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Abstrak :
Logam berat seperti timbal (Pb) merupakan salah satu unsur jejak (trace element) yang bersifat sangat toksik bahkan pada konsentrasi yang sangat rendah. Aktivitas industri merupakan sumber utama limbah Pb di lingkungan. Maka dari itu diperlukan metode dengan limit deteksi rendah serta selektivitas tinggi untuk meningkatkan efisiensi pemisahan dan analisis Pb dari lingkungan seperti metode prakonsentrasi. Metode prakonsentrasi yang paling umum digunakan adalah Solid-Phase Extraction (SPE). Pada penelitian ini disintesis Pb(II)- ion-imprinted polymer (IIP) untuk meningkatkan selektivitas dan sensitivitas metode ekstraksi fasa padat (II) menggunakan ion Pb2+ sebagai ion template, asam galat sebagai ligan, 4-vinilpiridin sebagai monomer fungsional, AIBN sebagai inisiator, dan EGDMA sebagai agen pengikat silang. Sintesis IIP menggunakan gelombang ultrasound bertujuan untuk meningkatkan efisiensi polimerisasi. NIP sebagai pembanding disintesis dengan metode yang sama, tanpa menggunakan template. Hasil sintesis Pb(II)-IIP dan NIP dikarakterisasi menggunakan FTIR, SEM-EDS, TGA. Pb(II)-IIP 1:1 memiliki kapasitas adsorpsi paling besar yaitu 123,812 mg/g optimum pada pH 6 dan waktu kontak 120 menit. Isoterm adsorpsinya mengikuti isoterm Freundlich dan kinetika adsorpsinya mengikuti persamaan pseudo-orde dua. Parameter validasi linearitas menghasilkan nilai R2 = 0,9882, repeatabilitas dengan nilai RSD 0,086%, selektivitas terhadap logam biner Pb/Fe, Pb/Zn, Pb/Cd, Pb/Cu, dan Pb/Cr menghasilkan nilai α berurutan 16,6; 52,5; 39,2; 18,5; dan 24 yang berarti Pb(II)-IIP selektif terhadap Pb dibanding logam kompetitornya, dan uji rekoveri menunjukan hasil dengan akurasi yang baik dengan nilai persen rekoveri 104,180%; 105,431%; dan 104,262%. ......Lead (Pb) is a heavy metal that is extremely toxic even at low concentrations. Pb waste in the environment comes primarily from industrial activity. To improve the efficiency of the separation and analysis of Pb from the environment, a method with a low detection limit and good selectivity, such as the preconcentration method, is required. Solid-Phase Extraction is the most popular preconcentration technique (SPE). Using Pb2+ ions as template ions, gallic acid as ligand, 4-vinylpyridine as functional monomer, AIBN as an initiator, and EGDMA as a crosslinking agent, a Pb(II)-ion-imprinted polymer (IIP) was synthesized to improve the selectivity and sensitivity of the solid phase (II) extraction method. The goal of ultrasound-assisted IIP synthesis is to improve polymerization efficiency. NIP was synthesized using the same method as NIP, but without the use of a template. FTIR, SEM-EDS, and TGA were used to characterize the results of the Pb(II)-IIP and NIP synthesis. The adsorption capacity of Pb(II)-IIP 1:1 is the highest, with 123.812 mg/g optimal at pH 6 and a contact time of 120 minutes. The Freundlich isotherm is followed by the adsorption isotherm, and the pseudo second order equation is followed by the adsorption kinetics. The linearity validation parameter resulted in the value of R2 = 0.9882, the reliability with the RSD value 0.086%, selectivity to binary metals Pb/Fe, Pb/Zn, Pb/Cd, Pb/Cu, and Pb/Cr resulted in sequential values: 16.6; 52.5; 39.2; 18.5; and 24, which means that Pb(II)-IIP is selective for Pb compared to its competitor metals, and the recovery test shows good accuracy with the percent recovery values of 104,180%; 105,431%; and 104,262%.

