Search results for "POLYMERIZATION"

showing 10 items of 1689 documents

Organometallic VCl4-based catalyst supported on MgCl2(THF)2 for ethylene polymerization

1997

A Ziegler-Natta catalyst was obtained by milling VCl4 with the magnesium support in the from of the MgCl2(THF)2 complex, followed by activation with an organoaluminum compound. This catalyst was employed in low-pressure polymerization of ethylene. The system was found to offer a very high activity and to polymerize ethylene at a rate of a few hundred kg PE/(g Vh) with the resulting molecular weight of the product very high. The kinetic investgation of the polymerization process revealed over 80 % of the transition metal atoms to be involved in the forming catalytic active sites, undergoing virtually no deactivation over the period of time studied.

polymerization of ethyleneactivityZiegler-Natta type catalystdeactivationPolimery
researchProduct

Weryfikacja kinetycznego modelu polimeryzacji etylenu wobec metaloorganicznych katalizatorów wanadowych na nośniku magnezowym

1998

The kinetic studies are reviewed on low-pressure polymerization of ethylene over two types of organovanadium catalysts, viz., MgCl 2(THF) 2/VCl 4/Et 2AlCl and MgCl 2(THF) 2VOCl 3Et 2AlCl, each deposited on a magnesium carrier. The polymerization rate was found to be directly related to the catalyst and monomer concentrations (Figs. 2 and 3), unless when the access of the monomer to the reactive V-C bond is restricted by diffusion. Polymer chain termination step was found to result from the reaction of the transfer onto the monomer and to be associated with the regeneration of the active site on which a new macromolecule can be formed. A kinetic model was developed for the ethylene polymeriz…

polymerization of ethylenemechanism of termination reactionorganovanadium catalysts on carrierskinetic model of polymerizationPolimery
researchProduct

Synthesis of oxide-supported vanadium catalysts and their activity in ethylene polymerization

1999

The activity of oxide-supported vanadium-based catalyst systems (VOCl 3/Et 2AlCl) in low-pressure ethylene polymerization and the properties of the resulting polyethylenes were studied in relation to the type and mode of modification of the oxide support. Alumina, silica and an un"conventional silica-type material prepared by the sol-gel process were used as supports. Results are compared with those obtained earlier with a catalyst supported on MgCl 2(THF) 2. Of the oxides studied, the silica-type sol-gel material dehydrated and subsequently modified with Et 2AlCl proved to be the best carrier for a vanadium catalyst. The polyethylene prepared by using this catalyst support was found to exh…

polymerization of ethylenevanadium catalystsol-gel processsol-gel silica-type carrieroxide supportPolimery
researchProduct

Polysarcosine-Based Lipids: From Lipopolypeptoid Micelles to Stealth-Like Lipids in Langmuir Blodgett Monolayers.

2016

Amphiphiles and, in particular, PEGylated lipids or alkyl ethers represent an important class of non-ionic surfactants and have become key ingredients for long-circulating (“stealth”) liposomes. While poly-(ethylene glycol) (PEG) can be considered the gold standard for stealth-like materials, it is known to be neither a bio-based nor biodegradable material. In contrast to PEG, polysarcosine (PSar) is based on the endogenous amino acid sarcosine (N-methylated glycine), but has also demonstrated stealth-like properties in vitro, as well as in vivo. In this respect, we report on the synthesis and characterization of polysarcosine based lipids with C14 and C18 hydrocarbon chains and their end g…

polysarcosine; polypeptoids; surfactants; lipids; NCA polymerization; PSarcosinylated lipidsPolymers and PlasticsDispersity02 engineering and technologypolysarcosineDegree of polymerization010402 general chemistry01 natural sciencesMicelleRing-opening polymerizationLangmuir–Blodgett filmArticlesurfactantslipidslcsh:QD241-441PSarcosinylated lipidslcsh:Organic chemistryMonolayerPolymer chemistryOrganic chemistrypolypeptoidsNCA polymerizationChemistryGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesEnd-groupCritical micelle concentrationlipids (amino acids peptides and proteins)0210 nano-technologyPolymers
researchProduct

