Non-woven PET fabric reinforced and enhanced the performance of ultrafiltration membranes composed of PVDF blended with PVDF-g-PEGMA for industrial applications

Science.gov (United States)

Wang, Shuai; Li, Tong; Chen, Chen; Chen, Sheng; Liu, Baicang; Crittenden, John

2018-03-01

Ultrafiltration (UF) membranes composed of poly(vinylidene fluoride) (PVDF) blended with poly(vinylidene fluoride)-graft-poly(ethylene glycol) methyl ether methacrylate (PVDF-g-PEGMA) can present high flux and excellent foulant removal efficiencies under suitable preparation conditions. However, these PVDF/PVDF-g-PEGMA blended membranes cannot be applied industrially because of the insufficient mechanical strength (strength-to-break value of 8.4 ± 0.6 MPa). We incorporated two types of non-woven polyethylene terephthalate (PET) fabrics (thin hydrophobic and thick hydrophilic fabrics) as support layers to improve the mechanical properties of the blended membranes. The thin and thick PET fabrics were able to significantly improve the tensile strength to 23.3 ± 3.7 MPa and 30.1 ± 1.4 MPa, respectively. The PET fabrics had a limited impact on the separation-related membrane performance such as hydrophilicity, foulant rejection, whereas the mechanical strength and pure water flux was improved several folds. The enhanced flux was attributed to the higher surface porosity and wider finger-like voids in the cross-section. The thin PET fabric with larger porosity was able to maintain a consistent toughness simultaneously; thus it is recommended as a support material for this blended membrane.

Impedance characteristics of nanoparticle-LiCoO{sub 2}+PVDF

Energy Technology Data Exchange (ETDEWEB)

Panjaitan, Elman, E-mail: elmanp@batan.go.id; Kartini, Evvy, E-mail: kartini@batan.go.id; Honggowiranto, Wagiyo [Center for Science and Technology for Advanced Materials, National Nuclear Energy Agency Kawasan Puspiptek Serpong, Tangerang Selatan15314 (Indonesia)

2016-02-08

The impendance of np-LiCoO{sub 2}+xPVDF, as a cathode material candidate for lithium-ion battery (LIB), has been characterized using impedance spectroscopy for x = 0, 5, 10, 15 and 20 volume percentage (%v/v) and for frequencies in the 42 Hz to 5 MHz range. Both real and imaginary components of the impedance were found to be frequency dependent, and both tend to increase for increasing PVDF (polyvinyilidene fluoride) concentration, except that for 10% PVDF both real and imaginary components of impedance are smaller than for 5%. The mechanism for relaxation time for each addition of PVDF was analyzed using Cole-Cole plots. The analysis showed that the relaxation times of the nanostructured LiCoO{sub 2} with PVDF additive is relatively constant. Further, PVDF addition increases the bulk resistance and decreases the bulk capacitance of the nanostructured LiCoO{sub 2}.

Improved high-frequency soft magnetic properties of FeCo films on organic ferroelectric PVDF substrate

Energy Technology Data Exchange (ETDEWEB)

Li, Dong; Wang, Zhen; Han, Xuemeng; Li, Yue; Guo, Xiaobin; Zuo, Yalu; Xi, Li, E-mail: xili@lzu.edu.cn

2015-02-01

FeCo films with various thicknesses were fabricated by direct-current magnetron sputtering on corning glass and organic ferroelectric PVDF substrates at the same time with 5 nm Ru seed layer and 5 nm Ta protective layer. The in-plane uniaxial anisotropy field of FeCo on glass substrate increases from 24 to 36 Oe with the increase of FeCo film thickness from 5 to 100 nm. However, a large in-plane anisotropy field of FeCo on PVDF substrate increases with FeCo thickness from 5 to 20 nm and gradually decreases with the FeCo thickness further increasing. Atomic force microscope images of FeCo on glass show quite smooth surface with root-mean-square roughness around 0.5 nm and have none visible granules on the surface for all samples. While, AFM images of FeCo on PVDF show quite rough surface with RMS roughness around 25 nm and have visible granules with the smallest granules appearing at the FeCo thickness of 20 nm. The permeability spectra show the typical ferromagnetic resonance phenomenon and can be well fitted by the LLG equation with the obtained experimental parameters. The ferromagnetic resonance frequency can reach 7.0 GHz for the 20 nm FeCo film on PVDF. Moreover, the quality factor of this sample can respectively reach 26, 12 and 7 at 1.0, 2.0, and 3.0 GHz, indicating the potential real 3G application for high-frequency devices. - Highlights: 1.Magnetic and morphological properties of FeCo films on PVDF substrates are studied. 2.The large anisotropy field of FeCo films on PVDF is obtained. 3.Improved high frequency properties of FeCo films on flexible substrates are obtained. 4.The origin of improved high frequency properties of FeCo films on PVDF is studied.

Graft copolymerization of N-vinyl-2-pyrrolidone onto pre-irradiated poly(vinylidene fluoride) powder

International Nuclear Information System (INIS)

Xu Chenqi; Huang Wei; Zhou Yongfeng; Yan Deyue; Chen Shutao; Huang Hua

2012-01-01

Graft copolymerization of N-vinyl-2-pyrrolidone (NVP) onto 60 Co γ-ray pre-irradiated poly (vinylidene fluoride) (PVDF) powder was investigated to find out the relationship between the degree of grafting (DG) and various factors, including monomer concentration, irradiation dose, reaction time, catalyst and so on. The DG can be calculated by comparing the amount of nitrogen element in the resulting copolymer (PVDF-g-PVP) powder with that in PVP on the basis of element analysis. The presence of PVP in the resulting PVDF powder was confirmed by the comparative studies of pristine PVDF and grafted PVDF powder through Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), thermo gravimetric analyzer (TGA) and differential scanning calorimetry (DSC), respectively. When the reaction was performed at the monomer concentration of 20% (vol.) and the absorbed dose of 40 kGy for 3 h in water, the max. DG of 17.7% was obtained. - Highlights: ► We modify pristine PVDF powders with NVP by the pre-irradiated graft polymerization. ► The various factors influencing the degree of grafting are investigated in detail. ► The optimal condition of graft polymerization is obtained. ► The polymerization is processed at 20% (vol.) of NVP and 40kGy for 3 hours in water. ► The maximum degree of grafting is 17.7 % at such a condition.

Effect of crosslinking on the physico-chemical properties of radiation grafted PEM fuel cell membranes

International Nuclear Information System (INIS)

Mohamed Mahmoud Nasef; Hamdani Saidi

2006-01-01

The effect of crosslinking on the physico-chemical properties of radiation grafted proton conducting membranes (PFA-g-PSSA) was investigated. The membranes were prepared by radiation induced grafting of styrene/divinylbenzene (DVB) mixtures onto poly (tetrafluoroethylene-co-perfluorovinyl either) (PFA) films followed by sulfonation reactions. The variation of DVB content in the grafting mixture was in the range of 1-4 vol %. The equivalent weight, swelling, behavior and the proton conductivity of crosslinked membranes having equal degrees of grafting prepared found to be dependent predominantly on the level of crosslinking. The obtained membranes were found to posses a good combination of physico-chemical properties that is matching the commercial Nation 117 membranes

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.

Preparation and characterization of functional poly(vinylidene fluoride) (PVDF) membranes with ultraviolet-absorbing property

Science.gov (United States)

Dong, Li; Liu, Xiangdong; Xiong, Zhengrong; Sheng, Dekun; Lin, Changhong; Zhou, Yan; Yang, Yuming

2018-06-01

We first reported a strategy to prepare functional poly(vinylidene fluoride) (PVDF) membranes with excellent ultraviolet-absorbing property through chemically induced grafting. Herein, the polymerizable ultraviolet (UV) absorber 2-hydroxy-4-(3-methacryloxy-2-hydroxylpropoxy) benzophenone (BPMA) made by ourselves was grafted onto the PVDF chains that have been pretreated with tetraethylammonium hydroxide (TEAH) alkaline solution. Moreover, the effect of experiment conditions such as the alkali and monomer concentrations, alkali treatment time on the UV-absorbing property of the obtained PVDF-g-PBPMA membranes were studied in detail. The chemical structure of the modified membranes was confirmed by 1H NMR, FT-IR and XPS measurements. Meanwhile, the thermal and UV-absorbing properties were characterized by TGA, DSC and UV-Vis spectrophotometer, respectively. The results indicated that BPMA side chains were successfully introduced onto PVDF backbones. Most importantly, the obtained PVDF-g-PBPMA membranes exhibited excellent UV-absorbing property. The transmittance of UV light at 300 nm decreased to as low as 0.02% and the UV light below 388 nm could be completely absorbed by the PVDF-g-PBPMA membrane made under optimal condition.

Asymmetric polivinylidenfluoride (PVDF) radiation grafted membranes: Preparation and performance in reverse osmosis application

International Nuclear Information System (INIS)

Vigo, F.; Capannelli, G.; Uliana, C.; Munari, S.

1981-01-01

A new type of reverse osmosis membrane has been synthesized. Membranes were prepared starting from asymmetric PVDF films, obtained by the casting and gelation technique and modified by radiochemical grafting and sulphonation. These membranes were tested in an RO laboratory plant and their performances were determined as a function of preparative parameters. The influences of evaporation time and temperature grafting and solvents were investigated. These membranes exhibit permeabilities as high as 2000 1/m 2 d and sodium chloride rejections up to 70%. (orig.)

Improved surface property of PVDF membrane with amphiphilic zwitterionic copolymer as membrane additive

Energy Technology Data Exchange (ETDEWEB)

Li Jianhua, E-mail: jhli_2005@163.com [Institute of Biomedical and Pharmaceutical Technology and College of Chemistry and Chemical Engineering, Fuzhou University, Fuzhou 350001 (China); Li Mizi; Miao Jing; Wang Jiabin; Shao Xisheng [Institute of Biomedical and Pharmaceutical Technology and College of Chemistry and Chemical Engineering, Fuzhou University, Fuzhou 350001 (China); Zhang Qiqing, E-mail: zhangqiq@126.com [Institute of Biomedical and Pharmaceutical Technology and College of Chemistry and Chemical Engineering, Fuzhou University, Fuzhou 350001 (China) and Institute of Biomedical Engineering, Chinese Academy of Medical Science, Peking Union Medical College, Tianjin 300192 (China)

2012-06-15

An attempt to improve hydrophilicity and anti-fouling properties of PVDF membranes, a novel amphiphilic zwitterionic copolymer poly(vinylidene fluoride)-graft-poly(sulfobetaine methacrylate) (PVDF-g-PSBMA) was firstly synthesized by atom transfer radical polymerization (ATRP) and used as amphiphilic copolymer additive in the preparation of PVDF membranes. The PVDF-g-PSBMA/PVDF blend membranes were prepared by immersion precipitation process. Fourier transform infrared attenuated reflection spectroscopy (FTIR-ATR) and X-ray photoelectronic spectroscopy (XPS) measurements confirmed that PSBMA brushes from amphiphilic additives were preferentially segregated to membrane-coagulant interface during membrane formation. The morphology of membranes was characterized by scanning electron microscopy (SEM). Water contact angle measurements showed that the surface hydrophilicity of PVDF membranes was improved significantly with the increasing of amphiphilic copolymer PVDF-g-PSBMA in cast solution. Protein static adsorption experiment and dynamic fouling resistance experiment revealed that the surface enrichment of PSBMA brush endowed PVDF blend membrane great improvement of surface anti-fouling ability.

Improved surface property of PVDF membrane with amphiphilic zwitterionic copolymer as membrane additive

International Nuclear Information System (INIS)

Li Jianhua; Li Mizi; Miao Jing; Wang Jiabin; Shao Xisheng; Zhang Qiqing

2012-01-01

An attempt to improve hydrophilicity and anti-fouling properties of PVDF membranes, a novel amphiphilic zwitterionic copolymer poly(vinylidene fluoride)-graft-poly(sulfobetaine methacrylate) (PVDF-g-PSBMA) was firstly synthesized by atom transfer radical polymerization (ATRP) and used as amphiphilic copolymer additive in the preparation of PVDF membranes. The PVDF-g-PSBMA/PVDF blend membranes were prepared by immersion precipitation process. Fourier transform infrared attenuated reflection spectroscopy (FTIR-ATR) and X-ray photoelectronic spectroscopy (XPS) measurements confirmed that PSBMA brushes from amphiphilic additives were preferentially segregated to membrane-coagulant interface during membrane formation. The morphology of membranes was characterized by scanning electron microscopy (SEM). Water contact angle measurements showed that the surface hydrophilicity of PVDF membranes was improved significantly with the increasing of amphiphilic copolymer PVDF-g-PSBMA in cast solution. Protein static adsorption experiment and dynamic fouling resistance experiment revealed that the surface enrichment of PSBMA brush endowed PVDF blend membrane great improvement of surface anti-fouling ability.

Enchansing the Ionic Purity of Hydrophilic Channels by Blending Fully Sulfonated Graft Copolymers with PVDF Homopolymer

DEFF Research Database (Denmark)

Nielsen, Mads Møller; Ching-Ching Yang, Ami; Jankova Atanasova, Katja

2013-01-01

The influence of tuning the ionic content of membranes by blending, as opposed to varying the degree of sulfonation, is evaluated. Membranes of fully sulfonated poly(vinylidene fluoride-co-chlorotrifluoroethylene)-g-poly(styrene sulfonic acid) blended with PVDF were prepared and investigated...

Solvent and irradiation doses effects on the ion exchange capacity of sulfonated styrene grafted PVDF

International Nuclear Information System (INIS)

Ferreira, Henrique P.; Parra, Duclerc F.; Lugao, Ademar B.

2011-01-01

Polymers exhibiting ion exchange capacity are studied for many years due to their application in several fields, such as membranes for proton exchange fuel cells, filtration membranes, heavy ions recovery and artificial muscles and sensors. Radiation induced grafting followed by sulfonation is a well-known way to obtain ion exchange polymers. Fluorinated polymers are frequently used as polymeric matrix for grafting due to their excellent physicochemical properties. Radiation induced grafting of styrene into poly (vinylidene fluoride) (PVDF) by simultaneous method in 1:1 styrene/toluene or styrene/N,N-dimethylformamide solutions was studied. Irradiations were performed under nitrogen atmosphere, room temperature and at doses of 5, 10 and 20 kGy with dose rate of 5 kGy.h -1 from a 60 Co gamma source. After washing, grafted materials were sulfonated in 10% chlorosulfonic acid/1,2-dichloroethane solutions for 4 h at room temperature. Characterization shows that increasing irradiation dose corresponds to increases in the grafting yield (GY %) gravimetrically calculated and these different solvents shows different grafting behaviors. Toluene allows no more than 3 % of grafting while DMF allows up to 55 % of grafting in the same condition. Grafting in toluene solution occurs on the surface and in DMF solution it occurs in the bulk, as confirmed by SEM. Both irradiation doses and solvent used have direct effects in the ion exchange capacities (calculated after titrations). FT-IR spectra exhibit new peaks after grafting and after sulfonation, attributed to grafted monomer and sulfonic groups attached to the styrene. DSC shows differences in thermal behavior of the polymer before and after each step. (author)

Solvent and irradiation doses effects on the ion exchange capacity of sulfonated styrene grafted PVDF

Energy Technology Data Exchange (ETDEWEB)

Ferreira, Henrique P.; Parra, Duclerc F.; Lugao, Ademar B. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2011-07-01

Polymers exhibiting ion exchange capacity are studied for many years due to their application in several fields, such as membranes for proton exchange fuel cells, filtration membranes, heavy ions recovery and artificial muscles and sensors. Radiation induced grafting followed by sulfonation is a well-known way to obtain ion exchange polymers. Fluorinated polymers are frequently used as polymeric matrix for grafting due to their excellent physicochemical properties. Radiation induced grafting of styrene into poly (vinylidene fluoride) (PVDF) by simultaneous method in 1:1 styrene/toluene or styrene/N,N-dimethylformamide solutions was studied. Irradiations were performed under nitrogen atmosphere, room temperature and at doses of 5, 10 and 20 kGy with dose rate of 5 kGy.h{sup -1} from a {sup 60}Co gamma source. After washing, grafted materials were sulfonated in 10% chlorosulfonic acid/1,2-dichloroethane solutions for 4 h at room temperature. Characterization shows that increasing irradiation dose corresponds to increases in the grafting yield (GY %) gravimetrically calculated and these different solvents shows different grafting behaviors. Toluene allows no more than 3 % of grafting while DMF allows up to 55 % of grafting in the same condition. Grafting in toluene solution occurs on the surface and in DMF solution it occurs in the bulk, as confirmed by SEM. Both irradiation doses and solvent used have direct effects in the ion exchange capacities (calculated after titrations). FT-IR spectra exhibit new peaks after grafting and after sulfonation, attributed to grafted monomer and sulfonic groups attached to the styrene. DSC shows differences in thermal behavior of the polymer before and after each step. (author)

Highly Hydrophilic Polyvinylidene Fluoride (PVDF) Ultrafiltration Membranes via Postfabrication Grafting of Surface-Tailored Silica Nanoparticles

KAUST Repository

Liang, Shuai

2013-07-24

Polyvinylidene fluoride (PVDF) has drawn much attention as a predominant ultrafiltration (UF) membrane material due to its outstanding mechanical and physicochemical properties. However, current applications suffer from the low fouling resistance of the PVDF membrane due to the intrinsic hydrophobic property of the membrane. The present study demonstrates a novel approach for the fabrication of a highly hydrophilic PVDF UF membrane via postfabrication tethering of superhydrophilic silica nanoparticles (NPs) to the membrane surface. The pristine PVDF membrane was grafted with poly(methacrylic acid) (PMAA) by plasma induced graft copolymerization, providing sufficient carboxyl groups as anchor sites for the binding of silica NPs, which were surface-tailored with amine-terminated cationic ligands. The NP binding was achieved through a remarkably simple and effective dip-coating technique in the presence or absence of the N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC)/N-hydroxysuccinimide (NHS) cross-linking process. The properties of the membrane prepared from the modification without EDC/NHS cross-linking were comparable to those for the membrane prepared with the EDC/NHS cross-linking. Both modifications almost doubled the surface energy of the functionalized membranes, which significantly improved the wettability of the membrane and converted the membrane surface from hydrophobic to highly hydrophilic. The irreversibly bound layer of superhydrophilic silica NPs endowed the membranes with strong antifouling performance as demonstrated by three sequential fouling filtration runs using bovine serum albumin (BSA) as a model organic foulant. The results suggest promising applications of the postfabrication surface modification technique in various membrane separation areas. © 2013 American Chemical Society.

Preparation and characterization of amphiphilic copolymer PVDF-g-PMABS and its application in improving hydrophilicity and protein fouling resistance of PVDF membrane

Science.gov (United States)

Chen, Fengtao; Shi, Xingxing; Chen, Xiaobing; Chen, Wenxing

2018-01-01

A facile strategy to improve the hydrophilicity and the antifouling properties of poly(vinylidene fluoride) (PVDF) membranes, a functional monomer of 4-methacrylamidobenzenesulfonic acid (MABS), was designed and synthesized through the amidation reaction between 2-methylacryloyl chloride and sulfanilic acid. Utilizing PVDF and the obtained MABS as reaction monomers, a novel amphiphilic copolymer was firstly prepared by radical polymerization method. The resulting PVDF-g-PMABS was used as a hydrophilic additive in the fabrication of PVDF porous membranes via immersion precipitation process. The surface chemical compositions and structure morphologies of as-prepared blend membranes (PVDF-g-PMABS/PVDF) were characterized by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), respectively. Contact angle measurement and cross-flow permeation test were employed to evaluate the hydrophilicity and antifouling properties of the membranes. It was found that the blend membrane with 4 wt.% PVDF-g-PMABS exhibited a noticeable pure water flux (136.34 L m-2 h-1) and a remarkable flux recovery ratio (FRR) of 98.60% in comparison with the pristine PVDF membrane (63.37 L m-2 h-1 and 38.67%, respectively). The enhanced performance was attributed to the synergetic effects of the strong hydrogen bonding force and the electrostatic repulsion of sulfonic groups against the protein foulants.

A method to modify PVDF microfiltration membrane via ATRP with low-temperature plasma pretreatment

Energy Technology Data Exchange (ETDEWEB)

Han, Yu [School of Marine Science, Ningbo University, Fenghua Road 818, Ningbo, 315211 (China); Ningbo University of Technology, Fenghua Road 201, Ningbo, 315211 (China); Song, Shuijun [School of Marine Science, Ningbo University, Fenghua Road 818, Ningbo, 315211 (China); Zhejiang University of Science Technology, Liuhe Road 318, Hangzhou, 310023 (China); Lu, Yin, E-mail: luyin@nbu.edu.cn [School of Marine Science, Ningbo University, Fenghua Road 818, Ningbo, 315211 (China); Zhu, Dongfa [School of Marine Science, Ningbo University, Fenghua Road 818, Ningbo, 315211 (China)

2016-08-30

Highlights: • We report a simple method to modify hydrophobic PVDF modification membrane. • Surface modification of PVDF membrane via ATRP with plasma pre-treatment. • ATRP grafting of SBMA onto the PVDF membrane surface form PVDF-g-SBMA membrane. • PVDF-g-SBMA membrane shows superior antifouling properties and hydrophilic. - Abstract: The hydrophilic modification of a polyvinylidene fluoride (PVDF) microfiltration membrane via pretreatment with argon plasma and direct surface-initiated atom transfer radical polymerization (ATRP) was studied. Both modified and unmodified PVDF membranes were characterized by Fourier transform infrared spectroscopy (FTIR), water contact angle, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and pore size distribution measurements. FTIR and XPS spectra confirmed that sulfobetaine methacrylate (SBMA) had been grafted onto the membrane surface. The initial contact angle decreased from 87.0° to 29.8° and a water drop penetrated into the modified membrane completely in 8 s. The pore size distribution of the modified membrane exhibited a smaller mean value than that of the original membrane. The antifouling properties of the modified PVDF membrane were evaluated by a filtration test using bovine serum albumin (BSA) solution. The results showed that the initial flux of the modified membrane increased from 2140.1 L/m{sup 2} h to 2812.7 L/m{sup 2} h and the equilibrium flux of BSA solution increased from 31 L/m{sup 2} h to 53 L/m{sup 2} h.

A method to modify PVDF microfiltration membrane via ATRP with low-temperature plasma pretreatment

International Nuclear Information System (INIS)

Han, Yu; Song, Shuijun; Lu, Yin; Zhu, Dongfa

2016-01-01

Highlights: • We report a simple method to modify hydrophobic PVDF modification membrane. • Surface modification of PVDF membrane via ATRP with plasma pre-treatment. • ATRP grafting of SBMA onto the PVDF membrane surface form PVDF-g-SBMA membrane. • PVDF-g-SBMA membrane shows superior antifouling properties and hydrophilic. - Abstract: The hydrophilic modification of a polyvinylidene fluoride (PVDF) microfiltration membrane via pretreatment with argon plasma and direct surface-initiated atom transfer radical polymerization (ATRP) was studied. Both modified and unmodified PVDF membranes were characterized by Fourier transform infrared spectroscopy (FTIR), water contact angle, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and pore size distribution measurements. FTIR and XPS spectra confirmed that sulfobetaine methacrylate (SBMA) had been grafted onto the membrane surface. The initial contact angle decreased from 87.0° to 29.8° and a water drop penetrated into the modified membrane completely in 8 s. The pore size distribution of the modified membrane exhibited a smaller mean value than that of the original membrane. The antifouling properties of the modified PVDF membrane were evaluated by a filtration test using bovine serum albumin (BSA) solution. The results showed that the initial flux of the modified membrane increased from 2140.1 L/m"2 h to 2812.7 L/m"2 h and the equilibrium flux of BSA solution increased from 31 L/m"2 h to 53 L/m"2 h.

Preparation of antifouling ultrafiltration membranes via irradiation induced graft polymerization technique

International Nuclear Information System (INIS)

Deng Bo; Liu Zhognying; Lu Xiaofeng; Li Jingye; Yang Xuanxuan; Yu Ming; Zhang Bowu

2010-01-01

PVDF powders were irradiated in air at dose of 15 kGy by using gamma-rays. Macromolecular peroxides transformed from free radicals in the irradiated PVDF powders in air can be preserved for long-term at appropriate temperature stably. By mixing acrylic monomers with irradiated PVDF powders then the graft polymerization can be initiated by heating. Then a series of hydrophilic ultrafiltration (UF) membranes were fabricated by dissolving the PVDF-g-PAAc powders in the NMP under phase inversion method. The antifouling performances of UF membranes cast from virgin and grafted PVDF powders were compared. (authors)

The impact of the school-based Psychosocial Structured Activities (PSSA) program on conflict-affected children in Northern Uganda.

Science.gov (United States)

Ager, Alastair; Akesson, Bree; Stark, Lindsay; Flouri, Eirini; Okot, Braxton; McCollister, Faith; Boothby, Neil

2011-11-01

Children in northern Uganda have undergone significant psychosocial stress during the region's lengthy conflict. A Psychosocial Structured Activities (PSSA) program was implemented in 21 schools identified as amongst those most severely affected by conflict-induced displacement across Gulu and Amuru Districts. The PSSA intervention comprised a series of 15 class sessions designed to progressively increase children's resilience through structured activities involving drama, movement, music and art (with additional components addressing parental support and community involvement). Eight schools were selected by random quota sampling from those schools receiving the PSSA intervention. Two hundred and three children were identified in these schools as being scheduled to receive intervention, and were followed up 12 months later following engagement with PSSA activities. A comparison group comprised 200 children selected from schools that had met inclusion criteria for receipt of intervention, but were not scheduled for intervention coverage until later. Preliminary research used participatory focus group methodology to determine local indicators of child well-being as viewed by parents, teachers, and children respectively. Pre- and post- assessments focused on ratings for each child - by parents, teachers and children - with respect to these indicators. Significant increases in ratings of child well-being were observed in both intervention and comparison groups over a 12-month period. However, the well-being of children who had received the PSSA intervention increased significantly more than for children in the comparison group, as judged by child and parent (but not teacher) report. This effect was evident despite considerable loss-to-follow-up at post-testing as a result of return of many households to communities of origin. General improvement in child well-being over a 12-month period suggests that recovery and reconstruction efforts in Northern Uganda following

Design of poly(vinylidene fluoride)-g-p(hydroxyethyl methacrylate-co-N-isopropylacrylamide) membrane via surface modification for enhanced fouling resistance and release property

International Nuclear Information System (INIS)

Zhao, Guili; Chen, Wei Ning

2017-01-01

Highlights: • PVDF modified membranes were designed by grafting PNIPAAm, PHEMA and their copolymer. • Fouling resistance and release property of membrane were both improved after modification. • Bacterial attachment and detachment were investigated to evaluate fouling release property. • Improvement of the antifouling property was justified by surface property analysis. • The copolymer modified membrane exhibited higher performance to release foulant. - Abstract: Thermo-sensitive polymer poly(N-isopropylacrylamide) (PNIPAAm), hydrophilic polymer poly(hydroxyethyl methacrylate) (PHEMA) and copolymer p(hydroxyethyl methacrylate-co-N-isopropylacrylamide) [P(HEMA-co-NIPAAm)] were synthesized onto poly(vinylidene fluoride) (PVDF) membrane via atom transfer radical polymerization (ATRP) in order to improve not only fouling resistance but also fouling release property. The physicochemical properties of membranes including hydrophilicity, morphology and roughness were examined by contact angle analyzer, scanning electron microscopy (SEM), and atomic force microscopy (AFM), respectively. The antifouling property of membranes was improved remarkably after surface modification according to protein and bacterial adhesion testing, and filtration experiment. Minimum protein adsorption and bacterial adhesion were both obtained on PVDF-g-P(HEMA-co-NIPAAm) membrane, with reduction by 44% and 71% respectively compared to the pristine membrane. The minimum bacterial cells after detachment at 25 °C were observed on the PVDF-g-P(HEMA-co-NIPAAm) membrane with the detachment rate of 77%, indicating high fouling release property. The filtration testing indicated that the copolymer modified membrane exhibited high resistance to protein fouling and the foulant on the surface was released and removed easily by washing, suggesting high fouling release and easy-cleaning capacity. This study provides useful insight in the combined “fouling resistance” and “fouling release�

Design of poly(vinylidene fluoride)-g-p(hydroxyethyl methacrylate-co-N-isopropylacrylamide) membrane via surface modification for enhanced fouling resistance and release property

Energy Technology Data Exchange (ETDEWEB)

Zhao, Guili [Nanyang Environment and Water Research Institute, Interdisciplinary Graduate School, Nanyang Technological University, 1 Cleantech Loop, Singapore 637141 (Singapore); Advanced Environmental Biotechnology Centre, Nanyang Environment and Water Research Institute, Nanyang Technological University, 1 Cleantech Loop, Singapore 637141 (Singapore); School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, Singapore 637459 (Singapore); Chen, Wei Ning, E-mail: WNChen@ntu.edu.sg [School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, Singapore 637459 (Singapore)

2017-03-15

Highlights: • PVDF modified membranes were designed by grafting PNIPAAm, PHEMA and their copolymer. • Fouling resistance and release property of membrane were both improved after modification. • Bacterial attachment and detachment were investigated to evaluate fouling release property. • Improvement of the antifouling property was justified by surface property analysis. • The copolymer modified membrane exhibited higher performance to release foulant. - Abstract: Thermo-sensitive polymer poly(N-isopropylacrylamide) (PNIPAAm), hydrophilic polymer poly(hydroxyethyl methacrylate) (PHEMA) and copolymer p(hydroxyethyl methacrylate-co-N-isopropylacrylamide) [P(HEMA-co-NIPAAm)] were synthesized onto poly(vinylidene fluoride) (PVDF) membrane via atom transfer radical polymerization (ATRP) in order to improve not only fouling resistance but also fouling release property. The physicochemical properties of membranes including hydrophilicity, morphology and roughness were examined by contact angle analyzer, scanning electron microscopy (SEM), and atomic force microscopy (AFM), respectively. The antifouling property of membranes was improved remarkably after surface modification according to protein and bacterial adhesion testing, and filtration experiment. Minimum protein adsorption and bacterial adhesion were both obtained on PVDF-g-P(HEMA-co-NIPAAm) membrane, with reduction by 44% and 71% respectively compared to the pristine membrane. The minimum bacterial cells after detachment at 25 °C were observed on the PVDF-g-P(HEMA-co-NIPAAm) membrane with the detachment rate of 77%, indicating high fouling release property. The filtration testing indicated that the copolymer modified membrane exhibited high resistance to protein fouling and the foulant on the surface was released and removed easily by washing, suggesting high fouling release and easy-cleaning capacity. This study provides useful insight in the combined “fouling resistance” and “fouling release�

Cross-Linked Poly(vinylidene fluoride-co-hexafluoropropene (PVDF-co-HFP Gel Polymer Electrolyte for Flexible Li-Ion Battery Integrated with Organic Light Emitting Diode (OLED

Directory of Open Access Journals (Sweden)

Ilhwan Kim

2018-04-01

Full Text Available Here, we fabricate poly(vinylidene fluoride-co-hexafluoropropene (PVDF-co-HFP by electrospinning for a gel polymer electrolyte (GPE for use in flexible Li-ion batteries (LIBs. As a solvent, we use N-methyl-2-pyrrolidone (NMP, which helps produce the cross-linked morphology of PVDF-co-HFP separator, owing to its low volatility. The cross-linked PVDF-co-HFP separator shows an uptake rate higher than that of a commercialized polypropylene (PP separator. Moreover, the PVDF-co-HFP separator shows an ionic conductivity of 2.3 × 10−3 S/cm at room temperature, comparable with previously reported values. An LIB full-cell assembled with the PVDF-co-HFP-based GPE shows capacities higher than its counterpart with the commercialized PP separator, confirming that the cross-linked PVDF-co-HFP separator provides highly efficient ionic conducting pathways. In addition, we integrate a flexible LIB cell using the PVDF-co-HFP GPE with a flexible organic light emitting diode (OLED, demonstrating a fully flexible unit of LIB and OLED.

Selective adsorption of Pb (II) ions by amylopectin-g-poly (acrylamide-co-acrylic acid): A bio-degradable graft copolymer.

Science.gov (United States)

Sasmal, Dinabandhu; Maity, Jayanta; Kolya, Haradhan; Tripathy, Tridib

2017-04-01

Amylopectin-g-poly (acrylamide-co-acrylic acid) [AP-g-poly (AM-co-AA)] was synthesised in water medium by using potassium perdisulphate as an initiator. The graft copolymer was characterized by molecular weight determination by size exclusion chromatography (SEC), fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) spectroscopy, scanning electron microscope (SEM) studies, thermal analysis, measurement of neutralisation equivalent and biodegradation studies. The graft copolymer was used for Pb (II) ion removal from aqueous solution. The Pb (II) ion removal capacity of the graft copolymer was also compared with another laboratory developed graft copolymer Amylopectin-g-poly (acrylamide) (AP-g-PAM). Both the graft copolymers were also used for the competitive metal ions removal with Pb (II)/Cd (II), Pb (II)/Zn (II), Pb (II)/Ni (II), Pb (II)/Cu (II) pairs separately under similar conditions. AP-g-poly (AM-co-AA) showed better Pb (II) ion adsorbing power over AP-g-PAM and also much selective towards Pb (II) ions. The adsorption follows a second order rate equation and Langmuir isotherm model. Copyright © 2017 Elsevier B.V. All rights reserved.

Conductive materials for proton exchange membrane fuel cell bipolar plates made from PVDF, PET and co-continuous PVDF/PET filled with carbon additives

Energy Technology Data Exchange (ETDEWEB)

Nguyen, L.; Mighri, F.; Deyrail, Y. [CREPEC, Center for Applied Research on Polymers and Composites, QC (Canada); Department of Chemical Engineering, Laval University, QC (Canada); Elkoun, S. [CREPEC, Center for Applied Research on Polymers and Composites, QC (Canada); Department of Mechanical Engineering, Sherbrooke University, QC (Canada)

2010-12-15

The aim of this work was to develop and characterise electrically conductive materials for proton exchange membrane fuel cells and bipolar plates (BPPs). These BPPs were made from highly conductive blends of polyethylene terephthalate (PET) and polyvinylidene fluoride (PVDF), as matrix phase. The conductive materials were developed from carefully formulated blends composed of conductive carbon black (CB) powder and, in some cases, graphite synthetic flakes mixed with pure PET, PVDF or with PVDF/PET systems. They were first developed by twin-screw extrusion process then compression-molded to give BPP final shape. As the developed blends have to meet properties suitable for BPP applications, they were characterised for their rheological properties, electrical through-plane resistivity (the inverse of conductivity), oxygen permeability, flexural and impact properties. Results showed that lower resistivity was obtained with PVDF/CB blends due to the higher interfacial energy between the PVDF matrix and CB and also the higher density and crystallinity of PVDF, compared to those of PET. It was also observed that the lowest resistivity values were obtained with mixing PVDF and PET at controlled compositions to ensure PVDF/PET co-continuous morphology. Also, slow cooling rates helped to attain the lowest values of through-plane resistivity for all studied blends. This behaviour was related to the higher crystallinity obtained with low cooling rates leading to smaller amorphous regions in which carbon particles are much more concentrated. (Copyright copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Lysozyme-immobilized electrospun PAMA/PVA and PSSA-MA/PVA ion-exchange nanofiber for wound healing.

Science.gov (United States)

Tonglairoum, Prasopchai; Ngawhirunpat, Tanasait; Rojanarata, Theerasak; Opanasopit, Praneet

2014-08-27

Abstract This research was aimed to develop the lysozyme immobilized ion-exchange nanofiber mats for wound healing. To promote the healing process, the PSSA-MA/PVA and PAMA ion-exchange nanofiber mats were fabricated to mimic the extracellular matrix structure using electrospinning process followed by thermally crosslinked. Lysozyme was immobilized on the ion-exchane nanofibers by an adsorption method. The ion-exchange nanofibers were investigated using SEM, FTIR and XRPD. Moreover, the lysozyme-immobilized ion-exchange nanofibers were further investigated for lysozyme content and activity, lysozyme release and wound healing activity. The fiber diameters of the mats were in the nanometer range. Lysozyme was gradually absorbed into the PSSA-MA/PVA nanofiber with higher extend than that is absorbed on the PAMA/PVA nanofiber and exhibited higher activity than lysozyme-immobilized PAMA/PVA nanofiber. The total contents of lysozyme on the PSSA-MA/PVA and PAMA/PVA nanofiber were 648 and 166 µg/g, respectively. FTIR and lysozyme activity results confirmed the presence of lysozyme on the nanofiber mats. The lysozyme was released from the PSSA-MA/PVA and PAMA/PVA nanofiber in the same manner. The lysozyme-immobilized PSSA-MA/PVA nanofiber mats and lysozyme-immobilized PAMA/PVA nanofiber mats exhibited significantly faster healing rate than gauze and similar to the commercial antibacterial gauze dressing. These results suggest that these nanofiber mats could provide the promising candidate for wound healing application.

PVDF-based copolymers, terpolymers and their multi-component material systems for capacitor applications

Science.gov (United States)

Chu, Baojin

at 1 kHz at room temperature), were further investigated for dielectric materials of high energy density. Due to the lower dielectric constant, the early polarization saturation was avoided and these polymers showed a very high breakdown field and energy density. For the P(VDF-CTFE) copolymer with 15 wt% CTFE, an energy density of higher than 24 J/cm 3 at an electric field higher than 650 MV/m could be obtained. Based on thermal and microstructure studies, the high energy density was found to be caused by the structural modification of PVDF by bulky CTFE or HFP, which also act as defects, similar to the terpolymers. The discharge behavior of the copolymers mainly relies on the load resistors, suggesting that the copolymers have lower equivalent series resistance. Multi-component material system based on current available materials was found to be a useful strategy to tailor and improve the performance of dielectric materials. Nanocomposites composed of the P(VDF-TrFE-CFE) terpolymers and ZrO2 or TiO2 nanoparticles were found to greatly enhance the polarization response and energy density of terpolymers (from 9 J/cm3 to 10.5 J/cm3). Based on comprehensive thermal, dielectric and microstructure studies, the enhancement was believed to be related to the large amount of interfaces in the nanocomposites. In the interfaces, the chain mobility is increased and the energy barrier between the polar and nonpolar phases is reduced, resulting in higher polarization response and energy density at a reduced electric field. The P(VDF-TrFE-CFE) terpolymer/P(VDF-CTFE) copolymer and the P(VDFTrFE-CFE) terpolymer/PMMA blends were also studied. It was found that the P(VDFTrFE-CFE) terpolymers could not be completely miscible with the P(VDF-CTFE) copolymer. In the P(VDF-TrFE-CFE) terpolymer/P(VDF-CTFE) copolymer blends, with a small amount of the copolymer (5 and 10 wt%) in the terpolymer, enhancement of the polarization response similar to that observed in the terpolymer/ZrO 2

Zwitterionic sulfobetaine-grafted poly(vinylidene fluoride) membrane surface with stably anti-protein-fouling performance via a two-step surface polymerization

Energy Technology Data Exchange (ETDEWEB)

Li Qian; Bi Qiuyan; Zhou Bo [Membrane Technology and Engineering Research Center, Department of Chemical Engineering, Tsinghua University, Beijing 100084 (China); Wang Xiaolin, E-mail: xl-wang@tsinghua.edu.cn [Membrane Technology and Engineering Research Center, Department of Chemical Engineering, Tsinghua University, Beijing 100084 (China)

2012-03-01

A zwitterionic polymer, poly(3-(methacryloylamino) propyl-dimethyl-(3-sulfopropyl) ammonium hydroxide) (poly(MPDSAH)) was successfully grafted in high density from the surface of poly(vinylidene fluoride) (PVDF) hollow fiber membrane via a two-step polymerization. Poly(2-hydroxyethyl methacrylate) (poly(HEMA)) chains were firstly grafted from outside surface of PVDF membrane through atom transfer radical polymerization (ATRP) to provide the initiation sites for subsequent cerium (Ce (IV))-induced graft copolymerization of polyMPDSAH in the presence of N,N Prime -ethylene bisacrylamide (EBAA) as a cross-linking agent. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) confirmed that the EBAA could stimulate zwitterionic polymers grafting onto the membrane surface. The dense poly(MPDSAH) layers on the PVDF membrane surface were revealed by the scanning electron microscope (SEM). The mechanical property of PVDF membrane was improved by the zwitterionic surface layers. The gravimetry results indicated the grafting amount increased to 520 {mu}g/cm{sup 2} for a copolymerization time of more than 3 h. Static and dynamic water contact angle measurements showed that the surface hydrophilicity of the PVDF membranes was significantly enhanced. As the grafting amount reached 513 {mu}g cm{sup -2}, the value of contact angle dropped to 22.1 Degree-Sign and the amount of protein adsorption decreased to zero. The cyclic experiments for BSA solution filtration demonstrated that the extent of protein fouling was significantly reduced and most of the fouling was reversible. The grafted polymer layer on the PVDF membrane showed a good stability during the membrane cleaning process. The experimental results concluded a good prospect in obtaining the sulfobetaine-modified PVDF membranes with high mechanical strength, good anti-protein-fouling performance, and long-term stability via the two-step polymerization.

Zwitterionic sulfobetaine-grafted poly(vinylidene fluoride) membrane surface with stably anti-protein-fouling performance via a two-step surface polymerization

International Nuclear Information System (INIS)

Li Qian; Bi Qiuyan; Zhou Bo; Wang Xiaolin

2012-01-01

A zwitterionic polymer, poly(3-(methacryloylamino) propyl-dimethyl-(3-sulfopropyl) ammonium hydroxide) (poly(MPDSAH)) was successfully grafted in high density from the surface of poly(vinylidene fluoride) (PVDF) hollow fiber membrane via a two-step polymerization. Poly(2-hydroxyethyl methacrylate) (poly(HEMA)) chains were firstly grafted from outside surface of PVDF membrane through atom transfer radical polymerization (ATRP) to provide the initiation sites for subsequent cerium (Ce (IV))-induced graft copolymerization of polyMPDSAH in the presence of N,N′-ethylene bisacrylamide (EBAA) as a cross-linking agent. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) confirmed that the EBAA could stimulate zwitterionic polymers grafting onto the membrane surface. The dense poly(MPDSAH) layers on the PVDF membrane surface were revealed by the scanning electron microscope (SEM). The mechanical property of PVDF membrane was improved by the zwitterionic surface layers. The gravimetry results indicated the grafting amount increased to 520 μg/cm 2 for a copolymerization time of more than 3 h. Static and dynamic water contact angle measurements showed that the surface hydrophilicity of the PVDF membranes was significantly enhanced. As the grafting amount reached 513 μg cm -2 , the value of contact angle dropped to 22.1° and the amount of protein adsorption decreased to zero. The cyclic experiments for BSA solution filtration demonstrated that the extent of protein fouling was significantly reduced and most of the fouling was reversible. The grafted polymer layer on the PVDF membrane showed a good stability during the membrane cleaning process. The experimental results concluded a good prospect in obtaining the sulfobetaine-modified PVDF membranes with high mechanical strength, good anti-protein-fouling performance, and long-term stability via the two-step polymerization.

Determining the degree of grafting for poly (vinylidene fluoride) graft-copolymers using fluorine elemental analysis

International Nuclear Information System (INIS)

Yu Yang; Zhang Bowu; Yang Xuanxuan; Deng Bo; Li Linfan; Yu Ming; Li Jingye

2011-01-01

Acrylic acid (AAc) and styrene (St) were grafted onto poly (vinylidene fluoride) (PVDF) powder or membrane samples by pre-irradiation graft copolymerization. The grafted chains were proved by FT-IR spectroscopy analysis. The degree of grafting (DG) of the grafted PVDF was determined by fluorine elemental analysis (FEA) method, and was compared with the DGs determined by weighing method, acid-base back titration method and quantitative FT-IR method. The results show that the FEA method is accurate, convenient and universal, especially for the grafted polymer powders. (authors)

Preparation and application of PVDF-HFP composite polymer electrolytes in LiNi0.5Co0.2Mn0.3O2 lithium-polymer batteries

International Nuclear Information System (INIS)

Yang, Chun-Chen; Lian, Zuo-Yu; Lin, S.J.; Shih, Jeng-Ywan; Chen, Wei-Houng

2014-01-01

Graphical abstract: - Highlights: • PVDF-HFP/SBA15 membrane and NCM cathode material were prepared for Li ion battery. • SBA15 fillers can trap more liquid electrolytes to enhance the ionic conductivity. • Modified fillers with functional groups play a key role in reducing impedance. • LiNi 0.5 Co 0.2 Mn 0.3 O 2 polymer battery showed excellent electrochemical performance. - Abstract: This study reports the preparation of a composite polymer electrolyte for application in LiNi 0.5 Co 0.2 Mn 0.3 O 2 lithium-polymer batteries. Poly(vinylidiene fluoride-hexafluoropropylene) (denoted as PVDF-HFP) was used as the polymer host and mesoporous modified-silica fillers (denoted as m-SBA15) used as the solid plasticizer were added into the polymer matrix. The characteristic properties of the composite polymer membranes were examined using Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), and an AC impedance method. The discharge capacities of LiNi 0.5 Co 0.2 Mn 0.3 O 2 polymer batteries with a PE separator, pure PVDF-HFP polymer membrane, or a PVDF-HFP/10 wt.%m-SBA15 composite at 0.1 C were determined to be 155.5, 159.5, and 198.6 mAh g −1 , respectively. The LiNi 0.5 Co 0.2 Mn 0.3 O 2 polymer battery containing the PVDF-HFP/10 wt.%m-SBA15 composite achieved discharge capacities of 194, 170, 161, 150, 129, 115, and 87 mAh g −1 at 0.1, 0.2, 0.5, 1, 3, 5, and 10 C, respectively. The lithium-polymer battery demonstrated a high coulomb efficiency of ca. 99%. The PVDF-HFP/m-SBA15 composite membrane is a strong candidate for application in LiNi 0.5 Co 0.2 Mn 0.3 O 2 lithium-polymer batteries

Development of Less Water-Dependent Radiation Grafted Proton Exchange Membranes for Fuel Cells

Energy Technology Data Exchange (ETDEWEB)

Nasef, M M; Ahmad, A; Saidi, H; Dahlan, K Z.M. [Institute of Hydrogen Economy, Energy Research Alliance (ERA), International Campus, Univeristi Teknologi Malaysia, Jalan Semarak, Kuala Lumpur (Malaysia); Radiation Processing Division, Malaysian Nuclear Agency, Bangi, Kajang (Malaysia)

2012-09-15

The aim of these studies was the development of proton exchange membranes for polymer electrolyte membrane (PEM) fuel cell operated above 100{sup o}C, in order to obtain less water dependent, high quality and cheap electrolyte membrane. Sulfonic acid membranes were prepared by radiation induced grafting (RIG) of sodium styrene sulfonate (SSS) onto electron beam (EB) irradiated poly(vinylidene fluoride) (PVDF) films in a single step reaction for the first time using synergetic effect of acid addition to grafting mixture under various grafting conditions. The fuel cell related properties of the membranes were evaluated and the in situ performance was tested in a single H{sub 2}/O{sub 2} fuel cell under dynamic conditions and compared with a similar sulfonated polystyrene PVDF membrane obtained by two-step conventional RIG method i.e. grafting of styrene and subsequent sulfonation. The newly obtained membrane (degree of grafting, G% = 53) showed an improved performance and higher stability together with a cost reduction mainly as a result of elimination of sulfonation reaction. Acid-base composite membranes were also studied. EB pre-irradiated poly(ethylene-co-tetrafluoroethylene) (ETFE) films were grafted with N-vinyl pyridine (NVP). The effects of monomer concentration, dose, reaction time, film thickness, temperature and film storage time on G% were investigated. The membranes were subsequently doped with phosphoric acid under controlled condition. The proton conductivity of these membranes was investigated under low water conditions in correlation with the variation in G% and temperature (30-130{sup o}C). The performance of 34 and 49% grafted and doped membranes was tested in a single fuel cell at 130{sup o}C under dynamic conditions with 146 and 127 mW/cm{sup 2} power densities. The polarization, power density characteristics and the initial stability of the membrane showed a promising electrolyte candidate for fuel cell operation above 100 deg. C. (author)

Tethering of hyperbranched polyols using PEI as a building block to synthesize antifouling PVDF membranes

Science.gov (United States)

Wang, Xushan; Wang, Zihong; Wang, Zhe; Cao, Yu; Meng, Jianqiang

2017-10-01

Antifouling PVDF membranes were prepared by grafting hyperbranched polyols on the membrane surface via a three-step modification method. The membrane was first prepared by alkaline treatment to introduce alkenyl groups, then chemically immobilizing hyperbranched poly(ethyleneimine) (HPEI) on membrane surface through Michael reaction followed by ring opening reaction of the glycidol with amine groups. Chemical compositions, surface morphology and physicochemical properties of the original and modified membranes were characterized via attenuated total refection-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), water contact angle (WCA) and zeta potential measurements. The antifouling property of the modified membrane was assessed by the static bovine serum albumin (BSA) and lysozyme (LZM) adsorption as well as cross-flow filtration of BSA aqueous solution. The results explicate that surface modification using hyperbranched polymers can alter membrane chemistry and morphology significantly. In contrast to the original PVDF membrane, the modified membrane shows superhydrophilic property and relatively high capability to resist nonspecific protein adsorption. Three HPEIs were used for modification and the obtained PVDFA-g-PG60,000 membrane has a static BSA protein adsorption of 45 μg/cm2 and shows the highest protein resistance. However, the PVDF-g-PG membrane is positively charged due to the unreacted amine groups. As a result, the PVDF-g-PG membranes also show high flux decline during the filtration of BSA aqueous solution due to the electrostatic interaction. In spite of that, the PVDF-g-PG membranes still maintain high flux recovery ratio and good washing properties.

TEMPO addition into pre-irradiated fluoropolymers and living-radical graft polymerization of styrene for preparation of polymer electrolyte membranes

Energy Technology Data Exchange (ETDEWEB)

Sawada, Shin-ichi, E-mail: sawada.shinnichi@jaea.go.j [Conducting Polymer Materials Research Group, Quantum Beam Science Directorate, Japan Atomic Energy Agency (JAEA), 1233 Watanuki, Takasaki, Gunma 370-1292 (Japan); Department of Nuclear Engineering and Management, Graduate School of Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Suzuki, Akihiro; Terai, Takayuki [Department of Nuclear Engineering and Management, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Maekawa, Yasunari, E-mail: maekawa.yasunari@jaea.go.j [Conducting Polymer Materials Research Group, Quantum Beam Science Directorate, Japan Atomic Energy Agency (JAEA), 1233 Watanuki, Takasaki, Gunma 370-1292 (Japan)

2010-04-15

We prepared proton exchange membranes (PEMs) by 2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO)-mediated living-radical graft polymerization (LRGP) of styrene into fluoropolymer films and subsequent sulfonation. Poly(vinylidene fluoride) (PVDF) and poly(ethylene-co-tetrafluoroethylene) (ETFE) films were first irradiated and then treated with TEMPO solutions in various solvents. TEMPO addition was confirmed by the test of styrene grafting into TEMPO-treated films at 60 deg. C, at which the LRGP never proceeds. This test enabled us to differentiate the LRGP from the conventional graft polymerization. In order to gain a deep insight about TEMPO-addition reaction, the TEMPO-penetration behavior into the base polymer films was examined by a permeation experiment and computer simulation. Xylene and dioxane were appropriate solvents for the complete introduction of TEMPO into PVDF and ETFE films, respectively. Then, the LRGP of styrene was performed based on the fully TEMPO-capped films at 125 deg. C with various solvents. By using an alcoholic solvent, the degree of grafting was enhanced and it reached a maximum of 38%. This grafted film was sulfonated to prepare a PEM showing an ion exchange capacity of 2.2 meq/g and proton conductivity of 1.6x10{sup -1} S/cm.

Superhydrophobic PVDF and PVDF-HFP nanofibrous mats with antibacterial and anti-biofouling properties

Energy Technology Data Exchange (ETDEWEB)

Spasova, M.; Manolova, N. [Laboratory of Bioactive Polymers, Institute of Polymers, Bulgarian Academy of Sciences, Acad. G. Bonchev St, bl. 103A, BG-1113 Sofia (Bulgaria); Markova, N. [Institute of Microbiology, Bulgarian Academy of Sciences, Acad. G. Bonchev St, bl. 26, BG-1113 Sofia (Bulgaria); Rashkov, I., E-mail: rashkov@polymer.bas.bg [Laboratory of Bioactive Polymers, Institute of Polymers, Bulgarian Academy of Sciences, Acad. G. Bonchev St, bl. 103A, BG-1113 Sofia (Bulgaria)

2016-02-15

Graphical abstract: - Highlights: • New PVDF and PVDF-HFP nanofibers decorated with ZnO nanoparticles and a model drug. • The nanofibrous materials were fabricated by one-pot electrospinning. • The obtained materials are superhybrophobic and possess antibacterial properties. - Abstract: Superhydrophobic nanofibrous materials of poly(vinylidene fluoride) (PVDF) and poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) were prepared by one-pot electrospinning technique. The mats were decorated with ZnO nanoparticles with silanized surface and a model drug – 5-chloro-8-hydroxyquinolinol (5Cl8HQ). The obtained hybrid nanofibrous materials were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), contact angle measurements, mechanical and microbiological tests. The results showed that the incorporation of ZnO nanoparticles into PVDF and PVDF-HFP nanofibers increased the hydrophobicity (contact angle 152°), improved the thermal stability and imparted to the nanofibrous materials anti-adhesive and antimicrobial properties. The mats containing the model drug possessed antibacterial activity against Escherichia coli and Staphylococcus aureus. The results suggested that the obtained hybrid mats could find potential biomedical applications requiring antibacterial and anti-biofouling properties.

PMMA-g-OEtOx Graft Copolymers: Influence of Grafting Degree and Side Chain Length on the Conformation in Aqueous Solution

Directory of Open Access Journals (Sweden)

Irina Muljajew

2018-03-01

Full Text Available Depending on the degree of grafting (DG and the side chain degree of polymerization (DP, graft copolymers may feature properties similar to statistical copolymers or to block copolymers. This issue is approached by studying aqueous solutions of PMMA-g-OEtOx graft copolymers comprising a hydrophobic poly(methyl methacrylate (PMMA backbone and hydrophilic oligo(2-ethyl-2-oxazoline (OEtOx side chains. The graft copolymers were synthesized via reversible addition-fragmentation chain transfer (RAFT copolymerization of methyl methacrylate (MMA and OEtOx-methacrylate macromonomers of varying DP. All aqueous solutions of PMMA-g-OEtOx (9% ≤ DG ≤ 34%; 5 ≤ side chain DP ≤ 24 revealed lower critical solution temperature behavior. The graft copolymer architecture significantly influenced the aggregation behavior, the conformation in aqueous solution and the coil to globule transition, as verified by means of turbidimetry, dynamic light scattering, nuclear magnetic resonance spectroscopy, and analytical ultracentrifugation. The aggregation behavior of graft copolymers with a side chain DP of 5 was significantly affected by small variations of the DG, occasionally forming mesoglobules above the cloud point temperature (Tcp, which was around human body temperature. On the other hand, PMMA-g-OEtOx with elongated side chains assembled into well-defined structures below the Tcp (apparent aggregation number (Nagg = 10 that were able to solubilize Disperse Orange 3. The thermoresponsive behavior of aqueous solutions thus resembled that of micelles comprising a poly(2-ethyl-2-oxazoline (PEtOx shell (Tcp > 60 °C.

Modeling and optimization aspects of radiation induced grafting of 4-vinylpyridene onto partially fluorinated films

International Nuclear Information System (INIS)

Nasef, Mohamed Mahmoud; Ahmad Ali, Amgad; Saidi, Hamdani; Ahmad, Arshad

2014-01-01

Modeling and optimization aspects of radiation induced grafting (RIG) of 4-vinylpyridine (4-VP) onto partially fluorinated polymers such as poly(ethylene-co-tetrafluoroethene) (ETFE) and poly(vinylidene fluoride) (PVDF) films were comparatively investigated using response surface method (RSM). The effects of independent parameters: absorbed dose, monomer concentration, grafting time and reaction temperature on the response, grafting yield (GY) were correlated through two quadratic models. The results of this work confirm that RSM is a reliable tool not only for optimization of the reaction parameters and prediction of GY in RIG processes, but also for the reduction of the number of the experiments, monomer consumption and absorbed dose leading to an improvement of the overall reaction cost. - Highlights: • Comparative study of radiation induced grafting of 4-VP onto PVDF and ETFE films. • Optimization of reaction parameters for both grafting systems was made using RSM. • Single factor design for both grafting systems was used as a reference. • Two quadratic regression models were developed for prediction of grafting yield. • RSM is an effective tool for handling grafting reactions under different conditions

Radiolytical Preparation of a Poly(Vinylbenzyl Sulfonic Acid)-Grafted FEP Membrane and Characterization as Polymer Electrolytes for Direct Methanol Fuel Cells

Energy Technology Data Exchange (ETDEWEB)

Nho, Y -C; Shin, J; Sohn, J -Y; Fei, G [Radiation Research Division for Industry and Environment, Korea Atomic Energy Research Institute, 1266 Sinjeong-dong, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of)

2012-09-15

In this study, a novel polymer electrolyte membrane, poly(vinylbenzyl sulfonic acid)-grafted poly(tetrafluoroethylene-co-hexafluoropropylene) (FEP-g-PVBSA), has been successfully prepared by simultaneous irradiation grafting of vinylbenzyl chloride(VBC) monomer onto a FEP film and taking subsequent chemical modification steps to modify the benzyl chloride moiety to the benzyl sulfonic acid moiety. The chemical reactions for the sulfonation were carried out via the formation of thiouronium salt with thiourea, base-catalyzed hydrolysis for the formation of thiol, and oxidation with hydrogen peroxide. Each chemical conversion process was confirmed by FTIR, elemental analysis, and SEM-EDX. A chemical stability study performed with Fenton's reagent (3% H{sub 2}O{sub 2} solution containing 4 ppm of Fe{sup 2+}) at 70 deg. C revealed that FEP-g-PVBSA has a higher chemical stability than the poly(styrene sulfonic acid)-grafted membranes (FEP-g-PSSA). An EDX analysis was also used to observe the cross-sectional distribution behaviors of the hydrophilic sulfonic acid groups and hydrophobic fluorine groups. The characteristics of an ion-exchange capacity (IEC), water and methanol uptake, methanol permeability, and proton conductivity as a function of the degree of grafting were also studied. The IECs and water uptakes of membranes with different degrees of grafting (36-102%) were measured to be in the range of 0.8-1.62 meq/g, and 10-30%, respectively. When the degree of grafting reached 60% the proton conductivity was higher than that of a Nafion (registered) 212 membrane (6.1E-02 S/cm). The methanol permeability and uptake of the FEP-g-PVBSA membrane was significantly lower than that of the Nafion (registered) 212 membrane, and even the degree of grafting reached 102%. (author)

Synthesis of hydrophilic carbon nanotubes by grafting poly(methyl methacrylate) via click reaction and its effect on poly(vinylidene fluoride)-carbon nanotube composite membrane properties1

Science.gov (United States)

Ma, Wenzhong; Zhao, Yuchen; Li, Yuxue; Zhang, Peng; Cao, Zheng; Yang, Haicun; Liu, Chunlin; Tao, Guoliang; Gong, Fanghong; Matsuyama, Hideto

2018-03-01

Surface modification of azide-decorated multiwalled carbon nanotubes (MWCNTs) with well-defined alkyne-terminated poly(methyl methacrylate) (PMMA) chains was accomplished via the combination of reversible addition fragmentation chain transfer (RAFT) and "click" chemistry. Successful attachment of PMMA onto MWCNT was confirmed by Fourier transform infrared spectroscopy, thermogravimetric analysis (TGA), gel permeation chromatography, Raman spectroscopy, and transmission electron microscopy. The highest grafting percentage (GP) of the PMMA chains (GP = 23.3%) was calculated using TGA. The effect of the PMMA-grafted-MWCNTs (MWCNTs-g-PMMA) content on the performance of the poly(vinylidene fluoride) (PVDF)-MWCNTs-g-PMMA composite membrane was studied. The MWCNTs-g-PMMA was found to be well dispersed in the PVDF composite membrane matrix because of the excellent compatibility between the PMMA and PVDF chains. The composite membranes showed improved porosity, hydrophilicity, water flux, β-PVDF content, and mechanical properties at an optimal amount of 2 wt% MWCNTs-g-PMMA incorporated in the PVDF membrane matrix. In contrast, the hydroxyl functionalized MWCNTs (MWCNTs-OH) showed limited enhancement in the water flux and mechanical strength, which is mainly due to the poor dispersion of MWCNT because of the weak interaction between the MWCNT and PVDF chains. This study reveals the excellent prospect of the MWCNT-based ultrafiltration membrane with enhanced properties in water treatment applications.

Controlled Grafting of Poly(methyl methacrylate) Brushes on Poly(vinylidene fluoride) Powders by Surface-initiated Atom Transfer Radical Polymerization

Institute of Scientific and Technical Information of China (English)

TANG Zhaoqi; LI Wei; LIU Lanqin; HUANG Lei; ZHOU Jin; YU Haiyin

2009-01-01

Controlled grafting of well-defined polymer brushes of methyl methacrylate (MMA) on the poly(vinylidene fluoride) (PVDF) powders was carded out by the surface-initiated atom transfer radical polymerization (ATRP). The ATRP initiator was anchored on the PVDF surface by alkaline treatment, followed by UV-induced bromination; then methyl methacrylate (MMA) was grafted onto the brominated PVDF by the ATRP technique. The chemical composition changes of PVDF were characterized by Fourier transform-infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). FT-IR and XPS results clearly indicated the successful graft of poly(methyl methacrylate) onto the PVDF surface.

The Impact of the School-Based Psychosocial Structured Activities (PSSA) Program on Conflict-Affected Children in Northern Uganda

Science.gov (United States)

Ager, Alastair; Akesson, Bree; Stark, Lindsay; Flouri, Eirini; Okot, Braxton; McCollister, Faith; Boothby, Neil

2011-01-01

Background: Children in northern Uganda have undergone significant psychosocial stress during the region's lengthy conflict. A Psychosocial Structured Activities (PSSA) program was implemented in 21 schools identified as amongst those most severely affected by conflict-induced displacement across Gulu and Amuru Districts. The PSSA intervention…

Composite vascular grafts with high cell infiltration by co-electrospinning

International Nuclear Information System (INIS)

Tan, Zhikai; Wang, Hongjie; Gao, Xiangkai; Liu, Tong; Tan, Yongjun

2016-01-01

There is an increasing demand for functional small-diameter vascular grafts (diameter < 6 mm) to be used in clinical arterial replacement. An ideal vascular graft should have appropriate biomechanical properties and be biocompatible. Electrospinning has become a popular polymer processing technique for vascular tissue engineering, but the grafts fabricated by electrospinning often have relatively small pores and low porosity, which limit cell infiltration into scaffolds and hinder the regeneration and remodeling of grafts. In the present study, we aimed to develop an efficient method to prepare electrospun composite vascular grafts comprising natural and synthetic materials. We fabricated grafts made of polycaprolactone, gelatin, and polyvinyl alcohol (PVA) by co-electrospinning, and the scaffolds were further functionalized by immobilizing heparin on them. The PVA fibers degraded rapidly in vivo and generated electrospun scaffolds with high porosity, which significantly enhanced cell proliferation and infiltration. The mechanical properties of the grafts are suitable for use in artery replacement. Heparin functionalization of the grafts yielded a good antithrombogenic effect, which was demonstrated in platelet adhesion tests. Moreover, in vitro and in vivo results demonstrated that the heparin release from the grafts enhanced the growth of endothelial cells, which is important for the endothelium of implanted grafts. The results of this study indicate that our method is effective and controllable for the fabrication of vascular grafts that meet the clinical requirements for blood vessel transplantation. - Highlights: • This study indicate an effective method for the fabrication of vascular grafts that meet the clinical requirements. • Co-electrospinning were used to fabricate grafts made of polycaprolactone (PCL), gelatin (GT), and polyvinyl alcohol (PVA). • PVA was used to create large pores within the hybrid scaffolds, thereby enhancing cell infiltration

Composite vascular grafts with high cell infiltration by co-electrospinning

Energy Technology Data Exchange (ETDEWEB)

Tan, Zhikai, E-mail: tanzk@hnu.edu.cn; Wang, Hongjie; Gao, Xiangkai; Liu, Tong; Tan, Yongjun

2016-10-01

There is an increasing demand for functional small-diameter vascular grafts (diameter < 6 mm) to be used in clinical arterial replacement. An ideal vascular graft should have appropriate biomechanical properties and be biocompatible. Electrospinning has become a popular polymer processing technique for vascular tissue engineering, but the grafts fabricated by electrospinning often have relatively small pores and low porosity, which limit cell infiltration into scaffolds and hinder the regeneration and remodeling of grafts. In the present study, we aimed to develop an efficient method to prepare electrospun composite vascular grafts comprising natural and synthetic materials. We fabricated grafts made of polycaprolactone, gelatin, and polyvinyl alcohol (PVA) by co-electrospinning, and the scaffolds were further functionalized by immobilizing heparin on them. The PVA fibers degraded rapidly in vivo and generated electrospun scaffolds with high porosity, which significantly enhanced cell proliferation and infiltration. The mechanical properties of the grafts are suitable for use in artery replacement. Heparin functionalization of the grafts yielded a good antithrombogenic effect, which was demonstrated in platelet adhesion tests. Moreover, in vitro and in vivo results demonstrated that the heparin release from the grafts enhanced the growth of endothelial cells, which is important for the endothelium of implanted grafts. The results of this study indicate that our method is effective and controllable for the fabrication of vascular grafts that meet the clinical requirements for blood vessel transplantation. - Highlights: • This study indicate an effective method for the fabrication of vascular grafts that meet the clinical requirements. • Co-electrospinning were used to fabricate grafts made of polycaprolactone (PCL), gelatin (GT), and polyvinyl alcohol (PVA). • PVA was used to create large pores within the hybrid scaffolds, thereby enhancing cell infiltration

Surface Modifications of Polymers Induced by Heavy Ions Grafting

Energy Technology Data Exchange (ETDEWEB)

Mazzei, R O; Lombardo, J; Camporotondi, D; Tadey, D; Bermudez, G G [National Atomic Energy Commission, Ezeiza Atomic Centre, Ezeiza (Argentina)

2012-09-15

Polymer surfaces are modified by the application of swift heavy ions etching and grafting procedures. The residual active sites produced by heavy ion beams, remaining after the etching process, were used to start the grafting process. In order to produce tracks on foils of poly(vinylidene fluoride) (PVDF) they were irradiated with {sup 208}Pb of 25.62 MeV/n or with 115 MeV Cl ions. Moreover, foils of polypropylene (PP) were irradiated with {sup 208}Pb of 25.62 MeV/n. Then, they were etched and grafted with N-isopropylacrylamide (NIPAAm) monomers or with acrylic acid (AAc) monomers, respectively. The replica method allowed the observation of the shape of the grafted tracks using transmission electron microscopy (TEM). In addition NIPAAm grafted foils were analyzed using Fourier transform infrared spectroscopy (FTIR). The sulfonation procedure (methodology previously described for perfluorated polymers) was applied on grafted PVDF. A new method is described to produce a thin layer of poly-acrylic-acid (membranes) that grows on the surface of PVDF foils implanted by an Ar{sup +} beam with energies between 30-150 keV. Different combinations of monomers in water solutions were used such as: acrylic acid (AAc); acrylic acid-glycidyl methacrylate (AAc-GMA); acrylic acid-styrene (AAc-S); acrylic acid-N-isopropyl acrylamide (AAc-NIPAAm) and acrylic acid-N-isopropyl acrylamide - glycidyl methacrylate (AAc-NIPAAm-GMA). The experimental results show that for particular values of: ion fluence and energy, AAc concentration, sulphuric acid and PVDF polymorphous (alpha or beta) a huge percentage of grafting was obtained. At certain point of the grafting process the development of the PolyAAc-Xmonomer produce a detachment from the irradiated substrate and continue its grafting outside it. This method produces a membrane that is an increased replica of the original implanted surface. Finally, PVDF films implanted by an Ar{sup +} beam with energies about 100 keV and a fluence of 10

Synthesis, Characterization, and Aqueous Lubricating Properties of Amphiphilic Graft Copolymers Comprising 2-Methoxyethyl Acrylate

DEFF Research Database (Denmark)

Javakhishvili, Irakli; Røn, Troels; Jankova Atanasova, Katja

2014-01-01

Amphiphilic anionic and cationic graft copolymers possessing poly(2-hydroxyethyl methacrylate) (PHEMA) backbone and poly(methacrylic acid), poly(2-methoxyethyl acrylate-co-methacrylic acid), and poly(2-methoxyethyl acrylate-co-2-(dimethylamino)ethyl methacrylate) grafts are constructed by merging...... of the corresponding monomers followed by deblocking reaction leads to well-defined amphiphiles with narrow molecular weight distributions (PDI ≤ 1.29) and varying content of methacrylic acid. The graft copolymers showed effective surface adsorption and lubrication for self-mated poly(dimethylsiloxane) (PDMS) contacts...

