Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Compressive Strength”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 37 records · Page 2Linked to original sources

Setting reactions and compressive strengths of calcium phosphate cements.

Setting reactions and compressive strengths of a self-hardening calcium phosphate cement (CPC) were investigated. The CPC consists of tetracalcium phosphate (TTCP) and anhydrous dicalcium phosphate (DCPA). The cement specimens were prepared by mixing 0.7 g of the powder (TTCP 72.9 wt% + DCPA 27.1 wt%) with 0.175 mL of the liquid (25 mmol/L H3PO4 and 1.32 mmol/L sodium fluoride). The specimens were removed from the molds at pre-determined time intervals after being mixed, and their compressive strengths were measured. Immediately afterward, the fractured specimens were rapidly frozen in ethanol (-80 degrees C), lyophilized, and examined by powder x-ray diffraction and scanning electron microscopy (SEM). The results showed that (1) hydroxyapatite was the only reaction product; (2) the reaction was nearly completed within four h, during which both the reaction product and compressive strength increased linearly with time, resulting in a strong correlation between the two; and (3) fully set CPC consisted primarily of small rod-like crystals and some platy crystals.

Calcium Phosphates↗

Prediction of the compressive strength of human lumbar vertebrae.

The compressive strength of 98 specimens of motion segments of human thoracolumbar spines was measured. In addition, the density of the trabecular bone in the midplane of the vertebrae was assessed by quantitative computed tomography (QCT); the size of the vertebral endplates was measured by CT as well. The results show that the compressive strength of thoracolumbar vertebrae can be predicted from the product of density and end-plate area, with an error of estimate of 1 kN. The data of the experiment allow for an in vivo prediction of the strength of vertebrae to quantify the risk of fracture in physically very demanding tasks, to support expert opinion in trauma cases, or to assist in therapeutic decisions in cases of severe osteoporosis.

Humans↗

Effect of mixing methods on the compressive strength of glass ionomer cements.

OBJECTIVE: The purpose of the study was to evaluate the effect of the mixing method on the compressive strength and porosity of dental glass ionomer cements. METHOD: Five glass ionomer cements were chosen for use in the study. Two were hand mixed and three were encapsulated. The latter were mixed either by shaking or rotating. Following mixing by rotation some samples were centrifuged before use. The 24h compressive strength was determined for each cement/mixing regime combination and fracture surfaces were examined using SEM. RESULTS: The mixing method had a significant effect on compressive strength (P<0.05). For the luting/lining cement, hand mixing produced a significantly greater compressive strength (P<0.05). For the restorative cement, there were only small differences between specimens mixed by different methods and hand mixing gave a significantly lower compressive strength than mixing by rotation followed by centrifuging (P<0.05). Porosity was incorporated in all samples and low values of compressive strength were associated with larger pores. SIGNIFICANCE: The strength of glass ionomer cements is affected by incorporated porosity and this is dependent on the method of mixing. For some cements hand mixing is favoured in order to reduce porosity and increase strength but this is not generally applicable to all cements.

Capsules↗

The effect of mixing time on the handling and compressive strength of an encapsulated glass-ionomer cement.

OBJECTIVES: The effects of varying mixing times on the properties of glass-ionomer cements have been poorly investigated, and many clinicians are uninformed about the potential changes in handling achieved by this. This study aims to explore the effects of mixing time variation. METHODS: An experimental glass-ionomer system was dosed into a capsule, activated, and triturated for varying lengths of time, from 2 to 14 s. Measurements were made of working time, initial setting time, compressive strength and compressive modulus, and a subjective assessment of handling conducted. RESULTS: The working time and initial setting time decreased as mixing time increased, while compressive strength and compressive modulus increased to a maximum at 12 s mixing time. The material essentially pre-gelled after 14 s of mixing, which resulted in breaking of the gel matrix and poorer properties. SIGNIFICANCE: Clinicians should feel confident, within limits, of varying mixing times of glass ionomer cements to improve properties or to slow the reaction.

Compressive Strength↗

A synthetic aragonite-based bioceramic: influence of process parameters on porosity and compressive strength.

