scholarly journals SINTESIS PALMITOIL DAN LAUROIL ETANOLAMIDA MENGGUNAKAN PELARUT CAMPURAN : PENGARUH TEMPERATUR DAN WAKTU REAKSI

2018 ◽  
Vol 6 (4) ◽  
pp. 29-33 ◽  
Author(s):  
Muhammad Ashari ◽  
Nur Annisa ◽  
Zuhrina Masyithah
Keyword(s):  
Reaction Time ◽  
Mixed Solvent ◽  
Catalyst Concentration ◽  
Effect Of Temperature ◽  
Solvent Ratio ◽  
Hydrophilic Group ◽  
Amidation Reaction ◽  
Ir Spectrophotometry ◽  
Ft Ir ◽  
Substrate Ratio

Surfactant is a molecule which has hydrophilic group and a lipophilic group which can unify a mixture consisting of water and oil. Alkanolamide is a type of widely used nonionic surfactant for various purposes. In this study, we observed the effect of temperature and reaction time on the synthesis of palmitoyl ethanolamide surfactant from palmitic acid and lauroyl ethanolamide from lauric acid with zirconium (IV) chloride as catalyst in mixed solvent. This research was conducted using amidation reaction at temperature variation of 55oC, 65oC, 75oC, 85oC and 95oC, reaction time variation of 1 hour, 2 hours, 3 hours, 4 hours, and 5 hours, mole substrate ratio at 1:10, solvent ratio at 2: 1 (v / b), catalyst concentration 5% (w/w), and stirring rate at 250 rpm. Then the product was analyzed by FT-IR spectrophotometry. Based on this research, the optimum condition to synthesis palmitoyl ethanolamide surfactant was obtained at 55 oC and temperature 65 oC to synthesis lauroyl ethanolamide surfactant at reaction time of 3 hours for both of them.

scholarly journals PENGARUH JENIS PELARUT DAN TEMPERATUR REAKSI PADA SINTESIS SURFAKTAN DARI ASAM OLEAT DAN n-METIL GLUKAMINA DENGAN KATALIS KIMIA

2015 ◽  
Vol 4 (1) ◽  
pp. 25-29 ◽  
Author(s):  
Jojor Rohana Oppusunggu ◽  
Vinta Rutliana Siregar ◽  
Zuhrina Masyithah
Keyword(s):  
Surface Tension ◽  
Reaction Time ◽  
Reaction Temperature ◽  
Solvent Ratio ◽  
Hydrophilic Group ◽  
Hydrophilic Lipophilic Balance ◽  
Amidation Reaction ◽  
Ir Spectrophotometry ◽  
Ft Ir ◽  
Substrate Ratio

Surfactants are molecules that also has a hydrophilic group and a lipophilic group that can unify a mixture consisting of water and oil. Alkanolamide is one type of nonionic surfactants are widely used in everyday life. In this study, will be observed the influence of the type of solvent and reaction temperature on the synthesis of surfactant alkanolamide n -methyl glukamine and oleic acid from palm oil with sodium methoxide catalyst. This study aims to determine the value of the hydrophilic lipophilic balance (HLB), pH and surface tension of surfactant, by observing the effect of the type of solvent and reaction temperature. This research was conducted by using a flask at 90 ° C, 110 ° C, 130 ° C for 3 hours reaction time, substrate ratio of 1: 2, the stirring speed of 150 rpm and a catalyst concentration of 0.4% (w/w). In the amidation reaction samples taken from the flask every 1 hour for 3 hours and then the results of this amidation reaction was washed with acetone solvent to separate the catalyst. Results washing then purified by heating at 90°C to evaporate the solvent surfactant products hexane and butanol. Results containing surfactant in the analysis with Hydrophilic Liphophilic Balance Method, surface tension and FT-IR spectrophotometry. Based on this research, the optimal conditions at a temperature of 110oC, reaction time 3 hours at the solvent ratio 2: 1. From the analysis of surfactant oleoil n-Methyl glukamine values obtained HLB in the range of 11,53 HLB in accordance with the standard detergent.

