CA1062627A - Coalescence of oil in oil/water emulsions - Google Patents

Coalescence of oil in oil/water emulsions

Info

Publication number
CA1062627A
CA1062627A CA221,876A CA221876A CA1062627A CA 1062627 A CA1062627 A CA 1062627A CA 221876 A CA221876 A CA 221876A CA 1062627 A CA1062627 A CA 1062627A
Authority
CA
Canada
Prior art keywords
oil
fabric
fibrous structure
bonded
coalescer
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
CA221,876A
Other languages
French (fr)
Inventor
Barry Walker
David B. Chambers
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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
Priority claimed from GB10687/74A external-priority patent/GB1488682A/en
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Application granted granted Critical
Publication of CA1062627A publication Critical patent/CA1062627A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D17/00Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
    • B01D17/02Separation of non-miscible liquids
    • B01D17/04Breaking emulsions
    • B01D17/045Breaking emulsions with coalescers
    • 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
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/30Wastewater or sewage treatment systems using renewable energies
    • Y02W10/37Wastewater or sewage treatment systems using renewable energies using solar energy

Landscapes

  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Removal Of Floating Material (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Water Treatment By Sorption (AREA)
  • Manufacturing Of Multi-Layer Textile Fabrics (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Physical Water Treatments (AREA)
  • Colloid Chemistry (AREA)

Abstract

ABSTRACT OF THE DISCLOSURE
A method for removing oil from an oil in water emulsion which comprises passing the emulsion through a fibrous structure comprising fibres having finely divided particles which exhibit oleophilic and hydro-phobic properties penetrating their outer surfaces, and removing the coalesced oil droplets so formed.

Description

The present invention concerns the removal of oil from an oil in water emulsion According to the present invention we provide a method for the removal of oil from an oil in water emulsion which comprises passing the emulsion through a fibrous stxucture comprising fibres having finely divided particles which exhibit oleophilic and hydrophobic properties penetra~ing their outer surfaces, and removing the coalesced oil droplets 50 formed.
` The fibres, e,g, continuous filaments of staple fibres, may be homofibres to which the particles have been caused to adhere and penetrate their surfaces by subjecting the homofibres to surface heat and/or plasticiser treatment(s). Alternatively, the fibres may be homofibres with a non-fibre forming resinous or polymeric coating thereon,which coating when sub~ected to `~ heat and/or plasticiser treatment(s) and having particlen applied;thereto allows them to penetrate and adhere.
Most desirably, however, the fibres are conjugate fibres.
By the expression "conjugate fibre" is meant a spun, especially a melt spun, fibre (i.e. a continuous filament or a staple fibre) composed of at least two fibre-forming polymeric components arranged in distinct zones across the cross-section of the fibre and substantially continuous along the length thereof, and wherein one of the components has a melting temperature ~i significantly lower than the melting temperature (s) of the other components and is located so as to form at least a portion of the peripheral surface of the fibre.
Therefore, according to a preferred embodiment of the invention, the method utilizes a fibrous structure comprising ! oriented, conjugate fibres(as hereinbefore defined~, the component of lower melting temperature having finely divided particles which exhibit oleophilic and hydrophobic properties penetrating its outer surface.
-2 ,''' ~ .

~ - ~
~0626Z7 Conjugate fibres having two components are preferred.
The most preferred type of bicomponent fibre is one wherein a component of low melting temperature forms a sheath about another component serving as a core; although a bicomponent fibre wherein a component of low melting temperature is one o~ kwo components arranged side-by-side may also be used, - The polymeric material of the low melting point component has a melting point at least 10C, preferably at least 20C, below that of the other component of the fibre.
The fibrous structure may be in the form of a knitted fabric, a woven fabric or a non-woven fabric, the latter being preferred, Particularly desirable fibrous structures are melded -i fabrics produced from staple fibres or oriented, i.e. drawn, sheath/core heterofilaments. Such melded fabrics may either be point-bonded or area-bonded, Any one fibrous structure may comprise more than one layer of fabric.
,' The preferred particles are silane-coated silica i particles, although other particles which exhibit the combined properties of oleophilicity and hydrophobicity may be used, The average size of particle is preferably at least 0.1 micron, The "average size of particle" indicates the largest cross-sectional -~ dimension of a particle,e.g. the diameter in the case of a :' spherical particle. Most desirably the particles have an average , "
size of one micron or less, ,''.' .

