WO2000036056A1 - Gasification of biosludge - Google Patents

Gasification of biosludge Download PDF

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Publication number
WO2000036056A1
WO2000036056A1 PCT/US1999/028617 US9928617W WO0036056A1 WO 2000036056 A1 WO2000036056 A1 WO 2000036056A1 US 9928617 W US9928617 W US 9928617W WO 0036056 A1 WO0036056 A1 WO 0036056A1
Authority
WO
WIPO (PCT)
Prior art keywords
biosludge
oil
water
hot
intracellular water
Prior art date
Application number
PCT/US1999/028617
Other languages
French (fr)
Inventor
John Duckett Winter
George Neal Richter
Original Assignee
Texaco Development Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Texaco Development Corporation filed Critical Texaco Development Corporation
Priority to CA 2348787 priority Critical patent/CA2348787C/en
Priority to JP2000588308A priority patent/JP3849047B2/en
Priority to AU21634/00A priority patent/AU745358B2/en
Priority to EP99965975A priority patent/EP1141177B1/en
Priority to DE1999635251 priority patent/DE69935251T2/en
Priority to US09/807,267 priority patent/US6436157B1/en
Publication of WO2000036056A1 publication Critical patent/WO2000036056A1/en

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Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F26DRYING
    • F26BDRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
    • F26B5/00Drying solid materials or objects by processes not involving the application of heat
    • F26B5/04Drying solid materials or objects by processes not involving the application of heat by evaporation or sublimation of moisture under reduced pressure, e.g. in a vacuum
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L5/00Solid fuels
    • C10L5/40Solid fuels essentially based on materials of non-mineral origin
    • C10L5/46Solid fuels essentially based on materials of non-mineral origin on sewage, house, or town refuse
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0903Feed preparation
    • C10J2300/0909Drying
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/16Integration of gasification processes with another plant or parts within the plant
    • C10J2300/1681Integration of gasification processes with another plant or parts within the plant with biological plants, e.g. involving bacteria, algae, fungi
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/1846Partial oxidation, i.e. injection of air or oxygen only
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or diesel

