WO2006041372A1 - Method and system for on-line monitoring - Google Patents

Method and system for on-line monitoring Download PDF

Info

Publication number
WO2006041372A1
WO2006041372A1 PCT/SE2005/001338 SE2005001338W WO2006041372A1 WO 2006041372 A1 WO2006041372 A1 WO 2006041372A1 SE 2005001338 W SE2005001338 W SE 2005001338W WO 2006041372 A1 WO2006041372 A1 WO 2006041372A1
Authority
WO
WIPO (PCT)
Prior art keywords
loop
sample
reactor
tempering
sub
Prior art date
Application number
PCT/SE2005/001338
Other languages
English (en)
French (fr)
Inventor
Johnny Lundberg
Original Assignee
Akzo Nobel Coatings International Bv
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 Akzo Nobel Coatings International Bv filed Critical Akzo Nobel Coatings International Bv
Priority to UAA200705206A priority Critical patent/UA83596C2/ru
Priority to EP05784657A priority patent/EP1802391A1/en
Priority to BRPI0517544-5A priority patent/BRPI0517544A/pt
Priority to CA002581850A priority patent/CA2581850A1/en
Publication of WO2006041372A1 publication Critical patent/WO2006041372A1/en
Priority to NO20072403A priority patent/NO20072403L/no

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0006Controlling or regulating processes
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00Sampling; Preparing specimens for investigation
    • G01N1/02Devices for withdrawing samples
    • G01N1/10Devices for withdrawing samples in the liquid or fluent state
    • G01N1/20Devices for withdrawing samples in the liquid or fluent state for flowing or falling materials
    • G01N1/2035Devices for withdrawing samples in the liquid or fluent state for flowing or falling materials by deviating part of a fluid stream, e.g. by drawing-off or tapping
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00002Chemical plants
    • B01J2219/00004Scale aspects
    • B01J2219/00006Large-scale industrial plants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00168Controlling or regulating processes controlling the viscosity
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00177Controlling or regulating processes controlling the pH
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00Sampling; Preparing specimens for investigation
    • G01N1/02Devices for withdrawing samples
    • G01N1/10Devices for withdrawing samples in the liquid or fluent state
    • G01N1/20Devices for withdrawing samples in the liquid or fluent state for flowing or falling materials
    • G01N1/2035Devices for withdrawing samples in the liquid or fluent state for flowing or falling materials by deviating part of a fluid stream, e.g. by drawing-off or tapping
    • G01N2001/2064Devices for withdrawing samples in the liquid or fluent state for flowing or falling materials by deviating part of a fluid stream, e.g. by drawing-off or tapping using a by-pass loop

