Professional Documents
Culture Documents
A Brief History of Bioplastics
A Brief History of Bioplastics
The term “bioplastics” seems to cause almost as much confusion as the term “biodegradable.”
So what are bioplastics—and what, exactly, does the “bio” in bioplastics refer to?
Bio … bio … hmmm. The history of plastics? No. Biotechnology? No. The “bio” in
bioplastics actually has more to do with that oft-dreaded high school class, biology. You
know: having to do with life, living organisms, biological systems and the like.
Ok… biological organism and plastics. Since oil and natural gas originate from biological
organisms, does that mean plastics derived from oil and natural gas are bioplastics? Well, not
really—at least that’s not how the term is commonly used. So just what are bioplastics?
Let’s step back in time for a bit of perspective. The very first plastics were (and still are)
made by plants through their very own internal chemical synthesis. Rubber from a rubber
tree, for example, is actually a plastic. Early synthetic or “manmade” plastics were largely an
One of the first synthetic plastics was made from cellulose, a substance made by plants and
trees. In today’s vernacular, this plastic is deemed a bioplastic. That means its primary raw
materials (feedstocks) originate from “biomass:” living or recently living and renewable bio-
Early bioplastics were largely eclipsed by more efficient plastics. The raw materials for
today’s plastics come from many places (some even use salt), but most plastics can be made
from the hydrocarbons that are readily available in natural gas, oil and coal. Even though
these resources are derived from living organisms, they are not alive, recently alive or
renewable (biomass). So plastics made from natural gas, oil or coal are not considered
bioplastics.
Interest in bioplastics and other “bio” products has been growing (get it?) due to concern
about the use of finite resources, primarily natural gas and oil. Bioplastics are reemerging
today as scientists develop more efficient ways to produce the necessary quantities of
Bioplastics ≠ Biodegradable
also be biodegradable. However, the use of “bio” feedstocks does not necessarily mean that
For example, a bioplastic called polylactic acid (PLA) is made with plant feedstocks and is
considered biodegradable in a commercial composting facility. But PET bioplastic made with
plant feedstocks is not biodegradable. In other words, the “bio” in bioplastics does not mean
biodegradable.
LITERATURE REVIEW
According to the „Oxford Dictionary‟ word „Plastic‟ was coined in the mid of 17th century
and derived from French „plastique’, Latin „plasticus’ or from Greek „plastikos’/ „plassein’.
Meaning of all these cognates is „able to be molded into different shapes‟ (Joel, 1995). The
first man-made plastic, a modification of cellulose, was created by Alexander Parkes in 1862
and called „Parkesine‟. In 1868 John Wesley Hyatt invented Celluloid, derived from
cellulose and alcoholized camphor that could be molded with heat and pressure into a durable
shape. By 1900, movie film was an exploding market for celluloid (Harris, 1981).
Plastic, from the time of their origin have become an indispensable part of our life and in
modern society. Synthetic plastics are extensively used in packaging of products like food,
pharmaceuticals, cosmetics, detergents and many products manufactured from plastics are a
boon to public health, e g. disposable syringes and intravenous bags (Halden, 2010). This
utilization is still expanding at a high rate of 12% per annum (Sabir, 2004) and has replaced
paper and other cellulose-based products for packaging because of their better physical and
chemical properties viz. strength, lightness, resistance to microorganisms (Shah et al., 2008)
and favorable mechanical/thermal properties, stability and durability (Rivard et al., 1995).
With time, stability and durability of plastics have been improved continuously, hence this
group of materials is now considered as a synonym for the materials being resistant to many
environmental influences (Joel, 1995). Plastic is inert i.e. resistant to biodegradation, durable,
hygienic, lightweight, cheap, and malleable (Mohee and Unmar, 2007). It has been proven
that polyolefins especially low density polyethylene (LDPE), are resistant against degradation
span of one year (1996-95) shipments from the Canadian Plastic Industry increased by 10.6%
(Charron, 2001). In Australia about 1 million tones of plastic materials are produced each
year and a further 587,000 tonnes are imported (Australian Academy of Science, 2002). In
European countries on an average 100kg of plastic is used per person each year (Mulder,
1998.) The bags, with a typical thickness of 16 microns and weight of 7-8 gm are provided
free of charge in Israeli stores and supermarkets (Ayalon et al., 2009). In Mauritius, plastic
wastes constitute around 8% by weight (or 100 tonnes) of the total solid waste generated
daily. The amount of plastic carry-bags disposed at the landfill is approximately 1000 tonnes
annually, while the local plastic industries generate around 250–300 million plastic carry
bags per annum (Mohee and Unmar, 2007). In Israel, 2 billion HDPE carrier bags are
manufactured every year. The total amount of these bags is 30,000 tons/year. At the end of
2007, there were 2,007,300 households in Israel. It means that the consumption in Israel per
household is 1000 bags /yr, 2.7 bags per day. Every person in Israel uses an average of 300
bags /yr, similar to other countries such as Ireland, where before introduction of the levy, a
yearly average was of 330 bags per person (Ayalon et al., 2009). The estimated figure of
plastic waste generation across the Pakistan was 1.32 million tons per annum (Sabir, 2004).
