Marwa F. Abdul Jabbar, Abdulkareem Dahash Affat, Luay Badr Hamad
{"title":"Transesterification of Waste Cooking Oil Using Natural and Chemical Materials as Catalyst","authors":"Marwa F. Abdul Jabbar, Abdulkareem Dahash Affat, Luay Badr Hamad","doi":"10.4028/p-EnBm0E","DOIUrl":"https://doi.org/10.4028/p-EnBm0E","url":null,"abstract":"Due to the greenhouse effect of increased fossil fuel use, resulting in an increase in the period during which fossil fuels will remain available. Because of its advantages for the environment and its production from renewable resources, biodiesel has grown more appealing. As there is a supply of used cooking oil, interest in producing biodiesel is rising. This research examines how CaO and sawdust function as heterogeneous catalysts in transesterification regarding ethanol to produce bio-diesel from the used cooking oil. The impacts of the subsequent variables on the yield of the created biodiesel were investigated. Those parameters include the catalyst concentration (0.5-3 wt%), reaction period (1-4 hr), the molar ratio of ethanol to oil (8:1– 20:1), and temperature (45 to 80 °C). This led to the discovery that CaO catalyst is more efficient compared to the sawdust catalyst, with the maximum percentage yield being 75% for the sawdust catalyst and 95% for the CaO catalyst under catalyst conditions (0.50%), ethanol oil molar ratio of 20:1, and 65 Celsius temperature for 3 hours. It was evident from the results that the biodiesel fuel produced by the catalyst developed in this study fell within the acceptable range of biodiesel fuel.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86861236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Samer Abdulridha, A. Radhi, Marwa N. Abbas, Amal K. Shehab, Wisam M. Aluaibi
{"title":"Maximizing High Value Light Products by Catalytic Cracking of VGO Produced by Iraqi Refinery over Formulated FCC Catalyst","authors":"Samer Abdulridha, A. Radhi, Marwa N. Abbas, Amal K. Shehab, Wisam M. Aluaibi","doi":"10.4028/p-kL6QSL","DOIUrl":"https://doi.org/10.4028/p-kL6QSL","url":null,"abstract":"Prototype of FCC catalyst were formulated by mixing the stabilised Y zeolites (68wt%) with polyvinal alcohol (PVA) (7%) as a solution binder and bentonite (25%). The Y zeolite including the original HY with Si/Al of 2.6 (cat.-2.6) and dealuminated HY with Si/Al of 30 (cat.-30) were used and tested for catalytic cracking of Iraqi vacuum gas oil (VGO) obtained from Al-Dura refinery using a pilot plant. The cracking process was carried out at a temperature of 520 °C and atmospheric pressure, The weight ratio of catalyst / oil ratio was 3 and 5. The results show that higher conversion of 77 wt. % and better product distribution (gasoline, kerosene and gas oil) could be obtained over cat.30 resulting to a good liquid product yield. The catalytic activity, in terms of VGO conversion was not affected over cat.-30 in spite of its lower acidity, suggesting the determinate of mesoporosity in the Y zeolite (cat.-30) catalysed cracking reactions. A higher yield of ~ 67 wt% to mid-distillates (i.e.Naphtha and kerosene) was as a result of the improvements in the diffusion to and from catalyst structure.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72554649","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Studying the Factors Affecting De-Emulsification of Crude Oil","authors":"Zolfa Q. Atshan, M. A. Mohammed","doi":"10.4028/p-aYNBt6","DOIUrl":"https://doi.org/10.4028/p-aYNBt6","url":null,"abstract":"The paper deals with highly stable emulsions. It is concentrated on de-emulsification of crude oil. In the petroleum industry, de-emulsification is an important and urgent task that is typically required for the treatment of crude oil. This work, suggests method using coupling device integrated centrifuge with chemical to strengthen the de-emulsification efficiency. A number of de-emulsification runs were conducted to determine how centrifuge and chemical components affected the effectiveness of de-emulsifying crude oil and the separation of water, Different types of de-emulsifiers the (ethylene glycol, choline chloride and ethyl cellulose), were used with different concentration of de-emulsifiers, de-emulsification time in centrifuge and centrifugal speed. Also studied at the same time. Studies on the de-emulsification of crude oil were conducted at room temperature. As the concentration of de-emulsifiers was increased, crude oil's de-emulsification efficiency rose , centrifuge time and centrifugal speed ,with de-emulsifier type effect on de- emulsification ,which reached maximum (85.9%,84.4% and 74.07%) at rate 4% of ethylene glycol, choline chloride and ethyl cellulose respectively ,at 60 min and 4000 rpm . This method provides higher water separation from crude oil emulsion and quicker method.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74245939","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Susi, M. Ainuri, W. Wagiman, M. Affan, Fajar Falah
