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3.1.4 Biodegradability
Biodegradability refers to the ability of a material to decompose after interactions with
biological elements. Many plastics are highly stable and are slower to biodegrade.
Developments in the use of green (biodegradable), recycled and biopolymer materials 99
These nondegradable plastics accumulate at the rate of 25 million tonnes per year,
with plastic-based nonwovens forming part of this number (Pometto and Lee,
1992). Biodegradable polymers that are designed to break down in landfill, compost-
ing and anaerobic treatment plants are of interest, as they can be tailored to degrade at
the end of their useful life and will not to persist in the environment for extended
periods.
3.1.5 Recycling
The ability to recycle nonwoven materials is seen as a significant means of increasing
product sustainability by reducing the volume of nonwovens going to landfill or incin-
eration. Polyethylene (PE) and polyethylene terephthalate (PET), common materials in
the production of nonwovens, are easily processed through municipal recycling and
sorting streams, and sorted material can be redirected to the production of new
products.
The sustainability of a nonwoven product can be evaluated by considering each
aspect, along with impact of production and distribution. A truly sustainable product
will deliver tangible benefits to the consumer whilst minimising the negative impact on
the environment. This costebenefit ratio is usually measured using a holistic life cycle
assessment. Due to the various factors involved, defining the most sustainable option is
not always straightforward and may require numerous assumptions or estimations.
When life cycle assessments are used, it can reveal unexpected results. For example,
nonwovens formed from conventional PET and PE require the consumption of a
nonrenewable resource; however, the benefits in performance and lifespan of these
products, combined with ease of recycling, mean that the commodity plastics can be
the most sustainable option and bring significant ecological benefits (Pourdeyhimi,
2011). This is an important consideration as polyolefins and PET dominate the market,
occupying 95% of the polymer-to-web sector in 2011 (Wiertz, 2014).
reached the end of their functional life. Typical time spans for a product to be consid-
ered biodegradable is 3 years for decomposition in a natural biological environment
(Kyrikou and Briassoulis, 2007). However, there are multiple environments in which
biodegradation can occur: landfill/soil burial; anaerobic digestion; composting and
marine and aquatic environments, which expose the materials to different ambient
conditions. Various test mechanisms exist, and the standard requirements and assess-
ment methods for biodegradability and compostability are listed in various interna-
tional standards (EN 13432:2000, ASTM D6400). For the majority of products, soil
burial and composting will be the primary measure for biodegradation.
Polymers that are disposed in landfill may become exposed to enhanced levels of mois-
ture, heat, electromagnetic energy (visible light and UV radiation), external forces and
chemicals. The combination of physical and biological degradation can lead to a complete
breakdown of the material to base elements such as CH4, CO2 and SO4 (Fedorak, 2005).
Physicalechemical degradation caused by moisture, heat, light and aggressive environ-
ments act faster than biodegradation, but it is often the latter that is needed to complete
the final step of mineralisation. The commodity polymers are difficult and slow to degrade
due to unreactive backbones that do not respond to biological attack.
There are two principle groups of organisms that can break down organic matter:
bacteria and fungi. The biological process may be either aerobic or anaerobic, depend-
ing on the local conditions and availability of oxygen. Each polymer will have a typical
degradation period depending on the environment; for cotton, this could be less than a
year, but for polyolefins, the timeframe for biodegradation could be hundreds of years
(Arutchelvi et al., 2008).
Composting, along with recycling and incineration, is being developed in many
countries as an alternative to disposal in landfill. A composting environment can facil-
itate polymer breakdown and accelerate the decomposition of polymers that are slow
to break down with conventional landfill and soil environments. Ingeo PLA (polylactic
acid) produced by Natureworks is marketed as being compostable (Natureworks,
2015). Composting can speed up the natural breakdown of cleavable polymer chains
such as Viscose and Tencel but is less effective on resilient polymers such as PE, PP
and PET (Gulich et al., 2014; Lenzing, 2010; M€ uller et al., 2001)
Composting on an industrial scale requires significant infrastructure and is less suit-
able for agrotextile and geotextile nonwovens. However, when the polymer product is
marked as compostable, it can enter municipal processing streams through domestic
organic waste collection services, allowing materials to be broken down but also
contribute to the volume of compost produced. For example, the Biofibrocar project
developed by AITEX, Spain, proposed using PLA and PLA/hemp nonwovens in auto-
motive interiors and door linings designed to be reclaimed and composted upon
disposal of the car (Gulich et al., 2014).
