scholarly journals The Polymerization of MMA and ST to Prepare Material with Gradient Refractive Index in Electric Field

2015 ◽  
Vol 2015 ◽  
pp. 1-6
Author(s):  
Yao Huang ◽  
Daming Wu ◽  
Dongyun Ren ◽  
Qingyun Meng ◽  
Xiaojun Di
Keyword(s):  
Molecular Weight ◽  
Refractive Index ◽  
Electric Field ◽  
Cylindrical Sample ◽  
Electrical Field ◽  
Molecular Weights ◽  
The Matrix ◽  
Gradient Refractive Index ◽  
Scattering Material ◽  
Different Parts

Light scattering material with gradient refractive index was prepared under the electrical field by taking methyl methacrylate (MMA) monomer as the matrix with the addition of a little preheated styrene (ST) and peroxidation benzoin formyl (BPO). The material obtained under electrical field presented different transmittance and molecular weight at different parts of the cylindrical sample along the axis of the direction of electric field which led to the layering phenomenon and gradient refractive index. The disparity of molecular weight between different layers can be as much as 230 thousand. There were several peaks in the figure of GPC test of the sample under electric field. This proved that there were polymers with different molecular weights in the sample. Therefore, it can be concluded that electrical field has a significant effect on polymerization.

Enamel Matrix: Structural Proteins

1979 ◽  
Vol 58 (2_suppl) ◽  
pp. 773-781 ◽  
Author(s):  
J.D. Termine ◽  
D.A. Torchia ◽  
K.M. Conn
Keyword(s):  
Molecular Weight ◽  
Matrix Protein ◽  
Extraction Methods ◽  
Resonance Spectroscopy ◽  
Segmental Motion ◽  
Enamel Matrix ◽  
Molecular Weights ◽  
The Matrix ◽  
Enamel Protein ◽  
Bovine Enamel

Cell-free, fetal bovine enamel tissue was examined intact by high resolution. 13C Fourier transform, nuclear magnetic resonance spectroscopy. Two types of protein chains were observed under these conditions, one exhibiting rapid mobility and accounting for approximately two-thirds of the enamel matrix, while the other exhibited restricted or anisotropic segmental motion and accounted for the remaining third of the matrix. Sequential extraction of this fetal enamel under non-degradative conditions with dissociative solvents yielded two biochemically distinct populations of matrix protein. As expected, the bulk of the matrix consisted of proline-rich amelogenins, although the SDS-gel electrophoresis molecular weights for these proteins were somewhat higher than those reported using other extraction methods. Approximately fifteen percent of the total matrix consisted of much higher molecular weight phosphoproteins (46,000 - 72,000 daltons) whose amino acid composition closely resembled that reported for mature enamel protein. These high molecular weight proteins were tightly bound to the fetal enamel apatite crystallites.

LIGHT-SCATTERING STUDIES OF COPOLYMERS: I. EFFECT OF HETEROGENEITY OF CHAIN COMPOSITION ON THE MOLECULAR WEIGHT

1958 ◽  
Vol 36 (12) ◽  
pp. 1616-1626 ◽  
Author(s):  
W. Bushuk ◽  
H. Benoit
Keyword(s):  
Molecular Weight ◽  
Refractive Index ◽  
Light Scattering ◽  
Average Molecular Weight ◽  
Apparent Molecular Weight ◽  
Scattering Data ◽  
Refractive Index Increment ◽  
Molecular Weights ◽  
Chain Composition ◽  
Total Molecular Weight

The classical light-scattering theory for polymer solutions is extended to solutions of copolymers which may be polydisperse in chain composition as well as in molecular weight. It is shown that much too high molecular weights will result from light-scattering data for copolymers owing to fluctuations in chain composition; the magnitude of this effect increases rapidly as the absolute value of the refractive index increment approaches zero. The methods for determining the usual weight-average molecular weight and polydispersity of composition are described.The theory was tested with experimental results on: (1) a mixture of polystyrene and poly(methylmethacrylate), considered as a copolymer with the highest possible polydispersity of composition; (2) a high conversion, statistical copolymer of styrene and methylmethacrylate (copolymer I); and (3) a block copolymer of the same monomers (copolymer II). The apparent molecular weight for copolymer I (Mw = 1.83 × 105) varied markedly with refractive index increment in much the same way as the total molecular weight for the mixture. The molecular weight of copolymer II (Mw = 1.20 × 106) remained essentially constant in the same series of solvents. The polydispersities of composition obtained were 0.72 and 0.05 for copolymer I and II respectively compared with the maximum possible value equal to 1.0.

scholarly journals Nonlinear Electrical Properties and Field Dependency of BST and Nano-ZnO-Doped Silicone Rubber Composites

Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3153 ◽  
Author(s):  
Juyi Guo ◽  
Xilin Wang ◽  
Zhidong Jia ◽  
Jun Wang ◽  
Chuan Chen
Keyword(s):  
Electrical Properties ◽  
Electric Field ◽  
Silicone Rubber ◽  
Distribution System ◽  
Interfacial Area ◽  
Rubber Composites ◽  
Electrical Field ◽  
Field Dependency ◽  
The Matrix ◽  
Transmission And Distribution

