Properties of Particleboard Made From Ru
Properties of Particleboard Made From Ru
Properties of Particleboard Made From Ru
Composites: Part B
journal homepage: www.elsevier.com/locate/compositesb
a r t i c l e i n f o a b s t r a c t
Article history: The objective of the study was to evaluate physical and mechanical properties of experimental
Received 11 April 2012 particleboard panels made from rubberwood (Hevea brasiliensis) using modified starch as binder. Panels
Received in revised form 8 November 2012 were manufactured using 15% corn starch modified with glutardialdehyde and tested for their properties
Accepted 24 February 2013
based on Japanese Standard. The modulus of rupture and the internal bond strength of the panels met the
Available online 4 March 2013
requirement of the specified standard. Based on the findings in this work modified corn starch can have a
potential to be used as binder to produce particleboard panels with acceptable properties.
Keywords:
Ó 2013 Elsevier Ltd. All rights reserved.
A. Wood
D. Mechanical testing
D. Surface analysis
1359-8368/$ - see front matter Ó 2013 Elsevier Ltd. All rights reserved.
http://dx.doi.org/10.1016/j.compositesb.2013.02.020
260 M.H.M. Amini et al. / Composites: Part B 50 (2013) 259–264
materials such as corn, potato, rice, wheat, sago and many more on 15 samples with 3 readings taken for each samples using the Hom-
and widely available throughout the world commonly used in food mel Tester T500, which consists of the main unit and the pick up model
industries. Therefore, modification of starches were well docu- TkE. The pick up has a skid type diamond stylus with 5 lm tip radius
mented by many researchers [7]. Various modifications of starch and a 90° tip angle. The stylus moves over the surface at constant speed
were evaluated, including through oxidation, esterification, ether- of 1 mm/s over 15.2 mm tracing length. Vertical displacement of the
ification and crosslinking of starch. These processes yield, for stylus was converted into an electrical signal. Three roughness param-
example carboxymethyl starch, dialdehyde starch, hydroyethyl eters, i.e., average roughness (Ra), mean peak-to-valley height (Rz), and
starch and starch xanthate [8]. Besides for food industries applica- maximum roughness (Rmax) were used for surface roughness evalua-
tion, utilization of starch in non-food industries was also investi- tion of the samples. Specifications of these parameters were discussed
gated by researchers, especially in the biodegradable in previous studies [5,13,14]. Determination of surface roughness is
thermoplastic field [9]. Although properties of rubberwood parti- important as some coating materials really depend on the surface of
cleboard have been investigated in various works, currently there the panels to work. Scanning electron microscopy (SEM) analysis
is no information on characteristics of composite panels made was also carried out to see the interaction and distribution of the adhe-
from rubberwood manufatured by modified starch as binder sive between the wood particles.
[1,10]. Therefore the objective of the work was to manufacture Characterizations of chemical and thermal properties of the
experimental panels from rubberwood and modified starch, and manufactured particleboard were done. Infra-red spectra in the
to evaluate both physical and mechanical properties of the samples range of 4000–470 cm1 of the particleboard were measured with
to determine if they were similar to those of commercially manu- FTIR spectrophotometer, (Nicolet, AVATAR FTIR-360), running Om-
factured particleboard panels. nic software, to characterize the functional group inside the parti-
cleboard. To evaluate the crytallinity of the materials inside the
particleboard, finely powdered samples were prepared from the
2. Materials and methods IB test specimen, examined by XRD analysis using Diffraktometer
D5000 Kristalloflex, Siemens. Step scan measurements were done
Commercially produced rubberwood ( H. brasiliensis) particles using X-rays (Cu–Ka) at 40 kV and 40 mA. Scanning of 2h was ran-
supplied by a local particleboard company in Negeri Sembilan, ging from 10.0° to 40.0° corresponding to scanning speeds of 0.02°/
Malaysia were used to make experimental panels. The particles min and 2°/min [15]. The crystallinity index (C Ir) was calculated
were dried to 2% moisture content in a laboratory type oven. Corn using the formula:
starch in powder form modified with glutaraldehyde in liquid form
in a ratio of 1:2 (w/w) was used as binder in a ratio of 15% based C Irð%Þ ¼ ðI200 Iam Þ=I200 100 ð1Þ
oven dry particle weight. Initially corn starch powder was dis-
solved in distilled water with a temperature of 30 °C before it K k
L¼ ð2Þ
was stirred and added 25% glutardialdehyde solution. Glutardial- b cos h
dehyde (GDA) is a colorless oily liquid organic compound with
where I200 is the peak intensity corresponding to crystalline and
the formula of CH2 (CH2CHO)2. It is widely used as disinfector
Iam is the peak intensity of the amorphous fraction.
