Title of Invention

A PROCESS FOR PRODUCING BIODIESEL FROM RENEWABLE OIL UNDER LIPASE CATALYSIS IN AN ORGANIC MEDIUM REACTION SYSTEM

Abstract The invention discloses a process for producing biodiesel from renewable oil under lipase catalysis in an organic medium reaction system, wherein a short chain alcohol ROH is used as an acyl acceptor, a relatively hydrophilic organic solvent having no negative effect on the reactivity of the lipase is used as a reaction medium, and a renewable oil raw material is catalyzed by a lipase to synthesize biodiesel through a transesterification reaction, characterized in that : the short chain alcohol and the renewable oil raw material having an alcohol/renewable oil molar ratio of 3:1 to 6:1, together with 20-200% by volume of the organic solvent based on the volume of the renewable oil, and 2-30% by weight of the lipase based on the weight of the renewable oil are added into an enzyme reactor and mixed evenly, the mixture is then heated to 20-60°C to react for 4-24 hours to convert the renewable oil raw material into biodiesel and byproduct glycerin, wherein said relatively hydrophilic organic solvent is selected from the group consisting of tert-butanol and short chain fatty acid ester RCOOR", wherein R and R' are independently an alkyl group having 1 to 4 carbon atoms.
Full Text TECHNICAL FIELD
The present invention relates to the field of bio-fuel synthesis, and
more particularly, relates to a new process for producing biodiesel from
renewable oil under lipase catalysis in an organic medium reaction
system.
BACKGROUND
As a promising material of renewable oil industry, biodiesel is a long
chain fatty acid ester produced from renewable oil through
rransesterification reaction. Biodiesel is a novel, pollutionless and
recoverable energy source. The combustion performance of biodiesel is
comparable with the conventional petroleum based diesel, while after
combustion, the content of harmful substances in the exhaust gas
decreases approximately by 50% as compared with the conventional
petroleum-based diesel. By far, wide attentions have been drawn to the
studies and applications regarding biodiesel.
Currently, biodiesel is manufactured mainly through chemical
methods. Particularly, vegetable oils and/or animal fats are used as a
source of long chain fatty acids and a transesterification reaction between
the long chain fatty acids and some short chain alcohols, such as
methanol or ethanol, is earned out in the presence of an acid or base
catalyst, and short chain ester of the fatty acids are obtained. However.
some inevitable disadvantages exist in chemical methods as follows::
(1). Free fatty acid and water contained in the renewable oil raw
material severely spoil the reaction;
(2). Emulsion is undesirably formed due to the poor solubility of
alcohol in renewable oils, and the subsequent treatment steps are
complicated;

(3). As required by the process, the amount of short chain alcohol
used is much more than the reaction molar ratio, and the
evaporation/reflux of the excess short chain alcohol leads to increased
energy consumption.
In contrast, synthesizing biodiesel through a biological enzyme
method has the following advantages: mild reaction conditions, non-toxic
emissions, and enzyme-catalyzed reactions am not affected by the free
fatty acid and small amount of water contained in the renev/able oil raw
materials. Therefore, bio-methods are consistent with the requirement of
developing Green Chemistry, and thus nave attracted more and more
attention,
However, when compared with the chemical process, there exist
some problems in the biological enzyme process. In an article entitled
Enzymatic alcoholysis for biodiesel fuel production and application of the
reaction to oil processing (Journal of Molecular Catalysis B: Enzymatic,
2002, 17: 133-142) written by Shimada Yuji et al„ it is reported that
firstly, the poor solubility of short chain alcofols, such as methanol and
ethanol, in the renewable oil raw material is unfavorable for the reaction;
and secondly, the presence of the excess alcohol may lead to severe
deactivation of the enzyme. Therefore, during the process of biodiesel
production by the biological enzyme method, batch addition of short
chain alcohol is generally adopted to moderate the poisonous effect
imposed on the enzyme. However, this process is complicated in
operation and needs long reaction time. Additionally, a short chain
alcohol is used as an acyl acceptor, and byproduct glycerin is produced
during the course of reaction, then the hydrophilic glycerin readily
adheres to the inner pores and the outer strface of the immobilized
enzyme forming a "shield" on the active sites of the enzyme, and severely
affecting the reactivity of the enzyme. Furthermore, the yield of biodiesel
synthesized by the enzyme process is relatively low compared with that
by the conventional chemical process. To solve above-mentioned
problems in a biological enzyme proce s, some scholars have tried to

