Brief introduction of 4,5-Difluorophthalic Anhydride

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High temperature resins containing phenylethynyl groups that are processable by transfer molding have been prepared. These phenylethynyl containing oligomers were prepared from aromatic diamines containing phenylethynyl groups and various ratios of phthalic anhydride and 4-phenylethynlphthalic anhydride in glacial acetic acid to form a mixture of imide compounds in one step. This synthetic approach is advantageous since the products are a mixture of compounds and consequently exhibit a relatively low melting temperature. In addition, these materials exhibit low melt viscosities which are stable for several hours at 210-275 C., and since the thermal reaction of the phenylethynyl group does not occur to any appreciable extent at temperatures below 300 C., these materials have a broad processing window. Upon thermal cure at ?300-350 C., the phenylethynyl groups react to provide a crosslinked resin system. These new materials exhibit excellent properties and are potentially useful as adhesives, coatings, films, moldings and composite matrices.

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Discovery of 4,5-Difluorophthalic Anhydride

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Quality Control of 4,5-Difluorophthalic Anhydride, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 18959-30-3, Name is 4,5-Difluorophthalic Anhydride, molecular formula is C8H2F2O3

A reactive diluent (ODA-PEPA) and a flexible phenylethynyl-terminated imide oligomer (PEI-PEPA) were designed and synthesized based on the 2,3,3?,4?-diphenyl ether tetracarboxylic acid dianhydride (a-ODPA), 3,4?-oxydianiline (3,4?-ODA), and 4-phenylethynylphthalic anhydride (PEPA). Solution blended systems with the addition of 5, 10, and 15 wt% ODA-PEPA to PEI-PEPA oligomer and their cured resin systems were prepared. Results showed that ODA-PEPA is semi-crystalline in nature. The Tg values of cured resins were improved from 273 C to 280 C by the addition of ODA-PEPA, due to the higher crosslink densities. In addition, rheological properties of blends showed lower melt viscosity and wider processing window, revealing improved melt processabilities for potential application in making advanced composites. The isothermal viscosity in 280 C of PEI-PEPA containing 15 wt% ODA-PEPA reactive diluent decreased by two thirds, due to the low molecular weight of ODA-PEPA. The cured blends demonstrated high thermal stability and heat resistance. 5 wt% thermal decomposition temperatures (Td5) of the cured blends were above 549 C and 547 C in N2 and air atmosphere, respectively. The char yield reported at 800 C in N2 atmosphere increased from 58.8% to 63.7 % with the addition of ODAPEPA. Meanwhile, the cured polyimides blends possessed good bond strength (> 9.3 MPa).

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New explortion of 4,5-Difluorophthalic Anhydride

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18959-30-3, Name is 4,5-Difluorophthalic Anhydride, belongs to benzofurans compound, is a common compound. HPLC of Formula: C8H2F2O3In an article, once mentioned the new application about 18959-30-3.

To investigate the effect of reactive end-capping groups on film-forming quality and processability, a series of molecular weight-controlled aromatic poly(amic acid) (PAA) resins functionalized with phenylethynyl end groups were prepared via the polycondensation of 3,3?,4,4?-biphenyltetracarboxylic dianhydride (BPDA), para-phenylenediamine (PDA), and 4-phenylethynyl phthalic anhydride (PEPA) served as molecular-weight-controlling and reactive end capping agent. The PAA resins with relatively high concentrations endow enhanced wetting/spreading ability to form PAA gel films by solution-cast method which were thermally converted to the fully-cured polyimide (PI) films. The mechanical and thermal properties of PI films were investigated as a function of PAA molecular weights (Mn) and thermal-curing parameters. Mechanical property, dimensional stability and heat resistance of the fully-cured PI films with PAA Mn > 20 ×103 g mol?1 are found to be better than that of their unreactive phthalic end-capped counterparts. The covalent incorporation of chain-extension structures in the backbones, induced by thermal curing of phenylethynyl groups, might facilitate yielding a higher degree of polymer chain order and consequently improved resistance strength and elongation at break to tensile plastic deformation.

