scholarly journals Research on the Preparation and Performance of Binary Modified Maltodextrin Water-Reducing Agent

2016 ◽  
Vol 2016 ◽  
pp. 1-6
Author(s):  
Jingzhi Wu ◽  
Min Qiao ◽  
Zhifeng Lyu ◽  
Qianping Ran
Keyword(s):  
Reaction Time ◽  
Raw Materials ◽  
Reducing Agent ◽  
Optimal Conditions ◽  
Catalyst Amount ◽  
Dextrose Equivalent ◽  
Ft Ir ◽  
Dispersion Capacity ◽  
Anchoring Groups ◽  
And Performance

Using maltodextrin (MD) of different dextrose equivalent (DE) values, 1,3-propanesultone, and maleic anhydride as raw materials, a novel binary modified maltodextrin (BMMD) was synthesized and further applied as a water-reducing agent. Its structure was characterized by Fourier transform infrared (FT-IR) and UV. The rheological behavior of the sample solution and strengths for concrete were also determined and the adsorption was tested by TOC. The influence of the process parameters to degree of substitution (DS) and the dosage on the fluidity of cement paste were investigated. The results show that the optimal conditions of sulfonation were the MD of DE 15, m (sulfonated agent)/m (MD) of 1.4, the catalyst amount of 1% by mass MD, and the reaction time of 12 h; the optimal conditions of esterification were m (esterified agent)/m (SMD) of 0.6, the reaction temperature of 90°C, and the reaction time of 4 h. The optimal dosages of sulfonated maltodextrin (SMD) and BMMD were 0.475% and 0.45%, respectively. In this dosage, the main dispersion capacity of BMMD attributes to two kinds of anchoring groups (SO3-  &  COO-) and the appropriate molecular weight of MD.

scholarly journals Investigating the Effect of CuO/NiO and CuO/CoO Relative Composition on the Reduction Time of (CuO)x-(NiO)(1-x) and (CuO)x-(Co3O4)(1-x) with Methane Gas as the Reducing Agent in the Synthesis of Nano-bimetallic Nix-Cu(1-x) and Cux-Co(1-x)

2019 ◽  
Author(s):  
Hassan Ghanbarabadi ◽  
Behnam Khoshandam
Keyword(s):  
Reaction Time ◽  
Binary Mixtures ◽  
Raw Materials ◽  
Xrd Analysis ◽  
Reduction Reaction ◽  
Reducing Agent ◽  
Cobalt Oxides ◽  
Methane Gas ◽  
Copper Nickel ◽  
Relative Composition

In this paper, the reduction duration of (CuO)x-(NiO)(1-x) and (CuO)x-(Co3O4)(1-x) binary mixtures was studied using thermogravimetric method. The reduction reaction was performed using copper, nickel and cobalt oxides as metal precursors and methane gas as the reducing agent, under atmospheric pressure. The products as well as the raw materials were characterized and analyzed using X-Ray diffraction (XRD) and Energy Dispersive Spectroscopy (EDS). Initially, CoO, NiO and CuO were transformed to Co, Ni and Cu through reduction reactions with 23 Vol.% of methane at 830 °C. Results demonstrated that the reduction times of NiO, CoO and CuO NPs with CH4 at 830 °C were 14, 39 and 47 min, respectively. EDS and XRD analysis indicated that more than 97 % of copper, nickel and cobalt oxides were transformed to copper, nickel and cobalt NPs. The reaction time of (CuO)x-(NiO)(1-x) and (CuO)x-(Co3O4)(1-x) binary mixtures with methane was investigated to evaluate the effect of CuO (x=0, 0.4, 0.6, 1) relative composition. In addition, the reaction time of ternary mixture of (NiO)0.6-(CuO)0.2-(Co3O4)0.2 with methane gas was also studied.