Abstrak :
Gas metana merupakan salah satu komponen terbesar dalam biogas yang dapat dikonversi menjadi metanol melalui reaksi oksidasi parsial. Reaksi oksidasi parsial bio-metana sebagai sumber metana dengan menggunakan katalis heterogen ZSM-5 sintesis termodifikasi oksida logam besi. Penambahan logam diharapkan dapat menghasilkan selektivitas yang lebih tinggi terhadap konversi metana menjadi metanol. Pada penelitian ini, katalis ZSM-5 alam maupun sintetik disintesis dengan metode double template menggunakan primary template TPAOH sebagai pengarah framework MFI, serta secondary template yaitu dimethyldiallyl ammonium chloride acrylamide copolymer (PDD-AM) sebagai pengarah struktur mesopori. Katalis Fe2O3/ZSM-5 alam dan sintetik yang telah disintesis, dianalisa menggunakan XRD, SEM, BET, dan FTIR. Karakterisasi dengan XRF juga dilakukan untuk mengetahui kadar %loading oksida logam besi pada katalis ZSM-5. Uji aplikasi masing-masing katalis terhadap adsorpsi menggunakan biogas sebagai sumber metana dilakukan dalam atmospheric fixed batch reactor dengan perbandingan feed CH4(biogas):N2 0,75:2. Reaksi dilakukan pada suhu 150oC dengan waktu 120 menit dengan variasi jumlah katalis dan melakukan reaksi menggunakan katalis regenerasi. Produk hasil reaksi dari masing-masing katalis dianalisa dengan GC-FID untuk mengetahui %yield metanol yang terbentuk.

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Methane gas is one of abundant component in biogas that is common to be converted into methanol through partial oxidation reaction. Partial oxidation reaction of bio-methane uses methane as its source along with the utilization of modified iron oxide with natural and/or synthetic ZSM-5 as heterogeneous catalyst. Based on recent research showed that hierarchical ZSM-5 that was modified with iron oxide produced optimum % yield of methanol in bio-methane partial oxidation reaction (Triputrananda, 2018). Addition or loading of iron is expected to produce higher selectivity towards methane conversion into methanol. Aside of that, optimization was done with variation of pore size to determine the type of catalyst and its corresponds with optimum partial oxidation conversion output. In this research, natural and/or ZSM-5 catalyst were synthesized in double template method with TPAOH as its primary template that directed to MFI framework, PDDAM as its secondary template that directed mesoporous structure. Natural and/or synthetic Fe2O3/ZSM-5 catalyst were synthesized and further be analyzed with XRD, SEM, BET, and FTIR. Characterizations of XRF was done in order to obtain loading percentage of iron oxide into the ZSM-5 catalyst. The application were done in each variation of catalyst towards adsorption with biogas as methane source that was done in atmospheric fixed batch reactor with ratio of CH4(biogas):N2 0,75:2 feed. Reactions were done under temperature of 150oC with 120 minutes duration, alongside with amount of variation on catalyst and reaction with regenerated catalyst. Products obtained from each catalyst were analyzed with GC-FID to determine % of conversion from each products obtained.

Abstrak :
Using enzymatic sensor to determine the level of captopril is an alternative method that is being widely developed. In research , made in captopril sensor using Screen Printed Electrode (SPE), because of its advantage of being practical and simple. Cu electrodeposition on SPE is being done by potential -0,480 V vs Ag½AgCl with variation of time deposition of 5, 30 and 60 second. This research finds that the optimum deposition time is 60 second by taking into loading amount of 6,92 x 10-6 gr.cm-2. Cu/SPE is then applied to the Flow Injection Analysis (FIA) system. The optimum result of sensor appears in the FIA system with at the flow rate of 0,5 mL/minute and KOH Concentration of 1 M. Cu/SPE Sensor in FIA system has LOD of 6,530 x 10-6 M and sensitivity of 308,80 μA.mM-1.cm-2. Cu/SPE sensor has good repeatability with value linearity of 0,9113 and %RSD of 1,75%. Selectivity test on the captopril to the glucose and lactose may produce better sensor. The application of Cu/SPE sensor has value %recovery of 96,29%.

