CN101144010A - Method for preparing acid-resistant pressing crack supporting agent - Google Patents

Method for preparing acid-resistant pressing crack supporting agent Download PDF

Info

Publication number
CN101144010A
CN101144010A CNA2007101680572A CN200710168057A CN101144010A CN 101144010 A CN101144010 A CN 101144010A CN A2007101680572 A CNA2007101680572 A CN A2007101680572A CN 200710168057 A CN200710168057 A CN 200710168057A CN 101144010 A CN101144010 A CN 101144010A
Authority
CN
China
Prior art keywords
supporting agent
compound
agent
barium
percent
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.)
Granted
Application number
CNA2007101680572A
Other languages
Chinese (zh)
Other versions
CN100535078C (en
Inventor
田小让
吴伯麟
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.)
Guilin University of Technology
Original Assignee
Guilin University of Technology
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 Guilin University of Technology filed Critical Guilin University of Technology
Priority to CNB2007101680572A priority Critical patent/CN100535078C/en
Publication of CN101144010A publication Critical patent/CN101144010A/en
Application granted granted Critical
Publication of CN100535078C publication Critical patent/CN100535078C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)

Abstract

The invention discloses a preparation method for acid fracturing resistant supporting agent, the raw material of which contains 60-85 percent by mass of alumina bauxite or refractory material waste material, 5-30 percent by mass of clay, 5-20 percent by mass of baric compound or witherite, 0-10 percent by mass of sintering agent; sintering agent is one or more of Fe2O3, TiO2, borax and magnetite, the specific procedure of the method is as follows: (1) the raw material is added into a ball mill device in proportion to ball mill; (2) the material from the step (1) can be granulated into partly finished particles; (3) the partly finished particles from the step (2) is sintered at 1300 DEG C-1400 DEG C for 1-3h, followed by free cooling to room temperature to get fracturing supporting agent with good acid resistance. The invention is based on present situation of commonly using alumina bauxite and high aluminum waste as main material in internal supporting agent production industry, which greatly improves the acid resistance of finished fracturing supporting agent through adding baric compound or witherite into the raw material to improve the batching.

Description

A kind of preparation method of acid-resistant pressing crack supporting agent
Technical field
The present invention relates to a kind of preparation method of acid-resistant pressing crack supporting agent.
Background technology
Fracturing propping agents are the important proprietary materials of oil, gas industry.Acid resistance is very important indexs of fracturing propping agents, and to fracturing effect, the flow conductivity of persistence that fracturing propping agents use and oil, gas has significant effects.Many industrial waste such as the high alumina refractories waste materials with bauxitic clay or high alumina of the fracturing propping agents that China produces are main raw material, and this type of raw material is Al 2O 3Porous ore structure, the fracturing propping agents acid resistance of producing is generally relatively poor, therefore the oil and gas industry standard SY/T5108-2006 that implemented on January 1st, 2007 decreases to the acid resistance of fracturing propping agents, but the sour solubility of domestic propping agent does not still generally reach this standard-required.
Summary of the invention
The objective of the invention is by improving batching, to improve the acid resistance of propping agent at the general higher present situation of the acid solubility of present homemade fracturing propping agents.
Raw materials quality per-cent of the present invention is: bauxitic clay or refractory waste 60-85%, clay 5-30%, the compound of barium or witherite 5-20%, sintering agent 0-10%.
Above-mentioned bauxitic clay or refractory waste are Al 2O 3The quality percentage composition is greater than 55% bauxitic clay or refractory waste; The compound of barium is the compound of the quality percentage composition of barium greater than 50% barium; Sintering agent is Fe 2O 3, TiO 2, a kind of in borax and the magnetite or several.
Concrete steps are:
(1) raw material is put into ball mill device by ratio of components and carry out ball milling;
(2) (1) step gained material is prepared into the work in-process particle through granulation;
(3) (2) step gained work in-process particle was carried out sintering 1-3 hour at 1300 ℃-1400 ℃, naturally cool to room temperature and can obtain the good fracturing propping agents of acid resistance.
According to testing by the SY/T5108-2006 recommend method, finished acid solubleness of the present invention has reached the requirement of industry standard between 3.0%-6.0%.
It is the present situation of main raw material with bauxitic clay and high aluminium waste generally that the present invention is based on domestic propping agent production industry, makes the acid resistance of fracturing propping agents finished product improve greatly by improving compound or the witherite that has particularly added barium in raw material of preparing burden.
Embodiment
Embodiment 1:
(1) raw materials quality per-cent is: refractory waste (taking from wuhan iron ﹠ steel croup co.) 75%, clay (picking up from Zhanjiang, Guangdong) 14%, titanium dioxide (chemical pure) 2%, barium carbonate (chemical pure) 9%; The chemical ingredients of refractory waste and clay is seen subordinate list 1 and subordinate list 2 respectively;
(2) raw material is put into ball mill device by ratio of components and carried out ball milling 24 hours;
(3) (2) step gained material is prepared into the work in-process particle through granulation;
(4) with (3) step gained work in-process particle in cabinet-type electric furnace 1350 ℃ carried out sintering 2 hours, naturally cool to room temperature and can obtain the good fracturing propping agents of acid resistance.
It is 8/16 purpose finished product that sieve is got a certain amount of particle size range, test by the SY/T5108-2006 recommend method, recording this finished acid solubleness is 4.4%, and antiacid dissolubility can reach the SY/T5108-2006 standard-required, is better than the market product of the same particle size range of being tested.
We are qualitative relatively finished product of the present invention and market producer product up to standard (8/16 order in the laboratory, percentage of damage is 10.8% under the 69Mpa locking pressure) anti-breaking capacity: the finished product of the present invention of equal in quality, same particle size scope and this producer's product are put into ball grinder, on ball mill with alumina ball polishing (impacting).The result shows that the anti-breaking capacity of finished product of the present invention is better than this producer's product.
Embodiment 2:
(1) raw materials quality per-cent is refractory waste (taking from wuhan iron ﹠ steel croup co.) 60%, clay (picking up from Zhanjiang, Guangdong) 26%, barium carbonate (chemical pure) 14%; The chemical ingredients of refractory waste and clay is seen subordinate list 1 and subordinate list 2 respectively;
(2) raw material is put into ball mill device by ratio of components and carried out ball milling 24 hours;
(3) (2) step gained raw material is prepared into the work in-process particle through granulation;
(4) with (3) step gained work in-process particle in cabinet-type electric furnace 1350 ℃ carried out sintering 2 hours, naturally cool to room temperature and can obtain the good fracturing propping agents of acid resistance.
Sieve is got the finished product that a certain amount of particle size range is 0.85-1.18mm (16/20 order), test by the SY/T5108-2006 recommend method, recording this finished acid solubleness is 4.6%, and antiacid dissolubility can reach the SY/T5108-2006 standard-required, is better than the market product of the same particle size range of being tested.
We are qualitative relatively finished product of the present invention and market producer product up to standard (8/16 order in the laboratory, percentage of damage is 10.8% under the 69Mpa locking pressure) anti-breaking capacity: the finished product of the present invention of equal in quality, same particle size scope and this producer's product are put into ball grinder, on ball mill with alumina ball polishing (impacting).The result shows that the anti-breaking capacity of finished product of the present invention is better than this producer's product.
The chemical constitution (mass percent) of subordinate list 1 wuhan iron ﹠ steel croup co. refractory waste
Al 2O 3 SiO 2 Fe 2O 3 TiO 2 CaO MgO
80.96 12.28 2.96 2.93 0.61 0.30
The chemical constitution (mass percent) of Zhanjiang, subordinate list 2 Guangdong clay
SiO 2 Al 2O 3 TiO 2 Fe 2O 3 MgO CaO K 2O Na 2O Burn vector
55.15 36.11 0.25 0.43 0.14 0.36 0.35 0.27 6.79