Development of robust fluorinated TiO2/PVDF composite hollow fiber membrane for CO2 capture in gas-liquid membrane contactor

Science.gov (United States)

Lin, Yuqing; Xu, Yilin; Loh, Chun Heng; Wang, Rong

2018-04-01

Gas-liquid membrane contactor (GLMC) is a promising method to attain high efficiency for CO2 capture from flue gas, biogas and natural gas. However, membranes used in GLMC are prone to pore wetting due to insufficient hydrophobicity and low chemical resistance, resulting in significant increase in mass transfer resistance. To mitigate this issue, inorganic-organic fluorinated titania/polyvinylidene fluoride (fTiO2/PVDF) composite hollow fiber (HF) membranes was prepared via facile in-situ vapor induced hydrolyzation method, followed by hydrophobic modification. The proposed composite membranes were expected to couple the superb chemical stability of inorganic and high permeability/low cost of organic materials. The continuous fTiO2 layer deposited on top of PVDF substrate was found to possess a tighter microstructure and better hydrophobicity, which effectively prevented the membrane from wetting and lead to a high CO2 absorption flux (12.7 × 10-3 mol m-2 s-1). In a stability test with 21-day operation of GLMC using 1M monoethanolamine (MEA) as the absorbent, the fTiO2/PVDF membrane remained to be intact with a CO2 absorption flux decline of ∼16%, while the pristine PVDF membrane suffered from a flux decline of ∼80% due to membrane damage. Overall, this work provides an insight into the preparation of high-quality inorganic/organic composite HF membranes for CO2 capture in GLMC application.

Microporous gel electrolytes based on amphiphilic poly(vinylidene fluoride-co-hexafluoropropylene) for lithium batteries

International Nuclear Information System (INIS)

Yu Shicheng; Chen Lie; Chen Yiwang; Tong Yongfen

2012-01-01

Poly(vinylidene fluoride-co-hexafluoropropylene) grafted poly(poly(ethylene glycol) methyl ether methacrylate) (PVDF-HFP-g-PPEGMA) is simply prepared by single-step synthesis directly via atom transfer radical polymerization (ATRP) of poly(ethylene glycol) methyl ether methacrylate (PEGMA) from poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP). Thermal, mechanical, swelling and electrochemical properties, as well as microstructures of the prepared polymer electrolytes, are evaluated and the effects of the various contents and average molecular weights of PEGMA on those properties are also been investigated. By phase inversion technique, the copolymer membranes tend to form well-defined microporous morphology with the increase of content and average molecular weight of PEGMA, due to the competition and cooperation between the hydrophilic PEGMA segments and hydrophobic PVDF-HFP. When these membranes are gelled with 1 M LiCF 3 SO 3 in ethylene carbonate (EC)/propylene carbonate (PC) (1:1, v/v), their saturated electrolyte uptakes (up to 323.5%) and ion conductivities (up to 2.01 × 10 -3 S cm -1 ) are dramatically improved with respect to the pristine PVDF-HFP, ascribing to the strong affinity of the hydrophilic PEGMA segments with the electrolytes. All the polymer electrolytes are electrochemically stable up to 4.7 V versus Li/Li + , and show good mechanical properties. Coin cells based on the polymer electrolytes show stable charge-discharge cycles and deliver discharge capacities to LiFePO 4 is up to 156 mAh g -1 .

Characterization of modified PVDF membrane by gamma irradiation for non-potable water reuse.

Science.gov (United States)

Lim, Seung Joo; Kim, Tak-Hyun; Shin, In Hwan

2015-01-01

Poly(vinylidene fluorine) (PVDF) membranes were grafted by gamma-ray irradiation and were sulfonated by sodium sulfite to modify the surface of the membranes. The characteristics of the modified PVDF membranes were evaluated by the data of Fourier transform infrared (FT-IR), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscope (FE-SEM), the contact angle of the membrane surface and the water permeability. From the results of FT-IR, XPS and FE-SEM, it was shown that the modified membranes were successfully grafted by gamma-ray irradiation and were sulfonated. The content of oxygen and sulfur increased with the monomer concentration, while the content of fluorine sharply decreased. The pore size of the modified membranes decreased after gamma-ray irradiation. The contact angle and the water permeability showed that the hydrophilicity of the modified membranes played a role in determining the membrane performance. The feasibility study of the modified PVDF membranes for using non-potable water reuse were carried out using a laboratory-scale microfiltration system. Grey wastewater was used as the influent in the filtration unit, and permeate quality satisfied non-potable water reuse guidelines in the Republic of Korea.

The Effectiveness of Using STAR Math to Improve PSSA Math Scores

Science.gov (United States)

Holub, Sherry L.

2017-01-01

This is a quantitative study examining whether STAR Math, a student monitoring system, can improve PSSA Math scores. The experimental school used STAR Math during the 2015-2016 school year in grouping students for remediation and intervention. The control school used traditional curriculum measures to group students for remediation and…

Hemocompatibility of poly(vinylidene fluoride) membrane grafted with network-like and brush-like antifouling layer controlled via plasma-induced surface PEGylation.

Science.gov (United States)

Chang, Yung; Shih, Yu-Ju; Ko, Chao-Yin; Jhong, Jheng-Fong; Liu, Ying-Ling; Wei, Ta-Chin

2011-05-03

In this work, the hemocompatibility of PEGylated poly(vinylidene fluoride) (PVDF) microporous membranes with varying grafting coverage and structures via plasma-induced surface PEGylation was studied. Network-like and brush-like PEGylated layers on PVDF membrane surfaces were achieved by low-pressure and atmospheric plasma treatment. The chemical composition, physical morphology, grafting structure, surface hydrophilicity, and hydration capability of prepared membranes were determined to illustrate the correlations between grafting qualities and hemocompatibility of PEGylated PVDF membranes in contact with human blood. Plasma protein adsorption onto different PEGylated PVDF membranes from single-protein solutions and the complex medium of 100% human plasma were measured by enzyme-linked immunosorbent assay (ELISA) with monoclonal antibodies. Hemocompatibility of the PEGylated membranes was evaluated by the antifouling property of platelet adhesion observed by scanning electron microscopy (SEM) and the anticoagulant activity of the blood coagulant determined by testing plasma-clotting time. The control of grafting structures of PEGylated layers highly regulates the PVDF membrane to resist the adsorption of plasma proteins, the adhesion of platelets, and the coagulation of human plasma. It was found that PVDF membranes grafted with brush-like PEGylated layers presented higher hydration capability with binding water molecules than with network-like PEGylated layers to improve the hemocompatible character of plasma protein and blood platelet resistance in human blood. This work suggests that the hemocompatible nature of grafted PEGylated polymers by controlling grafting structures gives them great potential in the molecular design of antithrombogenic membranes for use in human blood.

Enhanced performance of dye-sensitized solar cells based on organic dopant incorporated PVDF-HFP/PEO polymer blend electrolyte with g-C3N4/TiO2 photoanode

International Nuclear Information System (INIS)

Senthil, R.A.; Theerthagiri, J.; Madhavan, J.; Murugan, K.; Arunachalam, Prabhakarn; Arof, A.K.

2016-01-01

This work describes the effect of 2-aminopyrimidine (2-APY) on poly(vinylidinefluoride-co-hexafluoropropylene) (PVDF-HFP)/polyethylene oxide (PEO) blend polymer electrolyte along with binary iodide salts (tetrabutylammonium iodide (TBAI) and potassium iodide (KI)) and iodine (I 2 ) were studied for enhancing the efficiency of the dye-sensitized solar cells (DSSCs) consisting of g-C 3 N 4 /TiO 2 composite as photoanode. The g-C 3 N 4 was synthesized from low cost urea by thermal condensation method. It was used as a precursor to synthesize the various weight percentage ratios (5%, 10% and 15%) of g-C 3 N 4 /TiO 2 composites by wet-impregnation method. The pure and 2-APY incorporated PVDF-HFP/PEO polymer blend electrolytes were arranged by wet chemical process (casting method) using DMF as a solvent. The synthesized g-C 3 N 4 /TiO 2 composites and polymer blend electrolytes were studied and analyzed by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffractometer (XRD) and scanning electron microscopy (SEM). The ionic conductivity values of the pure and 2-APY incorporated PVDF-HFP/PEO blend electrolytes were estimated to be 4.53×10 −5 and 1.87×10 −4 Scm −1 respectively. The UV–vis absorption spectroscopy was carried out for the pure and different wt% of g-C 3 N 4 /TiO 2 composites coated FTO films after N3 dye-sensitization. The 10 wt% g-C 3 N 4 /TiO 2 composite film showed a maximum absorption compared to the others. The DSSC assembled with 10 wt% g-C 3 N 4 /TiO 2 as photoanode using the pure polymer blend electrolyte exhibited a power conversion efficiency (PCE) of 3.17% , which was superior than that of DSSC based pure TiO 2 (2.46%). However, the PCE was increased to 4.73% for the DSSC assembled using 10 wt% g-C 3 N 4 /TiO 2 as photoanode with 2-APY incorporated polymer blend electrolyte. Hence, the present study is a successful attempt to provide a new pathway to enhance the performance of DSSCs. - Graphical abstract: In this study, the g-C 3 N

A Facile Strategy to Enhance the Dielectric and Mechanical Properties of MWCNTs/PVDF Composites with the Aid of MMA-co-GMA Copolymer

Science.gov (United States)

Song, Shixin; Xia, Shan; Jiang, Shangkun; Lv, Xue; Sun, Shulin; Li, Quanming

2018-01-01

A facile strategy is adopted to prepare carboxylic functionalized multiwalled carbon nanotube (c-MWCNT) modified high dielectric constant (high-k) poly(vinylidene fluoride) (PVDF) composites with the aid of methyl methacrylate-co-glycidyl methacrylate copolymer (MG). The MG is miscible with PVDF and the epoxy groups of the copolymer can react with the carboxylic groups of c-MWCNT, which induce the uniform dispersion of c-MWCNT and a form insulator layer on the surface of c-MWCNT. The c-MWCNTs/MG/PVDF composites with 8 vol % c-MWCNT present excellent dielectric properties with high dielectric constant (~448) and low dielectric loss (~2.36) at the frequency of 1 KHz, the dielectric loss is much lower than the c-MWCNT/PVDF composites without MG. The obvious improvement in dielectric properties ascribes to the existence of MG, which impede the direct contact of c-MWCNTs and PVDF and avoid the formation of conductive network. Therefore, we propose a practical and simple strategy for preparing composites with excellent dielectric properties, which are promising for applications in electronics devices. PMID:29495491

Activation of PVDF membranes through facile hydroxylation of the polymeric dope

KAUST Repository

Al-Gharabli, Samer; Mavukkandy, Musthafa O.; Kujawa, Joanna; Nunes, Suzana Pereira; Arafat, Hassan A.

2017-01-01

A method comprising a two-step alkali/acid treatment of poly (vinylidene fluoride) (PVDF) polymer is developed for the fabrication of flat-sheet PVDF membranes functionalized with labile hydroxyl groups. This method involves the application of a short-duration modification in alkali medium (5% KOH). Extensive characterizations were performed on the prepared membranes. Modification of the polymer altered the crystallinity of the PVDF from a mixture of both α and β phases to a predominant β phase. Lower work of adhesion of the modified membrane indicated the formation of a more hydrophobic and wetting-resistant membrane surface. Centrifugation of the polymer dope after the modification had a pronounced impact on the properties of the resultant membranes. This protocol could be utilized in fine-tuning the properties of PVDF membranes for various target-specific applications such as membrane distillation. This method can also be used in functionalizing PVDF membranes further by exploiting the labile –OH group present on the membrane surface.

Activation of PVDF membranes through facile hydroxylation of the polymeric dope

KAUST Repository

Al-Gharabli, Samer

2017-10-30

A method comprising a two-step alkali/acid treatment of poly (vinylidene fluoride) (PVDF) polymer is developed for the fabrication of flat-sheet PVDF membranes functionalized with labile hydroxyl groups. This method involves the application of a short-duration modification in alkali medium (5% KOH). Extensive characterizations were performed on the prepared membranes. Modification of the polymer altered the crystallinity of the PVDF from a mixture of both α and β phases to a predominant β phase. Lower work of adhesion of the modified membrane indicated the formation of a more hydrophobic and wetting-resistant membrane surface. Centrifugation of the polymer dope after the modification had a pronounced impact on the properties of the resultant membranes. This protocol could be utilized in fine-tuning the properties of PVDF membranes for various target-specific applications such as membrane distillation. This method can also be used in functionalizing PVDF membranes further by exploiting the labile –OH group present on the membrane surface.

Study on CO2/ N2 separation: the effect of rubbery polymer coating on PVDF membrane

Science.gov (United States)

Zuwairi, M. Z.; Rahman, S. A.

2017-06-01

The emission of harmful gases such as carbon dioxide (CO2) via gas processing plant and daily human activities gave negative impacts to the environment and global inhabitant. Flat sheet asymmetric membranes were produced from homogenous solution of Poly(vinylideneflouride) (PVDF) via phase inversion method using N-methyl-2-pyrrolidone (NMP) as the solvent. While the poly ether b-amide (PEBAX) was dissolve by using of (70 ethanol and 30 water) as a solvent and and lithium chloride as a additives. The morphology and cross section of the produced membranes were observed by Scanning Electron Microscope (SEM). Then, the membranes were tested for chemical analysis to define the presence of PEBAX in the membrane by using Fourier Transform Infrared (FTIR) spectroscopy. The permeation performances of the membranes were evaluated in terms of permeability and selectivity of the membranes by using gas permeation test. Increasing the PEBAX content significantly increased the selectivity of the PVDF membrane to separate the CO2/N2 gases but decreased the amount of the gases that passed through the membrane.

Preparation and characterization of biopolymers comprising chitosan-grafted-ENR via acid-induced reaction of ENR50 with chitosan

Directory of Open Access Journals (Sweden)

M. R. H. Mas Haris

2014-02-01

Full Text Available This paper describes the first detailed tailored-approach for the preparation of biopolymers comprising chitosan (CTS grafted onto the backbone of epoxidized natural rubber (CTS-g-ENR. In a typical experiment, appropriate amount of CTS and AlCl3•6H2O was added to a specified amount of ENR50 (ENR with about 50% epoxy content dissolved in a dual-solvent consisting of 1,4-dioxane and water (97.5:2.5% v/v and the resulting mixture refluxed with continuous stirring for 6 hours. Nuclear magnetic resonance (NMR spectral analysis of a biocomposite, CTS-g-ENR-P1, revealed that its epoxy content is 22.36% which is considerably lower than 44.93% as determined for ENR50-control (ENR50 derivative obtained under similar experimental condition but in the absence of CTS. This means that the grafting of CTS onto the backbone of ENR had occurred. The revelation is affirmed by the presence of the characteristic absorption bands of CTS and ENR, and the appearance of new bands at 1219, 902 and 733 cm–1 in the Fourier transform infrared (FTIR spectrum of CTS-g-ENR-P1. Further evidence that CTS had been successfully grafted onto the backbone of ENR can be deduced and described in this paper from the data obtained by means of Differential Scanning Calorimetric analysis, Thermogravimetric analysis and Variable Pressure Scanning Electron Microscopy.

Poly(ethylene-co-acrylic acid)-g-poly(ethylene glycol) graft copolymer templated synthesis of mesoporous TiO{sub 2} thin films for quasi-solid-state dye sensitized solar cells

Energy Technology Data Exchange (ETDEWEB)

Patel, Rajkumar; Jung, Ye Eun; Kim, Dong Jun; Kim, Sang Jin; Kim, Jong Hak, E-mail: jonghak@yonsei.ac.kr

2014-02-03

An amphiphilic graft copolymer, poly(ethylene-co-acrylic acid)-graft-poly(ethylene glycol) (PEAA-g-PEG), consisting of a PEAA backbone and PEG side chains was synthesized via an esterification reaction. {sup 1}H nuclear magnetic resonance and Fourier-transformed infrared analysis demonstrated esterification between carboxylic acid of PEAA and hydroxyl group of PEG. Small angle X-ray scattering results revealed that the crystalline domain spacing of PEAA increased from 11.3 to 12.8 nm upon using a more polar solvent with a higher affinity for poly(acrylic acid), while the crystalline domain spacing of PEAA disappeared with PEG grafting, indicating structural change to an amorphous state. Mesoporous TiO{sub 2} thin films were synthesized via a sol–gel reaction using PEAA-g-PEG graft copolymer as a structure-directing agent. The hydrophilically-preformed TiO{sub 2} nanoparticles were selectively confined in the hydrophilic PEG domains of the graft copolymer, and mesoporous TiO{sub 2} thin films were formed, as confirmed by scanning electron microscopy. The morphology of TiO{sub 2} films was tunable by varying the concentrations of polymer solutions and the amount of preformed TiO{sub 2}. A quasi-solid-state dye-sensitized solar cell fabricated with PEAA-g-PEG templated TiO{sub 2} film exhibited an energy conversion efficiency of 3.8% at 100 mW/cm{sup 2}, which was greater than that of commercially-available paste (2.6%) at a similar film thickness (3 μm). The improved performance was due to the larger surface area for high dye loading and organized structure with good interconnectivity. - Highlights: • Poly(ethylene-co-acrylic acid)-g-poly(ethylene glycol) (PEAA-g-PEG) graft copolymer is synthesized. • Amphiphilic PEAA-g-PEG acts as a structure directing agent. • Mesoporous TiO{sub 2} thin films are prepared by sol–gel reaction using PEAA-g-PEG template. • Efficiency of DSSC with templated TiO{sub 2} is greater than with commercial TiO{sub 2} paste.

In-situ infrared study of CO{sub 2} adsorption on SBA-15 grafted with {gamma}-(aminopropyl)triethoxysilane

Energy Technology Data Exchange (ETDEWEB)

Alex C.C. Chang; Steven S.C. Chuang; McMahan Gray; Yee Soong [University of Akron, Akron, OH (United States). Chemical Engineering Department

2003-04-01

CO{sub 2} adsorption/desorption on SBA-15 grafted with {gamma}-(aminopropyl)triethoxysilane (APTS) has been studied by infrared spectroscopy coupled with temperature-programmed desorption. SBA-15, a mesoporous silica material with a uniform pore size of 21 nm and a surface area of 200-230 m{sup 2}/g, provides an OH functional group for grafting of {gamma}-(aminopropyl)triethoxysilane. The amine-grafted SBA-15 adsorbed CO{sub 2} as carbonates and bicarbonates with a total capacity of 200-400 {mu}mol/g. The heat of CO{sub 2} desorption was determined to be 3.2-4.5 kJ/mol in the presence of H{sub 2}O and 6.6-11.0 kJ/mol in the absence of H{sub 2}O during temperature-programmed desorption. Repeated CO{sub 2} adsorption/desorption CO{sub 2} cycles shifted the desorption peak temperature downward and decreased the heat of CO{sub 2} adsorption. 22 refs., 9 figs., 3 tabs.

Radiation-induced grafting of styrene onto poly-vinylidene fluoride) film by simultaneous method with two different solvents

International Nuclear Information System (INIS)

Ferreira, H.P.; Parra, D.F.; Lugao, A.B.

2011-01-01

Complete text of publication follows. Radiation-induced grafting to create membranes with ion exchange capacity in fluorinated polymers has been studied for applications such as fuel cells, filtration and waste treatment and polymeric actuators due to their good physical and chemical properties. In this work, radiation-induced grafting of styrene into poly(vinylidene fluoride) (PVDF) films with 0.125 mm thickness at doses of 1 and 2.5 kGy in the presence of a styrene/N,N- dimethylformamide (DMF) solution (1:1, v/v) and at doses of 20, 40 and 80 kGy in presence of a styrene/toluene solution (1:1, v/v) at dose rate of 5 kGy h-1 was carried out by simultaneous method under nitrogen atmosphere and at room temperature, using gamma-rays form a Co-60. The films were characterized before and after modification by the grafting yield (GY), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and thermogravimetry (TG/DTG). GY results shows that grafting increases with dose, and it was possible to confirm the grafting of styrene by FT-IR due to the new characteristics peaks and by the TG and DSC due to changes in thermal behavior of the grafted material. Results showed that the system allows the homogeneous grafting of styrene into PVDF using gamma irradiation at doses as low as 1 kGy when DMF is used and heterogeneous grafting when toluene is used, showing the importance of the solvent nature during the simultaneous method.

Synthesis and electrochemical probing of water-soluble poly(sodium 4-styrenesulfonate-co-acrylic acid)-grafted multiwalled carbon nanotubes

International Nuclear Information System (INIS)

Du Feipeng; Yang Yingkui; Xie Xiaolin; Wu Kangbing; Gan Tian; Liu Lang

2008-01-01

Water-soluble poly(sodium 4-styrenesulfonate-co-acrylic acid)-grafted multiwalled carbon nanotubes (MWNT-g-P(SSS-co-AA)) with core-shell nanostructure were successfully synthesized by in situ free radical copolymerization of sodium 4-strenesulfonate (SSS) and acrylic acid (AA) in the presence of MWNTs terminated with vinyl groups; their structure was characterized by FTIR, 1 H NMR, Raman, TGA and TEM. The results showed that the thickness and content of the copolymer layer grafted onto the MWNT surface are about 7-12 nm and 82.3%, respectively. The P(SSS-co-AA) covalently grafted on MWNTs provides MWNT-g-P(SSS-co-AA) with good hydrophilicity and solubility in water. Then a novel MWNT-g-P(SSS-co-AA)-modified glassy carbon electrode was fabricated by coating; its electrochemical properties were evaluated by electrochemical probe of K 3 [Fe(CN) 6 ], and its catalytic behaviors to the electrochemical oxidation processes of dopamine (DA) and serotonin (5-HT) were investigated. Since the MWNT-g-P(SSS-co-AA)-modified electrode possesses strong electron transfer capability, high electrochemical activity and catalytic ability, it can be used in sensitive, selective, rapid and simultaneous monitoring of biomolecules

Preparation of polymer electrolyte membranes for lithium batteries by radiation-induced graft copolymerization

Energy Technology Data Exchange (ETDEWEB)

Nasef, Mohamed Mahmoud [Business and Advanced Technology Centre, Universiti Teknologi Malaysia, Jalan Semarak, 54100 Kuala Lumpur (Malaysia); Suppiah, Raja Rajeswary [Chemical Engineering Program, Universiti Teknologi Petronas, Bandar Seri Iskandar, 37150 Tronoh, Perak (Malaysia); Dahlan, Khairul Zaman Mohd [Malaysian Institute for Nuclear Technology Research, Bangi, 43000 Kajang (Malaysia)

2004-07-30

Polymer electrolyte membranes with different degrees of grafting were prepared by radiation-induced graft copolymerization of styrene monomer onto poly(vinylidene fluoride) (PVDF) films and subsequent chemical activation with liquid electrolyte consisting of lithium hexafluorophosphate (LiPF{sub 6}) in a mixture of ethylene carbonate/diethylene carbonate (EC/DEC). The chemical changes in the PVDF films after styrene grafting and subsequent chemical activation were monitored by FTIR spectroscopic analysis and the crystallinity was evaluated using differential scanning calorimetric (DSC) analysis. The swelling in electrolyte solution (electrolyte uptake) and the ionic conductivity of the membranes were determined at various degrees of grafting. The conductivity of the membranes was found to increase with the increase in the degree of grafting and reached a magnitude of 10{sup -3} S/cm at a degree of grafting of 50%. The results of this work suggest that radiation-induced graft polymerization provides an alternative method to substitute blending in preparation of polymer electrolyte membranes for application in lithium batteries.

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

Science.gov (United States)

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

2018-03-01

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

Proton exchange membranes based on PVDF/SEBS blends

Energy Technology Data Exchange (ETDEWEB)

Mokrini, A.; Huneault, M.A. [Industrial Materials Institute, National Research Council of Canada, 75 de Mortagne Blvd., Boucherville, Que. (Canada J4B 6Y4)

2006-03-09

Proton-conductive polymer membranes are used as an electrolyte in the so-called proton exchange membrane fuel cells. Current commercially available membranes are perfluorosulfonic acid polymers, a class of high-cost ionomers. This paper examines the potential of polymer blends, namely those of styrene-(ethylene-butylene)-styrene block copolymer (SEBS) and polyvinylidene fluoride (PVDF), in the proton exchange membrane application. SEBS/PVDF blends were prepared by twin-screw extrusion and the membranes were formed by calendering. SEBS is a phase-segregated material where the polystyrene blocks can be selectively functionalized offering high ionic conductivity, while PVDF insures good dimensional stability and chemical resistance to the films. Proton conductivity of the films was obtained by solid-state grafting of sulfonic acid moieties. The obtained membranes were characterized in terms of conductivity, ionic exchange capacity and water uptake. In addition, the membranes were characterized in terms of morphology, microstructure and thermo-mechanical properties to establish the blends morphology-property relationships. Modification of interfacial properties between SEBS and PVDF was found to be a key to optimize the blends performance. Addition of a methyl methacrylate-butyl acrylate-methyl methacrylate block copolymer (MMA-BA-MMA) was found to compatibilize the blend by reducing the segregation scale and improving the blend homogeneity. Mechanical resistance of the membranes was also improved through the addition of this compatibilizer. As little as 2wt.% compatibilizer was sufficient for complete interfacial coverage and lead to improved mechanical properties. Compatibilized blend membranes also showed higher conductivities, 1.9x10{sup -2} to 5.5x10{sup -3}Scm{sup -1}, and improved water management. (author)

Facile surface glycosylation of PVDF microporous membrane via direct surface-initiated AGET ATRP and improvement of antifouling property and biocompatibility

International Nuclear Information System (INIS)

Yuan Jing; Meng Jianqiang; Kang Yinlin; Du Qiyun; Zhang Yufeng

2012-01-01

This paper describes a facile and novel approach for the surface glycosylation of poly(vinylidene difluoride) (PVDF) microporous membrane. A glycopolymer poly(D-gluconamidoethyl methacrylate) (PGAMA) was tethered onto the membrane surface via activators generated by electron transfer atom transfer radical polymerization (AGET ATRP) directly initiated from the PVDF surface. Chemical changes of membrane surface were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). It was revealed that PGAMA was successfully grafted onto the membrane surface and its grafting density can be modulated in a wide range up to 2.4 μmol/cm 2 . The effects of glycosylation on membrane morphology, flux and surface hydrophilicity were investigated. Field emission scanning electron microscopy (FESEM) results indicated shrinkage of the surface pore diameters and the growth of the glycopolymer layer on the membrane surface. The static water contact angle (WCA) of the membrane surface decreased from 110° to 30.4° with the increase of grafting density, indicating that the PGAMA grafts dramatically improved the surface hydrophilicity. The protein adsorption and platelets adhesion experiments indicated that the grafted PGAMA could effectively improve the membrane antifouling property and biocompatibility.

Graft polymerization of acrylic acid and methacrylic acid onto poly(vinylidene fluoride) powder in presence of metallic salt and sulfuric acid

Science.gov (United States)

Deng, Bo; Yu, Yang; Zhang, Bowu; Yang, Xuanxuan; Li, Linfan; Yu, Ming; Li, Jingye

2011-02-01

Poly(vinylidene fluoride) (PVDF) powder was grafted with acrylic acid (AAc) or methacrylic acid (MAA) by the pre-irradiation induced graft polymerization technique. The presence of graft chains was proven by FT-IR spectroscopy. The degree of grafting (DG) was calculated by the acid-base back titration method. The synergistic effect of acid and Mohr's salt on the grafting kinetics was examined. The results indicated that adding sulfuric acid and Mohr's salt simultaneously in AAc or MAA solutions led to a strong enhancement in the degree of grafting. The grafted PVDF powder was cast into microfiltration (MF) membranes using the phase inversion method and some properties of the obtained MF membranes were characterized.

Graft polymerization of acrylic acid and methacrylic acid onto poly(vinylidene fluoride) powder in presence of metallic salt and sulfuric acid

Energy Technology Data Exchange (ETDEWEB)

Deng Bo [Shanghai Institute of Applied Physics, Chinese Academy of Sciences, No. 2019, Jialuo Road, Jiading Dist., 201800 Shanghai (China); Yu Yang; Zhang Bowu; Yang Xuanxuan [Shanghai Institute of Applied Physics, Chinese Academy of Sciences, No. 2019, Jialuo Road, Jiading Dist., 201800 Shanghai (China); Graduate University of Chinese Academy of Sciences, No. 19, Yuquan Road, Shijingshan Dist., 100049 Beijing (China); Li Linfan; Yu Ming [Shanghai Institute of Applied Physics, Chinese Academy of Sciences, No. 2019, Jialuo Road, Jiading Dist., 201800 Shanghai (China); Li Jingye, E-mail: jingyeli@sinap.ac.c [Shanghai Institute of Applied Physics, Chinese Academy of Sciences, No. 2019, Jialuo Road, Jiading Dist., 201800 Shanghai (China)

2011-02-15

Poly(vinylidene fluoride) (PVDF) powder was grafted with acrylic acid (AAc) or methacrylic acid (MAA) by the pre-irradiation induced graft polymerization technique. The presence of graft chains was proven by FT-IR spectroscopy. The degree of grafting (DG) was calculated by the acid-base back titration method. The synergistic effect of acid and Mohr's salt on the grafting kinetics was examined. The results indicated that adding sulfuric acid and Mohr's salt simultaneously in AAc or MAA solutions led to a strong enhancement in the degree of grafting. The grafted PVDF powder was cast into microfiltration (MF) membranes using the phase inversion method and some properties of the obtained MF membranes were characterized.

Graft polymerization of acrylic acid and methacrylic acid onto poly(vinylidene fluoride) powder in presence of metallic salt and sulfuric acid

International Nuclear Information System (INIS)

Deng Bo; Yu Yang; Zhang Bowu; Yang Xuanxuan; Li Linfan; Yu Ming; Li Jingye

2011-01-01

Poly(vinylidene fluoride) (PVDF) powder was grafted with acrylic acid (AAc) or methacrylic acid (MAA) by the pre-irradiation induced graft polymerization technique. The presence of graft chains was proven by FT-IR spectroscopy. The degree of grafting (DG) was calculated by the acid-base back titration method. The synergistic effect of acid and Mohr's salt on the grafting kinetics was examined. The results indicated that adding sulfuric acid and Mohr's salt simultaneously in AAc or MAA solutions led to a strong enhancement in the degree of grafting. The grafted PVDF powder was cast into microfiltration (MF) membranes using the phase inversion method and some properties of the obtained MF membranes were characterized.

Enhanced performance of dye-sensitized solar cells based on organic dopant incorporated PVDF-HFP/PEO polymer blend electrolyte with g-C{sub 3}N{sub 4}/TiO{sub 2} photoanode

Energy Technology Data Exchange (ETDEWEB)

Senthil, R.A.; Theerthagiri, J. [Solar Energy Lab, Department of Chemistry, Thiruvalluvar University, Vellore 632115 (India); Madhavan, J., E-mail: jagan.madhavan@gmail.com [Solar Energy Lab, Department of Chemistry, Thiruvalluvar University, Vellore 632115 (India); Murugan, K. [Department of Zoology, Bharathiar University, Coimbatore 641046 (India); Arunachalam, Prabhakarn [Electrochemistry Research Group, Chemistry Department, College of Science, King Saud University, Riyadh 11451 (Saudi Arabia); Arof, A.K. [Centre for Ionics University Malaya, Department of Physics, University of Malaya, Kuala Lumpur 50603 (Malaysia)

2016-10-15

This work describes the effect of 2-aminopyrimidine (2-APY) on poly(vinylidinefluoride-co-hexafluoropropylene) (PVDF-HFP)/polyethylene oxide (PEO) blend polymer electrolyte along with binary iodide salts (tetrabutylammonium iodide (TBAI) and potassium iodide (KI)) and iodine (I{sub 2}) were studied for enhancing the efficiency of the dye-sensitized solar cells (DSSCs) consisting of g-C{sub 3}N{sub 4}/TiO{sub 2} composite as photoanode. The g-C{sub 3}N{sub 4} was synthesized from low cost urea by thermal condensation method. It was used as a precursor to synthesize the various weight percentage ratios (5%, 10% and 15%) of g-C{sub 3}N{sub 4}/TiO{sub 2} composites by wet-impregnation method. The pure and 2-APY incorporated PVDF-HFP/PEO polymer blend electrolytes were arranged by wet chemical process (casting method) using DMF as a solvent. The synthesized g-C{sub 3}N{sub 4}/TiO{sub 2} composites and polymer blend electrolytes were studied and analyzed by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffractometer (XRD) and scanning electron microscopy (SEM). The ionic conductivity values of the pure and 2-APY incorporated PVDF-HFP/PEO blend electrolytes were estimated to be 4.53×10{sup −5} and 1.87×10{sup −4} Scm{sup −1} respectively. The UV–vis absorption spectroscopy was carried out for the pure and different wt% of g-C{sub 3}N{sub 4}/TiO{sub 2} composites coated FTO films after N3 dye-sensitization. The 10 wt% g-C{sub 3}N{sub 4}/TiO{sub 2} composite film showed a maximum absorption compared to the others. The DSSC assembled with 10 wt% g-C{sub 3}N{sub 4}/TiO{sub 2} as photoanode using the pure polymer blend electrolyte exhibited a power conversion efficiency (PCE) of 3.17% , which was superior than that of DSSC based pure TiO{sub 2} (2.46%). However, the PCE was increased to 4.73% for the DSSC assembled using 10 wt% g-C{sub 3}N{sub 4}/TiO{sub 2} as photoanode with 2-APY incorporated polymer blend electrolyte. Hence, the present study is a

Balsam-Pear-Skin-Like Porous Polyacrylonitrile Nanofibrous Membranes Grafted with Polyethyleneimine for Postcombustion CO2 Capture.

Science.gov (United States)

Zhang, Yufei; Guan, Jiming; Wang, Xianfeng; Yu, Jianyong; Ding, Bin

2017-11-22

Amine-containing sorbents have been extensively studied for postcombustion carbon dioxide (CO 2 ) capture because of their ability to chemisorb CO 2 from the flue gas. However, most sorbents are in the form of powders currently, which is not the ideal configuration for the flue gas separation because of the fragile nature and poor mechanical properties, resulting in blocking of the flow pipes and difficult recycling. Herein, we present a novel approach for the facile fabrication of flexible, robust, and polyethyleneimine-grafted (PEI-grafted) hydrolyzed porous PAN nanofibrous membranes (HPPAN-PEI NFMs) through the combination of electrospinning, pore-forming process, hydrolysis reaction, and the subsequent grafting technique. Excitingly, we find that all the resultant porous PAN (PPAN) fibers exhibit a balsam-pear-skin-like porous structure due to the selective removal of poly(vinylpyrrolidone) (PVP) from PAN/PVP fibers by water extraction. Significantly, the HPPAN-PEI NFMs retain their mesoporosity, as well as exhibit good thermal stability and prominent tensile strength (11.1 MPa) after grafting, guaranteeing their application in CO 2 trapping from the flue gas. When exposed to CO 2 at 40 °C, the HPPAN-PEI NFMs show an enhanced CO 2 adsorption capacity of 1.23 mmol g -1 (based on the overall quantity of the sample) or 6.15 mmol g -1 (based on the quantity of grafted PEI). Moreover, the developed HPPAN-PEI NFMs display significantly selective capture for CO 2 over N 2 and excellent recyclability. The CO 2 capacity retains 92% of the initial value after 20 adsorption-desorption cycle tests, indicating that the resultant HPPAN-PEI NFMs have good long-term stability. This work paves the way for fabricating NFM-based solid adsorption materials endowed with a porous structure applied to efficient postcombustion CO 2 capture.

Assessment of Blend PVDF Membranes, and the Effect of Polymer Concentration and Blend Composition

Directory of Open Access Journals (Sweden)

Imtiaz Ali

2018-03-01

Full Text Available In this work, PVDF homopolymer was blended with PVDF-co-HFP copolymer and studied in terms of morphology, porosity, pore size, hydrophobicity, permeability, and mechanical properties. Different solvents, namely N-Methyl-2 pyrrolidone (NMP, Tetrahydrofuran (THF, and Dimethylformamide (DMF solvents, were used to fabricate blended PVDF flat sheet membranes without the introduction of any pore forming agent, through a non-solvent induced phase separation (NIPS technique. Furthermore, the performance of the fabricated membranes was investigated for pressure and thermal driven applications. The porosity of the membranes was slightly increased with the increase in the overall content of PVDF and by the inclusion of PVDF copolymer. Total PVDF content, copolymer content, and mixed-solvent have a positive effect on mechanical properties. The addition of copolymer increased the hydrophobicity when the total PVDF content was 20%. At 25% and with the inclusion of mixed-solvent, the hydrophobicity was adversely affected. The permeability of the membranes increased with the increase in the overall content of PVDF. Mixed-solvents significantly improved permeability.

Assessment of Blend PVDF Membranes, and the Effect of Polymer Concentration and Blend Composition.

Science.gov (United States)

Ali, Imtiaz; Bamaga, Omar A; Gzara, Lassaad; Bassyouni, M; Abdel-Aziz, M H; Soliman, M F; Drioli, Enrico; Albeirutty, Mohammed

2018-03-05

In this work, PVDF homopolymer was blended with PVDF-co-HFP copolymer and studied in terms of morphology, porosity, pore size, hydrophobicity, permeability, and mechanical properties. Different solvents, namely N-Methyl-2 pyrrolidone (NMP), Tetrahydrofuran (THF), and Dimethylformamide (DMF) solvents, were used to fabricate blended PVDF flat sheet membranes without the introduction of any pore forming agent, through a non-solvent induced phase separation (NIPS) technique. Furthermore, the performance of the fabricated membranes was investigated for pressure and thermal driven applications. The porosity of the membranes was slightly increased with the increase in the overall content of PVDF and by the inclusion of PVDF copolymer. Total PVDF content, copolymer content, and mixed-solvent have a positive effect on mechanical properties. The addition of copolymer increased the hydrophobicity when the total PVDF content was 20%. At 25% and with the inclusion of mixed-solvent, the hydrophobicity was adversely affected. The permeability of the membranes increased with the increase in the overall content of PVDF. Mixed-solvents significantly improved permeability.

A two-step annealing process for enhancing the ferroelectric properties of poly(vinylidene fluoride) (PVDF) devices

KAUST Repository

Park, Jihoon

2015-01-01

We report a simple two-step annealing scheme for the fabrication of stable non-volatile memory devices employing poly(vinylidene fluoride) (PVDF) polymer thin-films. The proposed two-step annealing scheme comprises the crystallization of the ferroelectric gamma-phase during the first step and enhancement of the PVDF film dense morphology during the second step. Moreover, when we extended the processing time of the second step, we obtained good hysteresis curves down to 1 Hz, the first such report for ferroelectric PVDF films. The PVDF films also exhibit a coercive field of 113 MV m-1 and a ferroelectric polarization of 5.4 μC cm-2. © The Royal Society of Chemistry 2015.

Tunable Schottky diodes fabricated from crossed electrospun SnO{sub 2}/PEDOT-PSSA nanoribbons

Energy Technology Data Exchange (ETDEWEB)

Carrasquillo, Katherine V. [Department of Physics and Electronics, University of Puerto Rico-Humacao, Humacao, PR 00792 (Puerto Rico); Pinto, Nicholas J., E-mail: nicholas.pinto@upr.edu [Department of Physics and Electronics, University of Puerto Rico-Humacao, Humacao, PR 00792 (Puerto Rico)

2012-06-25

Graphical abstract: Crossed SnO{sub 2}/PEDOT-PSSA nanoribbon Schottky diodes. Highlight: Black-Right-Pointing-Pointer An inexpensive electrospinning technique is used to fabricate crossed nanoribbons of n-doped tin oxide and p-PEDOT. Black-Right-Pointing-Pointer Each intersection is a localized Schottky diode that is completely exposed to the environment after electrodes deposition. Black-Right-Pointing-Pointer This makes it useful as a gas and light sensor. Black-Right-Pointing-Pointer In addition, the ability to tune the diode parameters via a back gate truly makes this device multifunctional. Black-Right-Pointing-Pointer A half wave rectifier has been demonstrated with this device under UV illumination. - Abstract: Schottky diodes have been fabricated on doped Si/SiO{sub 2} substrates in air, by simply crossing individual electrospun tin oxide (SnO{sub 2}) and poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) (PEDOT-PSSA) nanoribbons. The conductivity of PEDOT-PSSA was {approx}6 S/cm with no observable field effect, while SnO{sub 2} exhibited n-doped field effect behavior with a charge mobility of {approx}3.1 cm{sup 2}/V-s. The diodes operate in air or in vacuum, under ambient illumination or in the dark, with low turn-on voltages and device parameters that are tunable via a back gate bias or a UV light source. Their unique design involves a highly localized active region that is completely exposed to the surrounding environment, making them potentially attractive for use as sensors. The standard thermionic emission model of a Schottky junction was applied to analyze the forward bias diode characteristics and was successfully tested as a half wave rectifier.

CdS decorated rGO containing PVDF electrospun fiber based piezoelectric nanogenerator for mechanical energy harvesting application

Science.gov (United States)

Roy, Krittish; Mandal, Dipankar

2018-04-01

In this work, we demonstrate a simple and facile route ofcadmium sulfide (CdS) nanoparticle (NPs) grafted reduced graphene oxide (rGO) synthesis. It is found that a pinch (0.25 wt%) of as synthesisedCdS/rGOnanocompositecan induce more than 90% of electroactive phases in the electrospunpoly(vinylidene fluoride) (PVDF) nanofiber. Moreover, CdS/rGO nanocomposite doped PVDF nanofiber based nanogenerator (NG) can generate an output voltage of approximately 4 V upon repetitive finger imparting. Thus, the NG can be used as a mechanical energy harvester and power source for portable electronic and optoelectronic wearable devices.

Zwitterionic sulfobetaine-grafted poly(vinylidene fluoride) membrane with highly effective blood compatibility via atmospheric plasma-induced surface copolymerization.

Science.gov (United States)

Chang, Yung; Chang, Wan-Ju; Shih, Yu-Ju; Wei, Ta-Chin; Hsiue, Ging-Ho

2011-04-01

Development of nonfouling membranes to prevent nonspecific protein adsorption and platelet adhesion is critical for many biomedical applications. It is always a challenge to control the surface graft copolymerization of a highly polar monomer from the highly hydrophobic surface of a fluoropolymer membrane. In this work, the blood compatibility of poly(vinylidene fluoride) (PVDF) membranes with surface-grafted electrically neutral zwitterionic poly(sulfobetaine methacrylate) (PSBMA), from atmospheric plasma-induced surface copolymerization, was studied. The effect of surface composition and graft morphology, electrical neutrality, hydrophilicity and hydration capability on blood compatibility of the membranes were determined. Blood compatibility of the zwitterionic PVDF membranes was systematically evaluated by plasma protein adsorption, platelet adhesion, plasma-clotting time, and blood cell hemolysis. It was found that the nonfouling nature and hydration capability of grafted PSBMA polymers can be effectively controlled by regulating the grafting coverage and charge balance of the PSBMA layer on the PVDF membrane surface. Even a slight charge bias in the grafted zwitterionic PSBMA layer can induce electrostatic interactions between proteins and the membrane surfaces, leading to surface protein adsorption, platelet activation, plasma clotting and blood cell hemolysis. Thus, the optimized PSBMA surface graft layer in overall charge neutrality has a high hydration capability and the best antifouling, anticoagulant, and antihemolytic activities when comes into contact with human blood. © 2011 American Chemical Society

Immobilization of catalase on poly(acrylonitrile)-g.co-hydroxyethyl methacrylate

International Nuclear Information System (INIS)

Cavaco, M.C.; Andrade, M.E.

1991-01-01

Various poly(acrylonitrile)-g.co-hydroxyethyl methacrylate graft copolymers were prepared by using gamma irradiation at 400 Gy.h -1 . The influence of monomer concentration and time of irradiation on the level of grafting were analysed. The hydrophilicity of the polymeric supports was calculated by determining the water sorption. From the results obtained, we could conclude that the hydrophilicity was dependent on the yield of grafting. Some of the graft copolymers prepared were used for the immobilization of catalase. This enzyme was covalently coupled to the hydroxyl groups of the support after activation either with epichlorohydrin or with p-toluene sulphonyl chloride. The yield of enzyme coupling increases when hexamethylenediamine was used as a 'spacer'. (author) 5 refs.; 3 figs.; 2 tabs

Preparation and Properties of Poly (vinylidene fluoride)/poly(dimethylsiloxane) graft (poly(propylene oxide)-block-poly(ethylene oxide)) blend porous separators and corresponding electrolytes

International Nuclear Information System (INIS)

Li, Hao; Zhang, Hong; Liang, Zhi-Ying; Chen, Yue-Ming; Zhu, Bao-Ku; Zhu, Li-Ping

2014-01-01

Highlights: •This work aims exploring microporous PVDF separators for lithium ion batteries. •Comb structure polymer PDMS-g-(PPO-PEO) was used in PVDF blend separators. •The influence of polyether side chains on interfacial resistance was studied. -- Abstract: This work aims exploring the high performance porous separators that can be activated into gel electrolyte membranes for lithium ion batteries. A comb-like copolymer poly (dimethylsiloxane) graft poly (propylene oxide)-block-poly (ethylene oxide) (PDMS-g-(PPO-PEO)) was synthesized and blended with poly (vinylidene fluoride) (PVDF) to fabricate porous separators via a typical phase inversion process, and then the separators absorbed liquid electrolyte solution and formed into polymer electrolyte membranes. By measuring the composition, morphology and ion conductivity etc, the influence of PDMS-g-(PPO-PEO) on structure and properties of blend separators were discussed. Compared with pure PVDF separator with comparable porous structure, the adoption of PDMS-g-(PPO-PEO) decreased the crystallinity and increased the liquid electrolyte uptake and stability effectively. It was also found that the electrode/electrolyte interfacial resistance could be reduced greatly. The resulting electrolyte membrane using separator with PVDF/PDMS-g-(PPO-PEO) mass ratio in 8/2 exhibited highest ionic conductivity in 4.5 × 10 −3 S/cm at room temperature, while the electrochemical stability was up to 4.7 V (vs. Li/Li + ). Coin cells assembled with such separators also exhibited stable cycle performance and improved rate capabilities, especially when discharge rate higher than 0.5 C

Influence of silane coupling agent on microstructure and properties of CCTO-P(VDF-CTFE composites

Directory of Open Access Journals (Sweden)

Yang Tong

2018-04-01

Full Text Available Influence of the coupling agent on microstructure and dielectric properties of ceramic–polymer composites is systematically studied using CaCu3Ti4O12 (CCTO as the filler, trichloro-(1H,1H,2H,2H-perfluorooctyl-silane (Cl3-silane as coupling agent, and P(VDF-CTFE 88/12mol.% copolymer as the matrix. It is demonstrated that Cl3-silane molecules can be attached onto CCTO surface using a simple process. The experimental results show that coating CCTO with Cl3-silane can improve the microstructure uniformity of the composites due to the good wettability between Cl3-silane and P(VDF-CTFE, which also significantly improves the electric breakdown field of the composites. It is found that the composites using CCTO coated with 1.0wt.% Cl3-silane exhibit a higher dielectric constant with a higher electric breakdown field. For the composites with 15vol.% CCTO that is coated with 1.0wt.% Cl3-silane, an electric breakdown field of more than 240MV/m is obtained with an energy density of more than 4.5J/cm3. It is also experimentally found that the dielectric constant can be used to easily identify the optimized content of coupling agent.

Influence of silane coupling agent on microstructure and properties of CCTO-P(VDF-CTFE) composites

Science.gov (United States)

Tong, Yang; Zhang, Lin; Bass, Patrick; Rolin, Terry D.; Cheng, Z.-Y.

Influence of the coupling agent on microstructure and dielectric properties of ceramic-polymer composites is systematically studied using CaCu3Ti4O12 (CCTO) as the filler, trichloro-(1H,1H,2H,2H-perfluorooctyl)-silane (Cl3-silane) as coupling agent, and P(VDF-CTFE) 88/12mol.% copolymer as the matrix. It is demonstrated that Cl3-silane molecules can be attached onto CCTO surface using a simple process. The experimental results show that coating CCTO with Cl3-silane can improve the microstructure uniformity of the composites due to the good wettability between Cl3-silane and P(VDF-CTFE), which also significantly improves the electric breakdown field of the composites. It is found that the composites using CCTO coated with 1.0wt.% Cl3-silane exhibit a higher dielectric constant with a higher electric breakdown field. For the composites with 15vol.% CCTO that is coated with 1.0wt.% Cl3-silane, an electric breakdown field of more than 240MV/m is obtained with an energy density of more than 4.5J/cm3. It is also experimentally found that the dielectric constant can be used to easily identify the optimized content of coupling agent.

Ferroelectric Phase Diagram of PVDF:PMMA

OpenAIRE

Li, Mengyuan; Stingelin, Natalie; Michels, Jasper J.; Spijkman, Mark-Jan; Asadi, Kamal; Feldman, Kirill; Blom, Paul W. M.; de Leeuw, Dago M.

2012-01-01

We have investigated the ferroelectric phase diagram of poly(vinylidene fluoride) (PVDF) and poly(methyl methacrylate) (PMMA). The binary nonequilibrium temperature composition diagram was determined and melting of alpha- and beta-phase PVDF was identified. Ferroelectric beta-PVDF:PMMA blend films were made by melting, ice quenching, and subsequent annealing above the glass transition temperature of PMMA, close to the melting temperature of PVDF. Addition of PMMA suppresses the crystallizatio...

Effect of Compatibilization on Poly-ε-Caprolactone Grafting onto Poly(ethylene-co-vinyl alcohol

Directory of Open Access Journals (Sweden)

Mohamed Taha

2011-10-01

Full Text Available The non-miscibility of the reactants during solvent free poly-ε-caprolactone grafting onto poly(ethylene-co-vinyl alcohol (EVOH dramatically affects reaction kinetics. Different solutions were proposed to accelerate the exchange reactions between poly(ethylene-co-vinyl alcohol and poly-ε-caprolactone. Reactions were conducted in a batch reactor or a mini twin-screw extruder. The addition of a poly(ethylene-co-vinyl alcohol-g-poly-ε-caprolactone copolymer increased the compatibility of the reactants and led to a higher reaction rate. This copolymer was either prepared separately and added at the reaction beginning or prepared in situ grafting caprolactone from EVOH. The reactive system evolution was analyzed using molar mass evolution, microstructure characterization, thermal properties and the reactive blend morphology. The compatibilization effect combined with optimized reaction conditions, such as concentration and nature of catalyst and temperature, resulted in an important increase in reaction rates. Among the tested catalysts, 1,5,7-Triazabicyclo [4.4.0]dec-5-ene was a more efficient catalyst for grafting reactions than Tin (II 2-ethylhexanoate.

Solid-state-processing of d_PVDF

OpenAIRE

Martín, Jaime; Zhao, Dong; Lenz, Thomas; Katsouras, Ilias; de Leeuw, Dago M.; Stingelin, Natalie

2017-01-01

Poly(vinylidene fluoride) (PVDF) has long been regarded as an ideal piezoelectric plastic because it exhibits a large piezoelectric response and a high thermal stability. However, the realization of piezoelectric PVDF elements has proven to be problematic, amongst others, due to the lack of industrially-scalable methods to process PVDF into the appropriate polar crystalline forms. Here, we show that fully piezoelectric PVDF films can be produced via a single-step process that exploits the fac...

Blood compatibility assessment of graft copolymer (NR-g-DMAA) tubes

International Nuclear Information System (INIS)

Razzak, M.T.; Otsuhata, Kazushige; Tabata, Yoneho; Ohashi, Fumio; Takeuchi, Atsuki

1992-01-01

Graft copolymer (NR-g-DMAA) tubes have been prepared using simultaneous radiation induced grafting of N,N-dimethyl-acrylamide, (DMAA) onto natural rubber (NR) tubes. The blood compatibility of the NR-g-DMAA tubes was assessed with three methods, namely in vitro test, ex vivo once through test and ex vivo loops test. In the case of the in vitro test, a simple whole blood contacting procedure has been employed. The ex vivo once through test involves the exposing of NR-g-DMAA tubes with once through flow of fresh canine blood and then it was inspected for any evidence of clot. In the case of ex vivo loops test, the NR-g-DMAA tube was implanted at external jugular vein of a mongrel canine and the blood flow in the NR-g-DMAA tube was detected with an ultrasonic flow meter. It was found that the blood compatibility of NR-g-DMAA tubes is improved significantly with the increasing degree of grafting. All the NR-g-DMAA tubes having a degree of grafting of about 30 wt% or more exhibit good blood compatibility. It was found that the blood compatibility of the NR-g-DMAA tube is better than that of a medical grade silicon rubber (SiR) tube. (Author)

Swelling properties of cassava starch grafted with poly (potassium acrylate-co-acrylamide) superabsorbent hydrogel prepared by ionizing radiation

Science.gov (United States)

Barleany, Dhena Ria; Ulfiyani, Fida; Istiqomah, Shafina; Heriyanto, Heri; Rahmayetty, Erizal

2015-12-01

Natural and synthetic hydrophylic polymers can be phisically or chemically cross-linked in order to produce hydrogels. Starch based hydrogels grafted with copolymers from acrylic acid or acrylamide have become very popular for water absorbent application. Superabsorbent hydrogels made from Cassava starch grafted with poly (potassium acrylate-co-acrylamide) were prepared by using of ϒ-irradiation method. Various important parameters such as irradiation doses, monomer to Cassava starch ratio and acrylamide content were investigated. The addition of 7,5 % w w-1 acrylamide into the reaction mixture generated a starch graft copolymer with a water absorption in distilled water as high as 460 g g-1 of its dried weight. The effectivity of hydrogel as superabsorbent for aqueous solutions of NaCl and urea was evaluated. The obtained hydrogel showed the maximum absorptions of 317 g g-1 and 523 g g-1 for NaCl and urea solution, respectively (relative to its own dry weight). The structure of the graft copolymer was analyzed by using Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscope (SEM).

Kinetic investigations of graft copolymerization of sodium styrene sulfonate onto electron beam irradiated poly(vinylidene fluoride) films

Energy Technology Data Exchange (ETDEWEB)

Mahmoud Nasef, Mohamed, E-mail: mahmoudeithar@fkkksa.utm.m [Institute of Hydrogen Economy, International City Campus, Universiti Teknologi Malaysia, Jalan Semarak, 54100 Kuala Lumpur (Malaysia); Chemical Engineering Department, Faculty of Chemical and Natural Resources Engineering, Universiti Teknologi Malaysia, 81310 UTM Skudai, Johor (Malaysia); Saidi, Hamdani [Institute of Hydrogen Economy, International City Campus, Universiti Teknologi Malaysia, Jalan Semarak, 54100 Kuala Lumpur (Malaysia); Chemical Engineering Department, Faculty of Chemical and Natural Resources Engineering, Universiti Teknologi Malaysia, 81310 UTM Skudai, Johor (Malaysia); Mohd Dahlan, Khairul Zaman [Radiation Processing Technology Division, Malaysian Nuclear Agency, Bangi, 43000 Kajang, Selangor (Malaysia)

2011-01-15

Graft copolymerization of sodium styrene sulfonate (SSS) onto electron beam (EB) irradiated poly(vinylidene fluoride) (PVDF) films was investigated to find out a simple preparation process for sulfonic acid proton exchange membranes with respect to monomer concentration, absorbed dose, temperature, film thickness and storage time. The reaction order of the monomer concentration and absorbed dose of grafting was found to be 2.84 and 1.20, respectively. The overall activation energy for graft copolymerization reaction was calculated to be 11.36 kJ/mol. The initial rate of grafting was found to decrease with an increase in the film thickness. The trapped radicals in the irradiated PVDF films remained effective in initiating the reaction without considerable loss in grafting level up to 180 days, when stored under -60 {sup o}C. The presence and distribution of polystyrene sulfonate grafts in the obtained membranes were observed by Fourier transform infrared (FTIR) spectroscopic analysis, scanning optical microscope and scanning transmission electron microscopy (STEM) coupled with X-ray energy dispersive (EDX), respectively.

A multifunctional PVDF-based tactile sensor for minimally invasive surgery

Science.gov (United States)

Sokhanvar, S.; Packirisamy, M.; Dargahi, J.

2007-08-01

In this paper a multifunctional tactile sensor system using PVDF (polyvinylidene fluoride), is proposed, designed, analyzed, tested and validated. The working principle of the sensor is in such a way that it can be used in combination with almost any end-effectors. However, the sensor is particularly designed to be integrated with minimally invasive surgery (MIS) tools. In addition, the structural and transduction materials are selected to be compatible with micro-electro-mechanical systems (MEMS) technology, so that miniaturization would be possible. The corrugated shape of the sensor ensures the safe tissue grasping and compatibility with the traditional tooth-like end effectors of MIS tools. A unit of this sensor comprised of a base, a flexible beam and three PVDF sensing elements. Two PVDF sensing elements sandwiched at the end supports work in thickness mode to measure the magnitude and position of applied load. The third PVDF sensing element is attached to the beam and it works in the extensional mode to measure the softness of the contact object. The proposed sensor is modeled both analytically and numerically and a series of simulations are performed in order to estimate the characteristics of the sensor in measuring the magnitude and position of a point load, distributed load, and also the softness of the contact object. Furthermore, in order to validate the theoretical results, the prototyped sensor was tested and the results are compared. The results are very promising and proving the capability of the sensor for haptic sensing.

Preparation of poly(vinylbenzyl chloride)-grafted PFA film by a simultaneous irradiation grafting method

International Nuclear Information System (INIS)

Fei, Geng; Shin, Jun Hwa; Nho, Young Chang; Lee, Youn Sik

2009-01-01

In this study, PFA-g-PVBC films were prepared by a radiation grafting of vinylbenzyl chloride (VBC) monomer onto poly(tetrafluoroethylene-co-perfluoro propyl vinyl ether) (PFA) films by simultaneous irradiation method. IR, TGA, and SEM-EDX instruments were utilized to confirm the successful preparation of the grafted film. The effects of several irradiation conditions, including the dose, VBC concentration, and film thickness on the degree of grafting of PFA-g-PVBC film were investigated

Grafting of acrylamide onto synthetic co polyamide by gamma irradiation

Energy Technology Data Exchange (ETDEWEB)

Hamoud, M R; Qamhieyh, E A [Chemistry Dept., College of Ibn Al-Haitham Baghdad university-Adhamiyah-Baghdad- (Iraq)

1995-10-01

Grafted copolymer was prepared by using gamma irradiation to graft acrylamide onto polymeric molecule prepared by interfacial condensation between two diamine molecules like 1,2 diamino propane and 1,6 diamino-hexane in aqueous layer with sebacoyl chloride in organic layer. The resulted co polyamide was grafted with acrylamide using gamma irradiation. The optimum conditions of grafting reaction were found, also various factors such as the effect of solvents, redox systems and the role water on the radiochemical grafting were studied. Many techniques were used in the characterization of the copolymer before and after grafting. 8 figs.,.

Radiation-induced grafting of acrylamide onto guar gum in aqueous medium: Synthesis and characterization of grafted polymer guar-g-acrylamide

Energy Technology Data Exchange (ETDEWEB)

Biswal, Jayashree [Radiation Technology Development Section, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India); Kumar, Virendra [Radiation Technology Development Section, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India); Bhardwaj, Y.K. [Radiation Technology Development Section, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India)]. E-mail: ykbhard@magnum.barc.ernet.in; Goel, N.K. [Radiation Technology Development Section, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India); Dubey, K.A. [Radiation Technology Development Section, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India); Chaudhari, C.V. [Radiation Technology Development Section, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India); Sabharwal, S. [Radiation Technology Development Section, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India)

2007-10-15

Mutual radiation grafting technique has been applied to carry out grafting of acrylamide (AAm) onto guar gum (GG) using high-energy Co{sup 60} {gamma} radiation to enhance its flocculating properties for industrial effluents. The grafted product was characterized using analytical probes like elemental analysis, thermal analysis, Fourier transformed infrared (FTIR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The grafting extent was observed to decrease with the dose rate and increase with the concentration of AAm. Thermo gravimetric analysis (TGA) of grafted and ungrafted samples indicated better stability of grafted product. {gamma} and microwave radiation effect on grafted and virgin GG has also been reported.

Use of gamma and UV radiation in grafting hydrogel polymers to membranes

International Nuclear Information System (INIS)

Baker, L.; Hill, D.J.T.; Whittaker, A.; Hunter, D.; Davis, T.P.

1998-01-01

Full text: Dimethylacrylamide and N-isopropylacrylamide hydrogels are useful for their ability to absorb large amounts of water and for their thermotropic response. However as membranes they do not have the mechanical properties to be applicable in industry. Therefore these hydrogels have been grafted to polyvinylidinedifluoride (PVDF) membranes using radiation. Both UV and gamma irradiation were used. In the first method the PVDF membranes were first hydroxylated by immersion in a aqueous solution of potassium peroxydisulfate (10% w/v), with nitrogen purging for two hours at 80 deg C. This was followed by immersion in an aqueous solution of riboflavine (4mg/L) and monomer (10% v/v), degassing with nitrogen and irradiation under a Mercury UV light (wavelength 240 nm) at room temperature for 15 minutes. Membranes were washed by soxhlet extraction in distilled water and oven dried. The second method of grafting hydrogels to membranes involved immersing the membrane in 10 mL of distilled water containing monomer and CuSO 4 to prevent homopolymerisation. The solution was degassed with N 2 for 3 minutes then irradiated under nitrogen using a 60 Co source for various time periods. The effect of varying monomer and CuSO 4 concentration as well as dose rate and dose were studied. Membranes were rinsed in distilled water for 24 hours and dried in an oven before characterisation. Grafting was characterised by mass change (Mettler AC 100 balance), XPS (PHI Model 560 XPS/SAM/SIMA1 multitechnique surface analysis system), SEM (Hitachi S-900 Field Emission SEM) and FTIR-ATR (Perkn Elmer System 2000 FTIR with MIRMCT detector)

Surface modification of poly(vinylidene fluoride) membrane with hydrophilic and anti-fouling performance via a two-step polymerization

Energy Technology Data Exchange (ETDEWEB)

Chen, Gui-E; Sun, Li; Huang, Hui-Hong; Liu, Yan-Jun [Shanghai Institute of Technology, Shanghai (China); Xu, Zhen-Liang; Yang, Hu [East China University of Science and Technology, Shanghai (China)

2015-12-15

The surface modification of poly (vinylidene fluoride) (PVDF) membrane was performed via a two-step polymerization reactions. Poly (acrylic acid) (PAAc) was first grafted onto the membrane surface for the preparation of PVDF-g-PAAc membrane, and then poly (ethylene glycol) 200 (PEG 200) was immobilized on the membrane surface by the esterification reaction for the fabrication of PVDF-g-PEGA membrane. Attenuated total reflectance (ATR) FTIR, X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), and protein adsorption, water flux, water content and dynamic contact angle were conducted to characterize the structures and performance of the resultant PVDF membranes. The experimental results showed that the adsorption of bovine serum albumin (BSA) on the PVDF-g-PEGA membrane decreased about 80% when the grafting ratio reached to 15 wt%, compared with the pristine PVDF membrane. Moreover, the water contact angle of the membrane dropped to 60.5o, while the membrane pore sizes remained little changed.