The plastic industry in Pakistan was reported to be growing at an average annual growth rate
Extraction of cellulose from pulp: Cellulose is extracted from paper sludge after treating it
hemicellulose fraction. Both of these exhibited high levels of purity, without any yield
called Cellulolysis. Cellulolysis is the process of breaking down cellulose into smaller
reaction. Because cellulose molecules bind strongly to each other, cellulolysis is relatively
can be significantly intensified in a proper solvent, e.g. in an ionic liquid. The enzymes
utilized to cleave the glycosidic linkage in cellulose are glycoside hydrolases including
endo-acting cellulases and exo-acting glucosidases. Such enzymes are usually secreted as
part of multi enzyme complexes that may include dockerins and carbohydrate-binding
modules.
The present invention relates to a process for the production of glucose from cellulose.
In one of its more specific aspects, this invention relates to a process for the conversion of
derived from Aspergillus terreus. In another of its more specific aspects, this invention
relates to a process for the production of a purified enzyme having a very high
activity for the production of glucose from cellobiose. There is presently tremendous
scientific and commercial activity in the quest for economic means to convert cellulose
(abundant in the form of wood, waste paper, and agricultural products, e.g. bagasse) to
glucose and thence to ethanol and other chemicals. Cellulose may be converted to glucose
by the action of various enzymes derived from molds. It is known from the prior art that
Trichoderma reesei is a fungus that has the ability to degrade cellulose very rapidly.
Currently Trichoderma reesei is the preferred orgnaism for studies in the hydrolysis of
cellulose to glucose for industrial purposes. The conversion of cellulose to glucose is not
yet economically feasible, due partially to the fact that the cellobiase produced by
Trichoderma reesei has a low specific activity. Additionally, glucose, which is the
final product of reaction, further inhibits the activity of the Trichoderma reesei enzymes. We
have discovered an efficient method for the conversion of cellulose to glucose in a two
stage process. In the first stage, cellulose is converted to cellobiose by the action of a
This is a distinct departure from the prior art processes in which Trichoderma reesei
enzymes perform both functions at efficiencies and conversion rates considerably less
than those obtained in our process. 3. Preparation of PLA bio-plastic: To produce PLA,
starch is extruded from waste newspaper, which results in a simple starch called
dextrose. Dextrose is a type of glucose, which is a simple sugar that plants produce during
photosynthesis. Now dextrose is put through a fermentation process similar to the one
used to make beer. Instead of alcohol, however, the dextrose is converted into lactic acid --
the same stuff that makes your muscles cramp when you exercise without proper
hydration. Heat is applied to the lactic acid polymers, causing them to link together and
form a long chain that ultimately becomes the material used to make many bio-plastic
products.
CONCLUSIONS
The environmentally benign natural cellulose-based CA either from flax fibers or cotton
linters was prepared successfully by using sulfuric acid–catalyzed acetylation process and
was found that CA produced as viscous acetone–soluble fluid and the production yield of CA
from flax fibers (81%) was higher than that from cotton linters (54%). In addition, it was
better than that from cotton linters in terms of biodegradation properties (41–44% weight loss
after 14 days) but they had nearly the same chemical resistance. Also, the produced CA
proved to be comparable with polyethylene and polypropylene with respect to its resistance
to 30% sulfuric acid and 40% NaOH. Flax fiber is recommended for the commercial
production of CA because of its higher production yield and it is available in large quantities
compared with cotton linters; these are used as an ingredient of cattle feed. This acceptable
overall performance, shown by this CA, has put it forward as a suitable material for packages,
salt containers, fiber and plastic tools manufacture. This CA has the potential to replace or
Alexander
Germany
Arabic, 2012
Arantadesign, 2014
Arg-egypt, 2011
ASTM D5988-12, 2012. Standard test method for determining aerobic biodegradation
Axel, 2009
S. Axel