS-PEG) copolymer and surfactant-stabilized multi-walled carbon nanotubes (MWCNTs). The copolymer was chain-extended with PDMS of molecular weight 17.2 kg mol-1 in order to obtain a crosslinkable PDMS...... showed high conductivity combined with inherent softness. The high conductivity and softness, PDMS-PEG copolymers with incorporated MWCNTs hold great promises as compliant and highly stretchable electrodes for stretchable devices such as electro-mechanical transducers....

  13. Preparation and properties of copolymer of graphene oxide and methyl acrylic acid and sodium methallyl sulfonate%氧化石墨烯与甲基丙烯酸和烯丙基磺酸钠共聚物的制备与性能∗

    Institute of Scientific and Technical Information of China (English)

    吕生华; 崔亚压; 杨文强; 周庆芳; 孙世彧

    2015-01-01

    The nanometer dispersion solution of graphene oxide (GO)was prepared by oxidation and ultrasoni-cation,followed carried out the free-radical copolymerization with methylacrylic acid (MAA)and sodium allyl-sulfonate (SAS)to synthesize the copolymer of GO,MAA and SAS (p(GO-MAA-SAS)).The copolymer was prepared by the weight ratios of MAA,SAS and GO of 1 3∶6∶1 .The FT-IR results indicated that the copoly-merization of GO and vinyl monomers was taken placed and GO naosheets were dispersed uniformly with thick-ness of 4 nm and size of 5-10 nm.The applied results indicated that the shrinkage temperature of the leather tanned with the 10% copolymer could reach 84 ℃,and the tanning function come from the synergistic effect of nano effects and functional groups.The research result has positive meaning to preparation of leather by green and clearning process.%通过氧化和超声波作用制备了氧化石墨烯(GO)纳米相片层分散液,再与甲基丙烯酸(MAA)和烯丙基磺酸钠(SAS)进行自由基共聚反应制备了氧化石墨烯与甲基丙烯酸和烯丙基磺酸钠的共聚物 P (GO-MAA-SAS),各组分的质量比为 m (MAA)∶m(SAS)∶m(GO)=13∶6∶1.FT-IR 检测结果表明GO 与单体之间发生了共聚反应,AFM检测结果表明共聚物中GO 片层的厚度为4 nm、长宽在5~10 nm范围.应用结果表明用10%的 P(GO-MAA-SAS)鞣制皮革的收缩温度为84℃,GO 的鞣制作用与 GO 的纳米效应和与胶原纤维的键合作用及其二者之间的协同作用有关,研究结果 GO 纳米片层可以鞣制皮革并且GO 的分散状态是影响鞣制效果的主要因素.

  14. Effect of molecular structure of aniline-formaldehyde copolymers on corrosion inhibition of mild steel in hydrochloric acid solution.

    Science.gov (United States)

    Zhang, Yan; Nie, Mengyan; Wang, Xiutong; Zhu, Yukun; Shi, Fuhua; Yu, Jianqiang; Hou, Baorong

    2015-05-30

    Aniline-formaldehyde copolymers with different molecular structures have been prepared and investigated for the purpose of corrosion control of mild steel in hydrochloric acid. The copolymers were synthesized by a condensation polymerization process with different ratios of aniline to formaldehyde in acidic precursor solutions. The corrosion inhibition efficiency of as-synthesized copolymers for Q235 mild steel was investigated in 1.0 mol L(-1) hydrochloric acid solution by weight loss measurement, potentiodynamic polarization, and electrochemical impedance spectroscopy, respectively. All the results demonstrate that as-prepared aniline-formaldehyde copolymers are efficient mixed-type corrosion inhibitors for mild steels in hydrochloric acid. The corrosion inhibition mechanism is discussed in terms of the role of molecular structure on adsorption of the copolymers onto the steel surface in acid solution.

  15. 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.

  16. SYNTHESIS, CHARACTERIZATION AND QUENCHING BEHAVIOR OF A CATIONIC POLY(p-PHENYLENEVINYLENE) RELATED COPOLYMER

    Institute of Scientific and Technical Information of China (English)

    Guang-wei Zhang; Qu-li Fan; Yan-qin Huang; Wei Huang

    2009-01-01

    A cationic poly(p-phenylene vinylene) related copolymer without bulky phenylene substitutents attached to the conjugated backbone was prepared through Wittig reaction. The molecular structure and optical properties were highly investigated through ~1H-NMR, UV and PL spectroscopy. The quenching behavior was also investigated, and the results demonstrate that incomplete quenching exists, which is consistent with the cationic poly(p-phenylene vinylene) related copolymer containing bulky phenylene substitutents, probably correlated with the conformation of conjugated backbone and intermolecular aggregation.

  17. Synthesis and Characterization of Chitosan-g-poly(D, L-lactic acid) Copolymer

    Institute of Scientific and Technical Information of China (English)

    Hua YANG; Shao Bing ZHOU; Xian Mo DENG

    2005-01-01

    Biodegradable chitosan-g-poly (D, L-lactic acid) copolymers were prepared via two methods. (1) The lactide was grafted onto hydroxyl groups of chitosan by using macromolecular initiator sodium of trimethylsilyl-chitosan, (2) poly (D,L-lactic acid)(PLA) with low molecular weight can be linked to the amino group by coupling activated PLA to trimethylsilyl-chitosan. Two graft copolymers had hydrophilic-hydrophobic character and can be applied as carriers for drug delivery.

  18. Synthesis and solution self-assembly of side-chain cobaltocenium-containing block copolymers.

    Science.gov (United States)

    Ren, Lixia; Hardy, Christopher G; Tang, Chuanbing

    2010-07-07

    The synthesis of side-chain cobaltocenium-containing block copolymers and their self-assembly in solution was studied. Highly pure monocarboxycobaltocenium was prepared and subsequently attached to side chains of poly(tert-butyl acrylate)-block-poly(2-hydroxyethyl acrylate), yielding poly(tert-butyl acrylate)-block-poly(2-acryloyloxyethyl cobaltoceniumcarboxylate). The cobaltocenium block copolymers exhibited vesicle morphology in the mixture of acetone and water, while micelles of nanotubes were formed in the mixture of acetone and chloroform.

