Rigid Polyurethane Foam (rigid + polyurethane_foam)

Distribution by Scientific Domains


Selected Abstracts


Oxypropylation of Lignins and Preparation of Rigid Polyurethane Foams from the Ensuing Polyols

MACROMOLECULAR MATERIALS & ENGINEERING, Issue 10 2005
Hamid Nadji
Abstract Summary: Different lignins were converted into polyols by a chain extension reaction with propylene oxide (PO). Thus, soda lignin from Alfa (Stipa tenacissima) (SL), organosolv lignin from hardwoods (OL), kraft lignin (KL) from softwood and oxidized organosolv lignin (OOL) were oxypropylated in a batch reactor at 180,°C in the presence of KOH as catalyst. The ensuing polyols were characterized by FTIR and 1H NMR spectroscopy, which showed that they had incorporated poly(propylene oxide) grafts into their structure. Their viscosity varied from 5 mPa,·,s to infinity, depending on the Lignin/PO ratio and their hydroxy index was in the range of 100,200, which made them suitable for rigid polyurethane foam (RPU) formulations. The RPUs thus obtained had a Tg of ca. 60,°C and a thermal conductivity of ,20 mW/m,·,K before ageing and ,25 mW/m,·,K after accelerated ageing for 10 d at 70,°C. The analyses of the gases inside the cells showed that these were mostly closed, since the partial pressure did not decrease significantly with ageing. Photograph of polyurethane foam made from OLOP. [source]


Composites of rigid polyurethane foam and cellulose fiber residue

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010
M. C. Silva
Abstract Rigid polyurethane composite foams were prepared with cellulose fibers as a filler. The cellulose fibers were an industrial residue of blanched cellulose pulp production. The influence of the cellulose fiber concentration on the structural, thermal, mechanical, and morphological properties of the foams was investigated. We also studied the influence of the cellulose fibers on the foam's resistance to fungal attack by placing a suspension of known fungus in contact with the surface of the foam and following the morphological evolution as a function of time (for 60 days). The increase in the cellulose filler concentration in the foams, up to 16% w/w with respect to the polyol, changed their properties as follows: (1) the cell size decreased, (2) the thermooxidative stability and mechanical properties remained approximately constant, (3) the thermal conductivity decreased slightly, and (4) fungal growth was observed. Therefore, a cellulosic fibrous industrial residue was rationally valorized as a filler in classical rigid polyurethane foams; this yielded materials with mechanical resistance and a susceptibility to fungi in a wet environment. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]


Oxypropylation of Lignins and Preparation of Rigid Polyurethane Foams from the Ensuing Polyols

MACROMOLECULAR MATERIALS & ENGINEERING, Issue 10 2005
Hamid Nadji
Abstract Summary: Different lignins were converted into polyols by a chain extension reaction with propylene oxide (PO). Thus, soda lignin from Alfa (Stipa tenacissima) (SL), organosolv lignin from hardwoods (OL), kraft lignin (KL) from softwood and oxidized organosolv lignin (OOL) were oxypropylated in a batch reactor at 180,°C in the presence of KOH as catalyst. The ensuing polyols were characterized by FTIR and 1H NMR spectroscopy, which showed that they had incorporated poly(propylene oxide) grafts into their structure. Their viscosity varied from 5 mPa,·,s to infinity, depending on the Lignin/PO ratio and their hydroxy index was in the range of 100,200, which made them suitable for rigid polyurethane foam (RPU) formulations. The RPUs thus obtained had a Tg of ca. 60,°C and a thermal conductivity of ,20 mW/m,·,K before ageing and ,25 mW/m,·,K after accelerated ageing for 10 d at 70,°C. The analyses of the gases inside the cells showed that these were mostly closed, since the partial pressure did not decrease significantly with ageing. Photograph of polyurethane foam made from OLOP. [source]


Formation and characterization of polyurethane,vermiculite clay nanocomposite foams

POLYMER ENGINEERING & SCIENCE, Issue 9 2008
T. Umasankar Patro
Nanocomposites of rigid polyurethane foam with unmodified vermiculite clay are synthesized. The clay is dispersed either in polyol or isocyanate before blending. The viscosity of the polyol is found to increase slightly on the addition of clay up to 5 pphp (parts per hundred parts of polyol by weight). The gel time and rise time are significantly reduced by the addition of clay, indicating that the clay acts as a heterogeneous catalyst for the foaming and polymerization reactions. X-ray diffraction and transmission electron microscopy of the polyurethane composite foams indicate that the clay is partially exfoliated in the polymer matrix. The clay is found to induce gas bubble nucleation resulting in smaller cells with a narrower size distribution in the cured foam. The closed cell content of the clay nanocomposite foams increases slightly with clay concentration. The mechanical properties are found to be the best at 2.3 wt% of clay when the clay is dispersed in the isocyanate; the compressive strength and modulus normalized to a density of 40 kg/m3 are 40% and 34% higher than the foam without clay, respectively. The thermal conductivity is found to be 10% lower than the foam without clay. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source]


Composites of rigid polyurethane foam and cellulose fiber residue

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010
M. C. Silva
Abstract Rigid polyurethane composite foams were prepared with cellulose fibers as a filler. The cellulose fibers were an industrial residue of blanched cellulose pulp production. The influence of the cellulose fiber concentration on the structural, thermal, mechanical, and morphological properties of the foams was investigated. We also studied the influence of the cellulose fibers on the foam's resistance to fungal attack by placing a suspension of known fungus in contact with the surface of the foam and following the morphological evolution as a function of time (for 60 days). The increase in the cellulose filler concentration in the foams, up to 16% w/w with respect to the polyol, changed their properties as follows: (1) the cell size decreased, (2) the thermooxidative stability and mechanical properties remained approximately constant, (3) the thermal conductivity decreased slightly, and (4) fungal growth was observed. Therefore, a cellulosic fibrous industrial residue was rationally valorized as a filler in classical rigid polyurethane foams; this yielded materials with mechanical resistance and a susceptibility to fungi in a wet environment. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]


Simulation of the percolation of water into rigid polyurethane foams at applied hydraulic pressures

POLYMER ENGINEERING & SCIENCE, Issue 7 2006
Pravakar Mondal
The hydraulic resistance of polyurethane foams is studied by means of simulations of water penetration into model foams. The model foams of cubical shape are constructed by generating the centers of the cells randomly. The strength of the window separating two cells is assumed to be a function of the distance between the centers of the cells in one set of computations. In another set of computations the strengths of the windows are assigned randomly from a specified distribution. The foam is exposed to an elevated pressure at its boundaries and water penetrates into the foam by rupturing the windows with strengths lesser than the applied pressure. The variation of equilibrium volume fraction of the foam filled with water for increasing hydraulic pressures shows typical percolation behavior: there is a sharp increase in the volume filled beyond a threshold pressure. Simulations show that beyond a certain sample size there is no change in the percolation curve with sample size, and indicate that it is mainly the weaker windows that control the hydraulic resistance of the foam. The simulation results are compared with experimental data. POLYM. ENG. SCI. 46:970,983, 2006. © 2006 Society of Plastics Engineers [source]