div class="wrap-content-read table-responsive">able-responsive">le-responsive">-responsive">esponsive">ponsive">nsive">">01lassSurface chemistry studies such phenomena as damping, adhesion, sorption and surface tension.rface chemistry studies such phenomena as damping, adhesion, sorption and surface tension.ace chemistry studies such phenomena as damping, adhesion, sorption and surface tension.ng, adhesion, sorption and surface tension., adhesion, sorption and surface tension.adhesion, sorption and surface tension.hesion, sorption and surface tension.sion, sorption and surface tension.on, sorption and surface tension., sorption and surface tension.rption and surface tension.tion and surface tension.on and surface tension.nd surface tension. surface tension.ce tension. tension.ension.classasss(σ) is defined as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.sigma;) is defined as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.gma;) is defined as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.a;) is defined as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.) is defined as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.is defined as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.fined as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.ned as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.d as energy per unit area, [J/m²], or the force that causes the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.ses the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.s the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.the surface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.rface of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.ace of a liquid to contract [N/m]. Among the pure liquids, Hg has a maximum value of σ. 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Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.ids, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.s, Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system. Hg has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.g has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.has a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.s a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.a maximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.ximum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.mum value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.m value of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.lue of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.e of σ. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.sigma;. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.gma;. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.a;. Among the biological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.iological fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.logical fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.gical fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.al fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system. fluids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.luids, H₂O has a maximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.ximum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.mum value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.m value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.value of σ, and dissolved substances may either increase or decrease this constant, forming a new system.lue of σ, and dissolved substances may either increase or decrease this constant, forming a new system.e of σ, and dissolved substances may either increase or decrease this constant, forming a new system.σ, and dissolved substances may either increase or decrease this constant, forming a new system.igma;, and dissolved substances may either increase or decrease this constant, forming a new system.ma;, and dissolved substances may either increase or decrease this constant, forming a new system.constant, forming a new system.nstant, forming a new system.tant, forming a new system.forming a new system.rming a new system.ing a new system.bs’ energy (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.’ energy (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.squo; energy (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.uo; energy (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.; energy (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.energy (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ergy (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. (G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.G) tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. tends to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ds to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. to the minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.e minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.minimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.nimum (ΔG <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. <0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.lt;0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.;0 for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.for the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.r the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.the spontaneous process), the surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.surface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.rface Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ace Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.e Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.Gibbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.bbs’ energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.squo; energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.uo; energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.; energy G_S = σ ∙ S → min, and for pure liquids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.uids S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ds S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. S → min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.rr; min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.; min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.min is the only way to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ay to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. to decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.o decrease free surface energy, that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. that is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.hat is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.t is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.is why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. why liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.hy liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. liquids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.uids form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ds form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. form drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.m drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.drops. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. The greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.he greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. greater σ — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.; — the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.— the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.dash; the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.h; the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. the bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.he bigger drop may be formed, thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.thus the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.us the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. the number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.he number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. number of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.umber of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. of drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.f drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.drops in the certain volume is less. This method is often used to find the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ind the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.d the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.the value of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.lue of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.e of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.of σ in either pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.her pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.r pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.pure solvents or solutions including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ons including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.s including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.including biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.cluding biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.uding biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ing biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.g biological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ological fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ogical fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface.ical fluids and drugs. Surface tension (σ) depends on t°, pressure, the polarity of phases, concentration and nature of solutes (or admixtures). Here is another way to decrease free surface energy (G_S): the component with a lesser value of σ is pushed out, onto the surface. fluids and drugs. 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ГЛАВА 15. РАК СЛИЗИСТОЙ ОБОЛОЧКИ ПОЛОСТИ РТА И ЯЗЫКА

