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Reaktor

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Published by Universitas Diponegoro

ISSN : 08520798 EISSN : 24075973 DOI : https://doi.org/10.14710/reaktor.xx.x.xx-xx

Chemical Engineering, Chemistry & Bioengineering Control & Systems Engineering Energy Materials Science & Nanotechnology

Reaktor invites contributions of original and novel fundamental research. Reaktor publishes scientific study/ research papers, industrial problem solving related to Chemical Engineering field as well as review papers. The journal presents paper dealing with the topic related to Chemical Engineering including: Transport Phenomena and Chemical Engineering Operating Unit Chemical Reaction Technique, Chemical Kinetics, and Catalysis Designing, Modeling, and Process Optimization Energy and Conversion Technology Thermodynamics Process System Engineering and products Particulate and emulsion technologies Membrane Technology Material Development Food Technology and Bioprocess Waste Treatment Technology

Arjuna Subject : Teknik (semua kategori) - Teknik (Lain-Lain)

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Search results for , issue "Volume 12, Nomor 2, Desember 2008" : 10 Documents clear

PENGARUH KONSENTRASI KATALIS DAN PERBANDINGAN MOLARITAS REAKTAN PADA SINTESIS SENYAWA Galuh Widiyarti; Muhammad Hanafi
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

In the laboratory scale, the effect of the concentration of H2SO4 catalyst (1.25-6.25) (% w/w) and the equivalent mol ratio between lauric acid and glycerol (1:1; 1:2.5; 2.5:1) on the synthesis of a-monolaurin has been studied. The a-monolaurin compound has been synthesized from lauric acid and glycerol was done by batch esterification on the free solvent system. The esterification by using 5% H2SO4 catalyst and equivalent mol ratio between lauric acid and glycerol 1:2.5 produced most monolaurin, and dilaurin in amount of 31.14 and 4.42%, respectively. The monolaurin and dilaurin are identified by thin layer chromatography (TLC), infrared spectrophotometer (FTIR), liquid chromatography-mass spectrometer (LC-MS), and Nuclear Magnetic Resonance (NMR) spectrometer. The spectral data of monolaurin was compared to spectral data of standard a-monolaurin.Telah dilakukan penelitian sintesis senyawa a-monolaurin dari asam laurat dan gliserol, dengan konsentrasi katalis H2SO4 (1,25 s.d. 6,25) (% berat) dan perbandingan molaritas reaktan asam laurat terhadap gliserol (1:1; 1:2,5; dan 2,5:1) sebagai parameter. Pada reaksi esterifikasi dengan konsentrasi katalis H2SO4 5% dan perbandingan molaritas asam laurat terhadap gliserol 1:2,5 dihasilkan senyawa a-monolaurin terbanyak 31,14% sebagai hasil utama dan senyawa a,a’-dilaurin 4,42% sebagai hasil samping sintesis. Kedua senyawa hasil sintesis diidentifikasi dengan kromatografi lapis tipis (KLT), spektrofotometer infra merah (FTIR), spektrometer massa liquid chromatography-mass spectrometer (LC-MS), dan spektrometer resonansi magnetik inti (NMR). Karakteristik senyawa a-monolaurin hasil sintesis dibandingkan dengan karakteristik a-monolaurin standar.

EKSTRAKSI ASAM SITRAT DAN ASAM OKSALAT : PENGARUH TRIOCTYLAMINE SEBAGAI EXTRACTING POWER DALAM BERBAGAI SOLVEN CAMPURAN TERHADAP KOEFISIEN DISTRIBUSI Mega Kasmiyatun; Bakti Jos
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

