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Relevant bibliographies by topics / Modified resins

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Academic literature on the topic 'Modified resins'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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Journal articles on the topic "Modified resins"

1

Zhang, Ji Zhi, Xiao Ying Liu, Ying Ying Qiu, Xiao Mei Wang, Jian Zhang Li, and Shi Feng Zhang. "Performances of Modified Urea-Formaldehyde Resins for Bonding Plywood." Applied Mechanics and Materials 71-78 (July 2011): 3170–73. http://dx.doi.org/10.4028/www.scientific.net/amm.71-78.3170.

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Urea-formaldehyde resin was modified by a modifier with different synthetic processes labelled as UFM1, UFM2, and UFM3 respectively. As a comparison, normal UF resin with a F/U molar ratio of 1.1 labelled as UF0 was synthesized. The thermal behavior of modified urea-formaldehyde resins was studied by TG-DTA techniques, and the properties of plywood bonded with the UFM resins were investigated. The conclusions were as follows: (1) the modifier used in this study could significantly reduce the free formaldehyde content of urea-formaldehyde resin and the formaldehyde emission of plywood; (2) The exothermic peak temperatures of DTA curve were 129.37, 125.05, 120.98, and 116.11 °C for UF0, UFM1, UFM2, and UFM3 respectively. (3) The plywood manufactured with UFM2 and UFM3 resins have high bonding strength (1.28MPa and 1.59MPa) and low formaldehyde emission value (E1 grade).

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Yao, Da Hu, Yu Qing Zhang, and Joong Hee Lee. "Increasing Cryogenic Strength of Epoxy Resin Modified by Reactive Macroglycol." Applied Mechanics and Materials 52-54 (March 2011): 2056–59. http://dx.doi.org/10.4028/www.scientific.net/amm.52-54.2056.

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A bisphenol-A glycidol ether epoxy resin was toughened in cryogenic temperature using reactive macroglycol as modifiers. The properties of modified epoxy resin were characterized by SEM and DMA. Phase-separated structure formed during curing process in the PPG and PTMG modified epoxy resins system, and did not occurred in the PEO modified epoxy resins system. The impact strength of epoxy resin increased at both room temperature (RT) and cryogenic temperature (CT, 77 K) using PEO as modifier. The DMA results confirm that the introduction of PEO chains in the structure of the epoxy increases the mobility of the molecular segment of epoxy network at both RT and CT.

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Zhang, Shi Feng, Jian Zhang Li, Ji Zhi Zhang, Yong Hua Li, and Qiang Gao. "Study on Properties of Modified Low Molar Ratio Urea-Formaldehyde Resins (I)." Advanced Materials Research 113-116 (June 2010): 2016–20. http://dx.doi.org/10.4028/www.scientific.net/amr.113-116.2016.

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For improving the performance of urea-formaldehyde (UF) resin, modified low molar ratio UF resins were developed to improve water resistance properties and reduce the formaldehyde emission of its bonded products. The effects of modifier feeding amount on the character of the cured resins were characterized by Fourier transform infrared spectroscopy (FTIR) measurement. The viscosity, pH value, solid content, free formaldehyde content, pot time, and curing time of the UF resins were also tested according to Chinese National Standards methods. The results show that the modified 1.00 molar ratio UF resins show lower free formaldehyde content and higher boiling-water-resistance comparing with unmodified ones. The boiling-water-resistant bonding strength of poplar plywood bonded with modified UF resin at 140 °C hot-press temperature can reach type I grade (100 °C water bath 3h) plywood requirement and the formaldehyde emission can meet the E0 grade plywood need.

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Li, Qi, Xiaosheng Liu, Huidong Su, An Mao, and Hui Wan. "Improving Performance of Phenol-Formaldehyde Resins Modified/Blended with Phenol-Rich Pyrolysis Bio-Oil." Forest Products Journal 70, no. 4 (2020): 387–95. http://dx.doi.org/10.13073/fpj-d-20-00026.

