USH1807H - Organic pre-etch treatment for metal plating of cyclic olefin polymers - Google Patents
Organic pre-etch treatment for metal plating of cyclic olefin polymers Download PDFInfo
- Publication number
- USH1807H USH1807H US09/113,331 US11333198A USH1807H US H1807 H USH1807 H US H1807H US 11333198 A US11333198 A US 11333198A US H1807 H USH1807 H US H1807H
- Authority
- US
- United States
- Prior art keywords
- metal plating
- cyclic olefin
- plating
- etch
- olefin polymers
- 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.)
- Abandoned
Links
- 238000007747 plating Methods 0.000 title claims abstract description 15
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 14
- 239000002184 metal Substances 0.000 title claims abstract description 14
- 229920000089 Cyclic olefin copolymer Polymers 0.000 title claims abstract description 4
- 239000003960 organic solvent Substances 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims abstract description 7
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 5
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims abstract description 4
- 238000007654 immersion Methods 0.000 claims description 11
- 229920000642 polymer Polymers 0.000 claims description 6
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229920001187 thermosetting polymer Polymers 0.000 claims description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract description 12
- -1 poly(dicyclopentadiene) Polymers 0.000 abstract description 10
- 238000005530 etching Methods 0.000 abstract description 9
- 229910052759 nickel Inorganic materials 0.000 abstract description 7
- 230000008021 deposition Effects 0.000 abstract description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract description 2
- 239000008096 xylene Substances 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 description 12
- 229920003023 plastic Polymers 0.000 description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000008367 deionised water Substances 0.000 description 5
- 229910021641 deionized water Inorganic materials 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000007772 electroless plating Methods 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- CVNKFOIOZXAFBO-UHFFFAOYSA-J tin(4+);tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Sn+4] CVNKFOIOZXAFBO-UHFFFAOYSA-J 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- CAHQGWAXKLQREW-UHFFFAOYSA-N Benzal chloride Chemical compound ClC(Cl)C1=CC=CC=C1 CAHQGWAXKLQREW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000694440 Colpidium aqueous Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000000454 electroless metal deposition Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 229920003247 engineering thermoplastic Polymers 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- ZMLDXWLZKKZVSS-UHFFFAOYSA-N palladium tin Chemical compound [Pd].[Sn] ZMLDXWLZKKZVSS-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920000379 polypropylene carbonate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/18—Pretreatment of the material to be coated
- C23C18/20—Pretreatment of the material to be coated of organic surfaces, e.g. resins
- C23C18/22—Roughening, e.g. by etching
- C23C18/26—Roughening, e.g. by etching using organic liquids
Definitions
- a "direct metallization" process can be used, which eliminates the electroless plating step.
- Such a process has been developed by Atotech and is called Futuron®.
- Futuron® it is known to chemically etch prior to the direct deposition of the metal.
- the surfaces of some plastics are more difficult to etch than others.
- immersion of such plastics in a particular type of organic solvent prior to etching will make the plastic surface easier to etch and will sometimes improve the uniformity of the etching step.
- the organic solvent where effective, causes the plastic to swell at the surface, thus creating or opening microscopic pores or fissures, thereby facilitating the acid's access to the plastic.
- the organic solvent can be used undiluted or in admixture with another liquid with which it is miscible, e.g., water. Such a step is often referred to as an organic pre-etch step.
- organic pre-etch step has been reported for metal plating engineering thermoplastic resins such as ABS-PC, polysulfone, polyetherimide, polycarbonate, polyphenyleneoxide, polyoxymethylene, etc., as well as for thermoset resins such as the epoxies.
- Organic solvents that have been used for pre-etching include alcohols, ketones, lactones, aliphatic and aromatic hydrocarbons, and amines.
- acetone polypropylene carbonate
- methyl ethyl ketone butyrolacetone
- aiacetylmethane cresol
- heptane tetrahydrofuran
- ethylacetate dimethylformamide
- dioctylphthalate dipropylamine, quinoline, pyridine, etc.
- Such dicyclopentadiene polymers sometimes contain one or more comonomers such as ethylidene norbornene or tricyclopentadiene, and they may contain other additives such as one or more elastomers, inorganic particles, pigments, antioxidants, and surfactants.
