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The efficiency of reactive dyes adsorption onto chitin under dynamic conditions was determined. The research was carried out in an air-lift reactor. A reactive dye with chlorotriazine moiety - Black DN was reactor. A reactive dye with chlorotriazine moiety - Black DN was used. The effect of inlet Black DN concentration, chitin concentration in the reactor and flow rate on the maximum adsorption capacity of chitin under dynamic conditions, on the utilisation of the adsorption capacity of chitin and on the real working time of the reactor were investigated. The results showed that the maximum adsorption capacity of chitin was affected most by inlet dye concentration. The utilisation of the adsorption capacity of chitin, at the assumed effectiveness of dye removal, depended on inlet dye concentration and chitin concentration in the reactor. The highest efficiency was obtained at the chitin concentration in the reactor of 5 g/dm3, inlet dye concentration of 100 mg/dm3 and flow rate of 0.1 V/h.
Adsorption of reactive dyes and surfactants onto chitin from mixtures containing surfactants at constant concentration and dyes at variable concentration was investigated in the present study. Two vinylsulfonate dyes (Scarlet R, Brillantorange 3R); chlorotriazine dye (Black DN); anionic (Borutosol KRN, Siarczanol N-2) and non-ionic (Rokafenol N-8) surfactants were tested. The experiments were carried out without and with pH adjustment. The research have proved that at pH 6.2 and in surfactants presence the adsorption of vinyl-sulfonate dyes onto chitin was lower than without surfactants (control sample). It was observed that the maximum adsorption capacity of chitin in mixtures of Scarlet R and surfactants was about 3-fold lower than without surfactants and in mixtures of Brillantorange 3R and surfactants was from 2.5 to 4.1-fold lower than in control sample. At pH 3.0 the differences between maximum adsorption capacity of chitin for dyes from aqueous solutions and containing surfactants ranged from 2% (in mixture of Brillantorange 3R and Borutosol KRN) to 23% (in mixture of Scarlet R and Siarczanol N-2). The maximum adsorption capacity of chitin for Black DN (chlorotriazyne dye) in surfactants presence (from 140 to 290 mg/dm3 ) was higher at pH 6.2 as well as at pH 3.0 in comparison to control sample. Rokafenol N-8 was adsorbed the weakest onto chitin from among tested surfactants. At pH 3.0 for vinyl-sulfonate dyes the relationships between mass proportion of dye and surfactant adsorbed onto chitin (Qdye/QSAA* ) and initial concentration proportion of dye and surfactant in solution (Cdye/CSAA) was nearly linear. This indicates that dyes competed with surfactants of active sites of chitin. SAA* – Surface Active Agent (s)
The adsorption of reactive dye mixtures onto chitin modified with 5N KOH was investigated. Three binary mixtures were tested. Each mixture contained Blue D-5RN and either Yellow D-5GN, or Red D-8B or Black DN as the second dye. The tests were conducted without pH adjustment and after pH adjustment to 3.0. The results were based on the constants determined from double Langmuir isotherm. The maximum adsorption capacity of Blue D-5RN (control sample) in the samples without pH adjustment accounted for 97 mg/g d.w., and in the sample with pH adjustment (pH=3) – for 205 mg/g d.w. The adsorption capacity of a mixture of Red D-8B and Blue D-5RN reached 93 and 196 mg/g d.w., respectively, and in a mixture containing Yellow D-5GN – 103 and 214 mg/g d.w., respectively. The dye competition in a mixture was evaluated comparing 7 constants in Langmuir equation for mixtures and Blue D-5RN in a mixture. The adsorption capacity of Blue D-5RN in a mixture was found to be by ca. 8.8 % lower than the adsorption capacity of a dye mixture in the samples without pH adjustment and by ca. 9.4 % lower compared to the samples with adjusted pH. An explicit decline in K1 value was also observed, depending on the type of the second dye and pH. Blue D-5RN and Red D-8B characterized by a high similarity of chemical structure competed for active sites more strongly. It was confirmed by a higher (ca. 9-fold and 2.1-fold -pH=3) decrease in constants K determined for Blue D-5RN in a mixture. The experimental data showed that in the samples with pH=3, the competition for active sites between dyes was weaker.
The effect of chitin preparation with HCl (chitin A) and with HCl and KOH (chitin B) and pH on the adsorption of reactive dyes (helactine, polactine and remazol) on chitin was investigated. The double Lang- muir equation was appropriate to analyze the dependence between amount of the adsorbed dye on chitin (Q) and its equilibrium concentration (C). It indicated the presence of two types of active sites which differed in both the maximum adsorption capacity (b) and adsorption affinity (K). Based on the dimensionless separa­tion factor R it was found that the dye adsorption mechanism in type I sites was an ion exchange, whereas in the case of type II sites it was a physical adsorption. The adsorption capacity of the chitin A (deacetylation degree of 3%) for samples without pH adjustment ranged from 29 (Red D-8B) to 67 mg/g dry weight of chitin (Gelb GR). At pH 3.0 the adsorption capacity was higher from 1.9 to 2.3-fold. The most favourable effect of pH change was found for helactine dyes. The adsorption capacity of the chitin B (deacetylation degree of 5%) was from 66 (Brillantorange 3R) to 101 mg/g dry weight of chitin (Gelb GR). After pH adjustment to pH 3.0 the adsorption capacity ranged from 160 (Ruby F-2B) to 294 mg/g dry weight of chitin (Blau 3R). The most favourable effect of deacety- lation degree increase was found in the case of helactine dyes in the samples without pH adjustment, and polactine and remazol dyes at pH 3.0.
The adsorption of reactive dyes onto chitin (deacetylation degree = 5%) was investigated from aqueous solutions at pH 3. Ten reactive dyes were examined, including 5 dyes from the helactine group, 3 dyes from the polactine group and 2 dyes from the remazol group. The K and b constants were calculated from the Langmuir equation that assumes the presence of two sites of different nature. It was found that the dye adsorption on chitin in type I and II sites differed in both the adsorption affinity and maximum adsorption capacity. Based on the dimensionless separation factor RL it was found that the dye adsorption mechanism in type I sites was an ion exchange, whereas in the case of type II sites it was a physical adsorption. A correlation was found between dye adsorption on chitin and the number of sulfone groups in a dye molecule. However, neither molecular weight nor the number of aromatic rings was correlated with dye adsorption.
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