We investigate the influence of process parameters such as weight fraction and particle size of pore-former, and isostatic pressure, on porosity and compressive strength of non-sintered porous calcium carbonate biomaterials compacted at high pressure in uniaxial or isostatic mode. Experiment design and results analysis are performed according to a two-level 2k factorial design method (FDM). Results indicate that only the weight fraction of pore-former (wt fpf) influences significantly the porosity and the compressive strength. The porosity P, is described by a linear function of wt fpf, and the compressive strength sigma(comp), by an exponential one. For materials compacted under uniaxial pressing: P (vol%) = 33.7 + 85.4 (wt fpf) and sigma(comp) (MPa) = 28.8e(-9.2(wt fpf)) with 0.1 < or = wt fpf < or = 0.3. For materials compacted in isostatic mode: P (vol%) = 33.9 + 82.1 (wt fpf) and sigma(comp) (MPa) = 24.0e(-7.0(wt fpf)) with 0.15 < or = wt fpf < or = 0.35. The pore-former particle size has no significant influence on both properties. The increase in isostatic pressure provides slightly lower porosity and better compressive strength. For a fixed fraction of pore-former, isostatic pressing leads to a better compressive strength than uniaxial pressing. This study indicates that, for a constant amount of pore former, the size of macropores can be adjusted to reach optimal bone-ingrowth without change in compressive strength.

Biocompatible Materials↗

Depth of cure and compressive strength of dental composites cured with blue light emitting diodes (LEDs).

OBJECTIVE: The primary objective of this pilot study was to test the hypotheses that (i) depth of cure and (ii) compressive strength of dental composites cured with either a light emitting diode (LED) based light curing unit (LCU) or a conventional halogen LCU do not differ significantly. The second objective of this study was to characterise irradiance and the emitted light spectra for both LCUs to allow comparisons between the units. METHODS: Dental composite (Spectrum TPH, shades A2 and A4) was cured for 40 s with either a commercial halogen LCU or a LED LCU, respectively. The LED LCU uses 27 blue LEDs as the light source. The composites' depth of cure was measured for 10 samples of 4 mm diameter and 8 mm depth for each shade with a penetrometer. The results were compared using a Student's t-test. Compressive strengths were determined after 6 and 72 h, for six samples of 4 mm diameter and 6 mm depth for each shade after being polymerised for 40 s from each end of the mould. Groups were compared using a three way ANOVA. RESULTS: The conventional halogen LCU cured composites significantly (p < 0.05) deeper (6.40 mm A2, 5.19 mm A4) than did the LED LCU (5.33 mm A2, 4.27 mm A4). Both units cured the composite deeper than required by both ISO 4049 and the manufacturer. A three way ANOVA showed that there were no significant differences in the compressive strengths of samples produced with either the LED LCU or the halogen LCU (p = 0.460). Significant differences in compressive strength of samples stored for 6 and 72 h (p = 0.0006) and of samples of different shades (p = 0.035) were found as confirmed by the three way ANOVA. The light spectra of both units differed strongly. While the halogen LCU showed a broad distribution of wavelengths with a power peak at 497 nm, the LED LCU emitted most of the generated light at 465 nm. The LED LCU produced a total irradiance of 350 mW cm-2 whereas the halogen LCU produced a total irradiance of 755 mW cm-2. SIGNIFICANCE: The results showed that both units provided sufficient output to exceed minimum requirements in terms of composites' depth of cure according to ISO 4049 and the depth of cure and the composites' compressive strength stated by the manufacturer. Compressive strengths of dental composites cured under laboratory conditions with a LED LCU were statistically equivalent to those cured with a conventional halogen LCU. With its inherent advantages, such as a constant power output over the lifetime of the diodes, LED LCUs have great potential to achieve a clinically consistent quality of composite cure.

Analysis of Variance↗

Compressive strength of some polyalkenoates with or without dental amalgam alloy incorporation.

The present study compares the compressive strength after one week of some conventional glass-ionomer restorative materials with that of glass ionomers reinforced by the addition of ceramic-coated silver or dental amalgam alloy particles to the aluminosilicate glass powder. Apart from the commercially available Ketac Silver and Miracle Mix, experimental mixtures of Fuji II glass-ionomer powder, the old as well as the new version, with various amounts of either a spherical or lathe-cut amalgam alloy were investigated. For the conventional glass ionomers, the mean compressive strength based on all measurements amounts to 159.9 +/- 4.5 MPa. Both formulations of Fuji II have a comparable strength after one-week maturation. The compressive strength of Ketac Silver does not differ significantly from that of Ketac Fill or from that of the conventional glass ionomers investigated. The effect of admixing amalgam alloy on the compressive strength is found to be determined by the shape and the amount of the alloy particles. Moreover, both parameters are interactive with the formulation of the Fuji glass ionomer used for preparation of the mixture. The results indicate that when dental amalgam alloy is added to the glass ionomer, lathe-cut particles are to be preferred but only in an amount up to 20% by weight.

