Science topic

Silk - Science topic

A continuous protein fiber consisting primarily of FIBROINS. It is synthesized by a variety of INSECTS and ARACHNIDS.
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I am working on silk nanofiber for preparation of wound healing patches
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it is possible to dissolve up to 20% (w/v) silk fibroin in Ajisawa's reagent, although the optimal concentration may vary depending on the specific application.
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Here's an example, Francois Quesnay's economic table. As a doctor, Quesnay sees the
economy as a huge organism, and the precious economic surplus is like a blood supply function
vital to life. To explain this view, he made the first economic "model" (model), a simplified economic map. Quesnay created it in his original book, The Economic Table (Economic chart). He outlined many curves to represent the resources circulating around the economy. The peasants produced the economic surplus and paid the rent to the nobles who owned the land, who then bought the silk buttons and the silver candlesticks from the hand craftsmen. The craftsmen in turn bought food from the farmers to complete a cycle. The economy is a kind of surplus circulation formed between the peasants, the landlords and the hand craftsmen.
This economic table can be written as the following program diagram:
Farmers' production and economic surplus→Pay the rent to the nobles who own the land→The nobles then bought silk buttons and silver candlesticks from the handcraftsmen→The craftsmen in turn bought food from the farmers.
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From the viewpoint of scientific methodology, human economic activity (action) can methodically be described as a program as your Duan Xian Xiang simple flow diagram of Quesnay implies.
As human economic activity is driven by preferences and priorities, under the condition of finite choices in lifetime, the identification of values plays a key role as well as the availability of resources.
A very important aspect in modern mass media societies is the psychological factor of marketing ideas, values and products, which are no more driven by basic life needs, but by to https://dictionary.cambridge.org/dictionary/english/keep-up-with-the-joneses.
Consequently, accumulated human economic activity has a lasting impact on the physical environment, in terms of sustainability.
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We are trying to make Silk fibroin and PVA blend solution in formic acid for electrospinning but it is not miscible. I tried following
1. I tried to dissolve both in 99% formic acid but the solution wasn't look proper for electrospinning.
2. I also tried to mix the both by dissolving individual in formic acid.
3. I also tried to mix by dissolving silk in formic acid and PVA in water.
In all three cased i didn't get the homogeneous solution for electrospinning
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Kindly follow the reported work
I hope it will help you.
Thanks and Regards
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Dear members of the community,
I am trying to elaborate silk fibroin. I boiled the silk for 30 min. Then, when it is dry, I cut it in small pieces and dissolved it with 9.3 M Libr solution (I put 5 mL of solution for every 1 g of silk fibroin).
Then it put it at 60 º for 4 h and at that point I manege to dissolve the silk. Sometimes I have to gently stir with a spatula since otherwise there are some parts of silk on the surface that will not dissolve . After the 4 h I obtain an amber solution with black beats and also bubbles. Also, it seems like there is not 100 % solution, it looks like some parts are a bit gel. Is it normal?
Then, I put this solution into a membrane to dialysis at 4 º but it gels during the process. I put the string bar at the lowest and I change water after 1 h 4 h 6 h and then every 12 h. The whole process takes 48 h. When I add the water it is at room temperature shall I cool it to 4 º before conducting the change?
I read several solutions like boiling the silk for 45 min, adding more LiBr solution or one more concentrated, increase the oven temperature to 80 º. What solution would be the best? Am I missing something?
Thank you in advance for your help,
Enric
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I have an experience with the same issue, but you must take care of the PH, which is an important parameter.
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Dear colleagues,
I want to simulate the maize grain number with 6 level temperature stress experiments by APSIM-MAIZE. I have tried to modify the temperature fuciton from the default value (8, 34, 44℃) to a modified value (5, 30, 41℃), which concluded from Wang (2018).But, the simulation was not good for grain number.
Thus,
(1) how to modify the temperature function with my heat stress experiments?
(2) what's the calculation formula for maize grain number in the Maize Module?
in addition, my phytotron controlled-temperature experiment were conducted with 6 temperature from 30 to 40℃ during maize silking period.
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Hi, everyone my name is Tesfalem, MsC student at Warsaw university of technology. I wanted to do a research on maize grain storage which can be used to store for extended period of time without deterioration. Before selecting materials and do simulation of the storage I want you guys to tell me about how to model and simulate temperature distribution of the maize grain with in 1 m diameter circling.
Thank you.
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I have been encountering challenges in my Nematology work especially when using Galleria mellonella (Greater Wax moth) as a bait to Entomopathogenic Nematodes. The larvae will produce silk that helps it to enter the pupal stage without getting infested by Entomopathogenic nematodes in the soil sample. How do we control the silking to enable easy penetration and subsequent infestation by Entomopathogenic Nematodes?
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I can recommend a heat shock to block the spinning of the cocoon. Briefly, you prepare hot water (56 °C) and pour it on the larvae for 15 s. The detailed description can be found here: https://orgprints.org/id/eprint/11200/ .
Good luck with the isolation of EPNs!
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How should the maximum temperature be measured for new composite materials made of silk and epoxy?
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did you mean the max temp. of new material or the temperature that the composite should work w/o failure?
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New composite materials from silk and epoxy material
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See also the following very good link: https://www.nature.com/articles/s41598-017-11919-1
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What number of days to 50% silking can be used to predict the maturity of maize? for example early maturing verities may have a range 56-63 days to 50% silking.
