首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
    
Studies on the relationship between resistivity and dynamic rheological properties of carbon black‐filled high‐density polyethylene (CB/HDPE) composites were carried out. Change of resistivity ρ is associated with the dynamic modulus before the positive temperature coefficient/negative temperature coefficient (PTC/NTC) transition temperature. When the temperature approaches the melting point of HDPE, ρ increases rapidly with a decreasing modulus, corresponding to PTC transition. The resistivity‐dynamic viscoelasticity relationship in the PTC region can be divided into two parts in which the changes of ρ with storage modulus G′ and loss modulus G″ can be described by the scaling laws given by the critical storage modulus and loss modulus Gc and Gc; adjustable parameters ρ′1c, ρ′2c, ρ″1c and ρ″2c; and nonlinear exponents n and m, respectively. The accordance between the experimental data and the scaling functions of the dimensionless quantities (G′/Gc ? 1) and (G″/Gc ? 1) in the PTC transition region suggests that the ρ jump may be the result of a modulus‐induced percolation. Gc and Gc increase, but the four scaling resistivitis, ρ′1c, ρ′2c, ρ″1c, and ρ″2c, decrease with increasing CB concentration, implying that the microstructure change of the composites is the determinant factor for the PTC behavior and the resistivity‐dynamic modulus relationship. However, ρ′2c and ρ″2c exhibit no scaling dependence. It is suggested that a threshold concentration exists for the modulus of the composites on the basis of examining the plot of both Gc and Gc against CB concentration. The scaling laws G′ ~ Φx and G″ ~ Φy hold for the concentration dependence of the critical modulus when Φ > Φc and the estimated values of x and y are 1.10 ± 0.10 and 0.89 ± 0.29, respectively. The resistivity‐dynamic modulus can shift to form a master curve. The horizontal factors aG and aG and the vertical factors a′ and a″ are relevant to the concentration dependence of the dynamic modulus or PTC behavior. It is believed that the former would be involved in changing the mechanical microstructure formed by the complicated interaction of CB particle and polymer segments, and the latter would be involved in the overall changes of conducting a network during the PTC transition region. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 983–992, 2003  相似文献   

2.
    
The resistivity relaxation behavior under applied voltages in a high‐density polyethylene/graphite nanosheet composite was investigated. The influence of applied voltages on the resistivity relaxation was measured by the collection of the electric current passing through the sample and the increasing temperature of the sample. With increments in the voltage, three distinguishable relaxation curves corresponding to different dominating mechanisms were observed. The sawed curve, corresponding to the application of a high voltage, could be attributed to the reorganization of conductive particles induced by the electric field and the destruction of the conductive network due to the thermal expansion of the high‐density polyethylene matrix. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 860–863, 2007  相似文献   

3.
    
The composite of linear low density polyethylene (LLDPE) with carbon black (CB) and inorganic flame retardant (aluminum hydroxide, Al(OH)3) was prepared by melt-blending method. The effect of cross-linking on the stability of positive temperature coefficient (PTC) of composite and the elimination of negative temperature coefficient (NTC) of composite were investigated. LLDPE was chemically cross-linking with different contents of initiator (dicumyl peroxide, DCP). The cross-linking effects of composite were analyzed by gel content analysis, differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). By the effect of DCP, not only the composite appeared a high PTC intensity, but also the NTC effect of composite was eliminated. In this investigation, the optimum PTC intensity of composite reached 5.87 orders of magnitude for the composition of LLD0.l0C33.7A28, and the PTC transitional temperature of composite decreased with increasing of DCP content. In addition, the good reproducibility of composites was proved by thermal cycling, and successfully passed the test of over-voltage resistance.  相似文献   

4.
    
A series of novel branched polythiophene derivatives bearing different densities of vinylene‐bridges as linking chains were synthesized by a general synthetic strategy. The organic field‐effect transistors, which were fabricated by spin‐coating the polymer solutions onto octadecyltrichlorosilane‐modified SiO2/Si substrates with top‐contact configuration, afforded a high mobility of 8.0 × 10?3 cm2 V?1 s?1 with an on/off ratio greater than 104 and a threshold voltage of about ?3 V in saturation regime. The devices based on these polymers possessed better performance than those of polymers without conjugated bridges and polymers with longer conjugated bridges. These results demonstrated that the combination of conjugated polythiophene backbones and vinylene‐bridges would improve the carrier mobility. As an emerging class of conjugated materials, polymers with vinylene‐bridges as linking chains would open up new opportunities in organic electronics, and their applications in organic electronics are promising. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1381–1392, 2009  相似文献   

