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BATCH INJECTION POTENTIOMETRY ASAM ASPARTAT, ASAM GLUTAMAT DAN ARGININ MENGGUNAKAN ELEKTRODA TUNGSTEN OKSIDA Muflihah, Yeni Maulidah; Masruroh, Heny; Zulfikar, Zulfikar
Alchemy Jurnal Penelitian Kimia Vol 10, No 1 (2014)
Publisher : Alchemy Jurnal Penelitian Kimia

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Abstract

The presence of aspartic acid, glutamic acid and arginine in solution can be detected by potentiometric method using tungsten oxide electrode in a batch system. Characterization of tungsten oxide electrode used include linear range, limit of detection, sensitivity and reproducibility. Buffer type and concentration effect also studied to optimize the measurement results. Optimum conditions for detecting arginine was at pH 6.0 with a phosphate buffer concentration of 0.5 x 10-3 M. Correlation coefficient was obtained for 0.9864, the detection limit of 5.24 x 10-6 M, sensitivity 16.1 mV/decade with reproducibility 0 –7 %. Glutamic acid has a correlation coefficient of 0.9789, the detection limit of 3.80 x 10-6 M, the sensitivity of 9.2 mV/decade and reproducibility of 0 – 6 %. Aspartic acid has a correlation coefficient of 0.9949, the detection limit of 7.76 x 10-6 M, sensitivity of 13.4 mV/decade and reproducibility of 0 – 5 %.
Analisis Ion Fe3+ dan Konduktivitas pada Air Sumur di Sekitar TPA Pakusari secara Simultan Menggunakan Metode Sequential Injection Analysis Mindarti Sartikasari; Tri Mulyono; Yeni Maulidah Muflihah
BERKALA SAINSTEK Vol 6 No 1 (2018)
Publisher : Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.19184/bst.v6i1.7762

Abstract

Analisis Fe3+ dan konduktivitas pada air sumur di sekitar TPA Pakusari perlu dilakukan untuk mengetahui kualitas perairan Penelitian ini mengembangkan metode penentuan konsentrasi Fe3+ dan konduktivitas secara simultan dan otomatis dengan menggunakan Sequential Injection Analysis (SIA). Desain SIA dibuat dengan cara menghubungkan syringe pump, selection valve dan kuvet FIA dengan menggunakan pipa kapiler PTFE, sedangkan konduktometer dihubungkan langsung dengan komputer. Salah satu parameter yang memepengaruhi metode ini yaitu volume reagen (KSCN 2M) dan laju alir analit. Hasil penelitian menunjukkan bahwa laju alir optimum pada 100 μL/s dan volume KSCN 2M optimum pada 6 μL. Metode ini diaplikasikan langsung untuk menentukan kualitas perairan di sekitar TPA Pakusari. Pengambilan sampel diambil delapan itik di sekitar TPA Pakusari diperoleh hasil bahwa titik 30 meter sebelah utara penampungan air lindi memiliki konsentrasi Fe3+ melebihi ambang batas yang telah di tetapkan KEPMENKES.RI.No. 907/MENKES/SK/VII/2002 dengan konduktivitas yang lebih tinggi dibandingkan air sumur yang lain.Kata Kunci: Fe3+, simultan, SIA, konduktivitas, air lindi
Pengaruh Variasi Waktu Penguapan Terhadap Kinerja Membran Selulosa Asetat pada Proses Ultrafiltrasi Dewi Rara Amiyati; Dwi Indarti; Yeni Maulidah Muflihah
BERKALA SAINSTEK Vol 5 No 1 (2017)
Publisher : Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.19184/bst.v5i1.5368