Swelling properties of cassava starch grafted with poly (potassium acrylate-co-acrylamide) superabsorbent hydrogel prepared by ionizing radiation

Energy Technology Data Exchange (ETDEWEB)

Barleany, Dhena Ria, E-mail: dbarleany@yahoo.com; Ulfiyani, Fida; Istiqomah, Shafina; Rahmayetty [Department of Chemical Engineering, University of Sultan Ageng Tirtayasa, Cilegon, Banten (Indonesia); Heriyanto, Heri; Erizal [Centre for Application of Isotopes and Radiation, Jakarta (Indonesia)

2015-12-29

Natural and synthetic hydrophylic polymers can be phisically or chemically cross-linked in order to produce hydrogels. Starch based hydrogels grafted with copolymers from acrylic acid or acrylamide have become very popular for water absorbent application. Superabsorbent hydrogels made from Cassava starch grafted with poly (potassium acrylate-co-acrylamide) were prepared by using of ϒ-irradiation method. Various important parameters such as irradiation doses, monomer to Cassava starch ratio and acrylamide content were investigated. The addition of 7,5 % w w{sup −1} acrylamide into the reaction mixture generated a starch graft copolymer with a water absorption in distilled water as high as 460 g g{sup −1} of its dried weight. The effectivity of hydrogel as superabsorbent for aqueous solutions of NaCl and urea was evaluated. The obtained hydrogel showed the maximum absorptions of 317 g g{sup −1} and 523 g g{sup −1} for NaCl and urea solution, respectively (relative to its own dry weight). The structure of the graft copolymer was analyzed by using Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscope (SEM)

The study on grafting comonomer of n-butyl acrylate and styrene onto poly(ethylene terephthalate) film by gamma-ray induced graft copolymerization

Energy Technology Data Exchange (ETDEWEB)

Ping Xiang; Wang Mozhen [CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026 (China); Ge Xuewu, E-mail: xwge@ustc.edu.c [CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026 (China)

2010-09-15

Poly(ethylene terephthalate) (PET) film was successfully grafted with n-butyl acrylate and styrene comonomer through gamma-ray induced graft copolymerization. The degree of grafting (DG) and the composition of grafted side chain were characterized by {sup 1}H NMR. It was found that St can inhibit the homopolymerization of BA effectively and increase the DG when the concentration of comonomer mixture is kept constant. The proportion of St to BA in grafted side chain has a positive dependence on the feed ratio of St, which ultimately approaches the feed ratio. The thermal properties of poly(ethylene terephthalate)-graft-poly(n-butyl acrylate-co-styrene) (PET-g-P(BA-co-St)) films were investigated by differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA). The T{sub g} of PET decreases with the DG, indicating that the grafted P(BA-co-St) copolymer has good compatibility with PET backbone.

A two-step annealing process for enhancing the ferroelectric properties of poly(vinylidene fluoride) (PVDF) devices

KAUST Repository

Park, Jihoon; Kurra, Narendra; AlMadhoun, M. N.; Odeh, Ihab N.; Alshareef, Husam N.

2015-01-01

We report a simple two-step annealing scheme for the fabrication of stable non-volatile memory devices employing poly(vinylidene fluoride) (PVDF) polymer thin-films. The proposed two-step annealing scheme comprises the crystallization

Submicroscopic pores grafted using the residual sites produced by swift heavy ions

International Nuclear Information System (INIS)

Mazzei, R.; Betz, N.; Bermudez, G. Garcia; Massa, G.; Smolko, E.

2005-01-01

To produce nuclear track membranes (NTM) with submicroscopic pores poly(vinylidene difluoride) (PVDF) foils were irradiated with Cl, Ag and Pb ions. Then they were chemically etched for different times and grafted with acrylic acid. The grafting yields were determined by weight measurements as a function of ion fluence, etching time and also analysed using Fourier transform infrared spectroscopy. Both measurements suggest that the acrylic acid was grafted on the pore wall of the NTM using the active sites left by the ion beam

Flexible PVDF ferroelectric capacitive temperature sensor

KAUST Repository

Khan, Naveed

2015-08-02

In this paper, a capacitive temperature sensor based on polyvinylidene fluoride (PVDF) capacitor is explored. The PVDF capacitor is characterized below its Curie temperature. The capacitance of the PVDF capacitor changes vs temperature with a sensitivity of 16pF/°C. The linearity measurement of the capacitance-temperature relation shows less than 0.7°C error from a best fit straight line. An LC oscillator based temperature sensor is demonstrated based on this capacitor.

Surface modification of cation exchange membranes by graft polymerization of PAA-co-PANI/MWCNTs nanoparticles

International Nuclear Information System (INIS)

Nemati, Mahsa; Hosseini, Sayed Mohsen; Bagheripour, Ehsan; Madaeni, Sayed Siavash

2016-01-01

Surface modification of polyvinylchloride based heterogeneous cation exchange membrane was performed by graft polymerization of PAA and PAA-co-PANI/MWCNTs nanoparticles. The ion exchange membranes were prepared by solution casting technique. Spectra analysis confirmed graft polymerization clearly. SEM images illustrated that graft polymerization covers the membranes by simple gel network entanglement. The membrane water content was decreased by graft polymerization of PAA-co-PANI/MWCNTs nanoparticles on membrane surface. Membrane transport number and selectivity declined initially by PAA graft polymerization and then began to increase by utilizing of composite nanoparticles in modifier solution. The sodium and barium flux was improved sharply by PAA and PAAco- 0.01%wt PANI/MWCNTs graft polymerization on membrane surface and then decreased again by more increase of PANI/MWCNTs nanoparticles content ratio in modifier solution. The electrodialysis experiment results in laboratory scale showed higher dialytic rate in heavy metals removal for grafted-PAA and grafted-PAA-co-PANI/MWCNTs modified membrane compared to pristine one. Membrane areal electrical resistance was also decreased by introducing graft polymerization of PAA and PAA-co-PANI/MWCNTs NPs on membrane surface.

Potassium fulvate as co-interpenetrating agent during graft polymerization of acrylic acid from cellulose.

Science.gov (United States)

Ghazy, Mohamed B M; El-Hai, Farag Abd; Mohamed, Magdy F; Essawy, Hisham A

2016-10-01

Grafting polymerization of acrylic acid onto cellulose in presence of potassium fulvate (KF) as a co-interpenetrating agent results enhanced water sorption compared to materials prepared similarly in its absence. The insertion of potassium fulvate (KF) did not affect the grafting process and is thought to proceed in parallel to the graft polymerization via intensive polycondensation reactions of its function groups (-COOH and OH) with COOH of the monomer and OH groups of cellulose. The combination of graft copolymerization and polycondensation reactions is assumed to produce interpenetrating network structure. Fourier transform infrared (FTIR) confirmed successful incorporation within the network structure which is an evidence for formation of interpenetrating network. The obtained structures showed homogeneous uniform surface as revealed by scanning electron microscopy (SEM). The obtained superabsorbent possessed high water absorbency 422 and 48.8g/g in distilled water and saline (0.9wt.% NaCl solution), respectively, and enhanced water retention even at elevated temperatures as revealed by thermogravimetric analysis (TGA). This could be explained by the high content of hydrophilic groups. The new superabsorbents proved to be efficient devices for controlled release of fertilizers which expands their use in agricultural applications. Copyright © 2016 Elsevier B.V. All rights reserved.

Graft polymerization of vinyl acetate onto starch. Saponification to starch-g-poly(vinyl alcohol)

International Nuclear Information System (INIS)

Fanta, G.F.; Burr, R.C.; Doane, W.M.; Russell, C.R.

1979-01-01

Graft polymerizations of vinyl acetate onto granular cornstarch were initiated by cobalt-60 irradiation of starch-monomer-water mixtures, and ungrafted poly(vinyl acetate) was separated from the graft copolymer by benzene extraction. Conversions of monomer to polymer were quantitative at a radiation dose of 1.0 Mrad. Over half of the polymer was present as ungrafted poly(vinyl acetate) (grafting efficiency less than 50%), and the graft copolymer contained only 34% grafted synthetic polymer (34% add-on). Lower irradiation doses produced lower conversions of monomer to polymer and gave graft copolymers with lower % add-on. Addition of minor amounts of acrylamide, methyl acrylate, and methacrylic acid as comonomers produced only small increases in % add-on and grafting efficency. Grafting efficiency was increased to 70% when a monomer mixture containing about 10% methyl methacrylate was used. Grafting efficiency could be increased to over 90% if the graft polymerization of vinyl acetate--methyl methacrylate was carried out near 0 0 C; although conversion of monomers to polymer was low and grafted polymer contained 40 to 50% poly(methyl methacrylate). Selected graft copolymers were treated with methanolic sodium hydroxide to convert starch-g-poly(vinyl acetate) to starch-g-poly(vinyl alcohol). The molecular weight of the poly(vinyl alcohol) moiety was about 30,000. The solubility of starch-g-poly(vinyl alcohol) in hot water was less than 50; however, solubility could be increased by substituting either acid-modified or hypochlorite-oxidized for unmodified starch in the graft polymerization reaction. Vinyl acetate was also graft polymerized onto acid-modified starch which had been dispersed and partially solubilized by heating in water. A total irradiation dose of either 1.0 or 0.5 Mrad gave starch-g-poly

The Application of PVDF in Converter Cooling Pipeline

Science.gov (United States)

Geng, Man; Lu, Zhimin

2017-11-01

The structure, mechanical property, thermodynamics property, electrical aspects, radiation property and chemical property were introduced, and PVDF could satisfy the requirement of converter cooling pipe. PVDF department and pipe of distribution pipeline of converter cooling system in Debao HVDC project are used to introduce the molding process of PVDF.

Polymethacrylic acid grafted psyllium (Psy- g-PMA): a novel material for waste water treatment

Science.gov (United States)

Kumar, Ranvijay; Sharma, Kaushlendra; Tiwary, K. P.; Sen, Gautam

2013-03-01

Polymethacrylic acid grafted psyllium (Psy- g-PMA) was synthesized by microwave assisted method, which involves a microwave irradiation in synergism with silver sulfate as a free radical initiator to initiate grafting reaction. Psy- g-PMA grades have been synthesized and characterized on structural basis (elemental analysis, FTIR spectroscopy, intrinsic viscosity study) as well as morphological and thermal studies, taking psyllium as reference. The effects of reaction time, amount of monomer and silver sulfate (free radical initiator) on grafting of PMA on psyllium backbone have been studied. It is observed that all the grades of Psy- g-PMA have higher intrinsic viscosities than that of psyllium. The best synthesized grade was Psy- g-PMA having intrinsic viscosity of 6.93 and 58 % grafting of PMA on the main polymer backbone. Further Psy- g-PMA applications as flocculants for waste water treatment have been investigated. Psy- g-PMA resulted in higher decrease in the flocculation parameters such as total dissolved solid or total solids compared to psyllium. Hence the result shows the possible application of grafted psyllium in wastewater treatment.

Enhanced CO2 Adsorption on Activated Carbon Fibers Grafted with Nitrogen-Doped Carbon Nanotubes

Directory of Open Access Journals (Sweden)

Yu-Chun Chiang

2017-05-01

Full Text Available In this paper, multiscale composites formed by grafting N-doped carbon nanotubes (CNs on the surface of polyamide (PAN-based activated carbon fibers (ACFs were investigated and their adsorption performance for CO2 was determined. The spaghetti-like and randomly oriented CNs were homogeneously grown onto ACFs. The pre-immersion of cobalt(II ions for ACFs made the CNs grow above with a large pore size distribution, decreased the oxidation resistance, and exhibited different predominant N-functionalities after chemical vapor deposition processes. Specifically, the CNs grafted on ACFs with or without pre-immersion of cobalt(II ions were characterized by the pyridine-like structures of six-member rings or pyrrolic/amine moieties, respectively. In addition, the loss of microporosity on the specific surface area and pore volume exceeded the gain from the generation of the defects from CNs. The adsorption capacity of CO2 decreased gradually with increasing temperature, implying that CO2 adsorption was exothermic. The adsorption capacities of CO2 at 25 °C and 1 atm were between 1.53 and 1.92 mmol/g and the Freundlich equation fit the adsorption data well. The isosteric enthalpy of adsorption, implying physical adsorption, indicated that the growth of CNTs on the ACFs benefit CO2 adsorption.

Effect of l-lysine-assisted surface grafting for nano-hydroxyapatite on mechanical properties and in vitro bioactivity of poly(lactic acid-co-glycolic acid).

Science.gov (United States)

Liuyun, Jiang; Lixin, Jiang; Chengdong, Xiong; Lijuan, Xu; Ye, Li

2016-01-01

It is promising and challenging to study surface modification for nano-hydroxyapatite to improve the dispersion and enhance the mechanical properties and bioactivity of poly(lactic acid-co-glycolic acid). In this paper, we designed an effective new surface grafting with the assist of l-lysine for nano-hydroxyapatite, and the nano-hydroxyapatite surface grafted with the assist of l-lysine (g-nano-hydroxyapatite) was incorporated into poly(lactic acid-co-glycolic acid) to develop a series of g-nano-hydroxyapatite/poly(lactic acid-co-glycolic acid) nano-composites. The surface modification reaction for nano-hydroxyapatite, the mechanical properties, and in vitro human osteoblast-like cell (MG-63) response were characterized and investigated by Fourier transformation infrared, thermal gravimetric analysis, dispersion test, electromechanical universal tester, differential scanning calorimeter measurements, and in vitro cells culture experiment. The results showed that the grafting amount on the surface of nano-hydroxyapatite was enhanced with the increase of l-lysine, and the dispersion of nano-hydroxyapatite was improved more, so that it brought about better promotion crystallization and more excellent mechanical enhancement effect for poly(lactic acid-co-glycolic acid), comparing with the unmodified nano-hydroxyapatite. Moreover, the cells' attachment and proliferation results confirmed that the incorporation of the g-nano-hydroxyapatite into poly(lactic acid-co-glycolic acid) exhibited better biocompatibility than poly(lactic acid-co-glycolic acid). The above results indicated that the new surface grafting with the assist of l-lysine for nano-hydroxyapatite was an ideal novel surface modification method, which brought about better mechanical enhancement effect and in vitro bioactivity for poly(lactic acid-co-glycolic acid) with adding higher g-nano-hydroxyapatite content, suggesting it had a great potential to be used as bone fracture internal fixation materials

Study of PVDF/Graphene oxide nanocomposites by UV-Vis analysis

International Nuclear Information System (INIS)

Pereira, Juliana V.

2013-01-01

In this work we have prepared nanocomposites made by mixing Poly (vinylidene fluoride) [PVDF] and grapheme oxide nanosheets (GO) aiming to find dosimetric properties for applications in high dose dosimetry. Graphene Oxides (GO) nanosheets were synthesized by the Hummers method, using graphite supplied by Aldrich as the starting material. Nanocomposites were produced by mixing solved PDVF in DMAc with GO dispersed in an aqueous solution by sonication. The samples were irradiated with a Co-60 source at constant dose rate (12 kGy/h), with doses ranging from 50 to 1,000 kGy. The UV-Vis and spectrophotometry have been used to monitor the appearing of C=C conjugated bonds and radio-oxidation of carbon (C=O). The PVDF/OG nanocomposites prepared with 1.88 at.% of OG presented the best dosimetric properties. In this material, UVVis spectrometry has revealed that the absorbance intensities at 250 nm can be used for high dosimetry purposes for gamma doses ranging from 100 to 750 kGy. In this range, it is possible to observe a linear relationship between Abs and Dose. (author)

A super hydrophilic modification of poly(vinylidene fluoride) (PVDF) nanofibers: By in situ hydrothermal approach

Science.gov (United States)

Sheikh, Faheem A.; Zargar, Mohammad Afzal; Tamboli, Ashif H.; Kim, Hern

2016-11-01

Nanofibers fabricated from Poly(vinylidene fluoride) (PVDF) possesses potential applications in the field of filtrations, because of their excellent resistance towards harsh chemicals. However, the hydrophobicity restricts its further application. In this work, we focus on optimal parameters for post-electrospun tethering of Poly(vinyl alcohol) (PVA) as superhydrophilic domain onto each individual PVDF nanofibers by exploiting the in situ hydrothermal approach. The results indicated an increase in nanofiber diameters due to coating of PVA and improved surface wettability of PVDF nanofibers. The tensile tests of nanofibers indicated that mechanical properties of PVDF nanofibers could be sharply tuned from rigid to ductile. Furthermore, the studies strongly suggest that in situ hydrothermal treatment of post-electrospun nanofibers can improve the water contact angle and these nanofibers can be used in varied applications (e.g., in water purification systems).

PVDF-PZT nanocomposite film based self-charging power cell.

Science.gov (United States)

Zhang, Yan; Zhang, Yujing; Xue, Xinyu; Cui, Chunxiao; He, Bin; Nie, Yuxin; Deng, Ping; Lin Wang, Zhong

2014-03-14

A novel PVDF-PZT nanocomposite film has been proposed and used as a piezoseparator in self-charging power cells (SCPCs). The structure, composed of poly(vinylidene fluoride) (PVDF) and lead zirconate titanate (PZT), provides a high piezoelectric output, because PZT in this nanocomposite film can improve the piezopotential compared to the pure PVDF film. The SCPC based on this nanocomposite film can be efficiently charged up by the mechanical deformation in the absence of an external power source. The charge capacity of the PVDF-PZT nanocomposite film based SCPC in 240 s is ∼0.010 μA h, higher than that of a pure PVDF film based SCPC (∼0.004 μA h). This is the first demonstration of using PVDF-PZT nanocomposite film as a piezoseparator for SCPC, and is an important step for the practical applications of SCPC for harvesting and storing mechanical energy.

APPLICATION OF PIEZOELECTRIC MATERIAL FILM PVDF (Polyvinylidene Flouride AS LIQUID VISCOSITY SENSOR

Directory of Open Access Journals (Sweden)

Hananto F. S, Santoso D.R., Julius

2012-03-01

Research was done by taking 10 samples of oil and 3 different size ofPVDF film and a strain gage,that are: 1 cm x 3 cm (PVDF1; 1 cm x 2 cm (PVDF2; 1 cm x 1 cm (PVDF3. Results showed that the resolution of  PVDF1,  PVDF2 and PVDF3 are  4.6  mv/cPois;  3.1  mv/cPois and 1.5  mv/cPois respectively, while the strain gage produce a resolution of 1.2  mv/cPois. The average resolution of PVDF is 1.53 mv.cPois-1.cm-2, which means that every 1 cm2   PVDF film area and the increase of 1 cPois of viscosity of the material will produce 1.53 millivolts.

Hydrophobic Hyflon® AD/PVDF membranes for butanol dehydration via pervaporation

KAUST Repository

Jalal, Taghreed; Bettahalli Narasimha, Murthy Srivatsa; Le, Ngoc Lieu; Nunes, Suzana Pereira

2015-01-01

Novel hydrophobic Hyflon® AD /PVDF membranes were developed and investigated for n-butanol dehydration via pervaporation. The coating protocols for thin defect-free Hyflon® AD selective layer on the PVDF support was optimized. Water and n-butanol transport was measured, analyzing the effect of operating conditions. The water flux through the newly developed membranes was higher than 150 g/m2.h with selectivity for water higher than 99 wt %. The focus was on the use of Hyflon® AD as the selective layer for n-butanol dehydration. The membrane application can be extended to other solvents, supporting an effective and simple method for dehydration with hydrophobic membranes.

Hydrophobic Hyflon® AD/PVDF membranes for butanol dehydration via pervaporation

KAUST Repository

Jalal, Taghreed

2015-10-21

Novel hydrophobic Hyflon® AD /PVDF membranes were developed and investigated for n-butanol dehydration via pervaporation. The coating protocols for thin defect-free Hyflon® AD selective layer on the PVDF support was optimized. Water and n-butanol transport was measured, analyzing the effect of operating conditions. The water flux through the newly developed membranes was higher than 150 g/m2.h with selectivity for water higher than 99 wt %. The focus was on the use of Hyflon® AD as the selective layer for n-butanol dehydration. The membrane application can be extended to other solvents, supporting an effective and simple method for dehydration with hydrophobic membranes.

Surface grafting density analysis of high anti-clotting PU-Si-g-P(MPC) films

Energy Technology Data Exchange (ETDEWEB)

Lu Chunyan [Jiangsu Key Laboratory of Biofunctional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210097 (China); Jiangsu Engineering Research Center for Biomedical Function Materials, Nanjing Normal University, Nanjing 210097 (China); Zhou Ninglin, E-mail: ninglinzhou@yahoo.com [Jiangsu Key Laboratory of Biofunctional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210097 (China); Jiangsu Engineering Research Center for Biomedical Function Materials, Nanjing Normal University, Nanjing 210097 (China); Jiangsu Technological Research Center for Interfacial Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China); Xiao Yinghong; Tang Yida; Jin Suxing; Wu Yue [Jiangsu Key Laboratory of Biofunctional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210097 (China); Jiangsu Engineering Research Center for Biomedical Function Materials, Nanjing Normal University, Nanjing 210097 (China); Zhang Jun; Shen Jian [Jiangsu Key Laboratory of Biofunctional Materials, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210097 (China); Jiangsu Engineering Research Center for Biomedical Function Materials, Nanjing Normal University, Nanjing 210097 (China); Jiangsu Technological Research Center for Interfacial Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China)

2012-02-01

Well-defined zwitterionic polymer brushes with good blood compatibility were studied, grafted from polyurethane (PU) substrate (PU-Si-g-P(MPC)) by surface-initiated reverse atom transfer radical polymerization (SI-RATRP). We found that the structure of polymer brushes and hence their properties greatly depend on the grafting density. To solve the problems of the normal method for grafting density measurement, i.e., more requirements for qualified and proficient instrument operator, we established an effective and feasible way instead of the conventional method of spectroscopic ellipsometer combined with gel permeation chromatograph (ELM/GPC) to calculate the grafting density of PU-Si-g-P(MPC) films by using a software named ImageJ 1.44e in combination with scanning electronic microscope (SEM) or atomic microscope (AFM). X-ray photoelectron spectroscopy (XPS), SEM and AFM were employed to analyze the surface topography and changes of elements before and after graft modification of the synthetic PU-Si-g-P(MPC) biofilms.

Grafting poly ethylene glycol chains for antifouling purposes using supercritical CO2

DEFF Research Database (Denmark)

Lokanathan, Arcot R.

2011-01-01

solvent in processes involving PEG grafting for antifouling purposes. Significant chemical efficiency and extremely low surface tension makes scCO2 an apt solvent for Grafting PEG brushes into three dimensional micro or nano porous scaffolds related to tissue engineering. References: 1. Peter Kingshott...

Grafting of HEMA onto dopamine coated stainless steel by 60Co-γ irradiation method

International Nuclear Information System (INIS)

Jin, Wanqin; Yang, Liming; Yang, Wei; Chen, Bin; Chen, Jie

2014-01-01

A novel method for grafting of 2-hydroxyethyl methacrylate (HEMA) onto the surface of stainless steel (SS) was explored by using 60 Co-γ irradiation. The surface of SS was modified by coating of dopamine before radiation grafting. The grafting reaction was performed in a simultaneous irradiation condition. The chemical structures change of the surface before and after grafting was demonstrated by Fourier transform infrared (FTIR) spectrometer. The hydrophilicity of the samples was determined by water contact angle measurement in the comparison of the stainless steel in the conditions of pristine, dopamine coated and HEMA grafted. Surface morphology of the samples was characterized by atomic force microscope (AFM) and scanning electron microscope (SEM). The corrosion resistance properties of the samples were evaluated by Tafel polarization curve. The hemocompatibility of the samples were tested by platelet adhesion assay. - Highlights: • Poly-HEMA was grafted onto the surface of SS by 60 Co-γ-ray irradiation. • Pristine SS was coated by dopamine to form a dense poly-dopamine film before radiation grafting. • The biocompatibility and hydrophility of SS were improved after the grafting of HEMA

Enhanced dielectric and electrical properties of annealed PVDF thin film

Science.gov (United States)

Arshad, A. N.; Rozana, M. D.; Wahid, M. H. M.; Mahmood, M. K. A.; Sarip, M. N.; Habibah, Z.; Rusop, M.

2018-05-01

Poly (vinylideneflouride) (PVDF) thin films were annealed at various annealing temperatures ranging from 70°C to 170°C. This study demonstrates that PVDF thin films annealed at temperature of 70°C (AN70) showed significant enhancement in their dielectric constant (14) at frequency of 1 kHz in comparison to un-annealed PVDF (UN-PVDF), dielectric constant (10) at the same measured frequency. As the annealing temperature was increased from 90°C (AN90) to 150°C (AN150), the dielectric constant value of PVDF thin films was observed to decrease gradually to 11. AN70 also revealed low tangent loss (tan δ) value at similar frequency. With respect to its resistivity properties, the values were found to increase from 1.98×104 Ω.cm to 3.24×104 Ω.cm for AN70 and UN-PVDF films respectively. The improved in dielectric constant, with low tangent loss and high resistivity value suggests that 70°C is the favorable annealing temperature for PVDF thin films. Hence, AN70 is a promising film to be utilized for application in electronic devices such as low frequency capacitor.

Study of radiation grafted and sulfonated poly(tetrafluoroethylene-co-hexafluoropropylene), FEP, membranes

International Nuclear Information System (INIS)

Mohamed Mahmoud Nasef; Hamdani Saidi; Hussin Mohd Nor

1999-01-01

Radiation grafted and sulfonated FEP membranes were prepared by radiation-induced grafting of styrene onto poly(tetrafluoroethylene-co-hexafluoropropylene) films at room temperature and subsequently sulfonated. The membrane composition was controlled via variation of the grafting conditions such as type of diluent, irradiation dose, dose rate and monomer concentration. The membrane properties such as water uptake, ion exchange capacity and ionic conductivity were found to be strongly dependent upon the degree of grafting. The membranes were shown to have a good combination of physico-chemical properties, which made them promising for development of low cost proton exchange membranes

Absorbed dose/melting heat dependence studies for the PVDF homopolymer

International Nuclear Information System (INIS)

Batista, Adriana S.M.; Gual, Maritza R.; Pereira, Claubia

2013-01-01

Differential Scanning Calorimetry (DSC) of gamma irradiated Poly (vinylidene Fluoride) [PVDF] homopolymer has been studied in connection with the use of material in industrial high gamma dose measurement. Interaction between gamma radiation and PVDF leads to the radio-induction of C=O and conjugated C=C bonds, as it can be inferred from previous infrared (FTIR) and ultraviolet-visible (UV-Vis) spectrometric data. These induced defects result in a decrease of the polymer crystallinity that can be followed with DSC scans, by measuring the latent heat during the melting transition (Hmelt). After a systematic investigation, we have found that Hmelt is unambiguously related to the delivered doses ranging from 100 to 2,000 kGy of gamma radiation. One the other hand, further fading investigation analysis has proved that the Hmelt x Dose relationship can be fitted by an exponential function that remains constant for several months. Both the very large range of dose measurement and also the possibility of evaluating high gamma doses until five months after irradiation make PVDF homopolymers very good candidates to be investigated as commercial high gamma dose dosimeters. The high gamma dose irradiation facilities in Brazil used to develop high dose dosimeters are all devoted to industrial and medical purposes. Therefore, in view of the uncertainties involved in the dose measurements related to the electronic equilibrium correction factors and backscattering in the isodose curves used at the irradiation setup, a validation process is required to correctly evaluate the delivered absorbed doses. The sample irradiations were performed with a Co-60 source, at 12kGy/h and 2,592 kGy/h, in the high gamma dose facilities at Centro de Desenvolvimento da Tecnologia Nuclear CDTN/CNEN, Belo Horizonte, Brazil. The comparison of the curve of the Hmelt vs Dose is presented in this paper. (author)

Crystallization of calcium carbonate on radiation-grafted polyethylene films

International Nuclear Information System (INIS)

Hou Zhengchi; Zhang Fengying; Deng Bo; Yang Haijun; Chen Shuang; Sheng Kanglong

2006-01-01

In biomineralization processes, nucleation and growth of inorganic crystals can be regulated by organic template molecules. This has inspired great interest in studying mimic biomineralization. In our study, growing CaCO 3 crystals on PE films functionalized through radiation-induced grafting was attempted. PE films grafted with different functional groups of different distributions and densities were used as substrates for CaCO 3 nucleation and crystal growth from Ca(HCO 3 ) 2 supersaturated solution under different environmental conditions (e.g. additives and temperature) to study the effects and mechanisms. The grafted PE films were analyzed by ATR-FTIR and AFM, and the evolution of CaCO 3 crystal formation on the grafted PE film was characterized by SEM, FTIR, and XRD. The results indicated that heterogeneous nucleation of CaCO 3 crystals was significantly facilitated by the functional groups grafted on the surface of PE films, that the morphology of CaCO 3 crystals could be controlled by distribution and density of the grafted functional groups, and that polymorphism of CaCO 3 crystal could be regulated by selection of grafting functional groups. We believe that studying the effects of chemical structures on inorganic crystallization is of great importance since radiation-induced grafting is an effective method to graft desirable functional groups onto different polymers by selected monomers, in the endeavor of developing advanced organic/inorganic composites with high performance, with a wide availability of polymers, monomers and inorganic solutions. (authors)

Post irradiation effects on the graft of poly(tetrafluoroethylene-co-perfluoropropyl vinyl ether) (PFA) films

International Nuclear Information System (INIS)

Geraldes, Adriana N.; Zen, Heloisa A.; Ribeiro, Geise; Ferreira, Henrique P.; Souza, Camila P.; Parra, Duclerc F.; Lugao, Ademar B.

2009-01-01

Radiation induced grafting of monomers into fluorinated polymers was designed as an alternative route to polymer modification. In this work, grafting of styrene onto poly(tetrafluoroethylene-co-perfluoropropyl vinyl ether) (PFA) was studied. Radiation-induced grafting of styrene onto PFA films was investigated after simultaneous irradiation (in post-irradiation condition) using a 60 Co source. The films of PFA were irradiated at 20, 40, 80 and 100 kGy doses at room temperature and chemical changes were monitored after contact with styrene for grafting. The post-irradiation time was established between 7 and 28 days when films of PFA were maintained in styrene/toluene 1:1 v/v solution at room temperature. After these periods the grafting degrees were evaluated in the samples. The highest degree of grafting was achieved after 14 days. Chemical modifications were evaluated by infrared spectroscopic analysis (FTIR), thermogravimetry (TG), differential scanning calorimetry (DSC) and also by scanning electron microscopy (SEM). The degree of grafting (DOG) was determined gravimetrically. The results showed that irradiated PFA films at 100 kGy exhibited higher grafting degree. Surface analysis by SEM technique of irradiated, grafted and original films have presented an homogeneous surface. (author)

Optimization of reaction parameters of radiation induced grafting of 1-vinylimidazole onto poly(ethylene-co-tetraflouroethene) using response surface method

Energy Technology Data Exchange (ETDEWEB)

Nasef, Mohamed Mahmoud, E-mail: mahmoudeithar@fkkksa.utm.my [Institute of Hydrogen Economy, International Campus, Universiti Teknologi Malaysia, 54100 Kuala Lumpur (Malaysia); Aly, Amgad Ahmed; Saidi, Hamdani; Ahmad, Arshad [Institute of Hydrogen Economy, International Campus, Universiti Teknologi Malaysia, 54100 Kuala Lumpur (Malaysia)

2011-11-15

Radiation induced grafting of 1-vinylimidazole (1-VIm) onto poly(ethylene-co-tetraflouroethene) (ETFE) was investigated. The grafting parameters such as absorbed dose, monomer concentration, grafting time and temperature were optimized using response surface method (RSM). The Box-Behnken module available in the design expert software was used to investigate the effect of reaction conditions (independent parameters) varied in four levels on the degree of grafting (G%) (response parameter). The model yielded a polynomial equation that relates the linear, quadratic and interaction effects of the independent parameters to the response parameter. The analysis of variance (ANOVA) was used to evaluate the results of the model and detect the significant values for the independent parameters. The optimum parameters to achieve a maximum G% were found to be monomer concentration of 55 vol%, absorbed dose of 100 kGy, time in the range of 14-20 h and a temperature of 61 {sup o}C. Fourier transform infrared (FTIR), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to investigate the properties of the obtained films and provide evidence for grafting. - Highlights: > A precursor for phosphoric acid membrane for a high temperature PEM fuel cell was prepared. > The grafting parameters for radiation induced grafting of 1-VIm onto ETFE film were optimized. > Surface response method was used to predict the degree of grafting. > The predicted value agreed well with the experimental data as indicated by a 3% deviation. > The number of the experiments and cost of radiation induced grafting were reduced.

Efficient Preparation of Super Antifouling PVDF Ultrafiltration Membrane with One Step Fabricated Zwitterionic Surface.

Science.gov (United States)

Zhao, Xinzhen; He, Chunju

2015-08-19

On the basis of the excellent fouling resistance of zwitterionic materials, the super antifouling polyvinylidene fluoride (PVDF) membrane was efficiently prepared though one-step sulfonation of PVDF and polyaniline blend membrane in situ. The self-doped sulfonated polyaniline (SPANI) was generated as a novel zwitterionic polymer to improve the antifouling property of PVDF ultrafiltration membrane used in sewage treatment. Surface attenuated total reflection Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, surface zeta potential, and water contact angle demonstrated the successful fabrication of zwitterionic interface by convenient sulfonation modification. The static adsorption fouling test showed the quantified adsorption mass of bovine serum albumin (BSA) pollutant on the PVDF/SPANI membrane surface decreases to 3(±2) μg/cm(2), and the water flux recovery ratio (FRR) values were no less than 95% for the three model pollutants of BSA, sodium alginate (SA), and humic acid (HA), which were corresponding hydrophobic, hydrophilic, and natural pollutants in sewage, respectively. This Research Article demonstrated the antifouling advantages of zwitterionic SPANI and aimed to provide a simple method for the large scale preparation of zwitterionic antifouling ultrafiltration membranes.

Near DC force measurement using PVDF sensors

Science.gov (United States)

Ramanathan, Arun Kumar; Headings, Leon M.; Dapino, Marcelo J.

2018-03-01

There is a need for high-performance force sensors capable of operating at frequencies near DC while producing a minimal mass penalty. Example application areas include steering wheel sensors, powertrain torque sensors, robotic arms, and minimally invasive surgery. The beta crystallographic phase polyvinylidene fluoride (PVDF) films are suitable for this purpose owing to their large piezoelectric constant. Unlike conventional capacitive sensors, beta crystallographic phase PVDF films exhibit a broad linear range and can potentially be designed to operate without complex electronics or signal processing. A fundamental challenge that prevents the implementation of PVDF in certain high-performance applications is their inability to measure static signals, which results from their first-order electrical impedance. Charge readout algorithms have been implemented which address this issue only partially, as they often require integration of the output signal to obtain the applied force profile, resulting in signal drift and signal processing complexities. In this paper, we propose a straightforward real time drift compensation strategy that is applicable to high output impedance PVDF films. This strategy makes it possible to utilize long sample times with a minimal loss of accuracy; our measurements show that the static output remains within 5% of the original value during half-hour measurements. The sensitivity and full-scale range are shown to be determined by the feedback capacitance of the charge amplifier. A linear model of the PVDF sensor system is developed and validated against experimental measurements, along with benchmark tests against a commercial load cell.

Fabrication and evaluation of thin layer PVDF composites using MWCNT reinforcement: Mechanical, electrical and enhanced electromagnetic interference shielding properties

Directory of Open Access Journals (Sweden)

B. V. Bhaskara Rao

2016-06-01

Full Text Available Radar X-band electromagnetic interference shielding (EMS is one of the prime requirements for any air vehicle coating; with limitations on the balance between strength and thickness of the EMS material. Nanocomposite of multiwalled-carbon-nanotubes (MWCNT has been homogeneously integrated (0 – 9 wt% with polymer, poly (vinylidene fluoride, PVDF to yield 300 micron film. The PVDF + 9 wt% MWCNT sample of density 1.41 g/cm3 show specific shielding effectiveness (SSE of 17.7 dB/(g/cm3 (99.6% EMS, with maintained hardness and improved conductivity. With multilayer stacking (900 microns of these films of density 1.37 g/cm3, the sample showed increase in SSE to 23.3 dB/(g/cm3 (99.93% EMS. Uniform dispersion of MWCNTs in the PVDF matrix gives rise to increased conductivity in the sample beyond 5 wt% MWCNT reinforcement. The results are correlated to the hardness, reflection loss, absorption loss, percolation threshold, permittivity and the conductivity data. An extremely thin film with maximum EMS property is hence proposed.

Ag induced electromagnetic interference shielding of Ag-graphite/PVDF flexible nanocomposites thinfilms

Science.gov (United States)

Kumaran, R.; Alagar, M.; Dinesh Kumar, S.; Subramanian, V.; Dinakaran, K.

2015-09-01

We report Ag nanoparticle induced Electromagnetic Interference (EMI) shielding in a flexible composite films of Ag nanoparticles incorporated graphite/poly-vinylidene difluoride (PVDF). PVDF nanocomposite thin-films were synthesized by intercalating Ag in Graphite (GIC) followed by dispersing GIC in PVDF. The X-ray diffraction analysis and the high-resolution transmission electron microscope clearly dictate the microstructure of silver nanoparticles in graphite intercalated composite of PVDF matrix. The conductivity values of nanocomposites are increased upto 2.5 times when compared to neat PVDF having a value of 2.70 S/cm at 1 MHz. The presence of Ag broadly enhanced the dielectric constant and lowers the dielectric loss of PVDF matrix proportional to Ag content. The EMI shielding effectiveness of the composites is 29.1 dB at 12.4 GHz for the sample having 5 wt. % Ag and 10 wt. % graphite in PVDF.

Hydroquinone and Quinone-Grafted Porous Carbons for Highly Selective CO2 Capture from Flue Gases and Natural Gas Upgrading.

Science.gov (United States)

Wang, Jun; Krishna, Rajamani; Yang, Jiangfeng; Deng, Shuguang

2015-08-04

Hydroquinone and quinone functional groups were grafted onto a hierarchical porous carbon framework via the Friedel-Crafts reaction to develop more efficient adsorbents for the selective capture and removal of carbon dioxide from flue gases and natural gas. The oxygen-doped porous carbons were characterized with scanning electron microscopy, transmission electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, and Raman spectroscopy. CO2, CH4, and N2 adsorption isotherms were measured and correlated with the Langmuir model. An ideal adsorbed solution theory (IAST) selectivity for the CO2/N2 separation of 26.5 (298 K, 1 atm) was obtained on the hydroquinone-grafted carbon, which is 58.7% higher than that of the pristine porous carbon, and a CO2/CH4 selectivity value of 4.6 (298 K, 1 atm) was obtained on the quinone-grafted carbon (OAC-2), which represents a 28.4% improvement over the pristine porous carbon. The highest CO2 adsorption capacity on the oxygen-doped carbon adsorbents is 3.46 mmol g(-1) at 298 K and 1 atm. In addition, transient breakthrough simulations for CO2/CH4/N2 mixture separation were conducted to demonstrate the good separation performance of the oxygen-doped carbons in fixed bed adsorbers. Combining excellent adsorption separation properties and low heats of adsorption, the oxygen-doped carbons developed in this work appear to be very promising for flue gas treatment and natural gas upgrading.

Nanoclay embedded mixed matrix PVDF nanocomposite membrane: Preparation, characterization and biofouling resistance

International Nuclear Information System (INIS)

Rajabi, Hamid; Ghaemi, Negin; Madaeni, Sayed S.; Daraei, Parisa; Khadivi, Mohammad Ali; Falsafi, Monir

2014-01-01

Highlights: • Nanocomposite membranes were prepared by addition of OMMT to PVDF membrane. • Addition of nanoclay considerably increased the hydrophilicity of PVDF membrane. • Nanocomposite membranes had higher water flux and antifouling properties. • Fouling of membranes blended with nanoclay (<4 wt.%) reduced. - Abstract: In this paper, nanocomposite PVDF/nanoclay membranes were prepared with addition of different concentrations of organically modified montmorillonite (OMMT) into the polymeric casting solution using combination of solution dispersion and phase inversion methods. Membranes were characterized by use of X-ray diffraction (XRD), water contact angle, scanning electron microscopy (SEM) and atomic force microscopy (AFM), and their performances were evaluated in terms of pure water flux and fouling parameters. The surface hydrophilicity of all nanocomposites markedly improved compared to nascent PVDF. In addition, XRD patterns revealed the formation of intercalated layers of mineral clays in PVDF matrix. SEM and AFM images showed that addition of OMMT resulted in nanocomposite membranes with thinner skin layer and higher porosity rather than PVDF membranes. Pure water flux of PVDF/OMMT membranes increased significantly (particularly for fabricated membranes by 4 and 6 wt.% OMMT) compared to that of PVDF membrane. Moreover, nanocomposite membranes showed the elevated antifouling properties, and flux recovery of nascent PVDF membranes increased from 51 to 72% with addition of 2 wt.% OMMT nanoparticles. These nanocomposite membranes also offered a remarkable reusability and durability against biofouling

Nanoclay embedded mixed matrix PVDF nanocomposite membrane: Preparation, characterization and biofouling resistance

Energy Technology Data Exchange (ETDEWEB)

Rajabi, Hamid [Membrane Research Centre, Department of Chemical Engineering, Razi University, Tagh Bostan, 67149 Kermanshah (Iran, Islamic Republic of); Department of Civil Engineering, Razi University, 67149 Kermanshah (Iran, Islamic Republic of); Ghaemi, Negin, E-mail: negin_ghaemi@kut.ac.ir [Department of Chemical Engineering, Kermanshah University of Technology, 67178 Kermanshah (Iran, Islamic Republic of); Madaeni, Sayed S. [Membrane Research Centre, Department of Chemical Engineering, Razi University, Tagh Bostan, 67149 Kermanshah (Iran, Islamic Republic of); Daraei, Parisa [Department of Chemical Engineering, Kermanshah University of Technology, 67178 Kermanshah (Iran, Islamic Republic of); Khadivi, Mohammad Ali [Friedrich-Alexander University, Erlangen-Nuremberg, Egerland Strasse 3, D-91058 Erlangen (Germany); Falsafi, Monir [Department of Chemistry, Faculty of Science, Razi University, 67149 Kermanshah (Iran, Islamic Republic of)

2014-09-15

Highlights: • Nanocomposite membranes were prepared by addition of OMMT to PVDF membrane. • Addition of nanoclay considerably increased the hydrophilicity of PVDF membrane. • Nanocomposite membranes had higher water flux and antifouling properties. • Fouling of membranes blended with nanoclay (<4 wt.%) reduced. - Abstract: In this paper, nanocomposite PVDF/nanoclay membranes were prepared with addition of different concentrations of organically modified montmorillonite (OMMT) into the polymeric casting solution using combination of solution dispersion and phase inversion methods. Membranes were characterized by use of X-ray diffraction (XRD), water contact angle, scanning electron microscopy (SEM) and atomic force microscopy (AFM), and their performances were evaluated in terms of pure water flux and fouling parameters. The surface hydrophilicity of all nanocomposites markedly improved compared to nascent PVDF. In addition, XRD patterns revealed the formation of intercalated layers of mineral clays in PVDF matrix. SEM and AFM images showed that addition of OMMT resulted in nanocomposite membranes with thinner skin layer and higher porosity rather than PVDF membranes. Pure water flux of PVDF/OMMT membranes increased significantly (particularly for fabricated membranes by 4 and 6 wt.% OMMT) compared to that of PVDF membrane. Moreover, nanocomposite membranes showed the elevated antifouling properties, and flux recovery of nascent PVDF membranes increased from 51 to 72% with addition of 2 wt.% OMMT nanoparticles. These nanocomposite membranes also offered a remarkable reusability and durability against biofouling.

Graft Copolymerization Of Methyl Methacrylate Onto Agave Cellulose

International Nuclear Information System (INIS)

Noor Afizah Rosli; Ishak Ahmad; Ibrahim Abdullah; Farah Hannan Anuar

2014-01-01

The grafting polymerization of methyl methacrylate (MMA) and Agave cellulose was prepared and the grafting reaction conditions were optimized by varying the reaction time and temperature, and ratio of monomer to cellulose. The resulting graft copolymers were characterized by Fourier transform infrared, X-ray diffraction analysis, thermogravimetric analysis, and scanning electron microscopy (SEM). The experimental results showed that the optimal conditions were at a temperature of 45 degree Celsius for 90 min with ratio monomer to cellulose at 1:1 (g/ g). An additional peak at 1738 cm -1 which was attributed to the C=O of ester stretching vibration of poly(methyl methacrylate), appeared in the spectrum of grafted Agave cellulose. A slight decrease of crystallinity index upon grafting was found from 0.74 to 0.68 for cellulose and grafted cellulose, respectively. Grafting of MMA onto cellulose enhanced its thermal stability and SEM observation further furnished evidence of grafting MMA onto Agave cellulose with increasing cellulose diameter and surface roughness. (author)

Evaluation of ethanol aged PVDF: diffusion, crystallinity and dynamic mechanical thermal properties; Avaliacao do PVDF envelhecido em etanol combustivel: difusao, cristalinidade e propriedades termicas dinamico-mecanicas

Energy Technology Data Exchange (ETDEWEB)

Silva, Agmar J.J.; Costa, Marysilvia F., E-mail: agmar@metalmat.ufrj.br [Coordenacao dos Programas de Pos-Graduacao em Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil)

2015-07-01

This work discuss firstly the effect of the ethanol fuel absorption by PVDF at 60°C through mass variation tests. A Fickian character was observed for the ethanol absorption kinetics of the aged PVDF at 60°C. In the second step, the dynamic mechanical thermal properties (E’, E’, E” and tan δ) of the PVDF were evaluated through dynamic mechanical thermal analysis (DMTA). The chemical structure of the materials was analyzed by X-ray diffraction analysis (XRD), and significant changes in the degree of crystallinity were verified after the aging. However, DMTA results showed a reduction in the storage modulus (E') of the aged PVDF, which was associated to diffusion of ethanol and swelling of the PVDF, which generated a prevailing plasticizing effect and led to reduction of its structural stiffness. (author)

Fast and facile fabrication of antifouling and hemocompatible PVDF membrane tethered with amino-acid modified PEG film

Science.gov (United States)

Zhang, Shuyou; Cao, Jingjing; Ma, Na; You, Meng; Wang, Xushan; Meng, Jianqiang

2018-01-01

A fast and facile protocol is reported aiming at improving the antifouling property and hemocompatibility of poly(vinylidene fluoride) (PVDF) membranes by tethering PEG hydrogel and zwitterion immobilization. The coated PEG hydrogel was first prepared by interfacial polymerization and tethered on an alkali treated PVDF membrane (PVDFA) surface via a simultaneous thio-ene and thiol-epoxy reaction. Then, the thiol groups of cysteine reacted with the epoxy groups in PEG hydrogel to fabricate the PVDFA-g-Cys membrane. The membrane fabrication was complete within less than 20 min and was conducted in mild conditions. The successful preparation of PVDFA-g-Cys membrane was confirmed by ATR-FTIR and XPS. Raman spectroscopy showed that the hydrogels covalently bonded to the PVDF membrane surface. The membrane retained its mechanical strength after modification. The SEM measurements suggested that the membrane became denser after hydrogel coating, meanwhile, the EDX test verified that the functional species uniformly distributed in the membrane matrix. Water contact angle (WCA), protein adsorption and protein filtration tests showed significant improvements in hydrophilicity and antifouling properties for the modified membrane. The negativity of the membrane surface measured by the streaming potential method provides a basis for protein resistance and hemocompatibility. Moreover, the suppressed platelet adhesion and prolonged plasma coagulant time show that the PVDFA-g-Cys membrane has ultralow thrombotic potential and better hemocompatibility. The reported surface modification method combing thio-ene and thio-epoxy chemistry not only facilitates fabrication of hemocompatible PVDF membrane but also provide an universal chemical platform for multifunctionalization of porous membranes.

2. Sino-German workshop on fuel cells. Book of abstracts

Energy Technology Data Exchange (ETDEWEB)

NONE

2003-07-01

The CD-ROM contains the content of 13 lectures and 19 proposals for joint projects, which were presented on the second Sino-German Workshop on fuel cells. The topics of the 13 lectures are: Ab-initio calculations of oxygen species on low-index platinum surfaces (Pachenko, M.T.M. Koper, T.E. Shubina, S.J. Mitchell, E. Roduner). Cross-Linked (Composite) Polyaryl Blend Membranes for Membrane Fuel Cells. (J.A. Kerres, A. Ullrich, W. Zhang, M. Hein, V. Gogel, L. Joerissen, Th. Frey, A. Friedrich). Performance and Methanol Permeation of Direct Methanol Fuel Cells: Dependence on Operating Conditions and on Electrode Structure(V. Gogel, Th. Frey, K.A. Friedrich, L. Joerissen, J. Garche, Z. Yongsheng). Experimental Investigation of Flow Bed Configuration Effect on Performance of Liquid Feed Direct Methanol Fuel Cells. (H. Guo, C.F. Ma, M.H. Wang, F. Ye, J. Yu, Y. Wang, C.Y. Wang). Improvement of MEAs for DMFC by a tuned production sequence assisted by mathematical modelling (Lindermeir, G. Rosenthal, U. Kunz, U. Hoffmann). Performance of the self-breathing air DMFC with solution grafted PVDF-g-PSSA membranes (X. Qiu, G. Guo, W. Li, W. Zhu, L. Chen). Modeling the Effects of Methanol Crossover on DMFC (J. Zhang, Y. Wang). The characteristics of 40 kW PEM fuel cell engine for vehicle(M. Hou, P. Ming, H. Zhang). A New and Simple Method for Preparing Biocathode in Biofuel Cells (D. Sun, C. Cai, X. Li, W. Xing, T. Lu). Nonlinear Model Reduction of a Dynamic Two-dimensional Molten Carbonate Fuel Cell Model (M. Mangold, M. Sheng). Recent Advances in Design and Fabrication of Low-Temperature Solid Oxide Fuel Cells (C. Xia, G. Meng). Novel CVD Techniques for Micro- and IT-SOFC Fabrication (G. Meng, H. Song, Q. Dong, D. Peng). Fundamental properties of La{sub 0.6}Sr{sub 0.4}Co{sub 0.8}Fe{sub 0.2}O{sub 3-{delta}} at high temperatures (S. Wang, T.-L. Wen).

Lithium polyacrylate as a binder for tin-cobalt-carbon negative electrodes in lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Li Jing [Dept. of Chemistry, Dalhousie University, Halifax, N.S. B3H 3J5 (Canada); Le, D.-B. [3M Electronic Markets Materials Division, 3M Center, St. Paul, MN 55144-1000 (United States); Ferguson, P.P. [Dept. of Physics and Atmospheric Science, Dalhousie University, Halifax, N.S. B3H 3J5 (Canada); Dahn, J.R., E-mail: jeff.dahn@dal.c [Dept. of Chemistry, Dalhousie University, Halifax, N.S. B3H 3J5 (Canada); Dept. of Physics and Atmospheric Science, Dalhousie University, Halifax, N.S. B3H 3J5 (Canada)

2010-03-01

A lithium polyacrylate (Li-PAA) binder has been developed by 3M Company that is useful with electrodes comprising alloy anode materials. This binder was used to prepare electrodes made with Sn{sub 30}Co{sub 30}C{sub 40} material prepared by mechanical attrition. The electrochemical performance of electrodes using Li-PAA binder was characterized and compared to those using sodium carboxymethyl cellulose (CMC) and polyvinylidene fluoride (PVDF) binders. The Sn{sub 30}Co{sub 30}C{sub 40} electrodes using Li-PAA and CMC binders show much smaller irreversible capacity than the ones using PVDF binder. Poor capacity retention is observed when PVDF binder is used. By contrast, the electrodes using Li-PAA binder show excellent capacity retention for Sn{sub 30}Co{sub 30}C{sub 40} materials and a specific capacity of 450 mAh/g is achieved for at least 100 cycles. The results suggest that Li-PAA is a promising binder for electrodes made from large-volume change alloy materials.

Structural changes in PVDF fibers due to electrospinning and its effect on biological function

International Nuclear Information System (INIS)

Damaraju, Sita M; Wu, Siliang; Jaffe, Michael; Arinzeh, Treena Livingston

2013-01-01

Polyvinylidine fluoride (PVDF) is being investigated as a potential scaffold for bone tissue engineering because of its proven biocompatibility and piezoelectric property, wherein it can generate electrical activity when mechanically deformed. In this study, PVDF scaffolds were prepared by electrospinning using different voltages (12–30 kV), evaluated for the presence of the piezoelectric β-crystal phase and its effect on biological function. Electrospun PVDF was compared with unprocessed/raw PVDF, films and melt-spun fibers for the presence of the piezoelectric β-phase using differential scanning calorimetry, Fourier transform infrared spectroscopy and x-ray diffraction. The osteogenic differentiation of human mesenchymal stem cells (MSCs) was evaluated on scaffolds electrospun at 12 and 25 kV (PVDF-12 kV and PVDF-25 kV, respectively) and compared to tissue culture polystyrene (TCP). Electrospinning PVDF resulted in the formation of the piezoelectric β-phase with the highest β-phase fraction of 72% for electrospun PVDF at 25 kV. MSCs cultured on both the scaffolds were well attached as indicated by a spread morphology. Cells on PVDF-25 kV scaffolds had the greatest alkaline phosphatase activity and early mineralization by day 10 as compared to TCP and PVDF-12 kV. The results demonstrate the potential for the use of PVDF scaffolds for bone tissue engineering applications. (paper)

Chemical modification of carbon powders with aminophenyl and aryl-aliphatic amine groups by reduction of in situ generated diazonium cations: Applicability of the grafted powder towards CO{sub 2} capture

Energy Technology Data Exchange (ETDEWEB)

Aurelie Grondein; Daniel Belanger [Universite du Quebec a Montreal, Montreal, PQ (Canada). Departement de Chimie

2011-08-15

Aminophenyl, p-aminobenzyl and p-aminoethylphenyl groups were grafted at the surface of carbon Vulcan XC72R by spontaneous reduction of the in situ generated diazonium cations from the corresponding amine. X-ray photoelectron spectroscopy and elemental analysis confirmed an amine loading of about 1 mmol/g. The grafting of amine functionalities leads to a decrease of specific surface area from 223 to about 110 m{sup 2}/g with a drastic loss of microporosity. Acid-base properties of the surface are also affected by the modification. Aminophenyl grafted groups make the surface more acidic while aryl-aliphatic amines groups tends to render it more basic. The grafted layer shows in each case a good thermal stability up to 250{sup o}C. The affinity of the modified powder towards CO{sub 2} and N{sub 2} has been evaluated by thermal swing adsorption. The maximum adsorption capacity of CO{sub 2} of modified carbons is lower than the unmodified carbon but the presence of the amine functionalities involves a better selectivity of the material towards CO{sub 2} adsorption in comparison of N{sub 2} adsorption. 53 refs., 9 figs., 3 tabs.

Synthesis and characterization of oil palm empty fruit bunch-grafted-polyvinyl alcohol (OPEFB-g-PVA) hydrogel for removal of copper ions from aqueous solution

Science.gov (United States)

Wen, Soh Jing; Rabat, Nurul Ekmi; Osman, Noridah

2017-12-01

Oil palm empty fruit bunch (OPEFB) fiber is a natural polymer which is potentially used as efficient adsorbents for heavy metal cations. The main objective of this research is to synthesize OPEFB grafted polyvinyl alcohol (PVA) hydrogel by using ammonium persulfate (APS) as initiator and gelatin as crosslinking agent. The grafting temperature, amounts of cross linking agent, initiator and concentration of OPEFB were manipulated in order to optimize the swelling capability of the hydrogel. Comparison of heavy metal adsorption performance between pure PVA hydrogel and optimized OPEFB-g-PVA hydrogel was evaluated by using copper ions solution. The characteristics and structure of the optimized OPEFB-g-PVA hydrogel was studied by using Fourier Transform Infrared (FTIR) spectroscopy and Scanning Electron Microscopy (SEM) while Thermogravimetric Analysis (TGA) was used to study its thermal stability. The presence of band at 1088 and 1047cm-1 corresponds to C-O was observed as strong evidence of grafting. Water uptake capacity was evaluated and the maximum water absorption capacity was obtained at 180.67 g/g. PVA hydrogel with OPEFB proved to have better copper ion absorbency and thermal properties compared to pure PVA hydrogel.

Modification of polyethersulfone films by grafting hydrophilic monomers with 60Co γ-rays

International Nuclear Information System (INIS)

Hou Zhengchi; Deng Bo; Li Jing

2006-01-01

Polyethersulfone (PES), with its high strength, high temperature resistance, corrosion- resistance, oxidation resistance and applicability under wide pH range, is used extensively as ultrafiltration and nanofiltration membrane. However, PES membranes foul easily in such an application because of hydrophobic nature of PES raw materials. Improving the hydrophilicity of PES by grafting hydrophilic monomers onto it is of potential to solve the problem. At present, common approaches to improve hydrophilicity of PES membranes are UV grafting modification, plasma modification, and chemical modification, whereas grafting and modifying PES films by 60 Co γ-rays has rarely been reported. Studies have been carried out in our laboratory to graft hydrophilic monomers onto PES membranes directly or PES powders via simultaneous radiation grafting with the rays. Acrylic acid, methyl acrylic acid or acrylamide was used to study effects of the monomer concentration, irradiation dose and dose rate, solvent, inhibitor and pH of the grafting solution on the degree of grafting. The results showed that hydrophilicity of all the PES membranes could be improved, with the extent of improvement being dependent on the grafting conditions. (authors)

Caraterização composicional do AES - um copolímero de enxertia de poli(estireno-co-acrilonitrila em poli(etileno-co-propileno-co-dieno Compositional characterization of AES a graft copolymer based on poly(styrene-co-acrylonitrile and poly(etyhlene-co-propylene-co-diene

Directory of Open Access Journals (Sweden)

Renato Turchet

2006-06-01

Full Text Available O objetivo deste trabalho é a caracterização do AES, um copolímero de enxertia de poli(estireno-co-acrilonitrila, SAN, em poli(etileno-co-propileno-co-dieno, EPDM. Para tanto, o AES foi submetido à extração seletiva de seus componentes: o SAN livre, o EDPM livre, e o copolímero de enxertia EPDM-g-SAN. O AES e suas frações foram caracterizados por espectroscopia de infravermelho, análise elementar, calorimetria diferencial de varredura e ressonância magnética nuclear, RMN¹H e RMN13C. O AES analisado apresenta a seguinte composição em massa: 65% de EPDM-g-SAN, 13% de EPDM livre e 22% de SAN livre. O EPDM apresenta 69,8% em massa de etileno, 26,5% em massa de propileno e 4,6% em massa do dieno, 2-etilideno-5-norboneno, ENB. O SAN apresenta razão em massa acrilonitrila/estireno de 28/72 e distribuição randômica de comonômeros de estireno e acrilonitrila. Estes resultados são concordantes com a composição do AES fornecida pelo fabricante, indicando que a metodologia proposta é adequada.This work aims the characterization of AES, a graft copolymer based on poly(styrene-co-acrylonitrile, SAN, and poly(etyhlene-co-propylene-co-diene, EPDM. AES was submitted to selective extraction of its components: free SAN, EPDM chains and the graft copolymer EPDM-g-SAN. AES and its fractions were characterized by infrared spectroscopy, elemental analysis, differential scanning calorimetry, 13C and ¹H nuclear magnetic resonance. The AES has 65 wt % of EPDM-g-SAN, 13 wt % of free EPDM and 22 wt % of free SAN. EPDM has 69.8 wt % of ethylene, 26.5 wt % of propylene and 4.6 wt % of diene, 2-ethylidene-5-norbonene ENB. SAN presents acrylonitrile/styrene mass ratio of 28/72 and a random distribution of acrylonitrile and styrene comonomers. These results are in agreement with the composition reported by the AES supplier, indicating that the proposed methodology is adequate.

Improvement of antifouling performances for modified PVDF ultrafiltration membrane with hydrophilic cellulose nanocrystal

Science.gov (United States)

Lv, Jinling; Zhang, Guoquan; Zhang, Hanmin; Zhao, Chuanqi; Yang, Fenglin

2018-05-01

Hydrophilic cellulose nanocrystal (CNC) was incorporated into hydrophobic poly(vinylidene fluoride) (PVDF) membrane via phase inversion process to improve membrane antifouling property. The effects of CNC on membrane morphology, hydrophilicity, permeability and antifouling property were investigated in-detail. Results indicated that the introduction of CNC into PVDF membrane enhanced the permeability by optimizing membrane microstructure and improving membrane hydrophilicity. A higher pure water flux of 206.9 L m-2 h-1 was achieved for CNC/PVDF membrane at 100 kPa, which was 20 times that of PVDF membrane (9.8 L m-2 h-1). In bovine serum albumin filtration measurements, the permeation flux and flux recovery ratio of CNC/PVDF membrane were increased remarkably, while the irreversible fouling-resistance of CNC/PVDF membrane decreased by 48.8%. These results indicated that the CNC/PVDF membrane possessed superior antifouling property due to the hydrophilicity of CNC that formed a hydration layer on the membrane surface to effectively reduce contaminants adsorption/deposition.

Conservation of the piezoelectric response of PVDF films under irradiation

Science.gov (United States)

Melilli, G.; Lairez, D.; Gorse, D.; Garcia-Caurel, E.; Peinado, A.; Cavani, O.; Boizot, B.; Clochard, M.-C.

2018-01-01

As opposed to piezo-ceramics (i.e PZT), flexibility and robustness characterize piezoelectric polymers. The main advantage of a piezoelectric polymer, such as Poly (vinylidene fluoride) (PVDF), is an electric power generation under large reversible elastic deformation. Starting from polarized PVDF, we have shown that, despite the fact that irradiation is known to structurally modify the PVDF by introducing defects (radicals, chain scission and crosslinks), the electro-active properties were not affected. At doses lower than 100 kGy, a comparison between swift heavy-ion (SHI) and e-beam irradiations is presented. A homemade device was realized to measure the output voltage as a function of the bending deformation for irradiated and non-irradiated PVDF film. DSC and FT-IR techniques give new insights on which crystalline part or structural change contributes to the conservation of the output voltage. Results suggest that despite the material after irradiation is composed of smaller crystallites, the β-phase content remains stable around 36%, which explains the remarkable preservation of the piezoelectric response in irradiated polarized PVDF films.

Study of properties of Pvdf aged and non aged in petroleum; Estudo das propriedades de PVDF envelhecido e nao envelhecido em petroleo

Energy Technology Data Exchange (ETDEWEB)

Oliveira, G.L.; Costa, M.F. [Coordenacao dos Programas de Pos-Graduacao de Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia Metalurgica e de Materiais], e-mail: geovaniolo@metalmat.ufrj.br

2010-07-01

The use polymer materials in complex structure such as flexible risers to offshore application is increasingly on the rise. One the materials used in these structures is poly(vinylidene fluoride) (PVDF). Attentive to the challenges found in the environments in which these structures are employed, PVDF copolymer samples were prepared by compression molding. After, materials were aged in petroleum at 80 deg C to assess effect of fluid in polymer. Characterization of samples was carried out by infrared spectroscopy (FTIR), X-ray diffraction (XRD) and tensile stress according to ASTM D 638. Instrumented indentation testing applying Vickers indenter was used to assess the effect of petroleum in PVDF. (author)

Effect of gamma rays on grafting parameters and liquid retention property of cassava starch-g-PAN

International Nuclear Information System (INIS)

Kiatkamjornwong, S.; Chvajarernpun, J.; Nakason, C.

1992-01-01

Radiation modification on liquid retention properties of native cassava starch, gelatinized at 85 0 C, by graft copolymerization with acrylonitrile was carried out by mutual irradiation to γ-rays. A thin aluminium foil was used to cover the inner wall of the reaction vessel so that the extent of homo polymer could be reduced to be less than 1.6% with a distilled water retention value of 665 g/g of the dry weight of the saponified grafted product. Confirmations of graft copolymerization and saponification reactions were made by the infrared spectrophotometric technique. The combined effect of radiation parameters in terms of an irradiation time and a dose rate to the same total dose on the extent of grafting reaction expressed in terms of grafting parameters which directly influenced liquid retention values was evaluated in conjunction with statistical analysis

Improved flexoelectricity in PVDF/barium strontium titanate (BST) nanocomposites

Science.gov (United States)

Hu, Xinping; Zhou, Yang; Liu, Jie; Chu, Baojin

2018-04-01

The flexoelectric effect of polymers is normally much weaker than that of ferroelectric oxides. In order to improve the flexoelectric response of the poly(vinylidene fluoride) (PVDF) ferroelectric polymer, PVDF/Ba0.67Si0.33TiO3 (BST) nanocomposites were fabricated. BST nanofibers were prepared by the electrospinning method, and the fibers were further surface modified with H2O2 to achieve a stronger interfacial interaction between the fibers and polymer matrix. Due to the high dielectric properties and strong flexoelectric effect of the BST, both dielectric constant and flexoelectric response of the composite with 25 vol. % surface modified BST are 3-4 times higher than those of PVDF. The dependence of the dielectric constant and the flexoelectric coefficient on the composition of the nanocomposites can be fitted by the empirical Yamada model, and the dielectric constant and the flexoelectric coefficient are correlated by a linear relationship. This study provides an approach to enhance the flexoelectric response of PVDF-based polymers.

Study polymeric membranes PVDF/TiO2 photocatalytic applications with synthesized by solution blow spinning

International Nuclear Information System (INIS)

Gimenes, T.C.; Pereira, E.A.; Montanhera, M.A.; Paula, F.R. de; Spada, E.R.

2016-01-01

In this study we obtained nanofibers titanium dioxide (TiO2) incorporated into the poly (vinylidene fluoride) - PVDF in different concentrations, using a new technique denominated Solution Blow Spinning. This technique has the merits of simplicity, low cost and high efficiency in the production of nanofibers, compared with the technique of Electrospinning, using pressurized gas instead of high voltage, is not limited to the dielectric constant of the material and provides a processing period of at least 100 times faster. The obtained nanofibers exhibit little account and a very smooth morphology, with diameters ranging from 400 to 700 nm and with presence of crystalline anatase phase. The tests showed photocatalytic degradation of Rhodamine B dye, being more degradation shown by the PVDF nanofibers containing 0,7 g of TiO 2 , approximately 75 % of degraded dye. However nanofibers obtained the PVDF/TiO2 applications of this material are numerous, as filters, conductive nanofibers, photocatalysis and sensors. (author)

Preparation of the copolymer of acrylic acid and acrylamide grafted onto polyethylene and its complexation with samarium ion

International Nuclear Information System (INIS)

Kido, Junji; Akiba, Hideto; Nishide, Hiroyuki; Tsuchida, Eishun; Omichi, Hideki; Okamoto, Jiro.