Abstrak :
Cr metal adalah logam yang berbahaya bagi lingkungan. Jika terpapar ke tubuh manusia, kromium dapat menyebabkan beberapa masalah kesehatan. Menurut Badan Perlindungan Lingkungan AS (US EPA), total kontaminan kromium dalam air adalah 0,1 mg / L. Oleh karena itu, logam kromium harus dipisahkan sebelum terpapar ke tubuh manusia. Metode yang biasa digunakan untuk memisahkan logam Cr (III) dalam air adalah tidak selektif seperti adsorpsi dan elektrokimia. Ion Imprinted Polymer adalah teknik untuk menciptakan selektivitas melalui ikatan rongga pada permukaan adsorben. Selektivitas adsorben polimer didasarkan pada geometri koordinasi, jumlah koordinasi ion, muatan dan ukuran polimer. Dalam penelitian ini, sintesis Ion Imprinted Polymer dilakukan dengan template ion krom (Cr3 +) dengan asam galat sebagai ligan dan metil metakrilat sebagai monomer fungsional. Polimer imprinted Cr-ion (Cr-IIP) berhasil disintesis dengan metode polimerisasi massal menggunakan Ethylenglycoldimetaacrylate (EGDMA) sebagai pengikat silang dan Azobisisobutironitril (AIBN) sebagai Pemrakarsa. Variasi perbandingan Asam Galat: Methyl Methacrylate dipelajari dan rasio mol optimum Asam Gallic: Methyl methacrylate dipelajari yaitu 1: 1. Hasil sintesis Cr-IIP dikarakterisasi menggunakan Scanning Electron Microscope Energy Dispersive X-ray Spectroscopy (SEM) -EDX) dan Fourier Transform Infra Red (FTIR). Untuk mengetahui kemampuan adsorpsi, Cr-IIP diuji untuk pengaruh pH dan waktu kontak. Adsorpsi maksimum Cr-IIP dicapai pada pH 5 dan waktu kontak 120 menit. Adsorpsi polimer imprint-Cr-ion mengikuti model isoterm freundlich dengan kapasitas adsorpsi maksimum 131,37 mg / g. Uji selektivitas polimer imprinted Cr-ion untuk ion logam lain menunjukkan nilai relatif faktor selektivitas (αr) dari Cr (III) / Ag (I) dan Cr (III) / Fe (III) adalah 3.08 dan 3.93. Penggunaan Cr-IIP memiliki reproduksibilitas yang baik dengan CV Horwitz 1,28% dan% RSD 1,02%. Cr (III) -IIP juga menunjukkan nilai pemulihan 110,26%; 121,37% dan 110,87%.

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Cr metal is a metal which is dangerous for the environment. If exposed to the human body, chromium can cause several health problems. According to The US Environmental Protection Agency (US EPA), total chromium contaminants in water are 0.1 mg / L. Therefore, chromium metal must be separated before exposure to the human body. The commonly used method of separating Cr (III) metals in water is non-selective such as adsorption and electrochemistry. Ion Imprinted Polymer is a technique for creating selectivity through binding cavities on the surface of the adsorbent. The polymer adsorbent selectivity is based on the coordination geometry, the ion coordination number, the charge and the size of the polymer. In this research, synthesis of Ion Imprinted Polymer was carried out with a chromium ion (Cr3 +) template with gallic acid as a ligand and methyl methacrylate as a functional monomer. Cr-ion imprinted polymer (Cr-IIP) was successfully synthesized by the bulk polymerization method using Ethylenglycoldimetaacrylate (EGDMA) as a crosslinker and Azobisisobutironitril (AIBN) as an Initiator. Variation of Gallic Acid comparison: Methyl Methacrylate was studied and the optimum mole ratio of Gallic Acid: Methyl methacrylate was studied which was 1: 1. The results of Cr-IIP synthesis were characterized using Scanning Electron Microscope Energy Dispersive X-ray Spectroscopy (SEM-EDX) and Fourier Transform Infra Red (FTIR). To find out the adsorption capability, Cr-IIP was tested for the influence of pH and contact time. Maximum adsorption of Cr-IIP is achieved at pH 5 and contact time 120 minutes. The adsorption of Cr-ion imprinted polymer follows the freundlich isotherm model with a maximum adsorption capacity of 131.37 mg / g. The Cr-ion imprinted polymer selectivity test for other metal ions shows the relative value of the selectivity factor (αr) of Cr (III) / Ag (I) and Cr (III) / Fe (III) is 3.08 and 3.93. The use of Cr-IIP has good reproducibility with a CV Horwitz of 1.28% and% RSD of 1.02%. Cr (III) -IIP also showed a recovery value of 110.26%; 121.37% and 110.87%.