produce biodiesel in organic solvent reaction svstem. It is reported in an
article entitled Enzymatic alcoholysis for biodiesel fuel production and
application of the reaction to oil processing (Journal of Molecular
Catalysis B: Enzymatic, 2002, 17: 133-142) written by Shimada Yuji et al
that, some relatively strong hydrophobic organic solvents, such as hexane,
cyclohexane and petroleum, ether can be used as reaction medium. These
hydrophobic solvents can dissolve renewable oil very well, thus
promoting the reaction to some extent. However, because these highly
hydrophobic solvents can not dissolve lower carbon alcohol, such as
methanol, as well as the byproduct glycerin effectively, the reactivity and
lifetime of the enzyme, and the yield of biodiesel can not be improved
notably.
SUMMARY OF THE INVENTION
Therefore, the object of the present invention is to provide a new
process for producing biodiesel from renewable oil raw material under
lipase catalysis in an organic medium reaction system. In this process, a
short chain alcohol ROH is used as an acyl acceptor, a relatively
hydrophilic organic solvent having no negative effect on the reactivity of
lipase is used as the reaction medium, and a renewable oil raw material is
catalyzed by a lipase to synthesize biodiesel through a transestenfication
reaction. The process of the present mvention is characterized in that: a
short chain alcohol and a renewable oil raw material having an
alcohol/renewable oil molar ratio of 3:1 to 6:1. together with 20 to 200%
by volume of an organic solvent based on the volume of the renewable oil,
and 2 to 30% by weight of a lipase based on the weight of the renewable
oil are added into an enzyme reactor and mixec evenly, and the mixture is
heated to 20 to 60'C to react for 4-24 hours tc convert the renewable oil
raw material into biodiesel and a byproduct glycerin.
BEST MODE OF THE INVENTION
In the process according to the present invention, said relatively
hydrophilic organic solvent is preferably selected from the group
consisting of tert-butanol and short chain farty acid ester RCOOR'.


wherein R and R' are independently an alkyl group having 1-4 carbon
atoms.
Said lipase is preferably a microorgamsm lipase, and is more
preferably selected from the group consisting Lipozyme TL, Lipozyme
RM, Novozym 435, and mixtures thereof.
Said renewable oil comprises biological renewable oils, and
preferably comprises vegetable oil, animal oil and fat, waste edible oil
and residues of refined oil.
Said vegetable oil comprises castor oil, rapeseed oil, soybean oil,
peanut oil, corn oil, cottonseed oil, rice oil, algae oil and mixtures thereof.
Said animal oil and fat comprise fish oil, lard and mixture thereof.
In said short chain alcohol ROH, R is an a kyl group having 1 to 5
carbon atoms, and preferably said short chain alcohol comprises methanol,
ethanol, propanol, butanol and pentanol.
Preferably, the reaction molar ratio of said short chain alcohol to
said renewable oil is 3:1 to 5:1, and the amount of the organic solvent
added is 50% to 100% by volume based on the volume of the renewable
oil.
Said enzyme reactor may be a triangle fla;k with a plug, or other
suitable enzyme reactors. Preferably, the heating step is carried out in an
automatically thermostatic oscillating shaker or in various other
bio-reactors suitable for enzyme catalyzed leaction. The preferred
temperature for the reaction is 30 to 50°C.
The advantages of the process of the present invention comprise the
improvement of the lipase reactivity, prolongation of the lifetime of the
lipase, and remarkable increase in the yield of biodiesel. This new