Definitions

  • the present invention relates in general to a method for measuring a plurality of parameters in chemical processes where tempered measurements on liquid media is a requirement and a system therefore.
  • the system is particularly suitable for use in resin ) manufacturing.
  • monitoring of process parameters of chemical production processes by means of automated operating systems is well-known in the art. Some monitoring systems require human intervention, including manual sampling of the liquid medium for further processing in separate measurements or analysis equipment, possibly in a laboratory remote from the sampling site. These systems are labour-intensive, and the results from them are often not swiftly obtained.
  • the measurements are carried out at about the same temperature that prevails inside the reactor.
  • the temperature of the medium in these systems is not adjusted.
  • the measurement temperature may play a considerable role to obtain accurate results. This is the case when measuring e.g. the viscosity, pH and many other process parameters.
  • the viscosity of the reaction medium of a solution of two reactants in a reaction vessel may be very similar at an elevated reaction temperature but fairly different at a lower temperature. The measurement at a lower temperature may then provide more accurate results.
  • Non-tempered technology is disclosed in US 6,635,224 illustrating an on-line polymer monitoring apparatus for rapid determination of various polymer properties.
  • in-line system refers to a system where a sample flow of a process medium, the parameters of which is to be determined, is passed through a side-loop in which measurement equipment is arranged.
  • the temperature of the sample flow will be essentially the same as in the reactor, and is thus not adjusted.
  • on-line system refers to a system in which a sample flow of a process medium is withdrawn from the reactor and passed into a closed loop, separated from the reactor, wherein means for tempering the medium is provided, thus enabling measurements to be made at an adjusted and controlled temperature, that differs from the reactor temperature. It has been found that this type of closed loop provides for much more accurate measurements compared to open continuous loops which continuously circulates flow back to the reactor.
  • process medium is meant to encompass all reactants taking part or other components or substances present in the reactor where the chemical process is performed such as solvents, solutions etc.
  • sample as used herein, is meant a part or fraction of the process medium withdrawn from the reactor used for measurements of process parameters.
  • Fig. 1 is a schematic illustration of an automated, tempered combined in-line/on ⁇ line system according to one embodiment of the present invention
  • Fig. 2 shows viscosity vs. temperature curves for two resins
  • Fig. 3a is a side view of a sieve for use in the system according to the invention
  • Fig. 3b is a view from the outlet end of the sieve.
  • Fig. 1 shows a system comprising a batch reactor (reactor vessel) 2 in which a manufacturing process of resin is carried out.
  • Agitating means 4 driven by a suitable motor is provided in the reactor vessel.
  • an outlet 18 is located at the bottom of reactor vessel 2, to which a pipe segment
  • a valve V1 is mounted in pipe segment 20.
  • Pipe segment 20 is diverted in two pathways by pipe segments 22 and 24 respectively.
  • a valve V3 is mounted, and a first loop formed by pipe segments 20 and 22 is completed by a further pipe segment 26, connected to inlet 28 at the bottom of reactor vessel 2, which inlet is preferably not too close to outlet 18.
  • a valve V2 is mounted in pipe segment 26 in pipe segment 26, a valve V2 is mounted.
  • a means for circulating the sample, preferably a pump 30, for passing sample medium through the system is provided in pipe segment 24.
  • Segment 24 is diverted in two pathways by pipe segments 32 and 34.
  • a valve V6 is provided in segment 32 .
  • Segment 32, 22, 24, and 36 complete a second loop.
  • a measurement box 38 is provided further described below.
  • the side-loop formed by pipe segments 20, 24, 32, 36 and 26 forms an "in-line measurement loop".
  • a third loop is formed by pipe segments 20, 24, 34, 40, 42, 36, and 26.
  • a valve V4 and a sieve 44 are provided, the function and design of which will be further illustrated below.
  • a heat exchanger 46 for tempering a passing sample to a desired temperature.
  • a valve V5 is provided in the segment 42.
  • the isolated or separated side-loop formed by pipe segments 22, 24, 34, 40, 42 and 36 will be referred to as an "on-line measurement loop".
  • Cooling medium may be passed through heat exchanger 46 via a suitable valve V7 from inlet pipe 50 to outlet pipe 52.
  • V7 a suitable valve
  • the first loop made up of pipe segments 20, 22, and 26 has no function per se.
  • the entire loop system has a capacity of about 40 litres of sample, and is contemplated to be used with a reactor having a volume of 50 m 3 .
  • the sample constitutes about 0.08 % of the total reactor volume.
  • suitable sensors for pH and viscosity measurements respectively are TBI-Bailey (pH) and
  • BTG-KaIIe viscosity
  • Other suitable sensors may include e.g. a commercial turbidity sensor such as a Dual Beam Scattered-Light Sensor from Optek-Danulat, GmbH - Essen, Germany as well as NlR spectroscopy equipment for collecting spectrometrical .data from process media, e.g. an lnteractance Immersion System 6500 from FOSS.
  • a plate heat exchanger is suitably used to temper the process media.
  • Measurement box 38 suitably comprises an elongated tube, in which the sensor/sensors preferably are mounted to measure the temperature of the sample and preferably also to monitor the cooling capacity of the heat exchanger regulating the temperature of the sample.
  • Variation in cooling capacity can thus be monitored and cleaning of the cooler may be made accordingly.
  • two sensors are mounted in either end of the box.
  • a volume change will occur, leading to pressure changes.
  • Such pressure/volume changes are preferably adjusted by keeping valve V1 open during the tempering phase.
  • the compensators are essentially comprised of rubber elements having the necessary flexibility. These compensators act to reduce vibrations in the measurement box, which is beneficial for the viscosity measurement in particular.
  • the means for circulating the sample preferably a pump, may be shut off when the tempering phase has been completed and the measurement of the process parameters is to begin. This is advantageous in the sense that the process parameters, e.g.
  • the viscosity, the pH, conductivity, turbidity or spectrometrical data can be measured while the sample is standing still in the pipe segments.
