Experiment 4 (Full)
Experiment 4 (Full)
TECHNOLOGY
SCHOOL OF INDUSTRIAL TECHNOLOGY
UNIVERSITI SAINS MALAYSIA
IWA 383/2
PAPER TECHNOLOGY LABORATORY II
Experiment 3 : Chemical Effects in Kraft Pulp Recycling
Group : 5
Group Members : Lee Ying Fang
Farid Aiman Bin Nasir
Mohd Arif Bin Mohamad Samsudin
Lecturer
107979
107970
107990
1. Abstract
The main concept of this experiment is to determine the chemical effect in Kraft pulp
recycling.The type of recycled paper used is paper from Kraft pulp.The paper sample was
tear into small piecess and soak into four litres of water for at least four hours before
disintegration.Somehow,when the first soaking hour is up,the water is adjusted to the
appropriate desired pH by using diluted acid HCL and NaOH.The group which deal with
chemical hydrogen peroxide(H2O2) and alkaline peroxide (AP),the pH is maintain by
resultant pH.Then, the sample is disintegrated by disintigrator at 5000rpm and diluted the
pulp slurry to 0.3% consistency with filtered tap water and stir the diluted stock to ensure
proper mixing.The stock consistency and pulp freeness is then determine before forming
handsheets in 400 ml total fluid. The optical,mechanical and physical testing is carried out
such as brightness, opacity,thickness, tensile strength, bursting strength, tearing resistance
and folding endurance as recommended by the standard TAPPI procedure.Thus the amount
and quality of fibre bonding is the most important factor affecting the strength. Increased in
bonding caused by chemicals used also contribute in increasing the tensile strength as the
fibre contact area is increased.
2. Introduction
Paper recycling basically is the process of reused by taking the required fibrous raw
materials (pulps) and non- fibrous component (additives),treat and modify each furnish
constituent, and then combined all the ingredients continuously and uniformly into the
papermaking stock to produce paper.Usually for the enhancing the strength of paper, it will
mixed with fresh wood pulp or virgin pulp due to its long fiber properties. There are three
categories of paper that can be used as feedstock for making recycled paper which are mill
broke, pre-consumer waste, and post-consumer waste.
Paper cannot be recycled over and over again because since it turns into secondary
fibers, the strength properties surely will be drops due to case of fiber shortening. That is why
virgin pulp (long fiber) is usually mixed with recycled paper to support back the strength
properties of the paper. The repulping of the recycled paper is different from the virgin pulp
pulping process. More steps of removal contaminants are required to make sure the pulp will
be free from impurities. This is due to the raw material used in recycle paper is secondary
fiber which contain ink, stickiest, adhesive and etc. Thus, repulping process of secondary
fibre consume more chemical and high energy than virgin pulp pulping process.
Repulping is an important part for papermaking process because it will affect the
final yield for papers especially the strength properties. The purpose of repulper is to produce
low consistency pulp slurry usually ranges from 4.5-5% to broken down fiber particles, and
rendering the pulp more uniform. There is no cutting action on fibers.Optional chemicals
such as NaOH, HCL, AP or H2O2 are added by observing percentage of fibers swelling to
improve slushing by absorbing water to separate the fibers and thus high temperature are not
required, unless there is significant level of wet strength additive presents. In general, the
pulping process is continuous thus it will be agitated to form a slushy pulp of fiber. In pulping
system, the concept of disintegrated is done by vortex and shear forces which cause the fibre
to separate. The shearing forces only causing the fiber to swell due to water absorption and
tend to separate.In addition, the present of chemicals will contribute to the disintegrating of
fibres. The vortex intensity is dependent on pulp consistency. Thus, it provides more fiber
separation, control the level of consistency and increase uniformity of stock. One noticeable
effect of repulping is the spectacular alter on dewatering properties of the pulp. Pulp freeness
(CSF) is rapidly reduced as repulping proceeds, mainly due to the increased concentration of
fines. The freeness testing is to measure the freeness of pulp stock and stage of absorption
water for pulp.
