scholarly journals EKSTRAKSI ASAM SITRAT DAN ASAM OKSALAT : PENGARUH TRIOCTYLAMINE SEBAGAI EXTRACTING POWER DALAM BERBAGAI SOLVEN CAMPURAN TERHADAP KOEFISIEN DISTRIBUSI

REAKTOR ◽  
2008 ◽  
Vol 12 (2) ◽  
pp. 107
Author(s):  
Mega Kasmiyatun ◽  
Bakti Jos

Generally, liquid waste of citric acid industry containing a highly citric acid, oxalic acid, due to precipitation process of calcium citrate less completely. Liquid-liquid extraction process is this one alternative that used to recover citric acid and oxalic acid, either in the product separation process from the fermentor or the treatment of its liquid waste. In order to understand, that the extraction process can be applied both technically and economically, it needs a more study the extraction parameters. The investigation has carried out about study of the extraction of citric acid and oxalic acid used trioctyl-amine as extracting power on various mix solvent and its ratio, related to the distribution coefficient. Extraction used a separating funnel that it was shaked with using an automatic shaker, which adjusted on specific velocity during 2.5 hours. The rafinate and extract were separated by separating funnel, then they were analyzed both concentration of citric acid and oxalic acid using a high performance liquid chromatography (HPLC). The results of the research show that the mixed solvent (consist of 15% trioctyl amine, 70% dodecane, and 15% hexanol), for the extraction of citric acid  produce both the highest distribution coefficient and percentage of separation were 1.15 and 74.22%, respectively; and this were achieved for the ratio between the solvent and diluent of 2.5:1. For the extraction of oxalic acid similar result were obtained, and the value were 3.78 and 88.31%, respectively, for the ratio between solvent and diluent of 2:1.Limbah cair pabrik asam sitrat pada umumnya mengandung asam sitrat, asam oksalat, cukup tinggi akibat proses pengendapan calsium sitrat yang kurang sempurna. Proses ekstraksi cair-cair adalah salah satu alternatif yang dapat digunakan untuk pengambilan kembali asam sitrat dan asam oksalat, baik pada proses pemisahan produk yang keluar dari fermentor maupun pada proses pengolahan limbah cairnya. Untuk mengetahui apakah proses ekstraksi dapat diterapkan secara teknis, maka perlu dilakukan pengkajian lebih mendalam parameter-parameter ekstraksi. Pada penelitian ini telah dilakukan pengkajian tentang ekstraksi asam sitrat dan asam oksalat dengan menggunakan trioctylamine sebagai extracting power pada bermacam solven campuran dan pada berbagai perbandingan, hubungannya dengan koefisien distribusinya. Ekstraksi pada berbagai kondisi rancangan percobaan dilakukan pada corong pemisah, yang penggojokannya dilakukan dengan bantuan automatic shaker yang di set pada kecepatan tertentu selama 2,5 jam. Rafinat dan ekstrak dipisahkan selanjutnya dianalisis kadar asam sitrat maupun asam oksalat dengan menggunakan HPLC. Hasil penelitian menunjukkan bahwa solven campuran (yang terdiri dari 15% trioctylamine, 70% dodecane dan 15% hexanol) menghasilkan koefisien distribusi dan persentase pemisahan solute berturut-turut untuk asam sitrat 1,15 dan 74,22% pada perbandingan solven dan diluen 2,5:1; sedang untuk ekstraksi asam oksalat sebesar 3,78 dan 88,31% pada perbandingan solven dan diluen 2:1. 

2011 ◽  
Vol 396-398 ◽  
pp. 1475-1479
Author(s):  
Da Wei Li ◽  
Liang Wu Bi ◽  
Zhen Dong Zhao ◽  
Dong Mei Li ◽  
Yan Gu ◽  
...  

A study to track and detect the variation of bioactive components in rosemary extraction solution and extracts, by adding organic acid synergists, such as citric acid, oxalic acid and tartaric acid, was performed using high performance liquid chromatography (HPLC). Ultrasound was also used to increase the extraction efficiency, improve the yields of rosemary extracts and shorten the extraction time. The experimental results showed that the content of the key bioactive component carnosic acid was easier to reduce during the storage of extraction solution and extracts, meanwhile, adding citric acid, oxalic acid and tartaric acid during the extraction could actually slow down the trend of the reduction of the bioactive components, especially for carnosic acid.