1986-01-01

Acrylic acid (AA) and acrylamide (AAm) were graft-copolymerized onto polyethylene (PE) powder by the pre-irradiation method. Complex formation constants of Sm ion with the PE powder grafted with both AA and AAm (PE-g-(AA-co-AAm)) were larger than those with the PE powder grafted with AA (PE-g-AA). Sm ion was efficiently separated from the solution containing both Sm ion and a transition metal ion such as Cu ion. Even after the γ-ray irradiation on PE-g-(AA-co-AAm) and PE-g-AA, the adsorption did not decrease. (author)

Evaluation of ethanol aged PVDF: diffusion, crystallinity and dynamic mechanical thermal properties

International Nuclear Information System (INIS)

Silva, Agmar J.J.; Costa, Marysilvia F.

2015-01-01

This work discuss firstly the effect of the ethanol fuel absorption by PVDF at 60°C through mass variation tests. A Fickian character was observed for the ethanol absorption kinetics of the aged PVDF at 60°C. In the second step, the dynamic mechanical thermal properties (E’, E’, E” and tan δ) of the PVDF were evaluated through dynamic mechanical thermal analysis (DMTA). The chemical structure of the materials was analyzed by X-ray diffraction analysis (XRD), and significant changes in the degree of crystallinity were verified after the aging. However, DMTA results showed a reduction in the storage modulus (E') of the aged PVDF, which was associated to diffusion of ethanol and swelling of the PVDF, which generated a prevailing plasticizing effect and led to reduction of its structural stiffness. (author)

CO{sub 2} adsorption in amine-grafted zeolite 13X

Energy Technology Data Exchange (ETDEWEB)

Bezerra, Diôgo P. [GPSA, Universidade Federal do Ceará (Brazil); Instituto Federal de Educação, Ciência e Tecnologia do Rio Grande do Norte, Campus Ipanguaçu, Rio Grande do Norte (Brazil); Silva, Francisco W.M. da; Moura, Pedro A.S. de; Sousa, Allyson G.S.; Vieira, Rodrigo S. [GPSA, Universidade Federal do Ceará (Brazil); Rodriguez-Castellon, Enrique [Departamento de Química Inorgánica, Facultad de Ciencias, Universidad de Málaga, 29071 Málaga (Spain); Azevedo, Diana C.S., E-mail: diana@gpsa.ufc.br [GPSA, Universidade Federal do Ceará (Brazil)

2014-09-30

Highlights: • CO{sub 2} adsorption mechanism in amine-grafted zeolite 13X was investigated. • The loaded amine tends to fill zeolite micropores and most of it is unaccessible to react with CO{sub 2}. • Part of loaded MEA binds covalently to the zeolitic structure and will not detach from the surface even at low pressures. • Chemisorption is likely to lead to CO{sub 2} higher uptakes upon a rise in temperature for solids with the highest amine load. - Abstract: The adsorption of CO{sub 2} on Zeolite 13X functionalized with amino groups was studied. Adsorbent functionalization was carried out by grafting with different loads of monoethanolamine (MEA). The adsorbents were characterized by N{sub 2} adsorption/desorption isotherms at 77 K, x-ray diffraction, TGA, in situ FTIR, XPS and adsorption microcalorimetry. CO{sub 2} isotherms were studied in a gravimetric device up to 10 bar at 298 and 348 K. It was found that increasing loads of amine to the adsorbent tend to reduce micropore volume of the resulting adsorbents by pore blocking with MEA. There is experimental evidence that part of the loaded MEA is effectively covalently bonded to the zeolitic structure, whereas there is also physisorbed excess MEA which will eventually be desorbed by raising the temperature beyond MEA boiling point. Heats of adsorption at nearly zero coverage indicate that some of the adsorbed CO{sub 2} reacts with available amino groups, which agrees with the finding that the adsorption capacity increases with increasing temperature for the modified zeolite with the highest MEA load.

Optimization strategies for radiation induced grafting of 4-vinylpyridine onto poly(ethylene-co-tetraflouroethene) film using Box–Behnken design

International Nuclear Information System (INIS)

Mahmoud Nasef, Mohamed; Shamsaei, Ezzatollah; Ghassemi, Payman; Ahmed Aly, Amgad; Hamid Yahaya, Abdul

2012-01-01

The radiation induced grafting of 4-vinylpyridine (4-VP) onto poly(ethylene-co-tetrafluoroethene) (ETFE) was optimized using the Box–Behnken factorial design available in the response surface method (RSM). The optimized grafting parameters; absorbed dose, monomer concentration, grafting time and reaction temperature were varied in four levels to quantify their effect on the grafting yield (GY). The validity of the statistical model was supported by the small deviation between the predicted (GY=61%) and experimental (GY=57%) values. The optimum conditions for enhancing GY were determined at the following values: monomer concentration of 48 vol%, absorbed dose of 64 kGy, reaction time of 4 h and temperature of 68 °C. A comparison was made between the optimization model developed for the present grafting system and that for grafting of 1-vinylimidazole (1-VIm) onto ETFE to confirm the validly and reliability of the Box–Behnken for the optimization of various radiation induced grafting reactions. Fourier transform infrared (FTIR), thermogravimetric analysis (TGA) and X-ray diffraction (XRD) were used to investigate the properties of the obtained films and provide evidence for grafting. - Highlights: ► Radiation induced grafting of 4-VP onto ETFE was studied in comparison of that of VIm onto ETFE. ► The parameters of grafting reaction were optimized using Box–Behnken factorial design. ► A statistical model to predict G% was developed taking the nature of 4-VP into account. ► The predicted response value agreed well with the experimental data as indicated by a 4% deviation. ► The model proved to be valid and reliable tool for predicting various radiation grafting reactions.

Flux and Passage Enhancement in Hemodialysis by Incorporating Compound Additive into PVDF Polymer Matrix

Directory of Open Access Journals (Sweden)

Qinglei Zhang

2016-10-01

Full Text Available In this study, Polyvinylidene fluoride (PVDF hollow fiber hemodialysis membranes were prepared by non-solvent induced phase separation (NIPS with compound addtive. The compound additive was made with polyvinyl pyrrolidone (PVP and Poly ethylene glycol (PEG. The results showed that the modified PVDF membrane had better separation performance than virgin PVDF membrane. The UF flux of modified PVDF membrane can reach 684 L·h−1·m−2 and lysozyme (LZM passage is 72.6% while virgin PVDF membrane is 313 L·h−1·m−2 and 53.2%. At the same time, the biocompatibility of PVDF membranes was also improved. Compared with commercial polysulfone hemodialysis membrane (Fresenius F60S membrane, the modified PVDF membrane had better mechanical and separation performance. The stress and tensile elongation of modified PVDF membrane was 0.94 MPa and 352% while Fresenius F60S membrane was 0.79 MPa and 59%. The LZM passage reached 72.6% while Fresenius F60S membrane was 54.4%. It was proven that the modified PVDF membrane showed better hydrophilicity, antithrombogenicity, less BSA adsorption, and lower hemolytic ratio and adhesion of platelets. Water contact angle and BSA adsorption of the modified PVDF membrane are 38° and 45 mg/m2 while Fresenius F60S membrane are 64° and 235 mg/m2. Prothrombin time (PT and activated partial thromboplastin time (APTT of the modified PVDF membrane are 56.5 s and 25.8 s while Fresenius F60S membrane is 35.7 s and 16.6 s. However, further biocompatibility evaluation is needed to obtain a more comprehensive conclusion.

Preparation of grafted microspheres CPVA-g-PSSS and studies on their drug-carrying and colon-specific drug delivery properties

International Nuclear Information System (INIS)

Gao, Baojiao; Fang, Li; Men, Jiying; Zhang, Yanyan

2013-01-01

Sodium 4-styrene sulfonate (SSS) was graft-polymerized on the surfaces of crosslinked polyvinyl alcohol (CPVA) microspheres in a manner of surface-initiated graft-polymerization by using cerium salt-hydroxyl group redox initiation system, obtaining the grafted microspheres CPVA-g-PSSS. The chemical structure and physicochemical characters of CPVA-g-PSSS microspheres were fully characterized with infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and zeta potential determination. The aim of this work is to constitute a novel colon-specific drug delivery system via molecular design by using CPVA-g-PSSS microspheres as the drug-carrying material and by taking metronidazole (MTZ) as the model drug. The drug-carrying ability and mechanism of the grafted microspheres CPVA-g-PSSS for MTZ were investigated. Finally, in-vitro release tests for the drug-carrying microspheres were conducted. The experimental results show that in an acidic medium, the grafted microspheres CPVA-g-PSSS exhibit strong adsorption ability for MTZ by driving of electrostatic interaction, and have an adsorption capacity of 112 mg/g, displaying the high efficiency of drug-carrying. The in-vitro release behavior of the drug-carried microspheres is highly pH-sensitive. In the medium of pH = 1, the drug-carrying microspheres do not release the drug, whereas in the medium of pH = 7.4, a sudden delivery phenomenon of the drug will occur, displaying an excellent colon-specific drug delivery behavior. Highlights: ► A metronidazole colon-specific drug delivery was constituted using grafted polymeric microspheres. ► Grafted polymeric microspheres CPVA-g-PSSS were prepared via surface-initiated graft-polymerization. ► The release of the drug-carrying microspheres is highly pH-sensitive. ► The drug-carrying microspheres display an excellent colon-specific drug delivery behavior

Preparation of grafted microspheres CPVA-g-PSSS and studies on their drug-carrying and colon-specific drug delivery properties

Energy Technology Data Exchange (ETDEWEB)

Gao, Baojiao, E-mail: gaobaojiao@126.com [Department of Chemical Engineering, North University of China, Taiyuan 030051, People' s Republic of China (China); Fang, Li [School of Chemistry and Chemical engineering, Shanxi University, Taiyuan 030006 (China); Men, Jiying; Zhang, Yanyan [Department of Chemical Engineering, North University of China, Taiyuan 030051, People' s Republic of China (China)

2013-04-01

Sodium 4-styrene sulfonate (SSS) was graft-polymerized on the surfaces of crosslinked polyvinyl alcohol (CPVA) microspheres in a manner of surface-initiated graft-polymerization by using cerium salt-hydroxyl group redox initiation system, obtaining the grafted microspheres CPVA-g-PSSS. The chemical structure and physicochemical characters of CPVA-g-PSSS microspheres were fully characterized with infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and zeta potential determination. The aim of this work is to constitute a novel colon-specific drug delivery system via molecular design by using CPVA-g-PSSS microspheres as the drug-carrying material and by taking metronidazole (MTZ) as the model drug. The drug-carrying ability and mechanism of the grafted microspheres CPVA-g-PSSS for MTZ were investigated. Finally, in-vitro release tests for the drug-carrying microspheres were conducted. The experimental results show that in an acidic medium, the grafted microspheres CPVA-g-PSSS exhibit strong adsorption ability for MTZ by driving of electrostatic interaction, and have an adsorption capacity of 112 mg/g, displaying the high efficiency of drug-carrying. The in-vitro release behavior of the drug-carried microspheres is highly pH-sensitive. In the medium of pH = 1, the drug-carrying microspheres do not release the drug, whereas in the medium of pH = 7.4, a sudden delivery phenomenon of the drug will occur, displaying an excellent colon-specific drug delivery behavior. Highlights: ► A metronidazole colon-specific drug delivery was constituted using grafted polymeric microspheres. ► Grafted polymeric microspheres CPVA-g-PSSS were prepared via surface-initiated graft-polymerization. ► The release of the drug-carrying microspheres is highly pH-sensitive. ► The drug-carrying microspheres display an excellent colon-specific drug delivery behavior.

Fabrication of beta-PVDF membranes by track etching and specific functionalization of nano-pores

International Nuclear Information System (INIS)

Cuscito, O.

2008-01-01

Poly(vinylidene fluoride)(β-PVDF) nano-porous membranes were made by chemical revealing of tracks induced from swift heavy ions irradiation. Pore opening and radii can be varied in a controllable manner with the etching time. nano-pores size in nano-meter scale (from 12 nm to 50 nm) appears to be linearly dependent to the etching time. It was then necessary to adapt the characterization tools to these membranes. Consequently, we resorted to the use of structural analysis methods (Scanning Electron Microscopy, Small Angle Neutron Scattering) and developed evaluation methods of the membranes transport properties like gas permeation and ionic diffusion. Results obtained confirm the pores opening (break through) and the hydrophobicity of material, which we have modified with hydrophilic molecules. In this precise case, the grafting of acrylic acid was initiated by the radicals still remains after track-etching (called radio-grafting). This key result was obtained by a study of Electron Paramagnetic Resonance. The labelling of introduced chemical functionalities with fluorescent probes was a very effective mean to visualize very few amounts of molecules by confocal microscopy. The radio-grafting was found specifically localized inside etched tracks. The protocol offers the possibility to create a double functionality, the one localized inside the nano-pores and the other on the surface of membranes. The modification of radio-grafting parameters (the acrylic acid concentration, solvent nature, use of transfer agent) and the chemical properties of the nano-pore walls have a direct incidence on the transport properties. (author) [fr

Investigation of the physico-mechanical properties of electrospun PVDF/cellulose nanofibers.

OpenAIRE

Issa, A.A.; Al-Maadeed, M.; Luyt, A.S.; Mrlik, M.; Hassan, M.K.

2016-01-01

The electro-activity and mechanical properties of PVDF depends mainly on the b-phase content and degree of crystallinity. In this study, cellulose fibers were used to improve these characteristics. This could be achieved because the hydroxyl groups on cellulose would force the fluorine atoms in PVDF to be in the trans-conformation, and the cellulose particles could act as nucleation centers. Electrospinning was used to prepare the PVDF/cellulose (nano)fibrous films, and this improved the tota...

Sulfonate-grafted porous polymer networks for preferential CO(2) adsorption at low pressure

NARCIS (Netherlands)

Lu, W.; Yuan, D.; Sculley, J.; Zhao, D.; Krishna, R.; Zhou, H.-C.

2011-01-01

A porous polymer network (PPN) grafted with sulfonic acid (PPN-6-SO3H) and its lithium salt (PPN-6-SO3Li) exhibit significant increases in isosteric heats of CO2 adsorption and CO2-uptake capacities. IAST calculations using single-component-isotherm data and a 15/85 CO2/N2 ratio at 295 K and 1 bar

Functionalized Nanoporous Track Etched {beta}-PVDF Membrane Electrodes for Lead (II) Determination by Square Wave Anodic Stripping Voltammetry

Energy Technology Data Exchange (ETDEWEB)

Bessbousse, H [Laboratoire des Solides Irradies, CEA-CNRS-Ecole Polytechnique, 91128 Palaiseau (France); Nadhakumar, I [School of Chemistry, University of Southampton, University Road, Southampton S017 1BJ (United Kingdom); Decker, M; Clochard, M -C; Wade, T L [Laboratoire des Solides Irradies, CEA-CNRS-Ecole Polytechnique, 91128 Palaiseau (France); Barsbay, M [Hacettepe University, Department of Chemistry, Polymer Chemistry Division, 06800 Beytepe Ankara (Turkey)

2012-09-15

Track etched functionalized nanoporous {beta}-PVDF membrane electrodes, or functionalized membrane electrodes (FME), are thin-layer cells made from poly(acrylic acid) (PAA) functionalized nanoporous {beta}-poly(vinylidene fluoride) ({beta}-PVDF) membranes with thin Au films sputtered on each side as electrodes. The Au film is thin enough that the pores of the membranes are not completely covered. The PAA functionalization is specifically localised in the walls of the nanoporous {beta}-PVDF membrane by grafting. The PAA is a cation exchange polymer that adsorbs metal ions, such as Pb{sup 2+}, from aqueous solutions concentrating the ions into the membrane. After a time the FME is transferred to an electrochemical cell for analysis. A negative potential is applied to the Au film of the FME for a set time to reduce the adsorbed ions onto the Au film working electrode. The other metalized side of the FME functions as a counter electrode. Finally, square-wave anodic stripping voltammetry (SW-ASV) is performed on the FME to determine the metal ion concentrations in the original solution. The calibration curve of charge versus log concentration has a Temkin isotherm form. The FME membranes are 9 {mu}m thick and have 40 nm diameter pores with a density of 10{sup 10} pores/cm{sup 2}. This high pore density provides a large capacity for ion adsorption. Au ingress in the pores during sputtering forms a random array of nanoelectrodes. Like surface modified electrodes for adsorptive stripping voltammetry, the pre-concentration step for the FME is performed at open circuit. The zero current intercept of the calibration for Pb{sup 2+} is 0.13 ppb ({mu}g/L) and a detection limit of 0.050 ppb based on 3S/N from blank measurements. Voltammetry (CV) and chronoapmerometry (CA) were used to characterize the system. The apparent diffusion coefficient (D) for Pb{sup 2+} in the PAA functionalized pores was determined to be 2.44 x 10{sup -7} cm{sup 2}/s and the partition coefficient (p

Study of piezoelectric filler on the properties of PZT-PVDF composites

Science.gov (United States)

Matei, Alina; Å¢ucureanu, Vasilica; Vlǎzan, Paulina; Cernica, Ileana; Popescu, Marian; RomaniÅ£an, Cosmin

2017-12-01

The ability to obtain composites with desired functionalities is based on advanced knowledge of the processes synthesis and of the structure of piezoceramic materials, as well the incorporation of different fillers in selected polymer matrix. Polyvinylidene fluoride (PVDF) is a fluorinated polymer with excellent mechanical and electric properties, which it was chosen as matrix due to their applications in a wide range of industrial fields [1-4]. The present paper focuses on the development of composites based on PZT particles as filler obtained by conventional methods and PVDF as polymer matrix. The synthesis of PVDF-PZT composites was obtained by dispersing the ceramic powders in a solution of PVDF in N-methyl-pyrrolidone (NMP) under mechanical mixing and ultrasonication, until a homogenous mixture is obtained. The properties of the piezoceramic fillers before and after embedding into the polymeric matrix were investigated by Fourier transform infrared spectrometry, field emission scanning electron microscopy and X-ray diffraction. In the FTIR spectra, appear a large number of absorption bands which are exclusive of the phases from PVDF matrix confirming the total embedding of PZT filler into matrix. Also, the XRD pattern of the composites has confirmed the presence of crystalline phases of PVDF and the ceramic phase of PZT. The SEM results showed a good distribution of fillers in the matrix.

Self-Assembled Colloidal Particle Clusters from In Situ Pickering-Like Emulsion Polymerization via Single Electron Transfer Mechanism.

Science.gov (United States)

Yuan, Jinfeng; Zhao, Weiting; Pan, Mingwang; Zhu, Lei

2016-08-01

A simple route is reported to synthesize colloidal particle clusters (CPCs) from self-assembly of in situ poly(vinylidene fluoride)/poly(styrene-co-tert-butyl acrylate) [PVDF/P(St-co-tBA)] Janus particles through one-pot seeded emulsion single electron transfer radical polymerization. In the in situ Pickering-like emulsion polymerization, the tBA/St/PVDF feed ratio and polymerization temperature are important for the formation of well-defined CPCs. When the tBA/St/PVDF feed ratio is 0.75 g/2.5 g/0.5 g and the reaction temperature is 35 °C, relatively uniform raspberry-like CPCs are obtained. The hydrophobicity of the P(St-co-tBA) domains and the affinity of PVDF to the aqueous environment are considered to be the driving force for the self-assembly of the in situ formed PVDF/P(St-co-tBA) Janus particles. The resultant raspberry-like CPCs with PVDF particles protruding outward may be promising for superhydrophobic smart coatings. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Variation sweep rate cyclic voltammetry on the capacitance electrode activated carbon/PVDF with polymer electrolyte

Science.gov (United States)

Rohmawati, L.; Setyarsih, W.; Nurjannah, T.

2018-03-01

Sweep rate of the process voltammetry cyclic characterization is very influential towards the electrode capacitance value, especially on activated carbon electrodes/PVDF. A simple method of this research by use a mixing for electrode activated carbon/10 wt. % PVDF and the separator is made of a polymer electrolyte (PVA/H3PO4) by a sol gel method. The prototype supercapacitor is made in the form of a sandwich with a separator placed between two electrodes. Electrodes and separators are arranged in layers at a pressure of 1500 psi, then heated at 50°C for 10 minutes. Next done cyclic voltammetry in a potential range of -1 V to 1 V with a sweep rate of 5 mV/s, 10 mV/s, 20 mV/s, 25 mV/s and 50 mV/s. This results of curves voltammogram is reversible, the most wide curve on the sweep rate of 5 mV/s and most narrow curve on a sweep rate of 50 mV/s. Supercapacitor capacitance values obtained by 86 F/g, 43 F/g, 21 F/g, 16 F/g, and 8 F/g.

Figure of merit comparison of PP-based electret and PVDF-based piezoelectric polymer energy harvesters

Science.gov (United States)

Mrlík, M.; Leadenham, S.; AlMaadeed, M. A.; Erturk, A.

2016-04-01

The harvesting of mechanical strain and kinetic energy has received great attention over the past two decades in order to power wireless electronic components such as those used in passive and active monitoring applications. Piezoelectric ceramics, such as PZT (lead zirconate titanate), constitute the most commonly used electromechanical interface in vibration energy harvesters. However, there are applications in which piezoelectric ceramics cannot be used due to their low allowable curvature and brittle nature. Soft polymer PVDF (polyvinylidene fluoride) is arguably the most popular non-ceramic soft piezoelectric energy harvester material for such scenarios. Another type of polymer that has received less attention is PP (polypropylene) for electret-based energy harvesting using the thickness mode (33- mode). This work presents figure of merit comparison of PP versus PVDF for off-resonant energy harvesting in thickness mode operation, revealing substantial advantage of PP over PVDF. For thickness mode energy harvesting scenarios (e.g. dynamic compression) at reasonable ambient vibration frequencies, the figure of merit for the maximum power output is proportional to the square of the effective piezoelectric strain constant divided by the effective permittivity constant. Under optimal conditions and for the same volume, it is shown that PP can generate more than two orders of magnitude larger electrical power as compared to PVDF due to the larger effective piezoelectric strain constant and lower permittivity of the former.

Development of Polyvinylidene fluoride (PVDF)-ZIF-8 Membrane for Wastewater Treatment

Science.gov (United States)

Ibrahim, N. A.; Wirzal, M. D. H.; Nordin, N. A. H.; Halim, N. S. Abd

2018-04-01

Nowadays, the water shortage problem following the urbanization and increasing pollution of natural water source have increased the awareness to treat wastewater. Membrane filtration is often used in wastewater treatment plants to filter out more residual activated sludge from aeration process in the secondary stage. However, fouling is the main concern due to the fact it can happen to any membrane application. Antifouling properties in membrane can be improved by blending membranes with fillers or additives to make them more hydrophilic. This study aims to improve the antifouling properties in polyvinylidene fluoride (PVDF) membranes while optimizing the loading of Zeolitic imidazolate framework-8 (ZIF-8) fillers; at different loading (2.0 wt. %, 4.0 wt. %, 6.0 wt. %, 8.0 wt. % and 10.0 wt. %). Manual hand-casting of flat sheet membrane was done and the fabricated membranes were tested for their filterability against pure water and domestic wastewater. Both permeability tests showed that PVDF with 8% ZIF-8 membrane was the most permeable with a pure water and wastewater permeability of 150 L/m2.h.bar and 94 L/m2.h.bar, respectively. The pure water permeability of PVDF with 8% ZIF-8 membrane increases for about 130% compared to the pure PVDF membrane. The turbidity test of the initial feed and final permeate of wastewater, PVDF with 8% ZIF-8 membrane also gave out the highest reduction rate at 87%, which is 36% higher than that of pure PVDF membrane. It can be deduced that 8% of ZIF-8 is the ideal loading to PVDF in improving its antifouling properties to be used in domestic wastewater treatment.

Growth of BaTiO3-PVDF composite thick films by using aerosol deposition

Science.gov (United States)

Cho, Sung Hwan; Yoon, Young Joon

2016-01-01

Barium titanate (BaTiO3)-polyvinylidene fluoride (PVDF) composite thick films were grown by using aerosol deposition at room temperature with BaTiO3 and PVDF powders. To produce a uniform composition in ceramic and polymer composite films, which show a substantial difference in specific gravity, we used PVDF-coated BaTiO3 powders as the starting materials. An examination of the microstructure confirmed that the BaTiO3 were well distributed in the PVDF matrix in the form of a 0 - 3 compound. The crystallite size in the BaTiO3-PVDF composite thick films was 5 ˜ 50 times higher than that in pure BaTiO3 thick films. PVDF plays a role in suppressing the fragmentation of BaTiO3 powder during the aerosol deposition process and in controlling the relative permittivity.

Enhanced Lithium- and Sodium-Ion Storage in an Interconnected Carbon Network Comprising Electronegative Fluorine.

Science.gov (United States)

Hong, Seok-Min; Etacheri, Vinodkumar; Hong, Chulgi Nathan; Choi, Seung Wan; Lee, Ki Bong; Pol, Vilas G

2017-06-07

Fluorocarbon (C x F y ) anode materials were developed for lithium- and sodium-ion batteries through a facile one-step carbonization of a single precursor, polyvinylidene fluoride (PVDF). Interconnected carbon network structures were produced with doped fluorine in high-temperature carbonization at 500-800 °C. The fluorocarbon anodes derived from the PVDF precursor showed higher reversible discharge capacities of 735 mAh g -1 and 269 mAh g -1 in lithium- and sodium-ion batteries, respectively, compared to the commercial graphitic carbon. After 100 charge/discharge cycles, the fluorocarbon showed retentions of 91.3% and 97.5% in lithium (at 1C) and sodium (at 200 mA g -1 ) intercalation systems, respectively. The effects of carbonization temperature on the electrochemical properties of alkali metal ion storage were thoroughly investigated and documented. The specific capacities in lithium- and sodium-ion batteries were dependent on the fluorine content, indicating that the highly electronegative fluorine facilitates the insertion/extraction of lithium and sodium ions in rechargeable batteries.

Using PVDF for wavenumber-frequency analysis and excitation of guided waves

Science.gov (United States)

Ren, Baiyang; Cho, Hwanjeong; Lissenden, Cliff J.

2018-04-01

The role of transducers in nondestructive evaluation using ultrasonic guided waves cannot be overstated. Energy conversion from electrical to mechanical for actuation and then back to electrical for signal processing broadly describes transduction, but there are many other aspects of transducers that determine their effectiveness. Recently we have reported on polyvinylidene difluoride (PVDF) array sensors that enable determination of the wavenumber spectrum, which enables modal content in the received signal to be characterized. Modal content is an important damage indicator because, for example, mode conversion is a frequent consequence of wave interaction with defects. Some of the positive attributes of PVDF sensors are: broad frequency bandwidth, compliance for use on curved surfaces, limited influence on the passing wave, minimal cross-talk between elements, low profile, low mass, and inexpensive. The anisotropy of PVDF films also enables them to receive either Lamb waves or shear horizontal waves by proper alignment of the material principal coordinate axes. Placing a patterned set of electrodes on the PVDF film provides data from an array of elements. A linear array of elements is used to enable a 2D fast Fourier transform to determine the wavenumber spectrum of both Lamb waves and shear horizontal waves in an aluminum plate. Moreover, since PVDF film can sustain high voltage excitation, high power pulsers can be used to improve the signal-to-noise ratio. The capability of PVDF as a transmitter has been demonstrated with high voltage excitation.

Comb-like temperature-responsive polyhydroxyalkanoate-graft-poly(2-dimethylamino-ethylmethacrylate) for controllable protein adsorption

DEFF Research Database (Denmark)

Yao, Hui; Wei, Daixu; Che, Xuemei

2016-01-01

%. Graft copolymer PHA-g-PDMAEMA showed enhanced thermal stability, biocompatibility and controllable hydrophilicity compared with non-grafted P(3HDD-co-3H9D). The grafted material presented an obvious tendency of increasing protein adsorptions over the lower critical solution temperature (LCST 47.5 °C...... controllable protein adsorption for biomedical usages....

Enhanced binding by dextran-grafting to Protein A affinity chromatographic media.

Science.gov (United States)

Zhao, Lan; Zhu, Kai; Huang, Yongdong; Li, Qiang; Li, Xiunan; Zhang, Rongyue; Su, Zhiguo; Wang, Qibao; Ma, Guanghui

2017-04-01

Dextran-grafted Protein A affinity chromatographic medium was prepared by grafting dextran to agarose-based matrix, followed by epoxy-activation and Protein A coupling site-directed to sulfhydryl groups of cysteine molecules. An enhancement of both the binding performance and the stability was achieved for this dextran-grafted Protein A chromatographic medium. Its dynamic binding capacity was 61 mg immunoglobulin G/mL suction-dried gel, increased by 24% compared with that of the non-grafted medium. The binding capacity of dextran-grafted medium decreased about 7% after 40 cleaning-in-place cycles, much lower than that of the non-grafted medium as decreased about 15%. Confocal laser scanning microscopy results showed that immunoglobulin G was bound to both the outside and the inside of dextran-grafted medium faster than that of non-grafted one. Atomic force microscopy showed that this dextran-grafted Protein A medium had much rougher surface with a vertical coordinate range of ±80 nm, while that of non-grafted one was ±10 nm. Grafted dextran provided a more stereo surface morphology and immunoglobulin G molecules were more easily to be bound. This high-performance dextran-grafted Protein A affinity chromatographic medium has promising applications in large-scale antibody purification. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Modification of macroporous membranes by graft co-polymerization induced by pre-irradiation with an electron accelerator

International Nuclear Information System (INIS)

Grasselli, M.; Yoshii, Fumio

1999-01-01

Glycidyl methacrylate (GMA) and N,N-dimethylacrylamide (DMAA) have been co-grafted on hollow fiber membranes of macroporous polyethylene. Grafted copolymers have been obtained with different ratios of the monomers (molar ratio between 0 and 2 DMAA/GMA). The properties of the modified membranes are studied

Prognostic information in administrative co-morbidity data following coronary artery bypass grafting

DEFF Research Database (Denmark)

Abildstrøm, Steen Zabell; Hvelplund, Anders; Rasmussen, Søren

2010-01-01

Objectives: The aim of this study was to evaluate the prognostic information obtainable from administrative data with respect to 30-day mortality following coronary artery bypass grafting (CABG) and to compare it with the European System for Cardiac Operative Risk Evaluation (EuroSCORE) recorded ...... was equal to that of the EuroSCORE (c-statistic 0.79). Conclusions: A standard co-morbidity index based on administrative data as well as on clinical data has proven equally useful for prediction of mortality amongst CABG patients.......Objectives: The aim of this study was to evaluate the prognostic information obtainable from administrative data with respect to 30-day mortality following coronary artery bypass grafting (CABG) and to compare it with the European System for Cardiac Operative Risk Evaluation (EuroSCORE) recorded...... in a clinical database. Methods: We used a co-morbidity index calculated from administrative data in the Danish National Patient Register by means of all admissions 1 year prior to CABG. In addition, each CABG was categorised as being isolated or not, and acute or not. The prognostic power of the co...

Flocculation and adsorption properties of biodegradable gum-ghatti-grafted poly(acrylamide-co-methacrylic acid) hydrogels

CSIR Research Space (South Africa)

Mittal, H

2015-01-01

Full Text Available This study reports the microwave-assisted synthesis of gum-ghatti (Gg)-grafted poly(acrylamide-co-methacrylic acid) (AAm-co-MAA) hydrogels for the development of biodegradable flocculants and adsorbents. The synthesized hydrogels were characterized...

Synthesis, Structural, Optical and Dielectric Properties of Nanostructured 0-3 PZT/PVDF Composite Films.

Science.gov (United States)

Revathi, S; Kennedy, L John; Basha, S K Khadheer; Padmanabhan, R

2018-07-01

Nanostructured PbZr0.52Ti0.48O3 (PZT) powder was synthesized at 500 °C-800 °C using sol-gel route. X-ray diffraction and Rietveld analysis confirmed the formation of perovskite structure. The sample heat treated at 800 °C alone showed the formation of morphotropic phase boundary with coexistence of tetragonal and rhombohedral phase. The PZT powder and PVDF were used in 0-3 connectivity to form the PZT/PVDF composite film using solvent casting method. The composite films containing 10%, 50%, 70% and 80% volume fraction of PZT in PVDF were fabricated. The XRD spectra validated that the PZT structure remains unaltered in the composites and was not affected by the presence of PVDF. The scanning electron microscopy images show good degree of dispersion of PZT in PVDF matrix and the formation of pores at higher PZT loading. The quantitative analysis of elements and their composition were confirmed from energy dispersive X-ray analysis. The optical band gap of the PVDF film is 3.3 eV and the band gap decreased with increase in volume fraction of PZT fillers. The FTIR spectra showed the bands corresponding to different phases of PVDF (α, β, γ) and perovskite phase of PZT. The thermogravimetric analysis showed that PZT/PVDF composite films showed better thermal stability than the pure PVDF film and hydrophobicity. The dielectric constant was measured at frequency ranging from 1 Hz to 6 MHz and for temperature ranging from room temperature to 150 °C. The composite with 50% PZT filler loading shows the maximum dielectric constant at the studied frequency and temperature range with flexibility.

Poling of PVDF matrix composites for integrated structural load sensing

Science.gov (United States)

Haghiashtiani, Ghazaleh; Greminger, Michael A.; Zhao, Ping

2014-03-01

The purpose of this study is to create and evaluate a smart composite structure that can be used for integrated load sensing and structural health monitoring. In this structure, PVDF films are used as the matrix material instead of epoxy resin or other thermoplastics. The reinforcements are two layers of carbon fiber with one layer of Kevlar separating them. Due to the electrical conductivity properties of carbon fiber and the dielectric effect of Kevlar, the structure acts as a capacitor. Furthermore, the piezoelectric properties of the PVDF matrix can be used to monitor the response of the structure under applied loads. In order to exploit the piezoelectric properties of PVDF, the PVDF material must be polarized to align the dipole moments of its crystalline structure. The optimal condition for poling the structure was found by performing a 23 factorial design of experiment (DoE). The factors that were studied in DoE were temperature, voltage, and duration of poling. Finally, the response of the poled structure was monitored by exposing the samples to an applied load.

Preparation of high water-swelling agricultural starch hydrogels by 60Co γ-radiation grafting

International Nuclear Information System (INIS)

Wang Qingjun; Quan Yiwu; Chen Qingmin

2003-01-01

The starch grafted acrylic acid was used to synthesize water-swelling hydrogels by 60 Co γ-radiation grafting technique. With radiation dose of about 7 kGy, the crosslinking reagent amount of 0.001%-0.1%, the pH value 5-8 and the starch amount of 10%-30%, we can produce 600 times water-swelling hydrogels which are of high performance, low cost and suitable for agriculture

The Modification of PVDF Membrane via Crosslinking with Chitosan and Glutaraldehyde as the Crosslinking Agent

OpenAIRE

Silitonga, Romaya Sitha; Widiastuti, Nurul; Jaafar, Juhana; Ismail, Ahmad Fauzi; Abidin, Muhammad Nidzhom Zainol; Azelee, Ihsan Wan; Naidu, Mahesan

2018-01-01

Poly(vinylidene fluoride) (PVDF) has outstanding properties such as high thermal stability, resistance to acid solvents and good mechanical strength. Due to its properties, PVDF is widely used as a membrane matrix. However, PVDF membrane is hydrophobic properties, so as for specific applications, the surface of membrane needs to be modified to become hydrophilic. This research aims to modify PVDF membrane surface with chitosan and glutaraldehyde as a crosslinker agent. The FTIR spectra showed...

Surface energy characteristics of zeolite embedded PVDF nanofiber films with electrospinning process

Science.gov (United States)

Kang, Dong Hee; Kang, Hyun Wook

2016-11-01

Electrospinning is a nano-scale fiber production method with various polymer materials. This technique allows simple fiber diameters control by changing the physical conditions such as applied voltage and polymer solution viscosity during the fabrication process. The electrospun polymer fibers form a thin porous film with high surface area to volume ratio. Due to these unique characteristics, it is widely used for many application fields such as photocatalyst, electric sensor, and antibacterial scaffold for tissue engineering. Filtration is one of the main applications of electrospun polymer fibers for specific application of filtering out dust particles and dehumidification. Most polymers which are commonly used in electrospinning are hard to perform the filtering and dehumidification simultaneously because of their low hygroscopic property. To overcome this obstacle, the desiccant polymers are developed such as polyacrylic acid and polysulfobetaine methacrylate. However, the desiccant polymers are generally expensive and need special solvent for electrospinning. An alternating way to solve these problems is mixing desiccant material like zeolite in polymer solution during an electrospinning process. In this study, the free surface energy characteristics of electrospun polyvinylidene fluoride (PVDF) film with various zeolite concentrations are investigated to control the hygroscopic property of general polymers. Fundamental physical property of wettability with PVDF shows hydrophobicity. The electrospun PVDF film with small weight ratio with higher than 0.1% of zeolite powder shows diminished contact angles that certifying the wettability of PVDF can be controlled using desiccant material in electrospinning process. To quantify the surface energy of electrospun PVDF films, sessile water droplets are introduced on the electrospun PVDF film surface and the contact angles are measured. The contact angles of PVDF film are 140° for without zeolite and 80° for with 5

Structural Changes of PVDF Membranes by Phase Separation Control

International Nuclear Information System (INIS)

Lee, Semin; Kim, Sung Soo

2016-01-01

Thermally induced phase separation (TIPS) and nonsolvent induced phase separation (NIPS) were simultaneously induced for the preparation of flat PVDF membranes. N-methyl-2-pyrrolidone (NMP) was used as a solvent and dibutyl-phthlate (DBP) was used as a diluent for PVDF. When PVDF was melt blended with NMP and DBP, crystallization temperature was lowered for TIPS and unstable region was expanded for NIPS. Ratio of solvent to diluent changed the phase separation mechanism to obtain the various membrane structures. Contact mode of dope solution with nonsolvent determined the dominant phase separation behavior. Since heat transfer rate was greater than mass transfer rate, surface structure was formed by NIPS and inner structure was by TIPS. Quenching temperature of dope solution also affected the phase separation mechanism and phase separation rate to result in the variation of structure

Graphene oxide reinforced poly (4-styrenesulfonic acid)/polyvinyl alcohol blend composites with enhanced dielectric properties for portable and flexible electronics

Energy Technology Data Exchange (ETDEWEB)

Deshmukh, Kalim, E-mail: deshmukh.kalim@gmail.com [Department of Physics, B.S. Abdur Rahman University, Chennai, 600048, TN (India); Ahamed, M. Basheer [Department of Physics, B.S. Abdur Rahman University, Chennai, 600048, TN (India); Sadasivuni, Kishor Kumar [Mechanical and Industrial Engineering Department, Qatar University, P.O. Box 2713, Doha (Qatar); Ponnamma, Deepalekshmi; AlMaadeed, Mariam Al-Ali [Center for Advanced Materials, Qatar University, P.O. Box 2713, Doha (Qatar); Khadheer Pasha, S.K. [Department of Physics, School of Advanced Sciences, VIT University, Vellore, 632014, TN (India); Deshmukh, Rajendra R. [Department of Physics, Institute of Chemical Technology, Matunga, Mumbai, 400019 (India); Chidambaram, K. [Department of Physics, School of Advanced Sciences, VIT University, Vellore, 632014, TN (India)

2017-01-15

In this work, Graphene Oxide (GO) reinforced novel polymer composites comprising of poly (4-styrenesulfonic acid) (PSSA) and polyvinyl alcohol (PVA) blend matrix have been developed using colloidal processing technique. The properties and the structure of prepared composites were investigated using Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction (XRD), UV–vis spectroscopy (UV), Thermogravimetric analysis (TGA), Polarized optical microscopy (POM), Scanning electron microscopy (SEM) and Atomic force microscopy (AFM). The FTIR and Raman spectroscopy analysis indicate the strong interfacial interaction between GO and PSSA/PVA blend matrix. The XRD and SEM analysis confirm that GO was fully exfoliated into individual graphene sheets and dispersed homogeneously within the polymer matrix. The effective reinforcement of GO into PSSA/PVA blend matrix has resulted in the enhancement of dielectric constant. The dielectric constant has increased from 82.67 (50 Hz, 150 °C) for PSSA/PVA (50/50) blend to 297.91 (50 Hz, 150 °C) for PSSA/PVA/GO composites with 3 wt % GO loading. The dielectric loss (tan δ) has increased from 1.56 (50 KHz, 140 °C) for PSSA/PVA (50/50) blend to 2.64 (50 KHz, 140 °C) for PSSA/PVA/GO composites with 3 wt % GO loading. These findings provide a new insight to fabricate flexible, high-k dielectric composite as a promising material for energy storage applications. - Highlights: • Graphene Oxide was prepared from natural graphite using modified Hummers method. • Novel PSSA/PVA/GO composites were prepared by reinforcing GO into PSSA/PVA blend matrix. • Molecular level dispersion of GO in PSSA/PVA blend matrix was successfully achieved. • Enhancement in the dielectric constant was observed due to effective reinforcement of GO in PSSA/PVA blend matrix. • PSSA/PVA/GO composites with high dielectric performances can be considered for energy storage applications.

The preparation of highly absorbing cellulosic copolymers -the cellulose acetate/propionate-g.co-acrylic acid system

International Nuclear Information System (INIS)

Bilgin, V.; Guthrie, J.T.

1990-01-01

A series of copolymers based on the cellulose acetate/propionate-g.co-acrylic acid system has been prepared under radiation-induced control. These copolymers have been assessed for their water-retention capacity both in an unmodified state and after ''decrystallization'' or ''neutralization'' treatments. The grafting of acrylic acid onto the cellulose acetate/propionate had little effect on the water retention power of the cellulose acetate/propionate. However, improvements to the water retentivity was obtained after ''decrystallization'' procedures had been carried out on the copolymers using selected alkali metal salts with methanol as the continuous medium. The water-retentivity of the copolymers increased with increase in the extent of grafting, though the effect is less pronounced at high graft levels. Neutralization of the functional groups of the grafted branches provided a route to obtaining a marked increase in the level of water retentivity. Excessive salt concentrations gave reduced levels of water retentivity. Cesium carbonate and sodium carbonate have been shown to be effective in providing marked improvements in the water-retaining capacity of the copolymers. Maxima in performance are shown with respect to the treatment conditions. (author)

PDMS/PVDF hybrid electrospun membrane with superhydrophobic property and drop impact dynamics for dyeing wastewater treatment using membrane distillation

KAUST Repository

An, Alicia Kyoungjin

2016-10-21

Fouling in membrane distillation (MD) results in an increase in operation costs and deterioration in a water quality. In this work, a poly(vinylidene fluoride-co-hexafluoropropene) (PVDF-HFP) electrospun (E-PH) membrane was fabricated by hybridizing polydimethylsiloxane (PDMS) polymeric microspheres with superhydrophobicity onto the E-PH membrane via electrospinning. The resulting hybrid PDMS with E-PH (E-PDMS) membrane showed a significant enhancement in surface hydrophobicity (contact angle, CA = 155.4°) and roughness (Ra = 1,285mm). The zeta potential of E-PDMS membrane surface showed a higher negative value than that of a commercial PVDF (C-PVDF) membrane. These properties of E-PDMS membrane provided an antifouling in treating of differently-charged dyes and generated a flake-like dye–dye (loosely bound foulant) structure on the membrane surface rather than in the membrane pores. This also led to a high productivity of E-PDMS membrane (34 Lm-2h-1, 50% higher than that of C-PVDF membrane) without fouling or wetting. In addition, complete color removal and pure water production were achieved during a long-term operation. An application of intermittent water flushing (WF) in direct contact MD (DCMD) operation led to a 99% CA recovery of E-PDMS membrane indicating its sustainability. Therefore, the E-PDMS membrane is a promising candidate for MD application in dyeing wastewater treatment.

New CO2 adsorbent containing aminated poly(glycidyl methacrylate) grafted onto irradiated PE-PP nonwoven sheet

Science.gov (United States)

Mahmoud Nasef, Mohamed; Abbasi, Ali; Ting, T. M.

2014-10-01

A new CO2 adsorbent containing triethylamine (TEA) was prepared by radiation induced grafting of glycidyl methacrylate (GMA) onto polyethylene coated polypropylene (PE-PP) non-woven sheet followed by amination reaction. The degree of grafting (DOG%) was controlled by variation of monomer concentration and absorbed dose. The incorporation of aminated poly(GMA) was investigated by Fourier transform infrared (FTIR) and scanning electron microscope (SEM). The adsorbent with DOG of 350% and amination yield of 60% exhibited CO2 adsorption capacity of 4.52 mol/kg at ambient temperature and pressure.

Flexible Pressure Sensor Based on PVDF Nanocomposites Containing Reduced Graphene Oxide-Titania Hybrid Nanolayers

Directory of Open Access Journals (Sweden)

Aisha Al-Saygh

2017-01-01

Full Text Available A novel flexible nanocomposite pressure sensor with a tensile strength of about 47 MPa is fabricated in this work. Nanolayers of titanium dioxide (titania nanolayers, TNL synthesized by hydrothermal method are used to reinforce the polyvinylidene fluoride (PVDF by simple solution mixing. A hybrid composite is prepared by incorporating the TNL (2.5 wt % with reduced graphene oxide (rGO (2.5 wt % synthesized by improved graphene oxide synthesis to form a PVDF/rGO-TNL composite. A comparison between PVDF, PVDF/rGO (5 wt %, PVDF/TNL (5 wt % and PVDF/rGO-TNL (total additives 5 wt % samples are analyzed for their sensing, thermal and dielectric characteristics. The new shape of additives (with sharp morphology, good interaction and well distributed hybrid additives in the matrix increased the sensitivity by 333.46% at 5 kPa, 200.7% at 10.7 kPa and 246.7% at 17.6 kPa compared to the individual PVDF composite of TNL, confirming its possible application in fabricating low cost and light weight pressure sensing devices and electronic devices with reduced quantity of metal oxides. Increase in the β crystallinity percentage and removal of α phase for PVDF was detected for the hybrid composite and linked to the improvement in the mechanical properties. Tensile strength for the hybrid composite (46.91 MPa was 115% higher than that of the neat polymer matrix. Improvement in the wettability and less roughness in the hybrid composites were observed, which can prevent fouling, a major disadvantage in many sensor applications.

PVDF nanofibers with silver nanoparticles and silver/titanium dioxide for antimicrobial applications;Eletrofiacao de nanofibras de PVDF com nanoparticulas de prata e de prata/dioxido de titanio para aplicacoes antimicrobiais

Energy Technology Data Exchange (ETDEWEB)

Costa, Ligia M.M.; Olyveira, Gabriel M. de, E-mail: gmolyveira@yahoo.com.b, E-mail: ligialmmc@hotmail.co [Universidade Federal de Sao Carlos (PPGCEM/UFScar), SP (Brazil). Programa de Pos Graduacao em Ciencia e Engenharia de Materiais; Gregorio Filho, Rinaldo; Pessan, Luiz A., E-mail: pessan@ufscar.b, E-mail: gregorio@ufscar.b [Universidade Federal de Sao Carlos (UFScar), SP (Brazil)

2009-07-01

PVDF nanofibers with and without nanoparticles were produced by the method of electro spinning using dimethylformamide (DMF). Silver nitrate nanoparticles (0,5 and 2 wt %) and silver/titanium dioxide nanoparticles obtained by the reduction method (2 wt %) were synthesized and added to the PVDF solution to prepared nanofibers. The processes of electrospinning and film preparation using PVDF with the nanoparticles were compared. Silver/titanium dioxide nanoparticles were characterized with X-ray diffraction (XRD), Scanning electron microscopy (SEM) with EDX and x-ray photoelectron spectroscopy (XPS) to show silver/titanium dioxide nanoparticles. Nanofibers mats were characterized with SEM to study the effects of the addition of the nanoparticles on the morphology behavior and spectroscopy by Fourier transform infrared (FTIR) to analyze the crystalline phase of PVDF films. (author)

Piezoelectric and optoelectronic properties of electrospinning hybrid PVDF and ZnO nanofibers

Science.gov (United States)

Ma, Jian; Zhang, Qian; Lin, Kabin; Zhou, Lei; Ni, Zhonghua

2018-03-01

Polyvinylidene fluoride (PVDF) is a unique ferroelectric polymer with significant promise for energy harvesting, data storage, and sensing applications. ZnO is a wide direct band gap semiconductor (3.37 eV), commonly used as ultraviolet photodetectors, nanoelectronics, photonicsand piezoelectric generators. In this study, we produced high output piezoelectric energy harvesting materials using hybrid PVDF/ZnO nanofibers deposited via electrospinning. The strong electric fields and stretching forces during the electrospinning process helps to align dipoles in the nanofiber crystal such that the nonpolar α-phase (random orientation of dipoles) is transformed into polar β-phase in produced nanofibers. The effect of the additional ZnO nanowires on the nanofiber β-phase composition and output voltage are investigated. The maximum output voltage generated by a single hybrid PVDF and ZnO nanofiber (33 wt% ZnO nanowires) is over 300% of the voltage produced by a single nanofiber made of pure PVDF. The ZnO NWs served not only as a piezoelectric material, but also as a semiconducting material. The electrical conductivity of the hybrid PVDF/ZnO nanofibers increased by more than a factor of 4 when exposed under ultraviolet (UV) light.

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

International Nuclear Information System (INIS)

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

2016-01-01

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 "1H nuclear magnetic resonance ("1H 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. - 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.

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.

Spectroscopic Investigation of the Canopy Configurations in Nanoparticle Organic Hybrid Materials of Various Grafting Densities during CO 2 Capture

KAUST Repository

Petit, Camille; Park, Youngjune; Lin, Kun-Yi Andrew; Park, Ah-Hyung Alissa

2012-01-01

Novel liquid-like nanoparticle organic hybrid materials (NOHMs) made of polyetheramine chains tethered onto functionalized silica nanoparticles were synthesized and characterized before and after exposure to CO 2 using NMR, Raman, and ATR FT-IR spectroscopies in order to investigate the effect of the grafting densities on the NOHM canopy structure. Considering the promising tunable properties for CO 2 capture of NOHMs, this study was conducted to provide important structural information to better design NOHMs for CO 2 capture. In order to minimize the CO 2 absorption via enthalpic effect and provide a more accurate assessment of the structural effects, the NOHMs were synthesized without task-specific groups. A greater chain ordering and decreased intermolecular interactions were observed in NOHMs compared to the unbound polymer. This was attributed to the specific structural arrangement of the frustrated canopy. The distinct configuration of grafted polymer chains caused different CO 2 packing and CO 2-induced swelling behaviors between the NOHMs and the unbound polymer. The grafting density influenced the ordering and coupling of the polymer chains and CO 2-induced swelling. Its effect on the CO 2 packing behavior was less pronounced. © 2011 American Chemical Society.

Spectroscopic Investigation of the Canopy Configurations in Nanoparticle Organic Hybrid Materials of Various Grafting Densities during CO 2 Capture

KAUST Repository

Petit, Camille

2012-01-12

Novel liquid-like nanoparticle organic hybrid materials (NOHMs) made of polyetheramine chains tethered onto functionalized silica nanoparticles were synthesized and characterized before and after exposure to CO 2 using NMR, Raman, and ATR FT-IR spectroscopies in order to investigate the effect of the grafting densities on the NOHM canopy structure. Considering the promising tunable properties for CO 2 capture of NOHMs, this study was conducted to provide important structural information to better design NOHMs for CO 2 capture. In order to minimize the CO 2 absorption via enthalpic effect and provide a more accurate assessment of the structural effects, the NOHMs were synthesized without task-specific groups. A greater chain ordering and decreased intermolecular interactions were observed in NOHMs compared to the unbound polymer. This was attributed to the specific structural arrangement of the frustrated canopy. The distinct configuration of grafted polymer chains caused different CO 2 packing and CO 2-induced swelling behaviors between the NOHMs and the unbound polymer. The grafting density influenced the ordering and coupling of the polymer chains and CO 2-induced swelling. Its effect on the CO 2 packing behavior was less pronounced. © 2011 American Chemical Society.

Structural, thermal and ion transport properties of radiation grafted lithium conductive polymer electrolytes

Energy Technology Data Exchange (ETDEWEB)

Nasef, Mohamed Mahmoud [Business and Advanced Technology Centre (BATC), Universiti Teknologi Malaysia, Jalan Semarak, 54100 Kuala Lumpur (Malaysia)]. E-mail: mahmoudeithar@mailcity.com; Saidi, Hamdani [Business and Advanced Technology Centre (BATC), Universiti Teknologi Malaysia, Jalan Semarak, 54100 Kuala Lumpur (Malaysia)

2006-10-10

Structural, thermal and ion transport properties of lithium conductive polymer electrolytes prepared by radiation-induced grafting of styrene onto poly(vinylidene fluoride) (PVDF) films and subsequent activation with LiPH{sub 6}/EC/DEC liquid electrolyte were investigated in correlation with the content of the grafted polystyrene (Y%). The changes in the structure were studied using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and differential scanning calorimetry (DSC). Thermal gravimetric analysis (TGA) was used to evaluate the thermal stability. The ionic conductivity was measured by means of ac impedance spectroscopy at various temperatures. The polymer electrolytes were found to undergo considerable structural and morphological changes that resulted in a noticeable increase in their ionic conductivity with the increase in Y% at various temperatures (25-65 deg. C). The ionic conductivity achieved a value of 1.61 x 10{sup -3} S cm{sup -1} when Y of the polymer electrolyte reached 50% and at 25 deg. C. The polymer electrolytes also showed a multi-step degradation behaviour and thermal stability up to 120 deg. C, which suits normal lithium battery operation temperature range. The overall results of this work suggest that the structural changes took place in PVDF matrix during the preparation of these polymer electrolytes have a strong impact on their various properties.

Fabrication of 6FDA-durene membrane incorporated with zeolite T and aminosilane grafted zeolite T for CO2/CH4 separation

Science.gov (United States)

Jusoh, Norwahyu; Fong Yeong, Yin; Keong Lau, Kok; Shariff, Azmi Mohd

2017-08-01

In the present work, zeolite T and aminosilane grafted zeolite T are embedded into 6FDA-durene polyimide phase for the fabrication of mixed matrix membranes (MMMs). FESEM images demonstrated that the improvement of interfacial adhesion between zeolite and polymer phases in MMM loaded with aminosilane grafted zeolite T was not significant as compared to zeolite T/6FDA-durene MMM. From the gas permeation test, CO2/CH4 selectivity up to 26.4 was achieved using MMM containing aminosilane grafted zeolite T, while MMM loaded with ungrafted zeolite T showed CO2/CH4 selectivity of 19.1. In addition, MMM incorporated with aminosilane grafted zeolite T particles successfully lies on Robeson upper bound 2008, which makes it an attractive candidate for CO2/CH4 separation.

Improvement of β-phase crystal formation in a BaTiO3-modified PVDF membrane

Science.gov (United States)

Lin, SHEN; Lei, GONG; Shuhua, CHEN; Shiping, ZHAN; Cheng, ZHANG; Tao, SHAO

2018-04-01

In this paper, low temperature plasma is used to modify the surface of barium titanate (BaTiO3) nanoparticles in order to enhance the interfacial compatibility between ferroelectric poly(vinylidene fluoride) (PVDF) and BaTiO3 nanoparticles. The results demonstrate that oxygenic groups are successfully attached to the BaTiO3 surface, and the quantity of the functional groups increases with the treatment voltage. Furthermore, the effect of modified BaTiO3 nanoparticles on the morphology and crystal structure of the PVDF/BaTiO3 membrane is investigated. The results reveal that the dispersion of BaTiO3 nanoparticles in the PVDF matrix was greatly improved due to the modification of the BaTiO3 nanoparticles by air plasma. It is worth noting that the formation of a β-phase in a PVDF/modified BaTiO3 membrane is observably promoted, which results from the strong interaction between PVDF chains and oxygenic groups fixed on the BaTiO3 surface and the better dispersion of BaTiO3 nanoparticles in the PVDF matrix. Besides, the PVDF/modified BaTiO3 membrane at the treatment voltage of 24 kV exhibits a lower water contact angle (≈68.4°) compared with the unmodified one (≈86.7°). Meanwhile, the dielectric constant of PVDF/BaTiO3 nanocomposites increases with the increase of working voltage.

Preparation and characterization of the PVDF-based composite membrane for direct methanol fuel cells

OpenAIRE

Qian Liu, Laizhou Song, Zhihui Zhang, Xiaowei Liu

2010-01-01

The polyvinylidene fluoride-sulfonated polystyrene composite membrane with proton exchange performance, denoted as PVDF-SPS, was prepared using a thermally induced polymerization technique. The thermal stability of the PVDF-SPS composite membrane was investigated using thermogravimetric (TG) analysis. The complex formation of the composite membrane was ascertained by Fourier transform infrared spectroscopy (FTIR). The surface compositions of the PVDF-SPS membrane were analyzed using X-ray pho...

Antimicrobial Activity of Two Garlic Species (Allium Sativum and A. Tuberosum) Against Staphylococci Infection. In Vivo Study in Rats.

Science.gov (United States)

Venâncio, Paulo César; Raimundo Figueroba, Sidney; Dias Nani, Bruno; Eduardo Nunes Ferreira, Luiz; Vilela Muniz, Bruno; de Sá Del Fiol, Fernando; Sartoratto, Adilson; Antonio Ribeiro Rosa, Edvaldo; Carlos Groppo, Francisco

2017-04-01

Purpose: This study observed the effect of garlic extracts and amoxicillin against an induced staphylococcal infection model. MIC and MBC were also obtained for aqueous extracts of Allium sativum (Asa) and Allium tuberosum (Atu) against Staphylococcus aureus penicillin-sensitive (PSSA - ATCC 25923) and MRSA (ATCC 33592). Methods: Granulation tissues were induced in the back of 205 rats. After 14 days, 0.5 mL of 10 8 CFU/mL of PSSA or MRSA were injected inside tissues. After 24h, animals were divided: G1 (Control) - 0.5 mL of NaCl 0.9%; G2 - Asa 100 mg/kg or 400mg/kg; G3 - Atu 100 mg/kg or 400 mg/kg; G4 - amoxicillin suspension 50 mg/kg, considering PSSA infection; and G5 (Control) - 0.5 mL of NaCl 0.9%; G6 - Asa 400mg/kg; G7 - amoxicillin 50 mg/kg; and G8 - Asa 400 mg/kg + amoxicillin 50 mg/kg for MRSA. All treatments were administered P.O. every 6h. Animals were killed at 0, 6, 12 and 24h. Samples were spread on salt-mannitol agar. Colonies were counted after 18 h at 37 °C. Atu was not able to inhibit or kill PSSA and MRSA. Considering Asa, MIC and MBC against PSSA were 2 mg/mL and 4 mg/mL, respectively; and 16 mg/mL and 64 mg/mL against MRSA. Results: No effect was observed in vivo for control, Asa 100 mg/kg and Atu 100 mg/kg, while amoxicillin, Atu 400 mg/kg and Asa 400 mg/kg decreased PSSA counts in all-time points. No effect of any group against MRSA was observed at any time. Conclusion: Thus, A. sativum and A. tuberosum were able to reduce PSSA infection, but not MRSA infection.

Flexible nano-GFO/PVDF piezoelectric-polymer nano-composite films for mechanical energy harvesting

Science.gov (United States)

Mishra, Monali; Roy, Amritendu; Dash, Sukalyan; Mukherjee, Somdutta

2018-03-01

Owing to the persistent quest of renewable energy technology, piezoelectric energy harvesters are gathering considerable research interest due to their potential in driving microelectronic devices with small power requirement. Electrical energy (milli to microwatt range) is generated from mechanical counterparts such as vibrations of machines, human motion, flowing water etc. based on the principles of piezoelectricity. Flexible high piezoelectric constant (d33) ceramic/polymer composites are crucial components for fabricating these energy harvesters. The polymer composites composed of gallium ferrite nanoparticles and polyvinylidene fluoride (PVDF) as the matrix have been synthesized by solvent casting method. First, 8 wt. % PVDF was dissolved in DMF and then different compositions of GaFeO3 or GFO (10, 20, 30 wt. %) (with respect to PVDF only) nanocomposites were synthesized. The phase of the synthesized nanocomposites were studied by X- Ray diffraction which shows that with the increase in the GFO concentration, the intensity of diffraction peaks of PVDF steadily decreased and GFO peaks became increasingly sharp. As the concentration of GFO increases in the PVDF polymer matrix, band gap is also increased albeit to a small extent. The maximum measured output voltage and current during mechanical pressing and releasing conditions were found to be ~ 3.5 volt and 4 nA, respectively in 30 wt % GFO-PVDF composite, comparable to the available literature.

Grafting of glycidyl methacrylate/styrene onto polyvinyldine fluoride membranes for proton exchange fuel cell

International Nuclear Information System (INIS)

Abdel-Hady, E.E.; El-Toony, M.M.; Abdel-Hamed, M.O.

2013-01-01

Simultaneous gamma irradiation was used effectively for grafting facilitation of glycidyl methacrylate (GMA) and styrene (Sty) onto polyvinylidine fluoride (PVDF). Grafting percent was 122 when monomers ratio are 30% Sty and 70% GMA at 20 KGy gamma irradiation dose. Characterization of the membrane was performed using FT-IR, ion exchange capacity (IEC), water uptake. Mechanical behavior such as tensile strength was studied while morphological structure of the membrane was carried out by scan electron microscope (SEM). The membrane with degree of grafting 122% showed higher IEC (1.2 m mol/cm) than those of Nafion membrane with corresponding proton conductivity of 5.7 × 10 −2 S/cm similar to it. Operating the fuel cell unit showed higher voltage of the prepared membranes than that of Nafion 211. The prepared membranes stability for 300 h work approved their applicability from the cost benefit point of view

Electric poling-assisted additive manufacturing process for PVDF polymer-based piezoelectric device applications

International Nuclear Information System (INIS)

Lee, ChaBum; Tarbutton, Joshua A

2014-01-01

This paper presents a new additive manufacturing (AM) process to directly and continuously print piezoelectric devices from polyvinylidene fluoride (PVDF) polymeric filament rods under a strong electric field. This process, called ‘electric poling-assisted additive manufacturing or EPAM, combines AM and electric poling processes and is able to fabricate free-form shape piezoelectric devices continuously. In this process, the PVDF polymer dipoles remain well-aligned and uniform over a large area in a single design, production and fabrication step. During EPAM process, molten PVDF polymer is simultaneously mechanically stresses in-situ by the leading nozzle and electrically poled by applying high electric field under high temperature. The EPAM system was constructed to directly print piezoelectric structures from PVDF polymeric filament while applying high electric field between nozzle tip and printing bed in AM machine. Piezoelectric devices were successfully fabricated using the EPAM process. The crystalline phase transitions that occurred from the process were identified by using the Fourier transform infrared spectroscope. The results indicate that devices printed under a strong electric field become piezoelectric during the EPAM process and that stronger electric fields result in greater piezoelectricity as marked by the electrical response and the formation of sharper peaks at the polar β crystalline wavenumber of the PVDF polymer. Performing this process in the absence of an electric field does not result in dipole alignment of PVDF polymer. The EPAM process is expected to lead to the widespread use of AM to fabricate a variety of piezoelectric PVDF polymer-based devices for sensing, actuation and energy harvesting applications with simple, low cost, single processing and fabrication step. (paper)

Triple-Layer Vascular Grafts Fabricated by Combined E-Jet 3D Printing and Electrospinning.

Science.gov (United States)

Huang, Ruiying; Gao, Xiangkai; Wang, Jian; Chen, Haoxiang; Tong, Chunyi; Tan, Yongjun; Tan, Zhikai

2018-05-29

Small-diameter tissue-engineered vascular grafts are urgently needed for clinic arterial substitute. To simulate the structures and functions of natural blood vessels, we designed a novel triple-layer poly(ε-caprolactone) (PCL) fibrous vascular graft by combining E-jet 3D printing and electrospinning techniques. The resultant vascular graft consisted of an interior layer comprising 3D-printed highly aligned strong fibers, a middle layer made by electrospun densely fibers, and an exterior structure composed of mixed fibers fabricated by co-electrospraying. The biocompatible triple-layer graft was used for in vivo implantation, and results demonstrated that the longitudinally-aligned fibers within the lumen of the graft could enhance the proliferation and migration of endothelial cells, while maintained good mechanical properties. The exterior layer provided a pathway that encouraged cells to migrate into the scaffold after implantation. This experimental graft overcame the limitations of conventionally electrospun vascular grafts of inadequate porosity and lowly cell penetration. The unique structure of the triple-layer vascular graft promoted cell growth and infiltration in vivo, thus provided an encouraging substitute for in situ tissue engineering.

Unique synergism in flame retardancy in ABS based composites through blending PVDF and halloysite nanotubes

Science.gov (United States)

Remanan, Sanjay; Sharma, Maya; Jayashree, Priyadarshini; Parameswaranpillai, Jyotishkumar; Fabian, Thomas; Shih, Julie; Shankarappa, Prasad; Nuggehalli, Bharath; Bose, Suryasarathi

2017-06-01

This study demonstrates flame retardant materials designed using bi-phasic polymer blends of acrylonitrile butadiene styrene (ABS) and polyvinylidene fluoride (PVDF) containing halloysite nanotubes (HNTs) and Cloisite 30B nanoclay. The prepared blends with and without nanoparticles were extensively characterized. The nanoparticles were added in different weight concentrations to improve the flame retardancy. It was observed that prepared ABS/PVDF blends showed better flame retardancy than ABS based composites. The flame resistance was further improved by the addition of nanoparticles in the blends. The microscale combustion calorimetry (MCC) test showed better flame resistance in ABS/PVDF blends filled with 5 wt% HNTs than other composites. The total heat release of ABS/PVDF blend filled with 5 wt% HNTs decreased by 31% and also the heat of combustion decreased by 26% as compared to neat ABS. When compared with nanoparticles, the addition of PVDF reduced the peak heat release rate (PHRR) and increased the char residue more effectively. A synergistic improvement was observed from both PVDF and HNTs on the flame resistance properties.