  19. Synthesis and characterization of poly(phthalazinone ether nitrile)(PPEN)-polydimethylsiloxane (PDMS)block copolymers

    Institute of Scientific and Technical Information of China (English)

    Li Ming Dong; Gong Xiong Liao; Ming Jing Wang; Xi Gao Jian

    2008-01-01

    Block copolymers with different backbone compositions have been prepared by the condensation of dimethylamino terminated poly(dimethylsiloxane)(PDMS)and hydroquinone terminated poly(phthalazinone ether nitrile)(PPEN)in the presence of chlorobenzene/N-methyl pyrrolidone (NMP)as solvents.The products were characterized by FTIR,1H NMR and gel permeation chromatography.Differential scanning calorimetry analysis indicated that the block copolymers showed separated microphase.

  20. SYNTHESIS AND CHARACTERIZATION OF POLY(STYRENE—ETHYLENE OXIDE)DIBLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    GuoTianying; SongMoudao; 等

    1998-01-01

    Well-defined diblock copolymers of styrene(St) and ethylene oxide(EO) have been prepared by sequential living anionic polymerization of the two comonomers in THF.Diphenyl methyl potassum has been used as initiator.The block copolymers were characterized in detail by methods of size exclusion chromatography(SEC),1H-NMR,FT-IR,dynamic mechanical analysis(DMA) and WAXD.

  1. Synthesis and characterization of biodegradable materials: PDLLA-(MAh-Diol)n-PDLLA copolymer

    Institute of Scientific and Technical Information of China (English)

    Jia Chen; Yuan Liang Wang; Mei Na Huang

    2007-01-01

    The novel biodegradable copolymer PDLLA-(MAH-Diol)n-PDLLA with unsaturated bond was synthesized by copolymerizing lactide and prepolymer, which was prepared by the polycondensation of maleic anhydride and poly(ethylene glycol), using ptoluene sulphonic acid as catalyst. The new copolymer has improved hydrophilicity and flexibility. The structure and properties of the novel polymers were studied by FTIR, NMR, GPC-MALLS and DSC.

  2. Facile synthesis and characterization of novel biodegradable amphiphilic block copolymers bearing pendant hydroxyl groups

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Gaicen; Fan, Xiaoshan; Xu, Bingcan; Zhang, Delong; Hu, Zhiguo, E-mail: zghu@htu.cn

    2014-10-01

    Novel amphiphilic block copolymers bearing pendant hydroxyl groups polylactide-b–poly(3,3-bis(Hydroxymethyl–triazolylmethyl) oxetane)-b–polylactide (PLA-b–PHMTYO-b–PLA) were synthesized via a facile and efficient method. First, the block copolymer intermediates polylactide-b–poly(3,3-Diazidomethyloxetane)-b–polylactide (PLA-b–PBAMO-b–PLA) were synthesized through ring-opening polymerization of lactide using PBAMO as a macroinitiator. Following “Click” reaction of PLA-b–PBAMO-b–PLA with propargyl alcohol provided the targeted amphiphilic block copolymers PLA-b–PHMTYO-b–PLA with pendant hydroxyl groups. The composition and structure of prepared copolymers were characterized by {sup 1}H nuclear magnetic resonance ({sup 1}H NMR) spectroscopy, Fourier transform infrared (FT-IR) and gel permeation chromatography (GPC). The self-assembly behavior of the copolymers in water was investigated by transmission electron microscope (TEM), dynamic light scattering (DLS) and static light scattering (SLS). The results showed that the novel copolymers PLA-b–PHMTYO-b–PLA self-assembled into spherical micelles with diameters ranging from 100 nm to 200 nm in aqueous solution. These copolymers also exhibited low critical micellar concentrations (CMC: 6.9 × 10{sup −4} mg/mL and 3.9 × 10{sup −5} mg/mL, respectively). In addition, the in vitro cytotoxicity of these copolymers was determined in the presence of L929 cells. The results showed that the block copolymers PLA-b–PHMTYO-b–PLA exhibited better biocompatibility. Therefore, these well-defined copolymers are expected to find some applications in drug delivery or tissue engineering. - Highlights: • The method to synthesize PLA-b–PHMTYO-b–PLA is relatively facile and efficient. • PLA-b–PHMTYO-b–PLA self-assembles into spherical micelles with low CMC in water. • PLA-b–PHMTYO-b–PLA exhibits better biocompatibility and biodegradability.

  3. Latex glove allergy in dental workers: complications and predisposing factors

    Directory of Open Access Journals (Sweden)

    Rezaee M

    2007-11-01

    Full Text Available Background: Dermal- respiratory reactions to latex glove is a common problem and sometimes life threatening. Among health care workers, dental working personnel have extensive use of latex gloves. A few numbers of researches have been done in Iran about prevalence of these reactions but there is no comprehensive study for dental workers. The purpose of this study was to evaluate reactions to latex gloves amongst dental workers in military dental health centers.Methods: In this cross-sectional descriptive survey, dental workers with a minimum of three months length of employment and most often use of latex gloves were asked to fill standard questionnaire (derived from South Carolina Medical University regarding latex related clinical manifestation and personal medical history and predisposing factors Data analysis was done by χ2 and Student's t test.Results: In our study 330 personnel were assessed. The mean age and length of employment was 31.6 and 8 years respectively. The most occupation was dentistry. A total of 232 subjects (70.3% reported latex gloves-allergic symptoms. 72 (21.8% of persons have history of atopy and food allergy was seen in 114 (34.5%. 63 (19.1% of subjects reported history of hand dermatitis. All of these predisposing factors had positive regression with dermal and respiratory reactions.Conclusion: In this survey the prevalence of allergic reactions was higher than similar studies which may be due to type of gloves, lack of preemployment assessments and other factors. Use of diagnostic methods such as serologic measures, SPT and pulmonary function testing (such as spirogram could be considered as tools for confirmatory and differential diagnosis and important complementary for these studies. Because of relationship between allergic reactions to latex gloves and some medical histories, it seems to be necessary for preemployment evaluation and periodic health surveillance of dental workers.

