Preparation and Properties of Waterborne Varnish for On-Demand Inkjet Printing

2021 ◽  
Author(s):  
Jilei Chao ◽  
Ruizhi Shi ◽  
Fuqiang Chu ◽  
Yanling Guo ◽  
Qian Deng
Keyword(s):  
Inkjet Printing ◽  
Ring Opening ◽  
Water Resistance ◽  
Epoxy Group ◽  
Molar Ratio ◽  
Esterification Reaction ◽  
Trimellitic Anhydride ◽  
Friction Resistance ◽  
Ring Opening Reaction ◽  
Film Forming

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.

scholarly journals Radical-induced cationic frontal polymerisation for prepreg technology

2021 ◽  
Vol 152 (1) ◽  
pp. 151-165
Author(s):  
Anh Dung Tran ◽  
Thomas Koch ◽  
Robert Liska ◽  
Patrick Knaack
Keyword(s):  
Mechanical Properties ◽  
Ring Opening ◽  
Storage Stability ◽  
Epoxy Group ◽  
Epoxide Resin ◽  
Ring Opening Reaction ◽  
Thermal Mechanical Properties ◽  
Radical Polymerisation ◽  
New Type ◽  
Dual Curing

AbstractIn this study, a new type of prepreg technology has been established using a dual curing system consisting of 1,6-hexanediol diacrylate (HDDA) and frontally polymerisable components based on the epoxide resin. The study of the polymerisation of HDDA revealed (tert-butylcyclohexyl)peroxydicarbonate (BCPC) as the most suitable radical thermal initiator. The presence of BCPC resulted in a fast radical polymerisation of HDDA and no cationic ring-opening reaction of the epoxy, which was observed by monitoring the double bond and epoxy group conversion in real time-NIR rheology measurement. The formed prepreg can subsequently be cured by radical-induced cationic frontal polymerisation of the epoxy resin. Effects of HDDA amount on the radical polymerisation, stiffness of the gel, frontal parameters and thermal mechanical properties of final polymers were investigated. With 10 wt% HDDA, the formed prepreg has very good storage stability, which was proved by monitoring the epoxy group conversion during 4 months of storage at 50 °C while still a stable front can be obtained. Furthermore, the RICFP-prepregs with different fibre contents were prepared and polymerised by RICFP. Then, a snowflake composite was successfully produced using RICFP-prepreg. Graphic abstract

Preparation of Epoxy Modified Organosilicone High-Temperature Resistance Coatings

2008 ◽  
Vol 373-374 ◽  
pp. 434-437
Author(s):  
Hua Zhu ◽  
Zhi Lang Chen ◽  
Fang Nan ◽  
An Lin ◽  
Fu Xing Gan
Keyword(s):  
High Temperature ◽  
Epoxy Resin ◽  
Adhesion Strength ◽  
Ring Opening ◽  
Epoxy Group ◽  
Temperature Resistance ◽  
Ring Opening Reaction ◽  
High Temperature Resistance ◽  
Solidification Reaction ◽  
The Fourier Transform

An ambient-cured organosilicone resin modified with epoxy resin was synthesized with lab-synthesized polysiloxane resin and biphenix-A epoxy resin(E-20) by copolymerization at 180~190 °C for 2~3 hours. The effect of ratios between polysiloxane resin and E-20, reaction temperatures and reaction time on heat resistance and miscibility etc were discussed in detail. The experiment results showed that the epoxy modified organosilicone resin exhibited the best solubility performance and adhesion strength when the ratio of the polysiloxane resin to E-20 was 3:7. The Fourier transform infrared spectra (FTIR) revealed that hydroxy on epoxy resin had reacted with ethyoxyl on organic silicon molecular chain, but no ring-opening reaction happened on epoxy group of E-20. The excellent high-temperature resistance painting, based on these epoxy modified organosilicone resin was prepared with flake aluminum powder as temperature resistance filler, polyamide 650 as curer and WD-50 coupling agent as curing-promoter. It was shown that the temperature resistance was superior to 600°C and the adhesion strength of the coating was up to 1 grade. Scanning electron microscope(SEM) revealed the reaction happened on -Si-O-Si- and Al under high temperature improved the coatings to resist higher temperature. The mechanism of the high-temperature anticorrosion is attributed to “ring-opening reaction” and “cross-link solidification reaction”.