{"title":"Depolymerization of Cellulose Components from Oil Palm Empty Fruit Bunches in Bleaching and Delignification Process","authors":"S. Susi, M. Ainuri, W. Wagiman, M. Affan, Fajar Falah","doi":"10.4028/p-ugJQs1","DOIUrl":"https://doi.org/10.4028/p-ugJQs1","url":null,"abstract":"Oil palm empty fruit bunches (OPEFB) are oil palm industry waste which is indeed abundant. OPEFB waste has been explorated to make fiber, cellulose, and its derivatives. In the process of extracting cellulose, there is depolymerization of several components, both hemicellulose, lignin, color, and structural elements. The combination of bleaching under acidic conditions and alkaline delignification gave different changes, one of which depends on the type of bleacher, concentration, reaction time, and the number of stages carried out. This study aimed to examine the effect of NaClO2 concentration and bleaching time on the physical and chemical characteristics that indicate the depolymerization process of OPEFB fiber. Depolymerization can be indicated by changes in the cellulose color, the content of cellulose, and the changes in cellulose crystallinity. The change of cellulose mass was affected by the bleacher concentration and the bleaching time. High concentrations of bleacher will reduce the cellulose mass significantly. Similarly, the depolymerization of the chromophore elements in OPEFB fiber will show a change in color from brown to gray-white with different brightness intensities. The XRD test indicated that there was a correlation between low crystallinity with the use of high bleacher concentrations.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80993188","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Review: Membrane Reactor for Hydrogen Production: Modeling and Simulation","authors":"Alaa Hasan Kassi, T. Al-Hattab","doi":"10.4028/p-XakNe1","DOIUrl":"https://doi.org/10.4028/p-XakNe1","url":null,"abstract":"A membrane reactor is a multifactional vessel used for H2 production. Hydrogen's three spectrum colors are dependent on carbon present. Two types of membrane with high permeability to hydrogen (polymeric and metallic) Hydrogen is produced in two systems: conventional reactors and membrane reactors (which separate and purify hydrogen in a single vessel). There are many types of membrane reactors according to design (catalytic membrane reactor (CMR), fixed bed reactor (FBMR), fluidized bed reactor (FBMR), etc. The transport mechanism of H2 through the membrane by a \"sorption-diffusion mechanism\" and the government equations that are used for membrane reactor modeling and simulation, such as continuity, momentum, mass, and heat transfer equations of the CMR, and the thickness of the membrane. These equations are solved by MATLAB, COMSOL, and the Finite Element Method to simulate the MR at different parameters: rate of conversion, rate of sweep gas, temperature, pressure, rate of H2 permeation through a membrane, and activity of the catalyst. We summarized theoretical studies for membrane reactors, including the operation conditions, type of hydrocarbon feed, type of production method, kind of catalyst, and heat effect.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86192650","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
T. Q. Toan, T. Dinh, T. Tran, Thi Bich Hoang, Q. Pham, Quyet Chien Nguyen, N. N. Quy, Thanh Viet Nguyen
{"title":"Chemical Compositions of Essential Oil of Agarwood (Aquilaria crassna) Harvested in Phu Quoc Island, Vietnam","authors":"T. Q. Toan, T. Dinh, T. Tran, Thi Bich Hoang, Q. Pham, Quyet Chien Nguyen, N. N. Quy, Thanh Viet Nguyen","doi":"10.4028/p-oHM1mQ","DOIUrl":"https://doi.org/10.4028/p-oHM1mQ","url":null,"abstract":"The importance of natural products derived from Agarwood species is increasingly emphasized in the production of perfumery or cosmetic products made on Agarwood species. On the other hand, due to the predominant amount of aromatic compounds in essential oils, frankincense essential oil is increasingly popular with high economic value. Therefore, in this study, we focused on the extraction process of essential oils and evaluated the chemical composition present in the essential oils by the GC-MS method. Differences in the composition of essential oils between natural and artificial agarwood may be due to species, habitat conditions, climate, geographical conditions, and extraction methods in different regions. Specifically, volatile components in essential oils were identified as Neopetasone (14.43%); Dihydroagarofuran-15-al (9.20%); Jinko-cramol (5.02%); Valeriano (4.94%); Agarofuran (8.02%); Dihydrokaranone (3.25%), Valenca-1 (10), 8-dien-11-ol (5.95%) and Selina-4,11-dien-14-al (2.73%), contribute to determining the main aroma in Agarwood essential oil.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72409682","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
I. Sudaryadi, F. Oktaweni, I. E. Pramono, K. W. Fatikasary, H. Widiawati, S. Sutikno