Claims (3)

1. the preparation method of an acid-resistant pressing crack supporting agent is characterized in that raw materials quality per-cent is: bauxitic clay or refractory waste 60-85%, clay 5-30%, the compound of barium or witherite 5-20%, sintering agent 0-10%; Sintering agent is Fe 2O 3, TiO 2, a kind of in borax and the magnetite or several;
Concrete steps are:
(1) raw material is put into ball mill device by ratio of components and carry out ball milling;
(2) (1) step gained material is prepared into the work in-process particle through granulation;
(3) (2) step gained work in-process particle was carried out sintering 1-3 hour at 1300 ℃-1400 ℃, naturally cool to room temperature and can obtain the good fracturing propping agents of acid resistance.
2. preparation method according to claim 1 is characterized in that described bauxitic clay or refractory waste are Al 2O 3The quality percentage composition is greater than 55% bauxitic clay or refractory waste.
3. preparation method according to claim 1, the compound that it is characterized in that described barium is the compound of the quality percentage composition of barium greater than 50% barium.
CNB2007101680572A 2007-10-30 2007-10-30 Method for preparing acid-resistant pressing crack supporting agent Expired - Fee Related CN100535078C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2007101680572A CN100535078C (en) 2007-10-30 2007-10-30 Method for preparing acid-resistant pressing crack supporting agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2007101680572A CN100535078C (en) 2007-10-30 2007-10-30 Method for preparing acid-resistant pressing crack supporting agent

Publications (2)

Publication Number Publication Date
CN101144010A true CN101144010A (en) 2008-03-19
CN100535078C CN100535078C (en) 2009-09-02

Family

ID=39206750

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2007101680572A Expired - Fee Related CN100535078C (en) 2007-10-30 2007-10-30 Method for preparing acid-resistant pressing crack supporting agent

Country Status (1)