- the use of an organic pre-etch step in the metal plating of cyclic olefin polymers has now been found to be beneficial in the swelling of the surface of such polymers and, as such, is expected to improve the efficiency and uniformity of etching in the same way it has aided the etching of other plastics.
- the temperature of the pre-etch treatment bath and the duration of the immersion therein will preferably be sufficient to cause a weight increase by swelling (absorption of the solvent) in the range of about 0.1 to 70 percent, and more preferably between about 0.1% and about 5%.
- the solvent is comprised of one or more compounds selected from the group consisting of aromatic hydrocarbons (including halogenated aromatic hydrocarbons) and halogenated aliphatic hydrocarbons.
- a copolymer of 95% dicyclopentadiene and 5% ethylidene norbornene when immersed for 5 minutes in toluene at room temperature, showed a weight gain swell of 2.9% and a fine uniform micro-etch of the surface.
- Immersion of the same polymer in 111-trichloroethane showed a swell of 4.9% after 5 minutes at 40° C.
- swelling was 63.5% and 7.6%, respectively, and heavy microporosity was evident on the surface.
- the preferred organic pre-etch solvent will have a solubility parameter near that of the polymer.
- a solubility parameter in the range of 9.3 to 11 e.g., from 9.6 to 10
- cal 0.5cm 1.5 was found to have the most swelling power.
- Condiriser SP is a cationic wetting agent sold by Okuno Chemical Company, of Japan. It serves to place a negative charge on the surface of the etched part, which promotes the attraction of the positively charged palladium ions during the treatment with the chemical activator, described next.
- Chemical activation of the etched part surface is accomplished by immersion for 5 minutes in a room temperature aqueous bath containing a palladium/tin hydrosol, Enplate Activator 850 (at a Pd/Sn concentration of 2%) and hydrochloric acid (at a concentration of 150 ml/l). This serves to deposit palladium ions on the etched surface. After several rinses in deionized water, the part is then immersed in a bath of dilute sulfuric acid at 40° C. for 8 minutes. The bath contains about 100 ml of sulfuric acid per liter of water. This treatment serves to remove excess hydrolyzed tin hydroxide from the deposits of palladium on the part surface, so that the tin hydroxide will not inhibit the deposition there of the plating metal, in the next step.
- electroless deposition of nickel on the etched part surface is accomplished by immersion for 5 minutes in a nickel plating bath at 40° C.
- the bath having a pH of 8.5, is a 20 volume percent solution of Enplate®n Ni-429 in deionized water.
- Enplate Ni-429 like Enplate Activator 850, is sold by Enthone-OMI.
- Enplate Ni-429 is an alkaline, electroless nickel solution.
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemically Coating (AREA)
Abstract
The process of metal plating an object formed out of a cyclic olefin polymer is improved by first immersing the object in an organic solvent, such as an aromatic hydrocarbon or a halogenated aliphatic hydrocarbon, that serves to swell the object at its surface, for example sufficiently to increase its weight by about 0.1 to 70%. In this way objects molded out of, for example, poly(dicyclopentadiene) can be pre-etched by being immersed in xylene for 5 minutes at room temperature, and then plated by the electroless deposition of nickel on the surface of the etched part. The pre-etching facilitates adhesion of the plating metal to the surface.
Description
It is common in the process of metal plating plastics with copper, nickel, chrome or other metals to first chemically etch the surface of the plastic to form a microscopic texture on the surface that facilitates adhesion of the metal to the surface. This etching step is usually followed by the application of an activator such as a palladium-tin colloid, followed by electroless metal deposition. Such processes are described in Standards and Guidelines for Electroplated Plastics, published by the American Society of Electroplated Plastics; in Chapter 12 of Ni and Cr Plating by J. K. Dennis and T. E. Such (1972); in "Electroplating of Plastics in Theory and Practice" by Heymann, Riedel, and Woldt in Angew. Chem. Int. Ed., Vol. 9, (1970), pp 425-433; and in "Practical Formulations for Plating on ABS Plastics in Metal Finishing, March 1986, pp. 51-54, all of which are incorporated herein by reference.
Alternatively, a "direct metallization" process can be used, which eliminates the electroless plating step. Such a process has been developed by Atotech and is called Futuron®. Here, too, it is known to chemically etch prior to the direct deposition of the metal.