The pH value for the aqueous medium is usually alkaline. The alkalinity results in the
softening and swelling of the paper fibers by saponification or hydrolysis which has to be
carefully determined for each furnish. The brightness increases with increasing pH but too
high pH will cause decrease in brightness. This phenomenon, called alkali darkening, has
been determined as due to the formation of chromophores in lignin. In the acidic condition,
low pH will also cause low brightness as acidic condition prevents the water penetration
inside fibre, hence, the fibre may not swell and the fiber will hard to disintegrate into
individual fibres. When the pH is neutral, there are no much different in brightness. Thus, a
careful balance is required in maintaining the right pH so that the fibers soften and swell up,
hydrogen peroxide performance is improved and formation of chromophores is minimized.
The handsheets was cut according to Figure 1 in Appendix B. Test of normal tensile, folding
endurance, burst, tearing strength, brightness and opacity were carried adapted from TAPPI
220.
i.
Bursting Strength
Specimen was placed and clamp between two concentric platens of Mullen tester, with each
having a circular opening in the centre. Pressure was applied to the underside of the specimen
by a rubber diaphragm which expands by the hydraulic pressure showed by the pressure
gauge.
ii.
Tensile Strength
Specimen was aligned and clamps between two jaws neatly an upper, moveable jaw and a
lower, stationary jaw. The upper jaw traverses upward at a constant rate when the test started.
The load (N) is recorded when the specimen break and calculated the tensile strength (N/m),
tensile index (Nm/g) and breaking length (km).
iii.
Tearing Resistance
Movable pendulum sector arc of Elmendorf tear test was fixed prior test in position from
which it can be released. The test specimen was fastened (a pile of 2 or 4 sheets) between the
two clamps with the bottom edge against nicely to the clamp bottom. An initial slit was made
and the sector arc was released from its fixed position. The energy required to tear the
specimen (mN) was recorded and the tear index based on the number of sheets used was
calculated.
iv.
Folding Endurance
The spring-loading jaw of the MIT testes was pressed with the appropriate weight (0.5-1.5
kg) and fastened the screw to fix jaw at level. The upper edge of the specimen strip was
clamped to the spring-loading upper jaw and the bottom edge was clamped to the oscillation
folding head firmly and neatly. The fold counter was reset and the screw of the upper jaw was
released. Folding test was started and recorded the folding endurance as a number of double
folds as shown by the counter.
3. Natural phenomenon
Recycling means repulp the fibers so many times and has been thought the fibre
swelling capability, and the flexibility of fibres will be reduce. The restricted swelling of
recycled fibres has been scribed to hornification. Hornification imply both a reduction in
the amount of water that fibers hold within their cell walls, and also a tendency for
rewetted fibers to be stiffer and less conformable than before being subjected to drying
or other kinds of stresses. Hornification also can be used when cellulosic fibers are
subjected to other kinds of stresses, including heating without drying as long as there is a
simultaneous loss of water-holding ability and strength potential.According to this concept
the process of repulping tends to open up submicroscopic spaces within the lamellar
structure of the fiber cell walls.Evidence of fibrillation during repulping includes swelling
in the thickness direction of fibers and also an increase in wet fiber flexibility.
In repulping system, the concept of disintegrated is done by vortex and shear forces
which cause the fibre to separate. The shearing forces only causing the fiber to swell due to
water absorption and tend to separate. The vortex intensity is dependent on pulp consistency.
In addition, the present of chemicals will contribute to the disintegrating of fibres.The
chemical added cause the fiber to swell. During the repulping process, the higher pH (alkaline
condition) is more preferable. This is because alkaline condition promotes the fibers to swell
easily than acidic condition. When the fibers swell, the water absorption of fibers increase,
thus the fibers become more flexible to disintegrated into individual fiber.
4. Methodology
2. With clean hands, the provided samples were tore down to small
size of 1.5cmx1.5cm. Moisture content was determined.
3. 48g OD of sample in (1) was weighed and soaked in 4L water for at
least 4 hours. When the first soaking hour is up, the suspension was
stirred and had it pH measured. Observation was recorded. The pH
was controlled to desired values. The pH value for every hour was
recorded.