Definitions

  • Wastewater treatment facilities separate the wastewater components
  • Sewage sludge is a mixture of
  • Wastewater is generally subjected to a primary treatment wherein the
  • suspended solid content is removed by physical means such as screening and
  • microorganisms primarily bacteria
  • the mixture of microorganisms is usually referred to as
  • biomass During the biological treatment of wastewater or sewage, the
  • waste components function as nutrients for the microorganisms, enabling
  • the wasted microorganisms are referred to as
  • biosludge A major cost component of all biologically based processes is
  • the first step in sludge processing is often concentration, by such
  • Organic sludges from primary treatment can usually be concentrated
  • Biosludge is the organic biomass remaining after biological waste
  • Biosludge usually has to be mechanically dewatered to
  • source of water in the biosludge is contained within the cells of biota present
  • biosludge filter cake with no free liquid can still have a water content in
  • liquid is liquid that is not physically adsorbed or encumbered or chemically
  • biosludge and utilizing the biosludge are costly and require excessive
  • the bacterial cells of a dewatered biosludge is reduced by removing the
  • This operation comprises
  • the weakened cell walls are then exposed to a reduced pressure
  • FIG 1 is a simplified schematic representation of the biosludge
  • the biosludge is
  • the partial oxidation gasification reaction is conducted under reaction
  • reaction temperatures typically range from about 900°C to
  • the average residence time in the reaction zone generally is the average residence time in the reaction zone.
  • Non- gaseous byproducts include parti culate materials, generally
  • hydrocarbonaceous fuel and introduced into the partial oxidation reactor for the production of syngas. It is important to maximize the ratio of the
  • the fuel loading can be
  • the water content of the biosludge decreases and the solids content increases.
  • weight basis is about 1 :50 to about 1 : 1, and preferably about 1 :25 to about
  • the biosludge or biosolids fed to the dewatering process can be at any combination
  • the biosludge can be sourced from the material
  • biosludge feed to the dewatering process containing greater than 3% by
  • the biosludge feed is preheated
  • syngas cooler flashgas condenser, or quench water coolers.
  • a particularly desirable source of heat for the preheating step is the water vapor exiting the
  • the biosludge feed material with or without preheating by heat
  • biosludge evaporator is typically a flash evaporator.
  • biosludge evaporator varies from about 1 : 1 to about 20: 1, and preferably
  • the temperature and pressure of the contacting step is regulated so
  • the hot oil and biosludge enter the evaporator through a pressure
  • the pressure reducing device is typically a valve located on the exterior inlet to the evaporator.
  • the cell structure housing the intracellular water is weakened.
  • Suitable pressures in the evaporator vary from about 0 to about 60
  • biosludge/oil mixture prior to the pressure reduction step are about 80°C to
  • a separate stream of hot oil can be
  • the hot oil and concentrated biosludge mixture provide
  • the overhead vapor from the evaporator can be cooled by heat
  • water condensed from the vapor can be used as a moderator in the partial
  • Excess water can be routed to a wastewater
  • the reboiler can be heated with external steam or fuel or can use
  • gasification system includes syngas trim coolers, syngas coolers, flashgas
  • biosludge stream 2 enters the heat exchanger
  • Cooled water vapor stream 10 which can also be a mixture of liquid
  • heat exchanger 4 exits heat exchanger 4 at a temperature of about 25°C to about
  • Heated biosludge stream 16 exits the heat exchanger 4 at a temperature
  • the hot oil stream 18 also contains a portion 30 of concentrated
  • the pressure is typically below the saturation pressure of water at the temperature of stream 22, for example, about 0.01 atmospheres
  • the pressure can vary from about 0.1 atmospheres (1.47 psia) to
  • the hot oil stream 18 can be any oil with a heating value above about
  • Typical examples of suitable oils include heavy crude
  • the biosludge evaporator 8 operates at conditions which are designed
  • biosludge evaporator 8 is divided into oil/sludge streams 25 and 30.
  • Supplemental oil feed 26 from reservoir 40 can be combined as needed with
  • the additional oil feed stream 42 from oil feed reservoir 40 can be any oil feed stream 42 from oil feed reservoir 40.
  • in streams 27 and 42 varies from about 0.01 : 1 to about 1 : 1, and preferably
  • the reboiler 20 can be heated with steam, flashgas, or hot water, or
  • the sources of heat used will depend on the ratio of biosludge to oil
  • the concentrated biosludge/oil mixture is divided into
  • combination is heated to 350°C and combined with incoming biosludge.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Treatment Of Sludge (AREA)
  • Processing Of Solid Wastes (AREA)

Abstract

The high intracellular water content contained within the cell walls of the bacterial cells of a dewatered biosludge is reduced by removing the intracellular water in a denaturing operation. This operation comprises heating the biosludge (2) at a temperature (4) sufficient to weaken the bacterial cell walls. The weakened cell walls are then exposed to a reduced pressure (8) sufficient to form vapor within the cell and to thus rupture the weakened cell walls and thereby release the intracellular water. The water-reduced concentrated biosludge (24) can then serve as a fuel source in a partial oxidation reaction for the production of synthesis gas.

