20 research outputs found
ΠΠΎΠ΄Π΅Π»ΠΈΡΠΎΠ²Π°Π½ΠΈΠ΅ ΠΏΠΎΠΌΠ΅Ρ ΠΎΠ·Π°ΡΠΈΡΠ΅Π½Π½ΡΡ ΡΠ΅ΡΠ΅Π²ΡΡ ΠΊΠ°Π½Π°Π»ΠΎΠ² Π΄Π»Ρ ΡΠ΅Ρ Π½ΠΈΡΠ΅ΡΠΊΠΈΡ ΡΠΈΡΡΠ΅ΠΌ ΡΠΏΡΠ°Π²Π»Π΅Π½ΠΈΡ
The paper focuses on the application of digital adaptive filtering to ensure the noise-free speech channels of control systems. Noise is an extraneous signal, which enters the channel device input together with the speech. The article conducts a comparative analysis of the three adaptation algorithms (LMS, NLMS, RLS) to be useful for noise suppression. At the same time, an adaptive suppression mechanism with two microphones on the speech channel is used.The related publications compared the algorithms by one or two criteria. This paper offers three comparison criteria: computational complexity, quality of noise suppression, and rate of convergence to the steady-state condition. The number of vector operations in algorithm procedures estimates temporary computational complexity.To compare algorithms by the other two criteria, their implementation was simulated in MATLAB. As the noise, were used the white and pink noise, a sine wave, and a model of the non-stationary signal as well. The noise suppression coefficient and the number of iterations before transition to the steady-state condition have been obtained. The algorithm RLS showed the best quality of suppression while the NLMS algorithm revealed the highest rate of convergence. Experiments have shown that the white noise is suppressed worse, but faster than the sine one.The paper explores influence of some factors on the process of adaptation. It is shown that increase in filter dimension leads to improving quality of adaptation and its speed-down. From simulation results it follows that the noise suppression coefficient has the highest values when at the filter input there are approximately equal signal and noise powers.The results allow us to make commendation to use the NLMS algorithm for real-time systems, and the RLS one for technical systems aimed at recordings of speech signals. The above algorithms can be successfully implemented on modern technology platforms, comprising high-performance digital signal processors and associated peripherals.Π‘ΡΠ°ΡΡΡ ΠΏΠΎΡΠ²ΡΡΠ΅Π½Π° ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡ ΡΠΈΡΡΠΎΠ²ΠΎΠΉ Π°Π΄Π°ΠΏΡΠΈΠ²Π½ΠΎΠΉ ΡΠΈΠ»ΡΡΡΠ°ΡΠΈΠΈ Π΄Π»Ρ ΠΎΠ±Π΅ΡΠΏΠ΅ΡΠ΅Π½ΠΈΡ ΠΏΠΎΠΌΠ΅Ρ