scholarly journals SINTESIS STEARAMIDA DARI ASAM STEARAT DAN UREA MENGGUNAKAN PELARUT CAMPURAN : PENGARUH TEMPERATUR DAN WAKTU REAKSI

2018 ◽  
Vol 7 (1) ◽  
pp. 5-8 ◽  
Author(s):  
Muhammad Syukri ◽  
Zuhrina Masyithah
Keyword(s):  
Reaction Time ◽  
Optimum Condition ◽  
Stearic Acid ◽  
Mixed Solvent ◽  
Effect Of Temperature ◽  
Molar Ratio ◽  
Solvent Ratio ◽  
Hydrophilic Group ◽  
Substrate Molar Ratio

Surfactant is a molecule which has hydrophilic group and a lipophilic group which can unify a mixture consisting of water and oil. Stearamide is one kind of surfactant non-ionic which has used on any aplication. This study aims to know about optimum of temperature and time on synthesis of stearamide from stearic acid and urea with zirconium (IV) chloride in mixed solvent. This study will be observed the effect of temperature and reaction time on the synthesis of stearamide surfactant from stearic acid and urea with zirconium (IV) chloride as catalyst in mixed solvent. This research was conducted at temperature of 45°C, 55°C, 65°C, 75°C, 85°C and 95°C, reaction time of 1 hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 7 hr and 8 hr, substrate molar ratio at 1:6 (w/w), solvent ratio at 2:1 (v/v), weight of catalyst 3% (%w), and stirring speed at 250 rpm. Based on this research, the optimum condition to synthesis stearamide surfactant was obtained at 85 oC and reaction time at 3 hours.

scholarly journals PENGARUH SUHU DAN KECEPATAN PENGADUKAN PADA PROSES PEMBUATAN SURFAKTAN NATRIUM LIGNOSULFONAT DARI TEMPURUNG KELAPA

2013 ◽  
Vol 2 (1) ◽  
pp. 21-25
Author(s):  
Jhon Peri Rinaldo Sirait ◽  
Nico Sihombing ◽  
Zuhrina Masyithah
Keyword(s):  
Base Material ◽  
Sodium Bisulfite ◽  
Coconut Shell ◽  
Effect Of Temperature ◽  
Agitation Rate ◽  
Reactant Ratio ◽  
Ir Spectrophotometry ◽  
Ft Ir ◽  
Coconut Shell Powder ◽  
Shell Powder

Coconut shell is one of agricultural wastes that having low commercial value. This research is objected to use coconut shell as the base material of producing surfactant. The use of coconut shell is basically due to its content of lignin, about 29,4%. The objective of this research is to obtain isolate lignin with increasing chatalis NaOH and H2SO4 with lignin identification, the effect of temperature and agitation rate of producing surfactant. The research was done in a reactor with temperature of 100 0C, 110 0C, 120 0C, 3 hours reaction time, pH 6, 80 rpm, 90 rpm, 100 rpm agitation rate, and coconut shell as the base material. Dry coconut shell is grinded and the powder is collected to be reacted. The coconut shell powder is reacted with sodium bisulfite solution with variation in ratio of 1:0,5.  The product is filtered to get filtrate and residue. The filtrate is further analyzed by using the FT-IR spectrophotometry method. From the research we get maximum purity of surfactant at sodium bisulfite with reactant ratio of 1:0,5;  Speed 100 rpm and temperature 120 0C.