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Electric Literature of 18959-30-3, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Article in Press, and a compound is mentioned, 18959-30-3, 4,5-Difluorophthalic Anhydride, introducing its new discovery.

The thermal oxidative stability of a 4-phenylethynyl phthalic anhydride (PEPA) endcapped polyimide (PI) was investigated. A surface reaction layer formed due to oxidization during thermal aging and grew in thickness with increasing aging time. Analysis of the surface layer revealed a partial loss of aromatic ring, ether linkage, and imide linkage in the aged polymer. The partial loss of the imide linkage and ether linkage in the surface layer was corroborated by the observed release of carbon monoxide and carbon dioxide reaction products. The oxidized layer exhibited discoloration and an increase in glass transition temperature. The surface discoloration was attributed to the formation of the conjugated unsaturated or aromatic carbonyl groups and/or the charge transfer complex. Interior regions of the oxidized samples were largely unaffected, except for a more compact molecular configuration. Compared with aging at high temperatures (288C, 316C), aging at 204C produced similar chemical changes in the cured polymer, albeit with a low degradation rate. The oxidative stability of the imide polymer surpassed that of conventional nadic-endcapped PIs due to the greater intrinsic thermal stability of the PEPA endcap. The unusual oxidative stability of the PI, combined with superior mechanical properties, warrant consideration as a composite matrix for future applications in high-temperature service conditions.

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Electric Literature of 18959-30-3, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 18959-30-3, molcular formula is C8H2F2O3, introducing its new discovery.

A previously developed carbon fibre-reinforced addition-type polyimide composite material was exposed to temperatures of 240, 270 and 300 C in air for 3000 h to study its long-term stability in terms of its compressive strength. The in-plane shear modulus, compressive failure mode and transverse crack density were also evaluated to determine whether a degradation process induces a decrease in the compressive strength of a high-temperature polymer matrix composite having a laminated configuration of [90/0]4s. The carbon fibre-reinforced polyimide composite exhibited excellent thermal stability in terms of its compressive strength after being subjected to ageing at 240 C for 3000 h and at 270 C for 2000 h, with degradation becoming significant at 300 C. The compressive strength decreased only when the surface degradation caused the 90 plies sandwiching the 0 plies to degrade severely.

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The effects of thermal cycling on a polymerized monomeric reactant (PMR) type polyimide (TriA X) reinforced with carbon fibers were investigated. Composite specimens were subjected to 2000 thermal cycles between ?54C and 232C. At 400-cycle intervals, laminates were inspected for microcracks, and glass transition temperature (Tg) and short-beam shear (SBS) strength were measured. The composites did not exhibit microcracks after thermal cycling, although after 2000 thermal cycles, mechanical properties of the matrix declined slightly. The matrix degradation decreased the resistance to microcracking upon further loading. No effects of thermal oxidative aging were observed from thermal cycling, and thermally driven fatigue and creep were identified as the primary and secondary factors inducing mechanical degradation of the matrix. Tg of the composites exhibited no change after 2000 cycles, while the SBS strength decreased slightly (3?9%). The results highlight the potential for use of TriA X composites as long-term structural components in high-temperature service environments.

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Related Products of 18959-30-3, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 18959-30-3, Name is 4,5-Difluorophthalic Anhydride,introducing its new discovery.

The previously developed TriA-X polyimide resin, consisting of pyromellitic dianhydride/2-phenyl-4,4?-diaminodiphenyl ether; 9,9-bis(4-aminophenyl)fluorene/4-phenylethynylphthalic anhydride (PEPA), was exposed for 3000 h to air at 180, 240, and 270C or a vacuum environment at 270C, in order to study its long-term thermal stability. The weight loss and dimensional changes were measured. Elemental analysis was also conducted in order to estimate the TriA-X degradation process. The TriA-X exhibited excellent thermal stability at 180C and a very small degree of degradation at 240C, with the degradation becoming significant at 270C. The latter was primarily dominated by the oxidation of a chain-extension moiety formed by the cure reaction of the end-cap PEPA.