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In our case, just you double the number of days to 50% silking that will be the tentative days to physiological maturity. For example, if days to 50% silking of a variety is 60, then the days to physiological maturity will be 120 days.
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I am running a degradation study on dissolving silk in a formic acid calcium chloride system and I was wondering why the solution turns from clear to a darker purple/black that darkens over the course of a week. Does anyone have any ideas on what chemical reaction is occurring that is causing the solution to turn purple? I've included images of my solutions, the first solution was degrading for about 30 minutes and the second for a couple weeks.
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Dear Kyle Printon
I’m not sure but depends on your attached photo, this may be due to the presence of copper impurities lads to the formation of Copper formate that reacts with ammonia released from amino acids degradation of Silk and formed copper ammonium salts or copper ammonium formate complex.
good luck
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I'm working on an aquatic insect that produces silk and I would like to know if every silk has a composition of fibroin (highest percentage) and sericin. Thank you!
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Thank you!
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I'm following the instructions here to create a 3D printable bioink but after i freeze dry my samples, they only partially dissolve in water. I tried heating with a stir bar too and it would still not completely dissolve. In the paper, they describe their Sil-MA composite as a powder after freeze drying but my sample is more similar to a strong Styrofoam. I cannot grind it up with a mortar and pestle and cutting it is very difficult. I've had relative success dissolving it in formic acid but but i think the acidic environment hinders crosslinking so I'd perfer to use water as the solvent instead. Any ideas?
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Dear Kyle Printon, I think freeze drying has introduced denaturation of silk. My Regards
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The data is attached below. Please give me technical advice!!
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Wondimagegne A Mo Deconvolution of a composite peak into its individual peaks plays an important role in the interpretation of many types of graphs including XRD, XPS, FTIR, and PL etc. In this video, I have discussed how to deconvolute simple combined peaks, composite peaks and how to correct missing data in a given peak with the help of deconvolution. In the case you want to further ask about it, please do comment on the specific video, I'll respond to it shortly. I have provided the practice filee (OriginLab) here. Thanks
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Hello,
I'm working on the flowering of maize, and more particularly on ASI. This year i would like (for my job) to make a selection in the objective to reduce ASI. But I didn't find any informations about how to do in litterature. Could you help me please?
Thank you very much
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Dear Jean Mergnat I am attaching two relevant pdfs; hope, these may be useful to you.
My best wishes, AKC
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We are looking for edible fibers that can be used in the food industry
does silk fiber edible? And does the FDA approve?
Many thanks for considering my request.
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FDA has specific requirements for certain dietary fiber claims. A product must contain 20 percent or more of the DRV per reference amount customarily consumed (RACC) to be considered “high” in fiber and between 10 and 19 percent to make a “good source of fiber” claim
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In most cultures, traditional textiles use natural dyes, unbleached materials and white cotton/ linen/silk which is beautifully synchronized with the concept of sustainable living. In today's fast-fashion scenario, how many people prefer/use undyed materials.
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Percentage-wise less than 5% of consumers prefer undyed textile fabric for apparel.
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I have some question about the laboratory process of extraction silk fibroin from Bombyx mori base the Prof. Kaplan protocol. How much Silk cocoon need for 20 experiments? How dialyzes the final product? How long can I keep Silk ّFibroin? Thank you for your responses in advance.
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hi, it's better to use cassettes with MWCO of 3500. also as fibroin is a high molecular weight protein and does not pass the cassette you can use cassettes with up to 14k MWCO.
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Hi all - a puzzler for you. We're using the protocol detailed at https://www.nature.com/articles/nprot.2011.379 to extract and isolate silk fibroin from silkworm cocoons. In brief, you boil 5 g of cocoons in 0.02 M NaCO3, wash the matted silk fibers in H2O, and then dissolve in 9.3 M LiBr.
Some people in our lab find that after dissolution in LiBr, they get a pale gold solution (roughly the color of a lager). But some people get a rose gold/pink solution. If you move on to the dialysis steps later, you eventually see the pink fade to the normal pale gold. Anecdotal evidence suggests that if you do a better job washing, you are more likely to get the pink, and pink solutions tend to be slightly more acidic.
Any ideas why this is happening? In my naive understanding, colors tend to mean pi bonds...there are a large number of tyrosine residues in silk (288/5,525), some tryptophans (13/5,525), and some phenylalanine (37/5,525). Silk is also especially prone to assembling into beta sheets--though the point of dissolution is supposed to be disrupting those.
Possibly also relevant: these solutions are normally made in house DI water, not 18 MOhm water.
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In our laboratory we've found that the pink/gold phenomenon depends on our LiBr source/batch, although I would guess that you're using the same LiBr :/
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Is there any simple chemical analysis method, by which the removal of outer sericin protein layer from raw silk fibers (after de-gumming) can be confirmed?
There are techniques likes weight loss, FTIR, FE-SEM, XRD, SAXS, Contact Angle, DSC, & TGA, for the confirmation (I have tried these techniques).
But, I want to know about any simple chemical analysis method, which can help in confirming the removal of sericin protein layer from de-gummed silk.
Thank you.