Description

GASIFICATION OF BIOSLUDGE
BACKGROUND OF THE INVENTION
Wastewater treatment facilities separate the wastewater components
into coarse solids, scum grit and sludge. Sewage sludge is a mixture of
suspended, colloidal and dissolved organic and inorganic matter which is
separated from wastewater during treatment.
Wastewater is generally subjected to a primary treatment wherein the
suspended solid content is removed by physical means such as screening and
gravity sedimentation. Chemical precipitation is useful in removing
lightweight suspended and colloidal solids.
The remaining liquid sewage is then subjected to a secondary
treatment wherein microorganisms, primarily bacteria, are used to stabilize
and denature waste components by degrading complex organics and/or
killing pathogens. The mixture of microorganisms is usually referred to as
"biomass." During the biological treatment of wastewater or sewage, the
waste components function as nutrients for the microorganisms, enabling
them to reproduce and multiply as they stabilize and denature the waste
components.
Thus, the quantity of biomass in a waste treatment system increases
during the stabilization and denaturing treatment. In order to avoid the
buildup of an excessive amount of microorganisms which can "choke" the process, a portion of the microorganisms must be removed or "wasted" from
the treatment system. The wasted microorganisms are referred to as
"biosludge." A major cost component of all biologically based processes is
the need to dispose of this biosludge in an environmentally acceptable
fashion.
The general treatment or management of sludge involves stabilization
of biodegradable organics, concentration and dewatering, and ultimate
disposal of the stabilized, dewatered residue.
Generated sludges are often dilute, on the order of about 1 -2 percent
solids by weight. In order to reduce the volumetric loading on other
processes, the first step in sludge processing is often concentration, by such
means as gravity thickening and flotation.
Organic sludges from primary treatment can usually be concentrated
to about 5-8 weight percent solids. Sludges from secondary treatment can
usually be gravity thickened to about 2 to 4 weight percent solids.
Dewatering is different from concentration in that concentration still
leaves the sludge with the properties of a liquid. Dewatering uses
mechanical operations such as centrifugation, vacuum and/or pressure
filtration and sand beds to produce a product which is essentially a friable
solid. When the water content of sludge is reduced by dewatering to about
65-80 percent, it forms a porous solid called sludge cake. There is no free water in the cake as the water is chemically combined with the solids or
tightly adsorbed on the internal pores or held within the cells of
microorganisms.
Biosludge is the organic biomass remaining after biological waste
water treatment. Biosludge usually has to be mechanically dewatered to
reduce water content below approximately 96 weight %. A significant
source of water in the biosludge is contained within the cells of biota present
in the sludge, and is referred to as "intracellular water." A dewatered
biosludge filter cake with no free liquid can still have a water content in
excess of 80% by weight due principally to the amount of intracellular water
contained in the cells of the dewatered biosludge.
"Dry solids" is the water-free residue left after a sample is dried in
nitrogen at 105°C until no further weight loss is observed. The term "free
liquid" is liquid that is not physically adsorbed or encumbered or chemically
combined, and can be released through conventional filtration processes.
Currently available technologies for reducing the water content of the
biosludge and utilizing the biosludge are costly and require excessive
amounts of energy. In particular, they have all been found to be
uneconomical and impractical means for converting biosludge and sewage
sludge into a viable feed for a partial oxidation gasification reaction. SUMMARY OF THE INVENTION
The high intracellular water content contained within the cell walls of
the bacterial cells of a dewatered biosludge is reduced by removing the
intracellular water in a denaturing operation. This operation comprises
heating the biosludge at a temperature sufficient to weaken the bacterial cell
walls. The weakened cell walls are then exposed to a reduced pressure
sufficient to form vapor within the cell and to thus rupture the weakened cell
walls and thereby release the intracellular water as free water or in the form
of a hot aqueous vapor. The water-reduced concentrated biosludge can then
