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Reaktor
Published by Universitas Diponegoro
ISSN : 08520798     EISSN : 24075973     DOI : https://doi.org/10.14710/reaktor.xx.x.xx-xx
Core Subject : Science, Engineering,
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)
Articles 9 Documents
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Search results for , issue "Volume 15, No.2, OKTOBER 2014" : 9 Documents clear
UKURAN PARTIKEL DAN KONFORMASI KRISTAL ZEOLIT-A HASIL SINTESIS DENGAN PENAMBAHAN TETRAPROPILAMMONIUM HIDROKSIDA (TPAOH) Nurul Widiastuti; Farhanah Thalib; Didik Prasetyoko; Hamzah Fansuri
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (684.131 KB) | DOI: 10.14710/reaktor.15.2.132-138

Abstract

Abstract PARTICLE SIZE AND CRYSTAL CONFORMATION OF SYNTHESIZED ZEOLITE-A WITH TETRAPROPYLAMMONIUM HYDROXIDE (TPAOH) ADDITION. The aims of this research is to study the effect of tetrapropylammonium hydroxide (TPAOH) concentration in the synthesis of zeolite A to its physical characteristics such as crystallinity, crystal conformation and average crystal size. The zeolite A was synthesized with composition 3.165 Na2O : 1.000 Al2O3: 1.926 SiO2: 128 H2O : x TPAOH where x was 0; 0.0385; 0.0577; 0.0770; 0.1540 and 4.1602. The zeolite was crystalized under hydrothermal condition in a stainless steel autoclave at 100°C for 5 hours. The resulting crystal was washed with distilled water until pH 8 and then dried in an oven at 80oC for 24 hours. FT-IR and XRD analysis results show that the synthesized zeolite A at x = 4.1602 has the lowest crystallinity. It is estimated due to the mass of TPAOH was four times higger than the mass of zeolite framework components (Si and Al). SEM and PSD (Particle Size Distribution) analysis results show that TPAOH concentration affected the crystal conformation and the average size of zeolite A particles. The formation of chained crystal conformation was caused by the electrostatic interactions between TPA+ and negatively charge of zeolite framework. In addition, the particel size of the synthesized zeolite A at x = 0.1540 was 2.024 µm which was smaller than the particel size of the synthesized zeolite A without TPAOH, which was 3.534 µm.  Keywords: average size of particles; crystal conformation; TPAOH; zeolite A  Abstrak Penelitian ini bertujuan untuk mempelajari pengaruh konsentrasi TPAOH (Tetrapropilamonium hidroksida) dalam sintesis zeolit A terhadap sifat fisikanya yang meliputi kekristalan, konformasi kristal dan ukuran rata-rata kristal yang terbentuk. Pada penelitian   ini   zeolit A   disintesis    dengan komposisi 3,165 Na2O : 1 Al2O3 : 1,926 SiO2 :128 H2O: x TPAOH. Konsentrasi TPAOH divariasikan dengan nilai x adalah 0; 0,0385; 0,0577; 0,0770; 0,1540 dan 4,1602. Metode hidrotermal digunakan dalam penelitian ini dengan kondisi suhu  hidrotermal 100°C dan waktu kristalisasi selama 5 jam dengan pH pencucian 8. Hasil karakterisasi menggunakan FT-IR (Fourier Transform – Infrared Spectroscopy) dan XRD (X-Ray Diffraction)  menunjukkan bahwa zeolit A yang disintesis dengan x = 4,1602 memiliki kekristalan terendah. Hal ini diperkirakan terjadi karena masa TPAOH yang digunakan empat kali lebih besar daripada masa penyusun zeolit (Si dan Al). Berdasarkan hasil karakterisasi menggunakan SEM (Scanning Electron Microscopy) dan PSD (Particle Size Distribution), dapat diketahui bahwa TPAOH berpengaruh terhadap konformasi kristal dan rata-rata ukuran kristalnya.  Terbentuknya konformasi kristal seperti rantai disebabkan oleh adanya interaksi elektrostatik antara muatan positif pada TPA+ dan muatan negatif dari kerangka zeolit. Zeolit A yang disintesis dengan x = 0,1540 memiliki ukuran partikel rata-rata 2,024 µm yang lebih kecil dari daripada zeolit A tanpa TPAOH yaitu sebesar 3,534 µm. Kata kunci : ukuran partakel rata-rata; konformasi kristal; TPAOH; zeolite A  
PENGOLAHAN PRIMER LIMBAH TEKSTIL DENGAN ELEKTROKOAGULASI Lieke Riadi; Whenny Ferydhiwati; Liok Dimas Sanjaya Loeman
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (402.993 KB) | DOI: 10.14710/reaktor.15.2.73-78