Analysis of Variance↗

Segmental stability and compressive strength of posterior lumbar interbody fusion implants.

STUDY DESIGN: Human cadaveric study on initial segmental stability and compressive strength of posterior lumbar interbody fusion implants. OBJECTIVES: To compare the initial segmental stability and compressive strength of a posterior lumbar interbody fusion construct using a new cortical bone spacer machined from allograft to that of titanium threaded and nonthreaded posterior lumbar interbody fusion cages, tested as stand-alone and with supplemental pedicle screw fixation. SUMMARY OF BACKGROUND DATA: Cages were introduced to overcome the limitations of conventional allografts. Radiodense cage materials impede radiographic assessment of the fusion, however, and may cause stress shielding of the graft. METHODS: Multisegmental specimens were tested intact, with posterior lumbar interbody fusion implants inserted into the L4/L5 interbody space and with supplemental pedicle screw fixation. Three posterior lumbar interbody fusion implant constructs (Ray Threaded Fusion Cage, Contact Fusion Cage, and PLIF Allograft Spacer) were tested nondestructively in axial rotation, flexion-extension, and lateral bending. The implant-specimen constructs then were isolated and compressed to failure. Changes in the neutral zone, range of motion, yield strength, and ultimate compressive strength were analyzed. RESULTS: None of the stand-alone implant constructs reduced the neutral zone. Supplemental pedicle screw fixation decreased the neutral zone in flexion-extension and lateral bending. Stand-alone implant constructs decreased the range of motion in flexion and lateral bending. Differences in the range of motion between stand-alone cage constructs were found in flexion and extension (marginally significant). Supplemental posterior fixation further decreased the range of motion in all loading directions with no differences between implant constructs. The Contact Fusion Cage and PLIF Allograft Spacer constructs had a higher ultimate compressive strength than the Ray Threaded Fusion Cage. CONCLUSIONS: The biomechanical data did not suggest any implant construct to behave superiorly either as a stand-alone or with supplemental posterior fixation. The PLIF Allograph Spacer is biomechanically equivalent to titanium cages but is devoid of the deficiencies associated with other cage technologies. Therefore, the PLIF Allograft Spacer is a valid alternative to conventional cages.

Bone Screws↗

An evaluation of elastomeric impression materials based on surface compressive strength.

The setting times of seven commercially available elastomeric impression materials were determined using Wilson's reciprocating rheometer at temperatures 23 +/- 0.5 or 32 +/- 0.5 degrees C. The surface compressive strength and depression of these materials after setting time were measured using a rheometer (Fudoh). Each material was mixed according to the mixing proportion (base/accelerator or catalyst ratio) recommended by the manufacturer. The surface compressive strength and the depression of each material were measured by using a method which pressed the material to the edge of a sensitive rod (2.0 mm in diameter) connected to a load cell. In the case of silicone impression materials (additional type) at a temperature of 23 +/- 0.5 degrees C, the surface compressive strength and the depression of these materials were extremely stable after the setting time. However, the surface compressive strength of other materials except additional type materials increased markedly after setting time and the depression corresponding to the surface compressive strength decreased. These increased largely with the increase, in pressing speed to the sensitive rod. At 450 s from the setting time of all materials, there was an adequate correlation (r = 0.84) between measured values and theoretical values derived using the theory of elasticity.

Compressive Strength↗

[Application of slightly acidic hypochlorous acid water to the dental field--setting expansion and compressive strength of dental gypsum mixed with slightly acidic hypochlorous acid water].

PURPOSE: This study investigated both the setting expansion and compressive strength of dental gypsum mixed with slightly acidic hypochlorous acid water for the prevention of hospital infection. METHODS: Slightly acidic hypochlorous acid water (PURESTER Mp-240B, Morinaga Milk Industry) was used to mix each of three types of gypsum (model plaster, dental stone and high strength dental stone), and both the setting expansion and compressive strength of these gypsum products were analyzed in comparison with those mixed with tap water. RESULTS: 1. With regard to the setting expansion, a significant difference was not observed between gypsum products mixed with the two types of water, except for both the model plaster and dental stone 30 minutes after the start of mixing. 2. Regarding the compressive strength, a significant difference was not observed between gypsum products mixed with the two types of water, except for the model plaster 90 minutes after the start of mixing. CONCLUSIONS: From the results of the study, it was revealed that both the setting expansion and compressive strength of gypsum products using the slightly acidic hypochlorous acid water showed almost the same characteristics as those using tap water.