agent for medical equipment. It has specific density ranging from
Thermal decomposition of the manufactured particleboards
1.06 to 1.12 at 20 °C [11].
was done using a Metler Toledo TGA/SDTA 851 thermogravimetric
A total of 15 panels, five for each density level with dimension
analyzer, recorded from 30 °C to 800 °C for samples of 5–10 mg
of 20.1 cm by 20. 1 cm by 0.5 cm was manufactured for the exper-
placed in an aluminum pan with a heating rate of 20 °C min1 un-
iments, as shown in Table 1. Panels were made for target density
der a nitrogen atmosphere [16]. Differential scanning calorimetry,
levels of 0.60 g/cm3, 0.70 g/cm3 and 0.80 g/cm3. Fifteen percent
(DSC) Pyris 1, Perkin Elmer was used to evaluate the thermal
modified corn starch was manually mixed with rubberwood parti-
behaviors of the manufactured particleboards, with heating rate
cles before they were processed in a computer control press using a
of 10 °C/min. About 7 mg of powdered particleboard was added
pressure of 5 MPa at a temperature of 165 °C for 20 min. Panels
to an aluminum pan and sealed. An empty, sealed aluminum pan
were conditioned in a climate chamber with a temperature of
was used as reference. Then it was heated from 10 °C to 280 °C
20 °C and a relative humidity of 65% for 2 weeks. After the samples
at the respective heating rate. Melting temperature of particle-
were conditioned, their modulus of elasticity (MOE), modulus of
board was determined from the obtained DSC curve.
rupture (MOR), internal bond strength (IB), thickness swelling,
water absorption and surface roughness were evaluated based on
Japanese Industrial Standard [12]. 3. Results and discussion
Both bending and internal bond strength test were carried out on
using Tensile Strength Tester Machine Model 5582 (INSTRON) Table 2 displays test results of the samples. The highest average
equipped with a load cell having 1000 kg each. Crosshead speeds of values of 3541 N/mm2 and 20.38 N/mm2 were found for MOE and
10 mm/min and 2 mm/min were used for bending strength and inter- MOR of the panels with density of 0.80 g/cm3, respectively. These
nal bond strength, respectively. Thickness swelling and water absorp- values were 59.41% and 58.35% higher than those of the specimens
tion test were carried out by soaking 50 mm 50 mm 5 mm made with 0.70 g/cm3 target density. The samples produced with
samples in water for 2 h and 24 h. Surface roughness profile were done 0.60 g/cm3 density level resulted in the lowest bending properties
Table 1
Experimental design.
Table 2
Test results with statistical analysis of the samples.
Target density Measured Bending test (N/mm2) Internal bonding Thickness swelling, % Water absorption, % Surface roughness, lm
(g/cm3) density (g/cm3) (N/mm2)
MOE MOR 2h 24 h 2h 24 h Ra Rz Rmax
0.60 0.58 (0.03)a 1967.07 9.85 0.62 (0.11)a 28.76 39.087 87.35 106.01 3.62 41.69 50.65
(349.50)a (2.43)a (6.75)a (5.92)a (8.55)a (3.9)a (0.97)a (8.28)a (13.15)a
0.70 0.69 (0.04)b 2221.28 12.87 0.88 (0.21)b 34.81 47.53 90.02 107.42 3.64 37.51 52.92
(336.44)a (2.44)b (7.38)b (10.64)b (11.26)a (8.31)a (1.23)a (8.63)ab (11.1)a
0.80 0.78 (0.07)c 3540.97 20.38 1.02 (0.26)b 45.77 60.80 91.09 107.58 2.86 35.15 50.3
(475.22)b (3.55)c (7.32)b (8.13)b (6.37)a (6.89)a (1.13)b (9.13)b (9.07)a
1736.41
1646.46
2928.69
B
I002
Secondary
Secondary
peak
peak
Iam
Fig. 2. FT-IR spectra (A) and XRD spectra (B) of glutardialdehyde modified starch particleboard sample made using glutardialdehyde modified corn starch as a binder.