Synthesis N-palmitoyl lysine from palmitate acid and L-lysine used mixed solvent: Effect of temperature and reaction time

2019 ◽  
Author(s):  
M. Syukri ◽  
N. R. Purba ◽  
B. R. Hutajulu ◽  
D. Alfizah ◽  
A. Hutagalung ◽  
...  
Keyword(s):  
Reaction Time ◽  
Solvent Effect ◽  
Mixed Solvent ◽  
Effect Of Temperature

scholarly journals MODEL KINETIKA EKSTRAKSI FLAVONOID DARI BAYAM MERAH (Alternanthera amoena voss)

2018 ◽  
Vol 6 (4) ◽  
pp. 8-14
Author(s):  
Iriany ◽  
Irsa Septiawan ◽  
Salwa Jody Gustia
Keyword(s):  
Mass Transfer ◽  
Transfer Coefficient ◽  
Mass Transfer Coefficient ◽  
Total Content ◽  
Effect Of Temperature ◽  
Polyphenol Compounds ◽  
Water Solvent ◽  
Ir Spectrophotometry ◽  
Ft Ir

Red spinach (Alternanthera amoena voss) contains vitamins, protein, and flavonoids. Flavonoid is polyphenol compounds having properties as a free radical catcher.The purpose of this research is to obtain the kinetic rate of flavonoid mass transfer from red spinach.Extraction is one of the way to take flavonoids contained in solids with the assist of solvents. Mass transfer in liquid solid extraction occurs by diffusion. The determination of mass transfer coefficient (KC) is to conduct the rate of mass transfer of flavonoids from solids. In this study, the effect of temperature on the extraction of flavonoids from red spinach with water solvent is observed. The temperatures extraction in this research are of 50°C, 60°C, and 70°C respectively. Determinationof total flavonoid, mass transfer coefficient, and antioxidant activity carried out using FT-IR Spectrophotometry and UV-VIS Spectrophotometry. This study concluded that the increase in extraction time and temperature will increase the total content of flavonoids and extract rendement.Mass transfer coefficient equation in this study is K = 3078645 . Antioxidants in red spinach are included in the group of very strong antioxidants.

scholarly journals OPTIMASI SINTESIS BIOSURFAKTAN LAURIL AMIDA DARI ASAM LAURAT DAN DIETANOLAMINA MENGGUNAKAN PELARUT HEXANE DAN ENZIM LIPASE TERIMOBILISASI

2017 ◽  
Vol 6 (2) ◽  
pp. 19-23
Author(s):  
Denny Samuel Silaen ◽  
Tjahjono Herawan ◽  
Zuhrina Masyithah ◽  
Hiskia Arapenta Ginting
Keyword(s):  
Lauric Acid ◽  
Acid Value ◽  
Enzyme Concentration ◽  
Solvent Ratio ◽  
Filtration Method ◽  
Amide Synthesis ◽  
Novozyme 435 ◽  
Amidation Reaction ◽  
Percent Conversion ◽  
Substrate Ratio

Lauril amide is one of nonionic surfactant and has potency to become an ecofriendly surfactant. The main problem on lauril amide synthesis is the low conversion of lauric acid. Optimation of lauril amide synthesis is done with three variabels which give influence of amidation reaction. One stage amidation was done by reacting lauric acid with diethanolamine using catalyst Novozyme 435® with substrate ratio lauric acid:diethanolamine 1:1; 2:1; 3:1; 4:1; 5:1, amount of catalyst 1,8; 4; 7; 10; 11,8% from lauric acid total amount, solvent ratio 0; 1:1; 2:1; 3:1; 4:1 from lauric acid total amount and reacted for 24 hours with temperature reaction 55oC and 500 rpm. Product is separated from catalyst using filtration method and then purified by washing with acetone and heated at temperature of 90 oC to remove solvent. Product has been analyzed with acid value to obtained percent conversion of lauril amide, determine of Hydrophilic Liphophilic Balance value, spectroscopy Fourier Transform Infrared and determine of critical micelle concentrasion. Percent conversion optimum has obtained 86,16% at condition substrate ratio 1:1, enzyme concentration Novozyme 435® 7% and solvent ratio 2:1. Analysis result of lauril amide surfactant gave the hidrophile liphophile balance value about 11,93, it means that lauril amide surfactant can be used as emultion oil in water.

