Study on the Synthesis Optimization of Paper Wet-Strengthening Resin PAE

2011 ◽  
Vol 236-238 ◽  
pp. 1135-1138
Author(s):  
Shi Min Chen ◽  
Hong Xiang Zhu ◽  
Nan Nan Xia ◽  
Shuang Fei Wang ◽  
Hai Nong Song

The Polyamide Polyamine Epichlorhydrin Resin was obtained by using adipic acid, diethylene triamine and epoxy chloropropane as raw materials. The factors that would affect the properties of PAE resin were considered, including the reaction time, the dosage of the epoxy chloropropane, the injection time of epoxy chloropropane and the soaking time, and the wet strengthening property of PAE resin were studied through experiments. The results are as following: the ratio of epoxy chloropropane to diethylenetriamine is 1:1, the injection time of epoxy chloropropane is 8.5 min, the reaction temperature is 75 °C and the soaking time is 35min~40min. Under the optimum conditions, the PAE has a higher wet-strength and solid content, and its viscosity up to 25~35cp.

2012 ◽  
Vol 557-559 ◽  
pp. 1070-1073 ◽  
Author(s):  
Qian Qian Xing ◽  
Chuan Shan Zhao ◽  
Wen Jia Han

PAE as the wet strength agent has a long history; it not only has the wet strength performance and the retention and drainage characteristics. This paper focuses on the technological conditions of preparation of PAE wet-strength agent and the application conditions. The results showed that the well PPC was obtained under the following conditions: the mole ratio of adipic acid and diethylenetriamine were 1:1.05, the amount of catalyst (mole ratio of the total raw materials) was 1%, the temperature of heat preservation was 165°C and the reaction time was 4h. The optimum condition of preparing PAE was obtained as followings: the ratio of EPI to PPC of 1.2:1, the epoxidation temperature of 60°C and reaction time of 2h. While applied in softwood pulp, when the dosage of PAE was 1%, the wet strength agent provided the satisfactory effect.


2009 ◽  
Vol 6 (1) ◽  
pp. 189-195 ◽  
Author(s):  
Xiu-Yan Pang ◽  
Ting-Ting You

Biodiesel was obtained through transesterification of animal oil and ethanol under the catalysis of SO42-/ TiO2We have inspected the activation of SO42-/ TiO2prepared under different dipping vitriol concentration,baking activation temperature. The optimum conditions to prepare SO42-/ TiO2are; dipping vitriol concentration of TiCl4 hydrolysis product is 1.5 mol / L, baking activation temperature for this catalyst takes 500°C. It can guarantee the catalyst has a smaller size and a higher load of vitriol. With animal oil as raw materials, ethanol as transesterifying agent and SO42-/ TiO2as catalyst, the influence of reaction time, mass ratio of ethanol to oil and the dosage of catalyst were investigated. Optimum condition to obtain biodiesel was studied through orthogonal experiment, and it is listed as follow: mass ratio of ethanol to oil is 1.5:1.0, dosage of catalyst is 30 g SO42-/ TiO2versusper 100 g animal oil, and reaction time is 8.0 h when reaction temperature is controlled as 80°C. The yield of biodiesel is 0.796 g/g under the above condition. SO42-/ TiO2can be used as an effective catalyst during transesterification of animal oil and ethanol, and it can be reused


2014 ◽  
Vol 692 ◽  
pp. 326-331
Author(s):  
Fang Peng ◽  
Hui Zhao ◽  
Shui Jin Yang

A new environmental friendly catalyst, H4SiW6Mo6O40/TiO2-SiO2 was prepared by impregnation method, the synthesis of cyclohexanone 1,2-propanediol ketal was the probe reaction to optimize the synthetic condition of catalyst. The reactive condition of catalyst was optimized by orthogonal test method. The optimum conditions are n (TiO2): n (SiO2)= 3: 1, 20 % mass ratio of m (H4SiW6Mo6O40): m (TiO2-SiO2), the calcined time is 3 h and 300 °C of activated temperature. Using H4SiW6Mo6O40/TiO2-SiO2 as catalyst, adipic acid was synthesized from the oxidation of cyclohexanone by 30 % H2O2. Influences of dosage of H4SiW6Mo6O40/TiO2-SiO2, reaction temperature, volume of hydrogen peroxide and reaction time were discussed. Experimental results showed that H4SiW6Mo6O40/TiO2-SiO2 is a good catalyst for synthesis of adipic acid. When n (cyclohexene): n (H2O2): n (H4SiW6Mo6O40/TiO2-SiO2)= 100: 979: 0.04, reaction temperature is 130 °C and reaction time is 5 h, under the optimum conditions, the yield of adipic acid is 45.9 %.


2018 ◽  
Vol 8 (1) ◽  
pp. 121-127 ◽  
Author(s):  
Tanzer Eryilmaz

In this study, the methyl ester production process from neutralized waste cooking oils is optimized by using alkali-catalyzed (KOH) single-phase reaction. The optimization process is performed depending on the parameters, such as catalyst concentration, methanol/oil ratio, reaction temperature and reaction time. The optimum methyl ester conversion efficiency was 90.1% at the optimum conditions of 0.7 wt% of potassium hydroxide, 25 wt% methanol/oil ratio, 90 min reaction time and 60°C reaction temperature. After the fuel characteristics of the methyl ester obtained under optimum conditions were determined, the effect on engine performance, CO and NOx emissions of methyl ester was investigated in a diesel engine with a single cylinder and direct injection. When compared to diesel fuel, engine power and torque decreased when using methyl ester, and specific fuel consumption increased. NOx emission increases at a rate of 18.4% on average through use of methyl ester.