TAPPI Journal ◽  
2012 ◽  
Vol 11 (8) ◽  
pp. 17-24 ◽  
Author(s):  
HAKIM GHEZZAZ ◽  
LUC PELLETIER ◽  
PAUL R. STUART

The evaluation and process risk assessment of (a) lignin precipitation from black liquor, and (b) the near-neutral hemicellulose pre-extraction for recovery boiler debottlenecking in an existing pulp mill is presented in Part I of this paper, which was published in the July 2012 issue of TAPPI Journal. In Part II, the economic assessment of the two biorefinery process options is presented and interpreted. A mill process model was developed using WinGEMS software and used for calculating the mass and energy balances. Investment costs, operating costs, and profitability of the two biorefinery options have been calculated using standard cost estimation methods. The results show that the two biorefinery options are profitable for the case study mill and effective at process debottlenecking. The after-tax internal rate of return (IRR) of the lignin precipitation process option was estimated to be 95%, while that of the hemicellulose pre-extraction process option was 28%. Sensitivity analysis showed that the after tax-IRR of the lignin precipitation process remains higher than that of the hemicellulose pre-extraction process option, for all changes in the selected sensitivity parameters. If we consider the after-tax IRR, as well as capital cost, as selection criteria, the results show that for the case study mill, the lignin precipitation process is more promising than the near-neutral hemicellulose pre-extraction process. However, the comparison between the two biorefinery options should include long-term evaluation criteria. The potential of high value-added products that could be produced from lignin in the case of the lignin precipitation process, or from ethanol and acetic acid in the case of the hemicellulose pre-extraction process, should also be considered in the selection of the most promising process option.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Robert Christie

Abstract This paper presents an overview of the general chemical principles underlying the structures, synthesis and technical performance of azo pigments, the dominant chemical class of industrial organic pigments in the yellow, orange, and red shade areas, both numerically and in terms of tonnage manufactured. A description of the most significant historical features in this group of pigments is provided, starting from the discovery of the chemistry on which azo colorants are based by Griess in the mid-nineteenth century, through the commercial introduction of the most important classical azo pigments in the early twentieth century, including products known as the Hansa Yellows, β-naphthol reds, including metal salt pigments, and the diarylide yellows and oranges, to the development in the 1950s and 1960s of two classes of azo pigments that exhibit high performance, disazo condensation pigments and benzimidazolone-based azo pigments. A feature that complicates the description of the chemical structures of azo pigments is that they exist in the solid state as the ketohydrazone rather than the hydroxyazo form, in which they have been traditionally been illustrated. Numerous structural studies conducted over the years on an extensive range of azo pigments have demonstrated this feature. In this text, they are referred to throughout as azo (hydrazone) pigments. Since a common synthetic procedure is used in the manufacture of virtually all azo (hydrazone) pigments, this is discussed in some detail, including practical aspects. The procedure brings together two organic components as the fundamental starting materials, a diazo component and a coupling component. An important reason for the dominance of azo (hydrazone) pigments is that they are highly cost-effective. The syntheses generally involve low cost, commodity organic starting materials and are carried out in water as the reaction solvent, which offers obvious economic and environmental advantages. The versatility of the approach means that an immense number of products may be prepared, so that they have been adapted structurally to meet the requirements of many applications. On an industrial scale, the processes are straightforward, making use of simple, multi-purpose chemical plant. Azo pigments may be produced in virtually quantitative yields and the processes are carried out at or below ambient temperatures, thus presenting low energy requirements. Finally, provided that careful control of the reaction conditions is maintained, azo pigments may be prepared directly by an aqueous precipitation process that can optimise physical form, with control of particle size distribution, crystalline structure, and surface character. The applications of azo pigments are outlined, with more detail reserved for subsequent papers on individual products.


Inventions ◽  
2021 ◽  
Vol 6 (3) ◽  
pp. 50
Author(s):  
Silvia Lazăr (Mistrianu) ◽  
Oana Emilia Constantin ◽  
Nicoleta Stănciuc ◽  
Iuliana Aprodu ◽  
Constantin Croitoru ◽  
...  

(1) Background: This study is designed to extract the bioactive compounds from beetroot peel for future use in the food industry. (2) Methods: Spectrophotometry techniques analyzed the effect of conventional solvent extraction on betalains and polyphenolic compounds from beetroot peels. Several treatments by varying for factors (ethanol and citric acid concentration, temperature, and time) were applied to the beetroot peel samples. A Central Composite Design (CCD) has been used to investigate the effect of the extraction parameters on the extraction steps and optimize the betalains and total polyphenols extraction from beetroot. A quadratic model was suggested for all the parameters analyzed and used. (3) Results: The maximum and minimum variables investigated in the experimental plan in the coded form are citric acid concentration (0.10–1.5%), ethanol concentration (10–50%), operating temperature (20–60 °C), and extraction time (15–50 min). The experimental design revealed variation in betalain content ranging from 0.29 to 1.44 mg/g DW, and the yield of polyphenolic varied from 1.64 to 2.74 mg/g DW. The optimized conditions for the maximum recovery of betalains and phenols were citric acid concentration 1.5%, ethanol concentration 50%, temperature 52.52 °C, and extraction time 49.9 min. (4) Conclusions: Overall, it can be noted that the extraction process can be improved by adjusting operating variables in order to maximize the model responses.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Xuemei Ma ◽  
Jiayi Yu ◽  
Jing Jing ◽  
Qian Zhao ◽  
Liyong Ren ◽  
...  

