scholarly journals Molecular mobility in bulk and in near-surface nano-layers of ultra-high-molecular-weight polyethylene

2021 ◽  
Vol 2103 (1) ◽  
pp. 012227
Author(s):  
V I Siklitsky ◽  
A K Gladkov ◽  
E M Ivan’kova ◽  
D V Lebedev ◽  
L P Myasnikova ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Molecular Mobility ◽  
High Frequency ◽  
Segmental Mobility ◽  
Near Surface ◽  
Molecular Weights ◽  
Temperature Position ◽  
Powder Particles ◽  
Crystallization Conditions ◽  
Ultra High Molecular Weight

Abstract A comparative study of molecular dynamics in near-surface nanolayers and in a bulk of polyethylene is presented. Molecular mobility in near-surface nanolayers of polyethylene reactor powders and melt-crystallized films of various molecular weights prepared in different crystallization conditions were studied with the help of thermoluminescence technique using high frequency glow dicharge Ar plasma for surface activation. Molecular mobility in a bulk of the same samples was investigated by the method of radio thermoluminescence, in which a deeply penetrating γ-quanta from 60Co radiation was used for activation of the bulk. A marked difference in a temperature position of the peaks on the glow curves of plasma-induced thermoluminescence and those of radiothermoluminescence correspoding to γ- and ß-transitions was found to depend on crystallisation conditions and molecular weight. Quasi-independent segmental mobility (ß-relaxation) in the near-surface nano-layers of UHMWPE reactor powder particles synthesized at low temperatures appeared to be unexpectedly unfreezed at the temperature higher than that in the bulk. It was supposed that this happend because of crystallization under the confinement conditions during low-temperature polymerization leads to formation of a specific surface structure.

Proton Modification of Ultra High Molecular Weight Polyethylene to Promote Crosslinking for Enhanced Chemical and Physical Properties

1995 ◽  
Vol 396 ◽  
Author(s):  
J.F. Wilson ◽  
J.R. Liu ◽  
F. Romero-Borja ◽  
W.K. Chu
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Surface Region ◽  
Low Doses ◽  
Carbonyl Groups ◽  
Hydrogen Annealing ◽  
Near Surface ◽  
Gel Permeation ◽  
Ultra High Molecular Weight

AbstractCrosslinking onset was investigated for ultra high molecular weight polyethylene(UHMW-PE) implanted with 2.6 MeV H+ ions at low doses from 6×1011-3×1013 ions/cm2. Crosslinking in the near surface region(20–40μm) was determined from gel permeation chromatography(GPC) of 1,2,4 trichlorobenzene sol fractions and increased with dose. Fourier transform infrared spectroscopy(FTIR) showed irradiation resulted in increased free radicals confirmed from increased carbonyl groups. Hydrogen annealing after ion implantation resulted in 38–49% decrease in FTIR peak associated with carbonyl.

Bonding of Ultra High Molecular Weight Polyethylene to Styrene-Butadiene Rubber

1993 ◽  
Vol 66 (1) ◽  
pp. 92-97 ◽  
Author(s):  
Gary R. Hamed ◽  
Hasan S. Dweik
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Average Molecular Weight ◽  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Molecular Weights ◽  
Order Of Magnitude ◽  
High Bond ◽  
Styrene Butadiene ◽  
Ultra High Molecular Weight

Abstract The adhesion between a sulfur-vulcanized SBR and polyethylenes (PE) of various molecular weights has been determined using a T-peel geometry. When the viscosity average molecular weight of the polyethylene exceeds about 700 k, bonding is sufficient to cause rubber tear during peeling. In contrast, with PE of Mv≈147k, joint strength is reduced by more than an order of magnitude and fracture proceeds between the SBR and PE. It is hypothesized that the high bond strength with the ultra high molecular weight polyethylene (UHMWPE) is due to the formation of entrapped tangles between chains of the two adherends. Consistent with this, SBR-UHMWPE bonds are not disrupted after extensive swelling in toluene.