Generally, liquid waste of citric acid industry containing a highly citric acid, oxalic acid, due to precipitation process of calcium citrate less completely. Liquid-liquid extraction process is this one alternative that used to recover citric acid and oxalic acid, either in the product separation process from the fermentor or the treatment of its liquid waste. In order to understand, that the extraction process can be applied both technically and economically, it needs a more study the extraction parameters. The investigation has carried out about study of the extraction of citric acid and oxalic acid used trioctyl-amine as extracting power on various mix solvent and its ratio, related to the distribution coefficient. Extraction used a separating funnel that it was shaked with using an automatic shaker, which adjusted on specific velocity during 2.5 hours. The rafinate and extract were separated by separating funnel, then they were analyzed both concentration of citric acid and oxalic acid using a high performance liquid chromatography (HPLC). The results of the research show that the mixed solvent (consist of 15% trioctyl amine, 70% dodecane, and 15% hexanol), for the extraction of citric acid produce both the highest distribution coefficient and percentage of separation were 1.15 and 74.22%, respectively; and this were achieved for the ratio between the solvent and diluent of 2.5:1. For the extraction of oxalic acid similar result were obtained, and the value were 3.78 and 88.31%, respectively, for the ratio between solvent and diluent of 2:1.Limbah cair pabrik asam sitrat pada umumnya mengandung asam sitrat, asam oksalat, cukup tinggi akibat proses pengendapan calsium sitrat yang kurang sempurna. Proses ekstraksi cair-cair adalah salah satu alternatif yang dapat digunakan untuk pengambilan kembali asam sitrat dan asam oksalat, baik pada proses pemisahan produk yang keluar dari fermentor maupun pada proses pengolahan limbah cairnya. Untuk mengetahui apakah proses ekstraksi dapat diterapkan secara teknis, maka perlu dilakukan pengkajian lebih mendalam parameter-parameter ekstraksi. Pada penelitian ini telah dilakukan pengkajian tentang ekstraksi asam sitrat dan asam oksalat dengan menggunakan trioctylamine sebagai extracting power pada bermacam solven campuran dan pada berbagai perbandingan, hubungannya dengan koefisien distribusinya. Ekstraksi pada berbagai kondisi rancangan percobaan dilakukan pada corong pemisah, yang penggojokannya dilakukan dengan bantuan automatic shaker yang di set pada kecepatan tertentu selama 2,5 jam. Rafinat dan ekstrak dipisahkan selanjutnya dianalisis kadar asam sitrat maupun asam oksalat dengan menggunakan HPLC. Hasil penelitian menunjukkan bahwa solven campuran (yang terdiri dari 15% trioctylamine, 70% dodecane dan 15% hexanol) menghasilkan koefisien distribusi dan persentase pemisahan solute berturut-turut untuk asam sitrat 1,15 dan 74,22% pada perbandingan solven dan diluen 2,5:1; sedang untuk ekstraksi asam oksalat sebesar 3,78 dan 88,31% pada perbandingan solven dan diluen 2:1.

PERANAN KATALIS TiO2/SiO2-MONTMORILLONIT PADA REAKSI KONVERSI SITRONELAL MENJADI ISOPULEGOL Is Fatimah; Dwiarso Rubiyanto; Torikul Huda
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