Abstract

Limbah industri tekstil di area pinggir kota Surabaya mempunyai karakteristik perbandingan COD dan BOD = 5.57. Limbah jenis ini sulit untuk dibiodegradasi. Studi ini mempelajari tekonologi elektrokoagulasi untuk mengolah limbah tekstil dengan menurunkan intensitas warna, Total Suspended Solid (TSS) dan Chemical Oxygen Demand (COD). Percobaan batch pada suhu kamar dilakukan untuk mempelajari pengaruh pH, jarak elektroda terhadap penurunan warna,TSS dan COD dan membandingkan biaya operasinya jika menggunakan pengolahan kimia.Effisiensi penurunan tertinggi untuk warna (91.96%),  TSS (49.17%), dan COD (29.67%) terjadi pada pH awal 4.0 dan jarak elektroda 2 cm dengan  elektroda Al/Al. Waktu optimum penurunan intensitas warna dalah 10 menit. Laju penurunan COD adalah : -dC/dt = 0.0053 C +0.056 , dengan C adalah konsentrasi COD. Jumlah sludge yang dihasilkan daripengolahan elektrokoagulasi  3.4 % lebih kecil dibandingkan menggunakan bahan kimia. Biaya yang digunakan untuk pengolahan dengan elektrokoagulasi 52.35 % lebih murah dibandingkan jika menggunakan koagulasi dengan bahan kimia ( tawas). Kata kunci : elektrokoagulasi, penurunan warna, penurunan TSS, laju degradasi COD, imbah tekstil Abstract Waste water from textile industry which is located in one suburb of Surabaya city as characteristic which the ratio of COD to BOD was 5.57. This type of waste water is difficult to be biodegraded. This study investigated elektrokoagulasi technology to treat textile waste water by removing color, total suspended solid, and Chemical Oxygen Demand. Batch experiment at room temperature was carried out to study the effect of pH, electrode distance for color, TSS and COD removal. This study also tried to compare the operation cost between elektrokoagulasi and chemical processes. The best removal efficiencies by Al electrodes was 91.96 % for color, 49.17 % for TSS and 29.67 % for COD which were under initial pH 4.0 and electrodes distance 2 cm. The optimum operation time for color removal was  found 10 minutes.The COD degradation rate was - dC/dt = 0.0053 C +0.056, with C= COD concentration. Sludge result from elektrokoagulasi was 3.4 % less than that by chemical treatment.The operation cost for elektrokoagulasi is 52.35 % less than that for chemical coagulation. 
Produksi Bioetanol dari Bahan Baku Singkong, Jagung dan Iles-iles :Pengaruh Suhu Fermentasi dan Berat Yeast Saccharomyces cerevisiae K. Kusmiyati; Lukhi Mulia Shitophyta
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (389.872 KB) | DOI: 10.14710/reaktor.15.2.97-103

