[go: up one dir, main page]

CN1012371B - Preparation method of coupling agent - Google Patents

Preparation method of coupling agent

Info

Publication number
CN1012371B
CN1012371B CN89102500A CN89102500A CN1012371B CN 1012371 B CN1012371 B CN 1012371B CN 89102500 A CN89102500 A CN 89102500A CN 89102500 A CN89102500 A CN 89102500A CN 1012371 B CN1012371 B CN 1012371B
Authority
CN
China
Prior art keywords
coupling agent
rcoo
composite material
atoms metal
polyvinyl chloride
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
CN89102500A
Other languages
Chinese (zh)
Other versions
CN1042722A (en
Inventor
辛树祥
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.)
Nanjing University
Original Assignee
Nanjing University
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 Nanjing University filed Critical Nanjing University
Publication of CN1042722A publication Critical patent/CN1042722A/en
Publication of CN1012371B publication Critical patent/CN1012371B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F279/00Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
    • C08F279/02Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
    • C08F279/04Vinyl aromatic monomers and nitriles as the only monomers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S525/00Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S525/932Blend of matched optical properties

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

In the formulation of polyvinyl chloride composite material (RCOO)aM(OX)b[ wherein R is a hydrocarbon group; m is a metal element; x is phosphoryl or sulfonyl]The single alkoxy titanate coupling agent has excellent compatibility and rheological property. The kind of the coupling agent to the inorganic fillerAnd the water content has no special requirement, and the cost is low. The tensile strength and the elongation of the composite material after molding are not lower than those of the composite material using the ND-102 coupling agent. The synthesis of such coupling agents is described.

Description

Manufacturing method of coupling agent
The invention belongs to the prescription of polyvinilchlaride compounds.
Often in the polyvinyl chloride (PVC) RESINS add mineral filler improving its mechanical property and to reduce the resin demand of goods, but the consistency of mineral filler and interlaminar resin is poor, after resin added mineral filler, the rheological that adds man-hour was little, brings difficulty to processing.Present prescription is to add single alkoxy type titanate coupling agent with the consistency of improving storeroom and the rheological that adds man-hour.This type of titanic acid ester contains a hydrolysising group (as isopropoxy), and therefore the water content to mineral filler has strict requirement, and the cost of single alkoxy type titanic acid ester is higher.
The object of the present invention is to provide a class to the mineral filler water content require undemanding, the prescription of lower-cost polyvinyl chloride composite materials.
The invention provides the prescription of polyvinilchlaride compounds, it is characterized in that with chemical formula (RCOO) aM(OX) bFor replacing titanic acid ester, the material of representing joins resin, in the batching of mineral filler or other auxiliary agent, to improve the consistency and the rheological that adds man-hour between the material.At formula (RCOO) aM(OX) bIn, the M central atom can be metallic elements such as Ca, Sr, Ba, Al, Sn, Pb, Mn, Fe, Ti, Zr, Sb, Bi, V, Cu, Cr, Co, Ni, Zn, Cd, R can be C 7-C 21Saturated or undersaturated alkyl or aromatic hydrocarbyl, X can be two different octyloxy phosphoryls
Figure 89102500_IMG2
, the dodecyl benzenesulfonyl or
Figure 89102500_IMG3
Group, b 〉=a, a 〉=0, and a+b=n, n is the Oxidation Number of atoms metal M.This type of material can be in the aqueous solution of pH=6-11, between the room temperature to 100 ℃, will be equivalent to M(OH) nCompound and RCOOH and di (isooctyl) phosphate effect make:
Figure 89102500_IMG4
Because (RCOO) aM(OX) bIn do not contain hydrolysising group, therefore kind and its water content of mineral filler are not all had particular requirement, and cost is more much lower than titanic acid ester.It improves the consistency of mineral filler and interlaminar resin, and rheological increases, at 1000 parts of CaCO 3With contain 5 parts (RCOO) in 1500 parts of mineral oil aM(OX) bThe time, the viscosity of system following (table is seen the literary composition back):
In this prescription,, can reduce or replace the consumption of thermo-stabilizer lead salt if add epoxy soybean oil.
Below further specify content of the present invention by specific embodiment.
Example 1 adds Fe in 500ml water 2O 380 restrain, and oleic acid 282 grams and di (isooctyl) phosphate 644 grams stir, and remove water layer in reaction under 80~90 ℃ after 1 hour, get C after the drying 17H 33COOFe- It is a brown solid, and fusing point is 110-124 ℃.
Example 2, in 500ml water, add Al 2(SO 4) 318H 2The O333 gram stirs, and adds NaHCO then 3, regulate pH=6~8, add oleic acid 282 grams, di (isooctyl) phosphate 644 grams stir, and remove water layer in reaction under 50~80 ℃ after two hours, are washed till no SO with deionized water 2- 4Exist, after the drying
Figure 89102500_IMG6
, it is a white solid, fusing point is 141.8~148 ℃.
Example 3, polyvinyl chloride composite materials prescription: PVC(three types) [production of Zhenjiang resin processing plant]: 100 parts; Lightweight CaCO 3(320 order all-pass are crossed) [making a leapleap forward and refine the production of grey factory in Nanjing]: 100 parts; Three salt: 5 parts; Lead stearate: 1 part; Barium stearate: 1.5 parts; DOP:20 part;
Figure 89102500_IMG7
: 1 part, after the batching, 198 ℃ of machine-shapings, its tensile strength laterally is 204.9kg/cm 2; Be 226.2kg/cm vertically 2(be respectively 202.1kg/cm with the ND-102 coupling agent 2And 238.9kg/cm 2), its elongation laterally is 10.0%; Vertically be 15.2%(ND-102 coupling agent difference 8.8% and 11.2%).
Sample blank Ca(OX) 2Zn(OX) 2Fe(OX) 3
Viscosity (centipoise) 15,000 600 600 680
C 17H 33COOFe(OX) 2ND-102
260 420