Comparison of imidazolium and pyridinium ionic liquids as the media for biphasic ethylene polymerization in the presence of titanocene catalyst

2009

Chloroglinianowe ciecze jonowe z kationem 1-n-oktylo-3-metylopirydyniowym [C8-β-mpy]+[AlCl4]- lub 1-n-oktylo-4-metylopirydyniowym [C8-γ-mpy]+[AlCl4]- zastosowano jako jedną z faz w dwufazowej polimeryzacji etylenu w układzie ciecz jonowa/heksan, prowadzonej wobec katalizatora tytanocenowego (Cp2TiCl2) aktywowanego AlEtCl2. Wydajności polimeryzacji i właściwości polimerów otrzymanych z udziałem wymienionych cieczy jonowych porównano z odpowiednimi wielkościami uzyskanymi wcześniej przy udziale cieczy imidazoliowej ([C8-mim]+ [AlCl4]-) (tabele 1 i 2). Stwierdzono, że wprowadzenie do układu pirydyniowych zamiast imidazoliowych cieczy jonowych skutkuje wzrostem całkowitej wydajności procesu, wi…

proces dwufazowyionic liquidsbiphasic processkatalizator metalocenowypolimeryzacja etylenupolyethylene propertiesciecze jonowemetallocene catalystethylene polymerizationwłaściwości polietylenuPolimery
researchProduct

Progression of Diiminopyridines: From Single Application to Catalytic Versatility

2015

Diiminopyridyl metal complexes, first characterized several decades ago, found practical application in 1998 when they were used as precatalysts in coordinative ethylene polymerization. This discovery contributed to the so-called postmetallocene revolution and triggered the large-scale experimental and theoretical research aimed at understanding diversified diiminopyridine chemistry. The results of this quest, some of which were intriguing and difficult to anticipate, are discussed and summarized in the current Review.

redox reactiontransition metal complexChemistrySingle applicationTheoretical researchNanotechnologyGeneral ChemistryCatalysisdiiminopyridinechemistry.chemical_compoundaluminum alkylEthylene polymerizationcooperative effectsOrganic chemistryOlefin polymerizationAluminum alkylolefin polymerizationDiiminopyridineACS Catalysis
researchProduct

Self-assembly of square planar rhodium carbonyl complexes with 4,4-disubstituted-2,2′-bipyridine ligands

2020

The impact of non-covalent interactions and reaction conditions on formation and self-assembly of ionic pairs of Rh complexes with 4,4’-disubstituted bipyridine ligands ([Rh(L1)(CO)2][Rh(CO)2Cl2])n (1), [Rh(L1)2Cl2][Rh(CO)2Cl2] (2), ([Rh(L1)(CO)2][Rh(CO)2Cl2][Rh(L1)(CO)2]n([Rh(CO)2(Cl)2])n) (3), ([Rh(L2)CO2] [Rh(CO)2Cl2])n∙EtOH (4), ([Rh(L2)(CO)2])n ([Rh(CO)2Cl2])n (5) (L1 = 4,4’-dimethyl-2,2’-bipyridine, L2 = 4,4’-diamine-2,2’-bipyridine) have been studied. Packing of square planar Rh complexes favor formation of one-dimensional chains. In structure 1, the polymeric chain is formed by the alternating cationic [Rh(L1)(CO)2]+ and the anionic [Rh(CO)2Cl2]- units leading to a neutral pseudo li…

reductive carbonylationchemistry.chemical_elementIonic bonding02 engineering and technology010402 general chemistry01 natural sciences22'-BipyridineRhodiumchemistry.chemical_compoundBipyridineGeneral Materials Sciencemetallophilicitychemistry.chemical_classificationLigandHydrogen bondCationic polymerizationcarbonylGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesCrystallographybipyridinechemistryrhodiumCounterion0210 nano-technologySolid State Sciences
researchProduct

The Effect of Mechanocatalytic Pretreatment on the Structure and Depolymerization of Willow

