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Cherries & Cherish: brooches in metal and wood

I’m feeling a little panicked about the HSF, because I’m still behind on my #17 Robes & Robing challenge, and I have a big entry to the #18 Re-Make challenge still to enter (though I did enter two little items), and I’m behind on the 1860s elliptical hoopskirt I’m making for the #19 Wood, Metal, Bone challenge.

So, to mollify myself I whipped up two super simple little items that qualify for ‘Wood, Metal, Bone’:

Vintage & antique inspired brooches, thedreamstress.com

 

The first, in metal, is a portrait brooch inspired by 18th century portrait brooches and bracelets.

Vintage & antique inspired brooches, thedreamstress.com

 

I printed out Ramsay’s Portrait of a Lady on parchment paper and cropped the face to the right dimensions.  I really liked that she was an un-named woman, so that her face didn’t have any connotations other than sweet and appealing.

Lady, possibly of the Cholmeley family by Allan Ramsay, ca 1740 UK

Lady, possibly of the Cholmeley family by Allan Ramsay, ca 1740 UK

Then I lacquered the paper to finish and preserve it, and when it was dry, inserted it into an old brooch back with extra layers of cardstock to further protect it.

Vintage & antique inspired brooches, thedreamstress.com
The brooch looked to plain as it was, so I sewed faux pearls in a garland around the portrait.  Super simple, but rather effective.

I’d originally based the look of the brooch loosely on 18th century examples in paintings, but then I found this article from the Girls Own Paper:

Girls Own Paper, 1905-7, thedreamstress.com
I can imagine a girl in 1906 reproducing Ramsay’s painting rather than a portrait of someone she knew, so the brooch has become quite multi-period.

My second item is even more simple:

Vintage & antique inspired brooches, thedreamstress.com

 

Three round cherry-coloured beads, a bit of wool felt, a bit of embroidery floss, a brooch back and a bit of paste to stiffen my ‘stems’ and affix the brooch and I have a cherry brooch:

Vintage & antique inspired brooches, thedreamstress.com

 

I was originally inspired by craft how-tos in some of my 1930s magazines (a 1937 one in particular has a nearly identical how-to only with dangling flowers instead of cherries), but cherries were popular ornamentation throughout the 19th and early 20th century, so I could pin this into the trimmings of a Victorian bonnet without it looking too out of place.

Vintage & antique inspired brooches, thedreamstress.com

 

I have to say that while the cherry brooch is cute, and I’m still madly in love with the idea, I’m not entirely satisfied with the end result.  I want to keep working on it and perfecting it.

The Challenge:  #19: Wood, Metal, Bone

Fabric:  wool felt (cherry brooch).

Pattern:  None

Year: Portrait brooch:  mid-late 18th century/1900s;  Cherry brooch:  1930s

Notions:  Portrait brooch:  vintage  metal brooch back ($5), faux pearls, thread, lacquer, paper (stash); Cherry brooch: embroidery floss, glue, wooden beads (.90 cents).

How historically accurate is it? Portrait brooch:  More inspired than accurate, but the accuracy level improves if I consider it ca 1905 rather than 18th century.  Cherry brooch: other than the glue, my technique is nearly identical to a 1930s tutorial, so pretty accurate.

Hours to complete:  1.5 for the pair

First worn:  I’ll be sporting the cherry brooch on my jacket this evening

Total cost:  NZ$5.90 for the pair

 

Terminology: What are aniline dyes? (or, the history of mauve and mauveine)

Up until the mid-19th century, almost all dyes were made from materials found in plants (indigo, woad, woad, madder, brazilwood, tumeric and others), animals (shellfish purple, cochineal), and minerals.  While these dyes could produce an amazing range of colours, there were still some colours that couldn’t be produced by natural means, and some of the colours that could be produced by natural means were inclined to run, fade, or to destroy the very fabrics they dyed.

Then,  in 1856 William Henry Perkin, a young chemistry student, working at home, after hours, in a makeshift laboratory, trying to create a chemically identical artificial version of quinine (a very valuable plant-based drug which was used to treat malaria), thought to experiment with the results of another failed attempt.

The result of his experiment on his experiment was mauveine (also known as Perkin’s mauve, aniline purple, harmaline,Tyrian purple, plain old mauve, and, if you want to be extremely technical, 3-amino-2, ±9-dimethyl-5-phenyl-7-(p-tolylamino)phenazinium acetate).  Mauveine was  a combination of aniline (a common extract of coal tar) and other compounds which created a brilliant purple which was the first mass produced chemical dye.*  Mauveine would lead the way to dyes in dozens of other shades, all made from aniline from coal tar, and to everything from the modern dyes we use today, to cancer treatments.

Perkin called it first Tyrian purple, after the shellfish-based purple worn by Roman emperors, and then, when it was pointed out that this name was confusing (referring, as it did, to a real animal based dye), mauve, after the mallow flower.  In scientific papers he referred to it as mauveine.  I’ve chosen to use this last name, as it avoids confusion between mauve (Perkin’s colour) and mauve (the generic pinky lilac colour).

