Vibrational Frequencies Research Articles

Failure law of hydraulic pipe joints sealing performance under vibration loads

Aviation hydraulic pipe joints are inevitably affected by vibration loads during service. Fatigue relaxation occurs in the pipe joint structure by vibration, and fretting fatigue wear occurs in its sealing interface, leading to a decline in sealing performance. In order to investigate the sealing performance of hydraulic pipe joints affected by vibration load, this paper first analyzes the modal distribution of the sealing system pipeline under different hydraulic pressures and hydraulic fluid flow rates through vibration frequency sweeping experiments. Secondly, the vibration load is applied to the pipe joints for different numbers of cycles, which reveals the microscopic wear behavior of the sealing interfaces under different tightening torques. Finally, by carrying out the leakage measurement experiment under vibration load, the evolution law of the sealing performance of pipe joints under different hydraulic fluid pressures and tightening torques was obtained.

Integrating low-cost GNSS and MEMS accelerometer for precise dynamic displacement monitoring

We assess the performance of the self-developed receiver coupling dual-frequency low-cost GNSS chipset and IMU MEMS sensor. The system also comprises software dedicated to vibration monitoring based on relative kinematic positioning in a post-processing mode. The observation assessment reveals high accuracy of low-cost GNSS and MEMS accelerometer data. The Septentrio Mosaic X5 chipset exhibits competitive to high-grade receivers’ phase observation noise, outperformance in code noise level and observation auto-correlation at a level that may be neglected even in high-rate applications. The evaluation of the MEMS accelerometer data proves that the sensor accuracy is adequate for vibration monitoring. With the shake table experiment, we examine the performance of vibration recovery. An advantage of the coupled solution over a GNSS-only one is documented with a 15 % reduction of the amplitude error. The backward smoothing of coupled solutions drives the next 20 % error drop. Finally, the high performance of the coupled solution based on low-cost GNSS & accelerometer is confirmed by a mean amplitude error of 0.4 mm. The frequency analyses indicate that both coupled and single-sensor solutions precisely detect the vibration frequencies; however, they also confirm the outperformance of the former over the latter. The power spectra of the recovered displacement time series accentuate the benefits of GNSS + accelerometer fusion and backward filtering for reducing displacement noise.

Solvent Effect on Dative and Ionic Bond Strengths: A Unified Theory from Potential Analysis and Valence-Bond Computations.

Solvent molecules interact with a solute through various intermolecular forces. Here we employed a potential energy surface (PES) analysis to interpret the solvent-induced variations in the strengths of dative (Me3NBH3) and ionic (LiCl) bonds, which possess both ionic and covalent (neutral) characteristics. The change of a bond is driven by the gradient (force) of the solvent-solute interaction energy with respect to the focused bond length. Positive force shortens the bond length and increases the bond force constant, leading to a blue-shift of the bond stretching vibrational frequency upon solvation. Conversely, negative force elongates the bond, resulting in a reduced bond force constant and red-shift of the stretching vibrational frequency. The different responses of Me3NBH3 and LiCl to solvation are studied with valence bond (VB) theory, as Me3NBH3 and LiCl are dominated by the neutral covalent VB structure and the ionic VB structure, respectively. The dipole moment of an ionic VB structure increases along the increasing bond distance, while the dipole moment of a neutral covalent VB structure increases with the decreasing bond distance. The roles of the dominating VB structures are further examined by the geometry optimizations and frequency calculations with the block-localized wavefunction (BLW) method.

Experimental, quantum chemical spectroscopic investigation, topological, molecular docking/dynamics and biological assessment studies of 2,6-Dihydroxy-4-methyl quinoline