  • the sample flow may otherwise, if flowing through the measuring equipment, disturb the measurements and render them less accurate. This may be due to particles dissolved in the sample flow.
  • the flow also may cause turbulance, physical forces on the sensor. Further contaminants besides particles, e.g. bubbles, wood chips in certain production lines, can be wholly or partially eliminated. Particles and the like can also be eliminated by means of filter means as further disclosed herein.
  • step 1 a pH adjustment is carried out in the beginning of the process (step 1).
  • a pH determination is made again during step 2 and initially in step 3 after which the viscosity is measured.
  • measurements should be made at 25 0 C, the process temperature in the reactor vessel during the condensation reaction being 9O 0 C.
  • step 4 again pH is determined.
  • in-line mode For the pH measurements (steps 1 , 2 and 4), "in-line mode" is used. Thereby, the in-line measurement loop defined by pipe segments 20, 24, 32, 36 and 26 is established by opening valves V1 , V2, V6, and closing valves V4, V5, and V3. Pump 30 pumps process medium from reactor 2 through the in-line loop and the medium will thus pass through measurement box 38 where a pH meter is located. The medium is pumped through box 38 for a time sufficient for allowing the pH reading to stabilise. Then the reading is taken as an indication of the pH prevailing in the reactor. .
  • the pH meter (not shown as such) is thus located inside measurement box 38.
  • glass material comprised in the measurement head of the pH meter is affected by the process conditions, especially the composition of the process medium, and compensations for variations may be made by means of controlling software.
  • the "on-line mode" is used for the viscosity measurement (step 3).
  • the on-line measurement loop defined by pipe segments 22, 24, 34, 40, 42, and 36 is established by closing valves V1 , V2 and V6, and opening valves V3, V4 and V5.
  • the process medium sample is pumped from the reactor into the above defined loop to fill it with the medium to be considered, and when the "on-line loop" defined above is filled, valves V1 and V2 are closed.
  • the medium is circulated through the heat exchanger 46.
  • the heat exchanger is fed with a suitable cooling medium through inlet 50, until the temperature has reached a desired level.
  • the flow of cooling medium may be switched off with valve V7.
  • a temperature sensor (not shown) is also located inside measurement box 38. Of course, the pH may be continuously monitored during tempering if desired.
  • tempering is especially important for viscosity measurements but also when measuring other temperature sensitive parameters.
  • the viscosity differs very little between different substances, which fact is evident from Fig. 2 showing viscosity vs. temperature for two different resins.
  • the difference is almost negligible at IOO°C, whereas at room temperature (approximately 20 0 C) 1 the difference is substantial.
  • measurements at higher temperatures require extreme accuracy in the equipment to be used.
  • Even if the equipment is accurate, the measurement is affected by various phenomena, e.g. vibrations, small solid particles present in the flow etc. These relatively small disturbances may still have a very large influence on the measurements. It has been found that only 1-5 minutes may be required before a reliable measurement can be performed on a tempered sample which enables accurate monitoring. In the process example above, only in-line measurement and on-line tempering/measurement modes were discussed.
  • valve V3 is closed and valves V1 and V2 are opened, thereby emptying the loop through reactor vessel inlet 28 and pumping fresh sample into the loop through reactor vessel outlet 18.
  • This exchange phase is terminated when the temperature at the inlet 28 equals the temperature at the outlet 18.
  • the heat exchanger is preferably inoperative, i.e. valve V7 is switched off to prevent cooling medium to pass through the heat exchanger. At this time, i.e. when the inlet and outlet temperatures equal each other, the system is ready for another on-line mode operation
  • non-tempering function when using a sensor with a relatively slow equilibrating time (e.g. pH meter), it may be desirable to isolate a sample flow without tempering it in the heat exchanger. This may be done by closing valves V1 , V2, V4 and V5, and opening valves V3 and V6. Thus, the sample is circulated through the measurement box 38 for a time sufficient for the sensor in question to reach an equilibrium state. This function will be referred to as a "non-tempering function".
  • Such cleaning does not form part of the invention per se, and should in fact be tailored for each individual process set up, like an ordinary washing machine setting. Since the various loops for the different measurement modes form sub-loops of the entire side-loop system, and since they are inter-connected by means of a number of valves, it is possible to perform practically instantaneous switching between the various modes, simpiy by opening and closing appropriate valves. As a consequence, the control of a chemical process where a number of different parameters need to be monitored within short time frames is greatly simplified and made much more efficient.
  • the process medium is contaminated by small particles, fibres and other debris that has managed to pass the pump without having been comminuted to a sufficiently small size.
  • the distance between the plates in the heat exchanger is critical
  • the distance is commonly about 4 mm, but may of course vary among different manufacturers.
  • a sieve may be provided upstream the heat exchanger. This sieve is not necessary for the function of the system according to the invention, but is primarily provided as a security precaution. However, measurements of e.g. viscosity could be adversely affected by the presence of the mentioned objects in the flow, and thus the sieve may nevertheless be beneficial for the successful operation of the invention.
  • the sieve shown in Figs. 3a and 3b, and generally designated 44 comprises an elongated box 54 made of acid proof steel, and has a generally rectangular cross section.
  • the mesh structure 62 comprises a mesh 66, mounted in a thin acid proof frame structure (not shown in the figure).
  • ridges 70 and 72 on each vertical wall 74 and 76 in box 54.
  • the ridges extend from the bottom of the box at the outlet end diagonally upwards to the upper part at the inlet end of the box, and thus, these pairs of ridges form a respective guide means in which the assembly of mesh and frame is inserted through an opening 78

