scholarly journals Investigation and Characterization of Synthesis Conditions on Sucrose-ammonium Dihydrogen Phosphate (SADP) Adhesive: Bond Performance and Chemical Transformation

Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4078 ◽  
Author(s):  
Shijing Sun ◽  
Min Zhang ◽  
Kenji Umemura ◽  
Zhongyuan Zhao
Keyword(s):  
Chemical Analysis ◽  
Chemical Transformation ◽  
Raw Material ◽  
Synthesis Process ◽  
Dihydrogen Phosphate ◽  
Ammonium Dihydrogen Phosphate ◽  
Synthesis Time ◽  
Synthesis Conditions ◽  
Renewable Chemicals ◽  
Bond Performance

Sucrose is one of the most abundantly available renewable chemicals in the world, and it is expected to be utilized as a raw material for wood-based material products. Herein, a novel adhesion system that was based on sucrose and ammonium dihydrogen phosphate (ADP) was synthesized into an adhesive with 80% solid content, and this eco-friendly was utilized on the fabrication of plywood. The effects of the synthesis conditions on the plywood bond performance and synthesis mechanism were investigated. The optimal synthesis conditions were as follows: the mass proportion between sucrose and ADP was 90/10, the synthesis temperature was 90 °C, and the synthesis time was 3 h. The bonding performance of the plywood that was bonded by optimal SADP adhesive satisfied the GB/T 9846-2015 standard. The chemical analysis was performance tested by using High-Performance Liquid Chromatography (HPLC), Attenuated Total Reflection-Fourier Transform Infrared Spectra (ATR-FTIR), and Pyrolysis Gas Chromatography and Mass Spectrometry (Py-GC/MS) to understand the chemical transformation during the synthesis process. The chemical analysis results confirmed that the hydrolysis and conversation reaction of sucrose occurred in the synthesized SADP adhesive, and ADP promoted the pyrolysis efficiency of sucrose.

scholarly journals Further Exploration of Sucrose-Citric Acid Adhesive: Synthesis and Application on Plywood

Polymers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1875 ◽  
Author(s):  
Shijing Sun ◽  
Zhongyuan Zhao ◽  
Kenji Umemura
Keyword(s):  
Citric Acid ◽  
Research Direction ◽  
Synthesis Temperature ◽  
Solid Content ◽  
National Standard ◽  
Synthesis Process ◽  
Synthesis Mechanism ◽  
Synthesis Time ◽  
Synthesis Conditions ◽  
Bond Performance

The development of eco-friendly adhesives is a major research direction in the wood-based material industry. Previous research has already demonstrated the mixture of sucrose and citric acid could be utilized as an adhesive for the manufacture of particleboard. Herein, based on the chemical characteristics of sucrose, a synthesized sucrose-citric acid (SC) adhesive was prepared, featuring suitable viscosity and high solid content. The investigation of synthesis conditions on the bond performance showed that the optimal mass proportion between sucrose and citric acid was 25/75, the synthesis temperature was 100 °C, and the synthesis time was 2 h. The wet shear strength of the plywood bonded with SC adhesive, which was synthesized at optimal conditions and satisfied the China National Standard GB/T 9846-2015. The synthesis mechanism was studied by both 13C NMR analysis and HPLC, and the chemical composition manifesting caramelization reaction occurred during the synthesis process. The results of ATR FT-IR indicated the formation of a furan ring, carbonyl, and ether groups in the cured insoluble matter of the SC adhesive, which indicated dehydration condensation as the reaction mechanism between sucrose and citric acid.

scholarly journals Synthesis of Molecularly Imprinted Polymer via Emulsion Polymerization for Application in Solanesol Separation

2020 ◽  
Vol 10 (8) ◽  
pp. 2868 ◽  
Author(s):  
Guojie Zhao ◽  
Jing Liu ◽  
Minghong Liu ◽  
Xiaobin Han ◽  
Yulong Peng ◽  
...  
Keyword(s):  
Emulsion Polymerization ◽  
Molecularly Imprinted Polymers ◽  
Current Method ◽  
Synthesis Process ◽  
Cross Linking ◽  
Adsorption Effect ◽  
Synthesis Time ◽  
Molecularly Imprinted ◽  
Imprinted Polymers ◽  
Synthesis Conditions