ΠΎΠ·Π°ΡΠΈΡΠ΅Π½Π½ΠΎΡΡΠΈ ΡΠ΅ΡΠ΅Π²ΡΡ
ΠΊΠ°Π½Π°Π»ΠΎΠ² ΡΠΈΡΡΠ΅ΠΌ ΡΠΏΡΠ°Π²Π»Π΅Π½ΠΈΡ, ΠΏΠΎΠ½ΠΈΠΌΠ°Ρ ΠΏΠΎΠ΄ ΠΏΠΎΠΌΠ΅Ρ
ΠΎΠΉ ΠΏΠΎΡΡΠΎΡΠΎΠ½Π½ΠΈΠΉ ΡΠΈΠ³Π½Π°Π», ΠΏΠΎΠΏΠ°Π΄Π°ΡΡΠΈΠΉ Π²ΠΌΠ΅ΡΡΠ΅ Ρ ΡΠ΅ΡΡΡ Π½Π° Π²Ρ
ΠΎΠ΄ ΠΊΠ°Π½Π°Π»ΡΠ½ΠΎΠ³ΠΎ ΡΡΡΡΠΎΠΉΡΡΠ²Π°. Π ΡΠ°Π±ΠΎΡΠ΅ ΠΏΡΠΎΠ²Π΅Π΄Π΅Π½ ΡΡΠ°Π²Π½ΠΈΡΠ΅Π»ΡΠ½ΡΠΉ Π°Π½Π°Π»ΠΈΠ· ΡΡΠ΅Ρ
Π°Π»Π³ΠΎΡΠΈΡΠΌΠΎΠ² Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠΈ (LMS, NLMS, RLS), ΠΏΡΠΈΠΌΠ΅Π½ΠΈΠΌΡΡ
Π΄Π»Ρ ΠΏΠΎΠ΄Π°Π²Π»Π΅Π½ΠΈΡ ΠΏΠΎΠΌΠ΅Ρ
. ΠΡΠΈ ΡΡΠΎΠΌ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ ΠΌΠ΅Ρ
Π°Π½ΠΈΠ·ΠΌ Π°Π΄Π°ΠΏΡΠΈΠ²Π½ΠΎΠ³ΠΎ ΠΏΠΎΠ΄Π°Π²Π»Π΅Π½ΠΈΡ Ρ Π΄Π²ΡΠΌΡ ΠΌΠΈΠΊΡΠΎΡΠΎΠ½Π°ΠΌΠΈ Π² ΡΠ΅ΡΠ΅Π²ΠΎΠΌ ΠΊΠ°Π½Π°Π»Π΅.Π Π±Π»ΠΈΠ·ΠΊΠΈΡ
ΠΏΠΎ ΡΠ΅ΠΌΠ΅ ΠΏΡΠ±Π»ΠΈΠΊΠ°ΡΠΈΡΡ
ΡΡΠ°Π²Π½Π΅Π½ΠΈΠ΅ Π°Π»Π³ΠΎΡΠΈΡΠΌΠΎΠ² ΠΏΡΠΎΠ²ΠΎΠ΄ΠΈΠ»ΠΎΡΡ ΠΏΠΎ ΠΎΠ΄Π½ΠΎΠΌΡ ΠΈΠ»ΠΈ Π΄Π²ΡΠΌ ΠΊΡΠΈΡΠ΅ΡΠΈΡΠΌ. Π Π΄Π°Π½Π½ΠΎΠΉ ΡΠ°Π±ΠΎΡΠ΅ Π²ΡΠ±ΡΠ°Π½Ρ ΡΡΠΈ ΠΊΡΠΈΡΠ΅ΡΠΈΡ ΡΡΠ°Π²Π½Π΅Π½ΠΈΡ: Π²ΡΡΠΈΡΠ»ΠΈΡΠ΅Π»ΡΠ½Π°Ρ ΡΠ»ΠΎΠΆΠ½ΠΎΡΡΡ, ΠΊΠ°ΡΠ΅ΡΡΠ²ΠΎ ΠΏΠΎΠ΄Π°Π²Π»Π΅Π½ΠΈΡ ΠΏΠΎΠΌΠ΅Ρ
ΠΈ ΠΈ ΡΠΊΠΎΡΠΎΡΡΡ ΡΡ
ΠΎΠ΄ΠΈΠΌΠΎΡΡΠΈ ΠΊ ΡΡΡΠ°Π½ΠΎΠ²ΠΈΠ²ΡΠ΅ΠΌΡΡΡ ΡΠ΅ΠΆΠΈΠΌΡ. ΠΡΠ΅ΠΌΠ΅Π½Π½Π°Ρ Π²ΡΡΠΈΡΠ»ΠΈΡΠ΅Π»ΡΠ½Π°Ρ ΡΠ»ΠΎΠΆΠ½ΠΎΡΡΡ ΠΎΡΠ΅Π½Π΅Π½Π° ΠΏΠΎ ΠΊΠΎΠ»ΠΈΡΠ΅ΡΡΠ²Ρ Π²Π΅ΠΊΡΠΎΡΠ½ΡΡ
ΠΎΠΏΠ΅ΡΠ°ΡΠΈΠΉ Π² ΠΏΡΠΎΡΠ΅Π΄ΡΡΠ°Ρ
Π°Π»Π³ΠΎΡΠΈΡΠΌΠΎΠ².ΠΠ»Ρ ΡΡΠ°Π²Π½Π΅Π½ΠΈΡ Π°Π»Π³ΠΎΡΠΈΡΠΌΠΎΠ² ΠΏΠΎ Π΄Π²ΡΠΌ Π΄ΡΡΠ³ΠΈΠΌ ΠΊΡΠΈΡΠ΅ΡΠΈΡΠΌ Π±ΡΠ»ΠΎ ΠΏΡΠΎΠ²Π΅Π΄Π΅Π½ΠΎ ΠΌΠΎΠ΄Π΅Π»ΠΈΡΠΎΠ²Π°Π½ΠΈΠ΅ ΠΈΡ
ΡΠ°Π±ΠΎΡΡ Π² ΡΡΠ΅Π΄Π΅ MATLAB. Π ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ ΠΏΠΎΠΌΠ΅Ρ
ΠΈ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½Ρ Π±Π΅Π»ΡΠΉ ΠΈ ΡΠΎΠ·ΠΎΠ²ΡΠΉ ΡΡΠΌΡ, ΡΠΈΠ½ΡΡΠΎΠΈΠ΄Π°Π»ΡΠ½ΡΠΉ ΡΠΈΠ³Π½Π°Π», Π° ΡΠ°ΠΊΠΆΠ΅ ΠΌΠΎΠ΄Π΅Π»Ρ Π½Π΅ΡΡΠ°ΡΠΈΠΎΠ½Π°ΡΠ½ΠΎΠ³ΠΎ ΡΠΈΠ³Π½Π°Π»Π°. ΠΠΎΠ»ΡΡΠ΅Π½Ρ ΠΊΠΎΡΡΡΠΈΡΠΈΠ΅Π½Ρ ΠΏΠΎΠ΄Π°Π²Π»Π΅Π½ΠΈΡ ΠΏΠΎΠΌΠ΅Ρ
ΠΈ ΠΈ ΡΠΈΡΠ»ΠΎ ΠΈΡΠ΅ΡΠ°ΡΠΈΠΉ Π°Π»Π³ΠΎΡΠΈΡΠΌΠ° Π΄ΠΎ ΠΏΠ΅ΡΠ΅Ρ
ΠΎΠ΄Π° Π² ΡΡΡΠ°Π½ΠΎΠ²ΠΈΠ²ΡΠΈΠΉΡΡ ΡΠ΅ΠΆΠΈΠΌ. ΠΠ°ΠΈΠ»ΡΡΡΠ΅Π΅ ΠΊΠ°ΡΠ΅ΡΡΠ²ΠΎ ΠΏΠΎΠ΄Π°Π²Π»Π΅Π½ΠΈΡ ΠΏΠΎΠΊΠ°Π·Π°Π» Π°Π»Π³ΠΎΡΠΈΡΠΌ RLS, Π½Π°ΠΈΠ²ΡΡΡΡΡ ΡΠΊΠΎΡΠΎΡΡΡ ΡΡ
ΠΎΠ΄ΠΈΠΌΠΎΡΡΠΈ β Π°Π»Π³ΠΎΡΠΈΡΠΌ NLMS. ΠΠΏΡΡΡ ΠΏΠΎΠΊΠ°Π·Π°Π»ΠΈ, ΡΡΠΎ Π±Π΅Π»ΡΠΉ ΡΡΠΌ ΠΏΠΎΠ΄Π°Π²Π»ΡΠ΅ΡΡΡ Ρ
ΡΠΆΠ΅, Π½ΠΎ Π±ΡΡΡΡΠ΅Π΅, ΡΠ΅ΠΌ ΡΠΈΠ½ΡΡΠΎΠΈΠ΄Π°Π»ΡΠ½Π°Ρ ΠΏΠΎΠΌΠ΅Ρ