4. The suspended pulp was disintegrated at 5000rpm. Colour was
recorded. Pulp slurry was diluted to 0.3% consistency and stirred
well.
5. The consistency of pulp stock for forming handsheet in 400ml total
fluid was calculated. Stock consistency was adjusted accordingly.
The pH of the prepared stock solution was measured. Colour change
was recorded.
6. After pulp freeness was determined, handsheet was made in the
amount recommended by the standard TAPPI procedure.
7. The wet handsheet which adheres on the blotting paper was dried
by placing the wet handsheet and the blotting paper on the hot
plate. A dry blotting paper was put on the wet handsheet and the
handsheet was dried by ironed. After the handsheet was fully dried,
the hot dry handsheet was removed from the blotting papers and
cooled down in a desiccator for 10 minute. A dry 100ml beaker was
placed in a digital analytical balance and the tare button was
pressed. The dry handsheet was taken out from the desiccator and
was placed into the tared beaker. The weight of the handsheet was
written down to the nearest 0.01g.
8. The drying and weighing steps were repeated until a constant
weight was obtained. The pulp consistency was calculated based on
the weight of the moisture-free handsheet. Based on the pulp stock
consistency calculated earlier:
i.
The volume of pulp stock required for producing a
handsheet with 60 grammage (60g/m 2) was calculated
ii.
or
The volume of the water which should be added or
removed from the pulp stock in order to adjust the
consistency to 0.30% was calculated.
9. The mesh and cylinder of the handsheet machine was cleaned and
the cylinder was then locked tightly. The pulp stock in the bucket
was stirred thoroughly and the required volume of pulp stock was
immediately measured by using a graduated cylinder. The measured
amount of the stock was poured into the sheet machine (cylinder)
and the start button was pressed to fill the cylinder with water. At
the same time, the graduated cylinder was rinsed with water and
the rinsed was poured into the sheet cylinder.
10.
The handsheet machine automatically release air bubble when
the water reach to the required level and then the water was
drained out from the handsheet cylinder to form a wet sheet on the
mesh. The cylinder was immediately unlocked and opened after the
water had drained from sheet. Two pieces of standard blotting
papers was placed on the drained sheet. The flat couch plate was
laid centrally on the blotting papers and couch roll was placed
gently on the middle of the plate. Without applying other pressure,
the roll was rotated backward and forward for five complete roll
within the range of 8 to 12 seconds. After that, the roll was lifted.
The handsheet, blotters and covering couch plate was removed
from the wire mesh. The sheet was adhered to the underside of the
lower blotter. The blotter with the adhered handsheet (handsheet
side up) was placed on two fresh blotters and was located centrally
on the press plate by using the press template. The handsheet was
covered with a polish plate (polished side down) and followed by two
fresh blotters which was ready to receive next couch blotter and
handsheet. The mesh in the sheet machine in positioned was
washed by turning on the water, occasionally the surface of the
mesh was rubbed with fingertips, and then the next test sheet was
made as described. About 10 sets of blotters, handsheet and plate
were stacked in the press plate.
11.
For first pressing, the cover of the press was placed in position
and the wing nuts were screwed hand-tight. The 1 st cycle button was
pressed and the pressure increased to 435kPa (50psig) in 30
seconds for duration of 5 minute. After the first pressing, the whole
stack was removed to one side. The plate and the sheet (handsheet
side up) were laid centrally on two dry blotters by using the press
template as a guide. The sheet was covered with two blotters and
the plate, sheet and blotters was laid continuously. The order of the
sheet was reversed in the second pressing. The cover was placed on
position as before and the pressure was raised within 30 second to
345kPa (50psig) for 2 minute.
12.
The stack was removed from the press and each plate with
the handsheet was fitted into the drying rings. The edge of each
handsheets was ensured to be in contact with the rubber of the next
ring above it. A heavy weight was placed on the pile of rings after
the whole stacks were fitted on the rings. The sheets were dried in a
standard conditioning room (as specified in TAPPI 402: 502% RH
and 231C). The sheets were left to become fully dried in position
in the rings before they were removed from the plates.
