(1) Aim: To investigate the effect of synthetic bone substitutes, α-tricalcium phosphate (α-TCP) or bi-layered biphasic calcium-phosphate (BBCP) combined with deproteinized bovine bone mineral (DBBM), on bone formation. (2) Methods: Thirty critical size defects were randomly treated with the following five different treatment modalities: (1) negative control (NC, empty), (2) DBBM, (3) α-TCP + DBBM (1:1), (4) BBCP 3%HA/97%α-TCP + DBBM (1:1), and (5) BBCP 6%HA/94%α-TCP + DBBM (1:1). The samples, at four weeks post-surgery, were investigated by micro-CT and histological analysis. (3) Results: A similar level of new bone formation was demonstrated in the DBBM with α-TCP bone substitute groups when compared to the negative control by histomorphometry. DBBM alone showed significantly lower new bone area than the negative control (p = 0.0252). In contrast to DBBM, the micro-CT analysis revealed resorption of the α-TCP + DBBM, BBCP 3%HA/97%α-TCP + DBBM and BBCP 6%HA/94%α-TCP + DBBM, as evidenced by a decrease of material density (p = 0.0083, p = 0.0050 and p = 0.0191, respectively), without changing their volume. (4) Conclusions: New bone formation was evident in all defects augmented with biomaterials, proving the osteoconductive properties of the tested material combinations. There was little impact of the HA coating degree on α-TCP in bone augmentation potential and material resorption for four weeks when mixed with DBBM. 相似文献
Smart hydrogels hold much potential for biocatalysis, not only for the immobilization of enzymes, but also for the control of enzyme activity. We investigated upper critical solution temperature-type poly N-acryloyl glycinamide (pNAGA) hydrogels as a smart matrix for the amine transaminase from Bacillus megaterium (BmTA). Physical entrapment of BmTA in pNAGA hydrogels results in high immobilization efficiency (>89 %) and high activity (97 %). The temperature-sensitiveness of pNAGA is preserved upon immobilization of BmTA and shows a gradual deswelling upon temperature reduction. While enzyme activity is mainly controlled by temperature, deactivation tended to be higher for immobilized BmTA (≈62–68 %) than for free BmTA (≈44 %), suggesting a deactivating effect due to deswelling of the pNAGA gel. Although the deactivation in response to hydrogel deswelling is not yet suitable for controlling enzyme activity sufficiently, it is nevertheless a good starting point for further optimization. 相似文献
Electrostatic potential barriers at doped ZnO-ZnO interfaces can be modified by stress-induced polarization charges. This concept was enhanced by preparing ZnO-based single crystal-polycrystal-single crystal structures by diffusion bonding. Increasing time for epitaxial solid-state transformation results in structures with a decreasing thickness of residual polycrystalline material in between two well-oriented single crystals. Microstructural and electrical analysis quantifies the influence of high-temperature treatment during epitaxial growth on the stress sensitivity of the prepared structures. The orientation of the single crystals is defined to maximize the interaction between stress-induced polarization charges and the potential barriers at doped ZnO-ZnO interfaces. With decreasing thickness of residual polycrystalline material, the percentage of grain boundaries with favorably aligned polarization vectors is increased resulting in a higher stress sensitivity. This effect is compensated by an adverse effect of the high-temperature treatment on the initial potential barrier height. Hence, a maximum in stress sensitivity can be observed for intermediate times of epitaxial growth. The prepared structures close the gap between the varistor piezotronics based on bulk ceramics with random orientation of the polarization vector and the bicrystal piezotronics with perfect orientation of the polarization vector, demonstrating the capability of microstructural engineering for varistor-based piezotronic devices. 相似文献
Studies of the electrochemical oxidation of a series of straight-chain terminal alkenoic acids adsorbed at a Pt(111) electrode surface are reported. Compounds adsorbed were: propenoic acid (acrylic acid, PPA); 3-butenoic acid (vinylacetic acid, 3BTA); 4-pentenoic acid (allylacetic acid, 4PTA); 6-heptenoic acid (6HPA); and 10-undecenoic acid (10UDA). Vibrational spectra of adsorbed layers were obtained by use of electron energy-loss spectroscopy (EELS). Molecular packing densities were measured by use of Auger spectroscopy. Electrochemical oxidation of each adsorbed layer was explored by means of cyclic voltammetry in aqueous inert electrolyte (KF/HF). As the analogous aliphatic acids are not chemisorbed at Pt under the same conditions, the alkenoic acids evidently adsorb at Pt(111) predominantly through the C=C double bond. Molecular packing densities indicate that the carboxylic acid moiety is in contact with the Pt surface only in the case of PPA. EELS spectra also indicate that the carboxylate groups (other than in PPA) are present as pendants. The carboxylic acid O-H stretching bands