The surfaces of some plastics are more difficult to etch than others. Sometimes immersion of such plastics in a particular type of organic solvent prior to etching will make the plastic surface easier to etch and will sometimes improve the uniformity of the etching step. Generally it is believed that the organic solvent, where effective, causes the plastic to swell at the surface, thus creating or opening microscopic pores or fissures, thereby facilitating the acid's access to the plastic. The organic solvent can be used undiluted or in admixture with another liquid with which it is miscible, e.g., water. Such a step is often referred to as an organic pre-etch step. This pre-etch step has been reported in Ni and Cr Plating by Dennis and Such (1972, pg 289); Electroless Plating: Fundamentals & Applications (1990) Chapter 14, pg 382-383; Plating of Plastics: Recent Developments, Chemical Technology Review, No. 138, published by the Noyes Corporation in 1979; and U.S. Pat. Nos. 3,769,061, 3,445,350, 3,479,160, 3,963,590, 3,905,877, 3,898,126, and 3,758,332, all of which are incorporated herein by reference.
The benefits of such an organic pre-etch step have been reported for metal plating engineering thermoplastic resins such as ABS-PC, polysulfone, polyetherimide, polycarbonate, polyphenyleneoxide, polyoxymethylene, etc., as well as for thermoset resins such as the epoxies. Organic solvents that have been used for pre-etching include alcohols, ketones, lactones, aliphatic and aromatic hydrocarbons, and amines. Specific examples of such include acetone, polypropylene carbonate, methyl ethyl ketone, butyrolacetone, aiacetylmethane, cresol, heptane, tetrahydrofuran, ethylacetate, dimethylformamide, dioctylphthalate, dipropylamine, quinoline, pyridine, etc.
When considering which compound to use for the organic pre-etch step, preference should be given to those solvents having a low boiling point and low vapor pressure, high flash point, low toxicity, low corrosivity, low purchase price, low disposal cost and effectiveness in swelling the polymer.
Thermoset polymers formed substantially from the ring-opening, metathesis catalyzed polymerization (ROMP) of cyclic olefins, e.g., dicyclopentadiene, have been commercially etched and plated for several years, as reported in JETRO, January 1994, pp. 38-39, incorporated herein by reference. Such dicyclopentadiene polymers sometimes contain one or more comonomers such as ethylidene norbornene or tricyclopentadiene, and they may contain other additives such as one or more elastomers, inorganic particles, pigments, antioxidants, and surfactants.
The use of an organic pre-etch step in the metal plating of cyclic olefin polymers has now been found to be beneficial in the swelling of the surface of such polymers and, as such, is expected to improve the efficiency and uniformity of etching in the same way it has aided the etching of other plastics. The temperature of the pre-etch treatment bath and the duration of the immersion therein will preferably be sufficient to cause a weight increase by swelling (absorption of the solvent) in the range of about 0.1 to 70 percent, and more preferably between about 0.1% and about 5%. Preferably the solvent is comprised of one or more compounds selected from the group consisting of aromatic hydrocarbons (including halogenated aromatic hydrocarbons) and halogenated aliphatic hydrocarbons. For example, a copolymer of 95% dicyclopentadiene and 5% ethylidene norbornene, when immersed for 5 minutes in toluene at room temperature, showed a weight gain swell of 2.9% and a fine uniform micro-etch of the surface. Immersion of the same polymer in 111-trichloroethane showed a swell of 4.9% after 5 minutes at 40° C. In the case of immersions in 1,2,4-trichlorobenzene and alpha,alpha, dichlorotoluene, swelling was 63.5% and 7.6%, respectively, and heavy microporosity was evident on the surface.
It is contemplated that with strong organic solvents, sufficient microporosity may be developed that the acid etching step may be eliminated prior to metal plating. The preferred organic pre-etch solvent will have a solubility parameter near that of the polymer. For the copolymer of 95% dicyclopentadiene and 5% ethylidene, a solubility parameter in the range of 9.3 to 11 (e.g., from 9.6 to 10) cal 0.5cm 1.5 was found to have the most swelling power.
