Polymerization of Chloroprene in the Presence of Organometallic Compounds: The System Chloroprene-Butyllithium

1965 ◽  
Vol 38 (4) ◽  
pp. 991-998
Author(s):  
B. L. Erusalimskii ◽  
I. G. Krasnoselskaya ◽  
V. V. Mazurek

Abstract In the polymerization of chloroprene in the presence of butyl lithium, a substantial role is ascribed to reactions of deactivation of growing chains, which prevents the possibility of attaining a high degree of conversion. Kinetic data indicate the anionic mechanism of the process.

Author(s):  
Ryan R. Holmes ◽  
Jennifer R. Melander ◽  
Rachel A. Weiler ◽  
Thomas P. Schuman ◽  
Kathleen V. Kilway ◽  
...  

The aesthetic appeal of composite-resin restoratives promotes their use, however their functional life is significantly shorter when compared to their metal counterparts.1 One possible reason is the effect of polymerization stress on marginal integrity. Shrinkage of the composite, and its associated stress, has been found to cause gap formation and stress interactions between the restorative and the adhesive. These gaps offer an ideal niche for bacteria, and, when compounded by the mechanical strain of chewing, can lead to premature failure of the restorative.2,3 Additionally, it is well known that incomplete conversion of the double bonds occurs during methacrylate polymerizations.4–7 A high degree of conversion is needed to prevent the presence of potentially hazardous monomers.8


2021 ◽  
Vol 24 (4) ◽  
Author(s):  
Peterson Oliveira Boeira ◽  
Mateus De Azevedo Kinalski ◽  
Mateus Bertolini Fernandes dos Santos ◽  
Rafael Ratto de Moraes ◽  
Giana Silveira Lima

Objective: of this study was to characterize and correlate the absorption spectra of three photoinitiators [camphorquinone (CQ), diphenyl(2,4,6-trimethylbenzoyl) phosphine oxide (TPO) and phenylbis (2,4,6-trimethylbenzoyl)-phosphine oxide (BAPO)], using second or third-generation light curing units (LCU), and to evaluate the degree of conversion and the physical properties of an experimental resin adhesive.  Material and methods: Second-generation (Radii-cal® and Emitter D®) and third-generation (Valo® Cordless and Bluephase N®) LCU were assessed regarding spectrum and irradiance rate of emitted light. Also, the photoinitiators (CQ, TPO and BAPO) were characterized by a light absorption spectrum assessed by UV-Vis spectroscopy, degree of conversion and yellowing effect. Statistical analyzes considered two-way ANOVA and post-hoc Tukey test.  Results: BAPO presented higher reactivity compared to TPO. Regarding degree of conversion of the photoinitiators activated by different light-curing units, the Emitter D® device promoted a high degree of conversion. BAPO presented the highest yellowing effect values. Conclusions: The emission and absorption characteristics of the photoinitiators were different. The polymerization reaction activated by the second-generation light-curing unit was reduced when using an experimental resin with photoinitiator TPO, and the third-generation light-curing unit showed a higher polymerization potential regardless of the photoinitiator. Keywords Light-curing of dental adhesives;  Photoinitiators dental; Curing lights dental.


2019 ◽  
Vol 109 ◽  
pp. 00025
Author(s):  
Liliya Frolova ◽  
Tetyana Butyrina ◽  
Yurii Galivets

In this work we prove the possibility of blast furnace slag use as a basis for green, black, brown and orange pigments. We presented kinetic characteristics of the process, as well as the main characteristics of the products obtained. We found that a high degree of conversion is provided by both chemical reaction and adsorption. Through microscopic analysis we identified pigment dispersion. We worked out technological scheme of the process.


2020 ◽  
Vol 45 (5) ◽  
pp. 556-566 ◽  
Author(s):  
A Tichy ◽  
K Hosaka ◽  
A Abdou ◽  
M Nakajima ◽  
J Tagami

Clinical Relevance The degree of conversion of contemporary universal adhesives positively correlates with the bond strength to dentin. The correlation is more marked after thermocycling, suggesting that a high degree of conversion is required for long-term dentin bonding durability. SUMMARY Purpose: The objectives of this study were to evaluate the micro-tensile bond strength (μTBS) of five contemporary universal adhesives to dentin after 24 hours and thermocycling (TC), to measure their degrees of conversion (DC) and to test the correlation between μTBS and DC. Methods and Materials: Four commercially available universal adhesives, Prime&Bond universal (PBU), Ecosite Bond (EB), G-Premio Bond (GPB), and Clearfil Universal Bond Quick (UBQ), and one experimental adhesive, UBQ without an amide monomer (UBQ-A), were used in this study. For the μTBS test, midcoronal dentin of 50 human molars was exposed, ground using 600-grit SiC paper, and the adhesives were applied according to the manufacturers’ instructions. After resin-composite buildup and 24-hour water storage, one-half of the specimens were subjected to 15,000 thermal cycles. The specimens were sectioned into beams and stressed in tension at a crosshead speed of 1 mm/min until failure. The DC of adhesives applied to dentin was evaluated using attenuated total reflectance Fourier-transform infrared spectroscopy immediately after light-curing. All data were statistically analyzed at a significance level of 0.05. Results: The highest μTBSs were obtained with UBQ, UBQ-A, and PBU, which were not significantly different from each other both after 24 hours and TC. The μTBS of GPB was lower compared with the aforementioned adhesives, but significantly only after TC, and the lowest μTBSs were obtained with EB. TC did not affect the μTBSs of UBQ, UBQ-A, and PBU significantly, but a significant decrease was observed with GPB and EB. The highest DC was obtained with PBU and UBQ, followed by 2-hydroxyethyl methacrylate–rich adhesives UBQ-A and EB, which exhibited significantly lower DCs. The DC of GPB could not be determined because the reference peak at 1608 cm−1 was not detected in its spectra. A significant positive correlation was shown between μTBS and DC after 24 hours (r=0.716) and TC (r=0.856). Conclusion: μTBS and DC were positively correlated, more markedly after TC, which suggests that DC may be an important factor for bond durability.