Kind regards,
Prakash
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The quite universal method is to check the weight loss (should be between 25 and 30%), then image analysis can help (SEM). Spectroscopic methods would be inefficient because both fibroin and sericin are proteins and they are difficult to separate in FTIR.
GPC could be a nice idea, cause the the two molecular weight are quite different.
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During inspection of #maiz found one plant grown as lower half part of #tassel and upper half part as #silk at terminal region. This is the first time I have seen...It looks amazing to me.
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I have seen similar symptoms in maize but only where there were several plants with similar symptoms. We put it down to herbicide damage but cannot be sure; was it sprayed wit a herbicide?
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I need to know the heat and moisture production of any silkworm larvae period for supplementary heat.
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Here is a useful article for your query.
Management of Climatic Factors for Successful Silkworm (Bombyx mori L.) Crop and Higher Silk Production: A Review
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I am doing Immunocytochemistry (ICC) to detect vinculin on hWJ-MSC which seeded on silk scaffold. I want to know perfect time to fixate the cell (start the ICC protocol) so that i can observe vinculin on fluorescence microscope.
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24-48h
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The Belt and Road Initiative (BRI), also known as the One Belt One Road (OBOR) or the Silk Road Economic Belt and the 21st-century Maritime Silk Road, is a development strategy adopted by the Chinese government involving infrastructure development and investments in 152 countries and international organizations in Europe, Asia, Middle East, Latin America and Africa.
The BRI is twelve times more than the Marshal Plan. Do you believe this initiative will change the world? Is your country joining this initiative? Why do you think the BRI is good or bad for your country?
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It depends on how you define the word "change". If you are referring to the life condition of people in certain areas, then probably this program will do. But if you mean Chinese government will be the new leader of the world, then definitely NO. China is by far unable to produce any cultural hegemony to confirm its status as a world leader. Look at Chinese people themselves. Aren't they trying hard to learn English so that one day they can go to study or even live in the USA?
If China cannot come up with its own system of cultural hegemony which is made up of a series of dominant discourses, BRI will be money down the drain. But it is still a good attemp to challenge USA, making it more aware of what it is to the world.
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Hello,
I have to build up a new calcium imaging system which has 340nm and 380nm LED´s (should be very new on the market). When I load my cells (e.g. mouse neurons from DRG´s or recombinant cells) with Fura2 (3µM for 45 min. incubation) I get nearly no signal. What I noticed is, that my baseline starts at a very low ratio (~0.05). I have rowdatas of 500 at 340nm wavelength, and 8000 at 380nm. Normally the baseline is between 0.6-0.9, isn´t it? I also have an older Setup with an arc lamp. There I normally have rowdatas of 150 at 340nm and 200 at 380nm. Could it be that my intensity of the 340nm is too low? Or is the 380 nm too strong?
Does someone knows what my problem can be? I´m grateful for any idea!
Thank you!
Silke
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Hi Silke,
From your description I find it unlikely that the problem is in your optical system, since the raw values from your LED are many many times higher than that of your arc lamp (unless there was a change in the camera exposure, but I will assume there wasn't).
One issue of using LEDs for ratiometric assays is that there is no guarantee that your different LEDs will have the same output power. There is a chance that your 380nm LED is simply a lot stronger than your 340nm, since it is a significantly longer wavelength (so that you will have a lot more photons for the same output power with your 380nm). It might be interesting to check the output power and calculate the luminace of each LED to see if your raw values make sense.
Alternatively, you might consider switching over to a non-ratiometric method. I don't really know for synthetic dyes, but for genetically encoded calcium indicators, such as GCaMP, non-ratiometric measurement is pretty much the standard. You would need to change your LEDs to match another wavelength, but it might be worth a shot.
Hope this helps and good luck!
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How to get rid of the insect from the pupae (Silkworm) because the silk yarn is very strong and need any parts of the mouth and not the absorbent pipette as the butterflies?
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You can kill the adults inside the cocoons by baking them in a hot oven.  Then you can soak the cocoons in boiling water to loosen the threads.  You need to find the end of the thread and place it on a winding bobbin.  Then a machine unrolls the cocoon, winding the silk from five cocoons together to make one silk thread.   Then the thread is woven into cloth. 
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China's economic and technological growth has made it a global power with geopolitical impact across Eurasia. The country borders on 14 states and has a direct maritime border with three others (Japan, Philippines, South Korea and Taiwan - not recognized as an independent state).
In this sense, the Belt and Road Initiative is not only a plan for building infrastructure but a broad vision for the future of Eurasia integration. This strategic vision comprises geo-economic elements and is based on geopolitical factors. The ability to move forward with the values and ideals that surround the initiative will be essential for its consolidation.
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The Silk Road connecting China with the rest of the world. It is considered the most important commercial road that was used by Muslims to spread the Islamic Religion to countries in Asia. Also it was used to exchange goods between China and countries in Asia, Africa and Europe.
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I have used 9.3M LiBr solution to dissovle silk fibroin according to nature protocol at 60oC, and the ratio is 1g:4ml. But silk is not soluble completely so i can't use the solution. Can you give some ideas or where was i wrong?
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Try to increase temperature to 70 degree celsius or increase the boiling time to 1 hour twice during degumming.
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I have been following your researches, because they cover partly my area of scientific research interest? The international trade was mainly reorganized during and after the second World War, although ancient times and afterwards long colonial history shaped trade paths that remained as a heritage of the trade roads.