Abstract

Kebutuhan bahan bakar di masa sekarang semakin bertambah besar sehingga berdampak pada menipisnya sumber bahan bakar dan meningkatnya polusi udara di lingkungan. Penggunaan bahan bakar alternatif dari sumber non fosil merupakan pilihan terbaik sebagai pengganti bahan bakar fosil. Bioetanol merupakan salah satu energi alternatif yang tepat digunakan baik di masa sekarang ataupun di masa yang akan datang. Bahan baku etanol yang digunakan pada penelitian ini adalah singkong, dan iles-iles.Variabel penelitian yang diamati temperatur fermentasi (30°C; 40°C;­­ 50°C) dan komposisi Saccharomyces cerevisiae (2,5 g; 5 g; 10 g; 15 g) Proses pembuatan bioetanol terdiri dari hidrolisis enzim yaitun likuifikasi menggunakan a-amylase1,6% v/w (t = 1 jam; T = 95-100°C; pH 6) dan sakarifikasi menggunakan b-amylase 3,2% v/w (t = 4 jam; T = 60°C; pH 5) serta proses fermentasi menggunakan Saccharomyces cerevisiae ( t = 120 jam; pH 4,5; yeast 5 g). Kadar etanol tertinggi dihasilkan pada temperatur fermentasi 30°C untuk semua bahan baku dengan kadar etanol masing-masing 83,43 g/L untuk singkong,80,77 g/L untuk jagung,dan 79,94 g/L untuk iles-iles.
SIFAT POLIMER DAN KEMAMPUAN TERBIODEGRADASI BLEND BIODEGRADABLE POLYMER POLI (L-ASAM LAKTAT) (PLLA) Johnner P Sitompul; Rizki Insyani; Hyung Woo Lee
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (349.521 KB) | DOI: 10.14710/reaktor.15.2.79-86

Abstract

 Poly(D,L-lactic acid) (PDLLA) and poly(ethylene glycol) (PEG) was used to modify mechanical and biodegradability properties of poly(L-lactic acid) (PLLA) through solution blending method using solvent mixture of dichloromethane-ethanol. Polymer samples were then characterized using FTIR, DSC, UTM, and enzymatic degradation test. FTIR spectrum of pure PLLA showed specific IR absorption peaks at wavenumber of 3504 cm-1 (-OH), 1757 cm-1 (-C=O), and 1381 cm-1 (-CH3 symmetric). Further, polymer blend samples showed absorption peak shifts at 1755 cm-1 and 1382 cm-1 for PLLA/PDLLA due to stereocomplex interaction and at 3429 cm-1 due to hydrogen bond interaction. DSC results showed that there was melting temperature depression for all polymer blend samples compared to pure PLLA with increasing of either PDLLA or PEG composition. In PLLA/PDLLA, two melting points were discovered because of homocrystallite and stereocomplex phase formation. While PLLA/PEG samples showed increasing crystallinity to 69% at 20%-wt PEG composition. Mechanical analysis showed that 10%-wt of PDLLA addition in PLLA produced better mechanical performance than pure PLLA while 20%-wt of PEG addition showed highest elongation at break with the value of 89%. Polymer blend samples were degradable during enzymatic degradation test represented by percent weight loss with maximum value of 21% for PLLA/PEG sample. Keywords: polymer properties, solution-blending, Poly(lactic acid), polymer blend, enzymatic degradation
FORTIFIKASI INORGANIK ZINK PADA TEPUNG UBI JALAR UNGU SEBAGAI BAHAN BAKU BUBUR BAYI INSTAN Noer Abyor Handayani; Herry Santosa; Bunga Profegama; Aditya Yuna
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (391.042 KB) | DOI: 10.14710/reaktor.15.2.111-116