The present work is a comprehensive investigation of the spectral, electronic structure, bonding, and reactivity of the 2,6-dihydroxy-4-methylquinoline (26DH4MQ) molecule through a wide range of experimental and quantum chemical spectroscopic calculations techniques, along with its applications as nonlinear optical materials and biological assessments. The study utilized density functional theory (DFT) and time-dependent density functional theory (TD-DFT) with the B3LYP method and the 6-311G++(d,p) basis set to analyze the structural and molecular properties of 26DH4MQ. The findings from UV–Vis, FT-IR, and FT-NMR spectroscopy show a strong agreement between the experimentally obtained vibrational frequencies and chemical shifts and those predicted by computational methods. Local reactivity descriptors, such as the dual descriptor, Fukui functions, and the molecular electrostatic potential (MEP) map, were used to identify the reactive regions of the molecule. Additionally, natural bond orbital (NBO) analysis provided insights into the charge transfer characteristics of 26DH4MQ, which helps to stabilize the molecular system. The study also revealed notable nonlinear optical (NLO) properties, with polarizability (18.52 × 10–24e.s.u.) and first-order hyperpolarizability (2.26 × 10–30e.s.u.) values that surpass those of standard organic compounds, suggesting significant potential for optoelectronic applications. The biological evaluation of 26DH4MQ assessed its drug-likeness, toxicity, enzyme inhibition, and ADME (Absorption, Distribution, Metabolism, and Excretion) parameters, highlighting its pharmaceutical potential. Furthermore, molecular docking and dynamics studies illustrated the compound's interaction with proteins, indicating its potential role as an insulin inhibitor.

Effects of ultrasonic vibration on residual stress distribution and local mechanical properties of AA6061/Ti6Al4V dissimilar joints by resistance spot welding

The joining of dissimilar titanium and aluminum alloys has potential applications in railway and aerospace industries, owing to substantial weight reduction and better economic viability. In this study, the residual stress distribution and local mechanical performance of ultrasonic-assisted resistance spot welding (UaRSW) welds were investigated. The welding current, welding time, and electrode force of the RSW process were set as 9.0 kA, 350 ms, and 1.0 kN respectively, and the frequency and power of ultrasonic vibration were 20 kHz and 800 W. The residual stress was evaluated by X-ray diffraction (XRD) method and numerical simulation, and these methods showed a reasonable match. There was tensile residual stress distributed on RSW welds and UaRSW welds, but the value of residual stress was reduced by about 30% at welding nugget and 20% at heat affected zone (HAZ) with the ultrasonic vibration, the reduction of residual stress in UaRSW welds was attributed to the more uniform temperature distribution and lower plastic deformation resistant of AA6061. The welding peak temperature was decreased from 1673.4 °C to 1584.2 °C with the ultrasonic vibration, resulted from the modified Al/Ti contact surface and reduced contact resistance. The miniature tensile test results showed the improvement of mechanical performance by ultrasonic vibration. The maximum load of welding nugget region increased from 19.6 N to 22.3 N, and the elongation obtained 10% increase. This hybrid welding technique shows a potential to improve the quality of welds with ensured efficiency, which is also simple to realize automation in the manufacturing industry.

Investigating the antioxidant potential and mechanism of a hydrazide bioactive component of garlic: insights from density functional theory calculations, drug-likeness and molecular docking studies.

Glutathione remains one of the most efficient antioxidant compounds in living systems, and the biological abilities of hydrazides have been well documented in literature. This study highlights the phytochemical constituents of garlic and the separation of the bioactive benzoic acid, 4-chloro- 1-(4-methoxyphenyl) hydrazide (BA4C) using gas chromatography-mass spectroscopy (GC-MS) technique. Preliminary phytochemical screening reveals the presence of alkaloids, saponins, flavonoids, tannins, terpenoids, steroids and phenols. Computationally, compound BA4C was optimized using the B3LYP/aug-cc-PVDZ DFT method. Spectroscopic studies of the compound involved analysis of the vibrational FT-IR frequencies and the modes of vibrations. Frontier molecular orbitals analysis records an energy gap of 4.3391eV; NBO studies reveal that the compound has strong perturbation energies of 246kcal/mol and 269kcal/mol among its intramolecular interactions such as *C12 - C13 to *C14 - C15 and *C11 - C16 to *C14 - C15, respectively. According to the visualization of non-covalent interactions, steric repulsions were observed at the core of the phenyl and benzene rings. However, other regions of the compound depict a significant balance of forces between steric repulsions and van der Waals forces. To significantly deduce the reducing power of compound BA4C, electrons were found to be highly localized at the methoxy and hydrazide moieties significantly implying their propensity to donate electrons to oxidized systems. Furthermore, ADMET analysis reveals that the compound has two hydrogen donors. Most significantly, the compound binds to NADPH dehydrogenase (5V4P) and glutathione reductase (1XAN) with binding energies of - 6.0kcal/mol and - 8.0kcal/mol showing considerable favourable binding feasibility as well as forming plural hydrogen bonds with the amino acid residues. Notably, BA4C was bonded at the active site of 1XAN, which implies the ability of the compound for the reduction of oxidized glutathione.

