Search results for " polymerization"

The photochemical rearrangement of polymeric N-(1-pyridinio) amidates. A novel, aqueous photoresist system

1988

The use of utraviolet-visible spectrophotometry in the determination of average properties of nonylphenol ethylene oxide condensates

1983

Ultraviolet spectrophotometry is usd in the determination of average molecular weight (M), average degree of polymerization (X), the hydrophilic-lipophilic balance (HLB) and ethylene oxide percentage of nonylphenol ethylene oxide condensates. The method is based on determination of the absorptivity a, expressed in g lt-1 cm−1, from the absorbances measured at 275 nm for a series of dilutions of an aqeuous ethanolic solution (60:40, v/v/) of a given product, followed by numerical interpolation of this value in the expression a = f(HLB), log a = f(log M), and log a = f(log X). These expressions are obtained from reference samples or samples previously analyzed. The proposed method gives relat…

Synthesis of Water-Soluble Copolymers Carrying Long-Chain (C12 to C30 ) Aliphatic Moieties

2011

Water-soluble copolymers from mono-1-alkyl itaconates and N-vinyl-2-pyrrolidone are synthesized and characterized. Themono-1-alkyl itaconates are prepared from itaconic anhydride and the related alcohol: 1-dodecanol, 1-octadecanol, 1-docosanol, and 1-triacontanol. The mono-1-triacontyl itaconate is synthesized fromplant growth regulator policosanols extracted from Agave fourcrouydes, where 1-triacontanol is the major product. The reactivity ratios, calculated according to the Mao-Huglin method for copolymerizations conducted to medium-high conversions, indicate a tendency toward alternation for all copolymerization reactions. Water solubility of copolymers is provided as a function of copol…

Reduced protein adsorption on plastics via direct plasma deposition of triethylene glycol monoallyl ether

1997

The direct plasma-induced deposition of tri(ethylene glycol) monoallyl ether is reported. RF plasma polymerization of this monomer was carried out under both continuous wave (CW) and pulsed plasma operation. The major focus of this work was optimization of the degree of retention of the C-O-C bonds of the starting monomer during the deposition process. This successfully was accomplished using low RF power during the CW runs and low RF duty cycles during the pulsed plasma experiments. Spectroscopic analysis of the plasma films revealed a strong dependence of film composition on the RF power and duty cycles employed. In particular, an unusually high level of film chemistry compositional contr…

Novel water-swellable beads based on an acryloylated polyaspartamide

2001

Spherical polymeric microparticles have been prepared by a reverse-phase suspension polymerization technique. The starting polymer was α,β-poly (N-2-hydroxyethyl)-dl-aspartamide (PHEA) partially functionalised with glycidylmethacrylate (GMA) in order to introduce reactive vinyl groups in the side chain. The PHEA–GMA copolymer obtained (PHG) was cross-linked in a mixture of water/hexane–carbon tetrachloride in the presence of sorbitan trioleate (Span 85) as surfactant and ammonium persulfate/N,N,N′,N′-tetramethylethylenediamine as initiator system. The reaction was also carried out in the presence of N,N′-dimethylacrylamide as comonomer or N,N′-ethylenebisacrylamide as a cross-linking agent.…

Design, Synthesis and Evaluation of Enzyme-Responsive Fluorogenic Probes Based on Pyridine-Flanked Diketopyrrolopyrrole Dyes

2020

The ever-growing demand for fluorogenic dyes usable in the rapid construction of analyte-responsive fluorescent probes, has recently contributed to a revival of interest in the chemistry of diketopyrrolopyrrole (DPP) pigments. In this context, we have explored the potential of symmetrical and unsymmetrical DPP derivatives bearing two or one 4-pyridyl substituents acting as optically tunable group(s). The unique fluorogenic behavior of these molecules, closely linked to N-substitution/charge state of their pyridine unit (i.e., neutral pyridine or cationic pyridinium), has been used to design DPP-based fluorescent probes for detection of hypoxia-related redox enzymes and penicillin G acylase …

Novel pathways for the preparation of mesoporous MCM-41 materials: control of porosity and morphology

1999

Two novel synthesis routes for the preparation of mesoporous MCM-41 materials are introduced. Both methods use tetra-n-alkoxysilanes such as tetraethoxysilane (TEOS) or tetra-n-propoxysilane (TPS) as a silica source which are added to an aqueous solution of a cationic surfactant in the presence of ammonia as catalyst. In this study, n-alkyltrimethylammonium bromides and n-alkylpyridinium chlorides were employed as templates. The addition of an alcohol (e.g. ethanol or isopropanol) leads to a homogeneous system which allows the formation of spherical MCM-41 particles. The main advantages of these methods are short reaction times, excellent reproducibility and easy preparation of large batche…

1989

The reaction kinetics for the group transfer polymerization (GTP) of tert-butyl methacrylate (TBMA) using a silyl ketene acetal initiator and a nucleophilic catalyst are investigated. The reaction is shown to be of first order in both monomer and catalyst concentrations. The “livingness” of this system appears to be influenced by the reaction temperature. At temperatures above −20°C, deactivation is observed, with its severity increasing with increasing temperature. This deactivation is attributed to a depletion of catalyst by side reactions. It was demonstrated that reactivation is made possible by the addition of more catalyst. This result is in contrast to the anionic polymerization of T…

1981

The anionic polymerization of tert-butyl methacrylate (TBMA) in tetrahydrofuran, using Na+ and Cs+ as counterions proceeds without side reactions even at room temperature. The resulting molecular weight distributions are nearly monodisperse (Mw/Mn ⩽ 1,01). The rate constants for the propagation of ion pairs were measured in the range from + 15 to −100°C. The Arrhenius plots are linear, but different for the two counterions, resulting in the following numerical values for the frequency exponent A and the activation energy Ea: A = 8,5 and Ea = 7,2 kcal/mol = 30 kJ/mol for Na+; A = 9,5 and Ea = 5,6 kcal/mol = 23 kJ/mol for Cs+. The difference between the counterions, which is in contrast to th…

ELECTROCHEMICALLY ASSISTED ATOM TRANSFER RADICAL GRAFT COPOLYMERIZATION. PRELIMINARY STUDIES

2012

Atom transfer radical polymerization (ATRP) is a versatile technique for exerting precise control over polymer molecular weights, molecular weight distributions, and complex architectures. It has been recently shown that an externally applied electrochemical potential can reversibly activate the copper catalyst for this process by a one-electron reduction of an initially added air-stable cubric species (Cu(II)/Ligand) [1-2]. In particular Gennaro and co-authors have shown that the polymerization kinetic can be changed modulating the external potential [1-2]. In the last years, an increasing interest has been devoted to synthesis of graft copolymers obtained from commercial polymers for inco…