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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 18959-30-3, name is 4,5-Difluorophthalic Anhydride, introducing its new discovery. COA of Formula: C8H2F2O3

A series of oligomers based on the mixture of thioetherdiphthalic anhydride isomers and 4,4?-oxydianiline with 4-phenylethynylphthalic anhydride as reactive endcapping reagent were prepared. The calculated molecular weights were in the range of 1150-5070 g mol-1 with different degrees of polymerization (n = 1, 3, 5, 7, and 9). The effect of molecular weight of the aromatic oligomers on their processability and solubility as well as the thermal and mechanical properties of the thermal-cured polyimides (PIs) was systematically investigated. The typical oligomer (Oligo-1) could be melted at temperatures of 289-334C to yield stable molten fluid with melt viscosity below 1.0 Pa s. The melt viscosity of the oligomers increased with the increasing molecular weight. After thermally curing at 370C, the thermoset PIs exhibited good thermal properties. The glass transition temperatures of oligomers measured by differential scanning calorimetry were in the range of 286-326C, and the temperature of 5% weight loss was higher than 524C. The cured films also showed good mechanical properties with tensile strength above 72 MPa and modulus more than 2.5 GPa.

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Novel highly soluble phenylethynyl-endcapped oligoimides with different calculated molecular weights were prepared by using mellophanic dianhydride and bis(4-amino-2-trifluoromethylphenyl)ether in the presence of 4-phenylethynyl phthalic anhydride as the reactive endcapping agent. The effect of molecular weights of the aromatic oligoimides on their solubility and processability as well as the thermal and mechanical properties of the thermal-cured polyimides was fully investigated. This kind of phenylethynyl-terminated imides exhibited excellent comprehensive properties. Most importantly, a big progress has been made in the solubility of the oligoimides in this paper. Most of the oligoimides showed excellent solubility (more than 33 wt%) even in acetone, which was reported for the first time. And oligoimides with appropriate molecular weights also showed very good processability with minimum melt viscosities no higher than 120 Pa·s by the rheological study. After thermally curing at 370C for 1 hour, the cured flexible films showed very high glass transition temperatures up to 392C by dynamic mechanical analysis, and the temperature of 5% weight loss was higher than 500C in both air and N2 atmosphere by thermogravimetric analysis. The cured films also exhibited very good toughness with elongation up to 9%.

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The Absolute Best Science Experiment for 4,5-Difluorophthalic Anhydride

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Novel imide oligomers (calculated molecular weights: 1250-5000 g mol1) based on the mixture of thioetherdiphthalic anhydride isomers (m-TDPA) with 2-phenyl-4,4?-diaminodiphenyl ether (p-ODA) in the presence of 4-phenylethynylphthalic anhydride (PEPA) as reactive endcapping agent were prepared. Then pyromellitic dianhydride (PMDA) was introduced to the polymerization of m-TDPA/p-ODA (mole m -TDPA:molePMDA = 1:1). The effect of molecular weights and polymer chemical structures of the aromatic oligomers on their processability and solubility as well as the thermal and mechanical properties of the thermal-cured polyimides (PIs) was systematically investigated. All the oligomers showed good solubility (more than 30 wt%) in N-methyl-2-pyrrolidone and very low melt viscosities. The minimum melt viscosities of Oligo-5 was 61.5 Pa s at 321C. The melt viscosity of the oligomers increased with the increase of molecular weight. After thermally curing at 370C for 1 h, the thermoset PIs exhibited good thermal properties. The glass transition temperatures of oligomers measured by differential scanning calorimetry were in the range of 264-337C, and the temperature of 5% weight loss was higher than 505C. The cured films also demonstrated good mechanical properties with tensile strength and modulus greater than 52 MPa and 2.9 GPa, respectively.

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