2020

In this study, the effect of a mechanocatalytic pretreatment on the structure of willow and sugar release from pretreated willow was explored. In the mechanocatalytic approach, the pretreatment consists of solvent-free impregnation with sulfuric acid and a mechanical treatment with ball milling. Willow sawdust and pretreated samples were analyzed with field emission scanning electron microscope and X-ray diffraction. The products in the sugar solution were determined as the total reducing sugars with the 3,5-dinitrosalicylic acid method and monosaccharides with capillary electrophoresis. According to the results, milling increased the sugar production, depending on the sulfuric acid load. T…

rikkihappo020209 energyselluloosaWillow sawdustpajut02 engineering and technology010501 environmental sciencesXyloseesikäsittelylcsh:Chemical technologycomplex mixtures01 natural sciencesCatalysisHydrolysatepolymerointilcsh:ChemistryBall millingchemistry.chemical_compoundlignocellulose0202 electrical engineering electronic engineering information engineeringmechanocatalytic pretreatmentMonosaccharidelcsh:TP1-1185Physical and Theoretical ChemistrySugarBall mill0105 earth and related environmental scienceschemistry.chemical_classificationDepolymerizationSulfuric acidsulfuric aciddigestive oral and skin physiologytechnology industry and agriculturefood and beveragesSulfuric acidwillow sawdustlcsh:QD1-999chemistryvisual_artvisual_art.visual_art_mediumball millingSawdustLignocelluloseMechanocatalytic pretreatmentNuclear chemistryCatalysts
researchProduct

Metal salen complexes as ethylene polymerization catalysts - effect of catalytic system composition on its activity and properties of polymerization …

2008

Zsyntetyzowano i zastosowano [po aktywacji metyloaluminoksanem (MAO) lub Et2AlCl] w charakterze katalizatorów niskociśnieniowej polimeryzacji etylenu serię salenowych kompleksów metali przejściowych różniących się rodzajem atomu centralnego (M=Ti, Zr lub V) i budową chemiczną ligandu (schemat A). Stwierdzono, że salenowe kompleksy cyrkonu są aktywne w polimeryzacji jedynie wówczas, gdy aktywator stanowi MAO, natomiast kompleksy tytanu i wanadu są aktywniejsze w przypadku gdy kokatalizatorem jest typowy związek glinoorganiczny - dietylochloroglin. Aktywność kompleksów w układzie z Et2AlCl zmienia się w szeregu V>Ti>>Zr?0, podczas gdy w odniesieniu do kompleksów aktywowanych MAO maleje ona w …

salenowe kompleksy metalipolyethyleneaktywnośćoligomerypolymerizationactivitysalen complexes of metalspost-metallocene catalystspolietylenoligomerskatalizatory postmetalocenowepolimeryzacjaPolimery
researchProduct

Extraordinary Performance of Carbon‐Coated Anatase TiO 2 as Sodium‐Ion Anode

2015

The synthesis of in situ polymer‐functionalized anatase TiO2 particles using an anchoring block copolymer with hydroxamate as coordinating species is reported, which yields nanoparticles (≈11 nm) in multigram scale. Thermal annealing converts the polymer brushes into a uniform and homogeneous carbon coating as proven by high resolution transmission electron microscopy and Raman spectroscopy. The strong impact of particle size as well as carbon coating on the electrochemical performance of anatase TiO2 is demonstrated. Downsizing the particles leads to higher reversible uptake/release of sodium cations per formula unit TiO2 (e.g., 0.72 eq. Na+ (11 nm) vs only 0.56 eq. Na+ (40 nm)) while the …

sodium‐ion batteriesAnataseMaterials scienceInorganic chemistryNanoparticle02 engineering and technology010402 general chemistryElectrochemistry7. Clean energy01 natural sciencessymbols.namesakeGeneral Materials ScienceHigh-resolution transmission electron microscopyRAFT polymerizationFull PaperRenewable Energy Sustainability and the EnvironmentFull Papers021001 nanoscience & nanotechnology0104 chemical sciencesAnodeanatase TiO2carbon coatingChemical engineeringsymbolsnanoparticlesParticle size0210 nano-technologyRaman spectroscopyFaraday efficiencyAdvanced Energy Materials
researchProduct