Water resistance evaluation of a MFU resins with different molar ratio catalyzed with citric acid

Author(s):  
J. Santos ◽  
J. Pereira ◽  
N. Paiva ◽  
J. Ferra ◽  
F.D. Magalhães ◽  
...  
1997 ◽  
Vol 3 (3) ◽  
pp. 196-202 ◽  
Author(s):  
Alexander Kaplan ◽  
Svetlana Kaplan ◽  
Karen F. Marcoe ◽  
Lester R. Sauvage ◽  
William P. Hammond

The turbidimetric method of Bom is the current approach for assessing the aggregation behavior of platelets. It has been of modest practical value, due to difficulty in standardizing laboratory techniques for plasma preparation and inadequate quantification of the aggregation process. We report a new technique of sedimented platelet rich plasma (SPRP) preparation that reduces the irregularities caused by factors associated with procuring and preparing blood samples and permits a more flexible protocol for laboratory practice. We quantified results with a platelet aggregation score, which is calculated by multiplying the ratio of the height of the initial wave of aggregation to the maximum height of the aggregation pattern by the total area under the aggregation curve and by the ratio of the whole blood platelet count and the number of platelets in the sample. Comparative analysis of platelet aggregation scores (n = 95) obtained with both plasma preparation techniques using a paired t test demonstrated no statistical differences ( t = 1.368, p = 0.174). To demonstrate the application of this modified method to evaluation of antiplatelet agents, the effects of aspirin and aspirin combined with citric acid on platelet aggregation were studied in vitro. The antiaggregatory effect of aspirin combined with citric acid was dependent on the pH and on their molar ratio, and was greater than the effect of aspirin alone. The SPRP protocol with platelet aggregation scoring methodology could be a valid alternative for measurement of the platelets' propensity to aggregate and the effect of antithrombotic treatments. Key Words: Platelet aggregation— Aspirin—Citric acid.


Author(s):  
Jilei Chao ◽  
Ruizhi Shi ◽  
Fuqiang Chu ◽  
Yanling Guo ◽  
Qian Deng

A kind of waterborne varnish for inkjet printing was synthesized, and properties of the waterborne varnish were characterized to make it suitable for the glazing requirements of inkjet printing and other printability requirements. The waterborne varnish was synthesized from epoxy resin (E-51), epoxy diluent (ED), acrylic acid, trimellitic anhydride, maleic anhydride and organic amine by three steps of ring opening reaction, esterification reaction, neutralization reaction. The viscosity, film-forming property, water absorption of waterborne varnish and the water resistance, lightness, wear resistance and bonding strength of coated paper were tested. The effects of the ratio of E-51 and ED in the polymerization system on the properties of waterborne varnish were studied. In the test of printability of self-made waterborne varnish, the absorption of digital inkjet paper to varnish and the influence of varnish on color reproduction of printed image were discussed and studied. The results show that when the molar ratio of epoxy group in E-51 and ED is about 1:1, the prepared varnish is suitable for inkjet printing, and its film-forming property, such as water resistance, adhesion and friction resistance are better. At the same time, its printability is also better.


2014 ◽  
Vol 900 ◽  
pp. 361-364
Author(s):  
Xiao Hui Wang ◽  
Xi Hua Du ◽  
Li Min Dong

Esters of Citric acid and palmityl alcohol were synthesized by esterification reaction under catalysis of cation exchange resin and P-toluene sulfonic acid respectively. The effects of amount of catalyst, ratio of raw materials, reaction time and temperature on the synthesis reaction were investigated . The experimental results showed that optimum of process conditions were 1:1~1:1.5 molar ratio of citric acid and palmityl alcohol, reaction temperature of 130~140°C, reaction time of 2 h. Conversion of palmityl alcohol were all more than 90% under 0.3% dosage using p-toluene sulfonic acid as the catalyst, or 0.5% dosage using 721 cation exchange resin with sulfonic acid type as catalyst. The synthesized product had good surface activity.


Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1995 ◽  
Author(s):  
Zhigang Wu ◽  
Bengang Zhang ◽  
Xiaojian Zhou ◽  
Lifen Li ◽  
Liping Yu ◽  
...  

