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ANCAMIDE® A. Technical Datasheet | Supplied by Evonik. Standard reactive liquid polyamide. Acts as a curing agent for epoxy resins. Possesses low. Ancamide® A by Evonik is a liquid polyamide. Acts as curing agent for epoxy resins. Used in encapsulation and castings. Offers low. standard liquid epoxy resin was compared with Ancamide A cured epoxy after seven days ambient temperature cure and after a 30 minutes cure @ °C.

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Skip to main content. Log In Sign Up. Safety information on the handling Safe Handling and Storage Manual of novolac resins, epoxy resins, solvents, Form No. Formulators-customers Department or your Dow sales representative. Companion bulletins, All rights reserved. They exhibit little shrinkage applications. Good epoxy resins are designed to overcome Similar commercial success has been resistance to a variety of chemicals many of the specific disadvantages of earned by the families of D.

They and solution epoxy resins, flexible results with properly cured are compatible with practically all other epoxy resins, brominated epoxy resins, formulations. They accept a mixing. Because they are true epoxy D.

Cured formulations modifiers, an almost unlimited range and exhibit good hardness, impact Table 1 on page 4 lists the typical variety of properties may be obtained. The tenacity of epoxy Table 2 lists the typical properties of This bulletin describes the bisphenol A- adhesion to almost any surface two liquid epoxy resins that contain a based liquid epoxy resins and aliphatic is without equal among organic reactive diluent a CC14 aliphatic glycol epoxy resins offered by Dow.

Each resin anamide briefly epoxy-related products may be ancamixe curing conditions. Prior to handling any of these resins, i. This is also true of epoxy, poly- positions having rather low impact and from your supplier s adequate information ester, phenolic, and melamine resins. There are pertaining to safe operations for your workers However, liquid epoxy resins, because many approaches ancamude improving these and your plant. Request Material Safety Data of their structure and the method of properties and increasing flexibility in MSD sheets for each product from its their cure, are superior to these other epoxy resin systems.

Among them are supplier. Dow flexible epoxy tionally low viscosity and resins are principally used as additives D. Under certain conditions, liquid epoxy resins may crystallize. Crystallization may take D. The pure digly- the material or on the container.

Occasionally, A formulated blend of D. The occurrence of crystalliza- a low viscosity product. Crystallization may be induced tion is in no way an indication that an epoxy resin utility in filled formulations for flooring by chilling, seeding by dust particles, or is contaminated or out of specification.

Ancamide® A Curing Agent by Evonik Resource Efficiency GmbH, BL Crosslinkers – Paint & Coatings

Rather, it is a phenomenon which can occasionally occur compounds, grouts, adhesives, incorporation of filler. Warming to during storage at room temperature or below. Long-term warm storage Material that shows evidence of crystallization to diluent.


This temperature should be maintained until dissolution occurs. If steam is cidyl ether.

Used in same applications as weight bisphenol A semi-solid epoxy used, it should be circulated around tightly D.

Used in adhesives and coatings or closed containers which have been assembled as a modifier for other epoxy resins to under a tarpaulin. Also, for further information A low epoxide equivalent weight liquid and adhesion. BoxMidland, MID. A general purpose, widely used liquid the unique characteristic of crystalliza- Crystallization is chiefly a result of the purity resin.

It is recognized as a standard from tion resistance. Factors that may encourage D. To discourage crystallization, store epoxy resins at room temperature or higher. Because of its high purity and equivalent to those of D.

Ancamide® 350A Curing Agent

Liquid epoxy resins are converted through these reactive epoxy sites into tough, insoluble, and infusible solids. The simplest possible epoxy resin derived from the reaction of bisphenol A and epichlorohydrin is 2,2-bis[4- 2’3′ epoxy propoxy phenyl] propanecommonly called the diglycidyl ether of bisphenol A DGEBA. This group can react at higher temperatures with anhy- drides, organic acids, amino resins, and phenolic resins, or with epoxide groups when catalyzed to give additional cross-linking.