A 4" by 4" by 0.15" thick specimen of RIM-molded Metton® LMR poly(dicyclopentadiene), molded with a cavity temperature of 90° C. and core temperature of 60° C., is immersed for 5 minutes in xylene held at room temperature (25° C.) as an organic pre-etch. This is followed by immersion for 5 minutes in a 70° C. aqueous etching bath containing 420 g/l of chromic acid and 325 g/l of sulfuric acid. The level of Cr3+ ion in the bath is about 7 oz./gallon. This is followed by sequential immersions in three rinsing baths of room temperature deionized water, then a neutralization step involving immersion for 5 minutes in a bath of 5% hydrochloric acid at room temperature, and then another rinsing in three sequential baths of room temperature deionized water. This is followed by immersion for 3 minutes at 40° C. in deionized water containing Condiriser SP at a concentration of 150 ml/l. Condiriser SP is a cationic wetting agent sold by Okuno Chemical Company, of Japan. It serves to place a negative charge on the surface of the etched part, which promotes the attraction of the positively charged palladium ions during the treatment with the chemical activator, described next.
Chemical activation of the etched part surface is accomplished by immersion for 5 minutes in a room temperature aqueous bath containing a palladium/tin hydrosol, Enplate Activator 850 (at a Pd/Sn concentration of 2%) and hydrochloric acid (at a concentration of 150 ml/l). This serves to deposit palladium ions on the etched surface. After several rinses in deionized water, the part is then immersed in a bath of dilute sulfuric acid at 40° C. for 8 minutes. The bath contains about 100 ml of sulfuric acid per liter of water. This treatment serves to remove excess hydrolyzed tin hydroxide from the deposits of palladium on the part surface, so that the tin hydroxide will not inhibit the deposition there of the plating metal, in the next step.
Finally, electroless deposition of nickel on the etched part surface is accomplished by immersion for 5 minutes in a nickel plating bath at 40° C. The bath, having a pH of 8.5, is a 20 volume percent solution of Enplate®n Ni-429 in deionized water. Enplate Ni-429, like Enplate Activator 850, is sold by Enthone-OMI. Enplate Ni-429 is an alkaline, electroless nickel solution.
Claims (2)
1. In a process of metal plating the surface of an object formed out of a cyclic olefin polymer, the improvement wherein the object is first immersed in an organic solvent that serves to swell the object at its surface.
2. The process of claim 1, wherein the polymer is a thermoset polymer of dicyclopentadiene, the organic solvent is one or more compounds selected from the group consisting of aromatic hydrocarbons and halogenated aliphatic hydrocarbons, the immersion is performed for a long enough time to cause the weight of the object to increase by about 0.1 to 5 percent, and the metal plating is performed in an electroless manner.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/113,331 USH1807H (en) | 1998-07-10 | 1998-07-10 | Organic pre-etch treatment for metal plating of cyclic olefin polymers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/113,331 USH1807H (en) | 1998-07-10 | 1998-07-10 | Organic pre-etch treatment for metal plating of cyclic olefin polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH1807H true USH1807H (en) | 1999-10-05 |
Family
ID=22348838
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/113,331 Abandoned USH1807H (en) | 1998-07-10 | 1998-07-10 | Organic pre-etch treatment for metal plating of cyclic olefin polymers |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH1807H (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030232214A1 (en) * | 2002-06-18 | 2003-12-18 | Veerasamy Vijayen S. | Method of making automotive trim with chromium inclusive coating thereon, and corresponding automotive trim product |
| WO2013083175A1 (en) * | 2011-12-05 | 2013-06-13 | Blue Wave Co S.A. | Construct comprising metalized dicyclopentadiene polymer and method for producing same |
| US20160303830A1 (en) * | 2013-12-20 | 2016-10-20 | Zeon Corporation | Resin material and resin film |
-
1998
- 1998-07-10 US US09/113,331 patent/USH1807H/en not_active Abandoned
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030232214A1 (en) * | 2002-06-18 | 2003-12-18 | Veerasamy Vijayen S. | Method of making automotive trim with chromium inclusive coating thereon, and corresponding automotive trim product |
| US6861105B2 (en) | 2002-06-18 | 2005-03-01 | Guardian Industries Corp. | Method of making automotive trim with chromium inclusive coating thereon, and corresponding automotive trim product |
| WO2013083175A1 (en) * | 2011-12-05 | 2013-06-13 | Blue Wave Co S.A. | Construct comprising metalized dicyclopentadiene polymer and method for producing same |
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