Academic literature on the topic 'Electrically conductive polymer composites'

Electrically conductive polymer composites are in high demand for modern technologies, however, the intrinsic brittleness of conducting conjugated polymers and the moderate electrical conductivity of engineering polymer/carbon composites have highly constrained their applications. In this work, super high electrical conductive polymer composites were produced by a novel hot embossing design. The polydimethylsiloxane (PDMS) composites containing short carbon fiber (SCF) exhibited an electrical percolation threshold at 0.45 wt % and reached a saturated electrical conductivity of 49 S/m at 8 wt % of SCF. When reducing the sample thickness from 1.0 to 0.1 mm by the hot embossing process, a compression-induced percolation threshold occurred at 0.3 wt %, while the electrical conductivity was further enhanced to 378 S/m at 8 wt % SCF. Furthermore, the addition of a second nanofiller of 1 wt %, such as carbon nanotube or conducting carbon black, further increased the electrical conductivity of the PDMS/SCF (8 wt %) composites to 909 S/m and 657 S/m, respectively. The synergy of the densified conducting filler network by the mechanical compression and the hierarchical micro-/nano-scale filler approach has realized super high electrically conductive, yet mechanically flexible, polymer composites for modern flexible electronics applications.

AbstractThis work is a review of the literature on the possibilities for electroplating of polymer materials. Methods of metalizing polymers and their composites were presented and discussed. Information from various publications on the electrical properties of polymers and polymer composites was collected and discussed. The most important results on the electroplating of conductive polymers and conductive composites were presented and compared. This work especially focuses on the electrical conductivity of polymer materials. The main focus was the efficiency of metal electrodeposition. Based on the analyzed publications, it was found that electrically deposited metal layers on conductive polymeric materials show discontinuity, considerable roughness, and different layer thickness depending on the distance from the contact electrode. The use of metal nanoparticles (AgNWs) or nickel nanoparticles (NiNPs) as a filler enables effective metallization of the polymer composite. Due to the high aspect ratio, it is possible to lower the percolation threshold with a low filler content in the polymer matrix. The presented review reveals many of the problems associated with the effectiveness of the electroplating methods. It indicates the need and direction for further research and development in the field of electroplating of polymer materials and modification of their electrical properties.

Сomposite materials are widely used in various industrial sectors, for example, in the aviation, marine and automotive industries, civil engineering and others. Methods based on measuring the electrical conductivity of a composite material have been actively developed to detect internal damage in polymer composite materials, such as matrix cracking, delamination, and other types of defects, which make it possible to monitor a composite’s state during its entire service life. Polymers are often used as matrices in composite materials. However, almost always pure polymers are dielectrics. The addition of nanofillers, such as graphene and its derivatives, has been successfully used to create conductive composites based on insulating polymers. The final properties of nanomodified composites can be influenced by many factors, including the type and intrinsic properties of nanoscale objects, their dispersion in the polymer matrix, and interphase interactions. The work deals with modeling of effective electric conductive properties of the representative volume elements of nanoscale composites based on a polymer matrix with graphene oxide particles distributed in it. In particular, methods for evaluating effective, electrically conductive properties have been studied, finite element modelling of representative volumes of polymer matrices with graphene oxide particles have been performed, and the influence of the tunneling effect and the orientation of inclusions on the conductive properties of materials have been investigated. The possibility of using models of resistive strain gauges operating on the principle of the tunneling effect is studied. Based on the finite-element modeling and graph theory tools, we created approaches for estimating changes in the conductive properties of the representative volume elements of a nanomodified matrix subjected to mechanical loading.

Tailoring the properties of natural polymers such as electrical conductivity is vital to widen the range of future applications. In this article, the potential of electrically conducting multi-wall carbon nanotube (MWCNT)/polylactic acid (PLA) composites produced by industrially viable melt mixing is assessed simultaneously to MWCNT influence on the composite’s mechanical strength and polymer crystallinity. Atomic force microscopy observations showed that melt mixing achieved an effective distribution and individualization of unmodified nanotubes within the polymer matrix. However, as a trade-off of the poor tube/matrix adhesion, the tensile strength was lowered. With 10 wt% MWCNT loading, the tensile strength was 26% lower than for neat PLA. Differential scanning calorimetric measurements indicated that polymer crystallization after injection moulding was nearly unaffected by the presence of nanotubes and remained at 15%. The resulting composites became conductive below 5 wt% loading and reached conductivities of 51 S m−1 at 10 wt%, which is comparable with conductivities reported for similar nanocomposites obtained at lab scale.

Novel electrically conductive SWCNT-reinforced composites were studied in this work. Incorporating SWCNT into CB/polymer composites provides lowering the percolation threshold. Adding a small quantity of single-walled carbon nanotubes into CB/polymer composites allows reducing CB content in electrically conductive composites and improving rheological and processing properties.

Among smart materials, self-healing is one of the most studied properties. A self-healing polymer can repair the cracks that occurred in the structure of the material. Polyketones, which are high-performance thermoplastic polymers, are a suitable material for a self-healing mechanism: a furanic pendant moiety can be introduced into the backbone and used as a diene for a temperature reversible Diels-Alder reaction with bismaleimide. The Diels-Alder adduct is formed at around 50 °C and broken at about 120 °C, giving an intrinsic, stimuli-responsive self-healing material triggered by temperature variations. Also, reduced graphene oxide (rGO) is added to the polymer matrix (1.6–7 wt%), giving a reversible OFF-ON electrically conductive polymer network. Remarkably, the electrical conductivity is activated when reaching temperatures higher than 100 °C, thus suggesting applications as electronic switches based on self-healing soft devices.