Calcium Sulfate↗

Compressive strength and surface characterization of glass ionomer cements modified by particles of bioactive glass.

OBJECTIVES: The aim of this study was to determine compressive strength, Young's modulus of elasticity, and Vickers' surface hardness, of conventional cure and resin-modified glass ionomer cements after the addition of bioactive glass (BAG) particles into the cements. METHODS: Experimental glass ionomer cement (GIC)-BAG materials were made by mixing 10- or 30-wt% of BAG particles with conventional cure and resin-modified GIC powders. Materials were processed into cylindrical specimens and immersed in water for 1, 3, 7, 14, 30 and 180 days before mechanical tests. SEM and EDS analysis was used to characterize the changes in surface topography and the main elemental composition. RESULTS: The compressive strength of the test specimens decreased with the increasing amount of BAG. The compressive strength of resin-modified GIC increased during the immersion, but remained at a lower level than that of the other materials. The conventional cure GIC-based materials had on average 55% higher surface microhardness than the resin-modified materials. In the elemental composition, more Ca was detected in the BAG-containing materials than in the pure GICs. The amount of F was significantly higher (p < 0.001) on all resin-modified materials, being highest on resin-modified GIC with 30-wt% of BAG after 180d of immersion. SIGNIFICANCE: The addition of BAG to GIC compromises the mechanical properties of the materials to some extent. Thus, their clinical use ought to be restricted to applications where their bioactivity can be beneficial, such as root surface fillings and liners in dentistry, and where high compressive strength is not necessarily needed.

Analysis of Variance↗

One-hour compressive strength of dental amalgam.

The one-hour compressive strength of 22 commercially available dental amalgams has been measured. Large differences between different alloys were observed. It was recognized that an intermediate one-hour compressive strength is probably the most desirable in view of the other properties which are involved.

Dental Alloys↗

The compressive strength of articular cartilage.

Articular cartilage provides the smooth bearing surfaces in freely moving (synovial) joints. Its mechanical properties are important because structural failure of cartilage is closely associated with joint disorders, including osteoarthritis. Some mechanical properties of cartilage are well characterized, but little is known about its compressive strength. A technique for measuring cartilage compressive strength is evaluated, and an overview of experiments which relate strength to stiffness and tissue hydration is given. Specimens of bovine articular cartilage-on-bone, approximately 15 mm square, were loaded on a hydraulic materials testing machine using flat impermeable indentors. Linear-ramp loading/unloading cycles of 1 s duration, and of increasing severity, were applied until failure was evident on force-displacement graphs. Some specimens were tested following a 30 min period of creep loading. Inkstaining and histology were used to locate the site of initial damage to each specimen. Specimen failure occurred first in the cartilage surface layer at a nominal applied stress of 14-59 MPa (mean 35.7 MPa). Mechanical properties were little affected by specimen or indentor size, provided both remained within defined limits, and compressive strength could be measured to an accuracy of approximately +/- 5 per cent. Compressive stiffness was a significant predictor of strength, but only if it was measured at high levels of stress. Strength increased following creep-induced water loss, and initial mechanical damage could propagate under moderate cyclic loading. This technique for measuring cartilage compressive strength has potential for investigating the causes of cartilage failure in vivo.

Animals↗

A comparison of the compressive strength of calcium hydroxide based lining materials.

This in vitro study investigated the compressive strength of five commercially available calcium hydroxide based lining materials and a resin bonded zinc oxide/eugenol material under varying conditions of temperature and relative humidity and at various ++time intervals after mixing. The results of the study showed that the calcium hydroxide liners could be consistently ranked in order with Dycal most frequently having the highest and either Life or Renew having the lowest compressive strength at all time intervals examined. Under simulated clinical conditions all the materials tested with the exception of Life and Renew had sufficient compressive strength 3 minutes after mixing to withstand the force of amalgam condensation.

Calcium Hydroxide↗

Estimating the compressive strength of the porcine cervical spine: an examination of the utility of DXA.