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Abstract In this study, we compare the panel performance of plywood made with phenol-formaldehyde (PF) resins modified and blended with phenol-rich bio-oil produced from pyrolysis of biomass. The modified PF resins were synthesized with phenol-rich bio-oil at phenol substitutions of 10, 25, 50, and 75 percent. The blended PF resins were prepared by blending control PF resin with phenol-rich bio-oil at 4, 13, 23, and 38 percent by weight. These resins were examined with Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) and evaluated as plywood binders. The results indicated that the apparent viscosities of modified PF resins were similar to those of control PF resin, while the apparent viscosities of blended PF resins increased with the addition of phenol-rich bio-oil. As the amount of phenol-rich bio-oil increased, the gel times of both modified and blended PF resins decreased first and then increased. FTIR results showed that modified PF resins with up to 25 percent substitution had FTIR spectra similar to those of control PF resin, while blended PF resins with a higher amount of added bio-oil had spectra more like those of bio-oil. TGA results showed that at temperatures of 25°C to 400°C, both modified and blended PF resins with high bio-oil content had better thermal stability than the control PF resin. Panel tests showed that modifying or synthesizing PF resin with phenol-rich bio-oil up to 50 percent increased both dry and wet bond strength. Blending PF resin with phenol-rich bio-oil up to 13 percent increased both dry and wet bond strength compared with control PF resin.

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Ayrilmis, Nadir, and Günay Özbay. "TECHNOLOGICAL PROPERTIES OF PLYWOOD BONDED WITH PHENOL-FORMALDEHYDE RESOL RESIN SYNTHESIZED WITH BIO-OIL." CERNE 23, no. 4 (2017): 493–500. http://dx.doi.org/10.1590/01047760201723042351.

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ABSTRACT In this study, it was aimed to use of bio-oil as an alternative to petroleum-based phenol in the production of phenol-formaldehyde (PF) resin used for making exterior plywood.Bio-oil obtained from pine wood sawdust using a vacuum pyrolysis reactor at 500 °C. The PF resol resins were produced by substituting up to 20 wt% of phenol with bio-oil by modifying the chemical synthesis process. FT-IRanalysis was performed to characterizethe organic functional groups in the bio-oil modified PF resins. In comparison to the commercial and lab-made PF resins, the bio-oil modified PF resins were found to have larger average molecular weights, higher polydispersity indices, and shorter gel times. Six different types of plywood panels were produced from the experimental PF resins which were commercial PF resin, lab-made PF resin, and PF resins modified with bio oil of 5, 10, 15 or 20 wt% contents, respectively. Plywood specimens produced with the PF resin modified with bio-oil up to 20 wt% had better tensile shear strength (wet condition), modulus of rupture, and modulus of elasticity in bending as compared to the commercial and lab-made PF resins.

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Kizilcan, N., and B. Erson. "Novel phenylacetylene based ketonic resins." Pigment & Resin Technology 44, no. 4 (2015): 198–204. http://dx.doi.org/10.1108/prt-07-2014-0052.

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Purpose – This paper aims to report the synthesis of resins having fluorescence properties, with the help of phenylacetylene (PhAc) by one-step method of in situ modification of ketonic resin. Cyclohexanone-formaldehyde resin (CFR) and acetophenone formaldehyde resin (AFR) were in situ modified with PhAc, in presence of sodium hydroxide (NaOH) by condensation polymerisation. Design/methodology/approach – Ketone, formalin and phenylacetylene were mixed and then 20% aqueous NaOH solution was added to produce the phenylacethylene modified ketonic resin. The solubility, molecular weight and thermal properties of the products were investigated. Findings – These new PhAc-modified ketonic resins (PAc-CFR and PAc-AFR) have fluorescence properties. Research limitations/implications – This study focuses on obtaining a fluorescence resin using a cyclohexanone, acetophenone and PhAc monomer which is an insulator. Practical implications – This study provides technical information for the synthesis of fluorescence comonomers. The modified resins contain acetylene groups. A chemical redox or radical system can be used to polymerise these acetylene groups and resins with much higher molecular weight. The resins may also promote the adhesive strength of a coating and corrosion inhibition to metal surfaces of a coating. Social implications – The resins will be used for the preparation of AB- and ABA-type block copolymers. These block copolymers may exhibit different properties due to incorporation of monomer into the block copolymer structure. Originality/value – PAc-CFR and PAc-AFR have been synthesised in the presence of a basic catalyst. Higher solubility and fluorescence intensity of the modified ketonic resins may increase their applications in the field of electroactive polymers and open new areas. These comonomers have fluorescence property.