Abstrak :
Penentuan kadar glukosa menggunakan sensor non-enzimatik pada saat ini banyak dikembangkan sebagai alternatif, sensor glukosa non-enzimatik berupa perangkat yang praktis dan sederhana, digunakan Screen Printed Electrode (SPE) sebagai sensor, kemudian dimodifikasi dengan carbon nanotube (CNT). Pada penelitian ini, digunakan oksida tembaga sebagai sensor non-enzimatik yang terdeposit dipermukaan SPE yang telah diteteskan CNT terfungsionalisasi-OH, dengan metode elektrodeposisi menggunakan larutan CuSO4 0.01M dalam 0,1M H2SO4. Variasi banyak jumlah tetesan CNT terfungsionalisasi-OH, potensial dan waktu deposisi dilakukan untuk mendapatkan deposit Cu/CNT-SPE yang optimum, karakterisasi dengan SEM-EDS. Uji deteksi glukosa dilakukan pada potensial +0.7 V vs Ag/AgCl. Deposit Cu/CNT-SPE dengan 1 tetesan CNT terfungsionalisasi-OH pada potensial -0.65 V selama 300 detik merupakan yang paling optimum, karena mempunyai sensitifitas paling tertinggi sebesar 2514.27 µA mM-1 cm-2, batas deteksi terendah sebesar 0.842 x 10-3 M dan linieritas paling baik sebesar R2 = 0.985. Sensor deposit Cu/CNT-SPE optimum digunakan pada sistem FIA, didapatkan laju alir optimum 0,5 mL/menit, konsentrasi NaOH 1 M sebagai larutan pembawa dilihat dari %RSD sebesar 1.12% rata-rata respon arus 0.000247 A. Pada variasi konsentrasi glukosa dihasilkan linieritas sebesar R2 = 0.982 dengan sensitifitas sebesar 4261.590 µA mM-1 cm-2, batas deteksi terndah sebesar 5.769 x 10-4 M sensor memiliki repeatabilitas yang baik dengan % RSD sebesar 1.52% (n=10). Uji stabilitas selama 5 hari pengamatan dengan %RSD sebesar 1.79%. Deteksi glukosa pada minuman kemasan merk N dengan %KR 13.6%, serta mencari %recovery sampel minunan kemasan merk N didapat 98,36%. Uji interferensi pada glukosa terhadap sukrosa, fruktosa, asam askorbat, asam nitrat dan natrium karbonat. ......Determination of glucose sensor using non-enzymatic sensor has been developed as an alternative to non-enzymatic glucose sensor with practical and simple device, using Screen Printed Electrode (SPE) as sensor, which then modified with carbon nanotube (CNT). In this study, copper oxide are used as non-enzymatic sensor deposited on the surface of SPE dripped with functionalized CNT-OH, using electodeposition method with solution of 0.01 M CuSO4 in 0.1 M H2SO4. Droplets of functionalized CNT-OH, deposition potential and time are varied to find the optimal Cu/CNT-SPE deposit, characterize with SEM-EDS. Glucose detection were tested at the potential of +0.7 V vs Ag/AgCl. The test found that the optimal deposit was Cu/CNT-SPE with 1 droplet of functionalized CNT-OH at potential -0.65 V for 300 seconds, with highest sensitivity of 2514.27 µA mM-1 cm-2, lowest detection limit of 0.842 x 10-3M, and best linearity of R2 = 0.985. The optimal sensor depositition Cu/CNT-SPE electrode were used on flow system FIA, with result of optimal flow rate of 0.5 mL/min, concentration of 1 M NaOH as a carrier seen from %RSD of 1.12% with average current response 0.000247 A. The result of variation of glucose concentration was linearity of R2 = 0.981 with sensitivity 4261.590 µA mM-1 cm-2, lowest detection limit of 5.769 x 10-4M, sensor have good repeatability at %RSD of 1.52% (n=10). Stability test for 5 days resulted in %RSD of 1.79%. Glucose detection in a beverage N yielded %KR of 13.6%, and %recovery of beverage N yielded 98.36%. Interference test on glucose to sucrose, fructose, ascorbic acid, nitric acid and sodium carbonate.

