Bonding Strength (bonding + strength)

Distribution by Scientific Domains

Kinds of Bonding Strength

  • hydrogen bonding strength


  • Selected Abstracts


    Bonding strength between a hard chairside reline resin and a denture base material as influenced by surface treatment

    JOURNAL OF ORAL REHABILITATION, Issue 12 2001
    C. R. Leles
    Direct relining of dentures made with hard chairside reline resins is faster than laboratory-processed reline systems and the patient is not without the prosthesis for the time necessary to perform the laboratory procedures. However, a weak bond between the autopolymerizing acrylic reline resins and the denture base material has been observed. This study evaluated the effect of six different surface treatments on the bond strength between a hard chairside reline acrylic resin and a heat-cured acrylic resin. Specimens of the heat-cured acrylic resin were divided into seven groups. One of these groups remained intact. In the other groups, a 10-mm square section was removed from the centre of each specimen. The bonding surfaces were then treated with (i) methyl methacrylate monomer, (ii) isobutyl methacrylate monomer, (iii) chloroform, (iv) acetone, (v) experimental adhesive and (vi) no surface treatment , control group. Kooliner acrylic resin was packed into the square sections and polymerized. The bonding strength was evaluated by a three-point loading test. The results were submitted to one-way analysis of variance (ANOVA) followed by a Tukey multiple range test at a 5% level of significance. No significant difference was found between the surface treatment with Lucitone 550 monomer or chloroform, but both were stronger than the majority of the other groups. The bond strength provided by all the surface treatments was lower than that of the intact heat-cured resin. [source]


    Dentin surface treatment using a non-thermal argon plasma brush for interfacial bonding improvement in composite restoration

    EUROPEAN JOURNAL OF ORAL SCIENCES, Issue 5 2010
    Andy C. Ritts
    Ritts AC, Li H, Yu Q, Xu C, Yao X, Hong L, Wang Y. Dentin surface treatment using a non-thermal argon plasma brush for interfacial bonding improvement in composite restoration. Eur J Oral Sci 2010; 118: 510,516. © 2010 Eur J Oral Sci The objective of this study was to investigate the treatment effects of non-thermal atmospheric gas plasmas on dentin surfaces used for composite restoration. Extracted unerupted human third molars were prepared by removing the crowns and etching the exposed dentin surfaces with 35% phosphoric acid gel. The dentin surfaces were treated using a non-thermal atmospheric argon plasma brush for various periods of time. The molecular changes of the dentin surfaces were analyzed using Fourier transform infrared spectrophotometry/attenuated total reflectance (FTIR/ATR), and an increase in the amount of carbonyl groups was detected on plasma-treated dentin surfaces. Adper Single Bond Plus adhesive and Filtek Z250 dental composite were applied as directed. To evaluate the dentin/composite interfacial bonding, the teeth thus prepared were sectioned into micro-bars and analyzed using tensile testing. Student,Newman,Keuls tests showed that the bonding strength of the composite restoration to peripheral dentin was significantly increased (by 64%) after 30 s of plasma treatment. However, the bonding strength to plasma-treated inner dentin did not show any improvement. It was found that plasma treatment of the peripheral dentin surface for up to 100 s resulted in an increase in the interfacial bonding strength, while prolonged plasma treatment of dentin surfaces (e.g. 5 min) resulted in a decrease in the interfacial bonding strength. [source]


    Multi-walled Carbon Nanotube-Reinforced Hydroxyapatite Layers on Ti6Al4V Medical Implants by Electrophoretic Deposition (EPD),

    ADVANCED ENGINEERING MATERIALS, Issue 1-2 2008
    C. Kaya
    Sol-gel synthesised nano-size hydroxyapatite (HA) powders were dispersed in water-based suspensions with the addition of multi-walled carbon nanotubes. Ti6Al4V medical alloys were coated with monolithic and carbon nanotube-reinforced HA using electrophoretic deposition (EPD) in an attempt to control deposit structure and thickness. It was shown that the sintering temperature of the deposited HA layers was significantly lowered by the use of sinter active nano-powders. Moreover the addition of carbon nanotubes increased the bonding strength of the EPD-formed layers to the metallic substrate. The cost-effective EPD technique used in the present work has high industrial potential for coating metallic medical implants with composite bioactive layers. [source]