Abstract

Fortifikasi zink pada bubur instan bayi berbahan dasar tepung ubi jalar ungu diharapkan mampu memberikan inovasi produk yang dapat mengatasi permasalahan defisiensi zink pada balita. Penelitian ini bertujuan untuk mengkaji pengaruh konsentrasi fortifikan inorganic (ZnO) terhadap sifat fisik (penampilan fisik, densitas kamba, dan daya rehidrasi) dari produk instan. Bubur bayi instan yang dihasilkan melalui tahap pembuatan tepung, fortifikasi zink, dan tahap pembuatan bubur bayi instan. Bubur bayi instan tanpa fortifikan digunakan sebagai variabel kontrol. Hasil penelitian menunjukkan bahwa konsentrasi zink pada bubur bayi instan berhasil meningkat, namun tingkat efektifitas dari fortifikasi sangat rendah. Fortifikasi inorganik zink dapat menurunkan 27,6% nilai densitas kamba dan mampu menaikkan 15% daya rehidrasi dibandingkan dengan bubur bayi instan tanpa fortifikan. Terdapat perubahan warna dari bubur bayi instan setelah mengalami proses fortifikasi zink.
ANALISA PEMANFAATAN KOMPOS SEBAGAI MEDIA BIOCOVER DI TEMPAT PEMROSESAN AKHIR SAMPAH: Studi Kasus Kota Depok, Jawa Barat Gabriel Andari Kristanto; Dwi Rahayu; Evy Novita
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (605.087 KB) | DOI: 10.14710/reaktor.15.2.117-125

Abstract

High percentage of organic waste in urban areas makes composting as good alternative in waste processing. However, composting has not been effectively used and the result is not optimal. Previous studies found compost can be used as biocover media to reduce methane emission landfill. The objective of the study is to identify the characteristic of produced at temporary waste unit Depok, West Java and the effect of compaction toward the amount of methane removal in the landfill. Before applied as biocover media, compost was characterized followed by maturation process. Study on methane removal efficiency was conducted as batches in four reactors for 35 days with compaction rate varying from 750, 800, 850 dan 900 kg/m3. Composting media used in the research had 80 cm thickness with artificial gas consisting of 50% CH4 dan 50% CO2. Initially, compost did not meet criteria as mature compost based on SNI 19-7030-2004, and as media biocover hence a pre-treatment was needed to improve the quality compost to meet the requirements. Compaction rate of 900 kg/m3has highest elimination capacity of methane i.e. 98,31%±3,6% and 13,98±4,32 g/m3/hour.
HIDROLISIS SELULOSA MENJADI GLUKOSA DENGAN KATALIS HETEROGEN ARANG AKTIF TERSULFONASI Didi Dwi Anggoro; Purwanto Purwanto; Rispiandi Rispiandi
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (667.496 KB) | DOI: 10.14710/reaktor.15.2.126-131

