Co-reporter:Jingjing Wang;Qian Ren;Shengpei Su
Industrial & Engineering Chemistry Research September 18, 2013 Volume 52(Issue 37) pp:13411-13421
Publication Date(Web):Publication Date (Web): August 16, 2013
DOI:10.1021/ie402039y
In this study, poly(lactic acid) (PLA) resins with linear (L-PLA) and branched structure (B-PLA) were selected, and the solid state foaming technology was applied to prepare PLA foams. B-PLA foams exhibited a high expansion ratio of about 40 and cell density of 105–6 cells/cm3, whereas L-PLA foams only had the highest expansion ratio of 29.8 and cell density of 103–6 cells/cm3. When PLA resins were induced crystallization during CO2 saturation, however, the prepared L-PLA foams presented the highest expansion ratio of 37.4 and cell density of 106–7 cells/cm3. The cell structure evolution of PLA foams with the foaming time suggested that the in situ formed crystal domains supplied nucleating sites to enhance cell nucleation and acted as physical cross-linking points to stabilize cell structure. These interesting results demonstrated that the induced crystallization might be more attractive than the chain modification to improve the foaming behavior using solid state foaming technology.
Co-reporter:Chengbiao Ge, Qian Ren, Shiping Wang, Wenge Zheng, Wentao Zhai, Chul B. Park
Chemical Engineering Science 2017 Volume 174(Volume 174) pp:
Publication Date(Web):31 December 2017
DOI:10.1016/j.ces.2017.09.011
•A novel expanded bead foam described as ETPU was molded through a steam-chest molding process.•The ETPU bonded effectively, the corresponding products had a smooth surface, and good tensile and compressive properties.•A bonding mechanism was proposed.The steam-chest molding process can be used to prepare molded bead foams, including expandable polystyrene (EPS), expanded polyethylene (EPE), expanded polypropylene (EPP), and expanded polylactide (EPLA) with complex three-dimensional shapes. A new thermoplastic elastomer bead foam, which is described as expanded thermoplastic polyurethane (ETPU), now exists. Notably, it has an excellent soft touch quality and is ductile. It has also generated widespread interest in both the academic and industrial communities. In this study, three types of ETPU foams with various sample sizes were steam-chest molded. We concentrated on the preparation of the molded ETPU (METPU), which was followed by a mechanical test. Our morphological observations showed that the ETPU bead foams’ interfaces had effectively bonded. A high tensile strength of 1.80 MPa and an elongation at break of 360.1% were reached in the METPU sample with a density of 0.35 g/cm3. A 200-fold cyclic compression measurement verified that the compressed METPU sample could recover more than 95% both in stress and modulus, after 6 days of relaxation. This suggested the presence of excellent interbead bonding in the ETPU bead foams. Based on the differential scanning calorimetry (DSC) results, we proposed that a formation mechanism for interbead bonding during the ETPU steam-molding process existed.Download high-res image (102KB)Download full-size image
Co-reporter:Bin Shen, Yang Li, Wentao Zhai, and Wenge Zheng
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 12) pp:8050
Publication Date(Web):March 14, 2016
DOI:10.1021/acsami.5b11715
The fabrication of low-density and compressible polymer/graphene composite (PGC) foams for adjustable electromagnetic interference (EMI) shielding remains a daunting challenge. Herein, ultralightweight and compressible PGC foams have been developed by simple solution dip-coating of graphene on commercial polyurethane (PU) sponges with highly porous network structure. The resultant PU/graphene (PUG) foams had a density as low as ∼0.027–0.030 g/cm3 and possessed good comprehensive EMI shielding performance together with an absorption-dominant mechanism, possibly due to both conductive dissipation and multiple reflections and scattering of EM waves by the inside 3D conductive graphene network. Moreover, by taking advantage of their remarkable compressibility, the shielding performance of the PUG foams could be simply adjusted through a simple mechanical compression, showing promise for adjustable EMI shielding. We believe that the strategy for fabricating PGC foams through a simple dip-coating method could potentially promote the large-scale production of lightweight foam materials for EMI shielding.Keywords: adjustable EMI shielding; compressible; low-density; multiple reflections; polymer/graphene composite foams