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Liu, Wei, Yuxi Zhang, Shui Wang, Lisen Bai, Yanhui Deng, and Jingzhong Tao. "Effect of Pore Size Distribution and Amination on Adsorption Capacities of Polymeric Adsorbents." Molecules 26, no. 17 (2021): 5267. http://dx.doi.org/10.3390/molecules26175267.

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Polymeric adsorbents with different properties were synthesized via suspension polymerization. Equilibrium and kinetics experiments were then performed to verify the adsorption capacities of the resins for molecules of various sizes. The adsorption of small molecules reached equilibrium more quickly than the adsorption of large molecules. Furthermore, the resins with small pores are easy to lower their adsorption capacities for large molecules because of the pore blockage effect. After amination, the specific surface areas of the resins decreased. The average pore diameter decreased when the resin was modified with either primary or tertiary amines, but the pore diameter increased when the resin was modified with secondary amines. The phenol adsorption capacities of the amine-modified resins were reduced because of the decreased specific area. The amine-modified resins could more efficiently adsorb reactive brilliant blue 4 owing to the presence of polar functional groups.

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Tian, Xiu Juan. "Thermal Stabilities and the Thermal Degradation Kinetics Study of the Flame Retardant Epoxy Resins." Advanced Materials Research 1053 (October 2014): 263–67. http://dx.doi.org/10.4028/www.scientific.net/amr.1053.263.

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Thermal stability and thermal degradation kinetics of epoxy resins with 2-(Diphenylphosphinyl)-1, 4-benzenediol were investegated by thermogravimetric analysis (TGA) at different heating rates of 5 K/min, 10 K/min, 20 K/min and 40 K/min. The thermal degradation kinetic mechanism and models of the modified epoxy resins were determined by Coast Redfern method.The results showed that epoxy resins modified with the flame retardant had more thermal stability than pure epoxy resin. The solid-state decomposition mechanism of epoxy resin and the modified epoxy resin corresponded to the controlled decelerating ځ˽̈́˰̵̳͂͆ͅ˼˰̴̱̾˰̸̵̈́˰̵̸̳̱̹̽̾̓̽˰̶̳̹̾̈́̿̾̓ͅ˰̶˸ځ˹˰̵̵͇͂˰̃˸́˽ځ˹2/3. The introduction of phosphorus-containing flame retardant reduced thermal degradation rate of epoxy resins in the primary stage, and promote the formation of carbon layer.

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Kim, Seung Wook, Gae Ho Lee, and Gwi Suk Heo. "Identification of Tackifying Resins and Reinforcing Resins in Cured Rubber." Rubber Chemistry and Technology 72, no. 1 (1999): 181–98. http://dx.doi.org/10.5254/1.3538788.

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Abstract On-line thermogravimetic analysis/Fourier transform-infrared spectroscopy (TGA/FT-IR) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) were employed to identify the tackifying resins and reinforcing resins in cured rubber. Py-GC/MS gave better results in the identification of the resins than the on- line TGA/FT-IR method. The mass spectra of resins in cured rubber were characterized by comparing the mass spectra of the pyrolyzates of raw resins and those of cured rubber containing the resins. t-Butylphenol acetylene condensed resin, coumarone-indene, C5-oligomeric Escorez 1102, modified wood rosin, and reinforcing modified cashew resin were studied. The results show that on-line Py-GC/MS is powerful tool in the analysis of the resins in cured rubber. The diagnostic m/z values of the resins for direct analysis in cured rubber were summarized. Reasonable structural information for resins could be acquired by the characteristic fragmentation patterns.

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Yang, Jie, Xin Mao, Lirong Du, et al. "Thermally stabilized bismaleimide–triazine resin composites for 10-GHz level high-frequency application." High Performance Polymers 30, no. 7 (2017): 833–39. http://dx.doi.org/10.1177/0954008317732396.

