WO2010029387A1 - A method for production of a nano-reinforced material - Google Patents

A method for production of a nano-reinforced material Download PDF

Info

Publication number
WO2010029387A1
WO2010029387A1 PCT/IB2008/053662 IB2008053662W WO2010029387A1 WO 2010029387 A1 WO2010029387 A1 WO 2010029387A1 IB 2008053662 W IB2008053662 W IB 2008053662W WO 2010029387 A1 WO2010029387 A1 WO 2010029387A1
Authority
WO
WIPO (PCT)
Prior art keywords
nano
polyamide
production
reinforced material
fiberglass
Prior art date
Application number
PCT/IB2008/053662
Other languages
English (en)
French (fr)
Inventor
Idris Kaynak
Original Assignee
Idris Kaynak
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 Idris Kaynak filed Critical Idris Kaynak
Priority to TR2011/02309T priority Critical patent/TR201102309T1/tr
Priority to PCT/IB2008/053662 priority patent/WO2010029387A1/en
Publication of WO2010029387A1 publication Critical patent/WO2010029387A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/203Solid polymers with solid and/or liquid additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2377/00Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/40Glass

Definitions

  • the present invention relates to a nano-reinforced material with steel and ceramic characteristics produced by using polyamide, fiberglass and polyamide aminopropyl silane (PA-GMA) and a method for production of the said material.
  • PA-GMA polyamide, fiberglass and polyamide aminopropyl silane
  • Masses of the chemical materials used in the inventive polymer supported material and method for production of the said material are lighter than the materials used in the prior art due to their structure and to the interface process transition employed, and their mechanical properties are improved.
  • the objective of the present invention is to realize a nano-reinforced material having physical properties similar to steel or ceramics according to preference by using various polymer, fiberglass and nano-combining materials.
  • Another objective of this invention is to realize a method for production of a nano- reinforced material with the same chemical properties by reduced production costs.
  • Figure 1 is a view of the flow chart of the method for production of the inventive nano-reinforced material.
  • the present invention relates to a new production method recommended for production of a nano-reinforced material by using polyamide, fiberglass and polyamide aminopropyl silane (PA-GMA).
  • PA-GMA polyamide, fiberglass and polyamide aminopropyl silane
  • the said materials should individually wait at the waiting stations at predetermined temperatures and for predetermined periods before production, and are waited depending on the treatment period in order to be freed from the undesired substances present in their structures (101). They are retained stepwise in different stations preferably for 8 to 12 hours at a temperature of 90 to 100 0 C.
  • polyamide, fiberglass and polyamide aminopropyl silane are processed by filtered dry and warm air coming from outside.
  • the polyamide, fiberglass and polyamide aminopropyl silane (PA-GMA) which are cleaned from the undesired substances therein in sterilized media, and which will be transferred to the machine where combining process will take place after the determined period expires, are subjected to centrifuging before entering into the machine in order to attain a homogenous structure (102).
  • the mixture, that attains a homogenous structure enters into the machine where the combining process will be realized.
  • the mixture in the machine is primarily subjected to the heat treatment (103).
  • the purpose here is to bring polyamide and polyamide aminopropyl silane (PA-GMA) that is the nano-combining material, to a viscosity at which they will be able to melt and combine. While polyamide melts at around 300 0 C, the polyamide aminopropyl silane (PA-GMA) that is used as nano-combining material melts at approximately 28O 0 C. Then, among the elements present in the mixture, firstly the polyamide aminopropyl silane (PA-GMA) that is the nano-combining element melts and later polyamide melts. Since melting temperature of the fiberglass provided in the mixture is approximately 600-650 0 C, rigidity of the said fiberglass does not deteriorate.
  • PA-GMA polyamide and polyamide aminopropyl silane
  • the polyamide, polyamide aminopropyl silane (PA-GMA) and fiberglass which are at a viscosity suitable for the combination, are combined at a high temperature (104) and molded and cooled to obtain nano-reinforced material (105).
  • step (105) After being combined under high temperature and pressure (104), the mixture is cooled step by step (105).
  • cooling is realized by gradually reducing temperature values. This is because in order to ensure homogenous orientation within the material, temperature should not be decreased in an instant, but the desired temperature value should be reached by step by step cooling and solidification.
  • the molds should be at a certain temperature during molding process (105). This temperature value is preferably 80 to 9O 0 C.
  • the fiber glass used in the inventive method for production of a nano-reinforced material ensures that the modulus of elasticity of the newly formed material is more compared to the polyamide used as polymeric material, whereby it makes the nano- reinforced material more rigid.
  • modulus of elasticity of the nano-reinforced material realized with the above described production is measured to be approximately 21 GPa. Since modulus of elasticity of aluminum titanate (A12TiO5) which is known in the art with its ceramic characteristics is known to be 5 to 35 GPa, the nano-reinforced material produced according to the above mentioned method has ceramic characteristics due to 50 - 60% aluminum titanate.
  • the material when used in high temperatures the material does not undergo the problems that polyamide does at high temperatures when used alone; the fiberglass within the material acts as a ceramic and eliminates heat. Furthermore, the fact that the fiberglass inserted in the material during production is ensured to be distributed optimally in all directions ensures that the modulus of elasticity are close to each other in all three dimensions; and it is observed that the feature of modulus of elasticity of the nano- reinforced material resulting at the end of the production has increased. Thus, when hydrostatic force is applied to the nano-reinforced material it is aimed that the material exhibits the same behavior in all directions until the flow limit.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Reinforced Plastic Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
PCT/IB2008/053662 2008-09-11 2008-09-11 A method for production of a nano-reinforced material WO2010029387A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
TR2011/02309T TR201102309T1 (tr) 2008-09-11 2008-09-11 Bir nano takviyeli malzeme üretim yöntemi.
PCT/IB2008/053662 WO2010029387A1 (en) 2008-09-11 2008-09-11 A method for production of a nano-reinforced material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/IB2008/053662 WO2010029387A1 (en) 2008-09-11 2008-09-11 A method for production of a nano-reinforced material