Co-reporter:Bin Shen, Yang Li, Da Yi, Wentao Zhai, Xingchang Wei, Wenge Zheng
Carbon 2016 Volume 102() pp:154-160
Publication Date(Web):June 2016
DOI:10.1016/j.carbon.2016.02.040
As reported, the foaming of layered graphene films into porous graphene foams could improve their performance for absorbents, catalysis and supercapacitors. Herein, to emphasize the impact of porous structure on electromagnetic interference (EMI) shielding, the direct comparison between graphene film (G-film) and corresponding microcellular graphene foam (G-foam) in terms of EMI shielding efficiency has been investigated in a broadband frequency range of 8.2–59.6 GHz, including X-band, Ku-band, K-band, Ka-band, and U-band. Consequently, despite the lower electrical conductivity of the as-prepared G-foam, it exhibited an improved average shielding effectiveness (SE) of ∼26.3 dB over the entire frequency range in comparison with that of G-film (∼20.1 dB). Implication of the results suggested that the foaming of layered graphene films into porous graphene foams could lead to an improvement in EMI shielding, which should be ascribed to the formation of improved internal multiple reflections at the large cell–matrix interfaces owing to the existence of microcellular structure in G-foam. We believe that this research would open up new opportunity for the development of graphene foams in the field of EMI shielding.
Co-reporter:Qian Ren, Jing Wang, Wentao Zhai, and Richard Eungkee Lee
Industrial & Engineering Chemistry Research 2016 Volume 55(Issue 49) pp:
Publication Date(Web):November 15, 2016
DOI:10.1021/acs.iecr.6b03266
A sinterable poly(lactic acid) (PLA) foam is critical to the creation of strong interface bonding for the production of large-size PLA bead foam products. To fabricate such a foam, we blended a polyethylene glycol (PEG) that has a low melting temperature and high CO2 solubility with PLA. Solid-state foaming technology was used to foam the PLA/PEG blends, and CO2 was the blowing agent. The PEG was miscible with the PLA and enhanced the crystallization of PLA at a loading of lower than 10 wt % under a CO2 saturation process. Consequently, the PLA/PEG blends did not foam well because of the matrix’s improved stiffness. The CO2 saturation process induced the PEG’s phase separation because its content was higher than 20 wt %. This weakened the PEG’s plasticization effect on the PLA, but it significantly improved the PLA’s foaming behavior. This was characterized by both the foam expansion ratio, which increased from 4.6 to 11.8–24.1, and the decreased cell size. We discuss the effects of crystallization and the separated PEG phase on cell nucleation and growth in order to explain the possible operational mechanisms. Both the PEG’s self-diffusion behavior and the PLA/PEG’s improved foaming behavior enabled us to fabricate large-size PLA bead foam products.
Co-reporter:Zhuang Zhang, Guangming Chen, Hanfu Wang and Wentao Zhai
Journal of Materials Chemistry A 2015 vol. 3(Issue 8) pp:1649-1654
Publication Date(Web):16 Jan 2015
DOI:10.1039/C4TC02471K
A new strategy, i.e. interfacial adsorption-soft template polymerization, is developed to enhance polymer thermoelectric property. The obtained nanocomposite 3D interconnected architecture consisting of reduced graphene oxide (rGO) nanolayers sandwiched by polypyrrole (PPy) nanowires is directly confirmed by scanning and transmission electron microscopies. Moreover, the nanocomposites reveal significantly enhanced thermoelectric performance. At rGO:PPy ratio of 50 wt%, the nanocomposite power factor reaches ∼476.1 times that of pure PPy nanowires. Our results suggest that a greatly enhanced thermoelectric property for polymer nanocomposites can be achieved by a complex morphology design.