Investigation of ionic conduction in PEO-PVDF based blend polymer electrolytes

Science.gov (United States)

Patla, Subir Kumar; Ray, Ruma; Asokan, K.; Karmakar, Sanat

2018-03-01

We investigate the effect of blend host polymer on solid polymer electrolyte (SPE) films doped with ammonium iodide (NH4I) salt using a variety of experimental techniques. Structural studies on the composite SPEs show that the blending of Poly(ethylene oxide) (PEO)-Poly(vinylidene fluoride) (PVDF) polymers in a suitable ratio enhances the amorphous fraction of the polymer matrix and facilitates fast ion conduction through it. We observe that the addition of a small amount of PVDF in the PEO host polymer enhances the ion - polymer interaction leading to more ion dissociation. As a result, the effective number of mobile charge carriers within the polymer matrix increases. Systematic investigation in these blend SPEs shows that the maximum conductivity (1.01 × 10-3 S/cm) is obtained for PEO - rich (80 wt. % PEO, 20 wt. % PVDF) composites at 35 wt. % NH4I concentration at room temperature. Interestingly, at higher salt concentrations (above 35 wt. %), the conductivity is found to decrease in this system. The reduction of conductivity at higher salt concentrations is the consequence of decrease in the carrier concentration due to the formation of an ion pair and ion aggregates. PVDF-rich compositions (20 wt. % PEO and 80 wt. % PVDF), on the other hand, show a very complex porous microstructure. We also observe a much lower ionic conductivity (maximum ˜ 10-6 S/cm at 15 wt. % salt) in these composite systems relative to PEO-rich composites.

Obtention of graft copolymers by ionizing radiation, characterization and study of hemo-compatible properties

International Nuclear Information System (INIS)

Queiroz, A.A.A. de.

1993-01-01

The present work had as objectives the obtention and characterization of grafting copolymers by radiation induced polymerization and the study of its hemo compatible properties. The relationship between grafting conditions and anti-trombogenicity was examined for the purpose of clearing the necessity of controlling grafting conditions to enhance the copolymers blood compatibility. Two methods were chosen to accomplish the irradiation: mutual and pre-irradiation (peroxidation) of the films in 6O Co source and electron beam accelerator. Primarily grafting parameters were studied in the systems of the monomers N, N-dimethyl acrylamide (DMAA) and acrylic acid (AA) with the polymeric films: poly (tetrafluoroethylene) (PTFE), poly (ethylene-co-tetrafluoroethylene) (PETFE), low density polyethylene (LDPE) and poly (vinyl chloride) (PVC). The simultaneous irradiation was effective in the polymerization of all the substrates above mentioned, although the peroxidation method has given better results for PETFE-DMAA, LDPE-g-DMAA, LDPE-g-AA and PVC-g-AA. In the system AA/LDPE and AA/PVC the homo polymerization was controlled by the addition of the comonomer N, N-dimethyl acrylic acid (DMA). As for the grafting parameters, low dose rate and low irradiation dose, showed to be very effective for the graftability of DMAA and AA on the substrates. (author). 129 refs, 51 figs, 7 tabs

Impressive nonlinear optical response exhibited by Poly(vinylidene fluoride) (PVDF)/reduced graphene oxide (RGO) nanocomposite films

Science.gov (United States)

Sabira, K.; Saheeda, P.; Divyasree, M. C.; Jayalekshmi, S.

2017-12-01

In the present work, the nonlinear optical properties of free-standing films of Poly(vinylidene fluoride) (PVDF)/reduced graphene oxide (RGO) nanocomposite are investigated to assess their suitability as efficient optical limiters. The PVDF/RGO nanocomposite films are generated by mixing different concentrations of RGO as the filler, with PVDF, using solution casting method. The XRD and FTIR data of these nanocomposite films confirm the enhancement in the β phase of PVDF when RGO is added to PVDF, which is one of the prime factors, enhancing the nonlinear response of the nanocomposite. The open aperture and closed aperture Z-scan technique under nanosecond excitation (532 nm, 7 ns) is used to investigate the nonlinear optical characteristics of the PVDF/RGO nanocomposite films. These films are found to exhibit two photon absorption assisted optical non linearity in the nanosecond regime. The highlight of the present work is the observation of quite low values of the normalized transmittance and low optical limiting threshold power in free standing films of PVDF/RGO nanocomposite. These flexible, free-standing and stable nanocomposite films offer high application prospects in the design of efficient optical limiting devices of any desired size or shape.

3-D loaded scaffolds obtained by supercritical CO2 assisted process

Science.gov (United States)

Cardea, S.; Reverchon, E.

2014-08-01

In this work, a supercritical CO2 (SC-CO2) drying process for the formation of 3-D PVDF-HFP loaded scaffolds was tested. Experiments at pressures ranging between 150 and 250 bar and at temperatures ranging between 35 and 55°C were performed. The PVDF-HFP- acetone-ethanol solution at 15% w/w polymer was selected as the base case. The drug (amoxicillin) concentration was varied from 20 to 30% w/w with respect to PVDF-HFP. SC- CO2 drying process was confirmed to be a valid alternative to generate loaded structures; indeed, scaffolds characterized by nanometric networks (with mean pore diameter of about 300 nm) with a homogeneous drug distribution were obtained. Drug controlled release experiments were also performed and a quasi-zero order release kinetic was observed.

Kirigami-based PVDF thin-film as stretchable strain sensor

Science.gov (United States)

Hu, Nan; Chen, Dajing; Hao, Nanjing; Huang, Shicheng; Yu, Xiaojiao; Zhang, John X. J.; Chen, Zi

Kirigami, as the sister of the origami, involves cutting of 2D sheets to form complex 3D geometries with out-of-plane patterns. Motivated by the development of the high-stretchable biomedical devices, we explore the stretchability of the kirigami-based PVDF thin film under tension. Our structural prototypes include a set of 2D geometry with kirigami-based pattern cutting on PVDF thin films. We first used paper models to generate a wide range of cutting patterns to study the deformation under compression tests, the results of which are compared with finite element simulations. We then proceeded to test different kirigami-based designs to identify geometric parameters that can tune the post-buckling response and strain distribution. Next, we fabricated and tested the PVDF thin film with kirigami pattern. Experiments showed that the PVDF film in the absence of cutting can be stretched to a limited extent and will break upon further stretching. In contrast, the kirigami-based films can be stretched up to 100% without failure. Our designs demonstrate the ability to significantly improve the strain range of the structure and sensing ability of a sensor. We envision a promising future to use this class of structural elements to develop highly stretchable materials, structures, and devices. Z.C. acknowledges the Society in Science-Branco Weiss fellowship, administered by ETH Zürich. J.X.J.Z. acknowledges the NIH Director's Transformative Research Award (1R01 OD022910-01).

Nanoconfinement: an effective way to enhance PVDF piezoelectric properties.

Science.gov (United States)

Cauda, Valentina; Stassi, Stefano; Bejtka, Katarzyna; Canavese, Giancarlo

2013-07-10

The dimensional confinement and oriented crystallization are both key factors in determining the piezoelectric properties of a polymeric nanostructured material. Here we prepare arrays of one-dimensional polymeric nanowires showing piezoelectric features by template-wetting two distinct polymers into anodic porous alumina (APA) membranes. In particular, poly(vinylidene fluoride), PVDF, and its copolymer poly(vinylidene fluoride-trifluoroethylene), PVTF, are obtained in commercially available APA, showing a final diameter of about 200 nm and several micrometers in length, reflecting the templating matrix features. We show that the crystallization of both polymers into a ferroelectric phase is directed by the nanotemplate confinement. Interestingly, the PVDF nanowires mainly crystallize into the β-phase in the nanoporous matrix, whereas the reference thin film of PVDF crystallizes in the α nonpolar phase. In the case of the PVTF nanowires, needle-like crystals oriented perpendicularly to the APA channel walls are observed, giving insight on the molecular orientation of the polymer within the nanowire structure. A remarkable piezoelectric behavior of both 1-D polymeric nanowires is observed, upon recording ferroelectric polarization, hysteresis, and displacement loops. In particular, an outstanding piezoelectric effect is observed for the PVDF nanowires with respect to the polymeric thin film, considering that no poling was carried out. Current versus voltage (I-V) characteristics showed a consistent switching behavior of the ferroelectric polar domains, thus revealing the importance of the confined and oriented crystallization of the polymer in monodimensional nanoarchitectures.

Construction of a Fish-like Robot Based on High Performance Graphene/PVDF Bimorph Actuation Materials.

Science.gov (United States)

Xiao, Peishuang; Yi, Ningbo; Zhang, Tengfei; Huang, Yi; Chang, Huicong; Yang, Yang; Zhou, Ying; Chen, Yongsheng

2016-06-01

Smart actuators have many potential applications in various areas, so the development of novel actuation materials, with facile fabricating methods and excellent performances, are still urgent needs. In this work, a novel electromechanical bimorph actuator constituted by a graphene layer and a PVDF layer, is fabricated through a simple yet versatile solution approach. The bimorph actuator can deflect toward the graphene side under electrical stimulus, due to the differences in coefficient of thermal expansion between the two layers and the converse piezoelectric effect and electrostrictive property of the PVDF layer. Under low voltage stimulus, the actuator (length: 20 mm, width: 3 mm) can generate large actuation motion with a maximum deflection of about 14.0 mm within 0.262 s and produce high actuation stress (more than 312.7 MPa/g). The bimorph actuator also can display reversible swing behavior with long cycle life under high frequencies. on this basis, a fish-like robot that can swim at the speed of 5.02 mm/s is designed and demonstrated. The designed graphene-PVDF bimorph actuator exhibits the overall novel performance compared with many other electromechanical avtuators, and may contribute to the practical actuation applications of graphene-based materials at a macro scale.

Construction of a Fish‐like Robot Based on High Performance Graphene/PVDF Bimorph Actuation Materials

Science.gov (United States)

Xiao, Peishuang; Yi, Ningbo; Zhang, Tengfei; Chang, Huicong; Yang, Yang; Zhou, Ying

2016-01-01

Smart actuators have many potential applications in various areas, so the development of novel actuation materials, with facile fabricating methods and excellent performances, are still urgent needs. In this work, a novel electromechanical bimorph actuator constituted by a graphene layer and a PVDF layer, is fabricated through a simple yet versatile solution approach. The bimorph actuator can deflect toward the graphene side under electrical stimulus, due to the differences in coefficient of thermal expansion between the two layers and the converse piezoelectric effect and electrostrictive property of the PVDF layer. Under low voltage stimulus, the actuator (length: 20 mm, width: 3 mm) can generate large actuation motion with a maximum deflection of about 14.0 mm within 0.262 s and produce high actuation stress (more than 312.7 MPa/g). The bimorph actuator also can display reversible swing behavior with long cycle life under high frequencies. on this basis, a fish‐like robot that can swim at the speed of 5.02 mm/s is designed and demonstrated. The designed graphene‐PVDF bimorph actuator exhibits the overall novel performance compared with many other electromechanical avtuators, and may contribute to the practical actuation applications of graphene‐based materials at a macro scale. PMID:27818900

Prevention of graft-versus-host-disease with preserved graft-versus-leukemia-effect by ex vivo and in vivo modulation of CD4(+) T-cells.

Science.gov (United States)

Fricke, Stephan; Hilger, Nadja; Fricke, Christian; Schönfelder, Uta; Behre, Gerhard; Ruschpler, Peter; Boldt, Andreas; Oelkrug, Christopher; Sack, Ulrich; Emmrich, Frank

2014-06-01

This is the first report showing that an epitope-specific ex vivo modulation of an allogeneic hematopoietic stem cell graft by the anti-human CD4 antibody MAX.16H5 IgG1 simultaneously facilitates the anti-tumor capacity of the graft (Graft-versus-leukemia effect, GvL) and the long-term suppression of the deleterious side effect Graft-versus-host-disease (GvHD). To distinguish and consolidate GvL from GvHD, the anti-human CD4 antibody MAX16.H5 IgG1 was tested in murine GvHD and tumor models. The survival rate was significantly increased in recipients receiving a MAX.16H5 IgG1 short-term (2 h) pre-incubated graft even when tumor cells were co-transplanted or when recipient mice were treated by MAX.16H5 IgG1 before transplantation. After engraftment, regulatory T-cells are generated only supporting the GvL effect. It was also possible to transfer the immune tolerance from GvHD-free recipient chimeras into third party recipient mice without the need of reapplication of MAX.16H5 IgG1 anti-human CD4 antibodies. These findings are also benefical for patients with leukemia when no matched related or unrelated donor is available and provides a safer allogeneic HSCT, which is more effective against leukemia. It also facilitates allogeneic (stem) cell transplantations for other indications (e.g., autoimmune-disorders).

Effect of electron beam irradiation on structural and thermal properties of gamma poly (vinylidene fluoride) (γ-PVDF) films

Science.gov (United States)

Tan, Zhongyang; Wang, Xuemei; Fu, Chao; Chen, Chunhai; Ran, Xianghai

2018-03-01

In this study, we successfully prepared the pure PVDF film containing almost exclusive γ-phase (γ-PVDF) using 15 wt% solution in N, N-dimethylformamide. These γ-PVDF films were irradiated by 3.0 MeV electron beam in vacuum at room temperature up to 358 kGy. The effect of the irradiation on the chemical structural and thermal properties of pristine and irradiated γ-PVDF films were detailedly investigated by FTIR, XRD and DSC, respectively. DSC results show that two single and different melting endotherms from the successive heating curves correspond to γ-phase and α-phase, respectively. FTIR results show that the characteristic absorption peaks corresponding to γ-phase do not shift, and the C˭C bond formation is not significantly observed in the irradiated γ-PVDF films until above 30 kGy. XRD results show that the crystal form of γ-PVDF is not influenced significantly by irradiation. All PVDF films exhibit a single melting endotherm, irrespective of the irradiation dose. Two superpositioned crystallization peaks were observed for PVDF films only irradiated at high dose of 232 and 358 kGy, which can be related to the fractionated crystallization of irradiated PVDF. The dependences of thermal characteristics on the irradiation dose were detailedly investigated by DSC in this study.

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

International Nuclear Information System (INIS)

Kiatkamjornwong, Suda; Mongkolsawat, Kanlaya; Sonsuk, Manit

2004-01-01

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

Modification of phase transitions in swift heavy ion irradiated and MMA-grafted ferroelectric fluoro-polymers

International Nuclear Information System (INIS)

Petersohn, E.; Betz, N.; Le Moel, A.

1994-01-01

Ferroelectric polyvinylidene fluoride (β) and copolymers of vinylidene fluoride trifluoroethylene (P(VDF/TrFE)) films were irradiated with swift heavy ions and post irradiation grafted with methyl methacrylate (MMA). We have studied the influence of irradiation parameters such as the ion fluence, the type of ion and the electronic stopping power, on the melting and crystallization temperatures and the ferroelectric-paraelectric phase transitions, by differential scanning calorimetry (DSC) and dielectric measurements. The relation between the shift in the transition temperatures and the ion fluence is described by a single term equation. Ion track grafting with MMA affects the ferroelectric-paraelectric phase transitions in P(VDF/TrFE) and leads to a strong amorphization of the polymer films. The grafting in β PVDF occurs mainly on the surface of the samples and no change in the transition temperatures is observed. (authors). 12 refs., 6 figs., 2 tabs

Organic fouling behavior of superhydrophilic polyvinylidene fluoride (PVDF) ultrafiltration membranes functionalized with surface-tailored nanoparticles: Implications for organic fouling in membrane bioreactors

KAUST Repository

Liang, Shuai

2014-08-01

This study systematically investigates the organic fouling behavior of a superhydrophilic polyvinylidene fluoride (PVDF) ultrafiltration membrane functionalized via post-fabrication tethering of surface-tailored silica nanoparticles to poly(methacrylic acid)-grafted PVDF membrane surface. Sodium alginate (SA), Suwannee River natural organic matter (SRNOM), and bovine serum albumin (BSA) were used as model organic foulants to investigate the antifouling behavior of the superhydrophilic membrane with combined-fouling (mixture of foulants) and individual-fouling (single foulant) tests. A membrane bioreactor (MBR) plant supernatant was also used to verify the organic antifouling property of the superhydrophilic membrane under realistic conditions. Foulant size distributions and foulant-membrane interfacial forces were measured to interpret the observed membrane fouling behavior. Molecular weight cutoff measurements confirmed that membrane functionalization did not adversely affect the intrinsic membrane selectivity. Both filtration tests with the synthetic foulant-mixture solution (containing SA, SRNOM, and BSA) and MBR plant supernatant demonstrated the reliability and durability of the antifouling property of the superhydrophilic membrane. The conspicuous reduction in foulant-membrane interfacial forces for the functionalized membrane further verified the antifouling properties of the superhydrophilic membrane, suggesting great potential for applications in wastewater treatment. © 2014 Elsevier B.V.

Fabrication and characterization of a novel hydrophobic CaCO{sub 3} grafted by hydroxylated poly(vinyl chloride) chains

Energy Technology Data Exchange (ETDEWEB)

Bao, Lixia [State Key Laboratory of Polymer Materials Engineering, Sichuan University (China); School of Chemical Science and Technology, Yunnan University (China); Yang, Simei; Luo, Xin [School of Chemical Science and Technology, Yunnan University (China); Lei, Jingxin [State Key Laboratory of Polymer Materials Engineering, Sichuan University (China); Cao, Qiue [School of Chemical Science and Technology, Yunnan University (China); Wang, Jiliang, E-mail: jlwang@ynu.edu.cn [School of Chemical Science and Technology, Yunnan University (China)

2015-12-01

Highlights: • Hydroxylated poly(vinyl chloride) (PVC-OH) with different molecular weight and hydroxyl value was successfully prepared by the suspension copolymerization. • PVC-OH was grafted onto the surface of CaCO{sub 3} particles by the urethane formation reaction. • The modified CaCO{sub 3} particles show excellent hydrophobicity. - Abstract: The hydroxylated PVC (PVC-OH) was successfully synthesized by a suspension polymerization of vinyl chloride (VC), butyl acrylate (BA) and hydroxyethyl acrylate (HEA). Novel hydrophobic CaCO{sub 3} was then prepared by a urethane formation reaction between methylene diphenyl diisocyanate (MDI) and the −OH groups both in the PVC-OH chains and on the surface of pristine CaCO{sub 3} particles. The effect of the PVC-OH content on the grafting ratio of treated CaCO{sub 3} particles was extensively investigated. Combining the result of Fourier transform infrared (FTIR) with that of water contact angle, it can be concluded that the hydrophobicity of CaCO{sub 3} had been efficiently improved by the PVC-OH segments grafted on the surface of CaCO{sub 3} particles. X-ray diffraction (XRD), thermal gravity analysis (TGA), scanning electron microscope (SEM) and transmission electron microscope (TEM) were also used to study crystalline behaviors, thermal stability and surface morphology of the modified CaCO{sub 3} particles, respectively. The change of specific surface area implying surface modification was investigated as well.

Preliminary Study on the Removal of Steroidal Estrogens Using TiO2-Doped PVDF Ultrafiltration Membranes

Directory of Open Access Journals (Sweden)

Mingquan Wang

2016-04-01

Full Text Available Steroidal estrogens are a representative type of endocrine-disrupting chemical contaminant that has been detected in surface water. In this paper, modified polyvinylidene fluoride (PVDF membranes were prepared by adding different amounts of polyvinyl pyrrolidone (PVP and nano-TiO2 particles. PVDF-PVP membrane adsorption, UV photolysis and PVDF-PVP-TiO2 membrane photocatalysis performance were investigated by considering the rejection of estrone (E1 and 17β-estradiol (E2 in the cross-flow filtration experiments. The mechanism of photocatalytic degradation on TiO2-doped PVDF membranes was also evaluated. The results from the study indicated that adding PVP and nano-TiO2 appropriately in PVDF membranes could be an effective method for better E1and E2 rejection due to adsorption and photocatalytic degradation.

Enhancement of polar crystalline phase formation in transparent PVDF-CaF{sub 2} composite films

Energy Technology Data Exchange (ETDEWEB)

Lee, Sang Goo; Ha, Jong-Wook, E-mail: jongwook@krict.re.kr; Sohn, Eun-Ho; Park, In Jun; Lee, Soo-Bok

2016-12-30

Highlights: • The crystalline phase in transparent PVDF-CaF{sub 2} composite films was investigated. • CaF{sub 2} promoted the formation of polar crystalline phases in PVDF matrix. • Ordered γ-phase was obtained by thermal treatment of as-cast films at the vicinity of its melting temperature. - Abstract: We consider the influence of calcium fluoride (CaF{sub 2}) nanoparticles on the crystalline phase formation of poly(vinylidene fluoride) (PVDF) for the first time. The transparent PVDF-CaF{sub 2} composite films were prepared by casting on PET substrates using N,N-dimethylacetamide (DMAc) as a solvent. It was found that CaF{sub 2} promoted the formation of polar crystalline phase of PVDF in composites, whereas nonpolar α-phase was dominant in the neat PVDF film prepared at the same condition. The portion of polar crystalline phase increased in proportional to the weight fraction of CaF{sub 2} in the composite films up to 10 wt%. Further addition of CaF{sub 2} suppressed completely the α-phase formation. Polar crystalline phase observed in as-cast composite films was a mixture of β- and γ-polymorph structures. It was also shown that much ordered γ-phase could be obtained through thermal treatment of as-cast PVDF-CaF{sub 2} composite film at the temperatures above the melting temperature of the composite films, but below that of γ-phase.

Integrated 3D printing and corona poling process of PVDF piezoelectric films for pressure sensor application

Science.gov (United States)

Kim, Hoejin; Torres, Fernando; Wu, Yanyu; Villagran, Dino; Lin, Yirong; Tseng, Tzu-Liang(Bill

2017-08-01

This paper presents a novel process to fabricate piezoelectric films from polyvinylidene fluoride (PVDF) polymer using integrated fused deposition modeling (FDM) 3D printing and corona poling technique. Corona poling is one of many effective poling processes that has received attention to activate PVDF as a piezoelectric responsive material. The corona poling process occurs when a PVDF polymer is exposed to a high electric field created and controlled through an electrically charged needle and a grid electrode under heating environment. FDM 3D printing has seen extensive progress in fabricating thermoplastic materials and structures, including PVDF. However, post processing techniques such as poling is needed to align the dipoles in order to gain piezoelectric properties. To further simplify the piezoelectric sensors and structures fabrication process, this paper proposes an integrated 3D printing process with corona poling to fabricate piezoelectric PVDF sensors without post poling process. This proposed process, named ‘Integrated 3D Printing and Corona poling process’ (IPC), uses the 3D printer’s nozzle and heating bed as anode and cathode, respectively, to create poling electric fields in a controlled heating environment. The nozzle travels along the programmed path with fixed distance between nozzle tip and sample’s top surface. Simultaneously, the electric field between the nozzle and bottom heating pad promotes the alignment of dipole moment of PVDF molecular chains. The crystalline phase transformation and output current generated by printed samples under different electric fields in this process were characterized by a Fourier transform infrared spectroscopy and through fatigue load frame. It is demonstrated that piezoelectric PVDF films with enhanced β-phase percentage can be fabricated using the IPC process. In addition, mechanical properties of printed PVDF was investigated by tensile testing. It is expected to expand the use of additive

Fluorine incorporation into SnO2 nanoparticles by co-milling with polyvinylidene fluoride

Science.gov (United States)

Senna, Mamoru; Turianicová, Erika; Šepelák, Vladimír; Bruns, Michael; Scholz, Gudrun; Lebedkin, Sergei; Kübel, Christian; Wang, Di; Kaňuchová, Mária; Kaus, Maximilian; Hahn, Horst

2014-04-01

Fluorine was incorporated into SnO2 nanoparticles from polyvinylidene fluoride (PVdF) by co-milling. The incorporation process was triggered by an oxidative partial decomposition of PVdF due to the abstraction of oxygen atoms, and began soon after milling with a simultaneous decrease in the crystallite size of SnO2 from 56 nm to 19 nm, and increase in the lattice strain by a factor 7. Appearance of D and G Raman peaks indicated that the decomposition of PVdF was accompanied by the formation of nanometric carbon species. Decomposing processes of PVdF were accompanied by the continuous change in the states of F, with a decrease of C-F in PVdF and increase in Sn-F. This indicates the gradual incorporation of F into SnO2, by replacing a part of oxygen in the oxide with fluorine. These serial mechanochemical reaction processes were discussed on the basis of X-ray diffractometry, FT-IR, Raman and UV-Vis diffuse reflectance spectroscopy, transmission electron microscopy, F1s, Sn3d and C1s X-ray photoelectron spectroscopy and Auger electron spectra, as well as magic angle spinning NMR spectroscopy of 19F and 119Sn. The present findings serve as an initial stage of incorporating fluorine into SnO2 via a solvent-free solid-state process, toward the rational fabrication of fluorine doped SnO2 powders.

Improving dielectric properties of BaTiO{sub 3}/poly(vinylidene fluoride) composites by employing core-shell structured BaTiO{sub 3}@Poly(methylmethacrylate) and BaTiO{sub 3}@Poly(trifluoroethyl methacrylate) nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Zhang, Xianhong; Zhao, Sidi; Wang, Fang [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Ma, Yuhong, E-mail: mayh@mail.buct.edu.cn [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Beijing Engineering Research Center of Syntheses and Applications of Waterborne Polymers, Beijing University of Chemical Technology, 100029 (China); Wang, Li; Chen, Dong; Zhao, Changwen [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Beijing Engineering Research Center of Syntheses and Applications of Waterborne Polymers, Beijing University of Chemical Technology, 100029 (China); Yang, Wantai, E-mail: yangwt@mail.buct.edu.cn [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Beijing Engineering Research Center of Syntheses and Applications of Waterborne Polymers, Beijing University of Chemical Technology, 100029 (China)

2017-05-01

Highlights: • Core-shell structured BT@PMMA and BT@PTFEMA nanoparticles were synthesized. • The dispersity of BT nanoparticles in PVDF matrix was improved significantly. • Dielectric properties both of BT@PMMA/PVDF and BT@PTFEMA/PVDF composites were improved. • The frequency dependence of dielectric constant attenuation of BT@PTFEMA/PVDF composites was smaller than that of BT@PMMA/PVDF composites. - Abstract: Polymer based dielectric composites were fabricated through incorporation of core-shell structured BaTiO{sub 3} (BT) nanoparticles into PVDF matrix by means of solution blending. Core-shell structured BT nanoparticles with different shell composition and shell thickness were prepared by grafting methacrylate monomer (MMA or TFEMA) onto the surface of BT nanoparticles via surface initiated atom transfer radical polymerization (SI-ATRP). The content of the grafted polymer and the micro-morphology of the core-shell structured BT nanoparticles were investigated by thermo gravimetric analyses (TGA) and transmission electron microscopy (TEM), respectively. The dielectric properties were measured by broadband dielectric spectroscopy. The results showed that high dielectric constant and low dielectric loss are successfully realized in the polymer based composites. Moreover, the type of the grafted polymer and its content had different effect on the dielectric constant. In detail, the attenuation of dielectric constant was 16.6% for BT@PMMA1/PVDF and 10.7% for BT@PMMA2/PVDF composite in the range of 10 Hz to 100 kHz, in which the grafted content of PMMA was 5.5% and 8.0%, respectively. However, the attenuation of dielectric constant was 5.5% for BT@PTFEMA1/PVDF and 4.0% for BT@PTFEMA2/PVDF composite, in which the grafted content of PTFEMA was 1.5% and 2.0%, respectively. These attractive features of BT@PTFEMA/PVDF composites suggested that dielectric ceramic fillers modified with fluorinated polymer can be used to prepare high performance composites, especially

Improving dielectric properties of BaTiO_3/poly(vinylidene fluoride) composites by employing core-shell structured BaTiO_3@Poly(methylmethacrylate) and BaTiO_3@Poly(trifluoroethyl methacrylate) nanoparticles

International Nuclear Information System (INIS)

Zhang, Xianhong; Zhao, Sidi; Wang, Fang; Ma, Yuhong; Wang, Li; Chen, Dong; Zhao, Changwen; Yang, Wantai

2017-01-01

Highlights: • Core-shell structured BT@PMMA and BT@PTFEMA nanoparticles were synthesized. • The dispersity of BT nanoparticles in PVDF matrix was improved significantly. • Dielectric properties both of BT@PMMA/PVDF and BT@PTFEMA/PVDF composites were improved. • The frequency dependence of dielectric constant attenuation of BT@PTFEMA/PVDF composites was smaller than that of BT@PMMA/PVDF composites. - Abstract: Polymer based dielectric composites were fabricated through incorporation of core-shell structured BaTiO_3 (BT) nanoparticles into PVDF matrix by means of solution blending. Core-shell structured BT nanoparticles with different shell composition and shell thickness were prepared by grafting methacrylate monomer (MMA or TFEMA) onto the surface of BT nanoparticles via surface initiated atom transfer radical polymerization (SI-ATRP). The content of the grafted polymer and the micro-morphology of the core-shell structured BT nanoparticles were investigated by thermo gravimetric analyses (TGA) and transmission electron microscopy (TEM), respectively. The dielectric properties were measured by broadband dielectric spectroscopy. The results showed that high dielectric constant and low dielectric loss are successfully realized in the polymer based composites. Moreover, the type of the grafted polymer and its content had different effect on the dielectric constant. In detail, the attenuation of dielectric constant was 16.6% for BT@PMMA1/PVDF and 10.7% for BT@PMMA2/PVDF composite in the range of 10 Hz to 100 kHz, in which the grafted content of PMMA was 5.5% and 8.0%, respectively. However, the attenuation of dielectric constant was 5.5% for BT@PTFEMA1/PVDF and 4.0% for BT@PTFEMA2/PVDF composite, in which the grafted content of PTFEMA was 1.5% and 2.0%, respectively. These attractive features of BT@PTFEMA/PVDF composites suggested that dielectric ceramic fillers modified with fluorinated polymer can be used to prepare high performance composites, especially

Utilization of rice husk ash as silica source for the synthesis of mesoporous silicas and their application to CO2 adsorption through TREN/TEPA grafting

International Nuclear Information System (INIS)

Bhagiyalakshmi, Margandan; Yun, Lee Ji; Anuradha, Ramani; Jang, Hyun Tae

2010-01-01

Mesoporous MCM-41, MCM-48 and SBA-15 were synthesized using Rice husk ash (RHA) as the silica source and their defective Si-OH sites were functionalized by 3-cholropropyltrimethoxysilane (CPTMS) which was subsequently grafted with amine compounds, Tris(2-aminoethyl)amine (TREN) and Tetraethylenepentamine (TEPA). X-ray powder diffraction (XRD) and BET results of the parent mesoporous silica suggested their closeness of structural properties to those obtained from conventional silica sources. CO 2 adsorption of branched amine TREN and straight chain amine TEPA at 25, 50 and 75 deg. C was obtained by Thermogravimetric Analyser (TGA) at atmospheric pressure. TREN grafted mesoporous silica showed 7% of CO 2 adsorption while TEPA grafted mesoporous silicas showed less CO 2 adsorption, which is due to the presence of isolated amine groups in TREN. TREN grafted mesoporous silicas were also observed to be selective towards CO 2 , thermally stable and recyclable. The order of CO 2 adsorption with respect to amount of amine grafting was observed to be MCM-48/TREN > MCM-41/TREN > SBA-15/TREN.

GAS SEPARATION MEMBRANES COMPRISING PERMEABILITY ENHANCING ADDITIVES

NARCIS (Netherlands)

Wessling, Matthias; Sterescu, D.M.; Stamatialis, Dimitrios

2007-01-01

The present invention relates to polymer compositions comprising a (co)polymer comprising (a) an arylene oxide moiety and (b) a dendritic (co)polymer, a hyperbranched (co)polymer or a mixture thereof, and the use of these polymer compositions as membrane materials for the separation of gases. The

Nanocomposites with increased energy density through high aspect ratio PZT nanowires.

Science.gov (United States)

Tang, Haixiong; Lin, Yirong; Andrews, Clark; Sodano, Henry A

2011-01-07

High energy storage plays an important role in the modern electric industry. Herein, we investigated the role of filler aspect ratio in nanocomposites for energy storage. Nanocomposites were synthesized using lead zirconate titanate (PZT) with two different aspect ratio (nanowires, nanorods) fillers at various volume fractions dispersed in a polyvinylidene fluoride (PVDF) matrix. The permittivity constants of composites containing nanowires (NWs) were higher than those with nanorods (NRs) at the same inclusion volume fraction. It was also indicated that the high frequency loss tangent of samples with PZT nanowires was smaller than for those with nanorods, demonstrating the high electrical energy storage efficiency of the PZT NW nanocomposite. The high aspect ratio PZT NWs showed a 77.8% increase in energy density over the lower aspect ratio PZT NRs, under an electric field of 15 kV mm(-1) and 50% volume fraction. The breakdown strength was found to decrease with the increasing volume fraction of PZT NWs, but to only change slightly from a volume fraction of around 20%-50%. The maximum calculated energy density of nanocomposites is as high as 1.158 J cm(-3) at 50% PZT NWs in PVDF. Since the breakdown strength is lower compared to a PVDF copolymer such as poly(vinylidene fluoride-tertrifluoroethylene-terchlorotrifluoroethylene) P(VDF-TreEE-CTFE) and poly(vinylidene fluoride-co-hexafluoropropylene) P(VDF-HFP), the energy density of the nanocomposite could be significantly increased through the use of PZT NWs and a polymer with greater breakdown strength. These results indicate that higher aspect ratio fillers show promising potential to improve the energy density of nanocomposites, leading to the development of advanced capacitors with high energy density.

Measurements of nonlinear optical properties of PVDF/ZnO using Z-scan technique

Energy Technology Data Exchange (ETDEWEB)

Shanshool, Haider Mohammed, E-mail: haidshan62@gmail.com [Ministry of Science and Technology, Baghdad (Iraq); Yahaya, Muhammad [School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Selangor (Malaysia); Yunus, Wan Mahmood Mat [Department of Physics, Faculty of Science, University Putra Malaysia, Serdang (Malaysia); Abdullah, Ibtisam Yahya [Department of Physics, College of Science, University of Mosul, Mosul (Iraq)

2015-10-15

The nonlinear optical properties of ZnO nanoparticles dispersed in poly (vinylidene fluoride) (PVDF) polymer are investigated. PVDF/ZnO nanocomposites were prepared by mixing different concentrations of ZnO nanoparticles, as the filler, with PVDF, as the polymer matrix, using casting method. Acetone was used as a solvent for the polymer. FTIR spectra of the samples were analyzed thus confirming the formation of α and β phases. The absorbance spectra of the samples were obtained, thereby showing high absorption in the UV region. The linear absorption coefficient was calculated. The single-beam Z-scan technique was used to measure the nonlinear refractive index and the nonlinear absorption coefficient of the PVDF/ZnO nanocomposite samples. We observed that the nonlinear refractive index is in the order of 10{sup -13} cm{sup 2}/W with the negative sign, whereas the nonlinear absorption coefficient is in the order of 10{sup -8} cm/W. (author)

Particle localization and hyperuniformity of polymer-grafted nanoparticle materials

Energy Technology Data Exchange (ETDEWEB)

Chremos, Alexandros [Materials Science and Engineering Division, National Institute of Standards and Technology, Gaithersburg, MD (United States); Douglas, Jack F.

2017-05-15

The properties of materials largely reflect the degree and character of the localization of the molecules comprising them so that the study and characterization of particle localization has central significance in both fundamental science and material design. Soft materials are often comprised of deformable molecules and many of their unique properties derive from the distinct nature of particle localization. We study localization in a model material composed of soft particles, hard nanoparticles with grafted layers of polymers, where the molecular characteristics of the grafted layers allow us to ''tune'' the softness of their interactions. Soft particles are particular interesting because spatial localization can occur such that density fluctuations on large length scales are suppressed, while the material is disordered at intermediate length scales; such materials are called ''disordered hyperuniform''. We use molecular dynamics simulation to study a liquid composed of polymer-grafted nanoparticles (GNP), which exhibit a reversible self-assembly into dynamic polymeric GNP structures below a temperature threshold, suggesting a liquid-gel transition. We calculate a number of spatial and temporal correlations and we find a significant suppression of density fluctuations upon cooling at large length scales, making these materials promising for the practical fabrication of ''hyperuniform'' materials. (copyright 2017 by WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Intensifying radiation induced grafting of 4-vinylpyridine/glycidyl methacrylate mixtures onto poly(ethylene-co-tetrafluoroethylene) films using ultrasound

International Nuclear Information System (INIS)

Nasef, Mohamed Mahmoud; Sithambaranathan, Paveswari; Ahmad, Arshad; Abouzari-lotf, Ebrahim

2017-01-01

A new ultrasound-aided method was used to enhance grafting of 4-vinylpyridine (4-VP) and glycidyl methacrylate (GMA) monomers mixtures onto electron beam (EB) irradiated poly(ethylene-co-tetrafluoroethylene) (ETFE) film for the first time. The effects of reaction parameters such as absorbed dose, monomer concentration, reaction time on both of degree of grafting (DG) and grafting efficiency (GE) were investigated under sonication and conventional grafting at similar temperatures. Fourier transform infrared (FTIR) and atomic force microscopy (AFM) were used to monitor the impact of the applied ultrasound on composition and surfaces of the grafted films whereas 1 H-NMR was used to investigate composition of the grafting residues. The ultrasound-aided grafting of 4-VP/GMA was found to enhance both of DG% and GE remarkably. Moreover, it produced grafted ETFE films having smoother surfaces without homopolymer contamination compared to grafted films obtained from conventional grafting. The results of this study suggest that the use of ultrasound is a promising way for intensifying grafting process and improving its economy. - Highlights: • Grafting of 4-VP/GMA onto ETFE films was carried out with the aid of ultrasound. • Degree of grafting was found to be strongly dependent on reaction parameters. • Sonication remarkably enhanced the reaction kinetics and grafting efficiency. • Grafted films with smoother surfaces without homopolymer contamination were obtained. • Ultrasound aided grafting is superior to conventional one and promotes intensification.

Radiation induced graft copolymerization of jute fibre

International Nuclear Information System (INIS)

Al-Siddique, F.R.; Khan, A.U.; Sheikh, R.A.

1983-01-01

Graft copolymerized jute fibres (GCJF) were prepared by γ-ray induced graft copolymerization of various monomers onto bleached and de-waxed jute samples. The effect of γ-ray dose on the tendency of various monomers to form graft co-polymer was studied. It was found that the tendency decreases as follows: methylmethacrylate (MMA)>acrylonitrile (AN)>styrene (STY)>vinylacetate (VA). When the effect of monomer concentration on the formation of graft co-polymer was studied, it was found that a mixture of AN and STY gave a higher amount of grafting than what was observed for STY or AN alone, when used at a comparable concentration. A study on the effect of concentration of methyl alcohol (a swelling agent for jute) on the tendency of the monomers to form graft co-polymer showed that although there is no effect when only AN is used, an appreciable effect is observed if AN is mixed with STY. In the later case the tendency of graft co-polymerization increases with the increase of CH 3 OH concentration. It was further observed that the increase of CH 3 OH also has a positive influence on MMA to form graft co-polymer in the range of 40-90% CH 3 OH. The affinity of GCJF towards moisture has been found to decrease with the increase of polymer loading onto jute. The presence of swelling agents during graft copolymer formation was also found to decrease the affinity of GCJF towards moisture. (author)

Mechanical Degradation of Graphite/PVDF Composite Electrodes: A Model-Experimental Study

Energy Technology Data Exchange (ETDEWEB)

Takahashi, K; Higa, K; Mair, S; Chintapalli, M; Balsara, N; Srinivasan, V

2015-12-11

Mechanical failure modes of a graphite/polyvinylidene difluoride (PVDF) composite electrode for lithium-ion batteries were investigated by combining realistic stress-stain tests and mathematical model predictions. Samples of PVDF mixed with conductive additive were prepared in a similar way to graphite electrodes and tested while submerged in electrolyte solution. Young's modulus and tensile strength values of wet samples were found to be approximately one-fifth and one-half of those measured for dry samples. Simulations of graphite particles surrounded by binder layers given the measured material property values suggest that the particles are unlikely to experience mechanical damage during cycling, but that the fate of the surrounding composite of PVDF and conductive additive depends completely upon the conditions under which its mechanical properties were obtained. Simulations using realistic property values produced results that were consistent with earlier experimental observations.

Synergistic promotion of polar phase crystallization of PVDF by ionic liquid with PEG segment

Science.gov (United States)

Xu, Pei; Fu, Weijia; Cui, Zhaopei; Ding, Yunsheng

2018-06-01

To investigate the effect of imidazolium ionic liquid with poly(ethylene glycol) segment (IL) on the polar phase crystallization behavior of poly(vinylidene fluoride) (PVDF), a series of PVDF/IL composites were prepared using solution-cast method. The crystallization peak temperature of PVDF composites and the growth speed of samples decrease with increasing of IL. The >CF2 groups in amorphous region are retained and >CF2 groups in crystalline region are liberated by the PEG long soft segments of IL. The intensity of peaks represented as α phase reduces, moreover polar phase content increases with increasing of IL. The interaction between the >CF2 and the imidazolium cation can induce the polar phase, and the interaction between the >CF2 and PEG soft segment can strengthen polar crystalline induction. PVDF/12IL composite can form big γ spherulite circled by β phase.

Effect of Polyamide 6 on Crystalline Structure of Polymer in PVDF-Nanoclay Nanocomposite

Directory of Open Access Journals (Sweden)

Ali Akbar Yousefi

2012-12-01

Full Text Available The  effect  of  nanocaly  on  crystalline  structure  of  poly(vinylidene  fuoride, PVDF, and the morphology of the resulting nano-composite were investigated using  different  characterization  techniques.  The  presence  of  3wt%  Cloisite 30B in PVDF matrix results in 11 fold increase in the percentage of beta crystalline content of the polymer. This was found to be attributed to the epitaxial effect of the clay  surface. The  beta  crystalline  content  of  the  pure  polymer  (6% was  raised  to 68% in the composite. Addition of 5wt% polyamide 6 (PA6 improved dispersion of nanoclay which led to augmentation of the viscosity and displacement of the crossover frequency of the compatibilized composite towards lower frequencies. However, due to stronger affnity of the PA6 towards organically modifed clay the epitaxial effect of  the  clay on  crystalline  structure of PVDF was  totally  eliminated. The  reduction of  viscosity  in  incompatibilized  nanocomposite was  attributed  to  reduced  number of PVDF chain entanglements  in  the presence of nanoclay. Meanwhile,  increase  in viscosity and displacement of crossover  frequency  towards  lower  frequencies were attributed to formation of clay-PA nanoparticles and PVDF-polyamide 6 interactions. It is expected that the presence of polyamide 6 promotes the formation of oriented-beta crystals in PVDF, which in turn improves the piezoelectric properties of the polymer.

Biodegradability of poly(3-hydroxybutyrate) film grafted with vinyl acetate: Effect of grafting and saponification

Science.gov (United States)

Wada, Yuki; Seko, Noriaki; Nagasawa, Naotsugu; Tamada, Masao; Kasuya, Ken-ichi; Mitomo, Hiroshi

2007-06-01

Radiation-induced graft polymerization of vinyl acetate (VAc) onto poly(3-hydroxybutyrate) (PHB) film was carried out. At a degree of grafting higher than 5%, the grafted films (PHB-g-VAc) completely lost the enzymatic degradability that is characteristic of PHB due to the grafted VAc covering the surface of the PHB film. However, the biodegradability of the PHB-g-VAc films was recovered when the films were saponified in alkali solution under optimum conditions. Graft chains of the PHB-g-VAc film reacted selectively to become biodegradable polyvinyl alcohol (PVA). The biodegradability of the saponified PHB-g-VAc film increased rapidly with time.

Biodegradability of poly(3-hydroxybutyrate) film grafted with vinyl acetate: Effect of grafting and saponification

International Nuclear Information System (INIS)

Wada, Yuki; Seko, Noriaki; Nagasawa, Naotsugu; Tamada, Masao; Kasuya, Ken-ichi; Mitomo, Hiroshi

2007-01-01

Radiation-induced graft polymerization of vinyl acetate (VAc) onto poly(3-hydroxybutyrate) (PHB) film was carried out. At a degree of grafting higher than 5%, the grafted films (PHB-g-VAc) completely lost the enzymatic degradability that is characteristic of PHB due to the grafted VAc covering the surface of the PHB film. However, the biodegradability of the PHB-g-VAc films was recovered when the films were saponified in alkali solution under optimum conditions. Graft chains of the PHB-g-VAc film reacted selectively to become biodegradable polyvinyl alcohol (PVA). The biodegradability of the saponified PHB-g-VAc film increased rapidly with time

A facile TiO{sub 2}/PVDF composite membrane synthesis and their application in water purification

Energy Technology Data Exchange (ETDEWEB)

Zhang, Wei, E-mail: wei.zhang@unisa.edu.au; Zhang, Yiming; Fan, Rong; Lewis, Rosmala [University of South Australia, Centre for Water Management and Reuse (Australia)

2016-01-15

In this work, we have demonstrated a facile wet chemical method to synthesise TiO{sub 2}/PVDF composite membranes as alternative water purification method to traditional polymer-based membrane. For the first time, hydrothermally grown TiO{sub 2} nanofibers under alkali conditions were successfully inserted into PVDF membranes matrix. The structure, permeability and anti-fouling performance of as-prepared PVDF/TiO{sub 2} composite membranes were studied systematically. The TiO{sub 2}/PVDF composite membranes prepared in this work promise great potential uses in water purification applications as microfiltration membranes due to its excellent physical/chemical resistance, anti-fouling and mechanical properties.

Graft copolymers of polypropylene films. 1. radiation induced grafting of mixed monomers. Vol. 3

International Nuclear Information System (INIS)

El-Salmawi, K.M.; El-Naggar, A.M.; Said, H.M.; Zahran, A.H.

1996-01-01

Radiation graft copolymerization of co monomer mixtures of acrylic acid (AAC), and styrene (S) onto polypropylene (PP) film by mutual method has been investigated. The effects of different factors that may affect the grafting yield such as inhibitor concentration (Mohr's salt), solvent composition (MeOH and H 2 O), radiation dose and dose rate were considered. It was found that the role of Mohr's salt is very effective when the ratio of AAC in the co monomer mixtures was at lower values. However, the addition of 1.25 Wt% of Mohr's salt reduced the homo polymer formation and enhances the grafting process. Graft copolymerization in presence of solvent mixture composed of methanol and water was found to afford higher grafting than in pure methanol regardless of the composition of the co monomer mixture used. However, the highest degree of grafting was obtained at a solvent composition of 20% H 2 O:80%MeOH and a co monomer mixture of 20%AAC:80%sty. An attempt was made to determine each PAAC and PS fractions in the total graft yield obtained. Two methods of analysis based on using the reactivity ratios reported in literature, elemental analysis and IR spectroscopy. The determination of poly (acrylic acid) and polystyrene fractions by elemental analysis is believed more accurate than these by reactivity ratio. The precise results obtained by elemental analysis with respect to the chemical structure of known polymer prepared under identical conditions. The results obtained by IR measurements go well with that obtained with the reactivity ratio methods. 5 figs., 3 tabs

Fabrication, polarization, and characterization of PVDF matrix composites for integrated structural load sensing

International Nuclear Information System (INIS)

Haghiashtiani, Ghazaleh; Greminger, Michael A

2015-01-01

The focus of this work is to evaluate a new carbon fiber reinforced composite structure with integrated sensing capabilities. In this composite structure, the typical matrix material used for carbon fiber reinforced composites is replaced with the thermoplastic polyvinylidene difluoride (PVDF). Since PVDF has piezoelectric properties, it enables the structure to be used for integrated load sensing. In addition, the electrical conductivity property of the carbon fabric is harnessed to form the electrodes of the integrated sensor. In order to prevent the carbon fiber electrodes from shorting to each other, a thin Kevlar fabric layer is placed between the two carbon fiber electrode layers as a dielectric. The optimal polarization parameters were determined using a design of experiments approach. Once polarized, the samples were then used in compression and tensile tests to determine the effective d 33 and d 31 piezoelectric coefficients. The degree of polarization of the PVDF material was determined by relating the effective d 33 coefficient of the composite to the achieved d 33 of the PVDF component of the composite using a closed form expression. Using this approach, it was shown that optimal polarization of the composite material results in a PVDF component d 33 of 3.2 pC N −1 . Moreover, the Young’s modulus of the composite structure has been characterized. (paper)

Properties of grafted polymer metal complexes as ion exchangers and its electrical conductivity

International Nuclear Information System (INIS)

El-Arnaouty, M.B.; Abdel Ghaffar, A.M.; Eid, M.

2011-01-01

The polyelectrolyte has been prepared as a potential proton exchanger polymer by grafting of acrylic acid/acrylamide and acrylic acid/acrylonitrile comonomer onto low density polyethylene film via gamma radiation. The influence of grafting percent on the electrical conductivity was studied. The resulting polymers were then characterized by evaluating their physico-chemical properties such as ion exchange capacity, and electrical conductivity as a function of grafting yield. The grafted films at different compositions was characterized by FTIR, TGA and SEM. The ion exchange capacity (IEC) of the grafted film at grafting % (191) and monomer concentration ratio 50:50 for (LDPE-g-AAc/AAm) was found to be more than that for (LDPE-g-AAc/AN). The electrical conductivity was found to be greatly affected by the comonomer composition where it increased as the degree of grafting increased for all grafted films. After alkaline treatment with 3% KOH, the electrical conductivity of the grafted films found to be increased. The presence of potassium as counter ion maximized the electrical conductivity of the grafted films. The electrical conductivity of Cu-membrane complexes was higher than that of both Co and Ni complexes. The electrical conductivity increases by increasing both Cu ions content and temperature

Molecular Dynamics Study of the Separation Behavior at the Interface between PVDF Binder and Copper Current Collector

Directory of Open Access Journals (Sweden)

Seungjun Lee

2016-01-01

Full Text Available In Li-ion batteries, the mechanical strengths at the interfaces of binder/particle and binder/current collector play an important role in maintaining the mechanical integrity of the composite electrode. In this work, the separation behaviors between polyvinylidene fluoride (PVDF binders and copper current collectors are studied in the opening and sliding modes using molecular dynamics (MD simulations. The simulation shows that the separation occurs inside the PVDF rather than at the interface due to the strong adhesion between PVDF and copper. This fracture behavior is different from the behavior of the PVDF/graphite basal plane that shows a clear separation at the interface. The results suggest that the adhesion strength of the PVDF/copper is stronger than that of the PVDF/graphite basal plane. The methodology used in MD simulation can directly evaluate the adhesion strength at the interfaces of various materials between binders, substrates, and particles at the atomic scales. The proposed method can therefore provide a guideline for the design of the electrode in order to enhance the mechanical integrity for better battery performance.

Surface grafting of poly(ethylene glycol) onto poly(acrylamide-co-vinyl amine) cross-linked films under mild conditions.

Science.gov (United States)

Yamamoto, Y; Sefton, M V

1998-01-01

Poly(ethylene glycol) (PEG) was grafted onto poly(acrylamide-co-vinyl amine) (poly(AM-co-VA)) film using tresylated PEG (TPEG) at 37 degrees C in aqueous buffers (pH 7.4) with a view to surface-modifying microencapsulated mammalian cells. Poly(AM-co-VA) film was synthesized by Hofmann degradation of a cross-linked poly(acrylamide) film. Conversion to vinyl amine on the surface of the film was approximately 50%, but bulk conversion was not observed; surface specificity was thought to be the result of cleavage of aminated polymer chains at the surface due to chain scission. Reaction between primary amine and TPEG gave a graft yield of 2 mol% (based on XPS) with respect to available surface amine groups, equivalent to 54 mol% ethylene oxide based on monomer units. Physical adsorption of non-activated polymer was done under identical conditions as a control and the difference in oxygen content was significant compared to TPEG. The type of buffer agent and buffer concentration did not influence graft yields. This graft reaction, which was completed in as little as 2 h was considered to be mild enough to be used for a surface modification of microcapsules containing cells without affecting their viability. Such a surface modification technique may prove to be a useful means of enhancing the biocompatibility of microcapsules (or any tissue engineering construct) even after cell encapsulation or seeding.

Nanoclay-Directed Structure and Morphology in PVDF Electrospun Membranes

Directory of Open Access Journals (Sweden)

Kyunghwan Yoon

2014-01-01

Full Text Available The incorporation of organically modified Lucentite nanoclay dramatically modifies the structure and morphology of the PVDF electrospun fibers. In a molecular level, the nanoclay preferentially stabilizes the all-trans conformation of the polymer chain, promoting an α to β transformation of the crystalline phase. The piezoelectric properties of the β-phase carry great promise for energy harvest applications. At a larger scale, the nanoclay facilitates the formation of highly uniform, bead-free fibers. Such an effect can be attributed to the enhanced conductivity and viscoelasticity of the PVDF-clay suspension. The homogenous distribution of the directionally aligned nanoclays imparts advanced mechanical properties to the nanofibers.

Interfacial durability and electrical properties of CNT or ITO/PVDF nanocomposites for self-sensor and micro actuator applications

International Nuclear Information System (INIS)

Park, Joung-Man; Gu, Ga-Young; Wang, Zuo-Jia; Kwon, Dong-Jun; DeVries, K. Lawrence

2013-01-01

Interfacial durability and electrical properties of CNT (carbon nanotube) or ITO (indium tin oxide) coated PVDF (poly(vinylidene fluoride)) nanocomposites were investigated for self-sensor and micro-actuator applications. The electrical resistivity of nanocomposites and the durability of interfacial adhesion were measured using a four points method during cyclic fatigue loading. Although the CNT/PVDF nanocomposites exhibited lower electrical resistivity due to the inherently low resistivity of CNT, both composite types showed good self-sensing performance. The durability of the adhesion at the interface was also good for both CNT and ITO/PVDF nanocomposites. Static contact angle, surface energy, work of adhesion, and spreading coefficient between either CNT or ITO and PVDF were determined as checks to verify the durability of the interfacial adhesion. The actuation performance of CNT or ITO coated PVDF specimens was determined through measurements of the induced displacement using a laser displacement sensor, while both the frequency and voltage were changed. The displacement of these actuated nanocomposites increased with increasing voltage and decreased with increasing frequency. CNT/PVDF nanocomposites exhibited better performance as self-sensors and micro-actuators than did ITO/PVDF nanocomposites.

Monitoring of composite structures using a network of integrated PVDF film transducers

International Nuclear Information System (INIS)

Guzmán, Enrique; Cugnoni, Joël; Gmür, Thomas

2015-01-01

Aiming to reduce costs, polyvinylidene difluoride (PVDF) film patches are an emerging alternative to more classic piezoelectric technologies, like ceramic patches, as transducers to measure local deformation in many structural applications. This choice is supported by advantages such as the low weight and mechanical flexibility of PVDF, making this polymer suitable for embedding inside full scale polymer based composite structures. Piezoelectric transducer patches can be used as actuators to dynamically excite full-scale composite structures, and as sensors to measure the strain. The main objective of this paper is to verify that the PVDF transducers can provide exploitable signals in the context of structural health monitoring. In order to do so, two aspects of the design of transducer network are investigated: the optimization of the sensor network, for which the effective independence method is proposed, and the use of operational modal analysis (OMA), since it is a simple method to extract the natural frequencies of a structure from a time series. The results of the analysis are compared to a reference set issued from experimental modal analysis (EMA), a simple, well-known, classic method, which is carried out using accelerometers and an impact hammer. By statistical means, it is shown that there is no significant difference between the two methods, and an optimized PVDF transducer network combined with OMA can perform the dynamic analysis of a structure as well as a classic EMA setup would do. This leads the way to the use of low-cost PVDF embedded transducer networks for robust composite material characterization. (paper)

Meniscal allograft transplantation. Part 1: systematic review of graft biology, graft shrinkage, graft extrusion, graft sizing, and graft fixation.

Science.gov (United States)

Samitier, Gonzalo; Alentorn-Geli, Eduard; Taylor, Dean C; Rill, Brian; Lock, Terrence; Moutzouros, Vasilius; Kolowich, Patricia

2015-01-01

To provide a systematic review of the literature regarding five topics in meniscal allograft transplantation: graft biology, shrinkage, extrusion, sizing, and fixation. A systematic literature search was conducted using the PubMed (MEDLINE), ScienceDirect, and EBSCO-CINAHL databases. Articles were classified only in one topic, but information contained could be reported into other topics. Information was classified according to type of study (animal, in vitro human, and in vivo human) and level of evidence (for in vivo human studies). Sixty-two studies were finally included: 30 biology, 3 graft shrinkage, 11 graft extrusion, 17 graft size, and 6 graft fixation (some studies were categorized in more than one topic). These studies corresponded to 22 animal studies, 22 in vitro human studies, and 23 in vivo human studies (7 level II, 10 level III, and 6 level IV). The principal conclusions were as follows: (a) Donor cells decrease after MAT and grafts are repopulated with host cells form synovium; (b) graft preservation alters collagen network (deep freezing) and causes cell apoptosis with loss of viable cells (cryopreservation); (c) graft shrinkage occurs mainly in lyophilized and gamma-irradiated grafts (less with cryopreservation); (d) graft extrusion is common but has no clinical/functional implications; (e) overall, MRI is not superior to plain radiograph for graft sizing; (f) graft width size matching is more important than length size matching; (g) height appears to be the most important factor influencing meniscal size; (h) bone fixation better restores contact mechanics than suture fixation, but there are no differences for pullout strength or functional results; and (i) suture fixation has more risk of graft extrusion compared to bone fixation. Systematic review of level II-IV studies, Level IV.

Surface modification of poly(styrene-b-(ethylene-co-butylene)-b-styrene) elastomer via photo-initiated graft polymerization of poly(ethylene glycol)

Energy Technology Data Exchange (ETDEWEB)

Li Xiaomeng [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Luan Shifang, E-mail: sfluan@ciac.jl.cn [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Yang Huawei; Shi Hengchong; Zhao Jie; Jin Jing [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Yin Jinghua, E-mail: yinjh@ciac.jl.cn [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Stagnaro, Paola [Istituto per Io Studio delle Macromolecole, Consiglio Nazionale delle Ricerche, Via de Marini 6, 16149 Genova (Italy)

2012-01-15

Poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) copolymer biomedical elastomer was covalently grafted with poly(ethylene glycol) methyl ether methacrylate (PEGMA) via a photo-initiated graft polymerization technique. The surface graft polymerization of SEBS with PEGMA was verified by ATR-FTIR and XPS. Effect of graft polymerization parameters, i.e., monomer concentration, UV irradiation time and initiator concentration on the grafting density was investigated. Comparing with the virgin SEBS film, the PEGMA-modified SEBS film presented an enhanced wettability and a larger surface energy. Besides, the surface grafting of PEGMA imparted excellent anti-platelet adhesion and anti-protein adsorption to the SEBS surface.

Optimization Of PVDF-TrFE Processing Conditions For The Fabrication Of Organic MEMS Resonators.

Science.gov (United States)

Ducrot, Pierre-Henri; Dufour, Isabelle; Ayela, Cédric

2016-01-21

This paper reports a systematic optimization of processing conditions of PVDF-TrFE piezoelectric thin films, used as integrated transducers in organic MEMS resonators. Indeed, despite data on electromechanical properties of PVDF found in the literature, optimized processing conditions that lead to these properties remain only partially described. In this work, a rigorous optimization of parameters enabling state-of-the-art piezoelectric properties of PVDF-TrFE thin films has been performed via the evaluation of the actuation performance of MEMS resonators. Conditions such as annealing duration, poling field and poling duration have been optimized and repeatability of the process has been demonstrated.

Synthesis and crystalline properties of CdS incorporated polyvinylidene fluoride (PVDF) composite film

Science.gov (United States)

Patel, Arunendra Kumar; Sunder, Aishwarya; Mishra, Shweta; Bajpai, Rakesh

2018-05-01

This paper gives an insight on the synthesis and crystalline properties of Polyvinylidene Fluoride (PVDF) (host matrix) composites impregnated with Cadmium Sulphide (CdS) using Dimethyl formamide (DMF) as the base, prepared by the well known solvent casting technique. The effect of doping concentration of CdS in to the PVDF matrix was studied using X-ray diffraction technique. The structural properties like crystallinity Cr, interplanar distance d, average size of the crystalline region (D), and average inter crystalline separation (R) have been estimated for the developed composite. The crystallinity index, crystallite size and inter crystalline separation is increasing with increase in the concentration of CdS in to the PVDF matrix while the interplanar distance d is decreasing.

Graft copolymers of polypropylene films. 1. radiation induced grafting of mixed monomers. Vol. 3

Energy Technology Data Exchange (ETDEWEB)

El-Salmawi, K M; El-Naggar, A M; Said, H M; Zahran, A H [Radiation Chemistry Department, National Center for Radiation Research and Technology, Atomic Energy Authority, Cairo, (Egypt)

1996-03-01

Radiation graft copolymerization of co monomer mixtures of acrylic acid (AAC), and styrene (S) onto polypropylene (PP) film by mutual method has been investigated. The effects of different factors that may affect the grafting yield such as inhibitor concentration (Mohr`s salt), solvent composition (MeOH and H{sub 2} O), radiation dose and dose rate were considered. It was found that the role of Mohr`s salt is very effective when the ratio of AAC in the co monomer mixtures was at lower values. However, the addition of 1.25 Wt% of Mohr`s salt reduced the homo polymer formation and enhances the grafting process. Graft copolymerization in presence of solvent mixture composed of methanol and water was found to afford higher grafting than in pure methanol regardless of the composition of the co monomer mixture used. However, the highest degree of grafting was obtained at a solvent composition of 20% H{sub 2} O:80%MeOH and a co monomer mixture of 20%AAC:80%sty. An attempt was made to determine each PAAC and PS fractions in the total graft yield obtained. Two methods of analysis based on using the reactivity ratios reported in literature, elemental analysis and IR spectroscopy. The determination of poly (acrylic acid) and polystyrene fractions by elemental analysis is believed more accurate than these by reactivity ratio. The precise results obtained by elemental analysis with respect to the chemical structure of known polymer prepared under identical conditions. The results obtained by IR measurements go well with that obtained with the reactivity ratio methods. 5 figs., 3 tabs.

In-situcross-linked PVDF membranes with enhanced mechanical durability for vacuum membrane distillation

KAUST Repository

Zuo, Jian; Chung, Neal Tai-Shung

2016-01-01

A novel and effective one-step method has been demonstrated to fabricate cross-linked polyvinylidene fluoride (PVDF) membranes with better mechanical properties and flux for seawater desalination via vacuum membrane distillation (VMD). This method involves the addition of two functional nonsolvent additives; namely, water and ethylenediamine (EDA), into the polymer casting solution. The former acts as a pore forming agent, while the latter performs as a cross-linking inducer. The incorporation of water tends to increase membrane flux via increasing porosity and pore size but sacrifices membrane mechanical properties. Conversely, the presence of EDA enhances membrane mechanical properties through in-situ cross-linking reaction. Therefore, by synergistically combining the effects of both functional additives, the resultant PVDF membranes have shown good MD performance and mechanical properties simultaneously. The parameters that affect the cross-link reaction and membrane mechanical properties such as reaction duration and EDA concentration have been systematically studied. The membranes cast from an optimal reaction condition comprising 0.8 wt % EDA and 3-hour reaction not only shows a 40% enhancement in membrane Young's Modulus compared to the one without EDA but also achieves a good VMD flux of 43.6 L/m2-h at 60°C. This study may open up a totally new approach to design next-generation high performance MD membranes. © 2016 American Institute of Chemical Engineers AIChE J, 62: 4013–4022, 2016

In-situcross-linked PVDF membranes with enhanced mechanical durability for vacuum membrane distillation

KAUST Repository

Zuo, Jian

2016-05-12

A novel and effective one-step method has been demonstrated to fabricate cross-linked polyvinylidene fluoride (PVDF) membranes with better mechanical properties and flux for seawater desalination via vacuum membrane distillation (VMD). This method involves the addition of two functional nonsolvent additives; namely, water and ethylenediamine (EDA), into the polymer casting solution. The former acts as a pore forming agent, while the latter performs as a cross-linking inducer. The incorporation of water tends to increase membrane flux via increasing porosity and pore size but sacrifices membrane mechanical properties. Conversely, the presence of EDA enhances membrane mechanical properties through in-situ cross-linking reaction. Therefore, by synergistically combining the effects of both functional additives, the resultant PVDF membranes have shown good MD performance and mechanical properties simultaneously. The parameters that affect the cross-link reaction and membrane mechanical properties such as reaction duration and EDA concentration have been systematically studied. The membranes cast from an optimal reaction condition comprising 0.8 wt % EDA and 3-hour reaction not only shows a 40% enhancement in membrane Young\\'s Modulus compared to the one without EDA but also achieves a good VMD flux of 43.6 L/m2-h at 60°C. This study may open up a totally new approach to design next-generation high performance MD membranes. © 2016 American Institute of Chemical Engineers AIChE J, 62: 4013–4022, 2016

Efficient visible light photocatalytic NO{sub x} removal with cationic Ag clusters-grafted (BiO){sub 2}CO{sub 3} hierarchical superstructures

Energy Technology Data Exchange (ETDEWEB)

Feng, Xin [Chongqing Key Laboratory of Catalysis and Functional Organic Molecules, College of Environment and Resources, Engineering Research Center for Waste Oil Recovery Technology and Equipment of Ministry of Education, College of Environment and Resources, Chongqing Technology and Business University, Chongqing 40067 (China); Zhang, Wendong [Department of Scientific Research Management, Chongqing Normal University, Chongqing 401331 (China); Deng, Hua [State Key Joint Laboratory of Environment Simulation and Pollution Control, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); Ni, Zilin [Department of Scientific Research Management, Chongqing Normal University, Chongqing 401331 (China); Dong, Fan, E-mail: dfctbu@126.com [Chongqing Key Laboratory of Catalysis and Functional Organic Molecules, College of Environment and Resources, Engineering Research Center for Waste Oil Recovery Technology and Equipment of Ministry of Education, College of Environment and Resources, Chongqing Technology and Business University, Chongqing 40067 (China); Zhang, Yuxin, E-mail: zhangyuxin@cqu.edu.cn [College of Materials Science and Engineering, National Key Laboratory of Fundamental Science of Micro/Nano-Devices and System Technology, Chongqing University, Chongqing 400044 (China)

2017-01-15

Graphical abstract: The cationic Ag clusters-grafted (BiO){sub 2}CO{sub 3} hierarchical superstructures exhibits highly enhanced visible light photocatalytic air purification through an interfacial charge transfer process induced by Ag clusters. - Highlights: • Microstructural optimization and surface cluster-grafting were firstly combined. • Cationic Ag clusters were grafted on the surface of (BiO){sub 2}CO{sub 3} superstructures. • The Ag clusters-grafted BHS displayed enhanced visible light photocatalysis. • Direct interfacial charge transfer (IFCT) from BHS to Ag clusters was proposed. • The charge transfer process and the dominant reactive species were revealed. - Abstract: A facile method was developed to graft cationic Ag clusters on (BiO){sub 2}CO{sub 3} hierarchical superstructures (BHS) surface to improve their visible light activity. Significantly, the resultant Ag clusters-grafted BHS displayed a highly enhanced visible light photocatalytic performance for NOx removal due to the direct interfacial charge transfer (IFCT) from BHS to Ag clusters. The chemical and coordination state of the cationic Ag clusters was determined with the extended X-ray absorption fine structure (EXAFS) and a theoretical structure model was proposed for this unique Ag clusters. The charge transfer process and the dominant reactive species (·OH) were revealed on the basis of electron spin resonance (ESR) trapping. A new photocatalysis mechanism of Ag clusters-grafted BHS under visible light involving IFCT process was uncovered. In addition, the cationic Ag clusters-grafted BHS also demonstrated high photochemical and structural stability under repeated photocatalysis runs. The perspective of enhancing photocatalysis through combination of microstructural optimization and IFCT could provide a new avenue for the developing efficient visible light photocatalysts.