Catalytic conversion of citronellal to isopulegol over TiO2/SiO2-montmorillonite catalyst was studied for citronellal isolated from Cymbopogon leaf oil. The role of physico-chemical characteristics of montmorillonite and SiO2-montmorillonit catalyst on total conversion, activity and selectivity to produce isopulegol was studied. Activity test was conducted for citronellal cyclication for 4 hour. The total conversion, catalyst activity and catalyst selectivity to produce isopulegol were evaluated based on product composition obtained by GC-MS analysis. The experimental result showed that TiO2/SiO2-montmorillonite plays role in the increase of total conversion significantly from 87.80% over SiO2-montmorillonit and 85.38% over natural montmorillonite become 95.53%. Total conversion and selectivity of the catalyst to produce isopulegol increase could be related to Lewis acidity of TiO2/SiO2-montmorillonite, and also specific surface area enhancement. However, in the range of 1:1.25 to 1:5.0 catalyst to citronellal mass ratio, there was no influence on total conversion and selectivity to produce isopulegol. This may be caused by dominant influence of Lewis acidity compared to other physico-chemical characteristic of material. Kinetics study of the reaction showed that TiO2 dispersion on SiO2-montmorillonite almost doubles the reaction rate constant with the factor of 1.955. Konversi katalitik sitronelal menjadi isopulegol menggunakan katalis TiO2/SiO2-montmorillonit dipelajari terhadap sitronelal hasil isolasi minyak daun sereh. Peranan karakter fisikokimiawi material katalis montmorillonit alam dan SiO2-montmorillonit terhadap konversi total, aktivitas dan selektivitas dalam pembentukan isopulegol dipelajari. Uji aktivitas katalis dilakukan pada reaksi siklisasi sitronelal selama 4 jam. Konversi total, aktivitas katalis dan selektivitas terhadap isopulegol dihitung berdasar perubahan komposisi hasil reaksi yang ditentukan menggunakan GC-MS. Hasil penelitian menunjukkan bahwa katalis TiO2/SiO2-montmorillonit berperanan meningkatkan konversi total reaksi secara signifikan dari sebesar 87,80% pada penggunaan SiO2-montmorillonit dan 85,38% dengan menggunakan montmorillonit alam menjadi sebesar 95,53%. Peningkatan konversi total dan selektivitas terhadap isopulegol berkaitan dengan keasaman Lewis yang dimiliki oleh TiO2/SiO2-montmorillonit serta peningkatan luas permukaan spesifik material. Namun pada rentang perbandingan massa katalis terhadap sitronelal 1:1,25 hingga 1:5,0 tidak berpengaruh signifikan terhadap konversi total dan selektivitas produk isopulegol. Hal ini mungkin disebabkan peranan keasaman Lewis lebih dominan terhadap sifat-sifat fisikokimiawi material katalis. Studi kinetika reaksi menunjukkan bahwa dispersi TiO2 pada SiO2-montmorillonit meningkatkan konstanta laju reaksi dengan faktor sebesar 1,955.

THE INFLUENCES OF NATURAL GAS IMPURITIES TO THE SURFACE TENSION OF BLENDED PIPERAZINE-N-METHYLDIETHANOLAMINE (MDEA) SOLUTION Iwan Ratman; Ahmad Fauzi Ismail
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

This study focuses on the effect of impurities in the natural gas stream on the characteristic of surface tension in the blended piperazine and MDEA solution. Hydrocarbon liquids, Iron Sulphide, Sodium Chloride, Acetic Acid, Methanol and Polyethylene Glycol were used as the impurities. The results indicated that the type of impurities determined the surface tension changes of the amine solution. The concentration of piperazine-MDEA blends also enhanced to the increasing of surface tension. Iron sulphide, hydrocarbons and sodium chloride as the impurities in the amine solution were the most influential factors to the surface tension. Statistical experimental method was employed to determine the main effect in the increasing of surface tension. Full factorial design and response surface methodology (RSM) coupled with central composite design (CCD) were used to determine the increasing of surface tension in the amine solution. A central composite design was used to determine the main variables such as iron sulphide, hydrocarbon and sodium chloride. The maximum surface tension of 74.33 mNm-1 was determined at the combined impurities concentrations of Iron Sulphide at 6.346 ppm, Hydrocarbon liquids at 11.827 ppm and Sodium Chloride at 8.261 ppm.Pada penelitian ini difokuskan untuk mengetahui pengaruh impuritas didalam aliran gas alam terhadap karakteristik tegangan permukaannya pada campuran larutan MDEA-piperazin. Hidrokarbon, besi sulfida, NaCl, asam asetat, methanol dan PEG digunakan sebagai larutan impuritas pada gas alam. Pada penelitian ini menunjukan bahwa jenis dari impuritas akan mempengaruhi besarnya tegangan permukaan yang dihasilkan pada larutan amin. Konsentrasi larutan amin juga mempengaruhi tegangan permukaan yang dihasilkan. Besi sulfida, hidrokarbon dan NaCl adalah faktor penting yang menentukan besanya tegangan permukaan yang dihasilkan. Metode statistik yang menggunakan response surface methodology (RSM) yang digabungkan dengan central composite design (CCD) telah digunakan untuk mengetahui faktor utama yang menentukan tegangan permukaan. Tegangan permukaan yang paling tinggi dihasilkan pada konsentrasi besi sulfida 6,346 ppm, hidrokarbon 11,827 ppm dan NaCl 8,261 ppm adalah sebesar 74,33 mNm-1.