can be broken down in an efficient compost heap in 1e6 months (Li et al., 2010). This is
due to the presence of the glycoside bond that is open to depolymerisation through inter-
action with enzymes (Fedorak, 2005); the organisms then consume the resulting sugar
glucose products. Wool is a more resilient protein fibre but is also digested with bacteria
and fungi, along with insect larva, and can fully degrade in a soil burial after 6 months in
the ground (IWTO, 2015). The biodegradability of natural materials means there is more
concern regarding the cultivation and processing of natural fibres than the end-of-life
impact. For example, the cotton plant is notoriously thirsty, and wool requires a water
intensive scouring process to remove natural grease and impurities before processing.
Alternative natural materials, such as bast fibres, combine biodegradability with a
significantly lower carbon and water footprint, along with desirable physical properties.
This has led to them being used increasingly for needle-punched nonwovens for agricul-
tural and insulation applications (Choudhury, 2010).
Similar to the bast fibres, fibres derived from plant leaves can also be formed into
biodegradable nonwovens. One example of this is the Pinatex nonwoven, currently
used as a backing for imitation leather and produced from pineapple leaves, which
are a waste material that are otherwise sent for disposal (Ananas-Anam, 2014). How-
ever, natural materials comprise only 3% of the fibre-based nonwovens market, and so,
their combined impact on the environment is less of a concern than man-made mate-
rials (Wiertz, 2014).
3.2.3 Synthetics
In the main, the synthetic fibres exhibit poor biodegradability and tend to persist for
excessive periods in the environment. The technical requirement for plastics to be sta-
ble and retain performance in a range of environments has led to a generation of
high-performance stabilised polymers and nonwovens, which are highly resilient
and unaffected by the levels of physical, chemical and biological attacks typical of
landfill and dumping sites. The rate of biodegradation after soil burial and landfill
of the primary man-made polymers varies, ranging from negligible/nonexistent for
PET and PE, over many years to 8 days for the 95% degradation of Lyocell (Lenzing,
2010). In between these two extreme examples are materials such as polycaprolactone
(PCL) and PLA, the former taking 6 weeks for 95% degradation when buried in soil in
conditions typical in landfill (Gouda et al., 2012).
For a wide range of products, it is desirable to biodegrade at a much faster rate than
conventional synthetic materials in order to minimise the long-term effects on the envi-
ronment. The regenerated cellulosic fibres produced through the viscose rayon and
Lyocell routes could be considered the first biodegradable synthetic fibres (Kyrikou
and Briassoulis, 2007). Like with natural cellulosic fibres, enzymatic processes also
cleave the backbone of these fibres. Regenerated cellulosic fibres are currently used
to create sustainable disposable nonwovens for sanitary and hygiene applications
that break down in waste treatment plants (INDA, 2012). More recently, there have
been new developments in the production of eco-friendly PET and other materials
with purported biodegradability. Aliphatic polyesters, such as PCL, are vulnerable
to attack by bacteria and fungi, breaking it down to water-soluble products (Nishida
102 Advances in Technical Nonwovens
and Tokiwa, 1993). Research has also been published that suggest that poly(ester
amide)s (PEA) could combine good thermal and mechanical performance with biode-
gradability (Fonseca et al., 2014). PEAs have been formed into nonwovens for highly
specialised tissue engineering applications where biocompatibility is more important
than sustainability (Hemmrich et al., 2008). Pilot studies have shown that PEA can
be melt processed on a spunbond line with commercially viable extrusion rates of
2000e6000 rpm, making them potentially high-volume, low-cost materials (T€andler
et al., 2001). In addition to these aforementioned polymers, there are numerous niche
and novel materials that biodegrade that are currently being used for specialist appli-
cations. One example is the use of collagen and gelatine in technical nonwovens,
currently used in biomedical applications, but could find use in domestic and dispos-
able applications where rapid breakdown of product is required.