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Health & Medical Sciences (AREA)
  • Pathology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)
  • Investigating Or Analyzing Materials Using Thermal Means (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
PCT/SE2005/001338 2004-10-12 2005-09-15 Method and system for on-line monitoring WO2006041372A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
UAA200705206A UA83596C2 (ru) 2004-10-12 2005-09-15 Способ и система осуществления мониторинга в режиме он-лайн
EP05784657A EP1802391A1 (en) 2004-10-12 2005-09-15 Method and system for on-line monitoring
BRPI0517544-5A BRPI0517544A (pt) 2004-10-12 2005-09-15 método e sistema para monitoramento online
CA002581850A CA2581850A1 (en) 2004-10-12 2005-09-15 Method and system for on-line monitoring
NO20072403A NO20072403L (no) 2004-10-12 2007-05-11 Fremgangsmate og system for online ovevaking

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04445109.4 2004-10-12
EP04445109 2004-10-12

Publications (1)

Publication Number Publication Date
WO2006041372A1 true WO2006041372A1 (en) 2006-04-20

Family

ID=34933002

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE2005/001338 WO2006041372A1 (en) 2004-10-12 2005-09-15 Method and system for on-line monitoring

Country Status (12)

Country Link
EP (1) EP1802391A1 (ru)
CN (1) CN101039746A (ru)
AR (1) AR054687A1 (ru)
BR (1) BRPI0517544A (ru)
CA (1) CA2581850A1 (ru)
MY (1) MY138506A (ru)
NO (1) NO20072403L (ru)
PE (1) PE20060808A1 (ru)
RU (1) RU2372981C2 (ru)
UA (1) UA83596C2 (ru)
WO (1) WO2006041372A1 (ru)
ZA (1) ZA200702923B (ru)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008080363A1 (en) * 2006-12-29 2008-07-10 Accelergy Shanghai R & D Center Co., Ltd. High throughput propylene from methanol catalytic process development method
WO2008080362A1 (en) * 2006-12-29 2008-07-10 Accelergy Shanghai R & D Center Co., Ltd. High throughput clean feed hydroprocessing development method

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2700331C1 (ru) * 2018-10-19 2019-09-16 Дарья Сергеевна Нехорошева Ик-спектрометрическая система парофазного контроля химического состава смесей жидких углеводородов в резервуаре и способ выполнения спектрометрических измерений с ее использованием

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3944824A (en) * 1973-09-21 1976-03-16 Entreprise De Recherches Et D'activites Petrolieres Elf Method and device for sampling gases
GB2170909A (en) * 1985-02-08 1986-08-13 Spectra Tek Uk Limited Apparatus and method for monitoring crude oil
US4735779A (en) * 1984-01-17 1988-04-05 Haendel Max D Method for testing the viscosity of synthetic resins and apparatus for the implementation of the method
US5944991A (en) * 1997-11-21 1999-08-31 Dresser Industries, Inc. Pipeline strainer
US6635224B1 (en) * 1998-10-30 2003-10-21 General Electric Company Online monitor for polymer processes