High-purity solanesol can be used for pharmaceutical applications, but the current method for purifying solanesol has high cost and difficult continuous operation, and the use of molecular imprinting to purify natural products is a hot research topic of current research. Solanesol molecularly imprinted polymers were synthesized via emulsion polymerization for the first time. The morphology of the SSO-MIPs was observed with a scanning electron microscope, and the effects of the synthesis time, initiator dosage, functional monomer dosage, and cross-linking agent dosage on the adsorption effects under high-temperature and rapid synthesis conditions were discussed. The results demonstrate that the optimum synthesis conditions were a ratio of the template molecules to the functional monomers to the cross-linking agents of 1:8:30 (mol:mol:mol), 10 mg of the initiator, and a synthesis temperature of 70 °C. The imprinting factor of SSO-MIPs synthesized under the optimized process was found to reach 2.51, and the SSO-MIPs synthesized by this method exhibited a good adsorption effect, emitted less pollution during the synthesis process, and are convenient for demulsification. This research reports a reliable method for the synthesis of solanesol molecularly imprinted polymers.

Influence of Composition and Isothermal Sintering on the Properties of Hydroxyapatite Bioceramic Bodies

2014 ◽  
Vol 979 ◽  
pp. 347-350
Author(s):  
Rungsarit Koonawoot ◽  
Cherdsak Saelee ◽  
Sakdiphon Thiensem ◽  
Sittiporn Punyanitya
Keyword(s):  
High Efficiency ◽  
Bending Strength ◽  
Strength Properties ◽  
Raw Material ◽  
Dihydrogen Phosphate ◽  
Ammonium Dihydrogen Phosphate ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

This work reports the influence of chemical composition and sintering schedule on the properties of sintered bodies of hydroxyapatite (HA) bioceramic. The method of preparing sintered bodies by solid state reaction and uniaxial pressing. The raw material used calcium carbonate (CaCO3) and ammonium dihydrogen phosphate (NH4H2PO4) powder as precursors. These powders were mixed at CaCO3: NH4H2PO4 mass ratio of 1:0.697, 1:0.692, 1:0.689, 1:0.685 and 1:0.68, respectively. The compositions in the temperatures range of 800-1300 °C for 3 hour. The sintered bodies were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and Fourier transform infrared spectroscopy (FTIR). Properties including phase, microstructures, porosity and bending strength of the samples. The results show that green bodies can be sintered at 1150 °C for 3 hours. This temperature found that crystals growth, highest of HA phase content in sintered bodies, good density and high efficiency strength properties.

scholarly journals Water-Preserving and Salt-Resistant Slow-Release Fertilizers of Polyacrylic Acid-Potassium Humate Coated Ammonium Dihydrogen Phosphate

Polymers ◽  
2021 ◽  
Vol 13 (17) ◽  
pp. 2844
Author(s):  
Hongping Li ◽  
Lanwen Yang ◽  
Jianxin Cao ◽  
Chenchen Nie ◽  
Hao Liu ◽  
...  
Keyword(s):  
Polyacrylic Acid ◽  
Slow Release ◽  
Salt Resistance ◽  
Deionized Water ◽  
Synthesis Process ◽  
Dihydrogen Phosphate ◽  
Water Absorbency ◽  
Ammonium Dihydrogen Phosphate ◽  
Potassium Humate ◽  
Salty Water

Polyacrylic acid (PAA) has high water absorbency but poor salt resistance. Humic acid (HA) extracted from lignite was introduced into the cross-linked copolymer systems of AA to improve the water absorbency and salt-tolerance. A polyacrylic acid-potassium humate (PAA-KHA) coated ammonium dihydrogen phosphate (ADP) fertilizer with water-preserving, salt-resistant and slow-release properties was prepared. The main properties of HA extracted from lignite oxidized by H2O2 were studied. Furthermore, the synthesis process, water absorbency of PAA-KHA in deionized water and in NaCl solution, morphologies of PAA-KHA, and the slow-release performance of the fertilizer (ADP@PAA-KHA) were investigated. The results showed PAA-KHA had a layered interpenetrating network, which can provide sufficient storage space for water and nutrients. The salty water absorbency of PAA-KHA increased by about 3 times compared to PAA. Both the PO43− and NH4+ cumulative release of ADP@PAA-KHA with a coating rate of 10% in deionized water, were less than 20% within 24 h, and were 55.71% and 28.04% after the 15th day, respectively. The weight change of ADP@PAA-KHA before and after absorbing water was about 53 times in deionized water and about 4 times in 1 wt% of NaCl salty water. The results show that ADP@PAA-KHA has excellent properties of water retention, salt resistance and slow-release. This will efficiently improve the utilization of fertilizer and reduce the irrigation water consumption at the same time.