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A hybrid cured resin with excellent dielectric and thermal properties was prepared with bismaleimide–triazine (BT) resin modified with 2,2′-diallylbisphenol A (DBA). The thermal and dielectric properties of the resin were investigated, and the effect of DBA concentration on the curing reaction was determined. Results indicated that DBA significantly influenced the curing reaction and the properties of the cured product. The modified BT resins exhibited outstanding thermal stability (initial decomposition temperature was over 400°C), although the stability was slightly lower than that of pure BT resins. The dielectric constant and dielectric loss of the cured resin decreased when DBA was introduced into the BT resins. Moreover, the fabricated resins showed dielectric constant of 2.91–3.07 and dielectric loss lower than 0.0057 under the testing high-frequency range of 1 GHz to 15 GHz. Overall, the BT resins modified by DBA display great potential to be applied in high frequency field.

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Dissertations / Theses on the topic "Modified resins"

1

Zhang, Xiangcheng. "Fracture of modified urethane-methacrylate resins." Thesis, Cranfield University, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358297.

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2

Munshi, Imran. "Reaction-induced phase separation in modified epoxy resins." Thesis, University of Manchester, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493906.

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Studies have been carried out on reaction-induced phase separation in epoxy networks, formed from a DGEBA-type epoxy resin prepolymer, DER332, and m-xylylene diamine, MXDA, containing as modifiers either (i) butyl laurate (B) or (ii) m-cardura (C), (synthesised from Cardura El0 and 2-ethyUiexanoic acid). The reactants and modifiers were characterised using end-group analysis, Fourier transform infra-red spectroscopy (FTIR), differential scanning calorimetry (DSC), nuclear magnetic resonance and viscometry.

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Karad, Sunil. "Moisture sensitivity of cyanate ester modified epoxy resins." Thesis, University of Sheffield, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286617.

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4

Wang, Guigui. "Perfluorotriethylene glycol dimethacrylate modified composite resins for improved dental restoratives." The Ohio State University, 1998. http://catalog.hathitrust.org/api/volumes/oclc/47350511.html.

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Roberts, Karen Narelle 1972. "An investigation of core-shell rubber modified vinyl ester resins." Monash University, School of Physics and Materials Engineering, 2002. http://arrow.monash.edu.au/hdl/1959.1/8416.

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6

Xie, Dong. "N-vinylpyrrolidone modified glass-ionomer resins for improved dental restoratives." The Ohio State University, 1998. http://catalog.hathitrust.org/api/volumes/oclc/47196478.html.

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7

Wu, Jiawei. "Study on Epoxidized Poly (Styrene-butadiene-styrene) Modified Epoxy Resins." University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1571671436341218.

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Thitipoomdeja, Somkiat. "Factors influencing the properties of epoxy resins for composite applications." Thesis, Loughborough University, 1995. https://dspace.lboro.ac.uk/2134/10852.

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The aim of the work reported here was to determine the influence of an amine curing agent, and postcure cycle on the mechanical and thermal properties of diglycidyl ether of bisphenol A (DGEBA) epoxy resin. The results of this initial study were then used as the basis for selecting material to obtain optimum toughness in epoxy/glass fibre systems. These basic materials were further used to make comparisons with the properties of modified resin systems which contained commercial elastomers. Differential Scanning Calorimetry (DSC), Dynamic Mechanical Thermal Analysis (DMTA), Fourier Transform Infrared Spectroscopy (FTIR), flexural and interlaminar shear tests, Instrumented Falling Weight Impact (IFWI), visual observation, Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM) were all used to investigate various properties and the structures which gave rise to them. The properties of cured products were found to be affected by the amounts of curing agent, curing times and temperatures, and the structure of the elastomers. Not surprisingly the maximum thermal and mechanical properties tended to be found in the stoichiometric (standard) mix systems. However, postcuring at higher than room temperature, which was used as the basic curing temperature, led to more conversion. This effect improved the thermal and mechanical properties of both the unmodified and modified resin systems. The maximum flexural strength of 104 MPa of the unreinforced resins was found in the stoichiometric mix ratio after postcure at 150°C for 4 hr. However, the maximum flexural modulus and glass transition temperature (Tg) were found after postcuring at the same temperature for 48 hr. This was believed to be due to increased crosslinking, but unfortunately the longer curing time led to degradation of the resins. In the systems modified with -20 phr of polyetheramine elastomers, the one modified with the lowest molecular weight (2000) was found to have the highest flexural strength (85.8 MPa) and modulus (2.5 GPa). The impact properties of all the composites with modified resin matrices were found to be higher than the unmodified resin matrix composites. The best impact properties were, however, obtained with the elastomer modifier with a molecular weight of 4000. The impact energy at maximum force increased from 11.9 to 16.4 J, and energy at failure increased from 18.7 to 21.6 J. This increase in impact properties was due to the increase in areas of phase separated elastomer particles over similar systems with lower molecular weight modifier.