example of this is the recycling of PET bottles to form new products, including
textile fibres. For most applications, the performance of recycled-PET (rPET) fibres
mirrors that of the virgin product. This holds true for many nonwovens, as Poole
Company, USA, reported that recycled wipes have virtually the same performance
characteristics as virgin PET products (Nonwovens-Industry, 2014). As there is
no polymerisation step, the use of rPET is estimated to have an energy use of
66 MJ/kg of fibre compared to 125 MJ/kg for virgin PET and 250 MJ/kg for virgin
nylon (O Ecotextiles, 2009). However, historically, there has been an assumption of
performance deterioration when using recycled materials, and it was common prac-
tice for reprocessed plastics to be used in less demanding applications than virgin
polymers. However, improved understanding of polymer degradation has led to
closed-loop operation, where a product is recycled to make a very similar new prod-
uct. The supply of rPET is expected to increase with 2.1 million tonnes of recycled
material forecast to be available for 2017, compared to 1.7 million tonnes of PET
bottles recycled in 2012 (Plasteurope, 2013). The major market for rPET continues
to be fibres. Nonwovens made from rPET fibres are currently used in demanding
automotive applications, specifically: bonnet linings; boot floor coverings; cabin
insulation and wheel arch linings.
The melt processing of postconsumer waste is not limited to PET, and this process
can also be applied to PP, PE and poly(vinyl chloride) (PVC) products that can be
reprocessed in to pellets and fibres with ease. Alongside direct polymer-to-web pro-
duction, staple fibres produced from recycled products are readily available and are
commonly formed into nonwovens.
3.4.1 Cellulose II
Cellulose can be regenerated into textile fibres (Cellulose II) through the dissolution and
then precipitation into filaments. The viscose and the Lyocell process are the two main
104 Advances in Technical Nonwovens
10
8
6.73
6
3.61
4
1.62 1.67 1.94 2.04
2 1.49
0
2012 2013 2014 2015 2016 2017 2018 2020†
Recorded Forecast
Figure 3.1 Predicted increase in bioplastics production.
Aeschelmann, F., Carus, M., 2014. Bio-based Building Blocks and Polymers in the World:
Capacities, Production and Applications, Status Quo and Trends Towards 2020. Nova Institute,
Germany and yScion, 2014. Investment in Bioplastics Research Pays off, Press Release. Scion
Connections, United States.
routes in regenerating a cellulosic fibre, and the principle is essentially the same in both:
cellulose feedstocks from wood pulp are dissolved in an aggressive bath and chemically
altered to form a spinning dope. The solution is then spun into a precipitant bath and
then goes on to form either filament or staple fibres. Regenerated cellulosic fibres
have physical and chemical properties similar to cotton, and so, find uses where water
absorbency and close to skin comfort is desirable. Key applications for regenerated
cellulosic fibres are in the hygiene, wipes and incontinence sector. The technical appli-
cations for these products include fluid filters, automotive interior components and
medical swabs and wound dressings. These products are typically spunlaced but are
also processed using needle-punching and chemical bonding (Rodie, 2010).
The use of regenerated cellulosic fibres continues to grow, and annual consumption
increased by 9.6% to 5.8 million tonnes in 2013 from the previous year. In addition,
sales of Modal and Tencel fibres for nonwovens also increased by 13% in 2013
from 2012 (Lenzing, 2014). The use of these fibres in nonwoven materials is expected
to continue to grow in line with the general growth of the nonwoven industry. How-
ever, the price of man-made cellulosic fibres is intrinsically linked to the price of cot-
ton, a highly volatile commodity that brings in significant risks to any manufacturer
using such products (Mital, 2012).
Currently, the raw materials necessary for the renewable bio-PLA is typically sourced
from cornstarch that is grown solely for this purpose. Alternatives to cornstarch are being
explored, and Natureworks, a major PLA producer, has already moved to sourcing starch
from sugarcane in Thailand. The future possibility is that the process could be adapted to
use low-cost, high-volume lignocellulosics such as wood chips or wood grass to form
PLA that would significantly reduce the environmental impact and CO2 production.
The long-term goal is for Ingeo PLA to be sourced from a system that relies on the con-
version of CO2 or CH4 to lactic acid through a commercially viable chemical process.
Currently, PLA from cornstarch is seen as sustainable from a resource utilisation
point of view when compared to materials derived from oil-based feedstock (Vink
et al., 2003; Siede, 2014). In addition, the production and utilisation of PLA results
in lower greenhouse gas (GHG) emissions and environmental impact compared to
alternative polymers, Fig. 3.3. Future generations of PLA feedstock are forecast to
be GHG neutral or better due to the conversion of CO2 by the bio stock.