13.
Steps 2 to 12 is repeated using 24 od weight of pulp for
second recycling stage along with 2L of water for soaking.
4.3. Paper testing procedures
4.3.1.
Bursting Strength
Specimen was placed and clamp between two concentric platens of
Mullen tester, with each having a circular opening in the centre. Pressure
was applied to the underside of the specimen by a rubber diaphragm
which expands by the hydraulic pressure showed by the pressure gauge.
4.3.2.
Tensile Strength
Specimen was aligned and clamps between two jaws neatly an upper,
moveable jaw and a lower, stationary jaw. The upper jaw traverses upward
at a constant rate when the test started. Recorded the load (N) when the
specimen break and calculated the tensile strength (N/m), tensile index
(Nm/g) and breaking length (km).
4.3.3.
Tearing Resistance
Movable pendulum sector arc of Elmendorf tear test was fixed prior test in
position from which it can be released. The test specimen was fasten (a
pile of 2 or 4 sheets) between the two clamps with the bottom edge
against nicely to the clamp bottom. An initial slit was made and the sector
arc was released from its fixed position. The energy required to tear the
specimen (mN) was recorded and the tear index based on the number of
sheets used was calculated.
4.3.4.
Folding Endurance
The spring-loading jaw of the MIT testes was pressed with the appropriate
weight (0.5-1.5 kg) and fastened the screw to fix jaw at level. The upper
edge of the specimen strip was clamped to the spring-loading upper jaw
and the bottom edge was clamped to the oscillation folding head firmly
and neatly. The fold counter was reset and the screw of the upper jaw was
released. Folding test was started and recorded the folding endurance as
a number of double folds as shown by the counter.
Colour
Brightne
Coarsen
ss
ess
Brown
18.12
White
86.47
Slightly
rough
Smooth
Tappi
Opacity,
Opacity,
92.39
91.17
Gramma
Thicknes
Density,
ge, g/m
s, mm
g/cm
96.63
51.99
0.0876
0.59
93.19
72.72
0.0995
0.73
Freeness, ml
500
400
300
200
100
0
430.5
261
465
461
402.5
308
253
Group
6.2.2.
Optical properties
between fibres. The fibres will have better comformability giving better
bonding and less light scattering during the handsheet formation. Thus,
there will be lesser light being scattered around the fibres giving lower
opacity for handsheet produced from acidic recycling.
Furthermore, brightness of non-recycle handsheet has lower
brightness than recycled ones (Table 1)(Table 2). This is because the
usage of chemicals either acid or alkaline will give delignification effect
causing the reduction in chromophoric structure that absorbs blue light.
On the contrary, pulp that undergo recycling under neutral pH does not
show much changes since there is less swelling effect experience by
fibres.
Table 2: Final pH value of pulp stock for handsheet making and brightness
Group
Condition
Chemicals
Final pH
value
Brightness,
%
1
Acidic
HCl
2
Neutral
NaOH
3
Alkaline
NaOH
4
Neutral
H2O2
5
Alkaline
AP
6
Alkaline
AP
7
Alkaline
AP
4.07
7.25
7.11
6.40
10.12
10.54
10.22
23.46
23.39
23.43
23.98
22.70
23.56
26.08
97.1
7
6
98.59
98.8
97.35
98.69
Groups
98.34
99.26
Opacity P
98.84
99.25
3
2
98.31
98.35
95.5
99.61
96
96.5
97
97.5
98
Opacity, %
98.5
Opacity T
99.24
98.85
99
99.5
100
6.2.3.
Physical properties
Grammage,
g/m
59.39
60.91
64.50
70.50
64.34
60.42
60.97
0.6
0.5
0.4
0.3
0.2
0.1
0
1
Groups
6.2.4.
Mechanical properties
30
25
20
Tensile index
15
Tearing index
Burst index
10
folding endurance
5
0
1
Groups
fibres. Other than that, the removal of lignin in alkaline treatment exposed
cellulose chain causing the fibres to be more flexible results better
consolidation during handsheet formation. This gives lesser light
scattering effect.