Recently, composite materials with nonlinear dielectric or resistive properties performed well in electric field homogenization and space charge suppression in a high voltage transmission and distribution system. For the purpose of obtaining insulation materials with desirable dielectric and electrical resistance properties, we investigated several fillers with nonlinear electrical properties doped in silicon rubber composites, and their dependency on the temperature and field. The samples of silicone rubber composites with different components were prepared using barium strontium titanate (BST) and zinc oxide (ZnO) as the filler, and high temperature vulcanized silicone rubber (SiR) as the matrix. The investigations revealed that the BST-doped samples showed different dielectric properties compared to ZnO-doped composites, with an increase in the electric field, which was nonlinear. The resistivity of both doped samples was similar. Results demonstrated that it was possible to achieve higher values of permittivity, and lower values of tanδ and resistivity, with respect to unfilled silicone rubber composites over a wide electrical field and temperature range. Discussion of the results attributes these important functional behaviours to the spontaneous polarization of nonlinear nanoparticles and the interaction between the SiR chains and the nonlinear nanoparticles at the interfacial area.

LIGHT-SCATTERING APPARATUS AND TECHNIQUES FOR MEASURING MOLECULAR WEIGHTS OF HIGH POLYMERS

1949 ◽  
Vol 27b (10) ◽  
pp. 791-806 ◽  
Author(s):  
H. J. Hadow ◽  
H. Sheffer ◽  
J. C. Hyde
Keyword(s):  
Molecular Weight ◽  
Refractive Index ◽  
Light Scattering ◽  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Scattered Light ◽  
Molecular Weights ◽  
Sources Of Error ◽  
Reduced Intensity

Apparatus is described for the measurement of small amounts of scattered light, dissymmetry of radiation, depolarization, and very small refractive index differences. Methods of calibration are critically examined. Benzene was adopted as a turbidity standard. Measurements were made on fractionated polystyrene of known molecular weight and on bovine serum albumin solutions. Values of the reduced intensity for benzene were obtained:[Formula: see text]Degree and sources of error are discussed

Investigation by HPLC of the Catabolism of Recombinant Tissue Plasminogen Activator in the Rat

1988 ◽  
Vol 60 (01) ◽  
pp. 107-112 ◽  
Author(s):  
Roy Harris ◽  
Louis Garcia Frade ◽  
Lesley J Creighton ◽  
Paul S Gascoine ◽  
Maher M Alexandroni ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Plasminogen Activator ◽  
Tissue Plasminogen Activator ◽  
Half Life ◽  
Recombinant Tissue Plasminogen Activator ◽  
Rat Plasma ◽  
High Molecular Weight Complex ◽  
Molecular Weights ◽  
Major Activity ◽  
Tissue Plasminogen

SummaryThe catabolism of recombinant tissue plasminogen activator (rt-PA) was investigated after injection of radiolabelled material into rats. Both Iodogen and Chloramine T iodination procedures yielded similar biological activity loss in the resultant labelled rt-PA and had half lives in the rat circulation of 1 and 3 min respectively. Complex formation of rt-PA was investigated by HPLC gel exclusion (TSK G3000 SW) fractionation of rat plasma samples taken 1-2 min after 125I-rt-PA injection. A series of radiolabelled complexes of varying molecular weights were found. However, 60% of the counts were associated with a single large molecular weight complex (350–500 kDa) which was undetectable by immunologically based assays (ELISA and BIA) and showed only low activity with a functional promoter-type t-PA assay. Two major activity peaks in the HPLC fractions were associated with Tree t-PA and a complex having a molecular weight of ̴ 180 kDa. HPLC fractionation to produce these three peaks at various timed intervals after injection of 125I-rt-PA showed each to have a similar initial rate half life in the rat circulation of 4-5 min. The function of these complexes as yet is unclear but since a high proportion of rt-PA is associated with a high molecular weight complex with a short half life in the rat, we suggest that the formation of this complex may be a mechanism by which t-PA activity is initially regulated and finally cleared from the rat circulation.

Permeability Enhancing and Chemotactic Activities of Lower Molecular Weight Degradation Products of Human Fibrinogen

1981 ◽  
Vol 45 (01) ◽  
pp. 090-094 ◽  
Author(s):  
Katsuo Sueishi ◽  
Shigeru Nanno ◽  
Kenzo Tanaka
Keyword(s):  
Molecular Weight ◽  
Degradation Products ◽  
Electron Microscopic Observation ◽  
Chemotactic Activity ◽  
Lower Molecular Weight ◽  
Electron Microscopic ◽  
Human Fibrinogen ◽  
Rabbit Skin ◽  
Molecular Weights ◽  
Active Fragments

SummaryFibrinogen degradation products were investigated for leukocyte chemotactic activity and for enhancement of vascular permeability. Both activities increased progressively with plasmin digestion of fibrinogen. Active fragments were partially purified from 24 hr-plasmin digests. Molecular weights of the permeability increasing and chemotactic activity fractions were 25,000-15,000 and 25,000 respectively. Both fractions had much higher activities than the fragment X, Y, D or E. Electron microscopic observation of the small blood vessels in rabbit skin correlated increased permeability with the formation of characteristic gaps between adjoining endothelial cells and their contraction.These findings suggest that lower molecular weight degradation products of fibrinogen may be influential in contributing to granulocytic infiltration and enhanced permeability in lesions characterized by deposits of fibrin and/or fibrinogen.