1985 ◽  
Vol 40 (11) ◽  
pp. 1490-1494 ◽  
Author(s):  
Herbert Schumann ◽  
Gerald Jeske

Tricyclopentadienylneodymium and -lutetium react with sec-butyl lithium and terf-butyl lithium to form sec-butyl- and tert-butyl(dicyclopentadienyl)neodymium and -lutetium, which decompose to the corresponding dicyclopentadienyllanthanide hydride complexes. Dicyclopentadienyl-bis-(trimethylsilyl)methylsamarium and -lutetium are made from dicyclopentadienylsamarium or -lutetium chloride and bis(trimethylsilyl)methyl lithium. They react with hydrogen to form the corresponding dicyclopentadienyllanthanide hydride complexes.


1939 ◽  
Vol 12 (3) ◽  
pp. 556-567 ◽  
Author(s):  
H. P. Stevens ◽  
C. J. Miller

Abstract Boron trifluoride or materials which give rise thereto effect a “cyclization” of rubber in solution: that is, the product is less unsaturated than the original rubber. A particular degree of conversion has been shown to give a tough material, which produces strongly adherent films possessing a high degree of alkali-resistance. When used as a paint medium the material acts as an unsaponifiable “breather” and pigment protector, allowing (unlike “sealers”) the passage of aqueous solutions. For this reason it appears suitable for use on plaster and concrete. Analysis of the purified product indicates appreciable oxidation at some stage and it may be further oxidized by aging at raised temperature or by reagents such as hydrogen peroxide. The oxidation products are not identical. The conversion product yields also a hard vulcanized product resembling hard vulcanized rubber, but less thermoplastic and containing less sulfur than hard rubber produced under the same conditions. This work has been carried out on behalf of the Rubber Producers' Research Association, to whom the authors are indebted for permission to publish.


Author(s):  
Ewa Rząd ◽  
Tomasz Dudziak ◽  
Tomasz Polczyk ◽  
Łukasz Boroń ◽  
Paweł Figiel ◽  
...  

AbstractThis study was carried out to evaluate a series of ceramic coatings in a sulfidation atmosphere containing 99% synthetic air and 1% H2S (vol.%) under a flow rate of 50 mL/min. The study was carried out at 773.15 K for 336 hours (heating rate 278.15 K/min). Chemically resistant glass enamels based on SiO2-B2O3-TiO2-Na2O compounds were deposited on the surface of 16Mo3 (16M) low-alloyed steel. Kinetic data were recorded periodically every 168 hours; macro- and microanalyses using scanning electron microscopy (SEM), phase analyses using x-ray diffractometry (XRD) and chemical composition using energy-dispersive x-ray spectrometry along with EDS x-ray mappings were carried out to observe the degradation process of the sulfidized coatings. The results indicated that some of the ceramic coatings exposed in the harsh atmosphere at 773.15 K for 336 hours showed a high degree of protection.


2000 ◽  
Vol 4 (2) ◽  
pp. 145-164 ◽  
Author(s):  
Moishe garfinkle

The Natural Path approach to chemical reaction kinetics was developed to bridge the considerable gap between the Mass Action mechanistic approach and the non-mechanistic irreversible thermodynamic approach. The Natural Path approach can correlate empirical kinetic data with a high degree precision, as least equal to that achievable by the Mass-Action rate equations, but without recourse mechanistic considerations. The reaction velocities arising from the particular rate equation chosen by kineticists to best represent the kinetic behavior of a chemical reaction are the natural outcome of the Natural Path approach. Moreover, by virtue of its thermodynamic roots, equilibrium thermodynamic functions can be extracted from reaction kinetic data with considerable accuracy. These results support the intrinsic validity of the Natural Path approach.


2017 ◽  
Vol 6 (1) ◽  
pp. 33 ◽  
Author(s):  
Sefty Aryani Harahap ◽  
Yosi Kusuma Eriwati

A recent technology of Bulk fill composite resin has been developed to save manipulation time. Bulk fill composite resinhas been claimed to have depth of cure up to 4 mm with a high degree of conversion. This paper will evaluate the role of bulk fill composite resin’s composition in increasingits degree of conversion. The degree of conversion is the percentage of carbon double bonds that were converted into single bonds as a result of polymerization. It is determined by its composition that contained filler, resin matrix and the photoinitiator. With the development and modifications of the composition, the bulk fill compositeresin  can be obtained a high degree of conversion so that the expected properties can be achieved.


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