Abstrak :
Pada penelitian ini dilakukan sensor glukosa non-enzimatik menggunakan deposit tembaga pada permukaan emas (Cu/Au). Deposit Cu/Au dapat disintesis dengan metode amperometri pada potensial -0,45 V vs Ag/AgCl menggunakan larutan CuSO4. Konsentrasi CuSO4 dan waktu deposisi divariasikan untuk memperoleh kondisi optimum. Kondisi optimum untuk deposisi adalah tiga menit dengan konsentrasi CuSO4 0,1 M. Hasil karakterisasi SEM dan EDS menunjukan deposit memiliki ukuran 400 - 480 nm dengan persen berat Cu sebesar 71,50%. Deposit Cu/Au dapat mendeteksi glukosa hingga konsentrasi 0,0462 mM. Deposit Cu/Au kemudian digunakan untuk mengukur kadar glukosa dalam sampel darah. Hasil pengukuran menunjukkan kadar glukosa dalam sampel darah sebesar 6,6504 mM. Nilai tersebut berbeda sebesar 9,8238% jika dibandingkan dengan pengukuran menggunakan glukosa meter yang menghasilkan nilai 6,0555 mM. ......Non-enzymatic glucose sensor using copper deposits on gold (Cu/Au) was studied in this research. Cu/Au deposits was synthesized using amperometry method at -0,45 V vs Ag/AgCl using CuSO4. The concentration of CuSO4 and deposition time were varied to obtained the optimum condition. Optimum condition of deposition was at 3 minutes and CuSO4 concentration of 0,1 M. SEM and EDS characterization showed that the size of deposits was 480 nm with percent weight 71,50% via EDS characterization. Cu/Au deposits was able to measure glucose up to 0.0462 mM. Cu/Au deposits was utilized to measure the level of glucose in blood samples. The level of glucose in blood samples was measured to be 6,6504 mM. This result differs about 9,8238% to the results obtained from glucose meter that resulted value 6.0555 mM.

Abstrak :
Overdosis parasetamol menyebabkan kerusakan pada hati dan ginjal. Analisis kandungan parasetamol sederhana, cepat, dan berbiaya rendah dengan akurasi sesuai diperlukan. Modifikasi elektroda glassy carbon (GCE) sebagai sensor elektrokimia parasetamol dengan molecular imprinted polymer (MIP) berbasis anilin dan/atau fenol dilakukan dengan elektropolimerisasi. Elektropolimerisasi MIP dibandingkan dengan elektropolimerisasi anilin dan/atau fenol dengan atau tanpa molekul cetakan. Elektroda termodifikasi digunakan untuk membuat kurva kalibrasi parasetamol (50 s.d. 1000 ppm) dengan sensitivitas oleh GCE-MIP anilin 0,022 (R2=0,997); GCE-MIP fenol 0,001 (R2=0,950); GCE-MIP anilin dan fenol 0,006 (R2=0,991). Aplikasi pengukuran pada obat pasaran mengandung parasetamol dan kafein menunjukan bahwa parasetamol terkandung dalam satu kaplet obat sebesar 513 mg dengan kesalahan sebesar 2,6% relatif terhadap nilai yang dicantumkan kemasan obat. ...... Paracetamol overdose could lead to heart and kidney damage. Simple, fast, low- cost with suitable accuracy analytical sensor of paracetamol is needed. Modification of glassy carbon electrode with molecular imprinted polymer (MIP) based on aniline and/or phenol has been succesfully done through electropolymerization. It is then compared with electropolymerization of each monomers, aniline and/or phenol, with or without the molecular template. Modified electrodes are used to make standard curves of paracetamol 50 to 1000 ppm with sensitivity by GCE-MIP aniline: 0,022 (R2=0,997); GCE-MIP phenol: 0,001 (R2=0,950); GCE-MIP aniline and phenol: 0,006 (R2=0,991). Application for measuring a drug containing paracetamol and caffeine results that there is 513 mg paracetamol in a tablet with 2.6% error relative to the value listed in drug's packaging.