Co-reporter:Yuejuan Chen, Yang Li, Donghua Xu and Wentao Zhai
RSC Advances 2015 vol. 5(Issue 100) pp:82034-82041
Publication Date(Web):11 Sep 2015
DOI:10.1039/C5RA12515D
Stretchable and flexible conductive polymers have aroused great interest recently because of their applications in the fields of novel electronics, such as smart textiles, artificial electronic skin, flexible electronic displays, etc. In this work, stretchable and flexible conductive thermoplastic polyurethane (TPU)/graphene composite foams have been developed by water vapour induced phase separation. The as-prepared TPU/graphene composite foams exhibited a lower modulus, larger elongation at break, and lower hysteresis during a cycle tensile test than a TPU/graphene composite did. It is expected that the improved elasticity of the TPU/graphene composite foams was caused by the deformation of cells, which partially offset the deformation of the TPU matrix. In addition, the cell walls divided the whole composites into many small parts, which could further restrain plastic deformation of hard segment domains under deformation.
Co-reporter:Yang Li, Xueliang Pei, Bin Shen, Wentao Zhai, Lihua Zhang and Wenge Zheng
RSC Advances 2015 vol. 5(Issue 31) pp:24342-24351
Publication Date(Web):27 Feb 2015
DOI:10.1039/C4RA16421K
Herein Kapton-type aromatic polyimide (PI) composite foams with reduced graphene oxide (rGO) content ranging from 1 to 16 wt% have been fabricated via a three-step method: in situ polymerization, nonsolvent induced phase separation and thermal imidization, and used for electromagnetic interference shielding. The resultant PI/16 wt% rGO foam with low density of 0.28 g cm−3 and thickness of 0.8 mm exhibited an effective EMI shielding effectiveness of 17–21 dB in X band (8–12 GHz). Additionally, the thermostability of the foams was also significantly enhanced, for the 5% weight loss temperature it was improved from 508 °C for the pure PI foam to 520 °C for the PI/1 wt% rGO foam, and consequently, to 581 °C for the PI/16 wt% rGO foam. Even with the high rGO content (16 wt%), the composite foam was fairly flexible. Tensile testing revealed that the PI/16 wt% rGO foam possessed a tensile strength of 11.4 MPa and an elongation at break of 9.6%, respectively.
Co-reporter:Pin Jia, Jie Hu, Wentao Zhai, Yongxin Duan, Jianming Zhang, and Changyu Han
Industrial & Engineering Chemistry Research 2015 Volume 54(Issue 9) pp:2476
Publication Date(Web):February 6, 2015
DOI:10.1021/ie504345y
The preparation of poly(l-lactic acid) (PLLA) foam with well-defined cell structure and high heat resistance is critical to broaden its applications. In this study, the stereocomplex crystallites (SC) with higher melting point and heat stability were introduced into PLLA foam by melt blending the PLLA with different amounts of poly(d-lactic acid) (PDLA). The crystal structures of pure PLLA and PLLA/PDLA blends formed during the blending and molding process were compared. It was found that no obvious crystallization was detected in pure PLLA, while SC formed in PLLA/PDLA blends. Crystal structure and morphology evolution of PLLA and PLLA/PDLA during the CO2 saturation and foaming process were investigated by combination of DSC, WAXD, FTIR, and SEM techniques. The results suggested SC had a higher melting peak, higher thermal stability, and smaller crystal domain size in relation to the homocrystal of PLLA, and it did not further develop with the CO2 saturation and the foaming processes, while the CO2 saturation induced the formation of the mesomorphic structure in PLLA and PLLA/PDLA blends. The mesomorphic structure transformed into the more stable α form in the following foaming process. The resultant PLLA/PDLA foam exhibited a significant and concurrent increase in cell density and cell structure uniformity relative to PLLA foam. The heat resistance measurement presented that thus-prepared PLLA/PDLA foams had better heat resistance than PLLA foam, which was attributed to the higher melting point, higher heat stability, and higher cell nucleation ability of SC in PLLA/PDLA foams.