Effect of annealing temperatures on the morphology and structural properties of PVDF/MgO nanocomposites thin films

Science.gov (United States)

Rozana, M. D.; Arshad, A. N.; Wahid, M. H. M.; Habibah, Z.; Sarip, M. N.; Rusop, M.

2018-05-01

This study investigates the effect of annealing on the topography, morphology and crystal phases of poly(vinylideneflouride)/Magnesium Oxide (MgO) nanocomposites thin films via AFM, FESEM and ATR-FTIR. The nanocomposites thin films were annealed at temperatures ranging from 70°C to 170°C. The annealed PVDF/MgO nanocomposites thin films were then cooled at room temperature before removal from the oven. This is to restructure the crystal lattice and to reduce imperfection for the PVDF/MgO nanocomposites thin films. PVDF/MgO nanocomposites thin films with annealing temperatures of 70°C, 90°C and 110°C showed uniform distribution of MgO nanoparticles, relatively low average surface roughness and no visible of defects. High application of annealing temperature on PVDF/MgO nanocomposites thin films caused tear-like defects on the thin films surface as observed by FESEM. The PVDF/MgO nanocomposites thin films annealed at 70°C was found to be a favourable film to be utilized in this study due to its enhanced β-crystalites of PVDF as evident in ATR-FTIR spectra.

Magnetoelectric investigations on poly (vinylidene fluoride)/CoFe2O4 flexible electrospun membranes

Science.gov (United States)

Durgaprasad, P.; Hemalatha, J.

2018-02-01

Flexible and free standing magnetoelectric polymer nanocomposite electrospun membranes, which exhibit both ferroelectric and magnetic orderings simultaneously, are fabricated. CoFe2O4 nanoparticles of different weight percentages are embedded as fillers in poly (vinylidene fluoride) (PVDF) matrix. The percentage of electroactive β phase is analysed using XRD and FTIR studies. Investigations on the effect of filler on the structural, functional, morphological properties are discussed. CoFe2O4 content in PVDF plays a main role in controlling the α and β phase conformations and makes significant effect on the ferroelectric and ferromagnetic properties of PVDF/CoFe2O4 membranes. The domain switching behaviour of these ferroelectric membranes is confirmed through DC-EFM studies. In addition to the coexistence of ferroelectric and ferromagnetic orderings, the cross coupling between them have been proved.

Evaluation of PVDF/MWCNT - ZRO{sub 2} nanocomposites for X-Rays attenuation

Energy Technology Data Exchange (ETDEWEB)

Pereira, Esther L.M.; Oliveira, Arno H., E-mail: esther_machado@outlook.com.br, E-mail: heeren@nuclear.ufmg.br [Universidade Federal de Minas Gerais (CCTN/UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear; Batista, Adriana S.M., E-mail: adriananuclear@yahoo.com.br [Departamento de Anatomia e Imagem (IMA), Belo Horizonte, MG (Brazil); Ribeiro, Fabíola A.S.; Santos, Adelina P.; Faria, Luiz O., E-mail: adelina@cdtn.br, E-mail: farialo@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

2017-07-01

Recently, polymer-based nanocomposites filled with zirconium oxide (ZrO{sub 2}) nanoparticles have been suggested to be used in radiology procedures as X-rays attenuators. On the other hand, multi walled carbon nanotubes (MWCNT) has been reported to have enhanced X-rays attenuation features, when compared to other materials. In this work polymer-based nanocomposites made of a poly(vinylidene fluoride) [PVDF] homopolymer co-filled with MWCNT and zirconia (ZrO{sub 2}) were prepared, in order to investigate them for radiation shielding purposes. The PVDF matrix was added to 1.3% ZrO{sub 2} and the MWCNT in three different proportions: 0.33%, 0.66% and 1% of MWCNT.The arrangement between these materials causes new properties to be introduced to the constituents due to morphological modifications or electronic interactions between them, resulting in a nanocomposite of higher properties. The radiation shielding characterization was performed by using the X-ray beam of a XRD equipment. Photons with energies of 6.5 keV, 17.5 keV and 22.1 keV, corresponding to the anodes of cobalt, molybdenum and silver respectively, were used. The results are discussed in terms of the attenuation percentage of the nanocomposites produced in relation to the energy of the exposed radiation beam and varying the thickness of the samples. A comparison with cataloged aluminum data is also performed. (author)

PETMA-g-PETMA-b-PS 'palm tree' graft copolymer: A new polymeric architecture obtained via RAFT and ROP process

International Nuclear Information System (INIS)

Soares, Paula P.; Silva, Eduardo de O. da; Petzhold, Cesar L.

2009-01-01

Block copolymer with pendant thiirane moiety PETMA-b-PS is the base for a new class of 'palm tree' graft copolymers, which can show interesting properties. ETMA can be polymerized through ring opening polymerization with Lewis bases as initiator, e.g., Br- and tertiary amines. We used this reaction as a way to graft a copolymer PETMA-b-PS possessing 5% of ETMA unities, with chains having poly(propylene sulfide), obtained by graft from method. Produced materials were characterized through H1 NMR, SEC and DSC. (author)

Preparation and characterization of a novel PVDF ultrafiltration membrane by blending with TiO_2-HNTs nanocomposites

International Nuclear Information System (INIS)

Zeng, Guangyong; He, Yi; Yu, Zongxue; Zhan, Yingqing; Ma, Lan; Zhang, Lei

2016-01-01

Highlights: • A novel TiO_2-HNTs/PVDF ultrafiltration membrane was prepared. • TiO_2 dispersed well in membrane matrix by loading on the surface of HNTs. • The hydrophilicity of membrane was improved with the addition of TiO_2-HNTs. • TiO_2-HNTs/PVDF membranes showed good antifouling performance. - Abstract: Novel polyvinylidene fluoride (PVDF) ultrafiltration membranes were prepared by blending with different contents of titanium dioxide-halloysite nanotubes (TiO_2-HNTs) composites into the PVDF matrix. The effects of TiO_2-HNTs content on the membrane performances, such as hydrophilicity, rejection ratio and antifouling properties were investigated in detail. X-ray diffraction (XRD), thermo-gravimetric analyzer (TGA) and scanning electron microscope (SEM) analyses showed that TiO_2 was loaded on the surface of HNTs successfully and homogeneously by sol-gel method. The morphologies and microstructure of the membranes were characterized by SEM and atomic force microscopy (AFM). The contact angle (CA) tests indicated that the hydrophilicity of membranes was significantly increased with the addition of TiO_2-HNTs. The pure water flux of 3%TiO_2-HNTs/PVDF was increased by 264.8% and 35.6%, respectively, compared with pure PVDF membrane and 3%TiO_2/PVDF membrane, although the rejection of bovine serum albumin (BSA) was slightly decreased. More importantly, TiO_2-HNTs/PVDF membrane exhibited an excellent anti-fouling performance, which was attributed to the hydrophobic contaminants being resisted by hydrophilic nanoparticles. It can be expected that this work may provide some references to solve the dispersion of nanoparticle in the membrane and improve the anti-fouling performance of membrane in the field of wastewater treatment.

Synthesis and characterization of starch-g-poly(vinyl acetate-co-butyl acrylate) bio-based adhesive for wood application.

Science.gov (United States)

Zia-Ud-Din; Chen, Lei; Ullah, Ikram; Wang, Peng Kai; Javaid, Allah Bakhsh; Hu, Chun; Zhang, Mengchao; Ahamd, Ishtiaq; Xiong, Hanguo; Wang, Zhenjiong

2018-07-15

Enhancing the performance of wood adhesive is important for its industrial applications. Accordingly, we designed and demonstrated the use of two co-monomers vinyl acetate (VAc) and butyl acrylate (BA) for promoting the graft copolymerization while improving the bonding performance of wood adhesive. The results showed that the addition of co-monomers in the ratio of VAc/BA 6:4 (v/v, volume basis of VAc) could improve the shear strength to 6.68MPa and 3.32MPa in dry and wet states, respectively. 1 H-nuclear magnetic resonance ( 1 H NMR) and fourier transform infrared spectroscopy (FT-IR) analysis revealed successful graft copolymerization reaction while the morphologies were observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Furthermore, the grafting reaction and thermal stabilities of wood adhesive were analyzed by X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA). The results showed that the properties of wood adhesive could improve dramatically by using two co-monomers VAc and BA during the graft copolymerization reaction. Copyright © 2018 Elsevier B.V. All rights reserved.

Chemical modification of polyaniline by N-grafting of polystyrenic chains synthesized via nitroxide-mediated polymerization

International Nuclear Information System (INIS)

Hatamzadeh, Maryam; Mahyar, Ali; Jaymand, Mehdi

2012-01-01

This study aims to explore an effective route for the preparation of conductive N-substituted polyaniline (PANI) by the incorporation of brominated poly(styrene-co-p-methylstyrene) onto the emeraldine form of polyaniline. For this purpose, at first, poly(styrene-co-p-methylstyrene) was synthesized via nitroxide-mediated polymerization (NMP), and then, N-bromosuccinimide was used as brominating agent to obtain a copolymer with bromine. Thereafter, deprotonated polyaniline was reacted with brominated poly(styrene-co-p-methylstyrene) to prepare the poly(styrene-co-p-methylstyrene)-graft-polyaniline [(PSt-co-PMSt)-g-PANI] terpolymer through N-grafting reaction. The terpolymer was characterized by Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Optical properties of (PSt-co-PMSt)-g-PANI in the undoped and doped states were obtained by ultraviolet-visible spectroscopy (UV-Vis), and electrical conductivity at room temperature was measured using samples in which the conductive materials was sandwiched between two Ni electrodes. Moreover, electroactivity of the synthesized terpolymer was verified under cyclic voltammetric conditions on the surface of the working glassy carbon electrode (GCE). The solubility of (PSt-co-PMSt)-g-PANI terpolymer was examined in common organic solvents, such as, tetrahydrofuran (THF), chloroform and xylene. (author)

Fabrication of thermo-responsive PNIPAAm-g-ETFE for cell culture dishes by pre-irradiation grafting

Science.gov (United States)

Yamahara, Yumi; Nagasawa, Naotsugu; Taguchi, Mitsumasa; Oshima, Akihiro; Washio, Masakazu

2018-01-01

Thermo-responsive templates for the cell cultivation based on Poly(tetrafluoroethylene-co-ethylene) (ETFE) were fabricated by pre-irradiation grafting of N-isoproplyacrylamide (NIPAAm) monomer by electron beam (EB) irradiation under nitrogen gas atmosphere at room temperature, and their characteristic properties were studied. The detachment of cultured HeLa cells from fabricated thermo-responsive templates were attempted. Furthermore, the reaction mechanism is proposed using ESR spectroscopy and FT-IR spectroscopy. It is confirmed that the cultured HeLa cells were detached from fabricated thermo-responsive templates at 20 °C. Water contact angle analysis indicated that obtained templates had thermo-response around 30 °C. It is suggested that the grafted polymer chains would mainly react with peroxy radicals (-CF2-CF(OO･)-) on tetrafluoroethylene unit in ETFE.

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

International Nuclear Information System (INIS)

Nikham

2004-01-01

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

Nanocomposites for Improved Physical Durability of Porous PVDF Membranes

Science.gov (United States)

Lai, Chi Yan; Groth, Andrew; Gray, Stephen; Duke, Mikel

2014-01-01

Current commercial polymer membranes have shown high performance and durability in water treatment, converting poor quality waters to higher quality suitable for drinking, agriculture and recycling. However, to extend the treatment into more challenging water sources containing abrasive particles, micro and ultrafiltration membranes with enhanced physical durability are highly desirable. This review summarises the current limits of the existing polymeric membranes to treat harsh water sources, followed by the development of nanocomposite poly(vinylidene fluoride) (PVDF) membranes for improved physical durability. Various types of nanofillers including nanoparticles, carbon nanotubes (CNT) and nanoclays were evaluated for their effect on flux, fouling resistance, mechanical strength and abrasion resistance on PVDF membranes. The mechanisms of abrasive wear and how the more durable materials provide resistance was also explored. PMID:24957121

Mechanical behavior of styrene grafted PVC films by electron beam irradiation

International Nuclear Information System (INIS)

Cardoso, Jessica R.; Moura, Eduardo; Somessari, Elisabeth S.R.; Silveira, Carlos G.; Paes, Helio A.; Souza, Carlos A.; Manzoli, Jose E.; Geraldo, Aurea B.C.

2011-01-01

The polyvinyl chloride (PVC) is a technological and low cost polymer, however it presents high sensitivity to high energy irradiation because of the weakness of carbon-chloride bond face to carbon-carbon and carbon-hydrogen bonds. Grafting is a type of co-polymerization process that can allow it an increase of mechanical characteristics. The aim of this work is to evaluate the mechanical properties of styrene grafted PVC by electron beam irradiation using mutual and pre-irradiation methods to verify the mechanical resistance changes of obtained product whether grafting process is applied from non-irradiated or from pre-irradiated substrates. The irradiation procedures were performed in atmosphere air or inert atmosphere and the irradiation conditions comprised doses from 10 kGy to 100 kGy and dose rates of 2.2 kGy/s and 22.4 kGy/s. The styrene grafted samples were analyzed by gravimetry to determinate the grafting yield; the final values have been averaged from a series of three measurements. The Mid-A TR-FTIR was the spectrophotometer technique used for qualitative/semi-quantitative analysis of grafted samples. The Young's module and tensile strength of pre-irradiated and grafted PVC samples at both methods were measured at a Lloyd LXR tensile tester at a cross-head speed of 10.00 mm/min. We observed the decrease of Young's module and tensile strength with the increase of absorbed dose at pre-irradiated PVC samples. These mechanical parameters results are discussed. (author)

Radiolytic Synthesis of Pt-Ru Catalysts Based on Functional Polymer-Grafted MWNT and Their Catalytic Efficiency for CO and MeOH

Directory of Open Access Journals (Sweden)

Dae-Soo Yang

2011-01-01

Full Text Available Pt-Ru catalysts based on functional polymer-grafted MWNT (Pt-Ru@FP-MWNT were prepared by radiolytic deposition of Pt-Ru nanoparticles on functional polymer-grafted multiwalled carbon nanotube (FP-MWNT. Three different types of functional polymers, poly(acrylic acid (PAAc, poly(methacrylic acid (PMAc, and poly(vinylphenyl boronic acid (PVPBAc, were grafted on the MWNT surface by radiation-induced graft polymerization (RIGP. Then, Pt-Ru nanoparticles were deposited onto the FP-MWNT supports by the reduction of metal ions using γ-irradiation to obtain Pt-Ru@FP-MWNT catalysts. The Pt-Ru@FP-MWNT catalysts were then characterized by XRD, XPS, TEM ,and elemental analysis. The catalytic efficiency of Pt-Ru@FP-MWNT catalyst was examined for CO stripping and MeOH oxidation for use in a direct methanol fuel cell (DMFC. The Pt-Ru@PVPBAc-MWNT catalyst shows enhanced activity for electro-oxidation of CO and MeOH oxidation over that of the commercial E-TEK catalyst.

Radiation grafting on natural films

Science.gov (United States)

Lacroix, M.; Khan, R.; Senna, M.; Sharmin, N.; Salmieri, S.; Safrany, A.

2014-01-01

Different methods of polymer grafting using gamma irradiation are reported in the present study for the preparation of newly functionalized biodegradable films, and some important properties related to their mechanical and barrier properties are described. Biodegradable films composed of zein and poly(vinyl alcohol) (PVA) were gamma-irradiated in presence of different ratios of acrylic acid (AAc) monomer for compatibilization purpose. Resulting grafted films (zein/PVA-g-AAc) had their puncture strength (PS=37-40 N mm-1) and puncture deformation (PD=6.5-9.8 mm) improved for 30% and 50% PVA in blend, with 5% AAc under 20 kGy. Methylcellulose (MC)-based films were irradiated in the presence of 2-hydroxyethyl methacrylate (HEMA) or silane, in order to determine the effect of monomer grafting on the mechanical properties of films. It was found that grafted films (MC-g-HEMA and MC-g-silane) using 35% monomer performed higher mechanical properties with PS values of 282-296 N mm-1 and PD of 5.0-5.5 mm under 10 kGy. Compatibilized polycaprolactone (PCL)/chitosan composites were developed via grafting silane in chitosan films. Resulting trilayer grafted composite film (PCL/chitosan-g-silane/PCL) presented superior tensile strength (TS=22 MPa) via possible improvement of interfacial adhesion (PCL/chitosan) when using 25% silane under 10 kGy. Finally, MC-based films containing crystalline nanocellulose (CNC) as a filling agent were prepared and irradiated in presence of trimethylolpropane trimethacrylate (TMPTMA) as a grafted plasticizer. Grafted films (MC-g-TMPTMA) presented superior mechanical properties with a TS of 47.9 MPa and a tensile modulus (TM) of 1792 MPa, possibly due to high yield formation of radicals to promote TMPTMA grafting during irradiation. The addition of CNC led to an additional improvement of the barrier properties, with a significant 25% reduction of water vapor permeability (WVP) of grafted films.

Positive temperature coefficient of magnetic anisotropy in polyvinylidene fluoride (PVDF)-based magnetic composites

OpenAIRE

Liu, Yiwei; Wang, Baomin; Zhan, Qingfeng; Tang, Zhenhua; Yang, Huali; Liu, Gang; Zuo, Zhenghu; Zhang, Xiaoshan; Xie, Yali; Zhu, Xiaojian; Chen, Bin; Wang, Junling; Li, Run-Wei

2014-01-01

The magnetic anisotropy is decreased with increasing temperature in normal magnetic materials, which is harmful to the thermal stability of magnetic devices. Here, we report the realization of positive temperature coefficient of magnetic anisotropy in a novel composite combining β-phase polyvinylidene fluoride (PVDF) with magnetostrictive materials (magnetostrictive film/PVDF bilayer structure). We ascribe the enhanced magnetic anisotropy of the magnetic film at elevated temperature to the st...

Grafting of styrene onto poly(vinylidene fluoride) films by gamma irradiation; Enxertia de estireno em filmes de poli(fluoreto de vinilideno) induzida por irradiacao gama

Energy Technology Data Exchange (ETDEWEB)

Ferreira, H.P.; Souza, C.P. de; Parra, D.F.; Lugao, A.B., E-mail: hp.ferreira@yahoo.com.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Quimica e Meio Ambiente

2010-07-01

Radiation induced grafting of styrene onto poly(vinylidene fluoride) (PVDF) was studied owing to the crescent interest in use of grafted films to produce membranes with ion exchange capability. A Cobalt-60 source was used, with doses of 5 and 10 kGy, at dose rate of 5 kGy.h{sup -1}, at room temperature, inert atmosphere and according to the simultaneous method. Solutions of styrene/toluene (1:1, v/v) and styrene/N,N-dimethylformamide (DMF) (1:1, v/v) were used. The films were characterized by FT-IR spectroscopy (Infrared Spectroscopy), Differential Scanning Calorimetry (DSC), Thermogravimetric Measurement (TG) and the degree of grafting (DOG) were calculated gravimetrically. Results shown that in studied conditions, DMF allow greatest DOG than toluene and that increasing the irradiation dose correspond an increase in DOG. Infrared and thermal analyses confirmed the presence in the grafted polymers. (author)

Correlation Study of PVDF Membrane Morphology with Protein Adsorption: Quantitative Analysis by FTIR/ATR Technique

Science.gov (United States)

Ideris, N.; Ahmad, A. L.; Ooi, B. S.; Low, S. C.

2018-05-01

Microporous PVDF membranes were used as protein capture matrices in immunoassays. Because the most common labels in immunoassays were detected based on the colour change, an understanding of how protein concentration varies on different PVDF surfaces was needed. Herein, the correlation between the membrane pore size and protein adsorption was systematically investigated. Five different PVDF membrane morphologies were prepared and FTIR/ATR was employed to accurately quantify the surface protein concentration on membranes with small pore sizes. SigmaPlot® was used to find a suitable curve fit for protein adsorption and membrane pore size, with a high correlation coefficient, R2, of 0.9971.

Desenvolvimento de um acelerometro em PVDF e sua aplicação a sistemas vibratorios

OpenAIRE

Carlos Minor Tomiyoshi

1994-01-01

Resumo:O nível de voltagem gerado pelo acelerômetro em PVDF foi utilizado como parâmetro referencial para verificação da conformidade de sistemas mecânicos, de modo simples e direto. 0 método desenvolvido foi baseado em um novo tipo de acelerômetro, de concepção original, composto por duas películas piezelétricas em PVDF (Polyvinylidene Fluoride) e massa líquida (mercúrio) como elemento excitador. O acelerômetro em PVDF funcionou como um componente binário (on/off), para indicar se o nível de...

Radiodegradation process in PVDF with different molecular weight

International Nuclear Information System (INIS)

Silva, L.; Batista, A.S.M.; Nascimento, J.P.; Furtado, C.A.; Faria, L.O.

2017-01-01

Poly(vinylidene fluoride) (PVDF) is a semi-crystalline polymer with several industrial applications due to its mechanical, ferroelectric and biocompatibility properties. Due to the particularity of some of its applications this polymer is exposed to high energy radiation, for example in the aerospace industry and with biomaterial, in sterilization processes. In this sense it is of interest studies that evaluate the radiodegradation of this material, as a way to predict its mechanical behavior after processes of exposure to gamma radiation. In this study the radioresistance of PVDF with different molecular weights is evaluated, considering that large molecular chains can provide greater resistance than smaller chains. Method: PVDF samples with different molecular weights were produced by the solvent dilution process. They were irradiated with gamma doses of 100, 300, 500, 1000 and 2000 kGy with a source of cobalt in the Laboratório de Irradiação Gama (LIG) of the Centro de Desenvolvimento da Tecnologia Nuclear (CDTN). FTIR, UV-Vis, DSC and XRD analyzes were used to evaluate the induced radiodegradation processes immediately after irradiation and one month later. Results: The FTIR and UV-Vis analyzes showed formation of unsaturations in the polymer chains. The DSC technique showed a drop in the crystalline fraction of the polymer confirmed by the XRD technique. Conclusion: Post-irradiation sample evaluations are discussed in terms of the effect of high energy ionizing radiation on polymeric mate-rials for industrial and biomedical use for safety in quality assurance and performance in service. (author)

Radiodegradation process in PVDF with different molecular weight

Energy Technology Data Exchange (ETDEWEB)

Silva, L.; Batista, A.S.M., E-mail: adriananuclear@yahoo.com.br [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil); Nascimento, J.P.; Furtado, C.A.; Faria, L.O. [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

2017-07-01

Poly(vinylidene fluoride) (PVDF) is a semi-crystalline polymer with several industrial applications due to its mechanical, ferroelectric and biocompatibility properties. Due to the particularity of some of its applications this polymer is exposed to high energy radiation, for example in the aerospace industry and with biomaterial, in sterilization processes. In this sense it is of interest studies that evaluate the radiodegradation of this material, as a way to predict its mechanical behavior after processes of exposure to gamma radiation. In this study the radioresistance of PVDF with different molecular weights is evaluated, considering that large molecular chains can provide greater resistance than smaller chains. Method: PVDF samples with different molecular weights were produced by the solvent dilution process. They were irradiated with gamma doses of 100, 300, 500, 1000 and 2000 kGy with a source of cobalt in the Laboratório de Irradiação Gama (LIG) of the Centro de Desenvolvimento da Tecnologia Nuclear (CDTN). FTIR, UV-Vis, DSC and XRD analyzes were used to evaluate the induced radiodegradation processes immediately after irradiation and one month later. Results: The FTIR and UV-Vis analyzes showed formation of unsaturations in the polymer chains. The DSC technique showed a drop in the crystalline fraction of the polymer confirmed by the XRD technique. Conclusion: Post-irradiation sample evaluations are discussed in terms of the effect of high energy ionizing radiation on polymeric mate-rials for industrial and biomedical use for safety in quality assurance and performance in service. (author)

Preparation and characterization of a novel PVDF ultrafiltration membrane by blending with TiO{sub 2}-HNTs nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Zeng, Guangyong [College of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); Oil & Gas Field Applied Chemistry Key Laboratory of Sichuan Province, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); He, Yi, E-mail: heyi@swpu.edu.cn [College of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); Oil & Gas Field Applied Chemistry Key Laboratory of Sichuan Province, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); State Key Laboratory of Oil & Gas Reservoir Geology and Exploitation, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); Yu, Zongxue; Zhan, Yingqing; Ma, Lan [College of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); Oil & Gas Field Applied Chemistry Key Laboratory of Sichuan Province, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); Zhang, Lei, E-mail: zgc166929@sohu.com [College of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu, Sichuan 610500 (China); Oil & Gas Field Applied Chemistry Key Laboratory of Sichuan Province, Southwest Petroleum University, Chengdu, Sichuan 610500 (China)

2016-05-15

Highlights: • A novel TiO{sub 2}-HNTs/PVDF ultrafiltration membrane was prepared. • TiO{sub 2} dispersed well in membrane matrix by loading on the surface of HNTs. • The hydrophilicity of membrane was improved with the addition of TiO{sub 2}-HNTs. • TiO{sub 2}-HNTs/PVDF membranes showed good antifouling performance. - Abstract: Novel polyvinylidene fluoride (PVDF) ultrafiltration membranes were prepared by blending with different contents of titanium dioxide-halloysite nanotubes (TiO{sub 2}-HNTs) composites into the PVDF matrix. The effects of TiO{sub 2}-HNTs content on the membrane performances, such as hydrophilicity, rejection ratio and antifouling properties were investigated in detail. X-ray diffraction (XRD), thermo-gravimetric analyzer (TGA) and scanning electron microscope (SEM) analyses showed that TiO{sub 2} was loaded on the surface of HNTs successfully and homogeneously by sol-gel method. The morphologies and microstructure of the membranes were characterized by SEM and atomic force microscopy (AFM). The contact angle (CA) tests indicated that the hydrophilicity of membranes was significantly increased with the addition of TiO{sub 2}-HNTs. The pure water flux of 3%TiO{sub 2}-HNTs/PVDF was increased by 264.8% and 35.6%, respectively, compared with pure PVDF membrane and 3%TiO{sub 2}/PVDF membrane, although the rejection of bovine serum albumin (BSA) was slightly decreased. More importantly, TiO{sub 2}-HNTs/PVDF membrane exhibited an excellent anti-fouling performance, which was attributed to the hydrophobic contaminants being resisted by hydrophilic nanoparticles. It can be expected that this work may provide some references to solve the dispersion of nanoparticle in the membrane and improve the anti-fouling performance of membrane in the field of wastewater treatment.

Study on grafting glycidyl methacrylate onto HDPE membranes by pre-irradiation graft copolymerization

International Nuclear Information System (INIS)

Tong Long; Zu Jianhua; Liu Xinwen; Sun Guisheng; Yu Chunhui

2006-01-01

Glycidyl methacrylate (GMA) was grafted onto HDPE membranes by pre-irradiation method with 1.8 MeV E-beam and a kind of membranes having reactive epoxy groups was successfully synthesized. Effects of monomer concentration, reaction temperature and time and irradiation dose on the grafting yield were studied. Composition, thermo-property and surface morphology of the grafted membranes were studied by FTIR, DSC and Tapping-mode AFM, respectively. The FTIR measurements proved the synthesized copolymer is HDPE-g-GMA. The DSC results indicated the grafted HDPE's melting temperature (T m ) and heat of fusion (ΔH f ( HDPE) ) which was reduced with increasing grafting yield. The AFM images indicated that surface of the HDPE-g-GMA membranes was rougher than the virgin HDPE. (authors)

Patterned, highly stretchable and conductive nanofibrous PANI/PVDF strain sensors based on electrospinning and in situ polymerization

Science.gov (United States)

Yu, Gui-Feng; Yan, Xu; Yu, Miao; Jia, Meng-Yang; Pan, Wei; He, Xiao-Xiao; Han, Wen-Peng; Zhang, Zhi-Ming; Yu, Liang-Min; Long, Yun-Ze

2016-01-01

A facile fabrication strategy via electrospinning and followed by in situ polymerization to fabricate a patterned, highly stretchable, and conductive polyaniline/poly(vinylidene fluoride) (PANI/PVDF) nanofibrous membrane is reported. Owing to the patterned structure, the nanofibrous PANI/PVDF strain sensor can detect a strain up to 110%, for comparison, which is 2.6 times higher than the common nonwoven PANI/PVDF mat and much larger than the previously reported values (usually less than 15%). Meanwhile, the conductivity of the patterned strain sensor shows a linear response to the applied strain in a wide range from 0% to about 85%. Additionally, the patterned PANI/PVDF strain sensor can completely recover to its original electrical and mechanical values within a strain range of more than 22%, and exhibits good durability over 10 000 folding-unfolding tests. Furthermore, the strain sensor also can be used to detect finger motion. The results demonstrate promising application of the patterned nanofibrous membrane in flexible electronic fields.A facile fabrication strategy via electrospinning and followed by in situ polymerization to fabricate a patterned, highly stretchable, and conductive polyaniline/poly(vinylidene fluoride) (PANI/PVDF) nanofibrous membrane is reported. Owing to the patterned structure, the nanofibrous PANI/PVDF strain sensor can detect a strain up to 110%, for comparison, which is 2.6 times higher than the common nonwoven PANI/PVDF mat and much larger than the previously reported values (usually less than 15%). Meanwhile, the conductivity of the patterned strain sensor shows a linear response to the applied strain in a wide range from 0% to about 85%. Additionally, the patterned PANI/PVDF strain sensor can completely recover to its original electrical and mechanical values within a strain range of more than 22%, and exhibits good durability over 10 000 folding-unfolding tests. Furthermore, the strain sensor also can be used to detect finger

Starch-g-Poly-(N, N-dimethyl acrylamide-co-acrylic acid): an efficient Cr (VI) ion binder.

Science.gov (United States)

Kolya, Haradhan; Roy, Anirban; Tripathy, Tridib

2015-01-01

Synthesis of Starch-g-(Poly N, N-dimethylacrylamide-co-acrylic acid) was carried out by solution polymerization technique using potassium perdisulfate (K(2)S(2)O(8)) as the initiator. The graft copolymer was characterized by measuring molecular weight, using size exclusion chromatography (SEC), FTIR spectroscopy and X-ray diffraction (XRD) studies. The synthetic graft copolymer was used for removal of hexavalent chromium ion [Cr (VI)] from its aqueous solution. Various operating variables affecting the metal sorption such as, the amount of adsorbent, solution pH, contact time, temperature and the Cr (VI) solution concentration were extensively investigated. FTIR and UV-VIS spectroscopy, cyclic voltammetry (CV) were employed to study the metal complexation. The adsorption data could be well described by the pseudo-second-order and Langmuir isotherm model which indicate a chemisorption process. Calculation of the various thermodynamic parameters for the adsorption was also done. The negative value of free energy change (ΔG°) indicates the spontaneous nature of the adsorption. Copyright © 2014 Elsevier B.V. All rights reserved.

In situ ZnO nanowire growth to promote the PVDF piezo phase and the ZnO-PVDF hybrid self-rectified nanogenerator as a touch sensor.

Science.gov (United States)

Li, Zetang; Zhang, Xu; Li, Guanghe

2014-03-28

A PVDF-ZnO nanowires (NWs) hybrid generator (PZHG) was designed. A simple, cost effective method to produce the PVDF β phase by nano force is introduced. With the ZnO NWs growing, the in situ nano extension force promotes the phase change. A theoretical analysis of the ZnO NWs acting as a self-rectifier of the nano generator is established. The ZnO NWs acted as a self-adjustment diode to control the current output of the PZHG by piezo-electric and semi-conductive effects. Based on the self-controllability of the piezoelectric output, three kinds of finger touching are distinguished by the output performances of the PZHG, which is applicable to an LCD touch pad.

Facile synthesis of nano cauliflower and nano broccoli like hierarchical superhydrophobic composite coating using PVDF/carbon soot particles via gelation technique.

Science.gov (United States)

Sahoo, Bichitra Nanda; Balasubramanian, Kandasubramanian

2014-12-15

We have elucidated a cost effective fabrication technique to produce superhydrophobic polyvinylidene fluoride (PVDF/DMF/candle soot particle and PVDF/DMF/camphor soot particle composite) porous materials. The water repellent dry composite was formed by the interaction of non-solvent (methanol) into PVDF/carbon soot particles suspension in N,N-dimethylformamide (DMF). It is seen that longer quenching time effectively changes the surface morphology of dry composites. The nano broccoli like hierarchical microstructure with micro or nano scaled roughen surface was obtained for PVDF/DMF/camphor soot particle, which reveals water contact angle of 172° with roll off angle of 2°. However, composite coating of PVDF/DMF/candle soot particle shows nano cauliflower like hierarchical, which illustrates water contact angle of 169° with roll off angle of 3°. To elucidate the enhancement of water repellent property of PVDF composites, we further divulge the evolution mechanism of nano cauliflower and nano broccoli structure. In order to evaluate the water contact angle of PVDF composites, surface diffusion of water inside the pores is investigated. Furthermore, the addition of small amount of carbon soot particles in composite not only provides the crystallization of PVDF, but also leads to dramatical amendment of surface morphology which increases the surface texture and roughness for superhydrophobicity. Copyright © 2014 Elsevier Inc. All rights reserved.

Lead free Bi0.5Na0.5TiO3 (BNT) and polyvinylidene fluoride (PVDF) based nanocomposite for energy storage applications

Science.gov (United States)

Pradhan, Lagen Kumar; Pandey, Rabichandra; Kumar, Sunil; Kar, Manoranjan

2018-05-01

Novel ceramic-polymer nanocomposites have great potential for electrical energy storage applications due to its high energy storage density. In the present work, BNT and PVDF based flexible polymer nanocomposites (BNT-PVDF) with different volume fraction (ϕ = 0, 5, 10, 15) were fabricated by solution casting method. Enhancement in beta phase of PVDF polymer matrix with the volume fraction (ϕ = 5, 10, 15) of BNT has been confirmed by X-ray diffraction (XRD) technique as well as Fourier transform infrared (FTIR) spectroscopy analysis. The enhancement of β phase increases as compared to (α) phases with volume fraction (ϕ) of nanofiller (BNT) in the matrix (PVDF) due to internal stress at the interface as well as structural modification of PVDF matrix. BNT-PVDF nanocomposites (with ϕ=10) showed a high dielectric constant (ɛr ≈ 78) relative to pure PVDF (ɛr ≈ 10) at 100 Hz. In addition to this, it exhibits relaxor type ferroelectric behavior with energy storage efficiency up to 77% for the volume fraction (ϕ) of 10.

Synergism of Electrospinning and Nano-alumina Trihydrate on the Polymorphism, Crystallinity and Piezoelectric Performance of PVDF Nanofibers

Science.gov (United States)

Khalifa, Mohammed; Deeksha, B.; Mahendran, Arunjunairaj; Anandhan, S.

2018-03-01

Poly(vinlylidene fluoride) (PVDF) is known for its electroactive phases, which can be nucleated by incorporating nanoparticles into PVDF to enhance its piezoelectric performance. In this study, the synergistic effect of electrospinning and nano alumina trihydrate (ATH) filler was used to enhance the electroactive β phase of PVDF. Electrospun nanofibers of PVDF/ATH nanocomposite (PANCF) were synthesized with different loadings of ATH. The presence of ATH enhances the surface charges of the electrospun droplets, leading to thinner fibers. The highest β-phase content was found to be 70.1% for PANCF with 10% ATH. The piezoelectric performance of the nanofiber mats was studied using an indigenous setup. The highest voltage output of 840 mV was produced by PANCF with 10% ATH. These nanofibers could be a promising material in the field of sensors, actuators and energy-harvesting applications.

Mechanical behavior of styrene grafted PVC films by electron beam irradiation

Energy Technology Data Exchange (ETDEWEB)

Cardoso, Jessica R.; Moura, Eduardo; Somessari, Elisabeth S.R.; Silveira, Carlos G.; Paes, Helio A.; Souza, Carlos A.; Manzoli, Jose E.; Geraldo, Aurea B.C., E-mail: ageraldo@ipen.br, E-mail: jmanzoli@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2011-07-01

The polyvinyl chloride (PVC) is a technological and low cost polymer, however it presents high sensitivity to high energy irradiation because of the weakness of carbon-chloride bond face to carbon-carbon and carbon-hydrogen bonds. Grafting is a type of co-polymerization process that can allow it an increase of mechanical characteristics. The aim of this work is to evaluate the mechanical properties of styrene grafted PVC by electron beam irradiation using mutual and pre-irradiation methods to verify the mechanical resistance changes of obtained product whether grafting process is applied from non-irradiated or from pre-irradiated substrates. The irradiation procedures were performed in atmosphere air or inert atmosphere and the irradiation conditions comprised doses from 10 kGy to 100 kGy and dose rates of 2.2 kGy/s and 22.4 kGy/s. The styrene grafted samples were analyzed by gravimetry to determinate the grafting yield; the final values have been averaged from a series of three measurements. The Mid-A TR-FTIR was the spectrophotometer technique used for qualitative/semi-quantitative analysis of grafted samples. The Young's module and tensile strength of pre-irradiated and grafted PVC samples at both methods were measured at a Lloyd LXR tensile tester at a cross-head speed of 10.00 mm/min. We observed the decrease of Young's module and tensile strength with the increase of absorbed dose at pre-irradiated PVC samples. These mechanical parameters results are discussed. (author)

Methodological development and characterization of welded joints in Poly (vinylidene fluoride) (PVDF); Desenvolvimento metodologico e caracterizacao de juntas soldadas de PVDF

Energy Technology Data Exchange (ETDEWEB)

Cedrola, S.M.L.; Costa, M.F. da; Pasqualino, I.P., E-mail: samanta@metalmat.ufrj.b [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil)

2010-07-01

Pipelines are of great concern in the transport sector of oil and gas industries, mainly due to the natural internal aging process caused by contact with the different transported fluids. Installation of polymeric pipes called liners is a good option for rehabilitation of long segments of deteriorated pipelines. Among the potential materials for such application is Poly (vinylidene fluoride) (PVDF). Meanwhile the installation process cannot be carried out in one single step and the polymeric pipe must be cut in sections that are welded during the installation process. In this research welding methodology was studied aiming to optimize welding conditions and the mechanical properties of the joined materials. The first step was processing the PVDF via compression molding on different conditions. Then, the sample was cut and butt-welded. Welding parameters such as, time control, temperature and contact pressure were studied. Afterwards, the stress-strain properties of the welded material was evaluated and physical characterization was carried by x-ray diffraction (DRX). (author)

Halloysite nanotubes grafted hyperbranched (co)polymers via surface-initiated self-condensing vinyl (co)polymerization

International Nuclear Information System (INIS)

Mu Bin; Zhao Mingfei; Liu Peng

2008-01-01

Halloysite nanotubes (HNTs) grafted hyperbranched polymers were prepared by the self-condensing vinyl polymerization (SCVP) of 2-((bromoacetyl)oxy)ethyl acrylate (BAEA) and the self-condensing vinyl copolymerization of n-butyl acrylate (BA) and BAEA with BAEA as inimer (AB*) respectively, from the surfaces of the 2-bromoisobutyric acid modified halloysite nanotubes (HNTs-Br) via atom transfer radical polymerization (ATRP) technique. The halloysite nanotubes grafted hyperbranched polymer (HNTs-HP) and the halloysite nanotubes grafted hyperbranched copolymer (HNTs-HCP) were characterized by elemental analysis (EA), Fourier transform infrared (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and transmission electron microscope (TEM). The grafted hyperbranched polymers were characterized with Nuclear magnetic resonance (NMR) and the molecular ratio between the inimer AB* and BA in the grafted hyperbranched copolymers was found to be 3:2, calculated from the TGA and EA results

Halloysite nanotubes grafted hyperbranched (co)polymers via surface-initiated self-condensing vinyl (co)polymerization

Energy Technology Data Exchange (ETDEWEB)

Mu Bin; Zhao Mingfei; Liu Peng [Lanzhou University, State Key Laboratory of Applied Organic Chemistry and Institute of Polymer Science and Engineering, College of Chemistry and Chemical Engineering (China)], E-mail: pliu@lzu.edu.cn

2008-05-15

Halloysite nanotubes (HNTs) grafted hyperbranched polymers were prepared by the self-condensing vinyl polymerization (SCVP) of 2-((bromoacetyl)oxy)ethyl acrylate (BAEA) and the self-condensing vinyl copolymerization of n-butyl acrylate (BA) and BAEA with BAEA as inimer (AB*) respectively, from the surfaces of the 2-bromoisobutyric acid modified halloysite nanotubes (HNTs-Br) via atom transfer radical polymerization (ATRP) technique. The halloysite nanotubes grafted hyperbranched polymer (HNTs-HP) and the halloysite nanotubes grafted hyperbranched copolymer (HNTs-HCP) were characterized by elemental analysis (EA), Fourier transform infrared (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and transmission electron microscope (TEM). The grafted hyperbranched polymers were characterized with Nuclear magnetic resonance (NMR) and the molecular ratio between the inimer AB* and BA in the grafted hyperbranched copolymers was found to be 3:2, calculated from the TGA and EA results.

Synthesis and characterization of organometallic copolymers of acrylic acid g-polyethylene, with Mo, Fe, Co, Zn and Ni

International Nuclear Information System (INIS)

Dorantes R, G.L.

1997-01-01

In this study, the preparation of a series of low density polyethylenes grafted with acrylic acid is presented. The grafting reactions were initiated by different doses of γ radiation; it was observed that grafting increased with the doses of radiation. The prepared copolymers were coordinated with different metals, as Mo, Fe, Co, Zn and Ni. The amount of metal supported on the polymer was determined by atomic absorption. Infrared spectroscopy and thermogravimetric analysis confirmed the metal chelation on the graft copolymer. The film surfaces were observed by scanning electron microscopy. positron annihilation spectroscopy revealed a decrease on the free volume in the low density polyethylene after the grafting with acrylic acid. (Author)

Evaluation of Optimal Pore Size of (3-Aminopropyltriethoxysilane Grafted MCM-41 for Improved CO2 Adsorption

Directory of Open Access Journals (Sweden)

Zhilin Liu

2015-01-01

Full Text Available An array of new MCM-41 with substantially larger average pore diameters was synthesized through adding 1,3,5-trimethylbenzene (TMB as the swelling agent to explore the effect of pore size on final adsorbent properties. The pore expanded MCM-41 was also grafted with (3-Aminopropyltriethoxysilane (APTES to determine the optimal pore size for CO2 adsorption. The pore-expanded mesoporous MCM-41s showed relatively less structural regularity but significant increments of pore diameter (4.64 to 7.50 nm; the fraction of mesopore volume also illustrated an increase. The adsorption heat values were correlated with the order of the adsorption capacities for pore expanded MCM-41s. After amine functionalization, the adsorption capacities and heat values showed a significant increase. APTES-grafted pore-expanded MCM-41s depicted a high potential for CO2 capture regardless of the major drawback of the high energy required for regeneration.

Effect of roll hot press temperature on crystallite size of PVDF film

Energy Technology Data Exchange (ETDEWEB)

Hartono, Ambran, E-mail: ambranhartono@yahoo.com; Sanjaya, Edi [Departement of Physics Faculty of Science and Technology, Islamic State University Syarif Hidayatullah , Jl. Juanda 95 Ciputat Jakarta (Indonesia); Djamal, Mitra; Satira, Suparno; Bahar, Herman [Theoretical High Energy Physics and Instrumentation Group Research, Faculty Mathematics and Natural Sciences, Institut Teknologi Bandung, Jl. Ganesa 10 Bandung (Indonesia); Ramli [Departement of Physics, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Jl.Prof. Hamka, Padang 25131 (Indonesia)

2014-03-24

Fabrication PVDF films have been made using Hot Roll Press. Preparation of samples carried out for nine different temperatures. This condition is carried out to see the effect of Roll Hot Press temperature on the size of the crystallite of PVDF films. To obtain the diffraction pattern of sample characterization is performed using X-Ray Diffraction. Furthermore, from the diffraction pattern is obtained, the calculation to determine the crystallite size of the sample by using the Scherrer equation. From the experimental results and the calculation of crystallite sizes obtained for the samples with temperature 130 °C up to 170 °C respectively increased from 7.2 nm up to 20.54 nm. These results show that increasing temperatures will also increase the size of the crystallite of the sample. This happens because with the increasing temperature causes the higher the degree of crystallization of PVDF film sample is formed, so that the crystallite size also increases. This condition indicates that the specific volume or size of the crystals depends on the magnitude of the temperature as it has been studied by Nakagawa.

Grafting of GMA and some comonomers onto chitosan for controlled release of diclofenac sodium.

Science.gov (United States)

Sharma, Rajeev Kr; Lalita; Singh, Anirudh P; Chauhan, Ghanshyam S

2014-03-01

In order to develop pH sensitive hydrogels for controlled drug release we have graft copolymerized glycidyl methacrylate (GMA) with comonomers acrylic acid, acrylamide and acrylonitrile, onto chitosan (Ch) by using potassium persulphate (KPS) as free radical initiator in aqueous solution. The optimum percent grafting for GMA was recorded for 1g chitosan at [KPS]=25.00 × 10(-3)mol/L, [GMA]=0.756 × 10(-3)mol/L, reaction temperature=60 °C and reaction time=1h in 20 mL H2O. Binary monomers were grafted for five different concentrations at optimum grafting conditions evaluated for GMA alone onto chitosan. The graft copolymers were characterized by FTIR, XRD, TGA and SEM. The swelling properties of chitosan and graft copolymers were investigated at different pH to define their end uses in sustained release of an anti-inflammatory drug, diclofenac sodium. Percent drug release w.r.t. drug loaded in polymeric sample was studied as function of time in buffer solutions of pH 2.0 and 7.4. In vitro release data was analyzed using Fick's Law. Chitosan grafted with binary monomers, GMA-co-AAm and GMA-co-AN showed very good results for sustained release of drug at 7.4 pH. Copyright © 2014 Elsevier B.V. All rights reserved.

Synthesis of Monodispersed Gold Nanoparticles with Exceptional Colloidal Stability with Grafted Polyethylene Glycol-g-polyvinyl Alcohol

Directory of Open Access Journals (Sweden)

Alaaldin M. Alkilany

2015-01-01

Full Text Available Herein, we report the synthesis of spherical gold nanoparticles with tunable core size (23–79 nm in the presence of polyethylene glycol-g-polyvinyl alcohol (PEG-g-PVA grafted copolymer as a reducing, capping, and stabilizing agent in a one-step protocol. The resulted PEG-g-PVA-capped gold nanoparticles are monodispersed with an exceptional colloidal stability against salt addition, repeated centrifugation, and extensive dialysis. The effect of various synthesis parameters and the kinetic/mechanism of the nanoparticle formation are discussed.

The facile synthesis of hierarchical NiCoO2 nanotubes comprised ultrathin nanosheets for supercapacitors

Science.gov (United States)

Xu, Xin; Zhou, Han; Ding, Shujiang; Li, Jun; Li, Beibei; Yu, Demei

2014-12-01

Hierarchical NiCoO2 nanosheets nanotubes are successfully prepared by a mild solution method based on the template of polymeric nanotubes (PNT) followed by a thermal annealing treatment. The microstructure and chemical composition of NiCoO2 nanosheets nanotubes are characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET) analyzer, X-ray diffraction (XRD) and Thermogravimetric analysis (TGA). When evaluated as an electrode material for supercapacitors, the results of electrochemical test show that the unique NiCoO2 nanosheets nanotubes exhibit relatively high specific capacitance of 1468, 1352, 1233, 1178, 1020 and 672 F g-1 at the discharge current densities of 2, 4, 8, 10, 20 and 40 A g-1, respectively. They also reveal an excellent cycling stability of 99.2% retention after 3000 cycles at 10 A g-1. The smart nanostructures of the NiCoO2 nanosheets nanotubes make a prominent contribution to the excellent electrochemical performance.

Numerical Simulation of Output Response of PVDF Sensor Attached on a Cantilever Beam Subjected to Impact Loading

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Cao Vu Dung

2016-04-01

Full Text Available Polyvinylidene Flouride (PVDF is a film-type polymer that has been used as sensors and actuators in various applications due to its mechanical toughness, flexibility, and low density. A PVDF sensor typically covers an area of the host structure over which mechanical stress/strain is averaged and converted to electrical energy. This study investigates the fundamental “stress-averaging” mechanism for dynamic strain sensing in the in-plane mode. A numerical simulation was conducted to simulate the “stress-averaging” mechanism of a PVDF sensor attached on a cantilever beam subjected to an impact loading, taking into account the contribution of piezoelectricity, the cantilever beam’s modal properties, and electronic signal conditioning. Impact tests and FEM analysis were also carried out to verify the numerical simulation results. The results of impact tests indicate the excellent capability of the attached PVDF sensor in capturing the fundamental natural frequencies of the cantilever beam. There is a good agreement between the PVDF sensor’s output voltage predicted by the numerical simulation and that obtained in the impact tests. Parametric studies were conducted to investigate the effects of sensor size and sensor position and it is shown that a larger sensor tends to generate higher output voltage than a smaller one at the same location. However, the effect of sensor location seems to be more significant for larger sensors due to the cancelling problem. Overall, PVDF sensors exhibit excellent sensing capability for in-plane dynamic strain induced by impact loading.

How Chain Intermixing Dictates the Polymorphism of PVDF in Poly(vinylidene fluoride/Polymethylmethacrylate Binary System during Recrystallization: A Comparative Study on Core–Shell Particles and Latex Blend

Directory of Open Access Journals (Sweden)

Yue Li

2017-09-01

Full Text Available In the past few decades, Poly(vinylidene fluoride/Polymethylmethacrylate (PVDF/PMMA binary blend has attracted substantial attention in the scientific community due to possible intriguing mechanical, optical and ferroelectric properties that are closely related to its multiple crystal structures/phases. However, the effect of PMMA phase on the polymorphism of PVDF, especially the relationship between miscibility and polymorphism, remains an open question and is not yet fully understood. In this work, three series of particle blends with varied levels of miscibility between PVDF and PMMA were prepared via seeded emulsion polymerization: PVDF–PMMA core–shell particle (PVDF@PMMA with high miscibility; PVDF/PMMA latex blend with modest miscibility; and PVDF@c–PMMA (crosslinked PMMA core–shell particle with negligible miscibility. The difference in miscibility, and the corresponding morphology and polymorphism were systematically studied to correlate the PMMA/PVDF miscibility with PVDF polymorphism. It is of interest to observe that the formation of polar β/γ phase during melt crystallization could be governed in two ways: dipole–dipole interaction and fast crystallization. For PVDF@PMMA and PVDF/PMMA systems, in which fast crystallization was unlikely triggered, higher content of β/γ phase, and intense suppression of crystallization temperature and capacity were observed in PVDF@PMMA, because high miscibility favored a higher intensity of overall dipole–dipole interaction and a longer interaction time. For PVDF@c–PMMA system, after a complete coverage of PVDF seeds by PMMA shells, nearly pure β/γ phase was obtained owing to the fast homogeneous nucleation. This is the first report that high miscibility between PVDF and PMMA could favor the formation of β/γ phase.

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.

Pancreas grafts

International Nuclear Information System (INIS)

Hahn, D.; Buell, U.; Land, W.; Unertl, K.

1981-01-01

Perfusion studies with sup(99m)Tc-DTPA, which has hitherto been used routinely to investigate renal grafts, have also proved useful for monitoring the perfusion of pancreas grafts. A total perfusion failure is equally reliably demonstrable as in renal grafts. Quantitatively smaller perfusion alterations can be demonstrated by monitoring the course. It seems possible to differentiate the salivary edema of a rejection reaction, well known from animal experiments, with the help of other paramters (e.g. creatinine). Further clinical studies are however necessary to confirm these results. (orig.) [de

Efficient removal of rhodamine 6G dye from aqueous solution using nickel sulphide incorporated polyacrylamide grafted gum karaya bionanocomposite hydrogel

CSIR Research Space (South Africa)

Kumar, N

2016-02-01

Full Text Available polymer of the Gk with the PAAm was synthesized using the graft co-polymerization technique. In the second step, the nickel sulphide nanoparticles were incorporated in situ within the hydrogel polymer matrix. The synthesized hydrogel nanocomposite...

Modeling and Optimization of NLDH/PVDF Ultrafiltration Nanocomposite Membrane Using Artificial Neural Network-Genetic Algorithm Hybrid.

Science.gov (United States)

Arefi-Oskoui, Samira; Khataee, Alireza; Vatanpour, Vahid

2017-07-10

In this research, MgAl-CO 3 2- nanolayered double hydroxide (NLDH) was synthesized through a facile coprecipitation method, followed by a hydrothermal treatment. The prepared NLDHs were used as a hydrophilic nanofiller for improving the performance of the PVDF-based ultrafiltration membranes. The main objective of this research was to obtain the optimized formula of NLDH/PVDF nanocomposite membrane presenting the best performance using computational techniques as a cost-effective method. For this aim, an artificial neural network (ANN) model was developed for modeling and expressing the relationship between the performance of the nanocomposite membrane (pure water flux, protein flux and flux recovery ratio) and the affecting parameters including the NLDH, PVP 29000 and polymer concentrations. The effects of the mentioned parameters and the interaction between the parameters were investigated using the contour plot predicted with the developed model. Scanning electron microscopy (SEM), atomic force microscopy (AFM), and water contact angle techniques were applied to characterize the nanocomposite membranes and to interpret the predictions of the ANN model. The developed ANN model was introduced to genetic algorithm (GA) as a bioinspired optimizer to determine the optimum values of input parameters leading to high pure water flux, protein flux, and flux recovery ratio. The optimum values for NLDH, PVP 29000 and the PVDF concentration were determined to be 0.54, 1, and 18 wt %, respectively. The performance of the nanocomposite membrane prepared using the optimum values proposed by GA was investigated experimentally, in which the results were in good agreement with the values predicted by ANN model with error lower than 6%. This good agreement confirmed that the nanocomposite membranes prformance could be successfully modeled and optimized by ANN-GA system.

Study of pyroelectric activity of PZT/PVDF-HFP composite

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Luiz Francisco Malmonge

2003-12-01

Full Text Available Flexible, free-standing piezo and pyroelectric composite with 0 to 3 connectivity was made up from Lead Zirconate Titanate (PZT powder and poly(vinylidene fluoride-hexafluoropropylene (PVDF-HFP copolymer. The pyroelectric and the piezoelectric longitudinal (d33 coefficients were measured. A 50/50 vol.% PZT/PVDF-HFP composite resulted in piezo and pyroelectric coefficients of d33 = 25.0 pC/N and p = 4.5 × 10-4 C/m²K at 70 °C, respectively. Analysis of the complex permittivity in a wide range of frequency was carried out indicating lower permittivity of the composite in comparison with a permittivity of the PZT ceramic. The low value of the permittivity gives a high pyroelectric figure of merit indicating that this material can be used to build a temperature sensor in spite of the lower pyroelectric coefficient compared with PZT.

Grafting heterogeneous catalyst with gamma radiation

International Nuclear Information System (INIS)

Garnett, J.L.; Long, M.A.; Levot, R.G.

1984-01-01

A process for the production of a heterogeneous catalyst comprises the steps of: irradiating an organic macromolecular substrate or a metal substrate with ionising or ultra violet radiation in the presence of a monomer selected from the group consisting of o-, m-, or p- styryl diphenyl phosphine and o-, m- or p- phenyl acrylyl diphenyl phosphine, to graft the monomer to the substrate; and reacting the graft copolymer with a homogeneous catalyst selected from the group consisting of catalytic metal salts and catalytic organometallic complexes such that the graft copolymer conjugate becomes a ligand of the catalyst

Effect of 60Co radiation-induced grafting of methyl methacrylate on mechanical properties of bamboo

International Nuclear Information System (INIS)

Zhang Hao; Zhou Liang; Liu Shengquan; Qian Liangcun; Fei Benhua; Jiang Zehui

2011-01-01

In order to investigate the effect of radiation grafting on mechanical properties of bamboo, the original and carbonized bamboo soaked with monomer MMA were radiation grafted by 60 Co γ rays with the doses of 60-220 kGy. The results showed that compared with original blanks, treated with MMA and irradiated with the dose of 180 kGy the specific gravity, bending strength modulus of elasticity of original bamboo increased by 6.7%, 4.4%, and 28%, meanwhile its oven-dried radial, tangential and volumetric shrinkage decreased by 38.9%, 47.4%, and 32.9%, respectively. What is more, treated with MMA and irradiated with the doses of 140 kGy the specific gravity and modulus of elasticity of carbonized bamboo increased by 6.8% and 20%, while its oven-dried radial, tangential, volumetric shrinkage decreased by 11%, 4.6% and 12%, respectively. The study reveals that mechanical properties of original and carbonized bamboo can be enhanced by radiation grafting copolymerization with suitable absorbed doses, which may be valuable for the further research of developing new bamboo plastic composites. (authors)

Fundamental characteristics study of anion-exchange PVDF-SiO(2) membranes.

Science.gov (United States)

Zuo, Xingtao; Shi, Wenxin; Yu, Shuili; He, Jiajie

2012-01-01

A new type of poly(vinylidene fluoride)(PVDF)-SiO(2) hybrid anion-exchange membrane was prepared by blending method. The anion-exchange groups were introduced by the reaction of epoxy groups with trimethylamine (TMA). Contact angle between water and the membrane surface was measured to characterize the hydrophilicity change of the membrane surface. The effects of nano-sized SiO(2) particles in the membrane-forming materials on the membrane mechanical properties and conductivity were also investigated. The experimental results indicated that PVDF-SiO(2) anion-exchange membranes exhibited better water content, ion-exchange capacity, conductivity and mechanic properties, and so may find potential applications in alkaline membrane fuel cells and water treatment processes.

Human exhaled air energy harvesting with specific reference to PVDF film

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Manisha Rajesh Mhetre

2017-02-01

Full Text Available Spirometer is a medical equipment used to measure lung capacity of a human being. It leads to diagnosis of several diseases. The researchers worked on harvesting energy from human exhalation while carrying out measurements using spirometer. A prototype has been developed using piezoelectric material i.e. PVDF (polyvinylidene fluoride film as sensor. This paper presents the methodology and experimentation carried out for exhaled air energy harvesting using PVDF film. Experimental results obtained are encouraging. Measurements are also carried out on various subjects having different height, weight, age and gender. Data analysis shows variation in the energy harvested with different physical parameters and gender. Experimentation shows that voltage generated due to exhaled air is promising for harvesting.

Radiation grafting on natural films

International Nuclear Information System (INIS)

Lacroix, M.; Khan, R.; Senna, M.; Sharmin, N.; Salmieri, S.; Safrany, A.

2014-01-01

Different methods of polymer grafting using gamma irradiation are reported in the present study for the preparation of newly functionalized biodegradable films, and some important properties related to their mechanical and barrier properties are described. Biodegradable films composed of zein and poly(vinyl alcohol) (PVA) were gamma-irradiated in presence of different ratios of acrylic acid (AAc) monomer for compatibilization purpose. Resulting grafted films (zein/PVA-g-AAc) had their puncture strength (PS=37–40 N mm −1 ) and puncture deformation (PD=6.5–9.8 mm) improved for 30% and 50% PVA in blend, with 5% AAc under 20 kGy. Methylcellulose (MC)-based films were irradiated in the presence of 2-hydroxyethyl methacrylate (HEMA) or silane, in order to determine the effect of monomer grafting on the mechanical properties of films. It was found that grafted films (MC-g-HEMA and MC-g-silane) using 35% monomer performed higher mechanical properties with PS values of 282–296 N mm −1 and PD of 5.0–5.5 mm under 10 kGy. Compatibilized polycaprolactone (PCL)/chitosan composites were developed via grafting silane in chitosan films. Resulting trilayer grafted composite film (PCL/chitosan-g-silane/PCL) presented superior tensile strength (TS=22 MPa) via possible improvement of interfacial adhesion (PCL/chitosan) when using 25% silane under 10 kGy. Finally, MC-based films containing crystalline nanocellulose (CNC) as a filling agent were prepared and irradiated in presence of trimethylolpropane trimethacrylate (TMPTMA) as a grafted plasticizer. Grafted films (MC-g-TMPTMA) presented superior mechanical properties with a TS of 47.9 MPa and a tensile modulus (TM) of 1792 MPa, possibly due to high yield formation of radicals to promote TMPTMA grafting during irradiation. The addition of CNC led to an additional improvement of the barrier properties, with a significant 25% reduction of water vapor permeability (WVP) of grafted films. - Highlights: • Irradiation of zein

Nanodiamond particles/PVDF nanocomposite flexible films: thermal, mechanical and physical properties

Science.gov (United States)

Jaleh, Babak; Sodagar, Shima; Momeni, Amir; Jabbari, Ameneh

2016-08-01

Recently, polymer nanocomposites reinforced with nanoparticles have attracted a lot of attention due to their unique physical and mechanical properties. In this work, poly (vinylidene fluoride)/nanodiamond particles nanocomposite films were prepared by solution casting method with various nanodiamond particles contents. The samples were investigated by Fourier transform infrared spectroscopy and x-ray diffraction technique. The results revealed an obvious α to β-phase transformation compared to pure PVDF. The most (or the maximum) phase transformation from α to β-phase (>90%) was found for nanocomposite film with 8% wt nanodiamond particles. Scanning electron micrographs showed considerable decrease in the size of spherulitic crystal structure of PVDF with adding nanoparticles. The photoluminescence property of nanocomposite films was investigated by photoluminescence spectroscopy and the optical band gap value was calculated from the UV-visible absorption spectra. The results showed that after the incorporation of nanoparticles into PVDF, the value of optical band gap decreased. Thermal stability of samples was studied by thermogravimetric analysis. Due to an increase in the electroactive phase (β) percentage by adding nanoparticles, the resistance of samples to thermal degradation improved. The mechanical properties of samples were investigated by tensile test and hardness measurements. The elastic modulus and hardness of samples were enhanced by adding nanodiamond particles and elongation to fracture decreased.

Fabrication of PVDF-based blend membrane with a thin hydrophilic deposition layer and a network structure supporting layer via the thermally induced phase separation followed by non-solvent induced phase separation process

Science.gov (United States)

Wu, Zhiguo; Cui, Zhenyu; Li, Tianyu; Qin, Shuhao; He, Benqiao; Han, Na; Li, Jianxin

2017-10-01

A simple strategy of thermally induced phase separation followed by non-solvent induced phase separation (TIPS-NIPS) is reported to fabricate poly (vinylidene fluoride) (PVDF)-based blend membrane. The dissolved poly (styrene-co-maleic anhydride) (SMA) in diluent prevents the crystallization of PVDF during the cooling process and deposites on the established PVDF matrix in the later extraction. Compared with traditional coating technique, this one-step TIPS-NIPS method can not only fabricate a supporting layer with an interconnected network structure even via solid-liquid phase separation of TIPS, but also form a uniform SMA skin layer approximately as thin as 200 nm via surface deposition of NIPS. Besides the better hydrophilicity, what's interesting is that the BSA rejection ratio increases from 48% to 94% with the increase of SMA, which indicates that the separation performance has improved. This strategy can be conveniently extended to the creation of firmly thin layer, surface functionalization and structure controllability of the membrane.

Surface Modification of Electrospun PVDF/PAN Nanofibrous Layers by Low Vacuum Plasma Treatment

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Fatma Yalcinkaya

2016-01-01

Full Text Available Nanofibres are very promising for water remediation due to their high porosity and small pore size. Mechanical properties of nanofibres restrict the application of pressure needed water treatments. Various PAN, PVDF, and PVDF/PAN nanofibre layers were produced, and mechanical properties were improved via a lamination process. Low vacuum plasma treatment was applied for the surface modification of nanofibres. Atmospheric air was used to improve hydrophilicity while sulphur hexafluoride gas was used to improve hydrophobicity of membranes. Hydrophilic membranes showed higher affinity to attach plasma particles compared to hydrophobic membranes.

Effects of static electricity and fabrication parameters on PVDF film ...

Indian Academy of Sciences (India)

2018-03-28

Mar 28, 2018 ... Degree of crystallinity and β-phase fraction are important factors in ... performance. In the present work, effects of intrinsic static electricity, substrate type, PVDF ... the best electroactive properties among all polymers [1] and.

