In June 1929, Berchet began work at DuPont.[6] Berchet was a member of a research group led by Wallace Carothers actively working on polymerization in "Purity Hall" at the DuPont Experimental Station. Some others working in the group were Paul J. Flory, Charles Stine, and Julian W. Hill.[7]
The assignment of the group was to make polyesters via condensation polymerizations. Their initial attempts to create suitable commercial fibers failed as the fibers, while uniform and appearing to be strong, elastic and resilient, melted at low temperatures and were soluble in solvents. The group then turned their attention to using diacidic and dibasic molecules to create polyamide fibers based on condensation reactions.[8]
During his time at DuPont Berchet played a pivotal role in the invention of neoprene and nylon. However, he is fully credited with neither discovery. In March 1930, Berchet was the first to synthesize neoprene by combining monovinyl acetylene with concentrated hydrochloric acid, but Arthur Collins was the first to discover neoprene several weeks later on April 17, 1930, since Berchet did not examine his sample until late April.[4][9] Under the direction of Wallace Carothers Berchet synthesized nylon 6-6 from equal parts hexamethylenediamine and adipic acid on February 28, 1935.[3][10]
Berchet served in the patent section at DuPont rather than the chemical department in the years following World War II.[11]
Wallace Carothers assigned Berchet to isolate vinylacetylene in early 1930 as part of a larger project on divinyl acetylene. Fr Julius Arthur Nieuwland, a professor of chemistry at the University of Notre Dame, had produced divinyl acetylene during his research on acetylene chemistry. DuPont purchased the patent rights for divinyl acetylene after Elmer K. Bolton attended a lecture by Nieuwland.[12] By February 20, 1930, Berchet had isolated enough vinylacetylene from divinyl acetylene to study. After a series of inconclusive experiments, Berchet, under the direction of Carothers, treated monovinyl acetylene with a variety of reagents and put 25 samples in sealed containers.[9] One of these samples was monovinyl acetylene combined with concentrated hydrochloric acid. However, Berchet let his samples stand for five weeks on his laboratory bench before determining what transformations might have occurred. Before Berchet examined his samples, Arthur Collins accidentally discovered chloroprene on April 17, 1930, by combining monovinyl acetylene with concentrated hydrochloric acid. Arthur Collins was assigned to Carother's group in early February and had previously worked with divinyl acetylene while at the Jackson Laboratory.[4] Chloroprene, now known as neoprene, was the first synthetic rubber. DuPont marketed the product under the name DuPrene in 1931.
Carothers' group at the DuPont Experimental Station had been using condensation polymerizations to make polyester, but the fibers melted at low temperatures and were soluble in common solvents and were therefore not suitable as commercial products. Carothers' group turned their attention to using diacidic and dibasic molecules to create polyamide fibers.[13]
After several failures, the group completed a systematic study of potential polyamides by combining diamines with a similar series of diacids.[12][10] 81 potential candidates for polyamides were identified, and in 1935 Berchet was assigned to the polyamide project to work on them. He constructed and purified many of the diamines so they could be polymerized. In his research Berchet made examples of several other types of polyamide polymers.[10]
On February 28, 1935, Berchet prepared nylon 6-6, a condensation copolymer constructed from equal parts adipic acid and hexamethylenediamine.
Berchet's laboratory notes from his creation of nylon 6-6 are as follows:[14]
Adipate of hexamethylene diamine
7 g. diamine, 8.8 g. acid and 20 cc. m-cresol heated 215° for 3 hours. Water came off during the first half hour. The temp. was then raised to 255-60° and the cresol distilled off in the vacuum. The residue solidified at one time but then melted again at 265°. It was heated under 1 mm at 265° for 3 hours. On cooling (overnight) the polymer broke the flask by contracting and showed a tenacious adherence to glass.
It was a very hard, horny solid melting at 252-254°. It was very readily spinnable. Sample turned over to D. D. Coffman.
There was obtained 12.5 g. of polymer, yield 90%.
3/1/35 GJB 3/21/35 H. B. Dykstra
The half-ounce of pearly, lustrous mass obtained became DuPont's nylon. The fibers formed were elastic and strong after cold drawing and were both unaffected by water or most solvents and had a higher melting point than previous fibers.
The fibers were initially called Fiber 6-6, but were eventually named Nylon 6-6.[10]