A method of synthesizing the FLG/CNF nanopaper on hydrophilic polycarbonate membrane was investigated. The synergistic effect of few-layer graphene (FLG) and carbon nanofiber (CNF) on the electrical conductivity of shape-memory polymer (SMP) composites reinforced by the FLG/CNF nanopaper was explored. The conductive FLG/CNF nanopaper facilitates the actuation in SMP composite induced by electrically resistive heating. The heat conduction in a nanopaper depends greatly on FLG/CNF network formation. The morphology and structure of the FLG/CNF nanopaper are characterized with scanning electronic microscopy (SEM). The flat surface and tunable network structures observed from the microscopic images indicate that the FLG/CNF nanopaper could have highly conductive property. Detailed structural characterization indicates that the three-dimensional networks of nanopaper, result in both the reduction of thermal contact resistance and the enhancement of conductive property along the thickness.

Electrically conductive nanocomposites polymer of poly(vinyl alcohol)/PVA, glutaraldehyde (GA) and multiwalled carbon nanotubes (MWCNT) has been successfully synthesized. The polymer nanocomposites were prepared by mixing PVA, GA (crosslinker), and MWCNT dispersion with an aid of ultrasonic homogenizer at 50 °C. The content of MWCNT, in particular, was varied in order to determine the effect of MWCNT on electrical conductivity of polymer composites. The polymer mixture was casted into a disc to obtain thin film. The electrical conductivity, surface morphology, and mechanical properties of the composites film were investigated by means of four probes method, FTIR spectroscopy, X-ray diffraction, SEM, AFM, and tensile strength measurement, respectively. It was found that the optimum composition of PVA (10%): GA (1%): MWCNT (1%) was 20:20:3 in volume ratio. The addition of MWCNT induced the electrically conductive network on polymer matrix where the electrical conductivity of nanocomposites film significantly increased up to 8.28 x 10-2 S/sq due to reduction of the contact resistance between conductive filler. Additionally, the mechanical strength of nanocomposites polymer were significantly increased as a result of MWCNT addition. Modification of morphological structure of composite film as indicated by FTIR spectra, X-ray diffraction patterns, SEM, and AFM images verified the effective MWCNT filler network in the polymer matrix.

Electrically conductive polymer composites, i.e. polymers filled with conductive fillers, may display a broad range of electrical properties. A rational design of fillers, filler surface chemistry and filler loading can tune the electrical properties of the composites to meet the requirements of specific applications. In this dissertation, two studies were discussed. In the first study, highly conductive composites with electrical conductivity close to that of pure metals were developed as environmentally-friendly alternatives to tin/lead solder in electronic packaging. Conventional conductive composites with silver fillers have an electrical conductivity 1~2 orders of magnitude lower than that of pure, even at filler loadings as high as 80-90 wt.%. It is found that the low conductivity of the polymer composites mainly results from the thin layer of insulating lubricant on commercial silver flakes. In this work, by modifying the functional groups in polymer backbones, the lubricant layer on silver could be chemically reduced in-situ to generate silver nanoparticles. Furthermore, these nanoparticles could sinter to form metallurgical bonds during the curing of the polymer matrix. This resulted in a significant electrical conductivity enhancement up to 10 times, without sacrificing the processability of the composite or adding extraneous steps. This method was also applied to develop highly flexible/stretchable conductors as building block for flexible/stretchable electronics. In the second study, a moderately conductive carbon/polymer composite was developed for use in sensors to monitor the thermal aging of insulation components in nuclear power plants. During thermal aging, the polymer matrix of this composite shrank while the carbon fillers remained intact, leading to a slight increase in filler loading and a substantial decrease in the resistivity of the sensors. The resistivity change was used to correlate with the aging time and to predict the need for maintenance of the insulation component according to Arrhenius’ equation. This aging sensor realized real-time, non-destructive monitoring capability for the aging of the target insulation component for the first time.

Thesis (M. S.)--Materials Science and Engineering, Georgia Institute of Technology, 2009.
Committee Chair: Rosario Gerhardt; Committee Member: Gleb Yushin; Committee Member: Hamid Garmestani. Part of the SMARTech Electronic Thesis and Dissertation Collection.