5.
Argon plasma-pretreated high-density polyethylene (PHDPE) was blended with the conductive nano carbon black (CB) and inorganic flame retardant (magnesium hydroxide, Mg(OH)2) was added. Influences of the CB content, plasma treatment time, plasma treatment power, and dosage of 60Co γ-ray radiation on positive temperature coefficient (PTC) behaviors of composite were studied. In addition, the over-voltage resistance behavior of the composites was also investigated. The free radical of PHDPE was measured by 1,1-diphenyl-2-picryhydrazyl (DPPH) method. The gel contents of composite were measured by solvent extraction method. The results showed that the room-temperature volume resistivity and PTC effect of composite were improved significantly with plasma treatment. The PHDPE composite with 60Co γ-ray radiation eliminated the negative temperature coefficient (NTC) effect in the composites effectively, and the PTC intensity of composite was increased. With increasing of radiation dosage from 20 Mrads to 80 Mrads, the gel content of composites increased up to 83.84% and the response temperature of composites shifted to low temperature (127.5 °C to 114.8 °C). In this work, the composites also successfully passed the over-voltage resistance test, and possessed good reproducibility.  相似文献   

6.
    
A simple and fast way to measure proton self‐diffusion coefficients of small penetrant molecules in semicrystalline polymers is introduced. The approach takes advantage of the strong static gradient of a mobile single‐sided NMR sensor and it is demonstrated on PE samples with varying degrees of crystallinity fully saturated in either toluene or n‐hexane. The self‐diffusion coefficients were measured using the gradient stimulated echo sequence appended with a CPMG. It is also shown for the first time, with demonstration on PE plates several millimeter thick with different aging histories, that one‐dimensional profiles of self‐diffusion coefficients as a function of depth can be easily obtained.  相似文献   

7.
    
Get a whiff of this : Human olfactory receptor (hOR)‐conjugated polypyrrole (PPy) nanotubes were integrated into the field‐effect transistor (FET) sensor platform for the fabrication of high‐performance bioelectronic noses (see picture, S=source, D=drain). The device can translate and amplify hOR–odorant interaction into a detectable signal, and it showed highly sensitive and specific responses toward a target odorant.

  相似文献   


8.
    
Polymers using new electron‐deficient units, 2‐pyriminecarbonitrile and 2‐fluoropyrimidine, were synthesized and utilized for the photovoltaics. Donor‐acceptor (D‐A) types of conjugated polymers ( PBDTCN, PBDTTCN, PBDTF, and PBDTTF ) containing 4,8‐bis(2‐octyldodecyloxy)benzo[1,2‐b;3,4‐b′]dithiophene (BDT) or 4,8‐bis(5‐(2‐octyldodecyloxy)thiophen‐2‐yl)benzo[1,2‐b:4,5‐b′]dithiophene (BDTT) as electron rich unit and 2‐pyriminecarbonitrile or 2‐fluoropyrimidine as electron deficient unit were synthesized. We designed pyrimidine derivatives in which strong electron‐withdrawing group (C?N or fluorine) was introduced to the C2 position for the generation of strong electron‐deficient property. By the combination with the electron‐rich unit, the pyrimidines will provide low band gap polymers with low highest occupied molecular orbital (HOMO) energy levels for higher open‐circuit voltages (VOC). For the syntheses of the polymers, the electron‐rich and the electron‐deficient units were combined by Stille coupling reaction with Pd(0)‐catalyst. Absorption spectra of the thin films of PBDTTCN and PBDTTF with BDTT unit show shift to a longer wavelength region than PBDTCN and PBDTF with BDT unit. Four synthesized polymers provided low electrochemical bandgaps of 1.56 to 1.96 eV and deep HOMO energy levels between ?5.67 and ?5.14 eV. © 2015 The Authors. Journal of Polymer Science Part A: Polymer Chemistry Published by Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 771–784  相似文献   

9.
    
Summary: An all‐polymer field‐effect transistor (FET) fabricated using an inkjet printing technique is presented in this paper. Poly(3,4‐ethylenedioxythiophene) works as the source/drain/gate electrode material because of its good conductivity. Polypyrrole acts as the semiconducting layer. Poly(vinyl pyrrolidone) K60, an insulating polymer with a dielectric constant of 60, operates as the dielectric layer. All the polymers are diluted with deionized water, and can be printed with a piezoelectric inkjet printing system. The device functions at a depletion mode with low operation voltage. It has a field‐effect mobility of 0.1 cm2 · V−1 · s−1, an on/off ratio of 2.9 × 103, and a subthreshold slope of 2.81 V · decade−1.

Schematic of the all‐polymer FET synthesized here.  相似文献   


10.
    
