Analytical and Experimental Investigation of a Curved Piezoelectric Energy Harvester.

Piezoelectric energy harvesters have traditionally taken the form of base excited cantilevers. However, there is a growing body of research into the use of curved piezoelectric transducers for energy harvesting. The novel contribution of this paper is an analytical model of a piezoelectric energy harvesting curved beam based on the dynamic stiffness method (DSM) and its application to predict the measured output of a novel design of energy harvester that uses commercial curved transducers (THUNDER TH-7R). The DSM predictions are also verified against results from commercial finite element (FE) software. The validated results illustrate the resonance shift and shunt damping arising from the electrical effect. The magnitude, phase, Nyquist plots, and resonance frequency shift estimates from DSM and FE are all in satisfactory agreement. However, DSM has the advantage of having significantly fewer elements and is sufficiently accurate for commercial curved transducers used in applications where beam-like vibration is the predominant mode of vibration.

An in vitro evaluation of orthodontic aligner biomechanics around the maxillary arch.

INTRODUCTION: The objective of this study was to evaluate the forces and moments exerted by orthodontic aligners on 3 different displaced maxillary teeth and their adjacent supporting teeth. METHODS: An in vitro orthodontic simulator was used to measure the forces and moments of a 0.75-mm thick glycol-modified polyethylene terephthalate material for 3 maxillary teeth: central incisor, canine, and second premolar. Forces and moments were recorded for tested teeth displaced lingually one by one for 0.20 mm. Repeated measures of multivariate analysis of variance was used to assess the outcome. RESULTS: The mean buccolingual force applied on a displaced canine (2.25 ± 0.38 N) was significantly (P <0.001) more than the central incisor (1.49 ± 0.18 N) and second premolar (1.50 ± 0.16 N). The mean moment (that tends to tip the teeth buccally) exerted on a canine (-20.11 ± 5.27 Nmm) was significantly more (P <0.001) than the central incisor (-8.42 ± 1.67 Nmm) and second premolar (-11.45 ± 1.29 Nmm). The forces and moments acting on teeth adjacent to the displaced tooth were clinically significant and acted in opposing directions to those on the displaced tooth. CONCLUSIONS: The results of this study highlighted that for the same amount of displacement on a given tooth, the forces and moments imposed by the orthodontic aligner depend on location around the arch. These findings highlight the need to further study aligner mechanics around the dental arch and optimize aligner design to impose desired mechanical loads to avoid detrimental effects during orthodontic tooth movement.

Cell Wall Loosening in the Fungus, Phycomyces blakesleeanus.

A considerable amount of research has been conducted to determine how cell walls are loosened to produce irreversible wall deformation and expansive growth in plant and algal cells. The same cannot be said about fungal cells. Almost nothing is known about how fungal cells loosen their walls to produce irreversible wall deformation and expansive growth. In this study, anoxia is used to chemically isolate the wall from the protoplasm of the sporangiophores of Phycomyces blakesleeanus. The experimental results provide direct evidence of the existence of chemistry within the fungal wall that is responsible for wall loosening, irreversible wall deformation and elongation growth. In addition, constant-tension extension experiments are conducted on frozen-thawed sporangiophore walls to obtain insight into the wall chemistry and wall loosening mechanism. It is found that a decrease in pH to 4.6 produces creep extension in the frozen-thawed sporangiophore wall that is similar, but not identical, to that found in frozen-thawed higher plant cell walls. Experimental results from frozen-thawed and boiled sporangiophore walls suggest that protein activity may be involved in the creep extension.

Stiff mutant genes of phycomyces affect turgor pressure and wall mechanical properties to regulate elongation growth rate.

Regulation of cell growth is paramount to all living organisms. In plants, algae and fungi, regulation of expansive growth of cells is required for development and morphogenesis. Also, many sensory responses of stage IVb sporangiophores of Phycomyces blakesleeanus are produced by regulating elongation growth rate (growth responses) and differential elongation growth rate (tropic responses). "Stiff" mutant sporangiophores exhibit diminished tropic responses and are found to be defective in at least five genes; madD, E, F, G, and J. Prior experimental research suggests that the defective genes affect growth regulation, but this was not verified. All the growth of the single-celled stalk of the stage IVb sporangiophore occurs in a short region termed the "growth zone." Prior experimental and theoretical research indicates that elongation growth rate of the stage IVb sporangiophore can be regulated by controlling the cell wall mechanical properties within the growth zone and the magnitude of the turgor pressure. A quantitative biophysical model for elongation growth rate is required to elucidate the relationship between wall mechanical properties and turgor pressure during growth regulation. In this study, it is hypothesized that the mechanical properties of the wall within the growth zone of stiff mutant sporangiophores are different compared to wild type (WT). A biophysical equation for elongation growth rate is derived for fungal and plant cells with a growth zone. Two strains of stiff mutants are studied, C149 madD120 (-) and C216 geo- (-). Experimental results demonstrate that turgor pressure is larger but irreversible wall deformation rates within the growth zone and growth zone length are smaller for stiff mutant sporangiophores compared to WT. These findings can explain the diminished tropic responses of the stiff mutant sporangiophores. It is speculated that the defective genes affect the amount of wall-building material delivered to the inner cell wall.