DIRECT ETHOXYLATION OF GLYCEROL MONO OLEATE FROM PALM OIL DERIVATE AS A NOVEL NON-IONIC POLYMERIC SURFACTANT Joddy Arya Laksmono; Indri Badria Adilina; Egi Agustian
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

The work investigates ethoxylation of glycerol mono oleate (GMO) performed in the presence of an alkaline catalyst. Glycerol mono oleate applied was derivated from Indonesian palm oil. The reaction was conducted with variation of Glycerol mono oleate : ethylene oxide ratio, temperature, and catalyst concentration. Forier Transform Infra Red (FTIR) and Nuclear Magnetic Resonance (NMR) analysis showed products with degrees of ethoxylation n=2 and n=3. FTIR analysis of products gave a new peak at 1570 cm-1 supporting that C-O-C bond was formed. New peaks were also observed in 13-C-NMR analysis of run 2 and run 3 with chemical shift of (δ) 61.3385; 61.9108; 62.5117; 63.8566; 66.0982; 72.6127 and 61.2172; 63.2393; 65.9100; 72.5201, respectively. Glycerol mono oleate ethoxylated was yielded and could be useful for a novel non-ionic polymeric surfactant.

THE EFFECT OF TYPE ZEOLITE ON THE GAS TRANSPORT PROPERTIES OF POLYIMIDE-BASED MIXED MATRIX MEMBRANES Tutuk Djoko Kusworo; Ahmad Fauzi Ismail; Azeman Mustafa; Kang Li
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

The permeation rates of O2, N2, CO2 and CH4 has been studied for polyimide-polyethersulfone (PI/PES) blends-zeolite mixed matrix membranes synthesized in our laboratory. The study investigated the effect of zeolite loading and different zeolite type on the gas separation performance of these mixed matrix membranes. Frequency shifts and absorption intensity changes in the FTIR spectra of the PI/PES blends as compared with those of the pure polymers indicate that there is a mixing of polymer blends at the molecular level. Differential scanning calorimetry measurements of pure and PI/PES blends membranes have showed one unique glass transition temperature that supports the miscible character of the PI/PES mixture. The PI/PES-zeolite 4A mixed matrix membrane with 25 wt % zeolite loading produced the highest O2/N2 and CO2/CH4 selectivity of around 7.45 and 46.05, respectively.

CONVERSION OF PINEAPPLE JUICE WASTE INTO LACTIC ACID IN BATCH AND FED – BATCH FERMENTATION SYSTEMS Abdullah Mochamad Busairi
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

Pineapple juice waste contains valuable components, which are mainly sucrose, glucose, and fructose. Recently, lactic acid has been considered to be an important raw material for the production of biodegradable lactide polymer. The fermentation experiments were carried out in a 3 litres fermentor (Biostat B Model) under anaerobic condition with stirring speed of 50 rpm, temperature at 40oC, and pH of 6.00. Effect of feed concentration on lactic acid production, bacterial growth, substrate utilisation and productivity was studied. The results obtained from fed- batch culture fermentation showed that the maximum lactic acid productivity was 0.44 g/L.h for feed concentration of 90 g/L at 48 hours. Whereas the lactic acid productivity obtained from fed-batch culture was twice and half fold higher than that of batch culture productivity. Buangan jus nanas mengandung komponen yang berharga terutama sukrosa, glukosa, dan fruktosa. Asam laktat adalah bahan baku yang terbaru dan penting untuk dibuat sebagai polimer laktat yang dapat terdegradasi oleh lingkungan. Percobaan dilakukan pada fermentor 3 liter (Model Biostat B) di bawah kondisi anaerob dengan kecepatan pengadukan 50 rpm, temperatur 40oC, dan pH 6,00. Pengaruh konsentrasi umpan terhadap produksi asam laktat, pertumbuhan mikroba, pengggunaan substrat dan produktivitas telah dipelajari. Hasil yang didapatkan pada fermentasi dengan menggunakan sistem fed-batch menunjukkan bahwa produktivitas asam laktat maksimum adalah 0.44 g/L,jam dengan konsentrasi umpan, 90 g/L pada waktu 48 jam. Bahkan produktivitas asam laktat yang didapat pada kultur fed-batch lebih tinggi 2,5 kali dari pada proses menggunakan sistem batch

