Enhancement of fracture toughness of epoxy nanocomposites by combining nanotubes and nanosheets as fillers

In this work the fracture toughness of epoxy resin has been improved through the addition of low loading of single part and hybrid nanofiller materials. Functionalised multi-walled carbon nanotubes (f-MWCNTs) was used as single filler, increased the critical strain energy release rate, GIC, by 57% compared to the neat epoxy, at only 0.1 wt% filler content. Importantly, no degradation in the tensile or thermal properties of the nanocomposite was observed compared to the neat epoxy. When two-dimensional boron nitride nanosheets (BNNS) were added along with the one-dimensional f-MWCNTs, the fracture toughness increased further to 71.6% higher than that of the neat epoxy. Interestingly, when functionalised graphene nanoplatelets (f-GNPs) and boron nitride nanotubes (BNNTs) were used as hybrid filler, the fracture toughness of neat epoxy is improved by 91.9%. In neither of these hybrid filler systems the tensile properties were degraded, but the thermal properties of the nanocomposites containing boron nitride materials deteriorated slightly

Improving the fracture toughness properties of epoxy using graphene nanoplatelets at low filler content

This paper reports improvement in the fracture properties of epoxy nanocomposites using plasma functionalized graphene nanoplatelets (f-GNP) at low filler content. Various mechanical tests were performed on a series of f-GNP/epoxy at low nanofiller loading to assess the effect of the nanofiller on mechanical properties. Most importantly, a significant enhancement in fracture toughness is achieved without compromising the tensile and thermal properties of the nanocomposites. The fracture toughness of neat epoxy resin was increased by over 50% with the incorporation of 0.25 wt% f-GNP loading, obtaining a value of 245 J m−2, while the neat epoxy indicated a value of 162 J m−2. The glass transition temperature (Tg) and coefficient of thermal expansion (CTE) both showed a slight increase of 3% and 2%, respectively, both at 1 wt% f-GNP loading. These enhancements are competitive with current literature results on nanocomposites, but at significantly lower filler content. We therefore demonstrate that f-GNPs are capable of providing effective toughening of epoxy resins, while maintaining other tensile and thermal properties

Excitons at the B K edge of boron nitride nanotubes probed by x-ray absorption spectroscopy

We have performed a near-edge x-ray absorption fine-structure (NEXAFS) investigation of multi-walled boron nitride nanotubes (BNNTs). We show that the one-dimensionality of BNNTs is clearly evident in the B K edge spectrum, while the N K edge spectrum is similar to that of layered hexagonal BN (h-BN). We observe a sharp feature at the Ã* onset of the B K edge, which we ascribe to a core exciton state. We also report a comparison with spectra taken after an ammonia plasma treatment, showing that the B K edge becomes indistinguishable from that of h-BN, due to the breaking of the tubular order and the formation of small h-BN clusters

Improving the mechanical properties of graphene oxide based materials by covalent attachment of polymer chains

We report on the modification of graphene oxide (GO) with poly(vinyl alcohol) (PVA) leading to the mechanical improvement of GO based materials. First, GO was covalently functionalised with PVA by esterification of carboxylic groups on GO with hydroxyl groups of PVA resulting in functionalised f-(PVA)GO. This was carried out for PVA of six different molecular weights. This functionalised graphene oxide could be formed into a paper-like material by vacuum filtration. Papers prepared from f-(PVA)GO showed significant increases in mechanical properties compared to those prepared with GO or with simple mixtures of GO and PVA. The best performance was achieved for PVA functional groups with molecular weights between 50 and 150 kg/mol. Improvements in Young’s moduli of 60% and tensile strength of 400% were observed relative to GO-only paper. The improved mechanical properties are attributed to enhanced inter-flake stress transfer due to the covalently bonded PVA. Second, functionalised f-(PVA)GO was used as filler in * Corresponding author. Tel/Fax: +34 976 73-3977 / -3318. E-mail address: [email protected] (W.K. Maser) 2 PVA-based composites. The application of a pre-selection method allowed the use of only the largest functionalised f-(PVA)GO flakes. This resulted in substantially reinforced PVA-f-(PVA)GO composites. Both modulus and strength increased by 40% relative to the pure polymer for f- (PVA)GO loadings below 0.3 vol.%.The authors would like to acknowledge Science Foundation Ireland, (grant number 07/IN.7/I1772), Spanish Ministry of Science and Innovation (MICINN) under project MAT2010-15026, Spanish Research Council CSIC under project 201080E124 and the Government of Aragon (DGA) under Project DGA-T66 CNN. M.C. thanks MICINN for her PhD contract and funding for research stay at TCD under FPI Programme BES-2008-003503.Peer reviewe

Covalent Carbene Functionalization of Graphene: Toward Chemical Band-Gap Manipulation