Synthesis and Characterization of Poly(Lactic Acid)-Grafted Natural Rubber by Reactive Melt-Blending Technique

2018 ◽  
Vol 382 ◽  
pp. 7-11
Author(s):  
Yodsathorn Wongngam ◽  
Cattaleeya Pattamaprom
Keyword(s):  
Lactic Acid ◽  
Natural Rubber ◽  
Ring Opening ◽  
Degree Of Polymerization ◽  
Hydroxyl Group ◽  
Synthesis And Characterization ◽  
Poly Lactic Acid ◽  
Esterification Reaction ◽  
Ring Opening Reaction

This study investigated the synthesis and characterization of poly(lactic acid)-grafted natural rubber (PLA-g-NR) in molten state. The grafting was carried out in an internal mixer without and with the presence of tin octoate catalyst (TO). The grafting of lactide onto NR was carried out by using maleic anhydride (MA) as a linker. The FTIR and 1H-NMR spectra revealed new peaks for the MA-grafted NR (NR-g-MA) and PLA indicating that MA was grafted onto NR and that LA was successfully polymerized into PLA. It was also found that MA grafted onto NR could assist as a linker for connecting PLA with NR via esterification reaction between hydroxyl group (OH) at the end chain of PLA and carboxylic group (COOH) from ring opening reaction of MA. Moreover, the decrease of residual LA peak in FTIR spectra suggested that the presence of TO catalyst in the reactive blend promoted higher degree of polymerization of PLA from ring opening reaction of LA.

On the Conrotatory Ring Opening of 3-Carbomethoxycyclobutene Vis-À-Vis 3-Carbomethoxy-1,2-Benzocyclobutene and the Predominant Inward Opening of 3-Dimethylaminocarbonyl-1,2-Benzocyclobutene

2018 ◽  
Author(s):  
Veejendra Yadav ◽  
Dasari L V K Prasad ◽  
Arpita Yadav ◽  
Maddali L N Rao
Keyword(s):  
Transition State ◽  
Ring Opening ◽  
Electron Process ◽  
Ring Opening Reaction ◽  
Stable Species ◽  
Electron Event

<p>The torquoselectivity of conrotatory ring opening of 3-carbomethoxycyclobutene is controlled by p<sub>C1C2</sub>→s*<sub>C3C4</sub> and s<sub>C3C4</sub>→p*<sub>CO</sub> interactions in the transition state in a 4-electron process as opposed to only s<sub>C3C4</sub>→p*<sub>CO</sub> interaction in an apparently 8-electron event in 3-carbomethoxy-1,2-benzocyclobutene. The ring opening of 3-carbomethoxy-1,2-benzocyclobutene is sufficiently endothermic. We therefore argue that the reverse ring closing reaction is faster than the forward ring opening reaction and, thus, it establishes an equilibrium between the two and subsequently allows formation of the more stable species <i>via</i> outward ring opening reaction. Application of this argument to 3-dimethylaminocarbonyl-1,2-benzocyclobutene explains the predominantly observed inward opening.</p>

scholarly journals Expanding Monomers as Anti-Shrinkage Additives

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 806
Author(s):  
Philipp Marx ◽  
Frank Wiesbrock
Keyword(s):  
Ring Opening ◽  
Covalent Bond ◽  
Volumetric Shrinkage ◽  
Structure Property ◽  
Atomic Packing ◽  
Materials Properties ◽  
Volumetric Expansion ◽  
Structure Property Relationships ◽  
Ring Opening Reaction ◽  
Measuring Techniques

Commonly, volumetric shrinkage occurs during polymerizations due to the shortening of the equilibrium Van der Waals distance of two molecules to the length of a (significantly shorter) covalent bond. This volumetric shrinkage can have severe influence on the materials’ properties. One strategy to overcome this volumetric shrinkage is the use of expanding monomers that show volumetric expansion during polymerization reactions. Such monomers exhibit cyclic or even oligocyclic structural motifs with a correspondingly dense atomic packing. During the ring-opening reaction of such monomers, linear structures with atomic packing of lower density are formed, which results in volumetric expansion or at least reduced volumetric shrinkage. This review provides a concise overview of expanding monomers with a focus on the elucidation of structure-property relationships. Preceded by a brief introduction of measuring techniques for the quantification of volumetric changes, the most prominent classes of expanding monomers will be presented and discussed, namely cycloalkanes and cycloalkenes, oxacycles, benzoxazines, as well as thiocyclic compounds. Spiroorthoesters, spiroorthocarbonates, cyclic carbonates, and benzoxazines are particularly highlighted.