Comparative study of CO adsorption on Au, Cu, MoO2 and MoS2 2D Nanoparticles

This study focuses on a comparative analysis of the electronic properties of triangular, irregular hexagonal, and octagonal 2D nanoparticles containing 10, 12, and 14 motifs, made of Au, Cu, MoO2, and MoS2. The investigation was carried out using density functional theory. The formation energies and vibrational frequencies demonstrate that the 2D nanostructure configurations can exist as stable structures. Edge atoms with lower coordination numbers than central atoms, are the preferred sites for CO adsorption. Using orbital-weighting dual descriptors calculated from Fukui functions enabled the identification of a majority nucleophilic attack sites in Au and Cu nanoparticles, while MoO2 and MoS2-based nanoparticles present almost as many electrophilic sites as nucleophilic sites. The charge transferred between the nanostructures and the CO molecule and the redistribution of the projected density of states were used to assess the strength of interfacial bonds and the nature of the fundamental interaction involved in the bonding.

Integrated design method for protection against vibration of offshore platform plate structure

The paper integrates the modal avoidance method, pedestal design method, and dynamic vibration absorber theory to investigate vibration control technology for offshore platform plate structures. We develop an integrated design method for vibration suppression by controlling the vibration excitation load, vibration transmission, and vibration energy dissipation. Firstly, a modal avoidance design is implemented to suppress vibration transmission along the propagation path of the plate structure. Subsequently, pedestal optimization is conducted for pedestal structure to attenuate vibration excitation at the input end. Finally, dynamic vibration absorber theory is employed to control dominant vibration frequency responses further and achieve multi-target vibration control. Case simulation results demonstrate that the integrated design method reduces the acceleration vibrations level at 113.75, 145.61, and 153 Hz, and this method could guide multi-objective vibration control in offshore platform plate structures.

Computational study of the supramolecular complexation of azocompounds with cucurbit[7]uril: effects on the production and release of free radicals.

An inclusion complex between 2,2'-azobis(2-methylpropionamidine) dihydrochloride (AAPH), a widely employed azocompound, and cucurbit[7]util (CB[7]), has shown an increased yield of radicals derived from the homolytic cleavage of the azo bond. Aimed to get insights about the formation of complexes and their effect on the yield of radicals production, complexes of CB[7] with seven azocompounds were studied by computational methods. Molecular electrostatic surfaces and structural analysis showed that the inclusion of symmetrical azocompounds inside of CB[7] depends mainly on the charge density and position of the functional groups at the main chain of the azoderivative. Analysis of non-covalent interactions and thermodynamic outcomes revealed that positively charged azocompounds with amidinium or imidazolium groups presented strong favorable interactions (multiple hydrogen bonds) with the oxygens of CB[7] portals. Additionally, carbon-centered radicals generated from the complexes (azocompounds@CB[7]) were corroborated using the electron localization function (ELF). Results evidenced that the strength of the interactions and the level of inclusion (partial or complete) between the azocompound and CB[7] determined the final orientation of the radicals (located out- or inside of the CB[7] cavity). Obtained results could be employed to design new supramolecular systems based on the properties of azocomplound@CB[7] complexes for new scientific or industrial applications. First-principles calculations at B3LYP-D3BJ/6-311g(d,p) level theory in the gas phase and in solvent (PCM, water) were performed in Gaussian 16 software package. The dispersion energy correction was included through the Grimme's dispersion with Becke-Johnson damping D3(BJ). Thermodynamical data and the minimum character of all structures were obtained from vibrational frequency calculations. NBO, Multiwfn, Chemcraft, and NCIPLOT software were used to perform population analysis, analyze outcomes, visualize data, and display non-covalent interactions respectively.

Probing the Electric Field Response of a Water Molecule Confined in Small Carbon Nanocages: A Density Functional Theory Investigation.

