Fred Adler wrote: > > I am hoping that someone can give me some insight into the chemical > nature of the ordinary transparency films used in laser printers > and/or photocopiers. > (snip) > Fred Adler (snip) As far as I know, "acetates" are actually made from PET (Mylar etc) nowadays. I don't think they are coated. Shouldn't be too hard to find out who extrudes them. 3M make a range of them. Michael.Return to Top
In article <32860D7C.9E@winewall.demon.co.uk>, adrian@winewall.demon.co.uk says... > >This is a multi-part message in MIME format. > >--------------138F57E9594B >Content-Type: text/plain; charset=us-ascii >Content-Transfer-Encoding: 7bit > >-- >reply to ds3eng@bolton.ac.uk >Davinder Sandhu > >--------------138F57E9594B >Content-Type: text/plain; charset=iso-8859-1; name="cai.txt" >Content-Transfer-Encoding: 8bit >Content-Disposition: inline; filename="cai.txt" > >I am currently in the middle of a project to build an impact test rig to carry out >compression-after-impact tests on composite materials. I would like to hear from >anyone who has carried out similar tests so that I may compare my results with theirs. >Similarly if anyone knows of any web sites that have information on this area and in >particular the related failure theorems, I’d like to hear from you. I’ve found a few but >none that allow you to view their results. > >--------------138F57E9594B-- > This is an interested question with a number of variables. CAI will depend, of course, on the type of composites you have and what you're trying to learn from the testing. (Damage tolerance vs. damage resistance, maybe GIIc) There's also a big difference between fabric composites and unidirectional laminates. I did some CAI tests on RTM laminates I made for my master's thesis. These were conducted on 65mm square specimens impacted with a horizontal gas gun. My purpose was to see the effects of resin or sizing on the fiber, using both carbon and glass fabrics. After impact, the damage is measured by ultrasound (the accuracy of which is questionable) and a smaller compression specimen is cut from the whole,I think 25.4mm by 40mm, I'll have to check. There are a few standards also out there for CAI. Among these is a Boeing Standard and some dead weight drop tests. Anyway, hope this'll help. You might try to reach someone at Virginia Tech dept. of Engineering Science and Mechanics at http://www.vt.edu. Hope thiss'll help. Email if you want more info on the compression test. I should have something lying around. Rob Demaree rdemaree@scsn.net ThereReturn to Top
Polyurethane foams are mode by taking an isocyanate and reacrting it in the presence of water. The isocayanate group reacts with water to form an amine and carbon dioxide-which causes the bubbles which cause the foaming. Eventually, other isocyanate groups will react with the amine groups, which then trap in the faom structure. There are several technical articles about the process (look up "polyurethanes" in the Encyclopeida of Polymer Science and Engineering Ed. By Mark, Menges, Overberger, et. al.) However, most of the foams are made by the Bayer chemical company (which makes the isocyantaes-water , of course, is free.) Look up their Web Page for a possible tutorial. Cynthia Donahey wrote: > > How is polyurethane foam made? > What materials are used? > Is there any limit to size? > Besides being an absorbent, what else can it be called? in order of > importance. > > I have been cutting out out old cushions and using them as planters with > some real interesting and practical results. One of the strangest things > about these planters is the place where soil and the foam meet. The soil > seems to slide away from the foam. So do plants, although they will climb > over nicely. I still don't know if roots will grow through this material. > Some basics would be appreciated. -- Brent D. Viers Department of Chemistry Polymer Research Center Mail Location 0172 University of Cincinnati Cincinnati, OH 45221-0172 Telephones: 513-556-9291 513-556-9290 Fax: 513-556-9239 e-mail:viersbd@ucbeh.san.uc.eduReturn to Top
I am interested in information on coupling agents for silica loaded into epoxies, such as Shell EPON 805 or 815. Trade name, company and other contact information would be greatly appreciated. TomReturn to Top
!! world premiere !! From november 11th, the Fructan Page proudly presents the world's first virtual reality Fructans. Now you can see them in a 3D world and actually walk toward them twist them around and just be amazed at what's possible these days. I hereby invite everybody for a visit to the Fructan Page. You won't be sorry. If you don't know what fructans are yet, there's plenty of information on this subject at The Fructan Page. The Fructan PageReturn to Top