serve as a fuel source in a partial oxidation reaction for the production of
synthesis gas.
BRIEF DESCRIPTION OF THE DRAWING
FIG 1 is a simplified schematic representation of the biosludge
concentration treatment.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
In accordance with the present invention the heat values contained in
biosludge can be used as a simple and effective fuel source in a partial
oxidation process for the production of synthesis gas. The biosludge is
usually combined with a supplemental hydrocarbonaceous fuel such as coal or oil, and undergoes cogasification in a partial oxidation reaction to
generate synthesis gas, also referred to as "syngas".
The partial oxidation gasification reaction is conducted under reaction
conditions that are sufficient to convert a desired amount of fuel or feedstock
to synthesis gas. Reaction temperatures typically range from about 900°C to
about 2,000°C, preferably from about 1,200°C to about 1,500°C. Pressures
typically range from about 1 to about 250 atmospheres, preferably from
about 10 to about 200 atmospheres and most preferably about 20 to 80
atmospheres. The average residence time in the reaction zone generally
ranges from about 0.5 to about 20, and preferably from about 1 to about 10
seconds.
The syngas reaction product leaving the partial oxidation reactor
generally includes CO, H2, steam, CO2, H2S, COS, CH4, NH3, N2, volatile
metals and inert gases such as argon. The specific product composition will
vary depending upon the composition of the feedstock and the reaction
conditions. Non- gaseous byproducts include parti culate materials, generally
carbon and inorganic ash.
The efficiency and economic viability of the biosludge cogasification
process requires the solids content of the biosludge be increased to as high a
level as possible before being combined with the supplemental
hydrocarbonaceous fuel and introduced into the partial oxidation reactor for the production of syngas. It is important to maximize the ratio of the
biosludge to the supplemental fuel. Otherwise, the fuel loading can be
hindered by the high water content and/or poor slurrying properties of the
biosludge. Thus, the efficiency of the gasification of biosludge increases as
the water content of the biosludge decreases and the solids content increases.
A suitable ratio of biosludge to hydrocarbonaceous fuel on a water-free
weight basis is about 1 :50 to about 1 : 1, and preferably about 1 :25 to about
1 :2, respectively.
The biosludge or biosolids fed to the dewatering process can be at any
water content. Thus, the biosludge can be sourced from the material
produced by simple settling in a primary treatment facility, or from
mechanically dewatered feed, and the like. The initial water content will
influence the amount of water removed in relation to the amount of "dry"
solids produced and the size of the heat exchangers. It is preferred to use a
biosludge feed to the dewatering process containing greater than 3% by
weight dry solids.
In one embodiment of the invention, the biosludge feed is preheated
by heat exchange with a heat source prior to the evaporation step. Generally
there will be large amounts of low grade excess heat available for heat
exchange from the syngas cooling train comprising the syngas trim cooler,
syngas cooler, flashgas condenser, or quench water coolers. A particularly desirable source of heat for the preheating step is the water vapor exiting the
biosludge evaporator.
The biosludge feed material, with or without preheating by heat
exchange with the water vapor exiting the biosludge evaporator, is combined
with a hot oil stream exiting the reboiler of a biosludge evaporator. The
biosludge evaporator is typically a flash evaporator. The relative amount of
hot oil to biosludge on an as-fed basis in the combined stream to the
biosludge evaporator varies from about 1 : 1 to about 20: 1, and preferably
about 5: 1 to about 15: 1, respectively, by weight.
The temperature and pressure of the contacting step is regulated so
that no boiling of water occurs in the combined biosludge/oil stream prior to
entry into the biosludge evaporator. It is important that no boiling occur at
this point because once boiling commences, the volume expansion is rapid
and of great magnitude. For example, one pound of steam has
approximately 1,000 times the volume of one pound of water. Thus velocity
and pressure drop increase radically unless ample space is provided in the
evaporator to separate the vapor from the rest of the biosludge/oil mixture.
Cell rupture is enhanced by rapidity of the pressure drop.