  4. Antimicrobial activity of latex silver nanoparticles using Calotropis procera

    Institute of Scientific and Technical Information of China (English)

    Nadia; Hussein; Mohamed; Mady; Ahmed; Ismail; Wael; Moustfa; Abdel-Mageed; Ahmed; Abdelfattah; Mohamed; Shoreit

    2014-01-01

    Objective:To synthesize silver nanoparticles(AgNPs) by green methods using scrum latex of Calotropis procera at 80 ℃ and evaluate them against bacteria,dermatophytes and phytopathogenic fungi comparing with the activity of untreated latex.Methods:The synthesis of AgNPs was performed by mixing 3%latex scrum extract with the same volume of silver nitrate(2 mmol/L) solution in round flask and heating in water bath at80 ℃.Characterization of silver particles were determined using UV-vis spectrophotometer,transmission electron microscopy(TEM),X-ray diffraction and Fourier transform infrared spectroscopy.The antimicrobial activity of the green synthesized AgNPs was determined against bacteria,dermatophytes and phytopathogenic fungi and compared to the crude untreated latex by agar-well diffusion methods.Results:Biosynthesis of latex silver nanoparticles was successfully obtained by green method.The formation of AgNPs has been confirmed by UV-vis,TEM microscopy.X-ray diffraction and Fourier transform infrared spectroscopy.TEM analysis showed that synthesized AgNPs are highly stable spherical shaped particles,well dispersed with a diameter ranged from 4 nm up to 25 nm and an average size of 12.33 nm.AgNPs showed strong antibacterial activity against Gram-negative bacteria(Escherichia coli,Pseudomonas aeruginosa and Serratia sp.) and antifungal activity against Trichophyton rubrum,Candida albicans and Aspergillus terreus.Conclusions:It can be concluded that serum latex of Calotropis pmcera was found to display strong potential for the synthesis of AgNPs as antimicrobial agents through rapid reduction of silver ions(Ag~+ to Ag~0).The green synthesized AgNPs were found to show higher antimicrobial efficacy than crude latex.

  5. Antimicrobial activity of latex silver nanoparticles using Calotropis procera

    Institute of Scientific and Technical Information of China (English)

    Nadia Hussein Mohamed; Mady Ahmed Ismail; Wael Moustfa Abdel-Mageed

    2014-01-01

    Objective: To synthesize silver nanoparticles (AgNPs) by green methods using serum latex of Calotropis procera at 80 °C and evaluate them against bacteria, dermatophytes and phytopathogenic fungi comparing with the activity of untreated latex.Methods:The synthesis of AgNPs was performed by mixing 3% latex serum extract with the same volume of silver nitrate (2 mmol/L) solution in round flask and heating in water bath at 80 °C. Characterization of silver particles were determined using UV-vis spectrophotometer, transmission electron microscopy (TEM), X-ray diffraction and Fourier transform infrared spectroscopy. The antimicrobial activity of the green synthesized AgNPs was determined against bacteria, dermatophytes and phytopathogenic fungi and compared to the crude untreated latex by agar-well diffusion methods.Results:Biosynthesis of latex silver nanoparticles was successfully obtained by green method. The formation of AgNPs has been confirmed by UV-vis, TEM microscopy, X-ray diffraction and Fourier transform infrared spectroscopy. TEM analysis showed that synthesized AgNPs are highly stable spherical shaped particles, well dispersed with a diameter ranged from 4 nm up to 25 nm and an average size of 12.33 nm. AgNPs showed strong antibacterial activity against Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa and Serratia sp.) and antifungal activity against Trichophyton rubrum, Candida albicans and Aspergillus terreus.Conclusions:It can be concluded that serum latex of Calotropis procera was found to display strong potential for the synthesis of AgNPs as antimicrobial agents through rapid reduction of silver ions (Ag+ to Ag0). The green synthesized AgNPs were found to show higher antimicrobial efficacy than crude latex.

  6. Extraction and characterization of latex and natural rubber from rubber-bearing plants.

    Science.gov (United States)

    Buranov, Anvar U; Elmuradov, Burkhon J

    2010-01-27

    Consecutive extraction of latex and natural rubber from the roots of rubber-bearing plants such as Taraxacum kok-saghyz (TKS), Scorzonera tau-saghyz (STS), and Scorzonera Uzbekistanica (SU) were carried out. Latex extraction was carried via two methods: Blender method and Flow method. The results of latex extraction were compared. Cultivated rubber-bearing plants contained slightly higher latex contents compared to those from wild fields. Several creaming agents for latex extraction were compared. About 50% of total natural rubber was extracted as latex. The results of the comparative studies indicated that optimum latex extraction can be achieved with Flow method. The purity of latex extracted by Blender method ( approximately 75%) was significantly lower than that extracted by Flow method (99.5%). When the latex particles were stabilized with casein, the latex was concentrated significantly. Through concentrating latex by flotation, the latex concentration of 35% was obtained. Bagasse contained mostly solid natural rubber. The remaining natural rubber in the bagasse (left after the latex extraction) was extracted using sequential solvent extraction first with acetone and then with several nonpolar solvents. Solid natural rubber was analyzed for gel content and characterized by size exclusion chromatography (SEC) for molecular weight determinations. SEC of solid natural rubber has shown that the molecular weight is about 1.8E6 and they contain less gel compared to TSR20 (Grade 20 Technically Specified Rubber), a commercial natural rubber from Hevea brasiliensis.

  7. Aqueous-only, pH-induced nanoassembly of dual pKa-driven contraphilic block copolymers

    Science.gov (United States)

    Lee, Nam S.; Li, Yali; Ruda, C. Marcus

    2009-01-01

    pH-Responsive block copolymers, having two segments with functionalities of differing pKa, were prepared by NMP, providing a “green” route to the assembly of core/shell functionalizable nanostructures. PMID:18985203

  8. BARRIER PROPERTIES OF VINYLIDENE CHLORIDE COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    LI Yuesheng; WENG Zhixue; HUANG Zhiming; PAN Zuren

    1996-01-01

    The permeability coefficients of a series of copolymers of vinylidene chloride (VDC)with methyl acrylate (MA), butyl acrylate (BA) or vinyl chloride (VC) (as comonomer)to oxygen and carbon dioxide have been measured at 1.0 MPa and 30℃, while those to water vapor have been measured at 30℃ and 100% relative humidity. All the copolymers are semicrystalline. VDC/MA copolymers have lower melting temperature compared with VDC/BA copolymers, while that melting temperature of VDC/VC copolymer is higher than that of VDC/acrylate copolymers with the same VDC content. The barrier property of the copolymers is predominantly controlled by crystallite, free volume fraction, and cohesive energy. The permeability coefficients of VDC/MA copolymers to oxygen, carbon dioxide, and water vapor were successfully correlated with the ratio of free volume to cohesive energy.