I am trying to locate poly(N-isopropylacrylamide) PNIPAM. This polymer is a thermo-sensitive polymer. Does anyone know of a company selling this material. Any and all help would be greatly appreciated.Return to Top
I would really like to get some commercial information on coating interior and exterior surfaces of pipe. Thanks, TonyReturn to Top
Jerry P. Solomon wrote: > > Can anyone suggest a reference for abrasion resistance of various > plastic materials. Initially, I am interested in UHMWPE, TFE, and > other fluorocarbon compounds. > > My address is: JPSOLO@CCMAIL.MONSANTO.COM > > Thanks in advance for any advice. > > Jerry Solomon > Monsanto Company Please call Technicoat, Inc. at 201-568-3337. Regards, Alec Ganopolsky Tecnnicoat, Inc. http://www.finishing.com/technicoatReturn to Top
Anyone knows what acryloid's/Acrylic Ester Resins are? What are they used for? Suppliers? If you can't help me, maybe you have an suggestion for another specialised newsgroup? Thanks BasReturn to Top
X-Article-Creation-Date: Tue Nov 12 00:09:59 1996 GMT X-Originating-IP-Addr: 207.76.102.135 () X-Authenticated-Sender: dsmall@pcisys.net Lines: 24 Xref: magma.Mines.EDU sci.polymers:8568 sci.chem:72393 In article <3276FD4A.3C51@greenepa.net>Return to Top, Wayne Goates wrote: > > I have a T-shirt that will change color from a more or less drab gray > color to that of a blue and a yellow when exposed to the UV light of the > sun. Does anyone know what company markets this Thermochromatic product > and if so, what is their address? Thanks in advance. > ---------- > Wayne Goates Email:goat5200@spacelink.msfc.nasa.gov > Wayne, The T-shirt you're referring to is Photochromic (UV light sensitive)-- not Thermochromic (Heat sensitive). My company, Chromatic Technologies, Inc., (www.lightlink.com/cti/) offers both these types of inks, as well as finished products, like T-shirts and other promotional products. If you would like further info., please call us at (719) 592-1557. - Danny ----------------------------------------------------------------------- This article was posted to Usenet via the Posting Service at Deja News: http://www.dejanews.com/ [Search, Post, and Read Usenet News]
X-Article-Creation-Date: Tue Nov 12 00:09:59 1996 GMT X-Originating-IP-Addr: 207.76.102.135 () X-Authenticated-Sender: dsmall@pcisys.net Lines: 24 Xref: magma.Mines.EDU sci.polymers:8568 sci.chem:72393 In article <3276FD4A.3C51@greenepa.net>Return to Top, Wayne Goates wrote: > > I have a T-shirt that will change color from a more or less drab gray > color to that of a blue and a yellow when exposed to the UV light of the > sun. Does anyone know what company markets this Thermochromatic product > and if so, what is their address? Thanks in advance. > ---------- > Wayne Goates Email:goat5200@spacelink.msfc.nasa.gov > Wayne, The T-shirt you're referring to is Photochromic (UV light sensitive)-- not Thermochromic (Heat sensitive). My company, Chromatic Technologies, Inc., (www.lightlink.com/cti/) offers both these types of inks, as well as finished products, like T-shirts and other promotional products. If you would like further info., please call us at (719) 592-1557. - Danny ----------------------------------------------------------------------- This article was posted to Usenet via the Posting Service at Deja News: http://www.dejanews.com/ [Search, Post, and Read Usenet News]
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I have been struggling with a project involving styrene-vinyltoluene copolymers. The polymer is made via emulsion polymerization with sodium lauryl sulfate as an emulsifier. The procedure I was given calls for coagulation with salt water to get a powder. The powder must then be washed with deionized water to wash out the sodium. This washing used a great deal of water and requires many cycles (at least 12) to get the sodium content down to below 500 ppm. Any suggestions on improving this washing? What swelling agents can I use to improve the washing step? I suspect the polymer particles shrink and trap the salt inside the particle. Thanks for your help! alchemist@fyi.netReturn to Top
In article <55dpuh$fti@newsbf02.news.aol.com> mioxirane@aol.com (Mioxirane) writes: >I have just finished reading an article about electron beam curing of >epoxy materials.The concept seems pretty simple. Just pass a stream of >high energy elecrtrons through your systme to cure your material. > >The article says that for successful e-beam curing, the resin systems must >be modified. To become e-beam curable the systems should contain a >cationic photo-initiator. What materials would be cationic >photo-initiators for this type of systme described?? This article >appeared in the September/October issue of High-Performance Composites. There are many options, but one simple (and very effective) example is Ph3S(+)AsF6(-) (TPS AsF6; triphenylsulfonium hexafluoroarsenate) in conjunction with glycidylnovolaks. This class of salts generates a superacid (HAsF6) upon exposure to actinic radiation (e-beam, x-ray, deep UV) which then catalyzes cationic polymerization of the epoxide moieties. Tony GozdzReturn to Top