Toxicity of Heparinoids, with Special Reference to the Precipitation of Fibrinogen

1964 ◽  
Vol 12 (01) ◽  
pp. 232-261 ◽  
Author(s):  
S Sasaki ◽  
T Takemoto ◽  
S Oka
Keyword(s):  
Molecular Weight ◽  
Dextran Sulfate ◽  
Anticoagulant Activity ◽  
Molecular Structures ◽  
Severe Reaction ◽  
Clinical Use ◽  
Molecular Weights ◽  
Close Relationship

SummaryTo demonstrate whether the intravascular precipitation of fibrinogen is responsible for the toxicity of heparinoid, the relation between the toxicity of heparinoid in vivo and the precipitation of fibrinogen in vitro was investigated, using dextran sulfate of various molecular weights and various heparinoids.1. There are close relationships between the molecular weight of dextran sulfate, its toxicity, and the quantity of fibrinogen precipitated.2. The close relationship between the toxicity and the precipitation of fibrinogen found for dextran sulfate holds good for other heparinoids regardless of their molecular structures.3. Histological findings suggest strongly that the pathological changes produced with dextran sulfate are caused primarily by the intravascular precipitates with occlusion of the capillaries.From these facts, it is concluded that the precipitates of fibrinogen with heparinoid may be the cause or at least the major cause of the toxicity of heparinoid.4. The most suitable molecular weight of dextran sulfate for clinical use was found to be 5,300 ~ 6,700, from the maximum value of the product (LD50 · Anticoagulant activity). This product (LD50 · Anticoagulant activity) can be employed generally to assess the comparative merits of various heparinoids.5. Clinical use of the dextran sulfate prepared on this basis gave satisfactory results. No severe reaction was observed. However, two delayed reactions, alopecia and thrombocytopenia, were observed. These two reactions seem to come from the cause other than intravascular precipitation.

Molecular Weights of Factor VIII (AHF) and Factor IX (PTC) by Electron Irradiation

1962 ◽  
Vol 08 (02) ◽  
pp. 270-275 ◽  
Author(s):  
David L Aronson ◽  
John W Preiss ◽  
Michael W Mosesson
Keyword(s):  
Molecular Weight ◽  
Factor Viii ◽  
Electron Irradiation ◽  
Factor Ix ◽  
Molecular Weights

SummaryThe molecular weights of AHF (factor VIII) and of PTC (factor IX) have been estimated by their sensitivity to inactivation by 7 kilovolt electrons. The molecular weight of AHF was found to be 180 000 by this method and that of PTC was found to be 110 000.

Purine nucleoside phosphorylase: Isolation and characterization

1990 ◽  
Vol 55 (12) ◽  
pp. 2987-2999 ◽  
Author(s):  
Katarina Šedivá ◽  
Ivan Votruba ◽  
Antonín Holý ◽  
Ivan Rosenberg
Keyword(s):  
Molecular Weight ◽  
Purine Nucleoside Phosphorylase ◽  
Purine Nucleoside ◽  
Leukemia Cells ◽  
Ph Optimum ◽  
Nucleoside Phosphorylase ◽  
Isolation And Characterization ◽  
Reaction Proceeds ◽  
The Matrix ◽  
Sepharose 4B

Purine nucleoside phosphorylase (PNP) from mouse leukemia cells L1210 was purified to homogeneity by a combination of ion exchange and affinity chromatography using AE-Sepharose 4B and 9-(p-succinylaminobenzyl)hypoxanthine as the matrix and the ligand, respectively. The native enzyme has a molecular weight of 104 000 and consists of three subunits of equal molecular weight of 34 000. The results of isoelectric focusing showed that the enzyme is considerably microheterogeneous over the pI-range 4.0-5.8 and most likely consists of eight isozymes. The temperature and pH-optimum of phosphorolysis, purine nucleoside synthesis and also of transribosylation is identical, namely 55 °C and pH 7.4. The transribosylation reaction proceeds in the presence of phosphate only. The following Km-values (μmol l-1) were determined for phosphorolysis: inosine 40, 2'-deoxyinosine 47, guanosine 27, 2'-deoxyguanosine 32. The Km-values (μmol l-1) of purine riboside and deoxyriboside synthesis are lower than the values for phosphorolysis (hypoxanthine 18 and 34, resp., guanine 8 and 11, resp.). An affinity lower by one order shows PNP for (-D-ribose-1-phosphate, (-D-2-deoxyribose-1-phosphate (Km = 200 μmol l-1 in both cases) and phosphate (Km = 805 μmol l-1). The substrate specificity of the enzyme was also studied: positions N(1), C(2) and C(8) are decisive for the binding of the substrate (purine nucleoside).

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