    Comparative study on the nonadditivity of methyl group in lithium bonding and hydrogen bonding

    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 5 2009
    Qingzhong Li
    Abstract Quantum chemical calculations at the second-order Moeller,Plesset (MP2) level with 6-311++G(d,p) basis set have been performed on the lithium-bonded and hydrogen-bonded systems. The interaction energy, binding distance, bond length, and stretch frequency in these systems have been analyzed to study the nonadditivity of methyl group in the lithium bonding and hydrogen bonding. In the complexes involving with NH3, the introduction of one methyl group into NH3 molecule results in an increase of the strength of lithium bonding and hydrogen bonding. The insertion of two methyl groups into NH3 molecule also leads to an increase of the hydrogen bonding strength but a decrease of the lithium bonding strength relative to that of the first methyl group. The addition of three methyl groups into NH3 molecule causes the strongest hydrogen bonding and the weakest lithium bonding. Although the presence of methyl group has a different influence on the lithium bonding and hydrogen bonding, a negative nonadditivity of methyl group is found in both interactions. The effect of methyl group on the lithium bonding and hydrogen bonding has also been investigated with the natural bond orbital and atoms in molecule analyses. © 2008 Wiley Periodicals, Inc. Int J Quantum Chem, 2009 [source]


    Influence of solid lubricant reinforcement on wear behavior of Kevlar fabric composites

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008
    Fang Guo
    Abstract The friction and wear behavior of Kevlar fabric composites reinforced by PTFE or graphite powders was investigated using a Xuanwu-III friction and wear tester at dry sliding condition, with the unfilled Kevlar fabric composite as a reference. The worn surfaces were analyzed by means of scanning electron microscope, and X-ray photoelectron spectroscopy. It was found that PTFE or graphite as fillers could significantly improve the tribological behavior of the Kevlar fabric composites, and the Kevlar fabric composites filled with 20% PTFE exhibited the best antiwear and antifriction ability among all evaluated cases. The transfer films established with two lubricants in sliding wear of composites against metallic counterparts made contributions to reducing friction coefficient and wear rate of Kevlar fabric composites. In particular, FeF2 generated in the sliding of Kevlar fabric composites filled with PTFE against counterpart pin improved the bonding strength between the transfer film and counterpart surface, which accounted for the lowest friction coefficient and wear rate of the Kevlar fabric composites filled with PTFE measured in the testing. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008. [source]


    The influence of the impregnating chemicals on the bonding strength of impregnated wood materials

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008
    Ayhan Özçifçi
    Abstract In this study, it is aimed to determine the bonding strength of white oak (Quercus petreae L.) and chestnut (Castanea sativa Mill.) woods impregnated with borax and zinc chloride. Within this purpose, the experimental samples were bonded with Polyvinyl-acetate and polyurethane based Desmodur-VTKA (D-VTKA) adhesives according to BS EN 205 standards after they had been prevacuumed with a pressure equal to 760 mmHg,1 with impregnating at 2 atm pressures for 60 min according to ASTM-D 1413 standards and applied vacuum-impregne-vacuum method. During the experiments, the retention amount, the retention proportion, and the bonding strength values of the samples were determined. According to the test results, the highest values of retention amount, and bonding strength were obtained from the wood material impregnated with zinc chloride. The impregnating materials had a negative effect on bonding strength. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]


    Using collision-induced dissociation with corrections for the ion number of degrees of freedom for quick comparisons of relative bonding strength

    JOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 11 2004
    Natalia Vinokur
    Abstract The number of degrees of freedom-dependent stability of ions and ion,neutral non-covalent complexes under collision-induced dissociation (CID) conditions was studied in a quadrupole ion trap mass spectrometer. It was found that the stability of ions as probed by energy-variable CID has a linear dependence on the total number of degrees of freedom for the ions (or ion,neutral complexes) with the same (or nearly the same) bonding energy. The slope of such a stability vs number of degrees of freedom dependence correlates with the binding energy. Proton-bound amine dimers display the lowest slope as they have weak bonds. Breaking covalent bonds will result in much greater slopes. In addition to the binding energy, the vibrational frequencies of the ion also affect the stability vs number of degrees of freedom behavior. Studying such a dependence of the CID stability in a system paves the way for direct relative binding energy comparisons. The application of this approach is demonstrated by testing the relative heme affinities of anti-malaria drugs and related compounds. Copyright © 2004 John Wiley & Sons, Ltd. [source]