Abstract

CELLULOCE HYDROLYSIS TO GLUCOSE USING ACTIVE CARBON SULPHONATED HETEROGENOUS CATALYST. Enzimatic process and acid hydrolysis process are common process for conversion of cellulose to glucose. Unfornately, the two processes are expensive process and korosif process. Hence, the new process, that use sulfonaned active carbon catalyst is important to developing. The sulfonated active carbon is made from carbonated coconut sheel under temperature at 350oC. After carbonation, sulfonated active carbon soaked under sulphate acid 96% at 150oC until 15 hours. The result is then washed and dried, and tested catalyst characteristics in the form of H+ capacity, pore size catalysts by used BET surface area, functional groups by used FTIR, and morphology catalyst structure by used SEM. Catalyst performance was tested in an autoclave reactor through a hydrothermal process with difference of the catalyst amount and temperature. The results showed that the test characteristics of H+ capacity is 2.95 mmol/g, the pore size is 29 m2/gr. FTIR analyze showed that the presence of sulfonate groups read at a wavelength of vibration 1750 cm-1 and 1379 cm-1. By SEM analyze showed that the morphological structure of sulfonated active carbon is more open than other catalyst. By testing catalyst, the highest conversion of glucose is 87.2 %. Keywords: cellulose; glucose; sulfonate active carbon; thatch Abstrak Teknologi yang sudah digunakan dalam mengubah selulosa menjadi glukosa adalah dengan proses enzimatik dan hidrolisis asam. Kedua teknologi tersebut masih memiliki kendala teknis, yaitu  harga enzim yang mahal, proses yang korosif dan menimbulkan limbah, sehingga diperlukan pengembangan teknologi baru salah satu diantaranya yaitu dengan metode katalis heterogen berupa karbon aktif tersulfonasi. Karbon aktif tersulfonasi ini dibuat dari tempurung kelapa yang dikarbonisasi pada temperatur 350oC, selanjutnya direndam dalam asam sulfat 96% pada temperatur 150oC selama 15 jam. Hasilnya kemudian dicuci dan dikeringkan, dilakukan uji karakteristik dan performance (kinerja ) katalis berupa kapasitas H+, ukuran pori katalis dengan BET, uji gugus fungsi dengan FTIR, dan uji struktur marfologi katalis dengan SEM. Kinerja katalis diuji dalam reaktor autoclave melalui proses hidrotermal dengan mevariasikan jumlah katalis, dan variasi temperatur. Hasil penelitian menunjukkan untuk uji karakteristik kapasitas H+ sebesar 2,95 mmol/gr, untuk uji BET ukuran pori 29 m2/gr , untuk uji FTIR keberadaan gugus sulfonat terbaca pada vibrasi panjang gelombang 1750 cm-1 dan 1379 cm-1 , pada uji SEM struktur morfologi katalis yang lebih terbuka pada karbon aktif setelah proses sulfonasi. Kinerja katalis konversi tertinggi selulosa menjadi glukosa mencapai 87,2% pada jumlah alang-alang 2 gr, jumlah katalis 2 gr, dan temperatur 170oC selama  8 jam. Kata kunci : selulosa; glukosa; karbon aktif tersulfonasi; alang-alang
PRODUKSI BIOHIDROGEN DARI HIDROLISAT AMPAS TAHU SECARA FERMENTASI ANAEROB MENGGUNAKAN KULTUR CAMPURAN Amir Husin; Sarto Sarto; Siti Syamsiah; Imam Prasetyo
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (599.85 KB) | DOI: 10.14710/reaktor.15.2.87-96

Abstract

Ampas tahu merupakan produk samping industri pengolahan tahu berbahan dasar kacang kedelai (Glysine max.).  Dalam studi ini, ampas tahu yang telah mengalami perlakuan-awal dengan metode yang berbeda dikonversi menjadi hidrogen menggunakan kultur campuran.  Pengaruh perlakuan-awal asam satu-tahap (0,5% dan 10% berat HCl) dan dua-tahap (tahap I 0,5%  dan tahap II 10% berat HCl) terhadap sakarifikasi ampas tahu juga diinvestigasi.  Lebih lanjut, pengaruh perlakuan awal asam satu-tahap maupun dua-tahap terhadap produksi hidrogen dan efisiensi degradasi gula tereduksi dibandingkan.  Yield total gula-tereduksi 503,73 mg/g ampas tahu diperoleh dari perlakuan-awal asam dua-tahap.  Nilai ini kurang lebih 4 kali lebih tinggi dibanding hasil dari perlakuan-awal asam satu-tahap menggunakan 0,5% berat HCl. Studi produksi biohidrogen dilakukan secara batch menggunakan kultur campuran dengan kondisi reaksi  35oC dan pH awal 6,5,  Hasil percobaan menunjukkan, bahwa yield hidrogen kumulatif  maksimum 0,928  mmol/g  ampas tahu diperoleh dari perlakuan  asam dua-tahap  atau meningkat 1,8 kali dibanding perlakuan satu-tahap menggunakan 0,5% berat HCl. Key words : ampas tahu,  perlakuan asam, produksi hidrogen Abstract Tofu solid waste is one of the by-products of tofu-processing industry.  In this study, batch experiments were carried out to convert tofu solid waste pretreated by different methods into hydrogen using mixed culture.  The effects of one-stage (0.5% or 10% HCl) and two-stage (first stage 0.5% HCl) and second stage 10% HCl) pretreatments on the saccharification of tofu solid waste were also studied.  Furthermore, the effects of  and/or  two- stages acid pretreatments on hydrogen production and degradation efficiencies the reducing-sugar (RS) were compared.  A maximum total RS yield of 503.73 mg/g-tofu solid waste was obtained from substrate pretreated with two-stages method.  It was approximately 4-fold greater than that from substrate pretreated with one-stage method using 0.5% wt HCl. At the reaction condition of 35oC, initial pH =  6.5, and RS concentration based on 2 grams of tofu solid waste pretreated, a maximum cumulative hydrogen yield was 0.928  mmol/g-tofu solid waste from substrate  pretreated  with  two-stages method.  It was approximately 1.8-fold greater than that from substrate pretreated with one-stage method using 0.5% wt HCl. The results show that two-stage acid preteatment can enhancing the amount of  reducing sugar in the mixture and hydrogen yield from tofu solid wastes. 
KINETIKA REAKSI SINTHESIS BIOMATERIAL HIDROXYAPATITE DENGAN JENIS PREKURSOR NITRAT DAN ASETAT Adhi Setiawan; W Widiyastuti; Sugeng Winardi; Agung Nugroho
Reaktor Volume 15, No.2, OKTOBER 2014
Publisher : Dept. of Chemical Engineering, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (950.596 KB) | DOI: 10.14710/reaktor.15.2.104-110