Each primary amine they assist in opening the epoxide Many commercial materials are suitable group is theoretically capable of reacting ring. Alcoholic or phenolic hydroxyls as reactive cross-linking agents for liq- with two epoxide groups, and each sec- accelerate the primary and secondary uid epoxy resins. The most common ondary amine group is capable of react- amine cures and thus provide for the types of curing agents are: Also used are adducts of the OH above amines with epoxy resins, dilu- Theoretically, the hydroxyls formed ents, or other amine-reactive com- should be capable of reacting with epoxy pounds.

Room temperature cures are groups to form an ether linage: Elevated O temperature cures are usually employed. However, the tertiary amine formed by the epoxy-secondary amine reaction is apparently too immo- bile and sterically hindered to act as a catalyst.

To calculate the Amine H equivalent resistance, and cure at ambient or mod- weight, use the following equation: Total weight includes all materials, erately elevated temperatures.

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Good both reactive and nonreactive. MW of amine a,b,c, etc. Pot life is short are characterized by an epoxy ring. Aromatic Polyamines parts D. To calculate the stoichiometric ratio of parts D. Cured systems give excellent perfor- Frequently, epoxy resins are blended, a useful feature for encapsulation and filled, or modified with reactive and potting. It is then necessary to adjust the concentration Calculation of Stoichiometric Ratios of the curing agent to cure only the To obtain optimum properties with poly- portion of the mix that is reactive; functional epoxide-reactive curing e.

This may be simply done desirable to react the resin and the cur- by calculating the epoxide equivalent ing agent at approximately stoichiometric weight EEW of the total mix and quantities. To determine the ratio then applying equation 2 to deter- required, calculations can be made as mine the amount of curing agent to add to parts of formulation.


May blush under humid conditions. Lower vapor pressure than D. Similar in properties to D. Lower vapor pressure and less critical adduct ratios offer improved handling characteristics. Can be used to make eutectic mix. Used in laminates, castings, and filament winding.

Diamino diphenyl 57 Has good B-stage shelf life. The opening of the anhydride ring At low elevated temperature cures, the Liquid and solid anhydrides are with an alcoholic hydroxyl to form ether and ester reactions take place at extensively used to cure epoxy resins.

At higher tempera- Products typical of this class are shown tures, the ester linkage occurs more O O in Table 6. An accelerator, usual- O O temperatures. Since reaction 3 can take ly a tertiary amine, is often used 0.

The opti- boxylic groups react with the epoxide the ratio of anhydride to epoxy is less mum amount is usually critical, depending to give an ester linkage: It can vary upon the anhydride and resin used and O from 0. O O tion should be determined experimentally.

Import Data and Price of ancamide under HS Code | Zauba

Elevated temperature O OH cures are necessary and long post cures The reaction of anhydrides with epoxy 3. The epoxide groups react with nascent are required to develop ultimate proper- groups is complex, with several compet- or existing hydroxyl groups, catalyzed ties. Electrical and physical strength ing reactions capable of taking place. Used in potting, filament windings, and clear castings. Reacts rapidly at high temperatures. Imparts flexibility to cured composition.

Low exotherm anhydride PA and long pot life. Used in large encapsulations. Similar to anhydride THPA hexahydrophthalic anhydride in cured resin properties.

Ancamire in pottings and encapsulations. Polyamides The reactivity of polyamides with without blushing and show outstanding This class of compounds can be consid- epoxies is similar to that of the aliphatic adhesion.

Formulations are high in vis- ered as modified polyfunctional aliphatic amines. Since the polyamides are cosity and are sometimes incompatible amines, since the polyamides most relatively large polymers, the ratio of with the resin until reaction anxamide been widely used are the condensation polyamide to epoxy is less critical than initiated.

They are usually dark in color. It Polyamide systems lose structural difunctional amine such as ethylenedi- is varied quite broadly to obtain proper- strength and insulation value rapidly amine. Their theorized structure is ties from hard to semi-flexible. In this with increasing temperatures, and are represented as follows: Semi-solid polyamide resin used primarily as a solvent cut solution Ancamide 2 to cure intermediate-molecular-weight epoxy resins in coating applications.

Also available in nacamide. Can be used to cure resins on wet substrates. Used in laminates, adhesives, potting, sealants, and coatings.

Also available in solution. Used in wet lay-ups, adhe- sives, potting, sealants, coatings, epoxy mortars, and tooling.