bond strength - definition. What is bond strength
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STRENGTH OF A CHEMICAL BOND
Bond strength; Bond Energy; Bond Strengths; Bond strengths; Bonding energy; Bonding strength; Bond energy (chemistry); Bond strength (chemistry); Bond energies

Bond energy         
In chemistry, bond energy (BE), also called the mean bond enthalpyClark, J (2013), BOND ENTHALPY (BOND ENERGY), Chemguide,
Physical strength         
  • A common method of physical strength training
MEASURE OF A HUMAN'S EXERTION OF FORCE ON PHYSICAL OBJECTS
Muscular strength; Arm strength; Muscular Strength
Physical strength is the measure of a human's exertion of force on physical objects. Increasing physical strength is the goal of strength training.
compressive strength         
  • Barrelling
  • Compressive strength test of concrete in UTM
  • Figure 1: microcrack nucleation and propagation
  • shear band formation
  • A cylinder being crushed under a UTM
  • 183x183px
CAPACITY OF A MATERIAL OR STRUCTURE TO WITHSTAND LOADS TENDING TO REDUCE SIZE, WHICH WITHSTANDS LOADS TENDING TO ELONGATE
Compression strength; Compressional strength; Compressive strength test; Crushing strength; Compressive strengths; Compressive Strength Test; Ultimate compressive strength
¦ noun the resistance of a material to breaking under compression. Compare with tensile strength.

ويكيبيديا

Bond energy

In chemistry, bond energy (BE), also called the mean bond enthalpy or average bond enthalpy is a measure of bond strength in a chemical bond. IUPAC defines bond energy as the average value of the gas-phase bond-dissociation energy (usually at a temperature of 298.15 K) for all bonds of the same type within the same chemical species.

The bond dissociation energy (enthalpy) is also referred to as bond disruption energy, bond energy, bond strength, or binding energy (abbreviation: BDE, BE, or D). It is defined as the standard enthalpy change of the following fission: R - X → R + X. The BDE, denoted by Dº(R - X), is usually derived by the thermochemical equation,

D ( R X )   = Δ H f ( R ) + Δ H f ( X ) Δ H f ( R X ) {\displaystyle {\begin{array}{lcl}\mathrm {D^{\circ }(R-} X)\ =\Delta H_{f}^{\circ }\mathrm {(R)} +\Delta H_{f}^{\circ }(X)-\Delta H_{f}^{\circ }(\mathrm {R} X)\end{array}}}

The enthalpy of formation ΔHfº of a large number of atoms, free radicals, ions, clusters and compounds is available from the websites of NIST, NASA, CODATA, and IUPAC. Most authors prefer to use the BDE values at 298.15 K.

For example, the carbon–hydrogen bond energy in methane BE(C–H) is the enthalpy change (∆H) of breaking one molecule of methane into a carbon atom and four hydrogen radicals, divided by four. The exact value for a certain pair of bonded elements varies somewhat depending on the specific molecule, so tabulated bond energies are generally averages from a number of selected typical chemical species containing that type of bond.

Bond energy (BE) is the average of all bond-dissociation energies of a single type of bond in a given molecule. The bond-dissociation energies of several different bonds of the same type can vary even within a single molecule. For example, a water molecule is composed of two O–H bonds bonded as H–O–H. The bond energy for H2O is the average of energy required to break each of the two O–H bonds in sequence:

H O H H + O H , D 1 O H O + H , D 2 H O H H + O + H , D = ( D 1 + D 2 ) / 2 {\displaystyle {\begin{array}{lcl}\mathrm {H-O-H} &\rightarrow &\mathrm {H\cdot +\cdot O-H} &,D_{1}\\\mathrm {\cdot O-H} &\rightarrow &\mathrm {\cdot O\cdot +\cdot H} &,D_{2}\\\mathrm {H-O-H} &\rightarrow &\mathrm {H\cdot +\cdot O\cdot +\cdot H} &,D=(D_{1}+D_{2})/2\\\end{array}}}

Although the two bonds are the equivalent in the original symmetric molecule, the bond-dissociation energy of an oxygen–hydrogen bond varies slightly depending on whether or not there is another hydrogen atom bonded to the oxygen atom.

When the bond is broken, the bonding electron pair will split equally to the products. This process is called homolytic bond cleavage (homolytic cleavage; homolysis) and results in the formation of radicals.