Π°.ΠΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΎ Π²Π»ΠΈΡΠ½ΠΈΠ΅ ΡΡΠ΄Π° ΡΠ°ΠΊΡΠΎΡΠΎΠ² Π½Π° ΠΏΡΠΎΡΠ΅ΡΡ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠΈ. ΠΠΎΠΊΠ°Π·Π°Π½ΠΎ, ΡΡΠΎ ΡΠ²Π΅Π»ΠΈΡΠ΅Π½ΠΈΠ΅ ΡΠ°Π·ΠΌΠ΅ΡΠ½ΠΎΡΡΠΈ ΡΠΈΠ»ΡΡΡΠ° Π²Π΅Π΄Π΅Ρ ΠΊ ΠΏΠΎΠ²ΡΡΠ΅Π½ΠΈΡ ΠΊΠ°ΡΠ΅ΡΡΠ²Π° Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠΈ ΠΈ ΡΠ½ΠΈΠΆΠ΅Π½ΠΈΡ Π΅Π΅ ΡΠΊΠΎΡΠΎΡΡΠΈ. ΠΠ· ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΠΎΠ² ΠΌΠΎΠ΄Π΅Π»ΠΈΡΠΎΠ²Π°Π½ΠΈΡ ΡΠ»Π΅Π΄ΡΠ΅Ρ, ΡΡΠΎ ΠΊΠΎΡΡΡΠΈΡΠΈΠ΅Π½Ρ ΠΏΠΎΠ΄Π°Π²Π»Π΅Π½ΠΈΡ ΠΏΠΎΠΌΠ΅Ρ
ΠΏΡΠΈΠ½ΠΈΠΌΠ°Π΅Ρ Π½Π°ΠΈΠ±ΠΎΠ»ΡΡΠΈΠ΅ Π·Π½Π°ΡΠ΅Π½ΠΈΡ, Π΅ΡΠ»ΠΈ ΠΌΠΎΡΠ½ΠΎΡΡΠΈ ΡΠΈΠ³Π½Π°Π»Π° ΠΈ ΠΏΠΎΠΌΠ΅Ρ
ΠΈ Π½Π° Π²Ρ
ΠΎΠ΄Π΅ ΡΠΈΠ»ΡΡΡΠ° ΠΏΡΠΈΠΌΠ΅ΡΠ½ΠΎ ΠΎΠ΄ΠΈΠ½Π°ΠΊΠΎΠ²Ρ.Π Π΅Π·ΡΠ»ΡΡΠ°ΡΡ ΠΏΠΎΠ·Π²ΠΎΠ»ΡΡΡ ΡΠ΅ΠΊΠΎΠΌΠ΅Π½Π΄ΠΎΠ²Π°ΡΡ Π°Π»Π³ΠΎΡΠΈΡΠΌ NLMS Π΄Π»Ρ ΡΠΈΡΡΠ΅ΠΌ ΡΠ΅Π°Π»ΡΠ½ΠΎΠ³ΠΎ Π²ΡΠ΅ΠΌΠ΅Π½ΠΈ, Π° Π°Π»Π³ΠΎΡΠΈΡΠΌ RLS β Π΄Π»Ρ ΡΠ΅Ρ
Π½ΠΈΡΠ΅ΡΠΊΠΈΡ
ΡΠΈΡΡΠ΅ΠΌ, ΡΠ°Π±ΠΎΡΠ°ΡΡΠΈΡ
Ρ Π·Π°ΠΏΠΈΡΡΠΌΠΈ ΡΠ΅ΡΠ΅Π²ΡΡ
ΡΠΈΠ³Π½Π°Π»ΠΎΠ². Π Π°ΡΡΠΌΠΎΡΡΠ΅Π½Π½ΡΠ΅ Π°Π»Π³ΠΎΡΠΈΡΠΌΡ ΠΌΠΎΠ³ΡΡ Π±ΡΡΡ ΡΡΠΏΠ΅ΡΠ½ΠΎ ΡΠ΅Π°Π»ΠΈΠ·ΠΎΠ²Π°Π½Ρ Π½Π° ΡΠΎΠ²ΡΠ΅ΠΌΠ΅Π½Π½ΡΡ
ΡΠ΅Ρ
Π½ΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΏΠ»Π°ΡΡΠΎΡΠΌΠ°Ρ
, ΡΠΎΠ΄Π΅ΡΠΆΠ°ΡΠΈΡ
Π²ΡΡΠΎΠΊΠΎΠΏΡΠΎΠΈΠ·Π²ΠΎΠ΄ΠΈΡΠ΅Π»ΡΠ½ΡΠ΅ ΡΠΈΡΡΠΎΠ²ΡΠ΅ ΡΠΈΠ³Π½Π°Π»ΡΠ½ΡΠ΅ ΠΏΡΠΎΡΠ΅ΡΡΠΎΡΡ ΠΈ ΡΠΎΠΎΡΠ²Π΅ΡΡΡΠ²ΡΡΡΡΡ ΠΏΠ΅ΡΠΈΡΠ΅ΡΠΈΡ
Technological Basis of the Formation of Micromesh Transparent Electrodes by Means of a Self-Organized Template and the Study of Their Properties
Π’Π΅ΠΊΡΡ ΡΡΠ°ΡΡΠΈ Π½Π΅ ΠΏΡΠ±Π»ΠΈΠΊΡΠ΅ΡΡΡ Π² ΠΎΡΠΊΡΡΡΠΎΠΌ Π΄ΠΎΡΡΡΠΏΠ΅ Π² ΡΠΎΠΎΡΠ²Π΅ΡΡΡΠ²ΠΈΠΈ Ρ ΠΏΠΎΠ»ΠΈΡΠΈΠΊΠΎΠΉ ΠΆΡΡΠ½Π°Π»Π°.This Letter presents the results of a study of the physical properties of micromesh transparent electrodes on a flexible substrate, obtained using a template in the form of silica layers subjected to controlled cracking. For the first time, a combined approach to the control of parameters of a micromesh structure (crack width and cell size) by varying the pH and the thickness of the sol layer is proposed. Using this approach, transparent electrodes with a surface resistance of 4.1 Ξ©/sq with a transparency of 85.7% were obtained. Micromesh electrodes are characterized by linear optical transmission in the visible and IR ranges, which opens up prospects for their use in optoelectronics
Influence of the Addition of Alumina Nanofibers on the Strength of Epoxy Resins
