Search results for "MACRO"

showing 10 items of 3471 documents

Recycling of dry and wet polyamide 6

2002

Recycling of polycondensation polymers can give rise to secondary materials with good mechanical properties only if a careful drying is carried out before the melt reprocessing operations. The presence of humidity provokes the hydrolytic chain scission of the macromolecules and the consequent decrease of molecular weight and properties. In this work, the drying step was substituted by the addition of an antioxidant that is able to protect the macromolecules because it is the autioxidant is more prone to hydrolysis, thus removing the water from the melt. The mechanical properties of polyamide 6 reprocessed more times in wet conditions and in the presence of this stabilizer are even better th…

chemistry.chemical_classificationCondensation polymerPolymers and PlasticsChain scissionHumidityGeneral ChemistryPolymerSurfaces Coatings and FilmsHydrolysisSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryChemical engineeringPolyamideMaterials Chemistryrestabilizatiob plastics polyamide recyclingOrganic chemistryMacromoleculeStabilizer (chemistry)Journal of Applied Polymer Science
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Synthesis of a New pH-Dependent Ligand: Conformational and Complexation Studies

2003

A new macrocyclic ligand, 3, which exhibits pH-induced conformational changes, has been prepared. This ligand consists of a crown ether derived from a trans-anti-trans 1,2,4,5-tetrasubstituted cyclohexane. Due to the stereochemistry of the substituents on the carbocyclic ring, two different low-energy conformations of the crown ether are possible. Ligand 3 has been studied in solution by 1H NMR spectroscopy at different values of pH and temperature, showing that the conformation of the crown ether, and thus its complexing ability, is strongly pH-dependent. The solid-state structure of the ligand has been determined by X-ray diffraction.

chemistry.chemical_classificationCrystallography1h nmr spectroscopychemistry.chemical_compoundchemistryCyclohexaneStereochemistryPh dependentGeneral ChemistryMacrocyclic ligandLigand (biochemistry)Ring (chemistry)Crown etherSupramolecular Chemistry
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Direct Visualization of Pyrrole Reactivity upon Confinement within a Cyclodextrin Metal–Organic Framework

2019

Metal–organic frameworks can be used as porous templates to exert control over polymerization reactions. Shown here are the possibilities offered by these crystalline, porous nanoreactors to capture highly-reactive intermediates for a better understanding of the mechanism of polymerization reactions. By using a cyclodextrin framework the polymerization of pyrrole is restricted, capturing the formation of terpyrrole cationic intermediates. Single-crystal X-ray diffraction is used to provide definite information on the supramolecular interactions that induce the formation and stabilization of a conductive array of cationic complexes.

chemistry.chemical_classificationCyclodextrin010405 organic chemistryChemistrytechnology industry and agricultureSupramolecular chemistryCationic polymerizationGeneral Medicinemacromolecular substancesGeneral ChemistryNanoreactor010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical scienceschemistry.chemical_compoundPolymerizationNon-covalent interactionsMetal-organic frameworkPyrroleAngewandte Chemie International Edition
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Significance of various enzymes in the control of reactive metabolites

1987

Most chemical carcinogens are relatively inert and need metabolic activation to the ultimately carcinogenic species. The concentration of such species is controlled by several different enzymes. Especially well studied is the important group of enzymes responsible for the control of reactive epoxides. Many natural, as well as man-made foreign compounds, including pharmaceuticals, possess olefinic or aromatic double bonds. Such compounds can be transformed to epoxides by microsomal monooxygenases present in many mammalian organs. By virtue of their electrophilic reactivity, such epoxides may spontaneously react with nucleophilic centres in the cell and thus covalently bind to DNA, RNA and pr…

chemistry.chemical_classificationDNA repairHealth Toxicology and MutagenesisGeneral MedicineBiologyMonooxygenaseToxicologyEnzymeschemistry.chemical_compoundEnzymeBiochemistrychemistryEpoxide HydrolasesCarcinogensAnimalsEpoxy CompoundsHumansEpoxide hydrolaseCarcinogenDNAMacromoleculeArchives of Toxicology
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Formation rates and protonation constants of azo dyes in a sodium dodecylsulphate micellar solution.

1991

The effects of a sodium dodecylsulphate micellar solution on the coupling rates of several diazotizated arylamines with N-(1-naphthyl)-ethylenediamine and the shifts in the protonation constants of the corresponding azo dyes are quantitatively studied. Aniline, o-, m- and p-aminobenzoic acids, ethyl p-aminobenzoate and several sulphadrugs are used, and the relationships among the intensity of the effects and the molecular structure of the diazonium ions and the dyes are discussed. A single simplified procedure for the determination of all the substances at pH = 1.3 +/- 0.3, where coupling is quickly completed to directly produce the protonated form of the dyes, is established and applied to…

chemistry.chemical_classificationDiazonium CompoundsSodiumInorganic chemistrychemistry.chemical_elementProtonationmacromolecular substancesDosage formAnalytical ChemistryIonchemistry.chemical_compoundAnilinechemistryMoleculeProtonation constantTalanta
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A continuous reaction system to investigate dispersion polymerization of vinyl monomers in supercritical carbon dioxide

