Indriana Kartini
Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, Indonesia

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Preparation of Water Repellent Layer on Glass Using Hydrophobic Compound Modified Rice Hull Ash Silica Alfa Akustia Widati; Nuryono Nuryono; Dessy Puspa Aryanti; Madjid Arie Wibowo; Eko Sri Kunarti; Indriana Kartini; Bambang Rusdiarso
Indonesian Journal of Chemistry Vol 18, No 4 (2018)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (375.252 KB) | DOI: 10.22146/ijc.26714

Abstract

In this study water repellent layered glass has been prepared by coating silica (SiO2) combined with a hydrophobic silane compound. SiO2 was extracted from rice hull ash and two silane compounds, namely hexadecyltrimethoxysilane (HDTMS) and trimethylchlorosilane (TMCS) were used. Coating was performed through two deposition techniques, i.e. one step (mono-layer) and layer by layer (LBL, multi-layer). The effect of silane to SiO2 mole ratio, silane type and layer number on the glass characters was evaluated. Characterization included hydrophobicity, transparency, surface roughness and stability of coating. Results showed that increasing the mole ratio of silane to SiO2 and the layer number increased the hydrophobicity of the glass surface. The optimum mole ratio was 5:1 and the significant increase of contact angle occurred at lower mole ratio, but the stability tends to be increased at higher mole ratio. For HDTMS-SiO2 layer, the technique of LBL technique produced a coating with higher hydrophobicity and transparency than single-stage one. The LBL technique produced the highest water contact angle of 103.7° with transmittance of 96%, while for TMCS-SiO2 layer the one stage technique produced hydrophobic layer with higher water contact angle of 108.0° and transparency about 94.52%. The prepared hydrophobic glasses were relatively stable in polar and non-polar solvents, but unstable to ambient conditions.
Short Time Synthesis of Titania Nanotubes: Effect of Pre-Mixing Prior Hydrothermal Indriana Kartini; Ira Nur Arba’atul Jannah; Fitri Rizki Amalia; Salim Mustofa; Eko Sri Kunarti; Respati Tri Swasono
Indonesian Journal of Chemistry Vol 19, No 1 (2019)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (19.78 KB) | DOI: 10.22146/ijc.26777

Abstract

The effect of pre-mixing by mechanical stirring before hydrothermal and hydrothermal time on the crystalline phases and morphology of titania has been studied. It was shown that nanotubes titania can be obtained after 5 h hydrothermal at 150 °C. The XRD patterns and Raman spectra of the produced powders showed the existence of anatase and titanate crystalline phases. At the longest stirring, TiO2 (B) was observed. High textural coefficient for [200] plane of anatase (TC200) confirmed oriented growth of one-dimensional anatase along [200]. All powders resulted at various stirring time were nanotubes, as confirmed by Transmission Electron Microscope (TEM). It was found that the longer the stirring, the higher the surface area of the nanotubes. All powders showed type-IV isotherm for nitrogen gas adsorption/desorption, indicating the existence of mesoporous materials. However, long hydrothermal induced the nanospheres formation, hence reducing the surface area. The band-gap of the resulted titania nanotubes were ranging from 3.11–3.16 eV. The photocatalytic performance toward the degradation of methylene blue of the titania nanotubes was higher (~50%) compared to the bulk TiO2 (~5%) under visible-light and was comparable under UV-light (~60%). These results pave a way of producing visible-sensitive TiO2 photocatalyst by altering the morphology.
Synthesis and Photoactivity of Fe3O4/TiO2-Co as a Magnetically Separable Visible Light Responsive Photocatalyst Eko Sri Kunarti; Indriana Kartini; Akhmad Syoufian; Karolina Martha Widyandari
Indonesian Journal of Chemistry Vol 18, No 3 (2018)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (462.766 KB) | DOI: 10.22146/ijc.26831