The hot oil and biosludge enter the evaporator through a pressure
reducing device. In the evaporator, water vapor is released from the
intracellular water content of the biosludge. The pressure reducing device is typically a valve located on the exterior inlet to the evaporator. As a result
of the contacting of the hot oil with the biosludge and the rapid pressure
reduction, the cell structure housing the intracellular water is weakened. The
weakened cell walls housing the intracellular water are then ruptured in the
evaporator, releasing the intracellular water. Some or all of the intracellular
water then vaporizes since the temperature of the biosludge/oil mixture
entering the evaporator is above the water saturation temperature at the flash
evaporator pressure.
Suitable pressures in the evaporator vary from about 0 to about 60
psia, and preferably about 0.5 to about 20 psia. Suitable temperatures of the
biosludge/oil mixture prior to the pressure reduction step are about 80°C to
about 350°C, and preferably about 90°C to about 250°C. As the water
evaporates, the overall temperature will drop. This is referred to by those
skilled in the art as an "adiabatic flash evaporation." The temperature in the
evaporator and fraction of water evaporated will be such that enthalpy of the
entering stream will equal the enthalpy of the streams leaving the evaporator
except for minor enthalpy or heat losses from walls of the vessel.
Water vapor exits the top of evaporator. The hot oil and concentrated
biosludge mixture exit the bottom of the evaporator. A portion of the
concentrated biosludge/oil mixture is passed to the gasifier. The remainder
is heated in a reboiler to provide the energy to convert the intracellular water released in the evaporation step to vapor. A separate stream of hot oil can be
used to heat the concentrated biosludge mixture which passes through the
reboiler. Additional oil can be added to the concentrated biosludge mixture
when needed, preferably at the heating oil inlet to the reboiler.
The hot oil and concentrated biosludge mixture that is heated in the
reboiler is then directly contacted with the biosludge feed material to form a
combined stream. The hot oil and concentrated biosludge mixture provide
sufficient heat to the combined stream to evaporate intracellular water from
the biosludge feed material in the evaporator.
The overhead vapor from the evaporator can be cooled by heat
exchange with the incoming biosludge or oil. The overhead vapor can then
be further cooled in a separate condenser or in a flash gas condenser. The
water condensed from the vapor can be used as a moderator in the partial
oxidation gasification reaction. Excess water can be routed to a wastewater
treatment plant to remove suspended and dissolved organic substances prior
to the discharge of the water in accordance with environmental regulations.
The reboiler can be heated with external steam or fuel or can use
some or all of the heat sources available from the partial oxidation
gasification system depending on the energy available. The partial oxidation
gasification system includes syngas trim coolers, syngas coolers, flashgas
condensers, or quench water coolers. The amount and sources of heat used will depend on the desired ratio of biosludge to oil and the water content of
the biosludge or sewage used.
Referring now to Fig. 1, biosludge stream 2 enters the heat exchanger
4 where it comes into indirect contact with hot water vapor stream 6 exiting
the top of the biosludge evaporator 8. The hot water vapor stream 6
indirectly preheats the biosludge 2 to a temperature of about 35°C to about
250°C. Cooled water vapor stream 10 which can also be a mixture of liquid
and vapor, exits heat exchanger 4 at a temperature of about 25°C to about
120°C, and enters the condenser 12 where it is divided into water stream 13,
which can serve as a moderator for the partial oxidation gasification reaction
(not shown), and water stream 14 which can be recycled to a waste water
treatment plant (not shown).
Heated biosludge stream 16 exits the heat exchanger 4 at a temperature
of about 30°C to about 240°C, and is contacted directly with the hot oil stream
18 exiting the reboiler 20 at a temperature of about 80°C to about 350°C to
form combined oil/sludge stream 22 at a temperature of about 105°C to
250°C. The hot oil stream 18 also contains a portion 30 of concentrated
biosludge from line 24 exiting from evaporator 8. The combined oil/sludge
stream 22 passes through the pressure reducing device 23 which is typically a
valve that causes the pressure of stream 22 to drop as it enters the biosludge