O objetivo deste estudo foi o desenvolvimento de compósitos poliméricos flexíveis e altamente condutores elétricos preparados por moldagem por compressão e por fabricação de filamentos fundidos (FFF) para possíveis aplicações como materiais piezoresistivos ou piezoelétricos para sensores de compressão. Compósitos baseados em misturas de poli(fluoreto de vinilideno)/poliuretano termoplástico (PVDF/TPU) como matriz e contendo várias frações de negro de fumo-polipirrol (CB-PPy) como aditivo condutor foram preparados. Diversas técnicas de caracterização foram realizadas para avaliar as propriedades mecânicas, térmicas, químicas e elétricas, morfologia e printabilidade dos materiais investigados. Primeiro, blendas de PVDF/TPU com diferentes composições foram produzidas por mistura por fusão seguida de moldagem por compressão. Os resultados mostraram que a flexibilidade desejada para os materiais foi melhorada com a adição de TPU aos compósitos de PVDF. As imagens SEM evidenciaram a obtenção de uma blenda co-contínua com 50/50 vol% de PVDF/TPU. As blendas compostas de PVDF/TPU 38/62 vol% e a blenda co-contínua de PVDF/TPU 50/50 vol% foram selecionadas como matrizes para a preparação de compósitos moldados por compressão e impressos em 3D a fim de alcançar uma ótima combinação entre condutividade, propriedades mecânicas e printabilidade. Várias quantidades de negro de fumo-polipirrol, de 0 a 15%, foram adicionadas às blendas selecionadas para aumentar a condutividade elétrica dos compósitos e possivelmente atuar como agente nucleante para a fase cristalina do PVDF a fim de aumentar sua resposta piezoelétrica. A adição de CB-PPy aumentou a condutividade elétrica de todos os compósitos. No entanto, a condutividade elétrica dos compósitos baseados em blendas co-contínuas PVDF/TPU 50/50 vol% foi maior do que as encontradas para os compósitos de PVDF/TPU 38/62 vol% com mesma concentração de aditivo. De fato, o limiar de percolação elétrico dos compósitos com blenda co-contínua foi de 2%, enquanto o limiar de percolação elétrico dos compósitos compostos da blenda não contínua foi de 5%. Com relação às propriedades mecânicas, a incorporação do aditivo condutor nas blendas resultou em materiais mais rígidos com maior módulo de elasticidade, menor alongamento na ruptura e maior módulo de armazenamento. O módulo de armazenamento (G') e a viscosidade complexa (η*) dos compósitos aumentaram com a adição de CB-PPy. O limiar de percolação reológico foi de 3% para PVDF/TPU/CB-PPy 38/62 vol% e 1% para PVDF/TPU/CB-PPy 50/50 vol%, indicando que uma quantidade maior de carga poderia comprometer a processabilidade dos compósitos. A adição de CB-PPy também resultou na redução dos valores de Tg e Tm dos compósitos devido à redução da mobilidade das cadeias poliméricas. Com base na condutividade elétrica e no comportamento mecânico dos compósitos, três composições diferentes foram selecionadas para a extrusão de filamentos para serem posteriormente utilizados no processo de impressão 3D. No geral, as peças impressas em 3D apresentaram propriedades mecânicas e elétricas inferiores devido à presença de vazios, defeitos e camadas sobrepostas que podem dificultar o fluxo de elétrons. Os valores de condutividade elétrica dos compósitos impressos em 3D de PVDF/TPU/CB-PPy 38/62 vol% contendo 5% e 6% de CB-PPy são de uma a sete ordens de grandeza menores do que os encontrados para os compósitos com a mesma composição moldados por compressão. Mesmo que o valor da condutividade elétrica para o compósito PVDF/TPU 38/62 vol% com 6% de CB-PPy moldado por compressão foi de 1,94x10-1 S•m-1, o compósito impresso em 3D com a mesma composição mostrou um valor muito baixo de condutividade elétrica de 6,01x10-8 S•m-1. Por outro lado, o compósito co-contínuo de PVDF/TPU 50/50 vol% com 10% de aditivo impresso em 3D apresentou um alto valor de condutividade elétrica de 4,14×100 S•m-1 mesmo após o processo de impressão. Além disso, as respostas piezoresistivas dos compósitos foram investigadas. Para os compósitos PVDF/TPU/CB-PPy 38/62 vol%, as amostras moldadas por compressão e impressas em 3D com 5% e 6% de CB-PPy exibiram boa resposta piezoresistiva. No entanto, apenas os compósitos com 6% de aditivo apresentaram valores elevados de sensibilidade e gauge factor, atuação em ampla faixa de pressão e respostas piezoresistivas reprodutíveis durante a aplicação de 100 ciclos de compressão/descompressão para ambos os métodos de fabricação. Por outro lado, para os compósitos co-contínuos de PVDF/TPU/CB-PPy apenas a amostra moldada por compressão com 5% de CB-PPy apresentou respostas piezorresistivas boas e reprodutíveis. A cristalinidade e o teor de fase β do PVDF foram investigados para os compósitos. Embora o grau de cristalinidade das amostras tenha diminuído com a adição de CB-PPy, a porcentagem de fase β no PVDF aumentou. O coeficiente piezoelétrico d33 das amostras aumentou com a porcentagem de fase β. A adição de 6% ou mais de CB-PPy foi necessária para aumentar significativamente o coeficiente piezoelétrico (d33) dos compósitos. O conteúdo de fase β e as respostas piezoelétricas do PVDF foram menores para as amostras preparadas por FFF. Por fim, como pesquisa colateral, a eficiência de blindagem contra interferência eletromagnética (EMI-SE) foi medida para todos os compósitos. Compósitos com maior condutividade elétrica apresentaram melhor blindagem da radiação eletromagnética. Além disso, os compósitos baseados na blenda co-contínua apresentaram maior eficiência de blindagem contra EMI do que os compósitos de PVDF/TPU 38/62 vol%. O principal mecanismo de blindagem foi a absorção para todos os compósitos. As amostras preparadas por FFF apresentaram respostas de EMI-SE menores quando comparadas às amostras moldadas por compressão.
The aim of this study was the development of flexible and highly electrically conductive polymer composites via compression molding and fused filament fabrication for possible applications as piezoresistive or piezoelectric materials for pressure sensors. Composites based on blends of poly(vinylidene fluoride)/thermoplastic polyurethane (PVDF/TPU) as matrix and containing various fractions of carbon black-polypyrrole (CB-PPy) as conductive filler were prepared. Several characterization techniques were performed in order to evaluate the mechanical, thermal, chemical and electrical properties, morphology and printability of the investigated materials. First, PVDF/TPU blends with different compositions were prepared by melt compounding followed by compression molding. The results showed that the flexibility aimed for the final materials was improved with the addition of TPU to PVDF composites. SEM images evidenced the achievement of a co-continuous blend comprising 50/50 vol% of PVDF/TPU. The blends composed of PVDF/TPU 38/62 vol% and the co-continuous blend of PVDF/TPU 50/50 vol% were selected as matrices for the preparation of compression molded and 3D printed composites in order to achieve an optimal compromise between electrical conductivity, mechanical properties and printability. Various amounts of carbon black-polypyrrole, from 0 up to 15%, were added to the selected blends in order to rise the electrical conductivity of the composites and to possible act as nucleating filler for the β crystalline phase of PVDF in order to increase its piezoelectric response. The addition of CB-PPy increased the electrical conductivity of all composites. However, the electrical conductivity of composites based on PVDF/TPU 50/50 vol% co-continuous blends was higher than those found for PVDF/TPU 38/62 vol% composites at the same filler content. Indeed, the electrical percolation threshold of the conductive co-continuous composite blends was 2%, while the electrical percolation threshold of the composites with the nonco-continuous composite blends was 5%. With respect to the mechanical properties, the incorporation of the filler into the blends leaded to more rigid materials with higher elastic modulus, lower elongation at break and higher storage modulus. The storage modulus (G’) and complex viscosity (η*) of the composites increased with the addition of CB-PPy. The rheological percolation threshold was found to be 3% for PVDF/TPU/CB-PPy 38/62 vol% and 1% for PVDF/TPU/CB-PPy 50/50 vol%, indicating that higher amount of filler could compromise the processability of the composites. The addition of CB-PPy also resulted in a reduction on the Tg and Tm values of the composites due to the reduction of the mobility of the polymeric chains. Based on the electrical conductivity and mechanical behavior of the composites, three different