:.lt - 3-.

'~1 ;
.~ :

.. . .
'', : ~.. , ,. ... ., . ., . , ... -.

~ he degree of hydrophobicity of the fibre~ should be such that the fibrous structure effects a water contact angle of at least 110 and preferably greater than 140. The magnitude of the contact angle is largely dependent on the type of hydro-phobic particles used and its concentration per unit area at the surface of each fibre. The oleophilic nature of the particles exposed on the fibres is such that the oil comes into contact with, and temporarily adheres to, the particles and the oil droplets then coalesce and pass through the fibrous structure.
The process is thought to be enhanced by the surface roughness of the fibres due to the presence of the particles, The porosity of the fibrous structure is chosen such that the probability of the oil particles contacting the fibres is as high as possible without creating too high a pressure drop ::
across the fibrous structure. Of the preferred fibrous structures, point-bonded melded fabrics, being more tightly packed, have a much higher pressure drop than area-bonded melded fabrics. With both point-bonded and area-bonded melded fabrics, the pressure drop is usually less than 50 cm of water at hydraulic flows up to 16m3 per hour per square metre of fabric, However the pressure drop will increase above this figure as the hydraulic flow and/or oil throughput is increased, By "point-bonded fabric" we mean a fabric in which the fibres have small discrete regions in which the fibres are strongly adhesively bonded to each other, which regions are separ-ated from each othex by less strongly bonded, or even unbonded, regions.
. .
'.' .i~ .
.

. .. . . ~ :
: , 106;~627 By "area-bonded melded fabric" we mean a fabric the fibres in which are adhesively bonded to each other at substantially all cross-over points throughout the thickness and over the whole area of the material.
Particularly efficient fibrous structures are those comprising two or more superimposed area-bonded melded fabrics followed by one or more point-bonded melded fabrics. With a fibrous structure comprising three superimposed area-bonded meldea fabrics followed by a superimposed point-bonded melded fabric it is possible to achieve in excess of 97% and some~imes ` in excess of 9~/O reduction in oil concentration, after allowing sufficient time, for example 4 to 8 minutes for gravimetric separation of the coalesced oil droplets, by a singla pass through the fibrous structure at hydraulic flows up to 9 2m3 per hour per square metre of fabric.
With other fibrous structures such as two superimposed area-bonded melded fabrics followed by a superimposed point-bonded melded fabric or two superimposed area-bonded fabrics, the efficiency is not as high. Nevertheless, as the pressure drop through such fibrous structures will ~e lower, they may be preferable when high loadings are required.
In order that the fibrous structures described herein .; .
can operate with maximum efficiency it is desirable that the fl~w of oil in water emulsion through the structure is substantially , uniform across the structure. Conveniently this can be achieved I by passing the emulsion through a suitably shaped and dimensioned sheet or block of an open-cell expanded plastics material located immediately upstream of the fibrous structure.
Apart from serving to distribute the flow substantially across the fibrous structure~ the presence of the cellular plastics material on the upstream side of the fibrous structure . , .

, ' :
.

,. .
:

10f~26;~7 serves to prevent extraneous matter e g solid particles and large oil droplets from entering, and causing blockage in ~he fibrous structure.
A particularly desirable expanded plastics material for this purpose i5 a hydrophilic plastics material such as a hydro-philic polyurethane foam.
The fibrous structures used in the invention may have any suitable shape. Though the fibrous structure may be in the for~ of a sheet or block having substantially planar faces, the-fibrous structure may have a tubular form. In the latter case the oil in water emulsion can either be passed from inside to outside or from outside to inside of the fibrous structure.
In practice, however, when the fibrous structure is in the form of a tube, we find it more convenient to pass the oil in water emulsion into the inside of the tube and allow it to flow through the wall of the tube. We have found that by adopting this expedient, the oil/water mixture after passing through the fibrous structure tends to adopt a linear flow and ` this encourages the coalesced oil droplets to separate from the water by gravity, The method of the present invention can be used with either vegetable or mineral oil emulsions. The method has been ; founded to be particularly effective for achieving caalescence of a variety of both vegetable and mineral oil emulsions for example emulsions from the cleaning of tankers or storage vessels used to transport mineral and vegetable oils, ballast water in crude oil tankers and oil containing coolants.
The invention will now be described with reference to the following Examples.

