Fire-retarding polyurethane (PU) composite was produced by adding 2,4-ditert-butylphenyl phosphite (FR) to palm-based monoester resin with loading percentage of 0, 2, 4, and 6 wt%. The Shore D hardness index increased marginally with increasing FR content. However, the impact and flexural strengths decreased with increasing FR loading attributed to the weak interfacial bonding between FR and PU matrix. The fire test indicated lowering of burning rate (from 5.30 mm.s-1 to 2.80 mm.s-1) as the loading percentage of FR increased. The combustion enthalpy of the composites also decreased with higher loading percentage of FR.
In this report, we demonstrate that continuous improvement in XPS instruments and the calibration standards as well
as analysis with standard component-fitting procedures can be used to determine the binding energies of compounds
containing phosphorus and sulfur of different oxidation states with higher confidence. Based on such improved XPS
analyses, the binding energies (BEs) of S2p signals for sulfur of increasing oxidation state are determined to be 166-167.5
eV for S=O in dimethyl sulfoxide, 168.1 eV for S=O2
in polysulfone, 168.4 eV for SO3
in polystyrene sulfonate and 168.8
eV for SO4
in chondroitin sulfate. The BEs of P2p signals show the following values: 132.9 eV for PO3
in triisopropyl
phosphite, 133.3 eV for PO4
in glycerol phosphate, 133.5 eV for PO4
in sodium tripolyphosphate and 134.0 eV for PO4
in sodium hexametaphosphate. These results showed that there are only small increases in the binding energy when
additional oxygen atoms are added to the S-O chemical group. A similar result is obtained when the fourth oxygen or
poly-phosphate environment is added to the phosphorus compound. These BE values are useful to researchers involved
in identifying oxidation states of phosphorus and sulfur atoms commonly observed on modified surfaces and interfaces
found in applications such as biomaterials, super-capacitors and catalysis.