Abstract

Penelitian ini mempelajari pengaruh variasi waktu penguapan terhadap kinerja membran selulosa asetat. Pada proses ultrafiltrasi, selulosa asetat dibuat dengan menambahkan polietilen glikol (PEG) sebagai agen pembentuk pori membran dan meningkatkan nilai fluks membran. Pembuatan membran selulosa asetat dilakukan dengan metode inversi fasa. Variasi waktu penguapan yang digunakan selama 0, 1, 3, dan 5 menit. Membran selulosa asetat yang terbentuk dikarakterisasi meliputi uji porositas, fluks dan rejeksi. Hasil penelitian menunjukkan waktu penguapan selama 5 menit menghasilkan membran yang lebih rapat. Hasil pengukuran porositas, fluks dan rejeksi terhadap dekstran 500 kDa berturut-turut sebagai berikut: 53,35%; 4,078 (L/jam.m2) dan 92,917%. Kata Kunci: Porositas, Selulosa Asetat,Waktu Penguapan.
High Performance Liquid Chromatography of Amino Acids Using Potentiometric Detector With A Tungsten Oxide Electrode Yeni Maulidah Muflihah; Zulfikar Zulfikar; Siswoyo Siswoyo; Asnawati Asnawati; Qurrota Ayun
UNEJ e-Proceeding 2016: Proceeding The 1st International Basic Science Conference
Publisher : UPT Penerbitan Universitas Jember

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Abstract

High Performance Liquid Chromatography (HPLC) method combine with potentiometric detector was applied as a method for analysis of amino acids (aspartic acid, glutamic acid and arginine). The separation was carried out on a C18 column with isocratic elution of  a mixture of acetonitrile and phosphat buffer. Potentiometric detector using a tungsten oxide electrode as working electrode and Ag/AgCl as refference electrode. The detection method was based on the presence of H+ ions from amino acids. This application was a development of previous studies that was succesfully applied to detect the presence of amino acids in batch and flow systems. Amino acid determination was characterized by its retention time. Retention time of aspartic acid, glutamic acid and arginine were as follow: 8,46; 13,0; and 15,21 minutes. The optimized separation conditions obtained at a flow rate of 1,2 mL/min with 15% acetonitrile concentration, buffer pH 6,5 with phosphat concentration of 5x10-4 M. Detector performance tested by the recovery test of samples, and the results obtained for glutamic acid, aspartic acid and arginine respectively: 89,1%, 94,9%, and 110%. Linear range obtained at 10-3 M to 10-7 M.  Detection limit were 1,58x10-7 M for glutamic acid, 6,58x10-8 M for aspartic acid and 6,51x10-8 M for arginine.
Simultaneous Determination of Magnesium (Mg2+) and Ammonium (NH4+) by Flow Injection Analysis Mulik Kholifa; Tri Mulyono; Yeni Maulidah Muflihah
Jurnal ILMU DASAR Vol 19 No 1 (2018)
Publisher : Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (623.294 KB) | DOI: 10.19184/jid.v19i1.5483

Abstract

An automatic method for the simultaneous determination of magnesium and ammoniun by flow injection analysis is described. This analysis used two detectors, potentiometry and spectrophotometry, for the determination of magnesium and ammonium simultaneously. Potentiometric detectors are used to detect ammonium ions, whereas spectrophotometer detectors are used to detect the presence of magnesium ions. The performance of the FIA system includes linear range linearity, limit of detection, sensitivity, reproducibility and recovery test. Spectrophotometry FIA showed good performance with several criteria of linearity with regression value of 0.9918, the detection limit of 0.06 ppm, a sensitivity of 0.0115, repeatability of less than 2% and the percent recovery of 91,6%. While potentiometric FIA showed th performance with several criteria of linearity with regression value of 0.9896, the detection limit of 0.17 ppm, a sensitivity of 40.747 mV per decade of concentration, repeatability of less than 2% and the percent recovery of 89,7%. Keywords: Flow Injection Analysis, spectrophotometry, potensiometry, simultaneous
FLOW INJECTION POTENTIOMETRIC ANALYSIS OF ASPARTIC ACID, GLUTAMIC ACID AND ASCORBIC ACID USING PLATINUM ELECTRODES Yeni Maulidah Muflihah; Siswoyo Siswoyo; Tanti Haryati; Kiki Puji Setianingrum
Jurnal ILMU DASAR Vol 13 No 1 (2012)
Publisher : Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (314.474 KB) | DOI: 10.19184/jid.v13i1.886