    Hydrogen bonding strength,measures based on geometric and topological parameters,

    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 1 2004
    awomir Janusz Grabowski
    Abstract Different methods of estimating H-bond strength are presented. The studies are based on the results of MP2/6,311++G** calculations and the binding energies are corrected for the basis set superposition error (BSSE). The wavefunctions were further applied to localize bond critical points and ring critical points. The characteristics based on the Bader theory are also applied as indicators and measures of hydrogen bonding. This study compares samples of different compounds. The H-bond strength measures such as the proton,acceptor distance (H···Y), the length of the proton donating bond, the electron density at H···Y bond critical point, the H-bond energy and others are analysed. The case of the intramolecular hydrogen bonding is also analysed, and its special characteristics are given. Copyright © 2003 John Wiley & Sons, Ltd. [source]


    The Relationship Between Multiple Scratch Tests and Wear Behavior of Hot-Pressed Silicon Nitride Ceramics with Various Rare-Earth Additive Systems

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2008
    Hideki Hyuga
    The wear behavior of Si3N4 ceramics sintered with various rare earth additives was studied for nonlubricated sliding under different conditions, and scratch tests carried out in an attempt to correlate the wear behavior. When multiple scratch testing is used the results can be used to indicate the initial wear behavior under fracture-dominated wear of the materials. The additive system used in the sintering of the Si3N4 ceramics affected the specific wear rate under nonlubricated sliding conditions, and under high load conditions, where fracture is dominant, the specific wear rate was shown to increase in samples sintered with lutetium as a consequence of a strong bonding strength between the grains and grain boundary resulting in a higher degree of brittle fracture. [source]


    Orthodontic brackets removal under shear and tensile bond strength resistance tests , a comparative test between light sources

    LASER PHYSICS LETTERS, Issue 3 2008
    P.C.G. Silva
    Abstract We have investigated if a new LEDs system has enough efficient energy to promote efficient shear and tensile bonding strength resistance under standardized tests. LEDs 470 ± 10 nm can be used to photocure composite during bracket fixation. Advantages considering resistance to tensile and shear bonding strength when these systems were used are necessary to justify their clinical use. Forty eight human extracted premolars teeth and two light sources were selected, one halogen lamp and a LEDs system. Brackets for premolar were bonded through composite resin. Samples were submitted to standardized tests. A comparison between used sources under shear bonding strength test, obtained similar results; however, tensile bonding test showed distinct results: a statistical difference at a level of 1% between exposure times (40 and 60 seconds) and even to an interaction between light source and exposure time. The best result was obtained with halogen lamp use by 60 seconds, even during re-bonding; however LEDs system can be used for bonding and re-bonding brackets if power density could be increased. (© 2008 by Astro Ltd., Published exclusively by WILEY-VCH Verlag GmbH & Co. KGaA) [source]


    The comparison of wear properties of different Fe-based hardfacing alloys in four kinds of testing methods

    LUBRICATION SCIENCE, Issue 4 2008
    E. Badisch
    Abstract Iron-based hardfacing alloys are widely used to protect machinery equipment. A strong correlation is given between microstructure and chemical composition of welding deposit with the resulting wear behaviour. Concerning precipitation of metallurgical hard phases and synthetic added hard particles, the bonding strength of the hard phases in the metallic matrix seems to play a dominating role to obtain high wear resistance. The main objective of this study was to evaluate the wear behaviour for pure abrasion, combined impact/abrasion and high impact wear, respectively, for four different Fe-based hardfacing alloys. Tests were performed with a standard ASTM G65 dry-sand/rubber-wheel tester. An impeller,tumbler apparatus enabled investigation of impact abrasion wear tests. Additional wear tests with high impact loading were performed on a drop hammer apparatus. Fracture surface analysis was carried out after drop hammer testing and results were correlated with microstructure and interfacial bonding behaviour of precipitations in metallic matrix. Copyright © 2008 John Wiley & Sons, Ltd. [source]