  9. Comparative Analysis of Electromagnetic Response of PVA/MWCNT and Styrene-Acrylic Copolymer/MWCNT Composites

    Science.gov (United States)

    Plyushch, A. O.; Paddubskaya, A. G.; Kuzhir, P. P.; Maksimenko, S. A.; Ivanova, T.; Merijs-Meri, R.; Bitenieks, J.; Zicans, J.; Suslyaev, V. I.; Pletnev, M. A.

    2016-06-01

    The present paper focuses on electromagnetic response of polymeric composites with different concentrations of multiwall carbon nanotubes in the radio (20 Hz - 1 MHz) and microwave (26-36 GHz) frequency ranges. Widely available polymeric materials, such as PVA latex (polyvinyl acetate) and styrene-acrylic copolymer, were used as a matrix. Analysis of the experimental data demonstrated that in electromagnetic shielding applications one should give preference to the styrene-acrylic copolymer, as far as application of this matrix type allows reducing the percolation threshold in such composites. As a result, it allows reaching the necessary level of shielding at a lower filler concentration, while unique properties of the chosen polymer allow expanding the range of applications for the new materials.

  10. Purification, crystallization and preliminary X-ray analysis of CMS1MS2: a cysteine proteinase from Carica candamarcensis latex

    Science.gov (United States)

    Gomes, Marco Túlio Ribeiro; Teixeira, Raphael Dias; Ribeiro, Henrique de Assis Lopes; Turchetti, Andréia Pereira; Junqueira, Caroline Furtado; Lopes, Míriam Tereza Paz; Salas, Carlos Edmundo; Nagem, Ronaldo Alves Pinto

    2008-01-01

    Cysteine proteinases from the latex of plants of the family Caricaceae are widely used industrially as well as in pharmaceutical preparations. In the present work, a 23 kDa cysteine proteinase from Carica candamarcensis latex (designated CMS1MS2) was purified for crystallization using three chromatography steps. The enzyme shows about fourfold higher activity than papain with BAPNA as substrate. Crystals suitable for X-ray diffraction experiments were obtained by the hanging-drop method in the presence of PEG and ammonium sulfate as precipitants. The crystals are monoclinic (space group P21), with unit-cell parameters a = 53.26, b = 75.71, c = 53.23 Å, β = 96.81°, and diffract X-rays to 1.8 Å resolution. PMID:18540057

  11. Microwave assisted synthesis of fluorene-based copolymers with different conjugate degreed quinoxaline segments from reactive polymer

    Energy Technology Data Exchange (ETDEWEB)

    Li, Jixin; Song, Xiaohui; Feng, Ying [School of Petrochemical Engineering, Shenyang University of Technology, 30 Guanghua Street, Liaoyang 111003 (China); Wang, Zhiming, E-mail: wangzm2011@yahoo.com.cn [School of Petrochemical Engineering, Shenyang University of Technology, 30 Guanghua Street, Liaoyang 111003 (China); State Key Laboratory of Supramolecular Structure and Materials, Jilin University, 2699 Qianjin Avenue, Changchun 130012 (China); Zhang, Xiaojuan [School of Petrochemical Engineering, Shenyang University of Technology, 30 Guanghua Street, Liaoyang 111003 (China); Shen, Fangzhong; Lu, Ping [State Key Laboratory of Supramolecular Structure and Materials, Jilin University, 2699 Qianjin Avenue, Changchun 130012 (China)

    2013-10-31

    In this work, we prepared three fluorene-based copolymers with different conjugate degreed quinoxaline segments from one reactive polymer by microwave assisted method. The obtained quinoxaline-based copolymers exhibited different bright color emissions, high photoluminescence quantum, low electron affinity and electron injection barrier. This approach not only simplified the steps of similar-structure polymers, but also avoided the monomer solubility problem. - Highlights: • Quinoxaline-based copolymers were prepared in microwave-assisted synthesis. • Polymer-synthesis containing different acceptors was simplified from reactive polymer. • Multi-functions were tuned by controlling reactive monomer structures.

  12. Green engineered ZnO nanopowders by Banyan Tree and E. tirucalli plant latex: auto ignition route, photoluminescent and photocatalytic properties

    Science.gov (United States)

    Anilkumar, M. R.; Nagaswarupa, H. P.; Anantharaju, K. S.; Gurushantha, K.; Pratapkumar, C.; Prashantha, S. C.; Shashi Shekhar, T. R.; Nagabhushana, H.; Sharma, S. C.; Vidya, Y. S.; Prasad, Daruka

    2015-03-01

    A simple and eco-friendly solution combustion route was used to prepare ZnO nanoparticles (ZNPs) using Banyan Tree (BT) and Euphorbia tirucalli (ET) plant latexes as fuels. The final products were characterized by powder x-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), UV-visible, scanning electron microcopy (SEM) and transmission electron microscopy (TEM). The PXRD result reveals the formation of hexagonal phase with Wurtzite structure. The crystallite size obtained from TEM was found to be ˜20-25 nm. SEM results reveal rose-like morphology with BT latex and hexagonal shaped with ET latex. The energy band gap of ZNPs obtained by BT and ET latex were found to be 3.20 and 3.38 eV, respectively. Photoluminescence (PL) emission peaks at ˜421, 458, 505, 522, 628 and 695 nm were observed in both the samples when excited at 383 nm. These emission peaks were mainly attributed to deep level oxygen (blue-green) defect and exciton (UV) defects, respectively. The international commission on illumination (CIE) chromaticity co-ordinates, as well as co-ordinated color temperature (CCT), were estimated from the emission spectra; the values (x, y) were very close to national television system committee (NTSC) standard values of pure white emission. Photocatalytic activity (PCA) of ZNPs prepared was studied in detail. The ZNPs prepared using BT latex showed highest PCA under sunlight. The results demonstrate that the synthesized product could be quite useful for display applications as well as photocatalyst. Further, the material prepared by this route was found to be non-toxic, environmentally friendly and could be a potential alternative to economical routes.