Since 2015 I have been deeply analysing the Belt and Silk Road Initiative and the AIIB establishment (already in 2015 as a competitive solution to TPP Trade Deal of the US and 11 other Pacific Rim nations). Unfortunately TPP was abandoned by US and is being revamped, now. (The TPP part is not my strength)
More important from my point of research is to find out the key expansion goals of China or rather empirically verify my thesis about long term process of internationalization, which in my perception is the final stage of China's attendance in globalization - mean World supremacy.
I am not judging positive and negative aspects of that process, at least at this stage, but I am trying to verify macroeconomic drivers of such decisions, apart from political once. In my opinion the New Silk Road project, supported by various financial means (solely Chinese or more complex international), due to its scale is comparable with the Marshall Plan that created Western countries' economies after the Second World War and which set economic global connection, existing till present times.
The second part of my scientific research is focused more towards the AIIB itself and perspectives of its role, towards internationalisation of RMB, at least in investment settlements and then in trade once. The ultimate question is whether China wants to internationalize RMB and if yes whether its economy is ready for that. This question is important in relation to the establishment of clearing offices around the World and relatively tiny share of RMB in trade deals clearance. Most of them is cleared in USD.
Bearing the above in mind I would like to ask you the following questions:
1. What are the main goals of your project: "International trade"?
2. Are you planning to utilize gravity model?
3. What scope will it have? Asia-Pacific Rim?
4. Are you in the process of setting up a team? I would like to participate.
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I wonder why Karol Piekarz does not reply himself.
Thank you for your comment. I know that you have freedom to readjust the "distance" between countries to a more "sophisticated" measure. I posed that question only to express most simple problem of the model. However, the gravity model has many other deficiencies as a trade model.
When I wrote that gravity model "is a very coarse one", I was saying that gravity model uses the same "distance" are all common for any industry, but as you can easily see that the ratio of trade and transport costs differs enormously and it would be difficult to characterize competitiveness of a product of a nation simply by distance.
Now, we have much more refined theory than gravity model. Please see Section 9 of my paper:
The new theory of international values is a model of international trade for M-county, N-product economy with choice of production techniques. It is also a unique theorem that can treat input trade (trade of input goods) which is now the vital or essential elements of international trade. For example, a global value chain is a network of input trade. Four generations of trade theory (Ricardian, HOS, New and New New trade theories) cannot deal with input trade. The first three theories simply exclude input trade (or intermediate goods) by assumption, whereas the fourth is a theory of a nation that trade with the world and does not analyze a simple situation that exported parts or components from country A to B changes the cost of a product in B and became competitive to the same product produce in A.
Gravity model is only accepted as relevant model of international trade after the failure of Heckscher-Ohlin-Vanek models revealed to be a complete failure in 1990’s. It is often explained that Eaton and Kortum model presents a theory why the gravity model is justified. On this point, please see my question and discussion there:
https://www.researchgate.net/post/Why_did_Eaton_and_Kortum_model_perform_so_badly )p.push(n[j]);p.length>1&&p.sort(function(a,b){var c=0;retu
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Nagano sensei, how can I help you with your Silk article?
AJ Jacobs
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Help can be done with each other which create good friendship.
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For a study I need to solve silk cocoons...
after degumming them in boiling NaHCo3 for 1 hour, we used the trinary solvent (CaCl2, H2O,C2H5OH ) during 4 hours and heated to 60 c ...silk cocoons didn't solve completly....how much does it take to dissolve them compeletly!the changes after 4 hours are so negligible....!what should I do?Have we ignored sth?
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Here I mentioned only Glass rod and silk cloth. This can be anything from triboelectric series. But, why should it happen? Why should different charges accumulate in two materials and then neutralized again when coming into contact? Why can't the charges gaining energy when rubbed get distributed in the same material itself? And, how this phenomenon happens in insulators?
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I wanted to known how much percent of silk protein is forming particle in the system.
eg. If I add 5% of silk protein in acetone then how will find how much particle is formed .
And how would I able to separate unreacted one.
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After centrifugation disperse your colloidal nanoparticles in acetone or ethanol and again centrifuge it. You will get pure nanoparticles
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Can anyone suggest me a cheap source of silk cocoons in Pakistan? I need to extract silk fibroin from it.
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You can check
Glorex International
Buyer From Karachi, Sindh, Pakistan
Yarn silkworm cocoon
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While preparing Silk solution from degummed silk fibroin by the LiBr method, I am finding that my solution is solidifying in the dialysis step or upon storage at 4 degree. In case it is not solidifying, white thread like materials are emerging which cannot be removed upon centrifugation at 1100 rpm for 20 mins.
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It is turning gel like. Not sure if it is sedimentation or solidification. On centrifuging, the solid gel is settling leaving clear water on top.
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We've just found an amount of silk without any notification of whether it is just silk fibroin or fibroin+sericin combination. Although it looks like cotton wool, we wanna be sure that it doesn't contain sericin.
thanks in advance
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Thanks a lot for the answers!
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I have observed two silk work cocoons (which look like tasar silk worm cocoons) on an eucalyptus tree in my clonal trial at Navsari, Gujarat. The cocoons were collected from 12 m height. Has anybody observed such cocoons on eucalyptus? Is there any earlier reports?
