11 research outputs found
ΠΠΊΡΠΏΠ΅ΡΠΈΠΌΠ΅Π½ΡΠ°Π»ΡΠ½ΠΎΠ΅ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΠ΅ ΠΏΡΠΎΡΠ΅ΡΡΠΎΠ² ΠΊΠΈΠΏΠ΅Π½ΠΈΡ ΠΈ ΠΈΡΠΏΠ°ΡΠ΅Π½ΠΈΡ ΡΠΎΠ½ΠΊΠΈΡ ΡΠ»ΠΎΠ΅Π² ΠΆΠΈΠ΄ΠΊΠΎΡΡΠΈ
ΠΠ±ΡΠ΅ΠΊΡΠΎΠΌ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ ΡΠ²Π»ΡΠ΅ΡΡΡ ΠΏΡΠΎΡΠ΅ΡΡ ΠΈΡΠΏΠ°ΡΠ΅Π½ΠΈΡ ΡΠΎΠ½ΠΊΠΎΠ³ΠΎ ΡΠ»ΠΎΡ ΠΆΠΈΠ΄ΠΊΠΎΡΡΠΈ Ρ ΡΠ²Π΅ΡΠ΄ΠΎΠΉ ΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΠΈ.
Π¦Π΅Π»Ρ ΡΠ°Π±ΠΎΡΡ β ΡΠΊΡΠΏΠ΅ΡΠΈΠΌΠ΅Π½ΡΠ°Π»ΡΠ½ΠΎΠ΅ ΠΎΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΈΠ΅ Π·Π°Π²ΠΈΡΠΈΠΌΠΎΡΡΠ΅ΠΉ ΡΠΊΠΎΡΠΎΡΡΠΈ ΠΈΡΠΏΠ°ΡΠ΅Π½ΠΈΡ ΡΠ»ΠΎΡ ΠΆΠΈΠ΄ΠΊΠΎΡΡΠΈ ΠΈ ΠΊΠΎΡΡΡΠΈΡΠΈΠ΅Π½ΡΠ° ΡΠ΅ΠΏΠ»ΠΎΠΎΡΠ΄Π°ΡΠΈ ΠΎΡ ΡΠ΅ΠΌΠΏΠ΅ΡΠ°ΡΡΡΡ ΠΏΠΎΠ΄Π»ΠΎΠΆΠΊΠΈ ΠΈ ΡΠΎΡΡΠ°Π²Π° ΠΆΠΈΠ΄ΠΊΠΎΡΡΠΈ.
Π ΠΏΡΠΎΡΠ΅ΡΡΠ΅ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ ΠΏΡΠΎΠ²ΠΎΠ΄ΠΈΠ»ΠΈΡΡ ΡΠΊΡΠΏΠ΅ΡΠΈΠΌΠ΅Π½ΡΠ°Π»ΡΠ½ΡΠ΅ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ ΠΏΠΎ ΠΎΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΈΡ Π·Π°Π²ΠΈΡΠΈΠΌΠΎΡΡΠ΅ΠΉ ΡΠΎΠ»ΡΠΈΠ½Ρ ΡΠ»ΠΎΡ ΠΆΠΈΠ΄ΠΊΠΎΡΡΠΈ ΠΎΡ Π²ΡΠ΅ΠΌΠ΅Π½ΠΈ, ΠΌΠ°ΡΡΠΎΠ²ΠΎΠΉ ΡΠΊΠΎΡΠΎΡΡΠΈ ΠΈΡΠΏΠ°ΡΠ΅Π½ΠΈΡ ΠΎΡ ΡΠΎΠ»ΡΠΈΠ½Ρ ΡΠ»ΠΎΡ ΠΆΠΈΠ΄ΠΊΠΎΡΡΠΈ, ΠΊΠΎΡΡΡΠΈΡΠΈΠ΅Π½ΡΠ° ΡΠ΅ΠΏΠ»ΠΎΠΎΡΠ΄Π°ΡΠΈ ΠΎΡ Π²ΡΠ΅ΠΌΠ΅Π½ΠΈ, Π½Π°Π»ΠΈΡΠΈΡ ΠΈ Π²Π΅Π»ΠΈΡΠΈΠ½Π΅ ΡΠ΅ΠΌΠΏΠ΅ΡΠ°ΡΡΡΠ½ΠΎΠ³ΠΎ ΠΏΠ΅ΡΠ΅ΠΏΠ°Π΄Π° Π½Π° ΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΠΈ ΡΠ°Π·Π΄Π΅Π»Π° ΡΠ°Π·.