Co-reporter:Bin Shen;Wenge Zheng
Advanced Functional Materials 2014 Volume 24( Issue 28) pp:4542-4548
Publication Date(Web):
DOI:10.1002/adfm.201400079
As the portable device hardware has been increasing at a noticeable rate, ultrathin thermal conducting materials (TCMs) with the combination of high thermal conductivity and excellent electromagnetic interface (EMI) shielding performance, which are used to efficiently dissipate heat and minimize EMI problems generated from electronic components (such as high speed processors), are urgently needed. In this work, graphene oxide (GO) films are fabricated by direct evaporation of GO suspension under mild heating, and ultrathin graphite-like graphene films are produced by graphitizing GO films. Further investigation demonstrates that the resulting graphene film with only ≈8.4 μm in thickness not only possesses excellent EMI shielding effectiveness of ≈20 dB and high in-plane thermal conductivity of ≈1100 W m-1 K-1, but also shows excellent mechanical flexibility and structure integrity during bending, indicating that the graphitization of GO film could be considered as a new alternative way to produce excellent TCMs with efficient EMI shielding.
Co-reporter:Jingjing Wang, Qian Ren, Wenge Zheng, and Wentao Zhai
Industrial & Engineering Chemistry Research 2014 Volume 53(Issue 4) pp:1422-1430
Publication Date(Web):January 8, 2014
DOI:10.1021/ie403041h
High expansion ratio, well-defined cell structure, and an excellent flame retardant characteristic are essential properties for broadening the applications of polymeric foam. In this study, by applying microcellular foaming technology using compressed CO2 as the blowing agent, we are challenged to synthesize the desirable poly(lactic acid) (PLA) foams with phosphorus-containing flame retardant (FR) and starch as the natural charring agent. It was interesting to find that the introduction of 15–25 wt % FR increased the limiting oxygen index (LOI) of PLA foams from 18.2% to 24.8–28.4% and simultaneously increased the foam expansion of PLA foams from 4.4 to 7.5–16.0. The addition of starch with content of 1–5 wt % further increased the LOI up to 30.6% and also endowed PLA/FR/St foams with improved antidripping properties. All these wonderful characteristics make the prepared PLA foams very promising for application in green packaging.
Co-reporter:Bin Shen, Dingding Lu, Wentao Zhai and Wenge Zheng
Journal of Materials Chemistry A 2013 vol. 1(Issue 1) pp:50-53
Publication Date(Web):03 Oct 2012
DOI:10.1039/C2TC00044J
We firstly report a facile approach to produce few-layered graphene sheets by low-temperature (130 °C) exfoliation and reduction of graphite oxide under ambient atmosphere with the aid of HCl. The obtained graphene materials exhibited high BET specific surface area (∼500 m2 g−1) and excellent electrical conductivity (∼1200 S m−1).
Co-reporter:Jianqiang Ling, Wentao Zhai, Weiwei Feng, Bin Shen, Jianfeng Zhang, and Wen ge Zheng
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 7) pp:2677
Publication Date(Web):March 6, 2013
DOI:10.1021/am303289m
We report a facile approach to produce lightweight microcellular polyetherimide (PEI)/graphene nanocomposite foams with a density of about 0.3 g/cm3 by a phase separation process. It was observed that the strong extensional flow generated during cell growth induced the enrichment and orientation of graphene on cell walls. This action decreased the electrical conductivity percolation from 0.21 vol % for PEI/graphene nanocomposite to 0.18 vol % for PEI/graphene foam. Furthermore, the foaming process significantly increased the specific electromagnetic interference (EMI) shielding effectiveness from 17 to 44 dB/(g/cm3). In addition, PEI/graphene nanocomposite foams possessed low thermal conductivity of 0.065–0.037 W/m·K even at 200 °C and high Young’s modulus of 180–290 MPa.Keywords: electrical conductivity; electromagnetic interference shielding; graphene; microcellular foam; polyetherimide;
Co-reporter:Bin Shen, Wentao Zhai, Mimi Tao, Jianqiang Ling, and Wenge Zheng
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 21) pp:11383
Publication Date(Web):October 17, 2013
DOI:10.1021/am4036527