Claims (2)

1, a kind of coupling agent (RCOO) that is used for polyvinyl chloride composite materials aM (OX) b, wherein R can be C 7-C 21Saturated or unsaturated fatty hydrocarbons base or aromatic hydrocarbyl, M is an atoms metal, X is two different octyloxy phosphoryls , b≤a, a 〉=0, and a+b=n, n is the Oxidation Number of atoms metal M, it is characterized in that it can be in the aqueous solution of pH=6-11, between the room temperature to 100 ℃, by being equivalent to M (OH) nCompound and RCOOH and di (isooctyl) phosphate effect make.
2, coupling agent according to claim 1 (RCOO) aM(OX) b, it is characterized in that M can be Ca, Sr, Ba, Al, Sn, Pb, Mn, Fe, Ti, Zr, Sb, Bi, V, Cu, Co, Ni, Zn, Cd atoms metal.
CN89102500A 1985-04-01 1985-04-01 Preparation method of coupling agent Expired CN1012371B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN85102666.4A CN1005982B (en) 1985-04-01 1985-04-01 Recipe of polyvinilchlaride compounds

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
CN85102666.4A Division CN1005982B (en) 1985-04-01 1985-04-01 Recipe of polyvinilchlaride compounds
CN85102666 Division 1985-04-01

Publications (2)

Publication Number Publication Date
CN1042722A CN1042722A (en) 1990-06-06
CN1012371B true CN1012371B (en) 1991-04-17

Family

ID=4792667

Family Applications (2)

Application Number Title Priority Date Filing Date
CN85102666.4A Expired CN1005982B (en) 1985-04-01 1985-04-01 Recipe of polyvinilchlaride compounds
CN89102500A Expired CN1012371B (en) 1985-04-01 1985-04-01 Preparation method of coupling agent

Family Applications Before (1)

Application Number Title Priority Date Filing Date
CN85102666.4A Expired CN1005982B (en) 1985-04-01 1985-04-01 Recipe of polyvinilchlaride compounds

Country Status (1)

Country Link
CN (2) CN1005982B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69700223T2 (en) * 1996-04-30 1999-12-09 Samsung Electronics Co. Ltd., Suwon Circuit for regulating the speed of a rotary motor
CN102504335A (en) * 2011-12-19 2012-06-20 牟作峰 Preparation method of coupling agent

Also Published As

Publication number Publication date
CN85102666A (en) 1986-09-24
CN1042722A (en) 1990-06-06
CN1005982B (en) 1989-12-06

Similar Documents

Publication Publication Date Title
EP1958950A8 (en) Process for the preparation of dialkylphosphinic acid salts
EP0587831B1 (en) Overbased natural oils as additives for lubricants, plastics, paints, inks and greases
CA2026499A1 (en) Water-dispersible binder composition, a process for the production of a stoving filler and a coating prepared therefrom
CN1112916A (en) Process for the production of itaconic acid by fermentation
CA2533371A1 (en) Electroconductive powder and method for production thereof
EP0325030A3 (en) Polyamide resin compositions and laminates thereof
EP0447360A2 (en) Glycidylester of tricarboxylic acid adducts
CN1012371B (en) Preparation method of coupling agent
EP0175287A3 (en) Organophilic modified layered-silicic acid adsorbents
KR850001721A (en) Alkoxy Carbonylation or Carbonylation Process Using CO and Organohydroxyl Compounds
US3085100A (en) Oxyalkylated lecithin
CN85102660A (en) The prescription of a kind of polyethylene and polypropylene composite material
DE1943695B2 (en) Mixture of an epoxy resin with 1,2-epoxy groups and a curing agent
JPS6416809A (en) Metal-containing polymer composition and production thereof
CN105419147A (en) Formula of composite polyvinyl chloride material
CN1496414A (en) A method for removing calcium from zinc-treated sulfate solution
CN1144223A (en) Method for preparation of zinc dialkyl dithiophosphate
US6362265B1 (en) Additives with reduced residual tin content and thermoplastic compositions containing the same
US3271309A (en) Grease compositions
US2373387A (en) Tin soaps and preparation thereof
EP0759926B1 (en) Process for producing arabino-nucleosides
CN101130674A (en) Adhesion promotion agent of composite metal stearate
EP0131525A3 (en) Process for producing acidic compositions and acidic compositions obtained
US4497743A (en) Organosoluble salts of manganese, process of preparation of same
CN105295198A (en) Formula of polyethylene and polypropylene composite

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
C13 Decision
GR02 Examined patent application
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee