Glass transition temperature of allyl methacrylate-n-butyl acrylate gradient copolymers in dependence on chemical composition and molecular weight

2007 ◽  
Vol 45 (14) ◽  
pp. 1845-1855 ◽  
Author(s):  
Rodrigo París ◽  
José Luis De la Fuente
2011 ◽  
Vol 183-185 ◽  
pp. 1938-1941
Author(s):  
Jiu Yin Pang ◽  
Chuan Sun ◽  
Shi Cheng Zhang ◽  
Zhen Xing

Miniemulsion was prepared by means of different ratio of butyl acrylate with vinyl acetate emulsion pressure sensitive adhesive excellent performance. Focused on acrylic acid and vinyl acetate copolymers of different proportions of the glass transition temperature, molecular weight and molecular weight distribution of micro-factors, and build the macroscopic properties of the copolymer glass transition temperature and molecular weight between contacts. The use of APS as initiator under the conditions of the experiment found that with the increase of acrylic, PVC-floor, 180 peel strength composite materials decreased. While the molecular weight of butyl acrylate with the increase of the amount did not change significantly, the initial viscosity of the polymer and 180 º peel strength is improved, but the adhesive holding down quickly.


1998 ◽  
Vol 10 (3) ◽  
pp. 273-283 ◽  
Author(s):  
J W Connell ◽  
J G Smith ◽  
P M Hergenrother

As part of a programme to develop high-performance/high-temperature structural resins for aeronautical applications, imide oligomers containing pendent and terminal phenylethynyl groups were prepared, characterized and the cured resins evaluated as composite matrices. The oligomers were prepared at a calculated number-average molecular weight of 5000 g mol−1 and contained 15–20 mol% pendent phenylethynyl groups. In previous work, an oligomer containing pendent and terminal phenylethynyl groups exhibited a high glass transition temperature (∼313 °C), and laminates therefrom exhibited high compressive properties, but processability, fracture toughness, microcrack resistance and damage tolerance were less than desired. In an attempt to improve these deficiencies, modifications in the oligomeric backbone involving the incorporation of 1,3-bis(3-aminophenoxy)benzene were investigated as a means of improving processability and toughness without detracting from the high glass transition temperature and high compressive properties. The amide acid oligomeric solutions were prepared in N-methyl-2-pyrrolidinone and were subsequently processed into imide powder, thin films, adhesive tape and carbon fibre prepreg. Neat resin plaques were fabricated from imide powder by compression moulding. The maximum processing pressure was 1.4 MPa and the cure temperature ranged from 350 to 371 °C for 1 h for the mouldings, adhesives, films and composites. The properties of the 1,3-bis(3-aminophenoxy)benzene modified cured imide oligomers containing pendent and terminal phenylethynyl groups are compared with those of previously prepared oligomers containing pendent and terminal phenylethynyl groups of similar composition and molecular weight.


2018 ◽  
Vol 18 (9) ◽  
pp. 6331-6351 ◽  
Author(s):  
Wing-Sy Wong DeRieux ◽  
Ying Li ◽  
Peng Lin ◽  
Julia Laskin ◽  
Alexander Laskin ◽  
...  

Abstract. Secondary organic aerosol (SOA) accounts for a large fraction of submicron particles in the atmosphere. SOA can occur in amorphous solid or semi-solid phase states depending on chemical composition, relative humidity (RH), and temperature. The phase transition between amorphous solid and semi-solid states occurs at the glass transition temperature (Tg). We have recently developed a method to estimate Tg of pure compounds containing carbon, hydrogen, and oxygen atoms (CHO compounds) with molar mass less than 450 g mol−1 based on their molar mass and atomic O : C ratio. In this study, we refine and extend this method for CH and CHO compounds with molar mass up to ∼ 1100 g mol−1 using the number of carbon, hydrogen, and oxygen atoms. We predict viscosity from the Tg-scaled Arrhenius plot of fragility (viscosity vs. Tg∕T) as a function of the fragility parameter D. We compiled D values of organic compounds from the literature and found that D approaches a lower limit of ∼ 10 (±1.7) as the molar mass increases. We estimated the viscosity of α-pinene and isoprene SOA as a function of RH by accounting for the hygroscopic growth of SOA and applying the Gordon–Taylor mixing rule, reproducing previously published experimental measurements very well. Sensitivity studies were conducted to evaluate impacts of Tg, D, the hygroscopicity parameter (κ), and the Gordon–Taylor constant on viscosity predictions. The viscosity of toluene SOA was predicted using the elemental composition obtained by high-resolution mass spectrometry (HRMS), resulting in a good agreement with the measured viscosity. We also estimated the viscosity of biomass burning particles using the chemical composition measured by HRMS with two different ionization techniques: electrospray ionization (ESI) and atmospheric pressure photoionization (APPI). Due to differences in detected organic compounds and signal intensity, predicted viscosities at low RH based on ESI and APPI measurements differ by 2–5 orders of magnitude. Complementary measurements of viscosity and chemical composition are desired to further constrain RH-dependent viscosity in future studies.


2020 ◽  
Vol 869 ◽  
pp. 190-195
Author(s):  
Yuri Mikhailov ◽  
Ludmila Romanova ◽  
Anna Darovskikh ◽  
Nilson Garifullin

Some properties (enthalpy of formation, glass transition temperature and rheological parameters) of hyperbranched polyglycidol derivatives containing nitrate and azide functional groups were investigated. The dependence of the found properties on the molecular weight, composition and structure of the investigated substances was determined.


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