Novel high-performance polyetherimide (PEI)/graphene@Fe3O4 (G@Fe3O4) composite foams with flexible character and low density of about 0.28–0.4 g/cm3 have been developed by using a phase separation method. The obtained PEI/G@Fe3O4 foam with G@Fe3O4 loading of 10 wt % exhibited excellent specific EMI shielding effectiveness (EMI SE) of ∼41.5 dB/(g/cm3) at 8–12 GHz. Moreover, most the applied microwave was verified to be absorbed rather than being reflected back, resulting from the improved impedance matching, electromagnetic wave attenuation, as well as multiple reflections. Meanwhile, the resulting foams also possessed a superparamagnetic behavior and low thermal conductiviy of 0.042–0.071 W/(m K). This technique is fast, highly reproducible, and scalable, which may facilitate the commercialization of such composite foams and generalize the use of them as EMI shielding materials in the fields of spacecraft and aircraft.Keywords: EMI shielding; foams; graphene@Fe3O4; polyetherimide; superparamagnetic;
Co-reporter:Guoying Ji, Wentao Zhai, Dongpo Lin, Qian Ren, Wenge Zheng, and Dong Won Jung
Industrial & Engineering Chemistry Research 2013 Volume 52(Issue 19) pp:6390
Publication Date(Web):April 22, 2013
DOI:10.1021/ie302281c
During the solid state foaming, the CO2 saturated poly(lactic acid) (PLA) sample at 5 MPa and 20 °C has a high crystallinity of 23.2%, and the prepared PLA foams exhibits low foam expansion and nonuniform cell structure. This study presents an interesting effect of nanosilica addition on the cell morphology and expansion ratio of PLA foams. It was found that the presence of nanosilica increased the induced crystallinity of PLA up to 29.7% at 5 MPa. The resultant PLA/silica foams exhibited significant and concurrent increase in cell structure uniformity and cell density: the cell density increased about 5–10 times, the expansion ratio increased 1.4–2.1 times, and the crystallinity of foams increased 1.3 times, compared to pure PLA foams. Further investigation suggested that the formation of the tiny crystallite size and the well dispersed nanosilica aggregates were thought as the main reasons to explain the interesting effect of nanosilica addition on the foaming behavior of PLA.
Co-reporter:Xiaoqin Lan, Wentao Zhai, and Wenge Zheng
Industrial & Engineering Chemistry Research 2013 Volume 52(Issue 16) pp:5655-5665
Publication Date(Web):March 26, 2013
DOI:10.1021/ie302899m
Polypropylene (PP) bead foams were prepared by autoclave foaming using n-pentane and CO2 as the blowing agents. PP foams blown with n-pentane had foaming temperatures of 92–96 °C, expansion ratios of 10–50 times, and a signal Tm at 150.1 °C, while PP foams blown with CO2 had foaming temperatures of 151–153 °C, expansion ratios of 8–20 times, and dual melting peaks at 164.0 and 140.9 °C. Polyethylene (PE) addition was used to improve the foaming behavior of PP and to induce the formation of dual and multiple Tm in PP/PE foams. A differential scanning calorimetry procedure was carried out to simulate the steam-chest molding of bead foams. Interbead bonding was found to be determined by the heat of fusion of Tmc (crystal melting of the newly formed crystals during fast cooling), ΔHmc. Recrystallization of the PE component contributed to the increase of ΔHmc, which potentially improved interbead bonding of the molded PP/PE bead foams.
Co-reporter:Wentao Zhai, Weiwei Feng, Jianqiang Ling, and Wenge Zheng
Industrial & Engineering Chemistry Research 2012 Volume 51(Issue 39) pp:12827-12834
Publication Date(Web):September 4, 2012
DOI:10.1021/ie3017658
Microcellular structure endows polymeric foams with the improved mechanical properties, but the preparation of lightweight microcellular polyimide (PI) foams with a large size is challenging and inefficient, because of low gas solubility, high stiffness, and an extremely long saturation time. In this study, PI foam was prepared by solid-state microcellular foaming technology with the compressed CO2 as a physical blowing agent and tetrahydrofuran as coblowing agent. The presence of coblowing agent was verified to increase the gas sorption of PI, causing a dramatic increase in the expansion ratio of microcellular PI beads from 2.9 to 15.7. Using a novel compression molding process, the prepared PI foams were molded into the 3-D shaped products. Before the molding, the foamed PI beads were coated by poly(ether imide) (PEI)/chloroform solution. The contact angle tests indicated that PEI/chloroform could infiltrate well PI foams’ surface, which facilitated the formation of strong interbead bonding between bead foams. The thickness of the coated PEI layer and the interbead bonding regions were the important parameters to adjust the bending and compression properties of the molded PI foam (MPI) product. The experimental results indicated that the bending strength and compression strength (at 10% strain) of MPI sample with density of 137.7 kg/m3 were 1.27 and 1.59 MPa, respectively.
