Method of forming a three-dimensional object comprising additives imparting reduction of shrinkage to photohardenable compositions

• US 5,128,235 A
• Filed: 04/21/1989
• Issued: 07/07/1992
• Est. Priority Date: 04/21/1989
• Status: Expired due to Fees

• Current Assignee: Dsm Nv
• Original Assignee: E. I. du Pont de Nemours and Company (Corteva, Inc.)
• Inventors: Vassiliou, Eustathios, Grossa, Mario
• Primary Examiner(s): Bowers, Jr., Charles L.
• Assistant Examiner(s): CHU, JOHN S Y
• Application Number:
  US07/341,868
• Time in Patent Office: 1,173 Days
• Field of Search: 430/404, 430/323, 430/281, 430/253, 430/257, 430/271, 430/321, 430/911, 430/394, 430/269, 430/322, 430/907, 522/120, 525/308, 525/931, 427/54.1, 264/22
• US Class Current: 264/401
• CPC Class Codes: B29C 2035/0833 using actinic light
• CPC Class Codes: B29C 64/135 the energy source being concentrated, e.g. scanning lasers or focused light sources
• CPC Class Codes: G03F 7/0037 Production of three-dimensional images
• CPC Class Codes: G03F 7/027 Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds G03F7/075 takes precedence
• CPC Class Codes: G05B 2219/49013 Deposit layers, cured by scanning laser, stereo lithography SLA, prototyping
• CPC Class Codes: Y10S 430/108 Polyolefin or halogen containing

Abstract

Method of forming an integral three-dimensional object from a photohardenable liquid composition with low shrinkage containing a linear polymer which is soluble in the liquid but separates into a separate phase upon photohardening.

Claims

1. A method for accurately fabricating an integral three dimensional object from successive layers of a photohardenable liquid composition comprising the steps of:

(a) forming a layer of a liquid photohardenable liquid;

(b) photohardening at least a portion of the layer of photohardenable liquid by exposure to actinic radiation;

(c) introducing a new layer of photohardenable liquid onto the layer previously exposed to actinic radiation; and

(d) photohardening at least a portion of the new liquid layer by exposure to actinic radiation, with the requirement that the photohardenable composition comprises an ethylenically unsaturated monomer, a photoinitiator, and a linear polymer mixed therein selected from the group consisting of polystyrene, substituted polystyrene, alpha alkyl polystyrene, beta alkyl polystyrene, substituted alpha alkyl polystyrene, substituted beta alkyl polystyrene, and mixture thereof, the linear polymer being soluble in the composition but separating into a separate phase upon photohardening the composition, the linear polymer occupying a first volume in the absence of all other components of the composition, the photohardenable composition occupying a second volume in the absence of the linear polymer mixed therein, and the photohardenable composition containing the linear polymer occupying a third volume,

wherein the third volume is smaller than the sum of the first volume and the second volume.

2. The method of claim 1 wherein steps (c) and (d) are successively repeated.

3. The method as described in claim 1, wherein the separate phase of the photohardenable composition is in form of domains having an average diameter smaller than 250 micrometers, and wherein the separate phase has a volume constituting at least 10% of the total volume of the composition after photohardening.

4. The method as described in claim 1, wherein the additive compound is between 10% and 50% of the total photohardenable composition, by weight.

5. The method as described in claim 1, wherein the polymer has a number average molecular weight between 10,000 and 250,000.

6. The method as described in claim 1, wherein the polymer is a copolymer comprising a first monomer and a second monomer,

the first monomer corresponding to a homopolymer, which is soluble in the photohardenable composition before photohardening but separates into a second phase upon photohardening,

the second monomer corresponding to a homopolymer, which is soluble in the photohardenable composition both before and after photohardening.

7. The method as described in claim 1, wherein the polymer has ethylenical unsaturation, the ethylenical unsaturation having an equivalent weight between 1,000 and 5,000 grams per unsaturated site.