In article <55omaj$d0q@hermes.louisville.edu> skshah01@starbase.spd.louisville.edu writes: >Just wondering if anyone might have some rate constants for phenol >formaldehyde polymerization. Well, there are so many options for this _condensation_ reaction, and people have been studying it for the past 60 years... Tony Gozdz tony2@bellcore.comReturn to Top
In article <327E0253.2991@starnetinc.com> heisel19@starnetinc.com writes: >Polyethylene containers are surface treated with fluorine gas to improve >their solvent barrier properties. I am looking for a quantitative test >to determine the extent of conversion of C-H bonds to C-F bonds. FTIR >may have some potential. Any suggestions would be welcome. Usually, XPS/Ar+ beam sputtering or SIMS are the methods of choice for such surface-composition studies. Then come ATR IR, contact-angle measurements, RBS... Tony Gozdz tony2@bellcore.comReturn to Top
In articleReturn to Topwrites: > >Brian, >We are currently applying for a patent to cover silicone bonding and >coatings on polyester materials, and a smililar process should work well >on PBT. [...] Various silicone-coated PET films are also commercially available from many distributors. DuPont, amongst others, makes several grades. Tony Gozdz tony2@bellcore.com
In article <327D6E87.F73@cris.com> Ralph &/or DonnaReturn to Topwrites: >Michael Thompson wrote: >> >> I am writing a term paper on ionomers in general and PE ionomer and its >> properties/processing specifically. Unfortunately, there does not seem to >> be much printed material about ionomers. Any direction is greatly >> appreciated (e-mail contacts, web pages, databases etc) >> >> Thanks in advance. > >Primacor(r) resins are commercially available ethylene/acrylic acid >resins from the Dow Chemical Company. > >czere@dow.com > or the well-known Surlyn(tm) from DuPont. BTW, the original poster's claim about the dearth of printed material on ionomers cannot be taken too seriously... A quick search of several publicly accessible patent databases (e.g., http://www.qpat.com) will show why. I don't even venture to guess how many thousands of entries would be found in Chemical Abstracts (unfortunately, not a freebe). Tony Gozdz tony2@bellcore.com
To whom it may concern: I have some questions regarding polymers and I am uncertain how to source an answer. If my questions enter into your field of expertise, and you can be of some assistance, please respond to my e-mail (any assistance or referrals you can be provided would be incredibly beneficial). The company I own manufactures golf course yardage markers out of recycled tires. It has been fairly successful but over this last summer some weaknesses with our products have surfaced and we are having problems addressing the problem. The markers we make are 15" hectagons, approx. 2" thick. The major problem we have experienced is with golfers kicking them as a result of "golfing frustrations". The recycled tire component "crumbles" under consistent impact. We have been attempting to rectify the situation by covering the recycled tire component with a material of a similar flexibility but more resistant to abuse. The application we have attempted is a two part polyurethane poured (transfer molded ?) into a mold the same size as our yardage marker. We then pull the polyurethane part out of the mould (or tool) and glue it onto the yardage marker. The moulded polyurethane is useful in that we can incorporate golf course logos onto our product whereas before it was difficult to do with our recycled tire component. We are finding the polyurethane to be too expensive, but because we use it as our bonding agent for the recycled tires, we are somewhat familiar with it and were able to source it out. Through my research (to date) I have found that a polymer such as PVC or EPDM may work well in our application but I am uncertain if another polymer can be applied in the moulded application I have described. Briefly, here are questions I am looking to have answered: 1. Is there other polymers than can be poured into molds such as the ones I have described? (transfer moulded) 2. Would a suitable polymer be UV stable and retain our common colours of red, white, yellow, blue and black over an extended period of time? 3. Would a suitable polymer be resistant enough to withstand golf-cleat traffic? 