ΠΠΎΠ»ΡΡΠ΅Π½Π½ΡΠ΅ ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΡ ΠΌΠΎΠ³ΡΡ Π±ΡΡΡ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½Ρ ΠΏΡΠΈ ΡΠ°Π·ΡΠ°Π±ΠΎΡΠΊΠ΅ Π½Π°ΡΡΠ½ΡΡ
ΠΎΡΠ½ΠΎΠ² ΠΏΡΠΎΠ΅ΠΊΡΠΈΡΠΎΠ²Π°Π½ΠΈΡ ΠΏΠ»Π΅Π½ΠΎΡΠ½ΡΡ
ΡΠ΅Π³Π°Π·ΠΈΡΠΈΠΊΠ°ΡΠΎΡΠΎΠ², Π° ΡΠ°ΠΊΠΆΠ΅ ΡΠΈΡΡΠ΅ΠΌ ΠΎΠ±Π΅ΡΠΏΠ΅ΡΠ΅Π½ΠΈΡ ΡΠ΅ΠΏΠ»ΠΎΠ²ΠΎΠ³ΠΎ ΡΠ΅ΠΆΠΈΠΌΠ° ΡΠ»Π΅ΠΊΡΡΠΎΠ½Π½ΠΎΠ³ΠΎ ΠΈ Π°Π²ΠΈΠ°ΠΊΠΎΡΠΌΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΠΎΠ±ΠΎΡΡΠ΄ΠΎΠ²Π°Π½ΠΈΡ.The object of research is the process of evaporation of a thin layer of a liquid on a solid surface.
The aim of this work - experimental determination of the dependency rate of evaporation of the liquid layer and the heat transfer coefficient on the substrate temperature and fluid composition.
During the experimental studies studies were carried out to determine the liquid layer thickness dependency of the time, the mass evaporation rate of the liquid layer thickness, the heat transfer coefficient to time, the presence and magnitude of the temperature drop at the interface.
The results can be used in the development of scientific bases of designing film regasificators, and thermal control systems of electronic and aerospace equipment
The interrelation between the electronic parameters of nitrogen atom and intramolecular interactions in ammonia derivatives
The electronic parameters and intramolecular interactions in the ground and transition states of inversion of the amines HβNXHn (XHn=CHβ, NHβ, OH, F, SiHβ, PHβ, SH, Cl) were calculated using DFT (PBE96/def2-tzvpp) method. It was established that the electronacceptor properties of the XHn substituents has a prevailing influence on the change of the electronic parameters of nitrogen atom. Its increase leads to both a decrease of the charge on the nitrogen atom and an increase of the s-character and population of nitrogen lone pair (LP). All parameters under consideration correlate with the Ο- and Οα΅’-constants of the XHn substituents. The correlation coefficients increase when amines that contain X atoms only from one period are considered separately. It was found that the Ο values for amines containing X atoms from the second or third period are substantially different. The changes of the donor-acceptor interaction energies, s-character and LP population cannot be probable causes for different sensitivity of the electronic parameters of amines containing X atoms from different periods to the change of electron-acceptor properties of the XHn substituents. It was established that the mentioned parameters has only a subordinated influence in comparison with the influence of electron-acceptor ability of the XHn substituents. The negative charge on the nitrogen atom decreases with the increase of s-character and LP population and also with the decrease of energies of donor-acceptor interactions which lead to the withdrawal of electron density from the nitrogen atom. The s-character and LP population increase with the decrease of energies of donor-acceptor interactions which result in the reduction of electron density on the nitrogen atom. The total positive charges of the XHn groups and hydrogen atoms at the nitrogen atom decrease with increasing the electron-acceptor ability of the XHn substituents. The representation of the electron-acceptor properties of the substituents was shown to be more valid by using the Ο-constants than by using the Οα΅’-constants. The chlorine atom is a weak electron acceptor in comparison with an amino group