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Really good to keep the discussion going on.
May be to confirm the host nature of eucalyptus_you can tear tasar silkworms. Try to make an attempt.
Keep me updated. Really interesting observation
Good day
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I obtained silk from bombyx moori after lithium bromide treatment. The aqueous solution I get solidifies when I try to mix the drug in it using magnetic stirrer which is very difficult to use for electrospinning. How can I get rid of the problem?
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Dear Muhammad Samie
How much quantity of Drug you are adding with the silk solution?.
Try this method:
1. Buy silk cocoon and dewax it.
2. Use THF as solvent and mix the drug and silk with it.
3. You are now ready to spin.
All the Best.
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I have been using PBL for two decades now. Two things struck me in the goups randomly assigned to work together. I wrote about this extensively in the endnotes section in my book on TE Education since it is something of a hobby horse of mine. The process of using this teaching strategy, even in large groups, is explained fully ther
The group might be dysfunctional for various reasons but usually the two reasons I gave above in the question predominate though I tried to minmise them by randomly assigning group leaders for each group.
I also encountered both problems mentione above during my elearning course, and frankly found the ostracising one much more disturbing personally.
I never liked giving group assignments as an assessment strategy; the PBL presentations were a simple teaching strategy to engage students with learning and further reading as required at HE level.
Once I was constrained by student demands to give them the option of doing an assignment in pairs. If done in pairs both students had to write a small reflection on the whole process. Reading the reflections, everything was as smooth as silk, which made me sceptical of course.
Come a year later I learnt how the assignment was done by one person while the other did the assignment of the other study unit in a couple of instances; so much for the reflective account..
With regards to group assignments allocated by other academics, I had heard too much hoary incidents by students confiding me, to even remotely consider it, hence my duo students effort.
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Journal wise, it's a bit like an annotated bibliography, in which they keep their research and record thoughts and reflections, more context orientated than the reflective journal which I suppose in this case is more concerned with content and form.
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We use Galleria melonella for toxidity-tests in our lab. I am breeding them by myself, but it's disturbing, that they always producing silk and spin a cocoon. (If you buy them in a pet-shop, they don"t). So does anybody have an idea, how to stop G. melonella from producing silk?
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Well, I am afraid that you can not prevent them from producing silk. These are greater wax moths and they will produce the silk cocoons. It is one of their invasive tactics to infect honey bees in wild. If you can prevent them from producing silk, they will never be able to damage any honey combs.
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Silk waste can be felted. Can the waste from bamboo silk also be felted?
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The surafce of silk fiber is very smooth and therefore unlike wool, silk cannot be felted. You can modify the surafce of fiber by depostion tor by laser itching and then can try to carry out felting.
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My question is how I can protect myself and my colleagues against the toxins Thaumatopein, because I get very large allergic reactions on my skin?
Could someone tell me, can I do insolation od silk fiber on other way?
I'm posting the nest of Thaumetopoea pityocampa Schiff .
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Dear Rudolf,
I'm working on project with there fibers and I have contact with animals only while taking fiber from nests. I will try with protective colthing with membrane.
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I'm currently working on my Supply chain management dissertation and I need some research question on the New silk road's logistical and transportation process.
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Hi,
Primarily with the land base and marine base silk routes will have two significant features. Land base: lead time will be reduced by half & but the economics of scale will have an impact.
Marine route: Lead time high, economies of scale wise worth, 
Even you could see the greenness differences and what type of products which are appropriate for land base route and vice-versa.
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Silk fibroin is a well-known biodegradable material, and there are hundreds of publications about the usage of silk fibroin in tissue engineering, wound healing, drug delivery etc. However, silk sutures are non-absorbable (non-degradable), as indicated in the suture selection guides of all the suture manufacturers.
So... is silk fibroin degradable or not? If it is degradable, why is it used for the non-degradable sutures?
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The major component of silk is Fibroin Protein which mainly consists of repeated units of amino acids........Gly-Ser-Gly-Ala-Gly-Ala......it makes a beta-pleated sheet. The presence of high proportion of Gly makes a possibly more tightly packed structure which remains stable against even some acids and bases. However, the slow degradation process has been reported by many investigators.
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I'm on a low budget, which is why i opted for urea because it is supposed to reduce the hydrophobicity of the fibroin protein, but so far I've achieved nothing with it.I In my last attempt, I dipped the two cocoon silks in 9.3 M of urea for 4 hours at a temperature of 60 degrees celsius. Any suggestions? Thanks in advance. 
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Hi,
Its an interesting question that I like to discuss it further: before, I like to ask
Could you find a way to dissolve in urea? or not yet?
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I need spectral transmission characteristics of textiles (materials for clothes) in spectral range (380-1500) nm, and a little less for UV. Especially I need transmission characteristics for: tosilk, cotton, wool, linen, hemp fiber, viscose fiber, bamboo, acrylic, nylon, polyester, polyamide, elastane.
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Labsphere propose this kind of apparatus
Best regards
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I am going to extract silk fibroin and make scaffold (HFIP sponges) of it. Now in the article that I am following, u need to lyophilze the silk solution through freeze dry method but I don't have freeze dry facilty so can I use vacuum lyophilization instead. Your valuable suggestions will be highly appreciated please.