We consider a water molecule under tight confinement in the small-sized fullerenes (C28, C30, C32) within the density functional theory (DFT) calculations with suitable exchange-correlation functionals. Such nanoscopic molecular cages provide an ideal setup to study their characteristic properties not present in the condensed phase. The water molecule entirely loses its feature of typical water when it is confined in small fullerenes of size equal to C30or smaller, in which the asymmetric O-H stretching vibration occurs at a lower wavenumber than the symmetric stretching. We study the response of the confined water molecule to the applied electric fields in terms of change in geometrical parameters, NMR spin-spin coupling constants, dipole moment, HOMO-LUMO (HL) gap, and vibrational frequency shift. The electric field shielding property of small-sized fullerene cages is explored and found to be strongly correlated with the HL gap. Since the electric field modulates the gap to decrease generally, shielding efficiency varies with field strength, thereby making large fields better shielded than small fields for the small penetration factor at large fields. The results that hold significance for technological applications are discussed.

Analyzing cyclobutane: A vibrational hamiltonian approach using dynamical U(2) Lie Algebras

This study uses a one-dimensional Lie algebraic framework, precisely adapted to the symmetry of molecules, to investigate the vibrational frequencies of cyclobutane. A vibrational Hamiltonian is also constructed using one-dimensional Morse oscillators, preserving the D2d point group symmetry for each molecule. The analysis compares the calculated fundamental vibrational frequencies with the observed experimental frequencies, resulting in a root mean square deviation of 0.886 cm-1. The result highlights the exceptional precision of the U(2) Lie algebraic Hamiltonian in accurately predicting the vibrational frequencies and their combination bands at the sub-cm-1 level of precision. Specifically, this computational approach has the potential to achieve these results with lower computational costs compared to traditional theoretical approaches. The broader implications of our study suggest that the U(2) Lie algebraic framework can be effectively applied to a wide range of molecular systems, offering significant advantages in fields such as material science, drug design, and environmental monitoring by providing precise and efficient vibrational spectral analyses. KEY WORDS: Vibrational Hamiltonian, Vibrational frequencies, Morse oscillator, Cyclobutane, Lie algebraic method Bull. Chem. Soc. Ethiop. 2024, 38(6), 1887-1896. DOI: https://dx.doi.org/10.4314/bcse.v38i6.29

Synthesis, crystal structure, spectroscopic, electronic and vibrational properties of N′-[(E)-3-pyridinylmethylene]nicotinohydrazide trihydrate: Experimental and computational study

N′-[(E)-3-pyridinylmethylene]nicotinohydrazide trihydrate (C12H10N4O·3(H2O)) was synthesized and its structure was determined by single crystal X-ray diffraction method. X-ray analysis showed that the compound crystalized in the triclinic system P-1 with a = 7.1134 (3) Å, b = 10.0208 (4) Å, c = 10.3601 (4) Å, α = 96.386 (3)°, β = 96.995 (3)°, γ = 101.219 (4)°, V = 712.05 (5) Å3 and Z = 2 and exhibits that the title compound (I) consists of N′-[(E)-3-pyridinylmethylene]nicotinohydrazide (II) (C12H10N4O), and three water molecules of crystallization. The two water molecules are attached to the third water molecule through intermolecular two OH…O hydrogen bonds. At the same time, this water molecule is linked to the NH amide group of the hydrazone by an intermolecular NH…O hydrogen bond. Hirshfeld surface (HS) analyses were carried out are to visualise the intermolecular interactions in the crystals of Compound I. The geometric optimization of the titled compound has been carried out by different computational methods such as by Hatree Fock (HF) and Density Functional Theory (DFT) methods with the 6–311++G (d,p) basis set. The vibrational frequency, dipole moment (μ), polarizability (α), hyperpolarizability (β), and electronic properties including the highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO–LUMO) of the compound have been calculated at the level of both theories. In the results of crystal analysis and geometry calculations of the compound I, it was observed that intermolecular hydrogen bonds, N2H2A…O3, O3H31…O2 and O3H32…O4, were formed. The energy band gap (Eg = ELUMO-EHOMO) values were also obtained by using ELUMO and EHOMO at the level of both theories. The value of equilibrium (ground state) dipole moment of the studied molecule was calculated to be 8.31 Debye in B3LYP and 7.55 Debye in HF. The calculated hyperpolarizability values at the B3LYP/6–311++G(d,p) of the compound are 2.53 × 10−30 esu and this value corresponds to 6.79 times the hyperpolarizability value of urea.