~ ~ .

, .

.

A point-bonded, melded fabric of 137 gm, per square metre, produced from staple fibres of oriented, i.e. drawn, sheath/core heterofilaments in which the core(5~/0 by weight of total weight of filament) was polyethylene terephthalate of melting point 257C and the sheath was a copolymer of poly-ethylene terephthalate and polyethylene adipate (85:15 mole ratio) o~ melting point 220~C, was passed through a 2%
dispersion of silane~coated sîlica particles ~"Silanox 101", Trade ~ark; manufactured by Cabot Corporation; primary particle size 7 milli-midrons; BET surface area 225 m2/gm) in trichloro~
ethylene. The dried fabric was held at constant area on a pin stenter frame whilst being heated at 217C for ten minutes, and finally rinsed with water to remove loosely adhering particles.
Dropstof water placed on the dried fabric had a mean contact angle of 15S, This fabric was designated Fabric A, ., An area-bonded, melded fabric of smiliar construction , was treated in a similar manner, This fabric was designated Fabric B.

~ A coalescer was produced by forming a four component `~ lay-up by superimposing one piece of Fabric A and three pieces . .~ .
of Fabric B in that order. The fibrous structure so formed was ~`, sufficiently strong to allow it to be fixed in position as a common wall between two reservoirs X and Y, the area-bonded -~ face of the structure i.e. Fabric B facing reservoir X and the i point-bonded face of the structure i.e, Fabric A facing reservoir Y.
Each reservoir was fitted with a floating arm take-off which could be adjusted so that any oil floating to the surface of the oil/water emulsion in the reservoir could be skimmed off.

lO~Z627 Water from the mains was fed by a rotometer into reservoir X. Oil was fed from a barrel directly into the stream of water entering the reservoir and an oil in water emulsion was produced containing 236 ppm of oil, When the reservoir X had filled up, the flow into the reservoir X was adjusted to retain a constant depth of oil/water The emulsion flowed through the coalescer into reservoir Y until eventually a constant depth of liquid was produced. At this stage, in order to keep a steady state, liquid was drained out of reservoir Y at the same rate as it entered reservoir X. The variation in pressure head across the coalescer was 10.5 cm of water at a constant flow of 9.2m3 per hour per square metre of fabric.
Initial coalescence of oil droplets on the down-stream side of the coalescer was very slow and consisted of very small oil droplets. However, after 3 or 4 hours, coalescence was much faster and the size of the oil droplets formed were much larger and floated towards, and formed a layer on, the , free surface of the liquid in reservoir Y.
At this stage, samples of the oil/water emulsion were taken at about 30 minute intervals at a location O within .:
` reservoir X immediately on the upstream side of the coalescer and also at a location P within reservoir Y remote from the downstream side of the coalescer after separation of the oil by gravity had occured. With a hydraulic flow of 9.2m3 per hour per square metre of fabric the liquid leaving the coalescer was allowed to settle for 6 minutes before it arrived ~ at location P.
., .
i! -B-. ~
I!

106Z6'~7 With this hydraulic flow an average oil concentration of 236 ppm ~at location Oj was reduced to an average of 0,9 ppm (at location P)continuously over a 7 hour periodO
The efficiency of the coalescer was then studied with various flow rates with equally good results.
EX~MPLE 2 Example 1 was repeated in entirety (apart from oil concentration and flow rate) except that the coalescer was ! '~ produced by forming a three component lay-up by superLmposing two pieces of Fabric B and one piece of Fabric A.
The following results were obtained:-The pressure drop across the coalescer was 26 mm of ` water, The oil concentration was reduced from 690 ppm(at location 0) to 17 ppm (at location P) over a four hour period at a hydraulic flow of 9.8m3 per hour per square metre ' of fabric.

~, Example 1 was repeated in entirety (apart from oil ' 20 concentration and flow rate) except that the coalescer was 1! produced by forming a two component lay-up by superimposing ... ':! ' .
two pieces of Fabric B.