1646.46 cm1, in aldehyde and ester form, respectively, as shown sharp decrease of weight as the sample was heated from 250 °C
in Fig. 2A. These chromophores shows the presence of glutardial- to 425 °C which is from 91.7% to 25.69%, a 66.01% weight decre-
dehyde modified corn starch as the binder in the particleboard ment. This large weight loss was probably due to the thermal
[21]. An XRD spectrum in Fig. 2B. shows that the powder of glutar- decomposition of hemicellulose, carbon dioxide and water [16].
dialdehyde modified corn starch was highly amorphous. Major The TG profile also showed that the ash content of the particle-
intensity peaks at 2h was observed near 23° related to their crystal- board is lower than 18.43% as longer heating and higher tempera-
line structure. Secondary peaks were also observed at 2h = 15° and ture could increase decomposition of sample. The DTG profile
2h = 20.5°. The crystallinity index was calculated to quantify the showed a detail view of the analysis. The DTG shows rate of
crystallinity of the sample, yielded as 70.59%. decomposition or mass loss at certain temperature [22]. Water loss
Fig. 3A and B illustrate the weight loss curves (TG) and deriva- is highest at 43 °C while thermal degradation of sample was at the
tive thermogravimetric (DTG) profiles of the modified corn starch highest rate at 360 °C, determined as 0.15 %/min. From differential
particleboard. A slight 6% weight loss between the 30 °C and scanning calorimetry analysis of manufactured particleboard sam-
100 °C was due to loss of moisture from the sample. There was a ples, two exothermic peaks were found at 32 °C and 172 °C. There
M.H.M. Amini et al. / Composites: Part B 50 (2013) 259–264 263
A 4. Conclusions
100 91.7%
From the results, the highest and lowest modulus of elasticity
values were determined as 3540 MPa and 1967 MPa for the panels
80 with 0.80 g/cm3 and 0.60 g/cm3 density levels, respectively. Inter-
nal bonding strength showed the same trend, highest at 1.02 N/
Weight (%)
mm2 for 0.80 g/cm3 panels and lowest at 0.62 N/mm2, measured
60
from 0.6 g/cm3 panels. Thus, it can be concluded that these panels
satisfied the Japanese Industrial Standard. The dimensional stabil-
40 ity of the panels towards moisture needs to be improved by
addition of water repellent materials or the manufactured particle-
25.69%
boards should be restricted to only dry condition usage. Consider-
20 ing all the parameters above, glutardialdehyde modified corn
starch has the possibility to be commercialized as wood binder
50 100 150 200 250 300 350 400 450 500 550 600 650 700 in particleboard industry.
Temperature (°C)
B Acknowledgement
0.00
The authors were thankful for the Ministry of Higher Education
of Malaysia for the MyPhd funding to Mohd Hazim Mohamad Ami-
Derivative weight (1/min)
ni. The authors also acknowledged Universiti Sains Malaysia for the
-0.05 Research University Grant (1001/PTEKIND/815066) to Rokiah Ha-
shim and Postgraduate Research Grant Scheme (1001/PTEKIND/
844104) for Mohd Hazim Mohamad Amini. Appreciation was also
-0.10 given to the Heveaboard Sdn Bhd for providing the raw materials
for particleboard making.
-0.15 References
[20] Hiziroglu S, Kosonkorn P. Evaluation of surface roughness of Thai medium [22] Hermawan D, Hata T, Umemura K, Kawai S, Nagadomi W, Kuroki Y. Rapid
density fiberboard (MDF). Build Environ 2006;41(4):527–33. production of high-strength cement-bonded particleboard using gaseous or
[21] Wade LG. Organic chemistry. 6th ed. New Jersey: Pearson Education Inc.; 2006. supercritical carbon dioxide. J Wood Sci 2001;47(4):294–300.
p. 1330.