Preparation of Sodium Diacetate

2014 ◽  
Vol 508 ◽  
pp. 79-82
Author(s):  
Jian Wei Zhang ◽  
Ji Wei Liu
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Sodium Hydroxide ◽  
Reaction Temperature ◽  
Orthogonal Experiment ◽  
Product Yield ◽  
Phase Method ◽  
Synthesis Conditions ◽  
Optimum Synthesis ◽  
Sodium Diacetate

The sodium diacetate using acetic acid and sodium hydroxide as materials was prepared in which one-step liquid-phase method and microwave method were adopted in the paper. By single factor experiment, the regularities of the influence of various factors including reaction temperature, reaction time and acetic acid-sodium hydroxide ratio on the yield of sodium diacetate were studied. Through the orthogonal experiment the optimum synthesis conditions of sodium diacetate were confirmed that the reaction temperature was 70°C, the reaction time was 60min and the acetic acid-sodium hydroxide ratio was 2.1:1. The product yield was 96.2% under the optimal reaction conditions.

scholarly journals Optimization of Synthesis of Seleno-Sargassum fusiforme(Harv.) Setch. Polysaccharide by Response Surface Methodology, Its Characterization, and Antioxidant Activity

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Yu-Bin Ji ◽  
Fang Dong ◽  
Miao Yu ◽  
Long Qin ◽  
Dan Liu
Keyword(s):  
Antioxidant Activity ◽  
Response Surface Methodology ◽  
Reaction Time ◽  
Response Surface ◽  
Reaction Temperature ◽  
Sargassum Fusiforme ◽  
Synthesis Conditions ◽  
Optimum Reaction ◽  
Series Of Experiments

The response surface methodology was employed to optimize the synthesis conditions of seleno-Sargassum fusiforme(Harv.) Setch. polysaccharide. Three independent variables (reaction time, reaction temperature, and ratio of Na2SeO3to SFPSI) were tested. Furthermore, the characterization and antioxidant activity of Se-SFPSIin vivowere investigated. The result showed that the actual experimental Se content of Se-SFPSI was 3.352 mg/g at the optimum reaction conditions of reaction time 8 h, reaction temperature 71°C, and ratio of Na2SeO3to SFPSIB 1.0 g/g. A series of experiments showed that the characterization of Se-SFPSIB was significantly different from that of SFPSIB. Additionally, antioxidant activity assay indicated that the Se-SFPSIB could increase catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) activity of mice bearing tumor S180in blood, heart, and liver while decreasing malondialdehyde (MDA) levels. It can be concluded that selenylation is a feasible approach to obtain seleno-polysaccharide which was utilized as highly biological medicine or functional food.

Synthesis and Characterization of a New Phosphorus-Containing Curing Agent PPDTA

2019 ◽  
Vol 953 ◽  
pp. 185-190
Author(s):  
Yong Li Peng ◽  
Ni An Zhuo ◽  
Can Zhang
Keyword(s):  
Infrared Spectroscopy ◽  
Reaction Time ◽  
Reaction Temperature ◽  
Orthogonal Experiment ◽  
Molar Ratio ◽  
Synthesis And Characterization ◽  
Curing Agent ◽  
Phosphorus Containing ◽  
Three Factor

A new phosphorus-containing flame-retardant curing agent PPDTA was synthesized from phenylphosphonic dichloride (PPD) and 3-amino-1,2,4-triazole (TA) in tetrahydrofuran solvent to improve the flame retardancy of epoxy resin. The structure of the compound was analyzed and confirmed by infrared spectroscopy. The effects of reaction time, reaction temperature and ratio of reactants on yield were studied by using three-factor three-level orthogonal experiment. The results show that the yield of PPDTA can reach 86.4%, when the reaction time is 10h, reaction temperature is 70 °Cand the molar ratio of TA to PPD is 2.2:1.

scholarly journals Synthesis and Performance ofN-(Benzoyl) Stearic Acid Hydrazide

2012 ◽  
Vol 9 (2) ◽  
pp. 545-552 ◽  
Author(s):  
Yan-Hua Cai ◽  
Shun-Jiang Li
Keyword(s):  
Reaction Time ◽  
Stearic Acid ◽  
Reaction Temperature ◽  
Orthogonal Experiment ◽  
Acid Hydrazide ◽  
Semiempirical Method ◽  
Molar Ratio ◽  
H Nmr ◽  
And Performance ◽  
Benzoyl Hydrazine

N-(benzoyl) stearic acid hydrazide was synthesized from benzoyl hydrazine and stearyl chloride which was deprived from stearic acid via acylation. The structure of the compound had been characterized by FT-IR,1H NMR, at the same time, the structure of N-(benzoyl) stearic acid hydrazide was optimized by the semiempirical method PM3. The influence of the reaction ratio, reaction time and reaction temperature to the yield ofN-(benzoyl) stearic acid hydrazide was investigated by orthogonal experiment, and the optimized reaction condition was molar ratio of benzoyl hydrazine: stearyl chloride 1:1, reaction time 6 h, reaction temperature 70°C, and the yield was 92.9%. The TGA thermal analysis of N-(benzoyl) stearic acid hydrazide showed that thermal stability ofN-(benzoyl) stearic acid hydrazide was affected by heating rate, and theN-(benzoyl) stearic acid hydrazide enhanced the tensile strength, modulus and elongation at break of Poly(L-lactic acid)(PLLA).