The following results were obtained:-The pressure drop across the coalescer was 3 cm of water.

The oil concentration was reduced from 684 ppm ~ . .
(at location 0) to 43 ppm (at lo~ation P) over a four hourperiod at a hydraulic flow of 8m3 per hour per square metre of fabric.

g_ .~ :

: ':

;, ...
,", .

Example 1 was repeated in entirety (apart frcm oil concentration and flow rate) except that the coalescer was a single piece of Fabric A, The following results were obtained:-The pressure drop across the coalescer was 10 cm ofwater~ The oil concentration was reduced from 289 ppm (at location O) to 36 ppm (at location P) over a four hour period at a hydraulic flow of lO.Sm3 per hour per square metre of fabric.
This shows that particularly efficient coalescers are fibrous structures comprisin~ two or more superimposed area-bonded fabrics followed by one or more point-bonded melded fabrics as described herein.
;~ EXAMPLE 5 As a comparison, Example 1 was repeated except that r~ the coalescer was produced by forming a four component lay-up by superimposing three pieces of Fabric Atbefore it had been treated with silane-coated silica particles as described in Ex~mple 1) and one piece of Fabric B(before it had been treated with silane-coated silica particles as described in Example 1).
,,. .~
The pressure drop across the coalescer was now 14.5 cm , of water. The oil concentration was reduced from 232 ppm (at location 0) to 38 ppm over a four hour period(at location P) at a hydraulic flow of 11.6m3per hour per square metre of fabric.
This shows that the coalescer used in Example 1 has a much higher efficiency than the coalescer used in ~he present Example.

:! -- 10 --:

A coalescer was produced by superimposing two pieces of Fabric B, This was fixed in position as a common wall between reservoirs X and Y.
Effluent from the cleaning of road tankers used in : the transport of mineral oils and vegetab~ oils with steam and paraffin based detergents was passed into reservoir X, Liquid was drained out of reservoir Y at the same rate as it entered reservoir X, The variation in pressure head across the coalescer wa.q a maximum of 20 centimetres of water at a constant flow of 16 cubic metres per hour per square metre of fabric.
: Samples of the 'oil'/water emulsion were taken at regular intervals at a location O within reservoir X immediately on the upstream side of the coalescer and also at a location P
~, within reservoir Y remote from the downstream side of the coalescer after separation of the 'oil' by gravity had occurred.
The results of separation achieved are given .20 in the table below .

: "Oily"Oil Content ppm Oil Content ppm .
: Componentof Effluent after coalescence ;.' at location O at location P .
_ _ .
. Palm Oil 153 88 '. Sunflower Oil/ 36 23 :
.. ~ Spindle/Crude Rape Oil .~. Plasticiser 212 115 :

.~ Lead Naphthalate/
~ Mineral Oil 592 290 : 30 Chrome Liquor/
Mineral Oil 260 168 -- After extended use,the coalescer was successfully -, cleaned with a jet of steam/hot water and after cleaning was . re-used. -11-" ' - -: . - : ' ,: ~ . : . . '

Claims (2)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:-
1. A method for the removal of oil from an oil in water emulsion by passing the emulsion through a fibrous structure and removing the coalesced oil droplets so formed the improve-ment comprising a fibrous structure comprising fibres having finely divided particles which exhibit oleophilic and hydrophobic properties penetrating their outer surfaces.
2. A method for the removal of oil from an oil in water emulsion comprising passing the emulsion through an open-cell expanded plastics material and then through a fibrous structure comprising fibres having finely divided particles which exhibit oleophilic and hydrophobic properties penetrating their outer surfaces and removing the coalesced oil droplets so formed.
CA221,876A 1974-03-11 1975-03-11 Coalescence of oil in oil/water emulsions Expired CA1062627A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB10687/74A GB1488682A (en) 1974-03-11 1974-03-11 Coalescence of oil in oil/water emulsions
GB4407874 1974-10-11

Publications (1)

Publication Number Publication Date
CA1062627A true CA1062627A (en) 1979-09-18

Family

ID=26247693

Family Applications (1)

Application Number Title Priority Date Filing Date
CA221,876A Expired CA1062627A (en) 1974-03-11 1975-03-11 Coalescence of oil in oil/water emulsions