That’s the basic story of how aniline dyes were invented, but the backstory behind it, and the story of how Perkins’ initial experiment in the attic of his father’s house made him a rich man, are just as interesting.

To start with, the fact that Perkin was studying chemistry was pretty amazing in and of itself.  Chemistry was in its very infancy as a science, and most of the rest of the scientific and industrial world thought that chemistry, at best, produced a few neat party tricks but had little practical applications, and that at worst, it was just a new form of alchemy.  It is only because the English royal family had such strong ties with Germany, which had a chemistry community, that there was a school of chemistry at all in England for Perkin to study at, and a brilliant German chemist for him to study under.

Perkin’s discovery wasn’t actually unique: other chemists, and even Perkin himself, had noticed that extracts of coal tar could create colours.  As early as 1826 chemists had noticed that aniline was a component of plant based indigo dye.  By 1840 they knew it was also a by-product of coal tar, and that it could produce colours.  In Feb 1856 Perkin had even submitted a report on a bright crimson colour that was the result of an experiment with hydrogen and benzol (which is a byproduct of coal tar).  So Perkin’s great achievement is not that he found a colour out of aniline or another coal by-product, but that he pursued its possibilities.

Not only did Perkin pursue the possibilities of his discovery, but he did so in the face of great disapproval.  His father had not wanted him to become a chemist in the first place, and Hoffman, his brilliant German mentor, was not brilliant enough to realise that a chemist could be both a scientist and a businessman, and that practical chemistry need not detract from pure chemistry.  Hoffman called Perkin’s discovery ‘Purple sludge’ and told him that if he pursued industry, he would never be able to return to chemistry.

In order to make his colour into a dye, and his dye into a business, Perkin had to convince his father to bankroll what seemed a mad enterprise (too mad for any bank to agree to fund it) and leave his mentor, and (he thought) and chance of a proper scientific career behind.  Perkin risked everything, and he got his family to risk everything, for his idea.

The idea was pretty mad: Perkin knew that his solution dyed fabric a brilliant purple, but he knew nothing of the dye industry, nothing of fashion, and little of business.  To make matters worse, his initial mauve dye would not dye cotton: only silk and wool, and cotton was a hugely popular fabric in late 1850s.  Plus, extracted aniline was prohibitively expensive, making the production of the dye unprofitable.

Amazingly, Perkin persevered.  After much experimentation he found that tannin (the stuff that makes tea taste bitter if you let it sit too long) worked as a mordant which attached mauveine to cotton.  He figured out a way to extract aniline less expensively.  He also found a dyer to work with, found a spot for a factory, and built his own factory to produce mauveine dye.  That’s right – rather than discovering the dye and then immediately rolling in the riches, Perkins had to build his own factory to produce it, and find industry dyers to buy it.

Luckily for Perkin, his timing was perfect.  Just as he launched his first dyes, the French Empress Eugenie, the most fashionable woman in Europe, and certainly the most imitated in terms of dress, decided that lilacs, purples and mauves matched her eyes perfectly.  Probably on her advice Queen Victoria wore, to the wedding of her daughter the Princess Royal in 1858, a dress of “rich mauve velvet, trimmed with three rows of lace…the petticoat, mauve and silver moire antique”.  The mauve of Queen Victoria’s dress was more lilac than brilliant purple, and was almost certainly the product of natural dyes made from lichen, but the result was the same: all shades of purple were in.

Dress, 1862-1864, Musee McCord, M965.112.1.1-2

Dress, 1862-1864, Musee McCord, M965.112.1.1-2.  This dress could have been dyed with either natural dyes or aniline dyes – or both.

By 1859 an English newspaper wrote that Mr Perkin “can itinerate Regent Street and perambulate the Parks, seeing the colours of thy heart waving on ever fair head and fluttering round every cheek.”  The satire paper Punch, predictably, was less flattering and described London as being struck by an epidemic of mauve measles, a serious illness which began with “a rash of ribbons” and progressed to cover the whole body in mauve.  According to Punch women were particularly susceptible to the disease, but ‘a single dose of ridicule’ was usually enough to cure a man.

The popularity of mauve and mauveine dye was boosted by the fashion for the crinoline at its widest, and the increased lengths of fabric that took, not to mention the need for pretty stockings and petticoats that were often exposed by gusts of wind and unfortunate seating.

Fashion plate featuring a girls dress in mauveine, a ladies bonnet with magenta ribbons, and a walking dress in aniline green, English Woman's Domestic Magazine, June 1864

Fashion plate featuring a girls dress in mauveine, a ladies bonnet with magenta ribbons, and a walking dress in aniline green, English Woman’s Domestic Magazine, June 1864

Mauve, as exciting as it was, could not be the cutting edge of fashion forever, and in 1861 it was falling out of style, to be replaced by 1859’s  Verguin’s fuchsine (a rich crimson red, also known as solferino and magenta), and in the 1860s, Bismark brown,  Hofmann’s violet (a different vivid purple, and yes, its named after the Hofmann who derided ‘Purple sludge’),  Magdala red, Manchester brown, Martius yellow, Nicholson’s blue (a vivid teal blue), aniline yellow, bleu de Lyon, bleu de Paris, and aldehyde green.