The paper describes the effect of the addition of alumina nanofibers on the mechanical properties of the epoxy resin. Alumina nanofibers functionalized with epoxypropyl functional groups are used in this work. The dependence of the mechanical characteristics on the amount of the additive, as well as the features of its distribution in the material, is investigated. In the work, nanocomposites were obtained, which are epoxy resin with aluminum oxide nanofibers. The mechanical properties of the samples were studied by bending tests and differential mechanical analysis (DMA). It has been shown that the addition of alumina nanofibers leads to an increase in ultimate flexural strength. The maximum of this increase is near the percolation threshold of alumina nanofibers in epoxy resin. With the addition of 0.2% alumina nanofibers, the ultimate flexural strength increases from 41 to 71 MPa. It is shown that after exceeding the percolation threshold of nanofibers, the ultimate strength decreases. In this case, the elastic modulus increases from 0.643 to 0.862 GPa. DMA is shown that the glass transition temperature decreases with increasing amount of the additive. This indicates a decrease in the molecular weight of the polymer. By implication, this suggests that the hardener connects the epoxypropyl functional groups on the nanofibers and the epoxy groups in the resin, and as a result of this process, the nanofibers become natural polymer chain length limiters. The data obtained from mechanical testing and differential mechanical analysis can be used to strengthen epoxy resins in polymer composite materials and molding compositions
Influence of the Addition of Alumina Nanofibers on the Strength of Epoxy Resins
The paper describes the effect of the addition of alumina nanofibers on the mechanical properties of the epoxy resin. Alumina nanofibers functionalized with epoxypropyl functional groups are used in this work. The dependence of the mechanical characteristics on the amount of the additive, as well as the features of its distribution in the material, is investigated. In the work, nanocomposites were obtained, which are epoxy resin with aluminum oxide nanofibers. The mechanical properties of the samples were studied by bending tests and differential mechanical analysis (DMA). It has been shown that the addition of alumina nanofibers leads to an increase in ultimate