Evaluation of the antifouling and photocatalytic properties of poly(vinylidene fluoride) plasma-grafted poly(acrylic acid) membrane with self-assembled TiO2

International Nuclear Information System (INIS)

You, Sheng-Jie; Semblante, Galilee Uy; Lu, Shao-Chung; Damodar, Rahul A.; Wei, Ta-Chin

2012-01-01

Highlights: ► Plasma and grafting parameters that maximized TiO 2 binding sites were found. ► PVDF hydrophilicity was vastly improved compared to other modification techniques. ► At least 1.5% TiO 2 and 30 min UV exposure were needed to attain full flux recovery. ► Photocatalytic membranes could remove up to 42% of 50 mg/l RB5 dye. - Abstract: Immobilization of TiO 2 is a promising approach that produces antifouling and photocatalytic membranes that could help advance wastewater treatment and re-use processes. In this study, poly(acrylic acid) (PAA) was plasma-grafted on commercial poly(vinylidene fluoride) (PVDF) to introduce functional groups on the membrane surface that can support the nanoparticles. It was found that plasma treatment at 100 W for 120 s followed by liquid grafting with 70% aqueous AA at 60 °C for 2 h maximized the number of TiO 2 binding sites. Membrane hydrophilicity was tremendously enhanced by the self-assembly of TiO 2 , following a direct proportionality to TiO 2 loading. The membrane with 0.5% TiO 2 loading maintained the highest pure water flux and the best protein antifouling property. UV irradiation triggered the photodegradation of strongly bound foulants, but at least 1.5% TiO 2 and 30 min cumulative irradiation were necessary to completely recover the membrane's original performance. The TiO 2 -modified membranes removed 30–42% of 50 mg/l aqueous Reactive Black 5 (RB5) dye. The fabricated membranes demonstrate huge potential for use in membrane reactors with high hydrophilicity, fouling mitigation, and photocatalytic capability.

Development of Novel Absorbents and Membranes by Radiation-Induced Grafting for Selective Purposes

Energy Technology Data Exchange (ETDEWEB)

Hegazy, E A; Abdel-Rehim, H; Hegazy, D; Ali, A A; Kamal, H; Sayed, A [National Center for Radiation Research and Technology, Atomic Energy Egypt, P.O.Box 29, Nasr City, Cairo (Egypt)

2012-09-15

The direct radiation grafting technique was used to graft glycidyl methacrylate (GMA) monomer containing epoxy ring, onto polypropylene fibres. The ring opening of the epoxy ring in GMA by different amino groups was studied to introduce various chelating agents. Some properties of grafted fibres were studied and the possibility of its practical use for water treatment from iron and manganese metals was investigated. The radiation initiated grafting of acrylic acid (AAc) or acrylamide (AAm) monomers onto poly(vinyl alcohol) (PVA), a 2-acrylamide-2-methyl propane sulfonic acid (AMPS) polymer was studied. Cationic/anionic membranes were also prepared by radiation-induced grafting of styrene/methacrylic acid (Sty/MAA) binary monomers onto LDPE films. To impart reactive cationic/anionic characters in the grafted membranes, sulfonation and alkaline treatments for styrene and carboxylic acid groups, respectively, were carried out. The possibility of their applications in the selective removal of some heavy metals was studied. The prepared grafted materials had a great ability to recover the metal ions such as: Ni{sup 2+}, Co{sup 2+}, Cu{sup 2+}, Cd{sup 2+}, Mg{sup 2+}, Zn{sup 2+}, Mn{sup 2+} and Cr{sup 3+} from their solutions. It was found that AMPS content in the grafted copolymers is the main parameter for the selectivity of the copolymer towards metal ions. The higher the AMPS content the higher the selectivity towards Co and Ni ions. In case of LDPE-g-P(STY/MAA), the sulfonation and alkaline treatments are the most effective methods to influence metal absorption and swelling behaviour of the prepared membranes. Graft composition, dose and pH have also a great influence on the membrane characteristics and applicability in wastewater treatments from heavy and toxic metals. Results revealed that the prepared grafted materials with different functionalized groups are promising as ion selective membranes and could be used for wastewater treatment. (author)

Effects of CO2 activation on electrochemical performance of microporous carbons derived from poly(vinylidene fluoride)

International Nuclear Information System (INIS)

Lee, Seul-Yi; Park, Soo-Jin

2013-01-01

In this work, we have prepared microporous carbons (MPCs) derived from poly(vinylidene fluoride) (PVDF), and the physical activation of MPCs using CO 2 gas is subsequently carried out with various activation temperatures to investigate the electrochemical performance. PVDF is successfully converted into MPCs with a high specific surface area and well-developed micropores. After CO 2 activation, the specific surface areas of MPCs (CA-MPCs) are enhanced by 12% compared with non-activated MPCs. With increasing activation temperature, the micropore size distributions of A-MPCs also become narrower and shift to larger pore size. It is also confirmed that the CO 2 activation had developed the micropores and introduced the oxygen-containing groups to MPCs′ surfaces. From the results, the specific capacitances of the electrodes in electric double layer capacitors (EDLCs) based on CA-MPCs are distinctly improved through CO 2 activation. The highest specific capacitance of the A-MPCs activated at 700 °C is about 125 F/g, an enhancement of 74% in comparison with NA-MPCs, at a discharge current of 2 A/g in a 6 M KOH electrolyte solution. We also found that micropore size of 0.67 nm has a specific impact on the capacitance behaviors, besides the specific surface area of the electrode samples. - Graphical abstract: The A-MPC samples with high specific surface area (ranging from 1030 to 1082 m 2 /g), corresponding to micropore sizes of 0.67 and 0.72 nm, and with the amount of oxygen-containing groups ranging from 3.2% to 4.4% have been evaluated as electrodes for EDLC applications. . Display Omitted - Highlights: • Microporous carbons (MPCs) were synthesized without activation process. • Next, we carried out the CO 2 activation of MPCs with activation temperatures. • It had developed the micropores and introduced the O-functional groups to MPCs. • The highest specific capacitance: 125 F/g, an increase of 74% compared to MPCs

UV-Induced [2+2] Grafting-To Reactions for Polymer Modification of Cellulose.

Science.gov (United States)

Conradi, Matthias; Ramakers, Gijs; Junkers, Thomas

2016-01-01

Benzaldehyde-functional cellulose paper sheets have been synthesized via tosylation of cellulose (Whatman No 5) followed by addition of p-hydroxy benzaldehyde. Via UV-induced Paterno-Büchi [2+2] cycloaddition reactions, these aldehyde functional surfaces are grafted with triallylcyanurate, trimethylolpropane allyl ether, and vinyl chloroacetate. In the following, allyl-functional polymers (poly(butyl acrylate), pBA, Mn = 6990 g mol(-1) , Đ = 1.12 and poly(N-isopropyl acrylamide), pNIPAAm, Mn = 9500 g mol(-1) , Đ = 1.16) synthesized via reversible addition fragmentation chain transfer polymerization are conjugated to the celloluse surface in a UV-induced grafting-to approach. With pBA, hydrophobic cellulose sheets are obtained (water contact angle 116°), while grafting of pNIPAAm allows for generation of "smart" surfaces, which are hydrophilic at room temperature, but that become hydrophobic when heated above the characteristic lower critical solution temperature (93° contact angle). The Paterno-Büchi reaction has been shown to be a versatile synthetic tool that also performs well in grafting-to approaches whereby its overall performance seems to be close to that of radical thiol-ene reactions. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes.

Science.gov (United States)

Hoop, Marcus; Chen, Xiang-Zhong; Ferrari, Aldo; Mushtaq, Fajer; Ghazaryan, Gagik; Tervoort, Theo; Poulikakos, Dimos; Nelson, Bradley; Pané, Salvador

2017-06-22

Electrical and/or electromechanical stimulation has been shown to play a significant role in regenerating various functionalities in soft tissues, such as tendons, muscles, and nerves. In this work, we investigate the piezoelectric polymer polyvinylidene fluoride (PVDF) as a potential substrate for wireless neuronal differentiation. Piezoelectric PVDF enables generation of electrical charges on its surface upon acoustic stimulation, inducing neuritogenesis of PC12 cells. We demonstrate that the effect of pure piezoelectric stimulation on neurite generation in PC12 cells is comparable to the ones induced by neuronal growth factor (NGF). In inhibitor experiments, our results indicate that dynamic stimulation of PVDF by ultrasonic (US) waves activates calcium channels, thus inducing the generation of neurites via a cyclic adenosine monophosphate (cAMP)-dependent pathway. This mechanism is independent from the well-studied NGF induced mitogen-activated protein kinases/extracellular signal-regulated kinases (MAPK/ERK) pathway. The use of US, in combination with piezoelectric polymers, is advantageous since focused power transmission can occur deep into biological tissues, which holds great promise for the development of non-invasive neuroregenerative devices.

Co-evolution of affinity and stability of grafted amyloid-motif domain antibodies.

Science.gov (United States)

Julian, Mark C; Lee, Christine C; Tiller, Kathryn E; Rabia, Lilia A; Day, Evan K; Schick, Arthur J; Tessier, Peter M

2015-10-01

An attractive approach for designing lead antibody candidates is to mimic natural protein interactions by grafting peptide recognition motifs into the complementarity-determining regions (CDRs). We are using this approach to generate single-domain (VH) antibodies specific for amyloid-forming proteins such as the Alzheimer's Aβ peptide. Here, we use random mutagenesis and yeast surface display to improve the binding affinity of a lead VH domain grafted with Aβ residues 33-42 in CDR3. Interestingly, co-selection for improved Aβ binding and VH display on the surface of yeast yields antibody domains with improved affinity and reduced stability. The highest affinity VH domains were strongly destabilized on the surface of yeast as well as unfolded when isolated as autonomous domains. In contrast, stable VH domains with improved affinity were reliably identified using yeast surface display by replacing the display antibody that recognizes a linear epitope tag at the terminus of both folded and unfolded VH domains with a conformational ligand (Protein A) that recognizes a discontinuous epitope on the framework of folded VH domains. Importantly, we find that selection for improved stability using Protein A without simultaneous co-selection for improved Aβ binding leads to strong enrichment for stabilizing mutations that reduce antigen binding. Our findings highlight the importance of simultaneously optimizing affinity and stability to improve the rapid isolation of well-folded and specific antibody fragments. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Utility of the indium 111-labeled human immunoglobulin G scan for the detection of focal vascular graft infection

International Nuclear Information System (INIS)

LaMuraglia, G.M.; Fischman, A.J.; Strauss, H.W.; Keech, F.; Wilkinson, R.; Callahan, R.J.; Khaw, B.A.; Rubin, R.H.

1989-01-01

The ability to diagnose and localize vascular graft infections has been a major challenge. Recent studies in animal models and humans with focal bacterial infection have shown that radiolabeled, polyclonal, human immunoglobulin G accumulates at the site of inflammation and can serve as the basis for an imaging technique. This study investigated this new technique for the diagnosis and localization of vascular graft infections. Twenty-five patients with suspected vascular infections involving grafts (22), atherosclerotic aneurysms (2), and subclavian vein thrombophlebitis (1) were studied. Gamma camera images of the suspected area were obtained between 5 and 48 hours after intravenous administration of 1.5 to 2.0 mCi (56 to 74 mBq) of indium 111-labeled, human, polyclonal immunoglobulin G. Scan results were interpreted without clinical information about the patient and were subsequently correlated with surgical findings, other imaging modalities, and/or clinical follow-up. In 10 of 10 patients found to have positive scan results, localized infections were confirmed at the involved sites. In 14 of 15 patients whose scan results were interpreted as negative, no vascular infections were identified at follow-up. The patient with false-negative results and recurrent bacteremia from an aortoduodenal fistula was found to have a negative scan outcome at a time when his disease was quiescent. These data suggest that nonspecific, human, indium 111-labeled immunoglobulin G scanning can be a useful noninvasive means of localizing vascular infections

Evaluation of early coronary graft patency after coronary artery bypass graft surgery using multislice computed tomography angiography

Directory of Open Access Journals (Sweden)

Raissi Kamal

2009-12-01

Full Text Available Abstract Background Coronary artery bypass graft (CABG surgery is the standard of care in the treatment of advanced coronary artery disease, and its long-term results are affected by the failure of bypass grafts. The aim of the present study was to evaluate the early patency rate in coronary bypass grafts. Methods A total of 107 consecutive patients who underwent CABG were included in this study. Early graft patency was evaluated via computed tomography (CT angiography in the first week after surgery. Results There were a total of 366 grafts, comprised of 250 venous grafts and 116 arterial grafts. Multi-slice CT detected acute graft occlusions in 32 (8.7% of all the grafts, including 26 (10% of the 250 venous grafts and 6 (5% of the 116 arterial grafts. The patency rates obtained were 97.3% for the left internal mammary (IMA grafts, 50% for the radial artery grafts, and 50% for the right IMA grafts. Additionally, 107 (96.4% grafts to the left anterior descending artery (LAD were classified as patent, whereas 1 (30% of the 3 grafts in the left circumflex (LCX region and 1 (50% of the 2 grafts in the right coronary artery (RCA territory were found to be occluded. In the venous category, 8 (13.7% of the 58 grafts to LAD were found to be occluded. In the LCX region, 9 (8.5% of the 106 grafts were classified as occluded, while the remaining 97 (91.5% grafts were patent. The venous grafts to RCA were occluded in 9 (10.4% of the 86 grafts. Amongst the multiple preoperative, intraoperative, and postoperative factors, pump time was significantly longer in the patients with occluded grafts than in those with patent grafts (P = 0.04. Conclusion The IMA grafts had the highest early patency rate amongst the coronary bypass grafts. However, the other arterial grafts were associated with a high rate of acute occlusions.

Optimized permeation and antifouling of PVDF hybrid ultrafiltration membranes: synergistic effect of dispersion and migration for fluorinated graphene oxide

Science.gov (United States)

Li, Mingming; Shi, Jie; Chen, Cheng; Li, Nan; Xu, Zhiwei; Li, Jing; Lv, Hanming; Qian, Xiaoming; Jiao, Xiaoning

2017-03-01

Nanoparticles may have suffered from low modification efficiency in hybrid membranes due to embedding and aggregating in polymer matrix. In order to analyze the modification mechanisms of nanoparticle migration and dispersion on the properties of hybrid membranes, we designed different F/ O ratios ( R F/ O ) of fluorinated graphene oxide (FGO, diameter = 1.5 17.5 μm) by carbon tetrafluoride (CF4) plasma treatment GO for 3, 5, 10, 15, and 20 min and successfully prepared novel PVDF hybrid membranes containing FGO via the phase inversion method. After a prolonged plasma treatment, the R F/ O of FGO was enhanced sharply, indicating an increasing compatibility of FGO with the matrix, especially FGO-20 (GO treated for 20 min). FGO contents in the top layer, sublayer, and the whole of membranes were probed by X-ray photoelectron spectroscopy, energy-dispersive spectrometer, and indirect computation, respectively. In the top layer of membranes, FGO contents declined from 13.14 wt% (PVDF/GO) to 4.00 wt% (PVDF/FGO-10) and 1.96 wt% (PVDF/FGO-20) due to the reduced migration ability of FGO. It is worth mentioning that PVDF/FGO-10 membranes exhibited an excellent water flux and flux recovery rate (up to 406.90 L m-2 h-1 and 88.9%), which were improved by 67.3% and 14.6% and 52.5% and 24.0% compared with those of PVDF/GO and PVDF/FGO-20 membranes, respectively, although the dispersion and migration ability of FGO-10 was maintained at a moderate level. It indicated that the migration and dispersion of FGO in membranes could result in dynamic equilibrium, which played a key role in making the best use of nanomaterials to optimize membrane performance.

Optimized permeation and antifouling of PVDF hybrid ultrafiltration membranes: synergistic effect of dispersion and migration for fluorinated graphene oxide

Energy Technology Data Exchange (ETDEWEB)

Li, Mingming; Shi, Jie; Chen, Cheng; Li, Nan; Xu, Zhiwei, E-mail: xuzhiwei@tjpu.edu.cn; Li, Jing; Lv, Hanming; Qian, Xiaoming, E-mail: qianxiaoming@tjpu.edu.cn; Jiao, Xiaoning [Tianjin Polytechnic University, State Key Laboratory of Separation Membranes and Membrane Processes, School of Textiles (China)

2017-03-15

Nanoparticles may have suffered from low modification efficiency in hybrid membranes due to embedding and aggregating in polymer matrix. In order to analyze the modification mechanisms of nanoparticle migration and dispersion on the properties of hybrid membranes, we designed different F/O ratios (R{sub F/O}) of fluorinated graphene oxide (FGO, diameter = 1.5 ~ 17.5 μm) by carbon tetrafluoride (CF{sub 4}) plasma treatment GO for 3, 5, 10, 15, and 20 min and successfully prepared novel PVDF hybrid membranes containing FGO via the phase inversion method. After a prolonged plasma treatment, the R{sub F/O} of FGO was enhanced sharply, indicating an increasing compatibility of FGO with the matrix, especially FGO-20 (GO treated for 20 min). FGO contents in the top layer, sublayer, and the whole of membranes were probed by X-ray photoelectron spectroscopy, energy-dispersive spectrometer, and indirect computation, respectively. In the top layer of membranes, FGO contents declined from 13.14 wt% (PVDF/GO) to 4.00 wt% (PVDF/FGO-10) and 1.96 wt% (PVDF/FGO-20) due to the reduced migration ability of FGO. It is worth mentioning that PVDF/FGO-10 membranes exhibited an excellent water flux and flux recovery rate (up to 406.90 L m{sup −2} h{sup −1} and 88.9%), which were improved by 67.3% and 14.6% and 52.5% and 24.0% compared with those of PVDF/GO and PVDF/FGO-20 membranes, respectively, although the dispersion and migration ability of FGO-10 was maintained at a moderate level. It indicated that the migration and dispersion of FGO in membranes could result in dynamic equilibrium, which played a key role in making the best use of nanomaterials to optimize membrane performance.

Electrochemical study on PVDF-HFP/silylated AI2O3-coated PE separators using the electron beam irradiation for lithium secondary battery

International Nuclear Information System (INIS)

Sohn, Joon Yong; Shin, Jun Hwa; Nho, Young Chang

2010-01-01

PVDF-HFP (binder)/silylated alumina (inorganic particle)-coated PE (polyethylene)separators were with various compositions of binder and inorganic particle were prepared by a dip-coating process with humidity control (R.H. 25% and 50%) using electron beam irradiation. The morphology of the coated PVDF-HFP/AI 2 O 3 layer with various compositions of PVDF-HFP and AI 2 O 3 , and humidity condition was found to be an important factor in determining ionic conductivity of the prepared separators. The PVDF-HFP/AI 2 O 3 (5/5)-coated PE separator prepared at R.H. 50% followed by electron beam irradiation at 200 kGy was applied for lithium-ion polymer battery and cell test results showed improved high-rate discharge performance and better cyclic stability compared to the cells with the bare PE and the PVDF-HFP-coated PE separators

Omega-3 PUFA concentration by a novel PVDF nano-composite membrane filled with nano-porous silica particles.

Science.gov (United States)

Ghasemian, Samaneh; Sahari, Mohammad Ali; Barzegar, Mohsen; Ahmadi Gavlighi, Hasan

2017-09-01

In this study, polyvinylidene fluoride (PVDF) and nano-porous silica particle were used to fabricate an asymmetric nano-composite membrane. Silica particles enhanced the thermal stability of PVDF/SiO 2 membranes; increasing the decomposition temperature from 371°C to 408°C. Cross sectional morphology showed that silica particles were dispersed in polymer matrix uniformly. However, particle agglomeration was found at higher loading of silica (i.e., 20 by weight%). The separation performance of nano-composite membranes was also evaluated using the omega-3 polyunsaturated fatty acids (PUFA) concentration at a temperature and pressure of 30°C and 4bar, respectively. Silica particle increased the omega-3PUFA concentration from 34.8 by weight% in neat PVDF to 53.9 by weight% in PVDF with 15 by weight% of silica. Moreover, PVDF/SiO 2 nano-composite membranes exhibited enhanced anti-fouling property compared to neat PVDF membrane. Fouling mechanism analysis revealed that complete pore blocking was the predominant mechanism occurring in oil filtration. The concentration of omega-3 polyunsaturated fatty acids (PUFA) is important in the oil industries. While the current methods demand high energy consumptions in concentrating the omega-3, membrane separation technology offers noticeable advantages in producing pure omega-3 PUFA. Moreover, concentrating omega-3 via membrane separation produces products in the triacylglycerol form which possess better oxidative stability. In this work, the detailed mechanisms of fouling which limits the performance of membrane separation were investigated. Incorporating silica particles to polymeric membrane resulted in the formation of mixed matrix membrane with improved anti-fouling behaviour compared to the neat polymeric membrane. Hence, the industrial potential of membrane processing to concentrate omega-3 fatty acids is enhanced. Copyright © 2017. Published by Elsevier Ltd.

Effects of CO{sub 2} activation on electrochemical performance of microporous carbons derived from poly(vinylidene fluoride)

Energy Technology Data Exchange (ETDEWEB)

Lee, Seul-Yi; Park, Soo-Jin, E-mail: sjpark@inha.ac.kr

2013-11-15

In this work, we have prepared microporous carbons (MPCs) derived from poly(vinylidene fluoride) (PVDF), and the physical activation of MPCs using CO{sub 2} gas is subsequently carried out with various activation temperatures to investigate the electrochemical performance. PVDF is successfully converted into MPCs with a high specific surface area and well-developed micropores. After CO{sub 2} activation, the specific surface areas of MPCs (CA-MPCs) are enhanced by 12% compared with non-activated MPCs. With increasing activation temperature, the micropore size distributions of A-MPCs also become narrower and shift to larger pore size. It is also confirmed that the CO{sub 2} activation had developed the micropores and introduced the oxygen-containing groups to MPCs′ surfaces. From the results, the specific capacitances of the electrodes in electric double layer capacitors (EDLCs) based on CA-MPCs are distinctly improved through CO{sub 2} activation. The highest specific capacitance of the A-MPCs activated at 700 °C is about 125 F/g, an enhancement of 74% in comparison with NA-MPCs, at a discharge current of 2 A/g in a 6 M KOH electrolyte solution. We also found that micropore size of 0.67 nm has a specific impact on the capacitance behaviors, besides the specific surface area of the electrode samples. - Graphical abstract: The A-MPC samples with high specific surface area (ranging from 1030 to 1082 m{sup 2}/g), corresponding to micropore sizes of 0.67 and 0.72 nm, and with the amount of oxygen-containing groups ranging from 3.2% to 4.4% have been evaluated as electrodes for EDLC applications. . Display Omitted - Highlights: • Microporous carbons (MPCs) were synthesized without activation process. • Next, we carried out the CO{sub 2} activation of MPCs with activation temperatures. • It had developed the micropores and introduced the O-functional groups to MPCs. • The highest specific capacitance: 125 F/g, an increase of 74% compared to MPCs.

Processing influence on the morphology of PVDF/PMMA blends examined by scanning electron microscopy

International Nuclear Information System (INIS)

Freire, Estevao; Forte, Maria M.C.; Monteiro, Elisabeth E.C.

2011-01-01

PVDF/PMMA blends were melt blended in proportions of 20, 40 e 60% PVDF by weight in two different mixers, a low shear and a high shear mixer. The compositions obtained were examined by scanning electron microscopy. The results were correlated with the two types of processing and showed that the type of mixer affects the morphology of the blend. The morphologies obtained corroborated the NMR analysis demonstrating the phase separation phenomena and the effect of the type of mixer used in this study. (author)

Structural, morphological and Raman studies on hybridized PVDF/BaTiO3 nanocomposites

Science.gov (United States)

Rajamanickam, N.; Jayakumar, K.; Ramachandran, K.

2017-05-01

Hybridized nanocomposites of polyvinylidene fluoride (PVDF) and nano - barium titanate (BaTiO3) were prepared using the solution casting method for different concentrations of nano-BaTiO3 and were characterized by X-ray diffraction and scanning electron microscopy. The flower like structure for morphology was observed in SEM. Raman analysis showed that the modified BaTiO3 particles, due to higher specific surfaces, induce, predominantly, the crystallization of the electrically active β-phase of PVDF, while the initial micron size particles induce the formation of the most common but non-polar α-crystal form.

Improvement of antithrombogenicity of a fluoro polymer by radiation-induced grafting of hydrophilic monomer

International Nuclear Information System (INIS)

Otsuhata, Kazushige; Razzak, M.T.; Tabata, Yoneho; Ohashi, Fumito; Takeuchi, Atsushi.

1985-01-01

Fluoro polymers have been used as biomaterials in medical field since they have good compatibility with both tissue and blood, and their biomaterial application are of variety. Blood compatibility of fluoro polymers, however, are not always enough for every applications. Especially, there is a large difficulty in the application for artificial vessel with small radius below than 4 mm. In the present study, grafting of a hydrophilic monomer onto a fluoro polymer has been carried out to improve blood compatibility of the fluoro polymer. The technique of grafting employed here was simultaneous irradiation method of gamma rays from a 60 Co source. The fluoro polymer and the hydrophilic monomer used in the experiment were alternative copolymer of ethylene and tetrafluoethylene(AFLON) and N,N-dimethylacry lamide(DMAA), respectively. After grafting, it was found by in vitro tests that antithrombogenicity of AFLON was improved by grafting of DMAA. It was, however, also found that degree of the improvement is affected by grafting conditions. When ethyl acetate was used as a solvent for the graft copolymerization, the improvement was affected by dose rate. Blood compatibility of DMAA-g-AFLON obtained at a higher dose rate of 1 x 10 5 rad/h was not improved, while it was improved in the sample of DMAA-g-AFLON obtained at a lower dose rate of 1 x 10 4 rad/h. On the other hand, when acetone was used as a solvent for the grafting, the degree of grafting gave a significant effect on the improvement. Blood compatibility of all samples with grafting percent more than 20 % was improved by grafting of DMAA. (author)

Treatment of lead contaminated water by a PVDF membrane that is modified by zirconium, phosphate and PVA.

Science.gov (United States)

Zhao, Dandan; Yu, Yang; Chen, J Paul

2016-09-15

Lead contamination is one of the most serious problems in drinking water facing humans. In this study, a novel zirconium phosphate modified polyvinyl alcohol (PVA)-PVDF membrane was developed for lead removal. The zirconium ions and PVA were firstly coated onto a PVDF membrane through crosslinking reactions with glutaraldehyde, which was then modified by phosphate. The adsorption kinetics study showed that most of ultimate uptake occurred in 5 h. The adsorption increased with an increase in pH; the optimal adsorption was achieved at pH 5.5. The experimental data were better described by Langmuir equation than Freundlich equation; the maximum adsorption capacity was 121.2 mg-Pb/g at pH 5.5, much higher than other reported adsorptive membranes. The membrane exhibited a higher selectivity for lead over zinc with a relative selectivity coefficient (Pb(2+)/Zn(2+)) of 9.92. The filtration study showed that the membrane with an area of 12.56 cm(2) could treat 13.9 L (equivalent to 73,000 bed volumes) of lead containing wastewater with an influent concentration of 224.5 μ g/L to meet the maximum contaminant level of 15 μ g/L. It was demonstrated that the membrane did well in the removal of lead in both simulated wastewater and lead-spiked reservoir water and had a good reusability in its applications. The XPS studies revealed that the lead uptake was mainly due to cation exchange between hydrogen ions and lead ions. Copyright © 2016 Elsevier Ltd. All rights reserved.

Synthesis of a pH- and Thermo- Responsive Binary Copolymer Poly(N-vinylimidazole-co-N-vinylcaprolactam Grafted onto Silicone Films

Directory of Open Access Journals (Sweden)

Ángela Obando-Mora

2015-10-01

Full Text Available This work focuses on the effects of gamma-ray irradiation conditions on the stimuli-responsiveness of silicone rubber (SR substrates grafted with N-vinylcaprolactam (NVCL and N-vinylimidazole (NVIM, modified by the simultaneously polymerization and grafting method, which is expected to result in valuable new applications in the near future. The modification of silicone rubber was carried out via γ-ray radiation in order to graft a binary copolymer, poly(N-vinylimidazole-co-N-vinylcaprolactam, by the pre-irradiation method, to obtain pH- and thermo-responsive materials. The grafting yield was found to be directly proportional to the dose and monomers concentration. The biomaterials were characterized by using Fourier-transform infrared attenuated total reflection (FTIR-ATR, differential scanning calorimetry (DSC, thermogravimetric analysis (TGA, and swelling; and their stimuli behavior was evaluated by lower critical solution temperature (LCST and pH critical studies.

Synthesis and characterization of poly[1-(N,N-bis-carboxymethyl)amino-3-allylglycerol-co-dimethylacrylamide] grafted to magnetic nano-particles for extraction and determination of letrozole in biological and pharmaceutical samples.

Science.gov (United States)

Ahmad Panahi, Homayon; Soltani, Elham Reza; Moniri, Elham; Tamadon, Atefeh

2013-12-15

In this paper, a new method is reported for the surface grafting of poly[1-(N,N-bis-carboxymethyl)amino-3-allylglycerol-co-dimethylacrylamide] onto magnetic nano-particles modified by 3-mercaptopropyltrimethoxysilane. The grafted nano-sorbent was characterized by Fourier transform infrared spectroscopy, elemental analysis, thermogravimetric analysis, and scanning electron microscopy. Agglomerated nano-particles with multi-pores were used for extraction and determination of trace letrozole in human biological fluids and pharmaceutical samples. The profile of the letrozole uptake by the magnetic nano-sorbent reflected good accessibility of the active sites in the grafted polymer. Scatchard analysis revealed that the sorption capacity of the functionalized nano-sorbent was 6.27 µmol g(-1) at an optimum pH of 4. The equilibrium adsorption data of letrozole by grafted magnetic nano-sorbent were analyzed by Langmuir, Freundlich, Temkin and Redlich-Peterson models. Conformation of the experimental data in the Langmuir isotherm model indicated the homogeneous binding site of functional polymer-grafted magnetic nano-sorbent surface. Nearly 89% of letrozole was released in simulated gastric fluid, pH 1.2, in 2h and 79% in simulated intestinal fluid, pH 7.4, in 30 h. These results show the utility of the letrozole loaded- polymer grafted magnetite nano-particles for enteric drug delivery. © 2013 Elsevier B.V. All rights reserved.

Gamma radiation grafting process for preparing separator membranes for electrochemical cells

International Nuclear Information System (INIS)

Agostino, V.F. D'; Lee, J.Y.

1982-01-01

An irradiation grafting process for preparing separator membranes for use in electrochemical cells, comprises contacting a polymeric base film with an aqueous solution of a hydrophilic monomer and a polymerization retardant; and irradiating said contacted film to form a graft membrane having low electrical resistivity and having monomer molecules uniformly grafted thereon. In the examples (meth) acrylic acid is grafted on to polyethylene, polypropylene and polytetrafluoroethylene in the presence of ferrous sulphate or cupric sulphate as polymerization retardants. (author)

A Four-Quadrant PVDF Transducer for Surface Acoustic Wave Detection

Directory of Open Access Journals (Sweden)

Zhi Chen

2012-08-01

Full Text Available In this paper, a polyvinylidene fluoride (PVDF piezoelectric transducer was developed to detect laser-induced surface acoustic waves in a SiO₂-thin film–Si-substrate structure. In order to solve the problems related to, firstly, the position of the probe, and secondly, the fact that signals at different points cannot be detected simultaneously during the detection process, a four-quadrant surface acoustic wave PVDF transducer was designed and constructed for the purpose of detecting surface acoustic waves excited by a pulse laser line source. The experimental results of the four-quadrant piezoelectric detection in comparison with the commercial nanoindentation technology were consistent, the relative error is 0.56%, and the system eliminates the piezoelectric surface wave detection direction deviation errors, improves the accuracy of the testing system by 1.30%, achieving the acquisition at the same time at different testing positions of the sample.

Improved PVDF membrane performance by doping extracellular polymeric substances of activated sludge.

Science.gov (United States)

Guan, Yan-Fang; Huang, Bao-Cheng; Qian, Chen; Wang, Long-Fei; Yu, Han-Qing

2017-04-15

Polyvinylidene fluoride (PVDF) membrane has been widely applied in water and wastewater treatment because of its high mechanical strength, thermal stability and chemical resistance. However, the hydrophobic nature of PVDF membrane makes it readily fouled, substantially reducing water flux and overall membrane rejection ability. In this work, an in-situ blending modifier, i.e., extracellular polymeric substances (EPS) from activated sludge, was used to enhance the anti-fouling ability of PVDF membrane. Results indicate that the pure water flux of the membrane and its anti-fouling performance were substantially improved by blending 8% EPS into the membrane. By introducing EPS, the membrane hydrophilicity was increased and the cross section morphology was changed when it interacted with polyvinl pyrrolidone, resulting in the formation of large cavities below the finger-like pores. In addition, the fraction of pores with a size of 100-500 nm increased, which was also beneficial to improving membrane performance. Surface thermodynamic calculations indicate the EPS-functionalized membrane had a higher cohesion free energy, implying its good pollutant rejection and anti-fouling ability. This work provides a simple, efficient and cost-effective method to improve membrane performance and also extends the applications of EPS. Copyright © 2017 Elsevier Ltd. All rights reserved.

Synthesis and characterization of PEPO grafted carboxymethyl guar and carboxymethyl tamarind as new thermo-associating polymers.

Science.gov (United States)

Gupta, Nivika R; Torris A T, Arun; Wadgaonkar, Prakash P; Rajamohanan, P R; Ducouret, Guylaine; Hourdet, Dominique; Creton, Costantino; Badiger, Manohar V

2015-03-06

New thermo associating polymers were designed and synthesized by grafting amino terminated poly(ethylene oxide-co-propylene oxide) (PEPO) onto carboxymethyl guar (CMG) and carboxymethyl tamarind (CMT). The grafting was performed by coupling reaction between NH2 groups of PEPO and COOH groups of CMG and CMT using water-soluble EDC/NHS as coupling agents. The grafting efficiency and the temperature of thermo-association, T(assoc) in the copolymer were studied by NMR spectroscopy. The graft copolymers, CMG-g-PEPO and CMT-g-PEPO exhibited interesting thermo-associating behavior which was evidenced by the detailed rheological and fluorescence measurements. The visco-elastic properties (storage modulus, G'; loss modulus, G") of the copolymer solutions were investigated using oscillatory shear experiments. The influence of salt and surfactant on the T(assoc) was also studied by rheology, where the phenomenon of "Salting out" and "Salting in" was observed for salt and surfactant, respectively, which can give an easy access to tunable properties of these copolymers. These thermo-associating polymers with biodegradable nature of CMG and CMT can have potential applications as smart injectables in controlled release technology and as thickeners in cosmetics and pharmaceutical formulations. Copyright © 2014 Elsevier Ltd. All rights reserved.

Studies on radiation-induced graft polymerization

International Nuclear Information System (INIS)

Omichi, Hideki

1978-09-01

Radiation-induced graft polymerization is used extensively to improve physical properties of polymers, but few processes are now commercialized. The reason for this is partly inadequate basic research on the reaction and partly the difficulty in developing the grafting process with large radiation source. Firstly, new techniques are proposed of studying kinetics of the graft polymerization in heterogeneous system. Based on the grafting yield, the molecular weight of graft chains, and the amount of radicals given by ESR and activation analysis, kinetic parameters are obtained and the reaction mechanism of grafting process is discussed. Secondly, the development of grafting process of poly (vinyl chloride)-butadiene is described. By study of the reaction, process design, construction and operation of the pilot plant, and economic analysis of the process, this process with 60 Co gamma ray sources is shown to be industrially promising. (author)

PDMS/PVDF hybrid electrospun membrane with superhydrophobic property and drop impact dynamics for dyeing wastewater treatment using membrane distillation

KAUST Repository

An, Alicia Kyoungjin; Guo, Jiaxin; Lee, Eui-Jong; Jeong, Sanghyun; Zhao, Yanhua; Wang, Zuankai; Leiknes, TorOve

2016-01-01

.4°) and roughness (Ra = 1,285mm). The zeta potential of E-PDMS membrane surface showed a higher negative value than that of a commercial PVDF (C-PVDF) membrane. These properties of E-PDMS membrane provided an antifouling in treating of differently-charged dyes

Hollow fiber membrane lumen modified by polyzwitterionic grafting

KAUST Repository

Le, Ngoc Lieu

2016-08-24

In this study, we demonstrate an effective way to modify the lumen of polyetherimide hollow fibers by grafting zwitterionic poly(sulfobetaine) to increase the membrane resistance to fouling. Surface-selective grafting of the protective hydrogel layers has been achieved in a facile two-step process. The first step is the adsorption of a macromolecular redox co-initiator on the lumen-side surface of the membrane, which in the second step, after flushing the lumen of the membrane with a solution comprising monomers and a complementary redox initiator, triggers the in situ cross-linking copolymerization at room temperature. The success of grafting reaction has been verified by the surface elemental analyses using X-ray photoelectron spectroscopy (XPS) and the surface charge evaluation using zeta potential measurements. The hydrophilicity of the grafted porous substrate is improved as indicated by the change of contact angle value from 44° to 30°, due to the hydration layer on the surface produced by the zwitterionic poly(sulfobetaine). Compared to the pristine polyetherimide (PEI) substrate, the poly(sulfobetaine) grafted substrates exhibit high fouling resistance against bovine serum albumin (BSA) adsorption, E. coli attachment and cell growth on the surface. Fouling minimization in the lumen is important for the use of hollow fibers in different processes. For instance, it is needed to preserve power density of pressure-retarded osmosis (PRO). In high-pressure PRO tests, a control membrane based on PEI with an external polyamide selective layer was seriously fouled by BSA, leading to a high water flux drop of 37%. In comparison, the analogous membrane, whose lumen was modified with poly(sulfobetaine), not only had a less water flux decline but also had better flux recovery, up to 87% after cleaning and hydraulic pressure impulsion. Clearly, grafting PRO hollow fiber membranes with zwitterionic polymeric hydrogels as a protective layer potentially sustains PRO

Development of highly porous flat sheet polyvinylidene fluoride (PVDF) membranes for membrane distillation

KAUST Repository

Alsaery, Salim A.

2017-05-01

With the increase of population every year, fresh water scarcity has rapidly increased and it is reaching a risky level, particularly in Africa and the Middle East. Desalination of seawater is an essential process for fresh water generation. One of the methods for desalination is membrane distillation (MD). MD process separates an aqueous liquid feed across a porous hydrophobic membrane to produce pure water via evaporation. Polyvinlidene fluoride (PVDF) membranes reinforced with a polyester fabric were fabricated as potential candidates for MD. Non-solvent induced phase separation coupled with steam treatment was used to prepare the PVDF membranes. A portion of the prepared membrane was coated with Teflon (AF2400) to increase its hydrophobicity. In the first study, the fabricated membranes were characterized using scanning electron microscopy and other techniques, and they were evaluated using direct contact MD (DCMD). The fabricated membranes showed a porous sponge-like structure with some macrovoids. The macrovoid formation and the spongy structure in the membrane cross-sections contributed significantly to a high permeate flux as they provide a large space for vapor water transport. The modified PVDF membranes with steaming and coating exhibited a permeate flux of around 40 L/h m2 (i.e. 27-30% increase to the control PVDF membrane) at temperatures of 60 °C (feed) and 20 °C (permeate). This increase in the permeate flux for the modified membranes was mainly attributed to its larger pore size on the bottom surface. In the second study, the control PVDF membrane was tested in two different module designs (i.e. semi-circular pipe and rectangular duct module designs). The semi-circular module design (turbulent regime) exhibited a higher permeate flux, 3-fold higher than that of the rectangular duct module design (laminar regime) at feed temperature of 60 °C. Furthermore, a heat energy balance was performed for each module design to determine the temperature

Supported Ionic Liquid Membranes and Ion-Jelly® Membranes with [BMIM][DCA]: Comparison of Its Performance for CO2 Separation

Directory of Open Access Journals (Sweden)

Ricardo Couto

2015-01-01

Full Text Available In this work, a supported ionic liquid membrane (SILM was prepared by impregnating a PVDF membrane with 1-butyl-3-methylimidazolium dicyanamide ([BMIM][DCA] ionic liquid. This membrane was tested for its permeability to pure gases (CO2, N2 and O2 and ideal selectivities were calculated. The SILM performance was also compared to that of Ion-Jelly® membranes, a new type of gelled membranes developed recently. It was found that the PVDF membrane presents permeabilities for pure gases similar or lower to those presented by the Ion-Jelly® membranes, but with increased ideal selectivities. This membrane presents also the highest ideal selectivity (73 for the separation of CO2 from N2 when compared with SILMs using the same PVDF support but with different ionic liquids.

BALLISTIC RESISTANT ARTICLES COMPRISING TAPES

NARCIS (Netherlands)

VAN DER EEM, JORIS; HARINGS, JULES; JANSE, GERARDUS; TJADEN, HENDRIK

2015-01-01

The invention pertains to a ballistic-resistant moulded article comprising a compressed stack of sheets comprising reinforcing tapes having a tensile strength of at least 1.0 GPa, a tensile modulus of at least 40 GPa, and a tensile energy-to-break of at least 15 J/g, the direction of the tapes

Direct-write PVDF nonwoven fiber fabric energy harvesters via the hollow cylindrical near-field electrospinning process

International Nuclear Information System (INIS)

Liu, Z H; Pan, C T; Ou, Z Y; Lin, L W; Huang, J C

2014-01-01

One-dimensional piezoelectric nanomaterials have attracted great attention in recent years for their possible applications in mechanical energy scavenging devices. However, it is difficult to control the structural diameter, length, and density of these fibers fabricated by micro/nano-technologies. This work presents a hollow cylindrical near-field electrospinning (HCNFES) process to address production and performance issues encountered previously in either far-field electrospinning (FFES) or near-field electrospinning (NFES) processes. Oriented polyvinylidene fluoride (PVDF) fibers in the form of nonwoven fabric have been directly written on a glass tube for aligned piezoelectricity. Under a high in situ electrical poling field and strong mechanical stretching (the tangential speed on the glass tube collector is about 1989.3 mm s −1 ), the HCNFES process is able to uniformly deposit large arrays of PVDF fibers with good concentrations of piezoelectric β-phase. The nonwoven fiber fabric (NFF) is transferred onto a polyethylene terephthalate (PET) substrate and fixed at both ends using copper foil electrodes as a flexible textile-fiber-based PVDF energy harvester. Repeated stretching and releasing of PVDF NFF with a strain of 0.05% at 7 Hz produces a maximum peak voltage and current at 76 mV and 39 nA, respectively. (paper)

Synthesis of Radiation Grafted Polymer Matrices for Separation and Industrial Applications

Energy Technology Data Exchange (ETDEWEB)

Bhardwaj, Y K; Virendra, K; Goel, N K; Sarma, K S.S.; Sabharwal, S [Radiation Technology Development Division, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085 (India)

2012-09-15

Grafting of acrylonitrile onto non-woven porous polypropylene fibre sheet using electron beam was carried out by post-irradiation grafting. Grafting extent of {approx}125% was achieved. The grafted nitrile groups were amidoximated and studied for uranium uptake from sea water and heavy metal ions (Co{sup 2+}, Ni{sup 2+}, Mn{sup 2+}, and Cd{sup 2+}) from aqueous solutions. Adsorption and elution of adsorbed ions in suitable eluents was studied. The grafting process was upgraded to pilot scale to obtain 1x1 m{sup 2} sheets. Mutual radiation grafting technique was used for grafting of vinylbenzyltrimethyl ammonium chloride, [2- (methacryloyloxy)ethyl] trimethylammonium chloride and [2-(acryloyloxyethyl)]trimethylammonium chloride onto cotton cellulose substrate. The grafted matrices showed significantly higher water uptake and good water retention properties. The antibacterial efficacy of the grafted products was found to be a function of extent of grafting and the type of bacteria (Escherichia coli, Pseudomonas flourescens, Staphylococcus aureus and Bacillus cereus). PVBT-g-cotton was studied for its protein adsorption behaviour in continuous column process using Bovine serum albumin (BSA) as a model protein. Mutual radiation grafting technique was used to graft acrylic acid on micrometer thick micro-porous polypropylene membrane. Contact angle measurement studies showed that initial grafting as well as radiation treatment of poly(propylene) in aqueous medium and in presence of Mohr's salt enhances its affinity towards the grafting solution. The enhancement in the polar component of surface energy of treated polypropylene membrane is the primary cause of grafting enhancement. The membranes grafted to an extent of {approx}20% were found to perform comparably with the battery separator presently being used by battery industry. Acrylic acid was grafted to Teflon scrap by mutual radiation grafting technique. The grafting extent decreased with increasing dose rate and

A robust and stretchable superhydrophobic PDMS/PVDF@KNFs membrane for oil/water separation and flame retardancy.

Science.gov (United States)

Li, Deke; Gou, Xuelian; Wu, Daheng; Guo, Zhiguang

2018-04-05

The wide application of superhydrophobic membranes has been limited due to their complicated preparation technology and weak durability. Inspired by the mechanical flexibility of nanofibrous biomaterials, nanofibrils have been successfully generated from Kevlar, which is one of the strongest synthetic fibers, by appropriate hydrothermal treatment. In this study, a robust superhydrophobic PDMS/PVDF@KNFs membrane is prepared via a simple one-step process and subsequent curing without combination with inorganic fillers. The as-prepared PDMS/PVDF@KNFs membrane not only shows efficient oil/water separation ability and oil absorption capacity but also has excellent superhydrophobicity stability after deformation. The resultant membrane shows stretchability, flexibility and flame retardance because of the reinforcing effect and the excellent flame retardancy of Kevlar. We believe that this simple fabrication of PDMS/PVDF@KNFs has promising applications in filtering membranes and wearable devices.

Poling effects on anisotropic temperature changes in NMR second moments of drawn PVDF films

International Nuclear Information System (INIS)

Ishii, Fumiaki; Sawatari, Takanori; Odajima, Akira

1982-01-01

For the drawn PVDF film, the NMR second moment vs temperature curves at 0 0 and 90 0 of the alignment angle (γ) cross over each other during the motional narrowing in the Tsub(g) region (-- -50 0 C). On poling, however, they decrease almost in parallel up to -20 0 C and show another narrowing above 30 0 C depending strongly on γ. These findings indicate that the molecular chain is oriented in the non-crystalline region and the poling more clearly separates low orientations from high orientations. The increase in the high orientation part should be attributed to polarization in the oriented non-crystalline region. (author)

Superhydrophobicity and regeneration of PVDF/SiO2 composite films

Science.gov (United States)

Liu, Tao; Li, Xianfeng; Wang, Daohui; Huang, Qinglin; Liu, Zhen; Li, Nana; Xiao, Changfa

2017-02-01

Superhydrophobicity of polymers is easily destroyed by careless touching due to the softness of microstructures. In this study, based on a well-constructed polyvinylidene fluoride (PVDF) surface, a novel superhydrophobic PVDF/SiO2 composite film was fabricated by adding hydrophobic SiO2 nanoparticle and solvent into a coagulation bath. The water contact angle of the composite film reached 162.3° and the sliding angle was as low as 1.5°. More importantly, the composite film could be regenerated only through immersing the composite film in the designed regeneration agent. The composition of the designed regeneration agent ensured that SiO2 nanoparticles were firmly adhered on the film surface even under the ultrasonic cleaning. Hence, the superhydrophobicity and self-cleaing property could be regenerated and maintained effectively, and moreover, these propeties could resist a proper pressure. In addition, after many rubbing-regenerating cycles, the regeneration method was still valid.

Effect of surface texture of grafted films on antithrombogenicity

International Nuclear Information System (INIS)

Otsuhata, K.; Razzak, M.T.; Castanares, R.L.; Tabata, Y.; Ohashi, F.; Takkeuchi, A.

1985-01-01

The relation between grafting conditions and antithrombogenicity has been examined from the purpose of clearing the necessity of controlling grafting conditions to enhance blood compatibility. The grafting systems employed here were N,N-dimethylacrylamide (DMAA) - poly(tetrafluoroethylene) (PTFE) and DMAA - poly(ethylene-co-tetrafluoroethylene) (AFLON) and grafting parameters were dose rate, monomer concentration and total dose (irradiation time). Grafting DMAA on to the substrates was carried out by using simultaneous irradiation method of gamma rays from a 60 Co source. After evaluation of blood compatibility of the grafted films by using in vitro tests, it has been clear that control of grafting conditions is important. Especially, in both grafting systems, dose rate control has found to be very important for blood compatibility. When higher dose rate of 1.0 x 10 5 to 3.0 x 10 5 rad/hr was used for grafting DMAA on to PTFE or AFLON, blood compatibility of the substrates was not enhanced, whereas it was improved when the grafting was carried out at lower dose rate of 0.97 x 10 4 rad/hr. The correlation between dose rate and antithrombogenicity has been interpreted in terms of surface-roughness of the grafted films. By scanning electron microscope (SEM) - observation, it has been observed that higher dose rate makes the surface rough, whereas lower dose rate makes it smooth. (author)

Graft polymerization of styrene onto starch by simultaneous cobalt-60 irradiation

International Nuclear Information System (INIS)

Fanta, G.F.; Burr, R.C.; Doane, W.M.; Russell, C.R.

1977-01-01

Starch-g-polystyrene copolymers have been prepared by the simultaneous 60 Co irradiation of starch--styrene mixtures, and copolymers have been characterized with respect to weight per cent polystyrene (% add-on) and also the molecular weight and molecular weight distribution of polystyrene grafts. In a typical polymerization, 4g each of starch and styrene were blended with 1 ml water and 1.5 ml of an organic solvent; the resulting semisolid paste was irradiated to a total dose of 1 Mrad. With ethylene glycol, acetonitrile, ethanol, methanol, acetone, and dimethylformamide as the organic solvent, values for % add-on ranged from 24% to 29%. The highest % add-on (43%) and the highest conversion of styrene to grafted polymer (76%) were obtained when the organic solvent was omitted, and water alone was used. When water was also omitted, polymerization of styrene was negligible; however, graft copolymer was formed in the absence of water when either ethylene glycol or ethanol was added. Attempts were unsuccessful to achieve a % add-on greater than 43% by doubling the amount of styrene in the polymerization recipe. Mixtures of equal weights of starch and styrene are relatively nonviscous, but these mixtures thicken when either water or ethylene glycol is blended in. Reasons for this thickening action and the possible influence of thickening on the graft polymerization reaction were explored

Surface Grafted Glycopolymer Brushes to Enhance Selective Adhesion of HepG2 Cells

DEFF Research Database (Denmark)

Chernyy, Sergey; Jensen, Bettina Elisabeth Brøgger; Shimizu, Kyoko

2013-01-01

on the polymerization kinetics of 2-lactobionamidoethyl methacrylate) (LAMA) monomer on thermally oxidized silicon wafer. Both monolayer and multilayered aminosilane precursor layers have been prepared followed by reaction with 2-bromoisobutyrylbromide to form the ATRP initiator layer. It is inferred from the kinetic...... studies that the rate of termination is low on a multilayered initiator layer compared to a disordered monolayer structure. However both initiator types results in similar graft densities. Furthermore, it is shown that thick comb-like poly(LAMA) brushes can be constructed by initiating a second ATRP...... process on a previously formed poly(LAMA) brushes. The morphology of human hepatocellular carcinoma cancer cells (HepG2) on the comb-like poly(LAMA) brush layer has been studied. The fluorescent images of the HepG2 cells on the glycopolymer brush surface display distinct protrusions that extend outside...

Evaluation of the antifouling and photocatalytic properties of poly(vinylidene fluoride) plasma-grafted poly(acrylic acid) membrane with self-assembled TiO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

You, Sheng-Jie, E-mail: sjyou@cycu.edu.tw [Department of Bioenvironmental Engineering, Chung Yuan Christian University, Chungli, Taiwan (China); R and D Center for Membrane Technology, Chung Yuan Christian University, Chungli, Taiwan (China); Semblante, Galilee Uy [Department of Bioenvironmental Engineering, Chung Yuan Christian University, Chungli, Taiwan (China); R and D Center for Membrane Technology, Chung Yuan Christian University, Chungli, Taiwan (China); Lu, Shao-Chung [Department of Civil Engineering, Chung Yuan Christian University, Chungli, Taiwan (China); Damodar, Rahul A. [Department of Bioenvironmental Engineering, Chung Yuan Christian University, Chungli, Taiwan (China); R and D Center for Membrane Technology, Chung Yuan Christian University, Chungli, Taiwan (China); Wei, Ta-Chin [R and D Center for Membrane Technology, Chung Yuan Christian University, Chungli, Taiwan (China); Department of Chemical Engineering, Chung Yuan Christian University, Chungli, Taiwan (China)

2012-10-30

Highlights: Black-Right-Pointing-Pointer Plasma and grafting parameters that maximized TiO{sub 2} binding sites were found. Black-Right-Pointing-Pointer PVDF hydrophilicity was vastly improved compared to other modification techniques. Black-Right-Pointing-Pointer At least 1.5% TiO{sub 2} and 30 min UV exposure were needed to attain full flux recovery. Black-Right-Pointing-Pointer Photocatalytic membranes could remove up to 42% of 50 mg/l RB5 dye. - Abstract: Immobilization of TiO{sub 2} is a promising approach that produces antifouling and photocatalytic membranes that could help advance wastewater treatment and re-use processes. In this study, poly(acrylic acid) (PAA) was plasma-grafted on commercial poly(vinylidene fluoride) (PVDF) to introduce functional groups on the membrane surface that can support the nanoparticles. It was found that plasma treatment at 100 W for 120 s followed by liquid grafting with 70% aqueous AA at 60 Degree-Sign C for 2 h maximized the number of TiO{sub 2} binding sites. Membrane hydrophilicity was tremendously enhanced by the self-assembly of TiO{sub 2}, following a direct proportionality to TiO{sub 2} loading. The membrane with 0.5% TiO{sub 2} loading maintained the highest pure water flux and the best protein antifouling property. UV irradiation triggered the photodegradation of strongly bound foulants, but at least 1.5% TiO{sub 2} and 30 min cumulative irradiation were necessary to completely recover the membrane's original performance. The TiO{sub 2}-modified membranes removed 30-42% of 50 mg/l aqueous Reactive Black 5 (RB5) dye. The fabricated membranes demonstrate huge potential for use in membrane reactors with high hydrophilicity, fouling mitigation, and photocatalytic capability.

Comparison of neat and photo-crosslinked polyvinylidene fluoride-co-hexafluoropropylene thin film dielectrics formed by spin-coating

International Nuclear Information System (INIS)

Iyore, O.D.; Roodenko, K.; Winkler, P.S.; Noriega, J.R.; Vasselli, J.J.; Chabal, Y.J.; Gnade, B.E.

2013-01-01

We report the characterization of photo-crosslinked polyvinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) thin film, metal–insulator–metal capacitors fabricated using standard semiconductor processing techniques. We characterize the capacitors using in-situ vibrational spectroscopy during thermally-assisted poling and correlate the Fourier transform infrared spectroscopy (FTIR) results with X-ray diffraction (XRD) results. FTIR analysis of the neat PVDF-HFP showed α → β transformations during poling at room temperature and at 55 °C. α → β transformations were observed for the crosslinked polymer only during poling at 55 °C. XRD data revealed that photo-crosslinking caused the polymer to partially crystallize into the β-phase. The similar behavior of the neat and crosslinked samples at 55 °C suggests that a higher activation energy was needed for α → β transformations in crosslinked PVDF-HFP during poling. Electrical measurements showed that photo-crosslinking had no significant effect on the dielectric constant and dielectric loss of PVDF-HFP. However, the dielectric strength and maximum energy density of the crosslinked polymer were severely reduced. - Highlights: • Polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP) dielectrics were studied. • Phase transformations were observed only at 55 °C for the crosslinked PVDF-HFP. • Crosslinking had no strong effect on the dielectric constant of PVDF-HFP. • Breakdown strengths were 620 MVm −1 and 362 MVm −1 for neat and crosslinked films

Effects of magnetic field treatment on dielectric properties of CCTO@Ni/PVDF composite with low concentration of ceramic fillers

Energy Technology Data Exchange (ETDEWEB)

Chi, Q. G., E-mail: qgchi@hotmail.com, E-mail: empty-cy@l63.com [Key Laboratory of Engineering Dielectrics and Its Application, Ministry of Education, Harbin University of Science and Technology, Harbin 150080 (China); State Key Laboratory of Electrical Insulation and Power Equipment, Xi’an Jiaotong University, Xi’an 710049 (China); Gao, L. [Key Laboratory of Engineering Dielectrics and Its Application, Ministry of Education, Harbin University of Science and Technology, Harbin 150080 (China); College of Electrical Engineering, Suihua University, Suihua 152061 (China); Wang, X.; Chen, Y., E-mail: qgchi@hotmail.com, E-mail: empty-cy@l63.com; Dong, J. F.; Cui, Y.; Lei, Q. Q. [Key Laboratory of Engineering Dielectrics and Its Application, Ministry of Education, Harbin University of Science and Technology, Harbin 150080 (China)

2015-11-15

Using melt mixing, we produced a ceramic/polymer composite with a matrix of polyvinylidene fluoride (PVDF) and a filler of 5 vol.% Ni-deposited CaCu{sub 3}Ti{sub 4}O{sub 12} core-shell ceramic particles (CCTO@Ni), and studied its prominent dielectric characteristics for the first. Its phase composition and morphology were analyzed by X-ray diffraction and scanning electron microscopy, respectively. After treating the composite films with various durations of a magnetic field treatment, we compared their dielectric properties. We found that the CCTO@Ni ceramic had a typical urchin-like core-shell structure, and that different durations of the magnetic field treatment produced different distributions of ceramic particles in the PVDF matrix. The dielectric permittivity of the untreated CCTO@Ni/PVDF composite was 20% higher than that of neat PVDF, and it had a low loss tangent. However, only the composite treated for 30 min in the magnetic field had an ultra-high dielectric permittivity of 1.41 × 10{sup 4} at 10 Hz, three orders of magnitude higher than the untreated composite, which declined dramatically with increasing frequency, accompanied by an insulating-conducting phase transition and an increase in loss tangent. Our results demonstrate that changes in the dielectric properties of PVDF composites with magnetic field treatment are closely related to the percolation effect and interfacial polarization.

The effect of solid content on silylated-γ-AI2O3/PVDF-HFP-coated PE separators for lithium secondary battery

International Nuclear Information System (INIS)

Im, Jong Su; Sohn, Joon Yong; Shin, Jun Hwa; Nho, Young Chang; Kim, Jeong Soo

2009-01-01

Several PVDF-HFP/silylated γ-AI 2 O 3 -coated PE (polyethylene) separators with various solidities (various compositions of PVDF-HFP/silylated γ-AI 2 O 3 ) were prepared by a dip-coating of PE separators in PVDF-HFP/silylated γ-AI 2 O 3 /acetone mixtures. FT-IR spectroscopy was used to confirm the chemical reactions between silane coupling agent and γ-AI 2 O 3 . The SEM images of the coated separators showed that various morphologies could be produced by changing the composition of total contents of binder and solid contents. The effects of composition in inorganic material (silane coupling agent-treated γ-AI 2 O 3 ) and binder (PVDF-HFP) on the physio-chemical properties of the prepared separators such as liquid electrolyte uptake, and ion conductivity were investigated and reported in this paper

Modelling coupled to behaviour and damage; rupture criteria in the field of the PVDF transition; Modelisation couplee comportement endommagement et criteres de rupture dans le domaine de la transition du PVDF

Energy Technology Data Exchange (ETDEWEB)

Lafarge, M.

2004-12-15

Pipeline structures are used for the transport of crude oil in offshore fields. Flexible pipelines are made of an inner metallic layer, which accommodates flexural and tensile strains and of a PVDF layer, which guarantees watertightness. The aim of the study is to determine which conditions can lead to a risk of brittle fracture of the polymer material. The PVDF of interest was extruded without plasticizer and therefore it differs considerably from the standard industrial grade. The lack of plasticizer leads to a difficult extrusion, which creates significant porosity (10%). Several specimens with various geometries were tested in order to analyse the detrimental effect of a defect regarding damage evolution and fracture mechanisms. During the deformation process, the material is characterized by whitening due to void growth and material elongation. Ductile fracture of PVDF is promoted by high temperatures, low strain rates, low stress triaxiality ratios and flexural loading, whereas brittle fracture is favoured by low temperatures (T{<=}Tg = -42 C), high strain rates, high stress triaxiality ratios and tensile loading. The Gurson-Tvergaard-Needleman model, usually used for metallic materials, was employed to model behaviour and damage of PVDF material at various temperatures. Damage is essentially due to void growth and is described by using q1 and q2 parameters. The constitutive model has been successfully applied to account for all aspects of the mechanical behaviour of the material. Crazing is the failure mode and final fracture is assumed to occur when either, the maximum principal plastic strain at low stress triaxiality or the porosity at high stress triaxiality reaches respectively a critical value. Furthermore, the ductile to brittle transition criterion is found to be the maximum principal stress. This latter allows to explain both fracture mechanisms modes in flexural and tensile loading. (author)

Understanding the Effects of Defect Modification on the Structure and Properties of Fluorinated Polymers and Implications for Capacitive Energy Storage Technologies

Science.gov (United States)

Gadinski, Matthew R.

that only the size of the third bulky monomer (CTFE in this case) determines whether a single hysteresis (SHL) or double hysteresis loop (DHL) will develop. This chapter shows that for a single composition of the terpolymer normal ferroelectric, SHL, and DHL behavior can be tuned through processing of the film. This was rationalized as films give long times to crystallize developed large ferroelectric domains within a paraelectric matrix resulting in the DHL behavior due to reversible switching of these domains. While if these films were stretched below the Tc SHL behavior was observed as this had the effect of dispersing these domains within the crystal. Chapter 5 changes focus to high temperature performance of polymer capacitors. The primary strategy to enable high temperature polymer capacitors has been the utilization of high Tg polymers because of their thermal stability. While these polymers have demonstrated stable dielectric properties at low field and high breakdown strengths at elevated temperatures, the high field loss limits their use at even mildly elevated temperature well below T g. Additionally, these polymers are expensive, brittle, and difficult to process, essentially defeating some of the primary reasons for utilizing a polymer in the first place. This chapter examines a commercially available, extrudable, high temperature fluoropolymer, known as polychlorotrifluoroethylene (PCTFE). The same defect monomer discussed with PVDF above. While this polymer showed comparable performance to BOPP at room temperature, it showed equally susceptible to high field loss at elevated temperature. However, the chlorine of the monomers allow for crosslinking of this polymer by commercially used peroxide/co-agent chemistry. Crosslinking lead to a substantial improvement of the crosslinked film over the pristine polymer, and superior energy density to the commercial high Tg polymers up to 150 °C. The reason for the improvement was found to be the formation of

Electroactive and High Dielectric Folic Acid/PVDF Composite Film Rooted Simplistic Organic Photovoltaic Self-Charging Energy Storage Cell with Superior Energy Density and Storage Capability.

Science.gov (United States)

Roy, Swagata; Thakur, Pradip; Hoque, Nur Amin; Bagchi, Biswajoy; Sepay, Nayim; Khatun, Farha; Kool, Arpan; Das, Sukhen

2017-07-19

Herein we report a simplistic prototype approach to develop an organic photovoltaic self-charging energy storage cell (OPSESC) rooted with biopolymer folic acid (FA) modified high dielectric and electroactive β crystal enriched poly(vinylidene fluoride) (PVDF) composite (PFA) thin film. Comprehensive and exhaustive characterizations of the synthesized PFA composite films validate the proper formation of β-polymorphs in PVDF. Significant improvements of both β-phase crystallization (F(β) ≈ 71.4%) and dielectric constant (ε ≈ 218 at 20 Hz for PFA of 7.5 mass %) are the twosome realizations of our current study. Enhancement of β-phase nucleation in the composites can be thought as a contribution of the strong interaction of the FA particles with the PVDF chains. Maxwell-Wagner-Sillars (MWS) interfacial polarization approves the establishment of thermally stable high dielectric values measured over a wide temperature spectrum. The optimized high dielectric and electroactive films are further employed as an active energy storage material in designing our device named as OPSESC. Self-charging under visible light irradiation without an external biasing electrical field and simultaneous remarkable self-storage of photogenerated electrical energy are the two foremost aptitudes and the spotlight of our present investigation. Our as fabricated device delivers an impressively high energy density of 7.84 mWh/g and an excellent specific capacitance of 61 F/g which is superior relative to the other photon induced two electrode organic self-charging energy storage devices reported so far. Our device also proves the realistic utility with good recycling capability by facilitating commercially available light emitting diode.

Fabrication and actuation of electro-active polymer actuator based on PSMI-incorporated PVDF

Science.gov (United States)

Lu, Jun; Kim, Sang-Gyun; Lee, Sunwoo; Oh, Il-Kwon

2008-08-01

In this study, an ionic networking membrane (INM) of poly(styrene-alt-maleimide) (PSMI)-incorporated poly(vinylidene fluoride) (PVDF) was applied to fabricate electro-active polymer. Based on the same original membrane of PSMI-incorporated PVDF, various samples of INM actuator were prepared for different reduction times with the electroless-plating technique. The as-prepared INM actuators were tested in terms of surface resistance, platinum morphology, resonance frequency, tip displacement, current and blocked force, and their performances were compared to those of the widely used traditional Nafion actuator. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed that much smaller and more uniform platinum particles were formed on the surfaces of the INM actuators as well as within their polymer matrix. Although excellent harmonic responses were observed for the newly developed INM actuators, they were found to be sensitive to the applied reduction times during the fabrication. The mechanical displacement of the INM actuator fabricated after the optimum reduction times was much larger than that of its Nafion counterpart of comparable thickness under the stimulus of constant and alternating current voltage. The PSMI-incorporated PVDF actuator can become a promising smart material to be used in the fields of biomimetic robots, biomedical devices, sensors and actuator, haptic interfaces, energy harvesting and so on.