Soybean protein hydrolysate, melamine, urea, and concentrated formaldehyde were used to synthesize an environmentally friendly soybean protein-melamine-urea-formaldehyde (SMUF) co-condensation resin. (NH4)2SO4, (NH4)2HPO4, (NH4)2HPO4 + (NH4)2SO4, (NH4)2HPO4 + (NH4)2S2O8, and (NH4)2HPO4 + (NH4)2SO4 + (NH4)2S2O8 were employed as curing agents for SMUF resin. The curing and thermal behaviors of the SMUF resin were investigated using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The results revealed the following: (1) (NH4)2SO4 alone could not cure the SMUF resin completely; thus, the final shear strength accomplished plywood with the resin was low, and its water resistance was poor, while the adhesive section was loose and porous/brittle after curing. (2) (NH4)2HPO4 could be hydrolyzed to generate H+ and promote SMUF curing, but it could also form polyphosphoric acids, resulting in crosslinking reactions with SMUF in parallel; thereby, the curing properties were improved. (3) When (NH4)2HPO4 + (NH4)2SO4 + (NH4)2S2O8 were engaged collectively as curing agent, the shear strength, water resistance, and heat resistance of SMUF attained were the best possible whereas the curing temperature was decreased and the heat released by curing was elevated substantially, which signifies maximized extent of crosslinking was achieved. Further, the adhesive section exhibited mostly a crosslinking intertexture as demonstrated by means of SEM. Accordingly, this study may serve as a guide for the curing of amino resins, with low-molar ratio of formaldehyde to amine in adhesives, which are applied to plywood production.


2015 ◽  
Vol 65 (5) ◽  
pp. 418
Author(s):  
Rekha Mann ◽  
Kiranmala Laishram ◽  
Sheikh Ashfaq Ahmed ◽  
Khavangkhui Zimik ◽  
Neelam Malhan

<p>Citrate nitrate sol freeze dry synthesis of 2 atomic % neodymium ion doped Yttrium Aluminium Oxide (Nd:YAG) nanopowders was explored for the first time. Sol was prepared by dissolving nitrates of Al3+, Y3+ and Nd3+ keeping molar ratio to be 5: 2.94: 0.06. Total metal ion to citric acid ratio was optimised at 1 is to 0.25. Sol was freeze dried at -80 °C for 48 h. Dried mass thus obtained was calcined at 1000 °C for 2 h to give phase pure Nd:YAG as characterised by FTIR and XRD. Particles were in the size range of 35 nm - 50 nm with close to spherical morphology as observed by TEM. Nanopowder was compacted and sintered at 1700 °C for 5 h under 10-6 mbar followed by hot isostatic press at 1750 °C for 4 h under 200 MPa, to give 71 per cent transmission at 1064 nm indicating synthesis of well sinterable Nd:YAG nanopowders.</p>


2015 ◽  
Vol 1107 ◽  
pp. 261-266
Author(s):  
Kean Pah Lim ◽  
Kuen Hou Cheong ◽  
Abdul Halim Shaari ◽  
Mansor Hashim ◽  
Albert Han Ming Gan ◽  
...  

In this paper, nanosized La0.85Na0.15MnO3 (LNMO) has been synthesized via sol-gel method by involving two major steps, first the complexation of citric acid (CA) with metal ions (MI) and second the polyesterification between CA and ethylene glycol (EG). The effect of molar ratio CA:MI varying from 2-4 on structure, microstructure and electrical transport properties of LNMO have been investigated by constant the amount of EG. All samples show single perovskite phase with hexagonal structure and space group R3c after sintering at 800°C for 10h. Sample of molar ratio 2.5 is observed to possess smallest grain sizes which yield high resistivity value compared with others, is suggested to originate from the increase of tunneling barriers (grain boundaries). The large low field magnetoresistance (LFMR) of about ~ -16% at 0.1T and low temperature confirmed the important role of grain boundaries in the nanosized LNMO.


Membranes ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 607
Author(s):  
Muthia Elma ◽  
Anna Sumardi ◽  
Adhe Paramita ◽  
Aulia Rahma ◽  
Aptar Eka Lestari ◽  
...  

The physicochemical properties of organo-silica xerogels derived from organo catalyst were pervasively investigated, including the effect of one-step catalyst (citric acid) and two-step catalyst (acid-base), and also to observe the effect of sol pH of organo-silica xerogel toward the structure and deconvolution characteristic. The organo-silica xerogels were characterized by FTIR, TGA and nitrogen sorption to obtain the physicochemical properties. The silica sol–gel method was applied to processed materials by employing TEOS (tetraethyl orthosilicate) as the main precursor. The final molar ratio of organo-silica was 1:38:x:y:5 (TEOS:ethanol: citric acid: NH3:H2O) where x is citric acid concentration (0.1–10 × 10−2 M) and y is ammonia concentration (0 to 3 × 10−3 M). FTIR spectra shows that the one-step catalyst xerogel using citric acid was handing over the higher Si-O-Si concentration as well as Si-C bonding than the dual catalyst xerogels with the presence of a base catalyst. The results exhibited that the highest relative area ratio of silanol/siloxane were 0.2972 and 0.1262 for organo catalyst loading at pH 6 and 6.5 of organo-silica sols, respectively. On the other hand, the organo-silica matrices in this work showed high surface area 546 m2 g−1 pH 6.5 (0.07 × 10−2 N citric acid) with pore size ~2.9 nm. It is concluded that the xerogels have mesoporous structures, which are effective for further application to separate NaCl in water desalination.


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