    Pressure-Sensitive Adhesive Blend Films for Low-Tack Applications

    MACROMOLECULAR MATERIALS & ENGINEERING, Issue 7 2007
    Peter Müller-Buschbaum
    Abstract Polymer blend films consisting of a tacky and a nonadhesive component are promising candidates for low-tack applications. Immiscibility of both components results in a phase separation process yielding a tacky matrix with glassy objects embedded. The influence of the blending ratio of the components poly(n -butyl acrylate) (PnBA) and polystyrene (PS) is addressed. The mechanical information resulting from the tack test shows the possibility of varying the bonding strength of the PSA blend over a wide range. The macroscopic and microscopic structural characterization with optical microscopy and ultrasmall angle X-ray scattering (USAXS) shows that the blend PnBA/PS exhibits similarities to common filler systems as well as deviates regarding installed structures. Due to the large domain size on a microscopic level, only the tacky component, PnBA, defines the adhesive behavior. The nonadhesive component limits the contact area between the adhesive and the substrate. [source]


    Covalent addition of diethyltoluenediamines onto carbon nanotubes for composite application

    POLYMER COMPOSITES, Issue 8 2009
    Shiren Wang
    Diethyltoluenediamines (DETDA) was grafted to single-walled carbon nanotubes (SWNTs) through diazonium-based addition for improving dispersion and interfacial bonding in SWNT/epoxy nanocomposites. Characterization results of Fourier Transformed Infrared spectroscopy and Raman spectroscopy validated covalent bonding between DETDA and carbon nanotubes. The degree of functionalization was about 4% based on thermo-gravimetric analysis. Interfacial bonding strength was computed in the presence of chemical bonding and the computation results indicated that the interfacial shear strength in the presence of functionalized carbon nanotubes was significantly enhanced. The experimental test revealed that the tensile strength of nanocomposites was enhanced about 23% and Young's modulus about 25%, with 0.5 wt% loading of functionalized-nanotubes. These considerable improvements further verified the load-transfer enhancement in the functionalized-SWNTs/epoxy nanocomposites. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source]


    Hydrogen bond-mediated self-assembly and supramolecular structures of diblock copolymer mixtures

    POLYMER INTERNATIONAL, Issue 5 2009
    Shiao-Wei Kuo
    Abstract This review summarizes recent advances in the preparation of hydrogen bonding block copolymer mixtures and the supramolecular structures they form through multiple hydrogen bonding interactions. Hydrogen bonding in block copolymer mixtures that form nanostructures and have unusual electronic, photonic and magnetic properties is a topic of great interest in polymer science. Combining the self-assembly of block copolymers with supramolecular structures offers unique possibilities to create new materials with tunable and responsive properties. The self-assembly of structures from diblock copolymer mixtures in the bulk state is readily controlled by varying the weight fraction of the block copolymer mixture and the copolymer composition; in solution, the morphologies are dependent on the copolymer composition, the copolymer concentration, the nature of the common solvent, the amount of the selective solvent and, most importantly, the hydrogen bonding strength. Copyright © 2008 Society of Chemical Industry [source]


    Degradation of high barrier ethylene,vinyl alcohol copolymer under mild thermal-oxidative conditions studied by thermal analysis and infrared spectroscopy

    POLYMER INTERNATIONAL, Issue 6 2001
    José M Lagaron
    Abstract A study of the thermal-oxidative degradation of a high barrier ethylene,vinyl alcohol copolymer with 32,mol% of ethylene (EVOH) has been carried out by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and Fourier-transform infrared spectroscopy (FTIR) under mild temperature conditions above melting. It was found that time exposures of up to 11,h at temperatures between 9 and 33,°C above the EVOH melting point resulted in polymer weight losses of up to 3.6% with colour formation. The weight loss was faster at short times and slowed down with increasing exposure time. DSC showed a small decrease in crystallinity and melting point, melting-peak broadening and a slight increase in the glass transition temperature of the samples subjected to the more severe thermal-oxidative treatment. The FTIR experiments showed transformation of the vinyl alcohol hydroxyl groups into carbonyl groups and creation of double bonds. Changes in degradation kinetics and perhaps in mechanisms are thought to occur with increasing exposure time. Moreover, FTIR measurements suggest that transformation of the hydroxyl groups leads to a weakening of the overall hydrogen bonding strength in the degraded samples, and therefore a reduction in intermolecular cohesion can be anticipated. © 2001 Society of Chemical Industry [source]