organic medium reaction system promotes the solubility of the short
chain alcohol in the renewable oil raw material, and effectively decrease
the negative influence imposed on the lipase reactivity by the short chain
alcohol. In the organic medium reaction system, the desired short chain
alcohol may be added in one step to shorten the reaction time notably,
and the yield of biodiesel is increased to 94% or more. Furthermore, the
relatively hydrophilic organic solvent dissolves part of the byproduct
glycerin and thus the "shield" effect imposed on the immobilized lipase
pores by glycerin is avoided, and the lipase reactivity and lifetime are
improved.
The present invention is further illustrated by the following
examples.
Example 1
Into a triangle flask with a plug, methaol and rapeseed oil in a
molar rario of 4:1 (9.65g rapeseed oil) together with 100% by volume of
tert-butanol based on the volume of the rapeseed oil were added and
mixed evenly, the flask was placed in an automatically thermostatic
oscillating shaker, and the mixture was heated to 40oC, then 10% by
weight of a immobilized lipase Novozym 435 based on the weight of the
rapeseed oil was added to start reaction, and the reaction was carried out
for 6 hours. 9.64g biodiesel was produced with £n yield of about 100%.
Example 2
Into a triangle flask with a plug, methanol and soybean oil in a molar
ratio of 3:1 (9.65g soybean oil) together w th 20% by volume of
tert-butanol based on the volume of the soybean oil were added and
mixed evenly, the flask was placed in an automatically thermostatic
oscillating shaker, and the mixture was heatei to 20°C, then 2% by
weight of immobilized lipase Novozym 435 ba;ed on the weight of the
soybean oil was added to start reaction, and the reaction was carried out
for 24 hours. 9.17g biodiesel was produced with an yield of 95%.


Example 3
Into a triangle flask with a plug, ethanol and cottonseed oil in a
molar ratio of 5:1 (9.65g cottonseed oil) togethe- with 200% by volume
of methyl formate based on the volume of the ccttonseed oil were added
and mixed evenly, the flask was placed in an automatically thermostatic
oscillating shaker, and the mixture was heated to 60oC, then 10% by
weight of immobilized lipase Novozym 435 based on the weight of the
cottonseed oil was added to start reaction, and he reaction was carried
out for 12 hours. 9.1g biodiesel was produced with an yield of 94%.
Example 4
Into a triangle flask with a plug, butanol and waste edible oil in a
molar ratio of 3:1 (9.65g waste edible oil) together with 80% by volume
of tert-butanol based on the volume of the waste edible oil were added
and mixed evenly, the flask was placed in an automatically thermostatic
oscillating shaker, and the mixture was heated to 40°C, then 10% by
weight of immobilized lipase Novozym 435 based on the weight of the
waste edible oil was added to start reaction, and the reaction was carried
out for 7 hours. 9.65g biodiesel was produced wi :h an yield of 100%.
Example 5
Into a triangle flask with a plug, methanol and soybean oil in a molar
ratio of 3:1 (9.65g soybean oil) together with 50%o by volume of
tert-butanol based on the volume of the soybean oil were added and
mixed evenly, the flask was placed in an automatically thermostatic
oscillating shaker, and the mixture was heated to 40°C, then 20% by
weight of immobilized lipase Lipozyme TL based on the weight of the
soybean oil was added to start reaction, and the reaction was carned out
for 10 hours. 9.1g biodiesel was produced with an yield of 94%.
Example 6
Into a triangle flask with a plug, pentanol ar d rapeseed oil in a molar
ratio of 4:1 (9.65g rapeseed oil) together with 100% by volume of butyl
butyrate based on the volume of the rapeseed o .1 were added and mixed