4. Would a suitable polymer be cheap enough to incorporate into our product? (cheaper than an aromatic polyurethane) 5. Would a suitable polymer be effected in anyway by golf course chemicals? (fertilizers, pesticides etc.) 6. Would a suitable polymer be flexible or have a hardness of 70A - 90A? As you may have guessed, I am not a chemist nor do I have any knowledge of polymers. I am in desperate need of assistance and finding that up here in Canada there are very few people able to offer me any useful information. As mentioned, if you can provide me with any information, it would be greatly appreciated. Hoping to here from you soon, Todd Weimer P.S. Because my company deals with recycled products, we like to keep the recycled content as high as possible. A best case scenario for a polymer would be one that could use, I have been informed, "thermoset polymers" as inert fillers. Its "GreeK" to me but I understand it as adding a recycled polymer component to virgin polymer (am I correct in this and is it possible?).Return to Top
To whom it may concern: I have some questions regarding polymers and I am uncertain how to source an answer. If my questions enter into your field of expertise, and you can be of some assistance, please respond to my e-mail (any assistance or referrals you can be provided would be incredibly beneficial). The company I own manufactures golf course yardage markers out of recycled tires. It has been fairly successful but over this last summer some weaknesses with our products have surfaced and we are having problems addressing the problem. The markers we make are 15" hectagons, approx. 2" thick. The major problem we have experienced is with golfers kicking them as a result of "golfing frustrations". The recycled tire component "crumbles" under consistent impact. We have been attempting to rectify the situation by covering the recycled tire component with a material of a similar flexibility but more resistant to abuse. The application we have attempted is a two part polyurethane poured (transfer molded ?) into a mold the same size as our yardage marker. We then pull the polyurethane part out of the mould (or tool) and glue it onto the yardage marker. The moulded polyurethane is useful in that we can incorporate golf course logos onto our product whereas before it was difficult to do with our recycled tire component. We are finding the polyurethane to be too expensive, but because we use it as our bonding agent for the recycled tires, we are somewhat familiar with it and were able to source it out. Through my research (to date) I have found that a polymer such as PVC or EPDM may work well in our application but I am uncertain if another polymer can be applied in the moulded application I have described. Briefly, here are questions I am looking to have answered: 1. Is there other polymers than can be poured into molds such as the ones I have described? (transfer moulded) 2. Would a suitable polymer be UV stable and retain our common colours of red, white, yellow, blue and black over an extended period of time? 3. Would a suitable polymer be resistant enough to withstand golf-cleat traffic? 4. Would a suitable polymer be cheap enough to incorporate into our product? (cheaper than an aromatic polyurethane) 5. Would a suitable polymer be effected in anyway by golf course chemicals? (fertilizers, pesticides etc.) 6. Would a suitable polymer be flexible or have a hardness of 70A - 90A? As you may have guessed, I am not a chemist nor do I have any knowledge of polymers. I am in desperate need of assistance and finding that up here in Canada there are very few people able to offer me any useful information. As mentioned, if you can provide me with any information, it would be greatly appreciated. Hoping to here from you soon, Todd Weimer P.S. Because my company deals with recycled products, we like to keep the recycled content as high as possible. A best case scenario for a polymer would be one that could use, I have been informed, "thermoset polymers" as inert fillers. Its "GreeK" to me but I understand it as adding a recycled polymer component to virgin polymer (am I correct in this and is it possible?).Return to Top
I am looking for information on what I call coilcoating, but in fact I have no idea whether that is the proper word. What I mean is the lamination of sheet metall with a film. This film is as far as I know a laminate, PET/adh./s-PVC laminate. The laminate is bonded to the metall using a solvent based PU adhesive. Does anybody no more? More detail on the adhesive, how is the adhesive applied, both adhesives applied at the same time, does anybody know other laminate constructions for this application, is the bonding of s-PVC without problems, what is the plasticiser in s-PVC, how is the film caoted on the metall etc.etc. All info is very much appreciated. BasReturn to Top