Poly(o‐aminobenzyl alcohol) (POABA) was grafted with poly(ethylene oxide)s (PEOs) through the reaction of tosylated PEO with both the hydroxide and amine moieties of reduced POABA. Reduced POABA was prepared through the acid‐mediated polymerization of o‐aminobenzyl alcohol, followed by neutralization with an aqueous ammonium hydroxide solution and reduction with hydrazine. The grafted copolymers were very soluble in common polar solvents, such as chloroform, tetrahydrofuran, and dimethylformamide, and the copolymers with longer PEO side chains (number‐average molecular weight > 164) were even water‐soluble. The conductivities of the doped grafted copolymers decreased with increasing PEO side‐chain length because of the nonconducting PEO and its torsional effect on the POABA backbone. The conductivity of highly water‐soluble POABA‐g‐PEO‐350 was 0.689 × 10?3 S/cm, that is, in the semiconducting range. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4756–4764, 2004  相似文献   

11.
    
We report the synthesis and characterization of a polysaccharide crosslinker of tetraaniline grafting oxidized sodium alginate with large aldehyde and carboxylic groups. We demonstrate that this copolymer has the following properties: it is water soluble under any pH, biodegradable, electroactive, and noncytotoxic; it can self-assemble into nanoparticles with large active functional groups on the outer surface; it can crosslink materials with amino and aminoderivative groups like gelatin to form hydrogels, and thus the electroactivity is readily introduced to the materials. This copolymer has potential applications in biomedical fields such as tissue engineering, drug delivery, and nerve probes where electroactivity is required.  相似文献   

12.
    
The syntheses and characterization of poly((2,6‐(4,4‐bis(4‐((2‐ethylhexyl)oxy)phenyl)‐4H‐cyclopenta[def]phenanthrene))‐co‐(2,6‐(4,4‐bis(4‐(((9‐carbazolyl)hexyl)oxy)phenyl))‐4H‐cyclopenta[def]phenanthrene)) (BCzPh‐PCPPs) and poly((2,6‐(4,4‐bis(4‐((2‐ethylhexyl)oxy)phenyl)‐4H‐cyclopenta[def]phenanthrene))‐co‐(2,6‐(4‐(4‐(((9‐carbazolyl)hexyl)oxy)phenyl)‐4‐(4‐((2‐ethylhexyl)oxy)phenyl)‐4H‐cyclopenta[def]phenanthrene))) (CzPh‐PCPPs), with carbazole unit as pendants, are presented. The carbazole moiety, which can improve the hole injection ability, was introduced as a pendant on the PCPP backbone. The devices of the polymers with the configurations of ITO/PEDOT:PSS/polymers/Ca/Al generate EL emission with maximum peaks at 400–450 nm, CIE coordinates of (x = 0.11–0.29, y = 0.11–0.33), low turn‐on voltages of 4–6 V, maximum brightness of 60–810 cd/m2, and luminescence efficiencies of 0.04–0.22 cd/A. The PL spectra of CzPh‐PCPPs films did not show any peak at around 550 nm, which corresponds to keto defect or aggregate/excimer formation, even after annealing for 30 h at 150 °C in air. Out of the series, CzPh‐PCPP1 (PCPP derivative with 10% of carbazole moiety as pendant) shows blue emission with the maximum brightness of 810 cd/m2 at 9 V, and the highest luminescence efficiency of 0.22 cd/A at 395 mA/cm2. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1327–1342, 2009  相似文献   

13.
    
A series of fluorene–thiophene‐based semiconducting materials, poly(9,9′‐dioctylfluorene‐alt‐α,α′‐bisthieno[3,2‐b]thiophene) (F8TT2), poly(9,9′‐di(3,6‐dioxaheptyl)fluorene‐alt‐thieno[3,2‐b]thiophene) (BDOHF8TT), poly(9,9′‐di(3,6‐dioxaheptyl)fluorene‐alt‐bithiophene) (BDOHF8T2), and poly(9,9′‐dioctylfluorene‐co‐bithiophene‐co‐[4‐(2‐ethylhexyloxyl)phenyl]diphenylamine) (F8T2TPA), was synthesized through a palladium‐catalyzed Suzuki coupling reaction. F8TT2, BDOHF8TT, BDOHF8T2, and F8T2TPA films exhibited photoluminescence maxima at 523, 550, 522, and 559 nm, respectively. Solution‐processed field‐effect transistors (FETs) fabricated with all the copolymers except F8T2TPA showed p‐type organic FET characteristics. Studies of the differential scanning calorimetry scans and FETs of the polymers revealed that more crystalline polymers gave better FET device performance. The greater planarity and rigidity of thieno[3,2‐b]thiophene in comparison with bithiophene resulted in higher crystallinity of the polymer backbone, which led to improved FET performance. On the other hand, the random incorporation of the triphenylamine moiety into F8T2TPA caused the polymer chains to lose crystallinity, resulting in an absence of FET characteristics. With this study, we could assess the liquid‐crystallinity dependence of the field‐effect carrier mobility on organic FETs based on liquid‐crystalline copolymers. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4709–4721, 2006  相似文献   

14.
    