To compete, Perkin came up with another flower-themed shade: dahlia, a colour between mauvine & magenta; the patriotic Britannia violet (appropriate as he was having to compete with numerous continental dye companies), which was a deep blue; Perkin’s green; an aniline black; and the rich purple seen in the frock below.

Day dress, Great Britain, United Kingdom, France, 1873, Silk and ruching, Victoria & Albert Museum T.51&A-1922

Day dress, Great Britain, United Kingdom, France, 1873, Silk and ruching, Victoria & Albert Museum T.51&A-1922

While the best known and most obvious aniline shades are extremely bright and vivid, not all aniline dyes are extremely bright.  Customers enjoyed the novelty of bright shades which had never been previously possible, but aniline dyes were also valued for their washability and lightfastness.  Dyers such as Perkin went to great lengths to prove that their dyes were more durable and washable than natural dyes, and that the only aniline dyes that faded, stained and came out in the was were those that were prepared and dyed improperly.  Part of what made aniline dyes so successful is that they had attributes that made them valuable beyond their initial aesthetic: they were easier to source, cheaper, and often worked better than their natural alternatives.  From the very early years of aniline dyes, muted, subdued aniline shades were made and sold, but it is much more difficult to identify garments made from aniline dyes in shades that could also be made from natural dyes.

All the new aniline dyes became more and more popular, the market for natural dyes collapsed.  Cochineal dropped in price from 15 cents per kilo in 1858 to 8 francs in 1862, safflower from 45 to 25 cents per kilo.  The madder industry was wiped out forever.  Even when the fad for the brightest, most vivid, early shades disappeared, the old natural colours were replaced by synthetic variants.  Aniline dyes were here to stay.

Dress, Paris, France, 1869-1870, Vignon, Ribbed silk trimmed with satin, faced with cotton, brass, Victoria & Albert Museum, T.118 to D-1979

This dress may have been dyed with ‘dahlia’ or a similar shade, or even a natural dye. Paris, France, 1869-1870, Vignon, Ribbed silk trimmed with satin, faced with cotton, brass, Victoria & Albert Museum, T.118 to D-1979

And what of Perkin?  I’m happy to report that he reaped the benefits of his discovery, his daring, and his perseverance.  His business prospered, he became comfortably wealthy, respected as a businessman and a chemist.  He continued to make important scientific discoveries throughout his life  Tragically, he lost his first wife to TB, but he had a happy second marriage, and his children went into the family industry.  Ironically, it was the scoffing Hofmann who initially was given (and happily took) the credit for the discovery of aniline dyes, but Perkins preferred research, work and family life to an endless round of speaking and adulation.  As the 19th century passed his public profile rose and rose, until the 50th anniversary of his discovery was commemorated with dinners and medals across the globe.

* Contrary to popular belief, mauveine wasn’t the first chemical dye.  In 1771 indigo was combined with nitric acid to dye silk a bright yellow, and both red aurin made from carbolic acid and deep blue pittacal made from beechwood tar were discovered in 1834.  The difference is that none of these was produced in any notable quantity, nor did they inspire chemists and dyers to pursue other chemical based dyes.

For more examples of aniline dyes, see my pinterest page.

Sources:

Finlay, Victoria.  Colour: Travels through the Paintbox.  London: Hodder and Stoughton.  2002

Garfield, Simon.  Mauve: How One Man Invented a Colour that Changed the World.  London: Faber and Faber Limited.  2000

Rate the Dress: 1860s paisley & swiss waists

There were a whole range of ratings on last week’s quite embellished stripey ca. 1880s frock, from “Want it now!” to “Ewwww….armpit ruffles.”  I’m very much in the LOVE.MUST.RECREATE.NOW camp, but I think if I did recreate it, I’d end up tweaking a lot of things just a tiny bit, so I can understand the final rating of 7.3 out of 10.

I don’t know what the logic of this week’s dress is in relation to last week’s frock, except that I woke up today and thought “I’ll post that dress”.

So here it is:

Early 1860s.  Coral-y orange-y pink.  Paisley, ruffles, a swiss waist bodice, but all quite restrained.

It has some slight display issues in the back, with an odd skirt fastening, and a poor replacement lace, but I’m sure you can overlook that and focus on the dress as it was meant to be worn.

What do you think?  It’s a dress that could be either too simple, or too frilly, depending on how you look at it.  The colour is a tricky one.  The swiss bodice is a bit unusual.  In fact, in a strange way, it could garner all the same criticisms that were leveled against last week’s dress.

Interesting…

How will it fare in comparison?

Rate the Dress on a Scale of 1 to 10.