evenly, the flask was placed in an automatically thermostatic oscillating
shaker, and the mixture was heated to 50oC, hen 30% by weight of
immobilized lipase Lipozyme TL based on the weight of the rapeseed oil
was added to start reaction, and the reaction was carried out for 8 hours
9.17g biodiesel was produced with an yield of 95%.
Example 7
Into a triangle flask with a plug, ethanol and cottonseed oil in a
molar ratio of 3:1 (9.65g cottonseed oil) together with 80% by volume of
tert-butanol based on the volume of the cotton; eed oil were added and
mixed evenly, the flask was placed in an automatically thermostatic
oscillating shaker, and the mixture was heated to 40 °C, then 20% by
weight of immobilized lipase Lipozyme RM based on the weight of the
cottonseed oil was added to start reaction, and the reaction was carried
out for 10 hours. 9.1 g biodiesel was produced with an yield of 94%.
Example 8
The lipase remained after the reaction of example 1 was filtered and
used in the next reaction batch, while other read ion conditions were kept
as same as those in example 1, and the lipase was used repeatedly 10
times in the same way. During the 10th reaction batch, 9.62g biodiesel
was produced with an yield of 99% after 6 hours of reaction.
According to the above-mentioned example s, when tert-butanol or a
short chain fatty acid ester RCOOR' (wherein R and R' are independently
an alkyl group having 1 to 4 carbon atoms) is used as an organic mediurrL
and a short chain alcohol ROH (wherein R is an alkyl group having 1 to 5
carbon atoms) is used as an acyl acceptor, various renewable oil raw
materials (castor oil, rapeseed oil, cottonseed oil, waste edible oil,
soybean oil, fish oil, lard, residues of refined oil and algae oil, etc.) can be
converted into biodiesel effectively under a suitable temperature
condition upon the addition of 2 to 30% by weight based on the weight of
the renewable oil of an immobilized lipase, such as Novozym 435
(available from Candida antarctica), Lipozyme RM (available from


Rhizomucor miehei) and Lipozyme TL (available from Thermomyces
lanuginosus).

WE CLAIM:
1. A process for producing biodiesel from renewable oil under lipase catalysis in
an organic medium reaction system, wherein a short chain alcohol ROH is used as an
acyl acceptor, a relatively hydrophilic organic solvent having no negative effect on the
reactivity of the lipase is used as a reaction medium, and a renewable oil raw material
is catalyzed by a lipase to synthesize biodiesel through a transesterification reaction,
characterized in that:
the short chain alcohol and the renewable oil raw material having an
alcohol/renewable oil molar ratio of 3:1 to 6:1, together with 20-200% by volume of
the organic solvent based on the volume of the renewable oil, and 2-30% by weight of
the lipase based on the weight of the renewable oil are added into an enzyme reactor
and mixed evenly, the mixture is then heated to 20-60°C to react for 4-24 hours to
convert the renewable oil raw material into biodiesel and byproduct glycerin, wherein
said relatively hydrophilic organic solvent is selected from the group consisting of
tert-butanol and short chain fatty acid ester RCOOR', wherein R and R' are
independently an alkyl group having 1 to 4 carbon atoms.
2. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 1, wherein:
said lipase is a microorganism lipase.
3. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 2, wherein:
said microorganism lipase comprises Lipozyme TL, Lipozyme RM, Novozym
435 or mixtures thereof.
4. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 1, wherein:


said renewable oil is a biological renewable oil.
5. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 4, wherein:
said biological renewable oil comprises vegetable renewable oil, animal
renewable oil, waste edible oil or residues of refined oil.
6. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 5, wherein:
said vegetable renewable oil comprises castor oil, rapeseed oil, soybean oil,
peanut oil, corn oil, cottonseed oil, rice oil, algae oil or mixtures thereof.
7. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 5, wherein:
said animal renewable oil comprises fish oil, lard or mixture thereof.
8. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 1, wherein:
in said short chain alcohol ROH, R is an alkyl group having 1 to 5 carbon
atoms.
9. The process for producing biodiesel from renewable oil under lipase catalysis
in an organic medium reaction system as claimed in claim 8, wherein:
said short chain alcohol is selected from the group consisting of methanol,
ethanol, propanol, butanol and pentanol.
10. The process for producing biodiesel from renewable oil under lipase
catalysis in an organic medium reaction system as claimed in claim 1, wherein:
the molar ratio of said short chain alcohol to said renewable oil is 3:1 to 5:1.


11. The process for producing biodiesel from renewable oil under lipase
catalysis in an organic medium reaction system as claimed in claim 1, wherein:
the amount of said organic solvent added is 50% to 100% by volume based on
the volume of the renewable oil.
12. The process for producing biodiesel from renewable oil under lipase
catalysis in an organic medium reaction system as claimed in claim 1, wherein:
the heating step is carried out in an automatically thermostatic oscillating
shaker.
13. The process for producing biodiesel from renewable oil under lipase
catalysis in an organic medium reaction system as claimed in claim 1, wherein:
the reaction temperature is in the range of 30°C to 50°C.


