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Determination of Benzoic Acid, Sodium Saccharin, And Caffeine By High Performance Liquid Chromatography Arief Yandra Putra; Fitri Mairizki; Hamzar Suryani; Safni Safni
Jurnal Litbang Industri Vol 2, No 2 (2012)
Publisher : Institution for Industrial Research and Standardization of Industry - Padang

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (98.21 KB) | DOI: 10.24960/jli.v2i2.603.79-86

Abstract

Concentrations of benzoic acid, sodium saccharin and caffeine in soft drink samples were determined by using Reverse Phase High Performance Liquid Chromatography (HPLC). The optimum analytical conditions of those three samples was methanol-phosphate buffer (1:7) as mobile phases, with pH 4.5 and flow rate 1.0 mL/min, column C18 (150x4.6 mm i.d.) as stationary phases at 400C with UV-Vis Spectrophotometer detection at 220 nm. The concentration level of those compounds observed was not beyond the maximum limit of SNI 01-011101995 for sodium saccharin and benzoic acid and SNI 01-6684-2002 for caffeine. The relative standard deviation based on retention time and peak area, as 0.37% and 0.59% for benzoic acid, 0.16% and 0.21% for sodium saccharin, 0.38% and 0.6% for caffeine. Finally, the recovery for benzoic acid, sodium saccharin and caffeine was 100.82%, 94.92% and 90.32%, respectively. The relative standard deviation and recovery of all samples met AOAC method requirements.ABSTRAKPenelitian tentang penentuan asam benzoat, natrium sakarin dan kafein telah dilakukansecara Kromatografi Cair Kinerja Tinggi (KCKT) Fasa Balik. Kondisi optimum analisis dariketiga senyawa di atas adalah fasa gerak metanol-bufer fosfat (1:7) dengan pH 4,5, laju alir 1 mL/min, kolom C18 (150 x 4,6 mm i.d.) dengan temperatur 40oC dan pendeteksiandengan Spektrofotometer UV/Vis pada panjang gelombang 220 nm. Metoda ini diaplikasikan pada beberapa sampel minuman ringan. Kadar ketiga senyawa ini di dalam sampel tidak melebihi batas maksimum yang diizinkan yaitu berdasarkan SNI 01-0222-1995 untuk natrium sakarin dan asam benzoat serta SNI 01-6684-2002 untuk kafein. Standar Deviasi Relatif ketiga senyawa ini berdasarkan waktu retensi dan luas puncak secara berturut-turut adalah; asam benzoat 0,37% dan 0,59%, natrium sakarin 0,16% dan 0,21%, kafein 0,38% dan 0,60%. Hasil perolehan kembali dari ketiga senyawa ini adalah asam benzoat 100,82%, natrium sakarin 94,92%, kafein 90,32%. Standar Deviasi Relatif dan perolehan kembali ketiga senyawa ini memenuhi persyaratan metoda AOAC.
Determination of Benzoic Acid, Sodium Saccharin, And Caffeine By High Performance Liquid Chromatography Arief Yandra Putra; Fitri Mairizki; Hamzar Suryani; Safni Safni
Jurnal Litbang Industri Vol 2, No 2 (2012)
Publisher : Institution for Industrial Research and Standardization of Industry - Padang

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (98.21 KB) | DOI: 10.24960/jli.v2i2.603.79-86

Abstract

Concentrations of benzoic acid, sodium saccharin and caffeine in soft drink samples were determined by using Reverse Phase High Performance Liquid Chromatography (HPLC). The optimum analytical conditions of those three samples was methanol-phosphate buffer (1:7) as mobile phases, with pH 4.5 and flow rate 1.0 mL/min, column C18 (150x4.6 mm i.d.) as stationary phases at 400C with UV-Vis Spectrophotometer detection at 220 nm. The concentration level of those compounds observed was not beyond the maximum limit of SNI 01-011101995 for sodium saccharin and benzoic acid and SNI 01-6684-2002 for caffeine. The relative standard deviation based on retention time and peak area, as 0.37% and 0.59% for benzoic acid, 0.16% and 0.21% for sodium saccharin, 0.38% and 0.6% for caffeine. Finally, the recovery for benzoic acid, sodium saccharin and caffeine was 100.82%, 94.92% and 90.32%, respectively. The relative standard deviation and recovery of all samples met AOAC method requirements.ABSTRAKPenelitian tentang penentuan asam benzoat, natrium sakarin dan kafein telah dilakukansecara Kromatografi Cair Kinerja Tinggi (KCKT) Fasa Balik. Kondisi optimum analisis dariketiga senyawa di atas adalah fasa gerak metanol-bufer fosfat (1:7) dengan pH 4,5, laju alir 1 mL/min, kolom C18 (150 x 4,6 mm i.d.) dengan temperatur 40oC dan pendeteksiandengan Spektrofotometer UV/Vis pada panjang gelombang 220 nm. Metoda ini diaplikasikan pada beberapa sampel minuman ringan. Kadar ketiga senyawa ini di dalam sampel tidak melebihi batas maksimum yang diizinkan yaitu berdasarkan SNI 01-0222-1995 untuk natrium sakarin dan asam benzoat serta SNI 01-6684-2002 untuk kafein. Standar Deviasi Relatif ketiga senyawa ini berdasarkan waktu retensi dan luas puncak secara berturut-turut adalah; asam benzoat 0,37% dan 0,59%, natrium sakarin 0,16% dan 0,21%, kafein 0,38% dan 0,60%. Hasil perolehan kembali dari ketiga senyawa ini adalah asam benzoat 100,82%, natrium sakarin 94,92%, kafein 90,32%. Standar Deviasi Relatif dan perolehan kembali ketiga senyawa ini memenuhi persyaratan metoda AOAC.
Studi Geologi Terhadap Analisis Kestabilan Lereng Menggunakan Metode RMR (Rock Mass Rating) Pada Jalan Daerah Koto Lamo, Kecamatan Kapur Sembilan, Sumatera Barat Husnul Kausarian; Muhammad Yusuf; Adi Suryadi; Pakhrur Razi; Fitri Mairizki
JURNAL INTEGRASI Vol 15 No 1 (2023): Jurnal Integrasi - April 2023
Publisher : Pusat Penelitian dan Pengabdian Masyarakat Politeknik Negeri Batam

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30871/ji.v15i1.5450

Abstract

geographically, the research area is located at coordinates 0°21'12."- 0° 22' 50." latitude and 00°10'53" - 100°33'44.4620" longitude. the study is in the koto lamo and surrounding areas, Kapur Sembilan district, West Sumatra Province. the purpose of this study was to determine the level of slope stability in the study area using the UCS (Uniaxial Compressive Strength) analysis method for intact rock strength, RMR (Rock Mass Rating) and stereographic. From the field data, there are 10 scanlines of the main research objects. Geological mapping shows the slopes are sandstone. From the rock analysis UCS (Uniaxial Compressive Strength), the strength of intact rock the average value of the Schmidt hammer test is 13.08, while the density value of rock samples is 25.86 KN⁄m³. From these results obtained a Uniaxial Compressive Strength (UCS) value of 19 mpa, included in the weight 2 with a weak category. Then the results of the RMR (Rock Mass Rating) analysis are worth 35.4 with RMR class IV (poor).
Co-Authors Adi Suryadi Arief Yandra Putra Hamzar Suryani Husnul Kausarian MUHAMMAD YUSUF Pakhrur Razi Safni Safni