In this work, we employ dibromocarbene (DBC) radicals to covalently functionalize solution exfoliated graphene via the formation of dibromocyclopropyl adducts. This is achieved using a basic aqueous/organic biphasic reaction mixture to decompose the DBC precursor, bromoform, in conjunction with a phase-transfer catalyst to facilitate ylide formation and carbene migration to graphene substrates. DBC-functionalized graphene (DBC-graphene) was characterized using a range of spectroscopic and analytical techniques to confirm the covalent nature of functionalization. Modified optical and electronic properties of DBC-graphene were investigated using UV–vis spectroscopy, analysis of electrical <i>I</i>–<i>V</i> transport properties, and noncontact terahertz time-domain spectroscopy. The implications of carbene functionalization of graphene are considered in the context of scalable radical functionalization methodologies for bulk-scale graphene processing and controlled band-gap manipulation of graphene

Oxygen Radical Functionalization of Boron Nitride Nanosheets

The covalent chemical functionalization of exfoliated hexagonal boron–nitride nanosheets (BNNSs) is achieved by the solution-phase oxygen radical functionalization of boron atoms in the h-BN lattice. This involves a two-step procedure to initially covalently graft alkoxy groups to boron atoms and the subsequent hydrolytic defunctionalization of the groups to yield hydroxyl-functionalized BNNSs (OH-BNNSs). Characterization of the functionalized-BNNSs using HR-TEM, Raman, UV–vis, FTIR, NMR, and TGA was performed to investigate both the structure of the BNNSs and the covalent functionalization methodology. OH-BNNSs were used to prepare polymer nanocomposites and their mechanical properties analyzed. The influence of the functional groups grafted to the surface of the BNNSs is investigated by demonstrating the impact on mechanical properties of both noncovalent and covalent bonding at the interface between the nanofiller and polymer matrixes

Dibromocarbene Functionalization of Boron Nitride Nanosheets: Toward Band Gap Manipulation and Nanocomposite Applications

We report the covalent functionalization of exfoliated boron nitride nanosheets (BNNSs) using dibromocarbene (DBC) species. The functionalization of BNNSs is enabled as the nanosheets are utilized as two-dimensional phase-transfer catalysts for the migration of carbenes across the organic–aqueous phase boundary. We postulate that BNNSs stabilize carbenes by forming B-CBr₂ ylides and in turn act as the reaction substrate. DBC functionalization of BNNSs results in the formation of B–C and B–N bonds to the sp²-hybridized BNNS lattice via the formation of dibromo-bridged bicyclo BCN systems. The covalent functionalization was characterized using HR-TEM, AFM, EELS, XRD, EDX, ToF-SIMS, TGA, Raman, XPS, FTIR, and UV–vis techniques. Utilization of CBr₂ groups as a means by which BNNSs may be integrated and interfaced with solvents, molecular species, and condensed-phase materials was demonstrated by grafting alkyl chains from the functional groups via alkyl/halogen exchange. Alkyl-functionalized BNNSs were integrated within polyethylene (LDPE) and extruded to form BNNS-nanocomposite fibers. Implications of the covalent functionalization of h-BN are considered in the context of band gap manipulation and the versatility of the CBr₂ functional groups to enable subsequent chemical derivatization

Targeting DNA Replication before it Starts: Cdc7 as a Therapeutic Target in p53-Mutant Breast Cancers

Treatment options for triple-receptor negative (ER−/PR−/Her2−) and Her2-overexpressing (ER−/PR−/Her2+) breast cancers with acquired or de novo resistance are limited, and metastatic disease remains incurable. Targeting of growth signaling networks is often constrained by pathway redundancy or growth-independent cancer cell cycles. The cell-cycle protein Cdc7 regulates S phase by promoting DNA replication. This essential kinase acts as a convergence point for upstream growth signaling pathways and is therefore an attractive therapeutic target. We show that increased Cdc7 expression during mammary tumorigenesis is linked to Her2-overexpressing and triple-negative subtypes, accelerated cell cycle progression (P < 0.001), arrested tumor differentiation (P < 0.001), genomic instability (P = 0.019), increasing NPI score (P < 0.001), and reduced disease-free survival (HR = 1.98 [95% CI: 1.27–3.10]; P = 0.003), thus implicating its deregulation in the development of aggressive disease. Targeting Cdc7 with RNAi, we demonstrate that p53-mutant Her2-overexpressing and triple-negative breast cancer cell lines undergo an abortive S phase and apoptotic cell death due to loss of a p53-dependent Cdc7-inhibition checkpoint. In contrast, untransformed breast epithelial cells arrest in G1, remain viable, and are able to resume cell proliferation on recovery of Cdc7 kinase activity. Thus, Cdc7 appears to represent a potent and highly specific anticancer target in Her2-overexpressing and triple-negative breast cancers. Emerging Cdc7 kinase inhibitors may therefore significantly broaden the therapeutic armamentarium for treatment of the aggressive p53-mutant breast cancer subtypes identified in this study