Catalytic Synthesis of Ethyl Acetate Using Ti2SnC

2013 ◽  
Vol 634-638 ◽  
pp. 628-631
Author(s):  
Yun Hui Long ◽  
Jun Ming Guo ◽  
Du Shu Huang ◽  
Gui Yang Liu
Keyword(s):  
Acetic Acid ◽  
Reaction Time ◽  
Ethyl Acetate ◽  
Reaction Temperature ◽  
Conversion Rate ◽  
Reaction System ◽  
Catalytic Performance ◽  
Catalytic Synthesis ◽  
Molar Ratio ◽  
The Ideal

The catalytic synthesis of ethyl acetate from ethanol and acetic acid using Ti2SnC in liquid phase under the atmospheric pressure was studied. The influences of some factors such as catalyst usage, initial reactant molar ratio, reaction temperature and reaction time on acetic acid conversion rate of this reaction system were investigated. The acetic acid conversion rate of 88.12% is achieved while the molar ratio of alcohol and acid is 1:3.6, the amount of catalyst is 0.2000 g, the reaction temperature is 80 °C and the reaction time is 30min. The catalyst Ti2SnC is the ideal catalyst for synthesis of ethyl acetate for good catalytic performance, non-corrosive to equipment, easily separated from product and used repeatedly.

Production of Low Calorie Oil with Enzymatic Catalysis Method

2012 ◽  
Vol 554-556 ◽  
pp. 1178-1182
Author(s):  
Hui Ling Cui ◽  
Yuan Dong Xu ◽  
Yu Jun Zhang ◽  
Hui Bo Song
Keyword(s):  
Reaction Time ◽  
Soybean Oil ◽  
Reaction Temperature ◽  
Orthogonal Experiment ◽  
Enzymatic Catalysis ◽  
Calorific Value ◽  
Molar Ratio ◽  
Reaction Yield ◽  
Low Calorie ◽  
Glycerol Triacetate

The 1, 3-specific lipase of Lipozymetlim was used as catalyst to produce low calorie oil through the reaction of soybean oil with glycerol triacetate. The effects of catalyst using amount, molar ratio of the substrates, reaction temperature and reaction time on the product yields were investigated. The orthogonal experiment results showed that the optimal reaction conditions were the substrate molar ratio of 2:1, reaction temperature of 60 °C, reaction time of 24 h, and 10 % enzyme adding amount per gram of substrate. Under such conditions, the reaction yield was 79.56 %. After 5 times reuse of the enzyme, the yield still could reach 58.94 %. The calorific value of the product was measured by calorimetric method and the value was 35 027 J/g which was about 75 % of the corresponding value for soybean oil.

Synthesis of Butanone 1,2 - Propanediol Ketal by Sulfamic Acid as Catalyzed

2013 ◽  
Vol 781-784 ◽  
pp. 276-279
Author(s):  
Yu Hang Zhao ◽  
Li Cui ◽  
Da Zhi Wang ◽  
Tong Kuan Xu ◽  
Yong Peng Li
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Raw Materials ◽  
Sulfamic Acid ◽  
Product Yield ◽  
Experimental Results ◽  
Reaction Conditions ◽  
Optimal Reaction

Butanone 1,2-propanediol ketal was synthesized by butanone and 1,2-propanediol as raw materials and sulfamic acid as catalyst. The effects of the mole ratio of raw materials agent, the dosage of the water-carrying agent and catalyst, reaction time on the product yield were discussed separately. Experimental results showed that sulfamic acid was a suitable catalyst for synthesizing of butanone 1,2-propanediol ketal. And the optimal reaction conditions are as follows: the mole ratio of butanone to 1,2-propanediol is 1:1.5, the amount of the catalyst is 2.2%, the water-carrying agent is 25ml, the reaction temperature is 358-378K and reaction time 3h. In this condition, the yield of production could reach 93.8%.

scholarly journals A Long-Chain Alkylation of Dialdehyde Starch to Improve Its Thermal Stability and Hydrophobicity

2016 ◽  
Vol 2016 ◽  
pp. 1-7
Author(s):  
Jiang Zhu ◽  
Zhaodong Wang ◽  
Haitao Ni ◽  
Xiang Liu ◽  
Jian Ma ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Reaction Time ◽  
Reaction Temperature ◽  
Orthogonal Experiment ◽  
Raw Material ◽  
Molar Ratio ◽  
Dialdehyde Starch ◽  
Hydrophobic Properties ◽  
Feed Composition ◽  
Long Chain