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Lee, W. H. "Elastomer modified epoxies : Toughening of tetraglycidyl diamino diphenyl methane epoxy." Thesis, Brunel University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234017.

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El-Turabi, Mohammed El Hassan. "The reactions of cellulose and modified cellulose with amide/formaldehyde resins." Thesis, University of Leeds, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329190.

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Books on the topic "Modified resins"

1

Robinson, Thomas Christopher. Optimising damping in HBP modified epoxy resins. University of Birmingham, 2003.

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Conner, Anthony H. Bonding wood veneer with carbohdydrate-modified phenol-formaldehyde resins. Forest Products Laboratory, 1987.

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3

Wilford, Andrea. Structural and Kinetic studies of polysulphide-modified epoxy resins. typescript, 1989.

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4

Morgan, P. The immobilisation of anion exchange resins in polymer modified cements. University of Salford, 1991.

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5

Jokerst, Ronald W. Evaluation of flakeboard bonded with xylitol-modified alkaline phenolic resin. Forest Products Laboratory, 1988.

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Jokerst, Ronald W. Evaluation of flakeboard bonded with xylitol-modified alkaline phenolic resin. Forest Products Laboratory, 1988.

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Jokerst, Ronald W. Evaluation of flakeboard bonded with xylitol-modified alkaline phenolic resin. Forest Products Laboratory, 1988.

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8

Harrison, Anthony Paul. The numerical investigation of a modified Langmuir-type model for moisture absorption in resins. University of Salford, 1988.

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9

Nwokogu, Godson C. Final report on the synthesis of monomers with pendent ethynyl group for modified high performance thermoplastics ... September 1988 to August 31, 1994. National Aeronautics and Space Administration, 1994.

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10

Wilson, Sidney John. The release of chlorhexidine from modified acrylic resin. University ofBirmingham, 1991.

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Book chapters on the topic "Modified resins"

1

Knop, Andre, and Louis A. Pilato. "Modified and Thermal-Resistant Resins." In Phenolic Resins. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-662-02429-4_9.

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2

Gooch, Jan W. "Modified Phenolic Resins." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7580.

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Shaw, S. J. "Rubber modified epoxy resins." In Rubber Toughened Engineering Plastics. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1260-4_6.

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4

Yorkgitis, E. M., N. S. Eiss, C. Tran, G. L. Wilkes, and J. E. McGrath. "Siloxane-modified epoxy resins." In Advances in Polymer Science. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/3-540-15546-5_4.

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Gooch, Jan W. "Resorcinol modified Phenolic Resins." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9978.

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Cook, Phillip M., and Terry Sellers. "Organosolv Lignin-Modified Phenolic Resins." In ACS Symposium Series. American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0397.ch024.

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Abdollahi, Hossein, Ali Samadi, and Somayyeh Hosseini Rad. "Toughening Mechanism of Polyetheramine-Modified Epoxy Resins." In Eco-friendly and Smart Polymer Systems. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-45085-4_92.

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Castaldo, Rachele, Francesca De Falco, Veronica Ambrogi, et al. "Modified Hyper-crosslinked Resins for Textile Wastewater Treatment." In Springer Water. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-45909-3_43.

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Conner, Anthony H., Linda F. Lorenz, and Bryan H. River. "Carbohydrate-Modified Phenol-Formaldehyde Resins Formulated at Neutral Conditions." In ACS Symposium Series. American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0385.ch025.