  13. Investigating the rheological properties of native plant latex.

    Science.gov (United States)

    Bauer, Georg; Friedrich, Christian; Gillig, Carina; Vollrath, Fritz; Speck, Thomas; Holland, Chris

    2014-01-06

    Plant latex, the source of natural rubber, has been of interest to mankind for millennia, with much of the research on its rheological (flow) properties focused towards industrial application. However, little is known regarding the rheology of the native material as produced by the plant, a key factor in determining latex's biological functions. In this study, we outline a method for rheological comparison between native latices that requires a minimum of preparatory steps. Our approach provides quantitative insights into the coagulation mechanisms of Euphorbia and Ficus latex allowing interpretation within a comparative evolutionary framework. Our findings reveal that in laboratory conditions both latices behave like non-Newtonian materials with the coagulation of Euphorbia latex being mediated by a slow evaporative process (more than 60 min), whereas Ficus appears to use additional biochemical components to increase the rate of coagulation (more than 30 min). Based on these results, we propose two different primary defensive roles for latex in these plants: the delivery of anti-herbivory compounds (Euphorbia) and rapid wound healing (Ficus).

  14. The antigenotoxic activity of latex from Himatanthus articulatus

    Directory of Open Access Journals (Sweden)

    Sebastião de O. Rebouças

    2012-04-01

    Full Text Available Himatanthus articulatus (Vahl Woodson (Apocynaceae is a native plant to the Amazon popularly used to treat ulcers, tumors, inflammations, cancer, syphilis and malaria. The aim of the present study was to investigate the in vivo genotoxic/antigenotoxic and mutagenic potential of this plant, using the comet and the micronucleus assays in mice. Female and male adult mice were treated with different doses of H. articulatus latex by gavage for two consecutive days. For the experiments, the latex was serially diluted with water to 1:2 (D1; 1:4 (D½ and 1:8 (D¼ and administered to the animals. The blood slides were exposed to hydrogen peroxide (ex vivo to evaluate antigenotoxic effect. Under the experimental conditions used in this study, the latex of H. articulatus did not increase the frequency of DNA damage as measured by the comet assay and micronucleus test in treated mice, indicating a non-genotoxic and non-mutagenic activity. In relation to the antigenotoxicity, latex exerted protective effect against DNA damage induced by hydrogen peroxide. Therefore, our results add new information about the antigenotoxic potential of H. articulatus latex, which is popularly used in the Amazon to treat different pathologies.

  15. (Phenylen-carbazolylenes) copolymers: new soluble electroactive materials

    Energy Technology Data Exchange (ETDEWEB)

    Faid, K. (Lab. de Recherches sur les Macromolecules, Univ. Paris-Nord, 93 - Villetaneuse (France)); Ades, D. (Lab. de Recherches sur les Macromolecules, Univ. Paris-Nord, 93 - Villetaneuse (France)); Chevrot, C. (Lab. de Recherches sur les Macromolecules, Univ. Paris-Nord, 93 - Villetaneuse (France)); Siove, A. (Lab. de Recherches sur les Macromolecules, Univ. Paris-Nord, 93 - Villetaneuse (France))

    1993-03-22

    (Phenylen-Carbazolylenes) copolymers with tunable compositions and properties have been prepared by electrocatalyzed dehalogenative polycondensation of 4,4' dihalobiphenyl and 3,6-dibromo-N-alkylcarbazole mixtures in the presence of zero valent nickel catalyst. The polymers are partly soluble in polar solvents and this solubility depends on the proportion of carbazolylen units in the materials. For a given composition, it increases with the length of the aliphatic substituent on the nitrogen. The conductivity upon doping varies between those of the homopolymers and is a function of the length of the alkyl substituents. Thin films of these materials can be prepared either by solvent casting or by direct electrodeposition on various supports. The electrochemical behavior is strongly dependent on the copolymer composition and reveals the existence of two distinct electronic states (two quantum-wells). The first one is related to the presence of the carbazolylen units while the second shows the presence of phenylen moieties. (orig.)

  16. Electrosynthesis and study of phenylene-carbazolylene copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Faid, K. (Lab. de Recherches sur les Macromolecules, Univ. Paris Nord, 93 - Villetaneuse (France)); Ades, D. (Lab. de Recherches sur les Macromolecules, Univ. Paris Nord, 93 - Villetaneuse (France)); Siove, A. (Lab. de Recherches sur les Macromolecules, Univ. Paris Nord, 93 - Villetaneuse (France)); Chevrot, C. (Lab. de Recherches sur les Macromolecules, Univ. Paris Nord, 93 - Villetaneuse (France))

    1994-03-31

    Phenylene-carbazolylene copolymers with variable composition and properties were prepared by electrocatalyzed dehalogenative polycondensation of 4,4'-dihalobiphenyl and N-alkyl-3,6-dibromocarbazole mixtures in the presence of a zero valent nickel catayst. The polymers are partly soluble in polar solvents and this solubility depends on the proportion of carbazolylene units in the materials. For a given composition, solubility increases with length of the aliphatic substituent linked to the nitrogen. The conductivity upon doping varies between those of the corresponding homopolymers and is a function of the length of the alkyl substituents. Thin films of these materials can be prepared either by solvent casting or by direct electrodeposition onto various supports. The electrochemical behavior is strongly dependent on the copolymer composition and reveals the existence of two distinct electronic states (two quantum wells): the first one is related to the presence of the carbaxolylene units, while the second shows the presence of phenylene moieties. (orig.)

  17. Diffusion of oligomers in latex systems A route to low volatile organic compound (VOC) coatings

    National Research Council Canada - National Science Library

    Fasano, David M; Fitzwater, Susan J; Lau, Willie; Sheppard, Aurelia C

    2010-01-01

    We synthesize specially designed latex polymer systems by an in situ emulsion polymerization process that yields latex particles with both a high molecular weight polymer phase and a low molecular weight oligomer phase...

  18. The effects of temperature and pH bacterial degradation of latex ...

    African Journals Online (AJOL)

    The effects of temperature and pH bacterial degradation of latex paint in ... degradation of latex paint under humid condition by bacterial isolates was studied. ... can be preserved from bacterial contamination, deterioration and degradation by ...