Abstrak :
Pencemaran limbah cair industri zat warna di Indonesia telah menjadi permasalahan lingkungan yang serius. Beberapa metode yang digunakan untuk mengatasi limbah zat warna diantaranya filtrasi membran, ozonisasi, klorinasi, proses elektrokimia, fotodegradasi, koagulasi flokulasi, oksidasi kimia, oksidasi biologi, dan adsorpsi. Adsorpsi memilki kelebihan yaitu berbagai macam bahan adsorben, preparasi dan operasi mudah, nilai ekonomis tinggi, efisiensi tinggi, reusabilitas baik, cocok untuk beragam zat warna ramah lingkungan dan dapat digunakan untuk menghilangkan pewarna organik dalam perairan dengan skala besar. Beragam adsorben dengan struktur pori dan luas permukaan spesifik telah dipelajari, salah satunya MOFs. MOFs memiliki keunggulan seperti luas permukaan spesifik yang tinggi, porositas yang baik, dan ukuran pori terkontrol. Dalam penelitian ini MOFs jenis MIL-101 (Fe) disintesis menggunakan logam Fe yang ramah lingkungan dan ligan BDC dengan metode solvothermal. Variasi suhu 100oC dan 120oC, jumlah prekursor FeCl3.6H2O 2,45 mmol, 4,9 mmol, dan 9,81 mmol dan jenis pelarut yaitu DMF dan campuran pelarut DMF : Aquades dengan perbandingan 2 : 3 dipelajari pengaruhnya terhadap sintesis MOF, MOF hasil sintesis kemudian diaplikasikan sebagai adsorben zat warna Methylene Blue dan Rhodamine B dalam air. Hasil sintesis dikarakterisasi menggunakan FTIR, XRD, TGA, BET, dan SEM untuk mengetahui ikatan kimia, topologi kerangka, kristanilitas, luas permukaan, dan stabilitas termal. Hasil karakterisasi menunjukan variasi suhu dan prekusor dihasilkan MOF dengan struktur polimorfik MIL-88B. Aplikasi adsorpsi zat warna Methylene Blue dan Rhodamine mencapai kapasitas absorpsi optimum pada pH 9 dan waktu kontak 180 menit adsorpsi Fe-BDC MOF pada Methylene Blue dan Rhodamine B mengikuti pemodelam isoterm adsorpsi Langmuir dengan kapasitas adsorpsi maksimum berturut-turut sebesar 162,82 mg/g dan144,65 mg/g. Kata Kunci: Fe-Metal Organic Frameworks, Methylene Blue, Rhodamine B, Adsorpsi, Ligan BDC (Asam 1,4-benzena dikarboksilat), metode solvothermal.