Synthetic Technology and Performance of a Novel Fatty Alcohol Polyoxyethylene Carboxylate Surfactants

2011 ◽  
Vol 298 ◽  
pp. 163-168 ◽  
Author(s):  
Yuan Yuan Lei ◽  
Guo Zheng ◽  
Yu Sun ◽  
Yong Zhou
Keyword(s):  
Reaction Time ◽  
Optimum Condition ◽  
Sodium Hydroxide ◽  
Fatty Alcohol ◽  
Succinic Anhydride ◽  
Foam Stability ◽  
Raw Materials ◽  
Molar Ratio ◽  
New Type ◽  
And Performance

In this paper, with fatty alcohol polyoxyethylene (AEO9), succinic anhydride (SA) and sodium hydroxide as raw materials, a new type of fatty alcohol polyoxyethylene carboxylate surfactants (SAE9C-Na) was obtained by esterification and neutralizing effect. The influencing factors were researched and its surface properties were studied. The optimum condition of synthesis was determined: molar ratio of alcohol to acid was 1:1.1, reaction temperature was 85°C, reaction time was 60 min, under this condition, the yield could reach up to 95.8%. The results received from this experiment showed that SAE9C-Na had excellent surface activity and foaming and foam stability, whose emulsification and solubility enhancement were improved greatly.

scholarly journals Application of Box-Behnken Design in Optimization of Glucose Production from Oil Palm Empty Fruit Bunch Cellulose

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Satriani Aga Pasma ◽  
Rusli Daik ◽  
Mohamad Yusof Maskat ◽  
Osman Hassan
Keyword(s):  
Reaction Time ◽  
Oil Palm ◽  
Raw Materials ◽  
Glucose Production ◽  
Polynomial Equation ◽  
Empty Fruit Bunch ◽  
Optimal Conditions ◽  
Box Behnken Design ◽  
Order Polynomial ◽  
Validation Experiments

Oil palm empty fruit bunch fiber (OPEFB) is a lignocellulosic waste from palm oil mills. It contains mainly cellulose from which glucose can be derived to serve as raw materials for valuable chemicals such as succinic acid. A three-level Box-Behnken design combined with the canonical and ridge analysis was employed to optimize the process parameters for glucose production from OPEFB cellulose using enzymatic hydrolysis. Organosolv pretreatment was used to extract cellulose from OPEFB using ethanol and water as the solvents. The extracted cellulose was characterized by thermogravimetric analysis, FTIR spectroscopy, and field emission scanning electron microscopy. Hydrolysis parameters including amount of enzyme, amount of cellulose, and reaction time were investigated. The experimental results were fitted with a second-order polynomial equation by a multiple regression analysis and found that more than 97% of the variations could be predicted by the models. Using the ridge analysis, the optimal conditions reaction time found for the production of glucose was 76 hours and 30 min, whereas the optimum amount of enzyme and cellulose was 0.5 mL and 0.9 g, respectively. Under these optimal conditions, the corresponding response value predicted for glucose concentration was 169.34 g/L, which was confirmed by validation experiments.

Synthesis and Characterization of Zn-Ca-Mg-Al Hydrotacite-Like Compounds and its Application in the PVC

2011 ◽  
Vol 66-68 ◽  
pp. 65-69
Author(s):  
Long Feng Li ◽  
Yuan Gao ◽  
Mao Lin Zhang
Keyword(s):  
Reaction Time ◽  
Ph Value ◽  
Raw Materials ◽  
Treatment Temperature ◽  
Molar Ratio ◽  
Medium Ph ◽  
X Ray ◽  
Ft Ir ◽  
Thermal Stability Of

Ca-Mg-Al hydrotalcite-like compounds (CaMgAl-HTLcs) were synthesized by a hydrothermal method, and characterized by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and differential thermal analysis (DTA) techniques. The effects of the medium pH value, the molar ratio of the raw materials, the reaction temperature and the reaction time on the structure of CaMgAl-HTLcs were studied. The results showed that increasing treatment temperature and reaction time could improve the crystallinity and monodispersity of hydrotalcite-like compound particles. And well-defined CaMgAl-HTLcs could be prepared at a pH value of 10~11 with n(Zn+Mg+Ca):n(Al) =2. The products synthesized were applied to PVC to improve the thermal stability of PVC.

scholarly journals Chemical and Structural Characterization of Poplar and Black Pine Wood Exposed to Short Thermal Modification