{"title":"Propolis Bioactive Compounds of Stingless Bees (Tetragonula laeviceps) from Mount Merapi Slope, Sleman, Yogyakarta","authors":"I. Sudaryadi, F. Oktaweni, I. E. Pramono, K. W. Fatikasary, H. Widiawati, S. Sutikno","doi":"10.4028/p-g9Eic6","DOIUrl":"https://doi.org/10.4028/p-g9Eic6","url":null,"abstract":"The emergence of many new diseases due to viruses and bacteria demands for an increase in the discovery of natural alternative medicines. One example of sources of natural medicine is the honey and the propolis of Tetragonula laeviceps bee. The efficacy, physical and chemical properties of honey are known to be influenced by the type of pollen and the environment whilst the composition of propolis is influenced by the geological factors. Therefore, the purpose of this research was to study the composition of propolis’ bioactive compounds of T.laeviceps bee from Mount Merapi Slope, Sleman, Yogyakarta. The bioactive compound composition of the propolis sample were analysed by Gas Chromatograph-Mass Spectrometry (GC-MS). The analysis showed that the propolis has various type of compounds containing up to 20 bioactive compounds which can be classified in three different groups namely alkaloids (70%), phenolics (20%), and terpenoids (5%). Most of these compounds were found to be biologically important. However, further research is still required to confirm the potential antimicrobial properties of the propolis’ bioactive compounds.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81593677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Synthesis and Characterization of Carbonate Hydroxyapatite from Pinctada Maxima Shell with Short Aging Time for Bone Biomaterial Candidate","authors":"M. Megawati, D. J. Patty, Y. Yusuf","doi":"10.4028/p-08k84g","DOIUrl":"https://doi.org/10.4028/p-08k84g","url":null,"abstract":"Biomaterial products for bone repair are needed to support accelerated tissue healing. This research aimed to synthesize and characterize carbonate hydroxyapatite (CHA) from Pinctada maxima (P. maxima) using the precipitation method with a short aging time, 15 min. CHA was dried with oven-dry at 100°C for 12 h (CHA A) and a furnace-dry at 1000°C for 2 h (CHA B). Short aging time succeeded in producing CHA B-type with lattice parameters and of CHA A is 9.382 and 6.964 , while 9.451 and 6.962 for CHA B. The high temperature treatment made the diffraction peak indicating CHA more detected and crystallinity increased to 97.87%. The appearance of C–O bond and diffraction peaks of CHA verified substituted carbonates hydroxyapatite.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84986314","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Synthesis, Characterization, Optical and Luminescence Properties of Copper Based Metal Organic Frame Works","authors":"Maya Pai, V. Adimule, B. Yallur, S. Batakurki","doi":"10.4028/p-533xs2","DOIUrl":"https://doi.org/10.4028/p-533xs2","url":null,"abstract":"Herein, we report synthesis of two new copper metal organic frameworks. The organic linkers were terephthalic acid with 6-Dihydroimidazo[2,1-b]thiazole-2-carbaldehyde and terephthalic acid with 3-benzothiazol-2-yl-malonaldehyde used in the copper nano metal organic framework (MOF). Both the Cu-MOF’s were characterized by XRD, UV-vis spectroscopy and FTIR. XRD crystallographic studies revealed the presence of copper metal at 2θ at 18.4°. Tauc plots were simulated to calculate the band gap of both Cu-MOF’s and result indicated the band gap energy of Cu-MOF 1 at 3.31 eV and for Cu-MOF 2 was at 3.57 eV. The UV-Visible absorption studies indicated two bands for Cu-MOF 1 and Cu-MOF 2 at 326 nm. However, the second band in Cu MOF 1 at 509 nm was slightly shifted to higher wavelength at 516 nm in Cu-MOF 2 due to the extension of π-π* transition. The photoluminescent properties of both Cu-MOF’s indicated a strong band at 505 nm. Thus, the optical properties of both the Cu-MOF’s infers that these can be a promising semiconductor material for various electronic applications.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88053702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Michael Sean P. Deang, Jayke Matthew Fajardo, David Tañá, T. Tumolva
{"title":"Kinetics Modelling of Vitamin B12 Release in an Agar/κ-Carrageenan Hydrogel Blend","authors":"Michael Sean P. Deang, Jayke Matthew Fajardo, David Tañá, T. Tumolva","doi":"10.4028/p-9cv3vh","DOIUrl":"https://doi.org/10.4028/p-9cv3vh","url":null,"abstract":"A phycocolloidal hydrogel patch is studied as a potential material for the transdermal delivery device for vitamin B12. The vitamin release kinetics from an agar/κ-carrageenan hydrogel blend as a function of mass ratio and vitamin loading. Concentration measurements were done using a colorimetric method, and the experimental data were fitted into the Korsmeyer-Peppas model, Peppas-Sahlin model, and Berens-Hopfenberg model. From the curve fitting, parameters such as first-order polymer relaxation constant and diffusivity constant were obtained. The results showed that for the Korsmeyer-Peppas model and the Peppas-Sahlin model, the release mechanism followed Fickian diffusion predominantly. On the other hand, the Berens-Hopfenberg model fit shows that the release mechanism predominantly follows non-Fickian diffusion and may need to be modified.","PeriodicalId":50368,"journal":{"name":"Industrial and Engineering Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87907381","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}