© 2002 Elis Nina Herliyana Posted
29 November, 2002
Makalah Pengantar Falsafah Sains (PPS702)
Program Pasca Sarjana / S3
Institut
Pertanian Bogor
November 2002
Dosen:
Prof. Dr. Ir. Rudy C. Tarumingkeng
(Penanggung Jawab)
Prof. Dr. Zahrial Coto
Dr. Bambang Purwantara
Biobleaching of Wood Pulp of Acacia Aangium and Pinus
merkusii using Phanerochaete
chrysosporium
By:
ABSTRACT
The
white-rot fungi Phanerochaete chrysosporium
was tested to identify the ability for the biobleaching of wood pulp of Acacia mangium and Pinus merkusii. This
research was carried out in the laboratory of Forest Pathology and Laboratory
of Bioindustry, Bogor Agricultural University, Indonesia. The bleaching process
of pulp that used in this experiment is "Solid Media Cultivation
method". The experiment was
conducted in "bio-reactor" with different condition. Each bioreactor
was filled with 100 gram pulp, 100 ml PDL (Potato dectros liquid) and 10 gram
inoculum of fungi. The incubation period were
0, 2, 4, 6, and 8 week. The result showed that P. chrysosporium could increase significantly the brightness of
pulp of A. mangium from 54,6 % to
67,5 % and pulp of P. merkusii from
43,3 % to 60,3 %.
INTRODUCTION
The
production of pulp in many countries in this moment is still produced throught
chemically, especially with sulfatisation. This is due to the fact that
chemical method have advantages compered with other methods, for examples,
among them very quickly and high quality of pulp. But in this moment, pulp which produced by sulfat process have
not interested, because in the beginning.
We
needed high investation and color of pulp was dark and the danger of polution
of environment could be float to the surface. The industri of pulp and paper
was knowed as sources of pollution of Environment, especially at bleaching pulp
process (Casey 1980; Jurasek & Paice 1990). The aplication of biotechnology
by using fungi-decomposed lignin was needed to study as
one of alternativ for bleaching pulp process. Some fungi that used to process bleaching were Coriolus versicolor (Paice et al 1989; Jurasik & Paice 1990;
Ruhendi et al 1993), Phanerochaete chrysosporium (Kirk &
Yang 1979), Phabia radiata (Viikari et al 1986). The aim of bleaching was to
reduce residu lignin and other dye (kromofor) progresifly and to increase
brightness of pulp.
The
objective of the research was to study the effect of P. chrysosporium for bleaching pulp of wood Acacia mangium and P.
merkusii.
Preparation of pulp sulphate
The
sample pulps for this experiment were P.
merkusii and A. mangium. The process of pulping was done by sulfidity
25 % and the alkali activ for P. merkusii
was 18 % and for A. mangium was 16
%. The kappa numbers of A. mangium pulp was 9,48 and Kappa
number of P. merkusii pulp was 14,37.
The biobleaching process
The
biobleaching process of pulp in this experiment was used " Solid Media
Cultivation Method". The
experiment was conducted in " bio-reactor" with different conditions,
with aeration and non-aeration. The
aeration condition was flowted with air flowing 2,4 l/minute. Each
"bioreactor" was stored in incubator under room temperatur. The
optimum temperatur of the fungi were 26-300C. Temperatur in
"bioreactor" were adjusted approximetly 25-26oC. The humidity in incubator were about 74-92%
(means of RH was 80%) and the humidity in the "bio-reactor" was
adjusted + 90 %. Each treatment
were repeated three replications.
Each
"bioreactor" was filled with 100 grams pulp, 100 ml PDB (Potato
dextrose Broth) and 10 grams inoculum of fungi. The period of incubation were adjusted 0,2,4,6 and 8 weeks. The
PDB was added with source N optimum and pH optimum (from result of study of
growth of fungi). Source of N optimum
was glisine with N contents 50 mg/l.
The optimum growth of P.
chrysosporium was in pH + 6.
In other than, pH of substrat after sterilisation in autoclav had
chanced become 5,88 on pulp A. mangium
and 6,44 on pulp P. merkusii.
During
the test period, content of lignin, kappa number and brightness of the pulp were determined, and pH was measured. The content of lignin of the pulp was
determined by using the spektrofotometri method (Johnson, Moore & Zank
1961; Bagby, Cunningham & Maloney 1973).
The kappa number of pulp was determined by using the SII 0530-81
method. The brightness was determined
by using the SII 043781 methods. And
the pH of pulp was measured with pH-meter (Gumbira-Said 1992).
RESULTS AND DISCUSSION
After
bleaching pulp A. mangium and P. merkusii with P. chrysosporium, kappa number of pulp A. mangium and P. merkusii
with P. chrysosporium were decreased
on aeration or anaeration condition (Bild 1).
The reduction of kappa numbers of both pulps above were in the same
times with the reduction of content of lignin and the increasing brightness
both of pulps. P. chrysosporium had been
knowed that it can produce enzim who it can degrade content of lignin of wood
or of pulp (ligninase, xilanase and selulase) (Highley & Kirk 1979). P. chrysosporium can produce ligninase or lignin peroksidase
(Tien & Kirk 1983, Glen et al
1983 in Trotter 1990).
Result
of analisis statistic showed that kappa number of pulp A. mangium less significan than kappa number of pulp P. merkusii.
After
8 weeks incubation, the application of P.
chrysosporium on the pulp reduced the pH of Acacia pulp from 5.8 to 4.3 and reduced the pH of Pinus pulp from 6.4 to 4.3.
Content
of lignin pulp A. mangium and P. merkusii were reduced significant of
both conditions (aeration and anaeration) (Bild 2).
Pelliner
et al 1989 (in Reid et al 1990) reported that P. chrysosporium delignificated on pulp
of nadle blat wood. The kappa numbers
means showed content of lignin too (Anonim 1991).
Brightness pulp A. mangium and
P. merkusii increased significant of
both conditions (aeration and anaeration) (Bild 3). The result showed that P. chrysosporium could increase
significantly the brightness of pulp of A.
mangium from 54,6 % to 67,5 % and pulp of P. merkusii from 43,3 % to 60,3 %.
From
the results of this study, it can be concluded that: P. chrysosporium have potention als biobleaching agent, because it
can increased brightness of pulp A.
mangium from 54,6% to 67,5% and it can increased brightness of pulp P. merkusii from 43,3% to 60,3% after 6
weeks incubation. The optimal time of
incubation was 6 weeks. The result of
statistic anality showed that on this time lignin content of pulp was minimum,
and brightness was maximum. But the
kappa numbers on this time were not significanly. The environment of process of aeration was not influenced obvious
to kappa number, lignint content and brightness. The assumption was volume and
distribution of air in this experiment minus.
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