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The industrial dye-wastewater has been a tremendous environmental problem in Indonesia. Several techniques have been used to eliminate dye-waste water, such as membrane filtration, chlorinaton, ozonation, coagulation-floculation, chemical oxidation, biology oxidation, and adsorption. Adsorption technique is extensively used for removal of the dye-wastewater due the excellent properties of its method, having various of adsorbent material, simple preparation and operation, low cost, high efficiency, good reusability and capable of reducing the organic dyes widely. In this case, many adsorbents, having tunable pore and specific surface area, have been studied. MOFs have some advantages as adsorbents in that their large surface area, tunable pore size, and adjustable porosity. In this work, MOFs type MIL-101 (Fe) was synthesized assisted solvothermal reactions at 100 oC and 120 oC, and various amount of FeCl3.6H2O precursor of 2.45 mmol, 4.9 mmol, and 9.81 mmol. The effect of solvents in the synthesis was studied by using DMF and mixture of DMF: distilled water 3 : 2. Briefly, MIL-101 was synthesized with environmental friendly metal precursor, FeCl3.6H2O, and 1,4 benzenedicarboxylate (BDC) ligands. The material characteristics of the as-synthesized Fe-BDC MOF such as structure and topology of MOFs, surface area, and thermal stability were studied using XRD, FTIR, BET, TGA, and SEM. The XRD patterns show that the crystals of MIL101 was successfully formed with some impurities of MIL-88B. The application of Fe-BDC MOF as adsorbent for Methylene Blue (MB) and Rhodamine B (RhB) in aqueous solution is learned. The optimum adsorption condition showed when 5 mg Fe-BDC MOF is applied to the dyes after 180 minutes at pH 9. It was found that the isotherm data for Methylene Blue and Rhodamine B had a good correlation with the Langmuir isotherm. The maximum adsorption capacity of MOF was able to reach 162,82 mg/g for Methylene Blue and 144,65 mg/g for Rhodamine B. Keyword(s): Fe-Metal Organic Frameworks, Methylene Blue, Rhodamine B, adsorption, 1,4 benzenedicarboxylate (BDC), and solvothermal method.

Abstrak :
Penentuan kadar glukosa secara elektrokimia menggunakan oksida logam sebagai pengganti enzim mulai dikembangkan beberapa tahun terakhir. Pada penelitian ini, oksida tembaga digunakan sebagai sensor glukosa non-enzimatik dengan mengoksidasi glukosa menjadi glukonolakton. Oksida tembaga diperoleh dengan elektrodeposisi larutan CuSO4 0,1 M dalam H2SO4 0,1 M pada elektroda kerja karbon pasta dengan variasi waktu dan potensial deposisi untuk menperoleh kondisi deposit Cu yang optimum. Untuk mendeteksi glukosa, deposit Cu digunakan sebagai elektroda kerja dengan metode siklik voltametri dalam larutan NaOH 1 M. Deposit Cu yang dielektrodeposisi pada potensial -0,366 V selama 120 detik merupakan kondisi optimum untuk pendeteksian glukosa karena mempunyai sensitivitas yang tertinggi sebesar 1183,5996 μA mM-1 cm-2, batas deteksi paling rendah sebesar 0,6728 mM, dan nilai linearitas paling baik r2 = 0,9988 pada rentang konsentrasi 1,664 ? 62,5 mM. Sensor ini mempunyai repeatabilitas yang baik dengan %RSD = 1,32 % (n=10), stabil dalam waktu pengujian selama 5 hari dengan %RSD = 1,51 % (n=5), dan sangat selektif terhadap glukosa dari zat pengganggu seperti asam askorbat, asam urat, sukrosa dan fruktosa. Sensor dengan oksida tembaga ini dibandingkan dengan sensor non-enzimatik pada pengujian kadar glukosa dalam darah dan menunjukkan perbedaan hasil sebesar 21,45 %. ......The electrochemical determination of glucose concentration using metal oxide as a substitute of enzyme is being developed in recent years. In this research, copper oxide is used as a non-enzymatic glucose sensor by oxidating glucose to gluconolactone. Copper oxide was obtained by electrodeposition using CuSO4 0,1 M in H2SO4 0,1 M solution at carbon paste electrode with the variation of potensial and time of deposition to show the optimum condition of copper deposit. For detecting glucose, Copper deposit was used as working electrode by voltammetry cyclic method in NaOH 1 M solution. Copper deposit which was deposited in -0,366 V potential for two minutes was the optimum condition because of the highest sensitivity 1183,5996 μA mM-1 cm-2 , the lowest limit of detection 0,6728 mM, and the best linearity r2 = 0,9988 in concentration range 1,664 -62,5 mM. This sensor exhibited a good repeatability with %RSD = 1,32 % (n=10), showed high stability in five consecutive days of detection with %RSD = 1,51 % (n=5), and had a good selectivity of glucose in the presence of interfering spesies such as ascorbic acid, uric acid, fructose, and sucrose. This copper oxide-based glucose sensor was compared by enzymatic glucose sensor in blood-sugar detection and exhibited % relative error = 21,45 %.