2021 ◽  
Vol 72 (2) ◽  
pp. 155-167
Author(s):  
Vasiliki Kamperidou
Keyword(s):  
Raw Materials ◽  
Solid Wood ◽  
Thermal Modification ◽  
Moisture Loss ◽  
Black Pine ◽  
Pine Wood ◽  
Application Range ◽  
Ft Ir ◽  
And Performance ◽  
Wood Based Composite

In this study, poplar and black pine wood was exposed to short thermal treatments, aiming to improve some crucial properties. Using wet chemical analyses and Fourier-transform infrared spectroscopy (FT-IR), the influence of these treatments on the chemical composition of the modified species was investigated, as well as on the wood structure, using scanning electron microscopy. With the increase of heat treatment intensity, a mass loss of both species was recorded, attributed to the moisture loss and degradation of volatile compounds, as well as thermally less stable components. In the first treatment stages, the extractives presented a decrease, whereas with the duration and temperature increase, new extractives were formed. Lignin increased its network through ramification, especially at 200 ºC, while holocellulose was found lower in all modified wood categories of both species than in unmodified wood due to the intense decomposition of hemicelluloses. The findings of FT-IR analyses were in line with the chemical analysis results. The thermal modification process made wood materials more hydrophobic and dimensionally stable, providing protection against decomposing factors. At the same time, they were not intensively thermo-degraded, which increased their utilization perspectives and application range as solid wood of enhanced properties, or as wood particles/fibers participating as raw materials in wood-based composite products, wood-polymers composites etc., enhancing their materials compatibility, properties and performance.

Application of Response Surface Methodology for Improving the Yield of 1,5-bis(ptoluenesulfonyl)- 3,7-Dihydroxyoctahydro-1,5-Diazocine

2019 ◽  
Vol 16 (3) ◽  
pp. 398-404 ◽  
Author(s):  
Yang Zou ◽  
Jingyi Fei ◽  
Liangzhe Chen ◽  
Qingfeng Dong ◽  
Houbin Li
Keyword(s):  
Response Surface Methodology ◽  
Response Surface ◽  
Raw Materials ◽  
Low Cost ◽  
Product Yield ◽  
Synthesis Process ◽  
Optimal Conditions ◽  
Experimental Conditions ◽  
Simple Method ◽  
Ft Ir

Background: 3,3,7,7-tetrakis (difluoramino) octahydro-1,5-dinitro-1,5-diazocine (HNFX), as an important oxidizer in propellants, has received much attention due to its high density and energy. However, there are many difficulties that need to be solved, such as complex synthetic processes, low product yield, high cost of raw materials and complicated purification. In the synthesis of HNFX, the intermediate named 1,5-bis (p-toluenesulfonyl)-3,7-dihydroxyoctahydro-1, 5-diazocine (gem-diol), is difficult to synthesize. Methods: A simple method was used to synthesize the gem-diol. This prepared gem-diol was characterized by FT-IR, 1H NMR, melting point and mass spectrometry. In order to increase the yield of gem-diol, response surface methodology (RSM) was introduced to optimize experimental conditions. Results: After the establishment of the model, the optimal conditions of synthesis were found to be 9.33h for reaction time, 6.13wt. % for the concentration of NaOH and 1.38:1 for ratio of ECH (p-toluenesulfonamide): TCA (epichlorohydrin). Under the optimal conditions, the experimental value and the predicted value of yield were 22.18% and 22.92%, respectively. Conclusion: 1,5-bis (p-toluenesulfonyl)-3,7-dihydroxyoctahydro-1,5-diazocine (gem-diol) can be synthesized using the low cost of chemical materials, including p-toluenesulfonamide, epichlorohydrin, sodium hydroxide and ethanol. Response surface methodology (RSM) is an effective method to optimize the synthesis process, thereby improving the yield of gem-diol.