Publications (1)

Publication Number Publication Date
WO2010029387A1 true WO2010029387A1 (en) 2010-03-18

Family

ID=40669465

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2008/053662 WO2010029387A1 (en) 2008-09-11 2008-09-11 A method for production of a nano-reinforced material

Country Status (2)

Country Link
TR (1) TR201102309T1 (tr)
WO (1) WO2010029387A1 (tr)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3498872A (en) * 1969-01-21 1970-03-03 Union Carbide Corp Glass fiber reinforced polyamide resin article and process therefor
JPS62225548A (ja) * 1986-03-27 1987-10-03 Nippon Glass Fiber Co Ltd ガラス繊維サイジング剤組成物
US5240974A (en) * 1990-07-05 1993-08-31 Degussa Aktiengesellschaft Polyamide reinforced with silanized glass fibers
US20010047050A1 (en) * 2000-04-14 2001-11-29 Hiroshi Oyamada Glass fiber reinforced polyamide resin composition
US20070286999A1 (en) * 2006-06-13 2007-12-13 Jacob Cornelis Dijt Sizing composition for glass fibers, sized fiber glass products, and composites

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3498872A (en) * 1969-01-21 1970-03-03 Union Carbide Corp Glass fiber reinforced polyamide resin article and process therefor
JPS62225548A (ja) * 1986-03-27 1987-10-03 Nippon Glass Fiber Co Ltd ガラス繊維サイジング剤組成物
US5240974A (en) * 1990-07-05 1993-08-31 Degussa Aktiengesellschaft Polyamide reinforced with silanized glass fibers
US20010047050A1 (en) * 2000-04-14 2001-11-29 Hiroshi Oyamada Glass fiber reinforced polyamide resin composition
US20070286999A1 (en) * 2006-06-13 2007-12-13 Jacob Cornelis Dijt Sizing composition for glass fibers, sized fiber glass products, and composites

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 198745, Derwent World Patents Index; AN 1987-317636, XP002530339 *

Also Published As

Publication number Publication date
TR201102309T1 (tr) 2012-02-21

Similar Documents

Publication Publication Date Title
KR101798255B1 (ko) 열방성 액정 중합체의 성형 및 이로부터 제조된 용품
JP5457032B2 (ja) 多孔質材料及びそれを製作する方法
KR101483740B1 (ko) 비대칭성 폴리비닐리덴플루오라이드 중공사막의 제조방법 및 이로부터 제조된 중공사막
CN108527868A (zh) 3d打印工件的热处理方法
EP2621712B1 (en) Polymer powder composition
CN111286074A (zh) 聚乳酸/纳米羟基磷灰石复合材料及其制备方法和应用
CN112771118A (zh) 包含第一聚酰胺组分(pa1)和第二聚酰胺组分(pa2)的烧结粉末(sp),其中第二聚酰胺组分(pa2)的熔点高于第一聚酰胺组分(pa1)的熔点
JP5096164B2 (ja) 造型複合材料
RU2692368C2 (ru) Смесь полиамидов с улучшенной текучестью
WO2010029387A1 (en) A method for production of a nano-reinforced material
JP5471338B2 (ja) 炭素長繊維強化ポリアミド複合材料
CN109749373B (zh) 一种改性液晶聚酯树脂复合物及其制备方法
CN113663522B (zh) 一种中空纤维膜膜丝的浇铸方法
JP2010235774A (ja) 炭素長繊維強化ポリプロピレン複合材料
JP5402584B2 (ja) 炭素長繊維強化ポリアミド複合材料
JP2013534505A (ja) セラミック素材用のセラミック材料の製造方法
JPH05194847A (ja) 現場複合成形品製造用の重合体組成物
US20210061961A1 (en) Composition for Preparing Polyamide Powders
CN110961636B (zh) 一种用于纺丝组件的烧结金属过滤芯及其制备方法
JP4040991B2 (ja) 芯材入りポリアミド樹脂成形体およびその製造方法
JPWO2022075249A5 (tr)
JP6160095B2 (ja) 炭素繊維強化熱可塑性樹脂プリプレグシートまたは成形品
CN1637068A (zh) 碳纤维增强杂萘联苯聚醚酮或杂萘联苯聚醚砜复合材料
CN109971996B (zh) 一种能有效提高塑性性能的TiB颗粒增强Ti基复合材料
Chik et al. Properties and morphology of injection moulded liquid crystalline polymer/polycarbonate blends

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08807597

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2011/02309

Country of ref document: TR

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 08807597

Country of ref document: EP

Kind code of ref document: A1