compositions were selected for the extrusion of filaments to be used in a 3D printing process. Overall, the 3D printed parts presented lower mechanical and electrical properties because of the presence of voids, defects and overlapping layers that can hinder the flow of electrons. The electrical conductivity values of PVDF/TPU/CB-PPy 38/62 vol% composites containing 5% and 6 wt% of CB-PPy 3D printed samples are one to seven orders of magnitude lower than those found for compression molded composites with the same composition. Even if the electrical conductivity value for PVDF/TPU 38/62 vol% compression molded composite with 6% of CB-PPy was as high as 1.94x10-1 S•m-1, the 3D printed composite with same composition showed a very low electrical conductivity of 6.01x10-8 S•m-1. On the other hand, the 3D printed co-continuous composite PVDF/TPU 50/50 vol% with 10% of filler displayed a high value of electrical conductivity of 4.14×100 S•m-1 even after the printing process. Moreover, the piezoresistive responses of the composites were investigated. For PVDF/TPU/CB-PPy 38/62 vol% composites, the compression molded and 3D printed samples with 5% and 6% of CB-PPy exhibited good piezoresistive response. However, only the composites with 6% displayed high sensitivity and gauge factor values, large pressure range and reproducible piezoresistive responses under 100 cycles for both methods. On the other hand, for PVDF/TPU/CB-PPy co-continuous composites only the compression molded sample with 5% of CB-PPy presented good and reproducible piezoresistive responses. The crystallinity and β phase content of PVDF were investigated for the composites. Althought the degree of crystallinity of the samples decreased with the addition of CB-PPy, the percentage of β phase in PVDF was increased. The piezoelectric coefficient d33 of the samples increased with the percentage of β phase. The addition of 6% or more of CB-PPy was necessary to increase significatively the piezoelectric coefficient (d33) of the composites. The β phase content and piezoelectric responses of PVDF were lower for samples prepared by FFF. Finally, as a collateral research, the electromagnetic interference shielding effectiveness (EMI-SE) were measured for all composites. Composites with higher electrical conductivity showed better shielding of the electromagnetic radiation. In addition, composites based on the co-continuous blend displayed higher EMI shielding efficiency than 38/62 vol% composites. The main mechanism of shielding was absorption for all composites. Specimens prepared by FFF displayed diminished EMI-SE responses when compared to compression molded samples.
Lo scopo di questo studio è lo sviluppo di compositi polimerici flessibili e ad elevata conducibilità elettrica tramite stampaggio a compressione e manifattura additiva (fused filament fabrication) per possibili applicazioni come materiali piezoresistivi o piezoelettrici in sensori di pressione. In particolare, sono stati preparati compositi a base di miscele di poli(vinilidene fluoruro)/poliuretano termoplastico (PVDF/TPU) come matrice e contenenti varie frazioni di nerofumo-polipirrolo (CB-PPy) come riempitivo conduttivo. Sono state utilizzate diverse tecniche di caratterizzazione al fine di valutare le proprietà meccaniche, termiche, chimiche ed elettriche, la morfologia e la stampabilità dei materiali ottenuti. In primo luogo, miscele PVDF/TPU con diverse composizioni sono state preparate mediante mescolatura allo stato fuso seguita da stampaggio a compressione. I risultati hanno mostrato che la flessibilità del PVDF viene notevolemente migliorata dall’aggiunta di TPU. Le immagini SEM hanno evidenziato il raggiungimento di una miscela co-continua per una composizione 50/50% in volume di PVDF/TPU. Le miscele composte da PVDF/TPU 38/62 vol% e la miscela co-continua di PVDF/TPU 50/50 vol% sono state selezionate come matrici per la preparazione di compositi per stampaggio a compressione e manifattura additiva al fine di ottenere un compromesso ottimale tra conducibilità, proprietà meccaniche e stampabilità. Alle miscele selezionate sono state aggiunte varie quantità di nerofumo-polipirrolo, dallo 0 al 15%, per aumentare la conducibilità elettrica dei compositi ed eventualmente fungere da additivo nucleante per la fase β cristallina del PVDF al fine di aumentarne la risposta piezoelettrica. L'aggiunta di CB-PPy ha aumentato la conduttività elettrica di tutti i compositi. Tuttavia, la conduttività elettrica dei compositi basati su miscele co-continue di PVDF/TPU 50/50% in volume era superiore a quella trovata per compositi PVDF/TPU 38/62% in volume con lo stesso contenuto di riempitivo. Infatti, la soglia di percolazione elettrica delle miscele conduttive era del 2%, mentre la soglia di percolazione elettrica dei compositi con miscele composite non continue era del 5%. Per quanto riguarda le proprietà meccaniche, l'incorporazione del riempitivo nelle mescole ha portato a materiali più rigidi con modulo elastico più elevato, allungamento a rottura inferiore e modulo conservativo più elevato. Il modulo conservativo (G') e la viscosità complessa (η*) dei compositi sono aumentate con l'aggiunta di CB-PPy. La soglia di percolazione reologica è risultata essere del 3% per PVDF/TPU/CB-PPy 38/62 vol% e dell'1% per PVDF/TPU/CB-PPy 50/50 vol%, indicando che una maggiore quantità di riempitivo potrebbe compromettere la processabilità dei compositi. L'aggiunta di CB-PPy ha comportato anche una riduzione dei valori di Tg e Tm dei compositi a causa della riduzione della mobilità delle catene polimeriche. Sulla base della conduttività elettrica e del comportamento meccanico dei compositi, sono state selezionate tre diverse composizioni per l'estrusione di filamenti da utilizzare in un processo di stampa 3D. Nel complesso, le parti stampate in 3D presentavano proprietà meccaniche ed elettriche inferiori a causa della presenza di vuoti, difetti e strati sovrapposti che possono ostacolare il flusso di elettroni. I valori di conducibilità elettrica dei compositi PVDF/TPU/CB-PPy 38/62 vol% contenenti il 5% e il 6% di CB-PPy di campioni stampati in 3D sono da uno a sette ordini di grandezza inferiori a quelli trovati per i compositi stampati a compressione con la stessa composizione. Anche se il valore di conducibilità elettrica per il composito stampato a compressione PVDF/TPU 38/62 vol% con il 6% di CB-PPy era pari a 1,94x10-1 S•m-1, il composito stampato in 3D con la stessa composizione ha mostrato un valore molto basso di conducibilità elettrica, pari a 6,01x10-8 S•m-1. D'altra parte, il composito PVDF/TPU 50/50 vol% stampato in 3D con il 10% di riempitivo ha mostrato un elevato valore di conducibilità elettrica, pari a 4,14 × 100 S•m-1, anche dopo il processo di stampa. Inoltre, sono state studiate le risposte piezoresistive dei compositi. Per i compositi PVDF/TPU/CB-PPy 38/62 vol%, i campioni stampati a compressione e stampati in 3D con il 5% e il 6% di CB-PPy hanno mostrato una buona risposta piezoresistiva. Tuttavia, solo i compositi con il 6% hanno mostrato valori di sensibilità e gauge factor elevati, ampio intervallo di pressione e risposte piezoresistive riproducibili in 100 cicli per entrambi i metodi. D'altra parte, per i compositi co-continui PVDF/TPU/CB-PPy solo il campione stampato a compressione con il 5% di CB-PPy ha presentato risposte piezoresistive adeguate e riproducibili. La cristallinità e il contenuto di fase β del PVDF sono stati studiati per i compositi. Sebbene il grado di cristallinità dei campioni diminuisca con l'aggiunta di CB-PPy, la percentuale di fase β in PVDF risulta aumentata. Il coefficiente piezoelettrico d33 dei campioni aumenta anch’esso con la percentuale di fase β. L'aggiunta del 6% o più di CB-PPy è stata necessaria per aumentare significativamente il coefficiente piezoelettrico (d33) dei compositi. Il contenuto di fase β e le risposte piezoelettriche del PVDF sono inferiori per i campioni ottenuti mediante stampa 3D. Infine, come ricerca collaterale, è stata misurata l'efficacia della schermatura contro le interferenze elettromagnetiche (EMI-SE) per tutti i compositi. I compositi con una maggiore conduttività elettrica hanno mostrato una migliore schermatura della radiazione elettromagnetica. Inoltre, i compositi basati sulla miscela co-continua hanno mostrato un'efficienza di schermatura EMI maggiore rispetto ai compositi a 38/62% in volume. Per tutti i compositi, il principale meccanismo di schermatura è l'assorbimento. I campioni preparati mediante manifattura additiva hanno mostrato risposte EMI-SE inferiori rispetto ai campioni stampati a compressione.