Preparation and Characterization of Formaldehyde Crosslinked Chitosan

2011 ◽  
Vol 239-242 ◽  
pp. 279-282 ◽  
Author(s):  
Juan Qin Xue ◽  
Jing Xian Li ◽  
Ming Wu ◽  
Wei Wang ◽  
Dong Ni Ma
Keyword(s):  
Reaction Time ◽  
Raw Materials ◽  
Cross Linking ◽  
Crosslinking Reaction ◽  
Optimal Conditions ◽  
Experimental Conditions ◽  
Crosslinked Chitosan ◽  
Chitosan Resin ◽  
Morphology Changes

Using formaldehyde as a crosslinking reagena novel cross-linked chitosan resin was synthesized by orthogonal. The resin material with good properties of sphericity and acidresistivity can be prepared under the optimal experimental conditions, which are found to be 1:6 for the ratio of chitosan and formaldehyde, 60°C for the temperature, 1 h for the reaction time, 640r/min for the stirring rate and 9 for the pH, and the cross-linking rate under the optimal conditions is 401.86%. SEM shows the surface morphology changes of raw materials and products; IR of the raw materials and products shows that the reaction occurs mainly on the amino and the hydroxyl of chitosan, and TG shows that the crosslinking reaction of chitosan can change its heat resistance.

Conversion of Glucose to Levulinic Acid Catalyzed by ZSM-5 Loading SO42-/ ZrO2

2013 ◽  
Vol 291-294 ◽  
pp. 249-252
Author(s):  
Ying Liu ◽  
Lu Lin ◽  
Xiao Yu Sui ◽  
Jun Ping Zhuang ◽  
Chun Sheng Pang
Keyword(s):  
Reaction Time ◽  
Reaction Temperature ◽  
Levulinic Acid ◽  
Temperature Reaction ◽  
Catalyst Amount ◽  
Hydroxymethyl Furfural ◽  
Ft Ir ◽  
Acid Catalyzed ◽  
Molar Percent ◽  
Hydrolysis Of

Hydrolysis of glucose to produce levulinic acid catalyzed by ZSM-5 loading SO42-/ ZrO2 was studied in this paper. The effects of different factors such as catalyst amount, reaction temperature, reaction time on the yields of levulinic acid and hydroxymethyl furfural were investigated. It was found that the highest yield of levulinic acid was 55.03% (molar percent) under the conditions of catalyst amount 3 g, reaction temperature 180 °C and reaction time 2.5 h. Surface structure of catalyst was analyzed by FT-IR, indicating that crystallinity of catalyst was 0.66.

Preparation and Characterization of Magnesium Borate Whisker

2013 ◽  
Vol 662 ◽  
pp. 481-484
Author(s):  
Zhi Liang Jin ◽  
Xu Jing ◽  
Yuan Hong ◽  
Xue Ying Nai ◽  
Li Wu
Keyword(s):  
Reaction Time ◽  
Molten Salt ◽  
Reaction Temperature ◽  
High Performance ◽  
Raw Materials ◽  
Price Ratio ◽  
Magnesium Borate ◽  
Synthesis Conditions ◽  
Ft Ir

Being a new whisker products with high performance to price ratio, magnesium borate whiskers with a length of 10 - 50μm and a diameter of 0.5 - 2μm were prepared by molten salt and characterized by XRD, FT - IR, SEM and chemical titration. The experiments show that the synthesis conditions are as follows: raw materials ratio: Mg:B:flux =1:11.05:1-3.5(mol); reaction temperature: 800 - 950°C;reaction time:6 - 10hours; flux: NaCl、KCl or NaOH.

Removal of Thiophene from Simulated Oil by Catalytic Oxidation Using K2FeO4/ V2O5

2011 ◽  
Vol 183-185 ◽  
pp. 1568-1572
Author(s):  
Yan Xiu Liu ◽  
Hua Song
Keyword(s):  
Reaction Time ◽  
Catalytic Oxidation ◽  
Sulfur Content ◽  
Reaction Temperature ◽  
Temperature Reaction ◽  
Optimal Conditions ◽  
Catalyst Amount ◽  
Deep Desulfurization

Oxidation extraction of thiophene from simulated oil by using K2FeO4as oxidant and methanol as extractant has been investigated. The effects of different catalyst, oxidant amount, catalyst amount, reaction temperature, reaction time, and extraction conditions were studied. This process is capable of decreasing the sulfur content of simulated oil from 100 mg•L-1to 17.8 mg•L-1at the optimal conditions. The results indicate that such a process could be an alternative to common hydrodesulfurization for deep desulfurization.

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