2006

A laboratory-scale continuous reaction system using a stirred tank reac- tor was assembled in our laboratory to study the dispersion polymerization of vinyl monomers in supercritical carbon dioxide (scCO2). The apparatus was equipped with a suitable downstream separation section to collect solid particles entrained in the effluent stream from the reactor, whose monomer concentration could be measured online with a gas chromatograph. The dispersion polymerization of methyl methacry- late in scCO2 was selected as a model process to be investigated in the apparatus. The experiments were performed at 65 8C and 25 MPa with 2,2 0 -azobisisobutyroni- trile as the initiator and a reactive polysilox…

chemistry.chemical_classificationDispersion polymerizationSupercritical carbon dioxidePolymers and PlasticsBulk polymerizationOrganic ChemistryRadical polymerizationmacromonomerPolymerSettore ING-IND/27 - Chimica Industriale E TecnologicaMacromonomerradical polymerizationkinetics (polym.)chemistry.chemical_compoundMonomerchemistryPolymerizationChemical engineeringpolysiloxanesupercritical carbon dioxidePolymer chemistryMaterials Chemistrydispersion
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Interaction Mechanisms between guaiacols and lignin: the conjugated double bond makes the difference.

2011

Lignin is considered to be responsible for a selective sorption of phenolic compounds on wood. In order to investigate the mechanisms involved, two similar guaiacol compounds--only differing by the nature of the para side chain--were adsorbed on oak wood extracted lignin. Vapor sorption-desorption isotherms indicated that about 3.5 wt % of 4-vinylguaiacol is adsorbed near saturation whereas it is only 0.8% for 4-ethylguaiacol. For both compounds, the isotherms displayed a hysteresis though significantly greater for 4-vinylguaiacol. Analyses of the hydroxyl stretching region of FTIR spectra of the lignin/4-ethylguaiacol and lignin/4-vinylguaiacol complexes indicated that physisorption via hy…

chemistry.chemical_classificationDouble bondHydrogen bondChemistrytechnology industry and agriculturemacromolecular substancesSurfaces and InterfacesConjugated systemCondensed Matter Physicscomplex mixturesNMR spectra databasechemistry.chemical_compoundPhysisorptionDesorptionElectrochemistryLigninOrganic chemistryGeneral Materials ScienceGuaiacolSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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COMPOSITION AND QUALITY OF FRESHWATER LAKE SEDIMENTS (BALVU AND PĒRKONU LAKES)

2019

Water quality, watershed basin and urbanization are key factors from the perspective of freshwater management; however, actual depth of waterbodies is often an overlooked element. Actual depth represents the overall depth of lake bed and depth of sediments. Some cases have been reported, where with increase of average depth of lake , it is possible to expect improvements of water quality when sediments are removed. If lakes are eutrophic, shallow, overgrown with macrophytes and contain high concentrations of biogenic elements water and lake ecosystem quality can be endangered. Removal of sediments can be an expensive procedure and also depends on the composition, structure, local conditions…

chemistry.chemical_classificationDredgingHydrologyeutrophication; dredging; lake sediments; pollutionchemistryLake ecosystemEnvironmental scienceOrganic matterSTREAMSWater qualitySedimentationEutrophicationMacrophyteENVIRONMENT. TECHNOLOGIES. RESOURCES. Proceedings of the International Scientific and Practical Conference
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Chemical conjugation of dexamethasone to a polyaspartamide and in vitro evaluation studies

2004

Two macromolecular conjugates of dexamethasone containing different drug amounts were synthesized using PHEA as the polymeric carrier and a succinic group as spacer. The content of linked drug was equal to 25.3% w/w (conjugate A) and 12.7% w/w (conjugate B). Both polymeric conjugates, unlike the free drug, were water-soluble and the amount of unlinked drug was evaluated to be approximately about 0.01% w/w. Both conjugates were relatively stable in vitro at pH 7.4 whereas in the presence of esterase only the conjugate B was able to release drug under the used experimental conditions. This dissimilar behavior has been attributed to the distinct macromolecular conformations assumed in aqueous …

chemistry.chemical_classificationDrugStereochemistrymedia_common.quotation_subjectPharmaceutical ScienceProdrugEsteraseCombinatorial chemistryDexamethasoneIn vitroPolyaspartamideHydrolysisEnzymechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug-polymer conjugatesMacromoleculemedia_commonConjugateJournal of Drug Delivery Science and Technology
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Competition between degradation and chain extension during processing of reclaimed poly(ethylene terephthalate)

1998

During processing of poly(ethylene terephthalate) (PET) hydrolytic chain scission, induced by the presence of small amounts of water, is the main cause of degradation. During repeated reprocessing chain scission can also occur because of the presence of other polymeric contaminants like PVC. In order to avoid or to limit hydrolytic chain cleavage adequate drying of PET before melt processing is necessary. Of course this practice is even more recommended when repeated processing steps are used, as for PET recycling. The behavior of recycling PET obtained from post-consumer water bottles when treated in a melt mixer under different conditions has been investigated in order to better understan…

chemistry.chemical_classificationEthyleneMaterials sciencePolymers and PlasticsChain scissionNitrogen atmospheremacromolecular substancesPolymerCondensed Matter Physicschemistry.chemical_compoundHydrolysischemistryChemical engineeringChain (algebraic topology)Mechanics of MaterialsPolymer chemistryMaterials ChemistryDegradation (geology)Poly ethylene
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