Co-reporter:Bin Shen, Wentao Zhai, Dingding Lu, Jing Wang and Wenge Zheng
RSC Advances 2012 vol. 2(Issue 11) pp:4713-4719
Publication Date(Web):13 Apr 2012
DOI:10.1039/C2RA01098D
Poly(vinyl alcohol) (PVA) functionalized graphene (f-G) was prepared by ultrasonication of pristine graphene (p-G) in a PVA aqueous solution. PVA macroradicals formed by sonochemical degradation of the PVA solution were successfully trapped by graphene and grafted onto its surface. This was confirmed by transmission electron microscopy, atomic-force microscopy and 1H NMR measurements. The content of PVA on graphene was estimated to be ∼35%. The f-G could be well dispersed in the PVA matrix by a simple solution mixing and casting procedure. Due to the effective load transfer between f-G and PVA matrix, the mechanical properties of the f-G/PVA films were significantly improved. Compared with the p-G/PVA films, a 12.6% increase in tensile strength and a 15.6% improvement of Young's modulus were achieved by addition of only 0.3 wt% f-G. Moreover, our simple ultrasonication technique could enable us to functionalize graphene with other polymers.
Co-reporter:Bin Shen;Dingding Lu;Wenge Zheng;Qing Yan
Polymer International 2012 Volume 61( Issue 12) pp:1693-1702
Publication Date(Web):
DOI:10.1002/pi.4355
Abstract
Graphene has recently gained revolutionary aspirations because of its remarkable electronic, thermal and mechanical properties. These unique properties make it promising for preparing multifunctional nanocomposites. In recent years, polymer foams based on graphene have also received increasing attention in both the scientific and industrial communities. This review presents an overview of polymer/graphene nanocomposite foams discussing the production of graphene, the polymer functionalization of graphene and different polymer/graphene foams with different properties. One of the most promising avenues is to fabricate tough and lightweight materials with superior electrical and electromagnetic interference shielding properties. Copyright © 2012 Society of Chemical Industry
Co-reporter:Wentao Zhai;Jing Wang;Nan Chen;Hani E. Naguib;Chul B. Park
Polymer Engineering & Science 2012 Volume 52( Issue 10) pp:2078-2089
Publication Date(Web):
DOI:10.1002/pen.23157
Abstract
Poly(ethylene-co-octene)/multiwall carbon nanotube (PEOc/MWNT) nanocomposites were prepared by a melt blending process. The MWNT's solubility and the transmission electron microscopy (TEM) observation indicated that the MWNT bonded well with a PEOc matrix. This facilitated the orientation of the MWNT when shear and extensional forces were applied to the nanocomposite melts. Microcellular PEOc/MWNT nanocomposite foams were prepared by a rising temperature process using supercritical CO2 as the blowing agent. Various foaming times were selected to reveal the cell-structure evolution during the cell growth stage. The obvious cell opening, resulting from cell coalescence, was observed in the cell wall in the neat PEOc foams. When the MWNT was introduced, however, the MWNT tended to orient in the cell wall. Here, as a result of the strain hardening, it acted as a self-reinforcing element, protecting the cells from destruction during cell growth. Consequently, a dramatic decrease in the open cell content and a still high cell density at long foaming times were obtained in the PEOc/MWNT nanocomposite foams. The present study provides experimental evidence of the vital effects of nanoparticle orientation on cell coalescence. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers
Co-reporter:Bin Shen, Wentao Zhai, Cao Chen, Dingding Lu, Jing Wang, and Wenge Zheng
ACS Applied Materials & Interfaces 2011 Volume 3(Issue 8) pp:3103
Publication Date(Web):July 11, 2011
DOI:10.1021/am200612z