The invention discloses a process for producing biodiesel from renewable oil under
lipase catalysis in an organic medium reaction system, wherein a short chain alcohol
ROH is used as an acyl acceptor, a relatively hydrophilic organic solvent having no
negative effect on the reactivity of the lipase is used as a reaction medium, and a
renewable oil raw material is catalyzed by a lipase to synthesize biodiesel through a
transesterification reaction, characterized in that : the short chain alcohol and the
renewable oil raw material having an alcohol/renewable oil molar ratio of 3:1 to 6:1,
together with 20-200% by volume of the organic solvent based on the volume of the
renewable oil, and 2-30% by weight of the lipase based on the weight of the
renewable oil are added into an enzyme reactor and mixed evenly, the mixture is then
heated to 20-60°C to react for 4-24 hours to convert the renewable oil raw material
into biodiesel and byproduct glycerin, wherein said relatively hydrophilic organic
solvent is selected from the group consisting of tert-butanol and short chain fatty acid
ester RCOOR", wherein R and R' are independently an alkyl group having 1 to 4
carbon atoms.

Documents:

02095-kolnp-2006 abstract.pdf

02095-kolnp-2006 claims.pdf

02095-kolnp-2006 correspondence others.pdf

02095-kolnp-2006 description(complete).pdf

02095-kolnp-2006 form-1.pdf

02095-kolnp-2006 form-3.pdf

02095-kolnp-2006 form-5.pdf

02095-kolnp-2006 gpa.pdf

02095-kolnp-2006 international publication.pdf

02095-kolnp-2006 international search authority report.pdf

02095-kolnp-2006 pct others document.pdf

02095-kolnp-2006 priority document.pdf

2095-kolnp-2006-assignment.pdf

2095-KOLNP-2006-CORRESPONDENCE.pdf

2095-kolnp-2006-correspondence1.1.pdf

2095-kolnp-2006-CORRESPONDENCE1.2.pdf

2095-kolnp-2006-examination report.pdf

2095-kolnp-2006-form 18.pdf

2095-kolnp-2006-form 3.pdf

2095-kolnp-2006-form 5.pdf

2095-kolnp-2006-gpa.pdf

2095-kolnp-2006-granted-abstract.pdf

2095-kolnp-2006-granted-claims.pdf

2095-kolnp-2006-granted-description (complete).pdf

2095-kolnp-2006-granted-form 1.pdf

2095-kolnp-2006-granted-form 2.pdf

2095-kolnp-2006-granted-specification.pdf

2095-KOLNP-2006-OTHERS.pdf

2095-kolnp-2006-others1.1.pdf

2095-kolnp-2006-reply to examination report.pdf


Patent Number 250565
Indian Patent Application Number 2095/KOLNP/2006
PG Journal Number 02/2012
Publication Date 13-Jan-2012
Grant Date 10-Jan-2012
Date of Filing 25-Jul-2006
Name of Patentee TSINGHUA UNIVERSITY
Applicant Address QINGHUAYUAN, HAIDIAN DISTRICT, MAILBOX 82, BEIJING, 100084, CHINA
Inventors:
# Inventor's Name Inventor's Address
1 DU, WEI QINGHUAYUAN, HAIDIAN DISTRICT, MAILBOX 82, BEIJING, 100084, CHINA
2 LI, LILIN QINGHUAYUAN, HAIDIAN DISTRICT, MAILBOX 82, BEIJING, 100084, CHINA
3 XU, YUANYUAN QINGHUAYUAN, HAIDIAN DISTRICT, MAILBOX 82, BEIJING, 100084, CHINA
4 WANG, LI QINGHUAYUAN, HAIDIAN DISTRICT, MAILBOX 82, BEIJING, 100084, CHINA
5 LIU, DEHUA QINGHUAYUAN, HAIDIAN DISTRICT, MAILBOX 82, BEIJING, 100084, CHINA
PCT International Classification Number C11C 3/10
PCT International Application Number PCT/CN2004/001372
PCT International Filing date 2004-11-29
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 200410000697.9 2004-01-16 China