28
27
26
25
Brightness, %
24
23
22
21
20
1
First recycling
Second recycling
96
95
94
93
92
1
First recycling
Second recycling
400
Freeness, ml
513 503
465
402.5
461
430.5
500
384
364
451444.5
395.5
308
300 261
253
200
100
0
1
First recycling
Second recycling
Mechanical properties
handsheet reduced after second recycling whereby the ability for the test
sample to resist rupture has lessened.
Based on Graph 9, burst strength and folding strength of
handsheets decreased after second recycling. This is because the
hornification effect after subsequent recycling and drying caused the fibre
to loss its ability to absorb water causing the fibre swell to certain extent
only. Since this phenomenon caused reduction in interfibre bonding, burst
strength of handsheet after second recycling drops since the fibres unable
to withstand the pressure applied onto the handsheet. Meanwhile, the
folding strength of handsheet decreased after second recycling occurred
because the fibre has loss its flexibility since the fibre unable to swell
during the rehydration process as there is no breaking of bond from fibres.
The latter fibre appears to be stiffer.
Furthermore, tearing strength of handsheet produced from second
recycling also decreased slightly compared to first recycling because the
effect subsequent drying from previous paper making process caused
thermaldegradation of cellulose chain. Besides, the frequent chemical
treatment caused the fibre to become brittle and lack of flexibility as well
as loss in bonding strength since the fibres only swell to certain extent.
This caused the handsheet produced to be rigid and the force applied onto
handsheet during tearing test only focus on small region resulting less
work required to overcome the frictional force between fibres.
30
25
20
15
10
5
0
1
First recycling
Second recycling
14
12
10
8
Mechanical properties
6
4
2
0
1
First recycling
Second recycling
6.3.4.
Physical properties
0.3
0.2
0.1
0
1
First recycling
Second recycling
Lightness
Top kraft
61.58
Test
60.79
A
b
Redness
Yellowness
6.18
19.81
4.01
15.61
7. Calculations
7.1. Alkaline Peroxide (AP) Recycling First and Second
Recycling
1. 0.5% NaOH
- Weight of pulp (OD) = 48g
-
0.5
48 g
100
0.24 g NaOH
2. 0.6% H2O2
- Given H2O2 = 10%
-
48 g
0.6
100
0.288 g
0.288 100
10
2.88 ml H 2 O 2
58.42=
AD 48
100
AD
AD =115.44 g
=115.44-48.00
=67.44g
=67.44ml
48
100
volume pulp
=11932.56ml
Handsheet Testing
Weight of pulp pad = 1.05g
Consistency=
1.05
100
400
Consistency=0.2625
.: The new volume of pulp required to produce 1.2g handsheet:
0.2625=
1.2
100
volume
volume=457.14 ml
.: value to be subtracted = 37
Pulp OD weight, g = 2.61g, volume used for freeness testing = 1000ml
2.61
100
1000
0.261
0.26
pH
10.73
10.47
10.35
10.27
10.12
Observation : pulp turn from dark brown to light brown after soak with
alkaline peroxide
7.5. Handsheet Making (Second Recycling)
OD weight of bleached pulp from second stage bleaching = 24g
Moisture content = 61.56%
Weight of wet pulp
61.56
AD24
100
AD
AD =62.43 g
Water in wet pulp
=62.43 - 24.00
=38.43g
=38.43ml
To Achieve Consistency 0.3% for Handsheet
0.3=
24
100
volume pulp
= 8 000 2 000
=6 000 ml
Handsheet Testing
Weight of pulp pad = 1.2305g
Consistency=
1.2305
100
400
Consistency=0.3076
2.72
100
1000
0.27
.: Based on T227, points of freeness to be subtracted = 21
Thus, correct CFS at 20OC, 0.3% consistency
= 510 - 38 - 21
=451ml
pH
10.85
10.68
10.54
10.35
10.23
7.8.1.1.
I.