Country Status (13)

Country Link
JP (1) JPS5439066B2 (en)
BR (1) BR7501406A (en)
CA (1) CA1062627A (en)
CH (1) CH592463A5 (en)
DE (1) DE2509649C3 (en)
DK (1) DK98675A (en)
ES (1) ES435493A1 (en)
FR (1) FR2263803A1 (en)
IT (1) IT1034185B (en)
LU (1) LU72025A1 (en)
NL (1) NL7502731A (en)
NO (1) NO138126C (en)
SE (1) SE7502651L (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2326965A1 (en) * 1976-10-11 1977-05-06 Infraroedteknik Ab Filter to remove hydrocarbons from used aerosols - comprises mineral particles treated with lipophilic substances
JPS5942906U (en) * 1982-09-14 1984-03-21 株式会社第一測範製作所 Alignment inner diameter measuring device
GB2135207B (en) * 1983-02-17 1986-02-05 Shell Int Research Process and apparatus for the removal of oil from an oil-in-water dispersion
GB8513794D0 (en) * 1985-05-31 1985-07-03 Keene Int Ltd Fuel filter
DE3703239A1 (en) * 1987-02-04 1988-08-18 Ideal Standard MIXED BATTERY
GB8711931D0 (en) * 1987-05-20 1987-06-24 British Petroleum Co Plc Filtration/coalescence

Also Published As

Publication number Publication date
DK98675A (en) 1975-09-12
CH592463A5 (en) 1977-10-31
NO138126B (en) 1978-04-03
LU72025A1 (en) 1976-08-19
SE7502651L (en) 1975-09-12
IT1034185B (en) 1979-09-10
ES435493A1 (en) 1977-03-16
FR2263803A1 (en) 1975-10-10
DE2509649B2 (en) 1979-09-13
NO138126C (en) 1978-07-12
DE2509649A1 (en) 1975-10-30
DE2509649C3 (en) 1980-05-29
BR7501406A (en) 1975-12-09
JPS514861A (en) 1976-01-16
JPS5439066B2 (en) 1979-11-26
NL7502731A (en) 1975-09-15
NO750728L (en) 1975-09-12

Similar Documents

Publication Publication Date Title
US4199447A (en) Coalescence of oil in oil/water emulsions
US3960719A (en) Coalescence filter for oil-water dispersions
US3764527A (en) Method for separating oil from water
US3450632A (en) Method for simultaneously coalescing,filtering and removing oil traces from liquids and media for accomplishing the same
Dong et al. Highly efficient and recyclable depth filtrating system using structured kapok filters for oil removal and recovery from wastewater
US4663222A (en) Non-woven fabric, and oil water separating filter and oil-water separating method
US4070287A (en) Polymeric and cellulosic fiber material for removing oil from water
CA2114303C (en) Method of making sorbent articles
EP0208515A2 (en) Filter process and filters therefor
US5252215A (en) Adsorbent materials and use thereof
US3738492A (en) Oil-water separator
EP0030569A1 (en) Apparatus for the separation of oil from dispersions
US4102783A (en) Adsorbent process for oily materials
CN105477903A (en) Surface coalescer
US4168229A (en) Removal of oil from an oil in water emulsion
NO162545B (en) FILTERS FOR SEPARATION OF SUBSTANCES WITH LIPOFILE AND / OR OLEOFILE AND / OR UNPOLAR PROPERTIES FROM OTHER LIQUIDS, GASES AND STEAMS.
CA1062627A (en) Coalescence of oil in oil/water emulsions
US5156767A (en) Emulsion breaking using alkylphenol-polyethylene oxide-acrylate polymer coated coalescer material
Zahid et al. Oil slick removal using matrices of polypropylene filaments
GB2273669A (en) Liquid/liquid separation
US6395184B1 (en) Method for dehydrating crude oil and petroleum products and device for realizing the same
DE2634185A1 (en) METHOD OF REMOVING OIL FROM AN OIL-IN-WATER EMULSION
Ge et al. Electrospun nanofibers for oil–water separation
CA1178542A (en) Method and apparatus for oil-water separation by coalescence
CA1114749A (en) Apparatus for the treatment of liquids and method for cleaning a layer of fibres in such an apparatus