The aim of this study was to improve the mechanical and electrical properties of conductive polymer composites. For this purpose, different studies were performed in this dissertation. In order to investigate the effects of the carbon nanotube (CNT) surface treatment on the morphology, electrical and mechanical properties of the composites, poly(ethylene terephthalate) (PET) based conductive polymer composites were prepared by using as-received, purified and modified carbon nanotubes in a twin screw extruder. During the purification of carbon nanotubes, surface properties of carbon nanotubes were altered by purifying them with nitric acid (HNO3), sulfuric acid (H2SO4), ammonium hydroxide (NH4OH) and hydrogen peroxide (H2O2) mixtures. Electron Spectroscopy for Chemical Analysis (ESCA) results indicated the removal of metallic catalyst residues from the structure of carbon nanotubes and increase in the oxygen content of carbon nanotube surface as a result of purification procedure. Surface structure of the purified carbon nanotubes was also modified by treatment with sodium dodecyl sulfate (SDS), poly(ethylene glycol) (PEG) and diglycidyl ether of Bisphenol A (DGEBA). Fourier Transformed Infrared Spectroscopy (FTIR) spectra of the carbon nanotube samples indicated the existence of functional groups on the surfaces of carbon nanotubes after modification. All composites prepared with purified and modified carbon nanotubes had higher electrical resistivities, tensile and impact strength values than those of the composite based on as-received carbon nanotubes, due to the functional groups formed on the surfaces of carbon nanotubes during surface treatment. In order to investigate the effects of alternative composite preparation methods on the electrical and mechanical properties of the composites, in-situ microfiber reinforced conductive polymer composites consisting of high density polyethylene (HDPE), poly(ethylene terephthalate) and carbon nanotubes were prepared in a twin screw extruder followed by hot stretching of PET/CNT phase in HDPE matrix. Composites were produced by using as-received, purified and PEG treated carbon nanotubes. SEM micrographs of the hot stretched composites pointed out the existence of in-situ PET/CNT microfibers dispersed in HDPE matrix up to 1 wt. % carbon nanotube loadings. Electrical conductivity values of the microfibrillar composites were higher than that of the composites prepared without microfiber reinforcement due to the presence of continuous PET/CNT microfibers with high electrical conductivity in the structure. To investigate the potential application of conductive polymer composites, the effects of surfactant usage and carbon nanotube surface modification
on the damage sensing capability of the epoxy/carbon nanotube/glass fiber composite panels during mechanical loadings were studied. Surface modification of the carbon nanotubes was performed by using hexamethylene diamine (HMDA). 4-octylphenol polyethoxylate (nonionic) (Triton X-100) and cetyl pyridinium chloride (cationic) (CPC) were used as surfactants during composite preparation. Electrical resistivity measurements which were performed during the impact, tensile and fatigue tests of the composite panels showed the changes in damage sensing capabilities of the composites. Surface treatment of carbon nanotubes and the use of surfactants decreased the carbon nanotube particle size and improved the dispersion in the composites which increased the damage sensitivity of the panels.