2012 ◽  
Vol 83 (4) ◽  
pp. 381-395 ◽  
Author(s):  
Longfang Ren ◽  
Guohui Zhao ◽  
Taotao Qiang ◽  
Xuechuan Wang ◽  
Na Wang

In the current study, amino-terminated hyperbranched polymers (NH2-HBP) were synthesized by Michael addition reaction in which N, N’-methylene bisacrylamide (MBA) and diethylene triamine (DETA) were used as raw materials, and water was used as a solvent. Reaction temperature, raw material ratio, and reaction time were optimized via single-factor experiments in which the production rate and primary amino content were used as indexes. The results showed that the mol ratio of MBA to DETA was 1:1.1, the temperature was 70°C, and reaction time was 24 h. Under this condition, the primary amino content of NH2-HBP was 2.83 mmol/g, and the yield was 91.16%. The NH2-HBP structure was characterized by Fourier transform infrared spectroscopy and nuclear magnetic resonance. Moreover, the relative molecular mass distribution of NH2-HBP was also determined by gel permeation chromatography. As an active substance, NH2-HBP was grafted onto the polyamide microfiber synthetic leather used in clothes, and organic phosphine was used as a cross-linking agent. The change in dye uptake, surface chroma, and resistance to dry-rub and wet-rub fastness properties was discussed. When the NH2-HBP dosage was 5.5%, the dye uptake improved from 56.89% to 94.85% (an increase of almost 61%). The surface chroma also deepened, the dry-rub fastness improved from 3.0 to 4.5, and the wet-rub fastness improved from 2.5 to 3.5.


2011 ◽  
Vol 393-395 ◽  
pp. 1413-1416
Author(s):  
Yu Xiang Wang ◽  
Dan Dan Li ◽  
Xing Huang ◽  
Ya Juan Zhao

The selective hydrogenation of 4,4'-methylenedianiline(MDA) over Ru/γ-Al2O3 was investigated in the presence of diamine and base. Under the optimum conditions: the reaction temperature of 448K, H2 pressure of 1100 psig , and reaction time of 5h, the conversion of 4,4'-methylenedianiline was close to 100% and the selectivity to trans-trans isomer of 4,4'-diamino-dicyclohexy was less than 20%.


2013 ◽  
Vol 781-784 ◽  
pp. 276-279
Author(s):  
Yu Hang Zhao ◽  
Li Cui ◽  
Da Zhi Wang ◽  
Tong Kuan Xu ◽  
Yong Peng Li

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%.


2017 ◽  
Vol 45 ◽  
pp. 34-41 ◽  
Author(s):  
Qin Shi ◽  
Jing Xu ◽  
Li Feng Dang ◽  
Jun Chen ◽  
Guo Gang Tang ◽  
...  

TiSe2 nanobelts/nanoplates have been successfully fabricated through a facile and environment-friendly pressureless sintered process using micro-sized Ti and Se elements as raw materials. The morphology and structure of the as-prepared TiSe2 products were investigated by X-ray diffractometer, scanning electron microscopy, transmission electron microscopy and high resolution transmission electron microscopy. The experimental results indicated that the morphology of TiSe2 products were strongly dependent on the reaction temperature and reaction time. As the reaction temperature was set at 600°C and 800°C, long belts-like and plates-like structures of as-prepared TiSe2 products could be observed, respectively. However, a mixture of nanobelts and nanoplates could be obtained at a reaction temperature of 700°C. It was also found that the reaction time played a crucial role in obtaining the homogeneous distribution nanoparticles, therefore, reasonable reaction process and formation mechanisms of as-prepared TiSe2 nanoparticles were proposed. Moreover, the tribological properties of the TiSe2 nanobelts/nanoplates were investigated. The test results showed that the addition of TiSe2 nanoparticles could improve the tribological properties of base oil. Furthermore, the friction coefficient of base oil containing TiSe2 nanoplates was lower and more stable than those of TiSe2 nanobelts and pure base oil.


2012 ◽  
Vol 602-604 ◽  
pp. 739-742
Author(s):  
Rui Xia Niu ◽  
Bo Lin Li ◽  
Biao Long

Poly(bis(2-(trimethylamino)ethyl) 2-hydroxyl propylidene ammonium) chloride (PTMAEPAC) is one kind of oligomeric cationic polymer with a quarter nitrogen atom on its main and side chain. It was synthesized from Bis(2-trimethyl ammonium)ethyl ammonium chloride (TMAEAC) and epichlorohydrin (ECH) by copolymerization reaction, effects of reaction temperature, mole ratio of raw materials, reaction time, amount of solvent on the cationicity of product were studied. The structure of PTMAEPAC was confirmed by IR and 1H-NMR, and its anti-clay-expanding ability was studied. The results show that the cationicity of PTMAEPAC can reach 83.9% with the reaction time of 6h at 65°C when TMAEAC-to-ECH mole ratio is 1.2:1 and the amount of solvent is 30% in total. According to the IR and NMR analysis the product has the same structure with the aim compound. When the content of the product is 3 wt% it has a good anti-clay-expanding ratio of 96.1%.


2011 ◽  
Vol 347-353 ◽  
pp. 3873-3876
Author(s):  
Adama Yousif ◽  
Xu Zeng ◽  
Fang Ming Jin ◽  
Yan Fang

In this paper, an efficient method for producing lactic acid from glucose with nickel as a catalyst under hydrothermal conditions has been developed. The addition of nickel can improve the lactic acid yield efficiently under alkaline hydrothermal conditions. The highest lactic acid yield of 35% was obtained under the optimum conditions, i.e., reaction temperature 300 °C, reaction time 60 s, 0.5 mmol nickel and 2.5 M NaOH.


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