flexural strength. The maximum of this increase is near the percolation threshold of alumina nanofibers in epoxy resin. With the addition of 0.2% alumina nanofibers, the ultimate flexural strength increases from 41 to 71 MPa. It is shown that after exceeding the percolation threshold of nanofibers, the ultimate strength decreases. In this case, the elastic modulus increases from 0.643 to 0.862 GPa. DMA is shown that the glass transition temperature decreases with increasing amount of the additive. This indicates a decrease in the molecular weight of the polymer. By implication, this suggests that the hardener connects the epoxypropyl functional groups on the nanofibers and the epoxy groups in the resin, and as a result of this process, the nanofibers become natural polymer chain length limiters. The data obtained from mechanical testing and differential mechanical analysis can be used to strengthen epoxy resins in polymer composite materials and molding compositions
Features of Functionalization of the Surface of Alumina Nanofibers by Hydrolysis of Organosilanes on Surface Hydroxyl Groups
Small additions of nanofiber materials make it possible to change the properties of polymers. However, the uniformity of the additive distribution and the strength of its bond with the polymer matrix are determined by the surface of the nanofibers. Silanes, in particular, allow you to customize the surface for better interaction with the matrix. The aim of our work is to study an approach to silanization of nanofibers of aluminum oxide to obtain a perfect interface between the additive and the matrix. The presence of target silanes on the surface of nanofibers was shown by XPS methods. The presence of functional groups on the surface of nanofibers was also shown by the methods of simultaneous thermal analysis, and the stoichiometry of functional groups with respect to the initial hydroxyl groups was studied. The number of functional groups precipitated from silanes is close to the number of the initial hydroxyl groups, which indicates a high uniformity of the coating in the proposed method of silanization. The presented technology for silanizing alumina nanofibers is an important approach to the subsequent use of this additive in various polymer matrices