evaporator 8. The pressure is typically below the saturation pressure of water at the temperature of stream 22, for example, about 0.01 atmospheres
(.147 psia) to about 2 atmospheres (29.4 psia). The biosludge stream 16
contacts the hot oil stream 18 at a pressure which exceeds the water
saturation pressure at the temperature of stream 22. This prevents the
evaporation of water until stream 22 passes through the pressure reducing
device 23. The pressure can vary from about 0.1 atmospheres (1.47 psia) to
about 40 atmospheres (587.8 psia).
The hot oil stream 18 can be any oil with a heating value above about
8,000 BTU/pound. Typical examples of suitable oils include heavy crude
oil, fuel oil, atmospheric resid, vacuum resid, visbreaker tar, solvent
deasphalting residuum, or a combination of these oils.
The biosludge evaporator 8 operates at conditions which are designed
to rupture the bacterial cells containing the intracellular water of the
biosludge in stream 22. The chemical nature and temperature of the hot oil,
on the order of about 80°C to about 350°C, acts to weaken or disrupt the cell
walls of the biosludge housing the intracellular water.
The reduction of pressure from above the water saturation pressure at
the point of mixing of streams 18 and 16 to below the water saturation
pressure in the evaporator 8 causes a portion of the intracellular water to
vaporize, resulting in the rupturing of most of the bacterial cell walls of the
biosludge previously weakened due to the effect of the hot oil on the cell membranes. The intracellular water is released as vapor in stream 6 which
exits from the top of evaporator 8.
The hot oil and concentrated biosludge stream 24 which remains after
the release of the intracellular water exits the evaporator 8 at a temperature
of about 105°C to about 250°C.
The concentrated biosludge/oil stream 24 exiting the bottom of the
biosludge evaporator 8 is divided into oil/sludge streams 25 and 30.
Supplemental oil feed 26 from reservoir 40 can be combined as needed with
the oil/sludge stream 25 to form cogasification stream 28 which is
introduced into a partial oxidation gasification system (not shown) and used
as fuel for a partial oxidation reaction for the production of synthesis gas.
Ultimately, oil has to be added to the process to make up for losses of
oil in stream 25. This oil can be added in stream 42 upstream of the pump
32 or in stream 27 downstream of the pump 32, with the choice being
dictated by design preferences and the temperature and the pressure of
available oil.
The additional oil feed stream 42 from oil feed reservoir 40 can be
combined with oil/sludge stream 30 to form combined stream 44 which is
passed through the pump 32 and enters the reboiler 20. If the oil in reservoir
40 is available at sufficiently high pressure it can be added downstream of
pump 32 in stream 27 instead of upstream in stream 42. The ratio of the biosludge dry solids contained in stream 24 to the oil
in streams 27 and 42 varies from about 0.01 : 1 to about 1 : 1, and preferably
from about 0.1 : 1 to about 0.99: 1.
The reboiler 20 can be heated with steam, flashgas, or hot water, or
hot syngas introduced as stream 34 to provide the heat source for the reboiler
20, which exits as condensate, water, or cooled syngas stream 36.
The sources of heat used will depend on the ratio of biosludge to oil
desired and the water content of the biosludge used.
The ratio of oil/sludge stream 25 to concentrated oil/sludge feed 30
can range from about 1 :1 to about 1 :100, and preferably about 1 :2 to about
1 :50 respectively.
All parts and percentages indicated throughout the application are by
weight, unless otherwise indicated.
EXAMPLE
300 lbs of biosludge containing 4 weight % dry solids is treated in the
operating system of Fig. 1. After being preheated, the biosludge is combined
with 3100 lbs of a mixture comprising 2743.4 lbs oil, 329.2 lbs dry solids
and 27.4 lbs water. The heated combined biosludge/oil mixture then
undergoes pressure reduction and evaporation at 1.4 atmospheres (20.58
psia) which results in the rupture of the bacterial cell walls of the biosludge thereby releasing 287 lbs of intracellular water in the form of a hot aqueous
vapor and producing 3113 lbs of a concentrated biosludge/oil mixture which
exits the evaporator. The concentrated biosludge/oil mixture is divided into
a first stream of 113 lbs of biosludge/oil to provide a cogasification fuel
stream for a partial oxidation reaction.
The remaining 3000 lbs of the concentrated biosludge/oil mixture are
combined with 100 lbs of oil and pumped to the reboiler where the
combination is heated to 350°C and combined with incoming biosludge.