Flash synthesis of zirconia nanoparticles by microwave forced hydrolysis

2001 ◽  
Vol 16 (9) ◽  
pp. 2619-2622 ◽  
Author(s):  
K. Bellon ◽  
D. Chaumont ◽  
D. Stuerga
Keyword(s):  
Microwave Heating ◽  
Correlation Spectroscopy ◽  
Synthesis Process ◽  
Heating Rates ◽  
Fast Heating ◽  
Synthesis Time ◽  
X Ray ◽  
Synthesis Conditions ◽  
Microwave Reactor ◽  
Forced Hydrolysis

Forced hydrolysis preparation of zirconia sols and powders by microwave heating of zirconium tetrachloride solutions at temperatures equal to 180 °C leads in a few minutes to monodispersed nanoscale zirconia particles. Synthesis was performed in a microwave reactor called the RAMO system. This microwave reactor was designed by the authors. This flash-synthesis process combines the advantages of forced hydrolysis (homogeneous precipitation) and microwave heating (very fast heating rates). The sols and powders were characterized by x-ray diffraction,photon correlation spectroscopy (PCS), small-angle x-ray scattering, and transmission electron microscopy. Sols are colloidally stable, which means that after 6 months no sedimentation is observed and the size distribution given by PCS measurements has not changed. For all synthesis conditions (with or without HCl, zirconium salt concentration, and synthesis time), zirconia polycrystalline particles were produced. According to the different analyses, these zirconia polycrystalline particles were constituted of aggregates of small primary clusters.

The Effect of Phosphatic Composite on Magnesium Phosphate Cement Performance

2014 ◽  
Vol 809-810 ◽  
pp. 477-484
Author(s):  
Zhao Qing Qi ◽  
Hong Tao Wang ◽  
Jun Liang Dang ◽  
Shi Hao Zhang ◽  
Jian Hua Ding
Keyword(s):  
Setting Time ◽  
Potassium Dihydrogen Phosphate ◽  
Magnesium Phosphate ◽  
Dihydrogen Phosphate ◽  
Ammonium Dihydrogen Phosphate ◽  
Hydrogen Phosphate ◽  
Sodium Dihydrogen Phosphate ◽  
Disodium Hydrogen Phosphate ◽  
Potassium Dihydrogen ◽  
Sodium Dihydrogen

The capacity of 10%, 30%, and 50% ammonium dihydrogen phosphate were replaced with an equal amount of three phosphate (potassium dihydrogen phosphate, sodium dihydrogen phosphate, disodium hydrogen phosphate) respectively. Magnesium phosphate cement was made by phosphate of replaced, which strength, setting time, fluidity, hydration temperature, and the hydration products was researched. The results show that: MPC was made that replaced with the equal amount of three kind of phosphate, which has good mechanical properties. Setting time and fluidity change along with the replacment. Three kind of phosphate replace ammonium dihydrogen phosphate, which change the hydration process of MPC. When ammonium dihydrogen phosphate was replaced by an equal amount of disodium hydrogen phosphate, the temperature of hydration is only 69.4 °C. XRD showed that the diffraction peaks of composite’s magnesium phosphate cement increases.

Growth and Characterization of Ammonium Dihydrogen Phosphate (ADP) Doped with H3BO3 Crystals Grown by Slow Evaporation Method

2016 ◽  
Vol 675-676 ◽  
pp. 573-576 ◽  
Author(s):  
Pratya Thongpanit ◽  
Weerapong Chewpraditkul ◽  
Nakarin Pattanaboonmee
Keyword(s):  
Boric Acid ◽  
Temperature Stability ◽  
Hardness Measurement ◽  
Dihydrogen Phosphate ◽  
Ammonium Dihydrogen Phosphate ◽  
Slow Evaporation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Evaporation Method

Ammonium dihydrogen phosphate (ADP) crystals is very interesting due to its nonlinear optical property. This study investigated on improving of material for academic use by adding boric acid to modify ADP crystals. Slow evaporation method in aqueous solutions of pure ADP and ADP doped with three concentrations of H3BO3 as 0.1, 1.0, 5.0 %wt were studied. The grown crystals were confirmed tetragonal structure by powder X-ray diffraction studies. The FTIR spectrum analysis presented various functional groups of boron in three conditions of doped ADP. TGA study was comfirned the temperature stability at 220 °C for both pure and doped ADP crytals. The machanical stress was analyzed by Vicker’s hardness measurement. The results of this analysis showed boric acid doped 1.0 %wt had superior machanical stress from 10 to 75 grams. ADP doped with boric acid at 1.0 %wt was accepted in all test properties.

Sign in / Sign up

Export Citation Format

Share Document