Selective incorporation of antimony into gallium nitride

Dilute concentrations of antimony (Sb) incorporation into GaN induce strong bandgap bowing and tunable room-temperature photoluminescence from the UV to the green spectral regions. However, the atomistic details of the incorporation of Sb into the GaN host remain unclear. In this work, we use first-principles calculations to understand the thermodynamics of Sb substitution into GaN and its effect on the optical and Raman spectra. Although it is empirically considered that Sb is preferentially incorporated as an anion (Sb3−) into the N sublattice, we demonstrate that Sb can also be incorporated as a cation (Sb3+, Sb5+) into the metal sublattice. Our thermodynamic analysis demonstrates that SbN0, SbGa2+, and SbGa0 can co-exist under Ga-rich conditions in n-type samples. We further confirm the dual incorporation of Sb by calculating the vibrational frequencies of different anionic and cationic substitutions to explain the origins of experimentally observed additional Raman peaks of Sb-doped GaN. Moreover, the calculated band structures of different Sb substitutions into GaN explain the experimental photoluminescence and optical absorption spectra. Overall, our analysis suggests that the coexistence of Sb3−, Sb3+, and Sb5+ substitutions into GaN explains the totality of experimental measurements. Our results demonstrate that the selective incorporation of Sb into GaN (and potentially other group-V elements such as As, P, or Bi) by tuning the growth conditions can drastically modify the electronic properties, for applications in visible light emitters and photocatalysis.

Rapid wideband characterization of viscoelastic material properties by Bessel function-based time harmonic ultrasound elastography (B-THE)

Elastography is an emerging diagnostic technique that uses conventional imaging modalities such as sonography or magnetic resonance imaging to quantify tissue stiffness. However, different elastography methods provide different stiffness values, which require calibration using well-characterized phantoms or tissue samples. A comprehensive, fast, and cost-effective elastography technique for phantoms or tissue samples is still lacking.Therefore, we propose ultrasound Bessel-fit-based time harmonic elastography (B-THE) as a novel tool to provide rapid feedback on stiffness-related shear wave speed (SWS) and viscosity-related wave penetration rate (PR) over a wide range of harmonic vibration frequencies. The method relies on external induction and B-mode capture of cylindrical shear waves that satisfy the Bessel wave equation for efficient fit-based parameter recovery. B-THE was demonstrated in polyacrylamide phantoms in the frequency range of 20–200 Hz and was cross-validated by magnetic resonance elastography (MRE) using clinical 3-T MRI and compact 0.5-T tabletop MRI scanners. Frequency-independent material parameters were derived from rheological models and validated by numerical simulations.B-THE quantified frequency-resolved SWS and PR 13 to 176 times faster than more expensive clinical MRE and tabletop MRE and have a good accuracy (relative deviation to reference: 6 %, 10 % and 4 % respectively). Simulations of liver-mimicking material phantoms showed that a simultaneous fit of SWS and PR based on the fractional Maxwell rheological model outperformed a fit on PR solely.B-THE provides a comprehensive and fast elastography technique for the quantitative characterization of the viscoelastic behavior of soft tissue mimicking materials.

Influences of ultrasonic vibration directions, amplitudes, and frequencies on sapphire polishing studied by molecular dynamics

The sapphire surface morphology, atom removal rate, temperature, polishing force, subsurface damage, dislocation, and stress were explored under different ultrasonic directions, frequencies and amplitudes through molecular dynamics (MD). For both vertical and horizontal vibration, the rising ultrasonic frequency and amplitude will reduce the tangential and normal force, and increase the subsurface temperature and the material removal rate (MRR). Higher frequencies promote the basal dislocation, thus reducing the subsurface damage. Higher amplitudes cause thinner subsurface damage layer under horizontal vibration. However, it is opposite at vertical vibration. The horizontal vibration can obtain a flatter polished surface and a thinner subsurface damage layer due to the longer trajectory and less impact on sapphire surface. This study can provide reference for sapphire high-quality polishing.