With excellent electrical, thermal and mechanical properties as well as large specific surface area, graphene has been applied in next-generation nano-electronics, gas sensors, transparent electrical conductors, thermally conductive materials, and superior energy capacitors etc. Convenient and productive preparation of graphene is thereby especially important and strongly desired for its manifold applications. Chemically developed functionalized graphene from graphene oxide (GO) has significantly high productivity and low cost, however, toxic chemical reduction agents (e.g. hydrazine hydrate) and raised temperature (400-1100°C) are usually necessary in GO reduction yet not preferred in current technologies. Here, microwaves (MW) are applied to reduce the amount of graphene oxide (GO) at a relatively low temperature (~165°C). Experimental results indicate that resurgence of interconnected graphene-like domains contributes to a low sheet resistance with a high optical transparency after MW reduction, indicating the very high efficiency of MW in GO's reduction. Moreover, graphene is usually recumbent on solid substrates, while vertically aligned graphene architecture on solid substrate is rarely available and less studied. For TIMs, electrodes of ultracapacitors, etc, efficient heat dissipation and electrical conductance in normal direction of solid surfaces is strongly desired. In addition, large-volume heat dissipation requires a joint contribution of a large number of graphene sheets. Graphene sheets must be aligned in a large scale array in order to meet the requirements for TIM application. Here, thermally conductive fuctionalized multilayer graphene sheets (fMGs) are efficiently aligned in a large scale by vacuum filtration method at room temperature, as evidenced by SEM images and polarized Raman spectroscopy. A remarkably strong anisotropy in properties of aligned fMGs is observed. Moreover, VA-fMG TIMs are prepared by constructing a three-dimensional vertically aligned functionalized multilayer graphene architecture between contact Silicon/Silicon surfaces with pure Indium as a metallic medium. Compared with their counterpart from recumbent A-fMGs, VA-fMG TIMs have significantly higher equivalent thermal conductivity and lower contact thermal resistance. Electrical and thermal conductivities of polymer composite are also greatly interested here. Previous researches indicated that filler loading, morphology of fillers, and chemical bonding across filler/polymer interfaces have significant influence on electrical/thermal conductivity of polymer composite. Therefore, the research also pays substantial attention to these issues. First, electrical resistivity of CPCs is highly sensitive on volume or weight ratio (filler loading) of conductive fillers in polymer matrix, especially when filler loading is close to percolation threshold (pc). Thermal oxidation aging usually can cause a significant weight loss of polymer matrix in a CPC system, resulting in a filler loading change which can be exhibited by a prompt alteration in electrical resistivity of CPCs. Here, the phenomena are applied as approach for in-situ monitoring thermal oxidation status of polymeric materials is developed based on an electrical sensors based on conductive polymeric composites (CPCs). The study developed a model for electrical resistivity of sensors from the CPCs as a function of aging time at constant aging temperature, which is in a good agreement with a Boltzmann-Sigmoidal equation. Based on the finding, the sensors show their capability of in-situ in-situ monitor and estimate aging status of polymeric components by a fast and convenient electrical resistance measurement. Second, interfacial issues related to these thermal conductive fillers are systemically studied. On the one hand, the study focuses on relationship between morphology of h-BN particles and thermal conductivity of their epoxy composites. It is found that spherical-agglomeration of h-BN particles can significantly enhance thermal conductivity of epoxy resin, compared with dispersed h-BN plates, by substantially reducing specific interfacial area between h-BN and epoxy resin. On the other hand, surface of high thermal conductive fillers such as SiC particles and MWNTs are successfully functionalized, which makes their surface reactive with bisphenol A diglycidyl ether and able to form chemical bonding between fillers and epoxy resin. By this means, thermal conductivity of polymer composites is found to be significantly enhanced compared with control samples, indicating the interfacial chemical bonding across interface between thermal conductive fillers and polymer matrix can promote heat dissipation in polymeric composites. The finding can benefit a development of high thermal conductive polymer composites by interfacial chemical bonding enhancement to meet the demanding requirements in current fine pitch and Cu/low k technology.