The effect of melt blending on the interaction between graphene and polystyrene (PS) matrix has been investigated in this paper. The interaction between graphene and PS was significantly enhanced by melt blending, which led to an increased amount of PS-functional graphene (PSFG) exhibiting good solubility in some solvents. The PS chains on PSFG could effectively prevent the graphene sheets from aggregating and the prepared PS/PSFG composites exhibited a homogeneous dispersion and an improved electrical property. The mechanism of melt blending on this enhanced interaction was attributed to the formation of π–π stacking during the melt blending. Moreover, the formation of chemical bonding during melt blending may have also enhanced the interaction.Keywords: graphene; interactions; melt blending; polystyrene; π−π stacking;
Co-reporter:Jing Wang, Wentao Zhai, Jianqiang Ling, Bin Shen, Wenge Zheng, and Chul B. Park
Industrial & Engineering Chemistry Research 2011 Volume 50(Issue 24) pp:13840-13847
Publication Date(Web):November 1, 2011
DOI:10.1021/ie201643j
The preparation of poly(lactic acid) (PLA) foam with a well-defined cell structure, high crystallinity, a high expansion ratio, and good mechanical properties is critical to its broader applications. However, achieving these properties in PLA foam simultaneously is challenging, because high crystallinity generally results in nonuniform cell nucleation and suppresses cell growth in the case of solid-state foaming. This study presents a novel approach using ultrasonic irradiation (UI) to achieve the desired properties in PLA simultaneously. As expected, CO2-saturated PLA samples at 5 MPa have a high crystallinity (23.4%), and foamed PLA samples at various foaming temperatures exhibit low foam expansion and nonuniform cell structure. By introducing UI at the very start of the foaming, however, the resultant PLA foams presented a significant and concurrent increase in cell structure uniformity and cell density: cell density increased about 2 orders of magnitude, the expansion ratio increased 1–2 times, the elongation at break increased 2 times, and the specific tensile strength increased 1.1 times, compared to samples without UI. Further investigation indicated that the enhanced cell nucleation induced by UI was the main reason for this unique phenomenon. Our study provides a simple but efficient and cost-effective method to fabricate PLA foams that possess excellent mechanical properties.
Co-reporter:Wentao Zhai;Chul B. Park
Polymer Engineering & Science 2011 Volume 51( Issue 12) pp:2387-2397
Publication Date(Web):
DOI:10.1002/pen.22011
Abstract
The goal of this study is to fabricate a soft foam with high cell density and high foam expansion based on thermoplastic polyolefin (TPO), and to supply a potential candidate for soft thermoset foams. It was found that a linear polypropylene (PP)-based TPO foam exhibited very poor cell morphology because of its weak melt strength. Nanoclay was introduced into the TPO to improve its foaming behavior. The extrusion foaming experiments demonstrated that the introduction of 0.5 wt% nanoclay significantly increased the cell morphology and expansion ratio of TPO/clay nanocomposite foams due to the enhanced cell nucleation and the possible cell coalescence suppression at low temperatures. At a high nanoclay content of 2.0 wt%, the cell density and foam expansion of foams increased continuously compared with the 0.5 wt% nanoclay addition. Our study suggested that it was possible to produce soft TPO foams with a well-defined cell structure and high foam expansion using a continuous method, but that a proper PEOc content control was needed to maximize foam expansion. POLYM. ENG. SCI., 2011. ©2011 Society of Plastics Engineers.