STUDY DESIGN: The failure strength of porcine spinal units was correlated with vertebral size and bone mineralization. The accuracy of the resulting predictive equations was tested with an independent sample of spinal units. OBJECTIVES: To determine if dual energy x-ray absorptiometry (DXA)-obtained measures of bone mineralization can be used to accurately predict the compressive tolerance of porcine spinal units. SUMMARY OF BACKGROUND DATA: Porcine spinal units are often used in place of cadaveric tissues, and normalization is used to improve the transferability of model results. In compressive testing, normalization can be performed to the estimated compressive strength. Bone mineralization measures have been shown to be positively correlated with compressive tolerance and have been used to predict the tolerance of human spinal units. However, the accuracy of these predictive equations has not been assessed with an independent sample. METHODS: Twenty porcine cervical spinal units were scanned (DXA) to obtain measures of bone mineral content (BMC) and bone mineral density (BMD). The units were compressed to failure, and the failure loads were correlated with the measured bone mineralization and endplate area of the spinal unit. The regression equations were used to predict the compressive tolerance of an independent sample of spinal units. RESULTS: BMC (P = 0.078) and BMD (P = 0.2834) were not significantly correlated to compressive strength. Endplate area was the most highly correlated variable, with an r of 0.5329. The use of a predictive equation including BMC on the second independent sample resulted in errors of estimation of 1.4 +/- 1.2 kN, corresponding to 13% of the average compressive strength. In comparison, the use of an equation employing endplate area alone resulted in estimation errors of 11%. CONCLUSIONS: Measures of BMC/BMD did not enhance predictions of compressive strength and will not reduce errors in compressive load normalization in a porcine model. The poor correlations found between BMC and compressive strength may be due to the non-load-bearing anterior processes of the porcine cervical spine.

Absorptiometry, Photon↗

Thermocycling--the effects upon the compressive strength and abrasion resistance of three composite resins.

The purpose of this investigation was to examine the effects of thermocycling upon the compressive strength and abrasive wear resistance of three commercial composites Fulfil, P-50 and Herculite-XR. Specimens of each material were divided into five treatment groups comprising a control, and four different cycling and storage regimes. Tests for compressive strength and wear resistance were carried out. Prior to testing all specimens were stored in distilled water for 1 week. Three groups were stored at a temperature of 37 degrees C and the remaining two at 60 degrees C. Thereafter all groups that were thermocycled were subjected to 750 cycles of a thermocycling regime consisting of the cycle ACAB where A and B represent the fixed temperatures of 37 degrees C and 5 degrees C, and C, depending upon the treatment group, either 50 degrees C or 60 degrees C. One-way analyses of variance upon the compressive strength and wear factor data following the treatments highlighted significant differences in the mean compressive strength for all materials (Fulfil (P < 0.05), P-50 and Herculite-XR (P < 0.01)) and in the wear factor values for only Fulfil and P-50 (P < 0.001). Surprisingly, thermocycling P-50 with an upper temperature limit of 50 degrees C had catastrophic consequences upon the measured properties. It is concluded that some of the observed behaviour may have potentially detrimental consequences upon the long-term clinical durability of the materials tested.

Analysis of Variance↗

Hardness and compressive strength of indirect composite resins: effects of immersion in distilled water.

The aim of this study was to evaluate the effect of ageing in distilled water on the hardness and compressive strength of a direct composite resin Z100, a feldspatic porcelain (Noritake) and three indirect composites (Artglass, Solidex and Targis). For the Vickers hardness tests, five disk-shaped specimens (2 x 4 mm) of each material were prepared according to the manufacturers' instructions. The hardness tests were conducted using a Vickers diamond indentor. Compressive strength measurements were recorded on cylindrical specimens with a diameter of 6 mm and a length of 12 mm. The compression tests were carried out with a constant cross-head speed of 0.5 mm min(-1) on a mechanical test machine. For each material, 10 specimens were tested after 7 days of dry storage at 37 +/- 1 degrees C and 10 specimens were tested after water storage at 37 +/- 1 degrees C for 180 days. Noritake porcelain specimens showed higher hardness values than the composites. Among the composite materials, Z100 promoted the highest VHN values, regardless of the ageing periods. The results showed that Solidex and Z100 had the highest compressive strength values. Ageing in water reduced the hardness for all composites, but had no long-term effect on the compressive strength.

Composite Resins↗

[The study of compressive strength of phosphate-bonded investment materials].

OBJECTIVE: The purpose of this study was to compare the compressive strength of phosphate-bonded investments. METHODS: The three sorts of investments were mixed according to manufacturer's recommendation before poured in the molds. After heated up to 900 degrees C, every sample was mounted on a universal experimental machine to test its compressive strength in ambient. RESULTS: Significant differences were found between the four groups(P < 0.01). CONCLUSION: From the data above it is concluded that the compressive strength of X-20 Chrome Investment mixed with the special liquid was the highest.

Compressive Strength↗