Tutik Dwi Wahyuningsih

THE ADSORPTION OF Pb(II) AND Cr(III) BY POLYPROPYLCALIX[4]ARENE POLYMER

A research has been conducted to investigate the adsorption behavior of Pb(II) and Cr(III) onto polypropylcalix[4]arene polymer. The polypropylcalix[4]arene polymer was synthesized in the presence of H2SO4 catalyst and chloroform under N2 condition for 5 h using 25-allyloxy-26,27,28-trihydroxycalyx[4]arene as the precursor. The Polymer was obtained as yellow crystal with melting point of 288-290 °C and its relative molecular weight was 44.810 g.mol. The application of polypropylcalix[4]arene for trapping heavy metal cations and its adsorption model were examined by stirring the suspension of the calixarene in the sample solutions for various pH, time, and concentration of Pb(II) and Cr(III) solution. Effect of pH on batch experiments for the mentioned ions indicated that the optimum pH for metal binding were 5 for lead(II) and chromium(III). The adsorption model of metal ions on polypropylcalix[4]arene followed both the pseudo second order adsorption of Ho’s and Langmuir isotherm adsorption kinetics models with rate constant (k) were 6.81 x 10 min for Pb(II) and 2.64 x 10 min for Cr(III). The adsorption equilibrium constant, K, were 5.84 x 10 L.mol for Pb(II) and 4.66 x 10 L.mol for Cr(III). The maximum adsorption capacity of polypropylcalix[4]arene to Pb(II) and Cr(III) were 16.31 and 18.14 mg.g with adsorption energy of 32.90 and 32.34 kJ.mol, respectively.

Green synthesis of some novel dioxolane compounds from Indonesian essential oils as potential biogreases

Greases are mostly prepared from petroleum base stocks that make it toxic to the environment. The demand for green greases has led to in depth research of other renewable resources. Vegetable oils are promising candidates due to their renewability and low toxicity. However, it has poor oxidation stability and high total acid number. One way to solve this problem is chemical modification of its fatty acid structure. We report some novel dioxolane compounds from oleic acid and benzaldehyde derivates from some Indonesian essential oils via several steps, i.e: hydroxylation, esterification and acetalization. The esterification and acetalization reaction was carried out by green procedure using sonochemical method and montmorillonite KSF as a catalyst. Hydroxylation of Oleic acid was performed by KMnO4 to give 9,10-dihydroxyoctadecanoic (DHOA) in 47% yield. The esterification was done using methanol yielded methyl 9,10-dihydroxyoctadecanoate (MDHO) as white powder in 94%. Acetalization of the ester MDO with va...

Synthesis and characterization of novel benzohydrazide as potential antibacterial agents from natural product vanillin and wintergreen oil

A chalcone-like benzohydrazide derivatives (3) has been synthesis from natural resources vanillin (1a) and wintergreen oil (1b). This compound was synthesis as modified natural resource antibacterial agent. Some modification was done to increase the biological activity. Bromide was introduced to the vanillin structure to increase the activity (2a), whereas Hydrazine monohydrate was reacted with wintergreen oil to make new nucleophile (2b). Furthermore, chalcone like benzohydrazide compound was synthesized by stirring 5-bromovanillin (2a) with salicyl hydrazine (2b) at room temperature for 2-3 hours. The product was analyzed by FTIR, GCMS, 1H- and 13C-NMR to confirm its structure. The result showed that 5-bromovanillin, salicyl hydrazine, and benzohydrazide were successfully synthesized with 98, 78, and 33% of yield respectively. The target molecule 3 achieved with yellowish color with m.p. 106-111 °C, 97% purity.

Synthesis and Antibacterial Activities of N-Phenylpyrazolines from Veratraldehyde

Some novel N-phenylpyrazolines were synthesized and investigated for their antibacterial activitiy. Chalcones 2-4 which were prepared from acetophenone and veratraldehyde derivatives were reacted with phenylhydrazine to give N-phenylpyrazolines 5-7. All of the synthesized compounds were characterized using FTIR, GC-MS, and NMR spectrometers. Further, antibacterial activity of N-phenylpyrazolines were evaluated by agar well-diffusion method against Staphylococcus aureus, Bacillus cereus, Bacillus subtilis, Escherichia coli, and Shigella flexneri. The highest activity (highest inhibition zone) of compound 5 was 2.6 mm (at 1000 ppm) against B. subtillis, compound 6 was 7.25 mm (at 1000 ppm) against S. aureus, and compound 7 was 6.75 mm (at 500 ppm) against S. aureus. The results indicated that compound 6 and 7 exhibited promising antibacterial activity.

Green synthesis of chalcones derivatives as intermediate of flavones and their antibacterial activities

Four chalcones derivatives have been synthesized from 3,4-dimethoxybenzaldehyde and acetophenone derivatives (2-hydroxy acetophenone, 2,4-dihydroxy acetophenone, 2,5-dihydroxy acetophenone and 2,6-dihydroxy acetophenone). The synthesis of these chalcones were conducted by Claisen-Schmidt condensation using grinding techniques at room temperature in the absence of solvents. The chalcones were prepared by grinding together equivalent amount of the approriate hydroxyacetophenone and 3,4-dimethoxybenzaldehyde in the presence of solid sodium hydroxide. Grinding techniques for synthesis of the chalcones derivatives is simple, efficient and environmentally benign compared to conventional methods. Then, the four chalcones derivatives undergo cyclization reactions to produce four flavones after reacted with iodine. The synthesized compounds were characterized by spectrometry (IR, 1H-NMR, 13C-NMR and MS).