Co-reporter:Bin Shen, Yang Li, Da Yi, Wentao Zhai, Xingchang Wei, Wenge Zheng
Carbon (March 2017) Volume 113() pp:
Publication Date(Web):March 2017
DOI:10.1016/j.carbon.2016.11.034
Strong flexible polymer/graphene composite films with ideal electromagnetic interference (EMI) shielding are fabricated through constructing a sandwich structure consisting of polyester non-woven fabric as reinforcing interlayer and thermoplastic polyurethane (TPU) composite with high graphene loading as conductive coating layer. The engineered sandwich film (defined as TPU/G film) with graphene loading of ∼20 wt% and total coating thickness of ∼50 μm not only possesses excellent mechanical flexibility and strong strength, but also exhibits qualified bandwidth of shielding effectiveness (SE) ≥ 20 dB as wide as ∼49.1 GHz in a broadband frequency range of 5.4–59.6 GHz. Moreover, saw-tooth folding of the flexible TPU/G films could efficiently enhance the shielding performance, and more conductive folded film with smaller included angle plus longer side would result in much greater SE enhancement along with reduced EM reflection. This finding also realizes the convenient performance regulation of the folded TPU/G films through a simple mechanical deformation, showing promise for tunable EMI shielding.Strong flexible polymer/graphene composite films with ideal electromagnetic interference (EMI) shielding are fabricated through constructing a sandwich structure consisting of polyester non-woven fabric as reinforcing interlayer and thermoplastic polyurethane (TPU) composite with high graphene loading as conductive coating layer. The engineered sandwich film (defined as TPU/G film) with graphene loading of ∼20 wt% and total coating thickness of ∼50 μm not only possesses excellent mechanical flexibility and strong strength, but also exhibits qualified bandwidth of shielding effectiveness (SE) ≥ 20 dB as wide as ∼49.1 GHz in a broadband frequency range of 5.4–59.6 GHz. Moreover, saw-tooth folding of the flexible TPU/G films could efficiently enhance the shielding performance, and more conductive folded film with smaller included angle plus longer side would result in much greater SE enhancement along with reduced EM reflection. This finding also realizes the convenient performance regulation of the folded TPU/G films through a simple mechanical deformation, showing promise for tunable EMI shielding.
Co-reporter:Yang Li, Bin Shen, Da Yi, Lihua Zhang, Wentao Zhai, Xingchang Wei, Wenge Zheng
Composites Science and Technology (18 January 2017) Volume 138() pp:
Publication Date(Web):18 January 2017
DOI:10.1016/j.compscitech.2016.12.002
Multilayered thermoplastic polyurethane/graphene (PUG) composites were fabricated by stacking single-layered PUG foams together. The arrangement of single-layered PUG foams in different orders could realize the gradient concentration of graphene, which was proved to be a facile approach to enhance the microwave-absorbing (MA) property of PUG composites, rather than their electromagnetic interference (EMI) shielding effectiveness (SE). Further sandwiching a wave-transmitting layer between two pieces of PUG foams formed a sandwich structure, by which the SE of the two samples could be significantly improved and the resultant composites still possessed strong MA performance. The SE increment was assigned to the enhanced reflection loss induced by constructive interference, and largely dependent on the thickness of the interlayer d. Particularly, when the values of the d were zero and the quarter of the largest wavelength in the testing frequency range, the minimum and maximum SE could be obtained, respectively. These results are critical to the fabrication of high-performance polymer-based shielding materials with strong MA property.
Co-reporter:Zhuang Zhang, Guangming Chen, Hanfu Wang and Wentao Zhai
Journal of Materials Chemistry A 2015 - vol. 3(Issue 8) pp:NaN1654-1654
Publication Date(Web):2015/01/16
DOI:10.1039/C4TC02471K
A new strategy, i.e. interfacial adsorption-soft template polymerization, is developed to enhance polymer thermoelectric property. The obtained nanocomposite 3D interconnected architecture consisting of reduced graphene oxide (rGO) nanolayers sandwiched by polypyrrole (PPy) nanowires is directly confirmed by scanning and transmission electron microscopies. Moreover, the nanocomposites reveal significantly enhanced thermoelectric performance. At rGO:PPy ratio of 50 wt%, the nanocomposite power factor reaches ∼476.1 times that of pure PPy nanowires. Our results suggest that a greatly enhanced thermoelectric property for polymer nanocomposites can be achieved by a complex morphology design.
Co-reporter:Bin Shen, Dingding Lu, Wentao Zhai and Wenge Zheng
Journal of Materials Chemistry A 2013 - vol. 1(Issue 1) pp:NaN53-53
Publication Date(Web):2012/10/03
DOI:10.1039/C2TC00044J
We firstly report a facile approach to produce few-layered graphene sheets by low-temperature (130 °C) exfoliation and reduction of graphite oxide under ambient atmosphere with the aid of HCl. The obtained graphene materials exhibited high BET specific surface area (∼500 m2 g−1) and excellent electrical conductivity (∼1200 S m−1).