Abstrak :
Kecenderungan terhadap penyakit diabetes mellitus membuat teknologi untuk mengukur konsentrasi glukosa dikembangkan, salah satunya dengan membuat sensor glukosa non-enzimatik. Pada penelitian ini, dikembangkan sensor glukosa non-enzimatik berbasis oksida Ni. Ni dideposisi pada elektroda karbon pasta (Ni/CPE) dengan potensial deposisi dan waktu deposisi divariasikan. Hasil deposisi dikarakterisasi dengan SEM-EDS. Kemudian deposit Ni diaktivasi dalam NaOH 1 M menjadi NiO(OH) yang dapat mengoksidasi glukosa menjadi glukonolakton sehingga dapat dideteksi secara elektrokimia. Hasil penelitian menunjukkan bahwa Ni/CPE dapat digunakan untuk mendeteksi glukosa pada rentang konsentrasi 1,66 mM - 62,50 mM dengan linearitas R2=0,999 pada potensial deposisi -0,972 V vs Ag|AgCl dan waktu deposisi 3 menit. Selain itu, Ni/CPE (-0,972 V; 3 menit) memiliki kedapatulangan yang baik dengan % RSD 1,90% (n=10) dan menunjukkan stabilitas yang baik dalam kurun waktu 7 hari dengan % RSD 1,51% (n=6). Ni/CPE (-0,972 V; 3 menit) memiliki sensitivitas 527,57 μ𝐴 mM-1 cm-2 dan batas deteksi 0,45 mM. Ni/CPE (-0,972 V; 3 menit) tidak terganggu oleh kehadiran asam askorbat dan asam urat serta dapat digunakan untuk menentukan konsentrasi glukosa dalam darah pasien non diabetes dengan hasil pengukuran 5,23 mM. Nilai tersebut berbeda sebesar 14,85% jika dibandingkan dengan pengukuran menggunakan glukosameter yang menghasilkan nilai 4,55 mM. ......High tendency of diabetes mellitus caused the development of non-enzymatic glucose sensor. In this research, non-enzymatic glucose sensor is proposed based on Ni/CPE. Ni/CPE was prepared by electrodeposition of Ni on the carbon paste electrode (CPE) with various deposition potential and deposition time. Ni deposit was characterized by SEM-EDS. After that, Ni deposit was oxidized to NiO(OH) in alkaline solution (NaOH 1 M). NiO(OH) had a role as catalyst of glucose oxidation to gluconolactone. Ni/CPE was used to detect glucose with linear range from 1,66 mM - 62,50 mM (R2=0,999). The best linearity result of deposition potensial and deposition time was achieved at -0,972 V vs Ag|AgCl and 3 minutes. Furthermore, Ni/CPE (-0,972 V; 3 minutes) showed a good repeatability with % RSD 1,90% (n=10) and good stability for 7 days with % RSD 1,51% (n=6). Ni/CPE (-0,972 V; 3 minutes) resulted sensitivity 527,57 μ𝐴 mM-1 cm-2 and LOD 0,45 mM. Oxidable species such as ascorbic acid and uric acid show no significant interference in determination of glucose. Ni/CPE (-0,972 V; 3 minutes) was used to determine glucose concentration in human blood sample. The concentration of glucose in non diabetes human blood sample was measured to be 5,23 mM. This result differs about 14,85% to the result obtained from glucose meter which resulted value 4,55 mM.