Carbon nanotube (CNT)-polymer composites were prepared by segregated network approach. CNTs were served as conductive fillers in a polymer matrix to synthesize electrically conducting polymer composites. In the segregated network composites, the thermoelectric properties were further improved by replacing Gum Arabic (GA) with electrically conductive stabilizer PEDOT:PSS doped with dimethyl sulfoxide (DMSO). The electrical and thermal conductivities and Seebeck coefficient were measured to determine the thermoelectric property of the polymer composites. The electrical conductivity of the composites with 9.8wt% of CNT was 3191.8 S/m whereas that of 10wt% CNT composite with GA sample was 400 S/m.

The present paper investigates three types of electrically conductive polymers (ECPs), namely polyaniline, polypyrrole and poly(3,4-ethylenedioxythiophene) PEDOT composite with multi-walled carbon nanotubes (CNTs) for supercapacitor applications. Their capacitive performance has been evaluated in both three electrodes half-cell and two electrodes cell setup. The nanocomposite were fabricated by polymerizing pseudocapacitive conductive polymer onto the MWCNT surface through the in-situ chemical polymerization approach. The composites were aimed to be optimized through varying the ECPs to MWCNT ratios. Half-cell electrochemical study was conducted to determine the optimal proportion of MWCNT and ECP in this parametric study. Two electrodes cell electrochemical study unveiled the potential device’s energy storage performance. MWCNT was found to act as the framework for the polymerization of the ECP into a tubular structure. Among the three composites, Ppy/MWCNT composite showed superior supercapacitor characteristics at scan rates of up to 500mV/s.

The growing popularity of Poly lactic acid (PLA) is related to its biocompatibility, good mechanical properties, and its synthesis from renewable resources. PLA can be compounded with electrically conductive fillers (e.g., carbon nanotubes (CNTs)) to form carbon polymer composites (CPC). These fillers provide the conductive functionality by forming percolative paths. Featuring very low weight densities, CPCs have the potential to replace metals in the electronic industry if they exhibit similar electrical conductivities. The current challenges being faced during the mixing of CNTs in a polymer matrix are the formation of aggregates due to the strong van der Waals forces and the breakage of the CNTs during dispersion. In this study, we compare: (1) two fabrication methods to create CPCs (i.e., solution mixing by sonication and extrusion) and (2) effects of various CNT functionalization techniques (i.e., acid and plasma treatments) on the conductivity of the CPCs. First, the composites comprising of 30% PLA by weight in Dichloromethane (DCM) and CNTs in different concentrations (up to 5wt.%) are fabricated by two step sonication method (i.e., dissolving PLA in DCM and then dispersing the CNTs in the polymer solution). Second, CPCs are fabricated using a micro twin screw extruder operating at 180°C. To verify the effects of functionalization of the CNTs on the conductivity of composites, the CNTs are functionalized via three methods: - HNO3 acid functionalization, 3:1 ratio HNO3 + H2SO4 acid (stronger) functionalization and N2 plasma functionalization. CPC fibers are drawn using the solvent-cast printing method. These fibers are then tested for their electrical conductivity using the two probe method. The maximum electrical conductivity is showed by the 5% CNT concentration samples at 3.97 S/m and 25.16 S/m for the CPC fibers obtained via the solution blend and the extrusion methods, respectively. Regarding the functionalized CNTs, conductivity measurements show a negative effect of the CNTs functionalization on the electrical properties of the CPC.