  19. Micellization and Dynamics of a Block Copolymer

    DEFF Research Database (Denmark)

    Hvidt, Søren

    2006-01-01

    Triblock copolymers of the type EPE, where E and P denote ethylene oxide and propylene oxide blocks, respectively, are industrially important copolymers often called Pluronics or Poloxamers. EPE copolymers form micelles with a core of P blocks and different micellar shapes depending on block leng...

  20. Micellization and Dynamics of a Block Copolymer

    DEFF Research Database (Denmark)

    Hvidt, Søren

    2006-01-01

    Triblock copolymers of the type EPE, where E and P denote ethylene oxide and propylene oxide blocks, respectively, are industrially important copolymers often called Pluronics or Poloxamers. EPE copolymers form micelles with a core of P blocks and different micellar shapes depending on block length...

  1. Polypyrrole-coated styrene-butyl acrylate copolymer composite particles with tunable conductivity

    Institute of Scientific and Technical Information of China (English)

    HUANG Liyan; HOU Wenbo; LIU Zhengping; ZHANG Qingyue

    2005-01-01

    A series of near or monodisperse styrene-butyl acrylate (SBA) copolymer latex particles with different butyl acrylate contents were coated with polypyrrole. The structure of the SBA/PPy composites was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), X-ray photoelectron spectroscopy (XPS), differential scanning calorimetry (DSC) and standard four-probe method. The core-shell morphology of the SBA/PPy composite particles was confirmed. The result of DSC showed that Tg of the composite is mainly determined by the core component. The effects of the concentration of polypyrrole, the butyl acrylate content in SBA copolymer and the nature of the counter-anion on the electrical conductivity of compression-moulded samples were studied. It was first found that the electrical conductivity of the samples can be tuned by varying the butyl acrylate content in SBA copolymer and the highest conductivity of the core-shell composite was 0.17 S·cm-1.

  2. Anti-plasticizing effect of amorphous indomethacin induced by specific intermolecular interactions with PVA copolymer.

    Science.gov (United States)

    Ueda, Hiroshi; Aikawa, Shohei; Kashima, Yousuke; Kikuchi, Junko; Ida, Yasuo; Tanino, Tadatsugu; Kadota, Kazunori; Tozuka, Yuichi

    2014-09-01

    The mechanism of how poly(vinyl alcohol-co-acrylic acid-co-methyl methacrylate) (PVA copolymer) stabilizes an amorphous drug was investigated. Solid dispersions of PVA copolymer, poly(vinyl pyrrolidone) (PVP), and poly(vinyl pyrrolidone-co-vinyl acetate) (PVPVA) with indomethacin (IMC) were prepared. The glass transition temperature (Tg)-proportion profiles were evaluated by differential scanning calorimetry (DSC). General Tg profiles decreasing with the IMC ratio were observed for IMC-PVP and IMC-PVPVA samples. An interesting antiplasticizing effect of IMC on PVA copolymer was observed; Tg increased up to 20% IMC ratio. Further addition of IMC caused moderate reduction with positive deviation from theoretical values. Specific hydrophilic and hydrophobic interactions between IMC and PVA copolymer were revealed by infrared spectra. The indole amide of IMC played an important role in hydrogen bonding with PVA copolymer, but not with PVP and PVPVA. X-ray diffraction findings and the endotherm on DSC profiles suggested that PVA copolymer could form a semicrystalline structure and a possibility of correlation of the crystallographic nature with its low hygroscopicity was suggested. PVA copolymer was able to prevent crystallization of amorphous IMC through both low hygroscopicity and the formation of a specific intermolecular interaction compared with that with PVP and PVPVA.

  3. Effect of quaternary ammonium salts in the process of extracting oil filled rubber from latex

    Directory of Open Access Journals (Sweden)

    N. S. Nikulina

    2016-01-01

    Full Text Available Currently, much attention is paid to the improvement of production technology of synthetic rubber. Much attention is given to rubber is produced by emulsion polymerization. This is due to the fact that rubbers produced by emulsion polymerization have a number of positive characteristics, and are widely used in the tire and rubber industry, in composite formulations for various purposes. In recent years, the technology of production of synthetic rubbers are widely used quaternary ammonium salts which are produced on an industrial scale. Application low and high molecular weight quaternary ammonium salts to reduce pollution of environ-mental protection, exclude the use of mineral salts without significant changes in the process flowsheet. It is found that quaternary ammonium salts react with the components of the emulsion system to form insoluble complexes, which are captured produced rubber crumb. However, Applications, quaternary salts in the manufacture of oil-filled rubber in the literature sources have not been given due attention. The study presents the results of research on the effect of the concentration of a coagulating agent, tempera tours and concentration of the dispersed phase in the process of coagulation of latex in the preparation of oil-filled rubber stamps SCS-30 ARKM-15. The concentration of the coagulating agent does not significantly affect the process of separation of the rubber from the latex. The process of isolation rubber latex is advantageously carried out at a reduced temperature. The concentration of the dispersed phase also provides material effect on the coagulation process. The lead researches mouthestablished that produced rubber, rubber compounds and vulcanizates based on these indicators correspond to their requirements.

  4. Modification of isotactic polypropylene with styrene block-copolymers

    OpenAIRE

    DENAC, Matjaž; Musil, Vojko; Makarovič, Matjaž

    2015-01-01

    With a modification the current properties of polymeric material can be improved, and even some new properties can be obtained. The success of polymeric modifiers mostly depend on the interaction intensity at the phase boundary of the polymer/modifier. The influence of polymeric modifiers on polypropylene matrices were investigated. Different sorts and types of styrene block-copolymers were used in a concentration range up to 20 vol.%. Samples were prepared by melt-mixing in a Brabender knead...