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Dear all, there is some confusion in the expressions used:
Lyophilisation = originates in the French language ( = freeze drying (US term)) and means sublimation drying (in vacuum; directly from solid to vapour) followed by conventionally (convective) drying of non frozen water (due to strong bonding of the watermolecules to solids)
Vacuum lyophilisation = vacuum freeze drying (this is the standard) as opposed to atmospheric freeze drying (this is what the South Americans did in dry and cold climate with a lot of solar radiation)
Vacuum drying = is low pressure (therefore lower boiling temperature of liquids) drying of unfrozen material.
Foaming may occur during early stages of freeze drying or vacuum drying, esp. if you have highly concentrated sugar solutions (grucose, fructose, lactose...)
Yours,
Harald
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The chinese government released a test guideline namely, "Test guidelines on environmental safety assessment for chemical pesticides—Part 11: Silkworm acute toxicity test"
The guideline I got from Internet is in Chinese language. If anybody having the English version of the guideline, please share with me.
Thanks  
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Dear I hope this be helpful for you
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China Announced 21 Test Guidelines on Environmental Safety Assessment for Chemical Pesticides
Original Article from CIRS
On 10 October 2014, the Administration of Quality Supervision, Inspection & Quarantine(AQSIQ)and the Standardization Administration of China(SAC)jointly held a press conference in Beijing, announcing the approval and release of the Test Guidelines on Environmental Safety Assessment for Chemical Pesticides (the Guidelines for short in the following contents) and other 32 key national standards. Institutes that are responsible for setting the Guidelines and other 3 standards attended the conference and introduced the background, contents, application, targets and significance of these documents to the media.
The Guidelines (Standard Number: GB/T 31270.1-2014 -- GB/T 31270.21-2014) was formulated by The Institute for the Control of Agrochemicals under the Ministry of Agriculture (ICAMA) in cooperation with Nanjing Institute of Environmental Sciences of the Ministry of Environmental Protection and other 11 research and education institutions. The Guidelines will provide very important technical specifications for environmental test of pesticide registration.
Consisting of 21 parts including transformation in soil and honeybee acute toxicity test, the Guidelines adopts relevant OECD test guidelines in terms of the equivalence of basic principles and technical methods, and also incorporates a number of self-developed guidelines, such as "silkworm acute toxicity test" and "macro-crustacean toxicity test".
The Guidelines is mainly used to measure the parameters of environmental fate and eco-toxicity effects of chemical pesticides, in order to provide endpoint data on environmental safety assessment for pesticide regulation and new product research & development.
These test guidelines will take effect on 11 March 2015.It is believed that the release and implementation of the Guidelines will improve the technologies for pesticide environmental risk assessment, reduce the environmental effects of pesticides from the sources, protect ecosystems and advance the development of eco-friendly society in China.
The standard codes and the names of The Guidelines were summarized below:
NO
Standard code
Name
1
GB/T 31270.1- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 1:Transformation in soils
2
GB/T 31270.2- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 2:Hydrolysis
3
GB/T 31270.3- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 3: Phototransformation
4
GB/T 31270.4- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 4: Adsorption/Desorption in soils
5
GB/T 31270.5- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 5:Leaching in soil
6
GB/T 31270.6- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 6: Volatility
7
GB/T 31270.7- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 7: Bioconcentration test
8
GB/T 31270.8- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 8: Degradation in water-sediment systems
9
GB/T 31270.9- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 9: Avian actute toxicity test
10
GB/T 31270.10- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 10: Honeybee acute toxicity test
11
GB/T 31270.11- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 11: Silkworm acute toxicity test
12
GB/T 31270.12- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 12: Fish acute toxicity test
13
GB/T 31270.13- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 13: Daphnia sp. acute immobilisation test
14
GB/T 31270.14- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 14: Alga growth inhibition test
15
GB/T 31270.15- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 15: Earthworm acute toxicity test
16
GB/T 31270.16- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 16: Soil microorganism toxicity test
17
GB/T 31270.17- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 17:Trichogramma acute toxicity test
18
GB/T 31270.18- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 18: Amphibian acute toxicity test
19
GB/T 31270.19- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 19: Effects on non-target plants
20
GB/T 31270.20- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 20: Livestock short-term dietary toxicity test
21
GB/T 31270.21- 2014
Test guidelines on environmental safety assessment for chemical pesticides—Part 21: Macro-crustacean toxicity test
 
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Hi everyone,
I've been interested in spider silk lately. There is a question that puzzle me for a while.
While mainstream papers underlines the advantages of spider silk over other materials (like steel and nylon), few of them mentioned the comparison between spider silk and other insect silks(like silk of silkworm). My question is : is spider silk outperform other insect silk as biomaterial (specially biomaterial for engineering). If yes, how?
Thanks,
Guangqi
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Hey there, Guangqi if you wonder spider silk is far better than the other silks woven by the other insects,you are absolutely correct. Spider silk is so strong that if we this biomaterial is properly used or synthesised we can build a lift which can go to the moon and come back to earth. The strenght of the spider silk is due to it's composition.
The spider silk constitutes of  fibroin (Mr 200,000-300,000) which consist of spidrion 1 and spidrion 2 and 42% glycine and 25% alanine as the major amino acids.
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Mostly cotton fabrics are used in medical field apart from that what is the  main advantages of using silk, polyester or blended silk/polyester fabrics?