Fabrication and actuation of electro-active polymer actuator based on PSMI-incorporated PVDF

International Nuclear Information System (INIS)

Lu, Jun; Oh, Il-Kwon; Kim, Sang-Gyun; Lee, Sunwoo

2008-01-01

In this study, an ionic networking membrane (INM) of poly(styrene-alt-maleimide) (PSMI)-incorporated poly(vinylidene fluoride) (PVDF) was applied to fabricate electro-active polymer. Based on the same original membrane of PSMI-incorporated PVDF, various samples of INM actuator were prepared for different reduction times with the electroless-plating technique. The as-prepared INM actuators were tested in terms of surface resistance, platinum morphology, resonance frequency, tip displacement, current and blocked force, and their performances were compared to those of the widely used traditional Nafion actuator. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed that much smaller and more uniform platinum particles were formed on the surfaces of the INM actuators as well as within their polymer matrix. Although excellent harmonic responses were observed for the newly developed INM actuators, they were found to be sensitive to the applied reduction times during the fabrication. The mechanical displacement of the INM actuator fabricated after the optimum reduction times was much larger than that of its Nafion counterpart of comparable thickness under the stimulus of constant and alternating current voltage. The PSMI-incorporated PVDF actuator can become a promising smart material to be used in the fields of biomimetic robots, biomedical devices, sensors and actuator, haptic interfaces, energy harvesting and so on

Obtention of graft copolymers by ionizing radiation, characterization and study of hemo-compatible properties; Obtencao de copolimeros de enxerto via radiacao ionizante, caracterizacao e estudo de suas propriedades hemocompativeis

Energy Technology Data Exchange (ETDEWEB)

Queiroz, A A.A. de

1994-12-31

The present work had as objectives the obtention and characterization of grafting copolymers by radiation induced polymerization and the study of its hemo compatible properties. The relationship between grafting conditions and anti-trombogenicity was examined for the purpose of clearing the necessity of controlling grafting conditions to enhance the copolymers blood compatibility. Two methods were chosen to accomplish the irradiation: mutual and pre-irradiation (peroxidation) of the films in {sup 6O} Co source and electron beam accelerator. Primarily grafting parameters were studied in the systems of the monomers N, N-dimethyl acrylamide (DMAA) and acrylic acid (AA) with the polymeric films: poly (tetrafluoroethylene) (PTFE), poly (ethylene-co-tetrafluoroethylene) (PETFE), low density polyethylene (LDPE) and poly (vinyl chloride) (PVC). The simultaneous irradiation was effective in the polymerization of all the substrates above mentioned, although the peroxidation method has given better results for PETFE-DMAA, LDPE-g-DMAA, LDPE-g-AA and PVC-g-AA. In the system AA/LDPE and AA/PVC the homo polymerization was controlled by the addition of the comonomer N, N-dimethyl acrylic acid (DMA). As for the grafting parameters, low dose rate and low irradiation dose, showed to be very effective for the graftability of DMAA and AA on the substrates. (author). 129 refs, 51 figs, 7 tabs.

Comparative Performance of PLZT and PVDF Pyroelectric Sensors Used to the Thermal Characterization of Liquid Samples

Directory of Open Access Journals (Sweden)

Gemima Lara Hernandez

2013-01-01

Full Text Available Among the photothermal methods, the photopyroelectric (PPE technique is a suitable method to determine thermal properties of different kinds of samples ranging from solids to liquids and gases. Polyvinylidene difluoride (PVDF is one of the most frequently used pyroelectric sensors in PPE technique but has the disadvantage that it can be easily deformed by the sample weight. This deformation could add a piezoelectric effect to the thermal parameters assessment; also PVDF has a narrow temperature operation range when compared with ceramic pyroelectric sensors. In order to minimize possible piezoelectric effects due to sensor deformation, a ceramic of lanthanum modified lead zirconate (PLZT was used as pyroelectric sensor in the PPE technique. Then, thermal diffusivity of some liquid samples was measured, by using the PPE configuration that denominated the thermal wave resonator cavity (TWRC, with a PLZT ceramic as pyroelectric detector. The performance obtained with the proposed ceramic in the TWRC configuration was compared with that obtained with PVDF by using the same configuration.

Spectral response analysis of PVDF capacitive sensors

Science.gov (United States)

Reyes-Ramírez, B.; García-Segundo, C.; García-Valenzuela, A.

2013-06-01

We investigate the spectral response to ultrasound waves in water of low-noise capacitive sensors based on PVDF polymer piezoelectric films. First, we analyze theoretically the mechanical-to-electrical transduction as a function of the frequency of ultrasonic signals and derive an analytic expression of the sensor's transfer function. Then we present experimental results of the frequency response of a home-made PDVF in water to test signals from 1 to 20 MHz induced by a commercial hydrophone powered by a signal generator and compare with our theoretical model.

Current status of grafts and implants in rhinoplasty: Part II. Homologous grafts and allogenic implants.

Science.gov (United States)

Sajjadian, Ali; Naghshineh, Nima; Rubinstein, Roee

2010-03-01

After reading this article, the participant should be able to: 1. Understand the challenges in restoring volume and structural integrity in rhinoplasty. 2. Identify the appropriate uses of various homologous grafts and allogenic implants in reconstruction, including: (a) freeze-dried acellular allogenic cadaveric dermis grafts, (b) irradiated cartilage grafts, (c) hydroxyapatite mineral matrix, (d) silicone implants, (e) high-density polyethylene implants, (f) polytetrafluoroethylene implants, and (g) injectable filler materials. 3. Identify the advantages and disadvantages of each of these biomaterials. 4. Understand the specific techniques that may aid in the use these grafts or implants. This review specifically addresses the use of homologous grafts and allogenic implants in rhinoplasty. It is important to stress that autologous materials remain the preferred graft material for use in rhinoplasty, owing to their high biocompatibility and low risk of infection and extrusion. However, concerns of donor-site morbidity, graft availability, and graft resorption have motivated the development and use of homologous and allogenic implants.

Radiolytic preparation of PFA-g-PVBSA membranes as a polymer electrolyte membrane

Energy Technology Data Exchange (ETDEWEB)

Fei Geng [Department of Chemistry and Materials Engineering, Changshu Institute of Technology, Nansanhuan Road 99, Changshu, Jiangsu 215-500 (China); Hwang, Mi-Lim; Sohn, Joon-Yong; Nho, Young Chang [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 1266 Sinjeong-dong, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of); Shin, Junhwa, E-mail: shinj@kaeri.re.kr [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 1266 Sinjeong-dong, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of)

2012-03-01

In this study, a polymer electrolyte membrane, PFA-g-PVBSA was prepared through the radiation-induced graft copolymerization of vinylbenzyl chloride (VBC) monomer onto a poly(tetrafluoroethylene-co-perfluoropropylvinyl ether) (PFA) film and subsequent sulfonation processes. The IEC values and water uptakes of the prepared membranes increased when increasing the contents of the poly(vinylbenzyl sulfonic acid) (PVBSA) graft polymers in the membranes. Compared with Nafion 212, the degree of grafting (DOG) of membranes of 50% and 70% showed higher proton conductivity with significantly lower methanol permeability. The combination of these properties suggests that the prepared membranes are promising for future application in direct methanol fuel cells.

Radiation induced graft copolymerization of acrylamide onto poly (3-hydroxybutyrate)

International Nuclear Information System (INIS)

Gonzalez Torres, Maykel; Rapado Paneque, Manuel; Paredes Zaldivar, Mayte; Altanes Valentin, Sonia; Barrera Gonzalez, Gisela

2008-01-01

The graft copolymer poly (3-hydroxybutyrate)-g- polyacrylamide [P (HB-g-AAm)] was synthesized by radiation induced graft copolymerization of acrylamide onto poly (3-hydroxybutyrate). The study was conducted by the simultaneous irradiation method. The structure of [P (HB-g-AAm)] was identified by Fourier Transform Infrared (FTIR) spectroscopy. Thermal behavior of the graft copolymer was also studied by Thermal Gravimetric Analysis (TGA) and Differential Scanning Calorimetry (DSC). From the results it was found that FTIR studies showed new signals (stretching -N-H) as strong evidence of grafting. The grafting degree was found to be 10 % and the thermodynamic parameter obtained from the DSC thermogram of plain PHB and the graft copolymer varied showing decrease in the material crystallinity and increase in the glass transition temperature. These results demonstrate that the radiation induced graft copolymerization reaction of acrylamide onto PHB was successively achieved. (Author)

Polyethyleneglycol grafting of γ-alumina membranes for solvent resistant nanofiltration

NARCIS (Netherlands)

Tanardi, Cheryl; Catana, Romina; Barboiu, Mihai; Ayral, André; Vankelecom, Ivo F.J.; Nijmeijer, Arian; Winnubst, Aloysius J.A.

2016-01-01

A method is presented for grafting mesoporous g-alumina (pore size 5 nm), supported on an a-alumina ceramic membrane, with polyethylene glycols (PEG). The grafting performance of g-Al2O3 powders with various PEG grafting agents, having different molecular weights, alkoxy groups, and ureido

Physical properties of agave cellulose graft polymethyl methacrylate

Energy Technology Data Exchange (ETDEWEB)

Rosli, Noor Afizah; Ahmad, Ishak; Abdullah, Ibrahim; Anuar, Farah Hannan [Polymer Research Centre (PORCE), School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi Selangor (Malaysia)

2013-11-27

The grafting polymerization of methyl methacrylate and Agave cellulose was prepared and their structural analysis and morphology were investigated. The grafting reaction was carried out in an aqueous medium using ceric ammonium nitrate as an initiator. The structural analysis of the graft copolymers was carried out by Fourier transform infrared and X-ray diffraction. The graft copolymers were also characterized by field emission scanning electron microscopy (FESEM). An additional peak at 1732 cm{sup −1} which was attributed to the C=O of ester stretching vibration of poly(methyl methacrylate), appeared in the spectrum of grafted Agave cellulose. A slight decrease of crystallinity index upon grafting was found from 0.74 to 0.68 for cellulose and grafted Agave cellulose, respectively. Another evidence of grafting showed in the FESEM observation, where the surface of the grafted cellulose was found to be roughed than the raw one.

Comparison of neat and photo-crosslinked polyvinylidene fluoride-co-hexafluoropropylene thin film dielectrics formed by spin-coating

Energy Technology Data Exchange (ETDEWEB)

Iyore, O.D.; Roodenko, K.; Winkler, P.S. [Materials Science and Engineering Department, The University of Texas at Dallas, Richardson, TX 75080 (United States); Noriega, J.R.; Vasselli, J.J. [Electrical Engineering Department, The University of Texas at Tyler, Tyler, TX 75799 (United States); Chabal, Y.J. [Materials Science and Engineering Department, The University of Texas at Dallas, Richardson, TX 75080 (United States); Gnade, B.E., E-mail: gnade@utdallas.edu [Materials Science and Engineering Department, The University of Texas at Dallas, Richardson, TX 75080 (United States)

2013-12-02

We report the characterization of photo-crosslinked polyvinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) thin film, metal–insulator–metal capacitors fabricated using standard semiconductor processing techniques. We characterize the capacitors using in-situ vibrational spectroscopy during thermally-assisted poling and correlate the Fourier transform infrared spectroscopy (FTIR) results with X-ray diffraction (XRD) results. FTIR analysis of the neat PVDF-HFP showed α → β transformations during poling at room temperature and at 55 °C. α → β transformations were observed for the crosslinked polymer only during poling at 55 °C. XRD data revealed that photo-crosslinking caused the polymer to partially crystallize into the β-phase. The similar behavior of the neat and crosslinked samples at 55 °C suggests that a higher activation energy was needed for α → β transformations in crosslinked PVDF-HFP during poling. Electrical measurements showed that photo-crosslinking had no significant effect on the dielectric constant and dielectric loss of PVDF-HFP. However, the dielectric strength and maximum energy density of the crosslinked polymer were severely reduced. - Highlights: • Polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP) dielectrics were studied. • Phase transformations were observed only at 55 °C for the crosslinked PVDF-HFP. • Crosslinking had no strong effect on the dielectric constant of PVDF-HFP. • Breakdown strengths were 620 MVm{sup −1} and 362 MVm{sup −1} for neat and crosslinked films.

Uranium Adsorbent Fibers Prepared by Atom-Transfer Radical Polymerization (ATRP) from Poly(vinyl chloride)- co -chlorinated Poly(vinyl chloride) (PVC- co -CPVC) Fiber

Energy Technology Data Exchange (ETDEWEB)

Brown, Suree; Yue, Yanfeng; Kuo, Li-Jung; Mehio, Nada; Li, Meijun; Gill, Gary; Tsouris, Costas; Mayes, Richard T.; Saito, Tomonori; Dai, Sheng

2016-04-20

The need to secure future supplies of energy attracts researchers in several countries to a vast resource of nuclear energy fuel: uranium in seawater (estimated at 4.5 billion tons in seawater). In this study, we developed effective adsorbent fibers for the recovery of uranium from seawater via atom-transfer radical polymerization (ATRP) from a poly- (vinyl chloride)-co-chlorinated poly(vinyl chloride) (PVC-co-CPVC) fiber. ATRP was employed in the surface graft polymerization of acrylonitrile (AN) and tert-butyl acrylate (tBA), precursors for uranium-interacting functional groups, from PVC-co-CPVC fiber. The [tBA]/[AN] was systematically varied to identify the optimal ratio between hydrophilic groups (from tBA) and uranyl-binding ligands (from AN). The best performing adsorbent fiber, the one with the optimal [tBA]/[AN] ratio and a high degree of grafting (1390%), demonstrated uranium adsorption capacities that are significantly greater than those of the Japan Atomic Energy Agency (JAEA) reference fiber in natural seawater tests (2.42-3.24 g/kg in 42 days of seawater exposure and 5.22 g/kg in 49 days of seawater exposure, versus 1.66 g/kg in 42 days of seawater exposure and 1.71 g/kg in 49 days of seawater exposure for JAEA). Adsorption of other metal ions from seawater and their corresponding kinetics were also studied. The grafting of alternative monomers for the recovery of uranium from seawater is now under development by this versatile technique of ATRP.

Effect of centrifugation and washing on adipose graft viability: a new method to improve graft efficiency.

Science.gov (United States)

Hoareau, Laurence; Bencharif, Karima; Girard, Anne-Claire; Gence, Lydie; Delarue, Pierre; Hulard, Olivier; Festy, Franck; Roche, Regis

2013-05-01

Adipose tissue grafting is a promising method in the field of surgical filling. We studied the effect of centrifugation on fat grafts, and we propose an optimised protocol for the improvement of adipose tissue viability. Adipose tissue was subjected to different centrifugations, and the volumes of interstitial liquid and oil released were measured to choose the optimal condition. Tissue from this condition was then compared to tissue obtained from two traditional techniques: strong centrifugation (commonly 3 min at 3000 rpm/900 g), and decantation, by injecting into immunodeficient mice. The cytokine interleukin-6 (IL-6) and chemokine monocyte chemotactic protein-1 (MCP-1) were assayed 24 h post-injection, and after 1 month of grafting the state of the lipografts was evaluated through macroscopic and histological analysis, with oil gap area measurement. Strong centrifugation (900 g, 1800 g) is deleterious for adipose tissue because it leads to until threefold more adipocyte death compared to low centrifugation (100 g, 400 g). In addition, mice injected with strong centrifuged and non-centrifuged adipose tissue have higher rates of blood IL-6 and MCP-1, compared to those grafted with soft centrifuged fat. Moreover, extensive lipid vacuoles were detectable on histological sections of the non-centrifuged lipografts, whereas lipografts from soft centrifugation contain a higher amount of connective tissue containing collagen fibres. It is necessary to wash and centrifuge adipose tissue before reinjection in order to remove infiltration liquid and associated toxic molecules, which in the long term are deleterious for the graft. However, strong centrifugation is not recommended since it leads very quickly to greater adipocyte death. Thus, soft centrifugation (400 g/1 min), preceded by washings, seems to be the most appropriate protocol for the reinjection of adipose tissue. Copyright © 2013 British Association of Plastic, Reconstructive and Aesthetic Surgeons. Published

Modeling conduction in host-graft interactions between stem cell grafts and cardiomyocytes.

Science.gov (United States)

Chen, Michael Q; Yu, Jin; Whittington, R Hollis; Wu, Joseph C; Kovacs, Gregory T A; Giovangrandi, Laurent

2009-01-01

Cell therapy has recently made great strides towards aiding heart failure. However, while transplanted cells may electromechanically integrate into host tissue, there may not be a uniform propagation of a depolarization wave between the heterogeneous tissue boundaries. A model using microelectrode array technology that maps the electrical interactions between host and graft tissues in co-culture is presented and sheds light on the effects of having a mismatch of conduction properties at the boundary. Skeletal myoblasts co-cultured with cardiomyocytes demonstrated that conduction velocity significantly decreases at the boundary despite electromechanical coupling. In an attempt to improve the uniformity of conduction with host cells, differentiating human embryonic stem cells (hESC) were used in co-culture. Over the course of four to seven days, synchronous electrical activity was observed at the hESC boundary, implying differentiation and integration. Activity did not extend far past the boundary, and conduction velocity was significantly greater than that of the host tissue, implying the need for other external measures to properly match the conduction properties between host and graft tissue.

Preparation of hydrophilic PVDF/PPTA blend membranes by in situ polycondensation and its application in the treatment of landfill leachate

International Nuclear Information System (INIS)

Li, Hongbin; Shi, Wenying; Zhang, Yufeng; Zhou, Rong; Zhang, Haixia

2015-01-01

Graphical abstract: - Highlights: • High modulus PPTA molecules were introduced into PVDF membrane matrix through in situ polycondensation. • Membrane surface hydrophilicity and mechanical strength were improved. • An enhanced antifouling property was obtained when blend membrane was applied in the MBR in the treatment of landfill leachate. • Blend membrane also showed a relatively high removal rate of chemical oxygen demand (COD) and chrom. - Abstract: High modulus poly(p-phenylene terephtalamide) (PPTA) reinforced composites are of great scientific interests. But the thermodynamic difference makes the polymer pairs incompatible and endows the composites with inferior physical-chemical properties. In this study, hydrophilic poly(vinylidene fluoride) (PVDF)/poly(p-phenylene terephtalamide) (PPTA) blend membrane with improved hydrophilicity and mechanical strength was prepared through in situ polycondensation of p-phenylene diamine (PPD) and terephthaloyl chloride (TPC) in PVDF solution and subsequent immersion precipitation phase inversion process. The effects of PPTA concentration in polymer dopes on membrane formation process, structure, morphology and performance were systematically investigated. The results showed that thermodynamically, PPTA acted as a demixing enhancer which accelerated the phase inversion process. Dynamically, liquid-liquid phase separation was still in control of membrane formation process especially in the later period, whereas the addition of PPTA mainly promoted the early emergence of the liquid-liquid demixing. The surface hydrophilicity, ant-fouling properties and mechanical strength were significantly improved when PPTA content was 17 wt%. When PPTA content increased to 26 wt%, membrane bursting pressure increased to nearly 0.6 MPa which was 1.5 times higher than that of PVDF membrane. The resultant PVDF/PPTA blend membrane exhibited an improved antifouling property than that of PVDF membrane when applied in the MBR in the

Preparation of hydrophilic PVDF/PPTA blend membranes by in situ polycondensation and its application in the treatment of landfill leachate

Energy Technology Data Exchange (ETDEWEB)

Li, Hongbin, E-mail: qinyu1105@126.com [School of Textiles Engineering, Henan Institute of Engineering, Zhengzhou, 450007 (China); Shi, Wenying [School of Textiles Engineering, Henan Institute of Engineering, Zhengzhou, 450007 (China); Zhang, Yufeng [State Key Laboratory of Hollow Fiber Membrane Materials and Processes, Tianjin Polytechnic University, Tianjin 300387 (China); Zhou, Rong; Zhang, Haixia [School of Textiles Engineering, Henan Institute of Engineering, Zhengzhou, 450007 (China)

2015-08-15

Graphical abstract: - Highlights: • High modulus PPTA molecules were introduced into PVDF membrane matrix through in situ polycondensation. • Membrane surface hydrophilicity and mechanical strength were improved. • An enhanced antifouling property was obtained when blend membrane was applied in the MBR in the treatment of landfill leachate. • Blend membrane also showed a relatively high removal rate of chemical oxygen demand (COD) and chrom. - Abstract: High modulus poly(p-phenylene terephtalamide) (PPTA) reinforced composites are of great scientific interests. But the thermodynamic difference makes the polymer pairs incompatible and endows the composites with inferior physical-chemical properties. In this study, hydrophilic poly(vinylidene fluoride) (PVDF)/poly(p-phenylene terephtalamide) (PPTA) blend membrane with improved hydrophilicity and mechanical strength was prepared through in situ polycondensation of p-phenylene diamine (PPD) and terephthaloyl chloride (TPC) in PVDF solution and subsequent immersion precipitation phase inversion process. The effects of PPTA concentration in polymer dopes on membrane formation process, structure, morphology and performance were systematically investigated. The results showed that thermodynamically, PPTA acted as a demixing enhancer which accelerated the phase inversion process. Dynamically, liquid-liquid phase separation was still in control of membrane formation process especially in the later period, whereas the addition of PPTA mainly promoted the early emergence of the liquid-liquid demixing. The surface hydrophilicity, ant-fouling properties and mechanical strength were significantly improved when PPTA content was 17 wt%. When PPTA content increased to 26 wt%, membrane bursting pressure increased to nearly 0.6 MPa which was 1.5 times higher than that of PVDF membrane. The resultant PVDF/PPTA blend membrane exhibited an improved antifouling property than that of PVDF membrane when applied in the MBR in the

Modification of macroporous membranes by graft co-polymerization induced by pre-irradiation with an electron accelerator; Modificacion de membranas macroporosas para la recuperacion de protemas por intercambio ionico

Energy Technology Data Exchange (ETDEWEB)

Grasselli, M [Buenos Aires Univ. (Argentina). Facultad de Farmacia y Bioquimica; Yoshii, Fumio [Japan Atomic Energy Research Inst., Takasaki, Gunma (Japan). Takasaki Radiation Chemistry Research Establishment

1999-07-01

Glycidyl methacrylate (GMA) and N,N-dimethylacrylamide (DMAA) have been co-grafted on hollow fiber membranes of macroporous polyethylene. Grafted copolymers have been obtained with different ratios of the monomers (molar ratio between 0 and 2 DMAA/GMA). The properties of the modified membranes are studied.

Platinum/polyaniline transparent counter electrodes for quasi-solid dye-sensitized solar cells with electrospun PVDF-HFP/TiO2 membrane electrolyte

International Nuclear Information System (INIS)

Peng, Shengjie; Li, Linlin; Tan, Huiteng; Srinivasan, Madhavi; Mhaisalkar, Subodh G.; Ramakrishna, Seeram; Yan, Qingyu

2013-01-01

Composite films of platinum and polyaniline (Pt/PANI) with different Pt loadings are prepared by chemical reduction and then a spin-coating process on fluorine-doped tin oxide (FTO) substrates. The obtained Pt/PANI transparent counter electrodes are applied in quasi-solid dye-sensitized solar cells (QDSCs) from front and rear light illuminations, using electrospun poly(vinylidenefluoride-co-hexafluoropropylene)/TiO 2 (PVDF-HFP/TiO 2 ) as the electrolyte. The analytical results show that the 1.8-nm sized Pt nanoparticles are distributed uniformly in the Pt/PANI film when the Pt loading is 1.5 μg cm −2 . Electrocatalytic activity of the Pt/PANI electrode with 1.5 μg cm −2 Pt loading for the I 3 − /I − redox reaction is higher than the conventional sputtered Pt electrode. Furthermore, the mean optical transmittance of the Pt/PANI electrodes is above 60% in the wavelength of 400–800 nm. The optimal QDSC composed of Pt/PANI with 1.5 μg cm −2 Pt loading exhibits power conversion efficiencies of 6.34% and 3.85%, when measured using an AM1.5G solar simulator at 100 mW cm −2 under front and rear light illuminations. The efficiencies are both higher than those of the QDSCs employing the conventional sputtered Pt counter electrode with 8.3 μg cm −2 Pt loading. Moreover, the QDSC exhibits superior long-term stability. These promising results make the potential application of Pt/PANI films as cost-effective, transparent counter electrodes

Obtainment of crotoxin/phema-g-LDPE and crotoxin/PCL systems;Obtencao dos sistemas bioconjugados crotoxina/PEBD-g-phema e crotoxina/PCL

Energy Technology Data Exchange (ETDEWEB)

Lorenzetti, Solange Gubbelini

2006-07-01

The aim of the work was the obtainment of polymeric matrices immobilized with crotoxin purified from crude venom of rattle snake. A matrix was processed by gamma irradiation by the grafting of a hydrogel onto a polymeric film which resulted in a copolymer for the chemical immobilization of crotoxin. The second matrix was attained by the entrapment of crotoxin in microspheres of epsilon-polycaprolactone. After the purification, the crotoxin proceeding from the snake Crotalus durissus terrificus was evaluated biochemical and biologically. The lethal dose (LD50%) of the toxin was 0.09/kg animal. The test of cytotoxicity not revealed any significant difference between the tumoral cells and the respective normal control cells in culture. Grafting copolymers were used as scaffold for the chemical immobilization of the purified crotoxin. For this purpose the low density polyethylene (LDPE) and the hydrophilic monomer 2-hydroxy-ethyl-methacrylate (HEMA) were copolymerized in a {sup 60}Co source. The copolymers (LDPE-g-PHEMA) showed grafting levels in the range of 2 and 50 %. In the infrared spectroscopy analysis (FTIR-ATR) it was observed in the copolymer, carbonyl groups (C=O) and hydroxyl groups -OH due to the grafting of PHEMA. The MEV micrographs showed a smooth surface for the virgin LDPE and a rough surface for the LDPE-g-PHEMA, owing to the presence of grafted PHEMA. The hydrophilicity was observed by the determination of water content in the copolymer after immersion in water. By the diffusion coefficient it was noted that from 30 % grafting degree, the copolymers become less hydrophilic due to the crosslinking increase among the chains in PHEMA. The biocompatibility of the LDPE-g-PHEMA was proved by the cytotoxicity test. At the end, the immobilized copolymer, the entrapped crotoxin and the free crotoxin was tested 'in vivo'. During 20 days, C3H strain mice were observed in their weight, behavior and motor changes. The results demonstrated that the group

Graphene-Silver-Induced Self-Polarized PVDF-Based Flexible Plasmonic Nanogenerator Toward the Realization for New Class of Self Powered Optical Sensor.

Science.gov (United States)

Sinha, Tridib Kumar; Ghosh, Sujoy Kumar; Maiti, Rishi; Jana, Santanu; Adhikari, Basudam; Mandal, Dipankar; Ray, Samit K

2016-06-22

Plasmonic characteristics of graphene-silver (GAg) nanocomposite coupled with piezoelectric property of Poly(vinylidene fluoride) (PVDF) have been utilized to realize a new class of self-powered flexible plasmonic nanogenerator (PNG). A few layer graphene has been prepared in a facile and cost-effective method and GAg doped PVDF hybrid nanocomposite (PVGAg) is synthesized in a one-pot method. The PNG exhibits superior piezoelectric energy conversion efficiency (∼15%) under the dark condition. The plasmonic behavior of GAg nanocomposite makes the PNG highly responsive to the visible light illumination that leads to ∼50% change in piezo-voltage and ∼70% change in piezo-current, leading to enhanced energy conversion efficiency up to ∼46.6%. The piezoelectric throughput of PNG (e.g., capacitor charging performance) has been monitored during the detection of the different wavelengths of visible light illumination and showed maximum selectivity to the green light. The simultaneous mechanical energy harvesting and visible-light detection capabilities of the PNG are attractive for futuristic self-powered optoelectronic smart sensors and devices.

A PVDF-Based Sensor for Internal Stress Monitoring of a Concrete-Filled Steel Tubular (CFST) Column Subject to Impact Loads.

Science.gov (United States)

Du, Guofeng; Li, Zhao; Song, Gangbing

2018-05-23

Impact loads can have major adverse effects on the safety of civil engineering structures, such as concrete-filled steel tubular (CFST) columns. The study of mechanical behavior and stress analysis of CFST columns under impact loads is very important to ensure their safety against such loads. At present, the internal stress monitoring of the concrete cores CFST columns under impact loads is still a very challenging subject. In this paper, a PVDF (Polyvinylidene Fluoride) piezoelectric smart sensor was developed and successfully applied to the monitoring of the internal stress of the concrete core of a CFST column under impact loads. The smart sensor consists of a PVDF piezoelectric film sandwiched between two thin steel plates through epoxy. The protection not only prevents the PVDF film from impact damages but also ensures insulation and waterproofing. The smart sensors were embedded into the circular concrete-filled steel tube specimen during concrete pouring. The specimen was tested against impact loads, and testing data were collected. The time history of the stress obtained from the PVDF smart sensor revealed the evolution of core concrete internal stress under impact loads when compared with the impact force⁻time curve of the hammer. Nonlinear finite element simulations of the impact process were also carried out. The results of FEM simulations had good agreement with the test results. The results showed that the proposed PVDF piezoelectric smart sensors can effectively monitor the internal stress of concrete-filled steel tubular columns under impact loads.

Synthesis of BiVO4-GO-PVDF nanocomposite: An excellent, newly designed material for high photocatalytic activity towards organic dye degradation by tuning band gap energies

Science.gov (United States)

Biswas, Md Rokon Ud Dowla; Oh, Won-Chun

2018-06-01

BiVO4-GO-PVDF (PVDF = Polyvinylidene Difluoride) photocatalyst is successfully synthesized by ultrasonication method and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and transmission electron microscopy techniques. Morphology of BiVO4-GO-PVDF looks like a human embryo embedded inside an amniotic sac. Photocatalytic performance of BiVO4-GO-PVDF for decolorization of methylene blue is investigated. BiVO4-GO-PVDF system reveals enhanced photocatalytic activity degradation of methylene blue (MB), Rhodamine B (RhB) & Safranin-O (SO) in water under visible light irradiation as compared to the pure BiVO4 catalyst, BiVO4 & PTFE decorated on the graphene sheet. The experimental result reveals that the covering of graphene sheets in this composite catalyst enhances photocatalytic performance under visible light. This enhanced activity is mainly attributed to effective quenching of the photogenerated electron-hole pairs confirmed by photoluminescence spectra. Trapping experiments of radicals and holes were conducted to detect reactive species generated in the photocatalytic system, experimental results revealed that direct hole oxidation reaction is obviously dominant during photocatalytic reactions on the BiVO4-GO-PVDF system.

Acrylamide graft over silicone rubber tubes by simultaneous irradiation in 60 Co source

International Nuclear Information System (INIS)

Julio, C.A.; Higa, O.Z.

1992-01-01

The synthesis of a hydrogel having silicone rubber tubes as support was carried out through the radiation grafting technique. The best conditions for the grafting development were determined in relation to the monomer and inhibitor concentration, dose rate and irradiation dose. The addition of cupric ions in the process inhibited the acrylamide homo polymerization and enhanced the grafting yield. The water content in the grafted tubes characterized the hydrophilic property of the material. (author)

Preparation and characterization of acrylic acid-grafted poly (vinyl alcohol) hydrogel actuators using γ-ray irradiation

International Nuclear Information System (INIS)

An, Sung Jun; Lim, Youn Mook; Gwon, Hui Jeong; Kim, Yun Hye; Youn, Min Ho; Nho, Young Chang; Han, Dong Hyun; Kim, Chong Yeal

2008-01-01

Active polymer gels expand and contract in response to certain environmental stimuli, such as the application of an electric field or a change in the pH level of the surroundings. This ability to achieve large, reversible deformations with no external mechanical loading has generated much interest in the use of these gels as biomimetic actuators and artificial muscles. In this study, poly (vinyl alcohol)(PVA) grafted acrylic acid monomer (PVA-g-AAc) hydrogels were prepared by 60 Co γ-ray irradiation and their properties such as degree of grafting and weight swelling in electrostimulation as an artificial muscle and actuator were investigated

Excellent Aesthetic and Functional Outcome After Fractionated Carbon Dioxide Laser Skin Graft Revision Surgery: Case Report and Review of Laser Skin Graft Revision Techniques.

Science.gov (United States)

Ho, Derek; Jagdeo, Jared

2015-11-01

Skin grafts are utilized in dermatology to reconstruct a defect secondary to surgery or trauma of the skin. Common indications for skin grafts include surgical removal of cutaneous malignancies, replacement of tissue after burns or lacerations, and hair transplantation in alopecia. Skin grafts may be cosmetically displeasing, functionally limiting, and significantly impact patient's quality-of-life. There is limited published data regarding skin graft revision to enhance aesthetics and function. Here, we present a case demonstrating excellent aesthetic and functional outcome after fractionated carbon dioxide (CO2) laser skin graft revision surgery and review of the medical literature on laser skin graft revision techniques.

Piezoelectric PVDF materials performance and operation limits in space environments

International Nuclear Information System (INIS)

Dargaville, Tim Richard; Assink, Roger Alan; Clough, Roger Lee; Celina, Mathias Christopher

2004-01-01

Piezoelectric polymers based on polyvinylidene fluoride (PVDF) are of interest for large aperture space-based telescopes. Dimensional adjustments of adaptive polymer films are achieved via charge deposition and require a detailed understanding of the piezoelectric material responses which are expected to suffer due to strong vacuum UV, gamma, X-ray, energetic particles and atomic oxygen under low earth orbit exposure conditions. The degradation of PVDF and its copolymers under various stress environments has been investigated. Initial radiation aging studies using gamma- and e-beam irradiation have shown complex material changes with significant crosslinking, lowered melting and Curie points (where observable), effects on crystallinity, but little influence on overall piezoelectric properties. Surprisingly, complex aging processes have also been observed in elevated temperature environments with annealing phenomena and cyclic stresses resulting in thermal depoling of domains. Overall materials performance appears to be governed by a combination of chemical and physical degradation processes. Molecular changes are primarily induced via radiative damage, and physical damage from temperature and AO exposure is evident as depoling and surface erosion. Major differences between individual copolymers have been observed providing feedback on material selection strategies

High fluorescence emission silver nano particles coated with poly (styrene-g-soybean oil) graft copolymers: Antibacterial activity and polymerization kinetics.

Science.gov (United States)

Hazer, Baki; Kalaycı, Özlem A

2017-05-01

Autoxidation of poly unsaturated fatty acids makes negative effect on foods. In this work, this negative effect was turned to a great advantage using autoxidized soybean oil as a macroperoxide nanocomposite initiator containing silver nano particles in free radical polymerization of vinyl monomers. The synthesis of soybean oil macro peroxide was carried out by exposing soybean oil to air oxygen with the presence of silver nanoparticles (Ag NPs) at room temperature. Autoxidized soybean oil macroperoxide containing silver nanoparticles (Agsbox) successfully initiated the free radical polymerization of styrene in order to obtain Polystyrene (PS)-g-soybean oil graft copolymer containing Ag NPs. Both autoxidized soybean oil and PS-g-sbox with Ag NPs showed a surface plasmon resonance and high fluorescence emission. Overall rate constant (K) of styrene polymerization initiated by autoxidized soybean oil macroperoxide with Ag NPs was found to be K=1.95.10 -4 Lmol -1 s -1 at 95°C. Antibacterial efficiency was observed in the PS-g-soybean oil graft copolymer film samples containing Ag NPs. 1 H NMR and GPC techniques were used for the structural analysis of the fractionated polymeric oils. Copyright © 2016 Elsevier B.V. All rights reserved.

SC-CO2-assisted process for a high energy density aerogel supercapacitor: the effect of GO loading

Science.gov (United States)

Sarno, Maria; Baldino, Lucia; Scudieri, Carmela; Cardea, Stefano; Ciambelli, Paolo; Reverchon, Ernesto

2017-05-01

Energy density, safety, and simple and environmentally friendly preparation methods are very significant aspects in the realization of a compact supercapacitor. Herein we report the use of a supercritical CO2-assisted gel drying process (SC-CO2) for the preparation of porous electrodes containing dispersed graphene in a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) binder membrane to sandwich in a new portable supercapacitor based on graphene oxide (GO). A GO loading of 60 wt.% was found to give the best combination of factors (porosity, wettability, mechanical and electrochemical properties). Cycling voltammetry and charge/discharge studies showed an excellent capacitance behaviour and stability in an ionic liquid electrolyte, suggesting SC-CO2 processing as a promising platform to produce highly bulky and porous films for supercapacitors. The supercapacitor device delivers a very high energy density of 79.2 Wh kg-1 at a power density of 0.23 KW kg-1 (current density 0.5 A g-1, specific capacitance 36.2 F g-1) while that of steel remains at 50.3 Wh kg-1 at a power density of 2.8 KW kg-1 (current density 6 A g-1, specific capacitance 23.5 F g-1).

Grafting functional antioxidants on highly crosslinked polyethylene

Science.gov (United States)

Al-Malaika, S.; Riasat, S.; Lewucha, C.

2016-05-01

The problem of interference of antioxidants, such as hindered phenols, with peroxide-initiated crosslinking of polyethylene was addressed through the use of functional (reactive) graftable antioxidants (g-AO). Reactive derivatives of hindered phenol and hindered amine antioxidants were synthesised, characterised and used to investigate their grafting reactions in high density polyethylene; both non-crosslinked (PE) and highly peroxide-crosslinked (PEXa). Assessment of the extent of in-situ grafting of the antioxidants, their retention after exhaustive solvent extraction in PE and PEXa, and the stabilising performance of the grafted antioxidants (g-AO) in the polymer were examined and benchmarked against conventionally stabilised crosslinked & non-crosslinked polyethylene. It was shown that the functional antioxidants graft to a high extent in PEXa, and that the level of interference of the g-AOs with the polymer crosslinking process was minimal compared to that of conventional antioxidants which bear the same antioxidant function. The much higher level of retention of the g-AOs in PEXa after exhaustive solvent extraction, compared to that of the corresponding conventional antioxidants, accounts for their superior long-term thermal stabilising performance under severe extractive conditions.

Modification of polyetherurethane for biomedical application by radiation-induced grafting. I. Grafting procedure, determination of mechanical properties, and chemical modification of grafted films

International Nuclear Information System (INIS)

Jansen, B.; Ellinghorst, G.

1985-01-01

Radiation grafting of monomers onto suitable trunk polymers is a useful tool for tailoring new polymers for special purposes. This technique has been used in the past for the development of biocompatible materials, e.g., by grafting hydrogels onto mechanically stable polymers. In this first part of our work, the radiation grafting of hydrophilic or reactive monomers onto a polyetherurethane film using the pre-swelling technique is described. Following this technique the trunk polymer was swollen in the monomer before irradiation. As monomers 2-hydroxyethyl methacrylate (HEMA), 2,3-epoxypropyl methacrylate (GMA), 2,3-dihydroxypropyl methacrylate (GOMA), and acrylamide (AAm) were used. The kinetics of the grafting reactions were examined, and the distribution of the graft component inside the trunk polymer was investigated by means of infrared (IR) spectroscopy. Surface-grafted as well as bulk- and surface-grafted products could be obtained. The mechanical behavior of the grafted films--especially in the water-swollen state--was examined and compared with that of the pure trunk polymer. In nearly all cases it was found that the tensile strength sigma B and the elongation at break epsilon R decreases as the grafting yield increases. Modification of GMA- and AAm-grafted films via chemical reactions was performed to create new functional groups of biomedical interest. In this manner a diol structure, a carboxylic acid structure, and a sulfonic acid group could be introduced in the grafted polymer. The water uptake of such modified films is increased markedly when compared with that of the unmodified samples

Polymer foam comprising a polymer and nanoparticles, and nanoparticles for the manufacture of such foam.

NARCIS (Netherlands)

Vancso, Gyula J.; Duvigneau, Joost; Nederkoorn, P.H.J.; Wassing, T.

2014-01-01

A polymer foam is produced comprising a polymer and nanoparticles having a maximum dimensionof 750 nm, which foam has cells with an average cell size of at most 1 µm and a cell density of at least 1012 cells/ml, wherein polymeric grafts have been attached to the nanoparticles. The nanoparticles may

NaCl leached sustainable porous flexible Fe3O4 decorated RGO-polyaniline/PVDF composite for durable application against electromagnetic pollution

Directory of Open Access Journals (Sweden)

R. Bera

2017-05-01

Full Text Available To avoid the interference of electromagnetic radiation from other devices, an electronic device needs to be fabricated with flexible and light weight electromagnetic interference (EMI shielding materials with high efficiency. According, highly flexible porous poly(vinylidene fluoride (PVDF/PFR (Fe3O4 decorated polyaniline/RGO composite composite was prepared through solution blending of PVDF with pre-synthesized PFR conductive composite that involves in-situ oxidative polymerization of aniline in the presence of reduced graphene oxide (RGO using FeCl3 as oxidant. The porous morphology of the composite was created by leaching out of mixed NaCl from the composite. Polyaniline and RGO were mutually decorated by chemically in-situ synthesized ferrosoferric oxide (Fe3O4 using the Fe source of FeCl3. A homogeneous dispersion of PFR in insulated PVDF matrix resulted in a highly electrical conductive composite (PVDF-PFR material through formation of three dimensional continuous conductive networks of polyaniline-RGO in the matrix phase. The composite shows an outstanding EMI shielding effectiveness (EMI SE property due to the porous structure and the presence of conductive network and ferromagnetic Fe3O4 nanoparticles. The PVDF-PFR composite (0.5 mm thickness depicts a great permittivity and permeability value and achieve high EMI SE value (≈–28.18 dB and conductivity value of ≈1.10·10–1 S·cm–1 at very low loading (5 wt% of RGO.

Methodological development and characterization of welded joints in Poly (vinylidene fluoride) (PVDF)

International Nuclear Information System (INIS)

Cedrola, S.M.L.; Costa, M.F. da; Pasqualino, I.P.

2010-01-01

Pipelines are of great concern in the transport sector of oil and gas industries, mainly due to the natural internal aging process caused by contact with the different transported fluids. Installation of polymeric pipes called liners is a good option for rehabilitation of long segments of deteriorated pipelines. Among the potential materials for such application is Poly (vinylidene fluoride) (PVDF). Meanwhile the installation process cannot be carried out in one single step and the polymeric pipe must be cut in sections that are welded during the installation process. In this research welding methodology was studied aiming to optimize welding conditions and the mechanical properties of the joined materials. The first step was processing the PVDF via compression molding on different conditions. Then, the sample was cut and butt-welded. Welding parameters such as, time control, temperature and contact pressure were studied. Afterwards, the stress-strain properties of the welded material was evaluated and physical characterization was carried by x-ray diffraction (DRX). (author)

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. Copyright © 2016 Elsevier B.V. All rights reserved.

Effect of acid additives on graft copolymerization and water absorption of graft copolymers of cassava starch and acrylamide/acrylic acid

International Nuclear Information System (INIS)

Kiatkamjornwong, Suda; Mongkolsawat, Kanlaya; Sonsuk, Manit

2003-01-01

Gelatinized cassava starch was radiation graft copolymerized with acrylamide or acrylic acid in the presence of sulfuric acid, nitric acid or maleic acid at a specific dose rate to a fixed total dose. Homopolymer or free copolymer was extracted by water to obtain the pure graft copolymer, which was subsequently saponified with 5% potassium hydroxide solution at room temperature for 90 min. The saponified graft copolymer was investigated for the effect of acid additives and water absorption. The addition of 2% maleic acid into the grafting reaction containing acrylamide-to-starch ratio of 2.5:1 can produce the superabsorbent copolymer having water absorption as high as 2,256 ± 25 g g -1 . The effect of acid additive was explained. (author)

Enhanced removal of nitrate from water using amine-grafted agricultural wastes

Energy Technology Data Exchange (ETDEWEB)

Kalaruban, Mahatheva; Loganathan, Paripurnanda [Faculty of Engineering, University of Technology Sydney (UTS), P.O. Box 123, Broadway, NSW 2007 (Australia); Shim, W.G. [Faculty of Engineering, University of Technology Sydney (UTS), P.O. Box 123, Broadway, NSW 2007 (Australia); Department of Polymer Science and Engineering, Sunchon National University, 255 Jungang-ro, Suncheon, Jeollanam-do (Korea, Republic of); Kandasamy, Jaya; Ngo, H.H. [Faculty of Engineering, University of Technology Sydney (UTS), P.O. Box 123, Broadway, NSW 2007 (Australia); Vigneswaran, Saravanamuthu, E-mail: s.vigneswaran@uts.edu.au [Faculty of Engineering, University of Technology Sydney (UTS), P.O. Box 123, Broadway, NSW 2007 (Australia)

2016-09-15

Adsorption using low-cost adsorbents is a favourable water treatment method for the removal of water contaminants. In this study the enhanced removal of nitrate, a contaminant at elevated concentration affecting human health and causing eutrophication of water, was tested using chemically modified agricultural wastes as adsorbents. Batch and fixed-bed adsorption studies were performed on corn cob and coconut copra that were surface modified by amine-grafting to increase the surface positive charges. The Langmuir nitrate adsorption capacities (mg N/g) were 49.9 and 59.0 for the amine-grafted (AG) corn cob and coconut copra, respectively at pH 6.5 and ionic strength 1 × 10{sup −3} M NaCl. These values are higher than those of many commercially available anion exchange resins. Fixed-bed (15-cm height) adsorption capacities (mg N/g) calculated from the breakthrough curves were 15.3 and 18.6 for AG corn cob and AG coconut copra, respectively, for an influent nitrate concentration 20 mg N/L at a flow velocity 5 m/h. Nitrate adsorption decreased in the presence of sulphate, phosphate and chloride, with sulphate being the most competitive anion. The Thomas model fitted well to the fixed-bed adsorption data from four repeated adsorption/desorption cycles. Plug-flow model fitted well to the data from only the first cycle. - Highlights: • Ground coconut copra and corn cob particles surfaces are readily amine-grafted. • Amine-grafting reversed the particles' surface charge from negative to positive. • Amine-grafting of the waste particles increased nitrate adsorption capacity. • Nitrate adsorption capacity reduced by co-ions; sulphate > chloride > phosphate. • Fixed-bed nitrate adsorption data fitted well to Thomas and plug-flow models.

Enhanced removal of nitrate from water using amine-grafted agricultural wastes

International Nuclear Information System (INIS)

Kalaruban, Mahatheva; Loganathan, Paripurnanda; Shim, W.G.; Kandasamy, Jaya; Ngo, H.H.; Vigneswaran, Saravanamuthu

2016-01-01

Adsorption using low-cost adsorbents is a favourable water treatment method for the removal of water contaminants. In this study the enhanced removal of nitrate, a contaminant at elevated concentration affecting human health and causing eutrophication of water, was tested using chemically modified agricultural wastes as adsorbents. Batch and fixed-bed adsorption studies were performed on corn cob and coconut copra that were surface modified by amine-grafting to increase the surface positive charges. The Langmuir nitrate adsorption capacities (mg N/g) were 49.9 and 59.0 for the amine-grafted (AG) corn cob and coconut copra, respectively at pH 6.5 and ionic strength 1 × 10"−"3 M NaCl. These values are higher than those of many commercially available anion exchange resins. Fixed-bed (15-cm height) adsorption capacities (mg N/g) calculated from the breakthrough curves were 15.3 and 18.6 for AG corn cob and AG coconut copra, respectively, for an influent nitrate concentration 20 mg N/L at a flow velocity 5 m/h. Nitrate adsorption decreased in the presence of sulphate, phosphate and chloride, with sulphate being the most competitive anion. The Thomas model fitted well to the fixed-bed adsorption data from four repeated adsorption/desorption cycles. Plug-flow model fitted well to the data from only the first cycle. - Highlights: • Ground coconut copra and corn cob particles surfaces are readily amine-grafted. • Amine-grafting reversed the particles' surface charge from negative to positive. • Amine-grafting of the waste particles increased nitrate adsorption capacity. • Nitrate adsorption capacity reduced by co-ions; sulphate > chloride > phosphate. • Fixed-bed nitrate adsorption data fitted well to Thomas and plug-flow models.

Preparation and characterization of polymer nanocomposites based on PVDF/PVC doped with graphene nanoparticles

Directory of Open Access Journals (Sweden)

I.S. Elashmawi

Full Text Available Novel nanocomposites based on PVDF/PVC blend containing graphene oxide nanoparticles (GO were prepare using sonicator. IR analysis revealed that the addition of GO prompts a crystal transformation of α-phase of PVDF. The change of the structural before and after adding GO to PVDF/PVC were studied by X-ray diffraction. A decrease in activation energy gap from UV data was observed with increasing GO content, implying a variation of reactivity as a result of reaction extent. The variation of ε′ with frequency is nearly the same as that of ε″. At higher frequencies, the decrease of both ε′ and ε″ becomes nearly constant. The dispersion at lower frequencies ε′ of ε′ polarization is of Maxwell–Wagner interfacial polarization but at higher frequencies, it levels off. The behavior of conductivity (σAC tends to acquire constant values approaching it DC values. The values of σAC was increased after doped GO with exponential increase after the critical value of frequency. All nanocomposites behaved the same fashion revealing that a higher number of polarons were getting added to conducting pool in composites as graphene content was increased. Conduction mechanism appeared to be getting expedited with increasing frequency due to fact that increase in frequency enhances polaron hopping frequency. Keywords: Nanocomposites, Graphene oxide, FT-IR, X-ray, AC conductivity

Enhanced discharge energy density of rGO/PVDF nanocomposites: The role of the heterointerface

Science.gov (United States)

Zhang, Ye; Wang, Yaqiong; Qi, Shaojun; Dunn, Steve; Dong, Hanshan; Button, Tim

2018-05-01

Recent reports of conductive-filler/polymer composites with large dielectric permittivity (K) make them potential candidates for flexible capacitors. Hence, an interesting question is how these high K composites behave under a strong electric field strength. In this letter, we use in-situ-reduced graphite oxide (rGO)/poly(vinylidene fluoride) (PVDF) nanocomposites as an example to study the energy storage behaviour of high K materials. We show the dielectric behaviour contrasts between weak and strong fields. High K materials inevitably become more lossy with increasing field strength. Simultaneously, we reveal that the in-situ reduction temperature can affect the energy storage performance. Improved energy storage performance is achieved for a nanocomposite reduced at a moderate temperature. When reduced at 160 °C, a device with an rGO volume fraction of 1.5 vol. % displayed a discharge energy density of 0.67 J/cm3 at 50 MV/m. This was 2.9 times greater than pure PVDF. We develop a model to explain this behaviour that proposes a reduced electrical contrast of the rGO/PVDF heterointerface minimising the recombination of localized charge carriers. Our results indicate, simultaneously, the potential and limitation of high K nanocomposites and shed light on the optimisation of the design and fabrication of high discharge energy density flexible capacitors for microelectronic devices.

Study of β-phase development in spin-coated PVDF thick films

Indian Academy of Sciences (India)

2017-06-09

Jun 9, 2017 ... C and increase in spin speed increases the β-phase ... extensively used in the field of sensors and actuators [1–8]. ... some methods to achieve these polar phases in PVDF such as ... ites with materials, such as, gold nanoparticles [14], carbon ..... change in degree of crystallinity of the films subject to the ...

Transport Properties, Mechanical Behavior, Thermal and Chemical Resistance of Asymmetric Flat Sheet Membrane Prepared from PSf/PVDF Blended Membrane on Gauze Supporting Layer

Directory of Open Access Journals (Sweden)

Nita Kusumawati

2018-05-01

Full Text Available Asymmetric polysulfone (PSf membrane is prepared using phase inversion method and blending with polyvinylidene fluoride (PVDF on the gauze solid support. Casting solution composition optimization has been done to get PSf/PVDF membrane with best characteristics and permeability. The result shows that blending on PSf with PVDF polymer using phase inversion method has been very helpful in creating an asymmetric porous membrane. Increased level of PVDF in casting solution has increased the formation of asymmetry structure and corresponding flux membrane. The result from thermal test using Differential Scanning Calorimetry (DSC-Thermal Gravimetric Analysis (TGA shows the resistance of the membrane to temperature 460 °C. Membrane resistance against acid looks from undetectable changes on infrared spectra after immersion process in H2SO4 6–98 v/v%. While membrane color changes from white to brownish and black is detected after the immersion process in sodium hydroxide (NaOH 0.15–80 w/v%.

Palladium catalyst system comprising zwitterion and/or acid-functionalized ionic liquid

DEFF Research Database (Denmark)

2011-01-01

The present invention concerns a catalyst system in particular a catalyst system comprising Palladium (Pd), a zwitterion and/or an acid-functionalized ionic liquid, and one or more phosphine ligands, wherein the Pd catalyst can be provided by a complex precursor, such as Pd(CH3COO)2, PdCI2, Pd(CH3......COCHCOCH3), Pd (CF3COO)2, Pd(PPh3)4 or Pd2(dibenzylideneacetone)3. Such catalyst systems can be used for e.g. alkoxycarbonylation reactions, carboxylation reactions, and/or in a co-polymerization reaction, e.g. in the production of methyl propionate and/or propanoic acid, optionally in processes forming...... methyl methacrylate and/or methacrylic acid. Catalyst systems according to the invention are suitable for reactions forming separable product and catalyst phases and supported ionic liquid phase SILP applications....

EFFECT OF DEXTRAN-graft-POLYACRYLAMIDE INTERNAL STRUCTURE ON FLOCCULATION PROCESS PARAMETERS

International Nuclear Information System (INIS)

Bezugla, T.; Kutsevol, N.; Shyichuk, A.; Ziolkowska, D.

2008-01-01

Dextran-graft-Polyacrylamide copolymers (D-g-PAA) of brush-like architecture were tested as flocculation aids in the model kaolin suspensions. Due to expanded conformation the D-g-PAA copolymers are more effective flocculants than individual PAA with close molecular mass. The internal structure of D-g-PAA copolymers which is determined by number and length of grafted PAA chains, the distance between grafts, etc., has the significant influence on flocculation behavior of such polymers

Bone formation in cranial, mandibular, tibial and iliac bone grafts in rats

DEFF Research Database (Denmark)

Solheim, E; Pinholt, E M; Talsnes, O

1995-01-01

Several studies have suggested that grafts from membranous derived bone (e.g., calvarial grafts) retain their volume better than those from endochondral derived bone (e.g., iliac bone grafts). Increased osteogenesis in grafts of the former type has been offered as the explanation. However, simple...... volume measurements of the recovered grafts do not differentiate between viable and dead bone. We studied fresh syngeneic full-thickness bone grafts from calvaria, mandibula, tibia diaphysis, and iliac bone implanted in the back muscles of young Lewis rats. Bone formation in grafts recovered 3 weeks...... that the anatomical area of harvest is important regarding new bone formation in syngeneic bone grafts. However, the results do not support the contention that better maintenance of volume of calvarial grafts compared with iliac bone grafts is due to enhanced osteogenesis in the former....

Influence of the dose rate in the PVDF degradation processes

Energy Technology Data Exchange (ETDEWEB)

Batista, Adriana S.M.; Pereira, Claubia, E-mail: adriananuclear@yahoo.com.br, E-mail: claubia@nuclear.ufmg.br [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil); Gual, Maritza R., E-mail: maritzargual@gmail.com [Instituto Superior de Tecnologias y Ciencias Aplicadas (InsTEC), Departamento de Ingenieria Nuclear, La Habana (Cuba); Faria, Luiz O., E-mail: farialo@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

2015-07-01

Modification in polymeric structure of plastic material can be brought either by conventional chemical means or by exposure to ionization radiation from gamma radioactive sources or highly accelerated electrons. The prominent drawbacks of chemical cross-linking typically involve the generation by products such as peroxide degradation. Radiation cross-linking technologies include: application in cable and wire, application in rubber tyres, radiation vulcanization of rubber latex, polymer recycling, hydrogels etc. The degradation of PVDF polymer exposed to gamma irradiation in oxygen atmosphere in high dose rate has been studied and compared to obtained under smaller dose rates. The samples were irradiated with a Co-60 source at constant dose rate (12 kGy/h and 2,592 kGy/h), with doses ranging from 100 kGy to 3,000 kGy. Different dose rate determine the prevalence of the processes being evaluated in this work by thermal measurements and infrared spectroscopy. It is shown that the degradation processes involve chain scissions and crosslink formation. The formation of oxidation products was shown at the surface of the irradiated film. The FTIR data revealed absorption bands at 1730 and 1853 cm{sup -1} which were attributed to the stretch of C=O bonds, at 1715 and 1754 cm{sup -1} which were attributed to the C=C stretching and at 3518, 3585 and 3673 cm{sup -1} which were associated with NH stretch of NH{sub 2} and OH. Thermogravimetric studies reveal that the irradiation induced the increasing residues and decrease of the temperature of the decomposition start. (author)

Influence of the dose rate in the PVDF degradation processes

International Nuclear Information System (INIS)

Batista, Adriana S.M.; Pereira, Claubia; Gual, Maritza R.; Faria, Luiz O.

2015-01-01

Modification in polymeric structure of plastic material can be brought either by conventional chemical means or by exposure to ionization radiation from gamma radioactive sources or highly accelerated electrons. The prominent drawbacks of chemical cross-linking typically involve the generation by products such as peroxide degradation. Radiation cross-linking technologies include: application in cable and wire, application in rubber tyres, radiation vulcanization of rubber latex, polymer recycling, hydrogels etc. The degradation of PVDF polymer exposed to gamma irradiation in oxygen atmosphere in high dose rate has been studied and compared to obtained under smaller dose rates. The samples were irradiated with a Co-60 source at constant dose rate (12 kGy/h and 2,592 kGy/h), with doses ranging from 100 kGy to 3,000 kGy. Different dose rate determine the prevalence of the processes being evaluated in this work by thermal measurements and infrared spectroscopy. It is shown that the degradation processes involve chain scissions and crosslink formation. The formation of oxidation products was shown at the surface of the irradiated film. The FTIR data revealed absorption bands at 1730 and 1853 cm -1 which were attributed to the stretch of C=O bonds, at 1715 and 1754 cm -1 which were attributed to the C=C stretching and at 3518, 3585 and 3673 cm -1 which were associated with NH stretch of NH 2 and OH. Thermogravimetric studies reveal that the irradiation induced the increasing residues and decrease of the temperature of the decomposition start. (author)

Magnetic, dielectric and magnetodielectric properties of PVDF-La0.7Sr0.3MnO3 polymer nanocomposite film

Directory of Open Access Journals (Sweden)

Ch. Thirmal

2013-11-01

Full Text Available We have investigated the structure, magnetic and dielectric properties of PVDF-La0.7Sr0.3MnO3 polymer nanocomposite thick film fabricated by dip coating technique along with the magnetodielectric effect. The structure and dielectric properties show the enhanced β phase in the composite compared to the PVDF film. The coupling between the ferroelectric and magnetic phases in the composite is revealed in the form of dielectric anomaly at the ferromagnetic Curie temperature. We observed 1.9% magnetodielectric effect at 300 K with the possibility of enhanced effect near the transition temperature. In addition, the analysis of the electric modulus indicates that the composite exhibits interfacial related relaxation and it follows Arrhenius Law. Our study suggests that the ac conductivity of the PVDF-La0.7Sr0.3MnO3 composite could be explained by correlated barrier hopping mechanism.

Enhanced bacterial affinity of PVDF membrane: its application as improved sea water sampling tool for environmental monitoring.

Science.gov (United States)

Kumar, Sweta Binod; Sharnagat, Preeti; Manna, Paramita; Bhattacharya, Amit; Haldar, Soumya

2017-02-01

Isolation of diversified bacteria from seawater is a major challenge in the field of environmental microbiology. In the present study, an attempt has been made to select specific membrane with improved property of attaching diversified bacteria. Initially, different concentrations (15, 18, and 20% W/W) of polysulfone (PSF) were used to check their affinity for the attachment of selected gram-positive (Bacillus subtilis) and gram-negative (Escherichia coli) bacteria. Among these, 20% W/W PSF showed maximum attachment. Therefore, membrane prepared with other materials such as polyvinylidene fluoride (PVDF) and polyether sulfone (PES) were used with the same concentration (20% W/W) to check their improved bacterial attachment property. Comparative study of bacterial attachment on three different membranes revealed that PVDF possessed the highest affinity towards both the groups of bacteria. This property was confirmed by different analytical methods viz. contact angle, atomic force microscopy, zeta potential, and flux study and further validated with seawater samples collected from seven sites of western coast and Lakshadweep island of India, using Biolog EcoPlate™. All the samples showed that bacterial richness and diversity was high in PVDF membrane in comparison to surrounding seawater samples. Interestingly, affinity for more diversified bacteria was reported to be higher in water sample with less turbidity and low bacteria load. This finding can facilitate the development of PVDF (20% W/W) membrane as a simple, cheap, and less labor intensive environmental sampling tool for the isolation of diversified bacteria from seawater sample wih different physiochemical properties. Graphical abstract ᅟ.

Preparation and characterization of novel PVDF nanofiltration membranes with hydrophilic property for filtration of dye aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Nikooe, Naeme, E-mail: naeme.nikooe@stu.um.ac.ir; Saljoughi, Ehsan, E-mail: saljoughi@um.ac.ir

2017-08-15

Highlights: • Preparation of novel PVDF nanofiltration membranes with noticeable hydrophilicity. • Simultaneous achievement of hydrophilicity and dye removal via addition of Brij-58. • In situ modification and stability of hydrophilic property via addition of Brij-58. - Abstract: In the present research, for the first time PVDF/Brij-58 blend nanofiltration membranes with remarkable performance in filtration of dye aqueous solution were prepared via immersion precipitation. A noticeable improvement in water permeation and fouling resistance of the PVDF membranes was achieved by using Brij-58 surfactant as a hydrophilic additive. Scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FT-IR) and water contact angle were applied for the investigation of membrane morphology, detection of the surface chemical composition and relative hydrophilicity/hydrophobicity, respectively. The membrane performance was studied and compared by determination of pure water flux (PWF) and filtration of synthetic reactive dye aqueous solutions as well as bovine serum albumin (BSA) as foulant model. It was found out that addition of 4 wt.% Brij-58 to the casting solution results in formation of membrane with remarkable hydrophilicity and fouling resistance (contact angle of 46° and flux recovery ratio (FRR) = 90%), higher porosity and consequently noticeable PWF (31.2 L/m{sup 2} h) and recognized dye rejection value (90%) in comparison with the pristine PVDF nanofiltration membrane. Addition of Brij-58 surfactant to the casting solution resulted in formation of NF membrane with higher hydrophilicity and permeability as well as higher dye rejection value in comparison with the addition of PEG 400 additive.

Ionic properties of non-aqueous liquid and PVDF-based gel electrolytes containing a cesium thiolate/disulfide redox couple

International Nuclear Information System (INIS)

Renard, Ingrid; Li Hongmei; Marsan, Benoit

2003-01-01

Liquid electrolytes containing a cesium thiolate/disulfide redox couple, prepared from 5-mercapto-1-methyltetrazole cesium salt (CsT) and di-5-(1-methyltetrazole)disulfide (T 2 ) dissolved in several aprotic solvents and solvent mixtures, have been studied using various techniques. FTIR spectroscopy reveals that relatively strong interactions occur between the reduced species T - and DMSO or DMF while Cs + ions are very weakly coordinated to the S=O or C=O bond. It is shown that the electrolyte consisting of 1.55 mol kg -1 CsT in the solvent mixture DMSO/DMF (40/60%) exhibits the highest conductivity (1.1x10 -2 and 2.3x10 -2 S cm -1 at 23 and 80 deg. C, respectively), and that the presence of the oxidized species T 2 does not affect significantly its electrical properties up to a CsT:T 2 molar ratio of 5:1. Conductivity values as a function of salt concentration are discussed in terms of the effective number of charge carriers, taking into account the level of ionic association, and of the ionic mobility. Optically transparent gel electrolytes have been prepared by incorporation of the optimal liquid electrolyte into various amounts of poly(vinylidene fluoride) (PVDF). It is shown that ionic mobility is not much affected by the polymer concentration, suggesting that migration of ions occurs mainly through the solvent mixture surrounded by the PVDF matrix

Development of thermoresponsive poly(propylene-g-N-isopropylacrylamide) non-woven 3D scaffold for smart cell culture using oxyfluorination-assisted graft polymerisation

CSIR Research Space (South Africa)

Chetty, AS

2013-02-01

Full Text Available using oxyfluorination-assisted graft polymerisation (OAGP). New polar functional groups were detected on the oNWF, and PNIPAAm was confirmed in the gNWF by attentuated total-reflectance Fourier transform infrared (ATR-FTIR) and scanning X...

Synthesis of co-polymer-grafted gum karaya and silica hybrid organic–inorganic hydrogel nanocomposite for the highly effective removal of methylene blue

CSIR Research Space (South Africa)

Mittal, H

2015-11-01

Full Text Available The aim of this work was to study the adsorption behavior of the nanosilica-containing hydrogel nanocomposite of gum karaya grafted with poly(acrylic acid-acrylamide) (GK-cl-P(AA-co-AAM)) in the adsorption of methylene blue (MB) from aqueous...

Biodegradable flocculants based on polyacrylamide and poly(N,N-dimethylacrylamide) grafted amylopectin.

Science.gov (United States)

Kolya, Haradhan; Tripathy, Tridib

2014-09-01

Synthesis of amylopectin grafted polyacrylamide (AP-g-PAM) and poly(N,N-dimethylacrylamide) (AP-g-PDMA) was carried out by Ce4+ in water medium. The reaction conditions for maximum grafting was optimized by varying the reaction variables, including the concentration of monomers, ceric ammonium nitrate (CAN), amylopectin, reaction time and temperature. The graft copolymers were characterized by FTIR spectroscopy, NMR (both 1H and 13C) spectroscopy, molecular weight determination and molecular weight distribution by using size exclusion chromatography (SEC), thermal analysis (TGA), SEM studies. Biodegradation of the graft copolymers was carried out by enzyme hydrolysis. Flocculation performances of the graft copolymers were evaluated in 1.0 wt% coal and 1.0 wt% silica suspensions. A comparative study of the flocculation performances of AP-g-PDMA and AP-g-PAM was also made. It shows that the flocculation performance of AP-g-PDMA was better than that of AP-g-PAM. AP-g-PDMA performed best when compared with other commercial flocculants in the same suspensions. Copyright © 2014 Elsevier B.V. All rights reserved.

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

International Nuclear Information System (INIS)

Klinpituksa, P; Kongkalai, P; Kaesaman, A

2014-01-01

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

Effects of water on starch-g-polystyrene and starch-g-poly(methyl acrylate) extrudates

International Nuclear Information System (INIS)

Henderson, A.M.; Rudin, A.

1982-01-01

Polystyrene and poly(methyl acrylate) were grafted onto wheat starch by gamma radiation and chemical initiation, respectively. The respective percent add-on values were 46 and 45; 68% of the polystyrene formed was grafted to starch, and corresponding proportion of poly(methyl acrylate) was 41%. The molecular weight distributions of the homopolymer and graft portions were characterized, and extrusion conditions were established for production of ribbon samples of starch-g-PS and starch-g-PMA. Both copolymer types were considerably weakened by soaking in water, and this effect was more immediate and drastic for starch-g-poly(methyl acrylate). Both graft copolymers regained their original tensile strengths on drying, but the poly(methyl acrylate) specimens did not recover their original unswollen dimensions and retained high breaking elongations characteristic of soaked specimens. Tensile and dynamic mechanical properties of extruded and molded samples of both graft polymers are reported, and plasticizing effects of water are summarized

Preparation of vinyl acetate grafted natural rubber by irradiation method