  5. Studies on Gel Electrolyte Based on Nitrile-Butadiene Copolymers

    Science.gov (United States)

    1993-06-01

    preparation of a hybrid electrolyte, suitable for solid-polymer batteries. Based on the study of ionic conductivity in the presence of LiBF4 of a...lithium salts in different plasticizers showed the highest conductivity for LiBF4 . Conductivity of LiBF4 in different plasticizers decreases in the order...GLASS TRANSITION 53 TEMPERATURE OF VARIOUS NBR COPOLYMERS WITH AND WITHOUT LiBF4 APPENDIX B: ANOMALY IN THE IONIC 63 CONDUCTIVITY-TEMPERATURE STUDIES

  6. Caprine herpesvirus 1 (CpHV-1) vaginal infection of goats: clinical efficacy of fig latex.

    Science.gov (United States)

    Camero, Michele; Marinaro, Mariarosaria; Losurdo, Michele; Larocca, Vittorio; Bodnar, Livia; Patruno, Giovanni; Buonavoglia, Canio; Tempesta, Maria

    2016-01-01

    The latex of Ficus carica Linn. (Moraceae) has been shown to interfere with the replication of caprine herpesvirus (CpHV)-1 in vitro. The present study was undertaken to determine the efficacy of vaginal administration of fig latex in goats experimentally infected with CpHV-1. The fig latex reduced the clinical signs of the herpetic disease although it slightly influenced the titres of CpHV-1 shed. Thus, the fig latex maintained a partial efficacy in vivo.

  7. Latex sensitization and risk factors in female nurses in Thai governmental hospitals

    Directory of Open Access Journals (Sweden)

    Chompunuch Supapvanich

    2014-02-01

    Full Text Available Objectives: Exposure to latex allergens in latex gloves can cause occupational health problems in nurses, yet latex gloves are still widely used in Thai hospitals. Therefore, we conducted a study to determine the prevalence of latex sensitization in nurses and identify risk factors associated with sensitization. Methods: A questionnaire, providing information on personal characteristics, ill-health, working conditions and symptoms related to latex product use, was administered to 363 female nurses working in two tertiary hospitals in southern Thailand. Latex sensitization was confirmed using a solid phase immunoassay to detect anti-latex IgE antibodies. Total glove protein levels were determined by using a modified Lowry method and latex aeroallergens by a competitive inhibition immunoassay. Results: The overall prevalence of latex sensitization was 4.4%. Respiratory symptoms related to latex glove use were significantly associated with latex sensitization (OR = 5.5, 95% CI: 1.57-19. Total glove protein levels ranged 87.8-250.8 μg protein/dm2. The prevalence of latex sensiti- zation was higher (6.6% vs. 2.2% in the hospital where gloves with higher protein levels (82-438 μg/g vs. 86-170 μg/g were used. Furthermore, latex sensitization prevalence increased from 3% to 5% with increased average departmental aeroallergen concentrations. Conclusions: Latex sensitization prevalence in Thai nurses was higher than previously reported. Respiratory exposure seems to play an important role, in addition to dermal exposure. If latex gloves cannot be replaced by non-latex alternatives, replacement with gloves with lower protein content should be considered.

  8. Thin Films of Polydimethylsiloxane-Containing Block Copolymers

    Science.gov (United States)

    Wadley, Maurice; Cavicchi, Kevin

    2009-03-01

    The self-assembly of block copolymers into ordered nanostructures such as spheres, cylinders, and lamellae in the range of 10-100 nm makes them interesting materials for patterning surfaces. Thin films of poly(dimethylsiloxane) (PDMS) containing block copolymers are attractive for patterning due to their high oxygen etch resistance compared to other polymers. The main disadvantage of these polymers for patterning is the low surface tension of PDMS. This causes the preferential migration of PDMS to the air/film interface driving the formation of domains parallel to the interface and surface wetting layers. In this work a series of AB block copolymers containing PDMS have been prepared via RAFT polymerization where the surface tension of the opposing block was varied. Using a macro chain transfer approach, it is possible to isolate the effect of changing the opposing block while keeping the PDMS the same in each different block copolymer. The effect of changing the surface tension mismatch between the blocks on the thin film morphology will be discussed.

  9. Block copolymer-nanoparticle hybrid self-assembly

    KAUST Repository

    Hoheisel, Tobias N.

    2015-01-01

    © 2014 Published by Elsevier Ltd. Polymer-inorganic hybrid materials provide exciting opportunities as they may display favorable properties from both constituents that are desired in applications including catalysis and energy conversion and storage. For the preparation of hybrid materials with well-defined morphologies, block copolymer-directed nanoparticle hybrids present a particularly promising approach. As will be described in this review, once the fundamental characteristics for successful nanostructure formation at or close to the thermodynamic equilibrium of these nanocomposites are identified, the approach can be generalized to various materials classes. In addition to the discussion of recent materials developments based on the use of AB diblock copolymers as well as ABC triblock terpolymers, this review will therefore emphasize progress in the fundamental understanding of the underlying formation mechanisms of such hybrid materials. To this end, critical experiments for, as well as theoretical progress in the description of these nanostructured block copolymer-based hybrid materials will be discussed. Rather than providing a comprehensive overview, the review will emphasize work by the Wiesner group at Cornell University, US, on block copolymer-directed nanoparticle assemblies as well as their use in first potential application areas. The results provide powerful design criteria for wet-chemical synthesis methodologies for the generation of functional nanomaterials for applications ranging from microelectronics to catalysis to energy conversion and storage.

  10. Identification and characterization of Euphorbia nivulia latex proteins.

    Science.gov (United States)

    Badgujar, Shamkant B; Mahajan, Raghunath T

    2014-03-01

    The protein profile of latex of Euphorbia nivulia Buch.-Ham. is established. Three new proteins viz., Nivulian-I, II and III have been purified to homogeneity from the latex. The relative molecular masses of Nivulian-I, II and III are 31,486.985, 43,670.846 and 52,803.470 Da respectively. Nivulian-I is a simple type of protein while Nivulian-II and III are glycoproteins. Peptide mass fingerprint analysis revealed peptides of these proteins match with Tubulin alpha-1 chain of Eleusine indica, Maturase K of Banksia quercifolia and hypothetical protein of Zea mays respectively. Tryptic digestion profile of Nivulian-I, II and III, infer the exclusive nature of latex origin proteins and may be new and are additive molecules in the dictionaries of phytoproteins or botany. This is the first of its kind, regarding characterization and validation of Nivulian-I, II and III with respect to peptide sequencing.