Hydrophobic dialdehyde starch (HDAS) was synthesized by dialdehyde starch (DAS) and eighteen-alkyl primary amine as the raw material in DMSO. The effect of the reaction conditions on the yield of HDAS was investigated such as catalyst content, reaction temperature, reaction time, and the in-feed molar ratio of -CHO/-NH2. Moreover, the optimized test parameters were obtained by conducting orthogonal experiment. The molecular structure and the morphology of HDAS were characterized via Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). And the thermal stability and the hydrophobic properties of HDAS were investigated by thermal gravimetric analyzer (TG) and the hydrophobic testing. The results indicate that the yield of HDAS is the highest up to 44.21%, with feed composition 1 : 0.9, reaction temperature 40°C, reaction time 8 h, and acetic acid content 3%. And the introduction of the long-chain alkyl groups into the DAS backbones will ameliorate efficaciously the thermal stability and the hydrophobic properties of DAS, which almost has no effect on the DAS particle size.

Resource recovery of waste incineration fly ash: Synthesis of tobermorite as ion exchanger

1999 ◽  
Vol 14 (11) ◽  
pp. 4437-4442 ◽  
Author(s):  
Zhidong Yao ◽  
Chikashi Tamura ◽  
Motohide Matsuda ◽  
Michihiro Miyake
Keyword(s):  
Fly Ash ◽  
Reaction Time ◽  
Sodium Hydroxide ◽  
Hydrothermal Treatment ◽  
Reaction Temperature ◽  
Sodium Hydroxide Solution ◽  
Waste Incineration ◽  
Naoh Solution ◽  
Temperature Time ◽  
Waste Incineration Fly Ash

Tobermorite was synthesized successfully from waste incineration fly ash by hydrothermal treatment in the presence of sodium hydroxide solution. The tobermorite synthesis was examined as a function of reaction temperature, time, and NaOH concentration. The formation of tobermorite was identified in all of the fly ash treated with NaOH at 180 °C, followed by the minor generations of sodalite and cancrinite phases with increasing NaOH concentration and extending reaction time. The NaOH-treated fly ash revealed the uptake behaviors for Cs+ and NH4+, whereas the fly ash untreated with NaOH solution did not show that. The uptake amounts of resulting products were also determined: 0.40 mmol/g for Cs+ and 0.35 mmol/g for NH4+ in the fly ash treated with 2.0 M NaOH at 180 °C for 20 h.

Study on the Separation of Waste Polyester-Cotton Fiber with Dilute Acid

2011 ◽  
Vol 295-297 ◽  
pp. 2088-2091
Author(s):  
Wei Kong ◽  
Yong Ling Yu ◽  
Li Hua Lv
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Cotton Fiber ◽  
Mass Fraction ◽  
Orthogonal Experiment ◽  
Cotton Fibers ◽  
Dilute Acid ◽  
Liquid Ratio ◽  
Priority Order ◽  
Solid Liquid

Process of the separation of waste polyester-cotton fiber with dilute hydrochloric acid was studied. Acid mass fraction, reaction time, reaction temperature and solid-liquid ratio were studied on the effect of separation with the method of Orthogonal experiment. The results showed that the priority order of the factors was reaction time > acid mass fraction > reaction temperature > solid-liquid ratio. The optimal conditions through serious research on such factors were: acid mass fraction 10%, solid-liquid ratio 4g/100ml, reaction temperature 95°Cand reaction time 90 minutes. Through the microscope, polyester and cotton fibers were separated completely in which polyester into fibrous and cotton fibers were hydrolyzed into tiny powder.

A Novel Method of Leaching Vanadium from Extracted Vanadium Residue Using Sodium Sub-Molten Salt Medium

2011 ◽  
Vol 402 ◽  
pp. 253-260
Author(s):  
Lan Jie Li ◽  
Shi Li Zheng ◽  
Dong Hui Chen ◽  
Shao Na Wang ◽  
Hao Du ◽  
...  
Keyword(s):  
Particle Size ◽  
Reaction Time ◽  
Molten Salt ◽  
Reaction Temperature ◽  
Orthogonal Experiment ◽  
Salt Medium ◽  
Leaching Process ◽  
Novel Method ◽  
The Impact ◽  
Leaching Efficiency

Leaching of an extracted vanadium residue in sodium sub-molten salt medium was investigated. The significant effects of reaction temperature, particle size of residue, reaction time and NaOH-to-residue mass ratio on vanadium extraction were studied. By the orthogonal experiment study, it can be concluded that the impact order of factors is Tr> t>R according to the significance to the leaching process. Under conditions of reaction temperature 170°C, NaOH-to-residue 4:1, stirring speed 700 rpm, particle size -74 µm and reaction time around 180 min, leaching efficiency of vanadium obtained is higher than 90%. And, the leaching process of vanadium, with activation energy 27.69 kJ•mol-1, is controlled by the chemical reaction-controlled as the following rate equation. ln(1-x)=-kt

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