A Comprehensive Analysis of Inorganic Ions and Their Selective Removal from the Reconstituted Tobacco Extract Using Electrodialysis.

Many tobacco stalks, dust, and fines are discharged in the tobacco industry, rich in inorganic minerals ions and nicotine salts. The high salinity and nicotine salts are challenging to be addressed by traditional treatment and are a severe threat that ought to be overcome. Thus, proper techniques can regenerate the tobacco stalks into reconstituted tobacco flakes used as cigarette filler.

[Study on the inclusion behavior of p-sulphonatocalix[4]arene with acridine by spectrofluorometric titrations].

p-sulphonatocalix[4] arene (1) was prepared according to the literature, and spectrofluorometric titrations were performed to investigate the inclusion behavior of (1) and acridine in citrate buffer solution (pH 5.92, 0.1 mol x L(-1)) at different temperatures.

Study on the inclusion behavior of p-sulphonatocalix[4]arene with 9-amino-acridine by spectrofluorometric titrations.

Spectrofluorometric titrations have been performed to investigate the inclusion behavior of p-sulphonatocalix[4]arene (SC4A) and 9-amino-acridine (AA) in citrate buffer solution (pH 5.92). It was found that the fluorescence intensity of AA quenched regularly upon the addition of SC4A.

[Spectrum studies and application of the reaction system phenanthroline-EBT-H2O2].

A kinetic spectrophotometric method for the determination of trace phenanthroline was proposed. The method is based on the inhibition of phenanthroline to the discoloring reaction of EBT oxidized by hydrogen peroxide in the dilute acetic acid solution. At the same time, the kinetic parameters were studied in detail.

Spectrofluorimetric study on the inclusion interaction between lomefloxacin and p-sulfonated calix[4]arene and its analytical application.

The characteristics of host-guest complexation between p-sulfonated calix[4]arene (SC4A) and lomefloxacin (LMFX) were investigated by fluorescence spectrometry. A 1:1 stoichiometry for the complexation was established and an association constant of 6.48x10(4) l mol-1 at 25 degrees C was calculated by applying a deduced equation.

[Highly sensitive spectrofluorimetric determination of trace amounts of nitrite with N-(1-naphthyl) ethylenediamine].

A simple and sensitive fluorescence quenching method for the determination of trace nitrite was developed. The method is based on the reaction of NED with nitrite in acidic medium to form a new compound, which has weak fluorescence. The linear range was 1.

Preparation of fluorescent polyvinyl alcohol keto-derivatives nanoparticles and selective determination of chromium(VI).

A novel fluorescent polyvinyl alcohol keto-derivatives nanoparticle (PVAK) has been prepared in one-step method. The nanoparticles has excitation and emission maxima at 349 and 462 nm, respectively. Based on the fluorescence quenching of PVAK by Cr(VI), we established a simple and selective fluorimetric method for the determination of Cr(VI) without separation of Cr(III) in water.

[Highly sensitive spectrofluorimetric determination of trace amounts of chromium (VI) with mono[6-o-(4-aminobenzoic acid)]-beta-cyclodextrin].

A novel fluorescence probe, mono[6-o-(4-aminobenzoic acid)]-beta-cyclodextrin(ACD), was synthesized, and a new sensitive fluorescence identification reaction was studied based on the reaction of Cr2O7(2-) with compound ACD in NaAc-HAc buffer medium at pH 4.90. Under optimal conditions the determination limit was 1.

Direct fluorimetric determination of ascorbic acid by the supramolecular system of AA with beta-cyclodextrin derivative.

We established a simple and selective fluorimetric method for the determination of ascorbic acid (AA) with the novel mono-[6-N(4-carboxy-phenyl)]-beta-cyclodextrin (ACD). The method is based on the fluorescence intensity of ACD decreases as the ACD-AA supramolecular complexes form. The fluorescence intensity is measured at excitation and emission wavelengths of 270 and 352 nm, respectively.