Design and synthesis of 1,8-Naphthalimide Functionalized Benzothiadiazoles

2021 ◽  
Author(s):  
Rajneesh Misra ◽  
Yogjivan Rout
Keyword(s):  
Ring Opening ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Design And Synthesis ◽  
Cross Coupling Reaction ◽  
Ring Opening Reaction

A series of multi acceptor based push-pull derivatives BTD2–BTD5 were designed and synthesized via Pd-catalyzed Sonogashira cross-coupling reaction followed by [2+2] cycloaddition–electrocyclic ring-opening reaction in which benzothiadiazole (BTD, A1), naphthalimide...

scholarly journals (1R,4S,5S)-5-((3-Hydroxypropyl)amino)-4-((1-Methyl-1H-tetrazol-5-yl)thio)Cyclopent-2-en-1-ol

Molbank ◽  
10.3390/m1199 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1199
Author(s):  
Milene A. G. Fortunato ◽  
Filipa Siopa ◽  
Carlos A. M. Afonso
Keyword(s):  
Spectral Data ◽  
13C Nmr ◽  
Ring Opening ◽  
Environmentally Friendly ◽  
Mass Spectral Data ◽  
Mass Spectral ◽  
Excellent Yield ◽  
Ring Opening Reaction ◽  
Nucleophilic Ring Opening

Using environmentally friendly conditions, the nucleophilic ring-opening reaction of 6-azabicyclo[3.1.0]hex-3-en-2-ol with 1-methyl-1H-tetrazole-5-thiol provided a novel thiol-incorporated aminocyclopentitol, (1R,4S,5S)-5-((3-hydroxypropyl)amino)-4-((1-methyl-1H-tetrazol-5-yl)thio)cyclopent-2-en-1-ol, in excellent yield (95%). The newly synthesized compound was analyzed and characterized via 1H, 13C-NMR, HSQC, and mass spectral data.

ChemInform Abstract: Asymmetric Alkynylative Ring Opening Reaction of Oxabenzonorbornadienes Promoted by Palladium/Silver Cocatalytic System.

ChemInform ◽  
2015 ◽  
Vol 46 (12) ◽  
pp. no-no
Author(s):  
Shanshan Liu ◽  
Sifeng Li ◽  
Hualei Chen ◽  
Qingjing Yang ◽  
Jianbin Xu ◽  
...  
Keyword(s):  
Ring Opening ◽  
Ring Opening Reaction ◽  
Palladium Silver

scholarly journals Remediation of Anthracene-Contaminated Soil with Sophorolipids-SDBS-Na2SiO3 and Treatment of Eluting Wastewater

Water ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 2188
Author(s):  
Wei Li ◽  
Xiaofeng Wang ◽  
Lixiang Shi ◽  
Xianyuan Du ◽  
Zhansheng Wang
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Organic Pollutants ◽  
Aromatic Hydrocarbons ◽  
Contaminated Soil ◽  
Ring Opening ◽  
Single Factor ◽  
Elution Time ◽  
Factor B ◽  
Ring Opening Reaction ◽  
Polycyclic Aromatic

The soil pollution of polycyclic aromatic hydrocarbons (PAHs) is serious in China, which not only affects the living and growing environment of plants and animals but also has a great impact on people’s health. The use of hydrophobic organic compounds to make use of surfactant ectopic elution processing is more convenient and cheaper as a repair scheme and can effectively wash out the polycyclic aromatic hydrocarbons in the soil. Therefore, we mixed sophorolipids:sodium dodecylbenzene sulfonate (SDBS):Na2SiO3 according to the mass ratio of 1:15:150. We explored the influencing factors of high and low concentrations of PAH-contaminated soil using a single factor test and four factors at a two-level factorial design. Then, the elution wastewater was treated by ultrasonic oxidation technology and the alkali-activated sodium persulfate technology. The results showed that: (1) In the single factor test, when the elution time is 8 h, the concentration of the compounded surfactant is 1200 mg/L, the particle size is 60 mesh, the concentration of NaCl is 100 mmol/L, and the concentration of KCl is 50 mmol/L, and the effect of the PAH-contaminated soil eluted by the composite surfactant is the best. Externally added NaCl and KCl salt ions have a more obvious promotion effect on the polycyclic aromatic hydrocarbon-contaminated soil; (2) in the interaction experiment, single factor B (elution time) and D (NaCl concentration) have a significant main effect. There is also a certain interaction between factor A (concentration agent concentration) and factor D, factor B, and factor C (KCl concentration); (3) the treatment of anthracene in the eluate by ultrasonic completely mineralizes the organic pollutants by the thermal and chemical effects produced by the ultrasonic cavitation phenomenon, so that the organic pollutants in the eluate are oxidized and degraded into simple environmentally friendly small molecular substances. When the optimal ultrasonic time is 60 min and the ratio of oxidant to activator is 1:2, the removal rate of contaminants in the eluent can reach 63.7%. At the same time, the turbidity of the eluent is significantly lower than that of the liquid after centrifugal separation, indicating that oxidants can not only remove the pollutants in elution water but also remove the residual soil particulate matter; and (4) by comparing the infrared spectrum of the eluted waste liquid before and after oxidation, it can be seen that during the oxidation process, the inner part of eluent waste liquid underwent a ring-opening reaction, and the ring-opening reaction also occurred in the part of the cyclic ester group of the surfactant, which changed from a ring to non-ring.

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