To establish the correlation between the thermoelectric properties of conducting polymers and their doping levels, we have utilized the potential-step chronocoulometry for the quantitative estimation of the doping levels. In this paper, three types of poly(3-hexylthiophene)s synthesized by different polymerization methods were investigated. The electrical conductivities and the Seebeck coefficients of poly(3-hexylthiophene)s with various doping levels were measured and plotted against the doping level. It was found that the electrical conductivity linearly increased with increasing the doping level in the range of 1–10%, and then saturated. On the other hand, the relationship between the Seebeck coefficient and the doping level showed a good linearity in all the polymers.  相似文献   

15.
    
This article describes the structure and electrical performance of positive‐temperature‐coefficient/negative‐temperature‐coefficient (PTC/NTC) effects of the following three‐component blends: poly(4‐methyl pentene‐1)/ultra‐high molecular weight polyethylene/carbon black (TPX/UHMWPE/CB), poly(4‐methyl pentene‐1)/crosslinked‐ultra‐high molecular weight polyethylene/carbon black (TPX/XL‐UHMWPE/CB), and γ‐irradiated, compression‐molded plaques of these blends. CB particles are preferentially attracted to the UHMWPE and XL‐UHMWPE particles, which constitute the dispersed phase within the TPX matrix, but practically cannot or can only very slightly penetrate them because of their extremely high viscosity. Thus, CB particles initially form conductive networks on the UHMWPE phase; this is followed by distribution in the TPX matrix, electrically connecting the CB‐covered UHMWPE particles. This unusual CB distribution results in a reduced percolation threshold of all blends. A double‐PTC effect is exhibited by the XL‐UHMWPE‐containing samples. Irradiation of compression‐molded plaques improves their thermoelectric behavior by amplifying the PTC effect and reducing the NTC effect. A schematic model of the double‐PTC effect is suggested, describing the morphological changes of 70TPX/30XL‐UHMWPE/CB blends at different stages of heating with respect to their thermoelectric behavior. Irradiation of TPX/UHMWPE/CB plaques converts these systems into high‐intensity PTC materials free of the NTC effect. © 2001 John Wiley & Sons, Inc. J Polym Sci B Part B: Polym Phys 39: 1415–1428, 2001  相似文献   

16.
The time dependence of dc conductivity of conducting polyaniline films was measured in relation to temperature and relative humidity of the environment. Optical and structural properties of the samples were checked using Fourier transform infrared (FTIR) spectroscopy.  相似文献   

17.
    
Carbon black nanoparticle grafted with poly(N‐isopropylacrylamide) (CB‐g‐PNIPAAm) was synthesized by surface‐initiated atom transfer radical polymerization (SI‐ATRP). The temperature‐responsive behavior of CB‐g‐PNIPAAm was proved by temperature‐variable 1H NMR. A temperature‐dependent conductive composite was prepared by blending CB‐g‐PNIPAAm with epoxy resin. The relationship between temperature and resistivity of the composite was studied: the composite exhibited a negative temperature coefficient (NTC) phenomenon. Possible mechanism for the NTC phenomenon was suggested. The results showed that resultant composites can be used in intelligent temperature‐switching. © 2008 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 1529–1535, 2008  相似文献   

18.
    
Poly(3‐hexylthiophene) (P3HT) is a polymer widely used in organic photovoltaic devices. Discrepancies in information exist in the literature about its morphological structure in solution and in the solid state. This work is a theoretical study, in which the structure of P3HT in the solid state is deduced from its structure in solution and comparisons with optical absorption data. The results indicate that P3HT is not planar, either in solution or in the solid state. However, the effective conjugation length in the solid state is similar to that of a planar chain. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013 , 51, 1350–1354  相似文献   

19.
    
Stimuli‐responsive hydrogels are continuing to increase in demand in biomedical applications. Occluding a blood vessel is one possible application which is ideal for a hydrogel because of their ability to expand in a fluid environment. However, typically stimuli‐responsive hydrogels focus on bending instead of radial uniform expansion, which is required for an occlusion application. This article focuses on using an interdigitated electrode device to stimulate an electro‐responsive hydrogel in order to demonstrate a uniform swelling/deswelling of the hydrogel. A Pluronic‐bismethacrylate (PF127‐BMA) hydrogel modified with hydrolyzed methacrylic acid, in order to make it electrically responsive, is used in this article. An interdigitated electrode device was manufactured containing Platinum electrodes. The results in this paper show that the electrically biased hydrogels deswelled 230% more than the non‐biased samples on average. The hydrogels deswelled uniformly and showed no visual deformations due to the electrical bias. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013 , 51, 1523–1528  相似文献   

20.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号