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Ideally, silk being a protein fibre, it could be preferred to other fibres for medical textiles to be used in / on the body. But I believe there are better blends of silk with advanced polyesters? Polyester is a generic compound group. If there is clarity on  what polyester, then the listing or answer could be more specific.
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I'm working on wolbachia bacteria to study it's antiviral activities in silk warm cell lines.  However,  I'm not finding the source of bacteria to purchase.  Can anyone help me regarding this? 
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Here I have a link to the World Federation for Culture Collections (www.wfcc.info/index.php/collections/display) with worldwide registrated culture collections. Maybe there is a collection that has your needed strain.
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I have performed uniaxial compression testing for the silk based scaffolds in dry state with varying parameters! The results which i have obtained were less compared to the same test performed for wet scaffolds(reported in a literature). Is there any reason for it?
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yes, the compression test performed under dry and wet state usually show significant differences. that is why researcher prefer to use this test under wet condition to exclude this confounding factor and possible differences, further to simulate the natural body condition. in fact, in the body after implantation, all kind of scaffolds will soaked by body fluid and there is no dry condition except for those implanted externally.
my suggestion is to have both tests (dry/wet) but rely on test result under wet condition. you can use SBF (simulated body fluid at 37 C) to simulate natural condition.
best
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 mainly for  b. mori silk. sericin is a gummy substance which is soluble in hot water. Then why there is need to treat with chemicals like soap solution, sodium carbonate etc.
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Sericin may be in a fairly stable conformation when coating the silk fibers (acting as the "glue" in silk fiber networks). Such stability could arise from the forces between the sericin proteins (like hydrophobic interactions), and just treating with hot water may work but is probably a quite ineffective way to remove all sericin proteins from the fibers. Adding chemicals like various soaps or salts can reduce the interaction between the sericin proteins and yield a more effective denaturing/change of conformation of the sericin, which leads to a more effective removal. 
ATR-FTIR is applicable to most materials that can be analyzed with FTIR in transmission. There are a few studies for how the FTIR spectra depends on the sericin/silk fiber ratio: 
Production of silk sericin/silk fibroin blend nanofibers: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212049/ 
Using FTIR spectroscopy to detect sericin on historic silk: http://link.springer.com/article/10.1007/s11426-010-0050-y
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I am trying it by LiSCN but could not get the proper dissolution.
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5% Caustic Soda solution at cold dissolves silk 
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i am looking for challenges and sustainable solutions in Kenya
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Wild silk farming is prevalent in India But its quantity is very less . There are institutes in India where lots of work in progress to grow and multiply wild silk . Central Institute of technology CSB Ranchi 
CSTRI has come out with reeling and weaving Technology . I am expert in mumberry silk products . You can have alook at my profile on google also 
I have done PhD in Textile technology Silk fabric handle with 22 years of research in Post cocoon Technology with special reference to Mulberry silk I have been trained in Advances is dyeing and printing in Silk Technology  in China Haungzhu university 
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I guess 20X PBS will do this by literature.
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Ionic liquid,  1-Butyl-3-methylimidazolium hexafluorophosphate also do the job -
but don't know what sort of applicaiton you are looking? 
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Tenacity of the silk yarn is one of the important inherent characteristics of the silk yarn   needs to be preserved in processing. Silk is the only filament yarn which is subjected wet   to processing treatment several times  before it is converted into the fabrics Viz Crepe, Georgette Chiffon Taffetta , soft silk  Doupion etc . Each fabric has different handle and lustrous Effect 
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Depends on the type of degumming process.. acid, soap or alkali degumming generally decreases tenacity.. but some degumming chemicals like sodium silicate will not adversely impact tenacity..   this data is at fiber scale. 
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As described that silk mats were sterilized by spraying 70% ethanol. I want to know whether it effects on the activity of growth factor that are co-spun with silk fibroin. Also can we sterilize the mats under UV radiation?
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You can try electron beam (e-beam) sterilization. Probably you will loose some activity of your growth factors but maybe you can start with a higher concentration and  evaluate how much more growth factor you have to co-spun to compensate activity loss. I have done this before with growth factor functionalized silk fibroin films and there was still biological activity after sterilization by e-beam.
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Generally, In silk engineering, we use organic solvents to induce beta crystallinty! I read few papers mentioning autoclaving as a viable technique to induce 60% beta sheet crystallinity which is far better than organic solvents!! May i get the suggestions on the time required to autoclave ,say 3cm X 2 cm, scaffolds to induce secondary structure? Experimental setup, How to autoclave the scaffolds?????
awaiting your kind reply!!!
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Yeah i have found that the autoclaving can be done @ 121 deg C for 20 mins ar 15PSI...
Shall i keep it in a petridish and allow it for autoclaving???? or anyway ????
Thanks
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I work with a fibers of wild silk, fineness 1,07dtex, strength 26,90cN/tex, elongation at break 34,25 CN/tex. In hot water fibers are melt. 
My problem: 200 caterpillar working nest, I need to make insulation of fibers.
Manual isolation is uncertain because it destroys the fiber.
Is there any chemicals (aqueous or oily base) that the fibers would not melt and allowed me the insulation fibers? 
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 Just soften the Silk with Luke  warm water 10 to 25  Degree centigrade. Raw sercin covering fibroin will soften  so that  brittleness is reduced fibers can be handled  
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what are the catalysts required??