Ingeo PLA currently has an estimated cradle-to-gate GHG of 0.5e0.7 kg CO2/kg,
compared to 1.6e1.7 and 2e2.2 kg CO2/kg for PP and PET, respectively, depending
on production method and mode of calculation (Corbion Purac, 2013; Natureworks,
2009). In comparison to wool or cotton fibres, PLA requires significantly less water
and land for the production of an identical weight of fibres (Hagen, 2013). When com-
bined, these positive factors result in a highly sustainable polymer that has the potential
kg CO 2 per kg of polymer
0.0 1.0 2.0 3.0 4.0 5.0 6.0
PC 5.0
PS 2.2
PET 2
PP 1.7
LDPE 1.7
PLA 0.5
PLA† 0
to become a major component in the nonwoven industry. PLA is also readily processed
on existing PET staple and filament lines, often without modification, which has made
adoption of this biopolymer easier for nonwoven produces. However, the advantage in
using PLA comes at additional costs to the producer: currently, Ingeo PLA markets at a
price that is higher than fibre grade PET and fine cotton, and the tensile strength
is significantly lower than PET and nylon (Natureworks, 2006). A low melting
point (170 C) and low glass transition range (66e70 C) also limits the use of PLA
in applications where high temperatures are expected or possible in normal product
life (Solarski et al., 2005). However, a recent patent application for the use of PLA
nonwovens in tea and coffee bags suggests that for most domestic applications, the
PLA will meet the expected performance criteria (Foss and Turra, 2014).
The current range of applications for PLA nonwovens is extensive. Spunbond ma-
terial is currently produced by Fitesa, USA, for the use in feminine hygiene products
and as the top sheet in incontinence products. CL Nonwovens, China, are using PLA in
spunbonded nonwovens for use in agricultural, dust protection and packing materials.
Needle-punched PLA staple fibres are currently finding applications in mattress
wadding and in automotive carpeting. Crimped PLA staple fibre is also being blended
with wool to create high mattress toppers, which are made highly stable through ther-
mobonding the PLA component.
3.4.3 Chitosan
The examples given previously discussed biopolymers that were derived from terres-
trial plant biomass. This is not always the case, and biopolymers can be sourced from a
range of living matter. Chitosan is a polymer that is sourced from chitin, an abundant
material found in the exoskeletons of crustaceans and molluscs. Chitin is available in
large quantities as a by-product of the shrimp canning industry, comprising approxi-
mately 40% of shrimp processing waste. Much of this processing waste is dumped
in the sea, and so the reuse of this product has a direct ecological benefit by reducing
the volume of chitin released in to coastal environments (Arbia et al., 2013). Chitin is
extracted from crustacean matter and then deacetylated to form chitosan. Chitosan is
suitable for solution processing into fibres using suitable fibre spinning processes
and has acceptable mechanical and chemical performance for most applications
(Kumar, 1999). The unique biological properties of chitosan nonwovens has resulted
in applications in the wound care sector, but the decreasing cost of producing chitosan
has increased the volume of spunlaced disposable wipes and medical garments.
these materials as specific medical implants, and the ability to tailor the mechanical
performance and breakdown time has led to the design of specific materials for
different types of biological implants (Chen and Wu, 2005).
There has also been considerable effort in sourcing the materials needed for com-
modity polymers from renewable resources. Low-density polyethylene can also be
produced from a bioresource, namely, ethanol extracted from sugarcane. Brazilian
chemical company, Braskem, produce a branded product, I’m green polyethylene.
The production of this product is argued to be a net remover of CO2 from the atmo-
sphere (Ziem and Murphy, 2013). I’m green polyethylene is being incorporated in
to various nonwovens markets, including a range of hygiene products where the
bio-PE acts as a sheath to an Ingeo PLA core, an example of two biopolymers being
combined to blend the softness of PE with the robust strength of PLA (INDA, 2015).
Polymers part sourced from biological materials are also available: poly(trimethy-
lene terephthalate) (PTT) is produced by DuPont and trademarked as Sorona. This
polymer is produced from 1,3-propanedoil and terephthalic acid, the former being
formed from corn and the latter being derived from petroleum products (Kurian,
2005a). Sorona PTT is suitable for forming nonwovens through a range of processes
and combines the mechanical softness and drape of Nylon 6 with the chemical resil-
ience of PET (Kurian, 2005b). Whilst Sorona is not a 100% biopolymer, it represents
a significant step by large polymer manufacturers in moving the industry away from
purely petroleum-based materials and has been awarded biopreferred status by the
U.S. Department of Agriculture.
environmental impact of many products and endeavours. The use of a relatively low
weight of nonwoven agrotextiles and geotextiles can reduce the demand for other re-
sources, whether they are water, concrete, power or man hours, and the consumption of
these fabrics is expected to increase.
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