Mechanisms initiator systems

Ammonia H2O2 Initiation. The lower molecular weight grades (K-15 and K-30) ofPVP ate prepared industrially with an ammonia /H O initiation system. Such products ate the standards for the pharmaceutical industry and conform to the various national pharmacopeias. Several papers have appeared concerning the mechanism of this polymerization (15). 

The polysulfide impression materials can be formulated to have a wide range of physical and chemical characteristics by modifying the base (polysulfide portion), and/or the initiator system. Further changes may be obtained by varying the proportion of the base to the catalyst in the final mix. Characteristics varied by these mechanisms include viscosity control from thin fluid mixes to heavy thixotropic mixes, setting-time control, and control of the set-mbber hardness from a Shore A Durometer scale of 20 to 60. Variations in strength, toughness, and elasticity can also be achieved. 

Simplified nitrile mbber polymerization recipes are shown in Table 2 for "cold" and "hot" polymerization. Typically, cold polymerization is carried out at 5°C and hot at 30°C. The original technology for emulsion polymerization was similar to the 30°C recipe, and the redox initiator system that allowed polymerization at lower temperature was developed shortiy after World War II. The latter uses a reducing agent to activate the hydroperoxide initiator and soluble iron to reactivate the system by a reduction—oxidation mechanism as the iron cycles between its ferrous and ferric states. 

Reaction Mechanism of Vinyl Polymerization with Amine in Redox and Photo-Induced Charge-Transfer Initiation Systems... 

Organic peroxide-aromatic tertiary amine system is a well-known organic redox system 1]. The typical examples are benzoyl peroxide(BPO)-N,N-dimethylani-line(DMA) and BPO-DMT(N,N-dimethyl-p-toluidine) systems. The binary initiation system has been used in vinyl polymerization in dental acrylic resins and composite resins [2] and in bone cement [3]. Many papers have reported the initiation reaction of these systems for several decades, but the initiation mechanism is still not unified and in controversy [4,5]. Another kind of organic redox system consists of organic hydroperoxide and an aromatic tertiary amine system such as cumene hydroperoxide(CHP)-DMT is used in anaerobic adhesives [6]. Much less attention has been paid to this redox system and its initiation mechanism. A water-soluble peroxide such as persulfate and amine systems have been used in industrial aqueous solution and emulsion polymerization [7-10], yet the initiation mechanism has not been proposed in detail until recently [5]. In order to clarify the structural effect of peroxides and amines including functional monomers containing an amino group, a polymerizable amine, on the redox-initiated polymerization of vinyl monomers and its initiation mechanism, a series of studies have been carried out in our laboratory. 

A substantial number of photo-induced charge transfer polymerizations have been known to proceed through N-vinylcarbazole (VCZ) as an electron-donor monomer, but much less attention was paid to the polymerization of acrylic monomer as an electron receptor in the presence of amine as donor. The photo-induced charge-transfer polymerization of electron-attracting monomers, such as methyl acrylate(MA) and acrylonitrile (AN), have been recently studied [4]. In this paper, some results of our research on the reaction mechanism of vinyl polymerization with amine in redox and photo-induced charge transfer initiation systems are reviewed. 

The polymers initiated by BP amines were found to contain about one amino end group per molecular chain. It is reasonable to consider that the combination of BP and such polymers will initiate further polymerization of vinyl monomers. We investigated the photopolymerization of MMA with BP-PMMA bearing an anilino end group as the initiation system and found an increase of the molecular weight from GPC and viscometrical measurement [91]. This system can also initiate the photopolymerization of AN to form a block copolymer, which was characterized by GPC, elemental analysis, and IR spectra. The mechanism proposed is as follows ... 

The initiating radicals are assumed to be SCN, ONO or N3 free radicals. Tris oxalate-ferrate-amine anion salt complexes have been studied as photoinitiators (A = 436 nm) of acrylamide polymer [48]. In this initiating system it is proposed that the CO2 radical anion found in the primary photolytic process reacts with iodonium salt (usually diphenyl iodonium chloride salt) by an electron transfer mechanism to give photoactive initiating phenyl radicals by the following reaction machanism ... 

From this initiation mechanism, the important role of the aldehyde group in the reaction mechanism of 1,2-diol and l-amino-2-hydroxy compound and Ce(IV) ion initiation systems can again be seen. 

The early history of redox initiation has been described by Bacon.23 The subject has also been reviewed by Misra and Bajpai,207 Bamford298 and Sarac.2,0 The mechanism of redox initiation is usually bimolecular and involves a single electron transfer as the essential feature of the mechanism that distinguishes it from other initiation processes. Redox initiation systems are in common use when initiation is required at or below ambient temperature and drey are frequently used for initiation of emulsion polymerization. 

