Effect of Pulp Chamber Access, Instrumentation, Obturation, and Restoration on the Fracture Resistance of Endodontically Treated Canine Teeth in Dogs.

Veterinary studies documenting the effect of endodontic treatment on tooth fracture resistance are scarce. The objective of this ex vivo study was to evaluate the effects of mesial access preparation and restoration, as well as pulp chamber access, instrumentation, obturation, and restoration, on the fracture resistance and characteristics of canine teeth in dogs. Sixty-five dog canine teeth were divided into 4 groups: 1. Standard endodontic treatment through a mesial access only; 2. Treatment as per group 1, adding an incisal access, instrumentation and obturation of the pulp chamber, and restoration of the access; 3. Treatment as per group 2, without pulp chamber obturation or restoration of the incisal access; and 4. Untreated teeth. The fracture resistance and characteristics of each group were documented using axial compression testing, angled 45° disto-occlusal to the long axis of the crown. The maximum force prior to fracture in groups 1, 3, and 4 were not statistically different, demonstrating that restored mesial and incisal accesses with pulp chamber instrumentation did not statistically affect fracture resistance. However, obturated and restored group 2 teeth demonstrated decreased fracture resistance compared to all other groups (P < .001). Additionally, 26.7% of group 1 teeth sustained complicated crown fractures, while 100% of group 2 teeth fractured within the obturation or restorative materials, preventing pulp exposure in these cases. Although the cause and clinical importance of decreased tooth fracture resistance following pulp chamber obturation and restoration remains unknown, it may provide protective value for maintaining a coronal seal in the event of tooth fracture.

Direct 3D Printing of Hybrid Nanofiber-Based Nanocomposites for Highly Conductive and Shape Memory Applications.

Three-dimensional (3D) printing with conductive polymer nanocomposites provides an attractive strategy for the "on-demand" fabrication of electrical devices. This paper demonstrates a family of highly conductive multimaterial composites that can be directly printed into ready-to-use multifunctional electrical devices using a flexible solvent-cast 3D printing technique. The new material design leverages the high aspect ratio and low contact resistance of the hybrid silver-coated carbon nanofibers (Ag@CNFs) with the excellent 3D printability of the thermoplastic polymer. The achieved nanocomposites are capable of printing in open air under ambient conditions, meanwhile presenting a low percolation threshold (i.e., <6 vol %) and high electrical conductivity (i.e., >2.1 × 105 S/m) without any post-treatments. We further find that this hybrid Ag@CNF-based nanocomposite shows a quick and low-voltage-triggered electrical-responsive shape memory behavior, making it a great candidate for printing electroactive devices. Multiple different as-printed Ag@CNF-based highly conductive nanocomposite structures used as high-performance electrical devices (e.g., ambient-printable conductive components, microstructured fiber sensors, flexible and lightweight scaffolds for electromagnetic interference shielding, and low-voltage-triggered smart grippers) are successfully demonstrated herein. This simple additive manufacturing approach combined with the synergic effects of the multimaterial nanocomposite paves new ways for further development of advanced and smart electrical devices in areas of soft robotics, sensors, wearable electronics, etc.

3D Printing of Highly Conductive Nanocomposites for the Functional Optimization of Liquid Sensors.

The utilization of 3D printing of highly conductive (σ ≈ 2350 S m-1 ) polymer composite structures for the functional optimization of scaffold-shaped liquid sensors is demonstrated. This study can open the pathway of the application of 3D printing of conductive composites for optimization of structures useful for various applications such as smart sensors in textile or in the field of electronics.

Helical and Dendritic Unzipping of Carbon Nanotubes: A Route to Nitrogen-Doped Graphene Nanoribbons.

Bamboo structured nitrogen-doped multiwalled carbon nanotubes (CN(x)-MWCNTs) have been successfully unzipped by a chemical oxidation route, resulting in nitrogen-doped graphene nanoribbons (CN(x)-GNRs) with a multifaceted microstructure. The oxidation of CN(x)-MWCNTs was carried out using potassium permanganate in the presence of trifluoroacetic acid or phosphoric acid. On the basis of the high resolution transmission electron microscopy studies, the bamboo compartments were unzipped via helical or dendritic mechanisms, which are different from the longitudinal unzipping of open channel MWCNTs. The product graphene oxide nanoribbons were simultaneously reduced and doped with nitrogen by thermal annealing in an ammonia atmosphere. The effects of the annealing temperature, time, and atmosphere on the doping level and types of the nitrogen functional groups have been investigated. X-ray photoelectron spectroscopy results indicate that a wide range of doping levels can be achieved (4-9 at %) simply by changing the annealing conditions. Pyridinic and pyrrolic nitrogen functional groups were the dominant species that were attached to the edges of the CN(x)-GNRs. The GNRs, with a faceted structure and pyridinic and pyrrolic groups on their edges, have abundant nitrogen sites. These active sites could play a vital role in enhancing the electrocatalytic performance of GNRs.

3D analysis of the morphology and spatial distribution of nitrogen in nitrogen-doped carbon nanotubes by energy-filtered transmission electron microscopy tomography.

We present here the application of the energy-filtered transmission electron microscopy (EFTEM) in the tomographic mode to determine the precise 3D distribution of nitrogen within nitrogen-doped carbon nanotubes (N-CNTs). Several tilt series of energy-filtered images were acquired on the K ionization edges of carbon and nitrogen on a multiwalled N-CNT containing a high amount of nitrogen. Two tilt series of carbon and nitrogen 2D maps were then calculated from the corresponding energy-filtered images by using a proper extraction procedure of the chemical signals. Applying iterative reconstruction algorithms provided two spatially correlated C and N elemental-selective volumes, which were then simultaneously analyzed with the shape-sensitive reconstruction deduced from Zero-Loss recordings. With respect to the previous findings, crucial information obtained by analyzing the 3D chemical maps was that, among the two different kind of arches formed in these nanotubes (transversal or rounded ones depending on their morphology), the transversal arches contain more nitrogen than do the round ones. In addition, a detailed analysis of the shape-sensitive volume allowed the observation of an unexpected change in morphology along the tube axis: close to the round arches (with less N), the tube is roughly cylindrical, whereas near the transversal ones (with more N), its shape changes to a prism. This relatively new technique is very powerful in the material science because it combines the ability of the classical electron tomography to solve 3D structures and the chemical selectivity of the EFTEM imaging.

Nitrogen-doped carbon nanotubes as a highly active metal-free catalyst for selective oxidation.

Catalytic reactions are generally carried out on supported metals or oxides, which act as an active phase and require impregnation and thermal treatment steps. During tests, the metal or oxide nanoparticles could be further sintered, which would induces deactivation. Direct incorporation of the active phase into the matrix of a support could be an elegant alternative to prevent catalyst deactivation. Here, we report that nitrogen-doped carbon nanotubes (N-CNTs) can be efficiently employed as a metal-free catalyst for oxidative reactions that allow the selective transformation of the harmful, gaseous H(2)S into solid sulfur. The catalyst exhibits a high stability during the test at high space velocity. The macroscopic shaping of the catalyst on the silicon carbide foam also increases its catalytic activity by improving the contact between the reactants and the catalyst. Such macroscopic shaping allows the avoidance of problems linked with transport and handling of nanoscopic materials and also reduces the pressure drop across the catalyst bed to a large extent.