Claims

CLAIMSWhat is claimed is:
1. A method for concentrating a biosludge comprising a plurality
of bacterial cells with cell walls containing intracellular water, comprising:
(a) dewatering the biosludge to a dry solids content of at least
about 3 weight %;
(b) heating the dewatered biosludge at a temperature sufficient
to weaken the cell walls containing the intracellular water
and at a reduced pressure sufficient to rupture the
weakened cell walls and release the intracellular water; and
(c) evaporating the released intracellular water as a hot
aqueous vapor from the ruptured cells of the biosludge,
thereby producing a concentrated biosludge.
2. The method of claim 1, wherein the concentrated biosludge is
used as a fuel source for a partial oxidation gasification reaction.
3. The method of claim 1, wherein the dewatered biosludge is
heated by being directly contacted with a hot oil to form a hot oil/biosludge
mixture.
4. The method of claim 1, wherein the heating temperature used
to weaken the cell walls of the dewatered biosludge varies from about 80°C
to about 350°C.
5. The method of claim 1, wherein the rupture pressure varies
from about 0 psia to about 60 psia.
6. The method of claim 1 wherein the temperature for
evaporating the released intracellular water varies from about 105°C to about
250°C.
7. The method of claim 1, wherein the hot aqueous vapor is
condensed and used as a moderator in a partial oxidation gasification
reaction.
8. The method of claim 3, wherein the hot oil/biosludge mixture
is subjected to sufficient temperature and pressure to weaken, rupture, and
release the intracellular water from the biosludge, thereby producing a hot
concentrated biosludge/oil mixture.
9. The method of claim 3, wherein the dewatered biosludge is
preheated by indirect contact with the hot aqueous vapor released from the
ruptured cells of the biosludge before being contacted with the hot oil.
10. The method of claim 8, wherein the ratio of hot oil to
biosludge varies from about 1 : 1 to about 15: 1 respectively.
11. The method of claim 8, wherein the concentrated biosludge/oil
is combined with a sufficient amount of a hydrocarbonaceous material to
form a fuel for a partial oxidation gasification reaction.
12. The method of claim 11, wherein the ratio of concentrated
oil/biosludge to the hydrocarbonaceous fuel varies from about 1 :50 to about
1 : 1.
13. The method of claim 11, wherein the hydrocarbonaceous
material is an oil having a heating value of at least about 8,000 BTU/pound.
PCT/US1999/028617 1998-12-17 1999-12-03 Gasification of biosludge WO2000036056A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CA 2348787 CA2348787C (en) 1998-12-17 1999-12-03 Gasification of biosludge
JP2000588308A JP3849047B2 (en) 1998-12-17 1999-12-03 Biosludge gasification method
AU21634/00A AU745358B2 (en) 1998-12-17 1999-12-03 Gasification of biosludge
EP99965975A EP1141177B1 (en) 1998-12-17 1999-12-03 Gasification of biosludge
DE1999635251 DE69935251T2 (en) 1998-12-17 1999-12-03 GASIFICATION OF BIOSHYL
US09/807,267 US6436157B1 (en) 1998-12-17 1999-12-03 Gasification of biosludge

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US23168398A 1998-12-17 1998-12-17
US09/213,683 1998-12-17

Publications (1)

Publication Number Publication Date
WO2000036056A1 true WO2000036056A1 (en) 2000-06-22

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GB2458271A (en) * 2008-03-10 2009-09-16 Mch Systems Ltd Converting sewage to useful products

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JP2002192195A (en) * 2000-12-28 2002-07-10 Hitachi Kiden Kogyo Ltd Sludge solubilizing treatment apparatus
GB2458271A (en) * 2008-03-10 2009-09-16 Mch Systems Ltd Converting sewage to useful products

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