ALGORITMA MODULAR UNTUK SISTEM PROSES DENGAN RECYCLE - KEADAAN TUNAK PADA PERANGKAT LUNAK BEBAS BIAYA LISENSI Setia Budi Sasongko
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

Computer simulasion can be developed to comprehend a system process characteristic and can be used to train the operator of process. The first problem of programming is high price of the licence. Using the FOC (free of charge) software solve of the previous problem such as Scilab and Open Office which comparable with Matlab and Excel. The objectives of this article develop process system programming which has recycle system and user friendly programming. Modular algorithm programming is introduced to solve recycle process system. Graphical User Interface (GUI) also introduces to make user friendly programming. Execution of the program performs stable and correct results.

REAKSI KATALITIS ESTERIFIKASI ASAM OLEAT DAN METANOL MENJADI BIODIESEL DENGAN METODE DISTILASI REAKTIF Kusmiyati Kusmiyati
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

Biodiesel is an alternative diesel fuel that is produced from vegetable oils and animal fats. Generally, it is formed by trans etherification reaction of triglycerides in the vegetable oil or animal fat with an alcohol. In this work, etherification reaction was carried out using oleic acid, methanol and sulphuric acid as a catalyst by reactive distillation method. In order to determine the best conditions for biodiesel production by reactive distillation, the experiments were carried out at different temperature (1000C, 1200C, 1500C and 1800C) using methanol/oleic acid molar ratios (1:1, 5:1, 6:1, 7:1, 8:1), catalyst/ oleic acid molar ratios (0.5%wt, 1%wt, 1.5%wt and 2%wt) and reaction times (15, 30, 45, 60, 75 and 90 minutes). Result show that at temperature 1800C, methanol/oleic acid molar ratio of 8:1, amount of catalyst 1% for 90 minute reaction time gives the highest conversion of oleic acid above 0.9581. Biodiesel product from oleic acid was analyzed by ASTM (American Standard for Testing Material). The results show that the biodiesel produced has the quality required to be a diesel substitute. Biodiesel merupakan salah satu bahan bakar alternatif pengganti bahan bakar fosil yang diproduksi dari bahan baku minyak nabati dan lemak hewan. Secara umum biodiesel diproduksi melalui reaksi transesterifikasi minyak nabati atau lemak hewan dan alkohol. Pada penelitian ini proses esterifikasi pada pembuatan biodiesel menggunakan bahan baku asam oleat murni (99%), metanol dan katalis asam sulfat dengan metode distilasi reaktif. Distilasi reaktif merupakan penggabungan antara proses reaksi dan proses pemisahan dalam satu unit proses sehingga memungkinkan diperoleh biodiesel dengan kemurnian yang tinggi. Variabel yang dipelajari pada penelitian ini adalah temperatur (1000C, 1200C, 1500C, 1800C), jumlah katalis H2SO4 (0,5% berat, 1% berat, 1,5% berat, 2% berat), rasio metanol : asam oleat dinyatakan 1:1, 5:1, 6:1, 7:1, 8:1 (dalam % berat) terhadap konversi asam oleat serta. Berdasarkan hasil penelitian, konversi maksimum yang dapat dicapai sebesar 0,9581 pada kondisi reaksi berat katalis H2SO4 1% berat, rasio metanol:asam oleat 8:1 dan suhu reaksi 1800C. Berdasarkan hasil analisa ASTM, biodiesel yang diperoleh memenuhi standar bahan bakar cair dan dapat digunakan sebagai bahan bakar pengganti petroleum diesel.