The processes described in this section should be contrasted with RAFT polymerization (Section 9.5.3), which can involve the use of similar thioearbonylthio compounds. A. A -dialkyl dithiocarbamates have very low transfer constants in polymerizations of S and (mctb)acrylatcs and arc not effective in RAFT polymerization of these monomers. However, /V,A -dialkyl dithiocarbamates have been successfully used in RAFT polymerization of VAc. Certain O-alkyl xanthates have been successfully used to control RAFT polymerizations of VAc, acrylates and S. The failure of the earlier experiments using these reagents and monomers to provide narrow molecular weight distributions by a RAFT mechanism can he attributed to the use of non-ideal reaction conditions and reagent choice. A two part photo-initiator system comprising a mixture of a benzyl dithiocarhamate and a dithiuram disulfide has also been described and provides better control (narrower molecular weight distributions).43... 

Scheme 5. Mechanism of isobutylene polymerization with the H(CH3) iSiCH2CH2

A relation between A jjv and molecular weight controlling mechanisms was discovered and the effect of initiator system, solvent and temperature on a mv was explained. The present work has led to an understanding of the effect of counteranion on PIB molecular weight. These studies provide better insight into the detailed mechanism of isobutylene polymerization, in particular into the initiation and the molecular weight controlling events. 

Kennedy and Rengachary4 similarly determined AEmv, Mv and M for PIB prepared by a host of alkylaluminum initiator systems. Recently, Cesca and coworkers20 have used Mv data to determine the mechanism of isobutylene polymerization using the Cl2/Et2AlCl/MeCl system. 

Studying the reaction orders for every reagent and initiating system Fe(CO)5 + DMF (1 3) showed that in this specific reaction the radical mechanism of a chain transfer was more probable. However, in other reactions a mechanism can change depending on the reagents nature and their capability of forming more or less stable complexes with Fe(CO)5. 

When energy transfer takes place via an exchange mechanism, the system obeys Wigner s spin rule.(32) If and xs are the initial spin quantum numbers... 

The initial ventilation rate for the whole house was typically 0.2 h 1. When the mechanical ventilation system was running, the supply and exhaust flow rates were in the range 250-300 m3 h"1, providing a ventilation rate of about 0.8 h-1 in ventilated rooms. 

While there have been several studies on the synthesis of block copolymers and on the molecular weight evolution during solution as well as bulk polymerizations (initiated by iniferters), there have been only a few studies of the rate behavior and kinetic parameters of bulk polymerizations initiated by iniferters. In this paper, the kinetics and rate behavior of a two-component initiation system that produces an in situ living radical polymerization are discussed. Also, a model that incorporates the effect of diffusion limitations on the kinetic constants is proposed and used to enhance understanding of the living radical polymerization mechanism. 

As cardiac function decreases after myocardial injury, the heart relies on the following compensatory mechanisms (1) tachycardia and increased contractility through sympathetic nervous system activation (2) the Frank-Starling mechanism, whereby increased preload increases stroke volume (3) vasoconstriction and (4) ventricular hypertrophy and remodeling. Although these compensatory mechanisms initially maintain cardiac function, they are responsible for the symptoms of HF and contribute to disease progression. 

Classical systems evolve from initial mechanical states that may, in principle, be known completely. The systems of classical ensembles have well-defined mechanical states and the initial system is always found in one of these states, although it is not known which one. In quantum mechanics however, the state of a system, including its initial state, is represented by a... 

Fig. 2 A,B. Application of cationic polymerization for neobiopolymer synthesis. A Mechanism of polymerization. B Minoda s use of Higashimura and Sawamoto s initiating system to generate a protected glucose-substituted polymer...

Chojnowski and co-workers have studied the polymerization of octamethyltetrasila-l,4-dioxane, a monomer more basic than cyclosiloxanes, which is capable of forming more stable oxonium ions, and thus being a useful model to study the role of silyloxonium ions.150-152 In recent work, these authors used Olah s initiating system and observed the formation of oxonium ion and its transformation to the corresponding tertiary silyloxonium ion at the chain ends.153 The 29Si NMR spectroscopic data and theoretical calculations were consistent with the postulated mechanism. Stannett and co-workers studied an unconventional process of radiation-initiated polymerization of cyclic siloxanes and proposed a mechanism involving the intermediate formation of silicenium ions solvated by the siloxane... 

The Mn + complexed ions appear to be the most selective and efficient initiator system for grafting to polysaccharides so far described. The mechanism of the initiation reaction has been studied in our laboratories by model experiments and ESR spectroscopy. There are two possible reactions indicated. Bond cleavage of a vicinal diol according to reaction (22) is one possibility. Another and faster reaction with Mn3+ giving radicals appears to be oxidation of aldehyde groups (24) to alkoxy radicals ... 

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