AbstractPectin is a kind of natural and complex carbohydrates which is extensively used in food, chemical, cosmetic, and pharmaceutical industries. Fresh sunflower (Helianthus annuus L.) heads were utilized as a novel source of pectin extracted by ammonium oxalate. The conditions of the extraction process were optimized implementing the response surface methodology. Under optimal extraction parameters (extraction time 1.34 h, liquid–solid ratio 15:1 mL/g, ammonium oxalate concentration 0.76% (w/v)), the maximum experimental yield was 7.36%. The effect of spray-drying and freeze-drying on the physiochemical properties, structural characteristics, and antioxidant activities was investigated by FT-IR spectroscopy, high performance size exclusion chromatography, and X-ray diffraction. The results showed freeze-drying lead to decrease in galacturonic acid (GalA) content (76.2%), molecular weight (Mw 316 kDa), and crystallinity. The antioxidant activities of pectin were investigated utilizing the in-vitro DPPH and ABTS radical-scavenging systems. This study provided a novel and efficient extraction method of sunflower pectin, and confirmed that different drying processes had an effect on the structure and properties of pectin.


Pharmaceutics ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 1008 ◽  
Author(s):  
Qilei Yang ◽  
Chang Zu ◽  
Wengang Li ◽  
Weiwei Wu ◽  
Yunlong Ge ◽  
...  

Paclitaxel (PTX) is a poor water-soluble antineoplastic drug with significant antitumor activity. However, its low bioavailability is a major obstacle for its biomedical applications. Thus, this experiment is designed to prepare PTX crystal powders through an antisolvent precipitation process using 1-hexyl-3-methylimidazolium bromide (HMImBr) as solvent and water as an antisolvent. The factors influencing saturation solubility of PTX crystal powders in water in water were optimized using a single-factor design. The optimum conditions for the antisolvent precipitation process were as follows: 50 mg/mL concentration of the PTX solution, 25 °C temperature, and 1:7 solvent-to-antisolvent ratio. The PTX crystal powders were characterized via scanning electron microscopy, Fourier transform infrared spectroscopy, high-performance liquid chromatography–mass spectrometry, X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, Raman spectroscopy, solid-state nuclear magnetic resonance, and dissolution and oral bioavailability studies. Results showed that the chemical structure of PTX crystal powders were unchanged; however, precipitation of the crystalline structure changed. The dissolution test showed that the dissolution rate and solubility of PTX crystal powders were nearly 3.21-folds higher compared to raw PTX in water, and 1.27 times higher in artificial gastric juice. Meanwhile, the bioavailability of PTX crystal increased 10.88 times than raw PTX. These results suggested that PTX crystal powders might have potential value to become a new oral PTX formulation with high bioavailability.


RSC Advances ◽  
2016 ◽  
Vol 6 (54) ◽  
pp. 49228-49235 ◽  
Author(s):  
Chengwei Gao ◽  
Baojun Li ◽  
Ning Chen ◽  
Jie Ding ◽  
Qiang Cai ◽  
...  

Fe3O4/HNT@rGO composite (FHGC) was fabricated via a facile co-precipitation process, followed by heat treatment. For RhB and As5+removal, the high performance and easy separation of FHGC highlight its potential application in water treatment.


2013 ◽  
Vol 15 (3) ◽  
pp. 81-84 ◽  
Author(s):  
Indrasing D. Patil ◽  
Yogita S. Patil ◽  
Bhausaheb L. Pangarkar

Abstract Pesticide pollution is a serious problem being faced. Harmful levels of pesticides are found in the water which is used for daily purposes. In the event of such a scenario, this paper presents a working solution for bringing down the Pesticide levels in the water to safe levels by using the method of liquid-liquid extraction. The experimental liquid-liquid equilibrium data on pesticide-water-solvent ternary mixtures at a temperature of 288.15 K are presented here. The pesticide used here is a chlorinated hydrocarbon called lindane found in the water (underground, land), beverages and foods. The solvents used are Petro-ether-Chloroform (1:1), Ethylene di chloride and n-hexane. The equilibrium generation diagram, triangular diagram, tie lines and bimodal curves as well as the distribution coefficient have been determined and reported. The petro-ether-chloroform was found to be the right solvent for the separation of lindane from wastewater because of high selectivity (25.36) and distribution coefficient (4). The extraction process is simulated into ‘C’ language


2013 ◽  
Vol 295-298 ◽  
pp. 150-154
Author(s):  
Feng Jie Wang ◽  
Xin Qiao Dong ◽  
Xiao Liu

Development natural pigment retained a variety of nutrition composition is extremely research value.Water Wax Trees Fruit was as raw materials,citric acid aqueous solution was as extracting agent.Amaranthine pigment extraction method were studied on fully grasping the stability of the natural amaranthine pigment and no damage to the water wax fruit biological activity.The effect of extraction yield were studied on Water Wax Trees Fruit natural amaranthine pigment.The results show that the better extraction conditions are extraction temperature at 70 °C, extraction time for 3h,citric acid concentration1.0 % , the material/liquid ration(g/ml) 1:5.The extraction yield is 2.95%.Ultraviolet absorption maximum wavelength is 280 nm.


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