Country Link
CN (1) CN100535078C (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101811873A (en) * 2010-04-08 2010-08-25 桂林理工大学 Method for preparing silicon-free or low-silicon acidproof ceramic fracturing propping agent
CN101575503B (en) * 2009-06-11 2011-08-31 邹平金刚新材料有限公司 High-strength fracturing propping agent for petroleum and preparation method thereof
CN101629075B (en) * 2009-08-14 2012-09-05 陕西省轻工业研究设计院 Oil fracturing proppant containing coal gangue
CN101717628B (en) * 2009-11-20 2013-02-20 三门峡方圆实业股份有限公司 Low-density ceramsite propping agent and preparation method thereof
CN103288428A (en) * 2013-05-16 2013-09-11 陕西科技大学 Method for preparing fracturing propping agent specially used for shale gas from poor bauxite
CN111454076A (en) * 2020-04-30 2020-07-28 西安建筑科技大学 Ceramsite proppant prepared from blast furnace tapping channel waste and preparation process

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102786921A (en) * 2012-08-03 2012-11-21 贵州林海陶粒制造有限公司 Low-density oil fracturing propping agent and preparation method thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101575503B (en) * 2009-06-11 2011-08-31 邹平金刚新材料有限公司 High-strength fracturing propping agent for petroleum and preparation method thereof
CN101629075B (en) * 2009-08-14 2012-09-05 陕西省轻工业研究设计院 Oil fracturing proppant containing coal gangue
CN101717628B (en) * 2009-11-20 2013-02-20 三门峡方圆实业股份有限公司 Low-density ceramsite propping agent and preparation method thereof
CN101811873A (en) * 2010-04-08 2010-08-25 桂林理工大学 Method for preparing silicon-free or low-silicon acidproof ceramic fracturing propping agent
CN103288428A (en) * 2013-05-16 2013-09-11 陕西科技大学 Method for preparing fracturing propping agent specially used for shale gas from poor bauxite
CN103288428B (en) * 2013-05-16 2014-07-02 陕西科技大学 Method for preparing fracturing propping agent specially used for shale gas from poor bauxite
CN111454076A (en) * 2020-04-30 2020-07-28 西安建筑科技大学 Ceramsite proppant prepared from blast furnace tapping channel waste and preparation process

Also Published As

Publication number Publication date
CN100535078C (en) 2009-09-02

Similar Documents

Publication Publication Date Title
CN100535078C (en) Method for preparing acid-resistant pressing crack supporting agent
CN101085914B (en) Method for preparing acid-resistant pressing crack supporting agent from red mud
CN100413782C (en) Method of preparing high-purity ultra-fine sphere silicon micro-powder
CN112028637A (en) Preparation method of high-reliability long-life silicon nitride ceramic ball for aviation bearing
CN107840658B (en) Preparation method of zirconia ceramic with high fracture toughness
CN103080027A (en) Chromium oxide powder
CN106746772B (en) Preparation method of calcium titanium aluminate hollow spheres produced by utilizing ferrotitanium slag
CN105294138A (en) Doublet aluminum oxide micropowder and preparation method thereof
WO2022062293A1 (en) High-performance energy-saving magnesium-based raw material and preparation method therefor
CN101298383A (en) Method for improving acid resistant property of porcelain granule fracturing propping agent
CN108395220A (en) A kind of preparation method of the wear-resisting diphase ceramic material of aluminium oxide-zirconium oxide
US20210284579A1 (en) Titanium-containing calcium hexaaluminate material and preparation method thereof
CN101811873A (en) Method for preparing silicon-free or low-silicon acidproof ceramic fracturing propping agent
CN107245621A (en) A kind of wear-and corrosion-resistant molybdenum alloy and preparation method thereof
CN111362708A (en) Refractory material for smelting titanium-aluminum alloy and preparation method thereof
CN113800895A (en) Wear-resistant zirconium-aluminum composite ball and preparation method thereof
CN104045325A (en) Preparation method of self-lubricating cutter material added with coated calcium fluoride powder
CN106673626A (en) Low-cost alumina powder material for producing self-toughened wear-resistant alumina ceramic
CN115093217A (en) Preparation method of gray zirconia ceramic and gray zirconia ceramic
CN108191235A (en) A kind of Bone China Glaze, glaze slip and preparation method
CN102093878A (en) Calcium aluminate acidproof ceramic fracturing propping agent and preparation method thereof
CN101555148A (en) High strength acid resistant refractory brick and preparation method thereof
CN112094125B (en) Low-thermal-conductivity low-thermal-expansion magnesium-based raw material and preparation method thereof
JP4949657B2 (en) High wear-resistant zirconia microspheres and production method thereof
Sun et al. Effect of cobalt on properties of vitrified bond and vitrified cubic boron nitride composites

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C56 Change in the name or address of the patentee
CP03 Change of name, title or address

Address after: 541004 Guilin city of Guangxi Road No. 12 building of Guilin University of Technology

Patentee after: Guilin University of Technology

Address before: 541004 Guilin city of the Guangxi Zhuang Autonomous Region Road No. 12 building of Guilin University of Technology

Patentee before: Guilin University of Technology

EE01 Entry into force of recordation of patent licensing contract

Assignee: China Ceramic Proppant (Guizhou) Ltd.

Assignor: Guilin University of Technology

Contract record no.: 2012520000011

Denomination of invention: Method for preparing acid-resistant pressing crack supporting agent

Granted publication date: 20090902

License type: Exclusive License

Open date: 20080319

Record date: 20120713

CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090902

Termination date: 20171030