  11. STUDY ON SYNTHESIS OF SELF CORSS LINKED POLYSTYRENE LATEX MICROSPHERES

    Institute of Scientific and Technical Information of China (English)

    DaiLizong; ZouYousi; 等

    1997-01-01

    Emulsifier-free emulsion polymerization of styrene in the presence of β-hydroxy propyl acrylate was studied.The emulsifier-free self cross linked polystyrene latex microspheres was obtained.Monomer conversion is higher than 90% when [St],[β-HPA],[KPS] is 2.66,0.228,and 5.8×10-3mol/L respectively under 80℃ for 5h.The mono-dispersed latex particle diameter and colloidal particle concentration were given as D=0.23um,N=3.13×1013/cm3 by TEM analyse,The factors of influencing latex stability were discussed.Thecopolymer was characterized by IR and dissolution experiment.The apparent activation energy of polymerization and polymerization rate constant were obtained to be 78.7KJ/mol and 514.4/mol.s respectively.

  12. GCMS analysis and antimicrobial action of latex of Euphorbia caducifolia

    Directory of Open Access Journals (Sweden)

    Manoj Goyal

    2012-04-01

    Full Text Available Euphorbia caducifolia is conspicuously and regularly represented in the flora of the Rajasthan state. Latex of E. caducifolia is used to cure skin infections, cutaneous eruption, leucoderma and applied to cuts and wounds for speedy healing. The GCMS analysis of fraction isolated from latex showed presence of methyl palmitate, 5,9-heptadecadienoate, methyl 11 octadecenoate, methyl octadecenoate and 3,7,11,15-tetramethyl- 2-hexadecene-l-ol. Isolated fraction of E. caducifolia (IFEC and latex of E. caducifolia (ECL were tested against S. aureus, M. luteus, B. subtilis, E. coli, S. typhi, A. niger and C. albicans. IFEC was found to be more effective against fungal species, and MIC was found to be 150 and micro;g/ml against A. niger. [J Intercult Ethnopharmacol 2012; 1(2.000: 119-123

  13. 40 CFR 428.110 - Applicability; description of the latex foam subcategory.

    Science.gov (United States)

    2010-07-01

    ... latex foam subcategory. 428.110 Section 428.110 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS RUBBER MANUFACTURING POINT SOURCE CATEGORY Latex Foam Subcategory § 428.110 Applicability; description of the latex foam subcategory. The provisions...

  14. IMMEDIATE AND DELAYED HYPERSENSITIVITY REACTIONS TO LATEX GLOVES IN A DENTAL STUDENT. A case report.

    Directory of Open Access Journals (Sweden)

    Iliyana Stoeva

    2011-08-01

    Full Text Available The article presents a case of dental student with immediate and delayed hypersensitivity reaction to latex gloves. Symptoms appeared during the second year of regularly using of latex gloves. The student was with no history of allergies and no previous exposure to latex products.

  15. Molecular detection of Papaya meleira virus in the latex of Carica papaya by RT-PCR

    NARCIS (Netherlands)

    Araujo, de M.M.M.; Tavares, E.T.; Silva, da F.R.; Marinho, V.L.D.; Souza, M.T.

    2007-01-01

    A RT-PCR assay was developed for early and accurate detection of Papaya meleira virus (PMeV) in the latex from infected papayas. The meleira disease is characterized by an excessive exudation of more fluidic latex from fruits, leaves and stems. This latex oxidises and gives the fruit a ¿sticky¿ text

  16. Proteomic analysis of latex from the rubber-producing plant Taraxacum brevicorniculatum

    NARCIS (Netherlands)

    Wahler, D.; Colby, T.; Kowalski, N.A.; Harzen, A.; Wotzka, S.Y.; Hillebrand, A.; Fischer, R.; Helsper, J.P.F.G.; Schmidt, J.; Schulze Gronover, C.; Prüfer, D.

    2012-01-01

    Many plants produce latex, a specialized, metabolically active cytoplasm. This is generally regarded as a defensive trait but latex may also possess additional functions. We investigated the role of latex in the dandelion species Taraxacum brevicorniculatum that contains considerable amounts of high

  17. 40 CFR 428.40 - Applicability; description of the latex rubber subcategory.

    Science.gov (United States)

    2010-07-01

    ... latex rubber subcategory. 428.40 Section 428.40 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS RUBBER MANUFACTURING POINT SOURCE CATEGORY Latex Rubber Subcategory § 428.40 Applicability; description of the latex rubber subcategory. The provisions...

  18. Science and technology of rubber reclamation with special attention to NR based waste latex products

    NARCIS (Netherlands)

    Rajan, V.V.; Dierkes, Wilma K.; Joseph, R.; Noordermeer, Jacobus W.M.

    2006-01-01

    A comprehensive overview of reclamation of cured rubber with special emphasis on latex reclamation is depicted in this paper. The latex industry has expanded over the years to meet the world demands for gloves, condoms, latex thread, etc. Due to the strict specifications for the products and the

  19. Morphology and film formation of poly(butyl methacrylate)-polypyrrole core-shell latex particles

    NARCIS (Netherlands)

    Huijs, F; Lang, J

    2000-01-01

    Core-shell latex particles made of a poly(butyl methacrylate) (PBMA) core and a thin polypyrrole (PPy) shell were synthesized by two-stage polymerization. In the first stage, PBMA latex particles were synthesized in a semicontinuous process by free-radical polymerization. PBMA latex particles were l

  20. Polyethylene-Based Tadpole Copolymers

    KAUST Repository

    Alkayal, Nazeeha

    2017-02-15

    Novel well-defined polyethylene-based tadpole copolymers ((c-PE)-b-PS, PE: polyethylene, PS: polystyrene) with ring PE head and linear PS tail are synthesized by combining polyhomologation, atom transfer radical polymerization (ATRP), and Glaser coupling reaction. The -OH groups of the 3-miktoarm star copolymers (PE-OH)-b-PS, synthesized by polyhomologation and ATRP, are transformed to alkyne groups by esterification with propiolic acid, followed by Glaser cyclization and removal of the unreacted linear with Merrifield\\'s resin-azide. The characterization results of intermediates and final products by high-temperature size exclusion chromatography, H NMR spectroscopy, and differential scanning calorimetry confirm the tadpole topology.