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Subsequently, star azopolymers were synthesized by polymerization of a difunctional azomonomer, BMA2Az, with resultant Macro-CTA in presence of AIBN as initiator in anisole.
The results establish that the new electrode configuration used in the present investigation can produce good quality coatings by polymerization of a precursor.
Carbon aerogels were prepared by polymerization of a resorcinol formaldehyde mixture using different polymerization catalysts such as: sodium or potassium carbonates, oxalic acid or para-toluenesulfonic acid.
In this work, we examine a series of hydrogel networks formed by polymerization of a commercial diacrylate, polyethylene glycol diacrylate (PEG400DA), and a primary diamine, 4,7,10-trioxa-1,13-tridecanediamine (TTD), in combination with acrylate-functionalized curcumin.
In this article, we develop transparent physical hydrogels by simply casting and reswelling the films of copolymers synthesized by polymerization of a hydrophilic monomer of acrylic acid (AA) with a small fraction of hydrophobic monomer of stearyl acrylate (SA).
Hydrogels were prepared by polymerization of a synthetic macromer, in which the central part is a temperature-sensitive triblock copolymer composed of poly ethylene oxide)–poly(propylene oxide)–poly ethylene oxide), the extension along each end is biodegradable oligo (ε-caprolactone) (oligoCL) terminated with an acrylate group.
Similar(51)
Cross-linking of dextran can be established by derivatization of the polysaccharide with methacryloyl groups followed by polymerization of an aqueous solution of this methacrylated dextran with an initiator system consisting of potassium peroxydisulfate (KPS) and N,N,N′,N′-tetramethylethylenediamine (TEMED).
The block copolymers were also synthesized by RAFT polymerization of A-Pro-OMe using poly(E3VC) as a macro-chain transfer agent (macro-CTA).
TPUs are linear block copolymers obtained by polymerization of three basic components, a diisocyanate and a short (chain extensor) and long-chain diol [1].
Stable polymer latices could be formed by polymerization of microemulsions with an O/W droplet structure.
Almost complete methacrylate conversion (95%) was achieved for hydrogels obtained by polymerization of HyA-MA with a degree of substitution of 15.
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