Abstract

Synthesis of magnetic photocatalyst, Fe3O4/TiO2-Co, with characterization and photoactivity examination have been conducted. The synthesis was initiated by preparation of Fe3O4 particles using coprecipitation method. The Fe3O4 particles were then coated with TiO2-Co at a various ratio of Fe3O4:TiO2 and concentration of Co(II) dopant. The Fe3O4/TiO2-Co was characterized by FTIR, XRD, TEM, SEM-EDX, VSM, and SR UV-visible methods. Photoactivity of the Fe3O4/TiO2-Co was carried out using methylene blue as a target molecule in degradation reaction within a batch system. By using optimum conditions, the degradation of methylene blue solution was performed under exposure to UV, visible light and dark condition. Results showed that the Fe3O4/TiO2-Co formation was confirmed by the presence of Fe3O4 and anatase diffraction peaks in the X-ray diffractogram. SR UV-Vis spectra indicated that the Fe3O4/TiO2-Co was responsive to visible light. Band gap energy of the Fe3O4/TiO2-Co with dopant concentration of 1; 5; 10 and 15% were 3.22; 3.12; 3.09 and 2.81 eV, respectively. The methylene blue solution can be well photodegraded at a pH of 10 for 210 min. The Fe3O4/TiO2-Co has the highest ability to methylene blue photodegradation with dopant concentration of 10% gave degradation yield of 80.51 and 95.38% under UV and visible irradiation, respectively.
Synthesis of Mesoporous Silica from Beach Sand by Sol-Gel Method as a Ni Supported Catalyst for Hydrocracking of Waste Cooking Oil Siti Salamah; Wega Trisunaryanti; Indriana Kartini; Suryo Purwono
Indonesian Journal of Chemistry Vol 22, No 3 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.70415

Abstract

Mesoporous silica (MS) supported by nickel was synthesized from Parangtritis beach sand and assessed for its activity and selectivity as catalysts in hydrocracking waste cooking oil into biofuel. The synthesis of MS was done by the sol-gel method. Ni/MS catalysts using Ni weight variations of 1, 5, and 10 wt.% were denoted as Ni/MS1, Ni/MS5, and Ni/MS10 and were compared to standard mesoporous silica (Ni/SBA-15). The catalysts were characterized using FTIR, XRD analysis, N2 gas sorption analysis, SEM-EDX, and TEM. Catalyst Ni/MS1, Ni/MS5, Ni/MS10, and Ni/SBA-15 have specific surface areas of 130.5, 195.9, 203.9, and 381.2 m2/g and the average pores of 12.30, 9.80, 11.12, and 8.70 nm, respectively. The hydrocracking was run four times to evaluate the catalyst reusability. The hydrocracking WCO has 95.8, 82.4, and 85.2%, respectively. While Liquid fractions produced were 38.8, 43.2, and 50.2 wt.%, each of which contains gasoline of 37.09, 39.76, and 44.27 wt.%, Ni/MS10 has the highest liquid products of 50.2 wt.% and was selective to gasoline fractions up to 44.27%. Therefore, the catalyst synthesized from Parangtritis beach sand is selective for gasoline-fraction hydrocarbon and has hydrocracking activity up to 4 runnings.
Synthesis of Zeolite/NPK Coated with Cu-Alginate-PVA-Glutaraldehyde as a Slow-Release Fertilizer Ratna Betriani; Sutarno Sutarno; Indriana Kartini; Jolang Budiarta
Indonesian Journal of Chemistry Vol 23, No 1 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.76205

Abstract

The objectives of this study were to synthesize zeolite/NPK coated with Cu-alginate-PVA-glutaraldehyde as a material for slow-release fertilizers and to study the effect of various Cu concentrations in the coating material on the resistance of the zeolite/NPK fertilizer and to study the release rate reaction in citric acid. The study began with the synthesis of the zeolite/NPK fertilizer and the Cu-alginate-PVA-glutaraldehyde coating materials with variations of Cu concentration of 0.0; 0.2; 0.4; 0.6; 0.8; and 1.0 M. The Zeolite/NPK fertilizer and the coated NPK fertilizer were characterized by XRD and FTIR. The determination of the released N and P was conducted using a UV-Visible spectrophotometer, while released K and Cu was analyzed using AAS. XRD showed that the composite had a crystalline structure. The FTIR spectra showed characteristic cross-linking interactions between PVA-glutaraldehyde and Cu-alginate. A study of the release kinetics of zeolite/NPK coated with Cu-alginate-PVA-glutaraldehyde showed that increasing Cu concentration to 0.4 M decreased the amount of nutrition released, and the release process followed the pseudo-second-order kinetics. The release rate constants of N,P,K and Cu in the citric acid medium on zeolite/NPK coated with Cu 0.4 M were 8.49 × 10−3, 17.48 × 10−3, 21.73 × 10−3, and 8.57 × 10−3 mg g−1 h−1, respectively.