PEMUTIHAN PULP DENGAN HIDROGEN PEROKSIDA Ahmad M. Fuadi; Hari Sulistya
Reaktor Volume 12, Nomor 2, Desember 2008
Publisher : Dept. of Chemical Engineering, Diponegoro University

The use of bleaching agent has increased as the result of increasing of paper consumption. The conventional bleaching agent that commonly used is material containing of chlorine. This material is not environmentally friendly and should be replaced by environmentally benign chemical, such as H2O2. About 40 gram of dry Akasia pulp was mixed with 600 ml of distilled water was put into plastic bag heated in a water bath. When the temperature reached 630C, a solution of 4 % of H2O2 and distilled water was added to obtain 5 % consistency. This mixture was put into water bath and was heated for 2 hours. The same procedure was conducted with various concentration of H2O2, time and pH. At the end of the process, the pulp was dewatered and washed. The filtrate obtained from the initial dewatering was used to determine the residual of H2O2. The pulp was analyzed to determine brightness, fiber strength and kappa number. The maximum achievement of brightness was 62,1 % ISO, 6.86 of kappa number and 1.02 kg/15 mm of fiber strength, which are reached at16 % of the use of H2O2, pH 11 and 5 hours of bleaching time. This achievement is similar to bleaching result by the additional of 4% H2O2. Inefficient usage of H2O2 was caused by some metal ions in the pulp which facilitate the decomposition of H2O2 to produce oxygen and water which has not effect on increasing the brightness. To improve the bleach ability of H2O2, initial treatment to remove metal ions from pulp should be done. Seiring dengan meningkatnya kebutuhan kertas, kebutuhan bahan pemutih juga mengalami kenaikan. Saat ini bahan pemutih yang banyak digunakan adalah senyawa yang mengandung khlor. Senyawa ini sangat tidak ramah lingkungan, oleh karena itu, perlu dicari bahan yang ramah lingkungan untuk menggantikannya. Salah satunya adalah hidrogen peroksida. Pulp dari pohon akasia sebanyak 40 gram kering dicampur dengan 600 ml aquadest dimasukkan dalam kantung plastik dipanaskan dalam water bath. Setelah suhu mencapai 630C, kantung plastik diambil kemudian ditambah hidrogen peroksida sebanyak 4% dari pulp kering dan aquadest sehingga mencapai konsistensi 5%. Campuran dimasukkan kedalam water bath untuk dipanaskan lebih lanjut hingga 2 jam. Hal yang sama dilakukan pada berbagai kadar hidrogen peroksida, waktu dan pH. Pada akhir proses, pulp dipisahkan dengan filtratnya dan dicuci dengan aquades. Filtrat yang diperoleh dianalisa sisa hidrogen peroksidanya. Pulp yang diperoleh dianalisa derajat putih, kekuatan serat serta bilangan kappanya. Maksimum derajat putih yang bisa dicapai adalah 62,1% ISO, bilangan kappa 6,86 dan fiber strength 1,02 kg/15mm yang dicapai pada pemakaian H2O2 16%, pH 11 selama 5 jam. Pencapaian ini hampir sama dengan hasil yang dicapai ketika penambahan H2O2 4%. Ketidak efektifan pemakaian H2O2 disini disebabkan oleh adanya beberapa metal ion yang ada di dalam pulp yang bertindak sebagai katalisator terjadinya reaksi dekomposisi dari H2O2 membentuk oksigen dan air yang tidak efektif dalam memberikan efek terhadap proses pemutihan. Untuk meningkatkan bleach ability dari hydrogen peroksida, perlu dilakukan treatment awal untuk mengeluarkan metal ion dari pulp.

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Editorial Address Department of Chemical Engineering, Diponegoro University Jl. Prof. Soedarto SH Tembalang Semarang 50275

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Contact Name
Dessy Ariyanti

Contact Email
dessy.ariyanti@che.undip.ac.id

Phone
+62247460058

Journal Mail Official
j.reaktor@che.undip.ac.id

Editorial Address
Department of Chemical Engineering, Diponegoro University Jl. Prof. Soedarto SH Tembalang Semarang 50275

Location
Kota semarang,

Jawa tengah

INDONESIA