ГЛАВА 16. РАК СЛИЗИСТОЙ ОБОЛОЧКИ КЛЕТОК РЕШЕТЧАТОГО ЛАБИРИНТА, ПОЛОСТИ НОСА И ПРИДАТОЧНЫХ ПАЗУХ

ГЛАВА 17. РАК МОЛОЧНОЙ ЖЕЛЕЗЫ

ГЛАВА 18. РАК ЛЕГКОГО

ГЛАВА 19. РАК ПИЩЕВОДА

ГЛАВА 20. РАК ЖЕЛУДКА

ГЛАВА 21. КОЛОРЕКТАЛЬНЫЙ РАК

ГЛАВА 22. РАК ПОДЖЕЛУДОЧНОЙ ЖЕЛЕЗЫ

ГЛАВА 23. РАК ПЕЧЕНИ

ГЛАВА 24. ОНКОГИНЕКОЛОГИЯ

ГЛАВА 25. ОНКОУРОЛОГИЯ

ГЛАВА 26. ОПУХОЛИ КРОВЕТВОРНОЙ СИСТЕМЫ

ЛИТЕРАТУРА

ДОПОЛНИТЕЛЬНЫЕ ИЛЛЮСТРАЦИИ

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1. Пигментные невусы: а - внутридермальный; б - врожденный клеточный; в - врожденный «кофе с молоком»; г - приобретенный

Рис. 2. Дерматофиброма

Рис. 3. Меланома

• Каталог
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Онкология

Оглавление

АВТОРСКИЙ КОЛЛЕКТИВ

ПРЕДИСЛОВИЕ

ГЛАВА 1. ЭПИДЕМИОЛОГИЯ. ОРГАНИЗАЦИЯ ОНКОЛОГИЧЕСКОЙ СЛУЖБЫ

ГЛАВА 2. КЛАССИФИКАЦИЯ И ОБЩАЯ ХАРАКТЕРИСТИКА ОПУХОЛЕЙ. КАНЦЕРОГЕНЕЗ

ГЛАВА 3. ФАКТОРЫ РИСКА ВОЗНИКНОВЕНИЯ ЗЛОКАЧЕСТВЕННЫХ ОПУХОЛЕЙ

ГЛАВА 4. ПРОФИЛАКТИЧЕСКИЕ МЕРОПРИЯТИЯ В ОНКОЛОГИИ

ГЛАВА 5. ОБЩИЕ ПРИНЦИПЫ РАННЕЙ И СВОЕВРЕМЕННОЙ ДИАГНОСТИКИ ЗЛОКАЧЕСТВЕННЫХ ОПУХОЛЕЙ

ГЛАВА 6. МЕТОДЫ ЛЕЧЕНИЯ В ОНКОЛОГИИ

ГЛАВА 7. ПАЛЛИАТИВНАЯ ПОМОЩЬ В ОНКОЛОГИИ

ГЛАВА 8. НЕОТЛОЖНЫЕ СОСТОЯНИЯ В ОНКОЛОГИИ

ГЛАВА 9. ОПУХОЛИ КОЖИ

ГЛАВА 10. ОПУХОЛИ МЯГКИХ ТКАНЕЙ И КОСТЕЙ

ГЛАВА 11. РАК ГОРТАНИ И ГОРТАНОГЛОТКИ

ГЛАВА 12. РАК ЩИТОВИДНОЙ ЖЕЛЕЗЫ

ГЛАВА 13. ОПУХОЛИ СЛЮННЫХ ЖЕЛЕЗ

ГЛАВА 14. РАК ГУБЫ

ГЛАВА 15. РАК СЛИЗИСТОЙ ОБОЛОЧКИ ПОЛОСТИ РТА И ЯЗЫКА

ГЛАВА 16. РАК СЛИЗИСТОЙ ОБОЛОЧКИ КЛЕТОК РЕШЕТЧАТОГО ЛАБИРИНТА, ПОЛОСТИ НОСА И ПРИДАТОЧНЫХ ПАЗУХ

ГЛАВА 17. РАК МОЛОЧНОЙ ЖЕЛЕЗЫ

ГЛАВА 18. РАК ЛЕГКОГО

ГЛАВА 19. РАК ПИЩЕВОДА

ГЛАВА 20. РАК ЖЕЛУДКА

ГЛАВА 21. КОЛОРЕКТАЛЬНЫЙ РАК

ГЛАВА 22. РАК ПОДЖЕЛУДОЧНОЙ ЖЕЛЕЗЫ

ГЛАВА 23. РАК ПЕЧЕНИ

ГЛАВА 24. ОНКОГИНЕКОЛОГИЯ

ГЛАВА 25. ОНКОУРОЛОГИЯ

ГЛАВА 26. ОПУХОЛИ КРОВЕТВОРНОЙ СИСТЕМЫ

ЛИТЕРАТУРА

ДОПОЛНИТЕЛЬНЫЕ ИЛЛЮСТРАЦИИ

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