Research on screening effect and time-frequency characteristics of screen surface with additional striking beam

ABSTRACT In this study, a new flexible screen surface structure with an additional striking beam was proposed for improved efficiency and addressing the clogging issue while processing moist coal material. Vibration tests were used to analyze the time-frequency characteristics of the screen surface and the striking beam under no-load and load conditions. The effects of different process parameters on the elastic screening effect of viscous and wet materials were explored. Further, the industrial application of the equipment was preliminarily carried out. The results showed that the load did not affect the main vibration frequency of the elastic screen surface and the striking beam. When the axis distance was adjusted to 7.5 cm, the displacement from the feeding end to the discharge end gradually decreased, promoting the rapid loosening and stratification of the material group. Semi-industrial tests showed that the optimal screening effects had a screening efficiency of 92.16% and a total misplaced content of 5.95% when exciting force was 18 kN, the exciting frequency was 10.8 Hz, the feeding rate was 9.36 t/h, the distance was 7.5 cm, and the moisture content was 8.21%. The GQPSS1848 vibrating screen applied in the industry achieved a screening efficiency of 86.66% at a processing capacity of 85 t/h with a broad commercial prospect. The study aims to provide theoretical and technical support for the research and development of flexible screening equipment and the efficient classification of −3 mm sticky and wet materials.

Vibrational Frequencies of Tetrachloroethylene using Lie Algebraic Framework

This study employs a sophisticated computational approach to predict tetrachloroethylene's higher overtone vibrational frequencies (C2Cl4) up to the fourth overtone. We utilize a Lie algebraic framework within the context of the vibrational Hamiltonian. The method involves replacing tetrachloroethylene's carbon-chlorine (C-Cl) bonds with unitary Lie algebras. The resulting Hamiltonian is written in terms of Casimir and Majorana's invariant operators and parameters. The derived Hamiltonian operator effectively characterizes the stretching vibrations inherent to the molecular structure. This approach enhances our understanding of the vibrational dynamics of tetrachloroethylene at higher overtones, offering valuable insights for applications in diverse scientific and technological fields.

The Influence of Vibration Frequency and Vibration Duration on the Mechanical Properties of Zhanjiang Formation Structural Clay

The Influence of Vibration Frequency and Vibration Duration on the Mechanical Properties of Zhanjiang Formation Structural Clay

Modulating Wetting States of Molten Aluminum Droplets on SiO2 Surfaces via Vertical Sinusoidal Vibrations.

Vibration affects the wetting behavior of droplets, and it is feasible to use vibration to modulate the adhesion characteristics of droplets. In this paper, the effect of vertical sinusoidal vibrations on the wettability of molten aluminum droplets on the substrate surfaces of smooth and with nanopillars is investigated. The increase in the frequency or amplitude of the vibration leads to a rise in the interfacial potential energy between the molten droplets and the substrate, which in turn leads to the occurrence of the Wenzel-Cassie transition. Once the vibration frequency reaches the threshold values, the molten droplets leave from the substrate, that is, dewetting occurs. The molten droplets in the Wenzel state undergo a Wenzel-Cassie transition before dewetting occurs. A phase diagram describing the frequency thresholds at which the molten aluminum droplets undergo dewetting and the Wenzel-Cassie transition at different amplitudes is plotted. For a specific amplitude, the frequency of vibration required for dewetting to occur in molten aluminum droplets in the Young state is lower than that in the Wenzel state. The needed vibrational frequency for dewetting or the Wenzel-Cassie transition decreases with increasing amplitude.

Two-dimensional graphyne monolayers as substrate discs of piezoelectric nanogenerators: A hybrid atomistic-continuum model study

The different phases of α-, β-, and γ-graphyne, which are new types of two-dimensional carbon allotropes, hold promise as potential candidates for designing substrate discs in piezoelectric nanogenerators. Accurate modeling of the bending rigidity and stretching properties as well as resonance frequencies of these materials is crucial for engineering applications like nano-resonator and nanogenerator systems. This step is imperative in designing and advancing future applications involving these structures. This study aims to create a hybrid atomistic-continuum model for modeling graphyne monolayers used as substrate discs in nanogenerators. The model integrates the benefits of both atomistic and continuum approaches. Based on the results, α-graphyne is the least mechanically stable, while γ-graphyne is the most stable. However, in terms of vibration frequency, α-graphyne has the highest frequency while γ-graphyne has the lowest. Therefore, β-graphyne, with moderate stability and resonance frequency, is recommended as the ideal choice for the substrate disc in piezoelectric nanogenerators. It can function within the Q-F frequency range (30–140 GHz) and induce deformation in the piezoelectric shim as well as generation voltage.