Authentication of the Ancient Easel / Paintings Through Materials Identification from the Polychrome Layers II. Analysis by Means of the FT-IR Spectrophotometry

2008 ◽  
Vol 59 (4) ◽  
Author(s):  
Irina Crina Anca Sandu ◽  
Constantin Luca ◽  
Ion Sandu ◽  
Viorica Vasilache ◽  
Mikiko Hayashi
Keyword(s):  
Degradation Rate ◽  
Animal Glue ◽  
Painting Materials ◽  
Ageing Rate ◽  
Ir Spectrophotometry ◽  
Private And Public ◽  
Ft Ir

This is the second paper belonging to a study concerning the authentication of ancient easel-paintings, on canvas and wood support, from private and public collections, by using the FT-IR spectrophotometry technique for the analysis of the painting materials. Different pigments, egg binders, caseins and animal glue, often found in ancient easel-paintings on wood or canvas, have been used as standards for establishing the ageing rate of the paintings by correlation with the dates presented in the first note. The determination of the degradation rate of the painting materials is an important archaeometric characteristic used in authentication.

scholarly journals Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mohammad Hossein Abdollahi-Basir ◽  
Boshra Mirhosseini-Eshkevari ◽  
Farzad Zamani ◽  
Mohammad Ali Ghasemzadeh
Keyword(s):  
Ionic Liquid ◽  
Catalytic Activity ◽  
Reaction Time ◽  
Metal Organic Framework ◽  
One Pot ◽  
Short Reaction Time ◽  
Three Component Reaction ◽  
Metal Organic ◽  
Ft Ir ◽  
Novel Catalyst

AbstractA one-pot three component reaction of benzaldehydes, 1H-tetrazole-5-amine, and 3-cyanoacetyl indole in the presence of a new hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal–organic framework as a recyclable catalyst was explored. This novel catalyst, which was fully characterized by XRD, FE-SEM, EDX, FT-IR, TGA, BET, and TEM exhibited outstanding catalytic activity for the preparation of a range of pharmaceutically important tetrazolo[1,5-a]pyrimidine-6-carbonitriles with good to excellent yields in short reaction time.

scholarly journals Clinoptilolite as a natural, active zeolite catalyst for the chemical transformations of geraniol

2021 ◽  
Author(s):  
Anna Fajdek-Bieda ◽  
Agnieszka Wróblewska ◽  
Piotr Miądlicki ◽  
Jadwiga Tołpa ◽  
Beata Michalkiewicz
Keyword(s):  
Reaction Time ◽  
Nitrogen Adsorption ◽  
Carbon Chain ◽  
Raw Material ◽  
Chemical Transformations ◽  
Renewable Biomass ◽  
Ft Ir ◽  
Catalyst Content ◽  
Favorable Conditions ◽  
Instrumental Methods

AbstractThis work presented the studies with the natural zeolite—clinoptilolite as the catalyst for the isomerization of geraniol. During the research, it turned out that the studied process is much more complicated, and not only isomerization takes place in it, but also dehydration, oxidation, dimerization, cyclization and fragmentation of the carbon chain. Geraniol is an organic raw material which can be obtained not only by a chemical synthesis but also from plants (renewable biomass) by distillation or extraction method, for example a source of geraniol can be a plant—geranium. Before catalytic tests clinoptilolite was characterized by the instrumental methods, such as: XRD, porosity studies—nitrogen adsorption at 77 K, SEM, EDXRF, and FT-IR. Gas chromatography analyses showed that the main products of geraniol isomerization process were 6,11-dimethyl-2,6,10-dodecatrien-1-ol and thumbergol. The selectivity of 6,11-dimethyl-2,6,10-dodecatrien-1-ol and thumbergol depended on the temperature, catalyst content and reaction time. These parameters were changed in the following ranges: 80–150 °C (temperature), 5–15 wt% (catalyst content) and 15–1440 min. (reaction time). The most favorable conditions for 6,11-dimethyl-2,6,10-dodecatrien-1-ol and thumbergol obtaining were: temperature 140 ºC, catalyst content 12.5 wt% and reaction time 180 min. At these conditions, the conversion of geraniol amounted to 98 mol%, and the selectivities of 6,11-dimethyl-2,6,10-dodecatrien-1-ol and thumbergol amounted to 14 and 47 mol%, respectively.

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