Physical properties
Weight
Samples
1
2
3
4
5
Average
II.
Thickness
Sample
1
2
3
4
5
III.
Weight (g)
1.2879
1.2992
1.2360
1.2892
1.3213
1.2867
Thickness (mm)
Average
1
2
3
4
5
0.1371
0.1783
0.1400
0.1325
0.1378
0.1451
0.1429
0.1729
0.1424
0.1313
0.1550
0.1529
0.1359
0.1456
0.1311
0.1309
0.1434
0.1374
0.2009
0.1450
0.1354
0.1428
0.1331
0.1514
0.1781
0.1440
0.1498
0.1420
0.1440
0.1516
Average sum of 5 samples thickness 0.1477
Grammage
Grammage
Sample
1
2
3
4
5
Average
IV.
Density
,g
( m2g )= weightareaof ,paper
m2
Weight (g)
1.2879
1.2992
1.2360
1.2892
1.3213
1.2867
Grammage (g/m)
64.40
64.96
61.80
64.46
66.07
64.34
Sample
Weight (g)
Volume (cm)
1
2
3
4
5
Average
1.2879
1.2992
1.2360
1.2892
1.3213
1.2867
2.902
3.058
2.748
3.028
3.032
2.954
Density
(g/cm)
0.4438
0.4249
0.4498
0.4258
0.4358
0.4356
7.8.1.2.
I.
Mechanical properties
Tensile Strength
Tensile strength(um)=
load , N
strip width , m
Tensileindex
strength, um
( umg )= tensile
grammage , g /m2
*paper width=15mm=0.015m
tensile index
Breaking length ( km )=
, where um --> kg/m (divide by 9.807)
9.807
Sample
1
2
3
4
5
Average
II.
Load, N
20.3
19.7
19.2
17.9
12.1
17.84
Tear Resistance
Tearing index ,
Extension,
mm
3.7
3.4
3.4
2.7
1.5
2.94
Tensile
strength,
N/m
1353.33
1313.33
1280
1193.33
806.67
1189.33
Grammage
, g/m2
64.40
64.96
61.80
64.46
66.07
64.34
mN . m2 Tearing strength , mN
=
g
Grammage , g/m2
Tensile
index,
Nm/g
21.02
20.22
20.71
18.51
12.21
18.53
Breaking
length, km
2.14
2.06
2.11
1.89
1.25
1.89
Sample
Grammage, g/m2
1
2
3
4
5
Average
509.946
542.211
504.062
502.106
515.830
514.831
64.40
64.96
61.80
64.46
66.07
64.34
III.
(mN.m2)/g
7.9184
8.3468
8.1563
7.7894
7.8073
8.0017
Folding Endurance
Sample
1
2
3
4
5
Average
IV.
Tear index
Folding Endurance
5
4
3
4
5
4.2
Burst Testing
Burst index ,
Sample
1
2
3
4
5
Average
Burst strength,
Burst strength,
Grammage,
Burst index,
kgf/cm2
2.058
1.392
1.725
1.654
1.579
1.682
kPa
201.82
136.51
169.16
162.20
154.85
164.95
g/m2
64.40
64.96
61.80
64.46
66.07
64.34
kPa.m2/g
3.13
2.10
2.74
2.52
2.34
2.56
7.8.2.1.
I.
Physical properties
Weight
Samples
1
2
3
4
5
Average
II.
Thickness
Sample
1
2
3
4
5
III.
Weight (g)
1.2017
1.1959
1.2386
1.2570
1.2623
1.2311
Thickness (mm)
Average
1
2
3
4
5
0.1497
0.1236
0.1392
0.1447
0.1379
0.1408
0.2025
0.1361
0.1335
0.1433
0.1366
0.1505
0.1447
0.1361
0.1442
0.1369
0.1302
0.1387
0.1393
0.1430
0.1367
0.1323
0.1478
0.1400
0.1430
0.1458
0.1411
0.1358
0.1352
0.1404
Average sum of 5 samples thickness 0.1419
Grammage
Grammage
Sample
1
2
3
4
5
Average
IV.