Improved EOR Polymer Selection Using Field-Flow Fractionation

2021 ◽  
Author(s):  
Johannes Steindl ◽  
Rafael Eduardo Hincapie ◽  
Ante Borovina ◽  
Christoph Puls ◽  
Johann Badstöber ◽  
...  
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Molecular Weight Distribution ◽  
Weight Distribution ◽  
Field Flow Fractionation ◽  
Molecular Weights ◽  
Chemical Eor ◽  
Flow Fractionation ◽  
Polymer Retention ◽  
Ultra High Molecular Weight

Abstract Various polyacrylamide polymers have been successfully applied in chemical EOR projects. These polymers are characterised by high molecular weights (MW) to achieve high viscosifying power. The molecular weight distribution (MWD) of the polymers has a major impact on polymer properties and performance. Measuring the molecular weight distribution is challenging using conventional methods. Field-Flow Fractionation (FFF) enables the determination of the distribution to select and quality check various polymers. Polymers with high molar masses (> 1 MDa) are used for EOR to obtain highly viscous aqueous solutions. The MWD of the polymers is crucial for the solution characteristics. Conventional analysis of polymers is performed using either viscometry – which is able to determine the average MW but does not give information on MWD, or size-exclusion chromatography – which is restricted to molecular weights of < 20 MDa. FFF is based on the analytes flowing at different speeds in a channel dependent on their size and mass. This effect leads to separation, which is then used to determine the MWD. FFF allows to determine the MW and MWD of various ultra-high molecular weight polyacrylamides (HPAAMs). The FFF measurements showed, that despite similar MWs are claimed, substantial differences in MWD are observed. This technology offered the quantification the MWD of HPAAMs up to a MW of 5 GDa. Furthermore, gyration radii of the HPAAM molecules were determined. Selecting polymers on viscosifying power only is not addressing issues related to different MW and MWDs such as selective polymer retention and degradation of the high molar mass part of the distribution. The results were used to improve the polymer selection for chemical EOR projects. Overall, this work presents a new technique for analysis of ultra-high molecular weight EOR polymers, which enables the possibility to determine the full range of polymer MWD. This available information enhances the EOR polymer selection process addressing selective polymer retention and mechanical degradation in addition to the viscosifying power of polymers.

HIGHLY CROSSLINKED POLYETHYLENE: A COMPARATIVE STUDY BETWEEN TWO UHMWPES WITH DISTINCT MOLECULAR WEIGHT

2010 ◽  
Vol 10 (01) ◽  
pp. 95-111 ◽  
Author(s):  
DANIELA FERRONI ◽  
VIRGINIO QUAGLINI ◽  
PAOLO DUBINI
Keyword(s):  
Molecular Weight ◽  
Wear Resistance ◽  
Comparative Study ◽  
High Molecular Weight ◽  
End User ◽  
Wear Properties ◽  
Short Term ◽  
Molecular Weights ◽  
Radiation Induced ◽  
Ultra High Molecular Weight

In the recent years, radiation-induced highly crosslinked polyethylenes have been introduced in arthroplasties as an alternative to conventional ultra high molecular weight polyethylene (UHMWPE) for their superior wear resistance. In the present study, the influence of the molecular weight of the raw on end-user properties of highly crosslinked polyethylenes (HXLPE) is investigated by means of a comparative study between two resins with distinct molecular weights. The main outcomes indicate that the differences in mechanical and wear properties between the row materials disappear after crosslinking; nevertheless the resin with the highest molecular weight is likely to retain a better resistance to short-term oxidation.

Shock consolidation of Ni-Ti alloy powder

1986 ◽  
Vol 44 ◽  
pp. 430-431
Author(s):  
Naresh N. Thadhani ◽  
Thad Vreeland ◽  
Thomas J. Ahrens
Keyword(s):  
Alloy Powder ◽  
Amorphous Material ◽  
Ti Alloy ◽  
Two Phase ◽  
Near Surface ◽  
Optical Micrograph ◽  
Shock Compaction ◽  
Powder Particles ◽  
Ti Powder ◽  
Rapidly Solidified

A spherically-shaped, microcrystalline Ni-Ti alloy powder having fairly nonhomogeneous particle size distribution and chemical composition was consolidated with shock input energy of 316 kJ/kg. In the process of consolidation, shock energy is preferentially input at particle surfaces, resulting in melting of near-surface material and interparticle welding. The Ni-Ti powder particles were 2-60 μm in diameter (Fig. 1). About 30-40% of the powder particles were Ni-65wt% and balance were Ni-45wt%Ti (estimated by EMPA).Upon shock compaction, the two phase Ni-Ti powder particles were bonded together by the interparticle melt which rapidly solidified, usually to amorphous material. Fig. 2 is an optical micrograph (in plane of shock) of the consolidated Ni-Ti alloy powder, showing the particles with different etching contrast.

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.

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