Teflon hydrophilic

Figure 24 shows that the values of AX derived from Figs. 14 and 15 are consistent with the values of C measured by Valette.390 On the other hand, the same values of C cannot fit Fig. 24 if the values of AX estimated by Valette389 are used. The same is the case for the values of C as reported by Popov et alm for single-crystal faces grown in a Teflon capillary. These authors observed the opposite sequence, i.e., C(111) > C(100), thus concluding that the (111) face is more hydrophilic than the (100) face. However, as pointed out earlier, they measured the same Eam0 as the other... 

The sorbents were hydrophobic Teflon, hydrophobic polystyrene (PS), and hydrophilic silica. These sorbents were negatively charged colloidal particles having smooth surfaces. In adition, PS particles at the surface of which oligomers (8-mers) of ethylene oxide ((EO)8) were grafted at a... 

The influence of adsorption on the structure of a -chymotrypsin is shown in Fig. 10, where the circular dichroism (CD) spectrum of the protein in solution is compared with that of the protein adsorbed on Teflon and silica. Because of absorbance in the far UV by the aromatic styrene, it is impossible to obtain reliable CD spectra of proteins adsorbed on PS and PS- (EO)8. The CD spectrum of a protein reflects its composition of secondary structural elements (a -helices, / -sheets). The spectrum of dissolved a-chymotrypsin is indicative of a low content of or-helices and a high content of //-sheets. After adsorption at the silica surface, the CD spectrum is shifted, but the shift is much more pronounced when the protein was adsorbed at the Teflon surface. The shifts are in opposite directions for the hydrophobic and hydrophilic surfaces, respectively. The spectrum of the protein on the hydrophilic surface of silica indicates a decrease in ordered secondary structure, i.e., the polypeptide chain in the protein has an increased random structure and, hence, a larger conformational entropy. Adsorption on the hydrophobic Teflon surface induces the formation of ordered structural elements, notably an increase in the content of O -helices (cfi, the discussion in Sect. 3.1.4). 

The enzymatic activities of O -chymotrypsin in solution and adsorbed at the different surfaces are presented in Fig. 11, where the specific enzymatic activity (defined as activity per unit mass of protein) is plotted as a function of temperature. The enzyme loses activity due to adsorption. On the hydrophobic Teflon and PS surfaces, the activity is completely gone, whereas on the hydrophilic silica surface, or-chymotrypsin has retained most of its biological function. These differences are in agreement with the adsorption isotherms and the circular dichroism spectra. The influence of the hydrophobicity of the sorbent surface on the affinity of the protein for the sorbent surface, as judged from the rising parts of the adsorption isotherms (Fig. 8), suggests that the proteins are more perturbed and, hence, less biologically active when adsorbed at hydrophobic surfaces. Also, the CD spectra indicate that adsorption-induced structural perturbations are more severe at hydrophobic surfaces. 

At the other end of the spectrum are substances that do not interact well with water oils, fats, waxes, and Teflon provide four examples. Oils are hquids that create films on the surface of water many are hydrocarbons. Fats, waxes, and Teflon, a fluorocarbon polymer, are solids upon which water beads. Think about what the waxed hood of your car looks like after rain. Substances in this class are hydrophobic. We have a spectrum extending from very hydrophilic substances, on the one hand, to very hydrophobic ones, on the other hand. There is a comfortable middle ground and many substances are balanced in their hydrophobic/hydrophilic character. 

PFCs comprise a large group of compounds characterized by a fully fluorinated hydrophobic linear carbon chain attached to one or more hydrophilic head. PFCs repel both water and oil, and are therefore ideal chemicals for surface treatments. These compounds have been used for many industrial applications including stain repellents (such as Teflon), textile, paints, waxes, polishes, electronics, adhesives, and food packaging [1]. 

Naneva and Popov et al. [4, 5] have studied Cd(OOOl) grown electrolytically in a Teflon capillary in NaF aqueous solution. A value of fpzc equal to —0.99 V (versus saturated calomel electrode (SCE)) was evaluated from minimum potential (Amin) on the differential capacity C-E curves obtained in dilute electrolyte. The zero charge potential was found to be practically independent of the crystallographic orientation. The Apzc and the irmer layer capacity of Cd(OOOl) single crystals were determined in KF solution as a function of temperature [5]. The positive values of AApzc/AT indicated that the water dipoles in the inner part of the double layer were orientated with their negative part to the electrode surface. It was found that the hydrophilicity of the electrodes was increasing in the order Cd(OOOl) < Ag(100)[Pg.768]

Membrane materials often employed are hydrophobic polysulfone or hydrophilic regenerated cellulose or cellulose acetate other materials are nylon, polytetrafluoro-ethylene (PTFE, Teflon), polyether ether ketone (PEEK) or poly(divinyl fluoride) (PDVF). 

Examination of the relevant theory indicates that the adjuvant effect of surface-active agents on herbicide action is maximized when the quantity FI = yL cos 0, or the film pressure at the liquid/solid interface, has a maximum value. Measurement of surface tension of 1.0% aqueous solutions and of contact angle on a number of substrates (Teflon, paraffin) and plant-leaf surfaces (soybean, com) as a function of hydrophile-lipophile balance show at least one maximum, and these values are in good agreement with earlier experimental data on herbicidal activity. 

For PEMFCs, the solid electrolytes are polymer membranes polymers modified to include ions, usually sulfonic groups. One of the most widely used membranes today is the polymer Nafion , created by the DuPont company. These membranes have aliphatic perfluorinated backbones with ether-linked side chains ending in sulfonate cation exchange groups [6, 7], Nafion is a copolymer of tetrafluoroethylene and sulfonyl fluoride vinyl ether [8] and has a semi-crystalline structure [9], This structure (which resembles Teflon ) gives Nafion long-term stability in oxidative or reductive conditions. The sulfonic groups of the polymers facilitate the transport of protons. The polymers consist of hydrophilic and hydrophobic domains that allow the transport of protons from the anode to the cathode [10, 11],... 

On evaporation the solvent often creeps up the walls of a glass vessel, because the silicate OH-groups make glass hydrophilic. Therefore nucleation occurs outside the solution this never gives good crystals and can be avoided by using polypropylene or Teflon vessels. 

A highly hydrophobic polymer such as Teflon PFA has weak x interaction with water. The y interaction is strong in liquid water but very weak in contact with water vapor. When the hydrophilicity of polymer increases the contribution of the x interaction increases, and the relative contribution of the y interaction changes according to the value of A(yg). 

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