Abstract

The presence of  weak acids in solution can be detected using a potentiometric detector. Platinum was used as a working electrode and Ag/AgCl as a reference electrode. Ascorbic, glutamic and aspartic acid were detected by a platinum electrode in a flow potentiometric system. The influence of pH, flow rate and concentration of phosphate buffers asa a carrier were studied and showed an optimum pH for the detection of ascorbic and glutamic acid at pH 6,5 and pH 7,0 for aspartic acid. Phosphate buffer concentration optimum at 1x10-4M and flow rate of 1,00 mL/min. Linear range for ascorbic and glutamic acid at 2,5 x10-4M to 5x10-2M, with a regression coefficient of  0,974 and 0,958, while for aspartic acid 5x10-4M to 5x10-2M with a regression coefficient 0,911. Detection limit for ascorbic and glutamic acids were 5x10-4M and 1x10-3M for aspartic acid. Sensor reproducibility obtained from variation coefficient  (Kv). Variation coeffiecient (Kv) of ascorbic acids 1,32-1,69%, glutamic acids 0,69- 1,57% and aspartic acid 0,54- 1,29%.
Determination of Zone Degradation for Sulfide (S2-) and Ammonia (NH3) in the Leachate from TPA Pakusari (Pakusari Landfill), Jember, Using Spectrophotometric Method Chatarina Wijayanti; Siswoyo Siswoyo; Mukh. Mintadi; Yeni Maulidah Muflihah
Indonesian Chimica Letters Vol. 1 No. 1 (2022)
Publisher : Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (674.69 KB) | DOI: 10.19184/icl.v1i1.4

Abstract

Leachate as a result from waste decomposition at landfills potentially contain toxic materials, including metals and organic matters. This leachate produces several environmental issues, including groundwater and surface water resources contamination. The landfill leachate can penetrate to the soil, blend with the soil water, flow to the soil surface, and then disembogue at the river channel. The contamination processes will vary depending on the contaminating substances and their degradation zone. Our study focused on analyzing sulfide and ammonia in the leachate. The sulfide and ammonia degradation zone have been determined by measuring the concentration of sulfide and ammonia using Spectro quant NOVA 60. The degradation zone determination ranged from the distances: 0 m, 50 m, 100 m, 150 m, and 200 m direct to the north, south, and west, and at distances of 0 m and 400 m in the east direction. The range of degradation zone based on the concentration of sulfide, ammonia, and DO (dissolved oxygen) was in a range between 150 m and 200 m from the leachate water reservoir located at TPA Pakusari (Pakusari Landfill) Jember.
The Permeation of High Concentration Hydrogen Sulfide (H2S) Gas Using PTFE (Polytetrafluoroethylene) and PVDF (Polyvinylidene Fluoride) membranes Asnawati Asnawati; Diah Ayu Nur Sholehah; Dwi Indarti; Tri Mulyono; Bambang Piluharto; Yeni Maulidah Muflihah
Indonesian Chimica Letters Vol. 1 No. 2 (2022)
Publisher : Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1165.574 KB) | DOI: 10.19184/icl.v1i2.202

Abstract

Hydrogen sulfide (H2S) is a toxic, corrosive, and flammable gas. The presence of H2S gas can be reduced by a permeation method using PTFE (Polytetrafluoroethylene) membranes and PVDF (polyvinylidene fluoride) membranes. This H2S gas passed through the membrane and was then captured by the SAOB (Sulfide Anhydride Oxidant Buffer) in S2- species form. A visible spectrophotometer was applied for the analysis of passed H2S gas. Using a PTFE membrane, the optimum flow rate was obtained at 14.71 mL/min, with a mass flux of 0.825 kg/m2.hour, permeability coefficient of 0.696 kg/m2.hour.bar, and percent removal of H2S gas was 88.14%. The optimum flow rate for the SAOB was obtained at a rate of 0.30 mL/min with a mass flux of 0.843 kg/m2.hour and a percent removal of H2S gas of 89.98%. Based on the results obtained on the PVDF membrane, the mass flux produced in the optimization of H2S gas is 0.742 kg/cm2.hour, and the optimization of the SAOB solution is 0.754 kg/cm2.hour. The resulting permeability coefficient value is 0.741 kg/cm2.hour. The results indicate that this study can remove H2S gas at the optimum H2S gas flow rate of 4.76 mL/minute of 94.89% and the optimum SAOB flow rate of 0.3 mL/minute of 95.66%