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Please, what are the procedures involved in the acetylation of cotton into artificial silk? Edit
what are the catalysts required??
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I have done diaotization of light chain silk for modification of tyrosine present in it. I tried H1-NMR and ATR-FTIR on these modified silk. But no peak was observed, from dizonium salts in both of these characterization, Is there any technique to determine that silk material is diotized and %diaotization done after completion of experiment?  
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I am not sure if this paper describes exactly what you are trying to quantify, but the Kaplan lab has used the extinction coefficient of the azo group to estimate the degree of modification. "Modification of silk fibroin using diazonium coupling chemistry and the effects on hMSC proliferation and differentiation."
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By using plasma treatment on the silk  fiber the Carbon decreases and oxygen increases. Is it hydrophobic or hydrophilic?  
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Dear Jonn Sir,
The paper that u have sent is very useful for me. If u are having any journals related to  plasma treatment on silk ,if it is possible can u share....
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I have seen various articles regarding the major amino acid source is glycine and alanine in case of silk fibroin from B.mori. I would like to know about the possibility of the residual functional groups in the fictionalization of our fibroin with other polymers? Are there any ways?
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Thank you for ur kind concern professor!!!
I mentioned Grafting in the sense??? like functionalisation??? coupling with other proteins or polymers by some chemistry??? 
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I'm trying to measure the porosity of some silk scaffolds I made.  From some papers I read, they did a hexane displacement method to measure the porosity.  Part of the methodology states that they did a quick evacuation-repressurization cycle to completely evacuate the pores from air and replace it with hexane.  Initially, I thought of using the vacuum oven.  However after reading the MSDS of hexane (toxic, flammable), I now have second thoughts of doing this.  Can anyone suggest an easy and safe way of performing an evacuation-repressurization cycle? Is just any vacuum pump compatible with this?
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Considering data for the boiling point of n-hexane at the low vacuum range (760 to 25 mm Hg), you have to deal with the fact that (liquid) n-hexane boils by approx. 121 mm Hg at 20 ºC (taken as room temperature). Cf. J. G. Speight (Ed.), "Lange's Handbook of Chemistry", 16th ed., 2005, McGraw-Hill (Table 2.37).
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I want to soluble completely silk fibroin. Suggest me solvent that will completely solubilize silk.
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We use 9.3M LiBr to dissolve our silk fibroin to make a final concentration of 25% SF in the 9.3M LiBr.  We do this at 60C for 4 hours, as according to David Kaplan's protocol.  To dissolve tougher silk fibroins, you can try higher temperatures or higher concentrations of the LiBr.
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A literature search yields that the size of sericin protein isolated from cocoon of silk worms ranges from 20-400 kDa in SDS-PAGE. The number of bands can be attributed to the reducing effect of SDS, but what is its molecular weight?
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Uniprot suggests that there are three isoforms, one at ca 120 kDa and two around 70kDa. http://www.uniprot.org/uniprot/P07856
The number of bands can't be attributed to the reducing effect of SDS as SDS is not a reducing agent. A high number of bands or smear may be due to incomplete unfolding, or possibly differential glycosylation (if the protein is glycosylated). If isolated from cocoons, I would guess that some degradation may be occurring and you are seeing a range of protein species.
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I am planning to study the surface properties of different types of natural silk fibers by plasma treatment.
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I fully agree to the comments of Emanuel and Bruce. Since silk absorbs higher amounts of water you can also try to use the desorbing water as plasma gas. This works very well with wool which adsorbs similar amounts of water during storage at ambient conditions. At the other side, when a special modification (e.g. plasma-induced hydrophobisation) is desired then you should try to remove most of the adsorbed water from the fibre by predrying.
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If yes, how?
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Hi, it has been successfully done with the genes of Nephila and Araneus spiders, which were transfered into goats, tobacco and Ecoli bacteria. Therefore I don't see why it shouldn't be possible for silk worm genes. But keep in mind these gm proteins only reach 1/3 of the length of natural silk proteins and the main problem is to spin the raw protein into a fiber with compeditive mechanical properties. It seems like only Spiber in Japan is currently capable of making such a fiber. So it should be possible but if it is price compeditive and useful is another.
All the best
Anja
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I am working on silk based small diameter vascular graft, for that I need to stick the inner layer to stick on the mandrel.
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Spider silk
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I'm looking for the very first description of a silk producing Arthropod, most likely it was a spider. Don't get me wrong I'm not looking for a description of a species, we know today it produces silk.
So the very first description people noticed was a "spider" that was producing silk and maybe build a net - something like that.
I hope somebody can help me!
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Dear David,
that's nice thanks a million - love that!
All the best to London,
Sebastian
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LCA is cradle to grave analysis of embodied energy. This is an environmental and energy related topic studied in an inter-disciplinary approach. Textile fibers and textile products attracted early attention, but studies of such kind on silk are rather scarce.
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Many thanks Rajesh, really helpful! I was not aware the production of mulberry was so focused on sericulture in India; I know in China there is significant fruit production, and I thought this would be related to leaf production, but from what you say I gather that trees might be grown for either leaves or fruit?
Good luck with your research on sericulture; if I find something useful I will send it your way!
Kind regards, Llorenc