Carbonization technique, modification

For all of the causes described above, in addition to traditional and relatively simple methods of carbon surface modifications (e.g., oxidation in liquid or gaseous phases), more sophisticated approaches are proposed which employ newly developed techniques such as intercalation [46,47], chemical vapor deposition (CVD) [48,49], and self-assembly of molecules [50]. 

Cross-sectional modifications of a more extreme nature than skin-bursting, which nevertheless do not form crimp, have grown in importance since the early 1980s. These yield a permanent bulk increase which can be translated into bulky fabrics without the need for special care. The first commercial staple fiber of this type was Courtaulds hoUow Viloft, developed in the 1970s using a carbonate inflation technique (37). 

Manufacture. Several methods have been described for the preparation of -hydroxyben2oic acid. The commercial technique is similar to that of salicylic acid, ie, Kolbe-Schmitt carboxylation of phenol. The modification includes the use of potassium hydroxide in place of caustic (51). The dried potassium phenate is heated under pressure, 270 kPa (2.7 atm) or more, with dry carbon dioxide at 180—250°C. The potassium salt [16782-08-4] of Nhydroxyben2oic acid forms almost quantitatively and can be converted to free acid by using a mineral acid. 

Two-dimensional C//correlations such as C//COSY or HC HMQC and HSQC provide the Jqh connectivities, and thereby apply only to those C atoms which are linked to H and not to non-protonated C atoms. Modifications of these techniques, also applicable to quaternary C atoms, are those which are adjusted to the smaller Jqh and Jqh couplings (2-25 Hz, Tables 2.8 and 2.9) Experiments that probe these couplings include the CH COLOC (correlation via long range couplings) with carbon-13 detection (Fig. 2.16) and HC HMBC (heteronuclear multiple bond coherence) with the much more sensitive proton detection (Fig. 2.17)... 

Sol-gel technique has also been applied to modify the anode/electrolyte interface for SOFC running on hydrocarbon fuel [16]. ANiA SZ cermet anode was modified by coating with SDC sol within the pores of the anode. The surface modification of Ni/YSZ anode resulted in an increase of structural stability and enlargement of the TPB area, which can serve as a catalytic reaction site for oxidation of carbon or carbon monoxide. Consequently, the SDC coating on the pores of anode leads to higher stability of the cell in long-term operation due to the reduction of carbon deposition and nickel sintering. 

Modification techniques for activated carhon were used to increase the removal capacity by surface adsorption and to improve the selectivity to volatile organic compounds (VOCs). Modified activated carbons (MACs) were prepared by modifying the purified activated carbon with various acids or bases. The effects of adsorption capacity and modified contents on the textural properties of the MACs were investigated. Furthermore, VOC adsorption and desorption experiments were carried out to determine the relationship between the adsorption capacity and the chemical properties of the adsorbents. High adsorption capacity for the selected VOCs was obtained over lwt%-H3P04/AC (lwt%-PA/AC). As a result, MAC was found to be very effective for VOC removal by adsorption with the potential for repeated use through desorption by simple heat treatment. 

Several techniques for VOC removal have been investigated such as thermal incineration, catalytic oxidation, condensation, absorption, bio-filtration, adsorption, and membrane separation. VOCs are present in many types of waste gases and are often removed by adsorption [1]. Activated carbon (AC) is commonly used as an adsorbent of gases and vapors because of its developed surface area and large pore volumes [2]. Modification techniques for AC have been used to increase surface adsorption and hence removal capacity, as well as to improve selectivity to organic compounds [3]. 

It must be acknowledged, however, that the determination of the number of the different surface species which are formed during an adsorption process is often more difficult by means of calorimetry than by spectroscopic techniques. This may be phrased differently by saying that the resolution of spectra is usually better than the resolution of thermograms. Progress in data correction and analysis should probably improve the calorimetric results in that respect. The complex interactions with surface cations, anions, and defects which occur when carbon monoxide contacts nickel oxide at room temperature are thus revealed by the modifications of the infrared spectrum of the sample (75) but not by the differential heats of the CO-adsorption (76). Any modification of the nickel-oxide surface which alters its defect structure produces, however, a change of its energy spectrum with respect to carbon monoxide that is more clearly shown by heat-flow calorimetry (77) than by IR spectroscopy. 

The dispersion and solid-state ion exchange of ZnCl2 on to the surface of NaY zeolite by use of microwave irradiation [17] and modification of the surface of active carbon as catalyst support by means of microwave induced treatment have also been reported [18]. The ion-exchange reactions of both cationic (montmorillonites) and anionic clays (layered double hydroxides) were greatly accelerated under conditions of microwave heating compared with other techniques currently available [19.]... 

The physicochemical basis behind the technique of radiocarbon dating is the isotopic abundances of carbon s three isotopes 12C is the normal form and constitutes 98.9 per cent of all naturally occurring carbon. 13 C is the other naturally occurring isotope, with an abundance of about 1 per cent. 14C does not occur naturally, but tiny amounts of it are formed when high-energy particles from space collide with gases in the upper atmosphere, thus causing radiochemical modification. 

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