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Ho, Tsung-Han, and Chun-Shan Wang. "Polysiloxane Thermoplastic Polyurethane Modified Epoxy Resins for Electronic Application." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0614.ch035.

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Conference papers on the topic "Modified resins"

1

Ozeki, Shinichi. "Modified Phenolic Resins for High Performance Friction Applications." In 19th Annual Brake Colloquium And Exhibition. SAE International, 2001. http://dx.doi.org/10.4271/2001-01-3127.

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2

Pissis, P. "Dielectric and hygrothermal studies in rubber modified epoxy resins." In Seventh International Conference on Dielectric Materials, Measurements and Applications. IEE, 1996. http://dx.doi.org/10.1049/cp:19960990.

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Barra, Giuseppina, Luigi Vertuccio, Carlo Naddeo, Maurizio Arena, Massimo Viscardi, and Liberata Guadagno. "Thermal degradation and fire properties of epoxy modified resins." In 9TH INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2018. http://dx.doi.org/10.1063/1.5046011.

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Bershas, James P., and Russell H. Tobias. "The Use of Modified Unsaturated Resins In Structural RRIM Composites." In SAE International Congress and Exposition. SAE International, 1988. http://dx.doi.org/10.4271/880430.

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Pawlowski, Georg, Thomas P. Sauer, Ralph R. Dammel, et al. "Modified polyhydroxystyrenes as matrix resins for dissolution inhibition type photoresists." In Microlithography '90, 4-9 Mar, San Jose, edited by Michael P. C. Watts. SPIE, 1990. http://dx.doi.org/10.1117/12.20135.

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Mandowski, Arkadiusz, Ewa Mandowska, P. Czub, W. Mazela, Jozef Swiatek, and Jan Pielichowski. "Kinetic analysis of long-lived luminescence in modified epoxy resins." In SPIE Proceedings, edited by Jaroslaw Rutkowski and Antoni Rogalski. SPIE, 2003. http://dx.doi.org/10.1117/12.519676.

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Shields, Nigel, and Philippe J. Sabat. "New Modified Dow Polyamide Resins Solving Under-the-Hood Warpage Problems." In International Body Engineering Conference & Exhibition and Automotive & Transportation Technology Congress. SAE International, 2002. http://dx.doi.org/10.4271/2002-01-2104.

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Komiya, Gen, Ken-ichi Yamazaki, Takahiro Imai, et al. "Development of epoxy resins modified with lignocellulosic biomass for insulating materials." In 2011 International Symposium on Electrical Insulating Materials (ISEIM). IEEE, 2011. http://dx.doi.org/10.1109/iseim.2011.6826398.

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Hu, Bing, Liming Zeng, Chuanqun Hu, and Dongbing Meng. "Study on Improvement of Thermal and Mechanical Properties of PEEK-Modified Epoxy Resins." In 2006 7th International Conference on Electronic Packaging Technology. IEEE, 2006. http://dx.doi.org/10.1109/icept.2006.359780.

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Shu, Peter H. C. "A High Speed Impact Study of Impact-Modified Polycarbonate Resins for Instrument Panel Applications." In SAE International Congress and Exposition. SAE International, 1988. http://dx.doi.org/10.4271/880500.

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Reports on the topic "Modified resins"

1

Ting, Robert Y., Aver A. Shaulov, and Wallace A. Smith. Piezoelectric Properties of 1-3 Composites of a Calcium-Modified Lead Titanate in Epoxy Resins. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada235934.

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Morris, John B. Chemically modified polymeric resins for separation of cations, organic acids, and small polar moleculea by high performance liquid chromatography. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10116711.

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Schmidt, L. W. Chemically modified polymeric resins for solid-phase extraction and group separation prior to analysis by liquid or gas chromatography. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10116845.

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Nuttall, Christopher S. Bond Strength of Silorane- and Methacrylate-Based Composites to Resin-Modified Glass Ionomers. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ad1013158.

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Kessler, Michael R., and Prashanth Badrinarayanan. Cyanate Ester Resin Modified with Nano-particles for Inclusion in Continuous Fiber Reinforced Composites. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada562120.

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