Electromagnetic (EM) waves, such as electronic noise and radio frequency interference can be regarded as an invisible electronic pollution which justifies a very active quest for effective electromagnetic interference (EMI) shielding materials. Highly conductive materials of adequate thickness are the primary solutions to shield against EMI. Equipment cases and basic structure of space aircraft and launch vehicles have traditionally been made of aluminum, steel and other electrically conductive metals. However, in recent years composite materials have been used for electronic equipment manufacturing because of their lightweight, high strength, and ease of fabrication. Despite these benefits, composite materials are not as electrically conductive as traditional metals, especially in terms of electrical grounding purposes and shielding. Therefore, extra effort must be taken to resolve these shortcomings. The present work demonstrates a study on developing hybrid composites based on fiberglass with surface grown carbon nanotubes (CNTs) for EMI applications. The choice of fiberglass is primarily because it naturally possesses poor electrical conductivity, hence growing CNTs over glass fiber surface can significantly improve the conductivity. The fabrics were sputter-coated with a thin layer of SiO2 thermal barrier prior to growing of CNTs. The CNTs were grown on the surface of woven fiberglass fabrics utilizing a relatively low temperature technique. Raw fiberglass fabric, SiO2 coated fabric, and SiO2 coated fabric which was subjected to the identical heat treatment as the samples with CNTs were also prepared. Two-layers composite specimens based on different surface treated fiberglass fabrics were fabricated and their EMI shielding effectiveness (SE) was measured. The EMI SE of the hybrid CNT-fiberglass composites was shown to be 5–10 times of the reference samples. However, the tensile mechanical properties of the composites based on the different above mentioned fibers revealed significant degradation due to the elevated CNT growth temperature and the addition of coating layer and CNTs. To further probe the structure of the hybrid composites and the inter-connectivity of the CNTs from one interface to another, sets of 20-layers composites based on different surface treated fabrics were also fabricated and characterized.

Abstract Carbon fibre reinforced polymers (CFRPs) are more and more used in a wide range of industries, especially in the aerospace industry, but their low electrical conductivity has limited their application. During the past few years, metallization of CFRP has attracted increasing interest. To make the polymer composites electrically conductive, a conductive media must be either embedded into or coated onto the composites. Cold spray is one coating approach to achieve this. In this work, metallic powders were cold sprayed onto the CFRPs used in aircraft by using two different cold spray systems. The coatings as well as the coating/substrate interfaces were characterized and the deposition mechanism onto the CFRP substrate was determined.

The application of polymer-based micro-patterns in the field of flexible micro-electronics has become the focus as to replace rigid and planar silicon based integrated circuits with weak bendability. Polyethylene terephthalate (PET) can be used as a substrate because of its excellent flexible and mechanical properties and polyaniline (PANI) is a typical representative of the electrical conductive polymers applicable for this purpose. PANI excels by a stable and controllable electrical conductivity, high environment stability, and ease fabrication. An improvement of electrical conductivity of PANI can be achieved using different nano-particles, such as carbon nanotubes (CNTs). CNTs since their discovery have attracted attention due to their excellent electrical, thermal, and mechanical properties, and had divergent applications, such as complex nano/micro-electronic devices, energy storage and both chemical and bio sensors. This research was focused on the preparation of micro-patterns based on electrically conductive PANI using shaping mold and cold plasma acting as adhesion promoter for PET substrate. The PANI/CNTs nano-composite was used to enhance an electrical conductivity of prepared micropatterns. The adhesion of prepared micro-patterns was evaluated based on the peel tests measurement. Various microscopic techniques, such as profilometry, scanning electron microscopy and atomic force microscopy (AFM), proved the homogeneous structures of prepared polymer based micro-patterns. Broad dielectric spectroscopy and conductive AFM confirmed electrical behavior of prepared micro-patterns.

To electrically activate the shape recovery in a styrene-based shape-memory polymer (SMP) by coating with conductive carbon nanofiber paper has been demonstrated in this paper. Carbon nanofibers in the form of paper sheet in combination with SMP significantly improve the electrical and thermal conductivity of polymer, leading to the actuation of SMP/nanopaper composite (with 15% volume fraction of carbon nanopaper, dimension of 10.0 cm × 0.5 cm × 0.3 cm) can be carried out by applying 8.4 V voltage, with response time of 140 s. Therefore, electrical conductivity of 6.6 S/cm is obtained. This approach, although demonstrated in styrene-based polymer, is applicable to other type of SMP materials. Furthermore, the morphologies of carbon nanofiber in the form of paper is observed by scanning electron microscopy, and the thermomechanical properties of composites are measured and analyzed by dynamic mechanical analysis.