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3944824A (en) * 1973-09-21 1976-03-16 Entreprise De Recherches Et D'activites Petrolieres Elf Method and device for sampling gases
US4735779A (en) * 1984-01-17 1988-04-05 Haendel Max D Method for testing the viscosity of synthetic resins and apparatus for the implementation of the method
GB2170909A (en) * 1985-02-08 1986-08-13 Spectra Tek Uk Limited Apparatus and method for monitoring crude oil
US5944991A (en) * 1997-11-21 1999-08-31 Dresser Industries, Inc. Pipeline strainer
US6635224B1 (en) * 1998-10-30 2003-10-21 General Electric Company Online monitor for polymer processes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008080363A1 (en) * 2006-12-29 2008-07-10 Accelergy Shanghai R & D Center Co., Ltd. High throughput propylene from methanol catalytic process development method
WO2008080362A1 (en) * 2006-12-29 2008-07-10 Accelergy Shanghai R & D Center Co., Ltd. High throughput clean feed hydroprocessing development method

Also Published As

Publication number Publication date
RU2372981C2 (ru) 2009-11-20
EP1802391A1 (en) 2007-07-04
CA2581850A1 (en) 2006-04-20
AR054687A1 (es) 2007-07-11
PE20060808A1 (es) 2006-10-23
CN101039746A (zh) 2007-09-19
NO20072403L (no) 2007-05-11
MY138506A (en) 2009-06-30
BRPI0517544A (pt) 2008-10-14
RU2007117709A (ru) 2008-11-20
ZA200702923B (en) 2008-09-25
UA83596C2 (ru) 2008-07-25

Similar Documents

Publication Publication Date Title
US6297505B1 (en) Method and flow system for spectrometry and a cuvette for the flow system
CN106525905B (zh) 具有电极自动清洗和标定的水质在线监测系统
WO2006041372A1 (en) Method and system for on-line monitoring
WO2015198730A1 (ja) 自動分析装置
BR112017006530B1 (pt) analisador de líquidos
US20060078843A1 (en) System
JP4594764B2 (ja) 水質計測用の前処理装置
JP2008235812A (ja) 基板処理装置の供給異常検知方法及びそれを用いた基板処理装置
JP5003614B2 (ja) 生体細胞の分離方法及び培養装置
CN108020444B (zh) 一种水位随动采样系统
JP2000121628A (ja) 水質測定装置
CN109676114A (zh) 一种铝棒铸造用循环水恒温控制系统及方法
US4297213A (en) Apparatus for separating and contacting friable particulate organic matter from and with liquids
CN210496364U (zh) 一种冷却装置及具有该冷却装置的封闭异氰酸酯生产设备
CN115452356A (zh) 一种用于空调的膨胀阀开度控制测试装置及其方法
JPH07185586A (ja) 回分式汚水処理装置及び活性汚泥濃度の計測装置
CN118269214B (zh) 一种无机生态石智能高效超声养护模块集成一体化设备
Schlumbach et al. Controlled sucrose crystallization at pilot-plant scale
JP3381023B2 (ja) 化学分析装置
JPH0587725A (ja) 粒度分布測定装置
CN211453246U (zh) 一种化妆品粘度检测仪
CN211988712U (zh) 一种实验室用恒温水槽
KR102175840B1 (ko) 냉간 압연의 압연유 농도 계측 시스템
CN221752979U (zh) 一种实验室树脂淋洗及反洗装置
CN113617225B (zh) 一种动物血清外源病毒的清理装置和方法

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV LY MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

DPEN Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed from 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2581850

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 07034701

Country of ref document: CO

WWE Wipo information: entry into national phase

Ref document number: 200580034751.4

Country of ref document: CN

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2005784657

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2007117709

Country of ref document: RU

WWP Wipo information: published in national office

Ref document number: 2005784657

Country of ref document: EP

ENP Entry into the national phase

Ref document number: PI0517544

Country of ref document: BR