,g
( m2g )= weightareaof ,paper
m2
Weight (g)
1.2017
1.1959
1.2386
1.2570
1.2623
1.2311
Grammage (g/m)
60.085
59.795
61.930
62.850
63.115
61.555
Density
Sample
Weight (g)
Volume (cm)
Density
(g/cm)
1
2
3
4
5
Average
1.2017
1.1959
1.2386
1.2570
1.2623
1.2311
20
20
20
20
20
20
0.4267
0.3976
0.4471
0.4496
0.4502
0.4338
7.8.2.2.
I.
Mechanical properties
Tensile Strength
Tensile strength(um)=
load , N
strip width , m
Tensileindex
strength, um
( umg )= tensile
grammage , g /m2
*paper width=15mm=0.015m
tensile index
Breaking length ( km )=
, where um --> kg/m (divide by 9.807)
9.807
Sample
Load, N
1
2
3
4
5
Average
II.
Extension,
mm
15.3
14.2
17.9
18.8
10.5
15.34
2.1
2.1
2.1
3.1
1.5
2.18
Tear Resistance
Tearing index ,
Tensile
strength,
N/m
1020.00
946.67
1193.33
1253.3
700.00
1022.67
Grammage
, g/m2
60.085
59.795
61.930
62.850
63.115
61.555
Tensile
index,
Nm/g
16.98
15.83
19.27
19.94
11.09
16.61
Breaking
length, km
1.731
1.714
1.965
2.033
1.131
1.694
mN . m2 Tearing strength , mN
=
g
Grammage , g/m2
Sample
Grammage, g/m2
1
2
3
4
418.744
490.333
467.777
445.222
60.085
59.795
61.930
62.850
Tear index
(mN.m2)/g
6.96919
8.20023
7.55332
7.08388
5
Average
III.
63.115
61.555
450.125
454.440
Folding Endurance
Sample
1
2
3
4
5
Average
IV.
7.13183
7.38769
Folding Endurance
3
2
4
4
3
3.2
Burst Testing
Burst index ,
Sample
1
2
3
4
5
Average
Burst strength,
Burst strength,
Grammage,
Burst index,
kgf/cm2
1.508
1.357
1.463
1.488
1.397
1.443
kPa
147.880
133.080
143.470
145.920
136.999
141.510
g/m2
60.085
59.795
61.930
62.850
63.115
61.555
kPa.m2/g
2.461
2.226
2.317
2.322
2.171
2.299
7.8.3. Brightness and opacity of handsheet from first and second recycling
8. Conclusion
Based on the experiment conducted, the effect of chemicals on subsequent paper
recycling shows reduction in papers properties in terms of strength but the brightness of
paper after recycled shows increment after treated with chemicals. The reduction in papers
strength is due to hornification effect causing the fibres unable to swell and flexible. Thus,
rapid recycling process under chemical treatment cause the paper properties to be lower since
there is lack of interfiber bonding between fibres. Meanwhile, paper brightness increases
because there is reduction in chromophoric structure and delignification effect by the
chemicals used.
However, the strength properties of handsheet produced from first recycling still shows
increment compared to non-recycled ones since chemical used like alkaline peroxide promote
better delignification compared to normal alkaline treatment. Even so, other condition also
showed increment in paper strength but the impact is not as obvious as alkaline peroxide
treatment.
9. Reference
1. http://www.ncsu.edu/bioresources/BioRes_02/BioRes_02_4_739_788_Hubbe_VR_R
ecycling_Cellulosic_Fibers_Review.pdf
2. http://upcommons.upc.edu/e-prints/bitstream/2117/6356/1/effects-of-drying.pdf
3. Gary A. Smook, second edition, Handbook for Pulp & Paper Technologists.
4. http://www.cellulosechemtechnol.ro/pdf/CCT1-3-2009/p.65-69.pdf
5. Wistara, N. and R. Young, Properties and treatments of pulps from recycled paper.
Part I. Physical and chemical properties of pulps. Cellulose, 1999. 6(4): p. 291-324