Abstract

Hidroxyapatite (HAp) merupakan salah satu biomaterial yang banyak diaplikasikan dalam dunia medis untuk membuat implant jaringan tubuh terutama tulang dan gigi sehingga kemurnian produk HAp memegang peranan yang cukup penting. Agar diperoleh HAp dengan kemurnian tinggi, kinetika reaksi pembentukan HAp harus diketahui secara jelas. Metode yang digunakan untuk memperoleh kinetika reaksi HAp adalah dengan analisis TG-DTA  yang dilakukan pada dua jenis prekursor HAp yaitu asetat dan nitrat. Metode TG-DTA tersebut dilakukan dengan memanaskan prekursor HAp dengan variasi laju pemanasan 10, 15, 17, dan 20 oC/menit. Hasil analisis TG-DTA menunjukkan bahwa reaksi dekomposisi prekursor asetat dan nitrat membentuk HAp masing-masing terjadi pada suhu 659 oC dan 560 oC. Hasil fitting parameter kinetika menunjukkan bahwa energi aktivasi pembentukan HAp pada prekursor asetat sebesar 161,56 kJ/mol  dengan model kinetika Normal Grain Growth sedangkan pada prekursor nitrat sebesar 374 kJ/mol dengan model kinetika Johnson-Mehl-Avrami. Kata kunci: Biomaterial, hidroxypapatite, Dekomposisi, Energi Aktivasi ABSTRACT KINETIC STUDY OF THE BIOMATERIAS HIDOXYAPATITE SINTHESIS WITH PRECURSOR NITRATE AND  ACETATE. Hidroxyapatite (HAp) is one of the biomaterials widely applied in the medical world to make implant tissues of the body, especially bones and teeth so that the purity of the HAp plays a fairly important. In order to obtain high purity HAp, reaction kinetics should be known clearly. TG-DTA  is method used to obtain the reaction kinetics of HAp.TG-DTA analyzes were conducted on precursors acetate and nitrate. TG-DTA method is carried out by heating HAp precursor with variation heating rate 10, 15, 17, and 20° C/min respectively. The results of TG-DTA  showed decomposition precursor acetate and nitrate formed HAp occurs on temperature 659° C and 560° C respectively. The results of the fitting kinetic showed activation energy of  the HAp formation on acetate precursors about 161.56 kJ/mol with Normal Grain Growth kinetic model whereas the nitrate precursor about 374 kJ/mol with Johnson-Mehl-Avrami  kinetic model.

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