of most of the adsorbed acids are red-shifted and broadened, evidently due to extensive intermolecular hydrogen bonding; the exceptions are PPA, for which the interaction is primarily with the Pt surface, and 3BTA, for which intermolecular interaction between the carboxylic acid pendants is apparently prevented by steric considerations. The surface-attached carboxylic acid moieties react with KOH solution, leading to retention of K+ ions, detected by Auger spectroscopy, and to changes in the vibrational spectra indicative of carboxylate anions; reactivity toward KOH decreases with chain length. Adsorbed alkenoic acids at Pt(111) surfaces are stable in water and in vacuum. Oxidation of the adsorbed short-chain acids PPA and 3BTA proceeds to completion, forming CO2 as the principal product. Oxidation of the adsorbed long-chain acids converts the C=C moiety to 2CO2, and transforms the remainder of the molecule to an unadsorbed diacid (likely possibilities are malonic acid from 4PTA; glutaric acid from 6HPA; and heptane-1,7-dioic acid from 10UDA). 相似文献
Functionally reconfigurable general purpose parallel machines (FRPM) could be reconfigured during the operation from SIMD to MIMD mode or vice versa (first aspect) and from one interconnection network to another according to the data storing order (second aspect). General purpose machines are considered in order to obtain an arbitrary data exchange between the processing elements they are built of. A model for describing such interconnection networks is presented. A full-information exchange network in introduced which is reconfigurable in a programming way to tree-, matrix-, cube-, linear-neighbourhood and FFT-network. Some schemes for constructing SIMD/MIMD reconfigurable machines are given. The usefullness of using FRMP for image processing and pattern recognition is discussed. 相似文献
This paper introduces a new type of fuzzy inference systems, denoted as dynamic evolving neural-fuzzy inference system (DENFIS), for adaptive online and offline learning, and their application for dynamic time series prediction. DENFIS evolve through incremental, hybrid (supervised/unsupervised), learning, and accommodate new input data, including new features, new classes, etc., through local element tuning. New fuzzy rules are created and updated during the operation of the system. At each time moment, the output of DENFIS is calculated through a fuzzy inference system based on m-most activated fuzzy rules which are dynamically chosen from a fuzzy rule set. Two approaches are proposed: (1) dynamic creation of a first-order Takagi-Sugeno-type fuzzy rule set for a DENFIS online model; and (2) creation of a first-order Takagi-Sugeno-type fuzzy rule set, or an expanded high-order one, for a DENFIS offline model. A set of fuzzy rules can be inserted into DENFIS before or during its learning process. Fuzzy rules can also be extracted during or after the learning process. An evolving clustering method (ECM), which is employed in both online and offline DENFIS models, is also introduced. It is demonstrated that DENFIS can effectively learn complex temporal sequences in an adaptive way and outperform some well-known, existing models 相似文献
Here, we present the performance of a thermoelectric (TE) module consisting of n-type (La0.12Sr0.88)0.95TiO3 and p-type Ca3Co4?xO9+δ materials. The main challenge in this investigation was operating the TE module in different atmospheric conditions, since n-type has optimum TE performance at reducing conditions, while p-type has optimum at oxidizing conditions. The TE module was exposed to two different atmospheres and demonstrated higher stability in N2 atmosphere than in air. The maximum electrical power output decreased after 40 h when the hot side was exposed to N2 at 600°C, while only 1 h at 400°C in ambient air was enough to oxidize (La0.12Sr0.88)0.95TiO3 followed by a reduced electrical power output. The module generated maximum electrical power of 0.9 mW (~?4.7 mW/cm2) at 600°C hot side and δT?~?570 K in N2, and 0.15 mW (~?0.8 mW/cm2) at 400°C hot side and δT?~?370 K in air. A stability limit of Ca3Co3.93O9+δ at ~?700°C in N2 was determined by in situ high-temperature x-ray diffraction.
The sensitivity toward mechanical stress of barium titanate-based positive temperature coefficient resistor material was investigated by determining the resistance change with application of uniaxial stress from room temperature to 200 °C, which is well above the Curie temperature TC. Using the Landau–Ginsburg–Devonshire theory the resistance increases in the paraelectric state, the negligible impact of stress close to TC and the observed increase in TC with increasing stress could be rationalized. For the ferroelectric state, the stress-related resistance increase was attributed to ferroelasticity, a change in bulk permittivity and interfacial stress inducing a piezoelectric potential. The obtained results are also discussed with respect to recent endeavors to tune properties of potential barriers in piezoelectric semiconductors by mechanical stress. 相似文献